SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs143635 | snp | A/G | 0.440978 | 0.16133 | intron-variant | KLHL4 | GRCh38.p7 | X:87621865 | CAGAGCTGACTGTCT[A/G]GTTGGTCTTCAGCCA | 56062 |
rs222063 | snp | A/G | 0.413626 | 0.189014 | intron-variant | KLHL4 | GRCh38.p7 | X:87621515 | TTTTTTTAGTAGAGT[A/G]AAGCTCCTTCTCAAA | 56062 |
rs222064 | snp | G/T | 0.446832 | 0.154134 | intron-variant | KLHL4 | GRCh38.p7 | X:87622734 | CATTTTGCCTAGAAG[G/T]TGTGCAGGAAAAAAA | 56062 |
rs222065 | snp | C/T | 0.425926 | 0.177624 | intron-variant | KLHL4 | GRCh38.p7 | X:87622753 | CTATTGTACTAATTA[C/T]TAACATTTTGCCTAG | 56062 |
rs222066 | snp | A/G | 0.446832 | 0.154134 | intron-variant | KLHL4 | GRCh38.p7 | X:87623208 | TTTGTTATAAAAGTG[A/G]ATTCATGTTAATATT | 56062 |
rs222067 | snp | A/G | 0.425722 | 0.177825 | intron-variant | KLHL4 | GRCh38.p7 | X:87623745 | ATTTCTGTTTTTGGC[A/G]TTACTATTGCCTTCC | 56062 |
rs222068 | snp | C/T | 0.425313 | 0.178229 | intron-variant | KLHL4 | GRCh38.p7 | X:87623912 | CATTTTCAAAGGCAG[C/T]CTGAGAATCTCATAT | 56062 |
rs222069 | snp | A/G | 0.446832 | 0.154134 | intron-variant | KLHL4 | GRCh38.p7 | X:87624136 | GACACTTTCAGCAAA[A/G]TGAACTTAGTTTGAA | 56062 |
rs222070 | snp | A/G | 0.425926 | 0.177624 | intron-variant | KLHL4 | GRCh38.p7 | X:87624279 | ACTTTTCCTGATCGT[A/G]GTAGTGATAGGCAAT | 56062 |
rs222071 | snp | A/G | 0.413846 | 0.188824 | intron-variant | KLHL4 | GRCh38.p7 | X:87624289 | ATCGTAGTAGTGATA[A/G]GCAATGTCATGCAAA | 56062 |
rs222072 | snp | C/T | 0.426536 | 0.177017 | intron-variant | KLHL4 | GRCh38.p7 | X:87624720 | TTGAATTCTCTCCAA[C/T]TCATCTCATGAAAAA | 56062 |
rs222073 | snp | C/T | 0.425926 | 0.177624 | intron-variant | KLHL4 | GRCh38.p7 | X:87626158 | ggggttaagaatggg[C/T]gcattcttaaccttg | 56062 |
rs222074 | snp | C/T | 0.427144 | 0.176408 | intron-variant | KLHL4 | GRCh38.p7 | X:87626446 | tgattgcttcctctg[C/T]tttattgtttatgaa | 56062 |
rs222075 | snp | A/T | 0.355271 | 0.226755 | intron-variant | KLHL4 | GRCh38.p7 | X:87627742 | ACAAGAGAACTAATT[A/T]AAAAATGCAAGTACA | 56062 |
rs222076 | snp | A/C | 0.355271 | 0.226755 | intron-variant | KLHL4 | GRCh38.p7 | X:87627920 | TAAAGGAATGTATTA[A/C]AACAAATGTTTATAA | 56062 |
rs222077 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | KLHL4 | GRCh38.p7 | X:87628282 | ATTCTTATTCAAATA[C/T]GATGTTCCTTTTTCT | 56062 |
rs222078 | snp | A/G | 0.427144 | 0.176408 | intron-variant | KLHL4 | GRCh38.p7 | X:87628327 | ACAGACAAAAGAACA[A/G]CAACAAAACTCTTTG | 56062 |
rs222079 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | KLHL4 | GRCh38.p7 | X:87628340 | GATTCTAAAACCCCA[A/G]AGAGTTTTGTTGCTG | 56062 |
rs222080 | snp | A/C | 0.451394 | 0.148123 | intron-variant | KLHL4 | GRCh38.p7 | X:87630407 | CATTGTGCACATGTA[A/C]CCTAAAACTTAAAGT | 56062 |
rs222081 | snp | A/T | 0.450897 | 0.148796 | intron-variant | KLHL4 | GRCh38.p7 | X:87630430 | GCACAATGTGCAGGT[A/T]TGTTACATATGTATA | 56062 |
