SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7958 | snp | A/G | 0.452965 | 0.145963 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451294 | GATGAACAGTATTTC[A/G]TGTGTGCTATGTAGT | 137886 |
rs11752 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451079 | TTAAAAGAATTGAAC[A/G/T]TTGTAAATCAAAGGG | 137886 |
rs726012 | snp | A/G | 0.281313 | 0.248031 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429796 | ACATGGAGACTTCCA[A/G]GGTAAGATGACAATC | 137886 |
rs1001706 | snp | C/T | 0.274661 | 0.248781 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427355 | gtagtcccaactgct[C/T]gggaggctgaggtgg | 137886 |
rs1052499 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434927 | TTAATGTGGCATTAC[A/T]GCTGGCAGAAGATTT | 137886 |
rs1057067 | snp | C/T | 0.386884 | 0.209196 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450065 | gtgtgtgacctgata[C/T]tcagaccttttgatg | 137886 |
rs1060966 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443531 | ggcacagtggctcac[A/G]cctgtaatcccagca | 137886 |
rs1469338 | snp | A/G | 0.264906 | 0.249555 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444897 | ACTTCCATTCAAAAA[A/G]CTTCTCTCTCAGAGT | 137886 |
rs1471104 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444610 | AAATCCAAGAGAAAA[A/G]ACATGAGACACTGAA | 137886 |
rs1529367 | snp | G/T | 0.398354 | 0.201224 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427544 | TACAATGAACACCTT[G/T]AAAATATCCTGCATT | 137886 |
rs1529368 | snp | C/T | 0.366266 | 0.221319 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427366 | AAGCTATCCTGCCAC[C/T]TCAGCCTCCCGAGCA | 137886 |
rs1988172 | snp | A/G | 0.127944 | 0.218179 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422687 | TTTCCCAAGTCTGGG[A/G]GTGCCCCAGTGGGGT | 137886 |
rs1993453 | snp | A/G | 0.39979 | 0.200158 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434625 | GAATATATTAAATAA[A/G]TGGTTGCTGGGGGTG | 137886 |
rs2016886 | snp | C/T | 0.365853 | 0.221536 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415171 | TGTCATTGGGGGTAT[C/T]ACGTGCTATGAGTAT | 137886 |
rs2033142 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424668 | TGTACTCCAACTCCA[C/T]GCTGTGCAGAAATGA | 137886 |
rs2081688 | snp | A/C | 0.387074 | 0.209071 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438595 | GTAAACATTCCCATT[A/C]CAAAAGAGAGATCTG | 137886 |
rs2081689 | snp | C/T | 0.453697 | 0.14494 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438468 | CATATACAGGGCATA[C/T]TGGTGCAAGAGGTGG | 137886 |
rs2162460 | snp | G/T | 0.127944 | 0.218179 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419222 | TAGAAGATATCATAC[G/T]TAGAAAAAAAGATTG | 137886 |
rs2288313 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434601 | TATATTCCAGGAACT[A/G]CTTCTTGAAAACCCG | 137886 |
rs2326075 | snp | C/T | 0.38286 | 0.211774 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413167 | TTCCACCCTAAGTTA[C/T]GATGGGGATTTTTTT | 137886 |
rs2326076 | snp | G/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446259 | TGAAATATGTGGTAT[G/T]TAAACAGTCTCTATA | 137886 |
rs2859998 | snp | A/G | 0.451359 | 0.148171 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411603 | GGGATAGAATCCGGC[A/G]CCCGGTCTCCCGATG | 137886 |
rs3080297 | in-del | -/AT/T/TT | 0.58495 | 0.107276 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434369 | tatatatatatatat[-/AT/T/TT]tTTTTTTTTTTCTAT | 137886 |
rs3857966 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410760 | TATATATGTGTGTGT[A/G]TATATATATATATAT | 137886 |
rs4599797 | snp | A/C | 0.271702 | 0.249056 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449319 | CCCACCCCCCGCTCC[A/C]CTCCTGTGTTAAAGA | 137886 |
rs5891685 | in-del | -/TTTA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446258 | ATGAAATATGTGGTA[-/TTTA]AACAGTCTCTATAAA | 137886 |
rs6982486 | snp | A/G | 0.399073 | 0.200692 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420135 | GCTTTGACTCAAGAT[A/G]GATACATCTCAGTTG | 137886 |
rs6993992 | snp | C/T | 0.453697 | 0.14494 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436494 | cccctacctcgacac[C/T]gaatgacagcagTGC | 137886 |
rs6997864 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447301 | ATATAAAGATTAAAA[A/T]TTTGTGATTTTTATT | 137886 |
rs7006025 | snp | A/G | 0.281577 | 0.247998 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442494 | AAATGAAAATAATCT[A/G]TTGTCTTCCATAGAT | 137886 |
rs7007181 | snp | C/T | 0.363359 | 0.222822 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426720 | TCCGTGACAGACCCG[C/T]TCCTTGCTCAGGCTC | 137886 |
rs7010273 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446137 | TATCTAAGTAGAACT[C/G]TATGTGACTTGAGTA | 137886 |
rs7012712 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427886 | AGGATATGGGCATAT[G/T]TATGTAAGAGGAGGA | 137886 |
rs7813734 | snp | C/T | 0.0599851 | 0.162463 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451712 | CAGGTGCTTCTTTTT[C/T]GCCACAATGGATTTC | 137886 |
rs7817066 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425958 | TCTGGCTCTCTCATA[A/C]AAGAAAACTACCATG | 137886 |
rs7822723 | snp | G/T | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427327 | AAATAGCCAAGCGTG[G/T]TGGTGCACGCCTGTA | 137886 |
rs7823397 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442978 | ACTTCAAAGCCTTAC[C/T]TTATCTCAGCTCCTC | 137886 |
rs7823985 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446865 | tgcagtggcggaatc[G/T]cagcccactacaaac | 137886 |
rs7826302 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410790 | tatatatatatatat[A/T]tttttttttttagta | 137886 |
rs7827559 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446920 | ctcatgctcagcctc[C/T]tgagtagctgggatt | 137886 |
rs7829017 | snp | C/T | 0.449599 | 0.150533 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414276 | CCAGAGTGTGATTCA[C/T]TGGTTCTAGAGTAGA | 137886 |
rs7830535 | snp | A/G | 0.281313 | 0.248031 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441184 | GTTTTGTAGAGACAC[A/G]TGTCTTACTATGTTG | 137886 |
rs7835967 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442726 | GCTAGAGTAGTGCCT[A/G]ACAAAATCACAGAGT | 137886 |
rs7836166 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442596 | GCAAACCAAAATGCT[A/G]TAAAAATGTTACATA | 137886 |
rs7836229 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442828 | AATCATGATTTGAAG[C/T]TGATGTTTCTGCAGA | 137886 |
rs7836301 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442692 | AAACTGTATTATTGA[A/G]TAAAAATTAGCTTGG | 137886 |
rs7839859 | snp | C/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442951 | TAGACCCTGAGGGCT[C/G]TCTTCTCTAAAACTT | 137886 |
rs7839907 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443131 | GCTGctttcctaaac[A/C]ccctcctcgacccct | 137886 |
rs7840036 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446748 | CATATGCTGCTAACA[C/T]ATTTTATACTCCGAA | 137886 |
rs7840636 | snp | A/C | 0.147991 | 0.228242 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443637 | ATCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA | 137886 |
rs7843633 | snp | A/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446983 | ttctggttttagtag[A/T]gacggggttttcacc | 137886 |
rs7844732 | snp | C/G | 0.382085 | 0.212258 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414041 | GGGAGGGAGTGGGAA[C/G]AGGGATAACTTCAGT | 137886 |
rs10095270 | snp | C/T | 0.264906 | 0.249555 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440339 | TTGCAGCAGGAGCAA[C/T]GTGCTTAGCTTTGTG | 137886 |
rs10108817 | snp | C/T | 0.269267 | 0.249256 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431590 | ataaatgctcagaag[C/T]gcaattggtagatca | 137886 |
rs10110824 | snp | C/G | 0.271162 | 0.249103 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423210 | TTGAGCTCTTGGGAG[C/G]TCTGAGCTTCATGTC | 137886 |
rs10111761 | snp | C/T | 0.26518 | 0.249539 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437763 | agagcccgttgaagt[C/T]tggaaaattctcatc | 137886 |
rs10504254 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421589 | ATTACTGACTGGGCT[C/T]TCTCATTACTGGCCC | 137886 |
rs10957054 | snp | C/T | 0.363776 | 0.222609 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423997 | TTTTCTATGACTCTT[C/T]AATGCCAATGCAAAG | 137886 |
rs11552203 | snp | A/G | 0.228842 | 0.249103 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450546 | CCTTTCTTCAAGGCC[A/G]CCCTAGCATTAACAT | 137886 |
rs11988442 | snp | A/C | 0.281049 | 0.248064 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426104 | CCATTCTTCTCTTTT[A/C]ATTGCCCGTGATGTT | 137886 |
rs11989326 | snp | C/T | 0.281049 | 0.248064 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430723 | ATTTTACCTCCTCTT[C/T]CATTTTTCTATTATT | 137886 |
rs11995825 | snp | C/T | 0.287606 | 0.247155 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420978 | TCCCCCAACAACATA[C/T]AGAAAATAAAAACTG | 137886 |
rs11996829 | snp | G/T | 0.398894 | 0.200825 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418723 | CTTTGTAATCAGCAG[G/T]TTGGTATCTTGACAC | 137886 |
rs12543440 | snp | A/G | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420837 | AAGATACAATAAACT[A/G]TATTTTGGAACTTTT | 137886 |
rs12543860 | snp | A/G | 0.453818 | 0.144769 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433386 | ACCAATGATGTGTGA[A/G]TTTTCAGTCTCGATC | 137886 |
rs12545520 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437330 | tttcttttttttttt[C/T]ttttttttttttttt | 137886 |
rs12546328 | snp | C/T | 0.453087 | 0.145793 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442117 | AGAGTTTCCACTTTG[C/T]AGTGCTTACTTCCAC | 137886 |
rs12547722 | snp | A/C | 0.387453 | 0.208822 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437201 | ttgggaactggagta[A/C]aggtcagccttgtta | 137886 |
rs12676903 | snp | C/T | 0.453818 | 0.144769 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445478 | AAGGACTTACTGGTA[C/T]AATATACCTTCATAA | 137886 |
rs12681594 | snp | C/T | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418657 | TAGTGATATGTTCAT[C/T]TGGTTAAGGTGCTGA | 137886 |
rs13252159 | snp | C/G | 0.287346 | 0.247195 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424692 | GAGTACAAGGCGGGG[C/G]GGGGGGCTCTGATCT | 137886 |
rs13253288 | snp | C/G | 0.399253 | 0.200558 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426297 | CTGTAAGCTCCGCCT[C/G]CTGGGTTCATGCCAT | 137886 |
rs13253349 | snp | A/G | 0.451109 | 0.148509 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411926 | GGTTCCATTTTATCA[A/G]GTAGGTTTTTCTTTT | 137886 |
rs13260971 | snp | C/T | 0.234109 | 0.249494 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409883 | ctttatacatcaaaa[C/T]gatcagtatgccaaa | 137886 |
rs13263105 | snp | C/G | 0.399611 | 0.200291 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413036 | AGTGAGAACAGCTTG[C/G]TTAATGACCACCTGA | 137886 |
rs13265462 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446780 | AAAGTACAACCTGCA[A/T]TTTTTtttttttttt | 137886 |
rs13271316 | snp | C/G | 0.278664 | 0.248351 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419430 | TTTCATTATCTGAAA[C/G]TCTGGACATAAGATG | 137886 |
rs13277110 | snp | A/G | 0.271702 | 0.249056 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423687 | tgatccgccagcctc[A/G]gcctcccaaagtgct | 137886 |
rs13277646 | snp | A/G | 0.414862 | 0.187938 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416879 | ATTGTATGAAGATGA[A/G]GTGAAGTGCAAATCT | 137886 |
rs13277801 | snp | C/T | 0.39979 | 0.200158 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440975 | TCGTCTCTCTTTACA[C/T]GTCAGGCTTCTCTTT | 137886 |
rs13278695 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441261 | ggcctgccaaagtgc[C/T]tgggttacaggcatg | 137886 |
rs13279410 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441369 | TATATATATATATAT[A/G]TATGTGTATATATAT | 137886 |
rs13279416 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441375 | tatatatatgtatgt[A/G]tatatatatgtatgt | 137886 |
rs13279425 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441385 | tatgtgtatatatat[A/G]tatgtatgtgtatat | 137886 |
rs13279635 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441395 | tatatgtatgtatgt[A/G]tatatatagtatgta | 137886 |
rs13281822 | snp | A/G | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420748 | GTTATATGACCCACT[A/G]AAACCAACTGTTCAA | 137886 |
rs16923442 | snp | A/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411844 | GTCACCTGAACAGTA[A/G]TGATACGTGATTTGT | 137886 |
rs16923447 | snp | A/G | 0.290706 | 0.248569 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417607 | TTCTTGTTGCCAGGA[A/G]TATTTTCATTAACAT | 137886 |
rs16923452 | snp | A/G | 0.448066 | 0.152544 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419034 | ATGCTGTCTGAAACA[A/G]TGCTGTGATTAATAG | 137886 |
rs16923455 | snp | C/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426615 | AAACTGCTGTCAGCT[C/G]CTCTTATCAACAGTG | 137886 |
rs16923457 | snp | A/T | 0.153997 | 0.230832 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429314 | GTCGTCGCTCCCTAA[A/T]ATAATCTGCTTCTAA | 137886 |
rs16923459 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429772 | TAAGTATTTTAACAA[C/G]TGAAGTTTGATTGTC | 137886 |
rs16923468 | snp | A/C | 0.0197882 | 0.097481 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430002 | TAACAAACGCAGGGG[A/C]TTTTAAGGGAGTAGG | 137886 |
rs16923469 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430135 | ACTAGGTCTCTACTG[A/C]GTGTGGCCTTCTTAG | 137886 |
rs16923472 | snp | C/G | 0.293482 | 0.24619 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433146 | AATTTTAACTCACTT[C/G]CTATGTATTTTAGTC | 137886 |
rs16923480 | snp | C/T | 0.281841 | 0.247964 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440610 | AAGTTACCCTCTACT[C/T]GTCCACATATTGTTG | 137886 |
rs17261333 | snp | A/G | 0.114036 | 0.209795 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426627 | GCTCCTCTTATCAAC[A/G]GTGGGTTTTCTGCCT | 137886 |
rs17261550 | snp | G/T | 0.272241 | 0.249009 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430226 | ATTAGTGAATGAGAT[G/T]TATGTGATAAGCAGT | 137886 |
rs17261584 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433042 | TGGTTCTTGAAGGCT[C/T]CCCAGTATGAGCCAC | 137886 |
rs28710905 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411864 | ACGTGATTTGTTCTT[C/T]TTTGTCTTGGATGCT | 137886 |
rs33952664 | in-del | -/AT | 0.49168 | 0.063958 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441349 | CTTGTTGTGATCAAC[-/AT]ATATATATATATATA | 137886 |
rs34005463 | in-del | -/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426203 | CCAGTGTTCTGAATC[-/T]TTTTTTTTTTTTTTT | 137886 |
rs34018318 | in-del | -/TT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432375 | ACCTTTCTAAATTTC[-/TT]TTTTTTTTTTTTTTT | 137886 |
rs34049384 | snp | A/G | 0.38286 | 0.211774 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413108 | GTACGATTAATGTTT[A/G]GAGATACTCTGGTAG | 137886 |
rs34052024 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440722 | CCCTTCCAAGCCCCC[-/T]TTCAGTTGCCTCGTG | 137886 |
rs34137759 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412924 | AGATGCTATAACTTT[-/C]CCCTGGCTAGTCAAT | 137886 |
rs34204639 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426202 | CCAGTGTTCTGAATC[-/T]TTTTTTTTTTTTTTT | 137886 |
rs34239812 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423014 | CCTTTTTTAAAATCT[-/G]GGTCTGGGCATGTGA | 137886 |
rs34354566 | in-del | -/TATT | 0.281577 | 0.247998 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446256 | AAATGAAATATGTGG[-/TATT]TAAACAGTCTCTATA | 137886 |
rs34406411 | snp | G/T | 0.382473 | 0.212016 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416054 | TTGTTTTTTGGGTTT[G/T]TTTTGAAAAAAACAA | 137886 |
rs34651909 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433735 | AGCCCAGGAGTTCGA[-/G]GACCACCCTGGGCAA | 137886 |
rs34689473 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424196 | TCCCCGACAATGAGG[-/A]AAAAAAAATTAAAAC | 137886 |
rs34805890 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438717 | GATGAGATTTTGGAC[-/T]TTTTGAGTTAATGCT | 137886 |
rs34813356 | in-del | -/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409959 | AGCAGATACCAACGG[-/T]AGTATTTCCCCTCAC | 137886 |
rs34836809 | in-del | -/A | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433611 | AGACCCTATCTCTTT[-/A]AAAAAAAAAAAAAAA | 137886 |
