SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs62015177 | snp | A/C | 0.208779 | 0.246578 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750429 | TGAATCATAGCATCT[A/C]GGAAAGGAAGGATTG | 5607 |
rs62015178 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750818 | GTTGGGATTTGAGCC[A/G]TTTTACTGCTTGGGA | 5607 |
rs62015179 | snp | C/T | 0.18134 | 0.240387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751085 | AAGGTGGGCAAGAGC[C/T]AGTCCTGGAATGGCC | 5607 |
rs62015181 | snp | A/G | 0.206642 | 0.246211 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752256 | ATTATTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 5607 |
rs62015182 | snp | C/G | 0.199254 | 0.244796 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752542 | AATGAGCCGAGCCGG[C/G]TGGCAGGCACCTGTA | 5607 |
rs62015183 | snp | C/T | 0.199254 | 0.244796 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752609 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 5607 |
rs62015184 | snp | A/G | 0.157642 | 0.232314 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752782 | TCTCAAAATTGATCT[A/G]CAGATTCAATGTAAT | 5607 |
rs62015185 | snp | A/G | 0.199254 | 0.244796 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753049 | AACTTATATATGCAT[A/G]GTCAGTTGTTTTCTG | 5607 |
rs62015187 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759250 | GATTGCCTAATAATA[C/T]CTCCCAGAAATTCAA | 5607 |
rs62015188 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764142 | GGTTTAATCCAACCA[A/C]AGTACAGCTGACCTC | 5607 |
rs62015212 | snp | A/G | 0.182614 | 0.240747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770720 | CACTATGATCTGTCC[A/G]ATGATTATGCTAAAG | 5607 |
rs62015213 | snp | A/G | 0.22263 | 0.248497 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773427 | TAATAATTATAGTCT[A/G]TTCTTTCTAATGTTT | 5607 |
rs62015215 | snp | G/T | 0.157972 | 0.232445 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778948 | ATGTAGTTCACTACA[G/T]TTAGGTATTGCCTGT | 5607 |
rs62015216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779711 | ATGTCTCTAATGCCT[C/G]TTTCGTGTTTTATTG | 5607 |
rs62015217 | snp | A/G | 0.158302 | 0.232576 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780653 | AGAATACATGGCCAG[A/G]TAAAAAAGGTTTTTG | 5607 |
rs62015218 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783637 | GAGACCACAACCCCT[C/T]GAGGAAGAGATCATG | 5607 |
rs62015219 | snp | C/T | 0.155325 | 0.23138 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784667 | GGTCTGTTAGTTGGT[C/T]ATCTGAGGGGAAGCT | 5607 |
rs62015220 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786572 | TGGCTTGGGTGGTGC[A/G]GGAGCTCGGAACAGT | 5607 |
rs62015221 | snp | C/G | 0.029116 | 0.117091 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788763 | AGGATCACTTTCGCC[C/G]AGGAGTTCGAGACCC | 5607 |
rs62015222 | snp | C/T | 0.15665 | 0.231917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789913 | AGGGGGTGGACACAA[C/T]TTCCAAGGCCCCATC | 5607 |
rs62015223 | snp | A/G | 0.177503 | 0.239258 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792874 | AGCTTGTCTGTCCCC[A/G]TGAGATCACATGGTG | 5607 |
rs62015224 | snp | C/T | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794297 | GTTCTTTGTGTTTTG[C/T]TTTAGAAAATATTGC | 5607 |
rs62015225 | snp | A/T | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796017 | TTGTTGATATTAATA[A/T]AGCTATGCCATCTTC | 5607 |
rs62015227 | snp | A/G | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801471 | GCAGTCCTGTGGTCC[A/G]GAGAGCCACCAAATG | 5607 |
rs62015242 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805601 | CTGGAGGGAGGAGAG[A/C]GCTGGGGGGAGCGAG | 5607 |
rs62016160 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596737 | TCAGTGCCAGTCATT[C/T]CTCTAAGGTCATTTG | 5607 |
rs62016161 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599885 | TAATTGTATAGGGAG[A/C]TCTCTAAACTCTAAA | 5607 |
rs62016162 | snp | G/T | 0.147991 | 0.228242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601457 | AAAATATTCCACTAG[G/T]AATTAAAAAATCCAT | 5607 |
rs62016163 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608425 | GTCAGATGTTGGGGA[C/T]AGCCTAGCCTCATAA | 5607 |
rs62016164 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609470 | CTATAGGTCTATAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs62016175 | snp | C/T | 0.040671 | 0.13668 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618847 | TTTTACTGCAAAAGC[C/T]TCCCAACTAGCCTCC | 5607 |
rs62016177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627541 | TGGATAAGTATATAC[A/G]TATGCTTTATATATG | 5607 |
rs62016178 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628434 | GTGGTGAGCCAAGAT[C/T]GTGCCACTGCTCTCC | 5607 |
rs62016179 | snp | A/G | 0.18134 | 0.240387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628937 | TGGAAGCAATTTTGG[A/G]GGTGGTGGAAGCTAC | 5607 |
rs62016180 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630205 | TGCCACTGTGTTCCA[A/G]CCTAGGTGTCAGAGA | 5607 |
rs62016181 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633282 | TTTTTGTTCCTTTTA[C/T]GTCAGAAGTCTTAGA | 5607 |
rs62016182 | snp | A/G | 0.273856 | 0.248859 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637642 | CTCCAGGACCCCCTC[A/G]GCAGACCTCTGGAGC | 5607 |
rs62016184 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637932 | TGTGAGTGTGTGTGT[A/G]TGTGTGTTTTAGTAC | 5607 |
rs62016185 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638379 | CCTCCAGCTCCATCC[A/T]TGTTCCTGCAGAGGA | 5607 |
rs62016186 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638541 | TGACCATTTGCATGC[A/G]TGTGTCTTTATAATA | 5607 |
rs62016188 | snp | A/G | 0.153997 | 0.230832 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643878 | TTCCTTGCTCTATTA[A/G]CAGTTTATAATGCAT | 5607 |
rs62016195 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645553 | TGATCACAAACCACA[A/G]GATAGTTCTTTTTTT | 5607 |
rs62016196 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647824 | CAGTGAACCAAGATC[G/T]CGCCACTGCACTCCA | 5607 |
rs62016197 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649664 | CTTTCAGATCAATGC[A/G]TATACATCTCGCATT | 5607 |
rs62016198 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652899 | TATTTGTCTTATTGT[A/G]TCTGGCTTATTTCAT | 5607 |
rs62016199 | snp | A/G | 0.154329 | 0.23097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654458 | AGACAGCATATAGTT[A/G]GATCATTTTTTTAAA | 5607 |
rs62016200 | snp | A/G | 0.228547 | 0.249078 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656702 | CATCAGCTGACTCAT[A/G]GCTTTAGCTAGAACA | 5607 |
rs62016202 | snp | A/T | 0.0333308 | 0.124718 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664676 | ATAAGCTTGGATTTA[A/T]TTTGGGGTGGGGTTG | 5607 |
rs62016203 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668204 | GTTTTTATTATAACC[A/G]TGAATTAATCACTTT | 5607 |
rs62016204 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668811 | TACACAGATGCAGAA[A/G]TTTATAGAAGAAAAA | 5607 |
rs62016207 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672308 | TTCCTATTTCTCTAC[A/G]TCCTCTCCAGCACCT | 5607 |
rs62016220 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682455 | ATTTCGATCTCCTGA[C/T]CTCATGTTTCACCCG | 5607 |
rs62016221 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682464 | TCCTGATCTCATGTT[C/T]CACCCGCCTTGGCCT | 5607 |
rs62016222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694822 | CACGTATGTTTATTG[C/T]GGCATTATTCACAAT | 5607 |
rs62016223 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694881 | CCAACAATGATAGAC[A/T]GGATTAAAAAAATGT | 5607 |
rs62016224 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694932 | TACTATGCAGCCATA[A/C]AAAATGATGAGTTCA | 5607 |
rs62016225 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705902 | AGAGAGACCAGTGTG[A/C]CTTGACTGGAGTTAA | 5607 |
rs62016226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707194 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGAC | 5607 |
rs62016227 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710829 | GATTTTTTGGGCTCT[A/G]TTATTTTGACAAAAA | 5607 |
rs62016228 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712583 | GCTGCTGTAACAAAA[A/G/T]GAACTTTCAGAGAAC | 5607 |
rs62016229 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714470 | ACCACCACCCTGACA[C/G]AGCTGTTTCTAATGG | 5607 |
rs62016230 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714583 | TCTGTAAGCAGCTGC[C/T]GTCAACTTTTCCACA | 5607 |
rs62016231 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715809 | AAAGCCAAAAAAATA[A/G]TAAACTCCCATGACT | 5607 |
rs66480531 | snp | A/G | 0.226779 | 0.248919 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633479 | TATTAAAAGTATTGT[A/G]CATTAGTTGGGTGTG | 5607 |
rs66482647 | snp | A/G | 0.25045 | 0.25 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696075 | TATTATAGTACAGGT[A/G]TGAATCCCTGACTTT | 5607 |
rs66548496 | in-del | -/A | 0.278133 | 0.248412 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693383 | TTTTATTGCCTTTGT[-/A]GATAAATTTGTTCCC | 5607 |
rs66616278 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632112 | TTTTTTTTTTTTTTT[-/TT]TGATTGAGACAGGGT | 5607 |
rs66634396 | in-del | -/A | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696128 | AAAAAAAAAAAAAAA[-/A]GCTCAGCTCTTTTCT | 5607 |
rs66760415 | snp | A/T | 0.252983 | 0.249982 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653445 | CACCCAGCTACTCTG[A/T]GCCACCATGCCCTGC | 5607 |
rs66818657 | snp | A/G | 0.251296 | 0.249997 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708153 | AGACTCCATCTCTAA[A/G]AAAACAATTTTTTTT | 5607 |
rs66877651 | snp | A/G | 0.264358 | 0.249587 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636456 | ATAACTGAATTAGTG[A/G]CCTTATCTATTTATT | 5607 |
rs66976874 | in-del | -/CTTTCTTT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575920 | TTTCTTTCTTTCTTT[-/CTTTCTTT]CTTTTTTTTTTTTTT | 5607 |
rs67100731 | snp | C/G | 0.252421 | 0.249988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686723 | AGTGATTTACCAAAG[C/G]CTGGGGGTCAGGGTA | 5607 |
rs67180939 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784785 | TTCTGCCTTTCCACT[CT/TC]TGCCATCATGGGTAT | 5607 |
rs67260432 | snp | A/G | 0.226484 | 0.248892 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667800 | GTGGTCCAGATTTTA[A/G]CTATAGAAAGTGTAT | 5607 |
rs67264405 | snp | C/T | 0.264084 | 0.249603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631486 | AATCACAGATCTGAC[C/T]GTGTCTTGCTGACTG | 5607 |
rs67356187 | snp | C/T | 0.25214 | 0.249991 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633757 | ATTTAAGAGCAGATA[C/T]GATTATTGTGATTAA | 5607 |
rs67507836 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585077 | TCTGAGAGAGGAGCA[-/A]AAAAAAAAAAAAAAA | 5607 |
rs67575262 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780285 | CCAGGGAGCAGATAC[-/T]TTTTTTTTTTTTTAA | 5607 |
rs67607106 | in-del | -/A/AA | 0.625 | 0.125 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632113 | GACCCTGTCTCAATC[-/A/AA]AAAAAAAAAAAAAAA | 5607 |
rs67821440 | snp | A/G | 0.252702 | 0.249985 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633837 | ACTTGTATAATAGTC[A/G]TAATCTAAGAAAAAT | 5607 |
rs67864219 | snp | C/T | 0.263809 | 0.249618 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634621 | ATATTCTTAGGTGCA[C/T]TTATGTTTGTTATGT | 5607 |
rs67999453 | in-del | -/GCGGCGACGGCGGTAGCGGCG | 0.413914 | 0.188765 | utr-variant-5-prime, cds-indel, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542722 | GCGGCGGCTGCGGCG[-/GCGGCGACGGCGGTAGCGGCG]AGAGGAGGAGGAGGA | 5607 |
rs68152622 | snp | A/G | 0.25801 | 0.249872 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694433 | ATGGATAAAACCGTG[A/G]GTCTTAGTCTCAGTA | 5607 |
rs71142378 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553942 | CTTCTCAACTATTTC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs71142380 | in-del | -/T | 0.163892 | 0.234703 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569006 | TGTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 5607 |
rs71142381 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575936 | CAAGACTCCATCTTA[-/A]AAAAAAAAAAAAAAA | 5607 |
rs71142382 | in-del | -/TAAGAG | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580535 | CCTGGCATTTATCTT[-/TAAGAG]TAAAAGTGTTGATTA | 5607 |
rs71142383 | in-del | -/TG/TGAGAG/TGAGAGAGAG/TGAGAGAGAGAGAGAGAGAGAG | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590468 | GAAACAAAGAGAGAG[lengthTooLong]AGAGAGAGAGAGAGA | 5607 |
rs71142384 | in-del | -/TTTTT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592135 | ATTTAGTGAAAGTCC[-/TTTTT]TTTTTTTTTTTTTTT | 5607 |
rs71142385 | in-del | -/CAGAATCTACAGACCTATAGAATAGGTCTACAGAATCTACAGACCTATAGAATAGGTCTACAGAATCTACAGACCTATAGAATAGGTCTA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609505 | TATAGAATAGGTCTA[lengthTooLong]CAGAATCTATAGACC | 5607 |
rs71142388 | in-del | -/CACACACACACA | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624628 | TCCGTCAAACACACT[-/CACACACACACA]CACACACACACACAC | 5607 |
rs71142389 | in-del | -/A | 0.323434 | 0.238972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624797 | CTAAAAATACAAAAA[-/A]TTAACCAGGCCTGGT | 5607 |
rs71142390 | in-del | -/TTTTTTTT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634402 | GTGGATTATACATTC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 5607 |
rs71142392 | in-del | -/GAGGTTGCAGTG | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648646 | GTGGAGGTTGCAGTG[-/GAGGTTGCAGTG]AGCCGAGATCACCCC | 5607 |
rs71142397 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763659 | AAATCGAGTTTGTTT[-/A]AAAAAAAAAAATCTA | 5607 |
rs71142398 | in-del | -/ACACACAT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774167 | CACACACACACACAC[-/ACACACAT]ACACACACATCACTT | 5607 |
rs71209392 | multinucleotide-polymorphism | GC/TT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701171 | AAAAAAGGACAGGGG[GC/TT]AGGGCAGCATTTAGT | 5607 |
rs71287012 | in-del | -/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655079 | AGTTTTTGTATACTA[-/T]TTTTTTTTTTTTTTT | 5607 |
rs71400372 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585899 | TTTCAGCCTGCAAGC[C/T]TCCTGGGGAACGGAA | 5607 |
rs71400373 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631162 | TTGCCAAGAAGAGAA[A/G]ATTTCTTTCTGTGTC | 5607 |
rs71400374 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663931 | AAAAAAGTTTTACAC[A/C]CAGAAGTATAGAAAA | 5607 |
rs71400375 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686369 | CCCAGCACTTTGGGA[A/G]GCCAAGGCAAGCAGA | 5607 |
rs71400376 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697526 | ATTTATGCATCTCCC[C/G]CAATCTAGATTATGA | 5607 |
rs71400377 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714216 | AATATATTCAATATT[C/T]TAGGCTTTTTCATGA | 5607 |
rs71400378 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774175 | AAGTGATGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs71409162 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609620 | CTATAGGTCTATAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs71455556 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541874 | AAAAAAAAAAAAAAA[-/A]GATAACCAAGGTTTA | 5607 |
rs71455557 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575921 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs71455559 | in-del | -/A | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582664 | GTCTCTACCAAAAAA[-/A]TACAAAAATTAGCCG | 5607 |
rs71455560 | in-del | -/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650938 | CATTTTAGGGGCTGG[-/G]ACAGGGTGGCTCACG | 5607 |
rs71455561 | in-del | -/A | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704765 | TTTCAGGGGAAACTA[-/A]GTGTTTTTGATTTGT | 5607 |
rs71455564 | in-del | -/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776213 | CCCCACCCCCACCCC[-/C]ACCTCCACTTCTGCC | 5607 |
rs71941187 | in-del | -/TGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589784 | ATGTGTGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 5607 |
rs72106715 | in-del | -/CACACACA | 0.267091 | 0.249415 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711672 | ACACAGGCGTGCACG[-/CACACACA]CACACACACACACAA | 5607 |
rs72106781 | in-del | -/TGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774168 | AGTGATGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 5607 |
rs72132989 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737868 | GGAATAGAATAGTCT[-/TT]TTTTTTTTTTTTTTT | 5607 |
rs72327832 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599697 | TGATTTTTTTTTTTT[-/TT]TCAGGGCTTGCAGTG | 5607 |
rs72343244 | in-del | -/CACACACA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711686 | GCACACACACACACA[-/CACACACA]AAAGGATAATACCAT | 5607 |
rs72417540 | in-del | -/CGCGCCG | 0.00398564 | 0.0444627 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542536 | ACTCGCCACGCGCCA[-/CGCGCCG]CGCGCCGCGCGCCGG | 5607 |
rs72417910 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594755 | TATGGCTTTTTTTTT[-/T]CTTTATAAGGATTAG | 5607 |
rs72747493 | snp | C/T | 0.238749 | 0.249747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544251 | GAAAAAAATGCTAAC[C/T]ATGACAGTATGACAC | 5607 |
rs72747499 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552143 | CTATTGTTTGAACAT[A/T]TTTCAACAATCATTG | 5607 |
rs72749315 | snp | C/T | 0.238749 | 0.249747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564664 | AATTTAGAGCTGGGC[C/T]CATCAGTACCTTGAA | 5607 |
rs72749319 | snp | C/G | 0.239326 | 0.249772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565807 | TAGAGATAGGGTCTT[C/G]CTTTGTTGCCCAGGT | 5607 |
rs72749325 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570540 | ATATTCAAAATAGAT[G/T]GGCTTCATATGTTAT | 5607 |
rs72749331 | snp | C/T | 0.237593 | 0.249692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578747 | AAAATGAAAGGAAAA[C/T]CATTTTTATTTATTT | 5607 |
rs72749337 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582059 | GGATGTAGATGATTT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs72749348 | snp | C/G | 0.255224 | 0.249945 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596442 | CAACAACAGGAAAAC[C/G]TTTTTGTATATAGAA | 5607 |
rs72749351 | snp | A/G | 0.257176 | 0.249897 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598642 | TTCCCTGTAGTGGAT[A/G]TAAGTGGTAAAAAGA | 5607 |
rs72749353 | snp | G/T | 0.23846 | 0.249734 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599415 | ATTGGTAAAATGGCT[G/T]GGAAAAGAAGCTGTT | 5607 |
rs72749359 | snp | A/G | 0.239037 | 0.24976 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608865 | TTGTGTTCCCTGGAG[A/G]AGAGTCATGTCTAGG | 5607 |
rs72749364 | snp | C/T | 0.239326 | 0.249772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612600 | GTCGTTCAGTTTTTA[C/T]GTTAAAGGAAAAAGT | 5607 |
rs72749372 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622225 | GTAGGAAAGTCAAAG[A/C]AACAATATAGGACCT | 5607 |
rs72749380 | snp | C/G | 0.239614 | 0.249784 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627791 | AAAATTTTGTCAGTC[C/G]TTTCTGCTCGTGGAC | 5607 |
rs72749383 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634150 | GATGACTTGAGCTCA[A/G]GAGTACGAGACCAGC | 5607 |
rs72749392 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657817 | TTTTTACAGATAAAA[A/G]TATTTTCTCTGATGT | 5607 |
rs72749397 | snp | A/G | 0.252702 | 0.249985 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673263 | GTTGCAAAAAAATGC[A/G]CAAGACAGTCCCATC | 5607 |
rs72749398 | snp | C/T | 0.252702 | 0.249985 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673264 | TTGCAAAAAAATGCA[C/T]AAGACAGTCCCATCT | 5607 |
rs72751407 | snp | A/G | 0.253544 | 0.249975 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681652 | AAACCTTAAATTAGG[A/G]AACACCTAAACTTGA | 5607 |
rs72751410 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696248 | TCTCAGGCCAAATTC[A/G]ATTTACTGGAACAAT | 5607 |
rs72751413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713758 | AAAAAAAGTGGCATG[A/G]ATCACCCAGCCCAGT | 5607 |
rs72751415 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720609 | CGTAAAGGTACTAAT[A/G]CCTGAGGGGTGGGTC | 5607 |
rs72751419 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724134 | GAAACACATTTAGTA[C/T]AGTGACATATCTGCA | 5607 |
rs72751427 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733519 | ATTGGGAAAAAAAAA[A/T]ACCATCATCTGGCCA | 5607 |
rs72751428 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734559 | ACTTAATTTTATTTG[A/T]GTTTTAAAAGCCTTT | 5607 |
rs72751429 | snp | C/T | 0.224709 | 0.248717 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734972 | TAATTCATTTTACTT[C/T]TGTCCTCACTATTTA | 5607 |
rs72751443 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792409 | TCTTTGGGGCTACCA[A/G]GACTTGAAAAATGTT | 5607 |
rs72751444 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795453 | CTTCAATTCTAAGTA[A/G]TTTTCAATTTCAATT | 5607 |
rs72751447 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799586 | TTACTTCTATACAAA[G/T]CTGGATTGGAGGATG | 5607 |
rs72751449 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804714 | GACACTGTGTTACCC[C/T]GGGCGTGGGGGGAGG | 5607 |
rs73423889 | snp | G/T | 0.301681 | 0.2446 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674171 | TTTTTAAAAGAACTG[G/T]TTAGTGCTTGAGTAA | 5607 |
rs73425906 | snp | C/T | 0.305934 | 0.243663 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682514 | AGGTGTGAGCCACTG[C/T]GCCTGGCCCCTGGAG | 5607 |
rs73425917 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687276 | ATTGGTTTCTGGTTC[A/C]ATAAGTCTGGAGTAG | 5607 |
rs73425958 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703947 | TGTGTATGTGGGTTA[A/G]GGGGTGGTGTGATAT | 5607 |
rs73425961 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703988 | GAAGGGGGAAGAGGA[C/T]GTATGTATTTAGCAC | 5607 |
rs73425997 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726120 | ATATCTTGAAAATCC[A/G]TACACATATCAGTGT | 5607 |
rs73427924 | snp | C/T | 0.117886 | 0.21224 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741630 | GGTGAAGTCATCTTC[C/T]CATGGAACACACGGG | 5607 |
rs73427929 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746437 | GAATGTAGGGGTGGG[A/G]GGAGTATCAGTGTGT | 5607 |
rs73427943 | snp | C/T | 0.235273 | 0.249566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751676 | TTGGCAGCCTGTTGA[C/T]GGAGTGTGGTGAATA | 5607 |
rs73427944 | snp | A/G | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753092 | AGACCATTCTGTGGC[A/G]AAAGAATAGTCTTTT | 5607 |
rs73427948 | snp | A/G | 0.226779 | 0.248919 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755003 | TTGAGATGGAGTCTT[A/G]CTCTGTTTGCCCAGG | 5607 |
rs73427958 | snp | C/G | 0.25912 | 0.249834 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758838 | CTTACATTATACTAT[C/G]ACTGATTTGAAGAAA | 5607 |
rs73427960 | snp | A/G | 0.258843 | 0.249844 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759270 | CAGAAATTCAAAAGC[A/G]GGGTTAGGCCAGGCA | 5607 |
rs73427984 | snp | C/T | 0.214843 | 0.247516 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771208 | ACCATGTGTTTTACA[C/T]ATGGTAATGCCTCAT | 5607 |
rs73427991 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778408 | GCTTCACACCAAATG[A/G]CTTTGTTTCATTGTT | 5607 |
rs73433619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560212 | GCATTTTTGCTTTAC[A/G]GGTTAAGGTGAGTGG | 5607 |
rs73433641 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589204 | GAACATGCAGATGAA[C/T]GAAATATTGAGTAAA | 5607 |
rs73441617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608959 | GTGTTTCAGGAATTT[A/G]CCTGCAGAGGCAGAT | 5607 |
rs73441671 | snp | C/T | 0.27278 | 0.24896 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635224 | AGAGTCTCGCTCTGT[C/T]GCCTAGGCTGGAGTG | 5607 |
rs74020405 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681727 | AAAGGTTTATGTGTT[A/G]CGGTAGAAGAAACTT | 5607 |
rs74020409 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703723 | ATTGTTAACCTGTTC[C/T]CTGGGTGATTCTTAT | 5607 |
rs74020410 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706683 | AACTATAGGATTGTA[A/G]CCCCTGACCTCTAGG | 5607 |
rs74020411 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711686 | GCACACACACACACA[A/C]ACACACAAAAGGATA | 5607 |
rs74020414 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731496 | AACTTCCTTGGCATG[C/T]AGTTTAGGGTTCTAA | 5607 |
rs74020415 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747583 | TGTTGATCAGAAATG[C/T]GCTCTTACTGGACTC | 5607 |
rs74020421 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773060 | GAATTCAGAGGATTG[C/G]TAACAGAAGATCATC | 5607 |
rs74020422 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773755 | GATCACCCCTAAAAA[A/C/T]CTCTGCAATTTATAA | 5607 |
rs74020425 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805472 | GTGGCGAGGCCATGC[A/G]GCTCTTTAAGCAGCC | 5607 |
rs74023012 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577460 | CTGAAGATGAAGTTA[G/T]TTGGATAACTTGAAG | 5607 |
rs74023013 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577464 | AGATGAAGTTATTTG[C/G]ATAACTTGAAGTAAT | 5607 |
rs74023015 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592347 | TAATTTTTCTGGTTA[C/G]CCTATAAAATTGGTA | 5607 |
rs74023018 | snp | C/G | 0.175254 | 0.238565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605847 | GGGGCTCTTTCATTG[C/G]ATCTTCCTCATATCT | 5607 |
rs74023019 | snp | C/T | 0.292523 | 0.246357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605903 | GTTGTAGAACATTCA[C/T]CTAGAAGAAAAAGAA | 5607 |
rs74023020 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612771 | AAAGTAAATAAATGA[A/G]TGGACAGCAATCACA | 5607 |
rs74023022 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643088 | TTCCATTGTTTTGGG[G/T]TAAAGCCTGCACCTT | 5607 |
rs74208934 | snp | G/T | 0.438946 | 0.163706 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756576 | GTTGATAACACTTAC[G/T]ATCTACTCCCTTGGC | 5607 |
rs74328121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687432 | ATACATAAACAACAT[C/T]GTTATCCTAAAATCG | 5607 |
rs74343832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779384 | GCTTTAATTTGAATT[C/T]TTGATGACACATTAG | 5607 |
rs74351479 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603879 | ATGAAGAAAATATTG[G/T]AAAATCCACTCATTG | 5607 |
rs74354975 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655891 | CAGGTCTCCGAGAAT[A/G]TGTTCATTTTTCTTC | 5607 |
rs74358564 | snp | C/T | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738141 | ACAGGCGTGAGCCAC[C/T]GCACTTGGCCTAGAA | 5607 |
rs74358924 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662620 | TATAGCAATTTATAC[A/G]TAAAGATTTTTTAAG | 5607 |
rs74409681 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699142 | AGTTTTTTTTTTTTT[-/TT]AAACCATCTCAAATG | 5607 |
rs74423105 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766634 | TCCCTCCTCACAGAT[G/T]TGAATTAGATAACAA | 5607 |
rs74426868 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727406 | TTTTTCCCACTAGTG[A/G]GTAGAAAATGGATGA | 5607 |
rs74433077 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776843 | CATCACATCCCTTCA[C/G]TGTGTAACCTCAGCC | 5607 |
rs74450654 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555801 | TTTCCTTTTTTTTTT[G/T]GAGACGCAGTCTCAC | 5607 |
rs74569532 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620414 | ACTGATAAAGTATAT[A/C]CCTGTGAATTTAAAT | 5607 |
rs74603813 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624639 | TGTGTGTGTGTGTGT[A/G]AGTGTGTTTGACGGA | 5607 |
rs74604735 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800802 | TACGTCCTAAGTGGA[C/T]GTCTTTTTTCAAATG | 5607 |
rs74649903 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648589 | GTTCTTTTTTTTTTT[G/T]TGAAACAGAGTCTCG | 5607 |
rs74651334 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575596 | TGAGGTATGAGAAAT[A/C]TGAGATAACCTACTT | 5607 |
rs74653509 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548913 | CACAGATTTATTTTT[A/G]AAAAAAAAAAAAAGC | 5607 |
rs74749516 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588986 | ATCCCTGATTAAGTG[G/T]TTTTTTTTTATTTTT | 5607 |
rs74754776 | snp | A/C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789716 | GCAAAACTCTGTTTC[A/C/G]AAAAAAAAAAAGGAT | 5607 |
rs74755819 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718144 | GAATATCAGCTGTTT[A/C]TGACTCCCTTGACTT | 5607 |
rs74762309 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798146 | CCCCATATTCACAGT[A/G]TGGACATGCTGCAGA | 5607 |
rs74780666 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745183 | AAAACACTCAACACA[C/T]GCAAAATGTATAAGC | 5607 |
rs74813999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693160 | CTAGTAATGCATGGG[A/G]CTTCATTCACATCTT | 5607 |
rs74838217 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701701 | AATTATTTTTTAAGT[A/G]AGGATCTCTAGCCCC | 5607 |
rs74845260 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780041 | CTTTTCCCTACTCTT[C/T]GACTTTACAGTTGCT | 5607 |
rs74873919 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638241 | CAACACACACTGGGC[C/T]TTTCAGAAGGTGGAG | 5607 |
rs74937538 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602782 | CCTCAGCCTCCCAAG[C/G]AGTTGGGATTACAGG | 5607 |
rs74945137 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761757 | AAGATCAATTTTTTT[C/T]CATTTAGGCACCTAT | 5607 |
rs74947916 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711848 | AGGAATTGGTGGGAC[A/G]AGATATGTGGAGCCA | 5607 |
rs74994179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627554 | ACATATGCTTTATAT[A/G]TGTAGTTTCCTAGTC | 5607 |
rs75009351 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714296 | GCCTTTTGAAATAGC[A/G]TCTTATATGTATTGA | 5607 |
rs75010760 | snp | A/G | 0.161924 | 0.233971 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749598 | TAAACACACACACAC[A/G]TATCACAATAATAGT | 5607 |
rs75019401 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667663 | AGAGTAAAAAAAAAA[A/G]GAAATTGCTTTGTAC | 5607 |
rs75060737 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605071 | TTTCTTTTTTTTTTT[G/T]GAGACAGAGTCTCGC | 5607 |
rs75067831 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722354 | TAATTTGTAACTCTT[C/T]TTTTTTTTTTTTGGT | 5607 |
rs75075787 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655534 | CTTTCATGTTCAAAT[A/G]TCATTCCCCTGCCTC | 5607 |
rs75083417 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676324 | TTGGATGAATACATT[C/G]AATCATAATTTTCTG | 5607 |
rs75085775 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706010 | AAGGACTTTAGGTAT[G/T]ACTCTTAGAAGAAAT | 5607 |
rs75119190 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612073 | TTTATCTTTGGTTTT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs75124995 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780272 | CCAGGGAGCAGATAC[-/TT]TTTTTTTTTTTTAAC | 5607 |
rs75130324 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772518 | TTACTCATAATGTCC[A/C]CCAGAAATCTGACTA | 5607 |
rs75136536 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545786 | GTGAAAGTAATGCCT[A/G]CCTCCTAGAGTTCTG | 5607 |
rs75143213 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730101 | TTTTCAACAGAAGTT[G/T]GGGTGCGTCGTTGCT | 5607 |
rs75162941 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616318 | ATAATTGAACCTGAG[C/T]GAGACCAACTCTTAA | 5607 |
rs75202691 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770452 | TCCAGCACAGAGAAT[C/T]ACCTAGGAGAGAGGA | 5607 |
rs75215691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711046 | CACCTGCATCTTCCT[G/T]GTGGCATGTAAATTG | 5607 |
rs75231680 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696132 | AAGAGCTGAGCTTTT[C/T]TTTTTTTTTTTTTAA | 5607 |
rs75244541 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740595 | GAGACCCTGTCTCAA[A/C]AAAAAAAAAAGTGTT | 5607 |
rs75250330 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643114 | ACCTTGGGATTTTTT[C/T]CAAGTGCCCTAGGTA | 5607 |
rs75257134 | in-del | -/CAAAAAAAAAAAAAAAAAAAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634367 | AGTAAGACCTCATCT[-/CAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 5607 |
rs75264663 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570000 | ACAGCCTAAAAATCA[A/G]GTGAAAGGTCAGTGT | 5607 |
rs75277053 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741350 | CTAGTCTTCCTTGCT[A/G]GTTTTAGCTGGGACT | 5607 |
rs75279692 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626153 | GATGTGGAGGGGGAA[A/G]AATAATATATCACAA | 5607 |
rs75283379 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777522 | TCCTTTGTAGCATGC[A/G]CTTCGGCTGTGGTAA | 5607 |
rs75292390 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696131 | AAAGAGCTGAGCTTT[C/T]TTTTTTTTTTTTTTA | 5607 |
rs75300062 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737573 | GAAAAAATCAATGAG[C/T]TGCCTAAAAGGAGCA | 5607 |
rs75307597 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600104 | AAGTGCATTGATTTC[A/G]TGCTTTTCCATCTTC | 5607 |
rs75332797 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750529 | CCTCATAGGGTGGAC[C/G]AAGGACTGATTGCAT | 5607 |
rs75404305 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795757 | GTTTCTCAAATATTT[C/G/T]GTGGCTGTACTAATT | 5607 |
rs75431516 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575765 | TAGAATAGGATAGGA[C/T]TGTAAAAAACTAAGT | 5607 |
rs75433729 | in-del | -/T | 0.296873 | 0.245566 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547113 | ACACACACACACAGA[-/T]TTCTGTCTAAACTGA | 5607 |
rs75465979 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719738 | CTCATCTGTTGCAAC[A/G]TCTCAGATTCCAGAT | 5607 |
rs75466172 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635908 | TATCACTGGTATTGA[A/G]CTGGTGTTTACATCT | 5607 |
rs75473171 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611615 | AATGTAGCTGAGCAC[A/G]CTAGGTATCGTCATC | 5607 |
rs75492855 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748925 | ATGATATCATTTTTT[C/T]CTGCAACAGTTATTT | 5607 |
rs75529498 | snp | C/T | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796464 | ATCACATGGCAAAAA[C/T]ATAGGCAAGAGAGAC | 5607 |
rs75642147 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668148 | GGTTGAGATATATGT[A/G]CAGGGACTTTATAAA | 5607 |
rs75649656 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558270 | GAATGCATGGATGGT[G/T]GAAGAGTGAAGTAAT | 5607 |
rs75650546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733303 | TTTAAGCTGTTTTTA[A/G]GAATTATTTGAATAA | 5607 |
rs75654503 | snp | A/G | 0.210301 | 0.246828 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733790 | AGATAATAAGTGAAA[A/G]ATATGCATTCTTAAT | 5607 |
rs75682215 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791588 | GCTGCTATTATATTG[C/T]ACATCATCACAAAAG | 5607 |
rs75691645 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772584 | TAATACTTTGGCCAA[G/T]AATTGAACATGATGT | 5607 |
rs75717846 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782905 | TTCCTGCCTTCAGAA[A/C]CGGCCCCCTTTTCAG | 5607 |
rs75718946 | snp | C/G/T | 0.0150714 | 0.0855845 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597295 | CTTCTTAAAAACTAA[C/G/T]ATCGTAGCTAATGAA | 5607 |
rs75728180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792628 | AATATAAAACTTCCC[A/G]CTGAGTTTCTGAGTC | 5607 |
rs75741662 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775918 | AAACAGGCAACATAT[G/T]CACCACCAGCTGGGC | 5607 |
rs75747832 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745928 | ACAAAATTTATGAAG[A/G]TGATTTCATATAATA | 5607 |
rs75776721 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801633 | TGCCACATAATATCA[A/G]GCTTCCTAGAGCTTT | 5607 |
rs75797388 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755415 | TATTAGCTGCCCCTT[A/G]GTCTGCCTGACTCAC | 5607 |
rs75802821 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605072 | TTCTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 5607 |
rs75812824 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588476 | TAGTAGTGAGCACAT[A/T]GTATTATAATCACCC | 5607 |
rs75819977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720815 | TTTGCTGGAGTAATA[C/T]TCCAGGATGATTTAT | 5607 |
rs75844848 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786020 | TAGCTGTTAGGTTGT[G/T]TTTTTTTTTTTAACT | 5607 |
rs75879550 | snp | A/G | 0 | 0 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542542 | CACGCGCCACGCGCC[A/G]CGCGCCGCGCGCCGG | 5607 |
rs75908100 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703228 | TTTGTCATCCGTAAA[A/G]TACTATGCAGATGTT | 5607 |
rs75944494 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603705 | GATATAATCATTGAT[A/G]AATGAGGATCCACTT | 5607 |
rs75964174 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653300 | ATATTTTTTTTTTTT[G/T]TTGAGACGGAGTTCT | 5607 |
rs76003799 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784263 | CAGGACTGTCCTACT[A/G]CACAACATCAAAGCT | 5607 |
rs76005918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718466 | ACTCTAATCATTTTT[A/T]AAAAATTTTTATGGG | 5607 |
rs76014331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802346 | CAATGTCCCTCATTG[G/T]GCTTCTCAGCCCTGT | 5607 |
rs76037830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701635 | GTCTCTCCAGGGAAC[A/G]TGGAAATATTTAGTG | 5607 |
rs76056522 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701666 | ACTGGAGCTAAGTGT[A/G]CCAAAGAATCACCCA | 5607 |
rs76087241 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682163 | GTTGTCTATGGCTTC[A/G]AGTGAAGCTGAAAAC | 5607 |
rs76087665 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549563 | GTTTATGTTTATTAG[A/G]TTAATTTTTAAGCTA | 5607 |
rs76092511 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752909 | ATTGAAAAAAAAAAA[-/AA]GAAAACAATGTTGCA | 5607 |
rs76092950 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733639 | TGCCAGCTTTTGCCA[A/C]CAGTGTACAAAATAG | 5607 |
rs76106150 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632113 | TTTTTTTTTTTTTTT[G/T]GATTGAGACAGGGTC | 5607 |
rs76109387 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599605 | GTCTGAGAGCAAACT[A/T]TTTTTTTTCCAAGTG | 5607 |
rs76119580 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701704 | TATTTTTTAAGTGAG[A/G]ATCTCTAGCCCCACC | 5607 |
rs76120825 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745093 | AATGCAACTAGTTCT[A/G]GAGACTGATTAACAA | 5607 |
rs76164701 | in-del | -/GA | 0.499998 | 0.000998401 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805596 | GGAAGCTGGAGGGAG[-/GA]GAGAGCTGGGGGGAG | 5607 |
rs76191425 | snp | C/T | 0.15698 | 0.23205 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790477 | GTCTGAGGGCACTGC[C/T]GTCTTGTCTGTAGGC | 5607 |
rs76203356 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635838 | TCATTTTAAATCTTT[A/G]TTCCTCTGTATATTA | 5607 |
rs76234783 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571488 | TACTTTGTCCAGATA[G/T]CTCAGTCGCCTTGTT | 5607 |
rs76237523 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603509 | TTTTCATTCTTATAT[A/G]GTAGATTTCTTATAA | 5607 |
rs76259574 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644800 | GACTGGAAAAAAAAA[A/G]GATGATATATTTTTA | 5607 |
rs76269222 | snp | A/G | 0.029116 | 0.117091 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787020 | GATGGGGTAAAGTTA[A/G]CTGCATGGGGCCAGT | 5607 |
rs76272694 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568256 | AAGTGTAAGTATTCC[C/G]TTTGGTGTATTTGAC | 5607 |
rs76273412 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585094 | AAAAAAAAAAAAAAA[A/T]ATCAAATTAATTCGT | 5607 |
rs76285731 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740067 | TATTTTGTCCAAATA[A/C]TGAGTGACTTTTAGA | 5607 |
rs76330848 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659263 | GTCTAAGAGAAGTCA[G/T]GGGGTGGTGTGATAG | 5607 |
rs76345937 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650257 | TATACAAGATAATGC[C/T]ATCTGCAAATAGAGG | 5607 |
rs76424386 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616186 | AAATAAAATGTCACA[A/C]AGAGCAAAGAAGCAT | 5607 |
rs76430838 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674482 | TGAAAAGAAAAAAAA[A/G]GACTTAGCCCATTAA | 5607 |
rs76449377 | snp | C/G | 0.237593 | 0.249692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582152 | CCGCAACCTCTGACT[C/G]CCTGGTTCAAGTGAT | 5607 |
rs76453530 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607539 | TTGGCATCCAGCCAA[C/G]ATGACAGGATGTCAC | 5607 |
rs76456746 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761032 | AGATTCCAAACTGGT[C/T]GGCTGGGGTGTTGCC | 5607 |
rs76476531 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651762 | CTTTATTTTTTCTTC[A/G]ATGGACACTCAGATT | 5607 |
rs76488680 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782911 | CCTTCAGAAACGGCC[C/G]CCTTTTCAGCTCTCC | 5607 |
rs76489741 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749707 | TAAAAATGAAGGCAT[C/T]GTCCTGAAACAAATG | 5607 |
rs76491044 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721281 | TGGTAGATAAGTGCT[G/T]GATTTATTTATTTGT | 5607 |
rs76511969 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597031 | ACAATTAGCTGGGCA[C/T]GGTGGTGGGCGCCTG | 5607 |
rs76512152 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555802 | TTCCTTTTTTTTTTT[G/T]AGACGCAGTCTCACT | 5607 |
rs76549626 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805352 | TGTGGTCCAGAGGGG[A/C]CATGCCGTCCCCTGC | 5607 |
rs76577408 | snp | C/T | 0.0236746 | 0.106192 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807492 | CCTCACTGCCCTTGA[C/T]CCCACACCTGCCACC | 5607 |
rs76589548 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796879 | GACATTCAAGCTCCA[G/T]CCAGCAGGAAAGGAG | 5607 |
rs76595566 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681310 | TTATGAGAATTAAGT[A/G]AAATTGTGTGCTCAA | 5607 |
rs76616765 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711407 | GCCTAAGCTATAGAA[C/G]CTTCGGTAAATTACT | 5607 |
rs76628078 | snp | C/T | 0.226188 | 0.248863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743540 | AGCCAGAGTAAATTT[C/T]GTTCTCTTCCTTTAT | 5607 |
rs76632880 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669155 | CTACTACGTTCTAGG[C/T]GCTTTCACAGTACTT | 5607 |
rs76646754 | snp | A/G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746466 | GTGCTTGAAAAAAAA[A/G/T]TAAAAGCAAACTCCA | 5607 |
rs76660402 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746246 | ATAATCCATTTCTGA[A/G]TTCATTTCAAAACCT | 5607 |
rs76669450 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588985 | AATCCCTGATTAAGT[G/T]TTTTTTTTTTATTTT | 5607 |
rs76684414 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730312 | ACACCTTCTCTTTGG[A/C]CCACGTTATGTCATT | 5607 |
rs76759946 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626140 | TGGAAGAATCTGTGA[C/T]GTGGAGGGGGAAAAA | 5607 |
rs76772885 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621922 | GGTGCGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 5607 |
rs76798815 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798156 | ACAGTGTGGACATGC[C/T]GCAGACTCCACCTTT | 5607 |
rs76849377 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705444 | ATGGAGGAAAAAAAA[A/G]GCAGACTAGGCTGGG | 5607 |
rs76857879 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640524 | TGTCACAGAGGATTG[C/T]GAAGAGCAGCAAATC | 5607 |
rs76877183 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784284 | CATCAAAGCTACACC[C/T]GTTGTTGCATAGTAG | 5607 |
rs76902971 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792440 | GCTCTGTATCAAGAA[A/C]ACCAGAAGTGACAAG | 5607 |
rs76918703 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647102 | AATCTAAGCAGTCTT[C/T]AAATTTTACATATTC | 5607 |
rs76940545 | snp | C/T | 0.0752113 | 0.178743 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718478 | TTTAAAAAATTTTTA[C/T]GGGGGCTGGGTGCAG | 5607 |
rs76970675 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744548 | GAGAAAATGAAAGCT[A/G]TAGCTGGTGTCTTCT | 5607 |
rs76976915 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551841 | AATTCAAAGCATTCA[A/G]CAGTGACTAAAAAGA | 5607 |
rs77042257 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587914 | TGCGTCTTTCTACTC[A/G]CCAGCATCCCTGCTG | 5607 |
rs77104559 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675704 | CTTAATGTAAACAAC[A/C]AAAAAAGAATATATC | 5607 |
rs77106422 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782285 | TTAAGTATTAGTAAT[C/T]GGGAGATTAGGGCCC | 5607 |
rs77108230 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615403 | TGAACTAGTATAGTT[C/T]ACATAAAAGCTTCTT | 5607 |
rs77109780 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666790 | AAGATATCTGTTGGG[A/G]ACACAGTAGGAACAG | 5607 |
rs77130374 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567616 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 5607 |
rs77143808 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779212 | CTGACAACCATGGAA[A/T]TTTTTTTTAAGTTCT | 5607 |
rs77148098 | snp | A/G | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783360 | CTCCTGTGGAGTCCT[A/G]TGCTCCAAACTTCTG | 5607 |
rs77159434 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701618 | AGATGTAAAAGGTCA[G/T]TGTCTCTCCAGGGAA | 5607 |
rs77178181 | snp | C/T | 0.000391489 | 0.0139854 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806871 | TGGCTTCCCTGCCCT[C/T]GCCTTCACCTCTGTC | 5607 |
rs77182350 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709000 | AGATGTAACAAAAAG[A/T]TGGAAGTTATCCTTA | 5607 |
rs77215417 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635204 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 5607 |
rs77238438 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756179 | TTTTAAGTATCATAT[G/T]CATTCCAAATGAACT | 5607 |
rs77271670 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622402 | GTGAGGTAACTAACC[A/G]GGGCCCAGATGTTGA | 5607 |
rs77274143 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700939 | TTCTTCTTAAATTTA[A/G]TTTAATTTTTCTATG | 5607 |
rs77384416 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635966 | ACTTCCTCTGCTTTC[C/T]TTTTTTTTGTTTTTA | 5607 |
rs77392032 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683300 | GCTGTCCTTAACCCA[A/G]GATTTAAAGGGATTC | 5607 |
rs77496529 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730605 | CACAGGGTCAAAGCA[A/G]TGTTCTATTTATCAA | 5607 |
rs77575909 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635969 | TCCTCTGCTTTCTTT[C/T]TTTTTGTTTTTATAA | 5607 |
rs77576072 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679223 | GCTCTTGAGGCTCTG[A/G]CCTTTATTAGCAAGC | 5607 |
rs77577252 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597185 | AAAAAGAAAAAAAAA[A/G]GAAAAAAAAAAACTA | 5607 |
rs77596380 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756256 | GGCAACATTTTCTCT[C/G]TCTCACCATCTTCTT | 5607 |
rs77597298 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712404 | ACTCTTACAGAGACA[C/T]TTGAGAAAGGCCTTT | 5607 |
rs77612763 | snp | C/T | 0.170733 | 0.237101 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789057 | CATATCTTCCAGCCC[C/T]AATCTCTAGAGATAA | 5607 |
rs77623453 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714302 | TGAAATAGCATCTTA[C/T]ATGTATTGAGTGCTT | 5607 |
rs77628442 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565974 | GGAGAACCATTTGGA[C/T]GTAACCTTACAGTAG | 5607 |
rs77642194 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743613 | AGGCAATGTATATAA[A/G]GCTTATCATGGAGCA | 5607 |
rs77643694 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671604 | TAATAAGGAATTATA[A/G]TAAGGACATGTAAAG | 5607 |
rs77664896 | in-del | -/CAGA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787128 | CTGTTCAATGATAGA[-/CAGA]TAGGCAGGCAGGGCG | 5607 |
rs77680102 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595990 | TCTTTTTTTTTTTTT[G/T]TTTTTTAGATTTTAT | 5607 |
rs77680501 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739896 | GTAAAAAAATGTTCA[C/G]TGATATGTGGAACCA | 5607 |
rs77776478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564937 | GTTAGTGGGTGTGGT[C/T]ACAGTGATAATGATG | 5607 |
rs77782036 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740597 | GACCCTGTCTCAACA[A/C]AAAAAAAAGTGTTTC | 5607 |
rs77797361 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705873 | AGAGTACACTCTCAG[C/T]GTATTTAAGGAAGAG | 5607 |
rs77897712 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577412 | GCAGAGCTTTGTGTT[A/C]GGGCTAATAAATGCC | 5607 |
rs77947038 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555054 | GGGAGTTAGGGCTGG[A/T]TGAGGAGAGGGACAT | 5607 |
rs77955129 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565725 | CTGAGATTACTTGGG[C/T]CCACTTTTTTTTATC | 5607 |
rs77962705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789956 | TCTGTGGTCCAGGCC[C/T]GAGTGTCCTTTGGGC | 5607 |
rs78003823 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761094 | AGTGTAAGTTCCTTC[C/T]TTCCTCCTGGAAATG | 5607 |
rs78006582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622231 | AAGTCAAAGAAACAA[C/T]ATAGGACCTGAAGGA | 5607 |
rs78007682 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747843 | TAATTTCAATTTTAA[A/G]TAAATCGGTTTTTAA | 5607 |
rs78017689 | snp | C/G | 0.0487127 | 0.148458 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551745 | TCCTGGCTCAGGCTT[C/G]TGGGATTATTTTCAA | 5607 |
rs78037005 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640032 | TGTTATCACCAACTG[C/T]CTTGTATTTTGCTGT | 5607 |
rs78038536 | snp | A/G | 0.444444 | 0.157135 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638323 | GGAACTGAAAACCAA[A/G]TAACGCATGTTCTCA | 5607 |
rs78042031 | snp | C/T | 0.238749 | 0.249747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604732 | AAACCCCGACTCTAC[C/T]AAAAATATAAAAATT | 5607 |
rs78043334 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646764 | CACAATCTGTCTTTA[C/T]TTGCAAAACAGATGT | 5607 |
rs78057041 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654282 | ATCATTAGAAAATGT[A/C/G]TTTGTCTCTAGTAAC | 5607 |
rs78077978 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606284 | CAAGCCAAGACTCAT[A/G]TTTTCAGCTTTGGGG | 5607 |
rs78100743 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572717 | TATTATTTTTTTTTT[G/T]GAGATGGAGTCTTGC | 5607 |
rs78131470 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723361 | GAAGAGCATTTTATA[A/G]ATTGTGGTTGGCCAA | 5607 |
rs78161566 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773399 | AATAACGTTAGGATC[A/G]AGCATTAGTAAATAA | 5607 |
rs78193483 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740596 | AGACCCTGTCTCAAC[A/C]AAAAAAAAAGTGTTT | 5607 |
rs78227393 | snp | A/C/T | 0.000132176 | 0.00812854 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543510 | ATGCCAGCAAGGGGG[A/C/T]CTCAGGGACTTGAGT | 5607 |
rs78252795 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698899 | AAGCACATTACGGGA[G/T]TCATTTAATCTTCAC | 5607 |
rs78253476 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789141 | CTGCACCTTGCTTTT[A/T]TACTTAGTGAGTCAT | 5607 |
rs78258911 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631000 | TTAGCTTGAGTCACA[A/G]ATATTGTCAAAGAGG | 5607 |
rs78368280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688614 | AATATACAACTTTTT[C/G]TAGCTTGGTTGATTA | 5607 |
rs78432241 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610224 | TGATGTATCATCTCT[A/G]GGTGTTAATTTTAGA | 5607 |
rs78437805 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604883 | CTGGCAACAGAACAA[A/G]AAAAAAAAATTAATA | 5607 |
rs78452110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679313 | GATACAGTTTCCTGC[A/G]TGAGGCAGTTATGGG | 5607 |
rs78455219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553123 | TACTAGATGACTTGC[C/T]TAAGTTGTTAGTAAT | 5607 |
rs78476641 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705034 | TTGATCTCTAAGCCC[C/T]TTTCCAGACTAACAT | 5607 |
rs78510739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642426 | TTTTAGGAGATGAGG[A/G]ATGCATGCTCAAGGC | 5607 |
rs78551590 | in-del | -/CT | 0.498774 | 0.02473 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683752 | GTGACATGAGCAAGA[-/CT]CTGTCTCAAAAACAA | 5607 |
rs78585183 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729392 | GTAAAAATTCCAAAG[G/T]TTGAGAATGTAGCAA | 5607 |
rs78613703 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775944 | TGGGCAATCTCTTAA[A/G]ACATTCCACTTCTAT | 5607 |
rs78627542 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716272 | CTTGAGCCCAGGAGT[C/T]TGAGGCTGCAGTAAG | 5607 |
rs78697483 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804603 | GGAGGAACGCCTCTA[C/T]GCTCCCTCCTGCAGT | 5607 |
rs78713257 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696602 | GTAGATAAGACTTGG[C/G]TGAAACAGGGAACAC | 5607 |
rs78736545 | in-del | -/CGCGCCG | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542550 | ACGCGCCGCGCGCCG[-/CGCGCCG]GTTCCTCGGCTTCCC | 5607 |
rs78753936 | in-del | -/TTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696142 | CTTTTTTTTTTTTTT[-/TTTT]AACCACAACTAGTTC | 5607 |
rs78792407 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551696 | CCCAAGCTGGAGTGC[A/G]GTAGTGAGATCACAG | 5607 |
rs78836369 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560128 | AGTAATTTGCTTAGT[A/C]TGTATTTCTGCTTTC | 5607 |
rs78838508 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761915 | ATAATTTAGGTACTG[G/T]ATCAAACATGTATAG | 5607 |
rs78870035 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596413 | AGCAAGACTCTGTCT[A/C]AAAAAAAACTCAACA | 5607 |
rs78904626 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726136 | TACACATATCAGTGT[A/T]TATTTTGTGTACAAG | 5607 |
rs78914776 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555008 | AGCTGTATTCTTTCT[C/G]ATTTCTTTTTCTGGG | 5607 |
rs78915816 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587319 | GGTAGACAGGACTTA[C/T]CATGCGGGGCCTCGT | 5607 |
rs78925856 | snp | G/T | | | splice-donor-variant | MAP2K5 | GRCh38.p7 | 15:67693570 | ATGCTTATATGGCGG[G/T]AAGTAAACTTATGCA | 5607 |
rs78945981 | snp | C/T | 0.0052248 | 0.0508439 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592912 | TGCCACTAAAAATTA[C/T]CTTTCCTTTTCAGCT | 5607 |
rs78972675 | snp | G/T | 0.226188 | 0.248863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636205 | ATCATGAGGTCAGGA[G/T]ATCGAGACCATCCTA | 5607 |
rs78977390 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804739 | GGGAGGGGCCCGTCA[C/G]TCGTGAGCACAGCTT | 5607 |
rs78985353 | snp | A/G | 0.00278422 | 0.0372069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549230 | TTCTATGCTTATTCA[A/G]TTAAGCTGTCTCAGT | 5607 |
rs79075053 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795075 | CTGCTGTTGTGAGTC[A/G]TCACTCTCAGCATTT | 5607 |
rs79088618 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720410 | TGTAAGTGAAATAGC[A/G]TATGGGAGAGGAAGG | 5607 |
rs79107468 | in-del | -/CTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772444 | TAATTTAAATTCATT[-/CTTT]ATTTGTGTTGCAAAA | 5607 |
rs79107834 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713217 | TTAGTAATAGAAATT[C/T]TCCCAAGGAAAATTT | 5607 |
rs79137260 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731368 | CAACATAAAGGTTAA[A/G]GGGCTGGGTTTTTGT | 5607 |
rs79153127 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577244 | CCGGCCAGTAACCCT[A/G]TATATTAGGGTAAAT | 5607 |
rs79218062 | snp | G/T | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718373 | AAACTTTTTAAAAGG[G/T]TGTTATTTCTTAATT | 5607 |
rs79225149 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685287 | ATGCAAGCCAGAAGA[A/T]AATGGAAAGACGTCT | 5607 |
rs79230595 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621799 | AGTGAACAAAAAAAA[C/T]GAAAGTGTGTGTTTT | 5607 |
rs79237245 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753714 | TAACAATTGGTGACA[A/C]GAATGTGGGGAAATT | 5607 |
rs79243144 | snp | A/G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634765 | AGTGTTAGCATGATA[A/G/T]TTTTTTTTTTACTTT | 5607 |
rs79245035 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663185 | TATCTTACATAATCA[C/G]TGATTAAAATCAGGA | 5607 |
rs79273166 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637473 | TGCCTTGCAAATTGC[A/G]AGGTTTTTCCACACT | 5607 |
rs79309519 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732672 | ATTTCATTTTTTTTT[C/T]CAAAAATTCCGACTC | 5607 |
rs79340934 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711679 | CGTGCACGCACACAC[A/G]CACACACACACACAA | 5607 |
rs79348006 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558049 | GAAATATTACTGATG[C/G]AAAAAGTCCAAATCC | 5607 |
rs79378448 | in-del | -/C | 0.164873 | 0.23506 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786486 | AGAATATAAGAAAGA[-/C]CTATGTCTCAGGAGC | 5607 |
rs79402571 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645733 | ATTTTTTTTTTTTTT[G/T]GTAGAGATGGGTTCT | 5607 |
rs79403995 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600221 | ATTATTTAGTTTGTT[A/T]AATGTTAATTATGGG | 5607 |
rs79463986 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548926 | TTGAAAAAAAAAAAA[A/G]GCACTATAGAGGCAA | 5607 |
rs79465101 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651414 | TAGTTATTTTGAAAT[A/G]TACAATAAATTATTA | 5607 |
rs79477628 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773403 | ACGTTAGGATCGAGC[A/C]TTAGTAAATAATAAT | 5607 |
rs79481569 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692908 | AATAAAAATTAATAT[G/T]GGGAGCAACAATGGT | 5607 |
rs79494958 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721812 | TAAAGTATTTCTTCA[G/T]CACTTTTAATGATGG | 5607 |
rs79525259 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692713 | TTTTAATCTCTGAGC[A/G]AGTTTCCTTCATCAG | 5607 |
rs79532433 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611614 | GAATGTAGCTGAGCA[C/T]ACTAGGTATCGTCAT | 5607 |
rs79545497 | snp | A/G | 0.000131774 | 0.00811601 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586856 | TATAGGTGAATACTC[A/G]GGCCGGACCCTCTCA | 5607 |
rs79547317 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763596 | AAGATTAGCTTCTAT[A/G]GAGATCCTTGGAGGT | 5607 |
rs79552720 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722368 | TTTTTTTTTTTTTTG[G/T]TCCTGCATTACTAAA | 5607 |
rs79585489 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802896 | GGGGAGGGACCAGCC[A/G]CAGGGGCTGGAGACT | 5607 |
rs79622428 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789715 | AGCAAAACTCTGTTT[A/C]AAAAAAAAAAAAGGA | 5607 |
rs79642182 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637159 | CTTTTGAGGTTTTCA[A/G]ACTTGGACTGGCTTC | 5607 |
rs79648152 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549562 | AGTTTATGTTTATTA[G/T]ATTAATTTTTAAGCT | 5607 |
rs79650251 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664932 | TGTCTTACTTAACTA[C/T]TGTTAATGCAAAACC | 5607 |
rs79694093 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797160 | TAGAGTTTCTGATCA[C/T]TCCCTTCTTACATGT | 5607 |
rs79731767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773746 | CAAGTTAAAGATCAC[C/T]CCTAAAAACCTCTGC | 5607 |
rs79780161 | in-del | -/CTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696127 | GAGAAAAGAGCTGAG[-/CTTT]TTTTTTTTTTTTTTT | 5607 |
rs79790429 | snp | C/T | 0.310878 | 0.242475 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552559 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5607 |
rs79803943 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554077 | CATTTTTGGTTTTTT[G/T]GAAATGGTCTGGCTC | 5607 |
rs79812237 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704909 | GATAAGAATCCTAGA[C/T]TGGGAATGGAAGACC | 5607 |
rs79815780 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800321 | AGTGGGGTTTTTTTT[A/T]AGCATGAATGTATTA | 5607 |
rs79860802 | snp | C/G | 0.237303 | 0.249677 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564880 | ACATGCAAAAGATAT[C/G]TACTTTTGGGTATGA | 5607 |
rs79897993 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655532 | TCTTTCATGTTCAAA[-/AT]TRTCATTCCCCTGCC | 5607 |
rs79898373 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597602 | CACTTTCTTATATAA[C/T]GAACACTCTTCCTAT | 5607 |
rs79899657 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752738 | GTGTTCATGAAGTGG[A/G]AGGCTTAATATTGTT | 5607 |
rs79906544 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620648 | AGACAACGATAGTAA[C/T]AATTCAAAATGAAGT | 5607 |
rs79923336 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638239 | ACACACACTGGGCTT[A/T]TCAGAAGGTGGAGGG | 5607 |
rs79934662 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736906 | ATTTCAGCATGTGAA[G/T]AGATCTTACAATGAT | 5607 |
rs79940505 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598206 | TGAGACTTCATCTCC[A/C]AAAAAAAAAAACTAA | 5607 |
rs79964636 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740605 | CTCAACAAAAAAAAA[A/G]GTGTTTCCTTTTCAG | 5607 |
rs79966387 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609590 | CTATAGGTCTGTAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs79978711 | snp | C/G | 0.264084 | 0.249603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756515 | CCCCACACACAGTTA[C/G]TGTGTGTGTGTGTGT | 5607 |
rs79985409 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637017 | TCTTCCATGCTGGAT[A/G]CTTCCTGACCTTGAA | 5607 |
rs80024617 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634764 | AAGTGTTAGCATGAT[A/T]TTTTTTTTTTTACTT | 5607 |
rs80029644 | snp | A/C | 0.0267878 | 0.112589 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680271 | GGACGATTATGAATA[A/C]TACTACTTTTCATAC | 5607 |
rs80056478 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649900 | CCAGCTGGGATTTTG[A/G]TAAGAATTGAATTGA | 5607 |
rs80069524 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714752 | AGTACTCCCAAATTC[A/G]AAATTTTTTGAGCAC | 5607 |
rs80070606 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716540 | TGGTAAAAACCACTG[C/T]TCCTAGAAAATTCTC | 5607 |
rs80075206 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648591 | TCTTTTTTTTTTTTT[A/G]AAACAGAGTCTCGCT | 5607 |
rs80108391 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656763 | GTCAAGTAAAGTTGC[A/T]GGACTGATCTTTAAT | 5607 |
rs80132930 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676238 | AGAGAGAGCACCTGT[A/C]TGATGAATGACAGGG | 5607 |
rs80168967 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800622 | TCATATGAATCGTTT[A/G]TGGTAAATATATTGG | 5607 |
rs80170147 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598204 | AGTGAGACTTCATCT[A/C]CAAAAAAAAAAAACT | 5607 |
rs80200213 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700456 | TGAGAGAGTAACCTC[A/C]GTTTTAGCTTTTTAA | 5607 |
rs80224115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569834 | CCCAGTTCAGTTCCA[C/T]CTCTGTGGAGGGTTC | 5607 |
rs80252004 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664727 | TTTTTAAAGTAAGTG[A/T]TCTGACATTTAAGCC | 5607 |
rs80257409 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600253 | GTCATCTGAGGAGTT[A/T]TCTAGGGCTGATTTA | 5607 |
rs80270090 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790067 | AACTACAAGAGAGTC[A/G]TTTTCTTTTCCCTTT | 5607 |
rs80347963 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639351 | AGAAGCTACCATTTA[C/T]TGATGATTTATACAA | 5607 |
rs80355944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557268 | ATGACTGTTGGATTG[C/G]TGTTCGTGGACAGTA | 5607 |
rs111237366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728971 | TTCTTTTGCTTTCAT[A/G]GTTAAAGCCATCAGA | 5607 |
rs111240932 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708926 | GTATCCCTCTGTTGG[C/T]GGGGTAAAGGACATC | 5607 |
rs111270466 | in-del | -/TA | 0.5 | 0 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703425 | TACGTTGTTTGCACA[-/TA]GACGCTTCTGTGCAT | 5607 |
rs111272531 | in-del | -/TTAT/TTATTTAT | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583744 | AAAATGATTGTTTCC[-/TTAT/TTATTTAT]CTTATTTATTTATTT | 5607 |
rs111312609 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733630 | CATTTATTCTGCCAG[C/G]TTTTGCCACCAGTGT | 5607 |
rs111349530 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601899 | GTGAGTCCTTTCTCC[C/T]GAATATAGTCCTTTA | 5607 |
rs111349686 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585760 | CCCACTTTGGGTCTT[A/G]GGAGCCACTTTTCAA | 5607 |
rs111356803 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594939 | GAGGTACTGTGCACA[A/G]TTGTAGGCATCAATA | 5607 |
rs111383052 | snp | C/G/T | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752450 | TTTGGGAGGCCAAAG[C/G/T]GGGTGGATCACAAGG | 5607 |
rs111405646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699319 | CAGCCAAGCTTCAGG[A/G]CCCACCTAAGTCAGA | 5607 |
rs111438311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551475 | GTAACTGGGACTACA[C/T]GCATGCACCACTATG | 5607 |
rs111443247 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592725 | TTATTGCTTTTGATT[A/G]CTAACAGGGTTTTAG | 5607 |
rs111468310 | in-del | -/TG/TGTG | 0.38934 | 0.207568 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637910 | CTGGAAGCCTGTTGA[-/TG/TGTG]TGTGTGTGTGAGTGT | 5607 |
rs111476365 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758447 | GATCACCAAGCACCT[C/T]ATTCAAAACTATATT | 5607 |
rs111487871 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769855 | ATTTACACAAAGGGT[A/C]ATAAGCATACTTCAG | 5607 |
rs111520298 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611422 | CTGGGGTAACTGACC[A/G]AAGGGGCAAATGAGA | 5607 |
rs111539576 | in-del | -/AGAC | 0.182614 | 0.240747 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787125 | TGGCTGTTCAATGAT[-/AGAC]AGATAGGCAGGCAGG | 5607 |
rs111582492 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657967 | AATAAGAATTTTTAG[C/T]CTCTGATAGGAAAAA | 5607 |
rs111592049 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684817 | TGAAATAAAAATTTC[A/G]TTGATGGAATTAACT | 5607 |
rs111595074 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678034 | TCATTAGAATAACTT[C/T]TATATTGCAATGTGG | 5607 |
rs111595810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804734 | GTGGGGGGAGGGGCC[C/T]GTCACTCGTGAGCAC | 5607 |
rs111610342 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599662 | TTCTGCCCATGCAAG[A/G]CAGTGCAATTCCCTG | 5607 |
rs111614943 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644286 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 5607 |
rs111631060 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802544 | TTGTTGCAATTGGCC[C/T]TCAGAGAATCCAGGG | 5607 |
rs111636172 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741957 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 5607 |
rs111659713 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624638 | GTGTGTGTGTGTGTG[A/T]GAGTGTGTTTGACGG | 5607 |
rs111678501 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567309 | CCACTTCTGGGATCA[C/T]GGCTTTTCCTCTGAC | 5607 |
rs111681537 | in-del | -/A | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607287 | TATTAATGTTTTCAG[-/A]AAAATCAATGAATAT | 5607 |
rs111747464 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714890 | CAATATCTGAAATAT[C/T]TCTGGTCCCAGGTAG | 5607 |
rs111748545 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599971 | GTATAATAGGTTTTA[C/T]AGAACCTTGAAAAAC | 5607 |
rs111760319 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555000 | ACCTGAGGAGCTGTA[C/T]TCTTTCTGATTTCTT | 5607 |
rs111761448 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584291 | AGAAGTCAATTGAGG[A/G]GTGAGGCAGATGTTA | 5607 |
rs111785487 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549343 | GTAGGCTAGATTAAC[G/T]TTATTTCGGTGTCAT | 5607 |
rs111790167 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553775 | AAAATTAGCCGGGCG[C/T]GGTGGCGGGCGCCTG | 5607 |
rs111803674 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563631 | TTCCTGTATTTTTTA[C/T]GCAGTACTTAAAGTA | 5607 |
rs111833543 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601361 | ATAGTTCTCCGACAG[C/G]GAGGTCTTCTCATGC | 5607 |
rs111835930 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585689 | GAGGTGGTGTCAGAA[A/G]GCTCTTTGCATTTAT | 5607 |
rs111842023 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580422 | AAAATCCAGGGAAAA[A/G]GAGCAAGAGGCAATT | 5607 |
rs111864951 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776640 | TGAGAGCATTAAGAT[A/G]GGGGTTCAGGTTGGT | 5607 |
rs111871659 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545522 | CTTGTACCTTCCTCA[A/G]AGACTTGGAAAGATT | 5607 |
rs111897951 | snp | A/G | 0.232943 | 0.249417 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799046 | TGGTGGCGGACACCT[A/G]TAATCCCAGCTACTC | 5607 |
rs111902953 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630948 | TACTGGATACATTTT[A/G]TGAAATTCTTGATGT | 5607 |
rs111904051 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652866 | CTCTAGGTACCTCAT[A/G]TAATTGGAATCACAC | 5607 |
rs111904926 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547386 | TATTTGTCTGATTTA[C/T]TGAAAGGAAGAAGAA | 5607 |
rs111925190 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566706 | AATTACTTTTTCCCC[C/G]TCTTGGATGCAGGCA | 5607 |
rs111962616 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720202 | GCTAGGGTTTTTGGT[G/T]TAATGTAGTATAGAC | 5607 |
rs111963369 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728953 | TGAAATGTCTCTTTC[A/G]TATTCTTTTGCTTTC | 5607 |
rs111970649 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597137 | TCACGTCACTGCACT[C/T]CAGCCTGGGCCACAG | 5607 |
rs111977255 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587113 | GGGGAGAGTGACGTT[C/T]CTGTTTTGACCTGAA | 5607 |
rs111981804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564418 | TAGTCAACAGTTAGG[C/T]TGTAGGTTTTTGATA | 5607 |
rs111989109 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586723 | AGACTCCAACTGTGG[A/G]TTTGTCTAGCAACAA | 5607 |
rs111994243 | in-del | -/GA | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715235 | TTTTTTTTGGGCGGG[-/GA]GGGGGGGGGTCTAAA | 5607 |
rs111999353 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647270 | CTGTCATAAGGTGTA[C/T]AACATGCTCTAAATT | 5607 |
rs112000317 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557251 | GAAGTAACTGCTATA[A/G]AATGACTGTTGGATT | 5607 |
rs112024503 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723006 | GTGCTCTTCAGTAGA[A/G]CTGTAAATTTAAAAC | 5607 |
rs112046190 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705499 | CAACACTTTGGGAGG[A/C]TGAGGTGGGCAGATC | 5607 |
rs112058422 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680819 | GACAGTATTGTGACA[C/G]GAGACACATGTTGTG | 5607 |
rs112060598 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653375 | ACAGCAACCTCTGCC[A/T]CCTGGGTTCAAGCCG | 5607 |
rs112075849 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586142 | GGTACTGTATTTTCA[A/G]TTATTTGGAATTGTT | 5607 |
rs112088622 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732961 | TAGCTCTGTGGGGAG[C/G]GGGGGCTTAACAGCG | 5607 |
rs112096459 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672215 | ATGGTATTTCTAGTT[C/G]TAGATCCCTGAGGAA | 5607 |
rs112135598 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707199 | GGATTACAGGCGTGA[A/G]CCACCATGACCAGCT | 5607 |
rs112149071 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581165 | TGTGGCTCATGATGG[C/T]GGCCAAAGCTGCTAT | 5607 |
rs112154075 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609440 | CTATAGGTCTATAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs112171147 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637229 | ACCTTGTCATCCTGT[G/T]AGTCAATACTCCTTA | 5607 |
rs112195835 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737738 | TTTTGGGAAACCAAG[A/G]CAGCCAATTGGAACC | 5607 |
rs112204342 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709995 | TGGTGAATAATCTGA[C/T]AGACTTTTCTATAGG | 5607 |
rs112220979 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638583 | ATTCATTTGGGTATA[A/T]ACCCAGTAATGGGAT | 5607 |
rs112235244 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648173 | CCACTGTATAATTCC[A/G]AAACACTTTTTACCA | 5607 |
rs112236774 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566980 | GTTAAATAATAACCA[A/T]CATATTAAACCAAAG | 5607 |
rs112319446 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591004 | AAGAAAGACATCTAT[A/G]CTGACAACTAGCATG | 5607 |
rs112322701 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766884 | CTCACCATCCCCCTA[A/C]CACTCAGTCTTCTGC | 5607 |
rs112367013 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705609 | GGTGTGGTGGTGTAC[A/G]CCTGTAATCCCAGCT | 5607 |
rs112378066 | snp | A/G | 0.251578 | 0.249995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694557 | ATCAAAACCACAATG[A/G]GATACCATCTCACAC | 5607 |
rs112405785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593264 | TGGGCTGTTGAAATG[A/G]CCCTGCATTCTGAGG | 5607 |
rs112417288 | in-del | -/TTAAA | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613178 | GAAGCTGGATGATTC[-/TTAAA]TTAAAGTTGTCTTAT | 5607 |
rs112421874 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559856 | TTGGTCAGATGGCAA[A/G]GAACCTCCATGTATA | 5607 |
rs112423380 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800233 | CGGGGATTAGATTGG[C/T]AGCTTTAAAACTTTA | 5607 |
rs112431516 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731992 | ATTTAGCAGAGTAAC[A/G]GGAGATCCAGAGGGA | 5607 |
rs112470760 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643826 | ACGCCTGGCCAATGT[C/G]AGGACTATAAAATGT | 5607 |
rs112478905 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643468 | TTTATTTTTTTTGAG[A/T]CAGAGTCTCGCTCTG | 5607 |
rs112505481 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806860 | TTGCTGGGCCCTGGC[G/T]TCCCTGCCCTCGCCT | 5607 |
rs112507532 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806181 | TTTTATAGGAGAGCT[A/G]TAGACAAAGGAGAAA | 5607 |
rs112522094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787936 | TAAAAATGTTACTGC[A/T]GTCTATTACCCAAAA | 5607 |
rs112528705 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779851 | GCTGCTCTTCAGTGC[C/G]GTGCCAGATTTGCGG | 5607 |
rs112550275 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683066 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 5607 |
rs112561988 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636150 | GGGCGCCGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5607 |
rs112614374 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707007 | TGCAACCTCCGCCTC[C/G]CAGGTTCAAGTGATT | 5607 |
rs112615637 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728340 | AAAGCATCTAATCTA[A/G]GTCATTATTTTTGCT | 5607 |
rs112662502 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619763 | GAGAACCTTGTTCTA[A/C]AAAAAATAAAAATAA | 5607 |
rs112663435 | in-del | -/TTTTCAACATGAGA | 0.319616 | 0.240112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555444 | AACATTGGGGATCAC[-/TTTTCAACATGAGA]TTTGGAGGGGACAAA | 5607 |
rs112678113 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549483 | ATGATGAGTGCGAGG[C/T]ACAGTGTTGCTTGTT | 5607 |
rs112686860 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773056 | TTTAGAATTCAGAGG[A/T]TTGGTAACAGAAGAT | 5607 |
rs112687929 | in-del | -/T | 0.0356815 | 0.128715 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713137 | ATAGAAAAAAAATCA[-/T]TTTTTTTTCCCCAAA | 5607 |
rs112700436 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728313 | TGAGTTAAAAGATTA[A/G]GACAAAGGGTGAAAG | 5607 |
rs112712383 | snp | A/G | 0.000814759 | 0.0201672 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693605 | TAATGTTTAAAACCA[A/G]CATCTTTATCTTTAT | 5607 |
rs112722775 | snp | A/T | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680489 | CATACTTTGTTAAAG[A/T]GTGACCACATAGTGA | 5607 |
rs112725698 | snp | A/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704825 | CTTTTGCATATTTTA[A/T]ATTGTTATCATTTAT | 5607 |
rs112728118 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575847 | AGTGAGGGTTAGTTC[C/T]CTCCCTCTATCTCTA | 5607 |
rs112750709 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735493 | ACTCTGTGCCTGACT[A/G]AGCACTAGGAGCACA | 5607 |
rs112766168 | snp | G/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736286 | TTAAGGTCTCTGCCC[G/T]TGAGGACAGTTGGCA | 5607 |
rs112771096 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719918 | AGTGCACAGAATACC[A/C]TGGAAAAAGACCTTT | 5607 |
rs112773064 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548799 | TTCCTCAAAAAGTTG[A/T]TGTTTCATTTGTGAG | 5607 |
rs112777964 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744061 | GAGCCTCAGCTTCCC[C/T]AAAGCAAAGTGAGTA | 5607 |
rs112801761 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641204 | ACAGGAAATTTCTTA[A/G]CATTGTATATTGCAT | 5607 |
rs112827894 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584926 | TGGTCTTGATCTCTT[C/G]ACCTCATGATCAGCC | 5607 |
rs112873684 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755132 | GGTGTGCACCACCAC[A/G]CCCAGCTAATTTTTT | 5607 |
rs112907014 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637090 | CACCAGTGATTTGCC[A/G]GGGGCTTTCAGGCCT | 5607 |
rs112909477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806473 | CAGTATGTCACTGCT[C/T]GTCCCTGGGCCTCAA | 5607 |
rs112912627 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786639 | CTCGGGCCTGAGTAC[A/C/G]GAACTTGGAAAGTGG | 5607 |
rs112915409 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782484 | AAATATTTCATACAG[C/G]CTGATTTTAGTTAAT | 5607 |
rs112957580 | snp | A/C | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669793 | CTGAAAAGAGATAAC[A/C]ACAAAAAACCTGATA | 5607 |
rs112967216 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543749 | ACACAACCACGCAAA[C/T]GCAAACTGCTGAATC | 5607 |
rs113000230 | snp | C/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632457 | ACATAGTAAGCCTGT[C/G]TACTTTAGATTAGGA | 5607 |
rs113007427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720098 | TTTTTCCCCTTTTTT[A/G]TTTATCAATTAGCTG | 5607 |
rs113022716 | snp | C/G/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554750 | TTCCACTCTTTCTCT[C/G/T]TTCTTAGTAATGAGC | 5607 |
rs113103371 | snp | C/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729695 | CTTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 5607 |
rs113149031 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629687 | CCCTATGCCATTCCT[A/G]TCCTAACACTTACCA | 5607 |
rs113151229 | snp | A/G | 0.0244538 | 0.107838 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541729 | CAGTTACTCGGCAGG[A/G]GTTGGGGGCTGGTGG | 5607 |
rs113166660 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744048 | GCTGCTCCCCTCTGA[A/G]CCTCAGCTTCCCTAA | 5607 |
rs113176448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805477 | GAGGCCATGCGGCTC[C/T]TTAAGCAGCCTCTCT | 5607 |
rs113281158 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543762 | AATGCAAACTGCTGA[A/T]TCTAGAAGAGAGGTT | 5607 |
rs113286421 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670833 | AACAGAAACTTAGAA[A/G]TTGCTGTTATCATTG | 5607 |
rs113289328 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621921 | GGGTGCGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 5607 |
rs113293372 | in-del | -/TTG | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687388 | AAAGAAACATCCCTA[-/TTG]TTCAGAAAGAAACCC | 5607 |
rs113333627 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705351 | GGAGTTCCATTTGGC[A/G]AGGGCTGGGGCATGA | 5607 |
rs113357246 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763361 | CTGCTATGTAGTTAT[A/G]GCTACTCACACTCTA | 5607 |
rs113426585 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615294 | TGAGCCACTGTGCCC[C/G]GCCTGTTTCTTAACC | 5607 |
rs113440700 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721143 | TTTGTTCGTTTTTTG[-/T]TTTTTTTTAAGTTCC | 5607 |
rs113453175 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621770 | ATGTAGTTTTAGGCA[A/C]TGGAAATAATAGCAG | 5607 |
rs113454344 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600593 | CTTGAAATGACCCAG[A/G]CTGCTTGTTGTTTAT | 5607 |
rs113471307 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713838 | GTCATTTTCTTTCCA[A/G]TATCATTTTTAGATT | 5607 |
rs113480888 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729720 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 5607 |
rs113486801 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796596 | CAGGCCCCATCCCCA[A/G]CATTGGTGATTACAT | 5607 |
rs113520060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742731 | TCATTTTAAATTACA[A/G]TTCTAAGCCCCTGCT | 5607 |
rs113547193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768828 | GCGCTCTCTGTCATT[A/C]TTGGAAAAACTCCTA | 5607 |
rs113550303 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806964 | TTCTGGTTTGAAGGC[A/G]CTGACACTGGCAGAG | 5607 |
rs113552271 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546509 | CCTGGGCAAGTCAGT[C/T]GGTCTCTCTGGGCCT | 5607 |
rs113557186 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696600 | ATGTAGATAAGACTT[A/G]GGTGAAACAGGGAAC | 5607 |
rs113560683 | snp | C/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654207 | ATATATTTTGGCACT[C/G]CGTTGTTAGGTCCAT | 5607 |
rs113560830 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678603 | GGGAATCCTCAATTG[G/T]TATGGTTTTTCTTTT | 5607 |
rs113589707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598714 | ATGCCATACCTACCC[C/T]TTTGCCTATGAAGTG | 5607 |
rs113594951 | in-del | -/TGTGTGTG | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774168 | AGTGATGTGTGTGTA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs113611682 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713059 | AAGAAAAATTTTAAA[C/T]TTTAATGTTATAACA | 5607 |
rs113647681 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631286 | GTGAATTGCTGTATC[C/T]CGTTAGAATTTTTCC | 5607 |
rs113743393 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761065 | CATTCCAGAATGGAG[A/G]CAGCATTCCAGGGAG | 5607 |
rs113756137 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713061 | GAAAAATTTTAAATT[A/T]TAATGTTATAACATG | 5607 |
rs113772188 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719431 | AACCTACTGCAAAAT[A/G]CTATTTCTGATGTCA | 5607 |
rs113773073 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732904 | GCACCTGAGATTCGG[A/G]TGATTAGTGTGTTTT | 5607 |
rs113777073 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729802 | TACTGCCACATTTGA[C/G]AAGTGAAGCACATGA | 5607 |
rs113783624 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627731 | TGTACCCTTAAAACA[A/G]GTGAATGTTATCATA | 5607 |
rs113785879 | snp | A/G | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604570 | AATGTCTTATGCCTC[A/G]GTTTTCCCATCTGCA | 5607 |
rs113787488 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587324 | ACAGGACTTATCATG[C/T]GGGGCCTCGTAGGCC | 5607 |
rs113799660 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723276 | TGATCTCTCTTTCAC[A/G]CACAGGCACACATAC | 5607 |
rs113845304 | snp | A/G | 0.226188 | 0.248863 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639130 | AAAATTGACAAATGG[A/G]ATCTAATTAAACTAA | 5607 |
rs113849123 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618780 | AGCTGACCACCTTTC[A/G]TCACTGTTTTCTTGC | 5607 |
rs113899908 | in-del | -/T | 0.0352966 | 0.128072 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728201 | TGACATTCGGGATTG[-/T]TTTTTTTCCTGGTCC | 5607 |
rs113950527 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609495 | CTATTCTATAGGTCT[A/G]TAGATTCTGTAGACC | 5607 |
rs113967425 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802104 | CCCCTGCCTCCACGT[G/T]GGAGGGGCCCGGGAG | 5607 |
rs114079025 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802930 | AGGAGCCTCGAGGTT[A/G]GCTGTCTGATTGCAG | 5607 |
rs114105873 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614495 | TTCTATTTTCCCCCA[C/T]ATATATTGCCTAACA | 5607 |
rs114114619 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741456 | CCTGGAGCAACCCAC[G/T]TCCTGTCTGAGAGGG | 5607 |
rs114123910 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589256 | AGGATACAATTTTTT[C/G]TTTTTTTTTTCTTTT | 5607 |
rs114150257 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630181 | TGAGGCTGCAGTGAT[A/C]TGTGATTATGCCACT | 5607 |
rs114162317 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713998 | GTCAGTTTCTTATGT[A/G]TAAGTTGAAGGTAAC | 5607 |
rs114167883 | snp | C/T | 0.00353182 | 0.041874 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592902 | TTGATGATCTTGCCA[C/T]TAAAAATTATCTTTC | 5607 |
rs114175666 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580908 | AAAGGTTTAAATGCA[A/C]ATAACATGATGTTTA | 5607 |
rs114176871 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550361 | ATTGTGATAATATTG[C/T]AGGACAAAATGAAAC | 5607 |
rs114188928 | snp | A/G | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740542 | AGGCTGCAGTGAGCT[A/G]TGATTGCACCACTGC | 5607 |
rs114192272 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734506 | TAAAAACATTGAGCA[C/T]TTTTCAAATGCTAAT | 5607 |
rs114194155 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632885 | TACAGCACCTAGAAT[A/G]TGTTACGTGGCATTA | 5607 |
rs114278097 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639389 | CATTTTGCATGCATT[G/T]TTTAAATTAATGCTC | 5607 |
rs114284681 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559645 | ATTTTTTCCTCCATT[G/T]TAAGTGACATTAACA | 5607 |
rs114318942 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559070 | CCACGTCATTAACTC[C/T]GTGCCTGAGAAGGGC | 5607 |
rs114402736 | snp | G/T | 0.238171 | 0.24972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602784 | TCAGCCTCCCAAGCA[G/T]TTGGGATTACAGGCG | 5607 |
rs114407280 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630227 | TGTCAGAGAGAGCCC[C/T]TGTCTGAATCAGTCA | 5607 |
rs114433191 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750003 | TTCCTCACCAATACT[A/G]TGTGTGTTTCTCATT | 5607 |
rs114455172 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783382 | AAACTTCTGGCAGTC[C/T]CCAGATGCGTGAGGC | 5607 |
rs114556752 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774433 | AGGCACCACTGCTTT[G/T]GCAGGGCTCAGTGAG | 5607 |
rs114641379 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654873 | CAAGATTAGCCTGGC[C/T]GAGTTGGTGAAACCT | 5607 |
rs114648127 | snp | G/T | 0.000745573 | 0.0192933 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670413 | CATGGTTATATGTGT[G/T]TTTTAGCAAACAAAG | 5607 |
rs114651777 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766292 | TTCGTTCTTTACCTC[C/T]GTGCTTAGAAGTTCA | 5607 |
rs114653911 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741582 | TTGCTGACTAATGTA[G/T]GTCTGAACCACCTAC | 5607 |
rs114764316 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794172 | GGAAAATGCAGGTCA[C/T]ACCAGTCACCACCAT | 5607 |
rs114774998 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592152 | GACTTTCACTAAATT[C/T]ATCCATATGAGTGTT | 5607 |
rs114800364 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802562 | AGAGAATCCAGGGAA[A/T]GAGAGTGGCTCTCAC | 5607 |
rs114803407 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784674 | TAGTTGGTTATCTGA[A/G]GGGAAGCTGTGAGAA | 5607 |
rs114806907 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584172 | AATATTAATAAGTGT[A/G]AACATTGACTAGCTT | 5607 |
rs114834730 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747327 | TTATCTCAGAAAACA[A/G]TTGACCCATCAGTAT | 5607 |
rs114856498 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778683 | AGCAGAAGGGTAGGG[A/G]GATTTCTTACCTGTT | 5607 |
rs114880184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587576 | GCACTTTATCAGCCA[A/G]CGCAGCTCCTTCCCT | 5607 |
rs114880931 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556262 | GTTTGTTCTGGTCTT[C/G]TTATTCTCTCTTCTT | 5607 |
rs114882256 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664878 | TGTCAAACTTGTAAA[A/G]AGATATTTCATAGTA | 5607 |
rs114901177 | snp | C/T | 0.0599851 | 0.162463 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542519 | AGACCAGTCTCTCCC[C/T]GACTCGCCACGCGCC | 5607 |
rs114922417 | snp | G/T | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547011 | TCGAGGCTATAGGGA[G/T]CTGTGATTGCACCAC | 5607 |
rs114956229 | snp | A/G | 0.031825 | 0.122064 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582466 | CTGAAAATTTCCATT[A/G]ATTTCTCTATTGACA | 5607 |
rs114974415 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674681 | TCAAGAGATCAGAAA[C/T]GCTACATGTCTTAAA | 5607 |
rs114991920 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753205 | AACTCAAAAAATGGA[A/T]CAAAGACTTAAATGT | 5607 |
rs115011770 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786859 | TCAATAAATGGTAAC[C/T]ATTTTTATCGTCATT | 5607 |
rs115031344 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637720 | CTTCCTTGGCCTCCT[C/G]AGACTCTCAGTTTTG | 5607 |
rs115032678 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636748 | GTGGTGGGTAATATT[A/G]AGTGTTAACTCGATT | 5607 |
rs115042879 | snp | C/T | 0.031825 | 0.122064 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594642 | GATATCTTAGTGGCT[C/T]CAGTTATGAGGTTCT | 5607 |
rs115071048 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660365 | CCAGATTGGCCCATG[G/T]CTAATACCTGGCACC | 5607 |
rs115092472 | snp | A/C/T | 0.0684329 | 0.174426 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777300 | GCACCCACACAGTTA[A/C/T]AATTTGGGCTCAGAG | 5607 |
rs115154372 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589257 | GGATACAATTTTTTC[G/T]TTTTTTTTTCTTTTT | 5607 |
rs115168463 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787159 | GACAACAGGACTGAT[G/T]CCGCCTGCCCCTGGT | 5607 |
rs115185608 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750312 | GAAACTTGGGAAATG[A/G]ACATTGCCTTTGCTA | 5607 |
rs115221094 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638080 | TTAATTTAACTTTTT[A/T]AATTTAACTTTTAAG | 5607 |
rs115246887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620121 | TAACGCCTGTAATCC[C/T]GCACTTTGGGAGGTT | 5607 |
rs115250528 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721667 | TTAATTAAGCTGCTG[G/T]TGCCTCCATTGGGCC | 5607 |
rs115271485 | snp | A/C/T | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574120 | GGGTATGGATAAGGA[A/C/T]CCCTTTCTGATAACA | 5607 |
rs115306287 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718007 | CCATCACTGGAAGCA[C/T]GGCACATTTCAGAAA | 5607 |
rs115335635 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778330 | GTGGTCCCTTTAAAA[A/T]TCAGGGTAACCATGA | 5607 |
rs115340097 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594161 | GCTAAGGAGAATCTA[A/G]TGTGGTGTATGTATA | 5607 |
rs115347790 | snp | C/T | 0.046775 | 0.145601 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628088 | GCCACGCAAGGTGGA[C/T]GGAAGAGCTGTGGGA | 5607 |
rs115444512 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665770 | AGAGTATAGTTGGTG[C/T]GAAAGGTAGGTGTAG | 5607 |
rs115509350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686516 | GGAGGCTGAAGAGAA[A/T]CACTTGAACCCAGGA | 5607 |
rs115521477 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650381 | GACTGATGAGAGCAG[A/G]CATCCTTCTCTTGTT | 5607 |
rs115607099 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762867 | GGCCTTTCAGTGGCA[A/G]AAATTCAGGCCTTTA | 5607 |
rs115609244 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738318 | CTCCAGGCCTAGTTG[G/T]TAAAATCCTTTAATC | 5607 |
rs115634824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645923 | AAAATAGCCAATGTG[A/G]CTAAAATAGAGTGCA | 5607 |
rs115680368 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608821 | GTTAGAGTGATTAAT[A/G/T]TACTCTTTCTACTCT | 5607 |
rs115688536 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587543 | AAATCTCTTACTGAA[C/T]ATCCCTGTCGGAGGA | 5607 |
rs115722112 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794411 | CTTTTTGTGCATTTC[C/T]TTTTTTAAAAAAGGA | 5607 |
rs115756216 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800748 | GGGCTCAGTGTACCT[A/G]GGCTTTGGTGCACTC | 5607 |
rs115837796 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610744 | GAGGAGCAGTTTGCA[A/G]AATTTGAGGGGGAAT | 5607 |
rs115868303 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572200 | TTTAAAGAATGCCTG[A/G]TGAGTCAGTAGGAGC | 5607 |
rs115876847 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690825 | ATGCGTGAGCCACTG[C/T]TCCCGGCCATGTATT | 5607 |
rs115908648 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657088 | GATAGTTAAGGAAAG[C/T]GGGTCTAACTGAGGT | 5607 |
rs115922306 | snp | A/G | 0.031825 | 0.122064 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570069 | AGTTTCAGCTGAGAG[A/G]ATCCCATAAATTTTG | 5607 |
rs116042465 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553593 | TCTGAACCAGAAATC[C/T]GAACCAATAAATGGA | 5607 |
rs116067154 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717733 | ACTTCATATGCGTGT[A/G]TGATGCTTTGGTGGG | 5607 |
rs116129664 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713449 | AGTATTTAAAAGGTG[A/G]CATGGGCCATGTGTG | 5607 |
rs116167021 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548837 | CTCAGAAAAAAAAAT[C/T]TCTTTTGGCTGTAAT | 5607 |
rs116182090 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555217 | GCATCTGCTTGCATT[C/T]TGCTGAGGAAGCTTT | 5607 |
rs116200200 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637650 | CCCCCTCGGCAGACC[A/T]CTGGAGCTCTCTCCC | 5607 |
rs116259510 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551108 | GAAAAATTTCAGTTT[C/T]TCCACAATAGGATAC | 5607 |
rs116270423 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804437 | GCAGCAGCAGGAGAC[C/G]AGGTCACCTCCCAGC | 5607 |
rs116302598 | snp | A/G | 0.0244538 | 0.107838 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682169 | TATGGCTTCGAGTGA[A/G]GCTGAAAACAAACAA | 5607 |
rs116339282 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772401 | TGCTTTTTTCACATT[C/T]GCTTCAAAAGTAGAA | 5607 |
rs116355127 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754893 | CATGTTGAAATCTGT[A/G]TTTTTTTCTAAGACA | 5607 |
rs116364545 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785026 | CTCAGTGCAGCCTCA[A/G]TCTCCCAGGCTCAGG | 5607 |
rs116389746 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702012 | CCTCAGTTTTTACAT[C/T]TGTAAACTGAGGGCA | 5607 |
rs116422594 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690056 | CTTCAGCTATTGTTA[A/G]TGTATTTTATATGTG | 5607 |
rs116456926 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596469 | AGAAAAAAAAGGGAG[A/G]GGGAATATATATCTA | 5607 |
rs116480629 | snp | A/C/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647485 | GGCACGGTGGTTCAC[A/C/G]CATGTAATCCCAGCA | 5607 |
rs116511719 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737006 | ACCAGGTATTCAGCA[A/G]CAGGGCCAGACTGTC | 5607 |
rs116515581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693246 | ATATCAGGCGGGTTT[A/G]GGATACTAAAGCGAT | 5607 |
rs116569960 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599699 | GATTTTTTTTTTTTT[C/T]AGGGCTTGCAGTGGC | 5607 |
rs116681942 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632223 | TCCTACTTCAGCCCC[A/T]TGAGTGGTTGGACCA | 5607 |
rs116724515 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787187 | GGTGGGCCAGACCCT[C/T]TGGCTGAAGCTGATT | 5607 |
rs116730705 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683717 | GTGAGCCGAGATCGC[A/G]CCATTGCACTTTAGC | 5607 |
rs116739553 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649258 | TTTTATTGTTGAGTT[G/T]TGAGAATTCTTTATG | 5607 |
rs116790337 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652280 | ATTTTAACCTTATTA[A/G]CCATGATATTAGTCC | 5607 |
rs116802915 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620753 | ATTGTTTAGGAGAAG[A/G]ATATAGATAACAATT | 5607 |
rs116804432 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743446 | ATTATTGGAAGTAGT[A/G]TATATTATCCATTTA | 5607 |
rs116811360 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737807 | GATGGTGACCACCAC[A/G]GGGAGAAGGAAAGAA | 5607 |
rs116821207 | snp | A/T | 0.0032039 | 0.0398959 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692438 | ACAAACGCTGTAGAT[A/T]CATGGAATTAGTTAC | 5607 |
rs116826181 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629751 | GTATAAAATCCTCTA[C/T]AGGGCAAGATTTTTA | 5607 |
rs116914237 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564662 | AGAATTTAGAGCTGG[G/T]CTCATCAGTACCTTG | 5607 |
rs116926486 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700307 | CACTACTCTTTACTG[G/T]TCTTATTAAGAACAG | 5607 |
rs116934013 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642053 | TTGGAATCTCCTCTA[C/T]TCTAGACTAAAGCAA | 5607 |
rs116944661 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726468 | AATTTTAAATCCAAG[A/G]TAAGGTGCATACTAA | 5607 |
rs116954844 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549690 | GTCTGACTCTCAAAA[C/T]CCCTCTCTCTTTCAA | 5607 |
rs117011165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711358 | TTTCAGTTTACCAAG[A/G]TATCAGATCCAGATT | 5607 |
rs117049092 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784529 | GGGCCGTGGTCGAGG[C/G]AGAGAGCAGATGGCT | 5607 |
rs117049462 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736484 | TTATATTTCCAGAAA[A/G]TTCTTCAGGGATTTA | 5607 |
rs117050084 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769389 | CCTCTCTCAGCTCTC[A/C]TGTTTCTCACCATTG | 5607 |
rs117053229 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774405 | ATGCATTCCCAGAGG[C/T]ATAGCAGTGGTGAGG | 5607 |
rs117071053 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598823 | CTTAAACCTTAGTGC[C/T]ACAAATGCAGAATTT | 5607 |
rs117102195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725341 | ATGACCACTTGCAAC[C/T]GGAAGCTTTGTGTTG | 5607 |
rs117104217 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608913 | CTCACAGGGCCAGCA[C/T]GGTGCCTTACCTACT | 5607 |
rs117130911 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678000 | ATTTGGATGACCTAC[C/T]CTTTCTTATGTGATG | 5607 |
rs117139633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800803 | ACGTCCTAAGTGGAC[A/G]TCTTTTTTCAAATGA | 5607 |
rs117151147 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754572 | CATTATGTTAAAAAC[C/T]ATAATAAAGCTATGT | 5607 |
rs117174714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699840 | TTAAAACTCACTGTA[C/T]TTGACAGCATATTGG | 5607 |
rs117203809 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605675 | ATTTCTTTTCTTTTT[G/T]CTTGGTGTTCTTCCC | 5607 |
rs117260725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733554 | GAATAATTTGGACTA[C/G]GGTAAAAGGAAGGTC | 5607 |
rs117280989 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559777 | CTCATTGTGAACCAA[G/T]GTATCAGATCTGTCT | 5607 |
rs117314020 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608460 | TGTGTCTGGATAGAT[A/G]AGGAAGTTCTGTTCT | 5607 |
rs117316850 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567893 | TTGTCTGGTAGTTCT[A/G]TGGAGGCCCAGTTCT | 5607 |
rs117329505 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754524 | ATGACTTCATGATCT[A/G]GTGGAAGACAAACTC | 5607 |
rs117345535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564295 | AGAATAGATGTGAAA[A/G]CCCTTTGAAAAGTTA | 5607 |
rs117365064 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662709 | ATACTTAGGGTCATG[A/G]AAACATCTTTTTTTC | 5607 |
rs117394248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640858 | GTACCATGAATTTCT[A/G]TTTTATACTATTGAA | 5607 |
rs117403257 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757618 | ATAAGATGCTCTTTC[C/T]ACCATTAAAGAGCAG | 5607 |
rs117466732 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626506 | CACTCTAGTCTGGGC[A/G]ACAGAGCAAGGCTCC | 5607 |
rs117466843 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706361 | TTGAATTTTCAGGAT[C/G]GAAGAGGATTAGGTA | 5607 |
rs117472509 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573120 | CCCTTAATCATAAAT[A/G]GCTAGAGCCTAGGAA | 5607 |
rs117482388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598548 | TCCCCGCCTGTGCCC[C/T]GACAGTGTTGGATGC | 5607 |
rs117484260 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698757 | TAATTGTCTTTACTC[A/G]GAATAAAACACATAC | 5607 |
rs117500991 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667392 | CCTTCTTAAAAGCAC[A/T]TGTACTCATTTTTGC | 5607 |
rs117530100 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720651 | ATTGCTATGTGGCGG[A/T]TGAGCCCCGTCAGAA | 5607 |
rs117567673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647910 | CTAAGCATGGTGGTA[C/T]GGGCCTGTAGTCTCA | 5607 |
rs117586992 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680285 | AATACTACTTTTCAT[A/G]CACAAGTCTTTATGT | 5607 |
rs117607405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543706 | TGCCCTCAGAGAGCT[C/T]ATGGCCCGGGCTGGG | 5607 |
rs117614006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604054 | GTAATTACAATGTAT[A/G]TGATTTAACAGTTGA | 5607 |
rs117623256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603197 | AACTCTTCGTCTTGT[A/G]TAATCGAAACTCTGC | 5607 |
rs117642045 | snp | G/T | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784944 | GTATCTGAACTGTTT[G/T]TTGTTTTTTCCCTGA | 5607 |
rs117672098 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727308 | GTGACTGGCTCAGAA[A/T]CAGAGCAGTTTACAA | 5607 |
rs117701477 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556400 | TTGAAGAAACATTCA[C/T]TGATATTCTTTTTTC | 5607 |
rs117722043 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786387 | AAAATGTAATGAGCA[C/T]CTTGTTGGAGGGAAT | 5607 |
rs117739826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615926 | TTGTTCAGCCTTATA[A/G]TCTTTTGGGAAAATG | 5607 |
rs117770985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747636 | GTGTGAAACTTCCAT[A/G]AATTTGATTTTCCCA | 5607 |
rs117789680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701475 | GATAAATAATAAGAT[A/G]TGAACAGCATTTTAA | 5607 |
rs117790274 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541948 | GTGCTATTTAGTTGA[A/T]AATACATGGACTAGA | 5607 |
rs117825623 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771352 | CCAGTGCTAATCTTA[C/T]CTCGCTGTGTGGTCT | 5607 |
rs117844001 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657295 | GGTACATGTGGATGG[A/G]TTTTCACCTCCTAGT | 5607 |
rs117846544 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637622 | ATTCATTACTCAGCT[A/G]AAGACTCCAGGACCC | 5607 |
rs117865042 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633623 | GATTTACAAATATAC[C/T]GTTCACTAGACCTGA | 5607 |
rs117873224 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774961 | TGGAAGTTATAGATT[A/C]ACTATTTGGGAACTC | 5607 |
rs117887146 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754735 | GGGAGGGACACCACC[A/G]TAGGTATCTAAGTGT | 5607 |
rs117889772 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757587 | CCCAGAGCTCGGTAC[C/T]GGGGATAGAGAATGA | 5607 |
rs117911928 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633498 | TAGTTGGGTGTGGCA[A/G]GGGGCCAACAGCTTT | 5607 |
rs117921322 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721918 | TGATGCTTTCGTTAC[A/G]TTTATTATCCCATCT | 5607 |
rs117958930 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659291 | TAGTAAACAATTGCT[A/G]AACTAAAGGCACGAT | 5607 |
rs117989463 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690094 | ACAGTTCTTCTTCCA[A/G]TGTGGCCCAGGGAAG | 5607 |
rs117997171 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543571 | CCAGTGGCAATGGCT[A/G]CTGCTGGCTTCCTGT | 5607 |
rs118010783 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587578 | ACTTTATCAGCCAAC[A/G]CAGCTCCTTCCCTTT | 5607 |
rs118023567 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681729 | AGGTTTATGTGTTGC[A/G]GTAGAAGAAACTTAT | 5607 |
rs118035854 | snp | A/G | 0.237593 | 0.249692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582631 | TTGAGACCAGCTTGG[A/G]CAACATGTCAAAACC | 5607 |
rs118036636 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643108 | GCCTGCACCTTGGGA[A/T]TTTTTTCAAGTGCCC | 5607 |
rs118048150 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736214 | AATTGGGTTTGAGAA[C/T]TTTGTACATCCCCTT | 5607 |
rs118052550 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647027 | TATTACGGCAAAATA[C/G]AGATTTCTAGGGACA | 5607 |
rs118134506 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565231 | ATGTCATCACTGTTA[C/T]TTATTTTTTTTTCTC | 5607 |
rs118150125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770565 | TTTCCCTCCTTCACC[A/G]AAGTCCAGAGTCATG | 5607 |
rs118165148 | snp | A/G | 0.081446 | 0.184634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729814 | TGACAAGTGAAGCAC[A/G]TGAAAGCTGTGGTCA | 5607 |
rs118188424 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666835 | CAAGTCCTTTCAAGG[A/G]ATTTCAGTGAATGAG | 5607 |
rs137874165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625935 | TCCAGTATGGTATGT[A/T]TATTAGACTATCTGC | 5607 |
rs137904882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550324 | TAATTACCAGCATGA[C/G]CTTTATCTGCTCTTG | 5607 |
rs137915138 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758480 | TTCCTGCTCCAGATT[C/G]AATTATGAGTTTAAC | 5607 |
rs137962712 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805850 | ACTGTGGCCTGGTAA[C/T]CCTGGGGTTGTCCCT | 5607 |
rs137966252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725124 | AGCACTGGCACCTGT[G/T]CCCAAGCAGACTGGT | 5607 |
rs137985019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634975 | ATTTGTTCTGCCTGT[A/G]TGCCCCCTTTTTTAA | 5607 |
rs137988544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594149 | ATCCTATATACAGCT[A/G]AGGAGAATCTAGTGT | 5607 |
rs137995771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793850 | ACTGTTGAGGTTTTA[C/T]TTTCTGAGAGGACCA | 5607 |
rs138023101 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637613 | GTACAGATCATTCAT[A/T]ACTCAGCTGAAGACT | 5607 |
rs138026712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565765 | GTCATCTATCTCATT[A/G]ATGAGATAATTTAAA | 5607 |
rs138027497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650773 | TCATATTTATGAGGG[A/T]CATTGGTCTAGTTTT | 5607 |
rs138030503 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621333 | GTAAAGAATAACTGG[C/G]TATGATATGCTTAGA | 5607 |
rs138089792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674521 | ACAAACTCTGACTCT[A/G]GGTTGTTGGTTTTTC | 5607 |
rs138099492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628930 | GTAATAATGGAAGCA[A/G]TTTTGGAGGTGGTGG | 5607 |
rs138101245 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586864 | AATACTCGGGCCGGA[C/T]CCTCTCAACACAGCA | 5607 |
rs138101432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720032 | GAAATCAACATGGAA[C/T]GGTTAAAGTGTCTGT | 5607 |
rs138135614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589985 | GTCATCACTTGATAA[A/C]TAGCAGCTGCTATTA | 5607 |
rs138141425 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654957 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCTG | 5607 |
rs138143099 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581151 | GGATATTTATAAATT[A/G]TGGCTCATGATGGTG | 5607 |
rs138158504 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777899 | ACAGGATGCAGTTTG[C/T]AATTGAAATTTGACA | 5607 |
rs138159760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751507 | CTTTATAAGTGATGT[A/G]TGTCTATGTGTACCT | 5607 |
rs138181079 | in-del | -/ACA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762564 | TCTTTTAAATGACAG[-/ACA]AAAAAAAAAAAAAAA | 5607 |
rs138204974 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608160 | AAGAGATCTAATTTC[C/G]ATTTGAATCTATTCC | 5607 |
rs138206068 | snp | G/T | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617959 | TCAGCCTCCCAAAGT[G/T]TTGGGATTACAGGTG | 5607 |
rs138248513 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567124 | GTCTTTTAAGAAAAT[A/G]TAAAGTAATTTGGTC | 5607 |
rs138248552 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611096 | CTGATTCTATTACGA[C/T]GGTTAACTGTAGCAG | 5607 |
rs138268979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735136 | AATTGCCAGTGTCAA[A/G]TTCTTCTCCATATCT | 5607 |
rs138301511 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731359 | CCCTGGGAGCAACAT[A/G]AAGGTTAAAGGGCTG | 5607 |
rs138364135 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617030 | CATAGAACAGTGGCA[A/T]TACTATCATTTCAGT | 5607 |
rs138371349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739988 | AGGGGTTGGAAGGAT[G/T]GGGGGAAGCTGTCTT | 5607 |
rs138402057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621203 | AAGTATTACTAGAGA[A/G]ATGTTATGAAAATAC | 5607 |
rs138417718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766551 | AGTCTCTGAACTCCT[C/T]GGGATGACTAGATAC | 5607 |
rs138424226 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687533 | ACAGGGTCTTACTCA[A/T]GTTTCTCTCCACAGC | 5607 |
rs138458050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700120 | AAGGGATATACCTTG[A/G]TATCTTCCTGCTTTT | 5607 |
rs138464237 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772001 | CACATAGCTAAGTAC[A/G]TGTTACAGCTACTAA | 5607 |
rs138465895 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690670 | TCCCGAGTAGCTGAG[A/G]TTACAGGTGTCCGCC | 5607 |
rs138477251 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555097 | CTCACCTTTTGGGCT[A/G]ATGGTCCTAAACCTT | 5607 |
rs138488138 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571556 | TTCTTCTATGTACTC[G/T]TACTTGGAAATGAGA | 5607 |
rs138516014 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724154 | ACATATCTGCAGGCC[A/G]TTTCAGAGAAGATTA | 5607 |
rs138521028 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675764 | GTCAGCTTAATCAGA[A/G]AAGGTTGTCCTGGAC | 5607 |
rs138540364 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593303 | TCTTTCATTATCTTT[A/G/T]GGGAGAAAAGGAAAA | 5607 |
rs138540541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544551 | TGTTTCATTGACTTA[A/G]TAGGTTTCTTTCCCT | 5607 |
rs138555086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716319 | GCACTCCAGCAACCG[A/G]GCAAGACTCTGACTC | 5607 |
rs138577099 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701943 | GCTCCGCTCCTGGAC[A/G]GTGCATTTAATGCTA | 5607 |
rs138584859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799325 | GTGCAAGCACCTCCT[C/G]TCACCCCTGTGCCCT | 5607 |
rs138586081 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586449 | ATTTTTTAGTGAATA[A/G]GAAACATTCTACATA | 5607 |
rs138592208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766659 | TAACAAAATAGGCAG[G/T]TTCTTGGAGATCTTT | 5607 |
rs138594154 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687698 | TGGGAAAAGATGGAG[C/G]TCCTTCTCAGGCCAA | 5607 |
rs138597079 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782939 | TCCTGTGCAGGCAGC[A/C]GTGCTGCATCATCTG | 5607 |
rs138611362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803106 | ACAGTGAGCATGGGA[C/G]CCAGTGGGCACATCA | 5607 |
rs138620205 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720458 | GACAGCAGGGTTAGA[A/G]AGACCAAGAAACATT | 5607 |
rs138620743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761352 | CCTTCTGTCTGTCTA[C/T]TTTATGAAACCAACT | 5607 |
rs138652422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625307 | GTGTATGTGTGTGTG[C/T]TCAATTTTAAGGGCT | 5607 |
rs138701671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704774 | GAAACTAGTGTTTTT[A/G]ATTTGTGGGACTCAG | 5607 |
rs138705732 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734716 | CCTAAAAAGTTTGCA[C/G]TCTTTGAAAAGAGGT | 5607 |
rs138712000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615795 | AGGTGACATCTAGAG[A/G]GTTTTAAAATTAATC | 5607 |
rs138735800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574941 | AGAAGAGAAGAGAGA[A/T]GGTTTGGATTACTTC | 5607 |
rs138740810 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601923 | TCCTTTAAGAACTTA[C/G/T]GTTCACATGTTTGGA | 5607 |
rs138744565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681188 | AGGAAGATCAGATAT[C/G]AAGATATCAGATATC | 5607 |
rs138765899 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549083 | GCGGCTTTGTCAGCC[A/G]GCTGCCTGGTGCCAG | 5607 |
rs138810660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663477 | CATTCAAGTTAAATC[C/T]GTTACTCAAGATGTA | 5607 |
rs138812056 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572233 | CCTGTGATTCAGTCT[G/T]TATGGACAGTGACGG | 5607 |
rs138812764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751132 | GCCACTCTGGGAGTC[A/G]GGAGGTGGAATCATG | 5607 |
rs138844598 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778636 | TGGAAAAGGATCTTA[C/T]CTCTGTGAGAGCAGG | 5607 |
rs138885336 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793301 | AAAAAACAAAAAATT[A/C]TTTAGCTCATTATTA | 5607 |
rs138910641 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570461 | AGTCTCCTCATGACA[A/G]GAGCAATGAGTTATT | 5607 |
rs138911722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701261 | CAGACATGAATAGCA[A/G]TGTATGAGGAAGTTA | 5607 |
rs138911936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782525 | GCGCCTCACAGTAGG[C/T]GCCTCTCTTCTCACA | 5607 |
rs138926989 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691732 | ATTGTTGTCACTGAC[A/G]ATGCTTCACAGAAAT | 5607 |
rs138976479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656826 | ACAGTTGCCATTTTT[C/G]ATAGATCTGTAGAAT | 5607 |
rs138978290 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745391 | GAGGACCCTTGGTTC[C/T]ACTTTTAATGTGCTA | 5607 |
rs139000505 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649993 | CACAGATGTCTTTCA[A/G]CTTACTTAGGTCTTC | 5607 |
rs139011684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658241 | TTTAATAGTCATATT[C/G]ATCTTTATAATTTTG | 5607 |
rs139028529 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583628 | TACTGGGTATATTTC[C/T]TGTGTCTACCTAGTT | 5607 |
rs139042532 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780030 | CCTCCCTGCGGCTTT[C/T]CCCTACTCTTCGACT | 5607 |
rs139160387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585058 | ACAGGAAAACGACAT[A/G]TACATCTGAGAGAGG | 5607 |
rs139165334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619109 | GCACACATTTCCACC[C/T]TGGGCTTTTGAACTT | 5607 |
rs139165411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676044 | GCAGACTGTGTGATC[A/G]TTGTGTGTTTTGGCT | 5607 |
rs139167187 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540837 | CTATGAAGAGCTGAC[A/G]TGTAATTATATTGGC | 5607 |
rs139178321 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640197 | ACGAGTAAGTGTTCA[A/G/T]TACATAATTTGTTGA | 5607 |
rs139196381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733231 | GATGTTTATACAACC[A/G]CCAGCGGAATTTTTT | 5607 |
rs139235821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638127 | TTGTTATATAAGTAT[A/G]CTTGTGCCATGGGGG | 5607 |
rs139274176 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598567 | AGTGTTGGATGCTTA[C/G]TACTCCTTGTTAGGT | 5607 |
rs139289332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645062 | CTGAGACACGAGAAT[C/T]GCTTGAGCCCATGAG | 5607 |
rs139301866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768329 | CACGCATATTGCAGA[A/G]GTGCTTTTATCATCT | 5607 |
rs139325807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692286 | CAGAAATCGTTGAAC[A/G]TGGAGGAGTTAAGAC | 5607 |
rs139349039 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587582 | TATCAGCCAACGCAG[C/G/T]TCCTTCCCTTTTTTA | 5607 |
rs139359626 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784310 | AGTAGGCAGAGGATT[A/G]TTATTGTGGTTTAGA | 5607 |
rs139383200 | in-del | -/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547172 | CAAATACTATTGGCT[-/G]GTTTATGTCTTTTGT | 5607 |
rs139387851 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763491 | TGTTACAGCAGATAT[A/G]TACATTGAGGACCTT | 5607 |
rs139401218 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725405 | CACTCCGTTTTAAGC[C/T]GTCCATTTACCATTG | 5607 |
rs139434143 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717625 | GATTCTGTGGGTCAG[A/G]AATCCTAGCAAGGCC | 5607 |
rs139434224 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626976 | CTCGCTCTGTCACCC[A/G]GGCTGTAGTGGAGTG | 5607 |
rs139442924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689148 | TAGTCCCTTTGACTC[A/G]GGAGGCTGAGGCAGA | 5607 |
rs139447034 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769198 | AATAAAAAGGAAAGT[A/G]TAAATAAATAGCAAA | 5607 |
rs139454779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618775 | CAAGAAGCTGACCAC[A/C]TTTCATCACTGTTTT | 5607 |
rs139471491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746112 | AGTTGACTTAGACTA[A/C]GCTTTTAACCTGCAA | 5607 |
rs139472847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706409 | AAGTGTCAGCATTGA[A/G]TGTGGGACACCTGAA | 5607 |
rs139479607 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697095 | ATGGATGAGCAAATA[C/T]TCAGAAATAGAAGGC | 5607 |
rs139491783 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658601 | AACATGTCCTTGGAA[A/G]AATTGCAGTAGCAGT | 5607 |
rs139510082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562798 | GGAGGTATTGCATAT[A/G]AAGCATAGATCACAG | 5607 |
rs139532294 | in-del | -/TG/TGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637911 | TGGAAGCCTGTTGAT[-/TG/TGTG]GTGTGTGTGAGTGTG | 5607 |
rs139532502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752136 | AGTGGCACAACCTCC[A/G]CTCACGGCAACCTCT | 5607 |
rs139559912 | in-del | -/CTAAAAGCC | 0.0252325 | 0.109451 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757362 | GATGTTCACACATTT[-/CTAAAAGCC]CTTGACCCCTTTATG | 5607 |
rs139580843 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688737 | ATATTGACAAGGTAA[C/G]TGTTATCTCCCTACA | 5607 |
rs139583039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599627 | TTCCAAGTGATATTG[A/T]ATTAAAAACTCCATC | 5607 |
rs139586150 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555725 | CTGTTTTATTTTATA[-/T]TTTTTAAATTGTAAA | 5607 |
rs139586159 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742137 | CCCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 5607 |
rs139597450 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692763 | TAATGACAGTAAAAA[C/G]TGCTGATATTGTAAT | 5607 |
rs139621390 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558495 | GCAGCCAGAGTGATT[C/T]TTTTAGAAGTCAGGT | 5607 |
rs139627122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604471 | AAAGTAGAGAATAGT[A/G]TGTGTTGTGGTTAAG | 5607 |
rs139651814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692015 | TATGACCTGTTACCC[A/G]TAGCATATGAATGCT | 5607 |
rs139672899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666171 | GTTAGGATCATCCTG[C/T]CTCTGGGCATACAGG | 5607 |
rs139682919 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744838 | TTTCTAATTGCTAAT[-/C]GATGGTCCTTGTAAG | 5607 |
rs139718463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752373 | TTTGCTAAGGTCACT[A/G]TCAGGAGTACAAAGA | 5607 |
rs139725800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702590 | CTAAATCCTAGAGGG[A/G]TAGATAGATCAGGAA | 5607 |
rs139730027 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613399 | AATGTTTGTTTCATT[C/T]GGTCAGAGAGATTAC | 5607 |
rs139734890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727254 | TTCCTGGTTGGATCA[C/T]TTTGTTTTTACAGGT | 5607 |
rs139749612 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609213 | GGTGTTGCTTGGTTT[C/T]GTTTAGTCTATATTC | 5607 |
rs139757379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795357 | TTTTTTCCTAATATA[A/T]GCCTATAAAGCTATG | 5607 |
rs139765361 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807315 | GAGAAACAGAAGCAC[A/G]GAGGCATTGGGATGG | 5607 |
rs139767818 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572949 | GATCTGCCTGCCTCG[A/G]CCTGCCAAAGTGCTG | 5607 |
rs139770864 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658900 | CTTCTGAAAAAAAAA[G/T]GCTGTTTTTTGTTTT | 5607 |
rs139798818 | in-del | -/ATG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757797 | ACGATATGGTATTTA[-/ATG]ATGTTTGTAGCCATA | 5607 |
rs139820111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685081 | AAATTTGGTGAAGCC[C/T]GTAAGTCCACAGATC | 5607 |
rs139846928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583909 | GTGCCACCACGCTGG[A/G]CATTTTTTTTTAATT | 5607 |
rs139855908 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623250 | ATTAACACCTGAATG[A/G]CGTACTTACCACACC | 5607 |
rs139867239 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587315 | AGGAGGTAGACAGGA[C/T]TTATCATGCGGGGCC | 5607 |
rs139890731 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665428 | ATTTTACACATCTGC[C/T]CATCTTAGCTGTATG | 5607 |
rs139908385 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591346 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAGTAGA | 5607 |
rs139926538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732771 | ACCTGGAGGCTGTAC[G/T]AGATTTTGCTGTAGT | 5607 |
rs139966646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774602 | CATCCTAGGGGCCCA[A/G]TCTAAAGGAACCAGC | 5607 |
rs139978558 | snp | A/C/T | 0.00914647 | 0.0670416 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804170 | TGCCTCTGGACAGCA[A/C/T]CTCCTGCTCTCGGGT | 5607 |
rs139985238 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727666 | ATATTACTAAGGGAA[A/G]CCACATAAGGATAAT | 5607 |
rs139993494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562456 | AATAAGAGAAGTATC[A/G]TGAAATAAATACATT | 5607 |
rs140010508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721408 | TTAAGGCGCACTCCT[C/G]ATGGGACCCTCACAT | 5607 |
rs140012695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804814 | CTCCTGAGAGGAAGT[A/G]TGCACGCTTGGACTT | 5607 |
rs140017624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758775 | CTTTCCCCACAACAC[A/T]CTATTTTACAGACAA | 5607 |
rs140026096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677096 | AGAAAATTAGCCTGT[A/G]AGTATAAAGAACTTA | 5607 |
rs140054791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695719 | AATGTACAAATCCAG[A/T]TTACAGTTGTCTTTC | 5607 |
rs140062248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563920 | TTACTGAAAATCTGC[C/G]TTAACAGTTATCTGA | 5607 |
rs140065938 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630439 | TCTGCATGTGTAATT[A/T]AAAAAATAAGCAAAA | 5607 |
rs140073009 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556637 | GCTCACTGCAACCTC[C/T]GCCCCCTGGATTCAA | 5607 |
rs140101662 | snp | C/G/T | 0.0107334 | 0.0725574 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638657 | CACTGCACTGTCTTC[C/G/T]ACAATGGTTGAACTA | 5607 |
rs140138070 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712681 | CCCAACACTTTAGGA[G/T]GCCGAGGCAGGCGGA | 5607 |
rs140140506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794942 | TTAAAACTATGATGA[C/T]AGGACTCTGAAACCT | 5607 |
rs140145930 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648732 | TGGGACTACAGGCGC[A/G]TGCCACCATGCCCAG | 5607 |
rs140146968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684382 | ACTAGCCCTGTAGTA[A/G]TGGTTACTCTCAACT | 5607 |
rs140190932 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771307 | TCACCCTCTCTGCTC[C/T]GGAGGAGATGTTGGA | 5607 |
rs140197724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790861 | CTGATAGTTATGACT[A/G]TGGAACTGCCTCTGG | 5607 |
rs140202181 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579217 | CCTGAGCAATGTTCC[-/A]AATAGCCACTGGCAT | 5607 |
rs140221212 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805494 | TAAGCAGCCTCTCTA[C/G]GGCTGCAGTCAAGGC | 5607 |
rs140228745 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724748 | ACCTAGAGGGATAGA[A/G]GCATACATAGAAGGC | 5607 |
rs140228997 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634438 | ACTGTATAGGGTATT[A/G]TATAATGTCAATTAG | 5607 |
rs140239677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761556 | TTTTAACTAACAGTC[A/G]AGTGAACATTCAGGA | 5607 |
rs140243816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681359 | TGTGAGTACACACAC[C/G]CACACGTACATGTAT | 5607 |
rs140262013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802036 | GCACCCACACACTGC[A/G]GCAGGCTCGGAGCCT | 5607 |
rs140275804 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589299 | TCATTCATTATGCTA[C/T]TATCTGGCTATCAAC | 5607 |
rs140276837 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647821 | TTGCAGTGAACCAAG[A/G]TCGCGCCACTGCACT | 5607 |
rs140320277 | snp | A/C/G | 0.0142988 | 0.0835604 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788703 | AAAATTTGGCCAGAC[A/C/G]TGGTGGATCATGCTT | 5607 |
rs140333956 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558684 | CATTCTGTTCTAGCC[A/T]CTCTGGCTTCCTTTC | 5607 |
rs140351574 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633083 | CTCACTGAATGCAGC[C/T]GTGTCATACCACCTT | 5607 |
rs140371331 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686736 | AGGCTGGGGGTCAGG[G/T]TAGAACTGACTGTAA | 5607 |
rs140437198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783465 | GAACTTCTCCACCTC[C/T]GAAACCCAACTGGCA | 5607 |
rs140450540 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628341 | AAAAATTAGCTGGTC[A/G]TGGTGGCAGGCACCT | 5607 |
rs140455574 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620461 | TAGTAATTTATAACA[C/T]GAACATATAAGGCAA | 5607 |
rs140456739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707767 | CACTAGGAGAAAGAG[A/G]GAAAAGATAGAGGAT | 5607 |
rs140473016 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785814 | GCAAATCAGTCTATC[A/G]TGTGAATGTGAGCCA | 5607 |
rs140516002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753968 | CAGAAGTTCACATTG[A/G]ACTATAAATAGGAAT | 5607 |
rs140522458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791391 | TGGGGAAAGACTGAC[C/T]TGTGAAGGCCAAGAA | 5607 |
rs140528506 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650124 | TTCATTTTTGGATTG[G/T]TCATTGCCAGTGTAT | 5607 |
rs140528753 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733785 | TAGGTAGATAATAAG[-/T]GAAAAATATGCATTC | 5607 |
rs140563758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703761 | AAATCTGGAGAACCC[A/G]TGATGTAAAATAGGG | 5607 |
rs140568177 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742056 | TCTGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 5607 |
rs140592767 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776432 | TTCAGAAAAATGCAG[G/T]GATTCCATGGCTTAT | 5607 |
rs140623635 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590442 | CTCTCTCTCTCCCTC[C/T]CTCCCTCTCTCTCTC | 5607 |
rs140652772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614792 | AAGGGGTATATAGCC[A/G]GAGTAAACAGAAAGA | 5607 |
rs140692589 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654829 | ACTTTGGGAGGCCGA[A/G]GTGCGCGGATCACCT | 5607 |
rs140693156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627163 | TATGTTGCCCAGGCT[G/T]GTCTTGATCTCCTGG | 5607 |
rs140716687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743430 | TACGTGTTCACCTGA[A/C]ATTATTGGAAGTAGT | 5607 |
rs140726826 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718679 | TGAGGCAGGAGAATC[A/G/T]CTTGAACCTGAGAGG | 5607 |
rs140737301 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767387 | TTGGTAAATATTGAA[C/T]GACATTAAGATAGCA | 5607 |
rs140741319 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660438 | GCTGTGGGCTGTGGT[A/G]TGTAAACTAAATATT | 5607 |
rs140752928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697576 | TATTCTGCTCACTCT[A/G]TATATCCAGTACCTC | 5607 |
rs140753401 | in-del | -/AATAATAATAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686604 | TGAGACTGTGTCTCA[-/AATAATAATAAT]AATAATAATAATAAT | 5607 |
rs140776574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729350 | ATTTCTCAAACAAAT[C/G]TTAGTAGAAAACTTA | 5607 |
rs140790871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687375 | ATTGTCTTTATTAAA[A/G]GAAACATCCCTATTG | 5607 |
rs140802875 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770630 | AGAAGAAACCCTTGG[C/T]TCTGTGGTGTGGCAA | 5607 |
rs140812304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760744 | TCTGTGAATGGGCAG[C/T]TGCCTGGTGGGGCCA | 5607 |
rs140816025 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548431 | CGAAGTAAGCTTTGT[A/G]ATATTCCAGTTATTG | 5607 |
rs140841586 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624945 | CAAACATCACCATCT[A/G]TTTCCTTTAGGTCCT | 5607 |
rs140843235 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764201 | AGATATTTGAGAGGT[A/T]GTCCCATCTTCCTTT | 5607 |
rs140869674 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | MAP2K5 | GRCh38.p7 | 15:67727925 | TCCCAGCTTGCTCTT[A/G]GGAGGTTTCCATATC | 5607 |
rs140872026 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805300 | CAGCCTAGGATGAGG[C/T]GGCCTGAGCATTCTC | 5607 |
rs140877548 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567537 | GCCCGGCTAATTTTT[C/T]GTATTTTTAGTAGAG | 5607 |
rs140885182 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564431 | GGTTGTAGGTTTTTG[A/G]TAGACTTCAGCTTCA | 5607 |
rs140911653 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595936 | ACAGTTACTCCAAAG[A/G]TATGTGAGTTTGGCC | 5607 |
rs140912431 | in-del | -/TA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740216 | AGAGTCTAGTATAGC[-/TA]GCCTGGCATAGCATA | 5607 |
rs140919067 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796194 | TGAGTTTTTTGTACA[A/G]TCCTATTTTGTACTT | 5607 |
rs140949961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662278 | CTCCCATTGCATTTC[G/T]TATTTCACAGTTGCT | 5607 |
rs140968240 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543658 | GGCAAATGTCTAGGA[C/T]CCTGGGGAGATAGAT | 5607 |
rs140983819 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597667 | CTAAATGAAAAAAGC[A/G]GAAATACTACTGGTT | 5607 |
rs140984803 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721074 | CCTGTTTAAGTGTCT[A/G]CTGTAATAAGCCCAT | 5607 |
rs140987313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631617 | CAGGCTACACACAAC[C/T]CAGGGATGTTCCAGG | 5607 |
rs141028376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591161 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 5607 |
rs141054579 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743033 | TGAGGCCAAGTAAAC[A/T]AATTTATGGCTGTGA | 5607 |
rs141065417 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634046 | CTCAGAATATGACCT[A/G]TTTTGGTAAACAGTC | 5607 |
rs141095781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734533 | TAATGTTGAAGTACT[A/G]GAGTTTTTACACTTA | 5607 |
rs141100336 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565365 | CTCCTGAGTAGCTGG[A/G]ATTACAGGCACCCAC | 5607 |
rs141103759 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723617 | TCTCTACCTCCACCC[C/G]CTGGCCCCAAATAAA | 5607 |
rs141119445 | in-del | -/ACAC | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720304 | AGTATACACATACAT[-/ACAC]ACACATATGCTTATA | 5607 |
rs141137265 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757877 | GAGAGAACTCAGTGG[A/C]GGAGATGGGGGCTAC | 5607 |
rs141156744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710438 | CATAGGTAAAGAACA[C/T]AGTCAGAGAACAACA | 5607 |
rs141161022 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593491 | AACCCAGCCAGTGAG[C/G]GACAAACAAGCCTTC | 5607 |
rs141180758 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602945 | GAGTGAGCCACCAGA[C/T]CTGGCCAGGTTTATT | 5607 |
rs141185073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743952 | TCTTTCTTACTCCAA[A/G]GTTCATGCGTTTTCC | 5607 |
rs141202355 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608690 | AAGGGCTCCATGACA[-/G]CTGACTTAAAGTCTG | 5607 |
rs141219510 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737447 | TTTAGATGTTTAACA[A/G]TTATGGATTAATGCG | 5607 |
rs141225837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690511 | GAGACCAGGGACTTG[C/T]TGGTAAAGGGGACAT | 5607 |
rs141226594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700489 | GCTAAATATCCATCA[C/T]AGATATTCTGTCAAC | 5607 |
rs141259581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705586 | CTAAAAATACAAACA[A/G]TTAGCTGGGTGTGGT | 5607 |
rs141265002 | snp | G/T | 8.25852e-05 | 0.0064254 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693582 | CGGTAAGTAAACTTA[G/T]GCAAAAATAATGTTT | 5607 |
rs141271055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606316 | CAGATAATCTAGTCT[C/T]AAGATGTTTGAAAAC | 5607 |
rs141288338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786738 | GTTACTGAACGCTCT[C/G]CACCTCTAGTTGCTT | 5607 |
rs141291231 | snp | A/G/T | 4.94624e-05 | 0.00497284 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580811 | ATAGAGCCTCTGCAG[A/G/T]TATTTCCAAGAGGTA | 5607 |
rs141298860 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583335 | GGAGAGGATACTTAA[A/C]GGAGGAAATTATATG | 5607 |
rs141334128 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755849 | AAAGTCTGTTTCCAT[C/G]TTAAGCAAATCCACT | 5607 |
rs141337705 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579719 | AAAAACCCTTGCTCT[C/T]GTAATAATTTTAATG | 5607 |
rs141360856 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652657 | AAATATTCAAACTGT[A/G]TCAGCCATTTTAAGT | 5607 |
rs141385762 | snp | A/G | 6.68259e-05 | 0.00578001 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646401 | AGTGCGATTCATCAT[A/G]TATCATTGGATTTTA | 5607 |
rs141413615 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798521 | GCTGCTCTGTAAGTA[C/T]AGGCCCTAGAATGAC | 5607 |
rs141461366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649092 | GTGGGCTTGTAGTGT[A/G]ACATGGTATCCCATT | 5607 |
rs141463045 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701501 | TTTAATGAAGTACAG[A/T]AGCAGGAATTTATAA | 5607 |
rs141465920 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611794 | ATTTTGGCTCTAAGA[A/G]GAGCTAGAATAAACA | 5607 |
rs141477506 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574799 | TTGAACCTGGGAGGC[A/G]GATGTTGCACTGAGC | 5607 |
rs141486325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572403 | TTATCGGAAAGGGGT[C/T]CCAATCCAGACCCTA | 5607 |
rs141506619 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763314 | AAAATAAACTCAATG[G/T]TTTAACAAGCATTGA | 5607 |
rs141526306 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626964 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCCGGGC | 5607 |
rs141550861 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544865 | TTTGGGTGCCTTGAC[C/G]AGGAGCTTTCCATAT | 5607 |
rs141575734 | snp | A/G | 0.25045 | 0.25 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695122 | TGTGGGTTGGGGGGA[A/G]GGGGGAGGGATGGCA | 5607 |
rs141595381 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638209 | GTTATTTTTCCTGAT[A/C]ATCTCCCCACTTCAC | 5607 |
rs141599099 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566753 | CAGTACAAGTGTACA[C/T]TTTTATTAGTAATTT | 5607 |
rs141609086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586150 | ATTTTCAATTATTTG[A/G]AATTGTTTTGTTGGT | 5607 |
rs141613784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799255 | GGAAAACTCTGCATT[C/T]GTGGCATTTGCCCAG | 5607 |
rs141617893 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554709 | CATTACATTTTGAGT[C/T]ACTTAGTGATAGGTA | 5607 |
rs141628200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665829 | CTCTGAGTATAAATA[A/C]GTGTGTAAACAAATT | 5607 |
rs141631780 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621312 | TAGGTTTATATACAC[A/C]CCTTAGTAAAGAATA | 5607 |
rs141633165 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751888 | TTGAAGTGTATAGAG[C/T]CCTTTGCCCCCAGGC | 5607 |
rs141640175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662568 | CTCATGTGCATATAG[A/G]ATCAGTGGTTATGAA | 5607 |
rs141640383 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801456 | TCACCCTGAGGCAGA[A/G]CAGTCCTGTGGTCCA | 5607 |
rs141670905 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675834 | ATCATAGGCAGAGTC[A/C]TCCCTTTTAGGAAAT | 5607 |
rs141679994 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670899 | TTCTGTAGTTAAGCC[A/G]ATTTTTTTCCCCAGA | 5607 |
rs141696163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588435 | TCTCTAGGAATTCCT[A/G]TGATACTCCCTTCTT | 5607 |
rs141739936 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744462 | AACTGATATTGGAAG[A/G]TCTGACCTAGGTCAC | 5607 |
rs141754151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734025 | TTTGATTACCAATAA[C/T]ATTTGTTTGATTTGG | 5607 |
rs141784505 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618013 | TTCCTTACCTTTAAA[G/T]ATTATTCTAGAAATT | 5607 |
rs141792015 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735668 | ACTTCAGGAAACCAA[C/G]AGGGTTTCACAGAGT | 5607 |
rs141802899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625497 | AAAACATTGCAGAGG[G/T]GTATAGTTGTCTTTT | 5607 |
rs141804835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549441 | GGGTTTATATCGTCA[G/T]GGAAACTTGGGTGTC | 5607 |
rs141815568 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684273 | AGTTGGGAATATTTT[-/A]AATTCCAATAATCCA | 5607 |
rs141828291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545959 | GTACCTGGCTCAAGG[C/T]TGACTGGCTTAACAG | 5607 |
rs141847611 | in-del | -/TG | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596511 | AAAAAGTTTAAAAAC[-/TG]TATCATTACTAGTAT | 5607 |
rs141891478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650587 | ATCTATTGAAATAAT[C/T]GTGCATATTTGGTCC | 5607 |
rs141918877 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734773 | ACTTTTTGAAGTTTG[A/G]AACATGAAGGATTTA | 5607 |
rs141921379 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803893 | GCAGTGGGTTTGGGT[C/T]ACAGACTTGTGGTTC | 5607 |
rs141925262 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720990 | CAATCATTTTTAACA[C/G]TGAAACAAATAAAGC | 5607 |
rs141951312 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676164 | AAGCCCCGCAGTTAG[C/T]TCTGATCATTGCTTT | 5607 |
rs141954416 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590668 | ATGTTGCCCAGGCTT[G/T]TTCTTGAACTCCTGG | 5607 |
rs141970699 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604272 | TACATGGAACATAAA[A/G]GAAATACCTTAAAGT | 5607 |
rs142006080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643058 | AAGATGTGGGCCCAA[C/T]CCAAGGGATTCTCAT | 5607 |
rs142015605 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637712 | TTCTCTAGCTTCCTT[G/T]GCCTCCTCAGACTCT | 5607 |
rs142016857 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732192 | GGACTGGAGCTGCCT[A/G]TAGTTAATCATGTAG | 5607 |
rs142019706 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565979 | ACCATTTGGACGTAA[A/C]CTTACAGTAGGTTTT | 5607 |
rs142026534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603408 | AGCTCATTTAGCTAC[C/T]GTTGCTAATGCTCAC | 5607 |
rs142044342 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581665 | ACTGTACAAATAATC[-/A]TGGTATGAGTTTTCC | 5607 |
rs142062997 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780835 | GGTTTAGCCATCCCA[C/T]CCTGGATGTATGGAC | 5607 |
rs142101193 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703603 | TATTTTAAAGCACTG[C/T]TTATTACAGATCACC | 5607 |
rs142110071 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614341 | TATTAGAATAAGGAG[A/G]TTTTCTGAAGTAGCC | 5607 |
rs142110803 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641216 | TTAGCATTGTATATT[C/G]CATGTGCCAATTATC | 5607 |
rs142129671 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573422 | GGGCGGGAGTTGCCA[A/C/T]ACACTTTTAAACCAT | 5607 |
rs142141484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793083 | GAGGTCTTAAATGTG[C/T]TATAACACTGCTCTA | 5607 |
rs142152033 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639245 | ACAGAGTTCTAATAT[A/C]CCTTTCTTTTCCTTA | 5607 |
rs142152593 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716735 | TCTGATGTGAAATGT[A/C]GTGCTCTTTCCTCTC | 5607 |
rs142174071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714000 | CAGTTTCTTATGTAT[A/C]AGTTGAAGGTAACAT | 5607 |
rs142192154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718833 | GATATTTTGATACAG[G/T]CATACAATGTGTAAT | 5607 |
rs142195400 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799453 | CCTTACAACCCACTC[C/T]GGGAGGAAGAGAGAG | 5607 |
rs142201712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607593 | GACTCAGTTTCCACC[C/G]GAATTAACTATTATT | 5607 |
rs142210677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779519 | TGTGTGTATGTATAT[A/G]TCTTTATATGCATGC | 5607 |
rs142212360 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696713 | CCAGGCACAGTGGCT[A/C]ATGCCTGTAATCCCA | 5607 |
rs142234722 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567655 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTAAAGTA | 5607 |
rs142239344 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605564 | TAATTTATTTTCAGA[C/T]TGCTATAGGACAGCT | 5607 |
rs142252426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800832 | GACCAGTGCACCACA[A/G]CAGCCCTCCTAGCCC | 5607 |
rs142258659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688326 | AGGCAAAGAAGTGAC[A/G]TGGTCTGACTTAGGT | 5607 |
rs142278620 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632160 | GCTGGAGTGCAGTGG[C/T]GTGATCTAGGCTCAC | 5607 |
rs142279660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558249 | GGCACTCTATGTGTG[C/T]TTCTGGAATGCATGG | 5607 |
rs142296324 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668924 | ACTTTTTAAAAATAC[A/G]TTTTTGCAGAAATTC | 5607 |
rs142332015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584863 | CACCATGCCCAGCTA[A/G]TTTTTTGTATTTTAG | 5607 |
rs142366502 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587109 | CTCTGGGGAGAGTGA[C/T]GTTTCTGTTTTGACC | 5607 |
rs142383453 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621210 | ACTAGAGAAATGTTA[C/T]GAAAATACAAATATT | 5607 |
rs142424210 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747900 | TAGCAATGATTGCAA[C/G]ATTAAGCCCAGTGTT | 5607 |
rs142435531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712374 | CACAGTTTCCAGTGA[G/T]ATTTTCAGTGCCTTA | 5607 |
rs142435597 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762338 | CATGTAGGCACATCT[A/G]AAAACTGCTGTGCAC | 5607 |
rs142447687 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620319 | GAGGTTTCATTGAGC[C/T]GAGACTGCACCACTG | 5607 |
rs142460464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713385 | TTGTGATCTTCTATA[C/T]GTATAAGTAAACACA | 5607 |
rs142483822 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626050 | TTGAATCCTGTGTAT[A/G]TATTTAATTATTTGT | 5607 |
rs142495458 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609697 | CTGTAGACCTATTCT[A/T]TAGGTCTATAGAATA | 5607 |
rs142540454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545329 | TGTTTCTTCATAGGA[C/T]CCCAAAATACTTGTT | 5607 |
rs142549463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775917 | CAAACAGGCAACATA[C/T]TCACCACCAGCTGGG | 5607 |
rs142550156 | snp | C/G | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543345 | CCTGTAATGCTGTGG[C/G]TAGCCCTTGGCCCCT | 5607 |
rs142554238 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742233 | CTGCCCAAAAGAGAA[A/T]CATTGGAATCTCATC | 5607 |
rs142554270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652401 | AAACATGGTGCCCAG[C/T]ACCTGTTTCTGGTCT | 5607 |
rs142567160 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586888 | CACAGCAGCCCAGCA[A/G]TCTCAGATTCACTTC | 5607 |
rs142575707 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775404 | CCAGGATACGTTTCA[G/T]CTGCTGTGGTTTTCT | 5607 |
rs142591586 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722404 | CACATTTAATTGAAA[A/C]CCTACTTCAAGACGC | 5607 |
rs142594536 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805034 | AGGGGTCCTGCAGGT[A/G]TGTCAGGAGCCTCCC | 5607 |
rs142605233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778669 | GATCCTTTGCGGTTA[A/G]CAGAAGGGTAGGGGG | 5607 |
rs142617082 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590355 | TCATATTAGGTCTTG[A/G]GTCCTTTCTCTTTTT | 5607 |
rs142625734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564317 | GAAAAGTTAAAAGTT[C/T]TATACAAATGCAAAT | 5607 |
rs142641358 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680194 | TATTCCATTGTATGG[A/C/G]TATATCACATTTTGT | 5607 |
rs142677132 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735847 | GTCCAGTCTGGCTTT[C/T]ACGTGGCAGCTTTGC | 5607 |
rs142718985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793456 | TAGATGTCATTTCTT[G/T]CTGCTGTTCTTGTTC | 5607 |
rs142732729 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695272 | AATGATAATAAATTT[A/G]AAAAAAAAAGATTTA | 5607 |
rs142764040 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635506 | TTAAAGACATTTAAA[A/C]AGTAAGAAAAATAGT | 5607 |
rs142773390 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560704 | TTTATGCAACTTCTC[C/T]TCAAGAAATTATTCT | 5607 |
rs142777037 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733218 | TCAGACTTGATCTGA[C/T]GTTTATACAACCGCC | 5607 |
rs142786548 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751283 | AACAGGAGAATTGAG[A/C]TCCAATCAGAAATCT | 5607 |
rs142789671 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567151 | GGTCTCCAAGGAGAT[A/G]TTTAATGTATTGAAA | 5607 |
rs142805121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596554 | AGATTCTTACAGTTC[A/C]TCTTGGATTGCATAT | 5607 |
rs142813743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617794 | CCTCCCAGGCTCAAG[C/T]GATCCTCTCACCTCA | 5607 |
rs142822824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795405 | TGCTTTAGCTGCATC[C/T]AACAAGTATTTACAT | 5607 |
rs142837062 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740293 | CAAGTTTACTTTTTA[C/T]ATGTTTGCAATCAGA | 5607 |
rs142837108 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692071 | TTACTATTACTTAGA[A/T]AGGAGGACTAGCTTG | 5607 |
rs142869512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745638 | TAAATTTTCTGGTGG[A/G]ATTAACAGAGGAACA | 5607 |
rs142879997 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657220 | CCATTGTCCATTTAG[G/T]TAATTAGGCCCTGAT | 5607 |
rs142889119 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608273 | GGTGCTGAGTTTACA[C/G]ACATATGGACAGTTC | 5607 |
rs142919254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612967 | GAAGACTTTGTACTG[C/T]AGTATTGAAGTGTTC | 5607 |
rs142947378 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790428 | AAAAATACCCTTTTC[A/G]TATCACACACTAATA | 5607 |
rs142952920 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767702 | TTTGCTCTTCAAACC[G/T]ATGGGACTTCTGTGG | 5607 |
rs142968494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661527 | AGTTCACAGATTTCT[A/G]GCTCCTTTTTCACCA | 5607 |
rs142969544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584152 | CATTGTTAAAAGATA[C/T]GTTAAATATTAATAA | 5607 |
rs142999294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758558 | TGCACCTAACATCCT[A/G]TAGGCTCTTGTAAAT | 5607 |
rs143005479 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690146 | GTTTAGGACATCAAT[A/G]TGTAAAAGAACAAAT | 5607 |
rs143005687 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770795 | CCTTTTTGACTAAGT[A/G]TAACATGTTACCTCT | 5607 |
rs143019232 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571803 | CTGAGGTCACTCACT[C/T]GCTGGTTTGTTTCCT | 5607 |
rs143032365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560170 | TAACTTTTCGTAGCT[C/G]TCAATTCACTGTCTT | 5607 |
rs143046602 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756763 | CTATTTTAGATTCTA[A/C/T]ATATTAAGTGAGATC | 5607 |
rs143051918 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634097 | GTATAGCCTGCTTGT[C/G]CCTGTAATCCCAGCA | 5607 |
rs143145748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750946 | GTTCAGACAAGATGG[A/G]TATATTTGGCGTCAC | 5607 |
rs143175371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729882 | TTCCTGAATGTCTAA[A/G]TATATCTTTACTTGA | 5607 |
rs143178344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684118 | GCTCTAGAAATTGCA[C/T]AGGAGTTCCCTTGCG | 5607 |
rs143219898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687553 | CTCTCCACAGCACCT[A/C]GTACCATATCTGGCA | 5607 |
rs143221095 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611516 | GGAAGATGCCAAGAG[A/G]TACTCAGAGTCACTG | 5607 |
rs143236924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598660 | AGTGGTAAAAAGACT[A/G]TGATGTCAGAATTAT | 5607 |
rs143296202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725551 | AATTATTCCATGGTC[A/C]CTGATGACATGCTGA | 5607 |
rs143323345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607247 | TATATGACTGGATTG[C/T]ATTATAGTATCGTGA | 5607 |
rs143338896 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806300 | GCCTCGGCTGACTGG[C/T]CGTGCGAGTGATGCC | 5607 |
rs143341514 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686571 | TCACATCACTGCACT[C/T]CAGCCTGGGCAACAG | 5607 |
rs143341786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566066 | TTTGTAGGTTCAATT[G/T]GGCTCTGAAGTTTGA | 5607 |
rs143343286 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732976 | GGGGGGCTTAACAGC[A/G]ACTGTGGGCGAATCT | 5607 |
rs143351884 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596159 | TTGTATTTGGCTGGG[C/T]GTGGTGGCTCATGCC | 5607 |
rs143381618 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688985 | TGAGCAAGATACTGT[A/G]CTCGGAAGGGATACA | 5607 |
rs143391355 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776202 | GACAGGTAGAACCCC[A/C]CCCCCACCCCCACCT | 5607 |
rs143392889 | snp | A/C | 0.0150606 | 0.0854603 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543031 | CACGGCGGCAGAGAC[A/C]TTCACCATAGCGTTC | 5607 |
rs143425685 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728820 | TAGATTATGCAGATG[C/T]ATCACAAACATGGTT | 5607 |
rs143428566 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637537 | ATTAATCTGGAGATC[A/G]TTTCTTCTGAGCCTT | 5607 |
rs143440559 | in-del | -/GGG/GGGGG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609069 | CAGAATGATGTGGCT[-/GGG/GGGGG]GTTGTTCAGAACTGC | 5607 |
rs143448322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597925 | AAAACACAGTCAGGC[A/C]GGGCGTGGTCGCTCA | 5607 |
rs143462292 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799038 | GCTGGGCATGGTGGC[A/G]GACACCTGTAATCCC | 5607 |
rs143465819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728376 | AATATATAGGCCCCC[A/G]ATTTTATGAGTGTAA | 5607 |
rs143470893 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783310 | CCCCGCTCACCTTCT[C/T]CTCCCACCCTCACCT | 5607 |
rs143489555 | in-del | -/AATAATAATAATAATAATAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686604 | TGAGACTGTGTCTCA[-/AATAATAATAATAATAATAAT]AATAATAATAATAAT | 5607 |
rs143539140 | in-del | -/CAGAGT | 0.225893 | 0.248835 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643468 | TTATTTTTTTTGAGA[-/CAGAGT]CAGAGTCTCGCTCTG | 5607 |
rs143552468 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592599 | CAGATGACATTGTCC[A/G]CATGAAATTGCCTCT | 5607 |
rs143569478 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792814 | CAAGGTAAACTTGGG[C/T]CCAAAGCGGCCCCGT | 5607 |
rs143613729 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664308 | AGACCAGCTTAGGCA[A/G]CATTAGTGAGATCCC | 5607 |
rs143636588 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656005 | AATATGCTGTTGATC[C/T]TCTCCAAAAATTTTC | 5607 |
rs143637268 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575193 | ATTAGTCTCAGTGAT[A/T]CCTCTGGTAGTTGAA | 5607 |
rs143654776 | snp | C/T | 0.237593 | 0.249692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582279 | GTTGGCCAGGATGGT[C/T]TTGATCTCCTGACCT | 5607 |
rs143703229 | snp | A/C | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547524 | GCAGTGGCGTGATCT[A/C]GGCTCACTGCAACCT | 5607 |
rs143704624 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589033 | TTTAGTTTGTAGAGA[C/T]GGGGTCTCACTGTGC | 5607 |
rs143715763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787245 | GCTGTTTCTCAAATT[C/T]TGCGAAGGTCTCTAG | 5607 |
rs143718221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705008 | GCCTCAGTTTCTTCA[C/T]TTGTAAAATATTGAT | 5607 |
rs143722898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599212 | ATTAGTAGTATAAAG[A/G]TAGTGATGAACAGAA | 5607 |
rs143724159 | in-del | -/TGTT | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676136 | CAGTGTGTGGATGAG[-/TGTT]TGATTCACCAAGCCC | 5607 |
rs143725012 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705858 | CAAAGGCACCAAGAT[A/G]GAGTACACTCTCAGC | 5607 |
rs143741263 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642381 | TTGCCCTTGAGAGGC[A/G]CATAGCCACTCTAAT | 5607 |
rs143749802 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571071 | GAGAGTCGTTACTAT[A/G]TCTATATCAGTTCCT | 5607 |
rs143751150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794969 | ACCTCTGACGCCCCC[A/G]CGGTGGGTGATGTTT | 5607 |
rs143763308 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650953 | GACAGGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 5607 |
rs143763417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710242 | TCTGCCTGTTTGCCA[C/T]CCCTCTAACCAGTCT | 5607 |
rs143764230 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652746 | TCTGCAGAACTCTTT[G/T]TGTCTTGCAAAACTG | 5607 |
rs143769330 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576957 | TTTTTGAGACGGAGT[C/G]TCGCTCTGTCGCCCA | 5607 |
rs143770471 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712685 | ACACTTTAGGAGGCC[A/G]AGGCAGGCGGATCAC | 5607 |
rs143785820 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807135 | TGCCATAAGAGTTGT[A/G]TGGTCCAGGGGGTCT | 5607 |
rs143801330 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659532 | TTCTTTTCTGATGCT[A/G]TTGCTCCTAAGTAGC | 5607 |
rs143807443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583928 | TTTTTTTTAATTTTT[C/T]AATAGCGACAAGGTA | 5607 |
rs143828938 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699914 | ATTCAAGCAGTCTAA[C/T]TCCAGAGCCCTGTTT | 5607 |
rs143872386 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763704 | TACAGATTTGCCCTA[G/T]GGGTTCTGCCAGTTG | 5607 |
rs143885101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707344 | ATGTTAGGAATAGAT[A/G]TAGCAAATCCAATTT | 5607 |
rs143894244 | in-del | -/T | 0.264632 | 0.249571 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643778 | GAAACCACCTATGCC[-/T]TTTTTTTCCCCACCT | 5607 |
rs143914560 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790937 | CCATATTTTACAGAA[A/G]ACGAGTCAGAGCTAG | 5607 |
rs143925949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794194 | CACCACCATCAAAAA[C/T]GCATTTCAGGCTTCT | 5607 |
rs143934097 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582014 | GAAAAAAAGAAATGT[C/T]GCTATTTCTGTTTAT | 5607 |
rs143944401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550652 | CAGAGGACATCATGG[A/G]ATGAGTCATGCTACG | 5607 |
rs143951594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747166 | TTTCCCATCATAGAA[G/T]AAAGATGATCATCCC | 5607 |
rs143960237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658448 | ACATCCAATGCATGC[C/T]GTAGGAAGTGTAAAA | 5607 |
rs143962299 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626202 | ACTTGGATTTACGTG[G/T]AATAAACTTACTAAT | 5607 |
rs143964797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772098 | ACAAATTTAGCTGTC[C/T]CACAGCGGTTTAATG | 5607 |
rs144005612 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582772 | GCTACAGTGAGCCAT[A/G]TTTGTGCCACTGTAC | 5607 |
rs144008829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635163 | CCCAAAATGCATTGT[C/T]ACTACTTTTGCTTTA | 5607 |
rs144012854 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562176 | TACGTTGCTCCAGAC[A/G]TTTTTGGCATTTCTT | 5607 |
rs144034315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696503 | CCAGTGAAAGTTGTA[C/T]CTGAAACTGAGCACC | 5607 |
rs144040989 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578742 | GACCTAAAATGAAAG[G/T]AAAACCATTTTTATT | 5607 |
rs144041631 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622296 | GTGGCCCAGCCCTCA[A/G]GAGTAGGTGCAAAGG | 5607 |
