SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs370897793 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579924 | GAATTAGTTTGAGAA[A/G]TTTAACAATGGTAAG | 7347 |
rs370968930 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570074 | CTTTCTTTCCTTCCC[C/T]CCAGCCCTGACTGTA | 7347 |
rs370974436 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595553 | AGTGAGCCGAGATCG[A/T]GCCATGGTACTCCAG | 7347 |
rs371007368 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567552 | AGTTTGATTTACAAA[-/T]TTTTTTTTTTTTTGA | 7347 |
rs371047402 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585288 | GAAGAACAAAGATAA[A/C]TGGAAAATGTTCAAG | 7347 |
rs371066641 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600015 | CAAAACAGTATTATT[A/G]CTGATATGGAGAAAG | 7347 |
rs371068168 | snp | C/G/T | 3.30149e-05 | 0.00406283 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569443 | TTTTCCAATGAATAC[C/G/T]TTTATTCTTATTACA | 7347 |
rs371068485 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602975 | CTGCCATTTTTTGTT[C/T]TTATTTTATTATGTT | 7347 |
rs371178269 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559120 | TCTCTGCTCACTGCA[A/C]GCTCCGCCTCCCGGG | 7347 |
rs371408920 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75594947 | GAAAGTAGATCTTCA[C/T]TTTATTGCATTAGTT | 7347 |
rs371424841 | snp | A/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605848 | CAAAAACTGTATTAT[A/T]TGCAACTAAATTTTC | 7347 |
rs371555657 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577922 | AGAGATCACCTTATG[A/G]TTTATTGTTTAACTT | 7347 |
rs371661514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554423 | GCTCTCCATGAATGT[C/T]GGCTATTTTTAATAT | 7347 |
rs371688372 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555497 | GGAAGAATGAATAGA[A/T]CTTATAAAGCTGCTT | 7347 |
rs371706010 | snp | A/G | 3.41134e-05 | 0.00412983 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569537 | TTCTAAATTTTTCTT[A/G]CTATAAATTTAACCA | 7347 |
rs371815142 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604483 | GATAATTTTTAAAAA[A/G]CTGACAATAATTTTG | 7347 |
rs371830387 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587348 | AATTTAATATCTGTG[C/G]TTAGATTAGATCCTG | 7347 |
rs371906549 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596270 | ACCCTGAGCGTTGTC[C/T]ACAATACTAGAGTGA | 7347 |
rs371998140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575591 | TCATCCCCCTTCTAT[A/G]GATGAGGCAATTGAG | 7347 |
rs372048057 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575581 | ACCATTGTCCTCATC[C/T]CCCTTCTATAGATGA | 7347 |
rs372117053 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583401 | TTTTTATTAGAAAAC[A/G]TGATGCTCAAAAAGA | 7347 |
rs372121001 | snp | C/T | 6.66656e-05 | 0.00577307 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549875 | GAGGTGGGCGCGCTT[C/T]GGGGCAGCCCTGGGC | 7347 |
rs372214644 | snp | C/T | 6.58892e-05 | 0.00573936 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550009 | GAGGTGTCTGTCGCT[C/T]GGGACCTCGGAGTCT | 7347 |
rs372227026 | snp | C/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598042 | CATTGGGATTTAGAG[C/G]TGGATTTGGAACTGA | 7347 |
rs372248094 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561747 | TCTACATATTTTAGT[-/C]TTTTTTTCTAGAATG | 7347 |
rs372411768 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584072 | AACAAAGCCTAAAGA[C/T]CTTGAGACAGAAAAC | 7347 |
rs372557241 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565226 | TTATTTTGCTTTGTC[A/G]TCAGGAACATTAACA | 7347 |
rs372669648 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586450 | TGTCAACACTCAGAA[A/T]CAATAAAAAGATACA | 7347 |
rs372831542 | snp | A/G | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606266 | TATGTTATTGTGAGA[A/G]GAGATAAGTAACAAA | 7347 |
rs372865600 | snp | A/T | 0.000829728 | 0.0203513 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605707 | TACACTGAAAAATCA[A/T]ACTTTTTTTTTTCCT | 7347 |
rs372889994 | snp | A/G | 3.3942e-05 | 0.00411945 | missense | UCHL3 | GRCh38.p7 | 13:75560828 | CCTGAACTCCTTAGC[A/G]TGGTACCAAGACCAG | 7347 |
rs372909219 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550720 | CCTTATTTTACCCTG[-/T]TTTTTTTTTTTTTTT | 7347 |
rs372969830 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592457 | ATATATATATATATA[C/T]ATATATATATGAAGG | 7347 |
rs372972981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584991 | CAACAGCTGTGGGAC[A/C]ATTTCAAGTGATGTA | 7347 |
rs372973190 | snp | C/G | 0.00031326 | 0.0125113 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594911 | TTTTTCCCTCCTATT[C/G]CAGGCACCAAGTATA | 7347 |
rs373012459 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589055 | TTATTTCTCTCCTTA[A/G]CAGTATGTGTCCCAT | 7347 |
rs373016721 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571272 | CATACTTCTCTTGCC[C/T]CATTTTTGGAGTTTC | 7347 |
rs373035552 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597129 | TGGCAGTAACTCTGA[G/T]GCAGATCTAATAAAT | 7347 |
rs373053231 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579706 | CCAGATCTGACTAGA[G/T]GAAACTCGTCTAAGA | 7347 |
rs373126097 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549641 | AAATATGACACTTGA[C/T]CTACGGCCCTGCACG | 7347 |
rs373283842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588507 | TACACTTTTGTTCCC[A/G]TATAGAATCAAGTAT | 7347 |
rs373374065 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572091 | CTTGTCTTTCTAACT[G/T]TAATTATTTCTTTTT | 7347 |
rs373384610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590521 | TCTTTGCCATCTATT[A/G]CTTTATTATTATTAT | 7347 |
rs373384963 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552181 | CTTTTAGTGGGAGAA[A/T]GGGCAAGTATGTAAG | 7347 |
rs373398852 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599698 | TGACTGCTCCATTAA[C/G]CAGCCATTTCCCCAT | 7347 |
rs373432605 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562128 | AAATGGAGCCAAATC[A/C]CACAGGATTTAAGAC | 7347 |
rs373536524 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576085 | TTGACAGCTAATTTT[G/T]TAGCAGTTCTGTTAA | 7347 |
rs373612651 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573318 | GGGCTTAAGAGTGTT[C/T]GGTGTATTATTATCT | 7347 |
rs373620676 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577941 | ATTGTTTAACTTTTT[A/C]AGTTTGTTGTACTGC | 7347 |
rs373627785 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558490 | GTGTTTTATAACTTT[A/G]TAACAGGATGACTTT | 7347 |
rs373659811 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576674 | TTTTATTTCTTTAAA[A/G]TGGGTTCATGATTGA | 7347 |
rs373713669 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555001 | CATGCGGTATTTGGT[C/T]TTCTGTTCTTGCATT | 7347 |
rs373757216 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600445 | GTTAATGCAGACGGT[A/G]ACTTTCAGTTGAAGC | 7347 |
rs373838223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550237 | CTTGGGGACTCCGGG[A/T]CTGAGGTTTGGAGGG | 7347 |
rs374003771 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596633 | CTTTCAGAATGAGAG[A/G]CTTACAGAGCAAACA | 7347 |
rs374041786 | in-del | -/C | 0.0229445 | 0.104622 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577963 | TTGTACTGCCCAGAA[-/C]CCCCCCATGTAAATT | 7347 |
rs374305257 | snp | C/T | 6.59087e-05 | 0.00574021 | stop-gained | UCHL3 | GRCh38.p7 | 13:75567286 | ATGAGCCCTGAAGAA[C/T]GAGCCAGATACCTGG | 7347 |
rs374605781 | snp | C/G | 6.83048e-05 | 0.00584361 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569538 | TCTAAATTTTTCTTG[C/G]TATAAATTTAACCAT | 7347 |
rs374864092 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547004 | TTTAAAAACACCTTA[-/T]TGTAATATATATTGT | 7347 |
rs375006984 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556390 | AGTTAATACTAGTTT[A/G]CTGGCAGTAATATCA | 7347 |
rs375018323 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603000 | TATGTTATTATTTTA[-/T]TTTTTTAGAGACAGA | 7347 |
rs375078899 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564604 | GTACCAATCTGCATT[C/G]CCACCAACAGTGCAC | 7347 |
rs375314560 | snp | C/T | 1.64885e-05 | 0.00287123 | missense | UCHL3 | GRCh38.p7 | 13:75594918 | CTCCTATTCCAGGCA[C/T]CAAGTATAGATGAGA | 7347 |
rs375530393 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551963 | AGTCATTAGCATTTA[G/T]TATAAGTACAATAAG | 7347 |
rs375549680 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573448 | AAATTGTTACCAGGT[G/T]CCTTTAACAACAGAA | 7347 |
rs375625755 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563155 | TATGTATGTATGTAT[A/G]TATGTATGTATATAT | 7347 |
rs375660336 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576926 | TGTAATGGTGGGTTC[C/T]TTACTTGTGGATTCA | 7347 |
rs375665851 | in-del | -/TTTATGTATGTA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563126 | GGTACCTCATTATCC[-/TTTATGTATGTA]TGTATGTATGTATGT | 7347 |
rs375686316 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587556 | TATGTAACTTATCTT[C/T]AAATGATTCAGGAAA | 7347 |
rs375744803 | snp | A/T | 0.00131314 | 0.0255899 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604882 | TGTCATCTTTAAAAC[A/T]TCTCTAAAGGTCACT | 7347 |
rs375929710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593542 | TGCCTCAAAACCTAG[C/T]GGAGGAGCCTCTGGC | 7347 |
rs375988465 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587017 | TTTACCTTAAGGTAG[A/C]AAAAAAAAAAAAAAA | 7347 |
rs376093532 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591479 | ATGAGCACAATTGAT[C/T]CAATTCTAATGTGAA | 7347 |
rs376235329 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566426 | ATGTTAATACATATT[A/G]CCATATGCCCTGTAA | 7347 |
rs376331835 | snp | C/T | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547186 | ATTTTAAACATTGAA[C/T]TCACTGACAAAAATC | 7347 |
rs376335972 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586312 | TATCTCACCAAGAAG[A/G]CATAGCATACACGTA | 7347 |
rs376340085 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566986 | TGATGATGGGAATGT[A/G]TATACTGTTAGAAGA | 7347 |
rs376497370 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605770 | TATGGAGCGCGACCC[C/T]GATGAACTAAGATTT | 7347 |
rs376557274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575524 | TTGCTACAGAAGTTT[C/G]ATATGTGTCATTTAA | 7347 |
rs376604086 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600435 | TGATTGTCTTGTTAA[C/T]GCAGACGGTGACTTT | 7347 |
rs376611194 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594116 | ATCATAGGAAGTGCC[A/G]GTTAATCAATGTATC | 7347 |
rs376613229 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585716 | ATAGCACATATAAAA[A/G]TAAAATAAGACAATA | 7347 |
rs376626341 | snp | A/G | 1.66735e-05 | 0.00288729 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75566835 | TATTGCAAACAATAA[A/G]GACAAGATGCACTTT | 7347 |
rs376726800 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557028 | TCAGACCAGCTTGGG[C/G]AACATAGTGAGACGT | 7347 |
rs376728987 | snp | A/T | 5.06402e-05 | 0.00503165 | missense | UCHL3 | GRCh38.p7 | 13:75566727 | AGAAGAGGAAGAAAA[A/T]ATAAAATCTCAGGGA | 7347 |
rs376817070 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598220 | ACATCCTCCCACAGA[C/T]TACCCAGATTCAATT | 7347 |
rs376883594 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595202 | AATTCAAAAATGTTT[G/T]CATACCATCTTCGCA | 7347 |
rs376987036 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601496 | GCAAGCCCCTCCATC[A/G]GCAAAAAGATGGCAA | 7347 |
rs377034466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550407 | CACCCAGTCCTTGTA[A/G]TTTCATCCACCGCCT | 7347 |
rs377123195 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577522 | CCTGAAACCAATAGT[A/C]CGTGGATATCGAGGG | 7347 |
rs377167038 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589322 | AAAAGCACCTGGCAT[-/A]AAAAAAGATGCGTAT | 7347 |
rs377282246 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570535 | GCCACCTCGCCCAGC[C/T]GAAACCACACTTTTT | 7347 |
rs377292343 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579108 | CAAAAATGATTTACG[C/G]ACAAATTGAGGTGCT | 7347 |
rs377298298 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586451 | GTCAACACTCAGAAT[A/C]AATAAAAAGATACAG | 7347 |
rs377416621 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75567300 | ACGAGCCAGATACCT[A/G]GAGAACTATGATGTC | 7347 |
rs377433323 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595842 | ATGGCATGTTGGAGG[A/G]GATCACATAATTTAC | 7347 |
rs377460620 | snp | A/C | 8.73004e-05 | 0.00660625 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569556 | TAAATTTAACCATAT[A/C]AATTTCTTGCTGTAA | 7347 |
rs377547686 | in-del | -/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599152 | TTTTTTTTTTTTTTT[-/T]GTAAATTGGGGTCTA | 7347 |
rs377553995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572468 | ACAAAATGGTGTGTC[A/G]TGGAACCAATGGCGC | 7347 |
rs377629314 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573646 | GAGAGAGAGATCAAT[G/T]GATCTGATGTCTCTT | 7347 |
rs377631097 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591152 | AAAAGTCAATGGCAA[A/G]CATTCTTTCCTTCCC | 7347 |
rs377639576 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594740 | ATAACTGAGCACATT[A/G]TCACAAACACAGGCA | 7347 |
rs377746297 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590267 | CCCCCAATAAGATTG[C/T]AAGCATATCTCTATG | 7347 |
rs386379799 | in-del | -/ATA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555624 | TTTTTATTATAATAA[-/ATA]TATATAAGTAGAAGA | 7347 |
rs386772407 | in-del | CAGCCCAGA/GCTC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577891 | TATTAATTGAGGAGC[CAGCCCAGA/GCTC]TATGGGTAGAGATCA | 7347 |
rs386772408 | in-del | ATC/GA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581155 | GTAATTATTTTAACT[ATC/GA]TACCCACTAATGATC | 7347 |
rs397768992 | in-del | -/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590193 | TTTTTTTTTTTTTTT[-/T]CTTAACTTCGGTCTT | 7347 |
rs398023474 | in-del | -/A | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573284 | AAAAAAAAAAAAAAA[-/A]GATTCATCTCTCATC | 7347 |
rs527296371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589647 | TTGATGTAATAATTT[G/T]AGTGGCTTTTACATA | 7347 |
rs527332329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557304 | TCCTCACATACAAGG[C/G]TCTCAAAACATATTT | 7347 |
rs527380002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575239 | ACCTACTTTTCTCCA[C/T]CCCACCGTGATTGTC | 7347 |
rs527436111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551562 | TAAGAAATCCTCTAC[A/C]AAATATTAGCAAATA | 7347 |
rs527438338 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589047 | TATCAGAATTATTTC[C/T]CTCCTTAACAGTATG | 7347 |
rs527459607 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603297 | TAGCTCTTTAGTCTC[A/G]TGAATGACACACACA | 7347 |
rs527504353 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576291 | CTGGAGTGTAGTGGC[A/G]CAATCTCTGCTCACT | 7347 |
rs527531906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596734 | CTTAAAAAAAAACTC[A/G]GTTTTACTAGTTAGA | 7347 |
rs527627435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596271 | CCCTGAGCGTTGTCT[A/G]CAATACTAGAGTGAT | 7347 |
rs527667031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597925 | CTTTTGTTATCACCC[G/T]CCCTTTTCCTTGGGG | 7347 |
rs527668628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603001 | ATGTTATTATTTTAT[C/T]TTTTTAGAGACAGAA | 7347 |
rs527707976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586129 | TTTACAAGAAAGTCA[C/T]TTTAAAAAACGTAAG | 7347 |
rs527739660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591279 | TTCCATTTCTGCTGA[A/G]TATCAACAAACTCAC | 7347 |
rs527822751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590536 | ACTTTATTATTATTA[A/T]TTTTTTATGTTTCTG | 7347 |
rs527825972 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573146 | GCATGTGCCTGTAAT[-/C]CCAGCTATTTGGGAG | 7347 |
rs527827383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598668 | CAGAAATAATGCTGC[A/G]TTCTTCTCAGTGCAT | 7347 |
rs527855484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560292 | CTTAAAAACCAAGTG[C/T]TGGAAATGAGTTTAA | 7347 |
rs527860591 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568439 | CAGTACTCTTACTAA[A/T]GAGAGGTAGATAAAC | 7347 |
rs527890812 | snp | A/G | 1.64955e-05 | 0.00287184 | missense | UCHL3 | GRCh38.p7 | 13:75567259 | AAAAAATTCCTGGAG[A/G]AATCTGTGTCAATGA | 7347 |
rs527900086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575792 | AGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGTGCA | 7347 |
rs527970476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561126 | TTTTTGTAGAGACAG[C/G]GCCTCACCGTGTTGC | 7347 |
rs528032236 | snp | C/G | 5.83345e-05 | 0.00540036 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549814 | TGGAGGGCCGGGCAC[C/G]GCGGCCATGGAGGGT | 7347 |
rs528189684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550213 | TCCCATTCTGCAGTC[A/C]CCACGTATCTTGGGG | 7347 |
rs528229899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594080 | TAACTCATATTAATA[C/T]TAGCTGTATAGTTAC | 7347 |
rs528235995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572309 | CTTTATATGACTACT[C/G]CAACTATTTGCATTT | 7347 |
rs528487961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573939 | AGTCACTTTTCAGGC[C/T]GGGCGCGGTGGCTCA | 7347 |
rs528518792 | in-del | -/TTA | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590524 | TTGCCATCTATTACT[-/TTA]TTATTATTATTTTTT | 7347 |
rs528562129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565955 | TTGATGCTTATTATT[A/G]TACCCTATTGCTTTT | 7347 |
rs528581808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558342 | CTTGTTAGCTTTGGC[A/T]GACATAGAGTAGATT | 7347 |
rs528696172 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573873 | ACTTCCGGGTATACC[A/G]CTGCTCTTTGCAGAG | 7347 |
rs528760545 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575813 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 7347 |
rs528781387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573320 | GCTTAAGAGTGTTCG[G/T]TGTATTATTATCTCC | 7347 |
rs528786674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588032 | AAGTAATAATTTTTT[C/T]TTTTCTCTGACCCAG | 7347 |
rs528874026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602277 | CATCTCGTGATGTTT[G/T]TCATGTCGCTTGTCT | 7347 |
rs528897462 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564472 | CAGATATCTTTACAA[C/G]GTAGAGATTCATCTC | 7347 |
rs528905567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550251 | GTCTGAGGTTTGGAG[A/G]GACTTTTACCCTGTA | 7347 |
rs528916758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594745 | TGAGCACATTGTCAC[A/G]AACACAGGCATGGTC | 7347 |
rs528937356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588188 | CTGTTCTTTTCTCAC[A/T]CTGAATTCTTTGCCA | 7347 |
rs529015937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587511 | AGTCCTAGGAAATAC[C/T]GAAGAATTTAGGATT | 7347 |
rs529041088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595526 | CGCTTGAACACAGGA[A/G]GTGGAGGTTTCAGTG | 7347 |
rs529048894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564485 | AAGGTAGAGATTCAT[C/G]TCCTTTACAAGGTGA | 7347 |
rs529109335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573125 | AAAAATCAGCTGGGC[A/G]TGGTGGCATGTGCCT | 7347 |
rs529120579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601397 | GTGGCAAACTTCATT[A/G]TTGTCTTATTTTAGG | 7347 |
rs529148934 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583039 | GATATTTGTATAGTG[C/T]GTTCATTTAGCATGA | 7347 |
rs529161217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601746 | ATCTCTCAGGCATGC[C/T]TGTACATTTTTTAGA | 7347 |
rs529221600 | snp | A/G | 0.000330593 | 0.0128525 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566890 | TTTTTTCCCCCTTAA[A/G]ATACAAGTTAATTGC | 7347 |
rs529307517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596347 | AGTATATAATGGACC[G/T]CCAGGACAGTTTTGA | 7347 |
rs529352795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551771 | TACGTCCTGTGATTC[A/G]GCTGCTAGTGGACCT | 7347 |
rs529370415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559823 | CTATTCCTTTTTTCT[A/G]TCATCTAAAACTTAT | 7347 |
rs529539242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565501 | CTTGTAGGTTTTCTA[C/T]AGACATCGTTTGTTT | 7347 |
rs529575122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573947 | TTCAGGCTGGGCGCG[A/G]TGGCTCACGCCTGTA | 7347 |
rs529741170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562938 | CTTTTAGATGTCTTA[C/G]AGTTTTGTAGATCCC | 7347 |
rs529765541 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559407 | TCTTTGCTGAACACA[-/T]TCTTCTAAGAAAGTT | 7347 |
rs529801260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555353 | TGAAATTATCTTGTT[G/T]ATGTGTATACTTGTT | 7347 |
rs529915423 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557868 | AACTGCTAACATTTT[A/G]GAAAATTTCCTTCCT | 7347 |
rs529936061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577143 | AGCTACTCTGTAGTT[C/G]GGAGGCTGAGATAGG | 7347 |
rs529941252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569767 | TGCAGATTGTGTGCT[C/G]TTTGTGCGGCTTGGT | 7347 |
rs529971053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584643 | CAGAGCTAGACTCAT[A/G]TATGATCTAGATGTC | 7347 |
rs529981177 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561135 | AGACAGGGCCTCACC[A/G]TGTTGCCTGGTCTGG | 7347 |
rs530057650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586611 | AGTTACCAGGATAGA[C/T]CATATTCTGGATTAA | 7347 |
rs530136990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578465 | TAACCTGTTTGAGCA[C/T]CTACTGTACTAGGCA | 7347 |
rs530176242 | in-del | -/AT | 0.00676609 | 0.0577691 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563604 | TATATCTATCATCAC[-/AT]AGTTACTTTTTTTGT | 7347 |
rs530251689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579417 | ATTTTATTTTATTTT[A/T]TTTTTAAAACCAAAA | 7347 |
rs530280387 | snp | C/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550227 | CACCACGTATCTTGG[C/G]GACTCCGGGTCTGAG | 7347 |
rs530282989 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587123 | ACTGTAGTAGAGGTC[C/T]TAGCCAATATAGTAG | 7347 |
rs530321484 | in-del | -/T | 0.00256952 | 0.0357514 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566874 | TTTTTCATTACTGCA[-/T]TTTTTTCCCCCTTAA | 7347 |
rs530332085 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591053 | TACATTTATAAGAAA[C/T]TTGACATTTCTATAA | 7347 |
rs530341847 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552786 | GAATTACAACATTTA[C/T]AGAGTGTGATATAGG | 7347 |
rs530374048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585973 | GAAAAAATAAAGAAC[G/T]GACAATGTAGATTTA | 7347 |
rs530586808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570802 | CTGTAGCACTAGCTA[C/T]TAGGGAGGCTGAGGT | 7347 |
rs530644948 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549419 | ACGCCTCCTAGCGCA[A/G]TCGGTTGACACTGCA | 7347 |
rs530737851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577309 | TACTGAATATATACA[G/T]ACTTTTTTCTTGTCA | 7347 |
rs530778112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573229 | ATATCCCACCACTGC[A/G]CTTCAGGCTGGGCAA | 7347 |
rs530814219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580371 | GAATTAATTTATAAT[G/T]TTGATTTTAAACTCA | 7347 |
rs531007462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564584 | TACTGTTTTTCATAA[C/T]GGCTGTACCAATCTG | 7347 |
rs531013243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573863 | AACCCAGTACACTTC[C/T]GGGTATACCGCTGCT | 7347 |
rs531040642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549722 | GCTCCTCCTCCGGGC[C/G]GTGTGTTGGGAGGGC | 7347 |
rs531106845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587270 | CTTGATGTTTAAAAT[A/G]TAAAAGATAAAGACT | 7347 |
rs531142459 | in-del | -/AAAAC | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602113 | GACTCTGTCTCAAAA[-/AAAAC]AAAAACAAAAACAAA | 7347 |
rs531227672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579589 | CTCCTTTCCTCCCCC[C/T]TTCTTTCTTCTTTTC | 7347 |
rs531236058 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599012 | ATGCTCAAATTACTG[C/T]AGACTTGGCCTTTGA | 7347 |
rs531343093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583076 | AAAAATAAGTCTGAC[C/T]AGAGTAAAAATTTAG | 7347 |
rs531414835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568503 | CACAATTTTTTAAAC[A/G]AGAATTTGATCATAC | 7347 |
rs531465767 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573718 | CATTCTTATAACCTT[A/G]GTTAACATTAACTAC | 7347 |
rs531533025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597746 | TATGGAGAGATGACT[A/G]TAACTTTATTTTTAA | 7347 |
rs531539900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589682 | TTTCCATGAGTCTGT[G/T]CTATGCAAATGAGGA | 7347 |
rs531557809 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586140 | GTCATTTTAAAAAAC[A/G]TAAGAAGATAACAAT | 7347 |
rs531559831 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548309 | CAATCCATTAGATAA[C/T]GATGAAGAGGAGTTA | 7347 |
rs531578613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552689 | AAATTATTTAAACAT[C/T]TTAAACTCTACTTTA | 7347 |
rs531584727 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601615 | CTAATGTATACCTAA[C/T]AGACTACAGAGTAAT | 7347 |
rs531628668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590335 | ACATCCATCTTTCCA[C/T]TCCATATCCTGCCAA | 7347 |
rs531821035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561295 | CAATCTTTAAGAACA[A/G]ATGATCCCCTTCTTG | 7347 |
rs531828837 | in-del | -/ATTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578248 | AGTAAACCACAATTT[-/ATTT]TTCATTTCCTTAACT | 7347 |
rs531971780 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586086 | AAAGATCAGTTTAGT[-/A]AAAAAAGCAAGACAC | 7347 |
rs532073619 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605988 | GTTAAAGGTGCAATG[C/T]TTTCCTCCTCTTTTC | 7347 |
rs532076425 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605873 | ATTTTCTCTGCCATA[C/G]ACTAACTCAAAAATT | 7347 |
rs532086004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570426 | TATTTTTAGTAGAGA[C/T]GGGGTTTCCCCGTGT | 7347 |
rs532098102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569559 | ATTTAACCATATAAA[C/T]TTCTTGCTGTAAATT | 7347 |
rs532136283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576358 | CCTCAGCCTCTCAAG[C/T]AGCTGGGACTACAGG | 7347 |
rs532187170 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556557 | AGTGAATTTTATCTA[-/T]TTTTTTTAATTTATA | 7347 |
rs532271916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584026 | TGCTGCTGTGGGAAA[A/G]GCGTGAAGCCTGGAT | 7347 |
rs532294743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575940 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 7347 |
rs532564123 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584907 | CTGGAAATTACCCAA[A/T]CTTACTCACAAAGGG | 7347 |
rs532617213 | snp | C/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547989 | GTCCCTGCTGGGATG[C/G]AAACTGTCTTGCTGT | 7347 |
rs532646685 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602026 | AGGCAGGAGAATGGC[G/T]TGAACCCGGGAGGCA | 7347 |
rs532648975 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574062 | ATCTACTAAAAATAC[A/G]AAAAAACTAGCCAGG | 7347 |
rs532655279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600350 | TCTCTTGGGAAGAAG[A/G]TGCCATCTAGGACTT | 7347 |
rs532690720 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585840 | TAACTAAAGATATAT[A/C]TTGTAAATCCTCAGG | 7347 |
rs532792802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554549 | TCCATTTCAGCTGCC[A/G]CAGTGCAAGCCACCA | 7347 |
rs532804948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592087 | GCCTGGTGGTATGTA[C/T]TAAGTGCTATACAAT | 7347 |
rs532859386 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548348 | AAATACCTCTGAAGT[C/T]AAAGAACAGTGGCCA | 7347 |
rs532880259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599610 | CTTTGATATTACTAC[C/T]GTAATTGTTTTGGGA | 7347 |
rs532972117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551461 | AGACACTTCCTAACT[A/C]ATTTTATGCTAGCAT | 7347 |
rs532980471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588239 | CCATCCCAACTTTAT[A/G]TATTCTTTCAGTATA | 7347 |
rs533085524 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576508 | TACAGGCGCGTGCCA[C/T]CACACCCAGCTAATT | 7347 |
rs533090917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550876 | TTTTCAAAGCTTGTA[A/G]CAAATTCCCTGGACA | 7347 |
rs533096080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588830 | TTCTCACTATGATTG[C/T]AGTGATTGTAATTTT | 7347 |
rs533111498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560985 | GCCTAGGCTGGAGTG[C/T]AGAGGTGTAATCATG | 7347 |
rs533125122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602409 | CACTATTTTCTTCCC[C/T]GTCCAGCCTGGAAGT | 7347 |
rs533142638 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580579 | CTCCTCAAAATTGTT[C/T]GAGGTGCTCACCAGC | 7347 |
rs533158920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604420 | GAGATCTTCCTATTT[A/T]AAGTGAAAAAAGAAA | 7347 |
rs533192329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559282 | CCTGACCTCGTGATC[C/T]ACCCGCCTCGGCCTC | 7347 |
rs533197168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560152 | GCTTATATTACTCTT[C/T]GCTCATTGATACAAT | 7347 |
rs533364061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574526 | GTTTGTATACTGACT[C/T]CACTGCTTATTAGCT | 7347 |
rs533425221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597838 | ACAGAGAATGGTGGT[A/G]GTCTTTAATGTATTA | 7347 |
rs533426525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567123 | TCTAACCTACCAATG[A/G]AAGAATTTAACCTGA | 7347 |
rs533484581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553633 | GTGTTTTCTTGCCCT[A/G]GTAATGTTTTCTGTT | 7347 |
rs533515883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604949 | TCCTTGTTCTCTCTA[A/G]AAAATCCAAAAAGAA | 7347 |
rs533535938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575150 | TAAATGAAAAATCTG[G/T]AAGTTGAGTCACCAA | 7347 |
rs533879692 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555450 | ACGGTGCCAGGCTCA[C/T]GGGGCCATCAACAAA | 7347 |
rs533909463 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574634 | TAATTATATAAACTG[C/T]TTAGAATAGTACCTG | 7347 |
rs533954068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587823 | GCAACCTTAAGGGAT[A/G]AGGTAATGTCTTTGC | 7347 |
rs533984745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583261 | TGCTATCCTATTTTG[A/G]ATGTTGTAAAACATT | 7347 |
rs533987791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575500 | TAGAATAAAATAGTG[A/T]TATTAGAGTTGCTAC | 7347 |
rs533995767 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566338 | CATAATATATTTTAA[A/C]CAAATCTCCATTGAT | 7347 |
rs534033580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581074 | TTTTTTCCTATTAAC[C/T]GGAAATCTTACCCAT | 7347 |
rs534101229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552095 | TATTTAGTATATGAT[C/T]GTACATTATATCTGG | 7347 |
rs534128204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580686 | ATTTTCTGAATTCAT[A/G]TTATGGGGCAGGCTA | 7347 |
rs534208330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553123 | AAATAATCACAATAA[A/G]TAAATCATATAAATT | 7347 |
rs534223689 | snp | A/G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565930 | GCAGTCAGCTATAGA[A/G/T]CCCACATTTTTGATG | 7347 |
rs534229368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596527 | GAGTGCTGGGACTTA[A/G]CAGACACATTCTGTT | 7347 |
