SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4788 | snp | A/T | 0.350611 | 0.228861 | synonymous-codon | NACA | GRCh38.p7 | 12:56712876 | AGAAGTTAAGGACAT[A/T]GAATTGGTCATGTCA | 4666 |
rs4901 | snp | A/C | 0 | 0 | synonymous-codon | NACA | GRCh38.p7 | 12:56713612 | GAAATCTAAGAATAT[A/C]CTCTTTGTCATCACA | 4666 |
rs4902 | snp | C/T | 0.452748 | 0.146265 | synonymous-codon | NACA | GRCh38.p7 | 12:56714419 | GGCAGCAGCTGAAAT[C/T]GATGAAGAACCAGTC | 4666 |
rs898609 | snp | C/T | 0.452598 | 0.146472 | intron-variant | NACA | GRCh38.p7 | 12:56713026 | TAATTTAACTCTCGC[C/T]GTATAGCATTGTGTT | 4666 |
rs1078604 | snp | G/T | 0.0955749 | 0.196603 | intron-variant | NACA | GRCh38.p7 | 12:56713370 | ggttctcaactaggg[G/T]gtagttaggtctccc | 4666 |
rs1466382 | snp | C/T | 0.451608 | 0.147832 | intron-variant | NACA | GRCh38.p7 | 12:56723050 | CATTATGTTTGGTAG[C/T]GTTTTCCTGTAATCG | 4666 |
rs1802304 | snp | C/T | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712517 | TGGAAGCAACTTTTT[C/T]TGGTGTCTCAAAGGA | 4666 |
rs1979325 | snp | C/G | 0.309648 | 0.24278 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728152 | AATTGTGAATATGTA[C/G]TTTTGTCTAAGGAAA | 4666 |
rs2290894 | snp | C/G | 0.456095 | 0.141508 | intron-variant | NACA | GRCh38.p7 | 12:56714911 | TATTTCTAGTGATTA[C/G]TCCTCATTTCTGGGG | 4666 |
rs2860482 | snp | A/C | 0.309894 | 0.242719 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712154 | GGAGACGGGGTTTCA[A/C]CGTGTTAGCCAGGAT | 4666 |
rs2926742 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACA | GRCh38.p7 | 12:56722442 | caggcatcccgaagt[A/G]ctgggattacaggca | 4666 |
rs2926743 | snp | C/T | 0.348303 | 0.229862 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720316 | ATGTAGCTACCTCTT[C/T]TTCATTATCTCCTAC | 4666 |
rs2926744 | snp | C/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718128 | AGCTGCAACTCCTCC[C/T]TCCCCAAAAGGAGGT | 4666 |
rs2926745 | snp | A/C/G | 3.92819e-05 | 0.00443164 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718026 | AGCTACCCCACCCCC[A/C/G]AAAGGGGCCCCCACA | 4666 |
rs2926746 | snp | C/T | 0 | 0 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717921 | AGCTGCAACTCCTCC[C/T]TCCCCAAAAGGAGGT | 4666 |
rs2926747 | snp | A/T | 0.445578 | 0.155722 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716147 | GTCTCTGCAGCACCC[A/T]CCCCACCAGTCTCTC | 4666 |
rs2926748 | snp | C/G | 0.476487 | 0.105846 | intron-variant | NACA | GRCh38.p7 | 12:56715628 | TTGTGTAATGTGGCC[C/G]GGACTACCCTGAGCC | 4666 |
rs2958127 | snp | A/T | 0.452794 | 0.146201 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720523 | TGTCAGACCCTACAG[A/T]GAAGACCATTTCTGT | 4666 |
rs2958149 | snp | A/G | 0.346118 | 0.230784 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716008 | GGGGGAATCAGAGGC[A/G]GCAGCTCATCCTCAT | 4666 |
rs2958150 | snp | A/G | 1.9595e-05 | 0.00313003 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717962 | GGGCCCCTTTGGGGG[A/G]TGGGGTAGCTAGACC | 4666 |
rs3214051 | snp | C/T | 0.456332 | 0.141164 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725452 | TTCTTACCCTTTAGT[C/T]CTTGTCACCACCCCC | 4666 |
rs3782232 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | NACA | GRCh38.p7 | 12:56722465 | GATGCCTGGGAGGGC[A/G]GATCACGAGGTCAGG | 4666 |
rs3837441 | in-del | -/ACAAAAAAAACAAA | 0 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56722704 | TCAAAACAAAACAAA[-/ACAAAAAAAACAAA]CCAAAGAAGACAATT | 4666 |
rs7133373 | snp | A/G | 0.0192285 | 0.0961483 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719388 | AGCACAGGTATTCTG[A/G]GGGGATGGAGCCACA | 4666 |
rs11171951 | snp | A/G | 0.451253 | 0.148334 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718853 | CTTTGGGGAAGGGCA[A/G]ATTCACCACTGAAGG | 4666 |
rs11171952 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | NACA | GRCh38.p7 | 12:56722877 | GCTCAATGCTTAGAA[A/G]GGAATGTTAAGGGGG | 4666 |
rs11171953 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | NACA | GRCh38.p7 | 12:56724579 | ATACATTCACTTGCC[C/T]AACCCGGAGATAAGT | 4666 |
rs11171954 | snp | A/C | 0.105362 | 0.203911 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725947 | cccccgccccccccc[A/C]aaaaaaaacacttct | 4666 |
rs11555457 | snp | G/T | 0 | 0 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725063 | AAGGGCTGCGGGGCG[G/T]GCCCAGAATCCGAGC | 4666 |
rs11555460 | snp | C/T | 3.29815e-05 | 0.00406075 | missense | NACA | GRCh38.p7 | 12:56714435 | TATCTTCTTAGCTGG[C/T]GGCAGCAGCTGAAAT | 4666 |
rs11555461 | snp | A/G | | | missense | NACA | GRCh38.p7 | 12:56714639 | TACCAGAGCTTGAAG[A/G]ACAGGATTCCACCCA | 4666 |
rs11555463 | snp | A/G | | | missense | NACA | GRCh38.p7 | 12:56713608 | GTTTTGTGATGACAA[A/G]GAGGATATTCTTAGA | 4666 |
rs11611171 | snp | G/T | | | missense | NACA | GRCh38.p7 | 12:56713594 | CTTGTAGACATCTGG[G/T]TTTGTGATGACAAAG | 4666 |
rs11613539 | snp | G/T | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712172 | tgttagccaggatgg[G/T]ctcaatctcctgacc | 4666 |
rs11614141 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NACA | GRCh38.p7 | 12:56715244 | ATCAATATAATTAGA[A/G]GATTCTCAATGATGA | 4666 |
rs11833256 | snp | A/G | 0.000235789 | 0.0108554 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718309 | GCCCCCTTGAGGGAT[A/G]GGGTAGCTGGACCTC | 4666 |
rs11834498 | snp | C/G | 0.00762007 | 0.0612533 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720061 | GTAGAAGGCTCTTTG[C/G]GAGCCACAGGTGCCA | 4666 |
rs11837790 | snp | A/T | 0.164873 | 0.23506 | intron-variant | NACA | GRCh38.p7 | 12:56723701 | GTGAGAATGAAAATT[A/T]CAGCCTGAAGATTTC | 4666 |
rs12317052 | snp | A/C | 0.0681886 | 0.171594 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728133 | AAGGACCAGAAATAG[A/C]CAATTTCCTTAGACA | 4666 |
rs12317155 | snp | A/G | 0.0681886 | 0.171594 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728132 | GAAGGACCAGAAATA[A/G]CCAATTTCCTTAGAC | 4666 |
rs12423816 | snp | C/G | 0.375 | 0.216506 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716026 | AGCTCATCCTCATCA[C/G]CAGGGGCAAGGGGTT | 4666 |
rs12822307 | snp | A/G | 1.97054e-05 | 0.00313884 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717824 | GGGCCCCTTTGGGGG[A/G]TGGGGTAGCCAGACC | 4666 |
rs12822513 | snp | C/T | 7.89796e-05 | 0.00628359 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717834 | GGGGGATGGGGTAGC[C/T]AGACCTCCTTTTGGG | 4666 |
rs12822848 | snp | G/T | 1.96926e-05 | 0.00313782 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717819 | TGTGGGGGCCCCTTT[G/T]GGGGATGGGGTAGCC | 4666 |
rs12822876 | snp | A/G | 0.000471568 | 0.015348 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717852 | ACCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs12822887 | snp | G/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717888 | TGTGGGGGCCCCTTT[G/T]GGGGATGGGGTAGCT | 4666 |
rs17118953 | snp | C/T | 0.0864633 | 0.189092 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721085 | GAAAAGCAGAACTCT[C/T]CTGAACTGAGTGGGG | 4666 |
rs28441189 | snp | A/C | 0.0290846 | 0.117032 | intron-variant | NACA | GRCh38.p7 | 12:56722705 | TCAAAACAAAACAAA[A/C]CAAAGAAGACAATTG | 4666 |
rs34031751 | in-del | -/C | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726923 | GGACCCCACCTTAAA[-/C]CCATGCTTTGTACAA | 4666 |
rs34332706 | in-del | -/T | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56711944 | GCCTAGTATAGTAAC[-/T]TTTTTTTTTTTTTTT | 4666 |
rs35908345 | in-del | -/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723558 | CTGTATTAATCCCTT[-/G]CAGCTGTTAAAATCA | 4666 |
rs36039765 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56721504 | GGGGAGGGGGAGGAG[-/A]AAAAAAGGTGAGTTA | 4666 |
rs56743414 | snp | A/G/T | 0.000726418 | 0.0190449 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718155 | AGCTGGGGTTGTGGG[A/G/T]GCCCCTTTGTGGGGT | 4666 |
rs58668145 | snp | G/T | 0.499968 | 0.00399348 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718164 | TGTGGGTGCCCCTTT[G/T]TGGGGTGGGGTAGCT | 4666 |
rs58799419 | in-del | -/A | 0.482609 | 0.0916147 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725947 | CCGCCCCCCCCCCAA[-/A]AAAAAACACTTCTTG | 4666 |
rs59501151 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725251 | GACAGTAGCGGCACA[A/G]AAAGTACTTACTGTG | 4666 |
rs59533878 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718031 | GGGCCCCTTTTGGGG[A/G]TGGGGTAGCTAGACC | 4666 |
rs61032015 | snp | G/T | 0.0015808 | 0.0280696 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718165 | GTGGGTGCCCCTTTG[G/T]GGGGTGGGGTAGCTA | 4666 |
rs61379639 | snp | G/T | 0.5 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56724161 | CTGAGCCCATTCCCT[G/T]CTGAGTTTTCCTATG | 4666 |
rs61754172 | snp | G/T | | | synonymous-codon | NACA | GRCh38.p7 | 12:56714614 | CACCTGGGCTTGTTG[G/T]GTGGTTGCCTGGGTG | 4666 |
rs61937760 | snp | C/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56716939 | TAGAGAGAAGAGTCG[C/T]TGTTGGGGCAATGGG | 4666 |
rs61937775 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NACA | GRCh38.p7 | 12:56724827 | CTCCTAATACTCACA[C/T]TGGCTGGGCTGGGGC | 4666 |
rs63502261 | in-del | -/T | 0.383632 | 0.211288 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726286 | TGGGCACTTCTTGGA[-/T]TTTTTTTTTTTTTTT | 4666 |
rs71081395 | in-del | -/TTGTGGGTGCCCCTTTGTGGGGTGGGGTAGCTAGACCTCCTTTTGGGGAGGGAGGAGTTGCAGCTGGGG | 0 | 0 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718216 | GAGTTGCAGCTGGGG[lengthTooLong]GCATGGGGGCCCCTT | 4666 |
rs71446568 | in-del | -/T | 0.5 | 0 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56711968 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 4666 |
rs71662623 | in-del | -/AAAACAAAACAAAA | 0.498133 | 0.030494 | intron-variant | NACA | GRCh38.p7 | 12:56722696 | ACTCCGTCTCAAAAC[-/AAAACAAAACAAAA]AAAACAAACCAAAGA | 4666 |
rs74526969 | snp | G/T | 0.00162443 | 0.0284531 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717334 | GAAGTGGGGTCCCCT[G/T]TGGGAGATGGGATAG | 4666 |
rs75059669 | snp | A/G | 0.00152408 | 0.027563 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721300 | AAAGGAACTTCTAAA[A/G]GGGTCGAGGCAATAG | 4666 |
rs75238599 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NACA | GRCh38.p7 | 12:56724875 | CCGACTTTGGGGTAC[C/G]AGGAGGGGAAAGACG | 4666 |
rs75617904 | snp | C/T | 0.00255784 | 0.0356704 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720283 | GCATTAGGAGAGCTT[C/T]TGAGAATGAGAGAGG | 4666 |
rs76076193 | snp | A/G | 0.0495374 | 0.149384 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716658 | TGCTGGGCCCTTTTC[A/G]GGGGATGGAGGAGTC | 4666 |
rs76163127 | snp | A/G | 0.00186151 | 0.0304515 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719836 | GAATTTTTAGGGGCT[A/G]CCTGGACTAACGGTA | 4666 |
rs76463302 | snp | C/T | 0.00364522 | 0.0425361 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719357 | TTTCAGGGGCCAGCA[C/T]TAAGGTAGCCAGAGG | 4666 |
rs76782323 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NACA | GRCh38.p7 | 12:56724358 | AAGCTGCAACCCCAT[C/T]CTCCTAAAAAGTGTA | 4666 |
rs77508410 | snp | A/G/T | 0 | 0 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719745 | AGCAAAGAAAAGCCT[A/G/T]GGGGAGCCTCTCCCT | 4666 |
rs77660658 | snp | G/T | 0.5 | 0 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712388 | AGTTTTTTTTTTTTT[G/T]GGTGTGGGGGGGTGG | 4666 |
rs78241008 | snp | A/T | 0.5 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56713787 | CCTTTCCCCAGGCTG[A/T]GAAAAGTTCATACAA | 4666 |
rs78652190 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NACA | GRCh38.p7 | 12:56715044 | AGTCCAATTATCCCT[C/G]TAAAGTTCTGTCAGA | 4666 |
rs78726726 | in-del | -/TG | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727354 | TTTTTTTTTTTTTTT[-/TG]AGACGGAGTCTCGCT | 4666 |
rs78882823 | snp | G/T | 0 | 0 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715936 | ATTCCAGCAGATTTA[G/T]GGGTGGGCATGTTGA | 4666 |
rs79407407 | snp | G/T | 0.000612892 | 0.0174949 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712600 | ATAGGCAAATCAGGA[G/T]AATTCAGGTCACTAA | 4666 |
rs79416939 | in-del | -/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727354 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 4666 |
rs79626244 | snp | G/T | 0 | 0 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726302 | TTTTTTTTTTTTTTT[G/T]TTGAGTCGCTCTGTC | 4666 |
rs80229810 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NACA | GRCh38.p7 | 12:56723049 | ACGATTACAGGAAAA[C/T]GCTACCAAACATAAT | 4666 |
rs111374332 | snp | A/C/G | 1.84032e-05 | 0.00303335 | intron-variant, splice-donor-variant | NACA | GRCh38.p7 | 12:56715869 | CAAACCAAGGCAAAT[A/C/G]CCCTTGTTGTTCTTC | 4666 |
rs111411917 | snp | C/T | 0.000483075 | 0.015534 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719077 | TTTCCAATAGGAGTA[C/T]CAGGGCCAGCAGAAC | 4666 |
rs111433500 | snp | C/T | 1.66283e-05 | 0.00288338 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720883 | GCCATGGGAGTCACA[C/T]AGTGGTAAGGAACAG | 4666 |
rs111519864 | in-del | -/TTCAACCTC | 0.00160901 | 0.0283181 | intron-variant | NACA | GRCh38.p7 | 12:56713710 | AAATAGTATCAGGTT[-/TTCAACCTC]TTCAACCTCTTTAGA | 4666 |
rs111596347 | snp | C/G | | | splice-donor-variant | NACA | GRCh38.p7 | 12:56724451 | GGGTAGGGAAACCTA[C/G]CTGTCTCAGCCTGGG | 4666 |
rs111651575 | snp | A/G | 0.00115637 | 0.0240176 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716177 | CAGATGCTGATTCAG[A/G]TTTAGGAAGGACCTT | 4666 |
rs111848322 | snp | A/G | 0.5 | 0 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717990 | ACCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs111991482 | snp | G/T | 0.000644069 | 0.0179338 | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712502 | CCAAGCTGCAGTTAC[G/T]CCTTTGAGACACCAA | 4666 |
rs112189772 | snp | A/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726639 | GGTGCAAAGGCACGA[A/T]CTCGGCTCACTGCAA | 4666 |
rs112233962 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725195 | TAACTCTCAGTCCCC[C/G]GGGCGGCTTAGCCCG | 4666 |
rs112667046 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727507 | GAACTCCTGAGCTCA[A/G]GCAATCCACCCGCTT | 4666 |
rs113615834 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718197 | ACCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs113647503 | snp | A/C | 0.0240643 | 0.107019 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725323 | AGAGCGTGACCCACG[A/C]CTGTTGCAGAAGGAA | 4666 |
rs113649210 | in-del | -/C | 0.5 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56722696 | GACTCCGTCTCAAAA[-/C]AAAACAAACCAAAGA | 4666 |
rs113748992 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726722 | GGATTACAGGCATGC[A/G]CCACCACGCCAGTCT | 4666 |
rs113809909 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56722696 | GACTCCGTCTCAAAA[A/C]AAAACAAACCAAAGA | 4666 |
rs113978151 | snp | A/G | 0.5 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56714865 | TAGTCACTAACTAGC[A/G]GGTACACATCTAGTA | 4666 |
rs114648947 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | NACA | GRCh38.p7 | 12:56713384 | GGGTAGTTAGGTCTC[C/G]CAGGAGATATATGGC | 4666 |
rs115011669 | snp | C/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725565 | GGTCCGCGAAGTGGC[C/G]ACTGCGGTATTAAGT | 4666 |
rs115327810 | snp | A/C/T | 0.000781402 | 0.0197528 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720928 | GGAGGGCTGGGGGTG[A/C/T]CTTTTGGATTAGGGA | 4666 |
rs117279942 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NACA | GRCh38.p7 | 12:56723693 | CCAAAAAGGTGAGAA[C/T]GAAAATTACAGCCTG | 4666 |
rs137880788 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725271 | TACTTACTGTGCAGG[A/G]AACGCGGAACCAAGA | 4666 |
rs138027303 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722145 | TTAATATCAAGTATT[A/G]AAGTCACTTAGCTTC | 4666 |
rs138705468 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACA | GRCh38.p7 | 12:56722406 | GAAGAAGAGAATTGG[A/G]GAGCCTGTAACAGTG | 4666 |
rs138803259 | snp | A/C/G | 0.000719122 | 0.0189487 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716046 | GGCAAGGGGTTTAGA[A/C/G]GGTGATTCCAACACC | 4666 |
rs138834097 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56724921 | CACTTGCTTGTCACA[A/G]GGAGAACGGTGTTAC | 4666 |
rs139390548 | snp | G/T | 0.00021615 | 0.0103937 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720092 | TAACCAAGGCAGCAG[G/T]GGAAGTTGGTTCTAT | 4666 |
rs139726606 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726088 | GCTGACTCCATTCTT[G/T]GGAGGTTTTCTGGTT | 4666 |
rs140007338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723677 | TGAAATTTAAAAAAA[A/C]CCAAAAAGGTGAGAA | 4666 |
rs140160509 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725741 | TGGACCCTCTCCCCC[C/T]CCATCAACAACAACA | 4666 |
rs140274839 | snp | A/G | 0.000233555 | 0.0108038 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719491 | GGAGCTAAAGAGACA[A/G]TTCCTTCTAGAAAAG | 4666 |
rs140340441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713331 | CTCACAGTAGAAAGA[A/G]TAGTTGTTTAGGTTT | 4666 |
rs140391076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56721711 | TCTACCAAAGTAAAC[C/T]AACTATTTTAGGGTG | 4666 |
rs140448348 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon | NACA | GRCh38.p7 | 12:56713086 | TTCACTCTCCTCTTG[G/T]ACAGTTGGAGTCTGT | 4666 |
rs140567329 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NACA | GRCh38.p7 | 12:56723783 | TTTCATTACCTCCTC[C/T]TAAGTTTTCTACAGA | 4666 |
rs140966189 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACA | GRCh38.p7 | 12:56715430 | TCCCTGGGCAACTGG[C/T]CATTACTAAGTCTAA | 4666 |
rs141524946 | snp | C/G | 0.000153988 | 0.00877328 | missense | NACA | GRCh38.p7 | 12:56724482 | GCTGCGGCAACTCCT[C/G]CTCTGTAGCAGGGAC | 4666 |
rs141981954 | snp | A/G | 0.000270796 | 0.0116329 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716077 | AGCCCAGGAGAGGAC[A/G]GCAGAAATTGCTGTT | 4666 |
rs142227224 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727752 | TAGGAGAGGCAATAT[G/T]GTGGAGTCATTAAAG | 4666 |
rs142292790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACA | GRCh38.p7 | 12:56724846 | CTGGGCTGGGGCCTC[C/T]TGGACTACGTTTGCC | 4666 |
