SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13556 | snp | A/G | 0.291154 | 0.246589 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696743 | TTCTCTGCCGGCCCC[A/G]CCTCTGCTGGGAGCA | 115992 |
rs752843 | snp | C/T | 0.447162 | 0.153712 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702696 | TCGTGTGAGAGAAAG[C/T]GGGACTCAGCTTGAG | 115992 |
rs753285 | snp | A/G | 0.478437 | 0.10157 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703626 | CTTCCTGTGGGGGAA[A/G]CGGGCACTACTCCCG | 115992 |
rs753286 | snp | C/T | 0.465263 | 0.127129 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703602 | ACTCCCGGCTGCTGG[C/T]TCTCTGAACACCAGG | 115992 |
rs877578 | snp | A/C | 0.108755 | 0.206276 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88704169 | GGGGACAGAACCAGA[A/C]CAGCAACAAACTTCC | 115992 |
rs877579 | snp | C/T | 0.307671 | 0.243257 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88704213 | AGAGCCTTTAAACTT[C/T]CTGTGGTCATTTGCA | 115992 |
rs880233 | snp | C/T | 0.451856 | 0.147493 | upstream-variant-2KB, utr-variant-5-prime | CTU2, RNF166 | GRCh38.p7 | 16:88706407 | CGCTACTGCGCCGCG[C/T]TGACGTCATCGTAGG | 115992 |
rs880234 | snp | C/T | 0.247884 | 0.249991 | utr-variant-5-prime, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88706520 | AGTCTGCGACGGGAC[C/T]CGGCGTGCCCATGTG | 115992 |
rs881633 | snp | A/G | 0.186421 | 0.24178 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707330 | GAGGGACCCCATCAG[A/G]AGCAGGAATAAAGTA | 115992 |
rs1052947 | snp | C/T | 9.9985e-05 | 0.00706983 | intron-variant, utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | RNF166 | GRCh38.p7 | 16:88701346 | CTGCCGCCTGCCCTT[C/T]GACCCCAAGAAGGTG | 115992 |
rs1132572 | snp | A/G | 0 | 0 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696732 | GAGGCGGGGCCGGCA[A/G]AGAAGGGGCCTCCTC | 115992 |
rs1132574 | snp | A/G | 0 | 0 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696730 | GGCGGGGCCGGCAGA[A/G]AAGGGGCCTCCTCCA | 115992 |
rs1132576 | snp | C/G | 0 | 0 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696663 | AGCTGACTGTGCCCC[C/G]CTGCGGGAGGGGACG | 115992 |
rs1132579 | snp | A/T | 0.499867 | 0.00815663 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696535 | TTGCTGTCTTTTTTT[A/T]AAAAAAAAAAGTTTA | 115992 |
rs2306048 | snp | C/G | 0.494691 | 0.0512477 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88701453 | TTCGGGAGACCCGAG[C/G]GGCGGGCTGGCACTC | 115992 |
rs2306049 | snp | C/G | 0.499718 | 0.0118813 | intron-variant, utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | RNF166 | GRCh38.p7 | 16:88701361 | CCCGCTGTGCCCACT[C/G]TGCCGCCTGCCCTTC | 115992 |
rs2340970 | snp | C/G | 0.289424 | 0.246872 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700565 | TGTGAGCGCTTCATA[C/G]AACTTATTCACCTGA | 115992 |
rs2340971 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702623 | TCCCCCAGGCCCTCT[C/T]TGCCACCACTGGATT | 115992 |
rs2340972 | snp | A/G | 0.249603 | 0.25 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703142 | CCACTCACGCTCAAC[A/G]TCCAGCAGAGAGAAA | 115992 |