rs34843413 | in-del | -/TA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434358 | TTATGTATATGTGAA[-/TA]TATATATATATATAT | 137886 |
rs34989348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421298 | GTGGGAGAGATGACC[A/G]TAAGTTTCAGGAAGG | 137886 |
rs35031784 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414851 | TGTATGTTCCACATT[-/C]CCATGGGGCTAGTGG | 137886 |
rs35049059 | in-del | -/C | 0.45843 | 0.138046 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437329 | TTTCTTTTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 137886 |
rs35213875 | in-del | -/ATC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423080 | TTCTGGTGAGACGAA[-/ATC]ATCATCATCATCATC | 137886 |
rs35240470 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426254 | TCTGTCACCCAGGCT[-/G]GGAGTGCAGTGGCAT | 137886 |
rs35386041 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443135 | TTTCCTAAACCCCCT[-/A]CCTCGACCCCTGCCC | 137886 |
rs35435363 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422697 | TGGGGGTGCCCCAGT[-/G]GGGGTGGTGCTGCTT | 137886 |
rs35476562 | snp | A/G | 0.271972 | 0.249033 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417278 | AATATTTTTTGAGTC[A/G]TAGGACTCATTAAGG | 137886 |
rs35525023 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426867 | TGCAGCCGCCCCCTA[-/G]GCTGGCTTGCTCCTC | 137886 |
rs35545302 | snp | A/T | 0.00070775 | 0.0187982 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434372 | ATATATATATATATT[A/T]TTTTTTTTTCTATAC | 137886 |
rs35548366 | snp | A/G | 0.186737 | 0.241863 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443662 | AAAAAAAAAAAATTA[A/G]CCGCATGTGGTGACA | 137886 |
rs35601281 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58427463 | GCCATATGTTGTCTC[-/A]AAAAATATATAAATA | 137886 |
rs35647877 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437950 | AGACCTTTAAGGCAG[-/C]CCCCCCCCCCAACCC | 137886 |
rs35696176 | in-del | -/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409377 | ATCTAGGAAGATACT[-/G]GGTTAGTTTAACAAT | 137886 |
rs35749261 | in-del | -/T | 0.370974 | 0.218781 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423743 | TGGGTTTTTTTTTTT[-/T]AAGCCACTAAAGTTT | 137886 |
rs35752909 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425019 | CACGACTGGCCTTGC[A/G]TGCATGATGCGTTCC | 137886 |
rs35779085 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444052 | TGTGACATACACACA[-/T]TTTCTTACCTAGCTT | 137886 |
rs35885539 | in-del | -/C | 0.3333 | 0.235714 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437951 | AGACCTTTAAGGCAG[-/C]CCCCCCCCCAACCCC | 137886 |
rs35985125 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446831 | AGACAGAGTCTTACT[-/G]CTGTCTCCCAGGCTG | 137886 |
rs55658433 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436932 | CTTTATAGCAGTACA[A/C]ACAGACTAATACAGA | 137886 |
rs55704109 | snp | A/G | 0.49334 | 0.057322 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410688 | TATATATATATATAT[A/G]TGTATATATATGTAT | 137886 |
rs56072294 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447820 | GTTGTTACATGCTTA[A/G]TGTTAATGTAACAAC | 137886 |
rs56267708 | snp | C/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446727 | CATAGTTACCTTTTT[C/T]TGGGTCATATGCTGC | 137886 |
rs56316188 | snp | A/G | 0.370772 | 0.218893 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411252 | TGGGCCAGCACCGGA[A/G]GCGGGGGCGCGGGTT | 137886 |
rs56365831 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448757 | TCTGCTGAAGCCAGA[A/G]GCTTTTCCTTCTTCC | 137886 |
rs56390314 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447059 | CCACCTCTGCCTCCC[A/C]AAGTGCTGGAATTAC | 137886 |
rs56995270 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410752 | TGTGTATATATATAT[A/G]TGTGTGTATATATAT | 137886 |
rs57465869 | snp | A/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417764 | GTGTTTACTTCACCT[A/G]TATTCACCAAGTTGG | 137886 |
rs57482910 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410728 | TATATATATATGTGT[A/G]TGTATATATGTGTAT | 137886 |
rs57572802 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436387 | GACAGTATTATCCAC[C/G]TGACTCCCTGGAGGG | 137886 |
rs58529749 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410860 | CACCTCGTCCGCCTC[A/G]GCCTCCCAAAGTGCT | 137886 |
rs58772222 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435486 | GGGGTGGCAAATACA[A/G]GATATAATGGTTTAA | 137886 |
rs58957091 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450134 | TCATCACTTTCTCTA[C/G]AGTAAAGGCTGTCCT | 137886 |
rs59113842 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410788 | TATATATATATATAT[A/T]TATTTTTTTTTTTAG | 137886 |
rs59152897 | snp | C/T | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414404 | ATACTTTTAATATTT[C/T]GCTATATACTTTATT | 137886 |
rs59206925 | snp | C/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438345 | GTGCCACCTCCAGAC[C/G]CAGGAATGGTGGCGC | 137886 |
rs59493755 | snp | A/C | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448800 | CATCCTTAATTATTA[A/C]TTCTGGTTAGTTTTC | 137886 |
rs59858156 | snp | A/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414066 | TTCAGTATTGTTAGG[A/G]TTAGGATTGGATTTG | 137886 |
rs60146544 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410730 | TATATATATGTGTGT[A/G]TATATATGTGTATAT | 137886 |
rs60660641 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410716 | TATATATATGTGTAT[A/G]TATATATGTGTGTGT | 137886 |
rs61230751 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410754 | TGTATATATATATGT[A/G]TGTGTATATATATAT | 137886 |
rs61275761 | snp | C/T | 0.029116 | 0.117091 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425004 | AGCACTGCCGTGCAC[C/T]ACGACTGGCCTTGCA | 137886 |
rs61504051 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410714 | TGTATATATATGTGT[A/G]TATATATATGTGTGT | 137886 |
rs61634482 | in-del | -/TG | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410687 | ATATATATATATATA[-/TG]TGTATATATATGTAT | 137886 |
rs61732907 | snp | A/G | 0.00579705 | 0.053525 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411395 | CGGAAGATGGCGGAG[A/G]GCGGAGGCCCTGAGC | 137886 |
rs61732908 | snp | C/T | 0.0570934 | 0.159019 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411397 | GAAGATGGCGGAGGG[C/T]GGAGGCCCTGAGCCC | 137886 |
rs61732909 | snp | A/C | 0.0570934 | 0.159019 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411412 | CGGAGGCCCTGAGCC[A/C]GGCGAGCAGGAGAGG | 137886 |
rs61732916 | snp | C/G | 0.0387855 | 0.133748 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411437 | GAGAGGAGGTCTTCC[C/G]GGCCGCGGCCTCCGA | 137886 |
rs61733273 | snp | A/G | 1.66018e-05 | 0.00288108 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416905 | AATCTTCCAAGTCTA[A/G]TAGACCTAAAGCCAC | 137886 |
rs62512906 | snp | A/G | 0.287867 | 0.247116 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412173 | AGATTATTGATAAAA[A/G]TTTGACAAGTAAATA | 137886 |
rs62512907 | snp | A/G | 0.287606 | 0.247155 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414070 | GTATTGTTAGGGTTA[A/G]GATTGGATTTGTTAG | 137886 |
rs62512908 | snp | A/G | 0.287606 | 0.247155 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417734 | TCAAAAAGCAAGACT[A/G]GTAGAGTAAATACTG | 137886 |
rs62512909 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419562 | ATATCACAATCAGAA[C/T]TTGGATATGTCCTCC | 137886 |
rs62512910 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426851 | GGGATCCTGGAGACT[A/G]TGCAGCCGCCCCCTA | 137886 |
rs62512911 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435425 | CCTAAGAAGTATGCT[A/G]AAGGCATTGGGAAAG | 137886 |
rs62512912 | snp | C/G | 0.281577 | 0.247998 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436986 | ATTGCTCTAAAGATA[C/G]ATGAAGATGTGGAAG | 137886 |
rs67257878 | snp | G/T | 0.228842 | 0.249103 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448108 | AGAAACTACAGTTTT[G/T]CCTTGTATTTTACAG | 137886 |
rs67526441 | in-del | -/AATT | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439951 | TTATATCATAATATT[-/AATT]GTGATATTAATAATA | 137886 |
rs71248190 | in-del | -/TCA | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423120 | TCATCATCATCATCA[-/TCA]ATAGAGGGCAGTAGA | 137886 |
rs71248193 | in-del | -/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432596 | CCATGTTAGCCAGGG[-/G]TGGTCTCGATCTCCT | 137886 |
rs71248194 | in-del | -/ATATATATATATATATATATATATATATATATATATAT | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441368 | TATATATATATATAT[lengthTooLong]GTATGTGTATATATA | 137886 |
rs71248196 | in-del | -/T/TT | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448190 | TTTTTTTTTTTTTTT[-/T/TT]GATATGGAGTTTTGC | 137886 |
rs71521414 | snp | G/T | 0.375 | 0.216506 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423441 | TTTTTTTTTGTTGTT[G/T]TTTTTTTTTTTTGAC | 137886 |
rs71521415 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448323 | GGATTACAGGCATGC[A/G]CCACCATGCCTGGCT | 137886 |
rs71521416 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448807 | AATTATTACTTCTGG[G/T]TAGTTTTCCATTGCC | 137886 |
rs71557721 | in-del | -/TCTCTGTTGATGTCAG | 0.382473 | 0.212016 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424930 | CAGTCAACACCTTTC[-/TCTCTGTTGATGTCAG]TCAGAATATCAATCA | 137886 |
rs71557722 | in-del | -/C | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433743 | AGTTCGAGACCACCC[-/C]TGGGCAACATAGTAA | 137886 |
rs71557723 | in-del | -/ATTA | 0.387453 | 0.208822 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439948 | CCATTATATCATAAT[-/ATTA]ATTGTGATATTAATA | 137886 |
rs71557725 | in-del | -/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448173 | AAAGGTCAGCAATTC[-/T]TTTTTTTTTTTTTTT | 137886 |
rs72665340 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430916 | CAGGCATTTGCAAAA[A/G]GAATACAGGGAGGTT | 137886 |
rs73246940 | snp | G/T | 0.331874 | 0.236213 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423444 | TTTTTTGTTGTTGTT[G/T]TTTTTTTTTGACACG | 137886 |
rs73246945 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427080 | TAGGACTGGCAATAC[C/T]ATATAAAATTAATGA | 137886 |
rs73683573 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418401 | TTGAATTTCTGAATA[C/T]ACAGAACTCTTCCCA | 137886 |
rs74274677 | in-del | -/ACA | | | cds-indel, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448584 | TCATTTATTCATTCA[-/ACA]CATTTTTCTAGGAAA | 137886 |
rs74697834 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419834 | ATGGGGGTGCAGCCA[A/G]GAAGGCTTTCATAGG | 137886 |
rs74741912 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436385 | CAGACAGTATTATCC[A/G]CGTGACTCCCTGGAG | 137886 |
rs74789200 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443190 | TTCCAGCTTCATTGA[A/G]AAAATAGAACCTGAC | 137886 |
rs74799247 | snp | A/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443656 | AAAAAAAAAAAAAAA[A/T]AATTAGCCGCATGTG | 137886 |
rs74884939 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431505 | GCCAGCTTTTGACTA[C/T]TACAAATAAAGCTGC | 137886 |
rs74963323 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431081 | CACCCAACTGAAACT[A/C]TCCTTCATAGCCTAC | 137886 |
rs74987758 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417653 | AATACCATCCCTGGG[A/G]AAGAAACGTCAGTTT | 137886 |
rs75027308 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418498 | GTCTAGGCCAGATGT[C/G]TTATAAAATGTCTAA | 137886 |
rs75063235 | snp | G/T | 0.123452 | 0.215605 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431797 | TGGTTTTATTTTATT[G/T]GTCTAATAACTAATG | 137886 |
rs75091764 | snp | A/C | 0.000484572 | 0.015558 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446087 | AGCTTCTTTACCAAC[A/C]GTGTCCTGTTTGCTG | 137886 |
rs75174710 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442261 | TGATGATGTGAGCCT[A/G]TGTGTTCACAAACCC | 137886 |
rs75310791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434670 | TTTATAAAGGATATA[A/C]TGCTATCTGTATGTA | 137886 |
rs75647258 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444958 | GCCCAAATGCTCATA[A/G]AACTTTTATACTAGT | 137886 |
rs75746278 | snp | C/T | 0.00162347 | 0.0284447 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439619 | TGATAACTTTTTTCC[C/T]CCCTTTTTAAAAGAG | 137886 |
rs75963467 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429304 | TTCTGTGTTTGTCGT[C/T]GCTCCCTAAAATAAT | 137886 |
rs76001820 | snp | A/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443660 | AAAAAAAAAAAAAAT[A/T]AGCCGCATGTGGTGA | 137886 |
rs76047339 | snp | C/G | 0.0741063 | 0.177655 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451857 | TCTATTCAGTTATCT[C/G]TGCTCACTGAGATAA | 137886 |
rs76059945 | snp | C/T | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431926 | TTACTTTCCCATTCT[C/T]TAATTGGATTATTTT | 137886 |
rs76174685 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437240 | CAAAGGACTTGTCTG[C/T]GTTGTGTCCATACCC | 137886 |
rs76218226 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438161 | CTACTGTAAGCCTTG[A/G]TGGCTTTCGCATGGT | 137886 |
rs76359991 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417566 | CTTAAGAGATGAGAA[C/T]CAGGTGTCTTTTATT | 137886 |
rs76507813 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448873 | ACAAATTTATTATCT[G/T]CACAATTCTGTAGGT | 137886 |
rs76586491 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424244 | AGAAAAAAAAAAAAA[A/G]GCCTGTAACTAGAAT | 137886 |
rs76642901 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416498 | ATGGAAGAAGCTGAC[A/G]TTAGTGTGAACATCT | 137886 |
rs76734001 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437329 | ATTTCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 137886 |
rs76765601 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419249 | TCTAATGCTAAGTGT[A/G]TACTTCCTTTGATTT | 137886 |
rs76829590 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413071 | TGGCAAATTGTTTGC[A/C]GTCTTAATCCAGTGG | 137886 |
rs76910939 | in-del | -/AAA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424242 | AAAGAAAAAAAAAAA[-/AAA]GCCTGTAACTAGAAT | 137886 |
rs76980309 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437129 | ACCAAAGTATTGATA[A/G]AAATATGGACAGTGA | 137886 |
rs77038094 | snp | A/G | 0.0376037 | 0.131863 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410968 | TTCACTCTCAGTGCT[A/G]ATTCACGCTGTGGTG | 137886 |
rs77142954 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435569 | AACTAGGTGGGGGAA[A/G]TTTTGATTGGCTAAG | 137886 |
rs77202721 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440937 | TAATTTTAGGTCACA[A/G]GTTTACTTGGAAATT | 137886 |
rs77212900 | snp | C/T | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433500 | GAATTTGCAGCCAGG[C/T]GTGGTGACATGCATC | 137886 |
rs77249198 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426204 | CAGTGTTCTGAATCT[C/T]TTTTTTTTTTTTTTT | 137886 |
rs77327359 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412812 | CTGGTGGTGGTGTAA[A/G]GATTAAATAATGTTA | 137886 |
rs77390279 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445775 | TAGGATCCAAAATAA[A/C]TTTAATATAATGAAA | 137886 |
rs77391173 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414987 | ATTTAAAATACATCT[A/G]TCTATATCTATTTCT | 137886 |
rs77510231 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424243 | AAGAAAAAAAAAAAA[A/G]AGCCTGTAACTAGAA | 137886 |
rs77611703 | snp | C/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420406 | CAAAAAGGCAATTAA[C/G]TGAATCTCTTGAAAC | 137886 |
rs77764606 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418939 | TAATATTTGAGTTCT[G/T]ATCATAAGATTACTG | 137886 |
rs77913714 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440210 | TTATATGCCTCTTTC[A/T]GATTACCTGGTTTCA | 137886 |
rs77972490 | snp | A/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443659 | AAAAAAAAAAAAAAA[A/T]TAGCCGCATGTGGTG | 137886 |
rs78043930 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427899 | ATTTATGTAAGAGGA[A/G]GAGGAAGAAAACTCA | 137886 |
rs78259649 | snp | A/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446779 | AAAAGTACAACCTGC[A/T]TTTTTTTTTTTTTTT | 137886 |
rs78386822 | snp | C/T | 0.123798 | 0.215808 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451830 | CTTAGTGCAAACCTG[C/T]CTCCCATTCATTCTA | 137886 |
rs78479974 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442798 | GGCTTTTGAGCTGGC[A/G]TGTATAATGATAAAA | 137886 |