rs142751283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724952 | AGGTTCTAAGGCTGT[A/G]ACCCCTTACCCTTTT | 4666 |
rs142966502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723009 | TCAACTAGTTTTTCC[C/T]GGAGAGTGGGTAGGC | 4666 |
rs143298780 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | NACA | GRCh38.p7 | 12:56714647 | ATCCTGTTCTTCAAG[C/T]TCTGGTACTGATTCA | 4666 |
rs143331141 | in-del | -/C | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727579 | ACCTGGTGTGGCCGC[-/C]TTTTAAGGGAAGCAG | 4666 |
rs143515670 | snp | A/G | 0.00273791 | 0.0368979 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718933 | GTCACAGCTGAGGGA[A/G]TAGGGGCCCCTTTGG | 4666 |
rs143592453 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56724772 | CCCGGGCTGGCTCTC[G/T]ATCATGGGAGACTTC | 4666 |
rs143658170 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACA | GRCh38.p7 | 12:56722150 | ATCAAGTATTAAAGT[A/C]ACTTAGCTTCTTTAT | 4666 |
rs143746561 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56715293 | TTTCCAAACATAATT[C/G]ACATAAATTTCTTTC | 4666 |
rs143762189 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | NACA | GRCh38.p7 | 12:56723751 | ACTGACTCAGAAAGG[C/G/T]TATCATTTTAAGAAC | 4666 |
rs143879365 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725552 | GACTCCGCCCTCCGG[G/T]CCGCGAAGTGGCGAC | 4666 |
rs143904231 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725824 | TTCAGATTATAAATT[G/T]AATTCGATTTTTCTT | 4666 |
rs144176092 | snp | C/T | 0.000183271 | 0.00957088 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719573 | CCCCGGCAGGGTCAG[C/T]ACTTTCCAAAGGAAA | 4666 |
rs144343322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56723974 | CGACCTAGGACGACT[A/C]TGGGGCCCAGTAGGA | 4666 |
rs144418941 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NACA | GRCh38.p7 | 12:56722450 | ATCCCAGCACTTCGG[A/G]ATGCCTGGGAGGGCG | 4666 |
rs144522448 | snp | A/C/G | 0.000282716 | 0.0118862 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716452 | GCTGTGATGATTGGC[A/C/G]TGCTTTCTGGAGCTG | 4666 |
rs144912354 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NACA | GRCh38.p7 | 12:56714276 | TAACCAAAATACCAC[A/C]TGTTCCCCAAAAACC | 4666 |
rs145075252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715778 | AGATTCACTGGAGAA[A/G]GCGGCGCATCACAGG | 4666 |
rs145187755 | snp | A/G | 0.00944217 | 0.0680583 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724536 | TTTCTGAAGGAAGGG[A/G]ATAAAAAGGAGGCCT | 4666 |
rs145337327 | snp | G/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720321 | AGATAATGAAAAAGA[G/T]GTAGCTACATTTAAG | 4666 |
rs145630440 | snp | A/T | 0.000511302 | 0.0159809 | synonymous-codon | NACA | GRCh38.p7 | 12:56713555 | GGCTTCCCCAAAAAC[A/T]ATGTAAGTATCTGAA | 4666 |
rs145648145 | snp | C/G | 0.000470651 | 0.0153331 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716118 | AGTGGGAACTGGGGA[C/G]GGAGCAAGAGGCAGA | 4666 |
rs145715716 | snp | C/G/T | 0.0190236 | 0.0959493 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727547 | ATAGTGCTAGGATTA[C/G/T]AGGTGTGAGCCACCA | 4666 |
rs146268086 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727938 | ATATATACACACACA[C/G]ACTCACACTCTAATT | 4666 |
rs146363625 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725958 | CCCCCAAAAAAAACA[C/T]TTCTTGTAACCAAAT | 4666 |
rs146755279 | snp | C/G | 0.000153988 | 0.00877328 | missense | NACA | GRCh38.p7 | 12:56713079 | CTTCCTCTTCACTCT[C/G]CTCTTGTACAGTTGG | 4666 |
rs146807178 | snp | A/G | 3.32541e-05 | 0.00407749 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720807 | GACTTGAGGGGAAGC[A/G]ATGGCTAGGGTAGTT | 4666 |
rs146850309 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NACA | GRCh38.p7 | 12:56723778 | GAACTTTTCATTACC[C/T]CCTCCTAAGTTTTCT | 4666 |
rs147175626 | snp | C/T | 0.000190027 | 0.00974564 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719118 | TGGAGGTCTTTTAGT[C/T]TGAGGAGACACACTA | 4666 |
rs147198460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56722237 | CTGTAATAGTCTCTA[C/T]AAACCTTCCTAGGTG | 4666 |
rs147776312 | snp | A/C/T | 6.65174e-05 | 0.00576671 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720035 | GTATCCTCAGAGTGG[A/C/T]TGCTACTTGAGTAGA | 4666 |
rs147964444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56714813 | GTTAAATGTAAACCA[A/T]CTGGCTTGTGTGAAG | 4666 |
rs148087516 | snp | A/G | 0.00111656 | 0.0236016 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721058 | AAGGAGGTGAAGTAA[A/G]AAGGTTAGGTGGAAA | 4666 |
rs148340957 | snp | C/T | 0.00112002 | 0.023638 | synonymous-codon | NACA | GRCh38.p7 | 12:56714677 | ATCACTGTCAGATTC[C/T]GTTCCAGACCCTAAG | 4666 |
rs148415721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56722895 | AATGTTAAGGGGGGC[A/G]GGGGGGAAGCCCGTG | 4666 |
rs148468202 | snp | C/G | 0.000307145 | 0.0123886 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718898 | TGGGGGGTAGTGTTA[C/G]TCCTTTGGGAGACAG | 4666 |
rs149157801 | snp | C/T | 3.2969e-05 | 0.00405998 | synonymous-codon | NACA | GRCh38.p7 | 12:56714428 | TTCATCAATTTCAGC[C/T]GCTGCCGCCAGCTAA | 4666 |
rs149200196 | snp | C/T | 0.0169215 | 0.0904124 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720329 | AAAAAGAGGTAGCTA[C/T]ATTTAAGGAGCCAGA | 4666 |
rs149326268 | snp | C/T | 0.00018425 | 0.00959641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716195 | TAGGAAGGACCTTCT[C/T]AAAGGCAGCTGCTGT | 4666 |
rs149732816 | snp | C/T | 3.29478e-05 | 0.00405867 | missense | NACA | GRCh38.p7 | 12:56712905 | CTACACCTGTTTCAT[C/T]GACCTGAGAGATGAG | 4666 |
rs149762980 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727410 | CGCGATCTCAGCTTA[C/T]TGCAACCTCCACCTC | 4666 |
rs149829623 | in-del | -/T | 0.0955749 | 0.196603 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728240 | CCAAGGAAGGATGTA[-/T]TTTTTTTTCCTTTTT | 4666 |
rs149905281 | snp | A/T | 0.0322114 | 0.122752 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712203 | TCGTGATCTGCCCCC[A/T]CCTTGGCCTCCCAAA | 4666 |
rs150062953 | snp | C/G | 0.00197699 | 0.0313781 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720277 | TAAGTGGCATTAGGA[C/G]AGCTTTTGAGAATGA | 4666 |
rs150387368 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56721976 | GTTAGTGAGCAGTGA[C/T]GATGATGGGGAATCT | 4666 |
rs150699625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56723096 | CATGGAATATGTTTT[C/G]TTCTGACTGGACCTC | 4666 |
rs150721914 | in-del | -/A | 0.00217335 | 0.032893 | intron-variant | NACA | GRCh38.p7 | 12:56715849 | AGACACACCATGCAC[-/A]ACGGCAAACCAAGGC | 4666 |
rs150775585 | snp | A/G | 0.0182019 | 0.0936463 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712116 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 4666 |
rs151092924 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | NACA | GRCh38.p7 | 12:56715398 | AAACAGATTTCTACA[A/T]TTTTATGAAAAGGGA | 4666 |
rs180713766 | snp | C/G | 0.00478085 | 0.0486577 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56711994 | CTTGCTCTGTCTGTC[C/G]CCCAGGCTGGAGTGC | 4666 |
rs180753340 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724215 | GCTTCTTTTGAGGCG[A/G]CAGGCATAACATAGA | 4666 |
rs181034081 | snp | G/T | 0.000316427 | 0.0125743 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720343 | ACATTTAAGGAGCCA[G/T]AAGGGCTGCAGGTTA | 4666 |
rs181212055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714078 | TCTTGAACTCCTGAC[C/T]TCAAGTGATCCATCT | 4666 |
rs181273401 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NACA | GRCh38.p7 | 12:56723739 | TAACGCTGCACAACT[A/G]ACTCAGAAAGGCTAT | 4666 |
rs181419853 | snp | G/T | 0.00317354 | 0.0397077 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719783 | CTTCAGGAGAAAGAG[G/T]TATCTCTGGAGAAGA | 4666 |
rs182115773 | snp | A/G | 0.00168813 | 0.0290037 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712598 | TTATAGGCAAATCAG[A/G]AGAATTCAGGTCACT | 4666 |
rs182130007 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726566 | ACAGGCGTGAGCCAC[C/T]ATGCCCAGCCTGTTT | 4666 |
rs182461681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715657 | AAAAATGATACACAA[G/T]GTACTATGTATCTAT | 4666 |
rs182949075 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721388 | GGGCAGGAGAGCAAG[A/G]AGGGGGGAGGGTAGG | 4666 |
rs183030473 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56721495 | ATAAAGAAAGGGGGA[A/G]GGGGAGGAGAAAAAA | 4666 |
rs183041989 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726306 | TTTTTTTTTTTTTTG[A/G]GTCGCTCTGTCGGCC | 4666 |
rs183171402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724818 | CCCCCTCCACTCCTA[A/C]TACTCACACTGGCTG | 4666 |
rs183828032 | snp | A/G | 0.00508699 | 0.0501759 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716216 | CAGCTGCTGTTAGAG[A/G]GGTGGACGCCTTAGA | 4666 |
rs183910000 | snp | A/G | 0.000633957 | 0.0177926 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720638 | TGGGAAAATCTGGGG[A/G]GGTGTTGGGACCCGC | 4666 |
rs184221111 | snp | C/T | 0.000153345 | 0.00875494 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716717 | GGGAAGGAGAAGTCA[C/T]AGCTGGTGGAATGAG | 4666 |
rs184283812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722728 | GACAATTGGAGTGGC[A/G]AGAATACACTGGATC | 4666 |
rs184509518 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726870 | CTACCGCCCCTGGCA[A/C]TTCTTGGATATTCTA | 4666 |
rs184762427 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56722423 | AGCCTGTAACAGTGG[A/C]TCATGCCTGTAATCC | 4666 |
rs185306381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56714186 | TACCACTACTAAGAA[C/T]TGGGTTCAGTGTATA | 4666 |
rs185499344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718929 | AGGAGTCACAGCTGA[A/G]GGAGTAGGGGCCCCT | 4666 |
rs185561121 | snp | A/G | 0.00235864 | 0.0342602 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719975 | CCAATACTGAACTGG[A/G]GAGATTTTTGAGGTC | 4666 |
rs185766417 | snp | A/G | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712278 | TCTTAAAAGAGGTAT[A/G]AAGTCTGAGATTCTA | 4666 |
rs185924864 | snp | A/G | 0.000116841 | 0.00764244 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720373 | ATGCTAGAGATGGTA[A/G]AGGGACCTTTGTCAA | 4666 |
rs186078027 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725906 | CTCATGCGTGTTAAA[C/G]TCTTCGTAAAACAAT | 4666 |
rs186314523 | snp | A/T | 1.66275e-05 | 0.00288331 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720793 | ATGGTGGTATCTTTG[A/T]CTTGAGGGGAAGCGA | 4666 |
rs186324721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723754 | GACTCAGAAAGGCTA[A/T]CATTTTAAGAACTTT | 4666 |
rs186519167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724378 | TAAAAAGTGTATTTC[C/T]CCTTGGTCATTTTGC | 4666 |
rs186711868 | snp | A/C | 0.000230639 | 0.0107362 | intron-variant | NACA | GRCh38.p7 | 12:56712914 | TTTCATCGACCTGAG[A/C]GATGAGAGGGAAAAA | 4666 |
rs187055425 | snp | A/G/T | 0.00176155 | 0.029626 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717001 | TCTTTGGGGGAAGAA[A/G/T]GAATCACAGCTGGCA | 4666 |
rs187293857 | snp | A/C/G/T | 0.00213889 | 0.0326381 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721391 | CAGGAGAGCAAGGAG[A/C/G/T]GGGGAGGGTAGGTCC | 4666 |
rs187514929 | snp | A/G | 0.000467337 | 0.0152791 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716239 | GCCTTAGACTCAGGA[A/G]GAGCCAAGGGGCCCT | 4666 |
rs187602721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56722097 | GGTGCACAGCACAAT[C/T]CAGTTCTTCCTAAAG | 4666 |
rs187896788 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726697 | CCTGCCTCAGCCTCC[C/T]GGGTAGCTGGGATTA | 4666 |
rs188125845 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726406 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 4666 |
rs188398122 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727505 | TCGAACTCCTGAGCT[A/C]AGGCAATCCACCCGC | 4666 |
rs188464432 | snp | C/T | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720145 | ATTGGAGGAGAAACA[C/T]AAGTAGCTACCTCAA | 4666 |
rs188713355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723086 | GAATTAAAAACATGG[A/T]ATATGTTTTCTTCTG | 4666 |
rs189174505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56715697 | TGAAAACCAAGATTT[A/G]GTTTCATATTCCTAG | 4666 |
rs189220434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56722437 | GCTCATGCCTGTAAT[C/T]CCAGCACTTCGGGAT | 4666 |
rs189221411 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56724069 | AACTAAAACCTTGAT[G/T]CAACTTGCTGGCTGG | 4666 |
rs189777655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714294 | TTCCCCAAAAACCTA[C/T]GGAAATAAACAGTTC | 4666 |
rs190289763 | snp | A/C/G | 0.00025727 | 0.011339 | intron-variant | NACA | GRCh38.p7 | 12:56713209 | CAGGGTAGAAAATAC[A/C/G]GATCCATGTGAGTAG | 4666 |
rs190291607 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712408 | TGGGGGGGTGGCGGG[A/G]AAGAGACCAGTCACC | 4666 |
rs190712969 | snp | A/C/T | 3.34265e-05 | 0.00408807 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721235 | GTAGGAAGGTTGGGG[A/C/T]TTCAGGGGCAGTTCC | 4666 |
rs190962151 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NACA | GRCh38.p7 | 12:56724804 | GACGCTACTGTGAAC[A/C]CCCTCCACTCCTAAT | 4666 |
rs191529968 | snp | G/T | 0.00408126 | 0.0449886 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717673 | ACTGCGGGATTGGGG[G/T]CCCCTTTGTGGGGTG | 4666 |
rs191637456 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726007 | CCTTGTATGGATAAC[G/T]TAATCCAGCTAAAAA | 4666 |
rs191919098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715769 | AACCCAAGCAGATTC[A/G]CTGGAGAAAGCGGCG | 4666 |
rs191979856 | snp | C/T | 3.32602e-05 | 0.00407786 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716384 | AGGGATCTGGGCATA[C/T]AGGAGGTGAAGTAGC | 4666 |
rs192219297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722461 | TCGGGATGCCTGGGA[G/T]GGCGGATCACGAGGT | 4666 |
rs192407324 | snp | G/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726450 | CCCCCGGCTAATTTT[G/T]TATTTTTAGTAGAGA | 4666 |
rs192460652 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726699 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA | 4666 |
rs192511809 | snp | A/C/G | 0.000903439 | 0.0212368 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720634 | GAAATGGGAAAATCT[A/C/G]GGGGGGTGTTGGGAC | 4666 |
rs192557798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56722164 | TCACTTAGCTTCTTT[A/G]TACCTTACCAGTTTA | 4666 |
rs192673445 | snp | C/G | 0.000362184 | 0.0134522 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721412 | GGGTAGGTCCAGGCT[C/G]CCCTAAGGCAGCAGT | 4666 |
rs193035118 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727728 | GGAAATTCTGAAATC[A/C]TCCTCAAATAGGAGA | 4666 |
rs199520749 | snp | A/G | 0.00276744 | 0.0370953 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718564 | GGAGGAGTTGCAGCT[A/G]GGGGTGTGGGGGCCC | 4666 |
rs199531072 | snp | A/G | 0.0535932 | 0.154675 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717709 | GCTAGACCTCCTTTT[A/G]GGGAGGGAGGAGTTG | 4666 |
rs199568239 | snp | A/G | 0.00582026 | 0.0536307 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718658 | GGGCCCATTTCGGGG[A/G]TGGGGTAGCTGGGCC | 4666 |
rs199597361 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726280 | CTATTTTGGGCACTT[C/T]TTGGATTTTTTTTTT | 4666 |
rs199681422 | snp | C/G | 0.00482958 | 0.0489026 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717023 | CAGCTGGCAGAGTGG[C/G]GGCCCCCATGGGGGC | 4666 |
rs199685932 | snp | C/T | 0.000499683 | 0.0157985 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720534 | CTTCACTGTAGGGTC[C/T]GACAAAGCACTAGGA | 4666 |
rs199686168 | snp | C/T | | | missense | NACA | GRCh38.p7 | 12:56714376 | CCTTCCGTGCCTTCT[C/T]TTCACTCCGACTCTG | 4666 |
rs199689133 | snp | A/G | 0.000224865 | 0.010601 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718964 | GGGATGGAGGAGTGG[A/G]AGAATGCGTCGTGGC | 4666 |
rs199720717 | snp | A/G | 0.000283326 | 0.0118989 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719562 | TGTGGGAGCCACCCC[A/G]GCAGGGTCAGCACTT | 4666 |
rs199723539 | snp | G/T | 5.05029e-05 | 0.00502483 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716151 | GACTGGTGGGGAGGG[G/T]GCTGCAGAGACAGAT | 4666 |
rs199756557 | snp | A/C | 0.000332541 | 0.0128903 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720025 | GGAGAGACTGGTATC[A/C]TCAGAGTGGTTGCTA | 4666 |
rs199883877 | snp | A/C | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712054 | CTGCCTCCCAGGTTC[A/C]CACCATTCTCCTGCC | 4666 |
rs199890485 | snp | C/G | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720129 | TATGGGACCTGATGA[C/G]ATTGGAGGAGAAACA | 4666 |
rs200033251 | snp | A/G | 0.000515047 | 0.0160393 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716661 | TGGGCCCTTTTCGGG[A/G]GATGGAGGAGTCACA | 4666 |
rs200069809 | snp | C/T | 1.66499e-05 | 0.00288525 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719606 | CAGCCACTGTTGGGG[C/T]AATGAGAGAACTTTT | 4666 |
rs200070725 | snp | G/T | 0.128632 | 0.218563 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717803 | GAGTTGCAGCTGGGG[G/T]TGTGGGGGCCCCTTT | 4666 |
rs200078093 | snp | A/T | 0.000296531 | 0.0121728 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712741 | AAAGTCACTCATAAT[A/T]GGTCAGGGCAGAGGG | 4666 |
rs200104799 | snp | A/G | 0.00134591 | 0.0259064 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720804 | TTTGACTTGAGGGGA[A/G]GCGATGGCTAGGGTA | 4666 |
rs200124165 | snp | A/G | 0.000527218 | 0.0162275 | intron-variant | NACA | GRCh38.p7 | 12:56713029 | ACAATGCTATACGGC[A/G]AGAGTTAAATTATGA | 4666 |
rs200125059 | snp | A/G | 0.0266355 | 0.112287 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717766 | GGGGGTGGGGTAGCT[A/G]GGCCTCCTTTTGGGG | 4666 |
rs200157165 | in-del | -/GAAG | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718337 | CTCCTTTTGGGGAGG[-/GAAG]AGTTGCAGCTGGGGT | 4666 |
rs200279695 | snp | C/G | 1.67298e-05 | 0.00289217 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721144 | GAAGAGGAAGGGGTC[C/G]CTTTCAGAGTTGGAG | 4666 |
rs200342422 | snp | C/G | 0.00545734 | 0.0519508 | intron-variant | NACA | GRCh38.p7 | 12:56714579 | TTCTTTGACCCAATA[C/G]CAGTTAGTAAGAGAA | 4666 |
