SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12959 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597814 | AGCCAGGGTTGGAGT[C/T]TTAGCCTCGGGATCC | 4296 |
rs948577 | snp | A/G | 0.270621 | 0.249148 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597847 | GCCAGGGCTCTCTGG[A/G]TGCCTTCCTGCTGCC | 4296 |
rs1051652 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597867 | TGCCCTGGGGGTCAT[C/T]TGGGGCCAGGGCTCT | 4296 |
rs1078457 | snp | A/G | 0.264084 | 0.249603 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612653 | TAAATTCATGTTCGT[A/G]GAGTTGGTGCTCTGT | 4296 |
rs1078458 | snp | A/G | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612623 | TCCTCCCCTCCCGTC[A/G]TCATGGGCAGCTCCT | 4296 |
rs1144787 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609943 | GGACGGTGGGGCAGC[A/G]GGGACAGCTGGCAGC | 4296 |
rs1151488 | snp | A/G | 0.323671 | 0.238899 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604133 | TCATGAATAGTTCAG[A/G]TCAGTGACAAACTTC | 4296 |
rs1151527 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606150 | ACAGTCAGGCTTCAG[A/G]GATAAACTTTAGAGT | 4296 |
rs1194080 | snp | C/T | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602379 | ggccgggcatggtgg[C/T]tcacgcctgtaatcc | 4296 |
rs1211565 | snp | C/T | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602386 | catggtggttcacgc[C/T]tgtaatcccagcact | 4296 |
rs1318715 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604496 | cacagagGCAGAGCC[C/G/T]TGGCCTCCATCTGCC | 4296 |
rs1383042 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604495 | acagagGCAGAGCCC[G/T]GGCCTCCATCTGCCC | 4296 |
rs1679085 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606453 | TCTAAATGCTTTGCT[A/C]ATATTAATTTCTTGC | 4296 |
rs1784223 | snp | C/T | 0.385168 | 0.210309 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612777 | ACCAATTTCTTAACT[C/T]GTCCAAACCGCAGCT | 4296 |
rs1787034 | snp | A/G | 0.36315 | 0.222928 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615093 | AAGAGAGCCTTAGGC[A/G]ATCCACTCCAAGAGC | 4296 |
rs1787035 | snp | A/G | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614677 | AGAAGAAAAAAGAAA[A/G]AAAATAATGAGGCTC | 4296 |
rs2004649 | snp | A/G | 0.489124 | 0.0729368 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613445 | CTCGCAGGGGCGGCC[A/G]CCACCCCGAGACACA | 4296 |
rs2230486 | snp | A/C/G | 0.101108 | 0.205668 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613682 | CAGCGGGGGTGGTGG[A/C/G]GGCGGTGGAGGAGGC | 4296 |
rs2306360 | snp | A/T | 0.0887219 | 0.191022 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607067 | GCATGTCGGTCTGGG[A/T]GTGGGAAGGGGTGGG | 4296 |
rs2306361 | snp | G/T | 0.496583 | 0.0411924 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607024 | TCTGGGAAGGTCTAG[G/T]GGGCGGGGCCGGCCG | 4296 |
rs2509950 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602802 | agaacaagactcctt[C/T]ttaaaaaaaaaaaag | 4296 |
rs2510079 | snp | G/T | 0.0198 | 0.0975088 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609013 | agcagggaaatgact[G/T]ggcagaggtcataca | 4296 |
rs3016416 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608710 | gcaacctccacctcc[G/T]gggttcaagcgattg | 4296 |
rs3016417 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608724 | ctgggttcaagcgat[G/T]gtcctgccccagcct | 4296 |
rs3016418 | snp | G/T | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608749 | cagcctcccgagtag[G/T]gggattatgggcatg | 4296 |
rs3017079 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608820 | gagacccgcctgacc[A/C]acatggagaaaccct | 4296 |
rs3017080 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608686 | aggttgccgtgagcc[A/C]agatcacgcccttgc | 4296 |
rs3814751 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615305 | CCTTCCGTAACAGGC[A/G]GGAATAGTCGAAATA | 4296 |
rs3825069 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613844 | CGGATGCCCAGGTTC[C/T]GGGACTAGGGCCTTG | 4296 |
rs3825070 | snp | A/G | 0.170408 | 0.236992 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612403 | TCCCCAACCCACAGC[A/G]GGTCCTCAGCCATGG | 4296 |
rs4326800 | snp | C/T | 0.363803 | 0.222596 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599782 | ACCTGCGGGCAGAGG[C/T]GGCACAGGTGAGGGT | 4296 |
rs4608078 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600108 | GGGGCAACCTCCAGG[C/T]CCAGGGGCATGGCAG | 4296 |
rs7116712 | snp | C/T | 0.460365 | 0.13508 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605047 | CTCACTACGAGAGCA[C/T]TGGAGCTGAAGCCTC | 4296 |
rs7122657 | snp | C/T | 0.310878 | 0.242475 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610557 | TGAGCATTTAGCAAG[C/T]CCCCGACGACAAGCT | 4296 |
rs7130955 | snp | C/T | 0.475613 | 0.107697 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605109 | GGTAGGTTACTTCAC[C/T]TCTCAGAGCCTCAGT | 4296 |
rs7481611 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614660 | TGCGATCCATCGATT[C/T]TGAGCCTCATTAttt | 4296 |
rs7924612 | snp | A/G | 0.00042287 | 0.0145347 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605741 | CAGCCAGATCCTGCC[A/G]GGGGAGGAAGGCCAC | 4296 |
rs7929981 | snp | A/T | 0.0275645 | 0.114116 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615705 | CGTCCTACCGCGCCA[A/T]CACCTTTCTGCGCTT | 4296 |
rs7932616 | snp | C/T | 0.270621 | 0.249148 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598769 | GCCCTTCCTGCTCCG[C/T]GGTGCCTCTGTTTTT | 4296 |
rs7934992 | snp | C/T | 0.163236 | 0.234461 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604444 | CTGCAGGACAGATGC[C/T]GGGGGCAGTGCAGCT | 4296 |
rs7946115 | snp | C/G | 0.270621 | 0.249148 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598721 | CCTCAGTTTCCCCAT[C/G]TGCACAGTGACCTAC | 4296 |
rs10444358 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614528 | GTTGGTCTCTGCTAA[A/G]GATGGGCCATCTCTG | 4296 |
rs10526208 | in-del | -/CTTTTTT/TTTTCTTTTTT | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614687 | TTTCTTTCTTTTTTC[-/CTTTTTT/TTTTCTTTTTT]CTTCTTTTGAGACGG | 4296 |
rs10750762 | snp | A/G | 0.271162 | 0.249103 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600834 | CTGGAGTGCAGCAGC[A/G]GGTTGGATGTCGGGA | 4296 |
rs10750763 | snp | A/G | 0.271702 | 0.249056 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600963 | CCTCTTACCTCACCC[A/G]ACTCCCACCCCGGCC | 4296 |
rs10791820 | snp | C/T | 0.369288 | 0.219705 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599376 | ATATGTGAAGCAGGC[C/T]GGCTTCAGGCCACTC | 4296 |
rs10791821 | snp | A/G | 0.233818 | 0.249476 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600852 | TTGGATGTCGGGAGG[A/G]AGAAATACAAGGCTG | 4296 |
rs10896020 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597306 | GGCCTATGGTTTTTT[G/T]TTTTTTTTTTTTTTG | 4296 |
rs10896021 | snp | C/T | 0.270621 | 0.249148 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597440 | CCAGAGTAGCTGGGA[C/T]TACAGGCATGCACCA | 4296 |
rs10896022 | snp | A/C | 0.270621 | 0.249148 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599139 | TGCTGGGATCACAGG[A/C]GTGCACCACTGCCTG | 4296 |
rs11227234 | snp | G/T | 0.270621 | 0.249148 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597700 | GCATCAGGACACCAG[G/T]GTTGTATGATAGGTT | 4296 |
rs11227235 | snp | A/T | 0.270621 | 0.249148 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599024 | GAGTTTGCTACGATT[A/T]TGATTACATGTATGC | 4296 |
rs11227236 | snp | C/T | 0.000187108 | 0.00967053 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599514 | TGAGCGAGAAGCAGA[C/T]GAGCGGGGAAGGGGG | 4296 |
rs11227237 | snp | C/T | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599614 | TGGGCCTCCCGGCGG[C/T]TGCAGGTCGCGGCCA | 4296 |
rs11227238 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606347 | GATTCTGGCTCTTCC[A/G]CTTATTAACTGTGTA | 4296 |
rs11227239 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612533 | tgaagccagggaggg[C/T]taggccagaattcca | 4296 |
rs11227240 | snp | C/G | 0.0475351 | 0.146656 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612914 | GGGACCCCCTAGGGT[C/G]GGAGCTCCTACCTGC | 4296 |
rs11282819 | in-del | -/GTCTTG | 0 | 0 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597516 | CATGTGGCCAGGTTG[-/GTCTTG]AACTCCTGACCTCAT | 4296 |
rs11378063 | in-del | -/T | 0.0633504 | 0.166319 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601831 | ACCACGAGGTTATCA[-/T]TATCACCCCCACTTC | 4296 |
rs11541016 | snp | C/T | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598535 | GCCTCATCAGCCGAC[C/T]TCGGCCCTCGCCCCT | 4296 |
rs11824024 | snp | C/G | 0.0147138 | 0.084501 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606674 | CGGAGAGGGGCATGA[C/G]AGGTGAAGTTTCTTA | 4296 |
rs12419237 | snp | C/T | 0.406468 | 0.194981 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597606 | TGGCCGAGAAGAGCC[C/T]TGAATGACTGACCAA | 4296 |
rs17855262 | snp | A/G | 0.00732812 | 0.0600863 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613535 | TCCTGAGATGGCTGC[A/G]TCCCGGGACAGCACC | 4296 |
rs17855912 | snp | G/T | 0.00556005 | 0.052432 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608433 | TCGTCACTCTCAATG[G/T]GCTGCAGCAGCAAAA | 4296 |
rs34178129 | snp | A/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613305 | ACACTGATGTCCTCA[A/T]CGGGGTCCTGGCGAG | 4296 |
rs34491061 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598765 | ACCGCCCTTCCTGCT[-/A]CCGTGGTGCCTCTGT | 4296 |
rs34555075 | in-del | -/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603629 | TCTTAGCTGGGTTTC[-/G]GGGGGGTGGCTGTGA | 4296 |
rs34559454 | in-del | -/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611806 | GTGCCTTCGGGGAAT[-/C]CCCCCTCAGATTGGG | 4296 |
rs34594252 | snp | C/G | 9.89495e-05 | 0.00703313 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608343 | GCGTAGGTGCCCGCG[C/G]CACTCATTTGTGTGG | 4296 |
rs34634549 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616280 | CCATGAGGGTCCCGG[-/T]GAGGGGGGGCGCGGG | 4296 |
rs34686164 | in-del | -/A | 0.429238 | 0.174281 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601769 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGC | 4296 |
rs34837604 | in-del | -/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607865 | AAGGGGTCCGTGGGT[-/G]GGATGTGTCCTGGGC | 4296 |
rs34876918 | in-del | -/A | 0.349233 | 0.229462 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602203 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 4296 |
rs35274097 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613568 | CACACGGTCACCCTT[-/C]CTCAGGGCCAGCTCA | 4296 |
rs35487354 | snp | C/T | 0.0220325 | 0.10262 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599411 | CGGGGCTCCTCCTCA[C/T]GTCGGGGGCTCTTGG | 4296 |
rs35570382 | in-del | -/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611215 | GTCTCCCACTTGGGA[-/G]GGGGGAGTCCTTTTG | 4296 |
rs35596116 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599306 | TGGTCTCGGCCTTGC[-/A]CTCCTTGCATGTCCC | 4296 |
rs55649236 | snp | A/T | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607929 | CCTCTTACCGGCCAT[A/T]AGCTGTGCGAAGGGC | 4296 |
rs56076163 | snp | C/T | 0.350764 | 0.228794 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600819 | CCTTTCCCCTCCTGC[C/T]TGGAGTGCAGCAGCA | 4296 |
rs56369260 | snp | C/T | 1.7251e-05 | 0.00293687 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613655 | CGCTGCCTTTGGAGA[C/T]CCCTCAGGCCGGCCT | 4296 |
rs56397033 | snp | A/C | 0.0614824 | 0.164198 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610892 | GCTGCTAAGCCCCAT[A/C]CTCTGCTTTCTCTCC | 4296 |
rs56961224 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611749 | TCCATTTTTTCTGGA[A/G]AGAAAACGGAGGAAA | 4296 |
rs58593829 | snp | A/G | 0.284995 | 0.247539 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599970 | GGAGGGGAGGGCAGT[A/G]CAGGTGGAGGAAGCG | 4296 |
rs58661068 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611681 | CGGCTCAGGGGCAGC[A/C]GGAAACGCAGGAAGC | 4296 |
rs58950470 | snp | C/G/T | 0.501258 | 0.0412654 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616284 | TGAGGGTCCCGGGAG[C/G/T]GGGGGCGCGGGCAGC | 4296 |
rs60166956 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601743 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 4296 |
rs60500255 | in-del | -/CC | | | frameshift-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598369 | TCCTGGGGGCCCCCC[-/CC]TGGAAGGGGTTGGCA | 4296 |
rs61113739 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602221 | AAAAAAAAAAAAAAA[-/A]GCAAGAGAGGCTGGG | 4296 |
rs61736581 | snp | A/G | 0.000164978 | 0.00908086 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608330 | AGGAGCCATCCAGGC[A/G]TAGGTGCCCGCGGCA | 4296 |
rs61736582 | snp | A/G | 0.00269874 | 0.0366345 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606067 | CCCATGCCTGGCCTG[A/G]CTCTGCAGGCTCCAC | 4296 |
rs61893790 | snp | A/C | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602204 | TGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 4296 |
rs61893791 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608181 | TTGGGTCCCTGTCCC[A/T]GGACTTGGCCCAGCC | 4296 |
rs61893792 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608851 | GAACTCCCAACCTCA[G/T]GTGATCTGCCCGCCT | 4296 |
rs61893793 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608858 | CAACCTCAGGTGATC[C/T]GCCCGCCTCGGCCTC | 4296 |
rs61893794 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608862 | CTCAGGTGATCTGCC[C/G]GCCTCGGCCTCCCAA | 4296 |
rs61893795 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608879 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 4296 |
rs61893796 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608885 | CCTCCCAAAGTGCTG[G/T]GATTACAGGCCACTG | 4296 |
rs61893797 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608889 | CCAAAGTGCTGGGAT[G/T]ACAGGCCACTGCACC | 4296 |
rs67320473 | in-del | -/TTGGTC | | | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597514 | ACCATGTGGCCAGGT[-/TTGGTC]TGAACTCCTGACCTC | 4296 |
rs71893595 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614678 | TCATTATTTTCTTTC[-/T]TTTTTTCTTCTTTTG | 4296 |
rs76029898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604756 | GGAGTGAGTTTAAAC[A/G]GCTTGCTGAACAGGA | 4296 |
rs76099540 | snp | A/G | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602220 | AAAAAAAAAAAAAAA[A/G]AGCAAGAGAGGCTGG | 4296 |
rs76347929 | snp | A/G | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603450 | GTTGCTATCAGCGTA[A/G]CTGAGTGCACCCTGC | 4296 |
rs76733203 | snp | C/T | 0.00237929 | 0.0344091 | synonymous-codon, upstream-variant-2KB | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616336 | CAGGTGTTGCAGATC[C/T]TGCGCCAGGGGGTGT | 4296 |
rs76854022 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609693 | ATGTTTCTGGACCCA[C/T]GTCAGGGCACACCTC | 4296 |
rs76984126 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609766 | CATAGGGCACAGGGG[G/T]TGGGGCAGATGGGAA | 4296 |
rs77283952 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612478 | CTTTTTACAGATTCT[A/G]AAATTGAGGCTCCGA | 4296 |
rs77796611 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609487 | CCCAAATGGGGCCAC[C/T]GTACTTGGTACAAAG | 4296 |
rs77894452 | snp | C/T | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608631 | TTCCTTTTTTTTTTT[C/T]CTTAAGATAGAGTTT | 4296 |
rs78369580 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610793 | GGAATCTGAGGCCCA[C/G]AGAGGGGCAACAACT | 4296 |
rs78416147 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604180 | GTAGTTTCTCTTCAT[A/G]AATAATTAACAAATT | 4296 |
rs78509632 | snp | A/C | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603494 | CTTGCAGCCAGCTCT[A/C]CAGGGACCAGAACAG | 4296 |
rs78833410 | snp | G/T | 0.0137898 | 0.0818824 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613775 | CGGGAGCCGGCGCTG[G/T]GATGTGTGGAGGACC | 4296 |
rs80068959 | snp | A/T | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606514 | TTTGACTAAAAAAAA[A/T]TAAGTAAAATTAATG | 4296 |
rs80274643 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615038 | CTAGTTGGATGGGGT[A/G]GGGAAGACTGGAGGA | 4296 |
rs111242671 | in-del | -/TTGGTC | 0.0463947 | 0.145069 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597513 | CACCATGTGGCCAGG[-/TTGGTC]TTGAACTCCTGACCT | 4296 |
rs111335742 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601360 | CACAGTTATTGCTCA[C/T]GTTATGCCTCATAGA | 4296 |
rs111340550 | snp | C/G | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597622 | TGAATGACTGACCAA[C/G]GCTGGTGGATTTGGT | 4296 |
rs111379327 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613995 | GGTGGGGCCCCGGGG[A/C]CTCCGGCGCCTCACC | 4296 |
rs111453165 | in-del | -/C | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610557 | TGAGCATTTAGCAAG[-/C]CCCCGACGACAAGCT | 4296 |
rs111959656 | snp | A/C | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597395 | GCAACCTCCACCTTC[A/C]AGGTTCAAGCAATTC | 4296 |
rs112101273 | in-del | -/T | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608631 | TTTCTTTTCTTTTCC[-/T]TTTTTTTTTTTCTTA | 4296 |
rs112392106 | snp | G/T | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604601 | CTCAGTTTTCTCTGT[G/T]GTAAAATGCAGGCCA | 4296 |