rs78611058 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417806 | ATTGAACTTGTGCAC[A/G]CATGTATTCTCTCTC | 137886 |
rs78719196 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438089 | GCATCTCCAGCCGCA[A/G]CTCAAAAAGCCCCAG | 137886 |
rs78742767 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431397 | TCAGAGTTATTGCTT[A/G]TATCACAACTTTGTT | 137886 |
rs78959420 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419747 | AGAGAGTCACATAAT[C/G]AAAATGACCAGAGGA | 137886 |
rs79015298 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418499 | TCTAGGCCAGATGTC[C/T]TATAAAATGTCTAAC | 137886 |
rs79167023 | snp | C/T | 0.00193329 | 0.0310308 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439803 | AGAAAAATACCTTTG[C/T]TGAACATGAATTTTT | 137886 |
rs79194026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422792 | CAAAAACAGGCTCAG[A/G]ATTGGCAAAAATCAT | 137886 |
rs79200908 | snp | A/C | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443638 | TCTCTACTAAAAATC[A/C]AAAAAAAAAAAAAAA | 137886 |
rs79334943 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441410 | GTATATATAGTATGT[A/G]TGTATGTTCTTAATT | 137886 |
rs79397365 | snp | A/C | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411831 | AGGGAAGTAGACAGT[A/C]ACCTGAACAGTAATG | 137886 |
rs79665026 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416503 | AGAAGCTGACGTTAG[C/T]GTGAACATCTTCAGG | 137886 |
rs79690901 | snp | A/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443657 | AAAAAAAAAAAAAAA[A/T]ATTAGCCGCATGTGG | 137886 |
rs79833433 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431734 | ACTTGGTATTGTCAC[A/T]ATTTTTAATTTTAGC | 137886 |
rs79843456 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446394 | TTAACATAGTAAAAC[C/T]TTTTGGGGACTTTAT | 137886 |
rs80109784 | snp | G/T | 0.0744748 | 0.178019 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410916 | CCGGCAGAGTTCTGC[G/T]TTTAGCAAATTATTC | 137886 |
rs80120308 | snp | A/T | 0.0741063 | 0.177655 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409327 | CCTAAGTGCTTATAT[A/T]CTAGGTTGAACAAAG | 137886 |
rs80220161 | snp | A/G/T | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420167 | AATTTTTTTGTTTTC[A/G/T]TATAAGAAAATGGTT | 137886 |
rs80308594 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413762 | CAAACTGCAGACTCG[A/G]AAATGTTTTTTTGCA | 137886 |
rs111373353 | snp | G/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424911 | TTTGAGAACGTCAAT[G/T]TTGCAGTCAACACCT | 137886 |
rs111448387 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449741 | TGCTGTTCTCTGGGC[C/T]TGTTGACTGTCTCAG | 137886 |
rs111496210 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425682 | TTGCTTAGTTCTCGA[A/G]TTCTGCTATTTCAGC | 137886 |
rs111613266 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427675 | GGAGGGCTTATGTGT[A/G]GAAATAGCTTCAGTT | 137886 |
rs111632899 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420971 | ACTTGATTCCCCCAA[A/C]AACATACAGAAAATA | 137886 |
rs111661561 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425376 | CATGTTTTGCAGGCA[A/G]CCTTGTGTGGCAATG | 137886 |
rs111694535 | snp | C/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426832 | AGACCCCCCTCCAGG[C/T]CTGGGGATCCTGGAG | 137886 |
rs111981301 | in-del | -/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421356 | GTTTTTTTTTTTTTT[-/T]AAAGCTATTAAGACT | 137886 |
rs111989848 | snp | G/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441441 | TTGTATCACTTCCCA[G/T]TTTTACTTAATATTT | 137886 |
rs112065079 | snp | A/T | 0.00129915 | 0.0254536 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439785 | GGTAAAAATCCTAAA[A/T]TGAGAAAAATACCTT | 137886 |
rs112251930 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430113 | AAATCTAAAGATCTC[A/G]TCACTAACTAGGTCT | 137886 |
rs112330317 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432885 | GATATGCCTAGAAAC[A/G]TGTCTTTTTAAAAAA | 137886 |
rs112555566 | snp | A/C | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448278 | TCCCAGGTTCAAAAG[A/C]TTCTCCTGCCTTAGC | 137886 |
rs112563596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430985 | CCCCCCAATGGTTAC[A/G]TTTCACATGATTGTA | 137886 |
rs112576564 | in-del | -/TGTG | 0.5 | 0 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410687 | ATATATATATATATA[-/TGTG]TATATATATGTATAT | 137886 |
rs112634164 | snp | C/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425708 | TCAGCAACATTTATA[C/T]GAGTCGTGTTAAGGG | 137886 |
rs112893775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425212 | GTGCTTTCTCTGATA[C/T]TCCTAACACGCATGA | 137886 |
rs112996215 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450847 | CACACTGGGAGTGCT[A/G]CCAGAACTACCACAG | 137886 |
rs113103762 | snp | A/G | 0.115088 | 0.210473 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409725 | CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTA | 137886 |
rs113336249 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431445 | TAGCATTTTATATAG[A/G]TATACCACAGTTTAA | 137886 |
rs113374514 | snp | A/G | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426085 | TTTAAGCTCAATAAC[A/G]TCTCCATTCTTCTCT | 137886 |
rs113449055 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426479 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAACC | 137886 |
rs113571668 | snp | G/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418235 | GATGGAGAAGGACTC[G/T]GTCTCCAAAAAAAAA | 137886 |
rs113734006 | snp | C/T | 0.265727 | 0.249505 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432468 | GCTGACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 137886 |
rs113765530 | snp | C/T | 0.5 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426927 | CTAATAAGGTTTTGC[C/T]AATTGGCAAGTTATT | 137886 |
rs114137316 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431249 | AGCACTTTGGGAGGC[C/G]GAAGCAGGCAGATCA | 137886 |
rs114200883 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412645 | TTTCCTATTATAAAC[C/T]CACATCACTAAGAGG | 137886 |
rs114463328 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442461 | TGAGCAGGAAATAAA[A/G]AGAAGCAAGTAAAAC | 137886 |
rs114602768 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422038 | CCAAAGTCAAGTCAA[A/G]ACAAAACCAAAGCAA | 137886 |
rs114706574 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437952 | GACCTTTAAGGCAGC[A/C]CCCCCCCCAACCCCC | 137886 |
rs114741977 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450914 | TCTCAGTGCCGTAAT[A/G]TAGAGGAATTCTCAA | 137886 |
rs114860212 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447694 | TTATTCTGTCTTCCA[A/G]TCTGAATATAGACAA | 137886 |
rs115121005 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425094 | GTCAATGGGCACTCC[A/G]TGGTCCGGCCAGGTC | 137886 |
rs115263671 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432986 | TTTCATTATTCGTCA[A/G]TGGTTTGAAATGATC | 137886 |
rs115266085 | snp | A/G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450408 | TCAGCTTAGCTTTTC[A/G/T]CCACTATGTAACAAG | 137886 |
rs115313265 | snp | C/T | 0.145305 | 0.227022 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451048 | GTCAAAATCATCTTC[C/T]GAAGAAAATGATTTC | 137886 |
rs115313905 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428822 | AAATACGAGAACTCA[A/G]GAATCATAGGCAACT | 137886 |
rs115375259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419501 | AGAAAGACCCTCAGG[A/G]TATAGTCTGATGCCT | 137886 |
rs115397004 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413976 | TATTTAGTTGTATAC[A/T]CTGTCCCAGTTTTCC | 137886 |
rs115546921 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445349 | TGCAAAGCAGTGCTT[A/G]AATCAGATGTGTTTA | 137886 |
rs115612494 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416049 | TTTGTTTGTTTTTTG[A/G]GTTTTTTTTGAAAAA | 137886 |
rs115726863 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416007 | GGAGCATTTTAATCT[A/G]TTTTGTTATGATTTT | 137886 |
rs116070177 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422234 | GCAATTCAAAGTTCA[A/G]TGAATATTGGGGGGC | 137886 |
rs116116136 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447305 | AAAGATTAAAATTTT[A/G]TGATTTTTATTATGA | 137886 |
rs116243269 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413264 | GATTTGGTGTATCAA[A/G]TACAGTATCTAAGTA | 137886 |
rs116310847 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448913 | AGGTTAAGAGTTTCG[C/T]GGTGCCAAGATCAAT | 137886 |
rs116413518 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442470 | AATAAAAAGAAGCAA[A/G]TAAAACAGAAATGAA | 137886 |
rs116580290 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413777 | GAAATGTTTTTTTGC[A/G]TATCAGAGTAGATTT | 137886 |
rs117150111 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435555 | GAAGAGCTGCGAGCA[A/G]CTAGGTGGGGGAAGT | 137886 |
rs117263755 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418104 | AAATTAGCTGGGCAT[G/T]GTGGCACGAGCCTAT | 137886 |
rs117296999 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438921 | GTTTTGGATCATGGA[A/G]GCAGATCCCTCATGA | 137886 |
rs117306192 | snp | A/G | 0.04875 | 0.148319 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449314 | TCCCACCCACCCCCC[A/G]CTCCACTCCTGTGTT | 137886 |
rs117574955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418199 | AGAGCCGAGATGGCG[C/T]GACTGCACTCCAGCC | 137886 |
rs117638264 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417584 | GGTGTCTTTTATTGC[C/T]GTGAGTTTTCTTGTT | 137886 |
rs117700179 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450502 | TGATTTAGATATTCT[A/G]TGGCAATCGAGGTAT | 137886 |
rs117723461 | snp | A/G | 0.00542542 | 0.0518003 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434532 | ATTTGTATTCTATTT[A/G]TTATGTAGAGTGGGA | 137886 |
rs117808026 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420008 | TATGTAGCCAGTTGC[A/G]GATACAGCCTTGAAG | 137886 |
rs117875276 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435614 | ACTGTAGAAATTGAT[A/G]CTAATTTCAAGATAG | 137886 |
rs117964966 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434590 | TTAGTGCACTACGGG[A/T]TTTCAAGAAGTAGTT | 137886 |
rs118060485 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439212 | TCGGATATTTCCTTA[C/T]AGCAATGCAAATGGA | 137886 |
rs118070618 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424558 | GTGAAGTCCACATCT[A/G]TTTTTGTGCTGAAGT | 137886 |
rs118104017 | snp | C/T | 0.0741063 | 0.177655 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449316 | CCACCCACCCCCCGC[C/T]CCACTCCTGTGTTAA | 137886 |
rs138120094 | snp | A/G | 0.00147694 | 0.0271347 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416909 | TTCCAAGTCTAATAG[A/G]CCTAAAGCCACAGTC | 137886 |
rs138203376 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449408 | TTATTACAGCATCAA[C/T]TCTAAATCCAAAATC | 137886 |
rs138326859 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429212 | AGGTGACTTCCATTC[C/T]TCGTTTCCAGGGCAC | 137886 |
rs138489340 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441196 | CACGTGTCTTACTAT[A/G]TTGCCCAGGCTGGTC | 137886 |
rs138604581 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410101 | CTATTTCTTTTTACC[A/T]TTGCATCCCTTGGGC | 137886 |
rs138745059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428938 | GTTCTTGTCCTCTAC[C/G]TTATACCACCTATAA | 137886 |
rs138772147 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422023 | TGAAAGACTTTACCC[C/T]CAAAGTCAAGTCAAA | 137886 |
rs138793334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442474 | AAAAGAAGCAAGTAA[A/G]ACAGAAATGAAAATA | 137886 |
rs138807574 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437901 | CTAGTGCTACTAATC[A/G]AGATGATGGGAAGAA | 137886 |
rs138947708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433049 | TGAAGGCTCCCCAGT[A/G]TGAGCCACTTTGGCT | 137886 |
rs139231981 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438766 | GGGGGACTATTGAGA[A/T]GGGATGATTGTATTT | 137886 |
rs139340822 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411811 | AGAAAGGTTACTGTG[C/G]CCGCAGGGAAGTAGA | 137886 |
rs139425363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439264 | AACACCCATATCAAT[C/T]TTCAGAACTTTCTCC | 137886 |
rs139443442 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449607 | AATAATAGTTACACA[C/T]GTTCCTGTTCAAAAA | 137886 |
rs139630842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430270 | GGGATCAGCAAGCAA[A/G]CCAGTTGCCGTGCTG | 137886 |
rs139662221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444891 | CTGTGTACTCTGAGA[G/T]AGAAGCTTTTTGAAT | 137886 |
rs139754955 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425690 | TTCTCGAATTCTGCT[A/G]TTTCAGCAACATTTA | 137886 |
rs139833462 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420229 | ACAAATACACTTTTA[C/T]TCTGATAATACAGCT | 137886 |
rs139865369 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411572 | CCTCGGCGGAGCCTT[G/T]CCCCGACCCCGTCTG | 137886 |
rs140014824 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438767 | GGGGACTATTGAGAA[C/G]GGATGATTGTATTTT | 137886 |
rs140047668 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422208 | CCTTTAGGCCACACC[C/T]GTGTTCTGAAGCAAT | 137886 |
rs140267467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414545 | ACATTTTCTTAATTA[C/T]GTTTTGAGATTTTTT | 137886 |
rs140279875 | in-del | -/TTCT | 0.00557542 | 0.0525036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440668 | AATGTTTCCAGTGTA[-/TTCT]TTGGTGCATCCTTTG | 137886 |
rs140606874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438623 | TACCCAATGCCTATA[A/C]CACCATTCTATCTTA | 137886 |
rs140707447 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440933 | TCTTTAATTTTAGGT[C/T]ACAGGTTTACTTGGA | 137886 |
rs140748211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436613 | GGGCCTGTGGGAGGT[A/G]TTTGGATCATGGGGT | 137886 |
rs140767526 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428132 | AGTATTCAGTAGCAA[A/C]CCTTGAGATTCAGTA | 137886 |
rs140799873 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440240 | AAAGGAGAGAATTGT[A/G]AAGGGTTGTCGATGA | 137886 |
rs141016193 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419347 | TGCTTATTTTCATGG[C/T]CCACCTCCTTGGGCG | 137886 |
rs141030370 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412851 | CTATGCAAAATTCCT[A/G]CATTATCCTGGCTCA | 137886 |
rs141099399 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421540 | AAATACCATGTATTT[G/T]TCATACCAACTTTCC | 137886 |
rs141163454 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417176 | AAGAAACTTACGGAA[A/T]AATTACCTTAAAATA | 137886 |
rs141165676 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441268 | CAAAGTGCCTGGGTT[A/G]CAGGCATGAGCCACT | 137886 |
rs141213580 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435696 | TAATTTATTGTTAAA[G/T]GAAAATAAACCACAA | 137886 |
rs141269370 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431673 | GTTGTGCCATTTTAT[A/G]TTCCCACATATATGA | 137886 |
rs141492506 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441988 | TGTTCCAGAGAAAAC[A/C]ACTATGTCCCCTAGT | 137886 |
rs141627214 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413279 | GTACAGTATCTAAGT[A/T]TTGATAATCTTTCCT | 137886 |
rs141672623 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411576 | GGCGGAGCCTTTCCC[C/T]GACCCCGTCTGGGGA | 137886 |
rs141688141 | snp | C/G | 0.0741063 | 0.177655 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409779 | TGGCCAGGCTGGTCT[C/G]AAACTCCTGACCTCA | 137886 |
rs141803286 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449422 | ACTCTAAATCCAAAA[C/T]CTTATCTGAGTCTCA | 137886 |
rs141817480 | in-del | -/TA | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432906 | TTTTAAAAAAGCCTC[-/TA]TGATAATTTTGACAT | 137886 |
rs141881781 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443639 | CTCTACTAAAAATCC[A/C]AAAAAAAAAAAAAAA | 137886 |
rs141917359 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433406 | CAGTCTCGATCTTTA[C/T]GTTTTGTATCACAAT | 137886 |
rs141924292 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418616 | TACATGACAACAGGA[A/G]TCATAATTTCAGGAT | 137886 |
rs141953500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432701 | ATAATTGTTACCAAC[C/T]GACACAATATTGATA | 137886 |
rs141981219 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429975 | AAAATTACTGTCTAA[A/T]TTATTTACTTTTAAC | 137886 |
rs142130822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444572 | TGGTTATCAGTGAGG[C/T]GGAGGTAAAGAGGAC | 137886 |
