SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1320327 | snp | A/G | 0.322959 | 0.239117 | intron-variant | KLHL41 | GRCh38.p7 | 2:169524010 | GAATTTTTTTTTTAC[A/G]TATAGTAAGAGGGTC | 10324 |
rs2293058 | snp | C/T | 0.208169 | 0.246476 | intron-variant | KLHL41 | GRCh38.p7 | 2:169514466 | TTACTTGTGAGATAT[C/T]TGACTATCTCGATGA | 10324 |
rs2353190 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL41 | GRCh38.p7 | 2:169522505 | TGAACTAATGAAGGC[C/T]GGGAAGGTTAGGGTT | 10324 |
rs2353191 | snp | C/T | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169522659 | attatatcaaaattt[C/T]tggaggtagagttga | 10324 |
rs3754922 | snp | G/T | 0.0729998 | 0.176553 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169507725 | GTTTAAATATTGTTT[G/T]TTTCAAGCAAAAGAG | 10324 |
rs3754923 | snp | C/T | 0 | 0 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169509090 | attaCAGTTTTTCCA[C/T]GTAAGAATAATTTGG | 10324 |
rs3769771 | snp | C/T | 0.14665 | 0.227637 | intron-variant | KLHL41 | GRCh38.p7 | 2:169511928 | AGGAGTTGGCTTAAC[C/T]TTTGTCTTCCATAAT | 10324 |
rs3769772 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512185 | TTGTGATAATACATA[C/T]TAATCATGTTTCTTA | 10324 |
rs3820954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512060 | AAAGATAAGCAAGTA[C/T]ACAATGTCATACCAC | 10324 |
rs3835903 | in-del | -/CAGA | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169512400 | GATACCTACAAATGA[-/CAGA]TCCACGGAATAGTTG | 10324 |
rs6738934 | snp | A/G | 0.319616 | 0.240112 | intron-variant | KLHL41 | GRCh38.p7 | 2:169521227 | AGAAATCATCTGGGC[A/G]GGCCTGTTTCTTACT | 10324 |
rs6752958 | snp | G/T | 0.111224 | 0.207945 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512288 | TAAAGTCAAATAAAC[G/T]TCAAAAGTGGCAAAG | 10324 |
rs7572182 | snp | A/T | 0.487995 | 0.0765403 | intron-variant | KLHL41 | GRCh38.p7 | 2:169520261 | tccttgggctcaagc[A/T]atcctcctgcctcag | 10324 |
rs7600434 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517559 | CGGTGAGCCAAGATC[A/G]CACCACTGCACTCCA | 10324 |
rs7600451 | snp | G/T | 0.117886 | 0.21224 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517624 | GTCCAGGTCTTTCTG[G/T]TAGCATTTAGCATGT | 10324 |
rs7604374 | snp | A/G | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518774 | tgcctcaaactcctg[A/G]gctcaggtgatcctc | 10324 |
rs7604375 | snp | C/G | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518775 | gcctcaaactcctgg[C/G]ctcaggtgatcctct | 10324 |
rs10206280 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL41 | GRCh38.p7 | 2:169525415 | AGGCACATGCTCATC[C/T]AGACAATGCATATTT | 10324 |
rs10497349 | snp | C/G | 0.137867 | 0.223442 | intron-variant | KLHL41 | GRCh38.p7 | 2:169524998 | TCGTACAAGGGAATT[C/G]AAGTTATCTGTATCT | 10324 |
rs11384512 | in-del | -/T | 0.492386 | 0.0612297 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519651 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 10324 |
rs12692912 | snp | C/T | 0.195214 | 0.243923 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519421 | TAAAAATAATGTTTT[C/T]GAAGACTGTAATGTG | 10324 |
rs12989605 | snp | C/T | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518515 | AAGGAAGTATTTTCA[C/T]CTGGGTTTCTTTTGT | 10324 |
rs13012306 | snp | C/T | 0.143959 | 0.226396 | intron-variant | KLHL41 | GRCh38.p7 | 2:169518097 | AGTTTTCTGATCCTA[C/T]TATATATTTTTCATG | 10324 |
rs13013625 | snp | G/T | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518520 | AGTATTTTCATCTGG[G/T]TTTCTTTTGTTGTTA | 10324 |
rs13387104 | snp | C/T | 0.487871 | 0.076925 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519176 | TAAGCTTTTATTGAC[C/T]TAATGTGAAAAGATA | 10324 |
