SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6663 | snp | C/T | 0.299916 | 0.244966 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448798 | TGCTGTCTTTAGGGC[C/T]CTACCCAAAGTCACT | 83892 |
rs14064 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450760 | CCTTCCTGGAGTGGA[C/G]TCGGGTCAATCAGGA | 83892 |
rs918106 | snp | A/G | 0.498589 | 0.02652 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466513 | TCACAGCCGACATTT[A/G]TGGAGCTCTGTCTAC | 83892 |
rs918107 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466393 | CAGTTATGAATGATA[A/G]TGTTTTGCAGAGTTG | 83892 |
rs961269 | snp | C/T | 0.0402882 | 0.136092 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477338 | CGGCCCCGCCTCCGC[C/T]CCCGGCTGGCGTGAG | 83892 |
rs1045582 | snp | G/T | 0.270621 | 0.249148 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477922 | GTGCTGGGATCTGGC[G/T]TGTGTGCTCCAGGGG | 83892 |
rs1045857 | snp | G/T | 0.121717 | 0.214577 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449017 | GTAATCAAGGGTTTT[G/T]TTTGTTTGTTTGTTT | 83892 |
rs1073779 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456916 | CAGCAATTCTGTTCC[C/T]AGAGAAATGAAAACG | 83892 |
rs1073780 | snp | C/T | 0.198634 | 0.244666 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457338 | TTTCTTTTCAGGCAG[C/T]GAAAAAGTTCTAAAA | 83892 |
rs1477117 | snp | C/T | 0.211516 | 0.24702 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450974 | ATATGGCTGAATGAG[C/T]GTCTAAATCGTTGAG | 83892 |
rs1558804 | snp | C/T | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460927 | CAGGTGAGGCTGCCA[C/T]TCTCCAGGCAGTCCC | 83892 |
rs1990714 | snp | A/C | 0.200492 | 0.245049 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463206 | GCCCTGGGTCTTCCC[A/C]AGCAGCTGAGTTCTG | 83892 |
rs1990715 | snp | A/G | 0.109108 | 0.206518 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462960 | AGAACTGGTAGAAAG[A/G]TAATACGGTCTTTCC | 83892 |
rs2058804 | snp | C/T | 0.244898 | 0.249948 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471206 | TTTACAAAAATAACG[C/T]TTGTGTTTTACCAGT | 83892 |
rs2302703 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461027 | AACAGAGCCTCAGAC[C/T]AGGGTCACCTGGGGT | 83892 |
rs2302704 | snp | C/T | 0.271702 | 0.249056 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460992 | GTTGTGTCCAGCCAG[C/T]AGGGCCTGGAGGCTG | 83892 |
rs2302705 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460911 | TCTCCAGGCAGTCCC[A/G]CTCTCCGCTGGGAGG | 83892 |
rs2302706 | snp | C/T | 0.271944 | 0.249035 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456223 | GTTCATAAAGGATGT[C/T]ATTGGGGATGAAATC | 83892 |
rs2302707 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455992 | TGCCTTGTGATTGCT[C/T]ATCCTTAAAATATTT | 83892 |
rs2302708 | snp | G/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455921 | TGGCATTCCTTTAGC[G/T]CCCTACCTTGCTGGC | 83892 |
rs2302709 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455892 | GCTTCCTTCCAAGCA[C/T]GCTTGACTCCCTGAC | 83892 |
rs2338104 | snp | C/G | 0.497803 | 0.033074 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457363 | ctaaaattagatagt[C/G]gttatggcctcacaa | 83892 |
rs3214388 | in-del | -/A | 0.124491 | 0.216211 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449957 | TGACTGAATGTCAAA[-/A]TCGTGTATTGGGCAG | 83892 |
rs3217162 | in-del | -/GGC | 0.499017 | 0.0221427 | cds-indel, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450354 | TGGGGCACAGGTGGC[-/GGC]CCCTGCTGGAGCCCG | 83892 |
rs3832870 | in-del | -/CCTGAT | 0.212728 | 0.247206 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451899 | TCCCAGGGGCCTGAT[-/CCTGAT]TTAGCCTGGCGGCCC | 83892 |
rs3948619 | snp | G/T | 0.200801 | 0.245111 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474712 | AAGTGGGGGCTGGCT[G/T]TGGTTTATGGTGTTT | 83892 |
rs4766473 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462791 | CTGATTTTTAAAGGA[C/T]GGTAAACTAATTAAA | 83892 |
rs4766474 | snp | C/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470279 | AATGGGATTCCAGCT[C/G]GCACTCCTATCACTT | 83892 |
rs4766475 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470568 | AACTGTAGAGGTGGA[A/G]ATGTGCAAGGGTGGG | 83892 |
rs4766601 | snp | C/G | 0.308661 | 0.24302 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452275 | TGGCCATTTAGGTCA[C/G]TGCTAATATGCTTCT | 83892 |
rs4766602 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452705 | ACAGTGAGTTTACTG[C/T]TTGCTGCTGCCAGCA | 83892 |
rs4766603 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454301 | gagcaaatggaaaca[C/T]agggagtctcagcaa | 83892 |
rs4766604 | snp | C/T | 0.27008 | 0.249192 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454374 | caataaccaacaacc[C/T]caaacaaaaacacaa | 83892 |
rs4766605 | snp | A/C | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457831 | GGGGACCACATGACC[A/C]AATAGCAGGGGCACA | 83892 |
rs6606721 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454194 | ctcacagatgctagc[A/G]ccaaggtgacacaag | 83892 |
rs6606723 | snp | C/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467239 | CAGCTTTTGAAAAAG[C/G]ATTTCACCTCTGAAA | 83892 |
rs6606724 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467374 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 83892 |
rs6606725 | snp | A/C | 0.49975 | 0.0111793 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467563 | GGAGATGGAGGCTGC[A/C]GTGAGCTATGATGGC | 83892 |
rs7136048 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466121 | GGCATGCTCACTGCC[A/G]CAGTGTCCTTGTCTT | 83892 |
rs7139106 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470835 | GCTTTACCAATGAGA[A/G]GTTTAGCCTCCTTCC | 83892 |
rs7295954 | snp | C/T | 0.264084 | 0.249603 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450787 | AGGAGAACAACTGGA[C/T]GGGGCTGGAGTTGGG | 83892 |
rs7298476 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471991 | gaatggagtgtgtag[G/T]cctggaaattgctct | 83892 |
rs7299041 | snp | A/T | 0.242488 | 0.249887 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467223 | CCTTTTCTAGTCCCA[A/T]CAGCTTTTGAAAAAG | 83892 |
rs7308091 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459099 | aacagaatcatcaga[C/G]agttgagagcagata | 83892 |
rs7313797 | snp | C/T | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458360 | TCAAAAATAAACCCT[C/T]GACGTGGCAGCAGAA | 83892 |
rs7315846 | snp | C/T | 0.270351 | 0.24917 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470812 | GGCTAATAGGAGTTA[C/T]AGCTGCTGCTTTACC | 83892 |
rs7316375 | snp | C/G | 0.271702 | 0.249056 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469193 | TGGGGAGCTGAGACT[C/G]AAACCCAGGTTGGCA | 83892 |
rs7959161 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478848 | TTAAATAATCTGTGC[A/G]GTGTCTGATACACCG | 83892 |
rs7967399 | snp | C/T | 0.0792508 | 0.182605 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450402 | ACCCACAGTCACACA[C/T]ATCCCTTAAACAAAC | 83892 |
rs7967695 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463215 | GCTGCTTGGGAAGAC[C/T]CAGGGCCCTGAAATC | 83892 |
rs7969313 | snp | A/G | 0.271972 | 0.249033 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469498 | GCCAGAGGCAGGCAC[A/G]TGGTGGGTGAGCTTA | 83892 |
rs7969549 | snp | C/G | 0.291235 | 0.246576 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461108 | ATATCCCTTACACAA[C/G]GACATCCAACAGGGG | 83892 |
rs7970363 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454527 | tgaggccaggaggtc[A/G]agaccagcctgggca | 83892 |
rs7979038 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473907 | ctgcctcaccctccc[A/G]agtagctgggattac | 83892 |
rs9943689 | snp | A/G | 0.278399 | 0.248382 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452534 | TTCAGGGTGGAATTC[A/G]GAGGTTCTGGGAAAA | 83892 |
rs9943724 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465098 | GGGCAGCATCGCACA[A/G]AGAAACTCCCACGCA | 83892 |
rs9943764 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467915 | TCAGGCCACCAAGGC[A/G]AGGCCTTTCGAGGAG | 83892 |
rs10160889 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463172 | GAAGGAACCTTCCAC[A/G]TTCTGCCTTTGATGT | 83892 |
rs10583123 | in-del | -/TTC | 0.447291 | 0.153545 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466588 | ACATCAACATCCAAG[-/TTC]TTCTTGGTTTAGGAG | 83892 |
rs10774708 | snp | A/G | 0.498346 | 0.0287064 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455351 | ACAGGGGAAATCACC[A/G]CACTATAATTCTGTG | 83892 |
rs10850201 | snp | C/G | 0.256897 | 0.249905 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465257 | ATGTCTGAACGAGAG[C/G]TATTTAGTTGTGGAT | 83892 |
rs10850219 | snp | C/G | 0.251578 | 0.249995 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471709 | GTGAAGACCTCGAAG[C/G]GGGGGAGAAAAGGCT | 83892 |
rs10850234 | snp | A/C | 0.255782 | 0.249933 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476890 | CATTTTCCACCCCCA[A/C]ATGTCCGTTTTCAAT | 83892 |
rs11066686 | snp | C/T | 0.200801 | 0.245111 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457423 | GAATATAATAATAAC[C/T]GTACACTCTAGAAAG | 83892 |
rs11066696 | snp | A/G | 0.20111 | 0.245173 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459346 | TAGACTAACAGAAAC[A/G]AGACCCAGGGGCATG | 83892 |
rs11066707 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460568 | CCCATTTTGCAGAGA[A/G]GGAAAATGAGGAAGG | 83892 |
rs11066714 | snp | C/T | 0.190205 | 0.242744 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461409 | TGACCAAGACAGACC[C/T]CACCCTCAGGCAGCT | 83892 |
rs11066718 | snp | C/G | 0.200801 | 0.245111 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462026 | TCCACGTCCTCCTCA[C/G]ACTGGGCCCTACTGA | 83892 |
rs11066736 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466455 | CACTTGTCCAATGTC[A/G]CATGACCAGTAAATG | 83892 |
rs11066737 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466987 | CTCTCTCCAAGGACC[A/G]ACAGGATCGCTCTGC | 83892 |
rs11066782 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472747 | ACTATCACTGGGCTA[C/T]AGGAATTTTTCAGTT | 83892 |
rs11066788 | snp | C/T | 0.115088 | 0.210473 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473508 | AGCTCTAATGGCAGA[C/T]GGCATGACTAAGAGA | 83892 |
rs11282253 | in-del | -/ATCAGG | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109451905 | CCAGGCTAAATCAGG[-/ATCAGG]CCCCTGGGATTCTGC | 83892 |
rs11540748 | snp | C/T | 0.0517044 | 0.152246 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450895 | GCCACCTTGGGCTGG[C/T]CTTTGGCCTGGTGCT | 83892 |
rs11540749 | snp | A/G | 0.0520825 | 0.152737 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451081 | CTGTGTGTTTGGCCC[A/G]GGCACAATCCCCACT | 83892 |
rs11609019 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458153 | TTGACCGGCTGGACA[A/G]GCTCTGGCGAGGGGA | 83892 |
rs11610840 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456591 | AGTGCTCCTAACCAT[C/T]GTGCTTGAGTGACAG | 83892 |
rs11612500 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459331 | ctggaggtctaacct[C/T]agactaacagaaACG | 83892 |
rs11613021 | snp | G/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460193 | TCTAGAAGCATTTTG[G/T]TTTTGTGGGATTTTA | 83892 |
rs11613023 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460242 | CCAGTGGTCCTGCTC[C/T]GTCTAGCTAAGGAGT | 83892 |
rs11613718 | snp | C/T | 0.271702 | 0.249056 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474527 | CTGATGTAATTGGTC[C/T]GGGATGTGGACTAGG | 83892 |
rs11613809 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469032 | TATCTATCTATCTAT[C/T]TACACACACACATAT | 83892 |
rs11614385 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470049 | ACTGACCCTGCCTGT[A/C]GACCCTGCAGGCACA | 83892 |
rs11615336 | snp | A/C | 0.268452 | 0.249318 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476997 | TTCCTCACGCACACA[A/C]GTATCTACTCCGCAA | 83892 |
rs11615949 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456542 | ATAAATGGCAGACAC[A/G]CCCCCCAAAAGACAG | 83892 |
rs11831213 | snp | C/T | 0.200906 | 0.245132 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457551 | CCTCATCTGAAGGTA[C/T]GAAGAAGAGCTGGGC | 83892 |
rs12227283 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458199 | GCTGGGAAGAGAGAA[A/G]GATTCTCACCACCAG | 83892 |
rs12427319 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451027 | TATCAACAAGCTCTA[A/G]GCCCAAAGCCACATG | 83892 |
rs12578648 | snp | A/G | 0.290201 | 0.246747 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453937 | gcatggcacacagct[A/G]ggacagatttgaagg | 83892 |
rs12582711 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470119 | TGCCTAGCACCTGTA[C/T]ACATGAACACCCTGG | 83892 |
rs12818120 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464111 | TCCTTTCCCCTCTCC[C/T]ACCACCTCCAGGGAA | 83892 |
rs12818537 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464345 | TAAGAGGCTGCCCCG[C/T]ACATTGTAGGGTATT | 83892 |
rs12819142 | snp | G/T | 0.198634 | 0.244666 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458511 | AAAAGTCAAAAATTT[G/T]AGGGTAGAAAGGTCA | 83892 |
rs12819658 | snp | A/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469865 | TTGCTTCCAATGTGG[A/T]CAACTAAGGAGAGCT | 83892 |
rs12819926 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467380 | atcccagcattttgg[A/G]aggctgaggtgagag | 83892 |
rs12821585 | snp | C/T | 0.0520825 | 0.152737 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448556 | CACCTGGAGCGACTT[C/T]AAGGGGCTGAGGCAG | 83892 |
rs12822891 | snp | A/G | 0.271702 | 0.249056 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458197 | TGGCTGGGAAGAGAG[A/G]AGGATTCTCACCACC | 83892 |
rs12822974 | snp | G/T | 0.48 | 0.0979796 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471349 | TGGCACCCAACAGTG[G/T]CCTGGATATCACCTG | 83892 |
rs12823587 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458585 | GGGCGGAAGCACTGG[A/G]AAGATCCCCAAATCC | 83892 |
rs12831026 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465846 | TTCTAGGGGAATGTG[C/T]GATCACAAAATGAAT | 83892 |
rs12833054 | snp | A/G | 0.232067 | 0.249356 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453150 | ACTGCAGCCTTGAAC[A/G]CCTAGGCTCAAATGA | 83892 |
rs16940237 | snp | A/G | 0.0391387 | 0.134304 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450913 | AGCCCAAGGTGGCAA[A/G]AGGCTTGATCCCTAA | 83892 |
rs16940244 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451883 | CACCTGGACTTTAAG[C/G]AGGGCCGCCAGGCTA | 83892 |
rs16940250 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465390 | GGACATGCACAGCTA[C/T]AGTAAGAGTAATACC | 83892 |
rs17180860 | snp | A/G | 0.115088 | 0.210473 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468313 | CTCTTAGGATCAGAG[A/G]ATTAACTGTGGGACA | 83892 |
rs28384415 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-5-prime, splice-donor-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477765 | CTACCCGCAGGCCGA[C/T]CTTTATTCGCCGGAG | 83892 |
rs28384416 | snp | C/G | 0.0659589 | 0.169201 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477378 | CGGGGCGGAAGTGGG[C/G]TGCGGACAGCGGAAG | 83892 |
rs33997929 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474259 | GTTTGATTTCATTAC[C/T]AATGAAGCTGGGGAG | 83892 |
rs34038572 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463852 | AATGCTGGGTCTACC[A/G]ACAGCACTCAAAAGC | 83892 |
rs34225934 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458235 | AGATGGGGGAAGACA[-/G]GGGAGTTGAATTTCC | 83892 |
rs34374622 | in-del | -/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468380 | AAACTCACCCACCCT[-/C]CCCAAGTCAATGTCC | 83892 |
rs34449465 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455799 | GTGGAACGGCATGGT[-/G]GGGAGAAGTCAAAGG | 83892 |
rs34468971 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473783 | TACTGGAATCCTGCT[-/T]TTTTTTTTTTTTTTT | 83892 |
rs34495283 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458128 | CTGCCTAGCACTGCA[-/T]TTTTTAAAGTTGACC | 83892 |
rs34508789 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473479 | AACTATCTTCTCTTT[-/G]GGAAACTGTTTCCAG | 83892 |
rs34538615 | snp | A/C | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474074 | GTGTGAGCCACCGCG[A/C]CTGGCTAATTTTGTA | 83892 |
rs34623703 | in-del | -/T/TT | 0.332106 | 0.236133 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468653 | CAACAATTCTTTGCC[-/T/TT]TTTTTTTTTTTTTTT | 83892 |
