SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs724125 | snp | A/G | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112551459 | CCAGGAATTTAGCCA[A/G]AAGTGTGGACACTGA | 64422 |
rs923695 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ATG3 | GRCh38.p7 | 3:112540650 | AAAAAAAGAAACCCA[C/T]GGAACAGTAACATTT | 64422 |
rs958935 | snp | A/G | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112551565 | CTAGTACCTGCTAAA[A/G]AAAGATCCCGTCCAT | 64422 |
rs971832 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | ATG3 | GRCh38.p7 | 3:112553800 | ACTTTATTATATCAC[A/T]GGGCACACTTCTTCC | 64422 |
rs1388442 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ATG3 | GRCh38.p7 | 3:112538444 | CACAAGCCTACTTCT[A/G]TAACTGCGTAgtcat | 64422 |
rs1491629 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ATG3 | GRCh38.p7 | 3:112539775 | ATACCATTAACACAA[C/T]TGTTGAGCAAAATTA | 64422 |
rs1873571 | snp | G/T | 0.407158 | 0.194426 | intron-variant | ATG3 | GRCh38.p7 | 3:112540541 | GGATGTAATTTATAC[G/T]CTATCTTTCTTGTTG | 64422 |
rs1873572 | snp | A/G | 0.326741 | 0.23793 | intron-variant | ATG3 | GRCh38.p7 | 3:112540762 | AGAAACCAAGAGAGA[A/G]AAAAAAAAGAGGAAG | 64422 |
rs2035830 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ATG3 | GRCh38.p7 | 3:112544497 | cgtttctactaaaaa[A/C/T]acaaaagttagctca | 64422 |
rs2279532 | snp | A/G | 0.445855 | 0.155373 | intron-variant, upstream-variant-2KB | ATG3, SLC35A5 | GRCh38.p7 | 3:112561371 | ACACCTTGCCCCGCC[A/G]GAGAAAGCGGGGACT | 64422 |
rs2399431 | snp | C/G | 0.0498117 | 0.149749 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112561859 | ACCCCTCGCCCTCTG[C/G]GAGCTGTCTGTCCTC | 64422 |
rs2638016 | snp | A/G | 0.42357 | 0.179927 | intron-variant | ATG3 | GRCh38.p7 | 3:112539396 | TTACATAAGCCAAAC[A/G]TGTTCCCACCTCAGT | 64422 |
rs2638017 | snp | C/T | 0.408359 | 0.193449 | intron-variant | ATG3 | GRCh38.p7 | 3:112540311 | CATCACTTGCCATTA[C/T]GGTGTTTCAACTCTA | 64422 |
rs2638018 | snp | A/G | 0.40733 | 0.194287 | intron-variant | ATG3 | GRCh38.p7 | 3:112541185 | tgaggttaagagatc[A/G]agaccatcctggcca | 64422 |
rs2638019 | snp | C/T | 0.321769 | 0.239477 | intron-variant | ATG3 | GRCh38.p7 | 3:112543363 | TGAGAAATGAAAAGC[C/T]AATCTAATACCTACA | 64422 |
rs2638020 | snp | C/T | 0 | 0 | intron-variant | ATG3 | GRCh38.p7 | 3:112545276 | TCAAAACCTACTTGT[C/T]TCAAAGAAAGCCTTA | 64422 |
rs2638021 | snp | G/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112546456 | tgctactcccaacag[G/T]ggggacaaaaattaa | 64422 |
rs2638022 | snp | C/T | 0.423881 | 0.179625 | intron-variant | ATG3 | GRCh38.p7 | 3:112546929 | ATAGCACTCGACTCA[C/T]TAATAAGCCAATAAA | 64422 |
rs2638023 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ATG3 | GRCh38.p7 | 3:112547615 | CAAAACAGTGTTTTA[A/G]GACTTAGAATAAAAA | 64422 |
rs2638024 | snp | A/G | | | intron-variant | ATG3 | GRCh38.p7 | 3:112548011 | GTATTTAGAAACTAA[A/G]AAAATAATATTTTCA | 64422 |