rs112593823 | snp | A/G | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609803 | CTAATACAGCCTGGT[A/G]AGTCAGGGAAGACTT | 4296 |
rs112629622 | in-del | -/A | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606505 | TACAATTATTTGACT[-/A]AAAAAAAAATAAGTA | 4296 |
rs112753386 | snp | A/T | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601613 | CACAAAAAATTAGCC[A/T]GGCGTGGTGGTGGGC | 4296 |
rs112995557 | snp | A/G | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608590 | AGATCTTGAGGACCT[A/G]CTTGAGGTCAGACAT | 4296 |
rs113014372 | snp | A/G | 4.01727e-05 | 0.0044816 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599540 | GGGGGCGGCTCGGTC[A/G]GGCAGGGCGCGGGCG | 4296 |
rs113245537 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614958 | GGGATTACAGGCGTG[A/G]GCCACCGCGCCCGGC | 4296 |
rs113324277 | snp | C/G | 0.5 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606929 | GATGGCTGTGAGACT[C/G]TGACCAGCCTCACTG | 4296 |
rs113489940 | snp | A/C/T | 0.00380691 | 0.0434675 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599575 | CGTGGGGGGTGTTGT[A/C/T]GGGGACTCCCCGCGC | 4296 |
rs114123593 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612726 | TTGAGGTGGGAGCCA[C/T]GGCTGGGCAGGATGC | 4296 |
rs114178937 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605546 | CTCTGGGCCCCGAGC[C/T]GAGGCCTGGGCTGTA | 4296 |
rs114635642 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609142 | AGCTCTGGACATTTA[C/T]GGCTTTGATTTCAAG | 4296 |
rs115625190 | snp | C/G | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614112 | GGCCTTCAGGGGCAG[C/G]GCCTCAACTCCGGTT | 4296 |
rs116621217 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604196 | AATAATTAACAAATT[C/T]TTTGGATAAAAAAAC | 4296 |
rs116904048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608933 | ACATTTCACACTCAA[C/T]CCCAGCACTCAAAAC | 4296 |
rs117090535 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605044 | GAGCTCACTACGAGA[C/G]CATTGGAGCTGAAGC | 4296 |
rs117309574 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599885 | TCTACTAGCATCTTC[C/T]CTGGTCCCACAGGTC | 4296 |
rs117393001 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603051 | GAGTTTGCAGTGAGC[C/T]ATGATCATGCCATTG | 4296 |
rs117592462 | snp | C/T | 0.029116 | 0.117091 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601484 | TCCCTGGGCCAGGCG[C/T]GGTGGCTCACATCTG | 4296 |
rs117897057 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604652 | GAACTGCTTGGCACA[C/T]AGAAGAGAACCAACA | 4296 |
rs137905129 | snp | A/G | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599698 | CTTGGGCGTCCCAGA[A/G]CTGCTACCGCGCTCT | 4296 |
rs138202182 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614876 | GGAGACGGGTTTCAC[C/T]ATGTTGGCCATGCTG | 4296 |
rs138241338 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610630 | GTGGAAATGGGCACC[C/T]CCCCTGGTGCCAGGG | 4296 |
rs138254027 | snp | C/T | 0.000303669 | 0.0123184 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613539 | GAGATGGCTGCGTCC[C/T]GGGACAGCACCTCCA | 4296 |
rs138287989 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602713 | CTGGGGAGGCTGAGG[A/G]AGAATTGCTTGAACG | 4296 |
rs138504384 | in-del | -/TC | 0.0115144 | 0.0749975 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612062 | CCCCCTCTAAGAATG[-/TC]CTCATGCTTTTCCAG | 4296 |
rs138509783 | snp | C/T | 7.82396e-05 | 0.00625409 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599530 | GAGCGGGGAAGGGGG[C/T]GGCTCGGTCGGGCAG | 4296 |
rs138950634 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609390 | TGGGGTCCAAGAAAG[C/T]GATGGTTCTTGGCCA | 4296 |
rs138968470 | snp | A/C/G | 0.00010017 | 0.00707648 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605781 | AGTGCTGGGGGTGTG[A/C/G]AAGGAGATCCTAAGG | 4296 |
rs139047246 | snp | A/C/T | 3.38331e-05 | 0.00411286 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613633 | TCCACACCGGGTTGG[A/C/T]ATAACCCGCTGCCTT | 4296 |
rs139170020 | snp | A/G | 4.96225e-05 | 0.00498084 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608295 | CTGCCCTTAGAGAAG[A/G]TGGAGGCCTTGATAA | 4296 |
rs139631977 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603828 | ATACTTATCAAGAAC[A/G]GTAACTACCATGGTT | 4296 |
rs140078540 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614688 | TTTTCTTTCTTTTTT[C/T]TTCTTTTGAGACGGA | 4296 |
rs140210985 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613346 | AGCCACCAGCTCACC[C/T]CGCCAGCTGCCCCTG | 4296 |
rs140542060 | snp | C/G | 0.0314385 | 0.121371 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615947 | CTAGGGAGCTGTCGC[C/G]TGCACCCCGGGAGCA | 4296 |
rs140564989 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613478 | GTTGGACGGGAAGAT[A/G]CCCACCTGGCCACCC | 4296 |
rs140685074 | snp | C/T | 5.032e-05 | 0.00501572 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607788 | GGAGGCGAAGTCGGG[C/T]CTGCGGTGGGGGTCC | 4296 |
rs140704417 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614773 | ACCTCCGCCTCCCGG[A/G]TTCAAGAGATTCTCC | 4296 |
rs140744853 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601166 | CTCTCAACTCTTCTC[A/G]GAGTTCAGCCAGGTT | 4296 |
rs140749201 | snp | C/T | 0.000188583 | 0.00970855 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599518 | CGAGAAGCAGATGAG[C/T]GGGGAAGGGGGCGGC | 4296 |
rs141071251 | snp | A/G/T | 5.00516e-05 | 0.00500237 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607954 | AAGGGCTCGGGGCAG[A/G/T]TGGATGGGATGGGCA | 4296 |
rs141168736 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612824 | GACTTCTGAAGCTGG[C/T]GCAGGAAGACTCTGC | 4296 |
rs141208028 | snp | A/G | 0.000366233 | 0.0135271 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605885 | AGGAGGGGTGCTTTA[A/G]GAATTTCAGGACTTG | 4296 |
rs141395683 | in-del | -/TTTCTTTTTTT | 0.0182019 | 0.0936463 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614677 | AGCCTCATTATTTTC[-/TTTCTTTTTTT]CTTTCTTTTTTCTTC | 4296 |
rs141657750 | snp | C/G | 0.00010058 | 0.00709083 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605773 | CACCATTGAGTGCTG[C/G]GGGTGTGGAAGGAGA | 4296 |
rs141918760 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609606 | ATAGAGTCATGAAGG[C/G]TCTGAAGGGCCCCTC | 4296 |
rs142183438 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609592 | AGAGGACAAAGTCAT[-/A]AGAGTCATGAAGGGT | 4296 |
rs142270844 | in-del | -/C | 0.19459 | 0.243782 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615839 | CTCCTTAGGCCGGCA[-/C]CAGCAGAAGCCGGGC | 4296 |
rs142617713 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611595 | CCGCAAGTCCTCCAC[C/T]CCAAGCTCTTTCCTC | 4296 |
rs142837728 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610664 | ACCTTCCCCTTTGAA[A/G]ACCAACACTTGCTGC | 4296 |
rs142992228 | snp | A/G | 1.69925e-05 | 0.00291478 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613641 | GGGTTGGCATAACCC[A/G]CTGCCTTTGGAGACC | 4296 |
rs143344696 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604276 | TCTGGGAGCTGAGGG[A/C]CAGAGAGTTCTGTGG | 4296 |
rs143383615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599019 | GCCAGGAGTTTGCTA[C/T]GATTATGATTACATG | 4296 |
rs143451767 | snp | C/G/T | 7.2264e-05 | 0.00601062 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613131 | ACATGGGGAGGCACG[C/G/T]GCCGCCCGGCCAGAG | 4296 |
rs143609435 | snp | A/C/G | 7.22093e-05 | 0.00600836 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599451 | GGCCCACAGGGATAC[A/C/G]CAGGTCCAGCAACAG | 4296 |
rs143616577 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600493 | GTGAAAGGTGGAGCC[A/G]GCCTCACCCCAGGCA | 4296 |
rs144015900 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615458 | GTGCAGAACTCTCGC[G/T]GCTACTAGGGGAGTC | 4296 |
rs144306871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610702 | CCTGTCTCTAGCCAC[C/T]TGTGGCACCCCAGAC | 4296 |
rs144413812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603072 | CATGCCATTGCAGTC[C/T]AGCCTGGGTAACAGA | 4296 |
rs144595056 | snp | C/G | 0.0027462 | 0.0369535 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599525 | CAGATGAGCGGGGAA[C/G]GGGGCGGCTCGGTCG | 4296 |
rs144687659 | snp | A/G | 0.00334125 | 0.0407365 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598564 | GCCCAGGGGTGGTGA[A/G]CGTGGGGTGCCTGGG | 4296 |
rs144723725 | snp | A/G | 1.65831e-05 | 0.00287945 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607974 | TGGGATGGGCAGTGT[A/G]AGCTTGTTAACAGCT | 4296 |
rs144864133 | snp | A/C | 1.65836e-05 | 0.0028795 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605841 | GTGGCTTCGTCCATG[A/C]GGGACCTTCTCCTGG | 4296 |
rs144950486 | snp | A/G | 0.000290692 | 0.0120525 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613049 | ATCACGGTGGATGAC[A/G]GGCACCAGGGCCTCG | 4296 |
rs145124492 | snp | C/T | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608416 | GGGTCTTGTGCTCCA[C/T]GTCGTCACTCTCAAT | 4296 |
rs145141034 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605230 | GAACAGAAAGGCCCC[A/G]AGCTATCCTGGATGT | 4296 |
rs145297254 | snp | G/T | 0.00145306 | 0.0269151 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605778 | TTGAGTGCTGGGGGT[G/T]TGGAAGGAGATCCTA | 4296 |
rs145388794 | snp | C/T | 1.68007e-05 | 0.00289828 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613347 | GCCACCAGCTCACCT[C/T]GCCAGCTGCCCCTGT | 4296 |
rs145992599 | snp | A/G | 2.15892e-05 | 0.00328544 | MAP3K11 | 11 | allele_origin=G(germline)/A(somatic) | 11:65599553 | TCGGGCAGGGCGCGG[A/G]CGTTGGCGTGGGGGG | 4296 |
rs146308898 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610026 | CAGCCATTTCGGCGC[C/T]GGTGCTTCTCAGAGC | 4296 |
rs146321177 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603605 | CCTCTGTGAAGCCCC[A/G]TTATTTGATTCTTAG | 4296 |
rs146665833 | snp | C/T | 0.000126346 | 0.00794713 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613133 | ATGGGGAGGCACGCG[C/T]CGCCCGGCCAGAGCT | 4296 |
rs146745261 | snp | C/T | 0.00022237 | 0.0105421 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599560 | GGGCGCGGGCGTTGG[C/T]GTGGGGGGTGTTGTC | 4296 |
rs146831477 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598002 | CTCCCTGCATCACCC[C/G/T]AGCAGGCAATTCCCT | 4296 |
rs146832985 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608127 | AACCCCCACCCCCTT[A/C]CTGCCACTTCACCCA | 4296 |
rs146966484 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606558 | TCAGAGGTAACAGGC[G/T]AGACCTAAGGCAGGG | 4296 |
rs147094249 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602443 | TTGAGGTCAGGAGTT[C/T]GGGACCAGCCTGGTC | 4296 |
rs147249960 | snp | C/G | 8.33299e-05 | 0.0064543 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607755 | CTGTGCCTCCAGCGC[C/G]TCCAACTGCTGCAGG | 4296 |
rs147313431 | snp | A/G | 1.67911e-05 | 0.00289746 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613601 | CTGCCCACTGGGCTC[A/G]TAGTCGAACAGGGCT | 4296 |
rs147473400 | snp | C/T | 3.31488e-05 | 0.00407103 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607977 | GATGGGCAGTGTGAG[C/T]TTGTTAACAGCTACG | 4296 |
rs147496400 | snp | C/T | 5.28611e-05 | 0.00514079 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613665 | GGAGACCCCTCAGGC[C/T]GGCCTCCTCCACCGC | 4296 |
rs147700629 | snp | C/T | 4.60257e-05 | 0.00479695 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598347 | TGTCTTTGGTCTGTG[C/T]CCTGCAGTCCTGGGG | 4296 |
rs147767445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612656 | GAGCACCAACTCCAC[A/G]AACATGAATTTAGGG | 4296 |
rs147790712 | snp | A/G | 0.000110136 | 0.00741997 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605720 | AAGGTGCCCACGGAA[A/G]GAGCTCAGCCAGATC | 4296 |
rs147829902 | snp | C/T | 8.66789e-05 | 0.0065827 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598565 | CCCAGGGGTGGTGAA[C/T]GTGGGGTGCCTGGGG | 4296 |
rs148137861 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606921 | AGCGGCACGATGGCT[A/G]TGAGACTGTGACCAG | 4296 |
rs148160764 | snp | C/T | 1.75511e-05 | 0.0029623 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605997 | GGACCCCAAGCCCAG[C/T]ATGCTCGCCGCTCTC | 4296 |
rs148368943 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614449 | CCAGATCCCCCATCA[C/T]AGCAGGCTTTTGAGA | 4296 |
rs148528933 | snp | A/G | 5.28788e-05 | 0.00514165 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613666 | GAGACCCCTCAGGCC[A/G]GCCTCCTCCACCGCC | 4296 |
rs148717248 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603368 | GGCGAAACTGCTTCC[A/G]TGAGGTCTCACAGGG | 4296 |
rs148864387 | snp | A/C/T | 0.00026087 | 0.0114178 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598590 | CTGGGGTGCCAGGAG[A/C/T]AGAGCGTGATGTCCC | 4296 |
rs149401275 | snp | C/T | 1.65844e-05 | 0.00287957 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605833 | GGTACCATGTGGCTT[C/T]GTCCATGCGGGACCT | 4296 |
rs149500992 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615445 | GCGTGCTTCGGTAGT[C/G]CAGAACTCTCGCTGC | 4296 |
rs149636495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602911 | CTTAAGCGCAGCCCA[A/G]CCTGGGCAACATGGC | 4296 |
rs149904717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612959 | TAGGCTCAGTGGAAG[A/G]TTGGGAGCAGGTGTG | 4296 |
rs149954894 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605039 | CTTCTGAGCTCACTA[C/T]GAGAGCATTGGAGCT | 4296 |
rs150114594 | in-del | -/GTCTTG | | | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597511 | TTCACCATGTGGCCA[-/GTCTTG]GGTTGAACTCCTGAC | 4296 |
rs150259359 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608941 | CACTCAACCCCAGCA[C/T]TCAAAACCATTTATG | 4296 |
rs150577951 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612040 | GGCTCAAAATATCCA[C/T]GTTGACCCCCCTCTA | 4296 |
rs150628550 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615291 | AGACGACGCTATCCT[A/G]TTTCGACTATTCCTG | 4296 |
rs150927129 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600912 | ACTTAGCTCACAGTC[C/T]CTTCTGTCAGCCCCA | 4296 |
rs151008395 | snp | C/G/T | 0.00354576 | 0.041956 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599503 | GTCGGGCGTCTTGAG[C/G/T]GAGAAGCAGATGAGC | 4296 |
rs151189174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604644 | CCCTCACAGAACTGC[C/T]TGGCACATAGAAGAG | 4296 |
rs181247930 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606983 | ATAAGGAAAGCTACT[C/T]GTCTGAGTCGGAGAT | 4296 |
rs181259966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612775 | ATACCAATTTCTTAA[C/T]TTGTCCAAACCGCAG | 4296 |
rs181380377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601617 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 4296 |
rs181713682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600496 | AAAGGTGGAGCCGGC[C/T]TCACCCCAGGCAAGG | 4296 |
rs182051318 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614539 | CTAAGGATGGGCCAT[C/T]TCTGCCCTCTGCATC | 4296 |
rs182174485 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610842 | TTCTTTGTACTTGTG[A/G]TCTTTCTGCTACCTC | 4296 |
rs182711755 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615799 | CACTGCAGGCTGGCG[A/G]TTCGCGGCTCCTTCT | 4296 |
rs182905791 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610212 | CACCTTTACTATCCC[A/G]GCATGCCCAGTAGAT | 4296 |
rs183221934 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601999 | ACGAGGTCAAGAAAT[C/T]GAGACCATCCTGGCC | 4296 |
rs183292430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602167 | GAGATCCCGCCACTG[C/T]GCTCCAGCCTGGGTG | 4296 |
rs183545948 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615439 | AGAGGGGCGTGCTTC[A/G]GTAGTGCAGAACTCT | 4296 |
rs183896856 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598920 | TAAAAATGGGCATCC[A/G]GGAGCGCTTAGTTCT | 4296 |
rs184052770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609591 | AAAGAGGACAAAGTC[A/T]TAGAGTCATGAAGGG | 4296 |
rs184191950 | snp | C/T | 0.00689342 | 0.0583026 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599353 | CTCCCTGGGAACCCC[C/T]GTCTCCCATATGTGA | 4296 |
rs184680986 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612132 | CTGCTCTCCAGCCTG[C/T]ACTCTGGGCTCTAGG | 4296 |
rs184865291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604165 | TATATGGGCTAATAA[A/G]TAGTTTCTCTTCATA | 4296 |
rs184880571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612820 | CAAGGACTTCTGAAG[C/G]TGGCGCAGGAAGACT | 4296 |
rs184913992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603458 | CAGCGTAGCTGAGTG[C/T]ACCCTGCCAATGTGC | 4296 |
rs184986308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605077 | CTCTGGGTTCAAATC[C/T]TCAGCTGGGGGTTTG | 4296 |
rs185137040 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608812 | GTAGAGACAGGGTTT[C/G]TCCATGTTGGTCAGG | 4296 |
rs185795382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601891 | GTTTAAACAGAAGAG[A/G]GGAAATCATGTTTAA | 4296 |
rs185854808 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611817 | GGAATCCCCCTCAGA[A/C/T]TGGGGCAGGTAGCGG | 4296 |
rs186187308 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615475 | CTACTAGGGGAGTCC[A/G]CGCCTCCACCTTTTC | 4296 |
rs186572828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610031 | ATTTCGGCGCTGGTG[C/T]TTCTCAGAGCATGAC | 4296 |
rs186746836 | snp | G/T | 0.0345662 | 0.12684 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607431 | CACTGGGCCAGCAGG[G/T]GCTCGCGCCGCCGCA | 4296 |