rs34639406 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471159 | TCTAGCTTTTCCAGA[-/T]TTTTCTATAATGAAT | 83892 |
rs34650913 | in-del | -/CCG | 0.5 | 0 | cds-indel, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450355 | GGGCTCCAGCAGGGG[-/CCG]CCACCTGTGCCCCAC | 83892 |
rs34714183 | in-del | -/G | 0.498568 | 0.0267188 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459183 | CAAGAAAAGGCTCCT[-/G]GAAGTTAGAAAGACG | 83892 |
rs34737994 | snp | C/T | 0.269809 | 0.249214 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463816 | AATATGATGAAAGAA[C/T]GTACAGAAGGCACAC | 83892 |
rs34768617 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458542 | CAGGTGAGCGTTAAC[C/T]AAGGAGAGGGGGAAA | 83892 |
rs34841752 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461938 | CTTCCTCCCCACTTT[-/G]GGGAGAAGGGCCAAC | 83892 |
rs35018715 | snp | C/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455329 | GCCCTTGACGTGGCG[C/T]GATGGCACAGGGGAA | 83892 |
rs35078783 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468508 | TCTCAGGCCAAGGAA[-/T]GAAGGATGGTACTAT | 83892 |
rs35353200 | snp | A/T | 0.271702 | 0.249056 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458492 | AGGTCAGCAGACCAG[A/T]AAAAAAAGTCAAAAA | 83892 |
rs35388848 | in-del | -/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467293 | CAACAACAGTATCCA[-/C]CCCTCGAAGGGTTAT | 83892 |
rs35422737 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473651 | GGCCCTTGGGGGAAA[A/G]GTTTTGGCAGCATTC | 83892 |
rs35430779 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476647 | GCCCCTGGCATCTCT[-/C]CCCCAGGATTCCAAG | 83892 |
rs35463235 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463862 | CTACCAACAGCACTC[-/A]AAAGCAGCTATGGGT | 83892 |
rs35472007 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470314 | AGGGAGAAGGTGTTT[-/A]CTGAGGACTAAACAA | 83892 |
rs35535701 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470020 | TCCCAAAACCCACCC[-/A]AAAAGCCTCATACAC | 83892 |
rs35590455 | snp | A/G | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455709 | AAAACCCAATTGCAG[A/G]GCCCCAAAAGGGCAG | 83892 |
rs35691073 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471031 | ACCCCAATGCAACAA[-/G]GGAAATAAACCCAAC | 83892 |
rs35725818 | in-del | -/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469395 | CAAGATGGTGGGAGT[-/C]CCCCAACAAGCTGCC | 83892 |
rs35761615 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470564 | TAAAACTGTAGAGGT[-/G]GGAGATGTGCAAGGG | 83892 |
rs35983193 | in-del | -/ACC | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473022 | GACCACTGCATTTCT[-/ACC]ACCACATGCCTTTTA | 83892 |
rs36004776 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472512 | TTACAGTTTTCACTT[-/A]AAAAAAAAAAGGCAG | 83892 |
rs36094325 | snp | A/T | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473737 | CCCCCACCATAGCAA[A/T]CCTCTCTAGGGAGGA | 83892 |
rs36104126 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459859 | AGGGGTATGGTGGTG[-/T]TTTTGATGTTAACCT | 83892 |
rs36118661 | in-del | -/C | 0.269538 | 0.249235 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465180 | CCTCTACATGATCAT[-/C]AACAGAATATGGCTC | 83892 |
rs55816288 | snp | C/T | 0.0670745 | 0.170406 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451308 | CACTTCACACTCATT[C/T]ATACTTTTCCTCTGA | 83892 |
rs55902232 | snp | A/G | 0.269267 | 0.249256 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464500 | AGGTAGATCAAGGAT[A/G]TAAGTGTAAAAAAGC | 83892 |
rs55990265 | snp | C/T | 0.105569 | 0.204058 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472993 | ATGCCTCCAGAAAGC[C/T]CCTCGGTGTCCCTTG | 83892 |
rs56144717 | snp | C/T | 0.269267 | 0.249256 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464499 | GAGGTAGATCAAGGA[C/T]GTAAGTGTAAAAAAG | 83892 |
rs56209061 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467880 | GGGACAGAGGAGTCC[A/G]TTTCTTTTTTGATAT | 83892 |
rs56406401 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462733 | AGCTGTGAGCTCTGA[C/T]GTTCCATGCAATGCC | 83892 |
rs57157733 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462758 | AATGCCAGAAACCCA[A/G]ATTTTTCTGTGAATT | 83892 |
rs57545286 | in-del | -/GTTA | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449073 | AAAAAACTGTAGTTA[-/GTTA]TTACATTGCAATGAA | 83892 |
rs58168448 | snp | C/T | 0.00719014 | 0.0595262 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458049 | GGTGATCACAGGGAC[C/T]TTGCAGAAAGGCTCA | 83892 |
rs58260501 | in-del | -/CAC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473027 | CTGCATTTCTACCAC[-/CAC]ATGCCTTTTACAAAT | 83892 |
rs58383562 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449013 | TTTGAAACAAACAAA[-/C]AAAAAAAACCCTTGA | 83892 |
rs59652081 | in-del | -/CTT | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466593 | AACATCCAAGTTCTT[-/CTT]GGTTTAGGAGTTACT | 83892 |
rs59975102 | snp | A/G | 0.0486741 | 0.148216 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477688 | TGCCCCGGGTCTGGC[A/G]GAACTCGGGTGTTTT | 83892 |
rs59976008 | snp | A/G | 0.109461 | 0.206758 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475242 | ACTTTGGGAGGCTGA[A/G]GCGGGAGGATTGCTT | 83892 |
rs60108170 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479278 | TACAATAAAGCTCAC[-/T]TACATGCTACATGCT | 83892 |
rs60376986 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472531 | AAAAAAAGGCAGGTA[A/G]GAGTATATTCTAAAA | 83892 |
rs61743570 | snp | A/C | 0.472778 | 0.113446 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450809 | GGAGTTGGGGAAAGA[A/C]CCAGAAACAGAGCTG | 83892 |
rs61941572 | snp | C/T | 0.46875 | 0.121031 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461998 | TTCCACTCCTAACAA[C/T]GCTGTGCCCTGTTCC | 83892 |
rs61941582 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463774 | CAGTTTTCTCTTCTA[C/T]AAACGATCTCACAGG | 83892 |
rs61941583 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464136 | AGGGAACCTTCACTG[A/G]CCTCTCTTTGCCATC | 83892 |
rs61941584 | snp | A/G | 0.200801 | 0.245111 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464374 | TTTAGTTGCATCCCT[A/G]GCCTCTACTCACTTG | 83892 |
rs61941585 | snp | C/T | 0.198634 | 0.244666 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467417 | TTGAGCCCAGGAGTT[C/T]GAGGCCAGCCTGGGC | 83892 |
rs61941586 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470927 | CAGCAGCATCCAACA[C/G]AGAGCAAAGCCCCAC | 83892 |
rs61941589 | snp | C/T | 0.20111 | 0.245173 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477051 | CTAACCGCCAGGGAG[C/T]CTCCCTACCACCACC | 83892 |
rs66490142 | in-del | -/TCCTAACAATGCTGTGCCCTGTTCCAC | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461989 | TGTGCCCTGTTCCAC[-/TCCTAACAATGCTGTGCCCTGTTCCAC]GTCCTCCTCAGACTG | 83892 |
rs66539960 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460270 | AGTGAGGGGTGTCTG[C/T]CTGTAGAGATTATGC | 83892 |
rs66704117 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463525 | GTGGGGGGTCTCTCT[C/T]CTGCTGCCACGGGGC | 83892 |
rs66769661 | snp | C/G | 0.0972573 | 0.197913 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464840 | CAAAAATCCAGACTT[C/G]TGCAGGGAGTAGAAG | 83892 |
rs67037059 | in-del | -/A/TA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458492 | GGTCAGCAGACCAGT[-/A/TA]AAAAAAAGTCAAAAA | 83892 |
rs67074557 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463550 | CGGGGCACGAGAGCT[A/G]TTTAGGAAGGCTGTC | 83892 |
rs67329178 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463308 | CGGCTCAAGAATGCC[A/G]TCAGGAAATGCTTGT | 83892 |
rs67668740 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466964 | GCCATGGGTCAGGCT[A/G]TGCAGTGCTCTCTCC | 83892 |
rs67813701 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466723 | CACTTTCTTGGGCAA[C/T]ATGACACATCCCCTG | 83892 |
rs68032303 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462272 | CCCCTGATGAAACAG[C/T]TCAGCCTAAAGTTCC | 83892 |
rs71079564 | in-del | -/C | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467345 | ACCCATCGGCTGTGC[-/C]GTGGGTGGCTCACGC | 83892 |
rs71079565 | in-del | -/G | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467349 | TCGGCTGTGCCGTGG[-/G]TGGCTCACGCCTGTA | 83892 |
rs71443859 | in-del | -/GCTGTGCCCTGTTCCACTCCTAACAAT | 0.299411 | 0.245069 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461972 | TCCACTCCTAACAAC[-/GCTGTGCCCTGTTCCACTCCTAACAAT]GCTGTGCCCTGTTCC | 83892 |
rs71443860 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464499 | GAGGTAGATCAAGGA[CA/TG]TAAGTGTAAAAAAGC | 83892 |
rs71683895 | in-del | -/AC | 0.114387 | 0.210022 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451089 | TTGTGCCCGGGCCAA[-/AC]ACACAGGAACCAGGA | 83892 |
rs72222515 | in-del | -/AAAC | 0.142581 | 0.225746 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449002 | CAGATGGCTTATTTG[-/AAAC]AAACAAACAAAAAAA | 83892 |
rs72647791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460022 | CAGCATTATGGGTAC[C/T]GGTCCGGTGCGGGGC | 83892 |
rs72647792 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460389 | CTGAAGGGTTGAGAT[A/G]TACACATGAGAAGAT | 83892 |
rs72647793 | snp | A/G | 0.00536189 | 0.0514995 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460585 | GAAAATGAGGAAGGC[A/G]GGTAGGCTTGGTGCC | 83892 |
rs72647794 | snp | A/C | 0.00536189 | 0.0514995 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461662 | AGTGGTATTTGTAGA[A/C]GACAGGACTGGAGCC | 83892 |
rs72647795 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462094 | TTGAGAGCAGCAAAC[C/G]CATCTTTTTCACAAT | 83892 |
rs72647796 | snp | A/G | 0.015999 | 0.0879972 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462195 | TCATGGTTTTAGGGC[A/G]TAGTTTGGTATTCTT | 83892 |
rs72647797 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463473 | TCAAATGCCTAGCAC[A/G]TAGAAAGACAAATGG | 83892 |
rs72647798 | snp | C/T | 0.005305 | 0.0512285 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463535 | TCTCTCCTGCTGCCA[C/T]GGGGCACGAGAGCTA | 83892 |
rs72647799 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463665 | ACTTGGGCTCCAGGA[C/T]GTCCTCAGCACAGCA | 83892 |
rs72648060 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465321 | GCAAAACATACAAAC[C/T]GTACAGCACCATTTA | 83892 |
rs72648061 | snp | A/G | 0.116838 | 0.211584 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466631 | ACAGTACAAAACTCA[A/G]TCAGGTAGAAGGGCC | 83892 |
rs72649519 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466739 | ATGACACATCCCCTG[C/T]TCAGGACCTTCAAAG | 83892 |
rs72649520 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467346 | ACCCATCGGCTGTGC[A/G]TGGTGGCTCACGCCT | 83892 |
rs72649521 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467759 | GTGTCCCCCGAGAAC[C/T]TGTGTTTTCCAGGCA | 83892 |
rs73194266 | snp | C/T | 0.121022 | 0.21416 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449720 | AATAGAGCAAGACTC[C/T]GCCTCAAAAAAAAAT | 83892 |
rs73194268 | snp | G/T | 0.0517044 | 0.152246 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449852 | GTATAAAATATTTAC[G/T]AAACATTTTGTAAGC | 83892 |
rs73194269 | snp | A/G | 0.121717 | 0.214577 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450677 | GCTTCATGGGGAAGG[A/G]GGCTGAAGAGGAGCG | 83892 |
rs73194272 | snp | C/T | 0.19459 | 0.243782 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452837 | GGAGGAAATCCTGGT[C/T]TTCTTTCCTTTTTTT | 83892 |
rs73196242 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463592 | CAGCCTGGGATCCCA[C/G]ACCCATTAGGCAAGG | 83892 |
rs73196258 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471517 | GGGGTCTTTGCTGCC[C/G]GATGCCAAACACAAA | 83892 |
rs73196261 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473680 | TCGTGTCCTTGAGCC[C/G]AAGTTACAGTGAACT | 83892 |
rs73407580 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467127 | ATGCCACACTCAAAT[A/G]ATCTGGCCTTGGACC | 83892 |
rs73407581 | snp | A/G | 0.200492 | 0.245049 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467904 | TTGATATGGCATCAG[A/G]CCACCAAGGCGAGGC | 83892 |
rs74509921 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451335 | CTGAGAACCGAGAAA[A/G]CCTGGCTCCAAAGAG | 83892 |
rs74672598 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468536 | TATTTTTAAACCTCA[C/T]GTGACCTGCACGCAA | 83892 |
rs74990107 | snp | C/T | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449025 | AAACAAAAAAAACCC[C/T]TGATTACGACACACC | 83892 |
rs75525576 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457566 | CGAAGAAGAGCTGGG[C/T]CTGGCTGGTGTGAGT | 83892 |
rs75634867 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455928 | AGGTAGGGAGCTAAA[A/G]GAATGCCAGATGAAC | 83892 |
rs75991931 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469016 | TGTGTGTGTGTGTGT[A/G]TATCTATCTATCTAT | 83892 |
rs76026159 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451033 | CAAGCTCTAGGCCCA[A/G]AGCCACATGGCAGAA | 83892 |
rs76110565 | snp | C/T | 0.039522 | 0.134904 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460176 | AAGGGGTGTTGGCCA[C/T]GTCTAGAAGCATTTT | 83892 |
rs76271636 | snp | C/T | 0.0372196 | 0.131242 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448689 | TTTACATGTCGCCAA[C/T]GTTTGTACAACATAC | 83892 |
rs76279190 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461507 | CCAGGCACTGTGAAA[A/C]ATTCTTGGGGGTGGG | 83892 |
rs76359023 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473629 | CAGTCAACCTAATAG[A/T]AGGCAAGGCCCTTGG | 83892 |
rs76929980 | snp | A/C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450251 | CACCCCTGTCAGTCA[A/C/T]GACTCACTCCTGTTC | 83892 |
rs76932709 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458200 | CTGGGAAGAGAGAAG[G/T]ATTCTCACCACCAGT | 83892 |
rs76949522 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475820 | TACATTTCAACTAAA[C/T]TAAGTCACATAATTG | 83892 |
rs76970595 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465033 | AGAGCCCCCTCATTT[C/G]CCAAAGTGAAAATAT | 83892 |
rs76999751 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470725 | ACAGGACCATTCAGT[C/T]ATCATGTCCGGACAC | 83892 |
rs77020148 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470447 | GCTGACTCTCTGTAC[A/C]TCTCAAAGAAATGGA | 83892 |
rs77263283 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475887 | ACCGCCAATTGCAAC[-/TG]TTCCATCAAATGACA | 83892 |
rs77347074 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460072 | TGGGGGAGGCCCAAA[C/T]AAGGGCCTCATGCAC | 83892 |
rs77531759 | snp | A/G | 0.0248432 | 0.108648 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450667 | AGTTAGCCCAGCTTC[A/G]TGGGGAAGGAGGCTG | 83892 |
rs77555099 | in-del | -/GT/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475888 | CCGCCAATTGCAACT[-/GT/TG]TCCATCAAATGACAT | 83892 |
rs77622943 | in-del | -/TAAT | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475539 | ACACCCCAGATCAAT[-/TAAT]CAGTATCTCAGAGAT | 83892 |
rs77732043 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468052 | GCTTCCTCCAGCAGC[A/G]GGGGTGCTATTGTCT | 83892 |
rs77862487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459429 | TGAGACCGCTGAGAA[C/T]GTGGGGCTGAAGTAG | 83892 |
rs77902418 | snp | C/T | 0.067446 | 0.170804 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453654 | TTCTATCTTCATGCT[C/T]CTGGGCCCAAAATAC | 83892 |
rs78160642 | snp | A/C | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479140 | TTATAAAGGACTTGA[A/C]ACATAATGGGCACTC | 83892 |
rs78308831 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472713 | TAATATGTTGTGCTA[A/C]CACTGAAATGACAGC | 83892 |
rs78363306 | snp | C/T | 0.079617 | 0.182947 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464061 | CGCCCCGTGAGCATA[C/T]CATGTGCTTCCTCTC | 83892 |
rs78612465 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459777 | GAATTATGTGGAAAC[A/C]TAAATGTGAACAGAA | 83892 |
rs78650420 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463936 | AGCAGCGTCCAGAGG[A/C]AGCAAGTTCCAGCCC | 83892 |
rs78823865 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451402 | AGCTTGTTCAACGAC[A/G]GGGGTCATACGCCTG | 83892 |
rs78980656 | snp | G/T | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473797 | CTTTTTTTTTTTTTT[G/T]TGAGACTGAGTTTTG | 83892 |
