SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs966058 | snp | C/G | 0.499996 | 0.00139776 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579919 | TCTGGGAATTAGTTT[C/G]AGAAGTTTAACAATG | 7347 |
rs966059 | snp | C/T | 0.493013 | 0.058691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580214 | GACTTCTTTGCCAAC[C/T]GAACATGGATACTCT | 7347 |
rs972542 | snp | C/G | 0.495135 | 0.0490805 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587064 | ccaaaatgcataaaa[C/G]gtagaaataacaaag | 7347 |
rs973122 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552101 | GTATATGATTGTACA[C/T]TATATCTGGCATGCT | 7347 |
rs974373 | snp | A/G | 0.402982 | 0.197728 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589660 | TTTAGTGGCTTTTAC[A/G]TATTAATTTCCATGA | 7347 |
rs975937 | snp | C/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550756 | CTCAACAGCTCATTT[C/T]TTTTTTACTGCTCTT | 7347 |
rs975938 | snp | A/G | 0.499989 | 0.00239614 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551056 | ttatgaatctatgtt[A/G]acttttcgcaaatga | 7347 |
rs975939 | snp | A/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551081 | aaatgatttttctgc[A/T]tctcttgagatgatc | 7347 |
rs1323696 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556625 | ATGAGGAAGAATTTG[C/T]TATAATTTAGGGACA | 7347 |
rs2031234 | snp | A/G | 0.093777 | 0.195178 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566361 | CCATTGATGTCTTAG[A/G]CCAATCTCCTACAAA | 7347 |
rs2031235 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566498 | AATGCCTTTTTCCCC[A/G]TACCTTCACCTTCAC | 7347 |
rs2031236 | snp | A/G | 0.316485 | 0.240998 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595641 | aaGAGCGTAATAGTT[A/G]TAATGATTGGGCTGA | 7347 |
rs2181672 | snp | G/T | 0.364193 | 0.222396 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563127 | GTACCTCATTATCCT[G/T]TATGTATGTATGTAT | 7347 |
rs2274046 | snp | G/T | 0.225597 | 0.248806 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595083 | GATATTTATTGTGTT[G/T]ACTTAAATTAACTGG | 7347 |
rs2274047 | snp | C/G | 0.225301 | 0.248777 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595211 | ATGTTTGCATACCAT[C/G]TTCGCATTTTAGCAA | 7347 |
rs2274048 | snp | G/T | 0.225893 | 0.248835 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605906 | GATATTTTCATTAAC[G/T]TGATGATTAAACTTT | 7347 |
rs2281762 | snp | A/G | 0.484209 | 0.0874434 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549542 | GTCCAAGCGTGAGGG[A/G]AGAGGGCTGTGGATT | 7347 |
rs2296146 | snp | C/T | 0.287663 | 0.247154 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569436 | AGGCATTTTTTCCAA[C/T]GAATACCTTTATTCT | 7347 |
rs2328959 | snp | A/G | 0.411914 | 0.190483 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602065 | AGACTATACAGAAAc[A/G]caatctcagctcact | 7347 |
rs2328960 | snp | A/C | 0.411914 | 0.190483 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601867 | CCACCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 7347 |
rs2328961 | snp | A/T | 0.488545 | 0.074807 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601809 | GAAATAAAAACTTTT[A/T]AAAAATGTACAGGCT | 7347 |
rs2328962 | snp | C/T | 0.493432 | 0.0569306 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601729 | catgcctgagagata[C/T]tgtgggttagcttcc | 7347 |
rs2328963 | snp | A/G | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601390 | TAAGACAATAATGAA[A/G]TTTGCCACATTTGAC | 7347 |
rs2328964 | snp | A/C | 0.397994 | 0.201489 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564694 | caaaTGATAACAACA[A/C]AACACTATCATTGat | 7347 |
rs3036429 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587017 | ttttttttttttttt[-/T/TT/TTT]gctaccttaaggtaa | 7347 |
rs3783028 | snp | A/G | 0.411746 | 0.190626 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591146 | GAAAGAATGCTTGCC[A/G]TTGACTTTTAATTGT | 7347 |
rs3812844 | snp | A/G | 0.483995 | 0.0880135 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549320 | GCCGTGCAGCACGGT[A/G]CTGTTGTTCGTTTGT | 7347 |
rs3812845 | snp | C/G | 0.499997 | 0.00119808 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549310 | ACGGTGCTGTTGTTC[C/G]TTTGTCGGGGTGCAG | 7347 |
rs3812846 | snp | A/G | 0.499998 | 0.000998401 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549162 | AGTTGAGTTCACTGT[A/G]GAGTAGAGGCAGTGG | 7347 |
rs4325432 | snp | C/T | 0.365232 | 0.22186 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561838 | ATACGTACGTATATA[C/T]GTATACGTATACATA | 7347 |
rs4539477 | snp | C/T | 0.486332 | 0.08153 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579279 | AATACATGTATCATG[C/T]GGTTCAAGATGTAGA | 7347 |
rs4611344 | snp | A/G | 0.412416 | 0.190055 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601192 | tactcctaataaaga[A/G]gtcatgaacagtgtt | 7347 |
rs4632012 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598498 | catgtttctttgtct[C/T]ctttaatctggaaca | 7347 |
rs4884008 | snp | A/T | 0.475148 | 0.108842 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560892 | AAAAGGTAATTGTTA[A/T]GTAAAATAGAAAGTT | 7347 |
rs4884009 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564250 | ccgcctcctgggttc[A/G]cgccattctcccacc | 7347 |
rs4885310 | snp | A/C | 0.0952156 | 0.196321 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549649 | CACTTGACCTACGGC[A/C]CTGCACGGAGCGGTT | 7347 |
rs4885311 | snp | G/T | 0.100588 | 0.200439 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558707 | CATACAGATGGCTAG[G/T]TTATCTACTAAAGTA | 7347 |
rs4885312 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563908 | tcccttttttaaagc[C/T]gaataatatttctgt | 7347 |
rs4885313 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564173 | tttttttttttgaga[C/T]ggagtctcgctctgt | 7347 |
rs4885314 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564236 | gctcactgcaagctc[C/T]gcctcctgggttcgc | 7347 |
rs4885315 | snp | C/T | 0.102014 | 0.201495 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564318 | accacgcccggctta[C/T]tttttgtatttttag | 7347 |
rs4885316 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576530 | cagctaattttttgt[A/G]tttttagtagagaca | 7347 |
rs4885318 | snp | A/G | 0.397452 | 0.201886 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577401 | tacaagtaatctaga[A/G]atgatttaaagtata | 7347 |
rs4885319 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584968 | ccacacaaaacaaac[A/G]gtgcatccaacagct | 7347 |
rs4885320 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586264 | gaaatattcccagtg[A/T]tgaagaaggacatta | 7347 |
rs4885321 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586880 | tgcaggggttggaga[G/T]aaatctatagcatga | 7347 |
rs4885322 | snp | A/G | 0.411914 | 0.190483 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597195 | AGTGAGTAGAAAATA[A/G]TGATTAAGAGATTAG | 7347 |
rs4885323 | snp | C/T | 0.411746 | 0.190626 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598278 | ttgaagacatgatgc[C/T]ccattatctttaaaa | 7347 |
rs4885324 | snp | A/G | 0.39121 | 0.2063 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599611 | tttgatattactacc[A/G]taattgttttgggat | 7347 |
rs5804819 | in-del | -/AGT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552034 | TGTAATACATGGAAT[-/AGT]GACAGGAGACCTTTC | 7347 |
rs5804820 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563044 | TTTGTCTTTGAAGTT[-/C]CAATTTAGAAATTGA | 7347 |
rs6145127 | in-del | -/TGTCT/TGTCTTGTCT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571976 | AAGTTTTCCTAACCC[-/TGTCT/TGTCTTGTCT]TGTCTTGTCTTGTCT | 7347 |
rs6562910 | snp | G/T | 0.100588 | 0.200439 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576269 | aagtctcgctctgtc[G/T]cccaggctggagtgt | 7347 |
rs6562911 | snp | A/G | 0.100588 | 0.200439 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576405 | cggctaattttttgt[A/G]tttttagtagagaca | 7347 |
rs6562912 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576795 | ATGTGTAGCCCTAAA[C/T]GAAATACGGTTGAAT | 7347 |
rs6562913 | snp | A/T | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593297 | CTTAAAAAATTGGAC[A/T]CTCTTCTGATTATTG | 7347 |
rs6562914 | snp | A/C | 0.423905 | 0.193944 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593401 | TTATCACTGTCTTCA[A/C]ATATTTAAAGAAATA | 7347 |
rs6562915 | snp | G/T | 0.411914 | 0.190483 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596750 | GTTTTACTAGTTAGA[G/T]AGCTGTCTTGGCTCA | 7347 |
rs6562916 | snp | A/G | 0.411914 | 0.190483 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597086 | ACATTACAAAGATGG[A/G]CAGTTGCTGATTCAT | 7347 |
rs6562918 | snp | C/T | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600441 | tcttgttaatgcaga[C/T]ggtgactttcagttg | 7347 |
rs6650448 | snp | A/G | 0.103438 | 0.202533 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581401 | gttgctcaggcggca[A/G]tgcagtgggtcgatc | 7347 |
rs7139740 | snp | C/T | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592806 | AGATTAAAGGTGCAA[C/T]GATGCACAATTTTGA | 7347 |
rs7139862 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570097 | TGACTGTATCACTCT[A/G]AGAGGAAGTTTGTCA | 7347 |
rs7317172 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593158 | TAGAGTATTTCATAT[C/T]CTGTTGGAAAATTGT | 7347 |
rs7317250 | snp | A/G | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593005 | AGTTCTCTGACTCCA[A/G]TTGTACTACTTTTAC | 7347 |
rs7317893 | snp | G/T | 0.499946 | 0.00519141 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578918 | TGTTTAGAATCTACT[G/T]GGCTTTTTTGGCCCA | 7347 |
rs7319441 | snp | A/G | 0.499999 | 0.000599041 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558348 | AGCTTTGGCTGACAT[A/G]GAGTAGATTTGCAGT | 7347 |
rs7321611 | snp | C/T | 0.102014 | 0.201495 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606352 | GTGTTAGGGAATGAC[C/T]GAGCAGCTACTTTAG | 7347 |
rs7324560 | snp | A/G | 0.101658 | 0.201233 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588744 | CCTTAAGAGAAATCT[A/G]TTATGGTTGTTACGG | 7347 |
rs7326807 | snp | A/G | 0.499961 | 0.0043928 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548766 | GTGAAGAAGAAAAAA[A/G]AGACACTGCTACTGG | 7347 |
rs7330411 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595098 | TACTTAAATTAACTG[A/G]TTGCCTATAAAATTG | 7347 |
rs7331205 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574075 | acaaaaaaactagcc[A/G]ggtgtggtggcgggt | 7347 |
rs7337186 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565499 | TACTTGTAGGTTTTC[C/T]ATAGACATCGTTTGT | 7347 |
rs7339146 | snp | A/G | 0.376791 | 0.215463 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599583 | tctgttatggtatct[A/G]tgatcagtgatcttt | 7347 |
rs7358977 | snp | C/T | 0.499996 | 0.00139776 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566163 | TATTAAGTTTTTGCA[C/T]ACCCTTTCAGACTTT | 7347 |
rs7982517 | snp | A/G | 0.409552 | 0.192466 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587903 | ttcccccagctcagt[A/G]ttcctctcttgtaac | 7347 |
rs7982534 | snp | A/G | 0.487049 | 0.0794222 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557849 | GATTCACACCACCCA[A/G]GCTAACTGCTAACAT | 7347 |
rs7982613 | snp | A/G | 0.499974 | 0.00359416 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596377 | AAGATGTGCCTTGCT[A/G]ATTGAGTCTACAAAA | 7347 |
rs7984443 | snp | C/T | 0.488606 | 0.0746142 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597361 | GGTGACATGGCAAGA[C/T]GTCATCTCTTAAAAA | 7347 |
rs7985066 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576038 | attacaggtgtgagc[C/T]accgccccagccAAA | 7347 |
rs7985714 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570479 | ctgaccttgtgatcc[A/G]cctgtctcagcctcc | 7347 |
rs7987763 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570817 | CTAGGGAGGCTGAGG[C/T]GGGAGGATTACTTGA | 7347 |
rs7989568 | snp | C/T | 0.397813 | 0.201621 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581428 | GATCTTGGCTCCCTG[C/T]AGCCTTGATCTCCTG | 7347 |
rs7989619 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567825 | AGTGCTGGGATTACA[A/G]ACATGAGCCACCGTG | 7347 |
rs7991577 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577245 | acagagaccttgtct[C/T]agacaaaaaagagaa | 7347 |
rs7995889 | snp | C/T | 0.484209 | 0.0874434 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549505 | TAGAACGCGAGCGCT[C/T]GGCAAGGCTCGGCTC | 7347 |
rs7995945 | snp | A/G | 0.10237 | 0.201756 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591466 | TGTAAATTCTGACAT[A/G]AGCACAATTGATCCA | 7347 |
rs7996485 | snp | C/T | 0.0291538 | 0.117162 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549811 | AGCTGGAGGGCCGGG[C/T]ACCGCGGCCATGGAG | 7347 |
rs7996527 | snp | A/T | 0.103794 | 0.20279 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574291 | ttctgtatttttttt[A/T]atgataaaatcctgt | 7347 |
rs7996884 | snp | A/T | 0.411914 | 0.190483 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598608 | ctccaatttaggcca[A/T]ctgatttatcctcat | 7347 |
rs7996897 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561819 | TATACATACGTATAC[A/G]TATATACGTACGTAT | 7347 |
rs7996903 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561827 | CGTATACGTATATAC[A/G]TACGTATATACGTAT | 7347 |
rs7997046 | snp | A/G | 0.221737 | 0.248397 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561881 | TACATACGTATATAC[A/G]TATACATATATACAC | 7347 |
rs7997260 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592084 | AGTGCCTGGTGGTAT[A/G]TATTAAGTGCTATAC | 7347 |
rs7997463 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562118 | CTTCAGGACTAAATG[A/G]AGCCAAATCCCACAG | 7347 |
rs7998005 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556467 | AATAAATTAGTAACA[A/G]GGCAGAATCTCTGGC | 7347 |
rs8000062 | snp | A/G | 0.499974 | 0.00359416 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596332 | AGTCATTATTTTGGT[A/G]GTATATAATGGACCT | 7347 |
rs8000362 | snp | A/G | 0.142272 | 0.225598 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596264 | TGTGCAACCCTGAGC[A/G]TTGTCTACAATACTA | 7347 |
rs8001271 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553669 | gttctaataccatca[A/G]ttgtcacatagatga | 7347 |
rs8001729 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592430 | Catatatatatatat[A/G]tatatatatatatat | 7347 |
rs8192737 | in-del | -/GGCGAAGGCGGCGGC | 0.389018 | 0.207783 | intron-variant, upstream-variant-2KB, cds-indel | UCHL3, COMMD6 | GRCh38.p7 | 13:75549775 | GGAAGCGGCGGCGGC[-/GGCGAAGGCGGCGGC]TGTCAGAGCTGGAGG | 7347 |
rs8192738 | snp | C/T | 0.499462 | 0.0163966 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550015 | TCTGTCGCTCGGGAC[C/T]TCGGAGTCTTTTCTG | 7347 |
rs8192739 | in-del | -/ATA | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555626 | TTTATTATAATAATA[-/ATA]TATAAGTAGAAGAAT | 7347 |
rs8192740 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558104 | CTCATGGCAATCTGG[A/C]GTCAGGATCTAACAA | 7347 |
rs8192741 | snp | C/T | 0.499996 | 0.00139776 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559787 | TATAGTGATGCATTT[C/T]TAATATGATTTTTGT | 7347 |
rs8192742 | microsatellite | (T)9/10 | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560725 | ACTAATGTTCCATTG[(T)9/10]CTTTCTTTCTTTTAC | 7347 |
rs8192743 | microsatellite | (TA)6/7 | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561543 | ATACAGTTTTTTCAA[(TA)6/7]AGGAATCTTCTTTGC | 7347 |
rs8192744 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561747 | TCTACATATTTTAGT[C/T]TTTTTTTCTAGAATG | 7347 |
rs8192746 | snp | C/T | 0.494936 | 0.050064 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565933 | GTCAGCTATAGAGCC[C/T]ACATTTTTGATGCTT | 7347 |
rs8192747 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571698 | AGGGGTTTCCTAGTG[C/T]GTAGAGCAGTGATTC | 7347 |
rs8192748 | snp | C/G | 0.499958 | 0.00459246 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577771 | AAGTCAAATGTGAAG[C/G]CAAGAAAGAAAAATC | 7347 |
rs8192749 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578248 | AGTAAACCACAATTT[-/A]TTTTTCATTTCCTTA | 7347 |
rs8192750 | snp | A/T | 0.486398 | 0.0813386 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578966 | GTGGCAGTAAATAGT[A/T]TAAAGTTTCATCTTC | 7347 |
rs8192751 | snp | C/T | 0.488485 | 0.0749998 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579665 | TTAAAGGAAAATTCT[C/T]AGACCGAACTTACCA | 7347 |