rs142205995 | in-del | -/A | 0.0333695 | 0.124785 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422256 | TTGGGGGGCAGGGAT[-/A]GGGGCTGATACACAT | 137886 |
rs142335123 | in-del | -/CATTC | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414848 | TTAATGTATGTTCCA[-/CATTC]CATGGGGCTAGTGGC | 137886 |
rs142349909 | in-del | -/TG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423440 | TTTTTTTTTTGTTGT[-/TG]TTTTTTTTTTTTGAC | 137886 |
rs142414560 | in-del | -/AT/TATATATATATATATATGTATGTG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441351 | GTTGTGATCAACATA[-/AT/TATATATATATATATATGTATGTG]TATATATATATATAT | 137886 |
rs142475145 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451339 | AGAGTCATTTTCATG[A/G]ATTATTTTTACTACT | 137886 |
rs142512563 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439357 | ATTTACATATAAATT[A/G]CTGTCTTAAAATTTA | 137886 |
rs142626793 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435324 | AGTGGAGGTTAAATT[C/T]GTCTTTTAGAAGACT | 137886 |
rs142751711 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425649 | GCCTTGTTTGACTTT[A/C]TTGTGGTCTCAGCTA | 137886 |
rs142777492 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437437 | GGTTCAAGCAATTCT[C/G]CTGCCTCAGCCTCCC | 137886 |
rs142817000 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442834 | GATTTGAAGCTGATG[G/T]TTCTGCAGAAGAACA | 137886 |
rs143162858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428955 | TATACCACCTATAAA[C/G]GTCAGTTCCATATGG | 137886 |
rs143228930 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424605 | ATCTGAAACTCTTCT[C/G]CTGTTGCATCAGGCC | 137886 |
rs143288804 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450196 | CATTTGAATAGGCCG[C/T]GAATTTCCCAAATCA | 137886 |
rs143348291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436485 | ATCTGACATCCCCTA[C/T]CTCGACACTGAATGA | 137886 |
rs143367412 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430295 | GTGCTGGAGGCTGAA[C/G]TTGCCCTTAGAATCA | 137886 |
rs143381624 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426500 | GGTGTGAACCACCGT[A/G]ACCGGCCCAGTGTTC | 137886 |
rs143443010 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427578 | ATGTAATGACATGGG[A/T]TATAGGGAGTAAGCC | 137886 |
rs143584397 | snp | C/T | 0.371582 | 0.218444 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410685 | ATATATATATATATA[C/T]ATGTGTATATATATG | 137886 |
rs143726635 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413383 | TAAAGTATGTATCAA[A/G]AGTTTAAAAGAATTA | 137886 |
rs143909430 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444153 | AGATTACAAAAATAA[C/T]AGGGAGGCAACTTGG | 137886 |
rs144079191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438487 | GCCCTGTATATGGGA[C/T]GTGGCATCAAGGATT | 137886 |
rs144190585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435435 | ATGCTGAAGGCATTG[G/T]GAAAGGTGGGAAGCT | 137886 |
rs144200214 | in-del | -/CAA | 0.274393 | 0.248807 | cds-indel, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448582 | ATTCATTTATTCATT[-/CAA]ACACATTTTTCTAGG | 137886 |
rs144225472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429602 | GAGAGCTGGTCTGTT[C/G]TTTCCTCTATCTTAC | 137886 |
rs144390512 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450471 | TCCTCATTTTTTACC[A/G]ACAGTCTATTCATGA | 137886 |
rs144435226 | in-del | -/C | 0.125874 | 0.217008 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436127 | TGCAGTCTAGCACTT[-/C]CTATGTAAATGTGAC | 137886 |
rs144482262 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418050 | GTTCAAGACCAGCCT[A/G]GCCAACATGGCAAAA | 137886 |
rs144538671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434843 | CTAAGCCACTGTCCT[C/G]CTTACTGTTGACAGG | 137886 |
rs144554150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438679 | TACAGGATTATAGGT[A/G]GAAAGAAGATGGCTT | 137886 |
rs144593059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417661 | CCCTGGGGAAGAAAC[A/G]TCAGTTTTCCCATTA | 137886 |
rs144607725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412980 | TGTGTAACTTAATGT[C/T]CTTTCCCTAATTTAA | 137886 |
rs144851216 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421970 | CAGAGATGTTAATAC[A/C/T]GGAGATATATTTGTA | 137886 |
rs144951026 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419362 | TCCACCTCCTTGGGC[A/G]GTATTTGAAATCAAA | 137886 |
rs144958693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436386 | AGACAGTATTATCCA[C/T]GTGACTCCCTGGAGG | 137886 |
rs145095253 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436072 | AATGCCCTGGTATGA[C/T]CACACAGCACACCTA | 137886 |
rs145104346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431118 | CACTCACACCCACCC[C/T]GTCTCTCATGCCATC | 137886 |
rs145145494 | in-del | -/ATAT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441349 | CTTGTTGTGATCAAC[-/ATAT]ATATATATATATATA | 137886 |
rs145222173 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420494 | TGACATCCTAAAACA[C/T]ATTCCCTTTAAAAGA | 137886 |
rs145382553 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412584 | CATAGTTGGTTCAGT[A/G]GTAGTAAACAGTATC | 137886 |
rs145626258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436921 | CTCAAGTATTCCTTT[A/G]TAGCAGTACAAACAG | 137886 |
rs145723266 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447737 | AATAGACCTTGAGAT[A/G]AGTATGTTTGAGTTT | 137886 |
rs145769698 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431478 | ATTCATTTATTGAGG[A/G]ATATTTTAGTTGCCA | 137886 |
rs145833181 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428431 | ATGACATAATTGCAT[A/G]CAAAGAAAACTGTAA | 137886 |
rs146197428 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449879 | GTGCTTCTGCTGCTA[C/T]AACGTTGTCAAGAAA | 137886 |
rs146315366 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433947 | TTATTTTAGACATTG[A/G]TAGTTTCTTGGAAGG | 137886 |
rs146367858 | snp | C/T | 0.0741063 | 0.177655 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409748 | TATTTTTAGTAGAGA[C/T]AGGATTTCACCACGT | 137886 |
rs146494444 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421360 | TTTTTTTTTTTTAAA[G/T]CTATTAAGACTGTGA | 137886 |
rs146620297 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450541 | ATGCTCCTTTCTTCA[A/G]GGCCGCCCTAGCATT | 137886 |
rs146623941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445557 | TGATTGATGTACTTA[C/G]TCAACTTTACACAGT | 137886 |
rs146699565 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444878 | TTTTATCACTTTACT[A/G]TGTACTCTGAGAGAG | 137886 |
rs146821159 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426019 | TTCTTTCCCAGAGAG[G/T]TGTCCCTGAAACCAC | 137886 |
rs146856947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440688 | TGGTGCATCCTTTGC[A/T]TCTCTTCATGTGATT | 137886 |
rs146995083 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448438 | CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 137886 |
rs147055282 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448234 | GCTGGAGTGCAATGG[C/T]ATAATTTCTGCTCAC | 137886 |
rs147090272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429076 | TAAAAACCGTTAACC[A/G]TAAAGGAGATAGGAA | 137886 |
rs147309421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418670 | ATTTGGTTAAGGTGC[C/T]GACCACCACAGCACT | 137886 |
rs147419036 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443007 | TCAACAGCTGTGAGC[C/T]GACTGAAGCCTGACT | 137886 |
rs147435677 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439198 | TAAATTACCCAGCCT[C/T]GGATATTTCCTTATA | 137886 |
rs147452386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419823 | AGGTTGGATAGATGG[A/G]GGTGCAGCCAGGAAG | 137886 |
rs147528862 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424746 | ATACTTAATATTTGT[A/G]TATTCATGACCTTTC | 137886 |
rs147779266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435480 | TATATGGGGGTGGCA[A/G]ATACAGGATATAATG | 137886 |
rs147786923 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431510 | CTTTTGACTATTACA[A/G]ATAAAGCTGCTGTGA | 137886 |
rs147889154 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413075 | AAATTGTTTGCAGTC[G/T]TAATCCAGTGGATCA | 137886 |
rs147892344 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409771 | CACCACGTTGGCCAG[A/G]CTGGTCTGAAACTCC | 137886 |
rs148009005 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418323 | GTCACATATCTCTTA[C/T]AGCTTTTTCTTTGGA | 137886 |
rs148322409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441569 | GAATTAATGTTGGAC[C/T]GCACATCCTTGTTAG | 137886 |
rs148374867 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436532 | TCACACCATGATGTT[C/T]AGATGGTTTAGATGT | 137886 |
rs148445732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435243 | ACAGGGTTATACTCC[A/G]TAAAGGAATAGAAGG | 137886 |
rs148567945 | in-del | -/G | 0.0603597 | 0.1629 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443510 | GAATTAACATAACTT[-/G]GCATGGGCACAGTGG | 137886 |
rs148580965 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409325 | GGCCTAAGTGCTTAT[A/G]TACTAGGTTGAACAA | 137886 |
rs148586344 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425297 | ATCCTCTCTCCACTT[C/G]TTTCGTTGTCATGAC | 137886 |
rs148632868 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444266 | GTTGTTAGGATAATT[A/G]TAATGCTAATAGCCA | 137886 |
rs148933248 | snp | G/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448213 | AGTTTTGCTCTTGTT[G/T]CCCAGGCTGGAGTGC | 137886 |
rs148956547 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413939 | GTGTCCCTCAGCCCG[-/T]CCACACACATGTTCA | 137886 |
rs149176151 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420523 | GATTTATCAATAAAA[C/T]ATTAAATATCTTTTA | 137886 |
rs149249863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417901 | CAGCATGAGTCTCCC[A/G]AGAAGAAGCACACAC | 137886 |
rs149250312 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449739 | ACTGCTGTTCTCTGG[A/G]CTTGTTGACTGTCTC | 137886 |
rs149319166 | snp | C/T | 0.187369 | 0.242028 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410683 | GTATATATATATATA[C/T]ATATGTGTATATATA | 137886 |
rs149495694 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423474 | GGAGTCTTGCACTGT[C/T]GCCCAGGCTGGAGTG | 137886 |
rs149499456 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438085 | TGCTGCATCTCCAGC[C/T]GCAGCTCAAAAAGCC | 137886 |
rs149543550 | in-del | -/TG | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433300 | TCTAGTTACTAAAAC[-/TG]TTGGTTTTAAAATTA | 137886 |
rs149807720 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425876 | TGGGCCACTTTAGAC[A/T]TGCCGTTATTGTTCT | 137886 |
rs149824684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440304 | AGCATGCATGTCTGC[C/T]ATCAGTAATGACCAA | 137886 |
rs149876587 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443422 | TGTAAAAGTTTTACT[A/G]TGGCTTGATCAATTG | 137886 |
rs149965663 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431105 | AGCCTACCATTTGCA[C/T]TCACACCCACCCCGT | 137886 |
rs149988906 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420479 | TTCACATCAAAATGA[C/T]GACATCCTAAAACAT | 137886 |
rs150041772 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412100 | AGCGCACCAAATCCC[A/G]TTTTATCAGATACTA | 137886 |
rs150139529 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410047 | TACCCGTTTACATGT[C/T]TCTTTTCCCTACTAG | 137886 |
rs150263868 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432726 | TTGATATACTAAAGA[C/T]GAACAGTTACGTGTC | 137886 |
rs150300103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422343 | TCAGAAAGGAACTAC[C/T]ACCAGGGCTGGATCT | 137886 |
rs150312869 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432375 | TACCTTTCTAAATTT[-/C]TTTTTTTTTTTTTTT | 137886 |
rs150505940 | snp | C/T | 0.0298908 | 0.118541 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449518 | GTGATTTCTGGGACA[C/T]AATTCCAACTGTGCA | 137886 |
rs150558477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442057 | AGAACATTCCATCAT[C/T]GAAGAAATAAATGCC | 137886 |
rs150627622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425680 | ATTTGCTTAGTTCTC[A/G]AATTCTGCTATTTCA | 137886 |
rs150632998 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437534 | TTCACCATCTTGGCC[A/C]GGCTGATCTTGAACC | 137886 |
rs150873826 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411701 | CCTTCCACCCCACGT[A/G]TGATGTAAAAATAGC | 137886 |
rs150997706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435397 | CAGGATACCAAACAA[A/C]GGCAACAAATGCCCT | 137886 |
rs151066704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413491 | TTTTCTTAAGAGTTA[C/T]GCAGTTCGTGCAGCT | 137886 |
rs151207547 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430334 | AAACTCAGTGAGAAA[C/G]TATATGATTTCCTAT | 137886 |
rs151332103 | snp | A/C | 0.00438332 | 0.0466095 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451602 | TAATTTCCCTTGGCG[A/C]ACCTTTGTCAGGGAC | 137886 |
rs180869040 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420619 | ATCCTTTTCCCATTA[A/G]CTTTTATTAATAAAA | 137886 |
rs180884337 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432720 | ACAATATTGATATAC[G/T]AAAGACGAACAGTTA | 137886 |
rs180893818 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451167 | TTGAAATTTTCTTGT[C/T]TTTATCAGTTGAGTG | 137886 |
rs180904774 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427081 | AGGACTGGCAATACT[A/T]TATAAAATTAATGAG | 137886 |
rs180942165 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411048 | GACTAGATGGAGAGG[C/T]TGCAATTTTTCATCA | 137886 |
rs180977886 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443495 | TGACAGCTAAATATT[A/G]GAATTAACATAACTT | 137886 |
rs181109841 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416183 | CAGAAAAAATTCTAT[A/G]CAATACTGAAATATT | 137886 |
rs181199074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438737 | GAGTTAATGCTGGAA[C/T]GAGTTAAAACTTTGG | 137886 |
rs181202149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447141 | TAGTACACTTACTTT[A/G]TTCATAACTTACCTG | 137886 |
rs181206654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429890 | AGGTTATTAATCTTA[C/T]GTAAAGGTAATTTTT | 137886 |
rs181221297 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424909 | GTTTTGAGAACGTCA[A/G]TGTTGCAGTCAACAC | 137886 |
rs181422276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443323 | CTGAGGGAATTACAA[C/T]CTACATCCTTTCCTG | 137886 |
rs181435544 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410408 | ACAGAGCGAGGCTCC[A/G]TCTCAAAAACAAAAA | 137886 |
rs181593690 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426857 | CTGGAGACTGTGCAG[C/T]CGCCCCCTAGGCTGG | 137886 |
rs181632807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424735 | TCCGCTAGAGAATAC[A/T]TAATATTTGTATATT | 137886 |
rs181648115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438537 | TAATGTCTGCCCTGC[C/T]GGGTTTCAGACTTCT | 137886 |
rs181749669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429585 | TTCCTTTACTGCAAA[A/G]TGAGAGCTGGTCTGT | 137886 |
rs181836374 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426657 | TCCACCCCAGTGATA[C/T]TTGGGTGAAACCATC | 137886 |
rs181840825 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410044 | TCTTACCCGTTTACA[C/T]GTCTCTTTTCCCTAC | 137886 |
rs181841070 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442773 | GACTAGCGAGTAGGC[A/C]TTCTTGGTAGGCTTT | 137886 |
rs181934118 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415006 | ATATCTATTTCTGAT[G/T]CATTTTCTATTATGT | 137886 |
rs182021837 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451694 | TACCCAAATAAAAAG[A/G]TTCAGGTGCTTCTTT | 137886 |
rs182022676 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416718 | TCAGAAAGGAATCAT[C/G]TGAAGCAGCAGCTTT | 137886 |
rs182035559 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447901 | GGTAAAATTTGCACT[A/G]AAGTTTCTTGATGCA | 137886 |
rs182035809 | snp | A/C | 0.00106315 | 0.0230314 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430656 | CAAGAGCTTCAGGTG[A/C]TGATAAATCTAAGGT | 137886 |
rs182107656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418200 | GAGCCGAGATGGCGC[A/G]ACTGCACTCCAGCCT | 137886 |
rs182120533 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431860 | TGAACATCGTTTCAT[A/G]TGCTTCCTTGCCATT | 137886 |
rs182129966 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449816 | GAGTATCAACTTATC[A/C]GTTTGTTCTTCTTTT | 137886 |
rs182301686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432985 | ATTTCATTATTCGTC[A/C]ATGGTTTGAAATGAT | 137886 |
