| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs60512164 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459510 | AGTGTTTTTTTTTTT[-/TT]AAGTGATTATGTTAG | 10533 |
| rs60548708 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294589 | AAAAGCCAAAAAATA[A/T]TTAATAGGAGTTGAG | 10533 |
| rs60599857 | snp | C/T | 0.0283406 | 0.115616 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556527 | TAGCAATAACAAACT[C/T]GTGGCTATGAATGCA | 10533 |
| rs60657917 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11502398 | CCCCACAACAGTCCC[A/C]AGAGTGTGATGTTCC | 10533 |
| rs60726911 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11284528 | CTGGTATGGTTTAAA[G/T]ATAGGGGTTTTGTTC | 10533 |
| rs60756831 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | ATG7 | GRCh38.p7 | 3:11404013 | ATTTAAAAGAAATCT[C/T]CCCCCCAGATTTTTG | 10533 |
| rs60798834 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11467685 | CTGGCCCTATTTTTT[C/T]ATTCCTTTGTCCTGT | 10533 |
| rs60815384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516449 | ACACTGACAACACCG[A/G]ATGGTAGTGAGAATG | 10533 |
| rs60867741 | in-del | -/CTTGT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410384 | AATTCAGAAATTTGT[-/CTTGT]TGACAAATGTACTTT | 10533 |
| rs60873262 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11296407 | CACCAAGATACCAAG[A/T]TAGGTCACCTTTTAT | 10533 |
| rs60878265 | in-del | -/TCACCTCACAGGTAGATGTGAGG | 0.257454 | 0.249889 | intron-variant | ATG7 | GRCh38.p7 | 3:11553267 | GGCTTGTTTCCATCT[-/TCACCTCACAGGTAGATGTGAGG]TCACCTCACAGGTAG | 10533 |
| rs60927732 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286790 | AATATTTTTGGTAGA[A/G]ACGGAATGTTGCCCA | 10533 |
| rs60966861 | in-del | -/GGGGGTTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452025 | GGACTTGGGGGGTTG[-/GGGGGTTG]TGGGAGGGAAATAGG | 10533 |
| rs61074517 | in-del | -/CTAA | 0.320335 | 0.239902 | intron-variant | ATG7 | GRCh38.p7 | 3:11539518 | TGGGAAATAAGACCT[-/CTAA]CTAAATGAGTGGGAG | 10533 |
| rs61176051 | in-del | -/TTG/TTTG/TTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378045 | TTTTTTTTTTTTTTT[-/TTG/TTTG/TTTT]GAGATGGAGTCTTAC | 10533 |
| rs61275424 | snp | C/G | 0.270351 | 0.24917 | intron-variant | ATG7 | GRCh38.p7 | 3:11554111 | TGGGGGTGTCGGCCA[C/G]GGTGGCTCTTGCTGG | 10533 |
| rs61390053 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352879 | GAGGGAGGCAAGGAC[A/C]AGAGAGTGGTGGGAA | 10533 |
| rs61390929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11402844 | AGTTTATTTAACAAT[C/T]GACGTCAACAATTAC | 10533 |
| rs61479699 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | ATG7 | GRCh38.p7 | 3:11279309 | AAGAATTGTTCCATC[C/G]AGCATGCCAGTAGGG | 10533 |
| rs61529561 | in-del | -/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11314798 | AAAAAGTTAGCTGAG[-/C]CATGGTGGTGTGTGC | 10533 |
| rs61549280 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ATG7 | GRCh38.p7 | 3:11405817 | TAGAGATGGGGTTTC[A/G]CTGTGTTTCCCAGGC | 10533 |
| rs61586366 | in-del | -/A | 0.0748431 | 0.178382 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556632 | GAACAACAAAAAAAA[-/A]TGAATGATTACAATA | 10533 |
| rs61587479 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11319693 | GGCTTCATTGGCTCA[G/T]AATGATGCTGCTTCT | 10533 |
| rs61592473 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525469 | TTTTTTTTTTTTTTT[-/T]ACTCCTTTGCCCTTG | 10533 |
| rs61599058 | in-del | -/TA | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527093 | ATATATATATATATA[-/TA]CATACATATACATAT | 10533 |
| rs61645656 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11350948 | AAAAAAAAAAAAAAA[-/A]GCAGTGATCCAATCT | 10533 |
| rs61709349 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | ATG7 | GRCh38.p7 | 3:11538226 | CGTGGCAGGCTGGGT[A/G]GCACTGCCCTCTCAA | 10533 |
| rs62245861 | snp | A/G | 0.394354 | 0.204112 | intron-variant | ATG7 | GRCh38.p7 | 3:11334787 | ATATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 10533 |
| rs62245862 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337385 | TTGAACCTGGGAGGC[A/C/G]GAGGTTGCAGTGAGC | 10533 |
| rs62245864 | snp | C/T | 0.369142 | 0.219784 | intron-variant | ATG7 | GRCh38.p7 | 3:11375652 | GCAACCTCTGCCTTC[C/T]GGTTTCAAGCAATTC | 10533 |
| rs62245865 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11388453 | TTTTTTTTTTTTAAG[G/T]AGTCTTGCTCTGTTG | 10533 |
| rs62245866 | snp | G/T | 0.396364 | 0.202676 | intron-variant | ATG7 | GRCh38.p7 | 3:11392818 | GTTTTTTGTTTGTTT[G/T]GTAGAAACTGGTAAC | 10533 |
| rs62245867 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11397741 | GGATTACAGGCGTGC[A/C]CCCACGCCCAGCCCG | 10533 |
| rs62245868 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11397742 | GATTACAGGCGTGCA[A/C]CCACGCCCAGCCCGG | 10533 |
| rs62245869 | snp | A/G | 0.145642 | 0.227177 | intron-variant | ATG7 | GRCh38.p7 | 3:11398346 | TAAACAAGTTTCAAC[A/G]AATTTCAGAGTGAAA | 10533 |
| rs62245870 | snp | A/G | 0.224412 | 0.248687 | intron-variant | ATG7 | GRCh38.p7 | 3:11398364 | TTTCAGAGTGAAATT[A/G]TATAGATGTATACTG | 10533 |
| rs62245872 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406696 | TGGTGGAAGGTAAGG[A/G]GGAGCAAGTCACATC | 10533 |
| rs62245888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11413280 | CCTTCTTTCATCACT[A/G]TGTATATTTGCTGTG | 10533 |
| rs62245889 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | ATG7 | GRCh38.p7 | 3:11418167 | TGGAGTGCAATCGTG[C/T]GATCTCAGCTCACTG | 10533 |
| rs62245891 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420747 | TACCTTAAGTAATAC[A/T]AAATACTTTTTTTTT | 10533 |
| rs62245893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429925 | AATTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 10533 |
| rs62245894 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444153 | TGTGCGGCTAAAGTT[A/C]ATTTTCGTTGCTATG | 10533 |
| rs62245895 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11447468 | CAAGACTCCGTCTCA[A/G]GGAAAAAAAAAAAAA | 10533 |
| rs62245896 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451764 | TAGAAAATATTACGT[G/T]TATATATATGTTTAT | 10533 |
| rs62245897 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453509 | AGGGTGGAGAAGTAG[G/T]CGGGAGGAAGCTATT | 10533 |
| rs62245898 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461882 | ATACAAAAAAAAAAT[A/T]AGCTGGGCGTGGTGG | 10533 |
| rs62245899 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465115 | TGTGTGTGTGTGTGT[A/T]AGGACACCTCCAGAG | 10533 |
| rs62245900 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465117 | TGTGTGTGTGTGTAA[A/G]GACACCTCCAGAGAG | 10533 |
| rs62245901 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466586 | GGCCTAGACTACAGC[A/G/T]TCGGTGCTTATAAGT | 10533 |
| rs62245902 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ATG7 | GRCh38.p7 | 3:11466999 | TGTGGTGGCGGGCGC[C/T]TGTAATCTCAGCTGC | 10533 |
| rs62245919 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475047 | TTTTTTTTTTTTTAA[A/T]TCCTGGCCACTGTGT | 10533 |
| rs62245920 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11477800 | CAGCCTAGACGCATT[C/T]TCTGTCCATGTCTCA | 10533 |
| rs62245922 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488367 | CCGGGCGGCACTCGC[C/T]GGCGCGGCGGCAAAG | 10533 |
| rs62245925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493881 | TGCCTAGAGGACTGA[C/T]TTCACTGCAGATTAC | 10533 |
| rs62245927 | snp | C/G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11501550 | ATAATGATATTAATA[C/G/T]ATAGGTGTGATAATG | 10533 |
| rs62245929 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11517360 | AAAAAAAGAAAAGAA[A/G]AGAAAAGAAAAAAAC | 10533 |
| rs62245930 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519190 | CAATTTTTTTTTAAC[C/T]AGCAAAAGGAATAAA | 10533 |
| rs62245948 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531866 | TGAGACCCTGTCTCA[A/G]GAAAAAAAAAAAAAA | 10533 |
| rs62245949 | snp | C/G | 0.328382 | 0.237395 | intron-variant | ATG7 | GRCh38.p7 | 3:11534495 | ATGGAGGAGAGGACA[C/G]CTCCCCAGAGCCAAG | 10533 |
| rs62245950 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ATG7 | GRCh38.p7 | 3:11534573 | CCGGGTGGCTACGTG[C/T]CGCCAGGCAGGGACT | 10533 |
