SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11400 | snp | C/T | 0 | 0 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77097740 | TGAGGATGGGAAAAC[C/T]GAGACCACTTTTGAA | 23077 |
rs383659 | snp | G/T | 0.188631 | 0.242351 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77063964 | TTCTGAGGATTAACC[G/T]AAGCAATTTTTACCA | 23077 |
rs445080 | snp | C/T | 0.11228 | 0.208646 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77046882 | GGCACCAATCTGCAG[C/T]GTGATTTGGAGCAGG | 23077 |
rs624575 | snp | C/T | 0.355525 | 0.226637 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77048683 | AATACCATCTACTCG[C/T]AGATTGTAAAAATGG | 23077 |
rs670513 | snp | A/T | 0.354881 | 0.226936 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050023 | CTCTTTTTTTTTTTT[A/T]AACTGATGCGTAATA | 23077 |
rs687532 | snp | C/G | 0.340559 | 0.233022 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77046925 | GGGTGGGGGAGAGTG[C/G]GCAGGATGGGGACAC | 23077 |
rs696779 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77067440 | CTAATATCTAAAAAG[G/T]TCATGTATAtaataa | 23077 |
rs696780 | snp | A/G | 0.205723 | 0.246048 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77067114 | AACACAGAACCCAAA[A/G]TCATATAGGAAGATA | 23077 |
rs700359 | snp | A/G | 0.449726 | 0.150364 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77069016 | AAACAAGTAAAGCTA[A/G]GGGAGCCACAATAAA | 23077 |
rs727839 | snp | C/T | 0.347253 | 0.230308 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77219237 | GACTCATTGGAGGAG[C/T]AGGTTTCAAGCGTGG | 23077 |
rs851507 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77058138 | agccactgcgcccgg[C/T]cTCAATCAATGTTTA | 23077 |
rs851508 | snp | A/G | 0.202035 | 0.245356 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77059058 | GCATCACCAAAATGC[A/G]GATTTTTTTTTTTTT | 23077 |
rs851509 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77069398 | gaggccgaggcgggc[A/G]gatcatgagatcagg | 23077 |
rs851512 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77049192 | CATGCTTGGAGGGAG[G/T]GGGTGATGTGCTGGA | 23077 |
rs851513 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77049979 | TCCTGAAGATCTTTC[C/G]AAATCAGCACACAGA | 23077 |
rs851514 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77052998 | cagaaattagccagg[C/T]gtggtggtgaggacc | 23077 |
rs861142 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055066 | aagaggtcacccaag[A/G]taaggaagtatttat | 23077 |
rs864850 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77057938 | CGTCTCCTGGCTTCA[C/T]GCCATTCTCCTGACT | 23077 |
rs866451 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77063473 | ctgagacaggagaat[C/T]gcttgtacctgcagg | 23077 |
rs927852 | snp | C/T | 0.489434 | 0.0719116 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77097196 | TGGCCATCATAATAT[C/T]AGAATTTATCTGTTT | 23077 |
rs927967 | snp | G/T | 0.4944 | 0.0526182 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228036 | ATATATTTTAATTCT[G/T]CCACTGCTGCTGATA | 23077 |
rs957259 | snp | A/G | 0.421051 | 0.182323 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77091129 | TATTAGAAAATAGAT[A/G]ATTTTACCAAGGGAC | 23077 |
rs959810 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77091186 | ATGTACATAAGCTTA[A/G]AGAAGTGGTGAGTAA | 23077 |
rs961590 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77281786 | TTATGATCACACTTA[G/T]TCATGAAATAATAAA | 23077 |
rs1041242 | snp | A/G | 0.200801 | 0.245111 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77194037 | CTATGAATATCAAAT[A/G]CTTGAGAAATTAAAT | 23077 |
rs1178626 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77069652 | acgaggtcaggagat[C/T]gagaccatcctggct | 23077 |
rs1178627 | snp | C/T | 0.354881 | 0.226936 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072954 | tttcatcttgtttac[C/T]tctttcatcatttat | 23077 |
rs1178628 | snp | A/G | 0.109814 | 0.206997 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074985 | aggccaatgctggca[A/G]actgcttgagcccag | 23077 |
rs1340530 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77128130 | TCTCTGTGTATTCAT[A/G]TAGGTTTGCATATAT | 23077 |
rs1340531 | snp | G/T | 0.224116 | 0.248656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056859 | CAGGTTCCACATGAA[G/T]GAGAAGGGAAGAAAC | 23077 |
rs1473756 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77097146 | TAATATTTTTTAAAA[C/T]ATGCTACATGAAAGT | 23077 |
rs1538849 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056101 | ACGCTCTGTGTTTGg[G/T]gtgtgtgtgtgtgtg | 23077 |
rs1571296 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77271082 | AAAAGTATGATTAAG[G/T]AGTGAGAATATAAAA | 23077 |
rs1633532 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071115 | GTGGTCTTAAATTAA[G/T]CTATCGGAACACCAA | 23077 |
rs1633533 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071275 | TGTGTGcacacgcac[A/G]cacacacacacacac | 23077 |
rs1770574 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77108910 | gggtttcactgtgtt[A/G]gccaggatggtcgac | 23077 |
rs1770575 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77108917 | actgtgttagccagg[A/C]tggtcgacctcgtga | 23077 |
rs1773244 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071273 | CGTGTGTGcacacgc[A/G]cgcacacacacacac | 23077 |
rs1934738 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77089647 | CCAGATCATGTAACT[C/G]TTTTTTTTTTTTTTT | 23077 |
rs1969954 | snp | C/T | 0.44638 | 0.154709 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77193854 | TACGGAATACCTAGT[C/T]TGCTGGTGTTCTAGT | 23077 |
rs2025907 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77242639 | TCTATTTTCTTACTC[A/G]TTTATGCTCATTATC | 23077 |
rs2027406 | snp | A/G | 0.419456 | 0.183806 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130183 | TGGTTCAAAATAACC[A/G]TTTATCATAATATTT | 23077 |
rs2031804 | snp | A/T | 0.495291 | 0.0482933 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77241241 | GGAAATAAAGGAACA[A/T]TGAATCGTGCATTGA | 23077 |
rs2031805 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77213464 | ttgagacagagcctc[A/G]ctctgtcatccaggc | 23077 |
rs2039872 | snp | A/G | 0.192401 | 0.243274 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77109257 | aatagtctcaagatg[A/G]aactgctccacctca | 23077 |
rs2039873 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77110915 | TTAGGCCCCTAGAAC[A/G]CTTGAAATTATGCCA | 23077 |
rs2073840 | snp | C/T | 0.419456 | 0.183806 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77065456 | TTGTCCTTCTCAGGC[C/T]GCCCTCCTAGAAATA | 23077 |
rs2153504 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77127662 | CTATTTAATACAATT[C/T]TATCTTGCATAATGT | 23077 |
rs2153506 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77077603 | AGAAACTAAGGTTAA[C/T]ACAGGTTAAGGGATT | 23077 |
rs2153507 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77091740 | CTTTTTTTTTTTAAA[C/T]AGAAGGGGTCTTGCT | 23077 |
rs2153508 | snp | C/T | | | missense | MYCBP2 | GRCh38.p7 | 13:77096455 | CAATGCTATTGTAAC[C/T]TTGTCCACCAGCATA | 23077 |
rs2185468 | snp | A/C | 0.352721 | 0.227922 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77092041 | TTCTGACGAGTAATC[A/C]ACACAGTTGGGGAGG | 23077 |
rs2274547 | snp | A/G | 0.323861 | 0.23884 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77164529 | CTAATTCTTTTTCCA[A/G]TTGGATGACTCCCTA | 23077 |
rs2274548 | snp | A/G | 0.352721 | 0.227922 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165526 | TACATAACTTAAATA[A/G]ACTTGCGGCGGGGAG | 23077 |
rs2274549 | snp | C/T | 0.158302 | 0.232576 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165532 | ACTTAAATAGACTTG[C/T]GGCGGGGAGCGTTCC | 23077 |
rs2275561 | snp | A/G | 0.113075 | 0.209169 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77081413 | AGAGCCGTAAATCAC[A/G]TTTGCTTTCTTACCC | 23077 |
rs2275562 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77126656 | ATCTTTAGTTATGTG[G/T]TTTTTTTATATTGAC | 23077 |
rs2277418 | snp | A/G | 0.186737 | 0.241863 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77078946 | GCTTCAGAACTTACA[A/G]TGGTTTCTCATGACC | 23077 |
rs2285383 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77051549 | AAGTTTCACTGCACG[G/T]TTAAGAAACTAAGAA | 23077 |
rs2285384 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77051665 | ATAATATATATGAAA[C/T]AATGTGAAAAATTAT | 23077 |
rs2285385 | snp | A/G | 0.124144 | 0.21601 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77052275 | GCAATCATGGCTCCC[A/G]ACAGCCTCAACCTCT | 23077 |
rs2285386 | snp | C/T | 0.187999 | 0.24219 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77058335 | ACAGGGCAGACAGTG[C/T]TCTTCGTTTTTAACA | 23077 |
rs2285387 | snp | A/G | 0.49655 | 0.04139 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77058910 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 23077 |
rs2285388 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77061110 | AGTTTAATCAGTTGG[C/T]ACGGTTTAATCTTTT | 23077 |
rs2285389 | snp | A/G | 0.493154 | 0.0581045 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77061392 | TCAATAATAATAATG[A/G]CTTTCATTTAAGCAC | 23077 |
rs2296854 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77161652 | TCCTCCGCACCCTTG[A/G]CACTTGATTTGTTTT | 23077 |
rs2296855 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77162184 | CAAGAAGCATCCATG[A/G]GTGATTTGCCAAAGA | 23077 |
rs2301580 | snp | C/T | 0.0845197 | 0.187393 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055795 | ATGAACACTCTTTAG[C/T]AGAATCATTTATTAA | 23077 |
rs2301581 | snp | A/G | 0.0724097 | 0.175959 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055819 | TTATTAACCAACTCA[A/G]CAAACACTTAGCATG | 23077 |
rs2328998 | snp | G/T | 0.125182 | 0.216612 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77053409 | TGTCCGGATTGGGAA[G/T]AAACAAACTGAGTCA | 23077 |
rs2328999 | snp | A/G | 0.353587 | 0.22753 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77112373 | aaatatatattatat[A/G]ttatataaataaaat | 23077 |
rs2329026 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77154261 | CATGTCAGATTTATC[C/T]AATTTAGAAACTTTC | 23077 |
rs2329027 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276862 | TTGGGACCAGTCTGG[A/G]CAACTTAGACCCCTA | 23077 |
rs2329028 | snp | A/C | 0.450231 | 0.149691 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276667 | TCTACCAAAAAAAAA[A/C]CCCCCAAAAAATCCC | 23077 |
rs2329029 | snp | A/C | 0.445592 | 0.155704 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77208161 | tttaaagaggaaaag[A/C]gagcaggaggagaaa | 23077 |
rs2428006 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77052347 | aggatcataggtgca[C/T]gccaccacacccggc | 23077 |
rs2487755 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77052510 | AATCCATTTGAGAGT[C/T]GAAATAGCTTTAggc | 23077 |
rs3038650 | in-del | -/TT | 0.405603 | 0.195673 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77234844 | AAATGGTAATATAAC[-/TT]AATATTATTACCTTA | 23077 |
rs3742103 | snp | C/T | 0.149379 | 0.228857 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77166574 | GGTCAACAGGCAAAG[C/T]GACATGAATACAGAT | 23077 |
rs3752990 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77166447 | ATATCCTGAATTCTG[A/G]ACAGTTCTGACAGGA | 23077 |
rs3752991 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77212319 | TTATAAATATTTGGT[A/C]CAAATTCTTACATAT | 23077 |
rs3753040 | snp | A/C | 0.00566454 | 0.0529168 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77095629 | AAAAATCAAACTAAT[A/C]TTTTCTGACTTACAT | 23077 |
rs3825499 | snp | G/T | 0.15698 | 0.23205 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77224761 | CACACTTAAAAATTC[G/T]TATAAATGCCATTTA | 23077 |
rs3832881 | in-del | -/A | 0.122259 | 0.2149 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77166314 | CACATAAAACAGAAG[-/A]AAAAAAAAACTTACC | 23077 |
rs3837533 | in-del | -/A | 0.138546 | 0.223781 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77048861 | ACCACTGAGTTCTCT[-/A]AAAGTGTTTCATTGT | 23077 |
rs3841487 | in-del | -/AT | 0.0588605 | 0.161139 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77068974 | AGTTAATTCTCCATC[-/AT]ATGTCATTCTCTTAA | 23077 |
rs3861128 | snp | C/T | 0.491263 | 0.0655142 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77158198 | ATTTCTCCGTAAAGG[C/T]CTATCTGAAAGTATC | 23077 |
rs3889340 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77184844 | TGGTTCTTTTCCTCT[C/T]TCCCTCTCTCAGAAT | 23077 |
rs4052542 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77199742 | cagttaggctgctgg[A/G]gggtcaggggtcagg | 23077 |
rs4267189 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77197035 | atgaagtgtagtgtc[A/G]tgggggacaagagaa | 23077 |
rs4465498 | snp | A/G | 0.494187 | 0.0535994 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77141726 | CAGTGGGCAGGGATC[A/G]CGCCACTGCATTCCA | 23077 |
rs4470045 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77081088 | TTTGAGAGACCCTGG[A/G]AGAATTGATCAGCAG | 23077 |
rs4489888 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77093953 | TTTCACGTTTTACAA[C/T]TTGATTCTTTCCTTT | 23077 |
rs4594140 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210856 | ACCTAGTATGCACCT[C/T]TGTAGTATTAGCATC | 23077 |
rs4594141 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210931 | TTCTCCAGGGTGACA[C/T]AGAAAGCAAGTTGTG | 23077 |
rs4884059 | snp | C/T | 0.495213 | 0.048687 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77199447 | gatcaaactgcaagg[C/T]ggcagcgaggctggg | 23077 |
rs4884060 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243655 | TCATCCCTTAAACAA[C/T]GTCATATTGTCAGTT | 23077 |
rs4884061 | snp | A/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77277445 | AAAATCCTCAGCTTG[A/T]TTCAATGACCAGCAT | 23077 |
rs4884062 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77277644 | TAAACCAGCAGTGTA[C/G]TCCTCAAACCAGCAT | 23077 |
rs4885442 | snp | A/G | 0.494442 | 0.0524218 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77147013 | CAGATTATGGAATAG[A/G]TCCCCAATGGAATGC | 23077 |
rs4885443 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77148205 | TTTTAAAAAATGAGA[C/T]AAATATTTATTTCGG | 23077 |
rs4885444 | snp | C/T | 0.175897 | 0.238765 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77176766 | ATTTTCCCATACATA[C/T]GAAAGAAAAAGTTGG | 23077 |
rs4885445 | snp | C/T | 0.428287 | 0.175254 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77177757 | ACTTACATCATCAAC[C/T]AACACCTCTAATTCA | 23077 |
rs4885446 | snp | C/T | 0.446118 | 0.155041 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77199395 | cggagggtcctacgc[C/T]catggagtctcgctg | 23077 |
rs4885447 | snp | A/G | 0.49533 | 0.0480965 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243545 | TTGAACCTAGAAGGC[A/G]GAGGTTGCAGTGAGC | 23077 |
rs4885448 | snp | C/G | 0.495708 | 0.0461266 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77302491 | GAAGACAAAAATAAA[C/G]ATGTTTTTAGATCCA | 23077 |
rs4885449 | snp | G/T | 0.495596 | 0.0467178 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303282 | cggttgcagtgtgcg[G/T]agatcacaccactgt | 23077 |
rs4885450 | snp | A/G | 0.495559 | 0.0469148 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303390 | aattggcatacatac[A/G]gaaacatatccaaca | 23077 |
rs4885451 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77313291 | cctaggattccacct[C/T]aagaaattagaacag | 23077 |
rs4885452 | snp | A/G | 0.202035 | 0.245356 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315120 | GAAAATCTGAATAAC[A/G]CTCTAACTATTAAAG | 23077 |
rs4885453 | snp | C/T | 0.448963 | 0.151372 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77318853 | gaatcagactgaaca[C/T]gccaccctcctttcc | 23077 |
rs5804891 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77057353 | CTTATATAAAGTAAG[-/C]TAGGTTAGGAAAAAA | 23077 |
rs5804892 | in-del | -/A/AA | 0.303688 | 0.244167 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77092081 | GAAAAAAAAAAAAAA[-/A/AA]CCTCATTTGGATATA | 23077 |
rs5804893 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186803 | GTTTATAGATTCAAT[-/T]TTTTTTTTTTTTTTT | 23077 |
rs5804895 | in-del | -/T/TTTTTTTTTTTT | 0.420096 | 0.183214 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276839 | TTTTTTTTTTTTTTT[-/T/TTTTTTTTTTTT]GGAGAGATAGGGGTC | 23077 |
rs6562983 | snp | C/T | 0.449853 | 0.150196 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77143004 | cacagaaACCCCTTT[C/T]CTTGAGGAGCATCAG | 23077 |
rs6562984 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77147295 | CTGAGGAAGGGTTTA[G/T]GCAGGCTTCAATTGT | 23077 |
rs6562985 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174930 | tatattatatatata[A/T]aatatatatatattt | 23077 |
rs6562986 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174931 | atattatatatatat[A/T]atatatatatatttt | 23077 |
rs6562988 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77279236 | AGTAAAAAGATTTTA[C/T]AAGGAGCTTTTCGTC | 23077 |
rs7317131 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77273990 | ACTACTTGTCATACT[C/T]ATTTTACCTTTTAGA | 23077 |
rs7317696 | snp | A/G | 0.102726 | 0.202016 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77321777 | TAAGTATCTGCCTTT[A/G]TATCTTGCACTTCCA | 23077 |
