SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3365 | snp | G/T | 0.163246 | 0.234465 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683164 | TAAGGCCTAAGGAAT[G/T]AGGGGCAGGGGGCGA | 9866 |
rs885114 | snp | A/G | 0.488726 | 0.0742286 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657209 | TAGGCCACCAAGTGA[A/G]GACACACTCGTTGCA | 9866 |
rs1128559 | snp | C/G | 0.330249 | 0.23677 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615644 | GAGAGGCTCCCTTTA[C/G]ACACCTGCCTCTCGC | 9866 |
rs1502316 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662504 | TAACTACCATAGCCC[A/G]ATGCTTCTTGAAGCT | 9866 |
rs1502317 | snp | A/G | 0.494187 | 0.0535994 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660471 | AAGAACAGGCAGTCT[A/G]TGGTTTTCTGACCCC | 9866 |
rs1875568 | snp | C/T | 0.480223 | 0.0974544 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678620 | ATTGGGATTTCTGAG[C/T]TTTTCTCTAATTCTC | 9866 |
rs2036423 | snp | C/T | 0.490618 | 0.0678448 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677678 | GTTCTTTCCATTAAT[C/T]TTATCCTCTGAAATT | 9866 |
rs2073684 | snp | C/T | 0.322007 | 0.239405 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683418 | CGATCCTCTAGTATT[C/T]CAGTTCTAAGGAATT | 9866 |
rs2316901 | snp | C/T | 0.499154 | 0.0205497 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657469 | AAGCTCCTCCCTGTC[C/T]CAGGGCCTCCATGTC | 9866 |
rs3942866 | snp | C/T | 0.370974 | 0.218781 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676781 | CCTGACCTAGAAGAG[C/T]GTAGGGGACAGAGTT | 9866 |
rs4256980 | snp | C/G | 0.49941 | 0.0171624 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652392 | TTAGTCAGAGAAAGG[C/G]AAGGCCTCCCTGCCC | 9866 |
rs4258378 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8652903 | TCCAAAATACCAGGc[C/T]taccagccaatgacc | 9866 |
rs4272783 | snp | C/T | 0.485049 | 0.0851591 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663846 | tggttgtacttacag[C/T]acattgtaagtgaaa | 9866 |
rs4291677 | snp | C/T | 0.489083 | 0.0730708 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8659344 | CAGGGTAGTTGAGCA[C/T]TAATGGGACCCTAAA | 9866 |
rs4495896 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666158 | cctggccaatatggc[A/G]aaaccccatctctac | 9866 |
rs4503528 | snp | A/G | 0.487809 | 0.0771174 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8642907 | CACTGGCAGTCCCAG[A/G]GAGTGCTTTCTCTTG | 9866 |
rs4511283 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644843 | CTTCTTTCAGAAGAT[A/G]GCCTGATTCCCAGAT | 9866 |
rs4520599 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678611 | CTGAAGTAAATTGGG[A/G]TTTCTGAGCTTTTCT | 9866 |
rs4929923 | snp | C/T | 0.497829 | 0.0328757 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617653 | CCAAGGAAAGTAGGT[C/T]TTCCCGAGCCTAACC | 9866 |
rs4929924 | snp | A/G | 0.499741 | 0.0113788 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617778 | TAGTGGATGTACTAC[A/G]GCTCCCAAATAAATG | 9866 |
rs4929925 | snp | A/C | 0.499234 | 0.0195537 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633640 | CGGGAACATTCTGAG[A/C]AAATGCTGCTGTCAG | 9866 |
rs4929926 | snp | C/T | 0.49925 | 0.0193545 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636829 | ACTCCTCACATCCCC[C/T]AAGACTGAATCCCAG | 9866 |
rs4929927 | snp | A/G | 0.49925 | 0.0193545 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636938 | ATCAAGCCAAATTAC[A/G]AATTATCTGAAGCCC | 9866 |
rs4929928 | snp | C/T | 0.499897 | 0.00718776 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653539 | CCCCAACTAACCCAC[C/T]AGCTGAATACAGTGC | 9866 |
rs4929947 | snp | C/G | 0.499977 | 0.00339449 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618447 | CACAATCACAGTGTG[C/G]AGTAACCAGCACCAA | 9866 |
rs4929948 | snp | G/T | 0.499325 | 0.0183582 | intron-variant | TRIM66 | GRCh38.p7 | 11:8622983 | CTTTGGCCACACATC[G/T]GTCATACAGTAGTTA | 9866 |
rs4929951 | snp | A/G | 0.00739983 | 0.0603751 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640521 | tggctgctgtggggg[A/G]gggggaaggggaggt | 9866 |
rs6486253 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646803 | ACCAAGGTCAACCCA[A/G]TAGCCCACCAGTTGA | 9866 |
rs7101911 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670264 | atgattcgctgcctt[G/T]gcctcccaaagtgct | 9866 |
rs7106264 | snp | A/C | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665300 | TAGGCTAGCCAGAGA[A/C]AGGTGACAGCTCTGC | 9866 |
rs7106755 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648784 | CCCAAGCATCCCACT[A/G]CCTGCCAGAGGCTGA | 9866 |
rs7107276 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636053 | CCCCTTGCCTTTCCC[G/T]TAATCATTCCTGGGC | 9866 |
rs7110529 | snp | C/G | 0.460589 | 0.13473 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666163 | ccaatatggcgaaac[C/G]ccatctctactaaaa | 9866 |
rs7110534 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8666170 | ggcgaaaccccatct[C/T]tactaaaaatacaaa | 9866 |
rs7113874 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666469 | TTTTTTCCCCTATTT[C/T]ACATGTTCTCAAGTT | 9866 |
rs7114215 | snp | A/T | 0.116138 | 0.211142 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670019 | tttgtttttatttat[A/T]tttttttttttgaga | 9866 |
rs7118611 | snp | A/C | 0.461037 | 0.134028 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664138 | atgtaaagtgttctc[A/C]ccaccaaaatgataa | 9866 |
rs7118686 | snp | G/T | 0.0659589 | 0.169201 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673925 | TTCAGGAAGGAGGAA[G/T]GGTGATGGGGCTGGG | 9866 |
rs7121168 | snp | A/C | 0.103082 | 0.202275 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673452 | TCTCAGGTTAATGAG[A/C]TGAGAGAGGGGCAGA | 9866 |
rs7122232 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674443 | ggctggagggcagtc[A/G]tgcgaagttcactgc | 9866 |
rs7123627 | snp | A/T | 0.100231 | 0.200173 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652502 | GCTCTCTCCCCATAG[A/T]CCAAGTTAGATGCAT | 9866 |
rs7123873 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652653 | ACTCCCACCCTGGAG[A/T]CCACAGTGATTCTGC | 9866 |
rs7126235 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667789 | attatatgtatatac[C/T]acattttgtttatcc | 9866 |
rs7130096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677353 | TGCCTGGCACCTAGC[A/G]TAGGAACATAGTACA | 9866 |
rs7930642 | snp | C/G | 0.0376037 | 0.131863 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653519 | ggccatcatagacca[C/G]ccagccccaactaac | 9866 |
rs7933556 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664101 | taatatattgtattc[C/T]tgaaagatgccaaga | 9866 |
rs7933614 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627145 | TCTGTTTCCCCTACT[A/G]AAGTGTAAACTCCAT | 9866 |
rs7934978 | snp | C/T | 0.266819 | 0.249434 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641551 | GCAAAGGGTAGAGAG[C/T]CATGCCTGGGACCAA | 9866 |
rs7935453 | snp | C/G | 0.426491 | 0.177062 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8625216 | AGCCCATGATGCTCA[C/G]CGAGGTGGAGTGCTG | 9866 |
rs7939673 | snp | A/G | 0.493703 | 0.0557558 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649200 | AAACATTAGCTGGGC[A/G]CGGTGGCGCATGCCT | 9866 |
rs7941510 | snp | A/C | 0.460589 | 0.13473 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655516 | GGCCAGGCACGGTGG[A/C]TCATGCCTGTAATCC | 9866 |
rs7941744 | snp | A/C | 0.279726 | 0.248226 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625624 | CCTAAGCAAAGGGTC[A/C]GGCTGTGGGACTGCC | 9866 |
rs7942340 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653464 | gaagatgagagatca[C/T]gcagagaaagttctc | 9866 |
rs7942680 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626491 | GCAAGTCAGATCCTA[G/T]GAAGGAGGCATCAGT | 9866 |
rs7943945 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8620335 | TGTCAGGCATAGGAC[A/G]AAGAAATGTATCCAG | 9866 |
rs7946508 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619954 | CTCAGAATTTTGTGA[A/C]TCTAGAAAAACAGGG | 9866 |
rs7947230 | snp | G/T | 0.369294 | 0.219702 | missense, nc-transcript-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8625123 | CACCAGCTGTCAGGT[G/T]GCTCACACTCTGGAT | 9866 |
rs7950166 | snp | C/T | 0.499437 | 0.0167637 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620671 | GAGAAACTGAGTCTC[C/T]GGCTTTGCCGTGTAA | 9866 |
rs7950528 | snp | C/T | 0.485799 | 0.0830599 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655638 | AAATACAAAAATTAG[C/T]CAGGCGTGGTGGTGG | 9866 |
rs7950801 | snp | C/T | 0.110872 | 0.20771 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648625 | GCTTTGCTGCACAGC[C/T]CTCAGCCTTCAGAGG | 9866 |
rs7951084 | snp | C/T | 0.298265 | 0.245297 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683933 | GTGATCTACCCCCCC[C/T]CGTCCTCCTAAAATG | 9866 |
rs9633894 | snp | C/T | 0.255503 | 0.249939 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631812 | ATATGAGTTTATGAT[C/T]TCCTACAGAATATAA | 9866 |
rs10128597 | snp | A/G | 0.457037 | 0.140127 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673283 | CACACATATTTTCAT[A/G]AGTTCTGTCCACTAA | 9866 |
rs10160373 | snp | C/T | 0.376791 | 0.215463 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623963 | GTTAGGTATCTTACC[C/T]GGGATCACAGGGAGA | 9866 |
rs10533257 | snp | A/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8623019 | ACTATAGTCATTCAT[A/T]CATAGTGGTGACAAG | 9866 |
rs10591325 | in-del | -/GCCTC | 0.277867 | 0.248442 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646942 | GGCAGAATGCATACT[-/GCCTC]AGTAGTTTCTGAGGG | 9866 |
rs10604996 | in-del | -/AA | 0.29175 | 0.246489 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647446 | ATCGCTAACTGAAAG[-/AA]TGGCAAGAACTGAAC | 9866 |
rs10734634 | snp | A/T | 0.29046 | 0.246704 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614609 | GCAAAGGCTCAATTC[A/T]GGCGTTCAGAAAGGA | 9866 |
rs10734635 | snp | A/C | 0.0185938 | 0.0946107 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614796 | GCCATGGAACAGAGC[A/C]TATGGAAGGTATGGT | 9866 |
rs10743083 | snp | A/G | 0.329317 | 0.237084 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614803 | AACAGAGCATATGGA[A/G]GGTATGGTTGCCACT | 9866 |
rs10743084 | snp | A/G | 0.37138 | 0.218556 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635774 | CCAACTTGCAGCCAC[A/G]CAAAAGGGCAGCACC | 9866 |
rs10743085 | snp | A/G | 0.266819 | 0.249434 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637587 | AAACTCTCCTCAAGT[A/G]TCACGGAGACTGACT | 9866 |
rs10769930 | snp | A/T | 0.286016 | 0.247392 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614350 | TCTCTCAAAAAATAA[A/T]AAATAAATAAATAAA | 9866 |
rs10769931 | snp | C/T | 0.496968 | 0.0388195 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614558 | AGCAGTACTGAGGGA[C/T]GGAGAAGAAGCCCAG | 9866 |
rs10769932 | snp | C/G | 0.498813 | 0.0243321 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614792 | GACTGCCATGGAACA[C/G]AGCATATGGAAGGTA | 9866 |
rs10769933 | snp | C/G | 0.330249 | 0.23677 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616379 | CCTTGAACTTCATCT[C/G]TTAGCAAAAATAAAG | 9866 |
rs10769934 | snp | G/T | 0.267091 | 0.249415 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627950 | CCTCCCACCTCAGCC[G/T]CCAGAGTAGCTGGGA | 9866 |
rs10769935 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629348 | CATGTATGTTTAGTG[C/T]GGTTTTGGCGCTCAT | 9866 |
rs10769936 | snp | C/T | 0.483923 | 0.0882034 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632981 | GGAGGACAGAAAAAG[C/T]AAAGAGGATCTCAGA | 9866 |
rs10769937 | snp | C/T | 0.267091 | 0.249415 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643322 | CCTCTTATCAAGGCT[C/T]CTGGAACCTACATTC | 9866 |
rs10769938 | snp | A/G | 0.472429 | 0.114129 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650000 | TTCCTCCACCAGTTT[A/G]GAGTGTAACCTATTC | 9866 |
rs10769939 | snp | C/T | 0.496314 | 0.0427728 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662092 | AAGCCACTCCACTGA[C/T]AGGGCTCCAGGCTCC | 9866 |
rs10769940 | snp | A/G | 0.482757 | 0.0912364 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680922 | CCAACAGATTAAAGT[A/G]CAACAGAAAGAACAA | 9866 |
rs10840096 | snp | C/T | 0.279726 | 0.248226 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622442 | TCCCCAGCTGAATTG[C/T]TACTCCAGATCCTCT | 9866 |
rs10840097 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629357 | TTAGTGTGGTTTTGG[C/T]GCTCATTTAATCTAC | 9866 |
rs10840098 | snp | C/G | 0.253824 | 0.249971 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645429 | GCACACTGCTCATGT[C/G]CAGGGTAATGTCTGA | 9866 |
rs10840099 | snp | C/T | 0.499035 | 0.0219437 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646133 | AAATGAATAAATGTC[C/T]ACATCTCTTGGGCAT | 9866 |
rs10840100 | snp | A/G | 0.498908 | 0.0233371 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647890 | CTTCACAGGCACTAC[A/G]TCTGACGGCCTGGTG | 9866 |
rs10840101 | snp | C/T | 0.342445 | 0.23228 | synonymous-codon, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8649822 | TGTGCAAGAGCTGCA[C/T]AGCCAGCGATTGCAG | 9866 |
rs10840102 | snp | C/T | 0.459914 | 0.13578 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654691 | gtaggttcttggaaa[C/T]ggcaactttaagtat | 9866 |
rs10840103 | snp | C/T | 0.357451 | 0.225731 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8660918 | TAAGGCTACAACATA[C/T]AGAGAAATGACAGGA | 9866 |
rs10840104 | snp | C/G | 0.46014 | 0.13543 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668710 | CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGATTA | 9866 |
rs10840105 | snp | A/G | 0.318415 | 0.240457 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678115 | AGTAACATAAAATGA[A/G]TCACAAAAATGTTCA | 9866 |
rs10840106 | snp | C/T | 0.359998 | 0.2245 | intron-variant | TRIM66 | GRCh38.p7 | 11:8680289 | GTCATAAGGAGCTAC[C/T]GAACTTTTTGATCAA | 9866 |
rs10840107 | snp | C/T | 0.431473 | 0.171952 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680595 | TGCCACTCACCAAGA[C/T]AGAGAATAAAGGAGA | 9866 |
rs10840108 | snp | C/T | 0.443195 | 0.158668 | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682394 | CAGACCACTAAGAAC[C/T]GTGGAGGTGCGCGGG | 9866 |
rs10840109 | snp | A/G | 0.204803 | 0.245881 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682492 | TTCCCTGACCAAGGC[A/G]CCAGAAAAGGGCCTG | 9866 |
rs10840110 | snp | C/T | 0.204496 | 0.245824 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682544 | GTGCAGTACAGCACA[C/T]CTAGCCCCGATTCTT | 9866 |
rs11042013 | snp | C/G | | | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614565 | CTGAGGGATGGAGAA[C/G]AAGCCCAGGAAGGGG | 9866 |
rs11042014 | snp | G/T | 0.106278 | 0.204558 | intron-variant | TRIM66 | GRCh38.p7 | 11:8620192 | ATGAACTAAAGATGT[G/T]GACCCTGATAACTCC | 9866 |
rs11042015 | snp | G/T | 0.0261823 | 0.111381 | missense, nc-transcript-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8624811 | ACCCAGTTTCTGGCT[G/T]CATGTCAGAAACTGG | 9866 |
rs11042016 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625577 | ACACAGACACACACA[C/T]ACACAGCCATATCCC | 9866 |
rs11042017 | snp | C/G | 0.498945 | 0.022939 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628144 | TCCTGAATGGTAAAT[C/G]TATTTTTTTTTCTTT | 9866 |
rs11042018 | snp | A/C | 0.499673 | 0.0127754 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628160 | TATTTTTTTTTCTTT[A/C]CATTTGTTTTTCTTG | 9866 |
rs11042019 | snp | C/T | 0.383632 | 0.211288 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631045 | CTAATGATTGCCACA[C/T]GGTATTGTCAAAATT | 9866 |
rs11042020 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636862 | CCAAAGCATAATTTA[A/G]AAGGCCTTACAGCCC | 9866 |
rs11042021 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8638706 | CTGTCCACTGGGGGG[A/G]CACTGAGAGGGGTTT | 9866 |
rs11042022 | snp | C/T | 0.178195 | 0.239672 | missense, intron-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640543 | AGGGGAGGTGGGGGA[C/T]GGGGGAGGGGTGGTG | 9866 |
rs11042023 | snp | C/T | 0.482378 | 0.0921983 | missense, intron-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640969 | GAGACTGGGGAGCAG[C/T]GGGAGCAGCACACAG | 9866 |
rs11042024 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643732 | CTCCATTCATTCTAC[C/T]ATCACCTCAATTTAA | 9866 |
rs11042025 | snp | A/C | 0.489024 | 0.0732638 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653928 | AGGTGGAGAAGGATG[A/C]TCTCCACAGGTGACA | 9866 |
rs11042026 | snp | G/T | 0.264358 | 0.249587 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8659338 | GGAGGTCAGGGTAGT[G/T]GAGCATTAATGGGAC | 9866 |
rs11042027 | snp | A/C | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663904 | GTATAAGCTCACTCA[A/C]GTAGAATCTAAAAAA | 9866 |