rs222082 | snp | C/T | 0.416465 | 0.186519 | intron-variant | KLHL4 | GRCh38.p7 | X:87631815 | TGACCATTCAACATA[C/T]TAATTTATGCTTTTT | 56062 |
rs222083 | snp | A/G | 0.447863 | 0.152807 | intron-variant | KLHL4 | GRCh38.p7 | X:87632124 | ACTGTGCTGTAAGTT[A/G]TGGGTACATAATTAT | 56062 |
rs222084 | snp | A/G | 0.451645 | 0.147782 | synonymous-codon, nc-transcript-variant | KLHL4 | GRCh38.p7 | X:87632244 | ATGTAGCCAACTGTT[A/G]GTCCTGAGGTCATAT | 56062 |
rs222085 | snp | C/T | 0.44332 | 0.158516 | intron-variant | KLHL4 | GRCh38.p7 | X:87634557 | GAATCATGCGAGTTT[C/T]AGACAATAGGTTGGG | 56062 |
rs222086 | snp | A/T | 0.444209 | 0.157426 | intron-variant | KLHL4 | GRCh38.p7 | X:87637102 | tctcgtggaggtggc[A/T]ggggagtgaagtatg | 56062 |
rs222087 | snp | A/G | 0.444562 | 0.156989 | intron-variant | KLHL4 | GRCh38.p7 | X:87637431 | aaaatgaggtttttt[A/G]acatccccaaaagat | 56062 |
rs222088 | snp | A/G | 0.485494 | 0.083921 | intron-variant | KLHL4 | GRCh38.p7 | X:87638153 | aagataaagaaaaaa[A/G]ttattttaaaaaaat | 56062 |
rs222089 | snp | A/G | 0.415597 | 0.187291 | intron-variant | KLHL4 | GRCh38.p7 | X:87639010 | gaaaaaagatagtcc[A/G]tgaaaatggacacaa | 56062 |
rs222090 | snp | A/G | 0.444562 | 0.156989 | intron-variant | KLHL4 | GRCh38.p7 | X:87639082 | aactttaaagcaaca[A/G]cagttaaaaaagaca | 56062 |
rs222091 | snp | A/G | 0.415814 | 0.187098 | intron-variant | KLHL4 | GRCh38.p7 | X:87639173 | atatatatgcaccta[A/G]cactggagctcccaa | 56062 |
rs222092 | snp | C/T | 0.493238 | 0.0577512 | intron-variant | KLHL4 | GRCh38.p7 | X:87639199 | cccaaattcataaaa[C/T]aattactaccagacc | 56062 |
rs222093 | snp | C/T | 0.448375 | 0.152142 | intron-variant | KLHL4 | GRCh38.p7 | X:87639209 | taaaacaattactac[C/T]agacctaagacataa | 56062 |
rs222094 | snp | A/C | 0.449223 | 0.15103 | intron-variant | KLHL4 | GRCh38.p7 | X:87639875 | ttgaaacaacaacaa[A/C]aaaaaaatacaaaag | 56062 |
rs222095 | snp | G/T | 0.48513 | 0.0849334 | intron-variant | KLHL4 | GRCh38.p7 | X:87640493 | aaagataatacacca[G/T]gatcaagttagtttt | 56062 |
rs222096 | snp | C/T | 0.442245 | 0.159818 | intron-variant | KLHL4 | GRCh38.p7 | X:87641176 | tgcaggagcagttag[C/T]tttcttcagatggtc | 56062 |
rs222097 | snp | C/G | 0.4123 | 0.190154 | intron-variant | KLHL4 | GRCh38.p7 | X:87642192 | tgtgaaccatctatg[C/G]gtctctcaacatgga | 56062 |
rs222098 | snp | A/T | 0.483052 | 0.0904795 | intron-variant | KLHL4 | GRCh38.p7 | X:87642552 | ttcagataaatcatg[A/T]atttcttcttggttt | 56062 |
rs222099 | snp | A/T | 0.484297 | 0.0872067 | intron-variant | KLHL4 | GRCh38.p7 | X:87643465 | cagattcacagtgga[A/T]ttctactagacattc | 56062 |
rs222100 | snp | A/T | 0.444209 | 0.157426 | intron-variant | KLHL4 | GRCh38.p7 | X:87645909 | tgggcaagggaagag[A/T]aggaggtagccaggg | 56062 |
rs222101 | snp | A/G | 0.445616 | 0.155675 | intron-variant | KLHL4 | GRCh38.p7 | X:87647509 | tttctttatccactc[A/G]ttgattgataattga | 56062 |