rs8192752 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580346 | TAAAAAATCTACAGA[A/C]ATCCATTTAGAATTA | 7347 |
rs8192753 | snp | A/G | 0.486332 | 0.08153 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582000 | AATTAGTTGACAGTT[A/G]ATGGGCGAGTGACCT | 7347 |
rs8192754 | in-del | -/CCT | | | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75589942 | TAATTATGTAGTCCT[-/CCT]CGCCATCCTCATCAC | 7347 |
rs8192755 | snp | C/T | 0.451109 | 0.148509 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590709 | CTGATCTTTCCTGCC[C/T]ATTCAGTTTCTAAAG | 7347 |
rs8192756 | snp | C/T | 0.411746 | 0.190626 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590802 | TTATGATTTCTCTTT[C/T]ATAGGCTAATGATAT | 7347 |
rs8192757 | snp | A/G | 0.258565 | 0.249853 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591285 | TTCTGCTGAGTATCA[A/G]CAAACTCACATCTCT | 7347 |
rs8192758 | in-del | -/TGTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594236 | TAATTTCAAATTGTT[-/TGTT]AAGCATCAAAGCAAG | 7347 |
rs8192759 | snp | C/T | 0.5 | 0.00019968 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594591 | ATTCATTTCATTCAG[C/T]AAGTATGCAATGTGC | 7347 |
rs8192761 | snp | G/T | 0.225893 | 0.248835 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597863 | GTATTAATTCCCTAC[G/T]CTAATAAATTGTAAG | 7347 |
rs8192762 | snp | A/T | 0.391583 | 0.206044 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602544 | GAGCCTCATGGATTC[A/T]TCTGCAGCGTATGCA | 7347 |
rs8192763 | snp | A/T | 0.391397 | 0.206172 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605034 | TGAACAAATGTAAAA[A/T]TTGAAAAGGCAAGAA | 7347 |
rs8192764 | snp | C/G | 0.411914 | 0.190483 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605079 | TTGCTCATTATATCC[C/G]AGATTTCATCAAATC | 7347 |
rs8192765 | microsatellite | (T)9/10 | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605710 | ACTGAAAAATCATAC[(T)9/10]CCTCCATAGGATGCC | 7347 |
rs9318357 | snp | A/T | 0.499946 | 0.00519141 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575044 | GTAATAACAAGTAGC[A/T]TCATCACTGGCATCA | 7347 |
rs9318358 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575295 | TGAACAGTAGCCCCA[C/T]CTCACTTATGCTTCA | 7347 |
rs9318359 | snp | G/T | 0.216048 | 0.247684 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592266 | GATTGGAAGTCAATG[G/T]TACTATTTATACTAA | 7347 |
rs9318360 | snp | C/T | 0.225301 | 0.248777 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596031 | TTTTGGTTCTATTAC[C/T]TCTCATTTGCTGTCT | 7347 |
rs9318361 | snp | A/G | 0.411914 | 0.190483 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602944 | TAAACAGCTGCATTC[A/G]AAGGAAAATTGCTCA | 7347 |
rs9530447 | snp | A/G | 0.39121 | 0.2063 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592666 | GCTGACTGAAGGAAA[A/G]GGCTTATCACAGGTT | 7347 |
rs9543972 | snp | C/T | 0.393434 | 0.20476 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547539 | CCCAATCTTGGGCTC[C/T]GTCTCAGACTTATTG | 7347 |
rs9543973 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554756 | ACTTGAAACTTTTtt[G/T]tttttttaaactttt | 7347 |
rs9543974 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554757 | CTTGAAACTTTTttg[G/T]ttttttaaactttta | 7347 |
rs9543975 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559283 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 7347 |
rs9543976 | snp | A/G | 0.456095 | 0.141508 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562512 | TATTCCAGGACCCCA[A/G]TTGTAATGAACAGTA | 7347 |
rs9543977 | snp | A/G | 0.171057 | 0.237209 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562840 | AGTAGAAAATGATGT[A/G]AGTAAATATATAAGT | 7347 |
rs9543978 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563167 | tatgtatgtatgtat[A/G]tatatgtttatgtTT | 7347 |
rs9543979 | snp | G/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564814 | gattctcatggctca[G/T]tctctggagtagctg | 7347 |
rs9543980 | snp | C/T | 0.499942 | 0.00539106 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570766 | GTAATAAAAATTAGC[C/T]AGGTGTGGTGGTGCA | 7347 |
rs9543982 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577983 | CCATGTAAATTAATA[A/G]TAATAATGAAAAATA | 7347 |
rs9543983 | snp | A/G | 0.211212 | 0.246973 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579612 | TTCTTTTCTGATCTC[A/G]GAATTTTAGAAATGG | 7347 |
rs9543984 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581546 | TTTTTTTTAGTAGGG[G/T]GGGGTCTCCCTATGT | 7347 |
rs9543986 | snp | A/G | 0.225597 | 0.248806 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587638 | tggaagtaaaatgtc[A/G]tagtcaaatctgggt | 7347 |
rs9543987 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592423 | TTTCCTTCatatata[C/T]atatatatatatata | 7347 |
rs9543988 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592438 | tatatatatatatat[A/G]tatatatatatatat | 7347 |
rs9543989 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592446 | TATATATATATATAT[A/G]TATATATATATATAT | 7347 |
rs9543990 | snp | G/T | 0.420574 | 0.193168 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598298 | tatctttaaaacttc[G/T]gtgtgtattttctca | 7347 |
rs9543991 | snp | C/T | 0.258565 | 0.249853 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600870 | atagtaaattggaaa[C/T]ttcctggaaaggatt | 7347 |
rs9543992 | snp | A/G | 0.39121 | 0.2063 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600938 | tgggaagagctcaaa[A/G]tatcaacattaacat | 7347 |
rs9543994 | snp | A/G | 0.499974 | 0.00359416 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602763 | GGAGGCATTAAAAAT[A/G]CACTGAGGGCTGGAT | 7347 |
rs9543995 | snp | A/G | 0.224412 | 0.248687 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603579 | TGCCTTTATGTAAAC[A/G]TTAAAAAATAATACA | 7347 |
rs9543996 | snp | C/T | 0.487933 | 0.0767327 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606242 | gaaaaatgtgatagt[C/T]atggagcttatgtta | 7347 |
rs9543997 | snp | A/G | 0.490119 | 0.0695896 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606337 | attaaaataggattt[A/G]tgttagggaatgacc | 7347 |
rs9565175 | snp | C/G | 0.488545 | 0.074807 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575854 | CCTCCCTGGTTCAAG[C/G]GATTCCCCTGCCTCA | 7347 |
rs9565176 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586050 | TAAAGACTCaaatgt[C/T]tataaaccctcaaat | 7347 |
rs9573583 | snp | G/T | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547944 | ctaccaatttgagtg[G/T]atccctagcaagaca | 7347 |
rs9573584 | snp | A/C | 0.499998 | 0.000998401 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554173 | gctcaagcactcctc[A/C]cacctcagccttcca | 7347 |
rs9573585 | snp | A/G | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558776 | GGTGTCTGTGATTCA[A/G]CCATGTACAGTGCTA | 7347 |
rs9573586 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565039 | tgatagtgCGGTCCA[C/G]CCAGTAAATCATAGG | 7347 |
rs9573587 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594489 | CTTAAAATTTAACTC[C/G]AAAAGAGTTTCTTTA | 7347 |
rs9573588 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600687 | gtaatccaagaagtc[C/T]gatatagatatattt | 7347 |
rs9573589 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601634 | ctacagagtaatata[A/G]acataacttttatat | 7347 |
rs9593095 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552435 | GTTATTATAATCAAT[A/G]TGAGCAAATACTGCT | 7347 |
rs9593097 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565715 | gtcatttgctgaccc[C/T]GCTCTATTGGAAGCA | 7347 |
rs9593098 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575254 | TCCCACCGTGATTGT[C/T]TGGTAGATCAGCTAA | 7347 |
rs9593099 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576029 | agtgctggcattaca[C/G]gtgtgagccaccgcc | 7347 |
rs9593100 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581157 | AATTATTTTAACTAT[C/T]TACCCACTAATGATC | 7347 |
rs9593102 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581412 | ggcagtgcagtgggt[C/T]gatcttggctccctg | 7347 |
rs9593103 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599846 | tcaaaaactagaaat[A/G]attaagcttagtgag | 7347 |
rs9600493 | snp | C/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548950 | TCTGCAGCCACAGTG[C/G]GTTTTCCCTTCTTCA | 7347 |
rs9600494 | snp | A/G | 0.22263 | 0.248497 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553777 | CTGGATGTCTTATAG[A/G]TACCTTAAAGTTAAT | 7347 |
rs9600495 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556993 | aggccggggccagag[G/T]attgcttgagtgtag | 7347 |
rs9600496 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561511 | TTTAGAAATTTTAAG[C/T]ACTAGAATAAACTTA | 7347 |
rs9600497 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561861 | tatacatacgtatac[A/G]tatatacatacgtat | 7347 |
rs9600498 | snp | G/T | 0.249886 | 0.25 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573767 | ttcaaatatagtcac[G/T]ttgaaggttagggct | 7347 |
rs9600499 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574184 | gattgtgccactgta[C/T]tccagcctgggcaac | 7347 |
rs9600500 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580507 | AGATGTTCCCAATTA[C/T]TTTCTTTTCCATGTG | 7347 |
rs9600501 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603693 | ATTTTAAGAAGACAT[C/T]TTATGATATATTATT | 7347 |
rs9600502 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603822 | AAAGGTTCTTAGAAA[C/T]TTTAGGAATTATGTC | 7347 |
rs9600503 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605042 | TGTAAAAATTGAAAA[A/G]GCAAGAATAGTATTG | 7347 |
rs10162059 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603043 | cacccaggctggagt[A/G]cagtggcatgatcat | 7347 |
rs10162224 | snp | C/G | 0.258843 | 0.249844 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592386 | CCAAAATGGTGTTTG[C/G]ATGTAAAGTGGAATT | 7347 |
rs10581965 | in-del | -/T | 0.471292 | 0.116318 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550736 | CCTTATTTTACCCTG[-/T]TTTTTTTTTTTTTTT | 7347 |
rs11310964 | in-del | -/T | 0.483923 | 0.0882034 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581348 | TAAACACTTGATTTC[-/T]TTTTTTTTTTTTTTT | 7347 |
rs11330521 | in-del | -/T | 0.483852 | 0.0883933 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581517 | ATCACACCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 7347 |
rs11364688 | in-del | -/T | 0.415727 | 0.187175 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595788 | GGCTTATACCTGTAC[-/T]TTTTTTTTTTTTAAG | 7347 |
rs11555620 | snp | A/G | | | missense | UCHL3 | GRCh38.p7 | 13:75567287 | TGAGCCCTGAAGAAC[A/G]AGCCAGATACCTGGA | 7347 |
rs11616632 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557511 | TTTTTTGGTTATTTT[A/G]TTACTCAATATTTAA | 7347 |
rs11616942 | snp | C/G | 0.0854556 | 0.188216 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565673 | acttatgaaaagagg[C/G]agtgggccagatttg | 7347 |
rs11617067 | snp | C/T | 0.225893 | 0.248835 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576802 | GCCCTAAATGAAATA[C/T]GGTTGAATGTTCTAC | 7347 |
rs11840829 | snp | A/C | 0.140581 | 0.224783 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561961 | TTATAATAGATTTTG[A/C]GGCTATATCCTTCTG | 7347 |
rs11841712 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557101 | atgcctgtagtctca[A/G]ctatctgggaggctg | 7347 |
rs12857805 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547776 | ctggggtgtgctagg[A/C]caacctctgtaaggt | 7347 |
rs12859594 | snp | C/T | 0.100588 | 0.200439 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586666 | aaaatttaatttata[C/T]aaagaatgttttcta | 7347 |
rs12859711 | snp | A/G | 0.093777 | 0.195178 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586798 | caaagaggaatcaca[A/G]gagaaattagaaaac | 7347 |
rs12861744 | snp | C/T | 0.101658 | 0.201233 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586562 | tttggaatacaacag[C/T]tgaatatacagtctt | 7347 |
rs12861774 | snp | A/G | 0.100588 | 0.200439 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550982 | aggtttttggtaaat[A/G]ttttttaaatcaggc | 7347 |
rs12865634 | snp | A/G | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555228 | GTCATCTGTGGCTCA[A/G]GTTCAAGTCATCTCA | 7347 |
rs12865730 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555183 | CTTTGCTTGAGTCAT[C/T]CACTCCTGTTTGTTT | 7347 |
rs12865770 | snp | A/C | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555311 | atcctcacttgtttt[A/C]ttttcttcacagtac | 7347 |
rs12865911 | snp | G/T | 0.0397787 | 0.135303 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599152 | ttttttttttttttt[G/T]gtaaattggggtcta | 7347 |
rs12866456 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585853 | atcttgtaaatcctc[A/G]ggcaattactgaaaa | 7347 |
rs12870619 | snp | C/G | 0.093417 | 0.194889 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561769 | TCTAGAATGATATAT[C/G]TGTATGTTTCTGTGT | 7347 |
rs12870664 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561845 | CGTATATACGTATAC[A/G]TATACATACGTATAC | 7347 |
rs12871445 | snp | C/T | 0.100231 | 0.200173 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561764 | TTTTTTCTAGAATGA[C/T]ATATGTGTATGTTTC | 7347 |
rs12872149 | snp | A/T | 0.499995 | 0.00159744 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588297 | TCTAGATTCTTAGAA[A/T]TTTTTTTCTCCACTA | 7347 |
rs12872420 | snp | G/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579829 | AGAGGGTAATGTTAG[G/T]ATATAAGATTTTTTT | 7347 |
rs12872971 | snp | A/C/G | 3.30349e-05 | 0.00406403 | missense | UCHL3 | GRCh38.p7 | 13:75567238 | TCAGAATCTGGATCA[A/C/G]CCTTGAAAAAATTCC | 7347 |
rs12873322 | snp | G/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567193 | TCTCTGCTGTATCAA[G/T]CCTTTTTAATTTTAT | 7347 |
rs12874039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561872 | atacatatatacata[C/T]gtatatacgtataca | 7347 |
rs12876895 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604961 | CTAGAAAATCCAAAA[A/G]GAAAATTTATATTAG | 7347 |
rs12877244 | snp | C/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604962 | TAGAAAATCCAAAAA[C/G]AAAATTTATATTAGT | 7347 |
rs13378544 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605305 | ctgaggtcaggagtt[C/T]gagaccagcctgacc | 7347 |
rs13378810 | snp | C/G | 0.157972 | 0.232445 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559462 | TAAACATACCTAGAA[C/G]CTTATTTTTGACCAA | 7347 |
rs17064655 | snp | C/G | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548472 | AATTTCCTCTATTAG[C/G]TGCAGAATAGTAATA | 7347 |
rs17064713 | snp | A/C | 0.102726 | 0.202016 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579268 | CAGGCGGAAACAATA[A/C]ATGTATCATGCGGTT | 7347 |
rs17702733 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575526 | GCTACAGAAGTTTGA[A/T]ATGTGTCATTTAATT | 7347 |
rs17703316 | snp | G/T | 0.084364 | 0.187256 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596558 | AACTTCAAGAAAGTA[G/T]ATTTGGCCAGAGCAA | 7347 |
rs28420679 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565458 | TTTCTTCCATAGGCA[A/G]GAGATAAAAGAAGCA | 7347 |
rs28498482 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561773 | GAATGATATATGTGT[A/G]TGTTTCTGTGTGTGT | 7347 |
rs28659861 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563159 | TATGTATGTATGTAT[A/G]TATGTATATATATGT | 7347 |
rs33990256 | in-del | -/TGTCTTGTCT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572017 | GTCTTGTCTTGTCTT[-/TGTCTTGTCT]GTCTTGTCTTTACTT | 7347 |
rs34072684 | snp | A/G | 0.100588 | 0.200439 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591112 | GAAGTCTGATTACAC[A/G]TACATTTAATGCTTA | 7347 |
rs34099087 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590476 | CATTTAGTTGACTCA[-/G]GGTCAACAAATGCTG | 7347 |
rs34100020 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559046 | TCAGCCCCGGACTCT[-/T]TTTTTTTTTTTTTTT | 7347 |
rs34230855 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586043 | TCAGTATAAAGACTC[-/A]AAATGTCTATAAACC | 7347 |
rs34241221 | snp | C/T | 0.093777 | 0.195178 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573169 | TTTGGGAGGCTGAGG[C/T]GGGAGAATCGCTTGA | 7347 |
rs34359640 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578245 | GTGAGTAAACCACAA[-/T]TTATTTTTCATTTCC | 7347 |
rs34401287 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577311 | TGAATATATACAGAC[-/T]TTTTTTCTTGTCATT | 7347 |
rs34407556 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599272 | CACTGCACACAGGCC[A/G]TAGTTTTAATTTTTA | 7347 |