rs534300882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593161 | AGTATTTCATATCCT[A/G]TTGGAAAATTGTCTT | 7347 |
rs534361554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549473 | ACGCGGTCCCAGACC[A/G]GCGCAAGGCGCATGC | 7347 |
rs534368836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586780 | TCTAAATAATTCATG[C/G]ATCAAAGAGGAATCA | 7347 |
rs534376014 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578836 | TCATCATAAATATAT[A/G]TACATAATTAAAGAT | 7347 |
rs534476508 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600680 | GCACCTTGTAATCCA[A/T]GAAGTCCGATATAGA | 7347 |
rs534482476 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555477 | CAAATATGTAGTTGT[C/T]AGATGGAAGAATGAA | 7347 |
rs534519688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562537 | ACAGTAAATAATTGA[A/G]AAAAAAATCAGTTGC | 7347 |
rs534537393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602754 | TAGCTTAAAGGAGGC[A/C]TTAAAAATACACTGA | 7347 |
rs534545986 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574359 | AGTTTTTTCTTCCTT[A/G]TGTATATTTGTTTAT | 7347 |
rs534583551 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555842 | AAACAATTCTGCCAC[A/C]TCAGCCTCCTGAGTA | 7347 |
rs534739902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595806 | TTTTTTTTTTAAGTT[C/T]ACCTTTCAGTGGACT | 7347 |
rs534799754 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568070 | AACTAGGCTATATAT[A/C]TAATATAGGTTATAT | 7347 |
rs534882542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592394 | GTGTTTGGATGTAAA[A/G]TGGAATTTTAATTTT | 7347 |
rs534901656 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548750 | GCCCTGGATAAATAA[C/T]GTGAAGAAGAAAAAA | 7347 |
rs534987609 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550059 | CTTCCCTGCTGGACT[C/G]CACCTCCACGCTTCC | 7347 |
rs534989873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557571 | GGTTATGAAACCTTT[C/T]ATCCTGCTTGATGTA | 7347 |
rs535042855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572654 | AACTGTCCTTGGTAG[C/T]GTAAGAAATAAAAAA | 7347 |
rs535105760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550375 | CACTTCCTGACTCCA[A/G]GCTTTGTAAACTCGC | 7347 |
rs535204082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579744 | CAGCAATAAAAATAG[A/T]ACTGATGTTGTGTTT | 7347 |
rs535244132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571819 | TTTCCCATCTCCCAC[A/C]GTTTAGAAACACTAC | 7347 |
rs535245498 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549529 | TCGGCTCGGAAGAGT[A/C]CAAGCGTGAGGGGAG | 7347 |
rs535349329 | snp | A/G | 3.59305e-05 | 0.00423839 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549834 | CCATGGAGGGTCAAC[A/G]CTGGCTGCCGCTGGA | 7347 |
rs535439715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602692 | GTAGTAAATATTTTA[G/T]GTTTTGTGGGCTACA | 7347 |
rs535597432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595910 | GGTATACAATACTTA[C/T]TATGACTTCTTCTTA | 7347 |
rs535615437 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574854 | GAGTTTTTTTGGGTC[A/C]TATGTGTAGGAGTCT | 7347 |
rs535629568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600736 | TCATTTCTGCTAACA[A/C]AGCATCCATTCTGCA | 7347 |
rs535672492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573449 | AATTGTTACCAGGTG[C/G]CTTTAACAACAGAAA | 7347 |
rs535698953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586281 | GAAGAAGGACATTAC[A/G]TAAGGATAAAGAGGT | 7347 |
rs535717985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602002 | TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG | 7347 |
rs535752607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562724 | TATTATCCTTATCAA[C/T]AGGATTTAATTTAGT | 7347 |
rs535761778 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592271 | GAAGTCAATGGTACT[A/T]TTTATACTAAAAGAG | 7347 |
rs535794522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601350 | AGCATCACATGCTAC[A/C]GAGAAATCTTTCATA | 7347 |
rs535805827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564831 | CTCTGGAGTAGCTGG[A/G]ATTACAGGCATGTGC | 7347 |
rs535835228 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606121 | GCATAACATGAATAT[A/G]TATTATCTATGTTAA | 7347 |
rs535849899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558429 | TTCTAACTGTGACTT[C/T]TAGTTTGCAGCACAG | 7347 |
rs535946950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599112 | TAGCTGGGACTGTAG[A/G]CCTGTGCCACCATGC | 7347 |
rs535993667 | snp | C/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551336 | CTTGGGAGGCTGAGG[C/G]AGGAGAATCGCTTGA | 7347 |
rs536013304 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583541 | CTATAGTTTAGAACA[C/T]CTGGTAAAAGATAGT | 7347 |
rs536032372 | in-del | -/GAG | 0.0126979 | 0.078662 | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75595981 | ATAAACAACAAAAAA[-/GAG]AAGTTCTTTTCAGTA | 7347 |
rs536062912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575996 | GCTTCAGGTGATCTG[A/T]CTACCTCGGCCTCCC | 7347 |
rs536076524 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587069 | ATGCATAAAAGGTAG[A/G]AATAACAAAGGTAAA | 7347 |
rs536079713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567799 | GCAGTCCCTCCACCT[C/T]GGCCTCCCAAAGTGC | 7347 |
rs536113937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605315 | GAGTTCGAGACCAGC[C/G]TGACCAATATGGTGA | 7347 |
rs536228238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554592 | ACAACTATAGTAGGC[C/T]CCTAACTAGTTCTTC | 7347 |
rs536260320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554176 | CAAGCACTCCTCACA[C/G]CTCAGCCTTCCAAGT | 7347 |
rs536312472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591653 | TAGTAGTAAAGAACA[C/T]GGATTCTAGAAGCAC | 7347 |
rs536542731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561542 | AATACAGTTTTTTCA[A/G]TATATATATATATAA | 7347 |
rs536582156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568884 | GATTGTACTTTCACC[C/T]GTAATTTACTATTGT | 7347 |
rs536586577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584981 | ACAGTGCATCCAACA[G/T]CTGTGGGACAATTTC | 7347 |
rs536636440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599832 | TCTCTCACTTTAAGT[C/G]AAAAACTAGAAATGA | 7347 |
rs536636551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591785 | GTATAATTATATTAC[A/G]TACCTTATTGGGTTT | 7347 |
rs536689068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555420 | TGAGAGCAGGGATGC[A/G]TCTGAAGTATGAGAA | 7347 |
rs536745761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555507 | ATAGATCTTATAAAG[C/T]TGCTTTCCTGCTCCA | 7347 |
rs536787361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562668 | AAAATAAATTAGATT[A/T]GATCTCTTTCATTTA | 7347 |
rs536799071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592336 | ATAGTCATACTACAT[C/G]TATGAAGTGTCAATA | 7347 |
rs536834214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584453 | CCAATGGTATTCTCA[A/G]GGTAATCATAGCAAC | 7347 |
rs536852397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570009 | CCTTTCCTTCTCTTG[C/G]CTCTTTTTTCATTTT | 7347 |
rs536852600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561570 | TAAGGAATCTTCTTT[G/T]CTTATTTTAAGTTGG | 7347 |
rs536904003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577501 | TTTTGGTGTCTTCAG[A/G]GGGGTCCTGAAACCA | 7347 |
rs536989394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576744 | ATAAAGCTAAGCTTT[C/T]AATTGACTAATGTGT | 7347 |
rs537330453 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572443 | GGCGTTATTCCCATC[A/T]TAGTGGTTCACAAAA | 7347 |
rs537409135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564210 | GGCTGGAGTGCAGTG[A/G]TGCGATCTCGGCTCA | 7347 |
rs537443765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563294 | GATTCTTCTGCCTCA[A/G]TCTCTGGAGTAGCTG | 7347 |
rs537447530 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572534 | TCTGTGGCTCTTAGG[A/C]CTAGCATTGGCATCT | 7347 |
rs537522554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552200 | CAAGTATGTAAGAAA[C/T]GGTTATAACTAAAAA | 7347 |
rs537555164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603855 | AGGCATTGTAATTTA[A/G]GGATAAGTTTCTTTA | 7347 |
rs537665126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581194 | TGTTCAAGAAATTAC[A/G]TGGTTATAAGGATAT | 7347 |
rs537696978 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580443 | ATGTCCTTACACATA[C/T]GTGTACACACATTTA | 7347 |
rs537845581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566529 | TGGCTACTGCTATTC[A/C]TTTTTCAATCTTTTG | 7347 |
rs537921371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604518 | TTATTTTCAGGAAAC[A/G]AAAGCCAGCATTGTA | 7347 |
rs537945135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576501 | CTGGGACTACAGGCG[C/T]GTGCCACCACACCCA | 7347 |
rs538026340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554054 | AGTTCCTTAATTTCT[G/T]TCTTTCTTTTTTCCT | 7347 |
rs538064850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589130 | CAGTGATTAAGATCA[C/T]TGGACTCTAGAACTT | 7347 |
rs538172179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574086 | AGCCAGGTGTGGTGG[C/T]GGGTGCCTGTAGTCC | 7347 |
rs538173678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581947 | TATTCAGGAATTCAG[A/G]TAGAAATAGTAATAG | 7347 |
rs538255804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568572 | GAAACGTATTACATA[C/T]CAGTAAGTATATATT | 7347 |
rs538428309 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597316 | GTGTGCTATGATTGC[A/C]CCTGTGAACAGCCAC | 7347 |
rs538472574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553155 | TCATAAGAATTCTCT[A/G]ATTAGTAGATACCAT | 7347 |
rs538480711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574823 | CATTTACTTTTCAGC[C/T]TACTGAGTTTAAGGT | 7347 |
rs538499304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590759 | TGAAGATTTTCTCCT[C/T]GTGTATTGATGTAGG | 7347 |
rs538550789 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584760 | GAATTGGAAACTATT[-/A]ACATAAGAAAGAATC | 7347 |
rs538603989 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561412 | CTAGGTTAGTGCTTT[A/C]AGCTTTGGTAAATTT | 7347 |
rs538640779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560606 | CCTACTGAATGTCAG[C/T]TACATTTGTATTTTA | 7347 |
rs538745635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561875 | CATATATACATACGT[A/G]TATACGTATACATAT | 7347 |
rs538755974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570821 | GGAGGCTGAGGTGGG[A/G]GGATTACTTGAGCTC | 7347 |
rs538912007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567698 | GATTTCAGGTGCGTG[G/T]CACCACACCTGGCTA | 7347 |
rs538948703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575395 | ATGAGGAAACAATGA[A/G]GAAATTAAATTATTA | 7347 |
rs539004777 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597848 | GTGGTAGTCTTTAAT[A/G]TATTAATTCCCTACT | 7347 |
rs539006993 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568574 | AACGTATTACATACC[A/C]GTAAGTATATATTTG | 7347 |
rs539046856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576601 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 7347 |
rs539075896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580588 | ATTGTTCGAGGTGCT[C/T]ACCAGCTTTCAAGTA | 7347 |
rs539137991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564925 | GGTCTTGAACTCCTG[A/G]CCTCAGATGATCCAC | 7347 |
rs539159805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570046 | TCTTCATTTTTCCTT[C/T]CATCTTTTCTTTCTT | 7347 |
rs539213294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590845 | AAAAATACATTTTTC[A/T]TATAATCTTGCTAAT | 7347 |
rs539290459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584317 | GGAGAGAGACCTTCT[C/G]TGAGGCATAGCCTCT | 7347 |
rs539351324 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551832 | ACACATTAATATTTT[A/T]GGGGCACCTTTTTTA | 7347 |
rs539498124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582006 | TTGACAGTTGATGGG[C/T]GAGTGACCTTGCAAT | 7347 |
rs539509971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573993 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 7347 |
rs539538069 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570130 | AGGTATTTTAGTCAA[-/AAAG]AATTTAACTAAAGCT | 7347 |
rs539604718 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601851 | GTGGTAGCTCACGCC[A/T]GTAATCCCAGCACTT | 7347 |
rs539647352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565591 | AGCTTTGCAGGCCTT[C/T]AAGTGTCTGTTGCAA | 7347 |
rs539690573 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568254 | TAATCTACAAATTAT[C/T]TGGTTAGAACAATGC | 7347 |
rs539709904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75595996 | GAGAAGTTCTTTTCA[A/G]TAATTCTAGATACCG | 7347 |
rs539725266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551168 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 7347 |
rs539739536 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564624 | CAACAGTGCACTTGG[A/G]TTCCCTTTTCTCCAC | 7347 |
rs539792961 | snp | A/G | 1.6489e-05 | 0.00287128 | missense | UCHL3 | GRCh38.p7 | 13:75594934 | CAAGTATAGATGAGA[A/G]AGTAGATCTTCATTT | 7347 |
rs539794578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586922 | TAGAAAAAAACAAAC[A/C]AACAGAGGTTAGAGG | 7347 |
rs539859596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551837 | TTAATATTTTAGGGG[C/T]ACCTTTTTTAATACC | 7347 |
rs539862246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557317 | GGGTCTCAAAACATA[C/T]TTACAAATAATTTTA | 7347 |
rs539879625 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552155 | AATTGATTTTTTAAA[C/G]AAATAATGTGCTTTT | 7347 |
rs539921477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595454 | AATGCAAAATTAGCC[C/T]GGCGTGGTGGCACAT | 7347 |
rs539930124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589178 | TCCCGGTTCTGTTAC[C/G]TACTGGCAATGTGAC | 7347 |
rs539970211 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557923 | ATTTCAAACACAGGG[G/T]TTTTTTTTTTTAATT | 7347 |
rs540090747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603474 | TGTCTCTAAATTAAA[A/T]AGAAGAAAGAAAAAT | 7347 |
rs540207748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572994 | TCCCTGCCGGGCATG[C/G]GGGCTCACGCCTGTA | 7347 |
rs540214771 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574276 | CTGTTAAGTAGGTCC[C/T]TCTGTATTTTTTTTT | 7347 |
rs540269022 | in-del | -/G | 0.0133597 | 0.0806311 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599153 | TTTTTTTTTTTTTTT[-/G]TAAATTGGGGTCTAG | 7347 |
rs540301372 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600999 | TGGATGACTTTGAGG[G/T]GTTTAAGACTTCATT | 7347 |
rs540339938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602212 | TTCACGTCGTTGGCC[A/G]TTGTTGGGTATTTGA | 7347 |
rs540415664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566002 | GATAATGGTTAGTGT[A/C]AGTTACAGATTATAT | 7347 |
rs540601801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585319 | GCAGCCACATGAAAA[A/C]GACAGAGTAGATACT | 7347 |
rs540607886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577051 | GGCCAGGAGTTTGAG[A/G]CCAGCCTGGGCAACA | 7347 |
rs540672120 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596464 | GGAAGCAGATTTTCT[A/G]CTCTGAATTGTGAAT | 7347 |
rs540729507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571163 | GATGATGAGGATCAG[A/C]GTAAGTTTATTGTTA | 7347 |
rs540735949 | snp | C/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598424 | CATTACAGTTTTCCT[C/G]ATTATCACAATAATG | 7347 |
rs540774781 | snp | C/T | 0.101301 | 0.200969 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577895 | AATTGAGGAGCCAGC[C/T]CAGATATGGGTAGAG | 7347 |
rs540776266 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570133 | TATTTTAGTCAAAAA[G/T]AATTTAACTAAAGCT | 7347 |
rs540817802 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591186 | ATTTACCCTTCTAGT[A/G]TTATACTCAAACTGT | 7347 |
rs540836386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554900 | TTTCTGATCCTCTCC[C/T]CAGCCTTCACCTTCA | 7347 |
rs540893332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584583 | ATTTATCACAGTCTC[C/T]ATACTCCTAGAGAAG | 7347 |
rs540927048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588666 | GAAGGTACTAAGTAG[A/G]ATTAGAGAATTTTCA | 7347 |
rs541035844 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563369 | TTTAGTAGAGACAGG[A/G]TTTCACCATGTTGGT | 7347 |
rs541060452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593709 | TGTTGAATTTCTTCC[A/G]TTCATAATTTGAGGG | 7347 |
rs541069811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594412 | CAAAGACTGTTTACA[C/T]TGCACTGTTGAAACA | 7347 |
rs541095328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600978 | ATAAGTTGGTTCCAA[C/T]CCTCATGGATGACTT | 7347 |
rs541108489 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576611 | CACCCGCCTCAGCCT[C/T]CCAAAGTGTTGAGAT | 7347 |
rs541190698 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573093 | AACATGGTGAACCCC[A/G]TCTCTACTAAAAATA | 7347 |
rs541257983 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606284 | GATAAGTAACAAACA[C/G]ATCAAGATAAATACC | 7347 |
rs541302126 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573266 | CGAGACTCTGTCTCA[-/G]AAAAAAAAAAAAAAA | 7347 |
rs541443152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579003 | TGTATATGTATAGTT[G/T]CATGGCTTCATTTTA | 7347 |
rs541444652 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549604 | TGGCTTATTTTTTTC[C/T]CCTCGGCAGCATCTT | 7347 |
rs541499573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556947 | TACACTGGGTTGAGT[A/G]CAGTGGTTCACAGCT | 7347 |
rs541517630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594483 | TGACATCTTAAAATT[C/T]AACTCGAAAAGAGTT | 7347 |
rs541556194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572005 | CTTGTCTTGTCTTGT[C/T]TTGTCTTGTCTTGTC | 7347 |
rs541626205 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557216 | GCAAGACCCTGTCTG[-/A]AAAAAAAAAAGGAAG | 7347 |
rs541633363 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548843 | GCTTAAGATCCTTCA[G/T]TGGTTCCTTGCTGTT | 7347 |
rs541643241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592598 | TGTTTTTAGTGGAAT[A/G]ACTTTTAAGCAATTA | 7347 |
rs541727077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600390 | GAGAGGAGATGTCAA[C/T]ACCTGCCTTCAAAGC | 7347 |
rs541743987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556349 | TTTCTCATTTAACTA[A/G]TAGTTATTCTACTTC | 7347 |
rs541747256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563570 | ATAGTAAAATAGTTA[A/C]AATAGTGAAGCAGAT | 7347 |
rs541803780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585385 | GAGGTTATGCAAGCC[A/G]GAACACATAGAATGA | 7347 |
rs541869923 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578152 | TTTGACTTTTTTCTT[A/G]ACATATTACCATGAA | 7347 |
rs541939440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562939 | TTTTAGATGTCTTAC[A/G]GTTTTGTAGATCCCT | 7347 |
rs542018691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601096 | TGTGACTGAACTGCT[A/G]CAATCTCATGATAAA | 7347 |
rs542052148 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588569 | TTCTTATTATGAGCC[A/G]CTAAAATGTTCAAAC | 7347 |
rs542127195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593780 | TATATATAAATGTTT[C/T]AGAAACATTCTGTAT | 7347 |
rs542206711 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600826 | GTGAGACTATAGCTG[C/T]CACAGTGATTGCTTT | 7347 |
rs542263251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580712 | GGCTAACTAAGTGCT[C/G]TATCTACCCTAGTTT | 7347 |
rs542314712 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581431 | CTTGGCTCCCTGTAG[C/G]CTTGATCTCCTGGGC | 7347 |
rs542314923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583841 | CTAAAAATTTTAACA[A/G]ATTGCTTAAGGTCAA | 7347 |
rs542403056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590978 | ACTATTAAAGGCAAT[A/G]ACTGTGGTTTGGCAG | 7347 |
rs542407363 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549660 | CGGCCCTGCACGGAG[C/T]GGTTAAGAGGGTGAG | 7347 |
rs542408036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75604183 | CTTTGGGTTAGCATG[A/G]GTTTAAATAATTCTG | 7347 |
rs542409692 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553341 | CTGTGTGTACCATTT[C/T]GTAGTAACTTTTTTT | 7347 |
rs542485570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597653 | TATACCATTTAGGTA[A/G]AGTATGTCAAGGGGC | 7347 |
rs542491686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601972 | AAATTAGCTGGGTGT[A/G]GTGGTGGGTGCCTGT | 7347 |
rs542510579 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570379 | TCGCTGGAACTACAG[A/G]CGCCCGCCACCATGC | 7347 |
rs542518179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550124 | CTTGTTCGGCTTTAC[A/G]CGGGTCCGCCCCTTT | 7347 |
rs542522335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604703 | GGGGAAGAGGAAAAT[A/G]GAAGTTGAAAGCACA | 7347 |
rs542587408 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560695 | TATGTATAGTATACT[A/T]GTTTTCTTTTACCAA | 7347 |
rs542589006 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590164 | CGTCTCTTCTTCCAG[G/T]GACAAGGGCTGTCTT | 7347 |
rs542787847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554998 | GAACATGCGGTATTT[C/G]GTTTTCTGTTCTTGC | 7347 |
rs542836582 | in-del | -/AAAAC | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602125 | AAAAAAACAAAAACA[-/AAAAC]AAAACAAAAACAAAA | 7347 |
rs542895932 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599108 | TGAGTAGCTGGGACT[A/G]TAGGCCTGTGCCACC | 7347 |
rs543113353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600026 | TATTGCTGATATGGA[A/G]AAAGTTTGAGTGGTC | 7347 |
rs543151586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599524 | TGTGTTTCTGTGTCA[C/T]GCTTTGGTAATTCTC | 7347 |
rs543151918 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549415 | CGGCACGCCTCCTAG[C/T]GCAGTCGGTTGACAC | 7347 |
rs543154528 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594516 | TTTAAGCTGTTAGGT[A/G]TAAAAATATTTTAAC | 7347 |
rs543202478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584546 | AGAAGATGAGACACG[C/T]CCATTTTTAGGCATA | 7347 |
rs543212990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581162 | TTTTAACTATCTACC[C/T]ACTAATGATCCCTTC | 7347 |
rs543221041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554237 | CGGCTAATTTTTGTA[C/T]TTTTTGTAGAGACAA | 7347 |
rs543249624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605432 | AGATTTGCTTGAACC[C/T]GGAAGGCAGAGGTTG | 7347 |
rs543261473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576290 | GCTGGAGTGTAGTGG[C/T]GCAATCTCTGCTCAC | 7347 |
rs543327344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547103 | TGTGTATTTTCTCTG[C/T]AAGGCACATGAAAGC | 7347 |
rs543438063 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560608 | TACTGAATGTCAGTT[A/G]CATTTGTATTTTATC | 7347 |
rs543454028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555583 | CTAGTTCAATGAGCA[A/G]CATTCTATCTCTTAA | 7347 |
rs543493167 | snp | C/T | 3.30196e-05 | 0.00406309 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569454 | ATACCTTTATTCTTA[C/T]TACAGGCCATCCGAG | 7347 |
rs543542926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576344 | AAGCAATTCTCCTGC[C/G]TCAGCCTCTCAAGTA | 7347 |
rs543804731 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548328 | GAAGAGGAGTTAAGG[G/T]AATGAAATACCTCTG | 7347 |
rs543864137 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550717 | TGTGCCTTATTTTAC[C/G]CTGTTTTTTTTTTTT | 7347 |
rs543945465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588809 | TATTACCATTCTTTT[C/T]ATTTCTTCTCACTAT | 7347 |
rs544046159 | snp | G/T | 0.000818163 | 0.0202092 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570247 | ACCACACTTTTTTTT[G/T]TTTTTTTTGAGACAG | 7347 |
rs544082700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555017 | TTCTGTTCTTGCATT[A/G]GTTTGCTAAGGATAA | 7347 |
rs544155670 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570946 | TTGGTTGCTCTAGGC[A/C/G]CTGCTTTCAAAGGTG | 7347 |
rs544162747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551324 | TAATCCCGGGTACTT[C/G]GGAGGCTGAGGCAGG | 7347 |
rs544326098 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568008 | GGTTTAAAGGTAGAC[A/C]TTAGACCATACTGTA | 7347 |
rs544333615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596213 | TGGCCCTATCAAAGG[A/G]GACAAGGAAAAGAAA | 7347 |
rs544405992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559939 | TGTGATAGATTAAGG[A/T]CTGACATTTTATTTT | 7347 |
rs544436201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573798 | TCAACGTATGAATTT[A/G]GCAGGGGGGACACAA | 7347 |
rs544465691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581430 | TCTTGGCTCCCTGTA[A/G]CCTTGATCTCCTGGG | 7347 |
rs544655213 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573355 | CTGTTTGTATTCCAG[C/T]CTACTGATTTTTTTG | 7347 |
rs544683440 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554253 | TTTTTGTAGAGACAA[C/G]ATGGTTTTACTCTGT | 7347 |
rs544775739 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589494 | GTTGGCTTTTTTTTT[C/T]TTCTTGGAGCTTATT | 7347 |
rs544778034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597506 | AGAAAATAAATACCA[A/G]TACAACAATAAAAAA | 7347 |
rs544868901 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581098 | TACCCATAAACCAGC[-/CA]CAGTCTTTTGGTAAT | 7347 |
rs544933474 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552423 | ATTGCATGTGTTGTT[A/G]TTATAATCAATGTGA | 7347 |
rs544936642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582097 | GTTATGTGGCTTTGG[A/G]CAAGTCAAGTAGGTC | 7347 |
rs544979170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596579 | GCCAGAGCAAACATA[C/T]GTAGGATTCATAACC | 7347 |
rs544991817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552352 | TCCCACTCTCTTTTA[C/T]TTCCTCAACCTAATG | 7347 |
rs545014267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75604059 | AATTTTTATTATGGT[C/T]AGAAACCATGGAATC | 7347 |
rs545026212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561056 | CCACCTTAGCCTTTC[A/G]AGTAGCTGGGACCAC | 7347 |
rs545089974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590020 | ACCATGCATCCCTGC[C/T]CTGGGTCAAACGTAA | 7347 |
rs545097463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554337 | TATAATCTCTTCTAA[C/T]CTTGTAAGATCACTA | 7347 |
rs545126712 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589610 | CATGGTTTTTGTGTG[A/T]GTGTTACTTTTTAAA | 7347 |
rs545162221 | in-del | -/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75546900 | AAATCGTTGCTTCTA[-/G]GGGAAATACAGGTTA | 7347 |
rs545247361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565928 | AGGCAGTCAGCTATA[C/G]AGCCCACATTTTTGA | 7347 |
rs545316836 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596700 | TCTCTAATGATCTCA[A/G]TGGGAAGGAAAGAGT | 7347 |
rs545357929 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558757 | GTTCTAGAAATATAC[C/G]TTGGGTGTCTGTGAT | 7347 |
rs545482425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557280 | GGTGAAGTGGGTACT[A/G]CTCCTAGCTCCTCAC | 7347 |
rs545535869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605578 | CAAATTAGGGCACCC[A/G]TGTTCACTTTTCTGG | 7347 |
rs545730976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572153 | CTATTCTTCTTGCAG[C/T]ACTCTCTTTCTGAAA | 7347 |
rs545732567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575670 | GTAGAGCTGGAATTT[A/G]AGCTGAAACCGTCTG | 7347 |
rs545768163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588471 | TATTAAACTATATCT[A/G]TGAGAGAAGACATTA | 7347 |
rs545797937 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572872 | GTGTCTCCCAGTTGC[C/T]GAGAGAACAAAAATC | 7347 |
rs545915434 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75604152 | TTATGGATTTGGATA[C/T]ATAATTGTCAGTTGA | 7347 |
rs546240783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574149 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 7347 |
rs546272757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594104 | TAGTTACTACATATC[A/G]TAGGAAGTGCCAGTT | 7347 |
rs546287575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557291 | TACTGCTCCTAGCTC[C/T]TCACATACAAGGGTC | 7347 |
rs546296322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586789 | TTCATGGATCAAAGA[A/G]GAATCACAAGAGAAA | 7347 |
rs546316327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581379 | CCTTGAGACAGGGTC[A/C]CATTCTGTTGCTCAG | 7347 |
rs546326672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550231 | ACGTATCTTGGGGAC[G/T]CCGGGTCTGAGGTTT | 7347 |
rs546345012 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550511 | CTTCCAGTCTTTTAA[A/C]GCTGGACATTTAGTT | 7347 |
rs546461097 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551239 | TCAGGAGTTCGAGAC[C/T]AGTCTGGCTGGTGAA | 7347 |
rs546462641 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563151 | TATGTATGTATGTAT[A/G]TATGTATGTATGTAT | 7347 |
rs546512822 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579155 | TCCTTTTGGAATTTA[C/T]TTCCTCTTCCTTCAT | 7347 |
rs546535462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556058 | GGTCATTGACTTTCA[G/T]AAAATATGCCTCCTA | 7347 |
rs546645259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587418 | AATTAAAATATGGGA[C/G]ATTAGGAGAAAGTAT | 7347 |
rs546652379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601254 | GATTACATAAATGTA[A/G]TTGATAAAGCAGCAG | 7347 |
rs546657200 | in-del | -/TATATATATATAT | 0.282369 | 0.247896 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592415 | TTTAATTTTTCCTTC[-/TATATATATATAT]ATATATATATATATA | 7347 |
rs546681998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594712 | GTGCTTTTAGTCACT[A/G]TTTTCTTTGCCGATA | 7347 |
rs546709062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602572 | GCATTTACTGAAATT[A/G]CACGCAAAGTTGTTG | 7347 |
rs546771855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580536 | TGCCATATTTTAGAC[G/T]CAGCGGTCTTGTCCT | 7347 |
rs546845560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573943 | ACTTTTCAGGCTGGG[C/T]GCGGTGGCTCACGCC | 7347 |
rs546920108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564121 | ATCTTGGCTATCCTG[A/G]GTAATGCTGCAGTGA | 7347 |
rs546933414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580821 | TCACACAGCTAGTAG[A/G]TACTCCTGTGCTCTT | 7347 |
rs547061762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569624 | GAAAGTTACTTGGCT[C/T]TTTGTTTTTTCCTTT | 7347 |
rs547077106 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597447 | ATTTGCTCTCTGTGG[G/T]TTCTTGCATTGGTAG | 7347 |
rs547110460 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606034 | CTTGTTTGAAAACTA[A/G]CAATAGCTTTCTTAT | 7347 |
rs547156034 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574011 | TCACAAGGTCAGGAG[-/A]TCGAGGCCATCCTGG | 7347 |
rs547344479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604478 | GGGGTGATAATTTTT[A/T]AAAAACTGACAATAA | 7347 |
rs547414245 | snp | C/T | | | missense | UCHL3 | GRCh38.p7 | 13:75566756 | GACAAGATGTTACAT[C/T]ATCAGTATATTTCAT | 7347 |
rs547482580 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587333 | GAGACATGATGAATA[A/C]ATTTAATATCTGTGC | 7347 |
rs547534721 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559078 | GGAGTCTGGCTCTGT[A/C]GCCCAGGCTGGAGTG | 7347 |
rs547641615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568579 | ATTACATACCAGTAA[C/G]TATATATTTGATATT | 7347 |
rs547676189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575950 | AGAGACGGGGTTTTG[C/T]CATGTTGGCTAGGCT | 7347 |
rs547782727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592147 | GTGACATTTATATTT[A/C]GTATTTAATTTATAT | 7347 |