| rs62245951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542738 | TCCTCCCGGGCACCC[C/G]CTCCCGGGCGTCAGG | 10533 |
| rs62245952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11545399 | ACAACAGATCCTTCT[A/C]TTGTGGGCATCGAGA | 10533 |
| rs62245954 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11547963 | CCTCCCACCTCAGCC[C/T]CCAGAGTAGCTGGGA | 10533 |
| rs62248255 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286804 | AGACGGAATGTTGCC[A/C]ATGTTGCCCAGGCTG | 10533 |
| rs62248256 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304859 | ATGTTGAGATATAAT[A/T]CATATACCATAAAAT | 10533 |
| rs62248257 | snp | C/G | 0.38286 | 0.211774 | intron-variant | ATG7 | GRCh38.p7 | 3:11308483 | GCTCTTTACTCTCCC[C/G]GTTCCCCAGCAGAGT | 10533 |
| rs62861960 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11390685 | TGATTTTTTTTTTTT[C/T]CCAGAAAGTAATTTG | 10533 |
| rs63554663 | snp | A/C/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11395969 | AAAAAAAAAAAAGGT[A/C/G]GGGGGGGAAGAGTAA | 10533 |
| rs66488222 | snp | C/T | 0.284209 | 0.247648 | intron-variant | ATG7 | GRCh38.p7 | 3:11534815 | TGGGACTGCACAGCA[C/T]CCCTTCTACCCTAGG | 10533 |
| rs66794993 | in-del | -/A | 0.472989 | 0.113031 | intron-variant | ATG7 | GRCh38.p7 | 3:11533540 | AATCCCCCTTCTGTT[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs66816143 | multinucleotide-polymorphism | GAG/TAT | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11337488 | TTATATATATATATA[GAG/TAT]AGAGAGAGAGAGAGA | 10533 |
| rs66962935 | in-del | -/AATG | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11553405 | ATGGGAGAGTGAAAG[-/AATG]GATGGATTGTGCTGG | 10533 |
| rs66974661 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | ATG7 | GRCh38.p7 | 3:11441255 | ATTTTTTATTTATTA[A/G]TTTTTTGAGATGGAG | 10533 |
| rs67030838 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486840 | TTTTTTTTTTTTTTT[-/T]AATTTATTTTTTTAT | 10533 |
| rs67085849 | in-del | -/CTATC | 0.202035 | 0.245356 | intron-variant | ATG7 | GRCh38.p7 | 3:11499258 | CATTGCCACATTCCT[-/CTATC]CTTTCCTGTTCTACA | 10533 |
| rs67095335 | in-del | -/AA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533555 | AAAAAAAAAAAAAAA[-/AA]AGCCATTACACAAAT | 10533 |
| rs67138683 | in-del | -/TTTTTTTTTT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11470004 | CCATCTCTCTCTCTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 10533 |
| rs67200586 | in-del | -/ACAC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502038 | ATATATACACACATA[-/ACAC]CACACATATGTTTAT | 10533 |
| rs67206280 | in-del | -/T/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439069 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTCAC | 10533 |
| rs67218196 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539102 | TCAACTGAGATTTTT[-/T]TTTTTTCAGGTTGTA | 10533 |
| rs67275894 | in-del | -/G | 0.316726 | 0.240931 | intron-variant | ATG7 | GRCh38.p7 | 3:11349240 | TGAGTGGGGACTTGG[-/G]AGAACTTTTCTGTCT | 10533 |
| rs67321508 | in-del | -/TTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314415 | TGATTAAATTTTTTT[-/TTG]TGTTGTTGTTCGTAC | 10533 |
| rs67338236 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495680 | TGTCTTTAAAACTCC[-/T]TGAAGCTGTAAGTCA | 10533 |
| rs67406430 | in-del | A/GG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468315 | CTGTGCTCTCCCACT[A/GG]GCTCCACTTACCCCT | 10533 |
| rs67470054 | in-del | -/GTGT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372802 | GTAGGTAAGGGCTGG[-/GTGT]GTGTGTGTGTGCGCG | 10533 |
| rs67487817 | in-del | -/G | 0.394171 | 0.204242 | intron-variant | ATG7 | GRCh38.p7 | 3:11319381 | TAGGAGGAGGAGGGG[-/G]CAGAATCAAGTAAAA | 10533 |
| rs67614461 | in-del | -/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515312 | GTGTGTGTGTATGTA[-/TG]TGTATTTTTGAGACA | 10533 |
| rs67745353 | snp | A/G | 0.29432 | 0.24604 | intron-variant | ATG7 | GRCh38.p7 | 3:11441360 | AAATTCTCTACCTCA[A/G]CCTCCCGAATAGCTG | 10533 |
| rs67754626 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391962 | TTGTACTTATTGGGG[-/G]GGGGGGTAATTTCAC | 10533 |
| rs67825010 | snp | C/T | 0.317933 | 0.240593 | intron-variant | ATG7 | GRCh38.p7 | 3:11383727 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGCATC | 10533 |
| rs67868453 | multinucleotide-polymorphism | GG/TA | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11395965 | AAAAAAAAAAAAAAG[GG/TA]GGGGGGGAAGAGTAA | 10533 |
| rs67890487 | in-del | -/AGT/GAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11463624 | AATTATCATAGGTGG[-/AGT/GAG]AGAGTGTTGGAGCAT | 10533 |
| rs67917615 | in-del | -/AAAGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396800 | AAAAAAAAAAAAGAA[-/AAAGA]AAGAAAAGAAAAGTA | 10533 |
| rs67974339 | in-del | -/CTC | 0.0879971 | 0.190408 | intron-variant | ATG7 | GRCh38.p7 | 3:11336896 | CAGGCTGGTCTTGAA[-/CTC]CTGGGCTCAAGCAAT | 10533 |
| rs68039111 | in-del | -/AAC | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11314425 | CCTCGGATTTGTACG[-/AAC]AACAACAACAAAAAA | 10533 |
| rs71044224 | in-del | -/TATATA | 0 | 0 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527088 | ATATGTATATGTATG[-/TATATA]TATATATATATATAT | 10533 |
| rs71055863 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11334970 | ATATCTCAGAAGAGA[-/TTTTTTT]TTTTTTTTTTTTTTT | 10533 |
| rs71055864 | in-del | -/TTTTC | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11339324 | CTAATTATACGCTGG[-/TTTTC]TTTTCTTTTCTTTTT | 10533 |
| rs71055868 | in-del | -/TTTTTTTTTTT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11411638 | CATATCTGATAAGAA[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 10533 |
| rs71055869 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11412262 | AAAAAAAAAAAAAAA[-/A]GAATCAAATAACTGG | 10533 |
| rs71055870 | in-del | -/AA | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11417829 | GCAAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAT | 10533 |
| rs71055875 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451608 | CAGCCACACTCACCC[-/T]TCACATTAGCTGGCA | 10533 |
| rs71055876 | in-del | -/CCCCCCAA | 0.479663 | 0.0987666 | intron-variant | ATG7 | GRCh38.p7 | 3:11452014 | CCCACAACCCCCCAA[-/CCCCCCAA]GTCCCTGGTGACCAT | 10533 |
| rs71055879 | in-del | -/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11463073 | ACATGGCAAAACCCC[-/C]ATCTCTACTAAAAAT | 10533 |
| rs71055880 | in-del | -/AC | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11465108 | GGTGTCCTTACACAC[-/AC]ACACACACACACACA | 10533 |
| rs71055881 | in-del | -/AAA/AAGAA/TAAA/TAAAAA | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11471761 | TAGAGACTACATTTC[-/AAA/AAGAA/TAAA/TAAAAA]AAAAAAAAAAAAAAA | 10533 |
| rs71055883 | in-del | -/A | 0.0825414 | 0.185628 | intron-variant | ATG7 | GRCh38.p7 | 3:11486821 | AAAAAAAAAAAAAAA[-/A]CAGAACCAAAGACAA | 10533 |
| rs71268441 | in-del | -/A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465459 | AAAAAAAAAAAAAAA[-/A/T]TGAGCCTGTAAGTCT | 10533 |
| rs71316461 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11274258 | ACTGCGCTGCAAGCT[A/G]GGAATACAAAAATGA | 10533 |
| rs71316462 | snp | A/G | 0.391583 | 0.206044 | intron-variant | ATG7 | GRCh38.p7 | 3:11277857 | CCTTATCTCAACTGC[A/G]TAAGACAGACACTCC | 10533 |
| rs71316464 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298665 | TGTTATTTTGCTGTG[G/T]TCTGTTTTGTTTTTT | 10533 |
| rs71316465 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303441 | TTGGGAGGCCGAGGC[A/G]GGTGGGTCACGAGGT | 10533 |
| rs71316466 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303444 | GGAGGCCGAGGCGGG[C/T]GGGTCACGAGGTCAG | 10533 |
| rs71316467 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303447 | GGCCGAGGCGGGTGG[A/G]TCACGAGGTCAGGAG | 10533 |
| rs71316468 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303466 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 10533 |
| rs71316469 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303479 | TCAAGACCATCCTGG[C/T]TAACATGGTGAAACC | 10533 |
| rs71316470 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303485 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 10533 |
