SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9947 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107536 | GGGAACGCATGCAGC[A/G]GGACAGCTCTCCCAA | 57690 |
rs15159 | snp | C/T | 0 | 0 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105066 | GGATGTTCCTCGTAG[C/T]TTTTTATTTTGTGCG | 57690 |
rs1048591 | snp | C/G | 0.245061 | 0.249951 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107603 | AAAACAATGGAAAAT[C/G]TGAGTTCACTCGTGA | 57690 |
rs1079120 | snp | A/C | 0.247053 | 0.249983 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096453 | TTAACATTTATGGGT[A/C]ATCTGCAGGTCTTCA | 57690 |
rs1079121 | snp | A/C | 0.42803 | 0.175514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096264 | ctcccaccctctacc[A/C]tacagcaggccccgg | 57690 |
rs2273280 | snp | A/G | 0.216349 | 0.247725 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107582 | TCACTCGTGAGAGAG[A/G]TACGTATGTGAGCTC | 57690 |
rs2290905 | snp | A/G | 0.426813 | 0.17674 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098030 | AAGCTGATGTGCCCA[A/G]CGTGCCCACTGTGCC | 57690 |
rs2290906 | snp | A/G | 0.361711 | 0.223653 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78097785 | TGGCCAGGCACTCGA[A/G]GAAGGCAGCGTGGCA | 57690 |
rs2290907 | snp | A/G | 0.414905 | 0.187899 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097596 | AGTGACATGTGGGAA[A/G]GAAGAAACGGGGCAT | 57690 |
rs2311001 | snp | C/G | 0.499732 | 0.0115784 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096472 | GCACCAGAGCTGAGG[C/G]AAGTTAACATTTATG | 57690 |
rs2311439 | snp | A/G | 0.185788 | 0.241613 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084005 | TGAGCCACCGTGCCC[A/G]GCCGATTCCTGGTCA | 57690 |
rs2311440 | snp | C/G | 0.179465 | 0.239843 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071204 | GGCATTTCATTTTGG[C/G]AAGCATGGTGGGTAG | 57690 |
rs2311441 | snp | C/T | 0.284471 | 0.247612 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061661 | TCTTGTTACGTTGCC[C/T]GGGCTGAAGTGCAGT | 57690 |
rs2311442 | snp | C/T | 0.203267 | 0.245593 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061273 | TTTGTTAATAATTTA[C/T]AGGGATTCTTTTAAA | 57690 |
rs2311443 | snp | C/G | 0.203267 | 0.245593 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058668 | TATTAGCAGTATACT[C/G]CCTGCCAGTTTTCTG | 57690 |
rs2311444 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051748 | AATCATGCACTGTCA[C/T]TGCTTTCAAATCCAT | 57690 |
rs2871763 | snp | A/G | 0.498253 | 0.0295011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082138 | ATTTCTCGACCTGCC[A/G]ATCTGCCTGGGAACA | 57690 |
rs2871764 | snp | A/G | 0.419616 | 0.183658 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071374 | TTTTTGATAGAAATT[A/G]TGTGGGTCTTTGCTG | 57690 |
rs2871765 | snp | G/T | 0.204803 | 0.245881 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061354 | CACAGAAAATGATTT[G/T]AAGTACATAGAATTA | 57690 |
rs2871766 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056231 | ggtggaagttgcagt[A/G]agacgagattgtgtc | 57690 |
rs3751962 | snp | C/T | 0.185788 | 0.241613 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102638 | CCAAGAACCCCCAAC[C/T]ATCCTGCCCCACCAG | 57690 |
rs3764377 | snp | C/T | 0.186421 | 0.24178 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091673 | AGAATGGCCATGCTA[C/T]ACAACAGGACGATCG | 57690 |
rs3764378 | snp | C/T | 0.00523557 | 0.0508957 | missense | TNRC6C | GRCh38.p7 | 17:78091556 | CACTGGGCAAGTTAT[C/T]CATGGAGTTGGGGTG | 57690 |
rs3764379 | snp | A/G | 0.215144 | 0.247558 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070825 | TATTTCTCTTTCCCA[A/G]ATAATTAATTTAGTT | 57690 |
rs4362447 | snp | C/T | 0.478768 | 0.100824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037481 | AACTAACCCAGACTA[C/T]GGATAGGGGACTGCA | 57690 |
rs4411562 | snp | A/G | 0.283158 | 0.247791 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051531 | ATTCATGAATACTCC[A/G]AGTAGTGTTTTTTAT | 57690 |
rs4564643 | snp | G/T | 0.185155 | 0.241444 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081813 | AGCATGTCCCAAATG[G/T]CAAGGCATCTGTGTG | 57690 |
rs4567792 | snp | C/G | 0.186105 | 0.241697 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082265 | actaagtttagtgag[C/G]gcaggggtaggttag | 57690 |
rs4789012 | snp | A/C | 0.499987 | 0.00259581 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065485 | AAGTCAAAGCAACCC[A/C]GCATATTATGTTTGA | 57690 |
rs4789013 | snp | C/T | 0.340784 | 0.232934 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066347 | GTACTTTGTGGTTTT[C/T]TTTGGTTTTTTTTGT | 57690 |
rs4789523 | snp | C/T | 0.433818 | 0.169443 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016773 | TTATTATACTATAAA[C/T]GCTTACTGTGTACTA | 57690 |
rs4789524 | snp | C/T | 0.127254 | 0.217792 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017306 | ATAGAAGCACCTCAG[C/T]GTGCTCCCACTCCTG | 57690 |
rs4789525 | snp | C/T | 0.372592 | 0.217879 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054695 | TACTGCAGACTACTG[C/T]AGACTACTATACACC | 57690 |
rs4789526 | snp | A/G | 0.375 | 0.216506 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054848 | CATACACCACTGCAG[A/G]CTACTGTACACTACC | 57690 |
rs4789528 | snp | A/T | 0.334182 | 0.235401 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070493 | TCTTCTGTGGTGCCG[A/T]GCCCTCCCCCACCCC | 57690 |
rs4789529 | snp | A/C | 0.343924 | 0.231686 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082207 | GGTCACCGCCTTCTG[A/C]TCCTGTGATGCCACC | 57690 |
rs4789530 | snp | A/G | 0.42574 | 0.177808 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084026 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCATTTT | 57690 |
rs4789531 | snp | A/G | 0.402806 | 0.197864 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085947 | TCACCAACACTAAAC[A/G]GGTATTGACTCTGTG | 57690 |
rs4789532 | snp | C/T | 0.246769 | 0.249979 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092206 | AAATTCAGTAGGTTA[C/T]GTAGTTCTCTCTTGA | 57690 |
rs4789533 | snp | C/G | 0.26326 | 0.249648 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092370 | TTTTTAACATCCACT[C/G]TGTTCTTCCGTAGTG | 57690 |
rs4789534 | snp | A/G | 0.24019 | 0.249807 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101558 | acacagaaatagagc[A/G]gtgtgaagtgggaaa | 57690 |
rs4789535 | snp | C/T | 0.41833 | 0.184838 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101560 | acagaaatagagcgg[C/T]gtgaagtgggaaatc | 57690 |
rs5822227 | in-del | -/A | 0.413748 | 0.188909 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087483 | AGTTTTGCCGCTGCC[-/A]ATAATACTCTCAGTA | 57690 |
rs6502003 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045737 | ATTAGACACTTAATT[C/T]AGGGATCAGATGGGT | 57690 |
rs6502004 | snp | A/G | 0.139225 | 0.224118 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046342 | tgcaccaccacaccc[A/G]gctaatttttgtgta | 57690 |
rs7208011 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082918 | ttcatcttttattcc[A/G]tagcagtagtttcag | 57690 |
rs7208399 | snp | A/T | 0.0085814 | 0.0649389 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083175 | GCAGCTGGTGAGTGG[A/T]TAGACCCATGCAAGT | 57690 |
rs7213081 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046142 | tatccttttcccatt[A/T]ctggttgggttgttg | 57690 |
rs7213788 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012928 | GTTTTTAAAAGTAAG[G/T]GAGAGAATTGGGAAA | 57690 |
rs7221094 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089660 | GAGCAGGCATATAAA[C/T]GGGAAAAAATAACCT | 57690 |
rs7221630 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069595 | gagtctcactttgtG[A/G]CATTTATACAGTTTT | 57690 |
rs7223750 | snp | A/G | 0.00769666 | 0.0615556 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049188 | TGGAGCAGGGGGAGC[A/G]AACAGTAATGGAAGT | 57690 |
rs7225319 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097109 | ggtccctgtgactcc[A/G]gaggctgaggcaaga | 57690 |
rs7225716 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028059 | cgccaccatgcccgg[A/C]taatttttttttgta | 57690 |
rs8068724 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059028 | CCTAAAAAGATGAGA[A/C]GTGTATTGTTTCTAT | 57690 |
rs8069862 | snp | G/T | 0.0836354 | 0.186609 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012332 | actacagacactggg[G/T]tctccttgagggtgg | 57690 |
rs8070508 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046576 | gatatcttttgttat[A/G]tagatgtttttaata | 57690 |
rs8072728 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097208 | gcagcctgggtgaca[C/T]tgcaacagccccatc | 57690 |
rs8073490 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059719 | ctgggcatagtggca[C/G]acgcctctagtcccg | 57690 |
rs8074332 | snp | C/T | 0.49917 | 0.0203505 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004492 | GTGTTTTAAGGAAGC[C/T]GTGTTTTAGTTGCTG | 57690 |
rs8074519 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060000 | TCACATGATGACTCA[A/G]TAAGGCAGGCAGAAG | 57690 |
rs8075795 | snp | C/G | 0.133093 | 0.220981 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095653 | TGTTGCTCCACTCTG[C/G]TACCTCTCTTGGTTG | 57690 |
rs8076133 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056620 | aggtgcccgccacca[C/T]gctcggctaattttt | 57690 |
rs8076215 | snp | A/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006832 | TTTATTTATTTATTT[A/T]TTTTTTTTTTGAGAT | 57690 |
rs8080351 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007200 | ATTTTTCTCTTCTCC[C/T]TCTATATCCTCTAAA | 57690 |
rs8080373 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018584 | TGCATGGGAAAACAA[C/T]GAGTTTGAGCCCTTA | 57690 |
rs8081576 | snp | A/G | 0.205417 | 0.245993 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018954 | ATTCTTGGTGGCAGC[A/G]GGTGCTTATGCTAGT | 57690 |
rs8082514 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103832 | ccgtaatctctcctt[A/G]taaggacaccagtcc | 57690 |
rs9709435 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030883 | gcgagcggatcactt[A/G]aggtcaggagttcga | 57690 |
rs9747433 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034075 | tcttttcttttgaga[C/T]tgagtttctctcttg | 57690 |
rs9889700 | snp | C/T | 0.0263992 | 0.111815 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004071 | CTCCTGTATACCATA[C/T]GCGAAATTCTGACTT | 57690 |
rs9889827 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030590 | atatgagtcagttgt[C/T]gactcaaacgtcatt | 57690 |
rs9890070 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005504 | TATTGATATGTAAAA[A/G]ATTTCTCTTTTTATC | 57690 |
rs9890339 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101874 | ccttccagcatgggc[A/G]tcatggccatcatga | 57690 |
rs9890356 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070626 | TTAATAAAATTAACA[A/G]GTTGTTTCATCCTTT | 57690 |
rs9891107 | snp | A/T | 0.185155 | 0.241444 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024091 | aagagcaaaaaaaac[A/T]ccgtctcaaaaaaaa | 57690 |
rs9891683 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070128 | TCTCCGCTCATGAGG[A/G]GTAGAAGTGATTACA | 57690 |
rs9891875 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063310 | tgtaaggagaaagta[C/T]acttactattcatta | 57690 |
rs9892104 | snp | A/T | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005298 | TGTCTGAAGAATGTT[A/T]TATTAGCTTTCCAAA | 57690 |
rs9893340 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041909 | TTTGTCAGTGTTAGT[A/G]CCAGTACAGCATTCT | 57690 |
rs9893684 | snp | A/G | 0.264632 | 0.249571 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063701 | TGTGGGTGGTACCAT[A/G]GAAACTGTCTGCATT | 57690 |
rs9893685 | snp | A/G | 0.248188 | 0.249993 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063703 | TGGGTGGTACCATAG[A/G]AACTGTCTGCATTTT | 57690 |
rs9893730 | snp | A/T | 0.202035 | 0.245356 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035883 | AAATAAAAGCTCTTA[A/T]CAACTTTCTTAAAAG | 57690 |
rs9894438 | snp | G/T | 0.121384 | 0.214378 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104848 | GGAGTCCCTGTAGGC[G/T]CTGCCATCATCAGCA | 57690 |
rs9895798 | snp | C/T | 0.039522 | 0.134904 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002397 | AGCCAGGACATGTGG[C/T]TCCCGACTGTAACAG | 57690 |
rs9896371 | snp | A/G | 0.499087 | 0.0213463 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002289 | AGAAATGCCCTGAAG[A/G]GTAACAGATTCTTCT | 57690 |
rs9897909 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064230 | cctccccaatagctc[A/G]gattacaagtgcacg | 57690 |
rs9898451 | snp | A/C | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085402 | GCCTATAAGGATTCA[A/C]TTAAGTGGGGTATTT | 57690 |
rs9898929 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041127 | CTGCAGGTATTTCCT[C/T]ACCCGTCAGCCCCTC | 57690 |
rs9899210 | snp | A/T | 0.20511 | 0.245937 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025192 | ttgtgtatctgtcat[A/T]gcagtttccctgccc | 57690 |
rs9899225 | snp | C/G | 0.202651 | 0.245475 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033986 | ACTCTCCGTTTTTCT[C/G]TCTGGCTGTGAAGGC | 57690 |
rs9899282 | snp | A/G | 0.201727 | 0.245295 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040946 | gtggcccggACGCAG[A/G]CTGGCCCCGGGAGCT | 57690 |
rs9899593 | snp | A/C | 0.0558544 | 0.157504 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033796 | CTATGTAGTGAGCAT[A/C]AAATAAGAAATTCAT | 57690 |
rs9899626 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013223 | agatcttctggacca[A/G]agagggagccattgg | 57690 |
rs9899783 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072251 | TTATACTGTCTCAGT[A/T]ATCATGGCACCCTAG | 57690 |
rs9899880 | snp | A/G | 0.421684 | 0.181726 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094143 | TGTGCCACCATACCA[A/G]GCTAATTTTTGTATT | 57690 |
rs9899993 | snp | C/G | 0.204803 | 0.245881 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020639 | aatcattttaaatag[C/G]ctagttgcatcatct | 57690 |
rs9900941 | snp | G/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003035 | ATGGTCAGAATGCGG[G/T]ATAGTGGCATCTAAA | 57690 |
rs9902446 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082027 | TTAAAATGTCCATAC[A/G]TTTTTTAATGGCCTT | 57690 |
rs9904101 | snp | A/C | 0.176861 | 0.239062 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003353 | catccagagaaggaa[A/C]aaagatatgcagaaa | 57690 |
rs9905518 | snp | C/T | 0.103082 | 0.202275 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025366 | ctgtactttcctgat[C/T]ggcttctttcactta | 57690 |
rs9905805 | snp | A/G | 0.143622 | 0.226238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020773 | tctcttttttttggt[A/G]ctaagtctttagaat | 57690 |
rs9906521 | snp | A/G | 0.204803 | 0.245881 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021106 | AGAAAGCTTCCTTCA[A/G]GCAGCACTGTCCAGT | 57690 |
rs9906734 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035585 | tgagggagaaggatc[C/G]cttgagcccaggaat | 57690 |
rs9907233 | snp | A/G | 0.143622 | 0.226238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021384 | TGTGCTCGTTCACTG[A/G]TCCTGTTGTGCTCAT | 57690 |
rs9907255 | snp | C/T | 0.216649 | 0.247765 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035144 | TTCTGACTCAGACAC[C/T]ATTCCAATGACTTTG | 57690 |
rs9907691 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010857 | TAGGTTATTCAAAAG[A/G]GTAAAAATGTATTGC | 57690 |
rs9908840 | snp | C/T | 0.204803 | 0.245881 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022011 | CTATTAGTATCTGGC[C/T]CTTTTCCTGTAGGTC | 57690 |
rs9908896 | snp | A/G | 0.185155 | 0.241444 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023260 | gggtttctggaacca[A/G]tccctcttggatact | 57690 |
rs9909649 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059859 | ctcaaaaaaaaaaaa[A/G]aaaagaaaaagaaaa | 57690 |
rs9909778 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030192 | tctcgctctgtcacc[C/T]agcctggagtgcagt | 57690 |
rs9909805 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081619 | CAGGGATCGGGGGTG[A/G]CTCTGCCATAGCCAC | 57690 |
rs9910024 | snp | C/T | 0.268452 | 0.249318 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030325 | tggcttgtgtgtgtg[C/T]gtgtgtgtgtgtgtg | 57690 |
rs9910230 | snp | A/T | 0.093417 | 0.194889 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021574 | GTTAtttattttttt[A/T]tttttattttcttga | 57690 |
rs9912483 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006836 | tttatttattttttt[A/T]ttttttgagatggag | 57690 |
