SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs144486828 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003895 | GACTGTAGGAGCTGT[A/G]TCTTACTCCATATCA | 57690 |
rs144490987 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062580 | TCTATATGAAAATTA[C/T]AACTGATACAAGCTG | 57690 |
rs144501789 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021312 | GCAGAGCACAAAGGC[A/G]TCTCTGAGGGGCACA | 57690 |
rs144521968 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007604 | GCTCCAGATTGTGTG[C/T]CTATGAGGGCAGGGG | 57690 |
rs144576206 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056722 | AGCCAGCCTCGACCC[C/T]GCAAAGTGCTGGAAT | 57690 |
rs144619528 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056573 | GGTTCACGCCATTCT[C/T]GTGCCTCAGCCTCCC | 57690 |
rs144640194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025114 | ATTATTAACTAAATG[C/T]CACAGTTTACATTAG | 57690 |
rs144640471 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060177 | GATACTTTGCCATCT[A/G]ACTGTACTCTTGTAT | 57690 |
rs144662661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027033 | GTATCAAGTATAAAA[A/G]AGTGGACAACAAAGC | 57690 |
rs144697465 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065245 | TAATCCCAGCTATTC[A/G]GGAGGCTATGGTGGG | 57690 |
rs144700211 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029472 | AAATACGCTATAAAG[A/G]ATTTTTAAAAGGTAC | 57690 |
rs144718740 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031961 | AACATACACAGAGAC[A/G]GACAAATTCATTTCA | 57690 |
rs144774238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102238 | CAGGCCTCCCGGGCT[A/G]GTGGGAAGATCCAAA | 57690 |
rs144793329 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070672 | TTACTCATTGGAATA[A/C]ACCCCCTCATTTTAT | 57690 |
rs144801625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011732 | GCATATGATAGGTGT[A/G]TGTTTCATTTTTCAA | 57690 |
rs144903133 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066841 | GGCCTGCCAGACTTC[A/G]CATGATCCAGCTGAC | 57690 |
rs144998553 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023903 | TCACCTATGGTCAGA[A/G]GTTCAAGACCAGCCT | 57690 |
rs145007504 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012750 | TTTACAATGTTGGCA[A/G]CAGAGGAGCTGCTGA | 57690 |
rs145013387 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072156 | AGGCCCTCTGTATTG[G/T]GCAGGGCATTGTGTT | 57690 |
rs145014934 | snp | C/T | 0.000138262 | 0.00831337 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098562 | ATGCTCCTCGTGTTC[C/T]GATGGGGGCCTTACC | 57690 |
rs145019664 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073534 | AAGGAACAAGCAACC[C/G]TAGTTCTAGAGCTGC | 57690 |
rs145039256 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038361 | GAACTACCACAAATG[A/G]GTCCTAAGTATGTTG | 57690 |
rs145039420 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076312 | AGAGTCCTCCAGCAC[A/G]TGATCTGCCTCAGCT | 57690 |
rs145057920 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041735 | GGCTGTTGTAGCATT[C/T]ATCCTGCCCCTGAAA | 57690 |
rs145071328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040633 | AGCCGCAGTTTATTC[A/G]CCTGCAGCCAATAGG | 57690 |
rs145094833 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103130 | ACCAGAGGCTCTGTG[C/T]GACGTGCTCTGGTGA | 57690 |
rs145107506 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009081 | GAACACAATTACCTG[G/T]TACCTTAGTGAGACC | 57690 |
rs145113550 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042971 | TTTTCAGAGAGATTC[C/T]TAAGCCTACCCTTCA | 57690 |
rs145154254 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011808 | GTTCTGCATCTTCAC[C/T]AATGTGTGGTATGGT | 57690 |
rs145156660 | in-del | -/ACTACTGTACATA | 0.0383715 | 0.133092 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030123 | CTACTGTACATAATT[-/ACTACTGTACATA]ATGTATGTGCTAGAC | 57690 |
rs145176466 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084378 | ACCATTGGCATAAAA[-/C]CTTTGCTAATGAGAG | 57690 |
rs145181788 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079937 | AGAGGAAAGTGACAC[A/G]CTGTAGTATTGCTGA | 57690 |
rs145282538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087812 | TCAGCACTTGAAACC[C/T]GCAGGTCAGTAGAAG | 57690 |
rs145318852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090478 | TTACGGTAAGGACCT[A/G]TGGGGTATGTGTATG | 57690 |
rs145361071 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056069 | TGCCCAGGCTGGTCT[C/T]AAACTCCTGGCCTCA | 57690 |
rs145381889 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030180 | TTGGAGACGGAGTCT[C/T]GCTCTGTCACCCAGC | 57690 |
rs145391719 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055022 | CACCACTGCAAAGTA[C/G]AGTTCAGCACTGTAC | 57690 |
rs145429115 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089597 | TGTTCAGCCTGTCGT[C/T]GTTATTCTCAGTCTT | 57690 |
rs145430456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057714 | GTTGACCTATGCTGA[A/G]TTTATAGAATTTTCA | 57690 |
rs145468899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026697 | ATTTTATTCTGAGAG[C/T]GTTACAAGACCTCAG | 57690 |
rs145487017 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004848 | GAGCTCCAGATAGAA[C/T]TTTTTGCCTTTAGAT | 57690 |
rs145533875 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063264 | ATATATATATATATA[A/T]AAATAATATATATAT | 57690 |
rs145563322 | snp | C/T | 0.000178419 | 0.00944338 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050607 | CAACGCGCCACCTGC[C/T]GCTGTGCCAGCAAAC | 57690 |
rs145567358 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101322 | TTTCCATCTGAGACC[A/G]CTGCAGCCTGGACTT | 57690 |
rs145576197 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041585 | TAATTCCTTGTATTT[A/G]TAGTAGTTGACAGAT | 57690 |
rs145596887 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009904 | ATACTTTTTTTGAGA[C/G]AGAGGGTCTAACTCT | 57690 |
rs145654736 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041890 | AGAATGAACACATTT[A/C]CTATTTGTCAGTGTT | 57690 |
rs145657830 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101608 | CAGAGCTGAGAGCCC[C/T]AAACAGAGATTTACC | 57690 |
rs145665677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104187 | GAGACGTTGGAACCT[A/G]GAAATTAGTCATTCC | 57690 |
rs145674041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044569 | TTATGGCTGTGTCCC[C/T]AGCACAGTAGCTGCA | 57690 |
rs145674905 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010899 | AGTAGGTACATGAAC[A/G]TATAAGTTCTTGAAC | 57690 |
rs145690516 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108125 | AACCGAGCACCCCAG[C/T]GGCCCCTCAAACTAA | 57690 |
rs145697187 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013213 | TAAGGACTTTAGATC[C/T]TCTGGACCAGAGAGG | 57690 |
rs145708707 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027475 | TTTATATTCAGTTCC[A/G]TCATATGGAAACTCT | 57690 |
rs145846205 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058290 | ATGTGTGTTCTAAGG[A/G]AATGAAAGCAGATCC | 57690 |
rs145937009 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053348 | TGAAAAATAAGATTA[A/G]GTCGGGCGTGGTGGC | 57690 |
rs145937317 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019127 | GTTACAGATGACGAT[A/G/T]TTGAAGTGACTGAGC | 57690 |
rs145947853 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096075 | AAAGGCCTCCCAAAG[C/T]GCTGGGATTACATGC | 57690 |
rs145948703 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021895 | TAATTTTTTAATTAA[A/C]ATAAAACAATACCTA | 57690 |
rs145976905 | in-del | -/C | 0.103438 | 0.202533 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054772 | GACTACTGTACACTA[-/C]TATACATTACTGCAG | 57690 |
rs146017016 | snp | A/C/G/T | 0.000233819 | 0.0108104 | missense | TNRC6C | GRCh38.p7 | 17:78050531 | AGGCTTCAAACTCAG[A/C/G/T]GGGGAAGAACGATGG | 57690 |
rs146021777 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098907 | CCCATGACTCCCCTT[C/T]GCACAGGGATCTGGA | 57690 |
rs146058945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069721 | CTAAAAGGAAATTCT[A/G]TCTATGTATTGATAT | 57690 |
rs146071463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035691 | AACAGTGCAGTAAAG[C/T]TTTCTCATCACTCTG | 57690 |
rs146107573 | in-del | -/CTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006632 | TCTTTCTTCTTCTTC[-/CTT]CTTCTTCTTGAATTT | 57690 |
rs146164275 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009877 | ATTTTTAAGTCATAT[A/G]CATCTGAATTTATAC | 57690 |
rs146180081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025428 | CATGACTTGATAACT[A/C]ATTTTTTTAAATCAC | 57690 |
rs146181542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084275 | ACAGAGCAAGACTCC[A/G]TCTCAAGAAAAAAAA | 57690 |
rs146184627 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066960 | AGATGCTCATTTCAG[C/T]AGCACATGTACTAAA | 57690 |
rs146186006 | in-del | -/AC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078012 | TTAGGGATGAGGTTG[-/AC]ACACACACACACACC | 57690 |
rs146264437 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022218 | TCACATAACAGTTAT[G/T]CAAGGTGGAAAGGGA | 57690 |
rs146299744 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003818 | CTGGTAATCCCAGCA[C/T]TTTGGGAGGCCAGGG | 57690 |
rs146311710 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007081 | CTCCTGACCTCAAAT[A/G]ATTCCCCCCCACCTC | 57690 |
rs146379676 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036452 | TAATGGAAAACTTAC[C/G]TGTCCATTCCAGTAA | 57690 |
rs146381881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096844 | GAAAGGGAGAGCCAC[A/C]TTAGAAAATATGAAA | 57690 |
rs146479476 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044406 | CTTCTCTGTCAGATA[C/G]TCTGCTGAACACTGG | 57690 |
rs146490985 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046534 | CTTCTCCCTGCCTGT[A/G]GCTTGTTTTTTTAGC | 57690 |
rs146493245 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106204 | CCACCTGTTTACAGA[C/T]CTTTTTTTCTCCTTC | 57690 |
rs146549205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104268 | TAATGATCTGTTCAC[A/G]CACTTGAAGATGTAC | 57690 |
rs146590491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107036 | TCAGAGTGACTGCAT[C/T]TCATTGCCATTACAT | 57690 |
rs146600312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058831 | AGGCTCTAGCCAGAG[A/G]CACACTTTACTTTGC | 57690 |
rs146609393 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082358 | TAACATAACATCGGT[A/G]TGCAGAAGTACAGTA | 57690 |
rs146611959 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062795 | GTTGGCCCTTGAACA[C/G]TTTGGGATTAGGGTT | 57690 |
rs146615890 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004030 | TGTTAGGGAAGTGTC[C/T]CTTTCTAGCACCTTC | 57690 |
rs146720446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075789 | CAGCCCCCAGTGTTG[C/T]CATGTAATGATGTCC | 57690 |
rs146725298 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016153 | AATAATTGAGAGGCC[C/G]TATTGGCTCTCTTGA | 57690 |
rs146732573 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079088 | AGAGCAAAACTCCAT[C/T]TAAAAAAAAAAAAAG | 57690 |
rs146736559 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019547 | ATATAAAGAGTTACC[A/G]TCTACCTTTTCACCA | 57690 |
rs146762787 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109311 | AGACAGTGGGGCATC[C/T]CGAGAAGATCCTCTG | 57690 |
rs146840088 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030218 | GCAGTGGCACAGTCT[A/C]GGCTCACTGCAACCT | 57690 |
rs146843037 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090138 | CTGCGAAGTGTGTGT[A/G]TGCATGTGCATAGGT | 57690 |
rs146852201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033611 | GACGTGGAGGTTGCG[A/G]CGAGCCGAGATCACG | 57690 |
rs146854350 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093562 | CATCTTTTAAAATTT[C/T]GTGAATCAATGTGCC | 57690 |
rs146894093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020641 | TCATTTTAAATAGGC[C/T]AGTTGCATCATCTAA | 57690 |
rs146897253 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080767 | ATCTTGAAGTACTTA[C/T]AACATTCTAGCATTC | 57690 |
rs146904473 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024568 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 57690 |
rs146907574 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082675 | GCCCCTCATGCATCC[A/G]TTTATAGGCTCTCCC | 57690 |
rs146941416 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005306 | GAATGTTATATTAGC[C/T]TTCCAAACAATGCTT | 57690 |
rs146986449 | in-del | -/GTTAA | 0.107341 | 0.205301 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057141 | ACATGCTGAAAGTAT[-/GTTAA]GTTTAGTATATTGTA | 57690 |
rs146987185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091729 | AAAGTTGGATTTAAA[A/G]TAACCCATTCCATTA | 57690 |
rs146997027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094886 | TGCAGCTGCGTTTCG[A/G]AACAGGGATGTTACG | 57690 |
rs147001638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035004 | AAGCAGAATGGGAAA[A/T]TCTCTGAACCATAGG | 57690 |
rs147011273 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037820 | GATAGACTAATTCCA[A/C/G]ACTTCATCTAGAAGA | 57690 |
rs147036668 | in-del | -/AG | 0.204496 | 0.245824 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063661 | TCTGCCTTCTAAGAC[-/AG]AGATACCTCAGATCT | 57690 |
rs147048072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020377 | TCTGTTTGTAAAATA[A/G]TGTGCTAGTACTTTA | 57690 |
rs147086281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081372 | ATTGAGGGTAATTCT[C/T]GCTCTGTAATTGTTC | 57690 |
rs147106586 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048720 | TTCTTTAAGTCATTT[C/T]TTTAGTGTTTGTCAT | 57690 |
rs147116413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051907 | AGCTCCAAGTGTCCA[G/T]TGAGGACAATAAAAG | 57690 |
rs147145742 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103217 | TAAAATGTAACTGAA[A/G]CATCCAAGTTTTTAG | 57690 |
rs147156112 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105419 | CCTTGTTTCATTACT[C/T]TTTCATGTCATTTTT | 57690 |
rs147191175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057575 | CGTGCTGCCCACTGG[C/T]TTGAATGCCTGCGCA | 57690 |
rs147200952 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061326 | GATAAACACTTAACA[A/G]TGGAGATTATTTTAA | 57690 |
rs147204884 | snp | C/G | 0.0228947 | 0.104514 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003123 | AAGCACCCTGGTGAT[C/G]AGGTGGGGGAAACTA | 57690 |
rs147249220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057974 | TTCCTAAACTGGATT[G/T]TCTGGACCTGGTTCA | 57690 |
rs147296268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015282 | CATCTATTCAATAAC[A/G]TCCTGTTGACAGAGG | 57690 |
rs147298881 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073867 | TTCATACTCAAAACA[A/G]TGCCGTCCACCACAC | 57690 |
rs147306142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018060 | TGTCTCTTCTACTAT[A/G]TGATAAACTATAAAG | 57690 |
rs147356590 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074926 | ACGGAAGGGTGCCTG[A/G]GGCCAACCCCCATCC | 57690 |
rs147366829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078147 | CACCAGCGCCCGACT[A/G]TGTGATCCTGGCGAT | 57690 |
rs147403003 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029415 | CAGTTGCAACACAAT[A/G]GTAAGTATTTATGTT | 57690 |
rs147462357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089124 | AGGCATGCATCACCA[C/T]GCCTGGCTAATTTTT | 57690 |
rs147472090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092706 | ATCACTACACTCCAG[C/T]CTGGGCCACAGAGTG | 57690 |
rs147508282 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042722 | GTGATGATGGTGGAG[A/G]TAACAATGATGGTAG | 57690 |
rs147519048 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045619 | ATGCATGTATGGTTT[C/T]GTTTGCCCAGGAAGC | 57690 |
rs147556431 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040795 | GTTTAGTGTCAGCTG[C/T]AATTAGATAATCAAA | 57690 |
rs147557885 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101152 | AGTCACCTCTTGAAG[G/T]CTTTGCTGCTTAGAA | 57690 |
rs147566485 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009596 | TTTTGCTCTTGTTGC[C/T]CAGGCTGGAATGCAG | 57690 |
rs147576177 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011878 | GTATCTCATTACACT[C/T]TTAATTGGCATTAAC | 57690 |
rs147630758 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038227 | TAAAATCTGAGAGGA[C/T]ATGTTTACAGTGTAA | 57690 |
rs147653488 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098691 | CACCCTAGATGTCCA[C/T]CCAGGGCAGTAGCTG | 57690 |
rs147661011 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055344 | TCCCATTGGAGATCC[A/G]ATAACAGGAAGTACA | 57690 |
rs147671027 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024169 | AAAATAATTGTTAGT[A/G]TGCTAATTGTAATTT | 57690 |
rs147680671 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026962 | GAGAGATTGAAATAC[C/T]CAGAAGGGCGAGGCG | 57690 |
rs147692121 | in-del | -/AAATACTC | 0.241627 | 0.24986 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097289 | CACCCCAGTCAGAAG[-/AAATACTC]AAATTTTTATGGCAA | 57690 |
rs147755216 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051978 | GGTCCAGAGTAGAGA[C/G]ATTTTAAGGTGGCAA | 57690 |
rs147766484 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071781 | TTTCATTAGTGTATA[C/G]AGTATATTGACAGAG | 57690 |
rs147776201 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037526 | GTGGAGGTGATATGA[A/G]CTGAGTTTCAAGTTA | 57690 |
rs147785803 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039821 | TGTGGGCATTTCAGC[C/T]GTCAAAGGGCTGTCC | 57690 |
rs147835038 | in-del | -/TTAT | 0.0240643 | 0.107019 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021560 | GAGACATGGAATAGG[-/TTAT]TTATTTTTTTATTTT | 57690 |
rs147857432 | in-del | -/CCCCCCC | | | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78051352 | ATACCACCACCACCA[-/CCCCCCC]CCACCACTACCACGA | 57690 |
rs147861646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067659 | GGTAGATTACAATGC[A/T]TCATTTGTCCCACGA | 57690 |
rs147871187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048447 | CTTAAAGAGAACTAC[A/G]AGTTTTATTCAAAAC | 57690 |
rs147882211 | snp | C/T | 0.0483635 | 0.147793 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051411 | GCCCCCGCACCAGGC[C/T]GGTACTCAGCTGAAT | 57690 |
rs147968283 | snp | A/G/T | 0.078151 | 0.181571 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082699 | CTCTCCCCAAGGGTC[A/G/T]CATTCCATTCCCAGA | 57690 |
rs147986718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030293 | TAGCTGGGATTACCC[A/G]TACCTGCCACCACAC | 57690 |
rs148014653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081411 | GTTTGTGCACTGAGT[C/T]GATAGTGCACAATTA | 57690 |
rs148018973 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021485 | ATGTTCCTGTTTCTT[C/G]TTGATAAATAGCATC | 57690 |
rs148027702 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010821 | AAAAAAAATATTAAG[A/G]TGAGACATTTTAAAA | 57690 |
rs148036511 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057169 | TATTGTACAACATAT[A/G]GGGTTATTTGTTCAT | 57690 |
rs148083261 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042171 | TAGATTTTTATAGAC[A/C]CCTATTTATAGACTG | 57690 |
rs148167459 | in-del | -/T | 0.0659589 | 0.169201 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029773 | CTTTTCTGTGTTTAA[-/T]TTTTTTTTTAACTTT | 57690 |
rs148179848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076909 | TGCCATCCTTCCTCC[A/G]TGCTCCTACCTGAGG | 57690 |
rs148194115 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060354 | TTAAGTTTAAAGGCC[A/G]TTGGTATGAGTAAAA | 57690 |
rs148195947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084113 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57690 |
rs148231811 | snp | C/T | 0.000960201 | 0.0218901 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049581 | GAATGTGTCTTTCAG[C/T]GCACAACCTCAGAAC | 57690 |
rs148242434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038269 | TAAATATCTCAAAAA[C/T]ACCAAGTGTTCCGAC | 57690 |
rs148249731 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088636 | TTTTTCTCTCTCTTT[G/T]TTTTTTTGGCTGGAG | 57690 |
rs148337859 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101478 | TTCCAAAGTTGCTTC[C/T]GTGCCAAGACCAGCT | 57690 |
rs148383822 | snp | A/C | 0.000227505 | 0.0106631 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104453 | CAGGACTTGGGGTGG[A/C]CCTGTTCACGTGCCC | 57690 |
rs148393067 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015702 | GGATCACCTGAGGTC[A/C]GGAGTTCCAGACCAG | 57690 |
rs148395543 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075071 | GAGGCCTTAGCTGGT[G/T]CCTATCTTGTGCTCA | 57690 |
rs148409613 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013718 | AGGTATCATTGAATC[-/T]TGAAGGGTGAGCAGG | 57690 |
rs148491283 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105783 | ATTGGTCAAACGGTT[A/G]TTATTATTAGCTTCT | 57690 |
rs148493851 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025522 | CTTCCAGTTTTTGAC[A/G]ATTATGAATAAAGCT | 57690 |
rs148508842 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032321 | TCATCCTAAGCCCTG[C/G]TTCTTGTTGCTTCCT | 57690 |
rs148541090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024018 | GGGAGGCTGAGGCAG[C/G]AGAATCACTTGAACC | 57690 |
rs148552135 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070882 | GCACATATATACCAA[C/T]CTGCAAATGTACCTT | 57690 |
rs148604330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043129 | GAGAGCAGCTGAAGT[A/G]TGGAAAAAAAGGAAA | 57690 |
rs148710192 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096554 | GGTTGGACACTGCAC[A/G]TGTCCAGGAGGTGCC | 57690 |
rs148718404 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003659 | GTGTTTTCAAGAAAA[C/T]AGAGAACTGAAAGGT | 57690 |
rs148720232 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061984 | GATAAACAAATTCTA[A/G]GTGAGTTCATTATTT | 57690 |
rs148751628 | snp | C/T | 9.68758e-05 | 0.00695906 | missense | TNRC6C | GRCh38.p7 | 17:78051379 | ACGAGCAACACCACA[C/T]ACAGGGTCGAGACGC | 57690 |
rs148757431 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100437 | AGAGTCTCAACACCA[A/C/T]GTGGAAGCTGCCAAG | 57690 |
rs148761747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039193 | TAGATAGCATTAGTC[C/T]TCCAGTGACCAGCAA | 57690 |
rs148770822 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007706 | CAATTTGAGAGAGTC[C/T]GAGAGTTGGATACTC | 57690 |
rs148804537 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086532 | ACAAATCCAGCAGCA[A/G]ATGTTACAGGCCCAG | 57690 |
rs148812380 | snp | C/G/T | 0.00296275 | 0.0383773 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098555 | AAGCTCCATGCTCCT[C/G/T]GTGTTCCGATGGGGG | 57690 |
rs148826074 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005006 | GTGTACATTCTACAC[A/T]TTATTCCTAAAGAGT | 57690 |
rs148849683 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063333 | ATTCATTAGGTGGAA[C/T]TGGATCATCATAAAG | 57690 |
rs148863696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041660 | GTACTTTCTCCCTGA[A/G]ATCTTTACACCCAGT | 57690 |
rs148866021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101378 | TTGTCAAAGCCATTT[C/T]ACAAGTCTCTAGGAA | 57690 |
rs148867628 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019662 | TTTAAAATTATATAT[G/T]TAGTTATTAAATGGT | 57690 |
rs149005409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058299 | CTAAGGGAATGAAAG[C/T]AGATCCTAAAAATAC | 57690 |
rs149014876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027510 | AGAAAAAAAACAGAG[A/G]AATACTTGTAAAGCA | 57690 |
rs149056090 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034486 | CCCCCACTTTACTTC[C/T]AGTTCATTGTCCCCC | 57690 |
rs149064283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083866 | CTATAATTGCCATGT[C/T]ATTGTATACCTAGAT | 57690 |
rs149109595 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038250 | CAGTGTAAATAGCAA[A/G]AGATAAATATCTCAA | 57690 |
rs149126601 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044852 | CTTGAAAGGAAGACT[A/G]TTACAATGAATGTAT | 57690 |
rs149217298 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090057 | AACGAAAAGAACCCA[C/G]ACAGCAGAGATTGCA | 57690 |
rs149222597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080660 | CAATGGTATTGATAA[C/G]ATCTTTGCTGCGTGG | 57690 |
rs149227172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055389 | TGGTAACATAGTCTT[A/G]TATCAGCATCATCAG | 57690 |
rs149257424 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105676 | CGTGCTCCTGCACGG[C/T]GTGCAGTTTTCTGTG | 57690 |
rs149276041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052564 | AGAAGGTCTGCATGC[A/G]GGGGCCACTGGAGTT | 57690 |
rs149318743 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091662 | GGCTTATTAATCGAT[C/T]GTCCTGTTGTATAGC | 57690 |
rs149371465 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065206 | AAAATTGAAAAATTA[A/G]CCAGGCATGGTGGCA | 57690 |
rs149381661 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031826 | AACACAGCATCATCC[C/T]AGTAAGCTCCAACCA | 57690 |
rs149392121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021311 | AGCAGAGCACAAAGG[C/T]GTCTCTGAGGGGCAC | 57690 |
rs149415937 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102228 | TGGGAAAACACAGGC[C/T]TCCCGGGCTGGTGGG | 57690 |
rs149425928 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070196 | AATAATCCAGTTAAT[C/G]ATGGGACCAAAAATA | 57690 |
rs149430326 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011611 | ATCTGCGTTTTTCCA[C/G]TTTTGAGCTATTGAG | 57690 |
rs149459201 | in-del | -/TGG | 0.0652144 | 0.168387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052752 | TCCTCGTAGACTTCT[-/TGG]TGGTTCACTTGTGTA | 57690 |
rs149469626 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078736 | TTGGGAGGCTGAGGT[A/G]AGTGGATCCCCTGAG | 57690 |
rs149540024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028673 | ACAATGTAAAGGGAA[A/G]CAGTACCGTATCATG | 57690 |
rs149573552 | in-del | -/AA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086359 | AAAAAAAAAAAAAAA[-/AA]CAGTATGTGTCAGCC | 57690 |
rs149582797 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035575 | CCTGACAGGCTGAGG[A/C/G]AGAAGGATCGCTTGA | 57690 |
rs149584323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096448 | AAAAGTGAAGACCTG[C/G]AGATTACCCATAAAT | 57690 |
rs149592772 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003214 | AAGCAAAACCCACTG[C/G/T]GAAGGAAATCCATCC | 57690 |
rs149625642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073748 | ATAACCTTGTTTTAT[A/G]TGTTTTTCTGTTTCA | 57690 |
rs149676375 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046228 | ACTGTGTTGCCCAGG[C/G]TGGAGTGCAGTGGCA | 57690 |
rs149684659 | snp | A/G/T | 5.01017e-05 | 0.00500488 | missense | TNRC6C | GRCh38.p7 | 17:78098399 | ACCTCCCACACGCAA[A/G/T]CCTCTCTGTCTCATG | 57690 |
rs149686390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015673 | CCCAGCCACTTTGGG[A/G]GGCCGAGGTGGGCGG | 57690 |
rs149698004 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004091 | AATTCTGACTTAAGA[C/T]TTGGAGCAGCTAGTG | 57690 |
rs149799010 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054828 | TGCAGACTACTGTAC[A/G]CTACCATACACCACT | 57690 |
rs149842936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093552 | CAGGACAAAACATCT[C/T]TTAAAATTTCGTGAA | 57690 |
rs149853250 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058269 | GAAAGTGCAAACATA[A/G]CATTTATGTGTGTTC | 57690 |
rs149868276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018745 | TTGTTCCTTGATACA[A/G]CCCCAGCCTAGAGGA | 57690 |
rs149895145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066688 | ACTTTGTATTTTAAG[A/G]TAGGAGGAAAAAACA | 57690 |
rs149905249 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033970 | AGTTACTAATGCACA[A/G]ACTCTCCGTTTTTCT | 57690 |
rs149939255 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104087 | CTACACAGGGCCCAG[C/T]AGTGGTCCTCACAGC | 57690 |
rs149941692 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023317 | TAGTAGCTAGCCATC[C/G]AGTGTCAGTTATTTA | 57690 |
rs149948650 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072067 | TATCTTTCAGTTACC[A/G]TAGATGCTTCTAAAA | 57690 |
rs150067482 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030077 | AGTAAATACATAAAC[C/T]AGTAATATAGTTATT | 57690 |
rs150085990 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091258 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAATGAGC | 57690 |
rs150157509 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041371 | GGTTTCTCTCTGCTG[A/G]GCTGGCACGGGCAGG | 57690 |
rs150168813 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030511 | GTTGTGACATTGCAA[C/T]GGCTGTGTCACCAGA | 57690 |
rs150201841 | snp | C/T | 0.0221141 | 0.102801 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108035 | TCCCTTCCTAGGACA[C/T]TGGCCGTGGCCTTCA | 57690 |
rs150205733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047919 | CAAATAATTGTTAAA[A/G]TCATAGGAAATAAAA | 57690 |
rs150242687 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087372 | ATCCTCCCACCTCAG[A/C]CTCTTAAAGTGCTGG | 57690 |
rs150252046 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052216 | GTGAATACTAGCCCA[C/G]AGTGGAGGAGGGCTG | 57690 |
rs150348224 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064189 | AACCACTTGGTTCCC[A/G]GGTTCAAGAGATTCT | 57690 |
rs150371427 | snp | A/C/T | 0.00358891 | 0.0422285 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012601 | ATGCAATAAAATGTT[A/C/T]TGGGCATTGTAACTG | 57690 |
rs150404829 | in-del | -/T | 0.0569829 | 0.158885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075669 | TGGAAGTGGTGGGGC[-/T]TTGGGCACCCATCTC | 57690 |
rs150410384 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079936 | GAGAGGAAAGTGACA[A/C/T]GCTGTAGTATTGCTG | 57690 |
rs150421962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068742 | GAGGTTGCAGTTGCA[A/G]TGAGCCAAGATCGCC | 57690 |
rs150431869 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035112 | TCTCATGATCTCTAA[G/T]GTCCTTTCCCTTAAA | 57690 |
rs150459940 | snp | C/T | 0.00307502 | 0.0390904 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104874 | CAGCACCAGGAGAGC[C/T]GACCCCTCCCGGGAC | 57690 |
rs150469302 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024750 | TCACCACCACTAGTT[G/T]CCCATATTTGTGTGG | 57690 |
rs150513072 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081688 | GTGGCCTTGAAATTG[C/T]ACACACCACTTCCAG | 57690 |
rs150523665 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046002 | CACAATTCAAAAATT[A/G]TAGTGTTGTGTCACT | 57690 |
rs150566725 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084912 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 57690 |
rs150571137 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025738 | ATATAATGGATGTTC[A/T]TTCTGTATAAAGGTA | 57690 |
rs150608960 | snp | C/G | 0.000106451 | 0.0072948 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093165 | AACAGCAGCAGGTCA[C/G]AATGTGCTCCAAGCC | 57690 |
rs150613984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033507 | AAACCCAGTCTGTAC[C/T]AAAAATACAAAATTA | 57690 |
rs150643900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006663 | TTCTGTCTGGTTTAG[C/T]ACCAGCTATATTCTT | 57690 |
rs150681948 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102129 | GCACTGATTCCACAC[C/T]GGGTCTGGGGACAGG | 57690 |
rs150686283 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042325 | GCACTAGATTATATT[C/T]TGAAAACTCAGATTT | 57690 |
rs150695788 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011490 | TTTTGAAATTCATCC[A/G]TGCTGTAGTGTGTAT | 57690 |
rs150727299 | snp | A/G | 0.00096485 | 0.021943 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050037 | TGGTAATATCCATTC[A/G]GGAGCTTGGGGCCAC | 57690 |
rs150736887 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018488 | GCACAGAATAGGAAC[C/T]CATTAAATATTTTCT | 57690 |
rs150755282 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100458 | AGCTGCCAAGGCTTG[A/G]AGATTGCTCCCTCTG | 57690 |
rs150771315 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089009 | GTCTTGCTCTGTTGC[C/G]CAGGCTGGAGTGCGA | 57690 |
rs150780858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054328 | ACGCACACCACTGCA[C/G]ACTACTGCACACTAC | 57690 |
rs150824625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062290 | AGAGCTTGTAATTTA[A/G]AATGATTTTTAGGTT | 57690 |
rs150834322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029547 | AAGTTGCTCTGAGGA[A/G]TCAGTGAGTGGTGAG | 57690 |
rs150926587 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063637 | ACTCTGATCCATAAT[G/T]CAACTCTCTTCTGCC | 57690 |
rs150999797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075461 | TGTCGTATTTCATAA[A/G]ATGTTACTGAGAATG | 57690 |
rs151052535 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047299 | CAAATTGTCATAAAC[C/T]AGGGTTATAGAGCCA | 57690 |
rs151089943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087198 | AGGAGGACTGGCCAG[C/T]GCTGAAACCATAGCC | 57690 |
rs151114115 | in-del | -/CATTTCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061819 | AAAATACTTACTAGA[-/CATTTCT]CCTGCCTTTAAGAGG | 57690 |
rs151133458 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094683 | GACCTCAAGTGATCC[A/G]CCTGCTTTGGCCTCC | 57690 |
rs151141821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012460 | ATGAGTTTACCTGTG[A/T]AACAAACCTTCATAT | 57690 |
rs151232767 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103916 | TTAAAGACCCCATCT[C/T]CAAACGTAGTCACAT | 57690 |
rs151263474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020085 | CTTAAGTCAGAAGGT[A/T]TATCACTGCATAATA | 57690 |
rs151279860 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069521 | CTGAGTAGCTGGGTC[-/T]TACAGGTGCATGCCA | 57690 |
rs151284550 | snp | A/G | 6.64584e-05 | 0.0057641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079571 | CAAGCAGGACTGAGC[A/G]ACAGGATATAGATGC | 57690 |
rs151294655 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066352 | TTGTGGTTTTTTTTG[G/T]TTTTTTTTGTTTTTT | 57690 |
rs151297630 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008535 | TAGTTGATTCACTTT[A/G]GCTTTCATCAGTTTC | 57690 |
rs151306505 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055577 | GACCATTGTCCTGTA[C/T]GCAGTCAGTTGACCA | 57690 |
rs151316369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024698 | GTTTACAAAACAATC[A/G]AGCTGAAAGTATAAA | 57690 |
rs180796330 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056825 | TTCATGCTGAGAAAG[G/T]CATTCTTGTTCAGTT | 57690 |
rs180802352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011171 | ACCAGTTTCTTTTCT[A/G]TGTTTTTTTAAAAAC | 57690 |
rs180802504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076341 | CTGCAGCTGTGGGGT[A/G]GCCCAGGGTGAGGCT | 57690 |
rs180823063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084812 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 57690 |
rs180824052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028777 | ATAAACTCATTTTGT[A/G]CATAGCTGTTTCTCA | 57690 |
rs180826028 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047085 | GCTGTCTTAGTCAAG[A/C]GGCAGCCTGCCTTAT | 57690 |
rs180830990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036579 | GTAAGAATAGATAAA[A/G]TGTATATTTATATAC | 57690 |
rs180849662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069224 | TAAAAAAAAAATCAG[C/T]CAGAAACCCAGTAGA | 57690 |
rs180853406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094262 | AAGTAATGTCTTATC[A/G]TAGAAGTGCCATCTC | 57690 |
rs181040679 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068381 | TTAATTTCTAATACA[A/G]TAAATAGCAATAGAC | 57690 |
rs181052976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031888 | TGATCTGAAAACTTT[A/G]CTATTTTCAACTTTG | 57690 |
rs181071665 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014073 | AGGATTCTGCACTTT[G/T]GGAGAGAAAATACCT | 57690 |
rs181091764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084019 | CCGGGCACGGTGGCT[C/T]ATGCCTATAATCCCA | 57690 |
rs181099354 | snp | C/T | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78104601 | GGCAGTCCAGCAGCG[C/T]GTCCAGCCAGCCGCG | 57690 |
rs181103030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058907 | CTGAAACAATTATCA[C/T]CTTATAAAATATAAA | 57690 |
rs181107439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095023 | GCTTGTCACACCTGG[C/T]GGGGCACCAGGGTTG | 57690 |
rs181110661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019171 | AGCCAACTAAAATGG[C/T]TAGGAAAGAAGCAGA | 57690 |
rs181111378 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037404 | TGGAATAACCAATAA[G/T]TAAGTCAGCCACTTC | 57690 |
rs181132395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077634 | TGCACAGTGGTCTTC[A/G]GCTGCCGGATGCATC | 57690 |
rs181321289 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014305 | TCTTTGCCTTTAATG[A/G/T]TTTGTCCAGTGTGTT | 57690 |
rs181327902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062846 | CTTCCCAAAAACTTA[A/G]CTACTTGACCAGAAG | 57690 |
rs181339522 | snp | C/T | 0.000185822 | 0.00963724 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78097812 | GCCACTCAGTGCCTC[C/T]GGCTACAGTAGCTCT | 57690 |
rs181341024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052232 | AGTGGAGGAGGGCTG[A/G]CTAGGAGCAGCAGCA | 57690 |
rs181342734 | snp | A/G | 8.85152e-05 | 0.00665205 | missense | TNRC6C | GRCh38.p7 | 17:78073091 | AATCTTGATCAGGCC[A/G]TGAGTAAGTCATACA | 57690 |
rs181343125 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023417 | TTCCTTCTCCTGCTC[C/T]TCCTCCTCCTCCTCT | 57690 |
rs181348648 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032602 | GTAACAACTAATAAT[C/T]GGTGCTGTTTCTGGA | 57690 |
rs181370957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090480 | ACGGTAAGGACCTAT[A/G]GGGTATGTGTATGTG | 57690 |
rs181395452 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003318 | AGGCTTTCAGATCAG[A/C]GAGTATCTAAGGGAA | 57690 |
rs181425244 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041174 | GGAACAAACACGGAA[C/T]AAATAGTGGCTGCTT | 57690 |
rs181477777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072413 | GCAGCTCTGCACTCC[A/G]ACAGTGACTGACATA | 57690 |
rs181484880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041823 | TGTTGAAAGCATTGC[A/G]AACTAGTTTTTATAA | 57690 |
rs181488801 | snp | C/T | 1.82121e-05 | 0.00301757 | missense | TNRC6C | GRCh38.p7 | 17:78050662 | AAAGCGCCAAGTGGC[C/T]CGGGGGTTTGGGGGG | 57690 |
rs181490404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024200 | TAAAACACATTGAGT[A/G]GTTCTAAGTTTACCA | 57690 |
rs181491959 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003673 | ATAGAGAACTGAAAG[A/G]TATGAGCTGAAAGCA | 57690 |
rs181655182 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013704 | GGCAGGAGTTGTGGA[A/G]GGTATCATTGAATCT | 57690 |
rs181690797 | snp | C/T | 0.039522 | 0.134904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027931 | TTTTTTGAGATGGAG[C/T]CTCGCCCAGGCTGGA | 57690 |
rs181693772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046172 | GGCCTCTTTCTTACC[A/G]ATTTTTAGGATTCTT | 57690 |
rs181703355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081406 | CCCAGGTTTGTGCAC[C/T]GAGTTGATAGTGCAC | 57690 |
rs181718188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008904 | ATATATTTATATGGA[C/T]TCTCCACTGCTCCCC | 57690 |
rs181737608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031255 | AGGGTGAGAACTGCT[A/G]CTCCAGTCTTAATGT | 57690 |
rs181743043 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081848 | CTCACTGTTTCTTCT[G/T]TATCTCCCTGTTACC | 57690 |
rs181773802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100040 | TGACTTCATATCTCG[C/T]ATCTGGGTCATGCTT | 57690 |
rs181790775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097985 | GGGAGGCCGTGTGGC[A/G]TGATGAAGGATGGGT | 57690 |
rs181812922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064165 | ATAACTTAGGACTTC[A/G]TAAAACTTAACCACT | 57690 |
rs181919122 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072522 | ATGGCAGGTGTCCTT[C/G]TCTGTGGCCCTGCTG | 57690 |
rs181949234 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084219 | AACCTGGAAGGCGGA[A/G]GTTGCAGTGAGCCTC | 57690 |
rs181950230 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017030 | ACTCCCTCTCAGGAG[A/G]AGTGTATGGAACTGA | 57690 |
rs181955230 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046477 | GCCACTGCGCCTGGC[C/T]GGGAATTCTTTAAGC | 57690 |
rs181956373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068951 | ATTTCAAGTAGGTCA[C/T]AAACTTAAATATTAA | 57690 |
rs181973116 | snp | A/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106776 | CTTCAAGTATGTTTT[A/T]AAAAATATATATATG | 57690 |
rs182169990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020356 | ACATGCTTTGTGGCA[A/T]TTTTTTCTGTTTGTA | 57690 |
rs182171630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038661 | TCCAGCCTGGGCGAC[A/T]GAGCGAGACTCCGTG | 57690 |
rs182184185 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028486 | CCTGAGTCAGGAAGT[A/G]GGGAGAGTAGACAGT | 57690 |
rs182184891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078950 | ACAAAAAATTTAGCC[A/G]GGTATGGTGGCAGGC | 57690 |
rs182191199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096199 | GTTCCCACTTACAAA[C/T]GGGAGCCCAACACCG | 57690 |
rs182198107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059585 | GGACACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57690 |
rs182215751 | snp | G/T | 0.000798403 | 0.0199641 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051396 | CAGGGTCGAGACGCC[G/T]CCCCCGCACCAGGCC | 57690 |
rs182229147 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090022 | TTGCCACCTTACCTG[C/G]CTAGATCTGTACAAG | 57690 |
rs182449955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009842 | ACAGGCGTGAGCCAC[C/T]GCCCCTGGCCTGAAT | 57690 |
rs182503633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011950 | TCATCTTGGTGAAGC[A/G]TCTTTTAAAGTCTTT | 57690 |
rs182528658 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070484 | CCTCCTGGCTCTTCT[G/T]TGGTGCCGAGCCCTC | 57690 |
rs182534722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047708 | GAAAATATTTTATTG[C/T]AGTTTATTTGTATAT | 57690 |
rs182536785 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029256 | TTGACAGAGAGATAC[A/G]TTCTGAAAAATGCAC | 57690 |
rs182555905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085248 | TTTTTATTGACCTCT[A/G]TAGTGTGAAAGACAT | 57690 |
rs182647023 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091968 | GAAAATCAAATATAC[A/C]GTATGTATGGGAACT | 57690 |
rs182656947 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054977 | CTGCGGACTACTGTA[C/T]GCTACCATACACCAC | 57690 |
rs182660348 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074957 | CCTTGCCGTGAATCC[C/T]TGGCAGCCCCTTGTT | 57690 |
rs182826760 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079145 | TCCCAGCTACTCGGG[A/T]GGCTGAGGCAGGAGA | 57690 |
rs182834539 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039793 | CTACAACAAGCCCGA[G/T]AGGAGGAGGGCCTGT | 57690 |
rs182840772 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108437 | CCCTCAGCTCTGCGC[C/G]GCCGAGCCTCAGCAA | 57690 |
rs182861357 | snp | A/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109107 | ATGAGCCAGGTGCCC[A/T]GCCTTTGTTGTTGTT | 57690 |
rs182996083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025760 | ATAAAGGTAAAGAAC[C/T]TTAAAATCTTAAGTA | 57690 |
rs183002632 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007029 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 57690 |
rs183020795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066745 | ACTTTGTAGCTCCAT[C/T]TGCCTAAGGCCTCCA | 57690 |
rs183033313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073891 | ACCACACTTCCTAGT[C/T]ATCATCTCATGAATC | 57690 |
rs183037741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044778 | CCCACAAAGCCTAAA[A/G]CATTTTGGCTATTAG | 57690 |
rs183039121 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090947 | TGATGAGTTTCCGTA[A/G]GATATCCCAAAACAA | 57690 |
rs183066550 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043680 | TCTTATTTATTCTTT[C/G]TGATTATTTTTTGTA | 57690 |
rs183068149 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024435 | GCAGTGGCCCGATCT[C/T]GGCTCACTGCAAGCT | 57690 |
rs183081585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024985 | TTTTAATAGAGACGG[A/G]GTTTCACCATGTTAG | 57690 |
rs183100777 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065084 | CCAAGCACAGTGCCT[A/C]ACACCTATAATCCCA | 57690 |
rs183102039 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015269 | TCATAGGACATATCA[C/T]CTATTCAATAACGTC | 57690 |
rs183107747 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021646 | GCAGTCTCGGCTCAC[G/T]GCAACCTCTGCCTCC | 57690 |
rs183110401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065764 | ACTTGAAAAAATTTT[A/T]AAAAGGTACATTTTC | 57690 |
rs183141407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060794 | CATCACACTTATAAA[C/G]CTATGTAAGTGGCAT | 57690 |
rs183145665 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101245 | GCAGGGGCAAAATGC[C/T]GCCAGTCTCTTTGCT | 57690 |
rs183162324 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096514 | AGAGGTCCCTTGCAG[C/G]AGGGCAGCTGCAAAC | 57690 |
rs183349780 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038226 | ATAAAATCTGAGAGG[A/G]CATGTTTACAGTGTA | 57690 |
rs183360242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005841 | TACAAAGACTTAATA[C/T]GATTATTTGTCAATT | 57690 |
rs183361266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019829 | CCTTATCTGTGAGGT[A/T]TGGCCCTAGAGTCAG | 57690 |
rs183375239 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082188 | GTGAAAGCTGGGTCC[A/G]GGGGGTCACCGCCTT | 57690 |
rs183379136 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052516 | TATACGTAGTGTTGG[A/G]CAGTGATGGTGCAGG | 57690 |
rs183382260 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044596 | TGCATATAGGAGGCA[C/T]TCAATAATAGTTATT | 57690 |
rs183403698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014419 | CTCAGCTTTAACATA[C/T]GCTCTTAGCGGCATT | 57690 |
rs183442449 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082519 | CTGGTTGCAAACAAT[C/G]AATAGAAACAGGACA | 57690 |
rs183500406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070773 | CAAGGGAGCGCTTAG[A/G]ATTATTGGATAGTAA | 57690 |
rs183515545 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108892 | GTCTCCCACGCTGGA[A/G]TGCAGTGATGTAATC | 57690 |
rs183526250 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087281 | TTAATTTTAAAAAAA[A/T]TTTTTAATTATTTTT | 57690 |
rs183621278 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012355 | GAGGGTGGAGGGTGG[A/G]AGGAGGGAGAGGAGC | 57690 |
rs183638271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033167 | TTCTGGTTGTATCTG[A/G]TTGTGATGTGATTGG | 57690 |
rs183666668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033727 | AAACACACACACATA[C/T]TGAAGAACATAAATC | 57690 |
rs183701732 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102112 | ACCAGAAGAACCTGG[A/G]AGCACTGATTCCACA | 57690 |
rs183714038 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074612 | ACAGTGTCTGTTTTG[C/G]ACAGTATTGTATCCC | 57690 |
rs183782972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062424 | GTAATTGATATTGTA[A/G]TATCCATGTTGAGGC | 57690 |
rs183790094 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040924 | TTGCGGCCGCGGGCG[C/T]CCGCGGGTGGCCCGG | 57690 |
rs183834809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080173 | AAAATGTTGCCGGGC[A/G]CGGCGGCTCACGCCT | 57690 |
rs183839095 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097661 | AGGGAGAGGTTGATT[C/G/T]CTGATGGTTCTCACA | 57690 |
rs183847902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030861 | CCCAGCACTTTAGGA[A/G]GCTGAGGCGAGCGGA | 57690 |
rs183859907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012666 | AGCATTTCATGGCCA[G/T]TGGCGGATAGGGAGC | 57690 |
rs183873614 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088930 | GTCTTCTTAACCTAT[A/G]TTTGGAGGATAAAGT | 57690 |
rs183883077 | snp | A/G | 0.00033631 | 0.0129631 | missense | TNRC6C | GRCh38.p7 | 17:78050020 | AGTGGCAACAATGGC[A/G]TTGGTAATATCCATT | 57690 |
rs183888437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053132 | ACACTGAGGCTTTTG[A/G]TCAGTAGCCACTGAG | 57690 |
rs183889882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071997 | GATGTCGCCCATATT[C/T]GCCATGTATTCGCTT | 57690 |
rs183906181 | snp | C/T | 0.000716242 | 0.0189105 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091412 | ATTTAGAGGAGCAGG[C/T]GAATCCTAACCGCAT | 57690 |
rs183999042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095664 | TCTGGTACCTCTCTT[C/G]GTTGTGTTTAGGGAT | 57690 |
rs184012642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059408 | TGGACTTCAGCAAGG[A/G]CTGGGGAGTTGGGAG | 57690 |
rs184093977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034497 | CTTCCAGTTCATTGT[C/T]CCCCCGCACCCGTGA | 57690 |
rs184098009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016213 | CCAGGGGTCAGGAAG[C/T]GGCACTAACACTGTC | 57690 |
rs184123100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012157 | ATAGAATCACATTTT[A/G]TCTAGCTTTTAGCAT | 57690 |
rs184154978 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048032 | ATCTCCAAAGAAAAG[C/G]CTCTAAAGAAATAGA | 57690 |
rs184168995 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078794 | ACATGGCAAAACCCC[G/T]TCTCTACTAAAAACA | 57690 |
rs184336253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048355 | GGTTCTGTTATGATT[A/C]TGCAATGCAATTTAC | 57690 |
rs184340837 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028147 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 57690 |
rs184341019 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046389 | CACCATGTTGGCCAG[A/G]CTGGTCTCGAACTCC | 57690 |
rs184350262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087679 | GTATTCAGATTTACA[C/T]TAAAAGCACTTCTTA | 57690 |
rs184363284 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084140 | AATACAAAAATTAGC[C/T]GGGCATGATGGCGCA | 57690 |
rs184371485 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022572 | GTAGCTGGGTCAGTC[A/G]TCTCAGCCATATCAT | 57690 |
rs184377636 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068529 | CAGGGCACAGTGGCT[C/G]ACACCTGTAATCCCG | 57690 |
rs184457481 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002296 | CCCTGAAGAGTAACA[C/G]ATTCTTCTCAGGGCC | 57690 |
rs184490567 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071814 | CACAAAAGAAAACTT[A/G]ATGTAAAGTACTAAG | 57690 |
rs184668266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081226 | CTCCCAAAGGCCTCC[A/G]CTCTTAACACCACCA | 57690 |
rs184764133 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017783 | TCAGCCCCCGAAGGC[A/G]AGAAGCTCTTTTCCA | 57690 |
rs184768624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045168 | GCAGTAGGGGGCATG[A/G]GAAGAGACCTGTTGG | 57690 |
rs184768748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067097 | ACTGTAATCCCAACA[C/T]TTTGGGATGCCGAGG | 57690 |
rs184787762 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102607 | CCCGCTTGGCCCCCA[A/G]TGCAGATGAGGCTGT | 57690 |
rs184796896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036281 | GAAAGTGAAGTATTC[G/T]TGGAAGGAATTGACG | 57690 |
rs184799153 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097852 | ATTGCATCCGCACCT[A/G]GTGTTGCAGGTACGC | 57690 |
rs184799690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082984 | GAATTTTGAAAAACT[A/G]CAGGTACAAGTAACT | 57690 |
rs184844894 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089554 | CCATGGTCAGTAGTG[C/G]GGGCTCCTAGCTACC | 57690 |
rs184915901 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027342 | ATTAAATATTTGAAC[A/G]TGTTCAAGTGATGAT | 57690 |
rs184932544 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103225 | AACTGAAGCATCCAA[A/G]TTTTTAGTTACACGT | 57690 |
rs184942946 | snp | C/T | 0.000678302 | 0.0184036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067943 | GTACAACACTCTTAA[C/T]GACGGTACACCCTGA | 57690 |
rs185011653 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045537 | ATGGACGTGCTTGTT[C/T]AAAGCAGTCTGGGCT | 57690 |
rs185014010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022109 | GACTTTGCTGGCCAT[A/G]TATGGTCTCTGTCAT | 57690 |
rs185029250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008243 | GCATGCTTTCCTACC[C/T]TCCCCCAACAAATTT | 57690 |
rs185040029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061443 | CTTCTAGAACCTTTA[A/G]AGTGTCAGATGGTAC | 57690 |
rs185058659 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083742 | GAACTTAATTCTCTC[A/G]TGAAACCCCGGTCAA | 57690 |
rs185062131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040253 | GAATGCCACCTGATC[A/G]TGTCAGGTTCAGTGC | 57690 |
rs185130819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081948 | GATCTCTGAAGACTT[G/T]CCTTCTTCCTTCCCT | 57690 |
rs185149902 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065484 | AAAGTCAAAGCAACC[C/G]CGCATATTATGTTTG | 57690 |
rs185153127 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016322 | GGCACCCACAGCCAG[C/T]ACCTGCCAGGTCACA | 57690 |
rs185165604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100262 | GGACTTTGTGTGGGG[A/G]CTCCAACCCCACATT | 57690 |
rs185192756 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055239 | TACCTTTTAAACTTT[C/T]TTGATAACTAAGACA | 57690 |
rs185210337 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092682 | CCCAGGAGGTTGAGC[C/G]CTGATCACATCACTA | 57690 |
rs185266789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035909 | AAAAGTAATACATAG[A/G]TTTTCATTGTACTTT | 57690 |
rs185290418 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075690 | CACCCATCTCTGGCT[A/G]GCCCTTGTCAGTTGG | 57690 |
rs185323657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014161 | TCCACTTAAATCTTC[C/T]GTGTTTCATGAGATT | 57690 |
rs185354852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031902 | TGCTATTTTCAACTT[G/T]GCTGCTGAGCAATAG | 57690 |
rs185390634 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007388 | AAGGTTTACGTTTTT[C/T]TCAGACTCTTCATTA | 57690 |
rs185438131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075833 | GTGTGACTGCAAAGC[A/G]GAGAAAAGCATTGCA | 57690 |
rs185561991 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026082 | TTTTTGAGGTCTCTA[G/T]CCTTAGTATTTTTTT | 57690 |
rs185565356 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055435 | CTTGCTGTGACTGGC[C/T]GCACAGTAGGTTTGT | 57690 |
rs185584794 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014409 | GTCTTGATTACTCAG[A/C]TTTAACATATGCTCT | 57690 |
rs185603004 | snp | A/G | 1.66109e-05 | 0.00288187 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093075 | CTGGTCACGTGCCAA[A/G]TCTGACAGTGATAAA | 57690 |
rs185610610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052288 | CCCATGTAGAGGACA[A/G]GAACAGAGAACTGAC | 57690 |
rs185612816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073301 | TGAATCGCCAATGCC[A/G]TATTTGAAGCATGTT | 57690 |
rs185630258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033008 | TGCCAGCAGTTTACA[A/G]TCAAACATGCTACTT | 57690 |
rs185652156 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090555 | GTGCTGGTTATTCCC[C/T]TCCAAACAAGCAGTC | 57690 |
rs185687023 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031550 | CTGTTCAAGCCAGCC[C/T]CAACCTGCCGGTACC | 57690 |
rs185707886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072450 | GGGACTAGAGAGAGA[C/T]ATGGAGATGGGCCTC | 57690 |
rs185775443 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107946 | ACTTTCACCAAGCAC[C/T]TTGAGCACAGTGGAA | 57690 |
rs185817817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013937 | TGCTCTTTTGCCTAA[C/G]AGAATAAGAAGGCTT | 57690 |
rs185821641 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079616 | GTCCTGTGTTATCTG[C/G]AAGTCACTATTTTAA | 57690 |
rs185828191 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018315 | TATTTTTTTGAGTGG[A/C]GATGGGGTTTCACCA | 57690 |
rs185849028 | snp | C/T | 7.28505e-05 | 0.00603489 | missense | TNRC6C | GRCh38.p7 | 17:78050663 | AAGCGCCAAGTGGCC[C/T]GGGGGTTTGGGGGGA | 57690 |
rs185850092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057757 | TTTGGGTTTTAAGTT[A/G]TGGATCATTACCACT | 57690 |
rs185854267 | snp | A/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011180 | TTTTCTGTGTTTTTT[A/T]AAAAACAACTTTATT | 57690 |
rs185869147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036635 | AATTAGAGAAGAGAC[G/T]TACATAGGCCGGGCG | 57690 |
rs185885633 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076475 | AACTGATAAAATTAC[G/T]GTTATCTGAAATTCC | 57690 |
rs185889342 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009239 | CCATAATGAGTAATC[A/C]GTTTTCTTTATTTTT | 57690 |
rs185894391 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094493 | GCCCAGGCTGGAGTA[C/T]AGTGGCGTGATCTTG | 57690 |
rs185900075 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084867 | CAACTCCTTACCTCA[C/G]GTGATCCTCCCGCCT | 57690 |
rs185941534 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038551 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 57690 |
rs185990767 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024656 | AGGCGTGAGCCACCG[C/T]GCCTGGCCTATTTAG | 57690 |
rs186000598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051530 | TATTCATGAATACTC[C/T]GAGTAGTGTTTTTTA | 57690 |
rs186017577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090039 | TAGATCTGTACAAGC[C/T]GAAACGAAAAGAACC | 57690 |
rs186118865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072634 | ACACCTGTAATCCCA[A/C]CACTTTGGGAGCCCA | 57690 |
rs186122653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004792 | TCTTGTAGTTTAAAC[A/G]GTATACCTATTAGAG | 57690 |
rs186151936 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043762 | CCTAGCCTCTATCTT[C/T]ATAAGTTCAATTATG | 57690 |
rs186158957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038344 | TGAACGGGAAGATCA[C/T]AGAACTACCACAAAT | 57690 |
rs186165089 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084646 | TTTTTTTGAGACGGC[A/G]TCTTGCTAGTCTTGC | 57690 |
rs186175144 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019891 | CTTTGATGCCCTGGT[G/T]TTTTAGACAGTAATA | 57690 |
rs186200679 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106780 | AAGTATGTTTTAAAA[A/T]ATATATATATGAACA | 57690 |
rs186202819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059434 | GGGAGCCTGCTACGG[A/G]AGTAGGAAGAGATGC | 57690 |
rs186206584 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003330 | CAGAGAGTATCTAAG[A/G]GAAGAGGCATCCAGA | 57690 |
rs186207159 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078818 | AAAAACACAAAAATT[C/T]GGGGTGGCTCACACC | 57690 |
rs186229229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041201 | GCTTCTCGCCAGTCC[A/G]TTTGTGACATAACAT | 57690 |
rs186395216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063017 | TTGGGAGGCTGAAGC[A/G]GGGGGATCACTTGAG | 57690 |
rs186405868 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023541 | CTGGGCACAGTGGCT[C/T]ATGCCTGTAATCCCA | 57690 |
rs186423689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042450 | GGTCAGCTAAGCCGA[C/T]GTGTATGGAAATACT | 57690 |
rs186429961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024255 | TCAGTTTTATTTGGA[A/G]AGTTTGCTATTGTGA | 57690 |
rs186434375 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003917 | TCCATATCATACCCT[G/T]ATCCCCAGCAATGCC | 57690 |
rs186437873 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081565 | TTAAACTAGGTAGAC[A/G]TTGATCTCTCTCAGG | 57690 |
rs186446014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064215 | ATTCTCCTGCCTCAG[C/T]CTCCCCAATAGCTCG | 57690 |
rs186462647 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078986 | TAATCCCAGCTCCTC[A/G]GGAGACTGAGACAGA | 57690 |
rs186466123 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030518 | CATTGCAACGGCTGT[G/T]TCACCAGACGATAGG | 57690 |
rs186468402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048589 | TGATGTGCTAACGTG[C/T]ATTGTGAGTATTCTC | 57690 |
rs186469716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096250 | GGGAGCAGCAGACAC[C/T]GGGGCCTGCTGTATG | 57690 |
rs186479193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059943 | TCTGTATTAGTATCG[A/T]GAAATCAAAACTGTA | 57690 |
rs186480194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012472 | GTGTAACAAACCTTC[A/G]TATGTACCTCCTAAC | 57690 |
rs186507864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029220 | CTGACACTAAAATTC[A/T]GTAGTACGATCATAC | 57690 |
rs186519722 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069533 | GGTCTACAGGTGCAT[A/G]CCACTCTGCCCAACT | 57690 |
rs186546712 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074360 | TGCCCCAATTACTGA[A/T]TTGGGGGTTACAAAT | 57690 |
rs186698756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033944 | CCCTCACAAACCTGC[C/T]GTGGTCACCTAGTTA | 57690 |
rs186703645 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053616 | CCTGGGCGACAGAGC[A/G]AAACTCTGTCTCAAA | 57690 |
rs186710361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015281 | TCATCTATTCAATAA[C/T]GTCCTGTTGACAGAG | 57690 |
rs186763404 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047355 | AACCTAGTCATTTTA[A/T]AGCAGTTTCAACATT | 57690 |
rs186788222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059050 | TGTTTCTATAAGTCT[C/T]ATTAGCAGCAGAAGC | 57690 |
rs186788787 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090965 | TATCCCAAAACAAAG[A/G]AAGATTTTCCTAATA | 57690 |
rs186803694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019438 | TGTGGGAATCTCTCT[A/G]TTTGGCCCTGTTATG | 57690 |
rs186805521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095510 | CATCGTTTGACTTCC[C/T]GGGTGCTCGACGTTT | 57690 |
rs186895737 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102762 | TAACCATGTTCCTGG[C/T]GAATTGTTTGTTTCC | 57690 |
rs186947004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034509 | TGTCCCCCCGCACCC[A/G]TGAGGCTTCCCCAAG | 57690 |
rs186963494 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075353 | ACTGTGTCCTTAATA[A/C]AAGCCAGATTAAAAA | 57690 |
rs186972788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092135 | CCATAGGAGGTAATC[C/T]CACTCTCAAGCATTA | 57690 |
rs186973173 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055089 | GTAGACTTGGTGAAC[A/G]CTGTACGCTTAGGCC | 57690 |
rs186998179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037596 | GAGTGACCTGCATGC[A/G]TGAAAAGCGCAGACC | 57690 |
rs187033579 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078597 | ATTCATGTTGCTGTT[A/G]TGTGTGAAACATTGT | 57690 |
rs187078514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006015 | CTGTACATGTAGACA[C/T]ATGCACTCTCACAGC | 57690 |
rs187085211 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009910 | TTTTTGAGAGAGAGG[A/G]TCTAACTCTGTTGCC | 57690 |
rs187113037 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046628 | CCTGTTTATGTCTTA[C/T]GTATTTCATGTCTTC | 57690 |
rs187180954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038923 | GCGACCAGCGAGAGT[A/G]TGGGAAAAGGCGACG | 57690 |
rs187254081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028509 | TAGACAGTGGGTTCA[C/T]CCAGGACTAAGGACT | 57690 |
rs187287951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068988 | GAAAACATGAAAGAA[C/T]ATTAAAAACAATTTT | 57690 |
rs187295602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095811 | CACTTTGGGTGGCCA[A/G]CGTGGGAGAATCACT | 57690 |
rs187355355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066813 | GAAATGCAGCCTGTC[A/G]GGCCCAACCTCAGGC | 57690 |
rs187371617 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025931 | TTCACTTCAACCATA[A/G]GCTTTCAGAATTAGA | 57690 |
rs187373042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044886 | GGAGTCCTAACTAGG[A/G]AACAAAAACGTCCCA | 57690 |
rs187385193 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082792 | ATCCATTTATAGGCT[C/G]TCTGCAGGGGGAAGC | 57690 |
rs187391737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102232 | AAAACACAGGCCTCC[C/T]GGGCTGGTGGGAAGA | 57690 |
rs187409306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099182 | GCATAGTGGCACATA[A/C]CTGTGATCCCAACTG | 57690 |
rs187459146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109268 | CATGGCGAGCCCCGA[C/T]TGAGTGTTCAGTGAA | 57690 |
rs187464199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071985 | CAGATGGCAAGGGAT[A/G]TCGCCCATATTCGCC | 57690 |
rs187534524 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011967 | CTTTTAAAGTCTTTT[C/G]CCCATTTTTCATTGT | 57690 |
rs187556187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047856 | TTGGAATAAAGTCTG[A/C]CAAAAAGTTGATCGA | 57690 |
rs187572825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070509 | GCCCTCCCCCACCCC[C/T]ACTGCTCTTTCTGTA | 57690 |
rs187583305 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108698 | AAAGACCTCGTGGGC[C/G]TGGGTGTCCAGGGCA | 57690 |
rs187594106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086264 | GAACCCGGGAGGCAG[A/G]GGTGGCAGTGAGCTG | 57690 |
rs187662387 | snp | A/C/T | 0.000550866 | 0.0165872 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091415 | TAGAGGAGCAGGCGA[A/C/T]TCCTAACCGCATCTC | 57690 |
rs187665600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067410 | TTTAGGAATCTACAT[A/T]TCTGTAGCCTTTTCA | 57690 |
rs187700185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087796 | ACTTGTAGAAGCACA[C/G]TCAGCACTTGAAACC | 57690 |
rs187850513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108909 | GCAGTGATGTAATCT[C/G]GGCTCACTGCAACCT | 57690 |
rs187890433 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097236 | ATCTCTTAAAAAAAA[A/T]TTTTTTTTAAGCAAA | 57690 |
rs187917736 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082377 | AGAAGTACAGTATAC[A/G]GGGATAAGAATTTAC | 57690 |
rs187918062 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044762 | GACAGAGACTATATG[A/G]CCCACAAAGCCTAAA | 57690 |
rs187923780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016249 | CAGCCACAAAAGGAG[C/T]GATTGGGAATGTGGC | 57690 |
rs187946881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045196 | TGGAAAGTTATTTAC[A/G]GTAATCCAGTCAAGA | 57690 |
rs187965510 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074759 | ACCACTGAGCCCACC[C/G]GAAATGAGGAAGCAA | 57690 |
rs188075191 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007108 | CCTCGGCCTGCCAAA[A/G]TGCTGGGATTACAGG | 57690 |
rs188139030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097675 | TCCTGATGGTTCTCA[C/T]ACCCCACAGTTAGAG | 57690 |
rs188157309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080305 | TACAAAATTAGCCAG[G/T]TGTGGTGGCGCATGC | 57690 |
rs188167619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025485 | AGTTTATCCATTCAC[A/G]TACTGAAAAACATCT | 57690 |
rs188194321 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066353 | TGTGGTTTTTTTTGG[G/T]TTTTTTTGTTTTTTG | 57690 |
rs188233282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101763 | CTTAAGGCACAGATC[A/G]CTCGTGCTACTGTTT | 57690 |
rs188361362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018167 | GAGTCTTGCTCTGTC[A/G]CCAGGCTGGAGTGCA | 57690 |
rs188388858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055574 | GGGGACCATTGTCCT[A/G]TACGCAGTCAGTTGA | 57690 |
rs188393297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076148 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTAAGC | 57690 |
rs188395128 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036517 | AGGAGCAGAAATGGG[A/C]AAGTTTTTAAAGAGT | 57690 |
rs188425614 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021941 | TATATTACCAGGATT[A/T]TTCCTCTGGAAGGTT | 57690 |
rs188449556 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020636 | ATGAATCATTTTAAA[C/T]AGGCTAGTTGCATCA | 57690 |
rs188491949 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096596 | TATTCACTGCACAAC[A/C/G]CCATGTGGGCCTACG | 57690 |
rs188516536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008629 | TGACATCCTGCACTC[C/T]TAAGGAGTCTGGGCA | 57690 |
rs188663169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057948 | TAGTATTTTAGGAAA[C/T]GCAGTATAGCTTCCT | 57690 |
rs188690735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076993 | CTTTTAAACTGAAAA[C/T]AGCATCTTAATCCTA | 57690 |
rs188700746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094498 | GGCTGGAGTATAGTG[A/G]CGTGATCTTGGCTCA | 57690 |
rs188701531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048178 | TTTATTATGAATGTG[A/C]AGGAGACAGTGATAA | 57690 |
rs188720263 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012222 | TAGTCACATTTTGCT[A/C]CCTAGAGATGGCTAG | 57690 |
rs188742003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079204 | CAGTGAGCCAAGACC[A/G]CGCTACTGCACTCCA | 57690 |
rs188749260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087573 | CTCCAAAGTTTGTTC[C/T]GTTCCTAGTCTACTC | 57690 |
rs188750259 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040036 | TAGGCCAGGGTGCCT[C/G]CCAGCCCTGGTTCCA | 57690 |
rs188776188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046470 | GGCGAGAGCCACTGC[A/G]CCTGGCCGGGAATTC | 57690 |
rs188778424 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028267 | TTTTCTGGGGATGGG[A/G]AGAAGTGGGAACAAG | 57690 |
rs188784296 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009805 | TGATCTGCCCACTTC[A/G]GCCTCCCAAAGTGCT | 57690 |
rs188796834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084176 | GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 57690 |
rs188814325 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068625 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 57690 |
rs188829031 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105487 | CATATCAAACATGCA[A/G]ATACTTGAATCCAGC | 57690 |
rs188968511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033444 | GGAAGCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 57690 |
rs188974733 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002489 | CTCACTGCATTTTAT[A/G]CTTGTTGCTGTTGTA | 57690 |
rs188994090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029885 | AGTATCACTATCTTC[C/T]ACCTCCACATCTTGT | 57690 |
rs189004394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041170 | AAACGGAACAAACAC[A/G]GAACAAATAGTGGCT | 57690 |
rs189011767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031215 | GGGCTCTGATAAGCC[C/T]TCTAGGTGATTGTGA | 57690 |
rs189021676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070789 | ATTATTGGATAGTAA[A/G]AGTAGTCTATATTTG | 57690 |
rs189027596 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013447 | GATAGAGTAGGCAGA[A/T]CTTAGAAACTAACTG | 57690 |
rs189044098 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089498 | ACCTATGTTGAAGAG[C/G]CTGTTAGACACTCAT | 57690 |
rs189050189 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023760 | ACAGTGAGCTGTGAT[C/T]ATGCCACTACACTTC | 57690 |
rs189050450 | snp | A/G | 0.00140633 | 0.02648 | missense | TNRC6C | GRCh38.p7 | 17:78050327 | GAGAAGGCCGAAGGC[A/G]AGATAAAGGGATTAT | 57690 |
rs189054380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072111 | ATGGCCTCCATGTAG[C/T]GGAGGAACCCCATCC | 57690 |
rs189054540 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003660 | TGTTTTCAAGAAAAT[A/G]GAGAACTGAAAGGTA | 57690 |
rs189242548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052867 | AACCAGAGGTCAAAA[A/G]TCAGTGGTCCGTGGG | 57690 |
rs189254433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014462 | CTTCTAAATAAGCCT[A/G]TTGTTTAAAAAGAAC | 57690 |
rs189259388 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026447 | CTATTTTATGTACCA[C/G]TAAGAAAAAAATTGC | 57690 |
rs189294099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062820 | AGGGTTACCAAAAGT[A/G]TAACTTAGGACTTCC | 57690 |
rs189306225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023240 | GTGGATTTTGGCATC[C/T]AAGGGGGTTTCTGGA | 57690 |
rs189318634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094060 | TCTCAGCTCTCTGCA[A/G]TCTCCACCTTCTGGG | 57690 |
rs189350609 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090314 | TTTGCCACAGTCCCC[A/C]TGAAGCCCACTTCTT | 57690 |
rs189396895 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022172 | AAAAATGTAAGGGGC[A/G]TTCTTACTTCACCTG | 57690 |
rs189417211 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061668 | TTCAGCCCAGGCAAC[A/G]TAACAAGACCCCATC | 57690 |
rs189439072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040335 | GCTTTTATCTTTAAA[A/T]AATAATAATAATAAT | 57690 |
rs189456642 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079709 | TTTTAGACTATAAAG[C/T]AGTAAATGGATTCTC | 57690 |
rs189511536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007875 | ATTACACACCACTCA[A/G]CTAGTAGCATTCGTA | 57690 |
rs189532922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045555 | AGCAGTCTGGGCTGT[A/G]CAAGTGCAGCTGATT | 57690 |
rs189567508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019073 | CAGAAGTATGGATAG[C/G]AAGCATAGTGAAAGG | 57690 |
rs189569401 | snp | A/G/T | 0.00438556 | 0.0466571 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084012 | GAATCGGCCGGGCAC[A/G/T]GTGGCTCATGCCTAT | 57690 |
rs189633659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101056 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 57690 |
rs189676428 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014197 | TTTGCCATTTGTTCT[G/T]AGAGCTCATTTAGTT | 57690 |
rs189711674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072925 | TGAAGAAATGTATTT[C/T]CAGTTCCAAAACCTA | 57690 |
rs189717384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032542 | CAAAGTATTTGTGGT[C/T]AACTGCCATGTTCTC | 57690 |
rs189719858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051656 | TTTTCTATTCAAGAA[A/G]AAAATATATTAAGCA | 57690 |
rs189820714 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075747 | TGTGGAAAACGCCCT[A/G]AATGTTTAGCCAGTC | 57690 |
rs189827581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103254 | GTTTGGCCACAGAGA[G/T]ATAAAACGTTAATGT | 57690 |
rs189833363 | snp | A/G/T | 6.98849e-05 | 0.0059108 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067947 | AACACTCTTAACGAC[A/G/T]GTACACCCTGAAAAC | 57690 |
rs189834953 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036179 | TTTCAGCTTCGCACA[C/T]GAATTTCTGTGTTTT | 57690 |
rs189839889 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037335 | ATTTGTTGAATGCCT[A/C]CCAAACATCACATAC | 57690 |
rs189855133 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020131 | GGTGTACAGCTCAAC[A/T]GGGTCAGAATTCCGC | 57690 |
rs189870625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096076 | AAGGCCTCCCAAAGC[A/G]CTGGGATTACATGCG | 57690 |
rs189876020 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059480 | CGTGGCGTGAGACGT[A/G]TGAACCCCACATGCA | 57690 |
rs189880005 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107050 | TCTCATTGCCATTAC[A/G]TGCGTTCTATATATT | 57690 |
rs189883707 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078916 | GCCAACATGGTGAAA[A/C]CCCGTCTCTACTAAA | 57690 |
rs189958183 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076143 | ATTGCTTGAACCCGG[A/G]AGGCGGAGGTTGCAG | 57690 |
rs190053848 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016691 | TCTTTAGGTCATTCT[A/C]TGTGGTTCCTCCTTT | 57690 |
rs190088526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055325 | TGTCCACCTCCACAC[A/G]TTGTCCCATTGGAGA | 57690 |
rs190118947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097923 | CCCAAACAAAACTTT[G/T]ACAGGCCCCAGCTTT | 57690 |
rs190129301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063752 | TTATGTTTTTAATCT[A/G]CCATCTTCTCATTTC | 57690 |
rs190232977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011810 | TCTGCATCTTCACCA[A/G]TGTGTGGTATGGTCA | 57690 |
rs190263878 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029255 | CTTGACAGAGAGATA[A/C]GTTCTGAAAAATGCA | 57690 |
rs190265721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047625 | AAATTCATGTTTTAA[C/T]TGTCCATACGATTTT | 57690 |
rs190337036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041286 | TGGATAAAATGGCGT[A/C]TTGGAAAAGAGCTGC | 57690 |
rs190345466 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013979 | TTTGAAATAAGGCCA[A/G]TTTCTCTCCTCCTGC | 57690 |
rs190370971 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089928 | TGACTTTCCCAGAGG[A/G]GAAAGTTGGGAGAGA | 57690 |
rs190384092 | snp | A/T | 4.97971e-05 | 0.0049896 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050916 | AAAAAATGGATCTGG[A/T]TGGGATGCTGACAGT | 57690 |
rs190387530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081355 | GATGCACTGGGCACT[A/G]CATTGAGGGTAATTC | 57690 |
rs190517757 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047952 | TAGATCCAAACAGGG[A/G]ATTCTTTAAAAGGAC | 57690 |
rs190521968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070651 | TCCTTTCTTCTTGCT[A/G]CCTCTTTACTCATTG | 57690 |
rs190536795 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029566 | GTGAGTGGTGAGTGA[A/C]TGTGAAGGCCTAGGA | 57690 |
rs190541141 | snp | A/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108805 | TTTTAAGTTTATTAA[A/T]TTTTTTTTTAAATGG | 57690 |
rs190558790 | snp | C/T | 0.00150797 | 0.0274173 | missense | TNRC6C | GRCh38.p7 | 17:78086941 | TGAAGCAGCCACCAC[C/T]GCCACCGCCCCCGCC | 57690 |
rs190594306 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031601 | CACTATCTCAAGCAG[C/T]AACAATGGCAAACGT | 57690 |
rs190612429 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072504 | GGAGAGCATCCTGTC[C/G]TCATGGCAGGTGTCC | 57690 |
rs190649901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005571 | GTTGGTGGAAACACA[C/T]GCATTTCTCACTGTT | 57690 |
rs190666077 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082079 | AATATAATTATTATT[A/G]CAGGATCTGGCCAGC | 57690 |
rs190674161 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044002 | AATCTTGGTTGTTGT[C/G]AGTAGTGCTGCAGCA | 57690 |
rs190760579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052489 | GTGGCAAACAACACA[C/T]GAATTAAAGTATATA | 57690 |
rs190802280 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073366 | GAAGGTAATAATGAC[A/C]CTCTGAGAGACACTG | 57690 |
rs190806339 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090743 | CTCAGCTCACCATCC[C/T]AGCTGGGGGCAGATG | 57690 |
rs190873593 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024380 | TTTGTTTGTTTGTTT[G/T]TTTGGAGATGGAGTC | 57690 |
rs190873681 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043571 | TTATCCATTGTGTTA[A/C]AAATAATCCTATTAT | 57690 |
rs190889001 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003941 | CAATGCCTGATGATG[A/G]GTTGGTGTTCAACAA | 57690 |
rs190892735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081672 | CAGCACTACTGTGCC[A/G]GTGGCCTTGAAATTG | 57690 |
rs190896600 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024889 | AGCCTCTGCCTCCAG[C/G]TTCAAGCAACTCTCC | 57690 |
rs190903780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099399 | TTTATAAAAGAATGA[C/G]ATTTATTGGACTTAC | 57690 |
rs190906501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064304 | GTTTCACCATGTTGG[C/T]CAGACTGGTCTCGAA | 57690 |
rs190907798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069032 | CCTAACTATGACCAA[A/G]ATCTAAAAGCCATAA | 57690 |
rs190930175 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065665 | CTAACGCATCTTGCC[G/T]TATTGCCCTGCTTTC | 57690 |
rs191144055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010414 | CTCATTCTAAACATA[C/T]AAAGTTTAATATCAA | 57690 |
rs191157311 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034337 | GCTGTGATTCCAGGC[A/G/T]TGAGCCACCACCCCC | 57690 |
rs191163189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084708 | ATCATGGCTCACTGC[A/T]GCCTCTGCCTTGTGG | 57690 |
rs191167699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047000 | CGAATGGCACCTCAC[A/G]TATGGAAAAGAATGC | 57690 |
rs191170846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015792 | TGGTGGGCGCCTGTG[A/T]TCCCAGCTACTCGGG | 57690 |
rs191189338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091812 | CATTAGATCTTAGCT[A/G]CAAACTTAGAAATAA | 57690 |
rs191197470 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054902 | CGCTACCATACACCA[C/T]TGCGGACTACTGTAT | 57690 |
rs191201928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074916 | TGCAGGAGCCACGGA[A/G]GGGTGCCTGGGGCCA | 57690 |
rs191222397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084972 | AGGGAGGTGGTGCTG[C/T]AGTGAGGAATCGCTG | 57690 |
rs191425199 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069602 | ACTTTGTGGCATTTA[C/T]ACAGTTTTGTATTGC | 57690 |
rs191432874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012132 | AATATCAGAAAATAT[G/T]CACTTTCAAATAGAA | 57690 |
rs191433250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038028 | AGATCACTGAGAAAA[G/T]AGTGGTTCAGATCAA | 57690 |
rs191467954 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107958 | CACTTTGAGCACAGT[A/G]GAACTTCAGAAGCAC | 57690 |
rs191477012 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078636 | AGTTTCTTTGAATGG[G/T]GTAGCCTTCTTGTTG | 57690 |
rs191597521 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062147 | TTTGTAAAACTACTT[C/T]TCCCAATATATATTA | 57690 |
rs191610459 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022193 | ACTTCACCTGCCAGT[C/T]CTGCCCTACTCACAT | 57690 |
rs191612102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040811 | AATTAGATAATCAAA[A/G]CTGTAAAATCCCATC | 57690 |
rs191691143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059054 | TCTATAAGTCTCATT[A/G]GCAGCAGAAGCCAGA | 57690 |
rs191695856 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019796 | CTGATATGCAAAAGG[A/G]TAGGTTCCCATGTGA | 57690 |
rs191710599 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079122 | GGCATAGTGGCGGGG[A/G]TCTGTAATCCCAGCT | 57690 |
rs191713130 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78048969 | GACTGACAAGGAGGC[A/G]TGGCCTTCCATCACA | 57690 |
rs191714029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095617 | GCCTCCCCTTCAGCT[C/T]GTGACCAGCACGAGG | 57690 |
rs191714795 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030821 | ATGCAAATTCCGGCC[A/G]GGCATGGTGGCTCAC | 57690 |
rs191720999 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012575 | AAGCAAATATATGTA[C/T]ATGCAAATGAATGCA | 57690 |
rs191734602 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033156 | AGCCCTGCCTGTTCT[G/T]GTTGTATCTGGTTGT | 57690 |
rs191738218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066493 | TTAGATTCATGCGCC[A/G]TTTTGAGCATTCTAT | 57690 |
rs191746874 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096488 | CCTCAGCTCTGGTGC[C/G]CTCATTCTAAAGAGG | 57690 |
rs191756570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071988 | ATGGCAAGGGATGTC[A/G]CCCATATTCGCCATG | 57690 |
rs191784360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102025 | GGACACAGCCAAACC[A/G]TATCAGATAGTTGGA | 57690 |
rs191974285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053099 | GTCACGTTGCCCCCC[A/G]ACCCCTGACGGTTCC | 57690 |
rs191982663 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014510 | TATGATACATAGTAC[A/C/G]TTTTCTTACAGCAGG | 57690 |
rs191984574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014418 | ACTCAGCTTTAACAT[A/G]TGCTCTTAGCGGCAT | 57690 |
rs191986553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091187 | AGCACTAAAAGTTAT[A/T]GTTAAAATATTTTGC | 57690 |
rs192022261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089534 | CATGTAAAGAAACCA[A/G]CAGCCCATGGTCAGT | 57690 |
rs192032589 | snp | G/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022033 | CTGTAGGTCTAGCCT[G/T]TGGGCCAAAAAGATG | 57690 |
rs192043363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082458 | CAGTCTGTCCATAAC[C/T]TGTGTTTAGTAAGAT | 57690 |
rs192205428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007988 | ACATTTTCAAGGAAC[C/T]TTTTAGAATATATGA | 57690 |
rs192225070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045469 | CTACACCTCAAAGCC[C/T]GGGAAGGTCTGAGTA | 57690 |
rs192261950 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083467 | TCAGCCACCTGAGTA[C/G]CTGAGACACCACGGG | 57690 |
rs192273593 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075445 | AACTCAAAGAAGGGA[A/G]TGTCGTATTTCATAA | 57690 |
rs192282970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092379 | TCCACTGTGTTCTTC[C/T]GTAGTGAGGGTTTCA | 57690 |
rs192288352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025689 | GAATCAACTTCAACT[A/T]GTAACAAATAGGTTC | 57690 |
rs192289510 | snp | C/T | 0.030278 | 0.119257 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006583 | CCTTCTTCCTTCTTC[C/T]TCCTTCTTCCTTCTT | 57690 |
rs192298391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033665 | CAAGAGTGAAACTCC[A/G]TTTCAAAAAAAAAAA | 57690 |
rs192326314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044773 | TATGGCCCACAAAGC[C/T]TAAAGCATTTTGGCT | 57690 |
rs192333729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074462 | GTGCACGTGCGACAA[C/T]GTGTGGTGCAAACTG | 57690 |
