SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2733 | snp | A/G | 0.1472 | 0.227886 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081535 | CTGCTGAGGATCTTG[A/G]GAAGCAGCAGCAGCA | 7335 |
rs8585 | snp | C/T | 0.465473 | 0.126772 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50082386 | TCTCTGCCTTCTCCC[C/T]TTACCCTCCCGCCTC | 7335 |
rs15218 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081486 | GTGTGCACAGCAGAT[A/C]CCCGAAATTGGTGGG | 7335 |
rs126907 | snp | C/G | 0.132525 | 0.22068 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113140 | CCGGCCTTCAAGCAA[C/G]AGCGACGCAAGATGG | 7335 |
rs367033 | snp | G/T | 0.100231 | 0.200173 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116630 | ATTCCAGTCGCCATG[G/T]CCCCACATGGCAAGG | 7335 |
rs383495 | snp | C/T | 0.421842 | 0.181577 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113494 | CTGTCTAGTTCCTAT[C/T]TAGATCCTCACCACA | 7335 |
rs761214 | snp | A/G | 0.405396 | 0.199424 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113174 | CCGGGGGACGGGTAA[A/G]GGGGGGGTGAAGAAG | 7335 |
rs1049679 | snp | C/T | 0.27893 | 0.24832 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50082246 | CCTGCACCCCTGGTT[C/T]CTTTAAGTCTTAAGT | 7335 |
rs1049871 | snp | A/T | 0.321769 | 0.239477 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081254 | TTTTTCTGGGGGGAA[A/T]ACCTTAGTTCTAAGG | 7335 |
rs1883687 | snp | C/T | 0.461923 | 0.132621 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50105701 | CACCTGTAATCTCAG[C/T]ACTTTGAGAGGCCGA | 7335 |
rs1883688 | snp | C/T | 0.180702 | 0.240204 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50105846 | GAGGCATGACAATCA[C/T]TTGAACCCGGGAGGT | 7335 |
rs1928544 | snp | C/T | 0.384401 | 0.210799 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117213 | GATACAGGAAGCTGA[C/T]GCAGTGGTTCGGTTG | 7335 |
rs1928545 | snp | C/T | 0.378174 | 0.214642 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117266 | TCCACAATGTCCATT[C/T]GTGAACTCTCTTTTC | 7335 |
rs1928546 | snp | A/G | 0.378174 | 0.214642 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117482 | GAAAGTAAAGCTGAC[A/G]AACTGTCGACAGGAA | 7335 |
rs2013393 | snp | C/T | 0.234109 | 0.249494 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50084990 | AGAGTCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 7335 |
rs2073053 | snp | G/T | 0.259951 | 0.249802 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50083259 | CACATCTGTCCCCCT[G/T]ACCTGGGCGCAGTGA | 7335 |
rs2179600 | snp | A/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092469 | TGCAATGGAGACGGG[A/G]GTACTGCTGGCTTCT | 7335 |
rs2269214 | snp | A/G | 0.458315 | 0.13822 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108761 | TATTTTATACTGAAT[A/G]ACTCACACCTCTTGG | 7335 |
rs2269215 | snp | G/T | 0.457853 | 0.138915 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108724 | AGCCCCATCATGGCA[G/T]GTACAAAGTAGTACC | 7335 |
rs2269216 | snp | A/T | 0.471768 | 0.115407 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108711 | CAGGTACAAAGTAGT[A/T]CCTCATCCTTATTTA | 7335 |
rs2269217 | snp | C/G | 0.362523 | 0.223246 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50089858 | TGAAGGGTCAAATGC[C/G]TCCTACTTTTTATTT | 7335 |
rs2269218 | snp | C/T | 0.361684 | 0.223667 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50089628 | GCAGAGAGGTGCCTG[C/T]TGCTGCTGGCTAGGA | 7335 |
rs2301018 | snp | A/G | 0.461592 | 0.133149 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091644 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 7335 |