rs547801484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592943 | AGCTCATTTAAACCT[C/T]GAGGTGGATAAGAAA | 7347 |
rs547806368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577493 | TCTGTGGATTTTGGT[A/G]TCTTCAGGGGGGTCC | 7347 |
rs547812938 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548371 | AGTGGCCAGAAGAAC[A/G]TGGGTGGGAGAGTTG | 7347 |
rs547842211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584958 | GGGGGAAAAACCACA[C/T]AAAACAAACAGTGCA | 7347 |
rs547895999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562325 | ATAATAGAGAAATTT[G/T]GAGTTAGGAATTTCT | 7347 |
rs548028781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555240 | TCAAGTTCAAGTCAT[C/T]TCATCAGTGAGTCTT | 7347 |
rs548034355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570785 | TGTGGTGGTGCATGC[A/C]CCTGTAGCACTAGCT | 7347 |
rs548120106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577191 | GGAGGTCAAGACTGC[A/G]GTGAGCTGTGATCAT | 7347 |
rs548242388 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564298 | TGGGACTACAGGTGC[C/T]TGCCACCACGCCCGG | 7347 |
rs548295744 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548479 | TCTATTAGGTGCAGA[A/G]TAGTAATATGCACTC | 7347 |
rs548420496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561844 | ACGTATATACGTATA[C/T]GTATACATACGTATA | 7347 |
rs548540944 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579539 | CTTTTCTCTCCCTCC[A/G]TCTGTCTTCCCTTCT | 7347 |
rs548557494 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75598955 | GACTCATGGATTCCT[A/G]CTTTACTTGAATGAT | 7347 |
rs548580918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571697 | TAGGGGTTTCCTAGT[A/G]TGTAGAGCAGTGATT | 7347 |
rs548707578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550278 | TGTATTCCTATTCCC[C/T]TTCCTTCTTCGTTTT | 7347 |
rs548864541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578570 | GACTGCAGCTTTGAA[A/G]ATCGCTTGCCAGTAT | 7347 |
rs548931831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547410 | TTAGCAAGTAGGCAG[A/G]TTCAAAATGCAAAAC | 7347 |
rs548978556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574670 | TAATGGGCATTCAAT[A/C]AATATTAGGCGGTAA | 7347 |
rs548982577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582389 | AGATGAGTTTATATT[C/T]CATGTAAAGTGGTGT | 7347 |
rs549018590 | snp | A/C | 0.000280285 | 0.0118349 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567352 | TCTCATGTGGGCAAA[A/C]GTTTGTGGGATTGTA | 7347 |
rs549180085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584128 | AACCACCCCTTTTGC[A/G]GGAGGGGCAGGTTCT | 7347 |
rs549218537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577132 | CCTGTAGTTCCAGCT[A/G]CTCTGTAGTTGGGAG | 7347 |
rs549219868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551611 | ATAAAAAGTAACATA[C/T]GACCAAGAGCAGTTT | 7347 |
rs549226683 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595772 | AGTTACTTGGTATTT[G/T]GGCTTATACCTGTAC | 7347 |
rs549270611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581863 | TTGGCCTTTGAGGAC[A/G]TAGGTGGTGATTGTT | 7347 |
rs549276194 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584271 | GCACCAAGAAACAGG[A/T]CTCAAATGTGTGGGG | 7347 |
rs549280418 | snp | C/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602201 | AAGCTCCATCATTCA[C/T]GTCGTTGGCCATTGT | 7347 |
rs549295814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553138 | ATAAATCATATAAAT[G/T]CTCATAAGAATTCTC | 7347 |
rs549397823 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598680 | TGCGTTCTTCTCAGT[G/T]CATCATATCGAGAGG | 7347 |
rs549435385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597937 | CCCTCCCTTTTCCTT[C/G]GGGCCTCATATAGTT | 7347 |
rs549560205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604500 | TGACAATAATTTTGC[A/G]TATTATTTTCAGGAA | 7347 |
rs549591892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596961 | TCAAGAAGAATGATC[C/T]GATGGAAAATTAGAA | 7347 |
rs549597142 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571358 | TTTTCAGACCTAACC[G/T]CCTTCATTCTTTCCA | 7347 |
rs549723457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605058 | GCAAGAATAGTATTG[A/G]AAGACTTGCTCATTA | 7347 |
rs549728845 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557713 | ATTTTGTGTTTTCTC[C/T]CAGTTTTGTAAATTT | 7347 |
rs549782684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583091 | TAGAGTAAAAATTTA[A/G]AATTATTGATTCTAA | 7347 |
rs549906506 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592496 | TCCCATCTATAGCCT[-/T]TTTTTTTTTTTTGCC | 7347 |
rs549941209 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568509 | TTTTTAAACAAGAAT[G/T]TGATCATACTGTAAT | 7347 |
rs550007695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584805 | GTAATGAAAAATACG[A/G]TACTAGAGATGAAGA | 7347 |
rs550048076 | snp | A/G | 0.000238521 | 0.010918 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560893 | AAAGGTAATTGTTAT[A/G]TAAAATAGAAAGTTT | 7347 |
rs550058570 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605900 | AATTTTGATATTTTC[A/G]TTAACTTGATGATTA | 7347 |
rs550147636 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561044 | CAAGCGATCCTCCCA[C/T]CTTAGCCTTTCGAGT | 7347 |
rs550187295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591994 | TTTGGAGCATTTGAG[A/T]TTTCAGATTTTTGGA | 7347 |
rs550234928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554502 | CTTCTTGCAAAGGCT[A/G]TTCCAAATACGGCTA | 7347 |
rs550348629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598246 | CAATTCATATTTCTG[A/C]GCCATTTGAAAATAA | 7347 |
rs550388107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605177 | TTAGAATCAATGAAA[C/T]GTGATTTTTAGTTGA | 7347 |
rs550401013 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583228 | AGTTTAAAAATAAAC[A/G]ATTACAATATATTGA | 7347 |
rs550404238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580563 | TCCTCTCCCTCTCCC[G/T]CTCCTCAAAATTGTT | 7347 |
rs550508914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75598913 | AGCTTTCCTTTTCCT[C/T]TCATTTATTCATTTA | 7347 |
rs550592782 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595632 | AAAAAAAAAAAGAGC[A/G]TAATAGTTGTAATGA | 7347 |
rs550662461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588204 | CTGAATTCTTTGCCA[A/G]GAATATTTTCCCATT | 7347 |
rs550738521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602033 | AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG | 7347 |
rs550814667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566294 | ATATGTAAATCTATT[A/G]TGCTTTATAGTATTC | 7347 |
rs550840076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550254 | TGAGGTTTGGAGGGA[C/T]TTTTACCCTGTATTC | 7347 |
rs550882845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557494 | TTGAGTTAGTCAGAG[A/G]TTTTTTTGGTTATTT | 7347 |
rs550902326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574399 | TAGAATGTAGGTCCC[A/G]TGAGGAAATAGGCCT | 7347 |
rs550902464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565508 | GTTTTCTATAGACAT[C/T]GTTTGTTTCTTTTAT | 7347 |
rs550905231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603381 | GTGCCTGCAGTCCCA[C/G]CTACTTGGGAAGCTG | 7347 |
rs550917195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601769 | TTTTTAGAAGTTTTA[A/G]TTTCTGTATAGTCTC | 7347 |
rs550944938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558447 | GTTTGCAGCACAGAT[G/T]TAAAATTGCTCTGTT | 7347 |
rs550951353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591224 | TATCTTTCCTTAAAT[A/G]TTTGCTTCCACCAAA | 7347 |
rs550965009 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559121 | CTCTGCTCACTGCAA[A/G]CTCCGCCTCCCGGGT | 7347 |
rs551095061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576115 | AGACCAGTGTTTTAT[A/G]TTAGGCTTAATGTGA | 7347 |
rs551120531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596263 | ATGTGCAACCCTGAG[C/T]GTTGTCTACAATACT | 7347 |
rs551158525 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548281 | AAGCCAAAGTGTTAG[A/G]TGAGTATAGCAGCAA | 7347 |
rs551181467 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548483 | TTAGGTGCAGAATAG[C/T]AATATGCACTCTTCC | 7347 |
rs551196457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574009 | GATCACAAGGTCAGG[A/G]GATCGAGGCCATCCT | 7347 |
rs551267444 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584103 | CTTTCCTGGGGAAGG[A/G]AAGAGATAAAACCAC | 7347 |
rs551385372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552864 | TTTGTGATTTGAGTA[C/T]AGTACAACCACATTA | 7347 |
rs551387926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588875 | AATTTTTTATTTTAT[A/G]TACTGGTGTTATTAA | 7347 |
rs551427764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574572 | CTTCAGCACAAAATA[G/T]AAATAATGGCATTTA | 7347 |
rs551477704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589807 | CATACATGATCCTTT[G/T]CTAGATAGATTATGG | 7347 |
rs551496181 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553649 | GTAATGTTTTCTGTT[G/T]TATAGTTCTAATACC | 7347 |
rs551504106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581782 | ATTTAAAAGTTTAAA[G/T]AGTAATTTATTCATT | 7347 |
rs551509320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602417 | TCTTCCCCGTCCAGC[C/T]TGGAAGTGGCACAGC | 7347 |
rs551598863 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595420 | CTGACCAACATGGAG[A/G]AACCCCATCTCTACT | 7347 |
rs551624653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558160 | TGAATTTCTTTATAT[C/T]TATCTCATTTAATTG | 7347 |
rs551657908 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566989 | TGATGGGAATGTATA[C/T]ACTGTTAGAAGAAAT | 7347 |
rs551668201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575173 | GTCACCAAAATACAG[C/T]AGTCTTTTTCAGAAG | 7347 |
rs551672092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595680 | AGTTTTCAGGGTTTT[A/G]TAATGTTCCTGTGAT | 7347 |
rs551688122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550889 | TAGCAAATTCCCTGG[A/G]CAAAGAGACATCCTC | 7347 |
rs551702126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559273 | TCTCGATCTCCTGAC[C/T]TCGTGATCCACCCGC | 7347 |
rs551842647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600610 | CTTAAGCCCTCTGTT[C/G]AGACGTACTGCTCAG | 7347 |
rs551880081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556645 | ATTTAGGGACAGGAA[C/T]GAACAGGTTTTTAAG | 7347 |
rs551911129 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583079 | AATAAGTCTGACTAG[A/G]GTAAAAATTTAGAAT | 7347 |
rs551941171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570813 | GCTACTAGGGAGGCT[G/T]AGGTGGGAGGATTAC | 7347 |
rs552120652 | in-del | -/TGTGTG | 0.00270635 | 0.0366859 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563921 | GCCGAATAATATTTC[-/TGTGTG]TGTGTGTGTGTGTGT | 7347 |
rs552179832 | in-del | -/TAG | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567143 | ATTTAACCTGAAAAA[-/TAG]TAGCATACTTCTAGT | 7347 |
rs552262388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601134 | CAAGTAAGGAGTTGC[C/T]TCTTAAAGATGAGCA | 7347 |
rs552274409 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558915 | GACTAGGAAGCTTGC[A/C]GGAAGTGGAGAAAGG | 7347 |
rs552325646 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589186 | CTGTTACCTACTGGC[A/G]ATGTGACCTTGGTTA | 7347 |
rs552336697 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553811 | GCCAAAAAAGAAATA[C/T]GGGTTTTCATCTTCC | 7347 |
rs552380379 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593949 | AGGATATTAAGTAAT[A/C]TGAGATATAATTTGA | 7347 |
rs552382304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586041 | ATGTCAGTATAAAGA[A/C]TCAAATGTCTATAAA | 7347 |
rs552409615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555427 | AGGGATGCGTCTGAA[A/G]TATGAGAACGGTGCC | 7347 |
rs552528447 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573272 | TCTGTCTCAGAAAAA[A/C]AAAAAAAAAAAAGAT | 7347 |
rs552583324 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585323 | CCACATGAAAAAGAC[A/C]GAGTAGATACTAAGA | 7347 |
rs552591802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564219 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 7347 |
rs552733006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555487 | GTTGTCAGATGGAAG[A/T]ATGAATAGATCTTAT | 7347 |
rs552754250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564614 | GCATTCCCACCAACA[A/G]TGCACTTGGGTTCCC | 7347 |
rs552759822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571825 | ATCTCCCACAGTTTA[C/G]AAACACTACTGGAGT | 7347 |
rs552809726 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549502 | GCGTAGAACGCGAGC[G/T]CTCGGCAAGGCTCGG | 7347 |
rs552849799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599992 | TGAACACATGAATGA[C/T]GAGAAAGCAAAACAG | 7347 |
rs552967293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593211 | CTCTTTCCTAGGTGA[A/G]TGAATAATTCATTAT | 7347 |
rs552998785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601460 | CGCCGTCCTGATCAG[G/T]CAGGAGATATCAACA | 7347 |
rs553013326 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592505 | TAGCCTTTTTTTTTT[A/T]TTTGCCCTTTGTGTA | 7347 |
rs553130992 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574786 | CTTGGATTTTATAGA[A/T]GGAGAACCACCAAAG | 7347 |
rs553251400 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600686 | TGTAATCCAAGAAGT[C/G]CGATATAGATATATT | 7347 |
rs553272842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563575 | AAAATAGTTACAATA[A/G]TGAAGCAGATTAATA | 7347 |
rs553311095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605273 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 7347 |
rs553392304 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568236 | TCTTTGAAATTAGGC[A/G]TATAATCTACAAATT | 7347 |
rs553397027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604657 | TAGGATATATTATTG[A/C]AAATGGCTTTTAACT | 7347 |
rs553532334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550390 | AGCTTTGTAAACTCG[C/T]CCACCCAGTCCTTGT | 7347 |
rs553581103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582640 | ATTCAAAAATAAACT[G/T]TAGACATTTAATCTT | 7347 |
rs553658087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557155 | AGGAATTAGAGGTTG[C/T]AGTGAGCTGTGATTG | 7347 |
rs553784853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561492 | CACATTTTGATTTAT[C/G]TGTTTTAGAAATTTT | 7347 |
rs553789395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567711 | TGGCACCACACCTGG[A/C]TAATTTTTGTATTTT | 7347 |
rs553802502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554905 | GATCCTCTCCTCAGC[C/T]TTCACCTTCAGGTAG | 7347 |
rs553853730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75590096 | TCGCTGGCGACCCTT[C/T]TTACGTCTACCATCT | 7347 |
rs553882214 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567994 | AAGGAGAAAGCAAAG[A/G]TTTAAAGGTAGACAT | 7347 |
rs553927686 | snp | A/G | 7.05803e-05 | 0.00594013 | missense | UCHL3 | GRCh38.p7 | 13:75566713 | GAAGTATTCAGAACA[A/G]AAGAGGAAGAAAAAA | 7347 |
rs553954572 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554168 | CCTGGGCTCAAGCAC[G/T]CCTCACACCTCAGCC | 7347 |
rs554071082 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587105 | AAGTCAATGAAATTC[A/G]TTACTGTAGTAGAGG | 7347 |
rs554080686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560609 | ACTGAATGTCAGTTA[C/T]ATTTGTATTTTATCC | 7347 |
rs554104506 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599125 | AGGCCTGTGCCACCA[G/T]GCCTGGCTATTTTTT | 7347 |
rs554130452 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559696 | GAAATGCCTATGGCA[C/T]CTTTTTTGTTTGTTT | 7347 |
rs554183843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598437 | CTGATTATCACAATA[A/T]TGTCCTCTATTCAGG | 7347 |
rs554192114 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606141 | ATCTATGTTAACATG[C/T]TTATTTAGAAAACAT | 7347 |
rs554209223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562553 | AAAAAAATCAGTTGC[C/T]TAAAGCTTAGGGTTT | 7347 |
rs554295442 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606309 | AATACCAATGATAGA[C/T]GCTGTGTGGAGAATT | 7347 |
rs554320784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569012 | GTTGTGCTCCACATT[A/T]CTCAATTGCTGACTG | 7347 |
rs554403437 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590202 | TTTTTTTCTTAACTT[C/T]GGTCTTCAGAGTGCT | 7347 |
rs554470523 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561873 | TACATATATACATAC[A/G]TATATACGTATACAT | 7347 |
rs554501257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590993 | GACTGTGGTTTGGCA[A/G]AGCCTCCCTAGAAAT | 7347 |
rs554518576 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554186 | TCACACCTCAGCCTT[C/G]CAAGTAGGTAGGATA | 7347 |
rs554544511 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577442 | TACATAGGTTATATG[C/T]AAATACAACACTATT | 7347 |
rs554598982 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548891 | TCTTGACCGGGTTGC[C/T]TCTGTTTACCTCTAC | 7347 |
rs554697885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596200 | TATTAAAAAGAAATG[A/G]CCCTATCAAAGGGGA | 7347 |
rs554731094 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548006 | AACTGTCTTGCTGTC[C/T]GGCCTTGTGTCTCAG | 7347 |
rs554804495 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555510 | GATCTTATAAAGCTG[C/G]TTTCCTGCTCCAGAA | 7347 |
rs554902362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584504 | CTCTTGACTAGGTTG[G/T]CTTATCCCCATACAC | 7347 |
rs554997573 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562505 | AGATAACTATTCCAG[A/G]ACCCCAGTTGTAATG | 7347 |
rs555064047 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584773 | TTAACATAAGAAAGA[A/G]TCAAATGGAAATGCC | 7347 |
rs555083133 | snp | C/T | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563242 | GTGCAGTGGTGCGAT[C/T]TCAGTTCATTGCAAC | 7347 |
rs555125331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559329 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCCTCAG | 7347 |
rs555212985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566443 | CATATGCCCTGTAAC[A/G]TGATCGTACAAATAC | 7347 |
rs555302310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570144 | AAAAGAATTTAACTA[A/C]AGCTGTTTGGTATGT | 7347 |
rs555302375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577610 | TGGCAGGAAGTTCCA[A/G]TTTCATATGGTTTGG | 7347 |
rs555371025 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581003 | AGTTGTGCCGAATAC[G/T]TTGTTCTTTTTTGCC | 7347 |
rs555371438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571014 | ACACATAAGAGGCCC[A/G]TCTAAAAGTTTTTAA | 7347 |
rs555399105 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563215 | GCATCTCACTCTGTC[A/G]CCCAATCTGGAGTGC | 7347 |
rs555442240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575506 | AAAATAGTGTTATTA[C/G]AGTTGCTACAGAAGT | 7347 |
rs555474517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582800 | TATTATAAGGATTTA[A/G]AAGTTGGTGTATGTA | 7347 |
rs555481021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558570 | ATGATACTTTTCCTT[A/G]AAAGGCAATTTAGGT | 7347 |
rs555486184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602996 | TTATTATGTTATTAT[C/T]TTATTTTTTTAGAGA | 7347 |
rs555512988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589842 | TAAAAATAGTAGACC[A/C]TATGAATTACAAGCA | 7347 |
rs555571092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587828 | CTTAAGGGATGAGGT[A/C]ATGTCTTTGCCTCTG | 7347 |
rs555591801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580707 | GGGCAGGCTAACTAA[A/G]TGCTGTATCTACCCT | 7347 |
rs555708044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581125 | GTAATCATGTTAGGT[A/G]TATTTTAGAAAACAG | 7347 |
rs555786150 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593236 | CATTATAGCCTTTTT[A/T]ATTATAGAATTAAAG | 7347 |
rs555945516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553156 | CATAAGAATTCTCTA[A/T]TTAGTAGATACCATT | 7347 |
rs556035761 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551608 | TATATAAAAAGTAAC[-/AT]ATGACCAAGAGCAGT | 7347 |
rs556050507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589374 | CTAAAAGATAGCTAA[A/G]AGGCCATGATATTTT | 7347 |
rs556072450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581966 | AAATAGTAATAGATG[C/T]GCCCTTATGAATCAG | 7347 |
rs556093521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603967 | ACTTTTTATGGAGAT[G/T]AATTTATGTGTTGAT | 7347 |
rs556110092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559475 | AACCTTATTTTTGAC[C/T]AATGATATCATTAGC | 7347 |
rs556126759 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593104 | AGAGATGGTGTTAAG[A/G]TAACTAATAATTTAT | 7347 |
rs556174116 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559206 | ACCACGCCCAGCTAA[-/T]TTTTTTTGTATTTTT | 7347 |
rs556211714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570027 | CTTTTTTCATTTTTT[G/T]GTTTCTTCATTTTTC | 7347 |
rs556213844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561571 | AAGGAATCTTCTTTG[C/T]TTATTTTAAGTTGGT | 7347 |
rs556248616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569220 | TTAGAGCCTGGAAAT[C/T]ACAAATAATCAGATA | 7347 |
rs556393364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574121 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 7347 |
rs556432726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590823 | CTAATGATATCTGCA[A/T]ACTATTAAAAATACA | 7347 |
rs556471379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566585 | TCTTTTATTTTAAAC[C/T]CTTTCTTTCATAATA | 7347 |
rs556604090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564275 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7347 |
rs556649754 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553130 | CACAATAAATAAATC[A/C]TATAAATTCTCATAA | 7347 |
rs556655509 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576908 | TGTATACAGTTGGCC[C/T]GCTGTAATGGTGGGT | 7347 |
rs556746768 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75589969 | CATCACAGCCTCATT[C/T]TAGCCACTGCAGAAC | 7347 |
rs556755792 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549539 | AGAGTCCAAGCGTGA[G/T]GGGAGAGGGCTGTGG | 7347 |
rs556805391 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569142 | GCTTACTTTATTCTA[G/T]TCTCAATTGAATAAA | 7347 |
rs556831894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582926 | TATTGCTTGAAAGTC[C/T]TTTTCTGAATTAGAT | 7347 |
rs556942369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586897 | AATCTATAGCATGAA[A/G]TGCTTATAGTAGAAA | 7347 |
rs556974576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595206 | CAAAAATGTTTGCAT[A/G]CCATCTTCGCATTTT | 7347 |
rs557234473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600753 | GCATCCATTCTGCAG[C/T]CCATGGATCAAGGAA | 7347 |
rs557306349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594248 | GTTTGTTAAGCATCA[A/G]AGCAAGAGAAAAATC | 7347 |
rs557369538 | in-del | -/CTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572194 | CCTCAATCTCTTGCA[-/CTT]CTTCTATCCATTCTT | 7347 |
rs557402093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557751 | ATACATATGTGTATC[A/G]GTTCTATAGATTTGT | 7347 |
rs557437302 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564943 | TCAGATGATCCACCC[A/C]CTTCAGCCTCCCAAA | 7347 |
rs557442393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588404 | TCCCCTATTCTTTCC[G/T]TCTCTCTTTCCTGTT | 7347 |
rs557500716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572979 | CATTTAAGATTCATC[C/T]CCCTGCCGGGCATGG | 7347 |
rs557539745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565625 | TTTGACTTTGCCTTG[C/T]AAACAGCCATAGACA | 7347 |
rs557676616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557627 | TAGAGATGGCTTTGC[A/C]AATGCATGTATAGAT | 7347 |
rs557685935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589201 | AATGTGACCTTGGTT[A/G]TGTTACTTAACCCAT | 7347 |
rs557724686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581394 | CCATTCTGTTGCTCA[A/G]GCGGCAGTGCAGTGG | 7347 |
rs557731348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573559 | CCTGGCTTGTAGACT[A/G]CCACCTTCTCACTGT | 7347 |
rs557768105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580594 | CGAGGTGCTCACCAG[C/T]TTTCAAGTATTCTCA | 7347 |
rs557797782 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594673 | ACAATTTTTGGTCTT[C/T]AGATAGTTGAGATTA | 7347 |
rs557849221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582009 | ACAGTTGATGGGCGA[A/G]TGACCTTGCAATGGA | 7347 |
rs557940699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586939 | ACAGAGGTTAGAGGG[A/G]AACTATAGTATTACA | 7347 |
rs557992854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551875 | TGAACAGGAGCTGGT[C/G]ATTCTTTGGTGATTA | 7347 |
rs558054996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550513 | TCCAGTCTTTTAAAG[C/G]TGGACATTTAGTTGC | 7347 |
rs558084884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584549 | AGATGAGACACGCCC[A/G]TTTTTAGGCATACAT | 7347 |
rs558098822 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568677 | TAATAGTTTTTCTTC[C/T]TTTTCACTATTTTAA | 7347 |
rs558114107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602066 | GTGAGCTGAGATTGT[A/G]CCACTGTACTCTAGC | 7347 |
rs558170978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591793 | ATATTACGTACCTTA[C/T]TGGGTTTATACAGGT | 7347 |
rs558290423 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602858 | AAAATAGACTGTACG[G/T]TTTTGACATTTCAGG | 7347 |
rs558478435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551169 | GCGCGGTGGCTCACG[C/G]CTGTAATCCTAGCAC | 7347 |
rs558502316 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575345 | ATTGCTTTCATCTTT[C/T]GCTTAAGATTAAAAA | 7347 |
rs558530973 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548173 | AGCAGCCCCTGGCAT[A/G]CACTGAGTCCAGCAG | 7347 |
rs558544750 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548715 | ACCGAGCATTTTCTA[C/T]GTATCATGCACTGGG | 7347 |
rs558563776 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584315 | ATGGAGAGAGACCTT[C/T]TCTGAGGCATAGCCT | 7347 |
rs558578004 | in-del | -/TATATCTATT | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600563 | GAGCCGGGATGATAG[-/TATATCTATT]TATAGCCTGGATTAC | 7347 |
rs558627617 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554764 | CTTTTTTGTTTTTTT[A/T]AACTTTTAGCTTCAG | 7347 |
rs558646242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600968 | TGAGTTTGGAATAAG[C/T]TGGTTCCAATCCTCA | 7347 |
rs558704320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554288 | CAGGCTGGTCTCAAA[C/T]GCCTGGCCTCAAACA | 7347 |
rs558720942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605456 | GAGGTTGCAGTGGGC[C/T]GAGATTGCACCACTG | 7347 |
rs558816078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561947 | CTTTTAAGTGCATTT[C/T]ATAATAGATTTTGAG | 7347 |
rs558827747 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549558 | AGAGGGCTGTGGATT[C/T]AGATACTGTTTTTCT | 7347 |
rs558880522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570990 | TTGACTAAGTTTATC[C/T]ATACACAGACACATA | 7347 |
rs558906215 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595818 | GTTTACCTTTCAGTG[A/G]ACTATTTCATGGCAT | 7347 |
rs558913736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596550 | ATTCTGTTAACTTCA[A/G]GAAAGTAGATTTGGC | 7347 |
rs559082369 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584080 | CTAAAGACCTTGAGA[C/G/T]AGAAAACCTTTCCTG | 7347 |
rs559187877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562149 | GATTTAAGACTTTGC[G/T]TAGTCCTGGAAATTC | 7347 |
rs559267710 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602829 | ATTAATCTTTGTTCT[A/G]TACTGCTATTATAAA | 7347 |
rs559268012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563301 | CTGCCTCAGTCTCTG[G/T]AGTAGCTGGGATTTC | 7347 |
rs559300179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562802 | TTCTAAAGTATTTGC[A/G]TAAGTAAATTTGTAC | 7347 |
rs559403870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571164 | ATGATGAGGATCAGC[A/G]TAAGTTTATTGTTAA | 7347 |
rs559492466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600418 | AGCTTCAAAGGACAG[A/G]CTGATTGTCTTGTTA | 7347 |
rs559604500 | snp | C/G | 0 | 0 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601067 | AAACTAGAATTAGAA[C/G]GGGAGCCTGAAGATG | 7347 |
rs559614800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587039 | AAAAAAAAAAAAGAG[C/G]AAATTAAATCCAAAA | 7347 |
rs559783895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592965 | GATAAGAAACCCAAG[A/G]CTTACAGGGATTGGG | 7347 |
rs559937796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596718 | GGAAGGAAAGAGTTA[C/T]CTTAAAAAAAAACTC | 7347 |
rs560127877 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549317 | CCGACAAACGAACAA[C/T]AGCACCGTGCTGCAC | 7347 |
rs560132013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556407 | TGGCAGTAATATCAA[C/G]TAATTGCTAGGTAAG | 7347 |
rs560147631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589619 | TGTGTGTGTGTTACT[C/T]TTTAAAAACATTTTG | 7347 |
rs560267819 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75601148 | CTTCTTAAAGATGAG[A/C]AAATAAACTGATTTC | 7347 |
rs560269418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603294 | TATTAGCTCTTTAGT[C/T]TCATGAATGACACAC | 7347 |
rs560310855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582312 | AAAACATTTAATCTG[C/T]ATTTTAAAATTCCTC | 7347 |
rs560336141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547259 | CTCTCGTTTCCAGTA[C/T]AAGAGCTGCAAGAAG | 7347 |
rs560353136 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593396 | ACTCATTATCACTGT[C/G]TTCACATATTTAAAG | 7347 |
rs560368188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558864 | AATTTTTATCCTTTT[C/T]GGTTTTTAGATAGAA | 7347 |
rs560512650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575774 | TTTTGTTTTTTGAGA[C/T]GTAGTCTTGCTCTGT | 7347 |
rs560513701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597922 | TCTCTTTTGTTATCA[C/T]CCTCCCTTTTCCTTG | 7347 |
rs560517692 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561630 | ATTTTCAAAATAAAC[G/T]TGAATGGGAATCACT | 7347 |
rs560547749 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579026 | TCATTTTACTCTGAA[A/G]TATAGTTTTTAGTTA | 7347 |
rs560672739 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583066 | ATGAGGAGGTAAAAA[A/T]AAGTCTGACTAGAGT | 7347 |
rs560676668 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564296 | GCTGGGACTACAGGT[A/G]CCTGCCACCACGCCC | 7347 |
rs560700737 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582965 | TGAAATTGAAAATAT[A/C]TATGATGTACACTGT | 7347 |
rs560714060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604715 | AATGGAAGTTGAAAG[C/T]ACATTATCCTGTAAA | 7347 |
rs560714340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596756 | CTAGTTAGAGAGCTG[C/T]CTTGGCTCAGAGGCT | 7347 |
rs560777304 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555694 | AACTTTCTCCAGTTG[A/T]CTATCATTCTCATTG | 7347 |
rs560806276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569370 | TGTTTCTTTAGAAGA[C/T]TTTAGGTGTTAAAAT | 7347 |
rs560826907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597707 | TGAGATGGGGCCGGT[A/G]TCCTGGAACCAGTCC | 7347 |
rs561063545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583919 | GGAGAGCTCATATCC[A/G]CTCTCTGCAGACCTC | 7347 |
rs561237380 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552845 | TCTTCATTGTGATTA[-/T]TTTTTTGTGATTTGA | 7347 |
rs561312527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555013 | GGTTTTCTGTTCTTG[A/C]ATTAGTTTGCTAAGG | 7347 |