rs2340973 | snp | A/G | 0.186737 | 0.241863 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88706988 | CTTGAAGTTTGGACA[A/G]AACACAAGCCTGGGT | 115992 |
rs2879899 | snp | A/G | 0.298905 | 0.24517 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88697488 | AGTCCGGTGAGGTGC[A/G]CTCCCGAGCAGGTGC | 115992 |
rs2879900 | snp | A/C | 0.48155 | 0.0942576 | intron-variant, missense | RNF166 | GRCh38.p7 | 16:88699987 | AGAAGGGTAGCGGGA[A/C]ACAGGTAAGGAGATC | 115992 |
rs2879901 | snp | A/G | 0.43221 | 0.171171 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703296 | ACGACTGGATGGTGC[A/G]CCTCCTGAGTGAACC | 115992 |
rs3209430 | snp | A/G | 0.0111108 | 0.0737016 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696747 | TGGCTGCTCCCAGCA[A/G]AGGCGGGGCCGGCAG | 115992 |
rs4238683 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88705208 | CCAGCACACATCCAC[C/T]TAGCAGTCCCAGCTC | 115992 |
rs4489989 | snp | G/T | 0.473451 | 0.112115 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703257 | AATTGCATCGATTGT[G/T]GCATAATTGCAAACA | 115992 |
rs4597303 | snp | C/T | 0.0748431 | 0.178382 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88697153 | TGCGCAAGGTGGAAG[C/T]GGGGCCGGGGCAGGG | 115992 |
rs4643303 | snp | C/G/T | 0.106278 | 0.204558 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88705221 | ACCTAGCAGTCCCAG[C/G/T]TCCCTCTGTACCAGG | 115992 |
rs4644850 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88706998 | GGACAGAACACAAGC[C/T]TGGGTTTGTGTGTGT | 115992 |
rs4782318 | snp | A/G | 0.497586 | 0.0346604 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702992 | GTCGGTAAACGGATG[A/G]AGAGACGGCGTGGCG | 115992 |
rs4782425 | snp | C/T | 0.25912 | 0.249834 | intron-variant, upstream-variant-2KB | RNF166 | GRCh38.p7 | 16:88701060 | CCGGGCTGGCCCCCC[C/T]GTCAGCCGTCACCAC | 115992 |
rs6500489 | snp | C/T | 0.141596 | 0.225274 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88705638 | AGTGATCGGTGTGAC[C/T]CAAGTTCTCCTTCAA | 115992 |
rs6500490 | snp | A/C | 0.44858 | 0.151875 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707345 | CCTGATGGGGTCCCT[A/C]GTGCCCCTGGTGTTG | 115992 |
rs7185382 | snp | A/G | 0.143959 | 0.226396 | intron-variant, missense | RNF166 | GRCh38.p7 | 16:88700144 | CCGTGGAGGCAGGGC[A/G]CCATCCTCCACCCAC | 115992 |
rs7194105 | snp | A/G | 0.315516 | 0.241263 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88706083 | GCGCGCCCAGTCCGG[A/G]GCTGCACCGGGGCGG | 115992 |
rs7196734 | snp | A/G | 0.145642 | 0.227177 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88701527 | GGGGTCCACAGGGGC[A/G]GCTCCCCCTACCGCT | 115992 |
rs7201334 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF166 | GRCh38.p7 | 16:88698891 | ACCCCCGGACTCGCC[A/G]CGAGCAGGCTCCTGG | 115992 |
rs7350860 | snp | C/T | 0.307919 | 0.243198 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703001 | CGGATGGAGAGACGG[C/T]GTGGCGTGCACACCC | 115992 |
rs11076700 | snp | C/T | 0.352209 | 0.228152 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88697550 | GGAAGCGCAGCCACC[C/T]GCCTGCGTCTGGGGT | 115992 |