rs200360816 | snp | A/G | 0.00147558 | 0.0271222 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718617 | ACCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs200363394 | snp | A/G | 0.00171941 | 0.0292703 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717445 | TCTTTGGAGGATGGA[A/G]TAGTTGGGCCTCCTT | 4666 |
rs200383188 | snp | A/C | 0.000176027 | 0.0093799 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718341 | TTTTGGGGAGGGAAG[A/C]GTTGCAGCTGGGGTT | 4666 |
rs200404679 | snp | A/G | 0.000482108 | 0.0155184 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720134 | GACCTGATGACATTG[A/G]AGGAGAAACACAAGT | 4666 |
rs200437576 | snp | A/G | 0.000164823 | 0.00907659 | missense | NACA | GRCh38.p7 | 12:56713575 | AAGTATCTGAAGCAG[A/G]GCTCTTGTAGACATC | 4666 |
rs200522112 | snp | C/T | 1.66391e-05 | 0.00288431 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719909 | GAGAGAAAGGGGCTC[C/T]TTCAAGAGAGGCAGG | 4666 |
rs200567357 | snp | A/G | 0.0266355 | 0.112287 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717755 | GGGCCCCTTTGGGGG[A/G]TGGGGTAGCTGGGCC | 4666 |
rs200603549 | in-del | -/TGGGCT | | | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717558 | GGGGGGTGGGGTACC[-/TGGGCT]TCCTTTTGGGGAGGG | 4666 |
rs200634986 | snp | C/T | 0.00199792 | 0.0315431 | missense | NACA | GRCh38.p7 | 12:56713628 | ATATTCTTAGATTTC[C/T]GGATAGTGACTCTAG | 4666 |
rs200685659 | snp | C/G | 0.00092361 | 0.0214698 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718951 | GGGGCCCCTTTGGGG[C/G]ATGGAGGAGTGGGAG | 4666 |
rs200740854 | snp | C/T | 4.98815e-05 | 0.00499382 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720779 | TCAGAACTGAGGAAA[C/T]GGTGGTATCTTTGAC | 4666 |
rs200794039 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56716119 | GTGGGAACTGGGGAG[A/G]GAGCAAGAGGCAGAG | 4666 |
rs200816397 | snp | G/T | 0.191743 | 0.243118 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719925 | TTCAAGAGAGGCAGG[G/T]ACAGTTTGGAGGTCT | 4666 |
rs200863350 | snp | A/G | 8.41361e-05 | 0.00648544 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717405 | TCCTTTGTGGGAGGG[A/G]GTTGCAGCTGGGGGA | 4666 |
rs200929777 | snp | A/G | 0.0188196 | 0.095161 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717768 | GGGTGGGGTAGCTGG[A/G]CCTCCTTTTGGGGAG | 4666 |
rs200942655 | snp | C/G | 0.000249644 | 0.0111696 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719768 | TCTTTGCTAGGGTGG[C/G]TTCAGGAGAAAGAGG | 4666 |
rs200948506 | snp | A/G | 0.00199809 | 0.0315444 | synonymous-codon | NACA | GRCh38.p7 | 12:56713176 | TAGTTGTGCTTGCTG[A/G]GATAAATCTTCGATC | 4666 |
rs200989071 | snp | C/G | 1.97136e-05 | 0.00313949 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717294 | TGCTGGAGCCTTTTT[C/G]GGGGAGAGAGGAATC | 4666 |
rs201015074 | snp | A/G/T | 3.40219e-05 | 0.00412432 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716580 | AGCTGGGGAAGTAGG[A/G/T]GAGTCTTTGAGGGAG | 4666 |
rs201104250 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728250 | ATGTATTTTTTTTTC[C/T]TTTTTTTTTTTTGAG | 4666 |
rs201182580 | snp | C/T | 4.95021e-05 | 0.0049748 | intron-variant | NACA | GRCh38.p7 | 12:56712957 | AGGCAAGAACAATTT[C/T]AGCAGTTCTTTGGAG | 4666 |
rs201249962 | snp | A/T | 0.128632 | 0.218563 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717804 | AGTTGCAGCTGGGGT[A/T]GTGGGGGCCCCTTTG | 4666 |
rs201259322 | snp | A/G/T | 0.000947379 | 0.021744 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720911 | CAGTACTGACTATAC[A/G/T]TGGAGGGCTGGGGGT | 4666 |
rs201261189 | snp | A/G | 5.15194e-05 | 0.00507514 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716022 | CAGCAGCTCATCCTC[A/G]TCAGCAGGGGCAAGG | 4666 |
rs201264467 | snp | A/G | 1.73694e-05 | 0.00294693 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721339 | GAAGGGAATGGGGAA[A/G]CCTGGTTAGCAGCTG | 4666 |
rs201268044 | in-del | -/CAAA | | | intron-variant | NACA | GRCh38.p7 | 12:56721632 | AACAACAACCTTCCC[-/CAAA]CATTTTTCAGTGGTC | 4666 |
rs201289550 | in-del | -/AC | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727929 | TCTGTGTGTATATAT[-/AC]ACACACACACTCACA | 4666 |
rs201290970 | snp | C/T | 1.66288e-05 | 0.00288343 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720086 | GTGCCATAACCAAGG[C/T]AGCAGGGGAAGTTGG | 4666 |
rs201354137 | snp | A/G/T | 0.000272306 | 0.0116657 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718405 | GGACTTCCTTTGGGG[A/G/T]AGGGAGGAGTTGCAG | 4666 |
rs201368647 | snp | A/G | 4.9826e-05 | 0.00499104 | intron-variant | NACA | GRCh38.p7 | 12:56713523 | GGAACAATGCCCAAG[A/G]AAAGTTTACTCACCT | 4666 |
rs201396601 | snp | A/G | 3.6224e-05 | 0.00425567 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718888 | GGGGTCTCTTTGGGG[A/G]GTAGTGTTACTCCTT | 4666 |
rs201446430 | snp | C/T | 1.66322e-05 | 0.00288371 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716357 | GGGGTCCTTTAGAAC[C/T]ATTCTTAGCTGAGGG | 4666 |
rs201572567 | snp | A/G/T | 0.0109877 | 0.0733027 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718654 | GTGGGGGCCCATTTC[A/G/T]GGGATGGGGTAGCTG | 4666 |
rs201610743 | snp | A/G | 1.7235e-05 | 0.00293551 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719049 | TTCAACTGGAGAAAC[A/G]GGGGATGAGAGATTT | 4666 |
rs201741745 | in-del | -/G | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717712 | GACCTCCTTTTAGGG[-/G]AGGGAGGAGTTGCAG | 4666 |
rs201766056 | snp | C/T | 0.00243126 | 0.034781 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717765 | GGGGGGTGGGGTAGC[C/T]GGGCCTCCTTTTGGG | 4666 |
rs201774060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713522 | TGGAACAATGCCCAA[G/T]AAAAGTTTACTCACC | 4666 |
rs201802620 | snp | G/T | 0.000133656 | 0.00817376 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721212 | GATGGGAGGCCCTAT[G/T]AGGTTTGGTAGGAAG | 4666 |
rs201846289 | snp | C/G | 1.66454e-05 | 0.00288486 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720718 | AAGGCAGCAGGTGGA[C/G]TAACAGGCCCCTTCA | 4666 |
rs201859253 | snp | C/G | 0.00399197 | 0.0444977 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718335 | ACCTCCTTTTGGGGA[C/G]GGAAGAGTTGCAGCT | 4666 |
rs201864281 | snp | C/T | 6.65115e-05 | 0.0057664 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720116 | GTTCTATGTTACTTA[C/T]GGGACCTGATGACAT | 4666 |
rs201868752 | snp | C/T | 0.000992334 | 0.0222527 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717446 | CTTTGGAGGATGGAG[C/T]AGTTGGGCCTCCTTT | 4666 |
rs201900348 | snp | C/T | 0.000436718 | 0.0147705 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720419 | CTGGAAAGGCAGCCA[C/T]AGTAGCAGGAACTAC | 4666 |
rs201913609 | snp | A/C | 0.00103585 | 0.0227344 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721105 | ACTGAGTGGGGAGCC[A/C]GGGCAACCAGAGCTA | 4666 |
rs201949086 | snp | A/G | 0.00399198 | 0.0444978 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717778 | GCTGGGCCTCCTTTT[A/G]GGGAGGGAGGAGTTG | 4666 |
rs201981844 | snp | C/T | 4.99397e-05 | 0.00499673 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719620 | GTAATGAGAGAACTT[C/T]TGAGAAGCGGACCAG | 4666 |
rs202018251 | snp | C/T | 0.00152867 | 0.0276043 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720908 | GAACAGTACTGACTA[C/T]ACATGGAGGGCTGGG | 4666 |
rs202022710 | snp | C/T | 3.33372e-05 | 0.00408258 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719931 | AGAGGCAGGTACAGT[C/T]TGGAGGTCTTTTTGT | 4666 |
rs202101850 | snp | C/T | 0.00199799 | 0.0315436 | intron-variant | NACA | GRCh38.p7 | 12:56713214 | TAGAAAATACAGATC[C/T]ATGTGAGTAGATTAG | 4666 |
rs202147060 | snp | A/C | 7.86102e-05 | 0.00626888 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717838 | GATGGGGTAGCCAGA[A/C]CTCCTTTTGGGGAGG | 4666 |
rs202147902 | snp | A/G | 0.000697757 | 0.0186653 | intron-variant | NACA | GRCh38.p7 | 12:56713010 | ATAGCTCACCAACAC[A/G]AACACAATGCTATAC | 4666 |
rs202197847 | snp | A/T | 1.65012e-05 | 0.00287234 | intron-variant | NACA | GRCh38.p7 | 12:56714450 | GCCAGCTAAGAAGAT[A/T]AAACAGCTATTAGTT | 4666 |
rs202204935 | snp | C/G | 1.96996e-05 | 0.00313838 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716793 | TGCTGGGGGACTGGA[C/G]GCCTCTTTGGAGGAT | 4666 |
rs367779814 | snp | C/G | 0.000267964 | 0.0115719 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717938 | GAGGAGTTGCAGCTG[C/G]GGTTGTGGGGGCCCC | 4666 |
rs367875595 | snp | G/T | 0.000297722 | 0.0121972 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721448 | TCAAGGCTGAAGACA[G/T]AGGTAGCACAGCTGG | 4666 |
rs367981476 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725442 | TTCCCACGGCGGGGG[G/T]GGTGACAAGGACTAA | 4666 |
rs368190606 | snp | A/C | 0.00398564 | 0.0444627 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712317 | ATCTGTGGCACTAAA[A/C]CTTATCAAATGAGGG | 4666 |
rs368249172 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56713333 | CACAGTAGAAAGAGT[A/G]GTTGTTTAGGTTTAG | 4666 |
rs368371411 | snp | C/T | 1.90652e-05 | 0.00308743 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717189 | GGGGGCTGAAGTTGC[C/T]GGGGCCTTTTTGAGG | 4666 |
rs368385711 | snp | A/G | 3.96865e-05 | 0.0044544 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717721 | TTTAGGGAGGGAGGA[A/G]TTGCAGCTGGGGGAG | 4666 |
rs368635646 | snp | C/T | 0.000346155 | 0.0131513 | intron-variant | NACA | GRCh38.p7 | 12:56712951 | AATTAAAGGCAAGAA[C/T]AATTTCAGCAGTTCT | 4666 |
rs368778367 | snp | A/G | 4.18218e-05 | 0.00457265 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717783 | GCCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs368887203 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719443 | ACCAAGGGTAAAGTA[G/T]TAAGAGTACCTTCCT | 4666 |
rs368947398 | snp | A/G | 5.01433e-05 | 0.00500691 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716224 | GTTAGAGGGGTGGAC[A/G]CCTTAGACTCAGGAG | 4666 |
rs368954017 | snp | G/T | 0.000193981 | 0.00984647 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720844 | GTTGTCTGAGGAAGG[G/T]AGGCCACTCCAGATT | 4666 |
rs369043787 | snp | A/G | 0.000897696 | 0.021167 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716431 | TGTGGACCTTTCCGA[A/G]TGGGAGCTGTGATGA | 4666 |
rs369112398 | snp | C/G | 0.000395922 | 0.0140643 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717472 | CCTTTAGAGGAGGGA[C/G]TTGTAGCTGGGAGAG | 4666 |
rs369140518 | snp | C/T | 1.72877e-05 | 0.00293999 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719137 | GGAGACACACTAACC[C/T]CTAAAGGAGATGGGG | 4666 |
rs369142123 | snp | A/G | 1.72484e-05 | 0.00293665 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719067 | GGATGAGAGATTTCC[A/G]ATAGGAGTATCAGGG | 4666 |
rs369162453 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725080 | GCCCCGCAGCCCTTC[C/T]ACCCTGCTTTTGCCA | 4666 |
rs369191826 | snp | A/G | 1.66515e-05 | 0.00288539 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719592 | TTCCAAAGGAAATGC[A/G]GCCACTGTTGGGGTA | 4666 |
rs369306783 | in-del | -/TCAG | | | intron-variant | NACA | GRCh38.p7 | 12:56713476 | ATCTGACGCAAAATG[-/TCAG]CAGTGCTGAGGTTGA | 4666 |
rs369375114 | snp | A/G | 5.89165e-05 | 0.00542723 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718320 | GGATGGGGTAGCTGG[A/G]CCTCCTTTTGGGGAG | 4666 |
rs369529375 | snp | A/C/T | 5.18536e-05 | 0.00509162 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716603 | TGAGGGAGGAAGGAG[A/C/T]CACAGGTGGGGAAGT | 4666 |
rs369553170 | snp | C/T | 1.87721e-05 | 0.00306361 | intron-variant | NACA | GRCh38.p7 | 12:56713218 | AAATACAGATCCATG[C/T]GAGTAGATTAGCAGT | 4666 |
rs369567341 | snp | A/G/T | 0.000326035 | 0.0127641 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718875 | CACTGAAGGAGTGGG[A/G/T]GTCTCTTTGGGGGGT | 4666 |
rs369587031 | snp | A/G | 0.000133047 | 0.00815512 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720943 | CCTTTTGGATTAGGG[A/G]CTACCTCAGAGGGAA | 4666 |
rs369596188 | snp | C/G/T | 0.000266564 | 0.011542 | intron-variant | NACA | GRCh38.p7 | 12:56714721 | TTTACTGCTTTATAG[C/G/T]AGAAATTATAAGAGA | 4666 |
rs369635295 | snp | A/C/G/T | 0.000354267 | 0.0133055 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717613 | GTGGGGGCCCCTTTG[A/C/G/T]GGGGTGAGGTAGCTG | 4666 |
rs369653107 | snp | A/G | 5.19251e-05 | 0.00509508 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718972 | GGAGTGGGAGAATGC[A/G]TCGTGGCTGGTGAGT | 4666 |
rs369666313 | snp | C/T | 3.69276e-05 | 0.00429679 | intron-variant | NACA | GRCh38.p7 | 12:56715831 | CAAGAGGGGTGTGGA[C/T]GACAGACACACCATG | 4666 |
rs369779499 | snp | C/T | 0.00052589 | 0.0162071 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718471 | GCTGCTGGACTTCCT[C/T]TGGGGGAGGGAGGAG | 4666 |
rs369832801 | snp | C/G | 3.33689e-05 | 0.00408453 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720364 | CTGCAGGTTATGCTA[C/G]AGATGGTAGAGGGAC | 4666 |
rs369977519 | snp | A/G | 0.000956151 | 0.021844 | intron-variant | NACA | GRCh38.p7 | 12:56724411 | ACCAAATGGCTTTAG[A/G]GTTAATTTTAATTAA | 4666 |
rs370114097 | snp | A/G | 9.94431e-05 | 0.00705065 | intron-variant | NACA | GRCh38.p7 | 12:56713703 | AGAAGAGAAAATAGT[A/G]TCAGGTTTTCAACCT | 4666 |
rs370136222 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56723134 | ATAAGCACTCAAATA[A/C]TTGCTTTGACACCAT | 4666 |
rs370183526 | snp | C/T | 3.30781e-05 | 0.00406669 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712586 | AATTAGCGGTTCTTA[C/T]AGGCAAATCAGGAGA | 4666 |
rs370262823 | snp | C/G | 0.000193981 | 0.00984647 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720391 | GGACCTTTGTCAACA[C/G]ATGGAGCCACCACTG | 4666 |
rs370285956 | snp | A/G | 0.000215224 | 0.0103714 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717663 | AGGAGTTACAACTGC[A/G]GGATTGGGGGCCCCT | 4666 |
rs370374927 | snp | C/G | 1.75984e-05 | 0.00296629 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719366 | CCAGCACTAAGGTAG[C/G]CAGAGGAGCACAGGT | 4666 |
rs370422156 | snp | A/G | 3.39345e-05 | 0.00411899 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719435 | CTGTAGGAACCAAGG[A/G]TAAAGTAGTAAGAGT | 4666 |
rs370481244 | snp | C/G | 0.00104745 | 0.0228611 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717686 | GGGCCCCTTTGTGGG[C/G]TGGGGTAGCTAGACC | 4666 |
rs370499042 | snp | G/T | 1.66291e-05 | 0.00288345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719988 | GGGGAGATTTTTGAG[G/T]TCTTCAGGGTCTGGC | 4666 |
rs370676194 | snp | C/T | 0.000282639 | 0.0118844 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720131 | TGGGACCTGATGACA[C/T]TGGAGGAGAAACACA | 4666 |
rs370841356 | snp | A/G | 0.000941003 | 0.0216706 | intron-variant | NACA | GRCh38.p7 | 12:56715829 | CCCAAGAGGGGTGTG[A/G]ACGACAGACACACCA | 4666 |
rs370891017 | snp | A/G | 0.000119306 | 0.0077226 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717732 | AGGAGTTGCAGCTGG[A/G]GGAGTGGGGGCCCCT | 4666 |
rs370916043 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722710 | ACAAAACAAACCAAA[A/G]AAGACAATTGGAGTG | 4666 |
rs370947040 | snp | A/T | 5.7814e-05 | 0.00537621 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717126 | AGGAGGAGTCACTGC[A/T]GGGAGGGTGGGATCC | 4666 |
rs370950923 | snp | A/G | 0.000123897 | 0.00786977 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721359 | GTTAGCAGCTGAGAG[A/G]GGGCACTGTTGTGGG | 4666 |
rs370964776 | snp | A/C/T | 3.32758e-05 | 0.00407885 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719908 | GGAGAGAAAGGGGCT[A/C/T]CTTCAAGAGAGGCAG | 4666 |
rs370984152 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56724896 | GGGAAAGACGGTGTT[G/T]TAAGTCCAACACTTG | 4666 |
rs371075827 | snp | C/T | 1.96493e-05 | 0.00313436 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717903 | GGGGGATGGGGTAGC[C/T]AGACCTCCTTTTGGG | 4666 |
rs371165343 | snp | C/G | 3.9152e-05 | 0.0044243 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718662 | CCATTTCGGGGATGG[C/G]GTAGCTGGGCCTCCT | 4666 |
rs371239609 | snp | A/G | 1.9477e-05 | 0.0031206 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716750 | GCTCTTTGGGGGATG[A/G]GGCCCCTTTGTAAGT | 4666 |
rs371261452 | snp | A/C | 4.95421e-05 | 0.00497681 | intron-variant | NACA | GRCh38.p7 | 12:56714702 | CCTAAGATGAGAAAC[A/C]ACTTTTACTGCTTTA | 4666 |
rs371282739 | snp | C/T | 3.33622e-05 | 0.00408412 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720677 | GAGAAGAGGTCACCA[C/T]AGGAAGAGACTGAGT | 4666 |
rs371375736 | snp | A/G | 7.73545e-05 | 0.00621862 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716735 | CTGGTGGAATGAGGA[A/G]CTCTTTGGGGGATGG | 4666 |
rs371470990 | snp | A/G | 0.000133041 | 0.00815491 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720304 | ATGAGAGAGGTTGTA[A/G]GAGATAATGAAAAAG | 4666 |
rs371523418 | snp | C/T | 8.31414e-05 | 0.006447 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720912 | AGTACTGACTATACA[C/T]GGAGGGCTGGGGGTG | 4666 |
rs371556274 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714109 | GCCTTGGCCTTCCAG[C/T]GTGCTGGGATAACAG | 4666 |
rs371585871 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725937 | GTTAGCTGTACCCCC[C/G]CCCCCCCCCCAAAAA | 4666 |
rs371618209 | snp | C/G | 0.00016995 | 0.00921663 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724544 | GGAAGGGAATAAAAA[C/G]GAGGCCTAAATTGAT | 4666 |
rs371710098 | snp | G/T | 0.000175956 | 0.009378 | intron-variant | NACA | GRCh38.p7 | 12:56721477 | GGAGAAAGGCAAAAG[G/T]AGATAAAGAAAGGGG | 4666 |
rs371952741 | snp | A/C | 0.000193981 | 0.00984647 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716165 | GTGCTGCAGAGACAG[A/C]TGCTGATTCAGGTTT | 4666 |
rs371978815 | snp | C/T | 0.00045027 | 0.0149977 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717950 | CTGGGGTTGTGGGGG[C/T]CCCTTTGGGGGATGG | 4666 |
rs372131023 | snp | A/G | 0.000209978 | 0.0102443 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718314 | CTTGAGGGATGGGGT[A/G]GCTGGACCTCCTTTT | 4666 |
rs372139516 | snp | A/T | 1.73954e-05 | 0.00294913 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718961 | TGGGGGATGGAGGAG[A/T]GGGAGAATGCGTCGT | 4666 |
rs372164873 | snp | A/C/G | 3.29561e-05 | 0.00405921 | intron-variant | NACA | GRCh38.p7 | 12:56713043 | CGAGAGTTAAATTAT[A/C/G]AAAGATTTCCTAGTA | 4666 |