rs9913902 | snp | C/G | 0.233818 | 0.249476 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095812 | ACTTTGGGTGGCCAA[C/G]GTGGGAGAATCACTT | 57690 |
rs9914539 | snp | C/T | 0.133777 | 0.221342 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035348 | caccttcactccctg[C/T]acttttgactcatct | 57690 |
rs9916037 | snp | C/T | 0.247337 | 0.249986 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060063 | AAGGCCCGTGGTCAG[C/T]TTCTAGAAGGGACCC | 57690 |
rs9916796 | snp | C/T | 0.177182 | 0.23916 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030327 | gcttgtgtgtgtgcg[C/T]gtgtgtgtgtgtgtg | 57690 |
rs10512616 | snp | A/G | 0.133435 | 0.221162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038075 | GCCATATGCAAGACA[A/G]ATATAAGAACTACAG | 57690 |
rs10552029 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006828 | TTTATTTATTTATTT[-/A]TTTTTTTTTTTTTTG | 57690 |
rs10682260 | in-del | -/CTTA | 0.095934 | 0.196885 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012060 | GACTCATCGCTACAG[-/CTTA]GTTGTCTACATGCCT | 57690 |
rs11278223 | in-del | -/ACTCAAAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097293 | CCAGTCAGAAGAAAT[-/ACTCAAAT]TTTTATGGCAAATTT | 57690 |
rs11306576 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039310 | CAATTTCAAATCTTG[-/C]CCCCCCCCCCCCACT | 57690 |
rs11313921 | in-del | -/T | 0.409041 | 0.192888 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093983 | TTTTATTATTATTAC[-/T]TTTTTTTTTTTTTTG | 57690 |
rs11351810 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085843 | TAGGTTGGTTTTTTG[-/T]TTTTTTTTTTTAAGT | 57690 |
rs11432950 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062351 | GCATTTTCTTAGAAT[-/A]AAGAGTATCAAGGGA | 57690 |
rs11470325 | in-del | -/TT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006553 | TTCTTCTTCTTCTTC[-/TT]CTTCTTCCTTCTTCC | 57690 |
rs11651984 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107178 | GAGCATTGAGTTGTA[A/G]AAAAACTGTTGTTTT | 57690 |
rs11867650 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066359 | TTTTTTTGGTTTTTT[C/T]TGTTTTTTGTTTTGC | 57690 |
rs11868296 | snp | A/G | 0.16976 | 0.236773 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020501 | AGTCTTTATGAAAAC[A/G]GGTAATTATTTAGCG | 57690 |
rs11869987 | snp | C/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072433 | TGACTGACATAGTTG[C/G]TGGGACTAGAGAGAG | 57690 |
rs12051678 | snp | A/C | 0.266273 | 0.24947 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083670 | TACATAAATACTATT[A/C]TAGAAGCACAGGAGA | 57690 |
rs12103507 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101328 | tctgagaccgctgca[C/G]cctggactttattgt | 57690 |
rs12150348 | snp | A/G | 0.251296 | 0.249997 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084469 | GAGGTCTGCTTTTCT[A/G]TAAGCAGCAGGGGAG | 57690 |
rs12325933 | snp | C/T | 0.433818 | 0.169443 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076363 | GGTGAGGCTCACGTC[C/T]TCATCCTGCCCCTCG | 57690 |
rs12450518 | snp | A/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003369 | aaagatatgcagaaa[A/T]cttagaagattttca | 57690 |
rs12450754 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086360 | aaaaaaaaaaaaaaa[A/C]CAGTATGTGTCAGCC | 57690 |
rs12601094 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082550 | tgaaactagataact[A/G]tttagaccacaaatt | 57690 |
rs12601189 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029502 | CACCTGTATAGGGCA[C/G]TTAACTATGAATGGA | 57690 |
rs12601622 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053294 | TATAAAGTACTTGGG[A/G]GGATAAGGAGAAGCA | 57690 |
rs12602033 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081417 | GCACTGAGTTGATAG[C/T]GCACAATTATCAATA | 57690 |
rs12952922 | snp | C/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084434 | CTTTGCTGTTTTTTA[C/G]ACACATGTCCAACAA | 57690 |
rs13342749 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045051 | AGCAGGAGAAAGAAT[G/T]ATATGAATGGCCTCA | 57690 |
rs16970738 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004690 | AAATAAAAGCCCTAC[C/T]GTAAACTTCATAGTC | 57690 |
rs16970740 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005399 | AAGAACAACCAAAGG[A/G]TATCTGCATTTTTTT | 57690 |
rs16970741 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014021 | CTTACTAAATGTTGG[A/C]GTAGTTTAACTTTGG | 57690 |
rs16970755 | snp | A/G | 0.438386 | 0.164349 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033947 | TCACAAACCTGCCGT[A/G]GTCACCTAGTTACTA | 57690 |
rs16970757 | snp | A/G | 0.132751 | 0.2208 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037253 | AGCTCTGAGAAGGGA[A/G]GAAGATGCTAGCCTT | 57690 |
rs16970760 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041760 | CTGAAAACCAAGCAG[C/T]GAAGGATTTGTGGTA | 57690 |
rs16970766 | snp | C/G | 0.141596 | 0.225274 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043338 | GCTATAGAGGTGGGA[C/G]AAAAGAGATGGTTGG | 57690 |
rs16970774 | snp | A/G | 0.203882 | 0.245709 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059466 | TCTCAGTGCAAGTCC[A/G]TGGCGTGAGACGTGT | 57690 |
rs16970784 | snp | A/T | 0.387642 | 0.208697 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062601 | ATACAAGCTGTCAAC[A/T]TATCAACAGTGTCAG | 57690 |
rs16970787 | snp | A/G | 0.297382 | 0.245469 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078115 | CCAGTGTTGTTACCA[A/G]TAGTGCCCCTTCCAC | 57690 |
rs16970792 | snp | C/T | 0.413748 | 0.188909 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087937 | CATGGACTAATTTGC[C/T]GTAAGAATTCAGAAG | 57690 |
rs16970795 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088273 | TAGAGCCCTTTGTGT[C/T]GAAGTAGGTAAGACC | 57690 |
rs16970802 | snp | C/T | 0.185788 | 0.241613 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090443 | GGCTCACTGTGCTTA[C/T]GTACCGTGTGGCGTA | 57690 |
rs16970803 | snp | A/G | 0.271972 | 0.249033 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091097 | AATCAAAGACTATTC[A/G]CATTTTCACCTTAAT | 57690 |
rs16970810 | snp | C/T | 0.263809 | 0.249618 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093553 | AGGACAAAACATCTT[C/T]TAAAATTTCGTGAAT | 57690 |
rs16970811 | snp | A/C | 0.231189 | 0.249291 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095099 | GGATGCAGGTTGTAC[A/C]GATCCAAGTCATAAG | 57690 |
rs16970829 | snp | A/G | 0.25634 | 0.24992 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102100 | TCTGTTGTATTAACC[A/G]GAAGAACCTGGGAGC | 57690 |
rs16970840 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108459 | CCTCAGCAAGAGTTC[A/G]TTTTGTGCCTGAGTT | 57690 |
rs17552162 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005696 | TTTCCCAGTGGTTAA[A/G]AGCACCCACTCAGGA | 57690 |
rs17552197 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008393 | CAGGCCAAGTGAGTA[C/T]GTTTGTGTGAAACAC | 57690 |
rs17552589 | snp | G/T | 0.0127068 | 0.0787735 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040780 | GAGGAAGGAAGATCG[G/T]TTTAGTGTCAGCTGC | 57690 |
rs17639398 | snp | A/G | 0.336017 | 0.234736 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033188 | ATGTGATTGGTTGAC[A/G]GTATTGCATCAGTTT | 57690 |
rs17639481 | snp | A/G | 0.115088 | 0.210473 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038006 | AGATGTATACACGGA[A/G]AGTTGCAGATCACTG | 57690 |
rs17639633 | snp | A/G | 0.108048 | 0.20579 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058618 | CTGTGTCTTCCAACA[A/G]TGGCTAGAAGTAAAA | 57690 |
rs28462256 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067673 | CATCATTTGTCCCAC[A/G]ACCCCTAAATTATAT | 57690 |
rs28479003 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045702 | TATTTGCCACGCCCT[C/T]AAGGAACTCACCTTC | 57690 |
rs28485134 | snp | C/T | 0.43555 | 0.167544 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086097 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 57690 |
rs28504407 | snp | A/G | 0.49962 | 0.0137727 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043763 | CTAGCCTCTATCTTC[A/G]TAAGTTCAATTATGT | 57690 |
rs28514992 | snp | A/T | 0.103082 | 0.202275 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026118 | ATCAACTAATTTTTT[A/T]ACATGATGTTGCTGT | 57690 |
rs28538436 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084235 | GTTGCAGTGAGCCTC[A/G]CACCTTTGCACTCCA | 57690 |
rs28540792 | snp | G/T | 0.202035 | 0.245356 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038282 | AATACCAAGTGTTCC[G/T]ACAAATCAAAAGAAA | 57690 |
rs28540926 | snp | A/T | 0.111576 | 0.20818 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070673 | TACTCATTGGAATAA[A/T]CCCCCTCATTTTATC | 57690 |
rs28562067 | snp | A/C | 0.0137139 | 0.0816633 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067761 | TCTGTTTCTAGCTTC[A/C]AAATCTATGCAAGAA | 57690 |
rs28565524 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046014 | ATTGTAGTGTTGTGT[C/G]ACTTTCATCTACAGT | 57690 |
rs28607457 | snp | A/G | 0.357451 | 0.225731 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057079 | TTACCAATTAAAAGA[A/G]ACAAATAAAAAGTTA | 57690 |
rs28612402 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088460 | GCAAGTCTCAAAACT[A/C]CTGGCCTCAAGTGAT | 57690 |
rs28633638 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016856 | CAAGGAACTCTCTCA[A/G]TAAGGGATTCTTAGC | 57690 |
rs28660207 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067343 | AAGACCCTGTTTCAA[A/G]AAAAAGAAAAAAACC | 57690 |
rs28686468 | snp | C/G | 0.130694 | 0.219696 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032775 | TAATTCTAGCATGAC[C/G]TAGAAGTATTTATAG | 57690 |
rs28698915 | snp | G/T | 0.181978 | 0.240568 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018541 | GATATTGACATGTTT[G/T]GGGGGGTGGAGCAAA | 57690 |
rs28715189 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016533 | TAACATTCATCTAGC[A/G]CCTAACACTTTCCAA | 57690 |
rs34051112 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086629 | ATGAGCTATAATTTT[-/C]CCCTGATAGAAGAGA | 57690 |
rs34068829 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031564 | CCCAACCTGCCGGTA[C/T]CAGTACCAGTACTTC | 57690 |
rs34085786 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061409 | AAATTTTCTATTGCA[-/T]TTTCAGTTTTTAGCA | 57690 |
rs34135732 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038333 | GCAAAGAATGTGAAC[-/G]GGGAAGATCATAGAA | 57690 |
rs34136228 | in-del | -/G | | | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78049398 | GCCTGGCCTGTACTT[-/G]GGACATGAAGGAACC | 57690 |
rs34160157 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020655 | CTAGTTGCATCATCT[-/A]AAAAGTAACAGGCGG | 57690 |
rs34218398 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041725 | AAAAGCTGAAGGCTG[-/T]TGTAGCATTTATCCT | 57690 |
rs34238437 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019858 | GGTCTTTTTGAAGAA[-/G]GGGGAATGTCAAGAT | 57690 |
rs34249245 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040115 | TCATAAAATAATACA[-/G]GGGGAAACTAGATTT | 57690 |
rs34286033 | in-del | -/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108573 | GCTTCATGGAGGAGG[-/T]GGCATTTGCCCTGGG | 57690 |
rs34293811 | snp | C/G | 0.193694 | 0.243577 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064785 | ACTCTTGGGGAGAAC[C/G]ATCCTCCCCTTCTAC | 57690 |
rs34358534 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023730 | GGATCACCTGAGCCC[-/G]GGAAAGCCAAGGCTA | 57690 |
rs34407828 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056290 | GCCTCCCAAGTAGCT[-/G]GGGATTACAGGCGAT | 57690 |
rs34416724 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042151 | TTAAGACAGTTACGT[-/G]TGCTTAGATTTTTAT | 57690 |
rs34451927 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058234 | GTTTTACCAGTTAGT[-/G]GGGATGTGGCAGAAA | 57690 |
rs34457245 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072731 | TACAAAAATAATACT[-/A]AATAGTTACATTTTA | 57690 |
rs34462154 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074118 | GCGCTTTACTGCCTT[-/C]CTTGAGCTTAGAAAC | 57690 |
rs34543719 | snp | A/G | 0.0250273 | 0.10903 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086942 | GAAGCAGCCACCACC[A/G]CCACCGCCCCCGCCG | 57690 |
rs34587560 | snp | A/G | 0.0252062 | 0.109397 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051168 | ACCGGTCAAACAGAA[A/G]GACAGCAGTGAAGCA | 57690 |
rs34736610 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039493 | CTAATACTTGCATGC[-/A]AAAATAAGTCCTAGA | 57690 |
rs34746720 | snp | C/T | 0.203575 | 0.245652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066907 | GTGTGACTTAATGCT[C/T]ATAGGTTTGGATCAA | 57690 |
rs34748001 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060517 | TAACTCTGTCGCCCA[-/G]GCTGGAGTGCAGTGG | 57690 |
rs34801511 | in-del | -/G | | | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78049999 | TACTCGCCTGGGGAA[-/G]GGGGCAGTGGCAACA | 57690 |
rs34815077 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059387 | AGGGGTTTGGTAAGT[-/G]GGGGCTGGACTTCAG | 57690 |
rs34833361 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055468 | CACGAGCATCACCAC[-/G]AAACACGTGGGGAAT | 57690 |
rs34853627 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074849 | AGGGCCAGCAGTGGC[-/T]TGGTGTGGCTGCTGC | 57690 |
rs34890474 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036209 | TTCCCAGGTGTCTTA[G/T]TACGTAAACTCTTTG | 57690 |
rs34988207 | snp | A/G | 0.0510106 | 0.151338 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102437 | ACTATCCACTGGCAC[A/G]GGGCCTTGTCAACCA | 57690 |
rs34996511 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040097 | AATGAAACATTGGCC[-/T]TTCTCATAAAATAAT | 57690 |
rs35027602 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068865 | CTCATATATACATGA[-/G]GCTACATGAGACGTG | 57690 |
rs35057293 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027528 | ACTTGTAAAGCAAGG[-/G]AATTGATCCAAGACC | 57690 |
rs35132678 | in-del | -/C | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109110 | AGCCAGGTGCCCAGC[-/C]TTTGTTGTTGTTGTT | 57690 |
rs35293083 | snp | A/T | 0.000283832 | 0.0119095 | missense | TNRC6C | GRCh38.p7 | 17:78086862 | TGCCAGGTTGCGCGC[A/T]CAATCACTAATCTGC | 57690 |
rs35419460 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091759 | TAGTGCATATAAGAT[-/C]CTCAGCTAGTCACTG | 57690 |
rs35435164 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102985 | TGTATTTTTATAACA[-/T]TTTTTTAAAAGAGTC | 57690 |
rs35554570 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012860 | ACCTGAAAGGATTTA[A/G]GTTTGGTCATCTTTT | 57690 |
rs35555105 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005185 | AAAACGAGAATCTAA[-/G]CCTGCCTTTGAAACT | 57690 |
rs35579581 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013999 | CTCCTCCTGCACCAG[-/C]CCTTGTCTTACTAAA | 57690 |
rs35585016 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087407 | TAGGTGTGAGCCACC[-/A]ATGCCCAGCCTCAAG | 57690 |
rs35655650 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004970 | CAATACTAAAAGTTT[-/G]GCTTATAAACTTTCA | 57690 |
rs35711156 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081608 | AGAAGCAGTGCAGGG[-/G]ATCGGGGGTGACTCT | 57690 |
rs35823955 | in-del | -/G | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012832 | TTGTGATTTATCTAT[-/G]CTCACACTTTCTACC | 57690 |
rs35826608 | snp | A/G | 0.0266618 | 0.112339 | missense | TNRC6C | GRCh38.p7 | 17:78079413 | CCGAGTGGCAATCTG[A/G]GTATGTTTGGCAATA | 57690 |
rs35883148 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026502 | AGTTATAATATGCAT[-/G]CCCAGTTTCAGAAAT | 57690 |
rs35887898 | snp | C/G | 0.00121076 | 0.0245747 | missense | TNRC6C | GRCh38.p7 | 17:78093046 | GCCAGTCCTCCCGTA[C/G]CTGTTCCCCATAGCT | 57690 |
rs35906028 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052194 | GGTTCTTTTCTCTCT[-/G]GGGAGTGTGAATACT | 57690 |
rs35923840 | in-del | -/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106769 | ACATACCTTCAAGTA[-/T]TGTTTTAAAAAATAT | 57690 |
rs35939631 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072855 | AATCAAGTCAGTACA[-/T]TTTTCTTATTACAAG | 57690 |
rs36095113 | snp | A/G | 0.0298439 | 0.118454 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083055 | TAAACAGGTTCAAGC[A/G]CAGCTTTTGCAGTTT | 57690 |
rs55704178 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099339 | ACAGATAGTGTATTA[G/T]TCCATTTTCACACTG | 57690 |
rs55756584 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045146 | TGAGCACATTATTGT[A/G]GGTGGGGCAGTAGGG | 57690 |