rs2638025 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | ATG3 | GRCh38.p7 | 3:112550901 | CTCTAAACAGTAGAA[A/C]ATATAAATATCCCAT | 64422 |
rs2638026 | snp | A/T | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112552366 | TGTGAAAACTGCTAA[A/T]TTGCTTAAGGTACCT | 64422 |
rs2638027 | snp | A/T | 0.331411 | 0.236373 | intron-variant | ATG3 | GRCh38.p7 | 3:112552649 | AAAACCTGTTCAAAA[A/T]TTTTTTTTTTTTTTT | 64422 |
rs2638028 | snp | C/G | 0.332337 | 0.236052 | upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112562693 | GTCTGTCCTAATAAG[C/G]TTTTTCCTCCGAGGG | 64422 |
rs2638029 | snp | C/G | 0.334412 | 0.235318 | upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112562715 | CTCCGAGGGAAAAGA[C/G]GAGGAAAATACAATT | 64422 |
rs2638032 | snp | C/T | 0.325799 | 0.238232 | intron-variant | ATG3 | GRCh38.p7 | 3:112535854 | ACCAACCTAAAGAAA[C/T]TGGCATGTAGTAACT | 64422 |
rs2638037 | snp | A/G | 0.408359 | 0.193449 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112533543 | CTGATTAGACGTGGC[A/G]TCTTAGTCTCCACAT | 64422 |
rs2705505 | snp | A/T | 0.333491 | 0.235646 | intron-variant, upstream-variant-2KB | ATG3, SLC35A5 | GRCh38.p7 | 3:112561149 | GATTGAAGAACGTTA[A/T]ATCCAAACACTGGAA | 64422 |
rs2705507 | snp | G/T | 0.325091 | 0.238456 | intron-variant, upstream-variant-2KB | ATG3, SLC35A5 | GRCh38.p7 | 3:112560863 | CAGATAGCCGTAGCT[G/T]GTTATTAGTGATAAC | 64422 |
rs2705519 | snp | C/G | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112551835 | CTCTGATTTAATAAA[C/G]GTGGTTTTTTTTTCT | 64422 |
rs2705520 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ATG3 | GRCh38.p7 | 3:112550440 | CTTAGATTATTGTTG[C/T]GCTTTTCTCCATGCC | 64422 |
rs2705521 | snp | C/T | 0.333722 | 0.235565 | intron-variant | ATG3 | GRCh38.p7 | 3:112549909 | GGCAAATGAAATTCA[C/T]ACTACCTATGACATC | 64422 |
rs2705522 | snp | C/T | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112549863 | GACGATGTTATTATC[C/T]GTTGTGTCATTGAAG | 64422 |
rs2705523 | snp | G/T | 0.317451 | 0.240729 | intron-variant | ATG3 | GRCh38.p7 | 3:112549807 | AGTGGTTTTTTTTTT[G/T]TTTTTTTTGGTTGTT | 64422 |
rs2705527 | snp | C/T | 0.00383876 | 0.0436422 | intron-variant | ATG3 | GRCh38.p7 | 3:112558232 | GATTTATGGGAATTT[C/T]TACTTCCCATAGAAG | 64422 |
rs2705554 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ATG3 | GRCh38.p7 | 3:112554699 | TTGTTCATGGGTTTA[C/T]TACACAGCAAAAAAT | 64422 |
rs2705556 | snp | C/T | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112546627 | GCTAATAGAAGAAAA[C/T]GCCCAGGAAAAGCAA | 64422 |
rs2705557 | snp | C/G | | | intron-variant | ATG3 | GRCh38.p7 | 3:112548105 | atgcctgtaatccta[C/G]cactttgggaggccg | 64422 |
rs2705558 | snp | A/G | 0 | 0 | intron-variant | ATG3 | GRCh38.p7 | 3:112545330 | AGGTACTTTGAAGTA[A/G]AAATGTTATCTAGCT | 64422 |
rs2705559 | snp | G/T | 0.423413 | 0.180077 | intron-variant | ATG3 | GRCh38.p7 | 3:112545108 | cattattactgtaac[G/T]tcctcataagatagt | 64422 |
