SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2705 | snp | C/T | 0.48978 | 0.0707512 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445076 | AACGGCAGGAGGGGA[C/T]GCTGGCCTTCCTGCA | 80700 |
rs11909 | snp | C/T | 0.47109 | 0.116702 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454003 | GATGGCAGCCGCTGC[C/T]GCCCTAGCCCGGCTG | 80700 |
rs243385 | snp | G/T | 0.445064 | 0.156365 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444953 | CAAGCCATCCGCTCT[G/T]CAGCAGGTGGGCCTG | 80700 |
rs243387 | snp | C/T | 0.489722 | 0.0709447 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445159 | CTGCAGCATGGGTCC[C/T]GTTCCCGTGTGCCGT | 80700 |
rs243388 | snp | A/G | 0.0230416 | 0.104839 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446435 | CCCCGGCCAGCCCTC[A/G]TGACCTGGCCCGCGT | 80700 |
rs243389 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446998 | CAATAGCGAGAGCCG[A/G]GCCCCTGGACTGGGT | 80700 |
rs243390 | snp | A/G | 0.489201 | 0.0726845 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449255 | TGTTCACCCGCCCTC[A/G]TCTGGGCAGCCCAGG | 80700 |
rs243391 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449811 | TAGATCTTGGCTCAG[C/T]TTTCTTCTCAGCCCC | 80700 |
rs243392 | snp | C/T | 0.488302 | 0.0755777 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450182 | gctggagtgcagtgg[C/T]gcaatctcagctcac | 80700 |
rs243393 | snp | A/G | 0.482757 | 0.0912364 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450745 | ttgagacagagtctc[A/G]ctctgtcgcccaggc | 80700 |
rs243394 | snp | A/T | 0.48155 | 0.0942576 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451563 | acttcggctttagcc[A/T]gggcaacatggcaaa | 80700 |
rs243395 | snp | C/T | 0.464033 | 0.12919 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452500 | CTTGGACGCTTTCAC[C/T]GCCCCAGGTATCTGA | 80700 |
rs243396 | snp | A/G | 0.480697 | 0.0963277 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453232 | GGGCCTCAGGTACAC[A/G]AGCCCATCGCTCCCT | 80700 |
rs243397 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454830 | CTCCCAGCAGGGTCC[C/T]GGCACACAGTAGGTG | 80700 |
rs376965 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453327 | CCTTGCAAGGTGGAC[A/G]CAGGTTGTGGTGGAA | 80700 |
rs411833 | snp | C/G | 0.488905 | 0.0736498 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453328 | TCCACCACAACCTGT[C/G]TCCACCTTGCAAGGC | 80700 |
rs741923 | snp | A/G | 0.422315 | 0.181128 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448846 | TCTGGAACCACTCCC[A/G]GGCCTCATGTTTACA | 80700 |
rs760369 | snp | C/T | 0.282632 | 0.247861 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449290 | GGCAGCCCAGGGCCA[C/T]GTGTCAGGATTCGGG | 80700 |
rs1044477 | snp | A/G | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445083 | GGGTGACAACGGCAG[A/G]AGGGGATGCTGGCCT | 80700 |
rs1044510 | snp | A/G | 0.460898 | 0.134246 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457653 | CGACATCAAGTTCAA[A/G]AGCGCGGGACCCGGT | 80700 |
rs1127888 | snp | A/G | 0.344869 | 0.2313 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454086 | GTTCCCAGGGAAAAG[A/G]CCCACAAAGAGAAGC | 80700 |
rs2077444 | snp | A/G | 0.424037 | 0.179474 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449413 | CATGAGCCCCGGCTC[A/G]GTGTGTAGGTCATTG | 80700 |
rs2272639 | snp | C/T | | | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447614 | GGGTGCAGGTGGATG[C/T]TGTCCAGGTACCTGG | 80700 |
rs2293930 | snp | C/T | 0.422473 | 0.180978 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444859 | AGGTGGGTGGCTCAT[C/T]GGGCACTTGTGGCCA | 80700 |