rs372189050 | snp | G/T | 0.000116396 | 0.00762788 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720254 | TTTGGGCCACTAAAG[G/T]ATAATGATAAGTGGC | 4666 |
rs372259757 | snp | C/T | 0.000133012 | 0.00815403 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720863 | CCACTCCAGATTGAA[C/T]AGAGGCCATGGGAGT | 4666 |
rs372435791 | snp | A/G | 1.81757e-05 | 0.00301455 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718729 | GCCCCTTTGGGGGAT[A/G]GGGAAGCTGGGATTC | 4666 |
rs372484247 | snp | C/G | 0.000184003 | 0.00958999 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716209 | TCAAAGGCAGCTGCT[C/G]TTAGAGGGGTGGACG | 4666 |
rs372503104 | snp | A/T | 0.000522916 | 0.0161612 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717009 | GGAAGAAGGAATCAC[A/T]GCTGGCAGAGTGGGG | 4666 |
rs372550236 | snp | C/G | 1.66749e-05 | 0.00288741 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719507 | TTCCTTCTAGAAAAG[C/G]GCTGGCTGTAGTTGT | 4666 |
rs372575337 | snp | A/G/T | 1.6633e-05 | 0.00288378 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720955 | GGGACTACCTCAGAG[A/G/T]GAACTTTATTAAGAT | 4666 |
rs372593565 | snp | C/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719498 | AAGAGACAGTTCCTT[C/T]TAGAAAAGGGCTGGC | 4666 |
rs372656831 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726158 | AGATTCCGGCCCTTT[C/T]GATTGTTTTAGGTTC | 4666 |
rs372666259 | snp | A/G | 0.000192652 | 0.0098127 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717258 | GGATGGGGTGGCTGC[A/G]CCTTCTCTGGTGACT | 4666 |
rs372688513 | snp | A/G/T | 0.000586844 | 0.0171199 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718975 | GTGGGAGAATGCGTC[A/G/T]TGGCTGGTGAGTCTT | 4666 |
rs372706535 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722902 | AGGGGGGCGGGGGGG[A/G]AGCCCGTGGTACCAA | 4666 |
rs372794179 | snp | G/T | 1.66316e-05 | 0.00288367 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716445 | AGTGGGAGCTGTGAT[G/T]ATTGGCGTGCTTTCT | 4666 |
rs372797975 | snp | C/T | 5.02744e-05 | 0.00501345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721267 | AAAGGTAGGGCTGTT[C/T]CAGAGGATGACTGGG | 4666 |
rs372859301 | snp | C/G | 1.98065e-05 | 0.00314688 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717512 | CTTTAGGGGAGGGAG[C/G]AGTTACAGCTGGGGG | 4666 |
rs372870025 | snp | C/T | 3.29685e-05 | 0.00405995 | intron-variant | NACA | GRCh38.p7 | 12:56714559 | GTTGCCCTGATCAAC[C/T]CTGCTTCTTTGACCC | 4666 |
rs372899081 | snp | G/T | 3.52429e-05 | 0.00419764 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719215 | GCACCAGAGTCCTCA[G/T]TTGGGCACTCTTTGG | 4666 |
rs373017103 | snp | C/T | 3.33239e-05 | 0.00408177 | intron-variant | NACA | GRCh38.p7 | 12:56713515 | CCTGGTCTGGAACAA[C/T]GCCCAAGAAAAGTTT | 4666 |
rs373255556 | snp | C/G/T | 9.9826e-05 | 0.00706428 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719802 | CTCTGGAGAAGAGGA[C/G/T]GTACTTTGGAAAGAA | 4666 |
rs373296467 | snp | A/C | 0.000451154 | 0.0150124 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719280 | AGAAATACCATCAAC[A/C]TTTTTTGTACCTGGA | 4666 |
rs373370096 | snp | C/G | 0.000153988 | 0.00877328 | missense | NACA | GRCh38.p7 | 12:56713562 | CCAAAAACTATGTAA[C/G]TATCTGAAGCAGGGC | 4666 |
rs373475432 | snp | A/G | 0.000333128 | 0.0129017 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716770 | CCTTTGTAAGTGGAA[A/G]GAGTCACTGCTGGGG | 4666 |
rs373582016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719370 | CACTAAGGTAGCCAG[A/G]GGAGCACAGGTATTC | 4666 |
rs373860894 | snp | A/C | 0.00131309 | 0.0255895 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717631 | GGTGAGGTAGCTGGG[A/C]CTCCTTTTGGAGAGG | 4666 |
rs374046972 | snp | A/C | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712218 | TCCTTGGCCTCCCAA[A/C]GTGCCAGGATTACAG | 4666 |
rs374167103 | snp | A/C | 0.000106341 | 0.00729105 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718749 | AGCTGGGATTCCTTT[A/C]GGGGCTGGAGTTGCT | 4666 |
rs374168332 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716093 | GCAGAAATTGCTGTT[C/T]AGGAGGCAGAGTGGG | 4666 |
rs374318467 | snp | G/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714547 | CCAAATACAAAAGTT[G/T]CCCTGATCAACCCTG | 4666 |
rs374416918 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722713 | AAACAAACCAAAGAA[A/G]ACAATTGGAGTGGCG | 4666 |
rs374457680 | snp | A/G | 3.29636e-05 | 0.00405964 | intron-variant | NACA | GRCh38.p7 | 12:56714576 | TGCTTCTTTGACCCA[A/G]TACCAGTTAGTAAGA | 4666 |
rs374492724 | snp | C/T | 1.83427e-05 | 0.00302837 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715910 | GCTTGGCAGAGGGGG[C/T]TGGGACAGGGATTCC | 4666 |
rs374494657 | snp | C/G | 1.78816e-05 | 0.00299006 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719306 | CTGGAGGAGTCCCAG[C/G]TGGGGGAAGAGAGGG | 4666 |
rs374568695 | snp | C/G | 1.80159e-05 | 0.00300127 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721372 | AGAGGGCACTGTTGT[C/G]GGGCAGGAGAGCAAG | 4666 |
rs374589645 | snp | A/G | 0.00442542 | 0.0468308 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720690 | CACAGGAAGAGACTG[A/G]GTTGAAAGAGATAAG | 4666 |
rs374710825 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56724368 | CCCATCCTCCTAAAA[-/A]GTGTATTTCCCCTTG | 4666 |
rs374730583 | snp | C/T | 1.75302e-05 | 0.00296054 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718946 | GAGTAGGGGCCCCTT[C/T]GGGGGATGGAGGAGT | 4666 |
rs374758568 | snp | C/T | 4.95462e-05 | 0.00497701 | intron-variant | NACA | GRCh38.p7 | 12:56714340 | TGCTTCATAAGATCC[C/T]GAAATCCTTTTCAAA | 4666 |
rs374836466 | snp | A/C/G | 3.3315e-05 | 0.00408122 | intron-variant, missense, stop-gained | NACA | GRCh38.p7 | 12:56719579 | CAGGGTCAGCACTTT[A/C/G]CAAAGGAAATGCAGC | 4666 |
rs374933462 | snp | A/G | 0.000315953 | 0.0125649 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720310 | GAGGTTGTAGGAGAT[A/G]ATGAAAAAGAGGTAG | 4666 |
rs375012026 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716528 | GAAGCCCTTTAGATG[C/T]TTGAGGAACAGTGGC | 4666 |
rs375014973 | snp | A/G | 1.66441e-05 | 0.00288474 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719680 | TTGATTACAGAGGCC[A/G]AGGAGTTAACACCCA | 4666 |
rs375028867 | snp | A/C | 7.69468e-05 | 0.00620221 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717140 | CTGGGAGGGTGGGAT[A/C]CCCTTTGGAGGATGG | 4666 |
rs375039667 | snp | A/G | 0.000458657 | 0.0151367 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721306 | ACTTCTAAAGGGGTC[A/G]AGGCAATAGTAGAGG | 4666 |
rs375227623 | snp | A/G | 0.000520543 | 0.0161245 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724548 | GGGAATAAAAAGGAG[A/G]CCTAAATTGATTGGG | 4666 |
rs375269668 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724900 | AAGACGGTGTTTTAA[A/G]TCCAACACTTGCTTG | 4666 |
rs375312973 | snp | A/G | 0.000150679 | 0.00867853 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719464 | GTACCTTCCTTAACT[A/G]GGTGGTTTTTAGGAG | 4666 |
rs375346587 | snp | G/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724116 | CGGGCTCCTTGGCCT[G/T]TGTCATCTAGTTCCA | 4666 |
rs375354943 | snp | A/G | 0.000196831 | 0.00991851 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718293 | AGCTGGGGGAGTGGG[A/G]GCCCCCTTGAGGGAT | 4666 |
rs375441596 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726990 | GTGTTAATGAAAAGC[C/T]TCCCATATCTTCCCA | 4666 |
rs375518907 | snp | A/G/T | 0.00339757 | 0.0410766 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717734 | GAGTTGCAGCTGGGG[A/G/T]AGTGGGGGCCCCTTT | 4666 |
rs375567238 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56713297 | AGGTAACTTATTGTA[A/C]AGCTTTAAACTGCTT | 4666 |
rs375567633 | snp | A/G | 0.000116462 | 0.00763003 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720988 | GTCTTTGGTTCTGAG[A/G]GAGCAATGGGAGCTG | 4666 |
rs375605609 | snp | C/G | 0.000209582 | 0.0102346 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717212 | TTTTGAGGGAGACAG[C/G]AGTCACTGCTGGGGG | 4666 |
rs375771251 | snp | G/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727248 | CGTAGGTTATCCGCC[G/T]GCCTCAGCCTCCCAA | 4666 |
rs375774655 | snp | A/G | 1.66346e-05 | 0.00288393 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716323 | ACAGGGAGTAGAGGG[A/G]CTGGAGCCACTGTGG | 4666 |
rs375850373 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | NACA | GRCh38.p7 | 12:56714447 | GCCGCCAGCTAAGAA[A/G]ATAAAACAGCTATTA | 4666 |
rs375889518 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56723382 | TATTTGTAAAATTAA[-/A]GTTGTTCAATGACAC | 4666 |
rs375914904 | snp | C/T | 0.000230719 | 0.0107381 | intron-variant | NACA | GRCh38.p7 | 12:56713028 | CACAATGCTATACGG[C/T]GAGAGTTAAATTATG | 4666 |
rs376040666 | snp | A/G | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725070 | TTCTGGGCCCGCCCC[A/G]CAGCCCTTCTACCCT | 4666 |
rs376062595 | snp | C/T | 0.000266033 | 0.0115302 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719983 | GAACTGGGGAGATTT[C/T]TGAGGTCTTCAGGGT | 4666 |
rs376126387 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718085 | CAGCTGGGGTTGTGG[A/G]GGCCCCTTTTGGGGG | 4666 |
rs376136932 | snp | A/G | 0.000567819 | 0.01684 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719260 | GGTGCCAATGCTGAA[A/G]TATGAGAAATACCAT | 4666 |
rs376202677 | snp | A/G/T | 3.32001e-05 | 0.00407421 | intron-variant | NACA | GRCh38.p7 | 12:56713525 | AACAATGCCCAAGAA[A/G/T]AGTTTACTCACCTTG | 4666 |
rs376234480 | snp | A/G | 5.27551e-05 | 0.00513564 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56718766 | GGGCTGGAGTTGCTC[A/G]GGCCTTTTTGGGGGA | 4666 |
rs376361769 | snp | A/G | 0.000237949 | 0.0109049 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717547 | GGGGCCCCTTTGGGG[A/G]GTGGGGTACCTGGGC | 4666 |
rs376486851 | snp | A/C/G | 7.06182e-05 | 0.00594179 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719353 | GGGATTTCAGGGGCC[A/C/G]GCACTAAGGTAGCCA | 4666 |
rs376636991 | snp | A/G | 3.32557e-05 | 0.00407759 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720150 | AGGAGAAACACAAGT[A/G]GCTACCTCAAAGGTA | 4666 |
rs376681262 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56715299 | AACATAATTCACATA[A/C]ATTTCTTTCAATTCA | 4666 |
rs376706368 | snp | C/T | 0.000133505 | 0.00816912 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720651 | GGGGGTGTTGGGACC[C/T]GCAGTCTTTTGAGAA | 4666 |
rs376839820 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56724910 | TTAAGTCCAACACTT[-/A]GCTTGTCACAGGGAG | 4666 |
rs376889735 | snp | C/T | 0.000254844 | 0.0112853 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716870 | TAGGGGAGGGAACAG[C/T]CATAGCTGGGGGAAT | 4666 |
rs376895860 | snp | C/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715720 | ATTCCTAGAACTTTT[C/G]CATTTAAAATTATCA | 4666 |
rs376921753 | snp | G/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723979 | TAGGACGACTCTGGG[G/T]CCCAGTAGGACACAT | 4666 |
rs376972317 | snp | C/G/T | 0.000121559 | 0.00779527 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718971 | AGGAGTGGGAGAATG[C/G/T]GTCGTGGCTGGTGAG | 4666 |
rs377000958 | snp | A/G | 0.000397007 | 0.0140835 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719130 | AGTCTGAGGAGACAC[A/G]CTAACCCCTAAAGGA | 4666 |
rs377020953 | snp | C/T | 0.00064566 | 0.0179559 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717662 | GAGGAGTTACAACTG[C/T]GGGATTGGGGGCCCC | 4666 |
rs377059692 | in-del | -/AATTA | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727908 | TTGTTTGGAAGATTA[-/AATTA]GTCTGTGTGTATATA | 4666 |
rs377067997 | snp | A/G | 4.96093e-05 | 0.00498018 | intron-variant | NACA | GRCh38.p7 | 12:56713692 | ACATAGCCTAAAGAA[A/G]AGAAAATAGTATCAG | 4666 |
rs377200358 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725468 | ACTAAAGGGTAAGAA[C/T]TTAGAACGGGACGCG | 4666 |
rs377222121 | snp | A/C/G | 3.88986e-05 | 0.00441 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718407 | ACTTCCTTTGGGGGA[A/C/G]GGAGGAGTTGCAGCT | 4666 |
rs377222293 | snp | A/G | 0.000383311 | 0.0138387 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719523 | GCTGGCTGTAGTTGT[A/G]TAAGTTGAGGTACCT | 4666 |
rs377256223 | snp | C/T | 1.67823e-05 | 0.0028967 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721275 | GGCTGTTCCAGAGGA[C/T]GACTGGGGAAAAGGA | 4666 |
rs377282943 | snp | A/G | 1.72487e-05 | 0.00293667 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718992 | GGCTGGTGAGTCTTT[A/G]GAGCCTTGGAAAGAA | 4666 |
rs377340336 | snp | A/G | 1.67231e-05 | 0.00289159 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721117 | GCCAGGGCAACCAGA[A/G]CTAAGGGAGCTGAAG | 4666 |
rs377353603 | snp | G/T | 0.000215977 | 0.0103895 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718582 | GGTGTGGGGGCCCCT[G/T]TGGGGGATGGAGTAG | 4666 |
rs377411438 | snp | A/C | 1.95704e-05 | 0.00312807 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717675 | TGCGGGATTGGGGGC[A/C]CCTTTGTGGGGTGGG | 4666 |
rs377508251 | snp | A/C/T | 3.31204e-05 | 0.00406931 | intron-variant | NACA | GRCh38.p7 | 12:56714710 | GAGAAACAACTTTTA[A/C/T]TGCTTTATAGTAGAA | 4666 |
rs377573124 | snp | A/G | 1.66963e-05 | 0.00288927 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720377 | TAGAGATGGTAGAGG[A/G]ACCTTTGTCAACAGA | 4666 |
rs377576508 | snp | C/G/T | 9.06337e-05 | 0.00673124 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715992 | CCCAGAGATTGGTTC[C/G/T]GGGGGAATCAGAGGC | 4666 |
rs386763309 | multinucleotide-polymorphism | AA/GC | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728132 | GAAGGACCAGAAATA[AA/GC]CAATTTCCTTAGACA | 4666 |
rs397747302 | in-del | -/A | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725955 | CCCCCCCAAAAAAAA[-/A]CACTTCTTGTAACCA | 4666 |
rs527361962 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant | NACA | GRCh38.p7 | 12:56713049 | TTAAATTATGAAAGA[C/T]TTCCTAGTATACCTC | 4666 |
rs527469860 | snp | C/T | 3.93484e-05 | 0.00443539 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718300 | GGAGTGGGGGCCCCC[C/T]TGAGGGATGGGGTAG | 4666 |
rs527554681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717943 | GTTGCAGCTGGGGTT[A/G]TGGGGGCCCCTTTGG | 4666 |
rs527662321 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715711 | TGGTTTCATATTCCT[A/G]GAACTTTTGCATTTA | 4666 |
rs527671988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56713949 | CAGGTTCAAGCAATT[A/G]CCGTGCCTCAGCCAC | 4666 |
rs527698731 | snp | C/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712366 | ATAAATTACTAGAAC[C/G/T]TTTTTAAGTTTTTTT | 4666 |
rs527886025 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725100 | TGCTTTTGCCAGGAC[A/G]CCAACCGCAGACCCC | 4666 |
rs528063005 | snp | A/G | 5.93102e-05 | 0.00544533 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716836 | GCTTCTTTGGGGGTT[A/G]GAATTGCTGGGGTCT | 4666 |
rs528092400 | snp | C/T | 2.08002e-05 | 0.00322485 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717355 | GATGGGATAGCTGGT[C/T]CTCTTTTGGGGGAGG | 4666 |
rs528222000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722226 | CCACAAAAGGACTGT[A/C]ATAGTCTCTATAAAC | 4666 |
rs528243261 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727928 | GTCTGTGTGTATATA[C/T]ACACACACACACTCA | 4666 |
rs528636657 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56724335 | TTTACGGTCTATCCT[A/C]CTTGGTAAAGCTGCA | 4666 |
rs528876497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717854 | CTCCTTTTGGGGAGG[A/G]AGGAGTTGCAGCTGG | 4666 |
rs529258222 | snp | A/G | 0.000117541 | 0.00766529 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718339 | CCTTTTGGGGAGGGA[A/G]GAGTTGCAGCTGGGG | 4666 |
rs529654357 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727762 | AATATTGTGGAGTCA[A/T]TAAAGACAGACTCTG | 4666 |
rs529757206 | in-del | -/AA | 0.000653162 | 0.0180597 | intron-variant | NACA | GRCh38.p7 | 12:56714731 | TATAGTAGAAATTAT[-/AA]GAGAAGGTACTTCAC | 4666 |
rs529929746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724775 | GGGCTGGCTCTCGAT[A/C]ATGGGAGACTTCAGA | 4666 |
rs530299780 | snp | C/G | 0.000348966 | 0.0132046 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715885 | CCCTTGTTGTTCTTC[C/G]TAACAGGTTGCTTGG | 4666 |
rs530418404 | snp | A/G | 3.90503e-05 | 0.00441855 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721437 | AGCAGTGACACTCAA[A/G]GCTGAAGACATAGGT | 4666 |
rs530427863 | snp | C/G | 3.34124e-05 | 0.00408719 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716230 | GGGGTGGACGCCTTA[C/G]ACTCAGGAGGAGCCA | 4666 |
rs530534264 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56722133 | ACACTTCAGAATTTA[A/C]TATCAAGTATTAAAG | 4666 |
rs530750573 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728074 | CTAATAAATACATGA[G/T]CTGGAAGATTTTCAA | 4666 |
rs531018559 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727222 | CCCGCCTCCCCGCCC[A/G]GACTCCTGACCGTAG | 4666 |
rs531282060 | in-del | -/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724638 | AGAAAAAAATCGTGA[-/G]GGTGTTTGGTGACAA | 4666 |
rs531385852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713292 | CATTCAGGTAACTTA[C/T]TGTACAGCTTTAAAC | 4666 |
rs531721623 | snp | C/T | 0 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56715694 | TAATGAAAACCAAGA[C/T]TTGGTTTCATATTCC | 4666 |
rs531804861 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726569 | GGCGTGAGCCACCAT[A/G]CCCAGCCTGTTTGTT | 4666 |
rs531924947 | snp | C/T | 6.65779e-05 | 0.00576927 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719633 | TTTTGAGAAGCGGAC[C/T]AGCAGAGTCTGGGCC | 4666 |
rs531992839 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726667 | CAACCTCCCCTTCCC[A/G]GGTCAAGCGATTCTC | 4666 |
rs532026011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724847 | TGGGCTGGGGCCTCC[C/T]GGACTACGTTTGCCG | 4666 |
rs532122829 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727671 | TGAGGATTAGGATTG[A/G]TGAATTAAAATTAAG | 4666 |
rs532274743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713826 | AATGGGTTTTCTGCC[A/G]TAGTAACTTCTGTTA | 4666 |
rs532587307 | snp | A/G | 3.32546e-05 | 0.00407752 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720777 | AATCAGAACTGAGGA[A/G]ATGGTGGTATCTTTG | 4666 |