rs55825837 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069703 | CTTCTACATTATACA[A/G]AACTAAAAGGAAATT | 57690 |
rs56160773 | snp | C/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109220 | CCAAGAAGGCTGTTC[C/T]AATGGGGGAGAAGCC | 57690 |
rs56194158 | snp | A/G | 0.275464 | 0.2487 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081544 | GAGGCCTCAAAAAAC[A/G]GTAGCTTAAACTAGG | 57690 |
rs56196034 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069700 | TCACTTCTACATTAT[A/G]CAGAACTAAAAGGAA | 57690 |
rs56330517 | snp | G/T | 0.20511 | 0.245937 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069766 | AGTACATTGTTAAAT[G/T]AAAAGCAAGGTGCAG | 57690 |
rs56345156 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055200 | AGTATTTTTTATATT[C/T]TTATTCTATGAGCTT | 57690 |
rs56359015 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089067 | CCACCTTCTGGATTC[A/C]AGCAATTCTCCTGCC | 57690 |
rs56696941 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034502 | AGTTCATTGTCCCCC[C/T]GCACCCGTGAGGCTT | 57690 |
rs56716957 | snp | A/G | 0.239326 | 0.249772 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102420 | GAAGTGGGGAGGGCC[A/G]CACTATCCACTGGCA | 57690 |
rs56732267 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006600 | CCTTCTTCCTTCTTC[C/T]TCCTTCTTCCTTCTT | 57690 |
rs56816459 | in-del | -/TTTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100789 | TTTTTTTTTTTTTTT[-/TTTT]GAGATGGAGTTTCAC | 57690 |
rs56886704 | in-del | -/GT/TG | 0.0711004 | 0.174628 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105635 | GTGTGTGTGTGTGTG[-/GT/TG]CATGTGTGGCGCGTG | 57690 |
rs56922305 | snp | A/G | 0.13446 | 0.221699 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099364 | ACACTGCTGATGAAG[A/G]CATACCCGAGACTGG | 57690 |
rs57078929 | in-del | -/TTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006559 | TTCTTCTTCTTCTTC[-/TTC]CTTCTTCCTTCTTCC | 57690 |
rs57112439 | snp | C/T | 0.404384 | 0.196635 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100952 | AGCTAATTTTTGTAT[C/T]TTTAGTAGAGATGGG | 57690 |
rs57222384 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066966 | TCATTTCAGCAGCAC[A/G]TGTACTAAAATTGGA | 57690 |
rs57299219 | snp | A/G | 0.157642 | 0.232314 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012576 | AGCAAATATATGTAT[A/G]TGCAAATGAATGCAA | 57690 |
rs57574050 | snp | A/G | 0.241914 | 0.249869 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095008 | GACCCAGCCCTCCCC[A/G]CTTGTCACACCTGGT | 57690 |
rs57845014 | in-del | -/A | 0.421526 | 0.181876 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106056 | TATAAAGTTAAAGAG[-/A]AAAAAAAAAAAAACT | 57690 |
rs57852968 | snp | C/G | 0.131038 | 0.219882 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074199 | TCACTACAGAAAGCA[C/G]AGAAATACGAAAAGC | 57690 |
rs57876316 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038871 | CTTTACACATATTAA[A/C]TCATTTAATCTTCTC | 57690 |
rs57885030 | in-del | -/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105129 | TTTTTTTTTTTTTTT[-/T]AAGTATAAAAGCTGC | 57690 |
rs57924935 | in-del | -/CA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029836 | ACACACACACACACA[-/CA]TAAGCCAAGGCCTAC | 57690 |
rs57966063 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039192 | GTAGATAGCATTAGT[C/T]TTCCAGTGACCAGCA | 57690 |
rs58189797 | snp | C/T | 0.235273 | 0.249566 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101922 | AGAGAGTTTTTTTTA[C/T]GGCCAGTTTTGGGGC | 57690 |
rs58302380 | in-del | -/CACA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029834 | ACACACACACACACA[-/CACA]TAAGCCAAGGCCTAC | 57690 |
rs58325526 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059859 | TCAAAAAAAAAAAAA[-/G]AAAAGAAAAAGAAAA | 57690 |
rs58348772 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086345 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAA]CAGTATGTGTCAGCC | 57690 |
rs58424290 | in-del | -/A | 0.379746 | 0.213696 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106254 | ATTTAAAAAGGAATT[-/A]AAAAAAAAAAAAGAC | 57690 |
rs58456581 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006576 | CCTTCTTCCTTCTTC[C/T]TTCTTCTTCCTTCTT | 57690 |
rs58601421 | snp | A/G | 0.203575 | 0.245652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066654 | GTGAAAATTTGGGGT[A/G]ATTTTGATACCGAAA | 57690 |
rs58623832 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092215 | AGGTTACGTAGTTCT[C/T]TCTTGATAGGAAGCA | 57690 |
rs58744297 | snp | A/G | 0.278664 | 0.248351 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086317 | CCTGGATGACAGAGC[A/G]AGACTCCATCTAAAA | 57690 |
rs58853616 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067356 | AAAAAAAGAAAAAAA[-/A]CCTACAAATTTTAAA | 57690 |
rs58872473 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085728 | TAGGGAGATAACCAC[A/G]TTGTTTAACACACAT | 57690 |
rs58893422 | snp | G/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108950 | GTTAAGCTCCAGCGA[G/T]CTTCCGACCTCAGCC | 57690 |
rs58953316 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006588 | TTCCTTCTTCTTCCT[C/T]CTTCCTTCTTCCTCC | 57690 |
rs58989432 | in-del | -/TTCTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006556 | TTCTTCTTCTTCTTC[-/TTCTTC]CTTCTTCCTTCTTCC | 57690 |
rs59077074 | in-del | -/G | 0.103794 | 0.20279 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026082 | TTTTTGAGGTCTCTA[-/G]CCTTAGTATTTTTTT | 57690 |
rs59088079 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039075 | CTCTGCATTTGTCCT[C/T]TGCCCAGTGGCATGA | 57690 |
rs59126917 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080169 | GAAAAAAATGTTGCC[A/G]GGCGCGGCGGCTCAC | 57690 |
rs59304499 | in-del | -/TTTTTTTTTTTTTTT | 0.350982 | 0.228698 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088960 | TACACTTATCGTTAC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 57690 |
rs59312538 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034981 | ACGTCTCTGAGCTTT[C/T]TATGACTAAGCAGAA | 57690 |
rs59339483 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006595 | TTCTTCCTTCTTCCT[C/T]CTTCCTCCTTCTTCC | 57690 |
rs59545630 | snp | A/C | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106884 | AAAACAAAAAAAATA[A/C]AAAAAAAAAAAAAAA | 57690 |
rs59705382 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006578 | TTCTTCCTTCTTCCT[C/T]CTTCTTCCTTCTTCC | 57690 |
rs59830345 | snp | C/G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018264 | CCAGAGTAGCTGGGA[C/G/T]TACAGGTGTGCATCA | 57690 |
rs59944470 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006622 | TTCCTTCTTCTTCTT[-/T]CTTCTTCTTCCTTCT | 57690 |
rs59967296 | snp | C/G | 0.0865458 | 0.189163 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012952 | TGGGAAAGGAAAATA[C/G]TGATATGAATGAGGT | 57690 |
rs59983243 | in-del | -/TTCTTCTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006553 | TTCTTCTTCTTCTTC[-/TTCTTCTTC]CTTCTTCCTTCTTCC | 57690 |
rs60028540 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018933 | CATGTTAGGTTAGTA[A/G]GAGGAATTCTTGGTG | 57690 |
rs60074485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017740 | CTGCCTACCTCTCCA[G/T]CCTCCTGTGAAACAA | 57690 |
rs60105040 | snp | A/G | 0.226484 | 0.248892 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102867 | GCCTGGCTGGGCGCA[A/G]TAGCTCATGCCTGTA | 57690 |
rs60249275 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028089 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 57690 |
rs60266017 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089560 | TCAGTAGTGGGGGCT[C/T]CTAGCTACCTTCCTT | 57690 |
rs60286626 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062824 | TTACCAAAAGTATAA[C/T]TTAGGACTTCCCAAA | 57690 |
rs60301901 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006610 | TCTTCCTCCTTCTTC[C/T]TTCTTCTTCTTTCTT | 57690 |
rs60439824 | in-del | -/TT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006627 | TCTTCTTCTTTCTTC[-/TT]CTTCCTTCTTCTTGA | 57690 |
rs60457979 | snp | A/C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106882 | TCAAAACAAAAAAAA[A/C/T]ACAAAAAAAAAAAAA | 57690 |
rs60474749 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085842 | ATAGGTTGGTTTTTT[G/T]TTTTTTTTTTTTAAG | 57690 |
rs60576483 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037139 | CACATTTTGCCATTT[C/T]TTAGACAAACTAGTG | 57690 |
rs60735984 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091327 | AAAAAAAAAAAAAAA[-/A]TTTGCTGTAAGCGAA | 57690 |
rs60783600 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081777 | GAAGAAGCAGTTAGT[C/T]TTCCCCACACAAAGC | 57690 |
rs60867452 | snp | C/T | 0.294832 | 0.245947 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079039 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACTACTG | 57690 |
rs60964524 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030325 | TGTGTGTGTGTGTGT[-/GT]AGTAGAGACAGGGTT | 57690 |
rs60973279 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106537 | TAAAAAAAAAAAAAA[A/C]AAAACAAAACAAAAA | 57690 |
rs60993368 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037966 | GATCCAGGAACTATG[A/G]TATAAAGAGAGCAGG | 57690 |
rs61165309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085841 | AATAGGTTGGTTTTT[G/T]GTTTTTTTTTTTTAA | 57690 |
rs61356080 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048165 | CAGATTTTTTTTTTT[-/T]ATTATGAATGTGCAG | 57690 |
rs61402918 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076233 | AAAAAAAAAGAAAAA[A/G]AAAAAAAAAAAAGGA | 57690 |
rs61463223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037042 | AAATAGTAGATTAAT[C/T]TGACTCTTAAAACAT | 57690 |
rs61558278 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006633 | TCTTTCTTCTTCTTC[-/C]TTCTTCTTGAATTTT | 57690 |
rs61607026 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006612 | TTCCTCCTTCTTCCT[C/T]CTTCTTCTTTCTTCT | 57690 |
rs61730171 | snp | A/C | 0.226481 | 0.248891 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064873 | GGGAGATCACCCTGC[A/C]GAGCCGCCGGTGGCA | 57690 |
rs61742302 | snp | C/T | 0.000614398 | 0.0175163 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083151 | GATGTTGAACCAGCT[C/T]TATCAGCTGCAGCTG | 57690 |
rs62078550 | snp | A/C | 0.444666 | 0.15686 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002692 | GAGGCCAGGAGTTCG[A/C]GACTAGCCTGGACAA | 57690 |
rs62078551 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024815 | CTTTTTTTTTTTTAG[G/T]ACAGAGTCTTGCTCT | 57690 |
rs62078552 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026899 | GGGTGGAGGGCATGT[A/G]GGAGCTATTAATAGA | 57690 |
rs62078554 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030254 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 57690 |
rs62078555 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038489 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 57690 |
rs62078556 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041169 | GAAACGGAACAAACA[C/T]GGAACAAATAGTGGC | 57690 |
rs62078557 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054876 | ACCATACACCACTGC[A/G]GACTACTGTACGCTA | 57690 |
rs62078558 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059133 | TTTAGTATAAAAACT[A/C]CACCAAAAGACAGTC | 57690 |
rs62078559 | snp | A/G | | | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064893 | CGCCGGTGGCATTTG[A/G]AAGAGCTGGCGCACC | 57690 |
rs62079060 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073385 | TGAGAGACACTGGAA[A/C]CACACACTAGACTTC | 57690 |
rs62079061 | snp | A/G | 0.281577 | 0.247998 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084589 | CAGGACCAAGGCTTG[A/G]CCCTCAGAGACTGTT | 57690 |
rs62079062 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093464 | GTTTGTTCCAAAGGA[G/T]TGATTGCTTTAATGA | 57690 |
rs62079063 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106520 | GCACTGAAGATGTTA[A/T]TTAAAAAAAAAAAAA | 57690 |
rs66483463 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070006 | AAAACTTTCTTTATA[C/T]CTTGTTTATACTTTT | 57690 |
rs66560815 | snp | C/G | 0.243633 | 0.249919 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093377 | AGGAAGCACACTGCA[C/G]ACTATCCGGTAAAAC | 57690 |
rs66652880 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010806 | TTTTTCCATGGAAAC[-/A]AAAAAAATATTAAGA | 57690 |
rs66787009 | snp | C/T | 0.289683 | 0.24683 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029328 | GTTGCTACTCACCTA[C/T]GCCATGTGATAGAAC | 57690 |
rs66795527 | snp | A/G | 0.114387 | 0.210022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053877 | TTTCTTTAAACAAAC[A/G]AACAAAAAAGCTCCA | 57690 |
rs66806510 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054667 | CTGCAGACTACTGTA[C/T]GCTACTGGAGACTAC | 57690 |
rs66851133 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030537 | CCAGACGATAGGAAT[C/T]TTTCAATTCCATTAT | 57690 |
rs67026334 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090358 | CACCTGGCTCCTATG[A/G]GCATTTGAATTTGCA | 57690 |
rs67487178 | snp | A/G | 0.100944 | 0.200705 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096623 | TACGGCTGAGATGCC[A/G]TGGCTTTTCAGAAAC | 57690 |
rs67500653 | snp | A/T | 0.0998734 | 0.199905 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062416 | TACATTTTGTAATTG[A/T]TATTGTAATATCCAT | 57690 |
rs67678607 | in-del | -/TTT | 0.0898423 | 0.191962 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042566 | CGGTCATTTCACAGA[-/TTT]TTTTTTTTTTTTTAA | 57690 |
rs67719449 | snp | C/G | 0.274124 | 0.248833 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077645 | CTTCGGCTGCCGGAT[C/G]CATCCAGAGGTCCAG | 57690 |
rs67793638 | snp | C/T | 0.293551 | 0.246177 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054457 | CTGCAGACTACTGTA[C/T]ACTACTGCAGACTAC | 57690 |
rs67825540 | snp | C/T | 0.248188 | 0.249993 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081097 | TGTCTGGTGAGGGCC[C/T]GTTTCTCATAGATGG | 57690 |
rs67866552 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083327 | TTAGGGAGTTCTCAC[C/T]CAAAGGTGTCCTACT | 57690 |
rs71160271 | in-del | -/GAAGAAGAAGAAGAAGAA | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006544 | GGAAGAAGGAAGAAG[-/GAAGAAGAAGAAGAAGAA]GAAGAAGAAGAAGAA | 57690 |
rs71363695 | in-del | -/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073346 | TTTCCCGTTATGTTT[-/T]GAGGGAAGGTAATAA | 57690 |
rs71363696 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108221 | TCAATTCCTTCGAAA[-/A]GATGGGACCCGCACC | 57690 |
rs71385927 | snp | A/G | 0.0325443 | 0.123341 | missense | TNRC6C | GRCh38.p7 | 17:78050542 | TCAGGGGGGAAGAAC[A/G]ATGGGTCCATCATGA | 57690 |
rs71385928 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072378 | TGATGGTGGAGCCTA[A/G]AGTTGATGAAGCGAA | 57690 |
rs71385929 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099484 | CTCACATGGCAGCAG[A/C]CAAGAAGAGAGAGAG | 57690 |
rs72067140 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039318 | ATCTTGCCCCCCCCC[-/G]CCCACTCCCTACCTC | 57690 |
rs72080602 | in-del | -/C | 0.157311 | 0.232183 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017317 | CAGCGTGCTCCCACT[-/C]CCTGCTCTCCTGCTC | 57690 |
rs72217904 | in-del | -/A | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106885 | AAACAAAAAAAATAC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs72225188 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042581 | TTTTTTTTTTTTTTT[-/T]AACGAAATTTAACCT | 57690 |
rs72268824 | in-del | -/CT | 0.0129156 | 0.0793156 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086632 | GAGCTATAATTTTCC[-/CT]GATAGAAGAGACGCT | 57690 |
rs72894037 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009382 | GGTTTTTTTAATGAT[A/T]AACTATGATAATTTT | 57690 |
rs72894039 | snp | A/C | 0.167158 | 0.235875 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011843 | TTCATAATTTTAGCC[A/C]TTCTAATAGGTATGT | 57690 |
rs72894052 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044121 | TATCTATGTTTTCAA[C/T]ATAGATTCATAGTCT | 57690 |
rs72894055 | snp | A/G | 0.167809 | 0.236103 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044501 | CCAGCCAGTCACACG[A/G]TGACTCACACTAGAA | 57690 |
rs72894058 | snp | A/C | 0.0281147 | 0.115184 | missense | TNRC6C | GRCh38.p7 | 17:78050595 | ATCTGGGTGGGTCAA[A/C]GCGCCACCTGCCGCT | 57690 |
rs72894061 | snp | A/G | 0.192401 | 0.243274 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052914 | AAATGTGCCTTTTTG[A/G]CCCACATTTTTTCTG | 57690 |