rs144041990 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709705 | CCATTTATATTCTTG[G/T]GTCATTTGAGTTCAC | 5607 |
rs144063192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583829 | TGTGCTCACTGCAGC[C/T]TTTATGTCCCCAGGC | 5607 |
rs144069789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766788 | TCCTTTGCTTTCCTT[C/T]GGAGTGTTAACAGCT | 5607 |
rs144071627 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774214 | GTGTGAGAGAACATA[C/G]GTATTTAGATATATC | 5607 |
rs144077569 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633994 | CACCCTTCCTATAAC[G/T]TAAATTGTTTTAAAT | 5607 |
rs144086053 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687753 | GTTAGTTCACCTGTT[G/T]AGTAGAGACACCATT | 5607 |
rs144087544 | snp | C/T | 0.296619 | 0.245615 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567457 | GCAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 5607 |
rs144097823 | snp | C/T | 0.031825 | 0.122064 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636268 | AAAAAATTAGCTGGC[C/T]GTGGTGTCGGGCGCT | 5607 |
rs144101603 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600726 | GGACACTCTTGGTCA[C/T]GGCAACGGAGGCACA | 5607 |
rs144115359 | in-del | -/TT | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546029 | CAGGTGTCTGCACAC[-/TT]TTGGCTAGGTAAGCC | 5607 |
rs144127068 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630521 | TATAGAGAACCCACA[A/T]GCACAGTGACAGTCA | 5607 |
rs144131275 | snp | A/G | 0.046775 | 0.145601 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556753 | AGACAGGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 5607 |
rs144136927 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689932 | CAACCCATGCTCCAC[A/G]GGCCACATGAGCCAC | 5607 |
rs144153034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737317 | TATACTCCAGTGTTT[C/T]ACTTATCACCATTCA | 5607 |
rs144157829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769208 | AAAGTGTAAATAAAT[A/G]GCAAATCCAGTAAAA | 5607 |
rs144202706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651718 | GCTGAATAATATTTC[A/C]TTGTGTTTATGTACC | 5607 |
rs144204660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605666 | CTATACAGCATTTCT[G/T]TTCTTTTTGCTTGGT | 5607 |
rs144216776 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652127 | TAGTGATGTCAAACA[-/T]TTTTTTCAAATGCCT | 5607 |
rs144228937 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732107 | TTTTAAATATCTTGC[A/G]AACAGTTTCTCAATT | 5607 |
rs144252350 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687994 | AGTATCTGAGCTGGG[A/G]GGTATTGCTACTGCA | 5607 |
rs144255324 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599012 | CCCACCAATGGATAC[A/T]GCTATTTACGTTTCC | 5607 |
rs144292781 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558521 | CAGGTGACACCACCA[C/T]GCTCACAACCCTCCA | 5607 |
rs144313598 | in-del | -/AC | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630489 | AAAATGGCTCTGTAC[-/AC]TGCTTAACATAGAGC | 5607 |
rs144333186 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563715 | TTCAACTGGAGATCT[C/G]TCTCACCCTTCCAGA | 5607 |
rs144353614 | snp | A/G | 0.0345262 | 0.126772 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703850 | TTTAAAAGATACAGC[A/G]CTACTCATTTAGATA | 5607 |
rs144354941 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683208 | ATAAGTTCAGTGGCT[A/G]TATACTAGGATTGTT | 5607 |
rs144375117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614833 | AATGTAGAGTTACAG[C/T]AGCTTTCTCTTATTG | 5607 |
rs144376618 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800437 | TGGCAATCTCATACC[C/T]ACACACAGCTTATTT | 5607 |
rs144378363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557375 | TGGTTTCACTTTTCT[A/G]TTACACTCATGTATT | 5607 |
rs144413112 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619147 | CCTCTACCTGGAATC[C/G]CCTTCCCCTAGATGT | 5607 |
rs144439366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801462 | TGAGGCAGAGCAGTC[C/T]TGTGGTCCAGAGAGC | 5607 |
rs144439715 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651723 | ATAATATTTCATTGT[C/G]TTTATGTACCACATT | 5607 |
rs144444691 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707041 | CTGCCTCAGCCTCCC[A/C/G]AGTAGCTGGGACTAC | 5607 |
rs144483371 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590514 | CTCATTGCTGTCACC[A/C]CCCCATTCTGGAGTG | 5607 |
rs144499909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789272 | ATAGGATATTTTGAC[C/T]ATTTCCATATTTTTT | 5607 |
rs144522875 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645894 | TTGAGGGTCATTCCT[A/G]TGCTCCTCTTTTGAA | 5607 |
rs144591944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627199 | AGTGATCCTCCTGCG[C/T]TGGCTTCCCAAAGTG | 5607 |
rs144594645 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586668 | AATAGAATATTATGT[A/C]ATGTATGGGTTATAC | 5607 |
rs144603842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803082 | GAGATGCATAGCTGT[A/G]TGTGGGCCACAGTGA | 5607 |
rs144621464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783200 | GGCAGCATGTCAGCC[C/T]CAAGTCCTGACCCCC | 5607 |
rs144623762 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805331 | CTGTCCCCCACAGTT[C/G]TGACCTGTGGTCCAG | 5607 |
rs144627181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675634 | TATTTCTTACCATTG[C/T]AAATGTAAACTTTGA | 5607 |
rs144629946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590365 | TCTTGAGTCCTTTCT[C/T]TTTTTTTCCTTTTCA | 5607 |
rs144630393 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587917 | GTCTTTCTACTCGCC[A/C/G]GCATCCCTGCTGCTG | 5607 |
rs144677100 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773115 | TCTGCAGAAAATTTC[A/T]GAATATGGCATGGAG | 5607 |
rs144701907 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635392 | ATGTTAGGCAGGATG[A/G]TCTCGAACTCCTGAC | 5607 |
rs144705301 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562697 | AGCTGCTTTACAAGT[C/T]AACCTTGCACTAGGC | 5607 |
rs144739765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764287 | AGGGAACAGGACCCA[G/T]ACTACAACATTCAAG | 5607 |
rs144745186 | snp | C/T | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548487 | TAATATGGCACTTGC[C/T]ATGTGCTAGACACTC | 5607 |
rs144745221 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597674 | AAAAAAGCAGAAATA[C/T]TACTGGTTGATTGTA | 5607 |
rs144783985 | snp | A/C | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553465 | AAACATACCCACAGA[A/C]AAAATAATGACAGTT | 5607 |
rs144806957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630353 | ATTTATATTTATTGA[C/T]TTAAGTTGTAGTTAT | 5607 |
rs144846295 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551065 | GTGTGAGCCACTGCA[A/C]CTGGCCAGAGGGTCA | 5607 |
rs144852172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781398 | ACCTTTGGGGATTGT[A/G]AGTCTTGTGGTTTCG | 5607 |
rs144854139 | in-del | -/T | 0.295854 | 0.245759 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571600 | CAAGATTTTTTTTTT[-/T]CAAGTACTTTTTAAG | 5607 |
rs144861618 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680365 | TATATTTCTTTAGAT[A/G]TTTGTAAATCATAGT | 5607 |
rs144882434 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733470 | AGAATGGCATTCAAA[G/T]AAATTATTGCAGTAT | 5607 |
rs144896265 | snp | G/T | 4.94262e-05 | 0.00497098 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543355 | TGTGGCTAGCCCTTG[G/T]CCCCTTTCCTGCCAT | 5607 |
rs144911138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601121 | AGTTATGCCCAGTGG[A/G]AGCCAGACCTTATAA | 5607 |
rs144922746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591205 | CAAAAATTAGCCAGG[C/T]GTGATGGCATGCACC | 5607 |
rs144977382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782177 | TGTTCCTTTCACAAA[A/G]AGGCAGTGTCTCCCG | 5607 |
rs144988486 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780584 | AGAAACTAATCCAAG[A/G]ACAAGCAATCCCTGG | 5607 |
rs144993021 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697270 | ATAATAATAGCTTAC[A/G]CTTAGGTAGCTTTAT | 5607 |
rs145026945 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704725 | GTCTCCCAACAGAAT[C/G]CACAAGGGCTTATTC | 5607 |
rs145031773 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640497 | CCTCAGCTGTGAAAC[A/G]GGGCTGCCTGATGTC | 5607 |
rs145033678 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702782 | GAATGAAATGTTGAA[C/T]AGCAGATGAATCTGG | 5607 |
rs145035591 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568734 | TCTGTTGGCTGGGCG[C/T]GGTGGCTCACTCCTG | 5607 |
rs145062114 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689989 | GCGCAAATTTGTAAA[C/G]TTTGTTAAAACATTA | 5607 |
rs145063072 | snp | C/G | 8.23771e-05 | 0.0064173 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585894 | TACTGTTTCAGCCTG[C/G]AAGCCTCCTGGGGAA | 5607 |
rs145066900 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762566 | TTTTAAATGACAGAC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs145093378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579997 | TCGAGCATTATAAGA[C/T]GTGAGAGCACAGAAG | 5607 |
rs145116345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559859 | GTCAGATGGCAAAGA[A/C]CCTCCATGTATAAGA | 5607 |
rs145150756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649262 | ATTGTTGAGTTGTGA[G/T]AATTCTTTATGTATT | 5607 |
rs145157968 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574816 | ATGTTGCACTGAGCC[A/G]AGATCGTACCGCTGC | 5607 |
rs145229568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722180 | TCTGTTACTCGCACT[C/T]ATGCCCCTCCACAGG | 5607 |
rs145231970 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762182 | CATTGGGAGGCTGCA[C/G]AGAAAGAGGACAATA | 5607 |
rs145251929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708768 | CCACACTCTTTCATA[A/G]AAGATGATGCTACAT | 5607 |
rs145268078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759965 | TATTGTCAACTAGAC[C/G]TGTGTTTCAAAGTGT | 5607 |
rs145276480 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765821 | TACCTTGCTGACAAG[C/T]GCTAATAACAAAATA | 5607 |
rs145284728 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686985 | TTTAAAGTTTTTAAA[C/T]TTTAAACACAGCAAA | 5607 |
rs145293053 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792448 | TCAAGAAAACCAGAA[C/G]TGACAAGTTCATTTA | 5607 |
rs145293604 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647614 | AATATGGCCGGGCAC[A/G]GTGGCTTACTCCTGT | 5607 |
rs145294578 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572985 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCTGATA | 5607 |
rs145296215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625795 | AACCCAAACTTCCAC[A/G]GATGAATTAGCGTGC | 5607 |
rs145312478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803471 | AAGGGCGTCAGTTAC[A/C]GTCTAGGAGGAAGGA | 5607 |
rs145323551 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759517 | GTGAGCCAAGATCAC[A/G]CTACTGCACTCTAGC | 5607 |
rs145323958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738012 | GTGCATCACCATACC[C/T]GGCTAATTTTTGTAT | 5607 |
rs145330801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678703 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 5607 |
rs145339143 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648874 | GTGAGCCACTGCACC[C/T]GGTCAGTGTTTTCAG | 5607 |
rs145352600 | snp | A/G/T | 0.0142791 | 0.083329 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805701 | TCTGTCCTCGCTATG[A/G/T]CTCCCCGAGTCTCAC | 5607 |
rs145362235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546782 | ATCTATAAGACTTCT[A/G]GGCCAGGAGTGGTGG | 5607 |
rs145366027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606957 | ACCAACCAACCTGAA[A/G]GTGTGAAACTTAAAG | 5607 |
rs145417766 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667610 | AAGTACCTGTGTTGT[C/T]CTCTGATCATCATTT | 5607 |
rs145418073 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780528 | CAGATAGACAAACAA[-/G]GACATGTATCTGGTT | 5607 |
rs145420081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587828 | AGTCCTCCTTCACTG[C/T]TTCCTAGGCCTCCCT | 5607 |
rs145429093 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784423 | AGGATTTCAGCAGAG[G/T]GTGCTTGTGAAGCCA | 5607 |
rs145439440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578552 | TGGATTTAGAGGAAA[C/T]ATAAAAAACAAAAAA | 5607 |
rs145447804 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774802 | CAGTTTATCTCCCAA[G/T]CATGGTAACTCCAGC | 5607 |
rs145455659 | snp | A/G | 0.000299451 | 0.0122326 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693480 | TTTTATTTCCACATT[A/G]TCTTTATATTGTTCT | 5607 |
rs145461029 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804857 | CCTCTGTCTAGGCAG[C/T]GATTTGGGAAAGCAG | 5607 |
rs145464809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754394 | CCACATTCCATTTCG[C/T]AGAAGACTACCACAG | 5607 |
rs145551957 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554357 | AGCCACCGCACCTGG[A/C]CTTATAGTAATACAT | 5607 |
rs145554592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768690 | AGATGAGAATGGAGT[C/T]ATTTGCAGCTGCCTA | 5607 |
rs145578631 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632871 | CATATCACATCTAGT[A/T]CAGCACCTAGAATGT | 5607 |
rs145593249 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558786 | GTCTTTCCCCAGATA[A/G/T]CAGCAAGGCCCACTC | 5607 |
rs145617367 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650328 | TTCCTTTTCTTGCTT[A/T]ATTACCCTGGCTAGA | 5607 |
rs145630692 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734387 | TTTTTTTCAATTGAC[-/A]AGACTGTCTTTTAAA | 5607 |
rs145636235 | snp | A/G | | | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67693565 | AACAAATGCTTATAT[A/G]GCGGTAAGTAAACTT | 5607 |
rs145650864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627035 | CTCCTGGACTCAAGC[A/G]ACCCTCTTGCCTCAG | 5607 |
rs145655393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743745 | AGCACAGTGCCAGAT[A/G]AAATTAGATTGATTG | 5607 |
rs145657343 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552052 | CCCTGTAAAGTGGAC[A/T]TGGGGCCTGAGGCTT | 5607 |
rs145671127 | in-del | -/TTTA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583752 | TGTTTCCTTATTTAT[-/TTTA]TTATTTATTTATTTA | 5607 |
rs145713323 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785880 | GGATGTCAGAAAATA[C/T]AGCTTCAAGTACAGG | 5607 |
rs145738962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601411 | TACATAATGTAATAT[C/G]TGGTACTTAATAGTC | 5607 |
rs145747663 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764404 | TTTACTTTATGCCCC[A/G]TGACCCTCGTTTGTG | 5607 |
rs145783301 | snp | A/C | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 15:67750518 | GATGCAGTGTTCCTC[A/C]TAGGGTGGACCAAGG | 5607 |
rs145788635 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584059 | TGGCCATAATTCTGA[G/T]GTAATAACATGTTCT | 5607 |
rs145808145 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574084 | ATTCTTTCTGGCACG[A/G]CATCCAAGAACCATC | 5607 |
rs145809931 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699522 | GACCATAGCCTAGCC[A/C]TAGTATAGATTTACA | 5607 |
rs145812318 | in-del | -/AAAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711629 | AACCTCCACTAAAAA[-/AAAAT]TAGCCATAACGTGAT | 5607 |
rs145855898 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598137 | TTGAACTTGAGATGT[A/G]GAGTTTGCAGTGAGC | 5607 |
rs145866877 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712782 | AATTAGCTGGGTGTG[A/G]TGGCAGGTGTCTGTA | 5607 |
rs145872700 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623552 | AGTCTGTTTTGGCAG[C/G]TTTCATTCTGAAATC | 5607 |
rs145888802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733949 | TATGAGAGGAGCTGT[A/G]GGTGGCATTTGCTTC | 5607 |
rs145927000 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587158 | CGTTTCAGACGGAGG[A/G]AAGAGGGTAGGTGAA | 5607 |
rs145928390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797254 | TGGCTTTATATATAG[C/T]TACTGCTTGTTCAGA | 5607 |
rs145975824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583860 | TGGAGCAGTTCTCTC[A/G]CCTCAGCTCCTGAGT | 5607 |
rs145998126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778778 | CCAAAGATAAGTTTC[A/G]GTTTACTTTGATCCG | 5607 |
rs146009683 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732259 | GCAATGGTTTGTTTA[A/G]TGACACCATAATTTA | 5607 |
rs146025371 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544537 | CAGAACTAAAATTTT[G/T]TTTCATTGACTTAGT | 5607 |
rs146032543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663188 | CTTACATAATCACTG[A/G]TTAAAATCAGGAAAC | 5607 |
rs146033282 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774245 | TCTTTACAACTCTAT[A/G]CCCTGTTGTGTGCTG | 5607 |
rs146045367 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638586 | CATTTGGGTATATAC[C/T]CAGTAATGGGATTGC | 5607 |
rs146050016 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567229 | TGCATTTTGTTATGA[A/G]TTTGTGTTAATCAAC | 5607 |
rs146061242 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572150 | GTTAGGACAAGGGGA[C/G]TAGGAAGGATGTTTG | 5607 |
rs146085596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563880 | GAATATATTCTGAAA[C/T]GACTTTTCTTTTGTG | 5607 |
rs146092530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778394 | CAGTGTGACTTTGGG[C/T]TTCACACCAAATGGC | 5607 |
rs146095610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635798 | TGTTTCACTGTTTTC[C/T]TTCTTTCCAGTGAGA | 5607 |
rs146095626 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695344 | TTCTTCTCAGAACAA[C/T]ACAAAACATTTTGTT | 5607 |
rs146122590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758684 | GAGATACTTAGCTAA[C/T]AGATATGGTTCTCTA | 5607 |
rs146133946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712485 | GCCAGAAAACTGTGC[A/G]GAGGGTAAAAAGTTC | 5607 |
rs146168977 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793244 | CTTGTGAATAGCCAC[C/T]GTGCTCCAGTCAGGG | 5607 |
rs146171688 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621962 | GCCAAGGTGGGTGGA[C/T]CACCTGAGATCAGGA | 5607 |
rs146172002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545109 | AGGTGTCCAGGCTGT[C/T]TGCACTCTGCTCTTC | 5607 |
rs146184165 | snp | C/T | 0.00161335 | 0.0283562 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550089 | CATTTGAATGTAAGT[C/T]TGGCTTGTATACTTT | 5607 |
rs146208573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710275 | TGAGTCTGAGGCATA[A/G]AACAGTCTGGCTCAA | 5607 |
rs146215066 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758213 | TCAGAAATTGGAGGG[G/T]TTTAATCAGGACAGC | 5607 |
rs146220733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675993 | CCAGTCCCCACCTCT[A/G]AAAGCCTTCTGACTT | 5607 |
rs146221055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618887 | TCCTTGCTTTCCTGT[A/G]ATGTGTTCTCTTCAC | 5607 |
rs146250666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692285 | CCAGAAATCGTTGAA[C/T]GTGGAGGAGTTAAGA | 5607 |
rs146291016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604413 | AAAGACACATGTTCT[A/G]TTTCCCTCTGAGAGA | 5607 |
rs146320185 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585001 | GCACCCAGTCATTAC[C/G]CACATCTTATTATTA | 5607 |
rs146338809 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599558 | GGTGGAAGTTTAGAG[G/T]AGAGCAAAATATTTA | 5607 |
rs146339160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644506 | ATATGTGTTTGAAAT[A/T]AACTAGAATTTATTC | 5607 |
rs146358278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799824 | GAAGCCAGGAGAAGG[A/G]AGGCCCCCTCCACTC | 5607 |
rs146374999 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666050 | TTAAAAAATGGACAT[A/C]TATCCATTTGACAAA | 5607 |
rs146406078 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795074 | TCTGCTGTTGTGAGT[C/T]GTCACTCTCAGCATT | 5607 |
rs146418531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765990 | GGCAAAGGCATCACT[C/G]AAACTTTTTCCTATT | 5607 |
rs146484861 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727636 | TAAATGTGAATAATG[C/G]CCATATAGCTGAGAA | 5607 |
rs146485042 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592641 | TAAAGGCAGTAGAAC[C/T]AATGACCATAAAAAT | 5607 |
rs146509083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769992 | CTACTGAACGGACGT[A/G]CGAAGCTTATTTTTA | 5607 |
rs146519211 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634044 | GGCTCAGAATATGAC[C/T]TATTTTGGTAAACAG | 5607 |
rs146543019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743943 | TCCCAGGGGTCTTTC[C/T]TACTCCAAAGTTCAT | 5607 |
rs146593607 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619256 | TCAAATAGCATGTCC[C/T]TAATGTTGATCAGTC | 5607 |
rs146606163 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707075 | CGCGTGCCACCATGC[C/G]CGGATAATTTTTTGT | 5607 |
rs146618934 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578923 | TTAGACATCTCTATA[A/G]TTAACTTGTTAGATA | 5607 |
rs146638833 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703953 | TGTGGGTTAAGGGGT[A/G]GTGTGATATGATGGA | 5607 |
rs146725736 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689062 | TTGGTGATGATACTG[A/C]TAACAGCAAAAACAT | 5607 |
rs146739378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558599 | CCTCCAAGGCTCTGC[A/G]TTTTCGCATCTGGCC | 5607 |
rs146749811 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725396 | GCTGTATCTCACTCC[A/G/T]TTTTAAGCCGTCCAT | 5607 |
rs146749845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775984 | CCTGGGAACACCACA[C/T]TTATCCACATGGATC | 5607 |
rs146760004 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686707 | AATGACAAAACCACT[C/T]AGTGATTTACCAAAG | 5607 |
rs146761382 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597774 | CTAAAAATATTTTTT[A/G]TAATCAATTCTTGGG | 5607 |
rs146781510 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785368 | TTGTGAGCGAAGAAA[G/T]CTGTTTGCGGTTCAC | 5607 |
rs146831751 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729509 | GGTGCAGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 5607 |
rs146841009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748176 | CAGTGATCATAATGT[A/G]TCCAAGTGAGTCATT | 5607 |
rs146846275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610508 | CACAAGCAAATATTT[C/G]TGTACCATAGCATCT | 5607 |
rs146846394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660295 | TAGTGTTTTTTTTGT[A/G]TGTTTCCTGAGTAGG | 5607 |
rs146858171 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614736 | AAGAAATATGGAGGT[A/G]GTGATGACCACATTA | 5607 |
rs146869178 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791351 | CTTTGTTATGCAGGG[A/G]CTTGTTTTGACCACT | 5607 |
rs146870676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637833 | CTGGGCAATCATAGG[A/G]CTCATCTCATTTGTT | 5607 |
rs146880570 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743371 | GAACTTGAGCAAGGA[C/T]AGAGGCTGATGAACA | 5607 |
rs146881409 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653979 | CTGTTTAATTTCCAC[A/G/T]TATGCGTACTTGAGA | 5607 |
rs146888784 | in-del | -/GA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774202 | TGTGTGTGTGTGTGT[-/GA]GAGAGAACATAGGTA | 5607 |
rs146905808 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772233 | TACTTCTTGTCATTC[A/C/G]GAGTAACAGTGAAAG | 5607 |
rs146952830 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561742 | ATTGCTGTTGGCCAC[A/T]GAAGAGATAAAGGGA | 5607 |
rs146972195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755850 | AAGTCTGTTTCCATC[G/T]TAAGCAAATCCACTT | 5607 |
rs146991333 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701794 | TGCGATGGCTGCTCC[-/A]AAAACTGCACATTGA | 5607 |
rs146995518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709691 | ACTAAGTAATTATTC[C/T]ATTTATATTCTTGTG | 5607 |
rs146995706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621315 | GTTTATATACACACC[C/T]TAGTAAAGAATAACT | 5607 |
rs147008354 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657721 | ATAAAGCCAGTAGCC[-/AT]ATATATATATATATA | 5607 |
rs147027127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620911 | AAGAGAAGTCGATAG[A/G]TGTAAAGTAAATGAA | 5607 |
rs147056341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671396 | CAAAGTGGGAAATTC[C/T]AGGAAATATGAAATG | 5607 |
rs147069934 | snp | G/T | 1.65466e-05 | 0.00287628 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543296 | AACCAGCGGCCAGTG[G/T]GTTTCCCATACCCCA | 5607 |
rs147077662 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734145 | ACTTTCATTTAAAAC[C/T]GATTAATTTATTTGC | 5607 |
rs147098845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690564 | TTTTGAGACAAGTCT[C/T]GCTCTGATACCCAGG | 5607 |
rs147100192 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603134 | GTATAGTTAGTGGCA[G/T]TAAGTACATTCACAT | 5607 |
rs147119925 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730360 | GTGAAATAGCCTCCC[C/T]TCATAAATTGGACAA | 5607 |
rs147134458 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783395 | TCCCCAGATGCGTGA[C/G]GCATCCTCACACAGT | 5607 |
rs147146805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706157 | ATATATTTATGTTGC[A/G]TATTGAAATATGTGT | 5607 |
rs147171817 | snp | A/G | 4.94694e-05 | 0.00497316 | missense, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703405 | AGGAATCTCTTTTAT[A/G]GAGGTACGTTGTTTG | 5607 |
rs147179682 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656519 | TTTTTGGTAGAGATG[A/G]GGTTTTGCCGTGTCT | 5607 |
rs147207553 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677148 | TGTGAACTTCCCAAG[-/A]TCACCCAACTATTCA | 5607 |
rs147213639 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577325 | TCCTGAAGGCTACAC[A/T]AGTTAATGAGTGGCA | 5607 |
rs147223902 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756807 | GTTTCTGTGTCTGAC[-/T]TACTTCACTTAGCAT | 5607 |
rs147225336 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651116 | CCAGCTACTTGAGAG[G/T]CTGAGGCAGGAGAAT | 5607 |
rs147231946 | snp | A/C | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547077 | CTCAAAAAAGAAGAA[A/C]ACACACACACACACA | 5607 |
rs147244234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763943 | CCAGGGCAAAGGAAC[A/G]TCAGACATGAATTAA | 5607 |
rs147244737 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685020 | GAAGAGGAAAGAGAA[A/G]AGGAAACAAAAAATA | 5607 |
rs147274723 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807259 | TCCTGCTAGCTCCTC[A/G]CAGTTGTGCTGAGGC | 5607 |
rs147312395 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595749 | AAAAATAAATCAGAA[G/T]ATATTTTTGGCAAGT | 5607 |
rs147317264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767214 | ATGTCACATTTCCTC[A/G]TTTTGTTTCTCATCC | 5607 |
rs147332104 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630678 | ATGTATCAGTATTAC[C/G]TCAGATAGTTATTTT | 5607 |
rs147333373 | in-del | -/ATGTGAAGAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592807 | TACATTGGGAGAAGG[-/ATGTGAAGAA]TATGCTCAATCCCTA | 5607 |
rs147356790 | in-del | -/ATC/ATT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612063 | CTCCCTGGAAATTTT[-/ATC/ATT]ATCTTTGGTTTTCTT | 5607 |
rs147360998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745802 | GATGTTGCATCATCA[A/G]ATTCTTGTGAAATAG | 5607 |
rs147393641 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705597 | AACAATTAGCTGGGT[G/T]TGGTGGTGTACACCT | 5607 |
rs147393936 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617887 | TTGTTGAGATGAGGT[A/C]TCATCTATGTTGCCC | 5607 |
rs147416771 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576416 | AAAACAAAGCAAAAA[A/C]TTGTACTTGTTATCC | 5607 |
rs147435626 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702373 | GACAATAATGTTATT[C/T]CTGTAGCCGGCTAGC | 5607 |
rs147436967 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613219 | AGCCATCTTCCAGAA[C/G]AGTAAGGCAAGAACA | 5607 |
rs147441072 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658660 | TGAGTGATTTAATCC[G/T]TCTAATCAAGCTCAT | 5607 |
rs147451047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804785 | AGAAGGGCACGAGGT[C/T]GCCCCTCCTGAGCCT | 5607 |
rs147456996 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721361 | GGACAAGTAGTTGTT[A/G]TTTTTTGTTTTGGTT | 5607 |
rs147466493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725660 | AAGCTATTAGCTTTT[C/T]TAGGTGTGAGACTCT | 5607 |
rs147497075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687673 | TCATTCTGAACTGTA[A/G]TCCATTAAATGGGAA | 5607 |
rs147498513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598827 | AACCTTAGTGCCACA[A/G]ATGCAGAATTTGTGT | 5607 |
rs147522367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555430 | CCAGGCCCCGCCTGC[A/G]ACATTGGGGATCACT | 5607 |
rs147526632 | snp | C/T | 0.0002609 | 0.0114185 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806882 | CCCTCGCCTTCACCT[C/T]TGTCAGCAGGTGGCC | 5607 |
rs147530901 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596354 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCAAGACTG | 5607 |
rs147562231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640700 | TTGCTTTTCCTACTC[A/C]AAATGTTTCTCATGT | 5607 |
rs147571884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647661 | GAGGCCGAGGCAAGC[A/G]GAGTTTGAGACCAGC | 5607 |
rs147572517 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572986 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCTGATAT | 5607 |
rs147576988 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775610 | AATCTTTTGGAGCTA[C/T]AGCAAGTATACAAAT | 5607 |
rs147591599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697339 | CCTCACAACACTATG[A/G]CATAGGTAATATTAT | 5607 |
rs147599995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780648 | ACGCTAGAATACATG[A/G]CCAGATAAAAAAGGT | 5607 |
rs147617965 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767479 | ACACCCTCAAAAAAA[-/A]TCCATGAAGCGATGA | 5607 |
rs147666421 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624200 | AAATATTAGCCAGGC[A/G]TGCTGGCGGGTACCT | 5607 |
rs147676655 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627095 | AGAGGACTACAGGCA[C/T]GCACCACGATGCCAG | 5607 |
rs147686017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755409 | CAGAAATATTAGCTG[C/T]CCCTTAGTCTGCCTG | 5607 |
rs147686170 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804928 | AGCCAAAATCCAGTC[C/T]TTCCTGGGCCTCTCC | 5607 |
rs147695267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759531 | CGCTACTGCACTCTA[G/T]CCTGGATGACAGAGC | 5607 |
rs147695964 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680002 | GTCCTCAGCCCCAGG[G/T]AACCACTGATTTACT | 5607 |
rs147780477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565292 | TGGAGTGCAGTGGTG[C/T]CATCTTGGCTCACTG | 5607 |
rs147790785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733978 | TCAGAACCTCCTGCT[A/G]TTAACCAAGGAAATA | 5607 |
rs147800462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737371 | GGGGATAGGGGCTCA[C/T]TGGCTTCCAAGTTAA | 5607 |
rs147801408 | in-del | -/TATT | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687340 | GCCAAGCTTAGGAGC[-/TATT]TATTTGCATAACTTT | 5607 |
rs147819337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801927 | ATAGGTACATTCCTA[C/T]TTCAGAAGAAGCTCA | 5607 |
rs147855939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568032 | ATCCTGTGTCTAGGG[A/G]TTTATTACACCTGGT | 5607 |
rs147865068 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588192 | CAGCTTGCTGGCCCA[C/T]CTCTGTACCCCATCC | 5607 |
rs147873707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669762 | TGCTAAAAATACTTC[C/T]TGCTACTTTCTTTCC | 5607 |
rs147883714 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678587 | TAGGTCACAACAAAA[A/C]GGGAATCCTCAATTG | 5607 |
rs147887842 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591517 | TGGGACTACAGGCGC[C/T]GGCCACCACACCCGG | 5607 |
rs147888194 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543179 | GCGGGTGCGTTCCTG[A/T]TCACCCCTCCCCTCT | 5607 |
rs147903506 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662509 | TGTTCAGTGTATCTG[C/G]TGTCTAATTATGAAT | 5607 |
rs147906608 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718750 | GCTTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 5607 |
rs147913817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801269 | ATGTGGAGGTCCCTT[C/T]GGCCTCTCAAATCAC | 5607 |
rs147926074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781515 | GACATTTGGGCCTAC[C/T]GTCCTCTATTTAATT | 5607 |
rs147938215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642102 | ACGAATTAGAGTACA[A/G]CAGATTAGCTCCACA | 5607 |
rs147951359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545771 | AAAAGTTGGGGAGGG[A/G]TGAAAGTAATGCCTA | 5607 |
rs147976689 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687122 | TGATTTTTTTAATGA[A/G]ATTTATTTCAAAAAG | 5607 |
rs147981378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597929 | CACAGTCAGGCCGGG[C/T]GTGGTCGCTCATGCT | 5607 |
rs147990870 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554398 | AAATATACCTAACAC[C/T]AATTGATATCTTATA | 5607 |
rs148037370 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753671 | AGGATGGCTGTAATT[-/A]AAAAAAAAAGAAAAG | 5607 |
rs148038436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792821 | AACTTGGGCCCAAAG[C/T]GGCCCCGTATGTCTT | 5607 |
rs148042858 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548416 | TTTCAAAGTTTATTA[C/T]GAAGTAAGCTTTGTA | 5607 |
rs148051396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664522 | AAAAAAAAATGTTGA[A/C]TGTATTTAAATATGG | 5607 |
rs148087821 | in-del | -/TTACTC | 0.420415 | 0.182917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580532 | TCTTAATCAACACTT[-/TTACTC]TTAAAGATAAATGCC | 5607 |
rs148094580 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634410 | AAAAAAAAAAAAAAA[A/G]AATGTATAATCCACT | 5607 |
rs148103278 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786563 | CCAAGCTGCTGGCTT[A/G]GGTGGTGCGGGAGCT | 5607 |
rs148114776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650570 | TCAAATGCCTGTTTT[A/G]TATCTATTGAAATAA | 5607 |
rs148115377 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575405 | GAGTGGTTGTTGCCA[A/G]AGAAAGAGCCAGAGG | 5607 |
rs148121193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773257 | TCTCAGCTCCAAGGC[A/T]GCTTTCTTTGATTGC | 5607 |
rs148135397 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720957 | GCTTTTCAGCATTCA[C/T]GGTTAGGCTATAGCA | 5607 |
rs148137560 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603303 | TTAATTAGGGCTACT[A/G]TGTCAAAGGGACCAT | 5607 |
rs148154004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782072 | TCTGAATCCCCAGTG[C/G]AGCAGCAGTCATTGT | 5607 |
rs148177848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734351 | AACTTGGCTTGGAAA[C/T]GTGCTATTTTAATGT | 5607 |
rs148181457 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560664 | CCACTTAAGCAAATG[C/T]TCTTGTAATGTTTCA | 5607 |
rs148198213 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757485 | CCTTTCCCACACACC[A/T]GCATAAAAGAACTGA | 5607 |
rs148261370 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710415 | CATGGCTTAGAAAAA[G/T]GTCTCAACATAGGTA | 5607 |
rs148276074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583087 | TCCTCCTGATAGTTC[A/T]GCCTATTAGGTATTA | 5607 |
rs148313175 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744413 | AAATAATACAAGCTT[A/G]AAAAGCAGTAAATAT | 5607 |
rs148318366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655687 | AATAATGTGTATAGA[C/T]GTAGATCTCTTTGAG | 5607 |
rs148327859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611672 | ACACAGATAAATGAA[C/T]GGATTTCCCTGAGGA | 5607 |
rs148344884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683439 | ATATAAGGTCAATAC[A/C]ATGAACAAAAGACAA | 5607 |
rs148350040 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776214 | CCCACCCCCACCCCC[A/C]CCTCCACTTCTGCCT | 5607 |
rs148354508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762884 | AATTCAGGCCTTTAC[C/T]CCGTGGTTCCAGGCC | 5607 |
rs148378812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607580 | GCAGAGATTTTCAGA[C/T]TCAGTTTCCACCCGA | 5607 |
rs148383401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806526 | CTGATAGCCTCCCTC[A/G]TTACCTCACAGGGTT | 5607 |
rs148426534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789806 | GTTTGTTGGTCACAT[G/T]TTTTTTTTCACATTC | 5607 |
rs148430059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578641 | GTGACTGTGTTAGTC[A/G]TAGTACAGAGAGATG | 5607 |
rs148432349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545145 | TCAATTCCCACCTGT[C/G]CTTCCAAGCCAAGTT | 5607 |
rs148439312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652029 | TTGCCAGCATCTATT[A/G]TTCCCTGTCTTTTTG | 5607 |
rs148451378 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605270 | ATGTTGGCCAGGATG[A/G]TCTGGATCTCCTGAC | 5607 |
rs148456127 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804974 | CCAAACCTCTGCCAT[C/T]CACAGGGCCACACCC | 5607 |
rs148479986 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783263 | GGTAGACACAGCCAA[A/G]CACAGGATAGAATGT | 5607 |
rs148489627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735714 | GAGCCGAGGCTCTGA[A/G]GCAAGAAGGATGGGA | 5607 |
rs148504473 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635471 | TGAGTCACCGTGCCC[A/G]GCCTGGAAATATTTA | 5607 |
rs148512433 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726657 | AGTTGCAAATCTTAG[C/G]GTCAGTTCCTAGGCT | 5607 |
rs148513612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759383 | TGGCAACATGGTGAG[A/G]CCCGATCTCTACAAA | 5607 |
rs148575031 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713046 | GAAGAAATCATCAAA[G/T]AAAAATTTTAAATTT | 5607 |
rs148575377 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623685 | TCATCGTAACCTCCA[C/T]CTCCTGGGTTCAAAT | 5607 |
rs148608198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573293 | AAGAGGTTTAATTGA[C/T]ACAGTTCTGCATGGC | 5607 |
rs148628338 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626480 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCACTC | 5607 |
rs148649692 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703523 | AGCATGTTATATAGA[C/T]GTATACAGAGTTTGA | 5607 |
rs148650802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614260 | CTCACAAATTTTTGT[A/G]GAAATCAAATAGCTT | 5607 |
rs148660818 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658899 | TCTTCTGAAAAAAAA[A/T]TGCTGTTTTTTGTTT | 5607 |
rs148665967 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764626 | ATGCCAGGCTCATTG[A/C/T]GTTCCACATGGTAGA | 5607 |
rs148697367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779336 | ATCGGCAGAATCACT[C/G]TCTGGATACTTGAGA | 5607 |
rs148711734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688247 | GGGCAGCTCACAAGG[A/G]CCTTGGGGACCTCTG | 5607 |
rs148712328 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599056 | GTAAACCAAACAGCA[A/G]CTCTGCTAGTTTAGC | 5607 |
rs148755837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732183 | TCTAGACAAGGACTG[A/G]AGCTGCCTATAGTTA | 5607 |
rs148776341 | in-del | -/TTCT | 0.0287284 | 0.116357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772442 | TTTAATTTAAATTCA[-/TTCT]TTATTTGTGTTGCAA | 5607 |
rs148778263 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551013 | CTGACCTCAAGTGAT[C/T]CACCCACCTCAGCCT | 5607 |
rs148783976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668349 | GTGATAATTCCACAT[A/G]AGGACATAATCATTA | 5607 |
rs148789163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558238 | GGCACGTAATAGGCA[A/C]TCTATGTGTGTTTCT | 5607 |
rs148795170 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753611 | CAACAATTAATTAAG[A/G]AAATGCAAATCAAAA | 5607 |
rs148829078 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728728 | AGGTGGTGTTGGTCT[C/G]TGCTCTTTAAGCATC | 5607 |
rs148858922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775371 | AGAAATTCCTTTACT[A/G]CTTACATTTTGGGGA | 5607 |
rs148882555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722228 | GTTATCAGCTAATGG[C/T]GTTATACATTAAAAA | 5607 |
rs148892947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597842 | ACATGAGGAGTATTT[A/G]TACAGCATATAAAAA | 5607 |
rs148931995 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776208 | TAGAACCCCACCCCC[A/C]CCCCCACCTCCACTT | 5607 |
rs148945161 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627650 | AAATCATTTCTATAA[A/G]TCAGTCACCTTCAAA | 5607 |
rs148945381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553257 | AGGTTCAAACACACA[C/T]CTTTTTGACTATAAA | 5607 |
rs148954499 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750559 | TCAGAATTACCTAAG[G/T]CTCTTGTTGTAATGC | 5607 |
rs148963475 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615845 | TTTTGTTTGTGTCAG[C/T]ATTTGTGTACTCATG | 5607 |
rs148972407 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781972 | TCATGGTGATTGACA[A/G]CATTTGATTATGACA | 5607 |
rs148976222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570516 | TAAGTAAATGTAGCT[A/G]TTAATTTGATATTCA | 5607 |
rs148984531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642323 | TGAGTTAGACCCTGT[A/G]TGGAGTGCTGGGGGG | 5607 |
rs149018380 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584120 | TAGTAACTCCCAGGT[C/G]ATGGCTAAGTCCTCT | 5607 |
rs149027564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601170 | GTGTCAACACTATAA[A/G]TTATTAAAAAGCCTT | 5607 |
rs149069038 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733741 | CTTGTCTCAAAGAGG[A/C]ATTCTTAAATCCCAA | 5607 |
rs149091893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685822 | AACCCATGGGCAAAA[A/G]TTGGGCCTTCGCCTG | 5607 |
rs149103209 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560112 | TTTAGGCTACTGTCA[C/T]AGTAATTTGCTTAGT | 5607 |
rs149110462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756675 | GTTTGTCCCCTTTGA[C/T]GAACACCTCCTCATT | 5607 |
rs149152302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680167 | AGTTCATTCCTTTTT[A/G]TTGTTGAATAGTATT | 5607 |
rs149164575 | in-del | -/GGG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743044 | AACTAATTTATGGCT[-/GGG]GTGATGATTTTCTGT | 5607 |
rs149174609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655471 | TTCTCCTTCAGTTTC[A/G]TAGAATAGTTTTTGC | 5607 |
rs149197373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607246 | GTATATGACTGGATT[G/T]CATTATAGTATCGTG | 5607 |
rs149212502 | in-del | -/C | 0.0228947 | 0.104514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654139 | TTGAAGTCTCAAAAA[-/C]TAATATTTTTGAGTT | 5607 |
rs149217484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784911 | TGAACTCGGAGTATG[A/G]GCTGTGCACCAGTGG | 5607 |
rs149227395 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738049 | TAGAGATGAGATTTC[A/G]CCATGTTGGCCAGGC | 5607 |
rs149228815 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619399 | GGGACTTGGTCTCAT[C/T]TGTTCTCTGCTGTAT | 5607 |
rs149238314 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706414 | TCAGCATTGAGTGTG[C/G]GACACCTGAATGCTG | 5607 |
rs149267707 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752141 | CACAACCTCCGCTCA[C/T]GGCAACCTCTGCCTT | 5607 |
rs149269993 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720784 | GAAAGCACATATGCT[C/G]CAGTCACAGCTAAAC | 5607 |
rs149270418 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630053 | GGCCAGCCTGAGCAA[C/T]ATCCAGAGACCCTGT | 5607 |
rs149285809 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783127 | ATTTCAGTCTGCACT[C/T]GCCATTTTTATGTCT | 5607 |
rs149290468 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702296 | CTAAAACAAGGCCTG[G/T]TGTATAGAAATTCTT | 5607 |
rs149300562 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645433 | CAGTGAACCAAGATC[G/T]CCCCACTGCACTCCA | 5607 |
rs149323515 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714489 | TGTTTCTAATGGGTG[C/T]GTGGTTGTGGCTTTG | 5607 |
rs149331257 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663940 | TTACACACAGAAGTA[C/T]AGAAAATTAAGAAAG | 5607 |
rs149335190 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586587 | TCTAGACAGTGAGTT[G/T]GATTTTCACACTGTT | 5607 |
rs149353654 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691925 | AATTTCTAAGTATTA[C/T]CTGAAGTAGCATTTG | 5607 |
rs149356018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574943 | AAGAGAAGAGAGATG[A/G]TTTGGATTACTTCCA | 5607 |
rs149362620 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804621 | TCCCTCCTGCAGTTC[C/T]GCTCTGCTTGTTCCA | 5607 |
rs149405705 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766601 | CAGTGAAACTGGAGC[A/G]CAAATTTACTGTATG | 5607 |
rs149417549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562527 | CACATTCTGGTTATG[C/T]AGTTTGTGAAGTCTT | 5607 |
rs149449482 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746447 | GTGGGGGGAGTATCA[A/G]TGTGTGCTTGAAAAA | 5607 |
rs149465022 | in-del | -/TG/TGTG/TGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637920 | GTTGATGTGTGTGTG[-/TG/TGTG/TGTGTG]AGTGTGTGTGTATGT | 5607 |
rs149472342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595143 | CATTAAAAGAAAGGG[A/G]CATGATTCTTCAAGA | 5607 |
rs149479856 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793882 | AGAGTCATGAATGTG[C/T]CAGGGAAAGTCCTTA | 5607 |
rs149480890 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682552 | TAAGAGCTGTAGGTT[A/G]GCTGGATGTGGTGGC | 5607 |
rs149495047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550377 | AGGACAAAATGAAAC[A/G]TGTAAACTACCTGTA | 5607 |
rs149503108 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741418 | GCTTCTTCCTTCACA[A/G]ACCAAGAATGGTTAT | 5607 |
rs149510664 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696208 | TTCTACATGAGCCCT[A/C/G]TGCCAAATATCCATG | 5607 |
rs149514847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609358 | ATAATCAAGACAATA[A/G]ACACTGAAGTAAGAT | 5607 |
rs149535782 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675521 | TTCTCCATCTTGACT[A/G]TCAGTGTCAATACCC | 5607 |
rs149537315 | in-del | -/CTC | 0.290718 | 0.246662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583971 | CAGGCTGGTGTCAAA[-/CTC]CTCCTGAGCTCAAGC | 5607 |
rs149546974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544058 | TGGCACATGCCATCA[C/T]ACCTGGATAATTTTT | 5607 |
rs149554914 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778007 | TTAAAATCAGAATAG[C/T]GCTCTTGGATTTTTT | 5607 |
rs149564885 | snp | C/G/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731843 | ACTCTGCCCCACAAC[C/G/T]CTTCTTCTAGTTTGC | 5607 |
rs149617736 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725188 | AATTTTCTCTCTGTT[A/G]TCTTGCATGGCATTG | 5607 |
rs149625170 | in-del | -/C | 0.200182 | 0.244986 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744837 | TTTTCTAATTGCTAA[-/C]TGATGGTCCTTGTAA | 5607 |
rs149625618 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806210 | AAGCTAAAAGGGATT[A/G]ACATAGCCTCTGACG | 5607 |
rs149639411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598913 | GTAGCTTGTTAGTTA[A/G]TAGTACAAATCAGGT | 5607 |
rs149671324 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577958 | TGGGCCAAGATTGTG[C/T]CACTGTACTCTAGCC | 5607 |
rs149678100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774801 | GCAGTTTATCTCCCA[A/G]GCATGGTAACTCCAG | 5607 |
rs149691155 | in-del | -/CCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569730 | ATAAGCACGAGTAGG[-/CCT]CAGTCTTGGTGGCAC | 5607 |
rs149692361 | in-del | -/GTGT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637928 | GTGTGTGAGTGTGTG[-/GTGT]TGTATGTGTGTTTTA | 5607 |
rs149731472 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768379 | AAGCTATTTCCTCTC[A/G]TTCTCAATAATGAAT | 5607 |
rs149742756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564754 | TCTCCTGAGAATGTG[A/G]CATGCTTATTTTTAG | 5607 |
rs149794654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685161 | CACATCAAAATAAAA[A/G]TTTTGATAACCAGTG | 5607 |
rs149795965 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597400 | TCCATACTTAATACC[A/G]GAGACAAACTGCTGA | 5607 |
rs149804924 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796509 | AGGTGCCACACACTT[C/T]TAAAGGATCAGATCT | 5607 |
rs149805369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552797 | GGAAATCTTTAAGCA[A/G]CTTGCTGAAAGTCTC | 5607 |
rs149811809 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743191 | AATACAGCACCCCAG[A/C]TGGAGTCTGAGATTT | 5607 |
rs149816941 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623328 | GGTAAGAAATCTAGA[A/G]GTTGGAACATGGTAT | 5607 |
rs149823125 | snp | A/G | 4.96397e-05 | 0.0049817 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67769634 | AGTTGGAGAGTTCTC[A/G]GAGCCATTTGTACAT | 5607 |
rs149838255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699073 | AGCTTCTAGTTTCTG[C/G]TAATAGCAGACTAAG | 5607 |
rs149847103 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678489 | TGAGACATGTAAAAG[G/T]TCAGAGCAAATTAAA | 5607 |
rs149847290 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758890 | TTTTGGCATCAAAGG[A/C]AGAGGTTTTTTATAC | 5607 |
rs149861238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545729 | GGGCAAGTATCTTCT[C/G]TATCTCAGTTTCTTT | 5607 |
rs149870804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658325 | TTTCTTTCAGTTTTT[C/T]ATGTATGTGACTATA | 5607 |
rs149880606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613855 | AGAAGGGAAGAAATG[G/T]CTCACTTTTCAGAGG | 5607 |
rs149891559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733464 | CACATAAGAATGGCA[A/T]TCAAATAAATTATTG | 5607 |
rs149902198 | in-del | -/TAATAAGCATACT | 0.0693013 | 0.172766 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769853 | TATTTACACAAAGGG[-/TAATAAGCATACT]TCATAAGCATACTTC | 5607 |
rs149938855 | snp | A/G | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807577 | CATTTTGCAGGTGAG[A/G]AGCTGAGGCTCCAAG | 5607 |
rs149941528 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727594 | GAGTTTTTACATCTC[C/T]GTCTAGAAGAAACTG | 5607 |
rs149955837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600682 | TCTTTCTTTCTTGTG[C/G]AGATGAATGAACAAG | 5607 |
rs149974133 | in-del | -/T | 0.274661 | 0.248781 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660282 | CCTCCAAAATGTAGT[-/T]GTTTTTTTTGTATGT | 5607 |
rs150005821 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721488 | TACTTGGCACTTTTC[A/G]TATAGGCATAATGAG | 5607 |
rs150007760 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632849 | ATGAAATCCAGAGTT[C/T]TTCTTCCATATCACA | 5607 |
rs150017445 | snp | C/G | 0.030278 | 0.119257 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592012 | GGTACTCTGGAGACT[C/G]AGGCAGGAGAATCGC | 5607 |
rs150024956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784406 | CACACAAACAAACTT[A/G]TAGGATTTCAGCAGA | 5607 |
rs150028965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667406 | CATGTACTCATTTTT[C/G]CTTTCTCTAAATGAA | 5607 |
rs150039200 | snp | C/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541292 | GTAACTGAAAATGAC[C/G]AACATTAATTTTTTT | 5607 |
rs150055474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718194 | AATGTGAGTGAAGTT[A/G]AGCTCAATAGACTAG | 5607 |
rs150066544 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800297 | GCAAGACTTCAATAT[C/T]AATGTAGAAGTGGGG | 5607 |
rs150068564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587649 | GAGATTTGTCTTTCT[A/G]TAGCGCCCACTCATA | 5607 |
rs150076440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628972 | ATTTTGGCAATTTCA[A/G]CAATCAGTCTTCAAA | 5607 |
rs150112434 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570320 | ATAACATGAGCCTAT[A/C]AATAGGGCCCAGAGT | 5607 |
rs150119642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766243 | GAGACTAGACTCTCC[A/G]ATTGAGGCTTTTGGT | 5607 |
rs150130354 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714136 | CTTGTTGAGCCTACA[A/G]TGTATTAAGGGAGGC | 5607 |
rs150132249 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624967 | TTAGGTCCTAAAATA[C/T]GCATATTCTGTCGCG | 5607 |
rs150138148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745288 | TAACAATATTATTGC[A/G]TTCCTCTGAACTCTG | 5607 |
rs150141462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586276 | TTGCACATGGAATAC[C/T]CTCTCTTGACATATT | 5607 |
rs150162598 | in-del | -/AACTC | 0.23846 | 0.249734 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603087 | TGGTGAAATACACAT[-/AACTC]AAGTTAACATTTTAA | 5607 |
rs150173492 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760946 | CGAGTTGCTGTAATC[A/G]TTTTGCCGGCTGTTA | 5607 |
rs150182570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750093 | TGTTCAATTTAAAAT[A/G]TCTTACTTGTTTAAT | 5607 |
rs150184841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662314 | GCTTCCTTGATCAAC[C/T]AGAATTCTTGCATAT | 5607 |
rs150194386 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615762 | ATTTAGTTACTGAAA[C/T]CATATCATTGCATTA | 5607 |
rs150277173 | snp | A/C/G/T | 0.00319098 | 0.0398384 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691018 | TACCAACTTGAATTC[A/C/G/T]TAGAGCCTCCCAATA | 5607 |
rs150288510 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593541 | AATTTTGATTCAAGT[A/G]AATGGACACATCTGA | 5607 |
rs150318116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634503 | TTATTAGATATTTGA[G/T]TTTTATCTAGTACTA | 5607 |
rs150319365 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606781 | ACTGATGGTCATTTG[C/T]ATAAAATGAGAAAAT | 5607 |
rs150326900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724968 | TCTGTCTTCTAACTC[C/T]AAAGAGGTCAGACCT | 5607 |
rs150339140 | snp | A/T | 0.0414363 | 0.137845 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671948 | ATAGTTTACTGAGAA[A/T]GATGATTTCCAGTTT | 5607 |
rs150349818 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786774 | CAAAAATAGAGTATC[A/G]CAAAGCATGAAATTT | 5607 |
rs150380460 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719350 | AACCAGGCACCTCCA[G/T]GTTGACCAGTCTCCA | 5607 |
rs150381998 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802243 | TAAAGCCCAGGTGGA[A/G]GAGGGAGCGGTGAGC | 5607 |
rs150390026 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708047 | CAGGCTAGGCCTGGC[A/G]GCTCATTCCTGTAAT | 5607 |
rs150400737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791506 | ATAGGGCTTTTGGAG[A/T]TCACATGAACTAATG | 5607 |
rs150402318 | snp | A/G | 0.000115469 | 0.00759743 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563326 | AGTGAGAAGTGATGA[A/G]GAAATGAAGGCAATG | 5607 |
rs150402971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580909 | AAGGTTTAAATGCAC[A/G]TAACATGATGTTTAG | 5607 |
rs150409092 | in-del | -/TGAACTCC | 0.296364 | 0.245663 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551416 | AGCTCACTGTAACCT[-/TGAACTCC]TGAACTCCTGGGCTT | 5607 |
rs150412160 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776737 | GACCATTTGCTTCTC[C/T]AAACCACAAGGAATT | 5607 |
rs150415439 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654836 | GAGGCCGAGGTGCGC[A/G]GATCACCTGAGGTCA | 5607 |
rs150463052 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771971 | TCACCTCCATCCCAT[A/G]TGTGAGTGCTTCATC | 5607 |
rs150488177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638481 | CTACCAGTGATGGGC[A/C]TTTAGGTTGATTCCA | 5607 |
rs150497391 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665170 | TCAGGCGGGAGCCAC[C/T]GCGCCTGGCCAAAAG | 5607 |
rs150520859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618496 | AGATGTATGTCTGTA[A/G]CCCTGGCCTGTGTCC | 5607 |
rs150536699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799308 | AAGACTCCACATCTT[A/T]GGTGCAAGCACCTCC | 5607 |
rs150580099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736006 | CTAAAACAGCATATT[A/G]TATTTGGTGTTGTTC | 5607 |
rs150636060 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608852 | TGTTCCCACTGGGTT[A/G]TGTTCCCTGGAGGAG | 5607 |
rs150657744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562298 | TAGCCATAAGTCATT[C/G]TTAGACATGCTTGGC | 5607 |
rs150679608 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545476 | GTCTACCTCTCTGAG[A/C]CTTAGTTTCCTTATT | 5607 |
rs150694477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721014 | ATAAAGCAATTAAAG[C/G]AACAGCATTAGGATA | 5607 |
rs150695874 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804139 | TCTCCAGTGCCGTCA[C/T]GACCCCCCGCCTGCC | 5607 |
rs150712960 | in-del | -/T | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761303 | TAACTAGTTTTAAAC[-/T]GGTGTAGTGTCTCCT | 5607 |
rs150713138 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658555 | TTTATCTCTACAGGG[A/G]GATCTTTGGATGTAT | 5607 |
rs150717460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793760 | TATACTCTTTGATCA[C/T]GTTGTATATAAATGT | 5607 |
rs150727580 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657516 | AATAAAAATGTAATT[C/T]TGGTAAATAAGGGTG | 5607 |
rs150731145 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583513 | TTGTTTCTAGTTTTT[A/G/T]GTAGTCTTTTGCTTT | 5607 |
rs150766327 | in-del | -/A | 0.078151 | 0.181571 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668822 | AGAAGTTTATAGAAG[-/A]AAAAAAAAACCTATA | 5607 |
rs150781116 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740689 | GATTTATATACTTCT[C/T]GGTCTTCTCTCATTT | 5607 |
rs150782913 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650680 | AGTGTTGGAATTATT[C/T]CACTTAGTCATGATG | 5607 |
rs150801249 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799506 | AGGAAGCTGCAGACA[G/T]CTGCCCTGTGTTCAA | 5607 |
rs150812954 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632359 | CCTGTCTCAGCCACC[C/T]GAAGTCCTGGGATTA | 5607 |
rs150854339 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767815 | ATCCACCTCCGTTTT[C/T]CATGTCGTCTCTGTG | 5607 |
rs150855908 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688633 | CTTGGTTGATTACCA[A/G]TTGATAATGATAATA | 5607 |
rs150865396 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626969 | ACAGAGTCTCGCTCT[C/G]TCACCCGGGCTGTAG | 5607 |
rs150875137 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717357 | AATAGGAAGTAGGTA[A/G]GTAAGGATCTCATCT | 5607 |
rs150888125 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587467 | GCGAATGAGCAGAAG[C/T]TCCCATCTAATCCTG | 5607 |
rs150905488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763470 | TTTTCTCCCCTGTCT[A/G]CATTCTGTTACAGCA | 5607 |
rs150947915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742790 | AAAATGTGCAATTAC[C/G]AACAGGAAGATTTAC | 5607 |
rs150961539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609721 | TAGAATAGACTTTGC[A/G]TATTCTATAAAAAAT | 5607 |
rs150969090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728958 | TGTCTCTTTCGTATT[C/G]TTTTGCTTTCATAGT | 5607 |
rs150973341 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564353 | AATCATTTGGAATCA[C/T]GTGGAAATGATGGAA | 5607 |
rs150980322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759989 | AAAGTGTTGGGAATA[C/T]ATAGTTGAGATCCTG | 5607 |
rs150981469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680200 | ATTGTATGGATATAT[C/G]ACATTTTGTCTGCTT | 5607 |
rs150991513 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624397 | AGCTGGCAGTGACTT[C/T]AGAGCCTGTCCCATT | 5607 |
rs151016055 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605346 | GCGTGAATCACCACC[A/C]CCAGCCAGCCATGGG | 5607 |
rs151020453 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805265 | ACCTCGAATGAGAAG[A/G]TTGGGGGCGGGCACT | 5607 |
rs151023812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596764 | TTTGCTATCTTGGCA[A/G]TTGACATGTAATTGT | 5607 |
rs151032411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795636 | CCCTTAGAACATGGT[C/T]ATTTGGTTTTTCCCC | 5607 |
rs151035160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713278 | CTACCTTTTGTCTCA[C/T]TGGAATGTACAAGCT | 5607 |
rs151044548 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662026 | TCCTGTCCAGAATAC[A/G]TGTGTTTTATTGTAA | 5607 |
rs151045078 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584841 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 5607 |
rs151046977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552261 | CATCTGTCTGAAATA[C/T]ATACTAGTGTTGCAA | 5607 |
rs151083960 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790613 | AGTTGGGTCTTTAGG[A/G]CTGAGGCTCAGAGGA | 5607 |
rs151097013 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652445 | CTTCCATTCGTGGAG[C/G]AAGAGAGAGAGGAGG | 5607 |
rs151162362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784037 | TCCTGTTTTATAATC[C/T]TTAAAAAATTGATTT | 5607 |
rs151170066 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690436 | AAGTGGTATATTTAA[G/T]GTTTAATATGATGAT | 5607 |
rs151171353 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648604 | TTGAAACAGAGTCTC[A/G]CTCTGTCGCCTAGGC | 5607 |
rs151175877 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573691 | TAAGGGAACAGGTTA[A/G]TAGCATTTACCAAAC | 5607 |
rs151190253 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718917 | GTTACAAACATTCCA[A/T]TTATACTTTTAGTTA | 5607 |
rs151210048 | in-del | -/AC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556437 | CTTTAATGAGGTTAG[-/AC]ACACACACACAGTTA | 5607 |
rs151222203 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733199 | TCTGAAATCCTTGAA[C/G]ACATCAGACTTGATC | 5607 |
rs151226453 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640144 | CGTGATTCCTGCAGA[A/T]CCTTGCATATAGGGT | 5607 |
rs151232829 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765146 | CCAGTGGATCACGAG[A/G]TCAAGAGATGGGGAT | 5607 |
rs151236772 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558372 | GATGACTTCTTAAAA[C/T]CTCAGCTTGGTTTAG | 5607 |
rs151326361 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543451 | ACTCCGGGCCGCAGT[C/T]ACTCTTCAGGGATGT | 5607 |
rs151330052 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580291 | TGTTTGCTATTTCCA[C/T]AGTCTCTGTGATTTC | 5607 |
rs180680972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581754 | AACCAGTAGGCTCCT[A/G]TTTGCACTGATAAAG | 5607 |
rs180685949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563639 | TTTTTTATGCAGTAC[C/T]TAAAGTAACGGCTCA | 5607 |
rs180687343 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636466 | TAGTGGCCTTATCTA[C/T]TTATTCCATCATATG | 5607 |
rs180698537 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634895 | GAGAGTATTGAGACT[A/G]TTTACATTTCATATG | 5607 |
rs180709748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618752 | TGGGTTCTTCCTCAA[A/G]AATATTTCAAGAAGC | 5607 |
rs180762938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571728 | AGCAGAGGATACAGA[A/G]GCATAAACAATTGTG | 5607 |
rs180767178 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552114 | TGATCACACTTTTTA[C/T]TTTGTATGTTTCTCT | 5607 |
rs180781459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768007 | CAGATATGCAAAAAC[C/G]AAGAAACATTTTGTT | 5607 |
rs180783810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720191 | AAAGTTACTCAGCTA[A/G]GGTTTTTGGTTTAAT | 5607 |
rs180788436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738435 | CACTCAGTGATTCAG[A/G]GTAGAGGGCATAGGA | 5607 |
rs180794817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761824 | TTTTTAATATAATTT[A/G]TGATCTACCTTTAAG | 5607 |
rs180798132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777742 | GCTTTAGTAATTGTT[C/T]AAAAACATGGGTTTT | 5607 |
rs180804590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653119 | TGTTTCATCTAGGTT[A/G]TCTAATTTATTGATA | 5607 |
rs180805856 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795804 | TATCAATTTCTAAGA[C/G]AGGTATGCTAAAATC | 5607 |
rs180810628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784640 | GGAAGTAATTACCAA[C/G]AGTTTGCACCTGGTC | 5607 |
rs180824712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693289 | TAAGTGAATTGTTTA[A/T]GGTTATCTGCTATAA | 5607 |
rs180848911 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728035 | AACATTTGAGCCACA[G/T]ACAAATAAATCTGTC | 5607 |
rs180866526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673422 | TTTAAGATTAAAAAT[G/T]TTATAAGAATATTTG | 5607 |
rs180869756 | snp | C/T | 3.30028e-05 | 0.00406205 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703334 | CCTTCTGATTTCTTG[C/T]AGCCTGAAAGGATTT | 5607 |
rs180879451 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780765 | TGCAGGGATAATATT[A/C]AAAACATTTAACAAC | 5607 |
rs180890310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748365 | AATTGCATTTTGAAG[A/G]AAATGCAAACCTTTA | 5607 |
rs180986310 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648688 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 5607 |
rs180987639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614094 | GTTTATTTTCACACA[A/G]AGCTTGTTGGGACAT | 5607 |
rs180988942 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566648 | CCTATATCTCTGCAT[A/G]AGAATAAAAACAAAT | 5607 |
rs180997304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706954 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGCAGTG | 5607 |
rs180999525 | snp | C/T | 0.000576497 | 0.0169681 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586803 | TAATTAGAACTGTGT[C/T]CTCAGAACACAAGAC | 5607 |
rs180999744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629794 | TTACTTACTTCCTTA[C/T]ATTAATATTTTTATG | 5607 |
rs181000311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687563 | CACCTAGTACCATAT[C/G]TGGCACATGGTAAGG | 5607 |
rs181008039 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547233 | TACTAGTCTTTCAGG[C/T]TTGTCTTTATCTCTG | 5607 |
rs181010214 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622229 | GAAAGTCAAAGAAAC[A/T]ATATAGGACCTGAAG | 5607 |
rs181015531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637547 | AGATCGTTTCTTCTG[A/G]GCCTTTCTAGTGGTT | 5607 |
rs181019190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604350 | GTATTTTCCTTGTTG[C/T]CTCATTTCCTAAAGT | 5607 |
rs181027273 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668055 | AATTGAAGCACAGCA[C/G]TTGCTATTCATAATG | 5607 |
rs181073501 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578009 | TGTCTCAAAAAAAAA[G/T]AAAACCCCAATTTGT | 5607 |
rs181074543 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595786 | GAGAGCTATAAATCA[G/T]TCTCACTGATGTGTT | 5607 |
rs181086257 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559297 | TGTTTCTCTTGAAAG[C/T]CTTCTTGAGCCCCTG | 5607 |
rs181091134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791444 | CATCATTACCATCTT[A/C]GAGTGCAGTGTCCTT | 5607 |
rs181126733 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722417 | AACCCTACTTCAAGA[C/T]GCTTTGTGTTTCTGT | 5607 |
rs181144155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742989 | GTATTTTGTGTGAAA[A/G]TGCATTGTCCTTGAT | 5607 |
rs181148638 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765295 | ACCCAGAAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 5607 |
rs181159086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780517 | GTAGACACTAAACAG[A/T]TAGACAAACAAGACA | 5607 |
rs181165737 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799946 | ACGCAGAGTGGGGGG[C/T]GGTGGGGGGGATTGT | 5607 |
rs181183741 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756309 | ACAGGAAGAAAGAAA[G/T]AAGAGACAAAGTAAA | 5607 |
rs181188172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774033 | TAAATAAAACATCTG[C/T]AGATCACACATACGC | 5607 |
rs181219518 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600749 | GAGGCACAGTCTACA[A/G]GTGAGTAGTCAATTT | 5607 |
rs181230918 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553812 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATG | 5607 |
rs181232855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563120 | GAGATTCTGATCATA[G/T]TCCAAATGGAAAACA | 5607 |
rs181233929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581420 | CAGTACTATCCTTGT[A/G]TCAGATATGATTGTT | 5607 |
rs181272490 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565641 | TCAAATTCAGTGTTT[A/T]ATTATTTTTGTGTTG | 5607 |
rs181282197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683212 | GTTCAGTGGCTATAT[A/C]CTAGGATTGTTGATA | 5607 |
rs181309684 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738004 | TTATAGGAGTGCATC[A/C]CCATACCCGGCTAAT | 5607 |
rs181322764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591754 | TCAGGTAGATATTCA[C/T]GGGTATAACTCATTA | 5607 |
rs181324840 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633818 | TTTAGGCAAAAACCA[A/T]GTAACTTGTATAATA | 5607 |
rs181327722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609191 | TTACCATAAAAACCT[C/T]ATGTCAGGTGTTGCT | 5607 |
rs181330364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573896 | ATCTCCTCCATATGG[C/T]TTTTTGCTTTGTTAT | 5607 |
rs181331237 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608230 | GTGTCTGTCACTTTT[G/T]GATTCTGGATTCCTG | 5607 |
rs181345108 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673036 | ATCTCTGTTTTGGTA[A/C]CAGTACCATGCTGTT | 5607 |
rs181349004 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805334 | TCCCCCACAGTTCTG[A/T]CCTGTGGTCCAGAGG | 5607 |
rs181350021 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661312 | CATTCTATTTTTCTT[C/G]TCATTTCTGAAGCAG | 5607 |
rs181351628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626459 | TTGAACCTGGGTTTC[A/G]GAGGATGCAGTGAGC | 5607 |
rs181355562 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644132 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 5607 |
rs181387962 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719884 | TCTTTAACTCAGAGT[C/G]TCTCACGAATTTCCT | 5607 |
rs181404659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761178 | GGCATTATGATTTTC[C/T]AAATCCTGATGAACA | 5607 |
rs181426202 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777426 | AGAAGAAGCAGCATC[C/T]CGGTTTGAGATCAAT | 5607 |
rs181440807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595422 | AAACCATTATTGCTT[C/T]GATTTGTGAAGCAAA | 5607 |
rs181441077 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548957 | GACTATTATGCAAAT[C/T]GCCACTGCAGCAAAA | 5607 |
rs181444357 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567738 | TACATATTCTGAAAA[C/T]TAAATACCTGATCAT | 5607 |
rs181444378 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612375 | TGTTCTAACACAGTT[C/T]ATATATTTTTGTAAC | 5607 |
rs181449782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652587 | CCAAACACCTCTCAC[A/G]AGGCCCCATCTTCAA | 5607 |
rs181456695 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734605 | ACTAATTCTAATGTT[G/T]ATTGTTTACTGATGT | 5607 |
rs181458288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755753 | TGGTTAAATAGAGTC[A/G]TAAGAACTTGCAGAA | 5607 |
rs181459720 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617684 | TATTTTCACATATTT[A/G]TTTTCCTTACTTTTA | 5607 |
rs181460663 | snp | C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547448 | GTAAACTTCGGTTTT[C/T]TTTTTTCTTTTTTTT | 5607 |
rs181465630 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772328 | CCAAAAAAAAAGGTA[A/T]ATTCTCTAAATATAA | 5607 |
rs181470087 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587890 | TGGGTTCTACCTTCT[A/G]AGTAGCTCTGCGTCT | 5607 |
rs181475689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648209 | AGAAAGAGACTTCCT[A/G]CCTATTAGTACTCAC | 5607 |
rs181475887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629356 | TAGTTCCTGTTCCAT[A/G]GAAAGTTTAAAGCAT | 5607 |
rs181477620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789783 | GAGGATTAACACTTC[A/T]TTCATATGTTTGTTG | 5607 |
rs181493634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693007 | AGTGATAGTGACCCA[A/T]GAGCATGCTGTGATG | 5607 |
rs181501706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622865 | GCACTTTGGGAGGTC[A/G]AGGCAGGTGGATCAT | 5607 |
rs181523792 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768913 | TGGTGGTGGTTGTTT[G/T]TTGCTGTGTAGTTTT | 5607 |
rs181533461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558826 | CTTCAGTCTCTTTCC[A/C]CTAGAGTGTATGTTC | 5607 |
rs181553067 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687110 | CTGCAGTAAAATTGA[C/T]TTTTTTAATGAGATT | 5607 |
rs181560153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666862 | TGAGTGTGCACCTAC[A/G]TCTGTCTCAATGGAA | 5607 |
rs181564558 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795635 | TCCCTTAGAACATGG[C/T]CATTTGGTTTTTCCC | 5607 |
rs181579094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706232 | TAAAAAGAGACTCTT[C/T]GTAGTGTAAGGAAGG | 5607 |
rs181622565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604787 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGGGGCAG | 5607 |
rs181624425 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620122 | AACGCCTGTAATCCC[A/G]CACTTTGGGAGGTTG | 5607 |
rs181630809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635141 | TACATCATCATATGC[A/G]ATAAACCCCAAAATG | 5607 |
rs181643349 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653604 | CCCAGCTAAAAAAAA[A/T]TTTTTCATTTAAAAT | 5607 |
rs181657640 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674503 | AGCCCATTAACAGGG[C/T]AAACAAACTCTGACT | 5607 |
rs181700638 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657283 | GAAGTTGTTACTGGT[A/T]CATGTGGATGGGTTT | 5607 |
rs181704928 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698436 | CTCAAGTGATCCACC[C/G]TCCTTGGCCTCCCAA | 5607 |
rs181710359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721432 | CTCACATTTAGGCTC[C/T]TTCTACACAAAGAAA | 5607 |
rs181719646 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709478 | TTCAAGACTTCAGGG[A/C]AAAAAAAAAAAAAAA | 5607 |
rs181720455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764876 | CAGCCTTCTCCCTTA[C/T]ACAAGCAGAGTTCTG | 5607 |
rs181724213 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573553 | ATGAGATTTGTGGGC[A/G]GGTACACAAATCCAA | 5607 |
rs181727119 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552906 | TTGAGAGTTGTCATA[A/C]TTATTGAAATCATAT | 5607 |
rs181763646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590816 | CTACTACTGCCACCA[C/T]AGTATAATAATAACC | 5607 |
rs181766539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712311 | GGAAACAGCCTAGCT[A/G]AATCATGCTCCCAGG | 5607 |
rs181769386 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694038 | GGGGGCAGTTTTCTA[G/T]AGAACTTGTACCTCT | 5607 |
rs181769421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760924 | GGGCACTGCTCTGCT[C/T]CACTGCCGAGTTGCT | 5607 |
rs181773668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728264 | GCTTTTTCTTGATAC[A/G]CTTTTTAAGCTCTTA | 5607 |
rs181779511 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776791 | TCAGAGTTATTTGGT[A/G]GCTAAGGTCAGGATG | 5607 |
rs181785727 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794892 | GCTGCTTCTTGAAAT[A/G]AGATGAGACAATAGA | 5607 |
rs181787144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749054 | TAAAAGGGCTCAAAA[A/G]CTCTAGGTCAACAGT | 5607 |
rs181811236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679920 | CATAACCATAATCCA[A/G]TTTTAGAACATTTTC | 5607 |
rs181815509 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639260 | CCCTTTCTTTTCCTT[A/C]CACCACTCTAATCCA | 5607 |
rs181824274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643522 | CGTGATCTCAGCTCA[C/G]TGGAAGCTCCGCCTC | 5607 |
rs181828648 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786018 | TTTAGCTGTTAGGTT[G/T]TTTTTTTTTTTTTAA | 5607 |
rs181853124 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742185 | CGTGAGCCACTGCGC[A/C]CGGCCAAGAAAGAAC | 5607 |
rs181859214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682804 | CACCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 5607 |
rs181859501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719024 | AACTTTATTTTTGTA[C/T]CCATTAATCATCCCC | 5607 |
rs181866515 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591848 | CAGGGGTGGTGGCTC[A/C]CGCCTGTAATCCCAG | 5607 |
rs181879575 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715829 | CTCCCATGACTTTCT[A/G]TTCAGTATAAAGAAG | 5607 |
rs181883442 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715407 | TGTCAGTGATTGTAG[A/T]GAATGTGAAACTGGC | 5607 |
rs181887969 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698139 | CATAAGAATTATAAA[A/G]GGGGTCTGGAAACTT | 5607 |
rs181893380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608492 | AGGTATGCACAGGAC[C/T]CCACAGTCTGGGGCC | 5607 |
rs181894808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583485 | TGTGTTTTTTTAATA[C/T]GCTATGGTGTAATTG | 5607 |
rs181896023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733775 | AAGTTAAACATAGGT[A/G]GATAATAAGTGAAAA | 5607 |
rs181943655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656323 | TCATGGGGAAACCTT[C/T]TAATTTTTTTTTTTT | 5607 |
rs181947007 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629921 | AATATCTAGTCCCCA[A/C]AGTATATGTGTAAAG | 5607 |
rs181953247 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638737 | TTGCCAGCATCTGTT[A/G]TTTTTTGACTTTTTA | 5607 |
rs181954889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678158 | CATTAGAATGCAGTC[C/T]CCAATAAATAACTAG | 5607 |
rs181994152 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785064 | CCTACCTCAGCACCC[A/G]CCCTTCCTTGAGTAG | 5607 |
rs182021991 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567283 | CTTGTAAGTTATGTT[C/G]TTAGAATATTCCACT | 5607 |
rs182030337 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692182 | TTTCCTGAAAAACTA[G/T]GGATAGGATGATGGG | 5607 |
rs182054841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780802 | AGCATGAGGATTACC[A/G]TTCAGAACCAACACC | 5607 |
rs182061197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801001 | TTATTTTTTTAAATC[C/T]GTTTTTAAAACTGTA | 5607 |
rs182092045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626289 | GCAGTTTGGGAGGCC[A/G]AGGCTGGTAGATCAC | 5607 |
rs182099369 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660860 | CTCAGTGTGTTTTCC[A/C/T]AACAGAATGAGAAAA | 5607 |
rs182105085 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555790 | TTTGTATTTAATTTC[C/T]TTTTTTTTTTTGAGA | 5607 |
rs182114382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702815 | AAAGGAAATAGGAAT[A/G]TGTATTGCTCTGATC | 5607 |
rs182117102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564857 | TTCATTATGTATTCA[A/G]CTTAACCACATGCAA | 5607 |
rs182120787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544609 | TGGTATTCATTTGAG[A/G]TAGACAGGGTGCCTT | 5607 |
rs182123638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668742 | AAATGCAAGGGTAAT[G/T]AGAATAGAATTTAGA | 5607 |
rs182158770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707696 | AAGGGGAAGGGGGTG[A/G]GGTTTCACACAAAGG | 5607 |
rs182162934 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771762 | ATTAAATCTATTTTT[A/T]AAAAAGTATTGTCAG | 5607 |
rs182164221 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763387 | CTCTAAACGAGACTC[A/T]TTCTCGGACCAGGAG | 5607 |
rs182172016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743572 | TAAAAGTGATTTGTT[C/T]GGGAACTCTTTAAGT | 5607 |
rs182188650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675826 | AGGATTTGATCATAG[C/G]CAGAGTCATCCCTTT | 5607 |
rs182193119 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616188 | ATAAAATGTCACACA[A/G]AGCAAAGAAGCATCA | 5607 |
rs182196046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604689 | ATCACGAGGTCAAGA[A/G]ATTGAGACCATCCTG | 5607 |
rs182199278 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805118 | CCACCCCAGTCTCAG[C/T]GGGTCCCTGCCCGGG | 5607 |
rs182240383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737242 | TATGGATCCCTGGGG[A/G]GAGAATGGTCCTCAA | 5607 |
rs182252252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602605 | TTTACGAGACATAAT[A/G]TTCTAGATGTTGACA | 5607 |
rs182266422 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798592 | CCATTTCTGGCCTAT[C/T]ACTCTGTGTAGAAAC | 5607 |
rs182269436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769026 | CTGGCTTTCTCATAT[A/G]AGGAGTCTGCCTAGA | 5607 |
rs182274322 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584740 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 5607 |
rs182277999 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683721 | GCCGAGATCGCGCCA[C/T]TGCACTTTAGCCTGG | 5607 |
rs182287337 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621048 | TGCTATTTTAGACTG[A/T]ATTGGGAGAAAATTT | 5607 |
rs182292128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654495 | TTCTGCCAATCTCTT[A/G]TTTAATTAGAGTGCT | 5607 |
rs182294768 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636057 | AATCCACCCGCCTCC[A/T]CCTATCAAAGTGCTG | 5607 |
rs182325326 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548449 | ATTCCAGTTATTGGT[C/G]TTTTGTTTTATTTAT | 5607 |
rs182328731 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647302 | GTTATAGTAGAATGT[A/C]AAAAATTAAAAATCT | 5607 |
rs182365061 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745572 | ATATGCCTAATATAA[A/G]TACAGCCGAGTACAT | 5607 |
rs182375296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591991 | TGGCACATGCCTATA[A/G]TCCCAGGTACTCTGG | 5607 |
rs182378860 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766448 | TCTTCAGCCCACATT[C/T]ATATTTTTGAAATAT | 5607 |
rs182384179 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782065 | TTAATCCTCTGAATC[C/T]CCAGTGGAGCAGCAG | 5607 |
rs182389001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802501 | CAAAGTCTGTGGACT[A/G]TAATAACTTCAACCC | 5607 |
rs182395447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605416 | TGAACTAACTTTGAG[A/T]AATTCTGCCTTTATA | 5607 |
rs182397019 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562076 | CCAAGAGTGAACAAA[A/T]ATAATAATTCCGATT | 5607 |
rs182399911 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555264 | TGAAGGGGCAGCAGG[A/C/T]GTGTCACATGGCGAG | 5607 |
rs182403672 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568557 | GCCTGGATACAGACT[C/G/T]TCAGTCTCTTTGCTC | 5607 |
rs182405863 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649301 | TGGCTCTTATCAGAT[A/G]TGGGATTTCCAAATA | 5607 |
rs182406192 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588842 | TTTTTTAGAGATGGG[A/C]TCTCCCTCTGTTGTC | 5607 |
rs182409882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688214 | GGGCATGGAAAAGAG[C/T]GGCAAGGTGAGAGTA | 5607 |
rs182422220 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723227 | TTGTTAAAATACAAA[G/T]ATTTTTATCGTGTTA | 5607 |
rs182423159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623404 | CATGAAGTAATACTA[C/T]GTGTTTAAGTTTTTC | 5607 |
rs182427568 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709067 | ATGGCAGTTTGACTT[C/G]ATGGGAAGAATTTGG | 5607 |
rs182429542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639813 | TCACTTCAACACTTT[G/T]ATTCACGTATTCCTC | 5607 |
rs182437408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789043 | TCCTTCCAATCCTCC[A/G]TATCTTCCAGCCCTA | 5607 |
rs182439634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724866 | AGTCTTTCAACAGCC[C/T]AGTGGTGACACTCTG | 5607 |
rs182440696 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714504 | TGTGGTTGTGGCTTT[G/T]TTTGCTTTTCTAGCC | 5607 |
rs182443123 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622720 | ACACATAAATACTTT[C/T]CTGTAGTGTGCCAAG | 5607 |
rs182446083 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579709 | AGAGGAAAAAAAAAA[A/C]CCTTGCTCTTGTAAT | 5607 |
rs182452598 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587545 | ATCTCTTACTGAACA[A/T]CCCTGTCGGAGGAAT | 5607 |
rs182472817 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695856 | TTGGATTGACAAAAC[G/T]AAAATTGCTTTGCTT | 5607 |
rs182501867 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729943 | ACTATGCTGAACTCC[C/G]TAGTTAGCAACAACC | 5607 |
rs182521916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770079 | AGTTTATTAATTCAT[C/T]GGATTTTCAGTAAAT | 5607 |
rs182532521 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628826 | AATTTTGGTCATGGA[C/G]GAAACTTCAGTGGTC | 5607 |
rs182539742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593681 | TTTGATAGCCTTGGA[A/G]GCAGGCGCCTGTCCA | 5607 |
rs182545187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680287 | TACTACTTTTCATAC[A/C]CAAGTCTTTATGTGG | 5607 |
rs182545764 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610154 | TTTCCTAACTATTAA[A/C]CCAAGTTATTTTTGG | 5607 |
rs182547962 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765833 | AAGTGCTAATAACAA[A/C]ATACCCAGAGAGAGT | 5607 |
rs182555448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647291 | GCTCTAAATTAGTTA[C/T]AGTAGAATGTCAAAA | 5607 |
rs182565471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685253 | GATAAGATTGACAGC[C/T]GACTTCATGTCACAA | 5607 |
rs182566923 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729536 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 5607 |
rs182570261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664148 | TTTCCCACAAAGCCT[C/T]ACACAGAAATGGGAG | 5607 |
rs182610122 | snp | G/T | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542530 | TCCCCGACTCGCCAC[G/T]CGCCACGCGCCGCGC | 5607 |
rs182655157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574407 | TGAAACCCCATCTCT[A/G]CTAAAAATACAAAAA | 5607 |
rs182675556 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704706 | GGTCAGATCTCAGAA[C/T]TGAGTCTCCCAACAG | 5607 |
rs182675606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750957 | ATGGGTATATTTGGC[A/G]TCACATACAAAATAG | 5607 |
rs182683284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769774 | TTTTGGAGACAGGAG[A/G]GACTTCGGGGCCTTG | 5607 |
rs182687527 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785903 | AGTACAGGCACTACC[A/T]CTAGGAAACTGGGCA | 5607 |
rs182699110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615607 | GCCATTAGTCCTAAA[C/T]GTGTTAATAAAATCT | 5607 |
rs182714315 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580510 | TTTCTTAAATACTAA[C/T]ATAAAGTCTTAATCA | 5607 |
rs182729387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564389 | GCTCTTGCTTTTCAC[G/T]GAGACCCTAATCTTA | 5607 |
rs182735669 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543240 | TTCACCCTCTGTCCT[C/T]TGCCCGTCACTCCCC | 5607 |
rs182746314 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713502 | GCACTTTGGAAGGCC[A/C/G]AGGCGGGTTGATCAC | 5607 |
rs182757659 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549314 | AGATTATATACCCTT[C/T]TTAGATTTTTGTTGT | 5607 |
rs182760752 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702963 | TGTGTAATTTGTTAC[A/T]CCACAACAAAGACCA | 5607 |
rs182766320 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752443 | CCAGCACTTTGGGAG[A/G]CCAAAGCGGGTGGAT | 5607 |
rs182797081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707997 | GTAGGAAACCGAGCA[A/G]AGGAATTTCCCTGAA | 5607 |
rs182812687 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645056 | AGGAGGCTGAGACAC[A/G]AGAATCGCTTGAGCC | 5607 |
rs182819064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724199 | TAAGTTTCCTAATTT[A/G]TAATACCTTGACAAT | 5607 |
rs182819642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650721 | TTTATATGTTCCTGG[C/G]TTCAGTTTGCTAGTA | 5607 |
rs182832603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715931 | GTCCCATCCCTGGGG[A/T]CACATAAGTAGGGAC | 5607 |
rs182845874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615275 | AGTGCTGGAATTATA[G/T]GTGTGAGCCACTGTG | 5607 |
rs182854029 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689843 | AGCACCTTCTTCCAG[A/G]AGTTCAAAATATTTG | 5607 |
rs182854990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630484 | AAAGCAAAATGGCTC[C/T]GTACACTGCTTAACA | 5607 |
rs182871567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650176 | ATATTGATCTTGTAT[C/T]CTGCAACCTTGCTGA | 5607 |
rs182879982 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689512 | TTTGAGACAGTGATT[A/G]AAACAGTCTTGTTGG | 5607 |
rs182885221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669401 | TCATAGGGAAGATGA[A/G]TTTGGGAGGAAGGCT | 5607 |
rs182904503 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786661 | GGAAAGTGGTGGTAC[A/C]ACAGAAAGCCAGCTT | 5607 |
rs182973647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574718 | CTAAAAATACAAAAA[C/T]TAGCTGGGCGTGGTG | 5607 |
rs182976288 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592732 | TTTTGATTACTAACA[G/T]GGTTTTAGTCTCTTT | 5607 |
rs182988178 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759122 | CTCTTAAATGTGTTA[C/T]CTTAAAAAATTCATT | 5607 |
rs182991761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555865 | CTCGGCTCACTGCAA[C/T]CTCCACCTCAGGGGT | 5607 |
rs182994520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597616 | ATGAACACTCTTCCT[A/G]TGCTTCATTTTGAAA | 5607 |
rs183015655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674835 | ATACACAGATGGCAA[A/C]TAAGCACATGAAAAA | 5607 |
rs183019740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635255 | CAGTGGTGCGATCTC[A/G]GCTCCGCCTCCTGGG | 5607 |
rs183051411 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712623 | TAGGAGAGAAATGAA[A/T]AAAGAACCAAGTCGG | 5607 |
rs183082451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775144 | CAGAATACCCCTTAT[C/T]GAATCATAAAATCAT | 5607 |
rs183091215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792828 | GCCCAAAGCGGCCCC[A/G]TATGTCTTTAATGAA | 5607 |
rs183094385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574815 | GATGTTGCACTGAGC[C/T]GAGATCGTACCGCTG | 5607 |
rs183104616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602451 | ATTTAAAAATGTTTA[C/T]TTAGACTCCTAACCT | 5607 |
rs183134070 | snp | C/T | 0.000559298 | 0.0167134 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630867 | GATCCCAAATGATTT[C/T]GTTTTTTTTTCTTCC | 5607 |
rs183137500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670093 | TAATACATCCACAGA[A/G]TGGAATATTACTCAG | 5607 |
rs183141720 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698928 | ACACAACCCCAGGAG[C/G]TATACGTATTACTAC | 5607 |
rs183149069 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735100 | CACTTATACACATTT[G/T]CTTCTTCCTAGGAAT | 5607 |
rs183162912 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711689 | CACACACACACACAC[A/G]CACAAAAGGATAATA | 5607 |
rs183197970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740234 | CTGGCATAGCATAAG[A/G]ACTTAATAAACATAT | 5607 |
rs183215698 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778789 | TTTCGGTTTACTTTG[A/G]TCCGGGGCTTACCTG | 5607 |
rs183216488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730998 | TAAAGGAGGTATGCT[C/G]ATCAAATGAGACTAT | 5607 |
rs183216679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778358 | TGATGTTAGATTTTT[A/G]TCTCTCCAACACTCA | 5607 |
rs183218148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753917 | ATGAACATTCATAGC[A/G]GCATTATTCATAATA | 5607 |
rs183223995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796946 | ACAGAATTTCTAGGA[A/G]CCGGCACACATTGTG | 5607 |
rs183231485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770423 | CCCAGGTATTCCTCT[A/G]CCCTCTCCCTCACTC | 5607 |
rs183253833 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560484 | AACAACTATTCATCA[A/G]TATGCCATATAAGCC | 5607 |
rs183276327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676156 | GATTCACCAAGCCCC[A/G]CAGTTAGCTCTGATC | 5607 |
rs183286146 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579305 | CAATTTTTCCAGACT[A/G]CTTGTTAACAGTTAT | 5607 |
rs183286942 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714172 | ATAAACAATAATAAA[C/T]ACTTATGTTTTTTGA | 5607 |
rs183291181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696065 | TAACCTATATTATTA[C/T]AGTACAGGTATGAAT | 5607 |
rs183296287 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654219 | ACTCCGTTGTTAGGT[C/G]CATGCATGTTTATAA | 5607 |
rs183304432 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695304 | GGATGGAACCTTATT[A/C]TAAACCTAATTCTAA | 5607 |
rs183332126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659789 | TCAGTTATCTATGGA[A/T]CTTGGCAAAAATAGA | 5607 |
rs183332768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560132 | ATTTGCTTAGTATGT[A/G]TTTCTGCTTTCTTAC | 5607 |
rs183344812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700391 | ATGTTTTAGACAAGA[C/G]TCATGTTTTTCCTAT | 5607 |
rs183349692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620567 | AAAGAATGGAATCCA[A/G]TTGAATTCAGGAAGG | 5607 |
rs183357238 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584222 | ATAACTTTAGGAAAT[A/T]TGAGGTTACTGGGTT | 5607 |
rs183360406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556494 | TTGTGGGTTTTTATA[A/G]AAAGCATGTATTTTT | 5607 |
rs183361506 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596099 | GTCCAGCTGCATCTT[G/T]TGGCTGTTATTTTGA | 5607 |
rs183364135 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766198 | CAAGACCCAGCTTGT[A/G]TCCCTTCAGCAGAAC | 5607 |
rs183365527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614713 | AATCAGGCCACATCA[A/G]CTTGTGGAAGAAATA | 5607 |
rs183368219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735690 | TCACAGAGTAGATAG[C/T]TGACGCTTGAGCCGA | 5607 |
rs183396147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680761 | ATTTATTGCATCATC[A/G]TTAAAAAGCCCAGCT | 5607 |
rs183399478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596673 | CCATGGGTTGTTGCT[C/G]TCTCTGTTTCTTTTA | 5607 |
rs183402166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659086 | TTTTTCATCAACTAC[A/G]TCTAGAAATTTATTC | 5607 |
rs183410533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625116 | AGCTCAATAAATTAT[C/G]TGATTCTGTACCAAG | 5607 |
rs183412105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699485 | GAGAAGCAGAAGAAA[C/T]AGGAAAAGTGGAACA | 5607 |
rs183449253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763226 | AAGTAGGTCAGTTCT[A/G]TCTGCATCATGAAAT | 5607 |
rs183463545 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798149 | CATATTCACAGTGTG[A/G]ACATGCTGCAGACTC | 5607 |
rs183487252 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802114 | CACGTGGGAGGGGCC[C/T]GGGAGTGTCCTGCTG | 5607 |
rs183495036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580075 | AATCAAACCACAGTA[A/C]CACCTACTGAATAAT | 5607 |
rs183537439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735348 | TTGAGATATCTGTAT[A/T]TGGCCAGTTAGGTTC | 5607 |
rs183537483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716481 | TAAAATTCTGAGTCT[A/G]TGATAATTTTGGGAA | 5607 |
rs183543173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622471 | TACCCATGAAATGGA[A/G]ATGAGTATAATAACT | 5607 |
rs183549401 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775022 | GCGAACACAGCAAGT[C/G]TCAGCCTAAGTAAAT | 5607 |
rs183559438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637619 | ATCATTCATTACTCA[A/G]CTGAAGACTCCAGGA | 5607 |
rs183565639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604356 | TCCTTGTTGCCTCAT[C/T]TCCTAAAGTGCTGCA | 5607 |
rs183571319 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655184 | TGTGTGTCCAACACA[A/G]ATTTAAAATTATGCC | 5607 |
rs183572719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705141 | GAGACAGTGATAAAA[C/T]GACATAAAATGCAGA | 5607 |
rs183577893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645898 | GGGTCATTCCTATGC[G/T]CCTCTTTTGAAAATA | 5607 |
rs183582107 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677935 | GCAATAACTGCCATT[C/G]AGGATGGCTAATTAT | 5607 |
rs183584218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720872 | TATATTAGGTGAAGA[C/T]TGTGAACTAAGCTGC | 5607 |
rs183584754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744727 | TTTTATCACCAGAGC[A/C]ATTGGCTAAATAGTT | 5607 |
rs183589144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67716950 | AGTTCCCATTTTGCA[A/T]ATGAGGAAACTTAGA | 5607 |
rs183604271 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781273 | TTAACCAGTCTAACC[A/T]GGAATTTTAAGAGCT | 5607 |
rs183606370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566999 | ATTAAACCAAAGTCT[G/T]TTGTCACACATTAGT | 5607 |
rs183639163 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541249 | AAAAGTAACTCAGAG[C/T]AAAGTATGCAGAAAA | 5607 |
rs183642543 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762431 | GAAAGGAAGCAATTA[A/T]AAATACAGTTTAAAA | 5607 |
rs183656735 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641257 | TGCTTTGGGTTTCTG[C/T]TGCTTTTAAACTAGC | 5607 |
rs183663206 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741525 | CTTAGGCTGCAGTTT[C/T]ATTGGACCAGTTCAA | 5607 |
rs183666215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697777 | AAAAAGAAAATATAT[C/T]AGAATGAAATAGCCC | 5607 |
rs183666293 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763678 | CAAACTCGATTTTCT[C/G]CCCAAGCAAGTACAG | 5607 |
rs183668532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787019 | TGATGGGGTAAAGTT[A/T]GCTGCATGGGGCCAG | 5607 |
rs183678205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779185 | AGCAAGGGGGCCCCA[C/T]GTAGGGTCCAGCTGA | 5607 |
rs183694411 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785839 | GAGCCAAGAAGCAAC[C/T]TGGGAAACTGGAAAG | 5607 |
rs183709542 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761244 | TCTATTTTTTCATTT[C/T]CTCTTCTTCCCTCCC | 5607 |
rs183712305 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684167 | TCTGCATTTATAGAG[G/T]GAAATCCTACAAAGC | 5607 |
rs183720008 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720265 | ACGCATATATATACA[C/G]ACACATATGCTTATA | 5607 |
rs183793613 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628419 | CAGGAGGCAGTGGCT[A/G]TGGTGAGCCAAGATC | 5607 |
rs183808431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702312 | TGTATAGAAATTCTT[C/T]AATAAATGCACACAT | 5607 |
rs183838181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563943 | TTATCTGATACTGAA[A/G]TAAACAAGAGAAAAG | 5607 |
rs183851441 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625449 | TAATTACTGTGGCAA[C/T]AACAAACTAATTTGA | 5607 |
rs183860205 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590139 | ATTAAAGTCAAGAAC[C/T]CTTGGATGAAGACAT | 5607 |
rs183862830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607421 | CTAAGGAATGAACCT[A/G]AGCTCATGGTTCTCT | 5607 |
rs183879055 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640869 | TTCTATTTTATACTA[C/T]TGAATTTAGAAAATG | 5607 |
rs183880107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642171 | ATTTTTATTTGTTTG[C/G]TGGTGTACATTTTTA | 5607 |
rs183881553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681635 | CAAGATAGCTTAAAC[A/C]CAAACCTTAAATTAG | 5607 |
rs183907673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663401 | ATTTTGGAAGAGTAC[A/G]TTGCCCAGTACTTTG | 5607 |
rs183937968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703995 | GAAGAGGATGTATGT[A/G]TTTAGCACAATTGCA | 5607 |
rs183941151 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738855 | TAGATGAGCAGCTTC[C/T]TCCTCCTGTCCACAC | 5607 |
rs183965945 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605715 | GTTGTCTCAAGGTCA[A/G]GCAGAGTCCATTTTG | 5607 |
rs183974386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659349 | AAAGTGATTGTACCA[C/T]GTACCATTTAATTAA | 5607 |
rs183988290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586683 | AATGTATGGGTTATA[C/T]GGTTTTGTAACCTAT | 5607 |
rs183992027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569331 | ATGCAATTTATCCAA[A/G]CAACTGATTACACAG | 5607 |
rs183993778 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782644 | TTAAATTTTGTTTCA[A/G]TCAACCCCTGTGCTC | 5607 |
rs184001755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546507 | ACCCTGGGCAAGTCA[G/T]TCGGTCTCTCTGGGC | 5607 |
rs184003885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727534 | CTGAAAATTTTGTGG[A/G]TTAGTAACAATTAGA | 5607 |
rs184004394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566252 | TGATCTCGGCTCACT[A/G]CAACCTCCGCCTCCT | 5607 |
rs184013224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747185 | GATGATCATCCCTGC[C/G]AAACTCAGGGTGGTT | 5607 |
rs184068737 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623808 | CTCCATGTTGGTCAG[A/G]CTGGTCTCGAACTCC | 5607 |
rs184082617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745685 | GCAATATATCTGAGA[C/T]AGAAAAAGGAGATAA | 5607 |
rs184103247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549884 | TGGGTTTACGTTGCT[A/G]GGCTAAGTGTGATTA | 5607 |
rs184124566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589112 | GCCTCCCAAAGGGTT[C/G]TGATTACAGTCATGA | 5607 |
rs184134445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767570 | TCTTTTTACTAATGG[C/T]TTTTGAGACAGTAAA | 5607 |
rs184137569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784439 | GTGCTTGTGAAGCCA[A/G]TGCCCCTGTAGGATG | 5607 |
rs184145327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804596 | GGAATGTGGAGGAAC[A/G]CCTCTACGCTCCCTC | 5607 |
rs184161212 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802783 | GGAGCTGCACCATGC[C/G]GCGCTTCCATTGTTC | 5607 |
rs184230001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725492 | TAGATCTTGACTATA[C/T]GTGTGGTGGGCAAGT | 5607 |
rs184239198 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766665 | AATAGGCAGGTTCTT[A/G]GAGATCTTTCACATC | 5607 |
rs184240945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665657 | AATGAGGGTATCTAG[A/G]TTTTGACAAATCAAA | 5607 |
rs184270055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770680 | TTGCTAACCAAAATC[A/G]TTGTGTGCCATCCCC | 5607 |
rs184272821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742688 | AGACCTCATACCATC[A/G]GGAAAAAGATTTTAT | 5607 |
rs184274497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721945 | ATCTTTAATTTGCAG[C/T]GTATTATGATATCAT | 5607 |
rs184278988 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787600 | TATTAATCATAAGAA[C/G]AGTTATTTAAAATTG | 5607 |
rs184300485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589681 | TTGCCTGGGCTTTGT[C/T]TGGTTATTTGCATCT | 5607 |
rs184306474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570406 | TGACCATATGTGGAC[C/T]CTCGGTCAAGTCTTT | 5607 |
rs184306712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550847 | TGCGATCTTAGCTCA[C/G]TGCAACCTCTGCCTC | 5607 |
rs184322407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648244 | TACTTTCTCTTTCCT[C/G]AAGTCCTTGGCAACC | 5607 |
rs184327445 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606029 | CTCTTTTTCTTGGGT[A/G]GTATGTCATATGGAA | 5607 |
rs184331112 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687332 | TATGCACAGCCAAGC[G/T]TAGGAGCTATTTATT | 5607 |
rs184335885 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667653 | CTTAAAAACCAGAGT[A/T]AAAAAAAAAAGAAAT | 5607 |
rs184338152 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629043 | TCTGGCCCCTATGGT[C/G]GTGGAGGCCAATACT | 5607 |
rs184338730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706475 | GCAGATAACCAGATG[A/G]TCAGGAGTGAGGGCC | 5607 |
rs184339171 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795360 | TTTCCTAATATATGC[C/T]TATAAAGCTATGAAC | 5607 |
rs184345501 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754369 | GAAGAAAAGAGAAGA[C/T]ACACTTAAACCACAT | 5607 |
rs184346487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593726 | GCCTATTAGGCTGTA[G/T]TGACTGAGACATCTG | 5607 |
rs184358934 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647596 | TACAAAAAAATTTTT[A/T]AAAATATGGCCGGGC | 5607 |
rs184362387 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669795 | GAAAAGAGATAACAA[A/C]AAAAAACCTGATAAT | 5607 |
rs184372617 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621062 | GTATTGGGAGAAAAT[C/T]TAAAATACCAAGACA | 5607 |
rs184401681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685994 | ATGACTCTTTACAGG[A/G]AAAGTTTGCCAACCT | 5607 |
rs184428978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575856 | TAGTTCTCTCCCTCT[A/G]TCTCTATCTCTCTAT | 5607 |
rs184434935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771572 | GTTTTCCCAAGAGAT[A/T]CAGCTACTTTGGAAT | 5607 |
rs184453869 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610805 | GCATTAAATTTTTTT[A/T]AAAAAACATTAATTT | 5607 |
rs184454356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652127 | TTAGTGATGTCAAAC[A/C]TTTTTTCAAATGCCT | 5607 |
rs184460376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632009 | AATCTGTTACTTCCC[A/G]TCATGCCCTTTATCT | 5607 |
rs184466236 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671753 | TGCCATGCTGGTGTG[C/T]TGCACCCATTAACTC | 5607 |
rs184475797 | snp | C/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547438 | ATCAAAATATGTAAA[C/G]TTCGGTTTTCTTTTT | 5607 |
rs184476424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710344 | ACCCCTCTTCATCAT[A/G]ACCAGTGTTTTATTG | 5607 |
rs184483196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691752 | TTCACAGAAATCCTT[C/T]GTGTCATTACTTAGC | 5607 |
rs184489070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552081 | TTGGGTTGGTGGGGG[C/T]GGGAGGGGGTGGATG | 5607 |
rs184526585 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715245 | GCGGGGAGGGGGGGG[G/T]TCTAAAATTGTGTGT | 5607 |
rs184538368 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772425 | AGTAGAATTAGGATA[C/T]ATTTAATTTAAATTC | 5607 |
rs184551950 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754831 | AAATGCATGCCAAAA[A/G]GCGTAGGTGTTACCC | 5607 |
rs184560595 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652595 | CTCTCACGAGGCCCC[A/G]TCTTCAACATTGGGA | 5607 |
rs184571699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693060 | TTACTCCCAGCCAAA[C/G]ACGAAGACCAAAGCG | 5607 |
rs184572949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759883 | TGTATTAGTTAATGA[A/C]TGAGGCATTAGAAAC | 5607 |
rs184574442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788516 | TAGTACCCACTGCAT[A/G]GAAAGGGGATAATAG | 5607 |
rs184582845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726681 | CTAGGCTTCCACTTA[C/T]TAACTGTTTGGGAGC | 5607 |
rs184593425 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793490 | CCTTTAACACACCTT[C/T]GTCTTCTCCTTCTAT | 5607 |
rs184599469 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745996 | TCTCTCTTTAAAAAC[C/T]TGGGCAAAACAGTAT | 5607 |
rs184607292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570847 | AGTATTGACAACAGG[A/T]ATTTGAAAATTTTAT | 5607 |
rs184642061 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617864 | CCCAGCTAATTTTTT[A/T]AAATTTTTTGTTGAG | 5607 |
rs184656341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558214 | TGAATCCCTACCATA[A/G]TGGTACCTGGCACGT | 5607 |
rs184656621 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551896 | TACGGAAAGATATCT[C/G]TGAAATATTGTTGAA | 5607 |
rs184666608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799510 | AGCTGCAGACAGCTG[C/T]CCTGTGTTCAAAACC | 5607 |
rs184670658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771827 | GCTTGTTAGAAGAGT[A/G]CCTTATAAAGAAAAA | 5607 |
rs184683151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789456 | GGCGTGGCGGCTTAA[C/T]GCCTGTAATCCCAGC | 5607 |
rs184688089 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673072 | TACTGTAGCCTTGTA[G/T]TATAGTTTGAAGTCA | 5607 |
rs184707650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736640 | CAATCACCATATAAT[A/G]TATAGAATTATATAC | 5607 |
rs184717253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711301 | TAAATGCCCGTAAGT[A/G]TTTGGAGAATAGATC | 5607 |
rs184720175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775532 | TTGTTAGTTGATATA[C/G]CATTGTGCACAGTCT | 5607 |
rs184740754 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759572 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 5607 |
rs184742154 | snp | A/G | 3.32392e-05 | 0.00407658 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600783 | TTAAACTTTCTATCC[A/G]CTTTTCCAAATACTG | 5607 |
rs184767628 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634072 | CAGTCCTTGTACACA[G/T]GAAAAGAATGTATAG | 5607 |
rs184769507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611406 | TTGCAGAGCACAACA[A/G]CTGGGGTAACTGACC | 5607 |
rs184774148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576257 | GTGCCTCATAAACTT[A/T]AACTGTGCTGTTTTG | 5607 |
rs184774299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654862 | GGTCAGGAGTTCAAG[A/G]TTAGCCTGGCCGAGT | 5607 |
rs184780451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594954 | GTTGTAGGCATCAAT[A/T]AATTTCTGGGCTGAA | 5607 |
rs184795686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736933 | TGATCTAGTCCAACT[C/T]TTAGATTACAGATGA | 5607 |
rs184800669 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760343 | AGTTATAAGAAAATT[G/T]TTTCCTCATAGTCTG | 5607 |
rs184801252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637105 | GGGGGCTTTCAGGCC[A/T]TCAGCTACAGACTGA | 5607 |
rs184802787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629262 | AGCTGCTACAAAGAA[A/G]ACATGTTTTAGACAA | 5607 |
rs184805105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776285 | CTGCTTTTAAATCAC[A/G]CTGCTGCAACTCCCA | 5607 |
rs184811452 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794378 | CAAAACAATCAGAAT[G/T]TTCGAAGAGTTTGCT | 5607 |
rs184811887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648025 | AGTCTAGGCAACAGA[A/G]TGAGACCCTGTATCA | 5607 |
rs184816091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604171 | TGAATTCTGTGTGCT[A/G]TCTCCTGACGAGCTG | 5607 |
rs184845969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682287 | AGTGGTGTGATCTCA[A/G]CTCACTGCAACCTCC | 5607 |
rs184857409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702445 | ATTGGGGTGTAAGTT[A/T]TGATCTCAGCCTTGC | 5607 |
rs184878174 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718580 | ACCAGCCTGGCCAAC[A/G]TGATGAATCCCCGTC | 5607 |
rs184905177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780023 | TGGTCCTCCTCCCTG[C/T]GGCTTTTCCCTACTC | 5607 |
rs184907743 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681082 | TTTTCCCATTCATCT[A/G]ATTCATTCAACATTT | 5607 |
rs184919225 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598846 | CAGAATTTGTGTACT[G/T]GAGTGAGTGAAATGT | 5607 |
rs184923543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616226 | GAATAGAAGCATCAT[C/T]TGTAAGTATAGAAAC | 5607 |
rs184927563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580886 | TTTCATCAACAGTTA[C/T]GTTTCCAAAGGTTTA | 5607 |
rs184928640 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676761 | GGTGAAGCAATCAAG[A/G/T]CTCAAGCAGCCTAAA | 5607 |
rs184933267 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622093 | GAGGTGGCAGTGAGC[C/T]GAGATCACGCCACTG | 5607 |
rs184957765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631446 | TCCTATGCACCTTTT[A/G]CTCTGCCACAGATTT | 5607 |
rs184958387 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714739 | GCCCAAAATTTGAAG[G/T]ACTCCCAAATTCGAA | 5607 |
rs184959097 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651451 | ATCACTCTGTTGTGG[C/T]GCCAAACACTGGATC | 5607 |
rs184989443 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562850 | CAGTAAGTGTTAGCC[A/G]TTTTTATCATGCTGT | 5607 |
rs185004369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559473 | TTTTGGATTGCATGT[A/T]GCCTCAAATAAAATT | 5607 |
rs185007843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764970 | AACTTTCTATTTTGA[C/T]GTAATTTTTAGATTT | 5607 |
rs185022874 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799761 | CACTCCCTCCCTGGG[C/G]ACAAGGCTCAGGAGT | 5607 |
rs185037990 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635186 | TTGCTTTAGATATTT[A/T]TCTTTTTTTTTTTTT | 5607 |
rs185044023 | snp | C/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654951 | ATGCCTGTAATCCCA[C/G]CTACTCGGGAGGCTG | 5607 |
rs185046275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697126 | ATGGGTGAGGGTGAA[A/G]AAGTGGGGAAGAGGA | 5607 |
rs185077723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732073 | GCATATTCTGCAATA[A/G]GATAATGAAAAATTG | 5607 |
rs185154775 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686636 | TAATAATAATAATAA[G/T]AATAATAACATGTTG | 5607 |
rs185155732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600325 | TGTCTTCCTAAGTTT[A/G]ACTTTGGTTATGTGC | 5607 |
rs185159013 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691652 | TGCTCTATACCATCA[A/G]AAGTGGTATGCTCTT | 5607 |
rs185162701 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599701 | TTTTTTTTTTTTTCA[G/T]GGCTTGCAGTGGCTT | 5607 |
rs185166397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563045 | TAACCTAGAGATATG[C/T]TGTGAATGACATGAG | 5607 |
rs185172463 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777750 | AATTGTTTAAAAACA[C/T]GGGTTTTCTCCTTAG | 5607 |
rs185173123 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605944 | GAGGAGATTGATATT[C/T]GAATGATTAACTTTC | 5607 |
rs185180511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796377 | GAAGCATGGCTCAGG[A/G]CATCTGCTCAGCTTC | 5607 |
rs185190142 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681364 | GTACACACACCCACA[C/T]GTACATGTATGCTCA | 5607 |
rs185202289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616927 | CCTCTTTTCACTAAC[C/T]TTCTTTGAAGTACGT | 5607 |
rs185225856 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702912 | GTTCCAGACCAATCT[A/G]TCAAAATGCAAATAA | 5607 |
rs185238816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767143 | TAGTCTTATAATATG[A/G]GGAACTTAACAGGCT | 5607 |
rs185244855 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737286 | AGCAGCAACAGACAA[A/G]GACATCAACTTTTAT | 5607 |
rs185258856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803801 | AGGCAGGCCTGAGTC[A/G]CCAAGGTAGAAACAA | 5607 |
rs185269154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776969 | CCCAGAAATTACATC[C/T]GAAGTTATCTATGCA | 5607 |
rs185271288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546069 | ATGTTTTGTCAGAAA[G/T]GCCTGACGAAGGACC | 5607 |
rs185282047 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581249 | AGAGAAATTTTGGTG[A/G]AATGTTTGGTATCTG | 5607 |
rs185297873 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585047 | TGTTGTCAGAAACAG[A/G]AAAACGACATGTACA | 5607 |
rs185315455 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765433 | ATACAAGACACAAAC[C/G]ACTGATCTTATTCAG | 5607 |
rs185321043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581746 | GCTCAATTAACCAGT[A/T]GGCTCCTATTTGCAC | 5607 |
rs185323579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780534 | AGACAAACAAGACAT[A/G]TATCTGGTTCTCCAG | 5607 |
rs185331041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800043 | TGTTGATTAGCCTGG[C/T]CACGCCCAGCCTGGA | 5607 |
rs185333596 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563151 | AAACAACAAACTAAT[A/T]ATGTCAACATACCCC | 5607 |
rs185349703 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719198 | TCATCATAATGGTTA[A/C]ATATGTGAAAATGGT | 5607 |
rs185363613 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639814 | CACTTCAACACTTTG[A/T]TTCACGTATTCCTCT | 5607 |
rs185363900 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717769 | CCAGGAGTGGCTGGG[A/G]CCCTCCTCTCCCATC | 5607 |
rs185367829 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783431 | CTTTGCTTGTGCTGT[G/T]TTCTCACCGCCAGAT | 5607 |
rs185370448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786395 | ATGAGCATCTTGTTG[A/G]AGGGAATTATTGTAA | 5607 |
rs185374332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760953 | CTGTAATCGTTTTGC[C/T]GGCTGTTAATTTTCT | 5607 |
rs185376491 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686471 | AACTAGCTGGGGGTG[A/G]TGGCAGGCGCCTGTA | 5607 |
rs185377252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805804 | TGAAGAGGAAGAAAA[A/G]GAAGGCTTTTCACTT | 5607 |
rs185377715 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658572 | ATCTTTGGATGTATA[C/T]AGGAAAATGCCAGAA | 5607 |
rs185379467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623691 | TAACCTCCACCTCCT[A/G]GGTTCAAATGATTCT | 5607 |
rs185383025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721264 | ATGCAGAACCTTCTG[A/G]ATGGTAGATAAGTGC | 5607 |
rs185386654 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806275 | CGGAAAGCTGGCAAC[A/G]CAGTGCCAGGCCTCG | 5607 |
rs185389224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722628 | AGTTTCAGATGATTT[A/G]AACTCTTTCTCTAGG | 5607 |
rs185395563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680441 | TTTTACCATTGGTAT[A/G]TATTATATGATTAGT | 5607 |
rs185401331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743226 | CAGAGAGAAGGTGCC[A/G]GTGAGTAGATCTTAG | 5607 |
rs185402919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764562 | TCTTATCCCTCTGAA[C/T]AATACACAAATTCTT | 5607 |
rs185403422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716244 | TACTCGGGAGGCTGA[C/G]GCAGGAGGATCCCTT | 5607 |
rs185405221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699115 | AACTCTTCTGTTTAA[A/G]TATGCTAGCTAAGTT | 5607 |
rs185417565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603304 | TAATTAGGGCTACTA[C/T]GTCAAAGGGACCATT | 5607 |
rs185423690 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621252 | CACAAATACCATGTA[A/T]TAATATGAAAACTCC | 5607 |
rs185428212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565556 | ATTAAATTCTGAATA[A/G]TTTGGGTTTATATAA | 5607 |
rs185463388 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769989 | CCCCTACTGAACGGA[C/T]GTACGAAGCTTATTT | 5607 |
rs185508818 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706018 | TAGGTATTACTCTTA[C/G]AAGAAATGATCTGAC | 5607 |
rs185520795 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662015 | CTGTATTGTCTTCCT[C/G]TCCAGAATACATGTG | 5607 |
rs185525292 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741736 | CCAACTGATCATAAG[A/G]AAGAAAACAGGGATG | 5607 |
rs185526772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626536 | CATCTTAAACAAGCA[A/G]ACAAACAAAAAACAT | 5607 |
rs185528825 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644318 | AGAATGGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 5607 |
rs185537114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683711 | GTGGCAGTGAGCCGA[A/G]ATCGCGCCATTGCAC | 5607 |
rs185539832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636697 | GGGTGCTATTTTTGC[C/T]CTGCTATAAATATTT | 5607 |
rs185553416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703140 | ATTCAGTAAGAATAT[A/G]TCTATATATAATTTC | 5607 |
rs185555487 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802725 | GGTCACCGTGGGTGG[A/G]AGATGCTCTTGACAA | 5607 |
rs185564752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571932 | TTCATGCCCTCCAGG[A/G]GCTCATGGTCCAGTC | 5607 |
rs185575280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666312 | TTATCTTGATTTTTC[G/T]TCTTTAAAATTAGAA | 5607 |
rs185581221 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607703 | TTTTGAAAGACACTA[A/C]ATTTCATTTTTAAAA | 5607 |
rs185590928 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609244 | ATTTTTCACTGAACA[C/T]CCTGTCACTGTGCCA | 5607 |
rs185593581 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671019 | TCTGACATTCCCAAT[G/T]CAGTCCTACTGACTG | 5607 |
rs185615174 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772996 | CTCATCAAGGGTCAC[A/C]AACTTAATGTAGGTT | 5607 |
rs185662398 | snp | A/C | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719916 | TCAGTGCACAGAATA[A/C]CATGGAAAAAGACCT | 5607 |
rs185680560 | snp | C/T | 0.145305 | 0.227022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592817 | GAAGGATGTGAAGAA[C/T]ATGCTCAATCCCTAT | 5607 |
rs185693982 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552363 | TTCGGAGTACTTACT[A/G]TTGACAGATGCTTTG | 5607 |
rs185710247 | snp | A/G | 7.16025e-05 | 0.00598298 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642544 | AGCTGGGTCTAAAAG[A/G]TAGAACAGGTTTTTT | 5607 |
rs185721838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745107 | TAGAGACTGATTAAC[A/G]AAGTGTGTGACTGGA | 5607 |
rs185722092 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791268 | TGGAGTTGAGGGATG[A/G]GGCAAAGACTGAAGG | 5607 |
rs185722881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625564 | ACTTTACAATTAATG[C/T]GTTGAGGAAGGTCAA | 5607 |
rs185725405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766210 | TGTGTCCCTTCAGCA[A/G]AACTCTAAAGTTGAT | 5607 |
rs185726427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710101 | TCCTGGGTTCAAGCG[A/G]TCCTCCCTCCTCAGC | 5607 |
rs185727253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590519 | TGCTGTCACCCCCCC[A/T]TTCTGGAGTGCACAA | 5607 |
rs185735146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567817 | TCTCATTTCCTCCTC[C/T]CATTTTCTAGAAAGA | 5607 |
rs185735161 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549041 | TGCTTGGAAAGGCTG[A/T]GGGCTCCCTGCTGAG | 5607 |
rs185836282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690166 | AAAGAACAAATTGTC[C/T]AAAAGAAAAATATTT | 5607 |
rs185852252 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605103 | CTGTCGCCAGGCTGG[A/G]GTGCAGTGGAAAGAT | 5607 |
rs185859101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660579 | AGGGTGCCATTGCCA[A/G]GTCAAAAGCAACAGA | 5607 |
rs185862023 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595998 | TTTTTTTGTTTTTTA[G/T]ATTTTATAGGAGAGG | 5607 |
rs185866791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749485 | AGGAAAGTTTGAAAG[A/C]AAAAAATTGTAATTC | 5607 |
rs185869115 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587998 | ACTCCCTCCGTTCTT[G/T]GCCCATTCAGCCCCT | 5607 |
rs185869295 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629381 | AAGCATTCCAACAAA[A/G]TGATCTAATGTAGAT | 5607 |
rs185882452 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629809 | TATTAATATTTTTAT[G/T]GGCTTGCAATAACAA | 5607 |
rs185882895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769296 | TGTGTGTTACTTAAA[G/T]AATCATTAATTTCTC | 5607 |
rs185885596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623080 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 5607 |
rs185886961 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785240 | GTGAGCCACCGTGCC[C/G]GGCCCCGAACTGTTT | 5607 |
rs185919160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653811 | TCTTATTTAATGTAG[G/T]TTATAAATTTTCCTC | 5607 |
rs185931646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674718 | CTTTTAAAAGAATAT[A/G]TGCCTAGAATATATA | 5607 |
rs185934314 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804877 | TGGGAAAGCAGCCGT[G/T]GGGTGGGCATATATA | 5607 |
rs185944828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712348 | CTTAGTCTACAAGCC[C/G]CATCCATGAGCACAG | 5607 |
rs185945007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694492 | AGATTTAGGGATGGA[A/G]AAAACACATGAAAAA | 5607 |
rs185960941 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728629 | AAATGAATGGTTTGA[C/T]TGTTTTCCTCTGGTT | 5607 |
rs185966417 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735101 | ACTTATACACATTTG[C/T]TTCTTCCTAGGAATT | 5607 |
rs185976724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774318 | ACAATGAAAAATGTT[A/G]TCACAGGAAGCACCA | 5607 |
rs185988790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578019 | AAAAAGAAAACCCCA[A/G]TTTGTTTTGCAGTTT | 5607 |
rs185999827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608668 | TTCTCTGAGAAAGAG[A/G]AGATTAAAGGGCTCC | 5607 |
rs186009220 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668561 | AAACATACATCGCCA[C/T]TAATGAGGTGAGAGC | 5607 |
rs186014659 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573663 | GCATTCTTAGTTACA[A/G]GATGTTTAGAGTTAA | 5607 |
rs186016868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591057 | GTGGATAGGTTAAGA[A/G]TAGAGTTGGCTGGGT | 5607 |
rs186021755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706957 | GTCTTGCTCTGTCGC[C/T]CAGGCTGCAGTGCAG | 5607 |
rs186024969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648806 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCT | 5607 |
rs186025258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614475 | CTAGTCAATCCTCAG[A/G]GTATTTCTATTTTCC | 5607 |
rs186034914 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626295 | TGGGAGGCCGAGGCT[C/G]GTAGATCACTTGAGG | 5607 |
rs186068998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630094 | AAAAGTAAAAAGTAG[C/G]ATGGTGGCATGTGCC | 5607 |
rs186079236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596160 | TGTATTTGGCTGGGC[A/G]TGGTGGCTCATGCCT | 5607 |
rs186079475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678250 | AAGATCCCAGGCACA[A/G]TGCTAGGAGAGGTTG | 5607 |
rs186082087 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553303 | CCCCAAGTGTGTCAA[A/C]AGCCTGTTAAGTGTA | 5607 |
rs186085504 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615054 | CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTTGGC | 5607 |
rs186087065 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669171 | GCTTTCACAGTACTT[A/G]AAACACATCAATATG | 5607 |
rs186095117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698156 | GGGTCTGGAAACTTG[A/G]AGCTTATATTAAATT | 5607 |
rs186095161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649333 | TTTCACTTATTGTTT[A/G]TCTTTTCACTTTCTT | 5607 |
rs186098900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757445 | TTTGGTTTGGTCAGA[A/G]TATGGGAGATTCAGA | 5607 |
rs186105156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715432 | ACTGGCAGACAAAGT[A/G]AAGTGTTTCCCACTG | 5607 |
rs186107179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733784 | ATAGGTAGATAATAA[A/G]TGAAAAATATGCATT | 5607 |
rs186118643 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791635 | TGACATCCAGTGCAA[A/C]TCCCAGCTCTACCTT | 5607 |
rs186134592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579482 | TGTTTCACATGTTTA[G/T]GCCGTATGTATATAA | 5607 |
rs186148732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560198 | CTTTAGAGAGAAGTG[C/T]ATTTTTGCTTTACAG | 5607 |
rs186159963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687706 | GATGGAGCTCCTTCT[C/T]AGGCCAAATTCATGC | 5607 |
rs186178745 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636571 | TCTTATAATTTTTTT[A/T]AAGTGAAAAGCAAGT | 5607 |
rs186206542 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554289 | GTCTTGAACTCCTGG[G/T]CTCAAGCAATCCATG | 5607 |
rs186219168 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755272 | TGTGAGCCACCACTC[C/G]TGGCTTTTAGAAGCT | 5607 |
rs186233252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591877 | AGCACTTTGGGAGGC[C/G]GAGGCGGGCAGATCA | 5607 |
rs186290970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582104 | GTCTCGCTCTGCCAC[C/T]AGGCTGGAGTGCAGT | 5607 |
rs186308983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695623 | TGGGGGGACATGACT[A/G]TAAATGAAACAATTG | 5607 |
rs186318913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761316 | ACTGGTGTAGTGTCT[C/T]CTTAAACCAGCTTTA | 5607 |
rs186331495 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729632 | AAAAAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 5607 |
rs186335031 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795652 | ATTTGGTTTTTCCCC[A/C]CAGTGTTCTCTCTTT | 5607 |
rs186391288 | snp | A/T | 0.299411 | 0.245069 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576934 | TATATATATATTTTT[A/T]TTTTTTTTTTTTGAG | 5607 |
rs186405611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573975 | TGCTTTTGGGAACAC[C/T]CAGCTCTGACTGGGT | 5607 |
rs186417605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619338 | TTGTATATTTATTTG[A/G]TTATTGTCAGTCAGC | 5607 |
rs186422383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635071 | AGTCTACAAATCTTA[C/T]AGTGGTGTATTTTCA | 5607 |
rs186425057 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786033 | GTTTTTTTTTTTTTA[A/T]CTTACAGAAGATGGA | 5607 |
rs186426603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601452 | TATGAAAAATATTCC[A/T]CTAGGAATTAAAAAA | 5607 |
rs186439729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653270 | GCTAAAAGTTTGTCA[G/T]TTTCTCTGTTTAAAA | 5607 |
rs186446065 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711990 | ACCCAATAGAAAACA[A/G]TTGTTAATGTACTGG | 5607 |
rs186454363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674046 | TAGAGACAGGGTTTC[A/T]CCATGTTAGCCAGGC | 5607 |
rs186462680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799066 | CCCAGCTACTCAGGA[G/T]GCTGAGGCAGGAGAA | 5607 |
rs186467766 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599684 | AATTCCCTGGAAATT[G/T]ATTTTTTTTTTTTTC | 5607 |
rs186477885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679996 | GCTCCTGTCCTCAGC[C/G]CCAGGGAACCACTGA | 5607 |
rs186486828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738053 | GATGAGATTTCGCCA[C/T]GTTGGCCAGGCTGGT | 5607 |
rs186487422 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715845 | TTCAGTATAAAGAAG[C/G]ATTTTCTGATGGATA | 5607 |
rs186492825 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756029 | CAGCTACAAACCTAA[C/T]GGAGAAAGCCAGCAT | 5607 |
rs186511391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712896 | GCACTCCGCCTGGGC[A/G]ACAGAGCAGGCTGTC | 5607 |
rs186513155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613411 | ATTCGGTCAGAGAGA[C/T]TACCTATTGTATAAT | 5607 |
rs186514828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777460 | TGGCTAATACTTTAT[C/G]TAGGCCACTTTATTA | 5607 |
rs186528878 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703422 | AGGTACGTTGTTTGC[A/G]CATAGACGCTTCTGT | 5607 |
rs186533878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639413 | AATGCTCACAACATT[C/T]TGTAACTCTTACTGA | 5607 |
rs186534583 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751936 | CTGTACTGCTCTGCA[G/T]AGTGCTTTTCCTGTG | 5607 |
rs186543004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720237 | TAATATACACATACA[C/G]AAACATAAACACACG | 5607 |
rs186547332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738469 | AGCAAATGACACACC[C/T]GACAAGTGACAAATT | 5607 |
rs186550903 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761871 | ACTTCTGTAGAACCA[A/G]CTGAAATGCCAGTGT | 5607 |
rs186557206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558832 | TCTCTTTCCACTAGA[A/G]TGTATGTTCCATGAA | 5607 |
rs186565532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764426 | TCGTTTGTGAACTCG[C/T]GTCTGCCAGCCAAAC | 5607 |
rs186567423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779534 | GTCTTTATATGCATG[C/T]GCATAGCAAGAGAGA | 5607 |
rs186580607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595552 | TCTTCTTAACACAGA[C/T]AATAAACAAAGAATA | 5607 |
rs186610550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781418 | TTGTGGTTTCGGATA[C/T]AGAGTTATTTGGGGG | 5607 |
rs186649834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564104 | TACAAAACCTTTTCC[C/T]GTGGCCTGGTAGAAA | 5607 |
rs186664990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698571 | CTATTCAGTCTTCCT[G/T]GCTTACTATCATTTT | 5607 |
rs186686966 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745636 | ATTAAATTTTCTGGT[A/G]GAATTAACAGAGGAA | 5607 |
rs186691778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766594 | TGAGCTACAGTGAAA[C/G]TGGAGCGCAAATTTA | 5607 |
rs186691993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718360 | GTCAGCGTTACACAA[A/T]CTTTTTAAAAGGGTG | 5607 |
rs186692715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661015 | TCTTTTCCCAAATTA[A/G]CTTTATTTTCCAGGG | 5607 |
rs186695267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782462 | CCCTGTGATATACTG[A/G]AAGGCTAAATATTTC | 5607 |
rs186695953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736730 | TAATCAATTTAGCCC[A/C]CAGAAATAGAATTGA | 5607 |
rs186698926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602006 | AGTTCTTCCACTATG[A/G]TAATTCAGAGAAATA | 5607 |
rs186700936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734632 | ATGTCTTATATTCTA[C/T]GTTAAATTTAGACCA | 5607 |
rs186721607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562751 | ATAATAATAATGATG[C/T]TCATGTCGCAGGTTT | 5607 |
rs186727915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605561 | TCCTAATTTATTTTC[A/G]GATTGCTATAGGACA | 5607 |
rs186758499 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657669 | AAAGTTTAACTAAGA[A/G]TGATCATTTTTCTCT | 5607 |
rs186787785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805304 | CTAGGATGAGGCGGC[C/T]TGAGCATTCTCCTGT | 5607 |
rs186794463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802537 | AGTTTAATTGTTGCA[A/G]TTGGCCCTCAGAGAA | 5607 |
rs186817462 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635216 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCTAGG | 5607 |
rs186845235 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660871 | TTCCTAACAGAATGA[A/G]AAAAAAAAAAAATAG | 5607 |
rs186849708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802318 | TTCATCTTCATGACT[A/G]TGATATTTTCACCAA | 5607 |
rs186856035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628842 | GAAACTTCAGTGGTC[A/T]TGGTGGCTTTGATGG | 5607 |
rs186859460 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580520 | ACTAATATAAAGTCT[C/T]AATCAACACTTTTAC | 5607 |
rs186861263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598269 | AGGCCAAAGGTTTGC[A/G]TAACTTTAAAACATT | 5607 |
rs186880896 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805604 | GAGGGAGGAGAGAGC[G/T]GGGGGGAGCGAGGAA | 5607 |
rs186881990 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541437 | AAAGAAATAAAGGAC[G/T]AACCTACACATTACA | 5607 |
rs186891823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620269 | CCAGCTATTCGGGAG[A/G]CTGAGGCAGGAGAAT | 5607 |
rs186908077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583526 | TTGGTAGTCTTTTGC[C/T]TTTTGCTACCTGTCT | 5607 |
rs186969182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647433 | TCTTTGAAGTCTTCA[A/G]TTTTTCAGTTCTACT | 5607 |
rs186974458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685254 | ATAAGATTGACAGCC[A/G]ACTTCATGTCACAAG | 5607 |
rs186985828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602572 | AGAAGCATAAGACCA[C/T]GAAACCCCAGCAGAA | 5607 |
rs186987469 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664941 | TAACTATTGTTAATG[C/G/T]AAAACCTTTGCTTTC | 5607 |
rs186989021 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704833 | TATTTTAAATTGTTA[A/T]CATTTATTTTATAAA | 5607 |
rs186992956 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584588 | ATATTTTCTAGGAAA[A/C]ATAACATAATAAATT | 5607 |
rs187001645 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656932 | AGAAAAAGAACTCAT[A/C]AAACTTAACAGGAAC | 5607 |
rs187013086 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688391 | CAAACTATAATAGAG[A/C]AAGTGTAAAACTAGG | 5607 |
rs187013123 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740679 | CTTTCAGTAAGATTT[A/G]TATACTTCTCGGTCT | 5607 |
rs187014785 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720702 | GCCTTGCAGAGCGCT[A/G]TCAATCACTCAGTGA | 5607 |
rs187015565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797698 | CATTGGTTCTTTTTT[G/T]TTGAGACAGAGTCTC | 5607 |
rs187023952 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645734 | TTTTTTTTTTTTTTT[G/T]TAGAGATGGGTTCTC | 5607 |
rs187024279 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683034 | TAATCTCAGAGACTC[A/G]GGAGGCTGAGGAAGG | 5607 |
rs187051167 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769107 | GCCTTTCTATTAAAG[A/T]AAAAAAAAAAAATTG | 5607 |
rs187059834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543950 | GGGCCTCACTCTGTC[A/G]CTCAGGCTGCAGTGC | 5607 |
rs187060927 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564564 | GATGATTAACAGAGC[A/G]TTGCATTCCAACCAG | 5607 |
rs187069207 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622798 | GTTTAACTTTATAGC[A/G]TTTATAAGAAAGTGT | 5607 |
rs187084068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587552 | ACTGAACATCCCTGT[C/T]GGAGGAATGCACTTT | 5607 |
rs187103325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625189 | CTATTGTTACAAATG[A/C]AATAAGAAAGTATGG | 5607 |
rs187105242 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650258 | ATACAAGATAATGCC[A/G]TCTGCAAATAGAGGT | 5607 |
rs187109782 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787820 | TTGACCTAACTGTAG[G/T]CTTTAACTGCATTGT | 5607 |
rs187110449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641290 | TTAAATGGACCATTT[C/G]ATTAATCATTTGTAT | 5607 |
rs187115893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606437 | GTATATATACTGCCT[C/T]CATGGTGTTTTGAAG | 5607 |
rs187118070 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669526 | GGCCAGTGTGTCTGT[A/G]TCTGAGTGTGGGAGA | 5607 |
rs187139972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708404 | TAGCACCCTTTCCTC[C/T]AGTTCCATAAACTGT | 5607 |
rs187144875 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689696 | GGTTCTTATTTACAC[A/C/T]TTGTCTTTTGGAATA | 5607 |
rs187156180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724370 | ACTTTTGACAGCCTC[G/T]TGGAGAACTCGTTCT | 5607 |
rs187163804 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765888 | GCATTCTGAACTTGT[A/C]CTTTTGCTCATAGAT | 5607 |
rs187180666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801955 | TCAAAGCCCAACTAA[A/G]GGCAGACAGCGAGGT | 5607 |
rs187180785 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589728 | TATCAACTGGGAGTC[A/G]TTTGTGGGAAAACTA | 5607 |
rs187191651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551470 | CCCAAGTAACTGGGA[C/T]TACACGCATGCACCA | 5607 |
rs187204193 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638857 | CATAGGATTGTTGGC[C/G]TCGTGTATATCTTCT | 5607 |
rs187242551 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567451 | CTCACTGCAAGCTCC[A/G]CTTCCCGGGTTCACG | 5607 |
rs187269801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604724 | ACATAGTGAAACCCC[A/G]ACTCTACTAAAAATA | 5607 |
rs187283169 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571166 | ATTTCTCAGGTTTTT[G/T]AAGGCATAGTCCTTT | 5607 |
rs187305408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574739 | GGGCGTGGTGTCGGG[C/T]GCCTGTAGTCCCAGC | 5607 |
rs187310418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593342 | TTTCTCACCTTAGCT[C/T]CTTCTTTTGTCCTGA | 5607 |
rs187313569 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556284 | TCTCTTCTTTTTTCC[A/G]TGGAGAAGTTTAAAA | 5607 |
rs187314264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712022 | GTAAACACCATGGGT[A/G]GACACTCAATCTAAC | 5607 |
rs187329496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748662 | TGGTGTGGAAAGCTT[A/G]TATTTTGTTTCCTAA | 5607 |
rs187329908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683735 | ATTGCACTTTAGCCT[C/G]GGTGACATGAGCAAG | 5607 |
rs187345940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707775 | GAAAGAGGGAAAAGA[C/T]AGAGGATCTCTTCCC | 5607 |
rs187363563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743689 | TTGTTTTTGCAAGTT[A/G]TAATGGATTGGAGGT | 5607 |
rs187375387 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780946 | CTCAAGCAAGTAACT[A/C]CACATCCAGAGGTTA | 5607 |
rs187390914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574464 | GTAGTATCAGCTACT[C/T]GGGAGGCTGAGGCAG | 5607 |
rs187414433 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645393 | TGAGGTGGGAGGTTT[G/T]TTTAAGTCTGGGAGG | 5607 |
rs187414747 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609560 | CTATAGGTCTGTAGA[A/T]TCTGTAGACCTATTC | 5607 |
rs187424417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628634 | TAACCTTTGACGACC[A/G]TGACTCTGTGGATAA | 5607 |
rs187425762 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793166 | TTACTTCCAGCTACT[C/T]GGGAAACTGAAACAG | 5607 |
rs187451084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646996 | TTCTATTTTGGTAGT[A/T]CTTTCTTGACCTGAA | 5607 |
rs187481505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686081 | CCCAAAAGAAAGCAG[A/G]AAAAGAAGAGAAAAA | 5607 |
rs187487352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720941 | GACCTCAATGTATCA[C/T]GCTTTTCAGCATTCA | 5607 |
rs187489414 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752784 | TCAAAATTGATCTAC[A/G]GATTCAATGTAATCA | 5607 |
rs187502487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786869 | GTAACCATTTTTATC[A/G]TCATTGTCATCATCA | 5607 |
rs187518804 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676412 | TTGTTCCCCTTTCTC[A/G]TATTAAAGTAAGAGA | 5607 |
rs187532902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696477 | AAAAGTTTGCCAGCC[C/T]CTGATCTATGCCAGT | 5607 |
rs187539088 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714475 | CACCCTGACACAGCT[G/T]TTTCTAATGGGTGTG | 5607 |
rs187540672 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731472 | TTCCTTTAGGCCTTT[G/T]GGTTGCATAACTTCC | 5607 |
rs187545113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754082 | TATGAAATGTCCACA[A/G]TAGGGAAGTCTATAG | 5607 |
rs187550728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569047 | ACAAAACTCTGTGGG[C/T]GTCTGAAGGTTTAAA | 5607 |
rs187552645 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751080 | CCACTAAGGTGGGCA[A/G]GAGCCAGTCCTGGAA | 5607 |
rs187559636 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596113 | TTTGGCTGTTATTTT[G/T]ATAACTTCAAAAAGC | 5607 |
rs187580404 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662891 | TGGCTTATGAGGACC[A/G]TCTTGATATACTTCA | 5607 |
rs187590404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728042 | GAGCCACATACAAAT[A/C]AATCTGTCCTGTTAA | 5607 |
rs187608877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709724 | ATTTGAGTTCACAAC[A/G]TAAATCTGTAGTTGG | 5607 |
rs187612748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768495 | GCGCTGGAAGGTTGT[A/G]TGTAATGATATATTG | 5607 |
rs187641057 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592288 | TTATTTGTAAAAACA[A/C]ACCTGCTATGGACAA | 5607 |
rs187651302 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762565 | CTTTTAAATGACAGA[A/C]AAAAAAAAAAAAAAA | 5607 |
rs187669046 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693328 | GCTGTGCTTGTTTAA[A/G]CTGGAAATCACATTC | 5607 |
rs187673522 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670156 | ATGGGTGAATATCAG[A/T]TACTTCATGTTAAAT | 5607 |
rs187675777 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542891 | GCCCTGGGGCTCTTT[C/T]TTAATAGCCCCGGAC | 5607 |
rs187707430 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686633 | TAATAATAATAATAA[C/T]AATAATAATAACATG | 5607 |
rs187729647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730647 | TCTCATCCTAAGTGT[A/C]ACTCACTAGTCTGAT | 5607 |
rs187732732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705691 | TGGTGAGCCAAGATC[A/G]TGCCATTGTGCTCCA | 5607 |
rs187741731 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775809 | GGATGGGCAAAGCAT[A/G]AGTGTATCTCGGTTT | 5607 |
rs187748613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770273 | ATATCTGAAGAAACA[A/G]GCATTTTACTGCCAA | 5607 |
rs187760642 | snp | C/G | 0.00180541 | 0.0299908 | missense | MAP2K5 | GRCh38.p7 | 15:67806736 | GAGAGGCGGAGCCAG[C/G]AGGGGCCCCCGTGAG | 5607 |
rs187768739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549406 | TTGATAAGAACTGTT[C/T]GTGTTAAATGTGGCA | 5607 |
rs187796493 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620714 | AAGGGCTTGATTGAA[A/G]TTAAAACATTCTAAG | 5607 |
rs187801319 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556742 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 5607 |
rs187801729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775056 | AATGTAGGACTGGTG[A/G]GCTAGATCACCCTTA | 5607 |
rs187809350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792544 | ACTCACTCTCTGACC[A/G]TCTCTCTGGCTCATT | 5607 |
rs187813201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588920 | TCCTGGGCTCAAGTG[A/G]TCCTTCCACCTCAGC | 5607 |
rs187815087 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714508 | GTTGTGGCTTTGTTT[G/T]CTTTTCTAGCCCTTG | 5607 |
rs187820364 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593704 | CCTGTCCATTGCGAT[C/T]AAGCCTGCCTATTAG | 5607 |
rs187831049 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654280 | TTATCATTAGAAAAT[G/T]TCTTTGTCTCTAGTA | 5607 |
rs187860455 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616379 | TGCGTTTTAGACAAT[A/G]ATTTATTTGTCTTGT | 5607 |
rs187860599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699575 | CCTAGGTTGGACAAG[A/G]CACATCATGCTGAGA | 5607 |
rs187866747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631755 | TCTGCCACTGCTGGC[A/G]CTTGATCTTCCCATC | 5607 |
rs187875103 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690886 | TTAATCAGTGAGCAA[G/T]ATACTGTGCTTGGAA | 5607 |
rs187876883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735475 | ATTTGTCACTGAGCA[C/T]CTACTCTGTGCCTGA | 5607 |
rs187877240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689855 | CAGGAGTTCAAAATA[C/T]TTGTTCATTAACTGT | 5607 |
rs187879198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716560 | AGAAAATTCTCTTAT[A/G]TGCCTTATGTTGTAT | 5607 |
rs187879244 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671435 | CTGAAGATAAGAGAC[C/T]AAAGTATAAAACAAA | 5607 |
rs187882343 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766159 | ATGGCAGCTGTTTTT[A/T]CATAACAGTTGCCTG | 5607 |
rs187887011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725054 | GTTCCACAAGATGTC[A/G]GGAAATAACACTGAA | 5607 |
rs187896171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758719 | AATTCAGAAGTCTAA[G/T]CCTTAACCTTTGTGG | 5607 |
rs187907543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798307 | ACTGTACAGCCTGCC[A/C]AGTCCTATCCAAGGC | 5607 |
rs187924907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615608 | CCATTAGTCCTAAAC[A/G]TGTTAATAAAATCTA | 5607 |
rs187967165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651309 | ACACAAGCATACAAT[G/T]TGTAGTAATCAACTC | 5607 |
rs188004955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621093 | CAGCAAAATTGAAAG[G/T]AAAAGGGTAGGGGAA | 5607 |
rs188005119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655516 | TTGGTTTATAATCTT[C/T]TTCTTTCATGTTCAA | 5607 |
rs188010712 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654754 | GTTCAGATTAACACT[A/G]ACTTTATTTTAATAG | 5607 |
rs188015477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638580 | TATATTCATTTGGGT[A/G]TATACCCAGTAATGG | 5607 |
rs188017879 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760122 | ATTGAAAATAGGTTA[A/G]CATTAAGGCCAGGAT | 5607 |
rs188020490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695862 | TGACAAAACTAAAAT[G/T]GCTTTGCTTCTTAGG | 5607 |
rs188022669 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675966 | TGCAAATGGAAGAGG[A/T]TAGTTATTTCCCCAG | 5607 |
rs188024925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678084 | CCGTTGTGCACAGAT[A/G]AATTTGTAATGCAGA | 5607 |
rs188031335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715311 | GGCAGATGATGGATT[A/G]ACTAGTTCAGTCCTT | 5607 |
rs188035177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698065 | TAATTAATAGGTTCA[A/G]TAGATACCTTCATCC | 5607 |
rs188038415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793701 | GTCTATAGATTGTAA[A/G]GTGCCCCTAGATTTG | 5607 |
rs188053354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733536 | CCATCATCTGGCCAA[A/G]TAGAATAATTTGGAC | 5607 |
rs188068874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602971 | TTATTTTTTAAAAGA[A/G]GGAGTATACAGAGAA | 5607 |
rs188072116 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678981 | AAAAAAAAAAAAAAA[A/G]AACTAATCTTACAAG | 5607 |
rs188074187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574920 | TTTAGTGGTTAAATA[C/T]GGGGGAGAAGAGAAG | 5607 |
rs188085070 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584815 | CATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG | 5607 |
rs188091957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610190 | AGATATAAAATTAGT[A/G]TATAAATTTGAAAGT | 5607 |
rs188102539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675482 | AATGGAGCAAGATGA[A/G]GAATCCTCATGGTGA | 5607 |
rs188106605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635335 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTTTCT | 5607 |
rs188119245 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765737 | CTTGTCTCCTCCACC[A/G]GCTCTTTGAGTGTGC | 5607 |
rs188122783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681347 | GCATGTGAGTGTTGT[A/G]AGTACACACACCCAC | 5607 |
rs188125082 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780727 | GTGCCAAAATAATAA[A/G]ATTTCTAGGATGTTC | 5607 |
rs188133731 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800151 | CACTTGTCAGCAATT[C/T]AGCAGACAGTGGAAA | 5607 |
rs188136765 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580172 | CAGTGCAATTTGATC[C/T]GTACTAAAGTGTTTA | 5607 |
rs188155896 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660529 | GGCATCAACATCTTT[C/G]CCTTGAGTTCCCTCA | 5607 |
rs188171346 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642339 | TGGAGTGCTGGGGGG[A/G]ATAGAAAAATGTACA | 5607 |
rs188173148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601297 | AGTTGCAGTGATCTT[A/G]CCCCAAAGGAATGTT | 5607 |
rs188173356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681860 | TATTCATTTGAGCTC[C/T]CTTGCCTTCAATAAA | 5607 |
rs188180772 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618142 | TCATCTTTAACATTT[A/C]AAGGAGTAAATAATA | 5607 |
rs188182215 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778806 | CCGGGGCTTACCTGT[A/G]CCCTGAGCGCAAATA | 5607 |
rs188192575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702358 | GATAGTAATGATGGT[A/G]ACAATAATGTTATTC | 5607 |
rs188227562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717094 | AGTAGATCAAGTAGT[C/T]TGAAAAAAGAAGAGA | 5607 |
rs188228496 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581751 | ATTAACCAGTAGGCT[C/T]CTATTTGCACTGATA | 5607 |
rs188234811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625542 | CTCCATTCAAACTTC[A/G]TTAATCACTTTACAA | 5607 |
rs188242878 | snp | A/G | 0.000132743 | 0.00814578 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563366 | GTAAGTATACGACAA[A/G]TGAAGACTATTTTTT | 5607 |
rs188255782 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759208 | AATAGCCGGTGCTGG[C/G/T]GGGTGGGGGATGCTG | 5607 |
rs188362278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589771 | TTCCCAGAAAAAAAT[A/G]TGTGTGTGTGTATGT | 5607 |
rs188383743 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704486 | TTTTTTTAGTCAAAT[A/G]CTTTTTCTGTGAGTT | 5607 |
rs188385240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586749 | AACAAGCTAATTAAC[A/C]TTCATAGTGAAATGA | 5607 |
rs188394385 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659918 | AGTTCTACTGGAGTA[A/G]GAAGACTGTTGAAGT | 5607 |
rs188395648 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547148 | GATTTTTTCCTTTCT[C/T]CTGAGTTACCAAATA | 5607 |
rs188400224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739235 | TAATGAGCCATGATC[A/G]TGCCACTGCATTCCA | 5607 |
rs188404986 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701076 | GTTCCACTTTTGTGT[A/G]TGTGCGTGTTTTTTC | 5607 |
rs188410544 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778411 | TCACACCAAATGGCT[C/T]TGTTTCATTGTTAGA | 5607 |
rs188421748 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560673 | CAAATGCTCTTGTAA[A/T]GTTTCATAGCTACTT | 5607 |
rs188432101 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603597 | CCAAATTGCATAACC[A/G/T]CTTGTCATTGATCAT | 5607 |
rs188437858 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566041 | CCTACAAATTTGCAT[G/T]GGTCTTTATTTTGTA | 5607 |
rs188451018 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663722 | TACAAAAAATATTTT[A/G]AAATTAGCAGGGTAT | 5607 |
rs188452955 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636790 | TGCAAAGTATTGTTT[C/T]GGGGTGTGTCTGTGA | 5607 |
rs188457226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767701 | TTTTGCTCTTCAAAC[C/T]GATGGGACTTCTGTG | 5607 |
rs188460918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597052 | TGGGCGCCTGTAGTC[C/T]CAGCTACTCAGGAGG | 5607 |
rs188470327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784444 | TGTGAAGCCAATGCC[C/T]CTGTAGGATGCTTTG | 5607 |
rs188478234 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804622 | CCCTCCTGCAGTTCC[A/G]CTCTGCTTGTTCCAG | 5607 |
rs188508682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604194 | ACGAGCTGTGCTCTA[C/T]ATTATGAGAGTGACT | 5607 |
rs188518962 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622203 | AAGGGAGAATGTGCT[C/G]TTTTATGTAGGAAAG | 5607 |
rs188526156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736103 | ACTTTTAAAGTCACC[A/G]TGGGAAGGAAGTAAG | 5607 |
rs188549132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775314 | TCTTATGATGGTTTT[C/T]GGTCTTTATATCCTA | 5607 |
rs188556182 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780271 | GCCAGGGAGCAGATA[A/C]TTTTTTTTTTTTTTA | 5607 |
rs188579286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589453 | TCAAGTCCCATTGCC[A/C]AGGCAAGGCCTTTCC | 5607 |
rs188582509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687379 | TCTTTATTAAAAGAA[A/G]CATCCCTATTGTTCA | 5607 |
rs188586117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667896 | CCTGGAGTCTCTCCC[A/G]TAGTTTATATCCAGT | 5607 |
rs188590136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546437 | ATAACTGAGTGTCTC[A/G]GACCTGAAGTCAGCA | 5607 |
rs188592662 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706876 | CATACATGAGAAATT[G/T]TGGGGATTCAGTAGT | 5607 |
rs188615205 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722242 | GCGTTATACATTAAA[A/G]ATTGAAGCTTTCCTC | 5607 |
rs188621689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742811 | GAAGATTTACTTTGG[C/T]TCTTATACACCTATG | 5607 |
rs188621724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765068 | ATATCTCGTAAGTAT[A/G]GTACAGTATTGGCTG | 5607 |
rs188624750 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624277 | CCGGGAAGCGGAGCT[G/T]GCAGTGAGCCGAGAT | 5607 |
rs188626478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573695 | GGAACAGGTTAATAG[C/T]ATTTACCAAACAGAT | 5607 |
rs188657677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550299 | TGAGCATATTTCTAC[A/G]ATATAGCTTTAATTA | 5607 |
rs188664422 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720374 | CACACTTACACACAC[A/C]CAAGGAAAAAAAGAA | 5607 |
rs188670019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648316 | CATTCCATATAAATG[C/G]AATCTGATAATATAT | 5607 |
rs188679358 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725759 | ACCTGTTAAGACACT[A/G]CAGACTGTTGCAAAT | 5607 |
rs188690319 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762578 | GACAAAAAAAAAAAA[A/C]AAAACAAGCAGACTA | 5607 |
rs188699548 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766814 | CAGCTTGCATACTTC[C/T]GTGGAGTTGGAGGCT | 5607 |
rs188712132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803461 | TCACAGGGTTAAGGG[C/T]GTCAGTTACAGTCTA | 5607 |
rs188714403 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585342 | ACTAAATCTTAGCAT[A/C]TGTCAAGATTTGCAA | 5607 |
rs188729483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780509 | CAGATAAAGTAGACA[C/T]TAAACAGATAGACAA | 5607 |
rs188734593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659573 | CATGTGCAGGTAGAT[G/T]AGTATGAAATTTGAG | 5607 |
rs188748005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654874 | AAGATTAGCCTGGCC[A/G]AGTTGGTGAAACCTC | 5607 |
rs188754536 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621253 | ACAAATACCATGTAT[A/T]AATATGAAAACTCCT | 5607 |
rs188754561 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684980 | CAAGAAGTCTAAGAT[A/T]TATGTGTTAAGTGGA | 5607 |