rs532682017 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56722225 | CCACAAAAGGACTGT[-/A]AATAGTCTCTATAAA | 4666 |
rs532693960 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727720 | CAGGAATGGGAAATT[C/T]TGAAATCCTCCTCAA | 4666 |
rs533140819 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56723698 | AAGGTGAGAATGAAA[A/T]TTACAGCCTGAAGAT | 4666 |
rs533157907 | snp | A/G | 1.96254e-05 | 0.00313246 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717904 | GGGGATGGGGTAGCT[A/G]GACCTCCTTTTGGGG | 4666 |
rs533529104 | snp | C/T | 5.93783e-05 | 0.00544845 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717569 | TACCTGGGCTTCCTT[C/T]TGGGGAGGGAGGAGT | 4666 |
rs533581193 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56724598 | CCGGAGATAAGTATT[A/C]TTAAAAACTCCGAGG | 4666 |
rs533790608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723937 | AAGTATCTCAGCACC[A/G]CCAACCCATAAACAA | 4666 |
rs534010030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713368 | GTGGTTCTCAACTAG[C/G]GGGTAGTTAGGTCTC | 4666 |
rs534390661 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718524 | CCCTTTGGGGGATGG[A/G]GTAGCTGGACCTCCT | 4666 |
rs534417377 | snp | A/G | 6.58957e-05 | 0.00573964 | synonymous-codon | NACA | GRCh38.p7 | 12:56712906 | TACACCTGTTTCATC[A/G]ACCTGAGAGATGAGA | 4666 |
rs534530232 | snp | A/G | 0.110519 | 0.207473 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718150 | GTTGCAGCTGGGGTT[A/G]TGGGTGCCCCTTTGT | 4666 |
rs534603104 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723670 | TAACAAATGAAATTT[A/T]AAAAAAACCAAAAAG | 4666 |
rs534688195 | snp | A/G/T | 3.32752e-05 | 0.00407881 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716312 | AGTCTTTCTGAACAG[A/G/T]GAGTAGAGGGGCTGG | 4666 |
rs534707813 | snp | A/C | 5.7833e-05 | 0.0053771 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717117 | CTTGGGGGAAGGAGG[A/C]GTCACTGCTGGGAGG | 4666 |
rs534833988 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723366 | TGAATTTCAAATCTT[C/T]GTATTTGTAAAATTA | 4666 |
rs535034188 | snp | A/G | 5.06248e-05 | 0.00503089 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720480 | AGATCTCTGAGAAGG[A/G]TAAGAGGCCCCTGTG | 4666 |
rs535202162 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56721992 | GATGATGGGGAATCT[A/G]AACTGAATAAGAAAA | 4666 |
rs535465765 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712059 | TCCCAGGTTCACACC[A/C]TTCTCCTGCCTCAGC | 4666 |
rs535607245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723776 | AAGAACTTTTCATTA[C/T]CTCCTCCTAAGTTTT | 4666 |
rs535779977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721668 | GTGAGAAGACATTCC[C/T]CTCCTAATTTCTCAC | 4666 |
rs535839261 | snp | A/G | 5.0058e-05 | 0.00500265 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720366 | GCAGGTTATGCTAGA[A/G]ATGGTAGAGGGACCT | 4666 |
rs535853757 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56722812 | TTTGGCATGACAGTA[A/C]GACAGTATCTCTGGC | 4666 |
rs535923910 | snp | A/G | 1.98758e-05 | 0.00315238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717893 | GGGCCCCTTTGGGGG[A/G]TGGGGTAGCTAGACC | 4666 |
rs536209208 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728199 | CAAGCCCACTTACTT[C/T]TTCCTCTCTCTGTAG | 4666 |
rs536263208 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720735 | AACAGGCCCCTTCAG[A/G]CTGAGGCTTCCTGGG | 4666 |
rs536380481 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726816 | TTCAGGTGATCCGCC[G/T]GCCTCGGCCTCCCAA | 4666 |
rs536402864 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725315 | ACCGAGCGAGAGCGT[A/G]ACCCACGCCTGTTGC | 4666 |
rs536645117 | snp | A/G | 1.66346e-05 | 0.00288393 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720963 | CTCAGAGGGAACTTT[A/G]TTAAGATTAGTCTTT | 4666 |
rs536800364 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727003 | GCCTCCCATATCTTC[C/T]CACAGCCCTACAAAA | 4666 |
rs536869655 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728205 | CACTTACTTTTTCCT[C/G]TCTCTGTAGTAATGA | 4666 |
rs536869747 | snp | A/C/G | 1.67528e-05 | 0.00289415 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720404 | CAGATGGAGCCACCA[A/C/G]TGGAAAGGCAGCCAC | 4666 |
rs536998099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721778 | GGAGCACAGACTCTT[C/G]GTAGGTTGAGAACAA | 4666 |
rs537391888 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726196 | TTTAGCCGATGTTGA[A/T]ATTATAAAGCTGCAG | 4666 |
rs537461198 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725236 | GGATGGCTGCGGATA[C/G]ACAGTAGCGGCACAG | 4666 |
rs537467637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722430 | AACAGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 4666 |
rs537859542 | snp | A/C/G | 7.87223e-05 | 0.00627345 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718644 | AGCTGGGGGTGTGGG[A/C/G]GCCCATTTCGGGGAT | 4666 |
rs538198092 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725880 | CAAACGATGTCACCA[C/G]ATGACAGCAACTCAT | 4666 |
rs538221242 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727065 | AGCTAAACCAGTCAA[C/T]ATTTATTTATTTTTT | 4666 |
rs538409774 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722113 | CAGTTCTTCCTAAAG[C/T]TGAAACACTTCAGAA | 4666 |
rs538432700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713465 | AACAGAGAACTATCT[A/G]ACGCAAAATGTCAGC | 4666 |
rs538444719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56714069 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAAGT | 4666 |
rs538677946 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723007 | GCTCAACTAGTTTTT[C/T]CTGGAGAGTGGGTAG | 4666 |
rs538991969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714153 | ACCTAGCTACTTCTG[C/T]TACTTTCAACGGGAT | 4666 |
rs539059889 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727403 | GCAGTGGCGCGATCT[C/G]AGCTTACTGCAACCT | 4666 |
rs539422172 | snp | C/T | 4.98948e-05 | 0.00499449 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716447 | TGGGAGCTGTGATGA[C/T]TGGCGTGCTTTCTGG | 4666 |
rs539575150 | snp | C/T | 3.89476e-05 | 0.00441274 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718389 | GAGTGGGGTAGCTGC[C/T]GGACTTCCTTTGGGG | 4666 |
rs539747122 | snp | A/G | 1.93463e-05 | 0.00311011 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717041 | CCCCCATGGGGGCTG[A/G]AGTTGCTGGGGCCTT | 4666 |
rs539783910 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACA | GRCh38.p7 | 12:56723103 | TATGTTTTCTTCTGA[C/T]TGGACCTCAAATGGA | 4666 |
rs539972834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723844 | CTTCACAGTCGTTAA[C/T]TTCGACGCTGAGGAT | 4666 |
rs540039504 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718095 | TGTGGGGGCCCCTTT[G/T]GGGGGTGGGGTAGCT | 4666 |
rs540194779 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACA | GRCh38.p7 | 12:56723461 | CAGTACTTTATTTTT[C/T]CCCTTCCTTAAGCCC | 4666 |
rs540373720 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56722665 | TGCATGCACTCCAGC[A/C]TGGGTGACAGGGTGA | 4666 |
rs540463828 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712175 | TAGCCAGGATGGTCT[C/T]AATCTCCTGACCTCG | 4666 |
rs540591460 | in-del | -/TA | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727827 | TTTAGGCAATTAACC[-/TA]TATATATATATTCAT | 4666 |
rs540846355 | snp | A/G | 1.96605e-05 | 0.00313526 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718066 | TTTGGGGAAGGAGGA[A/G]TTGCAGCTGGGGTTG | 4666 |
rs541003438 | snp | C/T | 0.000362552 | 0.013459 | intron-variant | NACA | GRCh38.p7 | 12:56714566 | TGATCAACCCTGCTT[C/T]TTTGACCCAATACCA | 4666 |
rs541185757 | snp | C/G | 3.69351e-05 | 0.00429723 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721384 | TGTGGGGCAGGAGAG[C/G]AAGGAGGGGGGAGGG | 4666 |
rs541218558 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56715556 | GAGCAAATGAAAAGG[C/G/T]CTGGCAGGTCTTGGT | 4666 |
rs541250988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721926 | TCCACCCAAATATCA[C/T]GAACAGAAAAGATAC | 4666 |
rs541284931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716164 | GGTGCTGCAGAGACA[C/G]ATGCTGATTCAGGTT | 4666 |
rs541286217 | in-del | -/GAG | | | intron-variant | NACA | GRCh38.p7 | 12:56721726 | CAACTATTTTAGGGT[-/GAG]GAGAACAGTCTAAGA | 4666 |
rs541908815 | in-del | -/TT | 0.00478085 | 0.0486577 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727837 | TAACCTATATATATA[-/TT]TTCATGTCAGTTTCC | 4666 |
rs541975611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716703 | AGGTGCCTCTTTGGG[C/G]GAAGGAGAAGTCACA | 4666 |
rs542012661 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726534 | CGCCTGCCTCGGCCT[C/T]CCAAACTACTGGGAT | 4666 |
rs542051135 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724633 | CTGTTAGAAAAAAAT[C/T]GTGAGGGTGTTTGGT | 4666 |
rs542178898 | snp | A/G | 1.70953e-05 | 0.00292359 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716050 | AGGGGTTTAGAGGGT[A/G]ATTCCAACACCAGCC | 4666 |
rs542371488 | snp | C/G | 1.75164e-05 | 0.00295937 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718780 | CGGGCCTTTTTGGGG[C/G]AGGAAGAAGTCATGG | 4666 |
rs542551399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722019 | AAAACACAGGCTTTT[A/T]TACTTTCAGGCTTCC | 4666 |
rs542829900 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | NACA | GRCh38.p7 | 12:56713071 | GTATACCTCTTCCTC[C/T]TCACTCTCCTCTTGT | 4666 |
rs542996726 | snp | C/T | 0.000799041 | 0.019972 | intron-variant | NACA | GRCh38.p7 | 12:56714730 | TTATAGTAGAAATTA[C/T]AAGAGAAGGTACTTC | 4666 |
rs543162537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713815 | CAAGAATAGAGAATG[C/G]GTTTTCTGCCGTAGT | 4666 |
rs543329259 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725384 | CGATTCCGGGTCAAG[A/G]GCTGCCGGCAGCCAC | 4666 |
rs543390709 | snp | C/T | 0.000466736 | 0.0152693 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719402 | GGGGGGATGGAGCCA[C/T]AGGGCAATTTTCTGA | 4666 |
rs543527270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720700 | GACTGAGTTGAAAGA[C/G]ATAAGGCAGCAGGTG | 4666 |
rs543739737 | snp | C/T | 0.000115042 | 0.00758338 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717162 | GGAGGATGGGGTAGC[C/T]GGGCCTCCTTTGGGG | 4666 |
rs543812736 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726364 | GCTCACTGCAATCTC[C/T]GCCTCCAGGGCTCAA | 4666 |
rs543828414 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722096 | AGGTGCACAGCACAA[C/T]TCAGTTCTTCCTAAA | 4666 |
rs544182420 | snp | A/G/T | 6.0242e-05 | 0.00548798 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718169 | GTGCCCCTTTGTGGG[A/G/T]TGGGGTAGCTAGACC | 4666 |
rs544365247 | snp | C/G | 0.000215998 | 0.01039 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717863 | GGGAGGGAGGAGTTG[C/G]AGCTGGGGTTGTGGG | 4666 |
rs544766829 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56724243 | AGAAAGCAAGCTAGG[G/T]TACTTTTAACGTCCA | 4666 |
rs544854374 | snp | G/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727483 | CACCGTGTTGCCCAG[G/T]CTGGTCTCGAACTCC | 4666 |
rs544936042 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715415 | TTTATGAAAAGGGAG[A/T]CCCTGGGCAACTGGT | 4666 |
rs544951704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56712967 | AATTTCAGCAGTTCT[C/T]TGGAGTCTCCTGAAT | 4666 |
rs545123765 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712394 | TTTTTTTTTTGGTGT[C/G]GGGGGGTGGCGGGGA | 4666 |
rs545209614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718219 | GTTGCAGCTGGGGGC[A/G]TGGGGGCCCCTTTGG | 4666 |
rs545380715 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726347 | GCAGTGGCACGATCT[A/C]GGCTCACTGCAATCT | 4666 |
rs545854602 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724136 | ATCTAGTTCCAATAG[A/G]TAAGAATCACTGAGC | 4666 |
rs546033694 | snp | A/G | 4.17388e-05 | 0.00456812 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717786 | TCCTTTTGGGGAGGG[A/G]GGAGTTGCAGCTGGG | 4666 |
rs546360887 | snp | A/G | 6.65447e-05 | 0.00576783 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716317 | TTCTGAACAGGGAGT[A/G]GAGGGGCTGGAGCCA | 4666 |
rs546693613 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714527 | CTTTATGAAGGTTCA[C/T]AGTTCCAAATACAAA | 4666 |
rs546695013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56723042 | AAGTCTAACGATTAC[A/G]GGAAAACGCTACCAA | 4666 |
rs546721072 | snp | C/T | 0.000252783 | 0.0112396 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716937 | TTTAGAGAGAAGAGT[C/T]GCTGTTGGGGCAATG | 4666 |
rs546787005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56721557 | TGCCTCCTAGGAAAC[A/G]CTGGAGTTTAAAATC | 4666 |
rs547750565 | snp | A/C/T | 0.000681493 | 0.018447 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720806 | TGACTTGAGGGGAAG[A/C/T]GATGGCTAGGGTAGT | 4666 |
rs547820885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56715159 | TAAACTGGGTTGGAG[A/G]AAGTCAAAAGCAGAC | 4666 |
rs547843864 | snp | G/T | 1.8337e-05 | 0.0030279 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715937 | TTCCAGCAGATTTAG[G/T]GGTGGGCATGTTGAC | 4666 |
rs547984143 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728022 | TAAAACTTAAAAAGT[C/T]TGTTACTATTAAATT | 4666 |
rs548442092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722549 | AAAAATTAGCTGGGC[A/G]TGGTGGTGTACACCT | 4666 |
rs548453622 | snp | A/G | 0.000146172 | 0.00854779 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715972 | ACCGACTGGAAAGGC[A/G]CTCCCCCAGAGATTG | 4666 |
rs548942275 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718960 | TTGGGGGATGGAGGA[A/G]TGGGAGAATGCGTCG | 4666 |
rs549300781 | snp | A/C | 0.00438332 | 0.0466095 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56711928 | TTAAGAAGGTCCTAA[A/C]AGCCTAGTATAGTAA | 4666 |
rs549414991 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725106 | TGCCAGGACACCAAC[C/G]GCAGACCCCATTTTG | 4666 |
rs549476423 | snp | C/G | 1.66488e-05 | 0.00288515 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719614 | GTTGGGGTAATGAGA[C/G]AACTTTTGAGAAGCG | 4666 |
rs549541384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56713971 | CTCAGCCACCTTAGT[A/G]GCTGGGATTACAGGA | 4666 |
rs549577760 | snp | C/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719033 | CTGGAAGAAATGAAG[C/T]TTCAACTGGAGAAAC | 4666 |
rs549642565 | snp | G/T | 0.00118992 | 0.0243628 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712584 | ATAATTAGCGGTTCT[G/T]ATAGGCAAATCAGGA | 4666 |
rs549702269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713309 | GTACAGCTTTAAACT[A/G]CTTGCCCTCACAGTA | 4666 |
rs550194044 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725844 | CGATTTTTCTTGTTC[C/T]GTTCAATGACTAGAG | 4666 |
rs550255490 | snp | C/T | 1.66424e-05 | 0.0028846 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719692 | GCCGAGGAGTTAACA[C/T]CCAGAGGGGAGGTCA | 4666 |
rs550275636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714969 | CTTTCTTTCCCTCAA[A/G]GTCTTTGTTTCTTGG | 4666 |
rs550397762 | in-del | -/ATTAA | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727904 | AGGATTGTTTGGAAG[-/ATTAA]ATTAGTCTGTGTGTA | 4666 |
rs550451456 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726575 | AGCCACCATGCCCAG[C/T]CTGTTTGTTTTGTTT | 4666 |
rs550467533 | snp | A/G | 0 | 0 | intron-variant | NACA | GRCh38.p7 | 12:56722760 | CCACTCCTTAACTTG[A/G]AATTTAAGTGTTTCA | 4666 |
rs550665974 | snp | A/G | 1.95437e-05 | 0.00312593 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718375 | GGGGCCCCTTTGGGG[A/G]GTGGGGTAGCTGCTG | 4666 |
rs550672821 | snp | C/T | 0.00327286 | 0.0403202 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717536 | CTGGGGGAGTGGGGG[C/T]CCCTTTGGGGGGTGG | 4666 |
rs550993630 | in-del | -/ACTC | | | intron-variant | NACA | GRCh38.p7 | 12:56724820 | CCCTCCACTCCTAAT[-/ACTC]ACACTGGCTGGGCTG | 4666 |
rs551054876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718041 | TGGGGGTGGGGTAGC[C/T]AGACCTCCTTTTGGG | 4666 |
rs551249413 | snp | C/G/T | 5.89134e-05 | 0.00542714 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717941 | GAGTTGCAGCTGGGG[C/G/T]TGTGGGGGCCCCTTT | 4666 |
rs551443589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713345 | AGTAGTTGTTTAGGT[A/T]TAGAGCAGTGGTTCT | 4666 |
rs551627714 | snp | A/T | 3.58301e-05 | 0.00423247 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718914 | TCCTTTGGGAGACAG[A/T]GGAGTCACAGCTGAG | 4666 |
rs551776881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713928 | CTCAATGTAATGTCC[A/G]TCTCCCAGGTTCAAG | 4666 |
rs551888616 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725079 | CGCCCCGCAGCCCTT[C/G]TACCCTGCTTTTGCC | 4666 |
rs551974642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724609 | TATTCTTAAAAACTC[C/T]GAGGAGGGCTGTTAG | 4666 |
rs552236333 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727747 | TCAAATAGGAGAGGC[A/G]ATATTGTGGAGTCAT | 4666 |
rs552274711 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724950 | ACAGGTTCTAAGGCT[A/G]TGACCCCTTACCCTT | 4666 |
rs552343056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56721592 | AGTCTAAGTCACCAC[A/G]CAGGATTAGATAAAG | 4666 |
rs552351428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722328 | AGAGCTTACTCACAA[C/G]GGTAGGGACTGTATT | 4666 |
rs552914942 | snp | C/T | 1.95662e-05 | 0.00312773 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717667 | GTTACAACTGCGGGA[C/T]TGGGGGCCCCTTTGT | 4666 |
rs552920572 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56722523 | TGAAACCCCGTCTCT[A/C]CTAAAAATACAAAAA | 4666 |
rs552996972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715568 | AGGTCTGGCAGGTCT[G/T]GGTTTTCAATGTCAG | 4666 |
rs553031065 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725997 | TATGTTCCAACCTTG[C/T]ATGGATAACGTAATC | 4666 |
rs553055862 | snp | A/C/G | 0.000133804 | 0.00817844 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717178 | GGGCCTCCTTTGGGG[A/C/G]CTGAAGTTGCTGGGG | 4666 |
rs553180254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721967 | AACAAAGAAGTTAGT[A/G]AGCAGTGACGATGAT | 4666 |
rs553297899 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728160 | GACAAAAGTACATAT[A/T]CACAATTTTTCTTTC | 4666 |
rs553446059 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725277 | CTGTGCAGGGAACGC[C/G]GAACCAAGATGGCGG | 4666 |