rs222102 | snp | G/T | 0.414286 | 0.188442 | intron-variant | KLHL4 | GRCh38.p7 | X:87648103 | CCAAGATACACACTA[G/T]TCATACAAGTGAGTG | 56062 |
rs222103 | snp | A/G | 0.412964 | 0.189585 | intron-variant | KLHL4 | GRCh38.p7 | X:87649422 | atacatatgataagg[A/G]actaatttccagaat | 56062 |
rs222104 | snp | A/G | 0.41141 | 0.19091 | intron-variant | KLHL4 | GRCh38.p7 | X:87650227 | atgcctgtagcctca[A/G]ctactaaggaggctg | 56062 |
rs222105 | snp | C/T | 0.49779 | 0.0331715 | intron-variant | KLHL4 | GRCh38.p7 | X:87650953 | ccctcatactgttct[C/T]ttgctagtgaatacg | 56062 |
rs222106 | snp | A/G | 0.417974 | 0.185161 | intron-variant | KLHL4 | GRCh38.p7 | X:87652721 | tccaaactttcccac[A/G]ttttcctatcttctt | 56062 |
rs222107 | snp | A/C | 0.497825 | 0.0329083 | intron-variant | KLHL4 | GRCh38.p7 | X:87653175 | gatttgggtgtggac[A/C]tagccaaaccatgtc | 56062 |
rs222108 | snp | C/T | 0.47399 | 0.111034 | intron-variant | KLHL4 | GRCh38.p7 | X:87655110 | aagattctctgttca[C/T]gctatcgattctttc | 56062 |
rs222109 | snp | A/C | 0.497461 | 0.0355386 | intron-variant | KLHL4 | GRCh38.p7 | X:87655623 | gtgtatggtcggatc[A/C]ttttttttaatccat | 56062 |
rs222110 | snp | C/T | 0.421372 | 0.182021 | intron-variant | KLHL4 | GRCh38.p7 | X:87658672 | aaagcaaaagaaacc[C/T]cagattctttgatga | 56062 |
rs222111 | snp | G/T | 0.425926 | 0.177624 | intron-variant | KLHL4 | GRCh38.p7 | X:87659406 | atgaggccgggcatg[G/T]tggctcatgcctgta | 56062 |
rs222112 | snp | A/T | 0.495578 | 0.0468115 | intron-variant | KLHL4 | GRCh38.p7 | X:87666243 | ATATTATCAGAGAGA[A/T]GAAATTTACTTAAGA | 56062 |
rs222113 | snp | A/G | 0.491472 | 0.0647388 | utr-variant-3-prime, intron-variant | KLHL4 | GRCh38.p7 | X:87667086 | CTTTTACTGTGTTGA[A/G]GCTAAAAAAATAATG | 56062 |
rs714535 | snp | A/G | 0.464279 | 0.12878 | intron-variant | KLHL4 | GRCh38.p7 | X:87534085 | CAGGAATAAAAGAAA[A/G]CACGTTTGTTAAATG | 56062 |
rs714536 | snp | A/G | 0.463853 | 0.129486 | intron-variant | KLHL4 | GRCh38.p7 | X:87533936 | AGAACATTGAAACCA[A/G]GTTATTAAGTAAAGG | 56062 |
rs714537 | snp | A/T | 0.34718 | 0.230339 | intron-variant | KLHL4 | GRCh38.p7 | X:87534066 | ACCAAGGTTAAATAC[A/T]CAGCAGGAATAAAAG | 56062 |
rs761313 | snp | C/T | 0.123219 | 0.215468 | intron-variant | KLHL4 | GRCh38.p7 | X:87666086 | CTTTTCAAGATCACA[C/T]GATGAAACAGTGACA | 56062 |
rs968969 | snp | C/T | 0.459151 | 0.136952 | intron-variant | KLHL4 | GRCh38.p7 | X:87576018 | ATGTTAATGAAGTTT[C/T]TATGTTATCACAGTA | 56062 |
rs968970 | snp | C/T | 0.47252 | 0.113952 | intron-variant | KLHL4 | GRCh38.p7 | X:87575860 | TTTGCTTTTTAGCCC[C/T]TCATTTTTAGTTAAA | 56062 |
rs968971 | snp | A/G | 0.49447 | 0.0522912 | intron-variant | KLHL4 | GRCh38.p7 | X:87575842 | ATTTTTAGTTAAATG[A/G]AAGTGAAATCCAAGA | 56062 |
rs1001874 | snp | C/T | 0.460204 | 0.13533 | intron-variant | KLHL4 | GRCh38.p7 | X:87553165 | GCTTTGATAATGTGG[C/T]TAGCTCTGGCGGTTT | 56062 |