rs79210497 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469859 | AAAAGTTTGCTTCCA[A/T]TGTGGACAACTAAGG | 83892 |
rs79480551 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468095 | ATACTCTCGGGCCAT[A/G]TGGGGTGTGGCACAG | 83892 |
rs79629811 | snp | A/C | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475307 | AAGACCTAATCTCCA[A/C]AAAAAAATTAAAAAA | 83892 |
rs79986796 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468746 | CAAGCTCCGCCTCCC[A/G]AGTTCACGTCATTCT | 83892 |
rs80095910 | snp | C/G | 0.114139 | 0.209862 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469503 | AGGCAGGCACATGGT[C/G]GGTGAGCTTACCTTC | 83892 |
rs80140232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464467 | CCAAAAAATCACCCA[C/T]TGGTTTGGGCATCAC | 83892 |
rs111417005 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454804 | TTTACAAACACAAGA[A/T]CATGCCACTCCTGAA | 83892 |
rs111460893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473288 | GCCCTGAAAATAGTC[A/G]CGAGGTAAAGTGTGG | 83892 |
rs111640453 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449707 | CTCCAGCCTGGCCAA[C/T]AGAGCAAGACTCCGC | 83892 |
rs111648092 | in-del | -/A | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455041 | GAATTCACAGCCCTG[-/A]AAAAAAAAAAAACAG | 83892 |
rs111654961 | snp | C/G | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460893 | GTCTCTCGGCTCCCT[C/G]TACCTCCCAGCGGAG | 83892 |
rs111861366 | snp | C/G/T | 1.65211e-05 | 0.00287407 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457587 | TGGTGTGAGTGGAGG[C/G/T]TTTCCTAGTAAATGG | 83892 |
rs112160404 | snp | A/G | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460326 | ACTAGAGTAAGCCCT[A/G]AGATTGGTCCCGAAC | 83892 |
rs112268691 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478503 | TAGATTATTGAGGCT[A/G]GCCACGGTGGCTCAC | 83892 |
rs112381663 | snp | A/G | 0.5 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469919 | CTTCTCCTAAAATCA[A/G]AGGCCAACTGGGCTA | 83892 |
rs112395120 | snp | C/G | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478896 | GTGGTGGTCATTAAA[C/G]CTGGTGGCCCAGCTT | 83892 |
rs112527688 | snp | C/T | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465402 | CTATAGTAAGAGTAA[C/T]ACCTGGAAAGATGGA | 83892 |
rs112885599 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467569 | GGAGGCTGCCGTGAG[C/T]TATGATGGCCCTAGT | 83892 |
rs112892089 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465295 | ACAAGCATAATGCTA[C/T]GTAAGCAAAAGCAAA | 83892 |
rs113060572 | in-del | -/A | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455405 | TTTCAATAATAAGTT[-/A]AAAAAAAAAAAGACT | 83892 |
rs113277633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453247 | TTTGTAGAGATGAGT[A/G]TGTTGCTATGTTGCC | 83892 |
rs113328172 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449256 | GGCTATAATGCAGCC[A/G]ACAGAATTGTTCACC | 83892 |
rs113518202 | snp | A/C/T | 0.5 | 0 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448550 | CCCTTCCACCTGGAG[A/C/T]GACTTTAAGGGGCTG | 83892 |
rs113551772 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471713 | AGACCTCGAAGGGGG[G/T]GAGAAAAGGCTTACG | 83892 |
rs113579224 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462438 | GTCAACTCCTGGTTT[C/T]AGGGAAGAAAGAGGC | 83892 |
rs113659516 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463294 | GTGACACTGGGCTCC[A/G]GCTCAAGAATGCCGT | 83892 |
rs113868756 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460396 | GTTGAGATGTACACA[A/T]GAGAAGATCCAACAG | 83892 |
rs114047659 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467656 | CCCCATAAAATGCCA[C/T]ACCATTAGCTTTTCA | 83892 |
rs114195395 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460496 | TCCAACCGAAGGAAT[C/T]GGGCTCCAGGGCAAA | 83892 |
rs114523761 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470351 | TGGAAACTTTTGGAA[A/C]CAAGTTATTGCAAAA | 83892 |
rs114677905 | snp | C/T | 0.00332373 | 0.0406302 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460738 | CTCGGGTAAAGGCAC[C/T]GCCCCGTCTCGAAGG | 83892 |
rs114680710 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478150 | TCAGTTTCCTTCTGT[A/G]TAAATGGAGTAATTA | 83892 |
rs115037729 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471946 | GAAGGATTTTTTTCT[A/C]ATGGCATACTTGTAT | 83892 |
rs115107778 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472347 | CACACATTAGCCTAG[C/T]CTACACAGGGTCAGG | 83892 |
rs115208216 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468201 | GCCTGAACAGAAACC[A/G]GAGTTCACAGGAAGC | 83892 |
rs115298427 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461167 | GCCCAAATGGCCACA[A/T]ACCAAGGATAGAAGA | 83892 |
rs115386530 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457307 | AAATGGGGAGTGACT[A/G]CTAACGAATAGAGGG | 83892 |
rs115427006 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468999 | CAAGAAAAAGAAAAA[C/T]GTGTGTGTGTGTGTG | 83892 |
rs115428239 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470581 | GAGATGTGCAAGGGT[A/G]GGCAGAATCTTTGCT | 83892 |
rs115893703 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456997 | ATAGCCAAAAAGTGC[A/G]AACAACCCAAATGTC | 83892 |
rs116195951 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469146 | ATGAGACCAAAAGCT[C/T]CGGCCACTTGGTTAG | 83892 |
rs116479360 | snp | A/C | 0.00432436 | 0.0462977 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460589 | ATGAGGAAGGCAGGT[A/C]GGCTTGGTGCCTCTC | 83892 |
rs117073374 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473704 | GTGAACTTAGGACAC[A/G]AGGCAGTGGACCAGA | 83892 |
rs117112815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467311 | CTCGAAGGGTTATGG[C/T]GAGGATTAAATGAAA | 83892 |
rs117719326 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472553 | ATTCTAAAATAACCA[C/T]TAATAGTAAATACAT | 83892 |
rs117721594 | snp | C/G | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478124 | GGTGAGTTCCCTCAC[C/G]TCTCTGAGCCTCAGT | 83892 |
rs117836348 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453433 | TCCTGGACTCAAGCA[A/G]TCCTTCTGCTTTGGC | 83892 |
rs118106263 | snp | A/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450927 | AAAGGCTTGATCCCT[A/T]AACAAAGCCTTGCAC | 83892 |
rs118134559 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463927 | AAGCAGAGCAGCAGC[A/G]TCCAGAGGCAGCAAG | 83892 |
rs137993541 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449255 | TGGCTATAATGCAGC[C/T]GACAGAATTGTTCAC | 83892 |
rs138116819 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462345 | TCCACTTCCTACTTC[C/T]GCACTGTTCCAATTT | 83892 |
rs138148435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458498 | GCAGACCAGTAAAAA[A/G]AGTCAAAAATTTGAG | 83892 |
rs138205902 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476623 | CGTGGCGCAGGTATC[C/T]TAACCTCAGGCCCCT | 83892 |
rs138293973 | snp | A/C/T | 0.000477885 | 0.0154506 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460718 | TCCTCGATCTCCCGG[A/C/T]GGCTCTCGGGTAAAG | 83892 |
rs138490957 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478551 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 83892 |
rs138503611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457316 | GTGACTGCTAACGAA[C/T]AGAGGGTTTCTTTTC | 83892 |
rs138601206 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461789 | TGAGAGGGTGAAGTC[A/G]AGGCCTTCTGACAAG | 83892 |
rs138669057 | in-del | -/TTTTTTTTTT/TTTTTTTTTTT/TTTTTTTTTTTT/TTTTTTTTTTTTTT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452846 | CCTGGTTTTCTTTCC[lengthTooLong]TTTTTTTTTAAAAGA | 83892 |
rs138697443 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469709 | GCTGAGCTCACCACA[C/G]TTTCTCCTGACATCT | 83892 |
rs138752845 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450252 | ACCCCTGTCAGTCAC[A/G]ACTCACTCCTGTTCC | 83892 |
rs139133763 | in-del | -/AG | 0.0298908 | 0.118541 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450818 | GAAAGAACCAGAAAC[-/AG]AGCTGGACACTTACT | 83892 |
rs139199141 | snp | C/G/T | 0.00296691 | 0.0384022 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469673 | TTGAAGGAAGTGGTG[C/G/T]GGGTAGCAGCCGCTG | 83892 |
rs139231135 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468329 | ATTAACTGTGGGACA[A/C]CAGGCTTAGGTCCCC | 83892 |
rs139260683 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451230 | AGGGAGTGTCACCCA[A/T]AAAGCCCACATAGGA | 83892 |
rs139293157 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448906 | AACTGGGGAATGGGG[A/T]CCCCACACAGTGATC | 83892 |
rs139323097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452234 | AAGGAATTATAAATA[C/T]GACAATGCAATTAAC | 83892 |
rs139378705 | in-del | -/A | 0.271162 | 0.249103 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458491 | AGGTCAGCAGACCAG[-/A]GTAAAAAAAGTCAAA | 83892 |
rs139513754 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479191 | TTGGTTATCACCAAC[C/T]TCTTATTTTCTAATC | 83892 |
rs139657102 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474143 | TGGTCTCGAACTCCC[A/G]ACCTCAAGTGATCCA | 83892 |
rs140308124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465881 | CTTCAATCTAGTGTA[C/T]GCACTAATTCCAAAA | 83892 |
rs140610676 | snp | A/G | 0.000247091 | 0.0111123 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458043 | GGATGAGGTGATCAC[A/G]GGGACCTTGCAGAAA | 83892 |
rs140671662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470095 | CTTGTGTTATAAGCA[C/T]TTCCTTTCTGCCTAG | 83892 |
rs140797979 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455047 | CACAGCCCTGAAAAA[A/C]AAAAAACAGTTCACA | 83892 |
rs140845065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463542 | TGCTGCCACGGGGCA[C/T]GAGAGCTATTTAGGA | 83892 |
rs141129633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475272 | TGAGCCCAGGAATTC[A/G]AGACCAGCCTGAGCA | 83892 |
rs141245326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466658 | GGCCCAGAGCAAAAA[A/G]GAGACTATTCCCCCC | 83892 |
rs141480538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470565 | TAAAACTGTAGAGGT[A/G]GAGATGTGCAAGGGT | 83892 |
rs141482490 | in-del | -/G | 0.00411389 | 0.0451666 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460623 | CCATATGGGAAGAAA[-/G]GGTGATGCCTACTTG | 83892 |
rs141538699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457507 | TCTGTCTACTTATCT[A/C]TCCAGGCAGAGAGGT | 83892 |
rs141720455 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453710 | CAAAGGGGGAATAAC[C/T]AAACCCCCAGCTTTC | 83892 |
rs141810414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463242 | AATCAATTATCCAAA[A/T]GACAGCCCAGAGTTC | 83892 |
rs141827863 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473223 | TGAGAGCTATGATAC[A/G]TAAGCTGAGAAAGGC | 83892 |
rs141898856 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450461 | GTTATCTATCTACCC[A/G]CACATCCTCAACCTG | 83892 |
rs141966647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478374 | ACTGTTTTGGATATA[C/T]ATGGATTCAGATTCA | 83892 |
rs142055908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475115 | TAGTTTCCTTTGGGC[A/G]TCTCAAACATTGGGA | 83892 |
rs142137568 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476139 | CTCCACCCCAAGAAT[A/G]TCTGATTCAGTAGTC | 83892 |
rs142174312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472059 | CATTACTGTACACTA[C/G]TGTAGCTTTATCAAC | 83892 |
rs142297763 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473983 | ATGGGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 83892 |
rs142625906 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451527 | GCCCGGCAGCCTGCA[C/T]AGGATCTGGGTGTAG | 83892 |
rs142636502 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453362 | GCCCAGCTATTTTTT[A/T]AAAAATTTTTGGTAG | 83892 |
rs142662030 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448415 | CCCTCTGCCCCATAA[C/T]AGCAAATCAGTGGTA | 83892 |
rs142936386 | snp | A/T | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478657 | GTGGTGGCGGGCGCC[A/T]TTAATCCCAGCGACT | 83892 |
rs142949365 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464392 | CTCTACTCACTTGAC[A/G]CCAGGAGCACCATCA | 83892 |
rs142982453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463742 | TGACATTGGTGCTTC[A/G]ATTAACCTCTGTCTA | 83892 |
rs143053106 | in-del | -/T | 0.0640965 | 0.167152 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470131 | TATACATGAACACCC[-/T]TGGCTGCACCCTAAA | 83892 |
rs143056773 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461540 | CCAGGAAGACTCCCT[A/G]CTCTGCTGCTCAATG | 83892 |
rs143164188 | in-del | -/G | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475518 | ACCTGTGCTTGCCTG[-/G]GGCTACACCCCAGAT | 83892 |
rs143164208 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466157 | AAAAGCCATCCCTTG[C/G]GGGTAGTGTGGAACT | 83892 |
rs143215691 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448922 | CCCCACACAGTGATC[A/G]CCCCACGGGAGGGTG | 83892 |
rs143237475 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478051 | CGAGGAAAGACTCTG[A/G]GCCCCAGGACTCACC | 83892 |
rs143408771 | snp | A/C | 0.000560621 | 0.0167331 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460765 | AAGGTAGTTGAGTAT[A/C]GTACCAAAGTGCTTC | 83892 |
rs143606895 | snp | A/G | 6.68449e-05 | 0.00578083 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451744 | CATTGTCAGGTCCCC[A/G]GCCATCCTGGGCCTC | 83892 |
rs143669598 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448249 | GCCTCATGGTTTTGC[G/T]TCAAGTCTCAGCTTC | 83892 |
rs143778572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453866 | CCCTAAACTGCATAC[A/G]CAGACTGAAAGAACT | 83892 |
rs143784651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469375 | ATAGCAAATCAACGA[C/T]CAAGTCAAGATGGTG | 83892 |
rs143818969 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465364 | AAACACACCAACAGC[G/T]CCTTGTTTAGGGACA | 83892 |
rs143893351 | snp | C/T | 0.0517044 | 0.152246 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449631 | CTCGGGAGGCTGAGG[C/T]AGCAGAATCGCTTGA | 83892 |
rs143935809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474957 | AACCTGGATTGCAAT[C/T]CAGTTCCACCATTTC | 83892 |
rs144077041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459014 | AAAGCCTCTTTAACA[G/T]GAGAACAAAACCAAA | 83892 |
rs144159923 | in-del | -/TT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468669 | AACAATTCTTTGCCT[-/TT]TTTTTTTTTTTTTTT | 83892 |
rs144374507 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468458 | AGGCGGGGTCAAGGT[C/G]AAGCCAGGCTGTGCC | 83892 |
rs144418618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474338 | AATACTTGAGATACT[A/G]GCTACGGATCTGATT | 83892 |
rs144638888 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460075 | GGGAGGCCCAAACAA[G/T]GGCCTCATGCACACA | 83892 |
rs144879953 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453386 | TTGGTAGAGACAGGG[A/G]TGTTGCTATGTTGCC | 83892 |
rs145217137 | in-del | -/CTCTCGG | 0.0182019 | 0.0936463 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460880 | GCAGAGCTGGGGTGT[-/CTCTCGG]CTCCCTCTACCTCCC | 83892 |
rs145236831 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465921 | AAGACATCAGAAAAC[C/G]TACAATAGGGGGAAG | 83892 |
rs145273683 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475559 | AGTATCTCAGAGATG[C/T]GGAGGGGTGGCTGAT | 83892 |
rs145276519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462213 | GTTTGGTATTCTTTG[C/T]ATGAATTGCCAGGAA | 83892 |
rs145376812 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460488 | GGGGTCACTCCAACC[A/G/T]AAGGAATCGGGCTCC | 83892 |
rs145608794 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470243 | AGCTGCATCACAGAT[G/T]AAATAAGCTTTATGA | 83892 |
rs146261702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458363 | AAAATAAACCCTTGA[C/T]GTGGCAGCAGAAACG | 83892 |
rs146273754 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451042 | GGCCCAAAGCCACAT[A/G]GCAGAAAGCACGTCT | 83892 |
rs146384073 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478453 | TAATATGAATAGTCT[C/T]TTTAAGTCGTGTTTC | 83892 |
rs146394622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474103 | TATTTTTAGTACAGA[C/T]GGGATTTCTCCACAT | 83892 |
rs146438443 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466009 | GCATTGTGAAAGGTG[C/T]TACCTACATCCGTGG | 83892 |
rs146505830 | in-del | -/ACC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473023 | ACCACTGCATTTCTA[-/ACC]CCACATGCCTTTTAC | 83892 |