rs561336796 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606394 | AGGGAGGCTTCTGTG[A/T]GGAGGTGACTTTAAA | 7347 |
rs561346110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591970 | GTTGGTGCTCAAAAA[A/G]TTTGAGGTTTTGGAG | 7347 |
rs561388658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554458 | TTTCTCATTCCTCAG[A/G]TCTAATTGATCTGCA | 7347 |
rs561460296 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575440 | TTTCTTTTTTTCCAT[G/T]GATTTTCCACTTGCT | 7347 |
rs561491928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576311 | CTCTGCTCACTGCAA[C/T]GTCTGCCTCCCAGGT | 7347 |
rs561501724 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568484 | GGGAGTGTATATATA[G/T]ATACACAATTTTTTA | 7347 |
rs561502180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557948 | TTAATTGTAAAAGTA[A/G]GACATTTTAATGATT | 7347 |
rs561552308 | snp | C/T | 3.30447e-05 | 0.00406464 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605764 | GAAGTTTATGGAGCG[C/T]GACCCTGATGAACTA | 7347 |
rs561640591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602222 | TGGCCATTGTTGGGT[A/G]TTTGACAGTAGCTGA | 7347 |
rs561729908 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569978 | CCCTGTTAGCTAGTT[C/T]AGCTGGGTTGCTTTT | 7347 |
rs561730667 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557188 | GTCACTGCACTCCAG[C/T]CTGGGCAATGGAGCA | 7347 |
rs561735174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574911 | TTTGGTATTTGGGTA[A/G]TAGTTAGAACCCTGA | 7347 |
rs561808074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595505 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACA | 7347 |
rs561853351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573041 | AGGCCAAGGCAGGCG[G/T]ATCACCTGAGTTCAG | 7347 |
rs561891989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572429 | GTCATAGTTTACTTG[A/G]CGTTATTCCCATCTT | 7347 |
rs561908055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580859 | CAAAACGTGTAGGTA[A/G]TACAAATTGCTGAAA | 7347 |
rs562003980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559808 | TGATTTTTGTTTCCT[C/T]TATTCCTTTTTTCTA | 7347 |
rs562044411 | snp | C/G/T | 5.19344e-05 | 0.00509558 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566883 | TACTGCATTTTTTCC[C/G/T]CCTTAAGATACAAGT | 7347 |
rs562102781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566107 | CGTAACAATTAGCAA[C/G]TAAAAGTTCTCCAGT | 7347 |
rs562265498 | in-del | -/TAGAGAA | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556769 | TCATTGTGGCCAAGT[-/TAGAGAA]TAAAGTACCAAAAAG | 7347 |
rs562349038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603069 | ATCATAGCTTGCTGC[A/G]TCCTTGAACTCCTGG | 7347 |
rs562421784 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566914 | TAATTGCATTGAGCA[A/G]TAGGTGGTGCTCTAA | 7347 |
rs562437025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596226 | GGGGACAAGGAAAAG[A/C]AAGAACATAGTATTT | 7347 |
rs562709870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564568 | TCTTTAGAAATCTCC[A/G]TACTGTTTTTCATAA | 7347 |
rs562772736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550771 | CTTTTTTACTGCTCT[C/G]CTAGTTTATCATACT | 7347 |
rs562777663 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564075 | TGTTTTTATCCATTT[A/T]GCCATCTATGGACAT | 7347 |
rs562813589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558076 | GTATTCAGATAGCTT[C/T]TGGTGAGCCTGACTC | 7347 |
rs562816309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553618 | GCTCATCTTTTTTAT[A/G]TGTTTTCTTGCCCTA | 7347 |
rs562872499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604416 | ACTTGAGATCTTCCT[A/G]TTTAAAGTGAAAAAA | 7347 |
rs562941628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562994 | GCAAAGTTATTAAGA[A/G]GATATCTAGTGCATT | 7347 |
rs562943603 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572010 | CTTGTCTTGTCTTGT[C/G]TTGTCTTGTCTTGTC | 7347 |
rs563005600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552779 | ACATCAAGAATTACA[A/G]CATTTATAGAGTGTG | 7347 |
rs563066648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552516 | ACTATATGCAGATGA[A/G]TATTAATTGTTAGAC | 7347 |
rs563117310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589521 | TATTCCTTTTAAGGA[A/G]TTCTTTTTTACCAAT | 7347 |
rs563301453 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579407 | TTTGGAGGCGATTTT[A/T]TTTTATTTTATTTTT | 7347 |
rs563304058 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600615 | GCCCTCTGTTGAGAC[A/G]TACTGCTCAGAAAAA | 7347 |
rs563367963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556541 | AACAAATTTGAAAGG[A/C]AAGTGAATTTTATCT | 7347 |
rs563449330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75585771 | TGGGATAATACTGTT[G/T]TGAGGTTCTTATACT | 7347 |
rs563502095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582477 | TTCACTGTTAATGTC[C/T]TGGCAAACATTGGTG | 7347 |
rs563502880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601507 | CATCAGCAAAAAGAT[A/G]GCAACTTGCTGAAGG | 7347 |
rs563545832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75601120 | TGATAAAACTTGAAC[A/G]AGTAAGGAGTTGCTT | 7347 |
rs563615760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594613 | GCAATGTGCATATAC[A/T]GTATACCAGGCATTG | 7347 |
rs563623416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578118 | ACATTTTAAGAACAG[C/T]TGAGATCAAGCGATT | 7347 |
rs563736072 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556664 | CAGGTTTTTAAGACT[C/T]GTTTGTGTGTCTAGG | 7347 |
rs563736089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564372 | AGCTGGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 7347 |
rs563742640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587176 | AATATTGTTTAAAAA[A/G]GAAGAAGTAAAGCAG | 7347 |
rs563867101 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550129 | TCGGCTTTACGCGGG[C/T]CCGCCCCTTTCAGAA | 7347 |
rs564004717 | in-del | -/AGGTCAACAAATGCTGTGTACCTTCTG | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590476 | TCATTTAGTTGACTC[-/AGGTCAACAAATGCTGTGTACCTTCTG]AGTTCTTTGCCATCT | 7347 |
rs564113097 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588026 | TGCTATAAGTAATAA[-/T]TTTTTTTTTTCTCTG | 7347 |
rs564118622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571509 | TTACAATAGTTCCAC[C/T]ATACTTTTTCCCACT | 7347 |
rs564157192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578346 | ATCTAAGTATTCTTT[G/T]GGGTAGCTTCTTGTA | 7347 |
rs564180996 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550202 | CACTCCTCTGGTCCC[A/C]TTCTGCAGTCACCAC | 7347 |
rs564223050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577377 | TAACATTTACATTGT[A/G]TTAGGTATTACAAGT | 7347 |
rs564254405 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559833 | TTTCTATCATCTAAA[A/G]CTTATTTTGTAATGA | 7347 |
rs564260056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559079 | GAGTCTGGCTCTGTA[A/G]CCCAGGCTGGAGTGC | 7347 |
rs564426380 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572159 | TTCTTGCAGTACTCT[C/G]TTTCTGAAAATATTC | 7347 |
rs564429106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574176 | TGAGCCGAGATTGTG[C/G]CACTGTACTCCAGCC | 7347 |
rs564683533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576354 | CCTGCCTCAGCCTCT[C/G]AAGTAGCTGGGACTA | 7347 |
rs564741427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597787 | GTATGATTGTAGACA[A/T]TGTGCAAGTTAATTT | 7347 |
rs564865875 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582710 | CTAGCTCAAGATTCA[A/G]CTCACAGTTTAAATT | 7347 |
rs565011699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576896 | TTTAAAAATGAATGT[A/G]TACAGTTGGCCCGCT | 7347 |
rs565168301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583124 | TTTTAACATTTTGAC[A/T]TACTTGTTAGAAACA | 7347 |
rs565314362 | snp | C/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550360 | TGACTAATTTGCCCA[C/T]ACTTCCTGACTCCAA | 7347 |
rs565423190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599607 | GATCTTTGATATTAC[C/T]ACCGTAATTGTTTTG | 7347 |
rs565446522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555098 | TGCCCATCTCTGACC[C/T]GCTCATGCTGTGCTG | 7347 |
rs565472140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562049 | GAAGTAAATGGGAAG[A/G]TGTGAGAGAAATATG | 7347 |
rs565490000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575954 | ACGGGGTTTTGCCAT[A/G]TTGGCTAGGCTGATT | 7347 |
rs565505323 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587579 | TCAGGAAAAAAAGTT[A/G]TGTAGAAAAAGGAAA | 7347 |
rs565512108 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561808 | ATATGTATACGTATA[C/T]ATACGTATACGTATA | 7347 |
rs565530184 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577887 | TCCATATTAATTGAG[A/G]AGCCAGCCCAGATAT | 7347 |
rs565546379 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555584 | TAGTTCAATGAGCAG[C/G]ATTCTATCTCTTAAA | 7347 |
rs565576461 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575485 | GTACTTTATTCTAGA[G/T]AGAATAAAATAGTGT | 7347 |
rs565597901 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563580 | AGTTACAATAGTGAA[-/G]CAGATTAATATATCT | 7347 |
rs565627639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599075 | CTGGGCTCCAGCAAT[A/C]CCCTTGTCACAGCCT | 7347 |
rs565672668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584804 | AGTAATGAAAAATAC[A/G]GTACTAGAGATGAAG | 7347 |
rs565697262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569715 | TGTTAAGATGCTGCT[C/G]TCTGCTGTTTCAGTT | 7347 |
rs565748734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555293 | CCCCAAATCTGTACT[C/G]TCATCCTCACTTGTT | 7347 |
rs565850747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568632 | CATTATGTAGTATTG[C/T]ATTTCACCAATAAAT | 7347 |
rs565872470 | in-del | -/AACCACTTAATG | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576945 | CTTGTGGATTCAACC[-/AACCACTTAATG]AAAATATTTGAGGCT | 7347 |
rs566018074 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579733 | AAGAATGCTTTCAGC[A/G]ATAAAAATAGAACTG | 7347 |
rs566021943 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596026 | GTGAGTTTTGGTTCT[A/G]TTACCTCTCATTTGC | 7347 |
rs566030105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578400 | ATAAATATTTTTATG[A/G]TTCTTGTTAAATAAT | 7347 |
rs566055233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562598 | TACAAATAGGAGTTT[C/T]TTTGTCTGAATTGGA | 7347 |
rs566143529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591585 | TTTATATAATGTTGA[A/T]CTTGGCTCCATATTA | 7347 |
rs566176925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571584 | TGCTTTTTATGCAGA[G/T]TCTCAGTTTTTATTC | 7347 |
rs566240120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584402 | TACAACCCAACTTCC[A/C]CTCTAAGCACAAGGT | 7347 |
rs566273209 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599702 | TGCTCCATTAACCAG[A/C]CATTTCCCCATCTCT | 7347 |
rs566321047 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557440 | TTATTAATTATTTTT[-/C]TCAATTGGCCAAAAT | 7347 |
rs566336562 | in-del | -/C | 0.00443457 | 0.0468788 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577963 | TGTACTGCCCAGAAC[-/C]CCCCCCATGTAAATT | 7347 |
rs566389876 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564493 | GATTCATCTCCTTTA[C/G]AAGGTGATTGTCTCC | 7347 |
rs566408978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583961 | ATGAGATTAAGTGGG[A/G]ACAAGATGGGAGAGA | 7347 |
rs566416302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574013 | ACAAGGTCAGGAGAT[C/T]GAGGCCATCCTGGCT | 7347 |
rs566460434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574628 | ATGAGTTAATTATAT[A/G]AACTGCTTAGAATAG | 7347 |
rs566471567 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555227 | TGTCATCTGTGGCTC[A/G]AGTTCAAGTCATCTC | 7347 |
rs566520239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581031 | GCCGTTAACATCTAA[A/G]TCAGTTCTTATTCAG | 7347 |
rs566522657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595684 | TTCAGGGTTTTGTAA[C/T]GTTCCTGTGATTTTT | 7347 |
rs566612262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582697 | AAAAATTAGCCATCT[A/G]GCTCAAGATTCAGCT | 7347 |
rs566644854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587780 | CTGAAGTTGGAAATC[A/G]CATTTCTCACAGGTG | 7347 |
rs566647780 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558554 | TCTCTTATCAGGGTT[C/T]ATGATACTTTTCCTT | 7347 |
rs566758721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588312 | ATTTTTTTCTCCACT[A/G]TTTATTAGTCACCTC | 7347 |
rs566791062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552874 | GAGTACAGTACAACC[A/G]CATTATGTATATTTT | 7347 |
rs566829777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552029 | GAAAATGTAATACAT[A/G]GAATAGTGACAGGAG | 7347 |
rs566829861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560287 | CTCTCCTTAAAAACC[A/G]AGTGCTGGAAATGAG | 7347 |
rs566912758 | in-del | -/AC | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561807 | TATATGTATACGTAT[-/AC]ATACGTATACGTATA | 7347 |
rs566931062 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550615 | TTCTGGGTGTTGGAG[G/T]TTGGGGGTTGGGGAG | 7347 |
rs566981794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566380 | ATCTCCTACAAAGGA[A/G]ATTGCTTATTGGAGT | 7347 |
rs567030978 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551812 | GTGTCTTGAAAAACT[A/G]TCAAACACATTAATA | 7347 |
rs567126426 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600525 | TAAATCTTCTCTGCC[G/T]ATGTTCTATAAATGG | 7347 |
rs567151730 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596462 | CTGGAAGCAGATTTT[C/G]TACTCTGAATTGTGA | 7347 |
rs567206354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75603565 | TTTACTTATACTTTT[C/G]CCTTTATGTAAACAT | 7347 |
rs567232845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575246 | TTTCTCCATCCCACC[A/G]TGATTGTCTGGTAGA | 7347 |
rs567313401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589126 | ACCACAGTGATTAAG[A/T]TCATTGGACTCTAGA | 7347 |
rs567318630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574680 | TCAATAAATATTAGG[C/T]GGTAATTTTATTTTA | 7347 |
rs567406715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576037 | CATTACAGGTGTGAG[C/T]CACCGCCCCAGCCAA | 7347 |
rs567456637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588361 | TACATCATTTATTTC[C/T]CCTTTTTATTCATTG | 7347 |
rs567519446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583407 | TTAGAAAACATGATG[C/T]TCAAAAAGAAGGCTA | 7347 |
rs567616051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591349 | TCTTCATTTTTATTC[A/G]TTCATCCATTTGATA | 7347 |
rs567725728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584142 | CGGGAGGGGCAGGTT[C/T]TTCTACCACTGGAGG | 7347 |
rs567726127 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581710 | TTTTTTTTTTTTTTT[-/TA]AGTCTGGATCATTTC | 7347 |
rs567757077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553141 | AATCATATAAATTCT[C/T]ATAAGAATTCTCTAA | 7347 |
rs567797534 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567767 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 7347 |
rs567802972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579700 | ACACTTCCAGATCTG[A/G]CTAGATGAAACTCGT | 7347 |
rs567813095 | snp | A/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551132 | CAATTCTACATAAAC[A/G]TAAAAGAGGGGAGAC | 7347 |
rs567843144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584127 | AAACCACCCCTTTTG[C/T]GGGAGGGGCAGGTTC | 7347 |
rs567876004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604517 | ATTATTTTCAGGAAA[C/T]GAAAGCCAGCATTGT | 7347 |
rs567900230 | snp | A/C | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548522 | AATTTATGGAGTTAT[A/C]ATTGATAACTTCTGC | 7347 |
rs567952839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597973 | CATATGTAAAGGGGA[A/G]GAAGTACATATTTTA | 7347 |
rs567989924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605067 | GTATTGAAAGACTTG[C/T]TCATTATATCCGAGA | 7347 |
rs567989951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597237 | GTGGTGTGTTCCTGT[A/G]GTCCCACTTTCTGTA | 7347 |
rs568038278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587481 | GCACTGATATTAATG[C/T]AAGTTAATTCCCTTA | 7347 |
rs568049285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594131 | AGTTAATCAATGTAT[C/T]GACTTTGCATATGTT | 7347 |
rs568098091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584757 | GCAGAATTGGAAACT[A/G]TTAACATAAGAAAGA | 7347 |
rs568138374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565404 | AAATTCATATTTTGA[A/G]CACAGATACATTTGT | 7347 |
rs568150079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564133 | CTGAGTAATGCTGCA[A/G]TGAACATGGAAGTGC | 7347 |
rs568239846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602669 | AAAATTTTTCTGTGA[A/G]GGACCAAGTAGTAAA | 7347 |
rs568276425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573413 | TGCTGTCTGTATTAG[C/T]TTGCTTGGGCATTCA | 7347 |
rs568325528 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569981 | TGTTAGCTAGTTCAG[A/C]TGGGTTGCTTTTCCT | 7347 |
rs568354364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558419 | CACTAAAATATTCTA[A/G]CTGTGACTTTTAGTT | 7347 |
rs568428143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573944 | CTTTTCAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 7347 |
rs568571934 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553617 | TGCTCATCTTTTTTA[-/TG]TGTTTTCTTGCCCTA | 7347 |
rs568593628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573506 | GGAAATCCAACAGCA[A/G]AGTGTCAGCAGGGTT | 7347 |
rs568720734 | snp | C/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551291 | CAAAAATTAGACGGG[C/T]GTGGTGATACACTCC | 7347 |
rs568782284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554605 | GCTCCTAACTAGTTC[G/T]TCTGCTTCTCCTTTT | 7347 |
rs568839053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580977 | GTAATAAGTTACAAA[C/T]AGTCATTCAGAGTTG | 7347 |
rs568839337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588236 | CACCCATCCCAACTT[C/T]ATATATTCTTTCAGT | 7347 |
rs568874477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587628 | ATAAAGCAAATGGAA[A/G]TAAAATGTCATAGTC | 7347 |
rs568883022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596409 | CTGCAGAGATAAAGT[A/G]TAACAGTGATTGGGG | 7347 |
rs568941444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559125 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 7347 |
rs568992521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597056 | AATCTTTGAGATGTC[A/G]GAGCAATAATAGGTA | 7347 |
rs569027565 | snp | C/T | 1.64727e-05 | 0.00286986 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549978 | GTTTCGTTTTCAGGT[C/T]ACCAACCAGGTGAGT | 7347 |
rs569030740 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569165 | TGAATAAAGTGTTAA[A/G]TGTTAGTTCTAACAA | 7347 |
rs569064701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550272 | TTACCCTGTATTCCT[A/G]TTCCCCTTCCTTCTT | 7347 |
rs569065481 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565509 | TTTTCTATAGACATC[A/G]TTTGTTTCTTTTATT | 7347 |
rs569152691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75551800 | CTTGTTTCTAGGGTG[A/T]CTTGAAAAACTATCA | 7347 |
rs569228612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558474 | TGTTGTATGTACCAT[C/T]GTGTTTTATAACTTT | 7347 |
rs569230555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566325 | TATTACGATATGCCA[C/T]AATATATTTTAACCA | 7347 |
rs569269991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551134 | ATTCTACATAAACAT[A/G]AAAGAGGGGAGACGG | 7347 |
rs569280617 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574167 | AGCTTGCAGTGAGCC[A/G]AGATTGTGCCACTGT | 7347 |
rs569344828 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576160 | GCTTGGGATAGGAAA[C/G]AGATTGTGTGAGAAA | 7347 |
rs569395312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573988 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACAAGG | 7347 |
rs569406621 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548476 | TCCTCTATTAGGTGC[A/C]GAATAGTAATATGCA | 7347 |
rs569561684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576439 | TTTCACAGTGTTAGC[A/C]AGGATGGTCTCAATC | 7347 |
rs569587042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554643 | TAAAATCTAATTTCC[A/G]TATGCACCCAAAGTG | 7347 |
rs569600280 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580665 | ATTATTATAATGATG[G/T]TTACCATTTTCTGAA | 7347 |
rs569632952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555386 | TCATGTGTATCTTAC[C/T]ACTAGAATATAAGTT | 7347 |
rs569637532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570787 | TGGTGGTGCATGCAC[C/T]TGTAGCACTAGCTAC | 7347 |
rs569727245 | in-del | -/ATAA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603629 | GAATGTGATAGTCAT[-/ATAA]ACATAGAATAGTCTA | 7347 |
rs569739707 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549401 | AGAATAGGACTCCGC[A/G]GCACGCCTCCTAGCG | 7347 |
rs569876132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561849 | TATACGTATACGTAT[A/G]CATACGTATACATAT | 7347 |
rs569894543 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561600 | GTAGGGGAAACTGAT[A/T]ATGTAGGTTACATTA | 7347 |
rs569898750 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600219 | CATAACATAAAAGTG[C/T]ATGGTGAAGCAGCAT | 7347 |
rs569915555 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597897 | AACCAATGAAAAGGA[C/T]TGAGTTATTTCTCTT | 7347 |
rs569982718 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567578 | TTTGATATGCAGTCT[C/T]GCTCTGCCGCCCAGG | 7347 |
rs569997580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579583 | ATTTCTCTCCTTTCC[C/T]CCCCCCTTCTTTCTT | 7347 |
rs570023998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563281 | CCCAGGTACAAGTGA[C/T]TCTTCTGCCTCAGTC | 7347 |
rs570025823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572525 | ATCTCCCTTTCTGTG[A/G]CTCTTAGGCCTAGCA | 7347 |
rs570084067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593159 | AGAGTATTTCATATC[C/G]TGTTGGAAAATTGTC | 7347 |
rs570146911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555814 | CCCAGGCTGGCCTCC[A/G]GCTCCTGGGGTCAAA | 7347 |
rs570159069 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595591 | AACAGGAGTGATACT[A/C]CATCTCAAAAAAAAA | 7347 |
rs570184282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564199 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTGCG | 7347 |
rs570250294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591009 | AGCCTCCCTAGAAAT[A/G]GAATATCTTAAAGCT | 7347 |
rs570424309 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549465 | GGGTGACCACGCGGT[C/G]CCAGACCGGCGCAAG | 7347 |
rs570530353 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559101 | CTGGAGTGCAGTGGC[A/G]CAATCTCTGCTCACT | 7347 |
rs570530656 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589203 | TGTGACCTTGGTTAT[A/G]TTACTTAACCCATTT | 7347 |
rs570620677 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548721 | CATTTTCTATGTATC[A/C]TGCACTGGGTTAGGC | 7347 |
rs570651298 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587928 | TGTAACACAGCCTAT[A/T]CTTTTGCAACCATCC | 7347 |
rs570654533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599868 | CTTAGTGAGGAAGGC[A/G]TATTGAAAGCCAGGA | 7347 |
rs570689280 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568015 | AGGTAGACATTAGAC[C/T]ATACTGTAGCTATTT | 7347 |
rs570788270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573319 | GGCTTAAGAGTGTTC[A/G]GTGTATTATTATCTC | 7347 |
rs570816102 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553856 | ACCCTTTTCTTCCCC[A/G]TCTTCCAAGGGCATA | 7347 |
rs570826283 | snp | A/C | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606431 | ATCTGAATGACTAAG[A/C]CTGTCATAAAGGTGG | 7347 |
rs570853144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557026 | TTTCAGACCAGCTTG[C/G]GCAACATAGTGAGAC | 7347 |
rs570889086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550354 | TTTGGATGACTAATT[G/T]GCCCACACTTCCTGA | 7347 |
rs570889602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564220 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAAGCTC | 7347 |
rs570923908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601912 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACATGG | 7347 |
rs570961382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557553 | CAGAAGACTGGTGAT[A/G]GAGGTTATGAAACCT | 7347 |
rs570979092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579627 | AGAATTTTAGAAATG[A/G]AGATATTAAATTATT | 7347 |
rs570997228 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75578771 | ACCTATAAAAGAGGG[A/C]TTATTTGACCACTGG | 7347 |
rs571115524 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605687 | ATTTGTAAGTAAAAC[A/G]CTTTTACACTGAAAA | 7347 |
rs571139669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572613 | AAGTACAACATATGT[A/G]TATTAATTAACCAGA | 7347 |
rs571153859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589758 | CCTGATACTTGGTTA[C/T]ATATTTCCACTTTAC | 7347 |
rs571221306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560584 | ATATGTGCTGCTTTA[C/T]TGCATTCCTACTGAA | 7347 |
rs571264794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575932 | AATTTTTATATTTTT[A/T]GTAGAGACGGGGTTT | 7347 |
rs571309562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567640 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 7347 |
rs571334198 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553253 | AAACTTTCCACAAAG[-/A]ATTGTTCATAGCTGC | 7347 |
rs571338945 | in-del | -/TTTT | 0.00119737 | 0.0244387 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547318 | GGCTGGGAACTACAA[-/TTTT]TTGTCATCCTGTGAA | 7347 |
rs571387230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561385 | TATTTCTATTTTGAT[A/G]ACAGTAAAGTCCTAG | 7347 |
rs571433743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75575346 | TTGCTTTCATCTTTC[A/G]CTTAAGATTAAAAAC | 7347 |
rs571507229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576570 | AGTGTTAGCAAGGAT[G/T]GTCTCGATCTCCTGA | 7347 |
rs571626227 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589148 | GACTCTAGAACTTGA[-/T]TTCCTGGGTCTGAAT | 7347 |
rs571626839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584821 | TACTAGAGATGAAGA[A/C]TGCCATTAACAGATT | 7347 |
rs571668512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570029 | TTTTTCATTTTTTGG[A/T]TTCTTCATTTTTCCT | 7347 |
rs571673844 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597553 | CATAACAACTATTTA[C/T]ATAGCATTTATATTG | 7347 |
rs571713605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584276 | AAGAAACAGGTCTCA[A/C]ATGTGTGGGGATGGG | 7347 |
rs571781348 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554103 | TGTTCTATCTCCCAG[G/T]CAGGCTGGATTACAG | 7347 |
rs571807460 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554512 | AGGCTATTCCAAATA[C/T]GGCTATTCCAAATAT | 7347 |
rs571919472 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547647 | TACATCCATACCAGA[C/T]GGTGTAGGTTAAACT | 7347 |
rs571926465 | in-del | -/AGAA | 0.0023933 | 0.0345097 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557825 | AAAATACTAGAAAAT[-/AGAA]AGGTGGATTCACACC | 7347 |
rs571961516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604685 | ACTTTTCTTGCCTCA[A/C]TGGGGGAAGAGGAAA | 7347 |
rs572069534 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593471 | AATACAAGGAGACAT[A/G]TTTAGCCTCAGTATG | 7347 |
rs572098500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553337 | GCTTCTGTGTGTACC[A/G]TTTCGTAGTAACTTT | 7347 |
rs572108865 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574544 | CTGCTTATTAGCTTA[A/G]GCAGGATACTTTCTT | 7347 |
rs572133426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598299 | ATCTTTAAAACTTCG[G/T]TGTGTATTTTCTCAA | 7347 |
rs572159675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582983 | TGATGTACACTGTTA[A/T]GTCTATATTATGCAT | 7347 |
rs572185099 | snp | C/T | 3.36281e-05 | 0.00410036 | missense | UCHL3 | GRCh38.p7 | 13:75566845 | AATAAAGACAAGATG[C/T]ACTTTGGTAAATGAT | 7347 |
rs572222447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554993 | AGTGAGAACATGCGG[A/T]ATTTGGTTTTCTGTT | 7347 |
rs572320341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560689 | TAACACTATGTATAG[C/T]ATACTAGTTTTCTTT | 7347 |
rs572678554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583822 | GGGTAATGAAACAAA[A/G]TAGCTAAAAATTTTA | 7347 |
rs572690215 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571328 | ACTTCTTTTTAAATG[A/G]TCTTCATGTCTCTTT | 7347 |
rs572699830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564960 | TTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 7347 |
rs572753140 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549596 | TAGGAAATTGGCTTA[-/T]TTTTTTCTCCTCGGC | 7347 |
rs572790239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75573590 | AGCCTTACCTGGCCT[A/G]TCCTGTGTATTCATA | 7347 |
rs572849211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602190 | CTCTGTTTTTTAAGC[C/T]CCATCATTCACGTCG | 7347 |
rs572875640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582013 | TTGATGGGCGAGTGA[A/C]CTTGCAATGGAAAAC | 7347 |
rs573039188 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553694 | AGATGACCCCATGTT[C/T]CTTGAAACCCTAACA | 7347 |
rs573095176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551215 | CTGAGGTGGGCGGAT[C/T]ACCTGAGGTCAGGAG | 7347 |
rs573131491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550595 | TCTATAGCAATTTAA[A/G]TTCCTTCTGGGTGTT | 7347 |
rs573149133 | in-del | -/GC | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559098 | GGCTGGAGTGCAGTG[-/GC]GCGCAATCTCTGCTC | 7347 |
rs573231681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574857 | TTTTTTTGGGTCATA[G/T]GTGTAGGAGTCTAGA | 7347 |
rs573371746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75602903 | AATCTTAGTCTATAA[C/T]AATTGAAATTAATTA | 7347 |
rs573421322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551257 | TCTGGCTGGTGAAAC[C/T]CCGTCTCTGCTAAAA | 7347 |
rs573470104 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553159 | AAGAATTCTCTAATT[A/G]GTAGATACCATTTTA | 7347 |
rs573519320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558617 | TAATGAATGCTAGGG[G/T]TTTAGATTAGGAGCC | 7347 |
rs573552705 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603791 | TGTGTAATATAGTTA[C/T]AGGAAAATATTTCCT | 7347 |
rs573631153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557983 | TTTTTTTTGAAGACG[C/T]GAGTGGTAAAAGTTG | 7347 |
rs573695320 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598312 | CGGTGTGTATTTTCT[C/T]AAAACAAGTGGATAC | 7347 |
rs573702373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75559378 | CATGTGACTTGTTCC[A/C]AGAATGAACCTAATC | 7347 |
rs573866580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565219 | TCAAATCTTATTTTG[C/G]TTTGTCATCAGGAAC | 7347 |
rs573890771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580709 | GCAGGCTAACTAAGT[A/G]CTGTATCTACCCTAG | 7347 |
rs573932928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552120 | ATCTGGCATGCTTTG[A/G]CATGATTTAGTTTGT | 7347 |
rs574003187 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563229 | CGCCCAATCTGGAGT[A/G]CAGTGGTGCGATCTC | 7347 |
rs574067423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571251 | ACAAAAAATATTTAT[G/T]TTTGCCATACTTCTC | 7347 |
rs574182896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571908 | AAAAATGTTTGAGAA[C/T]GATTCCTCAAGCCTG | 7347 |