| rs71316471 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304004 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCTGGGA | 10533 |
| rs71316472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304007 | GAGGCAGGAGAAAGG[C/T]GTGAACCTGGGAGGC | 10533 |
| rs71316473 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304015 | AGAAAGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 10533 |
| rs71316474 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304091 | GTGAGACTCCGTCTC[A/T]AAAAGAAAAAAATGT | 10533 |
| rs71316475 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304096 | ACTCCGTCTCAAAAA[A/G]AAAAAAATGTTTTTC | 10533 |
| rs71316477 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11395937 | AGAGCGAGACTCTGT[C/T]TCAAAAAAAAAAAAA | 10533 |
| rs71316478 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ATG7 | GRCh38.p7 | 3:11401469 | TAAAGTGAGATTCGT[A/G]TATAACAGCAGACAC | 10533 |
| rs71316481 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11415662 | CACTGCCTTCCACCT[C/T]TACATCGTGACCCAC | 10533 |
| rs71316482 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11421383 | TTCTAAATCTTTAGT[G/T]GTCATTTCAACAATG | 10533 |
| rs71316483 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11467606 | GTCTTGAACTCCTGA[C/T]CTCAGGTAATCCACC | 10533 |
| rs71316489 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11534955 | TCCTGGCAGAAGCCT[C/T]CACTCCAGCTGCAAT | 10533 |
| rs71316490 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11536807 | AGGCCACACCCCTCT[C/T]TGAGCCTCCATCTTC | 10533 |
| rs71316491 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11539891 | CACCTGCATCATTGC[A/G]TGTGTCAGCGCTTGG | 10533 |
| rs71316492 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11551173 | CGTCGTGTCCTGCGG[C/G]CCGTCTGAGTGTTCC | 10533 |
| rs71316493 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11553777 | TGGGTCCTCAGGAGA[A/G]AGGAAATTTCCTTCT | 10533 |
| rs71613897 | multinucleotide-polymorphism | AA/GT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11330198 | TTTCTCCACTGTAAA[AA/GT]TACTATTTTTTCTTT | 10533 |
| rs71613898 | multinucleotide-polymorphism | CG/TA | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11433017 | TGCATTTGGGATGGG[CG/TA]CAGTGGCTTACACCT | 10533 |
| rs71613899 | multinucleotide-polymorphism | AG/GA | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11497273 | TTCCCAGTGCTTGGG[AG/GA]GCCAAAGGTGGGTGG | 10533 |
| rs71624908 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11451804 | AAAAAAAAAAACAAA[A/T]TAAAAAAACCCCAGG | 10533 |
| rs71624909 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11488325 | TCGGGCCCCGCGGGG[C/T]CCGTCCGCTCCTCCA | 10533 |
| rs71624911 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11497270 | GTATTCCCAGTGCTT[G/T]GGAGGCCAAAGGTGG | 10533 |
| rs71626307 | multinucleotide-polymorphism | ACTCTGTCACCCAGGCTGGAGTGCAGTCGTG/GCTCTGTCGCCCAGGCCGGAGTGCAGTGGCA | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11304077 | TTGAGACGGAGTCTC[lengthTooLong]CGATCTCGGCTCACT | 10533 |
| rs71626308 | multinucleotide-polymorphism | CCGAGT/TCAAGC | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303980 | TCCTGCCTCAGCCTC[CCGAGT/TCAAGC]AGCTGGGACTACAGG | 10533 |
| rs71626309 | in-del | GTG/TTTTTTTTTTTTTTTTTGCA | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303935 | CCCGGCTAATTTTTT[GTG/TTTTTTTTTTTTTTTTTGCA]TTTTTAGTAGAGACG | 10533 |
| rs71626995 | in-del | -/CCCC | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11277891 | GCGGCCCTTTATAGA[-/CCCC]CCCCCCCCCCCCCAC | 10533 |
| rs71626996 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11280204 | CGCCTGCCACCCATG[-/G]CCCGGCCCTTTTTTT | 10533 |
| rs71626997 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11284864 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 10533 |
| rs71626998 | in-del | -/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11293707 | ACAAAACATTAGGGC[-/C]AGGCATGGTGGCTCA | 10533 |
| rs71626999 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11293710 | AACATTAGGGCCAGG[-/G]CATGGTGGCTCACGC | 10533 |
| rs71627001 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303960 | GCCGGGCGTGGTGGC[-/G]GGCGCCTGTAGTCCC | 10533 |
| rs71627002 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11325401 | ATAGGCCAGGCGTGG[-/G]TGGCTCACGCCTGTA | 10533 |
| rs71628703 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11334145 | TAAATGTTATGTAAA[-/T]TTTCCTAGCTCACAT | 10533 |
| rs71628705 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11359628 | TTGAGCCTGGGAGGT[-/T]GAGGCTGCAGTGAAC | 10533 |
| rs71628706 | in-del | -/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11374627 | AAAGCACAAAAAGTC[-/C]ATGTGTGGTGGCTCA | 10533 |
| rs71628707 | in-del | -/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11374655 | TCACGCCTGTAATCC[-/C]AGCACTTTGGGAGTC | 10533 |
| rs71628708 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11389456 | TTTTTTTTTTTTTTT[-/T]AACACAGAATAAGCT | 10533 |
| rs71628709 | in-del | -/ACAA | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11392473 | TAAAAAAACAAACAA[-/ACAA]AAAAAACAAAACAAA | 10533 |
| rs71628713 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11422814 | TGGAGTGCAGTGTGG[-/G]CGCAATCTCAGCTCA | 10533 |
| rs71628714 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11424387 | TTAAATAAAGGTGGG[-/G]AGGATCACCTGAACC | 10533 |
| rs71628716 | in-del | -/ACCAAGTGTGTAGTAA | 0.499908 | 0.00678851 | intron-variant | ATG7 | GRCh38.p7 | 3:11474077 | GTTCAGTTCAGACTT[-/ACCAAGTGTGTAGTAA]GCCAAGTGCCACCAC | 10533 |
| rs71628717 | in-del | -/CACA | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11479040 | ACACACACACACACA[-/CACA]ATTTTTTACTTTGTG | 10533 |
| rs71628719 | in-del | -/C | 0.5 | 0 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527398 | GCCACCACGCCTGGC[-/C]TTTTTTTCTTATATT | 10533 |
| rs71628720 | in-del | -/A | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11538728 | AAAAAAAAAAAAAAA[-/A]GCCAGATGTGGTGGT | 10533 |
| rs71893669 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11403336 | TTTCTTTTTTTTTTT[-/TT]TAATCTCTTAAGGGT | 10533 |
| rs71915215 | in-del | -/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367004 | TGTGTGTGTGTGTGT[-/TG]GTGTGTGTGTTTACT | 10533 |
| rs71939569 | in-del | -/GT/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465090 | CTAAAGTGTGTGTGT[-/GT/TG]GTGTGTGTGTGTGTG | 10533 |
| rs72033868 | in-del | -/AAAAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396794 | TCCAAAAAAAAAAAA[-/AAAAG]AAAGAAAAGAAAAGA | 10533 |
| rs72147868 | in-del | -/GTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314423 | TTTTTTTTGTTGTTG[-/GTT]TTCGTACAAATCCGA | 10533 |
| rs72177700 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440699 | TTTTTTTTTTTTTTT[-/TT]TGAGACGGACTTTCG | 10533 |
| rs72228304 | in-del | -/AAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470005 | AAAAAAAAAAAAAAA[-/AAAAA]AAAAGAGAGAGAGAG | 10533 |
| rs72319730 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351852 | TCTTTTTTTTTTTTT[-/T]ATTATACTTTAAGTT | 10533 |
| rs72396055 | in-del | -/TTTCTTTCTTTCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295760 | GTTTTACTGGTTCTA[-/TTTCTTTCTTTCT]TTTCTTTCTTTCTTT | 10533 |
| rs72507378 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395968 | AAAAAAAAAAAAAGG[-/TA]GGGGGGGAAGAGTAA | 10533 |
| rs72580740 | in-del | -/C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495678 | GCTGTCTTTAAAACT[-/C/T]CCTGAAGCTGTAAGT | 10533 |
| rs72580742 | in-del | -/A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11507961 | GTAATTAAAAAAAAA[-/A/C]AMMAAAAAACAAAAA | 10533 |
| rs72624430 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474077 | GTTCAGTTCAGACTT[A/G]CCAAGTGTGTAGTAA | 10533 |
| rs73011786 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270408 | AAAATGCTTATTAAC[C/T]AAACTTGGGTTAAGC | 10533 |
| rs73011792 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | ATG7 | GRCh38.p7 | 3:11277310 | CATAAGGCTCTTCAT[G/T]ATATGGCCTTTGCCT | 10533 |
| rs73015741 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ATG7 | GRCh38.p7 | 3:11312173 | GTGAATTTTATGGAA[C/T]GTAAATTATATCTCA | 10533 |
