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 |