rs192358544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079712 | TAGACTATAAAGTAG[C/T]AAATGGATTCTCCTG | 57690 |
rs192368676 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097433 | GAGGAAATCAGTGTG[A/G]TCCTTTAAAACTCTT | 57690 |
rs192506350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108910 | CAGTGATGTAATCTC[A/G]GCTCACTGCAACCTT | 57690 |
rs192515512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071619 | TCTCGAACACCTGGG[C/T]TCAAGCGATCTGCCC | 57690 |
rs192547711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066995 | GAACAATACAGAGAA[G/T]ATTCGCGTGGTTCCT | 57690 |
rs192553886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045103 | ACCCACTGGGCATTC[A/G]TTTGGAAAAGAGCAC | 57690 |
rs192556571 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026077 | CCAAGTTTTTGAGGT[C/G]TCTAGCCTTAGTATT | 57690 |
rs192558470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102604 | GTTCCCGCTTGGCCC[C/T]CAATGCAGATGAGGC | 57690 |
rs192570702 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082817 | GGAAGCACATCACGC[G/T]CTGTTGGCTCATTCT | 57690 |
rs192646786 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026762 | AGGATCACACTGGCT[G/T]CAGTATAGATGATGG | 57690 |
rs192660164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103133 | AGAGGCTCTGTGCGA[C/T]GTGCTCTGGTGAAAG | 57690 |
rs192667738 | snp | A/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78067907 | GGGGGAACGCCCCCA[A/G]AAAAGGACTTCAAAA | 57690 |
rs192712202 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020979 | CCCAGTTCATTGTTG[A/G]TTCACTTAAGTGAGA | 57690 |
rs192733586 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088432 | AGAGACAGGGTCTTT[C/G]TATGTTGCCCAGGCA | 57690 |
rs192795766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048243 | ACAGCTAATTAAACA[C/T]TTCTAATCCTTAGTA | 57690 |
rs192800960 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012349 | CTCCTTGAGGGTGGA[C/G]GGTGGAAGGAGGGAG | 57690 |
rs192813408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087588 | TGTTCCTAGTCTACT[C/G]TGAACTGTACTTTAC | 57690 |
rs192860150 | snp | A/G | 0.000149035 | 0.00863107 | missense | TNRC6C | GRCh38.p7 | 17:78079476 | CCGCCACAGCCACCA[A/G]TGCAGCCTCTTAACT | 57690 |
rs192861231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040224 | TACGTACAGTGATTT[C/G]CAGAGATTCCAAAGA | 57690 |
rs192916207 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039066 | GACTGAATGCTCTGC[A/G]TTTGTCCTCTGCCCA | 57690 |
rs192956739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109293 | AGTGAAGAGGGAAAA[C/G]AGAGACAGTGGGGCA | 57690 |
rs192981829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035209 | CTGTCCCATGTTGTT[A/G]CGGTGTTGGCACAGG | 57690 |
rs193061299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061081 | CATATCCTGGCTGTG[C/T]TTTATTATCCCCATC | 57690 |
rs193080625 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096945 | CTAAGTCTCCCTTTC[A/G]GGCACAGGGACAAGC | 57690 |
rs193116800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055362 | AACAGGAAGTACAGT[A/G]AAGACATAAACTGGT | 57690 |
rs193122978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092830 | GAATAGGGCAAGGCA[C/T]TGGACCTAGAACAGA | 57690 |
rs193193634 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016314 | TGCTTACAGGCACCC[A/G]CAGCCAGTACCTGCC | 57690 |
rs193201595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055222 | TATGAGCTTTTTTTT[G/T]GTACCTTTTAAACTT | 57690 |
rs193253997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007309 | CCAAACAAAAAATGC[G/T]TTTTGAATTATAAAT | 57690 |
rs193267927 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075749 | TGGAAAACGCCCTGA[A/G]TGTTTAGCCAGTCCG | 57690 |
rs193269996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036242 | CCCTCCCCCCAGGTT[G/T]TAGTGTGCTTAGCGA | 57690 |
rs199505620 | snp | A/G | 9.33158e-05 | 0.00683002 | missense | TNRC6C | GRCh38.p7 | 17:78091553 | ACGCACCCCAACTCC[A/G]TGGATAACTTGCCCA | 57690 |
rs199549071 | in-del | -/AAAAAAAAAAAGAAAAAGA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076216 | GCGATACTCTGTCTC[-/AAAAAAAAAAAGAAAAAGA]AAAAAAAAAAAGGAA | 57690 |
rs199605179 | snp | A/G | 9.97258e-05 | 0.00706066 | missense | TNRC6C | GRCh38.p7 | 17:78050506 | GAGGCCTGGGGTTGT[A/G]CAGCTACTCAGGCTT | 57690 |
rs199612626 | snp | A/T | 4.97393e-05 | 0.0049867 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086978 | GTCTCTGCACCCCTC[A/T]GCAGGCAAATCGGCC | 57690 |
rs199678048 | snp | A/G | 8.28068e-05 | 0.00643402 | missense | TNRC6C | GRCh38.p7 | 17:78049592 | TCAGCGCACAACCTC[A/G]GAACCTTAACACTGA | 57690 |
rs199746293 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085854 | TTTGTTTTTTTTTTT[A/T]AAGTTTCAGTTTGTA | 57690 |
rs199760067 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059855 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAGAAAAAG | 57690 |
rs199763154 | in-del | -/TCTC | 0.00835141 | 0.0640778 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016227 | GCGGCACTAACACTG[-/TCTC]TCTCAGCCACAAAAG | 57690 |
rs199768638 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043348 | TGGGAGAAAAGAGAT[A/G]GTTGGTTGGTTGATT | 57690 |
rs199772685 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040704 | GAAGAAAAGTGGCTG[G/T]GATGCTAATTGTAAC | 57690 |
rs199781524 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047165 | GGTAATATTTGCTGG[A/C]AACAAGCCATAATCT | 57690 |
rs199795094 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079090 | AGCAAAACTCCATCT[-/A]AAAAAAAAAAAAGCC | 57690 |
rs199823268 | snp | A/C | 0.00299544 | 0.0385843 | missense | TNRC6C | GRCh38.p7 | 17:78049429 | GTGGCGACAGGCAAC[A/C]CTTCCAGTATTTGCA | 57690 |
rs199824689 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006828 | TTTATTTATTTATTT[A/T]TTTTTTTTTTTTTTG | 57690 |
rs199849871 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106555 | AACAAAACAAAAAAA[A/T]GAAAAAAAAGAAAAA | 57690 |
rs199858938 | in-del | -/TT | 0.23846 | 0.249734 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094441 | TGCTTCTTTTGTTTC[-/TT]TTTTTTTTTTTTTTG | 57690 |
rs199892751 | snp | A/G | 3.09746e-05 | 0.00393527 | missense | TNRC6C | GRCh38.p7 | 17:78051109 | AACTGGGGAGGAGCT[A/G]CTTCTGTGAAACAGA | 57690 |
rs199909963 | snp | A/C | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003171 | GGTTGGACTGGTAAA[A/C]CAGCCAGTTCCCTAC | 57690 |
rs199992060 | in-del | -/A/AGCGAGCTTCCGACC | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108959 | AGCGATCTTCCGACC[-/A/AGCGAGCTTCCGACC]TCAGCCTCCCAAGTA | 57690 |
rs200025310 | snp | A/G/T | 0.00049302 | 0.0156943 | missense | TNRC6C | GRCh38.p7 | 17:78049222 | GCCAGAGTGTGGGGT[A/G/T]TAGCCACAGGCTCCA | 57690 |
rs200064526 | in-del | -/G | 0.0655868 | 0.168795 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024983 | ATTTTTAATAGAGAC[-/G]GGGTTTCACCATGTT | 57690 |
rs200084854 | snp | A/G | 0.00364726 | 0.042548 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098416 | CTCTCTGTCTCATGA[A/G]CTATGGAAGGTGCCC | 57690 |
rs200092728 | snp | G/T | 0.000149533 | 0.00864546 | missense | TNRC6C | GRCh38.p7 | 17:78049445 | CTTCCAGTATTTGCA[G/T]TCCAGTCAGTGCCAT | 57690 |
rs200098437 | snp | A/T | 1.66338e-05 | 0.00288386 | missense | TNRC6C | GRCh38.p7 | 17:78086896 | AGCAGATCCAGCAGC[A/T]CCAGCGCCAGCTGGC | 57690 |
rs200101591 | snp | C/T | 0.000775155 | 0.0196717 | missense | TNRC6C | GRCh38.p7 | 17:78049255 | TCTGGCCTGGCTCAC[C/T]GCTCTGTCAGTGGTG | 57690 |
rs200140495 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006831 | TTTATTTATTTATTT[-/A]TTTTTTTTTTTGAGA | 57690 |
rs200187152 | snp | A/G | 4.98235e-05 | 0.00499092 | missense | TNRC6C | GRCh38.p7 | 17:78092999 | ATGACTCCTATGGCC[A/G]GTACGATTTAATCCA | 57690 |
rs200217894 | snp | A/G | 0.000560614 | 0.016733 | missense | TNRC6C | GRCh38.p7 | 17:78050746 | GCTTGGAGTGGGGCC[A/G]CAAATCAGGAGGACA | 57690 |
rs200219889 | snp | A/T | 0.0029955 | 0.0385847 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78048950 | ATAAAGTGATAATAG[A/T]TAGGACTGACAAGGA | 57690 |
rs200226260 | snp | A/G | 0.000298092 | 0.0122048 | missense | TNRC6C | GRCh38.p7 | 17:78049582 | AATGTGTCTTTCAGC[A/G]CACAACCTCAGAACC | 57690 |
rs200296226 | snp | A/G | 7.21007e-05 | 0.00600376 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102557 | CAGGTGCAATATGGT[A/G]CCCCTGCATCACTGA | 57690 |
rs200353045 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074176 | GGGGACCATTTTAAA[-/C]ACCAGAATCACTACA | 57690 |
rs200356688 | in-del | -/CAA | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106534 | TTTAAAAAAAAAAAA[-/CAA]AACAAAACAAAACAA | 57690 |
rs200368535 | snp | A/G | 0.000354442 | 0.0133077 | missense | TNRC6C | GRCh38.p7 | 17:78102491 | TCTGCCTGGAGCACC[A/G]ACACCTCAGGAAGAA | 57690 |
rs200406635 | snp | C/T | 0.0028242 | 0.0374716 | missense | TNRC6C | GRCh38.p7 | 17:78050768 | AGGAGGACAAGTCAC[C/T]CACCTGGGGTGAGCC | 57690 |
rs200409654 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056866 | AAATAATTCTCTTTT[A/T]TATGAAAAATATTTA | 57690 |
rs200491209 | snp | C/T | 0.00299544 | 0.0385843 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049434 | GACAGGCAACCCTTC[C/T]AGTATTTGCAGTCCA | 57690 |
rs200501711 | snp | A/G | 9.14369e-05 | 0.00676093 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075325 | TTTTTAACAAGAGGA[A/G]TTTTTCATTTCAACT | 57690 |
rs200649984 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075907 | AAGGAAGGACACATT[-/A]AAAAAAAAAAGATCA | 57690 |
rs200678920 | snp | A/G | 0.00299553 | 0.0385849 | missense | TNRC6C | GRCh38.p7 | 17:78049847 | CCACAGGAAATAGCA[A/G]TTCTGGGTTCAGTCA | 57690 |
rs200752661 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002857 | GTTGTATAGTTCTTC[A/G]GTGATTGAATTAGTG | 57690 |
rs200769817 | snp | G/T | 0.000233007 | 0.0107912 | missense | TNRC6C | GRCh38.p7 | 17:78049982 | CTCCTGCTGGTCCTG[G/T]AATACTCGCCTGGGG | 57690 |
rs200772794 | snp | A/G | 8.32203e-05 | 0.00645006 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098407 | CACGCAAGCCTCTCT[A/G]TCTCATGAACTATGG | 57690 |
rs200805438 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085856 | TGTTTTTTTTTTTTA[A/G]GTTTCAGTTTGTATG | 57690 |
rs200817030 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005869 | TTCAAAATAAAATGT[-/A]AAAAAAAAAAGACTA | 57690 |
rs200823380 | snp | C/T | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78091494 | TGACCGGTGGCTTGT[C/T]GGTGAAGGACCCATC | 57690 |
rs200889517 | snp | C/T | 1.6563e-05 | 0.00287771 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049569 | GTCCACTTCTCAGAA[C/T]GTGTCTTTCAGCGCA | 57690 |
rs200911250 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084294 | AAGAAAAAAAAAAAA[-/A]GAAAATCATGACCAG | 57690 |
rs200913054 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062351 | TGCATTTTCTTAGAA[A/T]AAGAGTATCAAGGGA | 57690 |
rs200917953 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015738 | CCAAGATGGCAGAAC[C/T]GCATCTCTACTAAAA | 57690 |
rs200956193 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007215 | TTCTATATCCTCTAA[A/G]ATACTGTTCCTTTGG | 57690 |
rs200983108 | snp | C/T | 0.000145143 | 0.00851766 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075251 | CTCCAAAGAGTCTTC[C/T]GTGGACCGCCCCACC | 57690 |
rs201018776 | in-del | -/ATT | 0.0444908 | 0.142359 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006683 | GCTATATTCTTCATC[-/ATT]GTCACTGTTTTCTAC | 57690 |
rs201082973 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106055 | ATATAAAGTTAAAGA[A/G]AAAAAAAAAAAAAAC | 57690 |
rs201090998 | snp | A/G | 0.000166326 | 0.00911785 | missense | TNRC6C | GRCh38.p7 | 17:78049414 | GGACATGAAGGAACC[A/G]TGGCGACAGGCAACC | 57690 |
rs201124248 | snp | A/G | 0.000149391 | 0.00864137 | missense | TNRC6C | GRCh38.p7 | 17:78083131 | ATTAATCCTCAACAT[A/G]TGACGATGTTGAACC | 57690 |
rs201125961 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013145 | TGTTTTTCAGCTCTT[C/T]TGAGAGAGGTGGAAG | 57690 |
rs201133108 | snp | C/T | 0.0039921 | 0.0444985 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051084 | CAAACCCCAAGACAA[C/T]AATGTGAGTAACTGG | 57690 |
rs201184976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102553 | TCCCCAGGTGCAATA[C/T]GGTGCCCCTGCATCA | 57690 |
rs201217429 | snp | C/G | 5.09092e-05 | 0.005045 | missense | TNRC6C | GRCh38.p7 | 17:78051002 | GCAACAGCACAAATA[C/G]AAAGGCCAATCCAGG | 57690 |
rs201237649 | snp | C/G | 0.000166525 | 0.00912331 | missense | TNRC6C | GRCh38.p7 | 17:78098507 | ACCTGGGGTGCCAGC[C/G]CCCTCGGCTGGACCA | 57690 |
rs201251847 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061044 | GATGAAGAATGTATA[-/T]TTTAAAATTGAATGA | 57690 |
rs201277309 | snp | A/C | 0.000549967 | 0.0165735 | missense | TNRC6C | GRCh38.p7 | 17:78091581 | CCAGTGCCGCTTCCC[A/C]CCTGGAGCAGAACCC | 57690 |
rs201297109 | snp | A/G | 3.31917e-05 | 0.00407367 | missense | TNRC6C | GRCh38.p7 | 17:78049921 | AATGGATCCAGCAGT[A/G]CTGTGCAAAAGGAAG | 57690 |
rs201333824 | snp | C/T | 6.7571e-05 | 0.00581214 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049194 | AGGGGGAGCGAACAG[C/T]AATGGAAGTGCGGCC | 57690 |
rs201339724 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077424 | CTTACTTATTTATAG[C/T]TAATACCTCTATTTT | 57690 |
rs201428494 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029617 | ACACTAAACTTACTT[-/A]AAAAAATTTTTTTTC | 57690 |
rs201430731 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022392 | AAATGGACTGATAAC[A/T]TTCATCTATGATTTG | 57690 |
rs201521961 | snp | A/G | 3.45823e-05 | 0.00415812 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093593 | GGTGTTCTGATCTGT[A/G]GCTTCTCATTTTGGT | 57690 |
rs201528132 | snp | A/G | 0.000772032 | 0.0196321 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087127 | TCAACAGCCACATCA[A/G]GTAGAGAGGGTACCT | 57690 |
rs201565230 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085857 | GTTTTTTTTTTTTAA[G/T]TTTCAGTTTGTATGA | 57690 |
rs201644892 | snp | A/G | 0.0039921 | 0.0444985 | missense | TNRC6C | GRCh38.p7 | 17:78050674 | GGCCCGGGGGTTTGG[A/G]GGGACTCGATAAGCT | 57690 |
rs201680674 | snp | A/G | 0.000961908 | 0.0219096 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78049040 | CTGACTCTGCCTCCA[A/G]CTGTGGCTCAGAGAA | 57690 |
rs201681149 | snp | A/G | 0.00063146 | 0.0177576 | missense | TNRC6C | GRCh38.p7 | 17:78049427 | CCGTGGCGACAGGCA[A/G]CCCTTCCAGTATTTG | 57690 |
rs201689202 | snp | A/T | 0.0003002 | 0.0122479 | missense | TNRC6C | GRCh38.p7 | 17:78050855 | GTGCAGGAGGGGGAG[A/T]TTGGGCAGATTCATC | 57690 |
rs201742845 | in-del | -/TTCTTCTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006493 | TCTTCTTCTTCTTCT[-/TTCTTCTTC]TTCTTCTTCTTCTTC | 57690 |
rs201743013 | snp | A/C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061639 | ATGATCACACTTAAG[A/C/T]ACAGCCACTGCACTT | 57690 |
rs201770136 | snp | C/T | 0.000248973 | 0.0111546 | missense | TNRC6C | GRCh38.p7 | 17:78083135 | ATCCTCAACATATGA[C/T]GATGTTGAACCAGCT | 57690 |
rs201771213 | snp | C/T | 0.0171979 | 0.0911217 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097707 | CATGAACCCGGACAC[C/T]GCCACCACCTTGCTC | 57690 |
rs201778814 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075404 | AGTGACTTTTATCCA[-/T]TTTTTTTCTAACATT | 57690 |
rs201793215 | in-del | -/C | 0.0490535 | 0.14873 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082688 | CCATTTATAGGCTCT[-/C]CCCAAGGGTCGCATT | 57690 |
rs201817980 | snp | C/T | 5.04214e-05 | 0.00502077 | missense | TNRC6C | GRCh38.p7 | 17:78098394 | GCCCTACCTCCCACA[C/T]GCAAGCCTCTCTGTC | 57690 |
rs201821181 | snp | A/G | 0.000120377 | 0.0077572 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067932 | TCAAAAGGTAAGTAC[A/G]ACACTCTTAACGACG | 57690 |
rs201836492 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064653 | TTTTGAAATTGAAAA[-/C]TGAATTATATTTTTG | 57690 |
rs201839982 | in-del | -/TTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006473 | TTCTGGATCATCCAT[-/TTC]TTCTTCTTCTTCTTC | 57690 |
rs201855896 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035321 | CCACCTCCTGTGTGA[C/T]CTTGACCAAATCACC | 57690 |
rs201856652 | snp | A/G | 0.000571237 | 0.0168906 | missense | TNRC6C | GRCh38.p7 | 17:78067774 | TCAAAATCTATGCAA[A/G]AAGGCTGGGGCAGTG | 57690 |
rs201919223 | snp | C/T | 1.65729e-05 | 0.00287857 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049521 | AGGTGCTTGGGGAAA[C/T]TTGCTGCCACAAGAG | 57690 |
rs201925366 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021574 | GTTATTTATTTTTTT[-/A]TTTTTATTTTCTTGA | 57690 |
rs201928909 | in-del | -/T | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012500 | ACCTAAAATAAAGGC[-/T]TTTTTTAAAAAAGTT | 57690 |
rs201980311 | in-del | -/AAA | 0.102726 | 0.202016 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051481 | TGTTTCTTTACAAGT[-/AAA]AAAAAAAAAAAAAAA | 57690 |
rs202000491 | snp | A/C | 6.35687e-05 | 0.0056374 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78102527 | AGCTGGCTCGTTCTT[A/C]GAAACCTCACTCCCC | 57690 |
rs202031086 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084621 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 57690 |
rs202067168 | snp | G/T | 0.000182335 | 0.00954644 | missense | TNRC6C | GRCh38.p7 | 17:78050699 | TAAGCTCTACTGCTG[G/T]TAGTACTGCTGCTGC | 57690 |
rs202139303 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057826 | TGTGTGTGTGTGTGT[-/GT]TGTTTTAAAGGAACG | 57690 |
rs202164617 | snp | C/T | 0.000299088 | 0.0122252 | missense | TNRC6C | GRCh38.p7 | 17:78092981 | CAGGTAAGTCCTCCA[C/T]TGATGACTCCTATGG | 57690 |
rs202206566 | snp | A/G | 0.0002918 | 0.0120754 | missense | TNRC6C | GRCh38.p7 | 17:78050185 | AGCCAGAACCCTACC[A/G]TACAGCCTGGTGGTG | 57690 |
rs202232976 | in-del | -/TA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006827 | ATTTATTTATTTATT[-/TA]TTTTTTTTTTTTTTG | 57690 |
rs202245348 | snp | A/C | | | missense | TNRC6C | GRCh38.p7 | 17:78104813 | CTAACCACCCTGCTG[A/C]CTGGGGACCTGCTCA | 57690 |
rs367657489 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078278 | TTAGCTTTGCAGAAG[C/G]GGTTCTCTCCCAGTG | 57690 |
rs367661994 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004466 | AACTTGGAACTGGAA[C/G]TGTTAGAGCTGTGTT | 57690 |
rs367669503 | snp | A/G | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109166 | GGCAGAACGGTAAAG[A/G]CAGAAAGCACAGTGC | 57690 |
rs367682145 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059377 | TCCTGTGTTTGAGGG[A/G]TTTGGTAAGTGGGGC | 57690 |
rs367690241 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081333 | GCTAGCATACGAAAA[A/G]GAGCAGGATGCACTG | 57690 |
rs367703970 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017461 | CAACCACATGGCTCT[A/G]GAGTCTGCACAGGGT | 57690 |
rs367710467 | snp | C/T | 0.000287087 | 0.0119775 | missense | TNRC6C | GRCh38.p7 | 17:78098535 | CCAGCTCCTACTCCT[C/T]GGGTAAGCTCCATGC | 57690 |
rs367722614 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062210 | GTTAGCAATTGCTGG[C/T]GATAACTGGTTAGGA | 57690 |
rs367724296 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012648 | TGTCAGTAGGTCAGT[A/G]TAAGCATTTCATGGC | 57690 |
rs367737476 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073242 | AACCACACAACAAGC[G/T]GGAACCACAGAGGGA | 57690 |
rs367775044 | snp | C/G | 0.000161987 | 0.00899817 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077196 | TCAGGATGGCGGCCT[C/G]GTGGAAGAGCCCACG | 57690 |
rs367779860 | snp | C/T | 5.14911e-05 | 0.00507375 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050064 | CCACCCCAGCCGAAG[C/T]ACCTCTAACGGTGTG | 57690 |
rs367821768 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100586 | CCCTGGGCCTGGCCC[A/G]TGAAGCCATTTTTTC | 57690 |
rs367852411 | in-del | -/TTAAC | 0.0228947 | 0.104514 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012250 | TAGTTAATTCATTAA[-/TTAAC]TTAAACAGTTAATAA | 57690 |
rs367870906 | in-del | -/TG | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105648 | AAGTGTGTGTGTGTG[-/TG]CATGTGTGGCGCGTG | 57690 |
rs367903824 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044370 | TTATTCATTCATTCA[A/T]TGTATGTTTATTTAC | 57690 |
rs367944074 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084396 | TTGCTAATGAGAGAG[G/T]ACCTCAGCCCTCAGT | 57690 |
rs367993355 | snp | C/T | 0.000126135 | 0.00794051 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104503 | CGTCCTGGGAAACAC[C/T]ACCATCCTGGCCGAG | 57690 |
rs368032653 | snp | A/C/G | 5.00215e-05 | 0.00500087 | missense | TNRC6C | GRCh38.p7 | 17:78093097 | AGTGATAAAATCTCA[A/C/G]ATGGCTCTAGCATCA | 57690 |
rs368037271 | snp | A/C/T | 3.31517e-05 | 0.00407123 | missense | TNRC6C | GRCh38.p7 | 17:78049506 | CCCAACAGGCACTTT[A/C/T]GGTGCTTGGGGAAAC | 57690 |
rs368081377 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088323 | CCTAGGTTTGAGTCC[C/T]AACTCACCACCAAGA | 57690 |
rs368083838 | snp | A/G | 0.00117481 | 0.024208 | missense | TNRC6C | GRCh38.p7 | 17:78104606 | TCCAGCAGCGCGTCC[A/G]GCCAGCCGCGGCTCA | 57690 |
rs368166090 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095431 | ATGGCATCTCCAGCC[C/T]TGAGCCTAAGAACCA | 57690 |
rs368283608 | snp | A/G | 9.97738e-05 | 0.00706236 | missense | TNRC6C | GRCh38.p7 | 17:78086549 | TGTTACAGGCCCAGC[A/G]TAATGTGTCCGGATC | 57690 |
rs368314874 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081924 | ATAATTAAAATATTT[A/G]GAGGATGAGATCTCT | 57690 |
rs368317644 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096087 | AAGCGCTGGGATTAC[A/G]TGCGTGAGCCAGTGC | 57690 |
rs368322296 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038281 | AAATACCAAGTGTTC[C/T]GACAAATCAAAAGAA | 57690 |
rs368333647 | snp | C/T | 1.8241e-05 | 0.00301996 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050691 | GGACTCGATAAGCTC[C/T]ACTGCTGTTAGTACT | 57690 |
rs368334320 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028051 | CAGGCGCCCGCCACC[A/G]TGCCCGGCTAATTTT | 57690 |
rs368338227 | snp | A/G | 0.000161987 | 0.00899818 | missense | TNRC6C | GRCh38.p7 | 17:78093035 | GTGAGTCACCAGCCA[A/G]TCCTCCCGTAGCTGT | 57690 |
rs368348935 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054337 | ACTGCAGACTACTGC[A/G]CACTACTGCAGACTA | 57690 |
rs368354900 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003756 | AATTTCAGAACCCTA[A/G]AGATCAAGTGGAAAA | 57690 |
rs368370403 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028434 | GTAGCAGTACCAAAC[A/T]GCATGTCACATGATT | 57690 |
rs368376173 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040265 | ATCATGTCAGGTTCA[C/G]TGCAGATTATGTTTT | 57690 |
rs368447395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076692 | ACAGCATGACCTCAG[C/T]AGATGTTAAAAAAAA | 57690 |
rs368461397 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071639 | GCGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 57690 |
rs368505768 | snp | A/T | 7.78422e-05 | 0.00623819 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051249 | TGATGATGGTACCTC[A/T]GCTTGGGGGGACCCA | 57690 |
rs368570801 | snp | C/T | 4.9802e-05 | 0.00498984 | missense | TNRC6C | GRCh38.p7 | 17:78049472 | CCATAGGTCAAAATA[C/T]GGGCAACCAGAACGG | 57690 |
rs368573094 | in-del | -/CC | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003171 | GTTGGACTGGTAAAA[-/CC]CAGCCAGTTCCCTAC | 57690 |
rs368636367 | snp | C/T | 1.72725e-05 | 0.0029387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098561 | CATGCTCCTCGTGTT[C/T]CGATGGGGGCCTTAC | 57690 |
rs368721740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004801 | TTAAACAGTATACCT[A/G]TTAGAGCCTGTTAAA | 57690 |
rs368756698 | in-del | -/ACAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042725 | ATGATGGTGGAGATA[-/ACAA]TGATGGTAGTGGTCA | 57690 |
rs368771834 | in-del | -/TC | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035005 | AGCAGAATGGGAAAA[-/TC]TCTGAACCATAGGTG | 57690 |
rs368786597 | snp | C/T | 0.000447484 | 0.0149513 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086460 | CATTAGTTCAACTTA[C/T]ACTTAATTATCATAC | 57690 |
rs368787679 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093192 | AGCCTGCAGAGAGTG[A/T]TTAGGCTGAGAGGAC | 57690 |
rs368796815 | snp | C/T | 0.000182541 | 0.00955181 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067842 | GGATGAAGAAGGGGA[C/T]GTGTGGAATAATGCT | 57690 |
rs368819483 | snp | C/T | 0.000155988 | 0.00883003 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079514 | GCCCAGTCTCCGTGC[C/T]CAAGTGCCTCAGTTT | 57690 |
rs368822533 | in-del | -/TGA | 0.0225045 | 0.103662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029940 | AGGTTTCATCTCCTG[-/TGA]TAACAATGACTTCTG | 57690 |
rs368827781 | snp | C/T | 0.000687717 | 0.0185307 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050376 | GTTGCCAAGGAATGA[C/T]CTTGACCCAAGAGTT | 57690 |
rs368828336 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079800 | ATTTGGCATCTTCCT[A/G]GTCAGAAGCAATATT | 57690 |
rs368830939 | snp | A/G | 0.000132738 | 0.00814564 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079371 | GCCTGCCTTGGTAAC[A/G]TGTTTAATTCTGTCC | 57690 |
rs368842347 | snp | A/G | 0.000209428 | 0.0102308 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093578 | GTGAATCAATGTGCC[A/G]GTGTTCTGATCTGTG | 57690 |
rs368872633 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060664 | TCAAACTCCTGGCCT[C/T]AAGTGATCCACCTCA | 57690 |
rs368906302 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067033 | GATGAGATACAGATT[-/T]ATGAAGCATCCCATA | 57690 |
rs368923413 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082101 | CTGGCCAGCAGCCTG[C/T]GGTGCAACAGGGCTC | 57690 |
rs368923946 | snp | A/C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097476 | TTTAAGCATTCTGGC[A/C/G]GGAATTCTCAAAGAA | 57690 |
rs368932061 | snp | A/T | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108102 | TTACAGACAGGCCTC[A/T]GAAGACAAACCGAGC | 57690 |
rs368935719 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010984 | CCGGGGGCGCCTCCC[A/G]AGGGCACTTCTCCTG | 57690 |
rs368938134 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084159 | CATGATGGCGCATGT[C/T]TGTAATCCCAGCTAT | 57690 |
rs368980267 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096214 | CGGGAGCCCAACACC[A/G]AGTTCACACAACACA | 57690 |
rs368984521 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055675 | GTCCCAATTTGAATG[C/G]CAACTCCTGGAAGAG | 57690 |
rs369004607 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099485 | TCACATGGCAGCAGA[C/T]AAGAAGAGAGAGAGA | 57690 |
rs369005272 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015969 | CTCTTAACCAGATTT[C/T]GGCTGAAGAATATAG | 57690 |
rs369017367 | snp | C/T | 5.14496e-05 | 0.0050717 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050805 | GCCCAAATCCCAACA[C/T]TGGGGAGATGGACAA | 57690 |
rs369055659 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045598 | TAGAACTCAGATTGT[A/G]GCACTATGCATGTAT | 57690 |
rs369093341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053297 | AAAGTACTTGGGGGG[A/G]TAAGGAGAAGCAGGA | 57690 |
rs369121058 | in-del | -/CCC | 0.00199481 | 0.0315187 | cds-indel, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107710 | CTTTCCAGCTCTCCA[-/CCC]CCGTGGCCCATCCAA | 57690 |
rs369166193 | snp | C/T | 0.000155988 | 0.00883003 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049056 | CTGTGGCTCAGAGAA[C/T]AGTAGCATGGCTACA | 57690 |
rs369166531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038604 | GAATGCCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 57690 |
rs369167909 | snp | C/T | 1.68049e-05 | 0.00289865 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091465 | CCCAAACATGAATGT[C/T]AACAGCATGGACATG | 57690 |
rs369184405 | snp | A/G | 0.000127119 | 0.00797141 | missense | TNRC6C | GRCh38.p7 | 17:78050729 | CTGCCAAGAGTGGCC[A/G]TGCTTGGAGTGGGGC | 57690 |
rs369196541 | snp | C/T | 6.79787e-05 | 0.00582964 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086611 | ACCCAGATTGATTTT[C/T]GTCATGAGCTATAAT | 57690 |
rs369214288 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063931 | CCATAGTTTTAAACT[A/G]TTCTTTTAAACCCTA | 57690 |
rs369221517 | snp | G/T | 0.000556431 | 0.0166705 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097792 | CTGCCTTCTTCGAGT[G/T]CCTGGCCACTCAGTG | 57690 |
rs369288549 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073417 | GTGGACACTGAGTGC[A/G]TTCCTCGTGCCTTGC | 57690 |
rs369338420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025081 | CAGGCATGAGTCACC[A/G]CGCCCGGCCAATACA | 57690 |
rs369354440 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013094 | TTAAAACTGAGCACC[A/C]TTACCAAGCTATTCT | 57690 |
rs369383786 | snp | A/C | 4.44988e-05 | 0.00471672 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071073 | TTCCCCCTTTCCCAC[A/C]CTTTGTTCAAGGGCA | 57690 |
rs369444379 | snp | A/C/G/T | 0.000184993 | 0.00961608 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091582 | CAGTGCCGCTTCCCC[A/C/G/T]CTGGAGCAGAACCCT | 57690 |
rs369473110 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088715 | AGTGATCCTGCTGGT[C/G]TCAGCTTCCCAAAGT | 57690 |
rs369485423 | snp | A/G | 0.000149033 | 0.00863099 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079463 | GACCATGCAGCAGCC[A/G]CCACAGCCACCAGTG | 57690 |
rs369498234 | snp | C/T | 3.38186e-05 | 0.00411195 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049245 | AGGCTCCAGCTCTGG[C/T]CTGGCTCACTGCTCT | 57690 |
rs369562043 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014444 | GGCATTTTCTAAATT[C/G]ATCTTCTAAATAAGC | 57690 |
rs369568283 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055170 | CTTAAAACACACATT[A/G]TACAGCTTCACAAAA | 57690 |
rs369571127 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089916 | GGCCAGTCTAGCTGA[C/T]TTTCCCAGAGGGGAA | 57690 |
rs369594505 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006108 | ATTTGAACTTCATAG[A/C]TGAACAGGAAAGGAA | 57690 |
rs369632024 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024198 | TTTAAAACACATTGA[A/G]TGGTTCTAAGTTTAC | 57690 |
rs369636161 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073915 | ATGAATCCACAAATT[G/T]AGCCTCTTTTCCATA | 57690 |
rs369636823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101220 | GTTGAAAGCTCCACA[A/G]ATCTCTAGGGCAGGG | 57690 |
rs369650967 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030847 | CTCACACCCGTAATC[C/T]CAGCACTTTAGGAGG | 57690 |
rs369661333 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051774 | TGATTCCAAGATTTC[A/G]TAACCATTTGGATAC | 57690 |
rs369666405 | snp | C/T | 6.04906e-05 | 0.00549924 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064903 | ATTTGGAAGAGCTGG[C/T]GCACCTGTTGCTGCC | 57690 |
rs369674224 | snp | G/T | 0.000163987 | 0.00905353 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098573 | GTTCCGATGGGGGCC[G/T]TACCCTTTAGGGGAT | 57690 |
rs369699104 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006988 | CTGGGGTTACAGGCA[C/T]GCATGGCCACACCCA | 57690 |
rs369705697 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035255 | TCAGCAAGCATGGAG[G/T]CAGTATGGCAAAGTG | 57690 |
rs369754441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036104 | GCCGCTGAGGGAGGC[A/G]TCCTTAGGAATTTAG | 57690 |
rs369779944 | snp | A/G/T | 5.29734e-05 | 0.0051463 | missense | TNRC6C | GRCh38.p7 | 17:78049748 | GCCTTCCTGGTGCTA[A/G/T]TGGATCATCAGTTTC | 57690 |
rs369784969 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018508 | AAATATTTTCTAAAT[A/G]AGGAGAGGATAGGTG | 57690 |
rs369803801 | snp | C/T | 0.00087848 | 0.0209396 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093791 | CTCTTCCTGCCTCTG[C/T]ATGGACGGTCTCTCT | 57690 |
rs369833231 | snp | C/G | 0.000159987 | 0.00894248 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091528 | GTCCCAGTCACGCCT[C/G]CCCCAGTGGACGCAC | 57690 |
rs369854008 | in-del | -/AG | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109294 | GTGAAGAGGGAAAAC[-/AG]AGACAGTGGGGCATC | 57690 |
rs369894779 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047088 | GTCTTAGTCAAGAGG[A/C]AGCCTGCCTTATGGC | 57690 |
rs369940560 | snp | A/C | 1.72907e-05 | 0.00294025 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092926 | TTGTTTCCTATTGTC[A/C]CCATAGGTGCTATCC | 57690 |
rs369950657 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78041015 | TCGCTGTACCCAGCC[A/G]ACATGTTGTAGCGAG | 57690 |
rs369953147 | snp | C/T | 0.000234935 | 0.0108357 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067899 | CAGCTCCTGGGGGAA[C/T]GCCCCCAAAAAAGGA | 57690 |
rs369955761 | snp | A/C/G | 9.97198e-05 | 0.00706052 | missense | TNRC6C | GRCh38.p7 | 17:78049646 | TGAACTCTTCACCCA[A/C/G]CCCTATCAATGCAAT | 57690 |
rs369974427 | snp | C/T | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031824 | GGAACACAGCATCAT[C/T]CCAGTAAGCTCCAAC | 57690 |
rs369991763 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066449 | TACTTTTTTTTACAA[A/G]CCTAAAGGATAAGGG | 57690 |
rs370001052 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070878 | AATTGCACATATATA[C/G]CAACCTGCAAATGTA | 57690 |
rs370014862 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009268 | TTGGCACTGCCCTTA[A/T]TTGAGGCACAGGTAA | 57690 |
rs370052034 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083581 | CAGTTGAGCTCTCAG[C/G]CAGAGTTTCTGAGAA | 57690 |
rs370052385 | snp | A/G/T | 0.000133018 | 0.00815437 | missense | TNRC6C | GRCh38.p7 | 17:78087093 | GCTCCTTACCCTCTC[A/G/T]GTGAGTGTCCCATGG | 57690 |
rs370060606 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086688 | TTGATTTTTCTCTAG[A/C]CAAGCCTTCCTTTGA | 57690 |
rs370062894 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062401 | TAGTCAGAAAATTAA[A/T]ACATTTTGTAATTGA | 57690 |
rs370148948 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100824 | CTTGTCACCCAGGCC[A/G]GAGTACAGTGGCGTG | 57690 |
rs370169438 | snp | C/G | 3.31757e-05 | 0.00407269 | missense | TNRC6C | GRCh38.p7 | 17:78049895 | TGAACTCAGCATTAA[C/G]TGCTAAACAAAATGG | 57690 |
rs370182394 | snp | A/C/T | 0.000269423 | 0.011604 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78071159 | ACTCACAGACATGGG[A/C/T]TTCCCGGTAACTGGC | 57690 |
rs370201986 | snp | A/G | 7.41468e-05 | 0.00608834 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098365 | GTCAGACATCAAATC[A/G]ACGTGGTCCTCTGGC | 57690 |
rs370272710 | snp | A/C | 0.000159987 | 0.00894248 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083177 | AGCTGGTGAGTGGAT[A/C]GACCCATGCAAGTTA | 57690 |
rs370277713 | snp | A/G | 5.38914e-05 | 0.00519065 | missense | TNRC6C | GRCh38.p7 | 17:78050620 | GCCGCTGTGCCAGCA[A/G]ACACAGGTTGGGGAG | 57690 |
rs370283085 | snp | G/T | 6.67579e-05 | 0.00577707 | missense | TNRC6C | GRCh38.p7 | 17:78104513 | AACACTACCATCCTG[G/T]CCGAGTTCGCTGGTG | 57690 |
rs370306183 | snp | C/T | 6.15025e-05 | 0.00554504 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051201 | TGGCTGGGAAGAACC[C/T]TCTCCACCGTCCATT | 57690 |
rs370339386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045487 | GAAGGTCTGAGTAGG[C/T]GGCGTCATTGTAGTG | 57690 |
rs370345459 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014185 | TGAGATTTAGGATTT[A/G/T]CCATTTGTTCTGAGA | 57690 |
rs370353891 | in-del | -/CTGCAGCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090513 | AGGGGAACTGCAGCT[-/CTGCAGCT]GGAAATACAAGGGGA | 57690 |
rs370401770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054117 | TAGGCAGTTGTAGGA[C/T]GATGGTAAGTATTTA | 57690 |
rs370403402 | snp | C/G | 6.63317e-05 | 0.0057586 | missense | TNRC6C | GRCh38.p7 | 17:78086973 | CACCTGTCTCTGCAC[C/G]CCTCTGCAGGCAAAT | 57690 |
rs370409606 | snp | C/T | 0.000159987 | 0.00894248 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075161 | GGAAAAGAAGGTGGA[C/T]GTGGACAAGCGTGGG | 57690 |
rs370411706 | in-del | -/AT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021998 | AGTAGTTGGAACTCT[-/AT]TAGTATCTGGCTCTT | 57690 |
rs370412691 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087349 | TCTTGAACTCCTGGG[A/C]TCAAGCAATCCTCCC | 57690 |
rs370424563 | snp | C/T | 5.03478e-05 | 0.00501711 | missense | TNRC6C | GRCh38.p7 | 17:78049283 | GTGGGGATGGAAAAA[C/T]GGACACTATGATTGG | 57690 |
rs370443868 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027490 | ATCATATGGAAACTC[C/T]GGCTAGAAAAAAAAC | 57690 |
rs370445459 | snp | A/G | 0.00129766 | 0.0254391 | missense | TNRC6C | GRCh38.p7 | 17:78051142 | GGAACAGGGTGGATC[A/G]GGGGGCCGGTACCGG | 57690 |
rs370486959 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018136 | TTGTTTTGTTTTTTT[-/T]GGTTTTTTTGAGATG | 57690 |
rs370534213 | snp | C/T | 0.000165986 | 0.00910855 | missense | TNRC6C | GRCh38.p7 | 17:78092963 | GTCTAAGCATTGGGC[C/T]TCCAGGTAAGTCCTC | 57690 |
rs370549877 | snp | C/T | 5.00597e-05 | 0.00500273 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098512 | GGGTGCCAGCCCCCT[C/T]GGCTGGACCAGCTCC | 57690 |
rs370565699 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107160 | ACTTCCCGTGCTGCC[A/G]GCGAGCATTGAGTTG | 57690 |
rs370584226 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003332 | GAGAGTATCTAAGGG[A/G]AGAGGCATCCAGAGA | 57690 |
rs370594640 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090135 | GGTCTGCGAAGTGTG[C/T]GTGTGCATGTGCATA | 57690 |
rs370602371 | snp | A/C/T | 0.000183394 | 0.00957422 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103599 | CAAGTAGCTCCCCAT[A/C/T]CCCCAGAGCATTAGG | 57690 |
rs370632434 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033651 | TCCAGCCTGGGTGAC[-/AA]GAGTGAAACTCCGTT | 57690 |
rs370654504 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058314 | CAGATCCTAAAAATA[C/T]TCAGCAACATGATTA | 57690 |
rs370748045 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031739 | ATTGCCTACGGGGAC[C/T]CTAACCAGTGTGAGC | 57690 |
rs370753226 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048404 | GCCATGTTTCGCCTC[C/T]ATATAATACTGTAAC | 57690 |
rs370759256 | in-del | -/AT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029837 | CACACACACACACAC[-/AT]AAGCCAAGGCCTACA | 57690 |
rs370777558 | snp | C/T | 0.000316016 | 0.0125662 | missense | TNRC6C | GRCh38.p7 | 17:78086947 | AGCCACCACCGCCAC[C/T]GCCCCCGCCGCACCT | 57690 |
rs370842014 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010812 | CATGGAAACAAAAAA[A/G]ATATTAAGATGAGAC | 57690 |
rs370846027 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047174 | TGCTGGCAACAAGCC[A/G]TAATCTCTGTGTGTT | 57690 |
rs370855007 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080228 | GAGGTGGGTGGATCA[C/G]CTGAGGTCAGGAGTT | 57690 |
rs370902395 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083999 | AGAAAATGACCAGGA[A/G]TCGGCCGGGCACGGT | 57690 |
rs370913980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038961 | GCTGTTGGTCGGAAT[A/G]TAAGGAGGCATGTGG | 57690 |
rs370935435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071216 | CTTCCCAAAATGAAA[C/T]GCCCTCATTGTTTCC | 57690 |
rs370940947 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037616 | AAGCGCAGACCCGCA[A/G]TTGTAAAGCCTCTCA | 57690 |
rs371027036 | snp | A/G | 1.65985e-05 | 0.00288079 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050487 | GAAAAATGACAATGG[A/G]ACAGAGGCCTGGGGT | 57690 |
rs371033415 | snp | C/T | 0.000351386 | 0.0132503 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102581 | TCACTGAGCATGATC[C/T]AGGGAGGGTTCCCGC | 57690 |
rs371048350 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083607 | GAGAACCACAGAACA[C/G]AAAAAATCATTTGAG | 57690 |
rs371164154 | snp | A/G | 1.79142e-05 | 0.00299279 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050145 | TGGGAAAGGATCAAC[A/G]GGGTGGGAGAGTCCT | 57690 |
rs371176504 | snp | A/G | 3.31658e-05 | 0.00407208 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077211 | CGTGGAAGAGCCCAC[A/G]CCTTCACCGTTCTTG | 57690 |
rs371186463 | snp | A/G | 0.000135137 | 0.00821891 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098536 | CAGCTCCTACTCCTC[A/G]GGTAAGCTCCATGCT | 57690 |
rs371196010 | in-del | -/TTGTTG | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109129 | TTGTTGTTGTTGTTG[-/TTGTTG]CTGCTATTTTGGCAA | 57690 |
rs371253551 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033419 | TCACGCCTGTAATCC[A/C]AGCACTTTGGGAAGC | 57690 |
rs371335834 | snp | C/T | 0.000163987 | 0.00905352 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049992 | TCCTGGAATACTCGC[C/T]TGGGGAAGGGGCAGT | 57690 |
rs371363782 | in-del | -/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106882 | TCAAAACAAAAAAAA[-/T]ACAAAAAAAAAAAAA | 57690 |
rs371395153 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080993 | GCTGTAACAAAATAC[C/T]TTAGACTGGGTCATT | 57690 |
rs371395192 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013509 | TATTGAGCACCTGCT[A/G]TTTGCTTGGTACTGT | 57690 |
rs371416574 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043752 | CACTACCCTTCCTAG[A/C]CTCTATCTTCATAAG | 57690 |
rs371424345 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022939 | CAGTATAACAGCTAT[C/T]TATATAGCATGTAAA | 57690 |
rs371444681 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061701 | TATTAAATAAATATC[A/G]AAATGGAAATATTTG | 57690 |
rs371446050 | snp | C/T | 0.0010479 | 0.0228659 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079584 | GCAACAGGATATAGA[C/T]GCCAGTGTTTCGTGG | 57690 |
rs371451302 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066139 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 57690 |
rs371469493 | snp | C/G | 4.97113e-05 | 0.00498529 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049527 | TTGGGGAAACTTGCT[C/G]CCACAAGAGAGCACA | 57690 |
rs371471133 | snp | A/G | 0.000161987 | 0.00899817 | missense | TNRC6C | GRCh38.p7 | 17:78067855 | GACGTGTGGAATAAT[A/G]CTGCTTCCCAAGAAA | 57690 |
rs371483285 | in-del | -/AAGTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057144 | TGCTGAAAGTATGTT[-/AAGTT]TAGTATATTGTACAA | 57690 |
rs371535788 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073247 | CACAACAAGCTGGAA[C/G]CACAGAGGGAGCCTC | 57690 |
rs371558403 | in-del | -/ATC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060466 | CATTTTTAATCGTTT[-/ATC]TTTTTTTTTTTTTTT | 57690 |
rs371574239 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021980 | TGATAGTCTAATATT[A/G]CAAGTAGTTGGAACT | 57690 |
rs371633424 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081646 | CCACTTCCCAGGAAC[A/G]GGGGAAAAGGCAGCA | 57690 |
rs371647477 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004074 | CTGTATACCATATGC[A/G]AAATTCTGACTTAAG | 57690 |
rs371681337 | in-del | -/TG | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107185 | GAGTTGTAGAAAAAC[-/TG]TTGTTTTAAAATTGG | 57690 |
rs371686758 | snp | A/T | 0.000163986 | 0.00905352 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064819 | GGTGGATAATGGCAC[A/T]GCAGCATGGGGGAAG | 57690 |
rs371696613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103766 | CCTTGGCTGTAGACA[A/G]CTGCCTTCTCCCTCT | 57690 |
rs371705492 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017229 | AAATGTCTTAAATAT[C/T]TCTAAATAAATTTTT | 57690 |
rs371710039 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100178 | GCAAGCTGTCAGTGG[A/C]TCTACCATTCTGGGG | 57690 |
rs371794914 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028590 | TGGTAGTGTGGACAA[C/T]GTAGCGTTCACATGG | 57690 |
rs371818857 | snp | A/G/T | 0.000154604 | 0.00879091 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098556 | AGCTCCATGCTCCTC[A/G/T]TGTTCCGATGGGGGC | 57690 |
rs371825660 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042475 | AATACTTCAAACTCC[A/G]AAATGGTATAAAGTA | 57690 |
rs371837976 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018856 | AGAGAAGCTGGATGG[C/T]ATCAGGATTCCAGAG | 57690 |
rs371841825 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067210 | AATTAGCTGGATGTG[A/G]TGGCACATGCCTGTA | 57690 |
rs371842605 | in-del | -/TT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042580 | ATTTTTTTTTTTTTT[-/TT]AACGAAATTTAACCT | 57690 |
rs371845442 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084074 | GGATCACCTGAGGTC[A/T]GGAGTTCGAGATTAG | 57690 |
rs371862549 | snp | A/G | 9.96049e-05 | 0.00705638 | missense | TNRC6C | GRCh38.p7 | 17:78049475 | TAGGTCAAAATATGG[A/G]CAACCAGAACGGGAA | 57690 |
rs371862754 | snp | A/G | 8.29869e-05 | 0.00644101 | missense | TNRC6C | GRCh38.p7 | 17:78093043 | CCAGCCAGTCCTCCC[A/G]TAGCTGTTCCCCATA | 57690 |
rs371932308 | snp | A/G | 3.58192e-05 | 0.00423182 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093169 | GCAGCAGGTCAGAAT[A/G]TGCTCCAAGCCTGCA | 57690 |
rs371994763 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106537 | TAAAAAAAAAAAAAA[-/C]AAAACAAAACAAAAA | 57690 |
rs372002004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088274 | AGAGCCCTTTGTGTC[A/G]AAGTAGGTAAGACCT | 57690 |
rs372008818 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089022 | GCCCAGGCTGGAGTG[C/T]GATGGCGCAGTCTCG | 57690 |
rs372047679 | snp | A/G/T | 0.000222128 | 0.0105367 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78049018 | GCCTCAGAATGTACT[A/G/T]CAGACACTGACTCTG | 57690 |
rs372077559 | snp | A/G | 4.968e-05 | 0.00498373 | missense | TNRC6C | GRCh38.p7 | 17:78079426 | TGGGTATGTTTGGCA[A/G]TAGTGGAGCAGCACA | 57690 |
rs372081507 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078314 | CAGGCGGCTGTTCCC[A/G]AGTGAAGCTGTGCAA | 57690 |
rs372093428 | snp | C/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109265 | CATCATGGCGAGCCC[C/T]GACTGAGTGTTCAGT | 57690 |
rs372097448 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069538 | ACAGGTGCATGCCAC[C/T]CTGCCCAACTAATTT | 57690 |
rs372104877 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084337 | AGAAAAAAAAAAAAA[A/G]AAGAATGGGAACTCC | 57690 |
rs372149000 | in-del | -/TTA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014590 | TGTTTGTAGTCATTA[-/TTA]AAATAATTTTGCTTT | 57690 |
rs372162944 | snp | C/T | 1.77461e-05 | 0.00297871 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091418 | AGGAGCAGGCGAATC[C/T]TAACCGCATCTCTCT | 57690 |
rs372229608 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096102 | ATGCGTGAGCCAGTG[C/T]GCACGGCCGAGCTGA | 57690 |
rs372230584 | snp | A/G | 0.000218203 | 0.0104429 | missense | TNRC6C | GRCh38.p7 | 17:78050015 | GGGGCAGTGGCAACA[A/G]TGGCGTTGGTAATAT | 57690 |
rs372236223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084217 | TGAACCTGGAAGGCG[G/T]AGGTTGCAGTGAGCC | 57690 |
rs372242948 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017909 | ACCCTGACATACTTT[C/T]TCAGGCTCTGCTTAA | 57690 |
rs372252157 | snp | A/G | 0.000109407 | 0.00739538 | missense | TNRC6C | GRCh38.p7 | 17:78050698 | ATAAGCTCTACTGCT[A/G]TTAGTACTGCTGCTG | 57690 |
rs372252994 | snp | C/T | 3.6361e-05 | 0.0042637 | missense | TNRC6C | GRCh38.p7 | 17:78050653 | AGCAACAACAAAGCG[C/T]CAAGTGGCCCGGGGG | 57690 |
rs372257288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081994 | TCTTTCTTATTCTTT[A/G]CGTGCTAACTACTAA | 57690 |
rs372277985 | snp | C/T | 5.19566e-05 | 0.00509663 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067939 | GTAAGTACAACACTC[C/T]TAACGACGGTACACC | 57690 |
rs372282181 | snp | C/T | 3.48858e-05 | 0.00417632 | missense | TNRC6C | GRCh38.p7 | 17:78049720 | GGGGCCATCATCCCG[C/T]CCCACCTGCAAGGCC | 57690 |
rs372290004 | snp | C/T | 3.31318e-05 | 0.00406999 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093741 | CATCCAGGATGTCAA[C/T]CGCTACCTCCTCAAG | 57690 |
rs372330041 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008462 | TGATCATGGGAACCA[C/T]GTTTTCTCTGCAGCC | 57690 |
rs372355325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023300 | CTGTACTTTGACTTT[C/T]ATAGTAGCTAGCCAT | 57690 |
rs372356057 | snp | C/T | 0.013751 | 0.0817703 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104856 | TGTAGGCTCTGCCAT[C/T]ATCAGCACCAGGAGA | 57690 |
rs372357863 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040778 | AAGAGGAAGGAAGAT[C/G]GGTTTAGTGTCAGCT | 57690 |
rs372415110 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016150 | AGGAATAATTGAGAG[G/T]CCCTATTGGCTCTCT | 57690 |
rs372425874 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071892 | AGTTTCCAGTCATAC[A/G]TAGGGAGAATTCATA | 57690 |
rs372444751 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058113 | TGACACTCCTCGAAC[A/C]TTGCCTCAATTACTC | 57690 |
rs372498870 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064066 | TTTCATGTTTTGAGA[C/G]AGATTCTTGCTCTGT | 57690 |
rs372519837 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038431 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 57690 |
rs372523998 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024206 | ACATTGAGTGGTTCT[A/G]AGTTTACCAGACAAG | 57690 |
rs372527086 | snp | A/G | 0.00281497 | 0.0374107 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098563 | TGCTCCTCGTGTTCC[A/G]ATGGGGGCCTTACCC | 57690 |
rs372543039 | snp | C/T | 3.38639e-05 | 0.0041147 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087141 | AGGTAGAGAGGGTAC[C/T]TGGAGTCCGTATGTG | 57690 |
rs372550078 | snp | C/T | 0.000165986 | 0.00910854 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051276 | CCCAAGCAACTATAA[C/T]AATAAAACTGTAAAC | 57690 |
rs372583885 | snp | C/T | 3.31917e-05 | 0.00407367 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050418 | TGGTTGGGGACAGAC[C/T]CCTGTAAAGCAAAAC | 57690 |
rs372595894 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106747 | CAAGGAAGAAAGACA[A/G]TGGAATAACATACCT | 57690 |
rs372596080 | snp | A/G | 3.64186e-05 | 0.00426708 | missense | TNRC6C | GRCh38.p7 | 17:78050258 | CAGCAAGTGAAGGAA[A/G]TAGTGATGGTTCTGG | 57690 |
rs372710367 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107391 | TTGAAGAACATGCAT[C/T]GAAAGTTGCTTTCGA | 57690 |
rs372814490 | snp | A/C | 0.0150606 | 0.0854603 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106532 | TTATTTAAAAAAAAA[A/C]AAAACAAAACAAAAC | 57690 |
rs372831568 | in-del | -/AT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063249 | GACTCTGTCTCCAAA[-/AT]ATATATATATATATA | 57690 |
rs372835174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018288 | TGCATCACCACGCCC[A/G]TCTAACTTTTGTATT | 57690 |
rs372840738 | snp | A/G | 3.36355e-05 | 0.00410081 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086505 | GTTCTGTCAACAGGC[A/G]TACCAACGTTTACAA | 57690 |
rs372874993 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043060 | TTCAGTAAAATTAAT[C/T]TGTGAAGAGCCAGAT | 57690 |
rs372877854 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080044 | ATAGTGTATATATTA[C/T]AGATTTTCAGTTATG | 57690 |
rs372894604 | snp | A/C | 1.65979e-05 | 0.00288074 | missense | TNRC6C | GRCh38.p7 | 17:78098493 | CCAAGCCCTCCTCCA[A/C]CTGGGGTGCCAGCCC | 57690 |
rs372912091 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100137 | TCACGGGCTGGTATT[A/G]TCTGCAGCTTTTCCA | 57690 |
rs372931007 | snp | G/T | 5.27607e-05 | 0.00513591 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067709 | AGTGGAAGCATTGTC[G/T]GCGTTAGGGACATGA | 57690 |
rs372976735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045650 | ATATATTGTTTGCCT[A/G]TATGTGGCAAGCATT | 57690 |
rs372995112 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082782 | CTGACTGCACATCCA[-/T]TTATAGGCTCTCTGC | 57690 |
rs373024928 | snp | C/G/T | 3.52829e-05 | 0.00420005 | missense | TNRC6C | GRCh38.p7 | 17:78049774 | GTTTCTCAAGTCAGT[C/G/T]GGGGCAGTGCTGAAG | 57690 |
rs373105504 | snp | A/C/G | 0.000101349 | 0.00711802 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086948 | GCCACCACCGCCACC[A/C/G]CCCCCGCCGCACCTG | 57690 |
rs373111046 | snp | A/C | 4.45732e-05 | 0.00472066 | missense | TNRC6C | GRCh38.p7 | 17:78051055 | AAACCTGGCCCCCAA[A/C]AGAACTGGGCTAGCA | 57690 |
rs373112227 | snp | A/G | 6.63581e-05 | 0.00575974 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093798 | TGCCTCTGCATGGAC[A/G]GTCTCTCTAGACCCA | 57690 |
rs373177147 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047304 | TGTCATAAACCAGGG[G/T]TATAGAGCCAACCCC | 57690 |
rs373184901 | snp | C/T | 1.65729e-05 | 0.00287857 | missense | TNRC6C | GRCh38.p7 | 17:78079536 | CCTCAGTTTCTATCC[C/T]CTCAGGTCAGACCCA | 57690 |
rs373219076 | snp | C/T | 8.96338e-05 | 0.00669394 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064881 | ACCCTGCAGAGCCGC[C/T]GGTGGCATTTGGAAG | 57690 |
rs373249139 | snp | C/T | 0.000257336 | 0.0113403 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083018 | TTAACAGAGATACAA[C/T]GGCTAATAGTATATT | 57690 |
rs373292463 | snp | C/T | 0.000441209 | 0.0148462 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104849 | GAGTCCCTGTAGGCT[C/T]TGCCATCATCAGCAC | 57690 |
rs373328884 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075640 | TGTTAGATGTTTATC[C/G]TCAGGAAAAGGGATT | 57690 |
rs373354032 | snp | C/G | 0.000384857 | 0.0138665 | missense | TNRC6C | GRCh38.p7 | 17:78091595 | CCCCTGGAGCAGAAC[C/G]CTAGCAAGCATGGTA | 57690 |
rs373366541 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78041046 | AGGCCAGGCGAGCCT[C/G]GATGCAGGCGTAGAG | 57690 |
rs373368572 | snp | C/G | 6.69669e-05 | 0.0057861 | missense | TNRC6C | GRCh38.p7 | 17:78049845 | TGCCACAGGAAATAG[C/G]AATTCTGGGTTCAGT | 57690 |
rs373374029 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019094 | TAGTGAAAGGAAGGA[A/G]GGTCGGGGGCCTCGG | 57690 |
rs373383821 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019396 | TTTGTGTCCATACTG[C/T]AGCCTGTCATTTTAG | 57690 |
rs373389276 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066912 | ACTTAATGCTCATAG[A/G]TTTGGATCAAGCAGT | 57690 |
rs373391561 | snp | A/G | 0.000278154 | 0.0117898 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78071096 | CAAGGGCATGAAGAC[A/G]TCTGGCAAGCAGGAT | 57690 |
rs373425606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024027 | AGGCAGGAGAATCAC[A/T]TGAACCCAGGAGGCA | 57690 |
rs373428671 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060209 | ATGAGCAAACTCTTC[C/T]ATATAAAGTTTCATT | 57690 |
rs373442015 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105060 | ATGACAGGATGTTCC[C/T]CGTAGCTTTTTATTT | 57690 |
rs373495039 | in-del | -/TACA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062010 | ATTTAATTACCTACA[-/TACA]GTAAATTAGTATTTT | 57690 |
rs373517056 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020362 | TTGTGGCATTTTTTT[-/T]CTGTTTGTAAAATAA | 57690 |
rs373554023 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068182 | CTTTATTGTAGCAGA[C/G]AATGTGCAGAAACAG | 57690 |
rs373605701 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030160 | TAGACTTTTTTTTTT[-/T]GTTTTTGGAGACGGA | 57690 |
rs373611929 | snp | C/T | 5.56839e-05 | 0.00527626 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071038 | TCTGGTAGAAATGCA[C/T]TAAAATGTAGCTCAT | 57690 |
rs373661067 | snp | A/G | 0.000177984 | 0.00943188 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104797 | AGGCAGCCCCACGCC[A/G]CTAACCACCCTGCTG | 57690 |
rs373687623 | snp | C/G/T | 1.81122e-05 | 0.00300928 | missense, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050640 | AGGTTGGGGAGACAG[C/G/T]AACAACAAAGCGCCA | 57690 |
rs373731306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080273 | CCAATATGGCGAAAC[A/C]CCATCTCTACTAAAA | 57690 |
rs373731370 | in-del | -/TCATGACCAGGAATCATGAAGGAG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084300 | AAAAAAAAAAGAAAA[-/TCATGACCAGGAATCATGAAGGAG]AAAAAAAAAAAAAAA | 57690 |
rs373774035 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097669 | GTTGATTCCTGATGG[C/T]TCTCACACCCCACAG | 57690 |
rs373812857 | snp | C/T | 0.000558815 | 0.0167061 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103385 | AATCAGAAGAAAGCT[C/T]ATTCATGTCCCTGTG | 57690 |
rs373843245 | snp | C/G | 1.73685e-05 | 0.00294685 | missense | TNRC6C | GRCh38.p7 | 17:78050347 | AAAGGGATTATAGAC[C/G]AAGGGCACATCCAGT | 57690 |
rs373862985 | snp | A/G | 1.65603e-05 | 0.00287747 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079478 | GCCACAGCCACCAGT[A/G]CAGCCTCTTAACTCT | 57690 |
rs373871416 | snp | A/G | 0.000157988 | 0.00888644 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086990 | CTCTGCAGGCAAATC[A/G]GCCATGGACAGCTTC | 57690 |
rs373876825 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070675 | CTCATTGGAATAAAC[A/C/G]CCCTCATTTTATCAT | 57690 |
rs373894014 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044687 | TGGAAATAAAGTTTT[G/T]TTGGCACACAGCCAC | 57690 |
rs373894465 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031896 | AAACTTTGCTATTTT[C/G]AACTTTGCTGCTGAG | 57690 |
rs373920317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026301 | GCTGTGCCAAATACC[A/G]GGTACTGTGGATGTT | 57690 |
rs373922897 | snp | A/G | 8.84408e-05 | 0.00664925 | missense | TNRC6C | GRCh38.p7 | 17:78075193 | TGGGAGTGACCGACC[A/G]TAATGGAATGGCCGC | 57690 |
rs373925530 | snp | G/T | 3.39242e-05 | 0.00411837 | missense | TNRC6C | GRCh38.p7 | 17:78050041 | AATATCCATTCAGGA[G/T]CTTGGGGCCACCCCA | 57690 |
rs373926211 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089246 | GTGTTGGGATTACAG[A/G]CGTGAGCCACCGTGC | 57690 |
rs373937507 | snp | C/G | 0.000163987 | 0.00905353 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098521 | CCCCCTCGGCTGGAC[C/G]AGCTCCTACTCCTCG | 57690 |
rs373949733 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060435 | AGCAAGCACTCAATA[A/T]ATGCCTGATCGATTG | 57690 |
rs373950316 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005714 | CACCCACTCAGGAGT[C/T]ACATAAACTAGCTCT | 57690 |
rs373951852 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055208 | TTATATTCTTATTCT[A/G]TGAGCTTTTTTTTTG | 57690 |
rs373986140 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016361 | CATGTAACTGGGGGA[A/G]CCAGATCCCTAGCCT | 57690 |
rs373987764 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048419 | TATATAATACTGTAA[A/C]CTAATTAGAGGTCTT | 57690 |
rs373990619 | snp | C/G | 0.000157988 | 0.00888644 | missense | TNRC6C | GRCh38.p7 | 17:78086906 | GCAGCACCAGCGCCA[C/G]CTGGCCCAGGCCCTG | 57690 |
rs373991520 | snp | C/T | 0.00199529 | 0.0315338 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039317 | AAATCTTGCCCCCCC[C/T]CCCCACTCCCTACCT | 57690 |
rs374006694 | snp | A/G | 0.000163987 | 0.00905353 | missense | TNRC6C | GRCh38.p7 | 17:78067790 | AAGGCTGGGGCAGTG[A/G]TGGGGATGAAATGAA | 57690 |
rs374020211 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009751 | ATAGAGACAGGGTTT[C/T]ACCATGTTTGCCAGG | 57690 |
rs374030534 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033183 | TTGTGATGTGATTGG[C/T]TGACAGTATTGCATC | 57690 |
rs374030683 | snp | A/G | 5.28658e-05 | 0.00514102 | missense | TNRC6C | GRCh38.p7 | 17:78050596 | TCTGGGTGGGTCAAC[A/G]CGCCACCTGCCGCTG | 57690 |
rs374047816 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101873 | ACCTTCCAGCATGGG[C/T]GTCATGGCCATCATG | 57690 |
rs374066018 | snp | C/T | 0.000221845 | 0.0105296 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086829 | TTCCCACCTAGTTAA[C/T]GCACCTATGTCTCTG | 57690 |
rs374073988 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082859 | CTTGCATTGTCTTTA[C/G]ACAGTCCTGCATGCA | 57690 |
rs374156938 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027696 | GTGAGACATATCGGT[A/G]TTGCACATACCATTA | 57690 |
rs374191467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075356 | GTGTCCTTAATACAA[A/G]CCAGATTAAAAACTT | 57690 |
rs374238087 | snp | C/T | 1.6715e-05 | 0.00289089 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083209 | AGCACGCAGGCCGAG[C/T]GCAGATGCACGGCAC | 57690 |
rs374242584 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043400 | GCATTGTTCCAAATT[A/G]ACTTCTATAGTAAAA | 57690 |
rs374242888 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084642 | TTTTTTTTTTTGAGA[C/T]GGCGTCTTGCTAGTC | 57690 |
rs374271464 | snp | A/G | 1.67063e-05 | 0.00289014 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050001 | ACTCGCCTGGGGAAG[A/G]GGCAGTGGCAACAAT | 57690 |
rs374373797 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033598 | CGCTTGAACCTGGGA[C/G]GTGGAGGTTGCGGCG | 57690 |
rs374469699 | snp | G/T | 4.34641e-05 | 0.00466156 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077278 | GCACTCCCCAGTCAG[G/T]CCCTGGGTGGGATTG | 57690 |
rs374485909 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065705 | ACAGAATTCCACTGG[A/G]TGGAATTTGCCATGT | 57690 |
rs374490552 | snp | C/T | 6.8278e-05 | 0.00584246 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098383 | GTGGTCCTCTGGCCC[C/T]ACCTCCCACACGCAA | 57690 |
rs374510417 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028142 | CCTTGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 57690 |
rs374543749 | in-del | -/GT | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108494 | CTACAGGGGCAAACT[-/GT]ACCCGTGCCTGTGCG | 57690 |
rs374555931 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096640 | GGCTTTTCAGAAACC[A/G]TCCGATTCTGTTTAT | 57690 |
rs374564328 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067556 | TAGCTGATGTTTGAA[A/G]GAAAAATTATATACA | 57690 |
rs374583388 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097943 | GCCCCAGCTTTTCCT[A/C/G]TTGGCTCTTTACTCA | 57690 |
rs374625321 | in-del | -/TTAG | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047239 | GGCTTATTTATCTCT[-/TTAG]TTAGTTATTATATTA | 57690 |
rs374635280 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041239 | TGTGAGTGGTAGCCC[A/G]GCGTCCCTAAGCTCT | 57690 |
rs374641568 | snp | A/T | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049140 | TGGCACCAATGGCGC[A/T]CTCGTCCAAAGCCCT | 57690 |
rs374674774 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076624 | TAAAATATGGAATAA[C/T]GCACAGGCTGGTTGT | 57690 |
rs374701318 | snp | C/T | 9.95801e-05 | 0.0070555 | missense | TNRC6C | GRCh38.p7 | 17:78067861 | TGGAATAATGCTGCT[C/T]CCCAAGAAAGCACCT | 57690 |
rs374792685 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084234 | GGTTGCAGTGAGCCT[C/T]GCACCTTTGCACTCC | 57690 |
rs374814954 | snp | A/G | 3.34448e-05 | 0.00408917 | missense | TNRC6C | GRCh38.p7 | 17:78049297 | ATGGACACTATGATT[A/G]GAGATGGGAGAAGTC | 57690 |
rs374816234 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060359 | TTTAAAGGCCGTTGG[C/T]ATGAGTAAAAAATCT | 57690 |
rs374825114 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079382 | TAACGTGTTTAATTC[C/T]GTCCCTGTGCAGATA | 57690 |
rs374827456 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093415 | ACCCTGTGTGAAAAC[A/T]AGCTTAATATGATAG | 57690 |
rs374830447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037846 | GAAGAGCGAATGTAC[A/G]TGAATAGAAGAGCCA | 57690 |
rs374835057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064521 | CATCTCTAAATAAAA[A/G]TAAATGAATAAAAAT | 57690 |
rs374842943 | snp | C/G | 0.000103407 | 0.00718978 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067749 | GTTCATGTTTGCTCT[C/G]TTTCTAGCTTCAAAA | 57690 |
rs374885554 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045888 | TAGAGATTTAACATA[A/G]TATCATGCCATATTT | 57690 |
rs374942048 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038402 | CTTGTGGCTGGGTGC[A/G]GTGGCTCACGCATGT | 57690 |
rs374957323 | in-del | -/TTTG | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107260 | GGGTTTGAGGGGTTT[-/TTTG]TTTGTTTGTTTTTTG | 57690 |
rs374963738 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059241 | GACCTCTGCAGCCAG[A/G]AGTAATTCTATTTTA | 57690 |
rs374979639 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094659 | TTGCCAGGCTGATCT[C/T]GAACTCCTGACCTCA | 57690 |
rs374985368 | in-del | -/TCAC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056854 | TAAAAGGGCCAAAAT[-/TCAC]AATTCTCTTTTATAT | 57690 |
rs375075512 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099437 | TGTGTCTGGGGAGGC[C/T]TCACAATCCTGGTAG | 57690 |
rs375078467 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015543 | TTTTAACAGTAAATG[C/T]CATTACTGGGAAACA | 57690 |
rs375134490 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018220 | CAACCTCCACCTCCC[A/G]GGCTCAAGTGATTCT | 57690 |
rs375169048 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071223 | AAATGAAATGCCCTC[A/G]TTGTTTCCTCTCCAT | 57690 |
rs375224005 | in-del | -/AAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018043 | AATCATTTTAAAGAT[-/AAT]GTCTCTTCTACTATA | 57690 |
rs375277687 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045499 | AGGCGGCGTCATTGT[A/G]GTGGAAGTGGTTCCC | 57690 |
rs375279403 | snp | A/C | 1.65798e-05 | 0.00287917 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093788 | CTGCTCTTCCTGCCT[A/C]TGCATGGACGGTCTC | 57690 |
rs375339809 | snp | C/T | 7.01041e-05 | 0.00592006 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067951 | CTCTTAACGACGGTA[C/T]ACCCTGAAAACCAAA | 57690 |
rs375391262 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070909 | CCTTGATGCTTTCCG[C/T]AGCAGTAGCCACGAA | 57690 |
rs375414163 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072363 | TTAGAGAAAAGTTGT[C/T]GATGGTGGAGCCTAG | 57690 |
rs375458850 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018874 | CAGGATTCCAGAGTG[C/T]AGGAAAAGTTTTAAG | 57690 |
rs375475614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021686 | GTCATTATTCTGCCT[C/T]AGCCTCCCAAGTAGC | 57690 |
rs375485878 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042129 | GTAATCCTTTTTAAT[G/T]TAATCACTTAAGACA | 57690 |
rs375511234 | snp | A/G | 3.4706e-05 | 0.00416555 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098567 | CCTCGTGTTCCGATG[A/G]GGGCCTTACCCTTTA | 57690 |
rs375537494 | snp | C/T | 1.65949e-05 | 0.00288048 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049914 | TAAACAAAATGGATC[C/T]AGCAGTGCTGTGCAA | 57690 |
rs375541821 | snp | C/T | 0.000101428 | 0.00712067 | missense | TNRC6C | GRCh38.p7 | 17:78091506 | TGTCGGTGAAGGACC[C/T]ATCCCAGTCCCAGTC | 57690 |
rs375547025 | snp | A/G | 3.54076e-05 | 0.00420744 | missense | TNRC6C | GRCh38.p7 | 17:78049138 | AATGGCACCAATGGC[A/G]CACTCGTCCAAAGCC | 57690 |
rs375547861 | snp | A/G | 6.67456e-05 | 0.00577654 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087107 | CGGTGAGTGTCCCAT[A/G]GTCTTCAACAGCCAC | 57690 |
rs375550999 | snp | C/T | 0.000396719 | 0.0140784 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064867 | CGGGTGGGGAGATCA[C/T]CCTGCAGAGCCGCCG | 57690 |
rs375567132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090535 | ACAAGGGGAGGGGGG[C/T]GCTTGTGCTGGTTAT | 57690 |
rs375585355 | snp | G/T | 1.80422e-05 | 0.00300346 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091390 | AGGAGAGCTTTAGAA[G/T]GAAGTCATTTAGAGG | 57690 |
rs375648922 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074968 | ATCCTTGGCAGCCCC[C/T]TGTTGGGCTCAGCCC | 57690 |
rs375650702 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015183 | TTCATTGTGTGGGGT[A/G]TCCATGCATAAGAGA | 57690 |
rs375657876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037107 | TGCAAGCTTGCTTCT[A/G]TAGAAAATTGCAACC | 57690 |
rs375666373 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073763 | ATGTTTTTCTGTTTC[A/G]AGACACCTTATTTAA | 57690 |
rs375678865 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107079 | TTCGATGGACATACA[C/T]CTGCGTATGTATATC | 57690 |
rs375719377 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102652 | TAGTTGGGGGTTCTT[C/G]GTCAGGGTCCATAAG | 57690 |
rs375746355 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023799 | CAACGGAAGTGAGAC[C/T]CTGTCTCAAAAAACA | 57690 |
rs375757134 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055869 | TTCCAAGGGTACATA[-/A]TGTGGGAGGGAGATG | 57690 |
rs375770372 | snp | C/G | 8.38624e-05 | 0.00647489 | missense | TNRC6C | GRCh38.p7 | 17:78086509 | TGTCAACAGGCATAC[C/G]AACGTTTACAAATCC | 57690 |
rs375777125 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089410 | TATTAAAAGCAAATA[A/G]CTAATAAAGTCTAGG | 57690 |
rs375793934 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008817 | ACTCGAAATTCCTCT[A/G]TCCTGAGATATTTAC | 57690 |
rs375803213 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010031 | TGACTACAGGTGCAT[A/G]CCACAGTGCCTGGCT | 57690 |
rs375824265 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076239 | AAAGAAAAAGAAAAA[A/G]AAAAAAGGAAAGGCT | 57690 |
rs375868701 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071314 | TAACTCTTAAATCTC[C/T]CTTTTACCTGGGTAG | 57690 |
rs375878349 | snp | A/C | | | missense | TNRC6C | GRCh38.p7 | 17:78086999 | CAAATCGGCCATGGA[A/C]AGCTTCCCCTCGCAC | 57690 |
rs375883260 | snp | A/G | 0.00013403 | 0.00818518 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077220 | GCCCACGCCTTCACC[A/G]TTCTTGCCTTCCCCA | 57690 |
rs375920778 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008944 | CACTCCTGGATCCCT[A/G]TCCCTTCAAGGAGCT | 57690 |
rs375933179 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095007 | AGACCCAGCCCTCCC[C/T]GCTTGTCACACCTGG | 57690 |
rs375953408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084258 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 57690 |
rs375959564 | snp | A/G | 1.68923e-05 | 0.00290618 | missense | TNRC6C | GRCh38.p7 | 17:78067768 | CTAGCTTCAAAATCT[A/G]TGCAAGAAGGCTGGG | 57690 |
rs375965650 | snp | C/T | 1.72119e-05 | 0.00293354 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050073 | CCGAAGCACCTCTAA[C/T]GGTGTGAATGGGGAA | 57690 |
rs375976879 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019304 | GTATCTTAGAGATGA[C/T]AATGTAGTAGAAAAG | 57690 |
rs375979784 | snp | C/T | 0.00024906 | 0.0111565 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093003 | CTCCTATGGCCGGTA[C/T]GATTTAATCCAGAAC | 57690 |
rs376002740 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039845 | GCTGTCCTGAGAGCC[C/T]GCTGCCCCCAGGCAG | 57690 |
rs376007413 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092101 | GGACACACGAGTAAG[G/T]TGGAAGCAAAAATGA | 57690 |
rs376025215 | snp | C/T | 1.65765e-05 | 0.00287888 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064771 | CTCAAAGACTGAAAA[C/T]TCTTGGGGAGAACCA | 57690 |
rs376048673 | snp | C/T | 9.96529e-05 | 0.00705808 | missense | TNRC6C | GRCh38.p7 | 17:78086953 | CACCGCCACCGCCCC[C/T]GCCGCACCTGTCTCT | 57690 |
rs376099669 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048021 | TTATTCTAGGGATCT[C/T]CAAAGAAAAGGCTCT | 57690 |
rs376104550 | snp | A/G | 8.52988e-05 | 0.00653009 | missense | TNRC6C | GRCh38.p7 | 17:78051095 | ACAACAATGTGAGTA[A/G]CTGGGGAGGAGCTGC | 57690 |
rs376109260 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100176 | GTGCAAGCTGTCAGT[A/G]GATCTACCATTCTGG | 57690 |
rs376113247 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069337 | AGTGCAGTTCCAGAC[A/G]GCACTCAGAGACACC | 57690 |
rs376115182 | snp | A/G | 0.0020752 | 0.0321448 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071175 | TTCCCGGTAACTGGC[A/G]TCGTAGTTTACTGCT | 57690 |
rs376131938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016852 | TCCTCAAGGAACTCT[A/C]TCAGTAAGGGATTCT | 57690 |
rs376154392 | snp | A/G | 7.25821e-05 | 0.00602377 | missense | TNRC6C | GRCh38.p7 | 17:78051221 | CACCGTCCATTCGCC[A/G]CAAAATGGAAATTGA | 57690 |
rs376157311 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054147 | ATATATCTAAACATG[-/A]AAAGGGGACATTAAA | 57690 |
rs376157920 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083798 | CTTGAAAGTTTTGTA[A/G]CTTCACATAATCTTG | 57690 |
rs376182712 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025034 | CCTGACAGGTGATCC[A/C]CCCACCGCAGCCTCC | 57690 |
rs376189252 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103262 | ACAGAGATATAAAAC[A/G]TTAATGTTGTAAAAC | 57690 |
rs376191745 | snp | A/G | 1.84055e-05 | 0.00303355 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064888 | AGAGCCGCCGGTGGC[A/G]TTTGGAAGAGCTGGC | 57690 |
rs376250597 | snp | C/T | 1.88677e-05 | 0.0030714 | missense | TNRC6C | GRCh38.p7 | 17:78091554 | CGCACCCCAACTCCA[C/T]GGATAACTTGCCCAG | 57690 |
rs376257263 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044823 | TTGTTTGCCACCCTG[G/T]TTGGTCTAAGTGACT | 57690 |
rs376329243 | snp | C/G | 1.66696e-05 | 0.00288696 | missense | TNRC6C | GRCh38.p7 | 17:78050984 | CTGGGAACAGTGGCT[C/G]GGGCAACAGCACAAA | 57690 |
rs376331483 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015804 | GTGATCCCAGCTACT[C/T]GGGAGGCCAAGGCAG | 57690 |
rs376341075 | snp | C/T | 6.73435e-05 | 0.00580234 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049266 | TCACTGCTCTGTCAG[C/T]GGTGGGGATGGAAAA | 57690 |
rs376342054 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036182 | CAGCTTCGCACACGA[A/T]TTTCTGTGTTTTTCC | 57690 |
rs376405094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061286 | CTATAAATTATTAAC[A/G]AAAAGATGCCAAATT | 57690 |
rs376413228 | snp | C/T | 0.000155988 | 0.00883004 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079427 | GGGTATGTTTGGCAA[C/T]AGTGGAGCAGCACAA | 57690 |
rs376429470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092659 | CCAAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 57690 |
rs376467730 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006551 | CTTCTTCTTCTTCTT[-/C]CTTCTTCTTCCTTCT | 57690 |
rs376507159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088137 | GTCTCTGAAAAGAGC[A/G]GTATATTGTAATCAT | 57690 |
rs376514875 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103785 | CCTTCTCCCTCTGTT[C/G]TTATATGGTCGTCTC | 57690 |
rs376603128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014188 | GATTTAGGATTTGCC[A/G]TTTGTTCTGAGAGCT | 57690 |
rs376624363 | snp | A/T | 0.000165986 | 0.00910854 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071067 | ATGGACTTCCCCCTT[A/T]CCCACACTTTGTTCA | 57690 |
rs376642000 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105130 | TTTTTTTTTTTTTTT[A/G]AGTATAAAAGCTGCT | 57690 |
rs376659597 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005316 | TTAGCTTTCCAAACA[A/G]TGCTTTTAAATTTTC | 57690 |
rs376712486 | snp | G/T | 9.9369e-05 | 0.00704802 | missense | TNRC6C | GRCh38.p7 | 17:78079504 | ACTCTTCCCAGCCCA[G/T]TCTCCGTGCTCAAGT | 57690 |
rs376714178 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051627 | AGTGAGAGCAAAGTA[A/G]GATCCTCTGGTGGTT | 57690 |
rs376718734 | snp | A/T | 0.000163987 | 0.00905352 | missense | TNRC6C | GRCh38.p7 | 17:78050356 | ATAGACCAAGGGCAC[A/T]TCCAGTTGCCAAGGA | 57690 |
rs376724539 | snp | C/T | 0.000340851 | 0.0130503 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102436 | CACTATCCACTGGCA[C/T]GGGGCCTTGTCAACC | 57690 |
rs376745906 | snp | A/G | 3.62083e-05 | 0.00425474 | missense | TNRC6C | GRCh38.p7 | 17:78050161 | GGGTGGGAGAGTCCT[A/G]GTGTCACCAGCCAGA | 57690 |
rs376785391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028596 | TGTGGACAATGTAGC[A/G]TTCACATGGTAGATG | 57690 |
rs376787878 | snp | C/T | 1.65767e-05 | 0.00287891 | missense | TNRC6C | GRCh38.p7 | 17:78103504 | GGCAATGCTGTGGTC[C/T]GGTACAGCTCCAAGG | 57690 |
rs376803332 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044018 | AGTAGTGCTGCAGCA[A/G]ACATCGAAGCTCTCT | 57690 |
rs376822136 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065136 | GGAGGATCGCTTGAG[C/T]GCAGGAGTTTGAGAC | 57690 |
rs376848476 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105570 | TCAGTACACAGAAAC[A/G]GGCTCTAGGAAAAAT | 57690 |
rs376860207 | snp | A/G | 1.66272e-05 | 0.00288328 | missense | TNRC6C | GRCh38.p7 | 17:78086925 | GCCCAGGCCCTGCTC[A/G]TGAAGCAGCCACCAC | 57690 |
rs376879001 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034952 | CCAGCCTGGGCAACA[A/G]GAAAAAATAAATAAC | 57690 |
rs376885702 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054888 | TGCAGACTACTGTAC[A/G]CTACCATACACCACT | 57690 |
rs376891403 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027369 | TGATGAGAAGGAGCT[A/G]ATTACAGTAGCCAGA | 57690 |
rs376893670 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005116 | GGGTACATTTATGGC[-/G]GGTACCAAAATTTTT | 57690 |
rs376901842 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052709 | CCCTACAGGACCTCC[A/C]CTGGCCCACCAGCTG | 57690 |
rs376934853 | snp | A/G | 3.35644e-05 | 0.00409647 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086589 | ACAGGAGCAGCAAGT[A/G]GGTGCTACCCAGATT | 57690 |
rs376938262 | snp | C/T | 1.82012e-05 | 0.00301666 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050715 | TAGTACTGCTGCTGC[C/T]GCCAAGAGTGGCCAT | 57690 |
rs377028000 | snp | G/T | 0.000179984 | 0.0094847 | missense | TNRC6C | GRCh38.p7 | 17:78051327 | GGTCATCCAGAGCAG[G/T]ACCACGACCAATACC | 57690 |
rs377100844 | snp | A/G | 0.000140647 | 0.00838473 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067712 | GGAAGCATTGTCTGC[A/G]TTAGGGACATGAATT | 57690 |
rs377129562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043290 | CCACAGTGTGGCCCC[A/G]AGGCTGCAGCCTATC | 57690 |
rs377135018 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080174 | AAATGTTGCCGGGCG[C/T]GGCGGCTCACGCCTG | 57690 |
rs377148817 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104897 | CCCGGGACCCCTCCC[A/G]GCTGGGCGGCCCCAC | 57690 |
rs377238735 | snp | A/G | 0.000163987 | 0.00905354 | missense | TNRC6C | GRCh38.p7 | 17:78049778 | CTCAAGTCAGTGGGG[A/G]CAGTGCTGAAGGAAT | 57690 |
rs377253780 | in-del | -/TTACCCACCATGC | 0.000597788 | 0.0172782 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071181 | TAACTGGCGTCGTAG[-/TTACCCACCATGC]TTTACTGCTACCCAC | 57690 |
rs377307256 | snp | A/T | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031523 | CATTTTAGTGCCAGA[A/T]CCTACTAAGACCTGT | 57690 |
rs377315255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098843 | TCAGGAGTGTGGCTG[C/T]CCCACACTGGGCCAT | 57690 |
rs377331679 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094884 | GATGCAGCTGCGTTT[C/T]GGAACAGGGATGTTA | 57690 |
rs377372426 | snp | A/G | 1.66021e-05 | 0.0028811 | missense | TNRC6C | GRCh38.p7 | 17:78049868 | GGTTCAGTCAGGGGA[A/G]TGGAGACACTGTGAA | 57690 |
rs377405828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016368 | CTGGGGGAACCAGAT[A/C]CCTAGCCTCAGCTCT | 57690 |
rs377419618 | snp | A/G | 3.23651e-05 | 0.00402262 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78071150 | GATCAAACAACTCAC[A/G]GACATGGGCTTCCCG | 57690 |
rs377427587 | snp | A/G | 0.000190458 | 0.00975668 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78097848 | CAGCATTGCATCCGC[A/G]CCTAGTGTTGCAGGT | 57690 |
rs377456456 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047519 | TTAGGTTGATATTAG[C/T]TTTAGTATGGTCTTT | 57690 |
rs377571209 | snp | C/G | 4.97756e-05 | 0.00498852 | missense | TNRC6C | GRCh38.p7 | 17:78050465 | AAGAATCCCCTAGGT[C/G]TGAAAGGAAAAATGA | 57690 |
rs377573376 | snp | A/G | 0.000323948 | 0.0127228 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102571 | TGCCCCTGCATCACT[A/G]AGCATGATCCAGGGA | 57690 |
rs377635136 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021021 | TCCAGTGCCTTCCTA[C/T]GGCAACCAACACAGT | 57690 |
rs377643255 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080376 | GCTTGACCCGGGGAG[A/G]TGGAGATTGCGGTGA | 57690 |
rs377678893 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025227 | AATCCCCTGTGCTCC[A/G]CATAGTCATCCCCCA | 57690 |
rs377689264 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108719 | GTCCAGGGCACCATT[C/T]CCACCCATGGGTGAA | 57690 |
rs377691595 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074584 | TTAAGCCAACAGAGC[C/T]GTGAGAACAGAAACA | 57690 |
rs377695517 | snp | A/G | 5.11801e-05 | 0.0050584 | missense | TNRC6C | GRCh38.p7 | 17:78098384 | TGGTCCTCTGGCCCT[A/G]CCTCCCACACGCAAG | 57690 |
rs377699640 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083348 | GTGTCCTACTAGGTT[C/T]TGTAAATGTTTTGGC | 57690 |
rs377730363 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025257 | ACTCCCCTGGCAACC[A/G]CTGATCTTTTCACCA | 57690 |
rs377749176 | snp | C/T | 8.51535e-05 | 0.00652453 | missense | TNRC6C | GRCh38.p7 | 17:78067760 | CTCTGTTTCTAGCTT[C/T]AAAATCTATGCAAGA | 57690 |
rs377751957 | snp | C/T | 1.66092e-05 | 0.00288172 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78092994 | CATTGATGACTCCTA[C/T]GGCCGGTACGATTTA | 57690 |
rs377765102 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047087 | TGTCTTAGTCAAGAG[A/G]CAGCCTGCCTTATGG | 57690 |
rs386799485 | multinucleotide-polymorphism | CG/TA | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012575 | AAGCAAATATATGTA[CG/TA]TGCAAATGAATGCAA | 57690 |
rs386799486 | multinucleotide-polymorphism | AGA/GGG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063701 | TGTGGGTGGTACCAT[AGA/GGG]AACTGTCTGCATTTT | 57690 |
rs386799487 | in-del | C/TG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084303 | AAAAAAAGAAAATCA[C/TG]ACCAGGAATCATGAA | 57690 |
rs386799488 | multinucleotide-polymorphism | AGC/GGT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101558 | ACACAGAAATAGAGC[AGC/GGT]GTGAAGTGGGAAATC | 57690 |
rs397686424 | in-del | -/A | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062353 | ATTTTCTTAGAATAA[-/A]GAGTATCAAGGGAAC | 57690 |
rs397808772 | in-del | -/TG | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105649 | GTGTGTGTGTGTGTG[-/TG]CATGTGTGGCGCGTG | 57690 |
rs397809464 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030343 | TGTGTGTGTGTGTGT[-/GT]AGTAGAGACAGGGTT | 57690 |
rs397951200 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091341 | AAAAAAAAAAAAAAA[-/A]TTTGCTGTAAGCGAA | 57690 |
rs397965010 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066243 | AAAAAAAAAAAAAAA[-/A]TTCGTTGTTCACATA | 57690 |
rs398031689 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039321 | TAAGAGGTAGGGAGT[-/G]GGGGGGGGGGGCAAG | 57690 |
rs398100640 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077099 | ATTTATCCATCCACG[-/G]CCTCCTCTGTTTCCT | 57690 |
rs398120042 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069219 | GATTTAAAAAAAAAA[-/A]TCAGCCAGAAACCCA | 57690 |
rs527241519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070614 | AGTAACAAATAGTTA[A/G]TAAAATTAACAGGTT | 57690 |
rs527244972 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016098 | TGGGCCTTCAGAAAT[G/T]ACTCCCCAAAGAGTT | 57690 |
rs527246720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076779 | CCCTATGAAACTGCT[C/G]TGTTTGTAGGTCAAA | 57690 |
rs527254930 | snp | C/T | 0.000188342 | 0.00970234 | missense | TNRC6C | GRCh38.p7 | 17:78051365 | CCACCACCACTACCA[C/T]GAGCAACACCACACA | 57690 |
rs527293195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083428 | GCTGGTCTGGAACTC[C/G]TGGACTCAAGGGATC | 57690 |
rs527305582 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067412 | TAGGAATCTACATTT[C/T]TGTAGCCTTTTCATA | 57690 |
rs527328011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076314 | AGTCCTCCAGCACGT[G/T]ATCTGCCTCAGCTGC | 57690 |
rs527334113 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098715 | GTAGCTGGGTGAGCC[C/T]GGTGTTTTTAGCATC | 57690 |
rs527335208 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048399 | TGAAAGCCATGTTTC[A/G]CCTCTATATAATACT | 57690 |
rs527356303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036917 | TGACAGAGCAAGATT[C/G]CATTAAAAAAAAAAA | 57690 |
rs527439220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057118 | TTTTTCCATGTGGAA[A/G]TGTGCTCACATGCTG | 57690 |
rs527453002 | snp | A/G | 8.49317e-05 | 0.00651603 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064946 | AAACCAGGTAAGCCT[A/G]GCATCCTGCTTGCCC | 57690 |
rs527505977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103088 | CCAAGTCTGTTGTCA[A/G]CAGCTGGACCCAGGT | 57690 |
rs527525681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064097 | CGCCCAGGCTAGAGT[A/G]CAGTGGCACAATCTT | 57690 |
rs527564989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070976 | AATGTTAATACAAAA[A/C]GATCCTGTGACTTTT | 57690 |
rs527624298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030705 | TAAATTCATGGACAC[C/G]TAAAGATTCCTTCGT | 57690 |
rs527628336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024647 | TGGGATTACAGGCGT[C/G]AGCCACCGCGCCTGG | 57690 |
rs527723950 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011554 | TTCCATTGTGTAGGT[A/G]TATCACAGCTATTTA | 57690 |
rs527762511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011993 | ATTGTTATTTATTTT[C/T]TTTTTCCAGATTGGT | 57690 |
rs527784507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097285 | GGGACACCCCAGTCA[A/G]AAGAAATACTCAAAT | 57690 |
rs527788325 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009245 | TGAGTAATCAGTTTT[C/G]TTTATTTTTGGCACT | 57690 |
rs527801594 | snp | A/G | 1.67002e-05 | 0.00288961 | missense | TNRC6C | GRCh38.p7 | 17:78050987 | GGAACAGTGGCTGGG[A/G]CAACAGCACAAATAC | 57690 |
rs527802080 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057825 | TTCTGAATTACATTT[G/T]TGTGTGTGTGTGTGT | 57690 |
rs527813793 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018457 | TTTATATAATACTCA[A/C/G]TATTCACAGTGCCTG | 57690 |
rs527823747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096607 | CAACGCCATGTGGGC[C/T]TACGGCTGAGATGCC | 57690 |
