SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15637 | snp | C/G | 0.447291 | 0.153545 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694690 | CAGGCCAGATGCCCC[C/G]ACCGTGTCGTCCATC | 4215 |
rs16421 | in-del | -/AC | 0.486652 | 0.080598 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696160 | CGATCCACAATTCAG[-/AC]ACAGACATAGAGCTG | 4215 |
rs992416 | snp | G/T | 0.363985 | 0.222503 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668545 | ACCATGCTGCCCACC[G/T]CCATCCCCTCAATCT | 4215 |
rs1046229 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695432 | AAGTGTGTGTCGCAT[G/T]CGCCAGTTGGGCCTG | 4215 |
rs1046230 | snp | C/G | 0.0166325 | 0.0896639 | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695499 | CTATCAGCCCCTGTA[C/G]CCCACACTGCCCTCT | 4215 |
rs1046232 | snp | G/T | 0.0198 | 0.0975087 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695902 | CCTCAGGACCAAGTT[G/T]TTGCTTAATTTATTG | 4215 |
rs1060465 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681232 | GTTCTCTACTTGTAT[C/T]AGGTAAAAAGGCCTT | 4215 |
rs1877316 | snp | G/T | 0.403835 | 0.197082 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689520 | GTGCAAGGGCCAGAG[G/T]AGAGCAAGTCACACC | 4215 |
rs2175493 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663715 | gagatgggggtcttg[C/T]tatgttacccaggct | 4215 |
rs2229673 | snp | A/C/G/T | 0.00653701 | 0.0567959 | synonymous-codon, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693594 | GACAGAGAAACCACC[A/C/G/T]TGGGCAGAGTATGAA | 4215 |
rs2319990 | snp | C/T | 0.422158 | 0.181278 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628037 | cagcctccacagtag[C/T]tgggattacaggtgt | 4215 |
rs2874121 | snp | C/T | 0.36315 | 0.222928 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653664 | AAAATCCCTCAATTC[C/T]GTTCTTTTGTTTGCC | 4215 |
rs3785574 | snp | A/G | 0.447291 | 0.153545 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685825 | CAAAACATGTAAAGC[A/G]CTTAGAACAACAAAG | 4215 |
rs3833117 | in-del | -/CA | 0.295088 | 0.245901 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696157 | TCCACAATTCAGACA[-/CA]GACATAGAGCTGGGG | 4215 |
rs4456567 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667729 | TATGATGTAAATACT[A/G]TGTAAATAGTTCTTA | 4215 |
rs6504169 | snp | A/G | 0.355096 | 0.226837 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631785 | TAGGGAGGAAAAACA[A/G]TAGAACTACCCTTTG | 4215 |
rs6504170 | snp | C/T | 0.417034 | 0.18601 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631808 | ACCCTTTGACTTCCC[C/T]ATGGGAAGTAGTAGG | 4215 |
rs6504171 | snp | A/G | 0.400492 | 0.19963 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632650 | GGTCTGTATTTAAGT[A/G]TCTTAGTCCATGTGC | 4215 |
rs6504173 | snp | C/T | 0.447162 | 0.153712 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657696 | TTGTTTTCCTCCAAA[C/T]GTATTTTTATTTTTT | 4215 |
rs6504174 | snp | C/G | 0.363776 | 0.222609 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660777 | ttgtattttttttta[C/G]tagagacggagtttc | 4215 |
rs7206999 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656308 | TTGTGTTTACCATAC[A/G]TGTATAAAATCTgac | 4215 |
rs7209435 | snp | C/T | 0.44768 | 0.153045 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635604 | AGATAGGGTAAGAGG[C/T]AGTGCGGGGAAGATG | 4215 |
rs7211213 | snp | C/T | 0.437259 | 0.165632 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692096 | TCTGAGACTCCCCTT[C/T]GCTAAATCCTTTGCC | 4215 |
rs7212363 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628722 | CTTTTTATCCCTAGA[A/G]TTTGAACACCTTGAA | 4215 |