rs7317973 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210741 | AAATAGAATGAATTC[A/T]ATACAATATAAACAG | 23077 |
rs7319080 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77116206 | TCAGTATAAACAAAG[C/T]TGAGTAAATATGGTC | 23077 |
rs7319081 | snp | A/T | 0.354665 | 0.227036 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77116207 | CAGTATAAACAAAGT[A/T]GAGTAAATATGGTCT | 23077 |
rs7319795 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77177490 | gggattacaggcgtg[C/T]gttgtatttttcgta | 23077 |
rs7320950 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77142499 | TGTAAAGTACCTCTT[C/T]ACCTCCACTGCCAAA | 23077 |
rs7322722 | snp | A/G | 0.346147 | 0.230772 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77305241 | accaatatctcctat[A/G]aacatagaagcaaaa | 23077 |
rs7323354 | snp | A/G | 0.030665 | 0.119967 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77220471 | TCATTCTGGCAATAT[A/G]ACACATTAAATAAAG | 23077 |
rs7323733 | snp | C/T | 0.450357 | 0.149522 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77086911 | TCAAATTCATCACTT[C/T]ATATTTCTTCTTACA | 23077 |
rs7323979 | snp | C/T | 0.040671 | 0.13668 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77321004 | TTTTATATGAAGTGA[C/T]GGAAACAGTCTATAC | 23077 |
rs7324014 | snp | C/T | 0.438806 | 0.163867 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77322955 | CATTCTACACAGTCA[C/T]TGAGACCAAAAATAA | 23077 |
rs7325581 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77271798 | aattgcccagtctcg[G/T]gtacatctctatcag | 23077 |
rs7325942 | snp | C/T | 0.448708 | 0.151707 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183585 | tgagatggagtatca[C/T]tctgtcaccaggctg | 23077 |
rs7326047 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77317798 | aaaaattagctgggc[A/G]tggtgatgtgcacct | 23077 |
rs7326637 | snp | A/C | 0.00563376 | 0.0527744 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77060758 | TAAATATCATAAAAT[A/C]ATACAACCTTATAAT | 23077 |
rs7327067 | snp | G/T | 0.0670745 | 0.170406 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77193160 | aaatgaataaataaa[G/T]aaataaataaataCG | 23077 |
rs7328012 | snp | C/G | 0.405776 | 0.195535 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77275543 | AGACTCTCAGAAGGA[C/G]ctgggtgcagcagtg | 23077 |
rs7330809 | snp | A/G | 0.197082 | 0.244335 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77126774 | AGCAGGAAACCAGTC[A/G]ACCTCTGGCTTCTGC | 23077 |
rs7330984 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77309811 | TAACTCTACCATTAC[A/G]TTGCTTAAAAACCTA | 23077 |
rs7331598 | snp | A/G | 0.167158 | 0.235875 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77280018 | TCCCATGCCTAGCCA[A/G]TTACCTAGCATATGG | 23077 |
rs7333898 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77273089 | AATATATCAGATTGA[C/T]ACCATATCTTTTTCT | 23077 |
rs7334244 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77179977 | GAGAAAGTAGGAGGT[A/G]GAGAGAAAGGCAAAA | 23077 |
rs7334479 | snp | A/T | 0.487113 | 0.0792303 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267424 | AAAATTAAATTAAAT[A/T]AAATAAAATTAAATT | 23077 |
rs7336511 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77324561 | TAAACAATAATGTTG[C/T]GTTGAACAAGCATTA | 23077 |
rs7337555 | snp | A/G | 0.124491 | 0.216211 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77294813 | TTTTTCTGCCTACCC[A/G]GCAACACTTTCCTTA | 23077 |
rs7337686 | snp | A/G | 0.449345 | 0.150869 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77149275 | CTACCTTGTAAATCA[A/G]TATTTCTCAAAGTTT | 23077 |
rs7338017 | snp | G/T | 0.0648419 | 0.167978 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237304 | gcaaatgtatataca[G/T]aatactacttttgtA | 23077 |
rs7338027 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237331 | tgtAAATAAACATAT[C/G]TCTACACTTTCACAT | 23077 |
rs7339290 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77310863 | GGGAAAATCTTTTTT[A/T]AAAGCCAGATAAGag | 23077 |
rs7339360 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210487 | gtgagccaccgcacc[C/T]ggccCAGCACCACAA | 23077 |
rs7350694 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77115358 | CTAAAAACTATATAA[C/T]TAGTTTTTAAATTAA | 23077 |
rs7981256 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77219569 | AGAAATAGATCTCTA[A/C]GGAAAAGACAGCTAG | 23077 |
rs7981372 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260200 | CACAGCTACAGCGAA[G/T]CTTCCCTTGCCAAGC | 23077 |
rs7981603 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77274228 | TGAAATTGAGATATG[G/T]GGTATCAAAAGATTT | 23077 |
rs7982178 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77321510 | ATCAAGGGTGATCAG[C/T]GTCTACTGAATAAAA | 23077 |
rs7983622 | snp | C/G | 0.15665 | 0.231917 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77198935 | TAGTCTTTCTTCAGT[C/G]GTAAATTGTTGAAAA | 23077 |
rs7984798 | snp | C/T | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77229112 | CTGGAACTTAAGAAC[C/T]TGGACTGGAATCTTG | 23077 |
rs7984926 | snp | C/T | 0.449345 | 0.150869 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77153315 | gctggagcccagagg[C/T]gcttgcctgggccct | 23077 |
rs7984991 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77156592 | ATCCTGCAAGCCTGG[A/T]AAAAGCAGTGTCTCT | 23077 |
rs7985293 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77104264 | TTTTCGGCTGATTCA[C/T]TATTATGATCAAGAT | 23077 |
rs7985513 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77113364 | TTCTTTAACTAGGTT[A/G]TATCTCTTAAAATAT | 23077 |
rs7985922 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77162306 | TGGGCCTTTATATTT[C/T]GGTTGCCTTACAGAA | 23077 |
rs7986413 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77157165 | atcacagcaacctcc[A/G]cctctagggtttgag | 23077 |
rs7987716 | snp | A/T | 0.0729998 | 0.176553 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77147341 | TTTCTTAATAAAAAA[A/T]TAACAAAATGACCTG | 23077 |
rs7988781 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056803 | GTTTTAAATGGACAA[C/T]TACTGTTTTGAGATG | 23077 |
rs7988932 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77134489 | cagtgagccaagatc[A/G]tgccactgaactcca | 23077 |
rs7989377 | snp | A/G | 0.453453 | 0.145282 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77150443 | CACTGTTCCTGGTCA[A/G]AAGTAGACAAGTACT | 23077 |
rs7990717 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77171776 | ATGCAACTATACAAT[A/T]ATAGGGAATGATAAG | 23077 |
rs7991008 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050432 | GGTATTCCACCTCAC[C/T]GTTGCCACTAGCCTC | 23077 |
rs7991286 | snp | A/G | 0.198324 | 0.244601 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77108373 | AAAAATTCTGAGCAT[A/G]ATTTGATGGGTATAT | 23077 |
rs7991760 | snp | C/T | 0.493154 | 0.0581045 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050837 | TGCTTCCTAATTCAC[C/T]CAGAAAGTCATAAGC | 23077 |
rs7992704 | snp | C/T | 0.49334 | 0.057322 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77087393 | TTCAAGTTAGATCTG[C/T]GAATGATTTCATGCA | 23077 |
rs7992812 | snp | C/T | | | splice-acceptor-variant | MYCBP2 | GRCh38.p7 | 13:77205384 | AGCCTCCTCCATGAC[C/T]TAGAATATATAAATC | 23077 |
rs7995002 | snp | C/T | 0.406123 | 0.195258 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77175701 | CGCGGTGGCTCACGC[C/T]TGTAATCCCAGAACT | 23077 |
rs7995223 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77193396 | GTATCTTACGATCAT[C/T]CTTGTTTCTGAAAAT | 23077 |
rs7995708 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77279607 | GAAGTAACAGAAAAA[C/T]TGAAATAAGACTAAT | 23077 |
rs7995762 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251551 | CCATTTCATTTCTGC[A/G]AAAGAAGGCAAGGAA | 23077 |
rs7996439 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77201165 | ctcacgtgcagagac[A/G]catataggctcaaaa | 23077 |
rs7996862 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77155032 | CTATTCCATCATATA[C/T]TATATTTATATCTTT | 23077 |
rs7997138 | snp | C/T | 0.00493995 | 0.0494527 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77144417 | GTTATTTGAAGTAAG[C/T]AGTAGCTCATGGCTT | 23077 |
rs7997330 | snp | C/T | 0.102726 | 0.202016 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77328150 | ATATCTGTGCCTCTT[C/T]TTCGGATGGCCTTCT | 23077 |
rs7997481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77201168 | acgtgcagagacgca[C/T]ataggctcaaaataa | 23077 |
rs7997490 | snp | A/C | 0.0256215 | 0.110247 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77328201 | atgttaaaaaatCCT[A/C]CTTAGTGTTTGAGAA | 23077 |
rs7998168 | snp | C/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130546 | ATGCCTACAAATAAA[C/T]GTAAACCAAAACCAA | 23077 |
rs7998514 | snp | C/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071205 | TATGTGCACGCTGTT[C/G]TTCTAAGTGCCACat | 23077 |
rs7999576 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77102956 | TAATGATCTCATAAA[A/G]TTTTAAAATTAAGTA | 23077 |
rs7999635 | snp | C/T | 0.0131093 | 0.0800529 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77103139 | CATGACTGAGACGAA[C/T]GGAAACATCTTTAAT | 23077 |
rs7999924 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77294740 | TTGACAATGCGCTCC[A/T]CTTCCCTCCTCTATC | 23077 |
rs8001055 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77215894 | cctatgatttctaaa[A/T]tacatacatatatgt | 23077 |
rs8001178 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77245836 | ataatacatatatat[A/G]tatatatatatgtat | 23077 |
rs8001793 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77280503 | ACTACTATATTCTGT[C/T]ATTCTTTCAGATTGC | 23077 |
rs8002400 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77282829 | CACACaaaaccttta[A/G]gaatatctttagatt | 23077 |
rs9318462 | snp | A/C | 0.496105 | 0.0439572 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77123379 | CTTTTCTTAAATGAT[A/C]CTCTAATTTAAGAGG | 23077 |
rs9318463 | snp | C/T | 0.494442 | 0.0524218 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77135179 | TTTCAGTACTTTCAC[C/T]TCTTTTTAAGTTAGC | 23077 |
rs9318464 | snp | C/G | 0.133777 | 0.221342 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77138198 | TTCCTTCTCTTTCTT[C/G]CTCTCTGTCTATATA | 23077 |
rs9318465 | snp | A/C | 0.157972 | 0.232445 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77162748 | TGCAACCTCCACCTC[A/C]TGGGTTTAAGTGATT | 23077 |
rs9318466 | snp | C/G | 0.452965 | 0.145963 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77164011 | TCTTATCTACTTGCT[C/G]TAGAATATCTTTCAT | 23077 |
rs9318467 | snp | A/T | 0.0188097 | 0.0951371 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77164432 | ACCCTATCAAAAAAC[A/T]TCCAGTATTGGCCAC | 23077 |
rs9318468 | snp | A/T | 0.448963 | 0.151372 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165156 | GTGAGCCACTGCACC[A/T]GGCCCCAATTTTTCG | 23077 |
rs9318469 | snp | A/T | 0.350982 | 0.228698 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210957 | TTGTGGAGCTGGGAT[A/T]AACCTAGGTAGTGTT | 23077 |
rs9318470 | snp | A/T | 0.495596 | 0.0467178 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77254377 | AATCTTATCTGTGAT[A/T]TTTTTTTAACTGAAA | 23077 |
rs9318471 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77262561 | GGAGAGGTTAGTCCA[C/G]ACACAGAGTCATTCA | 23077 |
rs9318472 | snp | A/T | 0.108755 | 0.206276 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267434 | TAAATTAAATAAAAT[A/T]AAATTAAATTAAATA | 23077 |
rs9318473 | snp | C/G | 0.494855 | 0.0504572 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77299398 | CAGGCCATCCAAGAA[C/G]TAGCTATTCCCAAAT | 23077 |
rs9530620 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77068897 | ACTACTCCTAGCAAA[A/C]CAAGCAAACAAAAGA | 23077 |
rs9530621 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77108939 | acctcgtgattcacc[C/T]gcctcatcctcccaa | 23077 |
rs9530622 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77133342 | ATATGTTAGAAATTA[C/T]TTTAAACAGAATGAT | 23077 |
rs9530623 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160302 | TTGCTCACTAGCTGT[A/G]TGATCGTGGGCGAAC | 23077 |
rs9530624 | snp | C/T | 0.348574 | 0.229746 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169179 | TTTGGGAGGGCGAGG[C/T]GGGCGGATCACGAGG | 23077 |
rs9530625 | snp | G/T | 0.495596 | 0.0467178 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77214302 | ttcaacacagtaatc[G/T]cacttctaggaattt | 23077 |
rs9530626 | snp | C/T | 0.347253 | 0.230308 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77229469 | ACCAAATGGTTGAAA[C/T]CTTAAATCCTTTGTA | 23077 |
rs9530627 | snp | C/T | 0.420255 | 0.183066 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77244292 | TAGGATTAAGTGACC[C/T]AGATGGGTTGGTTGG | 23077 |
rs9530630 | snp | C/G | 0.495671 | 0.0463237 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77281924 | GAAAAAGCTCAAAAG[C/G]AAATCAAAATTATAT | 23077 |
rs9530631 | snp | A/G | 0.445724 | 0.155538 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77288849 | ACTTAATTTTCATCA[A/G]CTCATTTCATTCTCA | 23077 |
rs9530632 | snp | C/T | 0.499885 | 0.00758699 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77292696 | aggcacggtggcttg[C/T]gcctgtaatcccagc | 23077 |
rs9530633 | snp | C/G | 0.495708 | 0.0461266 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77299139 | GCATCAAAATTTATT[C/G]CAAACCAATTTTCAG | 23077 |
rs9530634 | snp | A/G | 0.421209 | 0.182174 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303061 | attaatcggccaggc[A/G]cggtggctcatgcct | 23077 |
rs9530635 | snp | C/T | 0.358303 | 0.225323 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77317096 | CTGGGATTACAAGCA[C/T]GCGCCAACATGCCCG | 23077 |
rs9530636 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77317219 | ggcctcccaaagtgc[C/T]gggattacaggcgtg | 23077 |
rs9544415 | snp | A/G | 0.491473 | 0.0647364 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77054747 | CTGGGACTACAGGCA[A/G]ATGCCAACCTACCTG | 23077 |
rs9544416 | snp | A/G | 0.304438 | 0.244001 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77089611 | CCCAGCTCCAATTTG[A/G]GGCTGTTGATACCAA | 23077 |
rs9544417 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77090298 | ACAGATACAAACTCA[A/G]AAGAGCTGAATGAAA | 23077 |
rs9544419 | snp | A/C | 0.35574 | 0.226537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77112173 | attttacttagaaaa[A/C]agaGCTCCCAATAAT | 23077 |
rs9544420 | snp | C/T | 0.432797 | 0.170544 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77113298 | TTTCCTATGTTTCCA[C/T]TGCATCCTGTGACTA | 23077 |
rs9544421 | snp | C/T | 0.489201 | 0.0726845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118665 | CCTCAGATTAGGGAC[C/T]GAATTTTGCAAGCTT | 23077 |
rs9544422 | snp | A/G | 0.418974 | 0.184249 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77139821 | TCTGAATACTATGTC[A/G]AACATTGTTCTTTTC | 23077 |
rs9544424 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77141859 | attATTATAACTATT[A/C]TAGTGAATTATTATC | 23077 |
rs9544425 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77141884 | ATTATCTCTGCTTGT[A/C]TATGGTCAAGCAAGG | 23077 |
rs9544428 | snp | C/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77173660 | TAATGCCAAGTCAGG[C/T]TGAGGACAAATGTGG | 23077 |
rs9544431 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183687 | ctcccgagtagctga[A/G]attacagctgtgcac | 23077 |
rs9544432 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183874 | cacttttgattatgg[G/T]atttcatgttttttc | 23077 |
rs9544433 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77189553 | AAAGATAGGGAGATA[A/G]AATCACAGTTCTAGA | 23077 |
rs9544434 | snp | A/G | 0.433818 | 0.169443 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77193289 | CTAAAAAAATCTTGC[A/G]ATATTAGTTAATGCC | 23077 |
rs9544435 | snp | A/C | 0.494484 | 0.0522255 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77201378 | cccaatacaggagca[A/C]ccagattcataaagc | 23077 |
rs9544437 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77218921 | TGAAGGCCTTAACTA[A/G]GAGCAGTGCAGAGTG | 23077 |
rs9544438 | snp | A/C | 0.347032 | 0.230401 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243446 | GGTGAAACCCCGTCT[A/C]TACTAAAAATACAAA | 23077 |
rs9544439 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77246039 | ACAAAGACACTCCCA[A/G]AAACTGACTTGGGGT | 23077 |
rs9544440 | snp | C/G | 0.495252 | 0.0484902 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77248860 | caatgtggaagcaac[C/G]aaagtgttcatcagt | 23077 |
rs9544441 | snp | A/G | 0.432797 | 0.170544 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77258711 | AAAAGGTAAGGGTGT[A/G]TGTATATATATAAAA | 23077 |
rs9544442 | snp | G/T | 0.494143 | 0.0537956 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260113 | CATGAAAATCACTTC[G/T]TCAGGATACTACCAC | 23077 |
rs9544443 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77261661 | acaatagtaacatca[A/G]agataacagatcacc | 23077 |
rs9544446 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77275140 | TGACAAAGAATGTCT[C/T]TACCCTTTCAAAAAG | 23077 |
rs9544447 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77288132 | CTGCAGGTTACACAT[C/T]TAAATATTAATAGAA | 23077 |