| rs73015744 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11314414 | ATTGATTAAATTTTT[G/T]TTGTTGTTGTTCGTA | 10533 |
| rs73015760 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11323777 | CACTTAGTGATCTCT[C/T]CGCATCTTGGCAGCT | 10533 |
| rs73017651 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ATG7 | GRCh38.p7 | 3:11396119 | AATCAGAAGTATAGG[A/G]AAAAAAAAAAAGTAT | 10533 |
| rs73017659 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ATG7 | GRCh38.p7 | 3:11397158 | GATTTTTAAATTTAT[A/G]TGCATTATACAAGCA | 10533 |
| rs73017678 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11412219 | AGAGAGGGGTAAGGA[A/G]GCATCTGGTGCTGTG | 10533 |
| rs73017684 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11418914 | GTGCCACTTTTAAAT[A/C]ATCAGATCTCATGAG | 10533 |
| rs73017695 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11425118 | CAGGTGCACTCCACC[A/G]TGCCTGGCTAATTTT | 10533 |
| rs73019529 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11442740 | AGACTCCATCTCTAC[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs73019544 | snp | C/T | 0.331411 | 0.236373 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451303 | TGAAACCTCGGCCTC[C/T]TGGGTACAAGTGATT | 10533 |
| rs73019547 | snp | A/C | 0.498589 | 0.02652 | intron-variant | ATG7 | GRCh38.p7 | 3:11451849 | TCTATCTCTCTCTCT[A/C]TATATATATACGCCT | 10533 |
| rs73019556 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | ATG7 | GRCh38.p7 | 3:11455889 | CTAACCTGTCTTATG[C/T]TCTTTCAAACCATCT | 10533 |
| rs73019559 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11456195 | ATCTTTCGTCTCTTC[A/G]GATTTGCGTGTTCTG | 10533 |
| rs73019581 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | ATG7 | GRCh38.p7 | 3:11469664 | CCTGTCCACTGCAGC[C/G]CAGCTAATGTCTTAC | 10533 |
| rs73019595 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11475425 | CATGATGGGCAGGGG[C/G]CTGGCGAGATGCGTC | 10533 |
| rs73021306 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11483201 | CCCCCTGCCCCTAAC[C/T]CAGGTCATGGAGAGG | 10533 |
| rs73021317 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11495099 | AAAAAAGGCTTGAAC[A/G]GATGTTCTCTAAGGC | 10533 |
| rs73021332 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11520651 | AGCACACACATTCTA[C/T]ACTTCTGAGCTCGCC | 10533 |
| rs73021344 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11531883 | AAAAAAAAAAAAAAA[A/G]AAAAAGTCTAATAAC | 10533 |
| rs73021345 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | ATG7 | GRCh38.p7 | 3:11534638 | GAGCTGCCACACGCC[A/G]TCTGTTAGCAGGACA | 10533 |
| rs73021346 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11534891 | GCGCTTCAGGCCCAC[A/G]TAGGCGCAGCCCTGC | 10533 |
| rs73122106 | snp | C/T | 0.197082 | 0.244335 | intron-variant | ATG7 | GRCh38.p7 | 3:11408465 | CTTCCACATTTTGGG[C/T]ATCTTTTCAGCAACA | 10533 |
| rs73122114 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ATG7 | GRCh38.p7 | 3:11415147 | CAACTATAACACAAC[A/G]GTAAGTACTTGTGTA | 10533 |
| rs73122118 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ATG7 | GRCh38.p7 | 3:11422411 | TTCCTTAAACCTCAT[C/T]AGCCAACCTCTGCTA | 10533 |
| rs73122122 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ATG7 | GRCh38.p7 | 3:11424575 | GTATTTATTATCGGT[A/G]GCAATTAAATAATTT | 10533 |
| rs73123007 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11522101 | AGTGACCAAGCCAGG[A/G]TTCCGTTTCAGATCT | 10533 |
| rs73123008 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11523047 | TAGCCTGTACTTTAT[A/G]AAGTATGTTGTAAAT | 10533 |
| rs73123011 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ATG7 | GRCh38.p7 | 3:11523384 | ATACGGGGTACATCT[A/G]TCTGGCCTGTCTCTA | 10533 |
| rs73123022 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | ATG7 | GRCh38.p7 | 3:11529219 | GGTTGAAGAGTTGGG[A/C]GTTTGCTTTGTTTTT | 10533 |
| rs73123024 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | ATG7 | GRCh38.p7 | 3:11529602 | GATGTTATCAGCAAC[A/G]TGAAGTTTGTCCCTG | 10533 |
| rs73123026 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11530663 | ATCTTTCTCTCTTCA[A/G]TCCTTCTTAATAATA | 10533 |
| rs73123036 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11533615 | CTTCTCTGAAATGAC[A/G]AAAAACTCATTAAAA | 10533 |
| rs73123047 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11537596 | GGGGTCACAATGAGA[A/G]TGATTATAAAACAAA | 10533 |
| rs73123055 | snp | C/T | 0.079617 | 0.182947 | intron-variant | ATG7 | GRCh38.p7 | 3:11540196 | TGGTTGTGCCATGTG[C/T]TTGTCAGCACTTGGA | 10533 |
| rs73123330 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11275986 | AGACTGCACTTTTCT[C/T]GTGGTAACCTAAAGC | 10533 |
| rs73123390 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11277406 | TCAGGGGAACCTGCC[C/T]CCAATATTTCAAGGT | 10533 |
| rs73123398 | snp | A/T | 0.126909 | 0.217598 | intron-variant | ATG7 | GRCh38.p7 | 3:11290376 | AGGCCAGGCCAAGCA[A/T]GAGGAATAAGCTGTC | 10533 |
| rs73123400 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11290926 | CTTACCAAGTGATCC[A/C]CCCACCTCAGCCTCC | 10533 |
| rs73123401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300207 | GCTGCTGGGATTACA[C/T]GATCGAGCCACCACA | 10533 |
| rs73123402 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11301463 | ATTTTTTTTAATCTC[A/G]GAAAATCAATACTTT | 10533 |
| rs73125406 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ATG7 | GRCh38.p7 | 3:11303379 | AGCTGAGAAAAAAAA[A/G]GAATTTTCCGCCAGG | 10533 |
| rs73125409 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ATG7 | GRCh38.p7 | 3:11304839 | TTGAATTCTTTTTAG[C/G]AGCTATGTTGAGATA | 10533 |
| rs73125411 | snp | C/T | 0.102014 | 0.201495 | intron-variant | ATG7 | GRCh38.p7 | 3:11305361 | GCAGTTTTCTCCTTT[C/T]ACAAAATGAGGCTTT | 10533 |
| rs73125415 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ATG7 | GRCh38.p7 | 3:11313075 | TCAATAAAGTATATT[A/G]TGTTTGTCATCATAT | 10533 |
| rs73125418 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | ATG7 | GRCh38.p7 | 3:11313717 | AGGTGATCCTCTCAT[C/T]TCAGCCTCCTGAGCA | 10533 |
| rs73125426 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ATG7 | GRCh38.p7 | 3:11318125 | AATCTCTGGGGTCTC[C/T]TCTGAAGTGCTCTGA | 10533 |
| rs73125430 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | ATG7 | GRCh38.p7 | 3:11320192 | ACCTCCCCTTTGCTC[C/T]GTTAAGTGCTCACTC | 10533 |
| rs73125433 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11320234 | CCTTCCCTGACCTCT[A/G]TAAAAAGGTTTATTC | 10533 |
| rs73125438 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11323098 | AATGAAACTGTCAAA[A/G]AAAAAAGTTAGAACA | 10533 |
| rs73125442 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ATG7 | GRCh38.p7 | 3:11327424 | CATAAGAATCACATG[C/T]GGTATTCACTGGACA | 10533 |
| rs73127221 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11334827 | GCTACGTGTGGTGGC[A/G]GGCGTCTGTAATCCC | 10533 |
| rs73127225 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11339816 | GCCAAATCAAATCAC[A/G]TGGGTTCTGTACTGC | 10533 |
| rs73127229 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ATG7 | GRCh38.p7 | 3:11346207 | GTAGAATATGCCTTC[C/T]GATAGGATGAAACAT | 10533 |
| rs73127234 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356448 | CTGATATACAGCCAA[A/C/G]TAGAAAACCACTGTG | 10533 |
| rs73127242 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | ATG7 | GRCh38.p7 | 3:11365804 | CCACAATCCATACCT[A/C]AACTTGGCAGTCTGA | 10533 |
| rs73127245 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11369632 | CAAGGAAGGATCCGG[A/G]TATAGGTCTAACAAT | 10533 |
| rs73127248 | snp | A/C/G | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11373705 | GCCTGGCCTCTCTCA[A/C/G]TAGGTATGTGTATAT | 10533 |
| rs73127250 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11374350 | GAATGCCGTTTTCAA[C/G]AAATAGTATGGAGAC | 10533 |
| rs73127256 | snp | A/C | 0.140581 | 0.224783 | intron-variant | ATG7 | GRCh38.p7 | 3:11385832 | GTTATGAAGTTGTTT[A/C]GTAGAGCAGTTGTGG | 10533 |
| rs73127259 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11386787 | GTGTGGTATAAAATA[C/T]ATCCCACATCTTGTC | 10533 |