rs553458607 | snp | A/G | 1.74187e-05 | 0.00295111 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719167 | GAATCAGCTAGGTAA[A/G]TCAGAGTTCCTTTGG | 4666 |
rs554245378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714290 | CCTGTTCCCCAAAAA[C/T]CTATGGAAATAAACA | 4666 |
rs554845654 | in-del | -/G | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725214 | CGGCTTAGCCCGAAA[-/G]AAAGGCGGATGGCTG | 4666 |
rs554882653 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723368 | AATTTCAAATCTTCG[C/T]ATTTGTAAAATTAAG | 4666 |
rs554973931 | snp | A/G | 1.67262e-05 | 0.00289185 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721123 | GCAACCAGAGCTAAG[A/G]GAGCTGAAGAGGAAG | 4666 |
rs555128855 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722002 | AATCTGAACTGAATA[A/G]GAAAACACAGGCTTT | 4666 |
rs555857821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718653 | TGTGGGGGCCCATTT[C/T]GGGGATGGGGTAGCT | 4666 |
rs555996764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724800 | TTCAGACGCTACTGT[A/G]AACCCCCTCCACTCC | 4666 |
rs556017550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724682 | ACCTGGGAATAAGAG[A/G]TAAATATGATGTGAC | 4666 |
rs556100472 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718542 | AGCTGGACCTCCTTT[G/T]GGGGAGGGAGGAGTT | 4666 |
rs556220513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56724090 | TGCTGGCTGGAGTTT[C/T]ACAAATGCTCCGGGC | 4666 |
rs556433678 | in-del | -/T | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712375 | TAGAACCTTTTTAAG[-/T]TTTTTTTTTTTTTGG | 4666 |
rs556518624 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56712961 | AAGAACAATTTCAGC[A/C]GTTCTTTGGAGTCTC | 4666 |
rs556881553 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | NACA | GRCh38.p7 | 12:56713020 | AACACGAACACAATG[C/T]TATACGGCGAGAGTT | 4666 |
rs556902858 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712111 | AGGTGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 4666 |
rs556943166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713470 | AGAACTATCTGACGC[A/G]AAATGTCAGCAGTGC | 4666 |
rs557025513 | snp | C/G | 1.98022e-05 | 0.00314654 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717711 | TAGACCTCCTTTTAG[C/G]GAGGGAGGAGTTGCA | 4666 |
rs557107249 | snp | C/T | 1.9265e-05 | 0.00310357 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717257 | TGGATGGGGTGGCTG[C/T]GCCTTCTCTGGTGAC | 4666 |
rs557295893 | snp | C/G | 1.66313e-05 | 0.00288364 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716429 | TCTGTGGACCTTTCC[C/G]AGTGGGAGCTGTGAT | 4666 |
rs557754386 | snp | A/G | 1.92922e-05 | 0.00310575 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717076 | GGAGAGGAAGAAGTG[A/G]CAACTTGTTTGGGGG | 4666 |
rs557953707 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712156 | AGACGGGGTTTCAAC[A/G]TGTTAGCCAGGATGG | 4666 |
rs558038375 | snp | G/T | 0.110519 | 0.207473 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718148 | GAGTTGCAGCTGGGG[G/T]TGTGGGTGCCCCTTT | 4666 |
rs558038898 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725508 | CAGGAGCTCTCTGCG[C/T]GGACCCACGCAGTCC | 4666 |
rs558164717 | snp | G/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727602 | GGAAGCAGTGAAAAT[G/T]TAAAATGCTTTGAAA | 4666 |
rs558275964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712662 | CCACTAAAACCTATA[C/T]GGCAACTCAGAAGAG | 4666 |
rs558484170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723388 | GTAAAATTAAGTTGT[C/T]CAATGACACAATCTC | 4666 |
rs558496964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723864 | ACGCTGAGGATAAAA[A/G]GATTTATTTCAATCC | 4666 |
rs558606733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715438 | CAACTGGTCATTACT[A/G]AGTCTAATAATGGAA | 4666 |
rs558882061 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716469 | GCTTTCTGGAGCTGG[A/G]GCAACAAGTACTTCT | 4666 |
rs558889674 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726225 | AGATTCTCCTTCCCA[C/G]AAAAAAAGAACATAG | 4666 |
rs558900230 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727124 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTTACT | 4666 |
rs559018586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721819 | ATCCTTTCCCAGTTG[C/T]GCCCTCCCCTTACTT | 4666 |
rs559098569 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715265 | TCAATGATGATGACC[C/T]ATATCTCTAGTTTTT | 4666 |
rs559439219 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724241 | ATAGAAAGCAAGCTA[A/C/G]GGTACTTTTAACGTC | 4666 |
rs559475975 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722345 | GTAGGGACTGTATTA[C/T]GAAACTGTAACCTAA | 4666 |
rs559590703 | snp | C/G | 1.64866e-05 | 0.00287106 | splice-acceptor-variant | NACA | GRCh38.p7 | 12:56714688 | ATTCTGTTCCAGACC[C/G]TAAGATGAGAAACAA | 4666 |
rs559972022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723731 | CCTTCATTTAACGCT[A/G]CACAACTGACTCAGA | 4666 |
rs559982408 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712396 | TTTTTTTTGGTGTGG[A/G]GGGGTGGCGGGGAAG | 4666 |
rs560034080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724253 | CTAGGGTACTTTTAA[A/C]GTCCACGAATCTTAA | 4666 |
rs560117011 | snp | A/G | 7.88441e-05 | 0.0062782 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718238 | GGGCCCCTTTGGGGG[A/G]TGGGGTAGCTGGGCC | 4666 |
rs560184409 | snp | C/G/T | 7.03982e-05 | 0.00593252 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718765 | GGGGCTGGAGTTGCT[C/G/T]GGGCCTTTTTGGGGG | 4666 |
rs560315478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713947 | CCCAGGTTCAAGCAA[C/T]TGCCGTGCCTCAGCC | 4666 |
rs560586465 | snp | C/T | 0.000466332 | 0.0152627 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719576 | CGGCAGGGTCAGCAC[C/T]TTCCAAAGGAAATGC | 4666 |
rs560638525 | snp | C/T | 0.000399281 | 0.0141238 | missense | NACA | GRCh38.p7 | 12:56713649 | GTGACTCTAGTAACT[C/T]CTGTAACCTGCCGAA | 4666 |
rs560863822 | snp | C/T | 1.75745e-05 | 0.00296428 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718826 | GTTTGGGTGCTGGAG[C/T]AGCTGGACCCTCTTT | 4666 |
rs561183003 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56721904 | AAGAACAGCTGTGCT[-/A]ACTCTGTCCACCCAA | 4666 |
rs561240723 | snp | A/G | 1.66726e-05 | 0.00288722 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720691 | ACAGGAAGAGACTGA[A/G]TTGAAAGAGATAAGG | 4666 |
rs561366479 | snp | G/T | 1.66294e-05 | 0.00288347 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720272 | AATGATAAGTGGCAT[G/T]AGGAGAGCTTTTGAG | 4666 |
rs561719305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722686 | GACAGGGTGAGACTC[C/T]GTCTCAAAACAAAAC | 4666 |
rs561780372 | snp | G/T | 2.02932e-05 | 0.00318531 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717443 | CCTCTTTGGAGGATG[G/T]AGTAGTTGGGCCTCC | 4666 |
rs561780660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723478 | CCTTCCTTAAGCCCC[C/T]TGTACTTCAAGAATT | 4666 |
rs562232817 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56724634 | TGTTAGAAAAAAATC[C/G]TGAGGGTGTTTGGTG | 4666 |
rs562260931 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727132 | CAGTGGCGCGATCTC[A/G]GCTTACTGCAACCTC | 4666 |
rs562442625 | snp | A/G | 0.000215553 | 0.0103793 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717895 | GCCCCTTTGGGGGAT[A/G]GGGTAGCTAGACCTC | 4666 |
rs562614564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718198 | CCTCCTTTTGGGGAG[A/G]GAGGAGTTGCAGCTG | 4666 |
rs562822014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722817 | CATGACAGTAAGACA[A/G]TATCTCTGGCATTCA | 4666 |
rs562934435 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725441 | GTTCCCACGGCGGGG[G/T]TGGTGACAAGGACTA | 4666 |
rs563600871 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727502 | GTCTCGAACTCCTGA[A/G]CTCAGGCAATCCACC | 4666 |
rs564103011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722640 | TTGCAGTGAGCCAAG[A/G]TCGCGCTACTGCATG | 4666 |
rs564142402 | snp | G/T | 3.94984e-05 | 0.00444383 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716830 | GCTGGGGCTTCTTTG[G/T]GGGTTGGAATTGCTG | 4666 |
rs564621032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717351 | GGGAGATGGGATAGC[G/T]GGTCCTCTTTTGGGG | 4666 |
rs564713071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714494 | GATCTGGATAGCACA[A/G]TCTCCTTGTGGGTTT | 4666 |
rs564833693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56713311 | ACAGCTTTAAACTGC[C/T]TGCCCTCACAGTAGA | 4666 |
rs564841699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56713816 | AAGAATAGAGAATGG[C/G]TTTTCTGCCGTAGTA | 4666 |
rs565179983 | snp | C/G | 6.80585e-05 | 0.00583306 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719430 | TGAAGCTGTAGGAAC[C/G]AAGGGTAAAGTAGTA | 4666 |
rs565196909 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726591 | CTGTTTGTTTTGTTT[C/T]TGGGACAGTCTCACT | 4666 |
rs565315014 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726785 | TCCATGTTGGCCAGG[A/C]TGGTCTCCTCCTGAC | 4666 |
rs565506631 | snp | A/G | 1.66665e-05 | 0.00288669 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720701 | ACTGAGTTGAAAGAG[A/G]TAAGGCAGCAGGTGG | 4666 |
rs565771139 | snp | A/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727780 | AAGACAGACTCTGAA[A/T]TAAGACTCCTTTGTC | 4666 |
rs565807775 | snp | A/G | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725001 | TTCCCAAAACAAGAC[A/G]CACTCCTCTTCCGCC | 4666 |
rs566115246 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728161 | ACAAAAGTACATATT[A/C]ACAATTTTTCTTTCT | 4666 |
rs566257074 | snp | A/G | 1.84749e-05 | 0.00303926 | intron-variant | NACA | GRCh38.p7 | 12:56715850 | AGACACACCATGCAC[A/G]CGGCAAACCAAGGCA | 4666 |
rs566775915 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717942 | AGTTGCAGCTGGGGT[C/T]GTGGGGGCCCCTTTG | 4666 |
rs566973533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56713348 | AGTTGTTTAGGTTTA[A/G]AGCAGTGGTTCTCAA | 4666 |
rs567048385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724616 | AAAAACTCCGAGGAG[A/G]GCTGTTAGAAAAAAA | 4666 |
rs567109246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718483 | CCTTTGGGGGAGGGA[G/T]GAGTCACAGCTGGGG | 4666 |
rs567238579 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712476 | ATGATAGAAACAGTA[A/C]AAATTTCAAACCAAG | 4666 |
rs567786563 | snp | A/G | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712449 | ATCCAACAAGAAGCC[A/G]TAACTTTATTTATGA | 4666 |
rs568115356 | snp | C/T | 0.000272072 | 0.0116603 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716940 | AGAGAGAAGAGTCGC[C/T]GTTGGGGCAATGGGG | 4666 |
rs568150891 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718010 | GAGTTGCAGCTGGGG[G/T]TGTGGGGGCCCCTTT | 4666 |
rs568263055 | snp | A/G | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725253 | CAGTAGCGGCACAGA[A/G]AGTACTTACTGTGCA | 4666 |
rs568300214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722314 | AGACCTCCAGGCAGA[C/G]AGCTTACTCACAAGG | 4666 |
rs568438540 | snp | G/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722809 | ATGTTTGGCATGACA[G/T]TAAGACAGTATCTCT | 4666 |
rs568707823 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726015 | GGATAACGTAATCCA[C/G]CTAAAAACTCCTCTG | 4666 |
rs569066313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717573 | TGGGCTTCCTTTTGG[A/G]GAGGGAGGAGTTGCA | 4666 |
rs569213943 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718059 | ACCTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs569290479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724589 | TTGCCCAACCCGGAG[A/G]TAAGTATTCTTAAAA | 4666 |
rs569347472 | snp | C/T | 0.00010898 | 0.00738093 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715985 | GCACTCCCCCAGAGA[C/T]TGGTTCCGGGGGAAT | 4666 |
rs569353044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718376 | GGGCCCCTTTGGGGA[A/G]TGGGGTAGCTGCTGG | 4666 |
rs569436510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715408 | CTACATTTTTATGAA[A/G]AGGGAGTCCCTGGGC | 4666 |
rs569609748 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727950 | ACACACTCACACTCT[A/T]ATTGGAAGGAAAAAG | 4666 |
rs569694435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720376 | CTAGAGATGGTAGAG[A/G]GACCTTTGTCAACAG | 4666 |
rs569879952 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726996 | ATGAAAAGCCTCCCA[C/T]ATCTTCCCACAGCCC | 4666 |
rs570078813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56721762 | GCCTATCTCTAAATG[C/G]GGAGCACAGACTCTT | 4666 |
rs570349482 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712434 | TCACCGACTGAATTC[A/C]TCCAACAAGAAGCCA | 4666 |
rs570406970 | snp | A/G | 7.98037e-05 | 0.00631629 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721450 | AAGGCTGAAGACATA[A/G]GTAGCACAGCTGGAG | 4666 |
rs570469875 | snp | C/G | 0.000333595 | 0.0129107 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716253 | AGGAGCCAAGGGGCC[C/G]TTTGGGGAATGAGAA | 4666 |
rs570492489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722438 | CTCATGCCTGTAATC[C/T]CAGCACTTCGGGATG | 4666 |
rs570553287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACA | GRCh38.p7 | 12:56722994 | AAAAGACAAGGTGGC[C/T]CAACTAGTTTTTCCT | 4666 |
rs570669427 | snp | A/G | 1.66338e-05 | 0.00288386 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720927 | TGGAGGGCTGGGGGT[A/G]CCTTTTGGATTAGGG | 4666 |
rs570724842 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727331 | TAAGACGACTGTGGC[C/T]ACCTTTTTTTTTTTT | 4666 |
rs570866733 | snp | A/G/T | 0.000134938 | 0.00821305 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717116 | CCTTGGGGGAAGGAG[A/G/T]AGTCACTGCTGGGAG | 4666 |
rs570890246 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725263 | ACAGAAAGTACTTAC[C/T]GTGCAGGGAACGCGG | 4666 |
rs570955364 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725853 | TTGTTCTGTTCAATG[A/G]CTAGAGAGACTCAAA | 4666 |
rs571505600 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712354 | TAGGAGTAATTAATA[A/C]ATTACTAGAACCTTT | 4666 |
rs571781234 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACA | GRCh38.p7 | 12:56714987 | CTTTGTTTCTTGGCA[A/C]AGGCAAATAATGACC | 4666 |
rs571854188 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720233 | TTCCAACAGAAGAAA[C/T]GGGCATTTGGGCCAC | 4666 |
rs571898362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56724838 | CACACTGGCTGGGCT[A/G]GGGCCTCCTGGACTA | 4666 |
rs571910780 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725291 | CGGAACCAAGATGGC[A/G]GCAGAAAGACCGAGC | 4666 |
rs571910842 | snp | A/C/G/T | 0.000105241 | 0.00725341 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718776 | TGCTCGGGCCTTTTT[A/C/G/T]GGGGAGGAAGAAGTC | 4666 |
rs571929667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714096 | AAGTGATCCATCTGC[C/T]TTGGCCTTCCAGTGT | 4666 |
rs571953339 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723418 | CTAAAATCTCGTTTT[A/G]TACTGAAATTACAGA | 4666 |
rs571985471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714199 | AATTGGGTTCAGTGT[A/G]TACTGCTTGGGTGAC | 4666 |
rs572194163 | snp | C/T | 0.000188817 | 0.00971457 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716033 | CCTCATCAGCAGGGG[C/T]AAGGGGTTTAGAGGG | 4666 |
rs572272326 | snp | C/G | | | intron-variant | NACA | GRCh38.p7 | 12:56721593 | GTCTAAGTCACCACG[C/G]AGGATTAGATAAAGG | 4666 |
rs572335720 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727466 | CAAAACTTCTCCTGT[G/T]TCACCGTGTTGCCCA | 4666 |
rs572547208 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726386 | AGGGCTCAAGCAGTT[G/T]TCCCGCCTCAGCCTC | 4666 |
rs572864607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56722644 | AGTGAGCCAAGATCG[C/T]GCTACTGCATGCACT | 4666 |
rs572879021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723410 | CACAATCTCTAAAAT[A/C]TCGTTTTGTACTGAA | 4666 |
rs573039769 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726317 | TTTGAGTCGCTCTGT[C/T]GGCCAGGCTAGAGTG | 4666 |
rs573361026 | snp | A/C/T | 0.110519 | 0.207473 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718149 | AGTTGCAGCTGGGGT[A/C/T]GTGGGTGCCCCTTTG | 4666 |
rs573422314 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712168 | AACGTGTTAGCCAGG[A/G]TGGTCTCAATCTCCT | 4666 |
rs573542498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723878 | AGGATTTATTTCAAT[C/T]CTGGGTTTCACACAA | 4666 |
rs573566534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACA | GRCh38.p7 | 12:56724024 | CATCTCATCCAGACA[C/T]GTGATAAAGGCACAA | 4666 |
rs573624682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56723669 | ATAACAAATGAAATT[A/T]AAAAAAAACCAAAAA | 4666 |
rs574346227 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712247 | AGGCGTGAGCCACCA[C/T]GCCTGGCCAGTAACT | 4666 |
rs574552110 | snp | A/G | 1.90503e-05 | 0.00308623 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717205 | GGGGCCTTTTTGAGG[A/G]AGACAGGAGTCACTG | 4666 |
rs574662799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716047 | GCAAGGGGTTTAGAG[G/T]GTGATTCCAACACCA | 4666 |
rs574710963 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723583 | AAATCAAACAGGTGG[A/G]AAGAAACTTTATGCT | 4666 |
rs574713860 | in-del | -/A | | | intron-variant | NACA | GRCh38.p7 | 12:56722038 | TTTCAGGCTTCCACT[-/A]GGCTAGGAAACATCT | 4666 |
rs574744361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACA | GRCh38.p7 | 12:56715601 | CAATTAGGTAAAATA[A/G]ATGGCATGGCAGGCT | 4666 |
rs575166407 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | NACA | GRCh38.p7 | 12:56722454 | CAGCACTTCGGGATG[A/C/T]CTGGGAGGGCGGATC | 4666 |
rs575729172 | snp | C/G | 3.95163e-05 | 0.00444484 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717295 | GCTGGAGCCTTTTTG[C/G]GGGAGAGAGGAATCA | 4666 |
rs575816096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56722516 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 4666 |
rs575877258 | snp | C/T | 3.33195e-05 | 0.0040815 | intron-variant | NACA | GRCh38.p7 | 12:56713722 | GGTTTTCAACCTCTT[C/T]AGAAGCAGCCTAAAG | 4666 |
rs576140603 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56726176 | TTGTTTTAGGTTCAC[A/G]ACAATTTAGCCGATG | 4666 |
rs576191669 | in-del | -/GTCA | 0.00358779 | 0.0422022 | intron-variant | NACA | GRCh38.p7 | 12:56713475 | TATCTGACGCAAAAT[-/GTCA]GCAGTGCTGAGGTTG | 4666 |