rs9544449 | snp | A/C | 0.495708 | 0.0461266 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77293993 | ATAAGAGTTTTTCTA[A/C]AAAGAAAGACTGGTA | 23077 |
rs9544450 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294131 | ATATATATATATATA[C/T]ATATATATATACATA | 23077 |
rs9544451 | snp | A/C | 0.495745 | 0.0459295 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77297831 | ATCTCATAAACAGTT[A/C]TTGAATCTGTCCACA | 23077 |
rs9544452 | snp | C/T | 0.449345 | 0.150869 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300917 | CTTCCATGGGGGTAA[C/T]TGCAGAGCTTGGGCA | 23077 |
rs9544453 | snp | C/T | 0.495521 | 0.0471118 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300993 | GAAACAAGAGACTAG[C/T]AGTGCTTTAGATGCC | 23077 |
rs9544454 | snp | C/T | 0.421368 | 0.182025 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77301377 | GCCAAGAGCCAAGAT[C/T]GCGCCACTGCACTCC | 23077 |
rs9544455 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77301418 | acagagcaagactcc[A/T]tctcaaaaaaaaaaa | 23077 |
rs9544456 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77301448 | AAAAAAAAAAAAAAA[A/C]AGAGGCTGGGTCAAA | 23077 |
rs9544457 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303700 | ttgacataacaaaat[C/T]ggtagaatgctgcta | 23077 |
rs9565316 | snp | A/C | 0.185472 | 0.241529 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080014 | TGAGGGAGAGTATGT[A/C]CTTGCTTAAAATGTA | 23077 |
rs9565318 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77094690 | TCGCTTTCTTCCTGT[C/T]GCTTGCCTGACAGAT | 23077 |
rs9565319 | snp | C/T | 0.124837 | 0.216412 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77112199 | ATAATATACATACTT[C/T]TTTCTTGCTTGTTAT | 23077 |
rs9565320 | snp | C/T | 0.126219 | 0.217206 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130430 | ATATGGATATATACA[C/T]ATATATGTACAGATG | 23077 |
rs9565321 | snp | C/T | 0.125528 | 0.21681 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77149958 | ATATTCCACCACAAT[C/T]GTTACAAAACACAAA | 23077 |
rs9565322 | snp | G/T | 0.179425 | 0.239831 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77157418 | TTGTAGACACAGGAT[G/T]TCACCATGTTGGCCA | 23077 |
rs9565323 | snp | C/T | 0.125874 | 0.217008 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77163271 | AAATTTAACAGCTAT[C/T]GACAAAAATAGGTTG | 23077 |
rs9565324 | snp | A/C | 0.168135 | 0.236216 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77205063 | taataataaataaaT[A/C]AATTTAAAAAATTTA | 23077 |
rs9565325 | snp | A/C | 0.49655 | 0.04139 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210353 | GCCCGCCACCACGCC[A/C]GGCTAATTTTTCGTA | 23077 |
rs9565326 | snp | C/T | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77227487 | ACACACACATACACA[C/T]ACACACACACACACA | 23077 |
rs9565327 | snp | C/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77230194 | TCTCCAACTTTCCAT[C/G]TTAGAACTTAGTCCT | 23077 |
rs9565328 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77233542 | AATAGTCTCAAATAG[A/G]TAATCAAGAAGTTCA | 23077 |
rs9565329 | snp | A/T | 0.475525 | 0.107882 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267409 | AAAATAAAATAAAAT[A/T]AAATTAAATTAAATT | 23077 |
rs9565330 | snp | C/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77268382 | TCCACGGCATTATTT[C/T]TTAGATAAAACACAA | 23077 |
rs9565331 | snp | C/G | 0.122411 | 0.214991 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285810 | AAGGAAAGGGAAAGG[C/G]AAAGGAAAAGGGAAA | 23077 |
rs9565332 | snp | C/T | 0.167809 | 0.236103 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286953 | gcagtggcgccatct[C/T]ggctcactgcaagct | 23077 |
rs9565333 | snp | A/G | 0.114036 | 0.209795 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77290712 | ctaaggagagggtga[A/G]gaaggaagatacctg | 23077 |
rs9565334 | snp | C/T | 0.494651 | 0.0514399 | intron-variant, utr-variant-5-prime | MYCBP2 | GRCh38.p7 | 13:77290754 | gatatcacagagaat[C/T]cttgtgatggaactg | 23077 |
rs9565335 | snp | C/T | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294129 | ATATATATATATATA[C/T]ACATATATATATACA | 23077 |
rs9573991 | snp | A/C | 0.114252 | 0.210125 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77058434 | AATTACAATGTTACA[A/C]AAGTATGTAAAAAAG | 23077 |
rs9573992 | snp | C/T | 0 | 0 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77075620 | ATCTGCAATTTTTTT[C/T]ACACATTTAATAACT | 23077 |
rs9573993 | snp | A/G | 0.00477324 | 0.0486193 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77077678 | CGATATGGCTTCCGA[A/G]CAAAATTATATGAGT | 23077 |
rs9573994 | snp | A/G | 0.493793 | 0.055364 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77079670 | GAAATATTTGGGACT[A/G]GAAGTGTTTTGGATT | 23077 |
rs9573995 | snp | C/T | 0.126219 | 0.217206 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77083263 | CACAAAAGACTATTA[C/T]GTATACTTAAAAAAT | 23077 |
rs9573996 | snp | A/G | 0.434976 | 0.168179 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77113628 | AATGCACTGGGACAA[A/G]ATGTCTTGTAAGCAA | 23077 |
rs9573997 | snp | A/T | 0.494692 | 0.0512434 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77115295 | AGATACAGATATCAT[A/T]CTCCACTTTGGTTCA | 23077 |
rs9573998 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77121139 | TTTTAAATAGAAAAA[A/T]AATAAGCAAGCACTC | 23077 |
rs9573999 | snp | C/T | 0.123105 | 0.215401 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77122121 | TGGCAAATGTTTTAT[C/T]CATTTACAAATGGCA | 23077 |
rs9574000 | snp | C/T | 0.179744 | 0.239925 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124669 | TTCACTATGACACTA[C/T]TGTTCTAGTGGTGAG | 23077 |
rs9574001 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124928 | ATTTATTCAATGCTC[C/T]TTCCCTAAGACAAAA | 23077 |
rs9574002 | snp | C/T | 0.0140344 | 0.0825847 | missense, intron-variant | MYCBP2 | GRCh38.p7 | 13:77126326 | TCCATACCTCTCCCA[C/T]TGCTTTGACTTTGTT | 23077 |
rs9574004 | snp | C/T | 0.178465 | 0.239547 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131728 | ACGAACACACATATA[C/T]ATAAAATAACATTTC | 23077 |
rs9574005 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77132459 | TCAAATCTTTCAGGT[C/T]CCAAAATTTGGAAAA | 23077 |
rs9574006 | snp | A/C | 0.470718 | 0.117404 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77150971 | ATGGTATTATAGAAA[A/C]CAAATACCATTATTA | 23077 |
rs9574007 | snp | A/C | 0.318415 | 0.240457 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77167025 | CACACACACACACAC[A/C]CCAAATGAAATAATT | 23077 |
rs9574008 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174919 | TATATATAATATATA[A/T]TATATATATATAATA | 23077 |
rs9574009 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174953 | atatattttatatat[A/T]atatatatatatttt | 23077 |
rs9574010 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174954 | tatattttatatatt[A/T]tatatatatattttt | 23077 |
rs9574011 | snp | A/C | 0.031825 | 0.122064 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77187734 | TGATACGTACTAATA[A/C]GTTTTTTTGCATATA | 23077 |
rs9574012 | snp | C/G | 0.267091 | 0.249415 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77196585 | acgataatatttgct[C/G]ccgaagtggatgtgt | 23077 |
rs9574013 | snp | C/T | 0.166506 | 0.235645 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77198319 | CTTTTTTAGCATGTA[C/T]TCCAACTATAACCAG | 23077 |
rs9574015 | snp | C/T | 0.125874 | 0.217008 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77216397 | tcaatggatgctaaa[C/T]ctagggggaaatttt | 23077 |
rs9574016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77217680 | AAAGAATATCATTCA[A/G]GTTTAGTGTGTGTTG | 23077 |
rs9574017 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77220019 | ACCATTGTACAGGAA[C/T]TGGTTGAATCTGGAA | 23077 |
rs9574018 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77227481 | ACACACACACACACA[C/T]ACACACACACACACA | 23077 |
rs9574019 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237936 | AAACCATAATGGTTT[G/T]AAGGGCTTAAAAAGT | 23077 |
rs9574020 | snp | A/C | 0.125874 | 0.217008 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238010 | GCACTTTGGGAGGCC[A/C]AGGCAGGCGGATTAC | 23077 |
rs9574021 | snp | A/G | 0.125874 | 0.217008 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77239199 | ATAAGATGAGACAGA[A/G]AAGTCAAGTAAAATA | 23077 |
rs9574022 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77246192 | GTACAAAAGGAAGAA[C/T]ATATCTGGCAGCAGT | 23077 |
rs9574023 | snp | C/T | 0.495818 | 0.0455352 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77250746 | TTTAAAACAAAACTA[C/T]ATATCTAATCAAGTA | 23077 |
rs9574024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77258925 | GTAAACTGTTACCCA[A/G]TTAAAGATTAAGTAA | 23077 |
rs9574025 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77284256 | AAAAAAAAAGAGTAC[A/G]AGAAACAGAAACCTC | 23077 |
rs9574026 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77284260 | AAAAAGAGTACAAGA[A/G]ACAGAAACCTCAGGC | 23077 |
rs9574027 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77284348 | AGCAAACTAGGATAA[C/T]AGCAGCATTTGGGGC | 23077 |
rs9574028 | snp | C/G | 0.495445 | 0.0475058 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77284378 | CTGAGGCACAGAGAA[C/G]GTCAAAGGGAAAAGA | 23077 |
rs9574029 | snp | A/G | 0.495596 | 0.0467178 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77287063 | ctaagttttttttgt[A/G]tttttagtacagacg | 23077 |
rs9574031 | snp | C/T | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294135 | atatatatatacata[C/T]atatatacatatata | 23077 |
rs9574032 | snp | C/T | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294143 | atacatatatatata[C/T]atatatataaaatat | 23077 |
rs9574033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77302820 | aaaagaaatgaaaag[A/G]gcatttctaaatggc | 23077 |
rs9574034 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303247 | ctgaggcaggagaat[C/T]gcttgaacccgagag | 23077 |
rs9574035 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307459 | agcaagaccccgtct[C/T]tattaaaaaaaaaaa | 23077 |
rs9574036 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307852 | TCCCGCCAgcttcta[A/G]aacctctactttagt | 23077 |
rs9593209 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77127802 | ATTCAAGAATTCTGT[A/C]TACCTGCTACTTTGT | 23077 |
rs9593210 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77149426 | ccagatgcttctgat[A/G]tagagaagagtctga | 23077 |
rs9593211 | snp | C/G | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77161199 | ATTTCCATCCTATTA[C/G]AGATTACTAGCTAGC | 23077 |
rs9593213 | snp | G/T | 0.103082 | 0.202275 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169139 | ACAggccgggcgcgg[G/T]ggctcacgcctgtaa | 23077 |
rs9593214 | snp | C/T | 0.193653 | 0.243567 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77181588 | AAGCACCAAGCTAAA[C/T]ACGCTTAGCTTGGTG | 23077 |
rs9593215 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195524 | attgcttgaacccag[A/G]aggcagaggctgcag | 23077 |
rs9593216 | snp | A/C | 0.191775 | 0.243125 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77241332 | AGTAACAAGATACAC[A/C]GCATTAGGCAAGTAA | 23077 |
rs9593217 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77245834 | aaataatacatatat[A/G]tgtatatatatatgt | 23077 |
rs9593218 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77247302 | tcagttgtatttcta[A/G]acactaacaatgaac | 23077 |
rs9593219 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276031 | TACTTTCCTCCATAC[A/G]ATTTATCCACATTTG | 23077 |
rs9593220 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77279926 | TGTTGGGATCTTCCA[A/G]TATACAAGGAACATG | 23077 |
rs9593221 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77280109 | CATCTCAGAAATACA[C/T]TTTCTAAACCAGAAG | 23077 |
rs9593222 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285872 | GGGAAAGGAAAGGAA[A/G]GGAAAGGAAAGGAAA | 23077 |
rs9593223 | snp | C/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285899 | GAAAGGAAAGGAAAG[C/G]AAAGGAAAGCAAAGG | 23077 |
rs9593224 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307075 | agaaaatttaagatc[C/T]agaaaacagatcaga | 23077 |
rs9593225 | snp | A/G | 0.417034 | 0.18601 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77320671 | AATCTAGTAGGTACC[A/G]TCTTACCCAAGTAAT | 23077 |
rs9600809 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77049856 | ggccaggctggtctc[A/G]tactcctgacctcaa | 23077 |
rs9600810 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055842 | TTAGCATGCACCTAA[A/G]TGCCAAGCATTGTGC | 23077 |
rs9600811 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056451 | CTGCCACATTCTTCA[A/G]AAACAGCTTTTTGTT | 23077 |
rs9600812 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77058697 | CAGCTATAAAGCAAA[A/G]AGTTCCTggctggga | 23077 |
rs9600813 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072556 | aagaaataaagttgt[A/G]attattaaaagaagc | 23077 |
rs9600814 | snp | C/T | 0.205417 | 0.245993 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77073114 | cagcatttttattac[C/T]tctaaaagaagcact | 23077 |
rs9600815 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77107542 | aggagtttgagacca[A/G]cttaggcaacatggt | 23077 |
rs9600816 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77111205 | AATTTTCTATTTTCA[A/G]CTTGTCAGTCAACAA | 23077 |
rs9600817 | snp | C/T | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118995 | ATTAACATAGCAATG[C/T]GTTTACATTATAGTT | 23077 |
rs9600818 | snp | A/G | 0.108755 | 0.206276 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77122607 | aggcaggagaatggc[A/G]tgaacctgggaggcg | 23077 |
rs9600819 | snp | A/G | 0.466515 | 0.124985 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124668 | CTTCACTATGACACT[A/G]TTGTTCTAGTGGTGA | 23077 |
rs9600820 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77129328 | CAACATTTTTCTGTA[C/T]TCTAGCACCAACATG | 23077 |
rs9600821 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130148 | AGTGAGTAGCAATTG[C/T]ACAATTTTATTGCTT | 23077 |
rs9600822 | snp | C/T | 0.158302 | 0.232576 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77154586 | ACAACTAAAGAAATA[C/T]CAGAAGCGTAACAGT | 23077 |
rs9600823 | snp | A/T | 0.15665 | 0.231917 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77154958 | CATATTATGTATGTA[A/T]GTGTGTATGTATATA | 23077 |
rs9600824 | snp | A/G | 0.199873 | 0.244923 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77157416 | TTTTGTAGACACAGG[A/G]TTTCACCATGTTGGC | 23077 |
rs9600825 | snp | C/T | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77157499 | aaagtgctgggatta[C/T]aggcatgagccattg | 23077 |
rs9600826 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77167708 | TTGTATCAATAAATA[C/T]CATAAatgtgcttta | 23077 |
rs9600827 | snp | A/G | 0.101658 | 0.201233 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169191 | aggcgggcggatcac[A/G]aggtcaggagatcga | 23077 |
rs9600828 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169312 | gaggcaggagaatgg[C/T]gtgaacccggaaggc | 23077 |
rs9600829 | snp | C/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169350 | gcagtgagcggagat[C/G]gcgccacagcactcc | 23077 |
rs9600831 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77173770 | AAAAGATTTTTTTAA[C/G]CCAAGGGTTGTTATC | 23077 |
rs9600834 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77215001 | tatatatcttcacaa[A/G]aagaaacacaagaag | 23077 |
rs9600835 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77222375 | AACCTCTTGATAGTA[C/G]TATCAATTTTATGTT | 23077 |
rs9600836 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77222605 | TTTAGAAAAAACTCT[C/G]ATGCTGGCATCCTAT | 23077 |
rs9600837 | snp | A/C | 0.155325 | 0.23138 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77222934 | ATTCTGGCATATACA[A/C]TGTGACTGCGAGGAA | 23077 |
rs9600838 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77224705 | TTTAGTTCTGAAAAA[C/T]ATTTTTGTAGGTCAT | 23077 |
rs9600839 | snp | C/G | 0.158302 | 0.232576 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228176 | GGCCAAAAATTTAGT[C/G]CAAATTCAAGAACCA | 23077 |
rs9600840 | snp | C/T | 0.133435 | 0.221162 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238727 | GCAGTAATATCATTG[C/T]TTTCTTGGGTTTCAA | 23077 |
rs9600841 | snp | G/T | 0.193028 | 0.243422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77239673 | TCCCCCAGTTTTTTG[G/T]TTCAGTAGAGATCTG | 23077 |
rs9600842 | snp | A/G | 0.078151 | 0.181571 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77250124 | gctacttgggaggtc[A/G]aggcaggagaatggc | 23077 |
rs9600843 | snp | G/T | 0.078151 | 0.181571 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77253225 | AATAATCAAGGGAAT[G/T]AAAATTAAAAGAAAA | 23077 |
rs9600844 | snp | A/C/T | 0.106055 | 0.204857 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77256241 | TGGGAAGATAATATA[A/C/T]GCCAGAAAGATTGCT | 23077 |
rs9600845 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77256504 | AATAAGAAATTCAGT[G/T]GTTTTCCTAATTCAC | 23077 |
rs9600847 | snp | A/T | 0.192401 | 0.243274 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77259697 | TGGGACAATTACATA[A/T]ATTTCTAATCATAAA | 23077 |
rs9600848 | snp | C/T | 0.103438 | 0.202533 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77269234 | TAGCTGTCTACTGAG[C/T]AGGCCAAACACTGTT | 23077 |