rs11042028 | snp | A/G | 0.251296 | 0.249997 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664521 | TTTTTCATCTATAAA[A/G]TGGGAATACTAATAC | 9866 |
rs11042029 | snp | A/C | 0.49645 | 0.0419827 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666578 | tatatgtcctcattt[A/C]atcttcacaacagtc | 9866 |
rs11042030 | snp | C/T | 0.460589 | 0.13473 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669171 | ATTTGGTCCAAAGCA[C/T]AGACTGCCTTATGTT | 9866 |
rs11042031 | snp | C/T | 0.000527844 | 0.0162371 | missense, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672022 | ATGTCCACAGCCATG[C/T]CTGTGCCCAGGACTG | 9866 |
rs11042032 | snp | A/T | 0.34526 | 0.23114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675325 | caacaaatactgtca[A/T]ttcacttttgagaaa | 9866 |
rs11042033 | snp | C/T | 0.361894 | 0.223562 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675507 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA | 9866 |
rs11042034 | snp | C/T | 0.447938 | 0.152711 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675680 | agccatcgcacccgg[C/T]ctgccagttgtcctt | 9866 |
rs11042035 | snp | G/T | 0.167484 | 0.23599 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678737 | GTCCACATCTAAAGA[G/T]GGAGAGCAAGAAAAC | 9866 |
rs11042036 | snp | C/G | 0.304438 | 0.244001 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678780 | ATTCAGGATGTTGCT[C/G]CTATCTGAAGGACTG | 9866 |
rs11042037 | snp | C/G | 0.0850919 | 0.187897 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680682 | AATGTCCAAGGAATA[C/G]TAACCAGTAATTAAG | 9866 |
rs11042038 | snp | C/T | 0.336017 | 0.234736 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681186 | TCGCCCAGGCTGCAG[C/T]GCAGTGGCGCGATCT | 9866 |
rs11268493 | in-del | -/GCAGGGAGAGGTGGGATTGGT | | | splice-donor-variant | TRIM66 | GRCh38.p7 | 11:8649737 | AGAGGTGGGATTGGT[-/GCAGGGAGAGGTGGGATTGGT]ACCTGGAGATCCCTT | 9866 |
rs11279624 | in-del | -/TGGTAGCTGC | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8625356 | GAGTCTGGTAGCTGC[-/TGGTAGCTGC]CAGGAACTCAGGCAA | 9866 |
rs11293374 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672638 | TTTTTTTTTTTTTTT[-/T]GAGACAGGATCTCAC | 9866 |
rs11517718 | snp | A/G/T | 0.644248 | 0.0789195 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8671858 | GGAAGCAGTCCTTAC[A/G/T]GAGCAAATGCTGGCA | 9866 |
rs11538027 | snp | A/C | | | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613268 | GTAAGAGGAGAGAAT[A/C]CAGAGACTTGTTTTT | 9866 |
rs11605978 | snp | C/G | 0.341909 | 0.232492 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641488 | GCCCAATCAGACTCT[C/G]ACAAAAAGAATCAAC | 9866 |
rs11607318 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8669568 | gaatcacttgaaccc[A/G]ggaggcagaggctgc | 9866 |
rs11825777 | snp | A/G | 0.103082 | 0.202275 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631189 | GAAAACAGGCTGGCT[A/G]GTCTTGATTCTGTGC | 9866 |
rs12271470 | snp | A/G | 0.49168 | 0.063958 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669465 | CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 9866 |
rs12273403 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677747 | TTGTATAAGCTGTTC[C/T]CAAAGACTCTAGAAT | 9866 |
rs12285011 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669225 | TATTGCTGCTAATAC[C/T]AACAGTGCTATTTAC | 9866 |
rs12286011 | snp | A/G | 0.382473 | 0.212016 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8611792 | AACCTGGAAGGCGGA[A/G]GTTGCAGTGAGCCGA | 9866 |
rs12295729 | snp | C/G | 0.380529 | 0.213219 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637857 | CACTAGGAGGAATGG[C/G]TGGAGGACAGGCACA | 9866 |
rs12362755 | snp | A/G | 0.0403247 | 0.136148 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619349 | TCCTGGGGATGCAGG[A/G]AAATAGGAGAGAGGG | 9866 |
rs12363135 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | TRIM66 | GRCh38.p7 | 11:8680341 | TTTCGGAATACTAAC[A/G]TGGTGGAGGTGTGAA | 9866 |
rs12364516 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667375 | tcatgaaaatttaaa[A/C]ctttgtgcatcccag | 9866 |
rs12575252 | snp | C/G | 0.499859 | 0.0083854 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672526 | GGCTGAGGAAACAGT[C/G]TTAGAGAGGCTGGGT | 9866 |
rs12787554 | snp | A/G | 0.375 | 0.216506 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647022 | TATTGGCATAATAAC[A/G]TATTATATAATAAAC | 9866 |
rs12799863 | snp | A/T | 0.415405 | 0.187459 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670017 | gttttgtttttattt[A/T]tttttttttttttga | 9866 |
rs12801789 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682947 | GCCGCCTGCGGGGCA[A/G]GGTggccggcgcggg | 9866 |
rs12803166 | snp | G/T | 0.472495 | 0.113999 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624690 | AACAAAGGAAGTTTG[G/T]ATAGCATTTCCCCAG | 9866 |
rs12805082 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670169 | aggcacgcaacacca[C/T]gcccggctaattttt | 9866 |
rs12808222 | snp | A/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8628614 | gaagaccctgtctca[A/T]aaaaaaaaaaaaaaa | 9866 |
rs16938564 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | TRIM66 | GRCh38.p7 | 11:8657999 | ATGGCGCTTACCAAG[C/T]GCCCAGGAACACCCA | 9866 |
rs17552254 | in-del | -/T | 0.424519 | 0.179006 | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682431 | AGGGCTGGCGCATTT[-/T]GGTGAGGAGCTCAGA | 9866 |
rs28476482 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632712 | GTGACCCACTTGCCT[C/T]GGCCTTCCAAAGTGT | 9866 |
rs28523683 | snp | A/T | 0.388964 | 0.20782 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670013 | TCTTGTTTTGTTTTT[A/T]TTTATTTTTTTTTTT | 9866 |
rs34010112 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683710 | GTGTGTGAGACTGAT[C/T]ACTGTCGCCCAGGCT | 9866 |
rs34011608 | in-del | -/A | 0.369754 | 0.219451 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633322 | CTCAAAAAAAAAAAA[-/A]TTATTTTGAATAGGA | 9866 |
rs34023476 | in-del | -/C | | | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615839 | AAATTTGTGGTCTCC[-/C]AATTGCTCCTGAGGA | 9866 |
rs34077047 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8624107 | ATAATGCAGACCCCC[-/C]AGGACTCTTTGCATG | 9866 |
rs34113555 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8641930 | TTCCTGAGGCCTCCC[-/C]AGAAGCCGAGCAGGT | 9866 |
rs34273874 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679773 | CTGCTGGTCACATGC[-/C]AGTATGTGATTAAGG | 9866 |
rs34326624 | in-del | -/A | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8647095 | AACAATAAACATATA[-/A]TATAATGTTTATTAT | 9866 |
rs34350913 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8645913 | GAGAAGACAGAGTCC[-/C]TTGATCCTGTTACTG | 9866 |
rs34361529 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8639716 | ATATAAAACATACCC[-/C]AGCTTAGTAGAAGTA | 9866 |
rs34386713 | in-del | -/CATA | 0.499325 | 0.0183582 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623016 | TACACTATAGTCATT[-/CATA]CATAGTGGTGACAAG | 9866 |
rs34430660 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8670473 | AATGCTGGAACTTTC[-/C]AAGATATATTTATGA | 9866 |
rs34655699 | snp | C/G | 0.308661 | 0.24302 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638570 | GGACGCTCCTCCCCC[C/G]ACCCTATCCTCCTCC | 9866 |
rs34770358 | snp | A/T | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647093 | TAAACAATAAACATA[A/T]AATATAATGTTTATT | 9866 |
rs34814686 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8629253 | TGAACAAGAACACCC[-/C]AGTGACTATTTCATT | 9866 |
rs34867877 | snp | C/G | 0.499809 | 0.00978247 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655654 | CAGGCGTGGTGGTGG[C/G]CACCCTGTAATCCCA | 9866 |
rs34873032 | in-del | -/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8648351 | CACGGGGATTCCCAG[-/G]AGCTCTCACAAGTAA | 9866 |
rs34898278 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665534 | GTCAAGGGCTCTGTC[-/C]TTTTCATCTCTGTAC | 9866 |
rs34999106 | in-del | -/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8621907 | ATGATCCCTGTGATG[-/T]ATTAATATTGAGTGT | 9866 |
rs35023845 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8680046 | TGTTGGTTGTTATCC[-/C]TTGTGGACTGAAGTG | 9866 |
rs35075752 | in-del | -/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8651437 | GAATTTCAACTCAGG[-/T]ATGATTAAAAAAATA | 9866 |
rs35133962 | in-del | -/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8648247 | TCTTGGCCCATTAGG[-/G]CCTTTTCCAGGGAAG | 9866 |
rs35179986 | in-del | -/GCT | | | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681652 | GAGCGAAGACATGCT[-/GCT]ATTAGCGAAGACAGG | 9866 |
rs35204530 | in-del | -/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8671117 | TTCAAATCACTTGGG[-/G]AAATACTGCAGAGAA | 9866 |
rs35317559 | in-del | -/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8670030 | TATTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 9866 |
rs35319120 | snp | C/T | 0.46137 | 0.133501 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648147 | TTTGAGCATGCCAAC[C/T]AAGCGGGAATCTCCA | 9866 |
rs35503738 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8648483 | TGTCTCACAGAATAG[-/G]CTTGAGTACTTCCTG | 9866 |
rs35578541 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639850 | GGGATTCATAAGGTC[C/T]GGCAAGGGAGCTAGG | 9866 |
rs35654858 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8669755 | CCAGGGTCAGAGATT[A/G]TTAAGCAACACTGCA | 9866 |
rs35703499 | in-del | -/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672957 | TTTTTTTTTTTTTTT[-/T]AAGATGGAGTCTTGC | 9866 |
rs35779074 | in-del | -/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8636568 | GGATGGGAGCATGGG[-/G]AAAACACCTGGGTGT | 9866 |
rs35847366 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642472 | GTCTACATTCTGCCT[A/G]AAGACTGAATGCCAG | 9866 |
rs35904890 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649229 | CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAAGC | 9866 |
rs35905151 | in-del | -/G | 0 | 0 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680457 | GCCTGAATGAAGGCA[-/G]GGGCACTAAGGCTTA | 9866 |
rs35981610 | in-del | -/C | 0.320814 | 0.239761 | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682426 | GCTCAGGGCTGGCGC[-/C]ATTTGGTGAGGAGCT | 9866 |
rs36053705 | in-del | -/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8639980 | TCCAGGAAGACAGGG[-/G]CTAAGCCAAGCTACT | 9866 |
rs36060657 | in-del | -/C | | | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660326 | GCGTGTGCCTCATCC[-/C]TAACACTATTCCCTA | 9866 |
rs36092927 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670792 | AAATCAAAATAGATC[A/G]TATCTTTCCTGTACT | 9866 |
rs36101030 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664143 | AGTGTTCTCACCACC[-/A]AAAATGATAACTATG | 9866 |
rs55707895 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8637463 | GTACCTCAAGGGCCT[C/T]TATGCCAAGTCATTT | 9866 |
rs55732506 | in-del | -/GAGAGA/GAGAGAGA | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8628645 | AAAAAAAGAGAGAGA[-/GAGAGA/GAGAGAGA]ATCCAGATCTTTGGT | 9866 |
rs55733010 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657210 | AGGCCACCAAGTGAG[A/G]ACACACTCGTTGCAT | 9866 |
rs55759383 | snp | A/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8647094 | AAACAATAAACATAT[A/T]ATATAATGTTTATTA | 9866 |
rs55780316 | snp | C/T | 0.0788843 | 0.182262 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620782 | AGGCTGGGGTAGTAG[C/T]ATAGGCACAAATCCA | 9866 |
rs55931237 | snp | G/T | 0.0655868 | 0.168795 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681262 | CCTCAGCCTCCCGAG[G/T]AGCTGGGACTACAGG | 9866 |
rs56293232 | in-del | -/ATAT | 0.0441095 | 0.141807 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637322 | ATAATCATTTAATGC[-/ATAT]ATATATATATATATA | 9866 |
rs56321966 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666772 | TATTCTTCATTGCAA[C/T]TAGAATAACTTGGCA | 9866 |
rs57012665 | snp | C/T | 0.326741 | 0.23793 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673179 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 9866 |
rs57188799 | snp | G/T | | | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682390 | CGGGCAGACCACTAA[G/T]AACTGTGGAGGTGCG | 9866 |
rs57836157 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630506 | TTTGAGATTCACTAC[C/T]GAAAATAAACTATTT | 9866 |
rs58353604 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612861 | CAGGCTCTAACTGGT[A/G]CAGGATCATGGTGAG | 9866 |
rs58421279 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664015 | GATGTTGGTGAAAGA[A/T]TACAAAATCCAAGTT | 9866 |
rs58505829 | snp | A/G | 0.101301 | 0.200969 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642083 | TCAGTGCCAGGCACC[A/G]GCACTGCCCCCTGAG | 9866 |
rs58555983 | snp | G/T | 0.0513262 | 0.151752 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660822 | GGATGTTTCAAGCAA[G/T]AAAAGGCATTTCAGG | 9866 |
rs58687341 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8676445 | TCTCAGGGACCCCCC[-/C]ACCCCATAAGGTCTA | 9866 |
rs59189365 | in-del | -/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8632776 | CACATGTTGATTTTT[-/T]AATGGCAAAGTTGTT | 9866 |
rs59752192 | snp | A/G | 0.0678174 | 0.1712 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681179 | CGTTCTGTCGCCCAG[A/G]CTGCAGTGCAGTGGC | 9866 |
rs60267562 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626592 | ATATACCCACTAATT[C/T]TTCCCTCTGCTAATG | 9866 |
rs60432547 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8642868 | AAAAAAAAAAAAAAA[-/A]GGTTTGCTGAATGAT | 9866 |
rs61045588 | snp | C/T | 0.0501905 | 0.150254 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680469 | GGCAGGGCACTAAGG[C/T]TTAAACAGAGGAAGC | 9866 |
rs61730185 | snp | A/G | 0.0209915 | 0.100275 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8645796 | CAGACAGCCCAGTTG[A/G]TGAAATTCTGCACAT | 9866 |
rs61738062 | snp | C/T | 0.0338882 | 0.125681 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8649829 | GAGCTGCACAGCCAG[C/T]GATTGCAGTAGGTGC | 9866 |
rs61741649 | snp | C/T | 0.115817 | 0.210938 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8646535 | TGGTTTTCCACCTTC[C/T]TATGCTGATGCTTCA | 9866 |
rs61742770 | snp | C/G/T | 0.00321626 | 0.0399749 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8646469 | TCCTCTATTAGCCCA[C/G/T]TGGCCTGTTTGTTCA | 9866 |
rs61743935 | snp | A/G | 0.116123 | 0.211133 | missense, intron-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8641102 | CCTGTAAGCCTCCAT[A/G]AGCAGGAGCATCTGC | 9866 |
rs61875910 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644864 | ATTCCCAGATCCAGA[A/G]GCTGCTCGTCACTAT | 9866 |
rs61875912 | snp | C/G | 0.175897 | 0.238765 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8659891 | TGTTTGTCTTTGTTT[C/G]TTTTGAGACAGTGTT | 9866 |
rs61875913 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673914 | GGAGCCAAGCCTTCA[A/C/G]GAAGGAGGAAGGGTG | 9866 |
rs61875926 | snp | C/G | 0.14651 | 0.227574 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683981 | AGCCATCACACCGGC[C/G]CCACGTAGCTTTGTA | 9866 |
rs62622852 | snp | C/T | 0.226779 | 0.248919 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617784 | ATGTACTACGGCTCC[C/T]AAATAAATGCTGTAG | 9866 |
rs66520755 | in-del | -/AAAA/T/TAAAT | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670017 | TCAAAAAAAAAAAAA[-/AAAA/T/TAAAT]AAAAACAAAACAAGA | 9866 |
rs66745246 | in-del | -/TA | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647093 | TAAACAATAAACATA[-/TA]ATATAATGTTTATTA | 9866 |
rs67165472 | snp | A/G | 0.144632 | 0.226711 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643363 | TTTTTTAATTGAGAC[A/G]GGGTCTCACTCTGTT | 9866 |
rs67331570 | in-del | -/TGC | 0.322721 | 0.23919 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681648 | TTAAGAGCGAAGACA[-/TGC]TGCTATTAGCGAAGA | 9866 |
rs67365081 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634022 | TACATCTCAGGCTCC[C/T]AAGCCATGAGCCGCA | 9866 |
rs67401071 | in-del | -/TATATATATATATATATATATATATATATGTGTGTGTGTGTGTG | 0 | 0 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622366 | ATATATATATATATA[lengthTooLong]TGTGTGTGTGTGTGT | 9866 |
rs67701052 | in-del | -/A/GG | 0.5 | 0 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683933 | CATTTTAGGAGGACG[-/A/GG]GGGGGGGTAGATCAC | 9866 |
rs71452476 | in-del | -/ATAC | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623017 | ACACTATAGTCATTC[-/ATAC]ATAGTGGTGACAAGT | 9866 |
rs71452477 | in-del | -/AGAGAG/AGAGAGAG | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628644 | AAAAAAAAGAGAGAG[-/AGAGAG/AGAGAGAG]AATCCAGATCTTTGG | 9866 |