rs186806089 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611023 | TGGGCCAGAGACCCC[A/G]AAACTGGGGGAAGCT | 4296 |
rs187037562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600506 | CCGGCCTCACCCCAG[G/T]CAAGGGCAGTAGAAC | 4296 |
rs187307283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610747 | TCCAGTATCTCAGGC[C/T]GGGTGGCCACTCTCC | 4296 |
rs187335911 | snp | A/G | 0.0107246 | 0.0724382 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597494 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTGGC | 4296 |
rs187592646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603500 | GCCAGCTCTCCAGGG[A/G]CCAGAACAGCCCACT | 4296 |
rs187594850 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615082 | CTGCACCTCAAGCTC[G/T]TGGAGTGGATTGCCT | 4296 |
rs187861496 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602097 | AGTCTCAGCTACTTG[G/T]GAGGCTGAGGCAGGA | 4296 |
rs188061400 | snp | C/G | 5.06103e-05 | 0.00503017 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607822 | GCCCAGCAGTCTAGG[C/G]GCACGGCGTGCAGCG | 4296 |
rs188112562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599020 | CCAGGAGTTTGCTAC[A/G]ATTATGATTACATGT | 4296 |
rs188186435 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613843 | CCAAGGCCCTAGTCC[C/T]GGAACCTGGGCATCC | 4296 |
rs188410172 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612195 | GGTCCTGCTTCCATG[C/G]CTTCTCTCTCTAAAT | 4296 |
rs188735936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602718 | GAGGCTGAGGGAGAA[C/T]TGCTTGAACGTGGGA | 4296 |
rs188999003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600257 | TCAACTCTAAGGTAC[A/G]TGGCAGCCCTGAGGG | 4296 |
rs189340469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604230 | GGGCAAGCTTGAGAA[C/T]GATGGGGCCCAGGCC | 4296 |
rs189877999 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601985 | AAGGTGGGCGGATCA[C/G]GAGGTCAAGAAATCG | 4296 |
rs189978729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611926 | AGGATGGTTGGCAGG[A/C]CTCTCCTGGCTCCCC | 4296 |
rs190060684 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615604 | CCTGGGTTGGCAACG[A/C]CTGGGTCTACGCATG | 4296 |
rs190282541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605086 | CAAATCCTCAGCTGG[C/G]GGTTTGAGGTAGGTT | 4296 |
rs190434670 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602151 | GAGGTTACAGTGAGC[C/G]GAGATCCCGCCACTG | 4296 |
rs190771461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609199 | TGTTGAGGCAGGAGC[A/G]TGAATCAGAACCCCC | 4296 |
rs191073023 | snp | A/G | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600928 | CTTCTGTCAGCCCCA[A/G]CCCTTACTCAGACTC | 4296 |
rs191524877 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615273 | AGCCTGTCACTTTAA[C/G]AAAGACGACGCTATC | 4296 |
rs191545774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603809 | CACTGGTGTTGAGGC[C/T]GACATACTTATCAAG | 4296 |
rs191843021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610775 | TCCACCTTTTTCAGG[C/T]GGGGAATCTGAGGCC | 4296 |
rs192038350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610075 | CTGCCCACTGCCCCT[C/G]GCTGACTCAGCCTCT | 4296 |
rs192284959 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598191 | GGGTGGGGTCCCTGG[A/G]GAAACTGAGGCAGCT | 4296 |
rs192530900 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602760 | AAGTGAGCTGAGGTC[A/G]CACCACTGCACTCCA | 4296 |
rs192588436 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604563 | CTGGTTGCCTTACAT[C/G]AAACCACTTAATCTC | 4296 |
rs192939587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599159 | ACCACTGCCTGGCCC[A/G]ATTACTTCTTTTATT | 4296 |
rs193020866 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611581 | CAGGCTCCTTCCTCC[C/T]GCAAGTCCTCCACCC | 4296 |
rs193181574 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612093 | TGACCACACTGAGCC[C/T]GGCCCCTCCTGCATT | 4296 |
rs199497456 | snp | A/G | 3.36564e-05 | 0.00410208 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613273 | GCCGGGCCTCCTGGC[A/G]AACGCTCTCGGCTGT | 4296 |
rs199572841 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601572 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 4296 |
rs199601318 | snp | A/T | 0.000464306 | 0.0152295 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605813 | GGATGAGTCATCTGA[A/T]TCCAGGTACCATGTG | 4296 |
rs199635742 | snp | A/G | 9.05264e-05 | 0.00672718 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599669 | GTGCCGCGCAGCAGC[A/G]CCCGCTGGATCAGCT | 4296 |
rs199701635 | in-del | -/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598172 | TTCCTGACCCCCAAA[-/G]GGGGGGTGGGGTCCC | 4296 |
rs199757732 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614692 | CTTTCTTTTTTCTTC[C/T]TTTGAGACGGAGTCT | 4296 |
rs199769348 | snp | A/G | 0.00107031 | 0.0231086 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599561 | GGCGCGGGCGTTGGC[A/G]TGGGGGGTGTTGTCG | 4296 |
rs199933724 | snp | C/T | 0.000316713 | 0.01258 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613693 | CGCCCCCACCACCCC[C/T]GCTGCCACTGCCATT | 4296 |
rs199974953 | in-del | -/CGG | | | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608373 | GTTTTGTGCCACTCT[-/CGG]GCCAGGCCAAAGTCG | 4296 |
rs200098330 | snp | C/T | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598468 | TGGTGATGGCAGGGG[C/T]GAAGGCCGTGGCCCA | 4296 |
rs200329338 | snp | A/C | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613676 | AGGCCGGCCTCCTCC[A/C]CCGCCCCCACCACCC | 4296 |
rs200559405 | snp | C/T | 3.30715e-05 | 0.00406628 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608086 | CTGTGGGCGAGACAA[C/T]AGGTCTGTGTTCCCT | 4296 |
rs200573862 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611650 | GGGAGCAGGGGCTGG[A/G]GCAGGGACAGGAAGC | 4296 |
rs200642724 | snp | C/T | 0.00180069 | 0.0299517 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613398 | ATGCCGATCACCTCC[C/T]CCAGCCGCAGCTCCT | 4296 |
rs200790570 | snp | A/G | 0.00425703 | 0.045939 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599816 | GCTGGTGCATATTCC[A/G]GGTGAGGGCCCAAGA | 4296 |
rs201108277 | snp | A/G | 0.000353728 | 0.0132943 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599547 | GCTCGGTCGGGCAGG[A/G]CGCGGGCGTTGGCGT | 4296 |
rs201216651 | in-del | -/G | | | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597306 | GGCCTATGGTTTTTT[-/G]TTTTTTTTTTTTTTG | 4296 |
rs201233315 | snp | A/C | 3.63286e-05 | 0.00426181 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613013 | CCATGCCCCCAGAAA[A/C]TCACTGTTGTTGGAC | 4296 |
rs201421272 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614691 | TCTTTCTTTTTTCTT[C/T]TTTTGAGACGGAGTC | 4296 |
rs201471095 | snp | G/T | 1.68883e-05 | 0.00290584 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613467 | CGAGACACATAGTTG[G/T]ACGGGAAGATGCCCA | 4296 |
rs201522259 | snp | A/G | 0.0010802 | 0.0232149 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599397 | CAGGCCACTCACCGC[A/G]GGGCTCCTCCTCACG | 4296 |
rs201560004 | snp | A/G | 0.00697555 | 0.058644 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599566 | GGGCGTTGGCGTGGG[A/G]GGTGTTGTCGGGGAC | 4296 |
rs201727045 | snp | A/G/T | 7.27809e-05 | 0.00603209 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599483 | GGTGCAGGAGTGGGC[A/G/T]GGGAGTCGGGCGTCT | 4296 |
rs201795936 | snp | G/T | 0.00297176 | 0.0384324 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608472 | GAGGGGCCAGATTGT[G/T]GATGCTCCAGGATCA | 4296 |
rs201949210 | snp | C/T | 3.34666e-05 | 0.0040905 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605777 | ATTGAGTGCTGGGGG[C/T]GTGGAAGGAGATCCT | 4296 |
rs202041637 | snp | A/G | 0.000131315 | 0.00810185 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599783 | CCTGCGGGCAGAGGC[A/G]GCACAGGTGAGGGTG | 4296 |
rs202052634 | snp | C/T | 0.000321627 | 0.0126772 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599394 | CTTCAGGCCACTCAC[C/T]GCGGGGCTCCTCCTC | 4296 |
rs202055993 | snp | C/T | 0.000438418 | 0.0147992 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613770 | ATGGCCGGGAGCCGG[C/T]GCTGGGATGTGTGGA | 4296 |
rs202150507 | snp | G/T | 0.000652649 | 0.0180527 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605912 | CTTGGGGAAAGCAAA[G/T]GATGCTGGGTCTGGG | 4296 |
rs367624099 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606430 | AATAACTACCAAATA[C/G]AATTATTGCAAGAAA | 4296 |
rs367682909 | snp | C/T | 0.00072102 | 0.0189734 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599772 | GCGGGGGGTTACCTG[C/T]GGGCAGAGGCGGCAC | 4296 |
rs367882937 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609655 | CAACTGCACTGTGGA[A/T]GAGAAGCAATATCAA | 4296 |
rs367920151 | snp | C/T | 0.000307953 | 0.0124049 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613560 | AGCACCTCCACACGG[C/T]CACCCTTCCTCAGGG | 4296 |
rs368085716 | snp | A/G | 1.68349e-05 | 0.00290123 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607938 | GGCCATAAGCTGTGC[A/G]AAGGGCTCGGGGCAG | 4296 |
rs368115877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600006 | AAAGCCCAATGGCAG[C/T]CAGCGACCCCAGACC | 4296 |
rs368138317 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65616245 | TCAGGCGCCAGACGG[A/G]GCATGGGCCGGGGGC | 4296 |
rs368245376 | snp | A/C/G | 5.73415e-05 | 0.00535425 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606074 | CTGGCCTGGCTCTGC[A/C/G]GGCTCCACTGCAGGG | 4296 |
rs368386071 | in-del | -/CA | 0.029116 | 0.117091 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603947 | GGGCTGCGGCTCTCT[-/CA]GTTTGCAGGGGCTGG | 4296 |
rs368386691 | snp | C/G/T | 5.06234e-05 | 0.00503086 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613532 | GTCTCCTGAGATGGC[C/G/T]GCGTCCCGGGACAGC | 4296 |
rs368488158 | snp | A/G | 8.71665e-05 | 0.00660119 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605744 | CCAGATCCTGCCGGG[A/G]GAGGAAGGCCACTCA | 4296 |
rs368536767 | snp | A/G | 0.000128524 | 0.00801532 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599551 | GGTCGGGCAGGGCGC[A/G]GGCGTTGGCGTGGGG | 4296 |
rs368669140 | snp | A/G | 3.69454e-05 | 0.00429783 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605716 | CCCCAAGGTGCCCAC[A/G]GAAGGAGCTCAGCCA | 4296 |
rs368733999 | snp | G/T | 3.10525e-05 | 0.00394022 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598323 | GCACCCACGGGGCCT[G/T]GGCACCCATGTCTTT | 4296 |
rs368776174 | snp | C/G | 1.70606e-05 | 0.00292062 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607884 | TGTGTCCTGGGCCAG[C/G]GAGCTCTGTACCTCA | 4296 |
rs368967593 | snp | A/G | 1.6638e-05 | 0.00288422 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607962 | GGGGCAGGTGGATGG[A/G]ATGGGCAGTGTGAGC | 4296 |
rs369239714 | snp | C/T | 3.96644e-05 | 0.00445316 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599396 | TCAGGCCACTCACCG[C/T]GGGGCTCCTCCTCAC | 4296 |
rs369320586 | in-del | -/GGGAATGGAAGAGGC | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604704 | ATCAAGTGTAGCTCA[-/GGGAATGGAAGAGGC]GGGAATGGAAGAGGC | 4296 |
rs369813259 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601124 | GCCTTGGCCCCTGTC[C/G]GCAGCCCCAGTCCTG | 4296 |
rs369918473 | snp | C/T | 0.000334431 | 0.0129269 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605908 | AGGACTTGGGGAAAG[C/T]AAATGATGCTGGGTC | 4296 |
rs370002899 | snp | A/C/T | 0.000271201 | 0.0116419 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598315 | CGCTTCCGGCACCCA[A/C/T]GGGGCCTGGGCACCC | 4296 |
rs370003710 | snp | C/T | 1.65784e-05 | 0.00287905 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608120 | CTCTCCCAACCCCCA[C/T]CCCCTTACTGCCACT | 4296 |
rs370036394 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612278 | TGATGGGCAGCGTGT[C/T]GGGGGCTTGAAATGA | 4296 |
rs370191446 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597538 | TGACCTCATGTGATC[C/T]GCCGGCCTCGGCCTC | 4296 |
rs370229386 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604878 | CCCACAGGCAAGGGA[A/G]GCCATAACTCTCTGG | 4296 |
rs370241046 | snp | A/G | 1.79107e-05 | 0.0029925 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613187 | ATACTCCATCACCAG[A/G]CACAGGTTGGGCTCC | 4296 |
rs370285652 | snp | C/T | 7.38975e-05 | 0.0060781 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598408 | GTCCCAGAAGGGGTC[C/T]GAGTCCGGGAACAAG | 4296 |
rs370331573 | snp | A/G | 0.000144587 | 0.00850133 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599609 | CGTCCTGGGCCTCCC[A/G]GCGGCTGCAGGTCGC | 4296 |
rs370453545 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601332 | AAGCCCTCCCAGAAT[C/T]TCCCTGAACCTACAC | 4296 |
rs370501486 | snp | A/G | 0.000309952 | 0.0124451 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599491 | AGTGGGCGGGGAGTC[A/G]GGCGTCTTGAGCGAG | 4296 |
rs370781399 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615608 | GGTTGGCAACGCCTG[A/G/T]GTCTACGCATGCGCC | 4296 |
rs370906433 | snp | C/T | 0.000437666 | 0.0147865 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605931 | GCTGGGTCTGGGGGG[C/T]ACTCAGGTACTCACC | 4296 |
rs370949160 | in-del | -/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604496 | GCAGATGGAGGCCCA[-/G]GGCTCTGCCTCTGTG | 4296 |
rs371116061 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599839 | GCCCAAGACCTCTCC[A/G]TGGTCTTGGAACAAG | 4296 |
rs371379749 | snp | G/T | 1.67427e-05 | 0.00289328 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613320 | TCGGGGTCCTGGCGA[G/T]CTGCCTTCACAGCCA | 4296 |
rs371575835 | snp | A/C | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608003 | CTACGCCATAGGCCA[A/C]AGCAAGGCAGTCAAT | 4296 |
rs371667653 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600923 | AGTCCCTTCTGTCAG[A/C]CCCAACCCTTACTCA | 4296 |
rs371677177 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614144 | GGTCTTTTTGCGCAG[G/T]GGGTGGAGGGAGCGT | 4296 |
rs371729065 | snp | C/T | 0.00030215 | 0.0122875 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613600 | CCTGCCCACTGGGCT[C/T]GTAGTCGAACAGGGC | 4296 |
rs371854714 | snp | A/C | 3.35627e-05 | 0.00409637 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607944 | AAGCTGTGCGAAGGG[A/C]TCGGGGCAGGTGGAT | 4296 |
rs372066843 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607911 | CTCACCTGCCCTCCC[C/T]GTCCTCTTACCGGCC | 4296 |
rs372241785 | snp | A/G | 0.000154636 | 0.00879171 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599559 | AGGGCGCGGGCGTTG[A/G]CGTGGGGGGTGTTGT | 4296 |
rs372293005 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607171 | CACGGGCCCACCCAC[A/G]ACACCCTAAACCAAT | 4296 |
rs372545474 | snp | C/G | 0.000179429 | 0.00947006 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598592 | GGGGTGCCAGGAGCA[C/G]AGCGTGATGTCCCCG | 4296 |
rs372958068 | snp | A/G | 9.07812e-05 | 0.00673664 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613087 | GGTAGTGCATCCCAC[A/G]GGCAATCTGCACAGC | 4296 |
rs372990230 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601334 | GCCCTCCCAGAATCT[C/T]CCTGAACCTACACAG | 4296 |
rs373143339 | snp | A/C/T | 3.76244e-05 | 0.00433714 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599414 | GGCTCCTCCTCACGT[A/C/T]GGGGGCTCTTGGCTG | 4296 |
rs373181468 | snp | C/T | 1.68479e-05 | 0.00290236 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608253 | CAGCCCGTCCAGCCC[C/T]ACCAAGGGCCGCACC | 4296 |
rs373301926 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605866 | TCCTGGTGATGGGAG[A/G]GCAAGGAGGGGTGCT | 4296 |
rs373432376 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615267 | GCTTTGAGCCTGTCA[C/T]TTTAAGAAAGACGAC | 4296 |
rs373571525 | snp | C/T | 5.29021e-05 | 0.00514279 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606003 | CAAGCCCAGCATGCT[C/T]GCCGCTCTCCATTGC | 4296 |
rs373649447 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598448 | GCTCGGCGGGGTGCA[A/G]GCTGTGGTGATGGCA | 4296 |
rs373717045 | snp | A/G | 7.39098e-05 | 0.00607861 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598316 | GCTTCCGGCACCCAC[A/G]GGGCCTGGGCACCCA | 4296 |
rs373743021 | snp | C/G/T | 0.000799972 | 0.0199859 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606820 | CTGGGATTTGGGTTG[C/G/T]GGGGAGCAGGGTTCA | 4296 |
rs373978204 | snp | A/C/G | 9.19099e-05 | 0.00677846 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606854 | TTGTGATGAAGTAGA[A/C/G]CCAGGACCCCAACCT | 4296 |
rs374000482 | snp | A/G | 5.99682e-05 | 0.00547545 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607349 | GCGGCGGCGGCGCAC[A/G]TGCGGTCGCTCGCGG | 4296 |
rs374018444 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598226 | AGGCTGACCCAGCTC[C/T]TGTTCCAGTGTATGC | 4296 |
rs374217526 | snp | A/C/T | 1.68562e-05 | 0.00290307 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613272 | AGCCGGGCCTCCTGG[A/C/T]GAACGCTCTCGGCTG | 4296 |
rs374223116 | snp | A/G | 3.71872e-05 | 0.00431187 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599508 | GCGTCTTGAGCGAGA[A/G]GCAGATGAGCGGGGA | 4296 |
rs374278910 | snp | A/G | 3.37775e-05 | 0.00410945 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613517 | CGCCCACCAGCCCTC[A/G]TCTCCTGAGATGGCT | 4296 |