rs9600849 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77269280 | AATCTAGACTAAAAT[C/G]AAAGAGTCTGTGGTA | 23077 |
rs9600850 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77277558 | AGTTAGGTTCATGCA[A/G]TTTGGTTCTCACAGG | 23077 |
rs9600851 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77288091 | GTATTTTAGCAATGC[A/G]TATATATGCATTATA | 23077 |
rs9600852 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77295283 | GGACTACAGGCACCC[A/G]CCACCACGCCCAGCT | 23077 |
rs9600853 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300200 | TAAAATGGTTTCAAT[C/T]TTTTGCTTAATTTCT | 23077 |
rs9600854 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300206 | GGTTTCAATCTTTTG[C/T]TTAATTTCTCTTAGT | 23077 |
rs9600855 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77301542 | TCCCTCACTGGATTG[A/T]GATAATCAAACTCCT | 23077 |
rs9600856 | snp | A/G | 0.192088 | 0.2432 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307095 | AACAGATCAGAAAAA[A/G]AATCTGGAATTCTTC | 23077 |
rs9600857 | snp | G/T | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77313896 | agatggcaaataagc[G/T]ttatgaaaagatgtt | 23077 |
rs9600858 | snp | C/T | 0.191461 | 0.24305 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77314151 | ccacaatcactgttt[C/T]tggtattaacccaaa | 23077 |
rs9600859 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315439 | aatcaaattcagcaa[C/T]acattccaaatatga | 23077 |
rs9600860 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316132 | ggagaatctagagat[C/T]agaaagaaagacaat | 23077 |
rs9600861 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77318626 | gagtgtggtgggaca[C/T]gcctgtaatcccaac | 23077 |
rs9600862 | snp | C/T | 0.498253 | 0.0295011 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77319476 | AATTAAGTTTTGGGT[C/T]GAAGCCTTAGATTTT | 23077 |
rs9600863 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77319569 | CCCAATTATCTTCCA[A/C]CTTGCATCATCTTTC | 23077 |
rs9600864 | snp | A/T | 0.0988009 | 0.199095 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77320784 | ATTCTTGCTAAAAAA[A/T]TTTCTAATGAACACC | 23077 |
rs9600865 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77321007 | TATATGAAGTGATGG[A/G]AACAGTCTATACTTG | 23077 |
rs9600866 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77322814 | CACATTCAGAACAGA[G/T]CATACATTCCTTCAT | 23077 |
rs9600867 | snp | C/T | 0.0678174 | 0.1712 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77327529 | CGATCTTATTTTATA[C/T]GGTTTTTGTCATTAG | 23077 |
rs9635012 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77154109 | AAAGTGCTCCTAAGA[A/C]TTCATATACTAATAG | 23077 |
rs9635013 | snp | A/T | 0.0782982 | 0.18171 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77206874 | TGTGGTTTTGTTTTT[A/T]AAAAAAATTCCTAAA | 23077 |
rs9788300 | snp | C/T | 0.34659 | 0.230587 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77239676 | CCCAGTTTTTTGTTT[C/T]AGTAGAGATCTGAAG | 23077 |
rs9788363 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165159 | agccactgcaccagg[C/T]cCCAATTTTTCGAAT | 23077 |
rs9989089 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77129901 | AATCAATTTTATCAA[A/C]AGACAGGCCTACTTT | 23077 |
rs10400634 | snp | A/G | 0.346368 | 0.23068 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77187075 | TCGGCCTCCAAAAGT[A/G]CTGGGATTATAGGCG | 23077 |
rs10467631 | snp | A/G | 0.15698 | 0.23205 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186937 | CCCCCTCAGCCTCCC[A/G]AGCAGCTGGGACTAC | 23077 |
rs10467632 | snp | C/T | 0.15698 | 0.23205 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77213691 | TGGTTATAAATAAGC[C/T]ACATTTAAATTCATA | 23077 |
rs10544105 | in-del | -/AGAG | 0.0678174 | 0.1712 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77305688 | TTTTTAAAAAAAGAG[-/AGAG]CCATTTACCTACAAA | 23077 |
rs10681121 | in-del | -/AT/ATATAT | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071250 | TGTATATATATATAT[-/AT/ATATAT]GCATGCACGTGTGTG | 23077 |
rs10871102 | snp | C/T | 0.102014 | 0.201495 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260753 | CATGTCATTTAAAAT[C/T]AGTGAACCTGCTAGC | 23077 |
rs11149060 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77089223 | tctctgaaagtcata[C/T]agctattaagttgta | 23077 |
rs11149063 | snp | C/T | 0.193028 | 0.243422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77261998 | AATCAACAGATTGTA[C/T]TTTAATCTCTTAAAT | 23077 |
rs11330230 | in-del | -/A | 0.0107246 | 0.0724382 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77328169 | GGATGGCCTTCTCTT[-/A]AAAAAAAATAAAATA | 23077 |
rs11338423 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77301449 | AAAAAAAAAAAAAAA[-/A]GAGGCTGGGTCAAAA | 23077 |
rs11346823 | in-del | -/A | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055145 | GTTAAAAAAAAAAAA[-/A]GAAGAAGTAGTTAAA | 23077 |
rs11356712 | in-del | -/A | 0.0479149 | 0.147179 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77225762 | CTTCCATTTGCAAAT[-/A]TCACTAAATTAATAA | 23077 |
rs11419165 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77057856 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 23077 |
rs11423040 | in-del | -/G | 0.166506 | 0.235645 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77214701 | AACCTAGACGGTATA[-/G]TCTACTACATACTTA | 23077 |
rs11424523 | in-del | -/A | 0.5 | 0 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080950 | GAAAAAAAAAAAAAA[-/A]GCTGATTACACTATA | 23077 |
rs11436373 | in-del | -/A/AA/AAA | 0.503969 | 0.0818118 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77261385 | TATTAAAAAAAAAAA[-/A/AA/AAA]GGAATTATGGTACTT | 23077 |
rs11445912 | in-del | -/T | 0.0256215 | 0.110247 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77327792 | TCATTTAATGGTTTA[-/T]TTTTTTTCTGCCCAA | 23077 |
rs11617095 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169813 | TCTGCTCTTTTGAGC[A/G]AAACTATAGTTGACA | 23077 |
rs11617489 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77297305 | TCATTTCACTTAATA[C/T]GTTTTATGTTCACCA | 23077 |
rs11618512 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169966 | atggcacatagggtt[C/T]aagtatcttacccaa | 23077 |
rs11618643 | snp | C/T | 0.497907 | 0.0322805 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77139859 | AAATATAATTTTAGT[C/T]ATTTTTTAATGATAA | 23077 |
rs11839714 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300620 | GAAAGGAAAAAAATG[C/T]TTTATAGCTATGAGT | 23077 |
rs11839950 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195357 | atcctagcactttgg[C/G]aggctgaggcaggca | 23077 |
rs11841781 | snp | A/G | 0.0528381 | 0.153711 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77292974 | aaaaaaaaaaaaaaa[A/G]aaagaaagaaaaaaa | 23077 |
rs11842224 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316867 | TGTGTGCCAAACCTC[C/T]ATGCTCCACTGTGGA | 23077 |
rs11842331 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77099061 | ATAAAATTATAACTT[A/C]CTGATAATTTAGCCA | 23077 |
rs11842917 | snp | A/T | 0.34659 | 0.230587 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77175979 | ATAATAATAATAATT[A/T]AAAAAAAATAAAGAA | 23077 |
rs12017346 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77246684 | AGGcaaaaaaaaaaa[A/C]ccctacagaccaata | 23077 |
rs12017919 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77204190 | acaatgaactcaaac[A/C]aatttacaagaaaaa | 23077 |
rs12020468 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77203866 | agctgaaactggatc[C/T]cttccttacacctta | 23077 |
rs12100065 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77122562 | ggcgtggtggccggc[A/G]cctgtagtcccagct | 23077 |
rs12184642 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165170 | caggccCCAATTTTT[C/T]GAATAGAGGCAACAG | 23077 |
rs12184865 | snp | C/G | 0.191461 | 0.24305 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77319225 | gtgatagtcagtagg[C/G]gagagaggaggAGCT | 23077 |
rs12184883 | snp | A/G | 0.103438 | 0.202533 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77254136 | aatttgtagaaaaat[A/G]taaataacagattaa | 23077 |
rs12322978 | snp | C/T | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77142149 | AGAAAATTTTCACAA[C/T]GTCATTCTTGGCTAT | 23077 |
rs12427928 | snp | A/G | 0.125182 | 0.216612 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77198670 | GGCCCTTTTGGATAC[A/G]AATAGGTGTGGTAAC | 23077 |
rs12428482 | snp | C/T | 0.178785 | 0.239642 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77200649 | gccagagagaaaggt[C/T]gggttaccctcaaag | 23077 |
rs12428510 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77200723 | acaagccagaagaga[A/G/T]tgggggccaatattc | 23077 |
rs12428894 | snp | C/T | 0.00961516 | 0.0686668 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77062809 | GATTTTGAAAATACA[C/T]AGATACTCAGTGGCA | 23077 |
rs12560645 | snp | A/G | 0.422473 | 0.180978 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77200323 | taaatgaagtgaagc[A/G]agaagggaagtttag | 23077 |
rs12560646 | snp | C/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77200542 | aggaaatacagagaa[C/T]gccacaaagatactc | 23077 |
rs12560687 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77246563 | gaggaggagcaggag[A/G]agaaggagaaggagg | 23077 |
rs12560694 | snp | A/G | 0.431916 | 0.171483 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77153230 | ACTGAGCTGTTTAAC[A/G]CTTAGCCATCCACAG | 23077 |
rs12561353 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77246482 | gaaagaagagaagaa[A/G]gaagaagaaggaaga | 23077 |
rs12583330 | snp | A/T | 0.495483 | 0.0473088 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77205023 | CTGCACATTGTGCAC[A/T]TGTACCCTAAAACTT | 23077 |
rs12583337 | snp | G/T | 0.00888871 | 0.0660708 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77289674 | aactcatcaacattg[G/T]actggatatcctatc | 23077 |
rs12584070 | snp | C/T | 0.346811 | 0.230494 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77201449 | attaataaagggaga[C/T]tttaacaccccactg | 23077 |
rs12584170 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307457 | atagcaagaccccgt[C/T]tctattaaaaaaaaa | 23077 |
rs12584929 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77240793 | TTTCTGTTAATTTTA[G/T]TGCCATGGAAAGCAA | 23077 |
rs12585051 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77068426 | AAAAGGGAGTAAAAT[A/C]CAGGCCCCAAACAAA | 23077 |
rs12585692 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307232 | CACTTCCTCTCATAC[A/C]CCAGATCCCATTTCA | 23077 |
rs12585693 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307251 | GATCCCATTTCATTC[A/C]CCATCCTTGAGATTT | 23077 |
rs12860226 | snp | C/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77295846 | TCAAATATTCCATAT[C/T]GCCTTTTCTTTTGCA | 23077 |
rs12860612 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77109009 | GGATAAGATACTTTT[A/C]AAGTACTATTTGGAG | 23077 |
rs12861330 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77079016 | TCCTTCCTGATTGAC[C/T]CCACCCCATCCCTCC | 23077 |
rs12861817 | snp | G/T | 0.182614 | 0.240747 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77327475 | GGTTAATTCAGAGTT[G/T]AAGGCAGAGAAAACC | 23077 |
rs12862076 | snp | C/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77109092 | TGTTAATTAGGGAAA[C/G]TAGGGAAACTGTTCC | 23077 |
rs12864253 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77109084 | GGAATACGTGTTAAT[A/T]AGGGAAAGTAGGGAA | 23077 |
rs12865959 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77201289 | caaagatcaaaagag[A/C]caaagaaggccatta | 23077 |
rs12867447 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210378 | ttcgtatttttagta[G/T]agacagggtttcact | 23077 |
rs12868318 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77175160 | tagcctcaaactccc[A/C]agctcaagtgatcct | 23077 |
rs12869227 | snp | A/T | 0.350982 | 0.228698 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77272001 | GTTGGGGATGTGGTG[A/T]TGTGGCAGGTCTGTA | 23077 |
rs12869534 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77177142 | GTTTCTTGAAAAATG[A/C]CAATATAAAAAAAAA | 23077 |
rs12869635 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286585 | ggtgaaaccccgtct[C/T]tactaaaaatacaaa | 23077 |
rs12869694 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286756 | gctagactccgtctc[A/C]aaaaaaaaaaaaaaa | 23077 |
rs12869799 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286788 | aaaaaaaaaaaaaAA[A/G]Aatatatatatatat | 23077 |
rs12872012 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77180891 | cacaactgcactgta[A/G]actgggtgacagaat | 23077 |
rs12873039 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77054676 | cacaaacacagctca[C/T]tgcagcctcaacccc | 23077 |
rs12873963 | snp | C/G | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294169 | aatatatataaagta[C/G]atataAAGTAGATAA | 23077 |
rs12873969 | snp | G/T | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294180 | AGTAGATATAAAGTA[G/T]ATAAAATGCCAGCTA | 23077 |
rs12874100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169133 | AAGCCAACAggccgg[C/G]cgcggtggctcacgc | 23077 |
rs12874549 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238267 | aaaaaaaaaaaaaaa[A/G]gaaaTATGCCTGGAC | 23077 |
rs12874696 | snp | A/G | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77178243 | TATCAGTCATAATGT[A/G]TGAATAAATCATCAG | 23077 |
rs12875012 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169215 | agatcgagaccacgg[C/T]gaaaccccgtctcta | 23077 |
rs12875189 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77194262 | AAGGAAAGGAGAAAG[A/C]CAATCATTTATATAA | 23077 |
rs12877357 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77182425 | ATACTTACAAAATTT[C/T]ATAAAAAAGCATTAA | 23077 |
rs13343225 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77216143 | catgtcacaagaata[C/T]aggagccaacttgaa | 23077 |
rs13378900 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130991 | GTACAATGATATTTT[A/C]AAATGATGTTAACTG | 23077 |
rs17067178 | snp | C/T | 0.0175359 | 0.0919806 | synonymous-codon, intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77077154 | GACACTCACTTGAGA[C/T]GTAATCAGTCTGAAT | 23077 |
rs17067203 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77094918 | CATAGAAGCCAGGAT[C/T]TTGTTATATTCATAC | 23077 |
rs17067205 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77095290 | CAAATACCGAACTAC[C/T]CTAGATATCAATAAA | 23077 |
rs17067209 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77111647 | CAGACTGGTCCTAAG[A/C]ATTTTACTGCCTAAA | 23077 |
rs17067210 | snp | C/T | 0.110167 | 0.207236 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77111898 | AGTCTAAACTAAGTA[C/T]GGCTTACAAGACCCT | 23077 |
rs17067213 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77111958 | AAGACACTGACACTA[A/G]GTCACTTAAAGCTGC | 23077 |
rs17067242 | snp | A/C | 0.353154 | 0.227726 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77138704 | TCAACTAGAATACAA[A/C]GGAGCACCACAAATC | 23077 |
rs17067276 | snp | G/T | 0.00280453 | 0.0373417 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77165266 | TGAAAAGATAATTCA[G/T]TCTTACCTCATCAGG | 23077 |
rs17067287 | snp | A/C/G | 0.0175415 | 0.091996 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77171538 | CTTAGAGGCTCGAAC[A/C/G]ACAGTGCTTACAACA | 23077 |
rs17067297 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77194442 | CAAGGTTTTATGGTC[C/T]ACATTAATCTCTGTT | 23077 |
rs17067304 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77209964 | GAGAATGCAAGCAGG[C/T]ATGGGTAGAAGAAGG | 23077 |
rs17067313 | snp | A/G | 0.179744 | 0.239925 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77219505 | GAAGTTTAAAAGGTG[A/G]CTCAAAATAAAGACG | 23077 |
rs17067316 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77220008 | GAGGATTAATGACCA[C/T]TGTACAGGAACTGGT | 23077 |
rs17067321 | snp | G/T | 0.156319 | 0.231784 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77227393 | TCACTCCATCCAAAA[G/T]AAAATATACTCAGTT | 23077 |
rs17067328 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77229864 | AAAATAGACTCAGAT[G/T]TTTATCAGTGTGCCT | 23077 |
rs17067330 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77232616 | GTCTTCATGATTCGT[A/G]CTTTGCTTGCACTTA | 23077 |
rs17067332 | snp | C/T | 0.192088 | 0.2432 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77234464 | GTACCCTTCATTAAA[C/T]GTACAAGTGGGTAAA | 23077 |
rs17067337 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77236262 | CTTTCATTGGGAGAG[A/G]AGTGAGTAAAATAGG | 23077 |
rs17067338 | snp | A/T | 0.0869089 | 0.189476 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238686 | CACAAAGATTTAAAA[A/T]TAAAAAGTTCCAAAT | 23077 |
rs17067341 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238833 | AGCAAGGCTTTAGTA[A/C]AAGAACTAGGGCCCA | 23077 |
rs17067361 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77250919 | TTTTAAATAATGGTT[G/T]AAATGAATCAAATGA | 23077 |
rs17067377 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266935 | TGTAGTAAGGTTCAA[A/C]TAAATGTTTGATGAA | 23077 |
rs17067389 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77273400 | AAAAGCAGAATTCCT[A/T]TTGACAGAAATTGAG | 23077 |