rs71452478 | in-del | -/C | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632200 | CAGTCTCAGCTACTC[-/C]AGGAGGCTGAGGCAG | 9866 |
rs71474997 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615222 | GCGTGAGCCACCGCG[C/G]CCAGCCAAAAAATAA | 9866 |
rs71474998 | snp | A/G | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8640067 | TTTTCTGAGGTGGGA[A/G]GTTGAGCCCAGCATA | 9866 |
rs72205134 | in-del | -/TATA | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8637333 | ATGCATATATATATA[-/TATA]TATATGCATTATATA | 9866 |
rs72232543 | in-del | -/TT | 0.250732 | 0.249999 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681135 | GGGAGAATTTTGGAA[-/TT]TTTTTTTTTTTTTTT | 9866 |
rs72856521 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628950 | TTATCTCTCCAAAGA[A/G]AAGTATGCTTTTTAT | 9866 |
rs72856523 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8631597 | ATGCAGGGCTTAGCT[C/T]GTTCTTTCAGTGAAT | 9866 |
rs72856558 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654893 | TGACGTGGAGTCTTG[C/T]TCTGTCACCCAGGGT | 9866 |
rs72856576 | snp | C/T | 0.0629771 | 0.165899 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673335 | TTGTGATAATAAAGT[C/T]TTAAAAAGTATAGTC | 9866 |
rs72856592 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681100 | TCTTTTGGGGAGCTT[C/G]GCTGTAAGGGCAAGG | 9866 |
rs73408082 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637905 | AGATGTATGACAGGG[G/T]TTGGGGGTGAAGGGG | 9866 |
rs73408102 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654741 | AGTTTTCTTCATCAA[C/T]GTTATAACAAAAGGA | 9866 |
rs74053012 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638361 | TGAAGCAGCACACAC[A/G]GTTCCAAGCACAGAG | 9866 |
rs74053014 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648970 | TGAACTCTGGTTCCT[A/G]TGGATTTGACAGTTG | 9866 |
rs74055103 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679113 | GTCCCATGTGCCTAG[A/C]TGGGAGGGACAGGTC | 9866 |
rs74503680 | snp | C/G | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666341 | CAAAACTCCGCCTCA[C/G]AAAAAAAAAAAAAAA | 9866 |
rs74616416 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628945 | ATCTTTTATCTCTCC[A/G]AAGAAAAGTATGCTT | 9866 |
rs74640813 | snp | A/T | | | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621602 | AAAGAATAAGCTCTT[A/T]GGCTGGGCCAGGGTT | 9866 |
rs74933132 | snp | C/T | 0.000470079 | 0.0153238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618023 | AAGAAAAATATATAT[C/T]TGGAATTAAAATAGC | 9866 |
rs74962084 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637819 | AGAGAAGACAATAGC[A/G]TAAGTGAAACAGGGC | 9866 |
rs75004016 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628634 | AAAAAAAAAAAAAAA[A/G]AAAGAGAGAGAATCC | 9866 |
rs75015732 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679582 | GCTCTAATACCACTG[A/G]TGGTTCCCTTTCATT | 9866 |
rs75033840 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662991 | TTGACCTGGGACCAT[G/T]CTTAATTAGCCAAAA | 9866 |
rs75064825 | snp | G/T | 0.0287284 | 0.116357 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8611878 | CAAAACAAAAAATAA[G/T]AAGAAGAAGAAAAAG | 9866 |
rs75110590 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615148 | TGGCCAGGCTGGTCT[C/T]GAACTGCTGTCCTTA | 9866 |
rs75449379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679388 | TGTTAGGTGAACACA[A/G]AACCCAACGGGTAGT | 9866 |
rs75602286 | snp | C/T | 0.0402882 | 0.136092 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614581 | AAGCCCAGGAAGGGG[C/T]GATCCAGAAGGAGCA | 9866 |
rs75651224 | snp | G/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683615 | AGCGGGACACAGAAG[G/T]CTGGGAAACACTCTG | 9866 |
rs75676708 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667882 | AGAAACATGGGTGTA[A/C]AAATATCTCTTCAAG | 9866 |
rs75701989 | in-del | -/TT | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8676247 | TTCTTTTTTTTTTTT[-/TT]AACCGGCAGATGCTT | 9866 |
rs75712193 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657127 | GGCCAAGGCAACACG[A/G]ACACCAGAGAGGTAG | 9866 |
rs75744729 | snp | C/T | 0.123105 | 0.215401 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667967 | GGATAATTTGATTTT[C/T]AATTTTCTGAGGAAC | 9866 |
rs75780186 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662587 | AGAATTGCCCAGTCA[A/G]TTAGTGCTAGTGTCC | 9866 |
rs75862334 | snp | C/G | | | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621604 | AGAATAAGCTCTTAG[C/G]CTGGGCCAGGGTTTA | 9866 |
rs75877012 | snp | G/T | 0 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614946 | CAATTTTTTTTTTTT[G/T]GAGACGGAGTCTCGT | 9866 |
rs75984823 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683094 | GCTTTCCCAAACGCT[C/T]CAGAAGTTAGGTCTT | 9866 |
rs76006292 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639998 | AAGCCAAGCTACTCC[A/G]GAGTATACTGAGCCT | 9866 |
rs76016496 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629584 | ATTGGCTCTCCTGTC[C/T]TAATTACCTATTGCA | 9866 |
rs76022785 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646855 | AAAAGAGAAAGTATG[A/G]GAATAATTTACTGTA | 9866 |
rs76023987 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653107 | GTAATGCAATAAACT[C/T]AATTACCAACTCTCT | 9866 |
rs76075033 | snp | G/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8659679 | CTCTTGTGTGTGGGT[G/T]TGGGACTGGGAATCT | 9866 |
rs76178622 | snp | C/T | 0.0486741 | 0.148216 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682491 | GTTCCCTGACCAAGG[C/T]GCCAGAAAAGGGCCT | 9866 |
rs76204778 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635455 | CCTGCCCAACCCCAG[A/C]TCCAAGGCAACAAAT | 9866 |
rs76220304 | snp | C/G | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647961 | TGGCAAGGCACTAGC[C/G]TGTGCTACCTGTCCT | 9866 |
rs76295487 | snp | C/G | 0.0256215 | 0.110247 | intron-variant, utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8624305 | ACCTAGAAGTGCTGA[C/G]TCCATCTGCTCAAGT | 9866 |
rs76302958 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643350 | TTCTTTTTTTTTTTT[A/T]TTTAATTGAGACGGG | 9866 |
rs76314648 | snp | C/T | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656973 | CAACTGCAGGACCCA[C/T]GAGCAGGCCTAGAGT | 9866 |
rs76553652 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635322 | GATAAAGAGATAAAA[C/T]GAAATAATCCATGTA | 9866 |
rs76591417 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669855 | GACCATCTCATTTAT[A/T]TCTTTTAAGTTTTAT | 9866 |
rs76600773 | snp | C/T | 0.078151 | 0.181571 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654637 | CTGGTTTTTAGCAGA[C/T]TGAACAATTATAGAG | 9866 |
rs76613594 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672349 | CTTCAAAAGTGTCCC[A/G]TACCTGTGCCTCTCC | 9866 |
rs76683401 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667653 | ATCTCATGTAACCAG[A/C]ATCATACAGTACTTG | 9866 |
rs76685376 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665129 | TTTAAAAAAAAAAAA[A/C]CAGATTTCTGCCCAG | 9866 |
rs76857306 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8663253 | CTAGGCTGTGGCTGT[A/G]TTAATTAAAGATTTG | 9866 |
rs76876925 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628636 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAATCCAG | 9866 |
rs76885764 | snp | C/T | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653391 | ATATAATTCTGCTCT[C/T]GTTCTTAGAACTTTA | 9866 |
rs76955672 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636376 | AAGAACCCATCAGGC[A/G]GTTACAGCAACTCTC | 9866 |
rs76956644 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615386 | AATCTAGAACTCACC[A/G]TATTTCCACTGCATG | 9866 |
rs77007523 | snp | G/T | 0.123798 | 0.215808 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8611881 | AACAAAAAATAATAA[G/T]AAGAAGAAAAAGCAG | 9866 |
rs77052189 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677478 | TCAATATAATTCAGT[G/T]AGTAAAAACAGAACT | 9866 |
rs77062332 | snp | C/T | 0.040671 | 0.13668 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613595 | TTGTGGAGAACTTGT[C/T]TGCAGGCTGTGTGGA | 9866 |
rs77131596 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634488 | CCTTTGAGGAAAGGA[C/T]TGTGTGTATTTTTCG | 9866 |
rs77154912 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8663252 | GCTAGGCTGTGGCTG[G/T]ATTAATTAAAGATTT | 9866 |
rs77186796 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631142 | TTCCCAAGCTCATAC[A/G]GGTCCAAGACTAGGA | 9866 |
rs77215306 | snp | A/G | 0.117537 | 0.212022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626856 | ATTCACTGAACTCTA[A/G]TCACTCATTTTTTCC | 9866 |
rs77232328 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642423 | CATCAGTTTAACACT[C/T]GTTAGGCTGTCAACA | 9866 |
rs77250884 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657559 | CTGATTACCTCTGTA[A/G]CCACAGGTAAGATGC | 9866 |
rs77335324 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644221 | TAATTCCCTCCCCAT[C/T]GCCAACTCCTACTCT | 9866 |
rs77344919 | snp | A/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684614 | CTGACACTGCTCTAC[A/T]CCAGTGAATAATTTA | 9866 |
rs77374023 | snp | A/T | 0.0448719 | 0.142907 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8680060 | CCTTGTGGACTGAAG[A/T]GTTCTGGGAAGAAGC | 9866 |
rs77383738 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682675 | GGAAGCGACTAGCAG[A/G]CGCGCAATCCCGCGA | 9866 |
rs77450953 | snp | C/T | 0.0978373 | 0.19836 | intron-variant | TRIM66 | GRCh38.p7 | 11:8640204 | TGGGCAGAATATGCA[C/T]GCCAAGCCACCCTGA | 9866 |
rs77460164 | snp | G/T | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653392 | TATAATTCTGCTCTT[G/T]TTCTTAGAACTTTAA | 9866 |
rs77477209 | in-del | -/C | 0.0573587 | 0.15934 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645478 | AGAACTACAGACTTT[-/C]CCAACTGAGCTACCT | 9866 |
rs77496841 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652431 | AGGAGGTATTTTTCT[C/G]TTAGTACAGCATATA | 9866 |
rs77663712 | snp | C/G | 0.0333695 | 0.124785 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680666 | TTTACTTTGTCTGTA[C/G]AATGTCCAAGGAATA | 9866 |
rs77774854 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635036 | GACCTCTCCCCAGCA[A/G]AGCCTCGGGCTACTT | 9866 |
rs77813967 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612081 | TTTGTTCTTGAATGT[A/G]TAGGTTCTTTTAAAA | 9866 |
rs77827863 | snp | A/C | 0.0763149 | 0.179815 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629913 | AGTGCTGTGAGAAAG[A/C]CAGCCCAACCCCATT | 9866 |
rs77843566 | snp | G/T | | | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621607 | ATAAGCTCTTAGGCT[G/T]GGCCAGGGTTTAAGG | 9866 |
rs77945468 | snp | A/G | 0.0622301 | 0.165053 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8661092 | AAGCTAGAGGATTTG[A/G]AAGCATAATCACAGT | 9866 |
rs78022088 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671408 | CACTAGTCAGTGTGA[C/T]TCTATTCAAAATCTG | 9866 |
rs78144934 | snp | A/G | 0.013059 | 0.079743 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8625058 | AACACTTGTCAGGCT[A/G]GACACCATTTTGGGG | 9866 |
rs78178190 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | TRIM66 | GRCh38.p7 | 11:8658828 | CTTCAACAGACATTG[A/G]AATCTGTCTCCTACA | 9866 |
rs78181507 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643353 | TTTTTTTTTTTTTTT[A/T]AATTGAGACGGGGTC | 9866 |
rs78276861 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650793 | TAGGTTCACCAGGCA[G/T]ATAAGGGAGGAAAAT | 9866 |
rs78285579 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8661524 | CCACTGATCCCTTTT[C/G]CAGCTGGGCCTGGAG | 9866 |
rs78292995 | snp | C/G | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618603 | ACTGCCCTGCCTTCC[C/G]TGGGGGCTAAGGGGC | 9866 |
rs78323932 | snp | A/G | 0.0441095 | 0.141807 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663805 | CAACCATTAAAAAAA[A/G]GGAAAACCTGTCATT | 9866 |
rs78339306 | snp | A/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644162 | TTCAGTCCACAGGAC[A/T]TCCCAGCTTCCTTTC | 9866 |
rs78482760 | snp | A/G | 0.0143722 | 0.0835437 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647963 | GCAAGGCACTAGCCT[A/G]TGCTACCTGTCCTCA | 9866 |
rs78527725 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675185 | ACAAAAAATCACATT[C/G]TTTAGAATCACCTCG | 9866 |
rs78534649 | snp | C/T | 0.104149 | 0.203046 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633895 | GGCATCAAAATGCTT[C/T]GATAATGGTATAAAT | 9866 |
rs78542709 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626919 | CCACTATCCTCACCC[C/G]CTTCAGATGGACTGC | 9866 |
rs78737968 | snp | A/G | 0.206642 | 0.246211 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652169 | CCTGCCCCATAAACC[A/G]TGCTACTACAGGCCC | 9866 |
rs78748974 | snp | C/T | 0.00478933 | 0.0487004 | missense, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672028 | ACAGCCATGCCTGTG[C/T]CCAGGACTGGGGCTT | 9866 |
rs78793382 | snp | C/T | 0.0402882 | 0.136092 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615998 | GAACAGAGGGTACTT[C/T]GCCAAGCCAACTGAA | 9866 |
rs78832158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643287 | CTTAGCACCTGTCCA[A/T]CCTCCCAGCTGATCC | 9866 |
rs78966200 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680489 | ACAGAGGAAGCACAT[C/T]GGGGAGATACAGAAA | 9866 |
rs79039371 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632079 | ATATGTGAATGCGCC[A/G]GGCATATCACCTGAG | 9866 |
rs79052020 | snp | C/T | 0.103082 | 0.202275 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671019 | GTGGGCCGGGTGCAA[C/T]GGCTCACGCCTGTAA | 9866 |
rs79193118 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623443 | GCGCAAGCAGGGTCT[A/G]AAAAGTTTAACTGCA | 9866 |
rs79215488 | snp | C/T | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656345 | CTTTTTTCTATTTTA[C/T]TCAGTTAATTATTAT | 9866 |
rs79286915 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614947 | AATTTTTTTTTTTTT[G/T]AGACGGAGTCTCGTT | 9866 |
rs79314068 | snp | A/C | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669645 | GAGACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAC | 9866 |
rs79370799 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653665 | AATAAATAAAGTTTA[A/G/T]TTGTTTTAAGCACAA | 9866 |
rs79392768 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627020 | ATTTTTTGCCAGAAA[G/T]CCTTCTTTCATTCTC | 9866 |
rs79413888 | snp | A/G | 0.0349115 | 0.127424 | utr-variant-5-prime, intron-variant | TRIM66 | GRCh38.p7 | 11:8658834 | CAGACATTGAAATCT[A/G]TCTCCTACATACTCA | 9866 |
rs79596408 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639498 | AAAAGAGGTGCACCA[C/T]CCAATATCCTCCTGT | 9866 |
rs79679142 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672337 | GGCGAACAAACCCTT[A/C]AAAAGTGTCCCGTAC | 9866 |
rs79809900 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616035 | AGGAGATTCAAAAAT[C/T]GAAAGGGAAATGACC | 9866 |
rs79826898 | snp | C/T | 0.103794 | 0.20279 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633805 | AGTCATTGTCCAGCT[C/T]TGGGTTTTAATTTCC | 9866 |
rs79953701 | snp | A/T | 0.109814 | 0.206997 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668594 | TATTTTTATTTATTT[A/T]TTTTTTTTTGAGATG | 9866 |
rs80027384 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8671627 | GGCATCAAGAGGATT[C/T]ACTCTGTCTCACAGA | 9866 |
rs80106507 | snp | A/G | 0.0139931 | 0.0824666 | utr-variant-5-prime, upstream-variant-2KB | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682782 | CTCGCGAGACTTGGC[A/G]AAGGCCTTCCTTTTT | 9866 |
rs80143280 | snp | A/G | 0.00147629 | 0.0271287 | synonymous-codon, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8648532 | CAAGGTGAAGTCTCC[A/G]GGACCACCATTCACT | 9866 |
rs80345035 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628632 | AAAAAAAAAAAAAAA[A/G]AAAAAGAGAGAGAAT | 9866 |
rs111226016 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684442 | TATGTAGATTTTCCA[C/T]AGAGTGCTGTTATGT | 9866 |
rs111384522 | snp | A/G | 8.71042e-05 | 0.00659883 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646401 | ACTAGCTTGATATAT[A/G]GATGGTTTCTGAACC | 9866 |
rs111385074 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621574 | CCCAGAGTCAGAATT[A/C]GGGCAGTAGCAGAAA | 9866 |
rs111482508 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655713 | CTTGAAGCTAGGAGG[C/T]GGAACTTGCAGTGAG | 9866 |
rs111643381 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679918 | GACCACCTATGCAGC[A/G]TCTGACAAGTCACCC | 9866 |
rs111644935 | snp | A/C | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647853 | TAGGACATATGCCCA[A/C]ATCTGCTTAACCACA | 9866 |
rs111656735 | in-del | -/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680456 | GGCCTGAATGAAGGC[-/G]AGGGCACTAAGGCTT | 9866 |