rs574243738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75582089 | ACTCACTAGTTATGT[A/G]GCTTTGGGCAAGTCA | 7347 |
rs574280971 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589434 | ATAGTTTATTCAGAT[A/C]GTCAGCTTTGGAGGA | 7347 |
rs574510994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601975 | TTAGCTGGGTGTGGT[A/G]GTGGGTGCCTGTAGT | 7347 |
rs574563197 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566093 | AACAATATAGAAACG[-/T]TAACAATTAGCAAGT | 7347 |
rs574704589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75592583 | TTTATTTATTTTTCT[C/T]GTTTTTAGTGGAATA | 7347 |
rs574741562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572711 | TTAGTTTTCTGTAGT[A/C]CCCCGAGTAAACAAA | 7347 |
rs574827000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587848 | CTTTGCCTCTGGAAC[A/G]AAGAGCCTGTTTGCT | 7347 |
rs574883530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550396 | GTAAACTCGCCCACC[C/T]AGTCCTTGTAATTTC | 7347 |
rs574896219 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564252 | GCCTCCTGGGTTCGC[A/G]CCATTCTCCCACCTC | 7347 |
rs574905463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75587047 | AAAAGAGCAAATTAA[A/G]TCCAAAATGCATAAA | 7347 |
rs574915490 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575293 | TCTGAACAGTAGCCC[C/T]ACCTCACTTATGCTT | 7347 |
rs574920382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550112 | TTGAGGGCCCCTCTT[G/T]TTCGGCTTTACGCGG | 7347 |
rs574936502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75572131 | TTATTTCCTTATTTT[A/T]TTATTTCTATTCTTC | 7347 |
rs574979711 | snp | C/T | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547082 | CTGAACAAACCTTAT[C/T]TAATATGTGTATTTT | 7347 |
rs575001348 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585230 | CACACATATATACCT[A/G]CTGAGATACATTAAA | 7347 |
rs575042213 | snp | A/G | | | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549441 | GACACTGCAAGAATG[A/G]GAAGGTGCGGGTGAC | 7347 |
rs575138143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75579872 | AGGAGAACTTTATTT[A/G]GGGCTACTCTCAAAC | 7347 |
rs575172406 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556665 | AGGTTTTTAAGACTC[A/G]TTTGTGTGTCTAGGT | 7347 |
rs575203228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75588421 | CTCTCTTTCCTGTTA[C/T]TTGAACATAACCAGA | 7347 |
rs575218446 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603285 | AACTGAGTTTATTAG[C/T]TCTTTAGTCTCATGA | 7347 |
rs575243293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75595957 | CTTCTCGAGTTTTAA[A/G]AAAGCCAAATAAACA | 7347 |
rs575260083 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559242 | AGACGGGGTTTCACC[A/G]TATTAGCCAGGATGG | 7347 |
rs575282985 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576919 | GGCCCGCTGTAATGG[G/T]GGGTTCCTTACTTGT | 7347 |
rs575365075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586324 | AAGACATAGCATACA[C/T]GTAACAGAAAGTATG | 7347 |
rs575385099 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549540 | GAGTCCAAGCGTGAG[A/G]GGAGAGGGCTGTGGA | 7347 |
rs575478641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75564911 | ATGTTAGCCTGGCTG[C/G]TCTTGAACTCCTGAC | 7347 |
rs575560935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75580721 | AGTGCTGTATCTACC[C/G]TAGTTTGATCCTCTC | 7347 |
rs575631439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581268 | GGCTGTAAACCAAAA[C/T]CCACTTACTTTATTT | 7347 |
rs575681741 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558302 | TCACTACAGTGGCTG[A/C]GTTTGGTTCCTAGTA | 7347 |
rs575763395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591723 | TATATGACCTACAGC[A/G]TGTTACTTAATGCTT | 7347 |
rs575821961 | in-del | -/TTGA | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75558176 | TATCTCATTTAATTG[-/TTGA]TATGAGTAAGAAGTT | 7347 |
rs575841265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75557213 | GGAGCAAGACCCTGT[C/T]TGAAAAAAAAAAAGG | 7347 |
rs575881056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569073 | GAGCTGCAGAGGAGC[A/T]TGGAACCTGGAGAAA | 7347 |
rs575985337 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555319 | TTGTTTTATTTTCTT[C/T]ACAGTACTTCCCACT | 7347 |
rs576080292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75584544 | GCAGAAGATGAGACA[C/T]GCCCATTTTTAGGCA | 7347 |
rs576087905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583921 | AGAGCTCATATCCAC[C/T]CTCTGCAGACCTCAA | 7347 |
rs576110769 | in-del | -/ATCT | 0.00199481 | 0.0315187 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560179 | AATTCATGGCTATCA[-/ATCT]ATCTATCTTTAAACC | 7347 |
rs576113877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553532 | TTTCCTAATTGCTTC[A/G]AAGAGTCTCTGTTGC | 7347 |
rs576138260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547068 | CTGTAAGTGAAAACC[C/T]GAACAAACCTTATCT | 7347 |
rs576177496 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596260 | AAAATGTGCAACCCT[C/G/T]AGCGTTGTCTACAAT | 7347 |
rs576198997 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576012 | CTACCTCGGCCTCCC[A/G]AAGTGCTGGCATTAC | 7347 |
rs576310473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554222 | TTGCACCATCACACC[C/T]GGCTAATTTTTGTAT | 7347 |
rs576330250 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557974 | TGATTTTTTTTTTTT[-/TT]GAAGACGTGAGTGGT | 7347 |
rs576343038 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UCHL3 | GRCh38.p7 | 13:75555551 | CATTATCTTTAATGC[A/G]GTCATGAATCCTTTG | 7347 |
rs576450959 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572210 | TTCTTCTATCCATTC[A/T]TCAAGACTCAGCTTA | 7347 |
rs576478640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556120 | GAGTACAGTGGGCTA[C/T]TACATTATCTTAAAT | 7347 |
rs576549995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75562764 | GAGCTAAAAACTTGT[C/G]CCTGTTGAAAGGAAG | 7347 |
rs576617822 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569934 | AATAAATTTGTTTCA[C/G]GGTAATGTAATGATC | 7347 |
rs576620296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554867 | CCAGGTACTAAACCT[A/G]GTACCTAATAGTTAT | 7347 |
rs576644138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600246 | GCATATGCTGATGGA[A/G]AAGCTGCAAGTTATC | 7347 |
rs576678426 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75570246 | AACCACACTTTTTTT[G/T]GTTTTTTTTGAGACA | 7347 |
rs576724163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75591797 | TACGTACCTTATTGG[G/T]TTTATACAGGTTGAG | 7347 |
rs576728775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577030 | CAAGAAGGGAGGATC[A/G]CTTGAGGCCAGGAGT | 7347 |
rs576761811 | in-del | -/TTTATGTATGTATGTA | 0.0748549 | 0.178393 | intron-variant | UCHL3 | GRCh38.p7 | 13:75563126 | GGTACCTCATTATCC[-/TTTATGTATGTATGTA]TGTATGTATGTATGT | 7347 |
rs576792413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75561962 | TATAATAGATTTTGA[A/G]GCTATATCCTTCTGA | 7347 |
rs576793274 | in-del | -/CTGT | 0.00465268 | 0.0480072 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590173 | TTCCAGTGACAAGGG[-/CTGT]CTTTTTTTTTTTTTT | 7347 |
rs576849991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75577883 | TTTGTCCATATTAAT[C/T]GAGGAGCCAGCCCAG | 7347 |
rs576952272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547233 | GAGCATTAAATAGAC[A/C]ATCAAGAGGACTCTC | 7347 |
rs576992130 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606244 | AAAATGTGATAGTCA[C/T]GGAGCTTATGTTATT | 7347 |
rs577034096 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596352 | ATAATGGACCTCCAG[A/G]ACAGTTTTGAAGATG | 7347 |
rs577038130 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | COMMD6 | GRCh38.p7 | 13:75547416 | AGTAGGCAGGTTCAA[A/T]ATGCAAAACCCATAA | 7347 |
rs577105504 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75599314 | GTTCTCTGAGTTTGC[A/C]TAGCATTTGAAAATA | 7347 |
rs577190956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75600977 | AATAAGTTGGTTCCA[A/G]TCCTCATGGATGACT | 7347 |
rs577254597 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566092 | TAAACAATATAGAAA[C/T]GTAACAATTAGCAAG | 7347 |
rs577299431 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573336 | TGTATTATTATCTCC[A/G]TTGCTGTTTGTATTC | 7347 |
rs577300878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75601440 | CCACCCCAATCTTCA[A/G]CAACCGCCGTCCTGA | 7347 |
rs577305040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75593704 | GTTTATGTTGAATTT[C/T]TTCCGTTCATAATTT | 7347 |
rs577321182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75571801 | ATTAATCTTTTCTGC[C/T]CCTTTCCCATCTCCC | 7347 |
rs577341082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75556270 | TTCAGTGTTTCCTCA[C/T]TATGTACTTTAATAA | 7347 |
rs577341467 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563178 | GTATATATATGTTTA[C/T]GTTTACTTATTTTTT | 7347 |
rs577361843 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574812 | CAAAGATGGTACATT[C/T]ACTTTTCAGCCTACT | 7347 |
rs577387293 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585792 | TTCTTATACTACATA[C/T]GTAGTGGTGTAATAC | 7347 |
rs577415028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75586455 | ACACTCAGAATCAAT[A/G]AAAAGATACAGAACA | 7347 |
rs577425223 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UCHL3 | GRCh38.p7 | 13:75581791 | TTTAAAGAGTAATTT[A/C]TTCATTTTTTGCTGT | 7347 |
rs577509921 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552311 | TTAGAATTTGGAGAA[A/T]GAATAAACCCTAACA | 7347 |
rs577556320 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75552303 | TAACTGACTTAGAAT[C/T]TGGAGAATGAATAAA | 7347 |
rs577595348 | in-del | -/CCTCTC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580549 | ACTCAGCGGTCTTGT[-/CCTCTC]CCTCTCCCTCTCCTC | 7347 |
rs577620383 | snp | C/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597331 | ACCTGTGAACAGCCA[C/G]TACACTTCTGCCTGG | 7347 |
rs577657311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75568060 | AGGCCACATAAACTA[C/G]GCTATATATATAATA | 7347 |
rs577690324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75553233 | TACCTGTTTTCCTTC[G/T]TTGTAAACTTTCCAC | 7347 |
rs577803048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UCHL3 | GRCh38.p7 | 13:75574134 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 7347 |
rs577867979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75565916 | GGACGTGGGCCCAGG[C/T]AGTCAGCTATAGAGC | 7347 |
rs577922077 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569333 | CTAGTACTAAGCTTT[A/T]CTTAAATTTCCTTCA | 7347 |
rs578001833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75576150 | TTATATCCTAGCTTG[G/T]GATAGGAAACAGATT | 7347 |
rs578005139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605503 | ACAGAGGGCAAGACT[A/C]TGTCTCAAAAAACAA | 7347 |
rs578012109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566632 | GCATTTTTTCTTTTA[C/T]AGACTGAGTTTTTTA | 7347 |
rs578214822 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | UCHL3 | GRCh38.p7 | 13:75554628 | TCCTTTTGCTTCCCT[-/A]AAAATCTAATTTCCA | 7347 |
rs578223221 | snp | A/C | 0.000113876 | 0.00754486 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590014 | TGTGTCACCATGCAT[A/C]CCTGCCCTGGGTCAA | 7347 |
rs578245935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UCHL3 | GRCh38.p7 | 13:75583672 | CATTTTCACTAAAGC[A/G]TAATTGTAGAAAACC | 7347 |
rs578246756 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577818 | TTGCCTTCAGACCCT[A/T]CTTTTACTTCATTGC | 7347 |
rs745318079 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564036 | TTGGGTACATTCAGG[A/G]TACTATGGTCATAGA | 7347 |
rs745319631 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579126 | AAATTGAGGTGCTCA[C/T]ATATTTATTTCCCTC | 7347 |
rs745353936 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570012 | TTCCTTCTCTTGCCT[C/T]TTTTTTCATTTTTTG | 7347 |
rs745434848 | snp | A/G | 3.35385e-05 | 0.00409489 | missense | UCHL3 | GRCh38.p7 | 13:75560809 | TGATGTATATGGAAT[A/G]GATCCTGAACTCCTT | 7347 |
rs745490042 | snp | A/G | 3.31818e-05 | 0.00407306 | missense, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604796 | CATTTCCAATTAACC[A/G]TGGTGAAACTAGTGA | 7347 |
rs745524445 | snp | A/G | 1.65844e-05 | 0.00287957 | splice-acceptor-variant, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605727 | TTTTTTTTCCTCCAT[A/G]GGATGCCATAGAAGT | 7347 |
rs745575992 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551604 | TAAATATATAAAAAG[C/T]AACATATGACCAAGA | 7347 |
rs745617435 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587897 | AGTGGTTTCCCCCAG[C/G]TCAGTATTCCTCTCT | 7347 |
rs745792786 | snp | C/T | 1.87499e-05 | 0.0030618 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560909 | TAAAATAGAAAGTTT[C/T]TGGTAAATACAATTT | 7347 |
rs745861537 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559505 | CAAGTAGATTATCTT[C/T]TACAAGCAGAGAAAT | 7347 |
rs745887047 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575304 | GCCCCACCTCACTTA[C/T]GCTTCATTAACTTAC | 7347 |
rs745908532 | in-del | -/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549961 | CTAAAGCGTGTTCTC[-/T]TGTTTCGTTTTCAGG | 7347 |
rs745959457 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591213 | CTGTGAAGTGGTATC[C/T]TTCCTTAAATATTTG | 7347 |
rs746001399 | snp | C/G | 1.68173e-05 | 0.00289972 | intron-variant, upstream-variant-2KB, splice-donor-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549863 | GAGGCCAATCCCGAG[C/G]TGGGCGCGCTTCGGG | 7347 |
rs746037850 | snp | C/T | 1.74637e-05 | 0.00295492 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569555 | ATAAATTTAACCATA[C/T]AAATTTCTTGCTGTA | 7347 |
rs746080201 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603307 | GTCTCATGAATGACA[C/T]ACACACAGAAATGAT | 7347 |
rs746084610 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569264 | GTTTTCAGAGATTTA[C/T]GGGTTACACAGTACA | 7347 |
rs746104640 | snp | A/G | 6.29069e-05 | 0.00560799 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549803 | GCTGTCAGAGCTGGA[A/G]GGCCGGGCACCGCGG | 7347 |
rs746147867 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570971 | AAGGTGTGGATTATT[C/G]TTTTTGACTAAGTTT | 7347 |
rs746180149 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556021 | ATCATACTGGTCACC[C/T]GCCTTTGGGCTTTCT | 7347 |
rs746195304 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605051 | TGAAAAGGCAAGAAT[A/G]GTATTGAAAGACTTG | 7347 |
rs746314174 | snp | C/T | 1.74306e-05 | 0.00295211 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566892 | TTTTCCCCCTTAAGA[C/T]ACAAGTTAATTGCAT | 7347 |
rs746443926 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566366 | GATGTCTTAGACCAA[C/T]CTCCTACAAAGGAAA | 7347 |
rs746455726 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551856 | TTTTTTAATACCAGT[A/G]ATCTGAACAGGAGCT | 7347 |
rs746551857 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553245 | TTCTTTGTAAACTTT[A/C]CACAAAGAATTGTTC | 7347 |
rs746623985 | snp | G/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598852 | CTGGATTATCATTAT[G/T]ACTATTGCCAAATGG | 7347 |
rs746626249 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587984 | TGTGAATTGCCACAA[A/C]CGTATTGATGATCAT | 7347 |
rs746639157 | snp | A/C | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601488 | ACATCAAAGCAAGCC[A/C]CTCCATCAGCAAAAA | 7347 |
rs746736860 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575564 | CAGCCCTATGAGGTA[G/T]TACCATTGTCCTCAT | 7347 |
rs746790097 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591342 | ACGACATTCTTCATT[A/T]TTATTCGTTCATCCA | 7347 |
rs746805420 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561180 | TCAAGTGATCCTCCC[A/G]CATCGGTCTCCCAAA | 7347 |
rs746818372 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576348 | AATTCTCCTGCCTCA[A/G]CCTCTCAAGTAGCTG | 7347 |
rs746890070 | snp | G/T | 2.53431e-05 | 0.00355962 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605711 | CTGAAAAATCATACT[G/T]TTTTTTTTCCTCCAT | 7347 |
rs746898203 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550032 | CGGAGTCTTTTCTGT[C/T]TGCTCGGTCCGCTTC | 7347 |
rs746951082 | snp | A/G | 1.66671e-05 | 0.00288674 | utr-variant-5-prime, missense | UCHL3 | GRCh38.p7 | 13:75560792 | CCTAACTGGCAATTC[A/G]TTGATGTATATGGAA | 7347 |
rs746979884 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561983 | ATCCTTCTGATTTTT[A/G]TTTTTAAAATTAGAA | 7347 |
rs747021143 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571296 | GAGTTTCATCCAAAT[C/T]ATGGATTTACATTTA | 7347 |
rs747043840 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559032 | TCAGCCCCGGACTCT[-/TT]TTTTTTTTTTTTTTT | 7347 |
rs747070077 | snp | C/T | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605378 | CTGGGTGTGGTGGTA[C/T]GTGACTGTAGTCCCA | 7347 |
rs747111272 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572618 | CAACATATGTGTATT[A/G]ATTAACCAGAATTAG | 7347 |
rs747161304 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75567309 | ATACCTGGAGAACTA[C/T]GATGTCGGTACCTTC | 7347 |
rs747191747 | in-del | -/T | 0.0225677 | 0.1038 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560724 | ACTAATGTTCCATTG[-/T]TTTTTTTTTTCTTTC | 7347 |
rs747271184 | snp | A/G/T | 3.30187e-05 | 0.00406306 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569441 | TTTTTTCCAATGAAT[A/G/T]CCTTTATTCTTATTA | 7347 |
rs747341559 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593648 | ACCTGTGGAATTCTG[A/T]AGTTCTAGAGTGAAG | 7347 |
rs747413832 | snp | C/T | 4.0286e-05 | 0.00448792 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566661 | TAATATGTTATTTTC[C/T]ACAAATACACTGTTG | 7347 |
rs747475769 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580546 | TAGACTCAGCGGTCT[C/T]GTCCTCTCCCTCTCC | 7347 |
rs747479433 | in-del | -/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596341 | TTGGTAGTATATAAT[-/G]GGACCTCCAGGACAG | 7347 |
rs747533238 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581018 | TTTGTTCTTTTTTGC[C/T]GTTAACATCTAAGTC | 7347 |
rs747567254 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587578 | TCAGGAAAAAAAGTT[-/A]ATGTAGAAAAAGGAA | 7347 |
rs747574140 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589078 | TGTCCCATGTTAGCA[C/T]TAACATATTTTTCTT | 7347 |
rs747594762 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554703 | GACTTCCTGCTTATC[A/G]TACTCTACTGGTCTT | 7347 |
rs747615850 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565192 | TTTCCTACACATTAC[A/C]TCTTGAAATTATCAA | 7347 |
rs747751143 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | UCHL3 | GRCh38.p7 | 13:75566795 | CAATCAGCAATGCCT[A/G]TGGAACAATTGGACT | 7347 |
rs747785087 | in-del | -/TTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559031 | CTCAGCCCCGGACTC[-/TTT]TTTTTTTTTTTTTTT | 7347 |
rs747974688 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599134 | CACCATGCCTGGCTA[-/T]TTTTTTTTTTTTTTT | 7347 |
rs747999391 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591776 | GTAAGATGGGTATAA[C/T]TATATTACGTACCTT | 7347 |
rs748110353 | snp | C/T | 1.67804e-05 | 0.00289653 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604723 | TTGAAAGCACATTAT[C/T]CTGTAAAAACAGCTA | 7347 |
rs748131273 | snp | A/C | 1.66123e-05 | 0.00288199 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549880 | GGGCGCGCTTCGGGG[A/C]AGCCCTGGGCCGTGG | 7347 |
rs748145806 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584784 | AAGAATCAAATGGAA[A/G]TGCCAGTAATGAAAA | 7347 |
rs748168216 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573940 | GTCACTTTTCAGGCT[A/G]GGCGCGGTGGCTCAC | 7347 |
rs748178267 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598663 | AACTGCAGAAATAAT[A/G]CTGCGTTCTTCTCAG | 7347 |
rs748213141 | snp | A/T | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606447 | CTGTCATAAAGGTGG[A/T]GGGGAAGAGCAGAAG | 7347 |
rs748249228 | in-del | -/AAT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574337 | CACTTTAAAATAGTC[-/AAT]AATAAGTTTTTTCTT | 7347 |
rs748304370 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | UCHL3 | GRCh38.p7 | 13:75567275 | AATCTGTGTCAATGA[A/G]CCCTGAAGAACGAGC | 7347 |
rs748337069 | in-del | -/CTGAAC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565292 | TAAGACCTTAACATA[-/CTGAAC]CTTTCCAGTTTTTTA | 7347 |
rs748353238 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593862 | CTTCATATTACAACT[A/G]CTTGAAAATATATAC | 7347 |
rs748441164 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594876 | CTGATTTGTTTGACT[A/G]CTAATGTATATAATA | 7347 |
rs748455544 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581409 | GGCGGCAGTGCAGTG[A/G]GTCGATCTTGGCTCC | 7347 |
rs748504423 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596916 | CAAAGGCAGAACTAC[G/T]GAGGTCTTGTTTGGT | 7347 |
rs748605945 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552522 | TGCAGATGAGTATTA[A/G]TTGTTAGACATTAGC | 7347 |
rs748607991 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586685 | GAATGTTTTCTATTC[A/G]TAGTGGAGTTAAACT | 7347 |
rs748641125 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568336 | GCATTCCAATATACT[C/T]TGAGAATTTTAAATT | 7347 |
rs748671093 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601670 | AGGAAACAAAAAAAT[G/T]TGTGACTCATTTTAT | 7347 |
rs748678040 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576502 | TGGGACTACAGGCGC[A/G]TGCCACCACACCCAG | 7347 |
rs748725964 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553579 | CAACTTCTAAGGAGC[A/G]CCTCAGCCACTTCAT | 7347 |
rs748755293 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591923 | CATTTAAAATCCACA[A/G]TGCTGCAGTTAGCAT | 7347 |
rs748813884 | in-del | -/AAC | | | intron-variant, cds-indel | UCHL3 | GRCh38.p7 | 13:75597541 | TTTTGAAAACAACAT[-/AAC]AACTATTTACATAGC | 7347 |
rs748891906 | snp | A/G | 1.65397e-05 | 0.00287569 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605826 | AGCTTGTCAATAATG[A/G]AAACACCAAAAACTG | 7347 |
rs748896792 | snp | A/T | 3.44252e-05 | 0.00414866 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566646 | ACAGACTGAGTTTTT[A/T]AATATGTTATTTTCC | 7347 |
rs748918344 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577647 | ACTAAAGTGTCTAGT[A/G]GATTAGAAGATCTCC | 7347 |
rs748985284 | snp | A/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597751 | AGAGATGACTGTAAC[A/T]TTATTTTTAAAAATA | 7347 |
rs748991248 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573268 | AGACTCTGTCTCAGA[-/A]AAAAAAAAAAAAAAA | 7347 |
rs748996737 | snp | A/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598779 | GTTAAGAAGTATGTC[A/T]TGCAGTTGCTCATCA | 7347 |
rs749038412 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563648 | TAAAATCTTATTTAA[C/T]AAAAATTTCTAATGC | 7347 |
rs749102220 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594885 | TTGACTACTAATGTA[C/T]ATAATACCTATTTTT | 7347 |
rs749159467 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586413 | AAAGAGAAATAGACA[A/G]ATTCACAATTATAGT | 7347 |
rs749179283 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565976 | TATTGCTTTTACAAC[C/G]AGTTATTATAGATAA | 7347 |
rs749259810 | snp | A/G | 0.000166099 | 0.00911164 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589890 | TAAGAATAAATGATC[A/G]CCCAGTAACGTGGTC | 7347 |
rs749268109 | in-del | -/AC | 5.50282e-05 | 0.0052451 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566668 | TTATTTTCCACAAAT[-/AC]ACTGTTGACTTTTTT | 7347 |
rs749335622 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560962 | TTGAGGCAGTATCTC[C/G]CTCTGTTGCCTAGGC | 7347 |
rs749370546 | in-del | -/AC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592435 | TATATATATATATAT[-/AC]ATATATATATATATA | 7347 |
rs749414290 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572447 | TTATTCCCATCTTAG[-/T]GGTTCACAAAATGGT | 7347 |
rs749489510 | snp | A/C | 1.6766e-05 | 0.00289529 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549868 | CAATCCCGAGGTGGG[A/C]GCGCTTCGGGGCAGC | 7347 |
rs749531344 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583044 | TTGTATAGTGCGTTC[A/G]TTTAGCATGAGGAGG | 7347 |
rs749563345 | in-del | -/CA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575868 | GCGATTCCCCTGCCT[-/CA]GCCTCCCAAGTAGCT | 7347 |
rs749599401 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568679 | ATAGTTTTTCTTCTT[G/T]TTCACTATTTTAATA | 7347 |
rs749653535 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569982 | GTTAGCTAGTTCAGC[-/T]GGGTTGCTTTTCCTT | 7347 |
rs749694280 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570939 | ATATATATTGGTTGC[C/T]CTAGGCGCTGCTTTC | 7347 |
rs749696191 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554859 | TTCATCACCCAGGTA[C/G]TAAACCTAGTACCTA | 7347 |
rs749754487 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557859 | ACCCAAGCTAACTGC[C/T]AACATTTTAGAAAAT | 7347 |
rs749761672 | snp | A/G | 1.75142e-05 | 0.00295919 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566901 | TTAAGATACAAGTTA[A/G]TTGCATTGAGCAGTA | 7347 |
rs749765284 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603055 | AGTGCAGTGGCATGA[C/T]CATAGCTTGCTGCGT | 7347 |
rs749816740 | snp | A/G/T | 3.29779e-05 | 0.00406055 | missense | UCHL3 | GRCh38.p7 | 13:75567265 | TTCCTGGAGGAATCT[A/G/T]TGTCAATGAGCCCTG | 7347 |
rs749852276 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590681 | TGGCTCAGGTACTTG[A/G]TTTAATCTTGATCTG | 7347 |
rs749893054 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559911 | TGAAAATGACATTCT[C/T]ATTTTTTCTCTATGT | 7347 |
rs749913833 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549413 | CGCGGCACGCCTCCT[A/G]GCGCAGTCGGTTGAC | 7347 |
rs749920687 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595455 | ATGCAAAATTAGCCC[A/G]GCGTGGTGGCACATG | 7347 |
rs749934725 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557029 | CAGACCAGCTTGGGC[A/C]ACATAGTGAGACGTC | 7347 |
rs749940187 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560222 | TTTGGTAAATAGGAT[A/G]AACTATGTTGATTTT | 7347 |
rs749961254 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580419 | GTGTTCTCATGCATG[C/T]GCACACACATGTCCT | 7347 |
rs750019599 | snp | A/T | 1.65318e-05 | 0.002875 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605822 | GCATAGCTTGTCAAT[A/T]ATGGAAACACCAAAA | 7347 |
rs750068505 | snp | A/G | 1.65127e-05 | 0.00287334 | missense | UCHL3 | GRCh38.p7 | 13:75569467 | TATTACAGGCCATCC[A/G]AGTTACTCATGAGAC | 7347 |
rs750111627 | snp | A/G | 5.2404e-05 | 0.00511852 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549778 | AGCGGCGGCGGCGGC[A/G]AAGGCGGCGGCTGTC | 7347 |
rs750112575 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582203 | AGTGAATGTGTGTGT[A/G]TGTTTAAACTCAGAG | 7347 |
rs750118902 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566303 | TCTATTATGCTTTAT[A/G]GTATTCTATTACGAT | 7347 |
rs750145683 | in-del | -/TTCC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572033 | GTCTTGTCTTTACTT[-/TTCC]TTCCTTCCTTCCTTC | 7347 |
rs750175027 | snp | A/C | 1.7174e-05 | 0.00293031 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566874 | ATTTTTCATTACTGC[A/C]TTTTTTCCCCCTTAA | 7347 |
rs750192107 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603623 | CATAATGAATGTGAT[A/G]GTCATATAAACATAG | 7347 |
rs750275759 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555147 | TCTGTTCCTGCTTCA[C/G]AGTCTTTGCACTTGC | 7347 |
rs750326610 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75601074 | AATTAGAAGGGGAGC[A/C]TGAAGATGTGACTGA | 7347 |
rs750473410 | snp | C/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549871 | TCCCGAGGTGGGCGC[C/G]CTTCGGGGCAGCCCT | 7347 |
rs750513889 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562966 | CCCTATTTCAGCTTA[C/T]AGGTGATATATTGCA | 7347 |
rs750526360 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592833 | TTGAGTCACTACATT[G/T]GGTAATTGCTTACAT | 7347 |
rs750557779 | snp | A/G | 0.000115503 | 0.00759856 | missense | UCHL3 | GRCh38.p7 | 13:75594966 | ATTGCATTAGTTCAT[A/G]TAGATGGGCATCTCT | 7347 |
rs750596431 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579554 | GTCTGTCTTCCCTTC[-/T]TTTTTTCCTCTCCAT | 7347 |
rs750605453 | snp | G/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550841 | CAATTCACCGTGTTC[G/T]TAAAAATATTGGTTT | 7347 |
rs750645171 | snp | G/T | 0.00217352 | 0.0328943 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590175 | CCAGTGACAAGGGCT[G/T]TCTTTTTTTTTTTTT | 7347 |
rs750684123 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547935 | TATGGAAAGCTACCA[A/G]TTTGAGTGTATCCCT | 7347 |
rs750745796 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572348 | TCATATTCTCTTTCA[C/T]TTTTTAAGATGTACT | 7347 |
rs750779334 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573765 | TTTTCAAATATAGTC[A/G]CGTTGAAGGTTAGGG | 7347 |
rs750860734 | snp | C/G | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606045 | ACTAGCAATAGCTTT[C/G]TTATTCTTTTTAGAT | 7347 |
rs750898465 | snp | C/G | 1.64727e-05 | 0.00286986 | splice-acceptor-variant, upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549975 | TCTGTTTCGTTTTCA[C/G]GTCACCAACCAGGTG | 7347 |
rs750915224 | in-del | -/ATA | 3.41565e-05 | 0.00413244 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569540 | TAAATTTTTCTTGCT[-/ATA]AATTTAACCATATAA | 7347 |
rs750950034 | snp | C/T | 0.000209881 | 0.0102419 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560735 | CATTGTTTTTTTTTT[C/T]TTTCTTTCTTTTACC | 7347 |
rs750968244 | in-del | -/T | 0.020951 | 0.100183 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605709 | ACTGAAAAATCATAC[-/T]TTTTTTTTTTCCTCC | 7347 |
rs751021338 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582693 | TGTGAAAAATTAGCC[A/G]TCTAGCTCAAGATTC | 7347 |
rs751039964 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557803 | TTGTAAAACTAATGC[-/T]TTTTATAAAATACTA | 7347 |
rs751046842 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548551 | GCTCATCAAAGGCAT[C/T]ATCCCTTAAAACAGA | 7347 |
rs751063848 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583915 | GAAGGGAGAGCTCAT[A/T]TCCACTCTCTGCAGA | 7347 |
rs751108156 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568245 | TTAGGCGTATAATCT[A/G]CAAATTATTTGGTTA | 7347 |
rs751145532 | snp | A/G | 4.95176e-05 | 0.00497558 | missense | UCHL3 | GRCh38.p7 | 13:75567248 | GATCAACCTTGAAAA[A/G]ATTCCTGGAGGAATC | 7347 |
rs751231268 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602682 | GAAGGACCAAGTAGT[A/G]AATATTTTAGGTTTT | 7347 |
rs751253240 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567358 | GTGGGCAAAAGTTTG[C/T]GGGATTGTAGATGTG | 7347 |
rs751258785 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560550 | TGAACATATTTAGAG[C/T]GTGCATTGTGATGTT | 7347 |
rs751261170 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554581 | CCTTAGCTTGGACAA[C/G]TATAGTAGGCTCCTA | 7347 |
rs751298578 | snp | A/C | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550510 | TCTTCCAGTCTTTTA[A/C]AGCTGGACATTTAGT | 7347 |
rs751350896 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555289 | AGCCCCCCAAATCTG[C/T]ACTGTCATCCTCACT | 7347 |
rs751369997 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582089 | ACTCACTAGTTATGT[-/G]GCTTTGGGCAAGTCA | 7347 |
rs751407270 | in-del | -/AA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573267 | GAGACTCTGTCTCAG[-/AA]AAAAAAAAAAAAAAA | 7347 |