rs17067419 | snp | C/T | 0.0139853 | 0.0824443 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77296981 | TTTATACTTTATCCA[C/T]AGTGGGATGTTTACA | 23077 |
rs17067421 | snp | A/G | 0.124144 | 0.21601 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77297590 | AAAAATTTTAAGCCT[A/G]GGTCACTTGGAGGTA | 23077 |
rs17067434 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307972 | TATATCACTTCTAAT[A/G]TGAGCTATCTGCTCA | 23077 |
rs17067437 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316825 | ACACTGGACAAGGAA[A/G]TACCAAGAGACACCT | 23077 |
rs17067442 | snp | C/T | 0.16618 | 0.23553 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77318014 | AACATAACAGTGGGT[C/T]CCTTATTCTGAAATG | 23077 |
rs17067468 | snp | C/T | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77325177 | TCTCCAACAGATAAG[C/T]CATGATACCTAGTGA | 23077 |
rs17327190 | snp | A/T | 0.0700422 | 0.173537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77129813 | ATTTGGAAATGTTTC[A/T]GAATGCTACTAACAA | 23077 |
rs17691989 | snp | C/T | 0.0258057 | 0.110621 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77093116 | CTAGTTCAAAGTCTT[C/T]CTTCCACCAAACACT | 23077 |
rs17692643 | snp | G/T | 0.084728 | 0.187577 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77141067 | ATCTGATTTCTGTCC[G/T]TTTAAGGTGATGGAT | 23077 |
rs17693263 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195219 | ACAGTCATTGGATTC[C/T]CTTTGTCCTACTAGT | 23077 |
rs17693337 | snp | C/T | 0.129664 | 0.219133 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77206530 | AGAGGATTTAACTTA[C/T]TTTGTACATTATTAT | 23077 |
rs17694524 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77298248 | TGAAATTCTCTACCA[C/T]GTCTTCTCCTGCTAA | 23077 |
rs17748954 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124559 | TGAGCAACTAGTATG[A/T]GTCAAAACTGTTTCA | 23077 |
rs17749801 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186222 | GCCCAAGACACTTTT[A/G]TAGTTCATTTATTAA | 23077 |
rs17750124 | snp | A/G | 0.195214 | 0.243923 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77220698 | ACATATGCTATAGAA[A/G]CTTTGTTCCTCCCAA | 23077 |
rs17750294 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77235119 | TGATTATCTTTTATT[C/T]AGCAGACACTAGGTG | 23077 |
rs17750691 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266827 | TTTTATTAAGTCATC[C/T]GCTTTCCAAAGCTCC | 23077 |
rs17762281 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316409 | TATTGCCAAAGGCAA[C/T]GCCCATATTGGAACT | 23077 |
rs28411709 | snp | G/T | 0.0286859 | 0.116276 | utr-variant-3-prime | MYCBP2 | GRCh38.p7 | 13:77044862 | TATGTTTATATACAG[G/T]GTGATACTTATTACA | 23077 |
rs28449300 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285856 | AAAAAGGAGAAAGGA[A/G]GGGAAAGGAAAGGAA | 23077 |
rs28457051 | snp | C/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286610 | TACAAAAAAAAATTA[C/G]CCGGGCGCGGTGGCA | 23077 |
rs28473347 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071239 | TATATATGTGTGTGT[A/G]TATATATATATGCAT | 23077 |
rs28478660 | snp | C/G/T | 1.65029e-05 | 0.00287248 | missense | MYCBP2 | GRCh38.p7 | 13:77059618 | CTGAGCTACTCGTGG[C/G/T]GGGTTTGCCTAGGTT | 23077 |
rs28488700 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77264814 | AGCAAAATCAACATC[A/G]AGGATAAATTCTGTC | 23077 |
rs28522795 | snp | A/G | 0.45235 | 0.146814 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77175103 | TCAGTTAATTTTTTA[A/G]GGTGTTTCTGTAGAG | 23077 |
rs28532764 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77224097 | ATATGTTTGAATCCA[C/T]TGCTGACATTTTTTA | 23077 |
rs28569186 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77318506 | CACGCCTGTAATCCC[A/C]GCACTTTGGGAGAAC | 23077 |
rs28582462 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77067350 | TCTAGAATTTTTTTT[A/T]ACATGGATATCCAAA | 23077 |
rs28627519 | snp | G/T | | | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77082443 | TTATCATTAGTAACA[G/T]GGGAAGCCCAAGCAT | 23077 |
rs28690917 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260135 | TACTACCACTGTCCC[A/G]GGGACATGTCCCATA | 23077 |
rs28722595 | snp | G/T | | | missense, intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77081926 | ACAAAATATTGTTAA[G/T]GTGATGAAAGACGTT | 23077 |
rs28758392 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77137632 | TTCGCTCTGTCTCCC[A/C]GGCTGGAGTGCAGTG | 23077 |
rs28868341 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77152947 | GCGGGTGCCTGTAGT[C/T]TCAGCTACTCGGGAG | 23077 |
rs33938909 | in-del | -/T | 0.451608 | 0.147832 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77111584 | TCAATGCTTGGCTAA[-/T]TTTTTTTTTTTTTCT | 23077 |
rs33953434 | in-del | -/AAG | 0.417034 | 0.18601 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055144 | GGTTAAAAAAAAAAA[-/AAG]AAGAAGTAGTTAAAG | 23077 |
rs33966568 | in-del | -/AA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77234845 | AAGGTAATAATATTG[-/AA]TTATATTACCATTTT | 23077 |
rs34000116 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77312710 | AAAGAGAAACAGAAG[A/C]CAATAAAGTGGCAGA | 23077 |
rs34009137 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77069795 | TGGTGTGAACCCAGG[-/A]AGGCGGAGCTTGCAG | 23077 |
rs34051925 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160065 | TTCAAAATCACAAAC[-/T]TTTTTTTTTTTTTTT | 23077 |
rs34059395 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77216114 | GAAAGGAAGCACTCC[-/A]AAAAATGAAGGGGCA | 23077 |
rs34077914 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77232196 | ATTTTTTTAAATTAG[-/A]ACTATGACAATTTTG | 23077 |
rs34090704 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77240723 | TCCTTTCGCATGATT[-/A]CTAGGTAACTGTGGT | 23077 |
rs34115628 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77168392 | GAACCTCATGCCAAG[-/T]TTTACATTCGAATCA | 23077 |
rs34124996 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77141788 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23077 |
rs34137754 | in-del | -/A/AA | 0.469148 | 0.120308 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77250222 | GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 23077 |
rs34172452 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77057232 | TAATGAAAATTCATT[-/G]GGGACACTGAAATTG | 23077 |
rs34173280 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77051749 | CCACCATATTATTGT[-/G]TTAAAAAATAATACT | 23077 |
rs34179471 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77138475 | AGTTTTTAAATAAAA[-/A]TTTTACCCGTGCTAT | 23077 |
rs34184406 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77193416 | TTCTGAAAATATACA[-/T]TTTTCACTAGCAAGA | 23077 |
rs34185499 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77163491 | GTAAAGATGGATTTT[-/G]GGGGGGGTAAGAAAA | 23077 |
rs34193418 | snp | C/T | 0.444444 | 0.157135 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77097232 | AAAACCCTGTACTGA[C/T]AATGTACTTTAAAAA | 23077 |
rs34199763 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77116396 | TGCTTGGGGAGTCTT[-/A]AAATGTTGGCACTTT | 23077 |
rs34201334 | in-del | -/C | 0.0182019 | 0.0936463 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77271505 | TGGTTTGGTTGTGTT[-/C]CCACTCAAATCTCAT | 23077 |
rs34203370 | in-del | -/G | | | frameshift-variant | MYCBP2 | GRCh38.p7 | 13:77061215 | ATTGTTTTAGAATCT[-/G]GCCAGTGCCATCAAC | 23077 |
rs34249338 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77189181 | GGTAATGCCAATACA[-/G]GGGCTTTTTTGAAAC | 23077 |
rs34275362 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77089246 | AGTTGTAGAGGTGGG[-/T]TTTTGAATCAGAGCT | 23077 |
rs34309468 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77146129 | AGCTGACAACACATG[-/T]TTTTGGTTATACTTT | 23077 |
rs34334283 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77179954 | GGTGAGAGAGAAGTA[A/C]CAAATCAGAGAAAGT | 23077 |
rs34343542 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77281348 | TTAATACCTCTTTAG[-/A]AAAATGTTCTGATTT | 23077 |
rs34356115 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323135 | TGTTAGTATTATGAT[-/C]CCCCATTCTACATAT | 23077 |
rs34371055 | in-del | -/C | 0.48546 | 0.0840147 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074003 | ATTCCATCCCCACCG[-/C]CCCCCCCCCTTTTTT | 23077 |
rs34380354 | in-del | -/A | 0.361684 | 0.223667 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072323 | AAAAAAAAAGAAATC[-/A]AAATGGGAATAAGAA | 23077 |
rs34383869 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77273891 | CTTATTTTTCTTAGT[-/A]AAAAAAGACAATCTA | 23077 |
rs34401764 | snp | A/C | 0.381697 | 0.212499 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323814 | TATCCTCAATAAACT[A/C]CCAGTCTTTATATTT | 23077 |
rs34408900 | snp | C/T | 0.347032 | 0.230401 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77254759 | CACTCTTCCTCTCCC[C/T]CTCCCACTATCCTTA | 23077 |
rs34441629 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228727 | TGTGTGTGTGTGTGT[-/GT]ATACCATGTAACACT | 23077 |
rs34454090 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77304222 | AAGATGTGGAATCAA[-/C]CCTACGTTTCCATGA | 23077 |
rs34471934 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118103 | TCCACTGAAAGTTGT[-/C]CCCTGTATGTGATGC | 23077 |
rs34474844 | snp | C/T | 0.0502116 | 0.150282 | missense | MYCBP2 | GRCh38.p7 | 13:77125461 | CATGTCCCTTCAGAA[C/T]TGGTTACCTGGTACA | 23077 |
rs34501650 | snp | C/T | | | splice-acceptor-variant | MYCBP2 | GRCh38.p7 | 13:77205599 | AGGTATCAAGACAAC[C/T]TAAAACAACAAAGAA | 23077 |
rs34552429 | in-del | -/G | 0.123798 | 0.215808 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77245605 | ATACTGGGGCCTGTT[-/G]GGGGGTGGGGGCTAG | 23077 |
rs34573526 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285659 | GCGCGGTGGCACATG[-/C]CCTGTAATCCCAGCT | 23077 |
rs34596822 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77116354 | ACTAGTGGGATACAT[-/G]GGTAGTGAGGTTCAG | 23077 |
rs34642345 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77174584 | AAATATACTGAAATT[-/C]CTTTGTCATATTTAC | 23077 |
rs34693218 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77088613 | AGTAAAGCAATACAG[-/C]AAATAAATTTCTTTA | 23077 |
rs34700794 | snp | C/T | 0.0692936 | 0.172758 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77089003 | AGAAAGCTCAGGAGA[C/T]GGATGTCTCAAAAGG | 23077 |
rs34714783 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77275514 | TATGTCACATCTTCA[-/G]GGGAGCCTGTTAAAG | 23077 |
rs34721563 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77093638 | TAAGCTAAAATATTT[-/C]CCAGTGTTGTAGTAG | 23077 |
rs34774363 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77306332 | GAATAGTTATCTCAT[-/C]TACTAAGTAGAAAAC | 23077 |
rs34781979 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77132246 | CTATTAACAAAATCA[-/G]GGAAATCTGGGGTAT | 23077 |
rs34801381 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77269255 | AACACTGTTTCCTAG[-/C]AAAGTACTGAATCTA | 23077 |
rs34811244 | in-del | -/A | 0.375 | 0.216506 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77153088 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23077 |
rs34819956 | in-del | -/A | 0.496034 | 0.0443518 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315914 | GCAAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23077 |
rs34822952 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77096299 | AGTATAGCTCCAAAT[-/G]GGAATAAAATACCTT | 23077 |
rs34855868 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77199244 | AAGCGCAAGGGGTCA[-/G]GGGAGTTCCCTTTCC | 23077 |
rs34873638 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77191171 | GCTTCACAAAGCTAT[-/G]TGAGGGCATCAAATC | 23077 |
rs34902275 | snp | C/T | 0.495671 | 0.0463237 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77287354 | AATGCCGGGCTAATT[C/T]TTGTATTTTTAGTAG | 23077 |
rs34930501 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77047383 | GTGAAGATTAAGTAT[-/C]CCTGGCACGAGAAGG | 23077 |
rs34982494 | snp | A/G | 0.0500534 | 0.150071 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77158073 | AATGAGAAAGAGCTA[A/G]ACCCTTTCCAAGAAT | 23077 |
rs35000423 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124673 | TATGACACTATTGTT[-/C]CTAGTGGTGAGCACA | 23077 |
rs35039431 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77313156 | TAAATTGGAAAATAA[-/T]TTTGAACTAAATGAC | 23077 |
rs35045084 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77110785 | CTACGTTGAAATATT[-/G]GGGGGCGGGTTCCCC | 23077 |
rs35046756 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77282427 | TGAAACTCCATCTTG[-/A]AAAAAAAAAAAAAAA | 23077 |
rs35064638 | in-del | -/G | | | frameshift-variant | MYCBP2 | GRCh38.p7 | 13:77095456 | TGGAATGGCTTTGCA[-/G]GGATGGTAACACAGA | 23077 |
rs35072238 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77299267 | TTTATCTAATGGAAC[-/T]TTCTTTAAAGTTCAA | 23077 |
rs35104501 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77104553 | GACGCCTAGAAGAGG[-/C]CCAAAGCCCTAGGAC | 23077 |
rs35130477 | in-del | -/G | | | intron-variant, upstream-variant-2KB | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77325162 | CAGCTTTACAACTGT[-/G]CTCCAACAGATAAGC | 23077 |
rs35143476 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77309788 | TTATCTTTATAAATT[-/G]GAAAGTTTAACTCTA | 23077 |
rs35170962 | in-del | -/G | | | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77327086 | GGGGCTACCCGCAAT[-/G]GGGAAGCTGCCGGCC | 23077 |
rs35187575 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77132940 | AAATCAATCAATGTT[-/C]CCCCAGGTATGCAAT | 23077 |
rs35203646 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77305949 | CTATACTGAATGTTG[-/A]AAAATTAAGTATTTC | 23077 |
rs35205263 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77310189 | AAATAAAGCAATACA[-/G]GGGAACATAATAACC | 23077 |
rs35220692 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77322893 | TGGCCTCATTCATCC[-/A]AAAATATATCTATTC | 23077 |
rs35240082 | in-del | -/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77292355 | TTCTGGCAAATCAAA[-/G]GGAAAAACCACCTAA | 23077 |
rs35251022 | in-del | -/A | 0.495521 | 0.0471118 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77292530 | GATTTAAAAAAAAAA[-/A]GAGCACTCACAATAT | 23077 |
rs35258010 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260263 | TGCTCCTAGTGACAA[-/G]GATATGACAGAAAAT | 23077 |
rs35269001 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77239256 | TGAAATGTTAACACA[-/G]GGTAAAAGCCAATTA | 23077 |
rs35294755 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77129795 | TAAGTAGGAAAAAAT[-/C]TCATTTGGAAATGTT | 23077 |
rs35336825 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77140403 | ATATATTTTAACTCA[-/T]TTTCTAAATACTGAA | 23077 |
rs35357585 | in-del | -/A | 0.0554779 | 0.157039 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77185032 | AGATATGGCAACTGC[-/A]AATTTATTTTCTTGA | 23077 |
rs35361907 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77149022 | GGAGTATCTTTATTG[G/T]TTTTTCTCTCAATTA | 23077 |
rs35367462 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77311306 | GAGAATTATAATAAA[-/C]CCTAGAGTTTACAAA | 23077 |
rs35370785 | in-del | -/T | 0.455263 | 0.142713 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316952 | TGTTGTTTTTTTTTT[-/T]GTTTTGAGATGGAGT | 23077 |
rs35381054 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77092430 | CATCATTCGTCCTCT[-/A]AAAAAGTTTCAGTGG | 23077 |
rs35387778 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77305355 | ATGTTGTTTACCCAT[-/A]AAAAAAGAATGAAGT | 23077 |
rs35414125 | in-del | -/T | | | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77077930 | CATTGAGAATATGAC[-/T]TTTTTTTTTCAAGGA | 23077 |
rs35417490 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77060316 | AAGGATGGTTTACAA[-/G]GGATGGTTTGACATT | 23077 |
rs35429706 | in-del | -/A/AA/AAA | 0.575207 | 0.128873 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243965 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GACAACTGAGATATT | 23077 |
rs35442398 | in-del | -/T | 0.496279 | 0.0429702 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77299010 | GTATTCTTCATACTA[-/T]TTTAGGAAACCAACT | 23077 |
rs35480904 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323815 | TCCTCAATAAACTCC[-/G]CAGTCTTTATATTTA | 23077 |
rs35490744 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77185456 | TATAATTCAGTAATT[-/C]CCCTATACAGCTAAG | 23077 |
rs35501539 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77226966 | TAAATAGAGTGTGGT[-/G]TACCTACATTATATT | 23077 |
rs35513622 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77259651 | ATAATTAATTGCTAT[-/A]AAATGTTCTACAGGT | 23077 |
rs35529593 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77112374 | TTTATTTATATAATA[-/C]TATAATATATATTTT | 23077 |
rs35544131 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056405 | AGAGCTTAATAGAAC[-/A]AAAAGGGGCGATGAA | 23077 |
rs35558910 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77294675 | AGCACCAAAAAGTTG[-/A]AAAGGGATAGAGGTT | 23077 |
rs35579966 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77274768 | TACCATTCGCTTTTG[-/C]CCCCAATAGCCAGGG | 23077 |