rs3830686 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445205 | AGGGAGATGCCACGT[-/T]GTGTCTGTCCGGCAG | 80700 |
rs4806983 | snp | A/G | 0.111928 | 0.208413 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459782 | caggaggcagagctt[A/G]cagtgagccgagatc | 80700 |
rs4807589 | snp | A/G | 0.105569 | 0.204058 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444686 | GCCAGGTGAAGTTGC[A/G]CATCTGCAGGTTCCA | 80700 |
rs6510808 | snp | A/T | 0.488485 | 0.0749998 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458914 | ACCCAATGCACCCAA[A/T]TGGGACCTGGGGATT | 80700 |
rs7253478 | snp | A/G | 0.482008 | 0.0931261 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456190 | CCCTGCATCCTTCCT[A/G]TCATGCCCAGTCCCA | 80700 |
rs7257129 | snp | C/T | 0.482008 | 0.0931261 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456385 | CCCACTGCCCCGTGA[C/T]TCCTGACCCCCACTT | 80700 |
rs8101961 | snp | A/G | 5.11967e-05 | 0.00505922 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446632 | GCGCGCACGGGCTCC[A/G]CAGCCAGCAGCTGTT | 80700 |
rs8110072 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448703 | TGACGCGACAGAACT[G/T]TGCCTCACACTCTGG | 80700 |
rs10423797 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457461 | CCTCGGCCCGACTTC[C/G]TCCGCCCCCGGCGCC | 80700 |
rs10423822 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457500 | TCCCCTGACCCTCGC[C/G]TGCCGCTCCCAGCCC | 80700 |
rs10425294 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457460 | CCCTCGGCCCGACTT[C/G]GTCCGCCCCCGGCGC | 80700 |
rs10425328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457499 | CTCCCCTGACCCTCG[C/G]GTGCCGCTCCCAGCC | 80700 |
rs10432304 | snp | A/T | 0.459233 | 0.136827 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458245 | CTCTATAAAAAAAAA[A/T]AAAATAAAATAAAAT | 80700 |
rs11085075 | snp | A/G | 0.482683 | 0.0914256 | upstream-variant-2KB, missense | UBXN6 | GRCh38.p7 | 19:4457847 | GCCGCCGGAAGTCCC[A/G]CCTTCCCCTGGCCTG | 80700 |
rs11558242 | snp | C/G/T | 0.000107549 | 0.0073324 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453494 | TCAAGCCGAAGCCAC[C/G/T]GTCAGCGGGAGCCCC | 80700 |
rs11670503 | snp | A/G | 0.259951 | 0.249802 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458066 | GACAGGGACAGGCCA[A/G]CTGAACCTCGCAGAG | 80700 |
rs12459922 | snp | A/G | 0.27893 | 0.24832 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455865 | TTCCCAAACCACCTG[A/G]CGGCCCCTGCTCACC | 80700 |
rs12608655 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458556 | TCACCACGTACCCTA[A/G]GTAGGAGCTGTTTAA | 80700 |
rs12609703 | snp | C/T | 0.48692 | 0.0798058 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456156 | CAGGCTCTGGGCTGA[C/T]CCAGCCATCACCCCG | 80700 |
rs12977256 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[A/T]AAAAAAAAAAAAAAA | 80700 |
rs12985005 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457726 | ccggcggcggggggc[C/T]gcgggggcggggggg | 80700 |
rs12985963 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457799 | CGGAAGAAAATTaaa[A/T]aaaaaaaaaaaaaaa | 80700 |
rs34179017 | snp | C/T | 0.00404235 | 0.0447754 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446167 | GGGAGCGGCTGGGGG[C/T]GGTGTACGGGTTCGT | 80700 |
rs34822893 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445778 | CCTCCTGCCCTCTCC[C/T]TCCGGGACTCCAGGA | 80700 |
rs35081974 | in-del | -/C | | | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448255 | GGGGGTGACAGCCCC[-/C]AGTGGGAGGGGTGCT | 80700 |
rs35111635 | in-del | -/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444750 | CCTCTGGCCACAGGG[-/G]AAGCCAGGCCTGTGA | 80700 |