rs11076701 | snp | A/G | 0.198324 | 0.244601 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88708117 | CCACACCTGGCCAAG[A/G]TAGGTACTTCTTTAA | 115992 |
rs11076702 | snp | A/C | 0.154993 | 0.231244 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88708161 | TCTGAAATTGCCAAG[A/C]ACACCAGGCTGCCGG | 115992 |
rs11395253 | in-del | -/T/TTGT/TTGTT | 0.210301 | 0.246828 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707812 | TTGTTGTTGTTGTTG[-/T/TTGT/TTGTT]TTTTTTTTGAGATGG | 115992 |
rs11640063 | snp | C/T | 0.343254 | 0.231956 | intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700882 | CCTTGACTGTGCCCG[C/T]GGCCCTTGTGACCTT | 115992 |
rs11641194 | snp | A/C | 0.344554 | 0.23155 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707120 | TTCTCTCTTCTCCCC[A/C]CTCCCATCTCCAAAG | 115992 |
rs11641365 | snp | C/T | 0.340559 | 0.233022 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707485 | GCCGTGGTGTCTAGA[C/T]TGGGATAAGCTGTAG | 115992 |
rs11644923 | snp | G/T | 0.35207 | 0.228214 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702274 | ACTGGGGCAGCCACA[G/T]CTGGCCTTGTGAGGA | 115992 |
rs11648894 | snp | C/T | 0.271972 | 0.249033 | intron-variant, missense | RNF166 | GRCh38.p7 | 16:88699951 | GCAGGACAATCTGGC[C/T]GAGGGCAGAAACCTG | 115992 |
rs11649075 | snp | C/T | 0.267091 | 0.249415 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700332 | ACCCAGATTAGAGAA[C/T]GGAGCTGCTGTGGGA | 115992 |
rs11649077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700358 | TGGGATACGGGAGGC[C/T]GCTCTGCATGTGACC | 115992 |
rs11649140 | snp | C/T | 0.274929 | 0.248754 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700532 | TCGAGGACAAACCAC[C/T]GAGGGGCCACGTACT | 115992 |
rs11649186 | snp | C/T | 0.317692 | 0.240661 | intron-variant, utr-variant-5-prime, missense | RNF166 | GRCh38.p7 | 16:88700637 | AGCTGCTCAGTCCTC[C/T]GGAAGCCACTGAAAG | 115992 |
rs11649226 | snp | C/T | 0.38286 | 0.211774 | intron-variant, utr-variant-5-prime, missense | RNF166 | GRCh38.p7 | 16:88700709 | TGCCAGGGAGGGCCA[C/T]GGGGCACGGGCCAGG | 115992 |
rs11863597 | snp | A/C | 0.333952 | 0.235483 | downstream-variant-500B | RNF166 | GRCh38.p7 | 16:88696098 | AGAAACCAATCCAGG[A/C]GGTGCTGAGGTGGCG | 115992 |
rs12922883 | snp | G/T | | | upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88706435 | AGGGCGCCGCCCCCA[G/T]CCGGGCTTCGCGGCC | 115992 |
rs28685172 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707576 | AACTTGGCAGATGGT[C/G]TGGGTGAAAGTTTTT | 115992 |
rs34261805 | in-del | -/G | | | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88697256 | TCTTCCCACGAGGGG[-/G]TATCATGGCTTTGAA | 115992 |
rs34338905 | in-del | -/T | | | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696774 | CCACAGCCTGTGGCT[-/T]GGGGTGCTGGGATTT | 115992 |
rs34760068 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707819 | GTTGTTGTTTTTTTT[-/T]GAGATGGAGTCTCCC | 115992 |
rs34809978 | in-del | -/G | | | intron-variant | RNF166 | GRCh38.p7 | 16:88699089 | TTGGGGATGTTGCTG[-/G]CGGGGCGGGGGTAGA | 115992 |
rs35018384 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88705025 | AGAGGCTGCCCCCCC[-/C]AAAATGTCACGGCTA | 115992 |