rs527827137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011570 | TATCACAGCTATTTA[C/T]CCTCTTCATTCTCCT | 57690 |
rs527830451 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072853 | GAAAATCAAGTCAGT[A/G]CATTTTCTTATTACA | 57690 |
rs527855216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100361 | CATCCAGGCATTTCC[A/G]TATATCCTCTGAAAT | 57690 |
rs527878352 | in-del | -/AGATA | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044206 | CTAACTTCTCTGAAT[-/AGATA]ACCCAGTATTTTTGC | 57690 |
rs527925880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078965 | GGGTATGGTGGCAGG[C/T]GACGGTAATCCCAGC | 57690 |
rs527926110 | snp | A/T | 4.96192e-05 | 0.00498067 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098293 | AACACAGCAGTGAGT[A/T]TTCTTCTTTGTCTCA | 57690 |
rs527952043 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038536 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 57690 |
rs527959339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031454 | TGGTTTCCTTGGTTT[C/G]GGTTGGGTTTTAAAG | 57690 |
rs528067063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059569 | AATACAGTGTGAGGC[C/T]GGACACAGTGGCTCA | 57690 |
rs528095000 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105375 | TGCGATCTGCTCTCT[C/G]TTCCCCTGGATCCGC | 57690 |
rs528100975 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037689 | TGTAAGGCTACAGAA[A/G]TTGGCTGTTGGTATT | 57690 |
rs528106431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066546 | CACAGTTATGTGCCT[A/G]TTCCATATGTTTATC | 57690 |
rs528110361 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073872 | ACTCAAAACAATGCC[A/G]TCCACCACACTTCCT | 57690 |
rs528147137 | snp | C/T | 0.00103896 | 0.0227684 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104761 | GTGGGGCCCGCCCAG[C/T]GCCGACGACAGCAGG | 57690 |
rs528155047 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027165 | GGTCCAAAGACTGAG[C/G]GGTCAAAAGATAACA | 57690 |
rs528155071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019452 | TATTTGGCCCTGTTA[C/T]GACAACACTACCTGA | 57690 |
rs528162533 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040832 | AAATCCCATCCGTCC[A/G]TGCCTCCGCCCCTAG | 57690 |
rs528191278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066031 | AGGTCAGGAGTTCGA[A/G]ACCAGCCTGGCCAAC | 57690 |
rs528193374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073337 | TTCTCATATTTTCCC[A/G]TTATGTTTTGAGGGA | 57690 |
rs528242696 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088643 | CTCTCTTTTTTTTTT[C/T]GGCTGGAGTGCAGTG | 57690 |
rs528243060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026670 | ACCACGTGGACCTTG[C/T]AGAGAGTTTGGATTT | 57690 |
rs528274172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039315 | TCAAATCTTGCCCCC[C/G]CCCCCCACTCCCTAC | 57690 |
rs528285389 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102364 | GGCTTTCCTAAAGCA[C/T]GCAGTGACGGCCTGT | 57690 |
rs528300488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085966 | ATTGACTCTGTGATT[C/T]TTTTTAGTTCTGCGC | 57690 |
rs528306308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007001 | CACGCATGGCCACAC[A/C]CAGCTAATTTTTTGT | 57690 |
rs528315490 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087310 | TTTTGAGAGATGGGG[G/T]TCTCACCATGTTGCT | 57690 |
rs528320905 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053497 | AGCCGGGCATGGTGG[C/T]GCATGTCTCTAATCC | 57690 |
rs528328688 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018465 | ATACTCAGTATTCAC[A/G]GTGCCTGGCACAGAA | 57690 |
rs528360226 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023331 | CAGTGTCAGTTATTT[-/A]ACAAAAGAGAAACTG | 57690 |
rs528363389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092207 | AATTCAGTAGGTTAC[C/G]TAGTTCTCTCTTGAT | 57690 |
rs528369337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099615 | GTTAACCTCCCACTG[G/T]GTTCCTTCACGAAAC | 57690 |
rs528381000 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053093 | TACCATGTCACGTTG[C/T]CCCCCGACCCCTGAC | 57690 |
rs528402059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098908 | CCATGACTCCCCTTC[A/G]CACAGGGATCTGGAT | 57690 |
rs528415064 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013671 | TGTGTGACAGCATCA[A/G]CAAAGGAGCCCAAAC | 57690 |
rs528452898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067459 | ACCTTCCCTGGTGGC[C/T]CCAGGATTTGTTCTT | 57690 |
rs528454451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074481 | TGGTGCAAACTGCCA[A/G]GGCGGGACAGAGCAG | 57690 |
rs528461335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028022 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTGCA | 57690 |
rs528517400 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106917 | TCCTGCAAGACTGCA[C/G]ATCCACAAAAGCTGG | 57690 |
rs528530894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081018 | GTCATTTACAACAGC[A/G]TGAATGTATTGCTTG | 57690 |
rs528541346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074018 | GGATGTACCATATCA[C/T]TGATTCATGATCATT | 57690 |
rs528550299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033962 | GGTCACCTAGTTACT[A/C]ATGCACAAACTCTCC | 57690 |
rs528669698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054347 | ACTGCACACTACTGC[A/G]GACTACGCACACCAC | 57690 |
rs528700435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100608 | CATTTTTTCCTTGTA[A/G]GCCTCTGGGCCTGTG | 57690 |
rs528721662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022046 | CTTTGGGCCAAAAAG[A/G]TGCCCAGAGGCAGTG | 57690 |
rs528737056 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107514 | ATGTCTACTTTGCAC[A/G]CTGCGATTGGGAGAG | 57690 |
rs528795593 | snp | A/G | 6.68986e-05 | 0.00578315 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083206 | TAGAGCACGCAGGCC[A/G]AGTGCAGATGCACGG | 57690 |
rs528807434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021558 | AGGAGACATGGAATA[G/T]GTTATTTATTTTTTT | 57690 |
rs528834487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069146 | CAAACTGGAAAAATA[G/T]GTTTATAACTCATAT | 57690 |
rs528837896 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041355 | TGGCTTTCCCTACTG[A/T]GGTTTCTCTCTGCTG | 57690 |
rs528921714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048497 | ATTGCCAGTGTTTCT[C/G]AGTCTCTGTATTTAT | 57690 |
rs528959205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009032 | ATTCTGCTGAATATC[A/G]TCTTTGCGTTGGTGA | 57690 |
rs528962384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047634 | TTTTAATTGTCCATA[A/C]GATTTTTCTTGTTAA | 57690 |
rs528990216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015452 | TTAAAATATACTGCT[C/G]TCATCCATTTCACAC | 57690 |
rs528993668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094308 | ACAGCATGCTATTTT[A/G]TGGAAGGAAGAGCTA | 57690 |
rs529009825 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023023 | GGGCATGGTGGTATG[C/T]ACCTATTGTCCCAGC | 57690 |
rs529017419 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008049 | TCCTGGAGAATATTA[A/T]CTAGTCTAATCCGTT | 57690 |
rs529085318 | snp | C/G | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012006 | TTCTTTTTCCAGATT[C/G]GTTTCTGATACTAAA | 57690 |
rs529091951 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039431 | CATTGGTTTTGTAGC[A/G]TTATTGATGTCAACA | 57690 |
rs529128696 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029021 | TATTAGGTTATCACC[C/G]AACTCTTCTGCTCCT | 57690 |
rs529148760 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044099 | AGTATAACTTATTAT[C/G]AAACCCTATCTATGT | 57690 |
rs529212688 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040927 | CGGCCGCGGGCGCCC[A/G]CGGGTGGCCCGGACG | 57690 |
rs529236085 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036689 | AGCAGTTTGAGAGGC[C/T]GAGGCAGGTGGATCA | 57690 |
rs529240110 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056784 | AACTACTTTTAACTT[A/G]TTTTTAGTAGCCAAA | 57690 |
rs529272664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010173 | AGCCACCAGCTCAGC[C/T]CAAATTCGTACATTT | 57690 |
rs529280802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055990 | TGCATTTGTTGGGGG[A/T]TCTCTCCCCTTTGAT | 57690 |
rs529329635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016782 | TATAAACGCTTACTG[C/T]GTACTAAGTGCCAGT | 57690 |
rs529334570 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022325 | GGCAGGTAGCACACA[A/G]GAAACCATATTCCAT | 57690 |
rs529368009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070444 | ACCTTTGCATTTATA[A/G]GCTCAGAGGGAAGTT | 57690 |
rs529403153 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062843 | GGACTTCCCAAAAAC[C/T]TAACTACTTGACCAG | 57690 |
rs529409930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108873 | TTGTTAATACAGGGT[C/T]TCTGTCTCCCACGCT | 57690 |
rs529415278 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030188 | GGAGTCTCGCTCTGT[A/C]ACCCAGCCTGGAGTG | 57690 |
rs529433755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023943 | GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA | 57690 |
rs529455894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090031 | TACCTGGCTAGATCT[C/G]TACAAGCTGAAACGA | 57690 |
rs529462367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083540 | ATCTACCAATCTACC[A/G]GATTTTATAATTAGG | 57690 |
rs529474446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082911 | GGAGCATTTCATCTT[C/T]TATTCCATAGCAGTA | 57690 |
rs529491393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043669 | TAATTACTAGGTCTT[A/T]TTTATTCTTTCTGAT | 57690 |
rs529495340 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090109 | GATGGGCTTGCAAAG[A/G]CGTTTTGTTAGGTCT | 57690 |
rs529537922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011436 | GTATTGAGGGACTCC[C/T]ACACTGTGCACTTTG | 57690 |
rs529567338 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005720 | CTCAGGAGTCACATA[A/T]ACTAGCTCTGTTTAA | 57690 |
rs529571155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103858 | AGTCCTGTTGGACTA[A/G]GGCCTACCCATGTGA | 57690 |
rs529577341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095910 | GAAAAAATTAGCTGC[A/G]TGTGGTGGCACACGT | 57690 |
rs529580575 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068542 | CTCACACCTGTAATC[C/G]CGGCACTTTGGGAGG | 57690 |
rs529620104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071915 | AATTCATAATTGTAG[A/G]GCGTTCCCCTGAAAA | 57690 |
rs529687503 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018689 | TATTGATCCTTTTTC[C/T]CTACTAAGATGTGAG | 57690 |
rs529703538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078045 | CTTGGAGACATGTCT[C/G]TAAGTAGACACTGTG | 57690 |
rs529710034 | in-del | -/T | 0.411623 | 0.19073 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042568 | GTCATTTCACAGATT[-/T]TTTTTTTTTTTTTAA | 57690 |
rs529728596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084114 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 57690 |
rs529744606 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030816 | TAGAAATGCAAATTC[C/T]GGCCGGGCATGGTGG | 57690 |
rs529762478 | snp | A/G | 0.000157872 | 0.00888319 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071178 | CCGGTAACTGGCGTC[A/G]TAGTTTACTGCTACC | 57690 |
rs529806325 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107519 | TACTTTGCACGCTGC[A/G]ATTGGGAGAGCTGTC | 57690 |
rs529853454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037531 | GGTGATATGAGCTGA[A/G]TTTCAAGTTAGCTGT | 57690 |
rs529904511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058615 | TTACTGTGTCTTCCA[A/G]CAATGGCTAGAAGTA | 57690 |
rs529915958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097376 | GTTTGAACTGTGAAA[A/G]GATGTAGATTGCCCT | 57690 |
rs530012163 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038596 | AGGCAGGAGAATGCC[A/G]TGAACCCGGGAGGCG | 57690 |
rs530088750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085787 | ACCAGTGTTTCACAT[A/T]GTCTGGGCTGTCCTG | 57690 |
rs530102201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044956 | GACATTGAGCCCAGG[C/T]AGGGGATGGCACCTT | 57690 |
rs530120318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084754 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 57690 |
rs530126586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091976 | AATATACAGTATGTA[C/T]GGGAACTGCAGCTGT | 57690 |
rs530138090 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052234 | TGGAGGAGGGCTGGC[G/T]AGGAGCAGCAGCACG | 57690 |
rs530164706 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097947 | CAGCTTTTCCTATTG[G/T]CTCTTTACTCACTCC | 57690 |
rs530245693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091011 | ATTTTCCTGTGGACT[C/T]TGAGAAGCCTCAGGA | 57690 |
rs530246269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027375 | GAAGGAGCTAATTAC[A/G]GTAGCCAGACAGTCC | 57690 |
rs530276054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073809 | CAAGAAGGGTGTAAC[A/G]TTTTTCTGACCCTGG | 57690 |
rs530278995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073423 | ACTGAGTGCGTTCCT[C/T]GTGCCTTGCCCCAGA | 57690 |
rs530281564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033323 | ATTAAATATTTATCT[C/T]TGTAAATATAACATT | 57690 |
rs530361679 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075338 | GAGTTTTTCATTTCA[A/T]CTGTGTCCTTAATAC | 57690 |
rs530363501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039124 | GGAACGTGTCGAGAG[A/G]CAGTAGGGACAAAAA | 57690 |
rs530396051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100522 | CAGTCACAACTGGAG[C/T]GGCTGGGACACAAGG | 57690 |
rs530442368 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099721 | ACCCCTCCCAAATCT[A/C]ATGTCCTCACATTTC | 57690 |
rs530449759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060110 | AAACAGAGTCCCCTG[A/G]CTTTGGAATGGAAGT | 57690 |
rs530463744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032201 | TCCTAGTCTGTCTTA[G/T]GAGTGCACACAAGCA | 57690 |
rs530479429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007097 | ATTCCCCCCCACCTC[A/G]GCCTGCCAAAGTGCT | 57690 |
rs530533970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059602 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGC | 57690 |
rs530574689 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106238 | CTTTAAAATTTTAAA[A/G]ATTTAAAAAGGAATT | 57690 |
rs530588040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034097 | TCTCTCTTGTTGCCC[A/G]GGCTGAAATGCGATG | 57690 |
rs530598046 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107152 | GACATACCACTTCCC[A/G]TGCTGCCGGCGAGCA | 57690 |
rs530607839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013711 | GTTGTGGAAGGTATC[A/G]TTGAATCTGAAGGGT | 57690 |
rs530664382 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105477 | TAAAAAAAGACATAT[C/T]AAACATGCAAATACT | 57690 |
rs530700931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040649 | CCTGCAGCCAATAGG[C/T]AAAATGCCGTTATTC | 57690 |
rs530714989 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046397 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 57690 |
rs530743156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092822 | ATGTAACTGAATAGG[A/G]CAAGGCATTGGACCT | 57690 |
rs530768016 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057486 | TGGCAGCCCCTTGCC[C/G]TCCTCTCTGGGGACT | 57690 |
rs530771434 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091667 | ATTAATCGATCGTCC[G/T]GTTGTATAGCATGGC | 57690 |
rs530789849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039827 | CATTTCAGCTGTCAA[A/G]GGGCTGTCCTGAGAG | 57690 |
rs530825533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007730 | GATACTCTTAAGAGA[G/T]AAGCTGCAGTTATAA | 57690 |
rs530848127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068015 | AGACAAAAAGATAGA[C/T]CTGAGGTTCTCAAAG | 57690 |
rs530852396 | in-del | -/AG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083583 | GTTGAGCTCTCAGCC[-/AG]AGTTTCTGAGAACCA | 57690 |
rs530889135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081588 | CTCTCAGGTTACAGT[A/G]CAGAAAGAAGCAGTG | 57690 |
rs530951831 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082952 | GTCTCCCTACAAATT[A/G]TCATTTAATCATTTT | 57690 |
rs530952093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028922 | TGACTATTGAGGCGC[C/T]GACTCTTGCACTTTA | 57690 |
rs530981176 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051663 | TTCAAGAAAAAAATA[C/T]ATTAAGCACACTCAG | 57690 |
rs531015112 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081738 | CCTAGGCCACAGCTG[C/T]ACCCAGTCTGAGAGG | 57690 |
rs531030553 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094412 | TGACTCATTGGAGCC[A/C]TGTGTTTTGTGTTTG | 57690 |
rs531067246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101418 | TTTCCCACATTCTCC[C/T]GTCTATTTCTGAGCC | 57690 |
rs531070857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034651 | AGAGTCTTGCCTTTA[A/C]ACTAAGTTGGAAATA | 57690 |
rs531116341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055204 | TTTTTTATATTCTTA[C/T]TCTATGAGCTTTTTT | 57690 |
rs531149921 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108251 | CCCCGCCACAGGCTG[C/G]CCCCCCCCCACCCAT | 57690 |
rs531151974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101909 | GTCACAGTGCTGCAG[A/G]GAGTTTTTTTTATGG | 57690 |
rs531154610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062617 | TATCAACAGTGTCAG[A/G]TGAGCTTATGGCAGA | 57690 |
rs531174289 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030053 | CTCTAAAATAATGAT[A/C]AAAAGCATAGTAAAT | 57690 |
rs531184621 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042682 | GATGATGATGGTGCT[A/G]TTGGTGATGGTGATG | 57690 |
rs531208721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089487 | TCTGCAGCAGCACCT[A/G]TGTTGAAGAGCCTGT | 57690 |
rs531239061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028052 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 57690 |
rs531251236 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071608 | GGCCAGGCTGGTCTC[A/G]AACACCTGGGCTCAA | 57690 |
rs531264789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023040 | CCTATTGTCCCAGCT[A/G]TTTGGGAGGCTGAGG | 57690 |
rs531401071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041987 | CTGATACCTAATTAA[A/G]ATTTTGCTTACTATG | 57690 |
rs531465465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094976 | AGAGGACAGGTGAGG[C/T]GCCAGCCAGAATCAG | 57690 |
rs531527960 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006248 | CTAGAGTCACATGAA[A/G]AGAGGGAGTTAATGC | 57690 |
rs531528151 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046910 | ATCCTCAAGTCCTCA[A/G]AGTAGACCATTAACA | 57690 |
rs531609090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076292 | TGGGACTTGATCTTA[C/T]TTTGAGAGTCCTCCA | 57690 |
rs531631148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056801 | TTTTAGTAGCCAAAA[C/T]ATGGGAGCTTCATGC | 57690 |
rs531638863 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006375 | TCCAAAAGGTTTATG[A/G]TACATAGTTGTGTAT | 57690 |
rs531696751 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003730 | GGGGGAGAAAAGATA[A/C]ATCACCCTGAAATTT | 57690 |
rs531703929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017701 | ATAGGTCAAGTGATA[C/G]AATCCAAAATCCTTC | 57690 |
rs531740628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025051 | CCACCGCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 57690 |
rs531754761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078143 | CACTCACCAGCGCCC[A/G]ACTGTGTGATCCTGG | 57690 |
rs531759530 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011516 | TGTATCAGTAGTTCA[A/C/T]TCCTTTTTATTGCTG | 57690 |
rs531790829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102904 | GCACTTTGGGAGGCC[A/G]AGGCCAGGGATCACC | 57690 |
rs531822908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010935 | GTGAAACAAAGGAAG[A/T]GAGCCTAGCGGCAAG | 57690 |
rs531899343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090684 | CAGGTCCTGGACAAA[C/T]AACCAGGTACCTGCT | 57690 |
rs532015148 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037605 | GCATGCATGAAAAGC[A/G/T]CAGACCCGCAGTTGT | 57690 |
rs532039626 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004114 | AGCTAGTGCTTTTTC[A/G]TTGTTTGACTTAACA | 57690 |
rs532041385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043757 | CCCTTCCTAGCCTCT[A/G]TCTTCATAAGTTCAA | 57690 |
rs532050029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072478 | CTCACTGGGACAGGA[A/G]TCCTGTCCTAGGAGA | 57690 |
rs532054845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078920 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57690 |
rs532133931 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006242 | TCTAGACTAGAGTCA[A/C]ATGAAGAGAGGGAGT | 57690 |
rs532163426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026598 | GCTCACAGGGGAGTT[G/T]AGCACTTGCTGAACC | 57690 |
rs532175176 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026267 | GTCATTTTAAAAAAT[A/C]ACATACACAATGCTG | 57690 |
rs532187621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025850 | TGGACATAGGGAAGA[A/G]GAAATCCGTGGACTC | 57690 |
rs532227002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098029 | AGGCACAGTGGGCAC[A/G]CTGGGCACATCAGCT | 57690 |
rs532227018 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105210 | GGTTATTTTATCTGT[C/G]GGGGAGGGAGGGAGA | 57690 |
rs532333405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045053 | CAGGAGAAAGAATGA[C/T]ATGAATGGCCTCAAA | 57690 |
rs532350628 | snp | A/G | 2.94998e-05 | 0.00384045 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091610 | CCTAGCAAGCATGGT[A/G]CGTCTGAGCTAGGAT | 57690 |
rs532356736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013491 | TTTGATCCAGCAGAT[A/G]TTTATTGAGCACCTG | 57690 |
rs532385269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052402 | GTACTAGGCTGTACT[C/T]TAGTAGCTGGGGAAA | 57690 |
rs532470300 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058651 | TCATTACATATGCCA[A/G/T]TCAGAAAACTGGCAG | 57690 |
rs532517584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080225 | GCCGAGGTGGGTGGA[G/T]CACCTGAGGTCAGGA | 57690 |
rs532524939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092093 | TTACTGATGGACACA[A/C]GAGTAAGGTGGAAGC | 57690 |
rs532556227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079640 | ATTTTAAAGTGAGAG[C/T]GGAGTTAATCCATGT | 57690 |
rs532556509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060307 | GTTCCTCCATAAGCA[A/G]GTACCCAACCAGCCA | 57690 |
rs532714235 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033833 | CTCCCAAACAAAAAT[C/G]TTCATTTTATACCAA | 57690 |
rs532787071 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052413 | TACTCTAGTAGCTGG[A/G]GAAACTGCAGGAAGC | 57690 |
rs532800239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054321 | GCAGACTACGCACAC[C/T]ACTGCAGACTACTGC | 57690 |
rs532800864 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081098 | GTCTGGTGAGGGCCC[A/G]TTTCTCATAGATGGC | 57690 |
rs532810292 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004962 | TAAAATTTTCAATAC[C/T]AAAAGTTTGCTTATA | 57690 |
rs532837693 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078762 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCAGGAC | 57690 |
rs532883702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053770 | GATCTGAGAGCCCCC[A/G]CCTGTAATCCCAGCT | 57690 |
rs532931435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074948 | CCCCCATCCCCTTGC[C/T]GTGAATCCTTGGCAG | 57690 |
rs533019689 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78048915 | GCCTACTTACAGAAG[A/C/T]GAAGCCAACTGCAGC | 57690 |
rs533031731 | in-del | -/TC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024394 | TTTTTGGAGATGGAG[-/TC]TCTCTCTGTCTCCCA | 57690 |
rs533041178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014711 | AAAATACCTCTGAAC[A/G]GCATTTCTCATTAGC | 57690 |
rs533062234 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094173 | TTTTAGTAGAGACAG[A/G]GTTTTGCCATGTTGG | 57690 |
rs533069595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048458 | CTACAAGTTTTATTC[A/G]AAACTCTACGTGAAC | 57690 |
rs533070054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060812 | ATGTAAGTGGCATCT[A/G]TGGAACAAGCTATAA | 57690 |
rs533078298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021998 | AGTAGTTGGAACTCT[A/G]TTAGTATCTGGCTCT | 57690 |
rs533095943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099909 | ATGGGGGTACAGGCA[C/T]TGGGTAAATACAGTC | 57690 |
rs533098371 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107404 | ATCGAAAGTTGCTTT[C/T]GAAAGTACAACGCTT | 57690 |
rs533104766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087484 | GTTTTGCCGCTGCCA[A/G]TAATACTCTCAGTAT | 57690 |
rs533110248 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066362 | TTTTGGTTTTTTTTG[G/T]TTTTTGTTTTGCTAA | 57690 |
rs533115611 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062768 | ACCTCTTCTGTGCCT[A/G]TAGATAATGCAGTTG | 57690 |
rs533201289 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060365 | GGCCGTTGGTATGAG[G/T]AAAAAATCTCATCTC | 57690 |
rs533215324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061847 | TTTAAGAGGAATTTT[A/T]AATTCTTTATAAAAA | 57690 |
rs533230309 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108276 | ACCCATGGGGAAGGT[A/G]GTGTGCTGCTGGCTC | 57690 |
rs533247885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087891 | ACATACCTGAAGACA[A/C]CAGAGGGTATAAATT | 57690 |
rs533317164 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062705 | AAATGTTTTTTGTAC[C/T]GAAGTGTGAAGGGCG | 57690 |
rs533356450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042197 | GACTGTAAACCACTT[A/T]ACAGCAGAAGAAAAG | 57690 |
rs533359107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095765 | AAAGCACTAGCAGGC[C/T]GAGCACAGTGGCTTA | 57690 |
rs533367318 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002259 | AGCTGAGATTATATA[A/C]CAGAAATTGGTACCA | 57690 |
rs533369309 | snp | C/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104928 | AGACCCGCTGGAACC[C/G]AGCAGCGGCCGCCCT | 57690 |
rs533370044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088797 | TAAATAGTGCCTAGC[A/G]CATAGCAAACACTTT | 57690 |
rs533380196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010799 | ATTAATTTTTTTCCA[C/T]GGAAACAAAAAAAAT | 57690 |
rs533383522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023832 | CAAAAAAGCCTGGCC[A/G]GGCACTGTGGCTCAT | 57690 |
rs533386973 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108778 | TTCACCTGCATCTGT[A/G]GATATATATTTTTTT | 57690 |
rs533443310 | snp | C/T | 3.35576e-05 | 0.00409606 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102459 | TGTCAACCAGGTTCT[C/T]CCCTCTTGTTGCAGG | 57690 |
rs533444914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095032 | ACCTGGTGGGGCACC[A/G]GGGTTGTGCCAGACA | 57690 |
rs533509957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028947 | ACTTTACATGTCGGC[A/G]TGCAGAATTACTACT | 57690 |
rs533529135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024113 | CAAAAAAAAGCAAAA[A/G]CAAAAAAACCTTTTG | 57690 |
rs533540787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089537 | GTAAAGAAACCAGCA[A/G]CCCATGGTCAGTAGT | 57690 |
rs533599943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055728 | GCCTGGCACTGGAGT[C/T]GTGCAATAAATGTGG | 57690 |
rs533613246 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059102 | CCAGACTCCTGTCCT[A/G]GGAAGTTTATCATTC | 57690 |
rs533614830 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023396 | ATAGTTCTCTTTTTT[A/T]ATTCCTTCCTTCTCC | 57690 |
rs533616869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029701 | TTAGCTTAAAAGACA[C/T]ATTGCACAGCTGTAC | 57690 |
rs533635959 | in-del | -/ATTGAG | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002375 | GAAGCTCATAATCTC[-/ATTGAG]ATTTAAAGCCAGGAC | 57690 |
rs533657590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009924 | GGTCTAACTCTGTTG[C/T]CCAGGCTGGAGTGTA | 57690 |
rs533661446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036454 | ATGGAAAACTTACGT[A/G]TCCATTCCAGTAAAC | 57690 |
rs533680890 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033632 | CGAGATCACGCCATT[A/G]CACTCCAGCCTGGGT | 57690 |
rs533689408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055265 | AGACACAAACGCACA[C/T]GTTAGCCTAGGCCTA | 57690 |
rs533737973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062900 | CACATACTTTTTATG[C/T]CTTCAGAGTTTTATA | 57690 |
rs533750646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010970 | CGGGGCGCTGTGCTC[C/T]GGGGGCGCCTCCCGA | 57690 |
rs533764696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109043 | TTTTTGTAGAGATAG[A/G]GTCTCACCATGTTGC | 57690 |
rs533776882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056223 | AGTGCAGTGACACAA[C/T]CTCGTCTTACTGCAA | 57690 |
rs533792654 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090835 | ACTCTTTCAGAGCAG[A/C]CTTTTGTAAAGGAAA | 57690 |
rs533806186 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017005 | CCAAGGCCATACTTG[C/T]AGCTACTGCACTCCC | 57690 |
rs533816092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069874 | TGCATGCATGCACAC[A/G]TAGTGTATCAGCTTC | 57690 |
rs533834098 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016757 | TCTGAGAGGAGGAGG[A/T]TTATTATACTATAAA | 57690 |
rs533856229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069388 | ACCCACAGAAAGCCA[G/T]CGTTTTGATTTTTTT | 57690 |
rs533861722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063563 | ATGCTGTTGCAACAG[A/G]ACTTGGCAAAGGAAT | 57690 |
rs533898827 | snp | A/G/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010387 | TCACAAAGTATTGGC[A/G/T]GTGTGCTTAGGCTCA | 57690 |
rs533904058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077601 | GCTAACTTGGGACTG[A/G]CTAAAGTGATGATGT | 57690 |
rs533939891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076582 | TTATTTGCTAATCTG[A/G]CAACCCTAAATTGGG | 57690 |
rs533941414 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080135 | TCCCTTTTCAGGAGT[A/G]AACCATAGAGATTGT | 57690 |
rs533965340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043772 | ATCTTCATAAGTTCA[A/G]TTATGTTCGTTTTTA | 57690 |
rs533977796 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002523 | GCGATAATTTGTTTT[A/G]CTGATTTTTGTAAAT | 57690 |
rs534035951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095511 | ATCGTTTGACTTCCC[A/G]GGTGCTCGACGTTTG | 57690 |
rs534088267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065348 | AGCAAGACCCCATCT[C/G]TTTAAAAAGGAAAAA | 57690 |
rs534101207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041816 | TATCAACTGTTGAAA[A/G]CATTGCGAACTAGTT | 57690 |
rs534112341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055474 | GCATCACCACAAACA[C/T]GTGGGGAATGCATTC | 57690 |
rs534185014 | in-del | -/TT | 0.00795532 | 0.062565 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029794 | TTTTAACTTTTAAAC[-/TT]ATTAAAAACCTAGAC | 57690 |
rs534204476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071503 | CAGTCCTCCTGTCTC[A/G]GCCTCCCGAGTAGAG | 57690 |
rs534233847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030870 | TTAGGAGGCTGAGGC[A/G]AGCGGATCACTTGAG | 57690 |
rs534293133 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106011 | CAAGAAAATTATTAC[A/C]AGAGTATTGCACCAT | 57690 |
rs534324755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004807 | AGTATACCTATTAGA[A/G]CCTGTTAAAATTATA | 57690 |
rs534328773 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003240 | CATCCCATACATACA[A/G]AGCCCCTAATTGGTA | 57690 |
rs534334094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089703 | CATGTGATTCTTACA[G/T]GGCTCTAGAGAAGGA | 57690 |
rs534355950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057605 | AGCTTTCCATAGCTA[C/G]TGGGATTCCCAGACA | 57690 |
rs534387453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103331 | TGTTTAGTGTATCCA[A/G]TTTCATACGTTTTTT | 57690 |
rs534466071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104064 | TACTCCCTCCCTGTG[A/C]CACATTCCTACACAG | 57690 |
rs534469354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025293 | GTAGTTTTGCCTTCT[C/T]CAAAATGTCACGTAG | 57690 |
rs534482513 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028285 | AAGTGGGAACAAGGA[C/G]GTAGAGGGATTAGGA | 57690 |
rs534495618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032453 | TCAGCTTCTTTTCCA[A/G]TCTCCTTGACTTGAT | 57690 |
rs534591445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044616 | TAATAGTTATTGTTT[C/T]AATTGAGTTGGCAAG | 57690 |
rs534599169 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035006 | GCAGAATGGGAAAAT[C/G]TCTGAACCATAGGTG | 57690 |
rs534630848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051798 | TGGATACAGGAGCAA[A/C]GAAGATAGGATAGAC | 57690 |
rs534685671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020711 | GATATATCCAAAATA[C/T]CGCCATTTCAATGTG | 57690 |
rs534692764 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105797 | TGTTATTATTAGCTT[C/G]TAACTTTGCACTGAG | 57690 |
rs534759333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018826 | CTATAAACTAGAAAT[A/C]CAGGCCATAGATTGA | 57690 |
rs534768867 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027575 | GCCTTCATATCTACT[G/T]TGGAGAGAGTTGTGA | 57690 |
rs534785629 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076558 | AATGTAACTCAGCAT[C/T]GCATATGTTTATTTG | 57690 |
rs534790538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079756 | TTTCAGAGCTTGCTC[A/C]TTGGAATGCCTCAGC | 57690 |
rs534828988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026929 | AAATGACAAGGTTTG[A/G]TGATTGATTAGATGT | 57690 |
rs534918220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045958 | TCCTCTAACCCCATT[A/C]TGGTCCCCATCCCAC | 57690 |
rs534919773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038456 | AGGCAGGTGGATCAC[A/G]AGTTCAGGAGATTGA | 57690 |
rs534990804 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017346 | TCTGTTCAGACCAGG[A/G]TGAGGAATGTAAGGT | 57690 |
rs534999225 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027948 | TCGCCCAGGCTGGAG[C/T]GCAGTGGTGCGATCT | 57690 |
rs535023790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053198 | CCTGTTTACGTTAAC[C/T]GACTGGTTCCTTGGA | 57690 |
rs535033598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013875 | GAGGTGAGGCCAAAG[C/T]GAGAGATGGGGATTG | 57690 |
rs535146104 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066822 | CCTGTCGGGCCCAAC[C/T]TCAGGCCTGCCAGAC | 57690 |
rs535159876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033468 | TGAGGTCGAGAGTTC[A/G]AGACCAGCCTGACCA | 57690 |
rs535165679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034170 | GTGATTCTCCTGCCT[A/G]CCTCAGCCTCCTGAG | 57690 |
rs535181864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040105 | CATTGGCCTTCTCAT[A/G]AAATAATACAGGGGA | 57690 |
rs535197151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080584 | ATTTTACAATTTTAG[G/T]CTTTGGACCAAGTTT | 57690 |
rs535226976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007131 | ATTACAGGCGTGAGC[C/T]ACCGCACCTGGCCTC | 57690 |
rs535249740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054566 | ACTGTGGACTACTGC[A/G]CACCACTGCAGACTA | 57690 |
rs535272505 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101065 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAATTT | 57690 |
rs535342560 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060418 | TAAAAAGCCAAGCAC[A/G]TAGCAAGCACTCAAT | 57690 |
rs535350033 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019704 | TATTTCTTAAATAAA[A/G]CAAATGATTTGTTGA | 57690 |
rs535355799 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107772 | GGGACGGCAGCAAGA[A/G]GATGCCGGGGCTTGC | 57690 |
rs535356833 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052080 | CCCTGTGTCCAGCAG[A/G]ACAAGGGCACTTCAT | 57690 |
rs535373065 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106429 | TGTCTTGCACATGCC[A/G]GACGCGCTCTCAGGA | 57690 |
rs535379122 | snp | A/G | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108232 | GAAAAGATGGGACCC[A/G]CACCCCCGCCACAGG | 57690 |
rs535385544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099231 | GAGGATGGCTCAAGC[C/T]CAGGAGATTGAGGCT | 57690 |
rs535401908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074640 | CCCCCACATCTGGAA[A/G]AATACTTGCAGATAC | 57690 |
rs535413315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037924 | TAGTAATTTTAACAG[A/C]GTGTTTCTAGGGCAG | 57690 |
rs535413320 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004025 | AGTGCTGTTAGGGAA[A/G]TGTCCCTTTCTAGCA | 57690 |
rs535444621 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081279 | ATAGGAATTCTCGGG[A/G]GACGCAGACATTCAG | 57690 |
rs535471302 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015572 | CAGTGGTATACCTAG[C/T]TCATACCACATACTG | 57690 |
rs535543679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087522 | TTAAAGGTAGTACCA[A/G]TCAGAGCCCCCAAAA | 57690 |
rs535563340 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030674 | ATTATCATCAGAATT[A/G]AAACAAAAATACATA | 57690 |
rs535618375 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108324 | AAATTGAGAAGGAAA[A/G]CATTGAGTGGGACCT | 57690 |
rs535647944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076347 | CTGTGGGGTAGCCCA[A/G]GGTGAGGCTCACGTC | 57690 |
rs535677079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087855 | GCCTCGAGGTCAGGC[C/T]AGTCAGGAGAGACAC | 57690 |
rs535692587 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056226 | GCAGTGACACAATCT[C/T]GTCTTACTGCAACTT | 57690 |
rs535697846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022285 | GTCTGTCTTAGATAT[A/T]AGATTGACTACACAT | 57690 |
rs535780756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089023 | CCCAGGCTGGAGTGC[A/G]ATGGCGCAGTCTCGG | 57690 |
rs535781553 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028615 | ACATGGTAGATGGCC[A/C]AGTCCATGTTGAGAG | 57690 |
rs535859545 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017286 | GACTTGGGTGATTGA[A/G]TAAGATAGAAGCACC | 57690 |
rs535903269 | in-del | -/T | 0.275999 | 0.248644 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048154 | TCCTTGAGCTACAGA[-/T]TTTTTTTTTTTATTA | 57690 |
rs535978798 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015752 | CCGCATCTCTACTAA[A/G]AGTACAAAAATTAGC | 57690 |
rs535979820 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032039 | ACATTATTGGTCATG[A/C]GTTTGCAGATGGCAT | 57690 |
rs536026800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043915 | TTCTTTTTATGGCTG[A/G]ACAGTATTCCATTGT | 57690 |
rs536031507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069965 | TCGAGAGAACAGGAA[C/T]TAAGCAAATGGGGTG | 57690 |
rs536050736 | snp | C/T | 0.00114811 | 0.0239319 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104764 | GGGCCCGCCCAGCGC[C/T]GACGACAGCAGGGTG | 57690 |
rs536058183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075832 | GGTGTGACTGCAAAG[C/T]GGAGAAAAGCATTGC | 57690 |
rs536069181 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043302 | CCCGAGGCTGCAGCC[C/T]ATCCCAAGAAGTGCA | 57690 |
rs536110708 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096657 | CCGATTCTGTTTATG[G/T]TCATCAGTTTAGCAG | 57690 |
rs536119262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036551 | AAGTGGAATTTGTAG[C/T]GTTTTTAGCTGTGTA | 57690 |
rs536144595 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082414 | GTGTGTGCATCAGCA[C/G]TTTCTAACAGAGCCT | 57690 |
rs536166917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017917 | ATACTTTTTCAGGCT[C/T]TGCTTAATTGTCACT | 57690 |
rs536193946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010983 | TCCGGGGGCGCCTCC[C/T]GAGGGCACTTCTCCT | 57690 |
rs536224492 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094500 | CTGGAGTATAGTGGC[A/G]TGATCTTGGCTCACT | 57690 |
rs536224614 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102671 | AGGGTCCATAAGTGA[C/T]GCTGCATGGGAGGAG | 57690 |
rs536243923 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093984 | TTTATTATTATTACT[-/T]TTTTTTTTTTTTTGC | 57690 |
rs536262701 | in-del | -/CACTAGAC | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073390 | GACACTGGAACCACA[-/CACTAGAC]TTCAGTGGACACTGA | 57690 |
rs536339792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070654 | TTTCTTCTTGCTGCC[C/T]CTTTACTCATTGGAA | 57690 |
rs536350897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037845 | AGAAGAGCGAATGTA[C/T]GTGAATAGAAGAGCC | 57690 |
rs536417524 | snp | G/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012627 | AACTGCTTTATCTCA[G/T]CCAGGTGTCAGTAGG | 57690 |
rs536444539 | snp | A/G/T | 4.24962e-05 | 0.00460937 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051156 | CGGGGGGCCGGTACC[A/G/T]GTCAAACAGAAGGAC | 57690 |
rs536464346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090319 | CACAGTCCCCATGAA[A/G]CCCACTTCTTCATGT | 57690 |
rs536496507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058201 | CAAAGCTATTAAGTC[A/G]TCATAAAATCAGTCT | 57690 |
rs536502783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089802 | ATTGGATAGGATTAC[A/G]GTAAATAAAGAGGAA | 57690 |
rs536541940 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042840 | TAACAGTGGTGATGG[A/T]GGTGGTGGTGATGAT | 57690 |
rs536616551 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070404 | GAAGGGAATTTTTTT[C/G]ATATTGTAATAATGC | 57690 |
rs536629476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025451 | TAAATCACGTAATGT[C/T]CCATTGTCTGAATGC | 57690 |
rs536652474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071605 | GTTGGCCAGGCTGGT[C/T]TCGAACACCTGGGCT | 57690 |
rs536655482 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095928 | TGGTGGCACACGTCA[C/G]TGGTCCCAGCTACTC | 57690 |
rs536660839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085154 | TCTGCCACTAGATGA[C/T]GCTGCAGGCATTGCT | 57690 |
rs536720022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030971 | GGGCTTGGTGGCCTG[C/T]GCCTGTAATCCCAGC | 57690 |
rs536732607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005717 | CCACTCAGGAGTCAC[A/T]TAAACTAGCTCTGTT | 57690 |
rs536831012 | snp | C/T | 0.000116802 | 0.00764116 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097728 | CACCTTGCTCAGTGC[C/T]GTGTTTGGTTCTGCA | 57690 |
rs536852134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019649 | TTGCTGAAAGTTTTT[C/T]AAAATTATATATGTA | 57690 |
rs536852224 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080371 | GAATCGCTTGACCCG[G/T]GGAGGTGGAGATTGC | 57690 |
rs536902492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026701 | TATTCTGAGAGCGTT[A/G]CAAGACCTCAGAGTT | 57690 |
rs536914966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104107 | GTCCTCACAGCCAAC[C/T]CTTCACCCTAGTGAA | 57690 |
rs536937951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072851 | TTGAAAATCAAGTCA[G/T]TACATTTTCTTATTA | 57690 |
rs536939107 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029011 | TAAACCCTATTATTA[C/G]GTTATCACCCAACTC | 57690 |
rs536975883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086190 | CAAAAATTAGCTGGG[C/T]GTGGTGGCACACGAC | 57690 |
rs537013323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053882 | TTAAACAAACAAACA[A/G]AAAAGCTCCAGGAAC | 57690 |
rs537024391 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107546 | TGTCCCGCTGCATGC[A/G]TTCCCTCTGTAATTT | 57690 |
rs537025798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100159 | GCTTTTCCAGGCACA[C/T]GGTGCAAGCTGTCAG | 57690 |
rs537034983 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038886 | CTCATTTAATCTTCT[C/G]AAGACCCTGTAATCA | 57690 |
rs537046229 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080870 | GGGATCTTATGTTCA[A/G]TCTGTTCCAAAAGAG | 57690 |
rs537053169 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084743 | AAGCAATTCTCCTGT[C/G]TCAGCCTCCCGAGTA | 57690 |
rs537064801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014406 | GCTGTCTTGATTACT[C/T]AGCTTTAACATATGC | 57690 |
rs537067996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092362 | TGTATGAATTTTTAA[C/T]ATCCACTGTGTTCTT | 57690 |
rs537072209 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006530 | TCTTCTTCTTCTTCT[C/T]CTTCTTCTTCTTCTT | 57690 |
rs537106729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098960 | CTCCACAAGATGTCA[A/C]TGGGACGTAAGGCTT | 57690 |
rs537112649 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106627 | ATGTGTAGCAGTTAC[A/G]TATTTACCAAATAAT | 57690 |
rs537131431 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053295 | ATAAAGTACTTGGGG[G/T]GATAAGGAGAAGCAG | 57690 |
rs537149191 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105994 | TTTATTGTGGACTAA[G/T]GCAAGAAAATTATTA | 57690 |
rs537189884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012831 | GGTTGTGATTTATCT[A/G]TCTCACACTTTCTAC | 57690 |
rs537190960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021041 | ACCAACACAGTCCTG[A/G]ACTCAGACCAGGAAA | 57690 |
rs537195507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004991 | TAAACTTTCATAGAT[A/G]TGTACATTCTACACA | 57690 |
rs537212460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074131 | CTTCTTGAGCTTAGA[A/C]ACATGAGACAGCACC | 57690 |
rs537223774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034034 | CCCCAACATTTTCCC[C/T]GCCTACTCTCCATGG | 57690 |
rs537229831 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109002 | GGCATGCATGCGCCA[C/T]CCCACCCAGCTCATT | 57690 |
rs537366140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046916 | AAGTCCTCAAAGTAG[A/G]CCATTAACAAAGGGC | 57690 |
rs537376765 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014896 | AGCAGATGGACCCTC[C/G/T]GTACTCAGAGCTGTC | 57690 |
rs537377814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079205 | AGTGAGCCAAGACCG[C/T]GCTACTGCACTCCAG | 57690 |
rs537382367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093225 | AGAATCTGAGCTAAG[C/G]ATCTGGAAGCGTTAA | 57690 |
rs537393356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007465 | ACTTTCTGACTGGAC[A/G]CTTTTGTCGGGTGAC | 57690 |
rs537411185 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024929 | CTCCCGAGTAGCTGG[G/T]ATTACAGGTGTGCGC | 57690 |
rs537491317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060447 | ATAAATGCCTGATCG[A/G]TTGCATTTTTAATCG | 57690 |
rs537514243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028694 | CCGTATCATGAACCA[C/T]CCCCCAATGTTGACT | 57690 |
rs537520785 | in-del | -/GACTGGGAACTCGGGG | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108616 | GGTTGGATTTTGACA[-/GACTGGGAACTCGGGG]GACAGGAGGGCAGCA | 57690 |
rs537527992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059966 | AAACTGTATAAGATG[A/G]TTTTCCTTTTCTAAT | 57690 |
rs537536529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074721 | GCAGACAGAATAATC[A/G]GGAAGGCCCCTGCAA | 57690 |
rs537547060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041448 | TTTATTTAATAGACT[C/G]TTAACCTTGAGGAAG | 57690 |
rs537595806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028044 | GGGACTGCAGGCGCC[C/T]GCCACCATGCCCGGC | 57690 |
rs537610542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055397 | TAGTCTTGTATCAGC[A/C]TCATCAGTTGTGTGT | 57690 |
rs537687776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047870 | GCCAAAAAGTTGATC[A/G]AAATATAAGTTTGAC | 57690 |
rs537695636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054981 | GGACTACTGTACGCT[A/G]CCATACACCACTGCG | 57690 |
rs537700680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093875 | TACAAGGCACAGTTG[A/G]CGGGCACCTTTTCTA | 57690 |
rs537786829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100845 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 57690 |
rs537849855 | snp | C/G | 3.14431e-05 | 0.00396491 | missense | TNRC6C | GRCh38.p7 | 17:78075216 | ATGGCCGCCAAGCCC[C/G]TCGGCTGCCGCCCGC | 57690 |
rs537864860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082498 | TAGTAATAATTGCAG[C/G]AAAAGCTGGTTGCAA | 57690 |
rs537887612 | snp | A/G | 7.17463e-05 | 0.00598899 | missense | TNRC6C | GRCh38.p7 | 17:78050321 | GAACGGGAGAAGGCC[A/G]AAGGCGAGATAAAGG | 57690 |
rs537953385 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003371 | AGATATGCAGAAAAC[C/T]TAGAAGATTTTCAGA | 57690 |
rs537964026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088067 | GCAAAGGCCAGTTGA[G/T]TGGTAGTGAATTTGC | 57690 |
rs538016611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102173 | CAGAGCTTCCCTGGA[C/G]ATTCTCGGGCCTCAT | 57690 |
rs538021910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071251 | CATGTTTGTTATGTG[C/T]GTCAGAAGACACCAA | 57690 |
rs538057833 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093513 | CCTCTAATTTAATTA[C/G]CAGATTATAAAAATT | 57690 |
rs538100414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108948 | AGGTTAAGCTCCAGC[A/G]ATCTTCCGACCTCAG | 57690 |
rs538102427 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101654 | AGCAAGTCAGTCATT[A/C]GCATTGTTTCCGTAG | 57690 |
rs538139179 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108350 | GACCTAATCCGGAGA[A/C]GAAATTAAAGACCAG | 57690 |
rs538148247 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090566 | TCCCTTCCAAACAAG[C/T]AGTCTGTCCTGCTCC | 57690 |
rs538176680 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108499 | GGGGCAAACTGTACC[C/T]GTGCCTGTGCGCTGG | 57690 |
rs538179317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082937 | CAGTAGTTTCAGGGG[A/G]TCTCCCTACAAATTA | 57690 |
rs538224287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103979 | GGAATTGGGGAAAGG[C/T]GACACAGGTCAGTTC | 57690 |
rs538339518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064229 | GCCTCCCCAATAGCT[C/T]GGATTACAAGTGCAC | 57690 |
rs538376594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095268 | GTGAAGAAGATGGCC[C/T]GAGAAACACGTGACA | 57690 |
rs538387340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010368 | AGTGATGGAGGTTTT[A/G]GAGTCACAAAGTATT | 57690 |
rs538401166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025226 | AAATCCCCTGTGCTC[C/T]GCATAGTCATCCCCC | 57690 |
rs538405073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063765 | CTGCCATCTTCTCAT[C/T]TCTTTGCCCAGATAA | 57690 |
rs538424338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030840 | ATGGTGGCTCACACC[C/T]GTAATCCCAGCACTT | 57690 |
rs538457675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053832 | AGCCCAGGAGTTCAA[A/G]GCCTGCCTGGGCAAC | 57690 |
rs538494687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044526 | CTAGAATGTGTGCTC[C/T]ATGAGAGAAAGAAGT | 57690 |
rs538511216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030414 | GGTGATCCGCCCACC[A/G]TGGCCTCCCTAGACT | 57690 |
rs538528475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004776 | TACCTAGTTTAATGT[A/G]TCTTGTAGTTTAAAC | 57690 |
rs538546965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037187 | TTCACTCTTTTTCCT[G/T]TTCTTCCTATATGAG | 57690 |
rs538591062 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104990 | ACCTTGGCCGCAGTC[C/T]TTGCGAACTGTTCGC | 57690 |
rs538591614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012180 | TTTAGCATAACCAAA[G/T]ATTACATTAATAAAT | 57690 |
rs538631831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026757 | TCAGAAGGATCACAC[C/T]GGCTGCAGTATAGAT | 57690 |
rs538651454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096909 | AAGGGATTGAGGTGC[C/T]TTAAGGATGGCCCAT | 57690 |
rs538716910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032329 | AGCCCTGCTTCTTGT[G/T]GCTTCCTTGCCTGTA | 57690 |
rs538718896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026226 | AACACTATGCTGCCA[C/T]AATTTACAGCCTAGA | 57690 |
rs538771273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017316 | CTCAGCGTGCTCCCA[C/G]TCCTGCTCTCCTGCT | 57690 |
rs538806238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053176 | GCGCTGCTGTTCTTA[C/T]GCTGGGCCTGTTTAC | 57690 |
rs538840741 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072426 | CGACAGTGACTGACA[-/T]TAGTTGCTGGGACTA | 57690 |
rs538864544 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088403 | CTTTATTTTTCTTTC[-/T]TTTTTTTTTTGGTAG | 57690 |
rs538883009 | in-del | -/A | 0.0858192 | 0.188533 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013113 | CAAGCTATTCTACCC[-/A]AAAAAAGAGTTGAAA | 57690 |
rs538889749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052795 | GCTGCCACATCAGGA[A/G]TCCTTTATGGATCCT | 57690 |
rs538921857 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107762 | TCTGTTGTCTGGGAC[A/G]GCAGCAAGAAGATGC | 57690 |
rs538942663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043966 | TTATTCATCTGTTTA[C/T]GGACACATAGGTTGC | 57690 |
rs538958030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051685 | CACACTCAGTAGAAC[A/G]TCAAGCGAATGTTTT | 57690 |
rs538958687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090422 | AGCACCTGGCTAAGT[A/G]GTAGAGGCTCACTGT | 57690 |
rs538995800 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045970 | ATTCTGGTCCCCATC[C/T]CACCCCCAGAGGGAA | 57690 |
rs539007022 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076309 | TTGAGAGTCCTCCAG[C/T]ACGTGATCTGCCTCA | 57690 |
rs539017579 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080510 | ATATTGCTGTTTGGC[A/G]TGGCTCTGAGGCCTA | 57690 |
rs539021268 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103097 | TTGTCAGCAGCTGGA[C/G]CCAGGTGCCTTTTGC | 57690 |
rs539085421 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072649 | ACACTTTGGGAGCCC[A/G]AGGCAGGAGAACCAC | 57690 |
rs539094179 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039321 | CTTGCCCCCCCCCCC[C/G]ACTCCCTACCTCTTA | 57690 |
rs539116305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072236 | TCAGCGTGTCCTGAT[C/T]TATACTGTCTCAGTT | 57690 |
rs539125517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079058 | ATCGCACTACTGCAT[C/T]CCAGCCTGGGTGACA | 57690 |
rs539130488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038629 | GCTTGCAGTGAGCTG[A/C]GATGGTGCCACTGCA | 57690 |
rs539135384 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099112 | GAAACTGAAGATTTA[C/T]ACCAGCGTGGGCAAC | 57690 |
rs539153291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084893 | CGCCTCAGACTCCCA[A/G]AGTGCTGGGATTACA | 57690 |
rs539155162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086262 | TTGAACCCGGGAGGC[A/G]GAGGTGGCAGTGAGC | 57690 |
rs539177713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045837 | ATTTTTTCAATAGAA[G/T]AAAGTATATAGAAAA | 57690 |
rs539227276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013799 | AAAGAGCCTGTGGCC[A/G]TATGGAGTATGACAT | 57690 |
rs539227897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060648 | GTTGGCTAGGCTGGT[C/T]TCAAACTCCTGGCCT | 57690 |
rs539241145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021685 | AGTCATTATTCTGCC[A/T]CAGCCTCCCAAGTAG | 57690 |
rs539253362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074620 | TGTTTTGCACAGTAT[A/T]GTATCCCCCACATCT | 57690 |
rs539258594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099020 | CAGTTTGAAAAAACA[A/G]CTCTCATAATATTGC | 57690 |
rs539266394 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059895 | TGTGCCCCCCGCCAC[A/C/T]GATAGCAGTAGGAAA | 57690 |
rs539310268 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013247 | CCATTGGAGAGTTTT[A/G]AGTAGGAGAGTGACA | 57690 |
rs539412271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039978 | GTAGCCAAGGAGAGA[G/T]AGTCAGTTATTGCCA | 57690 |
rs539426616 | snp | A/C/T | 0.000549496 | 0.0165666 | missense | TNRC6C | GRCh38.p7 | 17:78086934 | CTGCTCGTGAAGCAG[A/C/T]CACCACCGCCACCGC | 57690 |
rs539449855 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051980 | TCCAGAGTAGAGAGA[G/T]TTTAAGGTGGCAAAG | 57690 |
rs539464986 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025080 | ACAGGCATGAGTCAC[C/T]GCGCCCGGCCAATAC | 57690 |
rs539509487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101011 | AAACTCCTGACCTCC[C/T]GTAATCCACCCATCT | 57690 |
rs539516480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092888 | TCTGGTGTCTCTCAA[C/T]TGGAGAGTATTCACT | 57690 |
rs539516826 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087582 | TTGTTCTGTTCCTAG[A/T]CTACTCTGAACTGTA | 57690 |
rs539531204 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057872 | GAATGCTACAGTACA[A/G]TCATTTTTGTCCTAT | 57690 |
rs539540622 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025139 | CATTAGGGTTCACTC[G/T]TTGTGTTATATATCT | 57690 |
rs539543254 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058892 | TTAAAACTTAGTTTT[C/T]TGAAACAATTATCAT | 57690 |
rs539577068 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071434 | AATGCTTTTTTTTTT[C/T]GGAGACAGGGTCTTG | 57690 |
rs539629379 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077599 | GTGCTAACTTGGGAC[G/T]GGCTAAAGTGATGAT | 57690 |
rs539717771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028097 | TAGAGACAGGGTTTC[A/G]CCGTGTTAGTCAGGA | 57690 |
rs539732763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034108 | GCCCAGGCTGAAATG[C/T]GATGGCACAGTTTTG | 57690 |
rs539764759 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040986 | CTCCCTGGCAGCTCT[A/C]CAGGAGGCGGCTCTC | 57690 |
rs539786243 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009394 | GATTAACTATGATAA[A/T]TTTCATAAATGTGAA | 57690 |
rs539822116 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053912 | CAGAATTAATACAGT[A/C]ATGCATAGCTTAACA | 57690 |
rs539823105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008428 | CTGCCAACATTCATA[A/C]CCCCATCCTACCCTG | 57690 |
rs539847546 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028137 | TCTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC | 57690 |
rs539887092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054477 | CTGCAGACTACTGCA[C/T]GCCACTGCAGACTAC | 57690 |
rs539904071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061220 | TTAATATCAGTATTT[C/T]AAATGTAAGAAATTT | 57690 |
rs539952587 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022848 | TGAAATATAAATGGA[A/C]AGTTGCATCTGTACT | 57690 |
rs540007947 | snp | C/T | 3.89552e-05 | 0.00441317 | missense | TNRC6C | GRCh38.p7 | 17:78075262 | CTTCCGTGGACCGCC[C/T]CACCTTTCTTGACAA | 57690 |
rs540029374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042469 | TATGGAAATACTTCA[A/G]ACTCCGAAATGGTAT | 57690 |
rs540035120 | in-del | -/A/AA | 0.544843 | 0.119066 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051480 | TGTTTCTTTACAAGT[-/A/AA]AAAAAAAAAAAAAAA | 57690 |
rs540079265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089142 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACT | 57690 |
rs540132838 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038589 | GAGGCTGAGGCAGGA[C/G]AATGCCGTGAACCCG | 57690 |
rs540153837 | snp | C/G | 1.68929e-05 | 0.00290623 | missense | TNRC6C | GRCh38.p7 | 17:78049241 | CCACAGGCTCCAGCT[C/G]TGGCCTGGCTCACTG | 57690 |
rs540158547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048706 | GACAAATAGCTTTTT[G/T]CTTTAAGTCATTTTT | 57690 |
rs540185509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009818 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 57690 |
rs540195696 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033775 | CATCTCAAAAAATTG[A/T]TCAATCTATGTAGTG | 57690 |
rs540202300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089953 | GAGAGATGGGTTGGC[A/G]CCAAATTGTGAAATT | 57690 |
rs540214762 | in-del | -/GG | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013794 | CTGTAAAGAGCCTGT[-/GG]GGCCGTATGGAGTAT | 57690 |
rs540216102 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094299 | AGTTTTATCACAGCA[A/T]GCTATTTTGTGGAAG | 57690 |
rs540234989 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062817 | ATTAGGGTTACCAAA[A/G]GTATAACTTAGGACT | 57690 |
rs540269767 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091241 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGGGAGG | 57690 |
rs540297524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015405 | TAAAAATGTCCCTCC[C/G]AGTTAGCATTTTTAC | 57690 |
rs540326935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076091 | CATGGTGGCACACGC[A/C]TGTGAACCCAGCTAC | 57690 |
rs540382666 | in-del | -/A | 0.0107246 | 0.0724382 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108260 | GGCTGGCCCCCCCCC[-/A]ACCCATGGGGAAGGT | 57690 |
rs540394159 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074215 | AGAAATACGAAAAGC[C/G]TGGCAATAAATGGAC | 57690 |
rs540408420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082575 | CAAATTCTCAGAAGG[A/G]AGTATGCCTTAACCC | 57690 |
rs540446064 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082194 | GCTGGGTCCGGGGGG[G/T]CACCGCCTTCTGATC | 57690 |
rs540481822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088522 | ACACCATACTGAGCC[A/G]TGCCTTAATTTCTTC | 57690 |
rs540541418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102796 | CCAGAGGCTGGAAAA[A/G]TGTGCTCTGTAAATA | 57690 |
rs540549414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063817 | TCAAAAGATAAACAA[G/T]AATAATATTTCAGTA | 57690 |
rs540578437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094811 | AAGCCAACATAAGTA[C/G]AGATTGCCCTTTCTG | 57690 |
rs540584500 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062974 | GTAAAGACTGGGTAC[A/G]GTAACTCACATCTGT | 57690 |
rs540608589 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024382 | TGTTTGTTTGTTTTT[C/T]TGGAGATGGAGTCTC | 57690 |
rs540613677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109248 | GCCAGCAGACACAGA[A/G]GCATCATGGCGAGCC | 57690 |
rs540696152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030138 | ACTACTGTACATAAT[C/G]TATGTGCTAGACTTT | 57690 |
rs540857522 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005400 | AGAACAACCAAAGGA[A/T]ATCTGCATTTTTTTA | 57690 |
rs540860953 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025489 | TATCCATTCACGTAC[C/T]GAAAAACATCTTGGT | 57690 |
rs540893221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025673 | ATATATTTATATTTA[A/C]GAATCAACTTCAACT | 57690 |
rs540898544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055756 | TGGTCTGGCCATGGT[G/T]GGCAGTCATGTATGG | 57690 |
rs540902375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017420 | GTGGCGGAGCTGAAC[A/C]AGGAGGGCACCGCTG | 57690 |
rs540938979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024950 | AGGTGTGCGCCATGA[C/T]GCCCAGCTAATTTTT | 57690 |
rs540968519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031107 | CACTGTCTCACACTT[A/T]AAAAAAAAAAGAAAG | 57690 |
rs540979138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044924 | TGTCCATGGATTTGA[A/G]ATGGGAAAAAAGAAT | 57690 |
rs541005150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077900 | GTTGTTTGCCACTTC[A/G]TCTCACTTTTCTCAT | 57690 |
rs541025251 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080671 | ATAACATCTTTGCTG[C/T]GTGGGGTAACTCAGG | 57690 |
rs541057452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044042 | GCTCTCTCTTCAATA[C/T]ACTGATCTCCTTTCT | 57690 |
rs541078978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005155 | GATGACTTTTTTTTT[A/T]AAATTGATGGTTAAA | 57690 |
rs541101454 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013531 | TGGTACTGTGCTGAT[C/T]GCTATGGGAAGAAAA | 57690 |
rs541145487 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051357 | CACCACCACCACCAC[C/T]ACTACCACGAGCAAC | 57690 |
rs541172844 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104355 | GTCTGGGTTTGGAAA[A/T]AGCAGTGGCAAAACA | 57690 |
rs541219490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039444 | GCGTTATTGATGTCA[A/G]CAAGTATCCCATTTT | 57690 |
rs541229135 | snp | C/T | 3.90678e-05 | 0.00441955 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064967 | CTGCTTGCCCTGATC[C/T]GGCAATTTGGAAATG | 57690 |
rs541285349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031887 | TTGATCTGAAAACTT[C/T]GCTATTTTCAACTTT | 57690 |
rs541315572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085754 | CACATTATTATTGAA[C/T]GATTTGGGACAGTTA | 57690 |
rs541339397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045470 | TACACCTCAAAGCCC[A/G]GGAAGGTCTGAGTAG | 57690 |
rs541391938 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074057 | GGCCAACAGTGCTTT[A/G]ACTCGTGCCTACATG | 57690 |
rs541403296 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032190 | TTCTCTCAATTTCCT[A/G]GTCTGTCTTATGAGT | 57690 |
rs541416203 | snp | C/T | 0.000100563 | 0.00709024 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091483 | CAGCATGGACATGAC[C/T]GGTGGCTTGTCGGTG | 57690 |
rs541452484 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106197 | TGGGCTCCCACCTGT[G/T]TACAGACCTTTTTTT | 57690 |
rs541516198 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046154 | ATTTCTGGTTGGGTT[C/G]TTGGCCTCTTTCTTA | 57690 |
rs541523059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073765 | GTTTTTCTGTTTCAA[G/T]ACACCTTATTTAATA | 57690 |
rs541564985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027295 | GGAGAATGTGGAGTC[C/T]AGGAGAGGTGATTGT | 57690 |
rs541606242 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101191 | TGCCAGATACCCTCA[A/G]TCATCCCTCTCAAGT | 57690 |
rs541613046 | snp | C/G | 0.00014907 | 0.00863207 | missense | TNRC6C | GRCh38.p7 | 17:78087006 | GCCATGGACAGCTTC[C/G]CCTCGCACCCACAGA | 57690 |
rs541734153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053498 | GCCGGGCATGGTGGC[A/G]CATGTCTCTAATCCC | 57690 |
rs541759373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006046 | TAATACTATGCTTTT[A/G]TGAGACATTTTATAA | 57690 |
rs541762824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099659 | GAGTTACAATTCAAG[A/G]TGAGATTTGGGTGGG | 57690 |
rs541786770 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091938 | TGTTTTCAATAAAAT[A/G]GTAAAACATAAATAG | 57690 |
rs541823422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021256 | TCCAGGGCTGGAGAA[C/T]GAGTACAAAGACTTG | 57690 |
rs541889172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034551 | CCATTCTGTTCTCAC[A/G]GGTGTAATATGCCCA | 57690 |
rs541908031 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081070 | CCAAGATCAAGGTGC[C/G]AGAAGATTCAGTGTC | 57690 |
rs541941870 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032871 | AGTCTCTTCAAATAG[G/T]CTTGGCTTTCGTCTG | 57690 |
rs541956672 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009623 | GCAGTGGTGCAATCT[C/T]GGCTCACTGGAACCT | 57690 |
rs541998246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023576 | TTGAGAGGCTGAGGT[A/G]GATAGACTGCTTGAG | 57690 |
rs542008492 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108627 | GACAGACTGGGAACT[C/T]GGGGGACAGGAGGGC | 57690 |
rs542017376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007690 | ATAGGAAAGTGTTTA[C/G]CAATTTGAGAGAGTC | 57690 |
rs542084030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022976 | TAGGTATTATAAGTA[A/G]TCTAGAGATTATTTA | 57690 |
rs542084353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060756 | ACCTTTTAACTAAAA[C/T]TTTCCTCCCAAAAAG | 57690 |
rs542085395 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108113 | CCTCTGAAGACAAAC[C/T]GAGCACCCCAGCGGC | 57690 |
rs542179381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014144 | CACATTTGAGACATA[A/T]TTCCACTTAAATCTT | 57690 |
rs542224353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010538 | TACAACCACATAATG[A/G]GGCTGGAGACATGAG | 57690 |
rs542270393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78041038 | GTAGCGAGAGGCCAG[A/G]CGAGCCTCGATGCAG | 57690 |
rs542298483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100279 | TCCAACCCCACATTT[C/T]CCTTCCACACTGCCC | 57690 |
rs542325431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102365 | GCTTTCCTAAAGCAC[A/G]CAGTGACGGCCTGTG | 57690 |
rs542358258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040531 | GGCTCATTTAGAATA[C/T]TACAGCTAGTGTTGG | 57690 |
rs542399215 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029711 | AGACACATTGCACAG[C/G]TGTACAAAAAATATT | 57690 |
rs542405932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037320 | TTCATTGAGCAGAAC[A/G]TTTGTTGAATGCCTA | 57690 |
rs542442275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069444 | GAGTCTTGCTGTGTC[A/T]CCTTAGGGGCTGGAG | 57690 |
rs542515059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028866 | CAAAATAGATGTAAT[A/G]TCCTGGATAATGATG | 57690 |
rs542528579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042551 | GCTGCTCTTAAAATT[C/T]GGTCATTTCACAGAT | 57690 |
rs542530087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068778 | GCACTCCAGCCTGGG[C/G]GACAGAGCGAGACTC | 57690 |
rs542544918 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099500 | CAAGAAGAGAGAGAG[A/C]GCTTGTGCAGGGAAA | 57690 |
rs542569481 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038904 | GACCCTGTAATCACC[A/G]CAGGCGACCAGCGAG | 57690 |
rs542586239 | snp | G/T | 1.70545e-05 | 0.0029201 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064677 | ATTTTTGCTTTTCTC[G/T]GATGCACTTTCATTA | 57690 |
rs542586398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056762 | GAGCCACCACGCCTG[A/G]CCCAGAAACTACTTT | 57690 |
rs542603786 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002691 | TGAGGCCAGGAGTTC[A/G]AGACTAGCCTGGACA | 57690 |
rs542623106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063919 | CAAGCTATTTAACCA[C/T]AGTTTTAAACTATTC | 57690 |
rs542656189 | snp | A/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78049280 | GTGGTGGGGATGGAA[A/G]AATGGACACTATGAT | 57690 |
rs542707751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101846 | CCTTGCCCTCATTCC[A/G]GTACACCCACAACCT | 57690 |
rs542724169 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025000 | GGTTTCACCATGTTA[A/C/G]CCAGTGTGATCTCAA | 57690 |
rs542759020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030560 | TCCATTATAATCTTA[C/T]GGAACCACTGTCATA | 57690 |
rs542777064 | snp | C/T | 0.000149615 | 0.00864783 | missense | TNRC6C | GRCh38.p7 | 17:78049969 | TGGGATTCAGGACCT[C/T]CTGCTGGTCCTGGAA | 57690 |
rs542798718 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014575 | TGAAATGATTCTTAC[C/T]GTTTGTAGTCATTAT | 57690 |
rs542810671 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085034 | GCTTTCAGTCCTGCC[C/T]GCCGGAGACCACTGA | 57690 |
rs542822179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076254 | AAAAAAAGGAAAGGC[C/T]CACAAGCAAAGAATA | 57690 |
rs542845873 | snp | G/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010479 | GCATATCTTCCCAAT[G/T]TTATAGTCACACATA | 57690 |
rs542857508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083282 | GGGATGTCATTGAGA[C/T]TCTCATGAAGTATTT | 57690 |
rs542865953 | in-del | -/AG | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031121 | TAAAAAAAAAAAGAA[-/AG]AAAGAAATGCATATT | 57690 |
rs542900073 | snp | A/G | 0.000409249 | 0.0142988 | missense | TNRC6C | GRCh38.p7 | 17:78051388 | ACCACACACAGGGTC[A/G]AGACGCCGCCCCCGC | 57690 |
rs542901176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057666 | GTTTCTGCTATTTTT[A/G]AAGTTGGTGTTTTTA | 57690 |
rs542907171 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008061 | TTAACTAGTCTAATC[C/T]GTTCTTAATAGATGA | 57690 |
rs542916409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097169 | CTGTGCACTGTGATC[A/G]TGCCTGTGAACAGCC | 57690 |
rs542950854 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013074 | TAAACCCGTCCATCA[G/T]GTCATTAAAACTGAG | 57690 |
rs542953124 | snp | A/G | 0.00011634 | 0.00762604 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103587 | ACCTCAGCGCTCCAA[A/G]TAGCTCCCCATCCCC | 57690 |
rs542982220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089331 | TTCATGCAGTGAATC[G/T]TTGAAATTAGTTGAA | 57690 |
rs543030067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021822 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 57690 |
rs543068961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084542 | TATGTGTCCTCGCTT[C/T]AATGGAAAGCACAGA | 57690 |
rs543114115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024461 | AAGCTTCGCCTCCCA[C/G]GTTCACGCCATTCTC | 57690 |
rs543150243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091321 | TCAAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 57690 |
rs543155974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084129 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCGGGC | 57690 |
rs543186343 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080913 | CATCAATCTTCTATT[A/G]TTCATAAAATTTAAT | 57690 |
rs543201661 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105181 | GGGCACTTTTCAGAT[C/T]GTGGGCTGGAAAGGG | 57690 |
rs543359536 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025894 | ATCACAGAATTAAAA[C/T]TGCATGTCATGTTCT | 57690 |
rs543414721 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056260 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 57690 |
rs543476536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031129 | AAAAGAAAGAAAGAA[A/G]TGCATATTCCCAGTT | 57690 |
rs543476792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038499 | TAACACGGTGAAACC[C/G]CATCTCTACTAAAAA | 57690 |
rs543480957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006126 | AACAGGAAAGGAATT[C/T]GTTTACAGATAATCT | 57690 |
rs543500632 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045513 | TAGTGGAAGTGGTTC[A/C]CTCAGAAGATGGACG | 57690 |
rs543516909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092078 | CCCATCGGGAACTCT[C/T]TACTGATGGACACAC | 57690 |
rs543542532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013466 | AGAAACTAACTGAGC[C/T]AACTAATCATTTGAT | 57690 |
rs543549080 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103959 | GGTGTTAGGACTTCA[A/G]CAAAGGAATTGGGGA | 57690 |
rs543615687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059429 | GAGTTGGGAGCCTGC[C/T]ACGGAAGTAGGAAGA | 57690 |
rs543651383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027934 | TTTGAGATGGAGTCT[C/T]GCCCAGGCTGGAGTG | 57690 |
rs543671633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073817 | GTGTAACATTTTTCT[A/G]ACCCTGGATAATGTG | 57690 |
rs543676022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073416 | AGTGGACACTGAGTG[C/T]GTTCCTCGTGCCTTG | 57690 |
rs543691554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073262 | CCACAGAGGGAGCCT[C/T]TTGGGATTAGCGGAC | 57690 |
rs543729232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039645 | GTTAATGCTGTGGCT[G/T]TTGTCAGGCAGCATC | 57690 |
rs543738482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065773 | AATTTTAAAAAGGTA[C/T]ATTTTCCTCCCATTT | 57690 |
rs543775739 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054247 | GGAAGTGGCTGTGGG[G/T]GAGTCAGTGAGTTAG | 57690 |
rs543776591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092620 | CATGGTGGCTCACAC[C/T]TGTAGTTCCAGCTAC | 57690 |
rs543813900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060791 | GCCCATCACACTTAT[A/G]AAGCTATGTAAGTGG | 57690 |
rs543819223 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085811 | TGTCCTGGACTTCAG[A/T]CTCCATCATTATAGA | 57690 |
rs543839644 | in-del | -/CT | 0.0331136 | 0.124339 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039319 | TCTTGCCCCCCCCCC[-/CT]CCACTCCCTACCTCT | 57690 |
rs543844121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022441 | TAGCATGAACTCCTT[C/T]TCCTCTGAAGGTTTT | 57690 |
rs543862534 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78004179 | TAATAGGGAGAAAGA[A/G]CAAGAAACACAAGAA | 57690 |
rs543868407 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068633 | ACCCCATCTCTACTA[A/G]AAATACAAAAACTAG | 57690 |
rs543926319 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017859 | TGTAGGTACGAGGTG[C/T]GCACACATACACACA | 57690 |
rs543978520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021374 | CTGATGTGCTTGTGC[G/T]CGTTCACTGGTCCTG | 57690 |
rs544038591 | snp | A/G | 3.38564e-05 | 0.00411425 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049182 | TGCCCTTGGAGCAGG[A/G]GGAGCGAACAGTAAT | 57690 |
rs544054281 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106354 | TGTTCCCTCGGCCAT[C/T]GTCGTGGACTCTGTC | 57690 |
rs544054905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094720 | GCTGGGATTACAGGC[A/G]TGAGCCAGTGTGCCT | 57690 |
rs544149725 | in-del | -/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105114 | TGTTGTCATTTTGAT[-/T]TTTTTTTTTTTTTTT | 57690 |
rs544214204 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107835 | TTGCCTAGGGTCCAG[C/T]TGGGGCTTAAAAAAT | 57690 |
rs544342089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081597 | TACAGTGCAGAAAGA[A/C]GCAGTGCAGGGATCG | 57690 |
rs544430142 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065905 | TTGTAATATTAACAT[A/G]AGTATAAGATTACTG | 57690 |
rs544433027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035712 | CATCACTCTGTGATT[C/T]GTGTATATTTTGAAG | 57690 |
rs544444182 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094101 | TCTCCTGCCTCAGCC[A/T]CCCAAGTAGCTGGAA | 57690 |
rs544460332 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094207 | GGCTGGTCTCGAACT[A/C]CTGACCTCAGGTGTC | 57690 |
rs544487504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008706 | GGTTGTTGTTGTAGT[C/T]AACTTTTTCTTATTT | 57690 |
rs544512608 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108706 | CGTGGGCCTGGGTGT[C/G]CAGGGCACCATTTCC | 57690 |
rs544517974 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086392 | CAGTATGGGCCAAGA[A/G]GAGTGGCTAGGTTCT | 57690 |
rs544534918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075993 | AGGCTGAGGTGGGTG[C/G]ATCACCTGAGGTCAG | 57690 |
rs544538980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088009 | AGTCTGTAGATACAG[A/G]ACAAAGGGTTATCGG | 57690 |
rs544543872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078686 | AAATTCACTTGGGGC[C/T]GAACGAGGTGGCTCA | 57690 |
rs544547695 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024355 | AGAGCAGTTTTTTTT[G/T]GTTTTTTTGTTTGTT | 57690 |
rs544548688 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007752 | CAGTTATAAATTAGA[C/T]TGCATAATATACTGA | 57690 |
rs544578124 | in-del | -/TTTTGGAAATTGAGA | 0.00119832 | 0.0244484 | cds-indel, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108303 | GCTCTGACCATACTC[-/TTTTGGAAATTGAGA]AGGAAAGCATTGAGT | 57690 |
rs544603555 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086286 | AGTGAGCTGAGATCA[C/T]GCCATTACACTCCAG | 57690 |
rs544610363 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003521 | GGATTAGAAGATCAA[A/G]TTGAATCAAGCACCC | 57690 |
rs544611728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075433 | TTATGAACATTTAAC[C/T]CAAAGAAGGGAATGT | 57690 |
rs544671790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011204 | CTTTATTGAGTTATT[A/G]TGGACATTATATTTA | 57690 |
rs544672031 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002792 | AGTCCCCACCTCCCT[C/T]CATCCTTGTTTTTGT | 57690 |
rs544699083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089846 | AAGGGGAAGCCTCAC[A/G]TAGCACAGAAGAAAG | 57690 |
rs544733336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010660 | AGAAATTGATTGTAT[A/G]AGGTATCTTTAGGGG | 57690 |
rs544736902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035254 | ATCAGCAAGCATGGA[A/G]GCAGTATGGCAAAGT | 57690 |
rs544752016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102711 | TGCCAGGATTGGCTC[C/T]AGCAGCGGCAGCAGA | 57690 |
rs544791773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055606 | CAAACCGTCATTATG[C/T]AGCCCATGACTATTT | 57690 |
rs544798522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031043 | GGTGGAGGTTGCAGT[G/T]AGCTAAGATGGTGCC | 57690 |
rs544805272 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033529 | ACAAAATTAGCTGGG[C/T]ATGTTGGCACATGCC | 57690 |
rs544860551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016181 | TGACTTCTAGAGCAC[A/G]GTGCCACTGCCGCAG | 57690 |
rs544861245 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056535 | GTGGCACAATCTCAG[C/G]TCACTGCAAGCTCCG | 57690 |
rs544889228 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018376 | CTCGTGATCCGCCCC[A/G]CCTCGGCCTCCCAAA | 57690 |
rs544916875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062634 | GAGCTTATGGCAGAA[A/G]CAAAAGATTAGAATT | 57690 |
rs544919957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069562 | CTAATTTTATTTTTT[A/T]TTTTTTCTGTAGAGA | 57690 |
rs544927467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030033 | TTTTATGTAGAAGCA[A/G]TACACTCTAAAATAA | 57690 |
rs544999362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037347 | CCTACCAAACATCAC[A/G]TACCCTGCACTGGGG | 57690 |
rs545027375 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011101 | ACAAAGTTACAGTTT[A/G]TAACTCTAAAGGATG | 57690 |
rs545032291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042702 | TGATGGTGATGATGG[A/G]GTTGGTGATGATGGT | 57690 |
rs545066452 | snp | C/T | 0.000127214 | 0.00797438 | missense | TNRC6C | GRCh38.p7 | 17:78050651 | ACAGCAACAACAAAG[C/T]GCCAAGTGGCCCGGG | 57690 |
rs545087291 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043513 | GGCATGCAATGTGTA[A/G]TAATCACATCAGGAT | 57690 |
rs545103971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066453 | TTTTTTTACAAACCT[A/G]AAGGATAAGGGAACT | 57690 |
rs545107479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025551 | CTGCTATAAACATTT[A/G]TGTGCAGGTTTTTGT | 57690 |
rs545108376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056493 | TTTTGAGACAGAGTC[C/T]TGCTCTGTTGCCCAG | 57690 |
rs545189964 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095766 | AAGCACTAGCAGGCC[A/G]AGCACAGTGGCTTAC | 57690 |
rs545195039 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070942 | ACTGTTAGGGAGTTT[C/G]TGGAATACAGCATTA | 57690 |
rs545202621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071680 | GGCATGAGTCACTAC[A/G]CCCAGCCGGAAAATG | 57690 |
rs545211392 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059981 | GTTTTCCTTTTCTAA[C/T]ACTTCACATGATGAC | 57690 |
rs545231529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038524 | TAAAAAAAAAAATAC[A/T]AAAAATTAGCCGGGC | 57690 |
rs545292601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084608 | TCAGAGACTGTTTTT[A/T]CTTTTTCTTTTTCTT | 57690 |
rs545317102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076706 | GTAGATGTTAAAAAA[A/T]AATTAATAAGGTTCT | 57690 |
rs545363799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073725 | CATTTTTGTCAACCA[A/G]TCAATATATAACCTT | 57690 |
rs545392718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065597 | GCAAGATAGATAAAA[A/C]ATGTCATCTCCTTGA | 57690 |
rs545397648 | snp | A/G | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109135 | GTTGTTGTTGCTGCT[A/G]TTTTGGCAACATCAC | 57690 |
rs545426341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065244 | GTAATCCCAGCTATT[C/T]GGGAGGCTATGGTGG | 57690 |
rs545514816 | snp | C/T | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093663 | ACTGCAGAATATTGA[C/T]CCTGAGAATGACCCT | 57690 |
rs545517577 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070515 | CCCCACCCCCACTGC[C/T]CTTTCTGTAGCTGAC | 57690 |
rs545527352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078923 | TGGTGAAACCCCGTC[G/T]CTACTAAAAATACAA | 57690 |
rs545540605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045339 | ATGGCATCCTATATG[A/G]CCATCCTTAGGGCAC | 57690 |
rs545579644 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026557 | TAGAATTGATGAAAT[G/T]TGGTGGTTAGATGAA | 57690 |
rs545606127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091749 | CCATTCCATTATAGT[A/G]CATATAAGATCTCAG | 57690 |
rs545664130 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106066 | AAGAGAAAAAAAAAA[A/C]AAACTGTTGTTGAAC | 57690 |
rs545682954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005048 | TTTCTCTCTCTTTTT[C/T]TTTTTTCAGGCTGCT | 57690 |
rs545731202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013508 | TTATTGAGCACCTGC[C/T]ATTTGCTTGGTACTG | 57690 |
rs545744575 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004141 | AACATGATCATCAAA[C/T]TTATACTAGTTTTCT | 57690 |
rs545758319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015807 | ATCCCAGCTACTCGG[A/G]AGGCCAAGGCAGGAG | 57690 |
rs545759658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059492 | CGTGTGAACCCCACA[C/T]GCAAAGGCCTTAGCT | 57690 |
rs545790143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020311 | GCTTGCATTATACTC[C/T]GGGACCCTTGGTCTT | 57690 |
rs545801108 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035455 | TGTTGAGTAATGCAG[A/G]TGATAGTTGTTAGTG | 57690 |
rs545812002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027100 | AATAGTGGCATAGAG[A/G]AGAAGGCAGGAGTGG | 57690 |
rs545820691 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029386 | CAGCATGTTACTATA[C/T]TGAATACTGTAGGCA | 57690 |
rs545858929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007607 | CCAGATTGTGTGTCT[A/G]TGAGGGCAGGGGCCA | 57690 |