rs111667311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670291 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCACC | 9866 |
rs111684267 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681195 | CTGCAGTGCAGTGGC[A/G]CGATCTCGGTTCACT | 9866 |
rs111737778 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643918 | AAGTGTCCAACTTAC[C/T]CTGCTATCCTCTAGT | 9866 |
rs111773066 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647445 | AATCGCTAACTGAAA[A/G]AATGGCAAGAACTGA | 9866 |
rs111892214 | snp | C/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668534 | TGTGACTGCCTGGGC[C/T]TGCTCATAGCATGGA | 9866 |
rs111929730 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625765 | CAAACTCTTATCTGC[C/T]TCAGACCTTCTTTGA | 9866 |
rs111948629 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641619 | GTTGAGCAAGTAGGA[A/C]GGAAGAGAGTGGGGA | 9866 |
rs111950632 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649957 | CACAAGTGGTAAATG[C/T]TCTAAAGACAGGGGT | 9866 |
rs111998125 | snp | A/G | 0.040671 | 0.13668 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617566 | AGGAGGAGTTCAGAT[A/G]TATACATGGCTCCTG | 9866 |
rs112004185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629358 | TAGTGTGGTTTTGGC[A/G]CTCATTTAATCTACC | 9866 |
rs112038102 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681864 | TGCATTGTGTCCAGG[A/T]AAGGGTCACAGGCGT | 9866 |
rs112041226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667006 | TTGTATTTTTAGTAG[A/T]GACAGGGTTTCGCCA | 9866 |
rs112051004 | snp | A/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8651272 | AGTAAATTAGTAAAT[A/T]ACTAATTTACTAATT | 9866 |
rs112062664 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627143 | TGTCTGTTTCCCCTA[C/G/T]TAAAGTGTAAACTCC | 9866 |
rs112064013 | in-del | -/CTGGTAGCTG | 0.427879 | 0.175668 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625345 | CTCTGGCTTCAGAGT[-/CTGGTAGCTG]CTGGTAGCTGCCAGG | 9866 |
rs112082644 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656321 | ATAAAATATTATTTA[A/G]ATATCATGCTTTTTT | 9866 |
rs112096207 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658537 | ACAACAGTGTTGGTG[A/G]TGAAGTGAGTAGCTG | 9866 |
rs112240789 | in-del | -/A | 0.49655 | 0.04139 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669643 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9866 |
rs112261083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619935 | CAGGCACAAAATTCA[A/G]TAACTCAGAATTTTG | 9866 |
rs112262651 | snp | C/G | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628994 | GTTTAATAGTGTTCA[C/G]TTTTTTAAAAAGCTT | 9866 |
rs112285504 | snp | C/G/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8646944 | CAGAATGCATACTGC[C/G/T]TCAGTAGTTTCTGAG | 9866 |
rs112305581 | snp | A/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632312 | GATTTCATCTCAAAA[A/T]ATAAATAAATAAATA | 9866 |
rs112329022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662053 | GAGAGCCAATTAAGG[C/T]GAGGAAACTGTTCGT | 9866 |
rs112369934 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680526 | GATAGGGTGACAGTG[C/T]AGTAGAAGAAGAGAA | 9866 |
rs112396143 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647870 | TCTGCTTAACCACAG[C/T]TCCTCTTCACAGGCA | 9866 |
rs112469751 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617311 | ACAGCAGCCACCTAT[A/G]TCAACATCAGGAAAG | 9866 |
rs112527898 | snp | C/T | 0.00111586 | 0.0235942 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624663 | CAGTGGCCAATCTTT[C/T]GCCCAATGATGAACA | 9866 |
rs112532960 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647446 | ATCGCTAACTGAAAG[A/G]ATGGCAAGAACTGAA | 9866 |
rs112533323 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683719 | ACTGATCACTGTCGC[A/C]CAGGCTGGAGTGCAG | 9866 |
rs112575617 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TRIM66 | GRCh38.p7 | 11:8655092 | CTCGAACTCCTGACC[C/T]CAAGTGATCCACCCA | 9866 |
rs112580255 | snp | C/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650587 | AAGGACACCCAGATG[C/T]GTAAGCCAAGGATCT | 9866 |
rs112589900 | in-del | -/CT | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612354 | ACCCCTGGAATTCCC[-/CT]GTTCCTTATGTGGCC | 9866 |
rs112621274 | snp | C/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645549 | CACTATGGGATTTGG[C/T]AAAAGATGGTGTTTA | 9866 |
rs112633043 | snp | A/G | 0 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647447 | TCGCTAACTGAAAGA[A/G]TGGCAAGAACTGAAC | 9866 |
rs112739153 | snp | C/T | 0.0414363 | 0.137845 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614861 | GTGTATAGTTAGCAA[C/T]TGCTAGAAGTCAGGC | 9866 |
rs112744221 | snp | C/T | 0.5 | 0 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641776 | TGAGTGGTTTAGCAC[C/T]GTCCCTTTGGTGCTG | 9866 |
rs112803619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648971 | GAACTCTGGTTCCTG[C/T]GGATTTGACAGTTGT | 9866 |
rs112809021 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654564 | ACATTGCATTTTAAA[C/T]ACCTGTTCATATGTC | 9866 |
rs112853000 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643603 | CACCTCGGCCTCCCA[A/C]AGTGCTGGAATTACA | 9866 |
rs112988216 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660354 | CTACCTGGGAGTCCC[C/T]TGCACATTTTTCTGA | 9866 |
rs113000573 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614648 | AGTGACTCCATGGAG[A/T]GAGAGAGGGAGCAGA | 9866 |
rs113015428 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8682191 | AAATGATAGCAAAAG[C/G]GCAAAAGAGAAAGGA | 9866 |
rs113103256 | snp | A/C/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682615 | CCGAAACCGTACACC[A/C/G]CCACCAGGACACTCC | 9866 |
rs113119137 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674140 | TTCTCAAACTTTTTG[A/G]TCTTGGGAATCCCTT | 9866 |
rs113320325 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644438 | TCACCTCCTATTTCA[C/G]AGAGAAAAAAAAGAC | 9866 |
rs113342943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648172 | TCTCCACAGGGAACT[A/G]TCTCAGCCAGACCCA | 9866 |
rs113431845 | snp | C/G/T | 0.0437281 | 0.141251 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627168 | AACTCCATTAGGGTA[C/G/T]GGATTTTTATCTATT | 9866 |
rs113521527 | snp | A/G | 0.000622988 | 0.0176382 | intron-variant, nc-transcript-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684267 | ATCGGCTATTGCCTG[A/G]GTGTGCTAGAGTCCT | 9866 |
rs113534582 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617713 | CATCTGATTACTCTG[A/G]TAATAATAAATACCT | 9866 |
rs113594366 | snp | A/C/T | 0 | 0 | splice-donor-variant, upstream-variant-2KB | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683267 | CCACGGCCGCATAGG[A/C/T]AAGTGCCGGCTTCCC | 9866 |
rs113603104 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634453 | GGATTATAGGCGTGA[C/G]CCACCACACCCGGCC | 9866 |
rs113654653 | snp | A/C/G | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614489 | GTTAAAAGACAAGGA[A/C/G]AGGAGAGAGAGGGCT | 9866 |
rs113734362 | snp | A/G | | | missense, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684026 | CACCGGAAGCACCCC[A/G]GCGGCCGCGGTAATG | 9866 |
rs113782653 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614431 | CATCAGTGTGTGATA[A/G]GCTCTGGGTTCATGC | 9866 |
rs113810655 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643585 | CTGACCTCGTGATCT[A/G]CCCACCTCGGCCTCC | 9866 |
rs113828916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665033 | CTCCATCTGGTTGGA[A/G]GCATTGAAGCTAGGA | 9866 |
rs113938923 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643589 | CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 9866 |
rs113960211 | snp | A/G | 0.0494327 | 0.149241 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655178 | GACTGCATTTTTCGG[A/G]AGTTTGTGTGTTCCA | 9866 |
rs114009276 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666744 | AATATACTGACACCA[A/T]AGCTTTTGTTTTTAT | 9866 |
rs114016419 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624182 | CCATGGCCACAGTGA[A/G]GGAAGCAGAACAGGT | 9866 |
rs114036110 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657321 | CTTGAAGCTGGGGTC[C/T]GAGCTCTGATCCCAA | 9866 |
rs114142211 | snp | G/T | 0.0185938 | 0.0946107 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8659269 | GGCAGCCCAAAAAGT[G/T]TCTGGAGAGTGACTG | 9866 |
rs114180333 | snp | A/G | 0.029116 | 0.117091 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636183 | CCCAGAAGCAACTCA[A/G]CTCAAATGGACAGCT | 9866 |
rs114185559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631980 | ACAGATTTGGGAGTT[G/T]TGTCTAGGAAACACA | 9866 |
rs114213339 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8622255 | GGGACCCTGTGATCA[C/T]GTAAATTAATACTTA | 9866 |
rs114328093 | snp | C/T | 0.0287284 | 0.116357 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681884 | GTCACAGGCGTGTTA[C/T]GTAGATTCTGGAGAA | 9866 |
rs114520191 | snp | A/C/G | 0.0205511 | 0.0992634 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668364 | CTTAAAACATCAGAA[A/C/G]TTTATTACTTTCAAT | 9866 |
rs114668696 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635288 | GAATAAGAAAGTGGC[C/T]TCCTCATAGTATTGC | 9866 |
rs114733189 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673664 | ATAGTTTAGTTTAGA[A/G]AAACATCACATACAT | 9866 |
rs114812342 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615745 | CCAGCAAGCTGATCC[A/G]TGAGCCCAGGAGGCC | 9866 |
rs114815403 | snp | A/G | 0.000975927 | 0.0220683 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672321 | CTGCTGTTTGTCTGA[A/G]GGCGAACAAACCCTT | 9866 |
rs114839797 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657085 | GAAGTGGGGCCCACA[A/C]ATGTCTGTTTCAGAC | 9866 |
rs114860161 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650041 | TCTGGGAGTAACATG[C/T]CGGGGCTTGTGGAAG | 9866 |
rs114901518 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647695 | CTTGTTCTCAAGCAC[C/T]GACTTCTGGCTAGTT | 9866 |
rs114905226 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676991 | TAAAACATTGCCTTG[C/T]CACAAACCACCTCCT | 9866 |
rs114992819 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629270 | GTGACTATTTCATTC[C/T]GTTTTGCAATATATG | 9866 |
rs115041135 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650713 | CCTTCCTGGAACTCA[A/G]TCTAGGAGTGGCTAG | 9866 |
rs115044968 | snp | C/T | 0.0127159 | 0.0787162 | missense, nc-transcript-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8624990 | GTGCTATGCACAAGG[C/T]TGGGCACAGTCTGTA | 9866 |
rs115048647 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8647449 | GCTAACTGAAAGAAT[A/G]GCAAGAACTGAACAA | 9866 |
rs115050548 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636815 | GAAGTCCTTCACTTA[C/T]TCCTCACATCCCCCA | 9866 |
rs115058026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684489 | TCGGCCCTGCCTCTG[A/T]CATTGTCGGTGGTTT | 9866 |
rs115128957 | snp | A/G | 0.0137454 | 0.0817542 | intron-variant | TRIM66 | GRCh38.p7 | 11:8620036 | AGGTGAGAGAACAGC[A/G]TGGCCTTCCTTACCA | 9866 |
rs115132692 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676291 | TATAAGGTTTTGTTC[C/T]AGTTTGGTGCCCAAA | 9866 |
rs115153237 | snp | C/T | 0.0337553 | 0.125452 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616819 | CTCCAACAAAAAGGG[C/T]TGCCAGAAAAGTGTT | 9866 |
rs115244760 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630531 | CTATTTTCTAGTTCA[A/G]AGAGGAAGAGTCAAA | 9866 |
rs115248232 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658917 | TGCCATAGTGACCAA[C/T]TGTCCGTCACAAGCA | 9866 |
rs115251245 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629061 | GGTTGAAGAGAAGCA[A/T]GGTGGAAAGAATATT | 9866 |
rs115339741 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639943 | TCAGAAGGTACCATC[A/G]GTGGGCAGGGTCCCT | 9866 |
rs115399088 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633990 | ATGCCTACCGCTTCT[C/G]TATCATTTACTGGAA | 9866 |
rs115412070 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633378 | ACTTTACACACTATT[C/T]TGTCTTATTAAACAG | 9866 |
rs115418390 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638410 | GCTCTCTTTCCCTTC[C/G]TCCTTCCACTCTGCA | 9866 |
rs115468571 | snp | A/G | 0.00286255 | 0.0377237 | missense, utr-variant-3-prime, intron-variant | TRIM66 | GRCh38.p7 | 11:8621751 | ACAGGCATCTCTCCT[A/G]AGGAGGCAGCACAGA | 9866 |
rs115598617 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619223 | TGCTAAGGCCTGAGT[G/T]TGGGAGAGAGCTTTT | 9866 |
rs115639040 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642610 | ACTGTTGCTGAGATA[A/C]CCCTGCTTGTGCCCA | 9866 |
rs115689547 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623917 | AGGTGCGATTGGCCC[A/C]ATTTAGAGAGAAAGA | 9866 |
rs115695971 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650450 | GAGGAGGAGGGGAAG[A/G]AGCAGAAGGAAAAGG | 9866 |
rs115716718 | snp | A/C/G | 0.00309971 | 0.0392488 | intron-variant, missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8624530 | GTAAGTCAGTGAAGC[A/C/G]AGTGGAATCCTCACT | 9866 |
rs115811045 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612045 | GACGCAATTCTTGGT[A/G]AAGAAAAGTGCTGTT | 9866 |
rs115814838 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637878 | GACAGGCACAGCACT[A/G]AGGCTCCAGCTAGAT | 9866 |
rs115817873 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668199 | TTTTTCTTGGGCTTA[C/T]TGGTTATTTGTACTT | 9866 |
rs115827795 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639447 | GGGGTACAAACTGCA[C/T]CTCTTCAACTGTTTC | 9866 |
rs115831081 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669027 | TTCAAAGGAAACAAA[C/T]AGACTTCACCTCTTG | 9866 |
rs115955769 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634491 | TTGAGGAAAGGATTG[C/T]GTGTATTTTTCGGCA | 9866 |
rs115962032 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632991 | AAAAGTAAAGAGGAT[A/C]TCAGAATCTGAGGTA | 9866 |
rs116010578 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627545 | CAGTAAACCCCAGTT[A/G]TTTCTACTGCTGCTT | 9866 |
rs116014302 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641886 | TGTCCATGTGATGTG[C/T]GTCTTCACCTTCTGT | 9866 |
rs116112207 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669547 | ATTTGGGAGGTTGAC[A/G]CAGGAGAATCACTTG | 9866 |
rs116124055 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628341 | ATCTTGGTTGGGCAT[A/G]GTGGCTCACACCTGT | 9866 |
rs116161531 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615675 | AGCATGCAGGCTCTC[C/T]ACGATGAGAAGGGAG | 9866 |
rs116201274 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628713 | ATACCTCTCTGGGCT[G/T]ACTCCCCTTCACTAT | 9866 |
rs116217292 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652041 | AACTACACTTGATGC[C/T]ATAGCCTGCATTTAG | 9866 |
rs116280420 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670301 | ATAGGCGTGAGCCAC[C/T]GCACCAGGCCTGATA | 9866 |
rs116286752 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647612 | GGGGTGATAAAGCAC[A/G]GATTGCCCCTGGTTT | 9866 |
rs116291856 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650564 | CACACAAGTCCTGTG[C/T]TGAAGCTAAGGACAC | 9866 |
rs116326083 | snp | A/C | 0.0119091 | 0.0762411 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612971 | TGACTTAGATGGGGT[A/C]TCTTAGCAAACAGGC | 9866 |
rs116358005 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682440 | CGCATTTGGTGAGGA[C/G]CTCAGACAACGAGGC | 9866 |
rs116380759 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657444 | GCCAATTCCCCACCA[C/T]ACAGATGATGACATG | 9866 |
rs116407739 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627974 | GCTGGGACTACAGGC[A/G]CATAACATCACATTG | 9866 |
rs116443870 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680505 | GGGGAGATACAGAAA[C/G]AAAAGGATAGGGTGA | 9866 |
rs116596625 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648796 | ACTACCTGCCAGAGG[C/T]TGAGGAAGGCGCTTG | 9866 |
rs116683715 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676711 | ACCCCATTTCTGCCC[A/C]CTTCTTATGGCTGCT | 9866 |
rs116756366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678800 | CTGAAGGACTGATGT[C/T]GAATTCAGGAACCCA | 9866 |
rs116772812 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626836 | CATTCAATAACCCTC[A/T]CCTCATTCACTGAAC | 9866 |
rs116891394 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634375 | GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTCGA | 9866 |
rs116917741 | snp | A/T | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673499 | TGTATTCTTGCCACT[A/T]GAAGTCTAAACAACA | 9866 |
rs117103636 | snp | C/T | 0.0244538 | 0.107838 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613210 | CCACAGACATTTCCC[C/T]CATCTAGGTTTCAAG | 9866 |