rs374403231 | snp | A/G | 0.000358576 | 0.013385 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599773 | CGGGGGGTTACCTGC[A/G]GGCAGAGGCGGCACA | 4296 |
rs374422083 | snp | C/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613441 | CCTCGCAGGGGGGCG[C/G]GCCGCCACCCCGAGA | 4296 |
rs374511571 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606373 | GTGTAACAAGTTACT[G/T]TTTTCACTTTTCTCA | 4296 |
rs374524526 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606985 | AAGGAAAGCTACTCG[C/T]CTGAGTCGGAGATGC | 4296 |
rs374573657 | snp | A/G | 0.000157988 | 0.00888644 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599549 | TCGGTCGGGCAGGGC[A/G]CGGGCGTTGGCGTGG | 4296 |
rs374598892 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599323 | TCCTTGCATGTCCCC[A/C]CCAGCCACTCCTCCC | 4296 |
rs374611372 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607750 | AGGACCTGTGCCTCC[A/G]GCGCCTCCAACTGCT | 4296 |
rs374614823 | in-del | -/CATCT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601096 | ATTCAATCAACATCT[-/CATCT]ACTGACCCATGTGCC | 4296 |
rs374807465 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609037 | TCATACAACAAATAC[A/C]GCAGAGATTACAACC | 4296 |
rs375011164 | snp | A/G | 2.19691e-05 | 0.00331422 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599377 | TATGTGAAGCAGGCC[A/G]GCTTCAGGCCACTCA | 4296 |
rs375059424 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615635 | CGCCCAAACGCTTTT[A/C]CGCTCGAACTTGCTT | 4296 |
rs375059468 | snp | A/T | 8.50724e-05 | 0.00652142 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607916 | CTGCCCTCCCCGTCC[A/T]CTTACCGGCCATAAG | 4296 |
rs375349799 | snp | C/T | 3.31835e-05 | 0.00407316 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605810 | GGGGGATGAGTCATC[C/T]GAATCCAGGTACCAT | 4296 |
rs375370224 | snp | A/G | 0.000236084 | 0.0108621 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613540 | AGATGGCTGCGTCCC[A/G]GGACAGCACCTCCAC | 4296 |
rs375374920 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614156 | CAGGGGGTGGAGGGA[A/G]CGTCCGCAGTTGGGC | 4296 |
rs375614171 | snp | A/G | 0.000141051 | 0.00839677 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598440 | TCCAGGGTGCTCGGC[A/G]GGGTGCAGGCTGTGG | 4296 |
rs375659011 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614967 | GGCGTGAGCCACCGC[A/G]CCCGGCCATTCTTTT | 4296 |
rs375780436 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611092 | ACCTGGCCACCAGCT[C/G]CCTCCCTGGGCTGGC | 4296 |
rs375814282 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607714 | TGCATGGAATGGAAG[A/G]AGTCCCGCGGCATTT | 4296 |
rs375853883 | snp | A/C | 1.85779e-05 | 0.00304772 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599420 | TCCTCACGTCGGGGG[A/C]TCTTGGCTGACCGCT | 4296 |
rs375868706 | snp | C/G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605059 | GCATTGGAGCTGAAG[C/G/T]CTCTCTGGGTTCAAA | 4296 |
rs375938376 | snp | C/G | 0.000132107 | 0.00812626 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608034 | GCCACGGTATGGCAC[C/G]TCCCCGGTCAGCAGT | 4296 |
rs376103936 | snp | A/G | 1.86111e-05 | 0.00305044 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599509 | CGTCTTGAGCGAGAA[A/G]CAGATGAGCGGGGAA | 4296 |
rs376132828 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599121 | CACGTGATCCTCCCA[A/G]AGTGCTGGGATCACA | 4296 |
rs376240928 | snp | C/T | 3.47772e-05 | 0.00416982 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599739 | GCCTCTTGGGCTCCT[C/T]GGGCTCCAGGCTAGG | 4296 |
rs376244842 | snp | A/G | 3.62601e-05 | 0.00425779 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606037 | AGTCCTCCAGACGTC[A/G]GGGGGACTGGCGGCC | 4296 |
rs376338840 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615598 | GTCTACCCTGGGTTG[A/G]CAACGCCTGGGTCTA | 4296 |
rs376567112 | snp | C/G/T | 5.07544e-05 | 0.00503737 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606654 | GAGAATAAGGAGCTG[C/G/T]GGGGCGGAGAGGGGC | 4296 |
rs376714195 | snp | A/G | 0.000146188 | 0.00854826 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598596 | TGCCAGGAGCAGAGC[A/G]TGATGTCCCCGGTGG | 4296 |
rs376777285 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603356 | AGATAGATAGAGGCG[-/A]AAACTGCTTCCGTGA | 4296 |
rs376790642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602465 | AGCCTGGTCAACATG[A/G]TGAAACCTCATCTCT | 4296 |
rs376825039 | snp | A/G | 5.01584e-05 | 0.00500766 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607949 | GTGCGAAGGGCTCGG[A/G]GCAGGTGGATGGGAT | 4296 |
rs377000140 | snp | A/C/G | 3.34595e-05 | 0.00409009 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613304 | CACACTGATGTCCTC[A/C/G]TCGGGGTCCTGGCGA | 4296 |
rs377030693 | in-del | -/TG | 0.02016 | 0.0983543 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609298 | GTGCCCACATCACAC[-/TG]TGGCAAGTGCAGCCA | 4296 |
rs377128459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601216 | TGAGCTGCATGCCTG[C/T]GCACACACTATTCAC | 4296 |
rs377291303 | in-del | -/TCT | | | upstream-variant-2KB, cds-indel, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615111 | CTAAGGCTCTCTTCT[-/TCT]CCTCACCTGGGAAAC | 4296 |
rs377483098 | snp | A/G/T | 0.000100911 | 0.00710261 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605925 | AATGATGCTGGGTCT[A/G/T]GGGGGCACTCAGGTA | 4296 |
rs377509272 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605541 | TGAGACTCTGGGCCC[C/T]GAGCCGAGGCCTGGG | 4296 |
rs377553569 | snp | C/T | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599406 | CACCGCGGGGCTCCT[C/T]CTCACGTCGGGGGCT | 4296 |
rs377564375 | snp | C/T | 7.74338e-05 | 0.00622181 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599401 | CCACTCACCGCGGGG[C/T]TCCTCCTCACGTCGG | 4296 |
rs377632475 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602564 | GGCAGGAGAATCACT[C/T]GAACCTGGGAGGTGG | 4296 |
rs377697446 | snp | A/G | 0.000133643 | 0.00817335 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605904 | TTTCAGGACTTGGGG[A/G]AAGCAAATGATGCTG | 4296 |
rs386754391 | multinucleotide-polymorphism | CTC/TTT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601332 | AAGCCCTCCCAGAAT[CTC/TTT]CCTGAACCTACACAG | 4296 |
rs386754392 | in-del | ATGGGCTGGGTGG/GGAATGGAAGAGGC | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604721 | GGAATGGAAGAGGCG[ATGGGCTGGGTGG/GGAATGGAAGAGGC]GATGGGAGGAGTGAG | 4296 |
rs397695136 | in-del | -/T | 0 | 0 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601832 | CCACGAGGTTATCAT[-/T]ATCACCCCCACTTCG | 4296 |
rs397849657 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602204 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 4296 |
rs527426586 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612865 | GGGCTCTGTTTGGGG[A/G]CTAGCTTGAGCCCAT | 4296 |
rs527429690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604479 | GAGTAGCAAATGGCG[A/G]GGCAGATGGAGGCCC | 4296 |
rs527747248 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597917 | CCTAGGGCAGGGGCC[A/G]CAGTAGCAGGACTTG | 4296 |
rs528038802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599150 | CAGGCGTGCACCACT[A/G]CCTGGCCCGATTACT | 4296 |
rs528040778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606206 | CATTCCCAGGGTGAG[C/G]TTTGGGCAAGATAGA | 4296 |
rs528347623 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615130 | CTCACCTGGGAAACA[A/G]TCCGCTTCTTCATAT | 4296 |
rs528612027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600974 | ACCCAACTCCCACCC[C/T]GGCCACTGCCACTGA | 4296 |
rs528737223 | snp | C/T | 0.000185979 | 0.00964131 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613502 | GCCACCCACCTGGCC[C/T]GCCCACCAGCCCTCG | 4296 |
rs528821029 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615451 | TTCGGTAGTGCAGAA[C/G/T]TCTCGCTGCTACTAG | 4296 |
rs528847530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602698 | CTGTAATCCCAGCTA[C/T]TGGGGAGGCTGAGGG | 4296 |
rs529043415 | in-del | -/CTTTCGTGAACCCCACCCCTTCCCACTCCCAGAC | 0.00358779 | 0.0422022 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607041 | TAGACCTTCCCAGAA[lengthTooLong]CGACATGCAAATACT | 4296 |
rs529110179 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601441 | GGGCAGTGTTTAACA[A/T]GTTGATGCCTGGCTC | 4296 |
rs529412589 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597587 | AGGAGTGAGCCACTG[C/T]ACCTGGCCGAGAAGA | 4296 |
rs529464475 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604577 | TCAAACCACTTAATC[A/T]CTCTGTGCCTCAGTT | 4296 |
rs529598264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611946 | CCTGGCTCCCCCAGT[C/T]CTGGCAAGAACTTGG | 4296 |
rs530354487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600011 | CCAATGGCAGCCAGC[A/G]ACCCCAGACCCGAAA | 4296 |
rs530498776 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615700 | CCTCGCGTCCTACCG[C/T]GCCATCACCTTTCTG | 4296 |
rs530581552 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605220 | CCGTCATGGAGAACA[A/G]AAAGGCCCCGAGCTA | 4296 |
rs530869395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608195 | CTGGACTTGGCCCAG[C/G]CCTAGATTTAGGCAG | 4296 |
rs531047902 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611931 | GGTTGGCAGGCCTCT[C/T]CTGGCTCCCCCAGTC | 4296 |
rs531214577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603588 | TCTCACAGGGTCTGG[A/G]ACCTCTGTGAAGCCC | 4296 |
rs531346363 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610783 | TTTCAGGTGGGGAAT[A/C]TGAGGCCCAGAGAGG | 4296 |
rs531477216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602734 | TGCTTGAACGTGGGA[A/G]GTGGAGGCTGAAGTG | 4296 |
rs531663136 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597313 | GGTTTTTTGTTTTTT[G/T]TTTTTTTGAGACGGA | 4296 |
rs531817175 | snp | C/T | 9.32879e-05 | 0.006829 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598615 | TGTCCCCGGTGGGGG[C/T]GAGACAGTGCCTCCT | 4296 |
rs531901744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599077 | AGTGTCATGATCACC[A/G]CTCACTGCAGCCTCA | 4296 |
rs531946259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605666 | AGAGCAACCAGGGCA[A/G]GACTCCTGCTTTGCC | 4296 |
rs532341547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600954 | GACTCTCTGCCTCTT[A/G]CCTCACCCAACTCCC | 4296 |
rs532515949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607008 | GGAGATGCCCTGGCG[C/T]CGGCCGGCCCCGCCC | 4296 |
rs532546070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600210 | CTGCCCACCCACCCC[C/T]GCTCCAGCTGTAGCT | 4296 |
rs532939617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609122 | AGCAAAACTGGCAAG[C/G]TGGCAGCTCTGGACA | 4296 |
rs532976710 | snp | C/T | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608422 | TGTGCTCCATGTCGT[C/T]ACTCTCAATGGGCTG | 4296 |
rs533001054 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615789 | GCGCATGCGCCACTG[C/G]AGGCTGGCGGTTCGC | 4296 |
rs533152628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600922 | CAGTCCCTTCTGTCA[A/G]CCCCAACCCTTACTC | 4296 |
rs533168444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602533 | TGCCTGTAATCCCTG[C/T]TACTTGGGAGGCTGA | 4296 |
rs533311731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601931 | AGAGTTGGCCGGGTG[C/T]GGTGGCTCACACCTG | 4296 |
rs533782756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611129 | GGGGCTTGGGAGTGG[C/T]CTGGGCAGCTCACAC | 4296 |
rs533988425 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612239 | GGAAACCCTCTGAAG[C/G]TGTCACTCACTTCTC | 4296 |
rs534207386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605226 | TGGAGAACAGAAAGG[C/T]CCCGAGCTATCCTGG | 4296 |
rs534209571 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597761 | CAGGCTACATGTGGG[A/G]AGACAGCTTTTGAGT | 4296 |
rs534245576 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604725 | TGGAAGAGGCGATGG[A/G]CTGGGTGGGATGGGA | 4296 |
rs534300971 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614260 | TTTGTACTTTGGCCC[C/T]GGGGGCGGGAGGCAG | 4296 |
rs534449343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601890 | AGTTTAAACAGAAGA[C/G]GGGAAATCATGTTTA | 4296 |
rs534883325 | snp | C/T | 0.000117325 | 0.00765824 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608468 | AGAAGAGGGGCCAGA[C/T]TGTGGATGCTCCAGG | 4296 |
rs535083410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610652 | GTGCCAGGGCCCACC[C/T]TCCCCTTTGAAGACC | 4296 |
rs535233157 | snp | C/T | 1.97112e-05 | 0.0031393 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607505 | CTCCTCCTCGCGGCT[C/T]AGTAGTTCCTGCGCC | 4296 |
rs535287370 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599203 | CGCCCCCACCTGCCT[A/G/T]GACCACCTGATAGCT | 4296 |
rs535818553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610939 | TTTCAACTGTCCCAA[C/T]TCGAACTGCTGTTCT | 4296 |
rs536097610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612384 | AGCCCTCAAATGTCC[A/G]TCTCCATGGCTGAGG | 4296 |
rs536153978 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602865 | CACACCTGTAATGCC[A/G]GCACTTTGGGAGGCT | 4296 |
rs536184777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603906 | TCTGCAATTTCATAT[C/T]GTGGGAGCATTCACT | 4296 |
rs536253412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599299 | GATGACTGTGGTCTC[A/G]GCCTTGCCTCCTTGC | 4296 |
rs536427318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605276 | TGGATCCTGCCTGCT[C/T]GGCCTTCTCATTCTC | 4296 |
rs536622736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607192 | CTAAACCAATCCCAG[C/T]GCGGTGAGCACACAG | 4296 |
rs536831818 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613817 | CCCGTGGTCCCCACC[C/G]CCGCTGGCTGCCAAG | 4296 |
rs537066174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606596 | GGGCGGGGAGGAAGA[A/G]GGGATAGTGAGTGGG | 4296 |
rs537180579 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611688 | GGGGCAGCAGGAAAC[A/G]CAGGAAGCAGTGGGG | 4296 |
rs537227664 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602135 | TTGAACCCAGGAGGC[A/G]GAGGTTACAGTGAGC | 4296 |
rs537306605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608612 | GTCAGACATTTCTTT[C/T]CTTTTCCTTTTTTTT | 4296 |
rs537671689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601573 | CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 4296 |
rs538226088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604646 | CTCACAGAACTGCTT[C/G]GCACATAGAAGAGAA | 4296 |
rs538241023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612887 | TGAGCCCATGGGCAC[C/T]CCTGGTCAGCTGGGA | 4296 |
rs538262640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604124 | AATTACTTAGAAGTT[A/T]GTCACTGATCTGAAC | 4296 |
rs538301615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611041 | ACTGGGGGAAGCTCT[C/T]AGTGCCCCTTTAGGG | 4296 |
rs538502179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605453 | TCTTTTCTCCCTGGA[A/G]CCTGCTAAAGGCACA | 4296 |
rs538857234 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615390 | GCGAAATCGGTCGTG[A/T]CGTACGAGGTCCAGC | 4296 |
rs539256941 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614703 | CTTCTTTTGAGACGG[A/C]GTCTTGCTCTGTCGC | 4296 |
rs539424730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601353 | GAACCTACACAGTTA[C/T]TGCTCACGTTATGCC | 4296 |
rs539463184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600685 | TGGGCTCTCACAAGC[C/T]CTGATTTTGTCAGAT | 4296 |
rs539502369 | snp | C/G | 0.000650689 | 0.0180256 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607361 | CACGTGCGGTCGCTC[C/G]CGGTCCACCTGCTGC | 4296 |
rs539667100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602958 | AAAAAATATAAAAAT[C/T]AGCCAAGCATGGCAT | 4296 |
rs539706133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602302 | AGATCACTTGAGGTC[A/C]GGAGTGCATGACTAG | 4296 |
rs540058387 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603046 | AGGCAGAGTTTGCAG[C/T]GAGCCATGATCATGC | 4296 |
rs540088401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610377 | GAGCATGAAACAAGA[C/T]CACACTTTTAAAGTT | 4296 |
rs540482803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602581 | AACCTGGGAGGTGGA[A/G]GTTGTAGTGAGCCGA | 4296 |
rs540496232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611893 | AACCGCACCCTACCA[A/G]GGATGAGAAGAGTGG | 4296 |
rs540524700 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603867 | TTTCATGAAACCTCA[C/G]ACATGTGGCCTTCTG | 4296 |
rs540568621 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608639 | TTTTTTTCTTAAGAT[-/A]AGAGTTTTGCTCTTG | 4296 |
rs540676201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604899 | AACTCTCTGGCCTCA[C/G]TCAGAGCTGGGCAGT | 4296 |
rs540721329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612942 | TGCAGTAGACCCTAA[A/G]CTAGGCTCAGTGGAA | 4296 |
rs540810612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612495 | AATTGAGGCTCCGAG[G/T]TGGAGTAACCAGCTA | 4296 |
rs541054631 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614873 | AGTGGAGACGGGTTT[C/T]ACCATGTTGGCCATG | 4296 |
rs541315313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606916 | TAGGGAGCGGCACGA[G/T]GGCTGTGAGACTGTG | 4296 |
rs541408886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606217 | TGAGCTTTGGGCAAG[A/G]TAGATGGGTTTGGGT | 4296 |
rs541445862 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614039 | AGGGACCCGAGCTTC[C/T]CTCGGTTCTGGAGCA | 4296 |
rs541541510 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603289 | CCTGGCAGCAAGAGT[C/T]AGCAACTCTGTTGTT | 4296 |