rs182322972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436864 | TACAGCCTGCAGAAC[C/T]ATGAGCCAAAATAAA | 137886 |
rs182349555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422833 | TCTTGAAGACCCTCT[C/G]TTTATTTCTCAGTCT | 137886 |
rs182362333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435227 | AACCAGAGTTATATA[C/T]ACAGGGTTATACTCC | 137886 |
rs182366673 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440019 | TGTGGCCCTCTAAGC[C/T]GTATACATGTGTTAT | 137886 |
rs182570518 | snp | A/C/G | 0.00914312 | 0.0669923 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424688 | GTTGGAGTACAAGGC[A/C/G]GGGGGGGGGGCTCTG | 137886 |
rs182614219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425222 | TGATATTCCTAACAC[A/G]CATGATGCCATATTC | 137886 |
rs182624302 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417804 | ACATTGAACTTGTGC[A/T]CGCATGTATTCTCTC | 137886 |
rs182643783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431304 | ATGGTGAAACTACAG[A/T]GTTATACAAATGGAG | 137886 |
rs182843089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422344 | CAGAAAGGAACTACT[A/G]CCAGGGCTGGATCTA | 137886 |
rs182860926 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434057 | TGAAGGAAGTGGGAA[C/T]CATGGAGTACAGCTC | 137886 |
rs182950805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444592 | GTAAAGAGGACCTTT[G/T]CATTCAGTGTCTCAT | 137886 |
rs182952470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425578 | CTTTTACCCTCTTTT[C/T]GGCCGTAGAGAAGTA | 137886 |
rs182958891 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409359 | GAGGCAATCGTGGAA[A/G]AGTATCTAGGAAGAT | 137886 |
rs182961007 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440586 | TAGAAATTTAAAATA[C/T]GTTGGTAAAAGTTAC | 137886 |
rs183178629 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411664 | ACAAGTGCCCAAGCC[A/T]CCAGCGCTGGTGCTT | 137886 |
rs183184047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443893 | AGCTTGTCCAGCTAT[C/T]TGTCTGTGTGGTTCT | 137886 |
rs183188794 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427335 | AAGCGTGGTGGTGCA[C/T]GCCTGTAGTCCCAAC | 137886 |
rs183234001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412767 | GTCTGATCCTGTGTC[C/T]TCATTTGTAAACTGA | 137886 |
rs183255464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444267 | TTGTTAGGATAATTA[C/T]AATGCTAATAGCCAA | 137886 |
rs183484762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427536 | GTGAAATTAATGCAG[C/G]ATATTTTAAAGGTGT | 137886 |
rs183499833 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431092 | AACTCTCCTTCATAG[C/T]CTACCATTTGCACTC | 137886 |
rs183623562 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409867 | GCCCAGCCTCAAATG[C/T]CTTTATACATCAAAA | 137886 |
rs183727018 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417367 | TTCGTTTTTAAGGAT[A/T]TGTGTGTTTCTTGAA | 137886 |
rs183756736 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448012 | TTGATTTTGAAATTG[C/T]TTGATCATACAATAA | 137886 |
rs183820214 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423514 | GGTCTCAGCTCACTG[A/C]AAGCTCCGCCTCCTG | 137886 |
rs183882286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413803 | GATTTTCATAGCTCC[C/T]TTCATCCCCCTCAAA | 137886 |
rs183976036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420096 | ATAAAAATTTAGTGA[C/G]AAAACTATAATACAA | 137886 |
rs183981493 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450317 | TACCTTCCACAGCTT[A/G]CTTGGAAATATCCTC | 137886 |
rs183982657 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432618 | CGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 137886 |
rs184010682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435542 | GCAGAATCACTGGGA[A/G]GAGCTGCGAGCAACT | 137886 |
rs184166420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442257 | AGCATGATGATGTGA[A/G]CCTATGTGTTCACAA | 137886 |
rs184192833 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423889 | CAAACGTTTTCCCAC[C/T]ACAACCTTCTCAGTC | 137886 |
rs184210331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435868 | AGTGGTTCTCAGCTA[C/T]GTAAGACCCATTGTC | 137886 |
rs184284334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426394 | TTGTATTTTTTAGTA[A/G]AGACGGGGTTTCACC | 137886 |
rs184440538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427920 | AGAAAACTCAGTAAA[A/G]TAGAGAAGGAGATGT | 137886 |
rs184465142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436433 | TGGAACCCAAGATGA[A/G]TCTTTATCACGTAAG | 137886 |
rs184602657 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424393 | ATGAGTAATTGGGAA[A/G]CAGGTATTGTTGAGT | 137886 |
rs184649918 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410230 | CCATCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 137886 |
rs184656960 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442904 | GTGCTTGCCACTCTC[A/T]CTTACCTGAGATTTG | 137886 |
rs184663806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426701 | GTTCCTCCCACATTC[C/T]GGCTCCGTGACAGAC | 137886 |
rs184718149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425816 | GAATCATACCGTTCT[C/T]CTCCACCAACATCGT | 137886 |
rs184843273 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409663 | TTCCCGGGTTCAAGC[A/G]ATTCACCTGTCTCAG | 137886 |
rs184882199 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414546 | CATTTTCTTAATTAC[A/G]TTTTGAGATTTTTTT | 137886 |
rs184897574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444794 | TTTATGTATCCTCAA[A/G]TCAGTTCTAAAATTA | 137886 |
rs184898625 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428779 | GCAATGGTTAAGAGA[A/G]TAAGAACTGACAGTA | 137886 |
rs184946360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432776 | ACATTCTTACAAGTA[A/G]CATTTCTCAACCTGG | 137886 |
rs184960943 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427218 | TCACGCCTGTCATCT[G/T]AGCACTTTGGGAGGC | 137886 |
rs184964994 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411136 | CTGCCCTCTAGGGCG[C/G]CCTACAGTGCCTTTA | 137886 |
rs184966694 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451171 | AATTTTCTTGTTTTT[A/T]TCAGTTGAGTGCCTA | 137886 |
rs185012969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415906 | TATATTTTAAAAGTT[A/G]ACTAATAGAATTTTC | 137886 |
rs185045718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445708 | CAGTTAAATGAGGAA[A/C]GGATGCAAAGTTAGG | 137886 |
rs185133778 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429609 | GGTCTGTTCTTTCCT[C/T]TATCTTACTCAGTTT | 137886 |
rs185197531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430146 | ACTGAGTGTGGCCTT[A/C]TTAGGGAGAAGGGAC | 137886 |
rs185201534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416344 | AATTTATGGTCTTGT[G/T]TGTTCAGAAACTCAT | 137886 |
rs185210159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447228 | TACATTTTAACTGAA[A/G]CCTAAGATAAATCCT | 137886 |
rs185272950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432317 | CCAGTTGCTCCAGCA[G/T]CACTTCTTGAAAGGC | 137886 |
rs185395136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419727 | AGGGACAAAATTCCA[A/G]GAACAGAGAGTCACA | 137886 |
rs185410145 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450218 | CCCAAATCATCAAGT[C/T]CTGGTTTCTTTATAT | 137886 |
rs185693839 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437799 | TATGTAGTAGAGAAG[A/G]AGAAAGTGTTTTCAG | 137886 |
rs185719621 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422363 | GGGCTGGATCTAGGC[C/G]TTCCTTTCAGGAGCC | 137886 |
rs185739348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434635 | AATAAATGGTTGCTG[A/G]GGGTGTAGGTATTCT | 137886 |
rs185805694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420639 | TATTAATAAAAGAAT[C/T]ACAATTAGGTCACAA | 137886 |
rs185853756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443505 | ATATTAGAATTAACA[C/T]AACTTGCATGGGCAC | 137886 |
rs185959883 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424821 | AGTATAATGCTGGAC[C/T]GCCATATAGATAAAT | 137886 |
rs185973759 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438628 | AATGCCTATACCACC[A/G]TTCTATCTTAGAAGT | 137886 |
rs186106795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438897 | TTACTGAGGTGGGGC[C/T]GGTGGGAGGTTTTGG | 137886 |
rs186246316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424957 | TCAGTCAGAATATCA[A/G]TCACAACGTATGTCC | 137886 |
rs186279841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430974 | CCCCAATGGTTCCCC[C/T]CAATGGTTACGTTTC | 137886 |
rs186287260 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447955 | AATCTTTTGATCAAA[G/T]AAGTTGAAAATTTGT | 137886 |
rs186358785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426946 | TGGCAAGTTATTTAA[A/C]CTCCTTCAGTCTTAG | 137886 |
rs186542193 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410508 | ATCTGCTTTTTTTCT[A/T]TTTTGAGACGGATCC | 137886 |
rs186573789 | snp | A/C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443331 | ATTACAACCTACATC[A/C/G]TTTCCTGCCATTTGC | 137886 |
rs186645526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417390 | TTCTTGAAGCCACTC[C/T]ATGGAGCCTCTGCAG | 137886 |
rs186656161 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448127 | TGTATTTTACAGAAT[C/T]ATGACTGTTGTGAAC | 137886 |
rs186707563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428099 | GTTTGGCAATGAGAA[G/T]ATAACTCAGAACCTT | 137886 |
rs186721342 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413938 | TGGTGTCCCTCAGCC[C/T]GCCACACACATGTTC | 137886 |
rs186723856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444654 | TTGTGTAAGGAACGC[A/T]GGACTCTTGGCACAG | 137886 |
rs186860656 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431111 | CCATTTGCACTCACA[A/C]CCACCCCGTCTCTCA | 137886 |
rs186920088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433092 | TCTAGTTTTAAAATA[C/G]ATATCACATAATAAC | 137886 |
rs186955762 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418132 | TATAATTCCAGCTAC[A/T]TGGGAGGCTGAGGCA | 137886 |
rs186962522 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448883 | TATCTTCACAATTCT[A/G]TAGGTTAGGAGTCCA | 137886 |
rs186966028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431426 | TTCCTTTTTAATTCC[C/T]GAGTAGCATTTTATA | 137886 |
rs187123829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421881 | ATCTAAATGAAATCA[A/G]TATAACAAACAAAGC | 137886 |
rs187125968 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451836 | GCAAACCTGCCTCCC[A/G]TTCATTCTATTCAGT | 137886 |
rs187179075 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424695 | TACAAGGCGGGGGGG[G/T]GGGCTCTGATCTCCA | 137886 |
rs187288275 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425582 | TACCCTCTTTTCGGC[C/T]GTAGAGAAGTATGCA | 137886 |
rs187291285 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409587 | TGTTTTTAAGACGGA[G/T]TCTCTCTGTGACACC | 137886 |
rs187295792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440659 | CACATTGGCAATGTT[G/T]CCAGTGTATTCTTTG | 137886 |
rs187389794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417084 | TATTATTCCAAGATC[A/G]AGGCAGATTTGGATA | 137886 |
rs187508752 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411836 | AGTAGACAGTCACCT[C/G]AACAGTAATGATACG | 137886 |
rs187514659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443926 | GCATGTCTTTTAGTC[C/T]CTCTGTGACTCGGTT | 137886 |
rs187518210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427338 | CGTGGTGGTGCACGC[C/T]TGTAGTCCCAACTGC | 137886 |
rs187527792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423026 | ATCTGGTCTGGGCAT[A/G]TGACTTGTTTAGTAA | 137886 |
rs187765849 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409668 | GGGTTCAAGCAATTC[A/T]CCTGTCTCAGCCTCC | 137886 |
rs187770677 | snp | A/C | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435236 | TATATATACAGGGTT[A/C]TACTCCATAAAGGAA | 137886 |
rs187781652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425355 | CATCCGCCAAAAGTC[A/G]TTCACCATGTTTTGC | 137886 |
rs187792722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441412 | ATATATAGTATGTAT[A/G]TATGTTCTTAATTTT | 137886 |
rs187964215 | snp | C/G/T | 0.00279258 | 0.0372817 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449864 | CTGTTAAAAATGGTG[C/G/T]TGCTTCTGCTGCTAT | 137886 |
rs188021552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427596 | TAGGGAGTAAGCCAG[C/T]GGGAAAGAGGGAAGA | 137886 |
rs188062192 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425864 | CAAATCATAACATGG[A/G]CCACTTTAGACTTGC | 137886 |
rs188122027 | snp | A/G | 0.00110442 | 0.0234732 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447598 | AATAGATGATGTGCC[A/G]TATTAATAAGGACAA | 137886 |
rs188124502 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430177 | TATCTTTTGACTGTT[A/G]ACACTGCTTTTCCTT | 137886 |
rs188288306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413004 | AATTTAAATCCATTT[C/G]TTCTTTTTATGTGAA | 137886 |
rs188323574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444310 | CCAACTATATAAAAG[C/T]ACCATTTGAAGTGCT | 137886 |
rs188354153 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420263 | CAACTAGCAAAGCAG[C/T]TGCGCTAACACCCAT | 137886 |
rs188368866 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450774 | TAGATTTGGAATTCA[C/T]CTTTCTCCAGGGTCA | 137886 |
rs188373281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432711 | CCAACTGACACAATA[C/T]TGATATACTAAAGAC | 137886 |
rs188572046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435587 | TTGATTGGCTAAGCG[A/G]AAACCAACATAACTG | 137886 |
rs188595365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424017 | CCAATGCAAAGGTAG[A/G]CCAGTCAGCTTCTGA | 137886 |
rs188617795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436145 | ATGTAAATGTGACAG[G/T]TATAAAAACAGAAAA | 137886 |
rs188827893 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431903 | CTTTTCAAGGAAATA[G/T]CTCTTCATTACTTTC | 137886 |
rs188839823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423682 | CCTCATGATCCGCCA[G/T]CCTCGGCCTCCCAAA | 137886 |
rs189026554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443223 | GAATTCACATTCTTA[C/T]TATGTTTCCCTCCAG | 137886 |
rs189030690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426740 | TGCTCAGGCTCCACT[A/G]GGCTCGGTCACGTTG | 137886 |
rs189094110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418425 | CTTCCCACCTTTTTA[C/T]TGTTGTTTTTAGCTC | 137886 |
rs189104194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440400 | TTTTTTCAAGTCATG[A/G]AAGTGCAATATGTAA | 137886 |
rs189121441 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424467 | AAAGGTAGTCAACCA[C/G]AATGCAAGCCTTCCA | 137886 |
rs189280674 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428787 | TAAGAGAGTAAGAAC[G/T]GACAGTAGACCATGG | 137886 |
rs189286652 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424706 | GGGGGGGGCTCTGAT[A/C]TCCACTCGTCTGGTC | 137886 |
rs189288965 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444962 | AAATGCTCATAGAAC[G/T]TTTATACTAGTAATA | 137886 |
rs189397558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436810 | ATTGTAAGTTCCCTG[C/T]GGCTTCACCAGAAGG | 137886 |
rs189532311 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426587 | AGGGTTACTTTTACT[A/G]GGCCTTGCCAAAAAA | 137886 |
rs189538011 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409938 | CAGCACCTAGCATGG[G/T]GCACACAGCAGATAC | 137886 |
rs189550030 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442609 | CTGTAAAAATGTTAC[A/T]TAGTACCCTCACATA | 137886 |
rs189658639 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429749 | TTTGGAATTGGATTG[G/T]AGAGTTATAAGTATT | 137886 |
rs189674873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416577 | AAATGGTTTGTTACC[C/T]AAAACAGATTTTGAC | 137886 |
rs189925634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419771 | CAGAGGAACCAGAAA[A/G]AGAACCAGCAGAACT | 137886 |
rs189925810 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450270 | TACCTCTTTCCACAT[G/T]TTACTATAATCAGCA | 137886 |
rs189930564 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415957 | ATGCCCTGTTCTTCT[C/T]GGAGGTAGTTTTCAT | 137886 |
rs189945374 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446424 | TTCATTTAAAAATTT[A/G]TGATAATTTTGATTG | 137886 |
rs190083161 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422398 | TCAGAAGAATCCGAG[A/G]AAACAATAACTTCAC | 137886 |