rs35137279 | snp | A/G | 0.0452528 | 0.143452 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459654 | CATCCCGGCTAATAC[A/G]GTGAAACCCTGTCTT | 80700 |
rs35208178 | multinucleotide-polymorphism | CG/GC | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457460 | CCCTCGGCCCGACTT[CG/GC]TCCGCCCCCGGCGCC | 80700 |
rs35436704 | snp | C/T | 0.0145626 | 0.0840787 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445550 | CCGCGGGGGCCGAGC[C/T]GGACTCCATCCTGAA | 80700 |
rs35539786 | multinucleotide-polymorphism | CG/GC | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457499 | CTCCCCTGACCCTCG[CG/GC]TGCCGCTCCCAGCCC | 80700 |
rs35708976 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455476 | AGGGCACCTCACCCC[-/C]AACCAGCCATGGACC | 80700 |
rs45464495 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455465 | ATGCCATTTCCCAGG[A/G]CACCTCACCCCAACC | 80700 |
rs45503199 | snp | C/T | 0.0548986 | 0.156324 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446243 | GCCCAGGGCCCCCTA[C/T]CAACCCGAGCCGCCC | 80700 |
rs55661974 | snp | C/G | 0.438386 | 0.164349 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459150 | GCCAACATGGTGAAA[C/G]CCTGTCTCTATGGGC | 80700 |
rs55674497 | snp | A/G | 0.421526 | 0.181876 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459218 | GAATCGCTTGAACCC[A/G]GCAGGTGGAGGTTGC | 80700 |
rs55940498 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451970 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 80700 |
rs56153949 | snp | C/G | 0.251578 | 0.249995 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457521 | CTCCCAGCCCCTCAT[C/G]CTCTCCGATCTCCCG | 80700 |
rs56156435 | in-del | -/GCC | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444659 | CCTTTCATCATACCC[-/GCC]AAGCCCCTCTTGCCA | 80700 |
rs56254866 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457801 | GAAGAAAATTAAAAA[A/T]AAAAAAAAAAAAAAA | 80700 |
rs57787685 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457802 | AAGAAAATTAAAAAA[A/T]AAAAAAAAAAAAAAA | 80700 |
rs58895127 | in-del | -/TAA | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[-/TAA]AAAAAAAAAAAAAAA | 80700 |
rs58900477 | in-del | -/AAA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450786 | AAAAAAAAAAAAAAA[-/AAA]GAGTGCCTACAAATC | 80700 |
rs59106361 | snp | C/G | 0.0562307 | 0.157967 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448185 | TGGGTGGAGCTGCCT[C/G]ACTCTCGGCCTATGC | 80700 |
rs59121637 | snp | A/G | 0.175897 | 0.238765 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452186 | AGTTGGGAGAGAGGA[A/G]ATACAGATGCATACA | 80700 |
rs59258359 | snp | C/T | 0.02016 | 0.0983543 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445368 | CAGCTCCACGGCTGG[C/T]GCCCCTCCCGTGCCC | 80700 |
rs60079641 | snp | C/G | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457193 | AGAGCTCTCCCTCAC[C/G]ACCCGGCTCAGGACT | 80700 |
rs60087438 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448488 | CGCTGCCCAGGTAAC[-/AG]GGGCAGGAAAAGGAA | 80700 |
rs60981683 | snp | C/T | 0.0433974 | 0.140767 | upstream-variant-2KB, missense | UBXN6 | GRCh38.p7 | 19:4457925 | CTGGCCCAGGGCGGC[C/T]GCTCTGTACGCTGGA | 80700 |
rs61729794 | snp | A/G/T | 0.000231089 | 0.010747 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445555 | GATGGAGTCCGGCTC[A/G/T]GCCCCCGCGGCCTTG | 80700 |
rs62130982 | snp | A/G | 0.0596104 | 0.162024 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448483 | CCCTCCGCTGCCCAG[A/G]TAACAGGGGCAGGAA | 80700 |
rs62130983 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450094 | CCCGGGTGTGGTGGC[C/G]TGCACCTGTAGTCCC | 80700 |