rs541653267 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608909 | GCCACTGCACCTGGC[C/T]GAGGCCAAACATTTC | 4296 |
rs542224766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602385 | GCATGGTGGTTCACG[C/T]TTGTAATCCCAGCAC | 4296 |
rs542251581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603564 | TGGTATGGCTTATGC[C/T]GGGGACCATCTCACA | 4296 |
rs542263578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609770 | GGGCACAGGGGGTGG[A/G]GCAGATGGGAAGGGC | 4296 |
rs542288260 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610773 | TCTCCACCTTTTTCA[C/G]GTGGGGAATCTGAGG | 4296 |
rs542452587 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600463 | GTTGAGGGCTTGTGC[A/G]GAGCTGTACAGCCAG | 4296 |
rs542492766 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598786 | GTGCCTCTGTTTTTT[C/G]TAATAGTTAGGAGTG | 4296 |
rs542501945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604792 | CTGAGAGCAGCTAAG[C/T]GGGTCCTACATTCTG | 4296 |
rs542586416 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609472 | GGCTCATGGCTTTAA[C/G]CCAAATGGGGCCACC | 4296 |
rs542623179 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612371 | CTCTTGGCGATCCAG[A/C]CCTCAAATGTCCATC | 4296 |
rs542822852 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597886 | ACCCCCAGGGCAGGA[A/G]GTCCATGCTCTAAGC | 4296 |
rs543201238 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605608 | CTGGGTTCCAGGATC[A/C/G]GCTCTGTCTTGTCTC | 4296 |
rs543252477 | in-del | -/GTCTGG | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614613 | AGGGGGTGAACCCGA[-/GTCTGG]GTCTGGTCTTGGCTG | 4296 |
rs543314735 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612627 | GCTGCCCATGACGAC[A/G]GGAGGGGAGGACAGA | 4296 |
rs543409399 | snp | A/C/T | 0.000285428 | 0.0119432 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607792 | GCGAAGTCGGGCCTG[A/C/T]GGTGGGGGTCCTGCG | 4296 |
rs543460115 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604466 | AGTGCAGCTGCTGGA[A/G]TAGCAAATGGCGGGG | 4296 |
rs543461937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599040 | TGATTACATGTATGC[C/T]GTGTCGCCCAGGCTG | 4296 |
rs543481196 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615001 | ATATGATATGAGGAC[A/G]AGAAAGCTCTGCCTC | 4296 |
rs543794279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600021 | CCAGCGACCCCAGAC[C/T]CGAAAGATGGATGGG | 4296 |
rs543893204 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608205 | CCCAGCCCTAGATTT[A/G]GGCAGCCACCTCTGC | 4296 |
rs544073308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602475 | ACATGGTGAAACCTC[A/G]TCTCTACTACAAATA | 4296 |
rs544392619 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614382 | CCAGAGGCTCCAGGC[A/G]GGGAGTTCCCGGGTA | 4296 |
rs544452332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609954 | TCCCCGCTGCCCCAC[C/T]GTCCTCAGCCCCCAC | 4296 |
rs544489148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608958 | CAAAACCATTTATGA[A/G]CTAAATAATATTTTT | 4296 |
rs544600174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604857 | GTCCCTAGGTTGGCA[A/C]AGGGACCCACAGGCA | 4296 |
rs544641208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612443 | GGGCTTGCCCAAGCT[C/G]TTGAGCTGTTTCACT | 4296 |
rs544652589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603372 | AAACTGCTTCCGTGA[A/G]GTCTCACAGGGAGGA | 4296 |
rs544676219 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597338 | GACGGAGTCTTGCTC[A/T]GTTGCCCAGGCTGGA | 4296 |
rs544881780 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609991 | TGGCTGCTTGGCTCT[C/G]TTTCTGTGTCCTCCA | 4296 |
rs545246380 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598138 | CCTTCCAGTGTGAAG[C/G]CTTCCTGTGCAGTGT | 4296 |
rs545350564 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613921 | AGTGTTGTCTCCCGG[C/T]CCCCCGCATCTCGGG | 4296 |
rs545461677 | in-del | -/CATCT | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601091 | CATTCATTCAATCAA[-/CATCT]CATCTACTGACCCAT | 4296 |
rs545517734 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606886 | CAGGGGCCCAAGGCC[A/G]GCTCCCAGGCCACAT | 4296 |
rs545654467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606137 | TCCCTCCATCATCAC[A/T]GTCAGGCTTCAGAGA | 4296 |
rs545689223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605702 | GCCTATTGTGGCCTC[A/C]CCAAGGTGCCCACGG | 4296 |
rs545726160 | snp | C/T | 1.67253e-05 | 0.00289178 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613301 | TGTCACACTGATGTC[C/T]TCATCGGGGTCCTGG | 4296 |
rs545792817 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601715 | GAGCCAAAATCACAC[C/G]ACTGCACTCCAGCCT | 4296 |
rs545828088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608807 | TTTTAGTAGAGACAG[C/G]GTTTCTCCATGTTGG | 4296 |
rs545865162 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607942 | ATAAGCTGTGCGAAG[A/G]GCTCGGGGCAGGTGG | 4296 |
rs545874814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599888 | ACTAGCATCTTCCCT[C/G]GTCCCACAGGTCCCA | 4296 |
rs545990752 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615545 | TACTTTGCCGTTACC[C/T]AATGGCTACTCAACT | 4296 |
rs546378902 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615937 | GGTCCGGAGACTAGG[C/G]AGCTGTCGCCTGCAC | 4296 |
rs546609470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601979 | GAGGCCAAGGTGGGC[A/G]GATCACGAGGTCAAG | 4296 |
rs546982222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610454 | GTCCTAAAGCACTTA[C/T]CGTATCTCCGCCCTC | 4296 |
rs547840140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598743 | GTGACCTACTTGACT[C/T]AACTTCCACCGCCCT | 4296 |
rs548013483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600437 | GCCCCAGGGGTTCCA[A/G]GCTCAGAGAGGTTGA | 4296 |
rs548125857 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605403 | CTGGGTCCAGCTTCC[C/T]TTGGGTACCAAATGC | 4296 |
rs548151677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607076 | TCCCACTCCCAGACC[A/G]ACATGCAAATACTTC | 4296 |
rs548360019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601146 | CCAGTCCTGAGACTC[C/T]TCGGCTCTCAACTCT | 4296 |
rs548773585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602000 | CGAGGTCAAGAAATC[G/T]AGACCATCCTGGCCA | 4296 |
rs549028820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610133 | GGCATCTTCCACATT[G/T]GCAACTCCAGGCCAG | 4296 |
rs549279947 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612270 | TTGGGCCATGATGGG[C/T]AGCGTGTCGGGGGCT | 4296 |
rs549623992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604608 | TTCTCTGTTGTAAAA[C/T]GCAGGCCAATACTAC | 4296 |
rs549870229 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614113 | GCCTTCAGGGGCAGC[A/G]CCTCAACTCCGGTTG | 4296 |
rs549942073 | snp | A/G | 2.29888e-05 | 0.00339026 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599568 | GCGTTGGCGTGGGGG[A/G]TGTTGTCGGGGACTC | 4296 |
rs549976878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606403 | ATCCATAAAACTTAA[A/G]TTAACAACAAAAATA | 4296 |
rs550219146 | in-del | -/TCT | 0.00398564 | 0.0444627 | upstream-variant-2KB, cds-indel, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615105 | GATTGCCTAAGGCTC[-/TCT]TCTTCTCCTCACCTG | 4296 |
rs550219522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599302 | GACTGTGGTCTCGGC[C/T]TTGCCTCCTTGCATG | 4296 |
rs550256302 | snp | C/G | 0.00040347 | 0.0141976 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605742 | AGCCAGATCCTGCCG[C/G]GGGAGGAAGGCCACT | 4296 |
rs550353076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605641 | CCTTGGTTTCCTAGT[C/T]TCTAGAATGAGAGCA | 4296 |
rs550574045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601303 | AGACCAACTGGGATG[C/T]CACTTCCTCTGTGAA | 4296 |
rs550646265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607196 | ACCAATCCCAGCGCG[A/G]TGAGCACACAGGCCT | 4296 |
rs550681023 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610463 | CACTTATCGTATCTC[C/T]GCCCTCCTCTCCCTC | 4296 |
rs550810243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610272 | TGGTCTCAAAATCTA[C/T]CCACTCCTCTGAGCC | 4296 |
rs550904972 | snp | A/G | 3.30551e-05 | 0.00406528 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608300 | CTTAGAGAAGGTGGA[A/G]GCCTTGATAACCTCA | 4296 |
rs551169350 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601926 | AAGAAAGAGTTGGCC[A/G]GGTGCGGTGGCTCAC | 4296 |
rs551724190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599119 | CTCACGTGATCCTCC[C/G]AGAGTGCTGGGATCA | 4296 |
rs551863776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612126 | CTACTGCTGCTCTCC[A/C]GCCTGCACTCTGGGC | 4296 |
rs551941259 | snp | A/G | 0.000453412 | 0.0150499 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599576 | GTGGGGGGTGTTGTC[A/G]GGGACTCCCCGCGCT | 4296 |
rs551980326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606481 | AGAAAATTAGTAGTA[C/T]ATAGTGTCATACAAT | 4296 |
rs552024637 | snp | A/G | 9.6446e-05 | 0.00694361 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598616 | GTCCCCGGTGGGGGT[A/G]AGACAGTGCCTCCTG | 4296 |
rs552032985 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615481 | GGGGAGTCCACGCCT[C/T]CACCTTTTCCCCGCC | 4296 |
rs552152634 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614192 | CTGCCTGTTCCTGGC[C/T]CCGTCTCCTTTGGCC | 4296 |
rs552223961 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598800 | TGTAATAGTTAGGAG[G/T]GAGGCCTCTGCAGCA | 4296 |
rs552446631 | snp | C/T | 0.000336952 | 0.0129755 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613678 | GCCGGCCTCCTCCAC[C/T]GCCCCCACCACCCCC | 4296 |
rs553105616 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607484 | CTCGCGCGCCGCTCG[C/T]GTCAGCTCCTCCTCG | 4296 |
rs553107892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599903 | GGTCCCACAGGTCCC[A/G]TGGCCTCCCCATCAC | 4296 |
rs553375941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609734 | TGCCCTGTGTGACAC[C/G]GCTGTCATGGGGGCA | 4296 |
rs553726160 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612302 | GAAATGATGGGAGAT[C/G]GAGTCTCCCTTAGCC | 4296 |
rs553978471 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604731 | AGGCGATGGGCTGGG[A/T]GGGATGGGAGGAGTG | 4296 |
rs554013075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611179 | TGGTCCCTACTTCTC[C/T]TTTCTGGGAGGCCTG | 4296 |
rs554052588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604183 | GTTTCTCTTCATAAA[C/T]AATTAACAAATTCTT | 4296 |
rs554276927 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597826 | TAAGACTCCAACCCT[A/G]GCTGGGGCAGCAGGA | 4296 |
rs554314267 | snp | C/T | 1.75157e-05 | 0.00295932 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605993 | ACTGGGACCCCAAGC[C/T]CAGCATGCTCGCCGC | 4296 |
rs554632378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605565 | GCCTGGGCTGTATGC[C/T]GCTTGATCGTGGGCC | 4296 |
rs554655454 | in-del | -/A | 0.347253 | 0.230308 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602803 | AACAAGACTCCTTCT[-/A]AAAAAAAAAAAAAGA | 4296 |
rs554766853 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598903 | CCTTAAATTTCCTCA[C/T]CTAAAAATGGGCATC | 4296 |
rs554825785 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65616121 | CCGGGCCTTGCACCA[C/T]TGACTGTCCCGGCCG | 4296 |
rs554852996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606577 | CCTAAGGCAGGGAGC[C/T]TGGGGGCGGGGAGGA | 4296 |
rs554945636 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607674 | CTCGTCGAAGAGACC[C/G]TGGATCTCGCGCTTC | 4296 |
rs555446893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601538 | CAGGTGGGATGATCA[C/T]GAGGTCAGGAGATCG | 4296 |
rs555604917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609874 | GCTTAAAGCAACAAG[A/C]CCTGATCCTGCTGCT | 4296 |
rs555777843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603176 | AAATGAGAGTGAACA[C/G]AAGTTCCTGCAGTCA | 4296 |
rs555794723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603938 | TATCCCTGGGGGCTG[C/T]GGCTCTCTCAGTTTG | 4296 |
rs555812807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610562 | ATTTAGCAAGCCCCC[C/G]ACGACAAGCTCATTC | 4296 |
rs556073656 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606528 | AATAAGTAAAATTAA[C/T]GCTGCTTGGGGAGTT | 4296 |
rs556133430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605360 | ACTTGTTTGGCTCCA[C/T]CCCACACAGGCTGAT | 4296 |
rs556372104 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598040 | GCTCTGGTCCTCCCA[A/G]CCAGCTGGGTACAGT | 4296 |
rs556392903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598780 | TCCGTGGTGCCTCTG[C/T]TTTTTGTAATAGTTA | 4296 |
rs556755106 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613819 | CGTGGTCCCCACCCC[C/T]GCTGGCTGCCAAGGC | 4296 |
rs556877193 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602727 | GGAGAATTGCTTGAA[C/T]GTGGGAGGTGGAGGC | 4296 |
rs556976619 | snp | C/G | 4.58831e-05 | 0.00478952 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616306 | GCGGGCAGCAGCGGC[C/G]GGGCCATGGGGTCGC | 4296 |
rs557077431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606601 | GGGAGGAAGAGGGGA[C/T]AGTGAGTGGGCTCCG | 4296 |
rs557115924 | snp | A/C | 4.23155e-05 | 0.00459956 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606102 | GGGGAAACCGATGAA[A/C]TCGGAGATAATCTTT | 4296 |
rs557254674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608675 | CAGGCTGGAGTGCAA[C/T]GGCGTGATCTTGGCT | 4296 |
rs557356559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601584 | ACACGGTGAAACCCT[A/G]TCTCTACTAAAAACA | 4296 |
rs558283010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603429 | GGCAACAAGCTTCAC[A/G]GGGCAGTTGCTATCA | 4296 |
rs558284818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611064 | CTTTAGGGCTCCCTG[G/T]CCTCTGATAGGGACC | 4296 |
rs558308228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612894 | ATGGGCACCCCTGGT[C/T]AGCTGGGACCCCCTA | 4296 |
rs558396220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598925 | ATGGGCATCCAGGAG[C/T]GCTTAGTTCTCTGGT | 4296 |
rs558396227 | snp | A/G | 0.000332154 | 0.0128828 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605872 | TGATGGGAGGGCAAG[A/G]AGGGGTGCTTTAGGA | 4296 |
rs558429457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605507 | GAGGCTTCTTGCAGG[C/T]CAGGTCTGAGCAAGG | 4296 |
rs559076384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607035 | GCCCACTAGACCTTC[C/T]CAGAACTTTCGTGAA | 4296 |
rs559143508 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615398 | GGTCGTGACGTACGA[G/T]GTCCAGCATTAAAGG | 4296 |
rs559237415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606812 | CTTGAAGTCTGGGAT[G/T]TGGGTTGGGGGGAGC | 4296 |
rs559241003 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609617 | AAGGGTCTGAAGGGC[C/T]CCTCTACTTTTCAGG | 4296 |
rs559364255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601718 | CCAAAATCACACCAC[C/T]GCACTCCAGCCTGGG | 4296 |
rs559402140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600967 | TTACCTCACCCAACT[C/G]CCACCCCGGCCACTG | 4296 |
rs559452926 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615590 | GCCCAGTCGTCTACC[A/C]TGGGTTGGCAACGCC | 4296 |
rs559746575 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605684 | CTCCTGCTTTGCCTA[C/T]TAGCCTATTGTGGCC | 4296 |
rs560052023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610050 | TCAGAGCATGACCTC[C/T]CCTCAACCTCTGCCC | 4296 |
rs560087728 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615374 | GTAGACGCCGCTGGG[A/C]GCGAAATCGGTCGTG | 4296 |
rs560208755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610710 | TAGCCACTTGTGGCA[C/T]CCCAGACTGGCAAAG | 4296 |
rs560461435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603467 | TGAGTGCACCCTGCC[A/G]ATGTGCCACTCCTTG | 4296 |
rs560470440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602595 | AGGTTGTAGTGAGCC[A/G]AGATTGCACCACTGC | 4296 |
rs560632256 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598557 | TGATGAGGCCCAGGG[A/G]TGGTGAACGTGGGGT | 4296 |
rs560841756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604948 | TCCTCCCTGCAATGC[C/T]GGAGCCCTGCCTTCT | 4296 |
rs560981301 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614489 | AAAAGCCCCCAGCTG[C/T]GTGCTCTGCTGCCTA | 4296 |
rs561083640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606264 | GGGTGGGGCATCTCA[G/T]CTAGCCCTTGGGCTG | 4296 |
rs561220400 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614091 | CCCCCGCCAAGTGTA[A/G]GGTGGGGCCTTCAGG | 4296 |
rs561470290 | snp | C/T | 3.37838e-05 | 0.00410984 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613469 | AGACACATAGTTGGA[C/T]GGGAAGATGCCCACC | 4296 |
rs561533737 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612571 | CCTTAGCCTTGACTG[A/C]CAAGGAGGGCTTCCC | 4296 |
rs561834235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608170 | AGCCAAGTGGTTTGG[A/G]TCCCTGTCCCTGGAC | 4296 |
rs561998846 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615636 | GCCCAAACGCTTTTA[A/C]GCTCGAACTTGCTTT | 4296 |
rs562181241 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597908 | GCTCTAAGCCCTAGG[G/T]CAGGGGCCGCAGTAG | 4296 |
rs562218156 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600488 | AGCCAGTGAAAGGTG[C/G]AGCCGGCCTCACCCC | 4296 |