rs35287909 | in-del | -/C | | | intron-variant | RNF166 | GRCh38.p7 | 16:88698804 | TCATGGACACTCCCC[-/C]GGTTTCCGCCAGGTG | 115992 |
rs35399727 | snp | C/T | 0.0916144 | 0.193427 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703091 | GAAAACAGTGCAGGG[C/T]AGACAGCAAGCACGT | 115992 |
rs35639468 | in-del | -/T | 0.402083 | 0.198421 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696525 | ACATTTTATTTAAAC[-/T]TTTTTTTTTAAAAAA | 115992 |
rs45440295 | snp | A/T | 0.305685 | 0.24372 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703816 | CACACTGGCCGCTGC[A/T]CAAGCTGAGAAGCTG | 115992 |
rs45507504 | snp | A/G | 0.165853 | 0.235413 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703180 | ACCAGAAAGCAGACG[A/G]GTGGGTGCCAGGCGA | 115992 |
rs45615138 | snp | A/G | 0.281841 | 0.247964 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703906 | ACAGCTGTCCTGCAC[A/G]AGTGGAGGCTGCTCA | 115992 |
rs55780854 | snp | C/T | 0.402039 | 0.198454 | intron-variant, missense | RNF166 | GRCh38.p7 | 16:88699760 | GCAGGGAGGGCAAGG[C/T]GGTCCTGAGAATCTG | 115992 |
rs57506951 | snp | A/C/G | 0.0291713 | 0.117543 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88704626 | ACAAGGCCTAAGTCA[A/C/G]GCCTCACAGCGCTCA | 115992 |
rs57626073 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88701856 | AAAACCTCAAACAAT[C/T]GTGGGAAAGGAAACG | 115992 |
rs57817451 | snp | C/T | 0.199564 | 0.24486 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88708144 | TTAACCACCCAGGAG[C/T]ATCTGAAATTGCCAA | 115992 |
rs57865118 | snp | C/T | 0.0854556 | 0.188216 | intron-variant, upstream-variant-2KB | RNF166 | GRCh38.p7 | 16:88701046 | CAGTGCTACCCCCAC[C/T]GGGCTGGCCCCCCCG | 115992 |
rs57958330 | snp | G/T | 0.184521 | 0.241273 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707006 | CACAAGCCTGGGTTT[G/T]TGTGTGTACCGAGGT | 115992 |
rs58500305 | snp | G/T | | | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707500 | CTGGGATAAGCTGTA[G/T]GAGGACCAGGCGTTT | 115992 |
rs58769233 | snp | A/G | 0.00279078 | 0.0372506 | intron-variant | RNF166 | GRCh38.p7 | 16:88697666 | AGATGCACCGGGCTC[A/G]AGGGAGACAGGAAGG | 115992 |
rs58797132 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88708066 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 115992 |
rs59253789 | snp | A/G | 0.212122 | 0.247114 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703135 | TGGGGGTCCACTCAC[A/G]CTCAACGTCCAGCAG | 115992 |
rs59745254 | snp | C/G | 0.0984431 | 0.198823 | upstream-variant-2KB, intron-variant | CTU2, RNF166 | GRCh38.p7 | 16:88704514 | TTTGAAAAAGAAGGG[C/G]AAAGACCAATTTGTG | 115992 |
rs59925960 | snp | A/G | 0.106987 | 0.205054 | intron-variant, upstream-variant-2KB | RNF166 | GRCh38.p7 | 16:88704460 | TCCATGTGGTTCTGC[A/G]TTCTGTGTTATGGAA | 115992 |
rs60649326 | snp | C/T | 0.135484 | 0.22223 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703104 | GGCAGACAGCAAGCA[C/T]GTCCCACCCGTGTCG | 115992 |
rs61730430 | snp | A/T | 0.000497273 | 0.0157604 | missense, upstream-variant-2KB, utr-variant-5-prime | CTU2, RNF166 | GRCh38.p7 | 16:88707186 | AGCCCGTTGTGGTGA[A/T]ACGAGCCGGAGATGC | 115992 |
