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 |