rs146688900 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465645 | CCACAGGTACAGGTC[A/G]TACTTTATGCCTGGG | 83892 |
rs146748636 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448628 | CCTGGTTATGCCGGG[C/T]ATGCCTGAAAAGAGC | 83892 |
rs146860436 | snp | C/T | 0.00173313 | 0.0293864 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469477 | TCCTTGACCACATAA[C/T]GCATGGCCAGAGGCA | 83892 |
rs146982659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471616 | CACTAACAGTTATGA[C/G]CAGCCACCTCCCTCA | 83892 |
rs147052646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472445 | GAACTGTCATCTCCC[A/G]TAAGAATCCCTTCTT | 83892 |
rs147146623 | snp | C/T | 0.000264127 | 0.0114888 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469690 | GGTAGCAGCCGCTGG[C/T]ACCGCTGAGCTCACC | 83892 |
rs147273737 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459626 | TGAACTGTACTGGGA[A/G]AATGGGAGAAGGAAA | 83892 |
rs147483508 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467658 | CCATAAAATGCCATA[C/G]CATTAGCTTTTCATA | 83892 |
rs147644768 | snp | G/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476096 | TTAGTCTAATCCCTT[G/T]CAGGGCTTGTTAAAA | 83892 |
rs147950601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460155 | GTTGCAACTTTGTTT[C/G]AAATAAAGGGGTGTT | 83892 |
rs147959740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453615 | GCTGTGGTCTCAGCA[A/G]GATTGGGAGAATCTG | 83892 |
rs147977862 | snp | A/C | 4.95913e-05 | 0.00497928 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460785 | CAAAGTGCTTCCCAC[A/C]GCGGTCAATGAGGAT | 83892 |
rs148003422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454703 | CACTGTACTCAAGCC[C/T]GGGTGACAGAGCAAC | 83892 |
rs148118793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472939 | AATACTTGCACCTGT[A/G]TAGCCCCCACTCCAA | 83892 |
rs148277429 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466216 | CAGGCAGCCTCTCCC[A/G]ACATGCTGCTAAGAC | 83892 |
rs148287557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478338 | GCCCTGGATCTTGTT[G/T]GTTTTACTTAGTGAT | 83892 |
rs148531846 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459153 | GCACGCTGTGGAAAG[C/G]AGGGCATTCGGACAG | 83892 |
rs148584954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464099 | ATGTCTGACCTCTCC[A/T]TTCCCCTCTCCCACC | 83892 |
rs148646750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475086 | TTAAAGCATTTGGCA[C/T]CTAGTCCTTTGTGTA | 83892 |
rs149034157 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466068 | GTGAAAATTCTAGCA[C/T]TGTGGGAACTGAACC | 83892 |
rs149176256 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477949 | GGGGCTCTTTCCGCG[A/G]CCCTTTCCACCTCTT | 83892 |
rs149191641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461473 | TGGATATGGAAAAAG[A/G]TCCCAAAGCTGACCA | 83892 |
rs149300529 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463414 | TTGACTTTAAGATAC[C/T]GTGGTTGCTTTCAAA | 83892 |
rs149451813 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449450 | AACACTATGCAGCCA[C/G]GTGTGGTGACTCACA | 83892 |
rs149505184 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458694 | GATTCTGAAAACGGG[C/G]GGACAAGTGAACATC | 83892 |
rs149566138 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468446 | TCAGAAACAGGAAGG[C/G]GGGGTCAAGGTCAAG | 83892 |
rs149672656 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470109 | ACTTCCTTTCTGCCT[A/G]GCACCTGTATACATG | 83892 |
rs149869209 | in-del | -/AAC | 0.191775 | 0.243125 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454096 | GGCCTGGAGTCCTTT[-/AAC]AATATTCAAAATGTT | 83892 |
rs150033200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460478 | AGGCCTCTCAGGGGT[C/G]ACTCCAACCGAAGGA | 83892 |
rs150086300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456930 | CCAGAGAAATGAAAA[C/T]GTAAGTCCACATAGA | 83892 |
rs150147421 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476456 | AGGGACAATGAGCTA[C/T]TCAGGGAACAGACCC | 83892 |
rs150677233 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479101 | TCTTCTCATAGGACT[C/T]CTCTCCTTATTAGAT | 83892 |
rs150844224 | snp | A/G | 0.000301027 | 0.0122647 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451840 | CAGTATACAGGGCAG[A/G]TAAGTTATGGCCCAC | 83892 |
rs150938716 | in-del | -/TAGT | 0.108402 | 0.206034 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449067 | ATTTGTAAAAAACTG[-/TAGT]TAGTTATTACATTGC | 83892 |
rs150960138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469929 | AATCAGAGGCCAACT[A/G]GGCTAGCAGGGGAAC | 83892 |
rs151111292 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448385 | TGTCAAGGGATTGGG[C/T]TTGGTGAACTGAAGC | 83892 |
rs151118344 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465047 | TGCCAAAGTGAAAAT[A/G]TGATTGTCTACGTGC | 83892 |
rs180734233 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464326 | ACCAGATAATTCTTA[C/G]TTGTAAGAGGCTGCC | 83892 |
rs180761449 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475672 | AGCTTTATCTAAGAG[G/T]TGCCAGGGATGTGAG | 83892 |
rs180779987 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451302 | CACATACACTTCACA[C/T]TCATTCATACTTTTC | 83892 |
rs180885385 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456746 | ATCCTCCCTGCATCC[A/C]TCAAGTTCCTGAGTT | 83892 |
rs180980140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469431 | CACATCTTCAGGTCT[C/T]GACTTAAATGTCACT | 83892 |
rs181101303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474704 | ACAAACCAAAACACC[A/G]TAAACCAAAGCCAGC | 83892 |
rs181128271 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451157 | AGCAGGGAGCTCAGA[C/T]ACCTCTGGTGGCCTC | 83892 |
rs181241126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465609 | AGGGAGAGGGACAAA[C/G]AGAGAAGGCACAAAG | 83892 |
rs181622659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469249 | GAGGACAAGGGTCCA[A/G]GGAAGATACCTCTCT | 83892 |
rs181731599 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464393 | TCTACTCACTTGACG[C/G]CAGGAGCACCATCAT | 83892 |
rs181754287 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450551 | TTTATAGCAGGGAAG[C/T]TCCCTGGGGCTGGTG | 83892 |
rs181859730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468624 | AGTAGGAAGTAGTTA[C/T]GACAATGCCCCTCTC | 83892 |
rs182060631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466521 | AGCTCCACAAATGTC[A/G]GCTGTGACTGTGACA | 83892 |
rs182295346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456978 | CATAACAGCATTACA[C/T]ACAATAGCCAAAAAG | 83892 |
rs182369171 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475884 | AGCTACCGCCAATTG[A/C]AACTTCCATCAAATG | 83892 |
rs182400134 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477933 | TGGCGTGTGTGCTCC[A/G]GGGGCTCTTTCCGCG | 83892 |
rs182567414 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452844 | ATCCTGGTTTTCTTT[C/T]CTTTTTTTTTAAAAG | 83892 |
rs182618028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452999 | GTTCAGGAGTGGCGT[A/G]TTCTTGTGTTTGTGA | 83892 |
rs182651562 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454242 | CAAAGACCTGGCAGC[A/G]GCTATTATTAACCTG | 83892 |
rs182761640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458671 | GGTAGAGGACAGGGC[C/T]GAGCTGCGATTCTGA | 83892 |
rs182871483 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450355 | GGGCTCCAGCAGGGG[C/G]CGCCACCTGTGCCCC | 83892 |
rs182930793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457780 | CCCTGCCCTGCATCA[C/G]AAGAGGCAGACAAGC | 83892 |
rs183039701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467261 | CCTCTGAAATGGGGA[C/T]TCCTCACTTGGAATG | 83892 |
rs183174864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470945 | AGCAAAGCCCCACTT[A/C]TCTGAACTGTCTCTC | 83892 |
rs183235402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472050 | GGTCTAGGACATTAC[C/T]GTACACTACTGTAGC | 83892 |
rs183288278 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466594 | ACATCCAAGTTCTTC[G/T]TGGTTTAGGAGTTAC | 83892 |
rs183590203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452646 | CTCAGAAGTAAATCA[C/T]GGCAGGCAGATGGGG | 83892 |
rs183753598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468062 | GCAGCGGGGGTGCTA[A/T]TGTCTTGATTTCCAC | 83892 |
rs183850919 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476198 | TTGAATAAGTTACCA[G/T]GTGTTGCTGCTGGTG | 83892 |
rs183897431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473108 | ATGCCACAGCCCCAT[C/G]AGGGTCAGTCACTCT | 83892 |
rs183961807 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448567 | ACTTTAAGGGGCTGA[A/G]GCAGAACGTGGGGGC | 83892 |
rs184072748 | snp | A/C | 0.000263519 | 0.0114756 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456380 | ATTTGCTGGGCCCTT[A/C]TACACGCAGGGCCCT | 83892 |
rs184191368 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461527 | TTGGGGGTGGGGGCC[A/C]GGAAGACTCCCTACT | 83892 |
rs184445036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455460 | ATTTGCTTTTTGTTC[A/G]AGGTCAGCTACAGAA | 83892 |
rs184450612 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463396 | GAGGTTTCAATCAGC[A/C/G]TTTTGACTTTAAGAT | 83892 |
rs184542040 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477502 | TGGGGAGGGCATTTA[C/T]CCCACCTCCGCTATT | 83892 |
rs184945034 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467616 | GACAGAGAAAGACCC[G/T]GTCTCAAAAAAAGAG | 83892 |
rs185059655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470507 | AGTGAGATTGGTATC[C/T]GGCACATGTGTACTC | 83892 |
rs185124002 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474145 | GTCTCGAACTCCCGA[A/C]CTCAAGTGATCCATC | 83892 |
rs185197165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475457 | ACTCTCCAGCCTGGG[C/T]GACAGAGCAAGACCC | 83892 |
rs185216645 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451250 | CCCACATAGGAAGTC[A/G]ACACCCACAAAAATA | 83892 |
rs185247574 | snp | C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450764 | CCTGGAGTGGAGTCG[C/G]GTCAATCAGGAGAAC | 83892 |
rs185390871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479216 | CTAATCTTTCTACCT[A/G]TATGATTCTTGTTTC | 83892 |
rs185611017 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449498 | TTGGGAGGCCAAGGT[G/T]GTCGGATCACAGGGT | 83892 |
rs185743759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457889 | AACCCATTATCAGGC[C/T]TCACTCAGGCAATTA | 83892 |
rs185784792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473639 | AATAGTAGGCAAGGC[C/T]CTTGGGGGAAAAGTT | 83892 |
rs185805821 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475539 | ACACCCCAGATCAAT[C/T]AATCAGTATCTCAGA | 83892 |
rs186037162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456955 | CATAGAGACTTTGCA[G/T]GAATGTTCATAACAG | 83892 |
rs186038773 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466589 | CATCAACATCCAAGT[A/T]CTTCTTGGTTTAGGA | 83892 |
rs186069799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452751 | ACCCTGAAATGGCAC[C/T]AGGACAGAAGACCTC | 83892 |
rs186086560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464622 | AACAGGATCCAGTAT[A/G]TGAACTTTTGCAAAG | 83892 |
rs186225455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457519 | TCTATCCAGGCAGAG[A/T]GGTACAGAGGGGTCA | 83892 |
rs186227101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466224 | CTCTCCCGACATGCT[A/G]CTAAGACCTGCTTCT | 83892 |
rs186502661 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464386 | CCTGGCCTCTACTCA[C/G]TTGACGCCAGGAGCA | 83892 |
rs186573790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469373 | ACATAGCAAATCAAC[A/G]ACCAAGTCAAGATGG | 83892 |
rs186670967 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476403 | ACAAGCAAGCAAGTA[C/G]AAAGAAGATCTGGGC | 83892 |
rs186702984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448746 | TTTTTTTATGGCGCA[A/C]AGAGACAGAAAGGTT | 83892 |
rs186724147 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465180 | CCTCTACATGATCAT[A/C]AACAGAATATGGCTC | 83892 |
rs186763240 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459185 | AAGAAAAGGCTCCTG[A/G]AGTTAGAAAGACGAA | 83892 |
rs186811317 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466596 | ATCCAAGTTCTTCTT[G/T]GTTTAGGAGTTACTT | 83892 |
rs186883599 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451571 | GGGGGCGGTGAGAGG[A/G]GGGCGGCTCGGTCTC | 83892 |
rs187038622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453734 | AGCTTTCTGGCTGGC[C/T]GATCAGAGAAGGGGA | 83892 |
rs187071131 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477570 | TCCTTCCCGGGCGAA[A/G]AAGCTCTGCGGAACT | 83892 |
rs187186706 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452264 | CCATACTTGGATGGC[C/T]ATTTAGGTCAGTGCT | 83892 |
rs187197222 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448277 | TTCCAAGAACCTATC[A/G]ATGACTTACTGTGCA | 83892 |
rs187390178 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475957 | TCTCTCAATGTTCTA[A/G]TGAGAAAGATGTTTA | 83892 |
rs187402288 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476772 | TGGAAACTCAGCGAC[C/T]CCAGCCACAACCTCC | 83892 |
rs187645493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461086 | TACACTTCTGAAGTA[A/C]CCTCAAATATCCCTT | 83892 |
rs187781728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459537 | AAGAAAATAATCACT[G/T]TACACTCTGTGGCTT | 83892 |
rs187785333 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466649 | AGGTAGAAGGGCCCA[C/G]AGCAAAAAGGAGACT | 83892 |
rs187866016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467699 | GCAGGGGCTGAGCTC[C/T]GGTGACATGAAACAA | 83892 |
rs188213591 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475671 | CAGCTTTATCTAAGA[A/G]TTGCCAGGGATGTGA | 83892 |
rs188296837 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472788 | CTTAAGGGACTGTTA[C/T]ATACGCAGTCTGTCA | 83892 |
rs188564743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467337 | TGAAACAATACCCAT[C/T]GGCTGTGCGTGGTGG | 83892 |
rs188636745 | snp | C/T | 0.21875 | 0.248039 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471312 | GTTATCCAACTCTTC[C/T]GGCCAACTCTCCCCA | 83892 |
rs188722785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474459 | CAGTTGGTGACAATC[A/G]AAATCAGCTGGGAGC | 83892 |
rs188731020 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450956 | ACCCAAAGTTGCACT[A/G]GTCTCAACGATTTAG | 83892 |
rs188867835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479233 | ATGATTCTTGTTTCC[C/G]TAACTAGATTGCAAG | 83892 |
rs188886778 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455700 | AAAAGACAGAAAACC[C/T]AATTGCAGAGCCCCA | 83892 |
rs188941548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455176 | AGTGTTTAGCACTTC[C/T]TGGCTACCTTAAGAA | 83892 |
rs189170472 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477039 | CTTCCCGGATTCCTA[A/C]CCGCCAGGGAGCCTC | 83892 |
rs189229105 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478121 | TTGGGTGAGTTCCCT[C/T]ACCTCTCTGAGCCTC | 83892 |
rs189278473 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464391 | CCTCTACTCACTTGA[A/C/T]GCCAGGAGCACCATC | 83892 |
rs189391348 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463539 | TCCTGCTGCCACGGG[G/T]CACGAGAGCTATTTA | 83892 |
rs189644815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468308 | CAGCCCTCTTAGGAT[C/T]AGAGAATTAACTGTG | 83892 |
rs189659869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456661 | CGAGCCCCAAGAGGA[C/G]CAGAATGGCACTGCC | 83892 |
rs189783797 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451270 | CCACAAAAATAAATA[C/T]TGCAAACAAAAGTTC | 83892 |
rs189955977 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469422 | TGCCTCCTACACATC[C/T]TCAGGTCTCGACTTA | 83892 |
rs190207386 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473930 | GGGATTACAGGCATG[A/C]ACCACCACACCTGGC | 83892 |
rs190310926 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469077 | AATACTGACTATGTG[C/T]CGATGGCCCCACGGG | 83892 |
rs190347605 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470740 | CATCATGTCCGGACA[A/C]AGACAAAAACATAAA | 83892 |
rs190356611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452760 | TGGCACCAGGACAGA[A/C]GACCTCCAGAAGGTC | 83892 |
rs190381349 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476808 | GCCAAACGCTCCGCC[C/T]CAAGGAATCCTACCT | 83892 |