rs188794329 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787247 | TGTTTCTCAAATTTT[G/T]CGAAGGTCTCTAGCC | 5607 |
rs188820225 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591589 | TTAGCCAGGATGGTC[A/T]CAATCTCCTGACCTC | 5607 |
rs188857641 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612999 | TTTAGCTGATAGTTA[A/G]AAGAGGAGTTATTTA | 5607 |
rs188880178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784333 | GGTTTAGAGAATTTC[C/T]GCTAAGTCAAACTAT | 5607 |
rs188880473 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569650 | GGTAGCAAGGAGCAG[A/T]AGCATATTCAAGTTT | 5607 |
rs188887518 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641099 | TTTATACCATTAATG[C/T]ATTCTATAAAATCTT | 5607 |
rs188914839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714092 | AGTGCTGGGATACAT[A/T]GGCAAACAAAATAGG | 5607 |
rs188937369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544776 | TCATTGTCTTGGGTA[A/G]CTTAATCAAAATTTG | 5607 |
rs188938515 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626358 | TGAAACCTTGTCTCT[A/G]TGAAAAATACAAAAA | 5607 |
rs188940246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661249 | ATCCATTTGAATCTG[G/T]TCTTCTATAAAGAGG | 5607 |
rs188942191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710590 | CTCATTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 5607 |
rs188942365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692340 | AAAAAATGCTTTTCA[C/T]TAAATTTGTGATTTG | 5607 |
rs188948455 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644025 | TTTTTATCTAGAAAT[A/G]TCTAGAGCCAGAAAC | 5607 |
rs188959007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726736 | AATCTTTGAAGTGGG[A/T]TGATGCTCTCTTAGA | 5607 |
rs188961834 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745686 | CAATATATCTGAGAC[A/T]GAAAAAGGAGATAAT | 5607 |
rs188968716 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660184 | CTGGAGTAGAAGAAA[A/T]GTTTTTTAATAATTT | 5607 |
rs188969727 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767364 | GCCAGTCCAGAATTT[C/T]AACCATCTTGGTAAA | 5607 |
rs188974463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754930 | TTGAGGTGGGTAGTA[A/G]GAGAAATGAGACTGA | 5607 |
rs188984016 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782850 | ACAAGCTTTCCTCCC[A/G]TCAGGGAGGTCAGCA | 5607 |
rs188984359 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635188 | GCTTTAGATATTTAT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs188995510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788610 | TATAGTAGTTGGAAA[A/G]TAATAGGTTCATAAG | 5607 |
rs188997331 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708039 | ATCAAATACAGGCTA[A/G]GCCTGGCGGCTCATT | 5607 |
rs189005507 | snp | A/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680840 | ACATGTTGTGATTGG[A/T]TAATGTTAACTCGTC | 5607 |
rs189035964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789781 | ATGAGGATTAACACT[G/T]CTTTCATATGTTTGT | 5607 |
rs189039716 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744233 | AAAAGAGAGTCCTTG[A/C]AAAATAGCCACAGCT | 5607 |
rs189045436 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710200 | TAGCATACGCATTTT[A/G]CTCTTTTCACTTGGA | 5607 |
rs189085604 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698377 | ATTTTTAGTAGAGAT[A/G/T]GGGGGTTGCGCCATG | 5607 |
rs189086837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666317 | TTGATTTTTCTTCTT[C/T]AAAATTAGAAATCAT | 5607 |
rs189091187 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629288 | GACAAATACTCATGT[C/G]AATGGGCAAAAACTT | 5607 |
rs189095504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648141 | TTTGATATACTCACA[A/G]GGTTGTGTAGTCATC | 5607 |
rs189103153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734418 | CATTCATTTATTTTG[C/T]AGTAATAAATTGTGC | 5607 |
rs189105157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715675 | TCTTGATATGAAGAA[C/T]AAAGAAAGACAAAGC | 5607 |
rs189119851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755645 | TGTCCCTATTCATAA[A/T]GATTCTTTTTAGTAC | 5607 |
rs189124515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558318 | ATCCCATTCATCAGC[A/G]AGTCCTGTTGGCTCT | 5607 |
rs189125354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771943 | CAGCCATCAAGTAGG[C/T]AGCTGCCCACAGTCA | 5607 |
rs189150282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594998 | TGATAGGGAAGATAA[A/G]AGTCACATTTAATGA | 5607 |
rs189156615 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611923 | TGTAGATGACCAATA[C/T]GAACAAACAGCTGTC | 5607 |
rs189179808 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634454 | TATAATGTCAATTAG[A/C]TCAAGTTGGCTGATA | 5607 |
rs189198812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665814 | TGTTAGTGTTACTTT[A/C]TCTGAGTATAAATAA | 5607 |
rs189199513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673276 | GCACAAGACAGTCCC[A/G]TCTAAGGGCATCCTT | 5607 |
rs189221509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571616 | TTTTTTTTTTCAAGT[A/G]CTTTTTAAGAAGGTT | 5607 |
rs189250505 | snp | C/T | 0.00756386 | 0.061089 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565189 | ACACTGTCTCTCCCC[C/T]ACCTTCCTCTTTGCA | 5607 |
rs189251078 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719008 | GAATTTTATTCATTC[C/T]AACTTTATTTTTGTA | 5607 |
rs189254014 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712271 | TAGGAAGACTTAAAG[A/T]TCCAGACGTTTGGAG | 5607 |
rs189255902 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737239 | GGCTATGGATCCCTG[C/G/T]GGGGAGAATGGTCCT | 5607 |
rs189258125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760502 | TTCAGCCAATAGACC[G/T]TATCCATTTCTTCTT | 5607 |
rs189267135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771573 | TTTTCCCAAGAGATA[C/T]AGCTACTTTGGAATG | 5607 |
rs189271458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776414 | CAGAATGTCCAGCAG[A/G]CCTTCAGAAAAATGC | 5607 |
rs189271784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607559 | CAGGATGTCACAGGT[C/T]GCTGAGCAGAGATTT | 5607 |
rs189272617 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553943 | AAAAAAAAAAAAAAA[A/G]AAATAGTTGAGAAGA | 5607 |
rs189274656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562931 | ATGGTGCTGTTTGGG[A/G]GATTTAAAAAGTGTG | 5607 |
rs189294992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599076 | GCTAGTTTAGCATCT[C/T]GTCACTTTATGTGCT | 5607 |
rs189303487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572762 | TGGAGTGCAGTGGTT[C/T]GATCTTGGCTCACTG | 5607 |
rs189303647 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552593 | GCACCCACCTCCACA[C/G]CTAGCTAATTAAAAA | 5607 |
rs189318886 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581004 | TGGCAGATAAAATAT[C/G]TAATTTACTAGAGTA | 5607 |
rs189334147 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711640 | AAAAATAGCCATAAC[A/G]TGATTTACACACGCA | 5607 |
rs189347681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747760 | CATAATTAAAGTTTT[C/G]CTCACAAAATAGGGG | 5607 |
rs189374399 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794613 | CATTCCACTGAGGGT[C/T]GGGTAACTCTGGAAC | 5607 |
rs189453659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622603 | TTTGTCAAACATTTA[C/T]GAAGTGAGGAGCACC | 5607 |
rs189469805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604566 | ATATAATGTCTTATG[C/T]CTCAGTTTTCCCATC | 5607 |
rs189470661 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779908 | AAGTATGTTACACTT[C/T]AGTTCCTCATTGGCC | 5607 |
rs189487681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732196 | TGGAGCTGCCTATAG[C/T]TAATCATGTAGATCC | 5607 |
rs189493043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652961 | TGTAGCATGTGTCAG[A/T]ATTTTCTTCCTTTTA | 5607 |
rs189495423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693185 | CATCTTGAGCCATCT[A/G]ACTAAAAATTGAGTG | 5607 |
rs189503980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771128 | TTCTTAAAACACATG[A/G]TAATGTGTACCATGT | 5607 |
rs189531471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595648 | ATCAAGCACTTTAAA[A/G]AAAGTTTAACACTTA | 5607 |
rs189539481 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558865 | CAGGATTTTGTTTGT[G/T]TTTTCTTTTTTCACT | 5607 |
rs189549495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590299 | GTCTGAGATTCTCTC[A/C]AATGTAACCTATTAA | 5607 |
rs189554742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654958 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCTGG | 5607 |
rs189565205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697425 | AAGTTCACAAAGCTC[A/G]TAAGTGTCAATCAGA | 5607 |
rs189571328 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629774 | GATTTTTAGTTCTTC[A/G]AAACTTACTTACTTC | 5607 |
rs189581164 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575941 | TTTTTTTTTTTTAAG[A/G]TGGAGTCTTGCTGTG | 5607 |
rs189613385 | snp | A/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547177 | TACTATTGGCTGTTT[A/T]TGTCTTTTGTTTGGT | 5607 |
rs189613660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727853 | ATTTAGTACTTGTCT[C/G]TCTTAAGGAGATCTG | 5607 |
rs189636314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557371 | CATGTGGTTTCACTT[C/T]TCTATTACACTCATG | 5607 |
rs189647468 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799863 | TATCTCTTTTATAGG[A/C]GAGGCCCTAGTGGGA | 5607 |
rs189655125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680546 | GTTTAAGTTTTAAAG[A/G]CACTTTGAGGCTGAT | 5607 |
rs189676137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699356 | CAGAGGAGATTTTCT[A/G]TTCCCTGCTAGAAGC | 5607 |
rs189683472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716290 | AGGCTGCAGTAAGCT[A/G]TGATCATGCCATTGC | 5607 |
rs189685667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735301 | AAATGTGAAATTCTT[C/T]ATTAAAGATAAATTA | 5607 |
rs189690632 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758346 | GGCTTGGGCAGTCAG[G/T]TGCATGGTGGTACTC | 5607 |
rs189712022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581271 | TGGTATCTGGTTTTT[C/T]GAGGAGGTATTTTCT | 5607 |
rs189727913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639983 | TTTTCTTCTTTGAAC[C/G]TCTCTAGAATTCCCT | 5607 |
rs189732417 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652291 | ATTAGCCATGATATT[A/C]GTCCATCTTGTGTTG | 5607 |
rs189732655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617663 | TGTGTGGACTTTTTA[A/T]CATGTTATTTTCACA | 5607 |
rs189737162 | snp | A/G | 1.65277e-05 | 0.00287464 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658639 | TGGCTTCAGTGTTAG[A/G]AAATTTGAGTGATTT | 5607 |
rs189757173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714779 | GCACTAACTTGAACC[C/T]CAAAGGTCACACTAA | 5607 |
rs189765230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754422 | CAGCTAGAAAAATTT[A/G]TATTTTTATTTACTT | 5607 |
rs189804125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637419 | GAACTAATTTTCCCC[A/G]TGCAGCAGAGGTAGT | 5607 |
rs189815840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577510 | TTGTTACATTTCTGT[C/G]CAAGCTATTATGTTC | 5607 |
rs189822984 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795609 | ATCAGATCTTTGTTA[A/C]TTGTTTAGACTCCCT | 5607 |
rs189831770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613872 | TCACTTTTCAGAGGT[A/G]CATTTACTCTTTGAC | 5607 |
rs189836694 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737844 | GGGGAATAGAATAGT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs189848867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806029 | CAGGGCAACAGGGCC[A/G]GCCCCTCCAGAGTCC | 5607 |
rs189854700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564756 | TCCTGAGAATGTGAC[A/T]TGCTTATTTTTAGAA | 5607 |
rs189873547 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683086 | GCGGAGGTTGCAGTG[A/C]GCTGAGATTGGGCCA | 5607 |
rs189877149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602594 | CCAGCAGAATTTTTA[C/T]GAGACATAATATTCT | 5607 |
rs189882240 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719252 | GATACGTAAGAGGGC[C/T]TTGTCGGTTAAGACC | 5607 |
rs189882911 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620830 | GGTAACTAAAACAGT[A/G]AATAGAATGTGTAAC | 5607 |
rs189891336 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644924 | GAGGCTGAGGTGAGC[A/G]GATCATTGAGGTCAG | 5607 |
rs189895448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584739 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 5607 |
rs189957641 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600545 | AAATTGGACAGCAAA[C/T]GTTGTATTGATCTTC | 5607 |
rs189967314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563063 | TGAATGACATGAGCA[A/G]TATTTTAATTTTCTG | 5607 |
rs189971340 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632488 | GACTGAAACTCAGAA[A/C]GCTGAATTGTCAAAG | 5607 |
rs189996739 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683716 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTTTAG | 5607 |
rs190008811 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662647 | TAAGTTTTTAATGGT[G/T]ACCACTGATTAAATT | 5607 |
rs190010905 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703165 | AATTTCTATAGATCA[C/T]CTATATACTGTATGC | 5607 |
rs190017071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635934 | CATCTTTAATGTCTC[C/T]ACTTAACATGTTTAA | 5607 |
rs190025810 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678297 | GCTAATGTGCCCTCT[A/G]GCTCCTGGTAAACTG | 5607 |
rs190026957 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738333 | GTAAAATCCTTTAAT[A/C]AAAAGAAAGTTCCTG | 5607 |
rs190030467 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638942 | TCTTACAAATTTGTA[A/T]AGACCCCTTCCTTAT | 5607 |
rs190030625 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719979 | TAGTTATATACCCAG[A/G]TATTTTCATTAGTAT | 5607 |
rs190036557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706207 | TGGGTGCTAGGGGTA[C/T]AAAGATTAATAAAAA | 5607 |
rs190044228 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761711 | TGTGGATGTGGTTCA[C/G]ATGTTTCAATCTTAA | 5607 |
rs190052144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669730 | TCAAGGTTGCTTAAA[C/T]TGTTAACAGTTTAGT | 5607 |
rs190055654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737689 | GAGGCAGTTGTCTGT[C/T]TATGCACAGAGCCAA | 5607 |
rs190061409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803894 | CAGTGGGTTTGGGTT[A/G]CAGACTTGTGGTTCA | 5607 |
rs190065739 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777167 | TTGCTTGAGGGTGGG[A/C/G]TGGGGTGCTTTCTAT | 5607 |
rs190109581 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802368 | CAGCCCTGTTGGTGA[A/C/G]GGTGTCTGCCCAGGT | 5607 |
rs190140138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702931 | AAATGCAAATAAGTG[A/G]TAATATCATATAATG | 5607 |
rs190148366 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742084 | TATCTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 5607 |
rs190157053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708863 | AAACTTTAATATCAG[A/G]CTATCTTTTATCCAG | 5607 |
rs190159911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623289 | GTGTGAATAAACTTA[C/T]AGTAGTGGGCAAGAG | 5607 |
rs190161011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689780 | GTCAGATGTATCTGA[C/T]TGAAACTAAAGATTT | 5607 |
rs190164902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779745 | TGTCATCTTCCTAGT[A/G]TCTTGTTTCAAGGCA | 5607 |
rs190167111 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724595 | TCTTCATGCAGCCAT[A/G]TCTACTAAGAAACCA | 5607 |
rs190169580 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639697 | ATTCAAGATCCTCCA[A/C]GACATGTCGTCAGTC | 5607 |
rs190179623 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745536 | GAAAAAGGTAAACAA[C/T]AAAGAGTTTAGCAGT | 5607 |
rs190188007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766302 | ACCTCCGTGCTTAGA[A/G]GTTCAACGGAAAAGC | 5607 |
rs190198321 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781560 | TAAACGTTAGGCCTT[A/G]GTCTACCGAGAGACA | 5607 |
rs190205206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549306 | TTGATGTCAGATTAT[A/G]TACCCTTTTTAGATT | 5607 |
rs190225337 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605190 | CCCTAGAGTAGCTGG[G/T]ATTACAGGCATGTAC | 5607 |
rs190237464 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568171 | GAGAGTATGGCATAC[A/G]TTTTACTGTAGTGCC | 5607 |
rs190243388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588406 | CTACCCATCCCCAGT[A/G]CACACCAGGGACCTC | 5607 |
rs190255595 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658891 | TTCCAACTTCTTCTG[A/G]AAAAAAAATGCTGTT | 5607 |
rs190266207 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686941 | GTGGAATGCAAAGAT[C/T]GGTTTGAGGATGACT | 5607 |
rs190271441 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579107 | GCAGTAATTTTTTTG[A/C]CAGCCACTGATTGGA | 5607 |
rs190286705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656993 | TTTTTCACCTATGAC[A/G]TTTATCTCTAACGGA | 5607 |
rs190287319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702670 | TAGCCTCTTTTAGAC[C/T]GGGTATTTGCTATAC | 5607 |
rs190314692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694574 | ATACCATCTCACACC[A/G]GTTAGAATGGCGATC | 5607 |
rs190319520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685244 | AGAAACAAAGATAAG[A/G]TTGACAGCCGACTTC | 5607 |
rs190323428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712594 | AAAAGGAACTTTCAG[A/G]GAACAGCAAGAAATA | 5607 |
rs190324854 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728189 | TTGTGTGACATTCGG[C/G]ATTGTTTTTTTTCCT | 5607 |
rs190325465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728759 | TATTAACTTGCTATT[A/G]TTATGCAAATAAGTG | 5607 |
rs190344241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769309 | AATAATCATTAATTT[C/T]TCATTTACACTTTCC | 5607 |
rs190344651 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553351 | ACTACTCCAGGTTTA[C/T]GTTCTGTGATATCAT | 5607 |
rs190347788 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625772 | AGCATCTTTATTCCT[C/T]GAAATCGAACCCAAA | 5607 |
rs190351686 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785247 | ACCGTGCCCGGCCCC[A/G]AACTGTTTCTTAAAC | 5607 |
rs190359348 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590704 | AGCGATCCTCCTTCC[C/T]TGGCATCCCAAAGTG | 5607 |
rs190381868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660588 | TTGCCAAGTCAAAAG[C/T]AACAGAATCAGAAAC | 5607 |
rs190385532 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542194 | TTGGAAGGGGGGATA[A/C]AAAAGAACTATTTCT | 5607 |
rs190401830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764622 | CACAATGCCAGGCTC[A/C]TTGCGTTCCACATGG | 5607 |
rs190417578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662675 | ATTTTCCACATAGAA[A/G]GTAGTACTTGTCACC | 5607 |
rs190436103 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736792 | TCATGTGGCAGCTTT[G/T]CTATTATCTCTCCCT | 5607 |
rs190465198 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805094 | CCCAGCTGGGCTCCA[A/G]GCCTAGCTCCACCCC | 5607 |
rs190490263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610999 | CACAAAATTAGAACT[C/T]GCTTTAGGGCACAAT | 5607 |
rs190494217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587153 | AAGGGCGTTTCAGAC[A/G]GAGGGAAGAGGGTAG | 5607 |
rs190500190 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548078 | TGCCTTGTTTATGTC[A/G]ATGGGCTAAGGCATG | 5607 |
rs190512331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579945 | AGCAGTTTTCATTGT[G/T]GATATTTTTCCACTA | 5607 |
rs190512671 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647654 | ACTTTGGGAGGCCGA[A/G]GCAAGCGGAGTTTGA | 5607 |
rs190521217 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669802 | GATAACAACAAAAAA[A/C]CTGATAATATGAAGT | 5607 |
rs190535139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630279 | AAAAGGTCTTGATGG[A/T]TAGTAATGGTATTTC | 5607 |
rs190539113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596291 | GCTGGGTGTGGCGGC[A/C]CATGCCCAGCTACTT | 5607 |
rs190546781 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682445 | GGCCAGGCTCATTTC[A/G]ATCTCCTGATCTCAT | 5607 |
rs190547208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615189 | TTTTAGTAGAAACAG[C/G]GTTTCACCATGTTGG | 5607 |
rs190586303 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608418 | AGGGCGTGTCAGATG[C/T]TGGGGACAGCCTAGC | 5607 |
rs190589661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723058 | ATTCTGAGTAGGAGA[C/T]TTGATTACTAAAAAC | 5607 |
rs190617045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643039 | GGAGCTTTACAAAAT[A/G]ACAAAGATGTGGGCC | 5607 |
rs190637481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589022 | TTTTTTTAATTTTTA[A/G]TTTGTAGAGACGGGG | 5607 |
rs190647409 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649199 | CTTCTTTTGAGAAAT[A/G]TGTTTTCAAATCCTT | 5607 |
rs190653877 | snp | G/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614512 | TATATTGCCTAACAA[G/T]TCCAGTTCTTTCATT | 5607 |
rs190655261 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649884 | ATTTCTCCAAAAAAA[G/T]CCAGCTGGGATTTTG | 5607 |
rs190665088 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624360 | AAAAAAAAAAAAAAA[A/G]AAGTGGCACAGCTGG | 5607 |
rs190665488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688570 | TAATTGCCACAGTAG[C/T]AATAGAAATTATTTT | 5607 |
rs190669462 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669191 | ACATCAATATGTGAA[A/G]CAAAAGATTTCTATG | 5607 |
rs190678825 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699970 | GGGATCTTGCCAATG[A/T]AAAAAAAAAAAAAAA | 5607 |
rs190681709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687942 | TGATGGAGGTAAATG[A/T]TAAGAAGAACACTGA | 5607 |
rs190684148 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707859 | CAAATGTCAAAGTAT[A/G]CAAGGTCTCCCCTGG | 5607 |
rs190689108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748809 | AAAAACAGACTATCC[C/T]GCAGGCTGGTCCTCA | 5607 |
rs190691573 | snp | A/G | 3.31708e-05 | 0.00407238 | missense | MAP2K5 | GRCh38.p7 | 15:67772712 | TCCACTATAGTATGC[A/G]AAAACAGCCAAAAGA | 5607 |
rs190702406 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785032 | GCAGCCTCAATCTCC[C/T]AGGCTCAGGTGATCC | 5607 |
rs190738452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567122 | TTGTCTTTTAAGAAA[A/G]TGTAAAGTAATTTGG | 5607 |
rs190743486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792343 | AAACCTTTTATTTTT[A/G]GATGTGAGGTCTTTG | 5607 |
rs190752490 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735535 | GATGTGGTCTCTGCT[C/T]TCAAAAGAGTGCAGT | 5607 |
rs190754582 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758999 | GTCTATATGAATGAC[C/T]GCACATCTTTCAGTT | 5607 |
rs190754955 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599995 | GAAAAACATGCAAAC[A/T]TATATATAAAGTTAC | 5607 |
rs190764400 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775105 | GCAGAGTGGGCACTT[A/T]GGTGGTGAGGTCACT | 5607 |
rs190774768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792827 | GGCCCAAAGCGGCCC[C/T]GTATGTCTTTAATGA | 5607 |
rs190775747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629073 | TTTGCCAAACCATGA[A/G]ACCAAGGTGGCCATG | 5607 |
rs190799616 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653307 | TTTTTTTTTTTGAGA[C/T]GGAGTTCTGCTCTTG | 5607 |
rs190804109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574195 | GAAGCCACTTAGGGG[A/G]CTGTTCCTTGTGAAA | 5607 |
rs190809177 | snp | A/G | 0.000544874 | 0.0164967 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693571 | TGCTTATATGGCGGT[A/G]AGTAAACTTATGCAA | 5607 |
rs190813175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674094 | CCTTGTGATCCACCC[A/G]TCTCGGCCTCCCAAA | 5607 |
rs190820314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609392 | AGAATCTATAGGTCT[A/G]TAGATTCTATAGACC | 5607 |
rs190849029 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743541 | GCCAGAGTAAATTTT[A/G]TTCTCTTCCTTTATT | 5607 |
rs190867686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619569 | TCCCCTTGAAACTTA[C/T]AATAAAGTAGAACAT | 5607 |
rs190874341 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617938 | GACTCAAGCAATCCT[C/T]CCACCTCAGCCTCCC | 5607 |
rs190876278 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635086 | CAGTGGTGTATTTTC[A/G]TTTCCCTCATCCCAG | 5607 |
rs190877483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592531 | GACTTAAATTATCTA[C/T]TTTGTCTTTTGAAGT | 5607 |
rs190881490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601761 | AAAATCCCAGAACAT[C/T]CCCTACTCATTGATG | 5607 |
rs190885153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777695 | AGAGAAACAAGCTGG[C/T]GAAGAAATTTTCTTT | 5607 |
rs190885276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752135 | GAGTGGCACAACCTC[C/T]GCTCACGGCAACCTC | 5607 |
rs190886200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574695 | AACATGGGGAAACCC[C/T]GTCTCTACTAAAAAT | 5607 |
rs190888849 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555753 | AAATGAGCTTGAATA[C/T]CTTCTCATTTGTATT | 5607 |
rs190889666 | snp | A/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629869 | AAATTTTTATTGTAT[A/T]AAAATGTGTTGCAGA | 5607 |
rs190896549 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605688 | TTGCTTGGTGTTCTT[A/C]CCCCAGGCAGTGTTG | 5607 |
rs190898203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569199 | AAGAGGTTAGAAGCT[C/G]ATTTTCCACATGGTG | 5607 |
rs190908937 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629698 | TCCTATCCTAACACT[G/T]ACCAGATGAGAGGAA | 5607 |
rs190917182 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668597 | ATATTAATAAACCTA[C/G]AGCTCCAGTCATAGC | 5607 |
rs190964029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675678 | ATCTATAGTTATCTC[A/C]AAATTAAAAGCTTAA | 5607 |
rs190978719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713222 | AATAGAAATTTTCCC[A/G]AGGAAAATTTACTAT | 5607 |
rs190984673 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774535 | AAAGATTGGGCCCAA[A/T]AGGGGATGGGAAAGA | 5607 |
rs191010401 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595976 | CTAAAGTTATTTTTT[C/T]TTTTTTTTTTTTTGT | 5607 |
rs191016049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578293 | AGAGGTACCATGCAT[A/G]GCCCTGCATTTTATC | 5607 |
rs191020116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596086 | AGAACTAATTCTGGT[C/T]CAGCTGCATCTTTTG | 5607 |
rs191031277 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591901 | CAGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA | 5607 |
rs191035854 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559733 | AAATCATATTACTAT[G/T]CTCCAGGCAACTAGA | 5607 |
rs191074460 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627427 | CTGTATAATTAATTG[A/T]TATAATAAAAGTTAA | 5607 |
rs191097635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657797 | TTGTATATGAATACA[C/T]GATTTTTTTACAGAT | 5607 |
rs191098072 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738486 | ACAAGTGACAAATTA[A/G]GTCACTGACAGTATA | 5607 |
rs191104443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762229 | TAAATGAAATCCCTT[C/T]GGTATGAGACAAGTA | 5607 |
rs191107974 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698811 | GGCTATGCTCATGCG[A/T]TGGTAGTAATGGTAG | 5607 |
rs191109395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554343 | GGATTACAGGTGTGA[A/G]CCACCGCACCTGGCC | 5607 |
rs191114577 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778008 | TAAAATCAGAATAGC[A/G]CTCTTGGATTTTTTT | 5607 |
rs191118838 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630660 | TATAAAAGGAGGATA[A/T]TAATGTATCAGTATT | 5607 |
rs191125208 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681878 | TGCCTTCAATAAAAC[C/T]AATTGATAAACCCTA | 5607 |
rs191125689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796638 | ATTTGAGTGAGGTCA[A/G]ATATCCAAACTATTT | 5607 |
rs191128397 | snp | A/G | 0.000653982 | 0.0180711 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642485 | GAGATGAATTTTGAT[A/G]GAGGACTTTGAGGTG | 5607 |
rs191132902 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729645 | GCCGGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 5607 |
rs191135680 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660541 | TTTCCCTTGAGTTCC[C/T]TCATGGAGGCCAAGA | 5607 |
rs191140727 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795758 | TTTCTCAAATATTTC[A/G]TGGCTGTACTAATTT | 5607 |
rs191148315 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769997 | GAACGGACGTACGAA[A/G]CTTATTTTTATTAAT | 5607 |
rs191175408 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693920 | TCAGTCAATAAAATT[G/T]TTTTTTTTTTTTCTT | 5607 |
rs191198971 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654470 | GTTGGATCATTTTTT[A/T]AAAAATCAATTCTGC | 5607 |
rs191201523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695680 | GCTTTAAATTCCTCT[C/G]ATAATTAAATTGCAT | 5607 |
rs191212112 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599685 | ATTCCCTGGAAATTG[A/T]TTTTTTTTTTTTTCA | 5607 |
rs191234968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735017 | AAAATATCCTGATAT[C/T]TCAAGCATAAAATCA | 5607 |
rs191241614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702435 | TGAATTGGATATTGG[G/T]GTGTAAGTTATGATC | 5607 |
rs191253484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736757 | TTGAAAGTTAATGAA[C/G]TTGGTGTTCAGTCTG | 5607 |
rs191254038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773467 | TTCCCTGCCTTTAGA[C/T]TACTACAGTCAGAGC | 5607 |
rs191265830 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802647 | GGTTCCACAGACATG[C/G]CTGTGCAGAAATGGT | 5607 |
rs191265958 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760152 | TTCCTTTAGTAATTA[C/T]TTTTTCTATTGGTAA | 5607 |
rs191274733 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776078 | TGGGAAAGGTGTGAC[C/T]TTCAATTCTTTAAGA | 5607 |
rs191278492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562782 | GTTATGAGGTTTTCA[A/G]GGAGGTATTGCATAT | 5607 |
rs191306443 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598553 | GCCTGTGCCCTGACA[C/G]TGTTGGATGCTTACT | 5607 |
rs191310896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615882 | ATACAGCAGAGAAGC[A/G]TTCTGCATGTTTTGT | 5607 |
rs191319104 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580660 | TATGTATATACCAGC[A/C]ATTTACAAAAGTACT | 5607 |
rs191330181 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615299 | CACTGTGCCCGGCCT[A/G]TTTCTTAACCACAAA | 5607 |
rs191350914 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650576 | GCCTGTTTTATATCT[A/G/T]TTGAAATAATCGTGC | 5607 |
rs191360355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680076 | GCAGAAACATACCAC[A/G]TGAAATCTTTGTGCC | 5607 |
rs191362645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715905 | AATCATTTGCCTTTA[A/G]AGGTAAAAATGTCCC | 5607 |
rs191380908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704938 | CCTGGATTACAGTTC[C/T]AGGTTTGCTACTAGT | 5607 |
rs191387199 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655124 | CTCAATTTCTTCTCA[A/T]CTTTTTTATGCTATT | 5607 |
rs191403816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720768 | TTTGCTTCAGTGGCT[C/T]GAAAGCACATATGCT | 5607 |
rs191412092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720535 | ATCTTTACCCAGCCA[C/T]CAGAATGAAGAAAGA | 5607 |
rs191412343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741433 | GACCAAGAATGGTTA[C/T]TGGGGTTCCTGGAGC | 5607 |
rs191412607 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763412 | CAGGAGCACCTATTC[A/T]TCTCTTTCCCACCTT | 5607 |
rs191422722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779087 | GCTCATTAGCTATGC[C/T]GCCCAGAATTTGCAG | 5607 |
rs191437155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544007 | CCTCTGCCTCCTGGG[C/T]TCAAGCGATTCTCCT | 5607 |
rs191439677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620286 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 5607 |
rs191447823 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583984 | AAACTCCTGAGCTCA[A/G]GCAATCCTCCCACCA | 5607 |
rs191458001 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653866 | AGAAGTTTTGGTATG[C/T]TGTGTTTTTATTTTC | 5607 |
rs191468475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685938 | AATTTGAGTAGTTAC[A/G]ACAAAAAGCTTATAG | 5607 |
rs191474246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665651 | CTTTTTAATGAGGGT[A/G]TCTAGATTTTGACAA | 5607 |
rs191486281 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756056 | GCATCTCTCCCCCAC[A/C]CTAGGGCACAAAGGC | 5607 |
rs191501534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791328 | ATTTTCTCTAAGGCA[C/G]ACTCTGACTTTGTTA | 5607 |
rs191531239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763078 | TGATGTGGAGTAGGA[A/T]GAGTAAAAGGCGGGC | 5607 |
rs191548394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564177 | TTTCTTGGCCCTAGG[C/T]AAATCACTTAACCTT | 5607 |
rs191552321 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797767 | GGCTCACTGCAACCT[C/G]TGCCTCCTGGGTTCA | 5607 |
rs191569952 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563839 | GAAAATGAACTACAG[A/G/T]GCTACTTACTGAATC | 5607 |
rs191580815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570781 | AGTTGGTTAGTTTAT[C/T]GATTATTGCTGTAAT | 5607 |
rs191582142 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604770 | CATGGTGGTGGGCGC[C/T]TGTAGTCCCAGCTAC | 5607 |
rs191586816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589864 | TACCTTAGAGGTCTG[C/T]ATTTTAGTATCCTTT | 5607 |
rs191602238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551542 | CTTGCTATGTTGTCC[A/C]GGCTAGTCTTGAACT | 5607 |
rs191609056 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625441 | GAATCAGGTAATTAC[C/T]GTGGCAACAACAAAC | 5607 |
rs191618358 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641898 | CTCACAAGAATACAC[A/G]GGGGAAGGAGAATTA | 5607 |
rs191625503 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607179 | CCTTGCAGCCAAGAT[C/G]ATATTTTAAAGAAGC | 5607 |
rs191666637 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704675 | ATGCATCAGCTGAGA[A/G]GTTAGCGATAATGGT | 5607 |
rs191679071 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739414 | TTAATTCACAAGATT[A/G]TGTGTGACTATATAT | 5607 |
rs191705239 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602178 | TAAACGGTATCTTTT[A/C]ATCTTAGTCTTCTCT | 5607 |
rs191707135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780982 | GAGCCAAAACCTAGA[A/G]GAGACCTCCTGGCTA | 5607 |
rs191725719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635217 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCTAGGC | 5607 |
rs191727774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674828 | GAAGAGTATACACAG[A/G]TGGCAAATAAGCACA | 5607 |
rs191736690 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661044 | GGTCTAATAATCTGG[C/G]CATGCAAGGCAGGTT | 5607 |
rs191738595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660208 | ATAATTTTGCTCTTT[A/G]TCTGCCACGGAAATG | 5607 |
rs191754402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681398 | AGGTTTAAATGATTC[A/G]TCCAGTCTCACAGTC | 5607 |
rs191784342 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744118 | CCTTCCTTTCATAAA[G/T]ACTTTGGATCATAAT | 5607 |
rs191787848 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711295 | TTAATATAAATGCCC[C/G]TAAGTGTTTGGAGAA | 5607 |
rs191789409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727058 | ACAAAAATTAGCTGG[A/G]CATGATGGTGTGCGC | 5607 |
rs191793272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746797 | AGAGCAATGAGTGGG[C/T]GCCGTGTTCATTTGA | 5607 |
rs191801454 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778717 | GTTTACTAGAAGCAC[A/G]GGGCTCAGATCAATT | 5607 |
rs191807526 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767519 | GCTTCCTCACTGATC[A/G]GAGTCCATCATTTTT | 5607 |
rs191815559 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784347 | CCGCTAAGTCAAACT[A/G]TTTCTTGCAGTTAGA | 5607 |
rs191820922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803898 | GGGTTTGGGTTACAG[A/G]CTTGTGGTTCAGTCC | 5607 |
rs191840762 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600656 | CCACAGCATGACACC[C/T]TTTTTGTTTTTCTTT | 5607 |
rs191880715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622837 | GGCGTGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 5607 |
rs191880910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627946 | TGAGAGCCTGAGGAG[C/T]CATTTTAAGCAATGG | 5607 |
rs191887062 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587666 | AGCGCCCACTCATAA[C/T]GTTTTAGTTAAGCCC | 5607 |
rs191889337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560464 | TAGGTATCCTATTAA[A/C]CCACAACAACTATTC | 5607 |
rs191909492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662983 | TAAACTTACAGAAAA[G/T]TTGTGAGACTAATGC | 5607 |
rs191916034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703463 | ACTAATATATTCAAT[C/T]AGGAAAAGTGAAGAT | 5607 |
rs191930329 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563881 | AATATATTCTGAAAC[G/T]ACTTTTCTTTTGTGT | 5607 |
rs191930959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574751 | GGGCGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 5607 |
rs191937265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546477 | TCCAGTCACTGTGCA[A/T]CAAATAGCTGGGAGA | 5607 |
rs191963285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628690 | TGTGAATGGCCACAA[C/T]GGTGAAGTTAGGAAA | 5607 |
rs191974777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593454 | TTGCCTAGTAGACTG[C/G]CCATCTAAAGCTGAA | 5607 |
rs191978176 | snp | C/T | 0.00823712 | 0.0636452 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806806 | GGAGAACAACCCACC[C/T]GTCGCCCTTCTCCGT | 5607 |
rs191985304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566112 | TAAAGGCATAGGGAA[A/G]ATACTGACAGATTAC | 5607 |
rs191991386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766094 | ACTGAAACCTCTGAG[A/G]CTTGGAAACTGTCCT | 5607 |
rs192007672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801965 | ACTAAGGGCAGACAG[C/T]GAGGTGTCATTAAAT | 5607 |
rs192064685 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549670 | AGAGATTCAGACCTA[C/T]GTCAGTCTGACTCTC | 5607 |
rs192083022 | snp | A/C | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723358 | ACTGAAGAGCATTTT[A/C]TAGATTGTGGTTGGC | 5607 |
rs192116504 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731493 | CATAACTTCCTTGGC[A/G]TGCAGTTTAGGGTTC | 5607 |
rs192116528 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714541 | GATTGTGAACTGGTC[C/T]GAGGGGTGACGGATG | 5607 |
rs192137387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770679 | CTTGCTAACCAAAAT[C/T]GTTGTGTGCCATCCC | 5607 |
rs192140538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550559 | TTTAGTCCTTCCTTT[C/T]TCCCCACAGTTGGCC | 5607 |
rs192142623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570020 | AAGGTCAGTGTGGAC[A/G]CTACCCCAAGCTAAC | 5607 |
rs192144150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625559 | TAATCACTTTACAAT[G/T]AATGTGTTGAGGAAG | 5607 |
rs192147152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787373 | CTATCAGGGAAAATC[A/G]TTAGTATGCTAATCT | 5607 |
rs192157884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651340 | AAAGTAATGGAGATA[C/T]GTATGACCACAAACA | 5607 |
rs192163046 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690034 | GTGTGCCATTTTTTT[A/T]AAATCTCTTCAGCTA | 5607 |
rs192177954 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725193 | TCTCTCTGTTGTCTT[G/T]CATGGCATTGTCTTA | 5607 |
rs192201339 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645597 | TTCTCTCTTTCACCC[A/G]GGTGGGAGTGCAGAG | 5607 |
rs192214195 | snp | G/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703569 | TTCCTTGTGTGGCTT[G/T]TGAACTGACTCTGGA | 5607 |
rs192230039 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741716 | GATAGAGGGCAACCA[A/G]AATACCAACTGATCA | 5607 |
rs192236397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684021 | ACTGAGCTGAAAAGA[C/T]AGAATTTGGAGTTCA | 5607 |
rs192247199 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582688 | TTAGCCGGGCGTGGT[A/G]CACACTCCTGTTGTC | 5607 |
rs192262379 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541144 | AATATCTGAAGGATC[C/T]GACTAAATGAATTTC | 5607 |
rs192264933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691401 | GTTACTGTGTGTGAA[C/T]TTGAAATTTGAATTA | 5607 |
rs192272892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671529 | TTATCAAATCAAAAG[A/G]CATCTTTAAGGGAAA | 5607 |
rs192274839 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710324 | GCGTCATCTAGTCCT[C/T]GGAGACCCCTCTTCA | 5607 |
rs192279415 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766600 | ACAGTGAAACTGGAG[C/T]GCAAATTTACTGTAT | 5607 |
rs192286323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726126 | TGAAAATCCATACAC[A/G]TATCAGTGTATATTT | 5607 |
rs192304259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786926 | ATTCCAGGGAGAGAA[A/C]ATGGCACAGGCTGAG | 5607 |
rs192307768 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599586 | TTAAAGCTTTGCTAT[A/G]CTGGTCTGAGAGCAA | 5607 |
rs192317231 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793936 | TAGGCACATAGAAAC[C/T]GCTCCACACATCCAT | 5607 |
rs192338308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616480 | CATGTCTCTGATGGA[C/T]GTCCTATAAATCCCT | 5607 |
rs192341663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651615 | ACATGTGAGTGAGAA[C/G]ATATATGTCTTTCTG | 5607 |
rs192344854 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631900 | GCTAACAAACTGGTC[A/G]GGCTTGCCTTGCCCC | 5607 |
rs192347410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720251 | ACAAACATAAACACA[C/T]GCATATATATACACA | 5607 |
rs192349039 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771172 | TAATGTGTACCATGT[G/T]TTTTACACATGGTAA | 5607 |
rs192355000 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575357 | GAAGTAGGAAAACCC[A/T]TGGAGGTGGCGGGGC | 5607 |
rs192445478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677268 | TAGTCGAAGCCTCTA[A/G]TTTTGTGTCCTTGGG | 5607 |
rs192449116 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557971 | TTAACATGTAAGAGT[A/T]AATTATGCATCCTAG | 5607 |
rs192462586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636618 | GGAATAAGAGAATAG[C/T]TACTCTGCTTGAGCA | 5607 |
rs192464889 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754493 | TGCCAGGTGCCGAGA[G/T]AAATCCCTGTGCTGG | 5607 |
rs192468777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611153 | TAAACATAAAACTTA[C/T]TAAATCATAATTAAA | 5607 |
rs192472499 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610804 | AGCATTAAATTTTTT[A/T]AAAAAAACATTAATT | 5607 |
rs192473492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576159 | TGATCTCAGGTGATC[C/T]GCCTGCCTTGGCCTT | 5607 |
rs192474710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654826 | AGCACTTTGGGAGGC[C/T]GAGGTGCGCGGATCA | 5607 |
rs192475130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621228 | AAATACAAATATTTA[C/T]AACTGAACCACAAAT | 5607 |
rs192504038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647570 | TAAGCAATATAGTGA[A/G]ATCTCATCTTTACAA | 5607 |
rs192514815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764464 | AAACCTCAGTGCCCT[C/G]CTGTTCATCCTGAGT | 5607 |
rs192521598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779678 | CTTGCCTGTTTAAGA[C/T]TGTAGTTATTTGAAC | 5607 |
rs192529474 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670762 | TGATTTAAAGGATAT[C/G]TACAATGCCAGAAAG | 5607 |
rs192530740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799156 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 5607 |
rs192534024 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631363 | GCCATGGTCTTGGAT[C/T]GGGCTCACATTACCT | 5607 |
rs192539258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607594 | ACTCAGTTTCCACCC[A/G]AATTAACTATTATTG | 5607 |
rs192564239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676152 | GTTTGATTCACCAAG[C/T]CCCGCAGTTAGCTCT | 5607 |
rs192566483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709927 | GCTGTACAAATACAT[A/G]TTCTGGTTTGGGATT | 5607 |
rs192570290 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714094 | TGCTGGGATACATTG[A/G]CAAACAAAATAGGCA | 5607 |
rs192574066 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743046 | ACTAATTTATGGCTG[G/T]GATGATTTTCTGTCT | 5607 |
rs192574590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695894 | GAGTGAATTCTAGTC[A/G]TCAGCTTTGTAGTTC | 5607 |
rs192586278 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730873 | ATTAGAATTAGAATT[A/C]GGTGCTACCACAGTC | 5607 |
rs192587602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787963 | AAAAATAATAAGGCT[C/T]TTAATAAAATTGGGA | 5607 |
rs192595343 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686635 | ATAATAATAATAATA[A/T]TAATAATAACATGTT | 5607 |
rs192645189 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597093 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 5607 |
rs192686164 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745662 | AGGAACATAATACAG[C/G]CTTTATGGCAATATA | 5607 |
rs192696010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560864 | GAAGAACTCTCCTTT[G/T]GTTCTTGATTGTGAT | 5607 |
rs192712149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775529 | AATTTGTTAGTTGAT[A/G]TACCATTGTGCACAG | 5607 |
rs192713300 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602110 | TGATTTTTGCGGCTA[A/C]TATTCTCTTTCCCTG | 5607 |
rs192725186 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557038 | TAAAAAATCCTGTGT[A/G]TTTGCATTTCTGGGT | 5607 |
rs192747163 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701164 | AGGAAGGAAAAAAGG[A/T]CAGGGGTTAGGGCAG | 5607 |
rs192748639 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736147 | GCATGGTAGAGGAGG[G/T]AGGTAATGTGTCAGG | 5607 |
rs192773515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697719 | TCAAGGTATAGACAG[A/C]CCAAAATTACCCAAA | 5607 |
rs192785558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732549 | ACATCAAAATGACCT[A/G]AAGTTAAAAAAAGGA | 5607 |
rs192794965 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628882 | TGATGGTGGATATGG[C/T]GGCAGTGGGGATGGA | 5607 |
rs192797120 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593715 | CGATCAAGCCTGCCT[A/G]TTAGGCTGTATTGAC | 5607 |
rs192805416 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765371 | TAATAAAATTTTTTT[A/T]AAAAGTATAGTACAA | 5607 |
rs192813914 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621982 | TGAGATCAGGAGTTC[A/G]AGATCAGCCTGGACA | 5607 |
rs192822191 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654940 | CTCAGTGGTGCATGC[C/T]TGTAATCCCAGCTAC | 5607 |
rs192823928 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696966 | CCTGGGCAACAAGAG[C/T]GAAACTCAGTCTCAA | 5607 |
rs192836143 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556384 | TCTACAGTCCAGGAT[A/G]TTGAAGAAACATTCA | 5607 |
rs192840878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798380 | TGGCACAATTCTGCC[A/G]TTCACAAGGATCAGC | 5607 |
rs192841966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586160 | ATTTGGAATTGTTTT[G/T]TTGGTCAGTGTCTTC | 5607 |
rs192842406 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771278 | TCTACTGCCTGGAGC[A/G]CCTGGTTTGGGCATC | 5607 |
rs192860170 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799591 | TCTATACAAATCTGG[A/G]TTGGAGGATGTATTT | 5607 |
rs192904594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580332 | ATCTGTGCATTTTAT[A/G]CACAAATTGAATAAT | 5607 |
rs192915975 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759753 | ACAGCACATAACTGC[A/G]GGTGGTTAAAGGGAG | 5607 |
rs192922316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793329 | TTATGGACATTGTCT[A/G]TTTGCCATGTTCTAT | 5607 |
rs192951739 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717190 | TGGTCAGTTAAGACT[G/T]CTTTTCATAGGATTA | 5607 |
rs192958395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716563 | AAATTCTCTTATATG[C/G]CTTATGTTGTATTTA | 5607 |
rs192973710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745761 | ACAGTAGCTTTATTT[A/G]ATTGAGAAAATGAAT | 5607 |
rs192980999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641176 | TGTTTTCTAAGTGGG[A/G]AAAATCCATCTAACA | 5607 |
rs192988982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581153 | ATATTTATAAATTGT[A/G]GCTCATGATGGTGGC | 5607 |
rs193000551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680898 | CCCTAGAAGAAGCCT[A/G]CCTTCAGGTGGAGCT | 5607 |
rs193014022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636944 | GCCAGTGTGGCTAGG[A/G]TAAAAGCAGGCAGAA | 5607 |
rs193019387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603675 | TCCCTGGCTTTTAGT[A/G]CAGTGCAAAGAAATG | 5607 |
rs193024178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676449 | CTTGGGACATTTTGC[C/T]AAGCAGAATGGACAG | 5607 |
rs193028708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783276 | AAGCACAGGATAGAA[C/T]GTGAGAATTGCCAGA | 5607 |
rs193057746 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603121 | ACCATATTTAAGTGT[A/G/T]TAGTTAGTGGCATTA | 5607 |
rs193060193 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779818 | GTTATCTTGGATGCA[A/C/G]TAAAGTGGATCAGTT | 5607 |
rs193060480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565387 | GGCACCCACCACCAT[C/G]CCTGGCTAATTTTTG | 5607 |
rs193097347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741735 | ACCAACTGATCATAA[A/G]GAAGAAAACAGGGAT | 5607 |
rs193104701 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660186 | GGAGTAGAAGAAATG[G/T]TTTTTAATAATTTTG | 5607 |
rs193115598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629206 | AGCTACAGGTTACAA[C/G]AGATTTGTGAACTCA | 5607 |
rs193116027 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666193 | GCATACAGGTTAATT[C/G]TGGCTTGTAATGAAA | 5607 |
rs193123853 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705861 | AGGCACCAAGATAGA[G/T]TACACTCTCAGCGTA | 5607 |
rs193124319 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770316 | AGCCTTCTGCCTTTT[C/T]CCTCCTAGCAGAACG | 5607 |
rs193163649 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589483 | CTAAACTACTTAGCT[C/T]TCTCCTTCTGTAAAT | 5607 |
rs193191894 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766840 | AGGCTCTCAGAAAAC[A/G/T]CCTTTGCCCAGTGTT | 5607 |
rs193196679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562964 | TAGTAGAACAAGACT[A/G]GCCTCTCGTTGGTTT | 5607 |
rs193198008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624718 | CATTGCACCGTCTGC[C/T]TCCTGGGTTCAAGCA | 5607 |
rs193200087 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659676 | CTTTGTGGCTTTTGG[C/T]AGTTCTTGGCTGTAA | 5607 |
rs193201478 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699942 | TTTAACCAGTGTTCT[C/G]TCTGCCTACACAGGG | 5607 |
rs193220061 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803601 | CCTGTCTTCCCTCCC[C/T]GGGCCTCAGTGTCCT | 5607 |
rs193221841 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542959 | TGACGAGCGGTGGAC[A/C]CCTGCCGCTGTATCT | 5607 |
rs193233659 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584816 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTAGCTGG | 5607 |
rs193247705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545097 | TTCATTTCTCCCAGG[C/T]GTCCAGGCTGTCTGC | 5607 |
rs193265999 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647744 | GTGTGGTAGCGCATA[C/T]CTGTAGTCTCAGCTA | 5607 |
rs193274811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686277 | TTATAATGACAGATA[C/T]ATCATCCAACAATAA | 5607 |
rs193275939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720948 | ATGTATCACGCTTTT[C/T]AGCATTCATGGTTAG | 5607 |
rs193276312 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753570 | AGAAGATAAACAAAT[A/G]GTCAATAAGCACATG | 5607 |
rs199529382 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715237 | TTTTTTGGGCGGGGA[A/G]GGGGGGGGTCTAAAA | 5607 |
rs199539217 | snp | G/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547186 | CTGTTTATGTCTTTT[G/T]TTTGGTGCTTATACT | 5607 |
rs199548415 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624590 | ACATCACGATCTCTT[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs199551641 | snp | A/C/T | 0.000234285 | 0.0108212 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772775 | AATGTTTTTAGTTAC[A/C/T]TTAGAATTCTCAGTT | 5607 |
rs199568508 | in-del | -/T | 0.021333 | 0.101051 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761749 | CTATGAAAAGATCAA[-/T]TTTTTTTTCATTTAG | 5607 |
rs199600562 | in-del | -/AATAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686604 | TGAGACTGTGTCTCA[-/AATAAT]AATAATAATAATAAT | 5607 |
rs199605852 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624796 | CACCAGGCCTGGTTA[A/T]TTTTTTGTATTTTTA | 5607 |
rs199674502 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563335 | TGATGAGGAAATGAA[A/G]GCAATGCTGTCATAT | 5607 |
rs199695560 | snp | C/T | 1.65455e-05 | 0.00287619 | missense | MAP2K5 | GRCh38.p7 | 15:67769633 | CAGTTGGAGAGTTCT[C/T]GGAGCCATTTGTACA | 5607 |
rs199719473 | in-del | -/GAAA | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570002 | GCCTAAAAATCAGGT[-/GAAA]GAAAGGTCAGTGTGG | 5607 |
rs199757116 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553678 | CAGCACTTTGGGAGG[C/G]CGAGGCAGGTGGATC | 5607 |
rs199759231 | snp | A/C/G | 0.00059288 | 0.0172074 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586823 | GAACACAAGACTGAT[A/C/G]AAGATTCTTTCTTTA | 5607 |
rs199759629 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727014 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCAT | 5607 |
rs199827604 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595989 | TCTTTTTTTTTTTTT[-/T]GTTTTTTAGATTTTA | 5607 |
rs199880386 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565234 | CATCACTGTTATTTA[-/T]TTTTTTTTTCTCCGA | 5607 |
rs199883015 | in-del | -/GC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701172 | AAAAGGACAGGGGTT[-/GC]AGGGCAGCATTTAGT | 5607 |
rs199912214 | snp | A/G | 0.000216024 | 0.0103906 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664686 | ATTTAATTTGGGGTG[A/G]GGTTGGGTCTCTCCA | 5607 |
rs199915671 | snp | C/T | 0.000527391 | 0.0162301 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585863 | TGGCCCTGATGTGTT[C/T]TACAATTTAGTCAAT | 5607 |
rs199918933 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671648 | GGAAAGCAAGAACAC[-/G]TTTTTTTTTCTTTTA | 5607 |
rs199953786 | snp | C/G | 0.00213348 | 0.0325912 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563272 | CATTTGCATTATGTG[C/G]TTTTAAACAGATGAA | 5607 |
rs199977837 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67550050 | ATGTGATAGGCCAGG[C/T]TCTGCCTGAAGCAAC | 5607 |
rs199985122 | in-del | -/CT/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599994 | GAAAAACATGCAAAC[-/CT/TT]TTATATATAAAGTTA | 5607 |
rs200019363 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781350 | TTGTTTAATGGGTTG[A/T]TTGCTTTTTAATTTG | 5607 |
rs200041217 | snp | A/G | 0.000915475 | 0.0213752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646329 | ATTTTTATTTGTAAA[A/G]CATGCCTATGGTATT | 5607 |
rs200075045 | in-del | -/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722366 | TTTTTTTTTTTTTTT[-/T]GGTCCTGCATTACTA | 5607 |
rs200106634 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683756 | CATGAGCAAGACTCT[C/G]TCTCAAAAACAAAAC | 5607 |
rs200121544 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762566 | TTTTAAATGACAGAC[-/AAA]AAAAAAAAAAAAAAC | 5607 |
rs200131196 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790732 | AAAACAAACAAACAA[-/C]AAAAAAAAAAACCTG | 5607 |
rs200154926 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708323 | GCAAGATGCTGTCTT[-/A]AAAAAAAAAAAAATC | 5607 |
rs200159226 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603090 | TGAAATACACATAAC[A/T]CAAGTTAACATTTTA | 5607 |
rs200160236 | in-del | -/TAGGT | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620999 | AATATTAGCAGCTAA[-/TAGGT]TAGGTTGCATTTTTT | 5607 |
rs200178086 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672481 | GAAGTGTCTGTTCAT[A/G]TCCTTCGCCCACTTT | 5607 |
rs200229304 | in-del | -/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623461 | TTTTGCCAGTTCTTT[-/G]TTGTTAAAGCTTTAT | 5607 |
rs200281600 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589781 | AAAATGTGTGTGTGT[A/G]TATGTGTGTGTGTGT | 5607 |
rs200287680 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727019 | GCCTGGCCAACATGG[A/T]GAAACCCCATCTCTA | 5607 |
rs200295613 | in-del | -/ATATTAAT | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658997 | GCAGTCTATGAGAAA[-/ATATTAAT]ATATTAATTTATTAA | 5607 |
rs200297141 | in-del | -/GAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733776 | AGTTAAACATAGGTA[-/GAT]AATAAGTGAAAAATA | 5607 |
rs200323297 | snp | C/T | 1.6554e-05 | 0.00287693 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748552 | AATACTTTTTCCTCT[C/T]TTCTTTTCCATTGCA | 5607 |
rs200458486 | in-del | -/C | 0.0232847 | 0.105357 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682965 | GCCAACACAGCAAAA[-/C]CCCATCTCTACTAAA | 5607 |
rs200459106 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771162 | TTACACATGGTAATG[C/T]GTACCATGTGTTTTA | 5607 |
rs200507054 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575924 | TTTCTTTCTTTTTTT[C/T]TTTTTTTTTTTTTAA | 5607 |
rs200513731 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580533 | CTTAATCAACACTTT[C/T]ACTCTTAAAGATAAA | 5607 |
rs200520298 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589787 | TGTGTGTGTGTATGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs200524660 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683753 | TGACATGAGCAAGAC[A/T]CTGTCTCAAAAACAA | 5607 |
rs200525184 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784725 | TTGGTTTTGGCAAAA[-/A]CTGAGGGCAGAGTGT | 5607 |
rs200558382 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585096 | AAAAAAAAAAAAAAA[A/T]CAAATTAATTCGTCC | 5607 |
rs200574732 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567863 | TGCTTTTTTCCTTCC[A/T]TTTTTTTGTGTTTGT | 5607 |
rs200618305 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619769 | CTTGTTCTACAAAAA[A/T]TAAAAATAAAAATTA | 5607 |
rs200627656 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756516 | CCCACACACAGTTAC[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs200632523 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594329 | AAAATCTGACTAAAA[A/G]CAAAAATATTGAGCC | 5607 |
rs200652843 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543416 | GATCCCAAATAGTGG[C/T]GCGGTGGACTGGACA | 5607 |
rs200655854 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762808 | GTGATGTTCACTTGG[C/T]TAACAGCTGGTTCTC | 5607 |
rs200675078 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599996 | AAAAACATGCAAACT[C/T]ATATATAAAGTTACG | 5607 |
rs200712675 | in-del | -/AA | 0.473634 | 0.111748 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788972 | GAGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 5607 |
rs200735132 | snp | C/T | 4.68966e-05 | 0.00484212 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646282 | CAAATTATGTCTGAA[C/T]TGGAAATTCTTTATA | 5607 |
rs200749839 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741284 | CAGAAAACTCAACTC[A/C]AAGGAGCCCTAATCA | 5607 |
rs200759997 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677608 | ATGTTTTATAGTCAA[G/T]AGGAGTCTTAACAGT | 5607 |
rs200771728 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550376 | CAGGACAAAATGAAA[C/T]GTGTAAACTACCTGT | 5607 |
rs200772764 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589783 | AATGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs200829723 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728292 | TTAAATTCACTTAAA[A/T]TTTTTTGAGTTAAAA | 5607 |
rs200853406 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780285 | ACTTTTTTTTTTTTT[A/T]AACCTTTAAAGTTCT | 5607 |
rs200896459 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622165 | AAAAAAAAAAAAAAA[C/T]AAGATGAAGGGAGAA | 5607 |
rs200920346 | in-del | -/ACACAC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582824 | ATACATTGTCTCAAA[-/ACACAC]ACACACACACACACA | 5607 |
rs200920640 | in-del | -/ACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756570 | GTGTGTGTTGATAAC[-/ACTT]ACGATCTACTCCCTT | 5607 |
rs200944611 | snp | A/G/T | 0.00021561 | 0.0103808 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563262 | CACACCTTATCATTT[A/G/T]CATTATGTGCTTTTA | 5607 |
rs200980828 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654463 | CATATAGTTGGATCA[-/T]TTTTTTTAAAAATCA | 5607 |
rs201013151 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805603 | GGAGGGAGGAGAGAG[C/T]TGGGGGGAGCGAGGA | 5607 |
rs201015322 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621434 | AATGAACAAAAGTTT[A/G]AAAAAAAAAAAAAAA | 5607 |
rs201034391 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703893 | TGTTTGTTTTAAAAG[-/A]AAAAAAAAATCACCT | 5607 |
rs201063917 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752690 | TCAAAAAAAAAAAAA[-/A]GAAAAAGAAAGAAAG | 5607 |
rs201104467 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614933 | CAGTTATCTTGAAAT[G/T]AATATCTGTGACCTC | 5607 |
rs201111316 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727050 | CTAAAAATACAAAAA[C/T]TAGCTGGGCATGATG | 5607 |
rs201130138 | in-del | -/TTAC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756572 | GTGTGTTGATAACAC[-/TTAC]GATCTACTCCCTTGG | 5607 |
rs201132626 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709479 | TCAAGACTTCAGGGC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs201144707 | in-del | -/C | 0.190519 | 0.242821 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612076 | TCTTTGGTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 5607 |
rs201155786 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687977 | GAAGAAAAGGGAAAG[A/G]AAGTATCTGAGCTGG | 5607 |
rs201160887 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608190 | CCTGCCACACCAAGA[A/T]GGCATAACATCAGGG | 5607 |
rs201165206 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678962 | AGTGACACTGCATCT[A/C]AAAAAAAAAAAAAAA | 5607 |
rs201172954 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580756 | AATCTCTTTGCAGTA[C/T]TATTCCACAGTAATG | 5607 |
rs201179837 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567703 | GAAATGCTTTATTAG[-/A]AAAAAAAATACACAC | 5607 |
rs201198413 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793282 | TGAGACCTCATCTCT[-/A]AAAAAAAAACAAAAA | 5607 |
rs201205437 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595991 | CTTTTTTTTTTTTTG[G/T]TTTTTAGATTTTATA | 5607 |
rs201211067 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621057 | AGACTGTATTGGGAG[-/A]AAATTTAAAATACCA | 5607 |
rs201215088 | snp | A/T | 0.00044599 | 0.0149264 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692574 | CTCTTTTCCTCCCAG[A/T]GTACTGTTTTCTCTG | 5607 |
rs201260164 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580537 | ATCAACACTTTTACT[C/T]TTAAAGATAAATGCC | 5607 |
rs201260832 | in-del | -/TC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612075 | ATCTTTGGTTTTCTT[-/TC]TTTTTTTTTTTTTTT | 5607 |
rs201270061 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660884 | GAGAAAAAAAAAAAA[A/T]AGAGGCAGGAGTGGA | 5607 |
rs201325124 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615690 | TAAAAATTTAAATTT[A/T]TTTAATTTAAAATTT | 5607 |
rs201342447 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771163 | TACACATGGTAATGT[C/G]TACCATGTGTTTTAC | 5607 |
rs201384632 | in-del | -/TTACAGT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700968 | TGCTTTATTATCAGC[-/TTACAGT]TTGCATTTGTTTTGA | 5607 |
rs201446724 | snp | A/G | 9.89838e-05 | 0.00703435 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580739 | GAGTGATCTCTTTCT[A/G]TAATCTCTTTGCAGT | 5607 |
rs201457162 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759395 | AGACCCGATCTCTAC[-/A]AAAAAAAAACAAAAA | 5607 |
rs201544290 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624590 | ACATCACGATCTCTT[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs201547356 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603091 | GAAATACACATAACT[C/T]AAGTTAACATTTTAA | 5607 |
rs201575748 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572706 | GATATTATTATTATT[-/A]TTTTTTTTTTTGAGA | 5607 |
rs201600736 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621063 | TATTGGGAGAAAATT[C/T]AAAATACCAAGACAC | 5607 |
rs201621976 | snp | C/T | 4.98128e-05 | 0.00499038 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563257 | AAATGCACACCTTAT[C/T]ATTTGCATTATGTGC | 5607 |
rs201636416 | snp | A/G | 0.000150264 | 0.00866657 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646403 | TGCGATTCATCATAT[A/G]TCATTGGATTTTATG | 5607 |
rs201661333 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572707 | ATATTATTATTATTA[-/T]TTTTTTTTTTGAGAT | 5607 |
rs201661639 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589789 | TGTGTGTGTATGTGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs201677717 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597509 | GTCTTAGAATGCTGT[-/A]AATTTCTGTGATTTT | 5607 |
rs201761109 | snp | C/G/T | 6.58939e-05 | 0.00573962 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586826 | CACAAGACTGATCAA[C/G/T]ATTCTTTCTTTACTT | 5607 |
rs201774361 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595989 | TTCTTTTTTTTTTTT[G/T]GTTTTTTAGATTTTA | 5607 |
rs201781403 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760430 | TAAAATTAGATTTTA[C/T]TAACTATTGCTGAAA | 5607 |
rs201909124 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683754 | GACATGAGCAAGACT[C/G]TGTCTCAAAAACAAA | 5607 |
rs201920307 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605873 | TATCTAGCTACTTTG[C/T]GAGGCTGTACAATTG | 5607 |
rs201944586 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621059 | CTGTATTGGGAGAAA[-/T]ATTTAAAATACCAAG | 5607 |
rs201945284 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615184 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 5607 |
rs201962578 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586895 | GCCCAGCAGTCTCAG[A/G]TTCACTTCCAAGCAA | 5607 |
rs201971878 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726493 | ACTAATAAAATGAAA[-/A]TAGGTATTCTGTTAA | 5607 |
rs202001400 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655064 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 5607 |
rs202006677 | in-del | -/AGAGTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643469 | TTTTGAGACAGAGTC[-/AGAGTC]TCGCTCTGTTGCCCA | 5607 |
rs202010303 | snp | C/T | 0.00227722 | 0.0336664 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658538 | TGTAGTAACATGGCA[C/T]GTTTATCTCTACAGG | 5607 |
rs202013279 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629699 | CCTATCCTAACACTT[A/T]CCAGATGAGAGGAAG | 5607 |
rs202017530 | in-del | -/TA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572707 | TATTATTATTATTAT[-/TA]TTTTTTTTTTGAGAT | 5607 |
rs202027046 | in-del | -/ACAT | 0.00199481 | 0.0315187 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720296 | TATACATAAGTATAC[-/ACAT]ACATACACACACATA | 5607 |
rs202055624 | in-del | -/ATGAGGGG | 0.0244538 | 0.107838 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614978 | TGAGACCTAAACAGT[-/ATGAGGGG]ATGAGGGGCTCTGTT | 5607 |
rs202074012 | in-del | -/GCC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578221 | TTCATTCATGTGCCT[-/GCC]TGCTCATCTCACTGA | 5607 |
rs202104621 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572709 | ATTATTATTATTATT[A/T]TTTTTTTTGAGATGG | 5607 |
rs202181519 | in-del | -/T | 0.392881 | 0.205147 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722352 | ATTAATTTGTAACTC[-/T]TTTTTTTTTTTTTTG | 5607 |
rs202188275 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688386 | GAACACAAACTATAA[C/T]AGAGCAAGTGTAAAA | 5607 |
rs202194867 | snp | G/T | 1.65861e-05 | 0.00287972 | missense, intron-variant | MAP2K5 | GRCh38.p7 | 15:67664607 | TTTAGGTTGTTAAAG[G/T]CCTTACTTATTTGTG | 5607 |
rs202238954 | snp | C/G | 0.00697557 | 0.0586441 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641449 | TTTCCCTTTAGTGAA[C/G]TGTGTGCCACTCCAG | 5607 |
rs202246966 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622541 | TGGATTTTTTTTTTT[-/T]GTAAAACACTATCCA | 5607 |
rs207475571 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743960 | ACTCCAAAGTTCATG[C/T]GTTTTCCTCACAGTG | 5607 |
rs367551663 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734582 | AAGCCTTTGACTAGT[A/G]TATTGTTACTAATTC | 5607 |
rs367555045 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684541 | GATTCACAATGTTGA[A/C]AATCCAAATAAAAAG | 5607 |
rs367600988 | in-del | -/TGATAGTCCCATCTTGGCCTTTCA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552697 | CATCTTGGCCTTTCA[-/TGATAGTCCCATCTTGGCCTTTCA]AAGTGCTGGGATTAC | 5607 |
rs367602802 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565709 | TTAGTTTAAAAGTTT[-/T]CTGAGATTACTTGGG | 5607 |
rs367618551 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805909 | CCAGGAGGCCCTAAG[A/T]TTGTGGATGTAAATC | 5607 |
rs367641191 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635825 | GAGAAGTTTACTGTC[-/A]TTTTAAATCTTTGTT | 5607 |
rs367648517 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630374 | TTGTAGTTATTTCAC[C/T]ATATCTGTTACTTTG | 5607 |
rs367663431 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585670 | CAGAAATTGGAATTT[A/G]TATGAGGTGGTGTCA | 5607 |
rs367667032 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567522 | GGCGCCCGCCACCGC[A/G]CCCGGCTAATTTTTT | 5607 |
rs367669981 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542638 | CGCGGGAGGCGGGTC[C/T]CGCTCGTCGGCTCCC | 5607 |
rs367678722 | in-del | -/CA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711692 | ACACACACACACACA[-/CA]AAAGGATAATACCAT | 5607 |
rs367688027 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621100 | ATTGAAAGGAAAAGG[A/G/T]TAGGGGAAGATACCT | 5607 |
rs367780480 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774076 | ATGGATGTATATGTT[A/G]GTAAGGAACACCACT | 5607 |
rs367797824 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768094 | TTTGTTTGTTTTTTG[G/T]CTGCCTTGACCCCCT | 5607 |
rs367800796 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594764 | TATGGCTTTTTTTTT[C/T]TTTATAAGGATTAGC | 5607 |
rs367818715 | snp | A/G | 8.27931e-05 | 0.00643348 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692429 | TTTTAAAGAACAAAC[A/G]CTGTAGATACATGGA | 5607 |
rs367826801 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601625 | TGTATTTCCAGAGTT[-/G]TAAAATAATTAACTT | 5607 |
rs367827973 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692408 | TGGTGTGGTGTGCAT[G/T]TGTGCTTTTAAAGAA | 5607 |
rs367846356 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681924 | ATTAAACCAAAATGA[C/G]TTACATCTGCCCTGA | 5607 |
rs367853724 | snp | G/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672002 | TGAACTCATCATTTT[G/T]TATGGCTGCATAGTA | 5607 |
rs367897752 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756062 | CTCCCCCACACTAGG[A/G]CACAAAGGCCCTTTT | 5607 |
rs367905621 | snp | G/T | 1.65334e-05 | 0.00287514 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692583 | TCCCAGTGTACTGTT[G/T]TCTCTGCAACAACCC | 5607 |
rs367917639 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553793 | TGGCGGGCGCCTGTA[A/G]TCCCAGCTACTCGGG | 5607 |
rs367925472 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634174 | GACCAGCCTGGGAAA[C/T]GTGGCAAAACCCTGT | 5607 |
rs367973577 | snp | C/T | 6.60175e-05 | 0.00574494 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563337 | ATGAGGAAATGAAGG[C/T]AATGCTGTCATATGT | 5607 |
rs367991311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762886 | TTCAGGCCTTTACCC[C/T]GTGGTTCCAGGCCCA | 5607 |
rs367991445 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777416 | TAATCAGGTCAGAAG[A/C]AGCAGCATCCCGGTT | 5607 |
rs367991592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802980 | TTGGAGTCGGAGACC[C/G]ATGTTCTGGTTCTAG | 5607 |
rs367992728 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721829 | ACTTTTAATGATGGT[A/G]TCTTTGAATTTCCTT | 5607 |
rs367996110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696096 | CCCTGACTTTTATCT[A/G]CTGACAGTCTCTTGA | 5607 |
rs368008524 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556633 | CTCAGCTCACTGCAA[C/T]CTCCGCCCCCTGGAT | 5607 |
rs368011912 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670000 | TTTAGGCAACTCTTT[A/G]TAGTGGCTTTATTCA | 5607 |
rs368034217 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706639 | TGAGCACCTCTGTAC[A/G]TGATGCTTAACTAAA | 5607 |
rs368037077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751480 | ATACCTGCGTTGTAA[A/G]GTGCTTTGGTTCTTT | 5607 |
rs368038340 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622201 | TGAAGGGAGAATGTG[C/T]TGTTTTATGTAGGAA | 5607 |
rs368040155 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638214 | TTTTCCTGATCATCT[C/T]CCCACTTCACCCTCC | 5607 |
rs368054869 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795385 | ATGAACTTGCCTGCT[A/G]ATATTGCTTTAGCTG | 5607 |
rs368069093 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631090 | TTCAGACACCTGAAG[A/G]TCTTTTAAGTATGCC | 5607 |
rs368085484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734772 | AACTTTTTGAAGTTT[A/G]GAACATGAAGGATTT | 5607 |
rs368087520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761892 | ATGCCAGTGTGTATA[G/T]TAACATTATAATTTA | 5607 |
rs368106577 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767156 | TGAGGAACTTAACAG[C/G]CTACAATATCAGGTC | 5607 |
rs368107660 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781589 | CATTTGCTGGAGTGT[A/G]GACTAGTTTCTTTCC | 5607 |
rs368117363 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585775 | GGGAGCCACTTTTCA[A/G]TCATTTCTCTCTGCT | 5607 |
rs368130338 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649342 | TTGTTTATCTTTTCA[C/T]TTTCTTTTTTCTTTT | 5607 |
rs368159271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586654 | GGAATAATGACAGGA[A/G]TAGAATATTATGTAA | 5607 |
rs368177779 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719786 | TGTTGCATTTTGAGC[G/T]ATGCAAACATTTGAA | 5607 |
rs368216800 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801698 | TCAGGAGAGCTGTGG[G/T]CAGATGTAAGGCATT | 5607 |
rs368236864 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602498 | TCACCAAACCTTTAG[C/T]TTTATATTAATTGAA | 5607 |
rs368240385 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572948 | TGATCTGCCTGCCTC[A/G]GCCTGCCAAAGTGCT | 5607 |
rs368240673 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781081 | CATGCCACCCACTCC[C/T]CAGCTCTTGGGAATA | 5607 |
rs368250836 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672159 | GCAGCATGATTTATA[A/G]TCCTTTGGGTATATA | 5607 |
rs368310392 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554333 | CAAAGTGTTGGGATT[A/T]CAGGTGTGAGCCACC | 5607 |
rs368311459 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573539 | TCCTCCAATTAAACA[A/T]GAGATTTGTGGGCGG | 5607 |
rs368313400 | snp | A/C | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661768 | TGGTGAGCTATCTTT[A/C]ATGGATAGTTTTTAT | 5607 |
rs368346726 | snp | A/G | 1.65375e-05 | 0.0028755 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748645 | CCTAAAGTCATTCCT[A/G]ATGGTGTGGAAAGCT | 5607 |
rs368398438 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742617 | AAAGGAGAAAAGACT[A/G]ATATGGCAAATGTCT | 5607 |
rs368422802 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567405 | CTCTGTCGCCCAGGC[C/T]GGACTGCGGACTGCA | 5607 |
rs368436825 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703457 | ATCTGTACTAATATA[A/T]TCAATCAGGAAAAGT | 5607 |
rs368441009 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609344 | TAGTGGGGCAAACAA[C/T]AATCAAGACAATAAA | 5607 |
rs368441140 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67664112 | CATTAAAGGTAGGAA[C/T]CTGTGGCTTTTGCAT | 5607 |
rs368455000 | snp | A/G | 5.03732e-05 | 0.00501837 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592963 | CTGAAAAAAATACTA[A/G]CCAATGGCCAGGTAG | 5607 |
rs368455854 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576001 | CTCGGCTCACTGCAA[C/G]CTCTGCCTCCTGGGT | 5607 |
rs368468528 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574157 | CTCAAGAGTGGCTTG[A/G]GGTAGAGAATTTATG | 5607 |
rs368468834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689102 | CTTAGTATAAAATGT[C/T]GTTAAAGCTGAGTGC | 5607 |
rs368477945 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622853 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGTCGAGG | 5607 |
rs368492275 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704781 | GTGTTTTTGATTTGT[G/T]GGACTCAGTATTGCT | 5607 |
rs368495839 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591788 | AGCTAGATGACTTAA[-/G]AGCTCCCCTTGACTA | 5607 |
rs368503375 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751693 | GAGTGTGGTGAATAT[C/T]ATTTAACCTTTTCTC | 5607 |
rs368512067 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668513 | CTGTTAGGCCAGATC[C/T]GACATTACAGGAAAC | 5607 |
rs368514078 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629222 | AGATTTGTGAACTCA[A/G]CCAAGCACGGTGGTG | 5607 |
rs368515921 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758618 | TCAACACTTTTTTTT[-/T]CAAGACCTCAGAAAT | 5607 |
rs368518209 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648331 | GAATCTGATAATATA[C/T]GGCCTTTGTGTCTGG | 5607 |
rs368521983 | snp | A/T | 0.000101025 | 0.00710651 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600639 | TTCCTTGACATTTCC[A/T]TCCACAGCATGACAC | 5607 |
rs368545957 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559500 | AATTGCTAACAACAT[A/G]TGGCCTGTTATGATT | 5607 |
rs368578387 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587021 | TAGATAACCTAGCTA[C/T]GTATTGACCAAAGAG | 5607 |
rs368651799 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571407 | TTATTTATAGTACTG[C/T]AGTAATTGAGGGGAA | 5607 |
rs368660723 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734012 | TTTGCAAATGCTTTT[C/T]GATTACCAATAACAT | 5607 |
rs368668068 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754230 | TTGTTACTTTAAAAG[G/T]GTGAATTTTATTTTT | 5607 |
rs368673691 | snp | C/T | 1.71164e-05 | 0.00292539 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664556 | GTTCCTTTTAAAAAC[C/T]ATAATTGATAATTGT | 5607 |
rs368675285 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659822 | TCTGCCATCTTCAGT[A/G]GAGAAGCATGTTCTT | 5607 |
rs368691006 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574129 | TAAGGATCCCTTTCT[C/G]ATAACAGTATTTCTC | 5607 |
rs368692138 | in-del | -/ATTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687345 | GCTTAGGAGCTATTT[-/ATTT]GCATAACTTTCATTG | 5607 |
rs368701124 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766979 | GGCATTGTGCATGTG[A/G]GATTAGAATTTCCCC | 5607 |
rs368708063 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725025 | CAGGAACATAGTTAA[A/G]AGGTAGGACTGAGGT | 5607 |
rs368710599 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587100 | GAGAAGGCTCTCTGG[A/G]GAGAGTGACGTTTCT | 5607 |
rs368714175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691831 | CAGCAGCCAAAAATA[A/G]TGTAAGGGAAGAGAA | 5607 |
rs368718348 | in-del | -/ACAC/ACACACAC/ACACACACACAC/CACAC | 0.473634 | 0.111748 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547077 | TCAAAAAAGAAGAAA[lengthTooLong]ACACACACACACACA | 5607 |
rs368719700 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648712 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 5607 |
rs368720012 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653012 | ATTAGTTTTTTTATT[A/G]CCAACTCAATCTCTT | 5607 |
rs368722566 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708200 | TGGTGGTGTGTGCCT[A/G]TAGTCCTTGCTATGT | 5607 |
rs368733195 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805851 | CTGTGGCCTGGTAAC[C/T]CTGGGGTTGTCCCTG | 5607 |
rs368748168 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545107 | CCAGGTGTCCAGGCT[C/G]TCTGCACTCTGCTCT | 5607 |
rs368758583 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554774 | AATGAGCTTGCTGCC[C/T]TAGAGGAACACACTT | 5607 |
rs368780139 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797122 | CCTTACCGCAGCCCC[-/T]TTTCCCCCAGACTTC | 5607 |
rs368796354 | snp | C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547455 | TCGGTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 5607 |
rs368829947 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735770 | TAATCAGTTTAGCCC[A/G]GAAATAGAATAGAAG | 5607 |
rs368841407 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794834 | AAGGAACTAGAAAAA[C/T]TGTTACTAAGATTTT | 5607 |
rs368858521 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748113 | CATTATGTAAATTGT[A/G]TTAACACATGCCCAC | 5607 |
rs368870377 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805221 | TCTGAGATAGACCCA[C/T]GCAGGGTGTCCCCAG | 5607 |
rs368872390 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784639 | AGGAAGTAATTACCA[A/G]CAGTTTGCACCTGGT | 5607 |
rs368877843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572540 | CTACTTTCGGGAACG[C/T]CCTACTCTATGGAGT | 5607 |
rs368895285 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697570 | AAGATTTATTCTGCT[C/T]ACTCTATATATCCAG | 5607 |
rs368899265 | snp | A/G | 5.08203e-05 | 0.00504059 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592908 | ATCTTGCCACTAAAA[A/G]TTATCTTTCCTTTTC | 5607 |
rs368902366 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639302 | TCTTTCTTGTCAGAC[A/G]TGTATACCAGCTTTT | 5607 |
rs368905056 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671002 | GAAGGAATAAGGCTT[C/T]ATCTGACATTCCCAA | 5607 |
rs368927610 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570176 | CTGCTATTGGCTGCC[C/T]AAACTTCTATGAAGG | 5607 |
rs368928374 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562088 | AAAAATAATAATTCC[C/G]ATTGTTAACACCAGA | 5607 |
rs368979378 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572092 | AATCTAGCTTTGGGG[A/G]CCAAAAAGGCTTCCT | 5607 |
rs368980711 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786020 | AGCTGTTAGGTTGTT[-/G]TTTTTTTTTTTAACT | 5607 |
rs369005394 | snp | C/T | 0.000159987 | 0.00894249 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806684 | CAATGATGGAAATGC[C/T]GCCGTGGTGTCCATG | 5607 |
rs369012614 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791016 | ACCACAGGTAAATTA[C/T]TACCTGTCTACCCAG | 5607 |
rs369017443 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650432 | TTTCAGTCTTTCACC[A/G]TTAAATATGATGTTA | 5607 |
rs369044926 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765414 | AGATAGAAAATTGTC[A/G]TAGATACAAGACACA | 5607 |
rs369047415 | snp | C/T | 3.32209e-05 | 0.00407546 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769671 | ACTCAGTGGTGAGCC[C/T]GTTTACAAACATGCC | 5607 |
rs369050562 | snp | A/G | 0.000100276 | 0.0070801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563393 | TTTTAAAATCTTAAC[A/G]TGATTGAGGATGCTG | 5607 |
rs369053729 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644319 | GAATGGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 5607 |
rs369059397 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618423 | TGTTTAATTCACTTC[C/T]TAAGTGAGCGTGTGT | 5607 |
rs369082688 | snp | A/C/G | 3.3278e-05 | 0.00407898 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693482 | TTATTTCCACATTAT[A/C/G]TTTATATTGTTCTAA | 5607 |
rs369114999 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762565 | CTTTTAAATGACAGA[-/C]AAAAAAAAAAAAAAA | 5607 |
rs369155851 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686199 | CCAATTAAAAGCACA[A/G]ATGTCAAACTGTATA | 5607 |
rs369160720 | snp | C/T | 0.000115406 | 0.00759537 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585853 | AATTTGTAAATGGCC[C/T]TGATGTGTTCTACAA | 5607 |
rs369179251 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574622 | ATCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 5607 |
rs369184365 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726502 | AATGAAATAGGTATT[C/T]TGTTAATTGAAATAA | 5607 |
rs369185025 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678405 | CATTGTCATCCCACA[A/C]CAGCCACATGCCACA | 5607 |
rs369201193 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744494 | CATAAATCTTCCAGA[A/C]AAGAGCTGCAGGGCA | 5607 |
rs369203102 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763764 | AACAGTGGAGGATCA[A/C/G]AAACCAATTTAGGGT | 5607 |
rs369218433 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632114 | TTTTTTTTTTTTTTT[G/T]ATTGAGACAGGGTCT | 5607 |
rs369236297 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641184 | AAGTGGGAAAAATCC[A/G]TCTAACAGGAAATTT | 5607 |
rs369239317 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624149 | TCGAGACCATCCTGG[C/G]TAACACAGTGAAACC | 5607 |
rs369245538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660429 | AATTGATGGGCTGTG[A/G]GCTGTGGTGTGTAAA | 5607 |
rs369258676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560333 | TTTCTAACTCAGTTT[C/T]CTCTTGGACAAAAAC | 5607 |
rs369263745 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777539 | TTCGGCTGTGGTAAA[A/T]GTACGTATCACATAC | 5607 |
rs369265222 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723324 | AAATTATAAAATCCA[A/G]CATATTCAAATGCTG | 5607 |
rs369267118 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698178 | TATTAAATTAACCAT[A/T]TTTCAGAAATTCTTT | 5607 |
rs369267206 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800321 | AGTGGGGTTTTTTTT[-/T]AGCATGAATGTATTA | 5607 |
rs369270363 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735974 | CAAAGGAGGTTCATC[A/T]GGTAAAAGATAAAGG | 5607 |
rs369281164 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799190 | AAAAAATAATAAAAA[C/T]AATAAATCAGAGGCC | 5607 |
rs369286082 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600180 | TTGCAAAGAAAAGCT[A/T]TATCTACTCTAGGAA | 5607 |
rs369287854 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627270 | AAGTTTTATAAGTAG[C/T]ATTTAGAAATAACCA | 5607 |
rs369312740 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555301 | TGGAGGAGGTGCCAG[C/G]CTCCTTCAACCAACC | 5607 |
rs369325807 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567625 | CGCCTCGGCCTCCCA[A/G]AGTGCTGAGATTACA | 5607 |
rs369348672 | in-del | -/GA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701439 | ATAGACTAGAAAACA[-/GA]TGATTTTACAACACA | 5607 |
rs369349047 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582825 | TACATTGTCTCAAAA[A/C]ACACACACACACACA | 5607 |
rs369351620 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668347 | GTGTGATAATTCCAC[-/AT]GAGGACATAATCATT | 5607 |
rs369353989 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691130 | TCAACCACAATGTGT[A/G]CTTGTGGTTTCCATT | 5607 |
rs369356913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643796 | TTTTTCCCCACCTTC[C/T]GCTTCCCCAAATCAA | 5607 |
rs369361679 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613108 | CCAATCAATAGGTGA[C/T]TGAAACTGATTAAAA | 5607 |
rs369386921 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643433 | CTGAGATCTTATAAA[-/A]TAACCCCAAAGCAAA | 5607 |
rs369388377 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803878 | CAGGAAGAGCCCAGG[C/G]CAGTGGGTTTGGGTT | 5607 |
rs369408206 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649014 | ATTCATACCAGCACT[A/C/G]TATAAGGTTCCATTT | 5607 |
rs369429159 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656418 | CAACCTTCACCTCCC[A/G]GGTTCAAGCAATTCT | 5607 |
rs369432814 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782344 | ATTAAGGCAAATCTG[C/T]CGATGTAAACAAAAT | 5607 |
rs369453982 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673482 | TTATTAAATGGGAAA[A/T]GAGAAATGGTTTGGT | 5607 |
rs369456065 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778518 | GTAGGGAGAGTGTTT[A/G]TTAATGAGGAATGGC | 5607 |
rs369481296 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669661 | GGATATATTTTAAAT[A/G]TATAGTTGATAGAAT | 5607 |
rs369514957 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557647 | TAGTATGACCATTTA[A/C]AGCTAAATTGCAATT | 5607 |
rs369538177 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627635 | ATGCTCTTAATAACT[A/C]AATCATTTCTATAAG | 5607 |
rs369546612 | snp | A/G | 8.24015e-05 | 0.00641825 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585935 | ATGGCCTGAAGGTAC[A/G]AATTTCAATAATTGT | 5607 |
rs369579494 | snp | A/G/T | 5.65652e-05 | 0.00531789 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593005 | TATTAAGATTTTCAC[A/G/T]TAATAATAACATATT | 5607 |
rs369601076 | in-del | -/T | 0.381308 | 0.21274 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623598 | AACTTACTATCTTCC[-/T]TTTTTTTTTTTTTTA | 5607 |
rs369612381 | in-del | -/TGTT | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779247 | GCCATTAAAATCATC[-/TGTT]TGTGTCTGCTTATAA | 5607 |
rs369628054 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758550 | CCTAGTACTGCACCT[A/G]ACATCCTATAGGCTC | 5607 |
rs369636827 | in-del | -/AATAAGCATACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769854 | ATTTACACAAAGGGT[-/AATAAGCATACTT]CATAAGCATACTTCA | 5607 |
rs369642197 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795961 | TTTTGTCTTTATGAG[C/G]TGATTCTATCTCTAA | 5607 |
rs369666636 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642128 | CACAAATACAGTATT[-/T]CCTTACTACATTTTA | 5607 |
rs369673690 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707901 | TACTTTTTTGTGTGC[A/C]TGCCTTCTTCAAAGT | 5607 |
rs369673989 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600665 | GACACCCTTTTTGTT[C/T]TTCTTTCTTTCTTGT | 5607 |
rs369674601 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729369 | GTAGAAAACTTATAA[A/G]CCATCCAGTAAAAAT | 5607 |
rs369678900 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651599 | TTTGTTTTTGGCTCC[-/C]ACATGTGAGTGAGAA | 5607 |
rs369701055 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789606 | GTAATTCCAGCTACT[C/G]TGGAGACTGAGGCAG | 5607 |
rs369704608 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620717 | TTGATTGAAGTTAAA[-/A]CATTCTAAGATTTTT | 5607 |
rs369727516 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613477 | TATTATCTCATAAGC[A/G]AGATGAATGCTTGAG | 5607 |
rs369731458 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588485 | GCACATTGTATTATA[A/G]TCACCCCTGTCCTCC | 5607 |
rs369731980 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610329 | CCTTTGGGTGTCCTT[A/G]TTTACCAAAAACTTA | 5607 |
rs369735852 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649725 | ACACCATATTTGATT[A/G]CTTGTACTTGAAAAC | 5607 |
rs369775303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546900 | CAAAACCCCATCTCT[A/G]CAAAAAATGCAAAAA | 5607 |
rs369780854 | snp | A/G | 4.94662e-05 | 0.00497299 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543329 | ATGTGAGCCTCTTTA[A/G]CCTGTAATGCTGTGG | 5607 |
rs369781588 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578250 | GAGCAGCATGGACCT[G/T]GTGGCCGGTCAGGAC | 5607 |
rs369793781 | in-del | -/T/TT/TTT | 0.189261 | 0.242509 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650515 | TTCTAGTTTGTTGAG[-/T/TT/TTT]TTTTTTTTTTTTTTA | 5607 |
rs369824860 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758833 | GGTTCCTTACATTAT[A/G]CTATCACTGATTTGA | 5607 |
rs369828327 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587969 | AGATCACTGCCACAG[C/T]CTCCTGAGAGTCTAC | 5607 |
rs369831694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738713 | TACACACAACCACAC[A/G]AGCAGCTCTGCTTCT | 5607 |
rs369834539 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575916 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 5607 |
rs369849912 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618306 | TTGGGGTCTGTTGTT[-/TT]AGCTTACTGTTTGTA | 5607 |
rs369870465 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698698 | TAAATAACCATTCTT[A/C]TCTCTAGAACATTTT | 5607 |
rs369874465 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757249 | CCATCCTAACAAAAT[G/T]TGAGGTGACATTTCA | 5607 |
rs369881311 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769015 | TCCTTAATTCACTGG[C/G]TTTCTCATATGAGGA | 5607 |
rs369888478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775914 | GTTCAAACAGGCAAC[A/G]TATTCACCACCAGCT | 5607 |
rs369895912 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804719 | TGTGTTACCCCGGGC[A/G]TGGGGGGAGGGGCCC | 5607 |
rs369920911 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628124 | GAGAGCTGTCTCAAG[A/G]GGAGATTCTCAAAGA | 5607 |
rs369934366 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610608 | TAACTTTCTGCCACA[G/T]TTTTTTTTTCTTTGC | 5607 |
rs369941018 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605106 | TCGCCAGGCTGGAGT[A/G]CAGTGGAAAGATCTC | 5607 |
rs369942237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623749 | ATTACAGGCACCCAC[C/T]ACCACACTGGGCTAA | 5607 |
rs369944680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666400 | AATTTTTACTCTGGG[C/T]TTGGGAGAAATAACT | 5607 |
rs369949717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572302 | TAGACCATGGAGGGC[C/G]TTAGCCCAGGGAAGT | 5607 |
rs369953687 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693947 | TCTTGGAATATGAAC[A/G]TGCTTTGTCACCAGA | 5607 |
rs369954085 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645750 | TAGAGATGGGTTCTC[A/G]CTATGGTGCTTAGAC | 5607 |
rs369963694 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | MAP2K5 | GRCh38.p7 | 15:67727935 | CTCTTGGGAGGTTTC[C/T]ATATCCTCAGGTAAG | 5607 |
rs370004847 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597399 | CTCCATACTTAATAC[C/T]GGAGACAAACTGCTG | 5607 |
rs370012889 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736635 | ATTCACAATCACCAT[A/G]TAATATATAGAATTA | 5607 |
rs370020494 | snp | A/G | 0.000519413 | 0.016107 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806608 | TGAGCGCGGGAGTCC[A/G]AGGACTGCCTGTCAC | 5607 |
rs370025354 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755659 | ATGATTCTTTTTAGT[A/G]CCACCATAATGATGT | 5607 |
rs370039700 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655440 | AATTTCCCAGTTTAT[A/T]TGAGAGTATCTTAAT | 5607 |
rs370052607 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671961 | AATGATGATTTCCAG[C/T]TTCATCCATGTCCCT | 5607 |
rs370054520 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584908 | TCACCATATTGGCCA[G/T]GTTGGTCTTGATCTC | 5607 |
rs370065701 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740605 | CTCAACAAAAAAAAA[-/A]GTGTTTCCTTTTCAG | 5607 |
rs370070469 | in-del | -/TATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589789 | GTGTGTGTATGTGTG[-/TATA]TGTGTGTGTGTGTGT | 5607 |
rs370078643 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783588 | TGCACTCGTCACGCT[C/T]TGTGGCAGTAACTTG | 5607 |
rs370085676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785493 | TATCAGACACTAATC[C/G]AGCAAACACAAATCC | 5607 |
rs370092993 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600792 | CTATCCGCTTTTCCA[A/G]ATACTGAGTATCCAA | 5607 |
rs370104122 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635225 | GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 5607 |
rs370134584 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566062 | TTATTTTGTAGGTTC[A/G]ATTTGGCTCTGAAGT | 5607 |
rs370157442 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602799 | GTTGGGATTACAGGC[A/G]TACGCCACCATGCCC | 5607 |
rs370160770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629962 | ATTTAAACATAAAAG[A/G]TACGGTGGCTCACTC | 5607 |
rs370185442 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661066 | AGGCAGGTTCATAGG[G/T]CCAAGGTTCATTACA | 5607 |
rs370187987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786166 | GGGTATTTCCAGCTT[G/T]TTGCCTCTTGGAAGA | 5607 |
rs370212218 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748565 | CTCTTCTTTTCCATT[A/G]CAGCCTCTCCAGCTT | 5607 |
rs370216158 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780199 | AGAGTTACCTCAGAG[A/G]TTTAAAAGGCTAAAG | 5607 |
rs370239633 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589073 | TAGTCTCAAACTCCT[C/G]GCTCAAGCAATTTTC | 5607 |
rs370268205 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639419 | CACAACATTTTGTAA[C/G]TCTTACTGATTCCTG | 5607 |
rs370279354 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581871 | GAATCAGGAGTGCTT[A/G]GTATATTACTAGTAA | 5607 |
rs370288440 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554512 | TGTAGAGAAAAAGAG[C/T]TGAGTGAGTGGAAAA | 5607 |
rs370294486 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759559 | AGCGAGACTGTGTCT[A/C]AAAAAAAAAAAAGAA | 5607 |
rs370294661 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646079 | GGTTAGACAGATGCA[C/G]ATACAGCTTGTATTA | 5607 |
rs370307969 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653114 | TAATCTGTTTCATCT[A/T]GGTTATCTAATTTAT | 5607 |
rs370350430 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769351 | CCTACCCTGTGGCTA[A/T]CATTGTCCTTTTTTC | 5607 |
rs370375131 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646365 | GCAGGTTTATAACTA[C/T]TTTTGTCTTATTTTT | 5607 |
rs370376340 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586860 | GGTGAATACTCGGGC[C/T]GGACCCTCTCAACAC | 5607 |
rs370381867 | in-del | -/A | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682678 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG | 5607 |
rs370396731 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684038 | GAATTTGGAGTTCAA[G/T]GAGACCAAAATGGCT | 5607 |
rs370456542 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742001 | CCAGGTTCATGCCAT[C/T]CTCCTGCCTCAGCCT | 5607 |
rs370479170 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800321 | GTGGGGTTTTTTTTT[-/T]AGCATGAATGTATTA | 5607 |
rs370480141 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598127 | GGAGAATCATTTGAA[C/T]TTGAGATGTGGAGTT | 5607 |
rs370514365 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544242 | TTTTACTTAGAAAAA[A/T]ATGCTAACCATGACA | 5607 |
rs370516951 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553845 | GTGAACCCGGGAAGC[A/G]GAGCTTGCAGTGAGC | 5607 |
rs370535680 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589398 | TTATTAAACTGGGTT[A/T]ACTAATGCACATGGT | 5607 |
rs370570113 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784093 | ACATAAAACATTTTA[A/G]ACACTTAAGTTAGAG | 5607 |
rs370580846 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584203 | TATAGTAATTCCTGA[C/G]CCGATAACTTTAGGA | 5607 |
rs370611701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651784 | ACTCAGATTGATTTC[A/G]TATCTTGGCTATTGT | 5607 |
rs370624734 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613730 | CTTCAGCTCCCTAGG[A/G]AAGCTTCTCCATACT | 5607 |
rs370628330 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661463 | GCTTTGTCAAGTCAT[C/T]GTTGTGAAACCCAGC | 5607 |
rs370637616 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700101 | TTCCTTTTTTGGAAG[A/G]GATAAGGGATATACC | 5607 |
rs370645634 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726033 | TTCTTTCACCCCATC[A/T]TGTGATGTTTTTGTT | 5607 |
rs370647673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747124 | CTGAGGCCTCAGGCC[C/T]GGACACTGTCCTCTG | 5607 |
rs370654512 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703911 | AAAAAAATCACCTCA[C/T]TCCAGTATAGTCTTA | 5607 |
rs370699369 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559157 | ATTATGTTTTCATTT[A/C]TTTTCTCTTACCTGG | 5607 |
rs370701285 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541807 | GGTTGTGGTGAGTAG[A/G]GGTCGCGCCGTTGCA | 5607 |
rs370716132 | snp | A/C/G | 3.55948e-05 | 0.00421855 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642533 | GGTGGCATTCAAGCT[A/C/G]GGTCTAAAAGATAGA | 5607 |
rs370723628 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698922 | ATCTTCACACAACCC[A/C]AGGAGGTATACGTAT | 5607 |
rs370729818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664227 | GGCCAGGTGTGGTGG[C/T]TTACGCCTGTAATCC | 5607 |
rs370755583 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573204 | CCCTCACTCAAGATG[C/G]AGTTGCTCTGGTTCA | 5607 |
rs370760935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723205 | TTTGTCAATAAATAA[C/T]TTCTTTTTGTTAAAA | 5607 |
rs370774042 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739390 | ACAGTCAAGCCAGTA[A/C]GACACATGTTAATTC | 5607 |
rs370777968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762048 | CCTTTAGACCAGCCT[A/G]AGCAGGAGACTTCCC | 5607 |
rs370803546 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549985 | ATTTGCCACATGTTA[A/G]CAATAAAGAAGATGG | 5607 |
rs370816702 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636849 | TTGAGTTAATGTTAA[C/T]GTAAGAGATTAACAT | 5607 |
rs370818316 | in-del | -/TGT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545869 | TAAGCGCTCCATTAG[-/TGT]TGTTATTATTGATGG | 5607 |
rs370840134 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712954 | GAAGTTCATGACAAC[G/T]TCTCATTAAAGAACC | 5607 |
rs370844577 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754856 | TTACCCTGTAGCCAA[A/G]GGATATGCTTGGAAG | 5607 |
rs370853706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769780 | AGACAGGAGGGACTT[C/T]GGGGCCTTGGGCAGA | 5607 |
rs370858751 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726215 | ACACATACACACAAG[C/T]ATATGTGCAAATGAG | 5607 |
rs370860060 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787143 | ATAGGCAGGCAGGGC[A/G]GACAACAGGACTGAT | 5607 |
rs370861365 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592117 | GAGTGAAACTATGTC[A/T]CAAAAAAAAAAAAAA | 5607 |
rs370865640 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600350 | ATGTGCAGTGCTCTT[C/T]GGCATTGGTTATATG | 5607 |
rs370878726 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714284 | TTGAAGAAGTAAGCC[C/T]TTTGAAATAGCATCT | 5607 |
rs370904660 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797863 | AATTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 5607 |
rs370924120 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544913 | CCTTCTCTTTGTATC[C/T]GGAGTTCTCCACACA | 5607 |
rs370941072 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684121 | CTAGAAATTGCATAG[C/G]AGTTCCCTTGCGTCT | 5607 |
rs370944412 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601336 | TCTTAAAAAATGCTA[A/G]CCATAAAAAATAGTT | 5607 |
rs370953340 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580961 | GAAGTATTCATTATC[A/G]TGGGGATTGCAGGCT | 5607 |
rs370964905 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706554 | AGGAGCCGGGTGTTA[-/A]CAGCAGGAGGAAGAG | 5607 |
rs370972242 | snp | A/C/T | 7.54822e-05 | 0.00614298 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806848 | GCCAGAAGAGCTTTG[A/C/T]TGGGCCCTGGCTTCC | 5607 |
rs370981362 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550668 | ATGAGTCATGCTACG[A/G]TGAGATAGTCAGTAG | 5607 |
rs371000189 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668611 | ACAGCTCCAGTCATA[C/G]CCATCATTACCCACA | 5607 |
rs371006879 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648423 | CATTCCTTTTTATTG[C/T]TGAATAACATTTCGT | 5607 |
rs371012740 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685517 | AATAGTTTCACAAAT[C/T]GTGGATAAATAAAAA | 5607 |
rs371027853 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705225 | ATATAAATGTTCACT[A/G]TTCATCCTTTCTACA | 5607 |
rs371064447 | in-del | A/GAC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774209 | TGTGTGTGTGAGAGA[A/GAC]CATAGGTATTTAGAT | 5607 |
rs371067018 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657668 | CAAAGTTTAACTAAG[A/C]GTGATCATTTTTCTC | 5607 |
rs371074103 | snp | A/G/T | 0.000353591 | 0.0132926 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806758 | CCCCGTGAGGCTGCC[A/G/T]CAGGGCACTGAAAGC | 5607 |
rs371094710 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571633 | TTTTTAAGAAGGTTT[C/T]CCATATACCAGCTCC | 5607 |
rs371096821 | snp | A/G | 3.31345e-05 | 0.00407016 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703299 | GTTTTCCTGAGTAGC[A/G]TCCGTCCACTCACAG | 5607 |
rs371103988 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640957 | TTTCATAATGACCAT[A/G]TGTAATTCATGAAAC | 5607 |
rs371118795 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550119 | TCTTGACTATTCCTT[C/T]CTGCAGTCATTTTTT | 5607 |
rs371189333 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550777 | TTCTTTTTCTTTTTT[C/T]TTTTTTTTTTTTGCC | 5607 |
rs371222435 | snp | A/T | 3.3018e-05 | 0.00406299 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580711 | GTGTCTGTTCCAGTA[A/T]TCATACATTACTGAG | 5607 |
rs371223524 | snp | C/T | 8.53002e-05 | 0.00653015 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664561 | TTTTAAAAACCATAA[C/T]TGATAATTGTACTGT | 5607 |
rs371231288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806442 | GCCAGCACTCCACAC[A/G]CTTGGTGCTGACTAC | 5607 |
rs371246955 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701260 | ACAGACATGAATAGC[A/G]ATGTATGAGGAAGTT | 5607 |
rs371247168 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700781 | AAAATTTTTGCTCAA[A/C]CACTGCATCACAGCA | 5607 |
rs371260818 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721215 | TATCTGTAATGCTGT[C/G]TTTTCTCCCTTATTA | 5607 |
rs371266060 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747680 | CCCTGGAAACAGGCA[A/G]AAGGAACTTTGGAAA | 5607 |
rs371287123 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800270 | GAACATGTTTTATTA[G/T]GTAAAATTAATGCAA | 5607 |
rs371295667 | in-del | -/TTTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676138 | GTGTGTGGATGAGTG[-/TTTG]ATTCACCAAGCCCCG | 5607 |
rs371322753 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711449 | AGCCTCAGTTTCCTC[C/G]TCTTTAGATGGGAGA | 5607 |
rs371324847 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588162 | GCCCTTCACATATGG[C/G]TGCTCTGTGTACTCC | 5607 |
rs371329904 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788725 | ATCATGCTTAATTCT[A/G]GCTCTTGGGGGGCTG | 5607 |
rs371358126 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727963 | AAGATTGTTCATTAC[A/T]GCTGTTTGCCACTGT | 5607 |
rs371374326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785681 | ATGGAGCCATGACCT[C/T]GCTCATCCTATGACC | 5607 |
rs371376180 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686478 | TGGGGGTGGTGGCAG[A/G]CGCCTGTAATCCTGG | 5607 |
rs371386235 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804589 | CCCTTCTGGAATGTG[A/G]AGGAACGCCTCTACG | 5607 |
rs371388405 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734476 | GAGTAGAAAGCATAT[A/G]TTCTTAAAACTATTT | 5607 |
rs371391649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752309 | TGACCTCAAGTGATC[C/T]GCCTACCTTGGCCTC | 5607 |
rs371403834 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638509 | CCATGTCTTTGCTAT[C/T]GCGAATAGTGCTGCA | 5607 |
rs371416747 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763379 | TACTCACACTCTAAA[C/T]GAGACTCATTCTCGG | 5607 |
rs371430781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725664 | TATTAGCTTTTTTAG[A/G]TGTGAGACTCTCCTC | 5607 |
rs371469904 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674430 | TTAATCACATCCAGC[A/G]CTATAGTAGATTATA | 5607 |
rs371491036 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557868 | TAAACTATTGTATAT[A/G]TAAAAATATAAAGGG | 5607 |
rs371493858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705365 | CAAGGGCTGGGGCAT[A/G]AGGGGAAGGACAGAG | 5607 |
rs371497522 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577022 | CTCACTGCAAGCTCC[A/G]CTTCCCGGGTTCACG | 5607 |
rs371509884 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604534 | TCACTAATTAGCTAC[A/G]TAACCTTTGGCAAGT | 5607 |
rs371513682 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612357 | CTAATTTTTGAGGGA[A/G]AATGTTCTAACACAG | 5607 |
rs371563615 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545434 | TTTGGGTTTAATTGC[A/G]AGCTGTCCCACTGAC | 5607 |
rs371570300 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586464 | AGAAACATTCTACAT[A/T]CAGTGTTCTGCTTGG | 5607 |
rs371588259 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768176 | TGGAAACAAAGCCTT[A/C]ATAAGAGTTCTAGTT | 5607 |
rs371619860 | snp | C/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719727 | AAATCTATCTACTCA[C/T]CTGTTGCAACATCTC | 5607 |
rs371645345 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694267 | GAAAAAAAATTAAAC[A/G/T]GGAAACTTATCTAGT | 5607 |
rs371666709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590840 | AATAACCAGAGCAGC[A/G]ACCACCATTTATGGA | 5607 |
rs371668871 | in-del | -/CA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727206 | CTCTGGCTCAAAAAA[-/CA]GTTTATATCTTTTTG | 5607 |
rs371686872 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554875 | AAATGAGTAATTTGC[A/G]TTTTTGGATTATTTG | 5607 |
rs371694589 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687109 | GCTGCAGTAAAATTG[-/A]TTTTTTTAATGAGAT | 5607 |
rs371705382 | in-del | -/A/AA | 0.490007 | 0.0699769 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699970 | GGATCTTGCCAATGT[-/A/AA]AAAAAAAAAAAAAAA | 5607 |
rs371708782 | in-del | -/TGAAGGGAGAATGTGC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622170 | AAAAAAAAAAGAAGA[-/TGAAGGGAGAATGTGC]TGAAGGGAGAATGTG | 5607 |
rs371724096 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556268 | TCTGGTCTTCTTATT[A/C/T]TCTCTTCTTTTTTCC | 5607 |
rs371743080 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707145 | TGGCCTCGATCTCCT[C/G]ACCTTGTGATCTGCC | 5607 |
rs371756871 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649085 | TAAAATTGTGGGCTT[A/G]TAGTGTGACATGGTA | 5607 |
rs371774161 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806601 | AGTACAATGAGCGCG[C/G]GAGTCCGAGGACTGC | 5607 |
rs371808506 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543263 | CACTCCCCTTGTCAC[C/G]TCTTGGAGCCCCCTC | 5607 |
rs371832604 | in-del | -/CT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725833 | ATCAGTGTGCACACT[-/CT]GATTGGCCAGAAACA | 5607 |
rs371839540 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789183 | CATATAATATAAAGA[G/T]CAACCTTATTCTTAA | 5607 |
rs371856653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697833 | TCTGTAATCGAAAGC[A/G]TAAAATATAGAAAAG | 5607 |
rs371859396 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551467 | CCTCCCAAGTAACTG[A/G]GACTACACGCATGCA | 5607 |
rs371873195 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670209 | ACCAGCTGTGTGATT[C/G]CACTTATATGACATT | 5607 |
rs371877631 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597094 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 5607 |
rs371889366 | snp | A/G | 3.37467e-05 | 0.00410758 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592967 | AAAAAATACTAGCCA[A/G]TGGCCAGGTAGGTAT | 5607 |
rs371917873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674301 | AGGCTGTTTAATCAG[A/G]TGGGTCTGGAAGGAG | 5607 |
rs371942173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742621 | GAGAAAAGACTGATA[C/T]GGCAAATGTCTAAAA | 5607 |
rs371979753 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595977 | TAAAGTTATTTTTTC[C/T]TTTTTTTTTTTTGTT | 5607 |
rs372016427 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590046 | GTGTATTTTTTCCAT[A/C]TATGTTTCAGCTTTC | 5607 |
rs372024244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714753 | GTACTCCCAAATTCG[A/G]AATTTTTTGAGCACT | 5607 |
rs372037776 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632665 | TCCAATATGCCTTTT[-/T]AGCTATCCACAGTGA | 5607 |
rs372040993 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681536 | ATCTTTTAAAATGAA[A/G]AAAGGAGTATTGGAT | 5607 |
rs372042789 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756497 | TCAAGCTAATATATC[C/T]AACCCCACACACAGT | 5607 |
rs372049315 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792240 | CTGGACCTTCTGGCT[C/T]TAGGCAAAGTCCCCT | 5607 |
rs372053169 | snp | G/T | 0.000247584 | 0.0111234 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748607 | TGTTGATGAGGTGAG[G/T]CATCGTCTTATGTGC | 5607 |
rs372073614 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609474 | AGGTCTATAGATTCT[A/G]TAGACCTATTCTATA | 5607 |
rs372075824 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582441 | TTCACAAGGAGTAGT[A/G]TTTTACAAACTGAAA | 5607 |
rs372080402 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574641 | TGGGAGGCCGAGGTG[G/T]GCGAATCACGAAGTA | 5607 |
rs372085295 | snp | A/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672096 | GTTCCAAGTCTTTGC[A/T]ATTGTGAATAGTGCT | 5607 |
rs372086688 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547057 | GTCACAGAGCGAGAC[C/G]CTATCTCAAAAAAGA | 5607 |
rs372088915 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617847 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 5607 |
rs372089160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644351 | GTGAGCCAAGATCGC[A/G]CCACTACACTCCAGC | 5607 |
rs372095336 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546362 | GCTAAAGCCACCCAG[C/T]TAATTTTTGGCAGAA | 5607 |
rs372096977 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801162 | GTTATCACAGCCAAG[C/T]GGGCTGGAATCCTAA | 5607 |
rs372184412 | snp | A/G | 4.94858e-05 | 0.00497398 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703413 | CTTTTATGGAGGTAC[A/G]TTGTTTGCACATAGA | 5607 |
rs372202951 | in-del | -/C | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547455 | TCGGTTTTCTTTTTT[-/C]TTTTTTTTTTTTTTT | 5607 |
rs372224789 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696413 | CATTTGCAGCAGAAA[A/G]TATATGGCTCATAAC | 5607 |
rs372233315 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638860 | AGGATTGTTGGCCTC[A/G]TGTATATCTTCTTTT | 5607 |
rs372245393 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778119 | TTGGGGGCTAATAAA[-/A]CACCAAACTGCTCTA | 5607 |
rs372253412 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612181 | TGGTCTTTATAAGGA[A/G]GTTAGTTTCCCTCCT | 5607 |
rs372261264 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742156 | TCAGCCTCCCAAAGT[A/G]CTGGGATTGCAGGCG | 5607 |
rs372293991 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546225 | AGAACCAAGAGACAC[A/C/G]TCAGCATCTCTGGCT | 5607 |
rs372306946 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649572 | ATTTGTTCCAGTACC[A/G]TTTGTTAAAGACTGT | 5607 |
rs372340354 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794709 | AAGTTTTGATGTTTT[A/G]ATGTCCAGTGTCTAG | 5607 |
rs372353339 | snp | A/G | 8.23771e-05 | 0.0064173 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586796 | TATAGGTTAATTAGA[A/G]CTGTGTCCTCAGAAC | 5607 |
rs372376117 | snp | G/T | 3.34448e-05 | 0.00408917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769564 | GAAAGAGAAGGAACT[G/T]TTGTGACTTTTGGTG | 5607 |
rs372381811 | snp | G/T | 1.65542e-05 | 0.00287695 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703458 | TCTGTACTAATATAT[G/T]CAATCAGGAAAAGTG | 5607 |
rs372392655 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764427 | CGTTTGTGAACTCGC[A/G]TCTGCCAGCCAAACT | 5607 |
rs372393331 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756810 | TCTGTGTCTGACTTA[C/T]TTCACTTAGCATATT | 5607 |
rs372395702 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692599 | TCTCTGCAACAACCC[C/G]TTTATATTTTCATTC | 5607 |
rs372429281 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718062 | AGTTAAGTTTTGATG[A/G]ATGGGTTAGATTTGG | 5607 |
rs372441406 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624156 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 5607 |
rs372445279 | in-del | -/T | 0.0505692 | 0.150756 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732672 | CATCTTTAAATTTCA[-/T]TTTTTTTTTCAAAAA | 5607 |
rs372447327 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774955 | AAATACTGGAAGTTA[C/T]AGATTCACTATTTGG | 5607 |
rs372448371 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747285 | ATTACTAGTTTCCCT[A/G]TATTTTACCGGCTGG | 5607 |
rs372450054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577867 | TTAGCCGGGCCAGTG[A/G]TGGGTGCCTGTAATC | 5607 |
rs372451397 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598631 | CCCTTCTCTTTTCCC[-/C]TGTAGTGGATGTAAG | 5607 |
rs372451823 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575367 | AACCCATGGAGGTGG[C/T]GGGGCGGGGGAGGGC | 5607 |
rs372460891 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716670 | TTCTCTTAGCAGTGA[A/G]GAAGCTGGTCTCCAG | 5607 |
rs372470513 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612073 | TTTATCTTTGGTTTT[-/C]TTTTTTTTTTTTTTT | 5607 |
rs372486139 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635292 | CCATTCTTCTGCCTC[A/G]GCCTCCCGAGTAGCT | 5607 |
rs372487682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781215 | AGCAAAGTTGTTTTC[C/T]TGTGAGTACACACCG | 5607 |
rs372495824 | snp | A/G | 3.30087e-05 | 0.00406242 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563338 | TGAGGAAATGAAGGC[A/G]ATGCTGTCATATGTA | 5607 |
rs372503235 | snp | C/T | 0.000350984 | 0.0132427 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806809 | GAACAACCCACCCGT[C/T]GCCCTTCTCCGTATG | 5607 |
rs372509154 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634625 | TCTTAGGTGCATTTA[C/T]GTTTGTTATGTCCTC | 5607 |
rs372547110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728867 | TGCTTATAAAGATGG[C/T]AGAGAGAATGAGCCC | 5607 |
rs372555299 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543431 | CGCGGTGGACTGGAC[A/G]GTGCACTCCGGGCCG | 5607 |
rs372557141 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573404 | ACAGTTGGGTAGAGG[G/T]TGGGGCGGGAGTTGC | 5607 |
rs372567587 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735856 | GGCTTTCACGTGGCA[A/G]CTTTGCTATTATCTC | 5607 |
rs372569900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696355 | GCTTATATATTATGC[A/G]TGGCCCCTTTAGCAC | 5607 |
rs372605328 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690071 | GTGTATTTTATATGT[-/G]GTCCAAGACAGTTCT | 5607 |
rs372606956 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557029 | CATAACCATAAAAAA[-/A]TCCTGTGTGTTTGCA | 5607 |
rs372616447 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690226 | TTTGAAAAATAAGAC[C/T]AAACTATGTAGAATC | 5607 |
rs372621062 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562288 | TATTTGGAAATAGCC[A/G]TAAGTCATTCTTAGA | 5607 |
rs372649869 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614158 | CTTCCCACTCCAGTA[C/G]TTACAGATAGGAATC | 5607 |
rs372659266 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579395 | TTTGAGTAATGGCGA[A/G]TGCTGTATTTCTGTG | 5607 |
rs372665049 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582059 | GGATGTAGATGATTT[-/C]TTTTTTTTTTTTTTT | 5607 |
rs372678932 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553216 | GAAATGATTGCTGAA[C/T]GTGATTGCTTGGAAC | 5607 |
rs372682705 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742824 | GGCTCTTATACACCT[A/T]TGTGGTGTGGGACAT | 5607 |
rs372726733 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722239 | ATGGCGTTATACATT[A/G]AAAATTGAAGCTTTC | 5607 |
rs372743619 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753888 | AAAACATATGTCCGC[A/G]TAAAAACTTATACAT | 5607 |
rs372778032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655856 | ATTAAGCATATGTCC[A/G]TATGCTGGATGGTAT | 5607 |
rs372783559 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677528 | CCAAGTCAAGTCTGC[C/T]GTCTTACATCTTATT | 5607 |
rs372787436 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639216 | GGAGAAAAATTTTGC[A/G]AACTATGCATCTGAC | 5607 |
rs372804935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566951 | TTTGTCATGACAATA[A/G]GTTGTTGTGTGCTGT | 5607 |
rs372822426 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603634 | TCATTTTTGCTCAGG[C/T]TTCAGCTTGTATTAT | 5607 |
rs372841112 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583492 | TTTTAATATGCTATG[G/T]TGTAATTGTTTCTAG | 5607 |
rs372893864 | snp | A/G | 0.000430235 | 0.0146606 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593024 | TAATAACATATTACC[A/G]TCCAGTTTTTGTATC | 5607 |
rs372909954 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694195 | TAAGGGAAGTTATTT[C/G]TTTTCATAAAAATAC | 5607 |
rs372924957 | snp | A/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802710 | CTAGATGCCTGGGGC[A/G/T]GTCACCGTGGGTGGA | 5607 |
rs372942208 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618235 | TTGTGCAAAGTACTT[C/T]GCTTGGCAGTGGGGG | 5607 |
rs372945493 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558150 | GAGTCCTTTACTCAA[A/G]CACCAGACTAGTTGT | 5607 |
rs372946464 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582481 | AATTTCTCTATTGAC[A/G]TTATAGCTCTGCCAT | 5607 |
rs372947501 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582751 | GCTTGAGCCCAAGAG[A/G]TTGAGGCTACAGTGA | 5607 |
rs372951744 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680056 | TTTCTGGACATTTTA[C/T]ATAAGCAGAAACATA | 5607 |
rs372957139 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790913 | GTCCTGTGAGGTTGA[A/T]GCTGTTCTCCATATT | 5607 |
rs372965288 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757393 | CCTTTATGTTGCTCA[A/G]AAACCCAACCTATAA | 5607 |
rs372969258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654605 | TGTTCTGTTGTTGCT[C/T]TCTTTTATATCAAGT | 5607 |
rs372971869 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744500 | TCTTCCAGACAAGAG[C/T]TGCAGGGCAAGCCAT | 5607 |
rs372973858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776655 | GGGGGTTCAGGTTGG[C/T]TTTGCTATTCAATTT | 5607 |
rs373011561 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607097 | TGGTTTTAAAATTGA[A/C]CTGAGAGCTAGAATG | 5607 |
rs373083413 | snp | C/T | 1.6596e-05 | 0.00288058 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67630892 | TCTTCCCATAGAGCA[C/T]ATCATGTCCCGAGTG | 5607 |
rs373100488 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676086 | ATAGTATCCATTAGG[G/T]TAAGCTTCTATCCAA | 5607 |
rs373104308 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718630 | TTAGCCAGGCGTGGT[A/G]GTATGCACCTGTAAT | 5607 |
rs373106048 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746434 | TAGGAATGTAGGGGT[C/G/T]GGGGGAGTATCAGTG | 5607 |
rs373127117 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610719 | CTCCTCCAATTCAAC[A/G/T]TTAGTGTACAAATCA | 5607 |
rs373138718 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673883 | AAACAGAGTCTCACT[C/T]TGCCGCCCAGGCTGG | 5607 |
rs373146659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695087 | ACACAGGAATGGGAA[C/T]ATCACACTCTGGGGA | 5607 |
rs373161731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768516 | TGATATATTGCTCAT[C/T]CAAATGGCCAAAGCA | 5607 |
rs373165792 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778611 | GTCTTAGAGAAGTCA[C/T]GAGGAAAGATGGAAA | 5607 |
rs373166975 | snp | C/T | 1.67944e-05 | 0.00289775 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769708 | TCAATGTAAATGATA[C/T]ATGCCATTAACTCGG | 5607 |
rs373183429 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706776 | ATAGTGTAAGGCCCC[-/T]GGCATGTTTTATATA | 5607 |
rs373192450 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584262 | CTGTTTACATCTCCA[A/G]TTATAAAAGTTTGAG | 5607 |
rs373235724 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709534 | AAATGAGTTTGTTAT[A/G]TAATAAGGGCTTTAC | 5607 |
rs373245388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735680 | CAAGAGGGTTTCACA[C/G]AGTAGATAGCTGACG | 5607 |
rs373279612 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713764 | AGTGGCATGGATCAC[C/G]CAGCCCAGTACCCTT | 5607 |
rs373288102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772644 | ATAGCCATTGGTAGA[A/G]ATTATAGCAAAAATA | 5607 |
rs373300582 | in-del | -/GG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565364 | CCTCCTGAGTAGCTG[-/GG]ATTACAGGCACCCAC | 5607 |
rs373307238 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748508 | GATTTTTTCTTTCCA[C/T]TCCACTGTAAAGATA | 5607 |
rs373331010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643547 | CGCCTCCTGGGTTCA[C/T]GCCATTCTTCTGCCT | 5607 |
rs373348038 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800256 | AAACTTTAACAGTGG[A/G]ACATGTTTTATTATG | 5607 |
rs373381176 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660597 | CAAAAGCAACAGAAT[C/G]AGAAACAGAGAGTAG | 5607 |
rs373443851 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553912 | GCGACAGAGCGAGAC[A/T]CCATCTCAAAAAAAA | 5607 |
rs373520077 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623537 | CACTACTGCTCTTTA[A/C]GTCTGTTTTGGCAGC | 5607 |
rs373529511 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798252 | TCCCTCTGGGCATCT[-/G]CGTGGCCCAAAACTG | 5607 |
rs373538265 | snp | C/T | 3.31356e-05 | 0.00407022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703302 | TTCCTGAGTAGCATC[C/T]GTCCACTCACAGGCT | 5607 |
rs373553768 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553386 | TTTCTTTTGCCCCAT[C/T]AATGGCAGCAGCTCT | 5607 |
rs373580596 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751164 | AACAAAGCCAGAGTT[A/G]GCTACCAGATGTCCA | 5607 |
rs373582585 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643899 | TATAATGCATAACTT[A/T]TGCTTTTTTCTTCAG | 5607 |
rs373587720 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769722 | ACATGCCATTAACTC[A/G]GCAGCTCCGTGAGAC | 5607 |
rs373597404 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586883 | CTCAACACAGCAGCC[C/T]AGCAGTCTCAGATTC | 5607 |
rs373602493 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698216 | TTTTCTTGAGATGAA[A/G]TCTCACCCTGTCCCC | 5607 |
rs373638598 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623814 | GTTGGTCAGGCTGGT[C/T]TCGAACTCCCAACCT | 5607 |
rs373675475 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604199 | CTGTGCTCTATATTA[C/T]GAGAGTGACTTAGGC | 5607 |
rs373696975 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800228 | TTCTCCGGGGATTAG[-/A]TTGGTAGCTTTAAAA | 5607 |
rs373699498 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653400 | AAGCCGTTCTCCTGC[C/T]TCAGCCTCCAGAGTA | 5607 |
rs373704854 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756049 | AAAGCCAGCATCTCT[A/C]CCCCACACTAGGGCA | 5607 |
rs373705091 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616629 | AGCTAATAACAAATA[A/C]ATTTGTAACTTTTAT | 5607 |
rs373707183 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782952 | GCAGTGCTGCATCAT[A/C]TGGAAAGTGGGTTAA | 5607 |
rs373717251 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774063 | CCCATAAATGTATAT[A/G]GATGTATATGTTGGT | 5607 |
rs373734184 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553774 | AAAAATTAGCCGGGC[A/G]CGGTGGCGGGCGCCT | 5607 |
rs373813037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724599 | CATGCAGCCATATCT[A/G]CTAAGAAACCATTTT | 5607 |
rs373854775 | snp | A/C | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547075 | ATCTCAAAAAAGAAG[A/C]AAACACACACACACA | 5607 |
rs373865192 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710821 | CTTCTGAAGATTTTT[G/T]GGGCTCTATTATTTT | 5607 |
rs373906395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806110 | CAGCACATTCCTCCC[C/T]CTCCCCACTTCCCCT | 5607 |
rs373911910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628458 | GCTCTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 5607 |
rs373917264 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745075 | AAGAGGTTCATCTAT[C/T]AAAATGCAACTAGTT | 5607 |
rs373918348 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593576 | GTAGAGTGCTTTTAA[A/T]CATACACTGGTAAAT | 5607 |
rs373986190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792615 | CTCCAGACCCTAAAA[C/T]ATAAAACTTCCCACT | 5607 |
rs373998284 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769053 | TAGACTGGCAAATAG[A/G]CTGAAATTCCTTTTC | 5607 |
rs374014414 | snp | C/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541656 | CCAACATAGTGAAAC[C/G]CAGTCTCTACTGAAA | 5607 |
rs374017078 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708160 | ATCTCTAAAAAAACA[A/G/T]TTTTTTTTTTCATTT | 5607 |
rs374023142 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544317 | CGGTAAAAGTAAGGG[A/G]AAATGTGCATCTTAG | 5607 |
rs374024605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742053 | GTGTCTGCCACCACA[A/C]CCGGCTAATTTTTTG | 5607 |
rs374025700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785092 | TAGCTGAGACTACAC[A/G]TGAACAACACTATGG | 5607 |
rs374052210 | snp | A/G | 3.56754e-05 | 0.00422332 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646314 | GGTAATTTTTTCATA[A/G]TTTTTATTTGTAAAG | 5607 |
rs374085218 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715656 | AATTTAAAAAAAAGC[A/G]AAGTCTTGATATGAA | 5607 |
rs374139864 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563211 | ACATTGTAATAAACC[A/G]TTTATATTATGTTCC | 5607 |
rs374140981 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559747 | TGCTCCAGGCAACTA[C/G]AGAAGCCTGGAATTC | 5607 |
rs374142594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783540 | GACTTCCTTTTGCCT[A/G]TCACCCTTCACCCTG | 5607 |
rs374165114 | snp | C/T | 0.000149126 | 0.00863371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563360 | TCATATGTAAGTATA[C/T]GACAAATGAAGACTA | 5607 |
rs374194781 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702034 | CTGAGGGCAATAATA[C/T]CTACTTTTGCAAAAT | 5607 |
rs374220165 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546508 | CCCTGGGCAAGTCAG[C/T]CGGTCTCTCTGGGCC | 5607 |
rs374228851 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634449 | TATTGTATAATGTCA[A/C]TTAGATCAAGTTGGC | 5607 |
rs374236488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663638 | AGGGATTTGGGAGGC[C/T]GAGGCAGGAGGATCC | 5607 |
rs374243793 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679006 | TACAAGGAAATTACC[G/T]TTTGGGTCCCTATAC | 5607 |
rs374251089 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557765 | AGCCATGACAATCTT[A/G]TTAAGAATAGTTGGG | 5607 |
rs374254461 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710567 | GGAGTGCAGTGGCAC[A/G]GTCTTAACTCATTGC | 5607 |
rs374262486 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549651 | TTAGGTGATTTTTTT[-/T]CCCAGAGATTCAGAC | 5607 |
rs374269296 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728900 | TTTAAGCAAATTCTC[C/T]TGGTACCAATGTGGA | 5607 |
rs374299556 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684709 | TATTATAAAAACTAT[A/G]TATGTCCAAGGAATT | 5607 |
rs374304568 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647307 | AGTAGAATGTCAAAA[A/T]TTAAAAATCTTACAG | 5607 |
rs374305355 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733965 | GGTGGCATTTGCTTC[A/T]GAACCTCCTGCTATT | 5607 |
rs374342399 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612122 | GTGAGTTAGTTTATG[A/T]GTGTATTTAAATCAT | 5607 |
rs374345945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634156 | TTGAGCTCAGGAGTA[C/T]GAGACCAGCCTGGGA | 5607 |
rs374352802 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595284 | TGATTCAGCATTGAT[A/C]TAGTGTCAACAGTTC | 5607 |
rs374367631 | snp | A/C | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671997 | GGACATGAACTCATC[A/C]TTTTGTATGGCTGCA | 5607 |
rs374381003 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649793 | GTGTAAGTGCTCCAA[A/C]TTTGTTCTTTTCAAG | 5607 |
rs374385125 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607908 | TACAAACAACTTTTC[A/G]GTCAATTGAGTCTGG | 5607 |
rs374394177 | snp | A/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670465 | GAGTGAATTTTACTG[A/T]GTATAAATTATGCCT | 5607 |
rs374396630 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708079 | CCAGCACTTTGAGAG[A/G]CTGAGGCAGGAGGAT | 5607 |
rs374401492 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585114 | AATTAATTCGTCCCC[A/G]AACAATCAATCAAAA | 5607 |
rs374449295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631566 | TGACTCCCTCGGCAT[A/G]CTGAAATACCCAAGC | 5607 |
rs374460533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691641 | GAAGCAGATGCTGCT[C/T]TATACCATCAAAAGT | 5607 |
rs374463383 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671940 | TCCTCATGATAGTTT[A/G]CTGAGAATGATGATT | 5607 |
rs374480369 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773889 | TTCTAGAGATGGAGA[C/T]CCATTTACCTTGTGC | 5607 |
rs374490895 | snp | A/T | 2.43099e-05 | 0.00348631 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646332 | TTTATTTGTAAAGCA[A/T]GCCTATGGTATTGAC | 5607 |
rs374491044 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715236 | TTTTTTTGGGCGGGG[-/A]GGGGGGGGGTCTAAA | 5607 |
rs374546618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562759 | CTCATAACAAACCTG[C/T]GACATGAACATCATT | 5607 |
rs374592683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668749 | AGGGTAATGAGAATA[G/T]AATTTAGATTAAGAA | 5607 |
rs374594158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705294 | TGCTGTATAGGCAAT[A/G]GGGATAGAGTAAGGA | 5607 |
rs374599028 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755189 | TCACCATGTTGGCCA[A/G]GCTGGTCTCAAACTC | 5607 |
rs374604228 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734357 | GCTTGGAAACGTGCT[A/G]TTTTAATGTGTTTTG | 5607 |
rs374615548 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666708 | GTACTTACTTTTTCA[C/G]TTGGTGCTGGCCAGC | 5607 |
rs374632221 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645756 | TGGGTTCTCGCTATG[A/G]TGCTTAGACTGGCCA | 5607 |
rs374634594 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683507 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 5607 |
rs374638888 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648518 | TTTATGCATAATTAT[G/T]AATAATGCTACTCTA | 5607 |
rs374641215 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788242 | CTGGGGCCCCCAGGC[C/G]TTCTCCCCTTTTTTT | 5607 |
rs374645558 | snp | A/G | 9.88093e-05 | 0.00702815 | missense | MAP2K5 | GRCh38.p7 | 15:67806673 | ATCGTGCAGTTCAAT[A/G]ATGGAAATGCCGCCG | 5607 |
rs374650144 | in-del | -/A/AA/AAA | 0.448708 | 0.151707 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585076 | ATCTGAGAGAGGAGC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 5607 |
rs374657490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702686 | GGGTATTTGCTATAC[A/G]TCTTGAGTGGAGGAC | 5607 |
rs374673286 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549467 | GTGTCGAACTCCTAC[C/G]ATGATGAGTGCGAGG | 5607 |
rs374677476 | snp | G/T | 3.29761e-05 | 0.00406041 | synonymous-codon, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703399 | GAGCTTAGGAATCTC[G/T]TTTATGGAGGTACGT | 5607 |
rs374689318 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623612 | AGCAAAACTCCGTCT[-/A]AAAAAAAAAAAAAAG | 5607 |
rs374700043 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567490 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5607 |
rs374724401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582630 | TTTGAGACCAGCTTG[A/G]GCAACATGTCAAAAC | 5607 |
rs374726311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637329 | AGATGGTATTTAGTT[A/G]CTTTTGAATAATTTG | 5607 |
rs374733204 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575982 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 5607 |
rs374743527 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675042 | GACATTTAAAAAAAA[A/G]AGAAAGAAAGCTAGA | 5607 |
rs374751567 | snp | C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548038 | TTTCTCCCTTTTCCT[C/T]GTATCAGGTGAGGAG | 5607 |
rs374764422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583162 | AAGTAACTTCAGAGT[C/T]ACACAGCTTATAAGT | 5607 |
rs374767723 | snp | C/T | 5.06462e-05 | 0.00503195 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600644 | TGACATTTCCATCCA[C/T]AGCATGACACCCTTT | 5607 |
rs374821397 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738465 | AGGCAGCAAATGACA[C/T]ACCCGACAAGTGACA | 5607 |
rs374837331 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630462 | AGCAAAAAAAATGGG[-/A]AAAAAAAAAGCAAAA | 5607 |
rs374852044 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723131 | GTTTGTTTTCTCTTT[A/G]TCATTTATGATTCTA | 5607 |
rs374854599 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697944 | ATGTGCTTGTAGGAG[A/G]CTTGAAAAGTCATCT | 5607 |
rs374861295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680210 | TATATCACATTTTGT[C/T]TGCTTATTTACTAGT | 5607 |
rs374865831 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642311 | TAGGCACTACTGTGA[A/G]TTAGACCCTGTGTGG | 5607 |
rs374875247 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680582 | TTTACCTAAAACCAC[C/T]TACTATTATCCTTAG | 5607 |
rs374876444 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606655 | ATTAGGTTGTGTTTT[A/G]CACTTGTGATTTGAC | 5607 |
rs374904015 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545535 | CAAAGACTTGGAAAG[A/T]TTATGTGAGATTGTG | 5607 |
rs374917116 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654677 | TTTACTCTGTGTTTT[A/T]GAGTTATATTCTTAA | 5607 |
rs374923947 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582115 | CCACCAGGCTGGAGT[G/T]CAGTGGTGCAATCTC | 5607 |
rs374941743 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608551 | TGGGGGGCTGAGGAA[A/G]AACTGATGGCTTTTA | 5607 |
rs374963326 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598163 | TGAGCCAAGTTCACA[A/C]CACTATACTTCAGCC | 5607 |
rs374981620 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729062 | TTCATAGACTTTTTT[A/G]TTTAAATGTAATCTT | 5607 |
rs374984402 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748912 | ACTGGAAATTAAAAT[C/G]ATATCATTTTTTTCT | 5607 |
rs374985400 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768184 | AAGCCTTAATAAGAG[C/T]TCTAGTTAATTTTCT | 5607 |
rs374990558 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785035 | GCCTCAATCTCCCAG[A/G]CTCAGGTGATCCTCC | 5607 |
rs375008060 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611093 | ATACTGATTCTATTA[C/T]GACGGTTAACTGTAG | 5607 |
rs375029691 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655045 | ACTCCAGACTGGGTG[A/G]CAGAGTGAGACTCCA | 5607 |
rs375035335 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554101 | CTGGCTCTGTCACCC[A/G]GGCTGGAGAGTGCAG | 5607 |
rs375041707 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585992 | TGCTGTGTTCCACTT[A/G]TTGAAATGTCAAATA | 5607 |
rs375064916 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677924 | TGAGACTCCAGGCAA[C/T]AACTGCCATTGAGGA | 5607 |
rs375104745 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658748 | CTTCTTGATTTTCTC[A/C]TGTTTTGTTCTTCTT | 5607 |
rs375115896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696093 | AATCCCTGACTTTTA[A/T]CTGCTGACAGTCTCT | 5607 |
rs375118190 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675324 | CCAGATCATTATACT[G/T]AGTGAAAAAGCCAGT | 5607 |
rs375128013 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623957 | GATCCTCACAACTCT[A/G]TAAGGGAGAGACTGC | 5607 |
rs375128220 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763887 | AATAGAGCTTTGCCA[A/G]TTAGTATGAATCCCA | 5607 |
rs375132524 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783172 | TGCCCAGCATCCTGC[A/C]TGACACCGAGGAGGC | 5607 |
rs375148824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781799 | CAGAAGGCTTCTGAA[C/T]GGCCTGCATCTCTTT | 5607 |
rs375150490 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766420 | CCAGTACTGAGAATT[C/T]AGTGTAACTGCTTCT | 5607 |
rs375151440 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630600 | CTAGTTACTTTGTGC[C/T]ATTGGGCAAACTGTT | 5607 |
rs375161489 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567659 | GTGAGCCACCGCGCC[C/T]GGCCTAAAGTATTTT | 5607 |
rs375161697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586518 | TTGAGGTTCACTACT[A/G]ACCCCTGGGTATATT | 5607 |
rs375188056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706495 | GAGTGAGGGCCAGGA[A/T]GAGCTAGGCCTTTTG | 5607 |
rs375191942 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781233 | TGAGTACACACCGAT[A/C]AATAGATGCAGTTCT | 5607 |
rs375203267 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605196 | AGTAGCTGGGATTAC[A/G]GGCATGTACCACCAT | 5607 |
rs375217000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597332 | TTTAACTTGTGTCTT[C/T]CAGTTGATTGTTTAC | 5607 |
rs375232734 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670085 | ACAGACTGTAATACA[G/T]CCACAGAGTGGAATA | 5607 |
rs375238841 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625066 | CTGCTGTGAAAGAAG[A/G]GGATTAGGTTAAATA | 5607 |
rs375263211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794962 | CTCTGAAACCTCTGA[C/T]GCCCCCGCGGTGGGT | 5607 |
rs375307047 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801550 | CAGTAGGCAGGCAGT[A/G]TGGTGTCTTCCATGG | 5607 |
rs375328431 | snp | A/C | 1.67203e-05 | 0.00289134 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769700 | CCATGCCCTCAATGT[A/C]AATGATACATGCCAT | 5607 |
rs375341218 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645051 | TACTCAGGAGGCTGA[A/G]ACACGAGAATCGCTT | 5607 |
rs375345455 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610029 | TATGAGAAAGATAAC[A/G]TTTGGAAGGGCTAAG | 5607 |
rs375358838 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726034 | TCTTTCACCCCATCT[G/T]GTGATGTTTTTGTTA | 5607 |
rs375362268 | snp | C/T | 0.000115866 | 0.0076105 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67769610 | ATCACAGGATTCGCC[C/T]GTCCTTCCAGTTGGA | 5607 |
rs375365952 | snp | C/T | 4.95741e-05 | 0.00497841 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748566 | TCTTCTTTTCCATTG[C/T]AGCCTCTCCAGCTTC | 5607 |
rs375383624 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791269 | GGAGTTGAGGGATGA[C/G]GCAAAGACTGAAGGA | 5607 |
rs375390707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766699 | ATCAAAACTAACTTT[G/T]TAATTTTATTTGCTT | 5607 |
rs375397433 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603133 | TGTATAGTTAGTGGC[A/G]TTAAGTACATTCACA | 5607 |
rs375398195 | snp | C/T | 3.34403e-05 | 0.00408889 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563392 | TTTTTAAAATCTTAA[C/T]GTGATTGAGGATGCT | 5607 |
rs375400704 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592118 | AGTGAAACTATGTCT[A/C]AAAAAAAAAAAAAAA | 5607 |
rs375407647 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574778 | AGGCTGAGACAGGAG[A/G]ATCATTTGAACCTGG | 5607 |
rs375439419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681542 | TAAAATGAAAAAAGG[A/G]GTATTGGATATTAAA | 5607 |
rs375439795 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681361 | TGAGTACACACACCC[A/G]CACGTACATGTATGC | 5607 |
rs375473688 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615725 | ATTATATTTTTCATT[A/G]GCTGAACCACAGCTG | 5607 |
rs375478487 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771821 | CTTCTTGCTTGTTAG[A/G]AGAGTGCCTTATAAA | 5607 |
rs375522659 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687447 | TGTTATCCTAAAATC[A/G]CATGAACAGTATTTT | 5607 |
rs375532223 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735019 | AATATCCTGATATTT[C/G]AAGCATAAAATCAGA | 5607 |
rs375538274 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569699 | TATTATGTGGCTCTT[A/G]GAAGCAAAGGAAAAG | 5607 |
rs375539526 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552859 | GAGTAGTTTCCAGAG[A/T]GTATATTCTCAACCA | 5607 |
rs375546843 | in-del | -/GTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687390 | AGAAACATCCCTATT[-/GTT]CAGAAAGAAACCCCC | 5607 |
rs375561496 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622975 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 5607 |
rs375597060 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569019 | TCAAAAAAAAAAAAA[A/C]CAAAAAAAAAAAACA | 5607 |
rs375632608 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742180 | GCAGGCGTGAGCCAC[C/T]GCGCCCGGCCAAGAA | 5607 |
rs375644860 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770807 | AGTGTAACATGTTAC[C/T]TCTTAATAAAAATGT | 5607 |
rs375667443 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554350 | AGGTGTGAGCCACCG[C/T]ACCTGGCCTTATAGT | 5607 |
rs375668006 | snp | C/T | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541795 | CCGGGAGGCTGAGGT[C/T]GTGGTGAGTAGAGGT | 5607 |
rs375671982 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785395 | TCACATTGCAGCATG[G/T]CTACTTGTATCATTG | 5607 |
rs375769576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577870 | GCCGGGCCAGTGGTG[A/G]GTGCCTGTAATCCCA | 5607 |
rs375783674 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784764 | AGCTGTCTGGTCACA[A/G]ACCTTTCTGCCTTTC | 5607 |
rs375785004 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733519 | ATTGGGAAAAAAAAA[-/T]ACCATCATCTGGCCA | 5607 |
rs375808848 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565900 | CAGGCGTGAGCCAAG[A/G]TGCCTGGCCAGGTTG | 5607 |
rs375849868 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718278 | GGTTTAGAACTGGAA[A/G]CCCCCAAAGCTAGGT | 5607 |
rs375861660 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574607 | GGTGCTGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 5607 |
rs375868624 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622084 | TGCTACCCAGAGGTG[-/G]CAGTGAGCCGAGATC | 5607 |
rs375871149 | snp | A/C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562700 | TGCTTTACAAGTTAA[A/C/T]CTTGCACTAGGCCTA | 5607 |
rs375875286 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544143 | GCGATTTGCTTGCCT[C/T]GGCCTTCCCAAAGTG | 5607 |
rs375895206 | snp | C/T | 3.29554e-05 | 0.00405914 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727870 | CTTAAGGAGATCTGC[C/T]CTGCATGCAAATCTA | 5607 |
rs375915169 | snp | A/G/T | 5.00541e-05 | 0.00500249 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646406 | GATTCATCATATATC[A/G/T]TTGGATTTTATGGAG | 5607 |
rs375923959 | in-del | -/TATTTAGTGTTCTAGAAGAGGT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613921 | TGTTCTAGAAGAGGT[-/TATTTAGTGTTCTAGAAGAGGT]AATTTAGTAAATTGT | 5607 |
rs375939032 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792055 | TCTGCTCACCTGCAT[C/T]GGTGAGAAGAGAGCC | 5607 |
rs375944410 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674010 | CGTGCCTCCATGCCC[A/G]GCTAATTTTTGTATT | 5607 |
rs375944810 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639234 | CTATGCATCTGACAG[A/G]GTTCTAATATCCCTT | 5607 |
rs375946827 | snp | A/G | 3.30022e-05 | 0.00406202 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748282 | ATGAGTTCAGAAAAA[A/G]ATTCACTTTTCTTTT | 5607 |
rs375950674 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696698 | AGAAAATAAGACAGG[C/T]CAGGCACAGTGGCTC | 5607 |
rs375955821 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799148 | CCCTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 5607 |
rs375969304 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715243 | GGGCGGGGAGGGGGG[G/T]GGTCTAAAATTGTGT | 5607 |
rs376009055 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748381 | AATGCAAACCTTTAA[-/C]CTGCCTGTATTAGAT | 5607 |
rs376010321 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691118 | GAAACAGAATCATCA[A/G]CCACAATGTGTACTT | 5607 |
rs376012588 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718583 | AGCCTGGCCAACATG[A/G]TGAATCCCCGTCTCT | 5607 |
rs376016173 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648989 | TCCAATCTGTTTTAC[A/G]CCACTTTGCATTCAT | 5607 |
rs376041336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686719 | ACTCAGTGATTTACC[A/G]AAGGCTGGGGGTCAG | 5607 |
rs376052237 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541661 | ATAGTGAAACCCAGT[A/C]TCTACTGAAAATACA | 5607 |
rs376067801 | snp | A/G | 0.000193255 | 0.00982804 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806747 | CCAGCAGGGGCCCCC[A/G]TGAGGCTGCCGCAGG | 5607 |
rs376074548 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656406 | CTCTGCTCACTGCAA[A/C]CTTCACCTCCCGGGT | 5607 |
rs376080002 | snp | A/G | 0.000181532 | 0.00952538 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748287 | TTCAGAAAAAAATTC[A/G]CTTTTCTTTTTCCTG | 5607 |
rs376096819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657985 | CTGATAGGAAAAAAT[A/G]TTTGTCAAATACTCT | 5607 |
rs376124890 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741868 | ATCTTACAGAAAGAC[A/T]TACTTCTTGGATTCA | 5607 |
rs376128116 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799273 | GGCATTTGCCCAGGT[A/G]TGCTCGCTATGTGGA | 5607 |
rs376142986 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593431 | CCTGGCCTTCAGGAG[A/C]CCTTAGTTTGCCTAG | 5607 |
rs376144803 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735695 | GAGTAGATAGCTGAC[A/G/T]CTTGAGCCGAGGCTC | 5607 |
rs376162584 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597105 | ACCCGGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG | 5607 |
rs376169765 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723510 | CTTTTACATAATAAA[C/T]GTCCCGCAAGAGAGT | 5607 |
rs376174344 | snp | A/G | 0.000280294 | 0.0118351 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585847 | TGAGCAAATTTGTAA[A/G]TGGCCCTGATGTGTT | 5607 |
rs376207499 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580684 | AAGTACTGTGAATTA[A/G]ACAACCCATAAGTGT | 5607 |
rs376219728 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633671 | ACAACAAGAACTGTA[C/T]TGTATTCACTTTGTA | 5607 |
rs376232455 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627553 | TACATATGCTTTATA[A/T]ATGTAGTTTCCTAGT | 5607 |
rs376288047 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591605 | CAATCTCCTGACCTC[A/G]TGATCCACCTGCACC | 5607 |
rs376311262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604662 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 5607 |
rs376317961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778792 | CGGTTTACTTTGATC[C/T]GGGGCTTACCTGTGC | 5607 |
rs376334842 | snp | A/C/G | 0.000175298 | 0.00936059 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646351 | TATGGTATTGACTTG[A/C/G]AGGTTTATAACTACT | 5607 |
rs376352666 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633146 | CTTGGTTCTCACTGA[C/G]TGTGGCTCTGTTGTA | 5607 |
rs376354549 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671429 | TTAAAACTGAAGATA[A/G]GAGACTAAAGTATAA | 5607 |
rs376368649 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573446 | AAACCATCAGATCTC[A/G]TGAGAATCCACTCAC | 5607 |
rs376396483 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789500 | AGGTGGATCACCTGA[A/G]GTCAGGAGTTCGAGA | 5607 |
rs376422120 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619121 | CCTTGGGCTTTTGAA[-/AAA]CTTGCTGTTTCCTCT | 5607 |
rs376443517 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800926 | AAAAAGTAACACCAC[A/G]GTACAAGGTAACAGA | 5607 |
rs376443801 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755131 | AGGTGTGCACCACCA[C/T]GCCCAGCTAATTTTT | 5607 |
rs376464843 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67550071 | CTGAAGCAACAACTA[C/T]AGCATTTGAATGTAA | 5607 |
rs376470332 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791046 | GAGAGAGCTCCTCAC[A/G]CCATGAATAGTCCAC | 5607 |
rs376484517 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713425 | TAGAGCTGTGTAAAT[A/G]TAAATAAAAGTATTT | 5607 |
rs376499889 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794620 | CTGAGGGTCGGGTAA[C/T]TCTGGAACATCACAG | 5607 |
rs376559323 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674629 | TTTACCTTGGGTGAT[C/T]ACAGGGTATTTCTGT | 5607 |
rs376567276 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798764 | GAAGAATAAACTCAG[A/G]AAGGTTGATTGAAAT | 5607 |
rs376587393 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768660 | CGAAAGGTATTTTTA[A/C]TAGCAAATGAGAATA | 5607 |
rs376593862 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611986 | TCTCTGAATAACTGA[C/T]TAGCTCAATGTCAGA | 5607 |
rs376594232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804521 | TGAGCAGCCCTCTCC[C/T]CTCGCCTACCGGGGC | 5607 |
rs376616328 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575946 | TTTTTTTAAGATGGA[G/T]TCTTGCTGTGTCGCC | 5607 |
rs376643653 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618031 | TATTCTAGAAATTCA[A/G]TTTATTCTTTGTAAT | 5607 |
rs376648962 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725729 | CAAAAGTCATAATCC[A/G]CAGATCACTGTGATA | 5607 |
rs376691058 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547555 | CTGCCTCCCAGGTTC[A/G]GGTGATTCTCCTGCT | 5607 |
rs376708425 | in-del | -/G/T/TGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756515 | CCCACACACAGTTAC[-/G/T/TGTG]GTGTGTGTGTGTGTG | 5607 |
rs376728076 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623641 | CTCTTGTTGTCCAGG[A/G]GGCTAGAGTGCAATG | 5607 |
rs376752036 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664333 | GATCCCTGTTTCTAC[A/C]AAAAAAAAAAAAAAA | 5607 |
rs376757032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587924 | TACTCGCCAGCATCC[C/G]TGCTGCTGTGTGGGT | 5607 |
rs376758490 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563455 | ATCACAGTTGTCATA[C/T]ATTTTTCTATATAAT | 5607 |
rs376791580 | in-del | -/CTCAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603089 | GTGAAATACACATAA[-/CTCAA]GTTAACATTTTAACC | 5607 |
rs376798342 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632191 | TACAGCCTCCACCTC[A/G]CAGGTCCAAGAGATC | 5607 |
rs376806613 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696843 | AATCAGCTGGGCGTG[G/T]TGGTGCATGCCTGTA | 5607 |
rs376827336 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577228 | GCGTGAGCCACCGTG[C/T]CCGGCCAGTAACCCT | 5607 |
rs376838431 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698468 | GTGCTGGGATTACAG[A/G]TGTGAGCCACCACGC | 5607 |
rs376881929 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629197 | TGACGGGGAAGCTAC[A/G]GGTTACAACAGATTT | 5607 |
rs376882213 | snp | C/G | 0.000131872 | 0.00811902 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67692519 | AAACACAAGAGGACA[C/G]GTTAAGCTGTGTGAT | 5607 |
rs376885526 | snp | C/T | 0.000153988 | 0.00877328 | missense | MAP2K5 | GRCh38.p7 | 15:67772721 | GTATGCGAAAACAGC[C/T]AAAAGAAAGGCCAGC | 5607 |
rs376890979 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604227 | GGCAGGTAATTTTAA[A/G]TTGGTATTTCTTGGA | 5607 |
rs376903824 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741643 | TCCCATGGAACACAC[A/G]GGCTTCTTGGGGGTG | 5607 |
rs376911924 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744021 | GGCCAGGCACTATCT[A/G]TGACTTTGAGCGCTG | 5607 |
rs376916955 | snp | G/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672154 | TTATAGCAGCATGAT[G/T]TATAGTCCTTTGGGT | 5607 |
rs376935501 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675299 | TGATGCCCACAACCT[A/G]GATGAACCTCCAGAT | 5607 |
rs376941796 | in-del | -/TCTT | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542890 | GGCCCTGGGGCTCTT[-/TCTT]AATAGCCCCGGACTG | 5607 |
rs376949819 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760647 | AACAAGTAGCTTTGT[G/T]TTATTTCCTTTGAAT | 5607 |
rs376961581 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617520 | TCTCCTAGAATTTGA[A/C]ATTCTAGGCATAAAT | 5607 |
rs376965256 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748181 | ATCATAATGTGTCCA[A/G]GTGAGTCATTTTGAT | 5607 |
rs376968791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619633 | GTTAGGTAATTAGAG[C/T]CTACAATATAGTTAA | 5607 |
rs376970300 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584695 | TTTTTTTTTTTTTTT[C/T]TGACACAGAGTCTCG | 5607 |