rs2301019 | snp | A/G | 0.460365 | 0.13508 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091193 | tgggcgtagtgatgc[A/G]cgcctgtagtcccag | 7335 |
rs2301020 | snp | C/T | 0.471004 | 0.116864 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087982 | GTGCACACAAATATA[C/T]CCAGAATTGGAAGAA | 7335 |
rs2301021 | snp | A/G | 0.361474 | 0.223771 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087758 | GTAGTTATTTTTGCT[A/G]TTGCAGACAGTGCTT | 7335 |
rs2664532 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081244 | GATGTTAAATCCTTA[A/G]AACTAAGGTTTTCCC | 7335 |
rs2664563 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081324 | TGCTGCTTCAAAAGG[G/T]GGTTTTACACAAATA | 7335 |
rs2869953 | snp | A/T | 0.5 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094010 | aaaaaaaaaaaaaaa[A/T]aataataataataat | 7335 |
rs2869954 | snp | A/C | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094033 | ataataataataata[A/C]Aatatatatatataa | 7335 |
rs2869955 | snp | C/T | 0.422473 | 0.180978 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50103142 | atgagagtaaaactt[C/T]atctgttttgttcac | 7335 |
rs2869956 | snp | A/T | 0.471388 | 0.116136 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106412 | ACAGCAACATATTAA[A/T]ATATTTGTGGTACAA | 7335 |
rs2869957 | snp | A/G | 0.374 | 0.217081 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50115960 | GAGGTTAGGCGGGAC[A/G]GCCCGAGGCATGCTG | 7335 |
rs2904252 | snp | C/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50112921 | GGCCCCTCAGCCCCC[C/G]GCCCGTGCTTCCGGC | 7335 |
rs3067702 | in-del | -/ATAT | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094041 | aataataaaatatat[-/ATAT]ataaAatatattatg | 7335 |
rs3067703 | in-del | -/TATAT | 0.420733 | 0.18262 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094124 | aataaaaatatatta[-/TATAT]tataattatatatct | 7335 |
rs3819905 | snp | C/T | 0.431473 | 0.171952 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092210 | CTCAGCCTCCCTAGT[C/T]GCTGGGGTTATAGGC | 7335 |
rs5841791 | in-del | -/C | 0.10237 | 0.201756 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106711 | GCGCATGCCTGTAAT[-/C]CGAGCTACTCAGGGG | 7335 |
rs6012829 | snp | C/G | 0.460365 | 0.13508 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088679 | TGGTCTTGGCTACTT[C/G]GGAGGCTGAGGCAGG | 7335 |
rs6012830 | snp | C/G | 0 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092355 | CTATTTTGGAGAACC[C/G]CAGAGGCTCAAcagt | 7335 |
rs6012831 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50096512 | AAACAGCATCAGAGG[A/G]GGTTCAAATATATAA | 7335 |
rs6012833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50097750 | GTTTCAAGTTCTCTG[A/C]CTTGAATGCTGAGCT | 7335 |
rs6012834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50097893 | AAGTGTAGGACACAC[A/G]CCattaattcaattg | 7335 |
rs6012835 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50103647 | ctggcctcaagtgat[C/G]tgcccgccttggcct | 7335 |
rs6012836 | snp | A/C | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106887 | aacaaaaaaaaaaaa[A/C]caaaaaaaaGGTAGA | 7335 |
rs6012837 | snp | A/C | 0.5 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106888 | ACAAAAAAAAAAAAA[A/C]AAAAAAAAGGTAGAA | 7335 |
rs6012838 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50110615 | CCTGCACTCTTTTCA[A/C]TGCCTAGGGACGAAG | 7335 |
rs6012839 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50110617 | TGCACTCTTTTCACT[C/G]CCTAGGGACGAAGGT | 7335 |
rs6012840 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50111443 | TCGTTTATTACGACC[C/T]GGTAGGAGTGTTATT | 7335 |