rs190452213 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449697 | TGCCACTACACTCCA[A/G]CCTGGCCAATAGAGC | 83892 |
rs190527405 | snp | C/G/T | 1.75369e-05 | 0.00296111 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451575 | GCGGTGAGAGGAGGG[C/G/T]GGCTCGGTCTCTTGC | 83892 |
rs190560329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456960 | AGACTTTGCATGAAT[A/G]TTCATAACAGCATTA | 83892 |
rs190694988 | snp | C/T | 0.00401592 | 0.0446299 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457593 | GAGTGGAGGTTTTCC[C/T]AGTAAATGGAGCTGT | 83892 |
rs190849761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466811 | GCCTGGCTGAGCTGC[A/G]CTTGGCATTTCTGCC | 83892 |
rs190989397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470552 | TGAAATGAACAGGTA[A/G]AACTGTAGAGGTGGA | 83892 |
rs191100110 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466593 | AACATCCAAGTTCTT[C/G]TTGGTTTAGGAGTTA | 83892 |
rs191124339 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466333 | GAGTTCTCCCAACAT[A/C]TCAGGCCCTGTGGCA | 83892 |
rs191291072 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473334 | TAGACCTGTGCATAA[A/G]GCCCCAGCCCTACCA | 83892 |
rs191297019 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465095 | GCTGGGCAGCATCGC[A/T]CAGAGAAACTCCCAC | 83892 |
rs191388591 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458656 | TGCAGTGGTTTGCAC[A/G]GTAGAGGACAGGGCT | 83892 |
rs191437002 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468019 | AACCACAACAATCCT[C/G]GTTCTCAGATAATGC | 83892 |
rs191451600 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477799 | GGTAGGGCCTGCGGT[C/G]CGGCCTGCGGGAGAA | 83892 |
rs191736875 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448369 | AAATGGAACTCACAT[A/G]TGTCAAGGGATTGGG | 83892 |
rs191774592 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473081 | ATAGTTATTTCCATT[C/T]TGTGGATTTGGATGC | 83892 |
rs191799657 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477738 | TGCGGCCCCGACCCC[A/C]AGTGCGGGGACCTCC | 83892 |
rs191818925 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476090 | AAATCATTAGTCTAA[G/T]CCCTTGCAGGGCTTG | 83892 |
rs191935084 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479339 | TTAATCCTAATCACA[A/G]TGTTGTGATGACTAA | 83892 |
rs191951232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455736 | GCAGGCAAATTCAAT[A/T]AAGGGGGGGCCAGAT | 83892 |
rs192115395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452399 | ACGAAATGGGCATGA[C/G]CCCTTCTGCTGTTTG | 83892 |
rs192116018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461204 | TCTGGGTAAAAAATA[C/T]CTACTTCCTCTTTCC | 83892 |
rs192251818 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450353 | CCGGGCTCCAGCAGG[A/G]GCCGCCACCTGTGCC | 83892 |
rs192401250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454058 | AAACAAAAACATCAA[C/T]GTTCTCCCTAGGATT | 83892 |
rs192901265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462347 | CACTTCCTACTTCCG[C/T]ACTGTTCCAATTTCC | 83892 |
rs193091424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478321 | ATTCTGTGAACGGGG[A/G]AGCCCTGGATCTTGT | 83892 |
rs193138071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459902 | TGACTTCTTGAAGGA[C/T]GCATGTGCATCACTT | 83892 |
rs193166254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474071 | CAGGTGTGAGCCACC[A/G]CGACTGGCTAATTTT | 83892 |
rs193251088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455328 | GGCCCTTGACGTGGC[A/G]TGATGGCACAGGGGA | 83892 |
rs193286364 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448909 | TGGGGAATGGGGTCC[C/G]CACACAGTGATCGCC | 83892 |
rs199651712 | snp | C/T | 1.68949e-05 | 0.0029064 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477225 | GCTCCCTCGGCCGCC[C/T]TCAACCCCTAGTCCA | 83892 |
rs199657965 | snp | A/G | 5.23931e-05 | 0.00511799 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451576 | CGGTGAGAGGAGGGC[A/G]GCTCGGTCTCTTGCC | 83892 |
rs200010361 | snp | C/T | 0.000438101 | 0.0147939 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451700 | GTGGTGGGAGCGCCC[C/T]GCCGCCCCGCCTGTG | 83892 |
rs200111624 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469647 | CGTATTTGGAGCTGG[A/G]GCTCGTGCCCTTGAA | 83892 |
rs200238297 | snp | C/G | 0.000390195 | 0.0139623 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451548 | CTGGGTGTAGCACGG[C/G]AGGGAGTGGGGGCGG | 83892 |
rs200331161 | snp | A/G | 0.000511859 | 0.0159896 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469694 | GCAGCCGCTGGCACC[A/G]CTGAGCTCACCACAC | 83892 |
rs200382460 | in-del | -/TCT | 0.00953873 | 0.0683987 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472286 | CTATAAGCTTTTTTC[-/TCT]TTTTTTACTTTTTAA | 83892 |
rs200524684 | snp | A/G | 0.000395459 | 0.0140561 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456304 | TTTCAACATATTGTC[A/G]TCAGAATTGCTGCAA | 83892 |
rs200627498 | snp | A/C/G | 0.000234362 | 0.0108226 | missense, synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451673 | CCGCTCCCGCTCCTC[A/C/G]TCCTCGTCCAGGTGG | 83892 |
rs200831911 | snp | C/T | 1.67248e-05 | 0.00289173 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451665 | CGCTCGATCCGCTCC[C/T]GCTCCTCGTCCTCGT | 83892 |
rs200838466 | snp | C/G/T | 0.000152131 | 0.00872048 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477241 | TCAACCCCTAGTCCA[C/G/T]GGGCACCGCCCTCCC | 83892 |
rs201000715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460817 | CAGCCTGCAGAGGGA[A/G]GAGGCAGGGGCTGGT | 83892 |
rs201045720 | in-del | -/AATT | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475536 | GCTACACCCCAGATC[-/AATT]AATCAGTATCTCAGA | 83892 |
rs201063803 | snp | A/G | 0.00168136 | 0.0289457 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451631 | GTCATCAGGGCGCTT[A/G]ATGTGGATCCTCCGC | 83892 |
rs201154464 | snp | A/C | 5.01869e-05 | 0.00500909 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460816 | CCAGCCTGCAGAGGG[A/C]GGAGGCAGGGGCTGG | 83892 |
rs201272920 | in-del | -/AAAC | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449433 | TCACACAAACATTTA[-/AAAC]AAACACTATGCAGCC | 83892 |
rs201303040 | snp | C/T | 8.25675e-05 | 0.00642471 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469693 | AGCAGCCGCTGGCAC[C/T]GCTGAGCTCACCACA | 83892 |
rs201485239 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470968 | TGTCTCTCAAATCAC[C/G]CAACACAAGCCCACA | 83892 |
rs201722927 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477237 | GCCCTCAACCCCTAG[A/T]CCATGGGCACCGCCC | 83892 |
rs201876292 | in-del | -/GAT | 0.0134861 | 0.0810011 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449676 | GTTGTGGTAAGTGGA[-/GAT]GATGGTGCCACTACA | 83892 |
rs202019343 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452855 | CTTTCCTTTTTTTTT[A/T]AAAGATATGGGATCT | 83892 |
rs202077179 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469651 | TTTGGAGCTGGGGCT[C/T]GTGCCCTTGAAGGAA | 83892 |
rs202144636 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472512 | ACTTAAAAAAAAAAA[-/A]GGCAGGTAGGAGTAT | 83892 |
rs367627345 | in-del | -/CAA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454098 | CCTGGAGTCCTTTAA[-/CAA]TATTCAAAATGTTTA | 83892 |
rs367648181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475382 | CTCGGGAGACTGCGG[C/T]GGGAGGACTGCTTGA | 83892 |
rs367751021 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450698 | AAGAGGAGCGGGATC[C/T]CAGGGAGGGGTAGTT | 83892 |
rs367786966 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450164 | ACGGTAACGATTCCC[A/T]TGACAAACCCATCCA | 83892 |
rs367916038 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476364 | GATTTTCCCTTAAGA[A/C]TGCACTTTCCAGGGA | 83892 |
rs368114155 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457981 | ATTCCACAAGGGTGC[C/T]TCCAACATACCTTAT | 83892 |
rs368220068 | snp | C/T | 3.38989e-05 | 0.00411683 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469481 | TGACCACATAACGCA[C/T]GGCCAGAGGCAGGCA | 83892 |
rs368352301 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450330 | TCCTACATAGGCGCT[A/G]CGCCCAGCCGGGCTC | 83892 |
rs368398958 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476140 | TCCACCCCAAGAATG[A/T]CTGATTCAGTAGTCT | 83892 |
rs368616071 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469612 | GGTATAGTAGAGGGC[C/T]CCACCCACATTCAGC | 83892 |
rs368703219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474869 | AATCCCTGACCCCAC[A/G]TTTTCTATATGCTTC | 83892 |
rs368752761 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448347 | AAATTTGAATTTTGC[C/T]TTAAATAAATGGAAC | 83892 |
rs368805325 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466143 | CCTTGTCTTCTCAGA[A/G]AAGCCATCCCTTGGG | 83892 |
rs368894886 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477373 | GATAACTTCCGCTGT[C/T]CGCACCCCACTTCCG | 83892 |
rs368927124 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470001 | CATGCATCCCCTAGT[-/G]TTGTCCCAAAACCCA | 83892 |
rs369008333 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473583 | GCAACAAAAGCTCTA[A/C]ACCTTTTCAGAGCTC | 83892 |
rs369011962 | snp | A/C | 8.50391e-05 | 0.00652015 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460610 | GGTGCCTCTCCACCC[A/C]TATGGGAAGAAAGGG | 83892 |
rs369132979 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472466 | ATCCCTTCTTCTGGG[A/T]TACCTCCAGAAGCAC | 83892 |
rs369203016 | snp | A/C/G | 1.73324e-05 | 0.00294379 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451581 | AGAGGAGGGCGGCTC[A/C/G]GTCTCTTGCCTGCTC | 83892 |
rs369239008 | snp | C/T | 0.000152229 | 0.00872303 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477256 | TGGGCACCGCCCTCC[C/T]TACCATGAAAAGTCG | 83892 |
rs369423726 | snp | A/G | 5.03487e-05 | 0.00501715 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451709 | GCGCCCCGCCGCCCC[A/G]CCTGTGGCCTCCAGG | 83892 |
rs369597796 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468738 | GCTCACTGCAAGCTC[C/T]GCCTCCCGAGTTCAC | 83892 |
rs369619684 | snp | A/C | 1.76437e-05 | 0.00297011 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469762 | CAGGGTCATGACATC[A/C]GGCCTGGTTGACTGC | 83892 |
rs369655321 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466736 | AACATGACACATCCC[C/T]TGTTCAGGACCTTCA | 83892 |
rs369728531 | snp | A/C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477130 | CCCCTAACCAATCCC[A/C/G]CAAATGCCTCTCCAC | 83892 |
rs369957720 | snp | C/T | 6.67568e-05 | 0.00577702 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451648 | TGTGGATCCTCCGCA[C/T]GCGCTCGATCCGCTC | 83892 |
rs369991060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469148 | GAGACCAAAAGCTTC[A/G]GCCACTTGGTTAGGA | 83892 |
rs370026383 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463604 | CCAGACCCATTAGGC[A/G]AGGCTGGAGAGCAGA | 83892 |
rs370059628 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450738 | TGCCTGTCACAGGGT[C/T]AGATGGCCTTCCTGG | 83892 |
rs370067670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479289 | TCACTTACATGCTAC[A/G]TGCTTTTAGATATCC | 83892 |
rs370261251 | in-del | -/CAA | | | cds-indel, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449013 | TTTGAAACAAACAAA[-/CAA]AAAAAACCCTTGATT | 83892 |
rs370555225 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469472 | AGCCCTCCTTGACCA[C/T]ATAACGCATGGCCAG | 83892 |
rs370700067 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464439 | AAAATGTCTCTGGAC[A/G]TTGCTAAATATCCCA | 83892 |
rs370701913 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456073 | AAGTTCTATAGGTGT[A/G]TGTTTCAGAACAGCC | 83892 |
rs370961325 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455740 | GCAAATTCAATTAAG[C/G/T]GGGGGCCAGATCTCT | 83892 |
rs370963521 | snp | A/G | 3.39593e-05 | 0.0041205 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469478 | CCTTGACCACATAAC[A/G]CATGGCCAGAGGCAG | 83892 |
rs370979496 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449425 | ACTCATTCTTCACAC[A/G]AACATTTAAAACACT | 83892 |
rs370992279 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478085 | ACTGGAGTTCGAATA[C/G]TGTTCGCTCGCTGTG | 83892 |
rs371008807 | in-del | -/AT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456941 | AAAACGTAAGTCCAC[-/AT]AGAGACTTTGCATGA | 83892 |
rs371077296 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475145 | ATCAGTGGTTCCCAA[C/T]CCTGGCTACTAGAAT | 83892 |
rs371120625 | snp | A/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456311 | ATATTGTCGTCAGAA[A/T]TGCTGCAAAAGAGCA | 83892 |
rs371254100 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459245 | GAAAAGGTGAAAAAT[A/G]AAACTTCTGAGAAAG | 83892 |
rs371507611 | snp | C/G | 3.42759e-05 | 0.00413966 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451589 | GCGGCTCGGTCTCTT[C/G]CCTGCTCACTGGTGG | 83892 |
rs371576340 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450223 | TAACTACTCTACCTA[A/G]TCTAGTCTCAACCAC | 83892 |
rs371590722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478839 | ACAAGTTGGTTAAAT[A/C]ATCTGTGCAGTGTCT | 83892 |
rs371668991 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450954 | GCACCCAAAGTTGCA[C/T]TGGTCTCAACGATTT | 83892 |
rs371723039 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462093 | GTTGAGAGCAGCAAA[C/T]GCATCTTTTTCACAA | 83892 |
rs371744289 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468585 | GGAGCCCTGTTGTCA[A/G]GGGCTCTTTGATCAT | 83892 |
rs371857757 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455688 | ATTAAAAGTTTAAAA[-/A]GACAGAAAACCCAAT | 83892 |
rs372039639 | snp | C/G | 1.64846e-05 | 0.0028709 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457613 | AATGGAGCTGTCTTT[C/G]CCGGCTGACGCCTTA | 83892 |
rs372156933 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452840 | GGAAATCCTGGTTTT[C/T]TTTCCTTTTTTTTTA | 83892 |
rs372222827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475576 | GAGGGGTGGCTGATC[A/G]GTCACTAGTGTTTAA | 83892 |
rs372312574 | snp | C/T | 0.000131904 | 0.00812002 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460690 | TAGGTAGTACTTGGC[C/T]TCTGCTAGCAGCTCC | 83892 |
rs372349700 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467805 | CATCTCATAGCAGGG[A/T]TTTAGAAGGTGAGCA | 83892 |
rs372647219 | snp | A/G | 4.94287e-05 | 0.00497111 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469633 | CACATTCAGCTTCAC[A/G]TATTTGGAGCTGGGG | 83892 |
rs372732204 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468051 | TGCTTCCTCCAGCAG[C/T]GGGGGTGCTATTGTC | 83892 |
rs372840457 | in-del | -/CA | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451094 | CCCGGGCCAAACACA[-/CA]GGAACCAGGAGTGGA | 83892 |
rs373127599 | snp | C/T | 6.76865e-05 | 0.0058171 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477248 | CTAGTCCATGGGCAC[C/T]GCCCTCCCTACCATG | 83892 |
rs373238395 | snp | A/G | 6.80863e-05 | 0.00583425 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469468 | GGGAAGCCCTCCTTG[A/G]CCACATAACGCATGG | 83892 |
rs373283832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466612 | GTTTAGGAGTTACTT[A/G]CACACAGTACAAAAC | 83892 |
rs373360499 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477068 | TCCCTACCACCACCC[A/C]CGCCCCTAATTCTCC | 83892 |
rs373496812 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460362 | CCAAGTTTCACACCG[C/T]GGGGTTCTCTGCTGA | 83892 |
rs373511372 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449718 | CCAATAGAGCAAGAC[C/T]CCGCCTCAAAAAAAA | 83892 |
rs373526310 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472087 | AACACTGCACAGGGA[G/T]GCCACACTACATTTA | 83892 |
rs373694579 | snp | A/C/G | 3.2961e-05 | 0.00405951 | synonymous-codon, stop-gained, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458064 | CTTGCAGAAAGGCTC[A/C/G]TAAGTATCTTTGTTC | 83892 |
rs373756424 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452589 | TCTTCCTCACTGACA[C/T]TACAAAGCCAGAATG | 83892 |
rs373772372 | snp | A/G | 0.000248277 | 0.011139 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456107 | CCAAACTGTCCTCTC[A/G]AGGCTCTTACCTTGG | 83892 |
rs373818598 | snp | A/G | 3.39132e-05 | 0.0041177 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451696 | CCAGGTGGTGGGAGC[A/G]CCCCGCCGCCCCGCC | 83892 |
rs373859718 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477677 | GCGTCGGCTGCTGCC[C/T]CGGGTCTGGCAGAAC | 83892 |