rs376971881 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637441 | AGAGGTAGTACTCTT[C/T]TGAGTACTCTACCTG | 5607 |
rs376983123 | snp | A/T | 1.66543e-05 | 0.00288563 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693469 | ATAATTGCCCATTTT[A/T]TTTCCACATTATCTT | 5607 |
rs377004140 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575515 | TGCACAGGGTGTGAG[C/T]GAAGCCACAGCTCTC | 5607 |
rs377010602 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762368 | CTATGGCTGATGACC[A/C]ACAAGAGACCTAAAA | 5607 |
rs377054587 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670334 | GGAGGAGTTGACTGT[A/G]AAGGCATGAAGGAAC | 5607 |
rs377059057 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649693 | TTGATCTAGTTGTCT[A/G]TCTTTGTACCAGTAC | 5607 |
rs377082004 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577260 | TATATTAGGGTAAAT[A/G]TTTTTATGCTCATTT | 5607 |
rs377092933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631371 | CTTGGATCGGGCTCA[C/T]ATTACCTCCTACCTG | 5607 |
rs377094548 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801308 | GGGCAGTCACCTGAT[C/T]ACAGGGCTGCCCTGT | 5607 |
rs377095556 | snp | C/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651366 | AAACATTTATCATTT[C/G/T]TTTGTGTTAGGAGCA | 5607 |
rs377100961 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613422 | GAGATTACCTATTGT[A/G]TAATGATACATGTGA | 5607 |
rs377101783 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589363 | GGTTGTTTTTTCTTT[G/T]GCCTTAGGTGAATAA | 5607 |
rs377108662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690292 | CTACTGTGGCTATGA[C/T]GTGTTGTGCTAACTA | 5607 |
rs377138239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661533 | CAGATTTCTAGCTCC[G/T]TTTTCACCAGAATTT | 5607 |
rs377140485 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686172 | ACGTTAAGTGTGAAT[G/T]GTCTAAACAGTCCAA | 5607 |
rs377161934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716750 | AGTGCTCTTTCCTCT[C/T]TTCCAAGCTCTTGAC | 5607 |
rs377171184 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756900 | GGCTGAATAAGATTC[C/T]ATTTTGGTGTGTGTA | 5607 |
rs377198671 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672223 | TCTAGTTCTAGATCC[C/T]TGAGGAATCGCCACA | 5607 |
rs377208170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703598 | GAGGTTATTTTAAAG[C/T]ACTGTTTATTACAGA | 5607 |
rs377246048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768546 | ACTCCAAAGCACAGT[C/G]AGATTAAAATAAGTC | 5607 |
rs377264537 | snp | A/C | 5.14584e-05 | 0.00507214 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630849 | TTTTGTAGGTTGTTT[A/C]GTGATCCCAAATGAT | 5607 |
rs377271701 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772421 | CAAAAGTAGAATTAG[A/G]ATACATTTAATTTAA | 5607 |
rs377306013 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712278 | ACTTAAAGATCCAGA[C/T]GTTTGGAGTTCCCCC | 5607 |
rs377320505 | snp | C/T | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541499 | CGTTCTACAACCTTA[C/T]GCACTTTAAAATCTG | 5607 |
rs377323421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607794 | GAAAAGGGTATCTTG[C/G]TTTTATTTTTTATGA | 5607 |
rs377333477 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578899 | CAAACTTGACCCCAA[A/G]CACCAGTTTTAGACA | 5607 |
rs377346438 | snp | A/G | 0.000514668 | 0.0160334 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806916 | CCTGGGGAGCCCCAT[A/G]TGTGGCCCACCCCAC | 5607 |
rs377372257 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769263 | ATTTCACAGCTCTTT[A/G]TTAATTACAAGACCA | 5607 |
rs377372934 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553651 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5607 |
rs377381141 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805697 | ATTCTCTGTCCTCGC[G/T]ATGGCTCCCCGAGTC | 5607 |
rs377386892 | in-del | C/GG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715243 | GGGCGGGGAGGGGGG[C/GG]GTCTAAAATTGTGTG | 5607 |
rs377400904 | snp | C/T | 3.32568e-05 | 0.00407766 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67772747 | CCAGCACCTGAAGAA[C/T]TGATGGTAAGTGAAT | 5607 |
rs377431341 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605077 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 5607 |
rs377438204 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549275 | GTGTTTTCAACTTTA[C/T]AGATTTATTTAAGCA | 5607 |
rs377450309 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584718 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 5607 |
rs377466246 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746812 | CGCCGTGTTCATTTG[A/G]CAAATATATGGGAAA | 5607 |
rs377469020 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765858 | GAGAGTCCAGTTGAA[C/G]TTAACATACATTAAG | 5607 |
rs377476261 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806347 | AGGCAGAGTGTGCAG[C/T]GAAGACAGGCCCTCG | 5607 |
rs377492339 | snp | A/T | 0.000301346 | 0.0122712 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642524 | GGAGACAATGGTGGC[A/T]TTCAAGCTGGGTCTA | 5607 |
rs377497461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636841 | ATTAACATTTGAGTT[A/G]ATGTTAACGTAAGAG | 5607 |
rs377510468 | snp | C/G/T | 0.000131829 | 0.0081178 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550111 | GTATACTTTCTTGAC[C/G/T]ATTCCTTTCTGCAGT | 5607 |
rs377516957 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739385 | CATTTACAGTCAAGC[C/T]AGTAAGACACATGTT | 5607 |
rs377525126 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699057 | ATTTAATGAGGACAT[C/G]AGCTTCTAGTTTCTG | 5607 |
rs377543302 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598133 | TCATTTGAACTTGAG[A/T]TGTGGAGTTTGCAGT | 5607 |
rs377559601 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769730 | TTAACTCGGCAGCTC[C/T]GTGAGACCTTATGGC | 5607 |
rs377567740 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805554 | GCCCAGCCTGTGCAG[G/T]TGGAGGACAGGCCCA | 5607 |
rs377571876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718982 | ATCACCTGTTGTGCC[A/G]TGAATTACTAGAATT | 5607 |
rs377577106 | in-del | -/AAAC | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622945 | CTACTAAAAATACAA[-/AAAC]AAAATTAGCCGGGCA | 5607 |
rs377579034 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765252 | TAGTCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 5607 |
rs377638362 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677302 | GTAATTTCATTAATT[-/T]GAACCTCAATTTCCT | 5607 |
rs377681757 | in-del | -/A | 0.430583 | 0.172886 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541857 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs377696928 | in-del | -/TCT | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711013 | CAGCTGAAGGTAATA[-/TCT]TCTTCTTCTGACCTT | 5607 |
rs377697978 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574835 | TCGTACCGCTGCACT[A/C]CAGCCTGGGCGACAG | 5607 |
rs377699075 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592328 | CTAGATTTTTTGTAA[C/T]ATTTAATTTTTCTGG | 5607 |
rs377706489 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610524 | TGTACCATAGCATCT[A/G]GGGTATTTACTTAAA | 5607 |
rs377747618 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704477 | TGTAACCTTTTTTTT[-/T]AGTCAAATACTTTTT | 5607 |
rs377749654 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588455 | ACTCCCTTCTTCCTT[A/G]TATTGTAGTAGTGAG | 5607 |
rs377751144 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571944 | AGGAGCTCATGGTCC[A/G]GTCAGGGAGATTAAC | 5607 |
rs377751936 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553652 | GGCGTGGTGGCTCAC[C/G]CCTGTAATCCCAGCA | 5607 |
rs377752941 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623844 | TCAGGTGATACGCCC[A/G]CCTGGGCCTCCCAAA | 5607 |
rs386383348 | in-del | -/CCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583974 | GCTGGTGTCAAACTC[-/CCT]CTGAGCTCAAGCAAT | 5607 |
rs386383349 | in-del | -/AAAAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592131 | TCAAAAAAAAAAAAA[-/AAAAA]AAAAGGACTTTCACT | 5607 |
rs386383350 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623605 | TATCTTCCTTTTTTT[-/T]TTTTTTTAGACGGAG | 5607 |
rs386383351 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623606 | ATCTTCCTTTTTTTT[-/T]TTTTTTAGACGGAGT | 5607 |
rs386383352 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664353 | AAAAAAAAAAAAAAA[-/AA]AGCTAGGCATGATGG | 5607 |
rs386784959 | multinucleotide-polymorphism | AC/TA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581875 | CAGGAGTGCTTAGTA[AC/TA]TTACTAGTAACTTAT | 5607 |
rs386784960 | multinucleotide-polymorphism | CT/GG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589256 | AGGATACAATTTTTT[CT/GG]TTTTTTTTTCTTTTT | 5607 |
rs386784961 | multinucleotide-polymorphism | CC/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591780 | CATTATAAAGCTAGA[CC/TG]ACTTAAGAGCTCCCC | 5607 |
rs386784962 | multinucleotide-polymorphism | CT/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592113 | ACAAGAGTGAAACTA[CT/TG]TCTCAAAAAAAAAAA | 5607 |
rs386784963 | in-del | C/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624790 | ATCCGCCACCAGGCC[C/TG]GTTAATTTTTTGTAT | 5607 |
rs386784964 | multinucleotide-polymorphism | AC/GT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673263 | GTTGCAAAAAAATGC[AC/GT]AAGACAGTCCCATCT | 5607 |
rs386784965 | multinucleotide-polymorphism | CAG/GAA | | | intron-variant, cds-indel | MAP2K5 | GRCh38.p7 | 15:67680173 | TTCCTTTTTATTGTT[CAG/GAA]TAGTATTCCATTGTA | 5607 |
rs386784966 | in-del | ATTGGA/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687256 | TGAAAACCAGGCTGT[ATTGGA/T]TTGGTTTCTGGTTCA | 5607 |
rs386784968 | in-del | ATCTCT/TTTTGTGACA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727589 | GCAAAGAGTTTTTAC[ATCTCT/TTTTGTGACA]GTCTAGAAGAAACTG | 5607 |
rs386784969 | multinucleotide-polymorphism | GGT/TGC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741582 | TTGCTGACTAATGTA[GGT/TGC]CTGAACCACCTACCA | 5607 |
rs386784970 | multinucleotide-polymorphism | CT/TC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784784 | TTCTGCCTTTCCACT[CT/TC]TGCCATCATGGGTAT | 5607 |
rs397700233 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656342 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTAC | 5607 |
rs397704322 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725242 | CAGCCATCCTTTTTT[-/T]ACCTTGTACAGTCAT | 5607 |
rs397718945 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655533 | CTTTCATGTTCAAAT[-/AT]GTCATTCCCCTGCCT | 5607 |
rs397721141 | in-del | -/TT | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616187 | GATGCTTCTTTGCTC[-/TT]TGTGTGACATTTTAT | 5607 |
rs397746119 | in-del | -/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786031 | TGTTTTTTTTTTTTT[-/T]AACTTACAGAAGATG | 5607 |
rs397747367 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769119 | AGTAAAAAAAAAAAA[-/A]TTGATCCAAATTATT | 5607 |
rs397762863 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669801 | GATAACAACAAAAAA[-/A]CCTGATAATATGAAG | 5607 |
rs397764140 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656341 | TTTTTTTTTTTTTTT[-/T]TGAGACAGGGTCTTA | 5607 |
rs397776109 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759571 | CTCAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 5607 |
rs397805338 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565640 | TCAAATTCAGTGTTT[-/T]AATTATTTTTGTGTT | 5607 |
rs397810281 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555801 | TTCCTTTTTTTTTTT[-/T]GAGACGCAGTCTCAC | 5607 |
rs397815776 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629406 | TAGATTTTTTTTTTT[-/T]GCACCATGCTGTTGA | 5607 |
rs397841289 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715245 | GCGGGGAGGGGGGGG[-/G]TCTAAAATTGTGTGT | 5607 |
rs397841290 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737564 | AAGTTCATTGAAAAA[-/A]TCAATGAGTTGCCTA | 5607 |
rs397841291 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770042 | CCCATAAAACTGTCT[-/T]GTCACTTAGTGGAAG | 5607 |
rs397938847 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785840 | GCCAAGAAGCAACCT[-/T]GGGAAACTGGAAAGA | 5607 |
rs397946144 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597197 | AAAGAAAAAAAAAAA[-/A]CTACTTGGTATTGTT | 5607 |
rs397960657 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635203 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 5607 |
rs397960810 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796701 | TACATTGGTTTGGAA[-/A]TCATATTCTGTTTCT | 5607 |
rs397964561 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765370 | TAATAAAATTTTTTT[-/T]AAAAAGTATAGTACA | 5607 |
rs397970918 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741912 | TTTTTTTTTTTTTTT[-/T]GAGAGGGAGTCTTGC | 5607 |
rs398027745 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550789 | GTGAGAGTCTGCGGC[-/A]AAAAAAAAAAAGAAA | 5607 |
rs398027747 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556569 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 5607 |
rs398027748 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595989 | TAAAATCTAAAAAAC[-/A]AAAAAAAAAAAAGAA | 5607 |
rs398027749 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621449 | AATTAACTTTTGTTC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs398027750 | in-del | -/A | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690552 | AGCGAGACTTGTCTC[-/A]AAAAAAAAAAAAAAT | 5607 |
rs398027751 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741048 | TAAAAGTGCATTCAC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs398027752 | in-del | -/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752910 | TGCAACATTGTTTTC[-/T]TTTTTTTTTTTTCAA | 5607 |
rs398038167 | in-del | -/T | 0.5 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709494 | AGTTTAGCCCTGTAG[-/T]TTTTTTTTTTTTTTT | 5607 |
rs398057780 | in-del | -/CCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627022 | ACTGCAGCCTGACCT[-/CCT]GGACTCAAGCGACCC | 5607 |
rs398057782 | in-del | -/CT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683754 | GACATGAGCAAGACT[-/CT]GTCTCAAAAACAAAA | 5607 |
rs398057783 | in-del | -/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780284 | TACTTTTTTTTTTTT[-/TT]AACCTTTAAAGTTCT | 5607 |
rs398078272 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648589 | GTTCTTTTTTTTTTT[-/T]TGAAACAGAGTCTCG | 5607 |
rs398078273 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653301 | TATTTTTTTTTTTTT[-/T]TGAGACGGAGTTCTG | 5607 |
rs527243612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791245 | GCATTAAACAGGAAA[A/G]GGGGCATTGGAGTTG | 5607 |
rs527246503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695118 | CTGTTGTGGGTTGGG[A/G]GGAGGGGGGAGGGAT | 5607 |
rs527246550 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779059 | TTTGTTTTCAGTTGT[C/T]CATTTGGAAGTAGCT | 5607 |
rs527263905 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584098 | CAAGTAGCACAGTTG[C/G]CTTGGATAGTAACTC | 5607 |
rs527276949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737945 | CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 5607 |
rs527279016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707773 | GAGAAAGAGGGAAAA[A/G]ATAGAGGATCTCTTC | 5607 |
rs527292373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638915 | GCCCACTTTTTAATG[C/G]GGTTGTCTTTTTCTT | 5607 |
rs527292595 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674685 | GAGATCAGAAACGCT[A/G]CATGTCTTAAAAGTA | 5607 |
rs527329490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576381 | ATAACAAATATGAAC[A/G]CTGTAGTAAACTTGC | 5607 |
rs527338234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731486 | TGGGTTGCATAACTT[C/T]CTTGGCATGCAGTTT | 5607 |
rs527345636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790736 | ACAAACAAACAAAAA[A/C]AAAAAAACCTGTGTC | 5607 |
rs527345652 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636563 | TTTCATATCTTATAA[-/T]TTTTTTTTAAGTGAA | 5607 |
rs527349350 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707016 | CGCCTCCCAGGTTCA[A/T]GTGATTCTCCTGCCT | 5607 |
rs527361657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632632 | CTCTGATCTTCATCT[A/G]TCTTTTCATGGTTCA | 5607 |
rs527373461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545784 | GGGTGAAAGTAATGC[C/T]TACCTCCTAGAGTTC | 5607 |
rs527386509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688052 | TAAAAAGGTAAGAAT[C/G]TAAAGCAAAGGAGAA | 5607 |
rs527440869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730839 | CTATTGGAAGGAGCC[C/G]TGGACCATGAGCCAG | 5607 |
rs527443113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639556 | CGGTGACCCCCCTGC[C/T]GGCGCTGCTCACTGC | 5607 |
rs527460484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673058 | CATGCTGTTTTGTTT[A/G]CTGTAGCCTTGTAGT | 5607 |
rs527491774 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778845 | GGTGCATTTCCATAG[A/C/T]CCCCTTAGAGAGTGC | 5607 |
rs527500317 | in-del | -/ACTT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629777 | TTTTAGTTCTTCGAA[-/ACTT]ACTTACTTCCTTATA | 5607 |
rs527507528 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553870 | GTGAGCCGAGATTGC[A/G]CCACTGCAGTCCGCA | 5607 |
rs527523167 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701541 | AGGAGTAGAGAAAGG[C/T]TTCACCCTCAAACAG | 5607 |
rs527532003 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767521 | TTCCTCACTGATCAG[A/G]GTCCATCATTTTTAC | 5607 |
rs527563231 | in-del | -/TAGACA | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683893 | GTTATCTTCAAACTT[-/TAGACA]ACAGGCAATGTGAGA | 5607 |
rs527572621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612461 | ACTTTCCTTCTGTTG[G/T]CCAGAACATAGCTCC | 5607 |
rs527581424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710290 | GAACAGTCTGGCTCA[A/G]TGTGCTTGGTTAATT | 5607 |
rs527583539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718444 | GAGATGGGGTTTGGG[A/G]CAGTTAACTCTAATC | 5607 |
rs527586718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771389 | AACCTGGGGGTGGGG[A/C]TGGTCTGAGCAGCAG | 5607 |
rs527593816 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576968 | GAGTCTCGCTCTGTC[A/G]CCCAGGCCGGACTGC | 5607 |
rs527608248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673676 | GTATTGCTATCAATA[A/G]AAAACTAACCTGATT | 5607 |
rs527609508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674613 | TTGGTCATTCATTCT[A/G]TTTACCTTGGGTGAT | 5607 |
rs527635668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624327 | CTGGGCGACAGAGCA[A/G]GACTCCGTCTCAAAA | 5607 |
rs527637955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617147 | TCCGTGCTCATTTTG[A/G]TAACTATTTTGCTAA | 5607 |
rs527652632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575054 | GTCTGATAGGGGATA[A/G]GAGAGGAAATCAGTT | 5607 |
rs527658992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567184 | ATTCAGCAGCCAAGT[C/G]TTATTACAGCACCAT | 5607 |
rs527662184 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714204 | AGGAAGATTAGAAAT[A/G]TATTCAATATTCTAG | 5607 |
rs527665534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679612 | TTTATCAGGCCTAGA[A/G]CATATCAGTTCTAAG | 5607 |
rs527698103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624068 | AGCTAGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 5607 |
rs527701032 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630446 | GTGTAATTAAAAAAA[A/T]AAGCAAAAAAAATGG | 5607 |
rs527704261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722065 | TAATGTGGAGGGTCC[C/T]AAAGGTTATTAGGGC | 5607 |
rs527718866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783066 | AGAAGCCTTTTCTAC[C/T]GTTGTGAGACATGGA | 5607 |
rs527719567 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775456 | ATCAGAAGTGCTCTC[A/C]AAAGTTTTATCAGCA | 5607 |
rs527722380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686465 | TACAAAAACTAGCTG[A/G]GGGTGGTGGCAGGCG | 5607 |
rs527725629 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710921 | CGCTGTTCTCTGTAC[A/T]TGTAATATCATTTTT | 5607 |
rs527725830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678761 | ATGAGGTCAGTAGTT[G/T]GAGACCAGCCTGGCC | 5607 |
rs527735764 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747068 | CAGATGCTGGAAGGA[A/C]AGGAGCTCTGGAGGA | 5607 |
rs527773647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618047 | TTTATTCTTTGTAAT[A/G]ATGTATCTTTTAATA | 5607 |
rs527779027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715997 | AGACACAGATATAAG[G/T]TTAGACAAGATGCAG | 5607 |
rs527779470 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634006 | AACTTAAATTGTTTT[-/A]AATTTGTTGAGACTT | 5607 |
rs527783113 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768677 | AGCAAATGAGAATAG[A/G]TGAGAATGGAGTCAT | 5607 |
rs527791641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583089 | CTCCTGATAGTTCTG[A/C]CTATTAGGTATTACT | 5607 |
rs527797040 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560282 | AGCTTTTGCCTTTTG[G/T]CTGGAGCCACCAGTC | 5607 |
rs527800175 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743740 | TATCCAGCACAGTGC[C/T]AGATAAAATTAGATT | 5607 |
rs527800812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670311 | ATCACTGGTTGACAA[A/G]CAGTGGAGGAGGAGT | 5607 |
rs527817832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722790 | GATTTAACTGCAGCG[C/G]ACAATCTAAATGCAA | 5607 |
rs527847179 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561249 | TATGTAACATTACAT[A/C]ATTTGTACTTTGTTT | 5607 |
rs527853328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701198 | TTAGTTATTTCTTTA[A/G]TAATTCTAGAGGATT | 5607 |
rs527856463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709310 | AAGAAAATAAAAAAG[A/G]AGTGAGACCCACTAA | 5607 |
rs527874988 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611280 | TAAAATACATGGGAT[A/G]AAATTATAGAATGAA | 5607 |
rs527885785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662376 | GATATGTAAACGACT[A/C]ATTTACTTCTCATGG | 5607 |
rs527886080 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587688 | GTTAAGCCCTCAGAA[C/T]GTGGTTGTTCCCTCT | 5607 |
rs527886615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716558 | CTAGAAAATTCTCTT[A/G]TATGCCTTATGTTGT | 5607 |
rs527911112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610502 | ATATTGCACAAGCAA[A/G]TATTTGTGTACCATA | 5607 |
rs527911295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761380 | ACTATAGCACAGTTT[C/G]ACGTATAATTCTCAG | 5607 |
rs527916805 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544928 | CGGAGTTCTCCACAC[A/T]GTCATGCACATACAG | 5607 |
rs527918478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769909 | CTGCTGAAAGTCATG[A/C]TACTTCTTTAAGCAC | 5607 |
rs527924536 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585368 | TGCAAGAAATGTAAT[A/G]AAATTAGTTATATAT | 5607 |
rs527959560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645932 | AATGTGGCTAAAATA[C/G]AGTGCATAAATTAAG | 5607 |
rs527966705 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798664 | CCCTTAGGTGCCTGC[A/G]TACTGTCTAGGATGG | 5607 |
rs527970330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701722 | CTCTAGCCCCACCCC[C/T]AGAGATTCTTATTCT | 5607 |
rs527975573 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798557 | GACACCTCTGGAAAC[A/T]TTTTTTTTCTCCCAG | 5607 |
rs527989814 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560417 | GTCTCCCAAAGAGCA[C/G]TTTGTAAAGAAAACC | 5607 |
rs528041808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614047 | CAGAGAATGTTGAAG[A/G]CAACTGAAATTAGAG | 5607 |
rs528055828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675749 | ACCTGTATTCAGAAG[A/G]TCAGCTTAATCAGAG | 5607 |
rs528073508 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566705 | GAATTACTTTTTCCC[C/G]CTCTTGGATGCAGGC | 5607 |
rs528096979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726771 | TTAGCGTTAAAGTCC[C/G]TGATGTTGCGATTCT | 5607 |
rs528106765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780215 | TTTAAAAGGCTAAAG[A/G]AAAAAATGCCTGGAT | 5607 |
rs528107560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628191 | GGTGGCATTAAAGAA[G/T]ATACTGAAGGCTGGG | 5607 |
rs528109174 | in-del | -/AAAATAA | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651650 | CAGATTATTTCATTT[-/AAAATAA]TATCCACCCATATTC | 5607 |
rs528112448 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595200 | AGCTTTCTGCCTGGG[G/T]TCATTGATATAGGTT | 5607 |
rs528125674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772220 | GACCTGTTTTATATA[C/G]TTCTTGTCATTCGGA | 5607 |
rs528132184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674936 | CAGAATGGCTAAAAT[A/G]AAAAATAGTAACAAT | 5607 |
rs528143752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657464 | AATGAGAACATAAAA[C/T]GTTTTTCTGCTGTAT | 5607 |
rs528155632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757933 | GACTGAAGGATAGCC[A/C]ATAAGAGTTAGCCTT | 5607 |
rs528164237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614637 | TCCTTGATCTCAGAG[A/G]TATTTAGACCATATA | 5607 |
rs528172935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712783 | ATTAGCTGGGTGTGG[A/T]GGCAGGTGTCTGTAG | 5607 |
rs528183624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579515 | TTTTATGTCTGTAGA[A/G]GGAGAGAATCACTTT | 5607 |
rs528183884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571081 | ACTATGTCTATATCA[A/G]TTCCTCTCTGGATTC | 5607 |
rs528188065 | snp | A/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682412 | GTATTTTTAGTAAAG[A/T]CAGGGTTTTGCCACG | 5607 |
rs528188325 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666163 | AAGTGAGTGTTAGGA[A/T]CATCCTGTCTCTGGG | 5607 |
rs528237579 | snp | C/T | 1.68596e-05 | 0.00290336 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600641 | CCTTGACATTTCCAT[C/T]CACAGCATGACACCC | 5607 |
rs528256774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608403 | GCATGTGCTGTGTGG[A/G]GGGCGTGTCAGATGT | 5607 |
rs528262636 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649232 | TCTATTTTTTAAATG[A/G]GTTATTGGGCTTTTA | 5607 |
rs528282729 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658220 | CAAAAGACAGGCAAC[G/T]AAATGTTTAATAGTC | 5607 |
rs528283345 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713494 | TAATCCCAGCACTTT[G/T]GAAGGCCGAGGCGGG | 5607 |
rs528296223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801776 | TACAGAATATAGAAG[C/T]CACCTTTTCATGAGG | 5607 |
rs528315006 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541557 | AGGTTGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 5607 |
rs528315379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549972 | TATTTCCTGTAGGAT[A/T]TGCCACATGTTAGCA | 5607 |
rs528322586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742186 | GTGAGCCACTGCGCC[C/T]GGCCAAGAAAGAACT | 5607 |
rs528335354 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645437 | GAACCAAGATCGCCC[C/G]ACTGCACTCCAGCCT | 5607 |
rs528338310 | snp | C/T | 1.77112e-05 | 0.00297578 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642517 | GCTTCATGGAGACAA[C/T]GGTGGCATTCAAGCT | 5607 |
rs528364648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698347 | CGTGCACCACCACGC[C/T]CGGCTAATTTTTGTA | 5607 |
rs528392525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593316 | TTGGGGAGAAAAGGA[A/G]AAACCATTACTTTCT | 5607 |
rs528396571 | in-del | -/CTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576026 | TGGGTTCAAGCAATT[-/CTC]CTGTCTCAGCCTCCT | 5607 |
rs528420173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650670 | CCAGTCTTGCAGTGT[G/T]GGAATTATTCCACTT | 5607 |
rs528437841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799950 | AGAGTGGGGGGCGGT[C/G]GGGGGGATTGTTATT | 5607 |
rs528447404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806590 | AGGCCCTGGAAAGTA[C/T]AATGAGCGCGGGAGT | 5607 |
rs528457612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655510 | GAATTTTTGGTTTAT[A/G]ATCTTTTTCTTTCAT | 5607 |
rs528460154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703617 | GTTTATTACAGATCA[C/T]CTGTGTAAGACCTGC | 5607 |
rs528468315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756018 | TCCCCATTTTTCAGC[C/T]ACAAACCTAATGGAG | 5607 |
rs528470064 | snp | C/G | | | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658588 | AGGAAAATGCCAGAA[C/G]ATGTCCTTGGAAGAA | 5607 |
rs528488479 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547607 | ATTACAGATACACAC[C/T]ACACATCCAGCTAAT | 5607 |
rs528502456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613043 | TGTTGTTCTGAGATG[A/G]GACAATTCCCCAATC | 5607 |
rs528503899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711096 | ATTTATAGGCATGTC[A/G]TAGTTCCTTATGACA | 5607 |
rs528528494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648710 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5607 |
rs528532004 | snp | C/T | 0.000214864 | 0.0103627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748304 | TTTTCTTTTTCCTGA[C/T]GGCTGCTTCCTTTGC | 5607 |
rs528532321 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693131 | CCTCCAGCGTATTTA[A/G]TGTTCATTTCATTCT | 5607 |
rs528532961 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625447 | GGTAATTACTGTGGC[A/G]ACAACAAACTAATTT | 5607 |
rs528546648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792414 | GGGGCTACCAGGACT[A/T]GAAAAATGTTGCTCT | 5607 |
rs528549607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739646 | CCACCACACCTGGCT[A/G]ATTTTTGTATTTTTA | 5607 |
rs528561708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704548 | GGAAATAATCTTCAA[A/G]CTCAATTCACCTGCA | 5607 |
rs528621747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756805 | GTGTTTCTGTGTCTG[A/T]CTTACTTCACTTAGC | 5607 |
rs528628576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689952 | ACATGAGCCACAGGA[C/T]GGCTTTGAGTAGTGC | 5607 |
rs528640028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747501 | TTAATTTTTATGTCA[C/T]GTTTTAGTAGCTTTG | 5607 |
rs528641864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786098 | GACATACATGGGGCA[C/T]GAGGTCATTCAGCCT | 5607 |
rs528642545 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691646 | AGATGCTGCTCTATA[C/T]CATCAAAAGTGGTAT | 5607 |
rs528688545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689276 | ATCATATGCTTTGTC[C/T]CATATGTTACATACA | 5607 |
rs528702606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720842 | TTATCCTCCTGCTGC[A/G]CTGGGATATAACCCT | 5607 |
rs528709317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793091 | AAATGTGTTATAACA[C/G]TGCTCTATCCTCTTA | 5607 |
rs528722865 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722678 | GGATGAAATCTCACC[G/T]AGGGAATTTTATGTA | 5607 |
rs528726023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591828 | TTCAATAAGGACTTT[C/T]ACGCCAGGGGTGGTG | 5607 |
rs528735442 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755410 | AGAAATATTAGCTGC[C/T]CCTTAGTCTGCCTGA | 5607 |
rs528738731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599638 | ATTGAATTAAAAACT[C/G]CATCCATTTTCTGCC | 5607 |
rs528744246 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717648 | GCAAGGCCCAGCCAT[G/T]CTATGTAGCATCAAA | 5607 |
rs528753472 | snp | C/T | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542517 | CAAGACCAGTCTCTC[C/T]CCGACTCGCCACGCG | 5607 |
rs528771577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627807 | TTTCTGCTCGTGGAC[A/G]CCACAGAGGAAACAT | 5607 |
rs528795899 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797233 | TAAAAATCATTACTG[C/T]AGTTGTGGCTTTATA | 5607 |
rs528799617 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753321 | CACCAAGAGCACAAG[A/C]AAACAAAAACAAAAG | 5607 |
rs528800894 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786679 | AGAAAGCCAGCTTCT[C/G]CCCTCCCTCTCCCTT | 5607 |
rs528801571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779714 | TCTCTAATGCCTCTT[C/T]CGTGTTTTATTGGAC | 5607 |
rs528831463 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796301 | TTGCTACAAAGAAAC[A/C]CCTGAGACTGAGTAA | 5607 |
rs528836476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620640 | ACTGTATAAGACAAC[A/G]ATAGTAATAATTCAA | 5607 |
rs528839470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771491 | GGAGACAGAGGGAGG[G/T]ATAACCTGCATTCAA | 5607 |
rs528844063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586716 | ACTGAATAGACTCCA[A/G]CTGTGGGTTTGTCTA | 5607 |
rs528851000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779676 | GACTTGCCTGTTTAA[C/G]ATTGTAGTTATTTGA | 5607 |
rs528859990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578615 | TAAGTGGCATACTTG[A/G]TATCATTACTGTGAC | 5607 |
rs528876072 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662546 | CCTTGAAATTGGTAA[G/T]TTCACGCTCATGTGC | 5607 |
rs528876629 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619591 | GTAGAACATAACATA[G/T]ACCCTATATTAAGAA | 5607 |
rs528899612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626997 | TAGTGGAGTGGTGAG[A/G]TCATAGCTCACTGCA | 5607 |
rs528905205 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586046 | ACAAGCGATCCTTTT[A/T]TTTTTTTTAAATGGG | 5607 |
rs528914435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634339 | CACCACTGCATTCTA[C/G]TCTGGGTGACAGAGT | 5607 |
rs528926315 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735346 | AATTGAGATATCTGT[A/G]TTTGGCCAGTTAGGT | 5607 |
rs528928582 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681812 | ATTTGTATTTTCTTT[A/G]AGAAAATGTCTCAGT | 5607 |
rs528935552 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732442 | ACAGGAAAGTGAAGA[C/T]AATACAGACACAAAT | 5607 |
rs528937261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779138 | TGTAACTTCAGCTGA[A/G]TATTTCCATCATGCA | 5607 |
rs528940933 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696963 | CAGCCTGGGCAACAA[A/G]AGTGAAACTCAGTCT | 5607 |
rs528957629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665224 | TGAAAGCATCAGGAA[C/T]AGTCCCCTTGTCTAG | 5607 |
rs528984010 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643136 | CCCTAGGTATTACGA[C/T]ATGAGGCCAGGGTTG | 5607 |
rs528988225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725950 | TCCCTTTTCCCTCCC[C/T]GTACATAGACAACAA | 5607 |
rs528996725 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762091 | TCATTTAATGGTTCC[A/T]AAAACTCAATCTTGT | 5607 |
rs529018909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606562 | TCCTCCTTTCTGTTG[A/C]CTTATCTAAAAAGAG | 5607 |
rs529022287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664724 | TGATTTTTAAAGTAA[C/G]TGTTCTGACATTTAA | 5607 |
rs529048956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712700 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCA | 5607 |
rs529062727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719772 | AAAACTGCCCTCAGT[A/G]TTGCATTTTGAGCTA | 5607 |
rs529072842 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800920 | AGCTGCAAAAAGTAA[C/T]ACCACAGTACAAGGT | 5607 |
rs529080191 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790758 | ACCTGTGTCCTAATG[A/T]CTGCCACACTTAGTG | 5607 |
rs529080904 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757151 | TGGCTATACCAATTT[A/G]CATTCCCATGAACAG | 5607 |
rs529082296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613917 | TTTAGTGTTCTAGAA[A/G]AGGTAATTTAGTAAA | 5607 |
rs529084854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656528 | GAGATGGGGTTTTGC[C/T]GTGTCTCCTAGGCTG | 5607 |
rs529092778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711854 | TGGTGGGACGAGATA[C/T]GTGGAGCCAGGAGTC | 5607 |
rs529100553 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545249 | GCAAAGCACATGTTT[A/C/G]ATCATGATTCTTTGT | 5607 |
rs529100568 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575401 | GGGGGAGTGGTTGTT[A/G]CCAAAGAAAGAGCCA | 5607 |
rs529114072 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759036 | ATTCTATTCTGTGTA[C/T]TCTGTTTAATTTGGC | 5607 |
rs529125810 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556864 | AGCCCTTGTTTTTCT[A/T]AATTCTTGCACCATC | 5607 |
rs529138417 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573066 | GGTATCAGGACATTC[C/T]TGAACCTGGGTATGT | 5607 |
rs529182990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757823 | AGCCATATAAATTCT[A/G]TAATTAAAGTGTGGC | 5607 |
rs529188576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801725 | CATTCAGCCAATGCC[G/T]GTACACAGCAAGTGC | 5607 |
rs529197181 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601431 | ACTTAATAGTCTGCA[A/G]TGGTGTATGAAAAAT | 5607 |
rs529202796 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563979 | ATTTCTAAAGCTTCA[A/G]TACTAAGCTTGAAAA | 5607 |
rs529217818 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562604 | CATTTGAAGCTTTCT[A/G]TGGCTGGAGAGTATG | 5607 |
rs529236614 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604733 | AACCCCGACTCTACT[A/G]AAAATATAAAAATTA | 5607 |
rs529255242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710244 | TGCCTGTTTGCCACC[A/C]CTCTAACCAGTCTCC | 5607 |
rs529264418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612296 | GATTGGAGAATAACA[A/C]CTTCCCTTGACTAAC | 5607 |
rs529271149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654020 | CTACTGTGGTTAAGT[A/G]AAGTATCCTTTACAT | 5607 |
rs529275619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554530 | AGTGAGTGGAAAAGA[C/G]GGGAAAGGTCAGGTA | 5607 |
rs529278922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762900 | CCGTGGTTCCAGGCC[C/T]ATCTGAGACAAGTTA | 5607 |
rs529281867 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582524 | TTGCAGTATCCTGGA[G/T]AAATATACTTCCAGG | 5607 |
rs529296137 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564512 | TTCTGCCAATAGTTT[C/T]AATTTAGGGTAGGAG | 5607 |
rs529299000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762380 | ACCAACAAGAGACCT[A/G]AAATAAAAAGAGAAA | 5607 |
rs529325651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619854 | GAGGATCATTTGAGG[C/G]CAGGAGTTCAAGACC | 5607 |
rs529335089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806087 | ACCCAGAGATCCTGT[A/G]CACAGCCCAGCACAT | 5607 |
rs529338758 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655451 | TTATTTGAGAGTATC[G/T]TAATTTCTCCTTCAG | 5607 |
rs529347473 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561581 | GATCTTGATGATACC[A/G]ATTCACACTGAGTTG | 5607 |
rs529373567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569071 | GTTTAAAAGTTTTGT[C/G]CTTACCTACAAGGCT | 5607 |
rs529379288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755954 | TGACTCAATTGTCCA[A/C]CCTCTTTCCATTGTC | 5607 |
rs529386563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605247 | TTTAGTAGGGATGGG[G/T]TTTCACCATGTTGGC | 5607 |
rs529403528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796445 | GCAAGAGGGGAGCTG[A/G]CACATCACATGGCAA | 5607 |
rs529416503 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754851 | AGGTGTTACCCTGTA[G/T]CCAAGGGATATGCTT | 5607 |
rs529416581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794324 | TTGCTCAAGGCTAAG[A/G]GTGAGTTCTATTGAT | 5607 |
rs529417608 | snp | C/T | 0.0205511 | 0.0992634 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547473 | TTTTTTTTTTTTTTT[C/T]GAGACAGAGTCTCGC | 5607 |
rs529420929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591179 | GTGAAACCCTGTCTT[C/T]GCTAAAAATACAAAA | 5607 |
rs529438831 | in-del | -/TA | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594197 | GTAGTCTCAACATTT[-/TA]TAGATAGTATTTATC | 5607 |
rs529451330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738518 | GATTTCTACCCAAAC[A/G]TACGCACAGAGCTAA | 5607 |
rs529472662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647877 | CTGTCTTAAAAAAAA[G/T]AAAAAAAGGAAAATT | 5607 |
rs529504911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703556 | ATAAAGTCTTTGATT[A/C]CTTGTGTGGCTTGTG | 5607 |
rs529518805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639706 | CCTCCACGACATGTC[A/G]TCAGTCTGCTTTTAT | 5607 |
rs529521955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740447 | GATATGTGACAACTT[A/G]TCTTCACATGGGCAC | 5607 |
rs529536790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555059 | TTAGGGCTGGATGAG[A/G]AGAGGGACATCTGTC | 5607 |
rs529553243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732752 | ATGGAGCTCCAGACA[A/T]TTCACCTGGAGGCTG | 5607 |
rs529578861 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667653 | CTTAAAAACCAGAGT[-/A]AAAAAAAAAAGAAAT | 5607 |
rs529596957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689117 | CGTTAAAGCTGAGTG[C/T]AGTGGCAAACATCTG | 5607 |
rs529614973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803103 | GCCACAGTGAGCATG[A/G]GAGCCAGTGGGCACA | 5607 |
rs529638716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659757 | GAAAAAGAAAAAAGT[A/G]TACAACTTCTATATA | 5607 |
rs529641429 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739380 | AATTTCATTTACAGT[A/C]AAGCCAGTAAGACAC | 5607 |
rs529641964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545139 | CACCGGTCAATTCCC[A/G]CCTGTCCTTCCAAGC | 5607 |
rs529650326 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759504 | GGTGGAGGTTCCGGT[A/G]AGCCAAGATCACGCT | 5607 |
rs529659992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640348 | GACCATTGCTCTCAC[C/T]CAGAATATTTCTTAG | 5607 |
rs529671143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550743 | TTTTTTTTTTTAAGA[A/T]GAGGGCTACTTTTTT | 5607 |
rs529698025 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711800 | AATACAAGCAAGCAG[A/G]CAATCTGATATATTG | 5607 |
rs529701463 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612768 | GCGAAAGTAAATAAA[C/T]GAATGGACAGCAATC | 5607 |
rs529708232 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678812 | CTACTAAAAATACAA[A/C]AATTAGCGGGGCATG | 5607 |
rs529714771 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666596 | ATCCCTGGTTGCAAC[G/T]TGGGCTAAGAAAGGG | 5607 |
rs529723635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759064 | GGCATGGAGGAGCGC[A/G]AATCCTTTTAGAAAG | 5607 |
rs529728520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803903 | TGGGTTACAGACTTG[C/T]GGTTCAGTCCCATGT | 5607 |
rs529728888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643537 | CTGGAAGCTCCGCCT[C/T]CTGGGTTCACGCCAT | 5607 |
rs529764590 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598205 | TGAGACTTCATCTCC[-/A]AAAAAAAAAAAACTA | 5607 |
rs529768082 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652226 | GGTGTGTCATTAGTG[C/T]GTGTTTTTTTTAAAT | 5607 |
rs529784906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752234 | CCACACCTGGCCAAT[G/T]TTTTGTATTATTAGT | 5607 |
rs529798813 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566257 | TCGGCTCACTGCAAC[A/C]TCCGCCTCCTGGGTT | 5607 |
rs529806424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693133 | TCCAGCGTATTTAGT[G/T]TTCATTTCATTCTAG | 5607 |
rs529811664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789133 | TTTTTATTCTGCACC[C/T]TGCTTTTTTACTTAG | 5607 |
rs529815313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602369 | CCTTTATGCTGATAG[C/G]CAAATATAATAAAAC | 5607 |
rs529820501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675334 | ATACTGAGTGAAAAA[A/G]CCAGTCACAAAGGTT | 5607 |
rs529826265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588415 | CCCAGTGCACACCAG[G/T]GACCTCTCTAGGAAT | 5607 |
rs529853724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543974 | GCAGTGCTGTGGCAC[A/G]ATCTCGGCTCACTGC | 5607 |
rs529873481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596046 | TTCCTGATAAATCAA[C/G]TATAAATCTACTCAG | 5607 |
rs529884719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595342 | TTCCGATTAGTCTCT[A/G]CTCTATAAAGTGGGA | 5607 |
rs529885196 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796971 | ATTGTGTCTGTTCAC[A/G]TGGCGCTGGCCAAAA | 5607 |
rs529887176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582549 | TCCAGGCAGGGCACA[A/G]TGGTTCATGCCTGTA | 5607 |
rs529898385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743893 | GCCCCACTGAAGGGA[G/T]GGGGCTTCTGGGGAC | 5607 |
rs529904840 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704326 | AACTCTTGGGCTCAA[A/G]CAGTCCTCCTGCCTG | 5607 |
rs529910159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644074 | AATTGTTTTCCACCT[A/G]TTCTATTCTCATCAC | 5607 |
rs529942189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685922 | TGCACTACATCAGCA[A/G]AATTTGAGTAGTTAC | 5607 |
rs529948732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788453 | CATTATTGAAGGTAG[A/T]TGGGTAAGAGAGTCA | 5607 |
rs529964738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782603 | TCTATGAAGGGCCCC[C/T]GTGTTTAAACGGGCT | 5607 |
rs529987271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736199 | GGGACCAGATAAAGA[A/C]ATTGGGTTTGAGAAT | 5607 |
rs529997567 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541332 | TAATCAAGCACCTTA[C/T]TGTTAGAAGGGAAAC | 5607 |
rs530019699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593279 | GCCCTGCATTCTGAG[A/G]TGACTGTTTCTTTCA | 5607 |
rs530020218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741662 | TTCTTGGGGGTGGGG[A/G]AGTGTTGTTGGAGTA | 5607 |
rs530025848 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686402 | ACGTGAGTTCAGGAG[C/T]TCGAGACCAGCCTGG | 5607 |
rs530050655 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735517 | GAGCACAAAAATGAA[A/G]CAGATGTGGTCTCTG | 5607 |
rs530051379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642049 | CATTTTGGAATCTCC[G/T]CTATTCTAGACTAAA | 5607 |
rs530062966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786830 | TAGCACAGTGTCTGG[C/T]ATAAAATAAGTGTTC | 5607 |
rs530084603 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645712 | CGATCATACTACACA[A/C]AGGTAATTTTTTTTT | 5607 |
rs530085005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698249 | GGCTGGAGTGCAGTG[G/T]CGATTGCAGCTCACC | 5607 |
rs530101951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734826 | TTTTTGTATGTGAGG[G/T]CTTTAATCAAGGAAA | 5607 |
rs530112991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780481 | CTCTAATCCAATCCA[A/G]TAAAACACTGTGCAG | 5607 |
rs530115363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787149 | AGGCAGGGCGGACAA[C/G]AGGACTGATTCCGCC | 5607 |
rs530120133 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542154 | CTAATGTGGGAGAAA[A/G]ATGATGATCCTCTGA | 5607 |
rs530129021 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610337 | TGTCCTTATTTACCA[A/G]AAACTTATAATTTAA | 5607 |
rs530161707 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765335 | CTGCACTCCAGCCTG[C/G]TGACAGAGCGAGACT | 5607 |
rs530165520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727062 | AAATTAGCTGGGCAT[C/G]ATGGTGTGCGCCTGT | 5607 |
rs530186858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773727 | TCAGTTTTCAGGGTA[A/G]TTTCAAGTTAAAGAT | 5607 |
rs530190384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622845 | GGCTTACGCCTGTAA[C/T]CCCAGCACTTTGGGA | 5607 |
rs530215737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676633 | TAATCATTTTCCTAA[C/T]ATCATTTATTGAGTA | 5607 |
rs530216175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683617 | AAGTACAAAAATTAA[C/G]TGGGCTTGTTGGTGG | 5607 |
rs530222465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594004 | GCCTTAAAACAGTGC[C/T]GTATGGTAGTGCTTC | 5607 |
rs530224974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691658 | ATACCATCAAAAGTG[G/T]TATGCTCTTGTCCTC | 5607 |
rs530247412 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628774 | TGGCTCTGGAAACTT[C/T]GGTGGTGGTTGTGGA | 5607 |
rs530257632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734440 | AAATTGTGCTCTGGA[G/T]AGAGTATGTGTTTCA | 5607 |
rs530259745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642483 | TAGAGATGAATTTTG[A/G]TGGAGGACTTTGAGG | 5607 |
rs530262581 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590884 | GCCAAGTCATTGGGC[C/T]ATATTTAAGGGTGAG | 5607 |
rs530321094 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615583 | AGAATACTAAAATTT[A/C/T]GAAGCTTGGCCATTA | 5607 |
rs530324658 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804591 | CTTCTGGAATGTGGA[A/G]GAACGCCTCTACGCT | 5607 |
rs530348973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667165 | TTAGAGGTTTTGTCC[A/G]TATTTAATAACTTGG | 5607 |
rs530392819 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713671 | AACCCAGGAGGCAGA[C/G]GTTGCAGTGAGCCGA | 5607 |
rs530400717 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785433 | GCAGCAAGCAGTTCA[C/T]AGGACGACTACTTGA | 5607 |
rs530414637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713757 | AAAAAAAAGTGGCAT[C/G]GATCACCCAGCCCAG | 5607 |
rs530421965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666851 | ATTTCAGTGAATGAG[A/T]GTGCACCTACATCTG | 5607 |
rs530422022 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542763 | CAGCCGCCGCCAGTC[C/T]GCGCGGCCTCGGGTG | 5607 |
rs530429386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580654 | GGCTGATATGTATAT[A/G]CCAGCAATTTACAAA | 5607 |
rs530434215 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801437 | GAGAGGATGTGCTTG[A/G]TGCTCACCCTGAGGC | 5607 |
rs530444850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677510 | TCTTCGGGACACACC[A/G]CTCCAAGTCAAGTCT | 5607 |
rs530445014 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588001 | CCCTCCGTTCTTGGC[C/G]CATTCAGCCCCTCCT | 5607 |
rs530450642 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773542 | TTTACAGATACCAGT[G/T]TAGAGGTTTTCGTCC | 5607 |
rs530456804 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569092 | CTACAAGGCTGTGTT[C/T]TACCTTGTTTACCAA | 5607 |
rs530457590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728365 | TTTGCTAGGCAAATA[C/T]ATAGGCCCCCAATTT | 5607 |
rs530474482 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615388 | GCAAAGACTGCTATT[A/T]GAACTAGTATAGTTT | 5607 |
rs530521570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608427 | CAGATGTTGGGGACA[C/G]CCTAGCCTCATAAAA | 5607 |
rs530523353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657587 | CCAGTAGCACCGAGA[A/G]CCAAAGTGTAATGTT | 5607 |
rs530539762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622797 | AGTTTAACTTTATAG[C/T]GTTTATAAGAAAGTG | 5607 |
rs530554665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765928 | TTAATAATTAAACAG[C/T]TTCAGTTGTAATGGG | 5607 |
rs530587965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796058 | TATTTGCTATGTTTG[A/G]TTATCCTTTACTTCT | 5607 |
rs530595268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750594 | TCCTGAGCCCAGATC[A/G]CTGAATTAGACTTTC | 5607 |
rs530595495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759357 | TGAGCTCAGGAGTTC[A/G]AGACCAGACCTGGCA | 5607 |
rs530599195 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586282 | ATGGAATACCCTCTC[-/TT]GACATATTTATGCTA | 5607 |
rs530622234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784900 | TCGTGTTTAGCTGAA[C/T]TCGGAGTATGGGCTG | 5607 |
rs530629058 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782972 | AAGTGGGTTAAGCAC[A/C]GAAGGAAGGTGTAAG | 5607 |
rs530635080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758933 | AGACAACTTAGCATT[A/G]CAGACATGCTCAAAG | 5607 |
rs530652400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698389 | GATGGGGGGTTGCGC[C/T]ATGTTGGCCATGCTG | 5607 |
rs530686618 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595710 | ATCACTTTATGTTGG[A/G]GTAATTCCATTTTTC | 5607 |
rs530699261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751448 | CTTATGTAATCAGGT[C/T]CTCCCTAAGTCCCTG | 5607 |
rs530701492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602201 | TCTTCTCTTCCTTAC[A/G]ATCTGACTTAGATTT | 5607 |
rs530718180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742242 | AGAGAATCATTGGAA[A/T]CTCATCATTAGAAGT | 5607 |
rs530721632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595222 | ATATAGGTTATGTGA[C/T]ATAAATATTTATTTC | 5607 |
rs530723589 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587773 | CTGTCTCAGTAAATT[A/C/G]TCCCACATCCAGTCC | 5607 |
rs530733802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795342 | CATAAATTTTCAATA[C/T]TTTTTCCTAATATAT | 5607 |
rs530769432 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622291 | AGAAAGTGGCCCAGC[C/T]CTCAGGAGTAGGTGC | 5607 |
rs530772415 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767866 | TTGAACTTGGCAAGA[A/T]TTTATTTCACTCCCA | 5607 |
rs530794293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636601 | TTTATTAAGAAAGTA[A/G]AGGAATAAGAGAATA | 5607 |
rs530806823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788231 | AATGTATAGCTCTGG[C/G]GCCCCCAGGCCTTCT | 5607 |
rs530807500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648796 | CACTGTGTTAGGATG[C/G]TCTCGATCTCCTGAC | 5607 |
rs530835087 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540668 | TTTAGACAGTATTCA[A/G]TTTGGTAAAGATCAG | 5607 |
rs530842280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606458 | TGTTTTGAAGGTTGA[A/G]TGTATACCATTACTT | 5607 |
rs530855609 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629528 | AGAAAATGATGTTTC[C/T]ATGTTGGCAGTAGTG | 5607 |
rs530857025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643511 | GTGTGCAGTGGCGTG[A/G]TCTCAGCTCACTGGA | 5607 |
rs530883433 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661453 | TAGTGTCAAGGCTTT[C/G]TCAAGTCATCGTTGT | 5607 |
rs530889003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786236 | TTATATGTATGTCGG[A/G]TGTTTGCAATTGGTG | 5607 |
rs530891208 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627903 | TGAGGAAGCTCTTCA[C/T]TGGAGGGCTGAACTT | 5607 |
rs530896319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599708 | TTTTTTCAGGGCTTG[C/T]AGTGGCTTTCCCCAA | 5607 |
rs530904931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555974 | TATTTTTAGTAGATA[C/T]GGGGTTTCACCATGT | 5607 |
rs530941770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641362 | TACTGTAAAAGACAA[C/T]TATGTCGCCATAGAT | 5607 |
rs530947027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749153 | CTGGAAACCTGTATT[C/T]TCACATTTTAATTGA | 5607 |
rs530955836 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793331 | ATGGACATTGTCTAT[A/T]TGCCATGTTCTATAC | 5607 |
rs530960645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598997 | AGTGGCCTATTTGTG[C/T]CCACCAATGGATACT | 5607 |
rs530963783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780448 | AGGCAAAACAGTGTT[A/G]GTTGCACATGCTATT | 5607 |
rs530975353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601535 | GCTGGTTTTCCATGT[A/G]TACACTAATCCTGCA | 5607 |
rs530994106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587260 | TGGGGAAGGGATTTG[A/G]AGAGAGGAGATGAGA | 5607 |
rs530996083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683559 | TTGAGGTCAGGAGTT[C/G]GAGACCAGCTTGGCC | 5607 |
rs531031645 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547716 | CCCACTTCGGCCCCC[C/T]AAAGTGCTGGGATTA | 5607 |
rs531036116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592569 | TCTTTATTTGCTGTG[A/G]ATATTAGTGCTTAGC | 5607 |
rs531038209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697340 | CTCACAACACTATGA[C/T]ATAGGTAATATTATT | 5607 |
rs531049509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786773 | ACAAAAATAGAGTAT[A/C]GCAAAGCATGAAATT | 5607 |
rs531053479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572148 | AAGTTAGGACAAGGG[A/G]ACTAGGAAGGATGTT | 5607 |
rs531057402 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693317 | TAAACTGTAATGCTG[G/T]GCTTGTTTAAACTGG | 5607 |
rs531059801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682657 | GCTAATATGGTGAAA[A/C]CCCATCTCTACTAAA | 5607 |
rs531061233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690583 | CTGATACCCAGGCTA[C/T]AGTGCAGTGGCACCA | 5607 |
rs531069273 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725870 | TTTTCAAAATGTAGG[A/G]CAAACCTACGAACCT | 5607 |
rs531074617 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740807 | CTGAGACAGGCAGAT[C/T]GCTTGAGGCCAAGAG | 5607 |
rs531119913 | in-del | -/TA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701196 | ATTTAGTTATTTCTT[-/TA]ATAATTCTAGAGGAT | 5607 |
rs531124867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780841 | GCCATCCCACCCTGG[A/T]TGTATGGACAGAGCT | 5607 |
rs531132530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675828 | GATTTGATCATAGGC[A/G]GAGTCATCCCTTTTA | 5607 |
rs531141465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627889 | AGAGCCTGAACAGCT[A/G]AGGAAGCTCTTCATT | 5607 |
rs531142440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734352 | ACTTGGCTTGGAAAC[A/G]TGCTATTTTAATGTG | 5607 |
rs531155455 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628216 | GCTGGGTGCAGTGGC[C/G]CATGCCTGTAATCCC | 5607 |
rs531174203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593052 | ATCCATAAGCTTATT[A/T]AACAGATAAAGAGTC | 5607 |
rs531178528 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784554 | ATGGCTGCACACACT[C/T]TCCACCCATCCCCAG | 5607 |
rs531194127 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691986 | CATTAATTTCCTCAT[C/T]GGTTTCATTCAAATA | 5607 |
rs531194188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666238 | TAACTTTGTGCAAGG[A/G]ATCTTAGTAGCACAA | 5607 |
rs531208433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797983 | CCACCATGCCCGGCC[C/T]AAAATGTTTTCTTAC | 5607 |
rs531213743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645075 | ATCGCTTGAGCCCAT[A/G]AGACAGAGGTTGCTT | 5607 |
rs531222227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545652 | ATTATTTCAAGAATA[A/G]CCCAGTGTTTAAGAC | 5607 |
rs531224716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727552 | AGTAACAATTAGATG[C/T]TCCCATTTTACAAGA | 5607 |
rs531229905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720012 | TGTGAGTAGAGCTGT[A/T]GATGGAAATCAACAT | 5607 |
rs531248453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772993 | TGCCTCATCAAGGGT[C/T]ACAAACTTAATGTAG | 5607 |
rs531252490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578932 | TCTATAATTAACTTG[C/T]TAGATAAAGCATAAG | 5607 |
rs531269328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701230 | TAGGATTTTCATGTT[G/T]GTTAGAAGTTCTTGA | 5607 |
rs531288134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638807 | GTGGTTTTGATTTAC[A/G]TTTCTCAAATGATCA | 5607 |
rs531290628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544794 | TAATCAAAATTTGAT[C/T]TCTATAACTTCATTT | 5607 |
rs531295153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544125 | GGCTGGTCTTGAACT[C/T]CTGCGATTTGCTTGC | 5607 |
rs531309099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596813 | TTCCTCCTCCTTCAC[A/G]TCTATTATTCTGCCT | 5607 |
rs531315437 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742738 | AAATTACAATTCTAA[A/G]CCCCTGCTTTCCTTG | 5607 |
rs531317708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597439 | GTTGAACTGGAGTAT[A/G]CTGAAAGACTGAGTT | 5607 |
rs531353062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737078 | GTGGGGGAGAAAGTG[A/G]GATAAGGCATCCAGA | 5607 |
rs531370824 | in-del | -/AGG | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738354 | AAAGTTCCTGGCCAA[-/AGG]CCTCCTTCCAGGCCC | 5607 |
rs531373937 | in-del | -/TTCT | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794283 | GTTAAATACCACAGG[-/TTCT]TTGTGTTTTGTTTTA | 5607 |
rs531374483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603708 | ATAATCATTGATAAA[G/T]GAGGATCCACTTTAC | 5607 |
rs531397001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737762 | TGGAACCAAGTGTGG[A/C]CTGTTAGGCTGCACC | 5607 |
rs531411429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790708 | AGCTGTCAGGAGAGC[C/T]AGTCACATAAAAACA | 5607 |
rs531422206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624700 | AGTGGTGCAATCTCA[A/G]CTCATTGCACCGTCT | 5607 |
rs531425514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552610 | TAGCTAATTAAAAAA[A/T]TTTTTTTGTAGAAAC | 5607 |
rs531446422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783981 | AGAGATTGAAGTAAC[A/C]ATTGCACCTAACTTG | 5607 |
rs531464820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662609 | ACATTTCCTTTTATA[A/G]CAATTTATACATAAA | 5607 |
rs531464859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672987 | AGATATGCGGTGTTA[C/T]TTCTGAGGGCTCTGT | 5607 |
rs531489152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626005 | AGGTGTTGCTTATTC[A/G]AAGTAACAACACTGA | 5607 |
rs531489872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625324 | CAATTTTAAGGGCTG[A/G]GACTGTTCCCAGAAG | 5607 |
rs531510573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576134 | GTTGGCCAGGCTGGT[C/T]TTGAACTCCTGATCT | 5607 |
rs531515470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778088 | GCTAAGGCTTTATGT[A/T]TAAGAGGTGGTAATG | 5607 |
rs531524073 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575939 | TTTTTTTTTTTTTTA[A/G]GATGGAGTCTTGCTG | 5607 |
rs531549769 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746149 | GCAAACTAGAGACTT[C/T]AAGACCTCAGTTCAT | 5607 |
rs531552476 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660624 | GTAGGGAAATAGGTG[C/T]ATATTGAATACTTCC | 5607 |
rs531552748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631483 | TCAAATCACAGATCT[G/T]ACCGTGTCTTGCTGA | 5607 |
rs531554572 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709918 | ACTGAGTATGCTGTA[C/T]AAATACATGTTCTGG | 5607 |
rs531558546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730774 | CCTAAAGTCTAATCA[C/G]GGCACCAGACCTGAG | 5607 |
rs531563130 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577968 | TTGTGCCACTGTACT[C/G]TAGCCTGGGTGACAG | 5607 |
rs531566448 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548958 | ACTATTATGCAAATT[A/G]CCACTGCAGCAAAAG | 5607 |
rs531574113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568439 | GAAGGTAACCACAGA[A/G]GTTTTGTTCAACTCT | 5607 |
rs531583215 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590414 | CTTCCTTCCTCCCTC[C/T]CTCCCTCCCTCCCTC | 5607 |
rs531628466 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793773 | CACGTTGTATATAAA[C/T]GTCCAAGTTTGAAGC | 5607 |
rs531629358 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724403 | TTTATTTATTTATTT[A/T]TTTATTTTTTGAGTT | 5607 |
rs531629422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619044 | TACCTCTCTGACCTC[A/T]TCTCCCCCAGCTAGC | 5607 |
rs531640906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588305 | CCCGTTTTCCTGTTT[C/T]TTTTCATCCCCACCT | 5607 |
rs531658007 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684963 | GATCTTTGAGACACT[A/G]TCAAGAAGTCTAAGA | 5607 |
rs531667171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730107 | ACAGAAGTTGGGGTG[C/T]GTCGTTGCTAGAACC | 5607 |
rs531710880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582398 | TTTGCAGTGACTGGA[C/G]AATTTGGGCAAGTTT | 5607 |
rs531718451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729399 | TTCCAAAGGTTGAGA[A/G]TGTAGCAATATTCTT | 5607 |
rs531720300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721307 | TTTGTGCTACTGTTT[C/G]GGCTCCTTAAGTAAG | 5607 |
rs531725432 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677998 | ATATTTGGATGACCT[A/T]CCCTTTCTTATGTGA | 5607 |
rs531728284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581429 | CCTTGTATCAGATAT[A/G]ATTGTTCAACCGTGT | 5607 |
rs531751304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609712 | ATAGGTCTATAGAAT[A/G]GACTTTGCATATTCT | 5607 |
rs531757815 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623646 | GTTGTCCAGGAGGCT[A/G]GAGTGCAATGGTGTG | 5607 |
rs531772937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574458 | GCGCCTGTAGTATCA[A/G]CTACTCGGGAGGCTG | 5607 |
rs531778217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760707 | AATTAATTTCTTGGT[A/G]GTGGAGGCCTGTGAA | 5607 |
rs531780106 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662551 | AAATTGGTAAGTTCA[C/T]GCTCATGTGCATATA | 5607 |
rs531782657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566385 | TTCTCGATATTGGCC[A/G]GGCTGGTCTCGAACT | 5607 |
rs531808034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617119 | TTTCTCCAAGAGGCA[A/G]AAAAGGGGTATTTCC | 5607 |
rs531816052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623944 | TCTTATCTCATTGGA[C/T]CCTCACAACTCTATA | 5607 |
rs531837934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551832 | TTTGTCTATAATTCA[A/G]AGCATTCAACAGTGA | 5607 |
rs531839305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768336 | ATTGCAGAGGTGCTT[G/T]TATCATCTTCTTTTT | 5607 |
rs531852032 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768120 | CCCCTTAGTTCCTTT[C/T]GATTTAATTGTATTT | 5607 |
rs531856196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644255 | AAAAATCAACCGGGT[A/G]TGGTGGCAGGTGCCT | 5607 |
rs531866166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678721 | CTGTAATCCCAACAC[G/T]TTGGGAAGCCGAGGC | 5607 |
rs531892837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752372 | TTTTGCTAAGGTCAC[C/T]ATCAGGAGTACAAAG | 5607 |
rs531909091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559829 | TTGTTGGTCATATCC[A/G]GTAACGTTTTTTTGG | 5607 |
rs531909581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603158 | TTCACATTGTTGGCA[A/G]CTGTTAACACCATTC | 5607 |
rs531932692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591515 | GCTGGGACTACAGGC[A/G]CCGGCCACCACACCC | 5607 |
rs531952357 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559394 | GTAGGCCATTGTGAC[C/T]GCCCCTTACCTGAGG | 5607 |
rs531952885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797164 | GTTTCTGATCACTCC[C/G]TTCTTACATGTTATC | 5607 |
rs531961215 | in-del | -/ATC | 0.239614 | 0.249784 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612060 | CTCCCTGGAAATTTT[-/ATC]ATCTTTGGTTTTCTT | 5607 |
rs531971030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560367 | GAGTCTTTAATAAAA[C/T]GACTAAGCATAGATA | 5607 |
rs531986468 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700186 | AGTTAACTAAATGTG[G/T]ATTCTTGTCAAGGCT | 5607 |
rs531990447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752264 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 5607 |
rs532009889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708665 | CCTGAAGTGACAGGG[C/T]TCCTCCTTGCCTGCC | 5607 |
rs532018986 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618134 | TACTAGACTCATCTT[G/T]AACATTTCAAGGAGT | 5607 |
rs532019717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804092 | CCTGCAGGCAGAGAC[A/G]CTGCCAGGCTCTGGG | 5607 |
rs532021639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636403 | ACAGAATAAGACTCC[A/G]TCTCAAAAAAAAAAA | 5607 |
rs532042913 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645015 | TAGCCAGGTGTGGTG[A/G]CAGACACCTGTAATC | 5607 |
rs532048235 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588986 | ATCCCTGATTAAGTG[-/T]TTTTTTTTTATTTTT | 5607 |
rs532060034 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646718 | AGATTAAATGCTAGT[C/T]TAATTGGTGGTTTGA | 5607 |
rs532064026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661489 | CCAGCCTACTGAATA[C/T]CAATAATATCCTTTA | 5607 |
rs532069350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804140 | CTCCAGTGCCGTCAC[A/G]ACCCCCCGCCTGCCT | 5607 |
rs532087773 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645287 | GTTCGAGACCAGCCT[A/G]AGCAACATAGTGAAA | 5607 |
rs532101076 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801891 | AAGTTATAGAAAGAG[A/T]TGAAAGTATGGGGAC | 5607 |
rs532102558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804525 | CAGCCCTCTCCCCTC[A/G]CCTACCGGGGCACTT | 5607 |
rs532103740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644141 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 5607 |
rs532112361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603071 | TTGTTATTTTAAATT[A/G]TGGTGAAATACACAT | 5607 |
rs532138160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686480 | GGGGTGGTGGCAGGC[A/G]CCTGTAATCCTGGCT | 5607 |
rs532168299 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733694 | AGACAGGGCTGTCAG[A/G]CCTGTTAGCTGAACA | 5607 |
rs532187348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744642 | GGCTGGTAGCAAGAT[C/T]TGTTTTACCACTTAT | 5607 |
rs532200687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736315 | CACATGCCCCTGAGG[A/G]GTTCCCTGCCACCCT | 5607 |
rs532201373 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686061 | CTAAGAACTAGCCCA[A/G]CTAACCCAAAAGAAA | 5607 |
rs532218632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575287 | GGGGAAATCCTGCAT[A/T]TAAAGGAGAGATGGG | 5607 |
rs532233570 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559693 | AGGCTTTCTGGTTCT[A/G]CTTTTGCTTCCCTAA | 5607 |
rs532250261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596103 | AGCTGCATCTTTTGG[C/T]TGTTATTTTGATAAC | 5607 |
rs532267512 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675657 | AACTTTGAGATAACT[A/G]TGTAAATCTATAGTT | 5607 |
rs532276190 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679844 | TGATATATAATTTGC[A/G]TGCCATAAAATTCAT | 5607 |
rs532276294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752673 | ACAGAGCAAGACACC[C/T]TCTCAAAAAAAAAAA | 5607 |
rs532294726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722906 | CATTCAGCTAGATCA[A/C]TGGCTATATTGAAAA | 5607 |
rs532297781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783693 | AGCCCAGTCTCCAGC[C/T]TGAGTAGAATGCTCA | 5607 |
rs532299291 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642390 | AGAGGCGCATAGCCA[C/T]TCTAATCTTGAGGCT | 5607 |
rs532314340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589684 | CCTGGGCTTTGTTTG[A/G]TTATTTGCATCTTTA | 5607 |
rs532324767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582607 | GGTGGATTGCTTGAG[C/T]TCAAGAGTTTGAGAC | 5607 |
rs532327126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776209 | AGAACCCCACCCCCA[A/C]CCCCACCTCCACTTC | 5607 |
rs532358708 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757084 | TTACTGAATCATAGC[A/G]TAGTTCTTTTTTTAG | 5607 |
rs532363614 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619807 | ATGGCGGTACTCTCC[C/T]GTAGTCTCAACTACT | 5607 |
rs532382157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587679 | AACGTTTTAGTTAAG[C/T]CCTCAGAACGTGGTT | 5607 |
rs532383958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679434 | CAGAGCAGCTACTTG[A/C]GGTTATTGAGGCAAC | 5607 |
rs532386976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734983 | ACTTTTGTCCTCACT[A/G]TTTAGGATATAGACA | 5607 |
rs532391400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596699 | TTTTATGGCCCCTGC[C/G]TCTCTTTCAGCAGGA | 5607 |
rs532411482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594141 | CCTTAAATATCCTAT[A/G]TACAGCTAAGGAGAA | 5607 |
rs532434567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624448 | TAGATTGGCACTGAT[G/T]GCAGAATGCTTCCTT | 5607 |
rs532453981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622993 | TGTAGTCCCAGCTAC[C/T]CGGGAGGCTGAGGTG | 5607 |
rs532455968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629085 | TGAAACCAAGGTGGC[C/T]ATGGCGGTTCCAGTA | 5607 |
rs532466030 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677300 | AAGTAATTTCATTAA[-/T]TTGAACCTCAATTTC | 5607 |
rs532474054 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746319 | GTCATCCCCCTGACT[C/G]TTGGAAATTTGTGAA | 5607 |
rs532478455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729851 | AGAAGAGGCTATTTA[C/T]CTTTGCAGTATGGTT | 5607 |
rs532483643 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630494 | GGCTCTGTACACTGC[C/T]TAACATAGAGCTATA | 5607 |
rs532498409 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781206 | GTTGAAGGTAGCAAA[A/G]TTGTTTTCCTGTGAG | 5607 |
rs532502481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692407 | TTGGTGTGGTGTGCA[A/T]GTGTGCTTTTAAAGA | 5607 |
rs532511692 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684245 | AGCCAAACAATTCCC[A/C]AAACTTATACAAAGT | 5607 |
rs532518390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628832 | GGTCATGGACGAAAC[C/T]TCAGTGGTCATGGTG | 5607 |
rs532524555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781808 | TCTGAATGGCCTGCA[G/T]CTCTTTCTAAATTTG | 5607 |
rs532534784 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580788 | AACAGCAAGTAAATG[A/G]ACAGTTAATAGAGCC | 5607 |
rs532578807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668106 | AGTCAGGTGTTACTA[C/T]TGTTTATTTTGCTCT | 5607 |
rs532584314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581396 | TTTCTTTTTCCCTTT[C/T]AGGTTTGGCAGTACT | 5607 |
rs532588474 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554667 | TCAACCTGCCTTCTG[-/GT]GTGTGTGTGTGCATG | 5607 |
rs532596998 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572912 | CGTATTGGCCAGGCT[A/G/T]GTCTCAAACTCCTGA | 5607 |
rs532603415 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567244 | GTTTGTGTTAATCAA[C/T]AATCTGTTTTTATAG | 5607 |
rs532603971 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715063 | CCATGGAAGATTTTA[C/T]AGGAAAGTGGGGAGG | 5607 |
rs532619912 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751033 | AGCTTAACCTGTTAT[-/G]GCCTGGCAAAGAGTG | 5607 |
rs532621853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651569 | AATCATCACTCTACT[A/G]TGTCTCCATAATCAT | 5607 |
rs532653090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684848 | GAATTAGACACTACA[A/G]AAGAAATTGTGATAT | 5607 |
rs532654646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588158 | AAGAGCCCTTCACAT[A/G]TGGGTGCTCTGTGTA | 5607 |
rs532665510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727758 | ATTCTAAATACAGCT[C/G]TTAATGTAATTACAG | 5607 |
rs532675324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768270 | TATTTACTAATCACA[C/T]AGGAGGCTGTGCAAT | 5607 |
rs532675674 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759732 | CAAGGATGGCCTGTT[C/G]CTGTCACAGCACATA | 5607 |
rs532691343 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781133 | CAGAGACATTCAGCC[A/G]TTTGTGGGAGAAATA | 5607 |
rs532716847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714520 | TTTGCTTTTCTAGCC[C/T]TTGGTGATTGTGAAC | 5607 |
rs532722920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566331 | AGGTGCCCGCCACCA[C/T]GCACGGCTAATTTTT | 5607 |
rs532738535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775367 | ACCAAGAAATTCCTT[A/T]ACTGCTTACATTTTG | 5607 |
rs532765524 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745418 | GCTATAAACTAGGGG[-/C]TTCACTTTTTCATGA | 5607 |
rs532778291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731521 | TTCTAAAGAAAAAAA[A/G]CATGAGGAGCACAGT | 5607 |
rs532791170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660449 | TGGTGTGTAAACTAA[A/G]TATTCCCATAGTCTG | 5607 |
rs532792443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677577 | TTCCTTTGTTTTCTT[C/T]CCTTTTTCCCCAAAA | 5607 |
rs532808662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591128 | AAGGTGGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 5607 |
rs532811883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668557 | TTCAAAACATACATC[A/G]CCACTAATGAGGTGA | 5607 |
rs532840168 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758732 | AAGCCTTAACCTTTG[C/T]GGTTTACACAGTGTT | 5607 |
rs532846596 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620085 | TTAAAAAAAATATAC[A/C/T]AGTAGGCCATGTGCA | 5607 |
rs532853444 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564381 | GAATCAGGGCTCTTG[-/C]TTTTCACTGAGACCC | 5607 |
rs532900871 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643982 | AATGCTACATAACTA[C/T]ACTATCATAGTAATT | 5607 |
rs532904399 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585910 | AAGCCTCCTGGGGAA[C/T]GGAACATACATGGCC | 5607 |
rs532916514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724634 | TTTACCTCCTCCCAA[C/T]AGAACTTGATAAAAA | 5607 |
rs532922041 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577094 | GCGCCCGCCACCGTG[C/G]CCGGCTAATTTTTTG | 5607 |
rs532923773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584887 | ATTTTAGGTAGAGAC[A/G]GCGTTTCACCATATT | 5607 |
rs532932336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633451 | CATTTTGAATTATGT[C/T]TATATAGACTAATAT | 5607 |
rs532933658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693645 | AATGTATAATTCTTG[A/G]ATTAATTCCACAGCT | 5607 |
rs532946863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718876 | GTAAATGGGGTATTC[A/C]CCTCAAGCATTTATC | 5607 |
rs532950610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632831 | CAGATCCTCTGACTG[C/T]TAATGAAATCCAGAG | 5607 |
rs532983808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620480 | CATATAAGGCAATAG[A/G]GTAGTTGATGCCAAT | 5607 |
rs532997573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784743 | GAGGGCAGAGTGTGT[C/T]CTGACAGCTGTCTGG | 5607 |
rs532999570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569191 | AAAGAACAAAGAGGT[G/T]AGAAGCTCATTTTCC | 5607 |
rs533020729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756958 | ATTGACTGATCCTTG[A/G]GTTGTCTTCCTATCT | 5607 |
rs533032289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656441 | GCAATTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 5607 |
rs533054423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711798 | AGAATACAAGCAAGC[A/G]GGCAATCTGATATAT | 5607 |
rs533061945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756403 | CTTTACTGAGGTACA[A/G]TTAACAAATAGAAAG | 5607 |
rs533062777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681654 | ACCTTAAATTAGGAA[A/G]CACCTAAACTTGATA | 5607 |
rs533069383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764769 | AGGTCCCCCTGTCAC[C/T]TTTAATTATGAATTA | 5607 |
rs533070179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779030 | GTCTGGCCACTCATT[C/T]TTGTAAACATCATTT | 5607 |
rs533112505 | snp | C/T | 4.94539e-05 | 0.00497238 | stop-gained, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600703 | AATGAACAAGACATA[C/T]GATATCGGGACACTC | 5607 |
rs533124851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711247 | AAGCAGTTTCAGAAA[A/G]TAAAGATCAGAGTTT | 5607 |
rs533125669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568333 | TTTTGACCTGTGGAG[C/G]ACCTTATAAATTGGG | 5607 |
rs533130921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563419 | TGCTGTTTCTTGGGC[A/G]TAGTGAAGACGAGTA | 5607 |
rs533133299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610589 | AAAAGGCATTTACCG[C/T]GTATAACTTTCTGCC | 5607 |
rs533144761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560662 | GTCCACTTAAGCAAA[C/T]GCTCTTGTAATGTTT | 5607 |
rs533152007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718472 | ATCATTTTTAAAAAA[C/T]TTTTATGGGGGCTGG | 5607 |
rs533152908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661696 | TATCAGAATATATTG[G/T]ATTGCCTTCCCCTAC | 5607 |
rs533172917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716187 | TTTTAGACAAATAAG[C/T]GAGTTAAGCTGCACA | 5607 |
rs533182858 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785241 | TGAGCCACCGTGCCC[A/G]GCCCCGAACTGTTTC | 5607 |
rs533189166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771457 | AAAAAATTAATCAGC[C/T]GTTATTTAAAAGTTT | 5607 |
rs533196274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563889 | CTGAAACGACTTTTC[G/T]TTTGTGTTTAAAATT | 5607 |
rs533200305 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598639 | CTTTTCCCTGTAGTG[C/G]ATGTAAGTGGTAAAA | 5607 |
rs533202540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673905 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCGGC | 5607 |
rs533228784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709566 | AAGTTTGATAGTTTT[A/G]TTAGGGGTGGCTAAA | 5607 |
rs533234490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754085 | GAAATGTCCACAATA[C/G]GGAAGTCTATAGAGA | 5607 |
rs533240983 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624846 | ATGTTGGCCAGGCTG[G/T]TCTTGAACTCCTGAC | 5607 |
rs533243091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703791 | GACTCCAGAAAAATT[A/C]TGTGCCCTGTTGGAA | 5607 |
rs533249918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605834 | TGGAGGTTTTAGTGG[C/G]GCTCTTTCATTGGAT | 5607 |
rs533261008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567643 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGCGCC | 5607 |
rs533272952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570235 | GGTTTTAACCAAATG[C/G]TGTTATCATTAAACT | 5607 |
rs533273542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655540 | TGTTCAAATGTCATT[C/T]CCCTGCCTCTGACCT | 5607 |
rs533301443 | in-del | -/GA | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634880 | CTCTGCTTTTTAAGT[-/GA]GAGTATTGAGACTAT | 5607 |
rs533315716 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773209 | TTGGTCTTTCCTCAG[A/G]AAGAGACAGCTACAA | 5607 |
rs533328392 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629718 | GATGAGAGGAAGAGC[C/T]GTCTGATCTTAGCTA | 5607 |
rs533336300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671566 | TTAAAGTATCAGGGA[C/T]ACTGAAAATGAAGTA | 5607 |
rs533341051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745745 | TCATATAAAGAAAAG[C/T]ACAGTAGCTTTATTT | 5607 |
rs533361922 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661834 | CCCTTCTTCCTCAGA[A/G]TGGAGATGATCACCT | 5607 |
rs533364344 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723461 | ATTTAAGTGTATCCC[A/C]AACTGGTAACACTTC | 5607 |
rs533387752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710203 | CATACGCATTTTGCT[C/T]TTTTCACTTGGATCT | 5607 |
rs533387765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701782 | CTCAGGCAGTTCTGC[A/G]ATGGCTGCTCCAAAA | 5607 |
rs533395210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561419 | TTCTATATCTAAAGC[A/G]AATGAAAGAATCTTT | 5607 |
rs533401561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777138 | AGGGAAGTGTTCACT[C/T]AGCGGGAGAGTGCTT | 5607 |
rs533421556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653920 | TTTTCTATGATAGAA[A/T]TCTCTTGCGATTTCT | 5607 |
rs533453292 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590654 | GATGGGGCCCTACTA[G/T]GTTGCCCAGGCTTGT | 5607 |
rs533453525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598194 | TGGGTGACAGAGTGA[G/T]ACTTCATCTCCAAAA | 5607 |
rs533462042 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611246 | ATATATAGCCAATGA[A/C]ACTTTATAAGTGGTG | 5607 |
rs533476652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762228 | GTAAATGAAATCCCT[A/T]CGGTATGAGACAAGT | 5607 |
rs533485571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639101 | AGACACCAAAAGCGA[C/T]TGCAACAAAAGCAAA | 5607 |
rs533528217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545946 | GCATCTCTAAGTTGT[A/G]CCTGGCTCAAGGCTG | 5607 |
rs533535719 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690142 | CCTAGTTTAGGACAT[C/T]AATATGTAAAAGAAC | 5607 |
rs533536001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799256 | GAAAACTCTGCATTC[A/G]TGGCATTTGCCCAGG | 5607 |
rs533543236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754681 | GGAAATACCTTGATA[C/T]TCACAAAATGAAAGT | 5607 |
rs533556751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646024 | TCTTTGGTCCCATCA[A/G]TCACTTCTGTACCAC | 5607 |
rs533563345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624207 | AGCCAGGCGTGCTGG[C/T]GGGTACCTGTAGTCT | 5607 |
rs533576681 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805471 | CGTGGCGAGGCCATG[C/T]GGCTCTTTAAGCAGC | 5607 |
rs533579425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679324 | CTGCGTGAGGCAGTT[A/G]TGGGTGGCAACATGG | 5607 |
rs533582627 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716588 | ATTTAGAAACTAGAA[-/T]TTTTTTTTAACCTAA | 5607 |
rs533587533 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574214 | TTCCTTGTGAAAGAC[A/G]ATGGTGGTCACTGGA | 5607 |
rs533592654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589827 | TGTGTATAAGAGATA[C/G]ATGGACTTCGAGCAA | 5607 |
rs533607867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604721 | CCAACATAGTGAAAC[C/G]CCGACTCTACTAAAA | 5607 |
rs533613175 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723754 | TTCAGTACACTTTTT[A/T]AAAAAAAAAACTAGA | 5607 |
rs533643205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639627 | ATTTCCCTCTCAAAA[A/G]TCTTCAGAGGCTTCA | 5607 |
rs533662567 | snp | A/T | 5.08264e-05 | 0.00504089 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769715 | AAATGATACATGCCA[A/T]TAACTCGGCAGCTCC | 5607 |
rs533680088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624748 | AATTCTCCTGCCTCA[C/G]CCTCCCGAGTAGCTG | 5607 |
rs533690916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695166 | CTAATGCTAGATGAC[A/G]AGTTAGTGGGTGCAG | 5607 |
rs533700855 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605085 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCAGGCT | 5607 |
rs533715258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653615 | AAAATTTTTTCATTT[A/C]AAATGAAACCGACTT | 5607 |
rs533720378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746309 | AGAGAATGTTGTCAT[C/G]CCCCTGACTCTTGGA | 5607 |
rs533721313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561696 | CACTGAACAGGACTG[C/G]TCCAAGTGCTGGTTT | 5607 |
rs533740362 | in-del | -/TG | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737569 | CATTGAAAAAATCAA[-/TG]AGTTGCCTAAAAGGA | 5607 |
rs533762707 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648133 | CCATGGTTTTTGATA[C/T]ACTCACAAGGTTGTG | 5607 |
rs533763030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619122 | CCTTGGGCTTTTGAA[C/T]TTGCTGTTTCCTCTA | 5607 |
rs533766536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730021 | ATAGAATGTTGTCAC[C/T]AAATTGTTACTTCTA | 5607 |
rs533769841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553803 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 5607 |
rs533789144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671786 | CATTTAGCATTAGGT[A/G]TATCTCCTAATGCTA | 5607 |
rs533789531 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698146 | ATTATAAAAGGGGTC[G/T]GGAAACTTGGAGCTT | 5607 |
rs533814325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754949 | AAATGAGACTGAGGG[A/G]GAAGCTTAGAAGCTA | 5607 |
rs533831473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582758 | CCCAAGAGGTTGAGG[C/T]TACAGTGAGCCATGT | 5607 |
rs533833817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567811 | TGTTGTTCTCATTTC[C/T]TCCTCTCATTTTCTA | 5607 |
rs533840839 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805625 | GAGCGAGGAAGCGGC[C/T]GCTGGACAGGGAGGG | 5607 |
rs533841853 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733269 | TTGATGGCAAGCTTG[A/G]TGTTATTCCAAACGG | 5607 |
rs533848667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654101 | TCTTCTGTATAGTTT[C/T]GTCCATTTTTGAAAG | 5607 |
rs533852010 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773495 | AGCAAATTCCTACCA[A/G]TTTTCTTTCACCTTC | 5607 |
rs533854620 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544767 | TGTGATTTTTCATTG[-/T]CTTGGGTAACTTAAT | 5607 |
rs533856029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568601 | ATAAGGTTTTTGTTT[C/T]GCTCTCTATTATAGT | 5607 |
rs533858425 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605494 | ATGAATCATGATATC[A/T]TATGTATTATCTTAA | 5607 |
rs533863932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618483 | GCTGAGGAAGTCCAG[A/G]TGTATGTCTGTAGCC | 5607 |
rs533888650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609453 | GATTCTGTAGACCTA[C/T]TCTATAGGTCTATAG | 5607 |
rs533892912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670844 | AGAAGTTGCTGTTAT[C/T]ATTGGCACAATTTGA | 5607 |
rs533897197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583608 | ACATAATCGACATGT[A/G]GACATACTGGGTATA | 5607 |
rs533928736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604270 | GCTACATGGAACATA[A/G]AGGAAATACCTTAAA | 5607 |
rs533935264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759947 | GTCCTGTCCTTTCGG[C/T]GATATTGTCAACTAG | 5607 |
rs533940406 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625174 | CTGGTCATCTATAAC[C/T]TATTGTTACAAATGA | 5607 |
rs533949386 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637522 | CTTTTCTTGCCCAGT[A/G]TTAATCTGGAGATCG | 5607 |
rs533955810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714699 | AGTGAAATCTTACTA[A/C]ATGTTGAATATTCCT | 5607 |
rs533988090 | in-del | -/C | 0.00677418 | 0.0578031 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560905 | TTATGTAATCGGTGC[-/C]CCCCCCCTTTTTTTA | 5607 |
rs534013427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699564 | TGCATACGTGTCCTA[A/G]GTTGGACAAGGCACA | 5607 |
rs534021594 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609762 | TGCTCAGGAAGACCT[A/C]TCTGAGGAGGTGCTG | 5607 |
rs534046916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745803 | ATGTTGCATCATCAA[A/G]TTCTTGTGAAATAGA | 5607 |
rs534072758 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725988 | CACACAAAACTTCGA[A/G]AGGGAGTTTGGCAAA | 5607 |
rs534105870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560892 | GATTTAAATGATTTT[C/T]ATGTAATCGGTGCCC | 5607 |
rs534126680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805266 | CCTCGAATGAGAAGG[C/T]TGGGGGCGGGCACTG | 5607 |
rs534146884 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804642 | GCTTGTTCCAGAACA[G/T]ATGATAACAGAGATG | 5607 |
rs534156364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559084 | CCGTGCCTGAGAAGG[A/G]CTTTAAACATGACAT | 5607 |
rs534158236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595657 | TTTAAAAAAAGTTTA[A/T]CACTTAGTCTTTGGA | 5607 |
rs534161675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660097 | TAATTAGGGGTTTTC[C/T]CCCCTAAATATGTGT | 5607 |
rs534168715 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639541 | TCTTGTTCTAAGTGC[C/T]GGTGACCCCCCTGCC | 5607 |
rs534180236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768378 | AAAGCTATTTCCTCT[C/T]GTTCTCAATAATGAA | 5607 |
rs534181243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729688 | AGAATGGCTTGAACC[C/T]GGGAGGTGGAGCTTG | 5607 |
rs534189575 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638342 | GTTTCCTGTTCTTGT[A/G]TTAGTTTGCTAAAGA | 5607 |
rs534193335 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737117 | GTCTAAATGGCCGTC[C/G]TTATTTTACACACAT | 5607 |
rs534211290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616670 | ATAGCCTTTGTTCAC[A/C]GTTTTTCTTGTCTTC | 5607 |
rs534218387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551221 | TCTTATCAACATATA[A/C]AATGTGCAAAACCTT | 5607 |
rs534222821 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796835 | GACAGGAAGTAGGGT[A/G]TCCAGACTGATCTGG | 5607 |
rs534226430 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676607 | GGGTACAATCATAAT[G/T]ATAACAATATTAATC | 5607 |
rs534236625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652638 | CATGAGTTTTGAAGG[A/G]GACAAATATTCAAAC | 5607 |
rs534238137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668195 | ATGTGGCATGTTTTT[A/G]TTATAACCATGAATT | 5607 |
rs534240561 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673657 | ACAAAAGAATTCTTG[G/T]AAAGTATTGCTATCA | 5607 |
rs534242833 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631754 | CTCTGCCACTGCTGG[C/T]GCTTGATCTTCCCAT | 5607 |
rs534267318 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752417 | GGGCACGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 5607 |
rs534291064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555458 | ACTTTGGAGGGGACA[A/G]ATATTCAAACCATAT | 5607 |
rs534297681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707953 | TCTCCTAGGGTACCT[A/G]TGGTAAAGAAAAAAA | 5607 |
rs534304655 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705579 | GTCTCAACTAAAAAT[A/G]CAAACAATTAGCTGG | 5607 |
rs534307953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760845 | TTTAATCCACCATGA[C/T]GGGACCTACACACCC | 5607 |
rs534310188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566396 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAA | 5607 |
rs534319938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711367 | ACCAAGGTATCAGAT[C/G]CAGATTTGAATTCCA | 5607 |
rs534321185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803663 | CCCTGAATCCCATGC[A/G]GGGCTGATGGGAGGA | 5607 |
rs534351965 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751241 | AAACTCAGACCACAG[A/C]TCAGGACCTGGGAGG | 5607 |
rs534352609 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564691 | TGAAAGGCAGAGTAG[A/G]ATTGTCTGCTGAAAA | 5607 |
rs534361628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544233 | TGTAAGACATTTTAC[C/T]TAGAAAAAAATGCTA | 5607 |
rs534363535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664775 | CTCAAAAAGATGGCT[C/G]CTCTATAAATGTTAT | 5607 |
rs534392059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644326 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 5607 |
rs534400564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797548 | TCTCCTGACTGCCAA[A/G]TTGCTACCCTTTCTA | 5607 |
rs534405082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606719 | TGGGAGCTGGAATCA[C/T]ATTAGCTCATTATAG | 5607 |
rs534408646 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599177 | CACCTTTTATACAGC[G/T]TAAAATATTTTTTTT | 5607 |
rs534422325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757297 | ATAAAAATAGTATTT[C/T]TAGAAGACATTTGCA | 5607 |
rs534426393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563648 | CAGTACTTAAAGTAA[C/T]GGCTCATTAAAAATG | 5607 |
rs534436827 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561854 | AGGGGGATATCCTTG[G/T]AACTACAGCCAGACA | 5607 |
rs534439959 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555354 | AGTGAGAACCCACTA[C/T]CATAGAGAGGGCACT | 5607 |
rs534444761 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579836 | GATTTCCTAAACATA[C/T]CGTATTTAAATAATA | 5607 |
rs534472109 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589516 | GGATGATTAAACTTT[C/T]CATCTATCTACTGCT | 5607 |
rs534485582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592741 | CTAACAGGGTTTTAG[G/T]CTCTTTATTTGATAC | 5607 |
rs534486321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686230 | AAAGAACAAGACACA[A/G]CTGTACAGTGTTTGC | 5607 |
rs534488368 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693969 | GTCACCAGATCAAAA[A/T]TAAATTACTGTGTAG | 5607 |
rs534490113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741130 | TAAGCCCGTCAATCC[A/G]AGGTCTGTGTTCAGG | 5607 |
rs534492636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551884 | TTTTTACATTTGTAC[A/G]GAAAGATATCTGTGA | 5607 |
rs534493414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790291 | TGCCCCTAGCCCTAA[C/T]GTGCCATTAATGATA | 5607 |
rs534499271 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768643 | GGGAGGAAAAAAGCC[A/G]CCGAAAGGTATTTTT | 5607 |
rs534508110 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641628 | TTATTTGTCCTGGAG[G/T]TGTAGTGGAGAGCAG | 5607 |
rs534509787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589382 | TTAGGTGAATAACTG[C/T]TTATTAAACTGGGTT | 5607 |
rs534520048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583332 | TGGGGAGAGGATACT[A/T]AAAGGAGGAAATTAT | 5607 |
rs534560277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734516 | GAGCACTTTTCAAAT[A/G]CTAATGTTGAAGTAC | 5607 |
rs534563100 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616829 | TTTTAGTGACTGGAT[A/T]ATTTTCTTAGGTTTC | 5607 |
rs534577573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628017 | AAGTGCTCCTGGGGC[C/T]TTGGGTTTGTCACAT | 5607 |
rs534580920 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655839 | TCTCTTTCTGATCTC[C/G]CATTAAGCATATGTC | 5607 |
rs534624745 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553186 | TACCTGTGAGGAAAC[A/G]AAGCTTAGAGGCCTG | 5607 |
rs534629776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806388 | CCTTCCAGGCTAGTG[A/C]GAGCCTCAGGAAGAG | 5607 |
rs534639763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764058 | TGGTGGCTTGACACC[A/G]TAAGTCTAGAAGTGG | 5607 |
rs534643091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733937 | TACATATCAAAGTAT[C/G]AGAGGAGCTGTAGGT | 5607 |
rs534650313 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804752 | CACTCGTGAGCACAG[C/T]TTCTCCCTTTGTTCT | 5607 |
rs534658698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546761 | TCCAAGCTCAGATTT[C/G]CCCTCATCTATAAGA | 5607 |
rs534663671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695429 | TTTATACTTTCTTGT[A/G]TAATAATAGGAAAAA | 5607 |
rs534669091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791619 | GCACAGGTTTGGGAG[C/T]TGACATCCAGTGCAA | 5607 |
rs534693328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584652 | CTGCAGTGTTTTGTA[A/G]TTATTACCCATATCT | 5607 |
rs534696256 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779858 | TTCAGTGCCGTGCCA[G/T]ATTTGCGGCAGCGGG | 5607 |
rs534703301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799392 | CCTCACCTGCCCAGA[A/G]TATATCTGTGAAGCA | 5607 |
rs534710312 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636543 | GGTTGTATTTTTCAC[-/T]TTTTTTTTCATATCT | 5607 |
rs534721276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656626 | GAGCCATCGTGCCTG[A/G]CCACCTTTTAAATCT | 5607 |
rs534738576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800352 | GTATCCATTGTAGAC[A/G]CTTCTTTTTAAAGTC | 5607 |
rs534782724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794236 | TTTCTTCAACATTAC[C/T]TTGGAAACCACAGTA | 5607 |
rs534784204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688439 | ATTGTTGAGGAAGGG[G/T]TGCATATAGTCTGGC | 5607 |
rs534811119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591322 | TGCACTCCAGCCTGG[A/G]TGACAAAGCGAGACT | 5607 |
rs534820713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793436 | TTGTTGTATAGTTTT[G/T]CTAGTAGATGTCATT | 5607 |
rs534834309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639770 | TTTTAAGTTGAACTC[A/G]TTGCCTTATCTGAAC | 5607 |
rs534854207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681891 | ACTAATTGATAAACC[C/G]TAATAATTAATGCCC | 5607 |
rs534856840 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742486 | GTAGTCTAAAGGACC[A/G]TTCTCAGAAAAAGCA | 5607 |
rs534867249 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779244 | AAGGCCATTAAAATC[A/G]TCTGTTTGTGTCTGC | 5607 |
rs534867972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726473 | TAAATCCAAGATAAG[A/G]TGCATACTAATAAAA | 5607 |
rs534868306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651328 | AGTAATCAACTCAAA[A/G]TAATGGAGATATGTA | 5607 |
rs534891207 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635319 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC | 5607 |
rs534900009 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799932 | CTTGCTGTCACTCCA[C/T]GCAGAGTGGGGGGCG | 5607 |
rs534902706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690797 | CCTCAGCCTCCCAAA[G/T]TGTTGGGATTACATG | 5607 |
rs534903646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780025 | GTCCTCCTCCCTGCG[A/G]CTTTTCCCTACTCTT | 5607 |
rs534912026 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621019 | TAGGTTGCATTTTTT[A/T]AAATACAGTTATGTG | 5607 |
rs534922723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732837 | GTTCCTGGTGCATCT[G/T]TCTGCGCCAGGCTTT | 5607 |
rs534942021 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684539 | AAGATTCACAATGTT[C/G]ACAATCCAAATAAAA | 5607 |
rs534948806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585108 | AAATCAAATTAATTC[A/G]TCCCCAAACAATCAA | 5607 |
rs534956925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785479 | GGAATACAGAGGGCT[A/T]TCAGACACTAATCCA | 5607 |
rs534985614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598392 | TATGAGACTCTTGCA[A/G]TCCTCCTGGTTATCT | 5607 |
rs534986021 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720194 | GTTACTCAGCTAGGG[-/T]TTTTGGTTTAATGTA | 5607 |
rs534992867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620833 | AACTAAAACAGTGAA[A/T]AGAATGTGTAACTTC | 5607 |
rs534996253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746511 | CATAGGAGAGGTTAT[C/T]CAGGCTTTTCAGTAT | 5607 |
rs534997804 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738122 | CTCCCAGAGTACTGG[A/G]ATTACAGGCGTGAGC | 5607 |
rs535007368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674177 | AAAGAACTGGTTAGT[G/T]CTTGAGTAACCCAAG | 5607 |
rs535007610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639288 | CCAGATGCTTGGCTT[C/T]TTTCTTGTCAGACAT | 5607 |
rs535012551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718124 | TACAGAGGCCAGAAG[C/T]ATGAGAATATCAGCT | 5607 |
rs535030809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695024 | ACAAAAAACCAAACA[C/T]CACATATTCTCACTC | 5607 |
rs535040281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612736 | AAAAGCCATTTCTTT[A/G]CAGAATGGTAGCTGC | 5607 |
rs535040372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587242 | CAGGGAGGGGTGCTG[A/G]GTTGGGGAAGGGATT | 5607 |
rs535055023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713215 | GATTAGTAATAGAAA[C/T]TTTCCCAAGGAAAAT | 5607 |
rs535066313 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596903 | TTGGCCGGGCATGGT[A/G]GCTCACGCCTGTAAT | 5607 |
rs535072023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731860 | TTCTTCTAGTTTGCC[C/G]TCTCTGCCCTAGGGA | 5607 |
rs535098928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612095 | TTTTTTTTTTTTCAC[C/T]GCCATGATTTTGTGA | 5607 |
rs535100692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717901 | CAGGATTGTTCCTGC[C/T]ACATTCTGTTGATCA | 5607 |
rs535106000 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593528 | GTTATTTCTTACTAA[A/T]TTTGATTCAAGTAAA | 5607 |
rs535125696 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798669 | AGGTGCCTGCGTACT[A/C/G]TCTAGGATGGCTAGA | 5607 |
rs535158443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632161 | CTGGAGTGCAGTGGC[A/G]TGATCTAGGCTCACT | 5607 |
rs535163248 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786866 | ATGGTAACCATTTTT[A/G/T]TCGTCATTGTCATCA | 5607 |
rs535165982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738858 | ATGAGCAGCTTCCTC[C/T]TCCTGTCCACACCTT | 5607 |
rs535166597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605458 | ATACTTCTGTATTTT[C/T]TTCTATTCTGTAGTT | 5607 |
rs535193751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711319 | TGGAGAATAGATCAC[A/C]GTGTTGTGCTTGTGA | 5607 |
rs535235066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724890 | CACTCTGTAAGAGAG[A/G]AAGTGATTGTCATCA | 5607 |
rs535261536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599072 | CTCTGCTAGTTTAGC[A/G]TCTCGTCACTTTATG | 5607 |
rs535263395 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647158 | AACACAACTTAAGAA[A/G]ATATTGTTAGTTCCT | 5607 |
rs535263620 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547892 | TACCCTGCTTTAAAA[C/T]GACTAGTAGATATTA | 5607 |
rs535293530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605874 | ATCTAGCTACTTTGC[A/G]AGGCTGTACAATTGT | 5607 |
rs535297637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746850 | TTAAAACACTCAGGC[A/G]GTAGGAAGAAGGGTG | 5607 |
rs535297998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703923 | TCATTCCAGTATAGT[C/T]TTATCACATGTGTAT | 5607 |
rs535312728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612807 | GTTGATGAAACTGTT[C/G]AATTAAAGCACAGGC | 5607 |
rs535313062 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770182 | CTATGAAAACAGTTC[A/C]GCCCACTTTAACCCT | 5607 |
rs535330545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634018 | TTTAAATTTGTTGAG[A/G]CTTATATTATGGCTC | 5607 |
rs535331305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663911 | TCATAAGTGTCATGA[A/C]TTCAAAAAAAGTTTT | 5607 |
rs535337066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641473 | ACTCCAGCAAATAAA[C/T]GAAGTCATCCATGAC | 5607 |
rs535361611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771622 | CAACTCCACTGGCGA[C/G]ACAGCTTGAATTAGT | 5607 |
rs535364647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723441 | GATGTTAGTTGTTTA[C/T]TGCTATTTAAGTGTA | 5607 |
rs535370739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785478 | GGGAATACAGAGGGC[A/T]ATCAGACACTAATCC | 5607 |
rs535373101 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643947 | TCTTCAGTTGTAATA[-/C]AAAATGTAATTCAAA | 5607 |
rs535375687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620185 | AGACCAGCTTGACCA[A/G]CATGGTCAAATGCCA | 5607 |
rs535384688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763243 | CTGCATCATGAAATC[A/G]AAAATAAACTTAGAG | 5607 |
rs535389920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627104 | CAGGCACGCACCACG[A/T]TGCCAGGTAATTATT | 5607 |
rs535395237 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640806 | GGAATATATTACAAG[A/G]TATTTTTAAAAGAAG | 5607 |
rs535403390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556075 | ACAGGCATGAGCCAC[C/T]GTACCTGGCCAGCTA | 5607 |
rs535414555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694268 | AAAAAAAATTAAACA[A/G]GAAACTTATCTAGTA | 5607 |
rs535426418 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553730 | CATCCTGGCTAACAA[A/G]GTGAAACCCCGTCTC | 5607 |
rs535429143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663834 | GTGCTATGATTGCAC[C/T]ACTGCACTCCAGCCT | 5607 |
rs535436754 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706553 | AAGGAGCCGGGTGTT[-/A]ACAGCAGGAGGAAGA | 5607 |
rs535463640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701398 | TAGGTATGTCTGCCT[A/C]GTACTCTCTTTGCCT | 5607 |
rs535467829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805131 | AGCGGGTCCCTGCCC[A/G]GGGTTGAGTGCCTTG | 5607 |
rs535476440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771090 | CAGAAATGTATATCC[C/T]TCTTAATTTCCTTTA | 5607 |
rs535481062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563540 | AGACACTTACTGATC[A/T]TATCATAAACATTAA | 5607 |
rs535484984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554848 | ATTATAAAATGTATA[C/T]GGTCTAAATCTAAAT | 5607 |
rs535486323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568819 | TGACCATCCTGACTA[A/C]CACTGTGAAACCCCA | 5607 |
rs535486887 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659841 | AAGCATGTTCTTCCT[C/G]AACTTCATAAATCTT | 5607 |
rs535491015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662727 | ACATCTTTTTTTCAG[C/T]ATCTCATTCAACTAA | 5607 |
rs535491853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798343 | CCAGAGCAGCCACCA[C/T]AGCCCCCTTTAAACA | 5607 |
rs535497496 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694517 | GAAAAAATGCTCATC[A/G]TCACTGGCCACCAGA | 5607 |
rs535499422 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655884 | TATTTTACAGGTCTC[C/T]GAGAATGTGTTCATT | 5607 |
rs535507871 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545990 | GAAACACGAGTGGCC[C/G]CACCACTAGAGCTCA | 5607 |
rs535512320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699102 | AGTTATTTAGATCAA[C/T]TCTTCTGTTTAAATA | 5607 |
rs535543770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806362 | CGAAGACAGGCCCTC[A/G]CCCTTAAGCACCTTC | 5607 |
rs535548746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694904 | AAAAATGTGGCACAT[A/G]TACACCATGGAATAC | 5607 |
rs535554891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590083 | TTCTACAAAATTGTT[A/C]ATTGCCACTTTAGTG | 5607 |
rs535564214 | snp | C/T | 0.000248544 | 0.011145 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692428 | CTTTTAAAGAACAAA[C/T]GCTGTAGATACATGG | 5607 |
rs535611795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576777 | AATGCTGCAACACTT[C/G]TAAGATAGAAAGTTT | 5607 |
rs535655841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800235 | GGGATTAGATTGGTA[A/G]CTTTAAAACTTTAAC | 5607 |
rs535688458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590706 | CGATCCTCCTTCCTT[A/G]GCATCCCAAAGTGCT | 5607 |
rs535708495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724786 | CTCTCCTGGGGCCTT[A/G]AAATGACTGCTTTCA | 5607 |
rs535722775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785760 | CAGGATGTGTTGTGC[A/G]TAAAGCCTGGAGAGG | 5607 |
rs535746363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740213 | TCCTAGAGTCTAGTA[C/T]AGCGCCTGGCATAGC | 5607 |
rs535749412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555384 | TGAGTCATTCATGGG[A/G]GATCCACCCCCACGA | 5607 |
rs535761009 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541407 | AAGTAAAGCCAATTC[A/G]TGCACCTTCATAAGA | 5607 |
rs535770763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584284 | AAGTTTGAGAAGTCA[A/G]TTGAGGAGTGAGGCA | 5607 |
rs535804651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597117 | GAGCTTGCAGTGAGC[C/T]GAGATCACGTCACTG | 5607 |
rs535819933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795482 | TTAGGACTTTTTTAC[A/G]CCAAATTATTTAGAA | 5607 |
rs535819973 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769318 | TAATTTCTCATTTAC[A/C]CTTTCCCTACCTTCT | 5607 |
rs535822133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731642 | CCTGACTCAGGCTGT[G/T]CATTCTACCTGCAGG | 5607 |
rs535832257 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586494 | GTTGCAGAGCTGGAA[A/G]GATATAACTTGAGGT | 5607 |
rs535895864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600930 | AGTGCATTTATATTG[A/C]CTTTTTAATATTTCC | 5607 |
rs535917507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738067 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCCGAC | 5607 |
rs535924586 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797318 | TGATTGTATTCCTTC[A/G]GAGGTTTCTTTTCCT | 5607 |
rs535924925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639221 | AAAATTTTGCGAACT[A/G]TGCATCTGACAGAGT | 5607 |
rs535926022 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662285 | TGCATTTCTTATTTC[A/G]CAGTTGCTCTTAGGC | 5607 |
rs535932898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691962 | AAAACATGTGAAATA[A/G]CAGTACTACATTAAT | 5607 |
rs535946839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549831 | ATGTGGAAAAGTTTC[C/T]TTAAATATTTTTCTT | 5607 |
rs535951049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553160 | ACTGAGTCTGTGAAA[C/T]AGGAAAATTATACCT | 5607 |
rs535964230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745794 | ATTACAATGATGTTG[C/T]ATCATCAAATTCTTG | 5607 |
rs535970492 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758388 | GGCACACGGAAAGAG[-/A]GGCATTTTCAAGGGA | 5607 |
rs535971588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798759 | ATTATGAAGAATAAA[C/T]TCAGGAAGGTTGATT | 5607 |
rs536008582 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636951 | TGGCTAGGATAAAAG[C/G]AGGCAGAAGTTGGAA | 5607 |
rs536009416 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799940 | CACTCCACGCAGAGT[C/G]GGGGGCGGTGGGGGG | 5607 |
rs536028092 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677045 | GGGAATAGTTAGAAC[G/T]TTCCTCACACTTTCC | 5607 |
rs536043962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573060 | TATTAGGGTATCAGG[A/C]CATTCCTGAACCTGG | 5607 |
rs536044251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728069 | TTAAATTGAAAAGTG[A/G]TATCTTAAAGGGTTC | 5607 |
rs536081347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587858 | TCAGTGCCACACCCT[A/G]TCAGTCCCCACACTT | 5607 |
rs536087296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673143 | TTGACTTGGCAATGC[A/G]GTCTCTTTTTTGGTT | 5607 |
rs536088030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684461 | AGTGTTCAGCAGATA[A/T]ATTACTTGCCAGTAT | 5607 |
rs536099732 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669196 | AATATGTGAAACAAA[A/G]GATTTCTATGATCAT | 5607 |
rs536103974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714052 | ATATTTATTGAACAC[C/G]TTTTACATGTCAAAC | 5607 |
rs536106510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565985 | TGGACGTAACCTTAC[A/G]GTAGGTTTTGATTGG | 5607 |
rs536126191 | in-del | -/TAAA | 0.0170251 | 0.090679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644393 | GCAGGACTCCATCTC[-/TAAA]TAAATAAATAAATAA | 5607 |
rs536126484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619198 | CTGCTCACATGTAAC[C/T]TGAAAAGAGAGGCAT | 5607 |
rs536133210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615821 | TAATCTCGCAAGGTA[C/G]TAAAAGATTTTTGTT | 5607 |
rs536133713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778465 | AAGACAAAATGCACT[C/G]GACAATTAAGAAGAT | 5607 |
rs536164406 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672115 | GTGAATAGTGCTGCA[A/G]TAAACATATGTGTGC | 5607 |
rs536186295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625683 | TCATGCCTGGCATTG[C/T]CTTTGTCATCCAGTT | 5607 |
rs536193009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623096 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAG | 5607 |
rs536199783 | snp | C/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719731 | CTATCTACTCATCTG[C/T]TGCAACATCTCAGAT | 5607 |
rs536208384 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601660 | TCTAATTGGTTACCC[A/T]TGTTCTTAGAATTTT | 5607 |
rs536219309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682847 | CAAAAAATAAAAAAA[A/G]AAGAGTTGTAGGCTG | 5607 |
rs536244695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650920 | GTTAATTCTTTTTTT[A/T]AAACATTTTAGGGGC | 5607 |
rs536247920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750777 | ATCTGACTTTTAGAC[C/T]TTTTATTTGTGAATG | 5607 |
rs536250325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634759 | TTGACAAGTGTTAGC[A/G]TGATATTTTTTTTTT | 5607 |
rs536252913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706318 | AAACTATTGAATATT[A/C]TGTGGAGGACTGAAG | 5607 |
rs536255300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794461 | AAACATTGGTCGCTA[A/G]TAGCAGAAACTTGAG | 5607 |
rs536273581 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542582 | TTCCCACGCCGGGGG[A/C]GCATCCTCCCGGGAG | 5607 |
rs536287558 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583622 | TAGACATACTGGGTA[G/T]ATTTCCTGTGTCTAC | 5607 |
rs536293443 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779371 | ACTAAATCAGACAGC[G/T]TTAATTTGAATTTTT | 5607 |
rs536296331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786377 | TATTATTGGTAAAAT[G/T]TAATGAGCATCTTGT | 5607 |
rs536298527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571496 | CCAGATATCTCAGTC[A/G]CCTTGTTTTATGGTT | 5607 |
rs536307540 | in-del | -/ACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697812 | TATGTGAATAATCTC[-/ACTT]AATCTGTAATCGAAA | 5607 |
rs536325188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621389 | TGGGACAGGGAATAA[A/T]CCCAAAGAAAGTGGA | 5607 |
rs536349471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594371 | TGTATCTTCAACATG[C/G]TTGCATTCTAGTTAC | 5607 |
rs536355724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734655 | TTAGACCACAGATAT[A/C]ATTATCTTATTTATG | 5607 |
rs536369389 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711255 | TCAGAAAATAAAGAT[C/T]AGAGTTTAAAGTGTG | 5607 |
rs536382505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642885 | GTGGCTAGCAATGTG[A/G]AATCATGTCATTTCT | 5607 |
rs536383954 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556676 | TCTGCCTCAGCCTCC[C/G]TAGTAGCTGGGATTA | 5607 |
rs536394356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771483 | AGTTTTATGGAGACA[C/G]AGGGAGGGATAACCT | 5607 |
rs536419806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556419 | TATTCTTTTTTCCTT[C/G]TACTTTAATGAGGTT | 5607 |
rs536451590 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628902 | GTGGGGATGGATGGC[G/T]ATAATGGATTTAGTA | 5607 |
rs536490313 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773069 | GGATTGGTAACAGAA[G/T]ATCATCAGTGCAATA | 5607 |
rs536495898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573973 | CTTGCTTTTGGGAAC[A/G]CCCAGCTCTGACTGG | 5607 |
rs536505743 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650306 | TTCAATTCTGAATGT[A/C/T]TTTTATTTCCTTTTC | 5607 |
rs536542067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705781 | CTAGTCCTCTCTGGT[A/G]AAGTACCACTTGAGC | 5607 |
rs536545951 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801969 | AGGGCAGACAGCGAG[C/G]TGTCATTAAATGAGC | 5607 |
rs536551598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667698 | GGGCACAAATTTCAA[A/T]AGATTAAGAAATGGA | 5607 |
rs536569382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766859 | TTGCCCAGTGTTTAT[G/T]TGTGGCATTCTCACC | 5607 |
rs536571934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774920 | AAATCAAAGAAAGAA[A/T]ATTAGAGATGGGCAG | 5607 |
rs536576622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713148 | AATCATTTTTTTTCC[C/T]CAAATGACATATGGC | 5607 |
rs536578572 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807560 | GTAAGCCTGGCTACC[C/T]CCATTTTGCAGGTGA | 5607 |
rs536589480 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696035 | TGTAAGGTTGGGGGT[C/G]GGGGGAGGTGGAAAT | 5607 |
rs536589919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629233 | CTCAGCCAAGCACGG[G/T]GGTGGCAGGGCCTAG | 5607 |
rs536594318 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728775 | TTATGCAAATAAGTG[A/T]TGTATTACACATACT | 5607 |
rs536599450 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575424 | AAGAGCCAGAGGTCA[-/C]CTAGGTCACCCATCA | 5607 |
rs536605281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600141 | TGATTTCTGCCTAAT[A/T]ATTGCTGTATACTAG | 5607 |
rs536606829 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696993 | TCAAAAAGAAAAAAG[A/G]AAAGAAAATGAGACT | 5607 |
rs536607405 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548974 | CCACTGCAGCAAAAG[C/T]TTCTAAAGAATTGCC | 5607 |
rs536614554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674429 | ATTAATCACATCCAG[C/T]GCTATAGTAGATTAT | 5607 |
rs536635116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725654 | GTTATTAAGCTATTA[G/T]CTTTTTTAGGTGTGA | 5607 |
rs536635321 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579122 | ACAGCCACTGATTGG[A/G]AAGTTGCTTGCAGCC | 5607 |
rs536651784 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643100 | GGGGTAAAGCCTGCA[C/G]CTTGGGATTTTTTTC | 5607 |
rs536652909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627392 | CTTGCTTTTTCTTTA[A/G]ATGAAATATACTTGA | 5607 |
rs536653545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705216 | TTAGAGCACATATAA[A/G]TGTTCACTATTCATC | 5607 |
rs536662749 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807415 | ATCCACCTGACCTGC[A/G]TGGCTGAGGAGGGAG | 5607 |
rs536670587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606831 | ATGCTATTTAGTAAA[C/T]AGAATATTTCAAAAC | 5607 |
rs536684239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586493 | GGTTGCAGAGCTGGA[A/G]GGATATAACTTGAGG | 5607 |
rs536704999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719317 | GTTCATTAAGGTACT[C/G]TGGCATAGAAACAAG | 5607 |
rs536719704 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741904 | AGAAAGAACTTTTTT[C/T]TTTTTTTTGAGAGGG | 5607 |
rs536735114 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639775 | AGTTGAACTCGTTGC[C/T]TTATCTGAACTCAGG | 5607 |
rs536743568 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540747 | GATTATGATGCTTCT[C/T]GCAATGAGAGTTATA | 5607 |
rs536760274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749839 | ATCCTCCCAATTTAA[C/G]TGGTTTTCCTGAGGT | 5607 |
rs536789868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621018 | TTAGGTTGCATTTTT[A/T]AAAATACAGTTATGT | 5607 |
rs536793000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726330 | TTTGATAACTTCAGC[A/G]TATTCATGTCTAAGC | 5607 |
rs536798693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607052 | ATTTTTGCATGATGT[A/G]TATCTTGTAAATTAA | 5607 |
rs536798805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614942 | TGAAATTAATATCTG[G/T]GACCTCATAACATAT | 5607 |
rs536808380 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757170 | TCCCATGAACAGTGT[A/G]TAAGGGTTCCCTTTT | 5607 |
rs536815966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683715 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTTTA | 5607 |
rs536823624 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587433 | CTGTGTTTTTAAAAG[A/G]TCCTCTGCCTGTGGT | 5607 |
rs536832285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565215 | TTGCAGGATTTTTTT[A/T]ATGTCATCACTGTTA | 5607 |
rs536870252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622232 | AGTCAAAGAAACAAT[A/G]TAGGACCTGAAGGAA | 5607 |
rs536880951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593429 | TTCCTGGCCTTCAGG[A/T]GACCTTAGTTTGCCT | 5607 |
rs536887249 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562452 | TTTGAATAAGAGAAG[C/T]ATCATGAAATAAATA | 5607 |
rs536889916 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592207 | ACACTTTAATACTTC[C/T]TAAATAACTCTGGGA | 5607 |
rs536897120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675956 | AAGGAACAAATGCAA[A/G]TGGAAGAGGATAGTT | 5607 |
rs536899247 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594822 | ATTCCCTCAAAAACC[-/A]AAAAAAACCCACCTT | 5607 |
rs536927269 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619454 | GCAATCAGAGACATG[C/T]ATTAAGTATTAAATA | 5607 |
rs536966975 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558435 | TGGCCTCCAAACTGG[G/T]CTCCCTGTTCTACTT | 5607 |
rs536986526 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791074 | CACCTGTGAGACATC[C/T]GAGCTGCAGCTGGGC | 5607 |
rs536988038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628466 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTAAA | 5607 |
rs537010106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785627 | AGATGTCCACACCAA[C/T]ACAGGTGCTGGAGGT | 5607 |
rs537022006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681494 | CTATTTTGATGCCTA[G/T]AAAAGCCTACTGCAT | 5607 |
rs537023672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689331 | AAATGGTACAGACAG[A/G]TGCTACAGAAATTCA | 5607 |
rs537027778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739895 | GGTAAAAAAATGTTC[A/G]GTGATATGTGGAACC | 5607 |
rs537040614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640705 | TTTCCTACTCAAAAT[A/G]TTTCTCATGTTATGC | 5607 |
rs537048543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785003 | GGAGTGCAGTGACAC[C/G]ATCTTGGCTCAGTGC | 5607 |
rs537054617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792530 | TTAAACCAGCTGACA[C/T]TCACTCTCTGACCGT | 5607 |
rs537062231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801165 | ATCACAGCCAAGCGG[G/T]CTGGAATCCTAAAGG | 5607 |
rs537071784 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540954 | GGTTTTCCCCACGGT[A/G]CTTCGAATAAAAGAG | 5607 |
rs537079833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757402 | TGCTCAAAAACCCAA[C/T]CTATAAAATAGATGA | 5607 |
rs537086264 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685302 | TAATGGAAAGACGTC[C/T]TTAAAATGTTGAAAG | 5607 |
rs537113865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642278 | GTAAAGACTTGAGTT[A/G]AATCCTACATCACTT | 5607 |
rs537119792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627202 | GATCCTCCTGCGTTG[G/T]CTTCCCAAAGTGCTG | 5607 |
rs537133869 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802973 | AAGGCGTTTGGAGTC[A/G]GAGACCCATGTTCTG | 5607 |
rs537142718 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753981 | TGGACTATAAATAGG[A/G]ATGAAGTACTGATAA | 5607 |
rs537150158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600814 | AGTATCCAAGTTCTC[C/T]GTGGCAAAGATTTTT | 5607 |
rs537155221 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751595 | CTGAAATTTATGACT[C/G]TAAGCTCTGACAGCT | 5607 |
rs537157987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586253 | GATTAATTAAGCACA[G/T]AAGCATATTGCACAT | 5607 |
rs537175328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650200 | TTGCTGAACTTGTTT[A/T]CTAATGTTAATAGCT | 5607 |
rs537180572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633906 | AGAAGTGTGTTATTT[A/T]GTTTCCAAATATTTG | 5607 |
rs537201196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772257 | GTGAAAGAATGAGAT[A/G]TATTCTCATTTGACT | 5607 |
rs537226371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571448 | ACTGACTCAACCTCA[A/G]TAAACCAGTTAAATT | 5607 |
rs537251162 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623616 | TTTTTTTTTTTTAGA[C/T]GGAGTTTTGCTCTTG | 5607 |
rs537263103 | in-del | -/A | 0.252983 | 0.249982 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682677 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG | 5607 |
rs537283948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779775 | ACAGTGAAGCTGTGT[A/G]GCATTCATTGAGCAC | 5607 |
rs537294314 | in-del | -/CTCTTAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655196 | CAAATTTAAAATTAT[-/CTCTTAA]GCCATTGTCTCTTAA | 5607 |
rs537300040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578198 | AGCTCCTGGGTTTGA[A/G]CCCTCTGATTCATTC | 5607 |
rs537300433 | snp | A/G | 1.96338e-05 | 0.00313313 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806872 | GGCTTCCCTGCCCTC[A/G]CCTTCACCTCTGTCA | 5607 |
rs537306799 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651774 | TTCGATGGACACTCA[C/G]ATTGATTTCATATCT | 5607 |
rs537309805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720317 | ATACACACACATATG[C/T]TTATACATACATAAG | 5607 |
rs537326008 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776369 | TAGGGACAAATTTTC[A/C]GACAGTAGAGACCCT | 5607 |
rs537330883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773327 | TGCTCCCTAACAATT[A/C]CCAAATGGTCATTTG | 5607 |
rs537331767 | snp | A/C | | | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724205 | TCCTAATTTATAATA[A/C]CTTGACAATAAAAAC | 5607 |
rs537332470 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541685 | AAATACAAAAATGAG[C/T]GGGCACGGATGGCGC | 5607 |
rs537332682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628869 | ATGGCAGCCGTGGTG[A/G]TGGTGGATATGGCGG | 5607 |
rs537337565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712276 | AGACTTAAAGATCCA[G/T]ACGTTTGGAGTTCCC | 5607 |
rs537350452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676071 | GGCTCACCAGTCTCT[A/G]TAGTATCCATTAGGG | 5607 |
rs537359445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684365 | TTTAGCAGTGGGGCT[A/G]AACTAGCCCTGTAGT | 5607 |
rs537364065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665560 | TCAACTGTGATGTCA[A/T]ATCTGTCACTAAGGG | 5607 |
rs537364512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570630 | TCTTAATGTAAAGTA[C/T]GAGAAATAATTGAAA | 5607 |
rs537372307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719241 | GTCTAAGCAGTGATA[C/T]GTAAGAGGGCCTTGT | 5607 |
rs537377643 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580037 | AGTTAGGTGGACATA[A/C/T]GCTTACAAATTAGCG | 5607 |
rs537394973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739109 | ACACAGGGAGACCCC[A/G]TCTCTACAAAAAATT | 5607 |
rs537398405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735059 | CATAAAATGCAGAGA[C/T]GAAATTTAAGTGACA | 5607 |
rs537404876 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659718 | TGTATAATAAAGGGC[-/A]AAAAAAAGGCAAGGA | 5607 |
rs537407641 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573654 | GGAAGTCAGGCATTC[G/T]TAGTTACAGGATGTT | 5607 |
rs537412959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591882 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACCTGA | 5607 |
rs537416215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782739 | CTCTGGAATACTCTC[A/G]CTCTAACTCTGGGGA | 5607 |
rs537419357 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732178 | GAAGGTCTAGACAAG[G/T]ACTGGAGCTGCCTAT | 5607 |
rs537430428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574196 | AAGCCACTTAGGGGG[C/T]TGTTCCTTGTGAAAG | 5607 |
rs537452429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782346 | TAAGGCAAATCTGCC[A/G]ATGTAAACAAAATTT | 5607 |
rs537477426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685220 | CAGAAAACAGAGCAC[A/G]TTAAGTAGAGAAACA | 5607 |
rs537478209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591410 | GATGGAGTCTCGCTC[C/T]GTAGCCCAGGCTGGT | 5607 |
rs537481757 | in-del | -/G | 0.007968 | 0.062614 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732960 | TAGCTCTGTGGGGAG[-/G]GGGGGGCTTAACAGC | 5607 |
rs537497110 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725560 | ATGGTCCCTGATGAC[A/T]TGCTGAGCATATACC | 5607 |
rs537520751 | in-del | -/AGAG | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572419 | CCAATCCAGACCCTA[-/AGAG]AGAGTTCTTGGATCT | 5607 |
rs537529052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779323 | TGCATATAATTACAT[C/T]GGCAGAATCACTGTC | 5607 |
rs537529316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775638 | AATAACTAGAATGAA[A/G]TAACTAGTATAAAAG | 5607 |
rs537587183 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623802 | GGGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTCG | 5607 |
rs537618562 | in-del | -/A | 0.442655 | 0.159323 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597186 | AAAGAAAAAAAAAAG[-/A]AAAAAAAAAAACTAC | 5607 |
rs537620013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567660 | TGAGCCACCGCGCCC[A/G]GCCTAAAGTATTTTT | 5607 |
rs537634694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664887 | TGTAAAAAGATATTT[C/T]ATAGTATTTGAAAAT | 5607 |
rs537651511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620912 | AGAGAAGTCGATAGG[C/T]GTAAAGTAAATGAAT | 5607 |
rs537658001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726154 | TTTTGTGTACAAGAT[A/G]TGAGTACAAGGTAAT | 5607 |
rs537666847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715619 | CTCATATCATGTATA[C/T]ACACAAATACACAGA | 5607 |
rs537685635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768607 | ATCATACTTTGCAGG[A/G]CACTTTGTGTAGGGA | 5607 |
rs537687021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560763 | TCTTCTGAAATAATC[C/T]CTCAAGAGATTTCTT | 5607 |
rs537687418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552180 | TTTAAAAGCTATAAT[G/T]AGTAGAACTCAATGT | 5607 |
rs537691450 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771729 | TTCATAACTCCGATT[C/G/T]TTGTTTACCAAATGA | 5607 |
rs537693097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555539 | GACAAAGAATACCCA[A/T]ATTTAAATTTCAATA | 5607 |
rs537723675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614149 | CCAGATCTACTTCCC[A/G]CTCCAGTACTTACAG | 5607 |
rs537735431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606227 | GCCAGCAATCACTGA[A/G]AGATTATCTTTTATA | 5607 |
rs537740446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603499 | ATCCTGATAATTTTC[A/T]TTCTTATATAGTAGA | 5607 |
rs537747276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804759 | GAGCACAGCTTCTCC[C/G]TTTGTTCTTTAGAAG | 5607 |
rs537761560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567298 | GTTAGAATATTCCAC[C/T]TCTGGGATCACGGCT | 5607 |
rs537780222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711499 | ACAAAGTTCACAAGG[C/G]AAAAAAGCCATTATC | 5607 |
rs537787126 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613571 | CCTGGAAACCATCAG[C/T]TTTGAATTTATATTT | 5607 |
rs537815598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589355 | AAAGCATGGGTTGTT[C/T]TTTCTTTTGCCTTAG | 5607 |
rs537819515 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686124 | AGATGGGGCAAATAG[A/G]TGGTAGAGTTGAACC | 5607 |
rs537833469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736520 | GTAACTCTGAAAATA[C/T]ATGACCATGTCTCAC | 5607 |
rs537837582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582682 | CAAAAATTAGCCGGG[C/T]GTGGTGCACACTCCT | 5607 |
rs537849912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789319 | ACTGTGTCTCTATGT[A/G]TACATCTTTGTATAC | 5607 |
rs537864793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615075 | TGATCTTGGCTCACT[A/G]TAACCTCTGCCTGCC | 5607 |
rs537866595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623025 | GAGTATGGCGTGAAC[A/C]CGGGATTTGGAGCTT | 5607 |
rs537876213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588741 | TCCTTTTCTCTTCTT[C/T]GGATATCTCAGTGTC | 5607 |
rs537904283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572530 | ATAGCTACTCACTCC[A/G]TAGAGTAGGACGTTC | 5607 |
rs537906992 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662820 | TCATTTTATTTCCTT[G/T]ACCTGCCCTTTTAAT | 5607 |
rs537910446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651234 | AAATAAATCAATCAA[A/G]ATTTTTATGGATCCA | 5607 |
rs537923752 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624194 | AATACAAAATATTAG[C/G]CAGGCGTGCTGGCGG | 5607 |
rs537929264 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628747 | TGCTTCAGCCAGCCA[A/C]AGAGGTCGAAGTGGC | 5607 |
rs537938624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608857 | CCACTGGGTTGTGTT[C/T]CCTGGAGGAGAGTCA | 5607 |
rs537952448 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702084 | CAAAGTACCTAGCCC[A/G]GTGTCTGACACTAGT | 5607 |
rs537968342 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697681 | AGCATTTAACTTTTC[A/G]TATTAAGAATCTTGC | 5607 |
rs537973286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659136 | TTTTCCCATATTCTT[G/T]TATTTTCTATATGCA | 5607 |
rs537983970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713969 | CTTAGCCAGTTCAGT[G/T]TGTCACTCCAAGTGT | 5607 |
rs537988829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629980 | CGGTGGCTCACTCCT[A/G]TAATCCTAGCACTTT | 5607 |
rs537992293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610170 | CCAAGTTATTTTTGG[A/G]TGTAAGATATAAAAT | 5607 |
rs537993948 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618246 | ACTTCGCTTGGCAGT[C/G/T]GGGGAGATATAACAT | 5607 |
rs537996074 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682301 | AGCTCACTGCAACCT[C/T]CGCCTCCTGGGTTCA | 5607 |
rs537996485 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615699 | AAATTTATTTAATTT[A/C]AAATTTAAAAATTAT | 5607 |
rs537999290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769555 | GAATATAAAGAAAGA[A/G]AAGGAACTGTTGTGA | 5607 |
rs538004744 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741751 | GAAGAAAACAGGGAT[-/G]TTCATTCAAGAAAGA | 5607 |
rs538018251 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542967 | GGTGGACACCTGCCG[A/C]TGTATCTCCCCCAAA | 5607 |
rs538045644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643134 | TGCCCTAGGTATTAC[A/G]ATATGAGGCCAGGGT | 5607 |
rs538047754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751745 | GAACATGGTACTGAA[C/T]GTAAACTTTGATGTA | 5607 |
rs538055234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617754 | TGGAGTGCAGTGATA[C/T]GATCATGGCTTACTG | 5607 |
rs538076391 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759822 | TAACTCCAACCACTC[C/T]CACAAACAGGTTTTT | 5607 |
rs538094557 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550478 | TACCATGAGCATTAC[A/G]TGGAATAATTCTGTT | 5607 |
rs538127140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610619 | CACAGTTTTTTTTTC[G/T]TTGCTCTGTCATTGG | 5607 |
rs538131530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735953 | GATGTGCTAGGTACT[C/G]AAGTCCAAAGGAGGT | 5607 |
rs538138621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709035 | GGGAAAAAAAGATTA[C/T]TCACCTTGACTGATG | 5607 |
rs538147605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788714 | AGACATGGTGGATCA[C/T]GCTTAATTCTAGCTC | 5607 |
rs538151691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692732 | TTCCTTCATCAGAAT[A/G]TGATTGTTCATTGTT | 5607 |
rs538152941 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724553 | ACACGTGCCACCACA[C/T]GCCTCTCATTTTTGT | 5607 |
rs538155985 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546371 | ACCCAGCTAATTTTT[C/G]GCAGAACCTGACACA | 5607 |
rs538157489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550358 | CTGATTGTGATAATA[C/T]TGCAGGACAAAATGA | 5607 |
rs538159006 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761560 | AACTAACAGTCGAGT[C/G]AACATTCAGGAGGAC | 5607 |
rs538173887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716243 | CTACTCGGGAGGCTG[A/G]GGCAGGAGGATCCCT | 5607 |
rs538220312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684582 | AAGAATTTTTCTTCT[A/G]ATTATGGATGAAAGA | 5607 |
rs538223763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565943 | ATCTGTCTTGGTTCT[C/T]ATGATTGAAATTTAA | 5607 |
rs538225778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587894 | TTCTACCTTCTGAGT[A/G]GCTCTGCGTCTTTCT | 5607 |
rs538238749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643634 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCGT | 5607 |
rs538251203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787549 | ATGACCAAATGCTCA[C/T]TATAATTGCTTTAGA | 5607 |
rs538251230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796312 | AAACACCTGAGACTG[A/G]GTAACCTGAAAAGTG | 5607 |
rs538275390 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745031 | AACAGCTAATGAAAG[-/A]AAAAAAAAAATCTAT | 5607 |
rs538282462 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775331 | GTCTTTATATCCTAA[C/G]TGGAAGTATTTTAAA | 5607 |
rs538290794 | snp | C/T | 0.000247703 | 0.0111261 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580864 | CAATGATTATTTCAG[C/T]AAACTGTTTCATCAA | 5607 |
rs538292657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692082 | TAGATAGGAGGACTA[G/T]CTTGATAATTACACA | 5607 |
rs538295065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660056 | CTACTCTGAAGGATT[G/T]TTTATATTTGCCTTT | 5607 |
rs538333172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782252 | GGATTAGAAGTAGCT[G/T]TAGATGTGAAATGAG | 5607 |
rs538340577 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740354 | AAATCAATTGTTTTG[G/T]CCCCTTTCTTTTCTT | 5607 |
rs538346960 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542678 | GCGCCGCGCGTTTTG[A/G]TTCCGGAGTAACAGT | 5607 |
rs538350460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572984 | TACAGGCGTGAGCCA[C/T]CGTGCCTGGCCTGAT | 5607 |
rs538387399 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650383 | CTGATGAGAGCAGAC[A/T]TCCTTCTCTTGTTCC | 5607 |
rs538391240 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552581 | CTGGGACTACAGGCA[C/T]CCACCTCCACACCTA | 5607 |
rs538395214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602558 | ATTTCTAGAAGGGAA[A/G]AAGCATAAGACCATG | 5607 |
rs538403609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594886 | TAATTCCTCAGTGCT[A/G]TAGGATAACTAAACA | 5607 |
rs538412298 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613222 | CATCTTCCAGAAGAG[C/T]AAGGCAAGAACAGTG | 5607 |
rs538412388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678946 | TCCAGCCTGGCAACC[A/G]AGTGACACTGCATCT | 5607 |
rs538423569 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797771 | CACTGCAACCTCTGC[C/T]TCCTGGGTTCAAGCA | 5607 |
rs538426645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566594 | TTAGTCCTTTAATCA[C/T]TCTTTTTCATTGATT | 5607 |
rs538429533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651646 | TGTCCAGATTATTTC[A/G]TTTAAAATAATATCC | 5607 |
rs538460907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698858 | GAGGCTAACATTAAC[C/T]GAGCATTCCCATGTG | 5607 |
rs538464643 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568782 | GAGGCTGAGGCGGGC[A/G]GATCATGAGGTCAAG | 5607 |
rs538503095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559397 | GGCCATTGTGACCGC[C/T]CCTTACCTGAGGCTG | 5607 |
rs538532738 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727205 | ACTCTGGCTCAAAAA[-/AC]AGTTTATATCTTTTT | 5607 |
rs538538311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609523 | ACCTATTCTATAGGT[C/G]TGTAGATTCTGTAGA | 5607 |
rs538544754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559059 | TCTGGTCCTGCCCAC[A/G]TCATTAACTCCGTGC | 5607 |
rs538565379 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551307 | TTGAATGCCCATCAA[A/G]CAAAGTGTTCATTGT | 5607 |
rs538576088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714741 | CCAAAATTTGAAGTA[C/T]TCCCAAATTCGAAAT | 5607 |
rs538600936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616694 | TGTCTTCTACCTGTT[C/T]TCTGAGAGACATAGG | 5607 |
rs538614544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735280 | CCCAATGTGTGGGTA[G/T]CTTAGAAATGTGAAA | 5607 |
rs538665879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699385 | GCCTAAATGGCTAAC[C/T]TCAGTGTAAGAGTAA | 5607 |
rs538669164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594730 | TCCCTTGGGAATGTG[A/T]TAACCTCATATTAAA | 5607 |
rs538687548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728855 | AATAATAGGATGGGG[C/T]TCATTCTCTCTACCA | 5607 |
rs538703447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565238 | CACTGTTATTTATTT[A/T]TTTTTCTCCGAGATG | 5607 |
rs538716541 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772511 | TTGTTTCTTACTCAT[A/C]ATGTCCCCCAGAAAT | 5607 |
rs538720259 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646885 | GTTCTTAATTGCAAG[A/G]TAAGAAATTGTTTTT | 5607 |
rs538733180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588489 | ATTGTATTATAATCA[C/T]CCCTGTCCTCCAGTA | 5607 |
rs538744029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614962 | TCATAACATATTTGA[C/T]TTGAGACCTAAACAG | 5607 |
rs538744053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691349 | TATAAGAAAATGCCA[A/C]GCACATTGCCTGTCA | 5607 |
rs538772557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766257 | CGATTGAGGCTTTTG[A/G]TTAAGGTTGTGTCCA | 5607 |
rs538787382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775559 | GTCTTGTTCTAGACT[C/G]AGCAGAAGATATAAA | 5607 |
rs538789540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767926 | CCTTCTCTACTGATG[A/G]GAATTTTAATTTTAG | 5607 |
rs538797337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622301 | CCAGCCCTCAGGAGT[A/G]GGTGCAAAGGCCCCG | 5607 |
rs538820537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549878 | AAACTCTGGGTTTAC[A/G]TTGCTGGGCTAAGTG | 5607 |
rs538828666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650331 | CTTTTCTTGCTTAAT[A/T]ACCCTGGCTAGAACC | 5607 |
rs538846154 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759199 | GGGTATGAAAATAGC[C/T]GGTGCTGGGGGGTGG | 5607 |
rs538854249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729546 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 5607 |
rs538881088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607935 | CTGGTAAAAATCAAT[A/T]CGTTATGGTAATATT | 5607 |
rs538882212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550274 | TTTTCTTATTTAATC[A/T]TATCTTGGGTGAGCA | 5607 |
rs538888044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657758 | TGTCTATATGCATAT[A/G]TATGTATACTTGCAT | 5607 |
rs538896210 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711422 | CCTTCGGTAAATTAC[C/T]TAACTTCTCTGAGCC | 5607 |
rs538913623 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715595 | TTAAAGTTTTTCCAA[C/G]AGCACATACTCATAT | 5607 |
rs538921717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617640 | CAGGTTGTTTCTCCC[C/T]TCTGTCTTGTGTGGA | 5607 |
rs538928109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669370 | AAGGGTAGGTTGCGT[A/G]TTAATCAAAGAAACC | 5607 |
rs538937802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795588 | AGAGAGCATGCTATG[C/T]ATAACATCAGATCTT | 5607 |
rs538960151 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709907 | TTCTTATTTTCACTG[A/C]GTATGCTGTACAAAT | 5607 |
rs538960527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748030 | TACTAAAAAGTGTTG[C/T]GTGAAATTAACATTC | 5607 |
rs538965485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750848 | AGTGGGATTTACCCC[A/G]TTGTGAAGTGGGTAT | 5607 |
rs538994204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802653 | ACAGACATGGCTGTG[C/T]AGAAATGGTGCTAAC | 5607 |
rs539016855 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572470 | AGAGTGAGTCCACAG[A/T]GCAAAGTGAAAGTAA | 5607 |
rs539063871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683685 | GAGAAGCTTGAACCT[C/G]GGCATTGGAGGTGGC | 5607 |
rs539066891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587333 | ATCATGCGGGGCCTC[A/G]TAGGCCCTGTAATGT | 5607 |
rs539091384 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579269 | CAAATACTTGTGTGC[C/T]GAGGACAAGTCATTT | 5607 |
rs539113930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720777 | GTGGCTCGAAAGCAC[A/G]TATGCTCCAGTCACA | 5607 |
rs539147487 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773863 | TCACATTTGAGAAAA[C/G]TTGGAACAGGTTCTA | 5607 |
rs539152812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717824 | TCCTTTGTGGTGCCT[A/G]GTGTTCTAAGCTGTG | 5607 |
rs539160630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762559 | ATAAGTCTTTTAAAT[G/T]ACAGACAAAAAAAAA | 5607 |
rs539172000 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713717 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACTCCGT | 5607 |
rs539173407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770901 | AAATTTTATTAACAC[C/T]GTTTCTATTTATTTA | 5607 |
rs539177631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576573 | TCTGAGTCTAGTACT[A/G]GAGATTCCATTAGCA | 5607 |
rs539182039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608671 | TCTGAGAAAGAGAAG[A/G]TTAAAGGGCTCCATG | 5607 |
rs539192703 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601011 | GTACCTTTAACTGGC[C/G]TGAAGTTTAATGCAT | 5607 |
rs539208691 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740374 | TTTCTTTTCTTCCAT[G/T]TCCCATCCTCCCACT | 5607 |
rs539212068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546183 | CTGTTCTCCAGGTTT[A/G]CTTCATCTCTTCATC | 5607 |
rs539235819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713808 | GGAGAAATTTGATGG[C/T]GAGTTTGTCATTTTG | 5607 |
rs539273827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763216 | ACACACCGAGAAGTA[G/T]GTCAGTTCTATCTGC | 5607 |
rs539276049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612571 | GGATGGTATAAGATA[C/T]GATGGTAGTTTGTGT | 5607 |
rs539283089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546842 | GGCCGAGGTGGGTAG[A/G]TCGCTTAAACTCAGG | 5607 |
rs539284013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751638 | CATTTTTAGAAAGAA[A/G]TGTTTCTAACATCTA | 5607 |
rs539284951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754464 | TATTGAGCTCCTCCT[C/T]GGGCTGTGATCTCTG | 5607 |
rs539302619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742641 | AATGTCTAAAATCTT[C/T]AAAACTTAGGTACTT | 5607 |
rs539312346 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803252 | GGGGTCACCTCCCAG[C/G]TGGACTTGGTATTAT | 5607 |
rs539324841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565799 | ATTTTTTGTAGAGAT[A/G]GGGTCTTGCTTTGTT | 5607 |
rs539333435 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590286 | GATCAAACTTGAAGT[C/T]TGAGATTCTCTCAAA | 5607 |
rs539334781 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790727 | CACATAAAAACAAAC[-/A]AACAAAAAAAAAAAA | 5607 |
rs539336664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601795 | CCTTGGTATAGAATT[A/T]GATTTCTCAGGCTTA | 5607 |
rs539341944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791726 | TTGTGACACTGAAAT[A/G]AGATAATGAGCTTGA | 5607 |
rs539345492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800196 | CATAAATTATTTAAC[A/G]TCTCTAATCTGAAGT | 5607 |
rs539345584 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783436 | CTTGTGCTGTTTTCT[C/T]ACCGCCAGATGGTGA | 5607 |
rs539369625 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770377 | ATTCCCCTCTTCCCT[A/C/T]GTCCTGCAGGACTCA | 5607 |
rs539380803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647549 | CCCAGGAGTTTGAGA[A/C]CAGCATAAGCAATAT | 5607 |
rs539398683 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622079 | ATCCCTGCTACCCAG[A/G]GGTGGCAGTGAGCCG | 5607 |
rs539403172 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770226 | GGAGCCACAGGGGCC[C/G]TCAGAGCCTCTAGGC | 5607 |
rs539406047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603357 | GTTTTTTAATTTGCT[A/G]GAATGCTGTGTGTAA | 5607 |
rs539413433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700740 | GTTTAGGATAGACAC[A/G]TGGAGCTTGCTGTTG | 5607 |
rs539418897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568740 | GGCTGGGCGCGGTGG[C/T]TCACTCCTGTAATCC | 5607 |
rs539436560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724096 | GGCAAAATTAAAAAG[G/T]ACATTAAAGCTTCAT | 5607 |
rs539437711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752476 | CAAGGTCAGGGGTTC[A/G]AGGCCAGCCTAACCA | 5607 |
rs539459429 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652771 | AAACTGAAACTCTAT[A/G]CCTATTAAATAAGAA | 5607 |
rs539459702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777671 | CTGTTCAGTGGCAGC[A/G]AGAATTTCAGAGAAA | 5607 |
rs539466255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804242 | GTGAACAGCTGCCAG[A/C]AGCTACCAAGTCCAC | 5607 |
rs539471968 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688990 | AAGATACTGTGCTCG[G/T]AAGGGATACATTTAA | 5607 |
rs539477633 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692317 | CTTACATTTTACCTT[C/T]GGTTAAAAAAAAATG | 5607 |
rs539478039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654224 | GTTGTTAGGTCCATG[A/C]ATGTTTATAATTGTT | 5607 |
rs539484423 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546790 | GACTTCTGGGCCAGG[A/G]GTGGTGGCTTAGGCC | 5607 |
rs539484729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553037 | TTGGCTTCCAGTTAG[C/G]GTTCATAATAATAAT | 5607 |
rs539487845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671045 | GACTGACTGCCTCAC[A/T]GGGTGACCCCAGAAA | 5607 |
rs539492007 | snp | A/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723312 | TATTTGTTATTTAAA[A/T]TATAAAATCCAACAT | 5607 |
rs539495287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575637 | AAGCAATAAATATAC[A/G]TTTTATGCCCTGAGT | 5607 |
rs539544750 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760306 | AAGAAAGAAGTGAAT[A/G]CAAAATGTTACAGAA | 5607 |
rs539550702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717029 | GGCAGCAGCAGTCAA[A/G]TATTCTGACTCATGG | 5607 |
rs539551165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744370 | ACCATATGATTTAAT[G/T]TTATATTTCTTCTTT | 5607 |
rs539552985 | snp | A/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721167 | AAGTTCCAGGGTACA[A/T]GTGCAGGATGTGCAG | 5607 |
rs539605440 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602104 | GTCTAATGATTTTTG[C/T]GGCTACTATTCTCTT | 5607 |
rs539615479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589997 | TAAATAGCAGCTGCT[A/G]TTATTATGTTAACTG | 5607 |
rs539644595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604825 | GCTTGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 5607 |
rs539683859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738975 | GTGTGAAGTAAAACT[A/C]TGAATCAAATATCAA | 5607 |
rs539695670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730926 | CTTTGTAACTCTGAG[A/G]TGTCAGTTTCCTCAT | 5607 |
rs539700678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723244 | TTTTTATCGTGTTAT[A/G]TATTTGGCAATTGTT | 5607 |
rs539715161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631815 | TCTGTCTTGAATTGC[A/G]CTTCTGACTGAACCC | 5607 |
rs539716185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624888 | CACCTGGCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 5607 |
rs539720656 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769576 | ACTGTTGTGACTTTT[A/G]GTGACATGTTTTTCC | 5607 |
rs539722735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553838 | GAATGGCGTGAACCC[A/G]GGAAGCGGAGCTTGC | 5607 |
rs539723139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776532 | TAATGCAAAGATGGT[A/G]GAGAAATTTCCCTTA | 5607 |
rs539730551 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626075 | ATTTGTCTTTATATT[C/T]CAGTTCTTGATTAGT | 5607 |
rs539731083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746729 | AAGCCAGTCAACCTG[A/G]GACAGAGGTTTCTGA | 5607 |
rs539732177 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751978 | TTGCCTCTGTTCTCT[A/G]TGGGCACTCCTCATT | 5607 |
rs539781065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738035 | TTTTGTATTTTTAAT[A/G]GAGATGAGATTTCGC | 5607 |
rs539806183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760453 | TGCTGAAAAAAATCT[A/G]TATTTTTATTATTTC | 5607 |
rs539808259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669713 | CTTTTAAGAGAAAGG[C/T]GTCAAGGTTGCTTAA | 5607 |
rs539829981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567370 | GTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGAGT | 5607 |
rs539840392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761534 | AGGTGGCAAATGGCA[G/T]TAATTATTTTAACTA | 5607 |
rs539841127 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609951 | TGGACAGGGCTTGAT[A/C]ATGCTGGGTCTTTTA | 5607 |
rs539847195 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763332 | TAACAAGCATTGATT[G/T]AATTTGTACAAATCT | 5607 |
rs539863238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722483 | AACACCGGTAAATTG[C/T]TGTTATATCCTTTGG | 5607 |
rs539863782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660668 | GTTGCATGCTTTCTA[C/T]ACAAATATTATGTCA | 5607 |
rs539879022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760904 | TACCCAGCAGCTTGG[G/T]CTGGGGGCACTGCTC | 5607 |
rs539886118 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722446 | GTGTTCTTTGTTGTC[A/G]GTTTAACCTCCAAAG | 5607 |
rs539890466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551544 | TGCTATGTTGTCCAG[G/T]CTAGTCTTGAACTCC | 5607 |
rs539897558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645530 | CTCTCTGCTTATTGC[C/T]TAGTGTCTGATCACA | 5607 |
rs539916239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798225 | ATTCTCCTCTGGCAT[A/C]CTCCCTCCTGATCCC | 5607 |
rs539923877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753138 | GGACCACTGGATATC[C/T]ATATGTATGTGAATA | 5607 |
rs539939612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700158 | ATCGTTGTAAACAGA[C/T]GGTTCTGGAGTTAGT | 5607 |
rs539944405 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652227 | GTGTGTCATTAGTGC[A/G]TGTTTTTTTTAAATT | 5607 |
rs539967947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752245 | CAATTTTTTGTATTA[C/T]TAGTAGAGACAGGGT | 5607 |
rs539982154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804045 | AGCCCCAGCCTGTGA[C/G]GTGCCTCACAGGATC | 5607 |
rs539982859 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571063 | TGACCAATGAGAGTC[A/G]TTACTATGTCTATAT | 5607 |
rs539995205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686860 | GGGGGTAGGAGGGAG[A/G]TGGTGAAAACAGAAT | 5607 |
rs539997691 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550250 | ATGATGATACTGAAC[C/T]GAGTAATATTTTCTT | 5607 |
rs540001977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783421 | ACAGTCATGTCTTTG[C/T]TTGTGCTGTTTTCTC | 5607 |
rs540005921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790856 | GGCCACTGATAGTTA[C/T]GACTATGGAACTGCC | 5607 |
rs540008853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544638 | TTGTGCCCATTCTAC[A/G]TGCAGAATAACTGAG | 5607 |
rs540015629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583630 | CTGGGTATATTTCCT[A/G]TGTCTACCTAGTTGG | 5607 |
rs540042797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790407 | CATTGCATTATATCA[C/T]GCAATAAAAATACCC | 5607 |