rs61742248 | snp | A/G | 0.0158173 | 0.0875127 | synonymous-codon, missense | RNF166 | GRCh38.p7 | 16:88698574 | GCTCTTGTAGCTGGG[A/G]TCCCCCCAGGGCATT | 115992 |
rs62623396 | snp | C/G | 0.00136978 | 0.0261345 | intron-variant, missense | RNF166 | GRCh38.p7 | 16:88699759 | GGCAGGGAGGGCAAG[C/G]CGGTCCTGAGAATCT | 115992 |
rs66593397 | in-del | -/CCTCCTGCTGCTATCTACAACCG | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702154 | TTGGGCTCGCACACC[-/CCTCCTGCTGCTATCTACAACCG]CTCCCGCTCTGCAGA | 115992 |
rs71158748 | in-del | -/TGCTGCTATCTACAACCGCCTCC | 0 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702158 | GCTCGCACACCCTCC[-/TGCTGCTATCTACAACCGCCTCC]CGCTCTGCAGACGCA | 115992 |
rs71395317 | snp | A/G | 0.0479149 | 0.147179 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703121 | TCCCACCCGTGTCGT[A/G]GGGGTCCACTCACGC | 115992 |
rs73260597 | snp | A/G | 0.0854556 | 0.188216 | downstream-variant-500B | RNF166 | GRCh38.p7 | 16:88696049 | GTGGCCCCTCAGAGA[A/G]CTACAGGCAGTTAGT | 115992 |
rs73260600 | snp | C/T | 0.0376037 | 0.131863 | utr-variant-3-prime | RNF166 | GRCh38.p7 | 16:88696909 | GCAGCTGCCCCACTG[C/T]TCCTTCCATCCTTGC | 115992 |
rs73262612 | snp | A/G/T | 0.0850919 | 0.187897 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702261 | GAAGGAGCTTAATAC[A/G/T]GGGGCAGCCACATCT | 115992 |
rs74033349 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88700795 | TTACGCTGCTCTGAT[A/G]TGGGTGTGGCAGTGC | 115992 |
rs74033350 | snp | A/G | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88701764 | CGTTCACGTGGCGAC[A/G]ACACCTGGGTGGGCT | 115992 |
rs74525506 | snp | C/T | 0.0633504 | 0.166319 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702794 | CGAGTTCTCACCAGG[C/T]GCCCCAGCAGATATT | 115992 |
rs75142100 | snp | C/G | 0.0341408 | 0.126114 | downstream-variant-500B | RNF166 | GRCh38.p7 | 16:88696041 | CCCTGGTGGTGGCCC[C/G]TCAGAGAACTACAGG | 115992 |
rs75387247 | snp | A/G | 0.5 | 0 | intron-variant | RNF166 | GRCh38.p7 | 16:88698637 | CTGGGGTCAAGCCGA[A/G]CCGGACCGCGGAGAG | 115992 |
rs75410747 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703350 | GGGCTCGGCTGCACA[A/G]CACGGCCACGGGCTG | 115992 |
rs75746195 | snp | A/G | 0.209984 | 0.246777 | intron-variant | RNF166 | GRCh38.p7 | 16:88698340 | TCACTCCCCACCTGC[A/G]GGCAGCCCCCACAGA | 115992 |
rs76206848 | snp | A/G | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703625 | CCGGGAGTAGTGCCC[A/G]CTTCCCCCACAGGAA | 115992 |
rs76251716 | snp | G/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88707800 | GTGCGTGGTTTTTTT[G/T]TTGTTGTTGTTGTTT | 115992 |
rs76529285 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88702159 | GCTCGCACACCCTCC[C/T]GCTCTGCAGACGCAC | 115992 |
rs76902342 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | CTU2, RNF166 | GRCh38.p7 | 16:88706874 | GCCGTGAAGCTGTCT[C/T]GCCTCCCCGTGTCAG | 115992 |
rs77040866 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | RNF166 | GRCh38.p7 | 16:88703210 | AGGGGGAGAGTCCTG[A/G]GTTTCTTTCTGGAGT | 115992 |