rs373943437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455063 | AAAAAACAGTTCACA[A/G]GAGAAAAGGGGCATG | 83892 |
rs373984653 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453461 | GGCCTCCCAAAGTGC[A/G]GGATTACAGGTGTGA | 83892 |
rs374028626 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465122 | CCACGCACGGGGAAA[A/G]CGTTCAAGGATGTTC | 83892 |
rs374083574 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452845 | TCCTGGTTTTCTTTC[C/T]TTTTTTTTTAAAAGA | 83892 |
rs374139033 | snp | A/G | 7.53452e-05 | 0.00613734 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451827 | ACCTGTGTTCCCACA[A/G]TATACAGGGCAGGTA | 83892 |
rs374242009 | snp | C/T | 0.000263648 | 0.0114784 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457723 | AAGAGAGTTACTTGG[C/T]AGGCAGATGCAATGA | 83892 |
rs374251027 | snp | C/T | 9.88973e-05 | 0.00703128 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460715 | AGCTCCTCGATCTCC[C/T]GGCGGCTCTCGGGTA | 83892 |
rs374288492 | snp | C/T | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448487 | ACCCCAAGACTTCCT[C/T]TTGGTGTTTGAATTC | 83892 |
rs374339959 | snp | A/G | 1.66147e-05 | 0.0028822 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469721 | ACACTTTCTCCTGAC[A/G]TCTCTTCCTGCCAGT | 83892 |
rs374342482 | snp | A/C | 0.000118873 | 0.00770858 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469479 | CTTGACCACATAACG[A/C]ATGGCCAGAGGCAGG | 83892 |
rs374533679 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475290 | ACCAGCCTGAGCAAC[A/G]TAAGACCTAATCTCC | 83892 |
rs374551839 | snp | A/G | 0.000135112 | 0.00821814 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469490 | AACGCATGGCCAGAG[A/G]CAGGCACATGGTGGG | 83892 |
rs374731416 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474111 | GTACAGACGGGATTT[C/T]TCCACATTGGTCAGG | 83892 |
rs374862342 | snp | A/C/G | 9.88572e-05 | 0.00702993 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457976 | AAGAAATTCCACAAG[A/C/G]GTGCCTCCAACATAC | 83892 |
rs374870805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462586 | TGCCTCCAGGGCCAG[C/T]AAGCACAATAAATGA | 83892 |
rs375045055 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469258 | GGTCCAGGGAAGATA[C/T]CTCTCTCTCCCCCAG | 83892 |
rs375383702 | snp | C/G/T | 6.65263e-05 | 0.00576709 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456334 | AAAGAGCATTTGATA[C/G/T]GGTGACCACAAGCTG | 83892 |
rs375625631 | snp | C/T | 0.000119088 | 0.00771556 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477289 | GGACGCAGGAGTCTC[C/T]AAACCCGGACTGAGA | 83892 |
rs375789423 | snp | C/T | 1.69473e-05 | 0.0029109 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451598 | TCTCTTGCCTGCTCA[C/T]TGGTGGAGGTGGGCC | 83892 |
rs375972261 | snp | A/G | 1.67273e-05 | 0.00289195 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451616 | GTGGAGGTGGGCCCG[A/G]TCATCAGGGCGCTTG | 83892 |
rs376023232 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468699 | GCTCTGTCGCCCAGG[A/C]TGGAGTGCAGTGGCG | 83892 |
rs376101923 | in-del | -/CAAA | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449013 | TTTGAAACAAACAAA[-/CAAA]AAAAACCCTTGATTA | 83892 |
rs376124450 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461113 | CCTTACACAAGGACA[C/T]CCAACAGGGGCCTCG | 83892 |
rs376175954 | snp | A/C/T | 5.1122e-05 | 0.00505557 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469469 | GGAAGCCCTCCTTGA[A/C/T]CACATAACGCATGGC | 83892 |
rs376205181 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468956 | TGTGCCCAGCCGATT[A/C]TTTGCCTTTTAATAA | 83892 |
rs376259551 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477250 | AGTCCATGGGCACCG[C/T]CCTCCCTACCATGAA | 83892 |
rs376416932 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461777 | AAGCCAGACAGATGA[C/G]AGGGTGAAGTCGAGG | 83892 |
rs376523703 | snp | A/G/T | 1.65315e-05 | 0.00287498 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469525 | CTTACCTTCACTGTC[A/G/T]GTGAGCACTTCCATG | 83892 |
rs376596938 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469557 | GCCCGCTGAACATGG[C/T]CTTCAGCATGGTGTC | 83892 |
rs376650363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468242 | GCCCCACACCCTGGC[C/T]TTCCCCAGGACACAG | 83892 |
rs376743176 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478586 | AGAAGTTCAAGACCA[A/G]CGTGGCCAACATGGT | 83892 |
rs376867378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452491 | CACATAAGCAGGTCC[A/C]ACACATTTGATCAGA | 83892 |
rs376895879 | snp | A/G | 0.000123523 | 0.00785789 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451562 | GCAGGGAGTGGGGGC[A/G]GTGAGAGGAGGGCGG | 83892 |
rs376897978 | in-del | -/CGTC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461987 | CTGTGCCCTGTTCCA[-/CGTC]CTCCTAACAATGCTG | 83892 |
rs377189484 | snp | C/T | 0.000365087 | 0.0135059 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451580 | GAGAGGAGGGCGGCT[C/T]GGTCTCTTGCCTGCT | 83892 |
rs377314709 | snp | C/G | 0.000131857 | 0.00811855 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460713 | GCAGCTCCTCGATCT[C/G]CCGGCGGCTCTCGGG | 83892 |
rs377353860 | snp | A/T | 0.000437904 | 0.0147905 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477331 | CACCCAGCTCACGCC[A/T]GCCGGGGGCGGAGGC | 83892 |
rs377602387 | snp | A/G/T | 6.756e-05 | 0.00581172 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456071 | GGAAGTTCTATAGGT[A/G/T]TGTGTTTCAGAACAG | 83892 |
rs386766302 | in-del | AACATCAACATCCAAG/CAAGTTC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466584 | GCTAACATCAACATC[AACATCAACATCCAAG/CAAGTTC]TTCTTGGTTTAGGAG | 83892 |
rs527236546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458907 | CACCCACAATGCAGC[C/T]CAGTGGACAACAAGG | 83892 |
rs527294276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465107 | CGCACAGAGAAACTC[C/T]CACGCACGGGGAAAG | 83892 |
rs527409743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471506 | TTAGCTCACCTGGGG[C/T]CTTTGCTGCCCGATG | 83892 |
rs527422624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464609 | TGGACCCCAAAGAAA[C/G]AGGATCCAGTATATG | 83892 |
rs527509450 | in-del | -/GAA | 0.00135013 | 0.025947 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457551 | CTCATCTGAAGGTAC[-/GAA]GAAGAAGAGCTGGGC | 83892 |
rs527570933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452921 | TTTTAGAGCTTAATA[A/G]GGAGCAAGGGGATTT | 83892 |
rs527756456 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451160 | AGGGAGCTCAGATAC[C/G]TCTGGTGGCCTCCAA | 83892 |
rs527830023 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450688 | AAGGAGGCTGAAGAG[A/G]AGCGGGATCCCAGGG | 83892 |
rs527867941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470625 | CCCCCACGGCTGGCC[C/T]TACCATTCCCATTGA | 83892 |
rs528020391 | snp | A/C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452997 | AGGTTCAGGAGTGGC[A/C/G]TGTTCTTGTGTTTGT | 83892 |
rs528233404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456999 | AGCCAAAAAGTGCAA[A/G]CAACCCAAATGTCCA | 83892 |
rs528240651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463778 | TTTCTCTTCTACAAA[C/T]GATCTCACAGGGTTG | 83892 |
rs528243900 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475038 | AAATGGAGTGTTAAA[A/G]CCATAATCTTCAAAA | 83892 |
rs528386144 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464112 | CCTTTCCCCTCTCCC[A/C]CCACCTCCAGGGAAC | 83892 |
rs528410889 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465562 | AGCCAAGCTTGAGAT[C/T]CACCTGGTGACCCCA | 83892 |
rs528522963 | in-del | -/TGAGAGGG | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461774 | AAGAAGCCAGACAGA[-/TGAGAGGG]TGAAGTCGAGGCCTT | 83892 |
rs528716589 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470391 | CTAGACTAGTGCTGC[C/T]CAAAAGAGCAAGATC | 83892 |
rs528771539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456066 | TGAAAGGAAGTTCTA[C/T]AGGTGTGTGTTTCAG | 83892 |
rs528832746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455713 | CCCAATTGCAGAGCC[C/T]CAAAAGGGCAGGCAA | 83892 |
rs528889504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469989 | CCCTAGAGAGGGCCA[A/T]GCATCCCCTAGTTTG | 83892 |
rs529038880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458296 | ATAGGCCAGGATGCT[A/G]AGTAAGTACTAACAA | 83892 |
rs529097016 | snp | C/T | 6.59663e-05 | 0.00574272 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457596 | TGGAGGTTTTCCTAG[C/T]AAATGGAGCTGTCTT | 83892 |
rs529119497 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464059 | CCCGCCCCGTGAGCA[C/T]ACCATGTGCTTCCTC | 83892 |
rs529309891 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455741 | CAAATTCAATTAAGG[C/G]GGGGCCAGATCTCTA | 83892 |
rs529375953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468777 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 83892 |
rs529418007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461905 | GCTTCAGTAGGAATC[A/G]GTCACTTTATGCTAC | 83892 |
rs529499112 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459195 | TCCTGAAGTTAGAAA[A/G]ACGAAGCAGAAATGA | 83892 |
rs529660008 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449694 | TGGTGCCACTACACT[A/C]CAGCCTGGCCAATAG | 83892 |
rs529787742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454541 | CGAGACCAGCCTGGG[A/C]AACATAGTGAAAGCC | 83892 |
rs529830645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468238 | TCCAGCCCCACACCC[G/T]GGCCTTCCCCAGGAC | 83892 |
rs529844613 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475097 | GGCACCTAGTCCTTT[A/C/G]TGTAGTTTCCTTTGG | 83892 |
rs529945062 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455171 | ACCTCAGTGTTTAGC[-/A]CTTCTTGGCTACCTT | 83892 |
rs530054897 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449171 | GCCCTTAGTGCTAAC[A/G]TAAGAAAAATCAGTT | 83892 |
rs530106211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473471 | GAAGTCTCAAACTAT[C/T]TTCTCTTTGGAAACT | 83892 |
rs530122641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472890 | TGCACATAATGAAGT[A/G]TACTTTAAGTGTACA | 83892 |
rs530162428 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467592 | GCCCTAGTGCACTTC[A/C]GCCTGGGTGACAGAG | 83892 |
rs530193000 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453911 | ATACTGCCCAGGACA[C/G]ACGGGCCACAGCATG | 83892 |
rs530332108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460501 | CCGAAGGAATCGGGC[A/T]CCAGGGCAAACTCAT | 83892 |
rs530525923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475143 | GGATCAGTGGTTCCC[A/T]ACCCTGGCTACTAGA | 83892 |
rs530527060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448863 | CTTGGGTCCTGAATC[A/G]CTGTTGTAAGGTACA | 83892 |
rs530578425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462544 | TGAGAAAACAAAATA[G/T]GGAATTAATATCTTA | 83892 |
rs530639529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468889 | GATCTCCTGACCTCG[C/T]GATCCGCCCGCCTCA | 83892 |
rs530746485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475589 | TCAGTCACTAGTGTT[C/T]AAAAAGCTCTTTGGG | 83892 |
rs530748097 | in-del | -/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448962 | GCCAGGAATTGTCTT[-/G]GACATGGGCCCCAGT | 83892 |
rs530832258 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474166 | GTGATCCATCTGCCT[C/T]GGCCTCCCAAAGTGC | 83892 |
rs530883823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467553 | CTTGAACCCAGGAGA[C/T]GGAGGCTGCCGTGAG | 83892 |
rs530980168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455676 | TGTATAATGTGAATT[A/G]AAAGTTTAAAAAGAC | 83892 |
rs531212106 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461587 | CACTGAGCTGACATT[C/T]CTCCACCAGAGATCC | 83892 |
rs531276571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460990 | CACAGCCTCCAGGCC[C/G]TACTGGCTGGACACA | 83892 |
rs531287223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452559 | GGAAAAATGGAGCAG[A/G]CACACTCTACCCCGT | 83892 |
rs531355725 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459705 | AAATTCTAGTTTCTA[C/T]AGTCATGCCAGTAGA | 83892 |
rs531604391 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478016 | AATGCTGGGTGATTT[G/T]TTCCTGTGGTTGTTG | 83892 |
rs531748920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465115 | GAAACTCCCACGCAC[A/G]GGGAAAGCGTTCAAG | 83892 |
rs531791202 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452824 | GGCAGAGAGGCTGGG[A/C]GGAAATCCTGGTTTT | 83892 |
rs531882060 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454213 | AGGTGACACAAGGTT[A/T]TGGAATTACCTGACA | 83892 |
rs531901669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467647 | AAAAGAATGCCCCAT[A/G]AAATGCCATACCATT | 83892 |
rs531916082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470759 | CAAAAACATAAACAT[C/T]ATCCAAAATACAAAA | 83892 |
rs532054721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453810 | GCAGCCTGTGAAGTT[C/G]TATATGAACTCCTAG | 83892 |
rs532065756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478583 | GTCAGAAGTTCAAGA[C/G]CAGCGTGGCCAACAT | 83892 |
rs532073863 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469616 | TAGTAGAGGGCTCCA[C/T]CCACATTCAGCTTCA | 83892 |
rs532115383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453320 | TCAGCCTCCCAAGTA[A/G]TTTAGACTACAGGCA | 83892 |
rs532324462 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474264 | ATTTCATTACCAATG[A/C]AGCTGGGGAGGTGAA | 83892 |
rs532400402 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471915 | GTAAAGTCAAAGCAC[A/C]GTAAATATGTGATAT | 83892 |
rs532499335 | snp | A/G | 1.68499e-05 | 0.00290253 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469494 | CATGGCCAGAGGCAG[A/G]CACATGGTGGGTGAG | 83892 |
rs532529492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459840 | CAAGGGTGAAGGAGA[A/G]TAGGAGGGGTATGGT | 83892 |
rs532560135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478729 | GAGGTTGCAGTGAGC[A/G]GAGTTCGCGCCGCTG | 83892 |
rs532582559 | in-del | -/TGAT | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449972 | TTTGACATTCAGTCA[-/TGAT]TGATTGTTTTAAAGT | 83892 |
rs532876173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472826 | AACTGTCATTATGTG[C/T]GCATGACTGTACCTT | 83892 |
rs532980666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463963 | GCCCCCAGGATGGAG[C/T]TGGTGTTGCTTTCAG | 83892 |
rs533049830 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476028 | ACCTATAAGAGCCCT[C/T]TGACTCCCAACTCCT | 83892 |
rs533084604 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477795 | GGCCGGTAGGGCCTG[A/C]GGTCCGGCCTGCGGG | 83892 |
rs533141080 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450626 | GGTATGGGCCACACT[A/G]AATTTCTAAGCAAAA | 83892 |
rs533232807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456981 | AACAGCATTACACAC[A/G]ATAGCCAAAAAGTGC | 83892 |
rs533247612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458774 | GGCAGCCGGCCAGGC[A/C]TAGACCCGTCAGGCA | 83892 |
rs533262757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459761 | AAAGAGCAGCACAGG[C/T]GAATTATGTGGAAAC | 83892 |
rs533359971 | snp | G/T | 1.6964e-05 | 0.00291233 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477271 | CTACCATGAAAAGTC[G/T]GAGGACGCAGGAGTC | 83892 |
rs533452700 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455194 | GCTACCTTAAGAACA[A/G]TATCTATTCTTTTAG | 83892 |
rs533508979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456508 | AGAGAAATTAGGTAA[C/T]TGCTCAAGGCTGAAC | 83892 |
rs533520593 | in-del | -/AAGTA | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448305 | GCATGGTCTGAGACT[-/AAGTA]AAGGAAATTTCCTAA | 83892 |
rs533684568 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451053 | ACATGGCAGAAAGCA[C/T]GTCTAGCAAAGCAGT | 83892 |
rs533712174 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457212 | ACATAAAAATGTCCA[C/G]AACAGGCAAATTCAT | 83892 |
rs533792780 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451293 | AAAAGTTCTCACATA[C/T]ACTTCACACTCATTC | 83892 |
rs533963259 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475259 | CGGGAGGATTGCTTG[A/C]GCCCAGGAATTCGAG | 83892 |
rs534020993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478166 | TAAATGGAGTAATTA[G/T]CAGGTTTCACAGAGG | 83892 |
rs534388630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457374 | TAGTCGTTATGGCCT[C/T]ACAACTTGTGAATAT | 83892 |