rs13406673 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL41 | GRCh38.p7 | 2:169514403 | GATTTACTCATTCTT[C/G]TTGGTAATTATGAGC | 10324 |
rs13411178 | snp | A/G | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169516000 | AGATGTTATAACCCA[A/G]AGAGAGGAGAAGTGA | 10324 |
rs13417370 | snp | A/G | 0.47885 | 0.100637 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517081 | ATGAATTTGAAGAAC[A/G]TGATTTTGGATAATG | 10324 |
rs13418086 | snp | C/T | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169517957 | GCTGTGCCTGGGGTT[C/T]TAAGCAGCTATCCAG | 10324 |
rs16856991 | snp | A/T | 0.494296 | 0.0531004 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512899 | CCTTGGTAAGGGAGG[A/T]TTTTTTCCCCCACTC | 10324 |
rs16856992 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL41 | GRCh38.p7 | 2:169513030 | AGTTAAATAGCTTGA[C/T]AGTTCCTCTATAAAA | 10324 |
rs16856998 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | KLHL41 | GRCh38.p7 | 2:169515883 | GTTCAAAACTGAGCT[C/T]CCAGTAGCACCCAGT | 10324 |
rs16857000 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517232 | TGTTTTTCATCACCA[A/G]ATATATCCAGTTAAT | 10324 |
rs16857001 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519561 | GACAAAATTACACCA[A/C]ATTGTTGCTTGTGAT | 10324 |
rs16857003 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | KLHL41 | GRCh38.p7 | 2:169520000 | CCTGTGCTCCTTGAA[C/T]TTTTTTTTCCCCCCT | 10324 |
rs16857008 | snp | C/T | 0.0275645 | 0.114116 | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169526021 | ATCATTAGGGTATCC[C/T]TAAACTGATTTTCTA | 10324 |
rs17524024 | snp | C/T | 0.0919752 | 0.193722 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508867 | TGATAATTTTTGATA[C/T]TTAAAATTACAGATT | 10324 |
rs28718163 | snp | A/G | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169520312 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 10324 |
rs28730867 | snp | C/T | 0.0205432 | 0.0992451 | missense | KLHL41 | GRCh38.p7 | 2:169509786 | CTCACAGAATGGATT[C/T]CCAGCGGGAACTTGC | 10324 |
rs28763868 | snp | A/G | 0.159561 | 0.233068 | missense | KLHL41 | GRCh38.p7 | 2:169510589 | CCTAGCAAAAATGCC[A/G]CGAAGACTGGGGCTG | 10324 |
rs28763869 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL41 | GRCh38.p7 | 2:169511250 | AGATGGGCTCTCACT[A/G]TGTTGCCCCGGCTGG | 10324 |
rs28763870 | snp | A/T | 0.118139 | 0.212397 | intron-variant | KLHL41 | GRCh38.p7 | 2:169514989 | AACTCTCATGATTTA[A/T]GTCTAAATGACTTTT | 10324 |
rs28763871 | snp | C/T | 0.000428449 | 0.0146301 | missense | KLHL41 | GRCh38.p7 | 2:169525631 | ATGTTGAAGGAAATA[C/T]GTTATGCTTCAGGAG | 10324 |
rs28763872 | snp | C/G | 0.0433465 | 0.140692 | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169525848 | TAGGTAAGAAAACCT[C/G]AGTCATTGACTCTTC | 10324 |
rs28763873 | snp | A/G | | | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169525889 | TCAGAGTTTAAAACC[A/G]TTTTCTAATAATAAA | 10324 |
rs34154952 | in-del | -/G | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169517581 | GCACTCCAGCCTGGG[-/G]TGGCAGAGTGAATAA | 10324 |
rs34200400 | in-del | -/G | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169522355 | AGTGGCTATGCAAGG[-/G]AAATTAACTACTTTC | 10324 |
rs34436874 | in-del | -/AT | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518993 | CCTGAATAATTGTCT[-/AT]GTGTAGATGGATATA | 10324 |
rs34623017 | snp | C/T | 0.00413272 | 0.045269 | missense | KLHL41 | GRCh38.p7 | 2:169518254 | AACGAGGAATTTTCA[C/T]TGGAGCCAGATCTTT | 10324 |
rs34630926 | in-del | -/T | | | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508920 | TGTGTGTGGACTTTT[-/T]CGTTCCCTAGATTGA | 10324 |