rs562233471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601888 | TGAGTTTAAACAGAA[A/G]AGGGGAAATCATGTT | 4296 |
rs562279624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610211 | CCACCTTTACTATCC[C/T]GGCATGCCCAGTAGA | 4296 |
rs562466801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603571 | GCTTATGCCGGGGAC[A/C]ATCTCACAGGGTCTG | 4296 |
rs562625883 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597290 | GTGAGCCACCATGCC[C/T]GGCCTATGGTTTTTT | 4296 |
rs562764624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610991 | GCATGGGAGGTCAGG[G/T]GTCACCCAGAGGAGA | 4296 |
rs563134665 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597653 | CCCAGGAGAGGCATG[A/C]AGTACAAGGCATCCA | 4296 |
rs563263787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599062 | CCCAGGCTGGAGTCC[A/G]GTGTCATGATCACCG | 4296 |
rs563294957 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604531 | GACAGGCAAGAGCAG[A/C]TCAAATCCCTGCTCT | 4296 |
rs563384057 | snp | C/G | 3.74287e-05 | 0.00432584 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599512 | CTTGAGCGAGAAGCA[C/G]ATGAGCGGGGAAGGG | 4296 |
rs563419653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606984 | TAAGGAAAGCTACTC[C/G]TCTGAGTCGGAGATG | 4296 |
rs563457050 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615030 | TCGTAGAGCTAGTTG[A/G]ATGGGGTGGGGAAGA | 4296 |
rs563803526 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608678 | GCTGGAGTGCAATGG[C/T]GTGATCTTGGCTCAC | 4296 |
rs564010005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600933 | GTCAGCCCCAACCCT[C/T]ACTCAGACTCTCTGC | 4296 |
rs564297142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610825 | ACCCAAAGTTTCAGG[A/C]CTTCTTTGTACTTGT | 4296 |
rs564313201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602525 | GTGGCACATGCCTGT[A/G]ATCCCTGCTACTTGG | 4296 |
rs564349949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601914 | ATGTTTAAAAAAAAG[A/G]AAGAGTTGGCCGGGT | 4296 |
rs564386174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609020 | AAATGACTTGGCAGA[A/G]GTCATACAACAAATA | 4296 |
rs564577728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604864 | GGTTGGCACAGGGAC[C/T]CACAGGCAAGGGAGG | 4296 |
rs564618484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604469 | GCAGCTGCTGGAGTA[A/G]CAAATGGCGGGGCAG | 4296 |
rs564656181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611751 | CATTTTTTCTGGAAA[A/G]AAAACGGAGGAAAAA | 4296 |
rs565035628 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598142 | CCAGTGTGAAGGCTT[C/T]CTGTGCAGTGTAGTG | 4296 |
rs565087687 | snp | A/G | 1.67438e-05 | 0.00289338 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613318 | CATCGGGGTCCTGGC[A/G]AGCTGCCTTCACAGC | 4296 |
rs565088087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610023 | CTTCAGCCATTTCGG[C/T]GCTGGTGCTTCTCAG | 4296 |
rs565496001 | snp | A/G | 0.000187406 | 0.00967822 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599659 | GAGCAGGGCGGTGCC[A/G]CGCAGCAGCGCCCGC | 4296 |
rs565589952 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613932 | CCGGCCCCCCGCATC[C/T]CGGGCTTCTGGAGGA | 4296 |
rs565593674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605706 | ATTGTGGCCTCCCCA[A/G]GGTGCCCACGGAAGG | 4296 |
rs565633203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606548 | CTTGGGGAGTTCAGA[C/G]GTAACAGGCTAGACC | 4296 |
rs565672149 | snp | G/T | 4.98815e-05 | 0.00499382 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605878 | GAGGGCAAGGAGGGG[G/T]GCTTTAGGAATTTCA | 4296 |
rs565855091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600314 | AGGAGGAAAATGAGG[C/T]TCAGAGGGGTCAGTA | 4296 |
rs565998898 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614215 | CTTTGGCCCCGACGG[C/T]TCCGACCCCGCTCCC | 4296 |
rs566149484 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615423 | TAAAGGGGGCGGGCC[C/G]AGAGGGGCGTGCTTC | 4296 |
rs566233988 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615945 | GACTAGGGAGCTGTC[C/G]CCTGCACCCCGGGAG | 4296 |
rs566348393 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606858 | GATGAAGTAGAGCCA[C/G]GACCCCAACCTGCAG | 4296 |
rs566384998 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610682 | CAACACTTGCTGCTT[A/C]TTGGCCTGTCTCTAG | 4296 |
rs566440068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609198 | TTGTTGAGGCAGGAG[C/T]GTGAATCAGAACCCC | 4296 |
rs566568798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601421 | TGCTTCATCATATGA[A/G]GTCAGGGCAGTGTTT | 4296 |
rs566592915 | snp | G/T | 0.000347581 | 0.0131784 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608437 | CACTCTCAATGGGCT[G/T]CAGCAGCAAAACTAG | 4296 |
rs566638931 | in-del | -/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615411 | AGGTCCAGCATTAAA[-/G]GGGGGCGGGCCGAGA | 4296 |
rs566832691 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610535 | CTGGCTGCTGGAGGC[A/G]GGGACCTGAGCATTT | 4296 |
rs566860280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603061 | TGAGCCATGATCATG[A/C]CATTGCAGTCCAGCC | 4296 |
rs567043025 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597556 | CGGCCTCGGCCTCCC[A/C]AACTGCTGTGATGAC | 4296 |
rs567048780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603888 | TGGCCTTCTGGCCAC[A/G]CATCTGCAATTTCAT | 4296 |
rs567083853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610898 | AAGCCCCATCCTCTG[C/T]TTTCTCTCCAAGCTC | 4296 |
rs567323181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612786 | TTAACTTGTCCAAAC[C/T]GCAGCTGCAGGCTGG | 4296 |
rs567464398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612354 | TGATTTCAGGCTAGG[C/T]CCTCTTGGCGATCCA | 4296 |
rs567691308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605232 | ACAGAAAGGCCCCGA[A/G]CTATCCTGGATGTGG | 4296 |
rs567748075 | snp | A/G | 0.000160527 | 0.00895754 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605738 | GCTCAGCCAGATCCT[A/G]CCGGGGGAGGAAGGC | 4296 |
rs567758949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598754 | GACTCAACTTCCACC[A/G]CCCTTCCTGCTCCGT | 4296 |
rs567936993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606590 | GCCTGGGGGCGGGGA[A/G]GAAGAGGGGATAGTG | 4296 |
rs568072531 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614459 | CATCACAGCAGGCTT[C/T]TGAGATCTAGAAAGA | 4296 |
rs568343394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600492 | AGTGAAAGGTGGAGC[C/T]GGCCTCACCCCAGGC | 4296 |
rs568442309 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65616203 | GGGGAGGCCATGGCG[G/T]GAGCGTGAGGCCGGG | 4296 |
rs568649756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608610 | AGGTCAGACATTTCT[C/T]TTCTTTTCCTTTTTT | 4296 |
rs569182520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604037 | GCCATGAAATACTTC[A/G]AGGAGATGAGGAAGG | 4296 |
rs569226707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612081 | ATGCTTTTCCAGTGA[C/T]CACACTGAGCCTGGC | 4296 |
rs569473618 | snp | C/T | 0.0013614 | 0.0260547 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598595 | GTGCCAGGAGCAGAG[C/T]GTGATGTCCCCGGTG | 4296 |
rs569602926 | snp | C/T | 0.000424157 | 0.0145567 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613640 | CGGGTTGGCATAACC[C/T]GCTGCCTTTGGAGAC | 4296 |
rs569639877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612825 | ACTTCTGAAGCTGGC[C/G]CAGGAAGACTCTGCT | 4296 |
rs570112119 | snp | A/C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599572 | TGGCGTGGGGGGTGT[A/C/T]GTCGGGGACTCCCCG | 4296 |
rs570257247 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615760 | CTTTTCCGGGTCCCA[A/G]TTGGAATCGTTGGGC | 4296 |
rs570308435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600662 | ATTAAGGACAAGGGA[C/T]TCTAGGATGGGCTCT | 4296 |
rs570418299 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608384 | CTCTCGGGCCAGGCC[A/G]AAGTCGGTGATCTTC | 4296 |
rs570447246 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615729 | TGCGCTTGCGCATTC[A/C]TGCCGTCAAGTTTTC | 4296 |
rs570554901 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607334 | GCGCTTGAATGTCCC[A/G]CGGCGGCGGCGCACG | 4296 |
rs570591428 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615368 | CCGGAAGTAGACGCC[G/T]CTGGGAGCGAAATCG | 4296 |
rs570738119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601315 | ATGTCACTTCCTCTG[A/T]GAAGCCCTCCCAGAA | 4296 |
rs570803239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610364 | AGATGGCTGTCACGA[A/G]CATGAAACAAGACCA | 4296 |
rs570838078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609612 | TCATGAAGGGTCTGA[A/G]GGGCCCCTCTACTTT | 4296 |
rs571025331 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603696 | CGTGGAGTGTGGGAT[G/T]GGGCTAGGGGAACCA | 4296 |
rs571295508 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602160 | GTGAGCCGAGATCCC[A/G]CCACTGCGCTCCAGC | 4296 |
rs571622816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605168 | AGCCCCTCTTCATCA[A/G]TGCTTGGAGGGAATG | 4296 |
rs571623126 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597737 | CCTGGTTACCTCCAA[A/G]AAAGGTGACAGGCTA | 4296 |
rs571678622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612216 | CTCTCTAAATGCTGC[A/G]TGCACCAGGAAACCC | 4296 |
rs571705932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612765 | CACCTGAGAGATACC[A/G]ATTTCTTAACTTGTC | 4296 |
rs571761427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604691 | CTGTTGTTACAACTA[C/T]CAAGTGTAGCTCAGG | 4296 |
rs571773340 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615692 | AGGGCACCCCTCGCG[C/T]CCTACCGCGCCATCA | 4296 |
rs571799375 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611582 | AGGCTCCTTCCTCCC[C/G]CAAGTCCTCCACCCC | 4296 |
rs571988016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598681 | CCCAACTGCTGAGGT[C/T]CCCAAGACACTGTCC | 4296 |
rs572043274 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598985 | AAGCCTTGCAAACAG[A/T]ACTTGGCACAAGTAA | 4296 |
rs572089175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612492 | TGAAATTGAGGCTCC[C/G]AGTTGGAGTAACCAG | 4296 |
rs572336035 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613978 | TGTGGTCAGGCCGGG[A/G]GGGTGGGGCCCCGGG | 4296 |
rs572463673 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602368 | TACAAAAATTAGGCC[A/G]GGCATGGTGGTTCAC | 4296 |
rs572517730 | snp | C/T | 2.09804e-05 | 0.00323879 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607493 | CGCTCGCGTCAGCTC[C/T]TCCTCGCGGCTCAGT | 4296 |
rs572647198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599947 | GGCCTTTCACAAGAT[A/G]GGCACTGGGAGGGGA | 4296 |
rs572661414 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603153 | GAGAAGATAGGGTCC[A/G]GCAGACAAAATGAGA | 4296 |
rs572747807 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614869 | TTTTAGTGGAGACGG[G/T]TTTCACCATGTTGGC | 4296 |
rs572875290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602384 | GGCATGGTGGTTCAC[A/G]CTTGTAATCCCAGCA | 4296 |
rs572912038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601742 | GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA | 4296 |
rs573026581 | snp | A/G/T | 0.010546 | 0.0718478 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599724 | GCTCTGCGGGGACAG[A/G/T]CCTCTTGGGCTCCTC | 4296 |
rs573336311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608891 | AAAGTGCTGGGATTA[C/T]AGGCCACTGCACCTG | 4296 |
rs573679820 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609411 | TTCTTGGCCACAAAG[G/T]AGGAGCTTGGGGTAA | 4296 |
rs573751796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604741 | CTGGGTGGGATGGGA[A/G]GAGTGAGTTTAAACG | 4296 |
rs573765683 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612171 | GCTCCTGGTCCCTGC[C/T]GTGTGCTGGGTCCTG | 4296 |
rs573898636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611574 | GCAGTTCCAGGCTCC[A/T]TCCTCCCGCAAGTCC | 4296 |
rs574349499 | snp | C/T | 3.67667e-05 | 0.00428743 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599494 | GGGCGGGGAGTCGGG[C/T]GTCTTGAGCGAGAAG | 4296 |
rs574384864 | snp | A/G | 7.18783e-05 | 0.00599456 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606034 | TTGAGTCCTCCAGAC[A/G]TCGGGGGGACTGGCG | 4296 |
rs574475653 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605573 | TGTATGCCGCTTGAT[C/T]GTGGGCCTGTAGGTC | 4296 |
rs574494544 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614903 | GCTGGTCTCAAACCC[C/G]TGACCTCGTGATCCT | 4296 |
rs574632349 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613816 | GCCCGTGGTCCCCAC[A/C]CCCGCTGGCTGCCAA | 4296 |
rs574705603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606952 | CCTCACTGCTTTCTT[A/G]AGCCCCTGGGTCTGG | 4296 |
rs574886289 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601556 | GGTCAGGAGATCGAG[A/T]CCATCCTGGCTAACA | 4296 |
rs575103977 | snp | C/T | 8.33215e-05 | 0.00645398 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607754 | CCTGTGCCTCCAGCG[C/T]CTCCAACTGCTGCAG | 4296 |
rs575601044 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612420 | CTGTGGGTTGGGGAT[C/G]GCAGGTCGGGCTTGC | 4296 |
rs575637761 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611640 | GGGCTAGGGAGGGAG[C/G]AGGGGCTGGAGCAGG | 4296 |
rs575920747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605413 | CTTCCCTTGGGTACC[A/T]AATGCCAGGTGGGCT | 4296 |
rs575946415 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606349 | TTCTGGCTCTTCCAC[-/TTA]TTAACTGTGTAACAA | 4296 |
rs575958819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604345 | ACAGGCTCTCAAGTT[A/C]TCCTTTGGCCCATCT | 4296 |
rs576248733 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598060 | CTGGGTACAGTGTTG[G/T]GCCCCAGTAGGGCAG | 4296 |
rs576289239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604833 | GCAGGTGTGGGGGCT[C/G]TGAGGATGGTCCCTA | 4296 |
rs576676136 | snp | A/G | 0.000149278 | 0.00863808 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606105 | GAAACCGATGAAATC[A/G]GAGATAATCTTTATT | 4296 |
rs576678190 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614584 | CAAAACGGGGTTACA[C/G]AACCACACTTGGGAA | 4296 |
rs576778350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600383 | TTGTGCCAGGCCTGA[A/G]CTGAATGGCATAGGG | 4296 |
rs576793727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608679 | CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCACT | 4296 |
rs576835186 | snp | C/T | 0.000136745 | 0.00826764 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607904 | TCTGTACCTCACCTG[C/T]CCTCCCCGTCCTCTT | 4296 |
rs577044473 | snp | A/G | 3.36513e-05 | 0.00410177 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606662 | GGAGCTGGGGGGCGG[A/G]GAGGGGCATGAGAGG | 4296 |
rs577738080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611076 | CTGGCCTCTGATAGG[A/G]ACCTGGCCACCAGCT | 4296 |
rs577882112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603447 | GCAGTTGCTATCAGC[A/G]TAGCTGAGTGCACCC | 4296 |
rs577921163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610669 | CCCCTTTGAAGACCA[A/G]CACTTGCTGCTTCTT | 4296 |
rs578019935 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604434 | AGTTCAGTCCCTGCA[A/G]GACAGATGCTGGGGG | 4296 |
rs578101720 | snp | C/G/T | 1.85751e-05 | 0.00304749 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605715 | TCCCCAAGGTGCCCA[C/G/T]GGAAGGAGCTCAGCC | 4296 |
rs745368729 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609741 | TGTGACACGGCTGTC[A/C]TGGGGGCAGCATAGG | 4296 |
rs745424431 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603993 | CATTTCAGATTTCTA[C/T]GGGCACAGATGTCTA | 4296 |
rs745473329 | snp | A/G | 0.00028397 | 0.0119124 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606090 | GGCTCCACTGCAGGG[A/G]AAACCGATGAAATCG | 4296 |
rs745592257 | snp | C/G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603511 | AGGGACCAGAACAGC[C/G/T]CACTGGGGACAGGGT | 4296 |
rs745651508 | snp | C/T | 3.40177e-05 | 0.00412404 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607874 | CGTGGGTGGATGTGT[C/T]CTGGGCCAGGGAGCT | 4296 |
rs745680257 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598924 | AATGGGCATCCAGGA[A/G]CGCTTAGTTCTCTGG | 4296 |
rs745719453 | in-del | -/AAA | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602203 | GTGAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 4296 |
rs745917799 | snp | G/T | 5.74542e-05 | 0.00535946 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607321 | CCCGGAGCTTGCTGC[G/T]CTTGAATGTCCCGCG | 4296 |
rs745958741 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604989 | CTGGCTTCCTAAGCA[C/G]TCTATACGTGAGAAG | 4296 |
rs746007884 | snp | C/T | 6.15593e-05 | 0.0055476 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607475 | TGACCGCTGCTCGCG[C/T]GCCGCTCGCGTCAGC | 4296 |
rs746033134 | snp | G/T | 5.27644e-05 | 0.00513609 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613235 | GAGGGCAATGATGTT[G/T]GGGTGTGCCAGCATG | 4296 |
rs746165183 | in-del | -/GGGAAGGGGGCGGCTCGGTCGGGC | 0.000472398 | 0.0153615 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599519 | AGAAGCAGATGAGCG[-/GGGAAGGGGGCGGCTCGGTCGGGC]GGGAAGGGGGCGGCT | 4296 |
rs746194211 | snp | A/G | 4.16884e-05 | 0.00456535 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598360 | TGCCCTGCAGTCCTG[A/G]GGGCCCCCCTGGAAG | 4296 |