rs34509734 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585314 | TCAAGGCAGCCACAT[-/G]AAAAAGACAGAGTAG | 7347 |
rs34594704 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561439 | ATTTTCTTCTTTAAT[-/A]AAAATTTGGTTAGTT | 7347 |
rs34729024 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559856 | TGTAATGATGTACTT[-/A]AAAAGTTATCAGCTT | 7347 |
rs34792229 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556881 | TGGCAGGTGGCCTCG[-/A]AAAAGCACTTAACCT | 7347 |
rs34858184 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557366 | AAAATTTGTCATTGG[-/T]ACCATAGAATAAAAA | 7347 |
rs34879505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551795 | TGGACCTTGTTTCTA[A/G]GGTGTCTTGAAAAAC | 7347 |
rs34882632 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571339 | ATGATCTTCATGTCT[-/A]CTTTTTTCAGACCTA | 7347 |
rs34949196 | snp | C/T | 0.101658 | 0.201233 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603196 | GGTCTCACTGTATTG[C/T]CCAGGCTGGTGTTGA | 7347 |
rs35022480 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564155 | GGAAGTGCAGATATC[-/T]TTTTTTTTTTTTTGA | 7347 |
rs35046569 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552036 | TAATACATGGAATAG[-/T]GACAGGAGACCTTTC | 7347 |
rs35132045 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605675 | GAAATGTTTATCATT[G/T]GTAAGTAAAACACTT | 7347 |
rs35132275 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551513 | AATTCATATTAAGAA[A/G]ACTGCAAATCAGTAT | 7347 |
rs35178906 | in-del | -/T/TT/TTT | 0.539662 | 0.220494 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590177 | GTGACAAGGGCTGTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 7347 |
rs35349635 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603260 | GTGTGAGCCACCACA[-/C]CCCAGCCATAACTGA | 7347 |
rs35350351 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561533 | TAAACTTAAATACAG[-/T]TTTTTTCAATATATA | 7347 |
rs35365245 | in-del | -/T | 0.499154 | 0.0205497 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581695 | CTCTGCTTTGTTTGA[-/T]TTTTTTTTTTTTTTT | 7347 |
rs35392579 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552178 | TGCTTTTAGTGGGAG[-/A]AATGGGCAAGTATGT | 7347 |
rs35393925 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590929 | ACACTACAGAATTAA[-/G]GCAACTACAGCTCTT | 7347 |
rs35631959 | snp | C/T | 0.101301 | 0.200969 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552225 | TAAAAATTTTGTGGT[C/T]GTTTCTTTATTCTCT | 7347 |
rs35701234 | in-del | -/TCC | 0.351719 | 0.228371 | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75589938 | TTTTTAATTATGTAG[-/TCC]TCCTCGCCATCCTCA | 7347 |
rs35853105 | snp | C/T | 0.0879971 | 0.190408 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549252 | GGATATATAGAAACA[C/T]CCGCTGCCTCCCGCA | 7347 |
rs35853503 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599135 | CACCATGCCTGGCTA[-/T]TTTTTTTTTTTTTTT | 7347 |
rs36015067 | in-del | -/A | 0.541917 | 0.0926287 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602108 | CTGTCTCAAAAAAAA[-/A]CAAAAACAAAAACAA | 7347 |
rs36133915 | in-del | -/T/TATGTATATATG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592446 | ATATATATGTATATA[-/T/TATGTATATATG]GTATATATATATATA | 7347 |
rs36147336 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592549 | ATTTTTTGAAACAAG[-/C]ACTTGCTGAAATTTG | 7347 |
rs55777620 | snp | A/G | 0.316243 | 0.241064 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601970 | AAAAATTAGCTGGGT[A/G]TGGTGGTGGGTGCCT | 7347 |
rs55927305 | snp | A/G | 0.319856 | 0.240042 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561213 | GCTGGGCTTATAGGC[A/G]TGAGCCACTGTTCCC | 7347 |
rs55995428 | snp | A/C | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551352 | AGGAGAATCGCTTGA[A/C]CCCGGGAGGCGGAGG | 7347 |
rs56117705 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581538 | TTTTTTTTTTTTTTT[-/T]AGTAGGGTGGGGTCT | 7347 |
rs56262060 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575240 | CCTACTTTTCTCCAT[C/T]CCACCGTGATTGTCT | 7347 |
rs56383676 | snp | C/G | 0.105924 | 0.204309 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588363 | CATCATTTATTTCCC[C/G]TTTTTATTCATTGCC | 7347 |
rs56723936 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551446 | AAAAAAAAAAAAAAA[-/A]GACACTTCCTAACTC | 7347 |
rs56864940 | snp | A/G | 0.102726 | 0.202016 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565493 | CTTAACTACTTGTAG[A/G]TTTTCTATAGACATC | 7347 |
rs56868157 | in-del | -/TA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563605 | ATATCTATCATCACA[-/TA]GTTACTTTTTTTGTT | 7347 |
rs56945758 | in-del | -/T | 0.0268433 | 0.112699 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566679 | AAATACACTGTTGAC[-/T]TTTTTTTTTTAATAG | 7347 |
rs57223069 | in-del | -/AA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551446 | AAAAAAAAAAAAAAA[-/AA]GACACTTCCTAACTC | 7347 |
rs57667166 | snp | A/G | 0.000411736 | 0.0143422 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550038 | CTTTTCTGTCTGCTC[A/G]GTCCGCTTCCCTGCT | 7347 |
rs57960178 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594591 | TTCATTTCATTCAGT[-/C]AAGTATGCAATGTGC | 7347 |
rs57994648 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550721 | CCTTATTTTACCCTG[-/T]TTTTTTTTTTTTTTC | 7347 |
rs58156788 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587342 | TGAATAAATTTAATA[A/T]CTGTGCTTAGATTAG | 7347 |
rs58619365 | in-del | -/A/AA | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587035 | AAAAAAAAAAAAAAA[-/A/AA]GAGCAAATTAAATCC | 7347 |
rs58677064 | in-del | -/GTGTGT/GTGTGTGT | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563943 | TGTGTGTGTGTGTGT[-/GTGTGT/GTGTGTGT]CTATATCTATGCCAC | 7347 |
rs58733406 | in-del | -/AAA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595627 | AAAAAAAAAAAAAAA[-/AAA]GAGCGTAATAGTTGT | 7347 |
rs59431359 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590731 | TTTCTAAAGATCTTT[C/T]CCAAGTAGGAAATGA | 7347 |
rs59542200 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556418 | TCAAGTAATTGCTAG[A/G]TAAGTATAATTTTAC | 7347 |
rs59549415 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556070 | TCATAAAATATGCCT[C/T]CTATAGGCATATTTT | 7347 |
rs60083157 | snp | C/T | 0.145978 | 0.227331 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594573 | ATACATATCAGTTCA[C/T]GTATTCATTTCATTC | 7347 |
rs60286286 | in-del | -/T/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590178 | TGACAAGGGCTGTCT[-/T/TT]TTTTTTTTTTTTTTT | 7347 |
rs61398542 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582106 | CTTTGGGCAAGTCAA[G/T]TAGGTCCTTGTGCTT | 7347 |
rs61453475 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599152 | TTTTTTTTTTTTTTT[-/T]GTAAATTGGGGTCTA | 7347 |
rs61459966 | in-del | -/CAAAT | 0.499992 | 0.00199679 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586458 | TCAGAATCAATAAAA[-/CAAAT]AGATACAGAACATTA | 7347 |
rs61472085 | snp | G/T | 0.139225 | 0.224118 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549599 | GAAATTGGCTTATTT[G/T]TTTCTCCTCGGCAGC | 7347 |
rs61959727 | snp | A/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555617 | GGTTTAATTTTTTAT[A/T]ATAATAATATATAAG | 7347 |
rs61959728 | snp | A/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561287 | GATAAATACAATCTT[A/T]AAGAACAAATGATCC | 7347 |
rs61959729 | snp | C/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563944 | TGTGTGTGTGTGTGT[C/G]TATATCTATGCCACC | 7347 |
rs61959730 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563946 | TGTGTGTGTGTGTCT[A/G]TATCTATGCCACCTT | 7347 |
rs61959731 | snp | G/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572033 | GTCTTGTCTTTACTT[G/T]TCCTTCCTTCCTTCC | 7347 |
rs61959732 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572036 | TTGTCTTTACTTTTC[C/T]TTCCTTCCTTCCTTC | 7347 |
rs61959733 | snp | A/C | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572039 | TCTTTACTTTTCCTT[A/C]CTTCCTTCCTTCCTT | 7347 |
rs61960592 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592301 | GTAGGATCCTTATCA[A/G]TAGATAGAGACATAC | 7347 |
rs66497962 | in-del | AC/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594591 | ATTCATTTCATTCAG[AC/T]AAGTATGCAATGTGC | 7347 |
rs66808557 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547420 | GGCAGGTTCAAAATG[A/C]AAAACCCATAAATAA | 7347 |
rs67270540 | snp | C/T | 0.101658 | 0.201233 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586030 | AAGTTAATGAAATGT[C/T]AGTATAAAGACTCAA | 7347 |
rs67532728 | in-del | -/TTATGTAT | 0.940825 | 0.104371 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563127 | GTACCTCATTATCCT[-/TTATGTAT]GTATGTATGTATGTA | 7347 |
rs67656352 | snp | C/T | 0.101658 | 0.201233 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587858 | GGAACAAAGAGCCTG[C/T]TTGCTTACTGCTTGC | 7347 |
rs67777133 | in-del | -/T | 0.499382 | 0.017561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592495 | ATCCCATCTATAGCC[-/T]TTTTTTTTTTTTTGC | 7347 |
rs68044755 | snp | A/G | 0.102014 | 0.201495 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561558 | TATATATATATATAA[A/G]GAATCTTCTTTGCTT | 7347 |
rs68176896 | in-del | -/CTC | | | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75589943 | AATTATGTAGTCCTC[-/CTC]GCCATCCTCATCACA | 7347 |
rs71127556 | in-del | -/GTATATACGTACGTATATACGTATACGTATACATACGTATAC | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561860 | TATACATACGTATAC[lengthTooLong]ATATATACATACGTA | 7347 |
rs71127557 | in-del | -/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564162 | TCTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 7347 |
rs71127558 | in-del | -/GTCTTGTCTT | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572027 | GTCTTGTCTTGTCTT[-/GTCTTGTCTT]TACTTTTCCTTCCTT | 7347 |
rs71127560 | in-del | -/CATATATATATATATGTATATATGTATATA | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592452 | ATATATACATATATA[lengthTooLong]TATATATATATATAT | 7347 |
rs71201184 | in-del | -/A | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573382 | TTTGTCAGTTCCTAC[-/A]AAATACATAGGTCTT | 7347 |
rs71201185 | in-del | -/ATTT | 0.486398 | 0.0813386 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578244 | TGTGAGTAAACCACA[-/ATTT]ATTTTTCATTTCCTT | 7347 |
rs71433191 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554328 | TTCATTTCTTATAAT[A/C]TCTTCTAATCTTGTA | 7347 |
rs71433192 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581914 | TAAGTTTGACAACCA[A/G]AAGATAGATTTGGAT | 7347 |
rs71433193 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584615 | TGTCTGGCTTTTAAC[C/G]AAAAGCATTCAGCAG | 7347 |
rs71433194 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590318 | TTTGCCAGTGCCTCA[A/G]AACATCCATCTTTCC | 7347 |
rs71670998 | in-del | -/AGA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603687 | AAGGATATTTTAAGA[-/AGA]CATTTTATGATATAT | 7347 |
rs71756853 | in-del | -/AT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561541 | AATACAGTTTTTTCA[-/AT]ATATATATATATATA | 7347 |
rs71826804 | in-del | -/AAAA | 0.258843 | 0.249844 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597372 | AAGACGTCATCTCTT[-/AAAA]AAAAAAGAAAAGAAG | 7347 |
rs71993215 | in-del | -/TTGT | 0.225597 | 0.248806 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594231 | AGTCTTAATTTCAAA[-/TTGT]TTGTTAAGCATCAAA | 7347 |
rs73223960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547298 | GTATCACCTTGCTCA[A/G]CCTTGGCTGGGAACT | 7347 |
rs73223968 | snp | A/C | 0.31721 | 0.240796 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567585 | TGCAGTCTCGCTCTG[A/C]CGCCCAGGCTGGAGT | 7347 |
rs73223971 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586270 | TTCCCAGTGTTGAAG[A/G]AGGACATTACATAAG | 7347 |
rs73223973 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589740 | TAGAACTATGGCATA[C/T]AACCTGATACTTGGT | 7347 |
rs73223981 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604545 | TGTAATAAATTCCGT[C/T]CATGAAGATAATTTA | 7347 |
rs73223982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605234 | CACTTACGGCCAGGC[A/G]TAGTGGCTCACGGCT | 7347 |
rs73541475 | snp | G/T | 0.0955749 | 0.196603 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550492 | CCCGCCACGCCCCCT[G/T]TATCTTCCAGTCTTT | 7347 |
rs73541490 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575220 | TGCTCTAGAGTAATT[A/G]TTTACCTACTTTTCT | 7347 |
rs74094447 | snp | A/G | 0.140242 | 0.224618 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571281 | CTTGCCCCATTTTTG[A/G]AGTTTCATCCAAATT | 7347 |
rs74094448 | snp | A/G | 0.140242 | 0.224618 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571535 | CCACTGTAACTATCT[A/G]GGACAAATTCATTAA | 7347 |
rs74094449 | snp | G/T | 0.11963 | 0.213316 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586758 | TTTAGATATTCAATA[G/T]TACACTTCTAAATAA | 7347 |
rs74094452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589866 | ACAAGCATGACCATA[C/T]GTTGCTTTTAAGAAT | 7347 |
rs74094453 | snp | C/G | 0.0119575 | 0.0763923 | intron-variant, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75589943 | AATTATGTAGTCCTC[C/G]TCGCCATCCTCATCA | 7347 |
rs74094454 | snp | A/C | 0.104149 | 0.203046 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591431 | AGGTGAACTAAATGA[A/C]CAGGGTAGAATCCTA | 7347 |
rs74201049 | in-del | -/CATA | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592448 | ATATATATATATATA[-/CATA]TATACATATATATAT | 7347 |
rs74347401 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600340 | TGACTAGCCTTCTCT[G/T]GGGAAGAAGATGCCA | 7347 |
rs74493971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553578 | CCAACTTCTAAGGAG[C/T]GCCTCAGCCACTTCA | 7347 |
rs74617651 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566955 | AAACTATAAAATAAA[A/G]CATTCCCTGCTTCCT | 7347 |
rs74690679 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594417 | ACTGTTTACACTGCA[C/G]TGTTGAAACATCAGA | 7347 |
rs74742033 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576828 | TCTACTAGAAAAATA[A/G]TTACTGATTTTAAAA | 7347 |
rs74795858 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590192 | CTTTTTTTTTTTTTT[-/TT]CTTAACTTCGGTCTT | 7347 |
rs74965873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589766 | TTGGTTATATATTTC[C/T]ACTTTACCTGCTTTT | 7347 |
rs75021921 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565159 | TTCCTTTAGTTGCTT[C/T]GTATCATTTTAGGAA | 7347 |
rs75195681 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586944 | GGTTAGAGGGAAACT[A/G]TAGTATTACATGCTT | 7347 |
rs75250872 | snp | C/T | 0.0387781 | 0.133862 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590873 | AATTATCTTAAATGT[C/T]GAGACTGATGATGCA | 7347 |
rs75348506 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593732 | TTTGAGGGAAATAAC[C/T]TCTGAAGAATAATGT | 7347 |
rs75375758 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585297 | AGATAAATGGAAAAT[G/T]TTCAAGGCAGCCACA | 7347 |
rs75531503 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565131 | ATTTTTTGATCTACC[A/G]TAATTTCTTTTTTTC | 7347 |
rs75608588 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558030 | TTTCTCCATTTCCCA[C/G]AGGTAGTCTTTATAG | 7347 |
rs75612284 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591079 | TATAAATTATGATGG[C/G]TTTTGAAGCCAGAGG | 7347 |
rs75651516 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576417 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACAGT | 7347 |
rs75944896 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566688 | GTTGACTTTTTTTTT[-/TT]AATAGTATGAAGTAT | 7347 |
rs75968555 | snp | G/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572028 | GTCTTGTCTTGTCTT[G/T]ACTTTTCCTTCCTTC | 7347 |
rs76036910 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591636 | TAAATGTTTTTGTAG[A/C]TTAGTAGTAAAGAAC | 7347 |
rs76329592 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573269 | GACTCTGTCTCAGAA[A/G]AAAAAAAAAAAAAAA | 7347 |
rs76359710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586556 | CAGAAATTTGGAATA[C/T]AACAGTTGAATATAC | 7347 |
rs76659378 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573268 | AGACTCTGTCTCAGA[A/G]AAAAAAAAAAAAAAA | 7347 |
rs76752172 | snp | A/G | 0.030278 | 0.119257 | intron-variant | COMMD6 | GRCh38.p7 | 13:75546939 | TGAGCCTGTGGTCAC[A/G]ATATTTTCATTAGCT | 7347 |
