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 | 387522 |
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 | 387522 |
rs10268 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50124580 | TGAAGGTGGTGGCTG[A/G]GGCTGTCCACCTGCC | 387522 |
rs15218 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081486 | GTGTGCACAGCAGAT[A/C]CCCGAAATTGGTGGG | 387522 |
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 | 387522 |
rs170825 | snp | A/C | 0.482234 | 0.0925596 | upstream-variant-2KB | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50154354 | CTAATGAAAATGACA[A/C]CTAGGGTCACTATGA | 387522 |
rs189180 | snp | C/T | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135469 | gtttctccatgttgg[C/T]caggctggtctcaaa | 387522 |
rs232732 | snp | C/T | 0.483418 | 0.0895317 | upstream-variant-2KB | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50155092 | gacagagggagactc[C/T]gtctcaaaaaaaaaa | 387522 |
rs232733 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50153622 | GCTGGCCCGGCCAGT[C/T]CTCGGCGCCCGCCAT | 387522 |
rs232734 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50150314 | TAATCTCAAACATTC[C/T]GCTCCTAGAACCCAG | 387522 |
rs232735 | snp | C/G | 0.498392 | 0.028309 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50147850 | ACGAGGTCAAGAGTT[C/G]GAGATCAGCCTGGCT | 387522 |
rs232736 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50147758 | ATTCTCATCCATAAA[A/G]AATGCATACACAATG | 387522 |
rs232737 | snp | C/G | 0.480697 | 0.0963277 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50147496 | TTCAAGTATCAGCCC[C/G]TCAAGGAAGGAACTG | 387522 |
rs232738 | snp | A/G | 0.464947 | 0.127663 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50139019 | AAGGCGTGGCTGAGG[A/G]GCCAAGTGAATGCAC | 387522 |
rs232739 | snp | A/G | 0.466515 | 0.124985 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50138474 | GGCCCGGTGGGTCCC[A/G]CGACACAGCAAGCAT | 387522 |
rs232740 | snp | A/C | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135527 | gggattacaggcatg[A/C]gccaccacacctggc | 387522 |
rs232741 | snp | C/T | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135497 | ctaattttgtatttt[C/T]agtagagacagggtt | 387522 |
rs232742 | snp | A/T | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135479 | tagagacagggtttc[A/T]ccatgttggtcaggc | 387522 |
rs232743 | snp | C/T | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135439 | actcctgacctcagg[C/T]gatccgcttgcctcg | 387522 |
rs232744 | snp | A/G | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135398 | gtgctagaattacag[A/G]tgtgagccaccgtgc | 387522 |
rs232745 | snp | A/G | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50135386 | cagatgtgagccacc[A/G]tgcccggccTGGAAA | 387522 |
rs232746 | snp | C/T | 0.423413 | 0.180077 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50134525 | gcactccaggctagg[C/T]aacaagagcaaaact | 387522 |
rs232747 | snp | A/G | 0.465473 | 0.126772 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50134440 | taatcccagctactc[A/G]ggaggctgaggcagg | 387522 |
rs232748 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50123891 | gcctggcacacacca[C/G]gtgccagtgaatatt | 387522 |
rs365088 | snp | A/T | 0.423257 | 0.180228 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50136100 | atcaggttttttttT[A/T]TAAAAAAAGTAGTTG | 387522 |
rs365089 | snp | A/T | 0.428937 | 0.17459 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50136099 | tcaggttttttttTT[A/T]AAAAAAAGTAGTTGA | 387522 |
rs367033 | snp | G/T | 0.100231 | 0.200173 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116630 | ATTCCAGTCGCCATG[G/T]CCCCACATGGCAAGG | 387522 |
rs383495 | snp | C/T | 0.421842 | 0.181577 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50113494 | CTGTCTAGTTCCTAT[C/T]TAGATCCTCACCACA | 387522 |
rs742590 | snp | C/G | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50134967 | tcaaactcctgacct[C/G]cagtggtccgcctgc | 387522 |
rs761213 | snp | C/G | 0.46845 | 0.121572 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50133602 | TCCAGAAGCCCTTCT[C/G]GGGCTTCCACCTCCC | 387522 |
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 | 387522 |
rs926603 | snp | G/T | 0 | 0 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50132829 | GTGGAGTGTGGCTTA[G/T]TTGATTGACTCAATG | 387522 |
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 | 387522 |
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 | 387522 |
rs1883687 | snp | C/T | 0.461923 | 0.132621 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50105701 | CACCTGTAATCTCAG[C/T]ACTTTGAGAGGCCGA | 387522 |
rs1883688 | snp | C/T | 0.180702 | 0.240204 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50105846 | GAGGCATGACAATCA[C/T]TTGAACCCGGGAGGT | 387522 |