rs746209250 | snp | G/T | 1.83202e-05 | 0.00302651 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605721 | AGGTGCCCACGGAAG[G/T]AGCTCAGCCAGATCC | 4296 |
rs746218365 | snp | A/G | 9.42108e-05 | 0.00686269 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616280 | CCCATGAGGGTCCCG[A/G]GAGGGGGGGCGCGGG | 4296 |
rs746230771 | snp | C/T | 0.000118061 | 0.00768222 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613625 | CAGGGCTGTCCACAC[C/T]GGGTTGGCATAACCC | 4296 |
rs746232637 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608344 | CGTAGGTGCCCGCGG[C/G]ACTCATTTGTGTGGT | 4296 |
rs746257533 | in-del | -/G | 1.88752e-05 | 0.00307201 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607540 | CAGCGATGGTGGAGA[-/G]GGTCAGCCTGGCACC | 4296 |
rs746307972 | snp | A/G | 1.75477e-05 | 0.00296202 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598443 | AGGGTGCTCGGCGGG[A/G]TGCAGGCTGTGGTGA | 4296 |
rs746313672 | snp | A/T | 2.7924e-05 | 0.00373647 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599765 | CTAGGCCGCGGGGGG[A/T]TACCTGCGGGCAGAG | 4296 |
rs746476599 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608341 | AGGCGTAGGTGCCCG[C/T]GGCACTCATTTGTGT | 4296 |
rs746479379 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600270 | ACATGGCAGCCCTGA[A/G]GGCATAAATCCCTGT | 4296 |
rs746497837 | snp | A/G | 1.78109e-05 | 0.00298414 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606023 | CTCTCCATTGCTTGA[A/G]TCCTCCAGACGTCGG | 4296 |
rs746555616 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602074 | AGGGCATGGTGGCAC[A/G]CACCTGTAGTCTCAG | 4296 |
rs746566431 | snp | A/G | 1.9608e-05 | 0.00313108 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606084 | TCTGCAGGCTCCACT[A/G]CAGGGGAAACCGATG | 4296 |
rs746607052 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615628 | ACGCATGCGCCCAAA[C/T]GCTTTTACGCTCGAA | 4296 |
rs746618739 | snp | C/T | 2.3957e-05 | 0.00346091 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598342 | ACCCATGTCTTTGGT[C/T]TGTGCCCTGCAGTCC | 4296 |
rs746621167 | snp | C/T | 0.000101025 | 0.00710651 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616276 | CGCCCCCATGAGGGT[C/T]CCGGGAGGGGGGGCG | 4296 |
rs746795095 | snp | C/G/T | 0.000187546 | 0.00968215 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613439 | CACCTCGCAGGGGGG[C/G/T]GGGCCGCCACCCCGA | 4296 |
rs746813047 | snp | A/C | 1.66774e-05 | 0.00288763 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607759 | GCCTCCAGCGCCTCC[A/C]ACTGCTGCAGGATGG | 4296 |
rs746845515 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609615 | TGAAGGGTCTGAAGG[A/G]CCCCTCTACTTTTCA | 4296 |
rs746858638 | snp | C/T | 1.6631e-05 | 0.00288362 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608275 | GGCCGCACCTCCAGA[C/T]GTCACTGCCCTTAGA | 4296 |
rs746877428 | snp | A/G | 1.87605e-05 | 0.00306266 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599515 | GAGCGAGAAGCAGAT[A/G]AGCGGGGAAGGGGGC | 4296 |
rs746967352 | snp | C/T | 6.49498e-05 | 0.00569831 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599554 | CGGGCAGGGCGCGGG[C/T]GTTGGCGTGGGGGGT | 4296 |
rs747051146 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604053 | AGGAGATGAGGAAGG[C/T]TGCTATCTCTCAGAA | 4296 |
rs747090171 | snp | C/T | 1.78835e-05 | 0.00299022 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613194 | ATCACCAGGCACAGG[C/T]TGGGCTCCTCCAGGC | 4296 |
rs747242784 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598753 | TGACTCAACTTCCAC[C/T]GCCCTTCCTGCTCCG | 4296 |
rs747325171 | in-del | -/CTT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610657 | AGGGCCCACCTTCCC[-/CTT]TGAAGACCAACACTT | 4296 |
rs747385158 | snp | A/G | 2.34524e-05 | 0.00342428 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613733 | TAGAGGGCTCTTGAG[A/G]AAGAGGCTCTTCAAG | 4296 |
rs747415433 | snp | A/C | 0.00243486 | 0.0348067 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607225 | CTGGCTCCACCCCCA[A/C]CCCCGCAGCCAATGG | 4296 |
rs747468206 | snp | C/T | 0.000159706 | 0.00893463 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607307 | GCCGCCGTCGCGCGC[C/T]CGGAGCTTGCTGCGC | 4296 |
rs747477088 | snp | C/T | 0.000234171 | 0.0108181 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599758 | CTCCAGGCTAGGCCG[C/T]GGGGGGTTACCTGCG | 4296 |
rs747548622 | in-del | -/CC | 3.22857e-05 | 0.00401768 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599349 | CTCCCTCCCTGGGAA[-/CC]CCCGTCTCCCATATG | 4296 |
rs747598736 | snp | C/T | 2.08888e-05 | 0.00323171 | stop-gained, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613710 | CTGCCACTGCCATTC[C/T]ATGACCCTAGAGGGC | 4296 |
rs747650518 | snp | A/G | 3.30573e-05 | 0.00406541 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607997 | TAACAGCTACGCCAT[A/G]GGCCACAGCAAGGCA | 4296 |
rs747668512 | snp | C/T | 8.51854e-05 | 0.00652575 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608233 | TGCCCTCTGCAGCCC[C/T]GTAGCAGCCCGTCCA | 4296 |
rs747721707 | snp | A/G | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599690 | TGGATCAGCTTGGGC[A/G]TCCCAGAGCTGCTAC | 4296 |
rs747732702 | snp | C/T | 0.00018457 | 0.00960473 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599660 | AGCAGGGCGGTGCCG[C/T]GCAGCAGCGCCCGCT | 4296 |
rs747738670 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612274 | GCCATGATGGGCAGC[A/G]TGTCGGGGGCTTGAA | 4296 |
rs747830130 | snp | A/G | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598521 | CAATGCGGCTGCGAA[A/G]GGGCGAGGGCCGAGG | 4296 |
rs747953183 | snp | A/C | 3.60614e-05 | 0.0042461 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599464 | ACCCAGGTCCAGCAA[A/C]AGGGGTGCAGGAGTG | 4296 |
rs747954057 | snp | A/C | 3.34963e-05 | 0.00409232 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613324 | GGTCCTGGCGAGCTG[A/C]CTTCACAGCCACCAG | 4296 |
rs748057055 | snp | C/T | 1.76474e-05 | 0.00297042 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606006 | GCCCAGCATGCTCGC[C/T]GCTCTCCATTGCTTG | 4296 |
rs748169286 | in-del | -/G | 1.7067e-05 | 0.00292117 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613433 | GCTGGCCACCTCGCA[-/G]GGGGGCGGGCCGCCA | 4296 |
rs748237554 | snp | A/G | 1.66106e-05 | 0.00288184 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605798 | AGGAGATCCTAAGGG[A/G]GATGAGTCATCTGAA | 4296 |
rs748274081 | snp | A/C | 1.68125e-05 | 0.00289931 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608474 | GGGGCCAGATTGTGG[A/C]TGCTCCAGGATCAGG | 4296 |
rs748319680 | snp | A/G | 1.69152e-05 | 0.00290814 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607841 | CGGCGTGCAGCGGGG[A/G]CAGAATAAGAAGGGG | 4296 |
rs748440702 | snp | A/G | 1.74592e-05 | 0.00295454 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606837 | GGGAGCAGGGTTCAG[A/G]TTTGTGATGAAGTAG | 4296 |
rs748489992 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603667 | GTCATGTACTTTCAT[G/T]GACCCAGATGATGCG | 4296 |
rs748491050 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604342 | TTGACAGGCTCTCAA[A/G]TTCTCCTTTGGCCCA | 4296 |
rs748525458 | snp | C/T | 5.38662e-05 | 0.00518943 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613173 | GGCCCACCGGCTGCA[C/T]ACTCCATCACCAGGC | 4296 |
rs748545222 | snp | A/G | 9.40218e-05 | 0.0068558 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599354 | TCCCTGGGAACCCCC[A/G]TCTCCCATATGTGAA | 4296 |
rs748565430 | snp | C/T | 1.81701e-05 | 0.00301409 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613074 | GCCTCGCAGTGCAGG[C/T]AGTGCATCCCACGGG | 4296 |
rs748613462 | snp | C/T | 0.000168905 | 0.00918824 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607294 | TGCTGATACGCTCGC[C/T]GCCGTCGCGCGCCCG | 4296 |
rs748629621 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602503 | ATACAAACATTAGCC[A/G]GGCATTGTGGCACAT | 4296 |
rs748714920 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612136 | TCTCCAGCCTGCACT[C/G]TGGGCTCTAGGAGGC | 4296 |
rs748790856 | snp | A/C/T | 8.41172e-05 | 0.00648481 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613557 | GACAGCACCTCCACA[A/C/T]GGTCACCCTTCCTCA | 4296 |
rs748893878 | snp | A/G | 1.70203e-05 | 0.00291716 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606821 | TGGGATTTGGGTTGG[A/G]GGGAGCAGGGTTCAG | 4296 |
rs748895865 | snp | A/G | 6.76186e-05 | 0.00581418 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599564 | GCGGGCGTTGGCGTG[A/G]GGGGTGTTGTCGGGG | 4296 |
rs749071112 | snp | C/T | 1.70502e-05 | 0.00291972 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608225 | GCCACCTCTGCCCTC[C/T]GCAGCCCCGTAGCAG | 4296 |
rs749202106 | snp | C/T | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607978 | ATGGGCAGTGTGAGC[C/T]TGTTAACAGCTACGC | 4296 |
rs749294156 | snp | A/G | 0.000193867 | 0.00984358 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599639 | CGGCCAAGGCCCAGC[A/G]AGGCGAGCAGGGCGG | 4296 |
rs749367172 | snp | C/T | 3.33034e-05 | 0.00408051 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607745 | CCCGTAGGACCTGTG[C/T]CTCCAGCGCCTCCAA | 4296 |
rs749418467 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611032 | GACCCCGAAACTGGG[A/G]GAAGCTCTCAGTGCC | 4296 |
rs749434963 | snp | G/T | 1.99162e-05 | 0.00315558 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607502 | CAGCTCCTCCTCGCG[G/T]CTCAGTAGTTCCTGC | 4296 |
rs749472889 | snp | A/G | 5.11662e-05 | 0.00505771 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613430 | GAAGCTGGCCACCTC[A/G]CAGGGGGGCGGGCCG | 4296 |
rs749524493 | in-del | -/C | 3.37866e-05 | 0.00411001 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608250 | TAGCAGCCCGTCCAG[-/C]CCCACCAAGGGCCGC | 4296 |
rs749550268 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598257 | TGTGACTCCTCCTAA[C/G]GCAGCTGGAGCTCGG | 4296 |
rs749584621 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602375 | ATTAGGCCGGGCATG[A/G]TGGTTCACGCTTGTA | 4296 |
rs749638210 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615835 | CCTCCTCCTTAGGCC[A/G]GCACCAGCAGAAGCC | 4296 |
rs749661072 | snp | A/C | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606702 | TTACACTGGATGGCT[A/C]GGAACCGGGGAAAGG | 4296 |
rs749671008 | snp | A/G | 1.81678e-05 | 0.00301389 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613050 | TCACGGTGGATGACG[A/G]GCACCAGGGCCTCGC | 4296 |
rs749690694 | snp | A/G | 1.66804e-05 | 0.00288789 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605784 | GCTGGGGGTGTGGAA[A/G]GAGATCCTAAGGGGG | 4296 |
rs749738397 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613858 | CGGAACCTGGGCATC[C/T]GGGCCCTGGCCCTCA | 4296 |
rs749745269 | snp | C/T | 1.72302e-05 | 0.0029351 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598459 | TGCAGGCTGTGGTGA[C/T]GGCAGGGGAGAAGGC | 4296 |
rs749783705 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600462 | GGTTGAGGGCTTGTG[C/T]GGAGCTGTACAGCCA | 4296 |
rs749887466 | in-del | -/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606157 | GCTTCAGAGATAAAC[-/T]TTTAGAGTATGGGGA | 4296 |
rs749916030 | snp | C/T | 3.63227e-05 | 0.00426146 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613024 | GAAACTCACTGTTGT[C/T]GGACTTGAGATCACG | 4296 |
rs750004196 | snp | C/T | 1.80416e-05 | 0.00300341 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613136 | GGGAGGCACGCGCCG[C/T]CCGGCCAGAGCTCGG | 4296 |
rs750035582 | snp | A/G | 2.20753e-05 | 0.00332222 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598539 | GCGAGGGCCGAGGTC[A/G]GCTGATGAGGCCCAG | 4296 |
rs750037514 | snp | C/T | 1.65847e-05 | 0.0028796 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605852 | CATGCGGGACCTTCT[C/T]CTGGTGATGGGAGGG | 4296 |
rs750131457 | snp | A/G | 0.000163867 | 0.00905024 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598631 | GAGACAGTGCCTCCT[A/G]TGAGGATATAGGAGG | 4296 |
rs750219478 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612655 | AGAGCACCAACTCCA[C/T]GAACATGAATTTAGG | 4296 |
rs750244012 | in-del | -/A | 1.84875e-05 | 0.0030403 | frameshift-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606054 | GGGACTGGCGGCCCC[-/A]ATGCCTGGCCTGGCT | 4296 |
rs750269167 | snp | A/G | 0.000138879 | 0.00833189 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599716 | GCTACCGCGCTCTGC[A/G]GGGACAGGCCTCTTG | 4296 |
rs750272895 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612006 | CAAGCCCCTTGTCCA[C/T]GGTCAGCCCAGGCCA | 4296 |
rs750295922 | snp | C/G | 3.87747e-05 | 0.00440294 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613683 | CCTCCTCCACCGCCC[C/G]CACCACCCCCGCTGC | 4296 |
rs750306858 | snp | A/C | 1.95961e-05 | 0.00313012 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607258 | GGGGACGCCCCGGGG[A/C]CCGGCCCTCACCGAG | 4296 |
rs750345450 | snp | A/G | 7.43246e-05 | 0.00609563 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599642 | CCAAGGCCCAGCGAG[A/G]CGAGCAGGGCGGTGC | 4296 |
rs750477481 | snp | C/T | 1.70388e-05 | 0.00291875 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613428 | TGGAAGCTGGCCACC[C/T]CGCAGGGGGGCGGGC | 4296 |
rs750542439 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601483 | ATCCCTGGGCCAGGC[A/G]CGGTGGCTCACATCT | 4296 |
rs750589238 | snp | A/G | 1.83508e-05 | 0.00302904 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606049 | GTCGGGGGGACTGGC[A/G]GCCCCATGCCTGGCC | 4296 |
rs750616138 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608411 | CTTCAGGGTCTTGTG[C/T]TCCATGTCGTCACTC | 4296 |
rs750644193 | snp | C/T | 2.4228e-05 | 0.00348044 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606130 | TTTATTCTCCCTCCA[C/T]CATCACAGTCAGGCT | 4296 |
rs750770665 | snp | A/G | 6.75459e-05 | 0.00581106 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607823 | CCCAGCAGTCTAGGG[A/G]CACGGCGTGCAGCGG | 4296 |
rs750803301 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608976 | AAATAATATTTTTCA[C/T]GTTTCACAGATGAGG | 4296 |
rs750850744 | snp | A/G | 1.66026e-05 | 0.00288115 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607710 | TTCCTGCATGGAATG[A/G]AAGGAGTCCCGCGGC | 4296 |
rs750897139 | snp | A/G | 3.38181e-05 | 0.00411192 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613503 | CCACCCACCTGGCCC[A/G]CCCACCAGCCCTCGT | 4296 |
rs751118360 | snp | A/G | 5.852e-05 | 0.00540894 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598526 | CGGCTGCGAAGGGGC[A/G]AGGGCCGAGGTCGGC | 4296 |
rs751200051 | snp | C/T | 2.77766e-05 | 0.0037266 | synonymous-codon, upstream-variant-2KB | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616335 | GCAGGTGTTGCAGAT[C/T]CTGCGCCAGGGGGTG | 4296 |
rs751204773 | snp | C/T | 1.78557e-05 | 0.0029879 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598436 | AAGGTCCAGGGTGCT[C/T]GGCGGGGTGCAGGCT | 4296 |
rs751259676 | snp | A/G | 1.68074e-05 | 0.00289887 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605769 | CACTCACCATTGAGT[A/G]CTGGGGGTGTGGAAG | 4296 |
rs751284429 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610558 | GAGCATTTAGCAAGC[C/T]CCCGACGACAAGCTC | 4296 |
rs751390937 | snp | A/C | 1.81721e-05 | 0.00301425 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613004 | CACCCCCAACCATGC[A/C]CCCAGAAACTCACTG | 4296 |
rs751406126 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605388 | GATTCCTTCCCCCAT[C/T]TGGGTCCAGCTTCCC | 4296 |
rs751442598 | snp | C/T | 0.00010507 | 0.00724733 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599586 | TTGTCGGGGACTCCC[C/T]GCGCTCGCGTCCTGG | 4296 |
rs751480612 | snp | C/G | 1.66571e-05 | 0.00288587 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606808 | GGTGCTTGAAGTCTG[C/G]GATTTGGGTTGGGGG | 4296 |
rs751664849 | snp | C/T | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599482 | GGGTGCAGGAGTGGG[C/T]GGGGAGTCGGGCGTC | 4296 |
rs751685701 | snp | A/G | 3.08485e-05 | 0.00392725 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613768 | CCATGGCCGGGAGCC[A/G]GCGCTGGGATGTGTG | 4296 |
rs751742517 | snp | A/G | 1.65726e-05 | 0.00287855 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608113 | CCCTTTTCTCTCCCA[A/G]CCCCCACCCCCTTAC | 4296 |
rs751789271 | snp | C/T | 0.000234274 | 0.0108205 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598282 | GCTCGGGGGAGTGGC[C/T]TGGCCCACTCAAGGC | 4296 |
rs751805434 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605991 | GAACTGGGACCCCAA[A/G]CCCAGCATGCTCGCC | 4296 |
rs751866973 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611834 | GGGGCAGGTAGCGGG[G/T]GTCCCTAGATAGTTA | 4296 |
rs751937250 | snp | C/T | 1.69743e-05 | 0.00291322 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613404 | ATCACCTCCTCCAGC[C/T]GCAGCTCCTGGAAGC | 4296 |
rs751951529 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606479 | TTAGAAAATTAGTAG[C/T]ACATAGTGTCATACA | 4296 |
rs752003340 | snp | A/G/T | 5.51033e-05 | 0.00524873 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599495 | GGCGGGGAGTCGGGC[A/G/T]TCTTGAGCGAGAAGC | 4296 |
rs752006388 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605574 | GTATGCCGCTTGATC[A/G]TGGGCCTGTAGGTCA | 4296 |
rs752024811 | snp | C/T | 0.000286801 | 0.0119716 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607661 | CCTTGGCTCGCAGCT[C/T]GTCGAAGAGACCCTG | 4296 |