rs72894064 | snp | C/T | 0.282369 | 0.247896 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054041 | CTCACCTAGGCTATA[C/T]GGTACAGCCTGTTGC | 57690 |
rs72894065 | snp | A/G | 0.210301 | 0.246828 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054195 | TAAAATGGTGCACCT[A/G]TATAGGGCACTTACC | 57690 |
rs72894073 | snp | A/G | 0.208474 | 0.246527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060072 | GGTCAGTTTCTAGAA[A/G]GGACCCCGAATCTGT | 57690 |
rs72894083 | snp | C/G | 0.203575 | 0.245652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067127 | GCAGGAGGACTACTT[C/G]AGCCCAAGAGTTTGA | 57690 |
rs72894085 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068406 | ATAGACACAACTCAT[A/G]TCAACAGAAGTTCTT | 57690 |
rs72894087 | snp | C/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068895 | GTATCTCATTTTTTT[C/G]TAGATGACTGCCCAA | 57690 |
rs72894094 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074878 | GCGGAGAGGATAGAG[A/G]GCGGCAGGGCCAGAT | 57690 |
rs72896206 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094967 | TAAGATGGCAGAGGA[C/G]AGGTGAGGCGCCAGC | 57690 |
rs73373014 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019205 | AATGGGGTTGCAGCC[A/G]GGACTTGAAAAGGCT | 57690 |
rs73373016 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027770 | GACACATCCCAATGT[A/T]AGTGATGGTAACCTG | 57690 |
rs73999610 | snp | C/T | 0.014588 | 0.0841497 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050184 | CAGCCAGAACCCTAC[C/T]GTACAGCCTGGTGGT | 57690 |
rs73999613 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061618 | AGTTCGAGGCTGCAG[C/T]GCACTATGATCACAC | 57690 |
rs73999621 | snp | C/G | 0.163564 | 0.234582 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069041 | GACCAAAATCTAAAA[C/G]CCATAAAATAAAATT | 57690 |
rs73999625 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074637 | TATCCCCCACATCTG[G/T]AAGAATACTTGCAGA | 57690 |
rs73999626 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074638 | ATCCCCCACATCTGG[A/T]AGAATACTTGCAGAT | 57690 |
rs73999627 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079763 | GCTTGCTCCTTGGAA[C/T]GCCTCAGCCACCGAA | 57690 |
rs73999628 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081272 | TTTCAACATAGGAAT[G/T]CTCGGGGGACGCAGA | 57690 |
rs74255301 | snp | A/T | 0.198014 | 0.244535 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053978 | ATTTCAGCATTGTGT[A/T]AACATTATAAAGTAT | 57690 |
rs74256103 | snp | A/G | 0.185472 | 0.241529 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073692 | CAGGGTTGGGTTCCT[A/G]TGAGCCTCTGCTCAC | 57690 |
rs74321817 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022969 | ATTACATTAGGTATT[A/G]TAAGTAATCTAGAGA | 57690 |
rs74333062 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075742 | GCATCTGTGGAAAAC[A/G]CCCTGAATGTTTAGC | 57690 |
rs74360347 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004673 | CTATTAGTAAAGATT[A/T]AAAATAAAAGCCCTA | 57690 |
rs74525067 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055830 | GGCCTCATTTTACAA[A/C]TGAGACCTAGGAGAT | 57690 |
rs74548385 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014893 | CACAGCAGATGGACC[C/G]TCCGTACTCAGAGCT | 57690 |
rs74602215 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005880 | AATGTAAAAAAAAAA[A/G]ACTAATTGAGATCAT | 57690 |
rs74603808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041810 | GTATACTATCAACTG[C/T]TGAAAGCATTGCGAA | 57690 |
rs74655233 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075631 | GAAATTACGTGTTAG[A/G]TGTTTATCCTCAGGA | 57690 |
rs74665885 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062103 | TTATTAGCTATGTTA[A/T]CGTCTCTGATTTAAT | 57690 |
rs74667773 | snp | C/T | 0.138207 | 0.223612 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044446 | TAGAGCCAGAATAGG[C/T]ACGCCTTGCCTTCAT | 57690 |
rs74677655 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058640 | GAAGTAAAATATCAT[C/T]ACATATGCCAATCAG | 57690 |
rs74751636 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063460 | TTTGTATAAATGGAT[C/T]ACTGAAGTTCACACC | 57690 |
rs74757807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022138 | ATATATTTGTCTTTG[A/G]GTTTTTCCCCCATCC | 57690 |
rs74804537 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025237 | GCTCCGCATAGTCAT[C/G]CCCCACTCCCCTGGC | 57690 |
rs74894602 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093492 | TGAAAGAGAGTATAA[A/G]GTGTACCTCTAATTT | 57690 |
rs74934233 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057203 | TTTCATTTATAACAT[A/T]AATCTCTTTTTCTAC | 57690 |
rs75041193 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015218 | CTATGCTTTATCTTA[C/T]AAAAGCTTGTTTCTT | 57690 |
rs75086730 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077726 | TGATCTGCGAGAAAG[C/G]ACCACATTCTCCCCC | 57690 |
rs75161016 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106535 | TTTAAAAAAAAAAAA[A/C]ACAAAACAAAACAAA | 57690 |
rs75175955 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108562 | GGATGTGGCAGGCTT[C/G]ATGGAGGAGGTGGCA | 57690 |
rs75227590 | snp | A/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024812 | ATACTTTTTTTTTTT[A/T]AGGACAGAGTCTTGC | 57690 |
rs75273944 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065889 | TTTTGCAATGTGATA[C/T]TTGTAATATTAACAT | 57690 |
rs75330340 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101176 | CTTGGAAATTTCTTC[C/T]GCCAGATACCCTAAA | 57690 |
rs75331168 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087507 | CTCAGTATAAAACCT[C/T]TAAAGGTAGTACCAG | 57690 |
rs75350359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082814 | GGGGGAAGCACATCA[C/T]GCGCTGTTGGCTCAT | 57690 |
rs75382693 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105762 | TATACGCTTTTTTTT[G/T]GGCGCATTGGTCAAA | 57690 |
rs75394492 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087097 | CTTACCCTCTCGGTG[A/T]GTGTCCCATGGTCTT | 57690 |
rs75465097 | snp | A/G | 0.203575 | 0.245652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090879 | GAACTGAATTATCCT[A/G]TCAGTCTGTTTCATA | 57690 |
rs75507142 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028633 | TCCATGTTGAGAGAC[A/C]AAAACTGCAGGTAGA | 57690 |
rs75516895 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018438 | CCAGCCGGAACCATG[G/T]TTTTTTATATAATAC | 57690 |
rs75588831 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082123 | ACGGGGCTCTTTCTT[C/T]GTTCCCAGGCAGATC | 57690 |
rs75702970 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071424 | TAGAATAGAAAATGC[C/T]TTTTTTTTTTGGAGA | 57690 |
rs75740987 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098929 | GGATCTGGATTTCTG[C/T]TTTTTATATTTGCTT | 57690 |
rs75751897 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057608 | TTTCCATAGCTACTG[C/G]GATTCCCAGACAAAA | 57690 |
rs75792047 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027614 | CCCAGGACACGCAAA[G/T]TCCCTAAGATAGGAT | 57690 |
rs75821710 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106901 | AAAAAAAAAAAAAAA[A/G]TCCTGCAAGACTGCA | 57690 |
rs75986775 | snp | C/T | 0.127599 | 0.217986 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012404 | GCACTGGGTTTCATA[C/T]CTGGGTGATGAAATA | 57690 |
rs76043408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022278 | AAAATGAGTCTGTCT[G/T]AGATATAAGATTGAC | 57690 |
rs76103330 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067436 | TTTCATACCATGTAG[A/C]GATTGCCACCTTCCC | 57690 |
rs76122964 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093955 | GGAAATCAATTTGAG[C/T]TTCTGCTGGATTTTT | 57690 |
rs76171073 | snp | C/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108292 | GTGTGCTGCTGGCTC[C/T]GACCATACTCTTTTG | 57690 |
rs76175713 | snp | G/T | 0.095934 | 0.196885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016632 | TCCTGAGTACAGCTG[G/T]CATTACCTCTTCTAA | 57690 |
rs76179842 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035143 | TTTCTGACTCAGACA[C/G]CATTCCAATGACTTT | 57690 |
rs76190778 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068233 | CTCTTAAGCCAGACA[A/T]AGAGATTTGCCAAAA | 57690 |
rs76297082 | snp | A/T | 0.077417 | 0.180873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029623 | AACTTACTTAAAAAA[A/T]TTTTTTTTCAGTAAT | 57690 |
rs76300649 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035083 | TTTCTCATCTAAAAT[G/T]AGAGGTTTGAACCTC | 57690 |
rs76311281 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040316 | CAGCTTGAAACACTT[C/G]AGAGCTTTTATCTTT | 57690 |
rs76394986 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095407 | TGGCCTTTGAGATAA[A/G]GCAAGGAAATGGCAT | 57690 |
rs76402227 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014040 | GTTTAACTTTGGCTC[C/T]CTCTTCTGGCGGGTT | 57690 |
rs76493839 | snp | G/T | | | missense | TNRC6C | GRCh38.p7 | 17:78049697 | ACTGGGGCATGGCTG[G/T]TGGTATGGGGGCCAT | 57690 |
rs76501278 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073335 | TTTTCTCATATTTTC[C/G]CGTTATGTTTTGAGG | 57690 |
rs76523536 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009915 | GAGAGAGAGGGTCTA[A/T]CTCTGTTGCCCAGGC | 57690 |
rs76557606 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103363 | TTTGGAAGGCTGTAG[A/T]GAAAGAAATCAGAAG | 57690 |
rs76565076 | snp | A/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083815 | TTCACATAATCTTGA[A/T]TTTTTTTTAATTTTC | 57690 |
rs76650272 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088661 | CTGGAGTGCAGTGGC[A/G]TGATCATAGCTCATT | 57690 |
rs76717748 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083823 | ATCTTGATTTTTTTT[A/T]AATTTTCAATCAGTC | 57690 |
rs76780965 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019769 | CCTGTATTCTCCTGC[C/T]GCATGAAAATGCTGA | 57690 |
rs76788315 | snp | C/T | 0.143284 | 0.226079 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048465 | TTTTATTCAAAACTC[C/T]ACGTGAACTTACTGT | 57690 |
rs76803261 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062836 | TAACTTAGGACTTCC[C/G]AAAAACTTAACTACT | 57690 |
rs76811565 | in-del | -/GA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063663 | TGCCTTCTAAGACAG[-/GA]ATACCTCAGATCTCT | 57690 |
rs76819046 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019330 | AAAAGTCTGAAAAGG[A/C]GCTCTTTCAAAATCA | 57690 |
rs76903877 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014281 | ACAAGCTCTACACCC[A/G]GTGGACTTTCTTTGC | 57690 |
rs76911859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037216 | AGAATGTTCAGGCAG[C/T]AGTGCCACACTCGGC | 57690 |
rs76975055 | snp | A/G | 0.108402 | 0.206034 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043533 | CACATCAGGATAAAT[A/G]GGGTATCAGTCATCT | 57690 |
rs76990579 | snp | C/T | 0.153 | 0.230415 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006620 | TCTTCCTTCTTCTTC[C/T]TTCTTCTTCTTCCTT | 57690 |
rs76992006 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027607 | TTGAAGACCCAGGAC[A/C]CGCAAAGTCCCTAAG | 57690 |
rs77047304 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084282 | AAGACTCCGTCTCAA[A/G]AAAAAAAAAAAAGAA | 57690 |
rs77089997 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066326 | AAATGCAACTTTATT[A/G]GTTTTGTACTTTGTG | 57690 |
rs77095378 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098999 | CCAAAACAAAACAAA[C/T]CCCACCAGTTTGAAA | 57690 |
rs77100631 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006774 | ACTTTACGCAGAGCT[A/G]TCATTTTCTATTACT | 57690 |
rs77182055 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039310 | CAATTTCAAATCTTG[C/G]CCCCCCCCCCCACTC | 57690 |
rs77187687 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004669 | AATCCTATTAGTAAA[A/G]ATTAAAAATAAAAGC | 57690 |
rs77194075 | in-del | -/AACA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086359 | AAAAAAAAAAAAAAA[-/AACA]GTATGTGTCAGCCAC | 57690 |
rs77245599 | snp | C/T | 0.113334 | 0.209338 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073336 | TTTCTCATATTTTCC[C/T]GTTATGTTTTGAGGG | 57690 |
rs77255486 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078156 | CCGACTGTGTGATCC[C/T]GGCGATCTGACATTG | 57690 |
rs77267104 | snp | A/C | 0.444444 | 0.157135 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100525 | TCACAACTGGAGCGG[A/C]TGGGACACAAGGCAC | 57690 |
rs77307352 | snp | C/G | 0.136847 | 0.222927 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044449 | AGCCAGAATAGGTAC[C/G]CCTTGCCTTCATGGT | 57690 |
rs77337660 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058934 | TAAAACCAGAGGTTG[G/T]GTGCATTAATCATGG | 57690 |
rs77370231 | snp | A/T | 0.0792508 | 0.182605 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012507 | AATAAAGGCTTTTTT[A/T]AAAAAGTTCCCTGTT | 57690 |
rs77376829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062958 | CATTATTAAGAAAAT[C/T]GTAAAGACTGGGTAC | 57690 |
rs77446389 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026698 | TTTTATTCTGAGAGC[A/G]TTACAAGACCTCAGA | 57690 |
rs77476819 | snp | C/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039418 | TGGGCAGAAGCTTCA[C/T]TGGTTTTGTAGCGTT | 57690 |
rs77516693 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058126 | ACATTGCCTCAATTA[C/G]TCAGTCTCTGGTGCG | 57690 |
rs77591363 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029088 | TGCAACTTACTCTAA[A/T]ATGATTTTAGACCTT | 57690 |
rs77675894 | in-del | -/TG | 0.237593 | 0.249692 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108493 | ACTACAGGGGCAAAC[-/TG]TACCCGTGCCTGTGC | 57690 |
rs77711618 | snp | G/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084636 | CTTTTTTTTTTTTTT[G/T]TGAGACGGCGTCTTG | 57690 |
rs77832597 | snp | A/C | 0.185472 | 0.241529 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087530 | AGTACCAGTCAGAGC[A/C]CCCAAAATCTCATTT | 57690 |
rs77846130 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094456 | TTTTTTTTTTTTTTT[G/T]GAGACAGATTCTCGC | 57690 |
rs77850162 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102766 | CATGTTCCTGGTGAA[C/T]TGTTTGTTTCCCCAC | 57690 |
rs77853426 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031972 | AGACAGACAAATTCA[C/T]TTCATTTTAAGTGGG | 57690 |
rs77879497 | snp | A/G | 0.00969282 | 0.0689381 | missense | TNRC6C | GRCh38.p7 | 17:78050645 | GGGGAGACAGCAACA[A/G]CAAAGCGCCAAGTGG | 57690 |
rs77900905 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094457 | TTTTTTTTTTTTTTT[G/T]AGACAGATTCTCGCT | 57690 |
rs77923355 | snp | A/G | 0.188631 | 0.242351 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088003 | TATTAGAGTCTGTAG[A/G]TACAGGACAAAGGGT | 57690 |
rs77977687 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084325 | GAATCATGAAGGAGA[A/G]AAAAAAAAAAAAAAG | 57690 |
rs78027746 | in-del | -/TTT | | | splice-acceptor-variant | TNRC6C | GRCh38.p7 | 17:78005055 | TCTTTTTTTTTTTTC[-/TTT]AGGCTGCTGATCAAA | 57690 |
rs78045209 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090589 | CCTGCTCCAAACTAG[C/T]GTCCTCATCAGAAAC | 57690 |
rs78059684 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015605 | ATGTTGTCTAGGTAG[A/T]TGGAAGATTTAAATG | 57690 |
rs78124491 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106883 | CAAAACAAAAAAAAT[A/C]CAAAAAAAAAAAAAA | 57690 |
rs78173077 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031117 | CACTTAAAAAAAAAA[A/G]GAAAGAAAGAAATGC | 57690 |
rs78313950 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, missense | TNRC6C | GRCh38.p7 | 17:78004178 | TTAATAGGGAGAAAG[A/C]GCAAGAAACACAAGA | 57690 |
rs78331724 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066228 | AGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 57690 |
rs78381256 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061717 | AAATGGAAATATTTG[G/T]TTTTTTAATTTTTTT | 57690 |
rs78386337 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026364 | GAGGTGACATTTAGT[C/T]TGATATTTAAAGAAT | 57690 |
rs78429252 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056798 | TGTTTTTAGTAGCCA[A/G]AACATGGGAGCTTCA | 57690 |
rs78503410 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028289 | GGGAACAAGGAGGTA[A/G]AGGGATTAGGAGCTC | 57690 |
rs78542065 | snp | C/T | 0.184203 | 0.241186 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090264 | GGTTGGCCCCAGTAG[C/T]ACCTGTTTATTTAGA | 57690 |
rs78682911 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011601 | GTTCATGGACATCTG[C/T]GTTTTTCCAGTTTTG | 57690 |