rs35603351 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77218422 | GATCTTAGAATCACA[-/G]GTTAATGAGTCAAAA | 23077 |
rs35617211 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77314195 | TGTCCACTAGATTTA[A/C]CCATTCCCCAATGTA | 23077 |
rs35621206 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130459 | GAATGTGGGTACACA[-/C]CCCATCTACATAAAT | 23077 |
rs35622384 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77189387 | AACCAGTGAGTACCT[-/G]GGGAGTAGTCCAATG | 23077 |
rs35654512 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77137532 | CAAGGTAAGATGATC[-/A]GCTTGAGCTCAGGAG | 23077 |
rs35674265 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | MYCBP2 | GRCh38.p7 | 13:77055619 | TAGCCAGCTGGGTCA[C/T]TATAAAACCTCACAC | 23077 |
rs35687504 | snp | A/C | 0.132409 | 0.220618 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77114409 | TAACAAAAATTCAGA[A/C]CTGTCAGATAACTTA | 23077 |
rs35696375 | snp | C/T | 0.00845363 | 0.064462 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77045402 | GTGGGCATTTCTGCA[C/T]ACTCCACATCCCAGA | 23077 |
rs35722534 | snp | G/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77159890 | GCCTGACACATATTG[G/T]TTATTATATATCTGT | 23077 |
rs35725605 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77224112 | TTGCTGACATTTTTT[-/A]AAAATACAATTCACT | 23077 |
rs35728912 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77136232 | CACTTGTAGTGACTT[-/C]CCACGTGCACTGCAC | 23077 |
rs35730660 | snp | A/G | 1.64827e-05 | 0.00287073 | missense | MYCBP2 | GRCh38.p7 | 13:77067599 | GAATTGAAAATCATC[A/G]GAAGAGTAACTGTTG | 23077 |
rs35732884 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77121000 | TTTGATTTTAAATGG[-/C]ATCATTTGAGCAAGT | 23077 |
rs35755625 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77099612 | GCACATGAATGCCCT[-/G]GAAGCTGTTATTTAA | 23077 |
rs35813706 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77252309 | TCAATTTTTAGCTTA[-/G]GAGGGCTATATAAAA | 23077 |
rs35840160 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77065343 | CCCCCAGAAAATCCT[-/C]CCCACTTCTCATATC | 23077 |
rs35841677 | in-del | -/A/AA | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77248155 | TCAAAAAAAAAAAAA[-/A/AA]GAAGAAGAAAAGATA | 23077 |
rs35862305 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77235604 | TTTCAATTAGTCAAC[-/A]AAAATATACTACAAA | 23077 |
rs35863177 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251874 | AATCTCATTTCTTTT[-/C]CCCTCTGCTCTCCAA | 23077 |
rs35867297 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77224155 | CCATGCACAGCCTTT[-/A]AAAAGATAATTGCTA | 23077 |
rs35887505 | snp | A/C/T | 0.0109287 | 0.0731099 | missense | MYCBP2 | GRCh38.p7 | 13:77171531 | GGAGGTCCTTAGAGG[A/C/T]TCGAACGACAGTGCT | 23077 |
rs35906266 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77061322 | TTTCATTAAAGAACA[-/G]GGGAAAAATATGCTT | 23077 |
rs35933603 | in-del | -/T/TT | 0.375 | 0.216506 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77176019 | CTTTTTTTTTTTTTT[-/T/TT]AAATGAGTTAGGGCA | 23077 |
rs35936462 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251621 | TCATACTTTTAAATC[-/T]TTTTCCTGTTTTCCA | 23077 |
rs35941136 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77207133 | AACAAATACCCCATT[-/A]AAAAAAGTTTAAAGA | 23077 |
rs35963575 | in-del | -/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186802 | AGTTTATAGATTCAA[-/T]TTTTTTTTTTTTTTT | 23077 |
rs35967770 | snp | A/G | 0.0253123 | 0.109615 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77260546 | CTTTCCTTCCATCTT[A/G]ATTATCTTTTTAGGT | 23077 |
rs35971530 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77137351 | TCTCCCAAAAGCAGC[-/T]TCCTCAAATGAGCAA | 23077 |
rs35983395 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77268217 | ATGACCATACCACTT[-/G]GCCAAGTAAATAATA | 23077 |
rs35987325 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77209228 | AAAAGACAAGGTTCA[-/C]ACCAGCTGAACATCA | 23077 |
rs36022859 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77188583 | AGATATGCAACTCTT[-/G]CCACCTAGTTCCTCA | 23077 |
rs36038074 | in-del | -/G | | | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77083748 | AATAATATTAACTAT[-/G]GGAATAACTTTTTAT | 23077 |
rs36060071 | in-del | -/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77123168 | ATATTATCACCAATG[-/C]AACAGACTATTTGGG | 23077 |
rs36069703 | in-del | -/A | 0.432944 | 0.170387 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195591 | ACTCTTAAAAAAAAA[-/A]TAGTCCGAAATAATC | 23077 |
rs36079867 | in-del | -/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237356 | CACATATGTGTAAGT[-/G]CTCTGTACATGATTA | 23077 |
rs36099519 | in-del | -/A | | | frameshift-variant, utr-variant-5-prime | MYCBP2 | GRCh38.p7 | 13:77273633 | CATCCCAGTACTTCG[-/A]AACGGTGATTTCCAA | 23077 |
rs41287040 | snp | A/G | 0.0577274 | 0.159785 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77059507 | AATGGGATGGCCTGT[A/G]TCACTATATACTCAC | 23077 |
rs41287042 | snp | C/T | 0.000148328 | 0.00861056 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77062635 | TCCCATCCATCTCCC[C/T]GAGGAGAGACGATCT | 23077 |
rs41288244 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, missense | MYCBP2 | GRCh38.p7 | 13:77103284 | TGTAAATGCGCTCAC[A/G]AGAAGCAAGGTTGCG | 23077 |
rs41288246 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77180399 | AAAACCTTGTCTTTC[C/T]GATACTCTTAAAATT | 23077 |
rs41288248 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77272349 | TGGGAGGCTTTCCAT[G/T]AACGTAGTTCTTATA | 23077 |
rs41288250 | snp | A/G | 0.026636 | 0.112288 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77296695 | TATTAAAAGAAAAAT[A/G]GGAAAAAAATATGAA | 23077 |
rs41300580 | snp | C/T | 0.00102031 | 0.0225636 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77270248 | CAGAACACAATTCAT[C/T]ATGGTTATAACTCTG | 23077 |
rs41315022 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77075607 | GAAAGCCAATGTCAT[C/T]TGCAATTTTTTTCAC | 23077 |
rs41331347 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77197389 | CTTGATACATAGGCC[A/G]GAAATCTAGACATTT | 23077 |
rs41405744 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77197994 | TGAAGATAAGGTCCA[C/G]TACGTTGTTCACTAT | 23077 |
rs55641840 | snp | C/T | 0.195526 | 0.243993 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77047134 | TCTTCAAGGTGTTCA[C/T]AATCCAACATGGTGG | 23077 |
rs55694124 | snp | C/G | 0.0618563 | 0.164627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77109528 | AGACAATCAGAACAG[C/G]CTTGTGATATTGTTA | 23077 |
rs55705093 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77199787 | GCAGGGGCAGACTGA[C/T]ACCTCACACTGCCTG | 23077 |
rs55722951 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77200435 | TGTACCTGAAAGTGA[C/T]GGGGAGAATGGAACC | 23077 |
rs55738060 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77086632 | GTATTTTTTATTTAC[G/T]TTTTCTGTGTTGAAG | 23077 |
rs55745763 | in-del | -/CATATATATATATATATATATATGTATATA | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77294120 | ATATATATATATATA[lengthTooLong]TATATATATACATAT | 23077 |
rs55766121 | snp | C/T | 0.18134 | 0.240387 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77192940 | TCAAGGCCAGCCTGG[C/T]CAGCATGGTAAAACC | 23077 |
rs55766384 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323846 | CAAGTACTCACCTCC[A/G]CCCCTTCTATATTAA | 23077 |
rs55830830 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77234565 | TGAATAACATATTCT[A/G]TGACTACTACAGATA | 23077 |
rs55860268 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186823 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTCTTCC | 23077 |
rs55921143 | in-del | -/AA/AC | 0.356383 | 0.226236 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131517 | CACACACACACACAC[-/AA/AC]TTGAATAGTGTTCTT | 23077 |
rs55933412 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77255992 | TATAAAAATTGAGGG[C/T]AAGAAGTAGACATGC | 23077 |
rs55945000 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77185069 | TTAAGCAATATATCA[G/T]ATTTTCAACTAACAT | 23077 |
rs55980120 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77177435 | CAGCCTCAACCTCCC[A/G]GGCTCAAGTGATCCT | 23077 |
rs55988260 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323680 | TCTATCTTGCTCACC[A/G]CTACATCTTCAGCAT | 23077 |
rs56061545 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77203092 | TTCAATTAGGAAAAG[A/G]GGAAGTCAAATTGTC | 23077 |
rs56063348 | in-del | -/AAG | 0.422315 | 0.181128 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77222408 | AGTTGTGTTTTTAAT[-/AAG]AAGTTCAACTCAATG | 23077 |
rs56079411 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77101567 | GTGTTAGAAAGAATA[A/G]GCATTTGTATATCTT | 23077 |
rs56123412 | snp | A/G | 0.155987 | 0.23165 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77197707 | CAAAGAGATAGAAGA[A/G]AAAACTACAGGTATG | 23077 |
rs56126821 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77191323 | CTGTTTTCTCATGCA[C/T]TATCAAATTTAATAT | 23077 |
rs56131306 | in-del | -/T | | | utr-variant-3-prime | MYCBP2 | GRCh38.p7 | 13:77044902 | TGTCCTAACACAATG[-/T]TTTTTTTTTTTTTAA | 23077 |
rs56148247 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77265552 | TTGAAATACTTTTTA[A/T]ATAAACTATACTGTA | 23077 |
rs56164318 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316952 | ACTTCTTTTTTTGTT[G/T]TTTTTTTTTTGTTTT | 23077 |
rs56171857 | snp | A/C | 0.102014 | 0.201495 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77166238 | TAAATTTCTCTAAAA[A/C]TTAGATAAACATTTT | 23077 |
rs56175548 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77180487 | TTCACTTAGAAGTTC[G/T]TTTTTGAATTATCTG | 23077 |
rs56192033 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77155831 | CCTCCTTTGAGTCCC[C/T]GTAACAGGTAGCAAA | 23077 |
rs56192617 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77254049 | TGGTATATTACACAT[C/T]AGTTAACATGAATCA | 23077 |
rs56222821 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77194669 | CCTGGGACCTAGTTT[A/C]CTCATCCATAAAAGG | 23077 |
rs56237958 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055364 | CGAAAAGTTTGTTCA[G/T]GTTAAATAAAGAATC | 23077 |
rs56238720 | in-del | -/AAA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072315 | GAAAAAAAAAAAAAA[-/AAA]GAAATCAAATGGGAA | 23077 |
rs56243387 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77090493 | CTTAAATCTACTTTG[C/T]ATTTTAAATGAAAAA | 23077 |
rs56274460 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77061586 | ACTTTTTCCCCCTAC[C/T]ACACAAAGCCTCTTT | 23077 |
rs56327755 | snp | C/T | 0.136506 | 0.222754 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77048681 | ATAATACCATCTACT[C/T]GCAGATTGTAAAAAT | 23077 |
rs56380130 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77300393 | CACATAAAGAGAGGA[A/G]TGTGCATATATTACA | 23077 |
rs56389916 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77219768 | GGAGAGTTTGAAGAT[G/T]CGAGAAAAGGTGTGG | 23077 |
rs56392444 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77316950 | TGACTTCTTTTTTTG[G/T]TGTTTTTTTTTTGTT | 23077 |
rs56398190 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77314745 | AAGAGTGAACCCTAA[A/T]GTAAACTCTGGACTT | 23077 |
rs56654461 | in-del | -/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77312832 | TGGATTTCTTTTTTT[-/T]AAGGGCAAGGTTCTA | 23077 |
rs56688388 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243391 | GCCAAGGTGGGCAGA[C/T]CACCTGAGGTCAGGA | 23077 |
rs56702763 | in-del | -/C | | | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074012 | CACCGCCCCCCCCCC[-/C]TTTTTTTTTTAAAGA | 23077 |
rs56823359 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77088296 | GATGAACACAAAGTG[C/T]ATCTCAAGCTCTAGG | 23077 |
rs56870536 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186562 | TACAAACTACAGTCA[A/G]TTTTTGATAAATACA | 23077 |
rs56870798 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77163506 | TGGGGGGGTAAGAAA[A/T]TAAAACTTTAAACCA | 23077 |
rs56952443 | in-del | -/GT/GTGTGTGT | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056159 | TGTGTGTGTGTGTGT[-/GT/GTGTGTGT]TTTGCTTCCTTGAGG | 23077 |
rs56995938 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77247409 | ATGAGAACTACAAAA[C/T]ATTGCTGAAAGAAAT | 23077 |
rs57007653 | snp | G/T | 0.194619 | 0.243789 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276841 | TTTTTTTTTTTTTTG[G/T]AGAGATAGGGGTCTA | 23077 |
rs57012685 | snp | C/T | 0.0699556 | 0.173447 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77150693 | GGTTAAATAAACAAA[C/T]GCTGAAAACTAAAAT | 23077 |
rs57109608 | in-del | -/T | 0.0498117 | 0.149749 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77153752 | TAAACTTTTTTTTTT[-/T]AATTCACAGGAAGTT | 23077 |
rs57286952 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77289390 | CCAACTGAGGTTTAA[A/C]CCAGGGACAATGCTG | 23077 |
rs57296816 | in-del | -/AAAAAAAAAAAAAAAAAAAA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77068414 | ATAAACAGTAAAAAA[-/AAAAAAAAAAAAAAAAAAAA]GGGAGTAAAATACAG | 23077 |
rs57489746 | in-del | -/TAT | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266716 | TATTATTATTATTAT[-/TAT]GACCAAAGACATGGT | 23077 |
rs57687748 | snp | C/T | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131613 | AGGAAAATGTTAATT[C/T]TTCCAAAGCCCCAAT | 23077 |
rs57692611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77305912 | TTATCTATAAAAAAC[C/T]TACTTTTAACAGTGT | 23077 |
rs57794089 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080745 | CCAGGGGTTTGAGAC[C/T]GGCCTGGACAACATG | 23077 |
rs57962133 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77248200 | CAACACTAGATTGGG[A/C]AATAATTTCTTGGAT | 23077 |
rs58038293 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77265359 | CAGATAAACGCAGGG[A/G]TGAGGAGTGAAGCGG | 23077 |
rs58146723 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77310645 | AAGGAAATAAGAAAT[C/T]GAGTCTGAAATAATA | 23077 |
rs58279253 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77108708 | TAAGATACTTTATTT[-/A]TTTTTTTTTTTTTGA | 23077 |
rs58458985 | in-del | -/GTGT | 0 | 0 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228725 | TGTGTGTGTGTGTGT[-/GTGT]ATACCATGTAACACT | 23077 |
rs58762828 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228728 | TGTGTGTGTGTGTGT[-/GT]ATACCATGTAACACT | 23077 |
rs58763547 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050666 | TAAAAAAAAAAAAAA[-/A]TCACAGAATCCTTTT | 23077 |
rs58976857 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77177149 | GAAAAATGACAATAT[-/A]AAAAAAAAAAAAAAC | 23077 |
rs58988213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77280088 | TTGTTTGCTAAAAAA[C/T]CACTGCATCTCAGAA | 23077 |
rs59026944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77284753 | ATATATATCATTTAC[C/T]GAGCACTTCTTTCTG | 23077 |
rs59133504 | in-del | -/AA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072316 | AAAAAAAAAAAAAAA[-/AA]GAAATCAAATGGGAA | 23077 |
rs59321884 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77092716 | CAGGTGTGAGCCACA[G/T]CGCCTGGCCTCTATT | 23077 |
rs59485801 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77082050 | TCCAGGAACATCTAA[A/G]GAACTCTTAGATGAG | 23077 |
rs59543063 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77210365 | GCCCGGCTAATTTTT[C/T]GTATTTTTAGTAGAG | 23077 |
rs59611452 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77321150 | TAATCTGGTTTTTGA[A/G]AAAAAAGTGAGACTA | 23077 |
rs59629334 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77279505 | TATACCTTCATAAGA[A/C]TGATAAAACAAAAGA | 23077 |
rs59664570 | in-del | -/GGTGGGAAGAAAAC | 0.0414363 | 0.137845 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77085301 | AAAGACTGAGGACAT[-/GGTGGGAAGAAAAC]CAATTATTTCAAGTT | 23077 |
rs60048134 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055852 | CCTAAGTGCCAAGCA[C/T]TGTGCTAGAAGATAA | 23077 |
rs60183284 | snp | A/C | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77293167 | AGTTGAGGAACTTTT[A/C]TGAGTAATGAATTTG | 23077 |
rs60253657 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050788 | CATGAGATCTGCTCC[A/G]TCACAGCTAACTTCT | 23077 |
rs60362493 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77283768 | TGGGGTGGTGGCAAA[-/T]CACCTGTAGTCCCAG | 23077 |
rs60371737 | in-del | -/CA/CAC | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77070594 | ACACACACACACACA[-/CA/CAC]AAACTAATGAAGACA | 23077 |
rs60402163 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77176921 | AATTCAAATTAACTA[A/G]TGAAAGGAATCAAGT | 23077 |
rs60429544 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77279742 | TAAGCACTCATATTG[A/T]GCAAACTCACTTTAG | 23077 |
rs60594552 | in-del | -/A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77059074 | ATTTTTTTTTTTTTT[-/A/T]AAAAAGGTACCTTTG | 23077 |
rs60723031 | snp | A/G | 0.104149 | 0.203046 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77047045 | ATTTACTCAACAAAT[A/G]TTTACCGCATGCCTA | 23077 |
rs60832891 | snp | A/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77114176 | AGGTAACTGAATTAC[A/T]TTGCAAAAATAGACC | 23077 |
rs60862252 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77218347 | GAAATTCAATCCAGG[A/G]ACTAGATGAAATAAT | 23077 |