rs76781174 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586638 | TTAAAAAATCAACCT[G/T]AAATTTTTTTAAAAA | 7347 |
rs76873344 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582990 | CACTGTTATGTCTAT[A/C]TTATGCATTATCTCT | 7347 |
rs76947068 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551433 | AAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAGA | 7347 |
rs77099327 | snp | G/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564168 | ATCTTTTTTTTTTTT[G/T]GAGATGGAGTCTCGC | 7347 |
rs77280463 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602393 | TACCAAAAAGTCAGG[A/C]CACTATTTTCTTCCC | 7347 |
rs77297479 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604366 | TAAGCCATGACAGTG[C/T]AGCTCCCTTTCATTG | 7347 |
rs77313445 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587360 | GTGCTTAGATTAGAT[C/T]CTGGGGGAAATGCTA | 7347 |
rs77574505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592368 | CAGGCAGCAGCTTCA[A/G]AGCCAAAATGGTGTT | 7347 |
rs77945818 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574348 | AGTCAATAATAAGTT[G/T]TTTCTTCCTTGTGTA | 7347 |
rs77946332 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598593 | TACTTTGAGATTATC[C/T]TCCAATTTAGGCCAT | 7347 |
rs78417507 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565312 | CCTTTCCAGTTTTTT[A/G]TCAATCGAACTTACA | 7347 |
rs78554179 | snp | C/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572454 | CATCTTAGTGGTTCA[C/G]AAAATGGTGTGTCAT | 7347 |
rs78774974 | snp | C/T | 0.0364509 | 0.129988 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548665 | CAAGTGATGTTTCTG[C/T]ATATCTGATCATCCC | 7347 |
rs78963960 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573266 | CGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAAAA | 7347 |
rs78994124 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596048 | CTCATTTGCTGTCTA[C/T]ATATTACCTTGTCAC | 7347 |
rs79021024 | snp | A/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572029 | TCTTGTCTTGTCTTT[A/T]CTTTTCCTTCCTTCC | 7347 |
rs79193778 | snp | C/T | 0.00101381 | 0.0224917 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590149 | GTTTAGTCAATCTTC[C/T]GTCTCTTCTTCCAGT | 7347 |
rs79198640 | snp | A/T | 1.89006e-05 | 0.00307407 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566689 | TTGACTTTTTTTTTT[A/T]AATAGTATGAAGTAT | 7347 |
rs79224772 | snp | A/G | 0.02016 | 0.0983543 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606486 | AATGTGGAGTCCCTA[A/G]AGTAGGAACATCTTG | 7347 |
rs79358332 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565905 | CAGCTGAGCCAGGAC[A/G]TGGGCCCAGGCAGTC | 7347 |
rs79442292 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579107 | CCAAAAATGATTTAC[A/G]CACAAATTGAGGTGC | 7347 |
rs79445103 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570945 | ATTGGTTGCTCTAGG[C/T]GCTGCTTTCAAAGGT | 7347 |
rs79473030 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586755 | ATATTTAGATATTCA[A/G]TAGTACACTTCTAAA | 7347 |
rs79619454 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589538 | TCTTTTTTACCAATG[C/T]CTATCACCACACAGT | 7347 |
rs79621056 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582191 | TCTGTGTGTGTAAGT[G/T]AATGTGTGTGTGTGT | 7347 |
rs79624821 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585153 | TACAGACATCAAACC[A/G]CAGCTTCAGGAATCT | 7347 |
rs79629463 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552764 | GTTACAGATAATTAA[A/G]CATCAAGAATTACAA | 7347 |
rs79696017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601398 | TGGCAAACTTCATTA[G/T]TGTCTTATTTTAGGA | 7347 |
rs79788358 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581363 | TTTTTTTTTTTTTTT[C/T]CCTTGAGACAGGGTC | 7347 |
rs79798506 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583233 | AAAAATAAACAATTA[C/T]AATATATTGATATGC | 7347 |
rs79988056 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562290 | ATAAAAGAAATGATA[C/T]TTCTTTGCATTTACT | 7347 |
rs80015606 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551430 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 7347 |
rs80019912 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593792 | TTTTAGAAACATTCT[C/G]TATATCCAAGATAGT | 7347 |
rs80081116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581913 | TTAAGTTTGACAACC[A/G]GAAGATAGATTTGGA | 7347 |
rs80122107 | snp | G/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564167 | TATCTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 7347 |
rs80141954 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580742 | TGATCCTCTCAACTC[C/T]GTAAGATAGCTGTTA | 7347 |
rs80150348 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573337 | GTATTATTATCTCCA[C/T]TGCTGTTTGTATTCC | 7347 |
rs80193046 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578476 | AGCACCTACTGTACT[A/T]GGCACTGTGCTTATA | 7347 |
rs111332834 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592433 | ATATATATATATATA[C/T]ATATATATATATATA | 7347 |
rs111478700 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576414 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 7347 |
rs111551475 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603518 | ATATATATTAATTTA[A/T]AATTTGGTTAGGGAG | 7347 |
rs111554688 | snp | C/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586401 | TGTTAGAACTGAAAA[C/G]AGAAATAGACAAATT | 7347 |
rs111626920 | snp | C/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569140 | ATGCTTACTTTATTC[C/T]AGTCTCAATTGAATA | 7347 |
rs111653662 | snp | A/G | 0.5 | 0 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560818 | TGGAATGGATCCTGA[A/G]CTCCTTAGCATGGTA | 7347 |
rs111703516 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594242 | CAAATTGTTTGTTAA[A/G]CATCAAAGCAAGAGA | 7347 |
rs111728295 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597017 | ATGAGTTTAAATAAT[C/T]TCAGAGTGGTAAAGA | 7347 |
rs111831497 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570589 | TATACTTAAAAAAAC[C/T]TGAAAAGAATACTTG | 7347 |
rs111850371 | snp | C/T | 0.5 | 0 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605072 | GAAAGACTTGCTCAT[C/T]ATATCCGAGATTTCA | 7347 |
rs112109558 | snp | C/G | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570474 | ATCTCCTGACCTTGT[C/G]ATCCACCTGTCTCAG | 7347 |
rs112263030 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589151 | TCTAGAACTTGATTT[A/C]CTGGGTCTGAATCCC | 7347 |
rs112313138 | in-del | -/T | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549595 | TAGGAAATTGGCTTA[-/T]TTTTTTTCTCCTCGG | 7347 |
rs112498729 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603142 | CTACAGACTTGTGCC[A/G]CTATACCTGGCTAAT | 7347 |
rs112595696 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573676 | TCCTGTTCTTATAAG[A/G]ATACCAGTCCTGTTG | 7347 |
rs112597363 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605981 | GCTCCAGGTTAAAGG[C/T]GCAATGCTTTCCTCC | 7347 |
rs112759858 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593629 | GATAACTCTGATTGC[G/T]AACACCTGTGGAATT | 7347 |
rs112780059 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585646 | TTGTTTTACATTTCA[A/G]TAAAAGATGATTAGG | 7347 |
rs113435747 | snp | C/T | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594695 | TTGAGATTAAGAAAG[C/T]TGTGCTTTTAGTCAC | 7347 |
rs113489349 | snp | C/G | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592284 | CTATTTATACTAAAA[C/G]AGTAGGATCCTTATC | 7347 |
rs113684362 | snp | A/G | 0.5 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583061 | TTAGCATGAGGAGGT[A/G]AAAATAAGTCTGACT | 7347 |
rs113767077 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570441 | CGGGGTTTCCCCGTG[G/T]TAGCCAGGATGGTCT | 7347 |
rs113797877 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569916 | ACATCATTTTCTTTG[C/T]TCAATAAATTTGTTT | 7347 |
rs113906326 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581832 | GCATGCACACTAACT[C/G]TGAAGGAAAAGTAAT | 7347 |
rs114009079 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581425 | GTCGATCTTGGCTCC[C/T]TGTAGCCTTGATCTC | 7347 |
rs114010115 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559774 | TCTTGAGGTAAGATA[C/T]AGTGATGCATTTTTA | 7347 |
rs114013146 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604572 | TTTAGGCTTTCAAAT[A/G]TGGAAGCAAAGTTCT | 7347 |
rs114063286 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564684 | GATAATTACCATCAA[C/T]GATAGTGTTGTGTTG | 7347 |
rs114265517 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591989 | GAGGTTTTGGAGCAT[C/T]TGAGATTTCAGATTT | 7347 |
rs114416274 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596814 | TATCAAGGGTAAGCT[A/G]CATATGAAGAATGAT | 7347 |
rs114633971 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547112 | TCTCTGTAAGGCACA[C/T]GAAAGCCTCCTTGGG | 7347 |
rs114644446 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594142 | GTATCGACTTTGCAT[A/G]TGTTATTTGAATGCC | 7347 |
rs114671978 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591523 | ACTTAAAAATGTTCC[A/C]AATATAAATGAACAT | 7347 |
rs114809660 | snp | A/T | 0.021333 | 0.101051 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586648 | AACCTTAAATTTTTT[A/T]AAAAAATTTAATTTA | 7347 |
rs114812350 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75604119 | CTTAATGAAGAGCCA[C/G]TTACAAGACATCTGA | 7347 |
rs114813923 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562411 | TGACATTTGTAGAAG[A/G]GTTGAGACAAAAACT | 7347 |
rs115117640 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557193 | TGCACTCCAGCCTGG[G/T]CAATGGAGCAAGACC | 7347 |
rs115230465 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596576 | TTGGCCAGAGCAAAC[A/G]TATGTAGGATTCATA | 7347 |
rs115239155 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600123 | TTCAGTTCTGTTAAG[G/T]CTGAGAGAGGTGAGG | 7347 |
rs115459038 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603305 | TAGTCTCATGAATGA[C/T]ACACACACAGAAATG | 7347 |
rs115472491 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580065 | GAAAAAAGTCTTTTT[A/C]GAATATCTTGATGTC | 7347 |
rs115531186 | snp | A/G/T | 0.0334801 | 0.125627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555793 | GATGGAGGTCACACT[A/G/T]TGTTGCCCAGGCTGG | 7347 |
rs115581427 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556903 | ACTTAACCTCCCAGA[C/T]GTAGTTTTCTTATTG | 7347 |
rs115590907 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75601446 | CAATCTTCAGCAACC[A/G]CCGTCCTGATCAGTC | 7347 |
rs115651477 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559677 | TGTGATCATTCTTCA[A/G]GGAGAAATGCCTATG | 7347 |
rs115655761 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604304 | GTTATTTGGATTATT[C/T]CTCTATATTACTGCA | 7347 |
rs115699929 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574738 | TGGCAGAAGATGAGG[C/T]TGAAGTAATAGGGTG | 7347 |
rs115765745 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603420 | GGATTGCTTGAACGC[A/G]GGAGGTTAAGTTCAG | 7347 |
rs115767441 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591943 | GCAGTTAGCATTTCC[G/T]TTGAACATCCTGTTG | 7347 |
rs115823176 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601252 | AAGATTACATAAATG[A/T]AGTTGATAAAGCAGC | 7347 |
rs115829609 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553774 | CATCTGGATGTCTTA[C/T]AGATACCTTAAAGTT | 7347 |
rs115925306 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570056 | TCCTTCCATCTTTTC[C/T]TTCTTTCTTTCCTTC | 7347 |
rs115937785 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583203 | TGCCTGCCCCCAGGC[A/C]TTACAAAGTAGTTTA | 7347 |
rs115964374 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562838 | TAAGTAGAAAATGAT[G/T]TAAGTAAATATATAA | 7347 |
rs116003974 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594555 | TTCAAATTTTAAAAA[C/T]TCATACATATCAGTT | 7347 |
rs116004356 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557643 | AATGCATGTATAGAT[A/G]ATTATCTTTGTGAGC | 7347 |
rs116172082 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589170 | GGTCTGAATCCCGGT[C/T]CTGTTACCTACTGGC | 7347 |
rs116225180 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548007 | ACTGTCTTGCTGTCC[A/G]GCCTTGTGTCTCAGC | 7347 |
rs116328058 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603350 | AATACATATATTAAG[C/T]CAGGTGCTGTTGCAT | 7347 |
rs116414219 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561559 | ATATATATATATAAG[C/G]AATCTTCTTTGCTTA | 7347 |
rs116535756 | snp | A/G | 0.0248432 | 0.108648 | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549394 | CTGTCTCAGAATAGG[A/G]CTCCGCGGCACGCCT | 7347 |
rs116553491 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586345 | AGAAAGTATGTGTAT[A/G]CAGCTAACAATTAGA | 7347 |
rs116626047 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548815 | TTGGTGAAAAAGATA[C/T]ATGACAAATCCTGCT | 7347 |
rs116741494 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593768 | TAGGTGAAACACTAT[A/G]TATAAATGTTTTAGA | 7347 |
rs116859074 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587000 | AGTCAGAGATCTAAG[A/T]TTTTACCTTAAGGTA | 7347 |
rs116903958 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571760 | TTCTGGAGGGCTTTT[C/T]TACACTGCTGTGTAC | 7347 |
rs116934398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572734 | TAAACAAAACATATC[C/T]ATTAGCCATTGTTTC | 7347 |
rs117202683 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572735 | AAACAAAACATATCC[A/T]TTAGCCATTGTTTCC | 7347 |
rs117226556 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605419 | AGGCTGAGATAGGAG[A/G]TTTGCTTGAACCCGG | 7347 |
rs117326779 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555122 | TGTGCTGCAGTCTTC[A/G]AATGTGGAGTCTGTT | 7347 |
rs117431302 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579962 | TTAATGTAACATTTA[C/G]ATGTACAGGTATTAT | 7347 |
rs117526769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556105 | TGAGTAATCTATGTC[A/G]AGTACAGTGGGCTAT | 7347 |
rs117603542 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564153 | CATGGAAGTGCAGAT[A/G]TCTTTTTTTTTTTTT | 7347 |
rs117707698 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584248 | CAAGCCCACCATTAG[A/T]CTAGCAAGCACCAAG | 7347 |
rs117730948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558945 | GAGCAGGAAGTAGTT[C/T]GAAGTGCTTTAGTGA | 7347 |
rs117816072 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578014 | ACAGCAGTATTGTTT[C/T]CTGTTTTTAAATAAA | 7347 |
rs117855413 | snp | A/C/T | 0.0079613 | 0.0626594 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573872 | CACTTCCGGGTATAC[A/C/T]GCTGCTCTTTGCAGA | 7347 |
rs118108474 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576644 | CAGTCATGAGCCACC[A/G]CTCCTGGCCCTGAAT | 7347 |
rs118165555 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579236 | AAAATTTAAGTTGCC[A/G]ATTATCTTGTAAGAA | 7347 |
rs137968950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582488 | TGTCCTGGCAAACAT[A/T]GGTGTCGTTAATAGT | 7347 |
rs138030627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553237 | TGTTTTCCTTCTTTG[C/T]AAACTTTCCACAAAG | 7347 |
rs138178422 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588335 | GTCACCTCTCCTTCT[A/G]TCTCTTCCTTTACAT | 7347 |
rs138290692 | snp | C/G/T | 0.00358891 | 0.0422285 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604499 | CTGACAATAATTTTG[C/G/T]GTATTATTTTCAGGA | 7347 |
rs138321284 | snp | C/T | 1.76946e-05 | 0.00297439 | splice-donor-variant | UCHL3 | GRCh38.p7 | 13:75560883 | CTATTACAGAAAAGG[C/T]AATTGTTATGTAAAA | 7347 |
rs138344990 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563628 | TTTTTTGTTACAAGA[A/G]CAGCTAAAATCTTAT | 7347 |
rs138355808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557597 | ATGTAAATGGGATGC[C/T]TCTAATTAACTGTGT | 7347 |
rs138372594 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599132 | GCCACCATGCCTGGC[-/T]TATTTTTTTTTTTTT | 7347 |
rs138377793 | snp | A/C | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588092 | AAAAAGTAAGAGGCT[A/C]ACTGATTAAATTGAA | 7347 |
rs138596123 | in-del | -/ATA | 0.455144 | 0.142885 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555617 | GTTTAATTTTTTATT[-/ATA]ATAATAATATATAAG | 7347 |
rs138613709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577850 | ACTTAACTAAAAAGT[A/G]ATTCCTAAAATTTGT | 7347 |