rs117184436 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673829 | ACAAAATACAAATCA[C/T]TTAATTCAAATCTGG | 9866 |
rs117203412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636915 | TCCCCAGTGCATCTC[A/G]TGATCCTATCAAGCC | 9866 |
rs117355572 | snp | A/T | 0.0479149 | 0.147179 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613649 | GGAGACTCCAGGGAG[A/T]GGGAGCAGTGGAGTA | 9866 |
rs117482668 | snp | C/G | 0.0327778 | 0.123752 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623685 | CCCAACTAGCCCTCA[C/G]CTTCCACAGAAGAAC | 9866 |
rs117488032 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668565 | GATTGGATTCCAAGA[A/T]GGCATATTCCTTTTA | 9866 |
rs117594333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8661272 | CTGGCTGGGGCTGGA[A/G]ATGGATGCACGATCC | 9866 |
rs117605558 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673973 | GGGTCCAGAAAGATG[C/T]CACTACATAAAGCTA | 9866 |
rs117631225 | snp | C/T | 0.0333695 | 0.124785 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681028 | GTCACAGGCTGTGAG[C/T]TAGACCGCAGTGAAC | 9866 |
rs117635690 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669367 | ACTCCTTTAGGGCCA[A/G]GTGCAGTGGCTCACG | 9866 |
rs117764643 | snp | A/G/T | 0.00389298 | 0.043977 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618974 | CGGAGTCAGGCTGAT[A/G/T]GGGGAGGAGAGCAGT | 9866 |
rs117879704 | snp | C/T | 0.0498192 | 0.149759 | missense | TRIM66 | GRCh38.p7 | 11:8619490 | GCTTCCTCCGGATGA[C/T]TGACAGGTCCATGGG | 9866 |
rs117989651 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667451 | ATATTTGCAAATCAT[A/G]TATCTAATAAGAGAT | 9866 |
rs118054187 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639942 | CTCAGAAGGTACCAT[C/T]GGTGGGCAGGGTCCC | 9866 |
rs118065095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652179 | AAACCATGCTACTAC[A/G]GGCCCAACGCTGCTT | 9866 |
rs118143986 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653781 | TTTAATACTCCCTCA[C/T]CCCACCAAAAAAAAA | 9866 |
rs118169339 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678779 | CATTCAGGATGTTGC[C/T]GCTATCTGAAGGACT | 9866 |
rs137934829 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672938 | ACCTGGCCCATACTC[-/T]TTTTTTTTTTTTTTT | 9866 |
rs137937050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626650 | CTCCCTAGACAACAG[C/T]AGTAGCCTCTTCAAT | 9866 |
rs137940346 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615867 | GGAAGGATCAGGTCT[A/G]AGCCTGTCACAACAC | 9866 |
rs137982443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8661696 | GGTTTTCAGCAGGAT[A/C]CTAGCCCTTCCTGGA | 9866 |
rs137992067 | snp | A/G | 0.000719856 | 0.0189581 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619555 | GGGGAGGAGACATGA[A/G]GAGAAGGAGGCAAAG | 9866 |
rs138002387 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631065 | TTGTCAAAATTCAGA[A/T]AAAACATTGCTCTTT | 9866 |
rs138159937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683408 | TTTTTTCTGACGATC[C/T]TCTAGTATTCCAGTT | 9866 |
rs138176572 | in-del | -/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8668264 | CATTTTAAAATCAGG[-/T]GTTTTTTTTTTTATT | 9866 |
rs138292109 | snp | A/G | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672701 | TCACAGCTCACTGCA[A/G]CCTTGACCTCCCTAG | 9866 |
rs138326262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647004 | GACTAATAATGTTTA[C/T]ATTATTGGCATAATA | 9866 |
rs138327362 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636203 | AATGGACAGCTTTAA[C/T]GCATGATTTCATCTC | 9866 |
rs138383360 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649944 | TTGTGTCTGCCTCCA[C/G]AAGTGGTAAATGCTC | 9866 |
rs138391848 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642045 | TTCTTCACAATAATG[C/T]GAGAATGGACTAATA | 9866 |
rs138444298 | snp | A/G | 0.00919609 | 0.0671824 | missense | TRIM66 | GRCh38.p7 | 11:8620481 | GGCCAGGAGATGCCC[A/G]CATTCCAGGCTGGTT | 9866 |
rs138603159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655426 | ATTAAAATGAGGGAA[C/T]AGGAATGCAGGGGAG | 9866 |
rs138648207 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650229 | AATACAAAAATTAGC[C/T]GGGAGTGGTGGCACA | 9866 |
rs138658090 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679950 | ATTCTTCTGTGCTTC[A/C]GTTTTCACACACGTA | 9866 |
rs138683200 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667465 | TATATCTAATAAGAG[A/G]TTGGTATCCAGAATG | 9866 |
rs138702784 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660713 | GTTTAATTCTGATTA[C/T]GGGGATTTTGCTTGT | 9866 |
rs138716778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670838 | ACTCTGAGAGGCAAG[A/G]TAGCTTGCCCATGGG | 9866 |
rs138815716 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645968 | GTCTGGTGGCTTGTG[C/T]GTGTCACTGATGGAA | 9866 |
rs138874789 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676904 | GGGTCTAATGTCTCC[A/G]AATCTTAGTTTTCCA | 9866 |
rs138905485 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632640 | TTTTTGTATTTTTAC[G/T]AGAGATGGGGTTTCA | 9866 |
rs138978774 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679527 | GCACCCAGAACCCTA[A/C]CTCAACCCCTTGCAG | 9866 |
rs139071920 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682904 | TCATCCACTCCCTAC[C/G]ATGGTCGGGGCTTCC | 9866 |
rs139100548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648659 | CTGCAGAAATACAGA[A/G]CTCGGGGGAAGTGTT | 9866 |
rs139230023 | snp | A/C/G/T | 0.000297371 | 0.0121903 | intron-variant, nc-transcript-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684283 | GTGTGCTAGAGTCCT[A/C/G/T]GAAGAGTAACTGCTG | 9866 |
rs139270819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677537 | TAATCCCAGTGCTTT[A/G]GGAGGGCGAGGTAGG | 9866 |
rs139285033 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8663090 | TACCCAGCCATCCCA[A/C]TGCATGGCTAGGCCA | 9866 |
rs139529507 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684436 | TAGGAGTATGTAGAT[A/T]TTCCATAGAGTGCTG | 9866 |
rs139548275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629349 | ATGTATGTTTAGTGT[A/G]GTTTTGGCGCTCATT | 9866 |
rs139590500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675058 | TCTTGCTCTTTGAAC[C/T]AGTCTTTTCCCCAGG | 9866 |
rs139617087 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633066 | GAAAGCCTGATGAGT[G/T]GAACCCTCAAACCCC | 9866 |
rs139641437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678075 | TGGTGAATAAATTGG[C/T]ACGATCCTTTTGGAA | 9866 |
rs139705308 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680477 | ACTAAGGCTTAAACA[C/G]AGGAAGCACATTGGG | 9866 |
rs139717886 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638507 | GTTGCTGACTCACTA[A/C]GGCAGAAGGCATGAA | 9866 |
rs139729123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624008 | CAAATTCCATCTATC[A/G]GACTCCAAAGTCAGA | 9866 |
rs139785167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642536 | GGCCATGAATTATCT[A/G]CTTACATCTCAACTC | 9866 |
rs139841028 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652186 | GCTACTACAGGCCCA[A/C]CGCTGCTTTGGTTCT | 9866 |
rs140011675 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8652882 | TTATAGTCAGACAAA[C/T]GTAAGTCCAAAATAC | 9866 |
rs140046218 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669597 | GCAGTGAGCCGAGAT[A/C]GCACCACTGCACTCC | 9866 |
rs140053246 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673451 | GTCTCAGGTTAATGA[G/T]CTGAGAGAGGGGCAG | 9866 |
rs140133492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639865 | CGGCAAGGGAGCTAG[C/G]GAGATGACAAGATAA | 9866 |
rs140137014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656918 | TGATATCCCTGTACC[C/T]GGGGATTGGCACTGA | 9866 |
rs140152299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626309 | GCATATCTATCTAAG[C/T]TTCCAAAATCAGTGT | 9866 |
rs140206101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662078 | GTTCGTGAACTAAAA[A/C]GCCACTCCACTGACA | 9866 |
rs140224269 | snp | C/G | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681122 | AGGGCAAGGACATGG[C/G]AGAATTTTGGAATTT | 9866 |
rs140356246 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670172 | CACGCAACACCATGC[C/T]CGGCTAATTTTTGTA | 9866 |
rs140368212 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665685 | AAGTTAAGCCAGGCA[A/C]GGTGGCTCATGCCTG | 9866 |
rs140374311 | snp | A/T | 0.0013235 | 0.0256904 | missense | TRIM66 | GRCh38.p7 | 11:8618844 | CCACTCTCACTAGAC[A/T]CCTCCTCGGAGTCTG | 9866 |
rs140426824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639503 | AGGTGCACCATCCAA[C/T]ATCCTCCTGTGGAAA | 9866 |
rs140434700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654751 | ATCAATGTTATAACA[A/G]AAGGATGTTTACTTA | 9866 |
rs140539822 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643848 | GCCCTCTTCCTCTCC[C/T]AACACTTTCATCTAT | 9866 |
rs140541252 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649659 | GCAAGAAAACAAGAT[C/T]GGAGAGCTATTCTCC | 9866 |
rs140592806 | in-del | -/A | 0.0689305 | 0.172377 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677625 | TTTAAAAACAACAAC[-/A]AAAAAAACAGAACTA | 9866 |
rs140656981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679572 | GTAGGCCCCAGCTCT[A/G]ATACCACTGATGGTT | 9866 |
rs140689733 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681683 | GGGAGGTGAGGGTAA[C/G]TTCATTTATTCACTC | 9866 |
rs140694919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641527 | TGGGAGGGAGTATGC[C/T]AGAAAGTAGCAAAGG | 9866 |
rs140747046 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679046 | CCATGCTGTACTTCA[C/G]AAGAGATGTCACAGA | 9866 |
rs140838730 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658245 | CCAAACTGAACAGCA[A/T]GAGGGAGACCTCAAA | 9866 |
rs140843397 | in-del | -/AT | 0.498945 | 0.022939 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647090 | TAATAAACAATAAAC[-/AT]ATAATATAATGTTTA | 9866 |
rs140857962 | snp | C/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8629966 | TGGCATTTCTGAAAC[C/G]TATATATGCTATGTG | 9866 |
rs140924222 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614000 | GTGGAAGCAGCAAAT[A/G]TGATGATGCCGAAAA | 9866 |
rs140954578 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662501 | ACTAGCTTCAAGAAG[C/G]ATCGGGCTATGGTAG | 9866 |
rs141030464 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | TRIM66 | GRCh38.p7 | 11:8621980 | GTGTCTGTGATGGCA[A/C]TGCCAAAGGAGATTA | 9866 |
rs141069498 | snp | A/G | 0.000366939 | 0.0135401 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8645824 | CATGCTCAAACTGAC[A/G]GTTGAGAACCATGAT | 9866 |
rs141079253 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660163 | TTCAATGGCTCCCCA[C/T]TGTCCACAGAATAGC | 9866 |
rs141142252 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616113 | AGTCCAAAGATTGCC[A/G]GACTAGTAAAGCATT | 9866 |
rs141198519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664206 | AGTCATTCTGCAACG[C/T]ATCTATACTTCAAAA | 9866 |
rs141259325 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648360 | TTCCCAGAGCTCTCA[C/G]AAGTAAGAAATCCAG | 9866 |
rs141273163 | in-del | -/AAAC | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8674037 | TTATTTAGCAGAAAA[-/AAAC]CAGCCATAGCAGCAG | 9866 |
rs141312143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630386 | CTAGCTATAAAGTAC[A/G]TAGAGGGTTATCACT | 9866 |
rs141376902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633878 | CTCAAATTAAGAGAT[C/T]GGGCATCAAAATGCT | 9866 |
rs141394484 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679344 | AGGGTACTCCCTCTA[C/T]AACCAGATCAAGCCA | 9866 |
rs141417246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642290 | CATCAAAGGTCTGCT[C/G]AGTTAAATCAAAGGA | 9866 |
rs141561380 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8672372 | GCCTCTCCTTATTGG[C/T]AGACAAGCTTGACCT | 9866 |
rs141607996 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655484 | CCTACAGCAGCCAGA[A/C]GTTTTTTTTTCCTGG | 9866 |
rs141625845 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655724 | GAGGCGGAACTTGCA[A/G]TGAGCTGAGATTATG | 9866 |
rs141722140 | snp | A/G | 0.000197103 | 0.00992534 | intron-variant | TRIM66 | GRCh38.p7 | 11:8620028 | CAAGGAGAAGGTGAG[A/G]GAACAGCGTGGCCTT | 9866 |
rs141731158 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660816 | TGTGTAGGATGTTTC[A/C]AGCAAGAAAAGGCAT | 9866 |
rs141797116 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615352 | ATTTTTCCTCTAGGG[C/G]TGCATGCTGTCCCAT | 9866 |
rs141841686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679817 | GAAGACCATAATGCT[A/G]TAAGGTCAGAGAGGG | 9866 |
rs141948195 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676709 | TGACCCCATTTCTGC[C/T]CCCTTCTTATGGCTG | 9866 |
rs141962701 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673586 | AAAACTGAGCCATCA[C/T]CATTGTGGCATATGT | 9866 |
rs141982726 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632406 | AAACAGAATCAGATG[A/G]CTGAGGAAGGGACTA | 9866 |
rs142009410 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631497 | AGCAGAGCATAAGGA[A/G]GCTAAGGAGACCATT | 9866 |
rs142067588 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680942 | AGAAAGAACAAGTGA[G/T]ATGAAGAATAGGAAG | 9866 |
rs142087823 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676439 | AAACGGTCTCAGGGA[-/C]CCCCCCACCCCATAA | 9866 |
rs142120648 | in-del | -/A | 0.00319086 | 0.0398152 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644442 | TCCTATTTCACAGAG[-/A]AAAAAAAAGACACCA | 9866 |
rs142124144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632705 | ACCTCCAGTGACCCA[C/T]TTGCCTCGGCCTTCC | 9866 |
rs142127634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639648 | ATATACCTATAAAGC[A/G]GAGATGGTAATGCCT | 9866 |
rs142191510 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635909 | CTGAACCTCATCAAA[C/T]GAGAAGCAGCATTTT | 9866 |
rs142235824 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633263 | GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCGT | 9866 |
rs142361237 | in-del | -/CT | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8639829 | AGCTCTGCCCTCCCC[-/CT]GTCTGGGATTCATAA | 9866 |
rs142386762 | snp | A/C | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654169 | GGCCTCATCACACAT[A/C]CTCTGCTCCCTTGGC | 9866 |
rs142398723 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662903 | GTTTCAGGGATGTTA[G/T]CTCCCTTCAGAGCTT | 9866 |
rs142413611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649507 | ACAATAATTCAACAC[C/T]TTCCTCTCTATACCA | 9866 |
rs142515262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643986 | CATTGATCTCTTGCA[C/T]GGCAACCACCTTGTT | 9866 |
rs142543900 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8651933 | AAGATAGCAGAGTCA[A/G]GGCAACATGGCTGAT | 9866 |
rs142566874 | snp | C/T | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655268 | GAAAAAAAGCCAGTG[C/T]AGGTTTATAAGGAAA | 9866 |
rs142689023 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667700 | TTACCTCATTTAGCA[C/T]AATGTCCTAAAGCTT | 9866 |
rs142698387 | in-del | -/GTGACA | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671234 | ATTCACTGTACCTCT[-/GTGACA]GTGACATGTCCTGTG | 9866 |
rs142718316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674184 | TCATTGAAGACCCCA[A/G]AGAGAGTTCATTTAT | 9866 |
rs142828770 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636447 | TTCAGGTCATCTTCT[A/G]ATGTGTATTCCACAA | 9866 |
rs142886495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669319 | TCAATGGTAATACCT[C/T]GCATCCTCATTGTCC | 9866 |
rs142918756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623829 | AGTGTCAGGTACCAG[A/G]AAAATCCTTACTACT | 9866 |
rs142921344 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679960 | GCTTCAGTTTTCACA[C/G]ACGTAAAATGAGGCT | 9866 |
rs142988643 | snp | C/G/T | 0.00198119 | 0.0314117 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683171 | CTGCCCCTAATTCCT[C/G/T]AGGCCTTACCACCAA | 9866 |
rs143130014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625747 | CAGGGGGTTGAGAAG[G/T]CTCAAACTCTTATCT | 9866 |
rs143179163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652670 | CACAGTGATTCTGCC[A/G]GCCCACCGCAAGGGC | 9866 |
rs143237580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618503 | TCAGCCCAGGTCTGC[C/T]GCTAAATGCTGGGTT | 9866 |
rs143278201 | snp | C/T | 0.00451257 | 0.0472861 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682837 | TGTTTCGTTTCTTGC[C/T]TCCTCTTCCTTGCCG | 9866 |
rs143288154 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622621 | CACCCAGAGCGCATG[C/T]CTCGTGGTGCAGGAG | 9866 |
rs143311121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642106 | CCCCTGAGGCCTCTA[A/G]GTCCCTTGTGCACAA | 9866 |
rs143346984 | in-del | -/T | 0.0376037 | 0.131863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627250 | TGAATTAATGAGCTG[-/T]TTAAAAATTCAAAAC | 9866 |
