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 |