rs1155874 | snp | C/T | 0.45384 | 0.144738 | intron-variant | KLHL4 | GRCh38.p7 | X:87543196 | ATTTTATCTGAAACT[C/T]GGTCATTCATAAACA | 56062 |
rs1407000 | snp | G/T | 0 | 0 | intron-variant | KLHL4 | GRCh38.p7 | X:87664544 | GAAGTGCATGGTATC[G/T]TGGAAAGGGAAACTT | 56062 |
rs1575122 | snp | C/T | 0.360916 | 0.224049 | intron-variant | KLHL4 | GRCh38.p7 | X:87656016 | ttgaaaataaaatcc[C/T]agtctcttcttgctt | 56062 |
rs1853088 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | KLHL4 | GRCh38.p7 | X:87640455 | aacacaatactagtt[A/T]acagaatccaacaac | 56062 |
rs2051618 | snp | G/T | 0.479574 | 0.0989738 | intron-variant | KLHL4 | GRCh38.p7 | X:87520868 | AATACCTATATATAT[G/T]ATTTCATAATTAAAT | 56062 |
rs2051622 | snp | C/T | 0.47252 | 0.113952 | intron-variant | KLHL4 | GRCh38.p7 | X:87567505 | gctgttgcacaaata[C/T]ctacttgtccctgct | 56062 |
rs2097487 | snp | A/T | 0.459151 | 0.136952 | intron-variant | KLHL4 | GRCh38.p7 | X:87581757 | agcatttttgtgctg[A/T]ttctttctcatcttt | 56062 |
rs2097488 | snp | G/T | 0.41883 | 0.184381 | intron-variant | KLHL4 | GRCh38.p7 | X:87581683 | atggagtttttctgg[G/T]tttttttgttgtttg | 56062 |
rs2157411 | snp | C/T | 0.460204 | 0.13533 | intron-variant | KLHL4 | GRCh38.p7 | X:87544534 | tcactataaatgtac[C/T]gggtcagacctgaag | 56062 |
rs2157412 | snp | A/C | 0.460204 | 0.13533 | intron-variant | KLHL4 | GRCh38.p7 | X:87544525 | atgtactgggtcaga[A/C]ctgaagccagcacag | 56062 |
rs2179672 | snp | A/G | 0.414066 | 0.188633 | intron-variant | KLHL4 | GRCh38.p7 | X:87604760 | TACATCAAACTGAAA[A/G]GTTTTTTTATAGCAA | 56062 |
rs2187870 | snp | A/G | 0.492084 | 0.0624139 | intron-variant | KLHL4 | GRCh38.p7 | X:87568072 | GTCCTTTTTTTGTAT[A/G]ATTTATTTAACTTAG | 56062 |
rs2206789 | snp | C/T | | | intron-variant | KLHL4 | GRCh38.p7 | X:87626768 | gaaaggaaaataagt[C/T]ttgggacccccaaat | 56062 |
rs2213675 | snp | A/C | 0.450064 | 0.149915 | intron-variant | KLHL4 | GRCh38.p7 | X:87584090 | ggtcttcaacaagat[A/C]tgggagaattctcag | 56062 |
rs2213676 | snp | C/T | 0.451394 | 0.148123 | intron-variant | KLHL4 | GRCh38.p7 | X:87584055 | accaggcagagactt[C/T]tgttccttttccttt | 56062 |
rs2213677 | snp | C/T | 0.349223 | 0.229466 | intron-variant | KLHL4 | GRCh38.p7 | X:87564996 | tttcttttcttgatg[C/T]ctactttcattctga | 56062 |
rs2213678 | snp | G/T | 0.419894 | 0.183401 | intron-variant | KLHL4 | GRCh38.p7 | X:87562671 | tcccttctatcccag[G/T]gtgtgtctagagatg | 56062 |
rs2213679 | snp | A/G | 0.459905 | 0.135794 | intron-variant | KLHL4 | GRCh38.p7 | X:87562617 | atcaggaactttagg[A/G]atatactgtgtactt | 56062 |
rs2213680 | snp | C/T | 0.459604 | 0.136257 | intron-variant | KLHL4 | GRCh38.p7 | X:87560703 | agtcacagcaagata[C/T]gctacatgattccac | 56062 |
rs2213681 | snp | A/T | 0.343348 | 0.231918 | intron-variant | KLHL4 | GRCh38.p7 | X:87560568 | aatctcagttatata[A/T]gaataataagttacg | 56062 |