rs545890825 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059963 | TCAAAACTGTATAAG[A/T]TGGTTTTCCTTTTCT | 57690 |
rs545906721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039678 | GTGGCTGCCATCCCT[C/T]GTGGGAAACACAGGC | 57690 |
rs545916736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085313 | ATTTTAAAACAATGT[A/G]TTCTGTTCTTAAATT | 57690 |
rs545984212 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028756 | AAGGTATGTACAGAA[A/C]TAGGCATAAACTCAT | 57690 |
rs546022930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028192 | GAGCCATCGCCCCCC[A/G]CTGAAACTTGGAGTT | 57690 |
rs546050934 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021183 | GGGACAGTACTCAGG[C/T]ATCAGTAGCACAGAA | 57690 |
rs546061048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067046 | TTTATGAAGCATCCC[A/G]TATACAAATTTTCCT | 57690 |
rs546089343 | snp | A/G | 6.95894e-05 | 0.00589829 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067944 | TACAACACTCTTAAC[A/G]ACGGTACACCCTGAA | 57690 |
rs546103756 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043890 | TGTTGTTGCAAATGA[C/T]AGGATCTTATTCTTT | 57690 |
rs546116007 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035085 | TCTCATCTAAAATGA[C/G]AGGTTTGAACCTCTC | 57690 |
rs546131053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027674 | TGCCTCTCTGACCCC[A/G]TTGATTGTGAGACAT | 57690 |
rs546198178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087150 | GGGTACCTGGAGTCC[A/G]TATGTGGTAGCCAGG | 57690 |
rs546231095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047606 | AAAAGAGAATTTATG[A/T]GGGAAATTCATGTTT | 57690 |
rs546297314 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092414 | AAAAGGAGGGAAGAG[A/G]TAACAGCAAATTTGA | 57690 |
rs546302750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053940 | ACAATGGTGATACAT[A/T]CTAAGAAATGTGTCA | 57690 |
rs546382762 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085539 | TGTTGTAAGAAAAAA[A/C]ATCATGATATTCAAC | 57690 |
rs546419587 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082868 | TCTTTACACAGTCCT[G/T]CATGCAATTTTGTAT | 57690 |
rs546503796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035569 | CAGCTACCTGACAGG[C/T]TGAGGGAGAAGGATC | 57690 |
rs546509460 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081327 | GGCAATGCTAGCATA[C/T]GAAAAAGAGCAGGAT | 57690 |
rs546538277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081633 | GACTCTGCCATAGCC[A/G]CTTCCCAGGAACAGG | 57690 |
rs546552284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080968 | TATGGTGTCTTAGTC[C/T]ATTTGGGCTGCTGTA | 57690 |
rs546559640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087490 | CCGCTGCCAATAATA[C/T]TCTCAGTATAAAACC | 57690 |
rs546580460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102075 | TTAGCGGCAGCCTTC[A/T]GGGATTTGCTCTGTT | 57690 |
rs546595680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041332 | CGCACGGAGCAGAGA[C/T]TTACCCATGGCTTTC | 57690 |
rs546622644 | snp | C/T | 1.88159e-05 | 0.00306718 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104623 | CCAGCCGCGGCTCAG[C/T]GCAGCGGGCAGCTCC | 57690 |
rs546626240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087900 | AAGACACCAGAGGGT[A/G]TAAATTAGTAAATTG | 57690 |
rs546630832 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089595 | CATGTTCAGCCTGTC[A/G]TTGTTATTCTCAGTC | 57690 |
rs546636128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063801 | TCTGTGTCTATGATG[A/G]TCAAAAGATAAACAA | 57690 |
rs546653107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016233 | CTAACACTGTCTCTC[C/T]CAGCCACAAAAGGAG | 57690 |
rs546679598 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062706 | AATGTTTTTTGTACT[A/G]AAGTGTGAAGGGCGT | 57690 |
rs546680472 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060507 | GACAGAGTCTTAACT[C/G]TGTCGCCCAGGCTGG | 57690 |
rs546727820 | snp | G/T | 1.94222e-05 | 0.0031162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092896 | CTCTCAACTGGAGAG[G/T]ATTCACTCGCTTCTT | 57690 |
rs546800839 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002963 | AGTCAGGAAATGGGA[A/C]GATTCAGTGAGGATC | 57690 |
rs546805113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028963 | TGCAGAATTACTACT[C/T]GAATCACTGTTTGCA | 57690 |
rs546812053 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021673 | CTCCCTGGCTCAAGT[C/G]ATTATTCTGCCTCAG | 57690 |
rs546857220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089540 | AAGAAACCAGCAGCC[C/T]ATGGTCAGTAGTGGG | 57690 |
rs546863962 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002280 | ATTGGTACCAGAAAT[A/G]CCCTGAAGAGTAACA | 57690 |
rs546882081 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069640 | TTGTAGTAAAAAGAT[-/AAC]AATAATTTATGTGTA | 57690 |
rs546887430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034884 | TGAGGTGGGACAATC[A/G]CTTGAGTCTGGGAGG | 57690 |
rs546892629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095045 | CCAGGGTTGTGCCAG[A/T]CAGGAAAATTAGCAT | 57690 |
rs546899380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037574 | AGGTGAAAGGGCGTC[A/G]CAGATGGAGTGACCT | 57690 |
rs546909249 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068960 | AGGTCACAAACTTAA[A/G]TATTAAAAATATGAA | 57690 |
rs546919144 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087445 | AATAAGGGAACAACA[C/T]TAACCACGTTGTATA | 57690 |
rs546945853 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018582 | ATTGCATGGGAAAAC[A/G]ACGAGTTTGAGCCCT | 57690 |
rs546946260 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066656 | GAAAATTTGGGGTAA[A/T]TTTGATACCGAAAAT | 57690 |
rs546961790 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052473 | TCTAGATCTAGTGAG[C/G]GTGGCAAACAACACA | 57690 |
rs546975543 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054881 | ACACCACTGCAGACT[A/C]CTGTACGCTACCATA | 57690 |
rs547035571 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015709 | CTGAGGTCAGGAGTT[A/C]CAGACCAGCCTGGCC | 57690 |
rs547060360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061949 | CTATTGCCTTCTCAA[A/G]GAGATGGAGGTCTAG | 57690 |
rs547111310 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018661 | ATGTATCTTACTTAC[A/C]CATCAAGTTTATTAT | 57690 |
rs547116062 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023185 | ATGCGTAGGTTATAC[A/G]CAAATAATAACCTGT | 57690 |
rs547127709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036498 | AGATAAAATTAAACA[A/G]TAGAGGAGCAGAAAT | 57690 |
rs547134689 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044818 | AGAAATTGTTTGCCA[-/C]CCTGGTTGGTCTAAG | 57690 |
rs547155124 | snp | C/G | 0.000287801 | 0.0119924 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050988 | GAACAGTGGCTGGGG[C/G]AACAGCACAAATACA | 57690 |
rs547166820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042750 | TAGTGGTCATCATGA[C/T]GCTGGTGGTGATCAT | 57690 |
rs547188474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036930 | TTCCATTAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57690 |
rs547253424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017873 | GCGCACACATACACA[C/G]AGACATACTCTACCT | 57690 |
rs547274456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057140 | CACATGCTGAAAGTA[G/T]GTTAAGTTTAGTATA | 57690 |
rs547289890 | snp | A/C/T | 8.29145e-05 | 0.00643826 | missense | TNRC6C | GRCh38.p7 | 17:78049495 | CAGAACGGGAACCCA[A/C/T]CAGGCACTTTAGGTG | 57690 |
rs547299870 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051998 | TAAGGTGGCAAAGTC[A/G]TGAGCATGTTTCAGA | 57690 |
rs547307474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103112 | CCCAGGTGCCTTTTG[C/T]AAACCAGAGGCTCTG | 57690 |
rs547357326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030719 | CCTAAAGATTCCTTC[A/G]TTTTATAAATATTGA | 57690 |
rs547452999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084225 | GAAGGCGGAGGTTGC[A/G]GTGAGCCTCGCACCT | 57690 |
rs547462455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043786 | AATTATGTTCGTTTT[C/T]AACTCCCACAAATAA | 57690 |
rs547610401 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003842 | GCCAGGGCAGGAGAT[C/T]GCTTGAGCCCAGGTA | 57690 |
rs547751892 | snp | C/T | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78071164 | CAGACATGGGCTTCC[C/T]GGTAACTGGCGTCGT | 57690 |
rs547793089 | snp | C/G | 0 | 0 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031532 | GCCAGAACCTACTAA[C/G]ACCTGTTCAAGCCAG | 57690 |
rs547808797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098267 | TAGAGAGCACTCTGT[A/G]TGGCTCCCCAAACAC | 57690 |
rs547813110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078354 | TCACCTATTTGTCAG[A/G]TAACTCATTACACAG | 57690 |
rs547843656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004440 | AATACAGGTGACAGC[C/T]GTAAATGTCTAACTT | 57690 |
rs547871887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005625 | TGGAGATTCAGAATG[A/G]ACAAACTGAAAGCCA | 57690 |
rs547876567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090834 | GACTCTTTCAGAGCA[A/G]ACTTTTGTAAAGGAA | 57690 |
rs547881351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066625 | CTTTGCCCTTCTTCA[C/T]ATTCTTCCAAGAAGT | 57690 |
rs547905126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012032 | CTAAATTGGCCTCTA[A/G]AGTTGGGCAGAAAGA | 57690 |
rs547915619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097292 | CCCAGTCAGAAGAAA[C/T]ACTCAAATTTTTATG | 57690 |
rs547959316 | snp | C/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086746 | AGGAGGTTGGCCTAG[C/G]CAGTAGTGGCCTCAG | 57690 |
rs547978171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058900 | TAGTTTTCTGAAACA[A/G]TTATCATCTTATAAA | 57690 |
rs547994463 | snp | C/T | 0.000798403 | 0.0199641 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104767 | CCCGCCCAGCGCCGA[C/T]GACAGCAGGGTGATA | 57690 |
rs547999076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032116 | TACATTGGTCCATAC[A/G]AACCCATCAAGGCAG | 57690 |
rs548033338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033502 | TGGAGAAACCCAGTC[C/T]GTACTAAAAATACAA | 57690 |
rs548043858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085980 | TTTTTTTAGTTCTGC[A/G]CACTAAAAAAGTGGA | 57690 |
rs548071838 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107081 | CGATGGACATACACC[A/T]GCGTATGTATATCCA | 57690 |
rs548113430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095688 | TAGGGATACATTAGG[A/G]TTTGTTATTGAAAGA | 57690 |
rs548133579 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053094 | ACCATGTCACGTTGC[A/C]CCCCGACCCCTGACG | 57690 |
rs548136110 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037825 | ACTAATTCCAAACTT[C/T]ATCTAGAAGAGCGAA | 57690 |
rs548169468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059571 | TACAGTGTGAGGCCG[C/G]ACACAGTGGCTCACG | 57690 |
rs548171918 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021569 | AATAGGTTATTTATT[A/T]TTTTATTTTTATTTT | 57690 |
rs548198092 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105407 | TATGCACATTACCCT[C/T]GTTTCATTACTTTTT | 57690 |
rs548205301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013686 | ACAAAGGAGCCCAAA[C/T]TTGGCAGGAGTTGTG | 57690 |
rs548240018 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106433 | TTGCACATGCCGGAC[A/G]CGCTCTCAGGAAAGC | 57690 |
rs548305128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074484 | TGCAAACTGCCAGGG[C/T]GGGACAGAGCAGCGT | 57690 |
rs548356691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039796 | CAACAAGCCCGAGAG[A/G]AGGAGGGCCTGTGGG | 57690 |
rs548386703 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042727 | GATGGTGGAGATAAC[-/AAT]GATGGTAGTGGTCAT | 57690 |
rs548444660 | snp | A/C/G | 0.00398691 | 0.0444912 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039316 | CAAATCTTGCCCCCC[A/C/G]CCCCCACTCCCTACC | 57690 |
rs548476317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022061 | ATGCCCAGAGGCAGT[A/G]AGACTCTCACCAAGG | 57690 |
rs548478155 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014379 | ATTACAGGAGAGCCA[A/G]TAGGCATTAATGCTG | 57690 |
rs548480906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045696 | AAAAGATATTTGCCA[C/T]GCCCTCAAGGAACTC | 57690 |
rs548499272 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006442 | ACTATTGTCATTTCA[A/C]AATACAGAGTTAACT | 57690 |
rs548529763 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035604 | GAGCCCAGGAATTCA[A/T]GACCAGCATGGACAA | 57690 |
rs548584434 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081654 | CAGGAACAGGGGAAA[A/G]GGCAGCACTACTGTG | 57690 |
rs548592627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028038 | GTAGCTGGGACTGCA[A/G]GCGCCCGCCACCATG | 57690 |
rs548617093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074024 | ACCATATCATTGATT[C/G]ATGATCATTGAACTC | 57690 |
rs548617601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067551 | ACAAATAGCTGATGT[A/T]TGAAGGAAAAATTAT | 57690 |
rs548621491 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107134 | GTGTGCGTATGTGCG[C/T]CCGACATACCACTTC | 57690 |
rs548653215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040827 | CTGTAAAATCCCATC[C/T]GTCCATGCCTCCGCC | 57690 |
rs548681055 | in-del | -/TT | 0.999999 | 2.25845e-05 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108305 | TCTGACCATACTCTT[-/TT]GGAAATTGAGAAGGA | 57690 |
rs548724061 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069486 | ACTCCTGGGCTCGAA[C/T]TGTCCTCCTGCCTCA | 57690 |
rs548776995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054375 | CACTGCAGACTACTG[C/T]ACACTACTGGAGACT | 57690 |
rs548789088 | snp | A/G | 1.65908e-05 | 0.00288012 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093669 | GAATATTGACCCTGA[A/G]AATGACCCTGACGTC | 57690 |
rs548789517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100712 | TAACATGCAGCTCCT[C/T]GTTACTTAGGCAAAT | 57690 |
rs548789952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048512 | CAGTCTCTGTATTTA[C/T]AGGAGTTGCAAAGTC | 57690 |
rs548819615 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027675 | GCCTCTCTGACCCCA[C/T]TGATTGTGAGACATA | 57690 |
rs548879226 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107518 | CTACTTTGCACGCTG[A/C]GATTGGGAGAGCTGT | 57690 |
rs548880986 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024833 | AGAGTCTTGCTCTGT[A/T]GCCCAGGCTGGAGTG | 57690 |
rs548898209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023962 | TAAAAATACAAAAAT[G/T]AGCCAGGCATGGTGG | 57690 |
rs548924764 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005587 | GCATTTCTCACTGTT[A/G]CTCAGGAACTCCTAT | 57690 |
rs548925449 | snp | G/T | 3.49473e-05 | 0.00418 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067948 | ACACTCTTAACGACG[G/T]TACACCCTGAAAACC | 57690 |
rs548935375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060427 | AAGCACATAGCAAGC[A/G]CTCAATAAATGCCTG | 57690 |
rs548936679 | snp | A/C/G | 0.00122729 | 0.0247417 | missense | TNRC6C | GRCh38.p7 | 17:78067843 | GATGAAGAAGGGGAC[A/C/G]TGTGGAATAATGCTG | 57690 |
rs548957708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075632 | AAATTACGTGTTAGA[A/T]GTTTATCCTCAGGAA | 57690 |
rs549002105 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030327 | CTTGTGTGTGTGCGT[-/GT]GTGTGTGTGTGTGTG | 57690 |
rs549022568 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066867 | CTGACTGTCACGAGT[A/G]GACAGGTTTGAGAAG | 57690 |
rs549047267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082266 | CTAAGTTTAGTGAGG[A/G]CAGGGGTAGGTTAGT | 57690 |
rs549081839 | snp | C/G | 1.80899e-05 | 0.00300743 | missense | TNRC6C | GRCh38.p7 | 17:78050305 | AGCACTGGGAGGGAA[C/G]GAACGGGAGAAGGCC | 57690 |
rs549097971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096045 | GACAGAGCAAGACTT[C/T]GTCTCAAAAAAAGAA | 57690 |
rs549099796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062808 | CAGTTTGGGATTAGG[G/T]TTACCAAAAGTATAA | 57690 |
rs549107708 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031024 | AGATCACTTGAATCC[A/G]GGAGGTGGAGGTTGC | 57690 |
rs549118487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056007 | CTCTCCCCTTTGATA[C/T]GTGATCCTTAGAAAC | 57690 |
rs549159215 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107093 | ACCTGCGTATGTATA[G/T]CCAATATGTGTGCGT | 57690 |
rs549192614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023272 | CCAGTCCCTCTTGGA[C/T]ACTGAAGGATGACTG | 57690 |
rs549278787 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009828 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 57690 |
rs549353918 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002312 | ATTCTTCTCAGGGCC[A/G]CAGAGAAAGAGTCCT | 57690 |
rs549361235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017952 | CAAAGGAGCTTTCTG[A/T]ATCCCTAAATTAGGT | 57690 |
rs549370238 | snp | C/T | 1.65652e-05 | 0.0028779 | missense | TNRC6C | GRCh38.p7 | 17:78049553 | GCACAGAACCACAAA[C/T]GTCCACTTCTCAGAA | 57690 |
rs549443112 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003068 | TTCAGCAGTGGTGCA[A/G]TTCTGGGTGGTTAGG | 57690 |
rs549455685 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010258 | TATTAAACTTTACCA[C/T]GCGTTCAGTTTGTAA | 57690 |
rs549466188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016836 | GTAGATTAGCAATCA[A/G]TCCTCAAGGAACTCT | 57690 |
rs549503985 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016392 | CAGCTCTCCTTGCAC[A/G]GAGGCTGCATAAGCT | 57690 |
rs549534465 | in-del | -/ATTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063318 | GAAAGTACACTTACT[-/ATTC]ATTAGGTGGAATTGG | 57690 |
rs549536013 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076360 | CAGGGTGAGGCTCAC[A/G]TCTTCATCCTGCCCC | 57690 |
rs549543243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025176 | TTTGACATGCACAGT[A/G]TTGTGTATCTGTCAT | 57690 |
rs549645952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043721 | CTTCTCCACTTCTCC[C/T]CACCCCTCACTCTCG | 57690 |
rs549651466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076962 | AGTAGCAGCTAATAT[A/G]TGTGTTTGTAAAATA | 57690 |
rs549675335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103921 | GACCCCATCTCCAAA[C/T]GTAGTCACATGGGGA | 57690 |
rs549681792 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011653 | TTAACATTTATGTAC[A/G]AGTCTTATATGGCTA | 57690 |
rs549684656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042842 | ACAGTGGTGATGGTG[A/G]TGGTGGTGATGATGA | 57690 |
rs549702699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004660 | TCTTTTACGAATCCT[A/G]TTAGTAAAGATTAAA | 57690 |
rs549717062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051675 | ATATATTAAGCACAC[G/T]CAGTAGAACATCAAG | 57690 |
rs549722442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032287 | CATACACATTGAGCC[A/G]AGCCTATCTGATACC | 57690 |
rs549765742 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071916 | ATTCATAATTGTAGG[G/T]CGTTCCCCTGAAAAT | 57690 |
rs549822775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064199 | TTCCCGGGTTCAAGA[G/T]ATTCTCCTGCCTCAG | 57690 |
rs549985568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091043 | CATGTTTATTCAGCA[C/T]TGAAACAAGTAAAAT | 57690 |
rs550018811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066343 | TTTTGTACTTTGTGG[G/T]TTTTTTTGGTTTTTT | 57690 |
rs550080319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033408 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 57690 |
rs550130714 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048740 | GTGTTTGTCATTCAG[A/G]TTTGAAGACTTGAAA | 57690 |
rs550134191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057317 | TCTTTTGCAGTGAGA[A/G]CAAAGTTCATCACCC | 57690 |
rs550163125 | in-del | -/GACCCCTCCCGG | 0.000399281 | 0.0141238 | cds-indel | TNRC6C | GRCh38.p7 | 17:78104875 | AGCACCAGGAGAGCC[-/GACCCCTCCCGG]GACCCCTCCCGGCTG | 57690 |
rs550167570 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075873 | ATGCAAATGTCGAGC[C/T]TTGAAAATAAAATTG | 57690 |
rs550170129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053608 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAAACTCT | 57690 |
rs550183551 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098899 | TCTCTGCCCCCATGA[C/T]TCCCCTTCGCACAGG | 57690 |
rs550228722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026710 | AGCGTTACAAGACCT[C/T]AGAGTTTTAAACCAG | 57690 |
rs550235998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044966 | CCAGGCAGGGGATGG[C/T]ACCTTTAACAGCCCT | 57690 |
rs550249462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072867 | TACATTTTCTTATTA[C/T]AAGTATTTTTAATTC | 57690 |
rs550255881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053147 | ATCAGTAGCCACTGA[A/G]CATCATCAAGCTTGC | 57690 |
rs550285924 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107205 | TTTTAAAATTGGGGA[G/T]GGAAGTCAAGAATAT | 57690 |
rs550314321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045776 | AGACTGCTCTGCCGC[C/T]TGATTTGTATCACAT | 57690 |
rs550334098 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089705 | GTGATTCTTACAGGG[-/AT]CTCTAGAGAAGGAAA | 57690 |
rs550345410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020452 | GCTTGTGATCTGTCA[C/G]AACTTGTAGTTTCTC | 57690 |
rs550373789 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078173 | GCGATCTGACATTGC[C/T]CCCTTGGTGGTGGTG | 57690 |
rs550380913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081144 | TCATGTGGTGGAAGG[A/G]GCAAACAGGCTTCCT | 57690 |
rs550384128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027403 | TCCCTGGGCCCGTTA[A/G]AGGTTGGAAATGCAA | 57690 |
rs550385731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024280 | TTGTGAAAGAGACAG[C/T]AAGTTTTCTTCTCTG | 57690 |
rs550406500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073424 | CTGAGTGCGTTCCTC[A/G]TGCCTTGCCCCAGAA | 57690 |
rs550416339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098972 | TCACTGGGACGTAAG[A/G]CTTTTGCAGGCCCAA | 57690 |
rs550419634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080395 | AGATTGCGGTGAGCC[A/G]AGATCACACCATTGC | 57690 |
rs550419705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087374 | CCTCCCACCTCAGCC[A/T]CTTAAAGTGCTGGGT | 57690 |
rs550507669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086788 | TGAAGAATGCATTTG[C/G]TCCCTAGACAAGCCA | 57690 |
rs550519675 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046398 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 57690 |
rs550520735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074160 | CCTCAGCACCACACA[A/G]GGGGACCATTTTAAA | 57690 |
rs550545495 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100736 | GGCAAATTTCTGCAC[C/T]CAGCTTGAATTTTTC | 57690 |
rs550547050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040759 | TGACAATCGAAAGAA[C/T]TTAAAGAGGAAGGAA | 57690 |
rs550556748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100901 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 57690 |
rs550559169 | snp | C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108252 | CCCGCCACAGGCTGG[C/G]CCCCCCCCACCCATG | 57690 |
rs550593909 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107579 | TCAGAGCTCACATAC[A/G]TACCTCTCTCACGAG | 57690 |
rs550665030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014187 | AGATTTAGGATTTGC[C/T]ATTTGTTCTGAGAGC | 57690 |
rs550690147 | in-del | -/T | 0.252702 | 0.249985 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027904 | ACAGAAACTTGGAGG[-/T]TTTTTTTTTTTTTTT | 57690 |
rs550695764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023042 | TATTGTCCCAGCTAT[C/T]TGGGAGGCTGAGGTG | 57690 |
rs550707299 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106273 | AAAAAAAAAGACTTC[C/T]GTCGTAAAGAAACCT | 57690 |
rs550711533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013768 | CACTCCTACATAGAG[A/G]GGGAACAGCATCTGT | 57690 |
rs550721020 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040975 | CTTCCTGGCAGCTCC[C/G]TGGCAGCTCTACAGG | 57690 |
rs550756501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034691 | GAAAATGTTTGAGGT[C/T]GGGCGTGGTGGCTGA | 57690 |
rs550758954 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055284 | AGCCTAGGCCTACAC[A/G]GGGCCGGGATCTTCA | 57690 |
rs550776258 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034198 | GAGTAGCTGGGATTA[C/T]AGGCGACCACCACCA | 57690 |
rs550808568 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069655 | AACAATAATTTATGT[A/G]TACATTGATGGAGTA | 57690 |
rs550816347 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009353 | TTTCTGGGTGTTTTC[A/C]TGGATTGAGTGAGGG | 57690 |
rs550834023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039828 | ATTTCAGCTGTCAAA[C/G]GGCTGTCCTGAGAGC | 57690 |
rs550847049 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104089 | ACACAGGGCCCAGCA[C/G]TGGTCCTCACAGCCA | 57690 |
rs550865356 | snp | A/G | 1.66161e-05 | 0.00288232 | missense | TNRC6C | GRCh38.p7 | 17:78049438 | GGCAACCCTTCCAGT[A/G]TTTGCAGTCCAGTCA | 57690 |
rs550921064 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029570 | GTGGTGAGTGAATGT[G/T]AAGGCCTAGGACATG | 57690 |
rs550950298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014916 | TCAGAGCTGTCTTCT[G/T]CTCGCATCTCATTGT | 57690 |
rs551000855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061155 | AAGACCCCATAGTAC[A/G]GAAATATTCTGCAAA | 57690 |
rs551010538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036298 | GGAAGGAATTGACGG[A/T]GTTTGAGTCACCTTT | 57690 |
rs551045736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035806 | GGTGAAATTCTATTG[G/T]TGTATTCCCGAGGAG | 57690 |
rs551048317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068030 | CCTGAGGTTCTCAAA[A/G]TAGTCTTAGGACCCT | 57690 |
rs551086508 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097957 | TATTGGCTCTTTACT[C/T]ACTCCCTGAGCTGGG | 57690 |
rs551090300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78002187 | CTACTTGATCATATC[A/G]GAAAATAAAGTTTTC | 57690 |
rs551114429 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044448 | GAGCCAGAATAGGTA[C/T]GCCTTGCCTTCATGG | 57690 |
rs551126098 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041497 | GTTTTGAAGAAAAAC[A/T]CAAGGCAACAAACTT | 57690 |
rs551129430 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056114 | TTTGGCCTCCCAAAG[G/T]GTTGGGATCATAGGT | 57690 |
rs551136370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088085 | GTAGTGAATTTGCTG[C/T]CAGCAGATAATATTC | 57690 |
rs551162901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048606 | TTGTGAGTATTCTCC[A/G]GGGGGAATAATAGTA | 57690 |
rs551173047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042150 | ACTTAAGACAGTTAC[A/G]TTGCTTAGATTTTTA | 57690 |
rs551202615 | in-del | -/C | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024884 | CTGCAGCCTCTGCCT[-/C]CCAGGTTCAAGCAAC | 57690 |
rs551231351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094469 | TTTGAGACAGATTCT[C/T]GCTCTCTTGCCCAGG | 57690 |
rs551284268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016873 | AAGGGATTCTTAGCT[C/T]CCTTTTATCCCCCCG | 57690 |
rs551321057 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024529 | CTGCCACCACGCCCG[A/G]CTAATTTTTTGTATT | 57690 |
rs551326778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061704 | TAAATAAATATCAAA[A/G]TGGAAATATTTGGTT | 57690 |
rs551351315 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026425 | ACATTATCAATTGCA[C/T]TATGCACTATTTTAT | 57690 |
rs551382129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070534 | TCTGTAGCTGACCTT[C/T]TTCCTCATCCTCTCC | 57690 |
rs551403771 | snp | C/G | 1.65941e-05 | 0.00288041 | missense | TNRC6C | GRCh38.p7 | 17:78050945 | GTAATAGGTCAGGGT[C/G]TGGTTGGAATGACAC | 57690 |
rs551418291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082750 | TGGGATAGGAATCTT[A/G]GTGATGTGAAACCTC | 57690 |
rs551418389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075706 | GCCCTTGTCAGTTGG[C/T]CACATGAGTGACCAC | 57690 |
rs551439134 | snp | C/T | | | missense | TNRC6C | GRCh38.p7 | 17:78049505 | ACCCAACAGGCACTT[C/T]AGGTGCTTGGGGAAA | 57690 |
rs551453199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082328 | AGATGATCACATGGG[A/G]ATGAAGTAATTCTTT | 57690 |
rs551472196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090110 | ATGGGCTTGCAAAGG[C/T]GTTTTGTTAGGTCTG | 57690 |
rs551510582 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104983 | AAGACGAACCTTGGC[C/T]GCAGTCCTTGCGAAC | 57690 |
rs551521918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064040 | AGTTAGAAAATGGCA[A/G]TTTTTTATTTTTTCA | 57690 |
rs551546608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081872 | TGTTACCTGTGAGTA[C/G]TGATAGGAAGGACAC | 57690 |
rs551559481 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020274 | TGTGAGAACAAGTAC[A/G]TGGGTAAACTGAGTG | 57690 |
rs551589085 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014452 | CTAAATTGATCTTCT[A/C]AATAAGCCTGTTGTT | 57690 |
rs551597143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102605 | TTCCCGCTTGGCCCC[C/T]AATGCAGATGAGGCT | 57690 |
rs551618924 | snp | G/T | 3.35329e-05 | 0.00409455 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077189 | TCTCCAATCAGGATG[G/T]CGGCCTCGTGGAAGA | 57690 |
rs551636536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109313 | ACAGTGGGGCATCCC[A/G]AGAAGATCCTCTGCA | 57690 |
rs551688096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069816 | ACCCTATTTTGTGGG[A/G]TAGGAGGAAGAAAAC | 57690 |
rs551706250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083772 | AGAATGGCTGATGTG[A/T]CCTAATAATTCTTGA | 57690 |
rs551718609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108997 | CCACAGGCATGCATG[C/T]GCCACCCCACCCAGC | 57690 |
rs551732533 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076311 | GAGAGTCCTCCAGCA[A/C]GTGATCTGCCTCAGC | 57690 |
rs551788281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103980 | GAATTGGGGAAAGGC[A/G]ACACAGGTCAGTTCC | 57690 |
rs551789873 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003757 | ATTTCAGAACCCTAG[A/T]GATCAAGTGGAAAAA | 57690 |
rs551803575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037724 | AGTAATAGTAATAAA[C/T]CAGCATAAAAGCTTC | 57690 |
rs551827638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089613 | GTTATTCTCAGTCTT[A/T]TGCCACCTGGAGTTC | 57690 |
rs551851526 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003198 | CTACCTAATATCCCT[A/G]AAGCAAAACCCACTG | 57690 |
rs551851592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011543 | GCTGAGCAGTGTTCC[A/G]TTGTGTAGGTGTATC | 57690 |
rs551851779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072489 | AGGAATCCTGTCCTA[A/G]GAGAGCATCCTGTCC | 57690 |
rs551913051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102996 | TAACATTTTTTAAAA[A/G]AGTCGTTTGGCCACA | 57690 |
rs551919317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010945 | GGAAGTGAGCCTAGC[A/G]GCAAGGAAGCGGGGC | 57690 |
rs551943422 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006291 | AAAAAGCAGCATAGC[A/C]AAAAGGACATTTTTC | 57690 |
rs551952957 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061922 | TTGACTTAATTAAAT[A/G]ATTTGTAATACCTAT | 57690 |
rs552031470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030841 | TGGTGGCTCACACCC[A/G]TAATCCCAGCACTTT | 57690 |
rs552034887 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044327 | TCATTTATATTACTA[G/T]CAAACTGCTTTCAAG | 57690 |
rs552038270 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038658 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 57690 |
rs552096458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090692 | GGACAAATAACCAGG[C/T]ACCTGCTTTTAGCTA | 57690 |
rs552130311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045099 | GGTGACCCACTGGGC[A/C]TTCATTTGGAAAAGA | 57690 |
rs552141184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027477 | TATATTCAGTTCCAT[C/T]ATATGGAAACTCTGG | 57690 |
rs552155688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065968 | GGGCATGGTAGCTCA[C/T]GCCTGTAATCTCAGC | 57690 |
rs552158749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091658 | TGCTGGCTTATTAAT[C/T]GATCGTCCTGTTGTA | 57690 |
rs552232468 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107804 | TGGAGTCCTGGCAGA[C/G]GAGTGCCACTCACTT | 57690 |
rs552240038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026618 | CTTGCTGAACCTCAA[A/C]GCTAAGTCTGGGGAA | 57690 |
rs552320767 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053783 | CCACCTGTAATCCCA[C/G/T]CTACTTGGGAGGCTG | 57690 |
rs552325498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025857 | AGGGAAGAGGAAATC[C/T]GTGGACTCTGGAATG | 57690 |
rs552444165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053001 | CCTTTGGAAACCTGA[A/G]AAGTCTGACATTGGA | 57690 |
rs552454128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028006 | GTTCACGCCATTCTC[C/G]TGCCTCAGCCTCCCG | 57690 |
rs552461731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060835 | AGCTATAATTAATTT[A/C]TTATTTCATAGAGGA | 57690 |
rs552481793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052406 | TAGGCTGTACTCTAG[C/T]AGCTGGGGAAACTGC | 57690 |
rs552490653 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107414 | GCTTTCGAAAGTACA[A/G]CGCTTTATTGAATCT | 57690 |
rs552519095 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019354 | AAAATCAAGTTCTCC[A/G]AAGTCTGAAGGGACA | 57690 |
rs552561140 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107701 | ACAGCCAAGCTTTCC[A/G]GCTCTCCACCCCCGT | 57690 |
rs552569643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033445 | GAAGCCAAGGTGGGC[A/G]GATCACCTGAGGTCG | 57690 |
rs552627460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073545 | AACCCTAGTTCTAGA[C/G]CTGCTTTAATAATAA | 57690 |
rs552635405 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097560 | CTCCCTGAGTGGGTA[-/C]AGGGACCCAGAGTAG | 57690 |
rs552645383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034109 | CCCAGGCTGAAATGC[A/G]ATGGCACAGTTTTGG | 57690 |
rs552654693 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039209 | TCCAGTGACCAGCAA[C/T]CTCACTTTATCCTGT | 57690 |
rs552666202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079698 | CTATAAATTAATTTT[A/C]GACTATAAAGTAGTA | 57690 |
rs552680138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080580 | GCACATTTTACAATT[G/T]TAGGCTTTGGACCAA | 57690 |
rs552687445 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085843 | TAGGTTGGTTTTTTG[G/T]TTTTTTTTTTTAAGT | 57690 |
rs552713749 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014213 | AGAGCTCATTTAGTT[C/G]AGGATGATTTAGCAT | 57690 |
rs552737322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040019 | GGCTTCTGCAAGACA[C/G]GTAGGCCAGGGTGCC | 57690 |
rs552765902 | snp | A/C/G | 0.000234231 | 0.0108196 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086936 | GCTCGTGAAGCAGCC[A/C/G]CCACCGCCACCGCCC | 57690 |
rs552773188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068235 | CTTAAGCCAGACATA[C/G]AGATTTGCCAAAAGG | 57690 |
rs552799477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099917 | ACAGGCATTGGGTAA[A/G]TACAGTCATTCCAAA | 57690 |
rs552835421 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087593 | CTAGTCTACTCTGAA[C/G]TGTACTTTACCAGCC | 57690 |
rs552845902 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107624 | CCATTGTTTTGCTTT[A/C]TTCTATCATTTGCTT | 57690 |
rs552875310 | in-del | -/TGTT | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044375 | CATTCATTCAATGTA[-/TGTT]TATTTACTGCTTCTT | 57690 |
rs552895106 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052640 | TTTTTGGTTTTTGTC[A/C]TAAGCGTTCAACAGG | 57690 |
rs552898430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074208 | AAAGCACAGAAATAC[A/G]AAAAGCCTGGCAATA | 57690 |
rs552930250 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078832 | TCGGGGTGGCTCACA[C/G]CTGTAATCCCACCAC | 57690 |
rs552940083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073947 | CTCTGTCACATGCCC[A/G]GATGTTACTTGAGTA | 57690 |
rs552941251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094521 | TTGGCTCACTGCAAC[C/T]TCCGCCTCGCAGGCT | 57690 |
rs552958887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027688 | CATTGATTGTGAGAC[A/G]TATCGGTATTGCACA | 57690 |
rs552979935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093999 | TTTTTTTTTTTTTTG[C/T]GATGAAGTCTCACTC | 57690 |
rs553008231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039329 | CCCCCCCCACTCCCT[A/G]CCTCTTACCAGGTCA | 57690 |
rs553011744 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032592 | TCGGTTTCAAGTAAC[A/C]ACTAATAATTGGTGC | 57690 |
rs553122740 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014428 | AACATATGCTCTTAG[C/G]GGCATTTTCTAAATT | 57690 |
rs553152485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008507 | TATTCAGCCCCGGGG[A/G]TTTTCACTCAAATAG | 57690 |
rs553173858 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106815 | GCTCCCTGCCTGCTT[C/G]ATCAGGAAACTTGTG | 57690 |
rs553180718 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054495 | CACTGCAGACTACTG[A/T]ACACCACTGCAAAGT | 57690 |
rs553193377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015041 | GGCACAAGAGAATAG[C/T]TCTCTTACATAGTCA | 57690 |
rs553194311 | snp | A/G | 0.00101158 | 0.022467 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067734 | ACATGAATTTGATAA[A/G]TTCATGTTTGCTCTG | 57690 |
rs553252496 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008304 | TAAAATTACCACTGA[A/G]CAGAAATTTTGTTCC | 57690 |
rs553296354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040993 | GCAGCTCTACAGGAG[A/G]CGGCTCTCGCTGTAC | 57690 |
rs553298621 | snp | A/C | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011121 | TCTAAAGGATGCTGA[A/C]AGTCTGCTGTCTAAA | 57690 |
rs553318202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028099 | GAGACAGGGTTTCAC[C/T]GTGTTAGTCAGGATG | 57690 |
rs553319176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087749 | TGTGATTTGTATAAT[C/T]GACCAAATCAACATA | 57690 |
rs553383937 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046867 | GTCATATAATTGAGT[A/G]TGAACCTGTCAAATT | 57690 |
rs553392119 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088182 | CTTGACATATTATAA[A/T]TGTGGTATATCTTTA | 57690 |
rs553453972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007613 | TGTGTGTCTATGAGG[G/T]CAGGGGCCACATTTG | 57690 |
rs553498675 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063269 | ATATATATATAAATA[-/AT]ATATATATATATGTA | 57690 |
rs553513349 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085703 | CTCTTAGCTTTCATT[C/G]CCATGATGTTAGGGA | 57690 |
rs553515860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043276 | GAAGATGTACCAGGC[C/T]ACAGTGTGGCCCCGA | 57690 |
rs553578631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030018 | TTGTTTTTGGCTTTT[C/T]TTTATGTAGAAGCAA | 57690 |
rs553629916 | in-del | -/ATCA | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010425 | CATATAAAGTTTAAT[-/ATCA]ATCAGAATGAAAAGT | 57690 |
rs553668876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074288 | ACCTGAACTGGGAAC[C/T]TGGGCAACTCACATT | 57690 |
rs553678846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041670 | CCTGAGATCTTTACA[C/T]CCAGTAAATGCAGTA | 57690 |
rs553728584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070796 | GATAGTAAAAGTAGT[C/T]TATATTTGTGATAAA | 57690 |
rs553742299 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002621 | GTTCAGGCTGGGTGT[C/G]GTGGCCCACACCTGT | 57690 |
rs553802082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010432 | AGTTTAATATCAATC[A/G]GAATGAAAAGTAGTA | 57690 |
rs553849828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029758 | CTTATTCTGTAAGCT[C/T]TTTTCTGTGTTTAAT | 57690 |
rs553852666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069937 | ATAAGAAACTGCTAT[A/G]AGTAGTGCCTCTTCG | 57690 |
rs553862911 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093796 | CCTGCCTCTGCATGG[A/T]CGGTCTCTCTAGACC | 57690 |
rs553896997 | snp | C/G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059229 | ATAGATCCCATTGAC[C/G/T]TCTGCAGCCAGAAGT | 57690 |
rs553930464 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003299 | TTACTACAGAGTTGA[G/T]GAAAGGCTTTCAGAT | 57690 |
rs553939860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076634 | AATAATGCACAGGCT[C/G]GTTGTGATGTTAGAT | 57690 |
rs553948264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075779 | GGTCACAGCTCAGCC[C/G]CCAGTGTTGTCATGT | 57690 |
rs553954038 | snp | A/G | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037280 | CCTTTCAGAACGGTG[A/G]TTTTGTCATGTGTGT | 57690 |
rs553956076 | in-del | -/TC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088625 | TTTTTCTTTTTTTTT[-/TC]TCTCTCTTTTTTTTT | 57690 |
rs553994413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010971 | GGGGCGCTGTGCTCC[A/G]GGGGCGCCTCCCGAG | 57690 |
rs553997551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089716 | CAGGGCTCTAGAGAA[C/G]GAAAAGTTCACTTTC | 57690 |
rs554004387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064584 | ATGTAATACATTTGC[A/C]TCCTTTAAATTTTCT | 57690 |
rs554040385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096183 | AACAGACAGCTCACA[C/T]GTTCCCACTTACAAA | 57690 |
rs554040446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089264 | TGAGCCACCGTGCCC[A/G]ACCACTTATCTTTAC | 57690 |
rs554051868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102646 | GCAGGATAGTTGGGG[G/T]TTCTTGGTCAGGGTC | 57690 |
rs554054511 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011800 | GTTTCACAGTTCTGC[A/G]TCTTCACCAATGTGT | 57690 |
rs554089780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067309 | TGTGATTGCACTACT[A/G]TAATCCGGGCAACAG | 57690 |
rs554090291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030916 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 57690 |
rs554142065 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088289 | GAAGTAGGTAAGACC[G/T]GACTTAGGAATTAGA | 57690 |
rs554173884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091268 | GAGGCGGAGGTTGCA[A/G]TGAGCCAAGATTGTG | 57690 |
rs554201079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083838 | TAATTTTCAATCAGT[A/C]TTACTGATTTTACTA | 57690 |
rs554261319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084524 | TGTCCCAGAGACACA[A/T]GCTATGTGTCCTCGC | 57690 |
rs554303513 | in-del | -/AGT | 0.00263152 | 0.0361779 | cds-indel | TNRC6C | GRCh38.p7 | 17:78049057 | TGTGGCTCAGAGAAC[-/AGT]AGCATGGCTACAGGG | 57690 |
rs554314795 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066824 | TGTCGGGCCCAACCT[C/G]AGGCCTGCCAGACTT | 57690 |
rs554350170 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007835 | AACTAGACCAAATCA[A/G]TTAGAAATTCCCTTA | 57690 |
rs554426804 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092737 | GAAGTTGTCTCAAAA[-/AAAT]AAATAAATAAATAAA | 57690 |
rs554525373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013902 | ATTGGTTCACTATGC[A/G]AGGCATCAAAGAGGA | 57690 |
rs554526824 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058616 | TACTGTGTCTTCCAA[C/G]AATGGCTAGAAGTAA | 57690 |
rs554571740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078823 | CACAAAAATTCGGGG[C/T]GGCTCACACCTGTAA | 57690 |
rs554575697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038457 | GGCAGGTGGATCACG[A/G]GTTCAGGAGATTGAG | 57690 |
rs554586869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013313 | TGCAGAATTGAAGAC[A/G]AATTAAACAGAGGAG | 57690 |
rs554616288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044635 | TGAGTTGGCAAGCTC[G/T]GGGCCCATGAGCCAC | 57690 |
rs554646523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051850 | TTGGCAGATGACTGT[G/T]TCAGTTCACTGACAT | 57690 |
rs554678357 | snp | A/G | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108041 | CCTAGGACACTGGCC[A/G]TGGCCTTCAGGGTGA | 57690 |
rs554687228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058171 | GACCTGCTACCTTGC[A/G]CTCTGCTGTGCATAC | 57690 |
rs554717047 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105278 | CACATGACCAGAGGC[A/G]GCCGGTAATCAGGGC | 57690 |
rs554717310 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040190 | AGCAACAGATCTTAA[C/G]TGGGAAGATGAGTAT | 57690 |
rs554724632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059277 | TATGCAGTAGTTACT[A/G]AAAGAGAAATTATCT | 57690 |
rs554754311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039518 | CCTAGATGCTTTTAA[C/T]ATTCGATAATGCTGA | 57690 |
rs554783268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027601 | TGTGAGTTGAAGACC[C/T]AGGACACGCAAAGTC | 57690 |
rs554784283 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073229 | ACAGTGAAGGGGCAA[C/G]CACACAACAAGCTGG | 57690 |
rs554789897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105015 | GTTCGCAAAACAGTG[C/T]GGGCTGCGGTGGGTC | 57690 |
rs554793932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032456 | GCTTCTTTTCCAATC[C/T]CCTTGACTTGATGGA | 57690 |
rs554816205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079197 | GAGGCTACAGTGAGC[A/C]AAGACCGCGCTACTG | 57690 |
rs554854852 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085026 | GTCCTATTGCTTTCA[C/G]TCCTGCCCGCCGGAG | 57690 |
rs554900467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099332 | ATCAGCTACAGATAG[C/T]GTATTAGTCCATTTT | 57690 |
rs554922717 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007420 | TACTGGTTCAAACCA[A/G]AATTCATTGCCTGAG | 57690 |
rs554957881 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108603 | GCCTGGGAGACCAGG[C/T]TGGATTTTGACAGAC | 57690 |
rs554961667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053853 | CCTGGGCAACATAAC[A/G]AGACCCCATTTCTTT | 57690 |
rs554970495 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059954 | ATCGTGAAATCAAAA[C/G]TGTATAAGATGGTTT | 57690 |
rs554977870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100089 | CATGGTCTTGGGCAG[C/T]TCTGCAGGGTACAGC | 57690 |
rs554986724 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105938 | AAAAGTACAGTGTAT[A/T]TCTCTGGAGAAATAA | 57690 |
rs555013938 | in-del | -/AG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096164 | AATTAACACAGGAAC[-/AG]AGAACAGACAGCTCA | 57690 |
rs555137648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081282 | GGAATTCTCGGGGGA[C/T]GCAGACATTCAGACC | 57690 |
rs555140478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073580 | AAATATTTACATTTA[A/G]ATATAGTCGATTCTT | 57690 |
rs555140904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094125 | GCTGGAATTACAGGC[A/G]TGTGTGCCACCATAC | 57690 |
rs555228470 | snp | C/T | 1.68029e-05 | 0.00289848 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093114 | TGGCTCTAGCATCAA[C/T]TGGCCCCCAGGTAAG | 57690 |
rs555230725 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086404 | AGAAGAGTGGCTAGG[G/T]TCTCTTTTTTTATTT | 57690 |
rs555284106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068416 | CTCATGTCAACAGAA[A/G]TTCTTTGGGATCTTC | 57690 |
rs555296164 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070501 | GGTGCCGAGCCCTCC[C/T]CCACCCCCACTGCTC | 57690 |
rs555333717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082038 | ATACATTTTTTAATG[A/G]CCTTTGACATTTCAC | 57690 |
rs555344904 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020428 | AGGGAAATTCTCCCA[C/T]CTGAAAAAGCTTGTG | 57690 |
rs555359271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021828 | GCCTGCCTCGGCCTC[A/C]CAAAGTGCTGGGATT | 57690 |
rs555385342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028120 | AGTCAGGATGGTCTC[A/G]ATCTGACCTTGTGAT | 57690 |
rs555394569 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064265 | CATACCCAGCTAAAT[A/T]TTTGTATTTTTAGTA | 57690 |
rs555404521 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004073 | CCTGTATACCATATG[C/T]GAAATTCTGACTTAA | 57690 |
rs555409708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074317 | TTTTTTTGCCAATCT[C/G]CACATGTCCACAAAT | 57690 |
rs555422431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034228 | ATGCCTGACTAATTT[C/T]GTATTTTTAGTAGAG | 57690 |
rs555444516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080643 | ATAATATATTTGATA[A/G]TCAATGGTATTGATA | 57690 |
rs555499951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109154 | TGGCAACATCACGGC[A/C]GAACGGTAAAGGCAG | 57690 |
rs555511911 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052917 | TGTGCCTTTTTGGCC[C/T]ACATTTTTTCTGTGA | 57690 |
rs555595731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015773 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCGCCT | 57690 |
rs555613289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054905 | TACCATACACCACTG[C/T]GGACTACTGTATGCT | 57690 |
rs555632742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015260 | TGACATCAGTCATAG[G/T]ACATATCATCTATTC | 57690 |
rs555636892 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108329 | GAGAAGGAAAGCATT[A/G]AGTGGGACCTAATCC | 57690 |
rs555645378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082437 | CAGAGCCTTAAAACA[G/T]AAACACAGTCTGTCC | 57690 |
rs555694214 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083321 | CATGAGTTAGGGAGT[C/T]CTCACTCAAAGGTGT | 57690 |
rs555718163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022292 | TTAGATATAAGATTG[A/G]CTACACATAATGCAT | 57690 |
rs555719526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011039 | CATCTCTGTTTCATA[C/T]AACTTTTCACTAAAA | 57690 |
rs555767330 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035953 | AATGTGGAAGTGACT[C/T]CTACGGTCACTTCTA | 57690 |
rs555773243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042369 | ACTGTTTATTAGTTA[A/C]AAACCCTGGCCACTT | 57690 |
rs555782786 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010647 | AAGGAAATTCCTAAG[A/C]AATTGATTGTATGAG | 57690 |
rs555804130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041744 | AGCATTTATCCTGCC[C/T]CTGAAAACCAAGCAG | 57690 |
rs555860715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016606 | AACCAGAGTAAGATC[A/T]AATCCTCCATTCCTG | 57690 |
rs555913472 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062331 | TTGTTATTAATCATT[A/C]TTACTGCATTTTCTT | 57690 |
rs555916169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009624 | CAGTGGTGCAATCTC[G/T]GCTCACTGGAACCTC | 57690 |
rs555923096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102672 | GGGTCCATAAGTGAC[C/G]CTGCATGGGAGGAGA | 57690 |
rs556029927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075380 | AAAACTTGCTGGACT[A/G]TAATACTTAAGTGAC | 57690 |
rs556078684 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101762 | CCTTAAGGCACAGAT[C/T]GCTCGTGCTACTGTT | 57690 |
rs556098632 | snp | A/C/T | 1.80829e-05 | 0.00300684 | missense | TNRC6C | GRCh38.p7 | 17:78050309 | CTGGGAGGGAAGGAA[A/C/T]GGGAGAAGGCCGAAG | 57690 |
rs556135623 | snp | C/G | | | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077301 | TGGGATTGCCTCCGG[C/G]CTGGGCATGCAAAAC | 57690 |
rs556187346 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031566 | CAACCTGCCGGTACC[A/G]GTACCAGTACTTCCA | 57690 |
rs556214678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056323 | CCACCATGCCTGGCT[A/G]ATTTTTGTATTTTTA | 57690 |
rs556243939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018380 | TGATCCGCCCCGCCT[C/T]GGCCTCCCAAAGTGC | 57690 |
rs556256269 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046977 | TGGAACCAATAATAC[-/T]GTGTATTCGAATGGC | 57690 |
rs556270656 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070430 | AATGCATCATTAGAA[C/G]CTTTGCATTTATAGG | 57690 |
rs556275205 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030912 | GAGACCAGCCTGGCC[A/C]ACATGGTGAAACCCC | 57690 |
rs556331254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043926 | GCTGAACAGTATTCC[A/G]TTGTGTATATCTGCC | 57690 |
rs556338927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063019 | GGGAGGCTGAAGCGG[A/G]GGGATCACTTGAGGT | 57690 |
rs556424117 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087467 | CGTTGTATAGAGCAG[A/G]AGTTTTGCCGCTGCC | 57690 |
rs556469018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083301 | CATGAAGTATTTAAA[C/T]TCTTCATGAGTTAGG | 57690 |
rs556480039 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091341 | CAAAAAAAAAAAAAA[A/T]TTTGCTGTAAGCGAA | 57690 |
rs556480649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100203 | CTGGGGTCTAGAGGA[C/T]GGTGACCTTCTTCTC | 57690 |
rs556483086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065486 | AGTCAAAGCAACCCC[A/G]CATATTATGTTTGAT | 57690 |
rs556505894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089841 | AAATAAAGGGGAAGC[C/T]TCACGTAGCACAGAA | 57690 |
rs556521730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079206 | GTGAGCCAAGACCGC[A/G]CTACTGCACTCCAGT | 57690 |
rs556521796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086191 | AAAAATTAGCTGGGC[C/G]TGGTGGCACACGACT | 57690 |
rs556594366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096361 | TACACCACACCCCCA[C/T]GACGCACAGTTCACC | 57690 |
rs556617747 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067083 | TGTGATGGCTCATGA[C/T]TGTAATCCCAACACT | 57690 |
rs556654115 | in-del | -/TTTTTG | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030156 | TGTGCTAGACTTTTT[-/TTTTTG]TTTTTGGAGACGGAG | 57690 |
rs556696875 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105998 | TTGTGGACTAATGCA[A/G]GAAAATTATTACCAG | 57690 |
rs556705866 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094000 | TTTTTTTTTTTTTGC[A/G]ATGAAGTCTCACTCT | 57690 |
rs556780779 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045528 | CCTCAGAAGATGGAC[A/G]TGCTTGTTCAAAGCA | 57690 |
rs556812790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044767 | AGACTATATGGCCCA[A/C]AAAGCCTAAAGCATT | 57690 |
rs556864919 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073646 | AAACACTGAATTAAC[A/G]AATACCGAACCAGTG | 57690 |
rs556882886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079843 | CCTGCCCAACACACT[C/T]CCATTGATGTGCTTT | 57690 |
rs556915224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007495 | CACAGGTTGGCCTGA[C/T]TGTACCTATGATACA | 57690 |
rs556969369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032579 | ATTCTTCAATTTTTC[A/G]GTTTCAAGTAACAAC | 57690 |
rs557000736 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061635 | CACTATGATCACACT[G/T]AAGAACAGCCACTGC | 57690 |
rs557014492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045205 | ATTTACAGTAATCCA[A/G]TCAAGACATGAGGGT | 57690 |
rs557020946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073295 | TGGAGGTGAATCGCC[A/C]ATGCCATATTTGAAG | 57690 |
rs557030784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091741 | AAAATAACCCATTCC[A/G]TTATAGTGCATATAA | 57690 |
rs557034715 | snp | A/G | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109072 | GCCCAGGCTGATCTC[A/G]AACTGCTGGGAATAC | 57690 |
rs557037772 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014007 | TGCACCAGCCTTGTC[G/T]TACTAAATGTTGGAG | 57690 |
rs557046522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085224 | AGAATCTTTTAGTTA[C/T]ACAGTAAGTTTTTAT | 57690 |
rs557051750 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032064 | TGGCATGAGCTACTT[C/T]AGCTGAGCTTATTTT | 57690 |
rs557052790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052649 | TTTGTCATAAGCGTT[C/T]AACAGGAGAATGTCC | 57690 |
rs557077968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025041 | GGTGATCCACCCACC[A/G]CAGCCTCCCGAAGTG | 57690 |
rs557091088 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056285 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 57690 |
rs557109999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005745 | GTTTAATTTGGGACA[A/G]GTTACTTCACTTCTT | 57690 |
rs557134401 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082684 | GCATCCATTTATAGG[C/T]TCTCCCCAAGGGTCG | 57690 |
rs557139779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066999 | AATACAGAGAAGATT[C/T]GCGTGGTTCCTATGC | 57690 |
rs557172884 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034458 | CACACATGCTTAATT[G/T]CTGCCCCCCCAACCC | 57690 |
rs557194304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099375 | GAAGACATACCCGAG[A/C]CTGGGCAATTTATAA | 57690 |
rs557272301 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029189 | TGGCAGTGCTACAGA[C/T]GCCAAACCACAGTTG | 57690 |
rs557282034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040943 | CGGGTGGCCCGGACG[C/T]AGACTGGCCCCGGGA | 57690 |
rs557290846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046937 | AACAAAGGGCAGATC[A/G]TTTTACAGTGTGACT | 57690 |
rs557318847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093235 | CTAAGGATCTGGAAG[C/T]GTTAAGCCCAGAGCT | 57690 |
rs557348437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061452 | CCTTTAGAGTGTCAG[A/C]TGGTACATCCTAGTG | 57690 |
rs557366564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047907 | GTTGGAAATACTCAA[A/G]TAATTGTTAAAGTCA | 57690 |
rs557416791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028725 | TAAAATATTTTTTAA[A/T]GTTTCTTCTACATAA | 57690 |
rs557431326 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023329 | ATCCAGTGTCAGTTA[C/T]TTACAAAAGAGAAAC | 57690 |
rs557481274 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073653 | GAATTAACGAATACC[A/G]AACCAGTGCTCCTAG | 57690 |
rs557483814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060536 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC | 57690 |
rs557488856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069189 | CAATCCCCTGATACA[C/T]AAAGTCCTAGAAACT | 57690 |
rs557535406 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055423 | TGTGTGCTAGACCTT[G/T]CTGTGACTGGCCGCA | 57690 |
rs557553363 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007089 | CTCAAATGATTCCCC[C/G]CCACCTCGGCCTGCC | 57690 |
rs557557862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053444 | AGACCAGCCTGACCA[A/G]CAAGGTGAAACCCCA | 57690 |
rs557564834 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108869 | TTGTTTGTTAATACA[A/G]GGTCTCTGTCTCCCA | 57690 |
rs557571165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081379 | GTAATTCTCGCTCTG[A/T]AATTGTTCAAACCCA | 57690 |
rs557622404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054996 | ACCATACACCACTGC[A/G]GACTACTGTACACCA | 57690 |
rs557742668 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108416 | ACTTGAACCTGGAAG[C/T]GGCAACCCTCAGCTC | 57690 |
rs557757499 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060511 | GAGTCTTAACTCTGT[C/T]GCCCAGGCTGGAGTG | 57690 |
rs557759856 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009976 | GCAGCCACCACCTCC[A/G]AGGCTCAAGTGATAC | 57690 |
rs557792970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068687 | TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAAG | 57690 |
rs557830779 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107875 | GAAGAGTAATGAGGA[C/T]TTTTTGTGTTTCCTA | 57690 |
rs557843154 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077705 | CCAAAACGACGTTAC[A/G]TCTGTTGATCTGCGA | 57690 |
rs557846686 | snp | A/T | 6.59065e-05 | 0.00574012 | missense | TNRC6C | GRCh38.p7 | 17:78075235 | GCTGCCGCCCGCCAA[A/T]CTCCAAAGAGTCTTC | 57690 |
rs557901667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041795 | TAAGCCTTAGTAAAC[C/G]TATACTATCAACTGT | 57690 |
rs557905293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036652 | ACATAGGCCGGGCGC[A/G]TTGGCTCACACCTGT | 57690 |
rs557930792 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074726 | CAGAATAATCGGGAA[C/G]GCCCCTGCAAGAAAG | 57690 |
rs557949831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042451 | GTCAGCTAAGCCGAC[A/G]TGTATGGAAATACTT | 57690 |
rs557961360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010404 | TGTGCTTAGGCTCAT[G/T]CTAAACATATAAAGT | 57690 |
rs557965033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094766 | TCTTTAAAGTGATAG[A/G]CTTCTAAATGTGCCT | 57690 |
rs557982113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089119 | ATTACAGGCATGCAT[C/T]ACCACGCCTGGCTAA | 57690 |
rs558015170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102202 | ATCACCCCCGTCTCT[C/G]CTGGCACAGATGGGA | 57690 |
rs558023169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009720 | CCACCATGCCCAGCT[A/G]ATTTTTGTATTTTTC | 57690 |
rs558056825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017334 | CTGCTCTCCTGCTCT[A/G]TTCAGACCAGGGTGA | 57690 |
rs558078792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076535 | AAATTACTGTTATCT[A/G]AAATTCCAATGTAAC | 57690 |
rs558083506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063799 | GATCTGTGTCTATGA[C/T]GGTCAAAAGATAAAC | 57690 |
rs558085877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037198 | TCCTTTTCTTCCTAT[A/G]TGAGAATGTTCAGGC | 57690 |
rs558105075 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101681 | GTAGATACTAGATTA[A/C]CTACAAGTATCCCTT | 57690 |
rs558105645 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78004012 | CAGGGCAACCTGCAG[C/T]GCTGTTAGGGAAGTG | 57690 |
rs558125816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097588 | TAGGAGGCATGCCCC[A/G]TTTCTTCTTTCCCAC | 57690 |
rs558164580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096912 | GGATTGAGGTGCCTT[A/T]AGGATGGCCCATTTA | 57690 |
rs558173756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043026 | GCTTTTCTCTTTCTC[C/T]GTGAACCTGCATTGA | 57690 |
rs558281215 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031822 | CCGGAACACAGCATC[A/G]TCCCAGTAAGCTCCA | 57690 |
rs558346849 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055452 | CACAGTAGGTTTGTT[G/T]ACACGAGCATCACCA | 57690 |
rs558384069 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082102 | TGGCCAGCAGCCTGC[A/G]GTGCAACAGGGCTCT | 57690 |
rs558476628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070118 | AAATCAGAGCTCTCC[A/G]CTCATGAGGAGTAGA | 57690 |
rs558491361 | in-del | -/ATA | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018041 | GAAATCATTTTAAAG[-/ATA]ATGTCTCTTCTACTA | 57690 |
rs558500432 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024356 | GAGCAGTTTTTTTTG[G/T]TTTTTTTGTTTGTTT | 57690 |
rs558547610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037979 | TGATATAAAGAGAGC[A/C]GGGGGAAAAACAGAT | 57690 |
rs558556177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051707 | GAATGTTTTGGTGGT[A/G]GCGGTGGTGGCCTGG | 57690 |
rs558561219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011747 | ATGTTTCATTTTTCA[A/G]GAAATTGCACACAGC | 57690 |
rs558591330 | snp | A/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78051299 | CTGTAAACATGTGGG[A/G]TAGAAACAACCCGGT | 57690 |
rs558641127 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026300 | TGCTGTGCCAAATAC[C/T]GGGTACTGTGGATGT | 57690 |
rs558643592 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018106 | GTGTATATATATGGT[G/T]TTTGGTTTTTGGTTT | 57690 |
rs558677374 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057469 | AGTGGCATTACCCCC[A/G]GTGGCAGCCCCTTGC | 57690 |
rs558727825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045417 | TCCTGCCAGTATTGC[C/G]CCATTGGTGGTTATT | 57690 |
rs558728031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053177 | CGCTGCTGTTCTTAC[C/G]CTGGGCCTGTTTACG | 57690 |
rs558733426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065628 | GATTAGTTTTTGAAA[A/C]TATGTATTACCTCAC | 57690 |
rs558773100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078770 | AGGAGTTTGAGACCA[G/T]CCAGGACAACATGGC | 57690 |
rs558812635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052837 | TAGCCTCCAGCTAAC[A/G]CATCAGTGTCACTAA | 57690 |
rs558824072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091125 | AATTTAGGAATAATA[G/T]TCCTAGAAATACATG | 57690 |
rs558865440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077842 | TGGGTACAGGTGGAA[A/G]TCATCTTTCTAAATC | 57690 |
rs558947222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013820 | AGTATGACATTTTCC[A/G]TGAACTAAACAAACA | 57690 |
rs558948148 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104939 | AACCCAGCAGCGGCC[A/G]CCCTTTTGAGTACCT | 57690 |
rs558966347 | snp | A/G | 1.80971e-05 | 0.00300803 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064882 | CCCTGCAGAGCCGCC[A/G]GTGGCATTTGGAAGA | 57690 |
rs558977690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059898 | GCCCCCCGCCACCGA[C/T]AGCAGTAGGAAAGAG | 57690 |
rs559001057 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036407 | CTGCTGCTTTCCCAT[C/G]GAAGTAAGTGTTATA | 57690 |
rs559026155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079271 | TTCTCTTGGGTACAA[A/G]TTGACAGTGGTAGGA | 57690 |
rs559032774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013348 | GAGGGCTGGAGGCAG[C/G]AGGTACAGTTGGATC | 57690 |
rs559053813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072968 | TTAAGTTGATAGTGA[C/T]TAAATTGTTTGTAAC | 57690 |
rs559078360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092737 | AGAAGTTGTCTCAAA[A/T]AAATAAATAAATAAA | 57690 |
rs559160772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099587 | CATGGAAAAGACCTG[C/T]CCCCATGATTCAGTT | 57690 |
rs559188768 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017117 | TCAGGGAGGGAAAGA[G/T]AGGTGGGGCTTTGGT | 57690 |
rs559194296 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006602 | TTCTTCCTTCTTCCT[C/T]CTTCTTCCTTCTTCT | 57690 |
rs559201833 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040830 | TAAAATCCCATCCGT[C/T]CATGCCTCCGCCCCT | 57690 |
rs559226333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013131 | AAAAGAGTTGAAACT[C/G]TTTTTCAGCTCTTTT | 57690 |
rs559244810 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104987 | CGAACCTTGGCCGCA[A/G]TCCTTGCGAACTGTT | 57690 |
rs559257522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006016 | TGTACATGTAGACAC[A/G]TGCACTCTCACAGCT | 57690 |
rs559266819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006913 | GGCTCACTGCAACCT[C/T]CACCCCTCAGGTTCA | 57690 |
rs559346667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020314 | TGCATTATACTCCGG[A/G]ACCCTTGGTCTTTTT | 57690 |
rs559362720 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106118 | AGAATGGATGGTTCC[A/G]TGGAAGGAACAGAAA | 57690 |
rs559425552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067096 | GACTGTAATCCCAAC[A/G]CTTTGGGATGCCGAG | 57690 |
rs559430366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026660 | ACTGCTCAGGACCAC[A/G]TGGACCTTGCAGAGA | 57690 |
rs559432095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027118 | AAGGCAGGAGTGGCC[G/T]TCGCTGATAAAGACA | 57690 |
rs559432114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019446 | TCTCTCTATTTGGCC[C/G]TGTTATGACAACACT | 57690 |
rs559448998 | in-del | -/A | 0.203575 | 0.245652 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069209 | CCTAGAAACTGATTT[-/A]AAAAAAAAAATCAGC | 57690 |
rs559458711 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029394 | TACTATACTGAATAC[C/T]GTAGGCAGTTGCAAC | 57690 |
rs559476065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022924 | ATTCCATAAACAATA[C/T]AGTATAACAGCTATT | 57690 |
rs559476500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080969 | ATGGTGTCTTAGTCC[A/G]TTTGGGCTGCTGTAA | 57690 |
rs559495666 | snp | C/G | 0.000115931 | 0.00761264 | missense | TNRC6C | GRCh38.p7 | 17:78087034 | AGACTCCCGGCCTAC[C/G]TGACCTGCAGACCAA | 57690 |
rs559544872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006368 | AGAAGGGTCCAAAAG[G/T]TTTATGGTACATAGT | 57690 |
rs559561769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028759 | GTATGTACAGAACTA[C/G]GCATAAACTCATTTT | 57690 |
rs559607260 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013582 | TCCCACTCTCATGGA[C/G]CTGAGTCTTATGAGG | 57690 |
rs559648178 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053035 | ACATGGCAGCAGTCA[G/T]TCAGAGCCACTTGCC | 57690 |
rs559649279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059505 | CATGCAAAGGCCTTA[A/G]CTTTAGGTACCTTCA | 57690 |
rs559693510 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106741 | GTTTTGCAAGGAAGA[A/C]AGACAATGGAATAAC | 57690 |
rs559701147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021185 | GACAGTACTCAGGCA[C/T]CAGTAGCACAGAAAT | 57690 |
rs559724585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080245 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 57690 |
rs559765561 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082994 | AAACTACAGGTACAA[A/G]TAACTATTTTAACAG | 57690 |
rs559772853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074001 | GGTCAGTGAATTTTT[C/T]AGGATGTACCATATC | 57690 |
rs559788997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039707 | GCTTGCACACAAGGG[C/T]ATCCAGAGCAGACAG | 57690 |
rs559853143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014801 | CTCCAAATGTTGCCA[C/T]GGTGATAGATCAGCC | 57690 |
rs559883606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060957 | GTCCTATTTCTTGGC[C/G]TTTTCTCTGTCTGCT | 57690 |
rs559913810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046326 | GCTGGAACCACAGGC[A/G]TGCACCACCACACCC | 57690 |
rs559938072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008920 | TCTCCACTGCTCCCC[C/T]GCAGTTAGCACTCCT | 57690 |
rs559948842 | in-del | -/TGTGTAACAAACCTTCA | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012455 | TGACATGAGTTTACC[-/TGTGTAACAAACCTTCA]TGTGTAACAAACCTT | 57690 |
rs559954382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054730 | CAGACTACTACAGAC[G/T]ACTGTACACTACTGG | 57690 |
rs559963092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068765 | AGATCGCCTCACTGC[A/G]CTCCAGCCTGGGCGA | 57690 |
rs560008696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015425 | AGCATTTTTACCTAT[A/G]AAAAGTTAGTTTTAA | 57690 |
rs560012515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041822 | CTGTTGAAAGCATTG[C/T]GAACTAGTTTTTATA | 57690 |
rs560050424 | snp | G/T | 1.68823e-05 | 0.00290532 | missense | TNRC6C | GRCh38.p7 | 17:78049243 | ACAGGCTCCAGCTCT[G/T]GCCTGGCTCACTGCT | 57690 |
rs560052240 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041354 | ATGGCTTTCCCTACT[A/G]TGGTTTCTCTCTGCT | 57690 |
rs560052935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074842 | AGCCCCTGAGGGCCA[A/G]CAGTGGCTGGTGTGG | 57690 |
rs560057161 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054772 | GACTACTGTACACTA[C/T]TATACATTACTGCAG | 57690 |
rs560060875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029471 | AAAATACGCTATAAA[G/T]AATTTTTAAAAGGTA | 57690 |
rs560063462 | snp | C/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012670 | TTTCATGGCCAGTGG[C/T]GGATAGGGAGCCAGT | 57690 |
rs560072939 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092577 | TCAGGGCTGAAATTG[C/T]AGCTAACTGAAACAG | 57690 |
rs560091397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074480 | GTGGTGCAAACTGCC[A/G]GGGCGGGACAGAGCA | 57690 |
rs560098466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036232 | ACTCTTTGTGCCCTC[C/T]CCCCAGGTTTTAGTG | 57690 |
rs560098706 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065301 | AGACTGCCCTGAGCC[A/G]TGACTGTACCACTCA | 57690 |
rs560106868 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033920 | ACCACCCTTCACTGA[C/T]GAGGGGTCCCCTCAC | 57690 |
rs560118358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055055 | CACTGCAGAGTACTG[C/T]GCACCACTGTAGACT | 57690 |
rs560178684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070342 | TATGCTCCATGATAT[A/G]GCTGTGGCAGGCTCA | 57690 |
rs560184630 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062831 | AAGTATAACTTAGGA[A/C]TTCCCAAAAACTTAA | 57690 |
rs560197803 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069099 | ACTGTACATGACAGA[A/C]AATACCATAATCAAA | 57690 |
rs560206555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088573 | TAACTCCTAGGTTTG[C/T]TTTAAAGATTAAATG | 57690 |
rs560207315 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060790 | TGCCCATCACACTTA[C/T]AAAGCTATGTAAGTG | 57690 |
rs560220659 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025120 | AACTAAATGCCACAG[-/T]TTACATTAGGGTTCA | 57690 |
rs560225956 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066732 | AAACTCGATAGTCAC[A/T]TTGTAGCTCCATCTG | 57690 |
rs560230063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094307 | CACAGCATGCTATTT[G/T]GTGGAAGGAAGAGCT | 57690 |
rs560264176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101266 | TCTCTTTGCTAAAAC[A/T]ACAAGAGCCACCTTT | 57690 |
rs560265580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036718 | CACCTGAGGTCAGGA[A/G]TTTAAGACCAGCCTG | 57690 |
rs560271227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063182 | CCCGGGAGGCGGTGG[C/T]TGCAGTGAGCCAAGA | 57690 |
rs560286936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109259 | CAGAGGCATCATGGC[A/G]AGCCCCGACTGAGTG | 57690 |
rs560367003 | snp | A/C/T | 2.49801e-05 | 0.00353405 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071044 | AGAAATGCATTAAAA[A/C/T]GTAGCTCATGGACTT | 57690 |
rs560391332 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088594 | AGATTAAATGAGCTA[A/C]TATGTAAAGTTCTCT | 57690 |
rs560537143 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018600 | GAGTTTGAGCCCTTA[C/T]TTACCGTGCTTTCCT | 57690 |
rs560550189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023942 | TGGTGAAACCCCATC[G/T]CTACTAAAAATACAA | 57690 |
rs560614423 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030158 | TGCTAGACTTTTTTT[G/T]TTGTTTTTGGAGACG | 57690 |
rs560669467 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022269 | GACTCTTTAAAAATG[A/T]GTCTGTCTTAGATAT | 57690 |
rs560718661 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003639 | TATTTAGAAACAGAA[A/G]GAAGGTGTTTTCAAG | 57690 |
rs560727934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030778 | GCTGGAACCAGCAGC[A/G]TCAACATTGTCCCAG | 57690 |
rs560729273 | snp | A/G | 5.45103e-05 | 0.00522036 | missense | TNRC6C | GRCh38.p7 | 17:78050282 | GTTCTGGCAACCACA[A/G]TGAAGGAAGCACTGG | 57690 |
rs560753365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076908 | TTGCCATCCTTCCTC[C/T]GTGCTCCTACCTGAG | 57690 |
rs560783456 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011344 | TCTCCTCTGTCCCCA[A/C]CCTACCCCCATCTGT | 57690 |
rs560797986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056625 | CCCGCCACCACGCTC[A/G]GCTAATTTTTTTTGT | 57690 |
rs560802530 | in-del | -/CTACTGGAGA | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054669 | GCAGACTACTGTACG[-/CTACTGGAGA]CTACTGCAGACTACT | 57690 |
rs560816377 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102836 | ATTTTACAACTAGCC[A/G]TTCAAGAGTGGTTGG | 57690 |
rs560835801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083538 | AAATCTACCAATCTA[C/T]CAGATTTTATAATTA | 57690 |
rs560857433 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088633 | TTTTTTTCTCTCTCT[-/C]TTTTTTTTTTGGCTG | 57690 |
rs560876261 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021633 | GGAGTGCGATGGCGC[A/G]GTCTCGGCTCACTGC | 57690 |
rs560886886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012131 | TAATATCAGAAAATA[C/T]GCACTTTCAAATAGA | 57690 |
rs560910418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031114 | TCACACTTAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57690 |
rs560930595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078008 | TTTCTTAGGGATGAG[A/G]TTGACACACACACAC | 57690 |
rs560934889 | snp | C/T | 0.00109045 | 0.0233246 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102594 | TCCAGGGAGGGTTCC[C/T]GCTTGGCCCCCAATG | 57690 |
rs560966034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044952 | AATAGACATTGAGCC[C/T]AGGCAGGGGATGGCA | 57690 |
rs560970475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026375 | TAGTCTGATATTTAA[A/C]GAATAGCTGGGAATT | 57690 |
rs560972675 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103898 | ACTAACTTAATTCCC[G/T]CCTTAAAGACCCCAT | 57690 |
rs561099382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104410 | GGGGCCGTTCCCAAT[A/T]CAGAGAAAGCCAGTG | 57690 |
rs561138050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065019 | AGATTAGAGTTTTAG[A/G]ATACTTTCCTCATTA | 57690 |
rs561192248 | in-del | -/TAAAGT | 0.00636936 | 0.0560724 | cds-indel | TNRC6C | GRCh38.p7 | 17:78106043 | TTTCCATTTGGAATA[-/TAAAGT]TAAAGAGAAAAAAAA | 57690 |
rs561240066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039119 | AAGTTGGAACGTGTC[A/G]AGAGGCAGTAGGGAC | 57690 |
rs561282972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038571 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 57690 |
rs561309088 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078525 | TAATCACCACACATT[A/G]TTACCCTTTAATTTT | 57690 |
rs561331173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060102 | TAACCCTCAAACAGA[A/G]TCCCCTGACTTTGGA | 57690 |
rs561332362 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013863 | ATAGCAGGGTATGAG[A/G]TGAGGCCAAAGTGAG | 57690 |
rs561357981 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100445 | AACACCACGTGGAAG[C/T]TGCCAAGGCTTGGAG | 57690 |
rs561414541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067150 | GAGTTTGAGACCAGC[A/C]TGGGCAACATAGTGA | 57690 |
rs561489104 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107133 | CGTGTGCGTATGTGC[A/G]TCCGACATACCACTT | 57690 |
rs561503196 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027328 | CCATTTGTGAAGAGA[A/T]TAAATATTTGAACAT | 57690 |
rs561582865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093416 | CCCTGTGTGAAAACT[A/G]GCTTAATATGATAGC | 57690 |
rs561583564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085781 | GTTACTACCAGTGTT[G/T]CACATTGTCTGGGCT | 57690 |
rs561601711 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036714 | GGATCACCTGAGGTC[A/T]GGAGTTTAAGACCAG | 57690 |
rs561610393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027772 | CACATCCCAATGTAA[A/G]TGATGGTAACCTGTG | 57690 |
rs561671577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092771 | ATAAAGTCATTGATT[A/C]TTACAGAATCCTAGA | 57690 |
rs561687663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099710 | TTCTGCCCCTGACCC[C/T]TCCCAAATCTCATGT | 57690 |
rs561694049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060760 | TTTAACTAAAACTTT[C/T]CTCCCAAAAAGGACT | 57690 |
rs561727945 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022565 | CCCAGTGGTAGCTGG[A/G]TCAGTCATCTCAGCC | 57690 |
rs561793480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054122 | AGTTGTAGGACGATG[A/G]TAAGTATTTATATAT | 57690 |
rs561848101 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107278 | TTTGTTTGTTTTTTG[-/T]TTTTTTTTACCTTTT | 57690 |
rs561856324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100420 | TTCACTTCTGTGCAC[C/T]CAGAGTCTCAACACC | 57690 |
rs561905796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016169 | TATTGGCTCTCTTGA[C/T]TTCTAGAGCACAGTG | 57690 |
rs561909324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028913 | AGGTGGGACTGACTA[C/T]TGAGGCGCCGACTCT | 57690 |
rs561911877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009189 | TGGAGTAACTGGGGT[C/T]CAAGTGTCACTTCAG | 57690 |
rs561917576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074913 | GACTGCAGGAGCCAC[A/G]GAAGGGTGCCTGGGG | 57690 |
rs561950560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039253 | AGCCTGTGTTTGAGA[A/C]CCAGTTGAACTTTTG | 57690 |
rs561964613 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107083 | ATGGACATACACCTG[A/C]GTATGTATATCCAAT | 57690 |
rs561992132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015568 | GAAACAGTGGTATAC[C/G]TAGCTCATACCACAT | 57690 |
rs561992268 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108628 | ACAGACTGGGAACTC[A/G]GGGGACAGGAGGGCA | 57690 |
rs562058765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053591 | CTGAGATGGGGCCAT[C/T]GCACTCCAGCCTGGG | 57690 |
rs562077107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035159 | CATTCCAATGACTTT[G/T]TTTGATTTTGTCAGT | 57690 |
rs562122766 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099569 | TCACTATCACGAGAA[C/T]AGCATGGAAAAGACC | 57690 |
rs562125525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028419 | CAGGACCATGCATTC[A/G]TAGCAGTACCAAACT | 57690 |
rs562180364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074498 | GCGGGACAGAGCAGC[A/G]TGTGCTGCAAGAGGT | 57690 |
rs562218541 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060153 | CCACAAAGGCTTTCA[A/G]AAAAGTAGGATACTT | 57690 |
rs562247157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009861 | CCTGGCCTGAATTAT[G/T]ATTTTTAAGTCATAT | 57690 |
rs562255960 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086057 | TCAGCCATGGCTGGG[C/T]GCCGTGGCTCATGCC | 57690 |
rs562317904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030561 | CCATTATAATCTTAC[A/G]GAACCACTGTCATAT | 57690 |
rs562319115 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027971 | TGCGATCTCCGCTCA[C/T]TGCAAGCTCCACCTC | 57690 |
rs562322685 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071533 | GCTGGGACTACAGGC[A/G]TGAGCCACCATGCTC | 57690 |
rs562325103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061667 | CTTCAGCCCAGGCAA[C/T]GTAACAAGACCCCAT | 57690 |
rs562337557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069485 | AACTCCTGGGCTCGA[A/G]TTGTCCTCCTGCCTC | 57690 |
rs562352513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023716 | GAGGCTGAGGTGGGA[A/G]GATCACCTGAGCCCG | 57690 |
rs562402423 | snp | A/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78049288 | GATGGAAAAATGGAC[A/G]CTATGATTGGAGATG | 57690 |
rs562412717 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068871 | ATATACATGAGCTAC[A/C]TGAGACGTGTATCTC | 57690 |
rs562417775 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057381 | TCCAAACTTGTTAGA[A/C]CAAGCTATTATTTGA | 57690 |
rs562439925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036781 | ATACAAAAATTAGCT[A/G]GGTGTGATGGTAGGC | 57690 |
rs562463672 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082294 | AGTGAGGGATTTAGG[A/G]TCGTTTGATTATGAG | 57690 |
rs562468069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094975 | CAGAGGACAGGTGAG[G/T]CGCCAGCCAGAATCA | 57690 |
rs562476350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042552 | CTGCTCTTAAAATTC[A/G]GTCATTTCACAGATT | 57690 |
rs562488568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055126 | CATTTATTAAAAGAT[G/T]AAAAGATACTTTCTT | 57690 |
rs562518313 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024524 | GGTACCTGCCACCAC[A/G]CCCGGCTAATTTTTT | 57690 |
rs562526779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070500 | TGGTGCCGAGCCCTC[C/T]CCCACCCCCACTGCT | 57690 |
rs562540038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095682 | TGTGTTTAGGGATAC[A/G]TTAGGGTTTGTTATT | 57690 |
rs562554213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006075 | AATTTTCAAAGTTAA[C/G]GTTATGTGTATTATC | 57690 |
rs562575385 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047207 | CTTGGTCTTATTTTC[A/T]GTGTTAAATGAGGAA | 57690 |
rs562613269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076269 | TCACAAGCAAAGAAT[A/C]TCAGAGATGGGACTT | 57690 |
rs562642569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109299 | GAGGGAAAACAGAGA[C/T]AGTGGGGCATCCCGA | 57690 |
rs562666948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066029 | TGAGGTCAGGAGTTC[A/G]AAACCAGCCTGGCCA | 57690 |
rs562753168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046714 | AAGCTTTAAGAAGTT[C/T]TGCTTTTCCTAATTC | 57690 |
rs562778329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082685 | CATCCATTTATAGGC[C/T]CTCCCCAAGGGTCGC | 57690 |
rs562807253 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017832 | CACTGTCTAGGCTGG[G/T]GGGAGTGAGTTTGTA | 57690 |
rs562816391 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036761 | AACCCCATCTCTACT[-/A]AAAAATACAAAAATT | 57690 |
rs562827863 | snp | A/C/G | 3.32974e-05 | 0.00408017 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103597 | TCCAAGTAGCTCCCC[A/C/G]TCCCCCAGAGCATTA | 57690 |
rs562838589 | snp | A/G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074373 | GATTTGGGGGTTACA[A/G/T]ATTTTAGCAAGTAGG | 57690 |
rs562839023 | in-del | -/ATTTCC | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019625 | CAAAGAGTAACCAAA[-/ATTTCC]ATCTTGCTGAAAGTT | 57690 |
rs562869055 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008366 | TCTTTGGGTCATTTT[A/C]TTTTTAAGATTCAGG | 57690 |
rs562879090 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065603 | TAGATAAAACATGTC[A/G]TCTCCTTGAGATTAG | 57690 |
rs562889372 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039053 | GCTCTTTACTGACGA[C/G]TGAATGCTCTGCATT | 57690 |
rs562914563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102885 | GCTCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 57690 |