rs60927409 | in-del | -/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183570 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTATCAT | 23077 |
rs60949122 | snp | A/G | 0.078151 | 0.181571 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77263597 | TGTTCATTTTTAAGA[A/G]TATGAAAAATTGAAA | 23077 |
rs60998294 | in-del | -/A | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228522 | AAAAAAAAAAAAAAA[-/A]TCTGTTCAAGCTCAT | 23077 |
rs61074887 | snp | C/T | 0.0663309 | 0.169604 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074008 | ATCCCCACCGCCCCC[C/T]CCCCTTTTTTTTTTA | 23077 |
rs61307561 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77137924 | CCAACTCCCCCTTGC[A/C]CAACAAAAAAGTCTA | 23077 |
rs61365681 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77208491 | CACTGATGGGCAAAC[A/G]GTTAAGTATATTTGG | 23077 |
rs61400342 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77241857 | ATAGCTAGAAAAAAA[-/A]TATAATGATGGTTAA | 23077 |
rs61533929 | in-del | -/GTGT | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77056156 | TGTGTGTGTGTGTGT[-/GTGT]TTTGCTTCCTTGAGG | 23077 |
rs61681230 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77281201 | AAAAATATAGTCCTG[C/T]CAATATAGTATTATT | 23077 |
rs61749886 | snp | A/G | 0.0002143 | 0.0103491 | synonymous-codon, intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77081451 | TCGGGAATTGTCCAC[A/G]TGAACAGACACATAG | 23077 |
rs61749888 | snp | C/T | 0.000777316 | 0.0196991 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77140134 | ACGGATGCGAAGCCC[C/T]GCACTGTCCTTGGCC | 23077 |
rs61749889 | snp | G/T | | | missense | MYCBP2 | GRCh38.p7 | 13:77150846 | TCAGTATTAGAAGAT[G/T]CAGCTGTTACTGCAG | 23077 |
rs61749891 | snp | A/G | | | missense | MYCBP2 | GRCh38.p7 | 13:77169676 | GGAGCAGCATGGAAA[A/G]CAGACTGGAAGAACT | 23077 |
rs61749892 | snp | C/T | 0.00612851 | 0.0550154 | missense | MYCBP2 | GRCh38.p7 | 13:77180195 | CACAGGTGTTAGAGA[C/T]GAGGTGGGAGGAGAA | 23077 |
rs61749893 | snp | A/C | 0.057002 | 0.158908 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77260492 | ATCTTTAGAAATAAC[A/C]GAACTACTTCCATTA | 23077 |
rs61753807 | snp | A/G | 0.000924504 | 0.0214802 | synonymous-codon, intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77081939 | AATGTGATGAAAGAC[A/G]TTGCTCTGATGAAGG | 23077 |
rs61753808 | snp | A/T | | | missense | MYCBP2 | GRCh38.p7 | 13:77058343 | GACAGTGCTCTTCGT[A/T]TTTAACACCCCCGCA | 23077 |
rs61753809 | snp | G/T | 1.73486e-05 | 0.00294517 | missense | MYCBP2 | GRCh38.p7 | 13:77055738 | TATTGGATCAAGTAG[G/T]TCTTTTAGTACTATG | 23077 |
rs61753810 | snp | A/G | 0.000282212 | 0.0118754 | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77185256 | ATATCCTTGAGGATC[A/G]TTATCCAATTTCACC | 23077 |
rs61753811 | snp | C/T | | | synonymous-codon | MYCBP2 | GRCh38.p7 | 13:77180298 | ACGGAAGCTTGTCAT[C/T]CCTGAGATATTCTCT | 23077 |
rs61753812 | snp | A/C/G/T | 4.96047e-05 | 0.00497999 | missense | MYCBP2 | GRCh38.p7 | 13:77098116 | GGCTCTAAAGGCTTG[A/C/G/T]ATCCATCTCCTTTGA | 23077 |
rs61754786 | snp | A/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77270069 | ATATATGGCCCTGCA[A/T]AAAAAACAAAAGTTA | 23077 |
rs61962740 | snp | G/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77047004 | CAAACTGCAGCCCTT[G/T]GGTTTTTTCAAGGAA | 23077 |
rs61962741 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77066385 | CACATGCGGATAATG[C/T]GGAGCTTAACCGGAA | 23077 |
rs61962742 | snp | A/G | | | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77087217 | ACAGACATGGAAACC[A/G]AGGCCTACAAGTCAT | 23077 |
rs61962743 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77096946 | TTTACTGAAAATGCA[A/G]TCTTCTGATAAAACA | 23077 |
rs61963476 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77268779 | AGCAAAACTACAACT[A/C]CAAAAAAAAAAAAAA | 23077 |
rs61963477 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276678 | GGGGTTTTTTTTTTG[G/T]TAGAGATGAGGTCTC | 23077 |
rs61963479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77296343 | AAGGATCACTTGAGC[C/T]CAGGAAACTACTGGA | 23077 |
rs61964702 | snp | A/G | 0.5 | 0 | stop-gained | MYCBP2 | GRCh38.p7 | 13:77157998 | CATCCAGAAAAGACT[A/G]TTCATTGCTTTGGAT | 23077 |
rs61964703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195458 | AAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 23077 |
rs61964704 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77196845 | TCAGAGAAGAGGTTT[A/C]TAAATTTAAAAGTCA | 23077 |
rs61964705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77197383 | CAAGAAAAATGTCTA[C/G]ATTTCCGGCCTATGT | 23077 |
rs61964706 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77203420 | CAAATGGAAGAACAT[C/T]CCATGCTCATGGGTA | 23077 |
rs61964707 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77209743 | CAACTCAATACTGGC[A/C]ACTACGCCTTCTCAT | 23077 |
rs61964708 | snp | G/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77215573 | GGATTGGAAGTAGAA[G/T]TCACAGTGGGGTTCT | 23077 |
rs61964709 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77215989 | CCCAGTTAGTGTCTA[A/G]TACTATTCCCCACTA | 23077 |
rs61964710 | snp | C/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77240062 | TTTCTTGTTTTATCT[C/T]TATGGAAGTGTAAGT | 23077 |
rs61964711 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77258439 | CAACTCTAAATTGAT[G/T]GAAGCATCTTTAACA | 23077 |
rs61964712 | snp | A/T | 0.493881 | 0.054972 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267419 | AAAATAAAATTAAAT[A/T]AAATTAAATAAAATT | 23077 |
rs63356361 | snp | C/G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074003 | ATTCCATCCCCACCG[C/G/T]CCCCCCCCCTTTTTT | 23077 |
rs66461920 | in-del | -/A | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77250238 | AAAAAAAAAAAAAAA[-/A]TCATATCTCAGCAGC | 23077 |
rs66485461 | in-del | -/AC | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131518 | CACACACACAAACAA[-/AC]ACACACACACACACA | 23077 |
rs66498316 | in-del | -/T | 0.275999 | 0.248644 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160066 | TTCAAAATCACAAAC[-/T]TTTTTTTTTTTTTTT | 23077 |
rs66518252 | in-del | -/AA | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266767 | AAAAAAAAAAAAAAA[-/AA]CCCTGTAGACATATC | 23077 |
rs66822058 | in-del | -/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055146 | TTAAAAAAAAAAAAA[-/G]AAGAAGTAGTTAAAG | 23077 |
rs66822059 | snp | A/G | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77055146 | TTAAAAAAAAAAAAA[A/G]AAGAAGTAGTTAAAG | 23077 |
rs66928059 | in-del | -/AC/CCCC | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77167025 | CACACACACACACAC[-/AC/CCCC]CAAATGAAATAATTT | 23077 |
rs67001158 | in-del | -/TC | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323983 | CAATTATCCCCTCTC[-/TC]ACTTCTTCACTCTGT | 23077 |
rs67087305 | in-del | -/A | 0.154661 | 0.231107 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77223908 | TCACGAACTAAAACT[-/A]AAACTAAAACAAATG | 23077 |
rs67648208 | in-del | -/A | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77063581 | AAAAAAAAAAAAAAA[-/A]GACAACTGTTTTCAG | 23077 |
rs68000917 | in-del | -/CT | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323978 | CCTATCAATTATCCC[-/CT]CTCTCACTTCTTCAC | 23077 |
rs68089729 | in-del | -/T | 0.499998 | 0.000888493 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195025 | TTTTAAAAAATGTCC[-/T]TTTTTTTTTTAAGAA | 23077 |
rs68189974 | in-del | -/A | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77243621 | CCATCTCAAAAAAAG[-/A]AAAAAAAAAAAAAAG | 23077 |
rs71102722 | in-del | -/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160083 | TTTTTTTTTTTTTTT[-/T]GAGACGGCGTTTCAC | 23077 |
rs71102724 | in-del | -/A | 0.969169 | 0.0668053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77176642 | CTCTAAAAAAAAAAA[-/A]TGAAACACAAAAATT | 23077 |
rs71102725 | in-del | -/GA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77233877 | AGAGAGAGAGAGAGA[-/GA]AAGGAGCTTGGGCTT | 23077 |
rs71102727 | in-del | -/CACACACACACACACACACACA | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77245762 | ACACACACACACACA[-/CACACACACACACACACACACA]AAGGAAATAAAAACA | 23077 |
rs71102729 | in-del | -/A | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77275154 | TCTACCCTTTCAAAA[-/A]GGTTAAGAATCCAGG | 23077 |
rs71102731 | in-del | -/GAAAGGAAAGGAAAG | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285884 | GAAAGGAAAGGAAAG[-/GAAAGGAAAGGAAAG]CAAAGGAAAGCAAAG | 23077 |
rs71102733 | in-del | -/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77287205 | TCTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC | 23077 |
rs71102735 | in-del | -/C/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77299013 | TTCTTCATACTATTT[-/C/T]AGGAAACCAACTTTC | 23077 |
rs71102737 | in-del | -/AC | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77310787 | CACACACACACACAC[-/AC]CATATTTAGGTACAA | 23077 |
rs71102740 | in-del | -/T/TAACA | 0.00398564 | 0.0444627 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77318007 | TAACATAACATAACA[-/T/TAACA]GTGGGTCCCTTATTC | 23077 |
rs71203036 | in-del | -/A | 0.361684 | 0.223667 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072301 | ATTTCAAAAAAAAAG[-/A]AAAAAAAAAAAAAAA | 23077 |
rs71203041 | in-del | -/A/AA/AAA | 0.479177 | 0.0998894 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77248142 | ACTTAAAGTATAATC[-/A/AA/AAA]AAAAAAAAAAAAAAG | 23077 |
rs71203042 | in-del | -/TTTTAT | 0.00119737 | 0.0244387 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77264598 | AATATATGCTTATGC[-/TTTTAT]TTTTATCTCAAAGCA | 23077 |
rs71203043 | in-del | -/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77291324 | AGCTAAAACCACAAT[-/G]GGGAAACCCCTACTT | 23077 |
rs71203044 | in-del | -/A | 0.499354 | 0.0179596 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303771 | TACTGAAAAAAAAAA[-/A]CACTGAAAGTAAATT | 23077 |
rs71203045 | in-del | -/C | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77307654 | AAAAAAAAAAAAAAA[-/C]CTTCATTGTATTGAA | 23077 |
rs71434859 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77075381 | TATTTCATGGGCACA[C/T]ACATGACAGTATAAC | 23077 |
rs71434860 | snp | A/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130660 | TGAAGTGCTATGTTT[A/T]AGGGGAAAAATGTCT | 23077 |
rs71434861 | snp | G/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77159905 | TTTATTATATATCTG[G/T]TGAATTTATTTTTAT | 23077 |
rs71434862 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77190899 | ATTGACCTGCACTGG[A/G]ATATATACTGTTATA | 23077 |
rs71434863 | snp | A/C | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266454 | ATAGATTAAAAAAGC[A/C]ATATGTAGCATATGA | 23077 |
rs71434864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286099 | AGCAAGCCATCTGCC[A/G]AGAATAAGGTGAGAA | 23077 |
rs71704593 | in-del | -/ACACAC | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77227482 | CACACACACACACAT[-/ACACAC]ACACACACACACACA | 23077 |
rs71730224 | in-del | -/AC | 0.4944 | 0.0526182 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77245852 | TATATATATATGTAT[-/AC]ACACACACACACATA | 23077 |
rs71749271 | in-del | -/A | 0.0407008 | 0.136725 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77070728 | TTTACATAGAAAAAG[-/A]AAAAAAAAAAAAAGA | 23077 |
rs71795907 | in-del | -/GTAT/TA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071238 | TATATATGTGTGTGT[-/GTAT/TA]ATATATATATATGCA | 23077 |
rs71814048 | in-del | -/CA | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071272 | ACGTGTGTGCACACG[-/CA]CACACACACACACAC | 23077 |
rs72339555 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77228692 | CTAAGATGAATATGT[-/TGTG]TGTGTGTGTGTGTGT | 23077 |
rs72628060 | snp | C/T | 0.110519 | 0.207473 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77087243 | GTCATACAACTACAA[C/T]AGGGTAGAAATGAGG | 23077 |
rs72628061 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77122428 | AGTCCTTGGCCGGTC[A/G]CGGTGGCTTACGCTT | 23077 |
rs72628062 | snp | A/T | 0.202959 | 0.245534 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77239836 | AATAAAAATATTTTT[A/T]AAAAAGCAAAGGTAA | 23077 |
rs72628063 | snp | A/T | 0.202651 | 0.245475 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251081 | TATTAATAGTAGAGT[A/T]TACTCCGGAATGATT | 23077 |
rs72628064 | snp | C/T | 0.223522 | 0.248594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77269609 | CTAACCTGGGTGACA[C/T]AGCGAGATTCTGTCT | 23077 |
rs72628065 | snp | A/C | 0.191775 | 0.243125 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77291244 | ACAGACATTTCACAT[A/C]AAAAAAATAAGAATG | 23077 |
rs73223407 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77220433 | GTGACAGAATCAGGA[C/T]CCAACCTAGAGACTG | 23077 |
rs73223408 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77221101 | CCAGGTTCGATGACT[A/G]TGTAGCATCTACCAG | 23077 |
rs73223410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77227926 | GAAACATTTTGTTCA[C/T]TGAAACAAACTGTAA | 23077 |
rs73223412 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77229373 | TTGAAGGGTTAAGGG[G/T]TTAAGTAACCAGCCC | 23077 |
rs73223415 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77235117 | TCTGATTATCTTTTA[A/T]TTAGCAGACACTAGG | 23077 |
rs73223416 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237808 | GGTTATGCTGATCTA[C/T]TTTTTCTTACTTATA | 23077 |
rs73223419 | snp | A/G | 0.079617 | 0.182947 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77242079 | TATATTTATCTTTGC[A/G]TATTCAAATACCAAT | 23077 |
rs73223420 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77248581 | GATACTATCTCACAC[A/C]CATTAGGATGCCACT | 23077 |
rs73223421 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77249719 | TTTTAATGGAAATAG[C/T]GTTGGAGAGATCCAG | 23077 |
rs73223422 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251073 | GAAAAAAATATTAAT[A/C]GTAGAGTATACTCCG | 23077 |
rs73223423 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251875 | AATCTCATTTCTTTT[A/C]CCTCTGCTCTCCAAA | 23077 |
rs73223424 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77252019 | CCTTCAAAAATTCAG[C/T]TCAGAAGTCATTCCC | 23077 |
rs73223428 | snp | A/G | 0.0590799 | 0.161399 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77260600 | GCTCTTAGCTTTAAA[A/G]AAGAAATTAGATTAA | 23077 |
rs73223429 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77266108 | ATAAAACAGCTGTAG[A/G]CACATATTTTCAAAT | 23077 |
rs73223430 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267074 | TAATATTGCTACTAT[A/G]AAATTATTGACAGAC | 23077 |
rs73223432 | snp | A/G | 0.100944 | 0.200705 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77268473 | ATTACTGAGAAACTA[A/G]TTTGTTATCTAAAAT | 23077 |
rs73223435 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77274841 | TCACTCCTTTGTTAA[C/T]TTCTTCCTCCCTTCT | 23077 |
rs73223441 | snp | G/T | 0.100944 | 0.200705 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285987 | AAGAAAAAGAAAAGG[G/T]TCCCACTCTAAAACA | 23077 |
rs73223442 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77288547 | TCCCCTTTTCTATAC[C/G]TCACTATTTTTTGAG | 23077 |
rs73223446 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77295107 | GGAAGGCAGAAGCAA[G/T]AGCTGAAAATATGGG | 23077 |
rs73223451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77303571 | AAAAACAAACAACTA[A/T]GAAATTCCCAAATGT | 23077 |
rs73223454 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77308889 | TATCTACCAACTCCC[C/T]ATCCATCACTGGTGG | 23077 |
rs73223455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77310587 | ATGATTATAGACACA[C/T]ATGATATCAAACAGT | 23077 |
rs73223457 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77311506 | TACATTGAGGAAAGA[C/T]AAGGACAACTGAATG | 23077 |
rs73223462 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77314975 | TTATCAGAGATCCCA[C/T]AGACCTTAAAGGATA | 23077 |
rs73223464 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315017 | CTATGGATAACTTCA[C/T]GCTAAAAACTTCAAC | 23077 |
rs73223466 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315081 | AAAAAATACAAGTTA[A/C]CAAAATTGACATGAA | 23077 |
rs73223468 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77315082 | AAAAATACAAGTTAC[A/C]AAAATTGACATGAAT | 23077 |
rs73223469 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77317758 | CCTGGTCCACATGGT[A/G]AAACCCCGTCTCTAC | 23077 |
rs73239432 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77050254 | ACTTGCACTCTGATA[A/G]GCAGCAGATGGCAGT | 23077 |
rs73239434 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77053494 | TGCAGAGGTTATAAA[C/T]GGTCGTTCACCAGCT | 23077 |
rs73239435 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77053653 | ATAATGTTTAGTACA[C/T]GAAACACACAGAAAT | 23077 |
rs73239440 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77059855 | ATACACTCTCGACTA[A/G]TATTTTTTTTCAGTG | 23077 |
rs73239442 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77067081 | TAATTTTCATTTTTA[C/T]ATAGTCAAATCTATA | 23077 |
rs73239444 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071500 | AGGAAAAACCTGATC[A/G]TCTACAAAACCAAAA | 23077 |