rs34902501 | in-del | -/C | | | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508159 | CACTCCCACAATCCC[-/C]TGTCTTCATGGAATT | 10324 |
rs35131452 | in-del | -/C | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169522034 | GAAACACAGAATCCC[-/C]AGACCCTACTGAATG | 10324 |
rs35272511 | in-del | -/T | 0.132751 | 0.2208 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508680 | ATAATTAATATGGTA[-/T]TCTATTATAATCAAC | 10324 |
rs35445038 | in-del | -/C | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169512514 | GTCCTTTTTACTTTC[-/C]AAGTGTTCAGTTTAA | 10324 |
rs35560918 | in-del | -/G | | | frameshift-variant | KLHL41 | GRCh38.p7 | 2:169510739 | CTTATGACCCCACGG[-/G]AAAATGAATGCTACC | 10324 |
rs35876311 | in-del | -/A | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169511639 | TGAAAATGAAAAAAA[-/A]CTTGTATATATATTC | 10324 |
rs55969561 | snp | C/T | 0.14665 | 0.227637 | intron-variant | KLHL41 | GRCh38.p7 | 2:169511273 | CCGGCTGGTCTCGAA[C/T]TCCTGGGCTCAAGCA | 10324 |
rs59019005 | in-del | -/GACT | | | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169526167 | TGCCATAAGATGACT[-/GACT]TCAGAAATCCTACTT | 10324 |
rs59155387 | in-del | -/GTGTGTGT | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169520202 | TGTGTGTGTGTGTGT[-/GTGTGTGT]AGACAGTCCATTTTG | 10324 |
rs60605174 | snp | C/T | 0.117537 | 0.212022 | intron-variant | KLHL41 | GRCh38.p7 | 2:169513140 | GTACAGTATGAGAGT[C/T]AAGCCCACAGGTATG | 10324 |
rs60635668 | in-del | -/TTTTTT | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169522732 | TTTTTTTTTTTTTTT[-/TTTTTT]GGTGAGACAGAGTCT | 10324 |
rs71003095 | in-del | -/GTGT | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169520308 | TGTGTGTGTGTGTGT[-/GTGT]ATGTGTGTGTGTGTG | 10324 |
rs71003096 | in-del | -/TTTT | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169522734 | TTTTTTTTTTTTTTT[-/TTTT]GGTGAGACAGAGTCT | 10324 |
rs71430672 | snp | A/C | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512634 | TAACAGAACATTAAC[A/C]ATAACAGTTATACAA | 10324 |
rs71430673 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL41 | GRCh38.p7 | 2:169520483 | TTTAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 10324 |
rs71676328 | in-del | -/AA | 0 | 0 | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169525820 | GAAGTTATTGTCTAA[-/AA]GAGATGAGCAGTAGG | 10324 |
rs72885863 | snp | A/G | 0.0482946 | 0.147699 | utr-variant-3-prime | KLHL41 | GRCh38.p7 | 2:169526204 | TGTAATAAATGGATG[A/G]GGAAATCGTTTGATG | 10324 |
rs73971623 | snp | A/G | 0.0217236 | 0.101931 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508090 | TTCATTCATTCAACA[A/G]ATACTTATAAAGCAC | 10324 |
rs74427695 | snp | G/T | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169515051 | TTTTTTTTTTTTTTT[G/T]AGATGGAGCTTCACT | 10324 |
rs74507153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512706 | AGGCACTAATAGAAC[A/G]GTATGCCAGGATAAA | 10324 |
rs74704359 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | KLHL41 | GRCh38.p7 | 2:169515135 | GCCTCCTGGGTTCAA[C/G]CGATTCTCCTGTCTC | 10324 |
rs74769158 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | KLHL41 | GRCh38.p7 | 2:169524285 | TCTACATAAAAATCA[G/T]TGCATGGTACAATTA | 10324 |
rs74832281 | snp | G/T | | | missense | KLHL41 | GRCh38.p7 | 2:169520949 | GCAATTGGTGGTTTT[G/T]CTATGATTCAACTGG | 10324 |
rs74839160 | snp | C/G | 0.0131998 | 0.0801603 | intron-variant | KLHL41 | GRCh38.p7 | 2:169521034 | TCACTTCAATTTTCA[C/G]AATCACATATTAAAT | 10324 |
rs74901423 | snp | A/T | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169521928 | ATTAAAAAAAAAGTT[A/T]GTTTTTATTTTATTT | 10324 |