rs2213682 | snp | A/G | 0.459604 | 0.136257 | intron-variant | KLHL4 | GRCh38.p7 | X:87560414 | AACATATGAAAAATT[A/G]TATCAGCAGCCTGCA | 56062 |
rs2227179 | snp | G/T | 0.492017 | 0.0626724 | intron-variant | KLHL4 | GRCh38.p7 | X:87562813 | ccagcacactatttg[G/T]tttcacccaaggatg | 56062 |
rs2227180 | snp | C/G | 0.0455357 | 0.143855 | intron-variant | KLHL4 | GRCh38.p7 | X:87552767 | actctctatgtccat[C/G]agttccattgattta | 56062 |
rs2273050 | snp | A/C | 0.301751 | 0.244585 | synonymous-codon, nc-transcript-variant | KLHL4 | GRCh38.p7 | X:87622348 | ATTCTGCACATCATG[A/C]CCCACCCACTGCATT | 56062 |
rs2281310 | snp | C/G | 0.307389 | 0.243324 | intron-variant | KLHL4 | GRCh38.p7 | X:87616536 | ATAGTCAAGCCAGCT[C/G]GCTGAATTATCTTAT | 56062 |
rs2281311 | snp | C/T | 0.489036 | 0.0732235 | intron-variant | KLHL4 | GRCh38.p7 | X:87616372 | TAGGGAATATTTTTG[C/T]TTAAAGGCTTGTCAG | 56062 |
rs2294957 | snp | A/C | 0.0127619 | 0.0788547 | intron-variant | KLHL4 | GRCh38.p7 | X:87635816 | TCTAAAAAATTAAAT[A/C]ACCAAATAATTACAT | 56062 |
rs2294958 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | KLHL4 | GRCh38.p7 | X:87634393 | CAAGTGACAGGAAGA[A/G]GTAAATATTCAGGAA | 56062 |
rs2294960 | snp | A/T | 0.017851 | 0.0927731 | intron-variant | KLHL4 | GRCh38.p7 | X:87630378 | GTATAATAATAATTT[A/T]AAAAAAAACCTCATT | 56062 |
rs2294961 | snp | C/G | | | intron-variant | KLHL4 | GRCh38.p7 | X:87619786 | AGAGAGATTAAGAGA[C/G]ACAACAATATTACAT | 56062 |
rs2294962 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | KLHL4 | GRCh38.p7 | X:87619321 | TTTTTAAACAATTGA[A/G]ATTTTAGAAATTAAA | 56062 |
rs2294963 | snp | A/T | 0.430344 | 0.173136 | intron-variant | KLHL4 | GRCh38.p7 | X:87619217 | TTTATGATTTCAATG[A/T]GTGCCTTTCTATTGT | 56062 |
rs2294964 | snp | C/T | 0.413406 | 0.189205 | intron-variant | KLHL4 | GRCh38.p7 | X:87619098 | CACAAAATGATCCAT[C/T]TCTTGTGTCCTTCCC | 56062 |
rs2294965 | snp | C/T | 0.10742 | 0.205356 | intron-variant | KLHL4 | GRCh38.p7 | X:87618646 | GGGCATGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 56062 |
rs2369887 | snp | A/G | 0.450565 | 0.149244 | intron-variant | KLHL4 | GRCh38.p7 | X:87545457 | TACACATGCCCTCTC[A/G]CCTGCTGCCATGTAA | 56062 |
rs2369888 | snp | C/T | 0.34216 | 0.232393 | intron-variant | KLHL4 | GRCh38.p7 | X:87545562 | AATTAAACCACTTTT[C/T]TTCATAAATTACACA | 56062 |
rs2369889 | snp | C/T | 0.450565 | 0.149244 | intron-variant | KLHL4 | GRCh38.p7 | X:87545869 | agaacttattgggaa[C/T]cggtgtaaaggtgac | 56062 |
rs2369890 | snp | A/G | 0.458848 | 0.137414 | intron-variant | KLHL4 | GRCh38.p7 | X:87553900 | ttaattttgtataag[A/G]tgtaaggaagggatc | 56062 |
rs2369891 | snp | G/T | 0.472395 | 0.114194 | intron-variant | KLHL4 | GRCh38.p7 | X:87564249 | ACATTTTAAGATATA[G/T]GTATTATGATAATAT | 56062 |
rs2370007 | snp | C/G | 0.409166 | 0.192785 | intron-variant | KLHL4 | GRCh38.p7 | X:87601564 | GCCCTGAGATCTTAT[C/G]AAGAATCTGCTGATA | 56062 |