rs143402749 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626687 | GTATTTTCAAAACAC[A/G]GATCCGATCACATCA | 9866 |
rs143410068 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635360 | ATGAAAAAATTAGAA[C/T]GATACTATACAAAGT | 9866 |
rs143463321 | in-del | -/CA | 0.0166325 | 0.0896639 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618527 | CTGGGTTACCCTGGG[-/CA]GGGACAGGCACCTTT | 9866 |
rs143494265 | in-del | -/ATC | 0.0166325 | 0.0896639 | cds-indel | TRIM66 | GRCh38.p7 | 11:8612742 | CTCCATCCGAATGTT[-/ATC]AGCAGCAGGCACCCA | 9866 |
rs143520802 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664471 | TACCGGGCAGTAGTT[A/G]TTAACCTTAGTCTAT | 9866 |
rs143524373 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665686 | AGTTAAGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 9866 |
rs143588951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669801 | TAACAGTAATCAGCC[C/T]TCTCCTCTGCCCTTA | 9866 |
rs143598657 | in-del | -/TATA | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8637327 | CATTTAATGCATATA[-/TATA]TATATATATATGCAT | 9866 |
rs143636617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683491 | GGTTAGTTGAAGACA[C/T]GGAGTACTGTGGGAA | 9866 |
rs143663424 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628080 | CAAGCCATCTTTCCA[C/T]CTTAGATTCCCAAAG | 9866 |
rs143664755 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613051 | CTGTCCTCCCAGCAG[A/G]AGCTCATAAACATGG | 9866 |
rs143706101 | snp | C/G | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643496 | AGGTGCCCGCCACCA[C/G]GCCCAGCTAATTTTT | 9866 |
rs143822103 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647460 | GAATGGCAAGAACTG[A/T]ACAAAATAATGCATA | 9866 |
rs143841252 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676520 | TCCTGGGAATTCAGG[A/G]AGGTAGCATGGCTTT | 9866 |
rs143849617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662054 | AGAGCCAATTAAGGC[A/G]AGGAAACTGTTCGTG | 9866 |
rs143882371 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615938 | ATGGTGGGAATGTGG[A/G]CTGCACAAAGGAAAG | 9866 |
rs143952266 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680754 | GAAGCCACCCAAGAA[A/G]ACCATGTACTGTGAA | 9866 |
rs144063818 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662212 | GGACACACTGCAGCA[C/T]CTGGAATGAGCAAAG | 9866 |
rs144193401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677849 | TTAGGAATGTAATTG[C/T]CATGTAGAACACTCT | 9866 |
rs144196252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629385 | TACCCATGCTGGACA[C/T]TGAGAATTATATAGA | 9866 |
rs144204042 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633133 | TTTTGCCCAGGCCAG[C/T]GTAGGAAACTGACTT | 9866 |
rs144204188 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633124 | TCAAAGGTATTTTGC[C/T]CAGGCCAGTGTAGGA | 9866 |
rs144317515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627893 | GCAGTGGCACAACCA[C/T]AGCTCACTGCAGCCT | 9866 |
rs144406097 | snp | A/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8675182 | ATAACAAAAAATCAC[A/T]TTCTTTAGAATCACC | 9866 |
rs144427550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677888 | CAGGAAAGAAAGACT[C/T]CTAAAAATTCCTAAT | 9866 |
rs144488623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684476 | TTGAATTTTAGTCTC[A/G]GCCCTGCCTCTGACA | 9866 |
rs144537065 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644219 | CCTAATTCCCTCCCC[A/C]TCGCCAACTCCTACT | 9866 |
rs144558976 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650812 | AGGGAGGAAAATGTT[C/G]TAACAGAGGGAAAGC | 9866 |
rs144650855 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638061 | CTCTGTGTCTCAGCT[A/G]CTCATCTACCTCTGT | 9866 |
rs144736577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8655385 | GGGTAAGTCACCCCC[C/T]TTCACTCAACCTTAC | 9866 |
rs144748284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658389 | CTCTGCACAGCTCGG[A/G]AGACAGCACTCTCAG | 9866 |
rs144768160 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8669167 | TATCATTTGGTCCAA[A/G]GCATAGACTGCCTTA | 9866 |
rs144800362 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8660196 | AATCAAGATCCTTCA[A/C]AATTTGGCCCTAAAT | 9866 |
rs144813266 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612255 | GAAGCAGCACCAGCT[A/G]ATAAGAACTTTCCCC | 9866 |
rs144825557 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616726 | TGCCTCTTGATTTTT[A/C]CCCCTGTCCACCTTA | 9866 |
rs144908149 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676194 | ATTTAATAAAAATTG[G/T]TACCACTTCATCATG | 9866 |
rs144985021 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670201 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCATGT | 9866 |
rs145089151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676858 | GGGCTGGGCAATCTA[C/T]ATGAACGAAGTGCTT | 9866 |
rs145122095 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679456 | TGACCTGAGGGACAG[A/G]ACGTAGCTCCTCTAT | 9866 |
rs145166490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678769 | GAGCTGGATTCATTC[A/C]GGATGTTGCTGCTAT | 9866 |
rs145230911 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680708 | TTAAGTGACCATATG[A/G]GTGTGGAGCTCAGCA | 9866 |
rs145233037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634212 | GCTCTGTTGCCCAAG[C/T]TGGAGTGCAGTGGCG | 9866 |
rs145239621 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617792 | CGGCTCCCAAATAAA[C/T]GCTGTAGATGCAAAT | 9866 |
rs145246518 | snp | A/G | 0.00209278 | 0.0322802 | missense, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8638676 | ACCACATTTGGAGAG[A/G]AGTGCTGGATGGTGC | 9866 |
rs145394332 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8612030 | TGAAAAACACTCCAG[A/G]ACGCAATTCTTGGTA | 9866 |
rs145405067 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615460 | CCATTATGGGAATAA[C/G]TCAAAAGCAGGATCA | 9866 |
rs145410907 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679136 | GACAGGTCCCCTAAT[A/G]CCAAATATCTGGCTG | 9866 |
rs145447381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634969 | AGTGGGATGGAGGAC[A/G]AAACACCTTTACCAG | 9866 |
rs145547189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630045 | ATATTAAAACAAAAG[A/G]TACTTATTTCATGTA | 9866 |
rs145548795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654090 | AGATGCCCAAACATC[A/G]GTCATTGTAACATGG | 9866 |
rs145562424 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8657645 | GTATCCTCTGGCAGG[C/T]TGGACATCCTCACCA | 9866 |
rs145587315 | snp | G/T | 0.00454944 | 0.0474765 | missense, nc-transcript-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8624903 | AGGCTGGGCCCAGCC[G/T]GAGGGTGATCACTTG | 9866 |
rs145631877 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682408 | CTGTGGAGGTGCGCG[A/G]GGCGGCTCAGGGCTG | 9866 |
rs145720631 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631624 | GAATGACCTCATACC[A/G]TGGCACTTTTCCAAG | 9866 |
rs145735913 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679715 | TGTCAAATAGACGAC[A/G]ATGTCTTCTTTGATC | 9866 |
rs145746130 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635973 | ATGAAACCACCTTTG[C/T]AAAAATTATATCAAT | 9866 |
rs145812634 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641887 | GTCCATGTGATGTGC[A/G/T]TCTTCACCTTCTGTC | 9866 |
rs145859471 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653437 | AAATCTAACCTGGCA[C/T]TGAGACTGCTGGAAG | 9866 |
rs145962285 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648961 | CGTGGATCATGAACT[C/G]TGGTTCCTGTGGATT | 9866 |
rs145983851 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652036 | AAATGAACTACACTT[C/G]ATGCCATAGCCTGCA | 9866 |
rs146040759 | in-del | -/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8629787 | GATTTATTTCCTTTT[-/C]CACAGCCACAGCCAA | 9866 |
rs146172964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8652872 | TGCTCCAGACTTATA[A/G]TCAGACAAATGTAAG | 9866 |
rs146271941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650132 | AACCCCAGTACTTTG[A/G]GAGGCCAAGGCAGGA | 9866 |
rs146325940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677506 | ACTAGGAGGCTGGGC[A/G]TGATGGTCATGCCTG | 9866 |
rs146326035 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628529 | AAGGTGGGAGGATTG[C/T]TTGAGCCCGGAAGGT | 9866 |
rs146391889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654230 | AATGCCCCTTGTAAA[C/T]TGACCTTATCTCTCT | 9866 |
rs146412396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644013 | TGTTTTCAGTTTAGT[C/T]ACCATACCTAGACCC | 9866 |
rs146512109 | snp | C/G | 0.00124146 | 0.0248835 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625249 | GGAACAGAGACAAGG[C/G]GTAGAGTCAGGCTGC | 9866 |
rs146539262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664205 | TAGTCATTCTGCAAC[A/G]TATCTATACTTCAAA | 9866 |
rs146633273 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644769 | CTTCTGTCTCTACTT[C/T]GTCACCACCCATCCT | 9866 |
rs146754521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665098 | TGCCATCCCTCTACC[A/G]GCTCCCACATTTTAC | 9866 |
rs146757523 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618662 | TCTTTTTGCACCACC[C/T]GAACAGCTTCACCTT | 9866 |
rs146758411 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670166 | TATAGGCACGCAACA[A/C]CATGCCCGGCTAATT | 9866 |
rs146775606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624267 | TGCTTCCCCAGCTTA[C/G]AGCTTGTCTGCTGGC | 9866 |
rs146878914 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641219 | CTTGCTACTTCCTGC[C/T]CCTGGGACAAAAGAA | 9866 |
rs146920368 | snp | G/T | 0.00171477 | 0.0292309 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671743 | AAACAGGAAGAGACC[G/T]GTTATGTAGTGGGAG | 9866 |
rs146936826 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675825 | TTCACTGCAACCTCC[A/G]ACTCCCTGGTTCAAG | 9866 |
rs146936911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626427 | AAAGCTATTTTGCCA[C/T]GAACACTGTCCTCAT | 9866 |
rs146966810 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630697 | AAACTGTGTGTCCCC[A/G]TCCCTGTCCCTTTCC | 9866 |
rs147006970 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8628630 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGAGAGAGA | 9866 |
rs147042429 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646633 | GAAGAGACAGCAAAC[A/G]TAAGAACCAACTTGG | 9866 |
rs147071914 | snp | C/G | 0.000192641 | 0.00981241 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649897 | GCAGTTCTGGAAGCA[C/G]AGAGTTCTGGAGTTA | 9866 |
rs147088164 | in-del | -/TGTG | 0.462253 | 0.132093 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625464 | CAAGCGGAGAACTAT[-/TGTG]TGTGTGTGTGTGTGT | 9866 |
rs147228866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648133 | GGGCTGAGTCCTACT[G/T]TGAGCATGCCAACCA | 9866 |
rs147307129 | snp | A/G | 0.000584715 | 0.0170885 | intron-variant, nc-transcript-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684255 | TCACGCTTGGGTATC[A/G]GCTATTGCCTGAGTG | 9866 |
rs147319775 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662490 | TGTCACTCTTCACTA[A/G]CTTCAAGAAGCATCG | 9866 |
rs147336543 | snp | C/T | 0.100231 | 0.200173 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668671 | GCTCACTGCAATCTC[C/T]GCCTCCCGGGTTCAC | 9866 |
rs147336691 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616265 | TCTCTCAGGTTGGGT[A/G]GAGAAGGAAATGAGC | 9866 |
rs147339755 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620786 | TGGGGTAGTAGTATA[C/G]GCACAAATCCACATG | 9866 |
rs147425225 | in-del | -/ACACACACACAG | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8625544 | ACCTGAGGCATGTAC[-/ACACACACACAG]ACACACACACAGACA | 9866 |
rs147426784 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8680023 | GTAAATTGCCAAGTG[C/T]TCTGAAAATGTTGGT | 9866 |
rs147443011 | snp | C/T | 0.000630151 | 0.0177392 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683281 | GTAAGTGCCGGCTTC[C/T]CCTCGGGGTGGGCCT | 9866 |
rs147531006 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623447 | AAGCAGGGTCTAAAA[A/G]GTTTAACTGCATAAA | 9866 |
rs147590161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634319 | CACAGGCATGCACCA[C/T]CACGCCTGGCTAATT | 9866 |
rs147606305 | snp | G/T | 0.000491232 | 0.0156644 | synonymous-codon, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8638705 | GCTGTCCACTGGGGG[G/T]ACACTGAGAGGGGTT | 9866 |
rs147693869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654130 | CAGAATGAAAAAAGA[G/T]AAAGAACTGAATAGG | 9866 |
rs147710148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8657781 | CTCAGAGCAGCACCA[C/T]CTTCAAGAAACATGT | 9866 |
rs147798665 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675493 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCCG | 9866 |
rs147816917 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678053 | AACTGGAAACTGTAC[A/C]TATTGCTGGTGAATA | 9866 |
rs147915507 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612341 | CCAGCTGTGTCCCAC[A/C]CCTGGAATTCCCCTG | 9866 |
rs147921300 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616894 | AGACTCACTTCTGAT[A/C]TTTGGCTCATGAACT | 9866 |
rs148041505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650937 | CAAGTATAGACCAGC[A/G]TTCAGAGTTGTGCTC | 9866 |
rs148079829 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613116 | GGGACTCAGGAAATA[C/G]AGAGACAGACAGAGG | 9866 |
rs148113002 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8679812 | GGGATGAAGACCATA[A/T]TGCTGTAAGGTCAGA | 9866 |
rs148166744 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676679 | GTTTCTGATTTGAGA[A/C]GACGAAGGGTCAAAT | 9866 |
rs148170281 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631960 | ATGCAATAGAAAAAG[A/G]GACCACAGATTTGGG | 9866 |
rs148220676 | snp | C/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8626308 | GGCATATCTATCTAA[C/G]TTTCCAAAATCAGTG | 9866 |
rs148271698 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648327 | CTTGGGCAGGGAGAA[A/G]ATTCTGATGCACGGG | 9866 |
rs148324567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642274 | AACAAGAGTAGGTGG[C/T]CATCAAAGGTCTGCT | 9866 |
rs148373861 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635626 | GAGTTCAAGCCATCA[A/G]AAGCCTATGAAACAC | 9866 |
rs148412655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655674 | CTGTAATCCCAGCCT[C/T]GGGAGGCCAAGGCAG | 9866 |
rs148416272 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643949 | TAACTAATGTCCCAA[C/T]GAACATCTTAGCCTC | 9866 |
rs148540079 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669317 | AATCAATGGTAATAC[C/T]TTGCATCCTCATTGT | 9866 |
rs148568946 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623534 | CAGTCAGTGTGAAAA[A/C]AAAGGAGAAAAATTA | 9866 |
rs148571255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654067 | TTCCACAAGACATCC[C/T]GGGTACCAGATGCCC | 9866 |
rs148626656 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680769 | GACCATGTACTGTGA[A/G]AAGATAAGGACAAGG | 9866 |
rs148661523 | in-del | -/TGTGTG | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8625464 | CAAGCGGAGAACTAT[-/TGTGTG]TGTGTGTGTGTGTGT | 9866 |
rs148678226 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677859 | AATTGCCATGTAGAA[C/T]ACTCTATCCAACACA | 9866 |
rs148694505 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633217 | ATCCCAGCTACTCAG[C/G]AGGCTGAGACAGGAG | 9866 |
rs148939556 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658550 | TGGTGAAGTGAGTAG[C/T]TGCAGGACCCTGGGG | 9866 |
rs148946372 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614951 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGTTCTGT | 9866 |
rs148946671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646298 | CCACCCTCCCAAAAT[C/T]AGGCTGACATTTTAA | 9866 |
rs149029437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676324 | ATCAGCAGTTTTACA[C/T]AACATTGCTTTGGCA | 9866 |
rs149079574 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670233 | GCCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 9866 |
rs149096175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625322 | GGAACTCCCATGCTC[C/T]AATTCCACTCTGGCT | 9866 |
rs149149890 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617819 | AAATGGCAAAGAAGA[C/G]CACTACACAGTTCAA | 9866 |
rs149157390 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8682211 | AAGAGAAAGGAAGCT[A/G]CAGTGCCCACTCAGA | 9866 |
rs149180904 | in-del | -/ATTT | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8674378 | TATTTCCTTTTTTCC[-/ATTT]ATTTATTTATTTATT | 9866 |
rs149207717 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649442 | TAAATAAATTAGAAG[G/T]GTAACATGATTACTC | 9866 |
rs149257219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620677 | CTGAGTCTCCGGCTT[C/T]GCCGTGTAAGAAATG | 9866 |