rs562918668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017609 | AAACTGGAGGCTCCA[A/G]GCTTCTCCTAGTGTG | 57690 |
rs562975096 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068458 | GAGTATTATAGGGTC[C/G]TGAGACCAAAAAGTT | 57690 |
rs563032453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043729 | CTTCTCCCCACCCCT[C/G]ACTCTCGCACTACCC | 57690 |
rs563050947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084566 | GCACAGAGCTCTAGA[C/T]ATGAGGTCAGGACCA | 57690 |
rs563068684 | snp | A/C | 1.68125e-05 | 0.00289931 | missense | TNRC6C | GRCh38.p7 | 17:78050827 | GATGGACAAAGATCA[A/C]ATCCAGCCTGGAGTG | 57690 |
rs563100238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044126 | ATGTTTTCAACATAG[A/T]TTCATAGTCTCAGTT | 57690 |
rs563107519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013488 | TCATTTGATCCAGCA[G/T]ATATTTATTGAGCAC | 57690 |
rs563107559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005308 | ATGTTATATTAGCTT[G/T]CCAAACAATGCTTTT | 57690 |
rs563147734 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026070 | AGTGAATCCAAGTTT[C/T]TGAGGTCTCTAGCCT | 57690 |
rs563186952 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105185 | ACTTTTCAGATTGTG[C/G]GCTGGAAAGGGTTAT | 57690 |
rs563209889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071947 | ACCACAGTCTGTTCA[A/G]TTCCTGAGATTGGAT | 57690 |
rs563216300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097184 | ATGCCTGTGAACAGC[C/G]ACTGTGCTGCAGCCT | 57690 |
rs563225012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104481 | CCCCATCTTGCTGTT[C/G]CAGGTGCGTCCTGGG | 57690 |
rs563268943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026568 | AAATGTGGTGGTTAG[A/G]TGAAGAAGCAAGCAG | 57690 |
rs563279133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072460 | AGAGACATGGAGATG[G/T]GCCTCACTGGGACAG | 57690 |
rs563282637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031970 | AGAGACAGACAAATT[C/G]ATTTCATTTTAAGTG | 57690 |
rs563349865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031169 | TTTTTGACACTGAAT[C/G]AGAAAGTCTGGAGGT | 57690 |
rs563371938 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068543 | TCACACCTGTAATCC[C/T]GGCACTTTGGGAGGC | 57690 |
rs563381282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097988 | AGGCCGTGTGGCGTG[A/G]TGAAGGATGGGTGGG | 57690 |
rs563385169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020227 | TGTAGACTACCAGCC[A/G]TAGCATTAGCATTGC | 57690 |
rs563437273 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054478 | TGCAGACTACTGCAC[A/G]CCACTGCAGACTACT | 57690 |
rs563442737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006225 | GTCCAGGTCTCTGAA[C/G]CTCTAGACTAGAGTC | 57690 |
rs563455855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098799 | CAGTTCCAGCACCCA[G/T]TGAGGGCCCACACTG | 57690 |
rs563491763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052397 | GCCATGTACTAGGCT[A/G]TACTCTAGTAGCTGG | 57690 |
rs563580664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027981 | GCTCATTGCAAGCTC[C/T]ACCTCCCGGGTTCAC | 57690 |
rs563670177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079630 | GGAAGTCACTATTTT[A/G]AAGTGAGAGCGGAGT | 57690 |
rs563672138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086660 | CGCTAATTGATGAAC[C/T]ATTAGATGATCATTG | 57690 |
rs563702026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039189 | GGTGTAGATAGCATT[A/C]GTCTTCCAGTGACCA | 57690 |
rs563708924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085812 | GTCCTGGACTTCAGT[C/T]TCCATCATTATAGAA | 57690 |
rs563716581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074409 | TTTACAAGTACAGAA[C/T]TCATGAATAATGAGG | 57690 |
rs563730773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014090 | GAGAGAAAATACCTA[A/G]GATTACTGCTATTTC | 57690 |
rs563740404 | snp | C/T | 3.33283e-05 | 0.00408204 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049989 | TGGTCCTGGAATACT[C/T]GCCTGGGGAAGGGGC | 57690 |
rs563801438 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052921 | CCTTTTTGGCCCACA[G/T]TTTTTCTGTGAATTG | 57690 |
rs563822527 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017895 | ACTCTACCTCGCTAA[C/T]CCTGACATACTTTTT | 57690 |
rs563825201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092085 | GGAACTCTTTACTGA[A/T]GGACACACGAGTAAG | 57690 |
rs563936657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081615 | AGTGCAGGGATCGGG[A/G]GTGACTCTGCCATAG | 57690 |
rs563937744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078604 | TTGCTGTTGTGTGTG[A/T]AACATTGTATGCTGG | 57690 |
rs563950495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014559 | CAAAGTAACCTTTTA[A/G]TGAAATGATTCTTAC | 57690 |
rs563981212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073827 | TTTCTGACCCTGGAT[A/G]ATGTGACCATAAATT | 57690 |
rs563984279 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080178 | GTTGCCGGGCGCGGC[A/G]GCTCACGCCTGTAAT | 57690 |
rs564041499 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017536 | CCCATGACTGCACAG[C/T]TGTTCAGCTCACCAT | 57690 |
rs564058116 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007805 | TGAATAATTTTGGTT[G/T]TGATAATTAGCTCAA | 57690 |
rs564068071 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054675 | TACTGTACGCTACTG[C/G]AGACTACTGCAGACT | 57690 |
rs564118856 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088024 | GACAAAGGGTTATCG[A/G]TAACTTGGAAAATAC | 57690 |
rs564129386 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036699 | GAGGCCGAGGCAGGT[G/T]GATCACCTGAGGTCA | 57690 |
rs564150126 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107334 | TCTGAGATTAAACAA[C/G]AAGTTCGTGGCTCTT | 57690 |
rs564205714 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078859 | CCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 57690 |
rs564208184 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086363 | AAAAAAAAAAAAACA[C/G]TATGTGTCAGCCACA | 57690 |
rs564244992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094222 | CCTGACCTCAGGTGT[C/T]GCCCATGCTGCTGGA | 57690 |
rs564252201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074934 | GTGCCTGGGGCCAAC[C/T]CCCATCCCCTTGCCG | 57690 |
rs564253831 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068669 | CGTGGTGGTGGGTGC[C/G]TGTAATCCCAGCTAC | 57690 |
rs564254926 | snp | A/C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005108 | TATTTAGGGGGGTAC[A/C/G]TTTATGGCGGTACCA | 57690 |
rs564275929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023801 | ACGGAAGTGAGACCC[C/T]GTCTCAAAAAACAAA | 57690 |
rs564295140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095757 | CTAACCAGAAAGCAC[C/T]AGCAGGCCGAGCACA | 57690 |
rs564325953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010708 | TGAAATATTAGATAT[C/G]TCTTTCTTTAGCTAT | 57690 |
rs564372088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008714 | TTGTAGTCAACTTTT[A/T]CTTATTTTTCCCTCC | 57690 |
rs564402842 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054506 | ACTGTACACCACTGC[A/G]AAGTAGAGTTCACCA | 57690 |
rs564420563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087477 | AGCAGGAGTTTTGCC[A/G]CTGCCAATAATACTC | 57690 |
rs564421328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101936 | ATGGCCAGTTTTGGG[G/T]CCAGTTTAATGGCCA | 57690 |
rs564431913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78047431 | CCTGGAATTACGTAC[C/T]TACTTTGAAATCACC | 57690 |
rs564485728 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060212 | AGCAAACTCTTCTAT[A/G]TAAAGTTTCATTGTA | 57690 |
rs564509976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029413 | GGCAGTTGCAACACA[A/G]TGGTAAGTATTTATG | 57690 |
rs564545913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023147 | AAAATTAAAAATTAA[C/T]AACATAACGTATGCG | 57690 |
rs564547810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028944 | TGCACTTTACATGTC[A/G]GCGTGCAGAATTACT | 57690 |
rs564578731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068946 | ACTGAATTTCAAGTA[C/G]GTCACAAACTTAAAT | 57690 |
rs564585187 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089604 | CCTGTCGTTGTTATT[C/T]TCAGTCTTTTGCCAC | 57690 |
rs564596140 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033583 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAC | 57690 |
rs564608342 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074753 | AAAGCAACCACTGAG[C/G]CCACCCGAAATGAGG | 57690 |
rs564662360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002876 | ATTGAATTAGTGAAC[A/G]TATGAGATGGACTTG | 57690 |
rs564685192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055701 | AAGAGTTCAGGCTAC[A/G]GAGGGCCCTATGCCT | 57690 |
rs564690728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025570 | GCAGGTTTTTGTATG[A/G]ACGTAAAGTTTTCAA | 57690 |
rs564732588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036893 | CACACCACTGCACTC[A/C]AGCCTGGGTGACAGA | 57690 |
rs564753270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063158 | GACTGAGGCATGAGA[A/G]CCCCTTAACCCGGGA | 57690 |
rs564777878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031051 | TTGCAGTGAGCTAAG[A/G]TGGTGCCATACTGCC | 57690 |
rs564783491 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109224 | GAAGGCTGTTCCAAT[C/G]GGGGAGAAGCCAGCA | 57690 |
rs564834731 | snp | A/G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030243 | CAACCTCCACCTCCC[A/G/T]GGTTCAAGCAATTCT | 57690 |
rs564883794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017806 | CTTTTCCATTTCAGG[A/G]CCTTCCCATGCACTG | 57690 |
rs564887063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083364 | TGTAAATGTTTTGGC[C/T]TCTTTGTTTTTGTTT | 57690 |
rs564897344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043429 | AACATATTTTTTATA[A/T]TTTTTTTTATTTCTG | 57690 |
rs564923263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089878 | GGCCTGGCTTGTTTC[A/G]GGGGCCCATTTTGCA | 57690 |
rs564951028 | snp | A/G | 0.000126735 | 0.00795935 | missense | TNRC6C | GRCh38.p7 | 17:78051428 | GTACTCAGCTGAATC[A/G]ATCACCGTTGCTTGG | 57690 |
rs564998334 | snp | C/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78050102 | AATGGGGAAAGCCCC[C/G]AAACCAGCATTCCAA | 57690 |
rs564999499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099954 | AAATTGGCCAAAACA[A/G]AGGGGCTCAGGCCCC | 57690 |
rs565023371 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036931 | TCCATTAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAT | 57690 |
rs565060355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071687 | GTCACTACGCCCAGC[C/T]GGAAAATGCTGTGTG | 57690 |
rs565077336 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057110 | CACAAATTTTTTTCC[A/G]TGTGGAAGTGTGCTC | 57690 |
rs565140729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070951 | GAGTTTCTGGAATAC[A/G]GCATTATTCAATGTT | 57690 |
rs565179444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076733 | TTCTGTCTTTTATTA[G/T]TTCTATAACTCACCC | 57690 |
rs565204594 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009160 | GCCATTAACTTGTGC[A/G]TTGTAGCTCTCTGTG | 57690 |
rs565235835 | snp | G/T | 0.00151932 | 0.0275201 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097846 | AGCAGCATTGCATCC[G/T]CACCTAGTGTTGCAG | 57690 |
rs565245006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011565 | AGGTGTATCACAGCT[A/G]TTTATCCTCTTCATT | 57690 |
rs565264042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044364 | TAAGAATTATTCATT[C/T]ATTCAATGTATGTTT | 57690 |
rs565265894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052138 | GAGCGCTGCACAGGT[A/G]GGCCAGGCTGTCATG | 57690 |
rs565267834 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039392 | GCCGTCACCCACGTT[A/G]GCCTGGGCATTGGGC | 57690 |
rs565300614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098076 | TGGTAACGTCTTCTC[C/T]ATACAAGTGTGTGGG | 57690 |
rs565322377 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097237 | TCTCTTAAAAAAAAA[A/T]TTTTTTTAAGCAAAA | 57690 |
rs565326866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085465 | TTCTAATAGTATAAT[A/C]TCCACCTTTATTTGG | 57690 |
rs565359072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103812 | TCTCTTTGTGCATGT[C/G]TGTGCCGTAATCTCT | 57690 |
rs565415551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064942 | GTGCAAACCAGGTAA[A/G]CCTAGCATCCTGCTT | 57690 |
rs565425843 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104020 | TCTTGGGACTTACTG[G/T]TTTTTTTCTGCTGCT | 57690 |
rs565445303 | in-del | -/AAC | 0.181978 | 0.240568 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106532 | TATTTAAAAAAAAAA[-/AAC]AAAACAAAACAAAAC | 57690 |
rs565445802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032016 | TTGTGTTTTCCCTCT[A/G]TTTATTTACATTATT | 57690 |
rs565480114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038534 | AATACAAAAAATTAG[C/T]CGGGCGTGGTGGCGG | 57690 |
rs565520324 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096620 | GCCTACGGCTGAGAT[A/G]CCATGGCTTTTCAGA | 57690 |
rs565525873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058779 | GGGATTCCAGCTGTG[C/G]TGGTGGTGACCACTG | 57690 |
rs565542647 | snp | A/G | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78104624 | CAGCCGCGGCTCAGC[A/G]CAGCGGGCAGCTCCC | 57690 |
rs565584233 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099037 | TCTCATAATATTGCA[C/G]CTTCTCTCAGGTGCT | 57690 |
rs565589941 | snp | C/T | 1.76502e-05 | 0.00297066 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091423 | CAGGCGAATCCTAAC[C/T]GCATCTCTCTCTTTA | 57690 |
rs565599867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005084 | AAAAACCAAAGGTAA[A/G]TTTATTTATATTTAG | 57690 |
rs565632103 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107820 | GAGTGCCACTCACTT[C/T]TGCCTAGGGTCCAGT | 57690 |
rs565701706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012239 | CTAGAGATGGCTAGT[C/T]AATTCATTAATTAAC | 57690 |
rs565704813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028021 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTGC | 57690 |
rs565740494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058093 | AGGGCTCCAGAGGCC[A/G]CACTTGACACTCCTC | 57690 |
rs565748016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018747 | GTTCCTTGATACAGC[C/G]CCAGCCTAGAGGAGG | 57690 |
rs565773280 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084216 | TTGAACCTGGAAGGC[A/G]GAGGTTGCAGTGAGC | 57690 |
rs565777998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065276 | AGAATTGCTTGAGCC[C/G]GGGAGGTTAAGACTG | 57690 |
rs565856420 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068979 | TAAAAATATGAAAAC[A/G]TGAAAGAACATTAAA | 57690 |
rs565909796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084960 | CCATCTGTCAGAAGG[A/G]AGGTGGTGCTGTAGT | 57690 |
rs565972665 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103990 | AAGGCGACACAGGTC[A/C]GTTCCTCACAGGTAT | 57690 |
rs566003859 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053192 | GCTGGGCCTGTTTAC[A/G]TTAACTGACTGGTTC | 57690 |
rs566012881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021551 | TATGGAGAGGAGACA[C/T]GGAATAGGTTATTTA | 57690 |
rs566028072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044584 | CAGCACAGTAGCTGC[A/G]TATAGGAGGCACTCA | 57690 |
rs566070896 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066863 | CCAGCTGACTGTCAC[A/G]AGTGGACAGGTTTGA | 57690 |
rs566076825 | snp | A/C | | | missense | TNRC6C | GRCh38.p7 | 17:78049447 | TCCAGTATTTGCAGT[A/C]CAGTCAGTGCCATAG | 57690 |
rs566128071 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073326 | CATGTTGGCTTTTCT[C/T]ATATTTTCCCGTTAT | 57690 |
rs566135278 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023670 | AATTAGCTGGGCATG[G/T]TGATACACATCTGTC | 57690 |
rs566184904 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101074 | AGCCACCGTGCCTGG[A/C]CAATTTTCTGAACTT | 57690 |
rs566186203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014238 | TAGCATGAAAAGAGA[C/T]GTGGTCAAGAAGGAG | 57690 |
rs566199128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032347 | TTCCTTGCCTGTAAC[A/T]AGTTGTTAGCTTTCT | 57690 |
rs566214949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060411 | AGTACCTTAAAAAGC[C/T]AAGCACATAGCAAGC | 57690 |
rs566231357 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106369 | CGTCGTGGACTCTGT[C/T]GATTGCTTTCGCCCC | 57690 |
rs566242209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100552 | GCACCAAATTCCTAA[A/G]CTGCACACAGCATGT | 57690 |
rs566318073 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019595 | TTAAAAAACAAAAGG[C/T]AAAAGCTTACTAGGC | 57690 |
rs566356978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013855 | GCTATGAAATAGCAG[G/T]GTATGAGGTGAGGCC | 57690 |
rs566357846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074998 | CTAGCAAAGCAAGGG[A/C]TCTCTCTGCCCCTGG | 57690 |
rs566359638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068388 | CTAATACAGTAAATA[A/G]CAATAGACACAACTC | 57690 |
rs566371565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059905 | GCCACCGATAGCAGT[A/G]GGAAAGAGTTAGCCC | 57690 |
rs566379120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067458 | CACCTTCCCTGGTGG[C/T]CCCAGGATTTGTTCT | 57690 |
rs566387462 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107776 | CGGCAGCAAGAAGAT[A/G]CCGGGGCTTGCCTGG | 57690 |
rs566391812 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050613 | GCCACCTGCCGCTGT[A/G]CCAGCAAACACAGGT | 57690 |
rs566472774 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066812 | AGAAATGCAGCCTGT[C/T]GGGCCCAACCTCAGG | 57690 |
rs566474602 | snp | C/T | 0.000252319 | 0.0112292 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050019 | CAGTGGCAACAATGG[C/T]GTTGGTAATATCCAT | 57690 |
rs566487759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088232 | TAGACTAGATGATCT[C/T]GTTCCTTAATTATTG | 57690 |
rs566489739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095060 | ACAGGAAAATTAGCA[C/T]ATTTTGAGGGATGTG | 57690 |
rs566497153 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092642 | TCCAGCTACTTGGGA[A/G]GCCAAGGTGGGAGGA | 57690 |
rs566504533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080583 | CATTTTACAATTTTA[A/G]GCTTTGGACCAAGTT | 57690 |
rs566565579 | in-del | -/AAGG | 0.000277836 | 0.0117831 | splice-donor-variant | TNRC6C | GRCh38.p7 | 17:78077336 | TTCTTCTAGACAGGT[-/AAGG]AAGGCTGTTTGGAGA | 57690 |
rs566570064 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007998 | GGAACTTTTTAGAAT[A/C]TATGACATGCTCATC | 57690 |
rs566575144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094526 | TCACTGCAACCTCCG[C/T]CTCGCAGGCTCAAGT | 57690 |
rs566602518 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006819 | TTTCTTTTATTTATT[C/T]ATTTATTTATTTTTT | 57690 |
rs566609546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054336 | CACTGCAGACTACTG[C/T]ACACTACTGCAGACT | 57690 |
rs566647570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028602 | CAATGTAGCGTTCAC[A/G]TGGTAGATGGCCAAG | 57690 |
rs566660671 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009494 | AAAGTTAATCTTACC[A/C]TGTATGAAAGTGAAT | 57690 |
rs566667874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028982 | TCACTGTTTGCATTC[A/G]GCATGCTAATTAGTA | 57690 |
rs566667979 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107679 | ATCTTAATCATCATC[A/G]AGAGGCACAGCCAAG | 57690 |
rs566679047 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042985 | CTAAGCCTACCCTTC[-/A]AAAAAAGAGCTTATA | 57690 |
rs566685653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034923 | GCAGTGAGCCAAGAT[C/T]GAGTCACTGCATTCC | 57690 |
rs566753855 | snp | A/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002254 | ATTTCAGCTGAGATT[A/T]TATACCAGAAATTGG | 57690 |
rs566764476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089553 | CCCATGGTCAGTAGT[A/G]GGGGCTCCTAGCTAC | 57690 |
rs566778100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081664 | GGAAAAGGCAGCACT[A/G]CTGTGCCGGTGGCCT | 57690 |
rs566782329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009472 | GATGTTTTCATACAA[A/G]AAGCTCAAAGTTAAT | 57690 |
rs566787374 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037612 | TGAAAAGCGCAGACC[C/T]GCAGTTGTAAAGCCT | 57690 |
rs566809575 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087515 | AAAACCTTTAAAGGT[A/T]GTACCAGTCAGAGCC | 57690 |
rs566818515 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015444 | AGTTAGTTTTAAAAT[A/G]TACTGCTCTCATCCA | 57690 |
rs566823229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054887 | CTGCAGACTACTGTA[C/T]GCTACCATACACCAC | 57690 |
rs566826649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010007 | CCCAACCTCAGCCTC[C/T]CAAGTAGCTGACTAC | 57690 |
rs566837411 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101561 | CAGAAATAGAGCGGT[A/G]TGAAGTGGGAAATCG | 57690 |
rs566841040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055332 | CTCCACACGTTGTCC[C/T]ATTGGAGATCCAATA | 57690 |
rs566845996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089021 | TGCCCAGGCTGGAGT[A/G]CGATGGCGCAGTCTC | 57690 |
rs566863390 | snp | A/C | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105953 | ATCTCTGGAGAAATA[A/C]CATGTATACCTACCT | 57690 |
rs566894253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025125 | AATGCCACAGTTTAC[A/G]TTAGGGTTCACTCTT | 57690 |
rs566926945 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078968 | TATGGTGGCAGGCGA[C/T]GGTAATCCCAGCTCC | 57690 |
rs566928794 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78062720 | TGAAGTGTGAAGGGC[A/C/G]TGGGGAAATCCTTCT | 57690 |
rs566931553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024657 | GGCGTGAGCCACCGC[A/G]CCTGGCCTATTTAGA | 57690 |
rs566942679 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108813 | TTATTAAATTTTTTT[G/T]TAAATGGCAGTTTCA | 57690 |
rs566974355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016218 | GGTCAGGAAGCGGCA[C/T]TAACACTGTCTCTCT | 57690 |
rs567009128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082840 | CTCATTCTGGCAGCC[A/C]AACCTTGCATTGTCT | 57690 |
rs567033238 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083814 | TTCACATAATCTTGA[-/T]TTTTTTTTTAATTTT | 57690 |
rs567036555 | snp | C/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012587 | GTATATGCAAATGAA[C/T]GCAATAAAATGTTCT | 57690 |
rs567037488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052865 | TAAACCAGAGGTCAA[A/G]AATCAGTGGTCCGTG | 57690 |
rs567094826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042765 | TGCTGGTGGTGATCA[C/T]GGTGGTGGTGCTGAT | 57690 |
rs567114253 | snp | C/T | 2.02206e-05 | 0.00317961 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104719 | TGAGCTGCTGTGGGG[C/T]GGGGTGCCCCAGTAC | 57690 |
rs567125959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102660 | GGTTCTTGGTCAGGG[C/T]CCATAAGTGACGCTG | 57690 |
rs567181283 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046185 | CGATTTTTAGGATTC[-/T]TTTTTTTTTTTTTTG | 57690 |
rs567207702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017915 | ACATACTTTTTCAGG[C/T]TCTGCTTAATTGTCA | 57690 |
rs567216455 | snp | C/T | 1.6574e-05 | 0.00287867 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049512 | AGGCACTTTAGGTGC[C/T]TGGGGAAACTTGCTG | 57690 |
rs567265477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063684 | TCAGATCTCTCTCAG[C/T]TTGTGGGTGGTACCA | 57690 |
rs567285248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029797 | TAACTTTTAAACTTA[C/T]TAAAAACCTAGACAC | 57690 |
rs567309189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097298 | CAGAAGAAATACTCA[A/C]ATTTTTATGGCAAAT | 57690 |
rs567319037 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059321 | TTTTTGTGGATGTGG[A/G]ATTTTTCTTGGGTTT | 57690 |
rs567350421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030296 | CTGGGATTACCCGTA[C/T]CTGCCACCACACCTG | 57690 |
rs567426639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090290 | TTAGACAGGACAGAC[A/T]CTCTCTGGTTTGCCA | 57690 |
rs567438492 | snp | A/C | 0.000167347 | 0.0091458 | missense | TNRC6C | GRCh38.p7 | 17:78050991 | CAGTGGCTGGGGCAA[A/C]AGCACAAATACAAAG | 57690 |
rs567439839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010972 | GGGCGCTGTGCTCCG[A/G]GGGCGCCTCCCGAGG | 57690 |
rs567456300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056251 | CAACTTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 57690 |
rs567502103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066155 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 57690 |
rs567516899 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096644 | TTTCAGAAACCGTCC[A/G]ATTCTGTTTATGGTC | 57690 |
rs567627417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072100 | ATGAGTCCAGAATGG[A/C]CTCCATGTAGCGGAG | 57690 |
rs567632425 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108432 | GGCAACCCTCAGCTC[C/T]GCGCGGCCGAGCCTC | 57690 |
rs567644990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078471 | GTTGAAATAATAACT[A/G]TATTTCCTGTTTGAA | 57690 |
rs567660689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004483 | GTTAGAGCTGTGTTT[C/T]AAGGAAGCTGTGTTT | 57690 |
rs567674732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083862 | TTTACTATAATTGCC[A/G]TGTCATTGTATACCT | 57690 |
rs567680548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092253 | AAGAAAAAGGAAACT[A/G]TGTCTCATGGTTAAC | 57690 |
rs567699268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051585 | AAGTTCCCTATCACC[A/G]TGCAATATTGTATCT | 57690 |
rs567715034 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100029 | AAAATGATCTTTGAC[C/T]TCATATCTCGCATCT | 57690 |
rs567718319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78029273 | TCTGAAAAATGCACC[A/G]TTAGGCTGTTTTGTC | 57690 |
rs567766420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091709 | TTTCTAAGAATTGAG[C/T]ACTGAAAGTTGGATT | 57690 |
rs567832779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072651 | ACTTTGGGAGCCCAA[A/G]GCAGGAGAACCACTT | 57690 |
rs567833204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019618 | TACTAGGCAAAGAGT[A/T]ACCAAAATTTCCATC | 57690 |
rs567861731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78032145 | AGTTACTTTAGAACC[C/G]AGAAGTGAAAACTTT | 57690 |
rs567863700 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070376 | GTGAAAAACACTATG[A/G]AGAATATTTTTGGAA | 57690 |
rs567872661 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078969 | ATGGTGGCAGGCGAC[A/G]GTAATCCCAGCTCCT | 57690 |
rs567885672 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073000 | TTTCCTTTTGTTAAT[C/T]AATGTGCACTAATGA | 57690 |
rs567913419 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031175 | ACACTGAATCAGAAA[A/G]TCTGGAGGTTGGCAC | 57690 |
rs567930905 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006522 | CTTCTTCTTCTTCTT[C/T]TTCTTCTTCTTCTTC | 57690 |
rs567945920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086773 | TCAGCATAAAGACAA[C/T]GAAGAATGCATTTGG | 57690 |
rs567962227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069697 | ATGTCACTTCTACAT[C/T]ATACAGAACTAAAAG | 57690 |
rs567987044 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031559 | CCAGCCCCAACCTGC[C/T]GGTACCAGTACCAGT | 57690 |
rs568012791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098949 | TATATTTGCTTCTCC[A/G]CAAGATGTCACTGGG | 57690 |
rs568087742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014392 | CAGTAGGCATTAATG[A/C]TGTCTTGATTACTCA | 57690 |
rs568102628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052571 | CTGCATGCGGGGGCC[A/G]CTGGAGTTGGGGAAT | 57690 |
rs568242320 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073601 | GTCGATTCTTATTTT[C/T]TTGGTAGTTATGTTC | 57690 |
rs568267225 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087459 | ACTAACCACGTTGTA[C/T]AGAGCAGGAGTTTTG | 57690 |
rs568278751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079766 | TGCTCCTTGGAATGC[C/G]TCAGCCACCGAAACT | 57690 |
rs568342760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008168 | CTTATTTAAAAGACT[A/G]ATGCCGAACTGAAGC | 57690 |
rs568374473 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78021570 | ATAGGTTATTTATTT[A/T]TTTATTTTTATTTTC | 57690 |
rs568412675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100143 | GCTGGTATTGTCTGC[A/G]GCTTTTCCAGGCACA | 57690 |
rs568424845 | snp | A/C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081671 | GCAGCACTACTGTGC[A/C/T]GGTGGCCTTGAAATT | 57690 |
rs568445837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060446 | AATAAATGCCTGATC[A/G]ATTGCATTTTTAATC | 57690 |
rs568446289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068002 | TATCCAGTTAATCAG[A/G]CAAAAAGATAGACCT | 57690 |
rs568459252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028041 | GCTGGGACTGCAGGC[A/G]CCCGCCACCATGCCC | 57690 |
rs568596902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094382 | CCCAAAACATTGAAT[G/T]TCCCACTTGAAATAT | 57690 |
rs568602043 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035023 | CTGAACCATAGGTGA[C/G]GACTTGGAAACTAGA | 57690 |
rs568602151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78041390 | GGCACGGGCAGGCCT[C/T]CCCAAATTAGGAAGC | 57690 |
rs568605595 | snp | C/G | 0.000198936 | 0.00997137 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093784 | GGTGCTGCTCTTCCT[C/G]CCTCTGCATGGACGG | 57690 |
rs568615449 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054437 | CTGCAGACTACTGTA[A/T]ACCACTGCAGACTAC | 57690 |
rs568640645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040855 | GCCCCTAGTTGAAGG[A/G]GATGAGTCGGGTGCC | 57690 |
rs568641733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78100833 | CAGGCCGGAGTACAG[C/T]GGCGTGATCTCGGCT | 57690 |
rs568668359 | snp | C/T | 0.000139506 | 0.00835068 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067946 | CAACACTCTTAACGA[C/T]GGTACACCCTGAAAA | 57690 |
rs568704113 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056008 | TCTCCCCTTTGATAC[A/G]TGATCCTTAGAAACT | 57690 |
rs568726548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007441 | ATTGCCTGAGAAATA[C/T]TGGTTCCAACTTTCT | 57690 |
rs568755435 | snp | G/T | 1.99515e-05 | 0.00315838 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075173 | GGACGTGGACAAGCG[G/T]GGGCTGGGAGTGACC | 57690 |
rs568818619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038047 | GGTTCAGATCAATAT[C/T]GAGTGCTAGAAAGCC | 57690 |
rs568832447 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040990 | CTGGCAGCTCTACAG[C/G]AGGCGGCTCTCGCTG | 57690 |
rs568899497 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069505 | CCTCCTGCCTCAGCC[A/T]CCTGAGTAGCTGGGT | 57690 |
rs568930478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102145 | GGGTCTGGGGACAGG[A/C]AGAGGTGGAGAGCAG | 57690 |
rs568936055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024528 | CCTGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 57690 |
rs568957782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089051 | CGGCTCACTGCAACC[G/T]CCACCTTCTGGATTC | 57690 |
rs569044113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023997 | CACCTGTAATCCCAG[C/G]TACTTGGGAGGCTGA | 57690 |
rs569047214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016355 | CACTCACATGTAACT[A/G]GGGGAACCAGATCCC | 57690 |
rs569049382 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058261 | GAAAGGGAGAAAGTG[C/G]AAACATAGCATTTAT | 57690 |
rs569066756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069144 | AGCAAACTGGAAAAA[C/T]ATGTTTATAACTCAT | 57690 |
rs569087644 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070027 | TTATACTTTTGAATC[A/G]TGTGAATGTATTCAT | 57690 |
rs569141896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075673 | AAGTGGTGGGGCTTG[A/G]GCACCCATCTCTGGC | 57690 |
rs569148994 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054906 | ACCATACACCACTGC[A/G]GACTACTGTATGCTA | 57690 |
rs569168559 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108344 | GAGTGGGACCTAATC[C/T]GGAGAAGAAATTAAA | 57690 |
rs569171638 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78104234 | TGCAAATGACACTGA[C/T]CCTAAACGAGCCCAC | 57690 |
rs569234379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082924 | TTTTATTCCATAGCA[A/G]TAGTTTCAGGGGGTC | 57690 |
rs569235270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78095234 | AGTGGCCTCAGCCAT[C/T]GCCTGAGTGTGCCAT | 57690 |
rs569253210 | snp | A/G | 0.00028884 | 0.012014 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050310 | TGGGAGGGAAGGAAC[A/G]GGAGAAGGCCGAAGG | 57690 |
rs569285035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011699 | CTTGAGTAAATGTAT[A/G]ATAGTAAAATGGCTA | 57690 |
rs569300780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010927 | AACAAATTGTGAAAC[A/G]AAGGAAGTGAGCCTA | 57690 |
rs569318901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102595 | CCAGGGAGGGTTCCC[A/G]CTTGGCCCCCAATGC | 57690 |
rs569362827 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010355 | TAGTCTTCAGTTGAG[G/T]GATGGAGGTTTTAGA | 57690 |
rs569508392 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081830 | AAGGCATCTGTGTGC[C/G]GTCTCACTGTTTCTT | 57690 |
rs569560993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037176 | CTTCACACTTTTTCA[C/G]TCTTTTTCCTTTTCT | 57690 |
rs569602921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012159 | AGAATCACATTTTAT[C/G]TAGCTTTTAGCATAA | 57690 |
rs569625520 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003930 | CTTATCCCCAGCAAT[G/T]CCTGATGATGGGTTG | 57690 |
rs569631584 | snp | A/G | 0.0093238 | 0.0676385 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104887 | GCCGACCCCTCCCGG[A/G]ACCCCTCCCGGCTGG | 57690 |
rs569646460 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057441 | TCCCTTCATAGAGGT[G/T]ACAGCATGCAGGAGT | 57690 |
rs569827404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084347 | AAAAAAAAGAATGGG[A/C]ACTCCAAAAGACAGA | 57690 |
rs569840578 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038390 | TGAAAGTATTCCCTT[G/T]TGGCTGGGTGCGGTG | 57690 |
rs569852054 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098050 | CACATCAGCTTGCAC[A/G]CACATGGAAGTGGTA | 57690 |
rs569879765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091049 | TATTCAGCACTGAAA[C/G]AAGTAAAATGAAGAG | 57690 |
rs569886294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051679 | ATTAAGCACACTCAG[G/T]AGAACATCAAGCGAA | 57690 |
rs569938202 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063340 | AGGTGGAATTGGATC[A/G]TCATAAAGGTCTTCA | 57690 |
rs569978379 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059047 | TATTGTTTCTATAAG[A/T]CTCATTAGCAGCAGA | 57690 |
rs569992402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027471 | CTTTTTTATATTCAG[G/T]TCCATCATATGGAAA | 57690 |
rs569998166 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026735 | AACCAGGGAGGAGAT[C/G]TGCATTTCAGAAGGA | 57690 |
rs570004739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058004 | AGGTTCATTCTGGAG[A/G]TAAAACAACAGTATT | 57690 |
rs570057963 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100874 | TCTGCCTCCCAGGTT[-/C]AAGTGATTCTCCTGT | 57690 |
rs570058678 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072590 | CTCAGTGTTGTACAG[A/G]ATGATTTTAGGACCA | 57690 |
rs570096080 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098966 | AAGATGTCACTGGGA[C/T]GTAAGGCTTTTGCAG | 57690 |
rs570129126 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051992 | AGATTTTAAGGTGGC[A/C]AAGTCGTGAGCATGT | 57690 |
rs570152486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086203 | GGCGTGGTGGCACAC[A/G]ACTGCAATCCCAGCT | 57690 |
rs570186599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084853 | AGGCTGCTGGTCTCC[A/C]ACTCCTTACCTCAGG | 57690 |
rs570227957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016541 | ATCTAGCGCCTAACA[C/T]TTTCCAAACTGTTGG | 57690 |
rs570236946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013792 | CATCTGTAAAGAGCC[C/T]GTGGCCGTATGGAGT | 57690 |
rs570253353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053169 | CAAGCTTGCGCTGCT[C/G]TTCTTACGCTGGGCC | 57690 |
rs570265137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073521 | AAGATTTTCTGTCAA[A/G]GAACAAGCAACCCTA | 57690 |
rs570297169 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048742 | GTTTGTCATTCAGAT[C/T]TGAAGACTTGAAATA | 57690 |
rs570297885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78013021 | TAAGTTTGCTATGAA[A/C]GCAAGGACAAGGAGG | 57690 |
rs570306461 | snp | A/G | 0.000150727 | 0.00867991 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086858 | TGCCTGCCAGGTTGC[A/G]CGCACAATCACTAAT | 57690 |
rs570311826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074613 | CAGTGTCTGTTTTGC[A/G]CAGTATTGTATCCCC | 57690 |
rs570330813 | in-del | -/ACCCCTCCCGGC | 0.000798881 | 0.01997 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104887 | CCGACCCCTCCCGGG[-/ACCCCTCCCGGC]ACCCCTCCCGGCTGG | 57690 |
rs570338008 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074186 | TTAAACACCAGAATC[A/C]CTACAGAAAGCACAG | 57690 |
rs570349053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081200 | TCCAATTCATGGGGG[C/T]TCCTGATCACCTCCC | 57690 |
rs570366601 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076140 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 57690 |
rs570394783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092869 | AGGGAGGCTTAGGGT[A/G]TCTTCTGGTGTCTCT | 57690 |
rs570429045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080479 | GAAAAAAGGTCAAAT[C/T]GAATTAAGGAAAAGG | 57690 |
rs570441873 | snp | A/C | 0.00809048 | 0.0630855 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039319 | ATCTTGCCCCCCCCC[A/C]CCACTCCCTACCTCT | 57690 |
rs570454796 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089057 | ACTGCAACCTCCACC[C/T]TCTGGATTCAAGCAA | 57690 |
rs570478679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045831 | GAAAATATTTTTTCA[A/G]TAGAAGAAAGTATAT | 57690 |
rs570507322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092371 | TTTTAACATCCACTG[A/T]GTTCTTCCGTAGTGA | 57690 |
rs570511787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78007125 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT | 57690 |
rs570515338 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108257 | CACAGGCTGGCCCCC[C/T]CCCACCCATGGGGAA | 57690 |
rs570548490 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003571 | AAAAGAGTAGAAAAC[A/G]TAAGAGAAACAACAA | 57690 |
rs570573516 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006590 | CCTTCTTCTTCCTTC[C/T]TCCTTCTTCCTCCTT | 57690 |
rs570614121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067683 | CCCACGACCCCTAAA[G/T]TATATGTTACAGTGG | 57690 |
rs570617486 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084001 | AAAATGACCAGGAAT[C/T]GGCCGGGCACGGTGG | 57690 |
rs570680644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039878 | CCAGAGGACAGAGGT[A/G]GAACAAGAGTGGCGG | 57690 |
rs570754050 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028107 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT | 57690 |
rs570821017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061217 | AGTTTAATATCAGTA[A/T]TTTAAATGTAAGAAA | 57690 |
rs570823435 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057867 | GGAACGAATGCTACA[G/T]TACAATCATTTTTGT | 57690 |
rs570835224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054475 | TACTGCAGACTACTG[C/T]ACGCCACTGCAGACT | 57690 |
rs570976983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088746 | GCTGTGATTACAGGC[A/G]TGAGCCATCACACCT | 57690 |
rs571007794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081933 | ATATTTGGAGGATGA[A/G]ATCTCTGAAGACTTT | 57690 |
rs571016707 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072391 | TAGAGTTGATGAAGC[A/G]AAAAATGCAGCTCTG | 57690 |
rs571023669 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081188 | TTAGGGTGCTGATCC[A/C]ATTCATGGGGGCTCC | 57690 |
rs571110863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048677 | ACGCTCTTTAAAATG[A/G]GATCTATTAAGAAGA | 57690 |
rs571121394 | in-del | -/AGT | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069509 | TGCCTCAGCCTCCTG[-/AGT]AGTAGCTGGGTCTAC | 57690 |
rs571144604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069854 | TGTGTATGTGAGTGT[C/G]TGTATGCATGCATGC | 57690 |
rs571172297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026896 | TGAGGGTGGAGGGCA[G/T]GTAGGAGCTATTAAT | 57690 |
rs571199901 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054858 | TGCAGACTACTGTAC[A/G]CTACCATACACCACT | 57690 |
rs571211055 | snp | C/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010375 | GAGGTTTTAGAGTCA[C/G]AAAGTATTGGCAGTG | 57690 |
rs571213888 | snp | A/G | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012510 | AAAGGCTTTTTTAAA[A/G]AAGTTCCCTGTTCTC | 57690 |
rs571237078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055056 | ACTGCAGAGTACTGC[A/G]CACCACTGTAGACTG | 57690 |
rs571271996 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041745 | GCATTTATCCTGCCC[C/T]TGAAAACCAAGCAGC | 57690 |
rs571283775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035858 | TGAAAGTATTTTTAG[A/G]TACAGTTTGAAATAA | 57690 |
rs571359705 | snp | C/T | 1.65987e-05 | 0.00288082 | missense | TNRC6C | GRCh38.p7 | 17:78050960 | CTGGTTGGAATGACA[C/T]CACGAGATCTGGGAA | 57690 |
rs571379436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082356 | TTTAACATAACATCG[A/G]TATGCAGAAGTACAG | 57690 |
rs571392748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010963 | AAGGAAGCGGGGCGC[C/T]GTGCTCCGGGGGCGC | 57690 |
rs571430167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096142 | AAAGTAAAGACCTTC[G/T]TGAGGGAATTAACAC | 57690 |
rs571460184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016905 | CCTTGCCCACATGTT[A/G]TGGATGGCATGACTG | 57690 |
rs571478812 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109034 | CATTTTTTATTTTTG[G/T]AGAGATAGGGTCTCA | 57690 |
rs571498019 | snp | C/T | 0 | 0 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071993 | AAGGGATGTCGCCCA[C/T]ATTCGCCATGTATTC | 57690 |
rs571519116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070591 | TTTTCTCTACCCTAT[A/G]AGCTATAAGTAACAA | 57690 |
rs571535147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071419 | TTTCCTAGAATAGAA[A/G]ATGCTTTTTTTTTTT | 57690 |
rs571567947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083793 | TAATTCTTGAAAGTT[C/T]TGTAGCTTCACATAA | 57690 |
rs571611067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043105 | GAAGAACCAAGAAGT[A/G]AGGAACAAGAGAGCA | 57690 |
rs571622277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077575 | GTGTTTGAGCTCTCA[A/G]CACCCTTGGTGCTAA | 57690 |
rs571652627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090111 | TGGGCTTGCAAAGGC[A/G]TTTTGTTAGGTCTGC | 57690 |
rs571718266 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018138 | TGTTTTGTTTTTTTG[G/T]TTTTTTTGAGATGGA | 57690 |
rs571743827 | in-del | -/CTACTGTACATAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030124 | TACTGTACATAATTA[-/CTACTGTACATAA]TGTATGTGCTAGACT | 57690 |
rs571802979 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003611 | GATCAATCCAAGAGA[C/T]TCAATATGTTGTTAT | 57690 |
rs571828341 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024645 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 57690 |
rs571835552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096445 | AATAAAAGTGAAGAC[C/T]TGCAGATTACCCATA | 57690 |
rs571837228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025863 | GAGGAAATCCGTGGA[A/C]TCTGGAATGCTAGCC | 57690 |
rs571841766 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095260 | GCCATGGTGTGAAGA[A/C]GATGGCCCGAGAAAC | 57690 |
rs571875783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78025256 | CACTCCCCTGGCAAC[C/T]GCTGATCTTTTCACC | 57690 |
rs571935925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037799 | TCCAAGTTGCTTTTG[A/G]AACTTGATAGACTAA | 57690 |
rs571945405 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055757 | GGTCTGGCCATGGTT[A/G]GCAGTCATGTATGGA | 57690 |
rs571993480 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105255 | AAAATGAGCCTGTGA[C/T]GATTATGCACATGAC | 57690 |
rs572011808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78090459 | GTACCGTGTGGCGTA[G/T]TACTTACGGTAAGGA | 57690 |
rs572040527 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011748 | TGTTTCATTTTTCAA[G/T]AAATTGCACACAGCT | 57690 |
rs572057507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78044024 | GCTGCAGCAAACATC[A/G]AAGCTCTCTCTTCAA | 57690 |
rs572145233 | snp | A/C | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78051338 | GCAGTACCACGACCA[A/C]TACCACCACCACCAC | 57690 |
rs572202017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019147 | AGTGACTGAGCATGA[C/T]GAGACTCAAGCCAAC | 57690 |
rs572225859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084467 | TTGAGGTCTGCTTTT[A/C]TGTAAGCAGCAGGGG | 57690 |
rs572226860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78072280 | AGCGGCTTCAGTCAT[C/T]CCCTGAGATTACTGT | 57690 |
rs572261213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031102 | TGAGACACTGTCTCA[A/C]ACTTAAAAAAAAAAA | 57690 |
rs572288087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045944 | TGTTATAGGTATCAT[C/T]CTCTAACCCCATTCT | 57690 |
rs572312587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071807 | CAGAGATCACAAAAG[A/T]AAACTTGATGTAAAG | 57690 |
rs572312988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078793 | AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAC | 57690 |
rs572346109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059209 | GTTTTCACATAACTT[C/T]GGAAATAGATCCCAT | 57690 |
rs572361662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005117 | GGGTACATTTATGGC[A/G]GTACCAAAATTTTTA | 57690 |
rs572381955 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013486 | AATCATTTGATCCAG[C/G]AGATATTTATTGAGC | 57690 |
rs572412545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052842 | TCCAGCTAACGCATC[A/G]GTGTCACTAAACCAG | 57690 |
rs572422077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012474 | GTAACAAACCTTCAT[A/G]TGTACCTCCTAACCT | 57690 |
rs572437454 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78058341 | ATTACCTCGCATACT[C/G]AGACATAATATTCTG | 57690 |
rs572460620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074242 | GGACCACAAAAAGGA[C/T]ACTTCTTTACAACCT | 57690 |
rs572501931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104301 | TGTGTACCAGTACGA[C/T]GTTGCCACTAGAAGT | 57690 |
rs572506643 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046043 | GTGTGACATTAAAGT[A/G]CATTTCTTGATTATT | 57690 |
rs572522414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065654 | CTCACAGCAGCCTAA[C/T]GCATCTTGCCGTATT | 57690 |
rs572549529 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088632 | TTTTTTTTCTCTCTC[-/T]TTTTTTTTTTTGGCT | 57690 |
rs572559465 | snp | C/T | 4.96973e-05 | 0.00498459 | missense | TNRC6C | GRCh38.p7 | 17:78079399 | TCCCTGTGCAGATAC[C/T]GAGTGGCAATCTGGG | 57690 |
rs572587548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039050 | ACAGCTCTTTACTGA[C/T]GACTGAATGCTCTGC | 57690 |
rs572641554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006020 | CATGTAGACACATGC[A/G]CTCTCACAGCTAATA | 57690 |
rs572713975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101055 | TGCTGGGATTACAGG[A/C]GTGAGCCACCGTGCC | 57690 |
rs572724328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092488 | TTAAGGGCAGCTTCC[C/T]ATGGTATGGATATGT | 57690 |
rs572788874 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070147 | GAAGTGATTACAGAC[A/G]TCAAAAAGAATCCTT | 57690 |
rs572808772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033617 | GAGGTTGCGGCGAGC[C/T]GAGATCACGCCATTG | 57690 |
rs572831345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079984 | CTTAGAAGCAGCCAA[A/G]GACTGAATCATGCTT | 57690 |
rs572897147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027693 | ATTGTGAGACATATC[C/G]GTATTGCACATACCA | 57690 |
rs572943131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033014 | CAGTTTACAATCAAA[C/T]ATGCTACTTTCCCAA | 57690 |
rs572960903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78014442 | GCGGCATTTTCTAAA[C/T]TGATCTTCTAAATAA | 57690 |
rs572985936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060728 | ATATACTCTTAATTA[A/G]TTACAATTGGCCACC | 57690 |
rs573018637 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085927 | ATATTTGCTGACCAA[-/C]ATCATCACCAACACT | 57690 |
rs573051324 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106916 | GTCCTGCAAGACTGC[A/G]GATCCACAAAAGCTG | 57690 |
rs573114195 | in-del | -/ACC | 0.00653889 | 0.0568039 | cds-indel | TNRC6C | GRCh38.p7 | 17:78051339 | AGTACCACGACCAAT[-/ACC]ACCACCACCACCACC | 57690 |
rs573114519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081503 | AAATGTATTCATTAG[A/G]ATATAGGATAAGCCA | 57690 |
rs573137034 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060561 | CACTGCAACCTCTGC[C/T]TCCCAGGGTCAAGCA | 57690 |
rs573138053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038539 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGCGCC | 57690 |
rs573175989 | in-del | -/CTC | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017614 | GGAGGCTCCAGGCTT[-/CTC]CTAGTGTGGCAGCCA | 57690 |
rs573257077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78041006 | AGGCGGCTCTCGCTG[C/T]ACCCAGCCGACATGT | 57690 |
rs573270825 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087280 | TTTAATTTTAAAAAA[A/T]TTTTTTAATTATTTT | 57690 |
rs573279163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008587 | TTTTCCTCTATGCCT[C/G]TAAGTCTGCAAACCC | 57690 |
rs573280818 | snp | G/T | 0.000399281 | 0.0141238 | missense | TNRC6C | GRCh38.p7 | 17:78049244 | CAGGCTCCAGCTCTG[G/T]CCTGGCTCACTGCTC | 57690 |
rs573293489 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054496 | ACTGCAGACTACTGT[A/C]CACCACTGCAAAGTA | 57690 |
rs573311195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016558 | TTCCAAACTGTTGGA[A/G]ATATGGGAACCAAAT | 57690 |
rs573345645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040340 | TATCTTTAAAAAATA[A/G]TAATAATAATAAGTT | 57690 |
rs573437513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023515 | GTTGAGTCTAGAATA[A/G]AACTTTTGAGCTGGG | 57690 |
rs573446506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78035906 | CTTAAAAGTAATACA[C/T]AGATTTTCATTGTAC | 57690 |
rs573468884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069414 | TTTTTATTTAAAAAA[A/T]TTTTTTTAGAGACAG | 57690 |
rs573501489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78081997 | TTCTTATTCTTTACG[G/T]GCTAACTACTAATGT | 57690 |
rs573510336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068768 | TCGCCTCACTGCACT[C/G]CAGCCTGGGCGACAG | 57690 |
rs573571174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042540 | ATTTCAAAATGGCTG[C/T]TCTTAAAATTCGGTC | 57690 |
rs573571758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009856 | CTGCCCCTGGCCTGA[A/C]TTATGATTTTTAAGT | 57690 |
rs573576551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055559 | TTATATATAATCTTA[C/G]GGGACCATTGTCCTG | 57690 |
rs573592913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102340 | GCATGGGCCTCCCAG[A/G]CTGAGAAAGGCTTTC | 57690 |
rs573598472 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074866 | GGTGTGGCTGCTGCG[A/G]AGAGGATAGAGGGCG | 57690 |
rs573648741 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101791 | TTTGTGGTTTAAGAA[C/T]GCCTTTAAGCAGTCT | 57690 |
rs573678192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109090 | CTGCTGGGAATACAG[A/G]CATGAGCCAGGTGCC | 57690 |
rs573687456 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108577 | CATGGAGGAGGTGGC[A/G]TTTGCCCTGGGCCTG | 57690 |
rs573730723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78070799 | AGTAAAAGTAGTCTA[C/T]ATTTGTGATAAACTA | 57690 |
rs573737791 | snp | C/G/T | 0.000216901 | 0.0104121 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083198 | ATGCAAGTTAGAGCA[C/G/T]GCAGGCCGAGTGCAG | 57690 |
rs573740380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036736 | TAAGACCAGCCTGGC[C/T]AACATAGCGAAACCC | 57690 |
rs573786222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78069961 | CTCTTCGAGAGAACA[A/G]GAACTAAGCAAATGG | 57690 |
rs573799133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082659 | ATCCATATGAACAGG[C/T]GCCCCTCATGCATCC | 57690 |
rs573807153 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074352 | ACAAACAGTGCCCCA[A/G]TTACTGATTTGGGGG | 57690 |
rs573835456 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TNRC6C | GRCh38.p7 | 17:78065393 | TATAAAATATTTGCC[A/G]TGCCTGATACATGAA | 57690 |
rs573871042 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002650 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGTGG | 57690 |
rs573871567 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010427 | TATAAAGTTTAATAT[A/C]AATCAGAATGAAAAG | 57690 |
rs573893100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099498 | GACAAGAAGAGAGAG[A/G]GAGCTTGTGCAGGGA | 57690 |
rs573894386 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084627 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTGAGAC | 57690 |
rs573946726 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054011 | TTACATAAACCTAGA[C/T]GGCATAGCCTCCTGC | 57690 |
rs573957142 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007964 | GCTTTAAATTTGGAT[A/T]TGTTTTAAACATTTT | 57690 |
rs573964794 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089284 | CTTATCTTTACTCTT[A/C]AGGATTTTTTCTCTT | 57690 |
rs573970883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78096184 | ACAGACAGCTCACAC[A/G]TTCCCACTTACAAAC | 57690 |
rs573974822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030928 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57690 |
rs573976716 | in-del | -/GCAAGACC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065333 | AGCCTGAGCAATAGA[-/GCAAGACC]GCAAGACCCCATCTC | 57690 |
rs573999574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064639 | TTATCTTGAAATTAT[G/T]TTGAAATTGAAAACT | 57690 |
rs574003162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024993 | GAGACGGGGTTTCAC[C/G]ATGTTAGCCAGTGTG | 57690 |
rs574005087 | snp | C/T | 3.31796e-05 | 0.00407292 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093797 | CTGCCTCTGCATGGA[C/T]GGTCTCTCTAGACCC | 57690 |
rs574051379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78085035 | CTTTCAGTCCTGCCC[A/G]CCGGAGACCACTGAC | 57690 |
rs574063795 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091431 | TCCTAACCGCATCTC[-/T]CTCTTTAGCTGGACT | 57690 |
rs574079020 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028144 | TTGTGATCTGCCCGC[C/G]TCGGCCTCCCAAAGT | 57690 |
rs574101173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076637 | AATGCACAGGCTGGT[C/T]GTGATGTTAGATGAC | 57690 |
rs574143756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084525 | GTCCCAGAGACACAT[G/T]CTATGTGTCCTCGCT | 57690 |
rs574155645 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051387 | CACCACACACAGGGT[C/T]GAGACGCCGCCCCCG | 57690 |
rs574184229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097156 | GAGGTTGAGGCTGCT[A/G]TGCACTGTGATCATG | 57690 |
rs574243370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78057651 | TGACTACTTCATGAA[A/G]TTTCTGCTATTTTTA | 57690 |
rs574285414 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102864 | TGGGCCTGGCTGGGC[A/G/T]CAGTAGCTCATGCCT | 57690 |
rs574327510 | in-del | -/CTT | 0.00557542 | 0.0525036 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056158 | CCTGGCCAGAAACTA[-/CTT]TTTTTTTTTTTTCTT | 57690 |
rs574335428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78078833 | CGGGGTGGCTCACAC[C/T]TGTAATCCCACCACT | 57690 |
rs574403055 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054224 | CCATGAGTGGAGCTT[A/G]CAGGACTGGAAGTGG | 57690 |
rs574414572 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025795 | CAAAAAAGTATTTCA[C/T]GTCTATATCAAGGCC | 57690 |
rs574438819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78004944 | TGGGCAAAAACTCAT[C/T]TTTAAAATTTTCAAT | 57690 |
rs574491855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080820 | TTTCTTCCCCAAGAG[A/G]CCTCTGATATCAAGA | 57690 |
rs574569889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026991 | CGAGAAAGCTGATGA[A/G]TATATGGGACATGTT | 57690 |
rs574599845 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108295 | TGCTGCTGGCTCTGA[C/G]CATACTCTTTTGGAA | 57690 |
rs574629575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78020169 | TGTCTGTTGCTTTGC[C/T]GAGTGAGGCTTCTCT | 57690 |
rs574665715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78026407 | CCATGTTTTTTGACT[C/T]TGACATTATCAATTG | 57690 |
rs574681301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066416 | GCCACCACTCTGCTC[A/G]AAGTATTCCATTTAT | 57690 |
rs574693934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006723 | GTAACAAATTGCTTA[C/T]TACTGAACAGTGATT | 57690 |
rs574705448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033705 | GTATATATATAAATA[C/T]ACATATAAACACACA | 57690 |
rs574720219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053274 | ATTTCTAGGCCCTTA[C/T]ATTTTATAAAGTACT | 57690 |
rs574720431 | snp | A/G/T | 1.6577e-05 | 0.00287893 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086981 | TCTGCACCCCTCTGC[A/G/T]GGCAAATCGGCCATG | 57690 |
rs574745904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039636 | CTGCCAGTGGTTAAT[G/T]CTGTGGCTGTTGTCA | 57690 |
rs574790130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006122 | GCTGAACAGGAAAGG[A/T]ATTCGTTTACAGATA | 57690 |
rs574816969 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031115 | CACACTTAAAAAAAA[-/AAAG]AAAGAAAGAAATGCA | 57690 |
rs574832536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038885 | ACTCATTTAATCTTC[C/T]CAAGACCCTGTAATC | 57690 |
rs574844191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052877 | CAAAAATCAGTGGTC[C/T]GTGGGCTGCACCTAG | 57690 |
rs574856930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092595 | CTAACTGAAACAGTC[A/G]CTGGCCAGGCATGGT | 57690 |
rs574909625 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105026 | AGTGCGGGCTGCGGT[A/G]GGTCAGCGTCACATG | 57690 |
rs574914803 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031001 | CTACTCTGGAGGCTG[A/G]GGCAGGAAGATCACT | 57690 |
rs574919891 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009466 | AAAGTAGATGTTTTC[A/G]TACAAAAAGCTCAAA | 57690 |
rs574947235 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017594 | TAGAGTTTCTCTCTG[A/C]AACTGGAGGCTCCAG | 57690 |
rs574953169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78059957 | GTGAAATCAAAACTG[A/T]ATAAGATGGTTTTCC | 57690 |
rs575003341 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108681 | GTGTAGGGACCCCAC[A/G]CAAAGACCTCGTGGG | 57690 |
rs575023373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080172 | AAAAATGTTGCCGGG[C/T]GCGGCGGCTCACGCC | 57690 |
rs575023482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78034299 | TGACCTCAGGTGATC[C/T]GCCTGCCTCAGCCTC | 57690 |
rs575031206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046817 | AACAGCATTTATTAG[C/T]CACCAGCTTATAATG | 57690 |
rs575042436 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106277 | AAAAAGACTTCCGTC[A/G]TAAAGAAACCTATTT | 57690 |
rs575140776 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78022349 | ATTCCATATCCAAAT[A/G]TCTTAGAATTTGGTG | 57690 |
rs575218873 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015686 | GGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC | 57690 |
rs575230749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074666 | GATACAGGACTCGGT[A/G]AATGGAGAGGCATGG | 57690 |
rs575256844 | in-del | -/GT | 0.196064 | 0.244113 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105636 | TGTTGAAACAGAAGT[-/GT]GTGTGTGTGTGTGCA | 57690 |
rs575283237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082075 | GACAAATATAATTAT[C/T]ATTGCAGGATCTGGC | 57690 |
rs575287247 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034024 | AGCCGAGTCTCCCCA[A/G]CATTTTCCCCGCCTA | 57690 |
rs575318246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78088369 | TGGGCAACTTGCCTA[C/G]CTGCTGTTTGCTTCA | 57690 |
rs575319001 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035446 | TATAGTAGGTGTTGA[A/G]TAATGCAGGTGATAG | 57690 |
rs575322423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78048405 | CCATGTTTCGCCTCT[A/G]TATAATACTGTAACC | 57690 |
rs575367156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094719 | TGCTGGGATTACAGG[C/T]GTGAGCCAGTGTGCC | 57690 |
rs575369378 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004334 | TTTGCATCATCATAG[C/T]CATTATATGACAAGG | 57690 |
rs575403882 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101626 | ACAGAGATTTACCCA[C/T]GTATTTATTAACAGC | 57690 |
rs575413468 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054622 | GACTACTGTAGACTA[C/G]TATACACCACTGCAG | 57690 |
rs575449329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109159 | ACATCACGGCAGAAC[A/G]GTAAAGGCAGAAAGC | 57690 |
rs575462041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009662 | CAGGTTCAAGCAATT[C/T]TGCTGCCTCAGCCTC | 57690 |
rs575465739 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094091 | TTCAAGCGACTCTCC[C/T]GCCTCAGCCTCCCAA | 57690 |
rs575510739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075394 | TATAATACTTAAGTG[A/G]CTTTTATCCATTTTT | 57690 |
rs575607127 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003470 | AGCACAAGAAGGTTA[A/G]CAATTTTAAACATCA | 57690 |
rs575614253 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080102 | GCCAATAGAGTTGGG[-/T]TTTTTTTCTTTCTTT | 57690 |
rs575679084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78099731 | AATCTCATGTCCTCA[C/T]ATTTCAAAACCAATC | 57690 |
rs575722410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102674 | GTCCATAAGTGACGC[C/T]GCATGGGAGGAGATG | 57690 |
rs575730786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010657 | CTAAGAAATTGATTG[G/T]ATGAGGTATCTTTAG | 57690 |
rs575763507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102435 | GCACTATCCACTGGC[A/G]CGGGGCCTTGTCAAC | 57690 |
rs575785393 | snp | A/C | | | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064825 | TAATGGCACAGCAGC[A/C]TGGGGGAAGCCACCC | 57690 |
rs575796535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024313 | GTGGGTTGTATTTCC[A/G]TTTTTTATTAATAGG | 57690 |
rs575862232 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079827 | TATTGAGGGGGAAGG[A/T]CCTGCCCAACACACT | 57690 |
rs575887420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78037344 | ATGCCTACCAAACAT[C/T]ACATACCCTGCACTG | 57690 |
rs575895157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063116 | CCGAGCATGTTGTTG[C/T]GTGCCTGTAGTCCCA | 57690 |
rs575956908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78089845 | AAAGGGGAAGCCTCA[C/T]GTAGCACAGAAGAAA | 57690 |
rs576159952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78031023 | AAGATCACTTGAATC[C/T]GGGAGGTGGAGGTTG | 57690 |
rs576170970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056454 | TGAACCACCATGGCC[A/G]GCCCAGAAACTACTT | 57690 |
rs576205318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055597 | TCAGTTGACCAAACC[C/G]TCATTATGCAGCCCA | 57690 |
rs576207668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78052741 | GCCCTCCAGCCTCCT[C/T]GTAGACTTCTTGGTG | 57690 |
rs576208024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043940 | CATTGTGTATATCTG[C/G]CATATTTTCTTTATT | 57690 |
rs576255796 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077766 | GAAATAAAGATGACA[G/T]CTCTTGCAAGGTGGT | 57690 |
rs576323607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78019108 | AAGGTCGGGGGCCTC[A/G]GCTGTTACAGATGAC | 57690 |
rs576324678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78043379 | GGTTCCTTCTTAAGT[A/G]AAATAGCATTGTTCC | 57690 |
rs576344511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78084006 | GACCAGGAATCGGCC[A/G]GGCACGGTGGCTCAT | 57690 |
rs576347668 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010961 | GCAAGGAAGCGGGGC[A/G]CTGTGCTCCGGGGGC | 57690 |
rs576350029 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100338 | CCCACAGCAAAGTAT[C/T]GTCTGAACATCCAGG | 57690 |
rs576367639 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043387 | CTTAAGTAAAATAGC[A/G]TTGTTCCAAATTGAC | 57690 |
rs576371195 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059556 | GAAGACAGTTGAAAA[C/T]ACAGTGTGAGGCCGG | 57690 |
rs576381095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079860 | CATTGATGTGCTTTT[G/T]TCCCAGTCTTTGTCG | 57690 |
rs576388117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018416 | TTATAGGCGTGAGCC[A/T]CCATGCCCAGCCGGA | 57690 |
rs576403022 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039118 | CAAGTTGGAACGTGT[C/T]GAGAGGCAGTAGGGA | 57690 |
rs576463906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011941 | GCTTATTTGTCATCT[G/T]GGTGAAGCGTCTTTT | 57690 |
rs576467394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079208 | GAGCCAAGACCGCGC[C/T]ACTGCACTCCAGTCT | 57690 |
rs576478481 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068479 | CCAAAAAGTTTGAGA[C/G]AGATGGTTAAGAAGT | 57690 |
rs576518511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103641 | GCAGGGGTGTCCTGA[A/G]CCACCATAGCAGAAT | 57690 |
rs576529339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091744 | ATAACCCATTCCATT[A/G]TAGTGCATATAAGAT | 57690 |
rs576745824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005037 | TTCTTTCTTTCTTTC[C/T]CTCTCTTTTTTTTTT | 57690 |
rs576764194 | in-del | -/AACT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096767 | TCCTGTGTTCACCCC[-/AACT]GTCACCATTATTCCA | 57690 |
rs576819094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038934 | GAGTGTGGGAAAAGG[C/T]GACGCTGGTGTGCTG | 57690 |
rs576850988 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005870 | TTCAAAATAAAATGT[-/A]AAAAAAAAAGACTAA | 57690 |
rs576904279 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNRC6C | GRCh38.p7 | 17:78045318 | AACAGGCATGACTTC[A/C]TCCTTATGGCATCCT | 57690 |
rs576912713 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78038509 | AAACCCCATCTCTAC[A/T]AAAAAAAAAAATACA | 57690 |
rs576922549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78006870 | TGCTCTATCGCCCAG[C/G]CTGGGTGGAGTACAG | 57690 |
rs576989584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067011 | ATTCGCGTGGTTCCT[A/G]TGCAAGGATGAGATA | 57690 |
rs577032048 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | TNRC6C | GRCh38.p7 | 17:78053091 | ATACCATGTCACGTT[-/G]GCCCCCCGACCCCTG | 57690 |
rs577032292 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085406 | ATAAGGATTCACTTA[A/G]GTGGGGTATTTTATT | 57690 |
rs577040132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028179 | GGATTACAGGCGTGA[A/G]CCATCGCCCCCCGCT | 57690 |
rs577076210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073697 | TTGGGTTCCTATGAG[C/T]CTCTGCTCACAACAT | 57690 |
rs577081871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78066489 | GTATTTAGATTCATG[C/T]GCCATTTTGAGCATT | 57690 |
rs577111369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060019 | GGCAGGCAGAAGAAG[C/G]TGTTCTAAGGGAAGT | 57690 |
rs577154002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78046996 | TATTCGAATGGCACC[C/T]CACATATGGAAAAGA | 57690 |
rs577168513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093294 | CAGATCAATTTTGGG[A/T]ATGGTTAGCATCAGG | 57690 |
rs577201415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027661 | TGCCCCCTTGCATTG[C/T]CTCTCTGACCCCATT | 57690 |
rs577215574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78054694 | CTACTGCAGACTACT[A/G]TAGACTACTATACAC | 57690 |
rs577223752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78023372 | CACAAAAATTTCTGT[A/G]GCTTGCTAATAGTTC | 57690 |
rs577240778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78033596 | ATCGCTTGAACCTGG[A/G]ACGTGGAGGTTGCGG | 57690 |
rs577241021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78027067 | AAAAGAACAGGAAAC[C/T]TGCCAAGGGGGATGG | 57690 |
rs577241167 | in-del | -/CC | 0.00199481 | 0.0315187 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077736 | AAAGCACCACATTCT[-/CC]CCCCCTTTTTCCCAG | 57690 |
rs577278105 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78018129 | TTGGTTTTTGTTTTG[-/T]TTTTTTTGGTTTTTT | 57690 |
rs577286221 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020834 | CAATTTAGACCTCAA[A/G]GCTCAATAGCCACAC | 57690 |
rs577344972 | in-del | -/A | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106884 | AAACAAAAAAAATAC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs577348454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78028733 | TTTTTAATGTTTCTT[C/T]TACATAAAAGGTATG | 57690 |
rs577427021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78060628 | CTACAGGTGTGTGCC[A/G]CCATGTTGGCTAGGC | 57690 |
rs577441600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087664 | GTTTGGTCAGTAAAA[A/G]TATTCAGATTTACAT | 57690 |
rs577513717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040307 | GGATAGCTCCAGCTT[C/G]AAACACTTGAGAGCT | 57690 |
rs577525540 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78055017 | CTGTACACCACTGCA[A/C/T]AGTAGAGTTCAGCAC | 57690 |
rs577533306 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015844 | TGGAACCCAGGAAGC[A/G]GAGGTTGCAGTAAGC | 57690 |
rs577553081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074411 | TACAAGTACAGAATT[C/G]ATGAATAATGAGGAT | 57690 |
rs577570863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78076580 | GTTTATTTGCTAATC[C/T]GGCAACCCTAAATTG | 57690 |
rs577572331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78015367 | CCAAATTTCAGAAAG[A/G]AGATGTGTTAAAATG | 57690 |
rs577587341 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005570 | TGTTGGTGGAAACAC[A/G]CGCATTTCTCACTGT | 57690 |
rs577593309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78080937 | ATTTAATTTAAATGT[A/G]TTTAGTTTGTTGGAA | 57690 |
rs577600355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78061543 | AATACTGGGCCAGGT[A/G]TGGGGGCAGGCATCT | 57690 |
rs577663516 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088128 | CTATTCAATGTCTCT[C/G]AAAAGAGCGGTATAT | 57690 |
rs577670427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008724 | CTTTTTCTTATTTTT[C/T]CCTCCTGTGATGAAA | 57690 |
rs577679392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78068716 | AGAGAATTGCTTAAA[C/T]CTGGGAGGCGGAGGT | 57690 |
rs577684380 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007222 | TCCTCTAAAATACTG[-/T]TCCTTTGGGTACAGT | 57690 |
rs577804117 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78074290 | CTGAACTGGGAACTT[-/G]GGCAACTCACATTTT | 57690 |
rs577884043 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002510 | TGCTGTTGTAATAGC[A/G]ATAATTTGTTTTACT | 57690 |
rs577896661 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087594 | TAGTCTACTCTGAAC[C/T]GTACTTTACCAGCCA | 57690 |
rs577990670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78094802 | TTGGCTGGAAAGCCA[A/G]CATAAGTACAGATTG | 57690 |
rs578019765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78101715 | GGAGATAAAGGGATG[C/G]GTTTGGCTAGTTATC | 57690 |
rs578070141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78036224 | GTACGTAAACTCTTT[A/G]TGCCCTCCCCCCAGG | 57690 |
rs578084324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78042468 | GTATGGAAATACTTC[A/G]AACTCCGAAATGGTA | 57690 |
rs578086232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030091 | CCAGTAATATAGTTA[A/T]TATGAACCATTATGT | 57690 |
rs578090630 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011306 | TCATCCCTGAAGGTG[G/T]CCTTGTGACCTTTTC | 57690 |
rs578094445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78005289 | ATCTAAAAATGTCTG[A/G]AGAATGTTATATTAG | 57690 |
rs578128820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78017409 | TTCCTGCTCAGGTGG[C/T]GGAGCTGAACAAGGA | 57690 |
rs578176577 | in-del | -/C | 0.0209421 | 0.100162 | intron-variant | TNRC6C | GRCh38.p7 | 17:78056551 | TCACTGCAAGCTCCG[-/C]CTCCCAGGTTCACGC | 57690 |
rs578183360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78016753 | TGCTTCTGAGAGGAG[G/T]AGGATTATTATACTA | 57690 |
rs578203237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNRC6C | GRCh38.p7 | 17:78063170 | AGAACCCCTTAACCC[A/G]GGAGGCGGTGGTTGC | 57690 |
rs578213962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109225 | AAGGCTGTTCCAATG[C/G]GGGAGAAGCCAGCAG | 57690 |
rs578248835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNRC6C | GRCh38.p7 | 17:78024942 | GGGATTACAGGTGTG[C/T]GCCATGACGCCCAGC | 57690 |
rs578258331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNRC6C | GRCh38.p7 | 17:78030485 | CATCACCACAAACAC[A/G]TGAGTAATGTGTTGT | 57690 |
rs745313659 | snp | C/T | 1.89141e-05 | 0.00307518 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077380 | CCTTTGTTTTACCTG[C/T]CTTCTAAAAAATGTG | 57690 |
rs745330217 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016686 | TCCCTTCTTTAGGTC[A/G]TTCTCTGTGGTTCCT | 57690 |
rs745343753 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090877 | TAGAACTGAATTATC[C/T]TATCAGTCTGTTTCA | 57690 |
rs745368631 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059722 | GGCATAGTGGCACAC[A/G]CCTCTAGTCCCGGCT | 57690 |
rs745383698 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027095 | TGGGAAATAGTGGCA[A/T]AGAGAAGAAGGCAGG | 57690 |
rs745416812 | snp | C/T | 1.65748e-05 | 0.00287874 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049629 | AAATAACACTAACCC[C/T]ATGAACTCTTCACCC | 57690 |
rs745418876 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071635 | TCAAGCGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 57690 |
rs745423738 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058520 | AGATTTCACTGAAAT[A/G]TAGATAATTTTAGAG | 57690 |
rs745436996 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100570 | GCACACAGCATGTGG[A/T]CCCTGGGCCTGGCCC | 57690 |
rs745484389 | snp | G/T | 1.68233e-05 | 0.00290023 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087133 | GCCACATCAGGTAGA[G/T]AGGGTACCTGGAGTC | 57690 |
rs745484905 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083395 | TTGTTTAGAGGCAGC[A/G]TCTTACTATGTTGCC | 57690 |
rs745485469 | snp | A/G | 1.70316e-05 | 0.00291813 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098547 | CCTCGGGTAAGCTCC[A/G]TGCTCCTCGTGTTCC | 57690 |
rs745546410 | snp | A/G | 1.77344e-05 | 0.00297773 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067964 | TACACCCTGAAAACC[A/G]AAGGTACTTCAGACA | 57690 |
rs745570399 | snp | A/T | 1.65767e-05 | 0.00287891 | missense | TNRC6C | GRCh38.p7 | 17:78098453 | AGTACTGCACCCACG[A/T]GGCCACCTCCAGGGT | 57690 |
rs745575120 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025989 | AACCTTTCATTTCCA[C/G]ATGAGAAAACTGAGG | 57690 |
rs745610134 | snp | A/G | 1.65638e-05 | 0.00287778 | missense | TNRC6C | GRCh38.p7 | 17:78093724 | CCTACCATCAACACC[A/G]CCATCCAGGATGTCA | 57690 |
rs745649647 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022467 | GTTTTGAAGAAAAAC[A/C]ACCCTGAATTTGTCC | 57690 |
rs745650988 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066470 | AGGATAAGGGAACTT[A/G]TGAGTATTTAGATTC | 57690 |
rs745688954 | snp | C/T | 1.65814e-05 | 0.00287931 | missense | TNRC6C | GRCh38.p7 | 17:78049496 | AGAACGGGAACCCAA[C/T]AGGCACTTTAGGTGC | 57690 |
rs745704147 | snp | A/G | 1.92469e-05 | 0.00310211 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064895 | CCGGTGGCATTTGGA[A/G]GAGCTGGCGCACCTG | 57690 |
rs745705093 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034635 | TGCTGATTAGGTCAT[A/G]AGAGTCTTGCCTTTA | 57690 |
rs745716049 | snp | A/C | 1.8182e-05 | 0.00301507 | missense | TNRC6C | GRCh38.p7 | 17:78050277 | TGATGGTTCTGGCAA[A/C]CACAATGAAGGAAGC | 57690 |
rs745740159 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047837 | ATTTTTTAGTGATAC[A/G]TACTTGGAATAAAGT | 57690 |
rs745770217 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090777 | GCACCCCCGCTGTCA[A/G]ATAGTTCAGTTCCTT | 57690 |
rs745819422 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | TNRC6C | GRCh38.p7 | 17:78079452 | GCACAAGCCAGGACC[A/G]TGCAGCAGCCGCCAC | 57690 |
rs745831401 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101754 | GAGCATATCCTTAAG[A/G]CACAGATCGCTCGTG | 57690 |
rs745847929 | snp | C/G | 1.73573e-05 | 0.00294591 | missense | TNRC6C | GRCh38.p7 | 17:78049713 | TGGTATGGGGGCCAT[C/G]ATCCCGCCCCACCTG | 57690 |
rs745863044 | in-del | -/TT | 1.65902e-05 | 0.00288008 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079373 | TGCCTTGGTAACGTG[-/TT]TTTAATTCTGTCCCT | 57690 |
rs745863944 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004340 | TCATCATAGCCATTA[C/T]ATGACAAGGTTTCAT | 57690 |
rs745871209 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067264 | GGCAGGAGGATCACT[G/T]GAGCCCAGGAGTTTG | 57690 |
rs745875506 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017600 | TTCTCTCTGAAACTG[G/T]AGGCTCCAGGCTTCT | 57690 |
rs745883859 | snp | C/G | 3.24807e-05 | 0.0040298 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78102535 | CGTTCTTCGAAACCT[C/G]ACTCCCCAGGTGCAA | 57690 |
rs745938423 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102419 | AGAAGTGGGGAGGGC[C/T]GCACTATCCACTGGC | 57690 |
rs745954785 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041880 | GTGATGATAAAGAAT[A/G]AACACATTTACTATT | 57690 |
rs745987513 | snp | G/T | 2.62595e-05 | 0.0036234 | missense | TNRC6C | GRCh38.p7 | 17:78075204 | GACCATAATGGAATG[G/T]CCGCCAAGCCCCTCG | 57690 |
rs746011968 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097874 | CAGGTACGCGCCTGG[A/C]CTCTAGACTTGCAGG | 57690 |
rs746027669 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067302 | AGTGAGCTGTGATTG[C/T]ACTACTATAATCCGG | 57690 |
rs746051681 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068420 | TGTCAACAGAAGTTC[-/T]TTGGGATCTTCAGTC | 57690 |
rs746065102 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097071 | AAGGGAATCATGAGC[C/T]GGGTGTGGTGGCATG | 57690 |
rs746072584 | in-del | -/TAGC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056592 | CCTCAGCCTCCCGAG[-/TAGC]TAGGACTACAGGTGC | 57690 |
rs746097034 | snp | C/T | 1.66034e-05 | 0.00288122 | missense | TNRC6C | GRCh38.p7 | 17:78086956 | CGCCACCGCCCCCGC[C/T]GCACCTGTCTCTGCA | 57690 |
rs746100440 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108885 | GGTCTCTGTCTCCCA[C/T]GCTGGAGTGCAGTGA | 57690 |
rs746115714 | snp | C/T | 0.000130608 | 0.00808003 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097700 | TTAGAGTCATGAACC[C/T]GGACACCGCCACCAC | 57690 |
rs746122613 | snp | A/G | 1.72591e-05 | 0.00293756 | missense | TNRC6C | GRCh38.p7 | 17:78050351 | GGATTATAGACCAAG[A/G]GCACATCCAGTTGCC | 57690 |
rs746127983 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068409 | GACACAACTCATGTC[A/G]ACAGAAGTTCTTTGG | 57690 |
rs746157001 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059460 | GATGCTTCTCAGTGC[A/G]AGTCCGTGGCGTGAG | 57690 |
rs746170897 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029381 | CTCTACAGCATGTTA[A/C]TATACTGAATACTGT | 57690 |
rs746181600 | snp | G/T | 1.66007e-05 | 0.00288098 | missense | TNRC6C | GRCh38.p7 | 17:78083132 | TTAATCCTCAACATA[G/T]GACGATGTTGAACCA | 57690 |
rs746182544 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019870 | AGAAGGGGAATGTCA[A/G]GATTGCTTTGATGCC | 57690 |
rs746235847 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018605 | TGAGCCCTTATTTAC[C/T]GTGCTTTCCTTTTTT | 57690 |
rs746242295 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063830 | AAGAATAATATTTCA[A/G]TATATATTTGCAACT | 57690 |
rs746274292 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092660 | CAAGGTGGGAGGATC[A/G]CTTGAGCCCAGGAGG | 57690 |
rs746341081 | snp | A/G | 1.76191e-05 | 0.00296804 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092920 | GCTTCTTTGTTTCCT[A/G]TTGTCCCCATAGGTG | 57690 |
rs746397787 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073731 | TGTCAACCAATCAAT[A/T]TATAACCTTGTTTTA | 57690 |
rs746403338 | snp | A/C | 3.86406e-05 | 0.00439532 | missense | TNRC6C | GRCh38.p7 | 17:78051034 | ACAAACTGGGGGGAG[A/C]CTTTAAAACCTGGCC | 57690 |
rs746431810 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030227 | CAGTCTCGGCTCACT[A/G]CAACCTCCACCTCCC | 57690 |
rs746448940 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074800 | AAACTAGGGGAGGGG[G/T]TGCATCCCAGGGGAG | 57690 |
rs746449439 | snp | A/G | 0.000492975 | 0.0156922 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104868 | CATCATCAGCACCAG[A/G]AGAGCCGACCCCTCC | 57690 |
rs746459283 | snp | A/G | 1.65704e-05 | 0.00287836 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064811 | TCTACCCTGGTGGAT[A/G]ATGGCACAGCAGCAT | 57690 |
rs746461765 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068639 | TCTCTACTAAAAATA[C/T]AAAAACTAGCTGGGC | 57690 |
rs746501332 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056993 | GTTCTCCCCTGCAAC[C/T]TTTGCAGCCTGTGCA | 57690 |
rs746540426 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038909 | TGTAATCACCGCAGG[C/T]GACCAGCGAGAGTGT | 57690 |
rs746549541 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038440 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 57690 |
rs746613578 | snp | C/T | 2.05844e-05 | 0.00320808 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091567 | CATGGATAACTTGCC[C/T]AGTGCCGCTTCCCCC | 57690 |
rs746632610 | snp | A/C | 1.65597e-05 | 0.00287743 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079466 | CATGCAGCAGCCGCC[A/C]CAGCCACCAGTGCAG | 57690 |
rs746686290 | snp | A/C | 1.66219e-05 | 0.00288283 | missense | TNRC6C | GRCh38.p7 | 17:78050885 | CGTCTGTCCTTGGAC[A/C]CTTGGGGGATGGGAA | 57690 |
rs746686503 | snp | C/T | 3.31746e-05 | 0.00407262 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049635 | CACTAACCCCATGAA[C/T]TCTTCACCCAACCCT | 57690 |
rs746712418 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008799 | AAAGAGAAATTAAAG[C/T]TCACTCGAAATTCCT | 57690 |
rs746729729 | snp | C/G | 4.97731e-05 | 0.00498839 | missense | TNRC6C | GRCh38.p7 | 17:78086965 | CCCCGCCGCACCTGT[C/G]TCTGCACCCCTCTGC | 57690 |
rs746738517 | in-del | -/GTT | 1.67699e-05 | 0.00289563 | splice-donor-variant | TNRC6C | GRCh38.p7 | 17:78086586 | CAACAGGAGCAGCAA[-/GTT]GTAGGTGCTACCCAG | 57690 |
rs746746351 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047483 | TTACATTACTCTTAA[A/C]TCAGGCAATAAAAAT | 57690 |
rs746824519 | snp | A/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002840 | ATAAATAGCACATGT[A/T]AGTTGTATAGTTCTT | 57690 |
rs746831142 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016608 | CCAGAGTAAGATCTA[A/G]TCCTCCATTCCTGAG | 57690 |
rs746839347 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046067 | GATTATTAATGAGGT[G/T]GATTATTGTTTCATA | 57690 |
rs746873316 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058402 | AAGAGAACATTGAAT[A/G]TTAATTAACAAAACC | 57690 |
rs746874665 | in-del | -/CTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075346 | CATTTCAACTGTGTC[-/CTT]AATACAAGCCAGATT | 57690 |
rs746915346 | snp | A/G | 0.000502828 | 0.0158481 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097708 | ATGAACCCGGACACC[A/G]CCACCACCTTGCTCA | 57690 |
rs746953097 | snp | A/G | 3.982e-05 | 0.00446189 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064902 | CATTTGGAAGAGCTG[A/G]CGCACCTGTTGCTGC | 57690 |
rs746983667 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015770 | TACAAAAATTAGCTG[C/G]GCGTGGTGGTGGGCG | 57690 |
rs747002962 | snp | C/T | 1.6566e-05 | 0.00287797 | missense | TNRC6C | GRCh38.p7 | 17:78093742 | ATCCAGGATGTCAAC[C/T]GCTACCTCCTCAAGA | 57690 |
rs747030026 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026983 | GGGCGAGGCGAGAAA[G/T]CTGATGAGTATATGG | 57690 |
rs747033545 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005088 | ACCAAAGGTAAGTTT[A/G]TTTATATTTAGGGGG | 57690 |
rs747049105 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100758 | GAATTTTTCCTCAGA[A/C]AATGGGATTTCCTTT | 57690 |
rs747066911 | snp | C/T | 1.66635e-05 | 0.00288643 | missense | TNRC6C | GRCh38.p7 | 17:78092962 | GGTCTAAGCATTGGG[C/T]CTCCAGGTAAGTCCT | 57690 |
rs747094756 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022318 | TGCATCAGGCAGGTA[A/G]CACACAGGAAACCAT | 57690 |
rs747103630 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054767 | CTGTGGACTACTGTA[C/G]ACTACTATACATTAC | 57690 |
rs747110193 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053808 | AGGCTGAGGTGGAAG[C/G]ATGGCTTGAGCCCAG | 57690 |