rs576257407 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725329 | TGACCCACGCCTGTT[A/G]CAGAAGGAAGCCTGG | 4666 |
rs576429405 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728266 | TTTTTTTTTTTTGAG[A/G]CAGGGTCTGGCTCTG | 4666 |
rs576452596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720699 | AGACTGAGTTGAAAG[A/G]GATAAGGCAGCAGGT | 4666 |
rs576551678 | snp | C/G | 3.3724e-05 | 0.0041062 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716090 | ACGGCAGAAATTGCT[C/G]TTTAGGAGGCAGAGT | 4666 |
rs576585362 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727531 | CCCGCTTCGGCCTCC[C/T]ATAGTGCTAGGATTA | 4666 |
rs576890900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56721902 | GAGAAGAACAGCTGT[G/T]CTACTCTGTCCACCC | 4666 |
rs576949246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714530 | TATGAAGGTTCACAG[C/T]TCCAAATACAAAAGT | 4666 |
rs577007618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56715523 | GGACAAGGTTAGTTA[A/G]TGATGTGGTAGGGAT | 4666 |
rs577145616 | snp | C/T | 0.000100471 | 0.00708697 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716529 | AAGCCCTTTAGATGC[C/T]TGAGGAACAGTGGCC | 4666 |
rs577185452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACA | GRCh38.p7 | 12:56714007 | ACCACCATGCCCTGC[C/T]ATATATTTTTGGTAT | 4666 |
rs577634104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718218 | AGTTGCAGCTGGGGG[C/T]ATGGGGGCCCCTTTG | 4666 |
rs577915424 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726332 | CGGCCAGGCTAGAGT[A/G]CAGTGGCACGATCTC | 4666 |
rs578149591 | snp | C/T | 1.67052e-05 | 0.00289004 | intron-variant | NACA | GRCh38.p7 | 12:56713502 | GAGGTTGAGAAACCC[C/T]GGTCTGGAACAATGC | 4666 |
rs745329882 | in-del | -/TTGGGGAGGGAGGAGTTG | 1.98281e-05 | 0.0031486 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718121 | TAGCTAGACCTCCTT[-/TTGGGGAGGGAGGAGTTG]CAGCTGGGGTTGTGG | 4666 |
rs745368102 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720119 | CTATGTTACTTATGG[A/G]ACCTGATGACATTGG | 4666 |
rs745383357 | in-del | -/AA | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712468 | CTTTATTTATGATAG[-/AA]ACAGTACAAATTTCA | 4666 |
rs745387506 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56717682 | TTGGGGGCCCCTTTG[G/T]GGGGTGGGGTAGCTA | 4666 |
rs745434747 | snp | A/G | 1.96219e-05 | 0.00313218 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718006 | GGAGGAGTTGCAGCT[A/G]GGGTTGTGGGGGCCC | 4666 |
rs745582137 | in-del | -/TGGGGGCCCCTT | 5.9199e-05 | 0.00544022 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718220 | TTGCAGCTGGGGGCA[-/TGGGGGCCCCTT]TGGGGGATGGGGTAG | 4666 |
rs745624948 | snp | G/T | 1.92184e-05 | 0.00309981 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717253 | CCTTTGGATGGGGTG[G/T]CTGCGCCTTCTCTGG | 4666 |
rs745641051 | snp | C/G | 0.000166861 | 0.00913251 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719487 | TTTAGGAGCTAAAGA[C/G]ACAGTTCCTTCTAGA | 4666 |
rs745686231 | snp | A/G | 6.14043e-05 | 0.00554061 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717338 | TGGGGTCCCCTTTGG[A/G]AGATGGGATAGCTGG | 4666 |
rs745713255 | snp | C/T | 3.35469e-05 | 0.0040954 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716172 | AGAGACAGATGCTGA[C/T]TCAGGTTTAGGAAGG | 4666 |
rs745758153 | snp | C/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720858 | GGAGGCCACTCCAGA[C/T]TGAATAGAGGCCATG | 4666 |
rs745779934 | snp | A/G | 1.66888e-05 | 0.00288862 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716247 | CTCAGGAGGAGCCAA[A/G]GGGCCCTTTGGGGAA | 4666 |
rs745786935 | snp | C/T | 1.83474e-05 | 0.00302876 | intron-variant | NACA | GRCh38.p7 | 12:56713208 | ACAGGGTAGAAAATA[C/T]AGATCCATGTGAGTA | 4666 |
rs745861655 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56722197 | TACTCACAAAACCCA[A/C]ACAAGAAAACCAACC | 4666 |
rs745914224 | in-del | -/AG | 1.72234e-05 | 0.00293452 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719049 | TTCAACTGGAGAAAC[-/AG]GGGATGAGAGATTTC | 4666 |
rs745924545 | snp | C/T | 2.78447e-05 | 0.00373116 | intron-variant | NACA | GRCh38.p7 | 12:56724449 | GAGGGTAGGGAAACC[C/T]ACCTGTCTCAGCCTG | 4666 |
rs745940530 | snp | A/T | 1.78417e-05 | 0.00298673 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718855 | TTGGGGAAGGGCAGA[A/T]TCACCACTGAAGGAG | 4666 |
rs745989049 | snp | C/T | 1.97346e-05 | 0.00314116 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716843 | TGGGGGTTGGAATTG[C/T]TGGGGTCTTTTTAGG | 4666 |
rs746002980 | snp | A/G | 2.08166e-05 | 0.00322613 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717799 | GGAGGAGTTGCAGCT[A/G]GGGTTGTGGGGGCCC | 4666 |
rs746013373 | snp | G/T | 2.069e-05 | 0.0032163 | intron-variant | NACA | GRCh38.p7 | 12:56721462 | ATAGGTAGCACAGCT[G/T]GAGAAAGGCAAAAGG | 4666 |
rs746083220 | snp | A/G | 0.000117158 | 0.00765279 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716901 | GAGGGCCTCTTTGGG[A/G]GCTAGAGTTGCTGGG | 4666 |
rs746128868 | snp | A/G | 1.66374e-05 | 0.00288417 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719901 | TTGGGCTGGAGAGAA[A/G]GGGGCTCCTTCAAGA | 4666 |
rs746261226 | snp | G/T | 1.81737e-05 | 0.00301439 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715983 | AGGCACTCCCCCAGA[G/T]ATTGGTTCCGGGGGA | 4666 |
rs746275223 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723839 | TTAGCCTTCACAGTC[A/G]TTAATTTCGACGCTG | 4666 |
rs746310279 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56715745 | TTATCATTCTATGTT[A/C]TACATCCAAACCCAA | 4666 |
rs746373754 | in-del | -/CCT | 3.92261e-05 | 0.00442849 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717631 | GGTGAGGTAGCTGGG[-/CCT]CCTTTTGGAGAGGGA | 4666 |
rs746376721 | snp | A/G | 1.94445e-05 | 0.00311799 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718411 | CCTTTGGGGGAGGGA[A/G]GAGTTGCAGCTGGGG | 4666 |
rs746403095 | snp | A/G | 5.22407e-05 | 0.00511054 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719163 | TGGGGAATCAGCTAG[A/G]TAAGTCAGAGTTCCT | 4666 |
rs746426761 | in-del | -/G | 1.96678e-05 | 0.00313584 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716782 | GAAGGAGTCACTGCT[-/G]GGGGACTGGAGGCCT | 4666 |
rs746461737 | in-del | -/GGAGCACAGGTATTCTGGGGGGAT | 8.77678e-05 | 0.00662391 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56719371 | ACTAAGGTAGCCAGA[-/GGAGCACAGGTATTCTGGGGGGAT]GGAGCCACAGGGCAA | 4666 |
rs746462700 | snp | C/T | 5.93948e-05 | 0.00544921 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717565 | GGGGTACCTGGGCTT[C/T]CTTTTGGGGAGGGAG | 4666 |
rs746471255 | snp | C/T | 4.98931e-05 | 0.00499441 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716428 | GTCTGTGGACCTTTC[C/T]GAGTGGGAGCTGTGA | 4666 |
rs746518354 | snp | A/G | 1.7265e-05 | 0.00293806 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719071 | GAGAGATTTCCAATA[A/G]GAGTATCAGGGCCAG | 4666 |
rs746533878 | snp | G/T | 1.67621e-05 | 0.00289495 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716533 | CCTTTAGATGCTTGA[G/T]GAACAGTGGCCCCCA | 4666 |
rs746584701 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724695 | AGGTAAATATGATGT[A/G]ACCCTCACGCCTCTA | 4666 |
rs746597467 | snp | C/T | 1.66291e-05 | 0.00288345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720248 | CGGGCATTTGGGCCA[C/T]TAAAGGATAATGATA | 4666 |
rs746621448 | snp | A/G | 1.65318e-05 | 0.002875 | intron-variant | NACA | GRCh38.p7 | 12:56714477 | AGTTAACCAGAATCT[A/G]AGATCTGGATAGCAC | 4666 |
rs746653744 | in-del | -/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722365 | CTGTAACCTAACTTG[-/T]TAAACCAGATTGTGG | 4666 |
rs746681617 | snp | A/G | 1.74561e-05 | 0.00295428 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721344 | GAATGGGGAAGCCTG[A/G]TTAGCAGCTGAGAGA | 4666 |
rs746709271 | in-del | -/TTTATTT | | | intron-variant | NACA | GRCh38.p7 | 12:56713843 | AGTAACTTCTGTTAC[-/TTTATTT]TTTATTTTTTGGAGG | 4666 |
rs746751293 | snp | G/T | 4.94376e-05 | 0.00497156 | missense | NACA | GRCh38.p7 | 12:56714674 | TTCATCACTGTCAGA[G/T]TCTGTTCCAGACCCT | 4666 |
rs746760859 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718427 | GAGTTGCAGCTGGGG[G/T]TGTGGATGCCCCTTT | 4666 |
rs746771277 | snp | G/T | 5.02105e-05 | 0.00501026 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721261 | GTTCCCAAAGGTAGG[G/T]CTGTTCCAGAGGATG | 4666 |
rs746773697 | snp | A/G | 1.95766e-05 | 0.00312856 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717987 | TAGACCTCCTTTTGG[A/G]GAAGGAGGAGTTGCA | 4666 |
rs746818458 | snp | C/G | 1.66643e-05 | 0.0028865 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720574 | CCTAAAAGTTGGACA[C/G]AACCAAAAGAACTCT | 4666 |
rs746845014 | snp | C/G | 1.9214e-05 | 0.00309945 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717148 | GTGGGATCCCCTTTG[C/G]AGGATGGGGTAGCTG | 4666 |
rs746891002 | snp | C/T | 1.66493e-05 | 0.0028852 | intron-variant, splice-acceptor-variant, missense | NACA | GRCh38.p7 | 12:56719597 | AAGGAAATGCAGCCA[C/T]TGTTGGGGTAATGAG | 4666 |
rs746908006 | in-del | -/CA | 7.77197e-05 | 0.00623328 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718427 | AGTTGCAGCTGGGGG[-/CA]TGTGGATGCCCCTTT | 4666 |
rs746911757 | snp | A/G | 1.91514e-05 | 0.0030944 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717243 | AGTGAGATCTCCTTT[A/G]GATGGGGTGGCTGCG | 4666 |
rs746930752 | snp | A/C | 0.000135051 | 0.00821627 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716082 | AGGAGAGGACGGCAG[A/C]AATTGCTGTTTAGGA | 4666 |
rs746982131 | snp | C/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719540 | AAGTTGAGGTACCTT[C/T]GGCAGTTGTGGGAGC | 4666 |
rs746982163 | snp | A/T | 3.33622e-05 | 0.00408412 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719493 | AGCTAAAGAGACAGT[A/T]CCTTCTAGAAAAGGG | 4666 |
rs747020698 | snp | A/G | 1.6793e-05 | 0.00289763 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716148 | AGAGACTGGTGGGGA[A/G]GGTGCTGCAGAGACA | 4666 |
rs747052068 | snp | A/G | 1.96027e-05 | 0.00313065 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718528 | TTGGGGGATGGAGTA[A/G]CTGGACCTCCTTTGG | 4666 |
rs747142033 | snp | A/G | 0.000118168 | 0.00768572 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718622 | CTTTTGGGGAGGGAG[A/G]AGTTGCAGCTGGGGG | 4666 |
rs747143650 | snp | G/T | 1.95685e-05 | 0.00312792 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717660 | GGGAGGAGTTACAAC[G/T]GCGGGATTGGGGGCC | 4666 |
rs747185124 | snp | A/G | 8.32494e-05 | 0.00645118 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720558 | ACTAGGACCTGTTTG[A/G]CCTAAAAGTTGGACA | 4666 |
rs747227914 | snp | A/T | 1.98257e-05 | 0.00314841 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717723 | TAGGGAGGGAGGAGT[A/T]GCAGCTGGGGGAGTG | 4666 |
rs747271646 | in-del | -/G | 2.11463e-05 | 0.00325157 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717737 | TGCAGCTGGGGGAGT[-/G]GGGGGCCCCTTTGGG | 4666 |
rs747367803 | snp | C/G/T | 3.68917e-05 | 0.00429473 | intron-variant | NACA | GRCh38.p7 | 12:56715845 | ACGACAGACACACCA[C/G/T]GCACACGGCAAACCA | 4666 |
rs747387694 | snp | A/G | 1.66291e-05 | 0.00288345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720002 | GGTCTTCAGGGTCTG[A/G]CAGAGGAGGAGAGAC | 4666 |
rs747432522 | snp | A/G | 5.86573e-05 | 0.00541528 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716890 | GCTGGGGGAATGAGG[A/G]CCTCTTTGGGGGCTA | 4666 |
rs747452504 | snp | C/T | 1.67186e-05 | 0.0028912 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721096 | CTCTTCTGAACTGAG[C/T]GGGGAGCCAGGGCAA | 4666 |
rs747530255 | snp | A/G | 5.50282e-05 | 0.0052451 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715906 | GGTTGCTTGGCAGAG[A/G]GGGTTGGGACAGGGA | 4666 |
rs747540797 | snp | G/T | 1.66355e-05 | 0.002884 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720979 | TTAAGATTAGTCTTT[G/T]GTTCTGAGGGAGCAA | 4666 |
rs747556754 | snp | A/G | 3.9405e-05 | 0.00443857 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718282 | GGAGGAGTCGCAGCT[A/G]GGGGAGTGGGGGCCC | 4666 |
rs747563973 | snp | C/G | 3.91451e-05 | 0.00442391 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718337 | CTCCTTTTGGGGAGG[C/G]AAGAGTTGCAGCTGG | 4666 |
rs747575416 | in-del | -/T | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718110 | TGGGGGTGGGGTAGC[-/T]AGACCTCCTTTTGGG | 4666 |
rs747618097 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | NACA | GRCh38.p7 | 12:56714711 | AGAAACAACTTTTAC[C/T]GCTTTATAGTAGAAA | 4666 |
rs747646922 | snp | A/G | 2.09584e-05 | 0.00323709 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717365 | CTGGTCCTCTTTTGG[A/G]GGAGGGAGGAGTCAT | 4666 |
rs747651928 | snp | C/T | 1.98222e-05 | 0.00314813 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717495 | TGGGAGAGTAGGGGT[C/T]CCTTTAGGGGAGGGA | 4666 |
rs747699874 | snp | C/G | 1.66416e-05 | 0.00288453 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716306 | TTGAAGAGTCTTTCT[C/G]AACAGGGAGTAGAGG | 4666 |
rs747745595 | snp | C/T | 1.75557e-05 | 0.00296269 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719189 | TTCCTTTGGAAGATG[C/T]AGTAGCAGAAGCACC | 4666 |
rs747789693 | snp | C/T | 1.66297e-05 | 0.0028835 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716396 | ATATAGGAGGTGAAG[C/T]AGCAGAACTCTTTTT | 4666 |
rs747808496 | in-del | -/C | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716483 | GGGCAACAAGTACTT[-/C]TTTCAGAGCTGTGGG | 4666 |
rs747831856 | snp | C/T | 1.6691e-05 | 0.00288881 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720371 | TTATGCTAGAGATGG[C/T]AGAGGGACCTTTGTC | 4666 |
rs747835618 | snp | A/C | 3.45375e-05 | 0.00415543 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719092 | TCAGGGCCAGCAGAA[A/C]CCTTCTTGGTTGGAG | 4666 |
rs747870209 | snp | A/G | 1.97307e-05 | 0.00314085 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721444 | ACACTCAAGGCTGAA[A/G]ACATAGGTAGCACAG | 4666 |
rs747873657 | snp | A/T | 1.65581e-05 | 0.00287728 | intron-variant | NACA | GRCh38.p7 | 12:56714318 | ACAGTTCCACTCTGT[A/T]TAAAGGTGCTTCATA | 4666 |
rs747919109 | snp | C/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56716036 | CATCAGCAGGGGCAA[C/G]GGGTTTAGAGGGTGA | 4666 |
rs747936397 | snp | C/G/T | 0.000133028 | 0.00815463 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720267 | AGGATAATGATAAGT[C/G/T]GCATTAGGAGAGCTT | 4666 |
rs747961735 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | NACA | GRCh38.p7 | 12:56714451 | CCAGCTAAGAAGATA[A/G]AACAGCTATTAGTTA | 4666 |
rs748003990 | snp | C/G | 1.96115e-05 | 0.00313135 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717890 | TGGGGGCCCCTTTGG[C/G]GGATGGGGTAGCTAG | 4666 |
rs748062143 | in-del | -/A | 1.70895e-05 | 0.00292309 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56721319 | TCGAGGCAATAGTAG[-/A]GGGGGAAGGGAATGG | 4666 |
rs748093948 | snp | C/T | 5.86964e-05 | 0.00541708 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717971 | TGGGGGATGGGGTAG[C/T]TAGACCTCCTTTTGG | 4666 |
rs748115761 | snp | A/G | 1.80458e-05 | 0.00300376 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715997 | AGATTGGTTCCGGGG[A/G]AATCAGAGGCAGCAG | 4666 |
rs748135618 | in-del | -/AG | 1.66457e-05 | 0.00288489 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719637 | GAGAAGCGGACCAGC[-/AG]AGTCTGGGCCTGCAT | 4666 |
rs748155577 | snp | C/G | 1.66446e-05 | 0.00288479 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719698 | GAGTTAACACCCAGA[C/G]GGGAGGTCATACTGC | 4666 |
rs748162826 | snp | C/G | 8.32425e-05 | 0.00645091 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719612 | CTGTTGGGGTAATGA[C/G]AGAACTTTTGAGAAG | 4666 |
rs748250696 | snp | C/T | 1.66427e-05 | 0.00288462 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720722 | CAGCAGGTGGACTAA[C/T]AGGCCCCTTCAGGCT | 4666 |
rs748282996 | snp | A/G | 0.000330389 | 0.0128486 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718433 | CAGCTGGGGGTGTGG[A/G]TGCCCCTTTGGGGAA | 4666 |
rs748292801 | snp | C/T | 0.000254201 | 0.011271 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716076 | CAGCCCAGGAGAGGA[C/T]GGCAGAAATTGCTGT | 4666 |
rs748366988 | in-del | -/A | 1.65556e-05 | 0.00287707 | intron-variant | NACA | GRCh38.p7 | 12:56714320 | AGTTCCACTCTGTAT[-/A]AAGGTGCTTCATAAG | 4666 |
rs748372955 | snp | A/G | 1.95804e-05 | 0.00312887 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718505 | CAGCTGGGGGTGTGG[A/G]GGCCCCTTTGGGGGA | 4666 |
rs748387766 | snp | C/T | 1.6569e-05 | 0.00287824 | synonymous-codon | NACA | GRCh38.p7 | 12:56713146 | ACCTTGAACTTTGAA[C/T]TTCTCAGCAGCTGCT | 4666 |
rs748406951 | snp | A/G | 1.97097e-05 | 0.00313918 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717601 | GCAGCTGGAGGAGTG[A/G]GGGCCCCTTTGGGGG | 4666 |
rs748410288 | snp | A/G | 1.95819e-05 | 0.00312899 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717645 | GCCTCCTTTTGGAGA[A/G]GGAGGAGTTACAACT | 4666 |
rs748427349 | snp | G/T | 1.66838e-05 | 0.00288818 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720670 | GTCTTTTGAGAAGAG[G/T]TCACCACAGGAAGAG | 4666 |
rs748498220 | snp | A/G | 3.71423e-05 | 0.00430926 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716669 | TTTCGGGGGATGGAG[A/G]AGTCACAGCTGGAGG | 4666 |
rs748502679 | snp | A/C | | | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712727 | TAGCAAGACAAAATA[A/C]AGTCACTCATAATTG | 4666 |
rs748505605 | snp | G/T | 5.19233e-05 | 0.00509499 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718970 | GAGGAGTGGGAGAAT[G/T]CGTCGTGGCTGGTGA | 4666 |
rs748533974 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725735 | GCTGCTGGACCCTCT[-/C]CCCCCCCCATCAACA | 4666 |
rs748549153 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726688 | AGCGATTCTCCTGCC[C/T]CAGCCTCCCGGGTAG | 4666 |
rs748587037 | snp | C/T | 1.97658e-05 | 0.00314364 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717706 | GTAGCTAGACCTCCT[C/T]TTAGGGAGGGAGGAG | 4666 |
rs748595708 | snp | A/G | 1.66288e-05 | 0.00288343 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720097 | AAGGCAGCAGGGGAA[A/G]TTGGTTCTATGTTAC | 4666 |