rs138664847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561892 | ATACGTATACATATA[C/T]ACACACACATGCACA | 7347 |
rs138672487 | in-del | -/TA | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559922 | TTCTCATTTTTTCTC[-/TA]TGTGATAGATTAAGG | 7347 |
rs138711361 | in-del | -/TA | 0.0256215 | 0.110247 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568475 | ATTTTTTAGGGAGTG[-/TA]TATATATATATACAC | 7347 |
rs138712100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558550 | AAATTCTCTTATCAG[C/G]GTTCATGATACTTTT | 7347 |
rs138830150 | snp | C/T | 0.00957169 | 0.0685144 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549819 | GGCCGGGCACCGCGG[C/T]CATGGAGGGTCAACG | 7347 |
rs138849403 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594410 | CTCAAAGACTGTTTA[C/T]ACTGCACTGTTGAAA | 7347 |
rs138894386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75598952 | ATGGACTCATGGATT[C/T]CTACTTTACTTGAAT | 7347 |
rs138944407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551055 | CTTATGAATCTATGT[C/T]GACTTTTCGCAAATG | 7347 |
rs138959840 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605384 | GTGGTGGTATGTGAC[A/T]GTAGTCCCAGCTACT | 7347 |
rs139046616 | in-del | -/TAG | 0.486529 | 0.0809556 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552033 | ATGTAATACATGGAA[-/TAG]TGACAGGAGACCTTT | 7347 |
rs139171307 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590211 | TAACTTCGGTCTTCA[A/G]AGTGCTTTTCTCTTG | 7347 |
rs139288508 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584689 | GAATTTAAAATAATT[A/T]AATGCTCAAGTGGAA | 7347 |
rs139322595 | snp | C/T | 0.00032071 | 0.0126591 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569525 | ATTTCACATTTTTTC[C/T]AAATTTTTCTTGCTA | 7347 |
rs139363450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555436 | TCTGAAGTATGAGAA[C/T]GGTGCCAGGCTCACG | 7347 |
rs139371894 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571714 | GTAGAGCAGTGATTC[C/T]CAAGATGGAGTGCAG | 7347 |
rs139385260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573454 | TTACCAGGTGCCTTT[A/G]ACAACAGAAATTTAT | 7347 |
rs139438599 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575321 | CTTCATTAACTTACA[C/T]TGAAAGGTATTGCTT | 7347 |
rs139527340 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548037 | CAGATCCAATGCTGC[C/T]AGTGTCCCTGGAAGA | 7347 |
rs139593169 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554156 | AACCTTGGAATTCCT[A/G]GGCTCAAGCACTCCT | 7347 |
rs139606180 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579106 | GCCAAAAATGATTTA[C/T]GCACAAATTGAGGTG | 7347 |
rs139607812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601375 | TTCATAAAAGAAAGA[C/G]TCAAATGTGGCAAAC | 7347 |
rs139675725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583671 | ACATTTTCACTAAAG[C/T]GTAATTGTAGAAAAC | 7347 |
rs139751366 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590400 | CACATTCATGATAAT[A/G]TTTAAGTCTGGTTAA | 7347 |
rs139784344 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595121 | TAAAATTGATTTGAC[A/G]TAGCGACAGTTTTCC | 7347 |
rs139817216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571397 | TGCCTGTTAGACATC[A/G]TCTGAATGACCTCAC | 7347 |
rs139878255 | snp | C/T | 8.25389e-05 | 0.0064236 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605790 | AACTAAGATTTAATG[C/T]GATTGCTCTTTCTGC | 7347 |
rs139886545 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595649 | AATAGTTGTAATGAT[C/T]GGGCTGAGTGTCACT | 7347 |
rs139952677 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548330 | AGAGGAGTTAAGGTA[A/G]TGAAATACCTCTGAA | 7347 |
rs140028437 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589841 | TTAAAAATAGTAGAC[C/T]ATATGAATTACAAGC | 7347 |
rs140089476 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606113 | TTCCATCTGCATAAC[A/G]TGAATATATATTATC | 7347 |
rs140317040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597222 | TTAGCACTGGGCACA[A/G]TGGTGTGTTCCTGTA | 7347 |
rs140342391 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565663 | ATGAAATTTTACTTA[C/T]GAAAAGAGGCAGTGG | 7347 |
rs140451739 | snp | A/C/G | 0.00478364 | 0.0487146 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560452 | TATAAATAAATTGCT[A/C/G]TCTCTTCTCACCCTA | 7347 |
rs140521127 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572596 | TACTGTTCCTTACAC[A/G]TAAGTACAACATATG | 7347 |
rs140676593 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564773 | CCATCTCAGCTCACT[G/T]CAACCTTTGCCTCCT | 7347 |
rs140676608 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585974 | AAAAAATAAAGAACT[A/G]ACAATGTAGATTTAA | 7347 |
rs140766132 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586910 | AAATGCTTATAGTAG[A/G]AAAAAACAAACAAAC | 7347 |
rs140867435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580018 | AATTATAAACTGAAG[G/T]GAGAGAAAACATAAT | 7347 |
rs141088547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581608 | AGTGATCTTTCTGCC[C/T]TGGCCTCCCAAAGTA | 7347 |
rs141213268 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596187 | AGATCGCATACTTTA[G/T]TAAAAAGAAATGGCC | 7347 |
rs141254050 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559540 | GGATAAGGATAGTTG[-/C]CCTTTAAACAGGAAG | 7347 |
rs141261662 | in-del | -/AGCCATAACTGAGTTTATT | 0.0383715 | 0.133092 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603264 | TGAGCCACCACACCC[-/AGCCATAACTGAGTTTATT]AGCTCTTTAGTCTCA | 7347 |
rs141319054 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562005 | AAATTAGAAACAGTA[A/G]GATGATTGCAGTAGT | 7347 |
rs141328876 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551250 | AGACCAGTCTGGCTG[G/T]TGAAACCCCGTCTCT | 7347 |
rs141425477 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562903 | AACATGTAAGTAGAG[A/T]ATATAAATAGCATGT | 7347 |
rs141467867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | COMMD6 | GRCh38.p7 | 13:75546870 | GTTGCCGTGAACACT[A/G]AATTAGCAAATACTA | 7347 |
rs141544733 | snp | A/C/T | 0.00795939 | 0.0626292 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575079 | TACTCTCTATCAGAA[A/C/T]GTTTTCATGGGAATG | 7347 |
rs141605427 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578349 | TAAGTATTCTTTTGG[A/G]TAGCTTCTTGTAGGT | 7347 |
rs141609949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577901 | GGAGCCAGCCCAGAT[A/G]TGGGTAGAGATCACC | 7347 |
rs141847540 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605178 | TAGAATCAATGAAAC[A/G]TGATTTTTAGTTGAA | 7347 |
rs141870275 | snp | G/T | 1.65704e-05 | 0.00287836 | missense | UCHL3 | GRCh38.p7 | 13:75566741 | AAATAAAATCTCAGG[G/T]ACAAGATGTTACATC | 7347 |
rs141889521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589275 | TGTGGGTTACTGGAA[A/G]GTTAAATGAACCTAT | 7347 |
rs141923066 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574044 | AACACAGTGAAACCC[C/T]GTATCTACTAAAAAT | 7347 |
rs141961386 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550926 | GCTCTCTATCTTAGG[A/G]AGGAAACATTTGATC | 7347 |
rs141970788 | snp | A/G | 0.000203752 | 0.0100913 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549855 | TGCCGCTGGAGGCCA[A/G]TCCCGAGGTGGGCGC | 7347 |
rs141987088 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570822 | GAGGCTGAGGTGGGA[A/G]GATTACTTGAGCTCA | 7347 |
rs141987941 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594623 | TATACTGTATACCAG[C/G]CATTGTGCTAAGTGC | 7347 |
rs142025720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556709 | TTGTATGCAAAAACC[C/T]GGAGGGAAGAGATGG | 7347 |
rs142041198 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599733 | TTTCCTCTCTTTGAA[C/G]TTCTCTATTCCCTGA | 7347 |
rs142309264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596553 | CTGTTAACTTCAAGA[A/G]AGTAGATTTGGCCAG | 7347 |
rs142355340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573158 | AATCCCAGCTATTTG[A/G]GAGGCTGAGGCGGGA | 7347 |
rs142418200 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575941 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 7347 |
rs142421905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601076 | TTAGAAGGGGAGCCT[A/G]AAGATGTGACTGAAC | 7347 |
rs142455646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554553 | TTTCAGCTGCCACAG[C/T]GCAAGCCACCATCCT | 7347 |
rs142465387 | in-del | -/AAG | 0.488545 | 0.074807 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603683 | ACAAAAGGATATTTT[-/AAG]AAGACATTTTATGAT | 7347 |
rs142528999 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564487 | GGTAGAGATTCATCT[C/T]CTTTACAAGGTGATT | 7347 |
rs142633100 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572414 | TATCTTACAGTTGAT[A/G]TCATAGTTTACTTGG | 7347 |
rs142766088 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580981 | TAAGTTACAAATAGT[A/C]ATTCAGAGTTGTGCC | 7347 |
rs142776013 | in-del | -/AAAAC/CAAAT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586454 | ACACTCAGAATCAAT[-/AAAAC/CAAAT]AAAAAGATACAGAAC | 7347 |
rs142890955 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583381 | TCCTTCCTCTGTTAT[A/G]TAAGTTTTTATTAGA | 7347 |
rs142970713 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595242 | AGCAAGAAAGTAAAA[A/G]CCATTACAGGGAACT | 7347 |
rs143020690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582772 | TTGCTTTAACAATTG[C/T]ATTAACAGTTAATAT | 7347 |
rs143085079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591888 | ATTAGACTTACCTGG[C/T]TGAGTATCTCAAGCC | 7347 |
rs143116314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571519 | TCCACCATACTTTTT[C/G]CCACTGTAACTATCT | 7347 |
rs143189379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597071 | AGAGCAATAATAGGT[A/G]CATTACAAAGATGGA | 7347 |
rs143302082 | in-del | -/TTTATGTA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563126 | GGTACCTCATTATCC[-/TTTATGTA]TGTATGTATGTATGT | 7347 |
rs143472117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565359 | ATTCTGATAGTGTTA[A/C]TTAAAATGTAATTTA | 7347 |
rs143492625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550444 | TGAAATCATCTTCCA[A/G]TCATCTCTTGCCCCA | 7347 |
rs143550807 | in-del | -/T | 0.25634 | 0.24992 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554749 | ACTTGAAACTTTTTT[-/T]GTTTTTTTAAACTTT | 7347 |
rs143559192 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590274 | TAAGATTGCAAGCAT[A/G]TCTCTATGCTTTGCA | 7347 |
rs143580701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583780 | TAGAGATATACTTAC[C/T]GAGATGAATAGAAGC | 7347 |
rs143609331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557375 | TCATTGGACCATAGA[A/T]TAAAAAGAATAAGTT | 7347 |
rs143629592 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589039 | CTAACCTTATCAGAA[-/TT]TTATTTCTCTCCTTA | 7347 |
rs143644841 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588823 | TTATTTCTTCTCACT[A/G]TGATTGTAGTGATTG | 7347 |
rs143669848 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567741 | TTAGTAGAGACAGGG[G/T]TTTGCCATGTTGGTC | 7347 |
rs143717380 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560109 | CAGCATTTTCTGTTG[C/T]TCATACAATGCATTA | 7347 |
rs143795829 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568454 | TGAGAGGTAGATAAA[C/T]ATTAATATTTTTTAG | 7347 |
rs143889899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585823 | TGTTTGAAGGTACTC[C/T]GTAACTAAAGATATA | 7347 |
rs143899351 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570917 | ACCCTGTCTCTATAA[A/T]ATATATATATATATT | 7347 |
rs143941325 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606166 | AAACATTTGTGAAGC[A/G]TCTACTTGTAACGAG | 7347 |
rs144021994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588933 | GGATTACTACTATTA[C/T]GTTATCATACCCTTG | 7347 |
rs144094499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563810 | GTATCAGTGATATTA[C/T]ACAATATTTTTCTTT | 7347 |
rs144098447 | in-del | -/A | 0.5 | 0.00019968 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594590 | ATTCATTTCATTCAG[-/A]TAAGTATGCAATGTG | 7347 |
rs144178661 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548196 | TCCAGCAGAGACTAA[C/G]AGTCTGGCAATGTAA | 7347 |
rs144234355 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556775 | TGGCCAAGTTAGAGA[A/G]TAAAGTACCAAAAAG | 7347 |
rs144287105 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594409 | ACTCAAAGACTGTTT[A/T]CACTGCACTGTTGAA | 7347 |
rs144299419 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561084 | CACAGGCATGTTCCA[C/T]CACACCTAGCTGATG | 7347 |
rs144403522 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600299 | CCGTGAAGGTGGCTA[C/T]GTAAACAACAGATTT | 7347 |
rs144434156 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590535 | TACTTTATTATTATT[A/T]TTTTTTTATGTTTCT | 7347 |
rs144646481 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576260 | TCTGATGTGAAGTCT[C/T]GCTCTGTCTCCCAGG | 7347 |
rs144711975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580335 | CTGAAATTTACTAAA[A/G]AATCTACAGAAATCC | 7347 |
rs144740941 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557552 | CCAGAAGACTGGTGA[G/T]AGAGGTTATGAAACC | 7347 |
rs144840383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558652 | GTATCTTTTCTACTT[A/C]TTTTCCTCATTATAC | 7347 |
rs144907575 | snp | C/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598797 | CAGTTGCTCATCAAG[C/G]TTTTATCCTCCAGAT | 7347 |
rs145008469 | in-del | -/T/TT | 0.00613656 | 0.0550884 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590175 | CAGTGACAAGGGCTG[-/T/TT]TCTTTTTTTTTTTTT | 7347 |
rs145058879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562082 | GATGATTTGTCATAT[C/T]TGTGCTCAGGTCATC | 7347 |
rs145090403 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577764 | AGTCTGCAAGTCAAA[C/T]GTGAAGCCAAGAAAG | 7347 |
rs145119334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601607 | ACATAATGCTAATGT[A/G]TACCTAATAGACTAC | 7347 |
rs145171686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585206 | TACCCTTATCCTCCA[A/G]AAAACAAACACACAT | 7347 |
rs145345649 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591680 | GCACACTGCTCGGGT[G/T]TGAATCCAGATTCTA | 7347 |
rs145352525 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582156 | CATGCTTATGGTCTG[A/T]ATTCTCATAGCTCAC | 7347 |
rs145502012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555685 | CTTTCCCGTAACTTT[C/T]TCCAGTTGTCTATCA | 7347 |
rs145569551 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559178 | CCGAGTAGCTGGGAA[A/T]ACAGGCGCCAGCCAC | 7347 |
rs145662254 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602285 | GATGTTTGTCATGTC[A/G]CTTGTCTCTTGTACA | 7347 |
rs145734815 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550935 | CTTAGGGAGGAAACA[G/T]TTGATCTTTCACCAT | 7347 |
rs145764175 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586288 | GACATTACATAAGGA[C/T]AAAGAGGTTATCTCA | 7347 |
rs145768050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567396 | GTTTTGTCTTGAAAC[C/T]ATAGTTTTGAGCAAT | 7347 |
rs145801862 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549463 | GCGGGTGACCACGCG[C/G]TCCCAGACCGGCGCA | 7347 |
rs146055567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554373 | ATCAAATTACTACAT[A/G]TAAAATATGTAGAAC | 7347 |
rs146075577 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558530 | TAAAATTAACAAATA[A/C]ATTTAAATTCTCTTA | 7347 |
rs146293310 | snp | G/T | 1.72952e-05 | 0.00294063 | stop-gained | UCHL3 | GRCh38.p7 | 13:75560856 | CAGTCTGTGCAGTCT[G/T]ACTTCTCTTTCCTAT | 7347 |
rs146296279 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594648 | AAGTGCTGAGGCTTC[A/T]AAGGTGAACACAATT | 7347 |
rs146314872 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599797 | ACCCTACAAAGGCCT[C/G]TAAGCATTCAAGTCA | 7347 |
rs146315322 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547248 | CATCAAGAGGACTCT[C/T]GTTTCCAGTATAAGA | 7347 |
rs146334240 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553446 | AGCAGCATTTGGTAG[A/G]ATAGCTCACTCCATC | 7347 |
rs146642262 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548221 | ATGTAACTCTAGTGA[C/T]AATGCAACTAAGCCC | 7347 |
rs146744021 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565500 | ACTTGTAGGTTTTCT[A/G]TAGACATCGTTTGTT | 7347 |
rs146762382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571667 | ACCTGAATCAGTTGG[C/T]TGCTAAAATTTTTCT | 7347 |
rs146865307 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585945 | AAAAAGCAGAAAAGT[A/T]ACAGAGCAGATGGAA | 7347 |