rs73239445 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77072552 | GGGAAAGAAATAAAG[A/T]TGTGATTATTAAAAG | 23077 |
rs73239447 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77073025 | ATACCATGCTATTCA[A/T]CTGTTTAAAGCATAG | 23077 |
rs73239448 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77073026 | TACCATGCTATTCAT[C/T]TGTTTAAAGCATAGA | 23077 |
rs73239449 | snp | C/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77073899 | TAAGAAAACCCCTGA[C/T]ACATATCATGTTCAC | 23077 |
rs73239451 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080289 | CAGGTTATCTGAGAC[A/C]CAATCCTACCACTGT | 23077 |
rs73239452 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77082187 | GTAACTTCTTTGGAA[C/T]AAGGTAAATTCTAAG | 23077 |
rs73239454 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77085049 | TGTTTTAAATATTTT[G/T]CCCAGCTTTTTGTTA | 23077 |
rs73239455 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77085216 | CAACTCATTTGGAAG[C/T]GTTACTTAATTTCCC | 23077 |
rs73239456 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77091871 | TCCTAAGGGGTAATA[A/G]TAACCCAATGAGAAT | 23077 |
rs73239458 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77092330 | AGTCAACAAGTCACA[C/T]TTATTTTTCCTACAA | 23077 |
rs73239462 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77095892 | AAATCATTTCAGTGC[A/G]TGTATTCAGTGAAAT | 23077 |
rs73239463 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77097064 | GAGATGCCCTGTGTG[C/T]ATGGGCATGCCACTG | 23077 |
rs73239464 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77101107 | ATTAATCTGACAGCT[A/G]GAGACATGTTTATCA | 23077 |
rs73239466 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77104339 | TATGAGTATATATTA[C/T]GTGTTAGATACTGTT | 23077 |
rs73239467 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77104397 | AGGAACAAAGTCCCT[A/G]TTCTCACAGAGTTTA | 23077 |
rs73239468 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77104398 | GGAACAAAGTCCCTA[C/T]TCTCACAGAGTTTAT | 23077 |
rs73239478 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77113456 | CCATAACCTAGCACA[C/G]AGTAGATACTTAACA | 23077 |
rs73239480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77113659 | CATCAGCATTCTTTG[C/T]GGTTTGAATTCCTAG | 23077 |
rs73239482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77117838 | AATGAAGGACTAGAG[A/C]AATCCTAAAAGACAG | 23077 |
rs73239485 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118785 | TTATGTATGGGAGAA[C/T]GAAGACTCTATGAAG | 23077 |
rs73239487 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77119700 | TTAAAAGCTTGTTAA[A/C]AAGAGTAGGCTTATT | 23077 |
rs73239488 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77123660 | ATGAGTAAAAAGTTG[C/T]ACAGCTGGGATCAGT | 23077 |
rs73239490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77124769 | ATGTGGTCTCAACTT[C/T]GAAGAACAAATTTTT | 23077 |
rs73239492 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77127579 | AACCATAAAGAGACA[C/T]ACATGCAAACATTAG | 23077 |
rs73239494 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77130729 | CTTGGTCAATGGGTT[C/T]TTCTCCCTTACAAAG | 23077 |
rs73239495 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131939 | CATGCCAAATGCTCA[C/T]GCAAATAAAAGAAAA | 23077 |
rs73239496 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77133818 | TTCTTCAAGTCCTCC[A/T]CAAATGTCACTTAAG | 23077 |
rs73239498 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77144291 | TTAATGCACTAATTA[A/C]ATACTCATTATGAAA | 23077 |
rs73239499 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77144916 | GATCCAAAGCTAGTC[C/T]CTCCCCTTGTGCTGT | 23077 |
rs73239500 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77146547 | GGAGATTTGTAACTC[A/G]TATAACCCAAAGGTG | 23077 |
rs73241403 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77151163 | GGTGTAAAAACAAGG[C/T]CTCATAGTTTTGGAA | 23077 |
rs73241408 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77156583 | TACTCTGCCATCCTG[C/T]AAGCCTGGAAAAAGC | 23077 |
rs73241409 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77159623 | CTGTTTTCCTTACAA[C/T]ATCTGGTTGTTTGAT | 23077 |
rs73241411 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160553 | TTCCCTTCTGAGTCT[C/T]CAAGAAGTCACAAAA | 23077 |
rs73241412 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77160629 | TACTGATTTCGAAGT[A/G]TAATTATAAAAACAG | 23077 |
rs73241414 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77162122 | CATACAGTTTAATAT[A/G]TAAGATACTTCCAGT | 23077 |
rs73241415 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77162591 | TCAACAGCCTATGTG[C/T]TGTTCTAGAAACTTG | 23077 |
rs73241417 | snp | A/C | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77167023 | CACACACACACACAC[A/C]CACCAAATGAAATAA | 23077 |
rs73241418 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77170522 | GCTTTCCAGGTGGTT[C/T]TGATGTTAAACTAGG | 23077 |
rs73241420 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77171413 | TTGTATAATAGAAGG[A/C]TCCTCTTCAATAATT | 23077 |
rs73241423 | snp | A/C | 0.0577619 | 0.159827 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77171448 | GCAAAAATTTAGTGA[A/C]TAAAGAATCTAAAAT | 23077 |
rs73241425 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77173703 | ATGACTACCTAAGAC[A/G]CCAGCTTTGCCGCTA | 23077 |
rs73241432 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77182906 | AAGATTTTTTTGTAA[A/G]TATCTTTTTATCAGA | 23077 |
rs73241434 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183051 | TTTTTTCAGTTAACA[A/T]GGTAAATTACATCGA | 23077 |
rs73241437 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183244 | TAGGATAAAGCTAAA[C/T]TCATAAAATTAGTTG | 23077 |
rs73241439 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77186786 | CAGAGCTCCTGAAAA[C/T]GAGTTTATAGATTCA | 23077 |
rs73241440 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77188002 | CTTGAACTCAGGACG[C/T]GGAGGTTGCAGTGAG | 23077 |
rs73241442 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77188355 | AACATCTTACACCCC[G/T]TATCTCATTAGAAAT | 23077 |
rs73241448 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195287 | GGTCTTTCATTCACC[A/T]AATCTCTTAGATAAA | 23077 |
rs73241450 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77195292 | TTCATTCACCTAATC[G/T]CTTAGATAAAAAGTC | 23077 |
rs73541756 | snp | A/C/T | 0.00856213 | 0.0648713 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77082003 | CAGCACCTAAAAAGG[A/C/T]GATATATAAGCAATA | 23077 |
rs73541767 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77103795 | TCTCAGAATGGACTC[A/G]GGGTGACACTGTGTT | 23077 |
rs73541771 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77117067 | TTCCCTTTGTCCTTA[A/C]CTTTAAAACTTCTTG | 23077 |
rs73541773 | snp | C/T | 0.0185622 | 0.0945332 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118308 | AAAGCTTCAGAAATG[C/T]TTGATGAGGCAGGTA | 23077 |
rs73541775 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77118892 | CAACAATGACTAATA[A/C]CACCCTGCCTCATCG | 23077 |
rs73541776 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77119552 | TTTTAAGAAAAAAAA[A/T]CTTACAAAAAACAGC | 23077 |
rs73541786 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77131557 | TTGAATAGTGTTCTT[C/T]GGAAATTTAGAAATG | 23077 |
rs73543851 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77138764 | AGAGAGTCAAAATTA[A/G]ACAGAACACACAGAA | 23077 |
rs73543856 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77149229 | CTTACCAATGTGAAT[C/T]GTTTTTCCTTTTCCT | 23077 |
rs73543867 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77161290 | ATTAGGTTGACGTAA[A/C]AGATCCAAAGGGGGT | 23077 |
rs73543871 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77163072 | TCAAAGAGCTGCATA[C/G/T]ACTACCATTGAATGG | 23077 |
rs73543874 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77163336 | TCTCATTTCCATACA[C/T]ATATACCAATATTAA | 23077 |
rs73543878 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77166968 | ACTTCAAAGACAAAA[C/T]ACACACATACACACA | 23077 |
rs73543881 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77170178 | GGGAAGATTAAACGA[G/T]GTAATATATGTAAAA | 23077 |
rs73543896 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77205751 | GAAGAATGCTTAAAA[C/G]CAATACAAATTATCC | 23077 |
rs73545866 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77230264 | TCACAAAAAAGTCAC[A/C]GTCTAAAAAATTTTA | 23077 |
rs73545869 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77230886 | CTTGGGGGCTTCATG[C/T]TGGTGCTCAAAAAGT | 23077 |
rs73545872 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77232536 | TCAAAGGACAACACC[A/G]AGCTAGATTCCTACT | 23077 |
rs73545874 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77234212 | ACAGCAGAACTATAG[C/T]TTCCTTGAGTTTTAA | 23077 |
rs73545880 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77235524 | GAGGTATGCAAAAAA[A/C]CAGATAATTAAAACC | 23077 |
rs73545888 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77237393 | AATAGAGTAAGATAT[C/T]AGACTATTAACATTT | 23077 |
rs73545889 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238310 | GGACTCTCCCATGTA[A/G]GCCAGGACATGGGTT | 23077 |
rs73545891 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77247546 | TATCAAAATCCCAAT[C/G]ATGGTTTTTACAAAA | 23077 |
rs73545898 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77251460 | GCATGCTAATCCAAG[A/C]AATTATACAAAGAAA | 23077 |
rs73545899 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77259200 | AACCTAGGAGGCAGA[A/G]GTTGCAGTAAGCTGA | 23077 |
rs73545902 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77271059 | TTTTTTCCTAATGTC[C/T]GACTACTTTTTATAT | 23077 |
rs73547877 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77281380 | TCAAATCATCTACAA[C/T]AAATATGTATAATTA | 23077 |
rs73547880 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286344 | AAATCATTTTGAATA[G/T]CTCTGTTTAGAAAAA | 23077 |
rs73547882 | snp | A/G | 0.167158 | 0.235875 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286454 | TATATCTACTATATA[A/G]AAAAAATATATATAA | 23077 |
rs73547884 | snp | C/G | 0.179105 | 0.239737 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77287696 | TACACAGCTGAGAGG[C/G]TTTGTAGTTCTATTT | 23077 |
rs73547886 | snp | A/C | 0.179744 | 0.239925 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77287743 | GCATACCTGCATCCC[A/C]GGTGAGGAGCACCTC | 23077 |
rs73547898 | snp | C/T | 0.178465 | 0.239547 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77313925 | TTCTACATCATATGT[C/T]ATCAGAGAAATGAAA | 23077 |
rs73547900 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77323452 | CCCAGAACATTCTTC[C/T]TCTACATCTGCCTCC | 23077 |
rs74095703 | snp | A/G | 0.029116 | 0.117091 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77286341 | ATAAAATCATTTTGA[A/G]TAGCTCTGTTTAGAA | 23077 |
rs74095710 | snp | A/G | 0.102726 | 0.202016 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77289694 | GATATCCTATCTAGT[A/G]CAAGGAAAATATCCT | 23077 |
rs74095711 | snp | A/C/T | 0.0807149 | 0.183963 | intron-variant, upstream-variant-2KB | MYCBP2 | GRCh38.p7 | 13:77293135 | AAGCCTGAAGACAGA[A/C/T]GCATTTGGGATTAGG | 23077 |
rs74095712 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77297470 | ATGAAGTCGGGGGGA[A/G]GAGGGAATGCAGGGA | 23077 |
rs74095713 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77308504 | CTCTCATCCATACAA[C/T]AGGGTGAAAACAGTA | 23077 |
rs74095715 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77312598 | AATACAAAGAGATAT[C/T]GCTGAAAAGACCAAT | 23077 |
rs74095717 | snp | C/T | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77326072 | GAAAACGCCACTTCC[C/T]TTGCCACTGTTGCAA | 23077 |
rs74096178 | snp | C/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77048959 | GATTTCCCCTGAAGA[C/T]ACTGCTTGCCTTAAA | 23077 |
rs74096179 | snp | C/G | 0.067446 | 0.170804 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77066456 | CAGCTGACTTTTTTC[C/G]TAGCAAGACTACAGG | 23077 |
rs74096180 | snp | A/C | 0.105214 | 0.203807 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071310 | ACACACACACACACA[A/C]ATCTTATCTAATCTT | 23077 |
rs74096181 | snp | A/G/T | 0.0991586 | 0.199366 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77077060 | TAGCCAGAAATTTCT[A/G/T]TAATAAGTTTCACAA | 23077 |
rs74096185 | snp | C/G | 0.097727 | 0.198275 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080059 | TAGCTTTGCACTGAA[C/G]AGTGAGTTCTAGCTA | 23077 |
rs74096188 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77086760 | TAGATTAATTTTTAC[A/G]TATTTTCTTTAGTTC | 23077 |
rs74096191 | snp | A/G | 0.077417 | 0.180873 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77116066 | CTATGTATGTTTCTG[A/G]GGCAAATCATTTATC | 23077 |
rs74098704 | snp | C/T | 0.134119 | 0.221521 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77145210 | CTGATGTCAAAGTCA[C/T]CAATGACCACCACGT | 23077 |
rs74098705 | snp | C/T | 0.157311 | 0.232183 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77145385 | TCAGTGTTTTGTTGC[C/T]TTCCCTTTTCTGACT | 23077 |
rs74098706 | snp | A/G | 0.158302 | 0.232576 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77146024 | TCTATACATTATTAT[A/G]TGACATCTCTATCGG | 23077 |
rs74098710 | snp | C/T | 0.0151786 | 0.0857842 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77164431 | AACCCTATCAAAAAA[C/T]ATCCAGTATTGGCCA | 23077 |
rs74098711 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77169886 | TTTTGAGAATACATG[A/C]CTTATCTCAACTAAT | 23077 |
rs74098713 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77170969 | CAGCAGTGAGATTAT[C/T]GGGATATTAACCCTA | 23077 |
rs74098714 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77179202 | TAAAATAAATTTTTT[A/T]AAAAAAGCAAAGATT | 23077 |
rs74098717 | snp | G/T | 0.15698 | 0.23205 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77198405 | TGTCCTTGGAAACCA[G/T]CATTATGAAGAAGAG | 23077 |
rs74098726 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77236120 | GGCCAGTTAAAAGGC[C/T]TTTTGCTGTCAGATA | 23077 |
rs74098727 | snp | C/T | 0.0209171 | 0.100105 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77257853 | AAGAAACAAATTTAG[C/T]AAAAACAACAAAAAG | 23077 |
rs74098729 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77268082 | AATGATTAAAAATAT[A/G]AGAACATTCCTCTCA | 23077 |
rs74239789 | snp | C/G | | | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074002 | AATTCCATCCCCACC[C/G]CCCCCCCCCCTTTTT | 23077 |
rs74341805 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77252722 | GCCTTTTGGGGTTTT[A/G]CCACTTCTAATCTAT | 23077 |
rs74350866 | snp | C/G | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77074010 | CCCCACCGCCCCCCC[C/G]CCTTTTTTTTTTAAA | 23077 |
rs74360470 | snp | A/G | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77257004 | CATCAGTAGATGAAT[A/G]GATAGAAAAATGTGG | 23077 |
rs74362800 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77306426 | ATTTAGGGGAGAGAT[A/G]AAAACAGATTTCTTA | 23077 |
rs74365765 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77114606 | TGTCCCACATAAGAA[G/T]GTGACTTATGAGTAT | 23077 |
rs74389773 | snp | G/T | 0.5 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77183571 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTATCATT | 23077 |
rs74400649 | snp | A/C | 0.0861826 | 0.188849 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77254914 | GTTCTATCCATGTTT[A/C]TGCAAATAACAATAT | 23077 |
rs74405297 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77087956 | CAGCTGATTTTAAAA[C/T]TTTTTTTTTGTAGAA | 23077 |
rs74405354 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77173944 | CAAGGCAACACCACT[A/C]TCTGAGTACAGTCTA | 23077 |
rs74425545 | snp | G/T | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77276676 | TGGGGGTTTTTTTTT[G/T]GGTAGAGATGAGGTC | 23077 |
rs74441316 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77187680 | AAAACTGTAAGTATC[A/G]TAAGAAACAAGCAAG | 23077 |
rs74451922 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77208192 | TGCTGAAGGCCTCAA[A/G]CCTCTTCAGAAAAAG | 23077 |
rs74474558 | snp | A/G | 0.00930457 | 0.06757 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77257621 | ATGTTGTTCTGAAAA[A/G]CTAATGAAAAGACAA | 23077 |
rs74480403 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77238391 | AGAAAAAGCTAACAT[C/T]ATTGAAGTTTAATTT | 23077 |
rs74493043 | snp | G/T | | | intron-variant | MYCBP2, MYCBP2-AS1 | GRCh38.p7 | 13:77080603 | TGATTATTTGGGACA[G/T]TCTGAAACTTATTTT | 23077 |
rs74555003 | snp | A/C | 0 | 0 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77188077 | CTCTGCCTCACCAAA[A/C]AAAAAAAAAAAAAAA | 23077 |
rs74594586 | snp | C/T | | | intron-variant | MYCBP2 | GRCh38.p7 | 13:77285613 | CCAACATGGAGAAAC[C/T]CCATCTCTAATAAAA | 23077 |
rs74623565 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77267429 | TAAATTAAATTAAAT[A/T]AAATTAAATTAAATT | 23077 |
rs74641692 | snp | A/G | 0.125528 | 0.21681 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77071867 | GGACTGAAATTATAC[A/G]AAGTATACAATACAG | 23077 |
rs74647809 | snp | A/G | 0.0341408 | 0.126114 | upstream-variant-2KB, nc-transcript-variant | MYCBP2, LOC107984564 | GRCh38.p7 | 13:77328208 | AAAATCCTCCTTAGT[A/G]TTTGAGAAGTGCAAA | 23077 |
rs74655610 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | MYCBP2 | GRCh38.p7 | 13:77151676 | TGTCTTATAAAAATA[C/G]CTTTTAGATATATTT | 23077 |