| rs73137555 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | ATG7 | GRCh38.p7 | 3:11438064 | TGATATCCACTTAAG[C/T]ATATCTTTTTAATTC | 10533 |
| rs73137563 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11439846 | ACTAATGTTAATTGC[A/G]TTATCTGTGATTTTC | 10533 |
| rs73137567 | snp | A/G | 0.078151 | 0.181571 | intron-variant | ATG7 | GRCh38.p7 | 3:11444078 | AAACAGAATTATGCT[A/G]TAATATGTAGATTCT | 10533 |
| rs73137574 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11448982 | TAGGGTAAAAATGTC[A/C]CACAAAGTCTGTATT | 10533 |
| rs73137583 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11452790 | TTTTCTTGATAGGAG[A/G]TAATTATTGCAGATA | 10533 |
| rs73137585 | snp | A/G | 0.190519 | 0.242821 | intron-variant | ATG7 | GRCh38.p7 | 3:11453424 | TTATTTCCCGCCGTG[A/G]CTGTCCCTGCAAGCC | 10533 |
| rs73138950 | snp | C/T | 0.199564 | 0.24486 | intron-variant | ATG7 | GRCh38.p7 | 3:11389500 | CTCTAGAATATCTAA[C/T]GACTGGTTAAATCAC | 10533 |
| rs73138952 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | ATG7 | GRCh38.p7 | 3:11391849 | AGGCTCAGAGAAATT[A/C]CATGAAAGTCCAGGA | 10533 |
| rs73138953 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11392970 | CCTGTGGACTGGGAA[A/G]AGCCCCAACCTGTCC | 10533 |
| rs73138968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400872 | TAGTGAAACCTGGCT[C/T]TCTCTGCAGGGGAAT | 10533 |
| rs73139503 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ATG7 | GRCh38.p7 | 3:11463413 | AAACCTTCAGTCTTG[C/T]TGAACCAATTGGTTC | 10533 |
| rs73139508 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ATG7 | GRCh38.p7 | 3:11466747 | ACTCAACTGTTGGAT[A/G]CATTAGCATCAGAAT | 10533 |
| rs73139516 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11474996 | ACCTAGCTTATGTTG[C/T]GTTTGAAGCAGGAGA | 10533 |
| rs73139518 | snp | G/T | 0.190519 | 0.242821 | intron-variant | ATG7 | GRCh38.p7 | 3:11477460 | TTTCTCCCTCTAATT[G/T]ATAAATGTCAGCACT | 10533 |
| rs73139526 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | ATG7 | GRCh38.p7 | 3:11480479 | TATTGGGAGGGGGTG[C/T]GATGGTTTGCGGCAG | 10533 |
| rs73139531 | snp | C/T | 0.0659991 | 0.169416 | intron-variant | ATG7 | GRCh38.p7 | 3:11483137 | GTAAATTTAGAAATC[C/T]CTTTTCTGCTCTCCT | 10533 |
| rs73139548 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11499463 | TGAAAATCTAAAATA[C/T]GGCCAGGCGCAGTGG | 10533 |
| rs73139551 | snp | A/G | 0.190205 | 0.242744 | intron-variant | ATG7 | GRCh38.p7 | 3:11503171 | TCGGGGGCTCTTTGA[A/G]TGACAGTCGGCCAGA | 10533 |
| rs73139562 | snp | C/T | 0.0322114 | 0.122752 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510767 | TGGCAGTCAGACTTC[C/T]AGGCTTGGGGTAGAA | 10533 |
| rs73812419 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271687 | TATAACTTGGGGATA[C/T]GTTTCAGGACTCTTG | 10533 |
| rs73812420 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11274106 | TCCTTCCTGCCCTCA[C/T]GTGACATGATTTTGA | 10533 |
| rs73812421 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11275666 | TCCTCTCCCCTTTCT[A/G]TCTCCTGATCTCCCC | 10533 |
| rs73812422 | snp | C/G | 0.0656901 | 0.169351 | intron-variant | ATG7 | GRCh38.p7 | 3:11279768 | TTTCTATAGGAAACA[C/G]TGTTGCCTCATCAGT | 10533 |
| rs73812424 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11283497 | GTGCAGGGGGGTGAA[A/G]GAACCTGCCCTAACC | 10533 |
| rs73812426 | snp | C/T | 0.00224001 | 0.0333914 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298694 | TTAATAGGCAAGAAA[C/T]AATGGCGGCAGCTAC | 10533 |
| rs73812428 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11311852 | TGAATAGCAGAATTA[C/G]AGACCGCAGAGATTA | 10533 |
| rs73812429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11318213 | GCACACTATCCTTCA[C/T]TTGGTTAGGGTGGTA | 10533 |
| rs73812430 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | ATG7 | GRCh38.p7 | 3:11319241 | CATTAACCTTGTTCA[A/C]TCTCTTTAGCATGAT | 10533 |
| rs73812436 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11346525 | TCTTTAATCTTTGCA[G/T]ATTAGCCATTTAAAC | 10533 |
| rs73812437 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11346618 | TATGGCATGTTTGTA[A/C]TGTATCTGGCTTTCT | 10533 |
| rs73812438 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11346662 | CACGTTCCCAGAGTG[C/G]CTTCCTTGCTATCCA | 10533 |
| rs73812442 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11361998 | ATGCCCTCCCAATAT[A/G]AAGAAAAGAAGATGA | 10533 |
| rs73812443 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11384216 | GCAGGAGGAGACTGC[A/G]TGCAGAGTATTCTTG | 10533 |
| rs73812444 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11389925 | CATATTTTTGTGTTA[C/T]GTGCGAAGGCCTGGG | 10533 |
| rs73812445 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11392797 | TTGTGGCTCCTAATG[A/G]TGCAAGTTTTTTGTT | 10533 |
| rs73812446 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ATG7 | GRCh38.p7 | 3:11400510 | ACTACTGGGAATAAC[A/G]TTGCCATATTTTCTG | 10533 |
| rs73812449 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11409227 | TTTCAATTTACCATG[A/G]TGTGAGAGTAATAGG | 10533 |
| rs73812458 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11454401 | GAAACTTTGGCTAAG[A/G]GGCTGCGATTAGAAT | 10533 |
| rs73812461 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11459961 | TGGGGTCTGTGCTCT[C/T]ATCCACTGCACCATA | 10533 |
| rs73812462 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11464606 | ACCTGGGAATGCCAG[A/G]TGGACTTGTTGTTTT | 10533 |
| rs73812463 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11483536 | GTGCGAATGTCAAGC[A/G]TGTTGAATTGTCAGT | 10533 |
| rs73812464 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11492513 | TATTTTCTTGACACC[C/G]TTTGCTGAGGGACTC | 10533 |
| rs73812469 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11555008 | TGGCCAGTGTTCGGC[A/G]TTGCTCGGGATTCAA | 10533 |
| rs73812470 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556830 | TAGGGGCCTGAATGC[C/T]AAAGCTTGGAAGCCC | 10533 |
| rs74279976 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11372851 | GCGTGCGTGCGTGTG[C/T]GTGTGTGTGTGTGAA | 10533 |
| rs74339933 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465644 | TGGCACACACCTGTA[-/A]GTCCTAGCTACTTGG | 10533 |
| rs74418186 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11539819 | GAACCAGCACAGTTC[A/G]GCGACATCGAGCAGG | 10533 |
| rs74422234 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11289893 | AAAAGTAGTTTATTT[A/G]TTCTGTTTACAAAGT | 10533 |
| rs74422548 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11324478 | CCTGCCTTCTGCACT[C/T]ATGCCTCATATGGGT | 10533 |
| rs74453050 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11504148 | GAACAAAAGACAGTC[A/G]AGAGGGGGAAAAAAG | 10533 |
| rs74470410 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372847 | GTGTGCGTGCGTGCG[C/T]GTGCGTGTGTGTGTG | 10533 |
| rs74488174 | snp | A/G | 0.328148 | 0.237472 | intron-variant | ATG7 | GRCh38.p7 | 3:11485861 | agttgtagatatgcg[A/G]cgttatttctgaggg | 10533 |
| rs74528647 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | ATG7 | GRCh38.p7 | 3:11535175 | TCGGGGCCTGGACCC[A/G]GGCCATGCCCTGCTG | 10533 |
| rs74535069 | snp | G/T | 0.124491 | 0.216211 | intron-variant | ATG7 | GRCh38.p7 | 3:11530474 | GCTGAATTGGGAAAT[G/T]ATGATTTGCTTTAAA | 10533 |
| rs74537877 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11534598 | GGGACTGCATACTGC[A/G]GTTTCGTAGTCGCTG | 10533 |
| rs74571089 | in-del | -/GCCAGGGAAAGGTGGAGGGAAGAGGGCATAGGTCCCAGTGTGG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537997 | CTGAATGTAGAAGAG[lengthTooLong]GATTCCAGATGACCC | 10533 |
| rs74606893 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11548186 | CTTTTTATTATTGCG[C/T]TGTAAATGGCCTTTG | 10533 |
| rs74624034 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531794 | ACCTGAGCCCAGGAG[G/T]TTGAGGCTGCAGTGA | 10533 |
| rs74627610 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11495962 | TCATTTTCATAGGCG[C/T]GTCACGCTAGCATTT | 10533 |
| rs74631751 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11420310 | TAATAATGTTCCAGC[A/G]TTAAACTTTCTGTAC | 10533 |
| rs74696458 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531740 | ATGATGGCACATGTC[C/T]GTAGTCCCAGCTACT | 10533 |
| rs74712401 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11323094 | ACAGAATGAAACTGT[A/C]AAAAAAAAAAGTTAG | 10533 |