rs146883522 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590385 | TGATGAGCACTGATC[C/T]ACATTCATGATAATG | 7347 |
rs146906048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568562 | TCACTTATCAGAAAC[A/G]TATTACATACCAGTA | 7347 |
rs146921651 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593106 | AGATGGTGTTAAGGT[A/G]ACTAATAATTTATGA | 7347 |
rs147010594 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588323 | CACTATTTATTAGTC[A/G]CCTCTCCTTCTATCT | 7347 |
rs147171793 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606198 | TGGATGCCATTCTGG[A/G]TTCAGAAGTTAAAGC | 7347 |
rs147294269 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559968 | TTCCTGTGACATCTT[A/C]AGAATTGTAAAAAAA | 7347 |
rs147399102 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579835 | TAATGTTAGGATATA[A/C]GATTTTTTTGATTTG | 7347 |
rs147415956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583670 | CACATTTTCACTAAA[A/G]CGTAATTGTAGAAAA | 7347 |
rs147488876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584563 | CATTTTTAGGCATAC[A/G]TATTATTTATCACAG | 7347 |
rs147504528 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601122 | ATAAAACTTGAACAA[G/T]TAAGGAGTTGCTTCT | 7347 |
rs147520161 | snp | A/G | 3.30814e-05 | 0.00406689 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605749 | CATAGAAGTTTGCAA[A/G]AAGTTTATGGAGCGC | 7347 |
rs147560816 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596450 | TCTGGGTGGTTGCTG[A/G]AAGCAGATTTTCTAC | 7347 |
rs147577432 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550638 | TTGGGGAGGGAGGAG[A/G]GAACATCTCCCAGCC | 7347 |
rs147593684 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555784 | TCTTTTTGAGATGGA[C/G]GTCACACTATGTTGC | 7347 |
rs147682096 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572986 | GATTCATCTCCCTGC[C/T]GGGCATGGGGGCTCA | 7347 |
rs147698309 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575855 | CTCCCTGGTTCAAGC[A/G]ATTCCCCTGCCTCAG | 7347 |
rs147771446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556852 | ATAGTGTTCAGATCC[C/T]TGCATGTGAGTTCTG | 7347 |
rs147801740 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596132 | CTGTAAATGTGATCC[A/G]TAAAATTTAGGTGGA | 7347 |
rs147892375 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580560 | TTGTCCTCTCCCTCT[A/C]CCTCTCCTCAAAATT | 7347 |
rs147984413 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578129 | ACAGTTGAGATCAAG[C/T]GATTTTATTTGACTT | 7347 |
rs148048350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557460 | TTGGCCAAAATTTTA[A/G]AGGCATTGTGAAAAT | 7347 |
rs148137453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573847 | CTTTGTGCTTTCTAA[C/T]AACCCAGTACACTTC | 7347 |
rs148195198 | in-del | -/TG/TGTG/TGTGTG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563920 | GCCGAATAATATTTC[-/TG/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 7347 |
rs148260299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597077 | ATAATAGGTACATTA[C/T]AAAGATGGACAGTTG | 7347 |
rs148280476 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582957 | CAACTCTTTGAAATT[G/T]AAAATATATATGATG | 7347 |
rs148312597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562489 | ACAAAAATAAGCCAA[C/T]AGATAACTATTCCAG | 7347 |
rs148420292 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564396 | ACCTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 7347 |
rs148551570 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582530 | AATAATTGTTAGTGA[-/T]TTTTGGACTCTTCAC | 7347 |
rs148665619 | snp | A/C | 0.0107286 | 0.0724924 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575820 | GCAGTGGCATGATCT[A/C]GGCTCACTGCAACCT | 7347 |
rs148787704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600570 | GATGATAGTATATCT[A/G]TTTATAGCCTGGATT | 7347 |
rs148804591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554419 | GCATGCTCTCCATGA[A/G]TGTCGGCTATTTTTA | 7347 |
rs148809111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585788 | GAGGTTCTTATACTA[C/T]ATATGTAGTGGTGTA | 7347 |
rs148862350 | snp | A/G | 0.00214573 | 0.0326843 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549815 | GGAGGGCCGGGCACC[A/G]CGGCCATGGAGGGTC | 7347 |
rs148897808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602386 | TAGTTACTACCAAAA[A/G]GTCAGGCCACTATTT | 7347 |
rs148914021 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556862 | GATCCTTGCATGTGA[A/G]TTCTGGCAGGTGGCC | 7347 |
rs148929423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580863 | ACGTGTAGGTAATAC[A/C]AATTGCTGAAACTAA | 7347 |
rs148950521 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567586 | GCAGTCTCGCTCTGC[C/T]GCCCAGGCTGGAGTG | 7347 |
rs149070257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591883 | TTTATATTAGACTTA[C/T]CTGGTTGAGTATCTC | 7347 |
rs149197479 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577498 | GGATTTTGGTGTCTT[C/T]AGGGGGGTCCTGAAA | 7347 |
rs149235947 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554531 | ATTCCAAATATGGCT[-/A]ATTCCATTTCAGCTG | 7347 |
rs149286427 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593876 | TACTTGAAAATATAT[A/T]CTTACTTGAGGATGA | 7347 |
rs149339495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558560 | ATCAGGGTTCATGAT[A/C]CTTTTCCTTAAAAGG | 7347 |
rs149425413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573518 | GCAAAGTGTCAGCAG[G/T]GTTGGCTTCTACTGA | 7347 |
rs149430033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605583 | TAGGGCACCCATGTT[C/T]ACTTTTCTGGTGTTC | 7347 |
rs149462577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582616 | CTCTCTTTAAGACTT[G/T]TATGAAAGATTCAAA | 7347 |
rs149483345 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570689 | TAAAGCAGAAGGATC[A/G]CTTGAGGCCAGGAGT | 7347 |
rs149500047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553342 | TGTGTGTACCATTTC[A/G]TAGTAACTTTTTTTG | 7347 |
rs149550685 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599916 | CTCTTGTGCAAAACA[A/G]TAAGCCAAGTTGTGA | 7347 |
rs149695719 | in-del | -/GGCGGCGGCGGCGAA | 0.357271 | 0.225816 | intron-variant, upstream-variant-2KB, cds-indel | UCHL3, COMMD6 | GRCh38.p7 | 13:75549766 | CGCGTGGGCGGAAGC[-/GGCGGCGGCGGCGAA]GGCGGCGGCTGTCAG | 7347 |
rs149728342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579209 | GGAAGAAGCTTAGTT[C/G]TTAAATAATATAAAA | 7347 |
rs149817238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75595947 | TCCATAAGACCTTCT[C/T]GAGTTTTAAAAAAGC | 7347 |
rs149834078 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549182 | TGAACTCAACTTTGT[A/G]TCAATACTTAGTACA | 7347 |
rs149871096 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561611 | TGATAATGTAGGTTA[C/T]ATTATTTTCAAAATA | 7347 |
rs149956085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575513 | TGTTATTAGAGTTGC[C/T]ACAGAAGTTTGATAT | 7347 |
rs150097175 | in-del | -/T | 0.181978 | 0.240568 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553645 | CCTAGTAATGTTTTC[-/T]GTTGTATAGTTCTAA | 7347 |
rs150100553 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587890 | GTAAACCAGTGGTTT[C/G]CCCCAGCTCAGTATT | 7347 |
rs150346500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598540 | TGCTTTCTTGTCTTT[C/T]ATGACTGTAACATTT | 7347 |
rs150363011 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552823 | TTATTATTTATGACC[A/G]TACTAAATCTTCATT | 7347 |
rs150420250 | in-del | -/GTCTTGTCTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571978 | GTTTTCCTAACCCTG[-/GTCTTGTCTT]TCTTGTCTTGTCTTG | 7347 |
rs150432201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572655 | ACTGTCCTTGGTAGT[C/G]TAAGAAATAAAAAAA | 7347 |
rs150595473 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578740 | ATTAATATGTAATCT[A/C]TTTTGGTTAGTGTTG | 7347 |
rs150625029 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589825 | AGATAGATTATGGTT[A/G]TTAAAAATAGTAGAC | 7347 |
rs150677527 | snp | A/G | 3.30814e-05 | 0.00406689 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605748 | CCATAGAAGTTTGCA[A/G]GAAGTTTATGGAGCG | 7347 |
rs150682636 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595384 | AGGCGGATAACCTGA[A/G]CTCAGGAGTTCAAGA | 7347 |
rs150814669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563500 | TGGTGGGTTTTTAAA[A/G]ATAAATTTTATTGTG | 7347 |
rs150873840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569965 | TTTACCATCTTTACC[C/T]TGTTAGCTAGTTCAG | 7347 |
rs150888552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555362 | CTTGTTTATGTGTAT[A/G]CTTGTTTATCATGTG | 7347 |
rs150925870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564617 | TTCCCACCAACAGTG[C/T]ACTTGGGTTCCCTTT | 7347 |
rs150967301 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586381 | TAAATGTATGAGGCA[A/G]ACACTGTTAGAACTG | 7347 |
rs150977638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572431 | CATAGTTTACTTGGC[A/G]TTATTCCCATCTTAG | 7347 |
rs151120515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581209 | ATGGTTATAAGGATA[C/T]TTTTCATAATAATAG | 7347 |
rs151126090 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595269 | AACTGCTTCAAATCT[C/T]TCTGGCAATCATTAC | 7347 |
rs151157498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591955 | TCCTTTGAACATCCT[C/G]TTGGTGCTCAAAAAG | 7347 |
rs151159240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561134 | GAGACAGGGCCTCAC[C/T]GTGTTGCCTGGTCTG | 7347 |
rs180783831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575424 | TAGTGGCAGAGAGTG[C/T]TTTCTTTTTTTCCAT | 7347 |
rs180785358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553937 | TCAGATTGCCATTCC[A/T]GAGAGGCCGTAGTAT | 7347 |
rs180810567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595066 | TGATAAACAGGACTA[C/T]TGATATTTATTGTGT | 7347 |
rs181016696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590690 | TACTTGGTTTAATCT[C/T]GATCTGATCTTTCCT | 7347 |
rs181016902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570095 | CCTGACTGTATCACT[C/G]TAAGAGGAAGTTTGT | 7347 |
rs181045133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599274 | CTGCACACAGGCCAT[A/G]GTTTTAATTTTTAAG | 7347 |
rs181122557 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574858 | TTTTTTGGGTCATAT[A/G]TGTAGGAGTCTAGAG | 7347 |
rs181122866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552402 | TCACTCTGTTACCAT[C/T]TGGTAATTGCATGTG | 7347 |
rs181125614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594697 | GAGATTAAGAAAGTT[A/G]TGCTTTTAGTCACTG | 7347 |
rs181332258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557173 | TGAGCTGTGATTGTT[C/G]TCACTGCACTCCAGC | 7347 |
rs181353400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569214 | CCCTACTTAGAGCCT[A/G]GAAATTACAAATAAT | 7347 |
rs181354146 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548241 | CAACTAAGCCCATCA[C/T]GAGCTGGACACTGCC | 7347 |
rs181454602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558711 | CAGATGGCTAGGTTA[C/T]CTACTAAAGTAGAGA | 7347 |
rs181467370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589659 | TTTTAGTGGCTTTTA[C/T]ATATTAATTTCCATG | 7347 |
rs181492160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599424 | ACTTTACATATATTT[C/T]ATTTTTTACAAATTG | 7347 |
rs181494317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580562 | GTCCTCTCCCTCTCC[C/G]TCTCCTCAAAATTGT | 7347 |
rs181640753 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588877 | TTTTTTATTTTATAT[A/T]CTGGTGTTATTAATC | 7347 |
rs181705123 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547915 | TCAACACATTTATTG[C/G]GTGGTATGGAAAGCT | 7347 |
rs181754699 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568099 | ATTTAATTCAGATGA[C/T]AGTGATTTTACCACT | 7347 |
rs181887128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563033 | GCTGCAAAGTGTTTG[C/T]CTTTGAAGTTCCAAT | 7347 |
rs181912309 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562844 | GAAAATGATGTAAGT[A/C]AATATATAAGTAAGC | 7347 |
rs181942649 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557596 | GATGTAAATGGGATG[C/T]TTCTAATTAACTGTG | 7347 |
rs181945499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604599 | TTCTAACTAATAACC[C/T]TTAATAAAAAATATT | 7347 |
rs181952301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582865 | TGAATTTTACGTTTC[C/T]ATAATAGCACACTTT | 7347 |
rs182084467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597531 | AAAAAACAAATTTTG[A/G]AAACAACATAACAAC | 7347 |
rs182103240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578225 | TTGCTACTGTATACT[A/G]TCATGTGAGTAAACC | 7347 |
rs182159913 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583527 | AAGATCTGTAGCATC[A/T]ATAGTTTAGAACATC | 7347 |
rs182198937 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576325 | ACGTCTGCCTCCCAG[G/T]TTCAAGCAATTCTCC | 7347 |
rs182221578 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580513 | TCCCAATTATTTTCT[A/T]TTCCATGTGCCATAT | 7347 |
rs182407254 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595833 | GACTATTTCATGGCA[C/T]GTTGGAGGAGATCAC | 7347 |
rs182472167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554569 | GCAAGCCACCATCCT[C/T]AGCTTGGACAACTAT | 7347 |
rs182501890 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584029 | TGCTGTGGGAAAGGC[A/C/G]TGAAGCCTGGATTCT | 7347 |
rs182506064 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555787 | TTTTGAGATGGAGGT[A/C]ACACTATGTTGCCCA | 7347 |
rs182527343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599820 | TCAAGTCACACGTCT[C/T]TCACTTTAAGTCAAA | 7347 |
rs182532302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571489 | CCCTTTATTGTTTCT[A/G]TTTCTTACAATAGTT | 7347 |
rs182533712 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550300 | CTTCGTTTTGCCTCC[G/T]GTTAGTGCCGATTCC | 7347 |
rs182538025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580743 | GATCCTCTCAACTCC[A/G]TAAGATAGCTGTTAC | 7347 |
rs182753868 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601303 | ACAACATTTTTGGAA[G/T]AAGTTCTCCTGTGGG | 7347 |
rs182769037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560503 | CTACCATTCTGCCCC[C/T]CTAGTTTTACTGAAG | 7347 |
rs182770749 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563822 | TTATACAATATTTTT[A/C]TTTCTGTGTCTGGCT | 7347 |
rs182912983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581755 | CAGCATTTCAAATAC[G/T]TTGGTTATTTTATTT | 7347 |
rs182916854 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561311 | ATGATCCCCTTCTTG[A/C]ATAAAATTAGGCAAT | 7347 |
rs182938648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601651 | CATAACTTTTATATG[C/T]ACTAGGAAACAAAAA | 7347 |
rs183025211 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555626 | TTTTATTATAATAAT[A/G]TATAAGTAGAAGAAT | 7347 |
rs183029024 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581019 | TTGTTCTTTTTTGCC[A/G]TTAACATCTAAGTCA | 7347 |
rs183059182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596452 | TGGGTGGTTGCTGGA[A/C]GCAGATTTTCTACTC | 7347 |
rs183301636 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592172 | TTATATCTAATTGAT[A/T]TGTTATCACTTTTTA | 7347 |
rs183348122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559723 | GTTTTTAATTTCAAA[A/C]TTTCAGATGTTAGAC | 7347 |
rs183379474 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585213 | ATCCTCCAAAAAACA[A/C]ACACACATATATACC | 7347 |
rs183386770 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564391 | TCCTGACCTCGTGAT[C/T]CACCCGCCTTGGCCT | 7347 |
rs183497218 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566423 | AAAATGTTAATACAT[A/C]TTGCCATATGCCCTG | 7347 |
rs183589267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570823 | AGGCTGAGGTGGGAG[A/G]ATTACTTGAGCTCAG | 7347 |
rs183612785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75598980 | AATGATTATAATCCA[C/T]GATATCATGTATTTT | 7347 |
rs183625441 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565303 | CATACTGAACCTTTC[C/T]AGTTTTTTATCAATC | 7347 |
rs183729832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592772 | TTTTTAGAATTTTGT[A/G]TTTTTAGTATGCACT | 7347 |
rs183732548 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573092 | CAACATGGTGAACCC[C/T]GTCTCTACTAAAAAT | 7347 |
rs183773865 | snp | A/C | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550845 | TCACCGTGTTCTTAA[A/C]AATATTGGTTTTTGG | 7347 |