rs540060024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694196 | AAGGGAAGTTATTTG[G/T]TTTCATAAAAATACT | 5607 |
rs540068832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545184 | TCTCTGTGTCATTCT[C/T]GGTTATGTGCCCCAC | 5607 |
rs540074455 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628177 | AAAAGATATTTGTTG[A/G]TGGCATTAAAGAAGA | 5607 |
rs540102900 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704092 | GAACTCTATGCTATG[-/T]TTTTTTTAATAAAAT | 5607 |
rs540114396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784249 | AGCCAGGAAAAACAC[A/G]GGACTGTCCTACTGC | 5607 |
rs540124906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729821 | TGAAGCACATGAAAG[C/T]TGTGGTCAAATTTGA | 5607 |
rs540131203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694489 | TAAAGATTTAGGGAT[A/G]GAAAAAACACATGAA | 5607 |
rs540133431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790498 | GTCTGTAGGCTGTGC[A/G]CAAGTGCAACAGTTG | 5607 |
rs540148504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680091 | ATGAAATCTTTGTGC[C/G]TGACTTCTTTCACTT | 5607 |
rs540153595 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783090 | ACATGGAGAGAAGCC[A/G/T]ATGTGGGAATCACAG | 5607 |
rs540157355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631083 | GGTGACATTCAGACA[C/T]CTGAAGATCTTTTAA | 5607 |
rs540167624 | in-del | -/TTAAAAATTATATTTTTCATTAGCTGA | 0.0248432 | 0.108648 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615704 | TATTTAATTTAAAAT[-/TTAAAAATTATATTTTTCATTAGCTGA]ACCACAGCTGGTTTA | 5607 |
rs540169763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798367 | TTAAACAGGCCAGTG[A/G]CACAATTCTGCCATT | 5607 |
rs540171501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645697 | TAGATTGGGACCACC[C/T]GATCATACTACACAC | 5607 |
rs540174059 | snp | A/G | 3.32105e-05 | 0.00407482 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693594 | TTATGCAAAAATAAT[A/G]TTTAAAACCAACATC | 5607 |
rs540176353 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630335 | TTTTTCATAAATGGA[C/T]ACATTTATATTTATT | 5607 |
rs540187465 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551331 | TCATTGTGAGATCAT[-/G]ATGATAATTATTGTT | 5607 |
rs540191575 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764376 | AGAAGGTATCTCACA[C/T]GCTGCAGACTCTTTT | 5607 |
rs540192383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789862 | TTGTCTCTTCCTTCA[C/T]CTTGTTGAAGATTGA | 5607 |
rs540224973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751106 | TGGAATGGCCAAAGA[C/T]GAATGTTAGAGCCAC | 5607 |
rs540226898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742138 | CCTCGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 5607 |
rs540232429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617022 | GTGTCCTTCATAGAA[C/T]AGTGGCAATACTATC | 5607 |
rs540235488 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611403 | TATTTGCAGAGCACA[A/G]CAGCTGGGGTAACTG | 5607 |
rs540252360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668722 | TCCCTGAGGATAAAA[A/G]ATAGAAATGCAAGGG | 5607 |
rs540260111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750511 | TTGCTGTGATGCAGT[A/G]TTCCTCATAGGGTGG | 5607 |
rs540269373 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698264 | GCGATTGCAGCTCAC[C/T]GCAACCTCTGTCCCC | 5607 |
rs540277443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804472 | GAGGGCAGGAGAGGC[C/T]GGCATCTCCACCGGA | 5607 |
rs540289166 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574309 | GGGCATAGTGGTTCA[C/T]GCCTGTAATCCCAGC | 5607 |
rs540290147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636428 | AAAAAAAAAAGTATG[A/C]AATATAGTTATAATA | 5607 |
rs540313625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602998 | AGAAGTGGAAAAAAC[A/G]TGCCCATCCCCCAAG | 5607 |
rs540315442 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610248 | TTTTAGAGGCTTTTT[A/T]GTAGATGTTAAAACG | 5607 |
rs540317509 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575373 | TGGAGGTGGCGGGGC[A/C/G]GGGGAGGGCAGTGGG | 5607 |
rs540344737 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761022 | TTCTCAAAAGAGATT[A/C]CAAACTGGTCGGCTG | 5607 |
rs540351693 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736715 | CTTACAATTTTTAAA[-/T]AATCAATTTAGCCCC | 5607 |
rs540404380 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633145 | CCTTGGTTCTCACTG[A/G]GTGTGGCTCTGTTGT | 5607 |
rs540412686 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594147 | ATATCCTATATACAG[C/T]TAAGGAGAATCTAGT | 5607 |
rs540420806 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744576 | TCTCTAAGTTACATA[C/G]GTAGATTCATTTTAG | 5607 |
rs540422846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677540 | TGCTGTCTTACATCT[G/T]ATTTATGCATATAAT | 5607 |
rs540427211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629069 | ATACTTTGCCAAACC[A/C]TGAAACCAAGGTGGC | 5607 |
rs540431813 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628863 | GCTTTGATGGCAGCC[A/G]TGGTGATGGTGGATA | 5607 |
rs540436513 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600995 | TCCACCATTAGTAAG[C/T]GTACCTTTAACTGGC | 5607 |
rs540454029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603584 | GGCGGTGAAGATACC[A/G]AATTGCATAACCGCT | 5607 |
rs540493031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630475 | GGGAAAAAAAAAGCA[A/G]AATGGCTCTGTACAC | 5607 |
rs540501012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737517 | GATGCTAAGAACCCA[A/G]CCCTCTTCAGTGCCA | 5607 |
rs540511808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775268 | CATTTAGTTGTTTAG[A/G]TATTTTATCCCCTCT | 5607 |
rs540514269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589616 | AATGCAATGAATCAA[A/T]ATGTTATTAATTCAA | 5607 |
rs540537820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745339 | GAAGGCAGACCCAGA[A/G]TAAAGATAGGCATTC | 5607 |
rs540562689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629469 | AATAAATGTCTTTTT[A/T]AAAAAAATATTTGTC | 5607 |
rs540593097 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796172 | ATTTATTGTTTGTTG[A/G]TATACTTGAGTTTTT | 5607 |
rs540602519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550452 | AAAACATAGCAACAA[A/G]GTAGAGCTTTTACCA | 5607 |
rs540623937 | snp | C/T | | | missense, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703401 | GCTTAGGAATCTCTT[C/T]TATGGAGGTACGTTG | 5607 |
rs540646250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706594 | GAGGTTGTAAAGAGG[A/T]ATCAGATTATGATCA | 5607 |
rs540657773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750631 | TCGTGCCTAGAATCT[A/G]CTAGTTTCTCGGGTA | 5607 |
rs540658997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746998 | CATACCAAGTATAAA[C/T]GTATACAAATACAGT | 5607 |
rs540684487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633374 | ACACTGTTATAAATC[A/G]TCTAGAAATCTATGA | 5607 |
rs540688429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732293 | GAAATGAAAAGGATT[G/T]CCTGCTAAAAATTGT | 5607 |
rs540688707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740242 | GCATAAGGACTTAAT[A/G]AACATATATGAAATC | 5607 |
rs540701229 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563706 | AAATCTACTTTCAAC[G/T]GGAGATCTCTCTCAC | 5607 |
rs540715585 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594962 | CATCAATAAATTTCT[A/G]GGCTGAACACTGACA | 5607 |
rs540719806 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710181 | CCCATCTTTAGCATA[C/T]GCATAGCATACGCAT | 5607 |
rs540721778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675096 | CAATTGCATTCCTGG[A/G]CATTTATCCCAGAGA | 5607 |
rs540728040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739124 | GTCTCTACAAAAAAT[G/T]TAAAAACCAGCTAGG | 5607 |
rs540738539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549968 | CTCATATTTCCTGTA[A/G]GATTTGCCACATGTT | 5607 |
rs540745467 | in-del | -/GAGGGAGCGGTGAGCAACCACAATTCATCTTCATGA | 0.030278 | 0.119257 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802244 | AAAGCCCAGGTGGAG[lengthTooLong]GAGGGAGCGGTGAGC | 5607 |
rs540759676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698961 | TTATTTATTATTACT[C/G]TCTTCATTTTACAGA | 5607 |
rs540764231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591649 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCG | 5607 |
rs540767412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691713 | TGAATTCCTGAAAAG[G/T]CTCATTGTTGTCACT | 5607 |
rs540794440 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782404 | GGGGGATTGATTTGA[A/G]GGCACCGAGGAATCG | 5607 |
rs540803457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733236 | TTATACAACCGCCAG[C/T]GGAATTTTTTCGTTT | 5607 |
rs540822534 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724881 | CAGTGGTGACACTCT[A/G]TAAGAGAGGAAGTGA | 5607 |
rs540833623 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763207 | TCCCTTGTAACACAC[C/G/T]GAGAAGTAGGTCAGT | 5607 |
rs540844950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692810 | CAAACTTCATTGATA[C/T]GCAGCTTTGATATGA | 5607 |
rs540848840 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763235 | AGTTCTATCTGCATC[A/G]TGAAATCAAAAATAA | 5607 |
rs540870702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785795 | GGATGGTCTTTCAAA[A/G]CTTGCAAATCAGTCT | 5607 |
rs540881498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721627 | ACAAGCTTTGCCACC[A/G]ACTTACAGTATGACC | 5607 |
rs540894326 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623809 | TCCATGTTGGTCAGG[C/T]TGGTCTCGAACTCCC | 5607 |
rs540900898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585822 | TCATTTCTTTTTAAA[C/T]GATTCATTTTGAGCA | 5607 |
rs540913702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771880 | GTGATAGAAGCAGCA[A/G]TCTCTTTTCATGACT | 5607 |
rs540919514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718837 | TTTTGATACAGGCAT[A/G]CAATGTGTAATAATC | 5607 |
rs540950114 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553898 | GCAGTCCGGCCTGGG[C/T]GACAGAGCGAGACTC | 5607 |
rs540958226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674601 | TCTTTCCCCATATTG[G/T]TCATTCATTCTATTT | 5607 |
rs540963747 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729003 | AAGTGGAAGAGAAAT[A/C/T]GTCCAAGTTGTTAGG | 5607 |
rs540978385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591081 | GCTGGGTGTGGTGGC[C/T]CATGCCTGTAATCCC | 5607 |
rs541000823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639563 | CCCCCTGCCGGCGCT[C/G]CTCACTGCTCTCAGA | 5607 |
rs541005293 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725676 | TAGGTGTGAGACTCT[C/T]CTCTTGCTGGTTTTC | 5607 |
rs541006225 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647699 | ACATGGCGAAAACCC[A/G]TCTCTATAGAAAATA | 5607 |
rs541011743 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767625 | GTAGAATCTTACAGG[C/G]TTGGTGATATATATG | 5607 |
rs541038060 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752240 | CTGGCCAATTTTTTG[C/T]ATTATTAGTAGAGAC | 5607 |
rs541043427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799647 | TACGCAGAGGTGAAC[A/G]ACTGCAGGCCTCCTG | 5607 |
rs541049713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746293 | GCTGCATGTTCTCCT[C/T]AGAGAATGTTGTCAT | 5607 |
rs541062266 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647017 | TTGACCTGAATATTA[C/T]GGCAAAATACAGATT | 5607 |
rs541111131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785235 | CAGGTGTGAGCCACC[A/G]TGCCCGGCCCCGAAC | 5607 |
rs541116478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680713 | TCATAACCACCTATT[A/G]TCTACTTGGGCTGTC | 5607 |
rs541117802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724274 | AAAGATACAGAATGG[A/C]CCCAGGTCTGCCTGT | 5607 |
rs541118793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792752 | TCTTTTCCGCCCCCC[A/G]CTTTGACCATAAATC | 5607 |
rs541126898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688961 | ATCATTTAAAAAGCT[A/G]TCAACCAGTGAGCAA | 5607 |
rs541139252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554883 | AATTTGCGTTTTTGG[A/G]TTATTTGTGTTATAG | 5607 |
rs541150665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777951 | ATAGTGGCATTAGAA[A/G]TACAACAAGTTGGCA | 5607 |
rs541159285 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583920 | CTGGGCATTTTTTTT[A/T]AATTTTTTAATAGCG | 5607 |
rs541189902 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804136 | GGGTCTCCAGTGCCG[C/T]CACGACCCCCCGCCT | 5607 |
rs541190847 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742110 | CATGTTAGCCAGGAT[G/T]GTCATGATCTGCCCT | 5607 |
rs541192924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673826 | TATGACATATTTTTG[C/G]TTTCTGGAGGATCAG | 5607 |
rs541204932 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677877 | TGAAGAAGGAAAGGG[C/T]ACGTTTGTTGCCTCC | 5607 |
rs541208481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731193 | AAAGTGGGGAGGAGG[A/G]GCCGGCTTCAAGACT | 5607 |
rs541220787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570049 | ACCAAGGTAATAACT[C/T]TGAAAGTTTCAGCTG | 5607 |
rs541221245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578443 | CCTTTACAGCATGTC[C/T]TTGATGGTGAATTAC | 5607 |
rs541248000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562352 | GCCAACAATTTCATT[C/T]TGGGTTAAAAATGAG | 5607 |
rs541251341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800857 | TAGCCCATGCTTGCC[A/G]TGTAAGAAGTTGAAT | 5607 |
rs541263922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689735 | CAGTTTTGTTGTTTT[A/G]TTATTTTGTCTTTCC | 5607 |
rs541272399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617894 | GATGAGGTATCATCT[A/G]TGTTGCCCAGGCTGG | 5607 |
rs541276400 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709159 | CCTCCTGTGGATTAG[-/T]TATGGAATCATTAAA | 5607 |
rs541276856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619350 | TTGATTATTGTCAGT[C/G]AGCCCCTATTAGAAG | 5607 |
rs541295904 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785784 | GGAGAGGCTAAGGAT[G/T]GTCTTTCAAAGCTTG | 5607 |
rs541309067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605055 | TTGGCCATGGGACTC[C/T]TTTCTTTTTTTTTTT | 5607 |
rs541355771 | in-del | -/AGTTTAAGATGTATTTAGAAAGAAG | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590216 | TTTGACCATAGCAAA[-/AGTTTAAGATGTATTTAGAAAGAAG]AGTTTAAGATGTATT | 5607 |
rs541368961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577845 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCGGG | 5607 |
rs541369996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680190 | ATAGTATTCCATTGT[A/G]TGGATATATCACATT | 5607 |
rs541384774 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714342 | TAAGAATTATGAAAC[A/G]TTATCTAGCCTTGGC | 5607 |
rs541388615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776873 | CAACTCCCCATCCCC[C/T]CTCCACTTCAGTGTC | 5607 |
rs541392132 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568899 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 5607 |
rs541411528 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604991 | ACTACTGGTAATGGT[A/C]GTACTAATAATAGAA | 5607 |
rs541425617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783585 | TAGTGCACTCGTCAC[A/G]CTTTGTGGCAGTAAC | 5607 |
rs541434448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631356 | CCCCATTGCCATGGT[C/T]TTGGATCGGGCTCAC | 5607 |
rs541455493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753928 | TAGCGGCATTATTCA[C/T]AATAGCCCAAACGTA | 5607 |
rs541466562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597935 | CAGGCCGGGCGTGGT[C/T]GCTCATGCTTGTAAT | 5607 |
rs541481164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710090 | TTGCCTTGAATTCCT[A/G]GGTTCAAGCGATCCT | 5607 |
rs541486250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639498 | CCACAACTGATAAGT[A/G]GTGGAGCCAGGATTT | 5607 |
rs541488779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618839 | TGCTAGGATTTTACT[A/G]CAAAAGCCTCCCAAC | 5607 |
rs541503391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546320 | TTCGAATGAAGAGGC[A/C]TGAACCCCACAGGGG | 5607 |
rs541505407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762587 | AAAAAAAAAAACAAG[C/T]AGACTAAATGAAGAA | 5607 |
rs541510146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625849 | CTCCTTTTAATTCAC[G/T]TGGAAATAGGACACC | 5607 |
rs541524339 | in-del | -/TGTT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640992 | TTCTACCTTTTTGTC[-/TGTT]TGTTTGGTGCAGGTA | 5607 |
rs541524714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769985 | ATAGCCCCTACTGAA[C/T]GGACGTACGAAGCTT | 5607 |
rs541544188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746054 | GATATTGCTGTTTTT[C/G]TCTTTCTTTTAATGA | 5607 |
rs541573584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625067 | TGCTGTGAAAGAAGG[A/G]GATTAGGTTAAATAA | 5607 |
rs541583481 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646793 | GTTCTGTTCTTTTAA[C/T]GTTTCAATAGCCAAA | 5607 |
rs541594557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778208 | CTAAATTAAATTGTC[A/T]CTGGTAGCTTTTCTG | 5607 |
rs541594598 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806302 | CTCGGCTGACTGGCC[A/G]TGCGAGTGATGCCGG | 5607 |
rs541652689 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587902 | TCTGAGTAGCTCTGC[A/G]TCTTTCTACTCGCCA | 5607 |
rs541655574 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739098 | CAGCCTGGGCAACAC[A/G]GGGAGACCCCGTCTC | 5607 |
rs541671078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791905 | CACTGATCTGTTCCC[C/T]TCACCACCAGGGAGA | 5607 |
rs541698832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799162 | CGACAGAGCGAGACT[C/T]CGTCTCAAAATAAAA | 5607 |
rs541703472 | in-del | -/CTTGT | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689696 | GGTTCTTATTTACAC[-/CTTGT]CTTTTGGAATATAGT | 5607 |
rs541721760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626678 | TCAAGGTGGGAGGAT[C/T]GCTTGAGGCTTGGAG | 5607 |
rs541730992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561250 | ATGTAACATTACATC[A/G]TTTGTACTTTGTTTT | 5607 |
rs541752057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654546 | CTAACAAGGTGAGAT[A/G]TATCTATCCCATTCT | 5607 |
rs541753399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805461 | GTGATGAGCTCGTGG[C/T]GAGGCCATGCGGCTC | 5607 |
rs541763782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597564 | TAATATTTAAATACA[A/G]TATTCCATAAGCTTC | 5607 |
rs541766768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732206 | TATAGTTAATCATGT[A/G]GATCCAAATTCAGTT | 5607 |
rs541820425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582900 | TAAAAAATTTTTTTT[A/G]GTTATCTTCATCCAA | 5607 |
rs541825421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554170 | ACTCAAGCAATCCTC[A/C]CACCTCAGCCTCCTG | 5607 |
rs541831289 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757678 | ACAGTCATATATGCA[A/G]ATCACTAAACTGCAG | 5607 |
rs541846455 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629697 | TTCCTATCCTAACAC[C/T]TACCAGATGAGAGGA | 5607 |
rs541848859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589035 | TAGTTTGTAGAGACG[A/G]GGTCTCACTGTGCTG | 5607 |
rs541849374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653834 | TTTTCCTCTAAGCAC[A/G]GCTTTAGTTGCATCC | 5607 |
rs541877741 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588996 | AGTGTTTTTTTTTTA[-/T]TTTTTTTAAATTTTT | 5607 |
rs541878273 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549979 | TGTAGGATTTGCCAC[-/AT]GTTAGCAATAAAGAA | 5607 |
rs541883348 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596431 | AAAAAACTCAACAAC[A/T]ACAGGAAAACCTTTT | 5607 |
rs541891578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736163 | AGGTAATGTGTCAGG[A/G]TGGAGATGGCAAGTG | 5607 |
rs541894142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722745 | GTGTCTGAGTGTTCC[A/G]AAGTGGCTGCTGCAT | 5607 |
rs541908811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791213 | GACTTTGAAGCTTTG[G/T]AAGAGGAGACTCTTC | 5607 |
rs541925513 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695111 | CTGGGGACTGTTGTG[A/G]GTTGGGGGGAGGGGG | 5607 |
rs541926782 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791460 | GAGTGCAGTGTCCTT[A/G]TTTATAAAATAGGTT | 5607 |
rs541926925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729785 | AAAAAAAAGAAATGG[A/G]TTACTGCCACATTTG | 5607 |
rs541928070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730284 | AGTGTCACTGAGGCT[A/G]AGTTATGGAATAACA | 5607 |
rs541931681 | in-del | -/AAATGATGGAATCATTTGGAATCATGTGG | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564329 | GTTCTATACAAATGC[lengthTooLong]AAATGATGGAATCAG | 5607 |
rs541935935 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590432 | CCCTCCCTCCCTCTC[C/T]CTCTCCCTCCCTCCC | 5607 |
rs541939244 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621460 | AAAAAGAACAAAAGT[G/T]AATTAAGTGAAAATT | 5607 |
rs541955417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582438 | TTCTTCACAAGGAGT[A/G]GTATTTTACAAACTG | 5607 |
rs541956095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553454 | CAATAAATACAAAAC[A/G]TACCCACAGACAAAA | 5607 |
rs541963807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680835 | GAGACACATGTTGTG[A/G]TTGGATAATGTTAAC | 5607 |
rs541977822 | snp | G/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547281 | TCCTAAAGTCAAGGA[G/T]CAAGTTTTATTGTCC | 5607 |
rs541986803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694748 | ATTTGACCCAGCCAT[C/T]CCATTACCAGGTATA | 5607 |
rs542006300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723286 | TTCACGCACAGGCAC[A/G]CATACAAATATATTT | 5607 |
rs542006758 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576959 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 5607 |
rs542025109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687993 | AAGTATCTGAGCTGG[G/T]GGGTATTGCTACTGC | 5607 |
rs542028338 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725513 | GTGGGCAAGTTTCCT[C/T]TGTCTTTAAGCCATG | 5607 |
rs542041449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738294 | GCATAAGGCATGAGG[C/T]GACCTGGACTCCAGG | 5607 |
rs542044768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715929 | ATGTCCCATCCCTGG[A/G]GACACATAAGTAGGG | 5607 |
rs542054895 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792265 | TCCCCTTAATTGTTA[C/T]GAGAAGAGTATTTAA | 5607 |
rs542065492 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544144 | CGATTTGCTTGCCTC[A/C/G]GCCTTCCCAAAGTGC | 5607 |
rs542072513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619856 | GGATCATTTGAGGCC[A/G]GGAGTTCAAGACCAG | 5607 |
rs542072814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590965 | GCTCCCAGACTCTCC[C/T]CTGTTGGGGGAGGGT | 5607 |
rs542078824 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690127 | AAAAGATTGTACACC[A/C]CTAGTTTAGGACATC | 5607 |
rs542100678 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571611 | CAAGATTTTTTTTTT[A/C]AAGTACTTTTTAAGA | 5607 |
rs542101988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769276 | TTGTTAATTACAAGA[C/T]CATTTGTGTGTTACT | 5607 |
rs542103126 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721585 | ATTGCCAAAACATTT[A/G]TAGAGCCCAGTGTTC | 5607 |
rs542117998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725109 | GAGTTCACCAGTTCA[A/T]GCACTGGCACCTGTT | 5607 |
rs542141205 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758012 | GGGCAAGTATTATGA[G/T]ATATAAACCAAGGGC | 5607 |
rs542146567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585541 | TCTTTTCAAAGTAGT[G/T]TAAGTGATAGCAGAT | 5607 |
rs542155291 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571495 | TCCAGATATCTCAGT[C/T]GCCTTGTTTTATGGT | 5607 |
rs542156484 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724407 | TTTATTTATTTATTT[A/T]TTTTTTGAGTTAGGG | 5607 |
rs542159278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610470 | ATGTGTTCGAAAATC[A/G]TAGTCTCTTGGTTGG | 5607 |
rs542173688 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763464 | CTGCTTTTTTCTCCC[-/CT]GTCTACATTCTGTTA | 5607 |
rs542182292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575838 | TATCCAATGAGTGAG[A/G]GTTAGTTCTCTCCCT | 5607 |
rs542212312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579485 | TTCACATGTTTATGC[C/T]GTATGTATATAAGTT | 5607 |
rs542215761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782973 | AGTGGGTTAAGCACC[A/G]AAGGAAGGTGTAAGG | 5607 |
rs542244451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586734 | GTGGGTTTGTCTAGC[A/T]ACAAGCTAATTAACC | 5607 |
rs542314619 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660495 | TCCTTGGTCATTTCT[C/T]TGAAAGTGTACTGAA | 5607 |
rs542316397 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729978 | TACCAGAGTTGGGGC[A/G]GGAAACAACTGTATT | 5607 |
rs542327678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776038 | GAATGGTCTCCTGTT[C/G]ATGTATAGGGAGGTC | 5607 |
rs542327769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783480 | CGAAACCCAACTGGC[A/G]CAACCTCTGTGAAGC | 5607 |
rs542337088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630412 | TTTGATGAACTGTTA[C/T]GATATAGTTTATCTG | 5607 |
rs542367442 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769807 | CAGATGGGGCAGCAA[A/C]GCTGAAGAAATTGTT | 5607 |
rs542399851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712758 | TCCATCTCTACTAAA[A/G]ATACAAAAAATTAGC | 5607 |
rs542405701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661496 | ACTGAATACCAATAA[C/T]ATCCTTTAGATTTTC | 5607 |
rs542407662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671353 | GTTCTAGGTGCTTAA[C/T]GTATATAAATTATTT | 5607 |
rs542417270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766462 | TTATATTTTTGAAAT[A/G]TATTTCTCCATCTTG | 5607 |
rs542427983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560377 | TAAAACGACTAAGCA[C/T]AGATATTAAAGAGCA | 5607 |
rs542434671 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790871 | TGACTATGGAACTGC[C/T]TCTGGGCTGGGAATT | 5607 |
rs542469879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709182 | TCATTAAAGGTCATT[G/T]CCACATATGGGATTT | 5607 |
rs542471005 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670218 | GTGATTCCACTTATA[G/T]GACATTCTGGAAAAG | 5607 |
rs542489285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561128 | CTGGAATTTGTTTTT[A/C]TGCCAAGTTCAGAAC | 5607 |
rs542491970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608161 | AGAGATCTAATTTCC[A/G]TTTGAATCTATTCCC | 5607 |
rs542533047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567509 | AGCTGGGACTACAGG[C/T]GCCCGCCACCGCGCC | 5607 |
rs542548600 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603787 | TCTACACTAAGTTCA[C/T]CTTAATGGTGTTGAT | 5607 |
rs542555018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607442 | ATGGTTCTCTGTACC[C/T]TTCCCACCTTTGCTT | 5607 |
rs542559659 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755834 | GGGCTTTTTGCCAAG[A/G]AAGTCTGTTTCCATC | 5607 |
rs542569611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771800 | AGAGATTATAAGAAG[A/T]GTTTTCTTCTTGCTT | 5607 |
rs542580328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564835 | AGAGAACTGACATCA[A/G]TATACTTTCATTATG | 5607 |
rs542594167 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786665 | AGTGGTGGTACAACA[G/T]AAAGCCAGCTTCTCC | 5607 |
rs542612529 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729758 | AACAGAGCAAGATTC[C/T]GTCTCAAAAACAAAA | 5607 |
rs542614003 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799972 | ATTGTTATTGTGATG[C/G]TTTGGCTTCCTCTTG | 5607 |
rs542618696 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780160 | TCCATGTAGTACAGC[A/G/T]GCTCTCAACACTAGC | 5607 |
rs542621579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682448 | CAGGCTCATTTCGAT[C/T]TCCTGATCTCATGTT | 5607 |
rs542633608 | in-del | -/TC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575918 | CTTTCTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTT | 5607 |
rs542644956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635112 | CCCAGCCTTTGTTTT[A/G]TTATCATCCATTTTA | 5607 |
rs542654906 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804116 | CTCTGGGTGTAATGG[-/C]CCCAGGGTCTCCAGT | 5607 |
rs542658184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771355 | GTGCTAATCTTATCT[C/G]GCTGTGTGGTCTGAG | 5607 |
rs542679101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727438 | AAAACTTTAACAAAT[A/G]GATGAAAATAATGGC | 5607 |
rs542685615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673576 | TATGTTAGTGTGTGT[A/C]AAAGTTGGGATTTGG | 5607 |
rs542685919 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553636 | GAAATAGTTGAGGCC[A/G]GGCGTGGTGGCTCAC | 5607 |
rs542703320 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541080 | GACTTTTGATGAACG[G/T]TTTATTTTTCACAGA | 5607 |
rs542708555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628494 | AAAAAAAAATAAAAA[A/T]AAAAAATAAAAAAAA | 5607 |
rs542716046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711538 | TTAAAAGGAATTACC[A/G]TTTGAAATGTTTACA | 5607 |
rs542716150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577604 | TTTCTTTTCTTTTGG[C/T]TTTGGTCATTTCTGC | 5607 |
rs542724699 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551430 | CTTGAACTCCTGGGC[C/T]TACACAATCCTCCCA | 5607 |
rs542725129 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751682 | GCCTGTTGACGGAGT[A/G]TGGTGAATATCATTT | 5607 |
rs542726731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780689 | CCTCCTGCTAGGAGA[A/G]GTCATCTAGGTTAGA | 5607 |
rs542727039 | snp | C/G | 9.99883e-05 | 0.00706995 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772662 | TATAGCAAAAATATA[C/G]AAATGACACAGATAA | 5607 |
rs542759906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806101 | TGCACAGCCCAGCAC[A/G]TTCCTCCCCCTCCCC | 5607 |
rs542780132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628141 | GAGATTCTCAAAGAC[C/G]CGGTGCCCACTTAAC | 5607 |
rs542810613 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577754 | GCCTGTAATCCCAGC[A/G/T]CTTTGGGAGGCCAAG | 5607 |
rs542828653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648685 | CACCTCCTGGGTTCA[A/C]GCGATTCTCCTGCCT | 5607 |
rs542847793 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549084 | CGGCTTTGTCAGCCG[G/T]CTGCCTGGTGCCAGT | 5607 |
rs542852800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765652 | TCAAGGTCACTAAAC[A/G]TATTTATTGGCACAC | 5607 |
rs542853954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656273 | TTTTAAACTGCAAAA[A/C]GTTCACATGTGATTC | 5607 |
rs542875655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704436 | CTCTTTAAATAATAT[C/G]ATAGATAGAGTTGCA | 5607 |
rs542880894 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698333 | GCTGGGATTACAGGC[A/G]TGCACCACCACGCCC | 5607 |
rs542881984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756740 | CTACTTTGCTACTAT[A/G]AGTTCAGCTATTTTA | 5607 |
rs542892590 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557976 | ATGTAAGAGTTAATT[A/T]TGCATCCTAGAATTT | 5607 |
rs542893195 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660614 | GAAACAGAGAGTAGG[G/T]AAATAGGTGTATATT | 5607 |
rs542900585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802418 | TCTCCCCTGTGTCCC[A/G]CTTTTGGAGTCATCC | 5607 |
rs542930465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572605 | GTTTATGTATAGGAT[A/G]AAAAAGGATCATGGG | 5607 |
rs542945392 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658123 | AGCAACGTAGTGGTT[C/T]TCTGCATATATTCCA | 5607 |
rs542946281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801312 | AGTCACCTGATCACA[A/G]GGCTGCCCTGTCCCA | 5607 |
rs542948653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615249 | GTAATCTGCCCGCAT[C/T]GGCCTCCCAAAGTGC | 5607 |
rs542964491 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787895 | GCATGTGCTGGCAGA[A/C]CCTAGGACAAATAAA | 5607 |
rs542976724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592202 | AGAAAACACTTTAAT[A/G]CTTCCTAAATAACTC | 5607 |
rs542995542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570764 | AACTATGGACTGCAA[A/G]TAGTTGGTTAGTTTA | 5607 |
rs543003006 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770724 | ATGATCTGTCCGATG[A/T]TTATGCTAAAGGGAA | 5607 |
rs543008240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689827 | CTCTTAATTTCCAGG[C/G]AGCACCTTCTTCCAG | 5607 |
rs543013938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584507 | ATTTTAAGGAAAGAA[A/G]ATTTTGAGTCTTAAT | 5607 |
rs543027618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718437 | AACACGTGAGATGGG[A/G]TTTGGGGCAGTTAAC | 5607 |
rs543028158 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644744 | ATAAGATTTCTTCAA[A/G]CTTTAACTTTCTGTA | 5607 |
rs543034031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696436 | CTCATAACATGAAAA[A/C]TATTTACTAGCTGAC | 5607 |
rs543038104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591664 | ATGAGCCACCGCGCC[A/G]GCCCCTTAACAGGCT | 5607 |
rs543049602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740334 | AACAGAAATCCTGAG[A/G]CTCTAAATCAATTGT | 5607 |
rs543055090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563783 | ACACGATTTAAAGAT[A/G]TACTGTTGGTTATTT | 5607 |
rs543085915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747999 | TTTTCTCCCTATTCT[A/G]ATACAACCTGGAGGG | 5607 |
rs543099779 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611918 | TATCTTGTAGATGAC[C/G]AATATGAACAAACAG | 5607 |
rs543116763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627669 | GTCACCTTCAAAAAA[C/T]TCTTGTCAGTGATTG | 5607 |
rs543119072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613770 | TAGTGTGGACAATTT[A/C]TTGAGTTTTTAATGG | 5607 |
rs543124622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755975 | TTCCATTGTCCTCCC[C/T]ACATCCTCACTGTGG | 5607 |
rs543125905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733421 | AAAGATAAGAGAAAT[A/T]GTGAATAGTGATGTT | 5607 |
rs543174402 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639144 | GGATCTAATTAAACT[A/G]AAGAGCTGCACAGCA | 5607 |
rs543182322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634224 | TAAAAAATAAATTAG[C/T]TGGGCATGGTGGTGT | 5607 |
rs543183543 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612993 | TGTTCATTTAGCTGA[C/T]AGTTAAAAGAGGAGT | 5607 |
rs543193829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718796 | GGTACATAGTAAGTG[C/T]ACATGTGTATGGGGT | 5607 |
rs543195737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726665 | ATCTTAGGGTCAGTT[A/C]CTAGGCTTCCACTTA | 5607 |
rs543218921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772577 | TATATGCTAATACTT[C/T]GGCCAAGAATTGAAC | 5607 |
rs543223854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598847 | AGAATTTGTGTACTT[A/G]AGTGAGTGAAATGTC | 5607 |
rs543259337 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636208 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTAACA | 5607 |
rs543270860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733487 | AATTATTGCAGTATA[C/T]GGAGAAGATCACTTT | 5607 |
rs543293021 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559680 | CTAGCCAGTACATAG[C/G]CTTTCTGGTTCTACT | 5607 |
rs543297880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600250 | GGGGTCATCTGAGGA[C/G]TTTTCTAGGGCTGAT | 5607 |
rs543305726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786072 | AAGTGTTTGTAAACT[A/G]TGAAGTGCGAGACAT | 5607 |
rs543310525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741390 | AATTCATATTCGGTT[C/G]TCTCCTTAGTAGGCT | 5607 |
rs543314168 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547596 | GAGCAGCTGGGATTA[C/T]AGATACACACCACAC | 5607 |
rs543315267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578568 | ATAAAAAACAAAAAA[C/T]ACAACCTAACTACTC | 5607 |
rs543316133 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702873 | AAATTATTTTCAAAT[-/A]AAAAAATTAAAAGAA | 5607 |
rs543331487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765578 | ATTCCTTGAATATTA[A/G]AAGCATTTTTCTCAT | 5607 |
rs543338536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793071 | AATTACAAGCAAGAG[A/G]TCTTAAATGTGTTAT | 5607 |
rs543351654 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731031 | ATATGAAACCACTCT[A/G]AAAAGTACAAAGGGC | 5607 |
rs543354274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621911 | GAAAGTGGCCGGGTG[C/T]GGTGGCTTACGCCTG | 5607 |
rs543381125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672933 | AATCCTTTCCCTATT[A/G]CTTGTTTTTGTCAGG | 5607 |
rs543396436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633472 | AGACTAATATTAAAA[A/G]TATTGTGCATTAGTT | 5607 |
rs543401311 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569030 | AAAAACAAAAAAAAA[A/C]AACAAAACTCTGTGG | 5607 |
rs543438078 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695661 | ACCCAGCATGTTCTT[A/G]GTAGCTTTAAATTCC | 5607 |
rs543438639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640949 | GATAACTATTTCATA[A/T]TGACCATGTGTAATT | 5607 |
rs543441477 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739335 | CAGTTCATTCTTGAT[A/C]CATGACTTATTTTGT | 5607 |
rs543468874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710234 | TCATTCTTTCTGCCT[A/G]TTTGCCACCCCTCTA | 5607 |
rs543506092 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548316 | TTTAAACCTACACTG[C/G]CTAGAATGAGTGTTC | 5607 |
rs543521723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673413 | AGTATAAATTTTAAG[A/T]TTAAAAATGTTATAA | 5607 |
rs543536089 | in-del | -/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547456 | GGTTTTCTTTTTTCT[-/T]TTTTTTTTTTTTTTT | 5607 |
rs543577844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710311 | TTGGTTAATTGGTGC[A/G]TCATCTAGTCCTCGG | 5607 |
rs543581256 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699051 | AAGGCAATTTAATGA[A/G]GACATCAGCTTCTAG | 5607 |
rs543594069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571634 | TTTTAAGAAGGTTTC[C/T]CATATACCAGCTCCT | 5607 |
rs543611629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675518 | ATGTTCTCCATCTTG[A/G]CTATCAGTGTCAATA | 5607 |
rs543615537 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665105 | CAGGTTGTTGTTAAA[C/T]CCCTAGCCTCAAGCA | 5607 |
rs543627379 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665671 | GATTTTGACAAATCA[A/T]ATAGTCAGGTTTTTG | 5607 |
rs543634287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683143 | CAAAAACTCTGTCTC[A/C]AAAAAAAAAAGTTGT | 5607 |
rs543637041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655331 | TGAGTTACTGTCTTT[C/T]AACTTCAATCTAAAG | 5607 |
rs543657309 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593806 | TTCCCGTCCATGTTT[C/T]GAAGGCTGAAATCTT | 5607 |
rs543658657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562498 | TGGCCTCTGATGATA[C/T]TTACTCAAATTTACA | 5607 |
rs543662708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569808 | CATTTTGTCATTTAT[A/G]TGGCTCTGCTCCCAG | 5607 |
rs543672001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710689 | TTGTATTTTTAGTAG[A/G]GATGGGGTTTCGCCA | 5607 |
rs543694154 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547408 | GAAGAAGAAAAGTAT[A/C]AAAAAATGGTCATCA | 5607 |
rs543700152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704083 | GCTCCATTAGAACTC[C/T]ATGCTATGTTTTTTT | 5607 |
rs543702795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67664017 | TTATGAATTCAGCAT[A/G]GGTACTTCCAGATTA | 5607 |
rs543708747 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653187 | CTGCAAAGTTGGTAG[C/G/T]AATGTTCCCTCTTCC | 5607 |
rs543710957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800604 | ACAGCAATGACCAAT[C/T]GTTCATATGAATCGT | 5607 |
rs543711587 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752671 | TGACAGAGCAAGACA[A/C]CCTCTCAAAAAAAAA | 5607 |
rs543726229 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745404 | TCCACTTTTAATGTG[C/G]TATAAACTAGGGGCT | 5607 |
rs543729007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647981 | GGAGATTAAGCCTGT[A/G]GTGAGCTGTGATCGT | 5607 |
rs543734969 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618021 | CTTTAAAGATTATTC[C/T]AGAAATTCAGTTTAT | 5607 |
rs543737131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703545 | AGAGTTTGACCATAA[A/G]GTCTTTGATTCCTTG | 5607 |
rs543751206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666010 | AATTAACCCAATGGT[C/T]AGTTCTCAAAATTTT | 5607 |
rs543759585 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597114 | GCGGAGCTTGCAGTG[-/A]GCCGAGATCACGTCA | 5607 |
rs543795191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566221 | ATTCTGTTGCCTAGG[A/G]TGGAGTGCAGTAGCC | 5607 |
rs543804587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778013 | TCAGAATAGCGCTCT[G/T]GGATTTTTTTCCTTC | 5607 |
rs543808365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605653 | CAAAGCCAGATTTCT[A/C]TACAGCATTTCTTTT | 5607 |
rs543838573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677339 | TAAAATGGGGTTAAT[A/G]ATAGTACCTATCTCA | 5607 |
rs543843455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625988 | GCTGGTCTCAAACGT[C/T]CAGGTGTTGCTTATT | 5607 |
rs543864685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576085 | CCACGCCTGGCTAAT[A/T]TTTATATTTTTAGTA | 5607 |
rs543868580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774315 | AATACAATGAAAAAT[A/G]TTGTCACAGGAAGCA | 5607 |
rs543887622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718993 | TGCCATGAATTACTA[A/G]AATTTTATTCATTCT | 5607 |
rs543906757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620274 | TATTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 5607 |
rs543912875 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664980 | TACATCCTTCCTTCT[A/G]TTAACATTTCAGATA | 5607 |
rs543931382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706919 | AGAAACCCAAGGTTC[C/T]TGTGTTTTCTTTTTG | 5607 |
rs543933385 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572710 | TTATTATTATTATTT[A/T]TTTTTTTGAGATGGA | 5607 |
rs543960008 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600617 | TGTTTATGGCCCAGA[A/G]TTGCTTTTCCTTGAC | 5607 |
rs543975164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725043 | GTAGGACTGAGGTTC[C/T]ACAAGATGTCAGGAA | 5607 |
rs544009622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605240 | TCTGTATTTTAGTAG[C/G]GATGGGGTTTCACCA | 5607 |
rs544025295 | in-del | -/TAAG | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721065 | TGCCCTCTTCCTGTT[-/TAAG]TGTCTACTGTAATAA | 5607 |
rs544040019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612836 | GCATTTACATGGTGT[A/G]ATTTCCCTAAATTGC | 5607 |
rs544043589 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654642 | TTTCAAAGGTACCAT[A/T]TAAATTCCCCATGGT | 5607 |
rs544047734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792140 | TGCAAAAGGAGGTTA[A/C]GATCAAAGGAACTGT | 5607 |
rs544053653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566740 | TCTGGCTTTGGGCCA[A/G]TACAAGTGTACATTT | 5607 |
rs544080152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693063 | CTCCCAGCCAAACAC[C/G]AAGACCAAAGCGAAG | 5607 |
rs544082504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590923 | GGAGTATATAGAATA[C/T]GTAAGATGTGTCTGT | 5607 |
rs544088669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648566 | TTTTGTGTGGACATA[C/T]GTTTTCAGTTCTTTT | 5607 |
rs544089330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602322 | TTCCCTGGAGGGAGC[A/G]CTTTTCAAAGCTTGA | 5607 |
rs544114168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554363 | CGCACCTGGCCTTAT[A/G]GTAATACATTTAATA | 5607 |
rs544127919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651460 | TTGTGGTGCCAAACA[C/T]TGGATCTTATTCTTT | 5607 |
rs544137755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804388 | TCGCTTCCCTTGCAG[A/G]TGGGGTAAAGTATCG | 5607 |
rs544147717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647853 | CACCCTGGGTGACAA[A/C]GTGAGACTCTGTCTT | 5607 |
rs544158453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758630 | TTTTCAAGACCTCAG[A/G]AATACAAATCCAAAA | 5607 |
rs544158506 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574895 | AAAAATAAAACAAAA[C/T]AAAATAAAATTTAGT | 5607 |
rs544160098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749209 | TTGAATTCCACTGTT[A/C]CTTTGCCTTCATGGT | 5607 |
rs544160912 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775107 | AGAGTGGGCACTTAG[A/G]TGGTGAGGTCACTGT | 5607 |
rs544170928 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599443 | GTTTCTGTTACCTGC[A/G]TTGTACTCCTAATTA | 5607 |
rs544195833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550711 | GATGCTGAGAGGGAT[A/G]AAGTAAGAACTGTAG | 5607 |
rs544210195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721039 | AGGATATTGTACTTG[C/T]GAATTACTGTTGCCC | 5607 |
rs544245462 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757709 | GTAATGTAAGTGATA[C/G/T]GAGACTTGATGGCCT | 5607 |
rs544259421 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641370 | AAGACAATTATGTCG[C/T]CATAGATTAAATAAG | 5607 |
rs544260303 | snp | A/C | 0.000585122 | 0.0170944 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642461 | TGTACATATTGAGGG[A/C]CAGAGCTAGAGATGA | 5607 |
rs544260800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549426 | TAAATGTGGCATAAT[G/T]GGTTTATATCGTCAT | 5607 |
rs544265096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649731 | TATTTGATTACTTGT[A/G]CTTGAAAACTCTGGA | 5607 |
rs544293868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607257 | GATTGCATTATAGTA[C/T]CGTGACAAGCAAGGA | 5607 |
rs544300618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609026 | ATTGCTGGGTGACTC[C/T]GGGAAGTGGTGAACT | 5607 |
rs544304770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616895 | ACTCTATAAATAATT[C/T]ACAGAGTAATTGTGT | 5607 |
rs544320390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573379 | CTTTCTTCACAGGGT[A/G]GCAGGAGAGACAGTT | 5607 |
rs544323667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641975 | GAATAGAGTTATTTT[A/G]AGGTGGGTTCTACTT | 5607 |
rs544327305 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690658 | CCTCCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 5607 |
rs544330744 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657177 | GGTGGTAAGGTAATC[A/T]TTGTTTTTTAGGTTT | 5607 |
rs544349909 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626838 | CCGGGAGTTCAAGGT[C/T]ACAATGAACTAATAA | 5607 |
rs544367012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616206 | CAAAGAAGCATCATC[G/T]GTAAGAATAGAAGCA | 5607 |
rs544367343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721474 | ACAAGCTCTCAGACT[A/G]CTTGGCACTTTTCGT | 5607 |
rs544374550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551519 | TAAATTTTATGTGGA[A/G]ATGGGGTCTTGCTAT | 5607 |
rs544392099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635770 | CTGTTTTCTTTCAGT[C/T]TTTTAAAGATTTTGT | 5607 |
rs544393642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661569 | TTTCTAAAGGAAAAT[A/G]TAGTGTATTTTGACA | 5607 |
rs544395348 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776956 | AGGAAGTCAGAACCC[C/T]AGAAATTACATCCGA | 5607 |
rs544432014 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624333 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 5607 |
rs544432362 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609602 | AGATTCTGTAGACCT[A/T]TTCTATAGGTCTGTA | 5607 |
rs544444316 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790945 | TACAGAAGACGAGTC[-/AG]AGCTAGGGGGAATAA | 5607 |
rs544454814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656587 | TCCCTCCTTGGCCTC[C/G]CAAAGTGCTGGGATT | 5607 |
rs544460860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760195 | TAGAAATGACATTAA[C/T]ATTCTACCAAAACAC | 5607 |
rs544470752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637201 | GCTTGCAGATGGCCT[A/G]TTGTGGGACTTCACC | 5607 |
rs544479137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644533 | ATTCTAGATAAGTTT[A/G]TAAATATTTTATATT | 5607 |
rs544492713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797751 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAACCT | 5607 |
rs544494075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781581 | CCGAGAGACATTTGC[C/T]GGAGTGTGGACTAGT | 5607 |
rs544494123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676459 | TTTGCCAAGCAGAAT[A/G]GACAGACAGCTTTAG | 5607 |
rs544496647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691627 | ATAAAAGACGCATTG[A/T]AGCAGATGCTGCTCT | 5607 |
rs544504668 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696263 | AATTTACTGGAACAA[C/T]GTACTGATCACTCTT | 5607 |
rs544511030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742116 | AGCCAGGATGGTCAT[A/G]ATCTGCCCTCGTGAT | 5607 |
rs544517934 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653831 | AAATTTTCCTCTAAG[A/C]ACGGCTTTAGTTGCA | 5607 |
rs544532728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636365 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 5607 |
rs544543284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622824 | AGTGTATGGGCTGGG[C/T]GTGGTGGCTTACGCC | 5607 |
rs544548154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608095 | TCCCCAGCAAAAGTG[A/G]TTGTGATCAGGTAAA | 5607 |
rs544577694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676339 | GAATCATAATTTTCT[A/G]AGGGCAGTGTTTTTC | 5607 |
rs544580732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657923 | ACCTTATGAGGCATA[C/G]TTATGAATCATCCAG | 5607 |
rs544587680 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602241 | TCTGAAGGTACTTAA[C/G]TTCAGGTACCCATAG | 5607 |
rs544593479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557903 | TTTTAAGTAAAACTA[A/G]GTAAGTTAGTGAAAA | 5607 |
rs544598205 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572704 | TTGATATTATTATTA[C/T]TATTTTTTTTTTTGA | 5607 |
rs544606663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628693 | GAATGGCCACAACGG[G/T]GAAGTTAGGAAAGCC | 5607 |
rs544613683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713324 | TTACATACACATATT[A/G]TTTAATGGATGCCAG | 5607 |
rs544637977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549930 | ATAGTTTATGCTAAC[G/T]TTTCAAAAATCTTTC | 5607 |
rs544638350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705477 | CAGTGGCTCATGCCC[A/G]TAATCCCAACACTTT | 5607 |
rs544644366 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666557 | TGACCAGAGACTCTC[A/G]GAAGCCAGTAGGTCC | 5607 |
rs544667321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564742 | AGATTGGCTAACTCT[C/T]CTGAGAATGTGACAT | 5607 |
rs544683017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601132 | GTGGAAGCCAGACCT[A/T]ATAAATACCATTGCT | 5607 |
rs544692147 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741751 | GAAGAAAACAGGGAT[A/G]TTCATTCAAGAAAGA | 5607 |
rs544699672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698204 | TCTTTATTTTTTTTT[C/T]CTTGAGATGAAGTCT | 5607 |
rs544700044 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628128 | GCTGTCTCAAGAGGA[C/G]ATTCTCAAAGACCCG | 5607 |
rs544706039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593234 | TAATCAGTTCTGAAC[A/G]AGTGTGTCAACTCGT | 5607 |
rs544707338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699569 | ACGTGTCCTAGGTTG[A/G]ACAAGGCACATCATG | 5607 |
rs544715651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650510 | TTCTATTTCTAGTTT[A/G]TTGAGTTTTTTTTTT | 5607 |
rs544748603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692278 | GTAGAAACCAGAAAT[C/G]GTTGAACGTGGAGGA | 5607 |
rs544749010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705956 | AAATTTAGAGAGGTA[A/G]CCAGGGGCCAGGGCA | 5607 |
rs544755439 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707076 | GCGTGCCACCATGCC[C/T]GGATAATTTTTTGTA | 5607 |
rs544755472 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556246 | CTTATTGCTCTTTTC[A/G]GTTTGTTCTGGTCTT | 5607 |
rs544759985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697361 | TAATATTATTATTCT[C/G]ATTTTAGAGATAAAG | 5607 |
rs544767628 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703020 | TTCAAGTCTCAGCTC[A/G]TTCACTACTTAGGAC | 5607 |
rs544778806 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587577 | CACTTTATCAGCCAA[C/T]GCAGCTCCTTCCCTT | 5607 |
rs544805134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795658 | TTTTTCCCCCCAGTG[C/T]TCTCTCTTTGCTTGA | 5607 |
rs544810284 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687351 | GAGCTATTTATTTGC[A/G]TAACTTTCATTGTCT | 5607 |
rs544820812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714108 | GGCAAACAAAATAGG[C/T]ATATTCCCTTTCCTT | 5607 |
rs544846324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593737 | TGTATTGACTGAGAC[A/T]TCTGTGTCACTGCAA | 5607 |
rs544856473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628998 | TCAAATTTCAGACCC[A/G]TGAAGGGAGGAAACT | 5607 |
rs544858026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573310 | CAGTTCTGCATGGCT[G/T]GGGAGGCCTCAGGAA | 5607 |
rs544884862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684635 | CTGTAGAAATAGATG[C/T]CCCCCTCCCACACAC | 5607 |
rs544887236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608408 | TGCTGTGTGGAGGGC[G/T]TGTCAGATGTTGGGG | 5607 |
rs544892191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707248 | AGGGTCAATATAATG[A/C]GAACATTACCTGAAG | 5607 |
rs544893300 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542086 | GGAACTGTTTGCTAT[C/T]TTAGGGCACTCGTGC | 5607 |
rs544958586 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699079 | TAGTTTCTGCTAATA[G/T]CAGACTAAGTTATTT | 5607 |
rs544960468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578042 | TGCAGTTTATTACTT[A/G]CTGTCTTCTCTGTTT | 5607 |
rs544963444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765497 | CGGGGAGTTGCAGGG[C/T]GGAGGGTAGATTAAT | 5607 |
rs544966694 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576929 | ACCCTATATATATAT[-/A]TTTTTTTTTTTTTTT | 5607 |
rs544969558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656386 | ATGTAGTGCAGTGGC[A/G]CAGTCTCTGCTCACT | 5607 |
rs544992956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558104 | TTTCTTATTAATAGT[C/T]TTGCTAATTTGTATG | 5607 |
rs545007665 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561053 | CTTTTTAACCATAAT[C/G]TCTATAGCTAGCTTA | 5607 |
rs545013497 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793837 | AGGTGGACTTCAAAC[C/T]GTTGAGGTTTTATTT | 5607 |
rs545018242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628678 | AAATAACCATACTGT[A/G]AATGGCCACAACGGT | 5607 |
rs545037592 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776678 | TTCAATTTCTGTGTT[G/T]AAATATTTTTAAATA | 5607 |
rs545066559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774238 | ATATATCTCTTTACA[A/G]CTCTATACCCTGTTG | 5607 |
rs545085223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613837 | CATCTGATATTACGG[C/G]GAAGAAGGGAAGAAA | 5607 |
rs545094118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623202 | AATGAAAACTTGGCC[G/T]TCTCATGATTGTTTA | 5607 |
rs545100395 | in-del | -/TGTT | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786060 | TGGAGGTTATGAAAG[-/TGTT]TGTAAACTATGAAGT | 5607 |
rs545100697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665042 | CACATACTGGAAAGA[A/G]AAACTTTATTTTTAA | 5607 |
rs545127326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801399 | AGTCCTTGGCCTCCT[A/G]TCCCATGCAGCATCC | 5607 |
rs545127584 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728505 | ATTAAAATTTCTTTA[A/G]GATTTTTATTATAGA | 5607 |
rs545131711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728139 | CTGATTTTTTCTTCT[C/T]GTTAAAGGTTGAGAG | 5607 |
rs545147688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803657 | TATTTTCCCTGAATC[C/T]CATGCAGGGCTGATG | 5607 |
rs545152019 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767471 | CAGTACTACACCCTC[-/A]AAAAAAAATCCATGA | 5607 |
rs545212808 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67807060 | GTTTTTCTCTATAAA[C/G]GGTCAGGCCCGTCAG | 5607 |
rs545231277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690565 | TTTGAGACAAGTCTC[G/T]CTCTGATACCCAGGC | 5607 |
rs545234132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667766 | ATTTCTCGCATTTAT[A/G]TGGCTTCCTTGGAAT | 5607 |
rs545240426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649546 | ATTTATTCGTTTGCA[G/T]GTAGATATACATTTG | 5607 |
rs545242285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803713 | CCAGTGTGTCCAGGG[A/G]ACAGTGCTGATAGAG | 5607 |
rs545263282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767029 | TCTTTCCAGGGACCA[C/G]TGAGATGAGAATCTG | 5607 |
rs545268876 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795874 | TCCTGTCCATTTTTG[-/C]TTTATATGTTTTAAG | 5607 |
rs545275613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795807 | CAATTTCTAAGAGAG[A/G]TATGCTAAAATCTCC | 5607 |
rs545279927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643498 | GTTGCCCAGACTGGT[A/G]TGCAGTGGCGTGATC | 5607 |
rs545284265 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641038 | GCAGATAAGTAGAGC[A/G]GAAAACAAATAAAAA | 5607 |
rs545289370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787065 | CTGTGCACACCAGAG[A/G]GTAGTGGGGCAGTTG | 5607 |
rs545296497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697306 | AATCACTCTTCTTAC[A/G]TATATTAACTTTTAA | 5607 |
rs545316236 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733111 | TAGAAAAGAGCCTTT[-/A]ATTTCATTTCACCCC | 5607 |
rs545336598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756808 | TTTCTGTGTCTGACT[G/T]ACTTCACTTAGCATA | 5607 |
rs545341843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651401 | AATTCCACTTGTGTA[G/T]TTATTTTGAAATATA | 5607 |
rs545345263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761863 | TAATCAGCACTTCTG[C/T]AGAACCAGCTGAAAT | 5607 |
rs545347644 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760041 | TGTAAGGCAATCTTT[A/G]GAAATCTAATACCTT | 5607 |
rs545361048 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656124 | ACAAACCAGTAACTT[G/T]GGAATCACGAGCAAA | 5607 |
rs545365930 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594881 | TCCTTAATTCCTCAG[-/T]TGCTATAGGATAACT | 5607 |
rs545369352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564562 | AGGATGATTAACAGA[A/G]CATTGCATTCCAACC | 5607 |
rs545374914 | in-del | -/TTAA | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781751 | TAACCCGATTGACTC[-/TTAA]TTGTTAGCCTGTGTG | 5607 |
rs545377985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653036 | ATCTCTTTATATACT[A/G]GTTTAGTCAGATTTT | 5607 |
rs545414510 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632079 | TGAGTGACTACTATA[G/T]GCCAAGTATTATGCT | 5607 |
rs545431487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556568 | TCTTTTTTTTTTTTT[A/T]TGAGATGGAGTCTTG | 5607 |
rs545433463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711670 | ACACACAGGCGTGCA[C/T]GCACACACACACACA | 5607 |
rs545443177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752693 | AAAAAAAAAAAAAGA[A/G]AAAGAAAGAAAGAAA | 5607 |
rs545450316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645765 | GCTATGGTGCTTAGA[C/G]TGGCCATATACCCCT | 5607 |
rs545457533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804538 | TCGCCTACCGGGGCA[C/T]TTGGGCAAACTGCCT | 5607 |
rs545461581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561007 | CCTTATTCAGGTCTT[A/G]GGTATATTGAAATTC | 5607 |
rs545500132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716334 | AGCAAGACTCTGACT[C/T]TAAAAATAAAAAAGA | 5607 |
rs545503342 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587466 | GGCGAATGAGCAGAA[A/G]CTCCCATCTAATCCT | 5607 |
rs545514852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645038 | CTGTAATCCCAGCTA[C/G]TCAGGAGGCTGAGAC | 5607 |
rs545515070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653765 | CTTCTGTTTAAGGTA[A/G]CAAGTTAGGATATTG | 5607 |
rs545520539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553346 | CCTCTACTACTCCAG[G/T]TTTACGTTCTGTGAT | 5607 |
rs545532931 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648704 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 5607 |
rs545534190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614434 | ATTAGATGGTTATCA[C/T]GTTGTTTCAAGAGAG | 5607 |
rs545546102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704681 | CAGCTGAGAGGTTAG[C/T]GATAATGGTGGTCAG | 5607 |
rs545567901 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557925 | TAGTGAAAAATGGTC[A/G]CAACAAACCTACACT | 5607 |
rs545571387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750206 | TGTAACTTAAATGAT[A/G]TATTTTTCTTCATAG | 5607 |
rs545578609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593007 | TTAAGATTTTCACAT[A/G]ATAATAACATATTAC | 5607 |
rs545591906 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720663 | CGGATGAGCCCCGTC[A/G]GAAGAGCTGAAAATG | 5607 |
rs545594315 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685671 | GAAAATGGAAATATA[G/T]TATTGTAAGGTTTGT | 5607 |
rs545606880 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790651 | CTTACTGAGTGGTGA[C/G]GGTCTTTAAGATGTG | 5607 |
rs545639054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695051 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 5607 |
rs545640880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635639 | TTCCTTTACATTTCA[A/T]ATAGTGTGGGTCTTT | 5607 |
rs545653930 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636388 | ACTCCAGCCTGGGCA[A/G]CAGAATAAGACTCCG | 5607 |
rs545681621 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637849 | CTCATCTCATTTGTT[G/T]TCCATCTTTCAGGGA | 5607 |
rs545692475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799028 | ACAAAAATTAGCTGG[G/T]CATGGTGGCGGACAC | 5607 |
rs545698036 | in-del | -/A | 0.0341408 | 0.126114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674474 | TATGTTTTTGAAAAG[-/A]AAAAAAAAGACTTAG | 5607 |
rs545700174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642397 | CATAGCCACTCTAAT[A/C]TTGAGGCTTCTGTTT | 5607 |
rs545709783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593688 | GCCTTGGAGGCAGGC[A/G]CCTGTCCATTGCGAT | 5607 |
rs545717340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791061 | GCCATGAATAGTCCA[C/G]CTGTGAGACATCCGA | 5607 |
rs545717834 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734340 | ATATTTTGTTTAACT[A/C/T]GGCTTGGAAACGTGC | 5607 |
rs545723625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639371 | GATTTATACAATGCT[A/G]AGCATTTTGCATGCA | 5607 |
rs545747596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632378 | GTCCTGGGATTATAG[A/G]CATGAGCCACCACGC | 5607 |
rs545761045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552587 | CTACAGGCACCCACC[C/T]CCACACCTAGCTAAT | 5607 |
rs545768939 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806507 | TCTAGGCCGTGAAAT[A/G]GAGCTGATAGCCTCC | 5607 |
rs545793993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610320 | TTGGTCTACCCTTTG[A/G]GTGTCCTTATTTACC | 5607 |
rs545813207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602655 | AACATAGGCTTGTTT[A/G]TTTGTTGGTTGGTTT | 5607 |
rs545828672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661420 | GAGCGAGTGATTGAC[A/G]ACAGATATAAGTACT | 5607 |
rs545833594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708544 | ATGTTGCCCAGTGTT[A/G]CCTCGAATTCCTGGG | 5607 |
rs545858758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736665 | ATATACAGAATCTCG[C/T]CATTTTTAGTTCAGT | 5607 |
rs545870498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567413 | CCCAGGCCGGACTGC[A/G]GACTGCAGTGGCGCA | 5607 |
rs545883601 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690973 | TTGGGGCGATGATAC[C/T]GATAAAAAGAGCTTA | 5607 |
rs545885636 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725213 | GCATTGTCTTACAGA[A/G]CAAACAAATAACATC | 5607 |
rs545900362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560329 | TACTTTTCTAACTCA[A/G]TTTCCTCTTGGACAA | 5607 |
rs545942907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687279 | GGTTTCTGGTTCAAT[A/G]AGTCTGGAGTAGAAC | 5607 |
rs545944023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709150 | TGTAGTTCCCCTCCT[A/G]TGGATTAGTTATGGA | 5607 |
rs545970041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782481 | GCTAAATATTTCATA[C/G]AGCCTGATTTTAGTT | 5607 |
rs545973396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638762 | TTTTTAGTAATAGCC[A/G]TTCTGACTGATGTGA | 5607 |
rs545982224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623887 | CAGGTGTGAGCCACC[A/G]CCCCCGGCTACTTCC | 5607 |
rs546008036 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683143 | CAAAAACTCTGTCTC[-/A]AAAAAAAAAAGTTGT | 5607 |
rs546016271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745435 | TCACTTTTTCATGAA[C/T]TGTGTGCAAAAGCAG | 5607 |
rs546042394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597381 | CCATTGATAGGAATG[C/T]CCCTCCATACTTAAT | 5607 |
rs546047753 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755320 | TAAAGTAGGCTCTTC[C/G]CTTATTTTTCTCCTC | 5607 |
rs546049898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668778 | AAAATAAAATTGGCA[A/G]TCATTCTGGGGCCAT | 5607 |
rs546075007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630264 | CAATCAGATAAACAC[A/C]AAAGGTCTTGATGGA | 5607 |
rs546088643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625269 | AAAACTTACACCAGG[C/T]GACTAACTTTTGCCA | 5607 |
rs546108333 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631432 | TCGGTCTTTTCTTTT[C/T]CTATGCACCTTTTAC | 5607 |
rs546117241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590878 | GCATATGCCAAGTCA[C/T]TGGGCTATATTTAAG | 5607 |
rs546122821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624231 | GTAGTCTTAGCTACT[C/T]GGGAGGCTGAGGCAG | 5607 |
rs546122905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617086 | AAGTCATTATACATG[C/T]AATTACGCTCCAGGT | 5607 |
rs546125505 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749682 | CTGCAAGCCATAATC[C/T]ATGTTGATGTAAAAA | 5607 |
rs546129734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730748 | CAGTGCCAGGGAATT[A/G]CTGCTGTGAACCTAA | 5607 |
rs546138990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692914 | AATTAATATTGGGAG[C/T]AACAATGGTGGAGGG | 5607 |
rs546154321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651537 | TTCCTTTCTCACTAC[C/G]CTTCTCAGTCTCTGG | 5607 |
rs546155997 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598767 | TGTGGCCCCTCCAGA[-/GT]GTGTAGACTCTATCT | 5607 |
rs546192507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543824 | TGGACAGATTCCAGC[C/T]TTGTTTTTCTACTGA | 5607 |
rs546200358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699810 | AAGTCCTAAACAAAA[C/T]TTCTAGATTAAAATT | 5607 |
rs546200520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643918 | TTTTTTCTTCAGTAT[A/G]ATTGTATATATATTC | 5607 |
rs546209679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582846 | CACACACACACACAC[A/G]CACACACACTTCCAA | 5607 |
rs546236482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629533 | ATGATGTTTCCATGT[G/T]GGCAGTAGTGGATTA | 5607 |
rs546237477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796650 | TCAAATATCCAAACT[A/G]TTTAACATATCCGGT | 5607 |
rs546243340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797022 | GAGTGCTGTTGCTCT[G/T]CTAGGTGACAGTGTT | 5607 |
rs546246296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642949 | TAATAGTCATATATC[C/T]TAGCACTGAATAAAT | 5607 |
rs546255391 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585178 | CTATAGTTTTCAAAT[A/T]GAAGCAGTCTATAAC | 5607 |
rs546262012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652002 | TATGAAGGTTCCCCT[C/T]TCTCCACATCCTTGC | 5607 |
rs546262752 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542610 | GAGCTGCTGCCCTTT[C/T]CCAACATGGCGCCGC | 5607 |
rs546276008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692683 | CTTTTCCTCATCTGG[A/G]AGTGTGTTATTCATT | 5607 |
rs546289235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698498 | CTCAGCCCAGAAATT[C/T]TAATTACTAAAAATT | 5607 |
rs546312518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550203 | GACCATCATATGGTA[C/T]ATTTAAATATTTATA | 5607 |
rs546312951 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789690 | ATTGCACTCCAGCCT[C/G]AGCAACAAGAGCAAA | 5607 |
rs546319061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685366 | ATACATTTTCCAAAA[A/G]TAAACAGCTAAATAA | 5607 |
rs546330797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796291 | CATTCTTGCATTGCT[A/G]CAAAGAAACACCTGA | 5607 |
rs546350098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788935 | CATGATTGTACCATT[A/G]CACTCCAGCATGGGT | 5607 |
rs546383330 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617732 | GGCCTCACTCTGTCA[C/T]CTAGGCTGGAGTGCA | 5607 |
rs546394595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582552 | AGGCAGGGCACAGTG[A/G]TTCATGCCTGTAATC | 5607 |
rs546411065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574854 | CCTGGGCGACAGAGT[A/G]AGACTCCATCTCAAA | 5607 |
rs546424156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594439 | CTGGAAAATATATTT[A/C]AAAATTGACATAAAT | 5607 |
rs546436243 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756461 | TTGATAAACATATAC[A/G]TTGTGAAAGGATTAC | 5607 |
rs546442825 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582338 | GTGCTGGGATTACAG[G/T]CGTGAGCCACCACGC | 5607 |
rs546487293 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805879 | CTGCTTTTTTCTGAC[C/T]TTCCCTGGGAATTCC | 5607 |
rs546491683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782200 | GTCTCCCGCCTCTGC[A/G]GTTTCAATAATTTTA | 5607 |
rs546497542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596062 | TATAAATCTACTCAG[A/T]TCAGATCTAGAACTA | 5607 |
rs546500752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543979 | GCTGTGGCACGATCT[C/T]GGCTCACTGCAGCCT | 5607 |
rs546501458 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785256 | GGCCCCGAACTGTTT[C/T]TTAAACACAGGAAGA | 5607 |
rs546516288 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781265 | ATCAATTATTAACCA[A/G]TCTAACCAGGAATTT | 5607 |
rs546516726 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582171 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 5607 |
rs546518232 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644102 | CACTGCCTTTTAAAA[C/G]TAAAAAACAAGCTGG | 5607 |
rs546574199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635306 | CAGCCTCCCGAGTAG[C/G]TGGGACTACAGGCGC | 5607 |
rs546588216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707001 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 5607 |
rs546619235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741689 | AGTATCCTTAGTAAT[A/G]AAGGGGAGAAGGATA | 5607 |
rs546625788 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619507 | ATATATCATATACTG[-/T]TGGAAGAGGTCAAGC | 5607 |
rs546625822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601724 | ATTGCCCTATTCTAT[C/G]ACCATGAAGGTTCAC | 5607 |
rs546635608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634760 | TGACAAGTGTTAGCA[A/T]GATATTTTTTTTTTT | 5607 |
rs546649651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628809 | TTTTTAGTGGGAATG[A/G]CAATTTTGGTCATGG | 5607 |
rs546657346 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545092 | TGATTTTCATTTCTC[C/T]CAGGTGTCCAGGCTG | 5607 |
rs546657408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595418 | TCTGAAACCATTATT[A/G]CTTCGATTTGTGAAG | 5607 |
rs546684387 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606360 | TCCAGCTCCTTCCCA[C/T]AGGATAGAGTAAGAG | 5607 |
rs546688574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773082 | AAGATCATCAGTGCA[A/G]TAAGTTTTTAGTGCA | 5607 |
rs546711252 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673760 | TTTTTTTGCAGAGAT[-/C]TACATAGTTTGTGAT | 5607 |
rs546713128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628377 | CCCAGCTACTCGGGA[G/T]GCTGAGGCAGGAGCA | 5607 |
rs546721101 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758751 | TTACACAGTGTTTCC[C/T]GTCACATTCTTTCCC | 5607 |
rs546733520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743307 | TAAATCTTCCTGTGA[C/T]TTTTTTAGGTCCTGT | 5607 |
rs546755361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675961 | ACAAATGCAAATGGA[A/G]GAGGATAGTTATTTC | 5607 |
rs546764187 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723381 | TGGTTGGCCAAGTCA[A/G]AGGTCAATAAGATGA | 5607 |
rs546764207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602414 | GCAACTCTTTGTATT[A/C]CTTTTATTTGCTTCA | 5607 |
rs546779573 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727100 | GCTACCTTGGGAGGC[G/T]GAGACAAGAGAATCA | 5607 |
rs546789418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789163 | GTGAGTCATTGAGGT[C/T]TTTCCATATAATATA | 5607 |
rs546805389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736205 | AGATAAAGAAATTGG[C/G]TTTGAGAATTTTGTA | 5607 |
rs546806746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666364 | ACCTTTTGTATTCCT[G/T]TATCTAAATTTTTTT | 5607 |
rs546818530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683625 | AAATTAACTGGGCTT[A/G]TTGGTGGGCGCCTGT | 5607 |
rs546842305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722178 | TCTCTGTTACTCGCA[C/T]TTATGCCCCTCCACA | 5607 |
rs546843934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743899 | CTGAAGGGAGGGGGC[C/T]TCTGGGGACCATGGG | 5607 |
rs546844466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802777 | TTCCAGGGAGCTGCA[C/T]CATGCCGCGCTTCCA | 5607 |
rs546855794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802588 | CTCACTGCCTGGTGA[A/T]GAGGCCAGCAAGATC | 5607 |
rs546870980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678783 | AGCCTGGCCAATATG[A/G]AGAAACCCCATCTCT | 5607 |
rs546874462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624080 | CGCAGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 5607 |
rs546877802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614944 | AAATTAATATCTGTG[A/G]CCTCATAACATATTT | 5607 |
rs546933140 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628290 | TTTGAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 5607 |
rs546942877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551792 | GTAAACTAAATGCCT[A/G]TTATAATGGATTAAT | 5607 |
rs546972678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587325 | CAGGACTTATCATGC[A/G]GGGCCTCGTAGGCCC | 5607 |
rs546984141 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659593 | TGAAATTTGAGTACT[G/T]AAATCACTATTTTAG | 5607 |
rs546989894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593298 | CTGTTTCTTTCATTA[G/T]CTTTGGGGAGAAAAG | 5607 |
rs547018169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690682 | GAGATTACAGGTGTC[C/T]GCCACCACGCCCGGC | 5607 |
rs547034846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586975 | GAGTTGGGGTGGGGT[A/G]GGGAAGAAGCTAGAA | 5607 |
rs547040671 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794042 | ACTTGTCTTTCTTAA[C/T]AGTGGAAATAGACTT | 5607 |
rs547096307 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638512 | TGTCTTTGCTATTGC[A/G]AATAGTGCTGCAATG | 5607 |
rs547098527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590554 | GGGTCACCACAGCTT[C/T]GACCTCCTGGCCTCA | 5607 |
rs547110495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632672 | TGCCTTTTTAGCTAT[C/T]CACAGTGAGAAATTG | 5607 |
rs547119207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638972 | TACCCCTTTACTGCA[A/G]AAATTAACTCAAAAT | 5607 |
rs547125685 | snp | A/C | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667219 | ATGCCTTTTTATTTA[A/C]CAAAAAGCTATTTAA | 5607 |
rs547159278 | snp | A/C | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703825 | ATATGTAACTTCCAA[A/C]GGTGATTAGTTTAAA | 5607 |
rs547164529 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679898 | TAAGTTTATAAAGTT[G/T]TGCAACCATAACCAT | 5607 |
rs547164775 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577483 | ACTTGAAGTAATATT[A/G]TGAAGGTTACTTTGT | 5607 |
rs547170719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622864 | AGCACTTTGGGAGGT[A/C]GAGGCAGGTGGATCA | 5607 |
rs547186720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676672 | GTGCTACAGTGTTAG[C/T]TCTCTTGTATGTATA | 5607 |
rs547190009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770843 | GCAGTTTATATTCCA[C/T]AGAAAATATATGTGA | 5607 |
rs547191482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720745 | GTAATTAGTGTATTT[A/T]ATGGGCCTTTGCTTC | 5607 |
rs547246114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663573 | TTCATTAGTTAACTT[C/T]TTAAAAATGTCTCTC | 5607 |
rs547251533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799436 | AGGTGACTTCATTTG[A/G]TCCTTACAACCCACT | 5607 |
rs547263757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763621 | GGAGGTGAGGGTCCA[A/G]TTTTTTTTCATTTTT | 5607 |
rs547285381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608599 | GATCAGGAAAGGCCT[C/G]ATGGAGGAACTGGCA | 5607 |
rs547306962 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797652 | ACTTGGAAATCACTG[G/T]TTTTTTTTAAATTTG | 5607 |
rs547307906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615584 | GAATACTAAAATTTC[A/G]AAGCTTGGCCATTAG | 5607 |
rs547323212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696564 | CTTCTATGCTGTTAG[A/G]TACAGTGGAACCACT | 5607 |
rs547338867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806260 | GGGCACCAACTGAAC[C/T]GGAAAGCTGGCAACA | 5607 |
rs547358981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730843 | TGGAAGGAGCCCTGG[A/G]CCATGAGCCAGAGTA | 5607 |
rs547359468 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739936 | CAGCAACCTTTCTTA[A/C]AATGCCTAGAAACAT | 5607 |
rs547378796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688155 | ACACAGAGCCACAGC[A/G]CAAGAGCATACCTGG | 5607 |
rs547387846 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609869 | CACTCAGGCGGAAGC[C/T]CTAAGATTAAGATAG | 5607 |
rs547407221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612495 | ACCTAGAGGCATAGT[A/G]TCATGTGCAGTGAAG | 5607 |
rs547424649 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636671 | TTTATTGGATACCAG[A/C]CATGTGGCATGGGTG | 5607 |
rs547427584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670315 | CTGGTTGACAAACAG[C/T]GGAGGAGGAGTTGAC | 5607 |
rs547428545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619146 | TCCTCTACCTGGAAT[C/T]CCCTTCCCCTAGATG | 5607 |
rs547437622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760847 | TAATCCACCATGATG[A/G]GACCTACACACCCTG | 5607 |
rs547438392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708838 | AGGTACATTTATGCC[A/T]TAAGCAAAGAAACTT | 5607 |
rs547450944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722859 | AAGGTAATTAAGAAC[A/G]AATTTTAGAACATTT | 5607 |
rs547454108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574650 | GAGGTGGGCGAATCA[C/T]GAAGTAAAGAGATCG | 5607 |
rs547456038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653890 | TATTTTCATTAATCT[C/T]AAAGTATTTTCCATT | 5607 |
rs547464795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584842 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC | 5607 |
rs547467193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671911 | AGTGAAAACATGTGG[G/T]GTTTGGTTTTTTGTC | 5607 |
rs547470163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567589 | CGGGATGGTCTCGAT[C/T]TCCTGACCTCATGAT | 5607 |
rs547473253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723768 | TAAAAAAAAAAACTA[A/G]ACTTAAGCTGCCTAT | 5607 |
rs547481655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67716969 | AGGAAACTTAGATCC[A/C]GATAAGTTAAAGGAC | 5607 |
rs547488549 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679625 | GAGCATATCAGTTCT[A/G]AGAGGAAATAACCAT | 5607 |
rs547523410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716018 | CAAGATGCAGTCATA[C/T]ATTCATTTGGTCACT | 5607 |
rs547527127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707955 | TCCTAGGGTACCTGT[A/G]GTAAAGAAAAAAAAA | 5607 |
rs547535662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745057 | TCTATGCCCAGAAAA[A/G]GGAAGAGGTTCATCT | 5607 |
rs547565131 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715458 | CACTGAATAAAGCAT[C/T]GTTGAGTTTGCTTTG | 5607 |
rs547592301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603953 | AGTGTAATAAAGCTA[A/G]TAAGTGCAAAGCAAA | 5607 |
rs547595190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717753 | GCTTTGGTGGGGATG[A/G]CCAGGAGTGGCTGGG | 5607 |
rs547600392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709366 | GACAAACTAGGAGGG[C/T]AATCCTTCCCTGGAA | 5607 |
rs547601547 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662649 | AGTTTTTAATGGTGA[A/C]CACTGATTAAATTTT | 5607 |
rs547612559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618067 | ATCTTTTAATAAATT[C/T]GCATTAACAGTTTAG | 5607 |
rs547620641 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747218 | ACAGATCAAATGAGT[C/T]TGTATATGGGAAAGA | 5607 |
rs547627367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754026 | ATGTACCTTGAAAAC[A/G]TGCTAAATGAAAGAA | 5607 |
rs547640042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613132 | ATTAAAACTTATCCA[A/G]CCAGCTGCCTATGGC | 5607 |
rs547653152 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804966 | GCCCCAGACCAAACC[A/T]CTGCCATCCACAGGG | 5607 |
rs547666858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711106 | ATGTCATAGTTCCTT[A/G]TGACAGGATTCAAAT | 5607 |
rs547672011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805662 | GCTGGGGGCAGGCAC[A/C]TGGCGCCCTCATCTC | 5607 |
rs547678238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664487 | CAGCCTAGGTGACAG[G/T]GTGACACCCTGTCTC | 5607 |
rs547683075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577081 | GCTGGGACTACAGGC[A/G]CCCGCCACCGTGCCC | 5607 |
rs547683130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568662 | CTGAGTGTAAAAAAT[A/G]ATACTTATTACCAAA | 5607 |
rs547687452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605333 | GCTGGGATTATAGGC[G/T]TGAATCACCACCCCC | 5607 |
rs547715800 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798986 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCATCT | 5607 |
rs547728046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604663 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 5607 |
rs547729998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597040 | TGGGCATGGTGGTGG[A/G]CGCCTGTAGTCCCAG | 5607 |
rs547742081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569189 | TTAAAGAACAAAGAG[A/G]TTAGAAGCTCATTTT | 5607 |
rs547757896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694775 | TATATACCCAAAGGA[C/T]TATAAATCATGCTGC | 5607 |
rs547763586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617222 | TCTGAAATATTTATA[G/T]TAAGATTATAGGCCA | 5607 |
rs547770385 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638275 | TCCCTCTATGTGTCC[A/T]TGTGTTCTCATAAGT | 5607 |
rs547780830 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645964 | GTGTTATAACTTAAC[G/T]GACTTTTAAAGCCAT | 5607 |
rs547783916 | snp | A/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680331 | TTTCTCTTGAGTAAA[A/T]ACCTAGGAGTGGAAT | 5607 |
rs547786256 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566893 | ATGGCATACAGTGGT[G/T]TTTGATACATGTGAC | 5607 |
rs547801377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701741 | GATTCTTATTCTGGA[A/G]GTTCATTTGTATTAA | 5607 |
rs547805217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612518 | CAGTGAAGTCACTCA[A/G]ATTCCTTCTTATTAT | 5607 |
rs547812330 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744957 | ACACATAAGAGTCTG[A/C]CTTACATCAGAATGA | 5607 |
rs547823933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776111 | CTATTGCAGAAATCA[A/G]GAGTCAGCTTTAAAC | 5607 |
rs547835571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804684 | CCCCAAAGTCACCCG[A/G]CATTCTGGGAAAGTG | 5607 |
rs547838743 | in-del | -/A | 0.0418186 | 0.138422 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753670 | AGGATGGCTGTAATT[-/A]AAAAAAAAAAGAAAA | 5607 |
rs547856005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761383 | ATAGCACAGTTTCAC[A/G]TATAATTCTCAGCCT | 5607 |
rs547873983 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734185 | AAGTTTGCTAAATAA[A/T]TGGGTAGTTTTAATT | 5607 |
rs547875039 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564791 | CACACACACAGATGG[A/G]TTCTAATTTTCTCAC | 5607 |
rs547875303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784032 | AAGGATCCTGTTTTA[C/T]AATCTTTAAAAAATT | 5607 |
rs547881149 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776372 | GGACAAATTTTCAGA[C/G]AGTAGAGACCCTGAG | 5607 |
rs547894011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596912 | CATGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 5607 |
rs547895206 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711138 | TGATTCTCTCATAAT[C/G]TTCTATGCTGTTTAG | 5607 |
rs547898995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567222 | GCTGCTCTGCATTTT[G/T]TTATGAGTTTGTGTT | 5607 |
rs547905777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630761 | AAATTACTAATGTTG[C/T]TAGTGTTCTTTGAAA | 5607 |
rs547907051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609775 | CTATCTGAGGAGGTG[C/T]TGTTTGAGCTGAGAC | 5607 |
rs547914605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645236 | TAATCCCAGTGCTTT[C/G]GGAGGCTGAGGTGGG | 5607 |
rs547918381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783299 | TTGCCAGAGACCCCC[A/G]CTCACCTTCTCCTCC | 5607 |
rs547919649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652643 | GTTTTGAAGGGGACA[A/G]ATATTCAAACTGTAT | 5607 |
rs547938390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671709 | GGTACGTGTGCACAA[C/T]GTGCAGGTTAGTTGC | 5607 |
rs547959952 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708209 | GTGCCTATAGTCCTT[C/G]CTATGTGGCAGGCTG | 5607 |
rs547984762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701229 | TTAGGATTTTCATGT[C/T]TGTTAGAAGTTCTTG | 5607 |
rs547995184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670744 | AAAAAAAACCAACCC[C/T]TGTGATTTAAAGGAT | 5607 |
rs547995991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544937 | CCACACAGTCATGCA[C/T]ATACAGATTTCCCCT | 5607 |
rs548007105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753050 | ACTTATATATGCATA[C/G]TCAGTTGTTTTCTGA | 5607 |
rs548050151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805180 | TTCCTCCTCCTCCTC[A/G]CAGCTCTGACAGTGC | 5607 |
rs548065009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790779 | ACACTTAGTGCTGAA[C/T]ATGTGTTAGGTGTTA | 5607 |
rs548069885 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794451 | TTCAGATGGAAAACA[C/T]TGGTCGCTAATAGCA | 5607 |
rs548069973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625366 | TCACAAACAAAATGG[A/G]ACACTCAAGGACCAA | 5607 |
rs548082163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568493 | GAGGCCCACAGAGAA[C/T]AGAAGATTCAGATAT | 5607 |
rs548100716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680283 | ATAATACTACTTTTC[A/G]TACACAAGTCTTTAT | 5607 |
rs548102417 | in-del | -/TTAT | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586421 | ATATTTCATAATTAA[-/TTAT]TTGGACCTCATTTTT | 5607 |
rs548118557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730805 | TTGTCTTCACTAGTG[A/G]CAAATTGAGAGGAGT | 5607 |
rs548152983 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798578 | TTTCTCCCAGTGGTC[A/C]ATTTCTGGCCTATTA | 5607 |
rs548153041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790361 | ATTACACTTCTGAGT[A/G]TGAGGTCTTTCCACA | 5607 |
rs548161161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737106 | AGAGACTGTGAGTCT[A/G]AATGGCCGTCCTTAT | 5607 |
rs548173936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729451 | AGTTAATCAGTGAGA[C/T]TTGATGGGTGATGAG | 5607 |
rs548176163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721315 | ACTGTTTGGGCTCCT[C/T]AAGTAAGTTTATATC | 5607 |
rs548187951 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790123 | TCTTAAAAAAGCAGG[C/G]TTGGAAATTGCAAGG | 5607 |
rs548211159 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737012 | TATTCAGCAACAGGG[C/T]CAGACTGTCTCCCAC | 5607 |
rs548211397 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693957 | TGAACATGCTTTGTC[A/G]CCAGATCAAAATTAA | 5607 |
rs548214242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619046 | CCTCTCTGACCTCAT[C/G]TCCCCCAGCTAGCCC | 5607 |
rs548223990 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589359 | CATGGGTTGTTTTTT[C/T]TTTTGCCTTAGGTGA | 5607 |
rs548227921 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781874 | TAATTGTGGGATTGG[C/T]GTGGCATTGACAAAA | 5607 |
rs548228846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624716 | CTCATTGCACCGTCT[A/G]CCTCCTGGGTTCAAG | 5607 |
rs548244299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678735 | CTTTGGGAAGCCGAG[A/G]CGGTAGGATCATGAG | 5607 |
rs548244479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679980 | TTGGCAATCACTCCC[A/T]GCTCCTGTCCTCAGC | 5607 |
rs548260996 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595303 | TGTCAACAGTTCATA[A/G]GAAACATTTGACTGG | 5607 |
rs548271234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729998 | ACAACTGTATTCCTT[A/G]AATCATGATAGAATG | 5607 |
rs548272025 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766643 | ACAGATTTGAATTAG[A/T]TAACAAAATAGGCAG | 5607 |
rs548272483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723072 | ACTTGATTACTAAAA[A/G]CATGTCTTGAATTTG | 5607 |
rs548303287 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616630 | GCTAATAACAAATAC[A/G]TTTGTAACTTTTATT | 5607 |
rs548327772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800218 | ATCTGAAGTTTTCTC[C/T]GGGGATTAGATTGGT | 5607 |
rs548337059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770139 | CAATACTGGGGTACC[A/G]TTTCAATGAATTTTG | 5607 |
rs548362466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618328 | CTGTTTGTACCTTCT[C/T]GTCTCCTTTACTGTT | 5607 |
rs548401717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723658 | CCAAATCTTTTACGA[C/T]GTGAGCTGCTCCCCT | 5607 |
rs548404845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714628 | CATTTGGTGTGTTTC[A/G]CTCAAATACTGATAT | 5607 |
rs548434999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575368 | ACCCATGGAGGTGGC[A/G]GGGCGGGGGAGGGCA | 5607 |
rs548438931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709770 | ATCTGCAAAAGTGAA[C/T]TTTAAGTGGGTCCTT | 5607 |
rs548449111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762403 | AAGAGAAAAAAGATG[C/T]TCATTGGCTTTGGAA | 5607 |
rs548457768 | in-del | -/AAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687944 | ATGGAGGTAAATGTT[-/AAG]AAGAACACTGAAGCA | 5607 |
rs548465393 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622607 | TCAAACATTTATGAA[A/G]TGAGGAGCACCTACC | 5607 |
rs548470833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611428 | TAACTGACCGAAGGG[A/G]CAAATGAGAAGTTTC | 5607 |
rs548476563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584049 | CCACCATGCCTGGCC[A/G]TAATTCTGATGTAAT | 5607 |
rs548497067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567715 | TTAGAAAAAAAATAC[A/G]CACAACCTACATATT | 5607 |
rs548505338 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642708 | GTTTGTGGTGGGAGT[-/C]AGTGGGAAGAGGAGT | 5607 |
rs548514525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716756 | CTTTCCTCTCTTCCA[A/G]GCTCTTGACATCCTC | 5607 |
rs548553401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623674 | GTGATCTCGGCTCAT[C/T]GTAACCTCCACCTCC | 5607 |
rs548554804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668187 | TGCTAAGAATGTGGC[A/G]TGTTTTTATTATAAC | 5607 |
rs548574684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775405 | CAGGATACGTTTCAG[C/T]TGCTGTGGTTTTCTG | 5607 |
rs548581274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603737 | ACTAAAGTCTCTATA[A/G]AACTAAGTGTTTGAT | 5607 |
rs548601554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566392 | TATTGGCCAGGCTGG[C/T]CTCGAACTCCTGATC | 5607 |
rs548603753 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653181 | TTATTTCTGCAAAGT[C/T]GGTAGTAATGTTCCC | 5607 |
rs548609494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774807 | TATCTCCCAAGCATG[A/G]TAACTCCAGCCAGCA | 5607 |
rs548609629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782542 | CCTCTCTTCTCACAG[A/T]GACCAGGCCTGAGTT | 5607 |
rs548623603 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559734 | ATCATATTACTATGC[-/T]TCCAGGCAACTAGAG | 5607 |
rs548631468 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614548 | TCATCATTAGGCTTT[A/G]TATCTCTTGCTTCTC | 5607 |
rs548640761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613922 | TGTTCTAGAAGAGGT[A/T]ATTTAGTAAATTGTA | 5607 |
rs548645478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797455 | TTTAATTGGATTTAG[A/G]AGCTTAAGTGGATAA | 5607 |
rs548645755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768355 | CATCTTCTTTTTTCC[A/T]CTACATCAAAGCTAT | 5607 |
rs548649484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708705 | CTGCCCATTGCCTTG[C/T]TAATATGCTGTCACA | 5607 |
rs548689284 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660068 | ATTGTTTATATTTGC[C/T]TTTACATTTTTTTTA | 5607 |
rs548696677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573750 | TGTCCTGATGTCCTG[A/G]TATCTTAAGAACAAA | 5607 |
rs548696738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563558 | TCATAAACATTAAGA[A/G]TAATGCATCTTAATG | 5607 |
rs548704127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613393 | CCAAGGAATGTTTGT[G/T]TCATTCGGTCAGAGA | 5607 |
rs548717679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674157 | CGGCCCCAAACACTT[C/T]TTTAAAAGAACTGGT | 5607 |
rs548720438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748482 | ATCTTGCTATATTTT[A/G]TTGCATTAATGATTT | 5607 |
rs548728543 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762235 | AAATCCCTTCGGTAT[A/G]AGACAAGTATGTTTT | 5607 |
rs548754997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711861 | ACGAGATATGTGGAG[A/C]CAGGAGTCAAGGTGG | 5607 |
rs548771533 | snp | A/C/G | 0.000196488 | 0.00991022 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806714 | GTGGGTGTGCCGGGC[A/C/G]CTGGAGGAGAGGCGG | 5607 |
rs548776423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606677 | TGATTTGACTGTAGA[A/G]GCCAACTAAAACATT | 5607 |
rs548784853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804147 | GCCGTCACGACCCCC[C/T]GCCTGCCTGCCTCTG | 5607 |
rs548788301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759227 | TGGGGGATGCTGATG[G/T]CAAGAATGATTGCCT | 5607 |
rs548789721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764989 | ATTTTTAGATTTACA[C/T]ACAGTTGTAAGAAAT | 5607 |
rs548821932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797999 | AAAATGTTTTCTTAC[A/T]CAAGAGGTAAGGAAA | 5607 |
rs548842499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596178 | GTGGCTCATGCCTGT[A/G]ATCCCAGCACTTTAG | 5607 |
rs548846261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552685 | CAAGTGATAGTCCCA[C/T]CTTGGCCTTTCAAAG | 5607 |
rs548864611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693275 | ATAAGTATCCTGCTT[A/G]AGTGAATTGTTTAAG | 5607 |
rs548864914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644280 | GTGCCTGTAATCCCA[A/G]CTACTTGGGAGGCTG | 5607 |
rs548880152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740870 | CCGTCTCTACTAAAA[A/C]TACAAAAATTAGCCA | 5607 |
rs548882330 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749609 | ACACATATCACAATA[A/T]TAGTAAGAGTGGGGC | 5607 |
rs548899408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788355 | TTGTATCACTGCTGG[C/G]TTATACAGGCTGTCC | 5607 |
rs548940936 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725976 | AACAAACATAATCAC[A/G]CAAAACTTCGAAAGG | 5607 |
rs548945526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757202 | TCCACATCCTCACCA[C/T]CCCTAGTTACCTTTT | 5607 |
rs548946517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805479 | GGCCATGCGGCTCTT[G/T]AAGCAGCCTCTCTAG | 5607 |
rs548947823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700429 | CTTTTCACACTGATG[A/G]CAGCTGTCATGTGAG | 5607 |
rs548948257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554597 | CTTCAATGAAACCTC[C/T]GGTGATTCCAGATGG | 5607 |
rs548951969 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738394 | TGGATAGCCCTATGC[C/T]TTCTTGGTAGCCAGG | 5607 |
rs548955411 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540753 | GATGCTTCTCGCAAT[A/G]AGAGTTATAACTTTC | 5607 |
rs548966527 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554843 | TGAAAATTATAAAAT[A/G]TATATGGTCTAAATC | 5607 |
rs549010588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641507 | TTGTGATGAATTGCC[A/G]TATTTATACTGTATA | 5607 |
rs549028116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561677 | AAGAGTGAGAGCTAT[G/T]GGTCACTGAACAGGA | 5607 |
rs549049188 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697179 | CATAATTAGAAGTCA[-/T]TTGATACCCTCATTT | 5607 |
rs549053191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599985 | ATAGAACCTTGAAAA[A/G]CATGCAAACTTATAT | 5607 |
rs549054433 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552392 | TGCTAAGAGCATTCC[A/G]TGGGTTATCTTATTT | 5607 |
rs549085107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553769 | ATACAAAAAATTAGC[C/T]GGGCGCGGTGGCGGG | 5607 |
rs549089355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562659 | AAAGAGCTGCTAAAT[A/G]GAATGGGGGAGACCT | 5607 |
rs549093028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665245 | CCTTGTCTAGTAACA[A/G]AACACATGAGAGAAT | 5607 |
rs549108803 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732959 | ATAGCTCTGTGGGGA[-/G]GGGGGGGCTTAACAG | 5607 |
rs549111948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799349 | GTGCCCTCAAGTGCA[C/G]GACCTGTGCTCTGTG | 5607 |
rs549114882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757826 | CATATAAATTCTATA[A/G]TTAAAGTGTGGCCAA | 5607 |
rs549155134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762956 | CCCAGTGGACAGAAC[A/G]TCACACCAAAATGCC | 5607 |
rs549178736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800955 | GATCACCAGTATTCA[C/G]TGTAACCCTTTGACC | 5607 |
rs549186594 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648748 | TGCCACCATGCCCAG[C/T]TAAGTTTTGTATTTT | 5607 |
rs549186832 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548887 | TAGTCCTCTTTGATC[A/G]GTTTTATATGCACAG | 5607 |
rs549188003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598275 | AAGGTTTGCATAACT[G/T]TAAAACATTGTAGAA | 5607 |
rs549205291 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575750 | AGGTGATGATACTTA[C/T]AGAATAGGATAGGAT | 5607 |
rs549217257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564014 | AGCTATCATGAGGAG[A/G]CATAGGTTACCTGAG | 5607 |
rs549218243 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565706 | TCCTTAGTTTAAAAG[-/T]TTTCTGAGATTACTT | 5607 |
rs549223113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697497 | ATTGCTGTGCCTCTC[A/G]TTATACCCATATTAT | 5607 |
rs549239569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600563 | TGTATTGATCTTCTC[A/G]TTTTTGCAGCTGAAC | 5607 |
rs549256429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555398 | GGGATCCACCCCCAC[A/G]ACAAAAACACCTCCT | 5607 |
rs549257216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586114 | TGTGTATATATTTGC[A/G]TACTGGGGGTTTGGT | 5607 |
rs549259611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702914 | TCCAGACCAATCTAT[C/G]AAAATGCAAATAAGT | 5607 |
rs549285211 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690060 | AGCTATTGTTAGTGT[A/G]TTTTATATGTGGTCC | 5607 |
rs549291244 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573454 | AGATCTCGTGAGAAT[A/C]CACTCACTATCATGA | 5607 |
rs549293453 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679466 | ATGGTTGGTGGACCA[A/G]ATTTTTCATGTTTGA | 5607 |
rs549302369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739602 | TCTCCTGCCTCAGCC[A/G]CCCTAGTAGCTGGGA | 5607 |
rs549313812 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742424 | CTCAGACATTTTGAA[A/G]CATTAAAATGTTGCT | 5607 |
rs549317689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556121 | TATAAACTATTTGTC[A/G]TCTTTGCCTGTTTTT | 5607 |
rs549328089 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570549 | ATAGATTGGCTTCAT[A/G]TGTTATTTTTGACCA | 5607 |
rs549331067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792364 | GAGGTCTTTGAAACA[C/T]TTGGATACACCTCTC | 5607 |
rs549341782 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545994 | CACGAGTGGCCCCAC[C/G]ACTAGAGCTCAGCAT | 5607 |
rs549342518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801743 | ACACAGCAAGTGCTC[A/G]GTAAGTAGATGTATA | 5607 |
rs549360986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724717 | GTGTGGAACATAAAC[A/G]CTGTAGCTGCATTAG | 5607 |
rs549365501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732624 | ATGTTTTCACACCCC[A/G]TTAATTTATTACTTC | 5607 |
rs549384793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654036 | AAGTATCCTTTACAT[A/G]TCAGTTAATTCTGAT | 5607 |
rs549402267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604740 | ACTCTACTAAAAATA[C/T]AAAAATTAGCTGGGC | 5607 |
rs549403503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731542 | GGAGCACAGTCTTAT[C/T]ACTACTGCCTATAAC | 5607 |
rs549417802 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642195 | ATTTTTAGTTTTAAA[-/T]TCAGTTTAAAATCAA | 5607 |
rs549439551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754262 | GTGAATTTTATCTAA[A/G]TTTTAAATGTCAAAG | 5607 |
rs549472944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725395 | TGCTGTATCTCACTC[C/T]GTTTTAAGCCGTCCA | 5607 |
rs549503793 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639099 | GAAGACACCAAAAGC[A/G]ATTGCAACAAAAGCA | 5607 |
rs549504113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626309 | TGGTAGATCACTTGA[C/G]GTCAGAAGTTTGAGA | 5607 |
rs549534573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756237 | AAGGAGACTGCCCCT[A/T]TATGGCAACATTTTC | 5607 |
rs549536964 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584889 | TTTAGGTAGAGACAG[C/G]GTTTCACCATATTGG | 5607 |
rs549539434 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765941 | AGTTTCAGTTGTAAT[A/G]GGTTGACCTTCTTGA | 5607 |
rs549546406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731677 | TATTTCCAGCCTCTA[C/G]GTGAGCCAACTCAGG | 5607 |
rs549551996 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794381 | AACAATCAGAATTTT[C/T]GAAGAGTTTGCTTCC | 5607 |
rs549574544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640349 | ACCATTGCTCTCACC[C/G]AGAATATTTCTTAGC | 5607 |
rs549576340 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554577 | AGTTCTGAGAAATGG[C/T]GTCTCTTCAATGAAA | 5607 |
rs549584587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632892 | CCTAGAATGTGTTAC[A/G]TGGCATTATCAAGTT | 5607 |
rs549647056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757043 | ATAGTGATTTATTTC[C/T]TTTAGATATACACCG | 5607 |
rs549672960 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626396 | GCCAGGTGTGGTGGT[A/G]GGCTCCTGTAATCCC | 5607 |
rs549677304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648171 | CACCACTGTATAATT[C/G]CAAAACACTTTTTAC | 5607 |
rs549682261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655637 | CTTGCTGCTTTCAAG[A/G]TTTTCTTTTTGTCTT | 5607 |
rs549698791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779146 | CAGCTGAGTATTTCC[A/G]TCATGCACAAAAGTC | 5607 |
rs549700400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555276 | AGGCGTGTCACATGG[C/T]GAGAGAGAGTGGAGG | 5607 |
rs549737266 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630111 | TGGTGGCATGTGCCT[A/G]TAGTCCTAGCTACTC | 5607 |
rs549753388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561436 | ATGAAAGAATCTTTA[C/T]GTGTGTAACATCTCT | 5607 |
rs549764522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586512 | TATAACTTGAGGTTC[A/G]CTACTAACCCCTGGG | 5607 |
rs549766112 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799159 | GGGCGACAGAGCGAG[A/T]CTCCGTCTCAAAATA | 5607 |
rs549770407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800842 | CCACAGCAGCCCTCC[C/T]AGCCCATGCTTGCCA | 5607 |
rs549793286 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707324 | TTATTTGTTTTTACC[A/G]TAGTATGTTAGGAAT | 5607 |
rs549820978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701792 | TCTGCGATGGCTGCT[C/G]CAAAAACTGCACATT | 5607 |
rs549846182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605836 | GAGGTTTTAGTGGGG[C/T]TCTTTCATTGGATCT | 5607 |
rs549855097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717841 | TGTTCTAAGCTGTGA[C/T]TGCAAAAGCTACAGA | 5607 |
rs549877303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626975 | TCTCGCTCTGTCACC[C/T]GGGCTGTAGTGGAGT | 5607 |
rs549877465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770954 | AGCTTTTAAAAACTA[C/T]TTTTACTCTGAAAAC | 5607 |
rs549880855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662564 | CACGCTCATGTGCAT[A/G]TAGGATCAGTGGTTA | 5607 |
rs549888522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568334 | TTTGACCTGTGGAGC[A/C]CCTTATAAATTGGGA | 5607 |
rs549891171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716724 | AATCTGGGTCTTCTG[A/T]TGTGAAATGTAGTGC | 5607 |
rs549898443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674009 | ACGTGCCTCCATGCC[C/T]GGCTAATTTTTGTAT | 5607 |
rs549906817 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709636 | AGTGCTTATCTCTTC[A/T]AAAGAATGGCTTAAG | 5607 |
rs549911402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769994 | ACTGAACGGACGTAC[A/G]AAGCTTATTTTTATT | 5607 |
rs549913361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598242 | AAACTAAAAAACTGT[C/G]AATCAGTTCACAGGC | 5607 |
rs549980693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702850 | TTTTTCAAATTTCCT[A/G]TAAGTTTGAAATTAT | 5607 |
rs549985663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806301 | CCTCGGCTGACTGGC[C/T]GTGCGAGTGATGCCG | 5607 |
rs550025543 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606466 | AGGTTGAATGTATAC[C/G]ATTACTTAGGAATTA | 5607 |
rs550038587 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711671 | CACACAGGCGTGCAC[A/G]CACACACACACACAC | 5607 |
rs550058388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656516 | ATATTTTTGGTAGAG[A/G]TGGGGTTTTGCCGTG | 5607 |
rs550063367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570273 | CTTGCTGTCATTTTC[A/T]CTTTCAAGTCATTAA | 5607 |
rs550064964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746344 | TGTGAAACACATTCT[C/G]TTTGATGTCAGAAAT | 5607 |
rs550065339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562874 | ATGCTGTTGTGAGAT[A/G]ATAGATTGCCTGGGA | 5607 |
rs550067355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696202 | TTTGAGTTCTACATG[A/G]GCCCTATGCCAAATA | 5607 |
rs550095164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711826 | TATTGTAAACACCCA[A/G]AGGGTCAGGAATTGG | 5607 |
rs550097210 | snp | A/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704373 | GGGATTGTAGGCAGG[A/G/T]GCCACTGTGCCTGGC | 5607 |
rs550128036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563463 | TGTCATACATTTTTC[G/T]ATATAATAGGTAAAG | 5607 |
rs550130751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799279 | TGCCCAGGTATGCTC[A/G]CTATGTGGACAGGAA | 5607 |
rs550133798 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602339 | TTTTCAAAGCTTGAA[C/T]CTTTCTTCTTAATGC | 5607 |
rs550141855 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553072 | CTGATTATTTTAACT[A/C]TCATTCATTGATAGC | 5607 |
rs550144673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703822 | TGCATATGTAACTTC[C/T]AACGGTGATTAGTTT | 5607 |
rs550145570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705724 | CTGTGTAACAAGAGC[A/G]AAACTCCATCTCAAA | 5607 |
rs550146697 | snp | A/G | 0.000107869 | 0.00734322 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806642 | CTCCTCCTCTTCCCC[A/G]CAGGGCCACCCGTTC | 5607 |
rs550163385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553679 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 5607 |
rs550163787 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542943 | CCCTCTCCTAGTCCA[C/T]TGACGAGCGGTGGAC | 5607 |
rs550185092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661759 | AATTTTTAGTGGTGA[A/G]CTATCTTTAATGGAT | 5607 |
rs550187826 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688272 | CCTCTGGGAGGACTT[C/T]CCATTTTTGCACTGA | 5607 |
rs550196739 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620372 | CGAGACTCTGTCTCA[G/T]AACAGAAACAAAAAC | 5607 |
rs550202002 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618953 | CTCCCCCTCTGCTCA[C/T]GACCTCTTATATCAC | 5607 |
rs550203806 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761535 | GGTGGCAAATGGCAG[G/T]AATTATTTTAACTAA | 5607 |
rs550209384 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798679 | GTACTGTCTAGGATG[G/T]CTAGAGGTAAGCAAT | 5607 |
rs550227300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698409 | TGGCCATGCTGGTCT[C/T]GAACTCCTGGCCTCA | 5607 |
rs550251201 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695271 | TAATGATAATAAATT[A/T]AAAAAAAAAAGATTT | 5607 |
rs550260021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643322 | GTTTTACACAAAAAC[A/G]AAAATGTAAGTGAAT | 5607 |
rs550281603 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754148 | CTGGAGGGGAGAAGG[A/G]AATTGAGAATGACTG | 5607 |
rs550290123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604026 | TGGGAATTTCAAGGG[A/G]TATTATAATCGTGTA | 5607 |
rs550291524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549758 | AGTTTTTGTAAATAC[A/G]TGACGGTTTATTTGT | 5607 |
rs550298599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805091 | GTACCCAGCTGGGCT[C/T]CAGGCCTAGCTCCAC | 5607 |
rs550309239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802542 | AATTGTTGCAATTGG[C/T]CCTCAGAGAATCCAG | 5607 |
rs550313453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587775 | GTCTCAGTAAATTCT[C/T]CCACATCCAGTCCAT | 5607 |
rs550322094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682319 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 5607 |
rs550329170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546457 | TGAAGTCAGCAGTTG[A/G]GGGCTCCAGTCACTG | 5607 |
rs550332559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657629 | TGGTTTCCCAGTTTC[A/T]TGTTCCAATCTGCAA | 5607 |
rs550351408 | in-del | -/ACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563529 | TTATTTTCAAAAGAC[-/ACTT]ACTGATCATATCATA | 5607 |
rs550355641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694823 | ACGTATGTTTATTGT[A/G]GCATTATTCACAATA | 5607 |
rs550360457 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689826 | CCTCTTAATTTCCAG[A/G]CAGCACCTTCTTCCA | 5607 |
rs550361665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584205 | TAGTAATTCCTGACC[C/T]GATAACTTTAGGAAA | 5607 |
rs550374780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594263 | TAGATTGAGGTCCAC[A/G]TCTGTATCACCTCAG | 5607 |
rs550444469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646145 | AAGAATAAAGGAACT[A/G]CCATGTTTTTAGTTC | 5607 |
rs550445320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600818 | TCCAAGTTCTCTGTG[A/G]CAAAGATTTTTAAAT | 5607 |
rs550450185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588394 | TGTCCCTGATTACTA[A/C]CCATCCCCAGTGCAC | 5607 |
rs550453695 | in-del | -/ACACACAA | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711687 | CACACACACACACAC[-/ACACACAA]AAGGATAATACCATA | 5607 |
rs550455226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595232 | TGTGATATAAATATT[G/T]ATTTCTTTTCTGTCA | 5607 |
rs550481763 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543278 | CTCTTGGAGCCCCCT[C/T]CTAACCAGCGGCCAG | 5607 |
rs550492482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784766 | CTGTCTGGTCACAAA[A/C]CTTTCTGCCTTTCCA | 5607 |
rs550501905 | snp | C/T | 6.61835e-05 | 0.00575216 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692439 | CAAACGCTGTAGATA[C/T]ATGGAATTAGTTACA | 5607 |
rs550512375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580885 | GTTTCATCAACAGTT[A/G]TGTTTCCAAAGGTTT | 5607 |
rs550516428 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595874 | CCCTTGATTTGAAAC[G/T]CATTAGAAATAGCCC | 5607 |
rs550517173 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639677 | TAAAGACTTTAGAGG[A/T]TGGAATTCAAGATCC | 5607 |
rs550520480 | snp | A/G | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807273 | CGCAGTTGTGCTGAG[A/G]CCCACAGCCCAGCTC | 5607 |
rs550526839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787248 | GTTTCTCAAATTTTG[C/T]GAAGGTCTCTAGCCA | 5607 |
rs550529554 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791439 | TCAGGCATCATTACC[A/G]TCTTAGAGTGCAGTG | 5607 |
rs550542633 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540678 | ATTCAATTTGGTAAA[A/G]ATCAGAAAGTTATAT | 5607 |
rs550546812 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641369 | AAAGACAATTATGTC[A/G]CCATAGATTAAATAA | 5607 |
rs550547361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742333 | GGCAAAGAATTGTAC[A/T]AGGTGACTTCCAACA | 5607 |
rs550564085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758934 | GACAACTTAGCATTG[C/T]AGACATGCTCAAAGG | 5607 |
rs550573207 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604116 | TCACAGTTGTACAAT[A/G]TGAAATTCTGGCCCC | 5607 |
rs550584177 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598367 | TGCTCTTCAAAACCA[-/T]TTTTATCTTTATGAG | 5607 |
rs550595030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615412 | ATAGTTTACATAAAA[A/G]CTTCTTTTTACAACT | 5607 |
rs550605897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748381 | AAATGCAAACCTTTA[A/T]CTGCCTGTATTAGAT | 5607 |
rs550610154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640714 | CAAAATGTTTCTCAT[A/G]TTATGCTTCTAAATG | 5607 |
rs550638447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758350 | TGGGCAGTCAGGTGC[A/G]TGGTGGTACTCTCCT | 5607 |
rs550639794 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569513 | AAAAAAGAAAACTTT[C/T]TTCCAGAGACAGATT | 5607 |
rs550657578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740852 | GGCCAACATGGCGAA[A/G]CCCCGTCTCTACTAA | 5607 |
rs550659295 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629629 | ACAACTGGGCAGGTG[A/C]AGATGAGGAATTCCT | 5607 |
rs550661136 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601541 | TTTCCATGTATACAC[A/T]AATCCTGCATCACAT | 5607 |
rs550662182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650798 | AGTTTTCTTTTTTTG[A/T]GATGTCAGTGTCTGA | 5607 |
rs550672797 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756202 | AATGAACTCTAGGAT[-/AAA]CCACCTGTTCCTGAT | 5607 |
rs550694702 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786268 | ACACTGAATTGGTAG[C/T]CTCTTGGGGTGGTCT | 5607 |
rs550696677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706238 | GAGACTCTTTGTAGT[A/G]TAAGGAAGGAGATTG | 5607 |
rs550731812 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588985 | ATCCCTGATTAAGTG[-/T]TTTTTTTTTTATTTT | 5607 |
rs550750710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627929 | AACTTTGAAACAACC[A/G]ATGAGAGCCTGAGGA | 5607 |
rs550769626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780461 | TTGGTTGCACATGCT[A/G]TTCTCTCTAATCCAA | 5607 |
rs550776303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796070 | TTGATTATCCTTTAC[C/T]TCTGTGCTCTTTTAC | 5607 |
rs550779531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675161 | CAAGTGTTTATTGCA[A/G]CTCTATTCATCATAG | 5607 |
rs550804958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550155 | GTTTATGGGTGGCAT[G/T]ACTTTAGAAACTGAC | 5607 |
rs550810103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634532 | TATCAATTACTGAAA[A/G]AGGGGTGTTGAAATA | 5607 |
rs550834829 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807477 | AGCCCCACCCCTGCT[C/T]CTCACTGCCCTTGAC | 5607 |
rs550837658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751465 | TCCCTAAGTCCCTGA[A/G]TACCTGCGTTGTAAA | 5607 |
rs550843715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642625 | AGCAGGAGCAAAGGC[A/T]GTAAGTAGGGAAAGC | 5607 |
rs550868697 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542508 | CTGAGCGAGCAAGAC[A/C]AGTCTCTCCCCGACT | 5607 |
rs550888846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782161 | GTAGTAGATAAGAAA[A/C]TGTTCCTTTCACAAA | 5607 |
rs550906896 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650234 | TGTGGATTCCTTAGG[G/T]TTCTCTATATACAAG | 5607 |
rs550920337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629246 | GGTGGTGGCAGGGCC[C/T]AGCTGCTACAAAGAA | 5607 |
rs550941498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712052 | CAAAACTGAGTGGAG[C/T]GTTTTCTGGAGCAAA | 5607 |
rs550943975 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722168 | ACTTCATCAGTCTCT[A/G]TTACTCGCACTTATG | 5607 |
rs550964967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599760 | ACACCTTTATTAAAT[C/T]CACTTAGTGAATAAA | 5607 |
rs550967121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579004 | GTAACTGAAATTACT[A/G]GCCTATTGTACATAG | 5607 |
rs550973445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765937 | AAACAGTTTCAGTTG[C/T]AATGGGTTGACCTTC | 5607 |
rs550994011 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692279 | TAGAAACCAGAAATC[A/G]TTGAACGTGGAGGAG | 5607 |
rs550999127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696610 | GACTTGGGTGAAACA[C/G]GGAACACGACATTAT | 5607 |
rs551005430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556012 | ACTGGTCTCAAACTC[C/G]TGACCTCAGGTGATC | 5607 |
rs551011004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591902 | AGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 5607 |
rs551016944 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705605 | GCTGGGTGTGGTGGT[A/G/T]TACACCTGTAATCCC | 5607 |
rs551028436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571461 | CAATAAACCAGTTAA[A/G]TTCTACCACTGTACT | 5607 |
rs551028993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571225 | TTTTCCCCCAGAAAA[G/T]TCACATAATGCAGCA | 5607 |
rs551034321 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690596 | TACAGTGCAGTGGCA[C/G]CATCTCAGCTCACTG | 5607 |
rs551070930 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548803 | TCAAAAAGTTGATGT[G/T]TCATTTGTGAGGACT | 5607 |
rs551083005 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586873 | GCCGGACCCTCTCAA[C/T]ACAGCAGCCCAGCAG | 5607 |
rs551083665 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556247 | TTATTGCTCTTTTCG[G/T]TTTGTTCTGGTCTTC | 5607 |
rs551086028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614064 | AACTGAAATTAGAGG[A/C]TCTAGAAGCAACCAG | 5607 |
rs551089543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793988 | GACCCTTGGTAAAAT[A/G]GACACAGCTACCATT | 5607 |
rs551090295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572081 | AAGAAGTGTCTAATC[C/T]AGCTTTGGGGACCAA | 5607 |
rs551116569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671489 | CCTTAGCTAAGAAAA[C/T]GTTGCTTTCTAAACC | 5607 |
rs551121954 | in-del | -/TGTATTCCAGAGAGTGTT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579453 | ACATTTGCCTTAGTA[-/TGTATTCCAGAGAGTGTT]TCACATGTTTATGCC | 5607 |
rs551153133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801820 | AGGCATTGCACCAGG[C/T]CCTGCAGCCACACCA | 5607 |
rs551171544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683560 | TGAGGTCAGGAGTTC[A/G]AGACCAGCTTGGCCA | 5607 |
rs551181776 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659000 | AGTCTATGAGAAAAT[A/G]TTAATTTATTAAGAA | 5607 |
rs551195696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726998 | GAGGTCAGGAGCTCA[A/C]GACCAGCCTGGCCAA | 5607 |
rs551222165 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682759 | AATGGTGTGAACCCA[G/T]GAGGCAGAGCTTGCA | 5607 |
rs551222667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606725 | CTGGAATCATATTAG[C/T]TCATTATAGTAATAT | 5607 |
rs551232418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726161 | TACAAGATATGAGTA[C/T]AAGGTAATGAAACTA | 5607 |
rs551237915 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765232 | GGTGTGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT | 5607 |
rs551239502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773642 | ATAAAATAACAGTAC[A/G]TTTCCTTTTTGCATC | 5607 |
rs551242254 | snp | A/C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733343 | AAGATATTCTTGTAA[A/C/T]GATCCAGTTTATCTG | 5607 |
rs551253706 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697842 | GAAAGCGTAAAATAT[A/G]GAAAAGATAATTAGG | 5607 |
rs551290050 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551610 | AGTGTTGGGATTATA[A/G]ATGTCAGCCACTGTG | 5607 |
rs551292926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579812 | AGCAAACAATAGTAA[A/T]CAAGGAGGGATTTCC | 5607 |
rs551293668 | snp | C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548033 | TGTTCTTTCTCCCTT[C/T]TCCTCGTATCAGGTG | 5607 |
rs551294324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697571 | AGATTTATTCTGCTC[A/G]CTCTATATATCCAGT | 5607 |
rs551296004 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725986 | ATCACACAAAACTTC[A/G]AAAGGGAGTTTGGCA | 5607 |
rs551304240 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569084 | GTCCTTACCTACAAG[A/G]CTGTGTTTTACCTTG | 5607 |
rs551311855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601372 | ACAGGGAGGTCTTCT[C/T]ATGCAGTAGTGCAAA | 5607 |
rs551319016 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738265 | GAAACAAGTTGCAGA[A/G]AGCACTCTTCTGGGC | 5607 |
rs551321380 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668792 | AATCATTCTGGGGCC[A/G]TCTTACACAGATGCA | 5607 |
rs551335677 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719919 | GTGCACAGAATACCA[C/T]GGAAAAAGACCTTTG | 5607 |
rs551340196 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547659 | ACAGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 5607 |
rs551350042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564901 | TTGGGTATGATCTTA[A/C]AAATTGTGCTTTTTG | 5607 |
rs551360112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772905 | GTTTTTGAAGCTCAT[A/G]TCCTCAGATAATAGT | 5607 |
rs551365489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656668 | AACTTCAAAGGTTCA[A/G]GTCCTCTCTGAGCTC | 5607 |
rs551372211 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587377 | TTGGTGCACTGGCTA[A/G]CAGTTAGAGGGCTTT | 5607 |
rs551388490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646733 | CTAATTGGTGGTTTG[A/G]TATTTGATTCTTTTG | 5607 |
rs551392112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622040 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCACA | 5607 |
rs551418000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793109 | CTCTATCCTCTTAAA[C/T]AGATTACATGCATCA | 5607 |
rs551418479 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633937 | GAGATTTTCCATCTT[C/T]CTATTACTGATTTCT | 5607 |
rs551431214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690814 | GTTGGGATTACATGC[A/G]TGAGCCACTGCTCCC | 5607 |
rs551444527 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689310 | ATCATATGCTTTGTC[C/G]CAAACAAATGGTACA | 5607 |
rs551446214 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668146 | TTGGTTGAGATATAT[A/G]TGCAGGGACTTTATA | 5607 |
rs551458340 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701366 | ACTGCATACCTGTTA[C/T]GTGTCAGGTAAGGTA | 5607 |
rs551480552 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729403 | AAAGGTTGAGAATGT[A/G]GCAATATTCTTGAGA | 5607 |
rs551487476 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758003 | GGGGTGTTTGGGCAA[C/G]TATTATGAGATATAA | 5607 |
rs551500660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703757 | TACTAAATCTGGAGA[A/G]CCCGTGATGTAAAAT | 5607 |
rs551507995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657465 | ATGAGAACATAAAAC[A/G]TTTTTCTGCTGTATT | 5607 |
rs551515711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750555 | TGCATCAGAATTACC[C/T]AAGGCTCTTGTTGTA | 5607 |
rs551537376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554727 | TTAGTGATAGGTACG[A/C]TGTTTTATTCCACTC | 5607 |
rs551561852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578814 | TCAATTTCATGCATG[C/T]GAGGTTTTATAGTAG | 5607 |
rs551569402 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558206 | CTTATTTTTGAATCC[C/T]TACCATAATGGTACC | 5607 |
rs551569414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591829 | TCAATAAGGACTTTC[A/T]CGCCAGGGGTGGTGG | 5607 |
rs551571880 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786114 | GAGGTCATTCAGCCT[C/G]TTTGGGTCATGATTT | 5607 |
rs551578198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682010 | ACAGAAGAAAGGCTG[G/T]GATGTTTTTAAGTGA | 5607 |
rs551579124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794243 | AACATTACCTTGGAA[A/G]CCACAGTAAATCAAT | 5607 |
rs551603785 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640578 | ACCTGCAGGGTCTGA[A/C/T]GCCTGCATGGAATGA | 5607 |
rs551606679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557170 | TGATAAAAATCAACC[A/G]TGCCCACTAATGCAT | 5607 |
rs551608381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635935 | ATCTTTAATGTCTCT[A/G]CTTAACATGTTTAAA | 5607 |
rs551629544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696112 | CTGACAGTCTCTTGA[A/G]AGAAAAGAGCTGAGC | 5607 |
rs551638036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691767 | TGTGTCATTACTTAG[C/T]GACTGACTGCTTTGG | 5607 |
rs551650988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758849 | CTATCACTGATTTGA[A/G]GAAAGTACAAAGTGA | 5607 |
rs551653050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787204 | GGCTGAAGCTGATTC[A/G]TGCATAGGAATGTCC | 5607 |
rs551676191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742187 | TGAGCCACTGCGCCC[A/G]GCCAAGAAAGAACTT | 5607 |
rs551697933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578096 | CCTCTGGGTAGAGCC[C/T]GTCTTGATTTTACAA | 5607 |
rs551700349 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698349 | TGCACCACCACGCCC[A/G]GCTAATTTTTGTATT | 5607 |
rs551705124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586194 | ATAATCCTAGGTGCT[A/G]GTATCTACAAAGATT | 5607 |
rs551739587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644186 | ATCACCTGAGGTCAG[A/G]AATTCGAGACCAGCC | 5607 |
rs551765647 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707714 | TTTCACACAAAGGAA[C/T]TGACATTTAAGGGAG | 5607 |
rs551777147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772228 | TTATATACTTCTTGT[C/T]ATTCGGAGTAACAGT | 5607 |
rs551785101 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725701 | GTTTTCTAACTCCAA[A/G]TGGAAGTATATGCAA | 5607 |
rs551787322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674980 | GCAGAAAATTGGATC[A/G]CTAATACATTGCTGG | 5607 |
rs551801499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746550 | AGGTAGTTTGGCTTG[C/T]TACTGAAATTCTTAA | 5607 |
rs551802607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643648 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 5607 |
rs551810625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598538 | CTGCACTCCTTCCCC[A/G]CCTGTGCCCTGACAG | 5607 |
rs551810639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605704 | CCCCAGGCAGTGTTG[C/T]CTCAAGGTCAAGCAG | 5607 |
rs551810718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782645 | TAAATTTTGTTTCAA[C/T]CAACCCCTGTGCTCA | 5607 |
rs551827483 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678819 | AAATACAAAAATTAG[C/T]GGGGCATGGTGGTGA | 5607 |
rs551837874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696589 | ACCACTCTATAATGT[A/T]GATAAGACTTGGGTG | 5607 |
rs551853811 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618222 | TTTTCTGAACACTTT[G/T]TGCAAAGTACTTCGC | 5607 |
rs551867021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748328 | CCTTTGCATGCTTGA[A/G]TGCCTTGTTTTAAAC | 5607 |
rs551869210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555178 | AGAGCTCACAGTTCT[A/G]CAGGCTGTACAAGCA | 5607 |
rs551869510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543581 | TGGCTACTGCTGGCT[C/T]CCTGTGGAGGCAGTT | 5607 |
rs551886513 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743243 | TGAGTAGATCTTAGA[A/G]TGCGAGAATCGTTGG | 5607 |
rs551912506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679852 | AATTTGCATGCCATA[A/T]AATTCATCTACTCAA | 5607 |
rs551924530 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555068 | GATGAGGAGAGGGAC[A/G]TCTGTCTGCAGAACT | 5607 |
rs551945915 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740491 | CAGCTACTCAGGAGG[C/T]GGAGGTGGGAGGATC | 5607 |
rs551953925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598935 | AAATCAGGTTGTTAC[A/G]GACATGTTTAGATTA | 5607 |
rs551963216 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583068 | TACGCATCATCATCT[A/G]TAATCCTCCTGATAG | 5607 |
rs551965408 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796637 | GATTTGAGTGAGGTC[A/G]AATATCCAAACTATT | 5607 |
rs551968793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693703 | GTCAATCTAGTCATG[A/G]TCTGATTTTTAAATC | 5607 |
rs551969321 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779273 | GCTTATAAAGAGGAA[A/C]CCACTAGTAAAGAAG | 5607 |
rs551971620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592452 | TGAATACCAGGATTT[A/G]TTTGTACTACATATT | 5607 |
rs551973957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679127 | AAGGGTAACCTCCCA[C/T]CCTGACCCCTGATTG | 5607 |
rs551994096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641226 | ATATTGCATGTGCCA[A/G]TTATCATTCTTTGAC | 5607 |
rs552007907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744721 | ATTGCTTTTTATCAC[C/T]AGAGCCATTGGCTAA | 5607 |
rs552026094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797935 | TGATCCACCCGCTTC[A/G]GCCTCCCAAAGTGCT | 5607 |
rs552026777 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607534 | TATTATTGGCATCCA[A/G]CCAACATGACAGGAT | 5607 |
rs552031495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740708 | CTTCTCTCATTTGAG[C/G]CAACTGTGTGATAAG | 5607 |
rs552038030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732902 | ATGCACCTGAGATTC[A/G]GATGATTAGTGTGTT | 5607 |
rs552038919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780386 | AAGTTCCTTGAAGGA[A/G]GATCATGATCTTATA | 5607 |
rs552047813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670656 | ATCTTCATGGTTCCT[A/G]ACAAATCCTACCTAG | 5607 |
rs552087477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575289 | GGAAATCCTGCATTT[A/G]AAGGAGAGATGGGGT | 5607 |
rs552090206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574735 | AGCTGGGCGTGGTGT[C/T]GGGCGCCTGTAGTCC | 5607 |
rs552105850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686486 | GTGGCAGGCGCCTGT[A/G]ATCCTGGCTACTCAG | 5607 |
rs552108046 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642511 | AGGTGAGCTTCATGG[A/G]GACAATGGTGGCATT | 5607 |
rs552111098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743959 | TACTCCAAAGTTCAT[A/G]CGTTTTCCTCACAGT | 5607 |
rs552111296 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635248 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCCGCC | 5607 |
rs552123448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627837 | TCATTAAAGTCTCTG[C/T]TCTCCCTGCTGTCAT | 5607 |
rs552127406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797213 | GTCCCCTTGTTTTTA[G/T]ATCTTAAAAATCATT | 5607 |
rs552138001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607937 | GGTAAAAATCAATAC[A/G]TTATGGTAATATTTC | 5607 |
rs552149266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727790 | AATAATTTAGTTTGT[A/G]CATTCAAGGTTGTGA | 5607 |
rs552151273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735644 | AGAGGAAAAGGGAGT[G/T]GTCAGCTCACTTCAG | 5607 |
rs552157852 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561259 | TACATCATTTGTACT[G/T]TGTTTTTTCCTGTCT | 5607 |
rs552158751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723552 | TGCTAAATCTTAAGT[A/G]TTTGGAATTAAAGTG | 5607 |
rs552179297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679595 | AATATTTGTAATTGC[A/G]GTTTATCAGGCCTAG | 5607 |
rs552196867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752279 | ACCATGTTGGCCAGG[C/T]TGTTCTCGAACTCCT | 5607 |
rs552203046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629937 | AGTATATGTGTAAAG[G/T]CCACATTTCATTTAA | 5607 |
rs552205200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550873 | GCCTCCTGGGTTCAA[A/G]CAGTTCTCATGCCTC | 5607 |
rs552213565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595487 | TACATATAAAATAAG[A/G]ATTAATTGAGCATTT | 5607 |
rs552217489 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804718 | CTGTGTTACCCCGGG[C/T]GTGGGGGGAGGGGCC | 5607 |
rs552231579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686075 | AGCTAACCCAAAAGA[A/G]AGCAGGAAAAGAAGA | 5607 |
rs552251858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550792 | CTTTTTTTTTTTTGC[C/T]GCAGACTCTCACTGT | 5607 |
rs552252854 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795257 | TCCTTCATGTTCTTT[A/G]TTATTTGCCATCTTA | 5607 |
rs552285002 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802333 | ATGATATTTTCACCA[A/G]TGTCCCTCATTGTGC | 5607 |
rs552291881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581417 | TGGCAGTACTATCCT[C/T]GTATCAGATATGATT | 5607 |
rs552293343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693233 | AAATTGACTTTTTAT[A/G]TCAGGCGGGTTTGGG | 5607 |
rs552308359 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622935 | AAGCCCATCTCTACT[-/A]AAAATACAAAAACAA | 5607 |
rs552316973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768317 | CATTGATAATGACAC[A/G]CATATTGCAGAGGTG | 5607 |
rs552350064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596133 | CTTCAAAAAGCCTCT[A/G]GAAAAACTTTTTGTA | 5607 |
rs552355298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615639 | CCTTCAAATAAACCT[A/G]AAAAGACCAAGAAAT | 5607 |
rs552383595 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650660 | GCAAAATGAACCAGT[C/G]TTGCAGTGTTGGAAT | 5607 |
rs552419493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716209 | AGCTGCACATGGTGA[C/T]GCACACCAGTAGTCC | 5607 |
rs552420682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629115 | AGCAGCAGTAGCTAC[A/G]GCAGTGGCAGAAGAT | 5607 |
rs552431247 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760566 | CATAATTTTGATTTA[C/G]TAAGTCAATTAGATT | 5607 |
rs552438037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769487 | TTTAATTGGGTGAGG[C/G]CTTATTCTCATTGTA | 5607 |
rs552438419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729573 | CAGGAGATTGAGACC[A/G]TCCTGGCTAACATGG | 5607 |
rs552452756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722934 | AAATGCTTATTTTCA[A/G]TTTGTAGTTATGCCG | 5607 |
rs552467813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618173 | TAATCAGTTGGATTT[A/G]TCCCTAAGTATTGCT | 5607 |
rs552473263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776220 | CCCACCCCCACCTCC[A/T]CTTCTGCCTCCAATT | 5607 |
rs552504317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710767 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 5607 |
rs552530875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624578 | TAAAAAAATTAAACA[G/T]CACGATCTCTTTGTG | 5607 |
rs552563018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684869 | ATTGTGATATTGAGG[C/T]TAAAGATCTGGAAAT | 5607 |
rs552563039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676791 | AAAACTTGCTTAGTT[A/G]TAGGAAAAGTCATAG | 5607 |
rs552563758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587698 | CAGAACGTGGTTGTT[C/T]CCTCTTCCAGGTCAA | 5607 |
rs552566467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609676 | TATTCTATAGGTCTG[C/T]AGATTCTGTAGACCT | 5607 |
rs552566595 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580340 | ATTTTATACACAAAT[C/T]GAATAATGTTTGATT | 5607 |
rs552569943 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654460 | ACAGCATATAGTTGG[A/G]TCATTTTTTTAAAAA | 5607 |
rs552580444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751659 | CTAACATCTATTTGT[A/T]CTTGGCAGCCTGTTG | 5607 |
rs552609555 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786710 | CCTCTCCTAGCTGTC[C/T]ATCCTGCAACATGTT | 5607 |
rs552610180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549838 | AAAGTTTCCTTAAAT[A/G]TTTTTCTTCCTGGAA | 5607 |
rs552617189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788140 | GTGTTGCCTTTGATG[C/T]TGATTTATATGTAAT | 5607 |
rs552623422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684289 | AATTCCAATAATCCA[A/G]TGTAGAGAGGCCTCA | 5607 |
rs552633937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774660 | GCTTTAATTTTTCCT[C/T]TTCTCTTCCCACCTA | 5607 |
rs552638536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684473 | ATATATTACTTGCCA[A/G]TATCAAGTCCAACAC | 5607 |
rs552679065 | snp | A/G | 3.29701e-05 | 0.00406005 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580796 | GTAAATGGACAGTTA[A/G]TAGAGCCTCTGCAGA | 5607 |
rs552698961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677822 | GGCCTTTTTGCCCTT[A/G]TTATTAATCTTGTAA | 5607 |
rs552700042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683813 | TACTTCTGCCCATGG[A/T]GTCACTGCTGTGGGA | 5607 |
rs552712006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659928 | GAGTAGGAAGACTGT[C/T]GAAGTGAATAGAGTC | 5607 |
rs552725393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554833 | CATATTCAAATGAAA[A/G]TTATAAAATGTATAT | 5607 |
rs552736286 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717331 | AACCTAATCTCCAGT[A/C]TGTCTACTGTAATAG | 5607 |
rs552742523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720942 | ACCTCAATGTATCAC[A/G]CTTTTCAGCATTCAT | 5607 |
rs552753943 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541098 | TATTTTTCACAGAAG[C/T]GAAGTGCAGGTGAAA | 5607 |
rs552776317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587870 | CCTGTCAGTCCCCAC[A/G]CTTGTGGGTTCTACC | 5607 |
rs552789419 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723371 | TTATAGATTGTGGTT[G/T]GCCAAGTCAAAGGTC | 5607 |
rs552800161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804134 | CAGGGTCTCCAGTGC[C/T]GTCACGACCCCCCGC | 5607 |
rs552805814 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804875 | TTTGGGAAAGCAGCC[A/G]TGGGGTGGGCATATA | 5607 |
rs552809162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727453 | GGATGAAAATAATGG[C/T]GCAGTTTTCAATTTC | 5607 |
rs552816196 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714700 | GTGAAATCTTACTAC[A/G]TGTTGAATATTCCTA | 5607 |
rs552826560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572642 | TGCTCTGCTACAAGG[C/G]TTTGTGATAAAGGAT | 5607 |
rs552831495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780720 | AAATTTGGTGCCAAA[A/G]TAATAAAATTTCTAG | 5607 |
rs552835087 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768106 | TTGGCTGCCTTGACC[C/G]CCTTAGTTCCTTTTG | 5607 |
rs552868728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573616 | GGTAAAATGAGGCTG[C/T]GACCTGCTGGGCCGC | 5607 |
rs552872823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699435 | CTCTTCCCCCAGTCC[C/T]GGGAAACTGAAGAGG | 5607 |
rs552873517 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609242 | TCATTTTTCACTGAA[A/C]ATCCTGTCACTGTGC | 5607 |
rs552908423 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695788 | TTATGGATGAATGTG[A/G]TGCATCCATCTGTTA | 5607 |
rs552908619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664986 | CTTCCTTCTATTAAC[A/G]TTTCAGATAGCATCA | 5607 |
rs552930189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566332 | GGTGCCCGCCACCAC[A/G]CACGGCTAATTTTTG | 5607 |
rs552932934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627949 | GAGCCTGAGGAGCCA[C/T]TTTAAGCAATGGGGA | 5607 |
rs552937883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622498 | AACTTCTACTCATAA[G/T]ATTATGAAGTTAATG | 5607 |
rs552958414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706603 | AAGAGGAATCAGATT[A/G]TGATCATCAGAGAGG | 5607 |
rs552979732 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795866 | CCTTGCATTCCTGTC[C/T]ATTTTTGCTTTATAT | 5607 |
rs552980805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759286 | GGGTTAGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 5607 |
rs552997043 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721400 | GGCACCCGTTAAGGC[A/G/T]CACTCCTGATGGGAC | 5607 |
rs553025485 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752174 | GGGTTCAAGCGATTC[A/T]CCTGTCCCAGCCTCC | 5607 |
rs553044402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742055 | GTCTGCCACCACACC[C/T]GGCTAATTTTTTGTA | 5607 |
rs553047134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735141 | CCAGTGTCAAATTCT[C/T]CTCCATATCTATTGT | 5607 |
rs553047413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665721 | ATGGAATCATAAACT[A/G]GATTTATTTTTAAAG | 5607 |
rs553050105 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734146 | CTTTCATTTAAAACC[A/G]ATTAATTTATTTGCT | 5607 |
rs553055183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541783 | AATCGCTTGAATCCG[A/G]GAGGCTGAGGTTGTG | 5607 |
rs553076405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772402 | GCTTTTTTCACATTC[A/G]CTTCAAAAGTAGAAT | 5607 |
rs553090092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667714 | AGATTAAGAAATGGA[C/G]ATGTGTTCAGTATCT | 5607 |
rs553097203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563823 | CCATAATACTCCCAC[C/T]GAAAATGAACTACAG | 5607 |
rs553104966 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657687 | ATCATTTTTCTCTAT[C/G]TGCTTTAAATGGGAT | 5607 |
rs553111832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636253 | TTCTACTAAAAATAC[A/T]AAAAATTAGCTGGCC | 5607 |
rs553114425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623117 | AAAAAAAAAGAAAGC[A/G]TATTAAAGGGAGGTA | 5607 |
rs553134072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708851 | CCTTAAGCAAAGAAA[C/T]TTTAATATCAGACTA | 5607 |
rs553136830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566008 | TTGATTGGTAGTCCT[A/C]ATGATTACCAGCATG | 5607 |
rs553140932 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541012 | AAAATCTCTAGTTTC[A/G]TGGTCTATTTTCTAA | 5607 |
rs553143593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801314 | TCACCTGATCACAGG[A/G]CTGCCCTGTCCCAAC | 5607 |
rs553147950 | snp | C/T | 0.000371471 | 0.0136234 | missense, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549196 | ATGATGGAGGGTCAC[C/T]TTCCCCAGAGCGTAG | 5607 |
rs553160874 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721262 | GAATGCAGAACCTTC[C/T]GAATGGTAGATAAGT | 5607 |
rs553161746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728079 | AAGTGGTATCTTAAA[A/G]GGTTCATTTAGAAAT | 5607 |
rs553168014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657027 | GAAAAGGACAAAATG[A/C]ATCAGTGATGGCACA | 5607 |
rs553168204 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602563 | TAGAAGGGAAGAAGC[A/G]TAAGACCATGAAACC | 5607 |
rs553180729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765344 | AGCCTGGTGACAGAG[C/T]GAGACTCCATCTAAT | 5607 |
rs553219482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794488 | TGAGAATAATTGGTA[A/C]TTTTCAATCCTGTAG | 5607 |
rs553219831 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543949 | AGGGCCTCACTCTGT[C/T]GCTCAGGCTGCAGTG | 5607 |
rs553224203 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717377 | GGATCTCATCTAATT[A/C]GTAAATATTTATCAA | 5607 |
rs553228916 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567388 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 5607 |
rs553243484 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658010 | TACTCTGGAATACAA[-/T]TTTTTTATAGAACTG | 5607 |
rs553248794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628920 | AATGGATTTAGTAAT[A/G]ATGGAAGCAATTTTG | 5607 |
rs553267983 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783488 | AACTGGCACAACCTC[-/TG]TGAAGCTTTGCTAAG | 5607 |
rs553268860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705301 | TAGGCAATGGGGATA[A/G]AGTAAGGAAAAGACA | 5607 |
rs553286580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556492 | TATTGTGGGTTTTTA[C/T]AAAAAGCATGTATTT | 5607 |
rs553291240 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757768 | ATTTTAACCACTCAC[A/G]TAAATGGGTATTTAC | 5607 |
rs553291836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767875 | GCAAGATTTTATTTC[A/G]CTCCCATTTTTCCTT | 5607 |
rs553291963 | in-del | -/CCGGA | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576975 | GCTCTGTCGCCCAGG[-/CCGGA]CTGCGGACTGCAGTG | 5607 |
rs553292248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675404 | GACAAAATTATAGAA[A/G]TGGAGAGAGCACATT | 5607 |
rs553319944 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806997 | GTAAAGGGTGGGGCA[C/T]TGAGAATGGAGGCTC | 5607 |
rs553320195 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771356 | TGCTAATCTTATCTC[A/G]CTGTGTGGTCTGAGA | 5607 |
rs553325106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726431 | TACAAATAATTTACA[C/T]GATGAACAAGCTGAG | 5607 |
rs553328840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766923 | AAATTCTCCCTTGAG[C/T]GATGCAGGAGACATG | 5607 |
rs553337235 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571522 | TGGTTTCTGTGTCAC[C/G]CTATTGTTGCGAACA | 5607 |
rs553351735 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729729 | AGATCACGCCACTGC[A/C]CTCCAGCCTGGGCAA | 5607 |
rs553354474 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601160 | GCTTTGCCCTGTGTC[-/A]ACACTATAAGTTATT | 5607 |
rs553355690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682908 | ACTTTGGGAGGCTGA[A/G]GCAGGTGGATCACCT | 5607 |
rs553358490 | in-del | -/ATG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794935 | TGAAAAGTTAAAACT[-/ATG]ATGATAGGACTCTGA | 5607 |
rs553366507 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768820 | ACACAGTGGCGCTCT[C/G]TGTCATTCTTGGAAA | 5607 |
rs553374032 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705736 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAGAAA | 5607 |
rs553383901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641880 | TAGCAGTTTTAAAGC[A/T]CACTCACAAGAATAC | 5607 |
rs553388492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614308 | TTTATAAACTATAAA[A/G]CACAATAGAATATTA | 5607 |
rs553397078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624208 | GCCAGGCGTGCTGGC[A/G]GGTACCTGTAGTCTT | 5607 |
rs553429216 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546997 | CTTGAACCTAGAGGT[C/T]GAGGCTATAGGGAGC | 5607 |
rs553451863 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621468 | CAAAAGTTAATTAAG[G/T]GAAAATTCAAGAAAC | 5607 |
rs553464020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760725 | GGAGGCCTGTGAATA[A/G]CGGTCTGTGAATGGG | 5607 |
rs553478847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769731 | TAACTCGGCAGCTCC[A/G]TGAGACCTTATGGCT | 5607 |
rs553485444 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578335 | GGGAATGCTCCGTAG[A/G]CAGTAGCCTGAGTTT | 5607 |
rs553494208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567814 | TGTTCTCATTTCCTC[C/T]TCTCATTTTCTAGAA | 5607 |
rs553500584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776448 | GATTCCATGGCTTAT[A/G]TGGGAAAAAGCCAGC | 5607 |
rs553509857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719322 | TTAAGGTACTGTGGC[A/G]TAGAAACAAGCAAAC | 5607 |
rs553519805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654126 | TGAAAGTGAGATATT[A/G]AAGTCTCAAAAACTA | 5607 |
rs553547402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610803 | AAGCATTAAATTTTT[C/T]TAAAAAAACATTAAT | 5607 |
rs553552533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762492 | CTATTTTCAAGAAAT[A/G]TAATAAAACACCAAG | 5607 |
rs553567449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748802 | ACCCTGCAAAAACAG[A/T]CTATCCCGCAGGCTG | 5607 |
rs553598093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607060 | ATGATGTGTATCTTG[A/T]AAATTAAGAGTAGTT | 5607 |
rs553623281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650307 | TCAATTCTGAATGTC[A/T]TTTATTTCCTTTTCT | 5607 |
rs553634508 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664216 | GGGAAGAGTTAGGCC[A/G]GGTGTGGTGGCTTAC | 5607 |
rs553651040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798918 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 5607 |
rs553669816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705835 | AGGAAGCCACCTGAT[A/T]ACAAGCTCAAAGGCA | 5607 |
rs553671813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626388 | AAAAATTAGCCAGGT[A/G]TGGTGGTGGGCTCCT | 5607 |
rs553672644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600955 | ATTTCCGAGTCTGCA[A/C]CTCTCCTGGGTGTGT | 5607 |
rs553675206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805273 | TGAGAAGGTTGGGGG[C/T]GGGCACTGCATCAGC | 5607 |
rs553712887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617844 | CACAGGCATGTGCCA[C/G]CATGCCCAGCTAATT | 5607 |
rs553724868 | in-del | -/T | 0.399968 | 0.200024 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741897 | AAAATAAGAAAGAAC[-/T]TTTTTTTTTTTTTTT | 5607 |
rs553733060 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775275 | TTGTTTAGATATTTT[A/G]TCCCCTCTACTTTGT | 5607 |
rs553733971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607882 | GTATATTGGTTTGGC[C/T]AATATTGCTATACAA | 5607 |
rs553749164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609483 | GATTCTGTAGACCTA[C/T]TCTATAGGTCTATAG | 5607 |
rs553750696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560897 | AAATGATTTTTATGT[A/G]ATCGGTGCCCCCCCC | 5607 |
rs553754595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695030 | AACCAAACACCACAT[A/G]TTCTCACTCATAGGT | 5607 |
rs553758127 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722557 | ATGGGGAAAAAAGTA[A/G]AATCTTAGAGTAGAT | 5607 |
rs553769332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745847 | TGCATTGTGTAACTG[C/T]TAAAAAGTAATTGAG | 5607 |
rs553791312 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679395 | CAATTCAGTGGGGGG[-/A]AAAAATCAGTCCAGC | 5607 |
rs553795070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715676 | CTTGATATGAAGAAT[A/G]AAGAAAGACAAAGCA | 5607 |
rs553809155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583620 | TGTAGACATACTGGG[C/T]ATATTTCCTGTGTCT | 5607 |
rs553826047 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680063 | ACATTTTATATAAGC[A/C]GAAACATACCACATG | 5607 |
rs553828246 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660955 | ATGAGAGAATAGTGG[A/C]GCAACACAATTGCTT | 5607 |
rs553835287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743590 | GAACTCTTTAAGTTA[C/G]TGGTACTAGGCAATG | 5607 |
rs553851787 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746506 | CATGTCATAGGAGAG[A/G]TTATCCAGGCTTTTC | 5607 |
rs553853977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610297 | GTTATGACAACATAA[C/T]TTGTTATTTGGTCTA | 5607 |
rs553857458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602480 | CTACTTATCTGTGTT[A/C]TTTCACCAAACCTTT | 5607 |
rs553858996 | in-del | -/GTC | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639703 | GATCCTCCACGACAT[-/GTC]GTCAGTCTGCTTTTA | 5607 |
rs553871015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709080 | TTGATGGGAAGAATT[C/T]GGCCTGTTTCTCCAT | 5607 |
rs553884296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602618 | ATATTCTAGATGTTG[A/T]CATTTTAATCCTTTA | 5607 |
rs553904355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645742 | TTTTTTTGTAGAGAT[A/G]GGTTCTCGCTATGGT | 5607 |
rs553904592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745360 | ATAGGCATTCACAAA[A/G]CCAACATTTTATATT | 5607 |
rs553909408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716317 | TTGCACTCCAGCAAC[C/T]GAGCAAGACTCTGAC | 5607 |
rs553912692 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701545 | GTAGAGAAAGGTTTC[A/G]CCCTCAAACAGGATC | 5607 |
rs553926758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629506 | ACCAAATTTTCTGCT[A/G]AACAGCAGAAAATGA | 5607 |
rs553929969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700575 | GGGCAGGCCACCTTG[A/G]CTTCAAGTGTGAGAA | 5607 |
rs553941764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566416 | CCTGATCTCAAGTGA[C/T]CCGCACACCTTGGCC | 5607 |
rs553943034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753819 | CAAAAAGCTAAAATA[A/G]AACAATTAAATGACC | 5607 |
rs553950757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575450 | CATCAGCACAGATGT[C/T]TTCACACTGCTTCGC | 5607 |
rs553976522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804171 | GCCTCTGGACAGCAC[C/T]TCCTGCTCTCGGGTC | 5607 |
rs553987796 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545984 | TAACAGGAAACACGA[-/GTG]GCCCCACCACTAGAG | 5607 |
rs553993773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744266 | TAAAATTTGAAGTTT[A/T]AAAAAAAAGAATAAA | 5607 |
rs554003259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559186 | GGGAAAAGTGCCTTT[G/T]CAGTAGTTCTAATTG | 5607 |
rs554043441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638714 | AGCATTCCTTTTTCT[C/T]CACAACCTTGCCAGC | 5607 |
rs554056848 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784244 | CACACAGCCAGGAAA[A/C]ACACAGGACTGTCCT | 5607 |
rs554065826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561740 | AGATTGCTGTTGGCC[A/G]CTGAAGAGATAAAGG | 5607 |
rs554083251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596301 | GCGGCCCATGCCCAG[C/T]TACTTAGGTGGCTGA | 5607 |
rs554111033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751897 | ATAGAGCCCTTTGCC[A/C]CCAGGCTAACATGCC | 5607 |
rs554115940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644334 | GGGAGGCGGAGGTTG[C/T]AGTGAGCCAAGATCG | 5607 |
rs554125488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803666 | TGAATCCCATGCAGG[G/T]CTGATGGGAGGAGGG | 5607 |
rs554167588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782763 | CTGGGGAAGGCAGAT[C/T]GGCAACCCTGGAATG | 5607 |
rs554168160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692720 | CTCTGAGCGAGTTTC[C/T]TTCATCAGAATATGA | 5607 |
rs554187524 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657038 | AATGAATCAGTGATG[G/T]CACAGAGCCAGCTGT | 5607 |
rs554199213 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551425 | GTAACCTTGAACTCC[G/T]GGGCTTACACAATCC | 5607 |
rs554204200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768680 | AAATGAGAATAGATG[A/G]GAATGGAGTCATTTG | 5607 |
rs554214299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589409 | GGTTTACTAATGCAC[A/G]TGGTGTTCCTAGGCC | 5607 |
rs554224752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669648 | AAGTGGTGATTCTGG[A/G]TATATTTTAAATGTA | 5607 |
rs554271140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797628 | AGGTATAGATTTTAT[A/G]TTTATTTTACTTGGA | 5607 |
rs554271282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686158 | CCATATCAATAATTA[C/T]GTTAAGTGTGAATGG | 5607 |
rs554277603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574782 | TGAGACAGGAGAATC[A/G]TTTGAACCTGGGAGG | 5607 |
rs554279001 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692811 | AAACTTCATTGATAT[A/G]CAGCTTTGATATGAA | 5607 |
rs554281913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775770 | TAGAGAGCTTTGAAG[A/G]GGCCATTCCAGGCAA | 5607 |