rs2705562 | snp | C/G | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112538606 | TTTCCTGGCTTTCCT[C/G]CCTCATCACTGAGTG | 64422 |
rs2705563 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | ATG3 | GRCh38.p7 | 3:112539277 | tgtctcactctgagt[A/T]atgtcaagaccttat | 64422 |
rs2705564 | snp | C/G | 0.332337 | 0.236052 | upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112563019 | aggctggagtgcaac[C/G]gcgcggtcttggctc | 64422 |
rs2933134 | snp | C/G | 0.333722 | 0.235565 | intron-variant | ATG3 | GRCh38.p7 | 3:112537063 | ATTCTAGACTGTTTA[C/G]AATGATTTCTGGGAA | 64422 |
rs2933140 | snp | C/T | 0.0452528 | 0.143452 | downstream-variant-500B | ATG3 | GRCh38.p7 | 3:112532025 | CTAAGCCCTTTATTC[C/T]CTTTATACCACTACA | 64422 |
rs2952324 | snp | C/G | 0.325799 | 0.238232 | intron-variant | ATG3 | GRCh38.p7 | 3:112558970 | gggtggatcacctga[C/G]gtcaggagttcgaga | 64422 |
rs2952325 | snp | A/G | 0.326035 | 0.238157 | intron-variant | ATG3 | GRCh38.p7 | 3:112549171 | TACTAGTGTGGTATA[A/G]AGAAGTAAAAATCAG | 64422 |
rs2952326 | snp | C/T | 0.40733 | 0.194287 | intron-variant | ATG3 | GRCh38.p7 | 3:112542921 | ATTGCTTTGCTGTTT[C/T]AGAAGATCTTGTTTA | 64422 |
rs2952327 | snp | C/T | 0.40733 | 0.194287 | intron-variant | ATG3 | GRCh38.p7 | 3:112542825 | AGTGTTTTTCTTGGA[C/T]GGGCTTATGGTAATT | 64422 |
rs2969895 | snp | C/T | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112548883 | AAGGAATGCATAGAA[C/T]ATTCCCAATAGAGCT | 64422 |
rs2969896 | snp | C/T | 0.174773 | 0.238413 | synonymous-codon | ATG3 | GRCh38.p7 | 3:112537783 | CCTTTACATCACTTA[C/T]GATAAATATTACCAG | 64422 |
rs3083210 | in-del | -/ATG/TGA | 0.21875 | 0.248039 | intron-variant | ATG3 | GRCh38.p7 | 3:112536144 | ACCATATCTAAATGA[-/ATG/TGA]CTATTTCTGAGTCAA | 64422 |
rs3109033 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ATG3 | GRCh38.p7 | 3:112536863 | CGCAATCTCAGCTCA[C/T]TGCAAGCTCTGCCTC | 64422 |
rs3732817 | snp | C/T | 0.397271 | 0.202018 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112533685 | ATCCTAAAGTACATG[C/T]ACTCATAGCATAGAT | 64422 |
rs3736269 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | ATG3 | GRCh38.p7 | 3:112541724 | TTACAACTCAATGAA[A/G]AATTCTTAATCCACA | 64422 |
rs3736270 | snp | A/C | 0.125146 | 0.21659 | intron-variant | ATG3 | GRCh38.p7 | 3:112544012 | ATAGATAGATAGGCA[A/C]ATAACTACTCATTAA | 64422 |
rs3736271 | snp | C/T | 0.122431 | 0.215003 | intron-variant | ATG3 | GRCh38.p7 | 3:112544110 | TTCCTGTAATACCTA[C/T]GTAAAATTCGGCAGA | 64422 |
rs3755745 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG3, SLC35A5 | GRCh38.p7 | 3:112560453 | GGAAGTACTAGGTCT[A/G]TACTTTTTAAAATAC | 64422 |
rs4682110 | snp | A/G | 0.393987 | 0.204372 | intron-variant | ATG3 | GRCh38.p7 | 3:112534909 | AAGAAAAGCTAATTG[A/G]TTAGAGTTGAGAGGT | 64422 |