rs751454652 | snp | C/T | 3.69884e-05 | 0.00430033 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560899 | AATTGTTATGTAAAA[C/T]AGAAAGTTTCTGGTA | 7347 |
rs751489502 | snp | A/G | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606274 | TGTGAGAAGAGATAA[A/G]TAACAAACACATCAA | 7347 |
rs751527787 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599818 | ATTCAAGTCACACGT[C/T]TCTCACTTTAAGTCA | 7347 |
rs751552546 | snp | C/G | 1.65072e-05 | 0.00287286 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605798 | TTTAATGCGATTGCT[C/G]TTTCTGCAGCATAGC | 7347 |
rs751584091 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577029 | CCAAGAAGGGAGGAT[C/T]GCTTGAGGCCAGGAG | 7347 |
rs751662321 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587551 | TGATATATGTAACTT[A/G]TCTTCAAATGATTCA | 7347 |
rs751679897 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568302 | CCTGATAAATTAATT[A/G]GTTTGATTATGTTGT | 7347 |
rs751682296 | snp | A/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551029 | TTCCCCCTAGTTTGC[A/T]GAGAGTTTTTCTTAT | 7347 |
rs751683064 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600793 | CTTTCATTTCTTGTT[A/G]TTTAAGAAATACAGT | 7347 |
rs751696432 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552726 | TATGCATTTAAAGGG[A/G]TAAATGCAGCTTGCA | 7347 |
rs751810421 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549954 | GTTTGTCTCTAAAGC[A/G]TGTTCTCTGTTTCGT | 7347 |
rs751817651 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573805 | ATGAATTTGGCAGGG[A/G]GGACACAATTCAGTC | 7347 |
rs751872412 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560623 | ACATTTGTATTTTAT[A/C]CCTTTATAGGTATTA | 7347 |
rs751905614 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575055 | TAGCTTCATCACTGG[C/T]ATCACTGGTACTCTC | 7347 |
rs751919919 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586483 | ACATTACTAAAAAAT[C/T]GAAGATTTGAACAAC | 7347 |
rs751959813 | snp | A/C | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547373 | ACTTTGTGAGTATAG[A/C]TTTGGGAATTACCAA | 7347 |
rs752087544 | snp | A/G | 9.10539e-05 | 0.00674675 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590089 | GTCTTCGTCGCTGGC[A/G]ACCCTTCTTACGTCT | 7347 |
rs752094546 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594723 | CACTGTTTTCTTTGC[C/T]GATAACTGAGCACAT | 7347 |
rs752265273 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589412 | ACCTGTCAGCCTAAG[-/T]AGGAGGATAGTTTAT | 7347 |
rs752285525 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555451 | CGGTGCCAGGCTCAC[A/G]GGGCCATCAACAAAT | 7347 |
rs752342447 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556992 | GAGGCCGGGGCCAGA[C/G]GATTGCTTGAGTGTA | 7347 |
rs752351086 | snp | G/T | | | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604619 | TAAAAAATATTCATG[G/T]TAGCACATTAAAACA | 7347 |
rs752353709 | snp | C/G/T | 3.46911e-05 | 0.00416468 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566885 | CTGCATTTTTTCCCC[C/G/T]TTAAGATACAAGTTA | 7347 |
rs752360784 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591482 | AGCACAATTGATCCA[A/G]TTCTAATGTGAATTA | 7347 |
rs752414958 | snp | A/C/G | 9.92474e-05 | 0.00704371 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605747 | GCCATAGAAGTTTGC[A/C/G]AGAAGTTTATGGAGC | 7347 |
rs752453844 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595816 | AAGTTTACCTTTCAG[C/T]GGACTATTTCATGGC | 7347 |
rs752550414 | in-del | -/TGTCTTGTCT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571986 | AACCCTGTCTTGTCT[-/TGTCTTGTCT]TGTCTTGTCTTGTCT | 7347 |
rs752568540 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553357 | GTAGTAACTTTTTTT[-/G]TCAAGTTCACTAATG | 7347 |
rs752656754 | in-del | -/GTTTAAT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591027 | TATCTTAAAGCTTTG[-/GTTTAAT]GTGTGTGCCATACAT | 7347 |
rs752730019 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564644 | CTTTTCTCCACACCC[G/T]CACCATTATTTATTA | 7347 |
rs752742777 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575279 | AGCTAATACAGAAAT[C/G]TGAACAGTAGCCCCA | 7347 |
rs752746274 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584369 | AGTGGAACAAGAGCA[-/T]TGAAAAAGAAAACAT | 7347 |
rs752787799 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588494 | AGACATTATCATATA[C/T]ACTTTTGTTCCCATA | 7347 |
rs752843344 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589354 | ATATTTAATGATATT[A/G]TTTCCTAAAAGATAG | 7347 |
rs752864495 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597706 | ATGAGATGGGGCCGG[C/T]GTCCTGGAACCAGTC | 7347 |
rs752943510 | snp | C/T | 0.00010015 | 0.00707567 | utr-variant-5-prime, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560782 | AGGTCTACATCCTAA[C/T]TGGCAATTCGTTGAT | 7347 |
rs752958414 | snp | C/T | 1.66657e-05 | 0.00288662 | utr-variant-5-prime, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560797 | CTGGCAATTCGTTGA[C/T]GTATATGGAATGGAT | 7347 |
rs753012912 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588615 | CATCAAAATGATAGC[-/T]TTTTTTTAAAGGTTA | 7347 |
rs753044785 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595935 | TTCTTATTCTTTTCC[A/G]TAAGACCTTCTCGAG | 7347 |
rs753063819 | snp | C/T | 8.85857e-05 | 0.0066547 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590067 | AAGGCTACCAGTCCA[C/T]CTCTCCGTCTTCGTC | 7347 |
rs753133025 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582878 | TCCATAATAGCACAC[C/T]TTATTTCAAAGTCCT | 7347 |
rs753254220 | snp | C/T | 1.68815e-05 | 0.00290525 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569524 | TATTTCACATTTTTT[C/T]TAAATTTTTCTTGCT | 7347 |
rs753348223 | snp | A/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605947 | AACTTTGCCTTAACC[A/T]GTGTTTTATGTTATT | 7347 |
rs753389756 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573537 | GGCTTCTACTGAGAT[A/G]TCCCTTCCTGGCTTG | 7347 |
rs753456567 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | UCHL3 | GRCh38.p7 | 13:75566753 | AGGGACAAGATGTTA[C/T]ATCATCAGTATATTT | 7347 |
rs753514395 | snp | A/G | 1.8329e-05 | 0.00302723 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549827 | ACCGCGGCCATGGAG[A/G]GTCAACGCTGGCTGC | 7347 |
rs753553438 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594397 | AATGCTTATTTTACT[C/T]AAAGACTGTTTACAC | 7347 |
rs753556228 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579095 | CATTCCAATAAGCCA[A/G]AAATGATTTACGCAC | 7347 |
rs753607381 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599136 | CCATGCCTGGCTATT[-/T]TTTTTTTTTTTTTTT | 7347 |
rs753624100 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572474 | TGGTGTGTCATGGAA[C/T]CAATGGCGCCTTAGT | 7347 |
rs753625848 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600635 | GCTCAGAAAAAGATT[A/C]CTTTGAAAATATTAC | 7347 |
rs753699858 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565960 | GCTTATTATTATACC[C/T]TATTGCTTTTACAAC | 7347 |
rs753793107 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600179 | TAGCAGTTGGTTCAT[C/G]AGGTTTAAGGAAAGA | 7347 |
rs753804961 | snp | A/G | 6.62921e-05 | 0.00575688 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567217 | ATTTTATCTTCTTTC[A/G]TATTCTCAGAATCTG | 7347 |
rs753805839 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576294 | GAGTGTAGTGGCGCA[A/G]TCTCTGCTCACTGCA | 7347 |
rs753858266 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556478 | AACAGGGCAGAATCT[C/T]TGGCTGCCCTGAACA | 7347 |
rs753866681 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552939 | TTTATATGGACCCCT[C/T]TCCACCCCAAGGATT | 7347 |
rs753965442 | in-del | -/CTAT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593919 | TTTTTATTTAAGATA[-/CTAT]CTGTTACTGAAAGGA | 7347 |
rs753978810 | snp | C/T | 0.000111763 | 0.00747456 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560743 | TTTTTTTCTTTCTTT[C/T]TTTTACCAGTTTCTT | 7347 |
rs753987595 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576909 | GTATACAGTTGGCCC[A/G]CTGTAATGGTGGGTT | 7347 |
rs754011321 | snp | A/T | 5.17531e-05 | 0.00508664 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605691 | GTAAGTAAAACACTT[A/T]TACACTGAAAAATCA | 7347 |
rs754068075 | snp | C/T | 3.34163e-05 | 0.00408742 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595011 | AACTATTTTAATTTG[C/T]CCTGGGGAGAGAAAT | 7347 |
rs754080767 | snp | G/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598474 | TCCAGGATTATGTGT[G/T]GAATTTGTCATGTTT | 7347 |
rs754089714 | snp | A/G | 3.29451e-05 | 0.00405851 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549997 | AACCAGGTGAGTGAG[A/G]TGTCTGTCGCTCGGG | 7347 |
rs754110303 | snp | C/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548978 | TCACAGCACCTTCCT[C/G]TCTGCCTAGGTAAAG | 7347 |
rs754147510 | snp | A/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596882 | TTTAAAATTGGTTTG[A/T]AGTAAGAACTTCATA | 7347 |
rs754156467 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561448 | TTTAATAAAAATTTG[A/G]TTAGTTTGCCTCAGC | 7347 |
rs754323498 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549641 | AAATATGACACTTGA[-/C]CTACGGCCCTGCACG | 7347 |
rs754439043 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572166 | AGTACTCTCTTTCTG[A/G]AAATATTCTTTCCCT | 7347 |
rs754453843 | snp | A/G | 1.6492e-05 | 0.00287154 | missense | UCHL3 | GRCh38.p7 | 13:75566785 | ATGAAGCAAACAATC[A/G]GCAATGCCTGTGGAA | 7347 |
rs754510127 | snp | A/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601637 | CAGAGTAATATAAAC[A/T]TAACTTTTATATGCA | 7347 |
rs754578079 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576990 | CATGGTAGCTCATGC[C/T]AGTAATGCCAGCACT | 7347 |
rs754598205 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550260 | TTGGAGGGACTTTTA[-/C]CCTGTATTCCTATTC | 7347 |
rs754694907 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589850 | GTAGACCATATGAAT[A/T]ACAAGCATGACCATA | 7347 |
rs754761153 | snp | A/C | 1.67911e-05 | 0.00289746 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595024 | TGTCCTGGGGAGAGA[A/C]ATGGTAAATGGGAAA | 7347 |
rs754865993 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576377 | TGGGACTACAGGCAC[G/T]TGCCACCACACCCGG | 7347 |
rs754927677 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597245 | TTCCTGTAGTCCCAC[G/T]TTCTGTAGTGGGAAG | 7347 |
rs754959107 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562004 | AAAATTAGAAACAGT[A/G]GGATGATTGCAGTAG | 7347 |
rs754993909 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579182 | TCATTTTGAAAGAAT[C/G]TGAGGATATTAGGAA | 7347 |
rs755082504 | snp | C/T | 1.80517e-05 | 0.00300425 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560746 | TTTTCTTTCTTTCTT[C/T]TACCAGTTTCTTAAA | 7347 |
rs755099536 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550005 | GAGTGAGGTGTCTGT[C/T]GCTCGGGACCTCGGA | 7347 |
rs755101030 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587612 | AGTATAAGTGCAGAT[A/G]ATAAAGCAAATGGAA | 7347 |
rs755171976 | snp | C/T | 1.71434e-05 | 0.0029277 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605697 | AAAACACTTTTACAC[C/T]GAAAAATCATACTTT | 7347 |
rs755264078 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593340 | ATTAGACTGAGGTGG[C/T]CAGTAATATTTTTTG | 7347 |
rs755293457 | snp | G/T | | | utr-variant-5-prime, missense | UCHL3 | GRCh38.p7 | 13:75560755 | TTTCTTTTACCAGTT[G/T]CTTAAACAATTAGGT | 7347 |
rs755390303 | snp | C/G | 1.65214e-05 | 0.0028741 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569433 | TATAGGCATTTTTTC[C/G]AATGAATACCTTTAT | 7347 |
rs755484954 | snp | A/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547384 | ATAGATTTGGGAATT[A/G]CCAATAAATTTTAGC | 7347 |
rs755494947 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581226 | TTTCATAATAATAGT[A/G]TGTCCATTTAAATGA | 7347 |
rs755498430 | snp | C/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548616 | GTTTTAATTTTTTCA[C/G]CATTTATTTCTCACA | 7347 |
rs755531559 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555527 | TTCCTGCTCCAGAAG[A/T]TCTCCCAACATTATC | 7347 |
rs755549913 | snp | A/G/T | 3.30667e-05 | 0.00406602 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605823 | CATAGCTTGTCAATA[A/G/T]TGGAAACACCAAAAA | 7347 |
rs755600800 | snp | A/G | 1.89744e-05 | 0.00308007 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560920 | GTTTCTGGTAAATAC[A/G]ATTTTTGTTTTATTC | 7347 |
rs755662771 | snp | C/T | | | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604680 | TTTTAACTTTTCTTG[C/T]CTCACTGGGGGAAGA | 7347 |
rs755761440 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557042 | GCAACATAGTGAGAC[A/G]TCTCTACTAAAAAAT | 7347 |
rs755762408 | snp | G/T | 2.95225e-05 | 0.00384192 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549784 | GGCGGCGGCGAAGGC[G/T]GCGGCTGTCAGAGCT | 7347 |
rs755795882 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577429 | ATACAGGAGGAGGTA[C/T]ATAGGTTATATGCAA | 7347 |
rs755887167 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563307 | CAGTCTCTGGAGTAG[C/G]TGGGATTTCAGGCGT | 7347 |
rs755950529 | snp | C/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598684 | TTCTTCTCAGTGCAT[C/T]ATATCGAGAGGCACA | 7347 |
rs756003345 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564649 | CTCCACACCCTCACC[A/T]TTATTTATTATCTCT | 7347 |
rs756013143 | snp | A/G | 3.3123e-05 | 0.00406945 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75566742 | AATAAAATCTCAGGG[A/G]CAAGATGTTACATCA | 7347 |
rs756108017 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600154 | AAGCTACAGAAGAAA[G/T]GTCTGAAGCTAGCAG | 7347 |
rs756178407 | snp | G/T | 1.681e-05 | 0.00289909 | intron-variant, upstream-variant-2KB, splice-donor-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549864 | AGGCCAATCCCGAGG[G/T]GGGCGCGCTTCGGGG | 7347 |
rs756180319 | snp | A/G | 3.30393e-05 | 0.0040643 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75594974 | AGTTCATGTAGATGG[A/G]CATCTCTATGAATTA | 7347 |
rs756229991 | in-del | -/AG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584940 | AAAAAATAGTGGAAA[-/AG]AGGGGGAAAAACCAC | 7347 |
rs756232946 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571827 | CTCCCACAGTTTAGA[A/C]ACACTACTGGAGTGA | 7347 |
rs756268349 | snp | G/T | 1.64988e-05 | 0.00287213 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594871 | CATGACTGATTTGTT[G/T]GACTACTAATGTATA | 7347 |
rs756317737 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575317 | ATGCTTCATTAACTT[-/A]ACACTGAAAGGTATT | 7347 |
rs756322856 | snp | A/C | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75595998 | GAAGTTCTTTTCAGT[A/C]ATTCTAGATACCGTG | 7347 |
rs756325539 | snp | C/T | 1.6834e-05 | 0.00290116 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560815 | ATATGGAATGGATCC[C/T]GAACTCCTTAGCATG | 7347 |
rs756346044 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547535 | GATGCCCAATCTTGG[A/G]CTCTGTCTCAGACTT | 7347 |
rs756386031 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568821 | TAAAATAGTTTGCAT[A/G]TTTTTAAGGCTTGGA | 7347 |
rs756434004 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548739 | CACTGGGTTAGGCCC[C/T]GGATAAATAATGTGA | 7347 |
rs756472159 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590936 | CAGAATTAAGCAACT[A/G]CAGCTCTTGTCTTTC | 7347 |
rs756509579 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557604 | TGGGATGCTTCTAAT[G/T]AACTGTGTAGAGATG | 7347 |
rs756520815 | snp | C/G | 3.3006e-05 | 0.00406226 | missense | UCHL3 | GRCh38.p7 | 13:75567252 | AACCTTGAAAAAATT[C/G]CTGGAGGAATCTGTG | 7347 |
rs756636304 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602887 | GGATCAGTTGTTTAA[C/T]AATCTTAGTCTATAA | 7347 |
rs756675550 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584063 | CTCCTGTAGAACAAA[A/G]CCTAAAGACCTTGAG | 7347 |
rs756683677 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568487 | AGTGTATATATATAT[A/G]CACAATTTTTTAAAC | 7347 |
rs756745419 | snp | C/T | 1.66319e-05 | 0.00288369 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605718 | ATCATACTTTTTTTT[C/T]TCCTCCATAGGATGC | 7347 |
rs756790170 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558583 | TTAAAAGGCAATTTA[A/G]GTAGTCTTCTGATTT | 7347 |
rs756790602 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567363 | CAAAAGTTTGTGGGA[C/T]TGTAGATGTGTTTGG | 7347 |
rs756799062 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593397 | CTCATTATCACTGTC[C/T]TCACATATTTAAAGA | 7347 |
rs756892680 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583699 | AACCAGAAACAAACT[-/A]AAGGTGCAGTATTAC | 7347 |
rs756909784 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580040 | AAACATAATTGTTAA[A/G]CCAGTCAGGGAAAAA | 7347 |
rs756940543 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564798 | CCTCCTGGGTTCAAG[C/T]GATTCTCATGGCTCA | 7347 |
rs757110241 | snp | A/G | 1.86437e-05 | 0.00305311 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560905 | TATGTAAAATAGAAA[A/G]TTTCTGGTAAATACA | 7347 |
rs757111474 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552940 | TTATATGGACCCCTC[G/T]CCACCCCAAGGATTA | 7347 |
rs757164158 | snp | C/T | 3.30262e-05 | 0.0040635 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605808 | TTGCTCTTTCTGCAG[C/T]ATAGCTTGTCAATAA | 7347 |
rs757183978 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600252 | GCTGATGGAGAAGCT[A/G]CAAGTTATCCAGAAG | 7347 |
rs757249754 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588534 | GTATAGGATTCATTT[A/G]TGTATTTTTGATTGA | 7347 |
rs757328966 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589233 | TGTGCTCTGATTCCT[C/T]ATTTGCATAACAGGA | 7347 |
rs757331881 | snp | A/C | 1.7321e-05 | 0.00294282 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569550 | TTGCTATAAATTTAA[A/C]CATATAAATTTCTTG | 7347 |
rs757346726 | snp | C/G | 0.000483734 | 0.0155446 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590103 | CGACCCTTCTTACGT[C/G]TACCATCTTTGGGTC | 7347 |
rs757362049 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597038 | GTGGTAAAGAATAGC[C/T]ATAATCTTTGAGATG | 7347 |
rs757382777 | snp | C/T | 2.20437e-05 | 0.00331984 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549798 | CGGCGGCTGTCAGAG[C/T]TGGAGGGCCGGGCAC | 7347 |
rs757386558 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562922 | TAAATAGCATGTACT[A/G]CTTTTAGATGTCTTA | 7347 |
rs757470853 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549101 | CTTCATGCCATCACT[A/G]TCATATAGGTACCAC | 7347 |
rs757726253 | snp | A/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606013 | CTTTTCTTGTGAAGG[A/T]TTTATCTTGTTTGAA | 7347 |
rs757814524 | in-del | -/AA | 1.6492e-05 | 0.00287154 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567349 | TGATCTCATGTGGGC[-/AA]AAGTTTGTGGGATTG | 7347 |
rs757870650 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591155 | AGTCAATGGCAAGCA[C/T]TCTTTCCTTCCCCTT | 7347 |
rs757899868 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580451 | ACACATATGTGTACA[C/T]ACATTTATAATCTAA | 7347 |
rs757903004 | snp | C/T | 1.65225e-05 | 0.00287419 | missense | UCHL3 | GRCh38.p7 | 13:75567235 | TTCTCAGAATCTGGA[C/T]CAACCTTGAAAAAAT | 7347 |
rs757911552 | snp | A/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547308 | GCTCAACCTTGGCTG[A/G]GAACTACAATTTTTT | 7347 |
rs758010200 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554428 | CCATGAATGTCGGCT[A/G]TTTTTAATATTCTAT | 7347 |
rs758044233 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566315 | TATAGTATTCTATTA[C/T]GATATGCCATAATAT | 7347 |
rs758058182 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553142 | ATCATATAAATTCTC[A/T]TAAGAATTCTCTAAT | 7347 |
rs758061769 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582228 | TCAGAGGATTTAAAT[A/C]AGAATTAATGCTTAA | 7347 |
rs758088452 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75601363 | ACAGAGAAATCTTTC[A/G]TAAAAGAAAGAGTCA | 7347 |
rs758148252 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554279 | TCTGTTTCCCAGGCT[G/T]GTCTCAAATGCCTGG | 7347 |
rs758153494 | snp | C/T | 1.66899e-05 | 0.00288871 | utr-variant-5-prime, missense | UCHL3 | GRCh38.p7 | 13:75560783 | GGTCTACATCCTAAC[C/T]GGCAATTCGTTGATG | 7347 |
rs758165413 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602604 | CAAGTGACAGTTTTG[C/T]GGTAGTAGTGTTTGG | 7347 |
rs758238839 | snp | A/C | 1.69361e-05 | 0.00290994 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605708 | ACACTGAAAAATCAT[A/C]CTTTTTTTTTTCCTC | 7347 |
rs758257551 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575438 | GTTTTCTTTTTTTCC[A/G]TTGATTTTCCACTTG | 7347 |
rs758352791 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592437 | ATATATATATATATA[C/T]ATATATATATATATA | 7347 |
rs758418860 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576296 | GTGTAGTGGCGCAAT[A/C]TCTGCTCACTGCAAC | 7347 |
rs758470066 | snp | A/C | 1.67351e-05 | 0.00289263 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604739 | CTGTAAAAACAGCTA[A/C]GCATTCAATTGTTTG | 7347 |
rs758512946 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564497 | CATCTCCTTTACAAG[C/G]TGATTGTCTCCTTTG | 7347 |
rs758516693 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598603 | TTATCCTCCAATTTA[A/G]GCCATCTGATTTATC | 7347 |
rs758541008 | in-del | -/AACCATA | 3.44691e-05 | 0.00415131 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569548 | TCTTGCTATAAATTT[-/AACCATA]TAAATTTCTTGCTGT | 7347 |
rs758584070 | snp | A/G | 1.83971e-05 | 0.00303285 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560895 | AGGTAATTGTTATGT[A/G]AAATAGAAAGTTTCT | 7347 |
rs758587112 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557963 | GGACATTTTAATGAT[-/TT]TTTTTTTTTTTGAAG | 7347 |
rs758609818 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586163 | ATAACAATCAAAAGG[A/T]TGGGAAAAGATGAAC | 7347 |
rs758624116 | in-del | -/GA | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549994 | ACCAACCAGGTGAGT[-/GA]GGTGTCTGTCGCTCG | 7347 |
rs758626262 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587328 | CTAAGGAGACATGAT[A/G]AATAAATTTAATATC | 7347 |
rs758637977 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557380 | GGACCATAGAATAAA[A/G]AGAATAAGTTGACTG | 7347 |
rs758681503 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591253 | AATATCAGTATGGTC[A/G]TCAAATACTTTTCCA | 7347 |
rs758725841 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558129 | TAACAATATATTCAG[C/T]AGATATTAGTTGCAT | 7347 |
rs758831328 | snp | C/T | 2.3325e-05 | 0.00341496 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549793 | GAAGGCGGCGGCTGT[C/T]AGAGCTGGAGGGCCG | 7347 |
rs758880387 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593459 | AAGATGATGGAAAAT[A/G]CAAGGAGACATATTT | 7347 |
rs758887565 | snp | A/G | 0.000146242 | 0.00854982 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549828 | CCGCGGCCATGGAGG[A/G]TCAACGCTGGCTGCC | 7347 |
rs758896724 | snp | C/T | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606165 | AAAACATTTGTGAAG[C/T]GTCTACTTGTAACGA | 7347 |
rs759023184 | snp | A/C | | | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549472 | CACGCGGTCCCAGAC[A/C]GGCGCAAGGCGCATG | 7347 |
rs759054859 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566678 | CAAATACACTGTTGA[-/C]TTTTTTTTTTTAATA | 7347 |
rs759069179 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598032 | TAGAGTAGAGCATTG[A/G]GATTTAGAGGTGGAT | 7347 |
rs759120893 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564193 | TCTCGCTCTGTTGCC[C/G]AGGCTGGAGTGCAGT | 7347 |
rs759168597 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571720 | CAGTGATTCTCAAGA[C/T]GGAGTGCAGATAGAA | 7347 |
rs759224675 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553120 | CTTAAATAATCACAA[G/T]AAATAAATCATATAA | 7347 |
rs759227367 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549939 | CGCGAGTCCACGGTG[G/T]TTTGTCTCTAAAGCG | 7347 |
rs759272498 | snp | A/G | 2.41496e-05 | 0.0034748 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560710 | AGTTTTCTTTTACCA[A/G]CTAATGTTCCATTGT | 7347 |
rs759309420 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599135 | CACCATGCCTGGCTA[-/TT]TTTTTTTTTTTTTTT | 7347 |
rs759336246 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573109 | TCTCTACTAAAAATA[C/T]AAAAATCAGCTGGGC | 7347 |
rs759367213 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590595 | GGGGTTACTTTACTT[-/A]ACTCTATTCTCAATC | 7347 |
rs759404904 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567223 | TCTTCTTTCATATTC[C/T]CAGAATCTGGATCAA | 7347 |
rs759424443 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605471 | CGAGATTGCACCACT[A/G]CACTCCAGCCTGGGT | 7347 |
rs759468442 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585776 | TAATACTGTTGTGAG[G/T]TTCTTATACTACATA | 7347 |
rs759484896 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582423 | TACAGTCACATTATA[C/T]TGTTGCAGTGCCCAC | 7347 |
rs759494455 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567486 | TATCCACAAATGCTG[A/T]TAAGTTGCCATTTCT | 7347 |
rs759497621 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558293 | TAATTGGTATCACTA[C/G]AGTGGCTGCGTTTGG | 7347 |
rs759527742 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569765 | AATGCAGATTGTGTG[-/C]TGTTTGTGCGGCTTG | 7347 |
rs759586135 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600852 | GCTTTGATGGATCTG[A/C]GAATAGTAAATTGGA | 7347 |
rs759674174 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588405 | CCCCTATTCTTTCCT[C/T]CTCTCTTTCCTGTTA | 7347 |
rs759697887 | snp | A/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597581 | TTGTATTATGTATGA[A/T]AAGTAATCTAGAGAT | 7347 |
rs759808146 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589333 | GCATAAAAAAAGATG[C/T]GTATTATATTTAATG | 7347 |
rs759814929 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553908 | GTGATGAGTTGATGC[C/T]GTTGATTCTTCTTTC | 7347 |
rs759904664 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555040 | AAGGATAATGGCATC[C/G]AGCTCCATTTCAAGC | 7347 |
rs759928758 | in-del | -/ATAAAA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568404 | ACATCTTTATTATAC[-/ATAAAA]ATAAACATGAAAATC | 7347 |
rs759943625 | snp | C/T | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547143 | CTTGGGATTACTAAA[C/T]AGCAGTTGAGCACGA | 7347 |
rs759980579 | in-del | -/GAG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600377 | ACTTCTGTAGCTAGA[-/GAG]GAGATGTCAACACCT | 7347 |
rs760002431 | snp | A/G | 1.65211e-05 | 0.00287407 | missense | UCHL3 | GRCh38.p7 | 13:75569476 | CCATCCGAGTTACTC[A/G]TGAGACCAGTGCCCA | 7347 |
rs760051255 | snp | C/T | 1.85434e-05 | 0.00304489 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566685 | ACTGTTGACTTTTTT[C/T]TTTTAATAGTATGAA | 7347 |
rs760093778 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562660 | TTTTGTAAAAAATAA[A/C]TTAGATTTGATCTCT | 7347 |
rs760125280 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596566 | GAAAGTAGATTTGGC[C/T]AGAGCAAACATATGT | 7347 |
rs760137256 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571834 | AGTTTAGAAACACTA[-/C]TGGAGTGAGCAATAT | 7347 |
rs760215376 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571924 | GATTCCTCAAGCCTG[C/T]GCAGTCAGTTTCAGG | 7347 |
rs760217672 | in-del | -/CAGAA | 5.42834e-05 | 0.00520949 | frameshift-variant | UCHL3 | GRCh38.p7 | 13:75566706 | ATAGTATGAAGTATT[-/CAGAA]CAGAAGAGGAAGAAA | 7347 |
rs760249794 | snp | C/G/T | 3.73359e-05 | 0.00432051 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549822 | CGGGCACCGCGGCCA[C/G/T]GGAGGGTCAACGCTG | 7347 |
rs760303070 | snp | A/G | 1.65056e-05 | 0.00287272 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549895 | CAGCCCTGGGCCGTG[A/G]GCAGGTGCAGAGGGA | 7347 |
rs760307652 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558463 | TAAAATTGCTCTGTT[G/T]TATGTACCATCGTGT | 7347 |
rs760310101 | snp | G/T | | | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605773 | GGAGCGCGACCCTGA[G/T]GAACTAAGATTTAAT | 7347 |
rs760373304 | snp | A/T | 1.72113e-05 | 0.00293348 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566875 | TTTTTCATTACTGCA[A/T]TTTTTCCCCCTTAAG | 7347 |
rs760376518 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573381 | TTTTGTCAGTTCCTA[C/T]AAAATACATAGGTCT | 7347 |
rs760398789 | in-del | -/TT | 1.66449e-05 | 0.00288482 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595001 | ATTAGGTAAGAACTA[-/TT]TTAATTTGTCCTGGG | 7347 |
rs760455851 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559876 | GTTATCAGCTTCTTT[C/T]GATATAAAGTTATTA | 7347 |
rs760512471 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594322 | TCCCTTCCTTTTAAT[C/T]GCCTAGGCTATTTTC | 7347 |
rs760524598 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599136 | ACCATGCCTGGCTAT[-/T]TTTTTTTTTTTTTTT | 7347 |
rs760543650 | snp | A/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75546890 | AGCAAATACTAAATC[A/G]TTGCTTCTAGGGGAA | 7347 |
rs760544861 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581854 | AAAAGTAATTTGGCC[C/T]TTGAGGACGTAGGTG | 7347 |
rs760568114 | snp | A/C | 1.66932e-05 | 0.002889 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567202 | TATCAAGCCTTTTTA[A/C]TTTTATCTTCTTTCA | 7347 |
rs760600403 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595178 | TTATTTTATGTTTAA[C/G]CAACTTATAATTCAA | 7347 |
rs760602337 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555108 | TGACCCGCTCATGCT[A/G]TGCTGCAGTCTTCGA | 7347 |
rs760658162 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579897 | TCAAACTGTAAAGAA[A/G]ATAATTTCTGGGAAT | 7347 |
rs760710440 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592495 | ATCCCATCTATAGCC[-/TT]TTTTTTTTTTTTGCC | 7347 |
rs760792597 | snp | G/T | 1.6806e-05 | 0.00289875 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604874 | CAATATTTTGTCATC[G/T]TTAAAACATCTCTAA | 7347 |
rs760968115 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576895 | ATTTAAAAATGAATG[G/T]ATACAGTTGGCCCGC | 7347 |
rs760992753 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562791 | GAAGAACACAGTTCT[A/G]AAGTATTTGCGTAAG | 7347 |
rs761015496 | snp | C/T | 1.71997e-05 | 0.0029325 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560848 | ACCAAGACCAGTCTG[C/T]GCAGTCTTACTTCTC | 7347 |
rs761044970 | snp | A/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547307 | TGCTCAACCTTGGCT[A/G]GGAACTACAATTTTT | 7347 |
rs761103437 | snp | A/G | 1.65258e-05 | 0.00287448 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605761 | CAAGAAGTTTATGGA[A/G]CGCGACCCTGATGAA | 7347 |
rs761129744 | snp | A/T | 0.000116494 | 0.00763107 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560736 | ATTGTTTTTTTTTTC[A/T]TTCTTTCTTTTACCA | 7347 |
rs761240122 | snp | A/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550583 | CATTCTTTGCAATCT[A/G]TAGCAATTTAAGTTC | 7347 |
rs761309752 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580301 | GAACCTTAAATTTAC[-/T]GTAATCCAATGTATT | 7347 |
rs761343060 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574603 | CCTTATGGGATTGTT[G/T]TGAAGACTAATGAGT | 7347 |
rs761371610 | snp | C/G | 1.65111e-05 | 0.0028732 | missense | UCHL3 | GRCh38.p7 | 13:75569465 | CTTATTACAGGCCAT[C/G]CGAGTTACTCATGAG | 7347 |
rs761438196 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594544 | AACTTTCTTATTTCA[A/G]ATTTTAAAAACTCAT | 7347 |
rs761456680 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595371 | GGGAGGCTGAGGCAG[A/G]CGGATAACCTGAGCT | 7347 |