rs7212379 | snp | A/G | 0.404559 | 0.196498 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628762 | AAAACTTTCTAATGT[A/G]TAATACAAGATAAGT | 4215 |
rs7215530 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63670036 | tgagcctgggaggca[G/T]aggtttcagtgagcc | 4215 |
rs7216798 | snp | A/G | 0.445724 | 0.155538 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663603 | GGATAATGAAGACAC[A/G]GATTTATTCACCTAA | 4215 |
rs7216994 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679513 | tatgagacagggtcg[C/T]actctatcacctatg | 4215 |
rs7217642 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650888 | gtttagtaggcagga[A/G]ggctcactatcttgc | 4215 |
rs7220821 | snp | A/G | 0.447421 | 0.153379 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626787 | AGACTCTCCTGAGTG[A/G]GCAGTGCGATCAGAC | 4215 |
rs7222510 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658898 | cgccaccatgcctgg[A/C]taatttttgtatttt | 4215 |
rs7223672 | snp | C/T | 0.364193 | 0.222396 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643205 | tactaatgtaagata[C/T]taataataggggaaa | 4215 |
rs8064261 | snp | A/G | 0.359575 | 0.224707 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627852 | gcttcccagaatgtt[A/G]gacttacaggtgtga | 4215 |
rs8067438 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677853 | aAAGAAAGAAAGATA[C/G]ATGGCACTGTGCTTC | 4215 |
rs8068007 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662345 | acctgaggccgggag[A/G]ttgaggccgcagtga | 4215 |
rs8068603 | snp | A/T | 0.447032 | 0.153878 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677851 | CCAAAGAAAGAAAGA[A/T]ACATGGCACTGTGCT | 4215 |
rs8069210 | snp | A/G | 0.396546 | 0.202545 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648672 | atacaaaaattagcc[A/G]ggcgtggtggccggc | 4215 |
rs8069553 | snp | C/T | 0.0240643 | 0.107019 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620562 | TTTCCCCTTTATCCC[C/T]GCTTTCAAGAATAGA | 4215 |
rs8070650 | snp | A/G | 0.363776 | 0.222609 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666680 | GCCTGTTATTCCTCC[A/G]TGTCTGGATCATCAC | 4215 |
rs8073373 | snp | C/T | 0.447809 | 0.152878 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625960 | CCCCTATAGTCCCAG[C/T]TACCCAGGAGACCGA | 4215 |
rs8074771 | snp | C/T | 0.363985 | 0.222503 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658505 | GGATTCCTGGAGGCC[C/T]GCATTTCACAAGAAT | 4215 |
rs8075257 | snp | C/G | 0.406641 | 0.194842 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651390 | aggcaggaggattgc[C/G]tgagccccagaggtt | 4215 |
rs8075273 | snp | A/C | 0.363359 | 0.222822 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651521 | ttattatggaaattt[A/C]aagcacacacaaaag | 4215 |
rs8077265 | snp | A/G | 0.447162 | 0.153712 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655367 | caatatgggatttgg[A/G]tggggacacagccaa | 4215 |
rs8080211 | snp | A/G | 0.358521 | 0.225218 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652522 | CTACGTTTTAAGTAT[A/G]CAATTAACCAACCTT | 4215 |
rs8081612 | snp | C/T | 0.446771 | 0.154211 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647335 | TAAATTGTCACTTCA[C/T]TGTTGCTACTTTTCA | 4215 |
rs9891515 | snp | C/T | 0.00107401 | 0.0231485 | synonymous-codon, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692414 | TGGAAGGAAAGCAGA[C/T]GTGTGGTGAGCACTG | 4215 |
rs9892836 | snp | G/T | 0.0648419 | 0.167978 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629048 | GAGAATAAATGATTT[G/T]CTCAGGGCCTCCTTA | 4215 |
rs9894090 | snp | A/G | 0.363776 | 0.222609 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687561 | tgggcatggtggcac[A/G]tgcctgtagtcccag | 4215 |