rs190107752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434791 | AACATCTTAATGTGA[C/T]AATCAGTGAATTAAT | 137886 |
rs190170454 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432334 | ACTTCTTGAAAGGCA[C/T]TCCTTTCTCCATTGA | 137886 |
rs190180929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414698 | AATGAACTCATGCCA[C/T]ATGATGCCATATGGC | 137886 |
rs190187558 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410232 | ATCCTGGCCAACATG[G/T]TGAAACCCCGTCTTT | 137886 |
rs190223815 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438416 | TCCAACCCATGAGAG[A/C]AGCCACAGGGCCAGA | 137886 |
rs190334400 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424822 | GTATAATGCTGGACC[A/G]CCATATAGATAAATC | 137886 |
rs190344561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438698 | AGAAGATGGCTTGAA[G/T]CTCAGATGAGATTTT | 137886 |
rs190473357 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432956 | GCTGTAATGAAACTT[A/T]AATTTTGGTTTTCAT | 137886 |
rs190508109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443937 | AGTCTCTCTGTGACT[C/T]GGTTTCTTTTAGATA | 137886 |
rs190606755 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422305 | AGCCAAACTAACTCA[C/G]GGTCTTAAGAGACTG | 137886 |
rs190745423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425477 | CATCTGAAACAGGCT[C/T]GTTGGGATCACCATC | 137886 |
rs190747264 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451208 | CACATACAAAAACAA[C/T]TGCCATTTTTGTATA | 137886 |
rs190752951 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447996 | TACTGAAACGTGTCT[G/T]TTGATTTTGAAATTG | 137886 |
rs190764262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425023 | ACTGGCCTTGCATGC[A/G]TGATGCGTTCCTGCT | 137886 |
rs190767268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440517 | TAAAAACCAACGCAC[A/G]TGGCAGAATGTATGA | 137886 |
rs190992219 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410902 | CGTGAGCCACAGGCC[C/T]GGCAGAGTTCTGCTT | 137886 |
rs190992913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427281 | TCAAGACCAGCCTGG[C/T]TAACAGGGCTTAAAC | 137886 |
rs190997696 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411483 | AGGTGAGGCGAGGAG[A/C]CGGGGGAGGGAGCGC | 137886 |
rs190999610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443797 | TGGGCAACAGAGCAA[C/T]ACTGCATCCCAGAAA | 137886 |
rs191024732 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439279 | TTTCAGAACTTTCTC[C/T]GAGGAGTTTATTAAT | 137886 |
rs191025827 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443394 | TTTCTTTCTTAAAAA[A/T]TTTTCTTTTTAATGT | 137886 |
rs191253221 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427048 | AAATGTTAGCTATTA[A/C]TATTCATTTAGGAAA | 137886 |
rs191301008 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431250 | GCACTTTGGGAGGCC[A/G]AAGCAGGCAGATCAC | 137886 |
rs191420130 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418189 | GAAGTTGCAGAGAGC[C/T]GAGATGGCGCGACTG | 137886 |
rs191433498 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449673 | ATCAATTTACAAAAC[C/T]AGCGAGGCACCCTTC | 137886 |
rs191439327 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431676 | GTGCCATTTTATATT[A/C]CCACATATATGAGAG | 137886 |
rs191546352 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417621 | AATATTTTCATTAAC[A/G]TCTTTTTAGTACTGT | 137886 |
rs191548287 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448764 | AAGCCAGAAGCTTTT[A/C]CTTCTTCCTAGACAC | 137886 |
rs191556008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424032 | ACCAGTCAGCTTCTG[A/G]CAGTCTCAGGCCCTA | 137886 |
rs191557795 | snp | A/G | 0 | 0 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451988 | ACTTCGAGTTGTCCT[A/G]CCTTTCCATATTGAT | 137886 |
rs191567365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436284 | CGTAAAGTGGACTTT[A/G]CTTCCTGGAGATTTC | 137886 |
rs191578255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427504 | TGAGGTAGTGTCAAT[A/G]GAACGGAGAGAAAAG | 137886 |
rs191810873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417170 | AGCCAAAAGAAACTT[A/T]CGGAAAAATTACCTT | 137886 |
rs191817394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412485 | GGGTGCCAAAATAAG[C/G]AGTGCATAAAGCGAA | 137886 |
rs191824265 | snp | A/G | 0.00271671 | 0.0367556 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433128 | GCTGAATAATCCTTT[A/G]TGAATTTTAACTCAC | 137886 |
rs191831981 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441183 | GGTTTTGTAGAGACA[A/C/T]GTGTCTTACTATGTT | 137886 |
rs191833624 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425723 | CGAGTCGTGTTAAGG[A/G]GCTACGTGAGTTGTA | 137886 |
rs191845387 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58420001 | CACAAATTATGTAGC[C/T]AGTTGCGGATACAGC | 137886 |
rs192098727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423715 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 137886 |
rs192116017 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435598 | AGCGAAAACCAACAT[A/G]ACTGTAGAAATTGAT | 137886 |
rs192133550 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431070 | ACATGTGTAATCACC[C/G]AACTGAAACTCTCCT | 137886 |
rs192343484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426144 | GCCGGACCAACTCAG[A/C]CAAAGTGGAAAATTT | 137886 |
rs192572322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413511 | TTCGTGCAGCTTTCA[G/T]TAGATATTTCTTACT | 137886 |
rs192611674 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58444573 | GGTTATCAGTGAGGC[A/G]GAGGTAAAGAGGACC | 137886 |
rs192630352 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414199 | GTCATTATTCTGTAT[A/C/T]GTTGATTCTCTAGTA | 137886 |
rs192641720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444722 | TTCCAAATTAAAAAG[A/C]AATTCCTTAATATCT | 137886 |
rs192652268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428707 | TTGCCCCAAACATTC[A/G]TGAAGAATTAAAGTT | 137886 |
rs192714907 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409673 | CAAGCAATTCACCTG[C/T]CTCAGCCTCCCAAGT | 137886 |
rs192725111 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441570 | AATTAATGTTGGACC[A/G]CACATCCTTGTTAGT | 137886 |
rs192771146 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409653 | CAACCTCTGCTTCCC[G/T]GGTTCAAGCAATTCA | 137886 |
rs192789390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432550 | ACCACACCCAGCTAA[C/T]TTTTTGTATTTTTAG | 137886 |
rs192845384 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427657 | AAAGTGTGATTGTTA[A/G]TGGGAGGGCTTATGT | 137886 |
rs192993924 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450306 | ACAGCAGGCTGTACC[G/T]TCCACAGCTTGCTTG | 137886 |
rs193034633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419000 | ATCATTAAGATATTT[C/T]AGTGAAGGGTTTTCT | 137886 |
rs193051283 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449883 | TTCTGCTGCTATAAC[A/G]TTGTCAAGAAACTTG | 137886 |
rs193133399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435336 | ATTCGTCTTTTAGAA[A/G]ACTAATTAGCATGAA | 137886 |
rs193166253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445658 | CTCGTATTTCTAAAT[A/G]AAACTGGTTTGCTAA | 137886 |
rs193222767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431979 | TCTTTGTATATTTTA[A/G]TAGGTATGGGTCCTT | 137886 |
rs193287110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423496 | GCTGGAGTGTAGTGG[C/T]GAGGTCTCAGCTCAC | 137886 |
rs199571735 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441365 | TATATATATATATAT[A/G]TATGTATGTGTATAT | 137886 |
rs199734588 | in-del | -/ATCATC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423080 | TTCTGGTGAGACGAA[-/ATCATC]ATCATCATCATCATC | 137886 |
rs199883632 | snp | A/G | 9.94398e-05 | 0.00705053 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439656 | CCCTGGAGCTTCAGC[A/G]CCTTGTTCATGGTGG | 137886 |
rs199894539 | snp | A/G | 9.95966e-05 | 0.00705609 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416898 | AAGTGCAAATCTTCC[A/G]AGTCTAATAGACCTA | 137886 |
rs199917675 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446812 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCT | 137886 |
rs200008585 | snp | C/T | 0.000238513 | 0.0109179 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416952 | CGGACACCACCTCAA[C/T]GGTAAGTTTTATTTT | 137886 |
rs200027201 | snp | A/G/T | 1.65974e-05 | 0.0028807 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416886 | GAAGATGAAGTGAAG[A/G/T]GCAAATCTTCCAAGT | 137886 |
rs200127386 | in-del | -/ATAT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58434349 | CTTATGTATATGTGA[-/ATAT]ATATATATATATATA | 137886 |
rs200167918 | snp | C/G/T | 0.000448833 | 0.014974 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447534 | CTTAACACTGTGTTA[C/G/T]TCCAGCAACTAAAAT | 137886 |
rs200218974 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423443 | TTTTTTGTTGTTGTT[-/G]TTTTTTTTTTGACAC | 137886 |
rs200263793 | snp | C/G/T | 3.43349e-05 | 0.00414325 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446076 | ACACACAGGTAAGCT[C/G/T]CTTTACCAACAGTGT | 137886 |
rs200274268 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432628 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 137886 |
rs200283440 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423438 | GTTTTTTTTTTGTTG[-/T]TTGTTTTTTTTTTTT | 137886 |
rs200302061 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417580 | ACCAGGTGTCTTTTA[C/T]TGCTGTGAGTTTTCT | 137886 |
rs200302230 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441367 | TATATATATATATAT[A/G]TGTATGTGTATATAT | 137886 |
rs200336686 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448173 | TAAAGGTCAGCAATT[C/T]TTTTTTTTTTTTTTT | 137886 |
rs200378832 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424230 | TTAAGGTTATAAAAA[A/G]AAAAAAAAAAAAAAG | 137886 |
rs200394112 | in-del | -/TAT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441356 | TGATCAACATATATA[-/TAT]ATATATATATGTATG | 137886 |
rs200414947 | snp | G/T | 0.078151 | 0.181571 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423447 | TTTGTTGTTGTTTTT[G/T]TTTTTTGACACGGAG | 137886 |
rs200530804 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426893 | TCCTCCTCCCTGTAA[-/T]TTTTTTTTTCTCTGT | 137886 |
rs200765240 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447079 | GCTGGAATTACAGGC[A/G]TAAGCCACCGTGCCC | 137886 |
rs200837298 | in-del | -/CAC | 0.00874735 | 0.0655527 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426405 | GTAGAGACGGGGTTT[-/CAC]CACCATGTTAGCCAG | 137886 |
rs200866000 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415095 | GAGAAACTTAAAATC[C/T]AGTTGGGGAAATAAA | 137886 |
rs200891049 | snp | C/T | 1.66779e-05 | 0.00288768 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439626 | TTTTTTCCCCCCTTT[C/T]TAAAAGAGAGATTCC | 137886 |
rs200962765 | in-del | -/A/C | 0.342693 | 0.240852 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437951 | GACCTTTAAGGCAGC[-/A/C]CCCCCCCCCAACCCC | 137886 |
rs201070829 | in-del | -/A/TT | 0.0206163 | 0.0994139 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434370 | TATATATATATATAT[-/A/TT]TTTTTTTTTTTCTAT | 137886 |
rs201076095 | in-del | -/ATATA | 0.00409595 | 0.0450688 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434365 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTCTA | 137886 |
rs201097674 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441010 | TCTTTTTTTTTTTTT[-/T]GAGATGGGGTCTTGC | 137886 |
rs201181124 | snp | C/T | 0.00199794 | 0.0315433 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434402 | CCCAAAAGGTTCAGA[C/T]TTTGCTTAAACTGTG | 137886 |
rs201223319 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450179 | GTTTTAGTGGCTTTT[G/T]CCATTTGAATAGGCC | 137886 |
rs201308171 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410690 | TATATATATATATGT[A/G]TATATATATGTATAT | 137886 |
rs201309347 | snp | A/T | 0.277067 | 0.24853 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434369 | TATATATATATATAT[A/T]TTTTTTTTTTTTCTA | 137886 |
rs201331612 | snp | A/G | 0.000172144 | 0.00927589 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434422 | CTTAAACTGTGGAGC[A/G]ATGGTTTCAGTTTAG | 137886 |
rs201413839 | in-del | -/AAAAAAAAAAAA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418242 | AAGGACTCTGTCTCC[-/AAAAAAAAAAAA]AAAAAAAAAAAAATT | 137886 |
rs201450792 | snp | A/T | 0.0144233 | 0.0836876 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434371 | TATATATATATATAT[A/T]TTTTTTTTTTCTATA | 137886 |
rs201577324 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419212 | AGATTGTTCGCAATC[-/T]TTTTTTCTACGTATG | 137886 |
rs201581024 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438139 | TCGCTCTGAAGGGCA[A/C]AAGCCACTACTGTAA | 137886 |
rs201615961 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418269 | AAAAAAAAAAAAATT[A/G]ATAGTAATTCTGTGA | 137886 |
rs201680284 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423808 | TTGACAACCAAAAAC[A/G]CTGGTCATTCATAGA | 137886 |
rs201811200 | snp | A/T | 0.0207795 | 0.0997895 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434367 | TATATATATATATAT[A/T]TATTTTTTTTTTTTC | 137886 |
rs201868942 | in-del | -/TG | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410750 | ATGTGTATATATATA[-/TG]TGTGTGTGTATATAT | 137886 |
rs201903141 | in-del | -/ATCATCATC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423080 | TTCTGGTGAGACGAA[-/ATCATCATC]ATCATCATCATCATC | 137886 |
rs201936054 | snp | A/G | 1.71855e-05 | 0.00293129 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434423 | TTAAACTGTGGAGCA[A/G]TGGTTTCAGTTTAGA | 137886 |
rs202246575 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446816 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTACT | 137886 |
rs367640817 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441143 | ATAGGCACTGCCGAG[C/T]GCAGCTCATTTTTTT | 137886 |
rs367644152 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421045 | CCTTATGGATACTAA[A/G]CTAAAATAAAACACT | 137886 |
rs367840934 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432737 | AAGACGAACAGTTAC[A/G]TGTCTTTTGTGGTAT | 137886 |
rs367845302 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414330 | AAGTTCCCAGGTGTC[C/T]GTATAATAATCATTT | 137886 |
rs367868061 | snp | C/T | 9.02063e-05 | 0.00671528 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430666 | AGGTGATGATAAATC[C/T]AAGGTCAGTGCTCAA | 137886 |
rs367871454 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429250 | AGGGGAGGAGTGTTA[C/T]GGCAGCAGACAGCTG | 137886 |
rs367929276 | snp | A/G | 1.70455e-05 | 0.00291933 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434459 | GAGAATTGAGACCTT[A/G]CAATGAACCAACAAA | 137886 |
rs368119759 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414915 | AAATTGTTATTTGAT[C/T]GGAAGCATTTATTCA | 137886 |
rs368134031 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413498 | AAGAGTTACGCAGTT[C/T]GTGCAGCTTTCAGTA | 137886 |
rs368161833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430439 | ATAAAATACTTTTAT[G/T]TTCATAAGACTATGT | 137886 |
rs368294893 | snp | A/C | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410462 | GTCTAAATCAATTTC[A/C]GTTGAATGACGAGGG | 137886 |
rs368304235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426553 | CTCCATTTCTTCTAA[C/T]AAAAAGTGTGAAGTC | 137886 |
rs368325148 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449325 | CCCCGCTCCACTCCT[G/T]TGTTAAAGATTCAGA | 137886 |
rs368377509 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441589 | ATCCTTGTTAGTAGA[C/T]CTACAGTAAATCTAG | 137886 |
rs368403550 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58430017 | CTTTTAAGGGAGTAG[A/G]TCTCTTAAATCCAAA | 137886 |
rs368404827 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438831 | AGTGGTGGAATGATA[C/T]GGTTTGGATGTTTTG | 137886 |
rs368470827 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419977 | CGATTTTCACTTTGC[A/G]CTGGGTCTCACAAAT | 137886 |
rs368471768 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422265 | AGGGATAGGGGCTGA[A/T]ACACATTTTGTTAGT | 137886 |
rs368481198 | snp | A/G | 3.77743e-05 | 0.00434577 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447356 | AAAATATGATTTTTT[A/G]TATTACAAATTATTT | 137886 |
rs368482105 | snp | A/G | 1.66405e-05 | 0.00288443 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447542 | TGTGTTACTCCAGCA[A/G]CTAAAATAATATTGT | 137886 |
rs368491287 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424690 | TGGAGTACAAGGCGG[C/G]GGGGGGGGCTCTGAT | 137886 |