rs78684306 | in-del | -/G | 0.277067 | 0.24853 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077098 | TATTTATCCATCCAC[-/G]GCCTCCTCTGTTTCC | 57690 |
rs78729219 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065359 | ATCTCTTTAAAAAGG[A/G]AAAAAAAAAAGCCAA | 57690 |
rs78731097 | snp | C/G | 0.185472 | 0.241529 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087798 | TTGTAGAAGCACACT[C/G]AGCACTTGAAACCCG | 57690 |
rs78752777 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105779 | GCGCATTGGTCAAAC[A/G]GTTGTTATTATTAGC | 57690 |
rs78797731 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021433 | AGTAAAAGCACCTGC[A/G]TTTCTAAGAGAGTGA | 57690 |
rs78816882 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084338 | GAAAAAAAAAAAAAA[A/G]AGAATGGGAACTCCA | 57690 |
rs78820836 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037154 | CTTAGACAAACTAGT[A/G]TACTGGCTTCACACT | 57690 |
rs78912300 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075624 | CCCTTTGGAAATTAC[A/G]TGTTAGATGTTTATC | 57690 |
rs78918934 | snp | A/G | 0.00521798 | 0.050811 | missense | TNRC6C | GRCh38.p7 | 17:78049796 | GTGCTGAAGGAATAA[A/G]CAATTCTGTGTGGGG | 57690 |
rs79018681 | snp | C/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077607 | TTGGGACTGGCTAAA[C/G]TGATGATGTGTTGCA | 57690 |
rs79160285 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086406 | AAGAGTGGCTAGGTT[A/C]TCTTTTTTTATTTTT | 57690 |
rs79244203 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003485 | ACAATTTTAAACATC[A/T]CAATAAAAAACTCAG | 57690 |
rs79247944 | snp | A/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068888 | GAGACGTGTATCTCA[A/T]TTTTTTCTAGATGAC | 57690 |
rs79266978 | snp | C/T | 0.134119 | 0.221521 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036156 | GAGCAAAGTGAAGCT[C/T]GGAGTTCTTTCAGCT | 57690 |
rs79268643 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107778 | GCAGCAAGAAGATGC[C/T]GGGGCTTGCCTGGAG | 57690 |
rs79324348 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004670 | ATCCTATTAGTAAAG[A/G]TTAAAAATAAAAGCC | 57690 |
rs79336904 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043858 | TTAATTAACATAGTG[A/C]CCTCCAGTTCCATCC | 57690 |
rs79338146 | snp | A/G | 0.136847 | 0.222927 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044175 | AAAAGATTTTGAGCT[A/G]TCAGTTCCTCTTGTA | 57690 |
rs79364228 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092551 | AATTGTTCTTCAAGG[A/G]TTTCAATCTTTCAGG | 57690 |
rs79390211 | snp | A/T | 0.131038 | 0.219882 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031297 | TTTACAGATGAGGAA[A/T]CCAAGGCCCAGGAAT | 57690 |
rs79407794 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096180 | GAGAACAGACAGCTC[A/G]CACGTTCCCACTTAC | 57690 |
rs79494447 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036236 | TTTGTGCCCTCCCCC[C/T]AGGTTTTAGTGTGCT | 57690 |
rs79538619 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074644 | CACATCTGGAAGAAT[A/C]CTTGCAGATACAGGA | 57690 |
rs79584551 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025573 | GGTTTTTGTATGAAC[A/G]TAAAGTTTTCAACTC | 57690 |
rs79593141 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024813 | TACTTTTTTTTTTTT[A/G]GGACAGAGTCTTGCT | 57690 |
rs79638267 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076678 | AAAAGACCTGGCACA[C/T]AGCATGACCTCAGTA | 57690 |
rs79662214 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042824 | GTGTTGGTGATGGTC[A/G]TAACAGTGGTGATGG | 57690 |
rs79709129 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074025 | CCATATCATTGATTC[A/C]TGATCATTGAACTCA | 57690 |
rs79737691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063893 | TCATTACATATAATA[A/C]AAGATGTAAACAAGC | 57690 |
rs79742338 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043859 | TAATTAACATAGTGA[C/T]CTCCAGTTCCATCCA | 57690 |
rs79748351 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044384 | AATGTATGTTTATTT[A/G]CTGCTTCTTCTCTGT | 57690 |
rs79810498 | snp | C/G/T | 0.0236838 | 0.106277 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058023 | AACAACAGTATTAGT[C/G/T]CAGAGAAATATCCCT | 57690 |
rs79816654 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036098 | CAGGGGGCCGCTGAG[G/T]GAGGCGTCCTTAGGA | 57690 |
rs79873588 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044107 | TTATTATCAAACCCT[A/G]TCTATGTTTTCAACA | 57690 |
rs79919552 | snp | A/C | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083608 | AGAACCACAGAACAC[A/C]AAAAATCATTTGAGT | 57690 |
rs79964326 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043855 | TAGAACTGGAGATCA[C/T]TATGTTAACTAAAAT | 57690 |
rs79999986 | snp | C/G | 0.040671 | 0.13668 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041689 | GTAAATGCAGTAGAG[C/G]GGGAGGCATCTTTGG | 57690 |
rs80062865 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031986 | ATTTCATTTTAAGTG[A/G]GTTTTAAAATTTAAT | 57690 |
rs80095363 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023156 | AATTAACAACATAAC[A/G]TATGCGGGAGGATAT | 57690 |
rs80111237 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069365 | ACCTGCCATTTTTCA[G/T]CTCTCAGACCCACAG | 57690 |
rs80168456 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042361 | CATTCCTTACTGTTT[A/G]TTAGTTACAAACCCT | 57690 |
rs80261573 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016769 | AGGATTATTATACTA[C/T]AAACGCTTACTGTGT | 57690 |
rs80285295 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006632 | TTCTTTCTTCTTCTT[C/T]CTTCTTCTTGAATTT | 57690 |
rs80291242 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084283 | AGACTCCGTCTCAAG[A/G]AAAAAAAAAAAGAAA | 57690 |
rs80293256 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069368 | TGCCATTTTTCATCT[A/C]TCAGACCCACAGAAA | 57690 |
rs111254475 | in-del | -/TT | 0.0898077 | 0.191933 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015414 | CCCTCCCAGTTAGCA[-/TT]TTTACCTATAAAAAG | 57690 |
rs111255480 | snp | A/G | 0.176219 | 0.238865 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036704 | CGAGGCAGGTGGATC[A/G]CCTGAGGTCAGGAGT | 57690 |
rs111275118 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073393 | ACTGGAACCACACAC[C/T]AGACTTCAGTGGACA | 57690 |
rs111284759 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076238 | AAAAGAAAAAGAAAA[A/G]AAAAAAAGGAAAGGC | 57690 |
rs111289800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086666 | TTGATGAACTATTAG[A/G]TGATCATTGATTTTT | 57690 |
rs111290258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088596 | ATTAAATGAGCTAAT[A/G]TGTAAAGTTCTCTTT | 57690 |
rs111290905 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036832 | GGGAGGCTGAGGCAA[A/G]AGAATCACTTGAATC | 57690 |
rs111383871 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037821 | ATAGACTAATTCCAA[A/G]CTTCATCTAGAAGAG | 57690 |
rs111431351 | snp | A/G | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066075 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCTGGA | 57690 |
rs111456579 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071548 | GTGAGCCACCATGCT[C/T]GGCTAATTTTTGTAT | 57690 |
rs111485330 | in-del | -/A | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069210 | GATTTAAAAAAAAAA[-/A]TCAGCCAGAAACCCA | 57690 |
rs111530197 | snp | A/G | 5.06898e-05 | 0.00503412 | missense | TNRC6C | GRCh38.p7 | 17:78049192 | GCAGGGGGAGCGAAC[A/G]GTAATGGAAGTGCGG | 57690 |
rs111532609 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029385 | ACAGCATGTTACTAT[A/G]CTGAATACTGTAGGC | 57690 |
rs111587793 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060189 | TCTGACTGTACTCTT[A/G]TATAATGAGCAAACT | 57690 |
rs111614441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066507 | CATTTTGAGCATTCT[A/G]TTTTGAGAATTTGTC | 57690 |
rs111693954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089449 | GTTGTAAAATTGCCT[A/G]TCTTGTTGGCTCTCA | 57690 |
rs111702015 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034035 | CCCAACATTTTCCCC[A/G]CCTACTCTCCATGGC | 57690 |
rs111703086 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093829 | TTTGGAGATGTCAGG[G/T]GTGACAGGTTGGGCT | 57690 |
rs111712070 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037447 | CAGAGATAAGCATAG[A/G]GTGCCACATGGGAAG | 57690 |
rs111715861 | snp | G/T | 0.113334 | 0.209338 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036581 | AAGAATAGATAAAAT[G/T]TATATTTATATACTG | 57690 |
rs111722503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072185 | TTGGTGGCCCAGGCT[C/T]TGCCTGTGTGAGTGG | 57690 |
rs111733705 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009594 | AGTTTTGCTCTTGTT[G/T]CCCAGGCTGGAATGC | 57690 |
rs111770573 | snp | A/G | 0.132751 | 0.2208 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038501 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 57690 |
rs111772460 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051815 | AAGATAGGATAGACA[C/T]GGTTCAGAACTTGGG | 57690 |
rs111778364 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078991 | CCAGCTCCTCGGGAG[A/G]CTGAGACAGAGAATT | 57690 |
rs111794537 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036741 | CCAGCCTGGCCAACA[C/T]AGCGAAACCCCATCT | 57690 |
rs111808078 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057139 | TCACATGCTGAAAGT[A/G]TGTTAAGTTTAGTAT | 57690 |
rs111825956 | in-del | -/G | 0.0858192 | 0.188533 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037513 | GGAAGCCTTTCTGGT[-/G]GAGGTGATATGAGCT | 57690 |
rs111853255 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104904 | CCCCTCCCGGCTGGG[C/T]GGCCCCACAGACCCG | 57690 |
rs111914647 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053852 | GCCTGGGCAACATAA[C/T]GAGACCCCATTTCTT | 57690 |
rs111963459 | in-del | -/A | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013119 | CAAGCTATTCTACCC[-/A]AAAAAAGAGTTGAAA | 57690 |
rs111965938 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018419 | TAGGCGTGAGCCACC[A/G]TGCCCAGCCGGAACC | 57690 |
rs112045578 | in-del | -/TTG | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085780 | GTTACTACCAGTGTT[-/TTG]TCACATTGTCTGGGC | 57690 |
rs112060942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073690 | TACAGGGTTGGGTTC[C/T]TATGAGCCTCTGCTC | 57690 |
rs112103364 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021997 | AAGTAGTTGGAACTC[-/TA]TTAGTATCTGGCTCT | 57690 |
rs112124071 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092741 | GTTGTCTCAAAAAAA[A/T]AAATAAATAAATAAA | 57690 |
rs112133641 | snp | G/T | 0.0186254 | 0.0949353 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060055 | TGCAGCTCAAGGCCC[G/T]TGGTCAGTTTCTAGA | 57690 |
rs112260153 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030292 | ATAGCTGGGATTACC[C/T]GTACCTGCCACCACA | 57690 |
rs112279091 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028591 | GGTAGTGTGGACAAT[A/G]TAGCGTTCACATGGT | 57690 |
rs112281690 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016173 | GGCTCTCTTGACTTC[C/T]AGAGCACAGTGCCAC | 57690 |
rs112283214 | in-del | -/TT | 0.0345262 | 0.126772 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045551 | CAAAGCAGTCTGGGC[-/TT]TGTACAAGTGCAGCT | 57690 |
rs112285195 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048486 | AACTTACTGTCATTG[C/T]CAGTGTTTCTCAGTC | 57690 |
rs112286052 | in-del | -/ACAC | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029809 | TTATTAAAAACCTAG[-/ACAC]ACACACACACACACA | 57690 |
rs112323203 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101559 | CACAGAAATAGAGCG[A/G]TGTGAAGTGGGAAAT | 57690 |
rs112331029 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054293 | AAGGCTTGGGACACT[A/G]CTGCACACTACTGCA | 57690 |
rs112335364 | snp | A/G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053356 | AAGATTAGGTCGGGC[A/G/T]TGGTGGCTCATGCCT | 57690 |
rs112340144 | snp | G/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085965 | TATTGACTCTGTGAT[G/T]TTTTTTAGTTCTGCG | 57690 |
rs112359480 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002715 | CTGGACAACATAGCA[C/T]GCCATCTCTGTTTAC | 57690 |
rs112398196 | in-del | -/A | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066227 | CAGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs112414610 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073148 | TGTGAAGTTTTACTT[G/T]CCAGAAGCATTTGAT | 57690 |
rs112421609 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077107 | CATCCACGCCTCCTC[C/T]GTTTCCTTGGGAAAC | 57690 |
rs112423511 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054917 | CTGCGGACTACTGTA[C/T]GCTACCATACACCAC | 57690 |
rs112449282 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028662 | GACTGGAGCTGACAA[C/T]GTAAAGGGAAACAGT | 57690 |
rs112495997 | snp | C/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046953 | TTTTACAGTGTGACT[C/G]TTGTGGAATGGAACC | 57690 |
rs112516109 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015583 | CTAGCTCATACCACA[C/T]ACTGTGATGTTGTCT | 57690 |
rs112524098 | in-del | -/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069942 | AACTGCTATGAGTAG[-/T]TGCCTCTTCGAGAGA | 57690 |
rs112644354 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069416 | TTTATTTAAAAAAAT[A/T]TTTTTAGAGACAGAG | 57690 |
rs112670845 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075477 | ATGTTACTGAGAATG[A/G]AAAAGACTGGGATTG | 57690 |
rs112729090 | in-del | -/G | 0.430285 | 0.173197 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076238 | AAAGAAAAAGAAAAA[-/G]AAAAAAAGGAAAGGC | 57690 |
rs112753519 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019959 | GACAAAAAAAGAAAA[C/T]GCCCATTTAATTTAT | 57690 |
rs112800878 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020723 | ATATCGCCATTTCAA[C/T]GTGAAAGCAACAGAA | 57690 |
rs112817053 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108718 | TGTCCAGGGCACCAT[G/T]TCCACCCATGGGTGA | 57690 |
rs112838966 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053352 | AAATAAGATTAGGTC[A/G]GGCGTGGTGGCTCAT | 57690 |
rs112920318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080360 | CTGAGGCAGGAGAAT[C/T]GCTTGACCCGGGGAG | 57690 |
rs112924722 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074781 | AGGAAGCAAGTCTTG[A/C/T]AGAAAACTAGGGGAG | 57690 |
rs112927668 | snp | C/T | 0.00278809 | 0.0372327 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067785 | GCAAGAAGGCTGGGG[C/T]AGTGGTGGGGATGAA | 57690 |
rs112953356 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023731 | GGATCACCTGAGCCC[A/G]GAAAGCCAAGGCTAC | 57690 |
rs112963049 | in-del | -/GT | 0.5 | 0 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105634 | CGTGTTGAAACAGAA[-/GT]GTGTGTGTGTGTGTG | 57690 |
rs112981222 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054803 | ACTACTGTACACTAC[C/G/T]ATACACCACTGCAGA | 57690 |
rs113008916 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034144 | CCACAACCTCTGCCT[A/C]CCAGGTTCAAGTGAT | 57690 |
rs113064593 | snp | C/T | 0.20511 | 0.245937 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091280 | GCAATGAGCCAAGAT[C/T]GTGCCATTGCACTCC | 57690 |
rs113078112 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075344 | TTCATTTCAACTGTG[C/T]CCTTAATACAAGCCA | 57690 |
rs113079984 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071532 | AGCTGGGACTACAGG[C/T]GTGAGCCACCATGCT | 57690 |
rs113151269 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061047 | GAAGAATGTATATTT[G/T]AAAATTGAATGAAAA | 57690 |
rs113173537 | snp | C/T | 0.19646 | 0.2442 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056624 | GCCCGCCACCACGCT[C/T]GGCTAATTTTTTTTG | 57690 |
rs113180471 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028943 | TTGCACTTTACATGT[C/T]GGCGTGCAGAATTAC | 57690 |
rs113222455 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054818 | TATACACCACTGCAG[A/G]CTACTGTACGCTACC | 57690 |
rs113275437 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038407 | GGCTGGGTGCGGTGG[C/T]TCACGCATGTAATCC | 57690 |
rs113279642 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011189 | TTTTTTTAAAAACAA[C/T]TTTATTGAGTTATTG | 57690 |
rs113309711 | snp | C/T | 0.093777 | 0.195178 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099371 | TGATGAAGACATACC[C/T]GAGACTGGGCAATTT | 57690 |
rs113316767 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054798 | TGCAGACTACTGTAC[A/G]CTACTATACACCACT | 57690 |
rs113319332 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069541 | GGTGCATGCCACTCT[A/G]CCCAACTAATTTTAT | 57690 |