rs9897006 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675502 | CGTTCAGCTTTAAGT[C/T]AGAGTACAAAGCAAA | 4215 |
rs9899788 | snp | A/G | 0.447032 | 0.153878 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679024 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAGAG | 4215 |
rs9901000 | snp | C/T | 0.363776 | 0.222609 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660438 | agctggtctcaaact[C/T]ctgggctcaagcaat | 4215 |
rs9901112 | snp | C/G | 0.359787 | 0.224604 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653257 | TCTGGGCTGCTTTCC[C/G]AGCTCCAAGAAGAAT | 4215 |
rs9901507 | snp | A/G | 0.445855 | 0.155373 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688164 | GGTAAGAAAGCAGCA[A/G]CCTATCAACGATGAT | 4215 |
rs9902300 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631947 | TACCTTTTAAAGTGT[A/G]CTCTCCTCCTTATGA | 4215 |
rs9902901 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669564 | acccctgcttcatgc[A/G]ctcaagcaattcttc | 4215 |
rs9903897 | snp | A/T | 0.446118 | 0.155041 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639345 | AGAAGCAAACATGGC[A/T]TGTATCAGGAAACAA | 4215 |
rs9903903 | snp | A/G | 0.445592 | 0.155704 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684684 | TTAAACAGAAACAAG[A/G]TCTCACTATGTTGCC | 4215 |
rs9904425 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640823 | CCAGGGAAGAGAGTA[C/T]AGAACTTGATTCTGT | 4215 |
rs9904589 | snp | C/T | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641535 | gccaccacgcccagc[C/T]TAGtgcagttaggtt | 4215 |
rs9906221 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679712 | caaactcctggcctc[A/G]agcatttctcctgcc | 4215 |
rs9908044 | snp | A/C | 0.445855 | 0.155373 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669672 | GTTGGCCAGGCTGGT[A/C]TGACTCCTGACCTCA | 4215 |
rs9909507 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662960 | gattacagttgtgag[C/T]caccacgcccggccC | 4215 |
rs9909992 | snp | A/G | 0.363568 | 0.222716 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654571 | tttcaattctgtaag[A/G]tatatacctaggcgt | 4215 |
rs9910858 | snp | C/G | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691193 | GTCTGCGGGACCGCG[C/G]TGAGAAGACCCTGAC | 4215 |
rs9912201 | snp | A/G | 0.294832 | 0.245947 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685848 | ATGTTTTGACTTTCC[A/G]TATAATATATGCCGC | 4215 |
rs9912523 | snp | G/T | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641920 | GCAGGTTCCCTGTGC[G/T]GGGATAGAGTCACAG | 4215 |
rs9912904 | snp | A/C | 0.363776 | 0.222609 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686174 | CCTCGCCTCTGCCTC[A/C]TTATGCCCAAGAACA | 4215 |
rs9914098 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637329 | ATGTGTATAAGGTTT[A/G]CACAGCTTTTACACA | 4215 |
rs11079508 | snp | C/T | 0.362732 | 0.22314 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672706 | AAGAGGATGAGCCTG[C/T]GAAGGACACAGAAAA | 4215 |
rs11079509 | snp | G/T | 0.191775 | 0.243125 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684788 | GAGCCACCAAGTCTG[G/T]CCCCTATGTAATGTT | 4215 |
rs11327647 | in-del | -/T | 0.407674 | 0.194008 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651429 | AGTGAGCCGTTATCA[-/T]TGCCACTGCACTCCA | 4215 |
rs11558523 | snp | C/G | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696008 | TCCTGGCAGCCCCAG[C/G]CTTGCTGTGGGAAGG | 4215 |
rs11650240 | snp | C/T | 0 | 0 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683626 | CAGCGCCTGCCTCTT[C/T]AGCTGAAGAGAATTG | 4215 |