| rs74719560 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11508240 | CACAGTGTCTAAGGT[A/G/T]GGGGGGTGTCCAATC | 10533 |
| rs74809623 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11399856 | TGGGATTACACGTGA[G/T]CCACAGTGCCTGGCG | 10533 |
| rs74820724 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | ATG7 | GRCh38.p7 | 3:11522781 | TGCCCACCCCAGGCC[G/T]AGACTGCTCTGAGCT | 10533 |
| rs74843503 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11409048 | GTATTTTGGATAATA[A/G]TCCTTTATTAAATGT | 10533 |
| rs74849862 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11546836 | CGGCCAGTGGGGAGC[G/T]CTGAGGTGCTCAGGT | 10533 |
| rs74883573 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11481154 | AGCACTGTGTAAGCA[A/C]CTACTGTTGAGAACA | 10533 |
| rs74891883 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11377151 | CTAGAAGGGAGGGAG[C/T]CCACCTGTGGAAGTA | 10533 |
| rs74899971 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11428295 | CTGGACCAGCCAGTG[C/G]TGAAAGGGCTGCTGT | 10533 |
| rs74902175 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487665 | CACCTCCCTCCCGGA[C/T]GGCACGGCTGGCCAG | 10533 |
| rs74910111 | in-del | -/GTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501548 | GATAATGATATTAAT[-/GTTA]AGATAGGTGTGATAA | 10533 |
| rs74917053 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11522382 | TCCTTTCTGCTAACT[A/G]TAGGTGGGTTTACAG | 10533 |
| rs74924891 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11326974 | GGAACTTGCTGAGAT[A/G]CTGCATCACAGTTTT | 10533 |
| rs74929740 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11380521 | AGGGCCCCTTCAGCT[C/T]TGATCTTTCCAGAAG | 10533 |
| rs74933978 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11423631 | TGCCTTTTTTTTTTC[C/T]AGGGGGTTAGGCTGT | 10533 |
| rs74938850 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11372813 | CTGGGTGTGTGTGTG[C/T]GTGCGCGCGTGTGCG | 10533 |
| rs74943470 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11328070 | ATTCAAGTCCATGGA[A/G]TGGACCAGCTGCATC | 10533 |
| rs75017044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514507 | GTTCCAGGAAATACC[A/G]CCCAGTCTTTTTACC | 10533 |
| rs75048647 | snp | C/T | 0.110872 | 0.20771 | intron-variant | ATG7 | GRCh38.p7 | 3:11416198 | TATCTGGCTTTGGTA[C/T]TAGGGTGATGCTGGC | 10533 |
| rs75068138 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452572 | CATAAAAAGGTCCTC[A/T]AGGCACTTCAGCAAA | 10533 |
| rs75075577 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11545349 | AGAGGCTTATGGACA[C/T]CCCAGAAGAACCACG | 10533 |
| rs75078925 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11407621 | ATTTCAGAGGATATA[C/T]GGAAACTCCTGGATG | 10533 |
| rs75148459 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11531793 | CACCTGAGCCCAGGA[A/G]GTTGAGGCTGCAGTG | 10533 |
| rs75167768 | snp | C/T | 0.0502586 | 0.150675 | intron-variant | ATG7 | GRCh38.p7 | 3:11539740 | TAAAATCTATTGATG[C/T]GCATACAATCAAATA | 10533 |
| rs75170019 | snp | C/T | 0.207559 | 0.246371 | intron-variant | ATG7 | GRCh38.p7 | 3:11398292 | TTTCAAGCACACACA[C/T]AATATTTTACAAGAA | 10533 |
| rs75185054 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484487 | AGCATTTTAATCCAT[A/C]ATTTAGGACAAAATT | 10533 |
| rs75205131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11456729 | GTTTGGACTCAAAAA[C/T]GTGACGGAAAGAAGT | 10533 |
| rs75222708 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474402 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGGCAACAT | 10533 |
| rs75228590 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ATG7 | GRCh38.p7 | 3:11528172 | AGATAACCATTTCAC[A/G]GGGCAAGGTTTTCTG | 10533 |
| rs75236077 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | ATG7 | GRCh38.p7 | 3:11442225 | GTGTGGGCCCAGAAA[C/G]AGGGTGGTCTTATGG | 10533 |
| rs75238550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349867 | GGTTTTTGAGTTATA[C/T]CATTAGAAATACCAG | 10533 |
| rs75285348 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531819 | CAGTGAGCCCAGATC[C/G]TACCACTGCACTTCA | 10533 |
| rs75298356 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487494 | CCCTCCCGGACAGGG[C/T]GGCTGGCCGGGCAGA | 10533 |
| rs75314662 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298570 | TGTTTCAAGGTAGCC[C/T]GTAAACATCTCATTA | 10533 |
| rs75326775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431024 | TCATGAGTAGTGTGA[G/T]GTACTTGGAGCCACA | 10533 |
| rs75353105 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11540958 | AGGCTGGAGTGCAGT[C/G]GTGCAATCTTGGCTC | 10533 |
| rs75390140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11364879 | GGAGAGCTTTCTGAC[C/T]ACCTGGAAGGTATTC | 10533 |
| rs75416366 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531814 | GGCTGCAGTGAGCCC[A/T]GATCCTACCACTGCA | 10533 |
| rs75438291 | snp | A/G | 0.111928 | 0.208413 | intron-variant | ATG7 | GRCh38.p7 | 3:11421759 | CCCTGTATGGCAGCT[A/G]TTGCCTTATTAAATG | 10533 |
| rs75470827 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11486853 | TTTAATTTATTTTTT[A/T]ATTGATAATTCTTGG | 10533 |
| rs75474760 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ATG7 | GRCh38.p7 | 3:11394530 | GGAAGTTGAGAGCGT[A/G]AGCCACACCTTTAGT | 10533 |
| rs75475604 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11502980 | AGAGTTGAAAGTAGC[A/G]TGTATACCACTGAAA | 10533 |
| rs75483053 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | ATG7 | GRCh38.p7 | 3:11309460 | TTGTTGATTTTTTTT[G/T]TTTGTTTTTTTAAAG | 10533 |
| rs75486088 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | ATG7 | GRCh38.p7 | 3:11552963 | CCCCGGCCCAGGCCC[G/T]AGTCCTCTTATGAAC | 10533 |
| rs75492008 | snp | C/T | 0.0543475 | 0.155628 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282230 | GGTATCCAGTGCATC[C/T]GTTCTCAAAAACTGA | 10533 |
| rs75500213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11420480 | ATCATGTCTGGGGCT[C/T]TTCCAATTTTTATTC | 10533 |
| rs75504006 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11539671 | ATATGTTTTTATATT[C/G]TGAAACTCCCCCCGT | 10533 |
| rs75518699 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11372558 | TTCCACAAATGAGAT[-/A]ACAGAATTTTTCTGT | 10533 |
| rs75529549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323781 | TAGTGATCTCTCCGC[A/G]TCTTGGCAGCTGTCT | 10533 |
| rs75553263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274663 | CTTTGGGATCCAAGA[C/T]AGCTGCGTACCAATA | 10533 |
| rs75554906 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | ATG7 | GRCh38.p7 | 3:11523630 | TTGCTCTGGGCCTGA[C/T]TTCCTTTGCACACTC | 10533 |
| rs75634077 | snp | A/G | 0.110519 | 0.207473 | intron-variant | ATG7 | GRCh38.p7 | 3:11421474 | AAGAAGCAACTCCTC[A/G]TCTGTTCAAGTTTGA | 10533 |
| rs75644524 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | ATG7 | GRCh38.p7 | 3:11296129 | CATTCTCTAGGACTT[G/T]GTGGGGCTTTTTCTT | 10533 |
| rs75646038 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ATG7 | GRCh38.p7 | 3:11482383 | CTTCCCTTGGCTTCT[A/T]CTGACCTCTTGTCCC | 10533 |
| rs75646199 | in-del | -/TTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501546 | TAGATAATGATATTA[-/TTG]ATAGATAGGTGTGAT | 10533 |
| rs75648188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11411153 | TTCTAATGTATGTGA[A/G]GTGGGGTCTCACTGT | 10533 |
| rs75660726 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | ATG7 | GRCh38.p7 | 3:11275241 | CTTTGACTAGTGTCT[C/T]TAATAGATTAACCCT | 10533 |
| rs75671842 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11386793 | TATAAAATATATCCC[A/G]CATCTTGTCCTTAGC | 10533 |
| rs75675057 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11463622 | TTGAATTATCATAGG[A/T]GGAGAGTGTTGGAGC | 10533 |
| rs75699968 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11449929 | CCTGGAGTTGAAGTA[A/C]ATTCAACAGCATCAA | 10533 |
| rs75730403 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ATG7 | GRCh38.p7 | 3:11417443 | TCTTTATCTAATAAC[A/G]TTATTTGCTTTGAAG | 10533 |
| rs75731276 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11372827 | GTGTGCGCGCGTGTG[C/T]GTGTGTGTGCGTGCG | 10533 |