rs761532311 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559924 | CTCATTTTTTCTCTA[A/T]GTGATAGATTAAGGT | 7347 |
rs761550956 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582175 | CTCATAGCTCACTTT[C/G]TCTGTGTGTGTAAGT | 7347 |
rs761621879 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561235 | ACTGTTCCCAGCCCA[A/G]TTTCTTTTTCTTCTT | 7347 |
rs761622290 | snp | A/C | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547161 | CAGTTGAGCACGATG[A/C]TTGGGGGCCATTTTA | 7347 |
rs761672452 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589693 | CTGTGCTATGCAAAT[A/G]AGGATATGTGAATAT | 7347 |
rs761704103 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583419 | ATGCTCAAAAAGAAG[A/G]CTAAAATTACTAGTG | 7347 |
rs761782262 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567694 | CTAGGATTTCAGGTG[C/T]GTGGCACCACACCTG | 7347 |
rs761800362 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569566 | CATATAAATTTCTTG[C/G]TGTAAATTTAACCAT | 7347 |
rs761870184 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553946 | CATTCCAGAGAGGCC[G/T]TAGTATCTTGATTTG | 7347 |
rs761873410 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602398 | AAAAGTCAGGCCACT[A/G]TTTTCTTCCCCGTCC | 7347 |
rs761930908 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577008 | TAATGCCAGCACTTT[A/G]GGAGGCCAAGAAGGG | 7347 |
rs761941633 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547648 | ACATCCATACCAGAC[A/G]GTGTAGGTTAAACTG | 7347 |
rs761943255 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581150 | AAACAGTAATTATTT[G/T]AACTATCTACCCACT | 7347 |
rs762029977 | snp | A/C | | | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605885 | ATACACTAACTCAAA[A/C]ATTTTGATATTTTCA | 7347 |
rs762092202 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578471 | GTTTGAGCACCTACT[A/G]TACTAGGCACTGTGC | 7347 |
rs762109315 | in-del | -/A | 5.14293e-05 | 0.0050707 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605698 | AACACTTTTACACTG[-/A]AAAAATCATACTTTT | 7347 |
rs762120498 | snp | C/T | 2.00018e-05 | 0.00316236 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560727 | TAATGTTCCATTGTT[C/T]TTTTTTTCTTTCTTT | 7347 |
rs762139221 | snp | C/T | 1.6806e-05 | 0.00289875 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567189 | GGTCTCTCTGCTGTA[C/T]CAAGCCTTTTTAATT | 7347 |
rs762150081 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564441 | AGGTGTGAGCCACTA[C/T]GCCTGGCCTAAAGTG | 7347 |
rs762150228 | snp | A/G | 1.66054e-05 | 0.00288139 | missense, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604816 | GAAACTAGTGATGAA[A/G]CTTTATTAGAGGTAA | 7347 |
rs762170278 | snp | A/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550628 | AGGTTGGGGGTTGGG[A/G]AGGGAGGAGGGAACA | 7347 |
rs762211812 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599492 | GCACCATTTTTTCCA[A/G]CAGCATGTGCTCACT | 7347 |
rs762512699 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596514 | AAGAGGAAATAAAGA[G/T]TGCTGGGACTTAACA | 7347 |
rs762514285 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560199 | ATCTTTAAACCTCAG[A/T]CATCATTTTTGGTAA | 7347 |
rs762636889 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581985 | CTTATGAATCAGTCA[A/G]ATTAGTTGACAGTTG | 7347 |
rs762693275 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570360 | CCTGCCTCAGCCTCC[C/T]GAGTCGCTGGAACTA | 7347 |
rs762693521 | in-del | -/TTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581517 | ATCACACCTGGCTAA[-/TTT]TTTTTTTTTTTTTTT | 7347 |
rs762731654 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549331 | ACAGCACCGTGCTGC[A/T]CGGCGTCCTCCGGCC | 7347 |
rs762850661 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555151 | TTCCTGCTTCAGAGT[A/C]TTTGCACTTGCTCAT | 7347 |
rs762892642 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603657 | AGTCTATTGAAGAAT[A/C]AGCATTTACCACAAA | 7347 |
rs762931872 | snp | A/G | 1.86816e-05 | 0.00305622 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566691 | GACTTTTTTTTTTTA[A/G]TAGTATGAAGTATTC | 7347 |
rs762944925 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556761 | TCAGGAGTTCATTGT[G/T]GCCAAGTTAGAGAAT | 7347 |
rs763085224 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579713 | TGACTAGATGAAACT[C/T]GTCTAAGAATGCTTT | 7347 |
rs763137885 | in-del | -/G | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606509 | ACATCTTGCTGTATT[-/G]TAGGACCAGGAAGGA | 7347 |
rs763160768 | snp | A/C | 1.69052e-05 | 0.00290728 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566854 | AAGATGCACTTTGGT[A/C]AATGATTTTTCATTA | 7347 |
rs763170425 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600722 | AGAGATTAATATTTT[A/C]ATTTCTGCTAACACA | 7347 |
rs763325816 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567115 | CTTACATTTCTAACC[C/T]ACCAATGAAAGAATT | 7347 |
rs763335297 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574886 | GAGCTCAGGCGAGAT[A/T]TCTGGAGTCTTTGGT | 7347 |
rs763374002 | snp | C/T | 0.000118001 | 0.00768027 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590073 | ACCAGTCCATCTCTC[C/T]GTCTTCGTCGCTGGC | 7347 |
rs763419935 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589194 | TACTGGCAATGTGAC[C/G]TTGGTTATGTTACTT | 7347 |
rs763425963 | in-del | -/TT | 0.00114934 | 0.0239447 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605710 | ACTGAAAAATCATAC[-/TT]TTTTTTTTCCTCCAT | 7347 |
rs763427473 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560404 | AAGAGGTTTTATTTC[A/T]CATGTTATGAATGTT | 7347 |
rs763459962 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567357 | TGTGGGCAAAAGTTT[A/G]TGGGATTGTAGATGT | 7347 |
rs763571821 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576041 | ACAGGTGTGAGCCAC[C/T]GCCCCAGCCAAACAC | 7347 |
rs763578327 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557104 | CCTGTAGTCTCAGCT[A/G]TCTGGGAGGCTGAGG | 7347 |
rs763662069 | snp | C/T | 1.65086e-05 | 0.00287298 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569457 | CCTTTATTCTTATTA[C/T]AGGCCATCCGAGTTA | 7347 |
rs763677124 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572143 | TTTATTATTTCTATT[A/C]TTCTTGCAGTACTCT | 7347 |
rs763686924 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593225 | AATGAATAATTCATT[A/G]TAGCCTTTTTTATTA | 7347 |
rs763767071 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573530 | CAGGGTTGGCTTCTA[C/T]TGAGATGTCCCTTCC | 7347 |
rs763785631 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558503 | TTATAACAGGATGAC[G/T]TTGTGGGTACATAAA | 7347 |
rs763844137 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594323 | CCCTTCCTTTTAATC[A/G]CCTAGGCTATTTTCC | 7347 |
rs763937455 | snp | A/G | 4.95225e-05 | 0.00497582 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605791 | ACTAAGATTTAATGC[A/G]ATTGCTCTTTCTGCA | 7347 |
rs763998584 | snp | A/G | 1.84647e-05 | 0.00303842 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560898 | TAATTGTTATGTAAA[A/G]TAGAAAGTTTCTGGT | 7347 |
rs764105150 | in-del | -/TA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602917 | ATAATTGAAATTAAT[-/TA]TATGTTACTTTAAAC | 7347 |
rs764115149 | in-del | -/AAAACAAAAAC | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602119 | GTCTCAAAAAAAACA[-/AAAACAAAAAC]AAAACAAAAACAAAA | 7347 |
rs764125599 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556250 | TAATCCACACATAAA[G/T]TGTTTTCAGTGTTTC | 7347 |
rs764235668 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589606 | GTTACATGGTTTTTG[G/T]GTGTGTGTTACTTTT | 7347 |
rs764247200 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562822 | TAAATTTGTACTTAC[A/G]TAAGTAGAAAATGAT | 7347 |
rs764320440 | snp | C/G | 1.81807e-05 | 0.00301496 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549830 | GCGGCCATGGAGGGT[C/G]AACGCTGGCTGCCGC | 7347 |
rs764357718 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600601 | ACTGAATCTCTTAAG[C/T]CCTCTGTTGAGACGT | 7347 |
rs764416713 | in-del | -/CCGGC | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548005 | AAACTGTCTTGCTGT[-/CCGGC]CTTGTGTCTCAGCAG | 7347 |
rs764474703 | snp | A/C | 1.8231e-05 | 0.00301914 | missense | UCHL3 | GRCh38.p7 | 13:75566700 | TTTTTAATAGTATGA[A/C]GTATTCAGAACAGAA | 7347 |
rs764475282 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | UCHL3 | GRCh38.p7 | 13:75594940 | TAGATGAGAAAGTAG[A/G]TCTTCATTTTATTGC | 7347 |
rs764484496 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549561 | GGGCTGTGGATTCAG[A/G]TACTGTTTTTCTCCC | 7347 |
rs764526705 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549953 | GGTTTGTCTCTAAAG[C/T]GTGTTCTCTGTTTCG | 7347 |
rs764553436 | snp | G/T | 0.000119282 | 0.00772183 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590083 | CTCTCCGTCTTCGTC[G/T]CTGGCGACCCTTCTT | 7347 |
rs764569737 | in-del | -/AATCTGGATCAACCTTGAAAAAATTCCTGGAGGAATCTGT | 1.68783e-05 | 0.00290498 | splice-donor-variant | UCHL3 | GRCh38.p7 | 13:75566851 | ACAAGATGCACTTTG[lengthTooLong]GTAAATGATTTTTCA | 7347 |
rs764620515 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585855 | CTTGTAAATCCTCAG[A/G]CAATTACTGAAAAGC | 7347 |
rs764743569 | snp | C/T | 1.65315e-05 | 0.00287498 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75567231 | CATATTCTCAGAATC[C/T]GGATCAACCTTGAAA | 7347 |
rs764756364 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556945 | GATACACTGGGTTGA[A/G]TGCAGTGGTTCACAG | 7347 |
rs764985759 | snp | A/C | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548361 | GTCAAAGAACAGTGG[A/C]CAGAAGAACGTGGGT | 7347 |
rs764998716 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582196 | GTGTGTAAGTGAATG[A/T]GTGTGTGTGTTTAAA | 7347 |
rs765229797 | snp | A/G | 3.29614e-05 | 0.00405951 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567330 | CGGTACCTTCTTTCC[A/G]TTTTGATCTCATGTG | 7347 |
rs765238614 | snp | G/T | 1.86059e-05 | 0.00305001 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566688 | GTTGACTTTTTTTTT[G/T]TAATAGTATGAAGTA | 7347 |
rs765314162 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564445 | GTGAGCCACTACGCC[C/T]GGCCTAAAGTGCAGA | 7347 |
rs765365269 | snp | A/G | 0.00017141 | 0.00925612 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605698 | AAACACTTTTACACT[A/G]AAAAATCATACTTTT | 7347 |
rs765382416 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577017 | CACTTTGGGAGGCCA[A/G]GAAGGGAGGATCGCT | 7347 |
rs765444489 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547912 | GCTTCAACACATTTA[C/T]TGGGTGGTATGGAAA | 7347 |
rs765476975 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578578 | CTTTGAAAATCGCTT[G/T]CCAGTATTGAATTCC | 7347 |
rs765533437 | snp | A/G | 1.6522e-05 | 0.00287414 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605765 | AAGTTTATGGAGCGC[A/G]ACCCTGATGAACTAA | 7347 |
rs765657943 | snp | C/T | 3.30453e-05 | 0.00406467 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75569477 | CATCCGAGTTACTCA[C/T]GAGACCAGTGCCCAT | 7347 |
rs765667484 | in-del | -/T | 0.000118396 | 0.00769312 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569529 | CACATTTTTTCTAAA[-/T]TTTTCTTGCTATAAA | 7347 |
rs765678890 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552340 | CAGCAATATCCATCC[C/T]ACTCTCTTTTATTTC | 7347 |
rs765681310 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574856 | GTTTTTTTGGGTCAT[A/G]TGTGTAGGAGTCTAG | 7347 |
rs765711293 | snp | C/G/T | 5.54205e-05 | 0.00526381 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549786 | CGGCGGCGAAGGCGG[C/G/T]GGCTGTCAGAGCTGG | 7347 |
rs765712894 | snp | C/G | 0.000230441 | 0.0107316 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590040 | GTCAAACGTAACCAT[C/G]TAGGCCCTGCAAAGG | 7347 |
rs765777535 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595707 | TGATTTTTTAAAGAC[G/T]TTACAGGAGCCTTTG | 7347 |
rs765829847 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555713 | TCATTCTCATTGAAA[-/C]CATAGAGTAAATCTA | 7347 |
rs765860901 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582494 | GGCAAACATTGGTGT[C/T]GTTAATAGTTTTGAT | 7347 |
rs765944325 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568049 | CAGTGTAATAAAGGC[C/T]ACATAAACTAGGCTA | 7347 |
rs765982724 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560336 | CCAACTTATATGTAT[C/T]TGATGAAGTCCAGGC | 7347 |
rs766041145 | snp | C/G | 6.65281e-05 | 0.00576711 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567209 | CCTTTTTAATTTTAT[C/G]TTCTTTCATATTCTC | 7347 |
rs766189484 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75602610 | ACAGTTTTGTGGTAG[C/T]AGTGTTTGGAACAAC | 7347 |
rs766250603 | in-del | -/TTCTTTAAC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572068 | TTTCTTTCCTTCCTT[-/TTCTTTAAC]TTGTCTTTCTAACTT | 7347 |
rs766289931 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556843 | ATAGGTGCCATAGTG[G/T]TCAGATCCTTGCATG | 7347 |
rs766381328 | snp | G/T | 1.72e-05 | 0.00293253 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566878 | TTCATTACTGCATTT[G/T]TTCCCCCTTAAGATA | 7347 |
rs766383129 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591415 | CACAGTGAGAGATAC[A/C]AGGTGAACTAAATGA | 7347 |
rs766432773 | snp | G/T | 1.73267e-05 | 0.0029433 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605681 | TTTATCATTTGTAAG[G/T]AAAACACTTTTACAC | 7347 |
rs766449644 | snp | C/T | 0.000135639 | 0.00823415 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560739 | GTTTTTTTTTTCTTT[C/T]TTTCTTTTACCAGTT | 7347 |
rs766467942 | in-del | -/G | 1.6531e-05 | 0.00287493 | frameshift-variant, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605758 | TTGCAAGAAGTTTAT[-/G]GAGCGCGACCCTGAT | 7347 |
rs766472028 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600790 | AGACTTTCATTTCTT[G/T]TTATTTAAGAAATAC | 7347 |
rs766497883 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599792 | TAATAACCCTACAAA[G/T]GCCTGTAAGCATTCA | 7347 |
rs766503858 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553002 | AAAATATTTTCTAGC[A/G]TAATACCGAAAGGGA | 7347 |
rs766548631 | snp | A/G | 1.67089e-05 | 0.00289035 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595010 | GAACTATTTTAATTT[A/G]TCCTGGGGAGAGAAA | 7347 |
rs766604942 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565877 | TAATTTGCTAAAGTC[A/G]CACAGCTAATAACAG | 7347 |
rs766692807 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552614 | GTCAGCCCTTTTAAG[G/T]ATACTGTGTTATGCT | 7347 |
rs766709600 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588366 | CATTTATTTCCCCTT[G/T]TTATTCATTGCCTCT | 7347 |
rs766778251 | snp | G/T | 3.3089e-05 | 0.00406736 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569415 | TTCATTTAAAAAGTT[G/T]AGTATAGGCATTTTT | 7347 |
rs766813727 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576159 | AGCTTGGGATAGGAA[A/G]CAGATTGTGTGAGAA | 7347 |
rs766825486 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561652 | GGAATCACTAAGCTT[A/G]AATATATTTTAATTG | 7347 |
rs766851378 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560524 | TTTACTGAAGTATAA[C/T]TGACAAAAATTGAAC | 7347 |
rs766927044 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597308 | AGGCTACAGTGTGCT[A/G]TGATTGCACCTGTGA | 7347 |
rs766935654 | snp | C/T | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547356 | TGTGAGTGACCACGA[C/T]AACTTTGTGAGTATA | 7347 |
rs767104331 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75598158 | TTTATTTTGAAGTAA[C/T]TTAAGATGTTTGTAG | 7347 |
rs767112154 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604543 | ATTGTAATAAATTCC[A/G]TTCATGAAGATAATT | 7347 |
rs767131672 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571729 | TCAAGATGGAGTGCA[G/T]ATAGAAGTTAGGATT | 7347 |
rs767192926 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566667 | GTTATTTTCCACAAA[A/T]ACACTGTTGACTTTT | 7347 |
rs767223540 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556982 | AGCACTTTGGGAGGC[C/T]GGGGCCAGAGGATTG | 7347 |
rs767275311 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592944 | GCTCATTTAAACCTC[A/G]AGGTGGATAAGAAAC | 7347 |
rs767289613 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578869 | ATGTGTGTGTTTGTG[G/T]GGGTGTGTATATTTT | 7347 |
rs767313704 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591473 | TCTGACATGAGCACA[A/G]TTGATCCAATTCTAA | 7347 |
rs767343926 | snp | C/T | 3.30246e-05 | 0.0040634 | stop-gained | UCHL3 | GRCh38.p7 | 13:75569466 | TTATTACAGGCCATC[C/T]GAGTTACTCATGAGA | 7347 |
rs767370396 | snp | C/T | 1.66529e-05 | 0.00288551 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75566736 | AGAAAAAATAAAATC[C/T]CAGGGACAAGATGTT | 7347 |
rs767423288 | snp | G/T | 6.84791e-05 | 0.00585106 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566872 | TGATTTTTCATTACT[G/T]CATTTTTTCCCCCTT | 7347 |
rs767506320 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75602094 | AGCCTGGGCGACAGA[A/G]CGAGACTCTGTCTCA | 7347 |
rs767511925 | snp | A/G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579731 | CTAAGAATGCTTTCA[A/G/T]CAATAAAAATAGAAC | 7347 |
rs767591550 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600379 | TTCTGTAGCTAGAGA[C/G]GAGATGTCAACACCT | 7347 |
rs767594664 | snp | A/G | 3.29913e-05 | 0.00406135 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75594959 | TCATTTTATTGCATT[A/G]GTTCATGTAGATGGG | 7347 |
rs767610216 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597703 | GGTATGAGATGGGGC[C/T]GGTGTCCTGGAACCA | 7347 |
rs767649698 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553640 | CTTGCCCTAGTAATG[-/T]TTTCTGTTGTATAGT | 7347 |
rs767746230 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553909 | TGATGAGTTGATGCC[A/G]TTGATTCTTCTTTCA | 7347 |
rs767830923 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588364 | ATCATTTATTTCCCC[C/T]TTTTATTCATTGCCT | 7347 |
rs767846492 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576266 | GTGAAGTCTCGCTCT[G/T]TCTCCCAGGCTGGAG | 7347 |
rs767900733 | snp | A/T | 0.000357839 | 0.0133713 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560734 | CCATTGTTTTTTTTT[A/T]CTTTCTTTCTTTTAC | 7347 |
rs767938373 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561766 | TTTTCTAGAATGATA[C/T]ATGTGTATGTTTCTG | 7347 |
rs767954986 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562688 | TCTTTCATTTAGTGA[A/G]TCATCAGCATTAAAA | 7347 |
rs767972626 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549971 | GTTCTCTGTTTCGTT[C/T]TCAGGTCACCAACCA | 7347 |
rs768013145 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548632 | CATTTATTTCTCACA[C/T]GTTTTTCACATTATT | 7347 |
rs768100301 | snp | A/C | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596602 | TCATAACCAGAGACT[A/C]TAAATCTGATTGTGA | 7347 |
rs768105984 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553303 | CACATTCTTTTCCTT[A/G]TTCATTCCTGTGTAG | 7347 |
rs768140232 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588779 | CAAAATCTATTATCA[C/G]CAAGCAAGGATTTAT | 7347 |
rs768156506 | in-del | -/TT | 5.01086e-05 | 0.00500517 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604751 | CTAAGCATTCAATTG[-/TT]TGTCTGTTTTCCACA | 7347 |
rs768187109 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600444 | TGTTAATGCAGACGG[C/T]GACTTTCAGTTGAAG | 7347 |
rs768239029 | snp | C/T | 3.45393e-05 | 0.00415554 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566651 | CTGAGTTTTTTAATA[C/T]GTTATTTTCCACAAA | 7347 |
rs768450192 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575756 | ACAAACACTTTCTTT[A/C]TTTTTTGTTTTTTGA | 7347 |
rs768458081 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559879 | ATCAGCTTCTTTCGA[C/T]ATAAAGTTATTAATT | 7347 |
rs768466758 | snp | C/G | 1.64925e-05 | 0.00287158 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594901 | ATAATACCTATTTTT[C/G]CCTCCTATTCCAGGC | 7347 |
rs768490131 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549199 | CAATACTTAGTACAG[C/T]GATTTCTAGTACTCG | 7347 |
rs768531007 | snp | G/T | 0.000164867 | 0.00907779 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589895 | ATAAATGATCACCCA[G/T]TAACGTGGTCTAAGT | 7347 |
rs768599459 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583246 | TACAATATATTGATA[C/T]GCTATCCTATTTTGA | 7347 |
rs768632595 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548121 | AACCTCAGGGATCTG[A/G]AACAAGGCAATTCCT | 7347 |
rs768663548 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556573 | TTTTTTTAATTTATA[A/G]AATCAGAGTTTTTGT | 7347 |
rs768769111 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572631 | TTAATTAACCAGAAT[G/T]AGCTCAGAACTGTCC | 7347 |
rs768831713 | snp | A/G | 3.39219e-05 | 0.00411823 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566858 | TGCACTTTGGTAAAT[A/G]ATTTTTCATTACTGC | 7347 |
rs768876397 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560018 | GTTATTTTGCCAGAT[A/G]TAAGAGAGGCAATGA | 7347 |
rs768886958 | snp | C/T | 1.68357e-05 | 0.00290131 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567179 | TTCATATATTGGTCT[C/T]TCTGCTGTATCAAGC | 7347 |
rs768902862 | snp | C/T | 1.65987e-05 | 0.00288082 | synonymous-codon, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604809 | CCATGGTGAAACTAG[C/T]GATGAAACTTTATTA | 7347 |
rs768913322 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605207 | AAAAGTTTCTTAATA[A/G]CATTTTAAGAACACT | 7347 |
rs768918574 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557590 | CTGCTTGATGTAAAT[A/G]GGATGCTTCTAATTA | 7347 |
rs768949201 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578076 | CTTTTTGCATCTATG[C/T]ATATTTGCTACCATT | 7347 |
rs769026045 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593708 | ATGTTGAATTTCTTC[C/T]GTTCATAATTTGAGG | 7347 |
rs769130927 | in-del | -/GGCGGCGGCGGCGAA | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549780 | GGCGGCGGCGGCGAA[-/GGCGGCGGCGGCGAA]GGCGGCGGCTGTCAG | 7347 |
rs769225644 | in-del | -/TCTTGTCTTTACTTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572019 | TCTTGTCTTGTCTTG[-/TCTTGTCTTTACTTT]TCCTTCCTTCCTTCC | 7347 |
rs769249250 | in-del | -/AAG | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587711 | AATTATTTTTTTAAA[-/AAG]AAGTTTTCAAAAAGG | 7347 |
rs769387377 | snp | A/G | 2.38547e-05 | 0.00345352 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560714 | TTCTTTTACCAACTA[A/G]TGTTCCATTGTTTTT | 7347 |
rs769456810 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596369 | CAGTTTTGAAGATGT[A/G]CCTTGCTAATTGAGT | 7347 |
rs769465288 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549287 | CAGACAAGGCCAACC[C/T]ATCACTCCTGCACCC | 7347 |
rs769493001 | in-del | -/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558549 | TAAATTCTCTTATCA[-/G]GGTTCATGATACTTT | 7347 |
rs769551976 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561281 | GTTTTTGATAAATAC[A/C]ATCTTTAAGAACAAA | 7347 |
rs769574330 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562417 | TTGTAGAAGAGTTGA[A/G]ACAAAAACTTAAGTT | 7347 |
rs769668976 | in-del | -/T | 0.0225677 | 0.1038 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560725 | ACTAATGTTCCATTG[-/T]TTTTTTTTTCTTTCT | 7347 |
rs769701429 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597432 | TCATTTCAAAGTTCA[A/G]TTTGCTCTCTGTGGG | 7347 |
rs769730327 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591935 | ACAATGCTGCAGTTA[A/G]CATTTCCTTTGAACA | 7347 |
rs769744064 | snp | C/G | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606481 | TAATGAATGTGGAGT[C/G]CCTAAAGTAGGAACA | 7347 |
rs769752415 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571354 | TCTTTTTTCAGACCT[A/G]ACCGCCTTCATTCTT | 7347 |
rs769833633 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75593938 | CTGTTACTGAAAGGA[C/T]ATTAAGTAATCTGAG | 7347 |
rs769912226 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559214 | CCAGCTAATTTTTTT[A/G]TATTTTTAGTAGAGA | 7347 |
rs770002848 | snp | A/C | | | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75594980 | TGTAGATGGGCATCT[A/C]TATGAATTAGGTAAG | 7347 |
rs770020121 | snp | A/T | 1.74309e-05 | 0.00295214 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566893 | TTTCCCCCTTAAGAT[A/T]CAAGTTAATTGCATT | 7347 |
rs770081254 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579615 | TTTTCTGATCTCAGA[A/C]TTTTAGAAATGGAGA | 7347 |
rs770084920 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565561 | TCTGTAAAGGACTAG[A/G]TAGTAAATATTTTCA | 7347 |
rs770204302 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600645 | AGATTCCTTTGAAAA[C/T]ATTACTGCTAATTGA | 7347 |
rs770238359 | in-del | -/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597066 | ATGTCAGAGCAATAA[-/T]AGGTACATTACAAAG | 7347 |
rs770330271 | snp | A/C | 1.72821e-05 | 0.00293951 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566882 | TTACTGCATTTTTTC[A/C]CCCTTAAGATACAAG | 7347 |
rs770358564 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589086 | GTTAGCATTAACATA[C/T]TTTTCTTGGTCACTT | 7347 |
rs770411447 | in-del | -/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598633 | CTCATGATTTATGCA[-/T]TTTTTGGCAGGAATA | 7347 |
rs770478654 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563775 | TCTGTTTCGTTCTCT[A/G]TGTATTTGAGCTTTT | 7347 |
rs770497117 | snp | C/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550315 | TGTTAGTGCCGATTC[C/T]ATAATTTTCCTACCG | 7347 |
rs770516108 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562619 | CTGAATTGGAAATTT[C/G]CAAACCATTGATTTT | 7347 |
rs770537476 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592288 | TTATACTAAAAGAGT[A/G]GGATCCTTATCAGTA | 7347 |
rs770547010 | snp | A/G | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604769 | GTCTGTTTTCCACAG[A/G]TGGGCGGAAGCCATT | 7347 |
rs770547075 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549929 | GGCTTGCTGCCGCGA[A/G]TCCACGGTGGTTTGT | 7347 |
rs770598441 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550037 | TCTTTTCTGTCTGCT[C/T]GGTCCGCTTCCCTGC | 7347 |
rs770606143 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549405 | TAGGACTCCGCGGCA[C/T]GCCTCCTAGCGCAGT | 7347 |
rs770736822 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592659 | AATTGAAGCTGACTG[A/T]AGGAAAGGGCTTATC | 7347 |
rs770765532 | snp | A/G | 3.29554e-05 | 0.00405914 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567316 | GAGAACTATGATGTC[A/G]GTACCTTCTTTCCGT | 7347 |
rs770776286 | snp | A/G | 3.29772e-05 | 0.00406048 | missense | UCHL3 | GRCh38.p7 | 13:75594924 | TTCCAGGCACCAAGT[A/G]TAGATGAGAAAGTAG | 7347 |
rs770800210 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586433 | ACAATTATAGTTGGA[C/G]ATGTCAACACTCAGA | 7347 |
rs770805908 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573983 | AGTACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 7347 |
rs770840129 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569849 | AATACCTGCACTGTT[G/T]TACAGTTAAATAGCC | 7347 |
rs770865574 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605337 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7347 |
rs770887855 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572850 | GACCTCTAGTTGCCA[C/T]ATGTTAGTGTCTCCC | 7347 |
rs770928527 | snp | C/T | 3.3048e-05 | 0.00406484 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605762 | AAGAAGTTTATGGAG[C/T]GCGACCCTGATGAAC | 7347 |
rs770949650 | in-del | -/A | 0.000264795 | 0.0115034 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566677 | ACAAATACACTGTTG[-/A]CTTTTTTTTTTTAAT | 7347 |
rs770950201 | snp | A/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547685 | CCATATAAACCAGAC[A/G]GTGGAAGTTAAAATG | 7347 |
rs770983610 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581792 | TTAAAGAGTAATTTA[C/T]TCATTTTTTGCTGTA | 7347 |
rs771002799 | in-del | -/T | 0.174966 | 0.238474 | intron-variant | UCHL3 | GRCh38.p7 | 13:75590178 | GTGACAAGGGCTGTC[-/T]TTTTTTTTTTTTTTT | 7347 |
rs771069380 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585470 | TTGAGACAGACAAAA[A/G]CTGAGAGAGCTCATA | 7347 |
rs771108867 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596078 | CATTAATTTTAAGTT[A/G]TATAAAGATAGAAGA | 7347 |
rs771129078 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583097 | AAAAATTTAGAATTA[G/T]TGATTCTAATGTTTT | 7347 |
rs771177741 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577267 | AAAAGAGAAAAAATA[-/T]TTGGAAAAAAAAGAT | 7347 |
rs771265198 | snp | C/T | 8.85347e-05 | 0.00665278 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566663 | ATATGTTATTTTCCA[C/T]AAATACACTGTTGAC | 7347 |
rs771269475 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603080 | CTGCGTCCTTGAACT[C/T]CTGGGCTCAAGTGAT | 7347 |
rs771309775 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568704 | TTAATAAATACTGCA[A/T]GGTACATCATTGTAG | 7347 |
rs771320095 | snp | C/T | 4.95013e-05 | 0.00497475 | missense | UCHL3 | GRCh38.p7 | 13:75566804 | ATGCCTGTGGAACAA[C/T]TGGACTGATTCATGC | 7347 |
rs771352972 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589205 | TGACCTTGGTTATGT[C/T]ACTTAACCCATTTGT | 7347 |
rs771372005 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558007 | AAAGTTGACCCTCTT[A/C]TCTACCCTTTCTCCA | 7347 |
rs771475208 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554990 | ACAAGTGAGAACATG[C/T]GGTATTTGGTTTTCT | 7347 |
rs771533180 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570080 | TTCCTTCCCCCCAGC[C/T]CTGACTGTATCACTC | 7347 |
rs771622707 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564988 | GGTGTGAGCTACTGC[A/G]CCCGGCCAGTGATAG | 7347 |
rs771659221 | snp | C/T | 0.000348898 | 0.0132033 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75589945 | TTATGTAGTCCTCCT[C/T]GCCATCCTCATCACA | 7347 |
rs771708854 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551650 | GTTGCAAAGCTGGTT[C/T]ACCATTCAAAAATCA | 7347 |
rs771763550 | snp | A/C | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598905 | ACATTAGAAGCTTTC[A/C]TTTTCCTCTCATTTA | 7347 |
rs771783581 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600372 | CTAGGACTTCTGTAG[C/T]TAGAGAGGAGATGTC | 7347 |
rs771911593 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561160 | GTCTGGTCTCCAACT[C/T]GGGCTCAAGTGATCC | 7347 |
rs771942997 | in-del | -/ATATC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75601032 | AGGAAGTAACTGCAG[-/ATATC]ATGAAAATAGCAAGA | 7347 |
rs771962822 | snp | A/G | 3.3089e-05 | 0.00406736 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549887 | CTTCGGGGCAGCCCT[A/G]GGCCGTGGGCAGGTG | 7347 |
rs771979508 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594252 | GTTAAGCATCAAAGC[A/G]AGAGAAAAATCACAG | 7347 |
rs772088381 | in-del | -/TGTCTTGTCT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571977 | AAGTTTTCCTAACCC[-/TGTCTTGTCT]TGTCTTGTCTTGTCT | 7347 |
rs772092825 | in-del | -/TTTATGTATGTATGTATGTA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563126 | GGTACCTCATTATCC[-/TTTATGTATGTATGTATGTA]TGTATGTATGTATGT | 7347 |
rs772137217 | in-del | -/A | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597731 | CAGTCCCCCACAGAT[-/A]ATGGAGAGATGACTG | 7347 |
rs772171377 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555043 | GATAATGGCATCCAG[C/T]TCCATTTCAAGCTTT | 7347 |
rs772174909 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584620 | GGCTTTTAACCAAAA[A/G]CATTCAGCAGAGCTA | 7347 |