rs368623522 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435492 | GCAAATACAGGATAT[A/G]ATGGTTTAAGTCAAT | 137886 |
rs368649441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436726 | TTAAAAGAGCCTGGA[A/G]CCTCCCCTTCTCTCT | 137886 |
rs368710843 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409811 | GTGATCCGTCTGCCT[C/T]GGCCTCCCAAAGAGT | 137886 |
rs368824049 | snp | C/T | 0.000169986 | 0.00921759 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434536 | GTATTCTATTTGTTA[C/T]GTAGAGTGGGACTTA | 137886 |
rs369269876 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409512 | TTTCAGGAAGAAAAG[A/G]TCAGAGTGCTCTTCT | 137886 |
rs369362541 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422783 | TGCTGGTTCCAAAAA[C/G]AGGCTCAGGATTGGC | 137886 |
rs369365721 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433010 | AATGATCTTTTAGTC[A/C]AGTCTTATGGTAATT | 137886 |
rs369537469 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414908 | CCAAAGAAAATTGTT[A/G]TTTGATTGGAAGCAT | 137886 |
rs369702144 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421869 | TTGTGGAGGGAAATC[C/T]AAATGAAATCAATAT | 137886 |
rs369809976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423726 | AGGCGTGAGCCACCG[C/T]GCCCAGCCGGGGATG | 137886 |
rs370052274 | in-del | -/TT | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450718 | GTACCTAGAAAACTC[-/TT]TTATGCCTGCTTCTC | 137886 |
rs370067175 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426486 | GTGCTGGGATTACAG[A/G]TGTGAACCACCGTGA | 137886 |
rs370120245 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425662 | TTATTGTGGTCTCAG[C/T]TAATTTGCTTAGTTC | 137886 |
rs370132086 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449073 | TTCATCTCTATGACC[C/T]TTCTGTTACCACATC | 137886 |
rs370208032 | snp | A/C/G | 8.45221e-05 | 0.00650037 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446056 | TGATACAAAGATTCA[A/C/G]TAGTACACACAGGTA | 137886 |
rs370312261 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433362 | CTTTTTAAAACATGG[A/G]TTAAAAGGACCAATG | 137886 |
rs370533900 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419773 | GAGGAACCAGAAAAA[C/G]AACCAGCAGAACTTT | 137886 |
rs370588052 | snp | A/G | 5.03791e-05 | 0.00501867 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430618 | GGCAAGGGAACATGG[A/G]GCTGTCCCTCTGAAT | 137886 |
rs370605877 | snp | A/G | 0.000169986 | 0.00921758 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430528 | TTAAAGGTTTTACTC[A/G]AGTGAACATGAATAC | 137886 |
rs370668280 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444689 | CCAGATTGGCAGTGC[A/C/G]ATTACTTAGGCCCTC | 137886 |
rs370686138 | in-del | -/GG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424697 | CAAGGCGGGGGGGGG[-/GG]CTCTGATCTCCACTC | 137886 |
rs370700374 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58431650 | CAGCCAAACTATTTT[A/C]CAGAGTGGTTGTGCC | 137886 |
rs370716179 | snp | A/G | 1.66178e-05 | 0.00288247 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445964 | GGAGGATAAATCAAT[A/G]CTTAATGCAGTTGTT | 137886 |
rs370737616 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423414 | CAAATTGAAGAACAG[C/T]TGGGGGTGGGTTTTT | 137886 |
rs370758707 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447078 | TGCTGGAATTACAGG[C/T]GTAAGCCACCGTGCC | 137886 |
rs370884848 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417398 | GCCACTCCATGGAGC[C/T]TCTGCAGGTCTTTTG | 137886 |
rs370999975 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58433811 | AAGAAAAATGAACAA[A/G]TATATAGTTATTATT | 137886 |
rs371020425 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413939 | GGTGTCCCTCAGCCC[A/G]CCACACACATGTTCA | 137886 |
rs371040398 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451601 | TTAATTTCCCTTGGC[A/G]CACCTTTGTCAGGGA | 137886 |
rs371230643 | in-del | -/TCTGTTGATGTCAGTC | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424932 | GTCAACACCTTTCTC[-/TCTGTTGATGTCAGTC]AGAATATCAATCACA | 137886 |
rs371346170 | snp | A/G/T | 0.000232086 | 0.0107699 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447414 | GTCCGGAACTTTATT[A/G/T]TACAGTCTCGTCCTG | 137886 |
rs371374579 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436524 | CTCACAGATCACACC[A/G]TGATGTTTAGATGGT | 137886 |
rs371676747 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436480 | AGTGCATCTGACATC[C/T]CCTACCTCGACACTG | 137886 |
rs371678833 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449399 | CACAATCCATTATTA[C/T]AGCATCAACTCTAAA | 137886 |
rs371679201 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426568 | CAAAAAGTGTGAAGT[C/T]TCCAGGGTTACTTTT | 137886 |
rs371701339 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413545 | CTAACAGCTTGCTCT[A/G]AGAGTCTTTCAGAGT | 137886 |
rs371835210 | snp | A/G | 7.91969e-05 | 0.00629223 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434521 | TAAGATGTATTATTT[A/G]TATTCTATTTGTTAT | 137886 |
rs371859258 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434877 | ACTCTCATTGCATGT[A/G]TGCCTGAAATTCAGC | 137886 |
rs371869770 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422556 | TGGAACATTAGCAAA[A/T]CTTACCATTTGGCTA | 137886 |
rs372053615 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425842 | ATCGTATTTCAGTTC[C/G]TGACAGCAAATCATA | 137886 |
rs372241488 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426162 | AAGTGGAAAATTTCT[C/T]CCCTCCACACAGATC | 137886 |
rs372265443 | snp | A/G/T | 0.00177751 | 0.0297674 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434384 | ATTTTTTTTTTTTCT[A/G/T]TACCCAAAAGGTTCA | 137886 |
rs372315404 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441797 | ACAGAGATCAGTGGT[A/G]ATAATGCCATGTTAA | 137886 |
rs372390761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413117 | ATGTTTGGAGATACT[C/G]TGGTAGATGTTGCTA | 137886 |
rs372417333 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425438 | TGGTTTCAAATTTGG[G/T]CATGATGATATTTGC | 137886 |
rs372489627 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430120 | AAGATCTCGTCACTA[A/T]CTAGGTCTCTACTGA | 137886 |
rs372531623 | snp | C/G | 1.69657e-05 | 0.00291248 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439590 | CAGTGTAGTTTAATT[C/G]TTGGAAAACTTAATG | 137886 |
rs372658487 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417784 | CACCAAGTTGGTACA[A/G]TGTTACATTGAACTT | 137886 |
rs372747414 | in-del | -/TGTTTTT | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409572 | TTGTTTTTTGTTTTT[-/TGTTTTT]AAGACGGAGTCTCTC | 137886 |
rs372755332 | snp | A/G | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58445995 | CTTATTGATGATTCA[A/G]TGCCAACAACAAAAA | 137886 |
rs372798546 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58421191 | GTTTCCCCGAAGCAA[A/C]TGGGCTCTTTAAAGA | 137886 |
rs373012405 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411257 | CAGCACCGGAAGCGG[A/G]GGCGCGGGTTCGGGT | 137886 |
rs373020917 | snp | C/T | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416866 | TGGCCTTGGCAGAAT[C/T]GTATGAAGATGAAGT | 137886 |
rs373138314 | in-del | -/TA | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410759 | ATATATATGTGTGTG[-/TA]TATATATATATATAT | 137886 |
rs373192241 | snp | C/T | 1.66687e-05 | 0.00288688 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430566 | TAAATATAGTTCGAC[C/T]TTCAACTGGGAAAAT | 137886 |
rs373443139 | snp | A/G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443938 | GTCTCTCTGTGACTC[A/G/T]GTTTCTTTTAGATAA | 137886 |
rs373559127 | snp | C/T | 0.000317034 | 0.0125864 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416937 | GTCTTCAAGAGCCCA[C/T]GGACACCACCTCAAC | 137886 |
rs373562376 | in-del | -/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437318 | TGGTGGAAGAAATTT[-/C]TTTTTTTTTTTTTTT | 137886 |
rs373741046 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426380 | CCGGCTAATTTTTTT[-/T]GTATTTTTTAGTAGA | 137886 |
rs374034389 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413386 | AGTATGTATCAAAAG[C/T]TTAAAAGAATTAAAT | 137886 |
rs374083112 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423628 | TTTTAGTAGAGATGG[A/G]GTTTCACCGTGTTAA | 137886 |
rs374294909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424287 | AATCTGCAAAATATA[A/G]CACACAATTTAACTG | 137886 |
rs374319875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425654 | GTTTGACTTTATTGT[C/G]GTCTCAGCTAATTTG | 137886 |
rs374359866 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410342 | TGCTTGAACCCGGGA[A/G]GTGGAGGCTGCAGTG | 137886 |
rs374412669 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423441 | TTTTTTTTTGTTGTT[-/G]TTTTTTTTTTTTGAC | 137886 |
rs374428688 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417107 | TTTGGATAAAAAATA[A/G]AAATGATTAATATCA | 137886 |
rs374616602 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435814 | TATGATCAATAAGAG[A/T]TTTAGAAAAGACTCT | 137886 |
rs374631357 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449303 | CCTACTACAGTTCCC[A/T]CCCACCCCCCGCTCC | 137886 |
rs374690089 | in-del | -/T | 0.00262568 | 0.0361379 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439611 | AAACTTAATGATAAC[-/T]TTTTTCCCCCCTTTT | 137886 |
rs374693736 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58436205 | ACTACAAGTAGCATT[A/G]CATTCAAGGACTTGG | 137886 |
rs374722088 | in-del | -/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58424688 | GTTGGAGTACAAGGC[-/G]GGGGGGGGGGCTCTG | 137886 |
rs374809539 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410792 | TATATATATATATAT[A/T]TTTTTTTTTAGTAGA | 137886 |
rs374811967 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443837 | ATAAAATAAATTAAT[C/T]AACATAACTTTTTAG | 137886 |
rs374813018 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422873 | TCTCAGCTACTGTAA[C/G]CAGTTTTGGCTTCCC | 137886 |
rs374897585 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443355 | CATTTGCCTACAAAC[C/G]TTGTTGTACCAATTA | 137886 |
rs374920300 | snp | A/T | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446058 | ATACAAAGATTCAAT[A/T]GTACACACAGGTAAG | 137886 |
rs375104842 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425136 | TTGCCAGACCATTCT[C/G]TCCATATTCCCTTGC | 137886 |
rs375107034 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443253 | GCCTTCAAGCTGGTC[A/G]TTTCCATCCTCCTCT | 137886 |
rs375216372 | snp | C/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409706 | CTGGGACTACAGGCA[C/T]GCGCCACCACGCCCA | 137886 |
rs375304126 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437318 | TGGTGGAAGAAATTT[C/T]TTTTTTTTTTTTTTT | 137886 |
rs375334381 | snp | C/T | 0.000169986 | 0.00921759 | missense, intron-variant, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58439664 | CTTCAGCGCCTTGTT[C/T]ATGGTGGCCAAGTGA | 137886 |
rs375370415 | in-del | -/TAT | 0.472709 | 0.11358 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434368 | ATATATATATATATA[-/TAT]TTTTTTTTTTTCTAT | 137886 |
rs375542370 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412285 | CAAACCACCATCCAT[C/T]GTAACATACTGCTGA | 137886 |
rs375545929 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425880 | CCACTTTAGACTTGC[A/C]GTTATTGTTCTCCCC | 137886 |
rs375555510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415980 | GTTTTCATATCATTT[A/G]TGTGTCTAAAAGGAG | 137886 |
rs375629292 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411685 | GCTGGTGCTTTGTCT[C/G]CCTTCCACCCCACGT | 137886 |
rs375644865 | snp | A/G | | | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451650 | TAGCATATTATCTGA[A/G]TATCCTGTTACTGTT | 137886 |
rs375686813 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438375 | CCACCAGCAACCTGA[A/G]CCTGGAAAAGCCACA | 137886 |
rs375795339 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426558 | TTTCTTCTAACAAAA[A/G]GTGTGAAGTCTCCAG | 137886 |
rs375829447 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426751 | CACTGGGCTCGGTCA[C/T]GTTGGGCTGGCCCGA | 137886 |
rs375884067 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58440843 | CTGTATTCTCTTCTC[C/T]TGATAGAGACTGGCA | 137886 |
rs376012974 | in-del | -/AT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432907 | TTTAAAAAAGCCTCT[-/AT]GATAATTTTGACATC | 137886 |
rs376094334 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58412307 | TACTGCTGAGCTTTG[A/C]GAATGTGGAAATAAG | 137886 |
rs376229785 | snp | A/G | 0.000132532 | 0.0081393 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58433206 | GTTCTTTTTGTAAGC[A/G]GTCTGAATATATCTA | 137886 |
rs376690916 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446858 | GCTGGAGTGCAGTGG[C/T]GGAATCTCAGCCCAC | 137886 |
rs376786040 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58438835 | GTGGAATGATATGGT[G/T]TGGATGTTTTGTCCC | 137886 |
rs376847366 | snp | C/G | 2.17924e-05 | 0.00330087 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445878 | TATATTTTACACATT[C/G]AGATTTGTGTTTAAT | 137886 |
rs376858382 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423695 | CAGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 137886 |
rs377018516 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58415511 | GACCATAAGGAGATA[C/T]AACACTGTAGGAAGA | 137886 |
rs377062204 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414665 | TAATATAAATTAAAT[G/T]TCTTTGTAGTATTTA | 137886 |
rs377068526 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432541 | GCACCCGCCACCACA[A/C]CCAGCTAATTTTTTG | 137886 |
rs377090250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443341 | ACATCCTTTCCTGCC[A/G]TTTGCCTACAAACCT | 137886 |
rs377101518 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58419268 | TTCCTTTGATTTCAT[A/G]TTCAATATCGAAATT | 137886 |
rs377152205 | snp | C/G | 0.000100548 | 0.0070897 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58430610 | TTCAAAGAGGCAAGG[C/G]AACATGGGGCTGTCC | 137886 |
rs377183764 | snp | A/T | 8.35038e-05 | 0.00646103 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58446036 | GTTAGCAGATGGGAG[A/T]CGTTTGATACAAAGA | 137886 |
rs377333447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424964 | GAATATCAATCACAA[C/T]GTATGTCCCTGTCCG | 137886 |
rs377353928 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421121 | AAGATATTATTAGTT[-/C]TTAAAATCCCCAATA | 137886 |
rs377375346 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437789 | TCATCCTGGCTATGT[A/G]GTAGAGAAGGAGAAA | 137886 |
rs377431889 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425583 | ACCCTCTTTTCGGCC[A/G/T]TAGAGAAGTATGCAC | 137886 |
rs377434938 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448110 | AAACTACAGTTTTGC[C/T]TTGTATTTTACAGAA | 137886 |
rs377483445 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411935 | TTATCAGGTAGGTTT[A/T]TCTTTTAAAGGGGTG | 137886 |
rs377486658 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58429184 | GCCAGATTAGAGATG[C/T]GGAAAGCCTTGAAGG | 137886 |
rs377688705 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441497 | ATGCAGATAAAATGC[C/T]TAGTCATCTCTTCAA | 137886 |
rs386412851 | in-del | -/TT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58432376 | CCTTTCTAAATTTCT[-/TT]TTTTTTTTTTTTTTT | 137886 |
rs386725897 | in-del | A/TTG | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58413134 | GGTAGATGTTGCTAA[A/TTG]TGAGAATGCCTTCAT | 137886 |
rs397966012 | in-del | -/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58423754 | TGGGTTTTTTTTTTT[-/T]AAGCCACTAAAGTTT | 137886 |
rs398007968 | in-del | -/AAAAAAAAAAA | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418256 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAA]TTAATAGTAATTCTG | 137886 |
rs398067858 | in-del | -/AT | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441367 | TATATATATATATAT[-/AT]GTATGTGTATATATA | 137886 |
rs527333162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425030 | TTGCATGCATGATGC[A/G]TTCCTGCTTATGGTG | 137886 |
rs527347509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429176 | TTCACTTTGCCAGAT[A/T]AGAGATGTGGAAAGC | 137886 |
rs527358297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436807 | ATGATTGTAAGTTCC[C/T]TGCGGCTTCACCAGA | 137886 |
rs527440362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437737 | TTGGAACTCATATTT[A/G]AAAGAGAAGCAGAGC | 137886 |
rs527571094 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58416660 | ATTCTAATAGATGTG[G/T]CATTTTGGTTAGTTC | 137886 |