rs149314734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650290 | AGGTGGGAAGATCGC[C/T]TGAGCTCAGGAGGTC | 9866 |
rs149348045 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637937 | AGAGGTGAGAATAGA[C/T]AGTTGAGGATTTGTG | 9866 |
rs149406479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669029 | CAAAGGAAACAAATA[C/G]ACTTCACCTCTTGGT | 9866 |
rs149457647 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | TRIM66 | GRCh38.p7 | 11:8661807 | AACCACTCCCCCTTA[A/T]ATCAGAAAGTTCCAG | 9866 |
rs149474547 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615900 | ACCAGTTGCCCAACA[A/C]CAAGTACAACAAAGT | 9866 |
rs149559842 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677539 | ATCCCAGTGCTTTGG[A/G]AGGGCGAGGTAGGAG | 9866 |
rs149610829 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642046 | TCTTCACAATAATGC[G/T]AGAATGGACTAATAC | 9866 |
rs149612715 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673166 | ATCTCCTGACCTCAT[A/G]ATCCACCCGCCTCGG | 9866 |
rs149616214 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627295 | ACTGTTTATTCTACA[A/C]ATCTTTAGCCAAATG | 9866 |
rs149639839 | snp | A/C/T | 0.00156768 | 0.0279542 | intron-variant, nc-transcript-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684241 | CATCGAGGCTAGAGT[A/C/T]ACGCTTGGGTATCGG | 9866 |
rs149673439 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671370 | TCCTCCCTGCTGGGC[-/A]GCAGCTTAAATACTG | 9866 |
rs149715951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643901 | TTATCCAGGGCTTTG[A/G]CAAGTGTCCAACTTA | 9866 |
rs149721418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629991 | TATGTGTTAGTTATT[C/T]TTATACTATATCGGC | 9866 |
rs149859806 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653058 | CATGAATGTCAACTT[C/T]GGAGTTCAAAAGATT | 9866 |
rs149934556 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670173 | ACGCAACACCATGCC[C/T]GGCTAATTTTTGTAT | 9866 |
rs149987772 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663434 | TTTGTAAATTAGGCA[C/T]AGTAGGAGATTAACA | 9866 |
rs150017121 | snp | A/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617672 | CCGAGCCTAACCAGG[A/T]GTGGTCTTGTCAAGT | 9866 |
rs150074840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679070 | TCACAGAGAAGGACA[C/T]CCCTCAGGAGTCATG | 9866 |
rs150092709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634746 | ATCTCATTTTCAGCC[A/G]CAACCTGTTTCCACC | 9866 |
rs150093066 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666272 | TGAACCCGGGAGGCA[A/G]AGGTTCCAGTGAGCC | 9866 |
rs150122555 | snp | C/T | 0.0058707 | 0.0538598 | missense | TRIM66 | GRCh38.p7 | 11:8620456 | CCTACCTTCTGGTCA[C/T]ACATGCTTAGGCCAG | 9866 |
rs150176144 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614608 | AGCAAAGGCTCAATT[A/C]TGGCGTTCAGAAAGG | 9866 |
rs150233493 | snp | A/G | 9.40689e-05 | 0.00685752 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645917 | AAGACAGAGTCCTTG[A/G]TCCTGTTACTGGACT | 9866 |
rs150269400 | in-del | -/ACACACAC | 0.321053 | 0.23969 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622340 | GTACACACACACACA[-/ACACACAC]ACACACACACACACA | 9866 |
rs150385195 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TRIM66 | GRCh38.p7 | 11:8655035 | CTGGCTATTTTTGTA[C/T]TTTTAGTAGAGACAG | 9866 |
rs150498295 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8611590 | AGGCTGGGCGTGGTG[A/G]CTCACGCCTGTAATT | 9866 |
rs150620541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637537 | CCAGCAATTTCCAAG[A/C]TGACATTTCATTTTT | 9866 |
rs150672147 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632527 | GTCAGACGATCTCAG[C/T]TCACTGTAACCTCTC | 9866 |
rs150690853 | in-del | -/GT | 0.0766824 | 0.180169 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633500 | GACAGGCTTCTTAGA[-/GT]AGTGTGCTAAGTTCA | 9866 |
rs150760704 | snp | A/G | 0.00198452 | 0.0314376 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648376 | AAGTAAGAAATCCAG[A/G]GCCCTCCCCAGCCCA | 9866 |
rs150777212 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667191 | CATAATTCATTCACA[-/T]TAAAAACCTTAAATG | 9866 |
rs150814432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8642308 | TTAAATCAAAGGAAA[C/G]AGGGAAGAAAAGAAA | 9866 |
rs150852152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662975 | ACTTTCCAGACAGAA[C/T]TTGACCTGGGACCAT | 9866 |
rs150899245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672548 | AGGCTGGGTCACGCA[A/C]AAAGACAGATGGCAA | 9866 |
rs150916594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656741 | CCCCTTCCCCTGTGG[C/T]TGAGCCTGATAGCTG | 9866 |
rs150954630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678965 | TCATCTCTTCCGTTC[A/C]TTTCTGAGGTATTTT | 9866 |
rs151005644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674228 | ATTTACCACACTAGA[A/G]GTTAAAGCTGAGAAA | 9866 |
rs151022333 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629659 | TGAGCTGTGGAAAAA[C/T]TGCGGAAACTCCATG | 9866 |
rs151076339 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623993 | AGAGAACTGGTTTAC[C/T]AAATTCCATCTATCG | 9866 |
rs151136458 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680980 | TTTGGCAATTCGTTC[A/C]TTAATGACATTAGTA | 9866 |
rs151164601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639714 | TGCATATAAAACATA[C/T]CCAGCTTAGTAGAAG | 9866 |
rs151240328 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654282 | CCTAACATACAACCT[A/G]TGTTTTTGCCATGCC | 9866 |
rs151293452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649580 | CGAGAGTGAGTCACC[C/T]CTTTGACTCTGAAGG | 9866 |
rs180686073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623770 | GAACCAATCTCCAAT[A/G]GTCCAAATTGCCTTC | 9866 |
rs180693095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639901 | AGCCTCTCTTCTGCT[C/G]TGGCACTGGCAGGAG | 9866 |
rs180868887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656994 | GGCCTAGAGTGCAGC[C/G]TGAGGTTTGGCACTA | 9866 |
rs180874692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677128 | TAAGAATTTCAAAGA[C/T]TGTTTGCATGAAGGG | 9866 |
rs180912780 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635739 | AGATAGAATTCCTAG[A/G]ACCTTTGCTAACCCC | 9866 |
rs180963397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646079 | AGATGGTGGGAGATT[C/T]TATAGTGCAAATATG | 9866 |
rs180982458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683820 | GTAGCTGATATTACA[A/G]GTGTGCGCCACGACG | 9866 |
rs181191937 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8640112 | GGGCTGAGCTCAAGG[A/C]AGCCCTAAGGTGCAG | 9866 |
rs181199414 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631951 | TGTGTAAATATGCAA[C/T]AGAAAAAGGGACCAC | 9866 |
rs181201715 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8651253 | TCAGATACAGGAACA[A/G]GTAAGTAAATTAGTA | 9866 |
rs181210379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8670963 | ACTCATGAAAATATG[C/T]GTGTGGACCTCAGCT | 9866 |
rs181214519 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680926 | CAGATTAAAGTACAA[C/G]AGAAAGAACAAGTGA | 9866 |
rs181215857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, missense, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8663203 | CCTGAGAGGTGACGC[A/G]GACCCATCTTCCTAG | 9866 |
rs181241164 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8623907 | CCTAAGAAGTAGGTG[C/T]GATTGGCCCCATTTA | 9866 |
rs181255316 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613140 | ACAGAGGAAGCAGGA[C/G]CAGCTGTGATTCTTC | 9866 |
rs181419662 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675671 | ACAGGCATGAGCCAT[C/G]GCACCCGGCCTGCCA | 9866 |
rs181420918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628289 | ATTTCATCACTAAGT[A/C]GATTTGATGTAGATT | 9866 |
rs181422697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646663 | GAGGCTGCCTACTGA[A/G]ATCAGGGCCTAGCAG | 9866 |
rs181449870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655778 | CAGAGTGAGACTCTG[A/T]CTCCAAAAAAAATTA | 9866 |
rs181469742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618505 | AGCCCAGGTCTGCTG[C/T]TAAATGCTGGGTTAC | 9866 |
rs181598244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666940 | TGAGCCTCCCGAGTA[A/G]CTGGTGTCTGCCACC | 9866 |
rs181608218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634786 | CATAGCACCAACTCC[A/G]AGGTACTTGTACGCA | 9866 |
rs181608347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623308 | CTCCATGGAAAAGAG[A/G]CTCCCAGGGAGTTCT | 9866 |
rs181618770 | snp | A/C | 0.000162298 | 0.00900682 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8671891 | ATAGGAGATGAGAGC[A/C]CATACCTGGCAGGTC | 9866 |
rs181654225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652188 | TACTACAGGCCCAAC[A/G]CTGCTTTGGTTCTGA | 9866 |
rs181786857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632234 | AATTGCTTGAACCCA[A/G]GAGGCAGAGGTTGCA | 9866 |
rs181868702 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667722 | CTAAAGCTTCATCCA[C/T]GTTGTAGCATGTGTC | 9866 |
rs182002458 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8677048 | AAGAAAAGGAAAATA[C/T]TTACTGGAGTACCTT | 9866 |
rs182008544 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680488 | AACAGAGGAAGCACA[C/T]TGGGGAGATACAGAA | 9866 |
rs182024115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8661981 | CCATTACCGGGGGAA[C/T]TGCTCTCCCAGTAAT | 9866 |
rs182039928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635426 | TTGCTATCCTTGAGC[C/T]TCACACCCTCCACCC | 9866 |
rs182072012 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613378 | GGTGTGAAATGCTGC[A/G]GAGAGGTCAAGACAG | 9866 |
rs182277872 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678259 | GAATACAATAAGAAT[C/T]TTTTAAAAAAACAAA | 9866 |
rs182302114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638414 | TCTTTCCCTTCCTCC[C/T]TCCACTCTGCATGAA | 9866 |
rs182312454 | snp | C/G/T | 0.000119496 | 0.00772875 | intron-variant, missense | TRIM66 | GRCh38.p7 | 11:8618715 | TGCTTGCCTGATCAC[C/G/T]GCCCACCTGCTGCTG | 9866 |
rs182314597 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658986 | GATGCACAAAGGTCC[A/T]GGGAGGTCTCCCTTG | 9866 |
rs182315832 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614001 | TGGAAGCAGCAAATA[C/T]GATGATGCCGAAAAT | 9866 |
rs182316835 | snp | A/C | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653624 | CAGAGAATCCCAGCC[A/C]AAACAGCCAAACTGT | 9866 |
rs182329689 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656729 | TAGAGAGAGCATCCC[C/G]TTCCCCTGTGGCTGA | 9866 |
rs182334083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8652773 | ATCTGGAAAGGGGTT[A/G]GCTATGGCAGTGAAT | 9866 |
rs182426110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653301 | CTTTGAATCTAAGCT[C/T]ACCTTGTGACTTTCT | 9866 |
rs182430414 | snp | A/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8674515 | CTCCTAGGCAGCTAG[A/C]ACTATAGGCATGTGC | 9866 |
rs182452408 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8615703 | GAGCATGTGTCTCTC[C/T]AGCACATTACTAAGA | 9866 |
rs182455464 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633284 | CCGAGATCGTGCCAT[C/T]GCACTCCAGCCTGGG | 9866 |
rs182554306 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672974 | AGATGGAGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 9866 |
rs182576352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668206 | TGGGCTTATTGGTTA[G/T]TTGTACTTCATCTTT | 9866 |
rs182588960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632773 | CCCTCACATGTTGAT[G/T]TTTAATGGCAAAGTT | 9866 |
rs182604544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629189 | ATGTCTCCTTGTTGT[C/T]CTGGTTATGCACTAC | 9866 |
rs182647058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668986 | CCACATTCCAGTGGT[C/T]AAAGTAAGTCATAGA | 9866 |
rs182682954 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677469 | GCTATTTGTTCAATA[C/T]AATTCAGTGAGTAAA | 9866 |
rs182683034 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630365 | ACAGGAGGTGAATGT[C/G]TATTTCTAGCTATAA | 9866 |
rs182686320 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649265 | AATCGCTTGAACCCA[A/G]GAGGTGGAGGTTGTA | 9866 |
rs182859259 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682459 | AGACAACGAGGCCCT[A/T]AGGGTCGGCTTAGGC | 9866 |
rs182866429 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643815 | TGCAGGTAAAACACC[C/T]TTCTGTCCTACTCAA | 9866 |
rs182891116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648340 | AAGATTCTGATGCAC[A/G]GGGATTCCCAGAGCT | 9866 |
rs182896767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674772 | CCAAACCCTTTAACA[C/T]CTGGCTTAATAAAAG | 9866 |
rs183065153 | snp | C/T | 0.00680514 | 0.0579333 | missense, utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640460 | GGCCAGGAGGGCTCT[C/T]GTGCTGACTAGAAGC | 9866 |
rs183093376 | snp | C/T | 0.000187354 | 0.00967686 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624667 | GGCCAATCTTTTGCC[C/T]AATGATGAACAAAGG | 9866 |
rs183123275 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8665805 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 9866 |
rs183156516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8626925 | TCCTCACCCCCTTCA[C/G]ATGGACTGCTTTCTC | 9866 |
rs183165363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629683 | CTCCATGGCAGTTTA[C/T]TTTGAGGTGAACCTG | 9866 |
rs183168418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8657940 | GGCAACACTGGGAGA[A/G]AAGTCAGAGAAGCGA | 9866 |
rs183215687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620808 | ATCCACATGCAAGAA[A/G]AAGGTGAGAAAAGAG | 9866 |
rs183292804 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628729 | ACTCCCCTTCACTAT[A/C]TCTCATATTCTGTTC | 9866 |
rs183302092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647849 | CTTCTAGGACATATG[A/C]CCACATCTGCTTAAC | 9866 |
rs183308194 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621580 | GTCAGAATTCGGGCA[A/G]TAGCAGAAAGAATAA | 9866 |
rs183461998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636812 | CTGGAAGTCCTTCAC[C/T]TACTCCTCACATCCC | 9866 |
rs183477163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663676 | CATGTCAGAGACATA[C/G]CTGCACTCCCATGTT | 9866 |
rs183480941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634182 | GAGAGCTTTTCATTT[G/T]CTTAAGACAATCTCG | 9866 |
rs183509384 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681593 | CTATTAATAGACTAG[C/T]GAGGGGATGGGATCT | 9866 |
rs183534676 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8625453 | AGAGAGAGGCACAAG[C/T]GGAGAACTATTGTGT | 9866 |
rs183539145 | snp | A/C | 9.80344e-05 | 0.00700054 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8643022 | ACCAAGAGAAGCTAG[A/C]TGCTTGGTCCAGAAG | 9866 |
rs183545271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665501 | TGGCTGTCATTCATT[A/G]GACTATGAGCTCTTT | 9866 |
rs183685819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653825 | AAAAGAAAAACTTTC[C/T]GAGTTTTTGCAGAGC | 9866 |
rs183717821 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616095 | TCAAAGGGCAGAAGC[C/T]TAAGTCCAAAGATTG | 9866 |
rs183722083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637624 | AGACATGCATTGCAA[C/T]GGTACAGAGCTAGGG | 9866 |
rs183752287 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8677833 | AGTTTCCAATAAAGC[C/T]TTAGGAATGTAATTG | 9866 |
rs183779698 | snp | C/T | | | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622424 | GAACCCTGACTAATA[C/T]AATCCCCAGCTGAAT | 9866 |
rs183849094 | snp | A/C/G | 0.00128109 | 0.0252766 | synonymous-codon, missense, intron-variant, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640578 | AGGTGGTAGCTGCTG[A/C/G]TGTGGCTGCTGCTGA | 9866 |
rs183942175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658265 | GAGACCTCAAAGAGG[C/T]GACTCTCTTCCTAGC | 9866 |
rs184028425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634764 | ACCTGTTTCCACCAT[C/T]GGCTCACATAGCACC | 9866 |
rs184031898 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654542 | TCCTTCCAGTACAAC[A/G]AATATCACATTGCAT | 9866 |
rs184041013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675629 | TCAGATGATCCACCT[C/G]CCTTGGCCTCCCAAA | 9866 |
rs184059365 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617462 | CAAGCAAAGGCAAAC[A/T]GTGACAGTCTTTGGC | 9866 |
rs184268222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632076 | AAAATATGTGAATGC[A/G]CCGGGCATATCACCT | 9866 |
rs184277617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8651906 | CAGGAGATGAGCTCT[A/G]TGCAAGAAAGAAAGA | 9866 |
rs184282929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671637 | GGATTCACTCTGTCT[C/T]ACAGATTCCCCCAAA | 9866 |
