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 |