rs534472232 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449955 | ATCTGCCCAATACAC[A/G]ATTTTGACATTCAGT | 83892 |
rs534492784 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451515 | GAAGCAGAAGGGGCC[C/T]GGCAGCCTGCACAGG | 83892 |
rs534532115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456550 | CAGACACGCCCCCCA[A/G]AAGACAGCCCTGGCC | 83892 |
rs534794440 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452197 | TCTTGTGCCTAACTT[A/G]ACCTAGAGATCATTC | 83892 |
rs534943967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462640 | TGGGGCTGACAGGAC[A/T]GCATCTGCCCTGCCC | 83892 |
rs535042064 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454101 | GGAGTCCTTTAACAA[C/T]ATTCAAAATGTTTAG | 83892 |
rs535045224 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448528 | TACAGAAACATGACT[C/G]TCTTTTCCCTTCCAC | 83892 |
rs535063090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456647 | GGAGAGCACCTCACC[A/G]AGCCCCAAGAGGAGC | 83892 |
rs535105932 | snp | A/C | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449365 | GCTGCCAGAAACACT[A/C]GCTCATTAGGCATAG | 83892 |
rs535207100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474639 | CTTATTTAAGCTACC[A/G]TTAACTCCACGGTCT | 83892 |
rs535287182 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450733 | AGCTATGCCTGTCAC[A/G]GGGTCAGATGGCCTT | 83892 |
rs535392820 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450188 | CCATCCATCACCTGA[C/T]GCACATTCACATCTC | 83892 |
rs535568008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462219 | TATTCTTTGCATGAA[C/T]TGCCAGGAAAGTTTG | 83892 |
rs535576626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469078 | ATACTGACTATGTGC[C/T]GATGGCCCCACGGGG | 83892 |
rs535773155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457267 | TACCTAGGGCTGTGG[A/G]GTTGGGGAAGCAATG | 83892 |
rs535806594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478908 | AAACCTGGTGGCCCA[A/G]CTTTTCCTACTGCAC | 83892 |
rs535808756 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448962 | GCCAGGAATTGTCTT[A/G]GACATGGGCCCCAGT | 83892 |
rs536049811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468426 | AGCAGCACAGAAGAC[A/C]AGTCTCAGAAACAGG | 83892 |
rs536083910 | in-del | -/AAAC | 0.0849033 | 0.187731 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449005 | TGGCTTATTTGAAAC[-/AAAC]AAACAAACAAAAAAA | 83892 |
rs536109819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467194 | GGCAGCAAGTCCTGG[A/G]TTCAGCAGCTTCACC | 83892 |
rs536262245 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450283 | TTTGCAGGTGCAGAG[A/G]AGCCTGGGAGGTAGG | 83892 |
rs536316982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464896 | TCCTGCAATATCTAA[A/G]GAAGTAGAAGATGCT | 83892 |
rs536450398 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464496 | ACTGAGGTAGATCAA[C/G]GATGTAAGTGTAAAA | 83892 |
rs536535977 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458951 | AAACAGCTTTCAGAG[-/TC]TCTCATTCCTTCAAC | 83892 |
rs536581140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452655 | AAATCATGGCAGGCA[A/G]ATGGGGGAAACAACA | 83892 |
rs536641935 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459163 | GAAAGCAGGGCATTC[A/G]GACAGCAAGAAAAGG | 83892 |
rs536647900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467855 | TATGCTCTGTCCAGT[C/T]GGGGACAGGGGGACA | 83892 |
rs536658498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474531 | TGTAATTGGTCCGGG[A/C]TGTGGACTAGGCAAC | 83892 |
rs536800125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455772 | GCAGCACTATGCAGA[A/G]CAATCCAGCTTTGTG | 83892 |
rs536869204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462016 | TGTGCCCTGTTCCAC[A/G]TCCTCCTCAGACTGG | 83892 |
rs536984116 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461290 | TCTCACCCTCGCAGA[C/G]TGTGACCTCTGACTC | 83892 |
rs537201452 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448663 | AAACAGAAGCATTTT[A/T]TGACTTTTATTTTAC | 83892 |
rs537386282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453940 | TGGCACACAGCTAGG[A/T]CAGATTTGAAGGCTT | 83892 |
rs537540382 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474897 | TTCTCTGTAGAAGTC[G/T]TGTGTGCCTGTGTGT | 83892 |
rs537580213 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455394 | TTTCAATAATAAGTT[-/A]AAAAAAAAAAAGACT | 83892 |
rs538009994 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451314 | ACACTCATTCATACT[C/T]TTCCTCTGAGAACCG | 83892 |
rs538034840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465532 | GTACTGACCTCCTCA[A/G]GTGACTCCCTCTGTA | 83892 |
rs538052738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472224 | CATAGCTTAAAACAC[A/G]TATTGCACAGCTGTA | 83892 |
rs538068162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464729 | TAAAAACATGCTCAA[C/T]GTACCAGACATTAGG | 83892 |
rs538076655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458143 | ATTTTTAAAGTTGAC[C/T]GGCTGGACAGGCTCT | 83892 |
rs538216423 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472015 | TTGCTCTGGGTGAGC[A/G]AGTGGTGAGTAAATG | 83892 |
rs538245901 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477379 | TTCCGCTGTCCGCAC[C/G]CCACTTCCGCCCCGC | 83892 |
rs538285802 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479023 | TCCTGCCTCTTAGTT[A/G]TTACAGCCTTGACTC | 83892 |
rs538393039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458535 | AAGGTCACAGGTGAG[C/T]GTTAACCAAGGAGAG | 83892 |
rs538444339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467060 | AGCCCAGGCCTTCAC[A/G]AGGGCCCCCACCAGA | 83892 |
rs538458321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473668 | TTTTGGCAGCATTCG[C/T]GTCCTTGAGCCCAAG | 83892 |
rs538531251 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467947 | AGAGCCTCAGCTTTC[A/G]AGGCAACTCAGCAGC | 83892 |
rs538565275 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450110 | CGTTTTTGGAATACA[A/T]GTGTCAAAGGCTGCC | 83892 |
rs538799233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452573 | GGCACACTCTACCCC[A/G]TCTTCCTCACTGACA | 83892 |
rs538826002 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466442 | TCAGAGAAAAAGCCA[C/G]TTGTCCAATGTCACA | 83892 |
rs538827008 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466402 | AAAACATTATCATTC[A/C]TAACTGGGGAAGGAG | 83892 |
rs538870616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459114 | CAGTTGAGAGCAGAT[A/G]CGGCCTCCTAGGAAA | 83892 |
rs538871674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451930 | TTCTGCTGAAGGCCA[C/G]CAGTATTATTTTTAA | 83892 |
rs538890548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473118 | CCCATCAGGGTCAGT[C/T]ACTCTCAAGCTGGAG | 83892 |
rs539016568 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450782 | CAATCAGGAGAACAA[C/T]TGGACGGGGCTGGAG | 83892 |
rs539022233 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464816 | AGGTTGGACAGTGCC[A/C]AGGGTTGGCAAAAAT | 83892 |
rs539228752 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467897 | TTCTTTTTTGATATG[G/T]CATCAGGCCACCAAG | 83892 |
rs539265718 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459606 | GAATTTAACCAAAAC[-/T]GTGATGAACTGTACT | 83892 |
rs539369431 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468052 | GCTTCCTCCAGCAGC[-/G]GGGGTGCTATTGTCT | 83892 |
rs539392934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457742 | CAGATGCAATGAACT[A/G]CTAGCTTCCCATAGG | 83892 |
rs539577556 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463509 | AAGCAGCTCCTCGCA[C/T]GTGGGGGGTCTCTCT | 83892 |
rs539657390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469122 | TGCCCATTTCACCAG[A/G]GGAAGAAAATGAGAC | 83892 |
rs539727915 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478400 | ATTCAAAAGCATCCA[C/T]CTTAGATAGGCTGTA | 83892 |
rs539797388 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454671 | GAGTTCAAGGCTGCA[C/T]TGAGCTATGATTGTG | 83892 |
rs539805723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475334 | AAAAAAAAATTAACC[A/G]GTCATGGTGGCACAC | 83892 |
rs540026955 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453974 | AAATCAAACTGTCAC[C/T]GCAACTACAAACTAC | 83892 |
rs540036645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462980 | CTACCAGTTCTTTTT[C/T]GAGGGGAGCTCATTC | 83892 |
rs540097756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463808 | GACATAAAAATATGA[A/T]GAAAGAACGTACAGA | 83892 |
rs540243508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462326 | TCTCCACCCTCCAGC[A/G]GCTTCCACTTCCTAC | 83892 |
rs540283759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475443 | GATAATACCAGTGCA[C/T]TCTCCAGCCTGGGCG | 83892 |
rs540345161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475061 | CTTCAAAACCCTCAG[A/G]GAATGAATGTTAAAG | 83892 |
rs540488538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469904 | AATCTGGACTTCTGG[C/T]TTCTCCTAAAATCAG | 83892 |
rs540550055 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477206 | TATACTCTGCTGCTG[C/T]CCAGCTCCCTCGGCC | 83892 |
rs540634908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454385 | AACCTCAAACAAAAA[C/T]ACAACTTACCAGCAG | 83892 |
rs540735362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460885 | GCTGGGGTGTCTCTC[C/G]GCTCCCTCTACCTCC | 83892 |
rs540824674 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450340 | GCGCTGCGCCCAGCC[A/G]GGCTCCAGCAGGGGC | 83892 |
rs540888382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463205 | GCAGAACTCAGCTGC[C/T]TGGGAAGACCCAGGG | 83892 |
rs540899907 | snp | A/G | 0.00019769 | 0.00994012 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456148 | CTCAGTGGCATAGAC[A/G]ATGGAGGTACAACAG | 83892 |
rs540962884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448703 | ACGTTTGTACAACAT[A/G]CAGTGGCTACATCTA | 83892 |
rs541019326 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448176 | TATTTAGAAATTGGG[G/T]GATGTTTTTGTGCCC | 83892 |
rs541443384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448829 | CACGCTCCAGAGGGC[A/G]GGCTGAGTGTTGTTC | 83892 |
rs541589630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455473 | TCGAGGTCAGCTACA[A/G]AATCATGCAGAACTG | 83892 |
rs541610704 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468790 | CCCGAGTAGCTGGGA[C/T]TACAGGCACCCACCA | 83892 |
rs541666376 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473415 | CTAGCTCTGAGTAAA[C/T]ACTCCAAACACTCAA | 83892 |
rs542448514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467990 | CCTCCAGAGAGTGGG[A/T]AGGGTATGAGAAAAA | 83892 |
rs542603055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459564 | GCTTAACTGTCAGCC[A/G]TATTTACACGTCATG | 83892 |
rs542608692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452074 | GTTTCTCATCATTTT[A/G]CCCTCTCAAAGATTC | 83892 |
rs542614669 | snp | A/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448610 | GTAAACCGATTTTAG[A/G]GGCCTGGTTATGCCG | 83892 |
rs542615606 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465745 | TTTACCAAAGAGCAT[C/T]GTCATGGAAGGCAGA | 83892 |
rs542823924 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461652 | TGTCTCTGGGAGTGG[A/T]ATTTGTAGAAGACAG | 83892 |
rs542860050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478550 | CTTTGGGAGGCCGAG[A/G]CGGGCGGATCACCTG | 83892 |
rs543378511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454367 | ACAAATACAATAACC[A/G]ACAACCTCAAACAAA | 83892 |
rs543391911 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465110 | ACAGAGAAACTCCCA[C/T]GCACGGGGAAAGCGT | 83892 |
rs543394362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453745 | TGGCCGATCAGAGAA[G/T]GGGACTCCAGGGAAG | 83892 |
rs543577313 | in-del | -/AAAC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459079 | AAGGGAGAAGAAAGA[-/AAAC]AAACAGAATCATCAG | 83892 |
rs543639038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473350 | GCCCCAGCCCTACCA[C/T]TTAGTAGCTGTGTCC | 83892 |
rs543905240 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459028 | ATGAGAACAAAACCA[A/C]AACAAAGACAGGAAA | 83892 |
rs543970645 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450763 | TCCTGGAGTGGAGTC[A/G]GGTCAATCAGGAGAA | 83892 |
rs544001984 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455024 | GGGGTCTAATTACAG[A/G]AAGAATTCACAGCCC | 83892 |
rs544007800 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452104 | CTGTGCATGTAAATA[C/T]GTGTAATACACATAT | 83892 |
rs544053888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479246 | CCCTAACTAGATTGC[A/C]AGCTTCTTAAGGACA | 83892 |
rs544077882 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468579 | AAGGATGGAGCCCTG[C/T]TGTCAGGGGCTCTTT | 83892 |
rs544087496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458310 | TGAGTAAGTACTAAC[A/G]ATGATGACACATTTT | 83892 |
rs544196817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463602 | TCCCAGACCCATTAG[A/G]CAAGGCTGGAGAGCA | 83892 |
rs544270595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469328 | ATAAGCAAGCTAAGC[C/T]CTGGGTGAGGAAGTG | 83892 |
rs544393216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458755 | CCCCTTCCAGATCCC[C/G]AAAGGCAGCCGGCCA | 83892 |
rs544491649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471208 | TGGTAAAACACAAAC[C/G]TTATTTTTGTAAATG | 83892 |
rs544655263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478480 | TTTCCTATTCTTTAA[A/G]TAAAAATTAGATTAT | 83892 |
rs544716818 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477826 | AGAACTGGGTCGTCA[G/T]TCCTCCGAGTGGTGG | 83892 |
rs544729652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470615 | TCTGGGGTAGCCCCC[A/G]CGGCTGGCCCTACCA | 83892 |
rs544876854 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448368 | TAAATGGAACTCACA[C/T]GTGTCAAGGGATTGG | 83892 |
rs544879591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448862 | ACTTGGGTCCTGAAT[C/T]GCTGTTGTAAGGTAC | 83892 |
rs544990027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458179 | GGGGAGATGGGGCAG[A/T]CATGGCTGGGAAGAG | 83892 |
rs545012788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457548 | CATCCTCATCTGAAG[A/G]TACGAAGAAGAGCTG | 83892 |
rs545063377 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463767 | TGTCTAGCAGTTTTC[C/T]CTTCTACAAACGATC | 83892 |
rs545243007 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455597 | GACCGTCGGCCCACA[A/G]CAGACCTGCTGCATG | 83892 |
rs545599863 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472912 | AAGTGTACAGTTTGA[C/T]GTGTTTTGGTCAATA | 83892 |
rs545606500 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449430 | TTCTTCACACAAACA[C/T]TTAAAACACTATGCA | 83892 |
rs545720681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469376 | TAGCAAATCAACGAC[C/T]AAGTCAAGATGGTGG | 83892 |
rs545730841 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476289 | TTGCACAAAATGGAG[C/G]GGACTAGTCAACGTC | 83892 |
rs545796182 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450313 | GTCACTGAGAACACC[C/T]GTCCTACATAGGCGC | 83892 |
rs545940227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456765 | AGTTCCTGAGTTAGA[A/G]CCACATGTTTTCAAG | 83892 |
rs545954736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469828 | GTTTTGCTTGGGCCA[A/C]GCATACACAGCATTT | 83892 |
rs546020079 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477101 | CCAAAGCCCTTCCCC[C/G]ACCCCGGGCCTTTCC | 83892 |
rs546232243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474205 | CAGGCATGAACCACC[A/G]TGCCTGGCCAGGATC | 83892 |
rs546260735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462645 | CTGACAGGACAGCAT[C/G]TGCCCTGCCCCCAAG | 83892 |
rs546407295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456015 | ACAAGGCAAGCAAAG[C/T]ATTTTAAAAGCATTT | 83892 |
rs546431819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462264 | TCCAGGTTCCCCTGA[C/T]GAAACAGCTCAGCCT | 83892 |
rs546460561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457571 | AAGAGCTGGGCCTGG[A/C]TGGTGTGAGTGGAGG | 83892 |
rs546482799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461625 | TTTCAGAACTCCTCT[A/C]CTGAAATGCAGTGTC | 83892 |
rs546551755 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449597 | GGCATGGGCTGATGG[A/G]TACCTGCAATCCCAG | 83892 |
rs546608344 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471882 | AACAGACAAAAAAGT[A/G]CATAAAGTATACTTC | 83892 |