rs113347801 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107602 | CTCACGAGTGAACTC[A/T]GATTTTCCATTGTTT | 57690 |
rs113356418 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054550 | CAGAGCACTGTACAT[C/T]ACTGTGGACTACTGC | 57690 |
rs113475283 | in-del | -/TG | 0.275732 | 0.248672 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057825 | TCTGAATTACATTTT[-/TG]TGTGTGTGTGTGTGT | 57690 |
rs113519199 | snp | C/T | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022030 | TTCCTGTAGGTCTAG[C/T]CTTTGGGCCAAAAAG | 57690 |
rs113523751 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038412 | GGTGCGGTGGCTCAC[A/G]CATGTAATCCCAGCA | 57690 |
rs113554583 | in-del | -/AC | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069603 | CTTTGTGGCATTTAT[-/AC]AGTTTTGTATTGCAG | 57690 |
rs113569784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086717 | GAAAATTCCTGGGTT[C/T]AGCTAGGTTTGGGAG | 57690 |
rs113580560 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015843 | CTGGAACCCAGGAAG[C/T]GGAGGTTGCAGTAAG | 57690 |
rs113588386 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104995 | GGCCGCAGTCCTTGC[A/G]AACTGTTCGCAAAAC | 57690 |
rs113599202 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056303 | GCTGGGATTACAGGC[A/G]ATCACCACCATGCCT | 57690 |
rs113599732 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038776 | ACCAAATTGTCAAAA[C/T]TTTAAATCTTGTTAA | 57690 |
rs113620654 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101246 | CAGGGGCAAAATGCC[A/G]CCAGTCTCTTTGCTA | 57690 |
rs113671543 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029344 | TGCCATGTGATAGAA[-/C]CTTTTGCTCCTAGGC | 57690 |
rs113682865 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043385 | TTCTTAAGTAAAATA[A/G]CATTGTTCCAAATTG | 57690 |
rs113718210 | snp | C/T | 0.114036 | 0.209795 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038673 | GACAGAGCGAGACTC[C/T]GTGTCAAAAAAAAAA | 57690 |
rs113721986 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009945 | CTGGAGTGTAGTGGC[A/G]CGAACACAGCTCACT | 57690 |
rs113802527 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030484 | GCATCACCACAAACA[C/T]GTGAGTAATGTGTTG | 57690 |
rs113812311 | snp | A/G | 0.5 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052078 | ATCCCTGTGTCCAGC[A/G]GGACAAGGGCACTTC | 57690 |
rs113857642 | in-del | -/G | 0.204189 | 0.245767 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059855 | TGTCTCAAAAAAAAA[-/G]AAAAAAAAGAAAAAG | 57690 |
rs113880039 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108959 | CAGCGATCTTCCGAC[C/T]TCAGCCTCCCAAGTA | 57690 |
rs113891575 | in-del | -/A | 0.0341408 | 0.126114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028659 | TAGACTGGAGCTGAC[-/A]AATGTAAAGGGAAAC | 57690 |
rs113902342 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071626 | CACCTGGGCTCAAGC[A/G]ATCTGCCCGCCTCGG | 57690 |
rs113939739 | in-del | -/A | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106523 | CTGAAGATGTTATTT[-/A]AAAAAAAAAAAAAAC | 57690 |
rs113964086 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036819 | ACCCCAGCTACTCGG[A/G]AGGCTGAGGCAAGAG | 57690 |
rs113977025 | in-del | -/TT | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006829 | TTATTTATTTATTTA[-/TT]TTTTTTTTTTTTGAG | 57690 |
rs114068298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090365 | CTCCTATGGGCATTT[A/G]AATTTGCAGCCTCTG | 57690 |
rs114106008 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015017 | TTCCTTGGAATCACT[C/G]ATTATGTTGGCACAA | 57690 |
rs114106880 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005360 | CAAACAGGATCGAAC[G/T]GATAAAGTTGATTCA | 57690 |
rs114118808 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037815 | AACTTGATAGACTAA[C/T]TCCAAACTTCATCTA | 57690 |
rs114241857 | snp | C/T | 0.00338119 | 0.0409776 | missense | TNRC6C | GRCh38.p7 | 17:78051050 | CTTTAAAACCTGGCC[C/T]CCAACAGAACTGGGC | 57690 |
rs114242447 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039062 | TGACGACTGAATGCT[C/G]TGCATTTGTCCTCTG | 57690 |
rs114278850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072390 | CTAGAGTTGATGAAG[C/T]GAAAAATGCAGCTCT | 57690 |
rs114316674 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063477 | CTGAAGTTCACACCC[A/G]TGTTGTCAAGGGTCA | 57690 |
rs114324050 | snp | C/G | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067453 | ATTGCCACCTTCCCT[C/G]GTGGCCCCAGGATTT | 57690 |
rs114327149 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039157 | GAGTTGACTGTATTC[A/G]TTACAGAACAGGCAC | 57690 |
rs114407108 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066415 | AGCCACCACTCTGCT[C/T]AAAGTATTCCATTTA | 57690 |
rs114413374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096113 | AGTGCGCACGGCCGA[C/G]CTGACACCCTTTTAA | 57690 |
rs114421997 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092557 | TCTTCAAGGGTTTCA[A/G]TCTTTCAGGGCTGAA | 57690 |
rs114452758 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008639 | CACTCCTAAGGAGTC[C/T]GGGCATGTTTCTAAA | 57690 |
rs114546892 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021971 | TTCTATGTCTGATAG[C/T]CTAATATTACAAGTA | 57690 |
rs114732504 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014861 | CCACTTTGTATCCCT[C/T]CAGGACTGCTGATGA | 57690 |
rs114733385 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054739 | ACAGACTACTGTACA[C/T]TACTGGAGACTACTG | 57690 |
rs114767095 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030575 | CGGAACCACTGTCAT[A/G]TATGAGTCAGTTGTT | 57690 |
rs114795722 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016728 | ATTATTTAACTTCTG[C/T]GGCTTCCATTGCTTC | 57690 |
rs114842402 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026058 | ATTATTAGTGGAAGT[A/G]AATCCAAGTTTTTGA | 57690 |
rs114855731 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101218 | AAGTTGAAAGCTCCA[C/T]AAATCTCTAGGGCAG | 57690 |
rs114924892 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087612 | ACTTTACCAGCCACT[A/G]TCCTCCAGCCTAAAC | 57690 |
rs114949143 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039660 | GTTGTCAGGCAGCAT[C/T]CTGTGGCTGCCATCC | 57690 |
rs115001490 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015970 | TCTTAACCAGATTTC[A/G]GCTGAAGAATATAGA | 57690 |
rs115005793 | snp | A/C/T | 0.00139688 | 0.0263914 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093577 | CGTGAATCAATGTGC[A/C/T]GGTGTTCTGATCTGT | 57690 |
rs115007682 | snp | A/C/G | 0.0205591 | 0.0993414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038197 | AAATTTAAAAGTTTT[A/C/G]TACATGAATATGAAT | 57690 |
rs115065985 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089563 | GTAGTGGGGGCTCCT[A/C]GCTACCTTCCTTCCC | 57690 |
rs115124596 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032491 | TACTTTTGAAAAATT[C/G]ATGTACTGTAGTTTT | 57690 |
rs115230526 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051975 | CAAGGTCCAGAGTAG[A/G]GAGATTTTAAGGTGG | 57690 |
rs115245526 | snp | A/C/G | 0.0079133 | 0.062403 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091434 | TAACCGCATCTCTCT[A/C/G]TTTAGCTGGACTGAA | 57690 |
rs115259128 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022527 | CATGGTGGAAAAGCA[C/T]GGTCAGAGATGTGAG | 57690 |
rs115263506 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006690 | TCTTCATCATTGTCA[C/T]TGTTTTCTACTCAAG | 57690 |
rs115278734 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020273 | CTGTGAGAACAAGTA[C/T]GTGGGTAAACTGAGT | 57690 |
rs115361584 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062656 | ATTAGAATTTGAGTT[C/T]ATTTGGAAAAATAAA | 57690 |
rs115396312 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103139 | TCTGTGCGACGTGCT[C/T]TGGTGAAAGGAGAGC | 57690 |
rs115400176 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076840 | CACCTAGAGCTTTGG[A/T]AATAACTTCTCAAAA | 57690 |
rs115428692 | snp | G/T | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029253 | TGCTTGACAGAGAGA[G/T]ACGTTCTGAAAAATG | 57690 |
rs115454572 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054439 | GCAGACTACTGTAAA[A/C]CACTGCAGACTACTG | 57690 |
rs115463145 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097088 | GGTGTGGTGGCATGC[A/C]CCTGTGGTCCCTGTG | 57690 |
rs115495590 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017297 | TTGAATAAGATAGAA[A/G]CACCTCAGCGTGCTC | 57690 |
rs115558050 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017444 | ACCGCTGCCTCCTCT[C/G]CCAACCACATGGCTC | 57690 |
rs115609146 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018997 | CAGAGCTCATTGCTG[G/T]TTCTGAGACTACATG | 57690 |
rs115657211 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042728 | ATGGTGGAGATAACA[A/G]TGATGGTAGTGGTCA | 57690 |
rs115658238 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074392 | TTAGCAAGTAGGCCA[C/G]CTTTACAAGTACAGA | 57690 |
rs115659881 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004061 | TCAGAGGGTCCTCCT[G/T]TATACCATATGCGAA | 57690 |
rs115714987 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006389 | GGTACATAGTTGTGT[A/G]TGAATTTATGATCTT | 57690 |
rs115722453 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094062 | TCAGCTCTCTGCAAT[C/T]TCCACCTTCTGGGTT | 57690 |
rs115780503 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021196 | GGCATCAGTAGCACA[C/G]AAATGATGGTCAGAA | 57690 |
rs115892959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016556 | CTTTCCAAACTGTTG[A/G]AGATATGGGAACCAA | 57690 |
rs115941189 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066802 | CGGGCTTGTTAGAAA[A/T]GCAGCCTGTCGGGCC | 57690 |
rs116052915 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030817 | AGAAATGCAAATTCC[A/G]GCCGGGCATGGTGGC | 57690 |
rs116062765 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011279 | CCATCACCATGATCA[A/G]GATGACACCCATCAT | 57690 |
rs116152967 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025801 | AGTATTTCATGTCTA[C/T]ATCAAGGCCAGGGAA | 57690 |
rs116171095 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057859 | GTTTTAAAGGAACGA[A/G]TGCTACAGTACAATC | 57690 |
rs116177480 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032821 | CTGTGACTTTGTAGT[A/G]TAGTCAGAACTAATA | 57690 |
rs116269464 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029227 | TAAAATTCAGTAGTA[C/T]GATCATACCTTGCTT | 57690 |
rs116286532 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107416 | TTTCGAAAGTACAAC[A/G]CTTTATTGAATCTTA | 57690 |
rs116319099 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036280 | AGAAAGTGAAGTATT[C/T]GTGGAAGGAATTGAC | 57690 |
rs116321347 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073769 | TTCTGTTTCAAGACA[C/T]CTTATTTAATATTGA | 57690 |
rs116386350 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037302 | CATGTGTGTCTTCAT[G/T]TGTTCATTGAGCAGA | 57690 |
rs116434015 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053928 | ATGCATAGCTTAACA[A/G]TGGTGATACATTCTA | 57690 |
rs116466326 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066724 | TGAAGTGGAAACTCG[A/G]TAGTCACTTTGTAGC | 57690 |
rs116484568 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079258 | TGTCTCAAAAAAATT[A/C]TCTTGGGTACAAGTT | 57690 |
rs116488867 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039675 | CCTGTGGCTGCCATC[A/C]CTCGTGGGAAACACA | 57690 |
rs116542855 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017966 | GAATCCCTAAATTAG[A/G]TTATCTTGTCCCACT | 57690 |
rs116550808 | snp | A/G | 0.00506157 | 0.0500516 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067718 | ATTGTCTGCGTTAGG[A/G]ACATGAATTTGATAA | 57690 |
rs116605560 | snp | C/T | 0.0494327 | 0.149241 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109127 | TTGTTGTTGTTGTTG[C/T]TGCTGCTATTTTGGC | 57690 |
rs116606355 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098883 | GCACAGCGCTTTAGG[A/C]TCTCTGCCCCCATGA | 57690 |
rs116630991 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020355 | TACATGCTTTGTGGC[A/C]TTTTTTTCTGTTTGT | 57690 |
rs116633118 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032330 | GCCCTGCTTCTTGTT[G/T]CTTCCTTGCCTGTAA | 57690 |
rs116634351 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076088 | GAGCATGGTGGCACA[C/T]GCCTGTGAACCCAGC | 57690 |
rs116732753 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059877 | AAGAAAAAGAAAATA[C/T]AGTGTGCCCCCCGCC | 57690 |
rs116750198 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009858 | GCCCCTGGCCTGAAT[A/T]ATGATTTTTAAGTCA | 57690 |
rs116802144 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078139 | CTTCCACTCACCAGC[A/G]CCCGACTGTGTGATC | 57690 |
rs116841308 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052646 | GTTTTTGTCATAAGC[A/G]TTCAACAGGAGAATG | 57690 |
rs116881664 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080933 | TAAAATTTAATTTAA[A/C]TGTGTTTAGTTTGTT | 57690 |
rs116911628 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053809 | GGCTGAGGTGGAAGG[A/T]TGGCTTGAGCCCAGG | 57690 |
rs116974863 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020722 | AATATCGCCATTTCA[A/G]TGTGAAAGCAACAGA | 57690 |
rs117027750 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003554 | AAAATAGAAGCACCA[A/G]TAAAAGAGTAGAAAA | 57690 |
rs117030621 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062292 | AGCTTGTAATTTAAA[A/G]TGATTTTTAGGTTGC | 57690 |
rs117114166 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089789 | TGAACCTCAAATGAT[A/T]GGATAGGATTACAGT | 57690 |
rs117177391 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057743 | CACTTATGTCAGAGT[C/T]TGGGTTTTAAGTTGT | 57690 |
rs117299172 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077696 | TCATGGCAACCAAAA[C/T]GACGTTACATCTGTT | 57690 |
rs117311452 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034842 | GACATGGTGGCATGT[A/G]CCTGTGGTCCCAGCT | 57690 |
rs117323783 | snp | A/G | 0.000435737 | 0.0147539 | missense | TNRC6C | GRCh38.p7 | 17:78091484 | AGCATGGACATGACC[A/G]GTGGCTTGTCGGTGA | 57690 |
rs117351878 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105973 | TATACCTACCTTTAG[C/T]AGCTTTTTATTGTGG | 57690 |
rs117389735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070680 | TGGAATAAACCCCCT[C/T]ATTTTATCATTTTTC | 57690 |
rs117429831 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058350 | CATACTCAGACATAA[C/T]ATTCTGGGACACTTA | 57690 |
rs117481081 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012553 | TAGTGGGAAGAGCCA[C/G]GCAGATAAGCAAATA | 57690 |
rs117607986 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077024 | TTTCTTTTTCTTTTT[C/T]CCCTCTTCCTTTTGC | 57690 |
rs117640390 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016155 | TAATTGAGAGGCCCT[A/G]TTGGCTCTCTTGACT | 57690 |
rs117678822 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088160 | GTAATCATATGAATC[C/G]TTTTTACTTGACATA | 57690 |
rs117862021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093384 | ACACTGCACACTATC[C/T]GGTAAAACTATTCCA | 57690 |
rs117887293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076085 | AGCGAGCATGGTGGC[A/G]CACGCCTGTGAACCC | 57690 |
rs117963883 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084351 | AAAAGAATGGGAACT[C/G]CAAAAGACAGAACCA | 57690 |
rs117974169 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093305 | TGGGTATGGTTAGCA[A/T]CAGGCATTTTTCTGT | 57690 |
rs118000745 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095072 | GCATATTTTGAGGGA[C/T]GTGGAGAAGTGGGAT | 57690 |
rs118080372 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047528 | TATTAGCTTTAGTAT[A/G]GTCTTTCTAATGCTA | 57690 |
rs118089521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086781 | AAGACAATGAAGAAT[A/G]CATTTGGTCCCTAGA | 57690 |
rs118131105 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002380 | CTCATAATCTCATTT[A/G]AAGCCAGGACATGTG | 57690 |
rs118172956 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006873 | TCTATCGCCCAGGCT[A/G]GGTGGAGTACAGTGG | 57690 |
rs137865291 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088022 | AGGACAAAGGGTTAT[C/T]GGTAACTTGGAAAAT | 57690 |
rs137886536 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053268 | ACTAATATTTCTAGG[C/T]CCTTACATTTTATAA | 57690 |
rs137888798 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028638 | GTTGAGAGACAAAAA[A/C]TGCAGGTAGACTGGA | 57690 |
rs137903929 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005463 | ATAATAAAAAAGATA[C/T]ATTCTTTCTGGATTC | 57690 |