rs11651118 | snp | A/C | 0.014858 | 0.0849014 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634765 | CACAGTAACAACAAG[A/C]TCATGTGCAGGGGCC | 4215 |
rs11653941 | snp | C/T | 0 | 0 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63695004 | GGGCGCTGGTCCTTT[C/T]TTCCGGCCCCTCCCC | 4215 |
rs11655493 | snp | C/T | 0.363776 | 0.222609 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655692 | gagatgggggtctca[C/T]tattttgcccaggct | 4215 |
rs11655788 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656151 | aggaggatcacttta[G/T]cccaggaggcggagg | 4215 |
rs11655795 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656201 | tgccactgcactcca[G/T]cctgggcaacagagg | 4215 |
rs11656469 | snp | G/T | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659768 | gaactcctgaccttg[G/T]gatccgcccgccttg | 4215 |
rs11657107 | snp | C/T | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627196 | ATTACTTAAAACTGC[C/T]TAAGAGCTTCTACTT | 4215 |
rs11657306 | snp | A/G | 0.441432 | 0.160792 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627462 | TTTTTTTTTTTTTTG[A/G]GGTGGAGTTTTGCCC | 4215 |
rs11658329 | snp | C/G | 0.446118 | 0.155041 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685671 | GAAGAGTTAGCTCTG[C/G]AGGCCCAGGGTTAAA | 4215 |
rs11658584 | snp | C/G | 0 | 0 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686237 | TGGTCAGAGGCTATG[C/G]AAAAGGTTTGGGGAT | 4215 |
rs11658740 | snp | A/G | 0.37138 | 0.218556 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673709 | TGAGGATGGGAGTTC[A/G]AGACCAGCCTGTCCA | 4215 |
rs11871767 | snp | A/G | 0.362941 | 0.223034 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621363 | AAATGTAAGCATACT[A/G]CAAAACAATACAAAG | 4215 |
rs12325866 | snp | A/G | 0.363985 | 0.222503 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678614 | GGAGGCTGGGGTGAT[A/G]TGTCCAAGAAGAGAT | 4215 |
rs12449295 | snp | G/T | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654650 | gattttctataatgg[G/T]tgcacaattttacag | 4215 |
rs12602656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626068 | acaagagtgagagac[C/T]ctgtctctaaaacaa | 4215 |
rs12937046 | snp | A/C | 0 | 0 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657053 | CAGAAAGATAATTAA[A/C]CCGTGCTATGCAGTC | 4215 |
rs12940055 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644782 | GTTTGCTATGTGTTC[C/T]TCATCTTCAAATACT | 4215 |
rs12941889 | snp | A/G | 0.0116955 | 0.0755709 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622337 | GGGTGGGGGTGGTGC[A/G]ACGGCCCAGCGGCTG | 4215 |
rs12946935 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649530 | gctcaagcagtcctc[C/T]tgcctcaacctccca | 4215 |
rs16947005 | snp | A/G | 0.369142 | 0.219784 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625629 | GTTAGAATAGTCTCA[A/G]TTCAGTTTGGCTAGA | 4215 |
rs16947006 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629669 | CTGAAGTATCAGTTG[A/C]AGAACCTGTCTACCT | 4215 |
rs16947009 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632013 | ATAATCCTCTCTCTA[C/T]GGATTCATCTTTTCA | 4215 |
rs16947010 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633337 | ACAGTATTCATATTC[A/G]TTTTTCCCCTTTACT | 4215 |
rs16947014 | snp | C/T | 0.36315 | 0.222928 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641672 | CATTCTTAACAACTA[C/T]ATATTGGCCTCAGAT | 4215 |
rs16947016 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641966 | TTGGCCACCCACCAG[C/T]GTGAAATGCCTCAGA | 4215 |
rs16947025 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657973 | TTCAGGAACTTGTCT[C/T]GCCTCCTTGACAGAC | 4215 |