rs554291493 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676622 | GATAACAATATTAAT[C/G]ATTTTCCTAATATCA | 5607 |
rs554296178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736524 | CTCTGAAAATATATG[A/G]CCATGTCTCACACCA | 5607 |
rs554300328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661896 | CTCAAAGAGAAAATT[G/T]TTATCGTTATGGATG | 5607 |
rs554337175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804416 | TCGGGGATACAACAT[G/T]CCTCAGCAGCAGCAG | 5607 |
rs554337415 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560840 | TTCAAGCTCTAGCTT[C/T]GAGAAGTTGAAGAAC | 5607 |
rs554341625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552245 | CTATAGAAAAATAGT[A/G]CATCTGTCTGAAATA | 5607 |
rs554354123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588850 | AGATGGGATCTCCCT[C/T]TGTTGTCCAAGTTAG | 5607 |
rs554354654 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673859 | TTTGTTTGTTTGTTT[A/G]TTTTTTTGAAACAGA | 5607 |
rs554381870 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612415 | GTATCTCATAAAGAA[C/T]ATTGGTGGAATTGGG | 5607 |
rs554387586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789664 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 5607 |
rs554406120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679234 | TCTGGCCTTTATTAG[C/G]AAGCTTCTGCTTGAT | 5607 |
rs554433786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679352 | TGGGTTGTCTCAACA[C/T]GATACCAATTTCCAC | 5607 |
rs554447937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804773 | CCTTTGTTCTTTAGA[A/G]GGGCACGAGGTCGCC | 5607 |
rs554464143 | in-del | -/GTCTC | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616393 | TGATTTATTTGTCTT[-/GTCTC]GATCAAACTTTTTCA | 5607 |
rs554464340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729689 | GAATGGCTTGAACCC[A/G]GGAGGTGGAGCTTGC | 5607 |
rs554477916 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762581 | AAAAAAAAAAAAAAA[-/AA]CAAGCAGACTAAATG | 5607 |
rs554485220 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738167 | TAGAATAGTCTTATG[A/G]GAGAAGAAGCTATTG | 5607 |
rs554511746 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715487 | TGTGTTCAGAGCTGT[C/G]GGGAACAACCATGAG | 5607 |
rs554515006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759237 | TGATGGCAAGAATGA[C/T]TGCCTAATAATACCT | 5607 |
rs554518516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701421 | CTTTGCCTCTTAGGA[A/G]AAATAGACTAGAAAA | 5607 |
rs554534600 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553458 | AAATACAAAACATAC[C/T]CACAGACAAAATAAT | 5607 |
rs554537107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567308 | TCCACTTCTGGGATC[A/G]CGGCTTTTCCTCTGA | 5607 |
rs554537946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623805 | TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCGAAC | 5607 |
rs554559774 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653603 | ACCCAGCTAAAAAAA[A/T]TTTTTTCATTTAAAA | 5607 |
rs554560043 | in-del | -/TTTAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784050 | TCTTTAAAAAATTGA[-/TTTAT]TATATAGAGAGAAAT | 5607 |
rs554578711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720858 | CTGGGATATAACCCT[A/G]TATTAGGTGAAGATT | 5607 |
rs554597367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629411 | TTTTTTTTTTTGCAC[C/T]ATGCTGTTGATTGCT | 5607 |
rs554606539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709038 | AAAAAAAGATTATTC[A/G]CCTTGACTGATGTAT | 5607 |
rs554608772 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613870 | GCTCACTTTTCAGAG[A/G]TGCATTTACTCTTTG | 5607 |
rs554620812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754680 | TGGAAATACCTTGAT[A/G]TTCACAAAATGAAAG | 5607 |
rs554653792 | snp | C/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751879 | TCGGGCCTCTTGAAG[C/G/T]GTATAGAGCCCTTTG | 5607 |
rs554665748 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772103 | TTTAGCTGTCCCACA[G/T]CGGTTTAATGAATTA | 5607 |
rs554665905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617769 | CGATCATGGCTTACT[A/G]TAGCATCAACCTCCC | 5607 |
rs554688220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582138 | GCAATCTCAGCTCAC[C/T]GCAACCTCTGACTCC | 5607 |
rs554693531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574213 | GTTCCTTGTGAAAGA[C/T]AATGGTGGTCACTGG | 5607 |
rs554707425 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643738 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCTGCAAA | 5607 |
rs554724241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708249 | AATTGCTAGAGCCTA[A/G]GAGTTTGAGGCTGCA | 5607 |
rs554736886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795694 | GTATATATTCTCTAA[C/T]TGTTGAATGCAATGT | 5607 |
rs554749216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759846 | GGTTTTTGTGATGTG[G/T]GATTTCATGGTGCAT | 5607 |
rs554784799 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751809 | GTTTACCTTATTCTT[A/T]CACTGAATTTTACCA | 5607 |
rs554801508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696253 | GGCCAAATTCAATTT[A/C]CTGGAACAATGTACT | 5607 |
rs554802682 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776095 | TCAATTCTTTAAGAG[C/G]CTATTGCAGAAATCA | 5607 |
rs554803239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782392 | CCTAACCATTTTGGG[A/G]GATTGATTTGAGGGC | 5607 |
rs554813237 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773147 | CCTCTTAGATTCATG[C/T]AGAATGAAATTAAAC | 5607 |
rs554838796 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644600 | TGATTGATATTTTAA[A/G]TAAACCATAAAGTAC | 5607 |
rs554864616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721087 | CTACTGTAATAAGCC[C/T]ATTTCTTTTTATTTT | 5607 |
rs554906523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742798 | CAATTACCAACAGGA[A/G]GATTTACTTTGGCTC | 5607 |
rs554938336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605004 | GTAGTACTAATAATA[C/G]AAAAATTATTTACAT | 5607 |
rs554942187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612745 | TTCTTTGCAGAATGG[C/T]AGCTGCAGCGAAAGT | 5607 |
rs555001796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558407 | CCATCATCTCTCACC[A/G]GGATTAGGACAGTGG | 5607 |
rs555006374 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595627 | TTAATTTCATTAATA[C/T]ATTAAATCAAGCACT | 5607 |
rs555014822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601890 | AGCCAAGATGTGAGT[C/T]CTTTCTCCTGAATAT | 5607 |
rs555016035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667631 | ATCATCATTTTCTAA[C/T]GCCGTTCTTAAAAAC | 5607 |
rs555021781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746931 | TCTTGAGAAACTCAC[A/G]GTCTAGGTGAGAGGA | 5607 |
rs555037303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651243 | AATCAAAATTTTTAT[A/G]GATCCATAATATTGT | 5607 |
rs555052560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565722 | TTTCTGAGATTACTT[A/G]GGTCCACTTTTTTTT | 5607 |
rs555093976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740216 | TAGAGTCTAGTATAG[C/T]GCCTGGCATAGCATA | 5607 |
rs555107940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802767 | GGTGCCTGGGTTCCA[A/G]GGAGCTGCACCATGC | 5607 |
rs555114485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633338 | TAGCCAACTCTAGGT[C/T]ATTTACTCCAGGAGA | 5607 |
rs555135112 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556680 | CCTCAGCCTCCCTAG[A/T]AGCTGGGATTACAGG | 5607 |
rs555180103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739106 | GCAACACAGGGAGAC[C/T]CCGTCTCTACAAAAA | 5607 |
rs555182256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747811 | GGAATCCAAAATTCT[A/G]ATTTCTGACTATGAT | 5607 |
rs555189869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699527 | TAGCCTAGCCCTAGT[A/G]TAGATTTACACCCTG | 5607 |
rs555251872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792721 | ATGAAGTTGTAAATC[C/T]GCTCTGTGAGATATT | 5607 |
rs555262585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735958 | GCTAGGTACTCAAGT[A/C]CAAAGGAGGTTCATC | 5607 |
rs555278836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591551 | ATTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 5607 |
rs555281814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588766 | AGTGTCTCTCTTCAG[G/T]TGTTGTACTCAAGTT | 5607 |
rs555289323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788734 | AATTCTAGCTCTTGG[A/G]GGGCTGAGGCAGGAG | 5607 |
rs555325613 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798768 | AATAAACTCAGGAAG[A/G]TTGATTGAAATGACA | 5607 |
rs555345140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587962 | GCTCTCCAGATCACT[A/G]CCACAGCCTCCTGAG | 5607 |
rs555358039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682210 | TCAAATCATTTCAGT[A/G]TTTCTAGAGCTATTT | 5607 |
rs555388413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733228 | TCTGATGTTTATACA[A/G]CCGCCAGCGGAATTT | 5607 |
rs555393940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805716 | GCTCCCCGAGTCTCA[C/T]CATGCAAGCTGCACA | 5607 |
rs555400350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554873 | CTAAATGAGTAATTT[A/G]CGTTTTTGGATTATT | 5607 |
rs555407789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791915 | TTCCCCTCACCACCA[A/G]GGAGAATGTCATGGC | 5607 |
rs555409903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569332 | TGCAATTTATCCAAA[C/T]AACTGATTACACAGT | 5607 |
rs555414881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721726 | TAGAGTTTGTAGGAA[A/G]GAGTTTGTGAAAATA | 5607 |
rs555414905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785775 | GTAAAGCCTGGAGAG[C/G]CTAAGGATGGTCTTT | 5607 |
rs555418725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663839 | ATGATTGCACCACTG[C/T]ACTCCAGCCTGGGCA | 5607 |
rs555441199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736355 | TGGCTTGGTATATCA[C/T]GGCATTTTCTAGACT | 5607 |
rs555467006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694927 | TGGAATACTATGCAG[C/T]CATACAAAATGATGA | 5607 |
rs555467901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800288 | AAAATTAATGCAAGA[C/T]TTCAATATTAATGTA | 5607 |
rs555484696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597125 | AGTGAGCCGAGATCA[C/T]GTCACTGCACTCCAG | 5607 |
rs555488194 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659968 | AATAATTCAGCATCA[A/G]ATACAGGGCTTGCCT | 5607 |
rs555489579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687014 | AACTTTTGAGGTGAT[A/G]GAAATGTTCTGTATC | 5607 |
rs555505399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640811 | ATATTACAAGATATT[C/T]TTAAAAGAAGTTGAA | 5607 |
rs555507031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645672 | GATCCTCCCACCTCA[G/T]CCTCCCAAGTAGATT | 5607 |
rs555508341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806376 | CGCCCTTAAGCACCT[C/T]CCAGGCTAGTGCGAG | 5607 |
rs555529019 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724171 | TTCAGAGAAGATTAC[A/C/G]TACTCTCTTTTGTAA | 5607 |
rs555536569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554199 | TGAGTAGCTGGGACT[A/G]CAGGTGCATGCCACT | 5607 |
rs555550961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656380 | CCCAGGATGTAGTGC[A/G]GTGGCGCAGTCTCTG | 5607 |
rs555555525 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547349 | TGTTGTAGATGCTCA[A/G]TGATGTTTTGGATCT | 5607 |
rs555563104 | in-del | -/G | 0.00394034 | 0.0442113 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692456 | TGGAATTAGTTACAT[-/G]GCCTTTTCTGGTCCC | 5607 |
rs555594222 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574812 | GCGGATGTTGCACTG[A/G]GCCGAGATCGTACCG | 5607 |
rs555597076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738072 | GGCCAGGCTGGTCTC[A/G]AACTCCCGACCTCAG | 5607 |
rs555602558 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612124 | GAGTTAGTTTATGAG[G/T]GTATTTAAATCATTT | 5607 |
rs555612364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688839 | TAAAACCCAGGTCAT[A/G]TGTCTCCTAGCCCAG | 5607 |
rs555627554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790941 | ATTTTACAGAAGACG[A/C]GTCAGAGCTAGGGGG | 5607 |
rs555631526 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730111 | AAGTTGGGGTGCGTC[A/G]TTGCTAGAACCACTA | 5607 |
rs555634568 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648501 | ATTTGGGATAGTTCT[A/G]CTTTATGCATAATTA | 5607 |
rs555641400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724860 | TTCCCAAGTCTTTCA[A/G]CAGCCCAGTGGTGAC | 5607 |
rs555641448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717143 | GAGCAGGAAATCAGA[C/T]AAAGGAAAAGACAGG | 5607 |
rs555666616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625743 | CTGTCATTGCACTGT[A/G]AACCAAACCACATAG | 5607 |
rs555681512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586498 | CAGAGCTGGAAGGAT[A/G]TAACTTGAGGTTCAC | 5607 |
rs555684202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680609 | TTAGCATGACAGAAG[C/G]CTCTTTTAGTAAACT | 5607 |
rs555685033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576656 | GTTACTGCATGTAAC[A/G]GATTATGCAAGGGGT | 5607 |
rs555690569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568823 | CATCCTGACTAACAC[C/T]GTGAAACCCCATTTT | 5607 |
rs555691067 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741599 | TCTGAACCACCTACC[A/G]TACCCTAGAGCTGGG | 5607 |
rs555693599 | in-del | -/GC | | | frameshift-variant, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543344 | ACCTGTAATGCTGTG[-/GC]TAGCCCTTGGCCCCT | 5607 |
rs555709267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762576 | CAGACAAAAAAAAAA[A/C]AAAAAACAAGCAGAC | 5607 |
rs555714791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731045 | TGAAAAGTACAAAGG[A/G]CCACCCATCTGGATC | 5607 |
rs555722390 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547940 | TACCTCTTTGTCATT[A/G]TGATTGCCCCACTTT | 5607 |
rs555724366 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541429 | TTCATAAGAAAGAAA[G/T]AAAGGACGAACCTAC | 5607 |
rs555729614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619181 | AATGGTGTGCCCCCA[C/T]ACTGCTCACATGTAA | 5607 |
rs555744517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585738 | GTTAAAACCCTGGTT[C/T]ATAATTCCCACTTTG | 5607 |
rs555748674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689637 | CATACAGTAGGCTTA[C/T]ATATATGTTAAAAAG | 5607 |
rs555752796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745796 | TACAATGATGTTGCA[G/T]CATCAAATTCTTGTG | 5607 |
rs555777065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67724099 | AAAATTAAAAAGGAC[A/G]TTAAAGCTTCATTAA | 5607 |
rs555792225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544580 | CTACATGTTGCAGCC[A/G]CTTCTAATCTTTCTG | 5607 |
rs555812459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590719 | TTGGCATCCCAAAGT[G/T]CTGGGATTACAGGCT | 5607 |
rs555825640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67672177 | CTTTGGGTATATACC[C/T]AGTAATGGGATGGCT | 5607 |
rs555848037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730293 | GAGGCTGAGTTATGG[A/C]ATAACACCTTCTCTT | 5607 |
rs555871010 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767332 | GCATCATGTTTTATA[A/C]CAGATCTTTATAGAA | 5607 |
rs555876570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783487 | CAACTGGCACAACCT[C/T]TGTGAAGCTTTGCTA | 5607 |
rs555886070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717043 | AGTATTCTGACTCAT[A/G]GATTCAAGTCTGCTT | 5607 |
rs555906166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631287 | TGAATTGCTGTATCC[C/T]GTTAGAATTTTTCCC | 5607 |
rs555918329 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625869 | AATAGGACACCTTTC[C/T]TTTAGAAAAGAGATC | 5607 |
rs555937409 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583886 | TGAGTAGCTGGGGCT[A/T]CAGGCATGTGCCACC | 5607 |
rs555966770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646755 | ATTCTTTTGCACAAT[C/G]TGTCTTTACTTGCAA | 5607 |
rs556010255 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761333 | TTAAACCAGCTTTAA[A/C]TTCCCTTCTGTCTGT | 5607 |
rs556020352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777889 | AAAAAGAAACACAGG[A/G]TGCAGTTTGCAATTG | 5607 |
rs556023275 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610398 | GTGCTAGCAGGGGTG[G/T]TCTATTTCTTGATTT | 5607 |
rs556023812 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762635 | GACAAAGATCATTTC[C/T]ATTCTCTTTTATCCC | 5607 |
rs556040311 | in-del | -/TAAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669277 | CAATAACATACATAA[-/TAAG]TAAGTAAAATACGGA | 5607 |
rs556043206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632028 | TGCCCTTTATCTCCA[A/G]TCTCCTGGCCTTTAG | 5607 |
rs556052042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639851 | AGAATGCTTTCACCC[A/G]TTATCTCTACCTATC | 5607 |
rs556054000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746734 | AGTCAACCTGGGACA[C/G]AGGTTTCTGAAAGTA | 5607 |
rs556070373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799517 | GACAGCTGCCCTGTG[G/T]TCAAAACCAGCTGAC | 5607 |
rs556073856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662742 | TATCTCATTCAACTA[A/G]TTACTCTTAACTCAG | 5607 |
rs556087029 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631565 | CTGACTCCCTCGGCA[C/T]ACTGAAATACCCAAG | 5607 |
rs556096065 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771125 | GAATTCTTAAAACAC[A/T]TGGTAATGTGTACCA | 5607 |
rs556096115 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546779 | CTCATCTATAAGACT[C/T]CTGGGCCAGGAGTGG | 5607 |
rs556117938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610859 | CATGTTGTCTTCTTG[A/G]CCCTAAAATTTCCTT | 5607 |
rs556121782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700779 | TGAAAATTTTTGCTC[A/G]AACACTGCATCACAG | 5607 |
rs556126721 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790049 | AGCCAATAGCTGGGG[A/G/T]TAAACTACAAGAGAG | 5607 |
rs556132791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770521 | GAGACAAAACCAACC[A/G]CAACTCCTTCTTAAC | 5607 |
rs556138629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662095 | ATAAAAATGTATGCT[G/T]TTCTCTTAGAATAGA | 5607 |
rs556143690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553861 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 5607 |
rs556150104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688639 | TGATTACCAATTGAT[A/G]ATGATAATACACTTA | 5607 |
rs556153997 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560965 | TTTACCAAAATATAA[A/G]CACTTGCCCATCCTA | 5607 |
rs556161078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716430 | GAGATCTGAAAGATA[A/T]GAAGGAACCAGTCTT | 5607 |
rs556168212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739062 | AGGCAGGAGACTCAC[G/T]TGAGCCCAGGAGTTT | 5607 |
rs556192351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562124 | GGCATCCTGCTGAGA[A/G]CCTGCCCCTTCCAAG | 5607 |
rs556193990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799030 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGACACCT | 5607 |
rs556194440 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649611 | TTGAATTTTCTTGTT[A/G]TACTTGTTGAAAATT | 5607 |
rs556197961 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576590 | AGATTCCATTAGCAA[C/T]TGCAAAGCTGATTGA | 5607 |
rs556205076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546190 | CCAGGTTTACTTCAT[C/G]TCTTCATCAAGAAAA | 5607 |
rs556210717 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556001 | ATGTTGACCAGACTG[G/T]TCTCAAACTCCTGAC | 5607 |
rs556215987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589527 | CTTTCCATCTATCTA[C/T]TGCTGGTGTTAGAAA | 5607 |
rs556223785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736704 | ACCATGATTCCCTTA[C/T]AATTTTTAAATAATC | 5607 |
rs556233831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791786 | CAAATGCTGGTATCA[A/G]TAAATATAAGCATTT | 5607 |
rs556263154 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682222 | AGTGTTTCTAGAGCT[-/A]TTTTTTTTTTTTTAA | 5607 |
rs556267335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805695 | CCATTCTCTGTCCTC[A/G]CTATGGCTCCCCGAG | 5607 |
rs556272303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803208 | AGCATCACGGATACA[A/G]TGTGCCTCATCAGTA | 5607 |
rs556279138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596355 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGACTGC | 5607 |
rs556282978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603364 | AATTTGCTAGAATGC[C/T]GTGTGTAACGTTAGG | 5607 |
rs556283486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701278 | GTATGAGGAAGTTAT[A/G]TAAGAACTCTCTAAG | 5607 |
rs556295756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730146 | CTTTTGGTGGAGTTG[A/G]CATTTATTTTACAGG | 5607 |
rs556312681 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795793 | CCTGCATTATCTATC[A/G]ATTTCTAAGAGAGGT | 5607 |
rs556315046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546845 | CGAGGTGGGTAGATC[A/G]CTTAAACTCAGGAGT | 5607 |
rs556324907 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605419 | ACTAACTTTGAGAAA[G/T]TCTGCCTTTATATTA | 5607 |
rs556328956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568775 | ACTTTGGGAGGCTGA[A/G]GCGGGCGGATCATGA | 5607 |
rs556350240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694266 | GGAAAAAAAATTAAA[C/G]AGGAAACTTATCTAG | 5607 |
rs556352700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590034 | TTTTAGGCAGCTGTG[C/T]ATTTTTTCCATATAT | 5607 |
rs556359697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654890 | AGTTGGTGAAACCTC[A/G]TCTCTCCTAAAAAAA | 5607 |
rs556365900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745980 | ATAAAACCTGATAAC[A/G]TCTCTCTTTAAAAAC | 5607 |
rs556373276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780801 | TAGCATGAGGATTAC[C/T]GTTCAGAACCAACAC | 5607 |
rs556383405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695081 | ACATGGACACAGGAA[G/T]GGGAACATCACACTC | 5607 |
rs556391835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618711 | TTTTTCTCTCAGATT[A/G]TGTATACCTTTACCC | 5607 |
rs556429339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798304 | CCCACTGTACAGCCT[G/T]CCCAGTCCTATCCAA | 5607 |
rs556449879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554844 | GAAAATTATAAAATG[G/T]ATATGGTCTAAATCT | 5607 |
rs556452320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624894 | GCTTGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 5607 |
rs556457705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631130 | TCAGTTGTAAGCTCC[A/G]TGTATTGTGATTCTT | 5607 |
rs556458493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730944 | TCAGTTTCCTCATCT[C/G]TAAAATGAGGATTCT | 5607 |
rs556462681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723275 | ATGATCTCTCTTTCA[C/T]GCACAGGCACACATA | 5607 |
rs556473555 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591428 | AGCCCAGGCTGGTGT[G/T]CAGTGGTGCGATCTT | 5607 |
rs556486177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686906 | GATTTTTTTTTGAGA[C/T]AGTGGTTAAAACAGT | 5607 |
rs556499491 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723485 | ACACTTCAGACCATT[C/G]TTTTTCAGCCTTTTA | 5607 |
rs556505295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648040 | GTGAGACCCTGTATC[A/G]AAAAACAAATAAATT | 5607 |
rs556508890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797661 | TCACTGGTTTTTTTT[A/T]AATTTGAGAATTCAC | 5607 |
rs556528252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697009 | AAAGAAAATGAGACT[C/T]ACAGTGTACAAACTT | 5607 |
rs556557594 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709331 | GACCCACTAACAAGG[C/T]TGTAAAATTCCTGAA | 5607 |
rs556571383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644430 | AAAACAATTACTCTT[C/G]AATTAGTTTCACTGA | 5607 |
rs556586795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686363 | TGTAATCCCAGCACT[G/T]TGGGAGGCCAAGGCA | 5607 |
rs556587897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544351 | TGGTGATATTTTACA[C/T]TCAGATTTTTCAGAA | 5607 |
rs556603859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752534 | AATACAAAAATGAGC[C/T]GAGCCGGCTGGCAGG | 5607 |
rs556617540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587152 | GAAGGGCGTTTCAGA[C/T]GGAGGGAAGAGGGTA | 5607 |
rs556619496 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680823 | GTATTGTGACAGGAG[A/G]CACATGTTGTGATTG | 5607 |
rs556620191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628263 | GAGGTGGGCAGATCA[C/T]GAGGTCAGGGATTTG | 5607 |
rs556632185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652803 | TCCTCATTCACCCCC[A/G]CTCCCAGCCCCTGGC | 5607 |
rs556637091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741357 | TCCTTGCTGGTTTTA[C/G]CTGGGACTTGACTCA | 5607 |
rs556654970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790417 | TATCATGCAATAAAA[A/T]TACCCTTTTCATATC | 5607 |
rs556665635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793680 | TAAGGGTGTCAAAGT[A/T]TAGTGGTCTATAGAT | 5607 |
rs556665882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697692 | TTTCGTATTAAGAAT[A/C]TTGCTTGTGTTTCAA | 5607 |
rs556678403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592823 | TGTGAAGAATATGCT[C/T]AATCCCTATATGTAA | 5607 |
rs556683114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652118 | CCCTGGTGATTAGTG[A/G]TGTCAAACATTTTTT | 5607 |
rs556727024 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541692 | AAAATGAGCGGGCAC[A/G]GATGGCGCACGCCTG | 5607 |
rs556727529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727403 | CCATTTTTCCCACTA[A/G]TGGGTAGAAAATGGA | 5607 |
rs556742707 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639934 | ACTTTTCTGGATAAG[C/T]CCTGTCACATATGGT | 5607 |
rs556742827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789726 | GTTTCAAAAAAAAAA[A/G]AGGATCTAATCATTT | 5607 |
rs556753777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587445 | AAGATCCTCTGCCTG[C/T]GGTGTGGCGAATGAG | 5607 |
rs556759659 | in-del | -/ATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685565 | AAATGTCTTTAAAAT[-/ATA]ATTATTTAAAGGAAA | 5607 |
rs556774509 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684181 | GTGAAATCCTACAAA[A/G]CTAGACAACCAACTA | 5607 |
rs556800641 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557130 | AGTTTCATTAGCAGA[C/T]TAATGAGTACACCAA | 5607 |
rs556806716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690330 | ACACTTGAAAGCACA[A/G]CCCTGTTCTTAAGGA | 5607 |
rs556820973 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716668 | ACTTCTCTTAGCAGT[A/G]AGGAAGCTGGTCTCC | 5607 |
rs556839738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720373 | ACACACTTACACACA[C/T]ACAAGGAAAAAAAGA | 5607 |
rs556844654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638555 | CGTGTGTCTTTATAA[C/T]AGAATGCTTTATATT | 5607 |
rs556860396 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588808 | ACATTTAAATTTTAA[A/G]ATGTTTTTATTTTAT | 5607 |
rs556873890 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720267 | CATATATATACACAC[-/A]ACATATGCTTATATA | 5607 |
rs556901301 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540959 | TCCCCACGGTACTTC[A/G]AATAAAAGAGACATT | 5607 |
rs556922005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600148 | TGCCTAATTATTGCT[A/G]TATACTAGTTTGTTA | 5607 |
rs556927328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623026 | AGTATGGCGTGAACC[C/T]GGGATTTGGAGCTTG | 5607 |
rs556937014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680126 | TGATGTTTTTGAGAT[A/G]TGTCTGTATTATAGC | 5607 |
rs556956318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778783 | GATAAGTTTCGGTTT[A/T]CTTTGATCCGGGGCT | 5607 |
rs556959497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641717 | ATATTCAAATTCTTT[A/C]CAGTTTGAAACATTT | 5607 |
rs556959635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579454 | CATTTGCCTTAGTAT[A/G]TATTCCAGAGAGTGT | 5607 |
rs556974080 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562514 | TTACTCAAATTTACA[C/T]ATTCTGGTTATGTAG | 5607 |
rs556998390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726903 | TTTGTATGTTTGTTA[A/G]ATTTTATCTTTTTGG | 5607 |
rs557010678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773369 | TTGTTGATTTGACAA[C/T]GCACAAGCTGTTAGA | 5607 |
rs557015423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674349 | GTGCTAGTGTTGAGA[A/G]CACAGTTAACATCCT | 5607 |
rs557019405 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560904 | TTTATGTAATCGGTG[-/C]CCCCCCCCTTTTTTT | 5607 |
rs557036748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741951 | TCAGGCTGGAGTGCA[A/G]TGGCACGATCTCAGC | 5607 |
rs557038620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748684 | GTTTCCTAATGAAGC[A/G]CAATGCCCAACATCC | 5607 |
rs557045872 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546393 | CCTGACACAGATGCC[A/C]GAAGCAGGTTGTAGT | 5607 |
rs557052145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786944 | GGCACAGGCTGAGAC[C/T]GGAGGGAACAAGGAC | 5607 |
rs557068417 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599562 | GAAGTTTAGAGTAGA[A/G]CAAAATATTTAAAGC | 5607 |
rs557069301 | snp | A/C | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720881 | TGAAGATTGTGAACT[A/C]AGCTGCAATAAAGTG | 5607 |
rs557082137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681535 | AATCTTTTAAAATGA[A/G]AAAAGGAGTATTGGA | 5607 |
rs557084907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665649 | TCCTTTTTAATGAGG[G/T]TATCTAGATTTTGAC | 5607 |
rs557093527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642302 | ATCACTTACTAGGCA[C/T]TACTGTGAGTTAGAC | 5607 |
rs557103888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635080 | ATCTTACAGTGGTGT[A/G]TTTTCATTTCCCTCA | 5607 |
rs557105145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628467 | CCTGGGCGACAGAGC[A/G]AGACTCCATCTAAAA | 5607 |
rs557105291 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689158 | GACTCGGGAGGCTGA[-/G]GCAGAAGGATCACTT | 5607 |
rs557117126 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636265 | TACAAAAAATTAGCT[A/G]GCCGTGGTGTCGGGC | 5607 |
rs557127766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806477 | ATGTCACTGCTCGTC[C/T]CTGGGCCTCAATTAT | 5607 |
rs557131909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555558 | TAAATTTCAATATCT[A/G]TTACTGTGTTTGCTC | 5607 |
rs557142628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786592 | CTCGGAACAGTGGCC[A/G]AGGGGCCGTAGTAGT | 5607 |
rs557160275 | in-del | -/GTGT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756559 | TGTGTGTGTGTGTGT[-/GTGT]TGATAACACTTACGA | 5607 |
rs557205561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705280 | ACTCCTGCTATGCCT[C/G]CTGTATAGGCAATGG | 5607 |
rs557212187 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749231 | CTTCATGGTGCTAAT[C/T]TACCTGCCTTTCTCT | 5607 |
rs557234290 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652382 | ATTTTGCAGGCTGTA[A/T]AAGAAACATGGTGCC | 5607 |
rs557242922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635428 | GATCTGCCCACCTCG[A/G]CCTCCCAAAGTGCAG | 5607 |
rs557244190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704153 | CTTATATTAGAAGGA[C/T]ATATGGCTCAGTTTG | 5607 |
rs557249806 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804977 | AACCTCTGCCATCCA[C/T]AGGGCCACACCCAGC | 5607 |
rs557262022 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586483 | TGTTCTGCTTGGTTG[C/T]AGAGCTGGAAGGATA | 5607 |
rs557268841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563756 | CAATGTAGCTGCAGG[C/T]TTAATATGGATACAC | 5607 |
rs557272145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711514 | GAAAAAAGCCATTAT[C/T]CCCTCTCTTTAAAAG | 5607 |
rs557273663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676965 | AGCATTGTACCTGGC[A/G]TATAACAGCTATTAT | 5607 |
rs557318590 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776514 | CAAGAGGGGAGACAG[C/T]GATAATGCAAAGATG | 5607 |
rs557324605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781324 | CCTATTTACAGTTGT[A/G]CCAGCTGGATTTGTT | 5607 |
rs557329038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689485 | AGCCTTAATGATGAG[G/T]TTTTTTTTTCTTTTG | 5607 |
rs557330820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676105 | GCTTCTATCCAACCA[C/G]CCAGCAAGATGCCCC | 5607 |
rs557335415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578256 | CATGGACCTGGTGGC[C/T]GGTCAGGACTGCTCT | 5607 |
rs557336131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599541 | CCTTGCTTTATTCAA[C/T]TGGTGGAAGTTTAGA | 5607 |
rs557340080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801266 | GGCATGTGGAGGTCC[C/T]TTCGGCCTCTCAAAT | 5607 |
rs557351012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732986 | ACAGCGACTGTGGGC[A/G]AATCTGTACTCACAC | 5607 |
rs557390276 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675894 | CTGAAAATGAGTATC[A/G]ATGGAAGCCTTAGAG | 5607 |
rs557398681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606234 | ATCACTGAAAGATTA[C/T]CTTTTATATTATTTT | 5607 |
rs557403642 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543744 | TATAGACACAACCAC[A/G]CAAATGCAAACTGCT | 5607 |
rs557406153 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585442 | TATTCAAACTAGAAT[C/G]TTCCATCGTAGAATC | 5607 |
rs557406208 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592141 | AAAAAAAAAAGGACT[G/T]TCACTAAATTCATCC | 5607 |
rs557418455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740275 | TAAAGTAATTATGTA[A/G]CCCAAGTTTACTTTT | 5607 |
rs557427779 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570812 | TACTGACTGAGCTAC[A/G]TATAATAGGGTATGC | 5607 |
rs557441948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627214 | TTGGCTTCCCAAAGT[A/G]CTGAGATTACAGGAA | 5607 |
rs557444502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620922 | ATAGGTGTAAAGTAA[A/G]TGAATTAGGTGGTAG | 5607 |
rs557472856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682162 | TGTTGTCTATGGCTT[C/T]GAGTGAAGCTGAAAA | 5607 |
rs557494729 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806411 | AGGAAGAGGTGGCAG[A/T]GTCTGAGATGTGCCA | 5607 |
rs557514160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725574 | CATGCTGAGCATATA[C/T]CCAAGTGAATGGCGC | 5607 |
rs557537833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689772 | CCACTTAAGTCAGAT[A/G]TATCTGATTGAAACT | 5607 |
rs557570190 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662871 | ATGCTTTGCACCAGC[C/G]AGACTGGCTTATGAG | 5607 |
rs557577907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640933 | CTAATCACATTTTAA[A/T]GATAACTATTTCATA | 5607 |
rs557578907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613636 | TCCATTGAATGAAAA[A/C]CAAATATTTTTATAT | 5607 |
rs557581537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733248 | CAGCGGAATTTTTTC[A/G]TTTGATTGATGGCAA | 5607 |
rs557598789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696340 | TGACCACACCCATTT[A/G]CTTATATATTATGCA | 5607 |
rs557605157 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570694 | TATAATTGAATTTGT[A/G]GCCATTTGATAGAGT | 5607 |
rs557646991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628073 | AGCCATGAATGCAAG[A/G]CCACGCAAGGTGGAC | 5607 |
rs557696831 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591132 | TGGGCAGATCACGAG[A/G]TCAGGAGTTTGAGAC | 5607 |
rs557707631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757322 | TTTGCAAATCAGATT[A/G]TGTCTTCCCATTGAT | 5607 |
rs557713820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614150 | CAGATCTACTTCCCA[C/T]TCCAGTACTTACAGA | 5607 |
rs557757123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648535 | ATAATGCTACTCTAT[A/G]TATTTGTGTACAAGT | 5607 |
rs557775238 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548131 | CAGTTGGTTGTTAGA[A/T]CTCTGCACTTTGATG | 5607 |
rs557778185 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728211 | TTTTTTCCTGGTCCA[A/G]TACCATGTACTCATT | 5607 |
rs557782225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546076 | GTCAGAAAGGCCTGA[C/T]GAAGGACCTGTGGCA | 5607 |
rs557787088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726617 | TAGAAAGGCAGTTTC[A/G]TATGCAGGAAGGAAC | 5607 |
rs557802808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563693 | AAAAAATTTTTCAAA[A/G]TCTACTTTCAACTGG | 5607 |
rs557809852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692788 | TGTAATTACTACTTA[C/G]GAATAGCAAACTTCA | 5607 |
rs557812728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681403 | TAAATGATTCGTCCA[C/G]TCTCACAGTCAGTAT | 5607 |
rs557820081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655850 | TCTCCCATTAAGCAT[A/G]TGTCCGTATGCTGGA | 5607 |
rs557846648 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603190 | TCCACAGAACTCTTC[G/T]TCTTGTGTAATCGAA | 5607 |
rs557852920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785802 | CTTTCAAAGCTTGCA[A/G]ATCAGTCTATCGTGT | 5607 |
rs557866092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555463 | GGAGGGGACAAATAT[C/T]CAAACCATATCATTG | 5607 |
rs557875789 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680717 | AACCACCTATTATCT[A/G]CTTGGGCTGTCACTG | 5607 |
rs557946539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579270 | AAATACTTGTGTGCC[A/G]AGGACAAGTCATTTT | 5607 |
rs557963394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786517 | AGACTAGACATGCCC[A/G]TTGGCAACATTTAGA | 5607 |
rs557977425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641633 | TGTCCTGGAGGTGTA[A/G]TGGAGAGCAGTGGAA | 5607 |
rs557991965 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682302 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 5607 |
rs558012060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784943 | AGTATCTGAACTGTT[C/T]GTTGTTTTTTCCCTG | 5607 |
rs558022879 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623223 | TGATTGTTTAGTGAC[G/T]TTTCTGCTGAGATTA | 5607 |
rs558032163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663936 | AGTTTTACACACAGA[A/C]GTATAGAAAATTAAG | 5607 |
rs558037952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710660 | AGGCATGCGCCACCA[C/T]GCCCGGCTGATTTTT | 5607 |
rs558065007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718126 | CAGAGGCCAGAAGTA[C/T]GAGAATATCAGCTGT | 5607 |
rs558066376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675489 | CAAGATGAGGAATCC[C/T]CATGGTGATGGAAAT | 5607 |
rs558070526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569675 | AAGTTTGCATCAGAA[C/T]GAGGGATTTATTATG | 5607 |
rs558081856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587081 | TAGATTTAGACTGGG[C/T]GCTGAGAAGGCTCTC | 5607 |
rs558087188 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709961 | TGTGGTGGGTTATTA[C/T]AAACTTTATTAAGGT | 5607 |
rs558087634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673284 | CAGTCCCATCTAAGG[A/G]CATCCTTTTTAAGGA | 5607 |
rs558088997 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748321 | GCTGCTTCCTTTGCA[C/T]GCTTGAATGCCTTGT | 5607 |
rs558096950 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540922 | AGAATATGTATGCAA[A/C]TTTGGCAAATTGAGT | 5607 |
rs558112655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784429 | TCAGCAGAGTGTGCT[C/T]GTGAAGCCAATGCCC | 5607 |
rs558114760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639808 | CTTTCTCACTTCAAC[A/G]CTTTGATTCACGTAT | 5607 |
rs558125591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786878 | TTTATCGTCATTGTC[A/G]TCATCATCACTGCTA | 5607 |
rs558132683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605566 | ATTTATTTTCAGATT[A/G]CTATAGGACAGCTGG | 5607 |
rs558134074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684605 | ATGAAAGACTATAAC[C/T]GGGAAAAAATCAATC | 5607 |
rs558140402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573331 | GCCTCAGGAAACTTA[C/T]AATCATGGCAGAAGA | 5607 |
rs558167140 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580897 | GTTATGTTTCCAAAG[A/G]TTTAAATGCACATAA | 5607 |
rs558185291 | snp | A/T | 0.413582 | 0.189052 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542728 | TCCTCCTCTCGCCGC[A/T]ACCGCCGTCGCCGCC | 5607 |
rs558195759 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794614 | ATTCCACTGAGGGTC[A/G]GGTAACTCTGGAACA | 5607 |
rs558195895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612810 | GATGAAACTGTTCAA[G/T]TAAAGCACAGGCATT | 5607 |
rs558212836 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670071 | TGGTAAATGGAAAAA[A/C]AGACTGTAATACATC | 5607 |
rs558213934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678233 | ATGAAAGAGCATTGC[G/T]GAAGATCCCAGGCAC | 5607 |
rs558214795 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672845 | ATTTTTGTATAAGGT[G/T]TAAGGAAGGGATCCA | 5607 |
rs558216996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585122 | CGTCCCCAAACAATC[A/G]ATCAAAATTGATGGC | 5607 |
rs558217411 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680899 | CCTAGAAGAAGCCTG[C/G]CTTCAGGTGGAGCTG | 5607 |
rs558231493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738127 | AGAGTACTGGGATTA[C/T]AGGCGTGAGCCACTG | 5607 |
rs558246789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636876 | ACATTTGAGTCAGTG[A/G]GCTGGGAGAGGCAGA | 5607 |
rs558249785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632989 | ACAGTTCAGCCATTT[A/G]GGGTCCATAGAATTG | 5607 |
rs558253497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724282 | AGAATGGCCCCAGGT[A/C]TGCCTGTGTGTGAAA | 5607 |
rs558262868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586756 | TAATTAACCTTCATA[A/G]TGAAATGAGAAATTT | 5607 |
rs558264446 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705504 | CTTTGGGAGGCTGAG[C/G]TGGGCAGATCACCTG | 5607 |
rs558272822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677244 | TTTGTTAAGGCTTAA[A/G]AGCTTTACTAGTCGA | 5607 |
rs558275554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692715 | TTAATCTCTGAGCGA[A/G]TTTCCTTCATCAGAA | 5607 |
rs558276940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685139 | TGAACACAGAGCCAC[A/C]CCAAAGCACATCAAA | 5607 |
rs558278200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591331 | GCCTGGGTGACAAAG[C/T]GAGACTCTGTCTCAA | 5607 |
rs558288299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674242 | TGTTGCCATGTGTAA[C/T]GATGAGAGAGCTAGT | 5607 |
rs558295878 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804148 | CCGTCACGACCCCCC[A/G]CCTGCCTGCCTCTGG | 5607 |
rs558303043 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677117 | AAAGAACTTAAAACA[G/T]CTGGGCTATTTTCTT | 5607 |
rs558325932 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702195 | CTCTGTGCCTCATTT[C/T]CCTCATCTGTTAAAT | 5607 |
rs558332593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567276 | ATAGTTTCTTGTAAG[G/T]TATGTTGTTAGAATA | 5607 |
rs558376193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620192 | CTTGACCAACATGGT[C/G]AAATGCCATCTCTAC | 5607 |
rs558381347 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570888 | AAAAAAACAGCATGA[A/G]TATTCCTTATAAGTG | 5607 |
rs558402002 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772597 | AAGAATTGAACATGA[C/T]GTATTTTGAAAACAT | 5607 |
rs558406516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574193 | TGGAAGCCACTTAGG[A/G]GGCTGTTCCTTGTGA | 5607 |
rs558416828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588520 | GATTCTATACTATTT[A/G]AGGGCAGTGACTGTA | 5607 |
rs558421841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664780 | AAAGATGGCTGCTCT[A/G]TAAATGTTATTTTTC | 5607 |
rs558432012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718638 | GCGTGGTGGTATGCA[C/T]CTGTAATCCAAGCTA | 5607 |
rs558437469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707340 | TAGTATGTTAGGAAT[A/C]GATGTAGCAAATCCA | 5607 |
rs558471231 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799728 | ATCTGCCCAGTGGGC[A/C]CACCCACCCAATGTT | 5607 |
rs558488408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655142 | TTTTTATGCTATTAT[C/T]GTCATATAAGTTACA | 5607 |
rs558489581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775561 | CTTGTTCTAGACTCA[A/G]CAGAAGATATAAAGT | 5607 |
rs558502907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628938 | GGAAGCAATTTTGGA[G/T]GTGGTGGAAGCTACA | 5607 |
rs558515713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771675 | GAGGTGCATATGGTT[A/C]TTTATAGGGAAGGCA | 5607 |
rs558517838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620857 | TAACTTCAAAACAAA[A/T]AGATGGAATAAAGGG | 5607 |
rs558519337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622392 | GCAGAGATCAGTGAG[A/G]TAACTAACCAGGGCC | 5607 |
rs558540206 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805485 | GCGGCTCTTTAAGCA[A/G]CCTCTCTAGGGCTGC | 5607 |
rs558546436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765554 | ACATTATAGTTTCAA[A/G]AAAAGAATATTCCTT | 5607 |
rs558549934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735937 | AAGAAGCATGGGAAA[C/G]GATGTGCTAGGTACT | 5607 |
rs558550070 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728166 | AGAGTGATCATTGTG[C/T]TTTTCCTTTGTGTGA | 5607 |
rs558563338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636269 | AAAAATTAGCTGGCC[C/G]TGGTGTCGGGCGCTT | 5607 |
rs558571088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660798 | ATCATCTAATTAGTC[A/G]GTACAAATTTGAACA | 5607 |
rs558582260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715612 | GCACATACTCATATC[A/C]TGTATACACACAAAT | 5607 |
rs558623792 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637261 | TAAATTCCCCTTCAT[A/G]TATACATCTATCCTA | 5607 |
rs558668111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581012 | AAAATATCTAATTTA[C/T]TAGAGTAAATTAAAC | 5607 |
rs558672832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614462 | GAGAGTTTCCTAGCT[A/C]GTCAATCCTCAGGGT | 5607 |
rs558680105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660279 | TAATGCCTCCAAAAT[A/G]TAGTGTTTTTTTTGT | 5607 |
rs558699434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651119 | GCTACTTGAGAGGCT[A/G]AGGCAGGAGAATCAC | 5607 |
rs558699682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623222 | ATGATTGTTTAGTGA[C/T]GTTTCTGCTGAGATT | 5607 |
rs558701056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642425 | TTTTTAGGAGATGAG[A/G]GATGCATGCTCAAGG | 5607 |
rs558711442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794814 | ATGGTTTGTTTCTCC[C/T]TGTTAAGGAACTAGA | 5607 |
rs558712965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719665 | TGACAGAAGAGGAGA[A/G]AAGGAGGAACAATTT | 5607 |
rs558719663 | snp | C/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541843 | GCCTGGGCGACGGAG[C/G]GAGACTCCGTCTCAA | 5607 |
rs558725604 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667336 | ATTAAATAGGTAATA[C/T]ACTTGTTTATGCACT | 5607 |
rs558729978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759200 | GGTATGAAAATAGCC[A/G]GTGCTGGGGGGTGGG | 5607 |
rs558734922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767928 | TTCTCTACTGATGAG[A/T]ATTTTAATTTTAGAA | 5607 |
rs558739114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668527 | CCGACATTACAGGAA[A/G]CATCGCAGCTTCACT | 5607 |
rs558747522 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721451 | TACACAAAGAAAAAA[C/G/T]ATTAGTTACAAGCTC | 5607 |
rs558757819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802170 | CACAGTGGAACATGT[A/G]GCCAGGAATTAGGGA | 5607 |
rs558777606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616788 | TGGTTATTTCTTGAG[C/T]CAAATCCTAACCATT | 5607 |
rs558780094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602724 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCAGTG | 5607 |
rs558788353 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804274 | GTGCACAGCCTAGGA[C/T]GCTGGGTCCCCTCCA | 5607 |
rs558830191 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781401 | TTTGGGGATTGTGAG[A/T]CTTGTGGTTTCGGAT | 5607 |
rs558853268 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742092 | GTAGAGATGGGGTTT[C/T]ACCATGTTAGCCAGG | 5607 |
rs558865033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643532 | GCTCACTGGAAGCTC[C/T]GCCTCCTGGGTTCAC | 5607 |
rs558868264 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711535 | TCTTTAAAAGGAATT[A/T]CCGTTTGAAATGTTT | 5607 |
rs558870086 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748333 | GCATGCTTGAATGCC[C/T]TGTTTTAAACTTAGC | 5607 |
rs558872223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666450 | GGATCTTGATAGACA[A/T]GTTTCAGATGGATTT | 5607 |
rs558877092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579493 | TTTATGCCGTATGTA[C/T]ATAAGTTTTTATGTC | 5607 |
rs558894752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750257 | GAAAAATGTAACTTA[C/G]ACATATATTCCTGTT | 5607 |
rs558901685 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595031 | CTTTAACACTTGAGC[A/G]TAGTTTTTTATTTTA | 5607 |
rs558921675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658937 | ACATTTTGTAGTTAT[A/G]ATTAGCATATGATTA | 5607 |
rs558922450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760060 | ATCTAATACCTTCTT[G/T]GAAAAGTCCAGTGTG | 5607 |
rs558933890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683233 | ATTGTTGATACTTTG[A/G]ATATAAGGTAGAATA | 5607 |
rs558943412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727258 | TGGTTGGATCATTTT[C/G]TTTTTACAGGTGAGG | 5607 |
rs558967755 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681660 | AATTAGGAAACACCT[A/G]AACTTGATATTTTTA | 5607 |
rs558975589 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739957 | CTAGAAACATTACCA[C/T]GTGGTAGGGAGCTTT | 5607 |
rs559012230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558321 | CCATTCATCAGCAAG[C/T]CCTGTTGGCTCTATC | 5607 |
rs559013061 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593112 | TGGCTTAATTTGATT[A/G]GCAGAACAATTTGCA | 5607 |
rs559039005 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571021 | TCCTCTGTACGTGAG[A/T]CTTGCTGCTGAATAA | 5607 |
rs559039461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614997 | AGGGGCTCTGTTTTT[C/T]TTTCTTTCTTTCTTT | 5607 |
rs559039907 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719792 | ATTTTGAGCTATGCA[A/C]ACATTTGAAGAACAT | 5607 |
rs559064940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705901 | GAGAGAGACCAGTGT[A/G]ACTTGACTGGAGTTA | 5607 |
rs559071018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571575 | TTGGAAATGAGAGAT[G/T]CAAGGCACCATTTCC | 5607 |
rs559079820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750882 | TTGCTAGTATATACT[A/G]TTTCCTGTTAGAGAA | 5607 |
rs559086075 | in-del | -/GT | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737572 | TGAAAAAATCAATGA[-/GT]TGCCTAAAAGGAGCA | 5607 |
rs559093632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674923 | ACTATATACCTATCA[A/G]AATGGCTAAAATAAA | 5607 |
rs559095778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587192 | CCTGAGGTGGAGAAG[G/T]AGCTCAGCATGTTTG | 5607 |
rs559107314 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764355 | AAGAAGAAAGTAGGA[C/G]AGCAAAGAAGGTATC | 5607 |
rs559107453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607528 | ATGATGTATTATTGG[C/T]ATCCAGCCAACATGA | 5607 |
rs559133143 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725190 | TTTTCTCTCTGTTGT[A/C]TTGCATGGCATTGTC | 5607 |
rs559134466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572495 | AAGTAAGTTTATTAA[A/G]AAAGTAAAGTGGTGA | 5607 |
rs559138601 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617850 | CATGTGCCACCATGC[C/T]CAGCTAATTTTTTTA | 5607 |
rs559146032 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792083 | GCCAATACCTGCTCA[A/G]TGTGGACAGTATTGC | 5607 |
rs559168870 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557846 | AAGAAATGAAGTTTC[A/C]TTTCCTTAAACTATT | 5607 |
rs559169462 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789482 | CCAGCACTTTGGGAG[A/G]CCAGGTGGATCACCT | 5607 |
rs559172276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692204 | GATGATGGGTGTATT[C/T]ACTGTTGTTGTAAGC | 5607 |
rs559176268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706419 | ATTGAGTGTGGGACA[C/T]CTGAATGCTGTAAGG | 5607 |
rs559233652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698770 | TCGGAATAAAACACA[A/T]ACACATTGCATGATC | 5607 |
rs559270045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594752 | CATATTAAATAATAT[A/G]GCTTTTTTTTTCTTT | 5607 |
rs559289229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557992 | TGCATCCTAGAATTT[G/T]GGGCAAAATAAGAGA | 5607 |
rs559304551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666713 | TACTTTTTCAGTTGG[G/T]GCTGGCCAGCCCAAT | 5607 |
rs559321858 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807297 | CCAGCTCCACTGTCA[A/G]ATGAGAAACAGAAGC | 5607 |
rs559332650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601798 | TGGTATAGAATTTGA[C/T]TTCTCAGGCTTAGAA | 5607 |
rs559344340 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693005 | CCAGTGATAGTGACC[C/T]ATGAGCATGCTGTGA | 5607 |
rs559381393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666072 | TTTGACAAAAGAACT[A/G]AAGGAAAAACATCCA | 5607 |
rs559422022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635140 | TTACATCATCATATG[C/T]GATAAACCCCAAAAT | 5607 |
rs559444088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773412 | TCGAGCATTAGTAAA[C/T]AATAATTATAGTCTA | 5607 |
rs559444169 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765662 | TAAACGTATTTATTG[G/T]CACACTTACTCTGTA | 5607 |
rs559455473 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691185 | AATGTTTATCGAGCA[C/T]TTGAAATATATCTGG | 5607 |
rs559545063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614633 | AGTTTCCTTGATCTC[A/T]GAGGTATTTAGACCA | 5607 |
rs559547412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570993 | TGGAAGAATAATAAG[C/T]AGGCCTGGTATCTCC | 5607 |
rs559547421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800789 | ACACATGCATGTGTA[C/T]GTCCTAAGTGGACGT | 5607 |
rs559547952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649955 | TTGCTGTCTTAACAT[C/T]ATTTAATCTTCCACT | 5607 |
rs559548132 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685696 | GTTTGTACATTATAA[A/G]TGAAATACCCTAATA | 5607 |
rs559557194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698265 | CGATTGCAGCTCACC[A/G]CAACCTCTGTCCCCT | 5607 |
rs559582467 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547604 | GGGATTACAGATACA[C/T]ACCACACATCCAGCT | 5607 |
rs559584451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555809 | TTTTTTTTGAGACGC[A/T]GTCTCACTCTGTCGC | 5607 |
rs559588446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549614 | CCCATTTTGGAGGGT[A/G]ATCAAATTGAAGCTC | 5607 |
rs559603342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706057 | TCACAGTATCACTGA[A/G]TGCTCTGTGGAGCAT | 5607 |
rs559608267 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657318 | CTCCTAGTTTTGAGT[C/G]ATTCAGGTCATTCAC | 5607 |
rs559626058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793829 | AGTAATTAAGGTGGA[C/T]TTCAAACTGTTGAGG | 5607 |
rs559627318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756001 | TGTGGCATTCCCGTT[A/G]ATCCCCATTTTTCAG | 5607 |
rs559634927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758814 | AGTGACAATCAAAGG[A/G]TAAGGTTCCTTACAT | 5607 |
rs559659340 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658403 | ATGATTATGTTTTAG[A/T]TAACATTGGACTAAA | 5607 |
rs559663072 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566646 | AGCCTATATCTCTGC[A/G]TAAGAATAAAAACAA | 5607 |
rs559689945 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591781 | ATTATAAAGCTAGAT[C/G]ACTTAAGAGCTCCCC | 5607 |
rs559698267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802469 | TTTTCCCTTCATTGT[A/G]TCTCCAACTTCTGTG | 5607 |
rs559728240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557086 | AGCTTGACATTCATA[C/T]AGGCCCAGAGACCCC | 5607 |
rs559729218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640409 | GTTAAGAGTTAGAAG[C/T]GTATTTGATCTTTTC | 5607 |
rs559742244 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620350 | CACTCTAGCCTGGGT[A/G]ACAGAGCGAGACTCT | 5607 |
rs559766581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613011 | TTAAAAGAGGAGTTA[C/T]TTACAGAGGCCTCTA | 5607 |
rs559779392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569990 | CAGAATTGCTACAGC[C/T]TAAAAATCAGGTGAA | 5607 |
rs559810844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652908 | TATTGTGTCTGGCTT[A/C]TTTCATTTTGCATTA | 5607 |
rs559811263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806555 | TTACTGGGGAAAGAG[A/G]TCAGATCCAGGCTGA | 5607 |
rs559815426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718439 | CACGTGAGATGGGGT[C/T]TGGGGCAGTTAACTC | 5607 |
rs559823733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764537 | CAGGGCTGGTTATTA[G/T]GGATGTACATCTTAT | 5607 |
rs559831475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612435 | GTGGAATTGGGTTTT[A/G]AAGTCCAAATACTTT | 5607 |
rs559847961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606371 | CCCACAGGATAGAGT[A/C]AGAGTCTGATCTGGA | 5607 |
rs559876622 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674330 | AGGCATTTATGTTAT[A/G]CAAGTGCTAGTGTTG | 5607 |
rs559882971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609667 | CTGTAGACCTATTCT[A/G]TAGGTCTGTAGATTC | 5607 |
rs559885527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747456 | AGGCACTGAAGTGTT[C/T]AGTACTTTAATGACT | 5607 |
rs559891241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711568 | ATTTGAATCAGACTG[C/T]TAATTTGGTTAAAGA | 5607 |
rs559893926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696505 | AGTGAAAGTTGTATC[C/T]GAAACTGAGCACCTT | 5607 |
rs559908363 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755325 | TAGGCTCTTCCCTTA[C/T]TTTTCTCCTCCCTTT | 5607 |
rs559911262 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551397 | CTGGAATGCTGTGGC[A/G]TGATAGCTCACTGTA | 5607 |
rs559919083 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788066 | ATACTTCTCAGCCCC[C/T]GATCTCACCTTGAAA | 5607 |
rs559941704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797879 | GTAGAGACAGGGTTT[C/T]ACCGTATTGGTCAGG | 5607 |
rs559948245 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728570 | GGTTTGAAAATGATT[C/G]CCCAGTTTGTGGGGG | 5607 |
rs559960665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740620 | AGTGTTTCCTTTTCA[A/G]TCTCAGATTTCTTTT | 5607 |
rs559984068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687127 | TTTTTAATGAGATTT[A/T]TTTCAAAAAGTAAAG | 5607 |
rs559985926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679805 | AAGTTGTGTTTTGAG[G/T]TTGATTTTTTAAAAC | 5607 |
rs559988484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752672 | GACAGAGCAAGACAC[C/G]CTCTCAAAAAAAAAA | 5607 |
rs560017851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790574 | ACCCAGAAGTCTGCT[C/T]ATTCTTGTTTTAAAT | 5607 |
rs560028701 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559657 | ATTTTAAGTGACATT[A/G]ACAAAATCTAGCCAG | 5607 |
rs560042145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544655 | GCAGAATAACTGAGG[C/T]ATGGAAGACAGAAGC | 5607 |
rs560055658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638066 | AATTTTTTTAACTTT[G/T]AATTTAACTTTTTTA | 5607 |
rs560066023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741422 | CTTCCTTCACAGACC[A/G]AGAATGGTTATTGGG | 5607 |
rs560088893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742833 | ACACCTATGTGGTGT[A/G]GGACATGAGCTATGT | 5607 |
rs560090644 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582409 | TGGAGAATTTGGGCA[A/G]GTTTCAAAATTCTTT | 5607 |
rs560091869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804091 | CCCTGCAGGCAGAGA[C/T]GCTGCCAGGCTCTGG | 5607 |
rs560095130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634361 | TGACAGAGTAAGACC[C/T]CATCTCAAAAAAAAA | 5607 |
rs560110090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760491 | CACTGAGTGAATTCA[A/G]CCAATAGACCTTATC | 5607 |
rs560138197 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707602 | GAGAGCCCACCTCTG[A/G]TAGAAAAGAAAGATA | 5607 |
rs560180978 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561217 | GCAAAAATGTAAAGT[A/G]CTTTCATGTGTGGTG | 5607 |
rs560188810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696735 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG | 5607 |
rs560200406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700159 | TCGTTGTAAACAGAC[A/G]GTTCTGGAGTTAGTT | 5607 |
rs560224020 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715176 | CTCATTCCCCTGCTC[C/G/T]TACTCCCTTTTCTGT | 5607 |
rs560256890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643401 | GGCAGTTTTGTATTA[C/G]ACTTACAGTCTAGTT | 5607 |
rs560275414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787169 | CTGATTCCGCCTGCC[C/T]CTGGTGGGCCAGACC | 5607 |
rs560281011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699013 | TATCTTTAACCCAAG[A/G]TCTCAGAGTTGGCAC | 5607 |
rs560293327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623501 | ATTTGTAGAGCATAT[A/C]GTCTAACTAGCACGT | 5607 |
rs560294640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708515 | CTTTTTTTTTCTAGA[C/G]ACGTGGTCTTGATAT | 5607 |
rs560314389 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794056 | ACAGTGGAAATAGAC[-/TT]TGGTTTCATGAGGCT | 5607 |
rs560316972 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603052 | GTTAATGTTGTTTTT[A/C/T]AAATTGTTATTTTAA | 5607 |
rs560331464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575374 | GGAGGTGGCGGGGCG[C/G]GGGAGGGCAGTGGGG | 5607 |
rs560356462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588025 | CCCTCCTCCACCCTG[C/T]AGCTGGAGCCATCTT | 5607 |
rs560383281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729825 | GCACATGAAAGCTGT[C/G]GTCAAATTTGAGAAG | 5607 |
rs560398930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744578 | TCTAAGTTACATAGG[A/T]AGATTCATTTTAGTT | 5607 |
rs560399801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783128 | TTTCAGTCTGCACTC[A/G]CCATTTTTATGTCTT | 5607 |
rs560400502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659917 | CAGTTCTACTGGAGT[A/G]GGAAGACTGTTGAAG | 5607 |
rs560415846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594993 | CCACTTGATAGGGAA[A/G]ATAAAAGTCACATTT | 5607 |
rs560430818 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623884 | TTACAGGTGTGAGCC[A/T]CCGCCCCCGGCTACT | 5607 |
rs560453596 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767664 | AAAACAGGCTGCAGC[C/T]GAAATTGATATCATG | 5607 |
rs560488045 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543088 | CGCTAGTTCCTGCGG[G/T]CCTTTGCCCGCTTCC | 5607 |
rs560488171 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798253 | CCCTCTGGGCATCTG[C/T]GTGGCCCAAAACTGC | 5607 |
rs560491564 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796419 | CAGGAAGTTTAAAAT[A/C]ATGGCAGAAGGCAAG | 5607 |
rs560500759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782442 | TCTTGTTTACACTTT[A/C]AAACCCCTGTGATAT | 5607 |
rs560505578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635929 | GTTTACATCTTTAAT[A/G]TCTCTACTTAACATG | 5607 |
rs560538339 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594076 | TTAGAAGAAATGAAG[C/T]TGATCTGCTTCTGAC | 5607 |
rs560542450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729537 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 5607 |
rs560555532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667952 | TGAGCAATAAGCAGC[A/G]GCAAACCACTCATCC | 5607 |
rs560566941 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610700 | GTGAAATATGTTTAG[G/T]TTCTGATTTGTACAC | 5607 |
rs560568432 | snp | A/G | 7.07526e-05 | 0.00594738 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642502 | AGGACTTTGAGGTGA[A/G]CTTCATGGAGACAAT | 5607 |
rs560577352 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617024 | GTCCTTCATAGAACA[A/C/G]TGGCAATACTATCAT | 5607 |
rs560601380 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690830 | TGAGCCACTGCTCCC[A/G]GCCATGTATTAGTAA | 5607 |
rs560602746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684145 | TGCGTCTGGCCTAAC[A/C]TCAGCCTCTGCATTT | 5607 |
rs560609946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699188 | AAAGACAGTGGGCTA[C/G]TCCCAGGACAATTTT | 5607 |
rs560623915 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645432 | GCAGTGAACCAAGAT[C/T]GCCCCACTGCACTCC | 5607 |
rs560666520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678552 | TAGAAGTTGGAGATA[C/G]CAACAGCACCTGATG | 5607 |
rs560687622 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675277 | GCAATAGAAAGGAGC[A/G]AACTGTTGATGCCCA | 5607 |
rs560696055 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721176 | GGTACATGTGCAGGA[A/T]GTGCAGGTTTGTTAA | 5607 |
rs560745265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677557 | TTTATGCATATAATG[C/T]GGTATTCCTTTGTTT | 5607 |
rs560757851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581337 | TATCTCCAAAAATAT[A/G]AGCTGATGAGAGTAA | 5607 |
rs560761869 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782345 | TTAAGGCAAATCTGC[C/T]GATGTAAACAAAATT | 5607 |
rs560771792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623314 | CAAGAGATAAACATG[A/G]TAAGAAATCTAGAAG | 5607 |
rs560783723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728523 | TTTTTATTATAGAAG[G/T]GTACCAGCACTAAAA | 5607 |
rs560793955 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634284 | TAAGGTGGGAGGATC[A/G]CTGAGCTGAGGAAGT | 5607 |
rs560801671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573410 | GGGTAGAGGGTGGGG[C/T]GGGAGTTGCCACACA | 5607 |
rs560819356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589071 | GCTAGTCTCAAACTC[C/T]TGGCTCAAGCAATTT | 5607 |
rs560819452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559543 | ACTCTGCCATTTTGT[A/G]TATTTGTGACACACT | 5607 |
rs560819653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760202 | GACATTAACATTCTA[C/T]CAAAACACAGCAGTA | 5607 |
rs560822877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550725 | TGAAGTAAGAACTGT[A/G]GTTTTTTTTTTTTAA | 5607 |
rs560823425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714813 | GAGCATTTAGGATTT[C/T]AGGTTTTTGGATTGG | 5607 |
rs560853582 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797831 | AGGATTACAGGCATG[A/C/T]GCCACCACACCTGGA | 5607 |
rs560854221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768048 | TTCTTGTAGCCTCTT[C/T]GGTGTTTTTTGTTGT | 5607 |
rs560854673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730036 | CAAATTGTTACTTCT[A/G]TCTGAAATAATAGAA | 5607 |
rs560857164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616414 | ATCAAACTTTTTCAT[A/G]ATGAATCAGATCTCA | 5607 |
rs560886139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693075 | CACGAAGACCAAAGC[G/T]AAGGTCATCGTTGTA | 5607 |
rs560888152 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584062 | CCATAATTCTGATGT[A/G]ATAACATGTTCTCCT | 5607 |
rs560889951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668059 | GAAGCACAGCAGTTG[C/G]TATTCATAATGGATC | 5607 |
rs560893303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721053 | GTGAATTACTGTTGC[C/T]CTCTTCCTGTTTAAG | 5607 |
rs560901984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641982 | GTTATTTTAAGGTGG[G/T]TTCTACTTTCCCTCT | 5607 |
rs560912988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750319 | GGGAAATGAACATTG[C/T]CTTTGCTAAAACCAG | 5607 |
rs560914115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615528 | GATTTCCCTGAAACT[A/G]TTTGAAGTATTTCTG | 5607 |
rs560923987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609633 | GATTCTGTAGACCTA[C/T]TCTATAGGTCTGTAG | 5607 |
rs560941890 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652208 | TGGTTCTGAGGTTTT[C/T]GGGGTGTGTCATTAG | 5607 |
rs560963581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767353 | CTTTATAGAAAGCCA[C/G]TCCAGAATTTTAACC | 5607 |
rs560981362 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562007 | TTTGTCTGAGGTTCT[C/T]CAGGCTTGGGATCAG | 5607 |
rs560985380 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609034 | GTGACTCTGGGAAGT[G/T]GTGAACTCCTCTACC | 5607 |
rs560990723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789795 | TTCTTTCATATGTTT[A/G]TTGGTCACATTTTTT | 5607 |
rs560994352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602364 | TAATGCCTTTATGCT[A/G]ATAGCCAAATATAAT | 5607 |
rs560997067 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691287 | TCAAATGTCAGTTAT[C/T]AGGCTAACTGAGGCT | 5607 |
rs561018822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651484 | ATTCTTTCTATCTGA[C/G]TGTACTTTTTTACCC | 5607 |
rs561037859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642473 | GGGCCAGAGCTAGAG[A/G]TGAATTTTGATGGAG | 5607 |
rs561042432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635254 | GCAGTGGTGCGATCT[C/T]GGCTCCGCCTCCTGG | 5607 |
rs561058789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595970 | GCATCTCTAAAGTTA[C/T]TTTTTCTTTTTTTTT | 5607 |
rs561076168 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710189 | TAGCATATGCATAGC[A/T]TACGCATTTTGCTCT | 5607 |
rs561076176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759403 | ATCTCTACAAAAAAA[A/C]ACAAAAATTAGCCAA | 5607 |
rs561081908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650562 | AAATTTTGTCAAATG[C/T]CTGTTTTATATCTAT | 5607 |
rs561091180 | in-del | -/ATAGA | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609704 | CTATTCTATAGGTCT[-/ATAGA]ATAGAATAGACTTTG | 5607 |
rs561101950 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705983 | GGCAAATATAGCCTT[G/T]TAGGCCATGCTAAGG | 5607 |
rs561116471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794019 | AGAAGGAAGCTTGCA[A/G]CTGAATAACTTGTCT | 5607 |
rs561117719 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708763 | TCTTGCCACACTCTT[G/T]CATAAAAGATGATGC | 5607 |
rs561120367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549945 | GTTTCAAAAATCTTT[C/T]CCAGGTTCTCATATT | 5607 |
rs561131125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780892 | TGATCAGCAGCACAT[A/G]TGATCTTTGGTATGC | 5607 |
rs561131952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782550 | CTCACAGTGACCAGG[A/C]CTGAGTTTATTCAGC | 5607 |
rs561133070 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641585 | ATTCAGTCACTTGAC[A/T]GCTTATATTTAACTT | 5607 |
rs561133487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595233 | GTGATATAAATATTT[A/T]TTTCTTTTCTGTCAC | 5607 |
rs561147338 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774847 | CATGGGCTGCATGGG[C/T]CGCTTCAAATGTGAG | 5607 |
rs561193750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593767 | AATAAAAGACTCTTA[C/T]TGATTTTCTTAACTG | 5607 |
rs561194538 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662268 | AATTGGCTTTCTCCC[A/G]TTGCATTTCTTATTT | 5607 |
rs561208701 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685908 | CCTATCATTGCATTT[G/T]CACTACATCAGCAGA | 5607 |
rs561217929 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683495 | GGCGGGGTGTGGTGG[C/T]TCATGCCTGTAGTCC | 5607 |
rs561241315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789090 | ATTGTTAATAGTAGC[C/T]TGGGTATCCTTCTAG | 5607 |
rs561251222 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750642 | ATCTACTAGTTTCTC[A/G]GGTAACTCTCTGCAC | 5607 |
rs561259177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601142 | GACCTTATAAATACC[A/G]TTGCTTTGCCCTGTG | 5607 |
rs561263910 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740001 | ATGGGGGGAAGCTGT[C/G]TTAGAAATCTATAGA | 5607 |
rs561266872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697410 | CTAAGTGACTTACCC[A/G]AGTTCACAAAGCTCA | 5607 |
rs561270174 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543279 | TCTTGGAGCCCCCTC[C/G]TAACCAGCGGCCAGT | 5607 |
rs561281684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735364 | TGGCCAGTTAGGTTC[A/G]TGATTCCTGTGTTGT | 5607 |
rs561288522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718706 | GAGGTGGAGGTTGCA[A/G]TGAGCCGAGATCATG | 5607 |
rs561295063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781621 | GTATCGTGGTTTACC[A/G]TTTCTCTGGTCTCTT | 5607 |
rs561295671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801609 | ACTCTGCCACTTTCT[C/G]CATGACCTTGCCACA | 5607 |
rs561299063 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597234 | TAAAAAGCTCTCCTT[C/G]ACCTCTTTTCAATTT | 5607 |
rs561307824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787843 | TGCATTGTCTGTCAT[A/G]TATTTAAACTGTTTA | 5607 |
rs561330896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600473 | TAATGAAATGACCCA[A/G]GCAAACAAATTGTCA | 5607 |
rs561334755 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541298 | GAAAATGACCAACAT[C/T]AATTTTTTTCTCTCA | 5607 |
rs561349090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745643 | TTTCTGGTGGAATTA[A/G]CAGAGGAACATAATA | 5607 |
rs561350912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649857 | CATTTGAATTTTAGA[A/G]TCAGCTTGGCAATTT | 5607 |
rs561380475 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542098 | TATTTTAGGGCACTC[C/G]TGCGGTAAAGAACTT | 5607 |
rs561403113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690643 | GGTTGAAGCAATTCT[C/T]CTCCCTCAGCCTCCC | 5607 |
rs561414061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742134 | CTGCCCTCGTGATCC[A/G]CCCGCCTCAGCCTCC | 5607 |
rs561424846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738304 | TGAGGCGACCTGGAC[C/T]CCAGGCCTAGTTGGT | 5607 |
rs561440316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639530 | AACATAGGTAGTCTT[G/T]TTCTAAGTGCCGGTG | 5607 |
rs561450218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684735 | GAATTCATAGGAAAC[A/G]TGAGCATAATGAGAG | 5607 |
rs561505244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628711 | AGTTAGGAAAGCCCT[A/G]TTAAAGCAAGAGATG | 5607 |
rs561511100 | in-del | -/ATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590820 | TACTGCCACCACAGT[-/ATA]ATAATAACCAGAGCA | 5607 |
rs561521671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684116 | GAGCTCTAGAAATTG[C/T]ATAGGAGTTCCCTTG | 5607 |
rs561523046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597581 | ATTCCATAAGCTTCT[A/T]AATAGCACTTTCTTA | 5607 |
rs561551203 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572712 | ATTATTATTATTTTT[A/T]TTTTTGAGATGGAGT | 5607 |
rs561568180 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652653 | GGACAAATATTCAAA[C/G]TGTATCAGCCATTTT | 5607 |
rs561576807 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552683 | CTCAAGTGATAGTCC[C/T]ATCTTGGCCTTTCAA | 5607 |
rs561578902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632500 | GAAAGCTGAATTGTC[A/G]AAGATCACAGAGTTG | 5607 |
rs561633096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791214 | ACTTTGAAGCTTTGG[A/T]AGAGGAGACTCTTCT | 5607 |
rs561653347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676464 | CAAGCAGAATGGACA[A/G]ACAGCTTTAGCAGTT | 5607 |
rs561656709 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755970 | CCTCTTTCCATTGTC[C/T]TCCCCACATCCTCAC | 5607 |
rs561657815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626719 | ACTTGGGCAACATGG[C/G]AAGACTTCATCTCTT | 5607 |
rs561664663 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694750 | TTGACCCAGCCATCC[C/G]ATTACCAGGTATATA | 5607 |
rs561681515 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646983 | TTTTTTTATTCATTT[A/C]TATTTTGGTAGTTCT | 5607 |
rs561689639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737877 | TTTTTTTTGAGACAG[A/G]GTGTCACTCTGTCAC | 5607 |
rs561695235 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805346 | CTGACCTGTGGTCCA[G/T]AGGGGCCATGCCGTC | 5607 |
rs561695239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584060 | GGCCATAATTCTGAT[A/G]TAATAACATGTTCTC | 5607 |
rs561722107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546338 | AACCCCACAGGGGGA[A/C]AATACCTTGCTAAAG | 5607 |
rs561739543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553461 | TACAAAACATACCCA[C/T]AGACAAAATAATGAC | 5607 |
rs561752376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569129 | TGTCCATTTAGAAGT[A/T]GAATATTTAATAGCA | 5607 |
rs561753434 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589603 | AAGGCATTCTATAAA[G/T]GCAATGAATCAAAAT | 5607 |
rs561783669 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598003 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCCGGATA | 5607 |
rs561801193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687339 | AGCCAAGCTTAGGAG[C/G]TATTTATTTGCATAA | 5607 |
rs561802851 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695116 | GACTGTTGTGGGTTG[G/T]GGGGAGGGGGGAGGG | 5607 |
rs561818976 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576963 | AGACGGAGTCTCGCT[C/G]TGTCGCCCAGGCCGG | 5607 |
rs561819068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724422 | ATTTTTTGAGTTAGG[A/G]TCTCACTCTTGCTCA | 5607 |
rs561823534 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661162 | AGAGTTTTTTTTTTC[C/T]CCCAAAGGAATTTAT | 5607 |
rs561828932 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653626 | ATTTAAAATGAAACC[A/C/G]ACTTTTGGTTTCTTT | 5607 |
rs561844372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619927 | AAGTAAAATTTAGCT[A/G]GGCATGGTGGTTCGC | 5607 |
rs561864967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722750 | TGAGTGTTCCAAAGT[A/G]GCTGCTGCATTTCTA | 5607 |
rs561872607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732250 | TAATGGTGGGCAATG[G/T]TTTGTTTAATGACAC | 5607 |
rs561882348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673037 | TCTCTGTTTTGGTAC[C/T]AGTACCATGCTGTTT | 5607 |
rs561897305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785104 | CACATGAACAACACT[A/G]TGGCTAATTTTTGTA | 5607 |
rs561933652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610500 | GCATATTGCACAAGC[A/C]AATATTTGTGTACCA | 5607 |
rs561940310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649354 | TCACTTTCTTTTTTC[C/T]TTTCTTTTCCTTTTT | 5607 |
rs561951023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686458 | CTAAAAATACAAAAA[C/G]TAGCTGGGGGTGGTG | 5607 |
rs561969826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723311 | ATATTTGTTATTTAA[A/G]TTATAAAATCCAACA | 5607 |
rs561978415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717644 | CCTAGCAAGGCCCAG[C/T]CATTCTATGTAGCAT | 5607 |
rs561978931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736761 | AAGTTAATGAACTTG[A/G]TGTTCAGTCTGGCTT | 5607 |
rs561987649 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564264 | CTGCACAGGGCCATT[A/G]TAATGATCAAATAGA | 5607 |
rs562000797 | snp | C/T | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686332 | AATTACATGGCCAGG[C/T]GCGATGGCTCACACC | 5607 |
rs562002313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604625 | GGTTGGGCGGGGTGC[A/G]GTGGCTCACGTCTGT | 5607 |
rs562014043 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698568 | CAACTATTCAGTCTT[-/C]CTGGCTTACTATCAT | 5607 |
rs562033003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753952 | AAACGTAGAAAGAAT[A/C]CAGAAGTTCACATTG | 5607 |
rs562039854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783064 | GCAGAAGCCTTTTCT[A/G]CTGTTGTGAGACATG | 5607 |
rs562048053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624281 | GAAGCGGAGCTGGCA[C/G]TGAGCCGAGATCGCG | 5607 |
rs562063548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611053 | AATGTATTTGGAAGA[C/T]ATGTATTGTGTGAGG | 5607 |
rs562070848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574494 | GGAGAATCACTTGAA[C/T]CCAGGAGGCGGAAGT | 5607 |
rs562081453 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696200 | ATTTTGAGTTCTACA[C/T]GAGCCCTATGCCAAA | 5607 |
rs562112479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753915 | ACATGAACATTCATA[A/G]CGGCATTATTCATAA | 5607 |
rs562123675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678737 | TTGGGAAGCCGAGGC[C/G]GTAGGATCATGAGGT | 5607 |
rs562148631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670245 | AAAGGCAGAATACAT[A/G]CATGGAAAAAGCAAA | 5607 |
rs562149957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752711 | AGAAAGAAAGAAATG[A/G]AAAGACATTTTGTGT | 5607 |
rs562151523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729479 | GAGTCTAAGAAATGG[A/G]TTTTGCCATGGCCAG | 5607 |
rs562163811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769287 | AAGACCATTTGTGTG[C/T]TACTTAAATAATCAT | 5607 |
rs562171848 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595186 | GACAAGTTAGAAATA[A/G]CTTTCTGCCTGGGTT | 5607 |
rs562197076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666580 | GTAGGTCCTTCTTTT[C/G]ATCCCTGGTTGCAAC | 5607 |
rs562203678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776049 | TGTTCATGTATAGGG[A/C]GGTCCCTCATCCTTG | 5607 |
rs562213418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790699 | CTCTACTGCAGCTGT[C/G]AGGAGAGCCAGTCAC | 5607 |
rs562224535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653840 | TCTAAGCACGGCTTT[A/G]GTTGCATCCTAGAAG | 5607 |
rs562231920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645885 | TATATTGGTTTGAGG[A/G]TCATTCCTATGCTCC | 5607 |
rs562243340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638134 | ATAAGTATACTTGTG[C/T]CATGGGGGTTTGTTG | 5607 |
rs562245742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709205 | TGGGATTTGTGTGGG[C/T]TCACTCTGTATTGGG | 5607 |
rs562251144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790056 | AGCTGGGGGTAAACT[A/G]CAAGAGAGTCGTTTT | 5607 |
rs562266741 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725342 | TGACCACTTGCAACC[A/G]GAAGCTTTGTGTTGA | 5607 |
rs562270327 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722949 | ATTTGTAGTTATGCC[A/G]AGAAACATAGAATAT | 5607 |
rs562270483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552735 | AGCCACTGTACCCAC[A/G]AAGTACTTAAAAGGA | 5607 |
rs562276631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561174 | TCAGTTTAGCCTACA[C/T]TTAAAGAGAATTTGA | 5607 |
rs562282376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761969 | GTTGACCTGACCAGT[A/G]TATGAAATTCAAACA | 5607 |
rs562292032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769860 | CACAAAGGGTCATAA[G/T]CATACTTCAGAGCCT | 5607 |
rs562299379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708746 | GGAGTCATAAAAAGG[C/T]CTCTTGCCACACTCT | 5607 |
rs562300582 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702934 | TGCAAATAAGTGATA[A/C]TATCATATAATGTTG | 5607 |
rs562330844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783928 | AGCCACACTAGCCAG[C/T]ATTCATACTACAATT | 5607 |
rs562335240 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764882 | TCTCCCTTATACAAG[C/T]AGAGTTCTGCTAAGA | 5607 |
rs562343437 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793748 | CTGTATAGAAAATAT[A/G]CTCTTTGATCACGTT | 5607 |
rs562347522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762462 | GATTAACCTATTTTC[C/T]ATTTCTCCACTCACC | 5607 |
rs562356990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653043 | TATATACTGGTTTAG[C/T]CAGATTTTTTATTTT | 5607 |
rs562367874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638806 | TGTGGTTTTGATTTA[C/T]GTTTCTCAAATGATC | 5607 |
rs562383702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804884 | GCAGCCGTGGGGTGG[A/G]CATATATATGGGGAG | 5607 |
rs562396320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694585 | CACCAGTTAGAATGG[C/T]GATCATTAAAAAGTC | 5607 |
rs562404884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778023 | GCTCTTGGATTTTTT[C/T]CCTTCATGTCATCCC | 5607 |
rs562406942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680803 | CTCACTGAAGGAGTG[A/T]GACAGTATTGTGACA | 5607 |
rs562406944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790987 | AGAGAATGAAATCCA[C/T]AGGACTCCTGGAAAC | 5607 |
rs562450777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798460 | CACCATGGCCCACTG[A/G]AGTCATCCTGTGCCC | 5607 |
rs562459139 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700717 | AATCCCTATCCACCT[G/T]AAGAGTTGTTTAGGA | 5607 |
rs562465622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709154 | GTTCCCCTCCTGTGG[A/G]TTAGTTATGGAATCA | 5607 |
rs562465956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701082 | CTTTTGTGTGTGTGC[A/G]TGTTTTTTCTGTATT | 5607 |
rs562468575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680245 | GGATATTTGGCATTG[C/T]ATCCACTTTGGGACG | 5607 |
rs562492804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784477 | CAACTCCCTCCCTAT[A/G]GTCCCTTCCACCTTG | 5607 |
rs562502674 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583970 | CCCAGGCTGGTGTCA[A/G]ACTCCTGAGCTCAAG | 5607 |
rs562504289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708630 | CTGCACCTGGCTGAA[C/T]GCCTTCATTGTTTTA | 5607 |
rs562513894 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736123 | AAGGAAGTAAGAAAA[A/G]GGAGGGGAGCATGGT | 5607 |
rs562515728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728588 | CAGTTTGTGGGGGAA[A/G]TAAGTGAAATGTCTA | 5607 |
rs562532480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687294 | AAGTCTGGAGTAGAA[C/G]ACAAAAAGCTGTATT | 5607 |
rs562544777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595888 | CTCATTAGAAATAGC[C/G]CAAAGTGTCAATTTG | 5607 |
rs562546412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588219 | ATCCCACCTGACATT[C/G]CAGCTTTGCTGATGA | 5607 |
rs562561513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576131 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 5607 |
rs562563553 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577922 | GGAGAATTGCTTGAA[C/T]CTGGGAGGTGTAGGT | 5607 |
rs562566522 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557781 | TTAAGAATAGTTGGG[A/T]GGGAGCCTCTTTTTG | 5607 |
rs562581286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701664 | TGACTGGAGCTAAGT[A/G]TACCAAAGAATCACC | 5607 |
rs562603667 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605796 | CCCTTGGTACGTCTT[A/G]GCTAAAATGAGAATG | 5607 |
rs562618373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693704 | TCAATCTAGTCATGA[C/T]CTGATTTTTAAATCT | 5607 |
rs562626361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730754 | CAGGGAATTGCTGCT[C/G]TGAACCTAAAGTCTA | 5607 |
rs562657397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738165 | CCTAGAATAGTCTTA[C/T]GAGAGAAGAAGCTAT | 5607 |
rs562684183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791070 | AGTCCACCTGTGAGA[C/T]ATCCGAGCTGCAGCT | 5607 |
rs562719325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617093 | TATACATGCAATTAC[A/G]CTCCAGGTCTTTTCT | 5607 |
rs562746498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743698 | CAAGTTATAATGGAT[A/T]GGAGGTTGTATGTCC | 5607 |
rs562781653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623897 | CCACCGCCCCCGGCT[A/G]CTTCCTACCTTCCTA | 5607 |
rs562786676 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723584 | ACTTTTTAATTTAAC[A/G]TTAAATAGAATCCCT | 5607 |
rs562786852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731360 | CCTGGGAGCAACATA[A/T]AGGTTAAAGGGCTGG | 5607 |
rs562806066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798452 | AGCCACCTCACCATG[A/G]CCCACTGGAGTCATC | 5607 |
rs562813675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632451 | AAAATTACATAGTAA[G/T]CCTGTCTACTTTAGA | 5607 |
rs562828191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687918 | TCTATGTGTAGAAAT[A/G]GAGCGTGTTGATGGA | 5607 |
rs562837475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761115 | CCTGGAAATGGAAGC[A/G]TCTGGGCCCACGAGA | 5607 |
rs562842981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629637 | GCAGGTGAAGATGAG[C/G]AATTCCTGAGGCACT | 5607 |
rs562850537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777272 | ACTTGAACGGGGAAG[A/G]TGTGGGCTGTGGGCA | 5607 |
rs562850723 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603805 | AATGGTGTTGATGAT[-/A]AAAAAATATGGTTTT | 5607 |
rs562851852 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781981 | TTGACAGCATTTGAT[C/T]ATGACAGTAACTTTA | 5607 |
rs562857738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788997 | AAAAAAAATTACACA[A/G]TACAGAAGGATATAC | 5607 |
rs562862109 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773553 | CAGTTTAGAGGTTTT[C/T]GTCCTTTGTATTCCA | 5607 |
rs562864932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629161 | GAAACAAAGCGTAGC[A/G]AAAGAGGAGAGCTAG | 5607 |
rs562871661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685441 | AGCATTACAAAAAAA[A/T]GTTAAGCTATTTAGG | 5607 |
rs562874238 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770996 | AAAGCATGCCATGTC[A/G]GAAAAAAGCATACAT | 5607 |
rs562893539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684942 | TTAAATGAGCACAAC[A/C]TTAATGATCTTTGAG | 5607 |
rs562901133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722634 | AGATGATTTAAACTC[C/T]TTCTCTAGGACTGTG | 5607 |
rs562908173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643926 | TCAGTATGATTGTAT[A/G]TATATTCTTCAGTTG | 5607 |
rs562926233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636553 | TTTCACTTTTTTTTC[A/T]TATCTTATAATTTTT | 5607 |
rs562927393 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618119 | ACCTTTTATGTATTG[C/T]ACTAGACTCATCTTT | 5607 |
rs562928723 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543230 | TTCCCTTGTTTTCAC[C/T]CTCTGTCCTCTGCCC | 5607 |
rs562949915 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586019 | AATAAAACTGCACTT[G/T]CTCAAGCTCTGACAA | 5607 |
rs562949979 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592275 | AAATTTATTAATTTT[A/T]TTTGTAAAAACACAC | 5607 |
rs562957098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775393 | TTTTGGGGAGGCCAG[A/G]ATACGTTTCAGCTGC | 5607 |
rs562995623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610397 | TGTGCTAGCAGGGGT[A/G]GTCTATTTCTTGATT | 5607 |
rs563000349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543834 | CCAGCCTTGTTTTTC[C/T]ACTGAGTTCTCTGAA | 5607 |
rs563015386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644923 | GGAGGCTGAGGTGAG[C/T]GGATCATTGAGGTCA | 5607 |
rs563016222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661464 | CTTTGTCAAGTCATC[A/G]TTGTGAAACCCAGCC | 5607 |
rs563016456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616397 | TTATTTGTCTTGTCT[C/T]GATCAAACTTTTTCA | 5607 |
rs563019853 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611927 | GATGACCAATATGAA[C/T]AAACAGCTGTCTCCC | 5607 |
rs563026339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574424 | TAAAAATACAAAAAT[C/T]AGCTGGGCATGGTGG | 5607 |
rs563058946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725944 | AGTCTCTCCCTTTTC[C/T]CTCCCCGTACATAGA | 5607 |
rs563074905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668809 | CTTACACAGATGCAG[A/T]AGTTTATAGAAGAAA | 5607 |
rs563079165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679472 | GGTGGACCAAATTTT[C/T]CATGTTTGAATCAGT | 5607 |
rs563096166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577949 | AGGTTGCAGTGGGCC[A/C]AGATTGTGCCACTGT | 5607 |
rs563121978 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687384 | ATTAAAAGAAACATC[A/C]CTATTGTTCAGAAAG | 5607 |
rs563129398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613891 | TTACTCTTTGACCCA[C/T]TAGGGTACTATTTAG | 5607 |
rs563131802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719764 | CAGATAGGAAAACTG[C/T]CCTCAGTGTTGCATT | 5607 |
rs563145200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721913 | CAGTTTGATGCTTTC[A/G]TTACATTTATTATCC | 5607 |
rs563148411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636364 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 5607 |
rs563170545 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718941 | TTAGTTATTTTTAAA[A/T]GTACAGTAAATTTTT | 5607 |
rs563189505 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604319 | AAGAAGAAAAGTTTA[C/G]GAAAAGATAATGAAT | 5607 |
rs563190827 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621161 | TGTGGTTATATTAAC[A/C]TAAGACAAAATAGAC | 5607 |
rs563196423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772004 | ATAGCTAAGTACATG[C/T]TACAGCTACTAATTA | 5607 |
rs563200857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607321 | TCAAATAAAATTAAT[A/T]ATGTATGTTTCCTTC | 5607 |
rs563215400 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671431 | AAAACTGAAGATAAG[A/G]GACTAAAGTATAAAA | 5607 |
rs563225463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567044 | GTTATTTAGAAGTTG[C/T]ATTCTTTTCTTCATT | 5607 |
rs563231519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757732 | GATGGCCTGGGCTCT[C/T]GGAGGACCACAGTGA | 5607 |
rs563234220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660515 | AGTGTACTGAAGATG[A/G]CATCAACATCTTTCC | 5607 |
rs563247160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634283 | CTAAGGTGGGAGGAT[C/T]GCTGAGCTGAGGAAG | 5607 |
rs563260708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785897 | GCTTCAAGTACAGGC[A/G]CTACCTCTAGGAAAC | 5607 |
rs563277271 | in-del | -/AT | 0.0011216 | 0.0236547 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703424 | GTACGTTGTTTGCAC[-/AT]AGACGCTTCTGTGCA | 5607 |
rs563293603 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679366 | ACGATACCAATTTCC[A/G]CAGTCAATTTGGCCA | 5607 |
rs563298958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640995 | TACCTTTTTGTCTGT[G/T]TGTTTGGTGCAGGTA | 5607 |
rs563316704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578584 | ACAACCTAACTACTC[A/G]CTTTAGAGAAACTGT | 5607 |
rs563324074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621916 | TGGCCGGGTGCGGTG[A/G]CTTACGCCTGTAATC | 5607 |
rs563337348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674792 | TAGAAAATGGGCAAA[C/G]ACATGAAGAGACATT | 5607 |
rs563342287 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672983 | TTGTAGATATGCGGT[A/G]TTATTTCTGAGGGCT | 5607 |
rs563353097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710652 | GGGATCACAGGCATG[C/T]GCCACCACGCCCGGC | 5607 |
rs563391955 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791753 | TTGAAAGCCGGTTGT[A/G]GAATGAAAACCACTA | 5607 |
rs563408778 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627678 | AAAAAACTCTTGTCA[A/G]TGATTGTTCAACTCT | 5607 |
rs563417614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67664079 | TTGGAGTACCTTATC[G/T]TCAGAAGATTATAAG | 5607 |
rs563422570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779613 | ATCTCCCAGTTAAGC[A/G]TAGCTTTTTTCCTCC | 5607 |
rs563422869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682444 | TGGCCAGGCTCATTT[C/T]GATCTCCTGATCTCA | 5607 |
rs563424014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568410 | AAAATCATGCAGTTA[C/T]TCAAGTAGAGTTGGA | 5607 |
rs563439373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682690 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGT | 5607 |
rs563451505 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713565 | ACATGGCAAAACCCC[G/T]TCTCTACTAAAAATA | 5607 |
rs563455191 | snp | C/T | 0.000111414 | 0.00746289 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806819 | CCCGTCGCCCTTCTC[C/T]GTATGCTGCCTGCGC | 5607 |
rs563456140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606549 | AGATGCTGGTCTCTC[C/T]TCCTTTCTGTTGCCT | 5607 |
rs563461393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805476 | CGAGGCCATGCGGCT[A/C]TTTAAGCAGCCTCTC | 5607 |
rs563469579 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755151 | AGCTAATTTTTTTGT[G/T]TGTTTTTAGTAGAGA | 5607 |
rs563471389 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719257 | GTAAGAGGGCCTTGT[C/T]GGTTAAGACCATCAG | 5607 |
rs563479462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665146 | CTTGGCCTCCCAGAG[C/T]GCTAGGATTCAGGCG | 5607 |
rs563480801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571703 | AGGCAGGTTTTTTCC[C/T]CATTTTTACAGCAGA | 5607 |
rs563481573 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556040 | ATCTGCCTGTCTCAG[C/T]CTCCCAAAATGCTAG | 5607 |
rs563495491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717442 | TTGCCCTCAGTGACT[C/T]CTTGACTAATAGGTA | 5607 |
rs563531799 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752718 | AGAAATGGAAAGACA[-/T]TTTTGTGTTCATGAA | 5607 |
rs563539744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703555 | CATAAAGTCTTTGAT[A/T]CCTTGTGTGGCTTGT | 5607 |
rs563548371 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750887 | AGTATATACTATTTC[C/T]TGTTAGAGAAAAGTC | 5607 |
rs563576943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702894 | ATTAAAAGAAACCCT[C/G]CTGTTCCAGACCAAT | 5607 |
rs563583607 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642126 | TCCACAAATACAGTA[-/T]TTCCTTACTACATTT | 5607 |
rs563586401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605246 | TTTTAGTAGGGATGG[A/G]GTTTCACCATGTTGG | 5607 |
rs563591069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696462 | CTGACCCTTTACCGA[A/G]AAAGTTTGCCAGCCC | 5607 |
rs563605756 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745727 | CTATGGTCTATGTGG[C/T]ATTCATATAAAGAAA | 5607 |
rs563607618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591738 | AATGCTACTCTACTA[A/G]TCAGGTAGATATTCA | 5607 |
rs563617582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666037 | TTTTATTGATTCTTT[A/T]AAAAATGGACATCTA | 5607 |
rs563630862 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707356 | GATGTAGCAAATCCA[A/G]TTTAAAATCACTATA | 5607 |
rs563634855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765621 | TCTTTGGAGTGTCCA[C/G]CTTACCTGCCTGCTC | 5607 |
rs563652462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696004 | GCTCTTATTGGCCAA[A/G]TGCTCACCTACATGG | 5607 |
rs563669769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663208 | AATCAGGAAACTAGT[A/G]TCGATACAATACTGT | 5607 |
rs563691400 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633709 | ATTCTATAAAATATA[A/G]TAGATACTCACACTG | 5607 |
rs563700913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724398 | TCTTTTTTATTTATT[C/T]ATTTATTTATTTTTT | 5607 |
rs563721285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619017 | AAATGGTGCTACACA[G/T]TCTGTTTTCCTTACC | 5607 |
rs563725345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612964 | GCAGAAGACTTTGTA[C/T]TGCAGTATTGAAGTG | 5607 |
rs563740440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598738 | TGAAGTGGTGGAGGG[G/T]ATATGACTGCAGACT | 5607 |
rs563750930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625997 | AAACGTCCAGGTGTT[G/T]CTTATTCGAAGTAAC | 5607 |
rs563762459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754835 | GCATGCCAAAAAGCG[C/T]AGGTGTTACCCTGTA | 5607 |
rs563784151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789511 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 5607 |
rs563800111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763441 | TTTCTCCTTCTGATA[A/G]CATGTGACTGCTTTT | 5607 |
rs563800797 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779179 | CACAACAGCAAGGGG[A/G]CCCCACGTAGGGTCC | 5607 |
rs563810049 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739379 | GAATTTCATTTACAG[A/T]CAAGCCAGTAAGACA | 5607 |
rs563819684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732419 | GGAAATTTGGCAAGC[A/T]AGATGCCACAGGAAA | 5607 |
rs563824822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647871 | GAGACTCTGTCTTAA[A/C]AAAAATAAAAAAAGG | 5607 |
rs563838747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747201 | AAACTCAGGGTGGTT[A/G]TACAGATCAAATGAG | 5607 |
rs563840120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626288 | AGCAGTTTGGGAGGC[C/T]GAGGCTGGTAGATCA | 5607 |
rs563871125 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591303 | TGAGCTGAGCTCACA[C/T]CACTGCACTCCAGCC | 5607 |
rs563886533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647191 | TGGAGATTCTCAGTA[C/T]ATTACTAAAGCAATT | 5607 |
rs563891370 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632674 | CCTTTTTAGCTATCC[A/G]CAGTGAGAAATTGAT | 5607 |
rs563898027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605658 | CCAGATTTCTATACA[A/G]CATTTCTTTTCTTTT | 5607 |
rs563900314 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547462 | TCTTTTTTCTTTTTT[C/T]TTTTTTTTTTTGAGA | 5607 |
rs563920638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655339 | TGTCTTTTAACTTCA[A/G]TCTAAAGTTCTTTCA | 5607 |
rs563925874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591118 | TTGGGAGGCCAAGGT[A/G]GGCAGATCACGAGGT | 5607 |
rs563943872 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785342 | TCAGTTCAGCTTTTT[A/G]GAGCAAAACGTTGTG | 5607 |
rs563949939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748006 | CCTATTCTAATACAA[C/T]CTGGAGGGTACTAAA | 5607 |
rs563960663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639591 | AGATTTGGCTTGCCA[A/G]GGGTCATCCTGGTCA | 5607 |
rs563961859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640320 | CAAAATATCTCATAG[C/T]GTTCTTTATATGGAC | 5607 |
rs563968702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682318 | GCCTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 5607 |
rs563975726 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802724 | CGGTCACCGTGGGTG[G/T]AAGATGCTCTTGACA | 5607 |
rs564024984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655525 | AATCTTTTTCTTTCA[C/T]GTTCAAATGTCATTC | 5607 |
rs564056134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792099 | TGTGGACAGTATTGC[C/T]TAGAACAGTGGTGGG | 5607 |
rs564068253 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726081 | TTAATGATATCCATC[-/A]AATGAAATGATGATA | 5607 |
rs564076989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578484 | GGAACATAAGCTTCT[C/T]TATTAATACAGACAC | 5607 |
rs564081618 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640149 | TTCCTGCAGATCCTT[G/T]CATATAGGGTATAGT | 5607 |
rs564090270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575957 | TGGAGTCTTGCTGTG[C/T]CGCCCAGGCTGGAGT | 5607 |
rs564092225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567615 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 5607 |
rs564094751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577085 | GGACTACAGGCGCCC[A/G]CCACCGTGCCCGGCT | 5607 |
rs564101702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695866 | AAAACTAAAATTGCT[G/T]TGCTTCTTAGGTGAG | 5607 |
rs564128333 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544898 | TGCATCAAATGCCAT[C/T]CTTCTCTTTGTATCC | 5607 |
rs564139676 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546412 | GCAGGTTGTAGTCAC[C/G]GAGTCAGCCATAACT | 5607 |
rs564146876 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771422 | AGAAAAGTGGATAAG[C/G]CTTCACCTCCCTCCT | 5607 |
rs564165040 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572244 | GTCTGTATGGACAGT[G/T]ACGGGGGAGAGGGTG | 5607 |
rs564175671 | snp | A/G | 0 | 0 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725339 | CCATGACCACTTGCA[A/G]CCGGAAGCTTTGTGT | 5607 |
rs564198470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681255 | GGATGATATCTGATC[G/T]TCCAACACTGGCAAG | 5607 |
rs564200430 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547245 | AGGTTTGTCTTTATC[A/T]CTGTAACCAGTTTAT | 5607 |
rs564210532 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633113 | TGGTGCTCACCGAGC[A/G]CGGCCCAGTCGTACC | 5607 |
rs564211286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633424 | ACATTATACATTTTT[C/T]GTAATTTCATACATT | 5607 |
rs564229780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575215 | GTAGTTGAAACTTTG[A/G]AGTGGCTAAAGTAAC | 5607 |
rs564236758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613201 | GTCTTATTTTCATTG[C/T]AAAGCCATCTTCCAG | 5607 |
rs564263640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664521 | AAAAAAAAAATGTTG[A/C]ATGTATTTAAATATG | 5607 |
rs564285634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779480 | CCACTTAATCTTTTC[A/G]CAAGACTTTAGCAGA | 5607 |
rs564286628 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570824 | TACATATAATAGGGT[A/T]TGCTTGCAGTATTGA | 5607 |
rs564334046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710192 | CATATGCATAGCATA[C/T]GCATTTTGCTCTTTT | 5607 |
rs564374179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709490 | GGGCAAAAAAAAAAA[A/C]AAAACTACAGGGCTA | 5607 |
rs564389975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665071 | AATTTTTTTAAAGAT[A/G]GGGTCTTGCTCTGTT | 5607 |
rs564414827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568906 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATTG | 5607 |
rs564426348 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718855 | ATGTGTAATAATCAC[A/C]TCAGGGTAAATGGGG | 5607 |
rs564465992 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666761 | TGCTATAAAATGCCA[A/C]CTGTTGTGAGAAGAA | 5607 |
rs564485902 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795498 | CCAAATTATTTAGAA[A/G]TATTTTTTATCTCCA | 5607 |
rs564487698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618076 | TAAATTCGCATTAAC[A/G]GTTTAGATGAAGGTG | 5607 |
rs564492142 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793864 | ATTTTCTGAGAGGAC[C/T]AAAGAGTCATGAATG | 5607 |
rs564518748 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658119 | AATGAGCAACGTAGT[-/G]GTTCTCTGCATATAT | 5607 |
rs564523855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805469 | CTCGTGGCGAGGCCA[C/T]GCGGCTCTTTAAGCA | 5607 |
rs564525353 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770573 | CTTCACCAAAGTCCA[C/G]AGTCATGTCCACTGG | 5607 |
rs564543160 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676436 | TAAGAGATTTATCCT[C/T]GGGACATTTTGCCAA | 5607 |
rs564549132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565597 | GTGATTTCTGCACCA[C/T]GTATTCCTTACAGCA | 5607 |
rs564557486 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706478 | GATAACCAGATGGTC[A/G]GGAGTGAGGGCCAGG | 5607 |
rs564621174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746294 | CTGCATGTTCTCCTC[A/G]GAGAATGTTGTCATC | 5607 |
rs564621697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559884 | ATAAGATAGAAAAAG[C/T]TCAAATTATTTTCTT | 5607 |
rs564657738 | snp | A/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547911 | TAGTAGATATTACTG[A/T]TGTTTAAACTTCTTA | 5607 |
rs564673021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545929 | GGTCTTCTGTTTCTT[A/G]AGCATCTCTAAGTTG | 5607 |
rs564687091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762717 | AAAATCTCTATAATC[A/T]CAAACTTCAGTTACC | 5607 |
rs564688469 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572706 | GATATTATTATTATT[A/T]TTTTTTTTTTTGAGA | 5607 |
rs564694321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612192 | AGGAAGTTAGTTTCC[C/T]TCCTCTCACATAGAC | 5607 |
rs564708489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554349 | CAGGTGTGAGCCACC[A/G]CACCTGGCCTTATAG | 5607 |
rs564726845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663014 | AAAAAATTCCCACAG[A/G]TGCTTCACCCATATT | 5607 |
rs564731696 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739733 | TGATCCACCCACCTC[A/G]GCCACCCAAAGTGCT | 5607 |
rs564732464 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746395 | ATTACAAATAACTCC[A/G]TTGTTGAAGCAGATA | 5607 |
rs564734894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717273 | CTAGTTACCTTTCAG[A/G]AACTAAGGCCTAGTT | 5607 |
rs564735154 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706692 | ATTGTAGCCCCTGAC[C/T]TCTAGGGGCTTATTA | 5607 |
rs564766948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647023 | TGAATATTACGGCAA[A/C]ATACAGATTTCTAGG | 5607 |
rs564768453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628689 | CTGTGAATGGCCACA[A/G]CGGTGAAGTTAGGAA | 5607 |
rs564803659 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731251 | CTGCTGACAGCATCA[A/T]TAGCAGCCCCTCTTC | 5607 |
rs564804702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595213 | GGTTCATTGATATAG[A/G]TTATGTGATATAAAT | 5607 |
rs564815364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580469 | AATGCTTTATGTGTC[A/G]TCTAAATATATATCA | 5607 |
rs564838765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562387 | AATATTCTCACATAG[A/T]CTATCTTCAGGTTTT | 5607 |
rs564860428 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720586 | AGTTTGGTAGCAGGA[G/T]AATTAGACGTAAAGG | 5607 |
rs564896813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648752 | ACCATGCCCAGCTAA[A/G]TTTTGTATTTTCAGT | 5607 |
rs564916963 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671683 | TATTATCATTATACT[G/T]TAAGTTTTAGGGTAC | 5607 |
rs564917036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773513 | TTCTTTCACCTTCTT[C/T]AAACAATATGCATTT | 5607 |
rs564923505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727548 | GGTTAGTAACAATTA[A/G]ATGTTCCCATTTTAC | 5607 |
rs564923946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616068 | TTTAGTTTTCCTTTG[C/T]GCCAATGCTATAAAG | 5607 |
rs564924920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608994 | CACAGCCTAAGGATG[A/G]ACACAATGTGTTGTT | 5607 |
rs564928712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550694 | AGTAGCATAAGGGCC[C/G]GGATGCTGAGAGGGA | 5607 |
rs564939109 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767509 | ACTTAGAGAAGCTTC[C/T]TCACTGATCAGAGTC | 5607 |
rs564947643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659419 | CTCAAATTCTTTAAT[C/T]GAACATGGACACTTA | 5607 |
rs564958297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756909 | AGATTCCATTTTGGT[A/G]TGTGTATCGATACCA | 5607 |
rs564966255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802536 | CAGTTTAATTGTTGC[A/G]ATTGGCCCTCAGAGA | 5607 |
rs564968319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714129 | CCCTTTCCTTGTTGA[A/G]CCTACAATGTATTAA | 5607 |
rs564971228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658275 | ATGTATTTAAGTTTA[C/T]ATAAAGTATAGTTTC | 5607 |
rs564988409 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755573 | GGGGAGCCATGTCCA[A/G]GTGAAGAGTCCATGT | 5607 |
rs565006965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796754 | AGTTAGCTTCAATTA[C/T]ATATAATAAAAAACA | 5607 |
rs565012296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793883 | GAGTCATGAATGTGC[C/T]AGGGAAAGTCCTTAG | 5607 |
rs565019545 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752899 | CAAAACAATCATTGA[-/A]AAAAAAAAAAAGAAA | 5607 |
rs565027550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752041 | TGACCGTCTGTCTTC[A/G]GTGTTTTTTGTTTGT | 5607 |
rs565031201 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619164 | CTTCCCCTAGATGTC[C/T]GAATGGTGTGCCCCC | 5607 |
rs565058834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751353 | AATTGTCGCTGGCTA[A/G]CTCAGGTATAAGTGA | 5607 |
rs565067804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558623 | TCTGGCCTCAACCTG[C/T]CCCACCATTGTTTCT | 5607 |
rs565071220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757673 | AGTAAACAGTCATAT[A/G]TGCAGATCACTAAAC | 5607 |
rs565081557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759332 | GGGAGACCAAGGAAG[A/G]CAGATCACTTGAGCT | 5607 |
rs565118779 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725831 | GAATCAGTGTGCACA[-/CT]CTGATTGGCCAGAAA | 5607 |
rs565122029 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601525 | CCTCCAGAGAGCTGG[-/TT]TTCCATGTATACACT | 5607 |
rs565129514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732702 | CCCCGCTGCTGCAGT[A/G]ATTTTCATCTTGTTG | 5607 |
rs565135083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800807 | CCTAAGTGGACGTCT[C/T]TTTTCAAATGACCAG | 5607 |
rs565135818 | in-del | -/CGGACTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576976 | CTCTGTCGCCCAGGC[-/CGGACTG]CGGACTGCAGTGGCG | 5607 |
rs565147430 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746593 | GGTGGTTACAGCTCC[A/G]CCTTCCCTTGTAATG | 5607 |
rs565151329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788189 | TATATATTTGAGTCC[A/C]TGGTTGCAAGCATTA | 5607 |
rs565160121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558167 | ACCAGACTAGTTGTT[C/T]CTTAAGGTCAGTGGA | 5607 |
rs565166493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742960 | TTTTGCTGTACCTCA[A/G]TGCTCCAGCTGTTGT | 5607 |
rs565170999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806606 | AATGAGCGCGGGAGT[A/C]CGAGGACTGCCTGTC | 5607 |
rs565174718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641933 | TCCACCCAGAGTGCC[A/G]AGTCTCCCAGAAAAT | 5607 |
rs565188284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690007 | TGTTAAAACATTATG[A/G]GATTTTTGTGTGTGT | 5607 |
rs565205152 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540626 | ATCACATGCAACTTC[A/G]ATGTTAAATACTAAA | 5607 |
rs565208924 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774373 | TCTAGTACTGCTCAC[G/T]GTTTGATTTTAAATG | 5607 |
rs565230187 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578261 | ACCTGGTGGCCGGTC[A/G]GGACTGCTCTGTGCT | 5607 |
rs565230891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740736 | AAGGCTATCAGAAAT[G/T]TGAATGCATGGCCTG | 5607 |
rs565251283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696591 | CACTCTATAATGTAG[A/G]TAAGACTTGGGTGAA | 5607 |
rs565265943 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541154 | GGATCTGACTAAATG[A/G]ATTTCTACCTAAGCT | 5607 |
rs565267779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748345 | GCCTTGTTTTAAACT[C/T]AGCAAATTGCATTTT | 5607 |
rs565270989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606443 | ATACTGCCTTCATGG[G/T]GTTTTGAAGGTTGAA | 5607 |
rs565277051 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710793 | ACAGGCATGAGCCAC[A/G]GCACCTGGCCATCTT | 5607 |
rs565279416 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67807097 | TGATGGGAATAAAAG[A/T]ATTAATGCTTTGTGA | 5607 |
rs565294624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711366 | TACCAAGGTATCAGA[A/T]CCAGATTTGAATTCC | 5607 |
rs565312238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711728 | AGAAAGGGAAAAGAG[A/G]CAACAGCACTCAAGT | 5607 |
rs565363915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634455 | ATAATGTCAATTAGA[C/T]CAAGTTGGCTGATAG | 5607 |
rs565382641 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718618 | AAAATACAAAAATTA[A/G]CCAGGCGTGGTGGTA | 5607 |
rs565388909 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599125 | TTAAAATTTATCATT[C/G/T]GGTCCAGAATAATGA | 5607 |
rs565396195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772938 | TTACTTTTTAAAAAC[C/G]CACCACCTTTTTGAA | 5607 |
rs565404172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599682 | GCAATTCCCTGGAAA[C/T]TGATTTTTTTTTTTT | 5607 |
rs565406530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549309 | ATGTCAGATTATATA[A/C]CCTTTTTAGATTTTT | 5607 |
rs565417480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555886 | CCTCAGGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 5607 |
rs565442246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635667 | TTTTGGTATTCTTTC[A/G]GCTTTTGTATGTCTA | 5607 |
rs565444398 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638274 | TTCCCTCTATGTGTC[A/C]ATGTGTTCTCATAAG | 5607 |
rs565457365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711943 | TAGTTAATCTTTCAT[C/T]TATTACAAACTAATA | 5607 |
rs565459534 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615277 | TGCTGGAATTATAGG[C/T]GTGAGCCACTGTGCC | 5607 |
rs565466641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690566 | TTGAGACAAGTCTCG[C/T]TCTGATACCCAGGCT | 5607 |
rs565484690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780387 | AGTTCCTTGAAGGAG[A/G]ATCATGATCTTATAA | 5607 |
rs565498470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579717 | AAAAAAACCCTTGCT[C/T]TTGTAATAATTTTAA | 5607 |
rs565501016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806387 | ACCTTCCAGGCTAGT[A/G]CGAGCCTCAGGAAGA | 5607 |
rs565505226 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666511 | GATTCTCACTATAAA[A/C]CACTTCATGATCACT | 5607 |
rs565525004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599986 | TAGAACCTTGAAAAA[C/T]ATGCAAACTTATATA | 5607 |
rs565548176 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, frameshift-variant | MAP2K5 | GRCh38.p7 | 15:67661326 | TCTCATTTCTGAAGC[-/A]GTGACATTGTGTACT | 5607 |
rs565560549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734726 | TTGCACTCTTTGAAA[A/G]GAGGTATTAGAATCT | 5607 |
rs565561896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748485 | TTGCTATATTTTATT[A/G]CATTAATGATTTTTT | 5607 |
rs565564490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726870 | CAAAGTTTTGCCACT[A/G]TTTTCTTTAAATAGG | 5607 |
rs565573537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628215 | GGCTGGGTGCAGTGG[C/T]CCATGCCTGTAATCC | 5607 |
rs565597463 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775542 | ATATACCATTGTGCA[C/G]AGTCTTGTTCTAGAC | 5607 |
rs565629024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634893 | GTGAGAGTATTGAGA[C/G]TATTTACATTTCATA | 5607 |
rs565648563 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613396 | AGGAATGTTTGTTTC[A/T]TTCGGTCAGAGAGAT | 5607 |
rs565654020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613935 | GTAATTTAGTAAATT[A/G]TACCCCAGTGGCCTG | 5607 |
rs565659158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772172 | TAATCTATAGCAACA[C/G]ACTTCTAATTTTGTA | 5607 |
rs565674299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741078 | AGCCTCCTTGAGTCT[C/T]GGCTGTCTGGTGTAT | 5607 |
rs565690587 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799357 | AAGTGCAGGACCTGT[C/G]CTCTGTGTGGAGGAA | 5607 |
rs565691740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664745 | TGACATTTAAGCCAG[C/T]TGATACATCTGGTAC | 5607 |
rs565728121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757236 | TTTTTTGTAATAGCC[A/G]TCCTAACAAAATGTG | 5607 |
rs565737127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546654 | TGGAGACTGAGTTCC[C/T]AGTTTTGGGAAAACT | 5607 |
rs565756093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654835 | GGAGGCCGAGGTGCG[C/T]GGATCACCTGAGGTC | 5607 |
rs565766939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656616 | TTACAGGTGTGAGCC[A/G]TCGTGCCTGGCCACC | 5607 |
rs565776613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798831 | AAAGGAAATGAAGGG[C/T]TGGCAAGGAACCCCC | 5607 |
rs565792917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688430 | CTTAGTAGCATTGTT[A/G]AGGAAGGGGTGCATA | 5607 |
rs565801617 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802518 | AATAACTTCAACCCT[C/T]GTCAGTTTAATTGTT | 5607 |
rs565811453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553776 | AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT | 5607 |
rs565822011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765062 | ACAGTAATATCTCGT[A/T]AGTATAGTACAGTAT | 5607 |
rs565830139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665255 | TAACAGAACACATGA[A/G]AGAATAATCAGATGA | 5607 |
rs565830499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801754 | GCTCAGTAAGTAGAT[A/G]TATACATACAGAATA | 5607 |
rs565836679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733814 | TCTTAATGATATAAC[A/G]ACTGGCACCTTCCAT | 5607 |
rs565849664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696803 | ACCAACATGGAGAAA[A/C]CCCATCTCTACTAAA | 5607 |
rs565850749 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639540 | GTCTTGTTCTAAGTG[C/T]CGGTGACCCCCCTGC | 5607 |
rs565854880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697524 | TTATTTATGCATCTC[C/T]CCCAATCTAGATTAT | 5607 |
rs565856616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695414 | GGTTTTTAAAGAAAG[C/T]TTATACTTTCTTGTA | 5607 |
rs565869395 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540834 | AGGCTATGAAGAGCT[A/G]ACGTGTAATTATATT | 5607 |
rs565873364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546035 | TGCACACTTTTGGCT[A/G]GGTAAGCCCAGGTGG | 5607 |
rs565875197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554611 | CCGGTGATTCCAGAT[A/G]GCATTAATCTCTCTG | 5607 |
rs565890148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648899 | TTTCAGTTCTTTTGG[A/G]TATATACCTAGGAGT | 5607 |
rs565894398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639281 | CTCTAATCCAGATGC[C/T]TGGCTTCTTTCTTGT | 5607 |
rs565895494 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642565 | CAGGTTTTTTCAATC[A/C]GTGCCTGGAGAAGAG | 5607 |
rs565920893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800994 | GTGTATGTTATTTTT[G/T]TAAATCCGTTTTTAA | 5607 |
rs565923087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597781 | TATTTTTTGTAATCA[A/G]TTCTTGGGCTCTGCT | 5607 |
rs565925152 | in-del | -/TGTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625156 | TAAGACCAACTTCTT[-/TGTC]TGGTCATCTATAACC | 5607 |
rs565931305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689256 | TACATACATTACATA[A/C]ATAAATCATATGCTT | 5607 |
rs565933092 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687707 | ATGGAGCTCCTTCTC[A/G]GGCCAAATTCATGCT | 5607 |
rs565939371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683030 | CCTGTAATCTCAGAG[A/G]CTCGGGAGGCTGAGG | 5607 |
rs565955827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556180 | GATTTAAGGGTTTTC[C/T]AATATTAAGGTTGGC | 5607 |
rs565962487 | snp | A/G | 1.77206e-05 | 0.00297657 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646364 | TGCAGGTTTATAACT[A/G]CTTTTGTCTTATTTT | 5607 |
rs565970689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702073 | AGTAGAAGACCCAAA[A/G]TACCTAGCCCAGTGT | 5607 |
rs565983606 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783179 | CATCCTGCCTGACAC[C/T]GAGGAGGCAGCATGT | 5607 |
rs566013504 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735414 | GTTGGTTTGATTCTG[C/T]AGTACCTTCTACACT | 5607 |
rs566065152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590752 | AGACGCTGTGCTTGG[C/G]CCCTTTTGTTTTCTG | 5607 |
rs566070773 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596898 | TGGAATTGGCCGGGC[A/G]TGGTGGCTCACGCCT | 5607 |
rs566074621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715646 | CAGAATTTGAAATTT[A/T]AAAAAAAGCAAAGTC | 5607 |
rs566127471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591217 | AGGCGTGATGGCATG[C/T]ACCTGTAGTCCCAGC | 5607 |
rs566128010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604747 | TAAAAATATAAAAAT[C/T]AGCTGGGCATGGTGG | 5607 |
rs566128582 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602213 | ACGATCTGACTTAGA[-/T]TTTTTCCTGTGTTCT | 5607 |
rs566128846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796302 | TGCTACAAAGAAACA[C/T]CTGAGACTGAGTAAC | 5607 |
rs566160354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639769 | CTTTTAAGTTGAACT[C/T]GTTGCCTTATCTGAA | 5607 |
rs566165539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795539 | GATGTTTTGTTATCT[G/T]GTGGTTATTACCTAA | 5607 |
rs566170091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569346 | ACAACTGATTACACA[A/G]TATATTCTTCAGAGA | 5607 |
rs566184060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685063 | AATGGCTGAAAACTT[A/T]CCAAATTTGGTGAAG | 5607 |
rs566186916 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598325 | TGCTCACTTTTTATA[C/G]ATACTAAGTGACATG | 5607 |
rs566202346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789164 | TGAGTCATTGAGGTC[C/T]TTCCATATAATATAA | 5607 |
rs566207968 | in-del | -/ATAAC | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713069 | TTAAATTTTAATGTT[-/ATAAC]ATGGGAAAAATATAT | 5607 |
rs566237422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732785 | CTAGATTTTGCTGTA[A/G]TGATCGTACTTCCGG | 5607 |
rs566246086 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626425 | CCAGCTCCTTGGGAG[G/T]CTGAGGCAGGAGAAT | 5607 |
rs566246871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620141 | TTTGGGAGGTTGAGG[C/T]GGGTAGATCACCTGA | 5607 |
rs566274319 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542665 | TCCCGGGGTTCCGGC[A/G]CCGCGCGTTTTGGTT | 5607 |
rs566287067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739624 | TAGCTGGGATTGCAG[A/G]CATGTGCCACCACAC | 5607 |
rs566304387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643595 | GGGACTACAGGTGCC[C/T]GCCACCACACCTGGC | 5607 |
rs566333001 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636408 | ATAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 5607 |
rs566347636 | in-del | -/G | 0.00320255 | 0.0398876 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732960 | ATAGCTCTGTGGGGA[-/G]GGGGGGCTTAACAGC | 5607 |
rs566366055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751565 | GGAATAAGTCGGCCC[C/G]TATTGTCTAGATAAC | 5607 |
rs566407369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588445 | TTCCTATGATACTCC[C/T]TTCTTCCTTGTATTG | 5607 |
rs566414471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636266 | ACAAAAAATTAGCTG[G/T]CCGTGGTGTCGGGCG | 5607 |
rs566429129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581826 | GGGTTCAAGAATAAT[A/G]CTGCTCTTCCAGCAT | 5607 |
rs566462234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692712 | TTTTTAATCTCTGAG[C/T]GAGTTTCCTTCATCA | 5607 |
rs566463746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678877 | GCTGAGGCAGGAGAA[G/T]TGCTTGCACCTGAGA | 5607 |
rs566474669 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659755 | TTGAAAAAGAAAAAA[C/G]TATACAACTTCTATA | 5607 |
rs566483054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545127 | CACTCTGCTCTTCAC[C/T]GGTCAATTCCCACCT | 5607 |
rs566486287 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694451 | CTTAGTCTCAGTATT[A/C]TTTCTGTATATATTA | 5607 |
rs566492765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742636 | TGGCAAATGTCTAAA[A/G]TCTTCAAAACTTAGG | 5607 |
rs566495408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628413 | TGAACCCAGGAGGCA[C/G]TGGCTGTGGTGAGCC | 5607 |
rs566533457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782219 | TCAATAATTTTAAGA[A/G]CCCCCAAAACCTGTT | 5607 |
rs566540095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782614 | CCCCCGTGTTTAAAC[A/G]GGCTTGACAGGAATT | 5607 |
rs566557236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628002 | AGAGATCCAAGCACC[A/G]AGTGCTCCTGGGGCT | 5607 |
rs566557840 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623384 | TGTCTCCAAAGTTGG[C/T]TCAACATGAAGTAAT | 5607 |
rs566566854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735796 | AGAAGGTTAAAGTAA[C/T]GAACTTGGACACCAA | 5607 |
rs566591722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579623 | ATTTGTTATTAGTGC[A/G]AACAGCCTTAGATGT | 5607 |
rs566622425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582582 | CTCAGCACTTTGGGA[A/G]GCTGAGGCAGGTGGA | 5607 |
rs566623647 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647738 | AGCCAGGTGTGGTAG[C/T]GCATACCTGTAGTCT | 5607 |
rs566627250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669368 | CAAAGGGTAGGTTGC[A/G]TATTAATCAAAGAAA | 5607 |
rs566630507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773098 | TAAGTTTTTAGTGCA[A/G]TTCTGCAGAAAATTT | 5607 |
rs566634256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623722 | CCTGTCTCAGCCTCC[G/T]GAGTAGCTGGGATTA | 5607 |
rs566635506 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543238 | TTTTCACCCTCTGTC[C/T]TCTGCCCGTCACTCC | 5607 |
rs566649685 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723998 | AGTGCAACTCATAAG[C/T]AAATGAGTTTTTTCC | 5607 |
rs566662117 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696090 | ATGAATCCCTGACTT[C/T]TATCTGCTGACAGTC | 5607 |
rs566682009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566460 | GGATTACAGGCATGA[A/G]CCACCATACCCGGCC | 5607 |
rs566699615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629257 | GGCCTAGCTGCTACA[A/G]AGAAGACATGTTTTA | 5607 |
rs566731522 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647316 | TCAAAAATTAAAAAT[C/G]TTACAGCCATATAGG | 5607 |
rs566733121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657727 | GCCAGTAGCCATATA[C/T]ATATATATATGCATG | 5607 |
rs566736448 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570048 | AACCAAGGTAATAAC[C/T]CTGAAAGTTTCAGCT | 5607 |
rs566740462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768448 | TGTTTGGCTCCCACC[A/G]AATGCTGCATGCTCT | 5607 |
rs566754932 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765466 | TTTACCAGTTTTACA[C/T]GCACTTGTATGGGGG | 5607 |
rs566759574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616690 | TTCTTGTCTTCTACC[G/T]GTTCTCTGAGAGACA | 5607 |
rs566785917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668325 | TTTTCTCTAAAATAA[A/G]CCAAACGTGTGATAA | 5607 |
rs566809164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651086 | AGCTGGGCATGGTGG[A/C]ACATGCCTGTAATCC | 5607 |
rs566823123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676758 | TTAGGTGAAGCAATC[A/G]AGGCTCAAGCAGCCT | 5607 |
rs566828542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727157 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGT | 5607 |
rs566835305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727709 | AAATTAAAATATTTT[A/T]TCAGGGGTGCAACAT | 5607 |
rs566836408 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580022 | CAGAAGCCATCTCCA[A/T]GTTAGGTGGACATAT | 5607 |
rs566855437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781036 | GATGACAGGGGACCC[A/G]AAGGTTTTTATCTGT | 5607 |
rs566859724 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734148 | TTCATTTAAAACCGA[-/T]TAATTTATTTGCTGC | 5607 |
rs566868918 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683635 | GGCTTGTTGGTGGGC[A/G]CCTGTAATCCTAGCT | 5607 |
rs566901497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549969 | TCATATTTCCTGTAG[C/G]ATTTGCCACATGTTA | 5607 |
rs566901557 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565784 | AGATAATTTAAAAAA[A/T]TTTTTTGTAGAGATA | 5607 |
rs566930768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666366 | CTTTTGTATTCCTGT[A/G]TCTAAATTTTTTTAT | 5607 |
rs566940983 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604466 | TTGAGAAAGTAGAGA[A/G]TAGTATGTGTTGTGG | 5607 |
rs566963438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667365 | CTTTTGCTATATAAG[C/T]TCATTGCTGTTCCTT | 5607 |
rs566965710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558306 | TAAGCTTTCTATATC[C/T]CATTCATCAGCAAGT | 5607 |
rs566972642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579177 | TGTGGATCAATAACC[A/G]GCAAATTTCCCATTA | 5607 |
rs566979468 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629956 | CATTTCATTTAAACA[G/T]AAAAGGTACGGTGGC | 5607 |
rs567000155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557323 | TGCATTTTAAGTCCA[C/T]GTAGACAAATGCTGT | 5607 |
rs567007074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557613 | AACCAACACATTATG[A/T]CTCATTTTAAATTTG | 5607 |
rs567037516 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578097 | CTCTGGGTAGAGCCC[A/G]TCTTGATTTTACAAA | 5607 |
rs567044787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698412 | CCATGCTGGTCTCGA[A/T]CTCCTGGCCTCAAGT | 5607 |
rs567072181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673142 | ATTGACTTGGCAATG[C/T]GGTCTCTTTTTTGGT | 5607 |
rs567080719 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602595 | CAGCAGAATTTTTAC[A/G]AGACATAATATTCTA | 5607 |
rs567113462 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597807 | CTGCTTTGTTTTTCC[C/T]ATCCCCCCCAAATTT | 5607 |
rs567142315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706264 | GATTGCCATTGATAT[A/G]TTTGGGTTCTGTTGA | 5607 |
rs567143715 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565234 | TCATCACTGTTATTT[A/T]TTTTTTTTTCTCCGA | 5607 |
rs567145953 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593035 | TACCGTCCAGTTTTT[A/G]TATCCATAAGCTTAT | 5607 |
rs567159329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572851 | CTACAGGCACCTGCT[A/C]CCACGCCCAGCTAAG | 5607 |
rs567160260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550177 | GAAACTGACAAAAAC[A/G]GATTATTTATGACCA | 5607 |
rs567176954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713753 | AAAAAAAAAAAAGTG[G/T]CATGGATCACCCAGC | 5607 |
rs567196434 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759140 | TAAAAAATTCATTCA[C/T]GTAGAATCACTCACT | 5607 |
rs567223613 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609986 | TTAGTAAATCCTTGC[C/T]AAGAAGGTATGTTAC | 5607 |
rs567228683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642305 | ACTTACTAGGCACTA[C/T]TGTGAGTTAGACCCT | 5607 |
rs567239664 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600885 | TCCAAAATTCTGCAA[A/G]ACATCTATTTTCTCA | 5607 |
rs567255603 | in-del | -/TTAATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583479 | TATTTCTGTGTTTTT[-/TTAATA]TGCTATGGTGTAATT | 5607 |
rs567282552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705748 | TCTCAAAAAAAAAAA[C/G]AAAGAAAGCAGACTA | 5607 |
rs567293039 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650919 | TGTTAATTCTTTTTT[A/T]AAAACATTTTAGGGG | 5607 |
rs567311993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786325 | AAGCACATTCCTCCC[C/G]ACTCACTGGAAGCCA | 5607 |
rs567339199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641438 | ATTTTGCTCTCTTTC[C/T]CTTTAGTGAAGTGTG | 5607 |
rs567341704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788428 | TCTCTATTTTATAAA[C/T]ACTCTGCTTCATTAT | 5607 |
rs567343142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634017 | TTTTAAATTTGTTGA[A/G]ACTTATATTATGGCT | 5607 |
rs567350907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642825 | GGTTCTTGATCAAGG[A/G]AATGATATATTCACA | 5607 |
rs567359155 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742406 | AAGCTCCGGAAAAAC[A/C]CTCTCAGACATTTTG | 5607 |
rs567380441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796153 | TAATTGATTAATCAT[C/T]TATATTTATTGTTTG | 5607 |
rs567386410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780478 | TCTCTCTAATCCAAT[C/T]CAGTAAAACACTGTG | 5607 |
rs567387768 | in-del | -/AAA/AAAA/AAAAA | 0.445328 | 0.156035 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592118 | GTGAAACTATGTCTC[-/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAA | 5607 |
rs567395334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549765 | GTAAATACATGACGG[C/T]TTATTTGTATATAGA | 5607 |
rs567398851 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606331 | CAAGATGTTTGAAAA[C/T]TGAATTTTCTATCTC | 5607 |
rs567411946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628883 | GATGGTGGATATGGC[A/G]GCAGTGGGGATGGAT | 5607 |
rs567416122 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610590 | AAAGGCATTTACCGC[A/G/T]TATAACTTTCTGCCA | 5607 |
rs567421726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678017 | TTTCTTATGTGATGG[A/G]GTCATTAGAATAACT | 5607 |
rs567425543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728768 | GCTATTATTATGCAA[A/G]TAAGTGTTGTATTAC | 5607 |
rs567426600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636642 | TTGAGCAGAGCAGCT[A/G]TGCCTTATAATTTTT | 5607 |
rs567444870 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650222 | TTAATAGCTTTTTGT[A/G]GATTCCTTAGGGTTC | 5607 |
rs567454495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684408 | CAACTCTCCTAAAAT[A/G]AAAGGTCTAAAATCA | 5607 |
rs567455453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781389 | TTGAGAGAGACCTTT[C/G]GGGATTGTGAGTCTT | 5607 |
rs567484668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787278 | AAAAGGATGGGAAAC[C/T]GAGTTCAGCGCTTGT | 5607 |
rs567485591 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685011 | GTCTCAAAAGAAGAG[G/T]AAAGAGAAAAGGAAA | 5607 |
rs567488372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636166 | GCCTGTAATCCCAGC[A/T]CTTTGAAAGGCTGAG | 5607 |
rs567503044 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654496 | TCTGCCAATCTCTTA[C/T]TTAATTAGAGTGCTT | 5607 |
rs567506399 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679955 | CCCCAAAAAAGTGTC[C/T]TCATGTTCATTGGCA | 5607 |
rs567513582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598073 | AGCCGGGCATGGTGG[C/T]GTGTGCCTGTAATCC | 5607 |
rs567529050 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675953 | TTCAAGGAACAAATG[C/G]AAATGGAAGAGGATA | 5607 |
rs567529493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774875 | GAGGCCTGCAGGATT[G/T]TCAAGGTTTCCCTGT | 5607 |
rs567561437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629212 | AGGTTACAACAGATT[C/T]GTGAACTCAGCCAAG | 5607 |
rs567588943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677044 | AGGGAATAGTTAGAA[C/T]GTTCCTCACACTTTC | 5607 |
rs567627781 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683592 | CATGGCGAAACCCCA[G/T]CACTACTAAAAGTAC | 5607 |
rs567629899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734439 | TAAATTGTGCTCTGG[A/G]TAGAGTATGTGTTTC | 5607 |
rs567651147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740857 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 5607 |
rs567656763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786779 | ATAGAGTATCGCAAA[A/G]CATGAAATTTAAGTG | 5607 |
rs567658204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592620 | AATTGCCTCTGAAAG[A/G]CTATCTAAAGGCAGT | 5607 |
rs567662353 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642855 | AGCCAGTAGTTTGGG[G/T]TTAATTCCAGGAGGG | 5607 |
rs567680283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793255 | CCACTGTGCTCCAGT[C/T]AGGGCAACACTGTGA | 5607 |
rs567682020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579019 | AGCCTATTGTACATA[A/G]CAGTTAATTAAAGAA | 5607 |
rs567686667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630818 | ATGTTTGGATTTACA[C/T]TTATGTCCTTAACCA | 5607 |
rs567691325 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540704 | TATATTTTGTCATTT[A/G]TGATATCAAGTGGAA | 5607 |
rs567729373 | snp | C/T | 0.000197655 | 0.00993922 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586904 | TCTCAGATTCACTTC[C/T]AAGCAATAGGTGCGA | 5607 |
rs567742510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726259 | AAAGTAGTCACTTTA[C/T]GAGGTCATAATGTTT | 5607 |
rs567745808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627943 | CGATGAGAGCCTGAG[C/G]AGCCATTTTAAGCAA | 5607 |
rs567748861 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708622 | GTGTACCACTGCACC[C/T]GGCTGAACGCCTTCA | 5607 |
rs567749477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638326 | GAACATGTGGTATTC[A/G]GTTTCCTGTTCTTGT | 5607 |
rs567788445 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676806 | ATAGGAAAAGTCATA[C/G]GAAAAAGTCATAGGA | 5607 |
rs567790864 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619165 | TTCCCCTAGATGTCC[A/G]AATGGTGTGCCCCCA | 5607 |
rs567792597 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586889 | ACAGCAGCCCAGCAG[C/T]CTCAGATTCACTTCC | 5607 |
rs567796277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628308 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 5607 |
rs567797430 | in-del | -/CTAA | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661676 | TTTACTTTTTTCTAC[-/CTAA]CTATCAGAATATATT | 5607 |
rs567824636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766609 | CTGGAGCGCAAATTT[A/G]CTGTATGCCTCCCTC | 5607 |
rs567829440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614195 | CATTCAGTAACCTCA[A/C]CAAGCCTTGGTTTCC | 5607 |
rs567857204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579874 | GTTTTTAATATAGAA[A/C]CAGTGAGGATGAAAA | 5607 |
rs567879571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621369 | ACTCAAGAAAATCAA[A/G]AAGGTGGGACAGGGA | 5607 |
rs567890740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770224 | GAGGAGCCACAGGGG[A/C]CCTCAGAGCCTCTAG | 5607 |
rs567892145 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554781 | TTGCTGCCTTAGAGG[A/G]ACACACTTGTTGAAT | 5607 |
rs567902296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719254 | TACGTAAGAGGGCCT[C/T]GTCGGTTAAGACCAT | 5607 |
rs567920776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758380 | TGAGATGGGGCACAC[A/G]GAAAGAGAGGCATTT | 5607 |
rs567921705 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661934 | TTATAAACATTTAAA[G/T]AAATATTTTTGTTAT | 5607 |
rs567924467 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558394 | TTGGTTTAGGCCACC[A/G]TCATCTCTCACCGGG | 5607 |
rs567931954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657639 | GTTTCTTGTTCCAAT[C/T]TGCAAACTACAAGCA | 5607 |
rs567935262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730011 | TTGAATCATGATAGA[A/G]TGTTGTCACCAAATT | 5607 |
rs567973957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737114 | TGAGTCTAAATGGCC[A/G]TCCTTATTTTACACA | 5607 |
rs567988421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790257 | TGTCCTGATGGAGCC[C/T]TGACCAGCAAGCGTG | 5607 |
rs567996792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654100 | ATCTTCTGTATAGTT[A/T]TGTCCATTTTTGAAA | 5607 |
rs568024726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583568 | ACATTTTATCATATG[C/T]AGATAAGTGAAATTA | 5607 |
rs568038177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670801 | AGGGTCAGGGAAGGA[A/C]GGATAGTGGGAAGAG | 5607 |
rs568045502 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589811 | TGTGTGTGTGTGTGT[A/G]TGTGTATAAGAGATA | 5607 |
rs568057300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662640 | GATTTTTTAAGTTTT[C/T]AATGGTGACCACTGA | 5607 |
rs568068534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753885 | TAGAAAACATATGTC[C/T]GCATAAAAACTTATA | 5607 |
rs568069281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721978 | AAGTTAATAATAATA[A/C]AACAAACTAATTGTC | 5607 |
rs568083999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616651 | AACTTTTATTTATTT[G/T]AAAATAGCCTTTGTT | 5607 |
rs568092000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756666 | TAAAAGTAAGTTTGT[A/C]CCCTTTGACGAACAC | 5607 |
rs568125172 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730814 | CTAGTGGCAAATTGA[A/G]AGGAGTGGCCTATTG | 5607 |
rs568125663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782192 | GAGGCAGTGTCTCCC[A/G]CCTCTGCGGTTTCAA | 5607 |
rs568137772 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626181 | CAAAGTCTTACGTAT[-/TA]TGTTACTTGGATTTA | 5607 |
rs568145604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723152 | TATGATTCTATGACA[A/G]TAATTATTTTTATTA | 5607 |
rs568156675 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785923 | GAAACTGGGCAGGCA[A/G]CAGCTGTTTACTTAG | 5607 |
rs568166553 | in-del | -/C | 0.00240144 | 0.0345681 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560905 | TTTATGTAATCGGTG[-/C]CCCCCCCTTTTTTTA | 5607 |
rs568214834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67716901 | AAATCAGCAACTTGA[A/G]GCACCAAATATTGTT | 5607 |
rs568225492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609423 | TATTCTATAGACCTA[C/T]TCTATAGGTCTATAG | 5607 |
rs568233504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715361 | TCCAGCTGTCTCATA[A/T]TACCATGCCTAAATG | 5607 |
rs568237220 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779981 | CTCAGCCTAAAAGAG[C/T]CTCCTCTCCCCTCCC | 5607 |
rs568278784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625415 | AAAAATGCTTCCTCC[A/G]TGCAGTCATTGAATC | 5607 |
rs568281539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709837 | TAGCCTTGCAATTTG[C/T]AGTATTTAGGATGAT | 5607 |
rs568283268 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804830 | TGCACGCTTGGACTT[C/G/T]GGGAAGGATTTCCTC | 5607 |
rs568285096 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768910 | ATGTGGTGGTGGTTG[C/T]TTGTTGCTGTGTAGT | 5607 |
rs568296920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762978 | CAAAATGCCCACACA[A/T]GTAATTTGTCACGCC | 5607 |
rs568302539 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723753 | TTTCAGTACACTTTT[A/T]AAAAAAAAAAACTAG | 5607 |
rs568304359 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716260 | GCAGGAGGATCCCTT[A/G]AGCCCAGGAGTTTGA | 5607 |
rs568319781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566395 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGATCTCA | 5607 |
rs568338977 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752408 | AGACAGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 5607 |
rs568348500 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601524 | TCCTCCAGAGAGCTG[A/G]TTTTCCATGTATACA | 5607 |
rs568363000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609753 | TAGAAGAGGTGCTCA[G/T]GAAGACCTATCTGAG | 5607 |
rs568396469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623675 | TGATCTCGGCTCATC[A/G]TAACCTCCACCTCCT | 5607 |
rs568407734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637584 | CTGGCCTCAGGTGAT[C/T]TCCTGACATCTATGT | 5607 |
rs568412328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794216 | CAGGCTTCTGTACAT[A/T]TAATTTTCTTCAACA | 5607 |
rs568420829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767824 | CGTTTTTCATGTCGT[C/T]TCTGTGTAATGCCTG | 5607 |
rs568429071 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570770 | GGACTGCAAATAGTT[C/G]GTTAGTTTATTGATT | 5607 |
rs568452482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744105 | CATCTCTGGGGTTCC[A/T]TCCTTTCATAAATAC | 5607 |
rs568472210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668190 | TAAGAATGTGGCATG[C/T]TTTTATTATAACCAT | 5607 |
rs568475061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637475 | CCTTGCAAATTGCAA[A/G]GTTTTTCCACACTGA | 5607 |
rs568483349 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559077 | ATTAACTCCGTGCCT[C/G]AGAAGGGCTTTAAAC | 5607 |
rs568492057 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620473 | ACACGAACATATAAG[A/G]CAATAGAGTAGTTGA | 5607 |
rs568499578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768374 | CATCAAAGCTATTTC[C/T]TCTCGTTCTCAATAA | 5607 |
rs568508515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789317 | TGACTGTGTCTCTAT[A/G]TATACATCTTTGTAT | 5607 |
rs568514940 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599068 | GCAACTCTGCTAGTT[C/T]AGCATCTCGTCACTT | 5607 |
rs568526858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644251 | ATAGAAAAATCAACC[A/G]GGTGTGGTGGCAGGT | 5607 |
rs568547912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617137 | AAGGGGTATTTCCGT[G/T]CTCATTTTGATAACT | 5607 |
rs568553386 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643948 | CTTCAGTTGTAATAC[A/T]AAATGTAATTCAAAG | 5607 |
rs568557049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623515 | TAGTCTAACTAGCAC[A/G]TAGAGACACTACTGC | 5607 |
rs568565397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679170 | GGGCTGGGCAGTGGG[A/C]GGAGGAGCCCTTTTG | 5607 |
rs568589103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707904 | TTTTTTGTGTGCATG[A/C]CTTCTTCAAAGTATT | 5607 |
rs568621744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782695 | ATTTTTAAATTAAAC[A/G]TGACTTTTTTTTTAA | 5607 |
rs568670774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771469 | AGCTGTTATTTAAAA[C/G]TTTTATGGAGACAGA | 5607 |
rs568677672 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639148 | CTAATTAAACTAAAG[A/G]GCTGCACAGCAAAGG | 5607 |
rs568681973 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692196 | AGGGATAGGATGATG[A/G]GTGTATTTACTGTTG | 5607 |
rs568682592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596242 | CCTGGCCAACATGGT[A/G]AAACCTCTTCTCTAC | 5607 |
rs568682933 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799717 | AGGCCAGACAGATCT[C/G]CCCAGTGGGCCCACC | 5607 |
rs568685758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624167 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 5607 |
rs568697995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596965 | TCACGAGGTCAGGAG[A/C]TCAAGACCATCCTGG | 5607 |
rs568702790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669473 | AGTTAGAGTAGACAC[A/C]ACAGGATGTGCCCGG | 5607 |
rs568716889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689919 | GGGCAAACTTGTCCA[A/G]CCCATGCTCCACGGG | 5607 |
rs568730015 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693964 | GCTTTGTCACCAGAT[C/G]AAAATTAAATTACTG | 5607 |
rs568730796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645308 | CATAGTGAAACCCCC[A/G]TCTCTACCAAAAATG | 5607 |
rs568732008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589371 | TTTCTTTTGCCTTAG[A/G]TGAATAACTGTTTAT | 5607 |
rs568740195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701179 | ACAGGGGTTAGGGCA[C/G]CATTTAGTTATTTCT | 5607 |
rs568764906 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688575 | GCCACAGTAGCAATA[G/T]AAATTATTTTCTAAA | 5607 |
rs568790941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693281 | ATCCTGCTTAAGTGA[A/C]TTGTTTAAGGTTATC | 5607 |
rs568809580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551883 | TTTTTTACATTTGTA[C/T]GGAAAGATATCTGTG | 5607 |
rs568838154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670663 | TGGTTCCTGACAAAT[A/C]CTACCTAGGTTTGAT | 5607 |
rs568857078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636889 | TGGGCTGGGAGAGGC[A/G]GACCCACCTGCAATC | 5607 |
rs568864032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588722 | ATTATTTCTAGTCCC[C/T]TCATCCTTTTCTCTT | 5607 |
rs568865992 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630463 | AGCAAAAAAAATGGG[-/A]AAAAAAAAGCAAAAT | 5607 |
rs568867231 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766005 | CAAACTTTTTCCTAT[C/T]GTCCTTCACTGTTCT | 5607 |
rs568884477 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623012 | GAGGCTGAGGTGGGA[A/G]TATGGCGTGAACCCG | 5607 |
rs568887280 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662772 | GGCTATGAGAGTGAA[A/G]AATGCAAATCTAATT | 5607 |
rs568913565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737034 | GTCTCCCACTCACAG[C/T]GCAGTGGTCTTTTTA | 5607 |
rs568946143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776228 | CACCTCCACTTCTGC[C/T]TCCAATTCTTTTCCT | 5607 |
rs568953111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729585 | ACCATCCTGGCTAAC[A/G]TGGTGAAACCCCGTC | 5607 |
rs568964474 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544122 | CCAGGCTGGTCTTGA[A/C]CTCCTGCGATTTGCT | 5607 |
rs568967445 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803800 | TAGGCAGGCCTGAGT[C/T]GCCAAGGTAGAAACA | 5607 |
rs568984455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715614 | ACATACTCATATCAT[A/G]TATACACACAAATAC | 5607 |
rs568992761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575346 | GAGTGGTTGGAGAAG[G/T]AGGAAAACCCATGGA | 5607 |
rs569012567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623576 | TGAAATCACTCAGCC[A/G]GTTTGAAAACTTACT | 5607 |
rs569024195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661762 | TTTTAGTGGTGAGCT[A/G]TCTTTAATGGATAGT | 5607 |
rs569050608 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731366 | AGCAACATAAAGGTT[A/T]AAGGGCTGGGTTTTT | 5607 |
rs569070562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630559 | TCTGGAGCCAAAAGA[C/G]CTAGGTTTGAGGTCT | 5607 |
rs569076960 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769977 | ACAATTTTATAGCCC[C/T]TACTGAACGGACGTA | 5607 |
rs569103830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769533 | ATCCTTCACATGGGT[G/T]GGTGGGGAATATAAA | 5607 |
rs569107631 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573458 | CTCGTGAGAATCCAC[A/T]CACTATCATGAGAAC | 5607 |
rs569111056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722375 | TTTTTTTGGTCCTGC[A/G]TTACTAAATCCTCCA | 5607 |
rs569112599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651166 | GAGGTTGCAGTGAGC[A/C]AAGATCATGCCACTG | 5607 |
rs569114946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729916 | GTCAAGTGGAAGTTG[A/G]AAAATTCTAATACTA | 5607 |
rs569130575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759791 | CTGCAGACCCACAGT[G/T]TCTGACTATAGTGAT | 5607 |
rs569135257 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546052 | GTAAGCCCAGGTGGA[A/G]CATGTTTTGTCAGAA | 5607 |
rs569147410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616577 | GAAAACAAAGAACTG[A/G]TGTTATTATTTGAGA | 5607 |
rs569150754 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704845 | TTATCATTTATTTTA[A/T]AAATGACTGGATATA | 5607 |
rs569212141 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767749 | TATTGAGGACTTGTC[A/C/T]TGCTATTTTGTGTCT | 5607 |
rs569222275 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773955 | AACAAAGGAATAGGG[G/T]TTCATAAAACAGATA | 5607 |
rs569262707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676855 | TGGAAAAGCTCTAGT[A/G]TGAGGGTCAGACCCA | 5607 |
rs569278462 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740333 | GAACAGAAATCCTGA[A/G]GCTCTAAATCAATTG | 5607 |
rs569284883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620111 | GTGCAGCGGCTAACG[C/T]CTGTAATCCCGCACT | 5607 |
rs569291426 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744851 | AATGATGGTCCTTGT[A/G]AGGAAATATATGATA | 5607 |
rs569293292 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775211 | TTAATGTAAAACTCA[A/G]TGTTAGACTTTGGAG | 5607 |
rs569352903 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756776 | TACATATTAAGTGAG[A/G]TCATGCAGTTTTTGT | 5607 |
rs569358075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550958 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTTGCCAT | 5607 |
rs569365235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667565 | AATACTAATGAGTGA[C/T]CTATACCTCTTCCTC | 5607 |
rs569370751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572526 | AAGAATAGCTACTCA[C/G]TCCATAGAGTAGGAC | 5607 |
rs569381669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766727 | CTTTAAAAAGAGAAA[A/G]GTGTACTGTCAAGTC | 5607 |
rs569399404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714546 | TGAACTGGTCCGAGG[C/G]GTGACGGATGGCTCT | 5607 |
rs569416630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601808 | TTTGATTTCTCAGGC[C/T]TAGAAGCTCTTTTGA | 5607 |
rs569419692 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607776 | TTATTGTTTTATTGC[C/T]TGGAAAAGGGTATCT | 5607 |
rs569424194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612719 | CCTCTCTCCAGCCTG[A/C]CAAAAGCCATTTCTT | 5607 |
rs569435596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707046 | TCAGCCTCCCGAGTA[G/T]CTGGGACTACAAGCG | 5607 |
rs569466618 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602507 | CTTTAGTTTTATATT[A/T]ATTGAAGGTCTATTG | 5607 |
rs569488692 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651645 | GTGTCCAGATTATTT[A/C]ATTTAAAATAATATC | 5607 |
rs569495591 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792389 | CCTCTCAGGGGTTAA[A/G]TCTGTCTTTGGGGCT | 5607 |
rs569497757 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706450 | ACTGTGTTGGCTCGT[A/G]TGGTAGAGAGCAGAT | 5607 |
rs569499419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558968 | GCAAAGAAGTAAGGA[A/C]GGAATCAGGAAGAGG | 5607 |
rs569501395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717852 | GTGATTGCAAAAGCT[A/G]CAGATCTGTTAAGGC | 5607 |
rs569511050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652439 | AGGAAGCTTCCATTC[A/G]TGGAGCAAGAGAGAG | 5607 |
rs569512153 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548296 | AGTTGTTTTCCCCTC[A/G]TTTTTTTAAACCTAC | 5607 |
rs569515136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558334 | AGTCCTGTTGGCTCT[A/G]TCTTCAAATTTATCC | 5607 |
rs569525339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743533 | TGTAGTTAGCCAGAG[C/T]AAATTTTGTTCTCTT | 5607 |
rs569526563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595524 | TAATGATTTATAAGC[A/G]ATAGGTACTGATTCT | 5607 |
rs569537818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771074 | TGTTAGAACCATTAC[C/T]CAGAAATGTATATCC | 5607 |