rs772296406 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603315 | AATGACACACACACA[C/G]AAATGATGGAAACCA | 7347 |
rs772328964 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571085 | TTATATGATCCTGAA[C/T]ATATTCATAATCTTC | 7347 |
rs772334492 | in-del | -/TTCC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572032 | GTCTTGTCTTTACTT[-/TTCC]TTCCTTCCTTCCTTC | 7347 |
rs772345560 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556104 | CTGAGTAATCTATGT[C/T]GAGTACAGTGGGCTA | 7347 |
rs772354880 | snp | A/G | 1.70182e-05 | 0.00291699 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560833 | ACTCCTTAGCATGGT[A/G]CCAAGACCAGTCTGT | 7347 |
rs772394608 | snp | A/C | 1.68057e-05 | 0.00289872 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567190 | GTCTCTCTGCTGTAT[A/C]AAGCCTTTTTAATTT | 7347 |
rs772405094 | snp | A/G | 1.65288e-05 | 0.00287474 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605759 | TGCAAGAAGTTTATG[A/G]AGCGCGACCCTGATG | 7347 |
rs772412344 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558426 | ATATTCTAACTGTGA[C/G]TTTTAGTTTGCAGCA | 7347 |
rs772457948 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590917 | TCATAATTGAGATAC[A/G]CTACAGAATTAAGCA | 7347 |
rs772458113 | snp | C/T | 1.65817e-05 | 0.00287933 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605844 | ACACCAAAAACTGTA[C/T]TATTTGCAACTAAAT | 7347 |
rs772512865 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577911 | CAGATATGGGTAGAG[A/G]TCACCTTATGATTTA | 7347 |
rs772538549 | snp | C/T | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605055 | AAGGCAAGAATAGTA[C/T]TGAAAGACTTGCTCA | 7347 |
rs772541882 | snp | A/T | 1.87503e-05 | 0.00306183 | intron-variant, upstream-variant-2KB, missense | UCHL3, COMMD6 | GRCh38.p7 | 13:75549821 | CCGGGCACCGCGGCC[A/T]TGGAGGGTCAACGCT | 7347 |
rs772591240 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576003 | GTGATCTGACTACCT[C/T]GGCCTCCCAAAGTGC | 7347 |
rs772647324 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579518 | AATAGAGGCCTTCCC[-/T]TTCCCCTTTTCTCTC | 7347 |
rs772692702 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592094 | GGTATGTATTAAGTG[C/T]TATACAATTATACAT | 7347 |
rs772743977 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590568 | GCATGACTTTAGTCT[C/G]TTGCCATGCTCTGGG | 7347 |
rs772790477 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576474 | GACCTCGTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 7347 |
rs772792014 | snp | C/T | 3.29766e-05 | 0.00406045 | missense | UCHL3 | GRCh38.p7 | 13:75594919 | TCCTATTCCAGGCAC[C/T]AAGTATAGATGAGAA | 7347 |
rs772858999 | in-del | -/TTTC | 9.93878e-05 | 0.00704869 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560732 | TTCCATTGTTTTTTT[-/TTTC]TTTCTTTCTTTTACC | 7347 |
rs772889785 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585174 | TCAGGAATCTCAGAG[A/G]CACTAGGTAGGATGA | 7347 |
rs772902085 | in-del | -/ACAA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552069 | AGATGATATAAACAG[-/ACAA]ACAATGTTATTTAGT | 7347 |
rs772956092 | snp | C/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548445 | TCTGACTCCCTAACT[C/G]CTCTCTACCTGAATT | 7347 |
rs773031541 | snp | C/T | 0.000113141 | 0.0075205 | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75589984 | CTAGCCACTGCAGAA[C/T]GAAGGCCTCATCATT | 7347 |
rs773050837 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583656 | TAGATACTTGTGTGC[A/G]CATTTTCACTAAAGC | 7347 |
rs773082118 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571499 | TTTCTGTTTCTTACA[A/G]TAGTTCCACCATACT | 7347 |
rs773197990 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549891 | GGGGCAGCCCTGGGC[C/T]GTGGGCAGGTGCAGA | 7347 |
rs773211155 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552829 | TTTATGACCGTACTA[A/G]ATCTTCATTGTGATT | 7347 |
rs773346837 | snp | C/T | | | intron-variant, downstream-variant-500B | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604308 | TTTGGATTATTCCTC[C/T]ATATTACTGCATTGA | 7347 |
rs773414852 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552479 | ATGCCTAGTGTTGTA[A/T]AAGAATGGCCATCAC | 7347 |
rs773497877 | snp | C/G | 1.7058e-05 | 0.0029204 | missense | UCHL3 | GRCh38.p7 | 13:75560835 | TCCTTAGCATGGTAC[C/G]AAGACCAGTCTGTGC | 7347 |
rs773518568 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581436 | CTCCCTGTAGCCTTG[A/C]TCTCCTGGGCTCAAA | 7347 |
rs773598077 | snp | A/C | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75601733 | GCTAACCCACAGTAT[A/C]TCTCAGGCATGCCTG | 7347 |
rs773601791 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588326 | TATTTATTAGTCACC[A/T]CTCCTTCTATCTCTT | 7347 |
rs773657524 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570764 | GAGTAATAAAAATTA[A/G]CCAGGTGTGGTGGTG | 7347 |
rs773674690 | snp | C/T | 1.65097e-05 | 0.00287308 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75569462 | ATTCTTATTACAGGC[C/T]ATCCGAGTTACTCAT | 7347 |
rs773677351 | snp | A/G | 1.67293e-05 | 0.00289212 | intron-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604861 | GGCCCATCTTCATCA[A/G]TATTTTGTCATCTTT | 7347 |
rs773681226 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553685 | TTGTCACATAGATGA[C/G]CCCATGTTCCTTGAA | 7347 |
rs773730866 | snp | A/C | 1.65269e-05 | 0.00287457 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605760 | GCAAGAAGTTTATGG[A/C]GCGCGACCCTGATGA | 7347 |
rs773731770 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562638 | ACCATTGATTTTTTA[C/T]GACTTTTTTTGTAAA | 7347 |
rs773750152 | snp | C/G | | | upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549445 | CTGCAAGAATGGGAA[C/G]GTGCGGGTGACCACG | 7347 |
rs773773668 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554728 | GGTCTTCCAATGCTT[G/T]TCCTTAGAAGATACT | 7347 |
rs773877872 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564182 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 7347 |
rs773940830 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594435 | TTGAAACATCAGATT[A/G]TCAAGTTCAAGTCTT | 7347 |
rs773998678 | in-del | -/CT | 0.00896843 | 0.066361 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566678 | CAAATACACTGTTGA[-/CT]TTTTTTTTTTAATAG | 7347 |
rs774027032 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581518 | TCACACCTGGCTAAT[-/TT]TTTTTTTTTTTTTTT | 7347 |
rs774103214 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585417 | ATTTTTAGAAAGCTG[A/C]GTTCAGTGGAACAAA | 7347 |
rs774225440 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558155 | TGCATTGAATTTCTT[C/T]ATATCTATCTCATTT | 7347 |
rs774312458 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554970 | GTTCTCATCATTTAG[C/T]TCTCACAAGTGAGAA | 7347 |
rs774339956 | snp | A/G | 0.0001628 | 0.00902073 | intron-variant | UCHL3 | GRCh38.p7 | 13:75589900 | TGATCACCCAGTAAC[A/G]TGGTCTAAGTAAAAT | 7347 |
rs774355792 | in-del | -/ATT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552804 | AGTGTGATATAGGCA[-/ATT]ATTATTATTTATGAC | 7347 |
rs774387983 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568870 | TTGCTATTTATAAAG[A/C]TTGTACTTTCACCTG | 7347 |
rs774470376 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75547693 | ACCAGACGGTGGAAG[C/T]TAAAATGTACAGTTT | 7347 |
rs774476958 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581816 | TGCTGTATAAAAAAG[G/T]GCATGCACACTAACT | 7347 |
rs774503890 | snp | A/T | 1.68278e-05 | 0.00290062 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567180 | TCATATATTGGTCTC[A/T]CTGCTGTATCAAGCC | 7347 |
rs774577407 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75567470 | TCAGATAACTTTGAA[A/G]TATCCACAAATGCTG | 7347 |
rs774669474 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553859 | CTTTTCTTCCCCATC[C/T]TCCAAGGGCATAGCC | 7347 |
rs774674375 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553119 | CCTTAAATAATCACA[A/G]TAAATAAATCATATA | 7347 |
rs774684412 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589291 | GTTAAATGAACCTAT[A/T]TATGTCAAGTCCTTA | 7347 |
rs774702454 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576197 | ATTGATAGCTTTTCA[C/G]TTACTCCTGAATTTT | 7347 |
rs774717261 | snp | A/C | 6.64132e-05 | 0.00576213 | missense, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604814 | GTGAAACTAGTGATG[A/C]AACTTTATTAGAGGT | 7347 |
rs774805641 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75598987 | ATAATCCATGATATC[A/T]TGTATTTTTATGCTC | 7347 |
rs774830695 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554991 | CAAGTGAGAACATGC[A/G]GTATTTGGTTTTCTG | 7347 |
rs774842832 | in-del | -/TTTG | 3.30033e-05 | 0.00406209 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594865 | TGTATACATGACTGA[-/TTTG]TTTGACTACTAATGT | 7347 |
rs774951865 | snp | A/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550579 | ACGCCATTCTTTGCA[A/G]TCTATAGCAATTTAA | 7347 |
rs775041670 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551799 | CCTTGTTTCTAGGGT[A/G]TCTTGAAAAACTATC | 7347 |
rs775053154 | snp | C/T | 1.69123e-05 | 0.0029079 | missense | UCHL3 | GRCh38.p7 | 13:75560822 | ATGGATCCTGAACTC[C/T]TTAGCATGGTACCAA | 7347 |
rs775165683 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559857 | GTAATGATGTACTTA[A/C]AAAGTTATCAGCTTC | 7347 |
rs775169578 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594278 | CACAGGCTACTGTGA[A/G]TTGTACTTTAATTTG | 7347 |
rs775199846 | snp | C/T | 7.12513e-05 | 0.0059683 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560718 | TTTACCAACTAATGT[C/T]CCATTGTTTTTTTTT | 7347 |
rs775248881 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596877 | AGGATTTTAAAATTG[G/T]TTTGAAGTAAGAACT | 7347 |
rs775328277 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75587956 | TCCACCCTAGCTCTG[C/T]CTGTTGCTCTCATGT | 7347 |
rs775332422 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573179 | TGAGGCGGGAGAATC[A/G]CTTGAACTCGGGAGG | 7347 |
rs775351582 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558432 | TAACTGTGACTTTTA[A/G]TTTGCAGCACAGATG | 7347 |
rs775352803 | in-del | -/TT | 0.490656 | 0.0677104 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566679 | AAATACACTGTTGAC[-/TT]TTTTTTTTTAATAGT | 7347 |
rs775368715 | in-del | -/TC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589677 | ATTAATTTCCATGAG[-/TC]TGTGCTATGCAAATG | 7347 |
rs775379563 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567341 | TTCCGTTTTGATCTC[A/G]TGTGGGCAAAAGTTT | 7347 |
rs775424803 | snp | C/T | 1.65105e-05 | 0.00287315 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569445 | TTCCAATGAATACCT[C/T]TATTCTTATTACAGG | 7347 |
rs775446956 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595126 | TTGATTTGACATAGC[A/G]ACAGTTTTCCTTTTA | 7347 |
rs775532072 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75556164 | AAGCAAACTAACATT[G/T]TATCACCTTTGTTGG | 7347 |
rs775613653 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591057 | TTTATAAGAAATTTG[A/G]CATTTCTATAAATTA | 7347 |
rs775637724 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569546 | TTTCTTGCTATAAAT[C/T]TAACCATATAAATTT | 7347 |
rs775654170 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555054 | CCAGCTCCATTTCAA[A/G]CTTTTATCATGGCTG | 7347 |
rs775707618 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576864 | ATAACCTGATATATA[C/T]GTGCCCAGTTAAGAA | 7347 |
rs775734642 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75603457 | GAATATAAGTGAGGC[C/T]CTGTCTCTAAATTAA | 7347 |
rs775841457 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562781 | CTGTTGAAAGGAAGA[A/G]CACAGTTCTAAAGTA | 7347 |
rs775852972 | snp | A/G | 1.68846e-05 | 0.00290552 | splice-donor-variant | UCHL3 | GRCh38.p7 | 13:75566852 | ACAAGATGCACTTTG[A/G]TAAATGATTTTTCAT | 7347 |
rs775907688 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592329 | TACAAGAATAGTCAT[A/T]CTACATCTATGAAGT | 7347 |
rs775977662 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553345 | GTGTACCATTTCGTA[G/T]TAACTTTTTTTGTCA | 7347 |
rs775987659 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588077 | TTGCCAATACCCATG[A/C]AAAAGTAAGAGGCTA | 7347 |
rs776173957 | snp | C/T | 1.66197e-05 | 0.00288263 | missense, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604774 | TTTTCCACAGATGGG[C/T]GGAAGCCATTTCCAA | 7347 |
rs776289278 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574431 | GTTTGTCTTGTTCGC[G/T]TTGAATCCCCAAGAC | 7347 |
rs776318628 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | UCHL3 | GRCh38.p7 | 13:75594926 | CCAGGCACCAAGTAT[A/G]GATGAGAAAGTAGAT | 7347 |
rs776345156 | snp | A/C | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548191 | CTGAGTCCAGCAGAG[A/C]CTAAGAGTCTGGCAA | 7347 |
rs776356098 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | UCHL3 | GRCh38.p7 | 13:75567320 | ACTATGATGTCGGTA[C/T]CTTCTTTCCGTTTTG | 7347 |
rs776376283 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559923 | TCTCATTTTTTCTCT[A/G]TGTGATAGATTAAGG | 7347 |
rs776438675 | snp | G/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596304 | GAGGAGTAATAAAAC[G/T]TAAATGAGAAGAAGT | 7347 |
rs776444641 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582100 | ATGTGGCTTTGGGCA[A/G]GTCAAGTAGGTCCTT | 7347 |
rs776449826 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549932 | TTGCTGCCGCGAGTC[C/T]ACGGTGGTTTGTCTC | 7347 |
rs776454310 | snp | C/G | | | intron-variant | COMMD6 | GRCh38.p7 | 13:75547102 | ATGTGTATTTTCTCT[C/G]TAAGGCACATGAAAG | 7347 |
rs776509939 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591698 | AATCCAGATTCTACC[A/T]CTTACTAGCTATATG | 7347 |
rs776533367 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561230 | GAGCCACTGTTCCCA[A/G]CCCAATTTCTTTTTC | 7347 |
rs776595411 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75583394 | ATATAAGTTTTTATT[A/G]GAAAACATGATGCTC | 7347 |
rs776748755 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557765 | CAGTTCTATAGATTT[G/T]TAACTTACAGCTACA | 7347 |
rs776763308 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578233 | GTATACTATCATGTG[A/C]GTAAACCACAATTTA | 7347 |
rs776790620 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591178 | TTCCCCTTATTTACC[C/T]TTCTAGTGTTATACT | 7347 |
rs776796797 | snp | C/T | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605233 | ACACTTACGGCCAGG[C/T]GTAGTGGCTCACGGC | 7347 |
rs776829672 | snp | A/G | 8.2618e-05 | 0.00642668 | missense, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605763 | AGAAGTTTATGGAGC[A/G]CGACCCTGATGAACT | 7347 |
rs777027744 | snp | C/T | 0.430604 | 0.172865 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566679 | AAATACACTGTTGAC[C/T]TTTTTTTTTTAATAG | 7347 |
rs777059224 | in-del | -/A | 3.31862e-05 | 0.00407333 | frameshift-variant, nc-transcript-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75604788 | GCGGAAGCCATTTCC[-/A]ATTAACCATGGTGAA | 7347 |
rs777071807 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75599410 | CCTCATTTGACTGTA[A/C]TTTACATATATTTCA | 7347 |
rs777128254 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579496 | TGTTTCTTCTGAACA[G/T]TGCTTGAATAGAGGC | 7347 |
rs777234056 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559031 | CTCAGCCCCGGACTC[-/T]TTTTTTTTTTTTTTT | 7347 |
rs777278783 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591792 | TATATTACGTACCTT[A/G]TTGGGTTTATACAGG | 7347 |
rs777375974 | snp | A/G | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75551148 | TAAAAGAGGGGAGAC[A/G]GCCAGGCGCGGTGGC | 7347 |
rs777406437 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563512 | AAAAATAAATTTTAT[C/T]GTGTATATTTGAAGT | 7347 |
rs777416742 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550722 | CTTATTTTACCCTGT[-/T]TTTTTTTTTTTTTTC | 7347 |
rs777524100 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600166 | AAAGGTCTGAAGCTA[A/G]CAGTTGGTTCATGAG | 7347 |
rs777553216 | in-del | -/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75560083 | GAAGCCAGTAGTTTA[-/C]TTCCTATATCCAGCA | 7347 |
rs777564164 | snp | C/G | | | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75595948 | CCATAAGACCTTCTC[C/G]AGTTTTAAAAAAGCC | 7347 |
rs777593827 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75578975 | AATAGTATAAAGTTT[C/T]ATCTTCATTAGATGT | 7347 |
rs777628805 | snp | A/G | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75598726 | TGCCCCATTACTGGT[A/G]ATGTTTAGTGACTTT | 7347 |
rs777685249 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575301 | GTAGCCCCACCTCAC[A/T]TATGCTTCATTAACT | 7347 |
rs777718670 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586390 | GAGGCAAACACTGTT[A/G]GAACTGAAAAGAGAA | 7347 |
rs777909327 | snp | C/T | 9.89462e-05 | 0.00703302 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605710 | ACTGAAAAATCATAC[C/T]TTTTTTTTTCCTCCA | 7347 |
rs777910997 | in-del | -/GTATATAC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75592429 | CATATATATATATAT[-/GTATATAC]ATATATATATATATA | 7347 |
rs778027013 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75571869 | TATGTATATTATAAC[C/T]CTAAAATGTGTTGGA | 7347 |
rs778053733 | snp | C/G | 5.0229e-05 | 0.00501118 | utr-variant-3-prime, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605863 | TTGCAACTAAATTTT[C/G]TCTGCCATACACTAA | 7347 |
rs778105257 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554810 | TTTGTTATATAGGTA[A/T]ACTCATGTCACAGGG | 7347 |
rs778105647 | snp | C/T | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596019 | AGATACCGTGAGTTT[C/T]GGTTCTATTACCTCT | 7347 |
rs778294546 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584240 | TGCCTCCACAAGCCC[A/G]CCATTAGACTAGCAA | 7347 |
rs778386492 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75570904 | GGGACAGAGCAGGAC[C/T]CTGTCTCTATAAAAT | 7347 |
rs778468100 | snp | A/T | 2.29713e-05 | 0.00338897 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549794 | AAGGCGGCGGCTGTC[A/T]GAGCTGGAGGGCCGG | 7347 |
rs778501332 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564913 | GTTAGCCTGGCTGGT[C/G]TTGAACTCCTGACCT | 7347 |
rs778530727 | snp | A/G | 1.66269e-05 | 0.00288326 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549878 | GTGGGCGCGCTTCGG[A/G]GCAGCCCTGGGCCGT | 7347 |
rs778587420 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | UCHL3 | GRCh38.p7 | 13:75566789 | AGCAAACAATCAGCA[A/G]TGCCTGTGGAACAAT | 7347 |
rs778688416 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75551973 | ATTTATTATAAGTAC[A/G]ATAAGAAAAAGAACA | 7347 |
rs778702953 | snp | C/G | 1.68769e-05 | 0.00290485 | intron-variant | UCHL3 | GRCh38.p7 | 13:75595034 | AGAGAAATGGTAAAT[C/G]GGAAAGTCTCTACTT | 7347 |
rs778758481 | snp | C/T | | | | | GRCh38.p7 | 13:75598888 | AAAAAAAAATTCCCC[C/T]AACATTAGAAGCTTT | 7347 |
rs778765426 | snp | C/T | 1.6492e-05 | 0.00287154 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594903 | AATACCTATTTTTCC[C/T]TCCTATTCCAGGCAC | 7347 |
rs778801920 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572965 | TTTTCTGATCATCTC[A/G]TTTAAGATTCATCTC | 7347 |
rs778835624 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75553001 | CAAAATATTTTCTAG[C/T]GTAATACCGAAAGGG | 7347 |
rs778836073 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600264 | GCTGCAAGTTATCCA[C/G]AAGATCAAGCTCAGA | 7347 |
rs778856290 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75601147 | GCTTCTTAAAGATGA[A/G]CAAATAAACTGATTT | 7347 |
rs778862046 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75574036 | TCCTGGCTAACACAG[C/T]GAAACCCCGTATCTA | 7347 |
rs778887458 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75569995 | CTGGGTTGCTTTTCC[-/T]TTTCCTTCTCTTGCC | 7347 |
rs778925072 | snp | C/G | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549154 | TGTCTTGTCCACTGC[C/G]TCTACTCTACAGTGA | 7347 |
rs778944386 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75588599 | CATATTTTTTAACCC[C/T]GCATCAAAATGATAG | 7347 |
rs778982990 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558043 | CAGAGGTAGTCTTTA[C/T]AGCTGCTTTTATTCT | 7347 |
rs778987966 | in-del | -/GGCGGCGAA | 0.000113186 | 0.00752199 | intron-variant, upstream-variant-2KB, cds-indel | UCHL3, COMMD6 | GRCh38.p7 | 13:75549772 | GGCGGAAGCGGCGGC[-/GGCGGCGAA]GGCGGCGGCTGTCAG | 7347 |
rs779043780 | snp | C/T | 3.34476e-05 | 0.00408934 | utr-variant-5-prime, synonymous-codon | UCHL3 | GRCh38.p7 | 13:75560779 | ATTAGGTCTACATCC[C/T]AACTGGCAATTCGTT | 7347 |
rs779068967 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75591167 | GCATTCTTTCCTTCC[C/T]CTTATTTACCCTTCT | 7347 |
rs779137098 | snp | A/G | 0.000165815 | 0.00910383 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549772 | GGCGGAAGCGGCGGC[A/G]GCGGCGAAGGCGGCG | 7347 |
rs779154779 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589603 | TGCGTTACATGGTTT[G/T]TGTGTGTGTGTTACT | 7347 |
rs779174735 | snp | C/T | | | intron-variant, downstream-variant-500B | UCHL3 | GRCh38.p7 | 13:75601889 | CCGAGGTGGGTGGAT[C/T]ACAAGGTCAGGAGAT | 7347 |
rs779184142 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550006 | AGTGAGGTGTCTGTC[C/G]CTCGGGACCTCGGAG | 7347 |
rs779207609 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572329 | TATTTGCATTTTAGC[C/T]ATTTCATATTCTCTT | 7347 |
rs779277897 | snp | A/G | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605028 | GCTCTATGAACAAAT[A/G]TAAAAATTGAAAAGG | 7347 |
rs779364962 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573585 | ACTGTAGCCTTACCT[G/T]GCCTGTCCTGTGTAT | 7347 |
rs779443132 | snp | A/G | 3.30502e-05 | 0.00406497 | missense | UCHL3 | GRCh38.p7 | 13:75566749 | TCTCAGGGACAAGAT[A/G]TTACATCATCAGTAT | 7347 |
rs779481182 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75555832 | TCCTGGGGTCAAACA[A/G]TTCTGCCACCTCAGC | 7347 |
rs779499197 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557257 | ACCTGCCTTGCCATG[G/T]CAGTAGAGGTGAAGT | 7347 |
rs779522568 | snp | A/T | | | downstream-variant-500B, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75606029 | TTTATCTTGTTTGAA[A/T]ACTAGCAATAGCTTT | 7347 |
rs779548682 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | UCHL3 | GRCh38.p7 | 13:75567267 | CCTGGAGGAATCTGT[A/G]TCAATGAGCCCTGAA | 7347 |
rs779581625 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75580612 | TCAAGTATTCTCACC[G/T]TCTTAATTCTTACTC | 7347 |
rs779613631 | snp | A/C | 1.65165e-05 | 0.00287367 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569435 | TAGGCATTTTTTCCA[A/C]TGAATACCTTTATTC | 7347 |
rs779642636 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75600389 | AGAGAGGAGATGTCA[A/G]CACCTGCCTTCAAAG | 7347 |
rs780000394 | in-del | -/TTTATGTATGTATGTA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75563125 | GGTACCTCATTATCC[-/TTTATGTATGTATGTA]TTTATGTATGTATGT | 7347 |
rs780005105 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561162 | CTGGTCTCCAACTCG[G/T]GCTCAAGTGATCCTC | 7347 |
rs780012825 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75575550 | TTTAATTCCAGTACC[A/G]GCCCTATGAGGTATT | 7347 |
rs780057533 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549996 | CAACCAGGTGAGTGA[C/G]GTGTCTGTCGCTCGG | 7347 |
rs780103496 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576306 | GCAATCTCTGCTCAC[A/T]GCAACGTCTGCCTCC | 7347 |
rs780107941 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584771 | TATTAACATAAGAAA[A/G]AATCAAATGGAAATG | 7347 |
rs780256969 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573803 | GTATGAATTTGGCAG[A/G]GGGGACACAATTCAG | 7347 |
rs780294833 | snp | A/G | 1.67671e-05 | 0.00289539 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75549867 | CCAATCCCGAGGTGG[A/G]CGCGCTTCGGGGCAG | 7347 |
rs780306938 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | UCHL3 | GRCh38.p7 | 13:75594880 | TTTGTTTGACTACTA[A/G]TGTATATAATACCTA | 7347 |
rs780313144 | in-del | -/TCTGTCGCTCGGGACCTCGGAGTCTTT | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550000 | CAGGTGAGTGAGGTG[-/TCTGTCGCTCGGGACCTCGGAGTCTTT]TCTGTCTGCTCGGTC | 7347 |
rs780333734 | in-del | -/A | | | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605509 | GCAAGACTCTGTCTC[-/A]AAAAAACAAACAAAC | 7347 |
rs780345235 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558824 | CATTGAATAAGACAC[A/G]GTTTTTTCCCTTGAC | 7347 |
rs780531088 | in-del | -/CTCCCACCTCAGC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75564258 | TGGGTTCGCGCCATT[-/CTCCCACCTCAGC]CTCCCGAGTAGCTGG | 7347 |
rs780566100 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594661 | TCTAAGGTGAACACA[A/G]TTTTTGGTCTTTAGA | 7347 |
rs780656144 | snp | A/T | 1.75207e-05 | 0.00295973 | intron-variant | UCHL3 | GRCh38.p7 | 13:75566900 | CTTAAGATACAAGTT[A/T]ATTGCATTGAGCAGT | 7347 |
rs780661979 | snp | C/G/T | | | intron-variant, missense | UCHL3 | GRCh38.p7 | 13:75590100 | TGGCGACCCTTCTTA[C/G/T]GTCTACCATCTTTGG | 7347 |
rs780690932 | snp | C/T | 1.66156e-05 | 0.00288228 | intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605721 | ATACTTTTTTTTTTC[C/T]TCCATAGGATGCCAT | 7347 |
rs780731674 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75568269 | TTGGTTAGAACAATG[C/T]CTTATGTAGAATTTG | 7347 |
rs780762320 | snp | A/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75589057 | ATTTCTCTCCTTAAC[A/T]GTATGTGTCCCATGT | 7347 |
rs780817839 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75554617 | TTCTTCTGCTTCTCC[G/T]TTTGCTTCCCTAAAA | 7347 |
rs780868018 | snp | A/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577004 | CCAGTAATGCCAGCA[A/C]TTTGGGAGGCCAAGA | 7347 |
rs780882142 | in-del | -/GTATACGTATACATACGTATACGTATATACGTACGTATATAC | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561797 | TGTGTGTGTATATAT[lengthTooLong]GTATACGTATACATA | 7347 |
rs780896261 | in-del | -/TTT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75557962 | AGGACATTTTAATGA[-/TTT]TTTTTTTTTTTGAAG | 7347 |
rs780980995 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon, intron-variant | UCHL3, LMO7-AS1 | GRCh38.p7 | 13:75605809 | TGCTCTTTCTGCAGC[A/G]TAGCTTGTCAATAAT | 7347 |
rs781089163 | snp | G/T | 2.1329e-05 | 0.00326559 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | UCHL3, COMMD6 | GRCh38.p7 | 13:75549801 | CGGCTGTCAGAGCTG[G/T]AGGGCCGGGCACCGC | 7347 |
rs781097642 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75577313 | GAATATATACAGACT[C/T]TTTTCTTGTCATTAT | 7347 |
rs781100669 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75576388 | GCACGTGCCACCACA[C/T]CCGGCTAATTTTTTG | 7347 |
rs781116275 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75549213 | GTGATTTCTAGTACT[C/T]GACATTTTTTGTCAA | 7347 |
rs781153520 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75597311 | CTACAGTGTGCTATG[A/G]TTGCACCTGTGAACA | 7347 |
rs781187352 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75562083 | ATGATTTGTCATATT[C/T]GTGCTCAGGTCATCC | 7347 |
rs781217157 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75572636 | TAACCAGAATTAGCT[C/T]AGAACTGTCCTTGGT | 7347 |
rs781258928 | snp | C/T | 1.66729e-05 | 0.00288724 | utr-variant-5-prime, missense | UCHL3 | GRCh38.p7 | 13:75560799 | GGCAATTCGTTGATG[C/T]ATATGGAATGGATCC | 7347 |
rs781296965 | snp | C/T | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550042 | TCTGTCTGCTCGGTC[C/T]GCTTCCCTGCTGGAC | 7347 |
rs781315665 | snp | G/T | 1.8696e-05 | 0.00305739 | intron-variant | UCHL3 | GRCh38.p7 | 13:75560907 | TGTAAAATAGAAAGT[G/T]TCTGGTAAATACAAT | 7347 |
rs781324510 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75559132 | GCAAGCTCCGCCTCC[C/T]GGGTTCATGCCATTC | 7347 |
rs781329408 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75565543 | GGGGATCAGGAAAAT[G/T]TTTCTGTAAAGGACT | 7347 |
rs781342676 | snp | C/G | 1.69066e-05 | 0.00290741 | intron-variant, upstream-variant-2KB, synonymous-codon | UCHL3, COMMD6 | GRCh38.p7 | 13:75549859 | GCTGGAGGCCAATCC[C/G]GAGGTGGGCGCGCTT | 7347 |
rs781445517 | snp | A/G | 5.20251e-05 | 0.00509998 | intron-variant | UCHL3 | GRCh38.p7 | 13:75569552 | GCTATAAATTTAACC[A/G]TATAAATTTCTTGCT | 7347 |
rs781516708 | snp | A/T | | | utr-variant-5-prime, missense | UCHL3 | GRCh38.p7 | 13:75560775 | AACAATTAGGTCTAC[A/T]TCCTAACTGGCAATT | 7347 |
rs781555331 | snp | C/G | 3.30715e-05 | 0.00406628 | missense | UCHL3 | GRCh38.p7 | 13:75566815 | ACAATTGGACTGATT[C/G]ATGCTATTGCAAACA | 7347 |
rs781675453 | in-del | -/AT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561543 | TACAGTTTTTTCAAT[-/AT]ATATATATATATAAG | 7347 |
rs781689840 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75594789 | TATACCAAACATTAA[A/G]CCTTGAATTATATTG | 7347 |
rs781749801 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75582871 | TTACGTTTCCATAAT[A/G]GCACACTTTATTTCA | 7347 |
rs781752275 | snp | G/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75584500 | TAAACTCTTGACTAG[G/T]TTGGCTTATCCCCAT | 7347 |
rs796130147 | snp | C/T | | | upstream-variant-2KB, intron-variant | UCHL3, COMMD6 | GRCh38.p7 | 13:75548355 | TCTGAAGTCAAAGAA[C/T]AGTGGCCAGAAGAAC | 7347 |
rs796152821 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595631 | AAAAAAAAAAAAGAG[C/G]GTAATAGTTGTAATG | 7347 |
rs796159692 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573674 | CTTCCTGTTCTTATA[A/G]GGATACCAGTCCTGT | 7347 |
rs796225130 | snp | C/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75585393 | GCAAGCCAGAACACA[C/T]AGAATGATATTTTTA | 7347 |
rs796231083 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75566689 | TTGACTTTTTTTTTT[-/T]AATAGTATGAAGTAT | 7347 |
rs796237427 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75579716 | TAGATGAAACTCGTC[-/T]TAAGAATGCTTTCAG | 7347 |
rs796242160 | snp | C/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595572 | ATGGTACTCCAGCCG[C/G]GGCAACAGGAGTGAT | 7347 |
rs796272566 | in-del | -/A | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75586094 | GTTTAGTAAAAAAGC[-/A]AAGACACAATTATAT | 7347 |
rs796321844 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75595598 | GTGATACTCCATCTC[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 7347 |
rs796389074 | in-del | -/AT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75561542 | AATACAGTTTTTTCA[-/AT]ATATATATATATAAG | 7347 |
rs796422662 | snp | A/G | | | intron-variant, utr-variant-3-prime | UCHL3 | GRCh38.p7 | 13:75596730 | TTATCTTAAAAAAAA[A/G]CTCGGTTTTACTAGT | 7347 |
rs796429458 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581363 | TTTTTTTTTTTTTTT[-/T]CCTTGAGACAGGGTC | 7347 |
rs796526571 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550735 | GTTTTTTTTTTTTTT[-/TT]CATTCTCAACAGCTC | 7347 |
rs796574735 | snp | A/G | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75558689 | TTCACTGATGTATAT[A/G]GACATACAGATGGCT | 7347 |
rs796618373 | in-del | -/AT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75552032 | AATGTAATACATGGA[-/AT]AGTGACAGGAGACCT | 7347 |
rs796734204 | in-del | -/TT | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75590178 | GTGACAAGGGCTGTC[-/TT]TTTTTTTTTTTTTTC | 7347 |
rs796938473 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | UCHL3, COMMD6 | GRCh38.p7 | 13:75550721 | CCTTATTTTACCCTG[-/TTT]TTTTTTTTTTTTTCA | 7347 |
rs796962917 | in-del | -/T | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75581710 | TTTTTTTTTTTTTTT[-/T]AAGTCTGGATCATTT | 7347 |
rs796984280 | in-del | AA/C | | | intron-variant | UCHL3 | GRCh38.p7 | 13:75573272 | CTGTCTCAGAAAAAA[AA/C]AAAAAAAAAAGATTC | 7347 |