rs183783926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586000 | TTTAAATCCAGCCAT[A/G]TAAAACATCACATGA | 7347 |
rs184090463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598192 | TTACAGAAATAGTAT[A/G]CAGAGCTCCCATACA | 7347 |
rs184135882 | snp | A/C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574880 | AGTCTAGAGCTCAGG[A/C/T]GAGATATCTGGAGTC | 7347 |
rs184136173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594724 | ACTGTTTTCTTTGCC[A/G]ATAACTGAGCACATT | 7347 |
rs184147722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552507 | CACATGTCTACTATA[G/T]GCAGATGAGTATTAA | 7347 |
rs184199016 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587761 | AAGAAGAGGGCCATC[A/T]TACCTGAAGTTGGAA | 7347 |
rs184204358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557519 | TTATTTTATTACTCA[A/G]TATTTAAGTTTGAAA | 7347 |
rs184328456 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579670 | GGAAAATTCTTAGAC[C/G]GAACTTACCAGTTCA | 7347 |
rs184448872 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562388 | CACAATGGTAAGGTT[A/T]TGATTACTGACATTT | 7347 |
rs184495721 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75604196 | TGAGTTTAAATAATT[C/G]TGGACTTCTTAAAAA | 7347 |
rs184620449 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582523 | ATGAAATAAATAATT[A/G]TTAGTGATTTTGGAC | 7347 |
rs184636351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598612 | AATTTAGGCCATCTG[A/G]TTTATCCTCATGATT | 7347 |
rs184638337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579143 | TATTTATTTCCCTCC[G/T]TTTGGAATTTATTTC | 7347 |
rs184645699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556757 | ACTCTCAGGAGTTCA[C/T]TGTGGCCAAGTTAGA | 7347 |
rs184676792 | snp | A/G | 1.67846e-05 | 0.0028969 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567192 | CTCTCTGCTGTATCA[A/G]GCCTTTTTAATTTTA | 7347 |
rs184678787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588633 | TTTTTAAAGGTTAGT[A/G]TATTGTATATTTAGA | 7347 |
rs184739072 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547684 | ACCATATAAACCAGA[C/T]GGTGGAAGTTAAAAT | 7347 |
rs184797987 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582356 | GCCTAGTCTAGGTTT[C/T]TTTGAACTATAATGA | 7347 |
rs184858414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603364 | GCCAGGTGCTGTTGC[A/G]TGTGCCTGCAGTCCC | 7347 |
rs184918778 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561796 | GTGTGTGTGTATATA[C/T]GTATACGTATACATA | 7347 |
rs185027803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551495 | CCTGACGCCAAACTA[A/G]ACAATTCATATTAAG | 7347 |
rs185049438 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593611 | GGAGCAACAATAAAA[C/T]TAGATAACTCTGATT | 7347 |
rs185131591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569334 | TAGTACTAAGCTTTT[C/G]TTAAATTTCCTTCAA | 7347 |
rs185133587 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548596 | TGCCTTTCTCCGTGG[C/G]TACTGTTTTAATTTT | 7347 |
rs185171757 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574681 | CAATAAATATTAGGC[A/G]GTAATTTTATTTTAC | 7347 |
rs185316046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568261 | CAAATTATTTGGTTA[A/G]AACAATGCCTTATGT | 7347 |
rs185365239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584335 | AGGCATAGCCTCTGA[C/G]CAAAAGCCTAAAGCT | 7347 |
rs185377794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564029 | GATAGGATTGGGTAC[A/C]TTCAGGGTACTATGG | 7347 |
rs185379521 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595191 | AAGCAACTTATAATT[A/C]AAAAATGTTTGCATA | 7347 |
rs185415327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589018 | TGAAAAGGTGTTCCC[A/C]AAATACCTAACCTTA | 7347 |
rs185595636 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578612 | TCTAAATTTTTGCTT[C/G]TTTAATAGGGGGAAA | 7347 |
rs185671169 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604948 | ATCCTTGTTCTCTCT[A/T]GAAAATCCAAAAAGA | 7347 |
rs185692489 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583230 | TTTAAAAATAAACAA[C/T]TACAATATATTGATA | 7347 |
rs185731209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556200 | TTGTAGTTAGTCCAT[A/G]TTGAGCCTGCAGTGA | 7347 |
rs185748683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562996 | AAAGTTATTAAGAGG[A/C]TATCTAGTGCATTCT | 7347 |
rs185790811 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600451 | GCAGACGGTGACTTT[C/T]AGTTGAAGCCAATGA | 7347 |
rs185801041 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559750 | AGACCAGCAAATACT[A/G]TAATGTGTTCTTGAG | 7347 |
rs185921434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599525 | GTGTTTCTGTGTCAC[A/G]CTTTGGTAATTCTCC | 7347 |
rs185926500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580780 | TTGCAGATGGGAAAT[C/G]TAAGAAGCTGCTAAT | 7347 |
rs185939544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580622 | TCACCTTCTTAATTC[G/T]TACTCCTTTTGAAAG | 7347 |
rs185989728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559061 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTGGCTCTG | 7347 |
rs186227720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554100 | TCTTGTTCTATCTCC[C/G]AGGCAGGCTGGATTA | 7347 |
rs186342321 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583806 | GAAGCCCAAAATTTA[A/G/T]GGGTAATGAAACAAA | 7347 |
rs186424815 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591510 | TTATTTCTTTTCTAC[C/T]TAAAAATGTTCCAAA | 7347 |
rs186427829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570381 | GCTGGAACTACAGGC[A/G]CCCGCCACCATGCCT | 7347 |
rs186493921 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550524 | AAAGCTGGACATTTA[A/C/G]TTGCTGTTGTATCAA | 7347 |
rs186534315 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605281 | GGGAGGCCGAGGCGG[A/G]TGGATCACCTGAGGT | 7347 |
rs186542575 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554670 | AGTGGCCTTAAATAA[A/T]TGAGAATCACATCTT | 7347 |
rs186552269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563078 | TGTAGTTGTGAATGA[C/G]TTAAGCATACTAATA | 7347 |
rs186588118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596248 | ATAGTATTTATAAAA[A/G]TGTGCAACCCTGAGC | 7347 |
rs186678477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587881 | CTGCTTGCTGTAAAC[C/T]AGTGGTTTCCCCCAG | 7347 |
rs186771907 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576390 | ACGTGCCACCACACC[C/T]GGCTAATTTTTTGTA | 7347 |
rs186931228 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596557 | TAACTTCAAGAAAGT[A/C]GATTTGGCCAGAGCA | 7347 |
rs186932818 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576917 | TTGGCCCGCTGTAAT[G/T]GTGGGTTCCTTACTT | 7347 |
rs186988871 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555629 | TATTATAATAATATA[C/T]AAGTAGAAGAATTAT | 7347 |
rs187076236 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548180 | CCTGGCATGCACTGA[A/G]TCCAGCAGAGACTAA | 7347 |
rs187171023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572721 | GTAGTCCCCCGAGTA[A/G]ACAAAACATATCCAT | 7347 |
rs187172727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592627 | TAAATAATTACAGAT[A/T]TTTAGACTCTGAGAC | 7347 |
rs187174652 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549270 | GCTGCCTCCCGCAAG[A/T]GCAGACAAGGCCAAC | 7347 |
rs187176634 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580515 | CCAATTATTTTCTTT[G/T]CCATGTGCCATATTT | 7347 |
rs187347531 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557679 | GGAAAAATATTTTTG[G/T]TATAGTTTTAAGACC | 7347 |
rs187379636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564397 | CCTCGTGATCCACCC[G/T]CCTTGGCCTCCCAAA | 7347 |
rs187380755 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585338 | AGAGTAGATACTAAG[A/C]ATTCATAAGAATTAC | 7347 |
rs187383442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599316 | TCTCTGAGTTTGCAT[A/G]GCATTTGAAAATATG | 7347 |
rs187526747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601737 | ACCCACAGTATCTCT[C/G]AGGCATGCCTGTACA | 7347 |
rs187583336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582023 | AGTGACCTTGCAATG[A/G]AAAACACTGAAATTG | 7347 |
rs187596897 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561552 | TTTCAATATATATAT[A/G]TATAAGGAATCTTCT | 7347 |
rs187670008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578385 | TACTGATTCAAAGGG[A/G]TAAATATTTTTATGA | 7347 |
rs187697958 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592983 | TACAGGGATTGGGTC[C/G]ATATTCAGTTCTCTG | 7347 |
rs187819615 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560539 | TTGACAAAAATTGAA[C/T]ATATTTAGAGTGTGC | 7347 |
rs187918986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556100 | TCTGCTGAGTAATCT[A/G]TGTCGAGTACAGTGG | 7347 |
rs187922076 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586138 | AAGTCATTTTAAAAA[A/G]CGTAAGAAGATAACA | 7347 |
rs187944941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597547 | AAACAACATAACAAC[A/T]ATTTACATAGCATTT | 7347 |
rs188064787 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556358 | TAACTAATAGTTATT[C/T]TACTTCTACATTTAG | 7347 |
rs188175793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565316 | TCCAGTTTTTTATCA[A/G]TCGAACTTACATGAA | 7347 |
rs188232455 | snp | A/G | 0.000139748 | 0.00835789 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566652 | TGAGTTTTTTAATAT[A/G]TTATTTTCCACAAAT | 7347 |
rs188427737 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570903 | GGGGACAGAGCAGGA[C/T]CCTGTCTCTATAAAA | 7347 |
rs188547964 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598873 | TGCCAAATGGCAATT[A/T]AAAAAAAATTCCCCC | 7347 |
rs188615177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579269 | AGGCGGAAACAATAC[A/G]TGTATCATGCGGTTC | 7347 |
rs188617331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557041 | GGCAACATAGTGAGA[C/T]GTCTCTACTAAAAAA | 7347 |
rs188677141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550928 | TCTCTATCTTAGGGA[G/T]GAAACATTTGATCTT | 7347 |
rs188685197 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581270 | CTGTAAACCAAAACC[C/T]ACTTACTTTATTTTA | 7347 |
rs188725910 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550108 | TTTCTTGAGGGCCCC[A/T]CTTGTTCGGCTTTAC | 7347 |
rs188748352 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592330 | ACAAGAATAGTCATA[C/T]TACATCTATGAAGTG | 7347 |
rs188855227 | snp | A/T | 8.24463e-05 | 0.00642 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75594944 | TGAGAAAGTAGATCT[A/T]CATTTTATTGCATTA | 7347 |
rs188857252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575334 | CACTGAAAGGTATTG[C/T]TTTCATCTTTCGCTT | 7347 |
rs188871374 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553314 | CCTTATTCATTCCTG[C/T]GTAGCTTGCTTCTGT | 7347 |
rs188936437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598407 | ATCTGATCCACAGAC[C/T]CCATTACAGTTTTCC | 7347 |
rs188961764 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601493 | AAAGCAAGCCCCTCC[A/T]TCAGCAAAAAGATGG | 7347 |
rs188964137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604980 | AATTTATATTAGTGT[C/T]AAAAATCTACAACAA | 7347 |
rs188982613 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563004 | TAAGAGGATATCTAG[C/T]GCATTCTTTAGGAGC | 7347 |
rs188984754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583253 | TATTGATATGCTATC[A/C]TATTTTGAATGTTGT | 7347 |
rs189003354 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573747 | ACTTCCTTCAATGCC[A/T]AGTTTTCAAATATAG | 7347 |
rs189175521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580337 | GAAATTTACTAAAAA[A/T]TCTACAGAAATCCAT | 7347 |
rs189195611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582811 | TTTAAAAGTTGGTGT[A/G]TGTATCTTTAATCTT | 7347 |
rs189214182 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578644 | AACATGTTTGATTGC[C/T]AATGATACTTAAAAG | 7347 |
rs189254123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562801 | GTTCTAAAGTATTTG[C/T]GTAAGTAAATTTGTA | 7347 |
rs189424080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589352 | TTATATTTAATGATA[C/T]TGTTTCCTAAAAGAT | 7347 |
rs189442976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580540 | ATATTTTAGACTCAG[C/T]GGTCTTGTCCTCTCC | 7347 |
rs189464356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557581 | CCTTTTATCCTGCTT[C/G]ATGTAAATGGGATGC | 7347 |
rs189495175 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599057 | AACTGCAGCCTTGAT[G/T]TCCTGGGCTCCAGCA | 7347 |
rs189499910 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548200 | GCAGAGACTAAGAGT[C/T]TGGCAATGTAACTCT | 7347 |
rs189506395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558211 | AAAAGCATGATTCTG[C/G]TTAAAATTTAATCAA | 7347 |
rs189515388 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588758 | TATTATGGTTGTTAC[A/G]GTTAGCAAAATCTAT | 7347 |
rs189708953 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568359 | TTTAAATTGTTTTTT[C/T]CTTTAAAAAAAAACT | 7347 |
rs189753240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561831 | TACGTATATACGTAC[A/G]TATATACGTATACGT | 7347 |
rs189789383 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603999 | TTCATTCATTTTTTT[A/T]AAAAAAATCTAACAA | 7347 |
rs189878985 | snp | C/T | 0.000297113 | 0.0121848 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569442 | TTTTTCCAATGAATA[C/T]CTTTATTCTTATTAC | 7347 |
rs189881119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590464 | AGCTTTCTGAATTCA[G/T]TTAGTTGACTCAGGT | 7347 |
rs189897718 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548672 | TGTTTCTGCATATCT[A/G]ATCATCCCATTTATT | 7347 |
rs189989384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599567 | ACGTTTTATTATTAT[A/G]TCTGTTATGGTATCT | 7347 |
rs189993642 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550136 | TACGCGGGTCCGCCC[A/C/G]TTTCAGAAAGGGCCA | 7347 |
rs189997654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580719 | TAAGTGCTGTATCTA[C/T]CCTAGTTTGATCCTC | 7347 |
rs190000051 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582438 | CTGTTGCAGTGCCCA[C/G]ATAGTCAGCAGTGAG | 7347 |
rs190003122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574805 | GAACCACCAAAGATG[A/G]TACATTTACTTTTCA | 7347 |
rs190204462 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555716 | TTCTCATTGAAACCA[C/T]AGAGTAAATCTAATT | 7347 |
rs190233621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597455 | TCTGTGGGTTCTTGC[A/G]TTGGTAGATTCAACC | 7347 |
rs190250296 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577379 | ACATTTACATTGTAT[C/T]AGGTATTACAAGTAA | 7347 |
rs190251326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594004 | TTTAAAATTTGTGCT[C/T]TATTTGCATTTTTAA | 7347 |
rs190261329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551655 | AAAGCTGGTTCACCA[C/T]TCAAAAATCAATGTA | 7347 |
rs190506656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599332 | GCATTTGAAAATATG[A/G]CATTCTGTTCTTTTA | 7347 |
rs190537243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555592 | TGAGCAGCATTCTAT[C/T]TCTTAAAGTGGTTTA | 7347 |
rs190581811 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568003 | GCAAAGGTTTAAAGG[C/T]AGACATTAGACCATA | 7347 |
rs190749910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580881 | TTGCTGAAACTAAAT[A/G]AAATGAGGTTTTTAA | 7347 |
rs190788091 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547748 | TTTGTAAGGGTTTTA[C/T]GGGTCTAAAGGTCTG | 7347 |
rs190920654 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585119 | GAAGGGTAATGGCCA[A/G]CTATTTTCCAAAAAT | 7347 |
rs190924612 | snp | C/T | 0.040671 | 0.13668 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564273 | CTCCCACCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 7347 |
rs190990792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600626 | AGACGTACTGCTCAG[A/T]AAAAGATTCCTTTGA | 7347 |
rs190993881 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592428 | TTCATATATATATAT[A/G]TATATATATATATAT | 7347 |
rs191000048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560218 | CATTTTTGGTAAATA[A/G]GATAAACTATGTTGA | 7347 |
rs191243255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550707 | TCTGCTCAGGTGTGC[C/G]TTATTTTACCCTGTT | 7347 |
rs191279056 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592691 | CAGGTTCTGAGGTTT[C/T]GTGGAAGGCTTAGAA | 7347 |
rs191279201 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572818 | ACTGTTTTGTGCACT[C/T]CAGGGTGGAATATAC | 7347 |