rs569552926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683155 | CTCAAAAAAAAAAAG[C/T]TGTAGAACTTGCATG | 5607 |
rs569557103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566335 | GCCCGCCACCACGCA[C/T]GGCTAATTTTTGTAC | 5607 |
rs569568945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570310 | CATCTGTCCAATAAC[A/T]TGAGCCTATAAATAG | 5607 |
rs569592719 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569267 | GAACTTAACTTTGCA[G/T]GTGGCAAAATCAGTT | 5607 |
rs569594369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640802 | GGTAGGAATATATTA[C/T]AAGATATTTTTAAAA | 5607 |
rs569596667 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574445 | GGCATGGTGGTGGGC[A/G]CCTGTAGTATCAGCT | 5607 |
rs569611731 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799259 | AACTCTGCATTCGTG[A/G]CATTTGCCCAGGTAT | 5607 |
rs569614796 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588629 | AATGCATGAATGTAT[A/G]TATGAATTACTTGTA | 5607 |
rs569622020 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586600 | TTGGATTTTCACACT[A/G]TTTATGTCTCCTTTT | 5607 |
rs569639881 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747727 | CCACTCCTAAGTTAG[C/G]TGCAAATACTTCAAC | 5607 |
rs569641719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757057 | CCTTTAGATATACAC[C/T]GAGAAGTTGGATTAC | 5607 |
rs569653944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779088 | CTCATTAGCTATGCC[A/G]CCCAGAATTTGCAGT | 5607 |
rs569654041 | in-del | -/T/TTTT | 0.000400805 | 0.0141507 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630868 | TCCCAAATGATTTTG[-/T/TTTT]TTTTTTTTTCTTCCC | 5607 |
rs569682008 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801760 | TAAGTAGATGTATAC[A/G]TACAGAATATAGAAG | 5607 |
rs569690807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562908 | AGGAAGAATGGAGAA[A/C]TCGGGGTATGGTGCT | 5607 |
rs569691518 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737228 | AATTGCTGACTGGCT[A/G]TGGATCCCTGGGGGG | 5607 |
rs569694596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763799 | CAGGCAACACGCTAT[C/G]CTGCTGGGCATGAAG | 5607 |
rs569726673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577224 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCAGTAA | 5607 |
rs569735170 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802820 | GCCTGATGGGGCTGC[A/G]AGAGCTTGCCTGCAT | 5607 |
rs569745098 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718512 | CTCATGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 5607 |
rs569745985 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586194 | ATAATCCTAGGTGCT[-/G]GTATCTACAAAGATT | 5607 |
rs569752912 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767801 | TTGATCAGCCACCCA[C/T]CCACCTCCGTTTTTC | 5607 |
rs569776610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694827 | ATGTTTATTGTGGCA[C/T]TATTCACAATAGCAA | 5607 |
rs569794808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663813 | CCAGGAATTTGAGGT[C/T]ACAGTGTGCTATGAT | 5607 |
rs569794978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605446 | ATTATACACATTATA[C/G]TTCTGTATTTTCTTC | 5607 |
rs569809603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599891 | TATAGGGAGCTCTCT[A/G]AACTCTAAAACATTA | 5607 |
rs569811255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689509 | TCTTTTGAGACAGTG[A/G]TTAAAACAGTCTTGT | 5607 |
rs569829824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648825 | ACCTCGTGATCTCCC[C/T]GCCTTGGCCTCCCGA | 5607 |
rs569836852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655662 | TGTCTTTGGCTATGG[A/G]TAGTTTGATAATAAT | 5607 |
rs569849500 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675531 | TGACTATCAGTGTCA[A/G]TACCCTGGTTGTGAT | 5607 |
rs569907469 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806314 | GCCGTGCGAGTGATG[C/G]CGGGCAGAGGAAGGG | 5607 |
rs569911901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714928 | AAAGTATACACTCAA[C/T]GTGGATCATGTTCAG | 5607 |
rs569924365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707205 | CAGGCGTGAGCCACC[A/G]TGACCAGCTGGTTCT | 5607 |
rs569925220 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591970 | TACAAAATTAGCCAG[G/T]CATGGTGGCACATGC | 5607 |
rs569927522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696670 | AGACTTAAGTTGTAC[A/C]AAACATACATTTAGA | 5607 |
rs569949933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563522 | AAGGGCATTATTTTC[A/G]AAAGACACTTACTGA | 5607 |
rs569951757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554847 | AATTATAAAATGTAT[A/G]TGGTCTAAATCTAAA | 5607 |
rs569955747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653551 | TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTGGG | 5607 |
rs569966430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704807 | TTGCTGTTATACAAT[C/T]TCCTTTTGCATATTT | 5607 |
rs570042184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745777 | ATTGAGAAAATGAAT[C/T]AATTACAATGATGTT | 5607 |
rs570057922 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619797 | TTAGCCAGCCATGGC[A/G]GTACTCTCCTGTAGT | 5607 |
rs570068978 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798691 | ATGGCTAGAGGTAAG[A/C/T]AATTTGCTGCTAATA | 5607 |
rs570071106 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597115 | CGGAGCTTGCAGTGA[C/G]CCGAGATCACGTCAC | 5607 |
rs570080077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753567 | TGAAGAAGATAAACA[A/G]ATGGTCAATAAGCAC | 5607 |
rs570108975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632008 | CAATCTGTTACTTCC[C/T]GTCATGCCCTTTATC | 5607 |
rs570140757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624879 | CAGGTGATCCACCTG[C/G]CTTGGCCTCCCAAAG | 5607 |
rs570160298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745154 | CATTGTCCCAAAGTA[C/G]TAGTTAGACATAGAA | 5607 |
rs570164535 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684033 | AGACAGAATTTGGAG[G/T]TCAAGGAGACCAAAA | 5607 |
rs570169725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770879 | AAATTTTTCTCCCCA[A/T]TTAAAAAAATTTTAT | 5607 |
rs570169876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762544 | CATTTCTAAGTAAAT[A/T]TAAGTCTTTTAAATG | 5607 |
rs570192276 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623680 | TCGGCTCATCGTAAC[C/T]TCCACCTCCTGGGTT | 5607 |
rs570199384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738500 | AAGTCACTGACAGTA[C/T]ATGATTTCTACCCAA | 5607 |
rs570204771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645571 | TAGTTCTTTTTTTTA[A/G]GAGACAGGATTTCTC | 5607 |
rs570216949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639695 | GAATTCAAGATCCTC[C/T]ACGACATGTCGTCAG | 5607 |
rs570248818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625677 | CTCGACTCATGCCTG[G/T]CATTGCCTTTGTCAT | 5607 |
rs570257399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770318 | CCTTCTGCCTTTTTC[C/T]TCCTAGCAGAACGCA | 5607 |
rs570259361 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540700 | AAGTTATATTTTGTC[A/G]TTTATGATATCAAGT | 5607 |
rs570281278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681336 | CTCAACACTGAGCAT[G/T]TGAGTGTTGTGAGTA | 5607 |
rs570336703 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777572 | ATTAAAAACATATAC[C/G]CATTCTATCTGTATG | 5607 |
rs570338226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778445 | AAATCTTCTGATCAC[C/T]GTGAAAGACAAAATG | 5607 |
rs570343192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688308 | AAAGGCTTTGGAGGT[G/T]TTAGGCAAAGAAGTG | 5607 |
rs570352929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620057 | CCTGAGTGATAGAGT[A/G]AGACCCTGTTGCTTA | 5607 |
rs570372898 | in-del | -/TAAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560809 | CAAAATATTTTGGTT[-/TAAG]TAGCCTTAAAGGTTC | 5607 |
rs570422980 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550834 | TGGAGGGCAGTGGTG[C/T]GATCTTAGCTCACTG | 5607 |
rs570424631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576437 | CTTGTTATCCCCTTG[C/T]TGAATCTGGCCCTCT | 5607 |
rs570441107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67716996 | GGACTTTTCTAGAAA[A/G]GTTAAGTGAATAGCT | 5607 |
rs570454554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680381 | TTTGTAAATCATAGT[G/T]TATCAGGCCATCTAG | 5607 |
rs570470125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716070 | CCTAGTATGTGGCAG[A/G]CCCTGTGCTAGTCAC | 5607 |
rs570471952 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707992 | AAAATGTAGGAAACC[A/G]AGCAAAGGAATTTCC | 5607 |
rs570481872 | in-del | -/A | 0.0777841 | 0.181223 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739280 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5607 |
rs570483708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671937 | TTGTCCTCATGATAG[C/T]TTACTGAGAATGATG | 5607 |
rs570493332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673111 | GATTCCTCCAGCTTT[C/G]TTCTTTTGGCTTAGG | 5607 |
rs570525436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584141 | TAAGTCCTCTACATT[A/G]TTAAAAGATATGTTA | 5607 |
rs570532416 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756342 | TACACATAAGTTTTG[A/G]ATACAGTTGTGCCTT | 5607 |
rs570534099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604820 | GAATAGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 5607 |
rs570540351 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785134 | ATTTTCAGTAGAGAC[A/G]GGGTTTCCCCATGTT | 5607 |
rs570559144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575460 | GATGTCTTCACACTG[C/T]TTCGCCAGCCTCTGA | 5607 |
rs570561638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603957 | TAATAAAGCTAATAA[A/G]TGCAAAGCAAAAGTT | 5607 |
rs570563591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596318 | ACTTAGGTGGCTGAG[A/G]CATAAGAATAGCTTG | 5607 |
rs570621032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565272 | TCTTGCTCTGTCACC[A/G]AGGCTGGAGTGCAGT | 5607 |
rs570625529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603331 | CATTCTTCTATATGT[A/C]CTTGCCACAAGTTTT | 5607 |
rs570629049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663621 | CTCCCACCTGTAGTC[C/T]CAGGGATTTGGGAGG | 5607 |
rs570641828 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754233 | TTACTTTAAAAGGGT[A/G]AATTTTATTTTTTGT | 5607 |
rs570648361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746555 | GTTTGGCTTGTTACT[A/G]AAATTCTTAACCACT | 5607 |
rs570675402 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717774 | AGTGGCTGGGACCCT[C/T]CTCTCCCATCTCCCC | 5607 |
rs570680963 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620843 | GTGAATAGAATGTGT[A/G]ACTTCAAAACAAATA | 5607 |
rs570681865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756073 | TAGGGCACAAAGGCC[C/T]TTTTCCTAGAGCTGT | 5607 |
rs570702631 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553820 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 5607 |
rs570705081 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599928 | GGGCACCTACTATTC[A/G]TAATACAAATGAGAG | 5607 |
rs570706358 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709945 | CTGGTTTGGGATTCT[A/C]TGTGGTGGGTTATTA | 5607 |
rs570708851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559928 | ACTACTTTCTAGTGT[C/T]GTTCTCTAACATATT | 5607 |
rs570714360 | in-del | -/G | 0.00159681 | 0.0282109 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626825 | GGATCGCTTGAGCCC[-/G]GGAGTTCAAGGTCAC | 5607 |
rs570728850 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596285 | AAATTTGCTGGGTGT[A/G]GCGGCCCATGCCCAG | 5607 |
rs570735505 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576611 | AGCTGATTGATCTTT[C/T]ACCCAGTTAGCTTAT | 5607 |
rs570740457 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625966 | TAATCATTTTCTTAT[C/T]GCTGCTGCTGGTCTC | 5607 |
rs570744983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569190 | TAAAGAACAAAGAGG[G/T]TAGAAGCTCATTTTC | 5607 |
rs570767972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660611 | TCAGAAACAGAGAGT[A/T]GGGAAATAGGTGTAT | 5607 |
rs570800951 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791283 | AGGCAAAGACTGAAG[G/T]ATCAAAGGGCTTCAA | 5607 |
rs570803842 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546562 | GGACTGGCTGAACTA[C/T]GGAGGCTGACCTGAC | 5607 |
rs570839170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769374 | CTTTTTTCACCTCCC[C/G]CTCTCTCAGCTCTCA | 5607 |
rs570840946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760854 | CCATGATGGGACCTA[C/T]ACACCCTGAGCCCAA | 5607 |
rs570867935 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807411 | ACACATCCACCTGAC[C/G]TGCGTGGCTGAGGAG | 5607 |
rs570871826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705147 | GTGATAAAATGACAT[A/C]AAATGCAGAGGCATG | 5607 |
rs570881226 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788876 | TCTCAGGATGCTGAG[A/G]TGAGAGGATCACTTG | 5607 |
rs570911587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644350 | AGTGAGCCAAGATCG[C/T]GCCACTACACTCCAG | 5607 |
rs570925436 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673857 | TTTTTGTTTGTTTGT[A/T]TATTTTTTTGAAACA | 5607 |
rs570935864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694082 | TTGTTATTCATGCCT[A/G]TTGTAAGATTATTTA | 5607 |
rs570938045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610569 | AATAATTCACTGGAA[A/T]GTCCAAAAGGCATTT | 5607 |
rs570942873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653390 | TCCTGGGTTCAAGCC[A/G]TTCTCCTGCCTCAGC | 5607 |
rs570965778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592764 | TTTGATACCTTTTGC[A/G]TTTGGCCAGTTACTT | 5607 |
rs570973082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661676 | TTTACTTTTTTCTAC[C/T]TAACTATCAGAATAT | 5607 |
rs570976510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745064 | CCAGAAAAGGGAAGA[C/G]GTTCATCTATCAAAA | 5607 |
rs570976541 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659145 | ATTCTTGTATTTTCT[A/G]TATGCACTAATATAC | 5607 |
rs571000165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761462 | CAAATAAAGCCAACA[C/T]TCATACACGCAGCCA | 5607 |
rs571015612 | in-del | -/GAAA | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758381 | GAGATGGGGCACACG[-/GAAA]GAGAGGCATTTTCAA | 5607 |
rs571025174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600136 | TAATATGATTTCTGC[C/T]TAATTATTGCTGTAT | 5607 |
rs571025788 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768646 | AGGAAAAAAGCCGCC[G/T]AAAGGTATTTTTAAT | 5607 |
rs571029238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782901 | CTCCTTCCTGCCTTC[A/G]GAAACGGCCCCCTTT | 5607 |
rs571032282 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740152 | GAACCTTTAATAAGT[C/T]ACTCATTTCTGTGGG | 5607 |
rs571045275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631064 | GGGGAAGCTGTGGCT[C/G]TCTGGTGACATTCAG | 5607 |
rs571055032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798663 | CCCCTTAGGTGCCTG[C/T]GTACTGTCTAGGATG | 5607 |
rs571056518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790366 | ACTTCTGAGTGTGAG[G/T]TCTTTCCACAGAGCG | 5607 |
rs571089522 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693421 | TAATTTTTAGTTGAT[G/T]TATATGAATGATGAT | 5607 |
rs571093171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798167 | ATGCTGCAGACTCCA[C/T]CTTTCAGGGGTGAGT | 5607 |
rs571101295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593369 | CTGAAACTAACACTG[C/G]CTTTTTAGGGAGGCA | 5607 |
rs571116358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801157 | GAAGTGTTATCACAG[C/T]CAAGCGGGCTGGAAT | 5607 |
rs571116542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713007 | ATAGAAGTTCCAGGA[A/G]GAAAGAACAGAGGAA | 5607 |
rs571119240 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698083 | GATACCTTCATCCAA[A/G]CCATGAAAGATTTTC | 5607 |
rs571123459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639076 | GAGTGGGATAAAGAT[G/T]TCATGATGAAGACAC | 5607 |
rs571141683 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694810 | AAGACACATGCACAC[A/G]TATGTTTATTGTGGC | 5607 |
rs571156680 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655508 | TAGAATTTTTGGTTT[A/T]TAATCTTTTTCTTTC | 5607 |
rs571166439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557234 | CCAGCATTTTCTCTA[A/G]AGAAGTAACTGCTAT | 5607 |
rs571172163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790852 | TTTAGGCCACTGATA[A/G]TTATGACTATGGAAC | 5607 |
rs571176563 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686771 | TTTAAACTTTTACAC[A/G]GCAAACTTTTTGGAT | 5607 |
rs571185841 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727298 | TCAAAATTAAGTGAC[G/T]GGCTCAGAAACAGAG | 5607 |
rs571203681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545007 | ACATCTGGATTGGCC[A/C]CTGTCTGCCTGGCAC | 5607 |
rs571213810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636501 | ATATCTGGATCAGTT[G/T]TGACTGATTCCTCTT | 5607 |
rs571236785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594156 | ATACAGCTAAGGAGA[A/G]TCTAGTGTGGTGTAT | 5607 |
rs571255687 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696934 | CGGTGAGCTGAGATC[A/G/T]CACCATTGCACTCCA | 5607 |
rs571280549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757346 | CATTGATTCAATAGT[G/T]GATGTTCACACATTT | 5607 |
rs571283526 | snp | A/G | 1.65201e-05 | 0.00287398 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748633 | TGTGCTTTCACTCCT[A/G]AAGTCATTCCTAATG | 5607 |
rs571306756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792459 | AGAAGTGACAAGTTC[A/G]TTTAAAAAGCCTGGT | 5607 |
rs571312859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749801 | ATTATCTTAGATTCC[A/G]AAAGCCTACTATCCC | 5607 |
rs571334209 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713376 | GAAAATGAATTGTGA[A/T]CTTCTATACGTATAA | 5607 |
rs571340916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801845 | ACACCAGCAAGTTAT[G/T]AAATTATTCAAATGC | 5607 |
rs571341902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641669 | CCAAGGTATTTCAGT[G/T]TCTCACTTAACCCTT | 5607 |
rs571348743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795322 | AATGTATTAAACACT[C/T]AGCTCATAAATTTTC | 5607 |
rs571363170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682031 | TTTTAAGTGAACTGA[A/G]TGAAAAGCTGTATGC | 5607 |
rs571378224 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546834 | CTTTGGGAGGCCGAG[A/G]TGGGTAGATCGCTTA | 5607 |
rs571403593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684350 | TTAGAAGGATTATGC[G/T]TTAGCAGTGGGGCTA | 5607 |
rs571406629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649234 | TATTTTTTAAATGAG[A/T]TATTGGGCTTTTATT | 5607 |
rs571414450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785616 | AGACAACCCACAGAT[A/G]TCCACACCAACACAG | 5607 |
rs571416801 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663349 | TTGGTTGTCATGTCT[C/G]TCTAATGCCTCAGTG | 5607 |
rs571417596 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587701 | AACGTGGTTGTTCCC[G/T]CTTCCAGGTCAACAG | 5607 |
rs571421840 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549671 | GAGATTCAGACCTAC[A/C/G]TCAGTCTGACTCTCA | 5607 |
rs571448607 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547698 | CTGACCTCAAGTGAT[C/T]CACCCACTTCGGCCC | 5607 |
rs571452003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580102 | TAATTTGTGTTTACT[A/G]AGGAGTGTGAAAGCT | 5607 |
rs571458127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697575 | TTATTCTGCTCACTC[C/T]ATATATCCAGTACCT | 5607 |
rs571462954 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542272 | ACATTCAGATTCATG[A/G]CTTGACAAAGTGGGG | 5607 |
rs571464741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691768 | GTGTCATTACTTAGC[A/G]ACTGACTGCTTTGGT | 5607 |
rs571465246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786911 | AACAAGAGGGAAGAC[A/T]TTCCAGGGAGAGAAA | 5607 |
rs571467788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570571 | TTTTGACCACTGGGG[C/T]AGTTGTGTGCTCTGT | 5607 |
rs571491346 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549412 | AGAACTGTTTGTGTT[A/C]AATGTGGCATAATGG | 5607 |
rs571501647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674245 | TGCCATGTGTAATGA[C/T]GAGAGAGCTAGTATG | 5607 |
rs571508432 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615253 | TCTGCCCGCATCGGC[C/T]TCCCAAAGTGCTGGA | 5607 |
rs571528637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571428 | TTGAGGGGAAGGGAG[G/T]GGATACTGACTCAAC | 5607 |
rs571540755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781248 | AAATAGATGCAGTTC[C/T]TATCAATTATTAACC | 5607 |
rs571547637 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587423 | ATGGCCAGCCCTGTG[G/T]TTTTAAAAGATCCTC | 5607 |
rs571550146 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676155 | TGATTCACCAAGCCC[C/T]GCAGTTAGCTCTGAT | 5607 |
rs571591952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695464 | AAATTAACCTCTGAA[G/T]TCTTCATATCTGTTT | 5607 |
rs571596204 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696150 | TTTTTTTTTTTAACC[A/G]CAACTAGTTCTCATT | 5607 |
rs571602095 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541684 | AAAATACAAAAATGA[G/T]CGGGCACGGATGGCG | 5607 |
rs571619593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779289 | CCACTAGTAAAGAAG[C/T]TGATTTTAGCTTTTT | 5607 |
rs571634438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747613 | CTGCATTTATTCCCT[A/T]AAAATCAGTGTGAAA | 5607 |
rs571636963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675083 | CCGTATGACCCAGCA[A/G]TTGCATTCCTGGGCA | 5607 |
rs571650655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800065 | CAGCCTGGAAGGAAG[A/G]GTTGGCCCCAGGGAT | 5607 |
rs571659904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591406 | TTGAGATGGAGTCTC[A/G]CTCTGTAGCCCAGGC | 5607 |
rs571673086 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773806 | GAATAAACTGGTCTC[-/TT]TTTTTGGTCTCTGTG | 5607 |
rs571673841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738956 | CTATATCAAAATATG[A/G]GAGGTGTGAAGTAAA | 5607 |
rs571678570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585273 | CTAACCTGTAACTCA[A/G]GATGGTGTCAGGAAA | 5607 |
rs571679382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586200 | CTAGGTGCTGGTATC[C/T]ACAAAGATTTTAGTA | 5607 |
rs571683289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687313 | AAAAGCTGTATTTTT[A/T]AAATATGCACAGCCA | 5607 |
rs571695980 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678185 | TAGATAGATATATTG[-/T]TTTTTTTTCTTTTCA | 5607 |
rs571703438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633883 | AACAGGCAGAATTTT[A/T]AATTCTTAGAAGTGT | 5607 |
rs571728332 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555148 | TCTTTTAGGTCCTTA[A/T]TCTCCATTACATCTA | 5607 |
rs571729948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689330 | CAAATGGTACAGACA[G/T]ATGCTACAGAAATTC | 5607 |
rs571732178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771699 | GAAGGCAAATGTCCT[C/T]GATGTCATTAATGGT | 5607 |
rs571747468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605012 | AATAATAGAAAAATT[A/C]TTTACATTTTGTACT | 5607 |
rs571802341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739789 | CCTGGCCAATTTTAA[C/G]ATTATTTCCCTCCTT | 5607 |
rs571823331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598678 | ATGTCAGAATTATAC[C/T]ATTTGAACATGCTCA | 5607 |
rs571843744 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660281 | TGCCTCCAAAATGTA[-/G]GTGTTTTTTTTGTAT | 5607 |
rs571856756 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746969 | TGTCAAAATGGATAA[G/T]TTATCAACAATACCA | 5607 |
rs571857271 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740561 | TTGCACCACTGCACC[C/T]CATCTTGAGCAATAG | 5607 |
rs571862890 | snp | C/T | 0.000799041 | 0.019972 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626824 | AGGATCGCTTGAGCC[C/T]GGGAGTTCAAGGTCA | 5607 |
rs571874119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665541 | GAGAAAACAACTGAT[A/C]TTTTCAACTGTGATG | 5607 |
rs571906893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578147 | TGAGCATTTTGTCAT[A/G]GAGGTCACATGCTTG | 5607 |
rs571924824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633373 | AACACTGTTATAAAT[C/T]GTCTAGAAATCTATG | 5607 |
rs571938735 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583101 | CTGCCTATTAGGTAT[C/T]ACTGTTTCCAATTTA | 5607 |
rs571964534 | snp | A/G | 8.25593e-05 | 0.0064244 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703430 | TGTTTGCACATAGAC[A/G]CTTCTGTGCATATCT | 5607 |
rs571979986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771860 | CATCCGTGTGATTTT[G/T]CCAAGTGATAGAAGC | 5607 |
rs571990769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755439 | GACTCACATAGGTAG[A/T]AGTGTCTAGCTATGT | 5607 |
rs572024541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546388 | CAGAACCTGACACAG[A/T]TGCCAGAAGCAGGTT | 5607 |
rs572026418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554874 | TAAATGAGTAATTTG[C/T]GTTTTTGGATTATTT | 5607 |
rs572030723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799634 | CCAGTGGCCTTGCTA[C/T]GCAGAGGTGAACAAC | 5607 |
rs572070816 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745070 | AAGGGAAGAGGTTCA[C/T]CTATCAAAATGCAAC | 5607 |
rs572071412 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729637 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCACCT | 5607 |
rs572091785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640130 | TTCTTGCCTTACTCC[A/G]TGATTCCTGCAGATC | 5607 |
rs572136119 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556498 | GGGTTTTTATAAAAA[A/G]CATGTATTTTTATTA | 5607 |
rs572146630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575878 | TCTCTCTATCTCTGT[C/T]TCTGTTTTCTCTTCT | 5607 |
rs572151069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694470 | CTGTATATATTATCT[C/T]GATTAAAGATTTAGG | 5607 |
rs572153780 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647698 | AACATGGCGAAAACC[C/T]GTCTCTATAGAAAAT | 5607 |
rs572163566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554308 | AAGCAATCCATGCTC[C/T]TCAGCCTCTCAAAGT | 5607 |
rs572170555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640852 | AATAATGTACCATGA[A/G]TTTCTATTTTATACT | 5607 |
rs572180933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785211 | GGGCCTCTCAGAGTG[C/G]TGGGATTACAGGTGT | 5607 |
rs572186949 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770046 | TAAAACTGTCTTGTC[A/T]CTTAGTGGAAGCAGC | 5607 |
rs572187420 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556307 | GTTTAAAATTTTTAC[A/G]TGGTCAAACTTACTT | 5607 |
rs572194379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791977 | ATAAAAGTCAGGGCA[A/G]TTCTTACCTCCTACC | 5607 |
rs572197659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772483 | TTTAAGTGAAAAAGT[A/G]AGAAAAAGCTTTTTG | 5607 |
rs572202709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785780 | GCCTGGAGAGGCTAA[A/G]GATGGTCTTTCAAAG | 5607 |
rs572208512 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747979 | CTTTTGAAATGGATT[A/G]TGGTTTTTCTCCCTA | 5607 |
rs572224504 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804068 | ACAGGATCCTGTGAC[C/T]GTGTGGACCCTGCAG | 5607 |
rs572226464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687695 | AAATGGGAAAAGATG[A/G]AGCTCCTTCTCAGGC | 5607 |
rs572243662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577778 | GGCCAAGGCAGGTGG[A/C]TCACCTGAGGTCAGG | 5607 |
rs572247880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681602 | TTACTATTTCCAAAA[C/T]GATAGTCATCTCTTG | 5607 |
rs572288335 | in-del | -/TTA | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591372 | TAGAGTTAACAGGCT[-/TTA]TTATTATTATTATTA | 5607 |
rs572305092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792751 | TTCTTTTCCGCCCCC[C/T]GCTTTGACCATAAAT | 5607 |
rs572307189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578365 | TCTAGGCCTAGTGCC[G/T]TGTTGGTGGCTGTTC | 5607 |
rs572314129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779439 | ATAACCCTAAGAAAA[C/T]AGGCTTTGTTTTTCC | 5607 |
rs572347914 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695793 | GATGAATGTGATGCA[C/T]CCATCTGTTAATTGA | 5607 |
rs572357637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790942 | TTTTACAGAAGACGA[G/T]TCAGAGCTAGGGGGA | 5607 |
rs572381648 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752183 | CGATTCTCCTGTCCC[A/C]GCCTCCCGAGTAGCT | 5607 |
rs572387519 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67682223 | GTGTTTCTAGAGCTA[G/T]TTTTTTTTTTTTAAG | 5607 |
rs572388875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710134 | CCTGAGTAGCTAGGA[C/G]TACAGGTGCACCACC | 5607 |
rs572388994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718118 | AGCATGTACAGAGGC[C/T]AGAAGTATGAGAATA | 5607 |
rs572389240 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796139 | AACTAAGGCTCTATT[A/T]ATTGATTAATCATTT | 5607 |
rs572392015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590276 | GGTAAAATGTGATCA[A/G]ACTTGAAGTCTGAGA | 5607 |
rs572404433 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740724 | CAACTGTGTGATAAG[A/G]CTATCAGAAATGTGA | 5607 |
rs572410505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612141 | TATTTAAATCATTTC[G/T]GGAATCTAAATATTT | 5607 |
rs572423712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631294 | CTGTATCCCGTTAGA[A/G]TTTTTCCCTGAAATA | 5607 |
rs572451488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597212 | ACTACTTGGTATTGT[C/T]GTTGAATAAAAAGCT | 5607 |
rs572460206 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565523 | ATGAGCCACTGTGCC[C/T]GGCCTGTCATCATCA | 5607 |
rs572460949 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620078 | CTGTTGCTTAAAAAA[A/T]ATATACTAGTAGGCC | 5607 |
rs572500394 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593215 | ATCTCAGTTTTTAAA[A/C]AGTTAATCAGTTCTG | 5607 |
rs572500493 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562987 | GTTGGTTTTTAGTTC[C/T]GCTAACCAAACCTGT | 5607 |
rs572501733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731050 | AGTACAAAGGGCCAC[C/G]CATCTGGATCAGATG | 5607 |
rs572503035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787526 | TCACTCCTTCTTCTA[A/T]TGAGGTTATGACCAA | 5607 |
rs572539872 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572686 | TACTATATTTTGCAA[G/T]AATTGATATTATTAT | 5607 |
rs572541911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580960 | AGAAGTATTCATTAT[C/T]GTGGGGATTGCAGGC | 5607 |
rs572565264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568824 | ATCCTGACTAACACT[A/G]TGAAACCCCATTTTT | 5607 |
rs572582418 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541792 | AATCCGGGAGGCTGA[A/G]GTTGTGGTGAGTAGA | 5607 |
rs572586370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590634 | AGTTTTTAATTTTTT[C/T]TAGAGATGGGGCCCT | 5607 |
rs572588323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776817 | GGATGTGACTTAGCC[A/G]GGAGAACCTCCATCA | 5607 |
rs572595938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672233 | GATCCCTGAGGAATC[A/G]CCACACTGACTTCCA | 5607 |
rs572619822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684505 | CTGGATTACAATAAA[A/G]TCCAGCATTCAACGA | 5607 |
rs572620566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754646 | CCATCAGAGAGGAGA[C/T]GATATTTGAGCTGGG | 5607 |
rs572627261 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562326 | GGCAGATGATGTGGG[A/T]AAGTGATCAGGCCAA | 5607 |
rs572651679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568238 | AGTCCTTATATTTAA[A/G]TGAAGTGTAAGTATT | 5607 |
rs572666355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763324 | CAATGTTTTAACAAG[C/T]ATTGATTGAATTTGT | 5607 |
rs572735194 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658490 | CAGTGAACACACAGG[A/C]GAAGCCCAGTGCATT | 5607 |
rs572750460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663840 | TGATTGCACCACTGC[A/C]CTCCAGCCTGGGCAA | 5607 |
rs572763424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655789 | TTGGGGTCATTGTTT[C/T]CTGAAATATTCTTTC | 5607 |
rs572780756 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771127 | ATTCTTAAAACACAT[A/G]GTAATGTGTACCATG | 5607 |
rs572801021 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728527 | TATTATAGAAGGGTA[A/C]CAGCACTAAAATAGA | 5607 |
rs572805105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677154 | CTTCCCAAGATCACC[C/G]AACTATTCACTGCCA | 5607 |
rs572827737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628653 | CTCTGTGGATAAGAC[C/T]GTCATTCAGAAATAA | 5607 |
rs572828482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636910 | ACCTGCAATCTGGGT[A/G]GGCACCATCTAATCA | 5607 |
rs572832805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787052 | TGATCTGGAAGGGCT[G/T]TGCACACCAGAGAGT | 5607 |
rs572850064 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728094 | GGGTTCATTTAGAAA[A/T]CTCTATTGATTTTTG | 5607 |
rs572860040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781413 | GAGTCTTGTGGTTTC[A/G]GATACAGAGTTATTT | 5607 |
rs572891835 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661008 | GTATCTCTCTTTTCC[C/T]AAATTAACTTTATTT | 5607 |
rs572892213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720517 | TGAAATCTACTTTTT[A/G]TCATCTTTACCCAGC | 5607 |
rs572893950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772435 | GGATACATTTAATTT[A/T]AATTCATTCTTTATT | 5607 |
rs572907577 | in-del | -/GC | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576982 | CGCCCAGGCCGGACT[-/GC]GGACTGCAGTGGCGC | 5607 |
rs572924315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555852 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 5607 |
rs572929153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727512 | TACCCTCCATTTATA[C/T]TTGTAACTGAAAATT | 5607 |
rs572942272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667748 | GAGAAAAGAGAACAA[A/C]CTATTTCTCGCATTT | 5607 |
rs572964563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622532 | TAAATGCATGTGGAT[G/T]TTTTTTTTTGTAAAA | 5607 |
rs572975264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558570 | CAAAGTAAAAGACCA[A/G]GTCCTTAAAATGCCC | 5607 |
rs572975524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657031 | AGGACAAAATGAATC[A/C]GTGATGGCACAGAGC | 5607 |
rs572991574 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592411 | TTCAGAGAGGATAAG[C/T]AACTTGTCCCAGATC | 5607 |
rs573018357 | snp | C/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541097 | TTATTTTTCACAGAA[C/G]TGAAGTGCAGGTGAA | 5607 |
rs573020213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615283 | AATTATAGGTGTGAG[A/C]CACTGTGCCCGGCCT | 5607 |
rs573055912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767011 | ATATCTTTAATGAGT[A/G]ATTCTTTCCAGGGAC | 5607 |
rs573060571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802054 | AGGCTCGGAGCCTCC[A/G]TTCTTGCCCACAAGA | 5607 |
rs573077017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802879 | CATTTCACCCAAGCC[C/G]AGGGGAGGGACCAGC | 5607 |
rs573078042 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686033 | GAAGCAAATAGTAGA[C/G]ATTAGTGGAATGCTA | 5607 |
rs573078129 | in-del | -/TAAG | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721315 | ACTGTTTGGGCTCCT[-/TAAG]TAAGTTTATATCAGT | 5607 |
rs573081311 | snp | A/T | 0.000117197 | 0.00765407 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772776 | ATGTTTTTAGTTACA[A/T]TAGAATTCTCAGTTA | 5607 |
rs573091693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565551 | TCATTATTAAATTCT[A/G]AATAATTTGGGTTTA | 5607 |
rs573100588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623142 | GAGGTATATAGGTAT[G/T]TTTAGGGTAGCTTAT | 5607 |
rs573117259 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541122 | GGTGAAAAGGGGAAA[C/T]TCCTAGAATATCTGA | 5607 |
rs573118939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549877 | TAAACTCTGGGTTTA[C/T]GTTGCTGGGCTAAGT | 5607 |
rs573122830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621750 | TTATTTGTAAAATGT[A/G]CCTGATGTAGTTTTA | 5607 |
rs573136134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759288 | GTTAGGCCAGGCACG[A/G]TGGCTCATGCCTGTA | 5607 |
rs573138379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717611 | ATTTATTTACTCAGG[A/G]TTCTGTGGGTCAGGA | 5607 |
rs573138426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651393 | AGCATTGCAATTCCA[C/T]TTGTGTAGTTATTTT | 5607 |
rs573138797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660179 | TACAGCTGGAGTAGA[A/G]GAAATGTTTTTTAAT | 5607 |
rs573149942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801392 | GTTCATGAGTCCTTG[A/G]CCTCCTATCCCATGC | 5607 |
rs573151433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675468 | GAGGGAATGTTTACA[A/G]TGGAGCAAGATGAGG | 5607 |
rs573153503 | in-del | -/A | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720228 | TAGACAGATTAATAT[-/A]CACATACACAAACAT | 5607 |
rs573154311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613789 | AGTTTTTAATGGAAA[C/T]GGGTTAATATTTTTG | 5607 |
rs573212587 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600365 | TGGCATTGGTTATAT[A/G]CAGTACTGGAGACTG | 5607 |
rs573220201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767905 | TTGTTTTCTTTTCCT[C/T]TTAACCCTTCTCTAC | 5607 |
rs573247096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711665 | CACGCACACACAGGC[A/G]TGCACGCACACACAC | 5607 |
rs573260015 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547066 | CGAGACCCTATCTCA[A/G]AAAAGAAGAAAACAC | 5607 |
rs573273093 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67807025 | CTCCCAGGGTCCCTG[C/G]CCACTTCTGTTTTCC | 5607 |
rs573284730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690368 | TTCTGGTTGGTGGGG[A/G]GCATGTCAGAGAATA | 5607 |
rs573292241 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563694 | AAAAATTTTTCAAAA[C/T]CTACTTTCAACTGGA | 5607 |
rs573331464 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760883 | AAGTTGGATGCCAGG[A/G]TCAGTTACCCAGCAG | 5607 |
rs573348104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697042 | TGATTCAAACAGTAT[A/G]TGAAAAGGATGCTTG | 5607 |
rs573352377 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795399 | TAATATTGCTTTAGC[C/T]GCATCCAACAAGTAT | 5607 |
rs573352620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697305 | CAATCACTCTTCTTA[C/T]ATATATTAACTTTTA | 5607 |
rs573360459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587454 | TGCCTGTGGTGTGGC[A/G]AATGAGCAGAAGCTC | 5607 |
rs573398529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726735 | TAATCTTTGAAGTGG[A/G]TTGATGCTCTCTTAG | 5607 |
rs573410147 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804405 | GGGGTAAAGTATCGG[A/G]GATACAACATGCCTC | 5607 |
rs573416935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793472 | CTGCTGTTCTTGTTC[C/T]TCCCTTTAACACACC | 5607 |
rs573428067 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757904 | CTACCAGGGAAGCTC[C/T]GCAGAGGAGAGGAGA | 5607 |
rs573430417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705350 | TGGAGTTCCATTTGG[C/T]AAGGGCTGGGGCATG | 5607 |
rs573436528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587193 | CTGAGGTGGAGAAGG[A/T]GCTCAGCATGTTTGT | 5607 |
rs573461754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697835 | TGTAATCGAAAGCGT[A/G]AAATATAGAAAAGAT | 5607 |
rs573514562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607119 | GCTAGAATGATGGTT[C/T]GATTTATTTTGACTT | 5607 |
rs573521732 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789641 | ATTGCTTGAACCCGG[A/G]GAGGTGGAGGTTGCA | 5607 |
rs573530466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641883 | CAGTTTTAAAGCTCA[A/C]TCACAAGAATACACA | 5607 |
rs573536610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786604 | GCCGAGGGGCCGTAG[A/T]AGTCAGTGAGGATGC | 5607 |
rs573550993 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644092 | CTATTCTCATCACTG[C/T]CTTTTAAAAGTAAAA | 5607 |
rs573561833 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640228 | GTGACTGAGTGAATA[A/C]ATTTTTGTTCTTCTG | 5607 |
rs573566769 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799956 | GGGGGCGGTGGGGGG[A/G]ATTGTTATTGTGATG | 5607 |
rs573592343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601004 | AGTAAGTGTACCTTT[A/G]ACTGGCCTGAAGTTT | 5607 |
rs573595207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615244 | CTCAGGTAATCTGCC[C/G]GCATCGGCCTCCCAA | 5607 |
rs573601624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580307 | AGTCTCTGTGATTTC[A/G]ATTTCCATTATCTGT | 5607 |
rs573604525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741386 | CAGCAATTCATATTC[A/G]GTTCTCTCCTTAGTA | 5607 |
rs573624259 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664455 | ACAGTGAGCAGTGAT[G/T]GTACCCCACAGCACT | 5607 |
rs573644510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734651 | AAATTTAGACCACAG[A/T]TATCATTATCTTATT | 5607 |
rs573673082 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786945 | GCACAGGCTGAGACC[A/G]GAGGGAACAAGGACA | 5607 |
rs573681244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742040 | GCTGGGACTACAGGT[G/T]TCTGCCACCACACCC | 5607 |
rs573682536 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590366 | CTTGAGTCCTTTCTC[-/T]TTTTTTCCTTTTCAT | 5607 |
rs573687950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779354 | TGGATACTTGAGATC[G/T]CACTAAATCAGACAG | 5607 |
rs573692574 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608613 | TCATGGAGGAACTGG[C/T]ATTTGAGCTGAGAAG | 5607 |
rs573693740 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67540994 | CAAATCACAGGTTCA[C/T]AGAAAATCTCTAGTT | 5607 |
rs573696292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673481 | TTTATTAAATGGGAA[A/G]AGAGAAATGGTTTGG | 5607 |
rs573699061 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641731 | TCCAGTTTGAAACAT[G/T]TAGCACTTCCTAAGG | 5607 |
rs573712103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622459 | CAGTTAGAAATCTAC[C/T]CATGAAATGGAGATG | 5607 |
rs573715049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734054 | GGGAGCTTTGCCTTG[C/T]TTCAGCAGATTCTTG | 5607 |
rs573721961 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572578 | AATGTGCCCACCCTA[C/T]GTATGATGTTTGTTT | 5607 |
rs573724473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785716 | TGGAAGGAGGGGAAA[A/G]GTAGAAGGGTTTGTG | 5607 |
rs573752153 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581907 | TGAAGTGCTAAGTAA[A/G]TACAGTTGGGCTATT | 5607 |
rs573752619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605697 | GTTCTTCCCCCAGGC[A/G]GTGTTGTCTCAAGGT | 5607 |
rs573761109 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635464 | ACAGGTGTGAGTCAC[C/T]GTGCCCGGCCTGGAA | 5607 |
rs573763408 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571670 | TTTGATCTTCTTAAC[-/A]TCTTTATAAGATCAG | 5607 |
rs573767286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664939 | CTTAACTATTGTTAA[C/T]GCAAAACCTTTGCTT | 5607 |
rs573774575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628483 | AGACTCCATCTAAAA[A/T]AAAATAAAAATAAAA | 5607 |
rs573777585 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690625 | TGCAACCTCTGTTTC[A/C]CAGGTTGAAGCAATT | 5607 |
rs573784943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565463 | TCAAACTCCTGACCC[C/T]GTGATCCACCCGCCT | 5607 |
rs573789195 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631458 | TTTACTCTGCCACAG[A/G]TTTGAGAAGTCAAAT | 5607 |
rs573798168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780149 | CCACAAGTTAGTCCA[C/T]GTAGTACAGCGGCTC | 5607 |
rs573799779 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696129 | GAAAAGAGCTGAGCT[-/T]TTTTTTTTTTTTTTT | 5607 |
rs573814460 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733697 | CAGGGCTGTCAGGCC[A/T]GTTAGCTGAACAAAA | 5607 |
rs573832369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674409 | GTCCTTTAAATATAA[C/T]AAATATTAATCACAT | 5607 |
rs573837038 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574736 | GCTGGGCGTGGTGTC[-/G]GGCGCCTGTAGTCCC | 5607 |
rs573859037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800720 | TGTATCCCCCACCCC[A/G]ATGTACGTGATGGGG | 5607 |
rs573859320 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806925 | CCCCATGTGTGGCCC[A/G]CCCCACCAGGCCATC | 5607 |
rs573860411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713386 | TGTGATCTTCTATAC[A/G]TATAAGTAAACACAT | 5607 |
rs573878493 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651597 | CATTTGTTTTTGGCT[-/C]CCACATGTGAGTGAG | 5607 |
rs573881283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766320 | TCAACGGAAAAGCAT[A/C]TGGAAGAAAAGCCCT | 5607 |
rs573898130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806519 | AATGGAGCTGATAGC[C/T]TCCCTCGTTACCTCA | 5607 |
rs573908176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627342 | GTTAAATAATTCTTT[A/G]GTAAAGTAAACAGTT | 5607 |
rs573937716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620311 | GGGAGGCAGAGGTTT[C/T]ATTGAGCCGAGACTG | 5607 |
rs573945703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569922 | AGTCCTGTTTTATTT[A/G]AGTGGCAGGTTCCCT | 5607 |
rs573950485 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584455 | TCAAGGACCAGACGT[C/G]AAATGCATGTGACTG | 5607 |
rs573952315 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733073 | AGAGAGTAACAAATA[G/T]TTCATCCTGCCTTGT | 5607 |
rs573982601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570734 | TGAGTTCTTCACTGG[A/G]AAAACTAACAAATTA | 5607 |
rs573983962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774041 | ACATCTGCAGATCAC[A/G]CATACGCCCATAAAT | 5607 |
rs573985425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563771 | CTTAATATGGATACA[C/T]GATTTAAAGATGTAC | 5607 |
rs573998928 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626587 | ACTTATAAAATGTGT[A/G]TCACTTTGTACAAAG | 5607 |
rs574014607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666700 | CTGGGCCTGTACTTA[C/T]TTTTTCAGTTGGTGC | 5607 |
rs574031905 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710757 | GATCCACCCGCCTTG[G/T]CCTCCCAAAGTGCTG | 5607 |
rs574043791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620983 | AAAATATAAGTAGAG[C/T]AATATTAGCAGCTAA | 5607 |
rs574079038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771777 | AAAAAAGTATTGTCA[A/G]CAAATGCAGAGATTA | 5607 |
rs574085503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602084 | TTAAAATTGAGGTCC[A/G]ATGTGTCTAATGATT | 5607 |
rs574085873 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685298 | AAGATAATGGAAAGA[C/T]GTCTTTAAAATGTTG | 5607 |
rs574087396 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725065 | TGTCAGGAAATAACA[C/G]TGAAAGCAAAGCCAG | 5607 |
rs574087858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775800 | AAGGAAACAGGATGG[C/G]CAAAGCATGAGTGTA | 5607 |
rs574094013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668688 | TGTGAGAATGCCCTG[A/G]TAGTAACTGCTGTCT | 5607 |
rs574109647 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798254 | CCTCTGGGCATCTGC[A/G]TGGCCCAAAACTGCC | 5607 |
rs574117628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639746 | TTACATGTTTGAATC[C/T]TGTGTGTCTTTTAAG | 5607 |
rs574127120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775179 | TTGGCAGTTTTTGAC[C/G]ATGTCAGTCTTAAAG | 5607 |
rs574128410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765314 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 5607 |
rs574131152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704270 | TCTTTATTTTTTCTT[A/G]ATAGAGATAGGGTCT | 5607 |
rs574146315 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626204 | TTGGATTTACGTGGA[A/G]TAAACTTACTAATTT | 5607 |
rs574168357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661016 | CTTTTCCCAAATTAA[C/T]TTTATTTTCCAGGGT | 5607 |
rs574168867 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587992 | GAGTCTACTCCCTCC[A/G]TTCTTGGCCCATTCA | 5607 |
rs574186200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656133 | TAACTTTGGAATCAC[A/G]AGCAAAAAGTTCAAA | 5607 |
rs574217075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711537 | TTTAAAAGGAATTAC[C/T]GTTTGAAATGTTTAC | 5607 |
rs574230330 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669656 | ATTCTGGATATATTT[G/T]AAATGTATAGTTGAT | 5607 |
rs574233707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649299 | CTTGGCTCTTATCAG[A/C]TATGGGATTTCCAAA | 5607 |
rs574248368 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781429 | GATACAGAGTTATTT[-/G]GGGGGCCAAATCTGC | 5607 |
rs574253134 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797832 | GGATTACAGGCATGC[A/G]CCACCACACCTGGAT | 5607 |
rs574268676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705289 | ATGCCTGCTGTATAG[A/G]CAATGGGGATAGAGT | 5607 |
rs574276377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673888 | GAGTCTCACTCTGCC[A/G]CCCAGGCTGGAGTGC | 5607 |
rs574279559 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561981 | AAGCTTATTCTCTTC[A/G]TGATGAGAGATTTGT | 5607 |
rs574283558 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789637 | GAGAATTGCTTGAAC[C/T]CGGGGAGGTGGAGGT | 5607 |
rs574288194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599550 | ATTCAATTGGTGGAA[G/T]TTTAGAGTAGAGCAA | 5607 |
rs574288878 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671072 | GAAAGGCAGATCACT[C/T]CTGTTCTCTTTGCCT | 5607 |
rs574293267 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805761 | AGGAAGCCACTTGGT[A/G]TAAGTTCCTGGGCAA | 5607 |
rs574317302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613725 | CTCCTCTTCAGCTCC[C/T]TAGGGAAGCTTCTCC | 5607 |
rs574319126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648626 | CGCCTAGGCTGGAGT[G/T]CAGTGGGGTGATCTC | 5607 |
rs574345850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748712 | TCCTTGGAGCAAGTT[A/G]TGTTGTATGGCTCTG | 5607 |
rs574349902 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555807 | TTTTTTTTTTGAGAC[A/G]CAGTCTCACTCTGTC | 5607 |
rs574365833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559288 | AAGCTAGATTGTTTC[C/T]CTTGAAAGCCTTCTT | 5607 |
rs574367998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798363 | CCCTTTAAACAGGCC[A/G]GTGGCACAATTCTGC | 5607 |
rs574370596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641006 | CTGTTTGTTTGGTGC[A/G]GGTAGTCAAGACAAT | 5607 |
rs574384726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729676 | TGCTGAGGCAGGAGA[A/G]TGGCTTGAACCCGGG | 5607 |
rs574398349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607001 | TCTGGACCCAGCTTC[G/T]CTTGTGGCTGTGTTA | 5607 |
rs574405281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782775 | GATCGGCAACCCTGG[A/G]ATGCTGGTTTATGCA | 5607 |
rs574415259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761011 | CAGTACAAATGTTCT[C/T]AAAAGAGATTCCAAA | 5607 |
rs574434613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748025 | GAGGGTACTAAAAAG[C/T]GTTGTGTGAAATTAA | 5607 |
rs574457044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714815 | GCATTTAGGATTTCA[A/G]GTTTTTGGATTGGGG | 5607 |
rs574457133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722474 | AAGCACTTTAACACC[A/G]GTAAATTGCTGTTAT | 5607 |
rs574465923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608912 | CCTCACAGGGCCAGC[A/G]CGGTGCCTTACCTAC | 5607 |
rs574479264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617781 | ACTGTAGCATCAACC[G/T]CCCAGGCTCAAGTGA | 5607 |
rs574493316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721529 | TGGCTCACCCACTGC[A/T]CTAGAAGTCTATGAG | 5607 |
rs574496902 | in-del | -/CT | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737575 | AAAATCAATGAGTTG[-/CT]CCTAAAAGGAGCAAA | 5607 |
rs574502121 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669692 | TTGCTGATGGATTGC[-/T]TGTGACTTTTAAGAG | 5607 |
rs574520844 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632625 | CTCATCCCTCTGATC[C/T]TCATCTATCTTTTCA | 5607 |
rs574527544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608131 | CATTAGCGCACTTCT[A/G]TGTTGTAGGGTGTAA | 5607 |
rs574530557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709040 | AAAAAGATTATTCAC[C/G]TTGACTGATGTATGG | 5607 |
rs574552981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761665 | GGTTTTTCAGGACAC[A/G]GACCTGCCAGGTTCC | 5607 |
rs574554103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751837 | CCAACCATTTTGCCA[C/G]AGTGTTTGGCGCTGA | 5607 |
rs574557443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652895 | ACAGTATTTGTCTTA[C/T]TGTGTCTGGCTTATT | 5607 |
rs574568154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715659 | TTAAAAAAAAGCAAA[A/G]TCTTGATATGAAGAA | 5607 |
rs574587735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609640 | TAGACCTATTCTATA[G/T]GTCTGTAGATTCTGT | 5607 |
rs574588160 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745346 | GACCCAGAATAAAGA[C/T]AGGCATTCACAAAGC | 5607 |
rs574590399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708301 | ACACTCCAGCCTAGT[C/G]AACAGAGCAAGATGC | 5607 |
rs574596315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589607 | CATTCTATAAATGCA[A/G]TGAATCAAAATGTTA | 5607 |
rs574646073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629048 | CCCCTATGGTGGTGG[A/G]GGCCAATACTTTGCC | 5607 |
rs574662680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603578 | GAGAGGGGCGGTGAA[A/G]ATACCAAATTGCATA | 5607 |
rs574669080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752631 | TGCAGTGAGCCAAGA[C/T]AAGAGCACTGCACTC | 5607 |
rs574690085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644661 | GGGGGTCCTACCATT[C/T]CCAGGCTCTGTGGCT | 5607 |
rs574698075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706522 | TTTGATGCTCCTTGT[A/G]TTTTAAAATGGATGG | 5607 |
rs574709242 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636409 | TAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAGT | 5607 |
rs574714018 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668352 | ATAATTCCACATGAG[G/T]ACATAATCATTAAAA | 5607 |
rs574717469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743552 | TTTTGTTCTCTTCCT[G/T]TATTTAAAAGTGATT | 5607 |
rs574722886 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753671 | AGGATGGCTGTAATT[A/T]AAAAAAAAAGAAAAG | 5607 |
rs574727808 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776284 | TCTGCTTTTAAATCA[C/T]GCTGCTGCAACTCCC | 5607 |
rs574749192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601166 | CCCTGTGTCAACACT[A/G]TAAGTTATTAAAAAG | 5607 |
rs574755493 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721891 | AATGTAGATGGAAGG[C/G]TGTACACAGTTTGAT | 5607 |
rs574785116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629412 | TTTTTTTTTTGCACC[A/G]TGCTGTTGATTGCTA | 5607 |
rs574794807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604260 | ACTAATTTGGGCTAC[A/G]TGGAACATAAAGGAA | 5607 |
rs574810635 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782398 | CATTTTGGGGGATTG[A/T]TTTGAGGGCACCGAG | 5607 |
rs574821237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643268 | GTATTTTATGCTATA[A/G]GATTGAACTGATGCT | 5607 |
rs574836385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549961 | CCAGGTTCTCATATT[G/T]CCTGTAGGATTTGCC | 5607 |
rs574840706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558447 | TGGTCTCCCTGTTCT[A/G]CTTTTGCCTCTATAC | 5607 |
rs574845194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597097 | TGGCGTGAACCCGGG[A/G]GGCGGAGCTTGCAGT | 5607 |
rs574890777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782299 | TCGGGAGATTAGGGC[C/G]CCAGGGACAATGAGA | 5607 |
rs574892067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659216 | CTCATAAGTTCCATA[C/T]TTCACATTTATAATA | 5607 |
rs574927965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566191 | GGTCTTGTTTTGTTT[C/T]TGAGATGAAGTCTCA | 5607 |
rs574929928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781568 | AGGCCTTGGTCTACC[A/G]AGAGACATTTGCTGG | 5607 |
rs574933816 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551233 | ATAAAATGTGCAAAA[-/C]CTTTGACTTAGCAGA | 5607 |
rs574949485 | in-del | -/TGT | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627150 | GACAGTGTCTCCCTA[-/TGT]TGCCCAGGCTGGTCT | 5607 |
rs574970723 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593773 | AGACTCTTATTGATT[G/T]TCTTAACTGCTGTTC | 5607 |
rs574990507 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678398 | CTGCCTCCATTGTCA[C/T]CCCACAACAGCCACA | 5607 |
rs574993345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565741 | CCACTTTTTTTTATC[C/T]GAATAGAAGTCATCT | 5607 |
rs574997027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643740 | AGGCGTGAGCCACCG[C/T]GCCCAGCTGCAAACT | 5607 |
rs575001111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735371 | TTAGGTTCGTGATTC[C/T]TGTGTTGTTTGAAAG | 5607 |
rs575009549 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620418 | ATAAAGTATATACCT[A/G]TGAATTTAAATAACT | 5607 |
rs575010882 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667881 | ACAAACTCTTGAAAA[A/C]CTGGAGTCTCTCCCG | 5607 |
rs575022111 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704600 | AAAGTGTTGAACGTT[C/T]ATTAAATCATATTCT | 5607 |
rs575051481 | in-del | -/ATT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618014 | TCCTTACCTTTAAAG[-/ATT]ATTCTAGAAATTCAG | 5607 |
rs575054192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559463 | TTGGTTTTTCTTTTG[G/T]ATTGCATGTTGCCTC | 5607 |
rs575062613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581162 | AATTGTGGCTCATGA[C/T]GGTGGCCAAAGCTGC | 5607 |
rs575065545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735997 | GATAAAGGTCTAAAA[C/G]AGCATATTATATTTG | 5607 |
rs575072622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587988 | CTGAGAGTCTACTCC[C/T]TCCGTTCTTGGCCCA | 5607 |
rs575101368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573335 | CAGGAAACTTATAAT[C/T]ATGGCAGAAGACAAA | 5607 |
rs575102789 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557167 | AGGTGATAAAAATCA[A/T]CCGTGCCCACTAATG | 5607 |
rs575131510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699555 | CTGGGTATATGCATA[C/T]GTGTCCTAGGTTGGA | 5607 |
rs575163620 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590011 | TATTATTATGTTAAC[G/T]GGACTGATTTTAGGC | 5607 |
rs575174039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804374 | GCAGTGGGTCCAGGT[C/T]GCTTCCCTTGCAGGT | 5607 |
rs575175422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774259 | TACCCTGTTGTGTGC[A/T]GTCCCACATTTTAAA | 5607 |
rs575179176 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633147 | TTGGTTCTCACTGAG[C/T]GTGGCTCTGTTGTAC | 5607 |
rs575179205 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684668 | ACCAGAAATAATGTA[C/T]TTTGCAGACAGGACT | 5607 |
rs575183522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699849 | ACTGTATTTGACAGC[A/G]TATTGGACACAGCAG | 5607 |
rs575194849 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633046 | ACCTGTTACAGCCCC[C/T]ACATTTTACAGAGGC | 5607 |
rs575211240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757680 | AGTCATATATGCAGA[A/T]CACTAAACTGCAGGT | 5607 |
rs575220674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766293 | TCGTTCTTTACCTCC[A/G]TGCTTAGAAGTTCAA | 5607 |
rs575223749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767952 | TTTAGAATTGCTAAC[C/T]ATCCCTTCTTCTGGA | 5607 |
rs575224175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721468 | TTAGTTACAAGCTCT[C/G]AGACTACTTGGCACT | 5607 |
rs575226741 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600475 | ATGAAATGACCCAGG[C/T]AAACAAATTGTCATT | 5607 |
rs575233746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588816 | ATTTTAAAATGTTTT[A/T]ATTTTATTACTTTTT | 5607 |
rs575251890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581060 | GTTTTTGAAGTACAT[A/G]CTTACATTAGCTTAA | 5607 |
rs575253780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775106 | CAGAGTGGGCACTTA[C/G]GTGGTGAGGTCACTG | 5607 |
rs575254387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659491 | TTTCTAATTATTAGT[A/G]TGAAGTGCCCTGGGT | 5607 |
rs575271384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614474 | GCTAGTCAATCCTCA[C/G]GGTATTTCTATTTTC | 5607 |
rs575306751 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758133 | AACGTAGCCAGATTT[A/G]TGTTTTACACTGTGG | 5607 |
rs575309005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767164 | TTAACAGGCTACAAT[A/G]TCAGGTCTTAAATAA | 5607 |
rs575316316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609600 | GTAGATTCTGTAGAC[C/T]TATTCTATAGGTCTG | 5607 |
rs575335189 | in-del | -/TTTA | 0.00953873 | 0.0683987 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724387 | GAGAACTCGTTCTTT[-/TTTA]TTTATTTATTTATTT | 5607 |
rs575336888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660283 | GCCTCCAAAATGTAG[G/T]GTTTTTTTTGTATGT | 5607 |
rs575344102 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628631 | TTATAACCTTTGACG[A/G]CCATGACTCTGTGGA | 5607 |
rs575361998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649674 | AATGCGTATACATCT[C/T]GCATTGATCTAGTTG | 5607 |
rs575372463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551506 | CTTGGCTAATTTTTA[A/C]ATTTTATGTGGAGAT | 5607 |
rs575374039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758564 | TAACATCCTATAGGC[G/T]CTTGTAAATATTCAT | 5607 |
rs575388267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787110 | TTCTTAAGCAGGGAA[G/T]TGGCTGTTCAATGAT | 5607 |
rs575394506 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541182 | GCTATTGATTTACAG[G/T]AACTTAAAATGTGAT | 5607 |
rs575410288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623779 | ATTTTGTATTTTTAA[C/T]AGAGACGGGGTTTCT | 5607 |
rs575410454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616073 | TTTTCCTTTGTGCCA[A/G]TGCTATAAAGTCTTT | 5607 |
rs575416370 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550285 | AATCATATCTTGGGT[A/G]AGCATATTTCTACAA | 5607 |
rs575428134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609000 | CTAAGGATGGACACA[A/G]TGTGTTGTTCATTGC | 5607 |
rs575431350 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626609 | TGTACAAAGTATAAA[A/C]AATTATTTTGCTGGC | 5607 |
rs575446610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743713 | TGGAGGTTGTATGTC[C/T]CTAAGTTTTAATATC | 5607 |
rs575463271 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690317 | TAACTACTGGGGCAC[A/T]CTTGAAAGCACAACC | 5607 |
rs575465021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652816 | CCGCTCCCAGCCCCT[A/G]GCAAACAGCATTATA | 5607 |
rs575499951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713296 | GAATGTACAAGCTTA[A/G]CACATCTAATTTTTA | 5607 |
rs575516775 | in-del | -/CTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653747 | TTTTAGCTTGATGTT[-/CTC]CTTCTGTTTAAGGTA | 5607 |
rs575525821 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727056 | ATACAAAAATTAGCT[A/G]GGCATGATGGTGTGC | 5607 |
rs575541536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666492 | AAAATAATGTCTAGG[A/G]TCAGATTCTCACTAT | 5607 |
rs575547035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616891 | TAACACTCTATAAAT[A/G]ATTCACAGAGTAATT | 5607 |
rs575548063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787620 | ATTTAAAATTGCATA[A/C]ATTAATCTTAGATTA | 5607 |
rs575555793 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665369 | TGAGAAAGAGACTAT[A/C]ACAAAGCAACTTCAA | 5607 |
rs575561151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752535 | ATACAAAAATGAGCC[A/G]AGCCGGCTGGCAGGC | 5607 |
rs575577539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643966 | ATGTAATTCAAAGTT[A/G]AATGCTACATAACTA | 5607 |
rs575587483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657135 | ACCTCAAAATTAGAT[C/T]CCTTTTTGGCTTCTT | 5607 |
rs575589264 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669687 | AGAATTTGCTGATGG[A/G]TTGCTTGTGACTTTT | 5607 |
rs575646403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750309 | GTGGAAACTTGGGAA[A/G]TGAACATTGCCTTTG | 5607 |
rs575657811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608071 | TTTTATTTATAAAGA[C/T]GTTTAAAGTCCCCAG | 5607 |
rs575659211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760931 | GCTCTGCTTCACTGC[C/T]GAGTTGCTGTAATCG | 5607 |
rs575661356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705371 | CTGGGGCATGAGGGG[A/G]AGGACAGAGAACAAA | 5607 |
rs575664383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619182 | ATGGTGTGCCCCCAT[A/G]CTGCTCACATGTAAC | 5607 |
rs575668639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610962 | GTCTTGTGAATTTAA[A/G]TAATAAAATGAAAAA | 5607 |
rs575680226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657867 | ACATATGAAAATATT[A/C]ACATTTGCATTTCGG | 5607 |
rs575683185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755311 | ACATTGTTATAAAGT[A/G]GGCTCTTCCCTTATT | 5607 |
rs575683413 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746033 | AAGATTATAAAAAAA[G/T]ACTTTGATATTGCTG | 5607 |
rs575707733 | in-del | -/TAAG | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549888 | TTTACGTTGCTGGGC[-/TAAG]TGTGATTATGAGCTA | 5607 |
rs575751288 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767350 | GATCTTTATAGAAAG[A/C]CAGTCCAGAATTTTA | 5607 |
rs575781233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691461 | GTGGTACCCTTTTGC[C/T]GGATGGAAGGTCAGG | 5607 |
rs575782476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784495 | CCCTTCCACCTTGAT[A/G]CCACAGGCTGCATCT | 5607 |
rs575801213 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669292 | TAAGTAAGTAAAATA[C/T]GGAGTGTGTTAGAGG | 5607 |
rs575808244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684613 | CTATAACCGGGAAAA[A/C]ATCAATCTGTAGAAA | 5607 |
rs575821945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705949 | AAAAAATAAATTTAG[A/G]GAGGTAGCCAGGGGC | 5607 |
rs575834573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549891 | ACGTTGCTGGGCTAA[A/G]TGTGATTATGAGCTA | 5607 |
rs575841294 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730743 | AGGGACAGTGCCAGG[C/G]AATTGCTGCTGTGAA | 5607 |
rs575873208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692263 | TAAACTCTTTCTTCT[A/G]TAGAAACCAGAAATC | 5607 |
rs575901307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553363 | TTACGTTCTGTGATA[G/T]CATGCTCTTTCTTTT | 5607 |
rs575914690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633210 | CTGAGCTCCCTTTTC[A/G]CTAAGAGAAAACTTC | 5607 |
rs575930241 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677102 | TTAGCCTGTGAGTAT[-/A]AAGAACTTAAAACAT | 5607 |
rs575931786 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706212 | GCTAGGGGTACAAAG[A/G]TTAATAAAAAGAGAC | 5607 |
rs575940173 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635769 | GCTGTTTTCTTTCAG[C/T]TTTTTAAAGATTTTG | 5607 |
rs575944661 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710069 | GTCTTGCTAGGTTGC[A/C]CAGGCTTGCCTTGAA | 5607 |
rs575949640 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634750 | GGCTTCATTTTGACA[A/G]GTGTTAGCATGATAT | 5607 |
rs575956297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653830 | TAAATTTTCCTCTAA[A/G]CACGGCTTTAGTTGC | 5607 |
rs575967517 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761583 | AGGAGGACATACAGT[A/G]TGGTGATGTGGACTT | 5607 |
rs575973540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639887 | CTTTAACACCTTTCA[A/G]GGATCAGCTGAAAAG | 5607 |
rs575996980 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709175 | TATGGAATCATTAAA[A/G]GTCATTGCCACATAT | 5607 |
rs576010730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554084 | GGTTTTTTTGAAATG[G/T]TCTGGCTCTGTCACC | 5607 |
rs576027706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594826 | CCCTCAAAAACCAAA[A/G]AAACCCACCTTTGGA | 5607 |
rs576031134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717051 | GACTCATGGATTCAA[C/G]TCTGCTTCTTCCATT | 5607 |
rs576033653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734729 | CACTCTTTGAAAAGA[A/G]GTATTAGAATCTATC | 5607 |
rs576038983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616671 | TAGCCTTTGTTCACC[A/G]TTTTTCTTGTCTTCT | 5607 |
rs576052702 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633364 | GGAGAGGGGAACACT[-/G]TTATAAATCGTCTAG | 5607 |
rs576058089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556182 | TTTAAGGGTTTTCCA[A/G]TATTAAGGTTGGCCC | 5607 |
rs576060689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562169 | GGCTCTGTACGTTGC[C/T]CCAGACGTTTTTGGC | 5607 |
rs576074103 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566300 | ATGCCTCAGCCTCCC[A/G]GGTAGCTGGGATTAC | 5607 |
rs576075152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595922 | AATTTAAAAAGTGCA[C/T]AGTTACTCCAAAGAT | 5607 |
rs576094660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604952 | AAAAGGCTTAGCGCT[A/G]TGACTGACACTTATT | 5607 |
rs576094966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583903 | AGGCATGTGCCACCA[C/T]GCTGGGCATTTTTTT | 5607 |
rs576109375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804860 | CTGTCTAGGCAGCGA[C/T]TTGGGAAAGCAGCCG | 5607 |
rs576111331 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774002 | TGTTTCAATGCTGCA[A/G]TGAGTTGGCCACTTA | 5607 |
rs576112886 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797752 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 5607 |
rs576115718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662713 | TTAGGGTCATGGAAA[A/C]ATCTTTTTTTCAGTA | 5607 |
rs576116861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729759 | ACAGAGCAAGATTCC[A/G]TCTCAAAAACAAAAA | 5607 |
rs576141778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791804 | AATATAAGCATTTCT[C/G]TCTCCAAATCAACAT | 5607 |
rs576147551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589570 | TGTATTAGGAATCAC[A/G]TTTTATTTCTTGGAT | 5607 |
rs576152957 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582103 | AGTCTCGCTCTGCCA[C/G]CAGGCTGGAGTGCAG | 5607 |
rs576163051 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647583 | GAGATCTCATCTTTA[A/C]AAAAAAATTTTTAAA | 5607 |
rs576171584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738236 | GAAGCTTGTCTTGTT[C/T]TGTTTTCTGTTCAGA | 5607 |
rs576196731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561068 | CTCTATAGCTAGCTT[A/T]GTTGCAGAAATGAGA | 5607 |
rs576229758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730201 | GGAAAGGATACTTTA[G/T]AAATGCCTTTCCTAC | 5607 |
rs576230422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799534 | CAAAACCAGCTGACA[C/G]ATGAGACCCAGAAAT | 5607 |
rs576232516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597936 | AGGCCGGGCGTGGTC[A/G]CTCATGCTTGTAATC | 5607 |
rs576233465 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697040 | GATGATTCAAACAGT[A/T]TGTGAAAAGGATGCT | 5607 |
rs576233876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722731 | TTTAAAGTTTCCCTG[G/T]GTCTGAGTGTTCCAA | 5607 |
rs576242713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750102 | TAAAATATCTTACTT[C/G]TTTAATTTGGGCAAA | 5607 |
rs576271556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546241 | TCAGCATCTCTGGCT[G/T]GGAACCTTAAACTTT | 5607 |
rs576282346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584797 | CATTCTCCTGCCTCA[C/T]GACATTCTCCTGCCT | 5607 |
rs576288259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590930 | ATAGAATACGTAAGA[A/T]GTGTCTGTGTTCTCA | 5607 |
rs576294395 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722892 | GACTATAAAGTTGTC[A/G]TTCAGCTAGATCACT | 5607 |
rs576303475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632481 | ATTAGGAGACTGAAA[C/T]TCAGAAAGCTGAATT | 5607 |
rs576308292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688719 | AATCCTCACAGTTCT[C/T]TAATATTGACAAGGT | 5607 |
rs576322954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618733 | CCTTTACCCACAAAT[A/C]TTGTGGGTTCTTCCT | 5607 |
rs576323912 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710124 | TCCTCAGCCTCCTGA[G/T]TAGCTAGGACTACAG | 5607 |
rs576332385 | snp | A/C | 0.000132181 | 0.00812854 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703313 | CATCCGTCCACTCAC[A/C]GGCTCCCTTCTGATT | 5607 |
rs576345961 | snp | A/G/T | 4.96852e-05 | 0.00498403 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693509 | CTAACAGACTGTTTT[A/G/T]TCTCATAGCTGGTGA | 5607 |
rs576350295 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559806 | CTGCTCCCCTACCCC[C/G]ACCCCTTTTGTTGGT | 5607 |
rs576363163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585499 | ATCCTTTTCTCACCC[C/G]GCTTGCTCACAAAAA | 5607 |
rs576386675 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587391 | AGCAGTTAGAGGGCT[A/T]TTAGTAGGAGAGGGA | 5607 |
rs576394811 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773803 | CTAGAATAAACTGGT[C/G]TCTTTTTTTGGTCTC | 5607 |
rs576400943 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582891 | ATTTGTCTCTAAAAA[A/T]TTTTTTTTAGTTATC | 5607 |
rs576403740 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741642 | TTCCCATGGAACACA[C/T]GGGCTTCTTGGGGGT | 5607 |
rs576414474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769742 | CTCCGTGAGACCTTA[C/T]GGCTCTCCCTGCATC | 5607 |
rs576443839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543884 | AGGGAAAAAGGACAA[C/T]TTTAACTTACCATGT | 5607 |
rs576454058 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800609 | AATGACCAATTGTTC[A/G]TATGAATCGTTTATG | 5607 |
rs576466354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776816 | AGGATGTGACTTAGC[C/T]GGGAGAACCTCCATC | 5607 |
rs576484741 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686414 | GAGTTCGAGACCAGC[A/C]TGGGCAACATGGTGA | 5607 |
rs576492001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653661 | TTCTCTATTTTTTTT[C/T]CTATTCTCTGTTTTG | 5607 |
rs576512210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637194 | CTCCTCAGCTTGCAG[A/G]TGGCCTATTGTGGGA | 5607 |
rs576538072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624913 | TGGGATTACAGGCAC[A/G]AGCCACTGTGCCCAG | 5607 |
rs576546667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575803 | TGTAGATATGTAGTG[A/C]TGAGCCTAACACACA | 5607 |
rs576565802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679594 | AAATATTTGTAATTG[C/T]GGTTTATCAGGCCTA | 5607 |
rs576580573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624271 | GTGAACCCGGGAAGC[A/G]GAGCTGGCAGTGAGC | 5607 |
rs576587068 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677761 | TAGAAGGAAATCTCT[G/T]TTACTTACTATGAAA | 5607 |
rs576603882 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775993 | ACCACACTTATCCAC[A/C]TGGATCTTTTTTCTT | 5607 |
rs576625450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782968 | TGGAAAGTGGGTTAA[A/G]CACCGAAGGAAGGTG | 5607 |
rs576630374 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674281 | TCTTCCTTCCCTGAG[C/T]TCTCAGGCTGTTTAA | 5607 |
rs576630686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645751 | AGAGATGGGTTCTCG[C/T]TATGGTGCTTAGACT | 5607 |
rs576633332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662157 | TAGCAAATCTTTCAG[A/G]AGCACATTGCACCCT | 5607 |
rs576636392 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546085 | GCCTGACGAAGGACC[C/T]GTGGCAGTGGGTGTT | 5607 |
rs576640735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770450 | ACTCCAGCACAGAGA[A/G]TTACCTAGGAGAGAG | 5607 |
rs576641661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716472 | TCTCAACACTAAAAT[C/T]CTGAGTCTATGATAA | 5607 |
rs576655692 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637672 | CTCTCTCCCTCAGGT[C/G]CTCTGCCAGCTCTCT | 5607 |
rs576664175 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640012 | CTGTATATGTCTTTT[A/C]AGGGTGTTATCACCA | 5607 |
rs576665467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769795 | CGGGGCCTTGGGCAG[A/T]TGGGGCAGCAAAGCT | 5607 |
rs576679002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583859 | CTGGAGCAGTTCTCT[C/T]GCCTCAGCTCCTGAG | 5607 |
rs576700504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776742 | TTTGCTTCTCTAAAC[C/T]ACAAGGAATTCCTTC | 5607 |
rs576726684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560309 | AGTCTTCTCATGGGT[A/G]TGGTTACTTTTCTAA | 5607 |
rs576737937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618519 | CTGTGTCCTGAACTT[C/G]AGACTCATATCTGAT | 5607 |
rs576739497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567994 | CTTGCTTTTGTAAGT[A/G]GATTTATATTTGTTT | 5607 |
rs576747362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791039 | CTACCCAGAGAGAGC[G/T]CCTCACGCCATGAAT | 5607 |
rs576751863 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637643 | TCCAGGACCCCCTCG[A/G]CAGACCTCTGGAGCT | 5607 |
rs576764866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670969 | CCTGTTGGACAATTT[C/T]AAAAGCTCAGTTTCT | 5607 |
rs576765494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646649 | TTAAATATTTATAGC[C/T]GAACTGTAATTTTAA | 5607 |
rs576768976 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804312 | CCCCTGTGATTCTCC[C/T]TGTCAGGCAACCACC | 5607 |
rs576782437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67671990 | CTACAAAGGACATGA[A/G]CTCATCATTTTGTAT | 5607 |
rs576783839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552560 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5607 |
rs576797158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560974 | ATATAAGCACTTGCC[A/C]ATCCTATGTGAACAA | 5607 |
rs576817499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753822 | AAAGCTAAAATAGAA[C/T]AATTAAATGACCCAG | 5607 |
rs576843031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671301 | ATGAAAATAATAACA[A/G]TAATGACTATTAAGC | 5607 |
rs576843588 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685619 | AGCTTATAGTGTACA[C/T]AGAAGAAAGATGTAT | 5607 |
rs576846430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804820 | AGAGGAAGTGTGCAC[A/G]CTTGGACTTTGGGAA | 5607 |
rs576869910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602031 | GAAATAAATAATAAC[A/G]TGTTTCTTACATGTT | 5607 |
rs576873922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707238 | TTTTTTCTTAAGGGT[C/G]AATATAATGAGAACA | 5607 |
rs576881274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708518 | TTTTTTTCTAGAGAC[A/G]TGGTCTTGATATGTT | 5607 |
rs576886678 | snp | A/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722001 | TAATTGTCTTTAATT[A/T]AAGTGAATTAGATTT | 5607 |
rs576896685 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662021 | TGTCTTCCTGTCCAG[A/C]ATACATGTGTTTTAT | 5607 |
rs576917660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736034 | TTCCGGTACTTTAAC[A/G]GTACTACCATTGTTA | 5607 |
rs576941932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595707 | GTTATCACTTTATGT[A/T]GGAGTAATTCCATTT | 5607 |
rs576946690 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682840 | TCCATCTCAAAAAAT[-/A]AAAAAAAAAGAGTTG | 5607 |
rs576970549 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677100 | AATTAGCCTGTGAGT[-/A]TAAAGAACTTAAAAC | 5607 |
rs576984487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623886 | ACAGGTGTGAGCCAC[C/T]GCCCCCGGCTACTTC | 5607 |
rs576999383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709123 | GTTTTTAACTCACAT[A/C]TTTAAATGTGTTGTA | 5607 |
rs577009844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583934 | TTAATTTTTTAATAG[C/T]GACAAGGTATCACAG | 5607 |
rs577010106 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798402 | AGGATCAGCTTCCTC[C/G/T]GACAAACTCATGAGT | 5607 |
rs577011538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567406 | TCTGTCGCCCAGGCC[A/G]GACTGCGGACTGCAG | 5607 |
rs577017568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603615 | TGTCATTGATCATTG[A/G]GCATCATTTTTGCTC | 5607 |
rs577022557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590865 | TATGGAACCCTTAGC[A/G]TATGCCAAGTCATTG | 5607 |
rs577048045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629515 | TCTGCTAAACAGCAG[A/T]AAATGATGTTTCCAT | 5607 |
rs577049766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631420 | CTCACTGTACTTTCG[G/T]TCTTTTCTTTTCCTA | 5607 |
rs577069543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695033 | CAAACACCACATATT[C/T]TCACTCATAGGTGGG | 5607 |
rs577080618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590344 | ATATGTGTATTTCAT[A/G]TTAGGTCTTGAGTCC | 5607 |
rs577086283 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776569 | AATAATCAAATGGAA[A/G]GATGCAAAAACATAA | 5607 |
rs577095582 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67716957 | ATTTTGCAAATGAGG[A/C]AACTTAGATCCAGAT | 5607 |
rs577096224 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782516 | TTTTTTTCAGCGCCT[C/T]ACAGTAGGCGCCTCT | 5607 |
rs577099268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745902 | TCAGGTACTGGCACT[A/G]TTACCTTAATACAAA | 5607 |
rs577110678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624210 | CAGGCGTGCTGGCGG[A/G]TACCTGTAGTCTTAG | 5607 |
rs577136285 | in-del | -/T | 0.0314385 | 0.121371 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594754 | ATTAAATAATATGGC[-/T]TTTTTTTTTCTTTAT | 5607 |
rs577151189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729712 | GAGCTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 5607 |
rs577154433 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692830 | CTTTGATATGAAAGC[A/G]TTTTGGCCAGACAAA | 5607 |
rs577157490 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713586 | ACTAAAAATACAAAA[A/G]TTAGCTGGGCATGGT | 5607 |
rs577161391 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632661 | CATCTCCAATATGCC[-/T]TTTTAGCTATCCACA | 5607 |
rs577186321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751917 | GCTAACATGCCTTAC[A/G]TGGCTGTACTGCTCT | 5607 |
rs577197719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599412 | AGGATTGGTAAAATG[A/G]CTTGGAAAAGAAGCT | 5607 |
rs577198087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591663 | CATGAGCCACCGCGC[C/T]GGCCCCTTAACAGGC | 5607 |
rs577201347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738139 | TTACAGGCGTGAGCC[A/T]CTGCACTTGGCCTAG | 5607 |
rs577211305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609513 | GATTCTGTAGACCTA[C/T]TCTATAGGTCTGTAG | 5607 |
rs577219094 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744768 | AAGCAAACTTCTACA[G/T]TGGCAATTTCCTTTC | 5607 |
rs577225127 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744267 | AAAATTTGAAGTTTT[A/T]AAAAAAAGAATAAAG | 5607 |
rs577226101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597926 | AAACACAGTCAGGCC[A/G]GGCGTGGTCGCTCAT | 5607 |
rs577233841 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543774 | TGAATCTAGAAGAGA[A/G]GTTTTTTCCCCCCAA | 5607 |
rs577240945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737636 | CAGGACACACCAGGT[A/G]GAAAGAGGGTCCCAG | 5607 |
rs577253784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637093 | CAGTGATTTGCCGGG[A/G]GCTTTCAGGCCTTCA | 5607 |
rs577260372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598762 | GCAGACTGTGGCCCC[C/T]CCAGAGTGTAGACTC | 5607 |
rs577268960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704030 | CAACTCTTTATAGCT[A/G]TATTTAGAATGGACT | 5607 |
rs577312249 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651936 | TTTTTTGAGGAATTT[C/G]CATACTGTTTTCCAT | 5607 |
rs577318626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543796 | TCCCCCCAAGTGTTT[C/T]GGGGAATGTCCTTGG | 5607 |
rs577340213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582789 | TTGTGCCACTGTACT[C/T]CAGCCTGAGTGACAG | 5607 |
rs577359168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782906 | TCCTGCCTTCAGAAA[C/T]GGCCCCCTTTTCAGC | 5607 |
rs577360962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728015 | AGGTGCAGGGAGCAA[C/T]TGTGAACATTTGAGC | 5607 |
rs577362388 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568136 | TCACTCTTTATATCA[-/T]TTTTTTCCCACATTG | 5607 |
rs577372584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729147 | GTGAGATTTTAGTGT[A/G]TATAGCCTTGCTGCT | 5607 |
rs577408034 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693357 | TCAAAAGAAAAGAGA[G/T]ATTTAATCATTTTTA | 5607 |
rs577421155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733951 | TGAGAGGAGCTGTAG[A/G]TGGCATTTGCTTCAG | 5607 |
rs577422123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669736 | TTGCTTAAATTGTTA[A/C]CAGTTTAGTATGCTA | 5607 |
rs577434879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788897 | GGATCACTTGAGCCC[A/T]TGAGGTAGAGGATGC | 5607 |
rs577435985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776464 | TGGGAAAAAGCCAGC[C/T]CCTTGCCAGTCAGAA | 5607 |
rs577477314 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582320 | TCCCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 5607 |
rs577484922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574386 | AGACCAGCTTGGCCA[A/G]CATGGTGAAACCCCA | 5607 |
rs577488242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765566 | CAAAAAAAGAATATT[C/T]CTTGAATATTAAAAG | 5607 |
rs577515377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621865 | AAATTAATAAATTTT[A/G]TCAGGTGTTGCTAAC | 5607 |
rs577549095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574853 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 5607 |
rs577550879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789667 | TTGCAGTGAGCCGAG[A/G]TCGCACCATTGCACT | 5607 |
rs577552912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685342 | ATTCCAGAATTCTGT[A/G]CCCAGCAAATACATT | 5607 |
rs577553691 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548069 | CATGTGCAGTGCCTT[A/G]TTTATGTCGATGGGC | 5607 |
rs577566815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608963 | TTCAGGAATTTACCT[G/T]CAGAGGCAGATTCTT | 5607 |
rs577568568 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640150 | TCCTGCAGATCCTTG[C/G]ATATAGGGTATAGTA | 5607 |
rs577586852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576796 | GATAGAAAGTTTGCT[A/T]AATATTGTTTCAATA | 5607 |
rs577590812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680760 | GATTTATTGCATCAT[C/T]GTTAAAAAGCCCAGC | 5607 |
rs577591945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695877 | TGCTTTGCTTCTTAG[C/G]TGAGTGAATTCTAGT | 5607 |
rs577592443 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575125 | GGTTATGTTTCAGAA[C/T]TTAGGAGAGAAATCT | 5607 |
rs577600126 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793038 | GTAGTGTATTCTTTA[C/T]AAAATCAAACTTTAA | 5607 |
rs577606814 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761861 | TTTAATCAGCACTTC[C/T]GTAGAACCAGCTGAA | 5607 |
rs577608040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606051 | CATATGGAAATAAAA[C/G]TAATTAACAGGCATA | 5607 |
rs577612961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800452 | TACACACAGCTTATT[C/T]CTGTATATTGTCTCA | 5607 |
rs577623095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586651 | AATGGAATAATGACA[A/G]GAATAGAATATTATG | 5607 |
rs577629727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679428 | GAAAATCAGAGCAGC[C/T]ACTTGCGGTTATTGA | 5607 |
rs577647182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569028 | AAAAAAACAAAAAAA[A/C]AAAACAAAACTCTGT | 5607 |
rs577650927 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555482 | ACCATATCATTGTGG[A/G]AATAAATTTGTAAGA | 5607 |
rs577658685 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741295 | ACTCAAAGGAGCCCT[A/T]ATCACAAGGGGAAAT | 5607 |
rs577700329 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706282 | TGGGTTCTGTTGATG[A/T]TATTCATTTATCCTG | 5607 |
rs577713681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648563 | AGTTTTTGTGTGGAC[A/G]TACGTTTTCAGTTCT | 5607 |
rs577717862 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649962 | CTTAACATTATTTAA[C/T]CTTCCACTCCGTGAA | 5607 |
rs577724576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628077 | ATGAATGCAAGGCCA[C/T]GCAAGGTGGACGGAA | 5607 |
rs577729293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681422 | CACAGTCAGTATGCA[A/G]CGGCACCTTCCAGGG | 5607 |
rs577733232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579275 | CTTGTGTGCCGAGGA[C/T]AAGTCATTTTCGGAC | 5607 |
rs577743569 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605376 | GACTCTTTTTGATAA[A/G]CATCTCACAGAATTA | 5607 |
rs577766371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710661 | GGCATGCGCCACCAC[A/G]CCCGGCTGATTTTTG | 5607 |
rs577784943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635055 | TATTGTACCACTTTA[C/T]AGTCTACAAATCTTA | 5607 |
rs577794450 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547278 | TCTTCCTAAAGTCAA[A/G]GATCAAGTTTTATTG | 5607 |
rs577798966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690279 | AACATTTAAGTGTCT[A/G]CTGTGGCTATGATGT | 5607 |
rs577804687 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645083 | AGCCCATGAGACAGA[A/G]GTTGCTTGAACCCAG | 5607 |
rs577822580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665965 | CGCACACCCAGCTAC[C/T]GGTAAAGTGGTGATA | 5607 |
rs577827145 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603213 | TAATCGAAACTCTGC[-/A]CCCATTAAACAGTAA | 5607 |
rs577842598 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657070 | TAAAGATTTAGCCAT[A/G]TGGATAGTTAAGGAA | 5607 |
rs577844824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719718 | GTAGGCTGGAAATCT[A/G]TCTACTCATCTGTTG | 5607 |
rs577853424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640940 | CATTTTAAAGATAAC[A/T]ATTTCATAATGACCA | 5607 |
rs577881659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772542 | CTGACTAAGTAAAGA[C/T]CAAAATAAAAGAAAG | 5607 |
rs577882113 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570825 | ACATATAATAGGGTA[A/T]GCTTGCAGTATTGAC | 5607 |
rs577903989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711411 | AAGCTATAGAACCTT[C/T]GGTAAATTACTTAAC | 5607 |
rs577912337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569726 | AAAGATAAGCACGAG[C/T]AGGCCTCAGTCTTGG | 5607 |
rs577923503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724311 | AATATTCACTTGGAG[C/T]ATATGTGCTCCTTCT | 5607 |
rs577930481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703533 | ATAGATGTATACAGA[G/T]TTTGACCATAAAGTC | 5607 |
rs577965108 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653561 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 5607 |
rs578001569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687732 | CATGCTCTTCTGGAT[C/T]GGCATGTTAGTTCAC | 5607 |
rs578002096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663137 | CTTTATCCCCAAATA[A/T]GTTAGGTATCTATTT | 5607 |
rs578010222 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675507 | TGGTGATGGAAATGT[A/T]CTCCATCTTGACTAT | 5607 |
rs578017364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717286 | AGAAACTAAGGCCTA[G/T]TTTATTTATTAAAAA | 5607 |
rs578026153 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771183 | ATGTGTTTTACACAT[A/G]GTAATGTGTACCATG | 5607 |
rs578032156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725008 | CTTACAAGCAGTCCT[C/T]CCAGGAACATAGTTA | 5607 |
rs578032337 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598530 | CCTCCTCCCTGCACT[C/T]CTTCCCCGCCTGTGC | 5607 |
rs578042217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770585 | CCAGAGTCATGTCCA[C/T]TGGTGGAAAATGAAT | 5607 |
rs578043271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625943 | GGTATGTATATTAGA[C/G]TATCTGCTAATCATT | 5607 |
rs578043951 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67672868 | GGGATCCAGTTTCAG[C/T]TTTCTACATATGGCT | 5607 |
rs578056463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584717 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 5607 |
rs578065123 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631719 | GCATCCCAGTCCTGC[C/T]ATGCCACTTTGGATT | 5607 |
rs578072749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731329 | GTGTTGGGAAGATAC[G/T]AGGGACAGTCAGTGC | 5607 |
rs578086802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806027 | CACAGGGCAACAGGG[A/C]CGGCCCCTCCAGAGT | 5607 |
rs578102668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612816 | ACTGTTCAATTAAAG[C/T]ACAGGCATTTACATG | 5607 |
rs578106757 | in-del | -/AA/AAA | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541857 | CGAGACTCCGTCTCA[-/AA/AAA]AAAAAAAAAAAAAAA | 5607 |
rs578135833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67612226 | TTTCTGCTTTCTCCT[A/G]TCTATCATATTTTAA | 5607 |
rs578167489 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766316 | AAGTTCAACGGAAAA[-/G]CATCTGGAAGAAAAG | 5607 |
rs578175511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799801 | GCAGCAGTACTTCCA[C/T]ATAGAATGAAGCCAG | 5607 |
rs578192414 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550831 | GGCTGGAGGGCAGTG[A/G]TGCGATCTTAGCTCA | 5607 |
rs578202988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605611 | ACCACTGAAAAAACT[A/G]GGGCTTATCATGTGG | 5607 |
rs578203396 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764209 | GAGAGGTTGTCCCAT[C/G]TTCCTTTGCTTTACT | 5607 |
rs578206780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763392 | AACGAGACTCATTCT[C/T]GGACCAGGAGCACCT | 5607 |
rs578219577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655145 | TTATGCTATTATTGT[C/T]ATATAAGTTACATTC | 5607 |
rs578239966 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735058 | CCATAAAATGCAGAG[A/T]CGAAATTTAAGTGAC | 5607 |
rs745315367 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643355 | TGTTGGCAAGTGACT[A/G]TTGATCAGGAGAAGT | 5607 |
rs745346937 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740299 | TACTTTTTACATGTT[C/T]GCAATCAGAGGGAAC | 5607 |
rs745349682 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753953 | AACGTAGAAAGAATC[C/G]AGAAGTTCACATTGG | 5607 |
rs745350875 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610872 | TGACCCTAAAATTTC[A/C]TTACTTTTCCTTGTC | 5607 |
rs745359292 | in-del | GTTGATAAC/TGATAACACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756563 | TGTGTGTGTGTGTGT[GTTGATAAC/TGATAACACTT]ACGATCTACTCCCTT | 5607 |
rs745371794 | in-del | -/AGATAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779553 | TAGCAAGAGAGATAT[-/AGATAA]AGTCTGTCATTCCTT | 5607 |
rs745380979 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771983 | CATGTGTGAGTGCTT[C/T]ATCACATAGCTAAGT | 5607 |
rs745395176 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644416 | ATAAATAAATAAATA[A/C]AACAATTACTCTTGA | 5607 |
rs745415721 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707710 | GGGGTTTCACACAAA[A/G]GAATTGACATTTAAG | 5607 |
rs745417790 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743269 | GTTGGTTCCTTCTTA[C/T]AACCTACTGAGTAGC | 5607 |
rs745419455 | snp | G/T | 1.84889e-05 | 0.00304041 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806810 | AACAACCCACCCGTC[G/T]CCCTTCTCCGTATGC | 5607 |
rs745436620 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741815 | TATATGAAGAGCTGT[C/T]ATTAAACTTATATGC | 5607 |
rs745452650 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580818 | CTCTGCAGATATTTC[C/T]AAGAGGTAATGTTGA | 5607 |
rs745459985 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753007 | TATAGGATAGACATA[C/T]GGAATAGAATTCAAA | 5607 |
rs745470139 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576231 | CTTCTCTCTTTCTTA[A/G]TAGAAAATTTGTGCC | 5607 |
rs745489686 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543046 | CTTCACCATAGCGTT[C/T]GCTCAACTCCAGAAC | 5607 |
rs745519426 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67693553 | GACGTATGTTGGAAC[A/G]AATGCTTATATGGCG | 5607 |
rs745520265 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718151 | AGCTGTTTATGACTC[C/T]CTTGACTTTGAAATG | 5607 |
rs745525225 | in-del | -/CTGA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637301 | TCCCTCTAGAGAACC[-/CTGA]CTAATACAGAGATGG | 5607 |
rs745567679 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656716 | TGGCTTTAGCTAGAA[C/T]ATTCACATCACTGGG | 5607 |
rs745579352 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623760 | CCACCACCACACTGG[A/G]CTAATTTTGTATTTT | 5607 |
rs745586256 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795162 | TGGATTTGTGGTTAT[A/G]TATCTTTTTTCCCTT | 5607 |
rs745599690 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790216 | TTTGTTTTAAGCCTG[A/G]GAAGACTGTGTGGTT | 5607 |
rs745616330 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785854 | CTGGGAAACTGGAAA[A/G]AGATTGAATTGGATG | 5607 |
rs745631922 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760681 | CCATGAAGCCTGATG[C/T]ATTATTAATGAATTA | 5607 |
rs745638920 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585633 | TTTTAGCTCAGTTAA[A/C]TTGATTTTTATATGT | 5607 |
rs745644183 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633032 | AGACCTTGGAGATCA[C/T]CTGTTACAGCCCCCA | 5607 |
rs745683846 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604879 | TAGCCTGGCAACAGA[A/G]CAAGAAAAAAAAATT | 5607 |
rs745688224 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701540 | TAGGAGTAGAGAAAG[G/T]TTTCACCCTCAAACA | 5607 |
rs745695340 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571694 | AGATCAGCAAGGCAG[G/T]TTTTTTCCCCATTTT | 5607 |
rs745697777 | in-del | -/GAAAAAAAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714414 | TACCCAGCTGCCAGG[-/GAAAAAAAA]AAAAAAAAAAAAAAA | 5607 |
rs745706923 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619500 | GGAGGAGAATATATC[A/G]TATACTGTGGAAGAG | 5607 |
rs745711499 | snp | A/G | 3.29957e-05 | 0.00406162 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600689 | TTCTTGTGGAGATGA[A/G]TGAACAAGACATACG | 5607 |
rs745713003 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715890 | CCTCCTCAACAGTGA[A/T]ATCATTTGCCTTTAG | 5607 |
rs745723676 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761442 | TTTGTTTAAAAATGT[A/G]TAAGCAAATAAAGCC | 5607 |
rs745726624 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598398 | ACTCTTGCAATCCTC[C/T]TGGTTATCTGAAGGA | 5607 |
rs745739742 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749382 | GGGGCTTGGGTTTGC[C/T]TACTAGCAATGTTTA | 5607 |
rs745760408 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773180 | GCTGCAAAAGATCAA[A/G]TTAATGTGAATCTTT | 5607 |
rs745766728 | snp | C/T | 3.31785e-05 | 0.00407286 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600777 | TTTTGTTTAAACTTT[C/T]TATCCGCTTTTCCAA | 5607 |
rs745781419 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551152 | TTTTTTATGAAGATG[A/G]TTACTTACAGAGAAT | 5607 |
rs745782383 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763445 | TCCTTCTGATAACAT[A/G]TGACTGCTTTTTTCT | 5607 |
rs745792832 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689290 | CCCATATGTTACATA[C/G]ATAAATCATATGCTT | 5607 |
rs745808824 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681037 | CAGTAGCTTTATAGT[A/G]TATTTGGTACATTCA | 5607 |
rs745814034 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687109 | CTGCAGTAAAATTGA[-/T]TTTTTTTAATGAGAT | 5607 |
rs745815833 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734156 | AAACCGATTAATTTA[C/T]TTGCTGCATCTGAAA | 5607 |
rs745840513 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631423 | ACTGTACTTTCGGTC[C/T]TTTCTTTTCCTATGC | 5607 |
rs745860266 | in-del | -/TG | 3.31669e-05 | 0.00407215 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693503 | ATTGTTCTAACAGAC[-/TG]TTTTGTCTCATAGCT | 5607 |
rs745879721 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67605285 | GTCTGGATCTCCTGA[C/T]GTCATGATCCACCTG | 5607 |
rs745898842 | snp | C/T | 3.29565e-05 | 0.00405921 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550104 | CTGGCTTGTATACTT[C/T]CTTGACTATTCCTTT | 5607 |
rs745899431 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678179 | AAATAACTAGATAGA[C/T]ATATTGTTTTTTTTC | 5607 |
rs745899786 | in-del | -/AGAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736190 | AGTGTAGCAGGGACC[-/AGAT]AAAGAAATTGGGTTT | 5607 |
rs745915084 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628367 | CACCTGTAATCCCAG[C/T]TACTCGGGAGGCTGA | 5607 |
rs745936819 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770504 | CATTGTCCTCAAAGC[A/G]GGAGACAAAACCAAC | 5607 |
rs745939123 | snp | C/T | 1.65737e-05 | 0.00287864 | stop-gained | MAP2K5 | GRCh38.p7 | 15:67769659 | GTACATTTCATCACT[C/T]AGTGGTGAGCCCGTT | 5607 |
rs745942525 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803676 | GCAGGGCTGATGGGA[A/G]GAGGGGGAGTCAGTG | 5607 |
rs745948248 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581984 | TGTTGTACTTGAAGA[G/T]TAAGCACCAAAACAG | 5607 |
rs745952968 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780872 | AGGAGGTGCTGACCA[G/T]GTGGTGATCAGCAGC | 5607 |
rs745954133 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757784 | TAAATGGGTATTTAC[A/G]ATATGGTATTTAATG | 5607 |
rs745982414 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800179 | AAATCTGTGCATCCT[C/G]CCATAAATTATTTAA | 5607 |
rs745986910 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566958 | TGACAATAGGTTGTT[G/T]TGTGCTGTTAAATAA | 5607 |
rs745995366 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67772719 | TAGTATGCGAAAACA[A/G]CCAAAAGAAAGGCCA | 5607 |
rs746031433 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723516 | CATAATAAACGTCCC[G/T]CAAGAGAGTCTTCAG | 5607 |
rs746032417 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737658 | GGGTCCCAGAGACCA[C/T]GAGGAGCTAGGAAAG | 5607 |
rs746033339 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783579 | TTCTGTTAGTGCACT[C/T]GTCACGCTTTGTGGC | 5607 |
rs746035248 | in-del | -/AACTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603086 | TGGTGAAATACACAT[-/AACTC]AACTCAAGTTAACAT | 5607 |
rs746037630 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593928 | GTCAAGAAGACAAAG[C/G]CAGGTCCTCATGCCT | 5607 |
rs746042446 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546290 | GAAGAATCCCCTCAT[C/T]TAATTCAGACTCATT | 5607 |
rs746048227 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769123 | AAAAAAAAAAAATTG[A/G]TCCAAATTATTCTGT | 5607 |
rs746054025 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561418 | ATTCTATATCTAAAG[C/T]GAATGAAAGAATCTT | 5607 |
rs746058177 | snp | G/T | 6.61397e-05 | 0.00575026 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658646 | AGTGTTAGGAAATTT[G/T]AGTGATTTAATCCTT | 5607 |
rs746061287 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680893 | TGCTACCCTAGAAGA[A/G]GCCTGCCTTCAGGTG | 5607 |
rs746088138 | snp | C/T | 1.65778e-05 | 0.002879 | synonymous-codon, intron-variant | MAP2K5 | GRCh38.p7 | 15:67664611 | GGTTGTTAAAGGCCT[C/T]ACTTATTTGTGGAGT | 5607 |
rs746096036 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547792 | CTTTAGGTTAGTTAG[A/G]TACATGTTATATTGT | 5607 |
rs746098141 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724633 | TTTTACCTCCTCCCA[A/G]TAGAACTTGATAAAA | 5607 |
rs746110653 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677125 | TAAAACATCTGGGCT[A/G]TTTTCTTTGTGAACT | 5607 |
rs746111890 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586843 | TTCTTTCTTTACTTA[C/T]AGGTGAATACTCGGG | 5607 |
rs746127253 | snp | C/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541168 | GAATTTCTACCTAAG[C/G]TATTGATTTACAGTA | 5607 |
rs746140431 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574924 | GTGGTTAAATACGGG[G/T]GAGAAGAGAAGAGAG | 5607 |
rs746175782 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805175 | CGAGTTTCCTCCTCC[A/T]CCTCGCAGCTCTGAC | 5607 |
rs746236679 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622913 | ACCATCCTGGCTAAC[A/G]CAGTGAAAGCCCATC | 5607 |
rs746267270 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805841 | TCACCTCTGACTGTG[A/G]CCTGGTAACCCTGGG | 5607 |
rs746286723 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589195 | GGTCACCGTGAACAT[G/T]CAGATGAATGAAATA | 5607 |
rs746299207 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719406 | TCATAATCAACAAAT[G/T]CTTATTGTCAACCTA | 5607 |
rs746308948 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727885 | CCTGCATGCAAATCT[A/G]TAACTAGACAAATAT | 5607 |
rs746315256 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795646 | ATGGTCATTTGGTTT[C/T]TCCCCCCAGTGTTCT | 5607 |
rs746353876 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624151 | GAGACCATCCTGGCT[A/G]ACACAGTGAAACCCC | 5607 |
rs746359621 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697941 | GCAATGTGCTTGTAG[A/G]AGACTTGAAAAGTCA | 5607 |
rs746368124 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665081 | AAGATGGGGTCTTGC[G/T]CTGTTGGCCAGGTTG | 5607 |
rs746373932 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699754 | TCAGATGCATACAGA[C/T]TTAAGATCACACATT | 5607 |
rs746375947 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698632 | CTATGATTAACTGAA[A/G]TTTTAAAATGAAAAA | 5607 |
rs746376001 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683583 | CTTGGCCAACATGGC[A/G]AAACCCCATCACTAC | 5607 |
rs746383515 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591601 | GTCTCAATCTCCTGA[C/T]CTCGTGATCCACCTG | 5607 |
rs746387396 | snp | A/T | 1.65042e-05 | 0.0028726 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748183 | CATAATGTGTCCAAG[A/T]GAGTCATTTTGATTA | 5607 |
rs746390067 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556814 | TGCCTCGGCCTCCCA[A/C]AGTGCTGGCATTACA | 5607 |
rs746409299 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593966 | AATATCACCTGTAAC[A/G]TTGTGGCCTAATAGA | 5607 |
rs746417967 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788215 | CATTATTTACTTAAA[C/T]AATGTATAGCTCTGG | 5607 |
rs746452768 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649588 | TTTGTTAAAGACTGT[C/T]TTTCCCATTGAATTT | 5607 |
rs746475268 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567567 | GATGGGGTTTCACCT[G/T]GTTAGCCGGGATGGT | 5607 |
rs746477144 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786860 | AATAAATGGTAACCA[-/T]TTTTTATCGTCATTG | 5607 |
rs746483565 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681202 | TCAAGATATCAGATA[C/T]CAGGATATCATATAC | 5607 |
rs746499772 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742976 | TGCTCCAGCTGTTGT[A/G]TTTTGTGTGAAAATG | 5607 |
rs746503776 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746563 | TGTTACTGAAATTCT[C/T]AACCACTTCCGGGTG | 5607 |
rs746518904 | snp | G/T | 2.11151e-05 | 0.00324917 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806909 | GGCCTTGCCTGGGGA[G/T]CCCCATGTGTGGCCC | 5607 |
rs746530838 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760726 | GAGGCCTGTGAATAG[C/T]GGTCTGTGAATGGGC | 5607 |
rs746548739 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802901 | GGGACCAGCCGCAGG[A/G]GCTGGAGACTGCAAG | 5607 |
rs746572036 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585784 | TTTTCAATCATTTCT[C/T]TCTGCTAATTTTGGT | 5607 |
rs746588236 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728943 | CTTTACTCAATGAAA[C/T]GTCTCTTTCGTATTC | 5607 |
rs746603290 | snp | A/G | 3.31126e-05 | 0.00406881 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703303 | TCCTGAGTAGCATCC[A/G]TCCACTCACAGGCTC | 5607 |
rs746615590 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683128 | CTGGGCAACAAGAGC[-/A]AAAAACTCTGTCTCA | 5607 |
rs746617993 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579838 | TTTCCTAAACATATC[A/G]TATTTAAATAATATG | 5607 |
rs746618910 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787449 | AATTTCAGGAACTAT[A/G]TTTGACTTCTCTAAA | 5607 |
rs746622141 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564599 | GAATAGGAAAAGTCA[A/G]TTTCCCATTGACTTC | 5607 |
rs746624609 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755118 | TAACTAGGATTACAG[C/G]TGTGCACCACCACGC | 5607 |
rs746637699 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658674 | CTTCTAATCAAGCTC[A/G]TTCTTCTTATATTCT | 5607 |
rs746641365 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675708 | ATGTAAACAACAAAA[A/G]AAGAATATATCATCT | 5607 |
rs746642190 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689898 | TGGTAGCTTAAGAAT[G/T]GTTTAGGGCAAACTT | 5607 |
rs746656167 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551476 | TAACTGGGACTACAC[A/G]CATGCACCACTATGC | 5607 |
rs746688136 | snp | G/T | 3.30497e-05 | 0.00406494 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703443 | ACGCTTCTGTGCATA[G/T]CTGTACTAATATATT | 5607 |
rs746705618 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644950 | GTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 5607 |
rs746731255 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660048 | AGTAAGAGCTACTCT[A/G]AAGGATTGTTTATAT | 5607 |
rs746739437 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653911 | ATTTTCCATTTTTCT[A/G]TGATAGAAATCTCTT | 5607 |
rs746768287 | in-del | -/AG | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720386 | CACACAAGGAAAAAA[-/AG]AAAATGATGTAAGTG | 5607 |
rs746781376 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750633 | GTGCCTAGAATCTAC[C/T]AGTTTCTCGGGTAAC | 5607 |
rs746835043 | in-del | -/AGA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733490 | TATTGCAGTATATGG[-/AGA]AGATCACTTTTATTG | 5607 |
rs746842238 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657005 | GACGTTTATCTCTAA[C/T]GGACATGAAAAGGAC | 5607 |
rs746854159 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765515 | AGGGTAGATTAATGA[C/T]ACAGATTATTCTAAA | 5607 |
rs746867911 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703640 | AGACCTGCCTGGAGC[A/G]CTTGTTAAAAATACA | 5607 |
rs746882594 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586539 | TGGGTATATTCTTAA[C/T]GTACTTTTTGAACAT | 5607 |
rs746890817 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730187 | TAAGCTGAAGATTGG[A/G]AAAGGATACTTTATA | 5607 |
rs746892344 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67630903 | AGCATATCATGTCCC[A/G]AGTGGGAAAATATTA | 5607 |
rs746914878 | snp | A/T | 1.6666e-05 | 0.00288664 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772760 | AATTGATGGTAAGTG[A/T]ATGTTTTTAGTTACA | 5607 |
rs746922869 | snp | C/G | 1.64808e-05 | 0.00287057 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550115 | ACTTTCTTGACTATT[C/G]CTTTCTGCAGTCATT | 5607 |
rs746926291 | snp | C/T | 0.000100065 | 0.00707266 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806660 | GGGCCACCCGTTCAT[C/T]GTGCAGTTCAATGAT | 5607 |
rs746931115 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660669 | TTGCATGCTTTCTAT[A/G]CAAATATTATGTCAT | 5607 |
rs746931198 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666788 | AGAAGATATCTGTTG[A/G]GGACACAGTAGGAAC | 5607 |
rs746952036 | snp | C/T | 0.000119653 | 0.00773383 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658785 | GACCAGCCCACCCAA[C/T]ATCACAACATAGTCA | 5607 |
rs746969262 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791172 | CTGTGAATTGGCTTA[A/G]TGTCAGCAGTTAGCT | 5607 |
rs746975132 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668395 | CCCACCAAATTAACT[A/G]CTGTGGAAAAGTTGT | 5607 |
rs746976568 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706547 | GGATGGTAAGGAGCC[A/G]GGTGTTACAGCAGGA | 5607 |
rs746993789 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665178 | GAGCCACCGCGCCTG[A/G]CCAAAAGTAAAACTT | 5607 |
rs746994072 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804267 | GTCCACAGTGCACAG[C/T]CTAGGACGCTGGGTC | 5607 |
rs747004321 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619847 | GAGGCAGGAGGATCA[C/T]TTGAGGCCAGGAGTT | 5607 |
rs747008190 | in-del | -/ATA | 1.88156e-05 | 0.00306715 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593005 | TATTAAGATTTTCAC[-/ATA]ATAATAACATATTAC | 5607 |
rs747042162 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801183 | GGAATCCTAAAGGGA[A/G]ATGCATAGAGCCTTC | 5607 |
rs747066015 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617125 | CAAGAGGCAAAAAAG[A/G]GGTATTTCCGTGCTC | 5607 |
rs747070214 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758882 | ACTGAACATTTTGGC[A/G]TCAAAGGAAGAGGTT | 5607 |
rs747072307 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746578 | TAACCACTTCCGGGT[A/G]GTGGTTACAGCTCCG | 5607 |
rs747080098 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783691 | CTAGCCCAGTCTCCA[A/G]CCTGAGTAGAATGCT | 5607 |
rs747099608 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568863 | TACTAAAAATTAGCC[A/G]GGCGTGGTGGCATGC | 5607 |
rs747101135 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579809 | GTCAGCAAACAATAG[C/T]AATCAAGGAGGGATT | 5607 |
rs747104581 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651122 | ACTTGAGAGGCTGAG[G/T]CAGGAGAATCACTTG | 5607 |
rs747105904 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756656 | ATTTATCTTATAAAA[C/G]TAAGTTTGTCCCCTT | 5607 |
rs747118377 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683487 | GAAAGGGAGGCGGGG[C/T]GTGGTGGCTCATGCC | 5607 |
rs747131822 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557317 | GAAACATGCATTTTA[A/G]GTCCATGTAGACAAA | 5607 |
rs747135437 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714651 | ACTGATATTTTCTCT[A/T]CTTCTTTTTAAATAT | 5607 |
rs747152165 | snp | A/C/G | 4.97132e-05 | 0.00498543 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664657 | AGAGGTATGTGCTGG[A/C/G]CTTATAAGCTTGGAT | 5607 |
rs747156998 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726286 | GTTTATTCCTGTTAC[A/G]TGGCTATTGTTCATA | 5607 |
rs747170390 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566187 | TTTTGGTCTTGTTTT[-/G]TTTTTGAGATGAAGT | 5607 |
rs747171862 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725795 | GTTCACCCACCACAG[C/T]AGACCATAGTAATTC | 5607 |
rs747186889 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582978 | TCATTCTCACTGTTC[A/T]TCGCATTATGCTTCT | 5607 |
rs747196827 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757813 | TGATGTTTGTAGCCA[C/T]ATAAATTCTATAATT | 5607 |
rs747205255 | snp | C/T | 3.29511e-05 | 0.00405887 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586942 | AGTAAAGTGTGCCCT[C/T]GATGTGATTTATCTA | 5607 |
rs747221813 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678280 | GCTAGGAGTGGAGAC[C/T]GGCTAATGTGCCCTC | 5607 |
rs747230230 | snp | C/T | 0.000185787 | 0.00963634 | synonymous-codon, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549207 | TCACTTTCCCCAGAG[C/T]GTAGGTGTTCTATGC | 5607 |
rs747251276 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800219 | TCTGAAGTTTTCTCC[A/G]GGGATTAGATTGGTA | 5607 |
rs747256458 | snp | A/G | 0.00130855 | 0.0255453 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592950 | GTCTTCTGCTGAACT[A/G]AAAAAAATACTAGCC | 5607 |
rs747267552 | snp | A/G | 3.30983e-05 | 0.00406793 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543292 | TCCTAACCAGCGGCC[A/G]GTGGGTTTCCCATAC | 5607 |
rs747268067 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713382 | GAATTGTGATCTTCT[A/G]TACGTATAAGTAAAC | 5607 |
rs747273525 | snp | A/T | | | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806814 | ACCCACCCGTCGCCC[A/T]TCTCCGTATGCTGCC | 5607 |
rs747276606 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629178 | AAGAGGAGAGCTAGA[A/G]AAGTGACGGGGAAGC | 5607 |
rs747276704 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546436 | CATAACTGAGTGTCT[C/T]GGACCTGAAGTCAGC | 5607 |
rs747295464 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762991 | CATGTAATTTGTCAC[-/G]CCTGGCAGCCCAGAG | 5607 |
rs747309489 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795483 | TAGGACTTTTTTACA[C/T]CAAATTATTTAGAAG | 5607 |
rs747310014 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663383 | GTCTTTCCTTACTTT[C/G]ATATTTTGGAAGAGT | 5607 |
rs747310931 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626401 | GTGTGGTGGTGGGCT[C/T]CTGTAATCCCAGCTC | 5607 |
rs747331816 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674550 | TCTCCAGCTCTGACA[C/T]TATCCACACAAATGA | 5607 |
rs747343228 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754220 | TGGAACTGGTTTGTT[A/G]CTTTAAAAGGGTGAA | 5607 |
rs747361916 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639057 | AATACCATTCTGGAC[A/G]TAGGAGTGGGATAAA | 5607 |
rs747366035 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765864 | CCAGTTGAAGTTAAC[A/G]TACATTAAGCATTCT | 5607 |
rs747379660 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623940 | TTAGTCTTATCTCAT[C/T]GGATCCTCACAACTC | 5607 |
rs747380114 | snp | A/C/G | 3.29882e-05 | 0.00406118 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748214 | TGACATGCTAATTAC[A/C/G]TATTGCCTTTTTTCA | 5607 |
rs747386570 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767397 | TTGAACGACATTAAG[A/G]TAGCAGGCTTTTATT | 5607 |
rs747401345 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557060 | TTCTGGGTCCTACAT[-/A]ATGCTGTAAGAGCTT | 5607 |
rs747415063 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707019 | CTCCCAGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 5607 |
rs747416632 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589315 | TAGCATAATGAATGA[A/G]ACAGTATTTTCCTCT | 5607 |
rs747425528 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578340 | TGCTCCGTAGGCAGT[A/G]GCCTGAGTTTCTAGG | 5607 |
rs747431161 | snp | A/C | 0.000104805 | 0.00723821 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646206 | ATTAGAAGATTAAAA[A/C]ATATTAATACCTTTC | 5607 |
rs747436470 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611061 | TGGAAGATATGTATT[G/T]TGTGAGGTTCTCAAA | 5607 |
rs747481306 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733916 | GTGTGTTCAACCCCT[A/G]TATACTACATATCAA | 5607 |
rs747492395 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734938 | TTTTTTTCTAAACAG[A/T]TGTCTAGCCTATATG | 5607 |
rs747506902 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565568 | ATAATTTGGGTTTAT[A/G]TAATACCTTAGTTGT | 5607 |
rs747520299 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543256 | TGCCCGTCACTCCCC[A/T]TGTCACCTCTTGGAG | 5607 |
rs747550737 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701107 | TGTATTCTGGGTGAA[A/G]TACTTGGTACCTGTT | 5607 |
rs747562689 | snp | G/T | 1.78096e-05 | 0.00298404 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646363 | TTGCAGGTTTATAAC[G/T]ACTTTTGTCTTATTT | 5607 |
rs747591656 | in-del | -/ACACACACACAC | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547079 | AAAAAAGAAGAAAAC[-/ACACACACACAC]ACACACACACACACA | 5607 |
rs747600992 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664781 | AAGATGGCTGCTCTA[C/T]AAATGTTATTTTTCT | 5607 |
rs747603177 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804328 | TGTCAGGCAACCACC[C/G]TAAACCAATCAACAG | 5607 |
rs747610044 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806013 | AACCAGAGGCAGGCC[A/T]CAGGGCAACAGGGCC | 5607 |
rs747665486 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763030 | GAGCCAGTGTGGAAA[C/T]TGAATCATCTTTCAC | 5607 |
rs747685006 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761735 | ATCTTAACTCTTTAT[C/T]TATGAAAAGATCAAT | 5607 |
rs747685266 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601207 | GTTGTATTTTCTTCT[C/G]TCCTCACCCTACTCC | 5607 |
rs747693422 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620931 | AAGTAAATGAATTAG[A/G]TGGTAGAAATAAATC | 5607 |
rs747701732 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587523 | CTCCTTGCCAAATGG[C/T]CATCAAATCTCTTAC | 5607 |
rs747702534 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566707 | ATTACTTTTTCCCCC[C/T]CTTGGATGCAGGCAT | 5607 |
rs747708019 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573229 | GGTTCAAATGCCTCT[A/G]ACAACATTGCTATAA | 5607 |
rs747726817 | snp | C/T | 1.67475e-05 | 0.00289369 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630967 | AATTCTTGATGTTCA[C/T]CTCTTTCCTTTCCTC | 5607 |
rs747736148 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717719 | GAAGATCCAAGATGA[C/T]TTCATATGCGTGTAT | 5607 |
rs747753328 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696249 | CTCAGGCCAAATTCA[A/G]TTTACTGGAACAATG | 5607 |
rs747756174 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552864 | GTTTCCAGAGTGTAT[A/G]TTCTCAACCACTGTA | 5607 |
rs747779391 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67661101 | GGACCTCTGTTGACC[C/T]CTGTGATATGTTATT | 5607 |
rs747779851 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550128 | TTCCTTTCTGCAGTC[A/G]TTTTTTAAAGGGTTT | 5607 |
rs747813499 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682239 | TTTTTTTTTTTTAAG[A/G]TAGAGTCTTGTTCTA | 5607 |
rs747831837 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660890 | AAAAAAAAATAGAGG[C/G]AGGAGTGGAAGAAAG | 5607 |
rs747846320 | in-del | -/TTC/TTCTTTCTTTCTTTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575917 | TCTTTCTTTCTTTCT[-/TTC/TTCTTTCTTTCTTTC]TTTTTTTTTTTTTTT | 5607 |
rs747850597 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697484 | GACTAAATTCTTAAT[C/T]GCTGTGCCTCTCATT | 5607 |
rs747860106 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730416 | TAAAACTGTGACTGG[C/T]TTGGTTTCTTTGAAT | 5607 |
rs747865280 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647651 | AGCACTTTGGGAGGC[C/T]GAGGCAAGCGGAGTT | 5607 |
rs747892096 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690909 | GCTTGGAAGGGATAC[A/G]TTTAAAGATGTTTTA | 5607 |
rs747892885 | snp | A/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663417 | TTGCCCAGTACTTTG[A/T]TTATATATTTTTACC | 5607 |
rs747917791 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655926 | TCTTTTCTTTTCATC[A/G]TTACACTGGATAATT | 5607 |
rs747919454 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594087 | GAAGTTGATCTGCTT[C/T]TGACATCTGATTGCC | 5607 |
rs747921651 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738055 | TGAGATTTCGCCATG[C/T]TGGCCAGGCTGGTCT | 5607 |
rs747962377 | snp | G/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548410 | CTGGAATTTCAAAGT[G/T]TATTACGAAGTAAGC | 5607 |
rs747989062 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751677 | TGGCAGCCTGTTGAC[A/G]GAGTGTGGTGAATAT | 5607 |
rs748022409 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724806 | GACTGCTTTCAGTGC[C/G]AGCCTAATAGTGCAC | 5607 |
rs748026087 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734839 | GGTCTTTAATCAAGG[-/A]AAAAATAGCAATGAG | 5607 |
rs748029666 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742686 | ACAGACCTCATACCA[C/T]CAGGAAAAAGATTTT | 5607 |
rs748031548 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711009 | TCTCCAGCTGAAGGT[-/A]ATATCTTCTTCTTCT | 5607 |
rs748040715 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653652 | CTTTGATTTTCTCTA[-/T]TTTTTTTTTCTATTC | 5607 |
rs748041362 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563339 | GAGGAAATGAAGGCA[A/G]TGCTGTCATATGTAA | 5607 |
rs748050288 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692472 | GCCTTTTCTGGTCCC[C/T]TTTTAGACGTGAAGC | 5607 |
rs748052186 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561578 | TGTGATCTTGATGAT[A/G]CCGATTCACACTGAG | 5607 |
rs748068104 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703949 | TGTATGTGGGTTAAG[A/G]GGTGGTGTGATATGA | 5607 |
rs748075195 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669899 | TGCTTTGAAAAATAG[C/T]TTGACAATTTCTTGC | 5607 |
rs748077088 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655202 | TTAAAATTATGCCAT[-/TG]TCTCTTAAGTCATAG | 5607 |
rs748078229 | snp | C/T | 3.31439e-05 | 0.00407073 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664660 | GGTATGTGCTGGGCT[C/T]ATAAGCTTGGATTTA | 5607 |
rs748091403 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622366 | ATTGTGCATAAGGGA[C/G]ACTGGAAGAAGCAGA | 5607 |
rs748113713 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652211 | TTCTGAGGTTTTCGG[G/T]GTGTGTCATTAGTGC | 5607 |
rs748138320 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582501 | AGCTCTGCCATAGAA[A/C]ACCCTAATTGCAGTA | 5607 |
rs748174976 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778821 | GCCCTGAGCGCAAAT[A/G]TGAAGAAAGGTGCAT | 5607 |
rs748191904 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702281 | TATGCATGAAAAACA[A/C]TAAAACAAGGCCTGG | 5607 |
rs748193656 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766221 | AGCAGAACTCTAAAG[C/T]TGATTTGAGACTAGA | 5607 |
rs748194876 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604353 | TTTTCCTTGTTGCCT[C/T]ATTTCCTAAAGTGCT | 5607 |
rs748195442 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591148 | TCAGGAGTTTGAGAC[C/G]AGCCTGGCCAACATG | 5607 |
rs748205166 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733995 | TAACCAAGGAAATAC[A/G]TTTTGCAAATGCTTT | 5607 |
rs748226794 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760537 | ACTAACCAAAATATT[A/G]ACATAAACATCCCCA | 5607 |
rs748238643 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559395 | TAGGCCATTGTGACC[G/T]CCCCTTACCTGAGGC | 5607 |
rs748314208 | in-del | -/TC | 1.64751e-05 | 0.00287007 | frameshift-variant, intron-variant | MAP2K5 | GRCh38.p7 | 15:67727933 | TGCTCTTGGGAGGTT[-/TC]CATATCCTCAGGTAA | 5607 |
rs748337007 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570752 | AACTAACAAATTAAC[A/T]ATGGACTGCAAATAG | 5607 |
rs748340046 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67680723 | CTATTATCTACTTGG[A/G]CTGTCACTGCTGCAA | 5607 |
rs748345154 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585540 | CTCTTTTCAAAGTAG[A/T]TTAAGTGATAGCAGA | 5607 |
rs748346317 | snp | C/G | 1.65247e-05 | 0.00287438 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543309 | TGGGTTTCCCATACC[C/G]CAGGATGTGAGCCTC | 5607 |
rs748348353 | snp | A/G | 1.70159e-05 | 0.00291679 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600650 | TTCCATCCACAGCAT[A/G]ACACCCTTTTTGTTT | 5607 |
rs748371732 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714853 | TAAGTATAATGCAAA[C/T]ATTTCAAAATCCGAA | 5607 |
rs748372367 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665366 | AAGTGAGAAAGAGAC[G/T]ATAACAAAGCAACTT | 5607 |
rs748386374 | snp | G/T | 1.65121e-05 | 0.00287329 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748621 | GGCATCGTCTTATGT[G/T]CTTTCACTCCTAAAG | 5607 |
rs748399659 | snp | G/T | 6.58957e-05 | 0.00573964 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543414 | AAGATCCCAAATAGT[G/T]GCGCGGTGGACTGGA | 5607 |
rs748446450 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785137 | TTCAGTAGAGACGGG[G/T]TTTCCCCATGTTGCC | 5607 |
rs748458294 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618226 | CTGAACACTTTGTGC[A/G]AAGTACTTCGCTTGG | 5607 |
rs748481068 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800120 | ATTAATATTATCAGG[C/G]TGCCCACTATCCTGC | 5607 |
rs748483964 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801020 | TTTAAAACTGTAGCT[A/G]AAAATTTTCTTAACA | 5607 |
rs748491885 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613785 | CTTGAGTTTTTAATG[A/G]AAACGGGTTAATATT | 5607 |
rs748510357 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710424 | GAAAAATGTCTCAAC[A/G]TAGGTAAAGAACATA | 5607 |
rs748514573 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714413 | CTACCCAGCTGCCAG[-/G]GAAAAAAAAAAAAAA | 5607 |
rs748527863 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580212 | AGCATAAAAGGTATG[C/T]TTGTTTGAAACTAGG | 5607 |
rs748532348 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786233 | AAATTATATGTATGT[C/T]GGATGTTTGCAATTG | 5607 |
rs748539105 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693382 | TTTTATTGCCTTTGT[-/A]AGATAAATTTGTTCC | 5607 |
rs748573464 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676278 | TTGGTAGAGGAGTTT[A/G]TGGCATTGATTGTAT | 5607 |
rs748575457 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580834 | AAGAGGTAATGTTGA[A/G]CAAATTCTAATCAAC | 5607 |
rs748579986 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544613 | ATTCATTTGAGATAG[A/T]CAGGGTGCCTTGTGC | 5607 |
rs748584528 | snp | A/G | 3.30978e-05 | 0.0040679 | missense | MAP2K5 | GRCh38.p7 | 15:67769611 | TCACAGGATTCGCCC[A/G]TCCTTCCAGTTGGAG | 5607 |
rs748590500 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743162 | TTTTTGCTTTTCAAA[A/G]CTGGTCACTCCTGAA | 5607 |
rs748605403 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673743 | AGCTTTGTAACAATC[-/TG]TTTTTTTGCAGAGAT | 5607 |
rs748635321 | snp | A/G | 1.89109e-05 | 0.00307491 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646511 | TAAAATGATTTTTAG[A/G]GTATATAGTGCTTTA | 5607 |
rs748654288 | snp | C/T | | | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806963 | CTTCTGGTTTGAAGG[C/T]GCTGACACTGGCAGA | 5607 |
rs748658546 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688154 | GACACAGAGCCACAG[C/T]GCAAGAGCATACCTG | 5607 |
rs748662021 | in-del | -/CA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628261 | CTGAGGTGGGCAGAT[-/CA]CGAGGTCAGGGATTT | 5607 |
rs748703292 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746073 | TTCTTTTAATGAAGA[A/G]CAAGCATAAATAGTA | 5607 |
rs748708915 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640184 | AGCATTACACATAAC[G/T]AGTAAGTGTTCAATA | 5607 |
rs748713473 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585911 | AGCCTCCTGGGGAAC[A/G]GAACATACATGGCCT | 5607 |
rs748715218 | in-del | -/TTAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633900 | ATTCTTAGAAGTGTG[-/TTAT]TTAGTTTCCAAATAT | 5607 |
rs748719990 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545922 | GGACTTGGGTCTTCT[A/G]TTTCTTGAGCATCTC | 5607 |
rs748724049 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708529 | AGACGTGGTCTTGAT[A/G]TGTTGCCCAGTGTTG | 5607 |
rs748729351 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625967 | AATCATTTTCTTATC[A/G]CTGCTGCTGGTCTCA | 5607 |
rs748732721 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590945 | TGTGTCTGTGTTCTC[A/G]GGGAGCTCCCAGACT | 5607 |
rs748740286 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568927 | GGAGAATTGCTTGAA[-/C]CCCGGGAGGCAGAGG | 5607 |
rs748746464 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675797 | AGTTTTTCTCTCTCC[C/T]ATGCTTCTGTGGTAG | 5607 |
rs748746614 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797044 | GACAGTGTTTCCTGC[C/T]AAAATCAGAACTCTT | 5607 |
rs748760828 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793870 | TGAGAGGACCAAAGA[A/G]TCATGAATGTGCCAG | 5607 |
rs748767757 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794968 | AACCTCTGACGCCCC[C/T]GCGGTGGGTGATGTT | 5607 |
rs748770407 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655096 | AGTATACAAAAACTT[C/T]GCTTCTGTATAGCTC | 5607 |
rs748771278 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764433 | TGAACTCGCGTCTGC[C/T]AGCCAAACTGAACCA | 5607 |
rs748773236 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751822 | TTTCACTGAATTTTA[C/T]CAACCATTTTGCCAG | 5607 |
rs748793411 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671139 | TGATCACTCAGATTT[C/T]TTCAAGAGCTAAGGT | 5607 |
rs748800684 | snp | A/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720138 | TACTATGGCCTAGTT[A/T]AAATTGTATATTCCA | 5607 |
rs748827776 | in-del | -/TTA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635110 | ATCCCAGCCTTTGTT[-/TTA]TTATCATCCATTTTA | 5607 |
rs748834601 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561793 | TAGGCTAATTGTGAA[A/G]GAACACAAGCTTCCT | 5607 |
rs748837516 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718240 | TTTTCTCAAATACCC[A/G]CAGCTGCATGATTTC | 5607 |
rs748853318 | snp | A/G | 0.000113604 | 0.00753586 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646186 | TAGTGATTATAACTA[A/G]TATAATTAGAAGATT | 5607 |
rs748857686 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804491 | ATCTCCACCGGAGCT[G/T]AGTATGGCTGCAGCT | 5607 |
rs748859021 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609751 | TGTAGAAGAGGTGCT[C/T]AGGAAGACCTATCTG | 5607 |
rs748862346 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795410 | TAGCTGCATCCAACA[A/G]GTATTTACATGCAGT | 5607 |
rs748864606 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660903 | GGCAGGAGTGGAAGA[A/G]AGAGCTAGGCTAAAA | 5607 |
rs748869937 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556475 | TAAATTTGTATGTGT[A/C]GTATTGTGGGTTTTT | 5607 |
rs748888311 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683452 | ACAATGAACAAAAGA[C/G]AAAAGCAAACATTTT | 5607 |
rs748904435 | snp | A/G | 2.19022e-05 | 0.00330917 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646339 | GTAAAGCATGCCTAT[A/G]GTATTGACTTGCAGG | 5607 |
rs748906365 | snp | A/G | 3.31802e-05 | 0.00407296 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563365 | TGTAAGTATACGACA[A/G]ATGAAGACTATTTTT | 5607 |
rs748927633 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663992 | TCTCTCCTTCCCTGG[C/T]TTAGCATCATTATGA | 5607 |
rs748928344 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777073 | CAATGATTGTTAAGC[C/T]CCCTTGCTTCTGTCC | 5607 |
rs748981807 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67636229 | CATCCTAACACGGTG[A/G]AACCCCATTTCTACT | 5607 |
rs748986989 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629316 | CTTGAGGACTGTATT[-/TG]TCTAATTGTATAACA | 5607 |
rs749003928 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719248 | CAGTGATACGTAAGA[C/G]GGCCTTGTCGGTTAA | 5607 |
rs749024275 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804959 | TGCTCAGGCCCCAGA[A/C]CAAACCTCTGCCATC | 5607 |
rs749031612 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805763 | GAAGCCACTTGGTGT[A/C]AGTTCCTGGGCAAGA | 5607 |
rs749034106 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644043 | TAGAGCCAGAAACTC[C/T]GCCACAAATCATAAA | 5607 |
rs749034883 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679650 | AACCATTTTACCATT[A/G]ATATATAGTATATGT | 5607 |
rs749060190 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784079 | AGAAATGGATCTAAA[C/T]ATAAAACATTTTAAA | 5607 |
rs749083156 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617196 | ATAGGATATTGTCAG[C/T]TATGCTGAAATCTGA | 5607 |
rs749107808 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801429 | CTTGGTGGGAGAGGA[A/T]GTGCTTGGTGCTCAC | 5607 |
rs749111243 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759121 | GCTCTTAAATGTGTT[A/G]TCTTAAAAAATTCAT | 5607 |
rs749120418 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740177 | TGTGGGCCAGCAATT[A/G]TATTCTATCCATCTT | 5607 |
rs749120481 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610689 | GTCTTACTAGAGTGA[A/G]ATATGTTTAGGTTCT | 5607 |
rs749139460 | snp | A/C | 3.88931e-05 | 0.00440965 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806868 | CCCTGGCTTCCCTGC[A/C]CTCGCCTTCACCTCT | 5607 |
rs749141709 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630840 | CCTTAACCATTTTGT[A/G]GGTTGTTTAGTGATC | 5607 |
rs749143178 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67692514 | CTAGTAAACACAAGA[A/G]GACAGGTTAAGCTGT | 5607 |
rs749147675 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584227 | TTTAGGAAATATGAG[A/G]TTACTGGGTTTTTTG | 5607 |
rs749180482 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706674 | TTCAGAAGGAACTAT[A/G]GGATTGTAGCCCCTG | 5607 |
rs749188546 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595957 | GAGTTTGGCCTTTGC[A/G]TCTCTAAAGTTATTT | 5607 |
rs749196875 | snp | C/T | 0.000628504 | 0.017716 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600672 | TTTTTGTTTTTCTTT[C/T]TTTCTTGTGGAGATG | 5607 |
rs749208647 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785476 | TAGGGAATACAGAGG[G/T]CTATCAGACACTAAT | 5607 |
rs749216500 | snp | A/C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656529 | AGATGGGGTTTTGCC[A/C/G]TGTCTCCTAGGCTGG | 5607 |
rs749224012 | in-del | -/AA | 3.29821e-05 | 0.00406078 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585845 | TTTGAGCAAATTTGT[-/AA]ATGGCCCTGATGTGT | 5607 |
rs749228133 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549557 | GTCTAAGTTTATGTT[C/T]ATTAGATTAATTTTT | 5607 |
rs749236355 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678371 | GGGAAAAAGTTGAAG[A/G]GAAGTTTATTTCTGC | 5607 |
rs749268871 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640459 | TGTGTGACTTCAAGC[A/T]TGTCACTTGAACCTC | 5607 |
rs749276477 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741669 | GGGTGGGGGAGTGTT[G/T]TTGGAGTATCCTTAG | 5607 |
rs749282096 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783632 | TAAAAGAGACCACAA[A/C]CCCTCGAGGAAGAGA | 5607 |
rs749287871 | in-del | -/TTTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673844 | TCTGGAGGATCAGTT[-/TTTG]TTTGTTTGTTTATTT | 5607 |
rs749330794 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689714 | GTCTTTTGGAATATA[C/G]TTTAGCAGTTTTGTT | 5607 |
rs749332089 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627338 | AAAGGTTAAATAATT[A/C]TTTGGTAAAGTAAAC | 5607 |
rs749333248 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675876 | AAATTACCCTCTTCC[A/C]TTCTGAAAATGAGTA | 5607 |
rs749370579 | snp | A/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592772 | CTTTTGCATTTGGCC[A/G/T]GTTACTTTTGAAAAA | 5607 |
rs749387631 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768816 | ATAAACACAGTGGCG[C/T]TCTCTGTCATTCTTG | 5607 |
rs749393906 | in-del | -/ATG | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721951 | AATTTGCAGTGTATT[-/ATG]ATATCATACAAGTTA | 5607 |
rs749396399 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543434 | GGTGGACTGGACAGT[A/G]CACTCCGGGCCGCAG | 5607 |
rs749407245 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797916 | TCGAACTCCTGAGCT[C/T]AGGTGATCCACCCGC | 5607 |
rs749410646 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750444 | CGGAAAGGAAGGATT[G/T]GTGGGGTCCTGTACT | 5607 |
rs749416262 | in-del | -/A | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547699 | GACCTCAAGTGATCC[-/A]ACCCACTTCGGCCCC | 5607 |
rs749419130 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701963 | ATTTAATGCTAACCC[A/G]TAGCTCTAGACTTTG | 5607 |
rs749422004 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580397 | GTGAAGCTTCTTCAT[G/T]TTGCTTTGCAAAATC | 5607 |
rs749467691 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602501 | CCAAACCTTTAGTTT[G/T]ATATTAATTGAAGGT | 5607 |
rs749472424 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572835 | TCCTGAGTAGCTGGG[A/G]CTACAGGCACCTGCT | 5607 |
rs749489821 | snp | A/G | 3.30825e-05 | 0.00406696 | missense | MAP2K5 | GRCh38.p7 | 15:67769620 | TCGCCCGTCCTTCCA[A/G]TTGGAGAGTTCTCGG | 5607 |
rs749491245 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652283 | TTAACCTTATTAGCC[A/G]TGATATTAGTCCATC | 5607 |
rs749510499 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702455 | AAGTTATGATCTCAG[C/T]CTTGCCATGATTAGC | 5607 |
rs749523812 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688453 | GGTGCATATAGTCTG[A/G]CAAAAATGTTTCCTT | 5607 |
rs749526630 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544835 | ATGTTACTGACTGCC[C/T]AGGCCATGCAGATTT | 5607 |
rs749536047 | snp | A/G | 1.65315e-05 | 0.00287498 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658520 | TGTTCTGGTAATTTC[A/G]TTTGTAGTAACATGG | 5607 |
rs749575583 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67604618 | GTATCTAGGTTGGGC[A/G]GGGTGCGGTGGCTCA | 5607 |
rs749581128 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653768 | CTGTTTAAGGTAGCA[A/G]GTTAGGATATTGATT | 5607 |
rs749600373 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647801 | TTGAACCTGGGAGGT[C/G]GAGGTTGCAGTGAAC | 5607 |
rs749614221 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786804 | TAAGTGAGATAAAAA[C/T]GTTAGACACTTAGCA | 5607 |
rs749616267 | in-del | -/AGGAAGCC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775578 | GAAGATATAAAGTAG[-/AGGAAGCC]AGGAAGCCACACAGA | 5607 |
rs749628874 | in-del | -/TCT | 4.96783e-05 | 0.00498364 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748551 | TAATACTTTTTCCTC[-/TCT]TCTTTTCCATTGCAG | 5607 |
rs749636881 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744628 | TATAATGTAAAAGGG[G/T]CTGGTAGCAAGATCT | 5607 |
rs749636931 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600069 | TTATGTATTATAATA[C/T]TCGACTATATGTGCA | 5607 |
rs749638021 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649349 | TCTTTTCACTTTCTT[C/T]TTTCTTTTCTTTTCC | 5607 |
rs749642897 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780781 | AAAACATTTAACAAC[A/C]AGTATAGCATGAGGA | 5607 |
rs749672105 | snp | C/G | 3.30327e-05 | 0.0040639 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658627 | GCAGTAAGTATATGG[C/G]TTCAGTGTTAGGAAA | 5607 |
rs749677444 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635009 | ATTGCTTTAGAATTC[A/G]TAACTTAACATAGTC | 5607 |
rs749711669 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553709 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 5607 |
rs749717021 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565824 | TTTGTTGCCCAGGTT[A/G]GCCTCAAACTCCTGG | 5607 |
rs749725129 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746346 | TGAAACACATTCTCT[C/T]TGATGTCAGAAATGG | 5607 |
rs749727710 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660216 | GCTCTTTGTCTGCCA[C/T]GGAAATGATCACCTC | 5607 |
rs749737341 | snp | A/C | 1.64806e-05 | 0.00287054 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585934 | CATGGCCTGAAGGTA[A/C]GAATTTCAATAATTG | 5607 |
rs749739368 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730537 | TGAAAAGCAAACATC[C/T]ACACTGCTTGAACAC | 5607 |
rs749742239 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724386 | TGGAGAACTCGTTCT[C/T]TTTTATTTATTTATT | 5607 |
rs749757295 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581762 | GGCTCCTATTTGCAC[A/T]GATAAAGTCTCCAAA | 5607 |
rs749775619 | in-del | -/TTAAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767976 | TTCTGGATGAATAGA[-/TTAAAT]TTAAAGAGGACAGAT | 5607 |
rs749846457 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786352 | GCCATAACTTTTCAT[A/G]TCTGTCCTTTATTAT | 5607 |
rs749864538 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628254 | TGGGAGGCTGAGGTG[C/G]GCAGATCACGAGGTC | 5607 |
rs749864568 | snp | A/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661392 | TGAAAGGAGGTGCAC[A/T]TGACATGTCAAGGAG | 5607 |
rs749881679 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766910 | TCTGCATCTCAGAAA[A/G]TTCTCCCTTGAGCGA | 5607 |
rs749894198 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639820 | AACACTTTGATTCAC[A/G]TATTCCTCTCTAATT | 5607 |
rs749919877 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797445 | TGATTGTGAGTTTAA[G/T]TGGATTTAGAAGCTT | 5607 |
rs749920728 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659854 | CTGAACTTCATAAAT[A/C]TTACTTCCCTCTTGT | 5607 |
rs749926844 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626552 | ACAAACAAAAAACAT[A/C]ATATAGGGGATAGGG | 5607 |
rs749934468 | snp | A/G | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807430 | GTGGCTGAGGAGGGA[A/G]TGGGCTGTTCTGAGA | 5607 |
rs749937750 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592410 | GTTCAGAGAGGATAA[A/G]TAACTTGTCCCAGAT | 5607 |
rs749971622 | snp | A/C | 1.7603e-05 | 0.00296668 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646486 | TGAGTTTTCCCTTTT[A/C]TAATACTTTTAAAAT | 5607 |
rs749978684 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653596 | CCACCACACCCAGCT[-/AAA]AAAAATTTTTTCATT | 5607 |
rs749992778 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593067 | AAACAGATAAAGAGT[C/G]TGTGAGTTTCCTGTC | 5607 |
rs749995647 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735148 | CAAATTCTTCTCCAT[A/G]TCTATTGTGTACTTA | 5607 |
rs750002715 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722860 | AGGTAATTAAGAACA[A/G]ATTTTAGAACATTTC | 5607 |
rs750032108 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734792 | ATGAAGGATTTAAGT[A/G]AATTTTTAAATATAC | 5607 |
rs750042733 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686388 | AAGGCAAGCAGATCA[C/T]GTGAGTTCAGGAGTT | 5607 |
rs750049127 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704623 | CATATTCTTCTGCTT[C/G]TTCTTAAAAGGGAAT | 5607 |
rs750056858 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558929 | ACATAGTGGGTACTT[C/T]TATTTGCTGGAAGGA | 5607 |
rs750057936 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779507 | CAGATAAATATGTGT[G/T]TGTATGTATATGTCT | 5607 |
rs750073349 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735828 | TCATAATAATAAACT[G/T]GGTGTCCAGTCTGGC | 5607 |
rs750110987 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559901 | CAAATTATTTTCTTG[C/T]TTCTTAGTACCACTA | 5607 |
rs750117666 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675683 | TAGTTATCTCAAAAT[G/T]AAAAGCTTAATGTAA | 5607 |
rs750123245 | in-del | -/CT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731878 | CTGCCCTAGGGAGGC[-/CT]CTCTTGTATAGATGA | 5607 |
rs750128775 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586866 | TACTCGGGCCGGACC[C/T]TCTCAACACAGCAGC | 5607 |
rs750131503 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721697 | CATAATTCTGTTTGC[A/G]CTGAAGAAATCCTTA | 5607 |
rs750137523 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687789 | ACCATTTGCTCAACA[A/G]ATATTGTTTCCTGTA | 5607 |
rs750141315 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566748 | TGGGCCAGTACAAGT[A/G]TACATTTTTATTAGT | 5607 |
rs750158812 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552063 | GGACTTGGGGCCTGA[-/G]GCTTGGGTTGGTGGG | 5607 |
rs750220228 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599142 | GTCCAGAATAATGAG[A/G]TTTTATTTTGTTTAT | 5607 |
rs750229805 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647280 | GTGTACAACATGCTC[G/T]AAATTAGTTATAGTA | 5607 |
rs750246088 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634143 | GTAGGTGGATGACTT[C/G]AGCTCAGGAGTACGA | 5607 |
rs750251272 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775397 | GGGGAGGCCAGGATA[A/C]GTTTCAGCTGCTGTG | 5607 |
rs750273153 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586424 | TTTCATAATTAATTA[A/T]TTGGACCTCATTTTT | 5607 |
rs750298625 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613513 | TTTTAAACACTGTAA[A/T]GCAGGATGAAACTAG | 5607 |
rs750316492 | in-del | -/GG | 6.31931e-05 | 0.00562073 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806777 | GGCACTGAAAGCCCA[-/GG]ACCAGTAACCAAGGA | 5607 |
rs750320335 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756041 | TAATGGAGAAAGCCA[C/G]CATCTCTCCCCCACA | 5607 |
rs750323076 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798165 | ACATGCTGCAGACTC[C/T]ACCTTTCAGGGGTGA | 5607 |
rs750325152 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790047 | ATAGCCAATAGCTGG[A/G]GGTAAACTACAAGAG | 5607 |
rs750335992 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581149 | CTGGATATTTATAAA[C/T]TGTGGCTCATGATGG | 5607 |
rs750356701 | snp | C/T | 3.30224e-05 | 0.00406326 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703429 | TTGTTTGCACATAGA[C/T]GCTTCTGTGCATATC | 5607 |
rs750371515 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781926 | TTTTTCCACTTAAGA[-/G]GGCTGTGCTGAAACA | 5607 |
rs750383582 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696042 | TTGGGGGTGGGGGGA[G/T]GTGGAAATAACCTAT | 5607 |
rs750394639 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743743 | CCAGCACAGTGCCAG[A/G]TAAAATTAGATTGAT | 5607 |
rs750398026 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727954 | TCCTCAGGTAAGATT[A/G]TTCATTACTGCTGTT | 5607 |
rs750403926 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724632 | TTTTTACCTCCTCCC[A/G]ATAGAACTTGATAAA | 5607 |
rs750411619 | snp | A/T | 1.65976e-05 | 0.00288072 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67630891 | TTCTTCCCATAGAGC[A/T]TATCATGTCCCGAGT | 5607 |
rs750424036 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587067 | GAAAGATGAATGTTT[-/A]GATTTAGACTGGGTG | 5607 |
rs750468711 | snp | A/G | 1.76805e-05 | 0.0029732 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642498 | ATGGAGGACTTTGAG[A/G]TGAGCTTCATGGAGA | 5607 |
rs750475578 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784274 | TACTGCACAACATCA[A/G]AGCTACACCCGTTGT | 5607 |
rs750480543 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691861 | AGGATAAATGAAACA[A/G]AGACTAATAAGCACA | 5607 |
rs750484481 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642818 | ACATTAAGGTTCTTG[A/T]TCAAGGGAATGATAT | 5607 |
rs750488921 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696130 | AAAAGAGCTGAGCTT[-/T]TTTTTTTTTTTTTTT | 5607 |
rs750502928 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629067 | CAATACTTTGCCAAA[C/T]CATGAAACCAAGGTG | 5607 |
rs750508719 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771654 | GCTAATGGATGCAGT[A/G]TTTGAGAGGTGCATA | 5607 |
rs750524111 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610316 | TTATTTGGTCTACCC[G/T]TTGGGTGTCCTTATT | 5607 |
rs750554336 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725705 | TCTAACTCCAAATGG[A/G]AGTATATGCAAAAGT | 5607 |
rs750564339 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596937 | AGCACTTTGGGAGGC[C/T]GAGTCGGGCGGATCA | 5607 |
rs750565385 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574884 | AAAATAATAATAAAA[A/G]TAAAACAAAATAAAA | 5607 |
rs750608553 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705239 | TATTCATCCTTTCTA[C/T]ATTCATTTATGCATT | 5607 |
rs750612038 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623288 | AGTGTGAATAAACTT[A/G]TAGTAGTGGGCAAGA | 5607 |
rs750616192 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752315 | CAAGTGATCCGCCTA[C/T]CTTGGCCTCCCAAAG | 5607 |
rs750618732 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562495 | ATGTGGCCTCTGATG[A/T]TACTTACTCAAATTT | 5607 |
rs750641211 | snp | C/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719865 | CATGACTAAACTTTA[C/T]GTCTCTTTAACTCAG | 5607 |
rs750644378 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715498 | CTGTCGGGAACAACC[A/G]TGAGATTGACAAAAC | 5607 |
rs750655509 | snp | A/G | 6.97265e-05 | 0.0059041 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67806729 | GCTGGAGGAGAGGCG[A/G]AGCCAGCAGGGGCCC | 5607 |
rs750663318 | snp | G/T | 3.30044e-05 | 0.00406216 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563296 | AGATGAAGATGAAGA[G/T]GGTGATCGAATTACA | 5607 |
rs750707924 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753241 | TAAAAACTACAAAAT[A/T]CTCAAAAGGAAACAT | 5607 |
rs750716508 | snp | A/G | 3.30082e-05 | 0.00406239 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580718 | TTCCAGTATTCATAC[A/G]TTACTGAGTGATCTC | 5607 |
rs750735003 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579530 | AGGAGAGAATCACTT[C/T]CTTTACAGTTTGAAA | 5607 |
rs750752192 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715572 | TTTTGATGGATTTCA[A/G]ACTGATTTTAAAGTT | 5607 |
rs750755158 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666122 | CTTTAAAAGGGCAGT[A/G]CCATGGAAATTCGAG | 5607 |
rs750759677 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759457 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGGGAGGA | 5607 |
rs750769025 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546077 | TCAGAAAGGCCTGAC[A/G]AAGGACCTGTGGCAG | 5607 |
rs750786345 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632433 | CTATTATATTTAATC[C/T]TTAAAATTACATAGT | 5607 |
rs750793145 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802252 | GGTGGAGGAGGGAGC[A/G]GTGAGCAACCACAAT | 5607 |
rs750804247 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789072 | TAATCTCTAGAGATA[A/G]GCATTGTTAATAGTA | 5607 |
rs750805542 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603943 | TTTTCTTTAAAGTGT[A/G]ATAAAGCTAATAAGT | 5607 |
rs750820614 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778504 | TTAGGGCTATTGCAG[A/T]AGGGAGAGTGTTTAT | 5607 |
rs750821461 | in-del | -/A | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807372 | TCTCAGGCCCCCGCC[-/A]TGAGCTCCTTACTGG | 5607 |
rs750829922 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652064 | AAGCCATTTCAGCTG[G/T]AGTGAGAGGATATCT | 5607 |
rs750854847 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597676 | AAAAGCAGAAATACT[A/G]CTGGTTGATTGTAGA | 5607 |
rs750855809 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571192 | CCTTTTTGAAAATCT[C/G]TAGGAAGTTGTTTAT | 5607 |
rs750860469 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748828 | GGCTGGTCCTCAGGG[G/T]CATCAGATGCCCTAA | 5607 |
rs750864385 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692431 | TTAAAGAACAAACGC[C/T]GTAGATACATGGAAT | 5607 |
rs750866735 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786503 | TATGTCTCAGGAGCA[G/T]ACTAGACATGCCCAT | 5607 |
rs750875303 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692946 | CATTACAATGTGCAG[C/T]ACAAATTTTAATTAA | 5607 |
rs750881340 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726453 | CAAGCTGAGGGGTAT[A/C]ATTTTAAATCCAAGA | 5607 |
rs750882180 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772415 | TCGCTTCAAAAGTAG[A/C]ATTAGGATACATTTA | 5607 |
rs750884420 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758832 | AGGTTCCTTACATTA[C/T]ACTATCACTGATTTG | 5607 |
rs750901410 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584007 | TCCCACCACCACTTC[G/T]CCAAGTGCTGGGATG | 5607 |
rs750915794 | snp | C/T | 1.67091e-05 | 0.00289038 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592941 | CTTAAAGAAGTCTTC[C/T]GCTGAACTGAAAAAA | 5607 |
rs750928461 | snp | A/G | 1.96493e-05 | 0.00313436 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593016 | TCACATAATAATAAC[A/G]TATTACCGTCCAGTT | 5607 |
rs750930862 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550227 | ATTTATAAATTGATA[G/T]AAGTTTAATGATGAT | 5607 |
rs750935928 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800989 | GTTGAGTGTATGTTA[C/T]TTTTTTAAATCCGTT | 5607 |
rs750940520 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679353 | GGGTTGTCTCAACAC[A/G]ATACCAATTTCCACA | 5607 |
rs750943589 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570409 | CCATATGTGGACCCT[C/T]GGTCAAGTCTTTTAA | 5607 |
rs750957136 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652833 | CAAACAGCATTATAC[G/T]CTGTCTCTATGTGAC | 5607 |
rs751003827 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756272 | TCTCACCATCTTCTT[A/C]TGCTGCTTTCTTTGA | 5607 |
rs751012578 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660927 | GCTAAAAAATAAAAA[G/T]AGAGACTTATGAATG | 5607 |
rs751012708 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677515 | GGGACACACCGCTCC[A/G]AGTCAAGTCTGCTGT | 5607 |
rs751033638 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665082 | AGATGGGGTCTTGCT[C/G]TGTTGGCCAGGTTGT | 5607 |
rs751046325 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801982 | AGGTGTCATTAAATG[A/T]GCACTGGACTGGAAG | 5607 |
rs751056244 | in-del | -/C | 1.64762e-05 | 0.00287016 | frameshift-variant, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543363 | GCCCTTGGCCCCTTT[-/C]CTGCCATGGAGAACC | 5607 |
rs751059439 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647546 | GAGCCCAGGAGTTTG[A/G]GACCAGCATAAGCAA | 5607 |
rs751076588 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603673 | TATCCCTGGCTTTTA[A/G]TACAGTGCAAAGAAA | 5607 |
rs751081157 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786647 | TGAGTACAGAACTTG[A/G]AAAGTGGTGGTACAA | 5607 |
rs751086612 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769846 | GTAAACGTTATTTAC[A/G]CAAAGGGTCATAAGC | 5607 |