rs75034622 | snp | A/G | | | downstream-variant-500B | KLHL41 | GRCh38.p7 | 2:169526390 | AGCATCTGTGGCAGG[A/G]GGGTGAGGGAGCACC | 10324 |
rs75042264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL41 | GRCh38.p7 | 2:169514414 | TCTTCTTGGTAATTA[C/T]GAGCTACAATGTGAT | 10324 |
rs75292431 | snp | G/T | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519667 | TTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA | 10324 |
rs75389244 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517931 | GAATTTAGTAGATAC[A/G]ATTAAAATCAGCTGT | 10324 |
rs75612942 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | KLHL41 | GRCh38.p7 | 2:169511289 | TCCTGGGCTCAAGCA[A/G]TACTCCCAGTTTGGC | 10324 |
rs75847748 | snp | A/T | 0.123105 | 0.215401 | intron-variant | KLHL41 | GRCh38.p7 | 2:169519652 | CAGATTTTCTCAAAC[A/T]TTTTTTTTTTTTTTT | 10324 |
rs75913112 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL41 | GRCh38.p7 | 2:169517694 | GTCTAATCCATAGTC[C/G]CAGATTTCTTAAAAT | 10324 |
rs76033704 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL41 | GRCh38.p7 | 2:169518559 | AAATCTTGTCTAACA[C/T]TCTGATGCATTATAT | 10324 |
rs76074338 | in-del | -/TA | 0.45866 | 0.137698 | intron-variant | KLHL41 | GRCh38.p7 | 2:169518992 | CCCTGAATAATTGTC[-/TA]TGTGTAGATGGATAT | 10324 |
rs76317479 | snp | A/G | 0 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169521924 | GGCTATTAAAAAAAA[A/G]GTTTGTTTTTATTTT | 10324 |
rs76460199 | snp | G/T | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169515049 | TCTTTTTTTTTTTTT[G/T]TGAGATGGAGCTTCA | 10324 |
rs76875207 | snp | C/T | 0.00814182 | 0.0632821 | synonymous-codon | KLHL41 | GRCh38.p7 | 2:169525612 | TAAAAAAGAATGGGC[C/T]GGGATGTTGAAGGAA | 10324 |
rs76926239 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL41 | GRCh38.p7 | 2:169512195 | ACATATTAATCATGT[G/T]TCTTAATTTTCAAAG | 10324 |
rs77322519 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL41 | GRCh38.p7 | 2:169516470 | CTGGTGCCAGATCTT[A/C]TTTTGGGCATTTTTC | 10324 |
rs77643923 | snp | C/T | 0.0573587 | 0.15934 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508636 | TAAACAAAGGACCGA[C/T]TTTCTTTCAAATCAT | 10324 |
rs77956533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL41 | GRCh38.p7 | 2:169524777 | CTCAGATGCCTTTGA[A/G]GCTTGAGGACATTGA | 10324 |
rs78171152 | snp | A/C | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169518992 | GCCCTGAATAATTGT[A/C]TGTGTAGATGGATAT | 10324 |
rs78315335 | snp | C/T | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169523744 | CAAAGCAGCATCAGC[C/T]TCACCTGGGTACTTA | 10324 |
rs78752965 | snp | A/T | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169521764 | TAATTTAAACAGCTT[A/T]CCAATTGTTTTAGGC | 10324 |
rs79518166 | snp | A/G | 0.5 | 0 | intron-variant | KLHL41 | GRCh38.p7 | 2:169522012 | AAGAAAAAAAAAAAA[A/G]GAAAAAAGAAACACA | 10324 |
rs79580851 | snp | A/G | 0.00727717 | 0.0598801 | synonymous-codon | KLHL41 | GRCh38.p7 | 2:169514714 | TTCGCTGGATTCAGT[A/G]TTATGCTATGATCCT | 10324 |
rs79726222 | snp | C/T | 0.117886 | 0.21224 | intron-variant | KLHL41 | GRCh38.p7 | 2:169521903 | CTCAATTGAACATTT[C/T]AGTGAGGCTATTAAA | 10324 |
rs79822311 | snp | G/T | 0.118235 | 0.212457 | intron-variant | KLHL41 | GRCh38.p7 | 2:169511518 | CTGGCAGCTCTAAAT[G/T]GGTCAGATTTTCTAC | 10324 |
rs80054363 | snp | A/C | | | intron-variant | KLHL41 | GRCh38.p7 | 2:169521765 | AATTTAAACAGCTTT[A/C]CAATTGTTTTAGGCT | 10324 |
rs80090638 | snp | A/G | 0.0535932 | 0.154675 | upstream-variant-2KB | KLHL41 | GRCh38.p7 | 2:169508002 | TCACTGTGATGTAAA[A/G]TAAAAGAAAAGGCCT | 10324 |