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 |