rs751090248 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744001 | TAACCCAGCCGTCAG[A/G]GTCAGGCCAGGCACT | 5607 |
rs751103769 | in-del | -/TAAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667414 | CATTTTTGCTTTCTC[-/TAAA]TGAATGATGATGGGA | 5607 |
rs751179422 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545556 | TGAGATTGTGACTGT[A/G]ATGAGAAAGATGGGT | 5607 |
rs751184681 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566375 | GAGATGGGATTTCTC[A/G]ATATTGGCCAGGCTG | 5607 |
rs751202507 | snp | C/T | 1.69209e-05 | 0.00290864 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592910 | CTTGCCACTAAAAAT[C/T]ATCTTTCCTTTTCAG | 5607 |
rs751204059 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689147 | GTAGTCCCTTTGACT[C/T]GGGAGGCTGAGGCAG | 5607 |
rs751211582 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768505 | GTTGTATGTAATGAT[A/G]TATTGCTCATCCAAA | 5607 |
rs751212265 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586878 | ACCCTCTCAACACAG[C/T]AGCCCAGCAGTCTCA | 5607 |
rs751231096 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710213 | TTGCTCTTTTCACTT[A/G]GATCTTCATTCTTTC | 5607 |
rs751234394 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546743 | TTTTTGTATTCTGTG[A/G]TCTCCAAGCTCAGAT | 5607 |
rs751266856 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581349 | TATGAGCTGATGAGA[G/T]TAAGTTTCAGTGAAT | 5607 |
rs751279770 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626815 | TGAGGTGGGAGGATC[A/G]CTTGAGCCCGGGAGT | 5607 |
rs751298099 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669500 | CCGGAGTGTTAGTGG[A/G]ACAGCAAAGAGGCCA | 5607 |
rs751321126 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637138 | GCTGCACTGTTGGCT[A/T]CCCTACTTTTGAGGT | 5607 |
rs751338563 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602230 | TTTTCCTGTGTTCTG[A/G]AGGTACTTAAGTTCA | 5607 |
rs751347350 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780273 | CAGGGAGCAGATACT[-/T]TTTTTTTTTTTTAAC | 5607 |
rs751356755 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721941 | TCCCATCTTTAATTT[A/G]CAGTGTATTATGATA | 5607 |
rs751361565 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635549 | TTCCTGTATTTACCA[A/G]TGCCAGTGCTCTTCA | 5607 |
rs751361934 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732842 | TGGTGCATCTGTCTG[C/T]GCCAGGCTTTTCACT | 5607 |
rs751368854 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553579 | TGGTGACTTTTTTTT[-/C]TGAACCAGAAATCCG | 5607 |
rs751378787 | in-del | -/AATAATAATAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686613 | GTCTCAAATAATAAT[-/AATAATAATAAT]AATAATAATAATAAT | 5607 |
rs751380805 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764033 | TTCTGGTGTTGAACA[C/T]CTGTTGGCTTGGTGG | 5607 |
rs751382402 | snp | C/T | 4.94254e-05 | 0.00497094 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727966 | ATTGTTCATTACTGC[C/T]GTTTGCCACTGTGAC | 5607 |
rs751393620 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588421 | GCACACCAGGGACCT[C/T]TCTAGGAATTCCTAT | 5607 |
rs751412812 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574092 | TGGCACGACATCCAA[C/G]AACCATCTCTTGGGG | 5607 |
rs751416120 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792254 | TCTAGGCAAAGTCCC[C/G]TTAATTGTTATGAGA | 5607 |
rs751421733 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805441 | TCCACATCCCTCCTG[G/T]CTTTGTGATGAGCTC | 5607 |
rs751426105 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622235 | CAAAGAAACAATATA[A/G]GACCTGAAGGAAGCA | 5607 |
rs751429783 | snp | A/G | 1.77269e-05 | 0.0029771 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642521 | CATGGAGACAATGGT[A/G]GCATTCAAGCTGGGT | 5607 |
rs751430797 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600716 | TACGATATCGGGACA[C/T]TCTTGGTCATGGCAA | 5607 |
rs751432489 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794805 | TTTGTGTAAATGGTT[C/T]GTTTCTCCCTGTTAA | 5607 |
rs751439891 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699128 | AATATGCTAGCTAAG[-/T]TTTTTTTTTTTTTTT | 5607 |
rs751455408 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787249 | TTTCTCAAATTTTGC[A/G]AAGGTCTCTAGCCAA | 5607 |
rs751460963 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724937 | GTACCTACTAGTTAA[A/G]ATCAAAGAACCATTC | 5607 |
rs751472309 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662765 | TAACTCAGGCTATGA[A/G]AGTGAAAAATGCAAA | 5607 |
rs751476091 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579699 | TTTATTTTCAAGAGG[-/A]AAAAAAAAACCCTTG | 5607 |
rs751510446 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770821 | CCTCTTAATAAAAAT[G/T]TCTCATGCAGTTTAT | 5607 |
rs751513949 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695410 | GCATGGTTTTTAAAG[A/G]AAGTTTATACTTTCT | 5607 |
rs751549517 | snp | A/G | 0.000162245 | 0.00900535 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646303 | ATTCTTTATAAGGTA[A/G]TTTTTTCATAATTTT | 5607 |
rs751549703 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556120 | CTATAAACTATTTGT[C/T]GTCTTTGCCTGTTTT | 5607 |
rs751550465 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611251 | TAGCCAATGAAACTT[A/T]ATAAGTGGTGGGGTA | 5607 |
rs751561944 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648437 | GCTGAATAACATTTC[C/G]TTGTATGGCTATACT | 5607 |
rs751579877 | snp | A/G | 1.65018e-05 | 0.00287239 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563336 | GATGAGGAAATGAAG[A/G]CAATGCTGTCATATG | 5607 |
rs751595389 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551803 | GCCTATTATAATGGA[C/T]TAATAAATTACTATT | 5607 |
rs751605785 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771854 | AAAAAGCATCCGTGT[-/G]ATTTTTCCAAGTGAT | 5607 |
rs751633047 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580743 | GATCTCTTTCTATAA[C/T]CTCTTTGCAGTATTA | 5607 |
rs751639937 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772846 | GAATTTGAAACAGCC[A/G]TAGGCTCTGAAAAGG | 5607 |
rs751645793 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632689 | ACAGTGAGAAATTGA[C/T]CTCTTTCTCTAACAG | 5607 |
rs751654735 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773781 | TATAACTCTGCAGGT[G/T]TCATGTCTAGAATAA | 5607 |
rs751680888 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666256 | CTTAGTAGCACAAAG[A/G]ACTATAGTGGATAGG | 5607 |
rs751696892 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716233 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 5607 |
rs751697182 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585263 | TGGAAAAGTACTAAC[C/G]TGTAACTCAAGATGG | 5607 |
rs751730037 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759759 | CATAACTGCGGGTGG[C/T]TAAAGGGAGACAGGA | 5607 |
rs751739360 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728470 | AGTCCATTATAGTAG[C/T]ATTGCTGACTCTAAT | 5607 |
rs751750262 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707369 | CAATTTAAAATCACT[A/G]TAGACAGAAGTGTGA | 5607 |
rs751750287 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692275 | TCTGTAGAAACCAGA[A/G]ATCGTTGAACGTGGA | 5607 |
rs751754199 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563649 | AGTACTTAAAGTAAC[A/G]GCTCATTAAAAATGA | 5607 |
rs751771565 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643885 | CTCTATTAGCAGTTT[A/G]TAATGCATAACTTAT | 5607 |
rs751776955 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684812 | ATATCTGAAATAAAA[A/G]TTTCATTGATGGAAT | 5607 |
rs751804112 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656008 | ATGCTGTTGATCCTC[C/T]CCAAAAATTTTCATT | 5607 |
rs751826414 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742294 | CTATATGTTTGGAAT[A/C]TTATAAAGTGAATTT | 5607 |
rs751832890 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688008 | GGGGTATTGCTACTG[C/G]ATACTACGTGGTTAG | 5607 |
rs751848693 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659501 | TTAGTGTGAAGTGCC[C/T]TGGGTGATGAGAACT | 5607 |
rs751858405 | snp | A/G | 1.65192e-05 | 0.00287391 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693587 | AGTAAACTTATGCAA[A/G]AATAATGTTTAAAAC | 5607 |
rs751861654 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726584 | GTCTTTGAAATAAGC[A/G]CAGAACTTCTCAAGA | 5607 |
rs751917175 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592516 | TGTGTAAGAGACCAG[C/G]ACTTAAATTATCTAT | 5607 |
rs751928061 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552371 | ACTTACTGTTGACAG[-/A]TGCTTTGCTAAGAGC | 5607 |
rs751937447 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733282 | TGATGTTATTCCAAA[C/T]GGCTTTTTAAGCTGT | 5607 |
rs751957423 | in-del | -/C | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719929 | TACCATGGAAAAAGA[-/C]CTTTGCCATTGTTTT | 5607 |
rs752003237 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619035 | TGTTTTCCTTACCTC[C/T]CTGACCTCATCTCCC | 5607 |
rs752003849 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606816 | AAATTGTCTAGTTAA[A/G]TGCTATTTAGTAAAC | 5607 |
rs752005695 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749071 | TCTAGGTCAACAGTT[C/G]AGCGTTAATTTCCTA | 5607 |
rs752010485 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572468 | TCAGAGTGAGTCCAC[A/G]GTGCAAAGTGAAAGT | 5607 |
rs752047907 | snp | A/G | 3.30104e-05 | 0.00406252 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543493 | GTAATCTCAGTGTCC[A/G]GATGCCAGCAAGGGG | 5607 |
rs752048890 | snp | C/T | 3.29598e-05 | 0.00405941 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600724 | CGGGACACTCTTGGT[C/T]ATGGCAACGGAGGCA | 5607 |
rs752067523 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559058 | CTCTGGTCCTGCCCA[C/T]GTCATTAACTCCGTG | 5607 |
rs752067817 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586073 | TGGGAGGTGGAGGGG[A/G]ATTCATCTGTAGTAT | 5607 |
rs752074399 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667846 | TACAGAATTTATTAA[A/G]CGTAGTTAATGGCTT | 5607 |
rs752090850 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663824 | AGGTTACAGTGTGCT[A/G]TGATTGCACCACTGC | 5607 |
rs752091317 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543387 | GAGAACCAGGTGCTG[A/G]TAATTCGCATCAAGA | 5607 |
rs752091686 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750165 | TGTTCTATTTAAGGG[A/G]TGAAGATTGATGAAG | 5607 |
rs752108597 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715779 | AAGAAGGCTGAACCT[C/G]CTGAAGCTAAAACAA | 5607 |
rs752127319 | snp | A/G | 9.93394e-05 | 0.00704697 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67769607 | TCCATCACAGGATTC[A/G]CCCGTCCTTCCAGTT | 5607 |
rs752129212 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716685 | GGAAGCTGGTCTCCA[G/T]GGAACTGTGCAGAAG | 5607 |
rs752145394 | in-del | -/ATTTTATGAA | 1.66333e-05 | 0.00288381 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630943 | GTAAGTACTGGATAC[-/ATTTTATGAA]ATTCTTGATGTTCAC | 5607 |
rs752149131 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649088 | AATTGTGGGCTTGTA[A/G]TGTGACATGGTATCC | 5607 |
rs752149480 | snp | A/G | | | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600695 | TGGAGATGAATGAAC[A/G]AGACATACGATATCG | 5607 |
rs752149492 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652189 | ATTCACCAGTGAAAT[C/T]ATCTGGTTCTGAGGT | 5607 |
rs752152844 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659578 | GCAGGTAGATTAGTA[-/T]GAAATTTGAGTACTT | 5607 |
rs752171599 | in-del | -/TAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595068 | TATGCTCTCAAGCAT[-/TAA]TAATGATTTGCCTTT | 5607 |
rs752195158 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602537 | GTGAATTTATTTTCC[A/T]AGCTTATTTCTAGAA | 5607 |
rs752203491 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569910 | GCATGGCCTGATAGT[A/C]CTGTTTTATTTAAGT | 5607 |
rs752207097 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573903 | CCATATGGTTTTTTG[C/G]TTTGTTATTTTACAT | 5607 |
rs752210694 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776908 | CATCTGCAAAACCGA[A/G]GGGGCAGCCCTTGAC | 5607 |
rs752249654 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616517 | TTCAGAGAATAGAGA[A/C]TCAGGGAATACAGGA | 5607 |
rs752260941 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788814 | CCCTGTCTCTACAAA[A/G]ACTTAAAAACTAGTT | 5607 |
rs752282764 | in-del | -/A | 3.30704e-05 | 0.00406622 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658513 | GTGCATTGTTCTGGT[-/A]AATTTCATTTGTAGT | 5607 |
rs752301056 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747361 | GTTCCTGAAAAGTTC[G/T]CTGTTAGAAAATGTA | 5607 |
rs752304330 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727996 | CATTCATTCCTATGT[A/G]TGAAGGTGCAGGGAG | 5607 |
rs752309287 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556293 | TTTTCCGTGGAGAAG[G/T]TTAAAATTTTTACAT | 5607 |
rs752309352 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712962 | TGACAACTTCTCATT[A/G]AAGAACCAAGTCAAG | 5607 |
rs752339616 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628923 | GGATTTAGTAATAAT[A/G]GAAGCAATTTTGGAG | 5607 |
rs752339702 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615187 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 5607 |
rs752343125 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648532 | TGAATAATGCTACTC[C/T]ATATATTTGTGTACA | 5607 |
rs752348899 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582509 | CATAGAAAACCCTAA[C/T]TGCAGTATCCTGGAG | 5607 |
rs752357445 | snp | A/G | 0.0003492 | 0.013209 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748521 | CACTCCACTGTAAAG[A/G]TATTGCATAGAGGCT | 5607 |
rs752373656 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677661 | AAGTAGGTTGTGCAG[A/G]AACACATTCCTCCAG | 5607 |
rs752387642 | snp | G/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548683 | ACTGGATTGCCTGTG[G/T]GCTTTATTCTGTACT | 5607 |
rs752389469 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721334 | TAAGTTTATATCAGT[A/G]GACTTTGGTGAGGAC | 5607 |
rs752393840 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711997 | AGAAAACAATTGTTA[A/G]TGTACTGGAGTAAAC | 5607 |
rs752396050 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568177 | ATGGCATACATTTTA[C/G]TGTAGTGCCTCCCAT | 5607 |
rs752409813 | in-del | -/ATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573750 | TGTCCTGATGTCCTG[-/ATA]TCTTAAGAACAAAAG | 5607 |
rs752426273 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806380 | CTTAAGCACCTTCCA[A/G]GCTAGTGCGAGCCTC | 5607 |
rs752426838 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727693 | TAATGTTTTGTTATT[-/A]AAATTAAAATATTTT | 5607 |
rs752427468 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746102 | TACAGTTTTAAGTTG[A/T]CTTAGACTAAGCTTT | 5607 |
rs752431590 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695513 | TTCCTTCCTCTACCA[A/T]GTTAGGTGAGATTGG | 5607 |
rs752436867 | in-del | -/TT | 9.88533e-05 | 0.00702971 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550093 | GAATGTAAGTCTGGC[-/TT]TTGTATACTTTCTTG | 5607 |
rs752441224 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706610 | ATCAGATTATGATCA[C/T]CAGAGAGGGTTGTTG | 5607 |
rs752452851 | in-del | -/ACCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760849 | ATCCACCATGATGGG[-/ACCT]ACACACCCTGAGCCC | 5607 |
rs752458830 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657798 | TGTATATGAATACAC[A/G]ATTTTTTTACAGATA | 5607 |
rs752474500 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673951 | CCTCCCAGGTTCAAA[C/T]GATTCTCCTGCCCCA | 5607 |
rs752499734 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796657 | TCCAAACTATTTAAC[A/G]TATCCGGTTTTTTCC | 5607 |
rs752500429 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592857 | CAAAGGTGTATTTCA[A/G]TCTGGAATTTTCAGT | 5607 |
rs752517711 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622147 | GAGGCTCCATCTCAA[-/A]AAAAAAAAAAAAAAA | 5607 |
rs752533765 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794860 | ATTTTAAAGGGGTAG[C/T]AGCCTTTACTTAATT | 5607 |
rs752534177 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588705 | ATCTTTTCTGATATG[A/G]CATTATTTCTAGTCC | 5607 |
rs752550095 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796111 | GCATTTTGTTGTTGA[G/T]GTTTTAAATTTTAAC | 5607 |
rs752554724 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580786 | GGAACAGCAAGTAAA[C/T]GGACAGTTAATAGAG | 5607 |
rs752578228 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777967 | TACAACAAGTTGGCA[C/T]GGGTCCTAGAAGGCG | 5607 |
rs752584453 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764275 | TGTATAAGGAGAAGG[A/G]AACAGGACCCAGACT | 5607 |
rs752608928 | snp | A/T | 1.66488e-05 | 0.00288515 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646416 | ATATCATTGGATTTT[A/T]TGGAGCATTTTTTGT | 5607 |
rs752622635 | in-del | -/CAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624575 | GGTAAAAAAATTAAA[-/CAT]CATCACGATCTCTTT | 5607 |
rs752641404 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603753 | AACTAAGTGTTTGAT[A/G]TGTTATGATTGAGTT | 5607 |
rs752660418 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684132 | ATAGGAGTTCCCTTG[C/T]GTCTGGCCTAACATC | 5607 |
rs752687774 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619172 | AGATGTCCGAATGGT[A/G]TGCCCCCATACTGCT | 5607 |
rs752688261 | snp | C/G | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720052 | AAAGTGTCTGTAAAG[C/G]TACAAAAGTGGGCAT | 5607 |
rs752698219 | snp | G/T | 1.90591e-05 | 0.00308693 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806858 | CTTTGCTGGGCCCTG[G/T]CTTCCCTGCCCTCGC | 5607 |
rs752703794 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670765 | TTTAAAGGATATCTA[C/T]AATGCCAGAAAGAGA | 5607 |
rs752725021 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805613 | GAGAGCTGGGGGGAG[C/G]GAGGAAGCGGCCGCT | 5607 |
rs752738518 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685705 | TTATAAATGAAATAC[C/T]CTAATATTACTTGAA | 5607 |
rs752777564 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762120 | GTGGATGTCAGTGGT[C/T]ATGCTTGATTATTTG | 5607 |
rs752786445 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761202 | ATGAACATTCTAACT[A/G]AACTTGTTCATTTCA | 5607 |
rs752791022 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791883 | AGGAGCAGCTATTAG[A/G]AAGATTCACTGATCT | 5607 |
rs752791610 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775277 | GTTTAGATATTTTAT[C/G]CCCTCTACTTTGTAT | 5607 |
rs752800941 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668960 | GAAAATGCTGGCCAG[A/G]TAGATTTGTGTTTAA | 5607 |
rs752826679 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599077 | CTAGTTTAGCATCTC[A/G]TCACTTTATGTGCTA | 5607 |
rs752845567 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620366 | ACAGAGCGAGACTCT[G/T]TCTCAGAACAGAAAC | 5607 |
rs752849475 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653625 | CATTTAAAATGAAAC[C/T]GACTTTTGGTTTCTT | 5607 |
rs752871008 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717018 | TGAATAGCTCAGGCA[A/G]CAGCAGTCAAGTATT | 5607 |
rs752878367 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750258 | AAAAATGTAACTTAG[A/G]CATATATTCCTGTTT | 5607 |
rs752884725 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551882 | ATTTTTTACATTTGT[A/G]CGGAAAGATATCTGT | 5607 |
rs752908057 | in-del | -/T/TT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650530 | TTTTTTTTTTTTTTA[-/T/TT]ATTATGAAAGGGTAT | 5607 |
rs752916557 | snp | C/T | | | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586881 | CTCTCAACACAGCAG[C/T]CCAGCAGTCTCAGAT | 5607 |
rs752936278 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67553300 | TATCCCCAAGTGTGT[C/T]AAAAGCCTGTTAAGT | 5607 |
rs752937922 | snp | A/G | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600731 | CTCTTGGTCATGGCA[A/G]CGGAGGCACAGTCTA | 5607 |
rs752938999 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629996 | TAATCCTAGCACTTT[C/G]GTAGACTGAGGTGGG | 5607 |
rs752943166 | snp | C/T | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547373 | TGGATCTGTCAGATA[C/T]TTGTCTGATTTATTG | 5607 |
rs752947318 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589791 | TGTGTGTATGTGTGT[A/G]TGTGTGTGTGTGTGT | 5607 |
rs752955971 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743612 | TAGGCAATGTATATA[A/C]AGCTTATCATGGAGC | 5607 |
rs752958700 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783324 | CCTCCCACCCTCACC[-/T]TACCCCTTCACCTCA | 5607 |
rs752962646 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802584 | GGCTCTCACTGCCTG[C/G]TGATGAGGCCAGCAA | 5607 |
rs752975455 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715853 | AAAGAAGGATTTTCT[C/G]ATGGATAGAACTCTA | 5607 |
rs752975505 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735873 | TTTGCTATTATCTCT[C/T]CCTCCTAGGCTCTGT | 5607 |
rs752975642 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767057 | CTGCTGGCTGTGGTT[C/T]TGCAAAGTCGACTTG | 5607 |
rs752976876 | snp | A/C | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681667 | AAACACCTAAACTTG[A/C]TATTTTTAATGCAAA | 5607 |
rs752982041 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555982 | GTAGATACGGGGTTT[C/G]ACCATGTTGACCAGA | 5607 |
rs752983812 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586193 | GATAATCCTAGGTGC[C/T]GGTATCTACAAAGAT | 5607 |
rs752992365 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641512 | ATGAATTGCCGTATT[C/T]ATACTGTATATTTTA | 5607 |
rs753018439 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647172 | AAATATTGTTAGTTC[C/G]TTGTGGAGATTCTCA | 5607 |
rs753064208 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690491 | TAGAGAAAACTAGAC[A/G]CCAAGAGACCAGGGA | 5607 |
rs753080513 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781518 | ATTTGGGCCTACCGT[C/T]CTCTATTTAATTTTC | 5607 |
rs753097417 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738459 | CATAGGAGGCAGCAA[A/G]TGACACACCCGACAA | 5607 |
rs753100694 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780399 | GAGGATCATGATCTT[A/G]TAATTCAGTGCCTAT | 5607 |
rs753103915 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594964 | TCAATAAATTTCTGG[G/T]CTGAACACTGACACC | 5607 |
rs753132535 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805161 | GGCATCTTCGAAGCC[A/G]AGTTTCCTCCTCCTC | 5607 |
rs753146166 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666138 | CCATGGAAATTCGAG[-/T]GTTGTTAGAAAGTGA | 5607 |
rs753157797 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689640 | ACAGTAGGCTTACAT[A/G]TATGTTAAAAAGATG | 5607 |
rs753166931 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793269 | TCAGGGCAACACTGT[A/G]AGACCTCATCTCTAA | 5607 |
rs753176003 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561029 | TTGAAATTCAAATAT[A/G]AGCAGTCTCTTTTTA | 5607 |
rs753187611 | snp | A/G | 8.23798e-05 | 0.00641741 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67550042 | TGTTTAGGATGTGAT[A/G]GGCCAGGTTCTGCCT | 5607 |
rs753201811 | in-del | -/AATAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638553 | TGCGTGTGTCTTTAT[-/AATAG]AATGCTTTATATTCA | 5607 |
rs753221756 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560302 | AGCCACCAGTCTTCT[C/T]ATGGGTATGGTTACT | 5607 |
rs753222259 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737405 | GGGGACAGACCTGGC[C/T]GAGCTTTGTTTGAGC | 5607 |
rs753223905 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709346 | TTGTAAAATTCCTGA[A/G]CTAGGACAAACTAGG | 5607 |
rs753225181 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652632 | TTTCAACATGAGTTT[G/T]GAAGGGGACAAATAT | 5607 |
rs753228839 | snp | A/G | 1.66294e-05 | 0.00288347 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772679 | AATGACACAGATAAC[A/G]TAAGGGGTTTTTTTC | 5607 |
rs753231117 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573643 | CCGCAGCCCCAGGAA[A/G]TCAGGCATTCTTAGT | 5607 |
rs753245576 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685951 | ACAACAAAAAGCTTA[C/T]AGCTCTCAAAGCCTG | 5607 |
rs753252809 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67622531 | TTAAATGCATGTGGA[-/T]TTTTTTTTTTGTAAA | 5607 |
rs753264118 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778314 | TAAATTGCACATCTG[C/T]GTGGTCCCTTTAAAA | 5607 |
rs753267891 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704904 | GTAGAGATAAGAATC[C/T]TAGATTGGGAATGGA | 5607 |
rs753272355 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651792 | TGATTTCATATCTTG[A/G]CTATTGTGAATAGTG | 5607 |
rs753280075 | snp | C/T | 6.5999e-05 | 0.00574414 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658593 | AATGCCAGAACATGT[C/T]CTTGGAAGAATTGCA | 5607 |
rs753281931 | snp | C/T | 1.68661e-05 | 0.00290392 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772792 | TAGAATTCTCAGTTA[C/T]ATATTTATGTTTAAC | 5607 |
rs753302587 | in-del | -/CTTCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716654 | TGTTAAATCAGACCA[-/CTTCT]CTTAGCAGTGAGGAA | 5607 |
rs753336851 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543373 | CCTTTCCTGCCATGG[A/T]GAACCAGGTGCTGGT | 5607 |
rs753369185 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545588 | TTCTCTTACTCATTT[A/G]AAACAATGGAAGGTT | 5607 |
rs753372243 | in-del | -/GAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596242 | CCTGGCCAACATGGT[-/GAA]ACCTCTTCTCTACTA | 5607 |
rs753376622 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759363 | CAGGAGTTCGAGACC[A/G]GACCTGGCAACATGG | 5607 |
rs753395023 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789036 | GTTAGTCTCCTTCCA[A/G]TCCTCCATATCTTCC | 5607 |
rs753407439 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698175 | TTATATTAAATTAAC[C/G]ATTTTTCAGAAATTC | 5607 |
rs753407547 | in-del | -/A | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719084 | CCTCTGGTAACCATC[-/A]ATTCTACTGTCTATC | 5607 |
rs753468524 | snp | C/T | 4.9657e-05 | 0.00498257 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748650 | AGTCATTCCTAATGG[C/T]GTGGAAAGCTTATAT | 5607 |
rs753469685 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796944 | GGACAGAATTTCTAG[A/G]AACCGGCACACATTG | 5607 |
rs753471383 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747525 | AGCTTTGTAAGAAAT[A/G]CAGTTTATCAGTGTT | 5607 |
rs753480361 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714242 | CATGAACACTTTTAT[G/T]TAACATTAGCAACCA | 5607 |
rs753484465 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699360 | GGAGATTTTCTGTTC[C/T]CTGCTAGAAGCCTAA | 5607 |
rs753494390 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571051 | AGTTGGAAGGTATGA[C/T]CAATGAGAGTCGTTA | 5607 |
rs753497439 | snp | A/G | 1.65806e-05 | 0.00287924 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769595 | ACATGTTTTTCCTCC[A/G]TCACAGGATTCGCCC | 5607 |
rs753505829 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570127 | TCCTTCTGCCAACAC[A/G]TATTACCTTAAACAT | 5607 |
rs753508738 | snp | A/G | 1.66515e-05 | 0.00288539 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646448 | GAAAACAGGATTTCA[A/G]TATGTACAGAATTCA | 5607 |
rs753523276 | in-del | -/TTTATG | 1.69049e-05 | 0.00290726 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772796 | ATTCTCAGTTATATA[-/TTTATG]TTTAACATTCTGTTT | 5607 |
rs753527640 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709536 | ATGAGTTTGTTATAT[A/G]ATAAGGGCTTTACCA | 5607 |
rs753556090 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558099 | AGTCATTTCTTATTA[A/G]TAGTCTTGCTAATTT | 5607 |
rs753557910 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700659 | AATGTTTTGCTGCTC[A/G]TCTTGTGTCTAAATC | 5607 |
rs753560502 | snp | C/T | 4.95315e-05 | 0.00497627 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658550 | GCATGTTTATCTCTA[C/T]AGGGGGATCTTTGGA | 5607 |
rs753565304 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797614 | ACTATAGTTTTTCTA[C/G]GTATAGATTTTATAT | 5607 |
rs753576656 | in-del | -/GGC | 1.6591e-05 | 0.00288015 | cds-indel, intron-variant | MAP2K5 | GRCh38.p7 | 15:67664605 | ATTTAGGTTGTTAAA[-/GGC]GGCCTTACTTATTTG | 5607 |
rs753611961 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777221 | AGCTGTCAGGCAGCC[C/T]TTTAACTTCCCTGCC | 5607 |
rs753627881 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626418 | TGTAATCCCAGCTCC[C/T]TGGGAGGCTGAGGCA | 5607 |
rs753632890 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659695 | TCTTGGCTGTAAAGT[G/T]TAATAACATGTATAA | 5607 |
rs753634255 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566270 | ACCTCCGCCTCCTGG[A/G]TTCAAGTGATTCTCA | 5607 |
rs753666984 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798952 | AAAGCAGGTGCATCA[C/T]GAGGTCAGGGGTTCA | 5607 |
rs753672217 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577973 | CCACTGTACTCTAGC[C/G]TGGGTGACAGAGCAA | 5607 |
rs753690431 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565453 | CAGGCTGGTCTCAAA[C/T]TCCTGACCCCGTGAT | 5607 |
rs753693390 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785446 | CACAGGACGACTACT[A/T]GAGTGGCACAGCTGT | 5607 |
rs753695932 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795172 | TTATGTATCTTTTTT[-/C]CCCTTCTTGATATTT | 5607 |
rs753700788 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674143 | TGAGCCACCGTGCCC[A/G]GCCCCAAACACTTTT | 5607 |
rs753712955 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753856 | TTCCACCTCTAGGTA[C/T]ATATCCAAGAGAATA | 5607 |
rs753718787 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625333 | GGGCTGAGACTGTTC[C/T]CAGAAGGCCTGTGCT | 5607 |
rs753719773 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645563 | CCACAAGATAGTTCT[A/T]TTTTTTAAGAGACAG | 5607 |
rs753759520 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592303 | CACCTGCTATGGACA[A/G]GACACAGTGCTAGAT | 5607 |
rs753778232 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564105 | ACAAAACCTTTTCCC[A/G]TGGCCTGGTAGAAAG | 5607 |
rs753778260 | snp | G/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719960 | TAACTGACTTTTAGA[G/T]ATTTAGTTATATACC | 5607 |
rs753788964 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687545 | TCATGTTTCTCTCCA[C/T]AGCACCTAGTACCAT | 5607 |
rs753817392 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707476 | CTTCTGTTTATTCTC[A/C]CTTGTAAAAACAAAA | 5607 |
rs753819712 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579208 | AAAAGAATACCTGAG[C/G]AATGTTCCAAATAGC | 5607 |
rs753835163 | snp | C/T | 1.6674e-05 | 0.00288734 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693608 | TGTTTAAAACCAACA[C/T]CTTTATCTTTATGTA | 5607 |
rs753855701 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654725 | CAATTAACTTCTTAA[C/T]TTATAACAATTTAGT | 5607 |
rs753858336 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796192 | CTTGAGTTTTTTGTA[C/T]AGTCCTATTTTGTAC | 5607 |
rs753867269 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794176 | AATGCAGGTCACACC[A/G]GTCACCACCATCAAA | 5607 |
rs753875781 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614180 | ATAGGAATCGTGAAG[C/G]ATTCAGTAACCTCAC | 5607 |
rs753898149 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657903 | TGACATACTTCATGT[A/T]TAGTACCTTATGAGG | 5607 |
rs753920549 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589296 | AAAGTTGATAGCCAG[A/G]TACTAGCATAATGAA | 5607 |
rs753941258 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751222 | AATAAGAACCATGAC[C/T]ATGAAACTCAGACCA | 5607 |
rs753946377 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694653 | GGAACACTTTTACAC[-/T]GTTGGTGGGACTGTA | 5607 |
rs753946500 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655623 | GAAATGTCACTTCTC[G/T]TGCTGCTTTCAAGAT | 5607 |
rs753955133 | in-del | -/TCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556258 | TTCGGTTTGTTCTGG[-/TCT]TCTTATTCTCTCTTC | 5607 |
rs753959413 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587167 | CGGAGGGAAGAGGGT[A/G]GGTGAAGGCCCTGAG | 5607 |
rs753981872 | snp | C/T | 1.67206e-05 | 0.00289137 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630876 | TGATTTTGTTTTTTT[C/T]TCTTCCCATAGAGCA | 5607 |
rs753983093 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788974 | GAGACCCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 5607 |
rs753989662 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682938 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 5607 |
rs753989723 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717392 | AGTAAATATTTATCA[A/G]GTACTACCCAGTGTT | 5607 |
rs754011019 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703511 | AAATAAACCTTCAGC[A/G]TGTTATATAGATGTA | 5607 |
rs754014957 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600747 | CGGAGGCACAGTCTA[C/T]AAGTGAGTAGTCAAT | 5607 |
rs754040153 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561191 | TAAAGAGAATTTGAC[C/T]TGGTTTTAAAGCAAA | 5607 |
rs754044767 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731299 | TGTACCCAGTGAGGT[C/T]GCAGAGAGGGAGGAG | 5607 |
rs754054413 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762398 | ATAAAAAGAGAAAAA[A/C]GATGCTCATTGGCTT | 5607 |
rs754059332 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662616 | CTTTTATAGCAATTT[A/G]TACATAAAGATTTTT | 5607 |
rs754062657 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635465 | CAGGTGTGAGTCACC[A/G]TGCCCGGCCTGGAAA | 5607 |
rs754127521 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805239 | AGGGTGTCCCCAGGG[C/G]AGGTTTCCCAACCTC | 5607 |
rs754148022 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629008 | GACCCGTGAAGGGAG[A/G]AAACTTTGGAGGCAG | 5607 |
rs754166523 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574696 | ACATGGGGAAACCCC[A/G]TCTCTACTAAAAATA | 5607 |
rs754169447 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771549 | AAATGATAGTGGGTA[A/G]TAGCCTTGTTTTCCC | 5607 |
rs754169921 | snp | A/G | 3.3112e-05 | 0.00406877 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563271 | TCATTTGCATTATGT[A/G]CTTTTAAACAGATGA | 5607 |
rs754198070 | in-del | -/CGCCGCTACCGCCGTCGCCGC | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542721 | TCCTCCTCCTCCTCT[-/CGCCGCTACCGCCGTCGCCGC]CGCCGCTACCGCCGT | 5607 |
rs754231716 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728685 | TGGTCTGTACAGGCC[-/A]AAGTGCCTAGAGGCA | 5607 |
rs754241638 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609378 | TGAAGTAAGATTATA[A/G]AATCTATAGGTCTAT | 5607 |
rs754245808 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788031 | CACAGCACCGTCCTA[A/G]GGTGTGGAGACTGTT | 5607 |
rs754262480 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610215 | GAAAGTCAATGATGT[A/T]TCATCTCTAGGTGTT | 5607 |
rs754266491 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706332 | TCTGTGGAGGACTGA[A/T]GAAAACAGACTCATT | 5607 |
rs754268497 | snp | A/G | 9.89364e-05 | 0.00703267 | missense | MAP2K5 | GRCh38.p7 | 15:67806721 | TGCCGGGCGCTGGAG[A/G]AGAGGCGGAGCCAGC | 5607 |
rs754271455 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800749 | GGCTCAGTGTACCTG[A/G]GCTTTGGTGCACTCA | 5607 |
rs754276193 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726245 | GTGTGGGCCTTTTCA[A/G]AGTAGTCACTTTACG | 5607 |
rs754290818 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806521 | TGGAGCTGATAGCCT[C/T]CCTCGTTACCTCACA | 5607 |
rs754302719 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595238 | ATAAATATTTATTTC[C/T]TTTCTGTCACTCAGA | 5607 |
rs754309895 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713075 | TTTAATGTTATAACA[G/T]GGGAAAAATATATGT | 5607 |
rs754337968 | snp | C/T | 1.67072e-05 | 0.00289021 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664588 | CTGTTTTCTTTTTCC[C/T]AAATTTAGGTTGTTA | 5607 |
rs754348694 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642499 | TGGAGGACTTTGAGG[A/T]GAGCTTCATGGAGAC | 5607 |
rs754350040 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547671 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 5607 |
rs754356677 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652895 | ACAGTATTTGTCTTA[-/T]TGTGTCTGGCTTATT | 5607 |
rs754377373 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562270 | GATGAAGAGTTAACT[A/G]TATATTTGGAAATAG | 5607 |
rs754394717 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648871 | GGTGTGAGCCACTGC[A/G]CCCGGTCAGTGTTTT | 5607 |
rs754435731 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578483 | TGGAACATAAGCTTC[G/T]CTATTAATACAGACA | 5607 |
rs754439187 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667949 | ATCTGAGCAATAAGC[-/A]GCGGCAAACCACTCA | 5607 |
rs754443603 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599516 | AAAATATTTCCCTTG[A/G]TAAATGAACCCTTGC | 5607 |
rs754460218 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647547 | AGCCCAGGAGTTTGA[G/T]ACCAGCATAAGCAAT | 5607 |
rs754468335 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615034 | CAGAGTTTTGCTCTT[A/G]TTGCCCAGGCTGGAG | 5607 |
rs754489069 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711847 | CAGGAATTGGTGGGA[C/T]GAGATATGTGGAGCC | 5607 |
rs754516401 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696244 | CAGTTCTCAGGCCAA[A/G]TTCAATTTACTGGAA | 5607 |
rs754520679 | snp | A/G | 1.70708e-05 | 0.00292149 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664560 | CTTTTAAAAACCATA[A/G]TTGATAATTGTACTG | 5607 |
rs754521186 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730270 | ATGTGTATTTTTATA[A/G]TGTCACTGAGGCTGA | 5607 |
rs754524452 | snp | C/G | 1.65288e-05 | 0.00287474 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703444 | CGCTTCTGTGCATAT[C/G]TGTACTAATATATTC | 5607 |
rs754529038 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757574 | AACCTGTGTTAATCC[C/G]AGAGCTCGGTACCGG | 5607 |
rs754533905 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662547 | CTTGAAATTGGTAAG[C/T]TCACGCTCATGTGCA | 5607 |
rs754539722 | in-del | -/AGT | 1.64754e-05 | 0.00287009 | cds-indel, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543431 | CGCGGTGGACTGGAC[-/AGT]GCACTCCGGGCCGCA | 5607 |
rs754553523 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567966 | CTTTCATTAAGAAAT[A/T]CAGCCAATACATCTT | 5607 |
rs754559703 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554406 | CTAACACTAATTGAT[A/G]TCTTATATAAAAGAA | 5607 |
rs754571350 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797795 | TCAAGCAGTTCTCCA[G/T]CCTCAGCCTCTGGAG | 5607 |
rs754606328 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696970 | GGCAACAAGAGTGAA[A/G]CTCAGTCTCAAAAAG | 5607 |
rs754611689 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676392 | GCTAAATTGGAAGTC[A/G]TCTTTTGTTCCCCTT | 5607 |
rs754616177 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542583 | TCCCACGCCGGGGGC[A/G]CATCCTCCCGGGAGC | 5607 |
rs754622853 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722744 | TGTGTCTGAGTGTTC[C/T]AAAGTGGCTGCTGCA | 5607 |
rs754630786 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613746 | AAGCTTCTCCATACT[A/C]ATTTTATCTAGTGTG | 5607 |
rs754651789 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589786 | GTGTGTGTGTGTATG[-/TG]TGTGTGTGTGTGTGT | 5607 |
rs754663363 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751552 | CTGATATCTTTGGGG[A/G]ATAAGTCGGCCCCTA | 5607 |
rs754714483 | snp | A/T | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541009 | TAGAAAATCTCTAGT[A/T]TCGTGGTCTATTTTC | 5607 |
rs754724868 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628143 | GATTCTCAAAGACCC[A/G]GTGCCCACTTAACTG | 5607 |
rs754727362 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756327 | GAGACAAAGTAAAGA[C/T]ACACATAAGTTTTGA | 5607 |
rs754738242 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718835 | TATTTTGATACAGGC[A/G]TACAATGTGTAATAA | 5607 |
rs754742576 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588458 | CCCTTCTTCCTTGTA[G/T]TGTAGTAGTGAGCAC | 5607 |
rs754758691 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727989 | ACTGTGACATTCATT[A/C]CTATGTATGAAGGTG | 5607 |
rs754762409 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793491 | CTTTAACACACCTTC[A/G]TCTTCTCCTTCTATT | 5607 |
rs754780193 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555401 | ATCCACCCCCACGAC[-/AA]AAACACCTCCTTCCA | 5607 |
rs754813250 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748281 | TATGAGTTCAGAAAA[A/C]AATTCACTTTTCTTT | 5607 |
rs754823926 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752327 | CTACCTTGGCCTCCC[A/G]AAGTGCTGATTTCAT | 5607 |
rs754824624 | snp | A/G | 7.23877e-05 | 0.0060157 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646313 | AGGTAATTTTTTCAT[A/G]ATTTTTATTTGTAAA | 5607 |
rs754826231 | snp | A/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719881 | GTCTCTTTAACTCAG[A/T]GTCTCTCACGAATTT | 5607 |
rs754850048 | snp | G/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670998 | CTAAGAAGGAATAAG[G/T]CTTTATCTGACATTC | 5607 |
rs754862631 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749404 | CAATGTTTATTTTTT[-/A]AACTTTAATTTTATA | 5607 |
rs754869892 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648826 | CCTCGTGATCTCCCC[A/G]CCTTGGCCTCCCGAG | 5607 |
rs754872347 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695459 | ATAATAAATTAACCT[C/G]TGAAGTCTTCATATC | 5607 |
rs754879577 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775570 | GACTCAGCAGAAGAT[A/G]TAAAGTAGAGGAAGC | 5607 |
rs754883838 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667651 | TCTTAAAAACCAGAG[-/T]TAAAAAAAAAAAGAA | 5607 |
rs754889936 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635594 | TCAGATTTCCATCTA[A/G]TAGTATTTTCCTTCT | 5607 |
rs754901559 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662852 | CCTTGCCTTGTCAAC[A/G]TATATGCTTTGCACC | 5607 |
rs754902387 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669569 | CAGCTGTTAGGAAAA[C/T]GTTTTGGTAATTCAG | 5607 |
rs754948387 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759958 | TCGGCGATATTGTCA[A/G]CTAGACCTGTGTTTC | 5607 |
rs754974968 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67632716 | ACAGTTGCATAGTAT[A/G]TATTTCTGCATCTTT | 5607 |
rs754977532 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804735 | TGGGGGGAGGGGCCC[A/G]TCACTCGTGAGCACA | 5607 |
rs754980783 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618153 | ATTTCAAGGAGTAAA[A/T]AATATAATCAGTTGG | 5607 |
rs754991388 | snp | C/T | 0.000178333 | 0.00944111 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806757 | CCCCCGTGAGGCTGC[C/T]GCAGGGCACTGAAAG | 5607 |
rs754993109 | in-del | -/ATCTTT | 0.000349357 | 0.013212 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693607 | ATGTTTAAAACCAAC[-/ATCTTT]ATCTTTATGTACTTG | 5607 |
rs755000233 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560055 | AGCCTGAATCTTGGC[C/T]AGATGGGCTGTATAT | 5607 |
rs755060738 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666304 | TTCTGCCATTATCTT[C/G]ATTTTTCTTCTTTAA | 5607 |
rs755063026 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685044 | AAAAATAATTTGAAG[A/C]AATAATGGCTGAAAA | 5607 |
rs755072870 | in-del | -/TTAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782491 | TCATACAGCCTGATT[-/TTAG]TTAATTTTTTTTTCA | 5607 |
rs755074369 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749092 | TAATTTCCTAATTAG[A/G]CATTTTTCTCAGAAT | 5607 |
rs755081543 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728559 | AGCTATTTTGTGGTT[G/T]GAAAATGATTCCCCA | 5607 |
rs755083356 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613741 | TAGGGAAGCTTCTCC[A/G]TACTCATTTTATCTA | 5607 |
rs755085005 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692464 | GTTACATGGCCTTTT[C/T]TGGTCCCTTTTTAGA | 5607 |
rs755106662 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761146 | TCCCTGATGTTTTGA[A/G]GTCCAGAGTAGCAGA | 5607 |
rs755112107 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742346 | ACTAGGTGACTTCCA[A/C]CATCATGTAGAGGAT | 5607 |
rs755113876 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653341 | CCCAGGCTAGAGTAC[A/C]ATGGCACAATGTCAG | 5607 |
rs755121537 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579964 | ATTTTTCCACTAGGA[A/G]CATCACTTTGTTATT | 5607 |
rs755135893 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693116 | TCAAAGTCTGTTATC[C/T]CTCCAGCGTATTTAG | 5607 |
rs755138084 | snp | A/C/G/T | 0.0038799 | 0.0438982 | synonymous-codon, missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592959 | TGAACTGAAAAAAAT[A/C/G/T]CTAGCCAATGGCCAG | 5607 |
rs755160112 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550544 | GGAACACTTCAGGTC[A/T]TTAGTCCTTCCTTTT | 5607 |
rs755198819 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771752 | CCAAATGATCATTAA[A/G]TCTATTTTTAAAAAA | 5607 |
rs755211772 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550793 | TTTTTTTTTTTTGCC[A/G]CAGACTCTCACTGTG | 5607 |
rs755279236 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552373 | TTACTGTTGACAGAT[A/G]CTTTGCTAAGAGCAT | 5607 |
rs755299907 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593325 | AAAGGAAAAACCATT[A/G]CTTTCTCACCTTAGC | 5607 |
rs755310803 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763043 | AATTGAATCATCTTT[C/T]ACTTTCTCTGCTCAA | 5607 |
rs755314675 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584063 | CATAATTCTGATGTA[A/G]TAACATGTTCTCCTC | 5607 |
rs755317267 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592530 | GGACTTAAATTATCT[A/G]TTTTGTCTTTTGAAG | 5607 |
rs755330049 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544579 | CCTACATGTTGCAGC[C/T]GCTTCTAATCTTTCT | 5607 |
rs755339472 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767411 | GATAGCAGGCTTTTA[G/T]TTTCCTAAATATTGC | 5607 |
rs755339685 | in-del | -/GAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733380 | ATCTGTTTCAAATAA[-/GAT]GATAAGTAGTAAAAA | 5607 |
rs755341132 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707688 | GAGCCACAAGGGGAA[-/G]GGGGGTGGGGTTTCA | 5607 |
rs755346707 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543404 | AATTCGCATCAAGAT[C/G]CCAAATAGTGGCGCG | 5607 |
rs755349621 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640013 | TGTATATGTCTTTTA[A/G]GGGTGTTATCACCAA | 5607 |
rs755372351 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580026 | AGCCATCTCCAAGTT[A/G]GGTGGACATATGCTT | 5607 |
rs755373254 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675737 | CTTTCTGTAGTTACC[A/T]GTATTCAGAAGGTCA | 5607 |
rs755383198 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545581 | ATGGGTTTTCTCTTA[C/T]TCATTTAAAACAATG | 5607 |
rs755427339 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768535 | ATGGCCAAAGCACTC[C/T]AAAGCACAGTGAGAT | 5607 |
rs755447967 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702260 | GTTTATGAATCTGAA[A/T]TGAGATATGCATGAA | 5607 |
rs755452133 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572501 | GTTTATTAAGAAAGT[A/G]AAGTGGTGAAAGAAT | 5607 |
rs755459775 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627928 | GAACTTTGAAACAAC[C/T]GATGAGAGCCTGAGG | 5607 |
rs755462968 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619141 | CTGTTTCCTCTACCT[A/G]GAATCCCCTTCCCCT | 5607 |
rs755463668 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703171 | TATAGATCATCTATA[G/T]ACTGTATGCACAAAT | 5607 |
rs755467558 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67567610 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 5607 |
rs755471825 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543506 | CCGGATGCCAGCAAG[A/G]GGGACTCAGGGACTT | 5607 |
rs755476231 | snp | C/T | 1.6554e-05 | 0.00287693 | missense | MAP2K5 | GRCh38.p7 | 15:67769609 | CATCACAGGATTCGC[C/T]CGTCCTTCCAGTTGG | 5607 |
rs755499143 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667927 | GAGGACTGTAGAGTA[C/G]AATGAAATCTGAGCA | 5607 |
rs755499858 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791719 | GGGGTTGTTGTGACA[C/T]TGAAATAAGATAATG | 5607 |
rs755533065 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688016 | GCTACTGCATACTAC[A/G]TGGTTAGGAAAGGCT | 5607 |
rs755560492 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776948 | GTGACTTTAGGAAGT[C/T]AGAACCCCAGAAATT | 5607 |
rs755573394 | in-del | -/TAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67697349 | CTATGACATAGGTAA[-/TAT]TATTATTCTCATTTT | 5607 |
rs755579725 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779715 | CTCTAATGCCTCTTT[C/T]GTGTTTTATTGGACT | 5607 |
rs755603984 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602540 | AATTTATTTTCCTAG[C/T]TTATTTCTAGAAGGG | 5607 |
rs755626571 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67699215 | TTTTTGAATGAAATC[C/G]TACCACAGAGAGGAA | 5607 |
rs755647036 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731728 | TGCTTTAGGCAGGAA[G/T]GGGTACAGTTAGGTC | 5607 |
rs755657699 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727719 | ATTTTATCAGGGGTG[C/T]AACATCGTCCATTGA | 5607 |
rs755661687 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568227 | TTTAGTACAAGAGTC[C/G]TTATATTTAAGTGAA | 5607 |
rs755663482 | snp | A/C | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719030 | ATTTTTGTACCCATT[A/C]ATCATCCCCACTCTT | 5607 |
rs755670284 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747469 | TTTAGTACTTTAATG[A/T]CTAAGTGGATGTTTT | 5607 |
rs755678613 | snp | A/G | 0.000384966 | 0.0138685 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592930 | TTCCTTTTCAGCTTA[A/G]AGAAGTCTTCTGCTG | 5607 |
rs755696535 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786756 | CCTCTAGTTGCTTAT[C/G]TACAAAAATAGAGTA | 5607 |
rs755714085 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623817 | GGTCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG | 5607 |
rs755717418 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597695 | GTTGATTGTAGATCC[C/T]TTTAATGATTTTTTC | 5607 |
rs755717698 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590740 | ATTACAGGCTTGAGA[C/T]GCTGTGCTTGGCCCC | 5607 |
rs755733735 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541107 | CAGAAGTGAAGTGCA[A/G]GTGAAAAGGGGAAAT | 5607 |
rs755739176 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624338 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 5607 |
rs755759793 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601303 | AGTGATCTTACCCCA[A/G]AGGAATGTTCATTTT | 5607 |
rs755760036 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795307 | TTTTGTTCTTTTTAT[-/A]ATGTATTAAACACTT | 5607 |
rs755771255 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649095 | GGCTTGTAGTGTGAC[A/G]TGGTATCCCATTTTG | 5607 |
rs755825219 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610587 | CCAAAAGGCATTTAC[C/T]GCGTATAACTTTCTG | 5607 |
rs755834698 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775647 | AATGAAGTAACTAGT[A/G]TAAAAGAACTGCAGG | 5607 |
rs755843834 | in-del | -/T | 3.29785e-05 | 0.00406056 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550128 | TCCTTTCTGCAGTCA[-/T]TTTTTTAAAGGGTTT | 5607 |
rs755853091 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683315 | AGATTTAAAGGGATT[C/T]TATTTGCTTCAAATT | 5607 |
rs755856013 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67739959 | AGAAACATTACCATG[G/T]GGTAGGGAGCTTTAG | 5607 |
rs755866635 | in-del | -/CACTGTGAGAATACATTTTTACA | 7.82626e-05 | 0.00625501 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658757 | TTCTCCTGTTTTGTT[-/CACTGTGAGAATACATTTTTACA]CTTCTTTTCATAGAC | 5607 |
rs755866650 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787931 | GCATTTAAAAATGTT[A/G]CTGCAGTCTATTACC | 5607 |
rs755869288 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67746231 | TGGGGACAGTGTTTC[A/T]TAATCCATTTCTGAA | 5607 |
rs755875764 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577891 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 5607 |
rs755881969 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706618 | ATGATCATCAGAGAG[A/G]GTTGTTGAGCACCTC | 5607 |
rs755894464 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759396 | AGACCCGATCTCTAC[-/A]AAAAAAAACAAAAAT | 5607 |
rs755913836 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643096 | TTTTGGGGTAAAGCC[C/T]GCACCTTGGGATTTT | 5607 |
rs755921213 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796662 | ACTATTTAACATATC[C/T]GGTTTTTTCCTTCAC | 5607 |
rs755926686 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783499 | CCTCTGTGAAGCTTT[C/G]CTAAGCGTGCTTCAG | 5607 |
rs755934983 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742825 | GCTCTTATACACCTA[A/T]GTGGTGTGGGACATG | 5607 |
rs755946257 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67685833 | AAAAATTGGGCCTTC[A/G]CCTGTTTTTACAAAC | 5607 |
rs755949858 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67741616 | ACCCTAGAGCTGGGG[G/T]TGAAGTCATCTTCCC | 5607 |
rs755961794 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596934 | CCCAGCACTTTGGGA[A/G]GCCGAGTCGGGCGGA | 5607 |
rs755989034 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805614 | AGAGCTGGGGGGAGC[A/G]AGGAAGCGGCCGCTG | 5607 |
rs755992336 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744589 | TAGGTAGATTCATTT[C/T]AGTTTTCTGATTGTG | 5607 |
rs756000876 | in-del | -/A | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67671270 | GAGGGGAGAATTTCC[-/A]AGAGTAGATTTTGTG | 5607 |
rs756005360 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67707404 | CAATAGCATTTTAGA[A/G]TCTGAGGAACAAAGT | 5607 |
rs756052971 | snp | A/C/T | 7.77928e-05 | 0.00623628 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806867 | GCCCTGGCTTCCCTG[A/C/T]CCTCGCCTTCACCTC | 5607 |
rs756054464 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623450 | ATATTGCAAACTTTT[A/G]CCAGTTCTTTGTTGT | 5607 |
rs756061937 | in-del | -/CA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788971 | AGAGAGACCCTGTCT[-/CA]AAAAAAAAAAAAAAA | 5607 |
rs756068978 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590033 | ATTTTAGGCAGCTGT[A/G]TATTTTTTCCATATA | 5607 |
rs756089651 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765315 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 5607 |
rs756122864 | snp | A/G | 1.65913e-05 | 0.00288017 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693499 | TTATATTGTTCTAAC[A/G]GACTGTTTTGTCTCA | 5607 |
rs756130746 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789169 | CATTGAGGTCTTTCC[A/G]TATAATATAAAGATC | 5607 |
rs756133933 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637737 | GACTCTCAGTTTTGT[C/T]TTCTCATCTTAGGGA | 5607 |
rs756142453 | snp | C/T | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807368 | CGGATCTCAGGCCCC[C/T]GCCATGAGCTCCTTA | 5607 |
rs756148222 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751869 | ATTGATATTCTCGGG[-/C]CTCTTGAAGTGTATA | 5607 |
rs756154137 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67656304 | TCAAGCCATATATGT[C/G]ACGTCATGGGGAAAC | 5607 |
rs756154237 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673980 | CAGCCTTCCAAGTAG[A/C]TGGGAGTACACACAC | 5607 |
rs756177973 | snp | C/T | 0.000878087 | 0.020935 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600668 | ACCCTTTTTGTTTTT[C/T]TTTCTTTCTTGTGGA | 5607 |
rs756183760 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765360 | AGACTCCATCTAATA[-/C]AAATTTTTTTAAAAA | 5607 |
rs756192856 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736185 | TGGCAAGTGTAGCAG[A/G]GACCAGATAAAGAAA | 5607 |
rs756200890 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607429 | TGAACCTGAGCTCAT[A/G]GTTCTCTGTACCTTT | 5607 |
rs756246642 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693602 | AAATAATGTTTAAAA[A/C]CAACATCTTTATCTT | 5607 |
rs756272213 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666447 | ATGGGATCTTGATAG[A/G]CATGTTTCAGATGGA | 5607 |
rs756285788 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603840 | CAGCATGATTACATT[-/A]ATAGGCTATGCTACA | 5607 |
rs756299917 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600732 | TCTTGGTCATGGCAA[C/T]GGAGGCACAGTCTAC | 5607 |
rs756322444 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715861 | ATTTTCTGATGGATA[G/T]AACTCTACACTTTCC | 5607 |
rs756328777 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633017 | TTGTAGAACTGGAAG[A/T]GACCTTGGAGATCAC | 5607 |
rs756329698 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790949 | GAAGACGAGTCAGAG[C/G]TAGGGGGAATAAGCT | 5607 |
rs756406459 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67619204 | ACATGTAACCTGAAA[A/T]GAGAGGCATTTCCTG | 5607 |
rs756452146 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595130 | AATTCATATTAATCA[A/T]TAAAAGAAAGGGACA | 5607 |
rs756452981 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761312 | TTAAACTGGTGTAGT[G/T]TCTCCTTAAACCAGC | 5607 |
rs756459050 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571532 | GTCACCCTATTGTTG[C/T]GAACATGTTTCTTCT | 5607 |
rs756464035 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805191 | CCTCGCAGCTCTGAC[A/G]GTGCTCTGTGTGCCT | 5607 |
rs756464762 | snp | A/G | 1.65381e-05 | 0.00287555 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543516 | GCAAGGGGGACTCAG[A/G]GACTTGAGTAGTCAG | 5607 |
rs756464804 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586264 | CACATAAGCATATTG[C/T]ACATGGAATACCCTC | 5607 |
rs756468214 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582547 | CTTCCAGGCAGGGCA[C/T]AGTGGTTCATGCCTG | 5607 |
rs756468261 | snp | G/T | 1.66214e-05 | 0.00288278 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772683 | ACACAGATAACATAA[G/T]GGGTTTTTTTCTCTC | 5607 |
rs756479357 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628185 | TTTGTTGGTGGCATT[A/G]AAGAAGATACTGAAG | 5607 |
rs756482102 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581750 | AATTAACCAGTAGGC[C/T]CCTATTTGCACTGAT | 5607 |
rs756483769 | snp | A/C/T | 3.3082e-05 | 0.00406696 | synonymous-codon | MAP2K5 | GRCh38.p7 | 15:67769619 | TTCGCCCGTCCTTCC[A/C/T]GTTGGAGAGTTCTCG | 5607 |
rs756484055 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547376 | ATCTGTCAGATATTT[A/G]TCTGATTTATTGAAA | 5607 |
rs756495910 | in-del | -/AGG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643362 | AAGTGACTATTGATC[-/AGG]AGAAGTGTTTAAATG | 5607 |
rs756510979 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67679608 | GCGGTTTATCAGGCC[C/T]AGAGCATATCAGTTC | 5607 |
rs756517702 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67550047 | AGGATGTGATAGGCC[A/G]GGTTCTGCCTGAAGC | 5607 |
rs756523598 | in-del | -/TGTGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774168 | AGTGATGTGTGTGTA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs756528859 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566710 | ACTTTTTCCCCCTCT[G/T]GGATGCAGGCATTTT | 5607 |
rs756531953 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711999 | AAAACAATTGTTAAT[C/G]TACTGGAGTAAACAC | 5607 |
rs756544578 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705564 | ACATGGAGAAACCCT[A/G]TCTCAACTAAAAATA | 5607 |
rs756569307 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757594 | CTCGGTACCGGGGAT[A/T]GAGAATGAATAAGAT | 5607 |
rs756576343 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640384 | TTTATATTAAAGGGT[A/G]AAATGGAAGGTTAAG | 5607 |
rs756600471 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737406 | GGGACAGACCTGGCC[A/G]AGCTTTGTTTGAGCA | 5607 |
rs756610437 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780417 | ATTCAGTGCCTATCC[C/T]AGTCTGCTGTCATTT | 5607 |
rs756622201 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675982 | TAGTTATTTCCCCAG[-/T]CCCCACCTCTAAAAG | 5607 |
rs756622315 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689694 | CAGGTTCTTATTTAC[A/G]CCTTGTCTTTTGGAA | 5607 |
rs756632856 | snp | C/T | 4.95005e-05 | 0.00497471 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658595 | TGCCAGAACATGTCC[C/T]TGGAAGAATTGCAGT | 5607 |
rs756641270 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752418 | GGCACGGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 5607 |
rs756658224 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641548 | CTCACACTAATTTAA[A/G]TTGAGCACAGAGTAA | 5607 |
rs756659420 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67634764 | AAGTGTTAGCATGAT[-/A]TTTTTTTTTTTACTT | 5607 |
rs756666543 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676655 | TATTGAGTACCTTGT[A/G]TGTGCTACAGTGTTA | 5607 |
rs756686316 | in-del | -/ACACACACACAT/ACACACAT | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547103 | CACACACACACACAC[-/ACACACACACAT/ACACACAT]ACACAGATTTCTGTC | 5607 |
rs756708492 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627118 | GATGCCAGGTAATTA[G/T]TTTATTTTTTTTAAA | 5607 |
rs756719424 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765642 | CTGCCTGCTCTCAAG[C/G]TCACTAAACGTATTT | 5607 |
rs756720546 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574082 | AAATTCTTTCTGGCA[C/T]GACATCCAAGAACCA | 5607 |
rs756720904 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543037 | GGCAGAGACCTTCAC[C/T]ATAGCGTTCGCTCAA | 5607 |
rs756739333 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766685 | TCTTTCACATCCTGA[G/T]CAAAACTAACTTTGT | 5607 |
rs756747781 | snp | A/C | 1.65666e-05 | 0.00287802 | splice-acceptor-variant | MAP2K5 | GRCh38.p7 | 15:67769600 | TTTTTCCTCCATCAC[A/C]GGATTCGCCCGTCCT | 5607 |
rs756778676 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753864 | CTAGGTATATATCCA[A/G]GAGAATAGAAAACAT | 5607 |
rs756780199 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643772 | TGATAGAAACCACCT[-/A]ATGCCTTTTTTTTCC | 5607 |
rs756790356 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700729 | CCTTAAGAGTTGTTT[A/T]GGATAGACACGTGGA | 5607 |
rs756790780 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684500 | ACACTCTGGATTACA[A/G]TAAAATCCAGCATTC | 5607 |
rs756798955 | snp | A/C | 1.66804e-05 | 0.00288789 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646455 | GGATTTCAATATGTA[A/C]AGAATTCATGGATGG | 5607 |
rs756803617 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706757 | ACCAGTAAGTCATTA[A/G]AGAATAGTGTAAGGC | 5607 |
rs756804616 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558160 | CTCAAGCACCAGACT[A/G]GTTGTTCCTTAAGGT | 5607 |
rs756812137 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698344 | AGGCGTGCACCACCA[A/C]GCCCGGCTAATTTTT | 5607 |
rs756820453 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734759 | CCTTTGTTGCATAAA[C/G]TTTTTGAAGTTTGGA | 5607 |
rs756820509 | snp | A/G | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720212 | TTGGTTTAATGTAGT[A/G]TAGACAGATTAATAT | 5607 |
rs756825424 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777123 | GAGCTGACTGTAGGG[A/T]GGGAAGTGTTCACTC | 5607 |
rs756829687 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593539 | CTAATTTTGATTCAA[A/G]TAAATGGACACATCT | 5607 |
rs756834535 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674153 | TGCCCGGCCCCAAAC[A/C]CTTTTTTAAAAGAAC | 5607 |
rs756837007 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721521 | ATTTGCTGTGGCTCA[C/G]CCACTGCACTAGAAG | 5607 |
rs756842880 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544273 | GTATGACACATCATC[C/T]GTTATTAAAATGAGT | 5607 |
rs756858873 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729044 | TTAGTCTCACTTTTC[-/A]AATTCATAGACTTTT | 5607 |
rs756861124 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625805 | TCCACGGATGAATTA[A/G]CGTGCATCATAATTA | 5607 |
rs756950805 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805709 | CGCTATGGCTCCCCG[A/C]GTCTCACCATGCAAG | 5607 |
rs756956307 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598308 | ACATTATAGGAACAC[A/G]TTGCTCACTTTTTAT | 5607 |
rs756976714 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745227 | TGGACAAGTTAGTTA[C/T]AAACAGCATTTCATA | 5607 |
rs756978443 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693248 | ATCAGGCGGGTTTGG[G/T]ATACTAAAGCGATAA | 5607 |
rs756997104 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565480 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 5607 |
rs757015032 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67733569 | GGGTAAAAGGAAGGT[C/T]TGAATCTTTGGGATC | 5607 |
rs757017850 | in-del | -/GGCCACCC | 0.00010568 | 0.00726836 | frameshift-variant | MAP2K5 | GRCh38.p7 | 15:67806646 | TCCTCTTCCCCGCAG[-/GGCCACCC]GTTCATCGTGCAGTT | 5607 |
rs757022291 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785465 | TGGCACAGCTGTAGG[A/G]AATACAGAGGGCTAT | 5607 |
rs757033259 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773899 | GGAGACCCATTTACC[G/T]TGTGCATTATTATGC | 5607 |
rs757038308 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585869 | TGATGTGTTCTACAA[C/T]TTAGTCAATTACTGT | 5607 |
rs757041336 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603899 | TCCACTCATTGGTAA[C/T]AAAACTGCCTAATAG | 5607 |
rs757069169 | in-del | -/CAAA | 0.000186411 | 0.00965249 | intron-variant, frameshift-variant | MAP2K5 | GRCh38.p7 | 15:67670420 | ATATGTGTTTTTTAG[-/CAAA]CAAAGACCTGTGCAC | 5607 |
rs757085022 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579231 | CAAATAGCCACTGGC[A/G]TCTTAATTTTCCATG | 5607 |
rs757091372 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67551963 | AAAATATCCAACCAC[A/G]CTTCCCCAACTTTAT | 5607 |
rs757092462 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728675 | TCTGGCATCTTGGTC[G/T]GTACAGGCCAAAGTG | 5607 |
rs757097564 | snp | G/T | 1.65102e-05 | 0.00287312 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585978 | AGATGGATTTGTAAT[G/T]CTGTGTTCCACTTAT | 5607 |
rs757106725 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760535 | TTACTAACCAAAATA[G/T]TAACATAAACATCCC | 5607 |
rs757121831 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796400 | TCAGCTTCTGATAAG[A/G]CCTCAGGAAGTTTAA | 5607 |
rs757139555 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67695996 | AGTAGGAGGCTCTTA[C/T]TGGCCAAGTGCTCAC | 5607 |
rs757148081 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624592 | ATCACGATCTCTTTG[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 5607 |
rs757158122 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564125 | CTGGTAGAAAGAGCA[C/T]TGGACTGGAAGTCAG | 5607 |
rs757160018 | snp | C/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720027 | TGATGGAAATCAACA[C/T]GGAACGGTTAAAGTG | 5607 |
rs757175210 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625423 | TTCCTCCATGCAGTC[A/G]TTGAATCAGGTAATT | 5607 |
rs757179589 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582253 | TTTTAGCAGAGACAG[G/T]GTTTTACCATGTTGG | 5607 |
rs757194174 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703291 | GTGTATGTGTTTTCC[C/T]GAGTAGCATCCGTCC | 5607 |
rs757206778 | in-del | -/AATAATAATAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686625 | AATAATAATAATAAT[-/AATAATAATAA]TAATAATAACATGTT | 5607 |
rs757212688 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614354 | AGGTTTTCTGAAGTA[G/T]CCATTTATGTATCTG | 5607 |
rs757229046 | in-del | -/AGAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675043 | ACATTTAAAAAAAAG[-/AGAA]AGAAAGCTAGACATG | 5607 |
rs757229094 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67770392 | CGTCCTGCAGGACTC[-/AT]GTGGCCTTGGGAGGC | 5607 |
rs757251316 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657993 | AAAAAATATTTGTCA[A/T]ATACTCTGGAATACA | 5607 |
rs757258555 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705107 | AGCTTTCACACAGCA[A/G]CTCTAGAGTTGTGTG | 5607 |
rs757258744 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767764 | ATGCTATTTTGTGTC[G/T]TGTTTCTTTTGAGTG | 5607 |
rs757265634 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67644323 | GGCTTGAACCCGGGA[A/G]GCGGAGGTTGCAGTG | 5607 |
rs757277592 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617521 | CTCCTAGAATTTGAA[-/AT]TCTAGGCATAAATAA | 5607 |
rs757283250 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737455 | TTTAACAGTTATGGA[G/T]TAATGCGTGGGAGGT | 5607 |
rs757291083 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595330 | CTGGCCTGTGTTTTC[C/T]GATTAGTCTCTGCTC | 5607 |
rs757311940 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593612 | TACCTACAGGGTCCT[C/T]GATTCTTCAGTAGCA | 5607 |
rs757316987 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662682 | ACATAGAAGGTAGTA[C/G]TTGTCACCCATATAC | 5607 |
rs757318781 | snp | A/C | 0.000185753 | 0.00963545 | utr-variant-5-prime, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549158 | AGAAATGAGGTTTGC[A/C]GGCCATTGGAGTTGG | 5607 |
rs757334385 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631001 | TAGCTTGAGTCACAG[A/T]TATTGTCAAAGAGGA | 5607 |
rs757374650 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738959 | TATCAAAATATGGGA[G/T]GTGTGAAGTAAAACT | 5607 |
rs757383630 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561274 | TTGTTTTTTCCTGTC[G/T]CCTGCATTTTTAAGA | 5607 |
rs757395252 | snp | C/G | 1.66632e-05 | 0.0028864 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630881 | TTGTTTTTTTTTCTT[C/G]CCATAGAGCATATCA | 5607 |
rs757398096 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703423 | GGTACGTTGTTTGCA[C/T]ATAGACGCTTCTGTG | 5607 |
rs757412799 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554141 | CTCAGCTCACTGCAA[C/T]CTCTGCCTCCCAGAC | 5607 |
rs757456568 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703520 | TTCAGCATGTTATAT[A/G]GATGTATACAGAGTT | 5607 |
rs757475595 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690690 | AGGTGTCCGCCACCA[C/T]GCCCGGCTAATTTTT | 5607 |
rs757485087 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669378 | GTTGCGTATTAATCA[A/T]AGAAACCTCATAGGG | 5607 |
rs757490376 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793462 | TCATTTCTTGCTGCT[A/G]TTCTTGTTCCTCCCT | 5607 |
rs757492369 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67710209 | CATTTTGCTCTTTTC[A/T]CTTGGATCTTCATTC | 5607 |
rs757503534 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606770 | AAATTAGAAGGACTG[A/C]TGGTCATTTGTATAA | 5607 |
rs757536195 | snp | C/T | 0.000135492 | 0.00822969 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806599 | AAAGTACAATGAGCG[C/T]GGGAGTCCGAGGACT | 5607 |
rs757540949 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780635 | AATTAGGGTGGCCAC[A/G]CTAGAATACATGGCC | 5607 |
rs757542974 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607964 | TTTCAAGTAAGAATT[C/T]GCTGAATCTAAGTGT | 5607 |
rs757544925 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544372 | TTTTTCAGAATATAT[G/T]TCAAATAAAATGATG | 5607 |
rs757558902 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67573755 | TGATGTCCTGATATC[G/T]TAAGAACAAAAGCAT | 5607 |
rs757564528 | in-del | -/GT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784737 | AAAACTGAGGGCAGA[-/GT]GTGTCCTGACAGCTG | 5607 |
rs757589011 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747584 | GTTGATCAGAAATGC[A/G]CTCTTACTGGACTCT | 5607 |
rs757593426 | snp | A/G | 3.32491e-05 | 0.00407719 | missense, intron-variant | MAP2K5 | GRCh38.p7 | 15:67664597 | TTTTCCTAAATTTAG[A/G]TTGTTAAAGGCCTTA | 5607 |
rs757602167 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616696 | TCTTCTACCTGTTCT[C/T]TGAGAGACATAGGGA | 5607 |
rs757649753 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570182 | TTGGCTGCCCAAACT[C/T]CTATGAAGGCCATCT | 5607 |
rs757649865 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788090 | CTTGAAATTCTGCTG[A/G]TCTGAGGCAGCTTCC | 5607 |
rs757688643 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713126 | TTAGTATTCCTATAG[-/A]AAAAAAAATCATTTT | 5607 |
rs757698119 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574845 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 5607 |
rs757701600 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628324 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGCTGGT | 5607 |
rs757721883 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624088 | CTCACACCTGTAATC[A/C]CAGCACTTTGGGAGG | 5607 |
rs757729383 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642609 | CCCAAGTACAGGAAA[C/T]AGCAGGAGCAAAGGC | 5607 |
rs757742113 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682876 | TGGGTGCAGTGGCTC[A/G]TGCTTATAATCCCAG | 5607 |
rs757776560 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548859 | GGCTGTAATGAGCAA[A/G]GACTGCCTAAGATAG | 5607 |
rs757809014 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771619 | TACCAACTCCACTGG[C/T]GAGACAGCTTGAATT | 5607 |
rs757816048 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693921 | CAGTCAATAAAATTG[-/T]TTTTTTTTTTTCTTG | 5607 |
rs757816556 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663092 | TGTTTTTTCCTGAAA[C/T]ATTTGAGAATAAGTT | 5607 |
rs757819392 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582679 | ATACAAAAATTAGCC[C/G]GGCGTGGTGCACACT | 5607 |
rs757867914 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799727 | GATCTGCCCAGTGGG[C/T]CCACCCACCCAATGT | 5607 |
rs757873198 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756087 | CCTTTTCCTAGAGCT[A/G]TGGCTTGCCACAGTC | 5607 |
rs757874807 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678872 | AGGAGGCTGAGGCAG[A/G]AGAATTGCTTGCACC | 5607 |
rs757887512 | snp | C/G | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658575 | TTTGGATGTATATAG[C/G]AAAATGCCAGAACAT | 5607 |
rs757916602 | snp | C/G | 1.79107e-05 | 0.0029925 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646492 | TTCCCTTTTATAATA[C/G]TTTTAAAATGATTTT | 5607 |
rs757919468 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613517 | AAACACTGTAATGCA[A/G]GATGAAACTAGCCAT | 5607 |
rs757922524 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67544456 | TTTTTGCAGATAGTT[A/G]CTGAGGAGCAGTGAG | 5607 |
rs757930145 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774297 | ATATCAATAAATCAA[C/T]AAAATACAATGAAAA | 5607 |
rs757955923 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704872 | TATAGTGTAAGACAA[-/T]TGAGAAGTTACATGG | 5607 |
rs757958619 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579758 | AGCAATAGGAAGATA[C/T]ATGTGATATCTTCTA | 5607 |
rs757958965 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765794 | TGCTACTTGCCTTTT[C/T]TTATGCCTGAGTACC | 5607 |
rs757959619 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565532 | TGTGCCCGGCCTGTC[A/T]TCATCATTATTAAAT | 5607 |
rs757969715 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67585901 | TCAGCCTGCAAGCCT[C/T]CTGGGGAACGGAACA | 5607 |
rs757971945 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659936 | AGACTGTTGAAGTGA[A/G]TAGAGTCAGCAGAAA | 5607 |
rs757980201 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600646 | ACATTTCCATCCACA[C/G]CATGACACCCTTTTT | 5607 |
rs757992680 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687816 | TGTATGTACCAGACA[A/C]CATTCTAGATGTGGT | 5607 |
rs758009392 | in-del | -/AG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675828 | GATTTGATCATAGGC[-/AG]AGTCATCCCTTTTAG | 5607 |
rs758019068 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735894 | TAGGCTCTGTGGTCC[A/G]GGAGGCCTTCTACTT | 5607 |
rs758080561 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732590 | AGCAAATAGTGCCCC[-/T]GGTATTGTAAAGCTT | 5607 |
rs758104310 | snp | G/T | 1.65655e-05 | 0.00287793 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703300 | TTTTCCTGAGTAGCA[G/T]CCGTCCACTCACAGG | 5607 |
rs758111926 | in-del | -/GTTAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552819 | GAAAGTCTCTCAGCT[-/GTTAA]GTGGTAAAGTGGAAT | 5607 |
rs758124572 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67554036 | GAATAAATACAACTT[C/T]AATAAAAGAAATACT | 5607 |
rs758129359 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767229 | ATTTTGTTTCTCATC[C/T]GTTTTTAAATGGCCT | 5607 |
rs758138224 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600507 | AACTTTCCATCACTT[C/T]GTCCCTTGGTATCGT | 5607 |
rs758147394 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67689606 | AAACCAGATTGAGGG[A/G]AGAATATGGAAAAGT | 5607 |
rs758157671 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572956 | CTGCCTCGGCCTGCC[A/T]AAGTGCTGGGATTAC | 5607 |
rs758172332 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804143 | CAGTGCCGTCACGAC[C/T]CCCCGCCTGCCTGCC | 5607 |
rs758183100 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730108 | CAGAAGTTGGGGTGC[A/G]TCGTTGCTAGAACCA | 5607 |
rs758189587 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592421 | ATAAGTAACTTGTCC[C/T]AGATCACACAGCTAG | 5607 |
rs758190358 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616762 | GAATAAGACCATCTC[-/T]TTTTAATTACTGGTT | 5607 |
rs758191583 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67578288 | TGCTAAGAGGTACCA[G/T]GCATGGCCCTGCATT | 5607 |
rs758198030 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67761459 | AAGCAAATAAAGCCA[A/G]CACTCATACACGCAG | 5607 |
rs758212529 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727958 | CAGGTAAGATTGTTC[A/G]TTACTGCTGTTTGCC | 5607 |
rs758225577 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67717493 | ATGGAAACATGTAGA[A/G]CTGGGCACATGAGAG | 5607 |
rs758231627 | in-del | -/AACT | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721983 | AATAATAATAAAACA[-/AACT]AATTGTCTTTAATTA | 5607 |
rs758232214 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668188 | GCTAAGAATGTGGCA[C/T]GTTTTTATTATAACC | 5607 |
rs758237405 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785685 | AGCCATGACCTCGCT[C/T]ATCCTATGACCTTGA | 5607 |
rs758249822 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683033 | GTAATCTCAGAGACT[C/T]GGGAGGCTGAGGAAG | 5607 |
rs758280306 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647331 | CTTACAGCCATATAG[A/G]TAAGTATGGTAACTG | 5607 |
rs758298978 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552400 | GCATTCCATGGGTTA[C/T]CTTATTTCTTTTAAC | 5607 |
rs758325066 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774390 | TTTGATTTTAAATGA[A/G]TGCATTCCCAGAGGT | 5607 |
rs758329795 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620149 | GTTGAGGCGGGTAGA[C/T]CACCTGAGGTCAGGA | 5607 |
rs758351959 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645902 | CATTCCTATGCTCCT[C/T]TTTTGAAAATAGCCA | 5607 |
rs758359890 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596942 | TTTGGGAGGCCGAGT[C/T]GGGCGGATCACGAGG | 5607 |
rs758371955 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800187 | GCATCCTCCCATAAA[C/T]TATTTAACGTCTCTA | 5607 |
rs758388279 | in-del | -/CTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587072 | TGAATGTTTAGATTT[-/CTC]AGACTGGGTGCTGAG | 5607 |
rs758398379 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599201 | TTTTTTTCTGTATTA[A/G]TAGTATAAAGGTAGT | 5607 |
rs758411454 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584015 | CCACTTCTCCAAGTG[C/T]TGGGATGAAAGGCAT | 5607 |
rs758419759 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67713326 | ACATACACATATTGT[G/T]TAATGGATGCCAGAT | 5607 |
rs758426128 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765363 | ACTCCATCTAATAAA[A/T]TTTTTTTAAAAAGTA | 5607 |
rs758428118 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786585 | GCGGGAGCTCGGAAC[A/C]GTGGCCGAGGGGCCG | 5607 |
rs758428404 | in-del | -/AGG | 8.72791e-05 | 0.00660545 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806790 | CAGGACCAGTAACCA[-/AGG]AGAACAACCCACCCG | 5607 |
rs758428547 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566156 | TTTTTTGCAAAAAGC[-/T]GTTTTTTTCTTTTGT | 5607 |
rs758428929 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629079 | AAACCATGAAACCAA[G/T]GTGGCCATGGCGGTT | 5607 |
rs758435632 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696751 | GGGAGGCCAAGGCAG[C/G]CAGATCACCTGAGGT | 5607 |
rs758458793 | in-del | -/TCTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631421 | TCACTGTACTTTCGG[-/TCTTT]TCTTTTCCTATGCAC | 5607 |
rs758474567 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635994 | TTATAAATAAAGATG[C/G]GGTTTTGCCACATTG | 5607 |
rs758501897 | snp | G/T | | | utr-variant-5-prime, intron-variant | MAP2K5 | GRCh38.p7 | 15:67549032 | TAAGTGCCCTGCTTG[G/T]AAAGGCTGTGGGCTC | 5607 |
rs758536891 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67607266 | ATAGTATCGTGACAA[A/G]CAAGGATATTAATGT | 5607 |
rs758540601 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772537 | GAAATCTGACTAAGT[A/G]AAGACCAAAATAAAA | 5607 |
rs758545538 | snp | A/T | 1.65685e-05 | 0.00287819 | stop-gained, intron-variant | MAP2K5 | GRCh38.p7 | 15:67664619 | AAGGCCTTACTTATT[A/T]GTGGAGTTTAAAGAT | 5607 |
rs758547790 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725756 | GATACCTGTTAAGAC[A/G]CTGCAGACTGTTGCA | 5607 |
rs758572641 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691988 | TTAATTTCCTCATCG[A/G]TTTCATTCAAATATG | 5607 |
rs758592499 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562682 | GGAGACCTGTATTAG[A/G]GCTGCTTTACAAGTT | 5607 |
rs758602136 | snp | G/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67563307 | AAGATGGTGATCGAA[G/T]TACAGTGAGAAGTGA | 5607 |
rs758617154 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783434 | TGCTTGTGCTGTTTT[C/T]TCACCGCCAGATGGT | 5607 |
rs758625126 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782296 | TAATCGGGAGATTAG[A/G]GCCCCAGGGACAATG | 5607 |
rs758641324 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655885 | ATTTTACAGGTCTCC[G/T]AGAATGTGTTCATTT | 5607 |
rs758648436 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579733 | TTGTAATAATTTTAA[C/T]GTACATAAAAGCAAT | 5607 |
rs758650096 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794640 | GAACATCACAGCTGA[-/AA]AAAAAAAAAAAAAAA | 5607 |
rs758669570 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794639 | GGAACATCACAGCTG[A/G]AAAAAAAAAAAAAAA | 5607 |
rs758677553 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609327 | CTATCCAGAACTCAC[A/G]CTAGTGGGGCAAACA | 5607 |
rs758677609 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623337 | TCTAGAAGTTGGAAC[A/G]TGGTATATCCATACC | 5607 |
rs758684530 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595439 | ATTTGTGAAGCAAAG[G/T]TCTAGTGATGGGACT | 5607 |
rs758692986 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67734816 | AATATACAGTTTTTT[A/G]TATGTGAGGTCTTTA | 5607 |
rs758733805 | snp | C/T | 1.67066e-05 | 0.00289016 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67592944 | AAAGAAGTCTTCTGC[C/T]GAACTGAAAAAAATA | 5607 |
rs758734280 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571301 | TTAATACCTCTGGCA[G/T]AAGAGGAAATAAAAT | 5607 |
rs758747594 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603975 | CAAAGCAAAAGTTTA[A/G]TAATGCAGTCTTATT | 5607 |
rs758750915 | snp | A/G | 1.65504e-05 | 0.00287662 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692432 | TAAAGAACAAACGCT[A/G]TAGATACATGGAATT | 5607 |
rs758754423 | in-del | -/TTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696128 | AGAAAAGAGCTGAGC[-/TTT]TTTTTTTTTTTTTTT | 5607 |
rs758758536 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701932 | TTTGAATCCTGGCTC[C/T]GCTCCTGGACAGTGC | 5607 |
rs758768019 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759251 | ATTGCCTAATAATAC[C/T]TCCCAGAAATTCAAA | 5607 |
rs758770328 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701060 | AATATTTTGTATGTG[C/G]GTTCCACTTTTGTGT | 5607 |
rs758780295 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684443 | CAAAATGATTCAGCT[A/C]TCAGTGTTCAGCAGA | 5607 |
rs758782058 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652079 | GAGTGAGAGGATATC[G/T]CACTGTGGTTTTGAT | 5607 |
rs758787694 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558960 | GGAAGAAAGCAAAGA[A/G]GTAAGGAAGGAATCA | 5607 |
rs758787912 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778612 | TCTTAGAGAAGTCAC[A/G]AGGAAAGATGGAAAA | 5607 |
rs758789815 | in-del | -/CCTGTAGTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729650 | GCGTGGTGGCGGGCA[-/CCTGTAGTC]CCTGCTGAGGCAGGA | 5607 |
rs758818695 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67649920 | AATTGAATTGAATTT[C/T]TAGATCAACTTGGGG | 5607 |
rs758845395 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590604 | ATTACAGGCACATGC[C/T]GCCATGCCTGGCTAA | 5607 |
rs758923322 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626199 | GTTACTTGGATTTAC[A/G]TGGAATAAACTTACT | 5607 |
rs758939954 | in-del | -/CTTTC | 1.67691e-05 | 0.00289556 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630970 | TCTTGATGTTCACCT[-/CTTTC]CTTTCCTCTGTTAGC | 5607 |
rs758940036 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596287 | ATTTGCTGGGTGTGG[C/T]GGCCCATGCCCAGCT | 5607 |
rs758945457 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543377 | TCCTGCCATGGAGAA[C/T]CAGGTGCTGGTAATT | 5607 |
rs758950018 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725151 | TGGTACAGAGAGGCT[C/T]CCAGCTGACCAAACT | 5607 |
rs758953177 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759500 | GGGAGGTGGAGGTTC[C/T]GGTGAGCCAAGATCA | 5607 |
rs758956694 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665168 | ATTCAGGCGGGAGCC[A/G]CCGCGCCTGGCCAAA | 5607 |
rs758963256 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570483 | TGAGTTATTGAGGAG[G/T]CAGAGCCTGAAGCCA | 5607 |
rs758975875 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794639 | GGAACATCACAGCTG[-/AAA]AAAAAAAAAAAAAAA | 5607 |
rs758978927 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67789171 | TTGAGGTCTTTCCAT[A/G]TAATATAAAGATCAA | 5607 |
rs758978983 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650991 | AGGCCAAGGCAGGTG[C/G]ATCACTGGAGGTCAG | 5607 |
rs758994836 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67583604 | ATTTACATAATCGAC[A/G]TGTAGACATACTGGG | 5607 |
rs758996400 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747751 | CTTCAACTACATAAT[C/T]AAAGTTTTCCTCACA | 5607 |
rs758998645 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585214 | CAGGAGGCTTTTGTA[C/T]TTTTAACATTTGTTG | 5607 |
rs759001097 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67782578 | AGCATTCACAGGGAG[C/G]AGCTAATTGTCTATG | 5607 |
rs759017578 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678527 | ATATGAAACAAAGAC[C/G]AAAAGGAAGTAGAAG | 5607 |
rs759033514 | in-del | -/TG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768613 | CTTTGCAGGGCACTT[-/TG]TGTAGGGATGTCAGG | 5607 |
rs759049098 | in-del | -/C | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681026 | TTCTACAAAGCAGTA[-/C]GCTTTATAGTATATT | 5607 |
rs759050021 | in-del | -/ACTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629694 | CATTCCTATCCTAAC[-/ACTT]ACTTACCAGATGAGA | 5607 |
rs759059807 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67582490 | ATTGACATTATAGCT[C/T]TGCCATAGAAAACCC | 5607 |
rs759074427 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708190 | TAGCCAGGAATGGTG[A/G]TGTGTGCCTATAGTC | 5607 |
rs759112064 | in-del | -/AT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601930 | AGAACTTATGTTCAC[-/AT]GTTTGGATTGTTTTT | 5607 |
rs759117830 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663206 | AAAATCAGGAAACTA[A/G]TATCGATACAATACT | 5607 |
rs759140578 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629713 | TACCAGATGAGAGGA[A/G]GAGCCGTCTGATCTT | 5607 |
rs759140977 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682320 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 5607 |
rs759142254 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691079 | TGCTACAGAGACAGG[C/T]TCTACAGTTCACCCC | 5607 |
rs759149164 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546804 | GAGTGGTGGCTTAGG[C/T]CTGTAATGCCAACAC | 5607 |
rs759156509 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783093 | TGGAGAGAAGCCGAT[G/T]TGGGAATCACAGATG | 5607 |
rs759156890 | snp | C/T | 0.000186515 | 0.00965519 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67670398 | TTTTTGTGGTAGTTA[C/T]ATGGTTATATGTGTT | 5607 |
rs759157786 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725985 | AATCACACAAAACTT[C/T]GAAAGGGAGTTTGGC | 5607 |
rs759205113 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560200 | TTAGAGAGAAGTGCA[-/T]TTTTGCTTTACAGGT | 5607 |
rs759205220 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67705897 | GGAAGAGAGAGACCA[A/G]TGTGACTTGACTGGA | 5607 |
rs759213736 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67690428 | TGTAGTGAAAGTGGT[A/G]TATTTAAGGTTTAAT | 5607 |
rs759215365 | snp | C/T | 3.29995e-05 | 0.00406185 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692561 | CACTCAGGTATGTCT[C/T]TTTTCCTCCCAGTGT | 5607 |
rs759218707 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677564 | ATATAATGTGGTATT[C/T]CTTTGTTTTCTTTCC | 5607 |
rs759245457 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610132 | TGTTTGCCATTCACT[C/G]TCTGAATTTCCTAAC | 5607 |
rs759266128 | snp | A/G | 1.72606e-05 | 0.00293768 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592977 | AGCCAATGGCCAGGT[A/G]GGTATTATTATATAT | 5607 |
rs759275285 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765236 | TGGTGGCGCACGCCT[G/T]TAGTCCCAGCTACTC | 5607 |
rs759286677 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577279 | TTATGCTCATTTGGA[A/G]GAAACTGATGTTTAA | 5607 |
rs759287521 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594862 | TCAAAATGTCTCCTT[C/T]TAATTCCTTAATTCC | 5607 |
rs759309013 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769926 | ACTTCTTTAAGCACA[A/G]ATACTGTTGCCATCC | 5607 |
rs759310113 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543348 | GTAATGCTGTGGCTA[A/G]CCCTTGGCCCCTTTC | 5607 |
rs759321545 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642316 | ACTACTGTGAGTTAG[A/T]CCCTGTGTGGAGTGC | 5607 |
rs759345418 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67778916 | TACTAATGATGGTTA[A/T]TAAATTGTGAACTTG | 5607 |
rs759352462 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603312 | GCTACTATGTCAAAG[C/G]GACCATTCTTCTATA | 5607 |
rs759388752 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67557699 | AGTATAGGAAACAAC[C/T]ATAGCTGATAACTGG | 5607 |
rs759389112 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570816 | GACTGAGCTACATAT[A/G]ATAGGGTATGCTTGC | 5607 |
rs759408911 | snp | A/G | 1.65389e-05 | 0.00287562 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748646 | CTAAAGTCATTCCTA[A/G]TGGTGTGGAAAGCTT | 5607 |
rs759415756 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67564112 | CTTTTCCCGTGGCCT[-/G]GTAGAAAGAGCATTG | 5607 |
rs759415880 | snp | A/G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542634 | GCGCCGCGGGAGGCG[A/G/T]GTCCCGCTCGTCGGC | 5607 |
rs759424950 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596442 | AACAACAGGAAAACC[-/T]TTTTTGTATATAGAA | 5607 |
rs759435393 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787674 | AATTAAGAATAAGTA[A/G]GATTTCCCTGGGGCA | 5607 |
rs759455277 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602430 | CTTTTATTTGCTTCA[A/G]ATGGAATTTAAAAAT | 5607 |
rs759466384 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67663736 | TAAAATTAGCAGGGT[A/G]TGGTGGTGTGCACCT | 5607 |
rs759476665 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569787 | ATAGGAGGTTTGGAC[C/G]ACCAACATTTTGTCA | 5607 |
rs759483472 | snp | C/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543443 | GACAGTGCACTCCGG[C/G]CCGCAGTTACTCTTC | 5607 |
rs759483686 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800617 | ATTGTTCATATGAAT[C/T]GTTTATGGTAAATAT | 5607 |
rs759484438 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665614 | AATATCCTAGTGATT[C/G]CACATTTCTTCTGAA | 5607 |
rs759486649 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650250 | TTCTCTATATACAAG[A/T]TAATGCCATCTGCAA | 5607 |
rs759489154 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698947 | ACGTATTACTACTAT[G/T]ATTTATTATTACTCT | 5607 |
rs759504431 | in-del | -/ATAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704437 | TCTTTAAATAATATC[-/ATAG]ATAGAGTTGCAATCA | 5607 |
rs759579186 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700446 | AGCTGTCATGTGAGA[C/G]AGTAACCTCAGTTTT | 5607 |
rs759582270 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658524 | CTGGTAATTTCATTT[A/G]TAGTAACATGGCATG | 5607 |
rs759585470 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67617593 | TGCATGGCATAAATT[C/T]GTGTGGGAGTCCAGA | 5607 |
rs759589855 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773871 | GAGAAAACTTGGAAC[A/C]GGTTCTAGAGATGGA | 5607 |
rs759593730 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67568759 | CTCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 5607 |
rs759596919 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565965 | GAAATTTAAGGAGAA[A/C]CATTTGGACGTAACC | 5607 |
rs759608629 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709216 | TGGGCTCACTCTGTA[C/T]TGGGGAAGAGAACCC | 5607 |
rs759620697 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647112 | GTCTTTAAATTTTAC[A/T]TATTCAGTTTTCCAT | 5607 |
rs759635259 | snp | A/G | 8.24232e-05 | 0.0064191 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585943 | AAGGTACGAATTTCA[A/G]TAATTGTTTCAGTAA | 5607 |
rs759668940 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599003 | CTATTTGTGCCCACC[A/G]ATGGATACTGCTATT | 5607 |
rs759686658 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721208 | AAGTATTTATCTGTA[A/G]TGCTGTCTTTTCTCC | 5607 |
rs759686885 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67565355 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 5607 |
rs759689099 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580567 | CAGGGTGAAGGCTAA[C/G]ACACTGGACTTTCAA | 5607 |
rs759711320 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755574 | GGGAGCCATGTCCAA[A/G]TGAAGAGTCCATGTG | 5607 |
rs759712844 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618145 | TCTTTAACATTTCAA[A/G]GAGTAAATAATATAA | 5607 |
rs759725070 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600142 | GATTTCTGCCTAATT[A/G]TTGCTGTATACTAGT | 5607 |
rs759725302 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67586170 | GTTTTGTTGGTCAGT[A/G]TCTTCAGGATAATCC | 5607 |
rs759745096 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613263 | AAAAGACTGGCTTTG[C/G]TAAGGTATCTTGCAA | 5607 |
rs759757945 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640430 | TGATCTTTTCCTGAC[C/T]CTCTCCTGACTTTTG | 5607 |
rs759761661 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587984 | CCTCCTGAGAGTCTA[C/T]TCCCTCCGTTCTTGG | 5607 |
rs759773927 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654342 | ATTTTTTCCACTAGT[A/G]TAGTCACTGCAGCTC | 5607 |
rs759781589 | in-del | -/CTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67616099 | TCTTTGAAATGGAAA[-/CTT]CTAAGTTGAGGAAAG | 5607 |
rs759783448 | in-del | -/CT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641429 | TGACCTGTGATTTTG[-/CT]CTCTTTCCCTTTAGT | 5607 |
rs759813172 | in-del | -/GC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724318 | ACTTGGAGCATATGT[-/GC]TCCTTCTTCCCCATA | 5607 |
rs759833266 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659557 | AGTAGCTTCTCATCT[A/G]CATGTGCAGGTAGAT | 5607 |
rs759853910 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793957 | ACACATCCATAGTGA[A/C]TCTTATTGAATTAAA | 5607 |
rs759864055 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560919 | GCCCCCCCCTTTTTT[A/T]AAATAAATTATAAGA | 5607 |
rs759880856 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723704 | GATATGAGACCCATT[C/T]GATGAATTGCTGGCA | 5607 |
rs759893246 | snp | A/T | 1.65255e-05 | 0.00287445 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693590 | AAACTTATGCAAAAA[A/T]AATGTTTAAAACCAA | 5607 |
rs759895277 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751866 | GACATTGATATTCTC[A/G]GGCCTCTTGAAGTGT | 5607 |
rs759897303 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67608702 | ACAGCTGACTTAAAG[G/T]CTGAAGGGCATTTCT | 5607 |
rs759900314 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798049 | CCATCCTTCTGAGCA[C/T]TGTGTCTTTAAACCT | 5607 |
rs759932463 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763486 | CATTCTGTTACAGCA[C/G]ATATGTACATTGAGG | 5607 |
rs759944551 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600725 | GGGACACTCTTGGTC[A/G]TGGCAACGGAGGCAC | 5607 |
rs759979891 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781408 | ATTGTGAGTCTTGTG[C/G]TTTCGGATACAGAGT | 5607 |
rs759983588 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703386 | ATTCTGATGTCTGGA[A/G]CTTAGGAATCTCTTT | 5607 |
rs759992036 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574665 | CGAAGTAAAGAGATC[A/G]AGACCATTCTGGCCA | 5607 |
rs760004594 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766805 | GAGTGTTAACAGCTT[C/G]CATACTTCTGTGGAG | 5607 |
rs760020945 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704785 | TTTTGATTTGTGGGA[C/T]TCAGTATTGCTGTTA | 5607 |
rs760038604 | snp | G/T | 1.77407e-05 | 0.00297826 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642455 | GCAGAATGTACATAT[G/T]GAGGGCCAGAGCTAG | 5607 |
rs760041044 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67661441 | TATAAGTACTTTTAG[C/T]GTCAAGGCTTTGTCA | 5607 |
rs760050083 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788834 | AAAAACTAGTTGGAC[A/G]TGGTGGCACTGCCTG | 5607 |
rs760055976 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716771 | AGCTCTTGACATCCT[C/G]TTGCTCAGTGTCATT | 5607 |
rs760058176 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665842 | TAAGTGTGTAAACAA[A/C]TTTGGTGGATGAAAA | 5607 |
rs760067592 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67633984 | GGTTCCAGAACACCC[C/T]TCCTATAACTTAAAT | 5607 |
rs760075396 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620320 | AGGTTTCATTGAGCC[A/G]AGACTGCACCACTGC | 5607 |
rs760096969 | snp | C/T | 6.61255e-05 | 0.00574964 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692579 | TTCCTCCCAGTGTAC[C/T]GTTTTCTCTGCAACA | 5607 |
rs760099756 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67804595 | TGGAATGTGGAGGAA[C/T]GCCTCTACGCTCCCT | 5607 |
rs760109337 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603800 | CACCTTAATGGTGTT[A/G]ATGATAAAAAATATG | 5607 |
rs760121492 | in-del | -/CAGATAACATAAGGG | 1.66424e-05 | 0.0028846 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772671 | AATATACAAATGACA[-/CAGATAACATAAGGG]GTTTTTTTCTCTCCA | 5607 |
rs760140297 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683966 | TCCTACTATCACCCA[A/G]GCTGTCTGCACAGAA | 5607 |
rs760145008 | in-del | -/T | 4.95573e-05 | 0.00497757 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748631 | ATGTGCTTTCACTCC[-/T]TAAAGTCATTCCTAA | 5607 |
rs760150612 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67570974 | CTCTCCTGTTACAGA[C/T]GTATGGAAGAATAAT | 5607 |
rs760152922 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67714107 | TGGCAAACAAAATAG[G/T]CATATTCCCTTTCCT | 5607 |
rs760173595 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584857 | GCCCGCCACCATGCC[C/T]AGCTAATTTTTTGTA | 5607 |
rs760203077 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631487 | ATCACAGATCTGACC[A/G]TGTCTTGCTGACTGC | 5607 |
rs760241466 | in-del | -/CATA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600427 | TGAGCTATGTTGTAT[-/CATA]CATTCCATTTTGACA | 5607 |
rs760265926 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790355 | GGGTTCATTACACTT[C/G]TGAGTGTGAGGTCTT | 5607 |
rs760268316 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618635 | CTCCCATCTCCGTAA[C/T]TGGAAACTCTATTCT | 5607 |
rs760275752 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726044 | CATCTTGTGATGTTT[C/T]TGTTATGTACAGTGG | 5607 |
rs760284047 | snp | A/G | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67693566 | ACAAATGCTTATATG[A/G]CGGTAAGTAAACTTA | 5607 |
rs760284516 | in-del | -/TACG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756572 | TGTGTTGATAACACT[-/TACG]TACGATCTACTCCCT | 5607 |
rs760313971 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800697 | AAACTCAGAGCCATG[G/T]ACCACACTGTATCCC | 5607 |
rs760328832 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67625640 | CTCTAAGTAAATACC[A/G]TTTGGAAAGTTAAGG | 5607 |
rs760337605 | snp | G/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600704 | ATGAACAAGACATAC[G/T]ATATCGGGACACTCT | 5607 |
rs760337616 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549730 | ATTCCACAGCCTCCC[A/T]TAGAAGAAACCAAGT | 5607 |
rs760340425 | snp | A/C | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807160 | GGGTCTGTGACCCCC[A/C]CCAGGGCTGGGGGCA | 5607 |
rs760351560 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643508 | CTGGTGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 5607 |
rs760368375 | snp | A/C | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543356 | GTGGCTAGCCCTTGG[A/C]CCCTTTCCTGCCATG | 5607 |
rs760382571 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67664231 | AGGTGTGGTGGCTTA[C/T]GCCTGTAATCCTAGC | 5607 |
rs760385788 | in-del | -/ACACACAA/ACACACACACACAG/ACACACACACAG | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67547107 | CACACACACACACAC[lengthTooLong]AGATTTCTGTCTAAA | 5607 |
rs760386835 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692667 | AACAGAAACTCTGCA[A/T]CTTTTCCTCATCTGG | 5607 |
rs760399190 | snp | C/G | | | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67580781 | GTAATGGAACAGCAA[C/G]TAAATGGACAGTTAA | 5607 |
rs760411140 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758382 | AGATGGGGCACACGG[A/G]AAGAGAGGCATTTTC | 5607 |
rs760421609 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543452 | CTCCGGGCCGCAGTT[A/G]CTCTTCAGGGATGTG | 5607 |
rs760424846 | in-del | -/TTTAACTTTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637997 | TTTTTTAACTTTTAA[-/TTTAACTTTT]TTTAACTTTTTTTTA | 5607 |
rs760432575 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688595 | TATTTTCTAAATATA[A/G]TGAAATATACAACTT | 5607 |
rs760449280 | snp | A/G | 3.32546e-05 | 0.00407752 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769582 | GTGACTTTTGGTGAC[A/G]TGTTTTTCCTCCATC | 5607 |
rs760470621 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629909 | AATAATGTTCAGAAT[A/G]TCTAGTCCCCACAGT | 5607 |
rs760488006 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579189 | ACCGGCAAATTTCCC[A/G]TTAAAAAGAATACCT | 5607 |
rs760498570 | snp | A/G | 1.66305e-05 | 0.00288357 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646430 | TATGGAGCATTTTTT[A/G]TAGAAAACAGGATTT | 5607 |
rs760502512 | snp | A/T | 1.6649e-05 | 0.00288518 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769682 | AGCCCGTTTACAAAC[A/T]TGCCATGCCCTCAAT | 5607 |
rs760553072 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566243 | GCAGTAGCCTGATCT[C/T]GGCTCACTGCAACCT | 5607 |
rs760553556 | snp | G/T | 1.65181e-05 | 0.00287381 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658539 | GTAGTAACATGGCAT[G/T]TTTATCTCTACAGGG | 5607 |
rs760566063 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700323 | TCTTATTAAGAACAG[A/G]TCAGGGTTTTTTGTT | 5607 |
rs760576221 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599802 | ATTTTTAAGCATCTG[G/T]ACCAGTGTGTAGAAA | 5607 |
rs760590207 | in-del | -/TCAG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630236 | GAGCCCCTGTCTGAA[-/TCAG]TCAGTCACTCAATCA | 5607 |
rs760597488 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675187 | CATAGCCAAAAACTG[A/G]AAACAACTCAGATGT | 5607 |
rs760601306 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67701651 | TGGAAATATTTAGTG[A/G]CTGGAGCTAAGTGTA | 5607 |
rs760609956 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769120 | GTAAAAAAAAAAAAT[-/T]TGATCCAAATTATTC | 5607 |
rs760662304 | snp | A/G | 3.29766e-05 | 0.00406045 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585954 | TTCAATAATTGTTTC[A/G]GTAAAGTTAGATGGA | 5607 |
rs760692913 | in-del | -/AAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788972 | GAGAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 5607 |
rs760698889 | snp | A/G | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67541736 | TCGGCAGGGGTTGGG[A/G]GCTGGTGGGGGTGGT | 5607 |
rs760700160 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675008 | TGGTAGGAATGTAAA[A/G]TGATACAGCCCCACT | 5607 |
rs760703523 | in-del | -/TTCTTTTTTTCT/TTCTTTTTTTTTTTCTTTCT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67575889 | TGTCTCTGTTTTCTC[lengthTooLong]TTCTTTTTTTCTTTC | 5607 |
rs760748248 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696617 | GTGAAACAGGGAACA[C/T]GACATTATATGTAGC | 5607 |
rs760773879 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731009 | TGCTGATCAAATGAG[A/G]CTATGGATATGAAAC | 5607 |
rs760779720 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67601764 | ATCCCAGAACATCCC[C/T]TACTCATTGATGCAG | 5607 |
rs760796993 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669131 | ATTGAGCAACTATTT[A/G]TTTTATACCTACTAC | 5607 |
rs760804285 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753194 | ACACAAAAATTAACT[A/C]AAAAAATGGATCAAA | 5607 |
rs760824723 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67621951 | CATTTTGGGAGGCCA[A/G]GGTGGGTGGATCACC | 5607 |
rs760829864 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591668 | GCCACCGCGCCGGCC[C/T]CTTAACAGGCTTTAA | 5607 |
rs760831248 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587977 | GCCACAGCCTCCTGA[A/G]AGTCTACTCCCTCCG | 5607 |
rs760832398 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762227 | TGTAAATGAAATCCC[C/T]TCGGTATGAGACAAG | 5607 |
rs760832479 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67776198 | AGAAGACAGGTAGAA[C/T]CCCACCCCCACCCCC | 5607 |
rs760845114 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792028 | CAGGCAGAGGAGGGG[C/G]AGGGCCAGGTCTCTG | 5607 |
rs760848969 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763729 | CAGTTGTGTCATAAA[A/G]ATGCTACTCTAAGGC | 5607 |
rs760858556 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794457 | TGGAAAACATTGGTC[A/G]CTAATAGCAGAAACT | 5607 |
rs760861881 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718571 | GAGTTTGAGACCAGC[C/G]TGGCCAACATGATGA | 5607 |
rs760896804 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696459 | TAGCTGACCCTTTAC[C/T]GAAAAAGTTTGCCAG | 5607 |
rs760909607 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642450 | TCAAGGCAGAATGTA[C/T]ATATTGAGGGCCAGA | 5607 |
rs760918850 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588874 | AAGTTAGAGTGCAGT[A/G]GCACAATCACAGCTC | 5607 |
rs760921441 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682549 | TCTTAAGAGCTGTAG[A/G]TTGGCTGGATGTGGT | 5607 |
rs760921870 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738811 | CTGAAAAATGCTGGA[C/T]AGGATATTTCTATGG | 5607 |
rs760930026 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610163 | TATTAACCCAAGTTA[C/T]TTTTGGATGTAAGAT | 5607 |
rs760942492 | snp | G/T | 0.000150776 | 0.0086813 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630869 | TCCCAAATGATTTTG[G/T]TTTTTTTTCTTCCCA | 5607 |
rs760947044 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67647271 | TGTCATAAGGTGTAC[A/G]ACATGCTCTAAATTA | 5607 |
rs760948087 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615791 | TAAAAGGTGACATCT[A/G]GAGGGTTTTAAAATT | 5607 |
rs760960525 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783270 | ACAGCCAAGCACAGG[A/G]TAGAATGTGAGAATT | 5607 |
rs760961472 | in-del | -/CAACATCA | 0.000231589 | 0.0107583 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658782 | ATAGACCAGCCCACC[-/CAACATCA]CAACATAGTCACACG | 5607 |
rs760974066 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67556072 | ATTACAGGCATGAGC[C/T]ACCGTACCTGGCCAG | 5607 |
rs760983678 | snp | A/C | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548725 | TTCCTGTCAATAAAT[A/C]CTTTCTAACTATGAG | 5607 |
rs760985381 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67698307 | ATTCTCCTGCCTCAG[A/C]CTCCAGAGTAGCTGG | 5607 |
rs761020425 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719616 | ATGAAGTTTGTCTAC[A/G]AAATTGTGGGTAGAG | 5607 |
rs761049989 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67784117 | GTTAGAGCATTCTTT[C/G]ATCTAAGTTATCTCA | 5607 |
rs761055446 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805274 | GAGAAGGTTGGGGGC[A/G]GGCACTGCATCAGCC | 5607 |
rs761079672 | in-del | -/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609026 | TTGCTGGGTGACTCT[-/G]GGGAAGTGGTGAACT | 5607 |
rs761095927 | snp | A/G | 8.23784e-05 | 0.00641735 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727902 | AACTAGACAAATATT[A/G]TTTCCTTTCCCAGCT | 5607 |
rs761099132 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666048 | CTTTAAAAAATGGAC[A/G]TCTATCCATTTGACA | 5607 |
rs761102357 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655586 | TAATCAGCTCTTGTT[C/G]TTTTGAGGATTATTT | 5607 |
rs761104065 | in-del | -/TTGTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738231 | GTAATGAAGCTTGTC[-/TTGTT]TTGTTTTCTGTTCAG | 5607 |
rs761109799 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740383 | TTCCATGTCCCATCC[C/T]CCCACTCTATCCAGC | 5607 |
rs761117212 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67576419 | ACAAAGCAAAAAATT[A/G]TACTTGTTATCCCCT | 5607 |
rs761146845 | snp | A/G | 5.31533e-05 | 0.00515498 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642463 | TACATATTGAGGGCC[A/G]GAGCTAGAGATGAAT | 5607 |
rs761158173 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691314 | GGCTGATAATATTTA[A/G]CAGGCTAAATGAGCT | 5607 |
rs761161583 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779324 | GCATATAATTACATC[A/G]GCAGAATCACTGTCT | 5607 |
rs761173550 | snp | G/T | 1.69628e-05 | 0.00291224 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772800 | TCAGTTATATATTTA[G/T]GTTTAACATTCTGTT | 5607 |
rs761180901 | snp | A/C | 1.66018e-05 | 0.00288108 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563369 | AGTATACGACAAATG[A/C]AGACTATTTTTTAAA | 5607 |
rs761188230 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652826 | CCCCTGGCAAACAGC[A/C]TTATACTCTGTCTCT | 5607 |
rs761196781 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704987 | GAAGCCACTGTTCTT[C/T]ACTGGGCCTCAGTTT | 5607 |
rs761196925 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574738 | TGGGCGTGGTGTCGG[G/T]CGCCTGTAGTCCCAG | 5607 |
rs761280984 | in-del | -/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762045 | TTACCTTTAGACCAG[-/C]CTGAGCAGGAGACTT | 5607 |
rs761290293 | snp | C/T | 9.89364e-05 | 0.00703267 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543479 | TGTGCTGGTGAGTGG[C/T]AATCTCAGTGTCCGG | 5607 |
rs761307065 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764822 | GAATATTTTTTTAAG[C/G]AAAAGGCCCTTAACT | 5607 |
rs761332453 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67764239 | TGCCAGTATGCATAA[A/G]GTTTGAAGGAATGTC | 5607 |
rs761347617 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627430 | TATAATTAATTGATA[C/T]AATAAAAGTTAAGTT | 5607 |
rs761353608 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602527 | AAGGTCTATTGTGAA[-/T]TTATTTTCCTAGCTT | 5607 |
rs761370313 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552151 | TGAACATTTTTCAAC[A/G]ATCATTGCCTGTTTT | 5607 |
rs761382322 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620794 | TTTGTTAAGTCAGGT[A/G]TGATTGTTAAAAATT | 5607 |
rs761383894 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558888 | TTTTCACTGTTACTG[A/T]CCCAGTGCCCAGAAC | 5607 |
rs761392703 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716307 | GATCATGCCATTGCA[C/G]TCCAGCAACCGAGCA | 5607 |
rs761438470 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627915 | TCATTGGAGGGCTGA[A/G]CTTTGAAACAACCGA | 5607 |
rs761445090 | snp | G/T | 1.67237e-05 | 0.00289164 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67600801 | TTTCCAAATACTGAG[G/T]ATCCAAGTTCTCTGT | 5607 |
rs761471992 | snp | A/G | 1.67849e-05 | 0.00289692 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769707 | CTCAATGTAAATGAT[A/G]CATGCCATTAACTCG | 5607 |
rs761473144 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655542 | TTCAAATGTCATTCC[C/T]CTGCCTCTGACCTCT | 5607 |
rs761498129 | snp | A/T | 1.64939e-05 | 0.0028717 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549997 | TTAGCAATAAAGAAG[A/T]TGGCTAATTGTGTTT | 5607 |
rs761511032 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769415 | CATTGTAAAATATGT[G/T]TGGCTTTAAATTTGG | 5607 |
rs761528078 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67802172 | CAGTGGAACATGTGG[C/T]CAGGAATTAGGGACG | 5607 |
rs761532123 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657583 | CTTCCCAGTAGCACC[A/G]AGAGCCAAAGTGTAA | 5607 |
rs761539183 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651870 | CTTTCTTTTGGATAT[A/G]TACCCAATGGTGAAA | 5607 |
rs761545847 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67786478 | GTTCAGAAAGAATAT[A/T]AGAAAGACCTATGTC | 5607 |
rs761548743 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613446 | CATGTGAAAGACCAG[A/C]TGTTTGGGATATATC | 5607 |
rs761566264 | snp | A/T | 0.000129374 | 0.0080418 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658800 | CATCACAACATAGTC[A/T]CACGCTTATGTGCTC | 5607 |
rs761566976 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666966 | TCCTGTGGTAATACA[C/T]CTCATTAAATATATT | 5607 |
rs761576538 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67711220 | TTTCCTACTTTTGTA[A/G]TGGTTTTTTTAAAGC | 5607 |
rs761579869 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737097 | AAGGCATCCAGAGAC[A/T]GTGAGTCTAAATGGC | 5607 |
rs761580637 | in-del | -/AG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67787599 | TTATTAATCATAAGA[-/AG]AGTTATTTAAAATTG | 5607 |
rs761594091 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67755978 | CATTGTCCTCCCCAC[A/G]TCCTCACTGTGGCAT | 5607 |
rs761604391 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67614428 | GCAAAGATTAGATGG[A/T]TATCACGTTGTTTCA | 5607 |
rs761614137 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743650 | TTGTTTTTCTCATTG[A/G]AGGCTTTCTGAGATA | 5607 |
rs761614249 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67756971 | TGGGTTGTCTTCCTA[G/T]CTTGGCTATTGTGAA | 5607 |
rs761616134 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790437 | CTTTTCATATCACAC[A/G]CTAATAAACTGTATT | 5607 |
rs761631893 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639643 | TCTTCAGAGGCTTCA[C/T]GTCACTTCCCAGATA | 5607 |
rs761637544 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580934 | GTTTAGCTCTTAATT[C/T]GAAAAACAAAAGAAG | 5607 |
rs761666101 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658567 | GGGGGATCTTTGGAT[A/G]TATATAGGAAAATGC | 5607 |
rs761677108 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723679 | CTGCTCCCCTCCTGG[C/G]AATGAAAAGGATATG | 5607 |
rs761690724 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566102 | GGATTTCGTATAAAG[A/G]CATAGGGAAGATACT | 5607 |
rs761702013 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586863 | GAATACTCGGGCCGG[A/G]CCCTCTCAACACAGC | 5607 |
rs761704816 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675477 | TTTACAATGGAGCAA[A/G]ATGAGGAATCCTCAT | 5607 |
rs761716596 | snp | G/T | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807266 | AGCTCCTCGCAGTTG[G/T]GCTGAGGCCCACAGC | 5607 |
rs761733080 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569079 | GTTTTGTCCTTACCT[A/G]CAAGGCTGTGTTTTA | 5607 |
rs761748312 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806195 | TGTAGACAAAGGAGA[A/G]AGCTAAAAGGGATTG | 5607 |
rs761753493 | snp | G/T | 5.13158e-05 | 0.0050651 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592888 | GGTGTTCAGAGGTGT[G/T]GATGATCTTGCCACT | 5607 |
rs761768890 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67574821 | GCACTGAGCCGAGAT[C/T]GTACCGCTGCACTCC | 5607 |
rs761774174 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560537 | TAGAATGCCTCTTTC[A/T]ACTTATCTGAAATCT | 5607 |
rs761784259 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572725 | TTTTTTTTGAGATGG[A/T]GTCTTGCTCTGTTGC | 5607 |
rs761789126 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694556 | AATCAAAACCACAAT[A/G]AGATACCATCTCACA | 5607 |
rs761797752 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640791 | TAGACTTCTGAGGTA[A/G]GAATATATTACAAGA | 5607 |
rs761798010 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722775 | TTTCTATAAAATGAA[A/G]ATTTAACTGCAGCGC | 5607 |
rs761800879 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67688678 | TGGACAGTTTAAAAA[G/T]CAATTTTACATTCAT | 5607 |
rs761811046 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676095 | ATTAGGGTAAGCTTC[C/T]ATCCAACCACCCAGC | 5607 |
rs761857722 | snp | G/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719820 | CATTCATTTTTCAAT[G/T]AGAAAAGTAAAATGG | 5607 |
rs761860272 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768217 | CTTGTAATTACCGAT[C/T]TCATTTTTCTGATAA | 5607 |
rs761874479 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67640917 | CATTTTGAAAATGAT[G/T]CTAATCACATTTTAA | 5607 |
rs761884232 | in-del | -/CTT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702131 | ATAGCTATTACTATC[-/CTT]CTTTTATAGTGGATA | 5607 |
rs761893071 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67624532 | CCTTTGTAAGTTTTG[A/T]ATTATATGTTTCCCT | 5607 |
rs761898141 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593023 | ATAATAACATATTAC[C/T]GTCCAGTTTTTGTAT | 5607 |
rs761912735 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783362 | CCTGTGGAGTCCTGT[A/G]CTCCAAACTTCTGGC | 5607 |
rs761930351 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683808 | ACTTCTACTTCTGCC[C/T]ATGGAGTCACTGCTG | 5607 |
rs761939087 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623245 | CTGAGATTAACACCT[C/G]AATGGCGTACTTACC | 5607 |
rs761942626 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67670777 | CTACAATGCCAGAAA[C/G]AGAGAGACAGGGTCA | 5607 |
rs761942685 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67669307 | CGGAGTGTGTTAGAG[A/G]GTTGTTAATAATAGA | 5607 |
rs761960287 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67610293 | GACAGTTATGACAAC[A/G]TAACTTGTTATTTGG | 5607 |
rs761982464 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732813 | CGGAGGCCAAAACTG[C/T]CATTTAGGGTTCCTG | 5607 |
rs761997219 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696748 | TTTGGGAGGCCAAGG[C/G]AGGCAGATCACCTGA | 5607 |
rs761997504 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588235 | CAGCTTTGCTGATGA[A/G]CACATAGTGCCCTGA | 5607 |
rs761998228 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753224 | AGACTTAAATGTAAG[A/C]GTAAAAACTACAAAA | 5607 |
rs762014102 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630326 | TTCTCATTCTTTTTC[A/G]TAAATGGATACATTT | 5607 |
rs762017531 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706350 | AAACAGACTCATTGA[A/T]TTTTCAGGATCGAAG | 5607 |
rs762050962 | snp | A/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67726266 | TCACTTTACGAGGTC[A/G/T]TAATGTTTATTCCTG | 5607 |
rs762060879 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597646 | AAGTCGAATTAATAT[A/C]CTTATCTAAATGAAA | 5607 |
rs762079821 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | MAP2K5 | GRCh38.p7 | 15:67748249 | CAGAAAAACCAGGGA[C/T]CTTTAATGGTAAGCT | 5607 |
rs762095046 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67645132 | AGCCGAGATCATGCC[A/G]CTGCACTCCAGCCTG | 5607 |
rs762118913 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559056 | GCCTCTGGTCCTGCC[C/T]ACGTCATTAACTCCG | 5607 |
rs762133150 | snp | C/T | 8.41149e-05 | 0.00648463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646222 | ATATTAATACCTTTC[C/T]ATATTTAGGTCATAC | 5607 |
rs762143615 | in-del | -/T | 1.69908e-05 | 0.00291463 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630863 | AGTGATCCCAAATGA[-/T]TTTTGTTTTTTTTTC | 5607 |
rs762145785 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777544 | CTGTGGTAAAAGTAC[A/G]TATCACATACATATT | 5607 |
rs762176003 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763928 | GTAGACATTGTTGGG[C/T]CAGGGCAAAGGAACG | 5607 |
rs762194105 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67795770 | TTCGTGGCTGTACTA[A/C]TTTCCTACCTGCATT | 5607 |
rs762195638 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584920 | CCAGGTTGGTCTTGA[C/T]CTCTTGACCTCATGA | 5607 |
rs762219919 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67637317 | TGACTAATACAGAGA[G/T]GGTATTTAGTTACTT | 5607 |
rs762222155 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609941 | GGTGTAGAGATGGAC[A/G]GGGCTTGATCATGCT | 5607 |
rs762224618 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558832 | CTCTTTCCACTAGAG[-/T]TGTATGTTCCATGAA | 5607 |
rs762248435 | snp | C/T | 1.86083e-05 | 0.00305021 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806826 | CCCTTCTCCGTATGC[C/T]GCCTGCGCCAGAAGA | 5607 |
rs762256432 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67631919 | TTGCCTTGCCCCCAA[C/T]CTTCCCCACAAATTG | 5607 |
rs762268601 | snp | C/T | 1.75345e-05 | 0.0029609 | missense | MAP2K5 | GRCh38.p7 | 15:67806727 | GCGCTGGAGGAGAGG[C/T]GGAGCCAGCAGGGGC | 5607 |
rs762277102 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657230 | TTTAGTTAATTAGGC[C/T]CTGATTTATATCCTT | 5607 |
rs762288813 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747406 | ATTTTCATTGAGTTT[A/G]TAATAACTGTAAGCT | 5607 |
rs762291862 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611332 | CCGAGTTAAGTTTGT[A/G]TACACCATTTGTTTC | 5607 |
rs762295231 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727640 | TGTGAATAATGCCCA[C/T]ATAGCTGAGAATATT | 5607 |
rs762311533 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67653290 | TCTGTTTAAAATATT[-/T]TTTTTTTTTTTTGAG | 5607 |
rs762332968 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67641218 | AGCATTGTATATTGC[A/G]TGTGCCAATTATCAT | 5607 |
rs762347295 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67736985 | TTAAATGACTCACTC[A/T]TGATTACCAGGTATT | 5607 |
rs762347555 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563245 | TGTGCATTAAACAAA[G/T]GCACACCTTATCATT | 5607 |
rs762361161 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67643691 | GACCTCGTGATCTGC[C/T]CGCCTCAGCCTCCTC | 5607 |
rs762370227 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754348 | TGGATAGGATGGGCT[G/T]CAGCAGAAGAAAAGA | 5607 |
rs762393711 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748106 | GTATTTTCATTATGT[-/AA]ATTGTGTTAACACAT | 5607 |
rs762402140 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67801295 | ATCACCATTTACAGG[A/G]CAGTCACCTGATCAC | 5607 |
rs762420561 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67737343 | ATTCAGTATGGAAAA[C/G]TTGGGTAGATTTGGG | 5607 |
rs762427338 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687759 | TCACCTGTTTAGTAG[A/G]GACACCATTTATTCA | 5607 |
rs762429021 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67723981 | TTTAATTAAGAAAAT[A/G]CAGTGCAACTCATAA | 5607 |
rs762440499 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67560814 | TATTTTGGTTTAAGT[A/C]GCCTTAAAGGTTCAA | 5607 |
rs762442173 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596785 | ATGTAATTGTAACTC[C/T]TGTGGCTTTTTCTTC | 5607 |
rs762449422 | in-del | -/AC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67771149 | TGTACCATGTGTTTT[-/AC]ACATGGTAATGTGTA | 5607 |
rs762479846 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603527 | AGATTTCTTATAAAA[A/G]GAAATTTCATTTACC | 5607 |
rs762487827 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67546594 | CTCAAAGGTAGAGAC[A/C]TTTGGGTCTTCTGTT | 5607 |
rs762488622 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780863 | GACAGAGCTAGGAGG[A/T]GCTGACCAGGTGGTG | 5607 |
rs762495871 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676232 | AGGGAGAGAGAGAGC[A/G]CCTGTATGATGAATG | 5607 |
rs762506312 | snp | A/G | 1.6612e-05 | 0.00288196 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67563250 | ATTAAACAAATGCAC[A/G]CCTTATCATTTGCAT | 5607 |
rs762529426 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67593113 | GGCTTAATTTGATTG[A/G]CAGAACAATTTGCAG | 5607 |
rs762531151 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569598 | AAGTGTAGTGACCCC[-/T]TTTAGCCCCTGTTGT | 5607 |
rs762553316 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67750817 | AGTTGGGATTTGAGC[C/T]GTTTTACTGCTTGGG | 5607 |
rs762580081 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67594466 | AAATTAAGAAGCTTT[A/G]ACTACATTTGTCCAG | 5607 |
rs762609485 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67678113 | GAACGTCAGCATAGT[C/T]TATACTTAATTGTAC | 5607 |
rs762611923 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67703139 | GATTCAGTAAGAATA[C/T]ATCTATATATAATTT | 5607 |
rs762614259 | snp | C/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67663520 | GCCTTTCTGACTCCT[C/G]ATGGGAAAAGCAGTT | 5607 |
rs762618050 | snp | C/T | 0.000139072 | 0.00833768 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658820 | CTTATGTGCTCCAAC[C/T]TGTTCTAGTTTCATG | 5607 |
rs762634320 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67791525 | CATGAACTAATGTAA[A/G]TGAAAGCACCTAGTG | 5607 |
rs762643208 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758008 | GTTTGGGCAAGTATT[A/G]TGAGATATAAACCAA | 5607 |
rs762647820 | snp | C/T | 5.44006e-05 | 0.0052151 | missense | MAP2K5 | GRCh38.p7 | 15:67806709 | TCCATGTGGGTGTGC[C/T]GGGCGCTGGAGGAGA | 5607 |
rs762661274 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67747075 | TGGAAGGAAAGGAGC[C/T]CTGGAGGAGCCCCAG | 5607 |
rs762661965 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67668837 | AAAAAAAAAACCTAT[A/G]TAGTTGGTGTGCCAG | 5607 |
rs762673194 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67586868 | CTCGGGCCGGACCCT[C/T]TCAACACAGCAGCCC | 5607 |
rs762688229 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615065 | TGCAATGGTGTGATC[-/T]TGGCTCACTGTAACC | 5607 |
rs762692403 | in-del | -/TGTG | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774174 | GTGTGTGTATGTGTG[-/TGTG]TGTGTGTGTGTGTGT | 5607 |
rs762714698 | snp | A/C | 1.69755e-05 | 0.00291332 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592905 | ATGATCTTGCCACTA[A/C]AAATTATCTTTCCTT | 5607 |
rs762715268 | in-del | -/AATAAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686619 | AATAATAATAATAAT[-/AATAAT]AATAATAATAATAAT | 5607 |
rs762730154 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606715 | TGTTTGGGAGCTGGA[A/G]TCATATTAGCTCATT | 5607 |
rs762735584 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67559630 | GGTATCTTGCTAGGA[-/T]TTTTTTCCTCCATTT | 5607 |
rs762740172 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67602096 | TCCAATGTGTCTAAT[A/G]ATTTTTGCGGCTACT | 5607 |
rs762749902 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67654124 | TTTGAAAGTGAGATA[C/T]TGAAGTCTCAAAAAC | 5607 |
rs762754006 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67780179 | CTCAACACTAGCAGC[C/T]CATCAGAGTTACCTC | 5607 |
rs762763260 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67684914 | CATTTCTACTACTAG[-/A]AAAAATATTTTTTTA | 5607 |
rs762797771 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745244 | AACAGCATTTCATAT[A/G]TTGTGAGGTGCAGGC | 5607 |
rs762836970 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788700 | TTAAAAATTTGGCCA[A/G]ACATGGTGGATCATG | 5607 |
rs762854416 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67798228 | CTCCTCTGGCATCCT[C/G]CCTCCTGATCCCTCT | 5607 |
rs762859444 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67555828 | TCACTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 5607 |
rs762868322 | in-del | -/A | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579698 | TTTATTTTCAAGAGG[-/A]AAAAAAAAAACCCTT | 5607 |
rs762882093 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67725017 | AGTCCTCCCAGGAAC[A/G]TAGTTAAAAGGTAGG | 5607 |
rs762919774 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757320 | CATTTGCAAATCAGA[C/T]TATGTCTTCCCATTG | 5607 |
rs762920762 | in-del | -/CAA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67788971 | AGAGAGACCCTGTCT[-/CAA]AAAAAAAAAAAAAAA | 5607 |
rs762929398 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642153 | ATTTTAGGTCAGTGT[A/G]GCATTTTTATTTGTT | 5607 |
rs762958922 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729284 | TCAGCTTGGCCAATT[-/T]GTGAAATCCCCTAAA | 5607 |
rs762959964 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662392 | ATTTACTTCTCATGG[A/G]TAATGATAGGTTTTC | 5607 |
rs762961900 | snp | C/T | 1.6486e-05 | 0.00287102 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543332 | TGAGCCTCTTTAACC[C/T]GTAATGCTGTGGCTA | 5607 |
rs762971054 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785188 | GACCTCAAGTGATCC[G/T]CCTGCCTGGGCCTCT | 5607 |
rs762988546 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67757343 | TCCCATTGATTCAAT[A/T]GTTGATGTTCACACA | 5607 |
rs762995710 | snp | C/T | 1.65196e-05 | 0.00287394 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748631 | TATGTGCTTTCACTC[C/T]TAAAGTCATTCCTAA | 5607 |
rs763007529 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67712671 | AGCCTGTAATCCCAA[A/C]ACTTTAGGAGGCCGA | 5607 |
rs763020603 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579110 | GTAATTTTTTTGACA[A/G]CCACTGATTGGAAAG | 5607 |
rs763036401 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543780 | TAGAAGAGAGGTTTT[C/T]TCCCCCCAAGTGTTT | 5607 |
rs763043246 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67744311 | AAGCTAGAATGTGAT[A/G]CCAGTAGCACAACAA | 5607 |
rs763061601 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67708867 | TTTAATATCAGACTA[C/T]CTTTTATCCAGGGAC | 5607 |
rs763064646 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797182 | CTTACATGTTATCAC[A/G]GTCCAGAATTTCATT | 5607 |
rs763067043 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638172 | TATTTTGTCACCCAG[A/G]TATTAAGCCTAGTAC | 5607 |
rs763077003 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67611464 | TCCTTTGGAGTCTCA[A/G]GTGAAATGTTTCAAA | 5607 |
rs763094965 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67721231 | TTTTCTCCCTTATTA[C/T]TAATAATCTGGGACA | 5607 |
rs763095793 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657666 | AGCAAAGTTTAACTA[A/C]GAGTGATCATTTTTC | 5607 |
rs763099018 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67577686 | AGTATATAGAAATGA[C/T]ACTAATAGATCCAGA | 5607 |
rs763106975 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67591390 | ATTATTATTATTATT[A/C]TTGAGATGGAGTCTC | 5607 |
rs763125833 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67597784 | TTTTTGTAATCAATT[A/C]TTGGGCTCTGCTTTG | 5607 |
rs763126355 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753592 | AAGCACATGAAAATA[G/T]GCTCAACAATTAATT | 5607 |
rs763128151 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67742278 | AGCAAAGACAGAATA[A/C]CTATATGTTTGGAAT | 5607 |
rs763135007 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693011 | ATAGTGACCCATGAG[C/G]ATGCTGTGATGTTGA | 5607 |
rs763188807 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722377 | TTTTTGGTCCTGCAT[G/T]ACTAAATCCTCCACA | 5607 |
rs763191987 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585986 | TTGTAATGCTGTGTT[A/C]CACTTATTGAAATGT | 5607 |
rs763206236 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67715587 | GACTGATTTTAAAGT[G/T]TTTCCAACAGCACAT | 5607 |
rs763206426 | in-del | -/TGAT | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67704110 | TTTTTAATAAAATGA[-/TGAT]TGATCTACAAAAAAA | 5607 |
rs763229142 | snp | A/G | 5.01668e-05 | 0.00500808 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646399 | ACAGTGCGATTCATC[A/G]TATATCATTGGATTT | 5607 |
rs763229251 | snp | A/G | 1.65023e-05 | 0.00287244 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580728 | CATACATTACTGAGT[A/G]ATCTCTTTCTATAAT | 5607 |
rs763242002 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67674895 | ATGCAAATTAAAACC[A/G]CCATGAGATATTACT | 5607 |
rs763252752 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67572264 | GGGAGAGGGTGGGAG[A/T]TGGGGCTTGGAGGAA | 5607 |
rs763253894 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67687290 | CAATAAGTCTGGAGT[A/T]GAACACAAAAAGCTG | 5607 |
rs763272823 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67766355 | GTGAGGTATGGCACC[C/G]AAGGTCTTAAAGAGA | 5607 |
rs763282321 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67580851 | AAATTCTAATCAACA[A/G]TGATTATTTCAGTAA | 5607 |
rs763292196 | snp | A/T | 1.87085e-05 | 0.00305842 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806836 | TATGCTGCCTGCGCC[A/T]GAAGAGCTTTGCTGG | 5607 |
rs763321932 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749879 | GTTTTGCTTGAGGAA[A/G]TGTCTGGGGAAACTT | 5607 |
rs763323468 | in-del | -/AC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765761 | AGTGTGCAGGTACAG[-/AC]ACACACACACATTTT | 5607 |
rs763326851 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67803302 | CATCTTTAAGAGTCT[C/G]GCCTTGCCAAGATGC | 5607 |
rs763328595 | snp | A/C | | | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67682380 | AGGCACACGCCACCA[A/C]ACCCAGCTAATTTTT | 5607 |
rs763330030 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796011 | TATTTTTTGTTGATA[C/T]TAATATAGCTATGCC | 5607 |
rs763333700 | snp | C/T | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807120 | CTTTGTGACAGCCTC[C/T]GCCATAAGAGTTGTG | 5607 |
rs763350918 | snp | A/C | 1.654e-05 | 0.00287571 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67692585 | CCAGTGTACTGTTTT[A/C]TCTGCAACAACCCCT | 5607 |
rs763357929 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67694016 | GATCTCTGAATGTAA[A/G]GGTTTAGGGGGCAGT | 5607 |
rs763358569 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67667421 | GCTTTCTCTAAATGA[A/G]TGATGATGGGAATTC | 5607 |
rs763367322 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67615812 | TTTTAAAATTAATCT[C/T]GCAAGGTACTAAAAG | 5607 |
rs763371920 | in-del | ATGTGAAGAAT/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67592807 | TACATTGGGAGAAGG[ATGTGAAGAAT/C]ATGCTCAATCCCTAT | 5607 |
rs763374033 | snp | A/G | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67681493 | TCTATTTTGATGCCT[A/G]TAAAAGCCTACTGCA | 5607 |
rs763375612 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67774879 | CCTGCAGGATTGTCA[A/G]GGTTTCCCTGTAGGC | 5607 |
rs763378231 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600711 | AGACATACGATATCG[A/G]GACACTCTTGGTCAT | 5607 |
rs763380143 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552982 | TTTTTACTTGCTTTT[C/T]GGATCCCCAAAGTGG | 5607 |
rs763386231 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67620142 | TTGGGAGGTTGAGGC[A/G]GGTAGATCACCTGAG | 5607 |
rs763389282 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67729267 | AGTAATTTCTAAACA[A/T]TTCAGCTTGGCCAAT | 5607 |
rs763401435 | snp | A/C | 1.6517e-05 | 0.00287372 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67693581 | GCGGTAAGTAAACTT[A/C]TGCAAAAATAATGTT | 5607 |
rs763416592 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67720956 | CGCTTTTCAGCATTC[A/G]TGGTTAGGCTATAGC | 5607 |
rs763424325 | in-del | -/T | 0.000400805 | 0.0141507 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630869 | TCCCAAATGATTTTG[-/T]TTTTTTTTCTTCCCA | 5607 |
rs763443195 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716383 | GATGATATGCTAGGA[C/G]TAACTGAGTGGTATT | 5607 |
rs763478767 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67587345 | CTCGTAGGCCCTGTA[A/G]TGTTTGAATTTTCCT | 5607 |
rs763492832 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648749 | GCCACCATGCCCAGC[C/T]AAGTTTTGTATTTTC | 5607 |
rs763502270 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67542631 | ATGGCGCCGCGGGAG[A/G]CGGGTCCCGCTCGTC | 5607 |
rs763503982 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743352 | AGACCCACAGACATG[A/T]TAAGAACTTGAGCAA | 5607 |
rs763513818 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67646862 | CTGTGTCTTTCAGAA[A/G]GAAATCGGTTCTTAA | 5607 |
rs763514277 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67728257 | AGAGCCAGCTTTTTC[C/T]TGATACACTTTTTAA | 5607 |
rs763537687 | snp | C/T | 8.24029e-05 | 0.00641831 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67600709 | CAAGACATACGATAT[C/T]GGGACACTCTTGGTC | 5607 |
rs763541587 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552366 | GAGTACTTACTGTTG[-/T]ACAGATGCTTTGCTA | 5607 |
rs763554223 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67790374 | GTGTGAGGTCTTTCC[A/G]CAGAGCGCCCAAGGT | 5607 |
rs763557248 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67657872 | TGAAAATATTCACAT[C/T]TGCATTTCGGAAGAA | 5607 |
rs763574918 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67650421 | AGAGGGAGAGCTTTC[A/G]GTCTTTCACCATTAA | 5607 |
rs763609660 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67598919 | TGTTAGTTAATAGTA[A/C]AAATCAGGTTGTTAC | 5607 |
rs763610806 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571016 | GTATCTCCTCTGTAC[A/G]TGAGACTTGCTGCTG | 5607 |
rs763611982 | in-del | -/C | 1.65296e-05 | 0.00287481 | utr-variant-5-prime, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543307 | AGTGGGTTTCCCATA[-/C]CCCAGGATGTGAGCC | 5607 |
rs763628685 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67758438 | TTCTTGGGAGATCAC[C/T]AAGCACCTCATTCAA | 5607 |
rs763636538 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748627 | GTCTTATGTGCTTTC[A/G]CTCCTAAAGTCATTC | 5607 |
rs763639006 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67629997 | AATCCTAGCACTTTC[A/G]TAGACTGAGGTGGGA | 5607 |
rs763640552 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67603860 | GCTATGCTACATAAA[C/T]TAGATGAAGAAAATA | 5607 |
rs763641297 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67665987 | GTGGTGATAGCCATT[C/T]TAATAAGAATTAACC | 5607 |
rs763645812 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67700875 | ACCCTTAAAAGAGTT[C/T]TCTTATTTGCCATCT | 5607 |
rs763690173 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67731989 | TGTATTTAGCAGAGT[A/G]ACGGGAGATCCAGAG | 5607 |
rs763691125 | in-del | -/TG | 5.00029e-05 | 0.0049999 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772762 | TTGATGGTAAGTGAA[-/TG]TTTTTAGTTACATTA | 5607 |
rs763692849 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67652504 | ATCTTGCAGGAACTT[A/C]GAGTGAGAGTTCACT | 5607 |
rs763702519 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769593 | TGACATGTTTTTCCT[C/T]CATCACAGGATTCGC | 5607 |
rs763715922 | snp | C/G | | | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543359 | GCTAGCCCTTGGCCC[C/G]TTTCCTGCCATGGAG | 5607 |
rs763733118 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67773554 | AGTTTAGAGGTTTTC[A/G]TCCTTTGTATTCCAA | 5607 |
rs763746763 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545492 | CTTAGTTTCCTTATT[G/T]GTAAAACAGGGAAAC | 5607 |
rs763757739 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579199 | TTCCCATTAAAAAGA[A/C]TACCTGAGCAATGTT | 5607 |
rs763775637 | snp | A/C | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67543455 | CGGGCCGCAGTTACT[A/C]TTCAGGGATGTGCTG | 5607 |
rs763777043 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67584882 | TTTGTATTTTAGGTA[A/G]AGACAGCGTTTCACC | 5607 |
rs763777329 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67800717 | CACTGTATCCCCCAC[A/C]CCGATGTACGTGATG | 5607 |
rs763794418 | in-del | -/CTC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67627020 | TCACTGCAGCCTGAC[-/CTC]CTGGACTCAAGCGAC | 5607 |
rs763801807 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549468 | TGTCGAACTCCTACC[A/G]TGATGAGTGCGAGGC | 5607 |
rs763824029 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67754655 | AGGAGATGATATTTG[A/C]GCTGGGCTTTGGAAA | 5607 |
rs763833942 | snp | C/T | 3.32574e-05 | 0.00407769 | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67646431 | ATGGAGCATTTTTTG[C/T]AGAAAACAGGATTTC | 5607 |
rs763871395 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67759356 | TTGAGCTCAGGAGTT[C/T]GAGACCAGACCTGGC | 5607 |
rs763882658 | snp | C/G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67806463 | TGCTGACTACCAGTA[C/G/T]GTCACTGCTCGTCCC | 5607 |
rs763887182 | snp | C/T | 1.65132e-05 | 0.00287339 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658545 | ACATGGCATGTTTAT[C/T]TCTACAGGGGGATCT | 5607 |
rs763889747 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722650 | TTCTCTAGGACTGTG[G/T]AAATTGGTCTTGGGA | 5607 |
rs763908020 | snp | A/G | 8.35108e-05 | 0.0064613 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67769696 | CATGCCATGCCCTCA[A/G]TGTAAATGATACATG | 5607 |
rs763923601 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67779184 | CAGCAAGGGGGCCCC[A/C]CGTAGGGTCCAGCTG | 5607 |
rs763936162 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67626402 | TGTGGTGGTGGGCTC[C/T]TGTAATCCCAGCTCC | 5607 |
rs763962871 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67638450 | GTGTGTATGTACCAC[A/G]TTTTCTTTATCCAGT | 5607 |
rs763972757 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67796188 | TATACTTGAGTTTTT[C/T]GTACAGTCCTATTTT | 5607 |
rs763979034 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67677478 | GTTATTTCTTTAAAA[A/C]AAATTACCAGGATTA | 5607 |
rs763979760 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67709368 | CAAACTAGGAGGGTA[A/G]TCCTTCCCTGGAATA | 5607 |
rs763989932 | in-del | -/TATGA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67683420 | GGATTCAAGGTGGTT[-/TATGA]TATAAGGTCAATACA | 5607 |
rs764000455 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797479 | TGGATAATTTCTCCT[A/G]AGTACCTTGGAGATA | 5607 |
rs764001708 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67765594 | AAGCATTTTTCTCAT[G/T]GATGCTTTCTGTCTT | 5607 |
rs764013326 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67588013 | GGCCCATTCAGCCCC[C/T]CCTCCACCCTGCAGC | 5607 |
rs764019496 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67718662 | CAAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 5607 |
rs764027968 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67724598 | TCATGCAGCCATATC[C/T]ACTAAGAAACCATTT | 5607 |
rs764028044 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67751158 | TCATGGAACAAAGCC[A/G]GAGTTAGCTACCAGA | 5607 |
rs764041746 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67659612 | TCACTATTTTAGATG[A/G]AAATAAAAATGTTTC | 5607 |
rs764049010 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639554 | GCCGGTGACCCCCCT[C/G]CCGGCGCTGCTCACT | 5607 |
rs764081010 | snp | A/C | | | missense, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67693540 | ATTCTATAGCCAAGA[A/C]GTATGTTGGAACAAA | 5607 |
rs764081599 | snp | A/G/T | 0.000131936 | 0.00812108 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585960 | AATTGTTTCAGTAAA[A/G/T]TTAGATGGATTTGTA | 5607 |
rs764092209 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67590044 | CTGTGTATTTTTTCC[A/G]TATATGTTTCAGCTT | 5607 |
rs764124098 | snp | A/C | | | downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67807161 | GGTCTGTGACCCCCC[A/C]CAGGGCTGGGGGCAG | 5607 |
rs764135929 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748340 | TGAATGCCTTGTTTT[A/T]AACTTAGCAAATTGC | 5607 |
rs764143094 | in-del | -/AATAATAATAATAATAATAAC | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67686625 | AATAATAATAATAAT[-/AATAATAATAATAATAATAAC]ATGTTGTAGGGTTTA | 5607 |
rs764182697 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675247 | GTGGGCATTCATACC[A/G]TGGATTACTGCTCAG | 5607 |
rs764210743 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67793428 | TTTTGTTTTTGTTGT[A/G]TAGTTTTGCTAGTAG | 5607 |
rs764214260 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67767726 | TCTGTGGCCATTTTA[C/T]ATACCTTTATTGAGG | 5607 |
rs764231705 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67763788 | TTAGGGTCTGACAGG[C/T]AACACGCTATCCTGC | 5607 |
rs764265051 | snp | C/T | | | intron-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67719723 | CTGGAAATCTATCTA[C/T]TCATCTGTTGCAACA | 5607 |
rs764272314 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67745191 | CAACACACGCAAAAT[A/G]TATAAGCAGGAATGA | 5607 |
rs764280887 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67561155 | GAACTTCATAAAGAA[A/C]AAATCAGTTTAGCCT | 5607 |
rs764300951 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67792137 | GTTTGCAAAAGGAGG[-/T]TAAGATCAAAGGAAC | 5607 |
rs764310471 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67740455 | ACAACTTGTCTTCAC[A/G]TGGGCACACACCTGT | 5607 |
rs764315758 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67589141 | GAACCACCACAGCTG[G/T]CCTTTAAATGTTTTT | 5607 |
rs764330803 | snp | C/G | 1.77153e-05 | 0.00297612 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642464 | ACATATTGAGGGCCA[C/G]AGCTAGAGATGAATT | 5607 |
rs764332314 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67682862 | AAAGAGTTGTAGGCT[A/G]GGTGCAGTGGCTCAT | 5607 |
rs764350942 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67730075 | GATGCCGTTAGGCCT[A/G]TTTCCTAAGTTTTTC | 5607 |
rs764352502 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67648080 | TATTGAAATATAACT[C/G]AGATACCATAAAATT | 5607 |
rs764373922 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67549948 | TCAAAAATCTTTCCC[A/G]GGTTCTCATATTTCC | 5607 |
rs764376310 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67596470 | GAAAAAAAAGGGAGG[A/G]GGAATATATATCTAC | 5607 |
rs764397457 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67775352 | GTATTTTAAAGTTGG[A/G]CCAAGAAATTCCTTT | 5607 |
rs764406968 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67666101 | CATTCTTAATAGTAA[A/G]GCTTTCTTTAAAAGG | 5607 |
rs764408890 | snp | C/G | 4.94238e-05 | 0.00497086 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67550054 | GATAGGCCAGGTTCT[C/G]CCTGAAGCAACAACT | 5607 |
rs764413862 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67762370 | ATGGCTGATGACCAA[C/T]AAGAGACCTAAAATA | 5607 |
rs764430726 | snp | C/T | 0.000101245 | 0.00711424 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67630870 | CCCAAATGATTTTGT[C/T]TTTTTTTCTTCCCAT | 5607 |
rs764439300 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67609340 | ACACTAGTGGGGCAA[A/G]CAATAATCAAGACAA | 5607 |
rs764440289 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67635426 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 5607 |
rs764456643 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67738250 | TTTGTTTTCTGTTCA[A/G]AAACAAGTTGCAGAG | 5607 |
rs764463826 | in-del | -/AA | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67716837 | AATGTAACACTTAAC[-/AA]AGCTATTTGGTATTC | 5607 |
rs764467099 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67805219 | CCTCTGAGATAGACC[C/T]ACGCAGGGTGTCCCC | 5607 |
rs764468622 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67727905 | TAGACAAATATTATT[C/T]CCTTTCCCAGCTTGC | 5607 |
rs764473354 | snp | A/G | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548763 | AAATAATTTTTTAAC[A/G]CTAAAATCTTTTATA | 5607 |
rs764502448 | snp | A/G | 5.09256e-05 | 0.00504581 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67772801 | CAGTTATATATTTAT[A/G]TTTAACATTCTGTTT | 5607 |
rs764515449 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655593 | CTCTTGTTCTTTTGA[A/G]GATTATTTGTAATTG | 5607 |
rs764542943 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606523 | AGGAGGGAAGGAATT[G/T]TCATTCTCAAAGATG | 5607 |
rs764578708 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67781587 | GACATTTGCTGGAGT[A/G]TGGACTAGTTTCTTT | 5607 |
rs764582641 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67794108 | TTATTTGTAACCAAA[A/G]TGTGCTCCCTCAGTC | 5607 |
rs764587666 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67628979 | CAATTTCAACAATCA[G/T]TCTTCAAATTTCAGA | 5607 |
rs764607520 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67595155 | GGGACATGATTCTTC[A/C]AGATAATCAAATATT | 5607 |
rs764613854 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799898 | CAGGGGAGGGCTGAC[C/T]GACTCTTAGCCAGGG | 5607 |
rs764634842 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67623180 | ATTTTCCTGTTAACC[C/T]AAGGAGAATGAAAAC | 5607 |
rs764643102 | snp | A/C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67752214 | GGGACTACAGGCACA[A/C/T]GCCACCACACCTGGC | 5607 |
rs764682840 | snp | G/T | 3.53907e-05 | 0.00420644 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67642475 | GCCAGAGCTAGAGAT[G/T]AATTTTGATGGAGGA | 5607 |
rs764685982 | snp | G/T | 1.64863e-05 | 0.00287104 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67550009 | AAGATGGCTAATTGT[G/T]TTTCTTTATTCTTTC | 5607 |
rs764686463 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67732363 | GATGATAGCAAATCC[A/G]TTAAGGAGACTTCTC | 5607 |
rs764725237 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67702945 | GATAATATCATATAA[G/T]GTTGTGTAATTTGTT | 5607 |
rs764728916 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67651938 | TTTTGAGGAATTTCC[A/G]TACTGTTTTCCATGG | 5607 |
rs764736025 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67735783 | CCAGAAATAGAATAG[A/T]AGGTTAAAGTAATGA | 5607 |
rs764740482 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562181 | TGCTCCAGACGTTTT[C/T]GGCATTTCTTTCAAC | 5607 |
rs764769755 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67618794 | CATCACTGTTTTCTT[G/T]CTACCCTATTCAAAA | 5607 |
rs764777830 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67748818 | CTATCCCGCAGGCTG[C/G]TCCTCAGGGGCATCA | 5607 |
rs764779502 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67606604 | GCAGTGGGCTGGGGA[C/T]GGTCCTTGGAGGTGG | 5607 |
rs764783302 | snp | G/T | 3.29875e-05 | 0.00406112 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67543484 | TGGTGAGTGGTAATC[G/T]CAGTGTCCGGATGCC | 5607 |
rs764806105 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67655556 | CCCTGCCTCTGACCT[C/T]TGGTTTCTGATGAGT | 5607 |
rs764808942 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67545209 | CCCCACCTCTGTGTC[A/G]TCACAGCTTTGTGTG | 5607 |
rs764821202 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67675483 | ATGGAGCAAGATGAG[A/G]AATCCTCATGGTGAT | 5607 |
rs764837402 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67558918 | CAGTGCCCACCACAT[A/C]GTGGGTACTTTTATT | 5607 |
rs764839917 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67639763 | GTGTGTCTTTTAAGT[G/T]GAACTCGTTGCCTTA | 5607 |
rs764848334 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67760900 | CAGTTACCCAGCAGC[C/T]TGGGCTGGGGGCACT | 5607 |
rs764851104 | in-del | -/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67679876 | TACTCAATTCAGTGA[-/T]TTTTAGTAAGTTTAT | 5607 |
rs764858522 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67571087 | TCTATATCAGTTCCT[C/T]TCTGGATTCTTCCTG | 5607 |
rs764859617 | snp | A/G | 1.65012e-05 | 0.00287234 | synonymous-codon, nc-transcript-variant | MAP2K5 | GRCh38.p7 | 15:67658569 | GGGATCTTTGGATGT[A/G]TATAGGAAAATGCCA | 5607 |
rs764861286 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP2K5, LOC107984718 | GRCh38.p7 | 15:67722785 | ATGAAGATTTAACTG[C/T]AGCGCACAATCTAAA | 5607 |
rs764864262 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67552161 | TCAACAATCATTGCC[C/T]GTTTTTAAAAGCTAT | 5607 |
rs764884167 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67599127 | AAAATTTATCATTCG[A/G]TCCAGAATAATGAGA | 5607 |
rs764900730 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67566195 | TTGTTTTGTTTTTGA[A/G]ATGAAGTCTCATTCT | 5607 |
rs764915171 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660755 | TGCAAGATGAGGTTT[A/G]GAAAAGTTAACCAGC | 5607 |
rs764925167 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696036 | GTAAGGTTGGGGGTG[A/G]GGGGAGGTGGAAATA | 5607 |
rs764951372 | in-del | -/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67660283 | CCTCCAAAATGTAGT[-/T]GTTTTTTTTGTATGT | 5607 |
rs764967002 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67743732 | AGTTTTAATATCCAG[C/G]ACAGTGCCAGATAAA | 5607 |
rs764979740 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67799126 | GTGAGCCGAGATCGC[A/G]CCACTGCCCTCCAGC | 5607 |
rs764988559 | snp | G/T | 1.6517e-05 | 0.00287372 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67585981 | TGGATTTGTAATGCT[G/T]TGTTCCACTTATTGA | 5607 |
rs765000350 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777595 | TCTGTATGTAAATGC[A/G]TGAGGCACAGCTGGA | 5607 |
rs765008065 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67749725 | CCTGAAACAAATGGA[A/G]GCTCCATTATCTCAA | 5607 |
rs765017797 | snp | G/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67797629 | GGTATAGATTTTATA[G/T]TTATTTTACTTGGAA | 5607 |
rs765040281 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67676133 | CCCCAGTGTGTGGAT[A/G]AGTGTTTGATTCACC | 5607 |
rs765053920 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67569080 | TTTTGTCCTTACCTA[C/T]AAGGCTGTGTTTTAC | 5607 |
rs765054774 | snp | A/G | 0.000130625 | 0.00808056 | intron-variant | MAP2K5 | GRCh38.p7 | 15:67658802 | TCACAACATAGTCAC[A/G]CGCTTATGTGCTCCA | 5607 |
rs765068086 | in-del | -/TGT | 6.51232e-05 | 0.00570591 | utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67806775 | GGGCACTGAAAGCCC[-/TGT]AGGACCAGTAACCAA | 5607 |
rs765074760 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67768293 | TGTGCAATTGTATCT[A/G]TCTGCCACCATTGAT | 5607 |
rs765111532 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67785475 | GTAGGGAATACAGAG[A/G]GCTATCAGACACTAA | 5607 |
rs765136097 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67581097 | CTTTTGGGGGTCCAC[A/G]TGGTTTCTAAAGCAA | 5607 |
rs765142721 | snp | C/T | | | intron-variant, utr-variant-3-prime | MAP2K5 | GRCh38.p7 | 15:67662162 | AATCTTTCAGGAGCA[C/T]ATTGCACCCTTTGAG | 5607 |
rs765176576 | snp | A/C | | | upstream-variant-2KB | MAP2K5 | GRCh38.p7 | 15:67542101 | TTTAGGGCACTCGTG[A/C]GGTAAAGAACTTCAC | 5607 |
rs765193125 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67613448 | TGTGAAAGACCAGCT[A/G]TTTGGGATATATCTA | 5607 |
rs765207646 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67673539 | GAAAGAAATTTTGAT[A/G]TCAAGGTGGTAGTTA | 5607 |
rs765208111 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67579277 | TGTGTGCCGAGGACA[A/G]GTCATTTTCGGACAA | 5607 |
rs765211901 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67696855 | GTGGTGGTGCATGCC[A/T]GTAATCCCAGCTACT | 5607 |
rs765220186 | snp | C/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67706357 | CTCATTGAATTTTCA[C/G]GATCGAAGAGGATTA | 5607 |
rs765240365 | snp | C/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67691859 | GAAGGATAAATGAAA[C/T]AAAGACTAATAAGCA | 5607 |
rs765251220 | in-del | -/A | | | upstream-variant-2KB, intron-variant | MAP2K5 | GRCh38.p7 | 15:67548913 | ACAGATTTATTTTTG[-/A]AAAAAAAAAAAAAGC | 5607 |
rs765283177 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67783364 | TGTGGAGTCCTGTGC[A/T]CCAAACTTCTGGCAG | 5607 |
rs765312963 | snp | A/T | 1.65228e-05 | 0.00287422 | intron-variant, downstream-variant-500B | MAP2K5 | GRCh38.p7 | 15:67703424 | GTACGTTGTTTGCAC[A/T]TAGACGCTTCTGTGC | 5607 |
rs765320852 | snp | A/T | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67562470 | CATGAAATAAATACA[A/T]TATTTCTAGATGTGG | 5607 |
rs765359817 | snp | A/C | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67753232 | ATGTAAGAGTAAAAA[A/C]TACAAAATTCTCAAA | 5607 |
rs765367245 | snp | A/G | | | intron-variant | MAP2K5 | GRCh38.p7 | 15:67777746 | TAGTAATTGTTTAAA[A/G]ACATGGGTTTTCTCC | 5607 |