rs5000995 | snp | C/T | 0.440884 | 0.161442 | intron-variant | ATG3 | GRCh38.p7 | 3:112551378 | GATAGCACTTGTGCA[C/T]GTGAAGGCATAAGCA | 64422 |
rs5851841 | in-del | -/ATG | 0.039522 | 0.134904 | intron-variant | ATG3 | GRCh38.p7 | 3:112536143 | GCAAACCATATCTAA[-/ATG]ATGACTATTTCTGAG | 64422 |
rs6767088 | snp | G/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112548785 | TTTAAAGGTGATTAA[G/T]AGTTACATTCAGCTC | 64422 |
rs6792947 | snp | A/C | 0.44252 | 0.159487 | intron-variant | ATG3 | GRCh38.p7 | 3:112554064 | GGGAGATAAACTTTA[A/C]CCATTTGAGAATTAT | 64422 |
rs7372758 | snp | A/C | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556493 | ggaagtgaggagccc[A/C]tctgcccggccacca | 64422 |
rs7372782 | snp | C/T | 0.120326 | 0.21374 | intron-variant | ATG3 | GRCh38.p7 | 3:112556860 | atcaccactccctaa[C/T]ctcaagtacccaggg | 64422 |
rs7373654 | snp | G/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556653 | gaaagaggtagacat[G/T]gtagacttttcattt | 64422 |
rs7373655 | snp | G/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556655 | aagaggtagacattg[G/T]agacttttcattttg | 64422 |
rs7374457 | snp | A/C | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556763 | acatgtgctgtgtcc[A/C]ctcagggttgaatgg | 64422 |
rs7374469 | snp | A/G | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556897 | acactgcggaaggcc[A/G]cagggtcctctgcct | 64422 |
rs7617497 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ATG3 | GRCh38.p7 | 3:112537079 | AATGATTTCTGGGAA[A/G]TTTTACAATTTATTA | 64422 |
rs7624917 | snp | C/T | 0.0352966 | 0.128072 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112532977 | GACTACCTGACCACT[C/T]ATTCGATTATTGAAT | 64422 |
rs7625366 | snp | C/T | 0.440746 | 0.161604 | intron-variant | ATG3 | GRCh38.p7 | 3:112548422 | TTTCATGTAAGTCTA[C/T]TGGGACAAAACTATG | 64422 |
rs9713279 | snp | G/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112556914 | agggtcctctgccta[G/T]gaaaaccagagacct | 64422 |
rs9809247 | snp | A/G | 0.295619 | 0.245803 | intron-variant | ATG3 | GRCh38.p7 | 3:112548676 | ACAGTTAACTAGCAC[A/G]TAATCTGCTAACCAT | 64422 |
rs9831088 | snp | A/G | 0.395635 | 0.2032 | intron-variant | ATG3 | GRCh38.p7 | 3:112540146 | ATTTTGGTTACAAGT[A/G]ATTCATTCAGATTTC | 64422 |
rs9855848 | snp | C/T | 0.396909 | 0.202282 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112532928 | AAGAATTCAACTATG[C/T]AAATTTGTGTCTATT | 64422 |
rs10601022 | in-del | -/TTTG | 0.334412 | 0.235318 | upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112563864 | AAGTAGAAGGATATA[-/TTTG]TTTGGTCACTTGGCA | 64422 |
rs10718853 | in-del | -/A | 0.18325 | 0.240924 | intron-variant | ATG3 | GRCh38.p7 | 3:112534777 | CATATCAGGCAAATT[-/A]AAAAAAAAAAAAAAA | 64422 |
rs11361592 | in-del | -/C | | | intron-variant | ATG3 | GRCh38.p7 | 3:112549798 | CTGTCTCAAAACAAC[-/C]AAAAAAAAAAAAAAA | 64422 |
rs11381118 | in-del | -/A/AA/AAA | 0.383956 | 0.238518 | intron-variant | ATG3 | GRCh38.p7 | 3:112534346 | CAAAAAAAAAAAAAA[-/A/AA/AAA]TTGTTAATGTAGATC | 64422 |