rs62130984 | snp | C/T | 0.423413 | 0.180077 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450328 | CCAAAAGCCATGAAC[C/T]AAAACTGACACATTT | 80700 |
rs62130985 | snp | A/C | 0.422944 | 0.180528 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450333 | AGCCATGAACTAAAA[A/C]TGACACATTTAATTA | 80700 |
rs62130993 | snp | C/T | 0.438386 | 0.164349 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459153 | AACATGGTGAAAGCC[C/T]GTCTCTATGGGCACC | 80700 |
rs67614381 | in-del | -/T | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450786 | GATTTGTAGGCACTC[-/T]TTTTTTTTTTTTTTT | 80700 |
rs70947751 | multinucleotide-polymorphism | CC/TG | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453327 | TTCCACCACAACCTG[CC/TG]TCCACCTTGCAAGGC | 80700 |
rs71166999 | in-del | -/TT | 0 | 0 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458889 | ATTGGGTGCATCCTC[-/TT]TTTTTTTTTTTTTTT | 80700 |
rs72990638 | snp | C/T | 0.423257 | 0.180228 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453238 | CGATGGGCTCGTGTA[C/T]CTGAGGCCCACTTCT | 80700 |
rs72990643 | snp | C/T | 0.273856 | 0.248859 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454739 | CAGGAATTGAGGAGA[C/T]TCAAGGGGTGTCACA | 80700 |
rs72990646 | snp | A/C | 0.0252325 | 0.109451 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458519 | GGCCTGTTTTGGTGC[A/C]TGAAGCACCCCCCCG | 80700 |
rs73541319 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448228 | CACCTCAGCAGGTAA[C/T]GAGGGGGCCAGAGGG | 80700 |
rs74788480 | snp | C/T | 0.000137611 | 0.00829376 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446060 | TCACCAGCCCGCACT[C/T]GTTCAAGGCCAGGTT | 80700 |
rs74938087 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445308 | GCTTGGGCGCATCCC[A/C]ACAGCCCCCAAGGGA | 80700 |
rs74995992 | snp | C/G | 0.0333695 | 0.124785 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445286 | TCCCCAGGCCTCTCC[C/G]TCGGGGGCTTGGGCG | 80700 |
rs75122921 | snp | A/C | | | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446164 | CGGACGAACCCGTAC[A/C]CCGCCCCCAGCCGCT | 80700 |
rs75475637 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447058 | CAGCCCTGGGGGTGC[C/T]TCAGTGCTGGATGCA | 80700 |
rs75762432 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458244 | TCTCTATAAAAAAAA[A/T]AAAAATAAAATAAAA | 80700 |
rs77077573 | snp | A/G | 0.000577639 | 0.0169849 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445562 | TCCGGCTCGGCCCCC[A/G]CGGCCTTGATGTCCT | 80700 |
rs77324462 | snp | A/C | 0.5 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450221 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 80700 |
rs77562484 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448693 | GAAGCCAGTGTGACG[C/T]GACAGAACTGTGCCT | 80700 |
rs77571267 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444962 | CGCTCTTCAGCAGGT[A/G]GGCCTGCCCTGTGTC | 80700 |
rs77767396 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450992 | GGGACACGGGTGCTT[C/T]TGCACACACTGCTGG | 80700 |
rs78035520 | snp | A/C/T | 0.000115848 | 0.00761005 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446848 | TACCCTGATCCTGGG[A/C/T]GGGAAGCAACACCTT | 80700 |
rs78869060 | snp | A/G | 0.277067 | 0.24853 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444745 | CCTGTCCCTCTGGCC[A/G]CAGGGAAGCCAGGCC | 80700 |
rs79412879 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448994 | GCCCCTGCCCCTCCC[C/T]GAGGTCCCACCTATC | 80700 |
rs79703899 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452298 | TACCACCTGGGCTTC[C/T]GATGGAGGGTGGCTC | 80700 |