rs752059855 | snp | C/T | 6.69456e-05 | 0.00578518 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613313 | GTCCTCATCGGGGTC[C/T]TGGCGAGCTGCCTTC | 4296 |
rs752089771 | snp | A/G | 3.97259e-05 | 0.00445661 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599536 | GGAAGGGGGCGGCTC[A/G]GTCGGGCAGGGCGCG | 4296 |
rs752091053 | in-del | -/GA | 7.1182e-05 | 0.00596539 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606845 | GTTCAGGTTTGTGAT[-/GA]GAAGTAGAGCCAGGA | 4296 |
rs752175457 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615443 | GGGCGTGCTTCGGTA[A/G]TGCAGAACTCTCGCT | 4296 |
rs752232114 | snp | A/C | 1.78337e-05 | 0.00298606 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607403 | CAGCTCGCGCTCGAA[A/C]ACCTCTAGCTCCCAC | 4296 |
rs752259089 | snp | C/T | 9.78665e-05 | 0.00699455 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613804 | CCTTCTCTGGGTGCC[C/T]GTGGTCCCCACCCCC | 4296 |
rs752278003 | in-del | -/AC | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610588 | CATTCCAAAGGGGAA[-/AC]ACAGCAGGCTGGGGC | 4296 |
rs752339492 | snp | C/G | 1.6981e-05 | 0.00291379 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613394 | TCCAATGCCGATCAC[C/G]TCCTCCAGCCGCAGC | 4296 |
rs752424509 | snp | A/G | 1.76452e-05 | 0.00297024 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607617 | GACACTCGTTCCAAC[A/G]CTGGGTCCCTTGATT | 4296 |
rs752507549 | snp | C/T | 3.30136e-05 | 0.00406273 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608419 | TCTTGTGCTCCATGT[C/T]GTCACTCTCAATGGG | 4296 |
rs752526164 | snp | C/T | 4.21896e-05 | 0.00459272 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616310 | GCAGCAGCGGCGGGG[C/T]CATGGGGTCGCAGGT | 4296 |
rs752617357 | snp | A/G | 1.81059e-05 | 0.00300876 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598423 | TGAGTCCGGGAACAA[A/G]GTCCAGGGTGCTCGG | 4296 |
rs752634263 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608336 | CATCCAGGCGTAGGT[A/G]CCCGCGGCACTCATT | 4296 |
rs752639569 | snp | C/T | 1.77442e-05 | 0.00297855 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598511 | CTCCAGGGATCAATG[C/T]GGCTGCGAAGGGGCG | 4296 |
rs752687885 | snp | C/T | 1.81543e-05 | 0.00301277 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613672 | CCTCAGGCCGGCCTC[C/T]TCCACCGCCCCCACC | 4296 |
rs752747192 | in-del | -/AA | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602204 | TGAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 4296 |
rs752756299 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598215 | GGCAGCTGCAGAGGC[A/T]GACCCAGCTCCTGTT | 4296 |
rs752831657 | snp | G/T | 1.65405e-05 | 0.00287576 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608093 | CGAGACAACAGGTCT[G/T]TGTTCCCTTTTCTCT | 4296 |
rs752842219 | snp | G/T | 1.6625e-05 | 0.00288309 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605877 | GGAGGGCAAGGAGGG[G/T]TGCTTTAGGAATTTC | 4296 |
rs752914916 | snp | A/G | 3.36378e-05 | 0.00410094 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613612 | GCTCGTAGTCGAACA[A/G]GGCTGTCCACACCGG | 4296 |
rs752958965 | snp | C/T | 0.000139092 | 0.00833826 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599624 | GGCGGCTGCAGGTCG[C/T]GGCCAAGGCCCAGCG | 4296 |
rs753055866 | snp | C/T | 3.6549e-05 | 0.00427471 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599489 | GGAGTGGGCGGGGAG[C/T]CGGGCGTCTTGAGCG | 4296 |
rs753080487 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604620 | AAATGCAGGCCAATA[C/G]TACTACTCCCCTCAC | 4296 |
rs753146804 | snp | C/G | 1.71755e-05 | 0.00293044 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605968 | TCTGGGCTTCCCCAG[C/G]CTTGGGGGAACTGGG | 4296 |
rs753282799 | snp | C/T | 1.85177e-05 | 0.00304278 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599423 | TCACGTCGGGGGCTC[C/T]TGGCTGACCGCTGGC | 4296 |
rs753316830 | snp | C/T | 1.91024e-05 | 0.00309044 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607266 | CCCGGGGCCCGGCCC[C/T]CACCGAGTGGCATGC | 4296 |
rs753358832 | snp | A/G | 5.02197e-05 | 0.00501072 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613283 | CTGGCGAACGCTCTC[A/G]GCTGTCACACTGATG | 4296 |
rs753384688 | snp | C/G | 3.6075e-05 | 0.00424691 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613140 | GGCACGCGCCGCCCG[C/G]CCAGAGCTCGGCTGA | 4296 |
rs753404750 | snp | C/T | 0.000227092 | 0.0106534 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607379 | GTCCACCTGCTGCAG[C/T]AGCAGCGTCAGCTCG | 4296 |
rs753410831 | snp | A/G | 0.000162285 | 0.00900645 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599650 | CAGCGAGGCGAGCAG[A/G]GCGGTGCCGCGCAGC | 4296 |
rs753497181 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605469 | CCTGCTAAAGGCACA[C/G]GGGCTGCCATGGGGC | 4296 |
rs753505783 | in-del | -/A | 3.36349e-05 | 0.00410077 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606664 | AGCTGGGGGGCGGAG[-/A]GGGGCATGAGAGGTG | 4296 |
rs753529001 | snp | A/G | 1.8764e-05 | 0.00306295 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599415 | GCTCCTCCTCACGTC[A/G]GGGGCTCTTGGCTGA | 4296 |
rs753634967 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601561 | GGAGATCGAGACCAT[A/C]CTGGCTAACACGGTG | 4296 |
rs753716966 | snp | C/G | 3.99401e-05 | 0.00446861 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599726 | TCTGCGGGGACAGGC[C/G]TCTTGGGCTCCTCGG | 4296 |
rs753749962 | snp | A/G | 4.94059e-05 | 0.00496996 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598307 | CAAGGCCCCGCTTCC[A/G]GCACCCACGGGGCCT | 4296 |
rs753756607 | snp | A/T | 1.6504e-05 | 0.00287258 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608318 | CTTGATAACCTCAGG[A/T]GCCATCCAGGCGTAG | 4296 |
rs753790026 | snp | A/C | 1.96798e-05 | 0.0031368 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613690 | CACCGCCCCCACCAC[A/C]CCCGCTGCCACTGCC | 4296 |
rs753834812 | snp | C/T | 0.000193274 | 0.00982851 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599715 | TGCTACCGCGCTCTG[C/T]GGGGACAGGCCTCTT | 4296 |
rs753890416 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609388 | GGTGGGGTCCAAGAA[A/G]GTGATGGTTCTTGGC | 4296 |
rs753934548 | snp | C/G | 1.69135e-05 | 0.002908 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607835 | GGGGCACGGCGTGCA[C/G]CGGGGACAGAATAAG | 4296 |
rs753987214 | snp | C/G | 1.67992e-05 | 0.00289816 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613606 | CACTGGGCTCGTAGT[C/G]GAACAGGGCTGTCCA | 4296 |
rs754026041 | in-del | -/AC | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601344 | AATCTCCCTGAACCT[-/AC]ACAGTTATTGCTCAC | 4296 |
rs754035122 | snp | C/T | 0.000214436 | 0.0103524 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599550 | CGGTCGGGCAGGGCG[C/T]GGGCGTTGGCGTGGG | 4296 |
rs754046278 | snp | A/C | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606763 | CGTTTCTCCTCCGGT[A/C]AAGGCCGGGTGAGGC | 4296 |
rs754293695 | snp | C/G | 2.09172e-05 | 0.00323391 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598654 | ATAGGAGGGGCACAG[C/G]GTCAAGCAACCCCCA | 4296 |
rs754390955 | snp | G/T | 1.66034e-05 | 0.00288122 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605867 | CCTGGTGATGGGAGG[G/T]CAAGGAGGGGTGCTT | 4296 |
rs754406857 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610146 | TTTGCAACTCCAGGC[C/G]AGACAAATTGGTTCA | 4296 |
rs754442423 | snp | C/T | 3.73134e-05 | 0.00431918 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607382 | CACCTGCTGCAGCAG[C/T]AGCGTCAGCTCGCGC | 4296 |
rs754471887 | snp | C/T | 8.75388e-05 | 0.00661527 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599655 | AGGCGAGCAGGGCGG[C/T]GCCGCGCAGCAGCGC | 4296 |
rs754485269 | in-del | -/G | 5.07357e-05 | 0.00503639 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606818 | TCTGGGATTTGGGTT[-/G]GGGGGGAGCAGGGTT | 4296 |
rs754488458 | snp | A/G | 0.000112894 | 0.00751229 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599732 | GGGACAGGCCTCTTG[A/G]GCTCCTCGGGCTCCA | 4296 |
rs754535717 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612073 | AATGTCTCATGCTTT[C/T]CCAGTGACCACACTG | 4296 |
rs754675221 | snp | A/G | 0.000992556 | 0.0222552 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607271 | GGCCCGGCCCTCACC[A/G]AGTGGCATGCTGATA | 4296 |
rs754694520 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605542 | GAGACTCTGGGCCCC[A/G]AGCCGAGGCCTGGGC | 4296 |
rs754755551 | snp | C/G | 1.65018e-05 | 0.00287239 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608324 | AACCTCAGGAGCCAT[C/G]CAGGCGTAGGTGCCC | 4296 |
rs754846352 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601629 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGAT | 4296 |
rs754982512 | snp | A/G | 1.68117e-05 | 0.00289923 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613607 | ACTGGGCTCGTAGTC[A/G]AACAGGGCTGTCCAC | 4296 |
rs754984608 | snp | C/G/T | 3.38686e-05 | 0.00411502 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607836 | GGGCACGGCGTGCAG[C/G/T]GGGGACAGAATAAGA | 4296 |
rs755026554 | snp | A/G | 5.10991e-05 | 0.0050544 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608228 | ACCTCTGCCCTCTGC[A/G]GCCCCGTAGCAGCCC | 4296 |
rs755028460 | snp | A/C | 1.72707e-05 | 0.00293855 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613785 | CGCTGGGATGTGTGG[A/C]GGACCTTCTCTGGGT | 4296 |
rs755072324 | snp | C/T | 3.3539e-05 | 0.00409492 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607946 | GCTGTGCGAAGGGCT[C/T]GGGGCAGGTGGATGG | 4296 |
rs755116870 | snp | C/G | 1.66635e-05 | 0.00288643 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605787 | GGGGGTGTGGAAGGA[C/G]ATCCTAAGGGGGATG | 4296 |
rs755142176 | snp | C/T | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607684 | AGACCCTGGATCTCG[C/T]GCTTCCAGCCTTCCT | 4296 |
rs755162558 | snp | A/C | 1.70528e-05 | 0.00291995 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613431 | AAGCTGGCCACCTCG[A/C]AGGGGGGCGGGCCGC | 4296 |
rs755204322 | snp | A/G | 7.25804e-05 | 0.0060237 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599578 | GGGGGGTGTTGTCGG[A/G]GACTCCCCGCGCTCG | 4296 |
rs755240746 | snp | C/T | 1.81691e-05 | 0.003014 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613061 | GACGGGCACCAGGGC[C/T]TCGCAGTGCAGGTAG | 4296 |
rs755252434 | snp | A/G | 1.68781e-05 | 0.00290495 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613530 | TCGTCTCCTGAGATG[A/G]CTGCGTCCCGGGACA | 4296 |
rs755366302 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607564 | TGGCACCAATCCCGG[A/C]AGCGCCCGCCCCGAC | 4296 |
rs755382962 | snp | A/G | 1.8697e-05 | 0.00305747 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599416 | CTCCTCCTCACGTCG[A/G]GGGCTCTTGGCTGAC | 4296 |
rs755401328 | snp | C/T | 1.80088e-05 | 0.00300068 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613149 | CGCCCGGCCAGAGCT[C/T]GGCTGAGGGGCCCAC | 4296 |
rs755442392 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598025 | AATTCCCTGAGACAG[C/G]CTCTGGTCCTCCCAA | 4296 |
rs755487787 | snp | A/C | 1.66065e-05 | 0.00288149 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605868 | CTGGTGATGGGAGGG[A/C]AAGGAGGGGTGCTTT | 4296 |
rs755557260 | snp | A/G | 3.26653e-05 | 0.00404124 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598573 | TGGTGAACGTGGGGT[A/G]CCTGGGGTGCCAGGA | 4296 |
rs755558681 | snp | C/T | 1.8039e-05 | 0.00300319 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613138 | GAGGCACGCGCCGCC[C/T]GGCCAGAGCTCGGCT | 4296 |
rs755564740 | in-del | -/TG | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599040 | TGATTACATGTATGC[-/TG]TGTCGCCCAGGCTGG | 4296 |
rs755607002 | snp | C/T | 8.29612e-05 | 0.00644001 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599592 | GGGACTCCCCGCGCT[C/T]GCGTCCTGGGCCTCC | 4296 |
rs755646515 | snp | A/G | 1.93875e-05 | 0.00311342 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607261 | GACGCCCCGGGGCCC[A/G]GCCCTCACCGAGTGG | 4296 |
rs755749106 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604590 | TCTCTCTGTGCCTCA[A/G]TTTTCTCTGTTGTAA | 4296 |
rs755778741 | snp | C/G | 1.84456e-05 | 0.00303685 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598636 | AGTGCCTCCTGTGAG[C/G]ATATAGGAGGGGCAC | 4296 |
rs755791760 | in-del | -/CTT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611173 | CTCCCGTGGTCCCTA[-/CTT]CTCCTTTCTGGGAGG | 4296 |
rs755824405 | snp | C/T | 1.81694e-05 | 0.00301403 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613048 | GATCACGGTGGATGA[C/T]GGGCACCAGGGCCTC | 4296 |
rs755864673 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609797 | GGGCACCTAATACAG[C/T]CTGGTGAGTCAGGGA | 4296 |
rs755874482 | snp | C/T | 0.000102527 | 0.00715913 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598286 | GGGGGAGTGGCCTGG[C/T]CCACTCAAGGCCCCG | 4296 |
rs755903893 | snp | A/C | 1.94998e-05 | 0.00312242 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613686 | CCTCCACCGCCCCCA[A/C]CACCCCCGCTGCCAC | 4296 |
rs755958945 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600475 | TGCGGAGCTGTACAG[C/T]CAGTGAAAGGTGGAG | 4296 |
rs756012515 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612691 | AGAAGATGAGGAGCA[C/T]GAGCTTCCAGAGGAC | 4296 |
rs756065294 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612007 | AAGCCCCTTGTCCAT[C/G]GTCAGCCCAGGCCAG | 4296 |
rs756124082 | snp | A/G | 0.000147973 | 0.00860026 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599644 | AAGGCCCAGCGAGGC[A/G]AGCAGGGCGGTGCCG | 4296 |
rs756165003 | snp | C/G/T | 3.41316e-05 | 0.00413096 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613429 | GGAAGCTGGCCACCT[C/G/T]GCAGGGGGGCGGGCC | 4296 |
rs756174920 | snp | A/G | 1.68741e-05 | 0.00290461 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613626 | AGGGCTGTCCACACC[A/G]GGTTGGCATAACCCG | 4296 |
rs756183843 | snp | A/C | 3.37884e-05 | 0.00411011 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613508 | CACCTGGCCCGCCCA[A/C]CAGCCCTCGTCTCCT | 4296 |
rs756251314 | snp | A/G | 0.000108417 | 0.00736184 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613130 | CACATGGGGAGGCAC[A/G]CGCCGCCCGGCCAGA | 4296 |
rs756339382 | snp | A/G | 7.3959e-05 | 0.00608063 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599504 | TCGGGCGTCTTGAGC[A/G]AGAAGCAGATGAGCG | 4296 |
rs756400101 | snp | A/G | 1.69392e-05 | 0.00291021 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606653 | AGAGAATAAGGAGCT[A/G]GGGGGCGGAGAGGGG | 4296 |
rs756452250 | in-del | -/GCA | 1.87394e-05 | 0.00306094 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607563 | CTGGCACCAATCCCG[-/GCA]GCGCCCGCCCCGACT | 4296 |
rs756537769 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608981 | ATATTTTTCATGTTT[C/T]ACAGATGAGGAAACC | 4296 |
rs756551018 | snp | A/G | 4.70378e-05 | 0.0048494 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598548 | GAGGTCGGCTGATGA[A/G]GCCCAGGGGTGGTGA | 4296 |
rs756631615 | snp | A/C | 3.38341e-05 | 0.00411289 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607826 | AGCAGTCTAGGGGCA[A/C]GGCGTGCAGCGGGGA | 4296 |
rs756651648 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608423 | GTGCTCCATGTCGTC[A/G]CTCTCAATGGGCTGC | 4296 |
rs756714986 | snp | G/T | 2.04761e-05 | 0.00319963 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598529 | CTGCGAAGGGGCGAG[G/T]GCCGAGGTCGGCTGA | 4296 |
rs756724539 | snp | A/G | 1.8181e-05 | 0.00301499 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605727 | CCACGGAAGGAGCTC[A/G]GCCAGATCCTGCCGG | 4296 |
rs756737460 | snp | A/C | 1.67475e-05 | 0.00289369 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606670 | GGGGCGGAGAGGGGC[A/C]TGAGAGGTGAAGTTT | 4296 |
rs756801123 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603379 | TTCCGTGAGGTCTCA[C/T]AGGGAGGACACAGCC | 4296 |
rs756809921 | snp | A/G | 3.63418e-05 | 0.00426258 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613008 | CCCAACCATGCCCCC[A/G]GAAACTCACTGTTGT | 4296 |
rs756856288 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602077 | GCATGGTGGCACGCA[C/T]CTGTAGTCTCAGCTA | 4296 |
rs756864344 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615781 | ATCGTTGGGCGCATG[C/G]GCCACTGCAGGCTGG | 4296 |
rs756868615 | snp | C/G | 9.91522e-05 | 0.00704033 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616278 | CCCCCATGAGGGTCC[C/G]GGGAGGGGGGGCGCG | 4296 |
rs756887799 | snp | C/T | 1.77398e-05 | 0.00297818 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598439 | GTCCAGGGTGCTCGG[C/T]GGGGTGCAGGCTGTG | 4296 |
rs756968953 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603250 | AACATAATCCAGCTA[A/G]GATTTGAATCTGCCT | 4296 |
rs757018256 | snp | C/G | 3.37439e-05 | 0.00410741 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613533 | TCTCCTGAGATGGCT[C/G]CGTCCCGGGACAGCA | 4296 |
rs757033710 | snp | C/G | 1.6855e-05 | 0.00290297 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613622 | GAACAGGGCTGTCCA[C/G]ACCGGGTTGGCATAA | 4296 |
rs757107351 | in-del | -/AGT | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612929 | GGAGCTCCTACCTGC[-/AGT]AGTAGACCCTAAGCT | 4296 |
rs757118521 | snp | A/G | 5.24838e-05 | 0.00512242 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599587 | TGTCGGGGACTCCCC[A/G]CGCTCGCGTCCTGGG | 4296 |