rs184306562 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680509 | AGATACAGAAACAAA[A/G]GGATAGGGTGACAGT | 9866 |
rs184315721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666062 | ATATAAGAAGCTGGG[C/T]GCAGTGGCTCACTCC | 9866 |
rs184340979 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627743 | TTTGAATACTGACTT[C/T]GTATAGACCTTGCTA | 9866 |
rs184352269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645257 | AGGCACCTTAGATTC[A/G]AAGTATTCAAATATA | 9866 |
rs184371471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631303 | TATAAATTTCAGGTT[C/T]TTACAGCAAGATAAT | 9866 |
rs184453924 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650925 | ACCAAGGAAGGGCAA[A/G]TATAGACCAGCGTTC | 9866 |
rs184490667 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8612735 | AGTCTCCCTCCATCC[A/G]AATGTTATCAGCAGC | 9866 |
rs184552358 | snp | A/C/G | 5.84042e-05 | 0.00540363 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683921 | TCCTGACCTCAGGTG[A/C/G]TCTACCCCCCCTCGT | 9866 |
rs184567307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8650320 | CAAGGCTGCAGTGAG[C/T]CAAGATCGTACCACT | 9866 |
rs184569421 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623328 | CAGGGAGTTCTCCCC[G/T]GAGTATGCAGTCTAT | 9866 |
rs184573919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669566 | GAGAATCACTTGAAC[C/T]CAGGAGGCAGAGGCT | 9866 |
rs184584139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8639417 | ATGAAGATGTGAAAT[A/G]TAGCAAAGATCCCAG | 9866 |
rs184790741 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645481 | ACTACAGACTTTCCC[A/C]ACTGAGCTACCTTTG | 9866 |
rs184798927 | snp | G/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8666197 | CAAAAAAATTAGCTG[G/T]GCATGGTGGTGGGCA | 9866 |
rs184816442 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8683039 | GGCCCCTGCGCTACC[G/T]TGGTGAGACCTCACG | 9866 |
rs184902883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623103 | TGAACACAAGTAACA[C/T]TCAAGAGGCTGCCTA | 9866 |
rs184923711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8660988 | AGACTTGGAGGCCAT[A/G]CTAAGTGTCTGTTCT | 9866 |
rs184990820 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8679501 | GCAAACTATCCAAGA[A/G]GAGTGTCTTAGCACC | 9866 |
rs185022954 | snp | A/G | 0.000100801 | 0.00709863 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638632 | GTCCCATGTAGTTAG[A/G]GAAAACAGGCTCCTT | 9866 |
rs185032500 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8614578 | AAGAAGCCCAGGAAG[C/G]GGTGATCCAGAAGGA | 9866 |
rs185038700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662173 | GAGACTTGAGTTACT[A/G]CCCACAACAGACCCC | 9866 |
rs185071463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623778 | CTCCAATGGTCCAAA[C/T]TGCCTTCACTATGAG | 9866 |
rs185075363 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617126 | ACTTCTAGGAAGGCA[A/G]GTTCTCACCCTAAAG | 9866 |
rs185077986 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM66 | GRCh38.p7 | 11:8640081 | AGGTTGAGCCCAGCA[C/T]AGTTTTGAAATGTGA | 9866 |
rs185124084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8676673 | CAATGAGTTTCTGAT[C/T]TGAGAAGACGAAGGG | 9866 |
rs185153137 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634895 | AGGTTCTTCTGGTCC[A/G]TGACCTTCAGATAGA | 9866 |
rs185245303 | snp | A/G | 0.00261551 | 0.0360682 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682835 | GGTGTTTCGTTTCTT[A/G]CCTCCTCTTCCTTGC | 9866 |
rs185264713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618521 | TAAATGCTGGGTTAC[C/G]CTGGGCAGGGACAGG | 9866 |
rs185271754 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8657520 | TGTATAACATAGGTG[A/T]TACCGTGAACTACTA | 9866 |
rs185282082 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8655820 | AAAAATTAAAAAAAA[A/T]ATATTCTCTTGGGCA | 9866 |
rs185282534 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677319 | GGACTTTTGTTCACA[A/G]TTGTACCTGCCCCTC | 9866 |
rs185302569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8620283 | AGAGGAAAACTGCTA[A/G]GAGAAGGAAAATTAT | 9866 |
rs185312503 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635770 | ATTGCCAACTTGCAG[C/G]CACACAAAAGGGCAG | 9866 |
rs185400906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8680403 | AGGCAGAGTGAACAA[A/G]GGAAGGTGTTGTAAA | 9866 |
rs185440241 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8611771 | CTGAGGCAGGAGGAT[C/T]GCTTGAACCTGGAAG | 9866 |
rs185515810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8661701 | TCAGCAGGATCCTAG[A/C]CCTTCCTGGACTCCT | 9866 |
rs185585307 | snp | A/C | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8630556 | GTCAAAATGCCAAAA[A/C]ACATTCACTCTGATA | 9866 |
rs185690778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654401 | TTCTTGCCCCTCTCC[C/T]TTTCAGATAAACTCC | 9866 |
rs185692937 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627954 | CCACCTCAGCCGCCA[G/T]AGTAGCTGGGACTAC | 9866 |
rs185816221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634367 | AGAGACTGGGTTTCA[C/T]CATGTTGCCCAGGCT | 9866 |
rs185829933 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675396 | CTGCCAGTTATTCTT[G/T]TTTTAGATGCAGTTT | 9866 |
rs185844139 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613170 | CCTCCCTACCCAACT[A/C]CTGAAAAGAAGAGAC | 9866 |
rs185886471 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8673095 | CAGGCACCCACCACC[A/G]CCCTGGCTAATTTTT | 9866 |
rs185898942 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675285 | AATTCTAACTTTTGC[C/T]TGAACGCTTGAATTT | 9866 |
rs185922746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632820 | ATGAGTGTTCCTCCA[C/T]CTCAAGAGAAAGCTC | 9866 |
rs186017172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8684496 | TGCCTCTGACATTGT[C/T]GGTGGTTTATCCTGG | 9866 |
rs186050988 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8628290 | TTTCATCACTAAGTA[A/G]ATTTGATGTAGATTT | 9866 |
rs186057148 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8647173 | GAAAATGTTTTAAAC[A/G]TAGACAGTAATTATG | 9866 |
rs186059608 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8652834 | CATCTCTTCAAAATA[C/T]GAAAGAATGATATGA | 9866 |
rs186065310 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667191 | CATAATTCATTCACA[A/T]TAAAAACCTTAAATG | 9866 |
rs186070916 | snp | G/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8623022 | ATAGTCATTCATACA[G/T]AGTGGTGACAAGTCT | 9866 |
rs186181468 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8646364 | TATCTGAATTACAGC[C/G/T]TAGGCTTCCCTAGGT | 9866 |
rs186263364 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681355 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 9866 |
rs186286656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8672120 | GTGAAGCACAAAGCA[A/G]AGTGATCTACTTATT | 9866 |
rs186289018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8641187 | AGTTTTTCAAAAGTT[C/T]TTCAAGTTGCTCCCA | 9866 |
rs186292681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8664042 | AGTTAGATAGCAGGA[C/G]TCAGTTCAAGAGATC | 9866 |
rs186311122 | snp | A/G | 0.000170547 | 0.00923278 | intron-variant | TRIM66 | GRCh38.p7 | 11:8624706 | ATAGCATTTCCCCAG[A/G]ACTTACCTTACACAG | 9866 |
rs186343848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8666538 | CTTCTTTCTATAAAC[A/G]AGGCATAGTACAGAA | 9866 |
rs186374889 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8627999 | ACATTGGCTAACTTT[C/T]ATTTTTTATTTTTGT | 9866 |
rs186381178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8619070 | AGCCTAGCGGGGTGT[C/T]CTGAGGTGTCTGGAA | 9866 |
rs186384147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8635461 | CAACCCCAGCTCCAA[A/G]GCAACAAATTTCCTC | 9866 |
rs186459084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8663229 | CCTAGTTGCTGGGGA[A/G]AATCTCAGCTAGGCT | 9866 |
rs186485918 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8623974 | TACCCGGGATCACAG[G/T]GAGAGAGAACTGGTT | 9866 |
rs186515518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8667794 | ATGTATATACCACAT[G/T]TTGTTTATCCATTCA | 9866 |
rs186613582 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681043 | CTAGACCGCAGTGAA[C/T]AATGGATGGGAAGGT | 9866 |
rs186647394 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TRIM66 | GRCh38.p7 | 11:8640395 | GTCCTTCTGCATTTC[C/T]TCCAGCTCAAACTTG | 9866 |
rs186685858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634602 | GGTTGTAGCCATGGT[A/C]TTTCTTTCAGAGTGG | 9866 |
rs186693847 | snp | A/G/T | 0.00239369 | 0.0345212 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677543 | CAGTGCTTTGGGAGG[A/G/T]CGAGGTAGGAGGGCT | 9866 |
rs186703261 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8654420 | CAGATAAACTCCTAT[G/T]CATCCTTTCATACCT | 9866 |
rs186735122 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8643362 | TTTTTTTAATTGAGA[C/T]GGGGTCTCACTCTGT | 9866 |
rs186739170 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681594 | TATTAATAGACTAGC[A/G]AGGGGATGGGATCTT | 9866 |
rs186740988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8665525 | GCTCTTTGAAGTCAA[A/G]GGCTCTGTCTTTTCA | 9866 |
rs186745011 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8617319 | CACCTATGTCAACAT[C/G]AGGAAAGTGACTATG | 9866 |
rs186901004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8658036 | ATGCTGCAGCCAGGC[A/G]GGCTGCAAGGCCTAA | 9866 |
rs186940496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8678706 | CTTAAAAAAGAAAAC[A/G]AACATATTTCCAAAT | 9866 |
rs186970117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8638457 | CCATTTTAAGTGTGC[A/G]TGGGGGAGTGGAAAT | 9866 |
rs186976771 | snp | A/T | | | upstream-variant-2KB, intron-variant | TRIM66 | GRCh38.p7 | 11:8659885 | CTTGTTTGTTTGTCT[A/T]TGTTTGTTTTGAGAC | 9866 |
rs187006790 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613706 | ACAACAGGATTCAAG[A/C]TATAGAGAATTAAAT | 9866 |
rs187017109 | snp | A/G | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8652408 | AAGGCCTCCCTGCCC[A/G]CTCATCTAGGAGGTA | 9866 |
rs187061530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653637 | CCCAAACAGCCAAAC[A/T]GTAGAATCATAAAAT | 9866 |
rs187071710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674646 | CCATTTTGGCCGCCC[G/T]AAGTGCTGGGATTAT | 9866 |
rs187087336 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616034 | AAGGAGATTCAAAAA[C/T]TGAAAGGGAAATGAC | 9866 |
rs187097827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8633419 | GGACCTGTTTTCTCA[C/T]GGGCCAGGAGACCTA | 9866 |
rs187220603 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632564 | CTAAGTTCAAGTGAT[G/T]CTCCTGCCTCAGCCT | 9866 |
rs187286975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8649563 | CCATCAACAGGGAGG[A/G]ACGAGAGTGAGTCAC | 9866 |
rs187291530 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669071 | CAGAAAAGAATTGTG[G/T]CCATCTTTAAATCCC | 9866 |
rs187295021 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8656763 | TGATAGCTGTCTCCT[A/G]TATCATGCAGCTGAG | 9866 |
rs187314899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8630488 | ATGAAGGAAAAGGTA[C/T]ATTTTGAGATTCACT | 9866 |
rs187454994 | snp | G/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8629687 | ATGGCAGTTTATTTT[G/T]AGGTGAACCTGATGA | 9866 |
rs187535616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675444 | CTGGAGTACAATGGC[A/G]TGATCTTGGCTCATA | 9866 |
rs187562070 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8677104 | AGTCATTCCACATCA[C/T]ATTGGGAATAAGAAT | 9866 |
rs187565197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8647909 | GACGGCCTGGTGTTG[G/T]AACCCTGGGTGTGCG | 9866 |
rs187765851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8622754 | AGGATGCTTCATCCC[C/T]GTGCCAGCATCTCAG | 9866 |
rs187779883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8640129 | GCCCTAAGGTGCAGA[A/G]ACTGTATTCCTGTGC | 9866 |
rs187791852 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8625750 | GGGGTTGAGAAGGCT[C/T]AAACTCTTATCTGCC | 9866 |
rs187801564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8648991 | TTGACAGTTGTAGAA[A/C]CCCTCCCACAATTCA | 9866 |
rs187945590 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM66 | GRCh38.p7 | 11:8637741 | TGGGAGAGTTCAGAA[A/C]ACCTGACAGAGCTTC | 9866 |
rs187956175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8658393 | GCACAGCTCGGGAGA[C/G]AGCACTCTCAGCCTT | 9866 |
rs187988658 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8621633 | TAAGGCCAAGGCAAA[G/T]CAAAGTGGTACCTTA | 9866 |
rs188007301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RPL27A, SNORA3A, SNORA3B, TRIM66 | GRCh38.p7 | 11:8683557 | GGAATCCTAAAGTAA[C/T]CGCATTGCTGAAAAC | 9866 |
rs188008321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8665911 | CCGAGATCTCACCAC[C/T]GCACTCCAGCCTGGG | 9866 |
rs188013262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8677112 | CACATCACATTGGGA[A/G]TAAGAATTTCAAAGA | 9866 |
rs188041089 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM66 | GRCh38.p7 | 11:8627322 | AATGAACAGCAGCTT[A/T]GGTCTACTGACAACT | 9866 |
rs188043865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8668822 | AACTCCTGAGCTCAG[A/G]TAATCCGCCCACCTC | 9866 |
rs188063110 | snp | C/T | | | intron-variant | TRIM66 | GRCh38.p7 | 11:8625356 | GAGTCTGGTAGCTGC[C/T]GGTAGCTGCCAGGAA | 9866 |
rs188072167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8629570 | CATATTCGTGGGAAA[C/T]TGGCTCTCCTGTCCT | 9866 |
rs188258982 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8680837 | CAACGCTGGATGGAA[C/G]AACCTGAAAAGAAGA | 9866 |
rs188278000 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | RPL27A, SNORA3A, TRIM66 | GRCh38.p7 | 11:8682472 | CTTAGGGTCGGCTTA[A/G]GCGGTTCCCTGACCA | 9866 |
rs188285004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8662622 | GAGCTCTAGGGTCTG[C/T]GACTTCCAGCTACAT | 9866 |
rs188303830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8636994 | ACTTCTGAAGCTCCC[C/T]AGTTGCCATTCCTTT | 9866 |
rs188328701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM66 | GRCh38.p7 | 11:8644717 | TCCCCCAACTCTGCC[A/G]TCTTCTCAGGCTATG | 9866 |
rs188435414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8631513 | GCTAAGGAGACCATT[C/T]CTTAGTGATATCAAG | 9866 |
rs188468183 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613023 | GAGAGACAGAGGGAA[A/G]GACTCACAGATGCTG | 9866 |
rs188559719 | snp | C/T | | | intron-variant, utr-variant-5-prime | TRIM66 | GRCh38.p7 | 11:8653986 | CTCTCTTCCACTTGG[C/T]TCACCCTGAGGTGAC | 9866 |
rs188593976 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8616311 | CAAAGAGAGAAGAAA[C/T]GTTTTCTAATTAAAA | 9866 |
rs188625116 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | TRIM66 | GRCh38.p7 | 11:8620967 | CTGTGGGCCTGGCCT[A/G]GAATAATCATCCCTG | 9866 |
rs188678720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8675642 | CTGCCTTGGCCTCCC[A/C]AAGTGCTGGGATTAC | 9866 |
rs188712893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634765 | CCTGTTTCCACCATC[A/G]GCTCACATAGCACCA | 9866 |
rs188719188 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRIM66 | GRCh38.p7 | 11:8654918 | CAGGGTGGACTGCAG[C/T]GGCACAATCTCGGCT | 9866 |
rs188722942 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM66 | GRCh38.p7 | 11:8628150 | ATGGTAAATCTATTT[C/T]TTTTTCTTTACATTT | 9866 |
rs188745891 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM66 | GRCh38.p7 | 11:8618119 | TTTATTCTACCCTAG[A/G/T]AATGCAGCAGTAAAA | 9866 |
rs188813148 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM66 | GRCh38.p7 | 11:8669805 | AGTAATCAGCCCTCT[C/G]CTCTGCCCTTAGGCA | 9866 |
rs188847852 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM66 | GRCh38.p7 | 11:8674980 | TAGTAGTTTCTTAAA[A/T]GTTATTTATAAGGTA | 9866 |
rs188876711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8634242 | GCAATCTCGGCTCAC[C/T]ACAACTTCCGCCTCC | 9866 |
rs188950612 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TRIM66 | GRCh38.p7 | 11:8632119 | TCGAGACCAGCCTGA[C/T]CAACATGGCAAAACC | 9866 |
rs188960884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8652043 | CTACACTTGATGCCA[C/T]AGCCTGCATTTAGTA | 9866 |
rs188971464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM66 | GRCh38.p7 | 11:8671750 | AAGAGACCTGTTATG[G/T]AGTGGGAGGTGAACT | 9866 |
rs188994966 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM66 | GRCh38.p7 | 11:8613242 | ACAGCTCAGCCTGTG[C/T]GGGCTGAGAGGTAAG | 9866 |
rs189027045 | snp | A/G | | | upstream-variant-2KB, intron-variant | RPL27A, TRIM66 | GRCh38.p7 | 11:8681652 | GAGCGAAGACATGCT[A/G]CTATTAGCGAAGACA | 9866 |
rs189048528 | snp | A/C | 0.000280807 | 0.0118459 | intron-variant | TRIM66 | GRCh38.p7 | 11:8645907 | GTACAGAGAGAAGAC[A/C]GAGTCCTTGATCCTG | 9866 |