rs6012842 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116080 | CTGGACGTCACAGCC[A/G]GTCCCCAGAGCAGGA | 7335 |
rs6012843 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116092 | GCCGGTCCCCAGAGC[A/G]GGATTCCTTCCGGCG | 7335 |
rs6020245 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088524 | ggcacggtggcccac[A/G]cctgtaatctcagca | 7335 |
rs6020246 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088750 | gtgattgtgtcactg[A/C]acttcagcctgggtg | 7335 |
rs6020247 | snp | C/T | 0.45843 | 0.138046 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091019 | CGGGACTAAGTTAAC[C/T]TCTTATTCTATATAC | 7335 |
rs6020248 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091142 | acctctgcctcctgg[A/G]ttcaagcgattctcc | 7335 |
rs6020250 | snp | C/T | 0.458545 | 0.137872 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091297 | GTGATTCACCTGCCT[C/T]GGCCTCCCAAAGCGC | 7335 |
rs6020255 | snp | C/T | 0.471768 | 0.115407 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094849 | GACCACCGAACTGTA[C/T]ATTTAAAAGGGTGAA | 7335 |
rs6020256 | snp | C/T | 0.457504 | 0.139435 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094888 | CAATAAAGCTGTTAC[C/T]AAAAACAAATACATG | 7335 |
rs6020257 | snp | G/T | 0.457504 | 0.139435 | intron-variant, downstream-variant-500B | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50095033 | GCAGAATTTACTGAT[G/T]CATTGTTTTGTGTGT | 7335 |
rs6020260 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50099081 | TCCTAATTAGGCTAG[C/T]GGGGGAAAAGTCACT | 7335 |
rs6020261 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50099654 | ggctccttcccctag[A/G]aatccataagccaag | 7335 |
rs6020262 | snp | C/T | 0.4582 | 0.138394 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50101012 | CAACATACATTTCTA[C/T]TGGATTAGATATTCG | 7335 |
rs6020263 | snp | A/G | 0.45866 | 0.137698 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50101512 | CAACCTCTGCCTCCT[A/G]GGTTCAAGCAATTCT | 7335 |
rs6020264 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50102681 | acaggtgtgagccac[C/T]gtgctcggccGACGA | 7335 |
rs6020266 | snp | C/T | 0.45866 | 0.137698 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50104150 | agctgggcgtggtgg[C/T]gcgcgcctgtaatcc | 7335 |
rs6020267 | snp | G/T | 0.45866 | 0.137698 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50104244 | CCGAGATCGCGCCAC[G/T]GCACTCCAGCCTGGC | 7335 |
rs6020271 | snp | A/G | 0.492337 | 0.0614248 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50114937 | GGGGCGTGGTAGCAC[A/G]CACCTGTAATCCCAG | 7335 |
rs6020275 | snp | C/T | 0.0283406 | 0.115616 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117803 | gcattgcactccagg[C/T]tgggcaacaaagcga | 7335 |
rs6063471 | snp | C/T | 0 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50100842 | AGGTTACCTTTTCAC[C/T]TAACAATCAGATCTG | 7335 |
rs6067346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088227 | tgtcattgccacgag[A/G]agccagagatatgat | 7335 |
rs6067348 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092058 | gggtgtggtgggctc[A/G]tgcctgtaatcccag | 7335 |
rs6091097 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113855 | tatgtaccagacact[C/G]tgctaggcgctgggg | 7335 |
rs6095755 | snp | G/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50082092 | TCGATAAAGGTGGGG[G/T]AGAGAAGATATGGGG | 7335 |
rs6095756 | snp | G/T | 0.462909 | 0.131034 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50086943 | TTAGCCGGGTGTGGT[G/T]GTGGGCGCCTATAGT | 7335 |
rs6095757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087928 | GGTATAGACGATACA[C/T]TGTAGGATATGTATA | 7335 |