rs747122913 | snp | C/T | 3.35616e-05 | 0.0040963 | missense | TNRC6C | GRCh38.p7 | 17:78051209 | AAGAACCCTCTCCAC[C/T]GTCCATTCGCCGCAA | 57690 |
rs747155226 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065251 | CAGCTATTCGGGAGG[C/G]TATGGTGGGAGAATT | 57690 |
rs747171159 | in-del | -/A/AAA | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106522 | CTGAAGATGTTATTT[-/A/AAA]AAAAAAAAAAAAAAC | 57690 |
rs747190842 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079035 | GGTAGAGGTTGCAGT[A/G]AGCTGAGATCGCACT | 57690 |
rs747216762 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107280 | TTGTTTGTTTTTTGT[A/T]TTTTTTACCTTTTAT | 57690 |
rs747226511 | snp | A/G | 1.6633e-05 | 0.00288378 | missense | TNRC6C | GRCh38.p7 | 17:78049384 | AATGCCAACCCAGCT[A/G]CCTGGCCTGTACTTG | 57690 |
rs747232180 | snp | C/T | 1.66172e-05 | 0.00288242 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103579 | TCACAGCCACCTCAG[C/T]GCTCCAAGTAGCTCC | 57690 |
rs747233195 | snp | C/G | 7.27599e-05 | 0.00603114 | missense | TNRC6C | GRCh38.p7 | 17:78051069 | ACAGAACTGGGCTAG[C/G]AAACCCCAAGACAAC | 57690 |
rs747244285 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078144 | ACTCACCAGCGCCCG[A/T]CTGTGTGATCCTGGC | 57690 |
rs747251819 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098647 | CCTGTAACTCTGGAG[C/G]CTGGGAGGGCTTAGG | 57690 |
rs747269969 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106145 | GAAACAAGCACTTGG[C/G]CGTGGGTTGTGACTG | 57690 |
rs747287200 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020997 | CACTTAAGTGAGAAA[C/T]CTAAGTGCTCCAGTG | 57690 |
rs747310762 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052480 | CTAGTGAGGGTGGCA[A/G]ACAACACACGAATTA | 57690 |
rs747314649 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018020 | AATGTGTAATTTTCT[A/G]TTTGTGAAATCATTT | 57690 |
rs747369721 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073608 | CTTATTTTCTTGGTA[C/G]TTATGTTCTATAAAG | 57690 |
rs747405087 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042985 | CCTAAGCCTACCCTT[C/T]AAAAAAGAGCTTATA | 57690 |
rs747411320 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028807 | AGCTATCAAACCAGT[A/G]ATGTTTACAAATTGA | 57690 |
rs747417890 | snp | C/T | 1.67044e-05 | 0.00288997 | missense | TNRC6C | GRCh38.p7 | 17:78067889 | CCTCCTCCTGCAGCT[C/T]CTGGGGGAACGCCCC | 57690 |
rs747419686 | snp | C/G | 1.71446e-05 | 0.0029278 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086620 | GATTTTTGTCATGAG[C/G]TATAATTTTCCCTGA | 57690 |
rs747422629 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085038 | TCAGTCCTGCCCGCC[A/G]GAGACCACTGACCTC | 57690 |
rs747453364 | snp | C/T | 1.71894e-05 | 0.00293162 | missense | TNRC6C | GRCh38.p7 | 17:78050069 | CCAGCCGAAGCACCT[C/T]TAACGGTGTGAATGG | 57690 |
rs747465200 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072226 | GACGGTGGCTTCAGC[A/G]TGTCCTGATTTATAC | 57690 |
rs747480228 | snp | A/C | 1.65963e-05 | 0.0028806 | missense | TNRC6C | GRCh38.p7 | 17:78093060 | AGCTGTTCCCCATAG[A/C]TGGTCACGTGCCAAA | 57690 |
rs747501607 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079343 | CCCTACCTCCAAACA[A/G]TGTTACTCTAATGCC | 57690 |
rs747506258 | snp | G/T | 1.823e-05 | 0.00301905 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086481 | ATTATCATACTATTT[G/T]AACTCTTCGTTCTGT | 57690 |
rs747519642 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096768 | CCTGTGTTCACCCCA[A/G]CTGTCACCATTATTC | 57690 |
rs747521336 | in-del | -/AGG | 0.0001335 | 0.00816898 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050529 | TCAGGCTTCAAACTC[-/AGG]GGGGAAGAACGATGG | 57690 |
rs747526409 | snp | A/C | 1.66034e-05 | 0.00288122 | missense | TNRC6C | GRCh38.p7 | 17:78083144 | ATATGACGATGTTGA[A/C]CCAGCTCTATCAGCT | 57690 |
rs747547755 | snp | A/C | 7.53097e-05 | 0.00613589 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097775 | CATCTCAGAATGCCA[A/C]GCTGCCTTCTTCGAG | 57690 |
rs747552448 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083816 | TCACATAATCTTGAT[A/T]TTTTTTTAATTTTCA | 57690 |
rs747553173 | snp | C/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012573 | ATAAGCAAATATATG[C/T]ATATGCAAATGAATG | 57690 |
rs747569998 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008552 | CTTTCATCAGTTTCT[G/T]CCTCTTGACTCCCCC | 57690 |
rs747582474 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037573 | AAGGTGAAAGGGCGT[C/T]GCAGATGGAGTGACC | 57690 |
rs747679067 | in-del | -/GTT | | | cds-indel | TNRC6C | GRCh38.p7 | 17:78105780 | CGCATTGGTCAAACG[-/GTT]GTTATTATTAGCTTC | 57690 |
rs747682171 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051225 | GTCCATTCGCCGCAA[A/G]ATGGAAATTGATGAT | 57690 |
rs747707305 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007228 | AAAATACTGTTCCTT[C/T]GGGTACAGTTTATCA | 57690 |
rs747719726 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036552 | AGTGGAATTTGTAGC[A/G]TTTTTAGCTGTGTAA | 57690 |
rs747751626 | snp | C/G | 1.65932e-05 | 0.00288034 | missense | TNRC6C | GRCh38.p7 | 17:78083113 | GCACTATTAACCTCG[C/G]CAATTAATCCTCAAC | 57690 |
rs747770086 | snp | C/G/T | 3.80693e-05 | 0.00436274 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092904 | TGGAGAGTATTCACT[C/G/T]GCTTCTTTGTTTCCT | 57690 |
rs747776425 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092449 | TAATCACAAAGACTC[A/G]TAAGTTGTCCCCAAA | 57690 |
rs747788564 | snp | C/T | 4.61936e-05 | 0.00480569 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064923 | CTGTTGCTGCCTCAG[C/T]CCTGTGCAAACCAGG | 57690 |
rs747812695 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039954 | TTATTCCTTCCCCCT[C/T]CACTGGCAGTAGCCA | 57690 |
rs747816017 | in-del | -/CCACCA | 1.66743e-05 | 0.00288736 | cds-indel | TNRC6C | GRCh38.p7 | 17:78086934 | CTGCTCGTGAAGCAG[-/CCACCA]CCGCCACCGCCCCCG | 57690 |
rs747824040 | in-del | -/CTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013985 | ATAAGGCCAATTTCT[-/CTC]CTCCTGCACCAGCCT | 57690 |
rs747832750 | snp | A/C | 0.00624701 | 0.0555381 | missense | TNRC6C | GRCh38.p7 | 17:78049826 | GACTGTCCCCAGGTA[A/C]CCCTGCCACAGGAAA | 57690 |
rs747877528 | in-del | -/AAAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092741 | TTGTCTCAAAAAAAT[-/AAAT]AAATAAATAAATAAA | 57690 |
rs747896023 | snp | A/G | 3.55954e-05 | 0.00421858 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077144 | GTGCTTTGTCTGCTG[A/G]TGGACACTGCACACA | 57690 |
rs747954361 | snp | G/T | 3.31763e-05 | 0.00407272 | missense | TNRC6C | GRCh38.p7 | 17:78049487 | TGGGCAACCAGAACG[G/T]GAACCCAACAGGCAC | 57690 |
rs747990614 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099046 | ATTGCAGCTTCTCTC[A/G]GGTGCTGCATGTCGA | 57690 |
rs748049263 | snp | A/C | 3.32657e-05 | 0.0040782 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049395 | AGCTGCCTGGCCTGT[A/C]CTTGGACATGAAGGA | 57690 |
rs748049870 | snp | C/T | 1.65734e-05 | 0.00287862 | missense | TNRC6C | GRCh38.p7 | 17:78087075 | TCTTCACCCAACACC[C/T]TTGCTCCTTACCCTC | 57690 |
rs748058302 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098065 | GCACATGGAAGTGGT[A/G]ACGTCTTCTCCATAC | 57690 |
rs748094940 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024869 | GTGCGATCTCAGCTC[A/G]CTGCAGCCTCTGCCT | 57690 |
rs748106171 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081394 | TAATTGTTCAAACCC[A/G]GGTTTGTGCACTGAG | 57690 |
rs748118163 | snp | A/G | 3.34661e-05 | 0.00409047 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050535 | TTCAAACTCAGGGGG[A/G]AAGAACGATGGGTCC | 57690 |
rs748143925 | snp | C/T | 1.65781e-05 | 0.00287902 | missense | TNRC6C | GRCh38.p7 | 17:78086980 | CTCTGCACCCCTCTG[C/T]AGGCAAATCGGCCAT | 57690 |
rs748178321 | snp | C/T | 7.2869e-05 | 0.00603566 | missense | TNRC6C | GRCh38.p7 | 17:78098367 | CAGACATCAAATCGA[C/T]GTGGTCCTCTGGCCC | 57690 |
rs748202259 | snp | A/G | 1.74439e-05 | 0.00295325 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093154 | CACTTCTGTGCAACA[A/G]CAGCAGGTCAGAATG | 57690 |
rs748222950 | snp | C/G | 1.70974e-05 | 0.00292376 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086493 | TTTTAACTCTTCGTT[C/G]TGTCAACAGGCATAC | 57690 |
rs748226532 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052551 | AAACAGTAAGCCCAG[A/G]AGGTCTGCATGCGGG | 57690 |
rs748277794 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064178 | TCGTAAAACTTAACC[A/G]CTTGGTTCCCGGGTT | 57690 |
rs748296668 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078029 | ACACACACACACACC[A/G]CTTGGAGACATGTCT | 57690 |
rs748305029 | snp | A/G | 1.72725e-05 | 0.0029387 | missense | TNRC6C | GRCh38.p7 | 17:78050084 | CTAACGGTGTGAATG[A/G]GGAATGGGGAAAGCC | 57690 |
rs748309919 | snp | A/C | 3.3525e-05 | 0.00409407 | missense | TNRC6C | GRCh38.p7 | 17:78050011 | GGAAGGGGCAGTGGC[A/C]ACAATGGCGTTGGTA | 57690 |
rs748320141 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088233 | AGACTAGATGATCTC[A/G]TTCCTTAATTATTGT | 57690 |
rs748325073 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105579 | AGAAACAGGCTCTAG[A/G]AAAAATTTCTAAGTT | 57690 |
rs748330531 | snp | A/G | 1.6842e-05 | 0.00290184 | missense | TNRC6C | GRCh38.p7 | 17:78051214 | CCCTCTCCACCGTCC[A/G]TTCGCCGCAAAATGG | 57690 |
rs748359410 | snp | C/G | 0.000160449 | 0.00895538 | missense | TNRC6C | GRCh38.p7 | 17:78104668 | CAGCGACGCTGGCCA[C/G]TGGAACGCCCCGTGC | 57690 |
rs748361447 | snp | G/T | 3.32116e-05 | 0.00407488 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093069 | CCATAGCTGGTCACG[G/T]GCCAAATCTGACAGT | 57690 |
rs748375114 | snp | C/T | 0.000175925 | 0.00937717 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077281 | CTCCCCAGTCAGGCC[C/T]TGGGTGGGATTGCCT | 57690 |
rs748434490 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027353 | GAACATGTTCAAGTG[A/T]TGATGAGAAGGAGCT | 57690 |
rs748447660 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002578 | ATCTTGCTTCCTGCT[A/G]TAATCCCAGAGCACT | 57690 |
rs748449469 | snp | A/G | 0.000207462 | 0.0101827 | missense | TNRC6C | GRCh38.p7 | 17:78104522 | ATCCTGGCCGAGTTC[A/G]CTGGTGAAGAAGAAG | 57690 |
rs748460548 | in-del | -/CCTCAGGTGTCG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094212 | GTCTCGAACTCCTGA[-/CCTCAGGTGTCG]CCCATGCTGCTGGAT | 57690 |
rs748461234 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073179 | TGTAGTCATGGTTTA[A/T]TGGTTAATATGTCCT | 57690 |
rs748475474 | snp | A/C | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011340 | TCCATCTCCTCTGTC[A/C]CCACCCTACCCCCAT | 57690 |
rs748483792 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040637 | GCAGTTTATTCGCCT[A/G]CAGCCAATAGGCAAA | 57690 |
rs748517504 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041447 | CTTTATTTAATAGAC[C/T]CTTAACCTTGAGGAA | 57690 |
rs748554953 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083751 | TCTCTCATGAAACCC[C/T]GGTCAAGAATGGCTG | 57690 |
rs748559233 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095738 | TCTCTTCACGTAGAA[A/G]TTGCTAACCAGAAAG | 57690 |
rs748579812 | snp | A/G | 1.6582e-05 | 0.00287936 | missense | TNRC6C | GRCh38.p7 | 17:78098475 | CTCCAGGGTTAACCA[A/G]TCCCAAGCCCTCCTC | 57690 |
rs748584714 | snp | C/T | 0.000151358 | 0.00869806 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071202 | TGCTACCCACCATGC[C/T]TCCCAAAATGAAATG | 57690 |
rs748600623 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053717 | ATATCAAATTTAATA[C/G]AGTTTAATTAGCATT | 57690 |
rs748609734 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082660 | TCCATATGAACAGGC[A/G]CCCCTCATGCATCCA | 57690 |
rs748612355 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107059 | CATTACATGCGTTCT[A/G]TATATTCGATGGACA | 57690 |
rs748618723 | snp | A/G | 1.7151e-05 | 0.00292835 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086809 | AGACAAGCCATGAGT[A/G]TCCCTTCCCACCTAG | 57690 |
rs748671965 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021932 | ACTTTGGGATATATT[A/G]CCAGGATTTTTCCTC | 57690 |
rs748706744 | snp | C/G/T | 6.64997e-05 | 0.00576594 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087092 | TGCTCCTTACCCTCT[C/G/T]GGTGAGTGTCCCATG | 57690 |
rs748727529 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055491 | TGGGGAATGCATTCC[A/G]CTACATTATGATGGG | 57690 |
rs748733668 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025600 | ACTCATTTGGGTAAA[A/T]ACCTATTAGCTTTTC | 57690 |
rs748745167 | snp | C/T | 1.70504e-05 | 0.00291975 | missense | TNRC6C | GRCh38.p7 | 17:78049691 | TGCCAAACTGGGGCA[C/T]GGCTGTTGGTATGGG | 57690 |
rs748749054 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006021 | ATGTAGACACATGCA[C/G]TCTCACAGCTAATAC | 57690 |
rs748758524 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010081 | ACAGGCAGGGTTTCG[C/T]CCTGTTGCCCAGGTT | 57690 |
rs748789420 | snp | C/T | 1.65784e-05 | 0.00287905 | missense | TNRC6C | GRCh38.p7 | 17:78098447 | AGAAACAGTACTGCA[C/T]CCACGAGGCCACCTC | 57690 |
rs748798503 | snp | A/G | 1.80549e-05 | 0.00300452 | missense | TNRC6C | GRCh38.p7 | 17:78050632 | GCAAACACAGGTTGG[A/G]GAGACAGCAACAACA | 57690 |
rs748871958 | snp | C/T | 1.71787e-05 | 0.00293071 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098380 | GACGTGGTCCTCTGG[C/T]CCTACCTCCCACACG | 57690 |
rs748879697 | snp | C/G | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78048933 | AGCCAACTGCAGCTG[C/G]GATAAAGTGATAATA | 57690 |
rs748890340 | snp | C/T | 3.32817e-05 | 0.00407919 | missense | TNRC6C | GRCh38.p7 | 17:78067880 | AAGAAAGCACCTCCT[C/T]CTGCAGCTCCTGGGG | 57690 |
rs748897968 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073440 | TGCCTTGCCCCAGAA[C/T]GGACTTGCCTAGGGG | 57690 |
rs748915651 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101860 | CGGTACACCCACAAC[C/G]TTCCAGCATGGGCGT | 57690 |
rs748957371 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042127 | TGTAATCCTTTTTAA[-/T]TTTAATCACTTAAGA | 57690 |
rs748967902 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035065 | ACCAACTAGTCCTTC[-/T]CATTTCTCATCTAAA | 57690 |
rs748974112 | snp | C/T | 2.03818e-05 | 0.00319225 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104677 | TGGCCACTGGAACGC[C/T]CCGTGCCTGGGTGGC | 57690 |
rs749000530 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016821 | TAAACCATTCTTTAC[A/G]TAGATTAGCAATCAA | 57690 |
rs749033650 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069477 | CAACCTTGAACTCCT[A/G]GGCTCGAATTGTCCT | 57690 |
rs749044503 | in-del | -/AGA | | | cds-indel | TNRC6C | GRCh38.p7 | 17:78105631 | TGTGCGTGTTGAAAC[-/AGA]AGTGTGTGTGTGTGT | 57690 |
rs749078785 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055300 | GGGCCGGGATCTTCA[C/G]TATCACTGTTGTCCA | 57690 |
rs749085508 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | TNRC6C | GRCh38.p7 | 17:78079418 | TGGCAATCTGGGTAT[A/G]TTTGGCAATAGTGGA | 57690 |
rs749107439 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005984 | TTTTTTCCACTGGAC[C/T]ATCACATGTACACAA | 57690 |
rs749122103 | snp | C/T | 0.000114084 | 0.00755174 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051414 | CCCGCACCAGGCCGG[C/T]ACTCAGCTGAATCGA | 57690 |
rs749127409 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036890 | GATCACACCACTGCA[C/T]TCCAGCCTGGGTGAC | 57690 |
rs749166424 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097161 | TGAGGCTGCTGTGCA[C/T]TGTGATCATGCCTGT | 57690 |
rs749181509 | snp | C/G | 1.65616e-05 | 0.00287759 | missense | TNRC6C | GRCh38.p7 | 17:78049593 | CAGCGCACAACCTCA[C/G]AACCTTAACACTGAT | 57690 |
rs749200979 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079345 | CTACCTCCAAACAAT[C/G]TTACTCTAATGCCTG | 57690 |
rs749212856 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080369 | GAGAATCGCTTGACC[C/T]GGGGAGGTGGAGATT | 57690 |
rs749218258 | snp | C/G/T | 0.00149148 | 0.0272689 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077346 | ACAGGTAAGGCTGTT[C/G/T]GGAGAGAGCAAAACA | 57690 |
rs749255380 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092239 | GGAAGCATTCTAAAA[A/G]GAAAAAGGAAACTAT | 57690 |
rs749258605 | in-del | -/ACC | 0.00653889 | 0.0568039 | cds-indel | TNRC6C | GRCh38.p7 | 17:78051340 | AGTACCACGACCAAT[-/ACC]ACCACCACCACCACC | 57690 |
rs749265019 | snp | A/C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007091 | CAAATGATTCCCCCC[A/C/T]ACCTCGGCCTGCCAA | 57690 |
rs749297392 | snp | C/T | 1.68875e-05 | 0.00290576 | missense | TNRC6C | GRCh38.p7 | 17:78049240 | GCCACAGGCTCCAGC[C/T]CTGGCCTGGCTCACT | 57690 |
rs749305013 | in-del | -/CTT | 1.72493e-05 | 0.00293672 | cds-indel | TNRC6C | GRCh38.p7 | 17:78049154 | CACTCGTCCAAAGCC[-/CTT]CTAATCAGAGTGCCC | 57690 |
rs749320390 | in-del | -/AG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074159 | ACCTCAGCACCACAC[-/AG]GGGGACCATTTTAAA | 57690 |
rs749321347 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002402 | GGACATGTGGCTCCC[A/G]ACTGTAACAGAAAAA | 57690 |
rs749333046 | snp | A/G | 1.66263e-05 | 0.00288321 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086909 | GCACCAGCGCCAGCT[A/G]GCCCAGGCCCTGCTC | 57690 |
rs749353543 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028923 | GACTATTGAGGCGCC[A/G]ACTCTTGCACTTTAC | 57690 |
rs749359028 | snp | A/G | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031651 | AGCCAGCTGCATCCC[A/G]TTACCTGCCTCGTGA | 57690 |
rs749377367 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062973 | TGTAAAGACTGGGTA[C/T]GGTAACTCACATCTG | 57690 |
rs749422983 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087199 | GGAGGACTGGCCAGC[A/G]CTGAAACCATAGCCT | 57690 |
rs749423550 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074662 | TGCAGATACAGGACT[C/T]GGTGAATGGAGAGGC | 57690 |
rs749438467 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024473 | CCAGGTTCACGCCAT[C/T]CTCCTGCCTCAGTCC | 57690 |
rs749446971 | snp | A/G | 5.24985e-05 | 0.00512313 | missense | TNRC6C | GRCh38.p7 | 17:78049144 | ACCAATGGCGCACTC[A/G]TCCAAAGCCCTTCTA | 57690 |
rs749461238 | snp | G/T | 1.82374e-05 | 0.00301966 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050235 | CAAAGCGGCATCTTC[G/T]GGAACTACAGCAAGT | 57690 |
rs749478156 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097994 | TGTGGCGTGATGAAG[A/G]ATGGGTGGGGGCCTT | 57690 |
rs749479403 | in-del | -/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105227 | GGGAGGGAGGGAGAC[-/G]TGAAGCCTATTTAAA | 57690 |
rs749492733 | snp | A/C | 1.71026e-05 | 0.00292421 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086819 | TGAGTGTCCCTTCCC[A/C]CCTAGTTAACGCACC | 57690 |
rs749492805 | snp | A/G | 6.62932e-05 | 0.00575693 | missense | TNRC6C | GRCh38.p7 | 17:78093682 | GAGAATGACCCTGAC[A/G]TCACTCCTGGCAGTG | 57690 |
rs749496691 | snp | A/G | 1.7856e-05 | 0.00298792 | missense | TNRC6C | GRCh38.p7 | 17:78050143 | AATGGGAAAGGATCA[A/G]CAGGGTGGGAGAGTC | 57690 |
rs749536478 | snp | A/G | 1.65913e-05 | 0.00288017 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064751 | GGAGAAATGCCTAAT[A/G]TTCACTCAAAGACTG | 57690 |
rs749580789 | snp | A/T | 1.75576e-05 | 0.00296285 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093159 | CTGTGCAACAGCAGC[A/T]GGTCAGAATGTGCTC | 57690 |
rs749584474 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038767 | TTTTCACTTACCAAA[C/T]TGTCAAAACTTTAAA | 57690 |
rs749610181 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072094 | AAAAGAATGAGTCCA[G/T]AATGGCCTCCATGTA | 57690 |
rs749623562 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020740 | TGAAAGCAACAGAAA[A/C]ATTGTTAATGAGGTA | 57690 |
rs749625453 | snp | A/G | 6.51204e-05 | 0.00570578 | missense | TNRC6C | GRCh38.p7 | 17:78091574 | AACTTGCCCAGTGCC[A/G]CTTCCCCCCTGGAGC | 57690 |
rs749713497 | snp | G/T | 1.85153e-05 | 0.00304258 | missense | TNRC6C | GRCh38.p7 | 17:78051026 | ATCCAGGTACAAACT[G/T]GGGGGAGACTTTAAA | 57690 |
rs749722196 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095039 | GGGGCACCAGGGTTG[C/T]GCCAGACAGGAAAAT | 57690 |
rs749747489 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063968 | TGCAAATGCTGACAA[A/T]TGAATAGGCTTTAAT | 57690 |
rs749752223 | snp | A/G | 1.66081e-05 | 0.00288163 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050901 | CTTGGGGGATGGGAA[A/G]AAAAATGGATCTGGA | 57690 |
rs749763041 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105390 | GTTCCCCTGGATCCG[C/T]CTATGCACATTACCC | 57690 |
rs749772536 | snp | A/G | 3.6507e-05 | 0.00427226 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073031 | AAACTCTGTTTTCCT[A/G]CACAGAGAGAGCCAG | 57690 |
rs749777437 | snp | C/T | 2.92779e-05 | 0.00382597 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78102493 | TGCCTGGAGCACCGA[C/T]ACCTCAGGAAGAACC | 57690 |
rs749817283 | snp | C/G/T | 0.000187988 | 0.00969322 | missense | TNRC6C | GRCh38.p7 | 17:78104565 | TAGCCCAAGGCCAGG[C/G/T]GCTGCCACCCACTTC | 57690 |
rs749868354 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019983 | AATTTATCTGTGTTA[C/T]AAGAATAGATCCAGA | 57690 |
rs749887747 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78031808 | TCCCCTACCTGGAGC[C/T]GGAACACAGCATCAT | 57690 |
rs749902678 | snp | C/T | 3.25209e-05 | 0.00403229 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102464 | ACCAGGTTCTCCCCT[C/T]TTGTTGCAGGTTCTG | 57690 |
rs749929638 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042518 | GTTCATTTCAGAGTT[C/T]TCATTCATTTCAAAA | 57690 |
rs749933058 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041318 | TGCTAAAGATCTGCC[G/T]CACGGAGCAGAGACT | 57690 |
rs749934292 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085964 | GTATTGACTCTGTGA[C/T]TTTTTTTAGTTCTGC | 57690 |
rs749973278 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038825 | ACACAGTACTATGGA[-/T]TGAGTGCTTATCATT | 57690 |
rs749978996 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054948 | TGCGGACTACTGTAC[A/G]CTACCATACACCACT | 57690 |
rs749981420 | snp | C/T | 2.04899e-05 | 0.00320071 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075115 | TTGTTTACAACATTG[C/T]TTCTGTTTGTTGTGC | 57690 |
rs749985983 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054334 | ACCACTGCAGACTAC[C/T]GCACACTACTGCAGA | 57690 |
rs749997078 | snp | C/T | 3.32829e-05 | 0.00407925 | missense | TNRC6C | GRCh38.p7 | 17:78050870 | ATTGGGCAGATTCAT[C/T]GTCTGTCCTTGGACA | 57690 |
rs750040801 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096510 | CTAAAGAGGTCCCTT[G/T]CAGCAGGGCAGCTGC | 57690 |
rs750043672 | snp | G/T | 1.6886e-05 | 0.00290564 | missense | TNRC6C | GRCh38.p7 | 17:78049207 | AGTAATGGAAGTGCG[G/T]CCAGAGTGTGGGGTG | 57690 |
rs750084376 | snp | A/T | 5.00079e-05 | 0.00500015 | missense | TNRC6C | GRCh38.p7 | 17:78086868 | GTTGCGCGCACAATC[A/T]CTAATCTGCAGCAGC | 57690 |
rs750090556 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095655 | TTGCTCCACTCTGGT[A/T]CCTCTCTTGGTTGTG | 57690 |
rs750143798 | snp | A/C | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011237 | GAGAAGAAATAGATA[A/C]GTGTTGGCATATATT | 57690 |
rs750147170 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006964 | ATCACCCCACCCCCA[A/C]CCCATAAGCTGGGGT | 57690 |
rs750221437 | snp | A/G | 5.36217e-05 | 0.00517764 | missense | TNRC6C | GRCh38.p7 | 17:78050608 | AACGCGCCACCTGCC[A/G]CTGTGCCAGCAAACA | 57690 |
rs750226876 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092069 | ACTGGTGTCCCCATC[A/G]GGAACTCTTTACTGA | 57690 |
rs750269752 | snp | A/G | 3.49138e-05 | 0.004178 | missense | TNRC6C | GRCh38.p7 | 17:78049799 | CTGAAGGAATAAGCA[A/G]TTCTGTGTGGGGACT | 57690 |
rs750271914 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074274 | ATATCTGAGGCTCAA[C/G]CTGAACTGGGAACTT | 57690 |
rs750285570 | snp | C/T | 1.65905e-05 | 0.0028801 | missense | TNRC6C | GRCh38.p7 | 17:78083089 | GCAAAAAACATTGGT[C/T]TCAACCCTGCACTAT | 57690 |
rs750289291 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103647 | GTGTCCTGAGCCACC[A/G]TAGCAGAATCCCACA | 57690 |
rs750295669 | snp | A/G | 1.65888e-05 | 0.00287996 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049905 | ATTAAGTGCTAAACA[A/G]AATGGATCCAGCAGT | 57690 |
rs750310637 | snp | A/C | 1.66236e-05 | 0.00288297 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079577 | GGACTGAGCAACAGG[A/C]TATAGATGCCAGTGT | 57690 |
rs750389007 | snp | G/T | 3.96173e-05 | 0.00445051 | missense | TNRC6C | GRCh38.p7 | 17:78091562 | AACTCCATGGATAAC[G/T]TGCCCAGTGCCGCTT | 57690 |
rs750441111 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056302 | AGCTGGGATTACAGG[C/T]GATCACCACCATGCC | 57690 |
rs750445057 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095425 | AAGGAAATGGCATCT[C/T]CAGCCCTGAGCCTAA | 57690 |
rs750447794 | in-del | -/AT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062052 | GGTCTTTAGCAACAC[-/AT]GAGTTATTTTAGCTT | 57690 |
rs750447890 | in-del | -/TGGCACTGA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090087 | AAGTAGGCAGCCCTG[-/TGGCACTGA]TGGGCTTGCAAAGGC | 57690 |
rs750472258 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070046 | GAATGTATTCATGTT[A/C]AAAAAAATATAGTTT | 57690 |
rs750523611 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024333 | TTATTAATAGGCTGT[A/G]TTATTTAGAGCAGTT | 57690 |
rs750525186 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069236 | CAGCCAGAAACCCAG[G/T]AGAAAAAGGAGCACA | 57690 |
rs750529553 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098857 | GCCCCACACTGGGCC[A/G]TCAGAGGCCTGCACA | 57690 |
rs750540866 | snp | A/G | 1.66045e-05 | 0.00288132 | missense | TNRC6C | GRCh38.p7 | 17:78067829 | CCAGCCAGTGGGAGG[A/G]TGAAGAAGGGGACGT | 57690 |
rs750558064 | snp | C/T | 1.66275e-05 | 0.00288331 | missense | TNRC6C | GRCh38.p7 | 17:78049360 | GGCATTAATCTTAAC[C/T]TTAATCCTAATGCCA | 57690 |
rs750574442 | snp | C/T | 1.66529e-05 | 0.00288551 | missense | TNRC6C | GRCh38.p7 | 17:78050519 | GTGCAGCTACTCAGG[C/T]TTCAAACTCAGGGGG | 57690 |
rs750596997 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081153 | GGAAGGGGCAAACAG[A/G]CTTCCTCAGGCCTCT | 57690 |
rs750602378 | snp | A/G | 0.000201755 | 0.0100418 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097868 | GTGTTGCAGGTACGC[A/G]CCTGGCCTCTAGACT | 57690 |
rs750709012 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007974 | TGGATTTGTTTTAAA[C/T]ATTTTCAAGGAACTT | 57690 |
rs750724099 | snp | A/G | 8.56803e-05 | 0.00654468 | missense | TNRC6C | GRCh38.p7 | 17:78050060 | GGGGCCACCCCAGCC[A/G]AAGCACCTCTAACGG | 57690 |
rs750732687 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051820 | AGGATAGACATGGTT[C/T]AGAACTTGGGCAAGT | 57690 |
rs750737262 | snp | C/T | 1.65965e-05 | 0.00288062 | missense | TNRC6C | GRCh38.p7 | 17:78093055 | CCCGTAGCTGTTCCC[C/T]ATAGCTGGTCACGTG | 57690 |
rs750740458 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007382 | AGCATCAAGGTTTAC[A/G]TTTTTCTCAGACTCT | 57690 |
rs750740563 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037229 | AGCAGTGCCACACTC[A/G]GCTTGCACAGCTCTG | 57690 |
rs750743524 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003364 | GGAAAAAAGATATGC[A/G]GAAAACTTAGAAGAT | 57690 |
rs750823410 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78079443 | AGTGGAGCAGCACAA[A/G]CCAGGACCATGCAGC | 57690 |
rs750852215 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075763 | AATGTTTAGCCAGTC[C/T]GGTCACAGCTCAGCC | 57690 |
rs750879544 | snp | A/G | 9.10622e-05 | 0.00674706 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051333 | CCAGAGCAGTACCAC[A/G]ACCAATACCACCACC | 57690 |
rs750904063 | in-del | -/ATA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070338 | TCCATATGCTCCATG[-/ATA]TAGCTGTGGCAGGCT | 57690 |
rs750907442 | snp | A/G | 3.3345e-05 | 0.00408306 | missense | TNRC6C | GRCh38.p7 | 17:78104489 | TGCTGTTGCAGGTGC[A/G]TCCTGGGAAACACTA | 57690 |
rs750937448 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014948 | CTAAGGCAACTTCTC[G/T]CCACAATGTTTGCTG | 57690 |
rs750947406 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044182 | TTTGAGCTATCAGTT[C/T]CTCTTGTACTAACTT | 57690 |
rs750989509 | snp | C/G | 7.78665e-05 | 0.00623916 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104441 | CCACGAACTCAGCAG[C/G]ACTTGGGGTGGCCCT | 57690 |
rs750993133 | snp | G/T | 6.51487e-05 | 0.00570702 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075298 | GAATATAGGTGGTTT[G/T]TTGTTTTTGCTTTTT | 57690 |
rs751018191 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030423 | CCCACCGTGGCCTCC[C/T]TAGACTTTTTATGTG | 57690 |
rs751034747 | snp | A/G | 1.9557e-05 | 0.003127 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092887 | TTCTGGTGTCTCTCA[A/G]CTGGAGAGTATTCAC | 57690 |
rs751036113 | snp | A/G | 1.65938e-05 | 0.00288039 | missense | TNRC6C | GRCh38.p7 | 17:78049919 | AAAATGGATCCAGCA[A/G]TGCTGTGCAAAAGGA | 57690 |
rs751046347 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040049 | CTCCCAGCCCTGGTT[C/T]CAGGTTCTCTTTAGG | 57690 |
rs751069436 | snp | C/T | 3.34191e-05 | 0.0040876 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083205 | TTAGAGCACGCAGGC[C/T]GAGTGCAGATGCACG | 57690 |
rs751078502 | snp | A/C | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010933 | TTGTGAAACAAAGGA[A/C]GTGAGCCTAGCGGCA | 57690 |
rs751126281 | snp | A/G | 3.91903e-05 | 0.00442647 | missense | TNRC6C | GRCh38.p7 | 17:78051146 | CAGGGTGGATCGGGG[A/G]GCCGGTACCGGTCAA | 57690 |
rs751172874 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106402 | CGTCAAGGTGACAGG[C/T]GTTGTGGCCACTGTC | 57690 |
rs751192453 | snp | C/T | 1.95166e-05 | 0.00312376 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075132 | TCTGTTTGTTGTGCT[C/T]CAGGCGCTCTGCTGG | 57690 |
rs751194050 | snp | C/T | 1.66261e-05 | 0.00288319 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78103438 | TCTACACTGCGGACA[C/T]TGTGTTTGCAACATG | 57690 |
rs751229395 | snp | A/G | 2.94573e-05 | 0.00383768 | missense | TNRC6C | GRCh38.p7 | 17:78102488 | GGTTCTGCCTGGAGC[A/G]CCGACACCTCAGGAA | 57690 |
rs751239527 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034043 | TTTCCCCGCCTACTC[A/T]CCATGGCCTACTTTT | 57690 |
rs751268134 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017400 | CATGTTGCATTCCTG[C/T]TCAGGTGGCGGAGCT | 57690 |
rs751295015 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020669 | TAAAAAGTAACAGGC[A/G]GAATTACTTTTAATA | 57690 |
rs751297074 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058266 | GGAGAAAGTGCAAAC[A/T]TAGCATTTATGTGTG | 57690 |
rs751318166 | snp | C/T | 4.4339e-05 | 0.00470824 | missense | TNRC6C | GRCh38.p7 | 17:78098349 | CCTTTCTAGGTAAAC[C/T]GTCAGACATCAAATC | 57690 |
rs751323522 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028185 | CAGGCGTGAGCCATC[A/G]CCCCCCGCTGAAACT | 57690 |
rs751339936 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048308 | TCTTTTCTCTCTTTC[C/T]TTCCGTCACCACTTC | 57690 |
rs751370216 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101593 | GGGTCTCACAGCCTT[C/T]AGAGCTGAGAGCCCT | 57690 |
rs751370894 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061029 | CCATTCTGAAGGAAA[A/G]ATGAAGAATGTATAT | 57690 |
rs751426073 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072998 | CCTTTCCTTTTGTTA[A/G]TTAATGTGCACTAAT | 57690 |
rs751458026 | snp | G/T | 1.66048e-05 | 0.00288134 | missense | TNRC6C | GRCh38.p7 | 17:78093024 | AATCCAGAACAGTGA[G/T]TCACCAGCCAGTCCT | 57690 |
rs751473523 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097317 | TTTATGGCAAATTTT[A/G]TAATAAAAGGCTTGG | 57690 |
rs751479117 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071530 | AGAGCTGGGACTACA[A/G]GCGTGAGCCACCATG | 57690 |
rs751534602 | snp | A/G | 6.99215e-05 | 0.00591235 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067730 | AGGGACATGAATTTG[A/G]TAAGTTCATGTTTGC | 57690 |
rs751544014 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037070 | CATTTTGTCATAATT[C/G]ACCTTTTGATTTACA | 57690 |
rs751550547 | snp | A/G | 1.6591e-05 | 0.00288015 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083103 | TCTCAACCCTGCACT[A/G]TTAACCTCGCCAATT | 57690 |
rs751578514 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036649 | CTTACATAGGCCGGG[C/T]GCGTTGGCTCACACC | 57690 |
rs751578995 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073762 | TATGTTTTTCTGTTT[C/T]AAGACACCTTATTTA | 57690 |
rs751589703 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067108 | AACACTTTGGGATGC[C/T]GAGGCAGGAGGACTA | 57690 |
rs751597009 | in-del | -/AGACAG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066939 | CAGTGATTAAGAATC[-/AGACAG]AGATGCTCATTTCAG | 57690 |
rs751628214 | snp | C/T | 3.565e-05 | 0.00422182 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077247 | CCCAAGCCTGAAGCT[C/T]CCCCTTTCACACAGT | 57690 |
rs751635718 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081088 | AAGATTCAGTGTCTG[C/G]TGAGGGCCCGTTTCT | 57690 |
rs751654983 | snp | A/T | 4.96874e-05 | 0.0049841 | missense | TNRC6C | GRCh38.p7 | 17:78049573 | ACTTCTCAGAATGTG[A/T]CTTTCAGCGCACAAC | 57690 |
rs751673356 | snp | A/G | 3.64644e-05 | 0.00426976 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050664 | AGCGCCAAGTGGCCC[A/G]GGGGTTTGGGGGGAC | 57690 |
rs751688880 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079994 | GCCAAGGACTGAATC[A/G]TGCTTTAATGAGAAA | 57690 |
rs751690806 | snp | A/G | 7.12784e-05 | 0.00596943 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091413 | TTTAGAGGAGCAGGC[A/G]AATCCTAACCGCATC | 57690 |
rs751739837 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091721 | GAGCACTGAAAGTTG[A/G]ATTTAAAATAACCCA | 57690 |
rs751742398 | snp | A/C | 1.65943e-05 | 0.00288043 | missense | TNRC6C | GRCh38.p7 | 17:78049480 | CAAAATATGGGCAAC[A/C]AGAACGGGAACCCAA | 57690 |
rs751759645 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108692 | CCACGCAAAGACCTC[A/G]TGGGCCTGGGTGTCC | 57690 |
rs751760738 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038678 | GCGAGACTCCGTGTC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs751780639 | snp | C/T | 1.67089e-05 | 0.00289035 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087111 | GAGTGTCCCATGGTC[C/T]TCAACAGCCACATCA | 57690 |
rs751787655 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069833 | GGAGGAAGAAAACGT[-/GT]GTGTGTGTGTATGTG | 57690 |
rs751811781 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102372 | TAAAGCACGCAGTGA[C/T]GGCCTGTGCTGTCCC | 57690 |
rs751816139 | in-del | -/TT | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105130 | TTTTTTTTTTTTTTA[-/TT]AGTATAAAAGCTGCT | 57690 |
rs751824517 | snp | A/C | 1.7056e-05 | 0.00292022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093611 | TTCTCATTTTGGTTT[A/C]TTAAACAGAATTCCA | 57690 |
rs751838248 | snp | C/G | 3.54465e-05 | 0.00420975 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050598 | TGGGTGGGTCAACGC[C/G]CCACCTGCCGCTGTG | 57690 |
rs751854569 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018370 | CCTGACCTCGTGATC[A/C]GCCCCGCCTCGGCCT | 57690 |
rs751855701 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087813 | CAGCACTTGAAACCC[A/G]CAGGTCAGTAGAAGA | 57690 |
rs751902437 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082355 | CTTTAACATAACATC[A/G]GTATGCAGAAGTACA | 57690 |
rs751921499 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013066 | AGTCATCTTAAACCC[A/G]TCCATCAGGTCATTA | 57690 |
rs751925601 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005043 | CTTTCTTTCTCTCTC[-/T]TTTTTTTTTTTCAGG | 57690 |
rs751936507 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074449 | AGACTGTCTAATCGT[C/G]CACGTGCGACAACGT | 57690 |
rs751980506 | snp | A/G | 1.89892e-05 | 0.00308127 | missense | TNRC6C | GRCh38.p7 | 17:78104787 | GCAGGGTGATAGGCA[A/G]CCCCACGCCGCTAAC | 57690 |
rs752028839 | snp | C/G | 1.8251e-05 | 0.00302079 | missense | TNRC6C | GRCh38.p7 | 17:78050195 | CTACCGTACAGCCTG[C/G]TGGTGAACACATGAA | 57690 |
rs752034180 | snp | C/T | 1.67728e-05 | 0.00289588 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064702 | TCATTATTTTCTCTA[C/T]CCCTTGGAACCTTTT | 57690 |
rs752045124 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013677 | ACAGCATCAACAAAG[A/G]AGCCCAAACTTGGCA | 57690 |
rs752099640 | snp | C/G | 3.42683e-05 | 0.0041392 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093136 | CCAGGTAAGACCATG[C/G]AACACTTCTGTGCAA | 57690 |
rs752110503 | in-del | -/CT | 1.73249e-05 | 0.00294315 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067745 | ATAAGTTCATGTTTG[-/CT]CTGTTTCTAGCTTCA | 57690 |
rs752119878 | snp | A/G | 0.000152219 | 0.00872274 | missense | TNRC6C | GRCh38.p7 | 17:78104652 | CCCATGGCCTGGTAC[A/G]CAGCGACGCTGGCCA | 57690 |
rs752140669 | snp | C/T | 1.65699e-05 | 0.00287831 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079390 | TTAATTCTGTCCCTG[C/T]GCAGATACCGAGTGG | 57690 |
rs752207850 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020513 | AACAGGTAATTATTT[A/C]GCGGTTTCTGAGAAA | 57690 |
rs752209859 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068168 | AGGTGTCCAGAGAAC[-/T]TTATTGTAGCAGAGA | 57690 |
rs752221819 | snp | A/G | 0.000181736 | 0.00953073 | missense | TNRC6C | GRCh38.p7 | 17:78075252 | TCCAAAGAGTCTTCC[A/G]TGGACCGCCCCACCT | 57690 |
rs752222598 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063795 | AGGTGATCTGTGTCT[A/G]TGATGGTCAAAAGAT | 57690 |
rs752222739 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076188 | GCCATTGCACTCCAG[C/T]CTGGACGAGAGAGCG | 57690 |
rs752264229 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032976 | ACTGACCAAGAATAT[A/G]GTCTCATCTATTTAG | 57690 |
rs752292297 | snp | G/T | 6.63867e-05 | 0.00576099 | missense | TNRC6C | GRCh38.p7 | 17:78049924 | GGATCCAGCAGTGCT[G/T]TGCAAAAGGAAGGAA | 57690 |
rs752311987 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105020 | CAAAACAGTGCGGGC[C/T]GCGGTGGGTCAGCGT | 57690 |
rs752323954 | snp | A/C | 4.15274e-05 | 0.00455653 | missense | TNRC6C | GRCh38.p7 | 17:78051154 | ATCGGGGGGCCGGTA[A/C]CGGTCAAACAGAAGG | 57690 |
rs752340608 | snp | A/G | 8.88849e-05 | 0.00666593 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051312 | GGATAGAAACAACCC[A/G]GTCATCCAGAGCAGT | 57690 |
rs752361916 | snp | C/T | 7.22726e-05 | 0.00601091 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104464 | GTGGCCCTGTTCACG[C/T]GCCCCATCTTGCTGT | 57690 |
rs752384970 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026844 | TTCCAATGGTGACCG[C/T]TGGAATGAAAATAGA | 57690 |
rs752436420 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039892 | TGGAACAAGAGTGGC[A/G]GAAATGTAGGGTGGT | 57690 |
rs752441297 | snp | A/C | 3.34359e-05 | 0.00408862 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087113 | GTGTCCCATGGTCTT[A/C]AACAGCCACATCAGG | 57690 |
rs752451905 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033610 | GGACGTGGAGGTTGC[A/G]GCGAGCCGAGATCAC | 57690 |
rs752462216 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045307 | TATGTAAACTCAACA[C/G]GCATGACTTCATCCT | 57690 |
rs752481048 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070325 | CTGTTTATAGAGCTC[C/T]ATATGCTCCATGATA | 57690 |
rs752485786 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78041008 | GCGGCTCTCGCTGTA[C/T]CCAGCCGACATGTTG | 57690 |
rs752491758 | snp | A/G | 1.66969e-05 | 0.00288932 | missense | TNRC6C | GRCh38.p7 | 17:78098513 | GGTGCCAGCCCCCTC[A/G]GCTGGACCAGCTCCT | 57690 |
rs752508426 | snp | A/C | 1.65622e-05 | 0.00287764 | missense | TNRC6C | GRCh38.p7 | 17:78049585 | GTGTCTTTCAGCGCA[A/C]AACCTCAGAACCTTA | 57690 |
rs752536213 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095353 | AAGGAGATCAACTTG[C/T]GGGGAGGGCAGAAGA | 57690 |
rs752684849 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053096 | CATGTCACGTTGCCC[C/T]CCGACCCCTGACGGT | 57690 |
rs752705366 | snp | A/G | 1.66007e-05 | 0.00288098 | missense | TNRC6C | GRCh38.p7 | 17:78067865 | ATAATGCTGCTTCCC[A/G]AGAAAGCACCTCCTC | 57690 |
rs752747085 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060806 | AAAGCTATGTAAGTG[A/G]CATCTGTGGAACAAG | 57690 |
rs752754338 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034351 | CGTGAGCCACCACCC[A/C]CCAGCCTCCATGGCC | 57690 |
rs752757076 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090456 | TACGTACCGTGTGGC[A/G]TAGTACTTACGGTAA | 57690 |
rs752758448 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091663 | GCTTATTAATCGATC[A/G]TCCTGTTGTATAGCA | 57690 |
rs752767615 | snp | G/T | 1.66261e-05 | 0.00288319 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064727 | CCTTTTTCAGTTTCA[G/T]CAGGCTGGGGAGAAA | 57690 |
rs752774728 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013798 | TAAAGAGCCTGTGGC[C/T]GTATGGAGTATGACA | 57690 |
rs752785281 | snp | C/T | 0.000938526 | 0.0216421 | missense | TNRC6C | GRCh38.p7 | 17:78104796 | TAGGCAGCCCCACGC[C/T]GCTAACCACCCTGCT | 57690 |
rs752813411 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101243 | GGCAGGGGCAAAATG[-/C]CCGCCAGTCTCTTTG | 57690 |
rs752813648 | snp | A/C | 1.65726e-05 | 0.00287855 | missense | TNRC6C | GRCh38.p7 | 17:78079534 | TGCCTCAGTTTCTAT[A/C]CCCTCAGGTCAGACC | 57690 |
rs752818377 | snp | C/T | 1.68701e-05 | 0.00290427 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049675 | ATGCAGACAAATGGA[C/T]TGCCAAACTGGGGCA | 57690 |
rs752857753 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047016 | TATGGAAAAGAATGC[A/G]TTGGTCAGCCAGGTT | 57690 |
rs752933891 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100377 | TATATCCTCTGAAAT[C/G]TAGGTGGAGGTTCCC | 57690 |
rs752956111 | in-del | -/A | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012016 | AGATTGGTTTCTGAT[-/A]CTAAATTGGCCTCTA | 57690 |
rs752958330 | in-del | -/GTGA | 2.70867e-05 | 0.00368003 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78051088 | CCCCAAGACAACAAT[-/GTGA]GTAACTGGGGAGGAG | 57690 |
rs753001465 | in-del | -/TTTTTT | 3.13681e-05 | 0.00396019 | cds-indel | TNRC6C | GRCh38.p7 | 17:78071141 | AGCCGGCTGATCAAA[-/TTTTTT]CAACTCACAGACATG | 57690 |
rs753008082 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016328 | CACAGCCAGTACCTG[C/T]CAGGTCACATGCACT | 57690 |
rs753056178 | in-del | -/TT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015417 | TCCCAGTTAGCATTT[-/TT]ACCTATAAAAAGTTA | 57690 |
rs753070185 | snp | A/C | 1.65957e-05 | 0.00288055 | missense | TNRC6C | GRCh38.p7 | 17:78050480 | CTGAAAGGAAAAATG[A/C]CAATGGGACAGAGGC | 57690 |
rs753077050 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108510 | TACCCGTGCCTGTGC[A/G]CTGGGAGAACAAGGT | 57690 |
rs753077618 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055004 | CCACTGCGGACTACT[A/G]TACACCACTGCAAAG | 57690 |
rs753093808 | snp | G/T | 6.65591e-05 | 0.00576846 | missense | TNRC6C | GRCh38.p7 | 17:78049323 | AAGTCAGAATTGCTG[G/T]GGTGCTTCCAACTCC | 57690 |
rs753130697 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067012 | TTCGCGTGGTTCCTA[A/T]GCAAGGATGAGATAC | 57690 |
rs753174079 | snp | C/T | 1.82517e-05 | 0.00302084 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050211 | TGGTGAACACATGAA[C/T]TCCTGGGCCAAAGCG | 57690 |
rs753187902 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066288 | ATCTTTTCTTTGGAC[A/G]TTATTAGATGTCCTA | 57690 |
rs753191295 | snp | C/T | 1.78733e-05 | 0.00298937 | stop-gained | TNRC6C | GRCh38.p7 | 17:78050326 | GGAGAAGGCCGAAGG[C/T]GAGATAAAGGGATTA | 57690 |
rs753225649 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082657 | TTATCCATATGAACA[A/G]GCGCCCCTCATGCAT | 57690 |
rs753233304 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079042 | GTTGCAGTGAGCTGA[A/G]ATCGCACTACTGCAT | 57690 |
rs753251635 | in-del | -/TGGGC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043215 | AGCCTGAAACTTCAG[-/TGGGC]TGGGCTGGGCTGGGC | 57690 |
rs753269916 | snp | A/G | 0.00015097 | 0.0086869 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093630 | AACAGAATTCCATCC[A/G]GGAGTTCCATGGAAA | 57690 |
rs753275966 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006665 | CTGTCTGGTTTAGTA[C/T]CAGCTATATTCTTCA | 57690 |
rs753278448 | in-del | -/GAGTGCCCAGGGC | 1.80869e-05 | 0.00300718 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78050306 | CACTGGGAGGGAAGG[-/GAGTGCCCAGGGC]AACGGGAGAAGGCCG | 57690 |
rs753279035 | snp | A/C | 3.44851e-05 | 0.00415227 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064868 | GGGTGGGGAGATCAC[A/C]CTGCAGAGCCGCCGG | 57690 |
rs753296634 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029855 | AGCCAAGGCCTACAC[A/G]AGGTCAGGATCATCA | 57690 |
rs753297587 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037584 | GCGTCGCAGATGGAG[-/T]GACCTGCATGCATGA | 57690 |
rs753342383 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030867 | ACTTTAGGAGGCTGA[A/G]GCGAGCGGATCACTT | 57690 |
rs753445282 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086219 | ACTGCAATCCCAGCT[A/G]CTCGGGAGGCTGAGG | 57690 |
rs753452794 | snp | A/G | 2.15841e-05 | 0.00328505 | missense | TNRC6C | GRCh38.p7 | 17:78049087 | GGGAGTGCCCAGGGC[A/G]ACTTCACTGGACATA | 57690 |
rs753453332 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102588 | GCATGATCCAGGGAG[A/G]GTTCCCGCTTGGCCC | 57690 |
rs753480805 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013287 | TTGTGCTTTAGAAAG[A/G]TCACTGAACCTGCAG | 57690 |
rs753490243 | snp | A/G | 1.69306e-05 | 0.00290947 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093123 | CATCAACTGGCCCCC[A/G]GGTAAGACCATGCAA | 57690 |
rs753498821 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084937 | GCGCCTGGCCAGAGA[C/T]TGTTTTTCCATCTGT | 57690 |
rs753503272 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101685 | ATACTAGATTAACTA[C/T]AAGTATCCCTTATGG | 57690 |
rs753571939 | snp | C/T | 6.83177e-05 | 0.00584416 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064674 | TATATTTTTGCTTTT[C/T]TCTGATGCACTTTCA | 57690 |
rs753600112 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055974 | GAGGTTAGAACCACA[G/T]TGCATTTGTTGGGGG | 57690 |
rs753609844 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051934 | AAAGGTCCCAGATAC[A/G]GAAGACCAGTTCTCA | 57690 |
rs753623875 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027515 | AAAAACAGAGAAATA[-/C]TTGTAAAGCAAGGAA | 57690 |
rs753628328 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081358 | GCACTGGGCACTGCA[C/T]TGAGGGTAATTCTCG | 57690 |
rs753651012 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081957 | AGACTTTCCTTCTTC[C/T]TTCCCTCCTTTCTTT | 57690 |
rs753657927 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063535 | TGTTTCCACAAGGGA[C/T]CAATCCCTGAGGATG | 57690 |
rs753663998 | snp | C/T | 1.67458e-05 | 0.00289355 | missense | TNRC6C | GRCh38.p7 | 17:78050836 | AGATCAAATCCAGCC[C/T]GGAGTGCAGGAGGGG | 57690 |
rs753667005 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038219 | AATATGAATAAAATC[A/T]GAGAGGACATGTTTA | 57690 |
rs753704938 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020471 | TTGTAGTTTCTCAAT[C/G]TCTGTTTCACTTTCA | 57690 |
rs753713215 | snp | C/G | 6.99974e-05 | 0.00591555 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091428 | GAATCCTAACCGCAT[C/G]TCTCTCTTTAGCTGG | 57690 |
rs753714550 | snp | A/G | 1.82677e-05 | 0.00302217 | missense | TNRC6C | GRCh38.p7 | 17:78091548 | AGTGGACGCACCCCA[A/G]CTCCATGGATAACTT | 57690 |
rs753753021 | snp | A/G | 3.3274e-05 | 0.00407871 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050871 | TTGGGCAGATTCATC[A/G]TCTGTCCTTGGACAC | 57690 |
rs753791864 | snp | A/C | 0.000795229 | 0.0199244 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104889 | CGACCCCTCCCGGGA[A/C]CCCTCCCGGCTGGGC | 57690 |
rs753818548 | snp | C/T | 6.77025e-05 | 0.00581779 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102457 | CTTGTCAACCAGGTT[C/T]TCCCCTCTTGTTGCA | 57690 |
rs753822019 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016188 | TAGAGCACAGTGCCA[C/T]TGCCGCAGACCAGGG | 57690 |
rs753836955 | snp | C/T | 1.68803e-05 | 0.00290515 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098533 | GACCAGCTCCTACTC[C/T]TCGGGTAAGCTCCAT | 57690 |
rs753852973 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089326 | AAGAATTCATGCAGT[A/G]AATCTTTGAAATTAG | 57690 |
rs753882334 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059010 | AGATTTAGGAAGCTT[C/G]TACCTAAAAAGATGA | 57690 |
rs753884472 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045767 | TTTTTAATCAGACTG[C/T]TCTGCCGCCTGATTT | 57690 |
rs753885680 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78071101 | GCATGAAGACGTCTG[A/G]CAAGCAGGATGAGGC | 57690 |
rs753886770 | snp | C/T | 1.6601e-05 | 0.00288101 | missense | TNRC6C | GRCh38.p7 | 17:78050489 | AAAATGACAATGGGA[C/T]AGAGGCCTGGGGTTG | 57690 |
rs753910149 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100130 | GCTGTCTTCACGGGC[G/T]GGTATTGTCTGCAGC | 57690 |
rs753935701 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057961 | AATGCAGTATAGCTT[C/G]CTAAACTGGATTGTC | 57690 |
rs753945386 | snp | C/T | 1.65949e-05 | 0.00288048 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083070 | ACAGCTTTTGCAGTT[C/T]GCAGCAAAAAACATT | 57690 |
rs753971481 | in-del | -/GCAGGGCCAGATCACAGACTGCAGGAGCCACGGAAGGGTGCCTGGGG | 3.7342e-05 | 0.00432083 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78075257 | GAGTCTTCCGTGGAC[lengthTooLong]CGCCCCACCTTTCTT | 57690 |
rs753976934 | snp | A/G | 7.01262e-05 | 0.005921 | missense | TNRC6C | GRCh38.p7 | 17:78050341 | CGAGATAAAGGGATT[A/G]TAGACCAAGGGCACA | 57690 |
rs753982351 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026650 | TGGGAGTCTTACTGC[C/T]CAGGACCACGTGGAC | 57690 |
rs754045452 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098850 | TGTGGCTGCCCCACA[C/T]TGGGCCATCAGAGGC | 57690 |
rs754045747 | in-del | -/GACCCCTCCCGG | 0.000616523 | 0.0175465 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104874 | AGCACCAGGAGAGCC[-/GACCCCTCCCGG]GACCCCTCCCGGGAC | 57690 |
rs754054201 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014390 | GCCAGTAGGCATTAA[C/T]GCTGTCTTGATTACT | 57690 |
rs754097699 | in-del | -/TTTG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035156 | CACCATTCCAATGAC[-/TTTG]TTTGATTTTGTCAGT | 57690 |
rs754107231 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035301 | CAATCCACTTTCCAG[A/C]CCCACCACCTCCTGT | 57690 |
rs754119082 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079555 | AGGTCAGACCCACAT[C/T]CAAGCAGGACTGAGC | 57690 |
rs754149771 | snp | C/T | 0.000812678 | 0.0201415 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104806 | CACGCCGCTAACCAC[C/T]CTGCTGCCTGGGGAC | 57690 |
rs754162902 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045217 | CCAGTCAAGACATGA[A/G]GGTGCTTGGAACAGG | 57690 |
rs754165566 | snp | A/G | 1.65894e-05 | 0.00288 | missense | TNRC6C | GRCh38.p7 | 17:78103472 | CTCTTATCACATTCC[A/G]CCTGAATCTGACTCA | 57690 |
rs754181128 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025296 | GTTTTGCCTTCTCCA[A/G]AATGTCACGTAGTTG | 57690 |
rs754181598 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039415 | CATTGGGCAGAAGCT[C/T]CATTGGTTTTGTAGC | 57690 |
rs754235349 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034117 | GAAATGCGATGGCAC[A/C]GTTTTGGCTCACCAC | 57690 |
rs754248922 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066028 | CTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGGCC | 57690 |
rs754256812 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003796 | TGGCCAGGCTTGGTG[C/T]GTCACACTGGTAATC | 57690 |
rs754301770 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078861 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACAA | 57690 |
rs754305823 | snp | C/T | 7.54006e-05 | 0.00613959 | missense | TNRC6C | GRCh38.p7 | 17:78075258 | GAGTCTTCCGTGGAC[C/T]GCCCCACCTTTCTTG | 57690 |
rs754323175 | snp | A/G/T | 6.6492e-05 | 0.0057656 | missense | TNRC6C | GRCh38.p7 | 17:78049340 | GTGCTTCCAACTCCA[A/G/T]TGCTGGCATTAATCT | 57690 |
rs754327462 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090292 | AGACAGGACAGACAC[A/T]CTCTGGTTTGCCACA | 57690 |
rs754332371 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077780 | ATCTCTTGCAAGGTG[A/G]TTCTCAGGAGTCACA | 57690 |
rs754337933 | in-del | -/TG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030316 | ACCACACCTGGCTTG[-/TG]TGTGTGTGCGTGTGT | 57690 |
rs754339705 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005174 | TTGATGGTTAAAAAA[C/T]GAGAATCTAAGCCTG | 57690 |
rs754353969 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107053 | CATTGCCATTACATG[C/T]GTTCTATATATTCGA | 57690 |
rs754372690 | snp | C/T | 0.000100185 | 0.00707691 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097865 | CTAGTGTTGCAGGTA[C/T]GCGCCTGGCCTCTAG | 57690 |
rs754381689 | snp | C/T | 4.96866e-05 | 0.00498406 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087014 | CAGCTTCCCCTCGCA[C/T]CCACAGACTCCCGGC | 57690 |
rs754417727 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057144 | TGCTGAAAGTATGTT[-/A]AGTTTAGTATATTGT | 57690 |
rs754440566 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019509 | TTGGAAAGAAAATTG[C/T]TTTAAAAGACTGTTG | 57690 |
rs754475470 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092354 | TTTGGTTCTGTATGA[A/C]TTTTTAACATCCACT | 57690 |
rs754481810 | snp | G/T | 1.6591e-05 | 0.00288015 | missense | TNRC6C | GRCh38.p7 | 17:78083110 | CCTGCACTATTAACC[G/T]CGCCAATTAATCCTC | 57690 |
rs754493499 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030874 | GAGGCTGAGGCGAGC[A/G]GATCACTTGAGGTCA | 57690 |
rs754593435 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074383 | TTACAAATTTTAGCA[A/G]GTAGGCCAGCTTTAC | 57690 |
rs754601203 | snp | C/T | 0.000137826 | 0.00830026 | missense | TNRC6C | GRCh38.p7 | 17:78049816 | TCTGTGTGGGGACTG[C/T]CCCCAGGTAACCCTG | 57690 |
rs754621586 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030089 | AACCAGTAATATAGT[C/T]ATTATGAACCATTAT | 57690 |
rs754636551 | snp | C/T | 1.65982e-05 | 0.00288077 | missense | TNRC6C | GRCh38.p7 | 17:78103463 | AACATGGGCCTCTTA[C/T]CACATTCCACCTGAA | 57690 |
rs754644508 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095776 | AGGCCGAGCACAGTG[A/G]CTTACACCTGTAATC | 57690 |
rs754652867 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057886 | AATCATTTTTGTCCT[A/G]TGCTTGTTGATATTA | 57690 |
rs754678385 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086223 | CAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57690 |
rs754679440 | snp | A/C | 0.00467936 | 0.0481434 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050601 | GTGGGTCAACGCGCC[A/C]CCTGCCGCTGTGCCA | 57690 |
rs754691309 | snp | A/G | 1.67711e-05 | 0.00289573 | missense | TNRC6C | GRCh38.p7 | 17:78050993 | GTGGCTGGGGCAACA[A/G]CACAAATACAAAGGC | 57690 |
rs754694612 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042914 | ATTTTAATTAGCTCA[A/G]TATGCAATACAGTCC | 57690 |
rs754695843 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084773 | AGCTGGGATTACAGG[C/T]GCCCGCCACCACGCC | 57690 |
rs754713320 | snp | C/T | 0.000543979 | 0.0164831 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091570 | GGATAACTTGCCCAG[C/T]GCCGCTTCCCCCCTG | 57690 |
rs754742067 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069483 | TGAACTCCTGGGCTC[A/G]AATTGTCCTCCTGCC | 57690 |
rs754754821 | snp | G/T | 1.66308e-05 | 0.00288359 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098410 | GCAAGCCTCTCTGTC[G/T]CATGAACTATGGAAG | 57690 |
rs754758004 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082129 | CTCTTTCTTTGTTCC[C/T]AGGCAGATTGGCAGG | 57690 |
rs754758856 | snp | C/G | 1.6563e-05 | 0.00287771 | missense | TNRC6C | GRCh38.p7 | 17:78087038 | TCCCGGCCTACCTGA[C/G]CTGCAGACCAAAGAG | 57690 |
rs754773527 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085227 | ATCTTTTAGTTATAC[A/G]GTAAGTTTTTATTGA | 57690 |
rs754775207 | snp | A/G | 2.06605e-05 | 0.00321401 | missense | TNRC6C | GRCh38.p7 | 17:78098355 | TAGGTAAACTGTCAG[A/G]CATCAAATCGACGTG | 57690 |
rs754826673 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037432 | TTCAAGGTATTGTAA[C/G]AGAGATAAGCATAGA | 57690 |
rs754846324 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038235 | GAGAGGACATGTTTA[C/T]AGTGTAAATAGCAAA | 57690 |
rs754850980 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008176 | AAAGACTAATGCCGA[A/G]CTGAAGCTAACTGGA | 57690 |
rs754877910 | snp | C/T | 8.08244e-05 | 0.00635655 | missense | TNRC6C | GRCh38.p7 | 17:78051149 | GGTGGATCGGGGGGC[C/T]GGTACCGGTCAAACA | 57690 |
rs754913507 | snp | G/T | 1.67167e-05 | 0.00289103 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050532 | GGCTTCAAACTCAGG[G/T]GGGAAGAACGATGGG | 57690 |
rs754932733 | snp | C/T | 3.31901e-05 | 0.00407356 | missense | TNRC6C | GRCh38.p7 | 17:78067856 | ACGTGTGGAATAATG[C/T]TGCTTCCCAAGAAAG | 57690 |
rs754936950 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081367 | ACTGCATTGAGGGTA[A/G]TTCTCGCTCTGTAAT | 57690 |
rs754948311 | snp | C/T | 1.65674e-05 | 0.00287809 | missense | TNRC6C | GRCh38.p7 | 17:78079398 | GTCCCTGTGCAGATA[C/T]CGAGTGGCAATCTGG | 57690 |
rs755012028 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093378 | GGAAGCACACTGCAC[A/G]CTATCCGGTAAAACT | 57690 |
rs755025976 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002410 | GGCTCCCGACTGTAA[C/T]AGAAAAATAGCCTTT | 57690 |
rs755034691 | snp | A/C | 1.66896e-05 | 0.00288869 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083201 | CAAGTTAGAGCACGC[A/C]GGCCGAGTGCAGATG | 57690 |
rs755106217 | snp | C/T | 0.000312207 | 0.0124902 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104656 | TGGCCTGGTACGCAG[C/T]GACGCTGGCCACTGG | 57690 |
rs755110597 | snp | C/T | 3.3232e-05 | 0.00407614 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104515 | CACTACCATCCTGGC[C/T]GAGTTCGCTGGTGAA | 57690 |
rs755113154 | snp | A/G | 8.36995e-05 | 0.0064686 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077273 | ACAGTGCACTCCCCA[A/G]TCAGGCCCTGGGTGG | 57690 |
rs755119593 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045774 | TCAGACTGCTCTGCC[A/G]CCTGATTTGTATCAC | 57690 |
rs755132250 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058010 | ATTCTGGAGATAAAA[C/T]AACAGTATTAGTCCA | 57690 |
rs755140185 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077730 | CTGCGAGAAAGCACC[A/T]CATTCTCCCCCTTTT | 57690 |
rs755152909 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088140 | TCTGAAAAGAGCGGT[A/G]TATTGTAATCATATG | 57690 |
rs755156990 | snp | C/T | 8.29566e-05 | 0.00643983 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049485 | TATGGGCAACCAGAA[C/T]GGGAACCCAACAGGC | 57690 |
rs755185713 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070130 | TCCGCTCATGAGGAG[C/T]AGAAGTGATTACAGA | 57690 |
rs755210986 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065151 | CGCAGGAGTTTGAGA[C/T]CAGCCTAGGCAGCAT | 57690 |
rs755237901 | snp | A/C/T | 5.01704e-05 | 0.00500831 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087112 | AGTGTCCCATGGTCT[A/C/T]CAACAGCCACATCAG | 57690 |
rs755264683 | snp | A/G | 3.55492e-05 | 0.00421585 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067965 | ACACCCTGAAAACCA[A/G]AGGTACTTCAGACAC | 57690 |
rs755281883 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006492 | TTCTTCTTCTTCTTC[-/T]TTCTTCTTCTTCTTC | 57690 |
rs755315134 | snp | A/C | 1.6641e-05 | 0.00288448 | missense | TNRC6C | GRCh38.p7 | 17:78086889 | CTGCAGCAGCAGATC[A/C]AGCAGCACCAGCGCC | 57690 |
rs755332722 | snp | C/T | 3.46675e-05 | 0.00416323 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086630 | ATGAGCTATAATTTT[C/T]CCTGATAGAAGAGAC | 57690 |
rs755349720 | snp | A/G | 1.84538e-05 | 0.00303752 | missense | TNRC6C | GRCh38.p7 | 17:78049114 | CATACCAAGAAGACA[A/G]ATGGCAATAATGGCA | 57690 |
rs755356959 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053400 | TTTGGGAGGCCAAGG[A/C]GGGCAGATCATCTGA | 57690 |
rs755390405 | in-del | -/TGTAG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046001 | CCACAATTCAAAAAT[-/TGTAG]TGTTGTGTCACTTTC | 57690 |
rs755405044 | snp | A/G | 3.40223e-05 | 0.00412432 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093614 | TCATTTTGGTTTCTT[A/G]AACAGAATTCCATCC | 57690 |
rs755422105 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089883 | GGCTTGTTTCAGGGG[-/C]CCATTTTGCAAGGGC | 57690 |
rs755471269 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028675 | AATGTAAAGGGAAAC[-/A]GTACCGTATCATGAA | 57690 |
rs755474589 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020748 | ACAGAAAAATTGTTA[A/G]TGAGGTATTTCTCTT | 57690 |
rs755484171 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079957 | AGTATTGCTGAGGAT[A/G]TAAAAGAAACCCTTA | 57690 |
rs755489949 | snp | A/G | 1.71507e-05 | 0.00292832 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093138 | AGGTAAGACCATGCA[A/G]CACTTCTGTGCAACA | 57690 |
rs755491728 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046874 | AATTGAGTATGAACC[C/T]GTCAAATTGGGGGCT | 57690 |
rs755501445 | snp | C/G | 1.67517e-05 | 0.00289406 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064704 | ATTATTTTCTCTACC[C/G]CTTGGAACCTTTTTC | 57690 |
rs755509845 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065091 | CAGTGCCTCACACCT[A/G]TAATCCCAGCACTTT | 57690 |
rs755518368 | snp | A/G | 1.82537e-05 | 0.00302101 | missense | TNRC6C | GRCh38.p7 | 17:78050197 | ACCGTACAGCCTGGT[A/G]GTGAACACATGAACT | 57690 |
rs755521301 | snp | A/C | 1.66026e-05 | 0.00288115 | missense | TNRC6C | GRCh38.p7 | 17:78067869 | TGCTGCTTCCCAAGA[A/C]AGCACCTCCTCCTGC | 57690 |
rs755557295 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105440 | TGTCATTTTTTTATC[C/T]CAAAAAATATTTTTT | 57690 |
rs755582176 | snp | C/G | 1.66391e-05 | 0.00288431 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086556 | GGCCCAGCGTAATGT[C/G]TCCGGATCCATGAGA | 57690 |
rs755607788 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029676 | AGTTTTCACTCTTTC[A/T]TAATAACACTTAGCT | 57690 |
rs755611807 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017687 | GTGCTCTCCCAGCTA[C/T]AGGTCAAGTGATACA | 57690 |
rs755635633 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101758 | ATATCCTTAAGGCAC[A/G]GATCGCTCGTGCTAC | 57690 |
rs755665634 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051810 | CAAAGAAGATAGGAT[A/G]GACATGGTTCAGAAC | 57690 |
rs755666969 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076325 | ACGTGATCTGCCTCA[A/G]CTGCAGCTGTGGGGT | 57690 |
rs755708988 | snp | A/G | 1.70761e-05 | 0.00292194 | missense | TNRC6C | GRCh38.p7 | 17:78050051 | CAGGAGCTTGGGGCC[A/G]CCCCAGCCGAAGCAC | 57690 |
rs755712578 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031867 | ACATAGGATGAGACA[A/T]TGTTTTGATCTGAAA | 57690 |
rs755734413 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084733 | TTGTGGGTTCAAGCA[A/G]TTCTCCTGTCTCAGC | 57690 |
rs755761485 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071643 | TCTGCCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 57690 |
rs755791452 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074538 | CTGTGGAGTAGGACA[C/G]AGTTAGGGTGGGCCA | 57690 |
rs755800135 | snp | A/G | 1.65999e-05 | 0.00288091 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049932 | CAGTGCTGTGCAAAA[A/G]GAAGGAAGTGGAGGA | 57690 |
rs755810821 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093266 | TTGGCATTTTCCTTG[C/G]AAATCCATTTGTCAG | 57690 |
rs755835546 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008010 | AATATATGACATGCT[C/T]ATCTATGATACTCCT | 57690 |
rs755847008 | snp | A/G | 0.000104603 | 0.0072312 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077299 | GGTGGGATTGCCTCC[A/G]GGCTGGGCATGCAAA | 57690 |
rs755885046 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080175 | AATGTTGCCGGGCGC[A/G]GCGGCTCACGCCTGT | 57690 |
rs755894902 | snp | C/T | 6.7158e-05 | 0.00579435 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098524 | CCTCGGCTGGACCAG[C/T]TCCTACTCCTCGGGT | 57690 |
rs755921197 | in-del | -/AAAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092738 | GAAGTTGTCTCAAAA[-/AAAT]AAATAAATAAATAAA | 57690 |
rs755936899 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049587 | GTCTTTCAGCGCACA[A/G]CCTCAGAACCTTAAC | 57690 |
rs755936966 | snp | A/C | 1.67234e-05 | 0.00289161 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087114 | TGTCCCATGGTCTTC[A/C]ACAGCCACATCAGGT | 57690 |
rs755972642 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090444 | GCTCACTGTGCTTAC[A/G]TACCGTGTGGCGTAG | 57690 |
rs756012293 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036174 | AGTTCTTTCAGCTTC[A/G]CACACGAATTTCTGT | 57690 |
rs756022190 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020806 | AGTATATGTTTTAAT[A/G]CTAAGTACATCTCAA | 57690 |
rs756056008 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062254 | TATTGGTAACTATTT[A/G]CATAATATATTCCTC | 57690 |
rs756067258 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049551 | GAGCACAGAACCACA[A/G]ACGTCCACTTCTCAG | 57690 |
rs756076875 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092132 | TAACCATAGGAGGTA[A/T]TCTCACTCTCAAGCA | 57690 |
rs756079306 | in-del | -/C | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012254 | TAATTCATTAATTAA[-/C]TTAAACAGTTAATAA | 57690 |
rs756099059 | snp | G/T | 1.8237e-05 | 0.00301963 | missense | TNRC6C | GRCh38.p7 | 17:78050695 | TCGATAAGCTCTACT[G/T]CTGTTAGTACTGCTG | 57690 |
rs756130094 | snp | C/T | 3.32071e-05 | 0.00407461 | missense | TNRC6C | GRCh38.p7 | 17:78098418 | CTCTGTCTCATGAAC[C/T]ATGGAAGGTGCCCAG | 57690 |
rs756137670 | snp | C/T | 1.73123e-05 | 0.00294208 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064870 | GTGGGGAGATCACCC[C/T]GCAGAGCCGCCGGTG | 57690 |
rs756154633 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098728 | CCTGGTGTTTTTAGC[A/G]TCAGCCTAGGTGTGC | 57690 |
rs756171360 | snp | G/T | 1.82513e-05 | 0.00302082 | missense | TNRC6C | GRCh38.p7 | 17:78050212 | GGTGAACACATGAAC[G/T]CCTGGGCCAAAGCGG | 57690 |
rs756216336 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015145 | AAATGACTAGAATTA[C/G]TGCTTGATTTTTGAC | 57690 |
rs756270844 | snp | A/G | 0.000852152 | 0.020624 | missense | TNRC6C | GRCh38.p7 | 17:78104804 | CCCACGCCGCTAACC[A/G]CCCTGCTGCCTGGGG | 57690 |
rs756298903 | snp | A/G | 3.32336e-05 | 0.00407624 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064730 | TTTTCAGTTTCATCA[A/G]GCTGGGGAGAAATGC | 57690 |
rs756307098 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069367 | CTGCCATTTTTCATC[C/T]CTCAGACCCACAGAA | 57690 |
rs756325216 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081213 | GGCTCCTGATCACCT[C/G]CCAAAGGCCTCCGCT | 57690 |
rs756325366 | in-del | -/G | 7.67018e-05 | 0.00619234 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78051141 | GGAACAGGGTGGATC[-/G]GGGGGGCCGGTACCG | 57690 |
rs756359234 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038540 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 57690 |
rs756364971 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038099 | ACTACAGAAAGATGA[C/T]GTAAGAGAGTATTTT | 57690 |
rs756395093 | snp | C/G | 4.96874e-05 | 0.0049841 | missense | TNRC6C | GRCh38.p7 | 17:78079410 | ATACCGAGTGGCAAT[C/G]TGGGTATGTTTGGCA | 57690 |
rs756418139 | snp | C/G | 3.39265e-05 | 0.00411851 | missense | TNRC6C | GRCh38.p7 | 17:78049683 | AAATGGACTGCCAAA[C/G]TGGGGCATGGCTGTT | 57690 |
rs756421518 | snp | C/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105316 | GGTGTGGACCGCCGG[C/G]CGCAGAGCGGCTCCG | 57690 |
rs756442908 | snp | C/T | 1.93257e-05 | 0.00310845 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075137 | TTGTTGTGCTCCAGG[C/T]GCTCTGCTGGAAAAG | 57690 |
rs756478077 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033242 | GAATGTTACTGGTAT[A/C]TTCTTAGATAAGTAG | 57690 |
rs756496685 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063885 | CTTTTATGTCATTAC[A/G]TATAATACAAGATGT | 57690 |
rs756498054 | snp | C/T | 8.85125e-05 | 0.00665195 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78102490 | TTCTGCCTGGAGCAC[C/T]GACACCTCAGGAAGA | 57690 |
rs756534097 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096088 | AGCGCTGGGATTACA[C/T]GCGTGAGCCAGTGCG | 57690 |
rs756536640 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020693 | TTTAATAATGTTTAA[C/T]TTGATATATCCAAAA | 57690 |
rs756537625 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045570 | ACAAGTGCAGCTGAT[A/T]GGTGACTTCAGCTAG | 57690 |
rs756562489 | snp | A/C | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002381 | TCATAATCTCATTTA[A/C]AGCCAGGACATGTGG | 57690 |
rs756563973 | in-del | -/TTAGAAACTTTTTCTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056015 | TTTGATACGTGATCC[-/TTAGAAACTTTTTCTT]TTAGAGACAGAGTCT | 57690 |
rs756580200 | in-del | -/CTAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072945 | TCCAAAACCTAATAA[-/CTAT]GTCTTTAAGTTGATA | 57690 |
rs756602486 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031486 | GGTCTAGCTAAAGTT[C/T]TGGGTTCTTTTGCCT | 57690 |
rs756605219 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081609 | AGAAGCAGTGCAGGG[-/A]TCGGGGGTGACTCTG | 57690 |
rs756621476 | snp | C/T | 4.98956e-05 | 0.00499453 | missense | TNRC6C | GRCh38.p7 | 17:78086901 | ATCCAGCAGCACCAG[C/T]GCCAGCTGGCCCAGG | 57690 |
rs756658059 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044255 | AAGTTGGTTGCTAGT[C/T]AACATGGCAACCTAA | 57690 |
rs756661385 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089199 | TCTCAAACTCCTGAC[C/T]TCAAGTGATCCGCTC | 57690 |
rs756663962 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083220 | CGAGTGCAGATGCAC[A/G]GCACCTGCTGAGAGC | 57690 |
rs756712192 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087995 | TTGATTGCTATTAGA[A/G]TCTGTAGATACAGGA | 57690 |
rs756743890 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027022 | GATTTTGAAGTGTAT[C/G]AAGTATAAAAGAGTG | 57690 |
rs756746618 | snp | C/T | 3.43413e-05 | 0.0041436 | missense | TNRC6C | GRCh38.p7 | 17:78071163 | ACAGACATGGGCTTC[C/T]CGGTAACTGGCGTCG | 57690 |
rs756799476 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040145 | TGTAAATTCATGTAT[G/T]GATTTGGATGGGAGT | 57690 |
rs756829001 | snp | C/T | 1.65781e-05 | 0.00287902 | missense | TNRC6C | GRCh38.p7 | 17:78098451 | ACAGTACTGCACCCA[C/T]GAGGCCACCTCCAGG | 57690 |
rs756845920 | snp | G/T | 2.09883e-05 | 0.0032394 | missense | TNRC6C | GRCh38.p7 | 17:78049090 | AGTGCCCAGGGCAAC[G/T]TCACTGGACATACCA | 57690 |
rs756853474 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011036 | TCACATCTCTGTTTC[A/G]TATAACTTTTCACTA | 57690 |
rs756858366 | snp | G/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108991 | CTGGGACCACAGGCA[G/T]GCATGCGCCACCCCA | 57690 |
rs756899401 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095647 | GAACCTTGTTGCTCC[A/C]CTCTGGTACCTCTCT | 57690 |
rs756906352 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021545 | AAAGATTATGGAGAG[A/G]AGACATGGAATAGGT | 57690 |
rs756911691 | snp | A/C | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78048895 | AATTCCCACTGGGGA[A/C]AGCAGCCTACTTACA | 57690 |
rs756940705 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064959 | CTAGCATCCTGCTTG[C/T]CCTGATCTGGCAATT | 57690 |
rs756942543 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106403 | GTCAAGGTGACAGGC[G/T]TTGTGGCCACTGTCT | 57690 |
rs756943889 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102384 | TGACGGCCTGTGCTG[G/T]CCCACACTTCAGCAC | 57690 |
rs756979060 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090570 | TTCCAAACAAGCAGT[C/T]TGTCCTGCTCCAAAC | 57690 |
rs756983795 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094995 | AGCCAGAATCAGAGA[A/C]CCAGCCCTCCCCGCT | 57690 |
rs757001058 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018371 | CTGACCTCGTGATCC[A/G]CCCCGCCTCGGCCTC | 57690 |
rs757001130 | snp | A/G/T | 0.000552334 | 0.0166091 | missense | TNRC6C | GRCh38.p7 | 17:78104831 | GGGGACCTGCTCAGC[A/G/T]GGGAGTCCCTGTAGG | 57690 |
rs757043029 | in-del | -/CTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006576 | CCTTCTTCCTTCTTC[-/CTT]CTTCTTCCTTCTTCC | 57690 |
rs757074326 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005572 | TTGGTGGAAACACAC[A/G]CATTTCTCACTGTTA | 57690 |
rs757074586 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029556 | GAGGAGTCAGTGAGT[-/G]GGTGAGTGAATGTGA | 57690 |
rs757094412 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017515 | GTGCTTGTTGAGCTT[A/G]GGTAACCCATGACTG | 57690 |
rs757096496 | snp | C/T | 4.96816e-05 | 0.00498381 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079421 | CAATCTGGGTATGTT[C/T]GGCAATAGTGGAGCA | 57690 |
rs757118066 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028205 | CCGCTGAAACTTGGA[A/G]TTTTTACTTGATGGC | 57690 |
rs757191384 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100479 | GCTCCCTCTGAAGCC[A/G]TGGCCCAAACTGTAC | 57690 |
rs757200842 | snp | G/T | 0.000943129 | 0.021695 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073140 | TACCCAGCTGTGAAG[G/T]TTTACTTTCCAGAAG | 57690 |
rs757202314 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090616 | AAACTCTTTACTTCA[A/G]CCTTCTTTTCATTGT | 57690 |
rs757215089 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101669 | AGCATTGTTTCCGTA[A/G]ATACTAGATTAACTA | 57690 |
rs757237541 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037960 | ACACAGATCCAGGAA[-/C]CTATGATATAAAGAG | 57690 |
rs757241215 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059478 | TCCGTGGCGTGAGAC[C/G]TGTGAACCCCACATG | 57690 |
rs757249386 | snp | A/T | 1.71761e-05 | 0.00293049 | missense | TNRC6C | GRCh38.p7 | 17:78049702 | GGCATGGCTGTTGGT[A/T]TGGGGGCCATCATCC | 57690 |
rs757258259 | snp | C/G | 1.74278e-05 | 0.00295188 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091432 | CCTAACCGCATCTCT[C/G]TCTTTAGCTGGACTG | 57690 |
rs757266018 | snp | A/G | 1.65638e-05 | 0.00287778 | missense | TNRC6C | GRCh38.p7 | 17:78049607 | AGAACCTTAACACTG[A/G]TGGACCAAATAACAC | 57690 |
rs757350778 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024093 | GAGCAAAAAAAACAC[C/T]GTCTCAAAAAAAAGC | 57690 |
rs757369671 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096794 | TATTCCATCCTCGCT[C/G]TTCTTCTCCAGCTTC | 57690 |
rs757388769 | snp | G/T | 1.65908e-05 | 0.00288012 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093804 | TGCATGGACGGTCTC[G/T]CTAGACCCATTTGGA | 57690 |
rs757407188 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037166 | AGTGTACTGGCTTCA[C/T]ACTTTTTCACTCTTT | 57690 |
rs757415783 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107770 | CTGGGACGGCAGCAA[C/G]AAGATGCCGGGGCTT | 57690 |
rs757418521 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108777 | CTTCACCTGCATCTG[C/T]GGATATATATTTTTT | 57690 |
rs757440701 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080027 | AAATGTGATCTCATA[C/T]AATAGTGTATATATT | 57690 |
rs757452762 | snp | C/T | 1.76067e-05 | 0.00296699 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067711 | TGGAAGCATTGTCTG[C/T]GTTAGGGACATGAAT | 57690 |
rs757452785 | snp | C/T | 1.7413e-05 | 0.00295062 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050346 | TAAAGGGATTATAGA[C/T]CAAGGGCACATCCAG | 57690 |
rs757468077 | snp | C/T | 1.65721e-05 | 0.0028785 | missense | TNRC6C | GRCh38.p7 | 17:78093688 | GACCCTGACGTCACT[C/T]CTGGCAGTGTCCCCA | 57690 |
rs757481922 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068417 | TCATGTCAACAGAAG[-/T]TCTTTGGGATCTTCA | 57690 |
rs757503005 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074457 | TAATCGTGCACGTGC[A/G]ACAACGTGTGGTGCA | 57690 |
rs757523148 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045367 | CACTTCAGCTATTGG[G/T]GATGGATATTGGCCT | 57690 |
rs757602515 | snp | C/G | 3.36553e-05 | 0.00410201 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104468 | CCCTGTTCACGTGCC[C/G]CATCTTGCTGTTGCA | 57690 |
rs757608746 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002271 | ATACCAGAAATTGGT[A/G]CCAGAAATGCCCTGA | 57690 |
rs757626850 | snp | A/G | 1.65806e-05 | 0.00287924 | missense | TNRC6C | GRCh38.p7 | 17:78103493 | ATCTGACTCAAGGCA[A/G]TGCTGTGGTCCGGTA | 57690 |
rs757674894 | snp | G/T | 1.86003e-05 | 0.00304956 | missense | TNRC6C | GRCh38.p7 | 17:78051027 | TCCAGGTACAAACTG[G/T]GGGGAGACTTTAAAA | 57690 |
rs757678769 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031096 | ACAGAGTGAGACACT[A/G]TCTCACACTTAAAAA | 57690 |
rs757697783 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086424 | TTTTTTTATTTTTTA[A/G]CTAATGTCAGAAAGT | 57690 |
rs757703559 | snp | C/T | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031759 | CCAGTGTGAGCCCAA[C/T]CCAGGGTGCTGGGCC | 57690 |
rs757733689 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044130 | TTTCAACATAGATTC[A/T]TAGTCTCAGTTGTAA | 57690 |
rs757770144 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069091 | ATGTAAAAACTGTAC[A/G]TGACAGAAAATACCA | 57690 |
rs757777484 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094911 | GTTACGGGTGTCCCT[A/G]CTGTCAGACACAGCC | 57690 |
rs757785094 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043126 | CAAGAGAGCAGCTGA[A/G]GTATGGAAAAAAAGG | 57690 |
rs757790242 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055174 | AAACACACATTGTAC[A/T]GCTTCACAAAAGTAT | 57690 |
rs757797520 | snp | C/T | 6.9627e-05 | 0.00589988 | missense | TNRC6C | GRCh38.p7 | 17:78049718 | TGGGGGCCATCATCC[C/T]GCCCCACCTGCAAGG | 57690 |
rs757812159 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009841 | TACAGGCGTGAGCCA[C/T]TGCCCCTGGCCTGAA | 57690 |
rs757875444 | snp | C/T | 3.18608e-05 | 0.00399117 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102468 | GGTTCTCCCCTCTTG[C/T]TGCAGGTTCTGCCTG | 57690 |
rs757899185 | snp | C/T | 2.15515e-05 | 0.00328257 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075188 | TGGGCTGGGAGTGAC[C/T]GACCATAATGGAATG | 57690 |
rs757921692 | snp | C/T | 2.01359e-05 | 0.00317294 | missense | TNRC6C | GRCh38.p7 | 17:78091563 | ACTCCATGGATAACT[C/T]GCCCAGTGCCGCTTC | 57690 |
rs757945649 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008581 | CCTTGATTTTCCTCT[A/G]TGCCTCTAAGTCTGC | 57690 |
rs757966349 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052103 | CACTTCATCCATCTC[A/G]TGAAGCAAGGAGCAG | 57690 |
rs758000734 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019603 | CAAAAGGCAAAAGCT[C/T]ACTAGGCAAAGAGTA | 57690 |
rs758054966 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058888 | TGCTTTAAAACTTAG[-/T]TTTCTGAAACAATTA | 57690 |
rs758056995 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033124 | CTTATTTTGAAAAAC[G/T]GAATAAGAAATGTAA | 57690 |
rs758067341 | snp | A/G | 1.75533e-05 | 0.00296249 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067719 | TTGTCTGCGTTAGGG[A/G]CATGAATTTGATAAG | 57690 |
rs758073918 | in-del | -/GTGA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054246 | TGGAAGTGGCTGTGG[-/GTGA]GTCAGTGAGTTAGTG | 57690 |
rs758074491 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062636 | GCTTATGGCAGAAGC[A/G]AAAGATTAGAATTTG | 57690 |
rs758102907 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075319 | TTTGCTTTTTTAACA[A/G]GAGGAGTTTTTCATT | 57690 |
rs758110617 | snp | A/G | 0.00012851 | 0.00801489 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097701 | TAGAGTCATGAACCC[A/G]GACACCGCCACCACC | 57690 |
rs758134531 | snp | C/G | 5.0647e-05 | 0.00503199 | missense | TNRC6C | GRCh38.p7 | 17:78049211 | ATGGAAGTGCGGCCA[C/G]AGTGTGGGGTGTAGC | 57690 |
rs758146650 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069009 | AACAATTTTGGACTC[-/A]AGAGAGGCCTAACTA | 57690 |
rs758220359 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042446 | TAAGGGTCAGCTAAG[C/T]CGACGTGTATGGAAA | 57690 |
rs758226917 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025558 | AAACATTTGTGTGCA[A/G]GTTTTTGTATGAACG | 57690 |
rs758256697 | snp | A/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105238 | AGACGTGAAGCCTAT[A/T]TAAAATGAGCCTGTG | 57690 |
rs758259617 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095596 | AGTTCATGTGGCTCA[C/T]GCCAGGCCTCCCCTT | 57690 |
rs758262097 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026868 | AAATAGATGGGTGAA[A/T]TTGAGGGATATTTGA | 57690 |
rs758293972 | snp | A/G | 3.31796e-05 | 0.00407292 | missense | TNRC6C | GRCh38.p7 | 17:78083093 | AAAACATTGGTCTCA[A/G]CCCTGCACTATTAAC | 57690 |
rs758324480 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071391 | ATTTCTATCAAAAAG[A/G]GTGTGAGAGCCTTTT | 57690 |
rs758329456 | snp | C/T | 1.97748e-05 | 0.00314436 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064899 | TGGCATTTGGAAGAG[C/T]TGGCGCACCTGTTGC | 57690 |
rs758342411 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053108 | CCCCCCGACCCCTGA[C/T]GGTTCCCAACACTGA | 57690 |
rs758356359 | snp | C/T | 5.21853e-05 | 0.00510783 | missense | TNRC6C | GRCh38.p7 | 17:78049805 | GAATAAGCAATTCTG[C/T]GTGGGGACTGTCCCC | 57690 |
rs758375785 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070344 | TGCTCCATGATATAG[C/T]TGTGGCAGGCTCAAT | 57690 |
rs758392597 | in-del | -/TA | 0.000225587 | 0.010618 | intron-variant | TNRC6C | GRCh38.p7 | 17:78082999 | ACAGGTACAAGTAAC[-/TA]TTTTAACAGAGATAC | 57690 |
rs758415109 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070630 | TAAAATTAACAGGTT[A/G]TTTCATCCTTTCTTC | 57690 |
rs758417127 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038700 | AAAAAAAAAAAAAAG[G/T]ATTTCCTTGTAATCA | 57690 |
rs758424537 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034471 | TTGCTGCCCCCCCAA[-/C]CCCCACTTTACTTCC | 57690 |
rs758431420 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082215 | CCTTCTGATCCTGTG[A/G]TGCCACCAATGCACT | 57690 |
rs758453715 | snp | C/T | 3.57622e-05 | 0.00422845 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091629 | CTGAGCTAGGATGCC[C/T]GTGGTGGGATCACTG | 57690 |
rs758461440 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021981 | GATAGTCTAATATTA[C/G]AAGTAGTTGGAACTC | 57690 |
rs758467397 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028744 | CTTCTACATAAAAGG[-/T]TATGTACAGAACTAG | 57690 |
rs758472311 | snp | C/T | 1.66247e-05 | 0.00288307 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079578 | GACTGAGCAACAGGA[C/T]ATAGATGCCAGTGTT | 57690 |
rs758498661 | snp | G/T | 0.000299513 | 0.0122338 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075304 | AGGTGGTTTGTTGTT[G/T]TTGCTTTTTTAACAA | 57690 |
rs758503600 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047026 | AATGCATTGGTCAGC[C/G]AGGTTGTTAACCCCC | 57690 |
rs758522535 | snp | A/G | 4.96857e-05 | 0.00498401 | missense | TNRC6C | GRCh38.p7 | 17:78087027 | CACCCACAGACTCCC[A/G]GCCTACCTGACCTGC | 57690 |
rs758542586 | snp | C/G/T | 5.73115e-05 | 0.0053528 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049104 | CTTCACTGGACATAC[C/G/T]AAGAAGACAAATGGC | 57690 |
rs758550364 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059428 | GGAGTTGGGAGCCTG[C/G]TACGGAAGTAGGAAG | 57690 |
rs758584879 | snp | A/G | 3.32016e-05 | 0.00407427 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086957 | GCCACCGCCCCCGCC[A/G]CACCTGTCTCTGCAC | 57690 |
rs758595348 | snp | C/T | 3.32602e-05 | 0.00407786 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049374 | CCTTAATCCTAATGC[C/T]AACCCAGCTGCCTGG | 57690 |
rs758613764 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090506 | ATGTGGTAAGGGGAA[C/T]TGCAGCTGGAAATAC | 57690 |
rs758621340 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084992 | AGGAATCGCTGTGGG[A/G]AGGCAGTGCACATGT | 57690 |
rs758632647 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017382 | ATAGGGAACTTCTTT[C/T]CCCATGTTGCATTCC | 57690 |
rs758662607 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101562 | AGAAATAGAGCGGTG[G/T]GAAGTGGGAAATCGG | 57690 |
rs758701446 | snp | A/G | 3.4125e-05 | 0.00413054 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093133 | CCCCCAGGTAAGACC[A/G]TGCAACACTTCTGTG | 57690 |
rs758701916 | snp | A/G | 1.86287e-05 | 0.00305189 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086477 | CTTAATTATCATACT[A/G]TTTTAACTCTTCGTT | 57690 |
rs758711472 | snp | A/T | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012512 | AGGCTTTTTTAAAAA[A/T]GTTCCCTGTTCTCAA | 57690 |
rs758793532 | snp | A/G | 3.31912e-05 | 0.00407363 | missense | TNRC6C | GRCh38.p7 | 17:78093056 | CCGTAGCTGTTCCCC[A/G]TAGCTGGTCACGTGC | 57690 |
rs758799290 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004805 | ACAGTATACCTATTA[A/G]AGCCTGTTAAAATTA | 57690 |
rs758807268 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067050 | TGAAGCATCCCATAT[A/G]CAAATTTTCCTGCCA | 57690 |
rs758811461 | snp | G/T | 1.66286e-05 | 0.0028834 | missense | TNRC6C | GRCh38.p7 | 17:78049975 | TCAGGACCTCCTGCT[G/T]GTCCTGGAATACTCG | 57690 |
rs758823046 | snp | A/G | 0.000138591 | 0.00832322 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104629 | GCGGCTCAGCGCAGC[A/G]GGCAGCTCCCATGGC | 57690 |