rs1928544 | snp | C/T | 0.384401 | 0.210799 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117213 | GATACAGGAAGCTGA[C/T]GCAGTGGTTCGGTTG | 387522 |
rs1928545 | snp | C/T | 0.378174 | 0.214642 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117266 | TCCACAATGTCCATT[C/T]GTGAACTCTCTTTTC | 387522 |
rs1928546 | snp | A/G | 0.378174 | 0.214642 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50117482 | GAAAGTAAAGCTGAC[A/G]AACTGTCGACAGGAA | 387522 |
rs1980925 | snp | A/G | 0.414905 | 0.187899 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50132435 | TCTCCTTTCCCTTGC[A/G]tgcctctgggtcttt | 387522 |
rs2013393 | snp | C/T | 0.234109 | 0.249494 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50084990 | AGAGTCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 387522 |
rs2026757 | snp | A/C | 0.104326 | 0.203173 | missense, nc-transcript-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50153619 | GCTGCTGGCCCGGCC[A/C]GTCCTCGGCGCCCGC | 387522 |
rs2026758 | snp | A/T | 0.483199 | 0.0901004 | upstream-variant-2KB | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50154031 | GCAATGGGCCGAGGC[A/T]GGGCCCAGAAATGGG | 387522 |
rs2026759 | snp | C/G | 0.483053 | 0.0904792 | upstream-variant-2KB | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50154178 | AGCGAGGCCGATGGA[C/G]AGTGGGCTGGTTTAT | 387522 |
rs2073053 | snp | G/T | 0.259951 | 0.249802 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50083259 | CACATCTGTCCCCCT[G/T]ACCTGGGCGCAGTGA | 387522 |
rs2179600 | snp | A/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092469 | TGCAATGGAGACGGG[A/G]GTACTGCTGGCTTCT | 387522 |
rs2269214 | snp | A/G | 0.458315 | 0.13822 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108761 | TATTTTATACTGAAT[A/G]ACTCACACCTCTTGG | 387522 |
rs2269215 | snp | G/T | 0.457853 | 0.138915 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108724 | AGCCCCATCATGGCA[G/T]GTACAAAGTAGTACC | 387522 |
rs2269216 | snp | A/T | 0.471768 | 0.115407 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50108711 | CAGGTACAAAGTAGT[A/T]CCTCATCCTTATTTA | 387522 |
rs2269217 | snp | C/G | 0.362523 | 0.223246 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50089858 | TGAAGGGTCAAATGC[C/G]TCCTACTTTTTATTT | 387522 |
rs2269218 | snp | C/T | 0.361684 | 0.223667 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50089628 | GCAGAGAGGTGCCTG[C/T]TGCTGCTGGCTAGGA | 387522 |
rs2301018 | snp | A/G | 0.461592 | 0.133149 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091644 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 387522 |
rs2301019 | snp | A/G | 0.460365 | 0.13508 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091193 | tgggcgtagtgatgc[A/G]cgcctgtagtcccag | 387522 |
rs2301020 | snp | C/T | 0.471004 | 0.116864 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087982 | GTGCACACAAATATA[C/T]CCAGAATTGGAAGAA | 387522 |
rs2301021 | snp | A/G | 0.361474 | 0.223771 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50087758 | GTAGTTATTTTTGCT[A/G]TTGCAGACAGTGCTT | 387522 |
rs2664532 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081244 | GATGTTAAATCCTTA[A/G]AACTAAGGTTTTCCC | 387522 |
rs2664558 | snp | A/G | 0.410061 | 0.192043 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50124008 | CTCCAAAAGGCTTTG[A/G]AGCAGATGTCAACAT | 387522 |
rs2664563 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50081324 | TGCTGCTTCAAAAGG[G/T]GGTTTTACACAAATA | 387522 |
rs2869953 | snp | A/T | 0.5 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094010 | aaaaaaaaaaaaaaa[A/T]aataataataataat | 387522 |
rs2869954 | snp | A/C | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094033 | ataataataataata[A/C]Aatatatatatataa | 387522 |
rs2869955 | snp | C/T | 0.422473 | 0.180978 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50103142 | atgagagtaaaactt[C/T]atctgttttgttcac | 387522 |
rs2869956 | snp | A/T | 0.471388 | 0.116136 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106412 | ACAGCAACATATTAA[A/T]ATATTTGTGGTACAA | 387522 |
rs2869957 | snp | A/G | 0.374 | 0.217081 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50115960 | GAGGTTAGGCGGGAC[A/G]GCCCGAGGCATGCTG | 387522 |
rs2869958 | snp | C/T | 0.471196 | 0.1165 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50140226 | catcaccacctccac[C/T]gctccacccaggtct | 387522 |
rs2904252 | snp | C/G | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50112921 | GGCCCCTCAGCCCCC[C/G]GCCCGTGCTTCCGGC | 387522 |
rs3067702 | in-del | -/ATAT | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094041 | aataataaaatatat[-/ATAT]ataaAatatattatg | 387522 |
rs3067703 | in-del | -/TATAT | 0.420733 | 0.18262 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094124 | aataaaaatatatta[-/TATAT]tataattatatatct | 387522 |