rs137963172 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056120 | CTCCCAAAGTGTTGG[A/G]ATCATAGGTGTGAGC | 57690 |
rs138004382 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092361 | CTGTATGAATTTTTA[A/C]CATCCACTGTGTTCT | 57690 |
rs138084511 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091757 | TTATAGTGCATATAA[C/G]ATCTCAGCTAGTCAC | 57690 |
rs138100590 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031776 | CAGGGTGCTGGGCCT[A/G]CAGGGGTAAGCCCAC | 57690 |
rs138112797 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060976 | TCTCTGTCTGCTGCT[A/C]ATTTTTATACCCAGC | 57690 |
rs138122764 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094955 | AAAGGAGCCGTGTAA[A/G]ATGGCAGAGGACAGG | 57690 |
rs138135082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035047 | AACTAGAACTTGTTA[C/T]GCCACCAACTAGTCC | 57690 |
rs138153476 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084439 | CTGTTTTTTAGACAC[A/G]TGTCCAACAAGTTTG | 57690 |
rs138163020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044706 | GCACACAGCCACACT[C/G]ATTCTGCTTTTGTGC | 57690 |
rs138168981 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002922 | AGGAAAAGAAGTGAT[G/T]AAAATAGCTTAGAAG | 57690 |
rs138185629 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101766 | AAGGCACAGATCGCT[C/T]GTGCTACTGTTTGTG | 57690 |
rs138218670 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068898 | TCTCATTTTTTTCTA[G/T]ATGACTGCCCAATTC | 57690 |
rs138233669 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096287 | GGTGGGAGGAAGGAG[A/G]GGATTCAGAAACTGC | 57690 |
rs138239660 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011343 | ATCTCCTCTGTCCCC[A/G]CCCTACCCCCATCTG | 57690 |
rs138243441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035362 | GTACTTTTGACTCAT[C/T]TTTGAAATGAAGAGA | 57690 |
rs138251989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083554 | CAGATTTTATAATTA[G/T]GCATGTCTTTTCAGT | 57690 |
rs138260502 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024776 | TGTGGAACATTTGAT[A/T]CAACTGATGTTCTAG | 57690 |
rs138271532 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020394 | GTGCTAGTACTTTAG[C/T]GTAGAGTAAATAGTT | 57690 |
rs138276293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073729 | TTTGTCAACCAATCA[A/G]TATATAACCTTGTTT | 57690 |
rs138278946 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014482 | TTAAAAAGAACTTAG[A/G]TGTGCTTGCATATAT | 57690 |
rs138367350 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072937 | TTTCCAGTTCCAAAA[C/G]CTAATAACTATGTCT | 57690 |
rs138454580 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105261 | AGCCTGTGACGATTA[C/T]GCACATGACCAGAGG | 57690 |
rs138478334 | snp | C/T | 3.55341e-05 | 0.00421495 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049137 | TAATGGCACCAATGG[C/T]GCACTCGTCCAAAGC | 57690 |
rs138484209 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109044 | TTTTGTAGAGATAGG[G/T]TCTCACCATGTTGCC | 57690 |
rs138494241 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099889 | TTAGTTACTTCCTAG[A/T]TACAATGGGGGTACA | 57690 |
rs138537799 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025149 | CACTCTTTGTGTTAT[A/G]TATCTATGGGTTTTG | 57690 |
rs138580234 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003165 | ATTTGAGGTTGGACT[A/G]GTAAAACAGCCAGTT | 57690 |
rs138620988 | snp | A/G | 0.133435 | 0.221162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028100 | AGACAGGGTTTCACC[A/G]TGTTAGTCAGGATGG | 57690 |
rs138624950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087768 | CAAATCAACATATAT[A/G]TGTTGAAATCTAACT | 57690 |
rs138638479 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034836 | TAGCCAGACATGGTG[A/G]CATGTGCCTGTGGTC | 57690 |
rs138674463 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091659 | GCTGGCTTATTAATC[G/T]ATCGTCCTGTTGTAT | 57690 |
rs138729702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016580 | GAACCAAATTAAGGG[A/G]GGTGGTTTAGAACCA | 57690 |
rs138789773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061368 | TAAAATCATTTTCTG[C/T]GTGCTGAAAATACTT | 57690 |
rs138792901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073556 | TAGAGCTGCTTTAAT[A/C]ATAATGTTAAATATT | 57690 |
rs138813385 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038446 | TGGGAGGCCGAGGCA[G/T]GTGGATCACGAGTTC | 57690 |
rs138814218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076336 | CTCAGCTGCAGCTGT[C/G]GGGTAGCCCAGGGTG | 57690 |
rs138828694 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029131 | ATTCATTATTCGCAC[A/T]GTAGGCCCAACTGCA | 57690 |
rs138834095 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064013 | TAAAGTTGAAAATAG[G/T]TAGAGGGCAGGAGTT | 57690 |
rs138858193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065020 | GATTAGAGTTTTAGG[A/G]TACTTTCCTCATTAT | 57690 |
rs138882876 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052527 | TTGGGCAGTGATGGT[A/G/T]CAGGGAGGAAACAGT | 57690 |
rs138894108 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042420 | TTCATCTGTAAAACT[A/G]ACATTGTTTGTAAGG | 57690 |
rs138937854 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102132 | CTGATTCCACACCGG[G/T]TCTGGGGACAGGCAG | 57690 |
rs138974421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030600 | GTTGTTGACTCAAAC[A/G]TCATTATTTAGCTTT | 57690 |
rs138986862 | in-del | -/TG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030314 | CCACCACACCTGGCT[-/TG]TGTGTGTGTGCGTGT | 57690 |
rs139030959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069994 | TGGCATGAGATGAAA[A/G]CTTTCTTTATACCTT | 57690 |
rs139042882 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018543 | TATTGACATGTTTGG[C/G]GGGGTGGAGCAAATG | 57690 |
rs139045780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078159 | ACTGTGTGATCCTGG[C/T]GATCTGACATTGCCC | 57690 |
rs139060581 | snp | C/T | 1.8244e-05 | 0.00302021 | missense | TNRC6C | GRCh38.p7 | 17:78050191 | AACCCTACCGTACAG[C/T]CTGGTGGTGAACACA | 57690 |
rs139091247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100523 | AGTCACAACTGGAGC[A/G]GCTGGGACACAAGGC | 57690 |
rs139109836 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066382 | TGTTTTGCTAATACT[C/T]GATAGTATGTTCCAT | 57690 |
rs139118053 | in-del | -/AC | 0.497855 | 0.0326773 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029809 | TTATTAAAAACCTAG[-/AC]ACACACACACACACA | 57690 |
rs139132079 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054594 | CTACTGTAGACTACT[A/G]TACACCACTGCAGAC | 57690 |
rs139151790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022233 | TCAAGGTGGAAAGGG[A/G]AGACTGGTTAGGAAT | 57690 |
rs139199521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103930 | TCCAAACGTAGTCAC[A/G]TGGGGAGGTACTGGG | 57690 |
rs139213672 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077794 | GGTTCTCAGGAGTCA[C/T]ACTGGCATTTTTTTC | 57690 |
rs139225947 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018283 | AGGTGTGCATCACCA[C/T]GCCCGTCTAACTTTT | 57690 |
rs139236352 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030002 | GTTTTACAGTTAACT[A/G]TTGTTTTTGGCTTTT | 57690 |
rs139249538 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081111 | CCGTTTCTCATAGAT[C/G]GCAACTTTTATGCAT | 57690 |
rs139254938 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079121 | AGGCATAGTGGCGGG[C/G]GTCTGTAATCCCAGC | 57690 |
rs139263768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021155 | GCTGGACTTGGAGCT[C/T]GAGGGCAACACTGGG | 57690 |
rs139425192 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062429 | TGATATTGTAATATC[A/C]ATGTTGAGGCCAAAC | 57690 |
rs139433944 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038611 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 57690 |
rs139436923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046366 | TTGTGTAAGTAGAGA[C/T]GAGGTTTCACCATGT | 57690 |
rs139466686 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046204 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTGTGT | 57690 |
rs139480453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065510 | GTTTGATTCTCCTGG[C/T]AATACCCACACTACT | 57690 |
rs139499422 | in-del | -/AGC | 0.0376037 | 0.131863 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017565 | TGGGTTAACAATTGT[-/AGC]TAGCAACCTGTCTCT | 57690 |
rs139533145 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036797 | GGTGTGATGGTAGGC[A/G]CCTGTAACCCCAGCT | 57690 |
rs139536130 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098248 | TCACACAGTCTGCTG[A/G]TGTTAGAGAGCACTC | 57690 |
rs139550552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025956 | ATTAGAAGGAGCCTT[A/G]GAGTGTCAGCTAGTC | 57690 |
rs139554719 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085682 | CAAATCTGCATTTCA[C/G]GTTCTCTCTTAGCTT | 57690 |
rs139594324 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103001 | TTTTTTAAAAGAGTC[A/G]TTTGGCCACATCAGA | 57690 |
rs139598639 | in-del | -/TC | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018999 | GAGCTCATTGCTGTT[-/TC]TGAGACTACATGTGG | 57690 |
rs139607667 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008673 | GGAGGCCTTTTCCTT[A/G]GTTGTCTCAGAGTGT | 57690 |
rs139653937 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093877 | CAAGGCACAGTTGGC[A/G]GGCACCTTTTCTAGT | 57690 |
rs139678532 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058177 | CTACCTTGCGCTCTG[C/T]TGTGCATACAAAGCT | 57690 |
rs139699953 | in-del | -/AA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064318 | GCCAGACTGGTCTCG[-/AA]CTCCTGACCTTAAGT | 57690 |
rs139754541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097475 | TTTTAAGCATTCTGG[C/T]GGGAATTCTCAAAGA | 57690 |
rs139785939 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003845 | AGGGCAGGAGATCGC[C/T]TGAGCCCAGGTATTC | 57690 |
rs139895691 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106274 | AAAAAAAAGACTTCC[A/G]TCGTAAAGAAACCTA | 57690 |
rs139967258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092754 | AATAAATAAATAAAT[A/G]AATAAAGTCATTGAT | 57690 |
rs139996362 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053607 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAAACTC | 57690 |
rs139997187 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019191 | AAAGAAGCAGAGAGA[A/G]TGGGGTTGCAGCCAG | 57690 |
rs140006046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035886 | TAAAAGCTCTTATCA[A/G]CTTTCTTAAAAGTAA | 57690 |
rs140006476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057684 | GTTGGTGTTTTTAGG[C/T]TTTATTCAGCATAGG | 57690 |
rs140023949 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093386 | ACTGCACACTATCCG[A/G]TAAAACTATTCCAAC | 57690 |
rs140031818 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011602 | TTCATGGACATCTGC[A/G]TTTTTCCAGTTTTGA | 57690 |
rs140050019 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060784 | AAGGACTGCCCATCA[C/T]ACTTATAAAGCTATG | 57690 |
rs140062760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78002208 | TAAAGTTTTCCTTAA[A/G]AGGAAAACTTACAGA | 57690 |
rs140067281 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011774 | CAGCTCTTTCCCAAC[A/G]TGTTTATACTGTTTC | 57690 |
rs140085332 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014981 | GTATAGGCTGCAGAA[G/T]AAATTGTAATAACAA | 57690 |
rs140115840 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063138 | GTAGTCCCAGCTACT[C/T]AGGAGACTGAGGCAT | 57690 |
rs140176090 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065911 | TATTAACATGAGTAT[A/G]AGATTACTGATTTAA | 57690 |
rs140195695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033537 | AGCTGGGCATGTTGG[C/T]ACATGCCTGTAATCC | 57690 |
rs140250007 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103277 | GTTAATGTTGTAAAA[C/G]CACATATTATTAGGC | 57690 |
rs140256900 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083282 | GGGATGTCATTGAGA[-/CT]CTCATGAAGTATTTA | 57690 |
rs140277389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087787 | TGAAATCTAACTTGT[A/G]GAAGCACACTCAGCA | 57690 |
rs140297760 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090467 | TGGCGTAGTACTTAC[G/T]GTAAGGACCTATGGG | 57690 |
rs140306247 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012262 | TAATTAACTTAAACA[C/G]TTAATAAATACCTGT | 57690 |
rs140306859 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030242 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 57690 |
rs140390947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044091 | ATTGAGGTAGTATAA[C/T]TTATTATCAAACCCT | 57690 |
rs140391860 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105673 | GCGCGTGCTCCTGCA[C/T]GGCGTGCAGTTTTCT | 57690 |
rs140403697 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094692 | TGATCCGCCTGCTTT[A/G]GCCTCCCAAAGTGCT | 57690 |
rs140406726 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012528 | GTTCCCTGTTCTCAA[A/C]GAGATATTTTAGTGG | 57690 |
rs140433035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074106 | TTTCCTCTGTAAGGC[A/G]CTTTACTGCCTTCTT | 57690 |
rs140447583 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015558 | CCATTACTGGGAAAC[A/C]GTGGTATACCTAGCT | 57690 |
rs140466417 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042789 | TGCTGATGGTGGTGG[G/T]GGTGGTGTTGGTGAT | 57690 |
rs140473668 | in-del | -/C | | | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78075223 | CAAGCCCCTCGGCTG[-/C]CCGCCCGCCAATCTC | 57690 |
rs140492926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020217 | CAGGATGACCTGTAG[A/G]CTACCAGCCATAGCA | 57690 |
rs140497179 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079841 | GACCTGCCCAACACA[C/T]TCCCATTGATGTGCT | 57690 |
rs140527335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055760 | CTGGCCATGGTTGGC[A/G]GTCATGTATGGAGCA | 57690 |
rs140595295 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101573 | GGTGTGAAGTGGGAA[A/G]TCGGGGGTCTCACAG | 57690 |
rs140600551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024711 | TCGAGCTGAAAGTAT[A/G]AAGTTCCCATGTATT | 57690 |
rs140607658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041761 | TGAAAACCAAGCAGC[A/G]AAGGATTTGTGGTAT | 57690 |
rs140619816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104178 | ACATCACTTGAGACG[A/T]TGGAACCTAGAAATT | 57690 |
rs140630411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044454 | GAATAGGTACGCCTT[A/G]CCTTCATGGTGTTTA | 57690 |
rs140653655 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030364 | AGACAGGGTTTCACC[A/G]TTTTGGCCAGGCTGG | 57690 |
rs140667530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090817 | TTGATACTTAATTCA[C/T]AGACTCTTTCAGAGC | 57690 |
rs140677361 | in-del | -/C | | | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78086939 | GTGAAGCAGCCACCA[-/C]CCGCCACCGCCCCCG | 57690 |
rs140725095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027020 | TTGATTTTGAAGTGT[A/G]TCAAGTATAAAAGAG | 57690 |
rs140809537 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086661 | GCTAATTGATGAACT[A/G]TTAGATGATCATTGA | 57690 |
rs140851050 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089036 | GCGATGGCGCAGTCT[C/T]GGCTCACTGCAACCT | 57690 |
rs140869322 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029462 | GGGACAAGAAAAATA[C/T]GCTATAAAGAATTTT | 57690 |
rs140880309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075481 | TACTGAGAATGAAAA[A/T]GACTGGGATTGAAAA | 57690 |
rs140942053 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059232 | GATCCCATTGACCTC[G/T]GCAGCCAGAAGTAAT | 57690 |
rs140982053 | snp | C/G | 0.0228947 | 0.104514 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012753 | ACAATGTTGGCAGCA[C/G]AGGAGCTGCTGAGTG | 57690 |
rs140982111 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047018 | TGGAAAAGAATGCAT[C/T]GGTCAGCCAGGTTGT | 57690 |
rs140985481 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047316 | GGGTTATAGAGCCAA[C/T]CCCTAATAATTGGCA | 57690 |
rs141003240 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099134 | GTGGGCAACAAAGTG[A/T]GACCCCATCTCCACA | 57690 |
rs141006272 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016234 | TAACACTGTCTCTCT[C/G]AGCCACAAAAGGAGC | 57690 |
rs141021996 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087357 | TCCTGGGCTCAAGCA[A/G]TCCTCCCACCTCAGC | 57690 |
rs141094816 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052201 | TTTCTCTCTGGGAGT[A/G]TGAATACTAGCCCAG | 57690 |