rs6095760 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50096067 | TGTGTCCTCAAAAAA[C/T]GGTTGGCTGGCATTA | 7335 |
rs6095763 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50103333 | ACAAGAGAGAAACAT[C/T]CACAGCACCATTATC | 7335 |
rs6095765 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50109148 | AACATCACAGGTAAG[C/T]CGAAGTCTATGGGAC | 7335 |
rs6095768 | snp | C/T | 0.458545 | 0.137872 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50111064 | TTGAATGGAAGCTCC[C/T]GAAGGATACAGACTA | 7335 |
rs6095769 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50114516 | TCTGGATAAAATACA[A/C]ACTTTACAAGTTGAG | 7335 |
rs6095771 | snp | A/G | 0.00146252 | 0.0270023 | missense, utr-variant-5-prime, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50115572 | cttgaacctctcctg[A/G]catcagtttcccctt | 7335 |
rs6122872 | snp | G/T | 0.122411 | 0.214991 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50101024 | CTACTGGATTAGATA[G/T]TCGATTACTTAAAAA | 7335 |
rs6125888 | snp | G/T | 0.200801 | 0.245111 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50083114 | TTCCCTTTTGTGCCC[G/T]GAACCATTACTATCT | 7335 |
rs6125890 | snp | A/G | 0.42574 | 0.177808 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087433 | GCTAGACTTTAATAG[A/G]AACCAGGGTTACAGG | 7335 |
rs6125891 | snp | A/G | 0.425277 | 0.178263 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091463 | GTTGCAAGCAGTGGC[A/G]CGATCTCGGCTTACT | 7335 |
rs6125892 | snp | A/T | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50093991 | AGACTCCAACTCAAA[A/T]AAAAAAAAAAAAAAA | 7335 |
rs6125893 | snp | A/T | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50093992 | GACTCCAACTCAAAA[A/T]AAAAAAAAAAAAAAA | 7335 |
rs6125898 | snp | A/G | 0.421526 | 0.181876 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50101027 | CTGGATTAGATATTC[A/G]ATTACTTAAAAACAA | 7335 |
rs6125903 | snp | C/T | 0.422315 | 0.181128 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106690 | ACAAAATTAGCTGGG[C/T]GTGGTGGCGCATGCC | 7335 |
rs6125904 | snp | A/C | 0.419776 | 0.18351 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106848 | TTCAAAACCAAAAAC[A/C]ACAACAACAACAACA | 7335 |
rs6125905 | snp | C/T | 0.422 | 0.181428 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50109998 | CTCTGGGGAAGACTC[C/T]TGAATGGAAGGGAAG | 7335 |
rs6125906 | snp | A/C | 0.108402 | 0.206034 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113266 | TGCACGACCCGTGGC[A/C]TGGAAGGCTCTTTTC | 7335 |
rs6125907 | snp | A/C | 0.109461 | 0.206758 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113778 | CCCAATTCATTCATT[A/C]ATTCATTCATTCATT | 7335 |
rs7261304 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092515 | gggatgctgctaaac[A/G]gcctacaacgcacat | 7335 |
rs7261793 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117369 | TCAAAAGGTGAAAAA[A/C]CAAAAATTATATAAT | 7335 |
rs7261847 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117370 | CAAAAGGTGAAAAAA[A/C]AAAAATTATATAATG | 7335 |
rs7263046 | snp | C/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092706 | GGAGCAGTTGGCTCA[C/G]AAGCTTTGTTTTTAG | 7335 |
rs7270646 | snp | A/T | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092698 | TTGTGCAAGGAGCAG[A/T]TGGCTCAGAAGCTTT | 7335 |
rs7273529 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50090901 | tcatcacactgtata[C/T]cttggatatatacag | 7335 |
rs7362075 | snp | A/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50083057 | ATACCTTACATGCGG[A/G]ATACCTACCTGCTAG | 7335 |