rs3091898 | in-del | -/CTA | 0.480697 | 0.0963277 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50147891 | GGTGAAACCCCGTCT[-/CTA]CTAAGAATACAAAAA | 387522 |
rs3091914 | in-del | -/C/CC | 0 | 0 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50142695 | CGCCCCCCCCCCCCC[-/C/CC]GCCCCAACGGCCTCC | 387522 |
rs3092037 | in-del | -/A | 0.128976 | 0.218754 | intron-variant | TMEM189-UBE2V1 | GRCh38.p7 | 20:50120101 | CGAGACCCCATCTCT[-/A]AAAAAAAAAAAAAAT | 387522 |
rs3092440 | in-del | -/G | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50147350 | CCCCCATCCAATGGG[-/G]ATATGAGCTCCAGGT | 387522 |
rs3746559 | snp | A/G | 0.422158 | 0.181278 | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50141654 | TAACCATCCCCAGAT[A/G]AGGCTGCAAAGCTCA | 387522 |
rs3819905 | snp | C/T | 0.431473 | 0.171952 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092210 | CTCAGCCTCCCTAGT[C/T]GCTGGGGTTATAGGC | 387522 |
rs5841791 | in-del | -/C | 0.10237 | 0.201756 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106711 | GCGCATGCCTGTAAT[-/C]CGAGCTACTCAGGGG | 387522 |
rs6012829 | snp | C/G | 0.460365 | 0.13508 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088679 | TGGTCTTGGCTACTT[C/G]GGAGGCTGAGGCAGG | 387522 |
rs6012830 | snp | C/G | 0 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50092355 | CTATTTTGGAGAACC[C/G]CAGAGGCTCAAcagt | 387522 |
rs6012831 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50096512 | AAACAGCATCAGAGG[A/G]GGTTCAAATATATAA | 387522 |
rs6012833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50097750 | GTTTCAAGTTCTCTG[A/C]CTTGAATGCTGAGCT | 387522 |
rs6012834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50097893 | AAGTGTAGGACACAC[A/G]CCattaattcaattg | 387522 |
rs6012835 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50103647 | ctggcctcaagtgat[C/G]tgcccgccttggcct | 387522 |
rs6012836 | snp | A/C | | | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106887 | aacaaaaaaaaaaaa[A/C]caaaaaaaaGGTAGA | 387522 |
rs6012837 | snp | A/C | 0.5 | 0 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50106888 | ACAAAAAAAAAAAAA[A/C]AAAAAAAAGGTAGAA | 387522 |
rs6012838 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50110615 | CCTGCACTCTTTTCA[A/C]TGCCTAGGGACGAAG | 387522 |
rs6012839 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50110617 | TGCACTCTTTTCACT[C/G]CCTAGGGACGAAGGT | 387522 |
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 | 387522 |
rs6012842 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116080 | CTGGACGTCACAGCC[A/G]GTCCCCAGAGCAGGA | 387522 |
rs6012843 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB, intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50116092 | GCCGGTCCCCAGAGC[A/G]GGATTCCTTCCGGCG | 387522 |
rs6012845 | snp | C/T | 0.467439 | 0.123371 | intron-variant | TMEM189-UBE2V1 | GRCh38.p7 | 20:50118793 | cccagctaattattt[C/T]ttttgtatttttggt | 387522 |
rs6012846 | snp | C/T | 0.47517 | 0.10862 | intron-variant | TMEM189-UBE2V1 | GRCh38.p7 | 20:50120977 | CGGTTGAGCTGGAAA[C/T]CCATGTTTGCCCTGC | 387522 |
rs6012851 | snp | C/T | | | intron-variant | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50151655 | acaaggtcaagagat[C/T]gagaccaccctggct | 387522 |
rs6012852 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | TMEM189, TMEM189-UBE2V1 | GRCh38.p7 | 20:50155190 | ggccagtggatcacc[C/T]aaggccaggagtttg | 387522 |
rs6020245 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088524 | ggcacggtggcccac[A/G]cctgtaatctcagca | 387522 |
rs6020246 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50088750 | gtgattgtgtcactg[A/C]acttcagcctgggtg | 387522 |
rs6020247 | snp | C/T | 0.45843 | 0.138046 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091019 | CGGGACTAAGTTAAC[C/T]TCTTATTCTATATAC | 387522 |
rs6020248 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091142 | acctctgcctcctgg[A/G]ttcaagcgattctcc | 387522 |
rs6020250 | snp | C/T | 0.458545 | 0.137872 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50091297 | GTGATTCACCTGCCT[C/T]GGCCTCCCAAAGCGC | 387522 |
rs6020255 | snp | C/T | 0.471768 | 0.115407 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094849 | GACCACCGAACTGTA[C/T]ATTTAAAAGGGTGAA | 387522 |
rs6020256 | snp | C/T | 0.457504 | 0.139435 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50094888 | CAATAAAGCTGTTAC[C/T]AAAAACAAATACATG | 387522 |
rs6020257 | snp | G/T | 0.457504 | 0.139435 | intron-variant, downstream-variant-500B | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50095033 | GCAGAATTTACTGAT[G/T]CATTGTTTTGTGTGT | 387522 |
rs6020260 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE2V1, TMEM189-UBE2V1 | GRCh38.p7 | 20:50099081 | TCCTAATTAGGCTAG[C/T]GGGGGAAAAGTCACT | 387522 |