| rs75737361 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11282942 | GTCATGTGGTTTGGT[G/T]CTTATTTTAATGACT | 10533 |
| rs75772706 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | ATG7 | GRCh38.p7 | 3:11403155 | TGAGATACAATTTAC[A/C]TACCAGAAAATCCAC | 10533 |
| rs75787979 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11316968 | TTTAAAATCAACTAC[A/G]TTTACATTTTATTTT | 10533 |
| rs75806401 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11390373 | GGAGCAAGAGTTTCA[G/T]TTAACAATATCTGCT | 10533 |
| rs75822807 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | ATG7 | GRCh38.p7 | 3:11315970 | ATGCGTGACCTGCTT[C/T]GGCCTCCCAAACTGC | 10533 |
| rs75825011 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11274189 | TTTTTCGTTCCCAGC[C/T]AGCATCTCATTATAG | 10533 |
| rs75835152 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309465 | GATTTTTTTTTTTTG[G/T]TTTTTTAAAGACAGA | 10533 |
| rs75864032 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ATG7 | GRCh38.p7 | 3:11548028 | TAAATTTTTTTGATA[A/G]AGACAGGATTTCCCT | 10533 |
| rs75883056 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288605 | AAAAGGTCATGCAGT[A/G]AAAATAAGTCTCCCC | 10533 |
| rs75885101 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | ATG7 | GRCh38.p7 | 3:11274694 | TTCCCATTGCCACTG[A/C]ACTAGTTTTGTGACC | 10533 |
| rs75889707 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ATG7 | GRCh38.p7 | 3:11553459 | TTTCTTCCACTCGGA[C/T]CATCAGAACCCAGAG | 10533 |
| rs75899726 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11429947 | CGAGACTCTGTCTCA[A/G]GAAAAAAAAAAAAAA | 10533 |
| rs75909114 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11311604 | AGCAAGACTGTCTCC[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs75929295 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11297220 | AAAATTAGCCAGTCA[C/T]GGTAGCCCATGCCTG | 10533 |
| rs75929731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330788 | TCTTCACTGAAGAAA[C/T]GGTATTTTAAATTGA | 10533 |
| rs75951568 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11328087 | GGACCAGCTGCATCA[C/G]AATTATTCAGGAGCC | 10533 |
| rs75953482 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273786 | TGGTGGTGGTGGCGG[G/T]GGCGGCATTGTCAGT | 10533 |
| rs75982152 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11460985 | GAATATATACAGTAC[C/T]ACCAGTAGTAAGTCA | 10533 |
| rs75983351 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487679 | ATGGCACGGCTGGCC[A/G]GGCGGGGGGCTGACC | 10533 |
| rs75989564 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11472512 | GGTGGAATAGTCCCA[C/T]CTAAGTCACATAATC | 10533 |
| rs75997856 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11373639 | AGGTCACGGTGAATT[C/T]TTCTCCACCCAAGCA | 10533 |
| rs76001986 | in-del | -/CCAAAAAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411618 | AGCAAGACTCTGTCT[-/CCAAAAAAAAA]AAAAAAAAAAAAAAA | 10533 |
| rs76027522 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509407 | TGGTTTTTTTTTTTT[-/TT]AAGTGCCAAATTGTG | 10533 |
| rs76042545 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11370180 | AAAATGGAAACTTAT[A/C]CACTCTCCTAAAAAG | 10533 |
| rs76058789 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11514143 | TGAAAATATTAACAC[C/T]GCTCTTTTATAGGTA | 10533 |
| rs76065428 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297499 | TTTCTTTAGTATTGT[C/T]CTTCTCAAACTGGGG | 10533 |
| rs76087835 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11467967 | CAGTAGCTGACTTGG[A/G]AACTGGGCAGAGTTG | 10533 |
| rs76089944 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11489910 | aagtatgtggtcaat[G/T]ttggaataggtgtgg | 10533 |
| rs76094242 | snp | C/G | 0.105214 | 0.203807 | intron-variant | ATG7 | GRCh38.p7 | 3:11393709 | TTCTTTTATCTCAGT[C/G]TCATTCGGTTGCCCA | 10533 |
| rs76106230 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | ATG7 | GRCh38.p7 | 3:11383356 | TGTTTCCCTATGATT[C/T]GATTCAGGTTATGAA | 10533 |
| rs76113546 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11472524 | CCACCTAAGTCACAT[A/G]ATCTGAGAGCCAGGG | 10533 |
| rs76116306 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531867 | GAGACCCTGTCTCAG[A/G]AAAAAAAAAAAAAAA | 10533 |
| rs76118811 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | ATG7 | GRCh38.p7 | 3:11393326 | GCTGTAGCTGATGCT[A/T]TTGTAATAGCCACAC | 10533 |
| rs76128708 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11463503 | TCCCATCCCAATTCA[C/T]GTCAGCCCTTCCCGC | 10533 |
| rs76154610 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | ATG7 | GRCh38.p7 | 3:11351616 | AGCCTCTTCCTTCAC[A/G]CTTACATTGTGTTAC | 10533 |
| rs76176610 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11443369 | AAGCACCATGCATGT[C/T]TGAGGTGGTTTCCTT | 10533 |
| rs76200378 | snp | A/G | 0.181978 | 0.240568 | intron-variant | ATG7 | GRCh38.p7 | 3:11506109 | TGAGTTGGTCTCTCT[A/G]TAAATGTGCCTTCTT | 10533 |
| rs76203973 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11393695 | TGTAGGTTTTTTTTT[C/T]CTTTTATCTCAGTCT | 10533 |
| rs76230113 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11292039 | CAAAGGCAGTGACCC[A/G]TGAGTATATCACTGC | 10533 |
| rs76289547 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11392475 | AAAAAAACAAACAAA[A/C]AAAACAAAACAAAAC | 10533 |
| rs76305702 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11416846 | TCAGTGATACAGATT[A/T]CTGTCTCTAAGCATT | 10533 |
| rs76351240 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ATG7 | GRCh38.p7 | 3:11523158 | AACATCCCCAGGTTG[C/T]AAGGATTAGTCAGAA | 10533 |
| rs76351372 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11529337 | ACATTTAGGAACCGT[A/G]ACACAAGAGAAGCTG | 10533 |
| rs76377240 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298510 | AATAATCAAGATGGT[A/G]AAGTATATGTTATGT | 10533 |
| rs76439720 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11539728 | GAATTTAAAAAATAA[A/C]ATCTATTGATGCGCA | 10533 |
| rs76443062 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11311305 | CCTGATAAAGTTTCT[G/T]AGAATTCGTGAGGTC | 10533 |
| rs76492392 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314427 | TTTTTGTTGTTGTTC[G/T]TACAAATCCGAGGTT | 10533 |
| rs76515840 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534126 | TTGGCACAGCCATGC[A/C]CCTTTGCCCAGGGCT | 10533 |
| rs76537624 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11514513 | GGAAATACCGCCCAG[G/T]CTTTTTACCCACCCT | 10533 |
| rs76538874 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11411632 | TCCAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs76540286 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11455371 | ATAATGTGGTTTAGA[G/T]TAGTCAGTTTCTGCA | 10533 |
| rs76540982 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | ATG7 | GRCh38.p7 | 3:11535054 | TATCCCTGCCCTTGC[A/G]GGTCACCTCCTCAGG | 10533 |
| rs76543081 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11357492 | CATACTCCTAAGTAG[A/T]TTTTTTGGCTCTAAG | 10533 |
| rs76546215 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11286527 | GGATATCTATAGAAA[A/G]TTCCTTGTTTTTGTT | 10533 |
| rs76581138 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | ATG7 | GRCh38.p7 | 3:11323579 | ATTGTCCCATTACCA[A/G]TCTTTTGGGGAAGGT | 10533 |
| rs76593305 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11286586 | CTTTCTTTCTTTCTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs76621023 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ATG7 | GRCh38.p7 | 3:11426430 | TTGACAAAATCCTTT[C/T]TCTCCTCCCTTCTCA | 10533 |
| rs76652346 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11415264 | ACCATAAATGGAGTT[G/T]GTAGGGCTGGAAGTT | 10533 |
| rs76656595 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409788 | TTCTTTTTTTTTTTT[-/TT]CCATGTGGTTGTCCA | 10533 |
| rs76668994 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500276 | TAGAATTTGGTTGGA[A/G/T]TAAGGAGGTGGAGAC | 10533 |
| rs76671440 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531845 | CTTCAGCCTGGGTGA[C/T]AAGAGTGAGACCCTG | 10533 |
| rs76674026 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11528830 | GACTCCATCTCAAAA[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs76677375 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11459996 | CTCTTACATGTCTCA[A/G]ATCGTACAGAGATTT | 10533 |