rs11418937 | in-del | -/A | | | intron-variant | ATG3 | GRCh38.p7 | 3:112540632 | AGAGTAAGCAAGGGG[-/A]AAAAAAAAAAGAAAC | 64422 |
rs11547151 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112561549 | TCCCGTCGCGGGGCC[G/T]GCCGCTACTCCGGCC | 64422 |
rs11547152 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATG3, SLC35A5 | GRCh38.p7 | 3:112561760 | AGCTGGGTCCGGTCC[C/G]TCGCGGGCTGCCTGG | 64422 |
rs11547153 | snp | A/C | | | stop-gained | ATG3 | GRCh38.p7 | 3:112541845 | CTTCATCTTCTTCCT[A/C]TTCACATAGTGCTGA | 64422 |
rs11707075 | snp | C/T | | | intron-variant | ATG3 | GRCh38.p7 | 3:112544487 | atggtgaaaccgttt[C/T]tactaaaaatacaaa | 64422 |
rs11923995 | snp | C/G | 0.00704273 | 0.0589217 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112532827 | TGTAAATAGTTCTAT[C/G]TTTTAAGCCCATGTT | 64422 |
rs11926664 | snp | G/T | 0.00943375 | 0.0680285 | intron-variant | ATG3 | GRCh38.p7 | 3:112540098 | ATATGGAAGTCCCTA[G/T]CATACAGATGGTATG | 64422 |
rs13060790 | snp | C/T | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112534610 | CAGGGGAGGGCATAA[C/T]CTTAAAAAGCTATGG | 64422 |
rs13064534 | snp | C/T | 0.137867 | 0.223442 | intron-variant | ATG3 | GRCh38.p7 | 3:112549536 | TGTTTCagccaggcg[C/T]ggtggctcacacctg | 64422 |
rs13071492 | snp | A/C | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112545220 | AATCCATACAAGCTA[A/C]CTTTTGGTTCAATTC | 64422 |
rs13080749 | snp | C/T | 0.137187 | 0.223099 | intron-variant | ATG3 | GRCh38.p7 | 3:112534611 | AGGGGAGGGCATAAT[C/T]TTAAAAAGCTATGGT | 64422 |
rs13082005 | snp | A/G | 0.332337 | 0.236052 | intron-variant | ATG3 | GRCh38.p7 | 3:112552010 | GACAACTGTTTCAGC[A/G]ACACGGTAAGTATTA | 64422 |
rs13094649 | snp | C/G | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112547088 | AGCCCTCTGTCTACT[C/G]CAGTGAGTCTCAACT | 64422 |
rs16859716 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime, intron-variant | ATG3 | GRCh38.p7 | 3:112533601 | ACCACCAAGTCAAGT[A/G]TTAACCTAGCATCAA | 64422 |
rs16859727 | snp | A/G | 0.137867 | 0.223442 | intron-variant | ATG3 | GRCh38.p7 | 3:112535997 | CTTGCTAAGGCTGAC[A/G]AGCTCTCAACTGAAG | 64422 |
rs16859758 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | ATG3 | GRCh38.p7 | 3:112551144 | TGGAGTGGTATGTGG[C/T]GCCTTTCACAAACAT | 64422 |
rs16859775 | snp | A/G | 0.139903 | 0.224452 | intron-variant | ATG3 | GRCh38.p7 | 3:112552293 | CAGGGAGTCTTTATC[A/G]TGAGTACTTGGAAGT | 64422 |
rs16859779 | snp | A/G | 0.137527 | 0.223271 | intron-variant | ATG3 | GRCh38.p7 | 3:112553000 | AAGAACCAGAAGGTC[A/G]GACTTAGACACTATA | 64422 |
rs16859787 | snp | A/G | 0.140919 | 0.224948 | intron-variant | ATG3 | GRCh38.p7 | 3:112555766 | CTGTAATTGTGCTCT[A/G]TCCCAACCCTGCATT | 64422 |
rs16859793 | snp | C/T | 0.140581 | 0.224783 | intron-variant | ATG3 | GRCh38.p7 | 3:112557714 | CTCTAGCTCCACACC[C/T]TGGACCTTAACAGCA | 64422 |