rs758834617 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023163 | AACATAACGTATGCG[A/G]GAGGATATGCGTAGG | 57690 |
rs758839243 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066226 | ACAGAGACTCCATCT[-/C]AAAAAAAAAAAAAAA | 57690 |
rs758874662 | snp | A/G | 6.23928e-05 | 0.00558502 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104497 | CAGGTGCGTCCTGGG[A/G]AACACTACCATCCTG | 57690 |
rs758883018 | snp | C/T | 3.39426e-05 | 0.00411948 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077233 | CCGTTCTTGCCTTCC[C/T]CAAGCCTGAAGCTCC | 57690 |
rs758902897 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041526 | TTATTCTTTTGGACA[C/T]TATTTGTGTTTCCAA | 57690 |
rs758940164 | snp | C/T | 9.46656e-05 | 0.00687923 | missense | TNRC6C | GRCh38.p7 | 17:78051347 | CGACCAATACCACCA[C/T]CACCACCACCACTAC | 57690 |
rs759028039 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108632 | ACTGGGAACTCGGGG[A/G]ACAGGAGGGCAGCAC | 57690 |
rs759029168 | snp | C/T | 4.98368e-05 | 0.00499158 | missense | TNRC6C | GRCh38.p7 | 17:78093025 | ATCCAGAACAGTGAG[C/T]CACCAGCCAGTCCTC | 57690 |
rs759031482 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003250 | ATACAAAGCCCCTAA[C/T]TGGTATTTCAGTGCC | 57690 |
rs759044309 | snp | C/T | 0.000147272 | 0.00857987 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051177 | ACAGAAGGACAGCAG[C/T]GAAGCAACTGGCTGG | 57690 |
rs759133868 | snp | A/C/G | 3.32448e-05 | 0.00407695 | missense | TNRC6C | GRCh38.p7 | 17:78049426 | ACCGTGGCGACAGGC[A/C/G]ACCCTTCCAGTATTT | 57690 |
rs759141687 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088757 | AGGCATGAGCCATCA[C/T]ACCTGGCCTAATATG | 57690 |
rs759145601 | in-del | -/GTG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067206 | AAAAATTAGCTGGAT[-/GTG]GTGGTGGCACATGCC | 57690 |
rs759162939 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045153 | ATTATTGTGGGTGGG[A/G]CAGTAGGGGGCATGG | 57690 |
rs759166543 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014857 | GGCACCACTTTGTAT[A/C]CCTCCAGGACTGCTG | 57690 |
rs759199779 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078160 | CTGTGTGATCCTGGC[A/G]ATCTGACATTGCCCC | 57690 |
rs759205577 | snp | C/T | 3.3749e-05 | 0.00410772 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077190 | CTCCAATCAGGATGG[C/T]GGCCTCGTGGAAGAG | 57690 |
rs759334342 | snp | A/G | 1.69873e-05 | 0.00291434 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086836 | CTAGTTAACGCACCT[A/G]TGTCTCTGCCTGCCA | 57690 |
rs759355904 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009581 | TTTTTTGAGATGGAG[G/T]TTTGCTCTTGTTGCC | 57690 |
rs759356131 | snp | C/T | 3.46644e-05 | 0.00416305 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067940 | TAAGTACAACACTCT[C/T]AACGACGGTACACCC | 57690 |
rs759362562 | in-del | -/CA | 0.000422751 | 0.0145326 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78050032 | GGCGTTGGTAATATC[-/CA]TTCAGGAGCTTGGGG | 57690 |
rs759376344 | snp | C/T | 4.77316e-05 | 0.00488503 | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049041 | TGACTCTGCCTCCAA[C/T]TGTGGCTCAGAGAAC | 57690 |
rs759381720 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106181 | GGGGGAGCCTGGGGT[G/T]TGGGCTCCCACCTGT | 57690 |
rs759406405 | snp | C/T | 0.000130319 | 0.00807108 | missense | TNRC6C | GRCh38.p7 | 17:78051434 | AGCTGAATCGATCAC[C/T]GTTGCTTGGTCCAGG | 57690 |
rs759416869 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064434 | CAGTGACACGCCCCA[C/G]TAGTCCCAGCTACTT | 57690 |
rs759459196 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020494 | CACTTTCAGTCTTTA[C/T]GAAAACAGGTAATTA | 57690 |
rs759461313 | snp | C/T | 3.33957e-05 | 0.00408616 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093102 | TAAAATCTCAAATGG[C/T]TCTAGCATCAACTGG | 57690 |
rs759486583 | snp | C/T | 1.69043e-05 | 0.00290721 | missense | TNRC6C | GRCh38.p7 | 17:78050030 | ATGGCGTTGGTAATA[C/T]CCATTCAGGAGCTTG | 57690 |
rs759525700 | snp | C/G | 1.66479e-05 | 0.00288508 | missense | TNRC6C | GRCh38.p7 | 17:78086526 | ACGTTTACAAATCCA[C/G]CAGCAGATGTTACAG | 57690 |
rs759547862 | snp | A/G | 8.39863e-05 | 0.00647967 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091495 | GACCGGTGGCTTGTC[A/G]GTGAAGGACCCATCC | 57690 |
rs759578064 | snp | A/G/T | 3.34561e-05 | 0.00408989 | missense | TNRC6C | GRCh38.p7 | 17:78049660 | AACCCTATCAATGCA[A/G/T]TGCAGACAAATGGAC | 57690 |
rs759637971 | snp | A/G | 1.77181e-05 | 0.00297636 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098584 | GGCCTTACCCTTTAG[A/G]GGATGTGCTTATCAC | 57690 |
rs759654551 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029190 | GGCAGTGCTACAGAC[A/G]CCAAACCACAGTTGC | 57690 |
rs759656802 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017280 | AGTTATGACTTGGGT[G/T]ATTGAATAAGATAGA | 57690 |
rs759666081 | snp | C/G/T | 5.28549e-05 | 0.00514054 | missense | TNRC6C | GRCh38.p7 | 17:78050785 | ACCTGGGGTGAGCCT[C/G/T]CAAAGCCCAAATCCC | 57690 |
rs759709773 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027807 | GATGTGCGTCTTTGA[C/G]TTGATGGAATACAGT | 57690 |
rs759726065 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059115 | CTAGGAAGTTTATCA[C/T]TCTTTAGTATAAAAA | 57690 |
rs759729541 | snp | C/T | 3.32022e-05 | 0.00407431 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050913 | GAAAAAAAATGGATC[C/T]GGATGGGATGCTGAC | 57690 |
rs759734322 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040938 | GCCCGCGGGTGGCCC[G/T]GACGCAGACTGGCCC | 57690 |
rs759780026 | snp | A/C | 0.000470178 | 0.0153254 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064943 | TGCAAACCAGGTAAG[A/C]CTAGCATCCTGCTTG | 57690 |
rs759799109 | snp | A/C | 3.335e-05 | 0.00408337 | missense | TNRC6C | GRCh38.p7 | 17:78098510 | TGGGGTGCCAGCCCC[A/C]TCGGCTGGACCAGCT | 57690 |
rs759807792 | snp | A/G | 1.82231e-05 | 0.00301848 | missense | TNRC6C | GRCh38.p7 | 17:78050668 | CCAAGTGGCCCGGGG[A/G]TTTGGGGGGACTCGA | 57690 |
rs759817758 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011697 | ATCTTGAGTAAATGT[A/G]TAATAGTAAAATGGC | 57690 |
rs759843330 | snp | A/G | 7.8064e-05 | 0.00624707 | missense | TNRC6C | GRCh38.p7 | 17:78071085 | CACACTTTGTTCAAG[A/G]GCATGAAGACGTCTG | 57690 |
rs759862594 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107125 | GAGCATGCGTGTGCG[-/T]TATGTGCGTCCGACA | 57690 |
rs759865564 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082815 | GGGGAAGCACATCAC[A/G]CGCTGTTGGCTCATT | 57690 |
rs759867693 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096019 | TTGGGCCACTGCACT[C/G]CAGCCTGGGTGACAG | 57690 |
rs759883504 | snp | A/G | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108111 | GGCCTCTGAAGACAA[A/G]CCGAGCACCCCAGCG | 57690 |
rs759929658 | snp | A/G | 1.68502e-05 | 0.00290255 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083029 | ACAACGGCTAATAGT[A/G]TATTTTATGTTAAAC | 57690 |
rs759937474 | snp | C/G | 1.80237e-05 | 0.00300192 | missense | TNRC6C | GRCh38.p7 | 17:78050314 | AGGGAAGGAACGGGA[C/G]AAGGCCGAAGGCGAG | 57690 |
rs759942763 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022987 | AGTAATCTAGAGATT[A/G]TTTAAATATATAGGA | 57690 |
rs759991038 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106942 | AGCTGGTTTTATAGA[G/T]GATCATGAACTATGC | 57690 |
rs759999560 | snp | C/T | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78048968 | GGACTGACAAGGAGG[C/T]GTGGCCTTCCATCAC | 57690 |
rs760005916 | in-del | -/T | 1.72919e-05 | 0.00294035 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067938 | GTAAGTACAACACTC[-/T]TTAACGACGGTACAC | 57690 |
rs760011302 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005211 | AAACTATTTTTTATT[A/G]TTCATTGTGAAATTC | 57690 |
rs760027222 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083853 | CTTACTGATTTTACT[A/G]TAATTGCCATGTCAT | 57690 |
rs760045088 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061750 | GTAAGCAAGTGTTCT[C/T]CCATTTCTAAGATTT | 57690 |
rs760093730 | in-del | -/T | 0.000259437 | 0.0113864 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098331 | TATGCTCCATCTCTC[-/T]TGCCTTTCTAGGTAA | 57690 |
rs760097716 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013538 | GTGCTGATTGCTATG[A/G]GAAGAAAATGTTAAA | 57690 |
rs760114591 | snp | A/G | 1.76434e-05 | 0.00297008 | missense | TNRC6C | GRCh38.p7 | 17:78049741 | CTGCAAGGCCTTCCT[A/G]GTGCTAATGGATCAT | 57690 |
rs760116366 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086061 | CCATGGCTGGGCGCC[A/G]TGGCTCATGCCTGTA | 57690 |
rs760133959 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013219 | CTTTAGATCTTCTGG[A/T]CCAGAGAGGGAGCCA | 57690 |
rs760172112 | snp | C/T | 0.000950119 | 0.0217751 | missense | TNRC6C | GRCh38.p7 | 17:78104793 | TGATAGGCAGCCCCA[C/T]GCCGCTAACCACCCT | 57690 |
rs760189283 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023880 | TTTGAAAGGCCAGGG[G/T]GGGTGGATCACCTAT | 57690 |
rs760192884 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006989 | TGGGGTTACAGGCAC[A/G]CATGGCCACACCCAG | 57690 |
rs760214814 | in-del | -/AC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029810 | ATTAAAAACCTAGAC[-/AC]ACACACACACACACA | 57690 |
rs760221085 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043929 | GAACAGTATTCCATT[C/G]TGTATATCTGCCATA | 57690 |
rs760261918 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024995 | GACGGGGTTTCACCA[C/T]GTTAGCCAGTGTGAT | 57690 |
rs760275877 | snp | C/T | 1.82158e-05 | 0.00301787 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050178 | TGTCACCAGCCAGAA[C/T]CCTACCGTACAGCCT | 57690 |
rs760282848 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010136 | CACTTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 57690 |
rs760299122 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055712 | CTACAGAGGGCCCTA[C/T]GCCTGGCACTGGAGT | 57690 |
rs760312274 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097446 | TGGTCCTTTAAAACT[C/T]TTAAAACATGGTATT | 57690 |
rs760357110 | snp | C/T | 1.83448e-05 | 0.00302854 | missense | TNRC6C | GRCh38.p7 | 17:78104613 | GCGCGTCCAGCCAGC[C/T]GCGGCTCAGCGCAGC | 57690 |
rs760366075 | snp | A/C | 9.8227e-05 | 0.00700741 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051492 | AAGTAAAAAAAAAAA[A/C]AAAAAAGCTTATTCT | 57690 |
rs760368686 | in-del | -/GAACCCTACCGTACAGCCTGGTGGTGAACACAT | 1.81889e-05 | 0.00301565 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050175 | TAGTGTCACCAGCCA[lengthTooLong]GAACTCCTGGGCCAA | 57690 |
rs760404786 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099665 | CAATTCAAGATGAGA[C/T]TTGGGTGGGGACACA | 57690 |
rs760413543 | snp | A/G | 2.84224e-05 | 0.00376967 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077412 | TTGAGACATAAACTT[A/G]CTTATTTATAGTTAA | 57690 |
rs760433118 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020365 | GTGGCATTTTTTTCT[C/G]TTTGTAAAATAATGT | 57690 |
rs760441273 | in-del | -/CA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066226 | ACAGAGACTCCATCT[-/CA]AAAAAAAAAAAAAAA | 57690 |
rs760443242 | in-del | -/TAGGTCTAGCCTTTGGGCCAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022021 | CTGGCTCTTTTCCTG[-/TAGGTCTAGCCTTTGGGCCAA]AAAGATGCCCAGAGG | 57690 |
rs760464780 | in-del | -/TGAC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035658 | AATAGTCAAAATTTT[-/TGAC]TGACTAAATTCTAAA | 57690 |
rs760466603 | in-del | -/AAAA | 0.0618675 | 0.16464 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051481 | TGTTTCTTTACAAGT[-/AAAA]AAAAAAAAAAAAAAG | 57690 |
rs760467215 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045045 | GCACAGAGCAGGAGA[A/C]AGAATGATATGAATG | 57690 |
rs760486043 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019229 | AAAGGCTCAGACCCT[A/G]GCAAGGGTAGACTGG | 57690 |
rs760509738 | snp | A/G | 1.70275e-05 | 0.00291778 | missense | TNRC6C | GRCh38.p7 | 17:78050809 | AAATCCCAACACTGG[A/G]GAGATGGACAAAGAT | 57690 |
rs760540682 | snp | A/G | 1.81513e-05 | 0.00301253 | missense | TNRC6C | GRCh38.p7 | 17:78050290 | AACCACAATGAAGGA[A/G]GCACTGGGAGGGAAG | 57690 |
rs760585800 | snp | A/G | 1.67959e-05 | 0.00289787 | missense | TNRC6C | GRCh38.p7 | 17:78086853 | GTCTCTGCCTGCCAG[A/G]TTGCGCGCACAATCA | 57690 |
rs760622960 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051597 | ACCGTGCAATATTGT[A/G]TCTAAAGATTATCCA | 57690 |
rs760629345 | snp | C/T | 2.43176e-05 | 0.00348686 | missense | TNRC6C | GRCh38.p7 | 17:78049079 | TGGCTACAGGGAGTG[C/T]CCAGGGCAACTTCAC | 57690 |
rs760667375 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026547 | AAATGTGCCCTAGAA[C/T]TGATGAAATGTGGTG | 57690 |
rs760673149 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103684 | CCACCCTCCCACTTC[G/T]GGAGGCTGGAAGTCT | 57690 |
rs760690114 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018127 | TTTTTGGTTTTTGTT[C/T]TGTTTTTTTGGTTTT | 57690 |
rs760704740 | snp | A/G | 1.66034e-05 | 0.00288122 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083064 | TCAAGCACAGCTTTT[A/G]CAGTTTGCAGCAAAA | 57690 |
rs760772878 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095130 | GGAAGTTGGAAAGAA[C/T]CGAAGTTGCATGGCA | 57690 |
rs760812960 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070064 | AAAAATATAGTTTAT[A/G]AAAGCATTCAGTTAA | 57690 |
rs760869039 | snp | C/T | 3.62404e-05 | 0.00425663 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102558 | AGGTGCAATATGGTG[C/T]CCCTGCATCACTGAG | 57690 |
rs760889574 | snp | A/G | 1.66635e-05 | 0.00288643 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049854 | AAATAGCAATTCTGG[A/G]TTCAGTCAGGGGAAT | 57690 |
rs760897567 | in-del | -/GAA | 6.97229e-05 | 0.00590394 | cds-indel | TNRC6C | GRCh38.p7 | 17:78104528 | GCCGAGTTCGCTGGT[-/GAA]GAAGAAGTGAATCGC | 57690 |
rs760931296 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081896 | AGGACACAGAACCTT[G/T]GAAAGTTCATTTATA | 57690 |
rs760936133 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048689 | ATGGGATCTATTAAG[A/G]AGACAAATAGCTTTT | 57690 |
rs760941111 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052739 | GGGCCCTCCAGCCTC[C/T]TCGTAGACTTCTTGG | 57690 |
rs760955984 | snp | G/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002680 | GGAGGATCACTTGAG[G/T]CCAGGAGTTCGAGAC | 57690 |
rs760963864 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064223 | GCCTCAGCCTCCCCA[A/G]TAGCTCGGATTACAA | 57690 |
rs760972607 | snp | A/G | 0.000267953 | 0.0115717 | missense | TNRC6C | GRCh38.p7 | 17:78091478 | GTCAACAGCATGGAC[A/G]TGACCGGTGGCTTGT | 57690 |
rs760975811 | snp | A/G | 1.76702e-05 | 0.00297234 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049758 | TGCTAATGGATCATC[A/G]GTTTCTCAAGTCAGT | 57690 |
rs760989909 | snp | A/G | 1.69281e-05 | 0.00290925 | missense | TNRC6C | GRCh38.p7 | 17:78050556 | CGATGGGTCCATCAT[A/G]AACAGTACAAATACC | 57690 |
rs760991580 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094379 | GTTCCCAAAACATTG[A/T]ATTTCCCACTTGAAA | 57690 |
rs760992503 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051866 | TCAGTTCACTGACAT[A/G]CCCATGAGCACAGCA | 57690 |
rs760994758 | snp | A/G | 1.65946e-05 | 0.00288046 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050943 | CAGTAATAGGTCAGG[A/G]TCTGGTTGGAATGAC | 57690 |
rs761022330 | snp | C/G | 1.71155e-05 | 0.00292531 | missense | TNRC6C | GRCh38.p7 | 17:78091519 | CCCATCCCAGTCCCA[C/G]TCACGCCTCCCCCAG | 57690 |
rs761053571 | snp | A/C | 1.6916e-05 | 0.00290822 | missense | TNRC6C | GRCh38.p7 | 17:78098388 | CCTCTGGCCCTACCT[A/C]CCACACGCAAGCCTC | 57690 |
rs761053618 | snp | C/T | 1.65638e-05 | 0.00287778 | missense | TNRC6C | GRCh38.p7 | 17:78087010 | TGGACAGCTTCCCCT[C/T]GCACCCACAGACTCC | 57690 |
rs761070960 | in-del | -/CACAGCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087868 | GCCAGTCAGGAGAGA[-/CACAGCT]CACATACCTGAAGAC | 57690 |
rs761089440 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034044 | TTCCCCGCCTACTCT[A/C]CATGGCCTACTTTTT | 57690 |
rs761092705 | in-del | -/C | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108251 | CCCGCCACAGGCTGG[-/C]CCCCCCCCCACCCAT | 57690 |
rs761121550 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058804 | CCACTGTGGGCTCCT[A/C]CAAGTCGGCAAAGGC | 57690 |
rs761144824 | snp | G/T | 1.66366e-05 | 0.0028841 | missense | TNRC6C | GRCh38.p7 | 17:78049325 | GTCAGAATTGCTGGG[G/T]TGCTTCCAACTCCAA | 57690 |
rs761149843 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067124 | GAGGCAGGAGGACTA[C/T]TTGAGCCCAAGAGTT | 57690 |
rs761176799 | snp | A/G | 0.00010773 | 0.00733847 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064963 | CATCCTGCTTGCCCT[A/G]ATCTGGCAATTTGGA | 57690 |
rs761180004 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081831 | AGGCATCTGTGTGCC[A/G]TCTCACTGTTTCTTC | 57690 |
rs761192082 | in-del | -/AAATGACTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064978 | GATCTGGCAATTTGG[-/AAATGACTC]AAAGTATTGAATTTT | 57690 |
rs761230756 | snp | A/C | 0.000116158 | 0.00762009 | missense | TNRC6C | GRCh38.p7 | 17:78050482 | GAAAGGAAAAATGAC[A/C]ATGGGACAGAGGCCT | 57690 |
rs761244192 | snp | C/G | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109189 | CACAGTGCCCAGCAG[C/G]TAGCAGTGTGGCGTG | 57690 |
rs761244815 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007085 | TGACCTCAAATGATT[C/T]CCCCCCACCTCGGCC | 57690 |
rs761376604 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023859 | TCATGCCTGTAATCC[C/G]AGCACTTTGAAAGGC | 57690 |
rs761380171 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103901 | AACTTAATTCCCGCC[A/T]TAAAGACCCCATCTC | 57690 |
rs761389135 | in-del | -/TTA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022904 | GCAGACCTTTTTTTC[-/TTA]TTATTCCATAAACAA | 57690 |
rs761410571 | snp | C/T | 1.65693e-05 | 0.00287826 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093759 | CTACCTCCTCAAGAG[C/T]GGAGGTGAGGGTGCT | 57690 |
rs761424980 | snp | C/T | 0.000152005 | 0.00871662 | missense | TNRC6C | GRCh38.p7 | 17:78049205 | ACAGTAATGGAAGTG[C/T]GGCCAGAGTGTGGGG | 57690 |
rs761429790 | snp | C/T | 1.67402e-05 | 0.00289306 | missense | TNRC6C | GRCh38.p7 | 17:78086859 | GCCTGCCAGGTTGCG[C/T]GCACAATCACTAATC | 57690 |
rs761434668 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022854 | ATAAATGGACAGTTG[A/C]ATCTGTACTGATGCA | 57690 |
rs761439660 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006221 | GGGAGTCCAGGTCTC[G/T]GAACCTCTAGACTAG | 57690 |
rs761448689 | snp | A/C | 1.65913e-05 | 0.00288017 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050457 | GGAATTTGAAGAATC[A/C]CCTAGGTCTGAAAGG | 57690 |
rs761451521 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066781 | CTAGTCTGTAAGCAT[C/T]TCCTGCGGGCTTGTT | 57690 |
rs761495518 | in-del | -/CTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080442 | CAAGAGCGGAAACTC[-/CTT]CTGAAAAAAAGAAAG | 57690 |
rs761511490 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079645 | AAAGTGAGAGCGGAG[C/T]TAATCCATGTTTAAG | 57690 |
rs761518152 | snp | C/T | 1.73438e-05 | 0.00294476 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093585 | AATGTGCCGGTGTTC[C/T]GATCTGTGGCTTCTC | 57690 |
rs761533707 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022896 | GTACATGTGCAGACC[-/T]TTTTTTCTTATTATT | 57690 |
rs761558789 | snp | A/G | 1.67089e-05 | 0.00289035 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064853 | CCCAGCAGTGGCAGC[A/G]GGTGGGGAGATCACC | 57690 |
rs761564894 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078774 | GTTTGAGACCAGCCA[A/G]GACAACATGGCAAAA | 57690 |
rs761564961 | snp | A/G | 1.7871e-05 | 0.00298918 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091540 | CCTCCCCCAGTGGAC[A/G]CACCCCAACTCCATG | 57690 |
rs761567961 | snp | A/G | 1.98065e-05 | 0.00314688 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104875 | AGCACCAGGAGAGCC[A/G]ACCCCTCCCGGGACC | 57690 |
rs761580763 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074122 | CTTTACTGCCTTCTT[A/G]AGCTTAGAAACATGA | 57690 |
rs761591420 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087348 | TCTTGAACTCCTGGG[-/C]CTCAAGCAATCCTCC | 57690 |
rs761593681 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030482 | CAGCATCACCACAAA[A/C]ACGTGAGTAATGTGT | 57690 |
rs761615230 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055367 | GAAGTACAGTAAAGA[C/T]ATAAACTGGTAACAT | 57690 |
rs761625005 | snp | C/T | 5.74416e-05 | 0.00535887 | missense | TNRC6C | GRCh38.p7 | 17:78051097 | AACAATGTGAGTAAC[C/T]GGGGAGGAGCTGCTT | 57690 |
rs761631544 | snp | A/G | 1.66023e-05 | 0.00288113 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050964 | TTGGAATGACACCAC[A/G]AGATCTGGGAACAGT | 57690 |
rs761632136 | snp | C/T | 1.66477e-05 | 0.00288506 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103594 | CGCTCCAAGTAGCTC[C/T]CCATCCCCCAGAGCA | 57690 |
rs761647104 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029583 | GTGAAGGCCTAGGAC[A/G]TGACTATACACTTAG | 57690 |
rs761674689 | snp | A/G | 3.36151e-05 | 0.00409957 | missense | TNRC6C | GRCh38.p7 | 17:78049273 | TCTGTCAGTGGTGGG[A/G]ATGGAAAAATGGACA | 57690 |
rs761712648 | snp | C/T | 7.27193e-05 | 0.00602946 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075221 | CGCCAAGCCCCTCGG[C/T]TGCCGCCCGCCAATC | 57690 |
rs761722224 | snp | A/G | 4.78137e-05 | 0.00488923 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102587 | AGCATGATCCAGGGA[A/G]GGTTCCCGCTTGGCC | 57690 |
rs761723078 | in-del | -/TACTA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054800 | CAGACTACTGTACAC[-/TACTA]TACACCACTGCAGAC | 57690 |
rs761773570 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097289 | CACCCCAGTCAGAAG[A/G]AATACTCAAATTTTT | 57690 |
rs761782430 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083262 | TAATGTTTGTCTTCA[C/T]GTCAGGGATGTCATT | 57690 |
rs761793211 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038037 | AGAAAATAGTGGTTC[A/T]GATCAATATCGAGTG | 57690 |
rs761802197 | snp | A/G | 2.10511e-05 | 0.00324424 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075097 | GCTCAGCACTCACTT[A/G]TTTTGTTTACAACAT | 57690 |
rs761823394 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054867 | CTGTACACTACCATA[C/T]ACCACTGCAGACTAC | 57690 |
rs761834053 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020153 | GAATTCCGCATTCCT[C/G]TGTCTGTTGCTTTGC | 57690 |
rs761841907 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084508 | GAAGGAGGGAAGGAC[A/G]TGTCCCAGAGACACA | 57690 |
rs761845327 | snp | C/T | 1.66261e-05 | 0.00288319 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067812 | TGAAATGAACCTCAG[C/T]ACCAGCCAGTGGGAG | 57690 |
rs761901871 | snp | A/G | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012966 | ACTGATATGAATGAG[A/G]TAAGTGCATACAAGA | 57690 |
rs761934338 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78075138 | TGTTGTGCTCCAGGC[A/G]CTCTGCTGGAAAAGA | 57690 |
rs761987005 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007762 | TTAGATTGCATAATA[C/T]ACTGAATCAATCAAC | 57690 |
rs762032912 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051677 | ATATTAAGCACACTC[A/G]GTAGAACATCAAGCG | 57690 |
rs762042011 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018982 | AGTGTTAGTAGGTAA[C/G]AGAGCTCATTGCTGT | 57690 |
rs762066496 | snp | C/T | 3.32154e-05 | 0.00407512 | missense | TNRC6C | GRCh38.p7 | 17:78092998 | GATGACTCCTATGGC[C/T]GGTACGATTTAATCC | 57690 |
rs762107211 | snp | A/G | 1.65883e-05 | 0.00287991 | missense | TNRC6C | GRCh38.p7 | 17:78049883 | ATGGAGACACTGTGA[A/G]CTCAGCATTAAGTGC | 57690 |
rs762110826 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074773 | CCGAAATGAGGAAGC[A/G]AGTCTTGCAGAAAAC | 57690 |
rs762119393 | in-del | -/GAT | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109037 | TTTTATTTTTGTAGA[-/GAT]GATAGGGTCTCACCA | 57690 |
rs762138144 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015982 | TTCGGCTGAAGAATA[C/T]AGAAACTACTCTAGC | 57690 |
rs762139041 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048008 | ATGGCATATAAAGTT[A/G]TTCTAGGGATCTCCA | 57690 |
rs762141263 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062162 | CTCCCAATATATATT[A/G]TTGTCTTTTGTGTAA | 57690 |
rs762149825 | snp | A/G | 1.6591e-05 | 0.00288015 | missense | TNRC6C | GRCh38.p7 | 17:78083078 | TGCAGTTTGCAGCAA[A/G]AAACATTGGTCTCAA | 57690 |
rs762167185 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025108 | TACATTATTATTAAC[C/T]AAATGCCACAGTTTA | 57690 |
rs762205700 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070889 | TATACCAACCTGCAA[A/G]TGTACCTTGATGCTT | 57690 |
rs762223472 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045334 | TCCTTATGGCATCCT[A/G]TATGGCCATCCTTAG | 57690 |
rs762264186 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026445 | CACTATTTTATGTAC[C/G]ACTAAGAAAAAAATT | 57690 |
rs762280684 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057835 | CATTTTTGTGTGTGT[G/T]TGTGTGTTGTTTTAA | 57690 |
rs762291512 | snp | A/G | 0.000109049 | 0.00738327 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050652 | CAGCAACAACAAAGC[A/G]CCAAGTGGCCCGGGG | 57690 |
rs762315573 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78039008 | GTTGGGTAATATGAC[A/G]TAGTACATCCTGCAG | 57690 |
rs762324130 | snp | C/G | 1.73372e-05 | 0.0029442 | missense | TNRC6C | GRCh38.p7 | 17:78050584 | ACCTCTTCAGTATCT[C/G]GGTGGGTCAACGCGC | 57690 |
rs762366692 | snp | A/G | 1.66203e-05 | 0.00288268 | missense | TNRC6C | GRCh38.p7 | 17:78049435 | ACAGGCAACCCTTCC[A/G]GTATTTGCAGTCCAG | 57690 |
rs762399665 | snp | A/G | 0.000132258 | 0.00813089 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075230 | CCTCGGCTGCCGCCC[A/G]CCAATCTCCAAAGAG | 57690 |
rs762405023 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098607 | CTTATCACTTTGTCC[C/T]GTACCTCCTTTGTAA | 57690 |
rs762445472 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046457 | TGCTGGGATTACAGG[C/T]GAGAGCCACTGCGCC | 57690 |
rs762494303 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077613 | CTGGCTAAAGTGATG[A/T]TGTGTTGCACAGTGG | 57690 |
rs762507955 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059846 | AGGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs762513681 | snp | C/T | 1.6649e-05 | 0.00288518 | missense | TNRC6C | GRCh38.p7 | 17:78103432 | GATGGTTCTACACTG[C/T]GGACATTGTGTTTGC | 57690 |
rs762519419 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034963 | AACAGGAAAAAATAA[A/G]TAACGTCTCTGAGCT | 57690 |
rs762520627 | snp | A/G | | | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064808 | CCTTCTACCCTGGTG[A/G]ATAATGGCACAGCAG | 57690 |
rs762547212 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089072 | TTCTGGATTCAAGCA[A/G]TTCTCCTGCCTCAGC | 57690 |
rs762583490 | snp | A/C | 0.000807768 | 0.0200806 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086945 | GCAGCCACCACCGCC[A/C]CCGCCCCCGCCGCAC | 57690 |
rs762591431 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078586 | CAAATAACCATATTC[A/G]TGTTGCTGTTGTGTG | 57690 |
rs762593967 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068654 | CAAAAACTAGCTGGG[C/T]GTGGTGGTGGGTGCC | 57690 |
rs762606617 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085937 | ACCAACATCATCACC[-/A]ACACTAAACAGGTAT | 57690 |
rs762639920 | snp | C/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003344 | GGGAAGAGGCATCCA[C/G]AGAAGGAAAAAAGAT | 57690 |
rs762646630 | snp | A/G | 4.97063e-05 | 0.00498505 | missense | TNRC6C | GRCh38.p7 | 17:78086994 | GCAGGCAAATCGGCC[A/G]TGGACAGCTTCCCCT | 57690 |
rs762674211 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090122 | AGGCGTTTTGTTAGG[C/T]CTGCGAAGTGTGTGT | 57690 |
rs762678100 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106924 | AGACTGCAGATCCAC[-/A]AAAGCTGGTTTTATA | 57690 |
rs762694421 | snp | C/T | 1.67778e-05 | 0.00289631 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049287 | GGATGGAAAAATGGA[C/T]ACTATGATTGGAGAT | 57690 |
rs762702292 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098967 | AGATGTCACTGGGAC[A/G]TAAGGCTTTTGCAGG | 57690 |
rs762730011 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042114 | CAACCATGCTATTAT[A/G]TAATCCTTTTTAATT | 57690 |
rs762761237 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073670 | ACCAGTGCTCCTAGG[A/G]GACATACAGGGTTGG | 57690 |
rs762769567 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096111 | CCAGTGCGCACGGCC[A/G]AGCTGACACCCTTTT | 57690 |
rs762772516 | snp | A/G | 1.66743e-05 | 0.00288736 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083195 | CCCATGCAAGTTAGA[A/G]CACGCAGGCCGAGTG | 57690 |
rs762787135 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054847 | CCATACACCACTGCA[A/G]ACTACTGTACACTAC | 57690 |
rs762829369 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107610 | TGAACTCAGATTTTC[C/T]ATTGTTTTGCTTTAT | 57690 |
rs762840151 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054089 | GCACAGCATATTACT[A/G]TACTGAATACTGTAG | 57690 |
rs762866999 | snp | A/G | 1.66034e-05 | 0.00288122 | missense | TNRC6C | GRCh38.p7 | 17:78093004 | TCCTATGGCCGGTAC[A/G]ATTTAATCCAGAACA | 57690 |
rs762881630 | snp | A/C | 3.46182e-05 | 0.00416028 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077165 | ACTGCACACAGCTCA[A/C]CCTTTCTTTCTCCAA | 57690 |
rs762881789 | snp | C/T | 7.00501e-05 | 0.00591778 | missense | TNRC6C | GRCh38.p7 | 17:78051131 | TGAAACAGACAGGAA[C/T]AGGGTGGATCGGGGG | 57690 |
rs762901338 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084220 | ACCTGGAAGGCGGAG[G/T]TTGCAGTGAGCCTCG | 57690 |
rs762917258 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018838 | AATCCAGGCCATAGA[C/T]TGAGAGAAGCTGGAT | 57690 |
rs762928361 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022725 | GCATTTTCTTCATTT[C/T]GAGTCTTTTAAAAGG | 57690 |
rs762965726 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065532 | CACACTACTTCAGCA[A/G]TATTCTTGTACCTGC | 57690 |
rs762968278 | in-del | -/AG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069251 | TAGAAAAAGGAGCAC[-/AG]AATGTGAAGAGTAGC | 57690 |
rs762969879 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095361 | CAACTTGCGGGGAGG[A/G]CAGAAGAGAACCTAA | 57690 |
rs763002626 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010898 | GAGTAGGTACATGAA[C/T]GTATAAGTTCTTGAA | 57690 |
rs763041039 | snp | C/T | 5.00463e-05 | 0.00500206 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098401 | CTCCCACACGCAAGC[C/T]TCTCTGTCTCATGAA | 57690 |
rs763052664 | snp | A/C | | | missense | TNRC6C | GRCh38.p7 | 17:78051161 | GGCCGGTACCGGTCA[A/C]ACAGAAGGACAGCAG | 57690 |
rs763064405 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026560 | AATTGATGAAATGTG[A/G]TGGTTAGATGAAGAA | 57690 |
rs763099439 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006670 | TGGTTTAGTACCAGC[G/T]ATATTCTTCATCATT | 57690 |
rs763139045 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091695 | GGCCATTCTATACTT[A/T]TCTAAGAATTGAGCA | 57690 |
rs763167366 | snp | A/G | 1.89863e-05 | 0.00308104 | missense | TNRC6C | GRCh38.p7 | 17:78104775 | GCGCCGACGACAGCA[A/G]GGTGATAGGCAGCCC | 57690 |
rs763189921 | snp | C/T | 1.65605e-05 | 0.0028775 | missense | TNRC6C | GRCh38.p7 | 17:78079485 | CCACCAGTGCAGCCT[C/T]TTAACTCTTCCCAGC | 57690 |
rs763190105 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060808 | AGCTATGTAAGTGGC[A/G]TCTGTGGAACAAGCT | 57690 |
rs763245868 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020113 | ATATAAAAGAGACCC[-/A]GAGGTGTACAGCTCA | 57690 |
rs763328509 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037967 | ATCCAGGAACTATGA[C/T]ATAAAGAGAGCAGGG | 57690 |
rs763328523 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023922 | CAAGACCAGCCTGGC[C/T]GACATGGTGAAACCC | 57690 |
rs763444005 | snp | C/T | 0.000109937 | 0.00741327 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049086 | AGGGAGTGCCCAGGG[C/T]AACTTCACTGGACAT | 57690 |
rs763447600 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065588 | TTTCACTGAGCAAGA[C/T]AGATAAAACATGTCA | 57690 |
rs763449210 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051630 | GAGAGCAAAGTAGGA[A/T]CCTCTGGTGGTTTTC | 57690 |
rs763460674 | snp | A/C | 1.65641e-05 | 0.00287781 | missense | TNRC6C | GRCh38.p7 | 17:78049558 | GAACCACAAACGTCC[A/C]CTTCTCAGAATGTGT | 57690 |
rs763492447 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080932 | ATAAAATTTAATTTA[A/G]ATGTGTTTAGTTTGT | 57690 |
rs763523719 | snp | C/T | 4.99521e-05 | 0.00499736 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086559 | CCAGCGTAATGTGTC[C/T]GGATCCATGAGACAA | 57690 |
rs763527282 | snp | C/T | 3.57136e-05 | 0.00422558 | missense | TNRC6C | GRCh38.p7 | 17:78050771 | AGGACAAGTCACCCA[C/T]CTGGGGTGAGCCTCC | 57690 |
rs763533162 | in-del | -/TTCACT | 1.80829e-05 | 0.00300684 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050309 | TGGGAGGGAAGGAAC[-/TTCACT]GGGAGAAGGCCGAAG | 57690 |
rs763563020 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107673 | ATTGAAATCTTAATC[A/C]TCATCGAGAGGCACA | 57690 |
rs763586372 | snp | A/G | 1.79483e-05 | 0.00299564 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091407 | AAGTCATTTAGAGGA[A/G]CAGGCGAATCCTAAC | 57690 |
rs763603959 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099697 | CCAAACCATATCATT[C/T]TGCCCCTGACCCCTC | 57690 |
rs763617499 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106308 | TCAGAATGCAGATGC[A/G]TTCCTTCAGAGCTCT | 57690 |
rs763617933 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007592 | CTTCCCTCCCCTGCT[A/C]CAGATTGTGTGTCTA | 57690 |
rs763631089 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101600 | ACAGCCTTCAGAGCT[A/G]AGAGCCCTAAACAGA | 57690 |
rs763651945 | snp | C/T | 1.67711e-05 | 0.00289573 | missense | TNRC6C | GRCh38.p7 | 17:78086857 | CTGCCTGCCAGGTTG[C/T]GCGCACAATCACTAA | 57690 |
rs763695416 | snp | C/T | 0.000151982 | 0.00871596 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093120 | TAGCATCAACTGGCC[C/T]CCAGGTAAGACCATG | 57690 |
rs763723143 | in-del | -/ACTAC | 1.80981e-05 | 0.00300811 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78050303 | AAGCACTGGGAGGGA[-/ACTAC]AGGAACGGGAGAAGG | 57690 |
rs763744679 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010326 | GTAAGTCAGTTGAAG[C/T]CATAGTCTTCCAGTA | 57690 |
rs763821383 | snp | C/T | 2.10697e-05 | 0.00324568 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075094 | TGTGCTCAGCACTCA[C/T]TTGTTTTGTTTACAA | 57690 |
rs763849906 | snp | A/G | 3.51933e-05 | 0.00419469 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102449 | CACGGGGCCTTGTCA[A/G]CCAGGTTCTCCCCTC | 57690 |
rs763851123 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077642 | GGTCTTCGGCTGCCG[C/G]ATGCATCCAGAGGTC | 57690 |
rs763857362 | snp | C/G | 1.70845e-05 | 0.00292267 | missense | TNRC6C | GRCh38.p7 | 17:78050053 | GGAGCTTGGGGCCAC[C/G]CCAGCCGAAGCACCT | 57690 |
rs763892277 | snp | C/T | 1.70694e-05 | 0.00292137 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064672 | ATTATATTTTTGCTT[C/T]TCTCTGATGCACTTT | 57690 |
rs763902486 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078802 | AAACCCCGTCTCTAC[-/T]AAAAACACAAAAATT | 57690 |
rs763915138 | snp | A/C | 1.70397e-05 | 0.00291883 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049689 | ACTGCCAAACTGGGG[A/C]ATGGCTGTTGGTATG | 57690 |
rs763943751 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072956 | ATAACTATGTCTTTA[A/G]GTTGATAGTGATTAA | 57690 |
rs763956511 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024853 | AGGCTGGAGTGCAAT[A/G]GTGCGATCTCAGCTC | 57690 |
rs763956847 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051719 | GGTGGCGGTGGTGGC[C/T]TGGGGTGGAGATGAT | 57690 |
rs763987220 | snp | C/G | | | intron-variant, utr-variant-5-prime | TNRC6C | GRCh38.p7 | 17:78041074 | GAGGCAGCTGTGCAC[C/G]CGAGGTGGCGTCTCC | 57690 |
rs764004159 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028175 | GCTGGGATTACAGGC[A/G]TGAGCCATCGCCCCC | 57690 |
rs764022793 | snp | C/T | 1.68301e-05 | 0.00290082 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098530 | CTGGACCAGCTCCTA[C/T]TCCTCGGGTAAGCTC | 57690 |
rs764042773 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054112 | TACTGTAGGCAGTTG[A/T]AGGACGATGGTAAGT | 57690 |
rs764047247 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011926 | ACTTTATTTTAATGT[A/G]CTTATTTGTCATCTT | 57690 |
rs764049322 | in-del | -/TTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022901 | TGTGCAGACCTTTTT[-/TTC]TTATTATTCCATAAA | 57690 |
rs764111692 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092789 | ACAGAATCCTAGACA[A/G]ACCAAGTCTTACAAT | 57690 |
rs764135485 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022758 | AAATGACAAGTAGAA[A/G]TACAAGTGTAGTTGG | 57690 |
rs764161570 | snp | A/G | 1.65982e-05 | 0.00288077 | missense | TNRC6C | GRCh38.p7 | 17:78083066 | AAGCACAGCTTTTGC[A/G]GTTTGCAGCAAAAAA | 57690 |
rs764173179 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78050524 | GCTACTCAGGCTTCA[A/G]ACTCAGGGGGGAAGA | 57690 |
rs764181448 | in-del | -/TTACTGC | 1.66051e-05 | 0.00288137 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071183 | AACTGGCGTCGTAGT[-/TTACTGC]TACCCACCATGCTTC | 57690 |
rs764185897 | in-del | -/CCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021651 | CTCGGCTCACTGCAA[-/CCT]CTGCCTCCCTGGCTC | 57690 |
rs764249851 | snp | A/C | 1.65836e-05 | 0.0028795 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079548 | TCCCCTCAGGTCAGA[A/C]CCACATCCAAGCAGG | 57690 |
rs764277480 | in-del | -/AGTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102255 | TGGGAAGATCCAAAA[-/AGTC]AGAGTCACCACGGGG | 57690 |
rs764302463 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056013 | CCTTTGATACGTGAT[A/C]CTTAGAAACTTTTTC | 57690 |
rs764305442 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006765 | TGTCCCACCACTTTA[C/T]GCAGAGCTATCATTT | 57690 |
rs764328133 | snp | C/G | 2.3287e-05 | 0.00341217 | missense | TNRC6C | GRCh38.p7 | 17:78091583 | AGTGCCGCTTCCCCC[C/G]TGGAGCAGAACCCTA | 57690 |
rs764379295 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017387 | GAACTTCTTTTCCCA[C/T]GTTGCATTCCTGCTC | 57690 |
rs764396082 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097729 | ACCTTGCTCAGTGCC[A/G]TGTTTGGTTCTGCAG | 57690 |
rs764398298 | snp | A/C | 1.66263e-05 | 0.00288321 | missense | TNRC6C | GRCh38.p7 | 17:78049334 | GCTGGGGTGCTTCCA[A/C]CTCCAATGCTGGCAT | 57690 |
rs764434281 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045161 | GGGTGGGGCAGTAGG[C/G]GGCATGGGAAGAGAC | 57690 |
rs764438023 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093325 | CATTTTTCTGTAAAC[C/G]CTTAGTTCAGCATGA | 57690 |
rs764464490 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060906 | GATGTGATGTGCTTA[A/G]CAATGTTCAGTGAGA | 57690 |
rs764464585 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074105 | ATTTCCTCTGTAAGG[C/T]GCTTTACTGCCTTCT | 57690 |
rs764470863 | snp | C/G | 1.76717e-05 | 0.00297247 | missense | TNRC6C | GRCh38.p7 | 17:78049763 | ATGGATCATCAGTTT[C/G]TCAAGTCAGTGGGGG | 57690 |
rs764495786 | in-del | -/CGA | 0.000572902 | 0.0169152 | cds-indel | TNRC6C | GRCh38.p7 | 17:78104764 | GGGCCCGCCCAGCGC[-/CGA]CGACAGCAGGGTGAT | 57690 |
rs764506955 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013602 | GTCTTATGAGGAATG[A/G]ACATAAATCTCAACC | 57690 |
rs764546730 | snp | C/T | 1.66543e-05 | 0.00288563 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087099 | TACCCTCTCGGTGAG[C/T]GTCCCATGGTCTTCA | 57690 |
rs764555016 | snp | A/G | 1.69415e-05 | 0.00291041 | missense | TNRC6C | GRCh38.p7 | 17:78050558 | ATGGGTCCATCATGA[A/G]CAGTACAAATACCTC | 57690 |
rs764566788 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087011 | GGACAGCTTCCCCTC[A/G]CACCCACAGACTCCC | 57690 |
rs764627784 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080973 | TGTCTTAGTCCATTT[G/T]GGCTGCTGTAACAAA | 57690 |
rs764631530 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052050 | GAGATGAGAATGAAT[A/G]AAGAGGGAAGAGATC | 57690 |
rs764633316 | snp | C/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105003 | TCCTTGCGAACTGTT[C/T]GCAAAACAGTGCGGG | 57690 |
rs764654792 | snp | G/T | 9.85173e-05 | 0.00701776 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097858 | TCCGCACCTAGTGTT[G/T]CAGGTACGCGCCTGG | 57690 |
rs764681744 | snp | A/G | 6.75402e-05 | 0.00581081 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049206 | CAGTAATGGAAGTGC[A/G]GCCAGAGTGTGGGGT | 57690 |
rs764684516 | snp | A/G | 9.9822e-05 | 0.00706407 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077191 | TCCAATCAGGATGGC[A/G]GCCTCGTGGAAGAGC | 57690 |
rs764689177 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037008 | TTCTTTATATAGAAT[A/G]TGCTTCCTAACGAGA | 57690 |
rs764710794 | snp | C/T | 2.06183e-05 | 0.00321072 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075112 | GTTTTGTTTACAACA[C/T]TGCTTCTGTTTGTTG | 57690 |
rs764727420 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071174 | CTTCCCGGTAACTGG[C/T]GTCGTAGTTTACTGC | 57690 |
rs764757345 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079353 | AAACAATGTTACTCT[A/G]ATGCCTGCCTTGGTA | 57690 |
rs764759573 | snp | A/G | 1.65701e-05 | 0.00287833 | missense | TNRC6C | GRCh38.p7 | 17:78093763 | CTCCTCAAGAGTGGA[A/G]GTGAGGGTGCTGCTC | 57690 |
rs764783096 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081922 | TTATAATTAAAATAT[A/T]TGGAGGATGAGATCT | 57690 |
rs764816545 | snp | C/T | 0.000131518 | 0.00810814 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102462 | CAACCAGGTTCTCCC[C/T]TCTTGTTGCAGGTTC | 57690 |
rs764833736 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099701 | ACCATATCATTCTGC[C/T]CCTGACCCCTCCCAA | 57690 |
rs764870608 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054140 | AGTATTTATATATCT[A/G]AACATGAAAAGGGGA | 57690 |
rs764880983 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014887 | GATGAGCACAGCAGA[C/T]GGACCCTCCGTACTC | 57690 |
rs764894116 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032882 | ATAGTCTTGGCTTTC[A/G]TCTGCTAACCACTTG | 57690 |
rs764933134 | snp | G/T | 3.31807e-05 | 0.00407299 | missense | TNRC6C | GRCh38.p7 | 17:78083084 | TTGCAGCAAAAAACA[G/T]TGGTCTCAACCCTGC | 57690 |
rs764949338 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045229 | TGAGGGTGCTTGGAA[A/C]AGGGGCAGTCAGAGG | 57690 |
rs764989372 | snp | C/T | 1.96419e-05 | 0.00313378 | missense | TNRC6C | GRCh38.p7 | 17:78049099 | GGCAACTTCACTGGA[C/T]ATACCAAGAAGACAA | 57690 |
rs765008062 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057383 | CAAACTTGTTAGACC[-/A]AGCTATTATTTGAGC | 57690 |
rs765022060 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039643 | TGGTTAATGCTGTGG[C/T]TGTTGTCAGGCAGCA | 57690 |
rs765033952 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009799 | ACCTCGTGATCTGCC[C/T]ACTTCGGCCTCCCAA | 57690 |
rs765074057 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082828 | ACGCGCTGTTGGCTC[A/C]TTCTGGCAGCCCAAC | 57690 |
rs765126881 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095291 | ACGTGACAGCTGTCC[G/T]CAAGCTCCACATGCA | 57690 |
rs765135192 | snp | A/G | 5.30969e-05 | 0.00515224 | missense | TNRC6C | GRCh38.p7 | 17:78091599 | TGGAGCAGAACCCTA[A/G]CAAGCATGGTACGTC | 57690 |
rs765205031 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064469 | GGATTGAGTGAGCCC[A/G]GGAGTTGAGGGCAGC | 57690 |
rs765220544 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053054 | GAGCCACTTGCCTTC[A/G]TAAGGGCCTGTGCAT | 57690 |
rs765237628 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046928 | TAGACCATTAACAAA[C/G]GGCAGATCATTTTAC | 57690 |
rs765257327 | snp | A/G | 1.66103e-05 | 0.00288182 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050973 | CACCACGAGATCTGG[A/G]AACAGTGGCTGGGGC | 57690 |
rs765272469 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102297 | AGGGGGTCTGCAGGG[A/C]CTGTGAGGTTTTGGT | 57690 |
rs765287772 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106215 | CAGACCTTTTTTTCT[A/C]CTTCAGACTTTAAAA | 57690 |
rs765293196 | snp | C/T | 5.25721e-05 | 0.00512672 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050592 | AGTATCTGGGTGGGT[C/T]AACGCGCCACCTGCC | 57690 |
rs765320926 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094880 | TTTGGATGCAGCTGC[A/G]TTTCGGAACAGGGAT | 57690 |
rs765325718 | snp | A/G | 1.6646e-05 | 0.00288491 | missense | TNRC6C | GRCh38.p7 | 17:78050516 | GTTGTGCAGCTACTC[A/G]GGCTTCAAACTCAGG | 57690 |
rs765326567 | snp | C/T | 0.00049675 | 0.0157523 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087026 | GCACCCACAGACTCC[C/T]GGCCTACCTGACCTG | 57690 |
rs765329954 | in-del | -/A/AA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091325 | AGCAAGACTCCGTCT[-/A/AA]CAAAAAAAAAAAAAA | 57690 |
rs765369577 | snp | C/G | 1.66214e-05 | 0.00288278 | missense | TNRC6C | GRCh38.p7 | 17:78067814 | AAATGAACCTCAGTA[C/G]CAGCCAGTGGGAGGA | 57690 |
rs765411967 | snp | C/T | 0.000100944 | 0.00710364 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097867 | AGTGTTGCAGGTACG[C/T]GCCTGGCCTCTAGAC | 57690 |
rs765414947 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071248 | CTCCATGTTTGTTAT[A/G]TGTGTCAGAAGACAC | 57690 |
rs765455005 | snp | C/G | 1.66438e-05 | 0.00288472 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083178 | GCTGGTGAGTGGATA[C/G]ACCCATGCAAGTTAG | 57690 |
rs765481882 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072654 | TTGGGAGCCCAAGGC[A/G]GGAGAACCACTTGAG | 57690 |
rs765505580 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006507 | TTCTTCTTCTTCTTC[-/T]TTCTTCTTCTTCTTC | 57690 |
rs765522253 | snp | A/C | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108245 | CCGCACCCCCGCCAC[A/C]GGCTGGCCCCCCCCC | 57690 |
rs765529554 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079874 | TGTCCCAGTCTTTGT[C/T]GAGAAAATTATTCAG | 57690 |
rs765561196 | snp | A/G | 0.000126111 | 0.00793976 | missense | TNRC6C | GRCh38.p7 | 17:78104616 | CGTCCAGCCAGCCGC[A/G]GCTCAGCGCAGCGGG | 57690 |
rs765580661 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023154 | AAAATTAACAACATA[A/T]CGTATGCGGGAGGAT | 57690 |
rs765585411 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026821 | GCTAAGAGATGAGGG[C/T]GCCCAGGTTCCAATG | 57690 |
rs765593640 | in-del | -/AG | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010432 | AGTTTAATATCAATC[-/AG]AATGAAAAGTAGTAA | 57690 |
rs765595535 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78051325 | CCGGTCATCCAGAGC[A/G]GTACCACGACCAATA | 57690 |
rs765610091 | snp | A/G/T | 3.33618e-05 | 0.00408412 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087106 | TCGGTGAGTGTCCCA[A/G/T]GGTCTTCAACAGCCA | 57690 |
rs765620774 | snp | A/G | 1.65696e-05 | 0.00287828 | missense | TNRC6C | GRCh38.p7 | 17:78049532 | GAAACTTGCTGCCAC[A/G]AGAGAGCACAGAACC | 57690 |
rs765653484 | snp | A/G | 6.9389e-05 | 0.0058898 | intron-variant | TNRC6C | GRCh38.p7 | 17:78104470 | CTGTTCACGTGCCCC[A/G]TCTTGCTGTTGCAGG | 57690 |
rs765653839 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067002 | ACAGAGAAGATTCGC[A/G]TGGTTCCTATGCAAG | 57690 |
rs765672886 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007368 | TGATGAATATTAGCA[A/G]CATCAAGGTTTACGT | 57690 |
rs765678612 | snp | A/G | 0.000163975 | 0.0090532 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077416 | GACATAAACTTACTT[A/G]TTTATAGTTAATACC | 57690 |
rs765753060 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044062 | ATCTCCTTTCTTTTG[C/G]GTATATACCTAGGAT | 57690 |
rs765759682 | snp | A/G | | | utr-variant-5-prime, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78048990 | TTCCATCACAGGAAC[A/G]GAGACTGAATCTGCC | 57690 |
rs765797389 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005218 | TTTTTATTATTCATT[A/G]TGAAATTCCTCATTT | 57690 |
rs765800330 | in-del | -/AAC | | | cds-indel, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107329 | GTAACTCTGAGATTA[-/AAC]AACAAGTTCGTGGCT | 57690 |
rs765820183 | snp | A/G | 1.65644e-05 | 0.00287783 | missense | TNRC6C | GRCh38.p7 | 17:78075234 | GGCTGCCGCCCGCCA[A/G]TCTCCAAAGAGTCTT | 57690 |
rs765852133 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018222 | ACCTCCACCTCCCGG[A/G]CTCAAGTGATTCTTC | 57690 |
rs765865788 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039311 | AATTTCAAATCTTGC[-/C]CCCCCCCCCCACTCC | 57690 |
rs765873516 | snp | A/G | 1.6643e-05 | 0.00288465 | missense | TNRC6C | GRCh38.p7 | 17:78103433 | ATGGTTCTACACTGC[A/G]GACATTGTGTTTGCA | 57690 |
rs765899893 | snp | A/G | 1.65666e-05 | 0.00287802 | missense | TNRC6C | GRCh38.p7 | 17:78087000 | AAATCGGCCATGGAC[A/G]GCTTCCCCTCGCACC | 57690 |
rs765969957 | snp | C/G | 1.96489e-05 | 0.00313433 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092883 | TATCTTCTGGTGTCT[C/G]TCAACTGGAGAGTAT | 57690 |
rs765974589 | snp | C/T | 1.96941e-05 | 0.00313794 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075130 | CTTCTGTTTGTTGTG[C/T]TCCAGGCGCTCTGCT | 57690 |
rs765979691 | in-del | -/AG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030353 | GTGTGTAGTAGAGAC[-/AG]GGTTTCACCATTTTG | 57690 |
rs766053855 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042744 | TGATGGTAGTGGTCA[G/T]CATGATGCTGGTGGT | 57690 |
rs766057932 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023885 | AAGGCCAGGGTGGGT[C/G]GATCACCTATGGTCA | 57690 |
rs766085765 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083685 | CTAGAAGCACAGGAG[A/G]AAAATTGCTTTATTA | 57690 |
rs766122340 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055925 | ACCATGACCTGCTGA[C/T]ATTTCTAAAATATTA | 57690 |
rs766133538 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051912 | CAAGTGTCCAGTGAG[A/G]ACAATAAAAGGTCCC | 57690 |
rs766168812 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033015 | AGTTTACAATCAAAC[A/G]TGCTACTTTCCCAAT | 57690 |
rs766180461 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068722 | TTGCTTAAACCTGGG[A/T]GGCGGAGGTTGCAGT | 57690 |
rs766180867 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055001 | ACACCACTGCGGACT[A/G]CTGTACACCACTGCA | 57690 |
rs766230497 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008017 | GACATGCTCATCTAT[A/G]ATACTCCTCTACCTT | 57690 |
rs766230681 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020448 | AAAAGCTTGTGATCT[C/G]TCACAACTTGTAGTT | 57690 |
rs766250362 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094564 | ATGCCTCAGCCTCCC[A/G]ATTAGCTGGGACTAC | 57690 |
rs766274709 | snp | A/G | 3.34963e-05 | 0.00409232 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086511 | TCAACAGGCATACCA[A/G]CGTTTACAAATCCAG | 57690 |
rs766283899 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019243 | TAGCAAGGGTAGACT[A/G]GAGGCTAACGAGGCT | 57690 |
rs766320308 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032706 | AATTTAAAAGAAACA[A/T]GGCACAAGTCATATT | 57690 |
rs766334010 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045412 | TTGCTTCCTGCCAGT[A/G]TTGCCCCATTGGTGG | 57690 |
rs766382265 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070117 | AAAATCAGAGCTCTC[C/T]GCTCATGAGGAGTAG | 57690 |
rs766382988 | snp | A/C | 1.6604e-05 | 0.00288127 | missense | TNRC6C | GRCh38.p7 | 17:78093017 | ACGATTTAATCCAGA[A/C]CAGTGAGTCACCAGC | 57690 |
rs766406447 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057950 | GTATTTTAGGAAATG[C/G]AGTATAGCTTCCTAA | 57690 |
rs766415159 | snp | G/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106104 | ATAGATACTTGTAAA[G/T]AATGGATGGTTCCGT | 57690 |
rs766448727 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100060 | GGGTCATGCTTAGGC[A/G]AGAGGTTGGTTACCA | 57690 |
rs766457012 | snp | A/G | 3.46867e-05 | 0.00416439 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077242 | CCTTCCCCAAGCCTG[A/G]AGCTCCCCCTTTCAC | 57690 |
rs766488075 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103726 | TGAAGGTGTGGGCAG[C/G]GCTGGTTTCTCCTGA | 57690 |
rs766491515 | in-del | -/CAC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038748 | ACAGCATTGATAGAT[-/CAC]CACTTTTCACTTACC | 57690 |
rs766505057 | snp | A/G | 8.32369e-05 | 0.0064507 | missense | TNRC6C | GRCh38.p7 | 17:78098505 | CCACCTGGGGTGCCA[A/G]CCCCCTCGGCTGGAC | 57690 |
rs766523537 | snp | C/T | 1.66718e-05 | 0.00288715 | missense | TNRC6C | GRCh38.p7 | 17:78098402 | TCCCACACGCAAGCC[C/T]CTCTGTCTCATGAAC | 57690 |
rs766542875 | snp | C/T | 1.67114e-05 | 0.00289057 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087110 | TGAGTGTCCCATGGT[C/T]TTCAACAGCCACATC | 57690 |
rs766553751 | in-del | -/AAAAGA | | | upstream-variant-2KB, cds-indel | TNRC6C | GRCh38.p7 | 17:78004214 | AACGTTTGATGGAAG[-/AAAAGA]AAAAGAAAAAGCAGG | 57690 |
rs766601206 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009436 | GTGCTTTTAGCCAGA[C/T]TTGTTTAACTTCATA | 57690 |
rs766661725 | snp | A/G | 1.71988e-05 | 0.00293243 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067933 | CAAAAGGTAAGTACA[A/G]CACTCTTAACGACGG | 57690 |
rs766682255 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039266 | GAACCAGTTGAACTT[C/T]TGCTAGGCTGCAGGT | 57690 |
rs766682346 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025294 | TAGTTTTGCCTTCTC[C/T]AAAATGTCACGTAGT | 57690 |
rs766692029 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076583 | ATTTGCTAATCTGGC[-/A]AACCCTAAATTGGGA | 57690 |
rs766720223 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005164 | TTTTTTTAAATTGAT[C/G]GTTAAAAAACGAGAA | 57690 |
rs766728281 | snp | A/G | 3.9336e-05 | 0.00443469 | missense | TNRC6C | GRCh38.p7 | 17:78104640 | CAGCGGGCAGCTCCC[A/G]TGGCCTGGTACGCAG | 57690 |
rs766731543 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038206 | AGTTTTGTACATGAA[C/T]ATGAATAAAATCTGA | 57690 |
rs766732484 | in-del | -/ACATACCAAGAA | 1.80455e-05 | 0.00300373 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050311 | GGAGGGAAGGAACGG[-/ACATACCAAGAA]GAGAAGGCCGAAGGC | 57690 |
rs766744413 | in-del | -/CTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100210 | CTAGAGGACGGTGAC[-/CTT]CTTCTCATAGCTCTA | 57690 |
rs766747080 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017205 | TATTTGGTCTTTATG[C/T]CTTTTTAAAAATGTC | 57690 |
rs766823087 | snp | A/G | 1.89759e-05 | 0.00308019 | missense | TNRC6C | GRCh38.p7 | 17:78104783 | GACAGCAGGGTGATA[A/G]GCAGCCCCACGCCGC | 57690 |
rs766842690 | snp | G/T | 1.8251e-05 | 0.00302079 | missense | TNRC6C | GRCh38.p7 | 17:78050194 | CCTACCGTACAGCCT[G/T]GTGGTGAACACATGA | 57690 |
rs766844925 | snp | A/C | 1.69327e-05 | 0.00290965 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064863 | GCAGCGGGTGGGGAG[A/C]TCACCCTGCAGAGCC | 57690 |
rs766849792 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003435 | CAAGAACAGGGTGTT[A/G]TGGAAAAGGAGCATT | 57690 |
rs766850326 | snp | C/T | 1.6649e-05 | 0.00288518 | missense | TNRC6C | GRCh38.p7 | 17:78049652 | CTTCACCCAACCCTA[C/T]CAATGCAATGCAGAC | 57690 |
rs766861264 | snp | C/T | 1.69977e-05 | 0.00291523 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064684 | CTTTTCTCTGATGCA[C/T]TTTCATTATTTTCTC | 57690 |
rs766861269 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082331 | TGATCACATGGGGAT[G/T]AAGTAATTCTTTAAC | 57690 |
rs766861372 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106928 | TGCAGATCCACAAAA[G/T]CTGGTTTTATAGAGG | 57690 |
rs766865216 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077762 | CCCAGAAATAAAGAT[A/G]ACATCTCTTGCAAGG | 57690 |
rs766867485 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090278 | GCACCTGTTTATTTA[A/G]ACAGGACAGACACTC | 57690 |
rs766869012 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046761 | GGCATGTATACGATA[C/T]AAGGGATCTACTTTC | 57690 |
rs766892758 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084528 | CCAGAGACACATGCT[A/G]TGTGTCCTCGCTTTA | 57690 |
rs766933409 | snp | G/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010987 | GGGGCGCCTCCCGAG[G/T]GCACTTCTCCTGAGT | 57690 |
rs766933507 | in-del | -/C | 1.69315e-05 | 0.00290955 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064984 | GCAATTTGGAAATGA[-/C]TCAAAGTATTGAATT | 57690 |
rs766951465 | in-del | -/AACTTTACC | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010248 | TGCAGTGAGGTATTA[-/AACTTTACC]ATGCGTTCAGTTTGT | 57690 |
rs766954836 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041232 | TCCAGCGTGTGAGTG[A/G]TAGCCCGGCGTCCCT | 57690 |
rs766958610 | snp | C/T | 3.1869e-05 | 0.00399167 | missense | TNRC6C | GRCh38.p7 | 17:78051311 | GGGATAGAAACAACC[C/T]GGTCATCCAGAGCAG | 57690 |
rs766995424 | snp | A/C | 0.00990475 | 0.0696726 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093027 | CCAGAACAGTGAGTC[A/C]CCAGCCAGTCCTCCC | 57690 |
rs767005911 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097498 | CTCAAAGAAGCTCAT[G/T]CTGCTTCTTGCCCTT | 57690 |
rs767021158 | snp | A/G/T | 3.35961e-05 | 0.00409843 | missense | TNRC6C | GRCh38.p7 | 17:78093113 | ATGGCTCTAGCATCA[A/G/T]CTGGCCCCCAGGTAA | 57690 |
rs767063820 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089257 | ACAGGCGTGAGCCAC[C/T]GTGCCCGACCACTTA | 57690 |
rs767075337 | snp | A/G | 0.00263806 | 0.0362225 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104602 | GCAGTCCAGCAGCGC[A/G]TCCAGCCAGCCGCGG | 57690 |
rs767176676 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022856 | AAATGGACAGTTGCA[C/T]CTGTACTGATGCAGT | 57690 |
rs767183332 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78103517 | TCCGGTACAGCTCCA[A/G]GGAGGAGGCTGCCAA | 57690 |
rs767220725 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107943 | CTAACTTTCACCAAG[C/T]ACTTTGAGCACAGTG | 57690 |
rs767233947 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035211 | GTCCCATGTTGTTAC[A/G]GTGTTGGCACAGGGA | 57690 |
rs767241960 | snp | A/G | 8.14664e-05 | 0.00638174 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051150 | GTGGATCGGGGGGCC[A/G]GTACCGGTCAAACAG | 57690 |
rs767250236 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065884 | GGGTGTTTTGCAATG[C/T]GATATTTGTAATATT | 57690 |
rs767316473 | in-del | -/ACT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056463 | ATGGCCGGCCCAGAA[-/ACT]ACTTTTTTTTTTTTT | 57690 |
rs767321833 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092022 | TTTCTGTTGGTTATT[C/T]CCCTCCATCCAAGCA | 57690 |
rs767350910 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064631 | AGGATAGATTATCTT[G/T]AAATTATTTTGAAAT | 57690 |
rs767354026 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062180 | GTCTTTTGTGTAATT[A/G]AAGGTAATATTATAG | 57690 |
rs767366566 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102400 | CCCACACTTCAGCAC[A/G]ATAAGAAGTGGGGAG | 57690 |
rs767412709 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029599 | TGACTATACACTTAG[C/G]CCACACTAAACTTAC | 57690 |
rs767412830 | snp | A/G | 3.4617e-05 | 0.00416021 | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78049061 | GCTCAGAGAACAGTA[A/G]CATGGCTACAGGGAG | 57690 |
rs767417476 | snp | A/G | 1.82377e-05 | 0.00301969 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050682 | GGTTTGGGGGGACTC[A/G]ATAAGCTCTACTGCT | 57690 |
rs767440088 | snp | A/T | 3.32701e-05 | 0.00407847 | missense | TNRC6C | GRCh38.p7 | 17:78086533 | CAAATCCAGCAGCAG[A/T]TGTTACAGGCCCAGC | 57690 |
rs767460676 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043907 | GGATCTTATTCTTTT[C/T]ATGGCTGAACAGTAT | 57690 |
rs767475553 | in-del | -/GT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069850 | TGTGTGTGTATGTGA[-/GT]GTGTGTATGCATGCA | 57690 |
rs767504746 | snp | A/G | 9.08224e-05 | 0.00673817 | missense | TNRC6C | GRCh38.p7 | 17:78050167 | GAGAGTCCTAGTGTC[A/G]CCAGCCAGAACCCTA | 57690 |
rs767576650 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013016 | TGCCCTAAGTTTGCT[A/G]TGAAAGCAAGGACAA | 57690 |
rs767580349 | snp | G/T | 1.65723e-05 | 0.00287852 | missense | TNRC6C | GRCh38.p7 | 17:78079533 | GTGCCTCAGTTTCTA[G/T]CCCCTCAGGTCAGAC | 57690 |
rs767598602 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081117 | CTCATAGATGGCAAC[C/T]TTTATGCATCCTCAT | 57690 |
rs767602089 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037228 | CAGCAGTGCCACACT[C/T]GGCTTGCACAGCTCT | 57690 |
rs767677363 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009341 | TTTCAGTATTGTTTT[C/G]TGGGTGTTTTCATGG | 57690 |
rs767735477 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019124 | GCTGTTACAGATGAC[A/G]ATATTGAAGTGACTG | 57690 |
rs767736692 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067063 | ATACAAATTTTCCTG[C/T]CACTTGTGATGGCTC | 57690 |
rs767740971 | snp | A/G | 3.80134e-05 | 0.0043595 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102425 | GGGGAGGGCCGCACT[A/G]TCCACTGGCACGGGG | 57690 |
rs767780280 | in-del | -/TCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080904 | GTGTTAATTCATCAA[-/TCT]TCTATTATTCATAAA | 57690 |
rs767820953 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056609 | GCTAGGACTACAGGT[A/G]CCCGCCACCACGCTC | 57690 |
rs767827342 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086797 | CATTTGGTCCCTAGA[C/G]AAGCCATGAGTGTCC | 57690 |
rs767832849 | in-del | -/TTG | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109112 | CCAGGTGCCCAGCCT[-/TTG]TTGTTGTTGTTGTTG | 57690 |
rs767848233 | snp | A/G | 1.68224e-05 | 0.00290016 | missense | TNRC6C | GRCh38.p7 | 17:78093626 | CTTAAACAGAATTCC[A/G]TCCGGGAGTTCCATG | 57690 |
rs767857762 | snp | C/T | 3.31873e-05 | 0.0040734 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050478 | GTCTGAAAGGAAAAA[C/T]GACAATGGGACAGAG | 57690 |
rs767891240 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026459 | CCACTAAGAAAAAAA[C/T]TGCCAGTTAAACTGA | 57690 |
rs767900105 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063410 | AGGGGAGGGCTTGGT[C/G]TTGCTGTCTCTGGGG | 57690 |
rs767924462 | snp | A/G | 1.68832e-05 | 0.00290539 | missense | TNRC6C | GRCh38.p7 | 17:78049213 | GGAAGTGCGGCCAGA[A/G]TGTGGGGTGTAGCCA | 57690 |
rs767936571 | in-del | -/A | 1.77281e-05 | 0.00297721 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067964 | TACACCCTGAAAACC[-/A]AAGGTACTTCAGACA | 57690 |
rs767938572 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016094 | AGGCTGGGCCTTCAG[A/C]AATGACTCCCCAAAG | 57690 |
rs767944811 | in-del | -/G | 4.68132e-05 | 0.00483781 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102587 | AGCATGATCCAGGGA[-/G]GGTTCCCGCTTGGCC | 57690 |
rs767945048 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089104 | TCCCAAATTGATGGG[A/G]TTACAGGCATGCATC | 57690 |
rs767950654 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013556 | AGAAAATGTTAAAAT[A/G]GAGATACACTTCCCA | 57690 |
rs767993642 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014947 | TCTAAGGCAACTTCT[C/T]GCCACAATGTTTGCT | 57690 |
rs768000230 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099619 | ACCTCCCACTGGGTT[C/T]CTTCACGAAACATGG | 57690 |
rs768000295 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087880 | AGACACAGCTCACAT[A/G]CCTGAAGACACCAGA | 57690 |
rs768017362 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107119 | TGCGTGTGAGCATGC[A/G]TGTGCGTATGTGCGT | 57690 |
rs768053318 | snp | C/T | 3.31587e-05 | 0.00407164 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093786 | TGCTGCTCTTCCTGC[C/T]TCTGCATGGACGGTC | 57690 |
rs768073940 | snp | C/T | 9.579e-05 | 0.00691996 | intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109324 | TCCCGAGAAGATCCT[C/T]TGCAGGAGTGCGGTG | 57690 |
rs768140139 | in-del | -/G | 0.00156617 | 0.0279398 | intron-variant | TNRC6C | GRCh38.p7 | 17:78051499 | AAAAAAAAAAAAAAA[-/G]CTTATTCTCATTATA | 57690 |
rs768142013 | snp | A/G | 9.06331e-05 | 0.00673115 | missense | TNRC6C | GRCh38.p7 | 17:78050296 | AATGAAGGAAGCACT[A/G]GGAGGGAAGGAACGG | 57690 |
rs768147139 | snp | C/T | 1.65677e-05 | 0.00287812 | missense | TNRC6C | GRCh38.p7 | 17:78093751 | GTCAACCGCTACCTC[C/T]TCAAGAGTGGAGGTG | 57690 |
rs768149845 | snp | C/T | 1.65968e-05 | 0.00288065 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079370 | TGCCTGCCTTGGTAA[C/T]GTGTTTAATTCTGTC | 57690 |
rs768154567 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017871 | GTGCGCACACATACA[C/T]ACAGACATACTCTAC | 57690 |
rs768161623 | snp | A/G | 3.72898e-05 | 0.00431781 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104794 | GATAGGCAGCCCCAC[A/G]CCGCTAACCACCCTG | 57690 |
rs768162799 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048536 | CAAAGTCACTTATCT[C/T]TCAAAGCTGCCTTTA | 57690 |
rs768196752 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098627 | CTCCTTTGTAAGGAC[C/T]CCTGCCTGTAACTCT | 57690 |
rs768207942 | in-del | -/TG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016692 | CTTTAGGTCATTCTC[-/TG]TGGTTCCTCCTTTAA | 57690 |
rs768223702 | snp | A/G | 3.90198e-05 | 0.00441683 | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78104872 | ATCAGCACCAGGAGA[A/G]CCGACCCCTCCCGGG | 57690 |
rs768228787 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004708 | AAACTTCATAGTCAA[A/G]CTTGAATTTTATGGC | 57690 |
rs768242898 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094019 | AAGTCTCACTCTGTC[A/G]CCCAGGATGGAGTGC | 57690 |
rs768297293 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066260 | TCGTTGTTCACATAA[C/T]TGCAGAAGCTTCATC | 57690 |
rs768297518 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085706 | TTAGCTTTCATTCCC[A/C]TGATGTTAGGGAGAT | 57690 |
rs768300599 | snp | A/G | 1.65957e-05 | 0.00288055 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064834 | AGCAGCATGGGGGAA[A/G]CCACCCAGCAGTGGC | 57690 |
rs768315351 | snp | C/T | 1.66651e-05 | 0.00288657 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079586 | AACAGGATATAGATG[C/T]CAGTGTTTCGTGGGG | 57690 |
rs768322671 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007309 | CCAAACAAAAAATGC[-/T]TTTTGAATTATAAAT | 57690 |
rs768379284 | snp | C/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012837 | GATTTATCTATCTCA[C/T]ACTTTCTACCTGAAA | 57690 |
rs768444645 | snp | C/T | 1.66335e-05 | 0.00288383 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049392 | CCCAGCTGCCTGGCC[C/T]GTACTTGGACATGAA | 57690 |
rs768446820 | snp | A/G | 1.68326e-05 | 0.00290104 | missense | TNRC6C | GRCh38.p7 | 17:78049265 | CTCACTGCTCTGTCA[A/G]TGGTGGGGATGGAAA | 57690 |
rs768460581 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098021 | CCTTGCCCAGGCACA[A/G]TGGGCACGCTGGGCA | 57690 |
rs768489371 | snp | C/T | 3.31549e-05 | 0.0040714 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78075218 | GGCCGCCAAGCCCCT[C/T]GGCTGCCGCCCGCCA | 57690 |
rs768517494 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081721 | ACATCCCACTGCCCA[C/G]ACCTAGGCCACAGCT | 57690 |
rs768528931 | snp | C/T | 1.66117e-05 | 0.00288194 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050406 | TCTGTCTAATACTGG[C/T]TGGGGACAGACTCCT | 57690 |
rs768538053 | in-del | -/TTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088974 | TTTTTTTTTTTTTTT[-/TTT]TTTTTTTTTTTGAGA | 57690 |
rs768575206 | snp | A/C | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105822 | ACTGAGTGTCCTCGC[A/C]CTTCCTTTAGCTAAT | 57690 |
rs768577790 | snp | C/T | 2.05198e-05 | 0.00320304 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104674 | CGCTGGCCACTGGAA[C/T]GCCCCGTGCCTGGGT | 57690 |
rs768612905 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024694 | TTAAGTTTACAAAAC[A/T]ATCGAGCTGAAAGTA | 57690 |
rs768636169 | snp | G/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109160 | CATCACGGCAGAACG[G/T]TAAAGGCAGAAAGCA | 57690 |
rs768647250 | snp | A/G | 0.000199197 | 0.00997791 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051210 | AGAACCCTCTCCACC[A/G]TCCATTCGCCGCAAA | 57690 |
rs768661082 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066665 | GGGTAATTTTGATAC[C/T]GAAAATCACTTTGTA | 57690 |
rs768670037 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023769 | TGTGATCATGCCACT[A/G]CACTTCAGCTTGGGC | 57690 |
rs768696389 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098885 | ACAGCGCTTTAGGCT[C/G]TCTGCCCCCATGACT | 57690 |
rs768765429 | snp | G/T | 3.31978e-05 | 0.00407404 | missense | TNRC6C | GRCh38.p7 | 17:78093062 | CTGTTCCCCATAGCT[G/T]GTCACGTGCCAAATC | 57690 |
rs768794042 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103230 | AAGCATCCAAGTTTT[A/T]AGTTACACGTTTGGC | 57690 |
rs768806586 | snp | A/T | 9.16884e-05 | 0.00677022 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075326 | TTTTAACAAGAGGAG[A/T]TTTTCATTTCAACTG | 57690 |
rs768830349 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065228 | ATGGTGGCACATGCC[-/T]GTAATCCCAGCTATT | 57690 |
rs768851047 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018920 | GGTTTTGGCAGTCCA[C/T]GTTAGGTTAGTAAGA | 57690 |
rs768869181 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043655 | GCCTGTTATGCTAGT[A/C]ATTACTAGGTCTTAT | 57690 |
rs768942689 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082620 | AGAGCTGTGGCAAGA[C/T]AAGGGCGTTTGTAAC | 57690 |
rs768950171 | snp | A/G | 1.66167e-05 | 0.00288237 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103580 | CACAGCCACCTCAGC[A/G]CTCCAAGTAGCTCCC | 57690 |
rs768967875 | snp | A/G | 2.59454e-05 | 0.00360167 | missense | TNRC6C | GRCh38.p7 | 17:78051082 | AGCAAACCCCAAGAC[A/G]ACAATGTGAGTAACT | 57690 |
rs768995434 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074712 | GGATCTTTTGCAGAC[A/G]GAATAATCGGGAAGG | 57690 |
rs769002390 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069832 | TAGGAGGAAGAAAAC[A/G]TGTGTGTGTGTATGT | 57690 |
rs769043024 | snp | G/T | 3.34711e-05 | 0.00409078 | missense | TNRC6C | GRCh38.p7 | 17:78067895 | CCTGCAGCTCCTGGG[G/T]GAACGCCCCCAAAAA | 57690 |
rs769055678 | in-del | -/TG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030315 | CCACCACACCTGGCT[-/TG]TGTGTGTGCGTGTGT | 57690 |
rs769060018 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020007 | ATCCAGATTTTGAGA[G/T]CTTCCACTTATCCCT | 57690 |
rs769072650 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051647 | CTCTGGTGGTTTTCT[A/G]TTCAAGAAAAAAATA | 57690 |
rs769079469 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091319 | CATCAAGAGCAAGAC[C/T]CCGTCTCAAAAAAAA | 57690 |
rs769138316 | snp | A/G | 1.65765e-05 | 0.00287888 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098458 | TGCACCCACGAGGCC[A/G]CCTCCAGGGTTAACC | 57690 |
rs769140667 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095041 | GGCACCAGGGTTGTG[C/T]CAGACAGGAAAATTA | 57690 |
rs769182897 | snp | A/G | 1.79583e-05 | 0.00299647 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098368 | AGACATCAAATCGAC[A/G]TGGTCCTCTGGCCCT | 57690 |
rs769191996 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094107 | GCCTCAGCCTCCCAA[A/G]TAGCTGGAATTACAG | 57690 |
rs769195346 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010033 | ACTACAGGTGCATGC[C/T]ACAGTGCCTGGCTAA | 57690 |
rs769229709 | in-del | -/CCACCG | 5.02012e-05 | 0.0050098 | cds-indel | TNRC6C | GRCh38.p7 | 17:78086936 | CTCGTGAAGCAGCCA[-/CCACCG]CCACCGCCACCGCCC | 57690 |
rs769241629 | snp | C/T | 0.000104413 | 0.00722466 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086489 | ACTATTTTAACTCTT[C/T]GTTCTGTCAACAGGC | 57690 |
rs769248959 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009084 | CACAATTACCTGTTA[A/C]CTTAGTGAGACCCTA | 57690 |
rs769275548 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039799 | CAAGCCCGAGAGGAG[A/G]AGGGCCTGTGGGCAT | 57690 |
rs769288419 | snp | A/T | 1.68139e-05 | 0.00289943 | missense | TNRC6C | GRCh38.p7 | 17:78049274 | CTGTCAGTGGTGGGG[A/T]TGGAAAAATGGACAC | 57690 |
rs769301437 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058573 | AGTTGATCCAAGCTA[A/T]ACCAGCAGCAGTGGG | 57690 |
rs769318278 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064100 | CCAGGCTAGAGTGCA[G/T]TGGCACAATCTTGGC | 57690 |
rs769337298 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016700 | CATTCTCTGTGGTTC[C/G]TCCTTTAACATGATT | 57690 |
rs769337965 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040414 | TGTACATTTATAAAC[A/C]GAGGCTTTGATTAAT | 57690 |
rs769358349 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070733 | AAAAGTGTAATTTTT[A/G]GTAAACTTCACATAG | 57690 |
rs769369388 | snp | C/G/T | 5.03e-05 | 0.00501477 | missense, synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050541 | CTCAGGGGGGAAGAA[C/G/T]GATGGGTCCATCATG | 57690 |
rs769376567 | snp | A/T | 1.70606e-05 | 0.00292062 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067758 | TGCTCTGTTTCTAGC[A/T]TCAAAATCTATGCAA | 57690 |
rs769390307 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027097 | GGAAATAGTGGCATA[A/G]AGAAGAAGGCAGGAG | 57690 |
rs769392480 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015863 | GTTGCAGTAAGCCGA[A/G]ATCATGCCATTGCAC | 57690 |
rs769405294 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059734 | CACGCCTCTAGTCCC[A/G]GCTACTCAAGAGGCT | 57690 |
rs769429391 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040747 | TGAAAATGTTTGTGA[C/T]AATCGAAAGAATTTA | 57690 |
rs769432727 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100576 | AGCATGTGGACCCTG[A/G]GCCTGGCCCATGAAG | 57690 |
rs769458874 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011745 | GTATGTTTCATTTTT[C/T]AAGAAATTGCACACA | 57690 |
rs769459177 | snp | C/G | 1.65916e-05 | 0.00288019 | missense | TNRC6C | GRCh38.p7 | 17:78050459 | AATTTGAAGAATCCC[C/G]TAGGTCTGAAAGGAA | 57690 |
rs769489596 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107591 | TACGTACCTCTCTCA[C/G]GAGTGAACTCAGATT | 57690 |
rs769513981 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022500 | CAGTCATTTAAGAAA[A/G]ATTAACAGCAGCATG | 57690 |
rs769525092 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066570 | GTTTATCAGCCTTGT[A/T]TCTTCATTGAAGACC | 57690 |
rs769525895 | snp | A/G | 1.65935e-05 | 0.00288036 | missense | TNRC6C | GRCh38.p7 | 17:78083116 | CTATTAACCTCGCCA[A/G]TTAATCCTCAACATA | 57690 |
rs769564663 | snp | C/T | 7.03705e-05 | 0.0059313 | missense | TNRC6C | GRCh38.p7 | 17:78051217 | TCTCCACCGTCCATT[C/T]GCCGCAAAATGGAAA | 57690 |
rs769575639 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005780 | CTTCAGTATCTCATA[C/T]TTAAAATGAGAAAGG | 57690 |
rs769597709 | snp | A/G | 3.54654e-05 | 0.00421087 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077148 | TTTGTCTGCTGATGG[A/G]CACTGCACACAGCTC | 57690 |
rs769614689 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079275 | CTTGGGTACAAGTTG[A/G]CAGTGGTAGGAAGTA | 57690 |
rs769619214 | snp | C/G | 2.34398e-05 | 0.00342335 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064924 | TGTTGCTGCCTCAGC[C/G]CTGTGCAAACCAGGT | 57690 |
rs769637428 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099400 | TTATAAAAGAATGAG[A/T]TTTATTGGACTTACA | 57690 |
rs769662368 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096090 | CGCTGGGATTACATG[C/T]GTGAGCCAGTGCGCA | 57690 |
rs769682607 | snp | C/T | 0.00016142 | 0.00898244 | missense | TNRC6C | GRCh38.p7 | 17:78104550 | AAGTGAATCGCTTCT[C/T]AGCCCAAGGCCAGGC | 57690 |
rs769684082 | snp | A/G | 1.66299e-05 | 0.00288352 | missense | TNRC6C | GRCh38.p7 | 17:78049403 | GGCCTGTACTTGGAC[A/G]TGAAGGAACCGTGGC | 57690 |
rs769720413 | in-del | -/TCTGCATTTTCCAGTTATGACTTTACCTTTATGTTTTTAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063709 | GTACCATAGAAACTG[lengthTooLong]TCTGCCATCTTCTCA | 57690 |
rs769721714 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065466 | ATAATACAAATAAAT[A/G]CAAAAGTCAAAGCAA | 57690 |
rs769722756 | in-del | -/AATA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077426 | TACTTATTTATAGTT[-/AATA]CCTCTATTTTTAAAT | 57690 |
rs769756127 | snp | A/G | 1.7098e-05 | 0.00292381 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067927 | GGACTTCAAAAGGTA[A/G]GTACAACACTCTTAA | 57690 |
rs769760692 | snp | C/T | 3.48353e-05 | 0.0041733 | missense | TNRC6C | GRCh38.p7 | 17:78075225 | AAGCCCCTCGGCTGC[C/T]GCCCGCCAATCTCCA | 57690 |
rs769770607 | snp | C/T | 3.36746e-05 | 0.00410319 | missense | TNRC6C | GRCh38.p7 | 17:78086504 | CGTTCTGTCAACAGG[C/T]ATACCAACGTTTACA | 57690 |
rs769773145 | snp | C/G | 1.65905e-05 | 0.0028801 | missense | TNRC6C | GRCh38.p7 | 17:78087082 | CCAACACCTTTGCTC[C/G]TTACCCTCTCGGTGA | 57690 |
rs769804408 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034740 | TTTGAAGCCCTGGGC[A/G]GGTGAATTGCTTGAG | 57690 |
rs769820985 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078373 | CTCATTACACAGAGT[A/G]AAAACTACAGCTACA | 57690 |
rs769829848 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043466 | CATAGAAGGTATATA[A/T]ATTTATGGGTTACAT | 57690 |
rs769872773 | snp | C/T | 3.48766e-05 | 0.00417577 | missense | TNRC6C | GRCh38.p7 | 17:78050110 | AAGCCCCCAAACCAG[C/T]ATTCCAACAGTGACA | 57690 |
rs769906951 | snp | C/T | 3.42883e-05 | 0.0041404 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086810 | GACAAGCCATGAGTG[C/T]CCCTTCCCACCTAGT | 57690 |
rs769907469 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009475 | GTTTTCATACAAAAA[C/G]CTCAAAGTTAATCTT | 57690 |
rs769977856 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017831 | CACTGTCTAGGCTGG[-/T]TGGGAGTGAGTTTGT | 57690 |
rs769978651 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029225 | ACTAAAATTCAGTAG[C/T]ACGATCATACCTTGC | 57690 |
rs769983109 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055256 | TGATAACTAAGACAC[A/G]AACGCACACGTTAGC | 57690 |
rs769988543 | snp | C/T | | | intron-variant, downstream-variant-500B | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012710 | TATGAGAAGTCAGGC[C/T]CTAAGGAAAGTACAA | 57690 |
rs770002518 | snp | A/C | 1.75124e-05 | 0.00295903 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093155 | ACTTCTGTGCAACAG[A/C]AGCAGGTCAGAATGT | 57690 |
rs770014203 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093862 | GAGGCAGGGATGATA[C/T]AAGGCACAGTTGGCG | 57690 |
rs770031021 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053235 | GAATTTGTGATTCCA[A/G]TTGTTTACTAATATA | 57690 |
rs770035315 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023014 | AGGAGAGCTGGGCAT[A/G]GTGGTATGCACCTAT | 57690 |
rs770036392 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054811 | ACACTACTATACACC[A/G]CTGCAGACTACTGTA | 57690 |
rs770051680 | snp | A/G | 5.03208e-05 | 0.00501576 | missense | TNRC6C | GRCh38.p7 | 17:78091469 | AACATGAATGTCAAC[A/G]GCATGGACATGACCG | 57690 |
rs770081832 | snp | G/T | 1.65902e-05 | 0.00288008 | missense | TNRC6C | GRCh38.p7 | 17:78049636 | ACTAACCCCATGAAC[G/T]CTTCACCCAACCCTA | 57690 |
rs770085798 | snp | A/G | 3.32984e-05 | 0.00408021 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050898 | ACACTTGGGGGATGG[A/G]AAAAAAAATGGATCT | 57690 |
rs770094890 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097072 | AGGGAATCATGAGCC[A/G]GGTGTGGTGGCATGC | 57690 |
rs770095357 | snp | A/C | 1.66087e-05 | 0.00288168 | missense | TNRC6C | GRCh38.p7 | 17:78093074 | GCTGGTCACGTGCCA[A/C]ATCTGACAGTGATAA | 57690 |
rs770126126 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085308 | TTCTAATTTTAAAAC[A/G]ATGTATTCTGTTCTT | 57690 |
rs770149188 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78104400 | GCTTCCATGTGGGGC[C/T]GTTCCCAATACAGAG | 57690 |
rs770154280 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080788 | TCTAGCATTCTAGCA[C/G]AGAGGGAAAAAACTG | 57690 |
rs770161013 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78050636 | ACACAGGTTGGGGAG[A/G]CAGCAACAACAAAGC | 57690 |
rs770196974 | snp | A/C | 1.80484e-05 | 0.00300398 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091393 | AGAGCTTTAGAATGA[A/C]GTCATTTAGAGGAGC | 57690 |
rs770208576 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069546 | ATGCCACTCTGCCCA[A/G]CTAATTTTATTTTTT | 57690 |
rs770229432 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061777 | ATTTTGAAACATGAT[A/G]CTTGCAAGTCGTTTG | 57690 |
rs770251104 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050226 | CTCCTGGGCCAAAGC[A/G]GCATCTTCTGGAACT | 57690 |
rs770275187 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009006 | CCTATTCATAAACTA[A/C/G]CCCTTTGTAAATTCT | 57690 |
rs770284980 | snp | C/T | 1.65836e-05 | 0.0028795 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098479 | AGGGTTAACCAATCC[C/T]AAGCCCTCCTCCACC | 57690 |
rs770328577 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019925 | CCATAAGTGAGGATC[G/T]GAAAAGAGTTTATGG | 57690 |
rs770331662 | snp | A/G/T | 3.3578e-05 | 0.00409733 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087130 | ACAGCCACATCAGGT[A/G/T]GAGAGGGTACCTGGA | 57690 |
rs770349780 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098446 | CAGAAACAGTACTGC[A/G]CCCACGAGGCCACCT | 57690 |
rs770381381 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018659 | CCATGTATCTTACTT[A/G]CACATCAAGTTTATT | 57690 |
rs770386514 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014705 | GAGTAGAAAATACCT[C/G]TGAACGGCATTTCTC | 57690 |
rs770424028 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099267 | GAGCTATGCTTGAGC[C/T]ACTGCACTCCAGCCT | 57690 |
rs770432155 | snp | C/T | 0.00056395 | 0.0167826 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049908 | AAGTGCTAAACAAAA[C/T]GGATCCAGCAGTGCT | 57690 |
rs770458742 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015785 | GGCGTGGTGGTGGGC[A/G]CCTGTGATCCCAGCT | 57690 |
rs770470913 | snp | A/G | 3.35227e-05 | 0.00409393 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077186 | CTTTCTCCAATCAGG[A/G]TGGCGGCCTCGTGGA | 57690 |
rs770519288 | in-del | -/AA | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106566 | AAAATGAAAAAAAAG[-/AA]AAAGAGGAAAAAAAA | 57690 |
rs770538968 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086365 | AAAAAAAAAAACAGT[A/G]TGTGTCAGCCACAGT | 57690 |
rs770548234 | snp | C/T | 1.6793e-05 | 0.00289763 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050544 | AGGGGGGAAGAACGA[C/T]GGGTCCATCATGAAC | 57690 |
rs770560189 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016187 | CTAGAGCACAGTGCC[A/G]CTGCCGCAGACCAGG | 57690 |
rs770591373 | snp | G/T | 1.80693e-05 | 0.00300571 | missense | TNRC6C | GRCh38.p7 | 17:78050635 | AACACAGGTTGGGGA[G/T]ACAGCAACAACAAAG | 57690 |
rs770631051 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088526 | CATACTGAGCCATGC[C/G]TTAATTTCTTCATCT | 57690 |
rs770648399 | snp | C/T | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003981 | AATGAATGAGACAGC[C/T]GGCTACTGAAGAAGT | 57690 |
rs770658131 | snp | C/T | 3.57417e-05 | 0.00422724 | missense | TNRC6C | GRCh38.p7 | 17:78050144 | ATGGGAAAGGATCAA[C/T]AGGGTGGGAGAGTCC | 57690 |
rs770666252 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103688 | CCTCCCACTTCTGGA[-/G]GCTGGAAGTCTGATA | 57690 |
rs770677552 | snp | A/G | 1.66482e-05 | 0.0028851 | missense | TNRC6C | GRCh38.p7 | 17:78067883 | AAAGCACCTCCTCCT[A/G]CAGCTCCTGGGGGAA | 57690 |
rs770679990 | snp | C/T | 4.99014e-05 | 0.00499482 | missense | TNRC6C | GRCh38.p7 | 17:78049418 | ATGAAGGAACCGTGG[C/T]GACAGGCAACCCTTC | 57690 |
rs770695339 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033894 | CACAGCCAGATGCAT[C/T]TTTCTAACTCACCAC | 57690 |
rs770700334 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069743 | TATTGATATGAAAAG[A/T]TCACTAAAGTACATT | 57690 |
rs770703781 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016626 | CTCCATTCCTGAGTA[C/T]AGCTGTCATTACCTC | 57690 |
rs770715681 | in-del | -/AGT | 1.68556e-05 | 0.00290302 | cds-indel | TNRC6C | GRCh38.p7 | 17:78049264 | GCTCACTGCTCTGTC[-/AGT]GGTGGGGATGGAAAA | 57690 |
rs770738026 | snp | A/G | 0.000224215 | 0.0105857 | missense | TNRC6C | GRCh38.p7 | 17:78104598 | GCTGGCAGTCCAGCA[A/G]CGCGTCCAGCCAGCC | 57690 |
rs770743940 | snp | A/G | 0.000121426 | 0.00779089 | missense | TNRC6C | GRCh38.p7 | 17:78051424 | GCCGGTACTCAGCTG[A/G]ATCGATCACCGTTGC | 57690 |
rs770748293 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78046081 | TTGATTATTGTTTCA[C/T]ATGTTAATGGCTTAT | 57690 |
rs770775719 | snp | C/T | 4.07456e-05 | 0.00451344 | missense | TNRC6C | GRCh38.p7 | 17:78104679 | GCCACTGGAACGCCC[C/T]GTGCCTGGGTGGCAA | 57690 |
rs770823021 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106146 | AAACAAGCACTTGGG[C/T]GTGGGTTGTGACTGC | 57690 |
rs770837940 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076800 | GTAGGTCAAAAACAA[A/G]TGTCATGGAATTCAA | 57690 |
rs770848567 | snp | C/T | 1.78185e-05 | 0.00298478 | missense | TNRC6C | GRCh38.p7 | 17:78050773 | GACAAGTCACCCACC[C/T]GGGGTGAGCCTCCAA | 57690 |
rs770873005 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083909 | TATATACACTAAAAG[A/T]CCCAGTTAATTATTT | 57690 |
rs770886873 | in-del | -/A | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106055 | TATAAAGTTAAAGAG[-/A]AAAAAAAAAAAAAAC | 57690 |