rs527683628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438562 | ACTTCTGTGGGGCCT[C/G]TTGCCTCTTTCTTTT | 137886 |
rs527751273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446207 | AGTTTTTGACAGAAG[A/G]AACATTTTTAAAAGG | 137886 |
rs527815789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58447084 | AATTACAGGCGTAAG[C/T]CACCGTGCCCAGCTG | 137886 |
rs527819072 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437958 | TAAGGCAGCCCCCCC[C/G]CCAACCCCCATCACA | 137886 |
rs527933682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420307 | GAGACAATTAACATC[A/C]ACTAATGTTTCTCTA | 137886 |
rs527973817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445575 | AACTTTACACAGTTG[A/C]CATGGCTGGGATGTG | 137886 |
rs528073354 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443744 | ACTCAGGAGGCAGAG[G/T]TTGCAGTGAGCTGAG | 137886 |
rs528101489 | snp | C/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448195 | TTTTTTTTTTTGATA[C/T]GGAGTTTTGCTCTTG | 137886 |
rs528171859 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446350 | TTTACGTTGTTACTA[A/C]AACTATATGAAGTCG | 137886 |
rs528174435 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423677 | CCTGACCTCATGATC[C/T]GCCAGCCTCGGCCTC | 137886 |
rs528203673 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420916 | GATCCTGACAAAGGC[A/G]TCCTGACATCAGGGA | 137886 |
rs528290916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440981 | CTCTTTACACGTCAG[C/G]CTTCTCTTTCTTTCT | 137886 |
rs528362067 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448779 | CCTTCTTCCTAGACA[C/T]CATTTCATCCTTAAT | 137886 |
rs528461574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427367 | GCTCGGGAGGCTGAA[A/G]TGGCAGGATAGCTTG | 137886 |
rs528515840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422786 | TGGTTCCAAAAACAG[A/G]CTCAGGATTGGCAAA | 137886 |
rs528605896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427028 | ACACATAGTCATCCC[C/T]TGATAAATGTTAGCT | 137886 |
rs528827511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412257 | TTACAACCACACTTC[A/G]TTCTAATGTGAACAA | 137886 |
rs528950200 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58435892 | CATTGTCTCCTTTTT[A/G]TAAGAAATATTTTGT | 137886 |
rs528985711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419664 | TTGGTACTTAGCTGG[A/G]CCTTAAAAGGATTTA | 137886 |
rs528997718 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450391 | TAACGGCAGGACACA[A/G]CTCAGCTTAGCTTTT | 137886 |
rs529067326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58439520 | TTTGTGTTATAATTT[A/G]AGCAAAAAATTCTGT | 137886 |
rs529084740 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448655 | CTAGAATGTCTTCTC[C/T]AGAACAAGACTAGTG | 137886 |
rs529286923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426923 | TCTTCTAATAAGGTT[G/T]TGCCAATTGGCAAGT | 137886 |
rs529313029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421313 | ATAAGTTTCAGGAAG[A/G]CCACACACTAGACAT | 137886 |
rs529339841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440348 | GAGCAATGTGCTTAG[C/T]TTTGTGATTTTCAAT | 137886 |
rs529458095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414825 | ATTTTCCTCATATTC[C/G]TCTTTTCTTAATGTA | 137886 |
rs529564094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414037 | GACGGGGAGGGAGTG[A/G]GAACAGGGATAACTT | 137886 |
rs529592645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422010 | TCTTGTGTGCTGGTG[A/G]AAGACTTTACCCCCA | 137886 |
rs529599099 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58425021 | CGACTGGCCTTGCAT[A/G]CATGATGCGTTCCTG | 137886 |
rs529599840 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58428435 | CATAATTGCATACAA[A/G]GAAAACTGTAAAAGA | 137886 |
rs529765245 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450197 | ATTTGAATAGGCCGC[A/G]AATTTCCCAAATCAT | 137886 |
rs529892209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428222 | GTCGCAGATAATATG[A/T]TTAAGGTTTGGGTAA | 137886 |
rs529900143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422910 | ACTAGCAACTTCTGC[G/T]TTTGCTAATATCCTT | 137886 |
rs529952214 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437729 | ATTTAAAGTTGGAAC[G/T]CATATTTAAAAGAGA | 137886 |
rs529956274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423593 | GGCGCCCGCCACCAC[A/G]CCCTGCTAATTTTTT | 137886 |
rs529959044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435278 | ACATTTCCAAATGTT[G/T]AAATATGTCCAGGAT | 137886 |
rs530009804 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417464 | TCTCTTCTTCCTTTG[A/G]GTGATGATTCCTCTA | 137886 |
rs530068089 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410306 | TAGTCCAAGCTACTC[A/G]GGAGGCTGAGGCAGG | 137886 |
rs530120353 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450955 | ACTCCTTTTCACTTA[C/T]TGAAAACAACTTGGA | 137886 |
rs530214438 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBXN2B | GRCh38.p7 | 8:58435002 | TATTCAGTGCTCTCA[C/T]CCATCCAAAGAACAT | 137886 |
rs530534891 | snp | C/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58426111 | TCTCTTTTAATTGCC[C/G]GTGATGTTCTGTGTA | 137886 |
rs530646696 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440389 | CAGCCAAACCCTTTT[C/T]TCAAGTCATGGAAGT | 137886 |
rs530775061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427381 | AGTGGCAGGATAGCT[A/T]GAGTCCAAGAGGTGG | 137886 |
rs530778259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423521 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 137886 |
rs530778734 | snp | C/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58416005 | AAGGAGCATTTTAAT[C/G]TGTTTTGTTATGATT | 137886 |
rs530779918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441151 | TGCCGAGCGCAGCTC[A/G]TTTTTTTTCATTTTT | 137886 |
rs530842795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442050 | AGATACTAGAACATT[C/G]CATCATCGAAGAAAT | 137886 |
rs531008257 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451443 | ATTTTGCATGATGTA[C/T]GTAATCAAAAAGTTT | 137886 |
rs531100406 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409775 | ACGTTGGCCAGGCTG[G/T]TCTGAAACTCCTGAC | 137886 |
rs531188169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429061 | AAAGATTTCAAATAA[A/T]AAAAACCGTTAACCG | 137886 |
rs531270883 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450777 | ATTTGGAATTCACCT[C/T]TCTCCAGGGTCACTG | 137886 |
rs531380696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424284 | CATAATCTGCAAAAT[A/G]TAGCACACAATTTAA | 137886 |
rs531558218 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441207 | CTATGTTGCCCAGGC[C/T]GGTCTTGAATTCCTG | 137886 |
rs531562534 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58411124 | TGCAAGTCTATGCTG[C/T]CCTCTAGGGCGGCCT | 137886 |
rs531697859 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418554 | ATTAGATTTTTATTA[G/T]AATTTTTGTCGGGTA | 137886 |
rs531714157 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58445240 | ACTAGTAACCAAGTT[C/T]TAATGGTAAGATATT | 137886 |
rs531832732 | snp | C/G | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58411405 | CGGAGGGCGGAGGCC[C/G]TGAGCCCGGCGAGCA | 137886 |
rs531847466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425605 | AGTATGCACTCCTGT[A/T]GTTGTAGTGTCTCAA | 137886 |
rs531917320 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431246 | CCTAGCACTTTGGGA[A/G]GCCGAAGCAGGCAGA | 137886 |
rs531995742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437930 | AAAGCCTTGAAGGCA[G/T]TTCAGAGACCTTTAA | 137886 |
rs532046823 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450644 | TTCCAGCCTCCACCT[A/G]CTGCCCAATTCCAGA | 137886 |
rs532048950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442334 | TTACATAGAACATTT[C/T]ATATTAAAGATTTAC | 137886 |
rs532052204 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433778 | CTGGATCTTTAAGAT[-/A]AAAAAATCAATTAAA | 137886 |
rs532081016 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58411604 | GGATAGAATCCGGCG[C/T]CCGGTCTCCCGATGT | 137886 |
rs532128137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435341 | TCTTTTAGAAGACTA[A/G]TTAGCATGAATTTTG | 137886 |
rs532265281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58435820 | CAATAAGAGTTTTAG[A/C]AAAGACTCTAAAGAA | 137886 |
rs532323171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429021 | CTGGAAGAAAATAGA[A/G]TATCTTTATGACCTT | 137886 |
rs532444286 | in-del | -/G | 0.013683 | 0.0815737 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424689 | TGGAGTACAAGGCGG[-/G]GGGGGGGGGCTCTGA | 137886 |
rs532467721 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423657 | AACCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 137886 |
rs532618990 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414233 | ATCTGTGACCTGGAA[G/T]GCTTGTCAGAGATTG | 137886 |
rs532671232 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451734 | ATGGATTTCTGAAAA[C/G]CTTGTCACAACTGTG | 137886 |
rs532735699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430031 | GGTCTCTTAAATCCA[A/G]AAATCTCTGAAAGAT | 137886 |
rs532752543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419150 | CCTTAAAATATATAG[A/G]TTGAGACGTAAACTG | 137886 |
rs532810667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411526 | GGGCTGGTGACGGCG[C/T]GGGCTGGTGCGAGTT | 137886 |
rs532812504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419510 | CTCAGGATATAGTCT[G/T]ATGCCTGTTTTGACA | 137886 |
rs532823413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445110 | AAATTGAGCTAAATT[C/T]ATTTGAATTATTTAA | 137886 |
rs532887315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445844 | GTTCTAAGTGTTTAT[C/T]GCTGTCTTCAGTTTG | 137886 |
rs533005734 | in-del | -/ATATATATTT | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410784 | TATATATATATATAT[-/ATATATATTT]TTTTTTTTAGTAGAG | 137886 |
rs533022138 | in-del | -/A | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417098 | GAGGCAGATTTGGAT[-/A]AAAAAATAGAAATGA | 137886 |
rs533069544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411979 | CACTCTATGCCCATA[C/T]AGCCTAGTTGTCTAA | 137886 |
rs533152857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431892 | TCTGTATTATTCTTT[C/T]CAAGGAAATATCTCT | 137886 |
rs533185143 | in-del | -/CAT | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431189 | ATTTTATCATGTTAA[-/CAT]GAGTGTTAAACCAGC | 137886 |
rs533263034 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58418296 | GTGATGCCATTTAAT[A/G]TATAGTTAGTAGTCA | 137886 |
rs533293792 | snp | C/T | | | intron-variant, downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58435549 | CACTGGGAAGAGCTG[C/T]GAGCAACTAGGTGGG | 137886 |
rs533301979 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58422209 | CTTTAGGCCACACCC[A/G]TGTTCTGAAGCAATT | 137886 |
rs533469333 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449835 | TGTTCTTCTTTTATA[A/T]TCTCTAAAGCTTTCT | 137886 |
rs533519650 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446407 | ACCTTTTGGGGACTT[A/T]ATTCATTTAAAAATT | 137886 |
rs533604502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423725 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCGGGGAT | 137886 |
rs533699268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426605 | CCTTGCCAAAAAACT[A/G]CTGTCAGCTCCTCTT | 137886 |
rs533747542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445515 | ATTATTCCCTCACTT[G/T]ATAAATGATAGAACT | 137886 |
rs533764408 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410059 | TGTCTCTTTTCCCTA[C/T]TAGACTGAGTTTCAT | 137886 |
rs533908865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417304 | TAAGGGTCTGATGAA[A/G]GCTATAGAATTCTCC | 137886 |
rs534065842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430156 | GCCTTCTTAGGGAGA[A/G]GGGACTATCTTTTGA | 137886 |
rs534113490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411614 | CGGCGCCCGGTCTCC[C/G]GATGTCGGGTCTTGA | 137886 |
rs534178392 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424922 | CAATGTTGCAGTCAA[C/T]ACCTTTCTCTCTGTT | 137886 |
rs534196481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430971 | TTCCCCCAATGGTTC[A/C]CCCCAATGGTTACGT | 137886 |
rs534237031 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58414983 | CCCAATTTAAAATAC[A/G]TCTATCTATATCTAT | 137886 |
rs534255777 | in-del | -/CCCCCAATGGTTC | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430958 | TCACTTCAATGGTTT[-/CCCCCAATGGTTC]CCCCCAATGGTTACG | 137886 |
rs534427194 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413667 | ATCTGAATCAGGAGG[-/GA]GAGTGTTCCAGGTAC | 137886 |
rs534448314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58412428 | TCTTCGGAGAAATAG[A/G]GTATGAATACTTAGC | 137886 |
rs534456074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425301 | TCTCTCCACTTCTTT[C/T]GTTGTCATGACAATC | 137886 |
rs534516150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419300 | TCCCAGTTTCGTTGT[A/G]TTTCTACAGGTCTGT | 137886 |
rs534524741 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442797 | AGGCTTTTGAGCTGG[C/T]GTGTATAATGATAAA | 137886 |
rs534567047 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450679 | CTTTTCTACTTTTAG[G/T]TATTTGTTACAGCAG | 137886 |
rs534633958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425918 | TCACTGGTGCGCACA[A/G]AGAGAACAAAATCTC | 137886 |
rs534689278 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446601 | GTAAGACCCTAATAG[A/T]TATATTTATGATTTT | 137886 |
rs534755226 | snp | A/T | 1.65778e-05 | 0.002879 | missense, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447462 | TTTATTCTTGTGACT[A/T]CATTTCCGAATAAAG | 137886 |
rs534815775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421400 | TTTTTAAAAAAACCC[A/G]ATACCATGTGCCAGA | 137886 |
rs534832385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413332 | AGAACTTGCAAAGAA[A/C]CTTGAAAACAGCCAA | 137886 |
rs534894549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441260 | TGGCCTGCCAAAGTG[C/T]CTGGGTTACAGGCAT | 137886 |
rs534898862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432891 | CCTAGAAACGTGTCT[A/T]TTTAAAAAAGCCTCT | 137886 |
rs534949837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432138 | ATGGATCATGCTTTT[C/G]CTGTATTGTCTAAGA | 137886 |
rs534955567 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449270 | GACATTAACATTTTA[A/C]ATGGAACATTATTCT | 137886 |
rs535015878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440711 | ATGTGATTCCTTCCC[C/T]TCCAAGCCCCCTTCA | 137886 |
rs535028277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449676 | AATTTACAAAACCAG[C/T]GAGGCACCCTTCTTT | 137886 |
rs535115787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446466 | CTGTATAGCAAATAC[C/T]TCATAATATAAATGT | 137886 |
rs535182060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411574 | TCGGCGGAGCCTTTC[C/G]CCGACCCCGTCTGGG | 137886 |
rs535508721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425827 | TTCTCCTCCACCAAC[A/G]TCGTATTTCAGTTCC | 137886 |
rs535569340 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426354 | TGGGACTACAGGTGC[C/G]TGCCACCATGCCCGG | 137886 |
rs535576487 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58447989 | TAATATATACTGAAA[C/T]GTGTCTTTTGATTTT | 137886 |
rs535592400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419942 | TTTGAAATTCTTAAT[G/T]GGTTTTGAACAAGGG | 137886 |
rs535820336 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58448346 | GCCTGGCTAATTTTT[C/G]TACTTTTGCTAGAGA | 137886 |
rs536048688 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449069 | CTGTTTCATCTCTAT[A/G]ACCCTTCTGTTACCA | 137886 |
rs536118436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421637 | TCAGCAACCACCTCT[C/T]TGGAACTTTAATTTC | 137886 |
rs536251894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426764 | CACGTTGGGCTGGCC[C/G]GAGGGAGGCCCGCTC | 137886 |
rs536320303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440654 | ATTGCCACATTGGCA[A/G]TGTTTCCAGTGTATT | 137886 |
rs536390370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58432858 | TCAGGTATTATGGTT[C/G]AATAAATTTGGGATA | 137886 |
rs536437887 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58417749 | AGTAGAGTAAATACT[A/G]TGTTTACTTCACCTA | 137886 |
rs536448096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN2B | GRCh38.p7 | 8:58428709 | GCCCCAAACATTCAT[A/G]AAGAATTAAAGTTGA | 137886 |
rs536475136 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446924 | TGCTCAGCCTCTTGA[A/G]TAGCTGGGATTACAG | 137886 |