rs546664526 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476509 | CCCCACAGCTGAGAG[A/G]CAGATCTTGAAACAT | 83892 |
rs546677078 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475742 | TTAAGAAACACTGTA[C/T]TGAGGCTTGTATAAA | 83892 |
rs546779272 | snp | C/T | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457089 | AAAAGGAATGAAGTA[C/T]TGATTCATGCTACAA | 83892 |
rs546842558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463371 | CAAGGGAGCCAGGCA[C/T]ACTCTCCAGGAGGTT | 83892 |
rs547013927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461809 | CTTCTGACAAGCAGG[A/G]TGACCTCAGGCAAGG | 83892 |
rs547027397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468151 | AAGCTAAGTGTGAGA[C/T]GGCAGCTTTGGGGCT | 83892 |
rs547060883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453840 | GACCCACACCCAGCT[A/G]CAAGATCTACCCCTA | 83892 |
rs547061176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455092 | TGATGTCTTGCCAAT[A/G]TGGAGAGAGAGGCAG | 83892 |
rs547524613 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478266 | CTCCAGCTTAGCCCC[C/T]ACAGGCAATCTTGCA | 83892 |
rs547567673 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453331 | AGTAGTTTAGACTAC[A/C/G]GGCACACACCACCAT | 83892 |
rs547639374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459116 | GTTGAGAGCAGATAC[A/G]GCCTCCTAGGAAACA | 83892 |
rs547727265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466127 | CTCACTGCCACAGTG[C/T]CCTTGTCTTCTCAGA | 83892 |
rs547793178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472827 | ACTGTCATTATGTGC[A/G]CATGACTGTACCTTT | 83892 |
rs547828964 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459211 | ACGAAGCAGAAATGA[A/G]AATTTTGATAGAAGG | 83892 |
rs547903506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478732 | GTTGCAGTGAGCAGA[C/G]TTCGCGCCGCTGCAC | 83892 |
rs547909942 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448276 | CTTCCAAGAACCTAT[C/T]GATGACTTACTGTGC | 83892 |
rs547915522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478129 | GTTCCCTCACCTCTC[G/T]GAGCCTCAGTTTCCT | 83892 |
rs548028214 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468240 | CAGCCCCACACCCTG[A/G]CCTTCCCCAGGACAC | 83892 |
rs548067646 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461962 | GGCCAACATTTCCAC[G/T]CCTAACAACGCTGTG | 83892 |
rs548103180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474495 | ACTCCTGACACCTAG[A/G]TCCTACCATGAAAAT | 83892 |
rs548232812 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468369 | CCGCTTATGTGAAAA[C/T]TCACCCACCCTCCCA | 83892 |
rs548401881 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475065 | AAAACCCTCAGAGAA[C/T]GAATGTTAAAGCATT | 83892 |
rs548500815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453913 | ACTGCCCAGGACAGA[C/T]GGGCCACAGCATGGC | 83892 |
rs548571454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460502 | CGAAGGAATCGGGCT[C/T]CAGGGCAAACTCATT | 83892 |
rs548585180 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466897 | GAGCTGCAGGATGCA[A/G]GGAGTCTATCCCAGT | 83892 |
rs548664492 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472893 | ACATAATGAAGTATA[C/G]TTTAAGTGTACAGTT | 83892 |
rs548708772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458921 | CCCAGTGGACAACAA[A/G]GACCTTCCATGCACA | 83892 |
rs548754347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454675 | TCAAGGCTGCATTGA[A/G]CTATGATTGTGTCAC | 83892 |
rs548923153 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469743 | CCTGCCAGTGGAGAG[C/G]ATACAGGGTCATGAC | 83892 |
rs549032821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458502 | ACCAGTAAAAAAAGT[A/C]AAAAATTTGAGGGTA | 83892 |
rs549036190 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451170 | GATACCTCTGGTGGC[C/T]TCCAACTGCAGGACA | 83892 |
rs549285502 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477375 | TAACTTCCGCTGTCC[C/G]CACCCCACTTCCGCC | 83892 |
rs549317622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462613 | ATGAGTGCAGCTGGG[C/T]GGGGCTGAGGCTGGG | 83892 |
rs549426023 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478632 | CTAAAAATACAAAAA[G/T]TAGCCGGGCGTGGTG | 83892 |
rs549810143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452560 | GAAAAATGGAGCAGG[C/T]ACACTCTACCCCGTC | 83892 |
rs549949881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459027 | CATGAGAACAAAACC[A/G]AAACAAAGACAGGAA | 83892 |
rs549953561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460028 | TATGGGTACTGGTCC[A/G]GTGCGGGGCCAGACA | 83892 |
rs550010726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465177 | AACCCTCTACATGAT[A/C]ATCAACAGAATATGG | 83892 |
rs550012828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464730 | AAAAACATGCTCAAC[A/G]TACCAGACATTAGGA | 83892 |
rs550159423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471710 | TGAAGACCTCGAAGG[G/T]GGGGAGAAAAGGCTT | 83892 |
rs550176822 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478067 | GCCCCAGGACTCACC[C/T]AAACTGGAGTTCGAA | 83892 |
rs550464623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470788 | AAATGACCAAAGATC[A/C]CCTATCCTGGCTAAT | 83892 |
rs550644387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463431 | TGGTTGCTTTCAAAG[C/G]AGGAAGTGATCCCTT | 83892 |
rs550646260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470081 | GGGTGCCCCTAACTC[C/T]TGTGTTATAAGCACT | 83892 |
rs550674530 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476699 | CTGGGCTCTCTCGAT[G/T]TCTTTCCCTCACTGG | 83892 |
rs550762838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455742 | AAATTCAATTAAGGG[A/G]GGGCCAGATCTCTAG | 83892 |
rs550815206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457607 | CTAGTAAATGGAGCT[G/T]TCTTTCCCGGCTGAC | 83892 |
rs550954773 | snp | C/T | 3.84874e-05 | 0.0043866 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456385 | CTGGGCCCTTCTACA[C/T]GCAGGGCCCTACTGA | 83892 |
rs550996756 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449013 | TTTGAAACAAACAAA[C/G]AAAAAAAACCCTTGA | 83892 |
rs551073513 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451279 | TAAATATTGCAAACA[A/G]AAGTTCTCACATACA | 83892 |
rs551373638 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458430 | GACTGCAGAGGAATT[A/T]AAAAAAAAAGCATAA | 83892 |
rs551409484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463997 | CCCAAGGGAGGAGAA[A/G]GCTGCTCTGGGGGTC | 83892 |
rs551434564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456995 | CAATAGCCAAAAAGT[A/G]CAAACAACCCAAATG | 83892 |
rs551525512 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464115 | TTCCCCTCTCCCACC[A/T]CCTCCAGGGAACCTT | 83892 |
rs551556827 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449773 | TCCTGGCCAACATTC[A/C]CTTCGACTTTCTAAA | 83892 |
rs551590647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477321 | AGGCAGGAAACACCC[A/G]GCTCACGCCAGCCGG | 83892 |
rs551734650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452423 | CTGTTTGGCAAATCA[C/T]TGTGTTTGCTCATTG | 83892 |
rs551755773 | in-del | -/GATA | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472464 | AATCCCTTCTTCTGG[-/GATA]GATACCTCCAGAAGC | 83892 |
rs551890082 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478441 | AATAGTAGCTGTTAA[-/T]ATGAATAGTCTCTTT | 83892 |
rs551911678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475175 | TCACCTGCGTGTGCT[C/T]AAAAAACATGATGCC | 83892 |
rs552202030 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468263 | CAGGACACAGAGAGG[A/T]ATGTCCTCACCAGTG | 83892 |
rs552401476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468894 | CCTGACCTCGTGATC[C/T]GCCCGCCTCAGCTTC | 83892 |
rs552458676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475617 | GGGGGATTCGGATGT[A/G]GGACCAGGGCTTACT | 83892 |
rs552530442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453988 | CCGCAACTACAAACT[A/G]CAGAAGGCTGGTTAG | 83892 |
rs552570084 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455037 | AGGAAGAATTCACAG[A/C]CCTGAAAAAAAAAAA | 83892 |
rs552754654 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450011 | AGACTTTGCTGTTGG[A/G]TACAAAATGAAGGCA | 83892 |
rs552814900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467905 | TGATATGGCATCAGG[C/T]CACCAAGGCGAGGCC | 83892 |
rs552816162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456570 | CAGCCCTGGCCCCTA[A/G]GCCTGAGTGCTCCTA | 83892 |
rs552816253 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449289 | GGAATGTTTTATAAA[C/T]CTGTTCATATTCCAG | 83892 |
rs552977612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462208 | GCATAGTTTGGTATT[A/C]TTTGCATGAATTGCC | 83892 |
rs553048993 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468121 | CACAGCAAAGAGGAT[A/C]CTCCCACTCATAAAA | 83892 |
rs553122446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475245 | TTGGGAGGCTGAGGC[A/G]GGAGGATTGCTTGAG | 83892 |
rs553276268 | in-del | -/GC | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460933 | GCCTGGAGAATGGCA[-/GC]CTCACCTGCCTACCT | 83892 |
rs553385448 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448547 | TTTCCCTTCCACCTG[A/G]AGCGACTTTAAGGGG | 83892 |
rs553471459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454163 | CCAAGAAATTCTCAA[C/T]TCCTGTGGGAAATAA | 83892 |
rs553633955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474647 | AGCTACCATTAACTC[C/T]ACGGTCTTGGCCCAG | 83892 |
rs553649783 | in-del | -/CTGGAGAATGG | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460920 | GGAGAGCGGGACTGC[-/CTGGAGAATGG]CAGCCTCACCTGCCT | 83892 |
rs553671626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473217 | GTAGATTGAGAGCTA[C/T]GATACATAAGCTGAG | 83892 |
rs553914611 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460699 | CTTGGCTTCTGCTAG[C/T]AGCTCCTCGATCTCC | 83892 |
rs553966339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470908 | CAGAATTAGCCCTGC[C/T]TCCCAGCAGCATCCA | 83892 |
rs553977697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467118 | ACCATAAGGATGCCA[C/G]ACTCAAATGATCTGG | 83892 |
rs553989688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452620 | GGATGCACACAGCAG[C/G]TAACTGTGGACTCAG | 83892 |
rs553991206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453658 | ATCTTCATGCTCCTG[A/G]GCCCAAAATACAGGC | 83892 |
rs554002199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452038 | GTCTCCCTGCCCCTA[C/G]TTTCCCTTCTTAAAG | 83892 |
rs554051835 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454048 | TTGCCTGCTAAAACA[A/T]AAACATCAATGTTCT | 83892 |
rs554061562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458655 | CTGCAGTGGTTTGCA[A/C]GGTAGAGGACAGGGC | 83892 |
rs554178123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473856 | GCACGATCTCAGCTC[A/G]CCGCAACGTCTGCCT | 83892 |
rs554233405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464329 | AGATAATTCTTAGTT[A/G]TAAGAGGCTGCCCCG | 83892 |
rs554243104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473322 | AGGGTTTGGAGTTAG[A/G]CCTGTGCATAAGGCC | 83892 |
rs554262100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470493 | ACGCAGGCCTGGAAA[A/G]TGAGATTGGTATCCG | 83892 |
rs554467410 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472757 | GGCTACAGGAATTTT[G/T]CAGTTCCATTATAAT | 83892 |
rs554712642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459179 | GACAGCAAGAAAAGG[C/G]TCCTGAAGTTAGAAA | 83892 |
rs554726204 | snp | G/T | 0 | 0 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455266 | TCATCCTGTGAGTGC[G/T]GGGGAGGAGGAGTAG | 83892 |
rs554761003 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464167 | CTAAGGTATTTATAC[C/T]CTATATTTTTGTGGT | 83892 |
rs555068484 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464908 | TAAGGAAGTAGAAGA[A/T]GCTGTCCCAATTCCC | 83892 |
rs555209869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453383 | TTTTTGGTAGAGACA[C/G]GGGTGTTGCTATGTT | 83892 |
rs555233072 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448170 | GGTCTTTATTTAGAA[A/C]TTGGGTGATGTTTTT | 83892 |
rs555322490 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450130 | CAAAGGCTGCCCATG[C/T]TAATACCTTTGGTAT | 83892 |
rs555372385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478167 | AAATGGAGTAATTAG[C/T]AGGTTTCACAGAGGG | 83892 |
rs555374433 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477029 | CCCAAATGTGCTTCC[C/T]GGATTCCTAACCGCC | 83892 |
rs555376848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469210 | AACCCAGGTTGGCAA[C/G]TCTTTGTCAAGACCC | 83892 |
rs555637046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471067 | TTGACTACAGGTATG[C/T]TCCTCGTGCTTTTTG | 83892 |
rs555660362 | snp | C/T | 0.000197681 | 0.00993988 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458004 | TACCTTATTTGAAGT[C/T]GCTATAAGTTTTTGT | 83892 |
rs555661626 | snp | A/G | 0.000131833 | 0.00811782 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469652 | TTGGAGCTGGGGCTC[A/G]TGCCCTTGAAGGAAG | 83892 |
rs555729262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464090 | TCTCCCTGGATGTCT[A/G]ACCTCTCCTTTCCCC | 83892 |
rs555793619 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458361 | CAAAAATAAACCCTT[A/G]ACGTGGCAGCAGAAA | 83892 |
rs555968306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457375 | AGTCGTTATGGCCTC[A/G]CAACTTGTGAATATA | 83892 |
rs556166667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470362 | GGAACCAAGTTATTG[A/C]AAAATTAGACCTCCT | 83892 |
rs556172552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472227 | AGCTTAAAACACATA[C/T]TGCACAGCTGTACAA | 83892 |
rs556184657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478985 | TCAGCTTTGGAAATA[C/T]AGAGGTAAGACAAGA | 83892 |
rs556372581 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477431 | TCCGTTGTGCGCCTA[A/G]GGGCCAGTTTTCTTT | 83892 |
rs556377679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458536 | AGGTCACAGGTGAGC[A/G]TTAACCAAGGAGAGG | 83892 |
rs556420096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465543 | CTCAGGTGACTCCCT[C/T]TGTAGCCAAGCTTGA | 83892 |
rs556619380 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477083 | CCGCCCCTAATTCTC[C/T]ACCCAAAGCCCTTCC | 83892 |
rs556743319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455974 | TTGCAGGGCCTAAAA[A/G]ATAAATATTTTAAGG | 83892 |
rs556766593 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451328 | TTTTCCTCTGAGAAC[C/T]GAGAAAGCCTGGCTC | 83892 |
rs556768456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458144 | TTTTTAAAGTTGACC[A/G]GCTGGACAGGCTCTG | 83892 |
rs557030537 | in-del | -/CA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468075 | TATTGTCTTGATTTC[-/CA]CAGATACTCTCGGGC | 83892 |
rs557055546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462950 | GACAAGGCAGGGAAA[A/G]ACCGTATTATCTTTC | 83892 |
rs557105949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462227 | GCATGAATTGCCAGG[A/G]AAGTTTGATAACAGG | 83892 |
rs557116337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469081 | CTGACTATGTGCCGA[C/T]GGCCCCACGGGGGAG | 83892 |
rs557280117 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450165 | CGGTAACGATTCCCT[C/T]GACAAACCCATCCAT | 83892 |
rs557392296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461727 | TGGAGCAAAGTCCAA[A/G]TATCTCCCAACAGCA | 83892 |
rs557494830 | in-del | -/A | 0.00111649 | 0.0236008 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464863 | AGTAGAAGTTGCCAT[-/A]ACCACTCCAGAAGGG | 83892 |
rs557527430 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450322 | AACACCCGTCCTACA[G/T]AGGCGCTGCGCCCAG | 83892 |
rs557614049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468430 | GCACAGAAGACCAGT[C/T]TCAGAAACAGGAAGG | 83892 |
rs557623404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475317 | CTCCACAAAAAAATT[A/G]AAAAAAAAAATTAAC | 83892 |
rs557664672 | in-del | -/A | 0.161267 | 0.233723 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472511 | TTACAGTTTTCACTT[-/A]AAAAAAAAAAAGGCA | 83892 |
rs557834065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475379 | CTACTCGGGAGACTG[C/T]GGTGGGAGGACTGCT | 83892 |
rs557908049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456869 | AGTTTGGCAGGTCCT[C/T]GAATGATTAAACATA | 83892 |
rs558002727 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454319 | GGAGTCTCAGCAAGG[A/G]GACAGAAAAACCAAA | 83892 |