rs141190761 | snp | C/T | 0.0277411 | 0.114461 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049725 | CATCATCCCGCCCCA[C/T]CTGCAAGGCCTTCCT | 57690 |
rs141211079 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018453 | TTTTTTTATATAATA[C/T]TCAGTATTCACAGTG | 57690 |
rs141233713 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006622 | TTCCTTCTTCTTCTT[G/T]CTTCTTCTTCCTTCT | 57690 |
rs141255887 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104279 | TCACGCACTTGAAGA[A/T]GTACTCTGTGTACCA | 57690 |
rs141285789 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107916 | GCATCTATTTTTGTA[A/G]AATCACCTTCGCTAA | 57690 |
rs141286747 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088709 | GCCTTAAGTGATCCT[C/G]CTGGTCTCAGCTTCC | 57690 |
rs141304583 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075966 | TCACTCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 57690 |
rs141327059 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054314 | CACTACTGCAGACTA[C/T]GCACACCACTGCAGA | 57690 |
rs141335448 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027989 | CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT | 57690 |
rs141416910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030191 | GTCTCGCTCTGTCAC[C/G]CAGCCTGGAGTGCAG | 57690 |
rs141437837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067672 | GCATCATTTGTCCCA[C/T]GACCCCTAAATTATA | 57690 |
rs141438342 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062188 | TGTAATTAAAGGTAA[C/T]ATTATAGTTAGCAAT | 57690 |
rs141474678 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071891 | AAGTTTCCAGTCATA[A/C/T]GTAGGGAGAATTCAT | 57690 |
rs141476606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034924 | CAGTGAGCCAAGATC[A/G]AGTCACTGCATTCCA | 57690 |
rs141495844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051877 | ACATGCCCATGAGCA[C/T]AGCAGGAGGCACAGA | 57690 |
rs141577744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096717 | CCAGGATACGTGCAC[C/T]GGCAGAGTCATTGTC | 57690 |
rs141586160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073579 | TAAATATTTACATTT[A/G]AATATAGTCGATTCT | 57690 |
rs141594376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014808 | TGTTGCCACGGTGAT[A/G]GATCAGCCAGAAGCA | 57690 |
rs141632456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028127 | ATGGTCTCGATCTGA[C/T]CTTGTGATCTGCCCG | 57690 |
rs141681703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021770 | AGATGGGGTTTCACC[A/G]TGTTGGCCAAGCTGG | 57690 |
rs141710848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035060 | TATGCCACCAACTAG[C/T]CCTTCCATTTCTCAT | 57690 |
rs141755697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057445 | TTCATAGAGGTGACA[A/G]CATGCAGGAGTGGCA | 57690 |
rs141774944 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025572 | AGGTTTTTGTATGAA[C/T]GTAAAGTTTTCAACT | 57690 |
rs141832402 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082799 | TATAGGCTCTCTGCA[C/G/T]GGGGAAGCACATCAC | 57690 |
rs141854287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082136 | TTTGTTCCCAGGCAG[A/G]TTGGCAGGTCGAGAA | 57690 |
rs141868560 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022191 | TTACTTCACCTGCCA[C/G]TCCTGCCCTACTCAC | 57690 |
rs141871870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086731 | TCAGCTAGGTTTGGG[A/G]GGAGGTTGGCCTAGC | 57690 |
rs141873668 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048597 | TAACGTGCATTGTGA[A/G]TATTCTCCAGGGGGA | 57690 |
rs141899324 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038324 | AGAAGAATGGGCAAA[G/T]AATGTGAACGGGAAG | 57690 |
rs141912154 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066886 | AGGTTTGAGAAGCTC[C/T]GGTCTGTGTGACTTA | 57690 |
rs141932937 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009697 | GTAGCTGGGACTACA[A/G]GTGCGCACCACCATG | 57690 |
rs141994894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077602 | CTAACTTGGGACTGG[C/G]TAAAGTGATGATGTG | 57690 |
rs142018406 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042310 | GTTGTGGTGGGAAGA[A/G]CACTAGATTATATTC | 57690 |
rs142059065 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089152 | TTTGTATTTTTAGTA[A/G]AGACTGGGTTTCACC | 57690 |
rs142072889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010872 | GGTAAAAATGTATTG[C/T]CAGAACCTCTGAGTA | 57690 |
rs142082487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012432 | ATAATCTGTACATCA[A/G]GCCCCCCATGACATG | 57690 |
rs142117456 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100438 | GAGTCTCAACACCAC[A/G]TGGAAGCTGCCAAGG | 57690 |
rs142221716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043579 | TGTGTTACAAATAAT[C/T]CTATTATACTCTTTT | 57690 |
rs142225577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103353 | ACGTTTTTTCTTTGG[A/C]AGGCTGTAGTGAAAG | 57690 |
rs142249940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098707 | CCAGGGCAGTAGCTG[A/G]GTGAGCCTGGTGTTT | 57690 |
rs142266032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036226 | ACGTAAACTCTTTGT[A/G]CCCTCCCCCCAGGTT | 57690 |
rs142288406 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063834 | ATAATATTTCAGTAT[A/G]TATTTGCAACTCACA | 57690 |
rs142288672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101175 | GCTTAGAAATTTCTT[A/C]TGCCAGATACCCTCA | 57690 |
rs142302969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005511 | ATGTAAAAGATTTCT[C/G]TTTTTATCCTCCAAG | 57690 |
rs142311730 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053317 | GAGAAGCAGGAAGAA[G/T]GAAAATGAAGGGATT | 57690 |
rs142318484 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082587 | AGGGAGTATGCCTTA[A/T]CCCTAAAGAGACCTA | 57690 |
rs142326725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024429 | TGGAGTGCAGTGGCC[C/T]GATCTTGGCTCACTG | 57690 |
rs142330341 | snp | A/G | 0.000984844 | 0.0221687 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051402 | CGAGACGCCGCCCCC[A/G]CACCAGGCCGGTACT | 57690 |
rs142348778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019899 | CCCTGGTTTTTTAGA[C/T]AGTAATAGACCCATA | 57690 |
rs142381243 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008340 | ATCTTTTCAAATTCT[A/G]ACCTGTGATATCTTT | 57690 |
rs142418097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090060 | GAAAAGAACCCACAC[A/G]GCAGAGATTGCAAGT | 57690 |
rs142438156 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055531 | ACTAGGTGATGGGAA[A/T]TTTTCAGCTCCATTA | 57690 |
rs142493895 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025082 | AGGCATGAGTCACCG[C/T]GCCCGGCCAATACAT | 57690 |
rs142563630 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070885 | CATATATACCAACCT[A/G]CAAATGTACCTTGAT | 57690 |
rs142649375 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084692 | GGAGTGCAGTGGCAC[A/G]ATCATGGCTCACTGC | 57690 |
rs142658612 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106131 | CCGTGGAAGGAACAG[A/C]AACAAGCACTTGGGC | 57690 |
rs142660251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020625 | ATGTGAGCCACATGA[A/G]TCATTTTAAATAGGC | 57690 |
rs142685428 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088424 | TTTTTGGTAGAGACA[A/G]GGTCTTTCTATGTTG | 57690 |
rs142685898 | snp | A/G | 0.000762499 | 0.0195107 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050286 | TGGCAACCACAATGA[A/G]GGAAGCACTGGGAGG | 57690 |
rs142689353 | in-del | -/CTTCCGACCAGCGAG | 0.23031 | 0.249223 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108950 | TTAAGCTCCAGCGAT[-/CTTCCGACCAGCGAG]CTTCCGACCTCAGCC | 57690 |
rs142696689 | snp | G/T | 0.000770119 | 0.0196078 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075129 | GCTTCTGTTTGTTGT[G/T]CTCCAGGCGCTCTGC | 57690 |
rs142716429 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015739 | CAAGATGGCAGAACC[G/T]CATCTCTACTAAAAG | 57690 |
rs142719203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011443 | GGGACTCCTACACTG[G/T]GCACTTTGGCTCCTT | 57690 |
rs142753763 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033463 | TCACCTGAGGTCGAG[A/G]GTTCGAGACCAGCCT | 57690 |
rs142765153 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077893 | TGAGAGTGTTGTTTG[C/T]CACTTCATCTCACTT | 57690 |
rs142782295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029228 | AAAATTCAGTAGTAC[G/T]ATCATACCTTGCTTG | 57690 |
rs142785090 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064137 | CAACCTCTGCCTCCC[A/G]GGTTACCAAAGTATA | 57690 |
rs142804453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069390 | CCACAGAAAGCCAGC[A/G]TTTTGATTTTTTTAT | 57690 |
rs142845572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014522 | TACATTTTCTTACAG[C/T]AGGAATATCCAAGGG | 57690 |
rs142853561 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082400 | GAATTTACAATATAG[G/T]GTGTGCATCAGCAGT | 57690 |
rs142874146 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047263 | TATTATATTAGATAG[C/T]TTTTAGAGTATGTGC | 57690 |
rs142959456 | snp | A/C | 0.000893966 | 0.0211231 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087017 | CTTCCCCTCGCACCC[A/C]CAGACTCCCGGCCTA | 57690 |
rs143043500 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094361 | AATAAGGCCACCTAG[A/G]TAGTTCCCAAAACAT | 57690 |
rs143053137 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034601 | TGCACTTACTGTATA[C/T]TGTATATCCTATATT | 57690 |
rs143084903 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065664 | CCTAACGCATCTTGC[C/T]GTATTGCCCTGCTTT | 57690 |
rs143111093 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092380 | CCACTGTGTTCTTCC[A/G]TAGTGAGGGTTTCAG | 57690 |
rs143126039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072339 | CTACTTGTTTTGTTT[C/T]TCTGTTTCTTAGAGA | 57690 |
rs143146413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038265 | AAGATAAATATCTCA[A/G]AAATACCAAGTGTTC | 57690 |
rs143169840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042485 | ACTCCGAAATGGTAT[A/G]AAGTATGTGATGTCT | 57690 |
rs143170321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081242 | CTCTTAACACCACCA[C/T]AATTAGGGTTTGGGT | 57690 |
rs143234660 | snp | C/G | 0.000155087 | 0.00880451 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104443 | ACGAACTCAGCAGGA[C/G]TTGGGGTGGCCCTGT | 57690 |
rs143262310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014732 | TCTCATTAGCAACAG[A/G]CACTAAGTTAATGTA | 57690 |
rs143277110 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063177 | CTTAACCCGGGAGGC[A/G]GTGGTTGCAGTGAGC | 57690 |
rs143314740 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045491 | GTCTGAGTAGGCGGC[A/G]TCATTGTAGTGGAAG | 57690 |
rs143335497 | snp | A/G | 0.000912114 | 0.021336 | missense | TNRC6C | GRCh38.p7 | 17:78049486 | ATGGGCAACCAGAAC[A/G]GGAACCCAACAGGCA | 57690 |
rs143363170 | snp | A/C/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106358 | CCCTCGGCCATCGTC[A/C/G]TGGACTCTGTCGATT | 57690 |
rs143398910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045182 | GGGAAGAGACCTGTT[A/G]GAAAGTTATTTACAG | 57690 |
rs143422951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015935 | ATAAATAAAACTCCT[C/T]GCTAAAAAAGTCTAT | 57690 |
rs143459127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063474 | TCACTGAAGTTCACA[C/T]CCGTGTTGTCAAGGG | 57690 |
rs143461807 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019215 | CAGCCAGGACTTGAA[A/G]AGGCTCAGACCCTAG | 57690 |
rs143484229 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052986 | CCAGATTTCTGGCTT[C/T]CTTTGGAAACCTGAA | 57690 |
rs143546409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101431 | CCCGTCTATTTCTGA[A/G]CCTTGAGTTCCAACC | 57690 |
rs143546626 | snp | C/T | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003785 | AAAATAAAGCATGGC[C/T]AGGCTTGGTGCGTCA | 57690 |
rs143547675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045919 | GCTTCAGGGCTCTCT[A/G]TTTTAAAAATGTTAT | 57690 |
rs143567593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068149 | TCTCTCCGGTATAGG[A/G]TAGAGGTGTCCAGAG | 57690 |
rs143576466 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010530 | GTTTTTTCTACAACC[A/T]CATAATGGGGCTGGA | 57690 |
rs143641017 | in-del | -/TA | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029508 | TATAGGGCACTTAAC[-/TA]TGAATGGAGCTTGCA | 57690 |
rs143651600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076645 | GGCTGGTTGTGATGT[C/T]AGATGACATAAATTT | 57690 |
rs143670360 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095734 | AACATCTCTTCACGT[A/C]GAAATTGCTAACCAG | 57690 |
rs143705154 | snp | A/G | 0.000397483 | 0.014092 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079400 | CCCTGTGCAGATACC[A/G]AGTGGCAATCTGGGT | 57690 |
rs143706158 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061142 | AGGTAACGATTCTAA[C/G]ACCCCATAGTACGGA | 57690 |
rs143721800 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003031 | AGTTATGGTCAGAAT[A/G]CGGGATAGTGGCATC | 57690 |
rs143792591 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108725 | GGCACCATTTCCACC[C/T]ATGGGTGAAAAAGAG | 57690 |
rs143810609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027608 | TGAAGACCCAGGACA[C/T]GCAAAGTCCCTAAGA | 57690 |
rs143859815 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078876 | GGCAGGTGGATCACA[A/T]GGTCAGGAGTTCAAG | 57690 |
rs143880127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042995 | CCCTTCAAAAAAGAG[C/T]TTATAAGTAGTAGGT | 57690 |
rs143883182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033609 | GGGACGTGGAGGTTG[C/T]GGCGAGCCGAGATCA | 57690 |
rs143924462 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061607 | TTGAATCTAGGAGTT[C/T]GAGGCTGCAGCGCAC | 57690 |
rs143948922 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015068 | GTCACATTTGCAAAC[A/T]ATCTTATATTTGAGT | 57690 |
rs143949031 | snp | C/T | 9.98004e-05 | 0.0070633 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049413 | TGGACATGAAGGAAC[C/T]GTGGCGACAGGCAAC | 57690 |
rs144035386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109177 | AAAGGCAGAAAGCAC[A/G]GTGCCCAGCAGCTAG | 57690 |
rs144048791 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093923 | GAAAAGACAGCAGGT[A/G]GTGCTTATGGAGAAA | 57690 |
rs144110841 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029080 | TTTGTTTATGCAACT[C/T]ACTCTAATATGATTT | 57690 |
rs144120739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044390 | TGTTTATTTACTGCT[G/T]CTTCTCTGTCAGATA | 57690 |
rs144122581 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082297 | GAGGGATTTAGGGTC[A/G]TTTGATTATGAGGTG | 57690 |
rs144142242 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046469 | AGGCGAGAGCCACTG[C/T]GCCTGGCCGGGAATT | 57690 |
rs144224566 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069832 | TAGGAGGAAGAAAAC[-/GT]GTGTGTGTGTATGTG | 57690 |
rs144242390 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096515 | GAGGTCCCTTGCAGC[A/G]GGGCAGCTGCAAACA | 57690 |
rs144262691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061622 | CGAGGCTGCAGCGCA[C/G]TATGATCACACTTAA | 57690 |
rs144271937 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003634 | GTTGTTATTTAGAAA[C/T]AGAAGGAAGGTGTTT | 57690 |
rs144293701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074556 | TTAGGGTGGGCCAAA[A/C]ACACACTAGTCATTA | 57690 |
rs144331944 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039716 | CAAGGGCATCCAGAG[A/C]AGACAGGGCAATAAA | 57690 |
rs144348060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100204 | TGGGGTCTAGAGGAC[A/G]GTGACCTTCTTCTCA | 57690 |
rs144357290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038935 | AGTGTGGGAAAAGGC[A/G]ACGCTGGTGTGCTGT | 57690 |
rs144374359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007665 | TCTCAAGGCCCTGAG[C/T]TGTTTGAATATAGGA | 57690 |
rs144408937 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084340 | AAAAAAAAAAAAAAA[-/G]AATGGGAACTCCAAA | 57690 |
rs144423436 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019929 | ATAAGTGAGGATCTG[-/AA]AAGAGTTTATGGCTA | 57690 |
rs144450742 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058588 | AACCAGCAGCAGTGG[A/G]GTAGTGACATCTTAC | 57690 |
rs144452942 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097508 | CTCATGCTGCTTCTT[A/G]CCCTTTGATTCCTCT | 57690 |
rs144459254 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015691 | CCGAGGTGGGCGGAT[C/T]ACCTGAGGTCAGGAG | 57690 |