rs748685514 | snp | C/T | 4.98857e-05 | 0.00499403 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720021 | AGGAGGAGAGACTGG[C/T]ATCCTCAGAGTGGTT | 4666 |
rs748796394 | snp | A/G | 3.94073e-05 | 0.00443871 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718249 | GGGGATGGGGTAGCT[A/G]GGCCTCCTTTTGGGG | 4666 |
rs748845154 | snp | A/G | 1.94358e-05 | 0.00311729 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717274 | CCTTCTCTGGTGACT[A/G]GAGTTGCTGGAGCCT | 4666 |
rs748861315 | snp | A/G | 1.66454e-05 | 0.00288486 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721015 | GCTGACAGAGTTATC[A/G]CTGACCCTGACTCAG | 4666 |
rs748884842 | snp | A/C | 3.29506e-05 | 0.00405884 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712750 | CATAATTGGTCAGGG[A/C]AGAGGGAGTCAAGGA | 4666 |
rs748909499 | in-del | -/TT | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726287 | GGGCACTTCTTGGAT[-/TT]TTTTTTTTTTTTTTT | 4666 |
rs748931281 | snp | C/T | 7.10947e-05 | 0.00596174 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719336 | GTGAGGGCACAGACT[C/T]TGGGATTTCAGGGGC | 4666 |
rs748931864 | in-del | -/CTTTTGGGG | 3.96361e-05 | 0.00445157 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718118 | GGGTAGCTAGACCTC[-/CTTTTGGGG]AGGGAGGAGTTGCAG | 4666 |
rs748934762 | snp | A/G | 2.05273e-05 | 0.00320363 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717345 | CCCTTTGGGAGATGG[A/G]ATAGCTGGTCCTCTT | 4666 |
rs748987094 | in-del | -/CA | 1.97787e-05 | 0.00314467 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717805 | TTGCAGCTGGGGTTG[-/CA]TGGGGGCCCCTTTGG | 4666 |
rs749020893 | snp | A/G | 1.66765e-05 | 0.00288756 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716258 | CCAAGGGGCCCTTTG[A/G]GGAATGAGAAGCATC | 4666 |
rs749094834 | snp | A/G | 1.76711e-05 | 0.00297241 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719236 | CACTCTTTGGGAGAG[A/G]AAGCAACAGGTGCCA | 4666 |
rs749135715 | snp | A/T | 3.31252e-05 | 0.00406958 | intron-variant | NACA | GRCh38.p7 | 12:56713533 | CCAAGAAAAGTTTAC[A/T]CACCTTGGCTTCCCC | 4666 |
rs749155145 | snp | C/G | 3.33356e-05 | 0.00408248 | intron-variant | NACA | GRCh38.p7 | 12:56713724 | TTTTCAACCTCTTTA[C/G]AAGCAGCCTAAAGAA | 4666 |
rs749156547 | snp | A/G | 0.000220886 | 0.0105069 | intron-variant | NACA | GRCh38.p7 | 12:56724438 | TTAATGGCAAGGAGG[A/G]TAGGGAAACCTACCT | 4666 |
rs749160655 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56723434 | TACTGAAATTACAGA[A/C]TCTTTAGAGAACAGT | 4666 |
rs749182340 | snp | G/T | 1.67094e-05 | 0.0028904 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720381 | GATGGTAGAGGGACC[G/T]TTGTCAACAGATGGA | 4666 |
rs749184684 | snp | A/G/T | 0.000157585 | 0.00887531 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717808 | GCAGCTGGGGTTGTG[A/G/T]GGGCCCCTTTGGGGG | 4666 |
rs749242616 | snp | A/G/T | 4.00298e-05 | 0.00447366 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721451 | AGGCTGAAGACATAG[A/G/T]TAGCACAGCTGGAGA | 4666 |
rs749256428 | in-del | -/GGAGTCCCTTT | 1.75551e-05 | 0.00296264 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716620 | ACAGGTGGGGAAGTG[-/GGAGTCCCTTT]GGGGGCTGGAGTTGC | 4666 |
rs749274652 | snp | C/G | 0.000311696 | 0.01248 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716919 | TAGAGTTGCTGGGGT[C/G]TTTTTAGAGAGAAGA | 4666 |
rs749330898 | snp | A/G | 1.96385e-05 | 0.0031335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717859 | TTTGGGGAGGGAGGA[A/G]TTGCAGCTGGGGTTG | 4666 |
rs749416854 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715062 | AAGTTCTGTCAGAAG[A/G]TGCCCCCAGATACAC | 4666 |
rs749426278 | snp | A/C/T | 3.87449e-05 | 0.00440127 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717030 | CAGAGTGGGGGCCCC[A/C/T]ATGGGGGCTGGAGTT | 4666 |
rs749462040 | snp | C/T | 1.66443e-05 | 0.00288477 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719751 | AGGCTCCCCAAGGCT[C/T]TTCTTTGCTAGGGTG | 4666 |
rs749534808 | snp | G/T | 3.91573e-05 | 0.00442461 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718355 | GAGTTGCAGCTGGGG[G/T]TGTGGGGGCCCCTTT | 4666 |
rs749545806 | snp | A/G | 1.70179e-05 | 0.00291696 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716063 | GTGATTCCAACACCA[A/G]CCCAGGAGAGGACGG | 4666 |
rs749549995 | snp | C/T | 3.32901e-05 | 0.0040797 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719628 | AGAACTTTTGAGAAG[C/T]GGACCAGCAGAGTCT | 4666 |
rs749572084 | snp | C/T | 1.94448e-05 | 0.00311802 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718418 | GGGAGGGAGGAGTTG[C/T]AGCTGGGGGTGTGGA | 4666 |
rs749643346 | snp | A/G | 1.66286e-05 | 0.0028834 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720750 | GCTGAGGCTTCCTGG[A/G]TTTTGTGGAGAAATC | 4666 |
rs749671400 | snp | G/T | 1.64762e-05 | 0.00287016 | intron-variant | NACA | GRCh38.p7 | 12:56712915 | TTCATCGACCTGAGA[G/T]ATGAGAGGGAAAAAG | 4666 |
rs749694057 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725778 | CCCATTTTAAAACTT[C/G]AGAGATGTGATGGGT | 4666 |
rs749714859 | snp | A/G | 3.95601e-05 | 0.0044473 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717576 | GCTTCCTTTTGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs749742624 | snp | A/T | 1.7238e-05 | 0.00293576 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719061 | AACAGGGGATGAGAG[A/T]TTTCCAATAGGAGTA | 4666 |
rs749785119 | in-del | -/C | 3.29707e-05 | 0.00406008 | intron-variant | NACA | GRCh38.p7 | 12:56714555 | AAAAGTTGCCCTGAT[-/C]AACCCTGCTTCTTTG | 4666 |
rs749793112 | snp | A/G | 1.66286e-05 | 0.0028834 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720234 | TCCAACAGAAGAAAC[A/G]GGCATTTGGGCCACT | 4666 |
rs749804780 | snp | G/T | 5.88969e-05 | 0.00542632 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717625 | TTGGGGGGTGAGGTA[G/T]CTGGGCCTCCTTTTG | 4666 |
rs749806947 | snp | C/T | 1.68417e-05 | 0.00290182 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716556 | GGCCCCCATTTTACA[C/T]GTGACAGAAGCTGGG | 4666 |
rs749841226 | in-del | -/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727334 | ACGACTGTGGCCACC[-/T]TTTTTTTTTTTTTTT | 4666 |
rs749853428 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724821 | CCTCCACTCCTAATA[C/T]TCACACTGGCTGGGC | 4666 |
rs749881605 | snp | A/G | 5.14699e-05 | 0.0050727 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721323 | GGCAATAGTAGAGGG[A/G]GAAGGGAATGGGGAA | 4666 |
rs749894653 | snp | C/G | 7.83976e-05 | 0.0062604 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717694 | TTGTGGGGTGGGGTA[C/G]CTAGACCTCCTTTTA | 4666 |
rs749959670 | in-del | -/TTG | | | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56715873 | CCAAGGCAAATACCC[-/TTG]TTGTTCTTCGTAACA | 4666 |
rs749980474 | snp | A/C | 1.96953e-05 | 0.00313804 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716780 | TGGAAGGAGTCACTG[A/C]TGGGGGACTGGAGGC | 4666 |
rs750030420 | snp | C/T | 1.66449e-05 | 0.00288482 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719679 | CTTGATTACAGAGGC[C/T]GAGGAGTTAACACCC | 4666 |
rs750064901 | snp | C/T | 1.84769e-05 | 0.00303943 | intron-variant | NACA | GRCh38.p7 | 12:56715825 | AGCGCCCAAGAGGGG[C/T]GTGGACGACAGACAC | 4666 |
rs750074712 | snp | C/G | 1.96427e-05 | 0.00313384 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716867 | TTTTAGGGGAGGGAA[C/G]AGTCATAGCTGGGGG | 4666 |
rs750134059 | snp | A/T | 3.33161e-05 | 0.00408129 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719578 | GCAGGGTCAGCACTT[A/T]CCAAAGGAAATGCAG | 4666 |
rs750162555 | snp | C/T | 3.67498e-05 | 0.00428644 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715884 | ACCCTTGTTGTTCTT[C/T]GTAACAGGTTGCTTG | 4666 |
rs750167821 | snp | A/G | 7.88239e-05 | 0.0062774 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718242 | CCCTTTGGGGGATGG[A/G]GTAGCTGGGCCTCCT | 4666 |
rs750206268 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726730 | GGCATGCGCCACCAC[A/G]CCAGTCTATTTTTTG | 4666 |
rs750209011 | snp | A/C/G | 4.99882e-05 | 0.0049992 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720705 | AGTTGAAAGAGATAA[A/C/G]GCAGCAGGTGGACTA | 4666 |
rs750306017 | snp | C/T | 3.65584e-05 | 0.00427526 | intron-variant | NACA | GRCh38.p7 | 12:56724423 | TAGGGTTAATTTTAA[C/T]TAATGGCAAGGAGGG | 4666 |
rs750338709 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712555 | ACATTGTTAATTCCT[A/G]TAACAGAGAAAAGAT | 4666 |
rs750346259 | snp | A/G | 3.4395e-05 | 0.00414684 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719013 | TTGGAAAGAAAGACT[A/G]TTCTCTGGAAGAAAT | 4666 |
rs750347006 | in-del | -/AA | 4.98389e-05 | 0.00499169 | intron-variant | NACA | GRCh38.p7 | 12:56713523 | GGAACAATGCCCAAG[-/AA]AAGTTTACTCACCTT | 4666 |
rs750449840 | in-del | -/GTGGGGT | 1.97932e-05 | 0.00314582 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718100 | GGGCCCCTTTTGGGG[-/GTGGGGT]AGCTAGACCTCCTTT | 4666 |
rs750511564 | snp | A/G | 1.66286e-05 | 0.0028834 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720064 | GAAGGCTCTTTGGGA[A/G]CCACAGGTGCCATAA | 4666 |
rs750553482 | snp | C/G | 1.66294e-05 | 0.00288347 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719987 | TGGGGAGATTTTTGA[C/G]GTCTTCAGGGTCTGG | 4666 |
rs750602280 | snp | G/T | 3.92881e-05 | 0.00443199 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717848 | CCAGACCTCCTTTTG[G/T]GGAGGGAGGAGTTGC | 4666 |
rs750605146 | snp | A/G | 1.67083e-05 | 0.00289031 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721174 | GCTATCATGGGAGAG[A/G]CTAGAGCTAAGGCAG | 4666 |
rs750642352 | snp | A/G | 0.000166945 | 0.0091348 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721079 | TAGGTGGAAAAGCAG[A/G]ACTCTTCTGAACTGA | 4666 |
rs750678032 | in-del | -/GTTGC | 6.08865e-05 | 0.0055172 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718135 | TTTGGGGAGGGAGGA[-/GTTGC]AGCTGGGGTTGTGGG | 4666 |
rs750725086 | snp | C/T | 1.93721e-05 | 0.00311219 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717012 | AGAAGGAATCACAGC[C/T]GGCAGAGTGGGGGCC | 4666 |
rs750756822 | snp | A/G | 1.73779e-05 | 0.00294765 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719391 | ACAGGTATTCTGGGG[A/G]GATGGAGCCACAGGG | 4666 |
rs750990169 | snp | C/T | 0.000140233 | 0.00837238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718945 | GGAGTAGGGGCCCCT[C/T]TGGGGGATGGAGGAG | 4666 |
rs751009393 | snp | C/G | 3.37781e-05 | 0.00410949 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720478 | ACAGATCTCTGAGAA[C/G]GATAAGAGGCCCCTG | 4666 |
rs751060274 | snp | A/G | 3.90213e-05 | 0.00441692 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718481 | TTCCTTTGGGGGAGG[A/G]AGGAGTCACAGCTGG | 4666 |
rs751101088 | snp | A/G | 1.66704e-05 | 0.00288703 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720354 | GCCAGAAGGGCTGCA[A/G]GTTATGCTAGAGATG | 4666 |
rs751152080 | snp | A/G | 1.96381e-05 | 0.00313347 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717621 | CCCTTTGGGGGGTGA[A/G]GTAGCTGGGCCTCCT | 4666 |
rs751193219 | snp | C/T | 3.8276e-05 | 0.00437454 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721416 | AGGTCCAGGCTGCCC[C/T]AAGGCAGCAGTGACA | 4666 |
rs751196720 | in-del | -/AG | 1.66949e-05 | 0.00288915 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56721077 | GTTAGGTGGAAAAGC[-/AG]AACTCTTCTGAACTG | 4666 |
rs751207900 | in-del | -/CAA | | | upstream-variant-2KB, cds-indel | NACA | GRCh38.p7 | 12:56725746 | CCTCTCCCCCCCCAT[-/CAA]CAACAACAAAAAAAC | 4666 |
rs751241903 | snp | C/T | 3.91382e-05 | 0.00442352 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717678 | GGGATTGGGGGCCCC[C/T]TTGTGGGGTGGGGTA | 4666 |
rs751245633 | snp | G/T | 1.95513e-05 | 0.00312654 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56716760 | GGATGGGGCCCCTTT[G/T]TAAGTGGAAGGAGTC | 4666 |
rs751331469 | snp | A/G | 1.67562e-05 | 0.00289444 | intron-variant | NACA | GRCh38.p7 | 12:56714731 | TATAGTAGAAATTAT[A/G]AGAGAAGGTACTTCA | 4666 |
rs751342409 | in-del | -/CT | 4.9831e-05 | 0.00499129 | intron-variant | NACA | GRCh38.p7 | 12:56713717 | TATCAGGTTTTCAAC[-/CT]CTTTAGAAGCAGCCT | 4666 |
rs751352879 | snp | A/G | 3.32862e-05 | 0.00407946 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719685 | TACAGAGGCCGAGGA[A/G]TTAACACCCAGAGGG | 4666 |
rs751353926 | snp | A/G | 3.93871e-05 | 0.00443757 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718084 | GCAGCTGGGGTTGTG[A/G]GGGCCCCTTTTGGGG | 4666 |
rs751396991 | snp | C/T | 1.66272e-05 | 0.00288328 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720821 | CGATGGCTAGGGTAG[C/T]TGTGGGTGTTGTCTG | 4666 |
rs751415216 | snp | A/G | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712326 | ACTAAACCTTATCAA[A/G]TGAGGGAGGCCTTAG | 4666 |
rs751482228 | snp | C/T | 1.83981e-05 | 0.00303294 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715871 | AACCAAGGCAAATAC[C/T]CTTGTTGTTCTTCGT | 4666 |
rs751504854 | snp | A/G | 1.97101e-05 | 0.00313921 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718236 | GGGGGCCCCTTTGGG[A/G]GATGGGGTAGCTGGG | 4666 |
rs751509908 | in-del | -/AGGAGTTACAA | 1.91168e-05 | 0.00309161 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717178 | GGCCTCCTTTGGGGG[-/AGGAGTTACAA]CTGAAGTTGCTGGGG | 4666 |
rs751531571 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56713818 | GAATAGAGAATGGGT[C/T]TTCTGCCGTAGTAAC | 4666 |
rs751547798 | snp | A/G | 1.66557e-05 | 0.00288575 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720711 | AAGAGATAAGGCAGC[A/G]GGTGGACTAACAGGC | 4666 |
rs751562955 | in-del | -/GGA | 1.68103e-05 | 0.00289911 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56716136 | GCAAGAGGCAGAGAG[-/GGA]ACTGGTGGGGAGGGT | 4666 |
rs751593175 | snp | A/G | 2.00282e-05 | 0.00316445 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717317 | GAGGAATCACTGCTG[A/G]GGAAGTGGGGTCCCC | 4666 |
rs751595415 | in-del | -/T | 1.87929e-05 | 0.00306531 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718709 | TTGCAGCTGGGGGTG[-/T]GGGGGCCCCTTTGGG | 4666 |
rs751620181 | snp | C/T | 2.04342e-05 | 0.00319636 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717434 | GAGTGGGGCCCTCTT[C/T]GGAGGATGGAGTAGT | 4666 |
rs751683482 | snp | C/G | 1.73794e-05 | 0.00294778 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718955 | CCCCTTTGGGGGATG[C/G]AGGAGTGGGAGAATG | 4666 |
rs751756445 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720171 | CTCAAAGGTAGTAGT[A/G]GGTGCTGCAGCAATT | 4666 |
rs751806934 | snp | C/G/T | 3.32675e-05 | 0.00407834 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716343 | AGCCACTGTGGAAAG[C/G/T]GGTCCTTTAGAACCA | 4666 |
rs751815629 | snp | C/T | 5.09714e-05 | 0.00504808 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721305 | AACTTCTAAAGGGGT[C/T]GAGGCAATAGTAGAG | 4666 |
rs751868352 | snp | A/G | 0.000166217 | 0.00911486 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717788 | CTTTTGGGGAGGGAG[A/G]AGTTGCAGCTGGGGT | 4666 |
rs751896200 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | NACA | GRCh38.p7 | 12:56713668 | TAACCTGCCGAAGAC[C/T]CAGTTTGGACATAGC | 4666 |
rs751905506 | snp | A/G | 1.67044e-05 | 0.00288997 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721184 | GAGAGGCTAGAGCTA[A/G]GGCAGCTGGGGAGAT | 4666 |
rs751956454 | snp | A/G | 5.89837e-05 | 0.00543032 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717835 | GGGGATGGGGTAGCC[A/G]GACCTCCTTTTGGGG | 4666 |
rs751984054 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | NACA | GRCh38.p7 | 12:56714408 | TTTGCTTTACTGACT[A/G]GTTCTTCATCAATTT | 4666 |
rs752002923 | in-del | -/GGGTTGTGGGTGCCCCTTTGT | 3.4562e-05 | 0.0041569 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718145 | GAGGAGTTGCAGCTG[-/GGGTTGTGGGTGCCCCTTTGT]GGGGTGGGGTAGCTA | 4666 |
rs752074572 | snp | A/G | 1.82904e-05 | 0.00302405 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715970 | GGACCGACTGGAAAG[A/G]CACTCCCCCAGAGAT | 4666 |
rs752106502 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715766 | CCAAACCCAAGCAGA[C/T]TCACTGGAGAAAGCG | 4666 |
rs752159836 | snp | A/T | 1.72767e-05 | 0.00293905 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719403 | GGGGGATGGAGCCAC[A/T]GGGCAATTTTCTGAA | 4666 |
rs752229873 | snp | C/T | 2.38121e-05 | 0.00345043 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724538 | TCTGAAGGAAGGGAA[C/T]AAAAAGGAGGCCTAA | 4666 |
rs752249949 | snp | A/C | 1.77801e-05 | 0.00298157 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719329 | AGAGAGGGTGAGGGC[A/C]CAGACTTTGGGATTT | 4666 |
rs752250041 | snp | C/G | 3.33634e-05 | 0.00408418 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720615 | TGCAAGATGAGAGCC[C/G]AGAGAAATGGGAAAA | 4666 |
rs752271026 | snp | A/G | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724530 | CGGGCATTTCTGAAG[A/G]AAGGGAATAAAAAGG | 4666 |
rs752337847 | snp | A/G | 1.68786e-05 | 0.002905 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720486 | CTGAGAAGGATAAGA[A/G]GCCCCTGTGGAAGAA | 4666 |
rs752373005 | in-del | -/TCC | 4.15373e-05 | 0.00455707 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717354 | AGATGGGATAGCTGG[-/TCC]TCTTTTGGGGGAGGG | 4666 |
rs752381805 | snp | A/G | 0.000178294 | 0.00944008 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717559 | GGGGGTGGGGTACCT[A/G]GGCTTCCTTTTGGGG | 4666 |
rs752386935 | snp | C/G | 1.94222e-05 | 0.0031162 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718451 | CCCCTTTGGGGAATG[C/G]GGTAGCTGCTGGACT | 4666 |
rs752392098 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56721054 | ACTGAAGGAGGTGAA[A/G]TAAGAAGGTTAGGTG | 4666 |
rs752422558 | snp | C/G | 3.52703e-05 | 0.00419927 | intron-variant | NACA | GRCh38.p7 | 12:56724429 | TAATTTTAATTAATG[C/G]CAAGGAGGGTAGGGA | 4666 |
rs752423047 | snp | C/T | 1.6661e-05 | 0.00288621 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716495 | CTTCTTTCAGAGCTG[C/T]GGGGCCTTTCTTTGC | 4666 |
rs752449057 | snp | C/T | 3.50785e-05 | 0.00418784 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718810 | GATAGAGCAGGAGCC[C/T]GTTTGGGTGCTGGAG | 4666 |
rs752512727 | snp | A/C | 1.73096e-05 | 0.00294185 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716604 | GAGGGAGGAAGGAGT[A/C]ACAGGTGGGGAAGTG | 4666 |