rs191304710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571357 | TTTTTCAGACCTAAC[C/T]GCCTTCATTCTTTCC | 7347 |
rs191309191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563749 | TACATCACATCACAT[C/T]CCTGCTAACCTCTGT | 7347 |
rs191527354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583945 | ACCTCAATGGGTGCT[C/T]ATGAGATTAAGTGGG | 7347 |
rs191610995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576412 | TTTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC | 7347 |
rs191617777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582086 | CACACTCACTAGTTA[C/T]GTGGCTTTGGGCAAG | 7347 |
rs191644406 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602434 | GGAAGTGGCACAGCC[C/G/T]GTTTGGACTGGGGTT | 7347 |
rs191811662 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596346 | TAGTATATAATGGAC[C/T]TCCAGGACAGTTTTG | 7347 |
rs191825477 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579395 | ATGACTTAATCTTTT[A/G]GAGGCGATTTTATTT | 7347 |
rs191849076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554469 | TCAGATCTAATTGAT[C/T]TGCAACTCTTATGGA | 7347 |
rs191856238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598904 | AACATTAGAAGCTTT[C/T]CTTTTCCTCTCATTT | 7347 |
rs191870599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595214 | TTTGCATACCATCTT[C/T]GCATTTTAGCAAAGC | 7347 |
rs192116480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585782 | TGTTGTGAGGTTCTT[A/C]TACTACATATGTAGT | 7347 |
rs192137555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576217 | TCCTGAATTTTATTT[C/T]TTTTTTCTTTTTCAT | 7347 |
rs192141098 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578745 | TATGTAATCTATTTT[A/G]GTTAGTGTTGACCTA | 7347 |
rs192241000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582475 | GGTTCACTGTTAATG[C/T]CCTGGCAAACATTGG | 7347 |
rs192302910 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567120 | ATTTCTAACCTACCA[A/G]TGAAAGAATTTAACC | 7347 |
rs192346548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588055 | TGACCCAGGCATCTC[A/C]TGCCTTTTGCCAATA | 7347 |
rs192416535 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549680 | AAGAGGGTGAGAGGC[C/T]CGTCAAACTCTTTTT | 7347 |
rs192446556 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591527 | AAAAATGTTCCAAAT[A/G]TAAATGAACATATAA | 7347 |
rs192531275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561700 | TGGGGATTATAAATA[G/T]CTGTTCTTTGAGCTC | 7347 |
rs192570613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601625 | CCTAATAGACTACAG[A/G]GTAATATAAACATAA | 7347 |
rs192624215 | snp | C/T | 1.6671e-05 | 0.00288708 | utr-variant-5-prime, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560791 | TCCTAACTGGCAATT[C/T]GTTGATGTATATGGA | 7347 |
rs192651466 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UCHL3 | GRCh38.p7 | 13:75604172 | TTGTCAGTTGACTTT[G/T]GGTTAGCATGAGTTT | 7347 |
rs192707816 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561869 | CGTATACATATATAC[A/G]TACGTATATACGTAT | 7347 |
rs192766969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565853 | AAACTGAGATACAGA[A/G]ACATTAAATAATTTG | 7347 |
rs192944886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587549 | CATGATATATGTAAC[C/T]TATCTTCAAATGATT | 7347 |
rs193002526 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597784 | GCTGTATGATTGTAG[A/T]CATTGTGCAAGTTAA | 7347 |
rs193012436 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556134 | ATTACATTATCTTAA[A/G]TGATCCTTCTTTTAA | 7347 |
rs193088647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564884 | TATCTTCAGTAGAGA[C/T]GGGGTTTCACCATGT | 7347 |
rs193114578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574428 | CTTGTTTGTCTTGTT[C/T]GCTTTGAATCCCCAA | 7347 |
rs193142586 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598576 | AAGAGTATAGGGCCA[A/G/T]TTACTTTGAGATTAT | 7347 |
rs193207892 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578457 | CAATCAGATAACCTG[C/T]TTGAGCACCTACTGT | 7347 |
rs193266464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593108 | ATGGTGTTAAGGTAA[C/G]TAATAATTTATGAAA | 7347 |
rs193285787 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551346 | TGAGGCAGGAGAATC[G/T]CTTGAACCCGGGAGG | 7347 |
rs199535219 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599153 | TTTTTTTTTTTTTTT[G/T]TAAATTGGGGTCTAG | 7347 |
rs199571230 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552035 | GTAATACATGGAATA[A/G]TGACAGGAGACCTTT | 7347 |
rs199605560 | snp | A/C/T | 0.000286029 | 0.0119558 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549807 | TCAGAGCTGGAGGGC[A/C/T]GGGCACCGCGGCCAT | 7347 |
rs199615940 | in-del | -/TC | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581156 | TAATTATTTTAACTA[-/TC]TACCCACTAATGATC | 7347 |
rs199641193 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592512 | TTTTTTTTTTTTGCC[A/G]TTTGTGTAGTTATTT | 7347 |
rs199684200 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604750 | GCTAAGCATTCAATT[A/G/T]TTTGTCTGTTTTCCA | 7347 |
rs199782321 | in-del | -/TCG | | | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75589944 | ATTATGTAGTCCTCC[-/TCG]CCATCCTCATCACAG | 7347 |
rs199786714 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603685 | AAAAGGATATTTTAA[G/T]AAGACATTTTATGAT | 7347 |
rs199850670 | in-del | -/AAT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552031 | AAATGTAATACATGG[-/AAT]AGTGACAGGAGACCT | 7347 |
rs199898867 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576391 | CGTGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 7347 |
rs199942114 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562535 | AACAGTAAATAATTG[-/A]AAAAAAAAATCAGTT | 7347 |
rs199998558 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586458 | CTCAGAATCAATAAA[A/T]AGATACAGAACATTA | 7347 |
rs200083122 | in-del | -/AGA | 0.102014 | 0.201495 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577897 | TTGAGGAGCCAGCCC[-/AGA]TATGGGTAGAGATCA | 7347 |
rs200250580 | snp | C/G/T | 0.0011113 | 0.0235463 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566870 | AATGATTTTTCATTA[C/G/T]TGCATTTTTTCCCCC | 7347 |
rs200342851 | in-del | -/TATC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557342 | ATTTTAAATATTCTT[-/TATC]TAGTGAAAAATTTGT | 7347 |
rs200389531 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598873 | TGCCAAATGGCAATT[-/A]AAAAAAAATTCCCCC | 7347 |
rs200478502 | snp | C/T | 0.00264011 | 0.0362365 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604741 | GTAAAAACAGCTAAG[C/T]ATTCAATTGTTTGTC | 7347 |
rs200622787 | in-del | -/AT | 0.00953873 | 0.0683987 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552780 | ATCAAGAATTACAAC[-/AT]ATTTATAGAGTGTGA | 7347 |
rs200631129 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574282 | GTAGGTCCTTCTGTA[-/T]TTTTTTTTTATGATA | 7347 |
rs200687621 | snp | A/G | 0.000399281 | 0.0141238 | missense | UCHL3 | GRCh38.p7 | 13:75594930 | GCACCAAGTATAGAT[A/G]AGAAAGTAGATCTTC | 7347 |
rs200732322 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583357 | TTAGACTCATTATCC[-/T]TTTCTTATTCCTTCC | 7347 |
rs200750821 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568337 | CATTCCAATATACTT[G/T]GAGAATTTTAAATTG | 7347 |
rs200810498 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582352 | AAAGCCTAGTCTAGG[-/T]TTTTTTTGAACTATA | 7347 |
rs200831871 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594590 | ATTCATTTCATTCAG[A/G]AAGTATGCAATGTGC | 7347 |
rs200892369 | in-del | -/T | 0.020951 | 0.100183 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605710 | ACTGAAAAATCATAC[-/T]TTTTTTTTTCCTCCA | 7347 |
rs200965579 | snp | C/G | 1.65291e-05 | 0.00287476 | missense | UCHL3 | GRCh38.p7 | 13:75567233 | TATTCTCAGAATCTG[C/G]ATCAACCTTGAAAAA | 7347 |
rs200999755 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568945 | GTACTATAAGAGTGG[-/T]TTTTTTTTTAGTTCA | 7347 |
rs201058985 | in-del | -/CT | 0.0509478 | 0.151255 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602102 | CGACAGAGCGAGACT[-/CT]GTCTCAAAAAAAACA | 7347 |
rs201092998 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552033 | ATGTAATACATGGAA[G/T]AGTGACAGGAGACCT | 7347 |
rs201201825 | in-del | -/AT/TAG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552032 | ATGTAATACATGGAA[-/AT/TAG]TAGTGACAGGAGACC | 7347 |
rs201235372 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603258 | CAGGTGTGAGCCACC[A/C]CACCCAGCCATAACT | 7347 |
rs201269648 | in-del | -/TGG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595528 | CTTGAACACAGGAGG[-/TGG]AGGTTTCAGTGAGCC | 7347 |
rs201375589 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550185 | CCTGAAGATTCTCCC[A/G]CCACTCCTCTGGTCC | 7347 |
rs201396151 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581154 | GTAATTATTTTAACT[-/G]ATCTACCCACTAATG | 7347 |
rs201540176 | snp | C/T | 0.000165066 | 0.00908326 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569440 | ATTTTTTCCAATGAA[C/T]ACCTTTATTCTTATT | 7347 |
rs201586247 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557962 | AGGACATTTTAATGA[-/TT]TTTTTTTTTTTTGAA | 7347 |
rs201672294 | in-del | -/T | 0.0471735 | 0.146155 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570247 | CCACACTTTTTTTTG[-/T]TTTTTTTTGAGACAG | 7347 |
rs201883008 | in-del | -/CA | 0.101301 | 0.200969 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577891 | TATTAATTGAGGAGC[-/CA]GCCCAGATATGGGTA | 7347 |
rs201923490 | snp | C/T | 0.000371701 | 0.0136276 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549806 | GTCAGAGCTGGAGGG[C/T]CGGGCACCGCGGCCA | 7347 |
rs201962508 | snp | A/G | 0.00149939 | 0.0273394 | missense | UCHL3 | GRCh38.p7 | 13:75594922 | TATTCCAGGCACCAA[A/G]TATAGATGAGAAAGT | 7347 |
rs201970343 | snp | A/C | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602108 | AGCGAGACTCTGTCT[A/C]AAAAAAAACAAAAAC | 7347 |
rs202198962 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581055 | ATTCAGTACACTAGA[-/T]TTTTTTTTTCCTATT | 7347 |
rs367630115 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560057 | AGGTTTCATTGTGTA[A/G]TAGAGGCCAGGAAGC | 7347 |
rs367633793 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549512 | CGAGCGCTCGGCAAG[G/T]CTCGGCTCGGAAGAG | 7347 |
rs367636758 | snp | A/C/G | 2.26483e-05 | 0.00336506 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549795 | AGGCGGCGGCTGTCA[A/C/G]AGCTGGAGGGCCGGG | 7347 |
rs367659912 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587997 | AAACGTATTGATGAT[C/G]ATGCTCCTTGCTGTG | 7347 |
rs367918719 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555016 | TTTCTGTTCTTGCAT[C/T]AGTTTGCTAAGGATA | 7347 |
rs367926789 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574182 | GAGATTGTGCCACTG[C/T]ACTCCAGCCTGGGCA | 7347 |
rs368027062 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577402 | ACAAGTAATCTAGAG[-/A]TGATTTAAAGTATAC | 7347 |
rs368115114 | snp | A/C | 0.000413432 | 0.0143717 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569416 | TCATTTAAAAAGTTG[A/C]GTATAGGCATTTTTT | 7347 |
rs368148784 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569797 | TGGCCTGTGTCTTCC[C/T]TATCAGATTCCTGTG | 7347 |
rs368176284 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578468 | CCTGTTTGAGCACCT[A/C]CTGTACTAGGCACTG | 7347 |
rs368185226 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561541 | AAATACAGTTTTTTC[A/T]ATATATATATATATA | 7347 |
rs368336592 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552798 | TTATAGAGTGTGATA[C/T]AGGCAATTATTATTA | 7347 |
rs368398488 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586449 | ATGTCAACACTCAGA[A/T]TCAATAAAAAGATAC | 7347 |
rs368439502 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570435 | TAGAGACGGGGTTTC[C/T]CCGTGTTAGCCAGGA | 7347 |
rs368538583 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565781 | ATCATCTTTCTCCTC[C/T]CCACCTCACCGATTT | 7347 |
rs368587064 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600324 | AGATTTTCCATGTAG[A/C]TGACTAGCCTTCTCT | 7347 |
rs368826511 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550017 | TGTCGCTCGGGACCT[C/T]GGAGTCTTTTCTGTC | 7347 |
rs368942788 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549967 | GCGTGTTCTCTGTTT[A/C]GTTTTCAGGTCACCA | 7347 |
rs368960445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573961 | GGTGGCTCACGCCTG[C/T]AATCCCAGTACTTTG | 7347 |
rs369025657 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594601 | TTCAGTAAGTATGCA[A/G]TGTGCATATACTGTA | 7347 |
rs369034597 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586454 | AACACTCAGAATCAA[C/T]AAAAAGATACAGAAC | 7347 |
rs369104383 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558489 | CGTGTTTTATAACTT[C/T]ATAACAGGATGACTT | 7347 |
rs369120684 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577969 | GCCCAGAACCCCCCC[-/C]ATGTAAATTAATAAT | 7347 |
rs369219355 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579667 | AAAGGAAAATTCTTA[A/G]ACCGAACTTACCAGT | 7347 |
rs369233893 | snp | A/G | 0.000398857 | 0.0141163 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560921 | TTTCTGGTAAATACA[A/G]TTTTTGTTTTATTCT | 7347 |
rs369238708 | snp | A/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549724 | TCCTCCTCCGGGCGG[A/T]GTGTTGGGAGGGCCC | 7347 |
rs369262388 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592449 | ATATATATATATATA[C/T]ATATATATATATATA | 7347 |
rs369265519 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560992 | CTGGAGTGCAGAGGT[A/G]TAATCATGGCTTACT | 7347 |
rs369304549 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588757 | CTATTATGGTTGTTA[C/T]GGTTAGCAAAATCTA | 7347 |
rs369451272 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571060 | TAATGAAATGCTGTT[C/T]TGTATTGCTTTATAT | 7347 |
rs369579820 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602589 | ACGCAAAGTTGTTGG[C/T]AAGTGACAGTTTTGT | 7347 |
rs369583690 | snp | C/T | 4.99563e-05 | 0.00499756 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604838 | TAGAGGTAACAGTAA[C/T]ACTTGTTGGCCCATC | 7347 |
rs369614682 | snp | C/T | | | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590079 | CCATCTCTCCGTCTT[C/T]GTCGCTGGCGACCCT | 7347 |
rs369663398 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557963 | GGACATTTTAATGAT[A/T]TTTTTTTTTTTTGAA | 7347 |
rs369761273 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571829 | CCCACAGTTTAGAAA[A/C]ACTACTGGAGTGAGC | 7347 |
rs369807222 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579058 | TTTTATTATTTTGGG[A/T]TTACAAAGAGATAAC | 7347 |
rs369867256 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585531 | GGAATTTCATTATGC[-/T]GAAACAGTACAATGC | 7347 |
rs369899006 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600970 | AGTTTGGAATAAGTT[G/T]GTTCCAATCCTCATG | 7347 |
rs369900073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582928 | TTGCTTGAAAGTCTT[C/T]TTCTGAATTAGATCA | 7347 |
rs369920058 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594733 | TTTGCCGATAACTGA[A/G]CACATTGTCACAAAC | 7347 |
rs370104195 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576268 | GAAGTCTCGCTCTGT[A/C]TCCCAGGCTGGAGTG | 7347 |
rs370180562 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572647 | AGCTCAGAACTGTCC[G/T]TGGTAGTGTAAGAAA | 7347 |
rs370182221 | snp | C/T | 6.59185e-05 | 0.00574064 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567329 | TCGGTACCTTCTTTC[C/T]GTTTTGATCTCATGT | 7347 |
rs370281847 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548251 | CATCACGAGCTGGAC[A/C]CTGCCAGTTTTACCA | 7347 |
rs370422978 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573627 | GGGTGTGGAGAGAGA[C/T]GGGGAGAGAGAGATC | 7347 |
rs370501104 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568578 | TATTACATACCAGTA[A/T]GTATATATTTGATAT | 7347 |
rs370698970 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573208 | GGCGGAGGTTGCAGT[A/G]AGCCGATATCCCACC | 7347 |
rs370771567 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75598946 | ATCAGAATGGACTCA[C/T]GGATTCCTACTTTAC | 7347 |
rs370778850 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549504 | GTAGAACGCGAGCGC[A/T]CGGCAAGGCTCGGCT | 7347 |
rs370829699 | in-del | -/ATA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555618 | TTTAATTTTTTATTA[-/ATA]TAATAATATATAAGT | 7347 |