rs770905421 | snp | A/G | 7.34997e-05 | 0.00606172 | missense | TNRC6C | GRCh38.p7 | 17:78051230 | TTCGCCGCAAAATGG[A/G]AATTGATGATGGTAC | 57690 |
rs770930955 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051481 | TGTTTCTTTACAAGT[-/A]AAAAAAAAAAAAAAA | 57690 |
rs771027610 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058498 | CAGGGATTTCATCTC[C/T]GAACTCAGATTTCAC | 57690 |
rs771040587 | snp | A/G | 1.70188e-05 | 0.00291704 | missense | TNRC6C | GRCh38.p7 | 17:78049168 | CCTTCTAATCAGAGT[A/G]CCCTTGGAGCAGGGG | 57690 |
rs771046268 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011640 | AGTAAAGCTTCTTTT[A/G]ACATTTATGTACAAG | 57690 |
rs771068239 | snp | A/G | 1.77464e-05 | 0.00297874 | missense | TNRC6C | GRCh38.p7 | 17:78073070 | GCCTTGAAGAGTAAC[A/G]ATATGAATCTTGATC | 57690 |
rs771085260 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082723 | TCCCAGAGCTATGAA[C/T]ATCTGCTTTTCTGGG | 57690 |
rs771098767 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094573 | CCTCCCGATTAGCTG[C/G]GACTACAGGCGTGCA | 57690 |
rs771101393 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022400 | TGATAACATTCATCT[A/G]TGATTTGCTTACTTC | 57690 |
rs771115020 | in-del | -/AAGAAAAATACGCTATA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029452 | ACATAGGAAAGGGAC[-/AAGAAAAATACGCTATA]AAGAATTTTTAAAAG | 57690 |
rs771146075 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095853 | ATTTGAAACCAGCCT[A/G]GGCAATATAATGAGA | 57690 |
rs771155300 | snp | A/C | 1.70217e-05 | 0.00291729 | missense | TNRC6C | GRCh38.p7 | 17:78049827 | ACTGTCCCCAGGTAA[A/C]CCTGCCACAGGAAAT | 57690 |
rs771166276 | snp | A/C/G | 3.32531e-05 | 0.00407746 | missense | TNRC6C | GRCh38.p7 | 17:78086916 | CGCCAGCTGGCCCAG[A/C/G]CCCTGCTCGTGAAGC | 57690 |
rs771186103 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018563 | TGGAGCAAATGGTAG[C/G]CAGATTGCATGGGAA | 57690 |
rs771188000 | snp | A/G | 8.55278e-05 | 0.00653885 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083019 | TAACAGAGATACAAC[A/G]GCTAATAGTATATTT | 57690 |
rs771194607 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034521 | CCCGTGAGGCTTCCC[C/G]AAGCAGCTCTGTCTC | 57690 |
rs771204503 | snp | C/G | 2.25228e-05 | 0.00335572 | missense | TNRC6C | GRCh38.p7 | 17:78091578 | TGCCCAGTGCCGCTT[C/G]CCCCCTGGAGCAGAA | 57690 |
rs771204827 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065307 | CCCTGAGCCATGACT[A/G]TACCACTCATGAGCC | 57690 |
rs771288815 | in-del | -/TTCTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006550 | TTCTTCTTCTTCTTC[-/TTCTT]CTTCTTCCTTCTTCC | 57690 |
rs771313148 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006328 | ATACTCTCAGAAGCA[C/T]TGTGAATTTACATAA | 57690 |
rs771333572 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | TNRC6C | GRCh38.p7 | 17:78079489 | CAGTGCAGCCTCTTA[A/G]CTCTTCCCAGCCCAG | 57690 |
rs771340018 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107370 | TTTCCTCATAGAATG[C/T]GACTGTTGAAGAACA | 57690 |
rs771342312 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095258 | GTGCCATGGTGTGAA[C/G]AAGATGGCCCGAGAA | 57690 |
rs771381717 | snp | C/T | 3.11969e-05 | 0.00394936 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78102523 | CAGCAGCTGGCTCGT[C/T]CTTCGAAACCTCACT | 57690 |
rs771422807 | snp | C/T | 3.31197e-05 | 0.00406925 | missense | TNRC6C | GRCh38.p7 | 17:78079462 | GGACCATGCAGCAGC[C/T]GCCACAGCCACCAGT | 57690 |
rs771440030 | snp | A/C | 1.75662e-05 | 0.00296358 | missense | TNRC6C | GRCh38.p7 | 17:78049729 | ATCCCGCCCCACCTG[A/C]AAGGCCTTCCTGGTG | 57690 |
rs771458956 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030194 | TCGCTCTGTCACCCA[G/T]CCTGGAGTGCAGTGG | 57690 |
rs771462137 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073681 | TAGGAGACATACAGG[A/G]TTGGGTTCCTATGAG | 57690 |
rs771513867 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029137 | TATTCGCACAGTAGG[A/C]CCAACTGCATTCTTT | 57690 |
rs771517417 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085100 | ACTCATAGAAAAAGC[A/C]TGCAGGTTTAGAGCT | 57690 |
rs771527790 | snp | C/G | 1.66056e-05 | 0.00288141 | missense | TNRC6C | GRCh38.p7 | 17:78050909 | ATGGGAAAAAAAATG[C/G]ATCTGGATGGGATGC | 57690 |
rs771537016 | snp | A/G | 2.00946e-05 | 0.00316969 | missense | TNRC6C | GRCh38.p7 | 17:78104730 | GGGGCGGGGTGCCCC[A/G]GTACTCCAGCAGCCT | 57690 |
rs771546349 | snp | A/G | 0.000265993 | 0.0115293 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051435 | GCTGAATCGATCACC[A/G]TTGCTTGGTCCAGGT | 57690 |
rs771549670 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023872 | CCCAGCACTTTGAAA[A/G]GCCAGGGTGGGTGGA | 57690 |
rs771556093 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007320 | ATGCTTTTTGAATTA[C/T]AAATAATCTAACAGT | 57690 |
rs771571166 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027602 | GTGAGTTGAAGACCC[A/G]GGACACGCAAAGTCC | 57690 |
rs771581888 | snp | C/G | | | intron-variant, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109253 | CAGACACAGAGGCAT[C/G]ATGGCGAGCCCCGAC | 57690 |
rs771640437 | snp | C/G | 0.000117309 | 0.00765772 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077384 | TGTTTTACCTGCCTT[C/G]TAAAAAATGTGTTTG | 57690 |
rs771666347 | in-del | -/ACTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099552 | GCTCTCATGAGACTT[-/ACTC]ACTATCACGAGAACA | 57690 |
rs771690639 | snp | A/G | 1.65732e-05 | 0.00287859 | missense | TNRC6C | GRCh38.p7 | 17:78049516 | ACTTTAGGTGCTTGG[A/G]GAAACTTGCTGCCAC | 57690 |
rs771691195 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089007 | GAGTCTTGCTCTGTT[A/G]CCCAGGCTGGAGTGC | 57690 |
rs771694347 | snp | C/T | 0.000636335 | 0.0178259 | missense | TNRC6C | GRCh38.p7 | 17:78051332 | TCCAGAGCAGTACCA[C/T]GACCAATACCACCAC | 57690 |
rs771713419 | snp | C/G | | | intron-variant, nc-transcript-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78012289 | CTGTTAGATGGCAGA[C/G]ATCAGTTCCCTGTTC | 57690 |
rs771723841 | snp | A/G | 1.65754e-05 | 0.00287879 | missense | TNRC6C | GRCh38.p7 | 17:78049630 | AATAACACTAACCCC[A/G]TGAACTCTTCACCCA | 57690 |
rs771734801 | snp | C/T | 1.71018e-05 | 0.00292414 | missense | TNRC6C | GRCh38.p7 | 17:78091446 | TCTCTTTAGCTGGAC[C/T]GAACCCAAACATGAA | 57690 |
rs771747268 | snp | G/T | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049968 | TTGGGATTCAGGACC[G/T]CCTGCTGGTCCTGGA | 57690 |
rs771752986 | in-del | -/TGACTTTGTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035152 | CAGACACCATTCCAA[-/TGACTTTGTT]TGATTTTGTCAGTGG | 57690 |
rs771765038 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091326 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57690 |
rs771766129 | snp | G/T | 1.81473e-05 | 0.0030122 | missense | TNRC6C | GRCh38.p7 | 17:78050734 | AAGAGTGGCCATGCT[G/T]GGAGTGGGGCCGCAA | 57690 |
rs771768328 | snp | A/C | 1.68992e-05 | 0.00290677 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086845 | GCACCTATGTCTCTG[A/C]CTGCCAGGTTGCGCG | 57690 |
rs771806946 | snp | A/G | 1.69252e-05 | 0.00290901 | missense | TNRC6C | GRCh38.p7 | 17:78049183 | GCCCTTGGAGCAGGG[A/G]GAGCGAACAGTAATG | 57690 |
rs771823518 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044682 | ATTTTTGGAAATAAA[A/G]TTTTGTTGGCACACA | 57690 |
rs771840384 | snp | A/G | 1.68969e-05 | 0.00290657 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050367 | GCACATCCAGTTGCC[A/G]AGGAATGATCTTGAC | 57690 |
rs771854238 | snp | A/G | 1.74543e-05 | 0.00295412 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093571 | AAATTTCGTGAATCA[A/G]TGTGCCGGTGTTCTG | 57690 |
rs771864010 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099129 | CCAGCGTGGGCAACA[A/C]AGTGAGACCCCATCT | 57690 |
rs771870649 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056752 | TTACAGGCGTGAGCC[A/G]CCACGCCTGGCCCAG | 57690 |
rs771871575 | in-del | -/GGGGCC | 3.39818e-05 | 0.00412186 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050045 | TCCATTCAGGAGCTT[-/GGGGCC]ACCCCAGCCGAAGCA | 57690 |
rs771888246 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079652 | GAGCGGAGTTAATCC[A/G]TGTTTAAGAGAAGGC | 57690 |
rs771896240 | snp | A/G | 1.6867e-05 | 0.002904 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087137 | CATCAGGTAGAGAGG[A/G]TACCTGGAGTCCGTA | 57690 |
rs771905752 | snp | C/G | 1.65652e-05 | 0.0028779 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093738 | CACCATCCAGGATGT[C/G]AACCGCTACCTCCTC | 57690 |
rs771964890 | snp | C/T | 8.28384e-05 | 0.00643524 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064789 | TTGGGGAGAACCATC[C/T]TCCCCTTCTACCCTG | 57690 |
rs771986913 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065220 | AGCCAGGCATGGTGG[C/T]ACATGCCTGTAATCC | 57690 |
rs772032338 | snp | C/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010123 | CAAGCAGTCCACCCA[C/G]TTTGGCCTCCCAAAG | 57690 |
rs772041375 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015692 | CGAGGTGGGCGGATC[A/C]CCTGAGGTCAGGAGT | 57690 |
rs772041930 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098329 | GCATATGCTCCATCT[C/G]TCTGCCTTTCTAGGT | 57690 |
rs772044643 | snp | C/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105600 | TTTCTAAGTTCATAG[C/G]CTACGTGTGTGTATG | 57690 |
rs772056492 | snp | C/T | 3.46759e-05 | 0.00416374 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102548 | CTCACTCCCCAGGTG[C/T]AATATGGTGCCCCTG | 57690 |
rs772063060 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024906 | TCAAGCAACTCTCCT[G/T]CCTCAGCCTCCCGAG | 57690 |
rs772096304 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014519 | TAGTACATTTTCTTA[C/T]AGCAGGAATATCCAA | 57690 |
rs772180997 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020798 | TAGAATCCAGTATAT[A/G]TTTTAATACTAAGTA | 57690 |
rs772184064 | snp | C/T | 1.66007e-05 | 0.00288098 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103573 | GTTTTCTCACAGCCA[C/T]CTCAGCGCTCCAAGT | 57690 |
rs772261014 | snp | A/G | 1.69893e-05 | 0.00291451 | missense | TNRC6C | GRCh38.p7 | 17:78067762 | CTGTTTCTAGCTTCA[A/G]AATCTATGCAAGAAG | 57690 |
rs772263701 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072532 | TCCTTGTCTGTGGCC[C/T]TGCTGTCTTGGCATA | 57690 |
rs772287126 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032119 | ATTGGTCCATACGAA[C/G]CCATCAAGGCAGTTA | 57690 |
rs772291027 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032104 | ACTAAAGGTCTGTAC[A/C]TTGGTCCATACGAAC | 57690 |
rs772296111 | in-del | -/CAGT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085568 | ACCAACATTTCAAAA[-/CAGT]CAAATGACCAAAGCT | 57690 |
rs772313022 | snp | A/G | 2.78106e-05 | 0.00372888 | missense | TNRC6C | GRCh38.p7 | 17:78075207 | CATAATGGAATGGCC[A/G]CCAAGCCCCTCGGCT | 57690 |
rs772346333 | snp | C/T | 1.68937e-05 | 0.0029063 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049246 | GGCTCCAGCTCTGGC[C/T]TGGCTCACTGCTCTG | 57690 |
rs772354536 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072066 | TTATCTTTCAGTTAC[C/T]GTAGATGCTTCTAAA | 57690 |
rs772420014 | in-del | -/TTTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034057 | CTCCATGGCCTACTT[-/TTTTC]TTTTCTTTTGAGACT | 57690 |
rs772473199 | snp | C/T | 8.98836e-05 | 0.00670326 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073103 | GCCATGAGTAAGTCA[C/T]ACAACATCCTTTTTA | 57690 |
rs772481747 | in-del | -/TGAA | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009853 | CCACTGCCCCTGGCC[-/TGAA]TTATGATTTTTAAGT | 57690 |
rs772489052 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039060 | ACTGACGACTGAATG[C/T]TCTGCATTTGTCCTC | 57690 |
rs772534652 | snp | C/T | 9.49352e-05 | 0.00688902 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78097845 | CAGCAGCATTGCATC[C/T]GCACCTAGTGTTGCA | 57690 |
rs772551784 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083752 | CTCTCATGAAACCCC[A/G]GTCAAGAATGGCTGA | 57690 |
rs772559390 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027445 | CTGCACACAAACACC[A/G]CAACCCTCTTCTTTT | 57690 |
rs772566002 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070962 | ATACAGCATTATTCA[A/G]TGTTAATACAAAAAG | 57690 |
rs772572738 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055454 | CAGTAGGTTTGTTTA[C/T]ACGAGCATCACCACA | 57690 |
rs772617000 | snp | C/T | 3.3561e-05 | 0.00409626 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083034 | GGCTAATAGTATATT[C/T]TATGTTAAACAGGTT | 57690 |
rs772640032 | snp | A/T | 1.6574e-05 | 0.00287867 | missense | TNRC6C | GRCh38.p7 | 17:78086986 | ACCCCTCTGCAGGCA[A/T]ATCGGCCATGGACAG | 57690 |
rs772685660 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040753 | TGTTTGTGACAATCG[A/G]AAGAATTTAAAGAGG | 57690 |
rs772704457 | snp | C/T | 3.33617e-05 | 0.00408408 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049851 | AGGAAATAGCAATTC[C/T]GGGTTCAGTCAGGGG | 57690 |
rs772705259 | in-del | -/CCGCCC | 1.72002e-05 | 0.00293254 | cds-indel | TNRC6C | GRCh38.p7 | 17:78086945 | CAGCCACCACCGCCA[-/CCGCCC]CCGCCCCCGCCGCAC | 57690 |
rs772749674 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015996 | ATAGAAACTACTCTA[A/G]CTGTTATAAGCAGAA | 57690 |
rs772782013 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78013181 | AAGCTAGCTCATAGA[A/G]TCCTTGAACACCTTC | 57690 |
rs772808840 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057148 | GAAAGTATGTTAAGT[A/T]TAGTATATTGTACAA | 57690 |
rs772828471 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096930 | GATGGCCCATTTATC[C/T]TAAGTCTCCCTTTCA | 57690 |
rs772850777 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076616 | CTGACATTTAAAATA[G/T]GGAATAATGCACAGG | 57690 |
rs772857130 | snp | A/G | 1.68007e-05 | 0.00289828 | missense | TNRC6C | GRCh38.p7 | 17:78050018 | GCAGTGGCAACAATG[A/G]CGTTGGTAATATCCA | 57690 |
rs772868124 | snp | C/T | | | intron-variant, nc-transcript-variant | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78109327 | CGAGAAGATCCTCTG[C/T]AGGAGTGCGGTGTCT | 57690 |
rs772879696 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068232 | TCTCTTAAGCCAGAC[A/G]TAGAGATTTGCCAAA | 57690 |
rs772906987 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023877 | CACTTTGAAAGGCCA[A/G]GGTGGGTGGATCACC | 57690 |
rs772913990 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100146 | GGTATTGTCTGCAGC[-/T]TTTCCAGGCACACGG | 57690 |
rs772926199 | snp | A/G | 1.65712e-05 | 0.00287843 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093769 | AAGAGTGGAGGTGAG[A/G]GTGCTGCTCTTCCTG | 57690 |
rs772929871 | snp | G/T | 0.000183385 | 0.00957387 | missense | TNRC6C | GRCh38.p7 | 17:78104563 | CTTAGCCCAAGGCCA[G/T]GCGCTGCCACCCACT | 57690 |
rs772937645 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080740 | GGAGCCCTGCCCTGA[A/G]AGAGCAGCAGCATCT | 57690 |
rs772946779 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007387 | CAAGGTTTACGTTTT[C/T]CTCAGACTCTTCATT | 57690 |
rs772949665 | snp | C/G | 1.65916e-05 | 0.00288019 | missense | TNRC6C | GRCh38.p7 | 17:78050463 | TGAAGAATCCCCTAG[C/G]TCTGAAAGGAAAAAT | 57690 |
rs772960908 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036645 | GAGACTTACATAGGC[C/T]GGGCGCGTTGGCTCA | 57690 |
rs772986064 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78032847 | TAATATTTTTAGACA[A/G]CTTTACCAAGTCTCT | 57690 |
rs773055738 | snp | A/G | 0.000144071 | 0.00848616 | missense | TNRC6C | GRCh38.p7 | 17:78051218 | CTCCACCGTCCATTC[A/G]CCGCAAAATGGAAAT | 57690 |
rs773074224 | snp | A/C | 3.50809e-05 | 0.00418799 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077155 | GCTGATGGACACTGC[A/C]CACAGCTCACCCTTT | 57690 |
rs773075906 | snp | C/T | 3.15981e-05 | 0.00397467 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051114 | GGGAGGAGCTGCTTC[C/T]GTGAAACAGACAGGA | 57690 |
rs773079830 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074786 | GCAAGTCTTGCAGAA[A/G]ACTAGGGGAGGGGGT | 57690 |
rs773132346 | snp | C/T | 1.66266e-05 | 0.00288323 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071049 | TGCATTAAAATGTAG[C/T]TCATGGACTTCCCCC | 57690 |
rs773162047 | snp | C/G | 3.8681e-05 | 0.00439761 | missense | TNRC6C | GRCh38.p7 | 17:78075226 | AGCCCCTCGGCTGCC[C/G]CCCGCCAATCTCCAA | 57690 |
rs773189766 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081876 | ACCTGTGAGTACTGA[C/T]AGGAAGGACACAGAA | 57690 |
rs773241480 | snp | A/C | 1.8179e-05 | 0.00301483 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050655 | CAACAACAAAGCGCC[A/C]AGTGGCCCGGGGGTT | 57690 |
rs773244833 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094365 | AGGCCACCTAGATAG[C/T]TCCCAAAACATTGAA | 57690 |
rs773264538 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056754 | ACAGGCGTGAGCCAC[C/G]ACGCCTGGCCCAGAA | 57690 |
rs773285193 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010274 | GCGTTCAGTTTGTAA[C/T]TGGTAAACAAAACCT | 57690 |
rs773302598 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009361 | TGTTTTCATGGATTG[A/G]GTGAGGGTTTTTTTA | 57690 |
rs773303886 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014537 | CAGGAATATCCAAGG[G/T]CCAAAACAAAGTAAC | 57690 |
rs773341309 | snp | C/T | 1.66521e-05 | 0.00288544 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083181 | GGTGAGTGGATAGAC[C/T]CATGCAAGTTAGAGC | 57690 |
rs773368311 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095103 | GCAGGTTGTACAGAT[C/T]CAAGTCATAAGGGAA | 57690 |
rs773377620 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039096 | AGTGGCATGAATTAA[C/T]AACAGGCAAGTTGGA | 57690 |
rs773379560 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053788 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 57690 |
rs773384140 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016970 | CCCAGCAAAGAAGTG[G/T]CAGAGCTGAAGTTTC | 57690 |
rs773396767 | snp | A/G | 1.71085e-05 | 0.00292471 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067928 | GACTTCAAAAGGTAA[A/G]TACAACACTCTTAAC | 57690 |
rs773419956 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020913 | TACACTTGTCTGAGA[A/T]TTCCAGTCAATTGCA | 57690 |
rs773424370 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023063 | GGCTGAGGTGGGAGG[A/T]ACACTTAAGCTCAGG | 57690 |
rs773432561 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052664 | CAACAGGAGAATGTC[C/T]TGCCTGCTGCATTAA | 57690 |
rs773441814 | snp | A/G | 1.77448e-05 | 0.00297861 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050136 | TGACATCAATGGGAA[A/G]GGATCAACAGGGTGG | 57690 |
rs773472995 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020230 | AGACTACCAGCCATA[C/G]CATTAGCATTGCAAG | 57690 |
rs773506472 | snp | C/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105912 | ACTCAAGGACTCTGT[C/G]ACTGCGTTTAAAAAG | 57690 |
rs773543557 | snp | C/T | 1.78886e-05 | 0.00299065 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050769 | GGAGGACAAGTCACC[C/T]ACCTGGGGTGAGCCT | 57690 |
rs773582372 | snp | A/G | 3.59602e-05 | 0.00424014 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091404 | ATGAAGTCATTTAGA[A/G]GAGCAGGCGAATCCT | 57690 |
rs773597833 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058762 | GTATCTCAGCCATAG[C/T]AGGGATTCCAGCTGT | 57690 |
rs773598908 | snp | C/T | 3.31774e-05 | 0.00407279 | missense | TNRC6C | GRCh38.p7 | 17:78098487 | CCAATCCCAAGCCCT[C/T]CTCCACCTGGGGTGC | 57690 |
rs773609610 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102024 | GGGACACAGCCAAAC[C/T]GTATCAGATAGTTGG | 57690 |
rs773650138 | in-del | -/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010019 | TCCCAAGTAGCTGAC[-/T]TACAGGTGCATGCCA | 57690 |
rs773710688 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090204 | TGGCTTCTGGCTTCT[C/T]TTAAAAATGGCTATA | 57690 |
rs773713453 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066722 | TCTGAAGTGGAAACT[C/T]GATAGTCACTTTGTA | 57690 |
rs773739169 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78104059 | GTGTCTACTCCCTCC[A/C]TGTGACACATTCCTA | 57690 |
rs773746939 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066704 | TAGGAGGAAAAAACA[A/G]TATCTGAAGTGGAAA | 57690 |
rs773755876 | snp | A/T | 0.00017751 | 0.0094193 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077427 | ACTTATTTATAGTTA[A/T]TACCTCTATTTTTAA | 57690 |
rs773767622 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78070978 | TGTTAATACAAAAAG[A/T]TCCTGTGACTTTTAA | 57690 |
rs773805576 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094354 | TATCACTAATAAGGC[C/T]ACCTAGATAGTTCCC | 57690 |
rs773813876 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026494 | TTCATTGTCAGTTAT[A/G]ATATGCATCCCAGTT | 57690 |
rs773825405 | in-del | -/ATGGTGGTGGTGCTG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042764 | ATGCTGGTGGTGATC[-/ATGGTGGTGGTGCTG]ATGGTGGTGGTGGTG | 57690 |
rs773838219 | snp | A/G | 3.61853e-05 | 0.00425339 | missense | TNRC6C | GRCh38.p7 | 17:78050638 | ACAGGTTGGGGAGAC[A/G]GCAACAACAAAGCGC | 57690 |
rs773887817 | snp | C/G | 1.71135e-05 | 0.00292514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077355 | GCTGTTTGGAGAGAG[C/G]AAAACATGGCCTTTG | 57690 |
rs773898274 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107695 | AGAGGCACAGCCAAG[C/T]TTTCCAGCTCTCCAC | 57690 |
rs773949350 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018540 | GATATTGACATGTTT[-/G]GGGGGGGTGGAGCAA | 57690 |
rs773961906 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006212 | AAGACTTGAGGGAGT[C/G]CAGGTCTCTGAACCT | 57690 |
rs773962315 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022803 | GGCTTCTGCATCCAT[A/G]GATTTAACTAACTGT | 57690 |
rs773972114 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008898 | TAAATATATATTTAT[-/A]ATGGACTCTCCACTG | 57690 |
rs773989370 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006726 | ACAAATTGCTTATTA[C/G]TGAACAGTGATTGTG | 57690 |
rs773991102 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087292 | AAAATTTTTTAATTA[A/T]TTTTTTGAGAGATGG | 57690 |
rs774000493 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062857 | CTTAACTACTTGACC[A/G]GAAGCCTTATTGATA | 57690 |
rs774004130 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004752 | AGTTATGCCATTTGT[C/T]TTTGTTCTTACCTAG | 57690 |
rs774056584 | snp | A/T | 1.65373e-05 | 0.00287548 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093166 | ACAGCAGCAGGTCAG[A/T]ATGTGCTCCAAGCCT | 57690 |
rs774071415 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101255 | AATGCCGCCAGTCTC[C/T]TTGCTAAAACAACAA | 57690 |
rs774076794 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017989 | GTCCCACTGTTCCTT[C/T]TATCATGCTTACAAC | 57690 |
rs774092581 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078733 | ACTTTGGGAGGCTGA[C/G]GTGAGTGGATCCCCT | 57690 |
rs774107038 | snp | A/G | 8.31594e-05 | 0.0064477 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049419 | TGAAGGAACCGTGGC[A/G]ACAGGCAACCCTTCC | 57690 |
rs774145058 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042368 | TACTGTTTATTAGTT[A/G]CAAACCCTGGCCACT | 57690 |
rs774146426 | snp | A/G | 0.000193968 | 0.00984612 | missense | TNRC6C | GRCh38.p7 | 17:78104700 | TGGGTGGCAAGGGGA[A/G]CAGTGAGCTGCTGTG | 57690 |
rs774199310 | in-del | -/ATAT | 0.000421333 | 0.0145082 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78050027 | ACAATGGCGTTGGTA[-/ATAT]CCATTCAGGAGCTTG | 57690 |
rs774226728 | snp | C/T | 1.68238e-05 | 0.00290028 | missense | TNRC6C | GRCh38.p7 | 17:78050021 | GTGGCAACAATGGCG[C/T]TGGTAATATCCATTC | 57690 |
rs774227484 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085765 | TGAATGATTTGGGAC[A/G]GTTACTACCAGTGTT | 57690 |
rs774232131 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014449 | TTTCTAAATTGATCT[C/T]CTAAATAAGCCTGTT | 57690 |
rs774256188 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009711 | AGGTGCGCACCACCA[C/T]GCCCAGCTAATTTTT | 57690 |
rs774256738 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074107 | TTCCTCTGTAAGGCG[C/G]TTTACTGCCTTCTTG | 57690 |
rs774275231 | snp | A/G | 1.66032e-05 | 0.0028812 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050910 | TGGGAAAAAAAATGG[A/G]TCTGGATGGGATGCT | 57690 |
rs774328161 | snp | A/G | 1.67256e-05 | 0.0028918 | missense | TNRC6C | GRCh38.p7 | 17:78086513 | AACAGGCATACCAAC[A/G]TTTACAAATCCAGCA | 57690 |
rs774333763 | snp | A/G | 1.66921e-05 | 0.00288891 | missense | TNRC6C | GRCh38.p7 | 17:78093101 | ATAAAATCTCAAATG[A/G]CTCTAGCATCAACTG | 57690 |
rs774354095 | snp | A/G | 0.000112657 | 0.00750439 | missense | TNRC6C | GRCh38.p7 | 17:78104600 | TGGCAGTCCAGCAGC[A/G]CGTCCAGCCAGCCGC | 57690 |
rs774427505 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020078 | TTACTGGCTTAAGTC[A/G]GAAGGTTTATCACTG | 57690 |
rs774439851 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051652 | GTGGTTTTCTATTCA[A/G]GAAAAAAATATATTA | 57690 |
rs774463438 | snp | A/G | | | missense | TNRC6C | GRCh38.p7 | 17:78092993 | CCATTGATGACTCCT[A/G]TGGCCGGTACGATTT | 57690 |
rs774470494 | snp | C/G | 3.33328e-05 | 0.00408231 | missense | TNRC6C | GRCh38.p7 | 17:78049653 | TTCACCCAACCCTAT[C/G]AATGCAATGCAGACA | 57690 |
rs774523871 | in-del | -/AAG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033801 | TAGTGAGCATAAAAT[-/AAG]AAATTCATTCTTGAC | 57690 |
rs774558240 | snp | G/T | 1.7808e-05 | 0.0029839 | missense | TNRC6C | GRCh38.p7 | 17:78050774 | ACAAGTCACCCACCT[G/T]GGGTGAGCCTCCAAA | 57690 |
rs774560447 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78057827 | CTGAATTACATTTTT[G/T]TGTGTGTGTGTGTGT | 57690 |
rs774577451 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063225 | ACTCCAGCCTGGGCA[A/G]CAGAGCAAGACTCTG | 57690 |
rs774580371 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026745 | GAGATCTGCATTTCA[G/T]AAGGATCACACTGGC | 57690 |
rs774598230 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030480 | ACCAGCATCACCACA[A/C]ACACGTGAGTAATGT | 57690 |
rs774613635 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069903 | TCTACAGAATGTTCT[A/C]AATTCTCTGGAAGGG | 57690 |
rs774634227 | snp | A/C/G | 0.00259378 | 0.0359202 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064866 | GCGGGTGGGGAGATC[A/C/G]CCCTGCAGAGCCGCC | 57690 |
rs774640682 | snp | A/C | 8.82418e-05 | 0.00664177 | missense | TNRC6C | GRCh38.p7 | 17:78073085 | AATATGAATCTTGAT[A/C]AGGCCATGAGTAAGT | 57690 |
rs774657335 | snp | C/G | 4.10787e-05 | 0.00453185 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071081 | TTCCCACACTTTGTT[C/G]AAGGGCATGAAGACG | 57690 |
rs774664812 | snp | C/T | 1.65611e-05 | 0.00287755 | missense | TNRC6C | GRCh38.p7 | 17:78079491 | GTGCAGCCTCTTAAC[C/T]CTTCCCAGCCCAGTC | 57690 |
rs774674655 | snp | C/G | 1.69691e-05 | 0.00291278 | missense | TNRC6C | GRCh38.p7 | 17:78049174 | AATCAGAGTGCCCTT[C/G]GAGCAGGGGGAGCGA | 57690 |
rs774683341 | snp | C/G | 1.7607e-05 | 0.00296702 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049734 | GCCCCACCTGCAAGG[C/G]CTTCCTGGTGCTAAT | 57690 |
rs774705778 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78039007 | TGTTGGGTAATATGA[C/T]GTAGTACATCCTGCA | 57690 |
rs774707331 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106940 | AAAGCTGGTTTTATA[C/G]AGGATCATGAACTAT | 57690 |
rs774733295 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082650 | CCCTATCTTATCCAT[A/G]TGAACAGGCGCCCCT | 57690 |
rs774736962 | snp | C/T | 1.70151e-05 | 0.00291672 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086833 | CACCTAGTTAACGCA[C/T]CTATGTCTCTGCCTG | 57690 |
rs774746036 | snp | A/C | 2.48902e-05 | 0.00352767 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064933 | CTCAGCCCTGTGCAA[A/C]CCAGGTAAGCCTAGC | 57690 |
rs774773672 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062159 | CTTCTCCCAATATAT[A/G]TTATTGTCTTTTGTG | 57690 |
rs774782308 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081716 | CAGTCACATCCCACT[G/T]CCCAGACCTAGGCCA | 57690 |
rs774784375 | snp | C/T | 4.53782e-05 | 0.00476309 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091579 | GCCCAGTGCCGCTTC[C/T]CCCCTGGAGCAGAAC | 57690 |
rs774823161 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025086 | ATGAGTCACCGCGCC[C/T]GGCCAATACATTATT | 57690 |
rs774832497 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078521 | TTAGTAATCACCACA[C/T]ATTATTACCCTTTAA | 57690 |
rs774844463 | snp | A/G | 1.6593e-05 | 0.00288031 | missense | TNRC6C | GRCh38.p7 | 17:78050171 | GTCCTAGTGTCACCA[A/G]CCAGAACCCTACCGT | 57690 |
rs774846346 | snp | C/T | 1.68764e-05 | 0.00290481 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083028 | TACAACGGCTAATAG[C/T]ATATTTTATGTTAAA | 57690 |
rs774870277 | snp | C/T | 1.67733e-05 | 0.00289592 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091490 | GACATGACCGGTGGC[C/T]TGTCGGTGAAGGACC | 57690 |
rs774885440 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090086 | CAAGTAGGCAGCCCT[C/G]TGGCACTGATGGGCT | 57690 |
rs774929388 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004565 | CCTGAACAACCATGT[C/G]TAATAAATGAAGAAG | 57690 |
rs774932509 | snp | A/G | 0.000295639 | 0.0121545 | missense | TNRC6C | GRCh38.p7 | 17:78051443 | GATCACCGTTGCTTG[A/G]TCCAGGTAGGAAAGG | 57690 |
rs774948289 | snp | C/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009103 | AGTGAGACCCTAGAT[C/G]CTCTTATACTGGGGG | 57690 |
rs774960614 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038014 | ACACGGAGAGTTGCA[C/G]ATCACTGAGAAAATA | 57690 |
rs774965162 | snp | A/G | 0.000132661 | 0.00814328 | missense | TNRC6C | GRCh38.p7 | 17:78049634 | ACACTAACCCCATGA[A/G]CTCTTCACCCAACCC | 57690 |
rs774968881 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072223 | GTTGACGGTGGCTTC[A/T]GCGTGTCCTGATTTA | 57690 |
rs775025630 | snp | C/T | 3.9703e-05 | 0.00445533 | missense | TNRC6C | GRCh38.p7 | 17:78104754 | GCAGCCTGTGGGGCC[C/T]GCCCAGCGCCGACGA | 57690 |
rs775046611 | snp | A/G | 4.9708e-05 | 0.00498513 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064799 | CCATCCTCCCCTTCT[A/G]CCCTGGTGGATAATG | 57690 |
rs775064906 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065883 | TGGGTGTTTTGCAAT[A/G]TGATATTTGTAATAT | 57690 |
rs775091296 | snp | A/G | 0.000131974 | 0.00812217 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077197 | CAGGATGGCGGCCTC[A/G]TGGAAGAGCCCACGC | 57690 |
rs775098816 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033994 | TTTTTCTCTCTGGCT[A/G]TGAAGGCCCTTCATA | 57690 |
rs775118669 | snp | C/T | 9.03302e-05 | 0.00671989 | intron-variant | TNRC6C | GRCh38.p7 | 17:78073108 | GAGTAAGTCATACAA[C/T]ATCCTTTTTAAAAAG | 57690 |
rs775142706 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089062 | AACCTCCACCTTCTG[G/T]ATTCAAGCAATTCTC | 57690 |
rs775143254 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097108 | TGGTCCCTGTGACTC[C/T]GGAGGCTGAGGCAAG | 57690 |
rs775173174 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003336 | GTATCTAAGGGAAGA[A/G]GCATCCAGAGAAGGA | 57690 |
rs775213091 | snp | A/G | 8.68885e-05 | 0.00659065 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077395 | CCTTCTAAAAAATGT[A/G]TTTGAGACATAAACT | 57690 |
rs775219524 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054839 | GTACGCTACCATACA[C/T]CACTGCAGACTACTG | 57690 |
rs775223495 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100906 | TCAGCCTCCCGAGTA[G/T]CTGGGACTACAGGTG | 57690 |
rs775250439 | snp | C/T | 1.68692e-05 | 0.00290419 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049251 | CAGCTCTGGCCTGGC[C/T]CACTGCTCTGTCAGT | 57690 |
rs775265614 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027171 | AAGACTGAGGGGTCA[A/G]AAGATAACAGGGCCT | 57690 |
rs775271391 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054042 | TCACCTAGGCTATAC[G/T]GTACAGCCTGTTGCT | 57690 |
rs775271488 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066588 | TTCATTGAAGACCCA[C/G]CTAACTGTGCTCTTA | 57690 |
rs775279354 | snp | C/T | 1.6916e-05 | 0.00290822 | missense | TNRC6C | GRCh38.p7 | 17:78049187 | TTGGAGCAGGGGGAG[C/T]GAACAGTAATGGAAG | 57690 |
rs775292527 | snp | C/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011796 | TACTGTTTCACAGTT[C/G]TGCATCTTCACCAAT | 57690 |
rs775315792 | snp | C/T | 9.95537e-05 | 0.00705457 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78077193 | CAATCAGGATGGCGG[C/T]CTCGTGGAAGAGCCC | 57690 |
rs775328208 | in-del | -/C | 1.70411e-05 | 0.00291895 | frameshift-variant | TNRC6C | GRCh38.p7 | 17:78050049 | TTCAGGAGCTTGGGG[-/C]CACCCCAGCCGAAGC | 57690 |
rs775333937 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021336 | GGGCACAGGAGGGGC[G/T]TGGGCCACGCATTCA | 57690 |
rs775367234 | snp | C/G | 2.64393e-05 | 0.00363579 | missense | TNRC6C | GRCh38.p7 | 17:78049073 | GTAGCATGGCTACAG[C/G]GAGTGCCCAGGGCAA | 57690 |
rs775420002 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084032 | CTCATGCCTATAATC[C/G]CAGCATTTTGGGAGG | 57690 |
rs775426095 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072506 | AGAGCATCCTGTCCT[C/G]ATGGCAGGTGTCCTT | 57690 |
rs775436874 | snp | C/T | 3.48754e-05 | 0.0041757 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093572 | AATTTCGTGAATCAA[C/T]GTGCCGGTGTTCTGA | 57690 |
rs775437621 | snp | C/T | 5.0635e-05 | 0.0050314 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086846 | CACCTATGTCTCTGC[C/T]TGCCAGGTTGCGCGC | 57690 |
rs775485544 | snp | C/G | 3.06302e-05 | 0.00391333 | missense | TNRC6C | GRCh38.p7 | 17:78071116 | GCAAGCAGGATGAGG[C/G]CTGGATCATGAGCCG | 57690 |
rs775490503 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022662 | CAGCTCAAATTCTTT[C/G]CTTCTGAGTCCTTGC | 57690 |
rs775555981 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78079282 | ACAAGTTGACAGTGG[C/T]AGGAAGTAGAAACAA | 57690 |
rs775598187 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102326 | GTTTACCAAAGATAG[C/T]ATGGGCCTCCCAGGC | 57690 |
rs775613714 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041978 | TGATTAAATCTGATA[A/C]CTAATTAAAATTTTG | 57690 |
rs775621521 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061966 | AGATGGAGGTCTAGA[A/G]ATGATAAACAAATTC | 57690 |
rs775640860 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018250 | TTCTGCCTTAGCCTC[C/T]AGAGTAGCTGGGACT | 57690 |
rs775674276 | snp | A/T | 1.69887e-05 | 0.00291446 | missense | TNRC6C | GRCh38.p7 | 17:78091512 | TGAAGGACCCATCCC[A/T]GTCCCAGTCACGCCT | 57690 |
rs775683475 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78068818 | AAAAAAGACACAAAT[A/G]TGCGGTCATCTAGAA | 57690 |
rs775700122 | snp | C/G | 1.66687e-05 | 0.00288688 | missense | TNRC6C | GRCh38.p7 | 17:78049853 | GAAATAGCAATTCTG[C/G]GTTCAGTCAGGGGAA | 57690 |
rs775746991 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073974 | AGTACTTTCTGAGCA[G/T]CCGCACATACAGGTC | 57690 |
rs775794245 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78072816 | TTTGTTTCCAAAGTG[G/T]TAAATACAAGGGCTT | 57690 |
rs775798453 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085346 | TTTCCAGAAAAATTG[A/G]AAAAATAAAGTTTCA | 57690 |
rs775804073 | snp | G/T | 1.66496e-05 | 0.00288522 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064962 | GCATCCTGCTTGCCC[G/T]GATCTGGCAATTTGG | 57690 |
rs775809865 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016663 | ATTGCTGCAGTCTCT[C/G]CCTGCCTTCCCTTCT | 57690 |
rs775810244 | snp | A/G | 4.97855e-05 | 0.00498902 | missense | TNRC6C | GRCh38.p7 | 17:78050926 | TCTGGATGGGATGCT[A/G]ACAGTAATAGGTCAG | 57690 |
rs775862250 | in-del | -/T | 1.68533e-05 | 0.00290282 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103397 | GCTCATTCATGTCCC[-/T]GTGCTTCCTCTATCA | 57690 |
rs775883392 | snp | C/T | 1.66838e-05 | 0.00288818 | missense | TNRC6C | GRCh38.p7 | 17:78092957 | CTGGAGGTCTAAGCA[C/T]TGGGCCTCCAGGTAA | 57690 |
rs775891087 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019001 | GCTCATTGCTGTTTC[C/T]GAGACTACATGTGGC | 57690 |
rs775895131 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081630 | GGTGACTCTGCCATA[A/G]CCACTTCCCAGGAAC | 57690 |
rs775901517 | snp | C/T | 1.69152e-05 | 0.00290814 | missense | TNRC6C | GRCh38.p7 | 17:78050555 | ACGATGGGTCCATCA[C/T]GAACAGTACAAATAC | 57690 |
rs775907005 | snp | A/T | 1.66023e-05 | 0.00288113 | missense | TNRC6C | GRCh38.p7 | 17:78083140 | CAACATATGACGATG[A/T]TGAACCAGCTCTATC | 57690 |
rs775908969 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092688 | AGGTTGAGCCCTGAT[C/G]ACATCACTACACTCC | 57690 |
rs775942978 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78015805 | TGATCCCAGCTACTC[A/G]GGAGGCCAAGGCAGG | 57690 |
rs775998901 | snp | G/T | 1.66048e-05 | 0.00288134 | missense | TNRC6C | GRCh38.p7 | 17:78083062 | GTTCAAGCACAGCTT[G/T]TGCAGTTTGCAGCAA | 57690 |
rs776000049 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088755 | ACAGGCATGAGCCAT[C/T]ACACCTGGCCTAATA | 57690 |
rs776038887 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106235 | AGACTTTAAAATTTT[A/T]AAAATTTAAAAAGGA | 57690 |
rs776100073 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037778 | ATTCAGATTTAAAGC[C/T]CTTCCTCCAAGTTGC | 57690 |
rs776102025 | in-del | -/TC | 1.69714e-05 | 0.00291298 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086839 | GTTAACGCACCTATG[-/TC]TCTGCCTGCCAGGTT | 57690 |
rs776106643 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007503 | GGCCTGACTGTACCT[A/G]TGATACATGTTATAG | 57690 |
rs776150607 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78103327 | CTAGTGTTTAGTGTA[G/T]CCAATTTCATACGTT | 57690 |
rs776156457 | snp | A/T | 3.31384e-05 | 0.00407039 | missense | TNRC6C | GRCh38.p7 | 17:78093757 | CGCTACCTCCTCAAG[A/T]GTGGAGGTGAGGGTG | 57690 |
rs776164413 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087762 | ATCGACCAAATCAAC[A/G]TATATATGTTGAAAT | 57690 |
rs776199941 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039287 | GGCTGCAGGTCCCCA[A/C]AGAACAGCAATTTCA | 57690 |
rs776212280 | in-del | -/C | 1.68556e-05 | 0.00290302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064697 | CACTTTCATTATTTT[-/C]TCTACCCCTTGGAAC | 57690 |
rs776236120 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78058513 | TGAACTCAGATTTCA[C/G]TGAAATGTAGATAAT | 57690 |
rs776257667 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025982 | TAGTCTAAACCTTTC[A/T]TTTCCAGATGAGAAA | 57690 |
rs776314806 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025011 | GTTAGCCAGTGTGAT[C/G]TCAAACTCCTGACAG | 57690 |
rs776343638 | snp | A/G | 3.64518e-05 | 0.00426902 | missense | TNRC6C | GRCh38.p7 | 17:78075220 | CCGCCAAGCCCCTCG[A/G]CTGCCGCCCGCCAAT | 57690 |
rs776344094 | snp | G/T | 2.29292e-05 | 0.00338586 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064922 | CCTGTTGCTGCCTCA[G/T]CCCTGTGCAAACCAG | 57690 |
rs776350565 | snp | A/G | 0.000621311 | 0.0176145 | missense | TNRC6C | GRCh38.p7 | 17:78104768 | CCGCCCAGCGCCGAC[A/G]ACAGCAGGGTGATAG | 57690 |
rs776362087 | snp | C/T | 0.000100257 | 0.00707945 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064852 | ACCCAGCAGTGGCAG[C/T]GGGTGGGGAGATCAC | 57690 |
rs776384967 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065365 | TTAAAAAGGAAAAAA[A/G]AAAAGCCAAGATTAT | 57690 |
rs776405475 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78069762 | CTAAAGTACATTGTT[A/G]AATTAAAAGCAAGGT | 57690 |
rs776421370 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78021236 | TGGACAACCTCTCCA[C/G]AGAGTCCAGGGCTGG | 57690 |
rs776430812 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066695 | TTTTAAGATAGGAGG[-/A]AAAAAACAATATCTG | 57690 |
rs776468473 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052937 | TTTTTCTGTGAATTG[A/G]CATTTTTTTAATGCA | 57690 |
rs776485008 | in-del | -/GAGTGCA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083206 | TAGAGCACGCAGGCC[-/GAGTGCA]GATGCACGGCACCTG | 57690 |
rs776490482 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076933 | CCTGAGGCAGGGCCA[A/G]TAGTTAGGAGAATAG | 57690 |
rs776518612 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78064391 | CCACCGCATCTGACC[A/G]GTTTTAAGAAGCCAA | 57690 |
rs776568695 | snp | A/C | 0.000610263 | 0.0174573 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086939 | CGTGAAGCAGCCACC[A/C]CCGCCACCGCCCCCG | 57690 |
rs776577942 | snp | C/T | 2.10307e-05 | 0.00324267 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075095 | GTGCTCAGCACTCAC[C/T]TGTTTTGTTTACAAC | 57690 |
rs776587498 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019863 | TTTTTGAAGAAGGGG[A/G]ATGTCAAGATTGCTT | 57690 |
rs776589936 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040825 | AGCTGTAAAATCCCA[G/T]CCGTCCATGCCTCCG | 57690 |
rs776617298 | snp | A/G | 4.46578e-05 | 0.00472514 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102583 | ACTGAGCATGATCCA[A/G]GGAGGGTTCCCGCTT | 57690 |
rs776619452 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106147 | AACAAGCACTTGGGC[A/G]TGGGTTGTGACTGCT | 57690 |
rs776665025 | snp | A/G | 1.66263e-05 | 0.00288321 | missense | TNRC6C | GRCh38.p7 | 17:78067811 | ATGAAATGAACCTCA[A/G]TACCAGCCAGTGGGA | 57690 |
rs776729546 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041841 | CTAGTTTTTATAATA[C/T]ATATTATTTCAGTTA | 57690 |
rs776736912 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022414 | TATGATTTGCTTACT[A/T]CTTCCTTTCTGTAGC | 57690 |
rs776746917 | snp | A/G | 2.46084e-05 | 0.00350765 | missense | TNRC6C | GRCh38.p7 | 17:78091590 | CTTCCCCCCTGGAGC[A/G]GAACCCTAGCAAGCA | 57690 |
rs776764284 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101419 | TTCCCACATTCTCCC[A/G]TCTATTTCTGAGCCT | 57690 |
rs776799918 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011676 | TATGGCTATATACTT[C/T]CATTTATCTTGAGTA | 57690 |
rs776802248 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006379 | AAAGGTTTATGGTAC[A/G]TAGTTGTGTATGAAT | 57690 |
rs776814950 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027759 | TGGCATCATAAGACA[A/C]ATCCCAATGTAAGTG | 57690 |
rs776823145 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78079481 | ACAGCCACCAGTGCA[A/G]CCTCTTAACTCTTCC | 57690 |
rs776835367 | snp | A/G | 1.66114e-05 | 0.00288192 | missense | TNRC6C | GRCh38.p7 | 17:78083153 | TGTTGAACCAGCTCT[A/G]TCAGCTGCAGCTGGT | 57690 |
rs776836448 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078028 | CACACACACACACAC[C/T]GCTTGGAGACATGTC | 57690 |
rs776859609 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010505 | ACATAGAAATATATG[C/T]TTTTCATATGTTTTT | 57690 |
rs776872679 | in-del | -/CTG | 0.000310103 | 0.0124481 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050705 | CTACTGCTGTTAGTA[-/CTG]CTGCTGCTGCCAAGA | 57690 |
rs776916576 | in-del | -/CCAGGT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100866 | TGCAACCTCTGCCTC[-/CCAGGT]CCAGGTTCAAGTGAT | 57690 |
rs776925806 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095992 | GGAGGTCAAGGCTGC[A/C]GTGAGCTGTGATTGG | 57690 |
rs776942557 | snp | C/T | 3.31824e-05 | 0.00407309 | missense | TNRC6C | GRCh38.p7 | 17:78049877 | AGGGGAATGGAGACA[C/T]TGTGAACTCAGCATT | 57690 |
rs776969938 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091322 | CAAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 57690 |
rs776990768 | snp | A/G/T | 0.000167803 | 0.00915835 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098395 | CCCTACCTCCCACAC[A/G/T]CAAGCCTCTCTGTCT | 57690 |
rs777029941 | snp | A/G | 1.72594e-05 | 0.00293758 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086490 | CTATTTTAACTCTTC[A/G]TTCTGTCAACAGGCA | 57690 |
rs777046940 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092563 | AGGGTTTCAATCTTT[C/T]AGGGCTGAAATTGTA | 57690 |
rs777061767 | snp | A/T | 1.67758e-05 | 0.00289614 | missense | TNRC6C | GRCh38.p7 | 17:78067898 | GCAGCTCCTGGGGGA[A/T]CGCCCCCAAAAAAGG | 57690 |
rs777076456 | snp | A/G | 1.72475e-05 | 0.00293657 | missense | TNRC6C | GRCh38.p7 | 17:78050578 | ACAAATACCTCTTCA[A/G]TATCTGGGTGGGTCA | 57690 |
rs777093911 | snp | A/G | 1.65781e-05 | 0.00287902 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098464 | CACGAGGCCACCTCC[A/G]GGGTTAACCAATCCC | 57690 |
rs777147391 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78022591 | CAGCCATATCATCTC[A/G]GTTGCCTGAGTCTGT | 57690 |
rs777166383 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089556 | ATGGTCAGTAGTGGG[A/G]GCTCCTAGCTACCTT | 57690 |
rs777175230 | snp | A/C/T | 3.33618e-05 | 0.00408412 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087105 | CTCGGTGAGTGTCCC[A/C/T]TGGTCTTCAACAGCC | 57690 |
rs777176550 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78060273 | GTTTTATTGATCTTA[A/C]AGCTATCAATTCTGC | 57690 |
rs777196554 | in-del | -/TTCTTCTTCTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78006514 | TTCTTCTTCTTCTTC[-/TTCTTCTTCTTC]TTCTTCTTCTTCTTC | 57690 |
rs777231965 | snp | A/C | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093702 | TCCTGGCAGTGTCCC[A/C]ACTGGGCCTACCATC | 57690 |
rs777242037 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78099706 | ATCATTCTGCCCCTG[A/C]CCCCTCCCAAATCTC | 57690 |
rs777243268 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017238 | AAATATTTCTAAATA[A/C]ATTTTTAAAGAAAAG | 57690 |
rs777266768 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78008711 | TTGTTGTAGTCAACT[C/T]TTTCTTATTTTTCCC | 57690 |
rs777312151 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018023 | GTGTAATTTTCTATT[C/T]GTGAAATCATTTTAA | 57690 |
rs777319363 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78048662 | ATTTTAAAAACATTA[A/G]CGCTCTTTAAAATGG | 57690 |
rs777324413 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029156 | ACTGCATTCTTTCCC[A/G]GTAAATCTGGCAGAG | 57690 |
rs777334393 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063808 | CTATGATGGTCAAAA[C/G]ATAAACAAGAATAAT | 57690 |
rs777343463 | snp | C/T | 1.66076e-05 | 0.00288158 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78067872 | TGCTTCCCAAGAAAG[C/T]ACCTCCTCCTGCAGC | 57690 |
rs777373651 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78094956 | AAGGAGCCGTGTAAG[A/T]TGGCAGAGGACAGGT | 57690 |
rs777383827 | snp | G/T | 1.7423e-05 | 0.00295147 | missense | TNRC6C | GRCh38.p7 | 17:78098375 | AAATCGACGTGGTCC[G/T]CTGGCCCTACCTCCC | 57690 |
rs777387095 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052190 | TCTGGGGTTCTTTTC[A/T]CTCTGGGAGTGTGAA | 57690 |
rs777405166 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009874 | ATGATTTTTAAGTCA[C/T]ATACATCTGAATTTA | 57690 |
rs777409024 | snp | C/T | 9.0138e-05 | 0.00671274 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050628 | GCCAGCAAACACAGG[C/T]TGGGGAGACAGCAAC | 57690 |
rs777437744 | snp | C/G | | | missense | TNRC6C | GRCh38.p7 | 17:78051383 | GCAACACCACACACA[C/G]GGTCGAGACGCCGCC | 57690 |
rs777442376 | snp | C/T | 1.95647e-05 | 0.00312761 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086453 | GTTGAACCATTAGTT[C/T]AACTTACACTTAATT | 57690 |
rs777457167 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081418 | CACTGAGTTGATAGT[A/G]CACAATTATCAATAT | 57690 |
rs777507257 | snp | A/C | 0.0224541 | 0.103551 | intron-variant | TNRC6C | GRCh38.p7 | 17:78087115 | GTCCCATGGTCTTCA[A/C]CAGCCACATCAGGTA | 57690 |
rs777510825 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089815 | ACAGTAAATAAAGAG[A/G]AAGCCTTTCCAAATA | 57690 |
rs777513040 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | TNRC6C | GRCh38.p7 | 17:78079416 | AGTGGCAATCTGGGT[A/G]TGTTTGGCAATAGTG | 57690 |
rs777540223 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78026971 | AAATACTCAGAAGGG[C/T]GAGGCGAGAAAGCTG | 57690 |
rs777597266 | snp | A/G | 1.66029e-05 | 0.00288117 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098419 | TCTGTCTCATGAACT[A/G]TGGAAGGTGCCCAGA | 57690 |
rs777603042 | snp | A/G | 6.21755e-05 | 0.00557529 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78077321 | GCATGCAAAACTTGA[A/G]TTCTTCTAGACAGGT | 57690 |
rs777652585 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035813 | TTCTATTGGTGTATT[C/T]CCGAGGAGTAACCAG | 57690 |
rs777664350 | in-del | -/T | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105114 | GTGTTGTCATTTTGA[-/T]TTTTTTTTTTTTTTT | 57690 |
rs777679751 | snp | A/G | 0.00133798 | 0.0258302 | intron-variant | TNRC6C | GRCh38.p7 | 17:78091424 | AGGCGAATCCTAACC[A/G]CATCTCTCTCTTTAG | 57690 |
rs777706665 | in-del | -/G/GG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090528 | GGAAATACAAGGGGA[-/G/GG]GGGGGGCGCTTGTGC | 57690 |
rs777707135 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039994 | AGTCAGTTATTGCCA[A/G]TGGTGGAAGGGCTTC | 57690 |
rs777707644 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095797 | ACCTGTAATCCCAGC[A/G]CTTTGGGTGGCCAAC | 57690 |
rs777712148 | snp | A/C | 3.53426e-05 | 0.00420357 | missense | TNRC6C | GRCh38.p7 | 17:78049139 | ATGGCACCAATGGCG[A/C]ACTCGTCCAAAGCCC | 57690 |
rs777727141 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071396 | TATCAAAAAGGGTGT[A/G]AGAGCCTTTTCCTAG | 57690 |
rs777730188 | snp | C/T | 1.82487e-05 | 0.0030206 | missense | TNRC6C | GRCh38.p7 | 17:78050213 | GTGAACACATGAACT[C/T]CTGGGCCAAAGCGGC | 57690 |
rs777787857 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025565 | TGTGTGCAGGTTTTT[A/G]TATGAACGTAAAGTT | 57690 |
rs777804030 | snp | A/C | 5.4778e-05 | 0.00523316 | missense | TNRC6C | GRCh38.p7 | 17:78104805 | CCACGCCGCTAACCA[A/C]CCTGCTGCCTGGGGA | 57690 |
rs777905479 | snp | A/G | 1.76021e-05 | 0.0029666 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050337 | AAGGCGAGATAAAGG[A/G]ATTATAGACCAAGGG | 57690 |
rs777932613 | snp | A/G | 1.66004e-05 | 0.00288096 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064742 | TCAGGCTGGGGAGAA[A/G]TGCCTAATGTTCACT | 57690 |
rs777960378 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042566 | CGGTCATTTCACAGA[-/T]TTTTTTTTTTTTTTT | 57690 |
rs777965233 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034503 | GTTCATTGTCCCCCC[A/G]CACCCGTGAGGCTTC | 57690 |
rs777976257 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086252 | GGAGAATTGCTTGAA[C/G]CCGGGAGGCAGAGGT | 57690 |
rs777978567 | snp | A/G | 4.98965e-05 | 0.00499457 | missense | TNRC6C | GRCh38.p7 | 17:78086902 | TCCAGCAGCACCAGC[A/G]CCAGCTGGCCCAGGC | 57690 |
rs777986179 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096091 | GCTGGGATTACATGC[A/G]TGAGCCAGTGCGCAC | 57690 |
rs777989024 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | TNRC6C, TNRC6C-AS1, TMC6 | GRCh38.p7 | 17:78108682 | TGTAGGGACCCCACG[C/G]AAAGACCTCGTGGGC | 57690 |
rs777991262 | in-del | -/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005099 | GTTTATTTATATTTA[-/G]GGGGGTACATTTATG | 57690 |
rs778004695 | snp | A/G | 0.000258771 | 0.0113718 | missense | TNRC6C | GRCh38.p7 | 17:78075172 | TGGACGTGGACAAGC[A/G]TGGGCTGGGAGTGAC | 57690 |
rs778024304 | in-del | -/ATAAAT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091946 | ATAAAATGGTAAAAC[-/ATAAAT]AGAAAATCAAATATA | 57690 |
rs778025231 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090536 | CAAGGGGAGGGGGGC[A/G]CTTGTGCTGGTTATT | 57690 |
rs778025391 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029153 | CCAACTGCATTCTTT[-/C]CCAGTAAATCTGGCA | 57690 |
rs778043052 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78107136 | GTGCGTATGTGCGTC[C/T]GACATACCACTTCCC | 57690 |
rs778067494 | snp | C/G | 1.71366e-05 | 0.00292712 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086813 | AAGCCATGAGTGTCC[C/G]TTCCCACCTAGTTAA | 57690 |
rs778067516 | snp | C/T | 0.000132595 | 0.00814126 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093681 | TGAGAATGACCCTGA[C/T]GTCACTCCTGGCAGT | 57690 |
rs778075464 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78014347 | AGAGAGTTATGATCA[A/G]TGTTACATATGAGAA | 57690 |
rs778081027 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083790 | TAATAATTCTTGAAA[A/G]TTTTGTAGCTTCACA | 57690 |
rs778083875 | snp | C/T | 1.75659e-05 | 0.00296355 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093158 | TCTGTGCAACAGCAG[C/T]AGGTCAGAATGTGCT | 57690 |
rs778086101 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005496 | TCTTTGCTTATTGAT[A/G]TGTAAAAGATTTCTC | 57690 |
rs778088586 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073588 | ACATTTAAATATAGT[C/G]GATTCTTATTTTCTT | 57690 |
rs778091499 | snp | A/G | 0.000165166 | 0.00908603 | missense | TNRC6C | GRCh38.p7 | 17:78104675 | GCTGGCCACTGGAAC[A/G]CCCCGTGCCTGGGTG | 57690 |
rs778101899 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047129 | CATGAGGGAACCCAA[A/G]CTGATGGTAAAATGA | 57690 |
rs778110124 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078138 | CCTTCCACTCACCAG[C/T]GCCCGACTGTGTGAT | 57690 |
rs778111011 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071779 | AATTTCATTAGTGTA[C/T]AGAGTATATTGACAG | 57690 |
rs778136453 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028621 | TAGATGGCCAAGTCC[A/G]TGTTGAGAGACAAAA | 57690 |
rs778173930 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78003861 | TGAGCCCAGGTATTC[A/G]AGACCAGACTAGGGG | 57690 |
rs778201969 | snp | A/G | 1.66565e-05 | 0.00288583 | missense | TNRC6C | GRCh38.p7 | 17:78050899 | CACTTGGGGGATGGG[A/G]AAAAAAATGGATCTG | 57690 |
rs778203960 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097713 | CCCGGACACCGCCAC[C/T]ACCTTGCTCAGTGCC | 57690 |
rs778220734 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042916 | TTTAATTAGCTCAGT[A/G]TGCAATACAGTCCCC | 57690 |
rs778264014 | snp | A/G | | | utr-variant-5-prime, missense | TNRC6C | GRCh38.p7 | 17:78031560 | CAGCCCCAACCTGCC[A/G]GTACCAGTACCAGTA | 57690 |
rs778270833 | snp | A/G | 1.66574e-05 | 0.0028859 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050862 | AGGGGGAGATTGGGC[A/G]GATTCATCGTCTGTC | 57690 |
rs778281735 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78096710 | CTGCTAGCCAGGATA[C/T]GTGCACTGGCAGAGT | 57690 |
rs778282797 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023184 | TATGCGTAGGTTATA[A/C]GCAAATAATAACCTG | 57690 |
rs778293817 | snp | A/G | 1.68513e-05 | 0.00290265 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071209 | CACCATGCTTCCCAA[A/G]ATGAAATGCCCTCAT | 57690 |
rs778358820 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102863 | TTGGGCCTGGCTGGG[C/T]GCAGTAGCTCATGCC | 57690 |
rs778386206 | snp | A/C/T | 0.000265777 | 0.011525 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086951 | ACCACCGCCACCGCC[A/C/T]CCGCCGCACCTGTCT | 57690 |
rs778396340 | snp | A/G | 3.3765e-05 | 0.00410869 | missense | TNRC6C | GRCh38.p7 | 17:78049228 | GTGTGGGGTGTAGCC[A/G]CAGGCTCCAGCTCTG | 57690 |
rs778399839 | snp | A/C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018546 | TGACATGTTTGGGGG[A/C/G]GTGGAGCAAATGGTA | 57690 |
rs778405222 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78062454 | CCAAACAATGTAAAA[C/T]TGATGGTTAACTATT | 57690 |
rs778449160 | snp | C/T | 0.000335247 | 0.0129426 | missense | TNRC6C | GRCh38.p7 | 17:78051155 | TCGGGGGGCCGGTAC[C/T]GGTCAAACAGAAGGA | 57690 |
rs778452405 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78007205 | TCTCTTCTCCTTCTA[C/T]ATCCTCTAAAATACT | 57690 |
rs778483942 | snp | A/G | 1.65641e-05 | 0.00287781 | missense | TNRC6C | GRCh38.p7 | 17:78049610 | ACCTTAACACTGATG[A/G]ACCAAATAACACTAA | 57690 |
rs778500602 | snp | A/G | 7.27326e-05 | 0.00603001 | missense | TNRC6C | GRCh38.p7 | 17:78050725 | GCTGCTGCCAAGAGT[A/G]GCCATGCTTGGAGTG | 57690 |
rs778501273 | snp | C/G | 1.75733e-05 | 0.00296418 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067953 | CTTAACGACGGTACA[C/G]CCTGAAAACCAAAGG | 57690 |
rs778522300 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056686 | TAGCCAGGATGGTCT[C/T]GGTCTCCTGACCTTG | 57690 |
rs778531489 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78093407 | CTATTCCAACCCTGT[A/G]TGAAAACTAGCTTAA | 57690 |
rs778533403 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080492 | ATCGAATTAAGGAAA[A/C]GGATATTGCTGTTTG | 57690 |
rs778541245 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019589 | CCTCATTTAAAAAAC[A/G]AAAGGCAAAAGCTTA | 57690 |
rs778572480 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090678 | TTAGTGCAGGTCCTG[C/G]ACAAATAACCAGGTA | 57690 |
rs778599581 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074388 | AATTTTAGCAAGTAG[C/G]CCAGCTTTACAAGTA | 57690 |
rs778647863 | snp | A/G | 3.31549e-05 | 0.0040714 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78098452 | CAGTACTGCACCCAC[A/G]AGGCCACCTCCAGGG | 57690 |
rs778665251 | in-del | -/AA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051481 | TGTTTCTTTACAAGT[-/AA]AAAAAAAAAAAAAAA | 57690 |
rs778670893 | snp | A/G | 1.81826e-05 | 0.00301513 | missense | TNRC6C | GRCh38.p7 | 17:78050276 | GTGATGGTTCTGGCA[A/G]CCACAATGAAGGAAG | 57690 |
rs778687507 | snp | A/G | 1.65726e-05 | 0.00287855 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78064781 | GAAAACTCTTGGGGA[A/G]AACCATCCTCCCCTT | 57690 |
rs778710126 | snp | A/G | | | | | GRCh38.p7 | 17:78102586 | GAGCATGATCCAGGG[A/G]GGGTTCCCGCTTGGC | 57690 |
rs778714458 | snp | A/G | | | | | GRCh38.p7 | 17:78038237 | GAGGACATGTTTACA[A/G]TGTAAATAGCAAAAG | 57690 |
rs778719328 | snp | A/G | | | | | GRCh38.p7 | 17:78070303 | TAGTTCCTTGAGGAA[A/G]GAAAGCCTGTTTATA | 57690 |
rs778741720 | in-del | -/T | | | | | GRCh38.p7 | 17:78037074 | TTGTCATAATTCACC[-/T]TTTGATTTACATTAA | 57690 |
rs778753502 | snp | A/G | 1.72988e-05 | 0.00294093 | | | GRCh38.p7 | 17:78049711 | GTTGGTATGGGGGCC[A/G]TCATCCCGCCCCACC | 57690 |
rs778767844 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78051982 | CAGAGTAGAGAGATT[C/T]TAAGGTGGCAAAGTC | 57690 |
rs778778538 | snp | A/G | 3.32414e-05 | 0.00407671 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079575 | CAGGACTGAGCAACA[A/G]GATATAGATGCCAGT | 57690 |
rs778795031 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78025443 | AATTTTTTTAAATCA[C/T]GTAATGTTCCATTGT | 57690 |
rs778805087 | snp | C/G | 1.82407e-05 | 0.00301994 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78104833 | GGACCTGCTCAGCGG[C/G]GAGTCCCTGTAGGCT | 57690 |
rs778821924 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067129 | AGGAGGACTACTTGA[A/G]CCCAAGAGTTTGAGA | 57690 |
rs778835008 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078027 | ACACACACACACACA[C/T]CGCTTGGAGACATGT | 57690 |
rs778843032 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105488 | ATATCAAACATGCAA[A/G]TACTTGAATCCAGCA | 57690 |
rs778886352 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089535 | ATGTAAAGAAACCAG[C/G]AGCCCATGGTCAGTA | 57690 |
rs778899764 | snp | C/T | 1.66255e-05 | 0.00288314 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049347 | CAACTCCAATGCTGG[C/T]ATTAATCTTAACCTT | 57690 |
rs778935223 | snp | A/G | 8.3042e-05 | 0.00644314 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093813 | GGTCTCTCTAGACCC[A/G]TTTGGAGATGTCAGG | 57690 |
rs778948539 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065524 | GTAATACCCACACTA[C/T]TTCAGCAGTATTCTT | 57690 |
rs779017273 | in-del | -/CCTG | 0.000105169 | 0.00725076 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077376 | ATGGCCTTTGTTTTA[-/CCTG]CCTTCTAAAAAATGT | 57690 |
rs779048649 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081373 | TTGAGGGTAATTCTC[A/G]CTCTGTAATTGTTCA | 57690 |
rs779056401 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78076358 | CCCAGGGTGAGGCTC[A/G]CGTCTTCATCCTGCC | 57690 |
rs779096044 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78045896 | TAACATAATATCATG[C/T]CATATTTGCTTCAGG | 57690 |
rs779109501 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031898 | ACTTTGCTATTTTCA[A/T]CTTTGCTGCTGAGCA | 57690 |
rs779141993 | snp | A/G | 1.66007e-05 | 0.00288098 | missense | TNRC6C | GRCh38.p7 | 17:78049940 | TGCAAAAGGAAGGAA[A/G]TGGAGGAAATGCTTG | 57690 |
rs779144293 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074750 | AAGAAAGCAACCACT[A/G]AGCCCACCCGAAATG | 57690 |
rs779166062 | in-del | -/AGG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084074 | GGATCACCTGAGGTC[-/AGG]AGTTCGAGATTAGTC | 57690 |
rs779182116 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002415 | CCGACTGTAACAGAA[A/G]AATAGCCTTTGCAGG | 57690 |
rs779189860 | snp | A/G | 0.000116272 | 0.00762382 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086954 | ACCGCCACCGCCCCC[A/G]CCGCACCTGTCTCTG | 57690 |
rs779216878 | snp | A/G | 1.65649e-05 | 0.00287788 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78093708 | CAGTGTCCCCACTGG[A/G]CCTACCATCAACACC | 57690 |
rs779225394 | snp | A/G | 1.65974e-05 | 0.0028807 | missense | TNRC6C | GRCh38.p7 | 17:78093049 | AGTCCTCCCGTAGCT[A/G]TTCCCCATAGCTGGT | 57690 |
rs779229610 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78083714 | TACATATAGTAGATG[C/T]CTTAGAGCATTAGAA | 57690 |
rs779254940 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78016265 | GATTGGGAATGTGGC[C/T]CCTGCACAGAAACTG | 57690 |
rs779258846 | snp | C/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010074 | TTTTTATACAGGCAG[C/G]GTTTCGCCCTGTTGC | 57690 |
rs779298525 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040594 | GGGAGAAAGAAGGAG[C/T]GGAAAACAAAGGCAG | 57690 |
rs779311616 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78020753 | AAAATTGTTAATGAG[G/T]TATTTCTCTTTTTTT | 57690 |
rs779315476 | snp | A/G | 7.56172e-05 | 0.00614841 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092905 | GGAGAGTATTCACTC[A/G]CTTCTTTGTTTCCTA | 57690 |
rs779331843 | snp | C/T | 1.65787e-05 | 0.00287907 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78103497 | GACTCAAGGCAATGC[C/T]GTGGTCCGGTACAGC | 57690 |
rs779337923 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095054 | TGCCAGACAGGAAAA[C/T]TAGCATATTTTGAGG | 57690 |
rs779353650 | snp | A/G | 5.02449e-05 | 0.00501198 | missense | TNRC6C | GRCh38.p7 | 17:78049844 | CTGCCACAGGAAATA[A/G]CAATTCTGGGTTCAG | 57690 |
rs779367901 | in-del | -/ATTA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042361 | CATTCCTTACTGTTT[-/ATTA]GTTACAAACCCTGGC | 57690 |
rs779370107 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78095733 | GAACATCTCTTCACG[C/T]AGAAATTGCTAACCA | 57690 |
rs779370440 | in-del | -/CC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028694 | CCGTATCATGAACCA[-/CC]CCCCAATGTTGACTT | 57690 |
rs779392683 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011327 | TGACCTTTTCTGATC[C/T]ATCTCCTCTGTCCCC | 57690 |
rs779407101 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78106949 | TTTATAGAGGATCAT[C/G]AACTATGCACAAACT | 57690 |
rs779422604 | snp | A/G/T | 3.46238e-05 | 0.00416064 | missense | TNRC6C | GRCh38.p7 | 17:78049811 | GCAATTCTGTGTGGG[A/G/T]ACTGTCCCCAGGTAA | 57690 |
rs779423084 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034323 | CAGCCTCCCAAAGTG[C/T]TGTGATTCCAGGCGT | 57690 |
rs779433780 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78066146 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 57690 |
rs779434076 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78053437 | GAGTTCGAGACCAGC[C/T]TGACCAACAAGGTGA | 57690 |
rs779436510 | snp | A/G | 1.86816e-05 | 0.00305622 | missense | TNRC6C | GRCh38.p7 | 17:78051028 | CCAGGTACAAACTGG[A/G]GGGAGACTTTAAAAC | 57690 |
rs779525728 | snp | A/G | 4.78114e-05 | 0.00488911 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075281 | CTTTCTTGACAAGGT[A/G]TGAATATAGGTGGTT | 57690 |
rs779548021 | in-del | -/TGG | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78042780 | TGGTGGTGGTGCTGA[-/TGG]TGGTGGTGGTGGTGT | 57690 |
rs779555861 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78073425 | TGAGTGCGTTCCTCG[C/T]GCCTTGCCCCAGAAC | 57690 |
rs779567250 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061590 | AGAAGCAGGAGGATC[A/G]CTTGAATCTAGGAGT | 57690 |
rs779569767 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78028341 | GAATTGTTGACACCA[C/G]TGGAACAAGGCAGAC | 57690 |
rs779585928 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78091023 | ACTCTGAGAAGCCTC[A/G]GGACCATGTTTATTC | 57690 |
rs779623222 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041440 | TTTCCTTCTTTATTT[A/G]ATAGACTCTTAACCT | 57690 |
rs779628841 | snp | A/C/G | 8.72173e-05 | 0.00660318 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049719 | GGGGGCCATCATCCC[A/C/G]CCCCACCTGCAAGGC | 57690 |
rs779630162 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065174 | GGCAGCATAGTGAGA[C/T]CTTGTCACTACAAAA | 57690 |
rs779638017 | snp | C/T | 8.31317e-05 | 0.00644662 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050880 | TTCATCGTCTGTCCT[C/T]GGACACTTGGGGGAT | 57690 |
rs779641367 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071760 | TAATTTATAATTAAA[C/T]GTGAATTTCATTAGT | 57690 |
rs779650009 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023686 | TGATACACATCTGTC[A/G]TCCTAGCCACTTGGG | 57690 |
rs779692265 | snp | A/G | 3.32557e-05 | 0.00407759 | intron-variant | TNRC6C | GRCh38.p7 | 17:78079579 | ACTGAGCAACAGGAT[A/G]TAGATGCCAGTGTTT | 57690 |
rs779700783 | snp | A/G | 3.15472e-05 | 0.00397148 | intron-variant | TNRC6C | GRCh38.p7 | 17:78102470 | TTCTCCCCTCTTGTT[A/G]CAGGTTCTGCCTGGA | 57690 |
rs779715452 | snp | A/G | 1.6786e-05 | 0.00289702 | missense | TNRC6C | GRCh38.p7 | 17:78050375 | AGTTGCCAAGGAATG[A/G]TCTTGACCCAAGAGT | 57690 |
rs779742573 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78039310 | CAATTTCAAATCTTG[-/CC]CCCCCCCCCCACTCC | 57690 |
rs779780111 | snp | C/T | 2.04447e-05 | 0.00319717 | missense | TNRC6C | GRCh38.p7 | 17:78091565 | TCCATGGATAACTTG[C/T]CCAGTGCCGCTTCCC | 57690 |
rs779783919 | snp | A/G | 1.68488e-05 | 0.00290243 | missense | TNRC6C | GRCh38.p7 | 17:78091461 | TGAACCCAAACATGA[A/G]TGTCAACAGCATGGA | 57690 |
rs779799903 | snp | C/T | 0.000112788 | 0.00750876 | intron-variant | TNRC6C | GRCh38.p7 | 17:78098324 | AGACTGCATATGCTC[C/T]ATCTCTCTGCCTTTC | 57690 |
rs779803354 | snp | C/T | 3.95507e-05 | 0.00444677 | synonymous-codon, intron-variant | TNRC6C | GRCh38.p7 | 17:78064900 | GGCATTTGGAAGAGC[C/T]GGCGCACCTGTTGCT | 57690 |
rs779830394 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082730 | GCTATGAACATCTGC[A/T]TTTCTGGGATAGGAA | 57690 |
rs779844085 | snp | C/G | | | missense | TNRC6C | GRCh38.p7 | 17:78050849 | CCTGGAGTGCAGGAG[C/G]GGGAGATTGGGCAGA | 57690 |
rs779852218 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081271 | GTTTCAACATAGGAA[G/T]TCTCGGGGGACGCAG | 57690 |
rs779874446 | snp | C/T | 1.65949e-05 | 0.00288048 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78086961 | CCGCCCCCGCCGCAC[C/T]TGTCTCTGCACCCCT | 57690 |
rs779900943 | snp | G/T | 1.75191e-05 | 0.0029596 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067723 | CTGCGTTAGGGACAT[G/T]AATTTGATAAGTTCA | 57690 |
rs779928990 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78037300 | GTCATGTGTGTCTTC[A/G]TTTGTTCATTGAGCA | 57690 |
rs779930204 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78044313 | TGAAAATTTAAGCAT[A/C]ATTTATATTACTAGC | 57690 |
rs779969367 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005981 | AGTTTTTTTCCACTG[C/G]ACCATCACATGTACA | 57690 |
rs779998276 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018503 | CCATTAAATATTTTC[C/T]AAATAAGGAGAGGAT | 57690 |
rs780007578 | snp | C/T | 0.000149477 | 0.00864385 | intron-variant | TNRC6C | GRCh38.p7 | 17:78075305 | GGTGGTTTGTTGTTT[C/T]TGCTTTTTTAACAAG | 57690 |
rs780012933 | in-del | -/AG | 1.73243e-05 | 0.0029431 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083008 | AGTAACTATTTTAAC[-/AG]AGATACAACGGCTAA | 57690 |
rs780030429 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098750 | TAGGTGTGCCGGCAC[A/G]CAGCAGGTTTGCTCT | 57690 |
rs780032603 | snp | C/G | 1.66054e-05 | 0.00288139 | intron-variant | TNRC6C | GRCh38.p7 | 17:78103576 | TTCTCACAGCCACCT[C/G]AGCGCTCCAAGTAGC | 57690 |
rs780077087 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78034508 | TTGTCCCCCCGCACC[C/T]GTGAGGCTTCCCCAA | 57690 |
rs780079961 | snp | A/G | | | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049584 | TGTGTCTTTCAGCGC[A/G]CAACCTCAGAACCTT | 57690 |
rs780096535 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78087032 | ACAGACTCCCGGCCT[A/G]CCTGACCTGCAGACC | 57690 |
rs780101222 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038874 | TACACATATTAACTC[A/T]TTTAATCTTCTCAAG | 57690 |
rs780103239 | snp | C/T | 6.6357e-05 | 0.0057597 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78083097 | CATTGGTCTCAACCC[C/T]GCACTATTAACCTCG | 57690 |
rs780127928 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78036175 | GTTCTTTCAGCTTCG[C/T]ACACGAATTTCTGTG | 57690 |
rs780225076 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082691 | TTTATAGGCTCTCCC[-/C]AAGGGTCGCATTCCA | 57690 |
rs780239240 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78004973 | ATACTAAAAGTTTGC[C/T]TATAAACTTTCATAG | 57690 |
rs780241860 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78056603 | CGAGTAGCTAGGACT[A/G]CAGGTGCCCGCCACC | 57690 |
rs780243090 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78065008 | TTGAATTTTAAAGAT[C/T]AGAGTTTTAGGATAC | 57690 |
rs780262842 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074654 | AGAATACTTGCAGAT[A/G]CAGGACTCGGTGAAT | 57690 |
rs780277966 | snp | C/G | 2.93277e-05 | 0.00382923 | missense | TNRC6C | GRCh38.p7 | 17:78075213 | GGAATGGCCGCCAAG[C/G]CCCTCGGCTGCCGCC | 57690 |
rs780289503 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78100742 | TTTCTGCACCCAGCT[C/T]GAATTTTTCCTCAGA | 57690 |
rs780294972 | snp | A/G | 1.66297e-05 | 0.0028835 | missense | TNRC6C | GRCh38.p7 | 17:78049376 | TTAATCCTAATGCCA[A/G]CCCAGCTGCCTGGCC | 57690 |
rs780296842 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055289 | AGGCCTACACAGGGC[C/T]GGGATCTTCAGTATC | 57690 |
rs780312107 | snp | C/G/T | 3.32165e-05 | 0.00407519 | missense | TNRC6C | GRCh38.p7 | 17:78087088 | CCTTTGCTCCTTACC[C/G/T]TCTCGGTGAGTGTCC | 57690 |
rs780337093 | snp | C/T | 1.70796e-05 | 0.00292224 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093134 | CCCCAGGTAAGACCA[C/T]GCAACACTTCTGTGC | 57690 |
rs780359601 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78007815 | TGGTTTTGATAATTA[A/G]CTCAAACTAGACCAA | 57690 |
rs780362227 | snp | A/G | 1.70519e-05 | 0.00291987 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086615 | AGATTGATTTTTGTC[A/G]TGAGCTATAATTTTC | 57690 |
rs780376885 | snp | A/G | 1.66532e-05 | 0.00288554 | missense | TNRC6C | GRCh38.p7 | 17:78067885 | AGCACCTCCTCCTGC[A/G]GCTCCTGGGGGAACG | 57690 |
rs780425103 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052316 | GACTTGACTGGGGCC[C/G]CTGGAGGGTTGCTGG | 57690 |
rs780427649 | snp | A/G | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105325 | CGCCGGGCGCAGAGC[A/G]GCTCCGCGGCGGGAG | 57690 |
rs780452172 | snp | A/T | 1.85444e-05 | 0.00304498 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086478 | TTAATTATCATACTA[A/T]TTTAACTCTTCGTTC | 57690 |
rs780481218 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78104402 | TTCCATGTGGGGCCG[C/T]TCCCAATACAGAGAA | 57690 |
rs780482360 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78063967 | TTGCAAATGCTGACA[A/G]TTGAATAGGCTTTAA | 57690 |
rs780539897 | snp | A/G | 1.65952e-05 | 0.00288051 | missense | TNRC6C | GRCh38.p7 | 17:78093058 | GTAGCTGTTCCCCAT[A/G]GCTGGTCACGTGCCA | 57690 |
rs780577701 | snp | C/T | 1.71746e-05 | 0.00293036 | missense | TNRC6C | GRCh38.p7 | 17:78050066 | ACCCCAGCCGAAGCA[C/T]CTCTAACGGTGTGAA | 57690 |
rs780592730 | in-del | -/AGAA | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78082436 | ACAGAGCCTTAAAAC[-/AGAA]ACACAGTCTGTCCAT | 57690 |
rs780607365 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78033459 | CGGATCACCTGAGGT[C/T]GAGAGTTCGAGACCA | 57690 |
rs780620028 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78027074 | CAGGAAACCTGCCAA[A/G]GGGGATGGGAAATAG | 57690 |
rs780659436 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78077680 | TGCCCACCCTCTTTC[C/G]TCATGGCAACCAAAA | 57690 |
rs780661413 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102186 | GAGATTCTCGGGCCT[C/T]ATCACCCCCGTCTCT | 57690 |
rs780665319 | snp | A/G | 9.35235e-05 | 0.00683762 | missense | TNRC6C | GRCh38.p7 | 17:78051358 | ACCACCACCACCACC[A/G]CTACCACGAGCAACA | 57690 |
rs780665451 | snp | C/G | 1.66443e-05 | 0.00288477 | missense | TNRC6C | GRCh38.p7 | 17:78049981 | CCTCCTGCTGGTCCT[C/G]GAATACTCGCCTGGG | 57690 |
rs780673426 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78019930 | AGTGAGGATCTGAAA[A/G]GAGTTTATGGCTAGA | 57690 |
rs780705898 | snp | C/T | 3.31923e-05 | 0.0040737 | missense | TNRC6C | GRCh38.p7 | 17:78049922 | ATGGATCCAGCAGTG[C/T]TGTGCAAAAGGAAGG | 57690 |
rs780709222 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78071625 | ACACCTGGGCTCAAG[C/T]GATCTGCCCGCCTCG | 57690 |
rs780727036 | in-del | -/GCT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084840 | CACCATGTTGGTCAG[-/GCT]GCTGGTCTCCAACTC | 57690 |
rs780733669 | snp | C/T | 4.3032e-05 | 0.00463834 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78091573 | TAACTTGCCCAGTGC[C/T]GCTTCCCCCCTGGAG | 57690 |
rs780782866 | in-del | -/TTTC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029727 | TGTACAAAAAATATT[-/TTTC]TTTCTTTATATCCTT | 57690 |
rs780813723 | snp | C/T | 3.3184e-05 | 0.00407319 | missense | TNRC6C | GRCh38.p7 | 17:78083111 | CTGCACTATTAACCT[C/T]GCCAATTAATCCTCA | 57690 |
rs780816209 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C | GRCh38.p7 | 17:78040272 | CAGGTTCAGTGCAGA[C/T]TATGTTTTGCAAGTC | 57690 |
rs780824926 | snp | C/G | 1.72773e-05 | 0.00293911 | intron-variant | TNRC6C | GRCh38.p7 | 17:78067747 | AAGTTCATGTTTGCT[C/G]TGTTTCTAGCTTCAA | 57690 |
rs780830218 | snp | C/T | 1.91272e-05 | 0.00309245 | intron-variant | TNRC6C | GRCh38.p7 | 17:78092902 | ACTGGAGAGTATTCA[C/T]TCGCTTCTTTGTTTC | 57690 |
rs780849118 | snp | C/T | 8.29552e-05 | 0.00643978 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78103470 | GCCTCTTATCACATT[C/T]CACCTGAATCTGACT | 57690 |
rs780858252 | snp | A/G | 1.66374e-05 | 0.00288417 | missense | TNRC6C | GRCh38.p7 | 17:78049393 | CCAGCTGCCTGGCCT[A/G]TACTTGGACATGAAG | 57690 |
rs780865396 | snp | C/G | 1.71616e-05 | 0.00292925 | missense | TNRC6C | GRCh38.p7 | 17:78049819 | GTGTGGGGACTGTCC[C/G]CAGGTAACCCTGCCA | 57690 |
rs780880829 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78090618 | ACTCTTTACTTCAAC[A/C]TTCTTTTCATTGTCC | 57690 |
rs780894774 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78005653 | CCATACTCCAAGCCT[C/T]TTCCTTTTATACCTG | 57690 |
rs780925340 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101701 | AAGTATCCCTTATGG[G/T]AGATAAAGGGATGGG | 57690 |
rs780927272 | snp | A/G | 1.7327e-05 | 0.00294333 | intron-variant | TNRC6C | GRCh38.p7 | 17:78083005 | ACAAGTAACTATTTT[A/G]ACAGAGATACAACGG | 57690 |
rs780973880 | snp | A/G | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78011236 | AGAGAAGAAATAGAT[A/G]AGTGTTGGCATATAT | 57690 |
rs781006037 | snp | A/G | 3.57686e-05 | 0.00422883 | intron-variant | TNRC6C | GRCh38.p7 | 17:78077143 | GGTGCTTTGTCTGCT[A/G]ATGGACACTGCACAC | 57690 |
rs781034927 | snp | A/T | 1.65682e-05 | 0.00287817 | missense | TNRC6C | GRCh38.p7 | 17:78087069 | CAGCAGTCTTCACCC[A/T]ACACCTTTGCTCCTT | 57690 |
rs781038737 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085672 | AAAGTGCCCACAAAT[A/C]TGCATTTCAGGTTCT | 57690 |
rs781095207 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78055181 | CATTGTACAGCTTCA[C/T]AAAAGTATTTTTTAT | 57690 |
rs781108069 | snp | A/G | 1.66228e-05 | 0.0028829 | missense | TNRC6C | GRCh38.p7 | 17:78098412 | AAGCCTCTCTGTCTC[A/G]TGAACTATGGAAGGT | 57690 |
rs781114992 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78017955 | AGGAGCTTTCTGAAT[A/C]CCTAAATTAGGTTAT | 57690 |
rs781126271 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78089988 | GCATTCTGAAGGCCA[A/G]GTTGAAGCCCTGACA | 57690 |
rs781136024 | snp | A/C/G | 0.000486121 | 0.0155828 | missense | TNRC6C | GRCh38.p7 | 17:78051380 | CGAGCAACACCACAC[A/C/G]CAGGGTCGAGACGCC | 57690 |
rs781141306 | snp | C/T | 0.000102234 | 0.00714888 | missense, intron-variant | TNRC6C | GRCh38.p7 | 17:78097751 | GTTCTGCAGGGTCCT[C/T]CCCGCCATCATCTCA | 57690 |
rs781173288 | in-del | -/AC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78078013 | AGGGATGAGGTTGAC[-/AC]ACACACACACACACC | 57690 |
rs781185484 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024320 | GTATTTCCATTTTTT[A/T]TTAATAGGCTGTATT | 57690 |
rs781193694 | snp | A/G | 9.96231e-05 | 0.00705703 | missense | TNRC6C | GRCh38.p7 | 17:78093068 | CCCATAGCTGGTCAC[A/G]TGCCAAATCTGACAG | 57690 |
rs781234417 | snp | A/G | 1.67161e-05 | 0.00289098 | missense | TNRC6C | GRCh38.p7 | 17:78050533 | GCTTCAAACTCAGGG[A/G]GGAAGAACGATGGGT | 57690 |
rs781258980 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78047703 | GAGAAGAAAATATTT[C/T]ATTGCAGTTTATTTG | 57690 |
rs781264710 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78061185 | AAAGCAGTAGTATTT[G/T]AAGGATCATTTTTAA | 57690 |
rs781266669 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067176 | AGTGAGACCCCATCT[C/T]TATTAAAAAGAAAAA | 57690 |
rs781305979 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78038401 | CCTTGTGGCTGGGTG[C/T]GGTGGCTCACGCATG | 57690 |
rs781306812 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78101048 | CCCAAAATGCTGGGA[C/T]TACAGGCGTGAGCCA | 57690 |
rs781314089 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102405 | ACTTCAGCACAATAA[C/G]AAGTGGGGAGGGCCG | 57690 |
rs781318227 | snp | A/C | 3.33545e-05 | 0.00408364 | intron-variant | TNRC6C | GRCh38.p7 | 17:78064713 | TCTACCCCTTGGAAC[A/C]TTTTTCAGTTTCATC | 57690 |
rs781321722 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78059673 | GGCAACCTAGTGAGA[A/C]CCACGTCTCTACAAA | 57690 |
rs781348935 | snp | G/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78054779 | GTACACTACTATACA[G/T]TACTGCAGACTACTG | 57690 |
rs781365953 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78075623 | TCCCTTTGGAAATTA[C/T]GTGTTAGATGTTTAT | 57690 |
rs781389149 | snp | A/G | 0.000100125 | 0.00707478 | intron-variant | TNRC6C | GRCh38.p7 | 17:78097866 | TAGTGTTGCAGGTAC[A/G]CGCCTGGCCTCTAGA | 57690 |
rs781398960 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78104241 | GACACTGACCCTAAA[C/T]GAGCCCACATTTAAT | 57690 |
rs781403556 | snp | A/G | 1.72169e-05 | 0.00293396 | missense | TNRC6C | GRCh38.p7 | 17:78050074 | CGAAGCACCTCTAAC[A/G]GTGTGAATGGGGAAT | 57690 |
rs781422317 | snp | C/T | 6.90489e-05 | 0.00587534 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78051213 | ACCCTCTCCACCGTC[C/T]ATTCGCCGCAAAATG | 57690 |
rs781442264 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78097035 | TAGGACAGATGTCTC[C/T]TAATTATTCCTGTAT | 57690 |
rs781461499 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78080059 | TAGATTTTCAGTTAT[A/G]TTTAATATTCAGAAT | 57690 |
rs781464498 | snp | A/G | 0.000102148 | 0.00714588 | missense | TNRC6C | GRCh38.p7 | 17:78104657 | GGCCTGGTACGCAGC[A/G]ACGCTGGCCACTGGA | 57690 |
rs781470436 | snp | A/C | 1.66352e-05 | 0.00288398 | missense | TNRC6C | GRCh38.p7 | 17:78086892 | CAGCAGCAGATCCAG[A/C]AGCACCAGCGCCAGC | 57690 |
rs781499768 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78035924 | ATTTTCATTGTACTT[C/T]AATCTGTCACTTTAA | 57690 |
rs781505548 | snp | A/G | 6.7643e-05 | 0.00581523 | missense | TNRC6C | GRCh38.p7 | 17:78104516 | ACTACCATCCTGGCC[A/G]AGTTCGCTGGTGAAG | 57690 |
rs781510610 | snp | C/T | 0.00012665 | 0.00795669 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78050745 | TGCTTGGAGTGGGGC[C/T]GCAAATCAGGAGGAC | 57690 |
rs781512567 | snp | A/C | 8.95215e-05 | 0.00668975 | intron-variant | TNRC6C | GRCh38.p7 | 17:78071193 | GTAGTTTACTGCTAC[A/C]CACCATGCTTCCCAA | 57690 |
rs781514988 | in-del | -/TAA | 1.65965e-05 | 0.00288062 | cds-indel | TNRC6C | GRCh38.p7 | 17:78050930 | ATGGGATGCTGACAG[-/TAA]TAATAGGTCAGGGTC | 57690 |
rs781595235 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78043228 | AGTGGGCTGGGCTGG[A/G]CTGGGCACACTCCCT | 57690 |
rs781621596 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78074607 | CAGAAACAGTGTCTG[C/T]TTTGCACAGTATTGT | 57690 |
rs781641171 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78018595 | ACAACGAGTTTGAGC[C/T]CTTATTTACCGTGCT | 57690 |
rs781642363 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78031191 | TCTGGAGGTTGGCAC[C/T]AGGTGTCTGGGCTCT | 57690 |
rs781650766 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78041958 | TTGTCCACACTTTCA[-/T]TATCTGATTAAATCT | 57690 |
rs781652213 | snp | C/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78102986 | TGTATTTTTATAACA[C/T]TTTTTAAAAGAGTCG | 57690 |
rs781678376 | snp | C/T | 1.73948e-05 | 0.00294908 | intron-variant | TNRC6C | GRCh38.p7 | 17:78086636 | TATAATTTTCCCTGA[C/T]AGAAGAGACGCTAAT | 57690 |
rs781705382 | snp | C/T | 3.65858e-05 | 0.00427686 | synonymous-codon | TNRC6C | GRCh38.p7 | 17:78049119 | CAAGAAGACAAATGG[C/T]AATAATGGCACCAAT | 57690 |
rs781735128 | snp | A/G | 1.7351e-05 | 0.00294537 | intron-variant | TNRC6C | GRCh38.p7 | 17:78093150 | GCAACACTTCTGTGC[A/G]ACAGCAGCAGGTCAG | 57690 |
rs781742093 | snp | G/T | 1.8253e-05 | 0.00302096 | missense | TNRC6C | GRCh38.p7 | 17:78050207 | CTGGTGGTGAACACA[G/T]GAACTCCTGGGCCAA | 57690 |
rs781744883 | snp | C/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78052798 | GCCACATCAGGAATC[C/G]TTTATGGATCCTCAA | 57690 |
rs781762527 | snp | A/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78030196 | GCTCTGTCACCCAGC[A/C]TGGAGTGCAGTGGCA | 57690 |
rs781778728 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78086665 | ATTGATGAACTATTA[A/G]ATGATCATTGATTTT | 57690 |
rs796082705 | snp | C/G | | | upstream-variant-2KB, intron-variant | TNRC6C | GRCh38.p7 | 17:78002690 | TTGAGGCCAGGAGTT[C/G]GAGACTAGCCTGGAC | 57690 |
rs796085046 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | TNRC6C | GRCh38.p7 | 17:78106266 | ATTAAAAAAAAAAAA[-/A]GACTTCCGTCGTAAA | 57690 |
rs796092141 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78085854 | TTTGTTTTTTTTTTT[-/T]AAGTTTCAGTTTGTA | 57690 |
rs796099378 | in-del | -/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78067031 | AGGATGAGATACAGA[-/T]TTATGAAGCATCCCA | 57690 |
rs796100672 | in-del | -/A | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106069 | AGAAAAAAAAAAAAA[-/A]CTGTTGTTGAACTGT | 57690 |
rs796106248 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78081871 | CTGTTACCTGTGAGT[A/T]CTGATAGGAAGGACA | 57690 |
rs796278064 | snp | A/C | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78106873 | ATGGTTTTATCAAAA[A/C]AAAAAAAATACAAAA | 57690 |
rs796308963 | snp | G/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010246 | TTTGCAGTGAGGTAT[G/T]AAACTTTACCATGCG | 57690 |
rs796428171 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087484 | GTTTTGCCGCTGCCA[-/A]TAATACTCTCAGTAT | 57690 |
rs796537980 | snp | A/G/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010080 | TACAGGCAGGGTTTC[A/G/T]CCCTGTTGCCCAGGT | 57690 |
rs796566253 | snp | C/T | | | intron-variant | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78010256 | GGTATTAAACTTTAC[C/T]ATGCGTTCAGTTTGT | 57690 |
rs796566481 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNRC6C, LOC107985010 | GRCh38.p7 | 17:78009477 | TTTCATACAAAAAGC[C/T]CAAAGTTAATCTTAC | 57690 |
rs796604621 | in-del | -/C | | | utr-variant-3-prime, intron-variant | TNRC6C, TNRC6C-AS1 | GRCh38.p7 | 17:78108260 | AGGCTGGCCCCCCCC[-/C]ACCCATGGGGAAGGT | 57690 |
rs796676635 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78098240 | TTTGCCTATCACACA[A/G]TCTGCTGGTGTTAGA | 57690 |
rs796742561 | snp | A/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78087273 | AAGGCTTTTTAATTT[A/T]AAAAAAATTTTTTAA | 57690 |
rs796804267 | in-del | -/C | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029343 | TGCCATGTGATAGAA[-/C]CTTTTGCTCCTAGGC | 57690 |
rs796848835 | in-del | -/A | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78084283 | AGACTCCGTCTCAAG[-/A]AAAAAAAAAAAGAAA | 57690 |
rs796852130 | in-del | ACACA/T | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78029815 | AAACCTAGACACACA[ACACA/T]ACACACACACACACA | 57690 |
rs796908167 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78088971 | TTACTTTTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGATAGAGTCTTGC | 57690 |
rs796935047 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78092383 | CTGTGTTCTTCCGTA[A/G]TGAGGGTTTCAGACT | 57690 |
rs796938914 | in-del | -/GT | | | utr-variant-3-prime | TNRC6C | GRCh38.p7 | 17:78105635 | CGTGTTGAAACAGAA[-/GT]GTGTGTGTGTGTGCA | 57690 |
rs796959306 | snp | A/G | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78023929 | AGCCTGGCCGACATG[A/G]TGAAACCCCATCTCT | 57690 |
rs796998965 | multinucleotide-polymorphism | CT/TC | | | intron-variant | TNRC6C | GRCh38.p7 | 17:78024451 | GCTCACTGCAAGCTT[CT/TC]CCTCCCAGGTTCACG | 57690 |