| rs76680218 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11402078 | TAATAACAGGGTGGT[C/T]GCAGGAGAATAGAAA | 10533 |
| rs76700699 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11545456 | CCTGCCTCCCATCCT[C/T]GGCTCCCGGCTGGAG | 10533 |
| rs76708041 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271763 | TTAATAGCAGTCATC[A/G]CTCTTGTTGTTATGA | 10533 |
| rs76715481 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ATG7 | GRCh38.p7 | 3:11403051 | CTGTAGTGATTACAA[C/T]GTTGAATAGTACACT | 10533 |
| rs76716636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11363034 | TTTACAGAGAATTTC[A/G]CTATTTCACCCTCAA | 10533 |
| rs76722452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472483 | TGGGATATATTCTTA[C/T]CTCTAGGGTTAGGGG | 10533 |
| rs76734637 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11355545 | CTTGTTTTTAAGGGG[G/T]AAAAAAGCTTGAACA | 10533 |
| rs76736714 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11481864 | GTAAGATGGGAGTGA[A/T]GGCCAAAGGCCTTTG | 10533 |
| rs76742669 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11410392 | AATTTGTCTTGTTGA[C/G]AAATGTACTTTATTC | 10533 |
| rs76776943 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11314416 | TGATTAAATTTTTTT[G/T]GTTGTTGTTCGTACA | 10533 |
| rs76787223 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11369280 | TTTCCTGAGATGCAG[C/T]CCAGGAAAGGAGCCT | 10533 |
| rs76796695 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11323324 | AGCCTGTATGGGCCA[A/G]CTCCAGCACAACACT | 10533 |
| rs76805294 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11441152 | GCTTTCAAGCATCTG[C/T]GTTTATCCTACCTTA | 10533 |
| rs76808658 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ATG7 | GRCh38.p7 | 3:11306067 | TCCACATCTGAATTC[A/G]TATTCAGAATCAACT | 10533 |
| rs76835738 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11546626 | AAATGGGACCCAAGT[A/T]TGAAATTGGATGATG | 10533 |
| rs76845042 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11289225 | AGGCAAGCCTTACTT[C/T]TTCAGGAAGTAGGTA | 10533 |
| rs76846933 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11311605 | GCAAGACTGTCTCCA[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs76859048 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11443450 | GAGTGCAGTGGCACA[A/G]TCTTGGCTCACTGCA | 10533 |
| rs76862735 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11405807 | TAATTTTTTGTAGAG[A/T]TGGGGTTTCGCTGTG | 10533 |
| rs76866660 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11429950 | GACTCTGTCTCAGGA[A/G]AAAAAAAAAAAAAAA | 10533 |
| rs76896147 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348805 | TTTTACAGAGTGCTG[A/C]TTGGTGCGTTTACAA | 10533 |
| rs76906744 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11363209 | GTGCTAGGCACTGTT[C/G]TAAGCACCTTAGAAA | 10533 |
| rs76931731 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11363681 | ATGGAAAAGCCAGGG[G/T]TTAGCTCAACCAGTG | 10533 |
| rs76949575 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534124 | AGTTGGCACAGCCAT[A/G]CCCCTTTGCCCAGGG | 10533 |
| rs76955931 | in-del | -/ATTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525058 | TTTATTTATTTATTT[-/ATTT]TTGAGACTGGCTCTG | 10533 |
| rs76967248 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11278082 | TTTGTCTTCCCTTTT[G/T]CCTTGAAAATCACTG | 10533 |
| rs76982575 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365878 | CTGCATGTTGGGAGA[G/T]TTTGCTTCCTGTTGG | 10533 |
| rs76988957 | snp | G/T | 0.00756529 | 0.0611122 | intron-variant | ATG7 | GRCh38.p7 | 3:11493372 | TTATAGACACAGGAT[G/T]GGGGGACAGGGCTGG | 10533 |
| rs77009041 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526485 | ATTTTTTAAGATGCT[A/C]ATTTATAAGCAATAG | 10533 |
| rs77015927 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11413689 | AAGTGGTATTAGTCC[A/C]TGGTTTTCTCATAGT | 10533 |
| rs77017001 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | ATG7 | GRCh38.p7 | 3:11353637 | TCTCCACATTAATGA[A/G]TGAGTTCTCGACCTC | 10533 |
| rs77023847 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531868 | AGACCCTGTCTCAGG[A/G]AAAAAAAAAAAAAAA | 10533 |
| rs77045548 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11424489 | CACCAACAACAACAA[A/C]AAAAACACTGATTGC | 10533 |
| rs77049999 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ATG7 | GRCh38.p7 | 3:11454345 | AAAATGCTTGGGTCA[A/G]AAATGGGCACATGAC | 10533 |
| rs77051956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11413098 | TGTACATGTAAAATC[A/G]TATCATTTGCAAGCA | 10533 |
| rs77075000 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | ATG7 | GRCh38.p7 | 3:11379232 | CTATGGAGAGTTTAG[A/C]GATGTTACCATTCAT | 10533 |
| rs77075989 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11403543 | CAAATGTAAACTTTT[A/C]TGTAGTTTTTAAGGT | 10533 |
| rs77076863 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11552962 | GCCCCGGCCCAGGCC[C/T]GAGTCCTCTTATGAA | 10533 |
| rs77077673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11457165 | GCTTACCCAAATGAG[C/T]GGAAAGATGCCAGGT | 10533 |
| rs77079537 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11498304 | CAATCAAGGGACACA[A/G]TTCCTGCTATCTGGG | 10533 |
| rs77088813 | snp | A/G | 0.110872 | 0.20771 | intron-variant | ATG7 | GRCh38.p7 | 3:11415032 | GTCCTTATACAAACC[A/G]TGACAGCATAAGCCT | 10533 |
| rs77090174 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11412328 | CTCAGATAAAACAAA[C/T]ATGAGTTTCAAGCTT | 10533 |
| rs77097128 | in-del | -/GTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314424 | TTTTKTTGTTGTTGT[-/GTT]TCGTACAAATCCGAG | 10533 |
| rs77111310 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11522840 | GTTTTGATTTAGTGT[C/T]TGAAGGCTTCCTTTC | 10533 |
| rs77116073 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11312189 | GTAAATTATATCTCA[A/G]TAAAAAGTCATCTAA | 10533 |
| rs77117351 | snp | G/T | 0.0744748 | 0.178019 | intron-variant | ATG7 | GRCh38.p7 | 3:11291154 | AGTTACATTTGTCCT[G/T]GAAGAGAAAGTTGTG | 10533 |
| rs77122928 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11408098 | TGAAACTGAATGCCT[G/T]TGACAGAACCCAAGT | 10533 |
| rs77135406 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309464 | TGATTTTTTTTTTTT[G/T]TTTTTTTAAAGACAG | 10533 |
| rs77149256 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11291000 | TCTGTTATCTTTTAA[G/T]TAGTCATCCTTAGTC | 10533 |
| rs77175900 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11384345 | GGACCTGCGCAGATG[C/G]AGCAAGATGTGCCCA | 10533 |
| rs77206639 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11340340 | CAGCAACTTCCAATA[A/G]CAGTGAAAGTTGAGC | 10533 |
| rs77207623 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | ATG7 | GRCh38.p7 | 3:11278483 | TCCCGCAACAGAACT[C/G]ATTTGTATTTTCTCA | 10533 |
| rs77235553 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11494143 | AGGCTTTAATCAGGC[A/G]CTGCAGCAGGCAAGA | 10533 |
| rs77236806 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11416928 | AGTTTAAATATTTTA[A/T]ATTTATCTTGAGATT | 10533 |
| rs77243949 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11361301 | CTTTTTTTTTTTTTT[G/T]TGAGACAGAGTTTCG | 10533 |
| rs77251970 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11537825 | AGATGTATTTTCCTG[C/T]GGGGAAACTGAGTCC | 10533 |
| rs77256485 | in-del | -/GC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501545 | ATAGATAATGATATT[-/GC]AATAGATAGGTGTGA | 10533 |
| rs77273496 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11333764 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 10533 |
| rs77286909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499309 | CTTGCTCTTATGAAA[C/T]GACTGCCAAAAACCC | 10533 |
| rs77302999 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ATG7 | GRCh38.p7 | 3:11443173 | CATACACACTTCTGT[A/G]TGGGGCGTGCTCCCA | 10533 |
| rs77308694 | snp | A/C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11433316 | AAAAAAAAAAAAAAA[A/C/G]CTGCGTTTGTTGAAG | 10533 |
| rs77327553 | snp | C/T | 0.127944 | 0.218179 | intron-variant | ATG7 | GRCh38.p7 | 3:11293698 | CTAAAAAATACAAAA[C/T]ATTAGGGCCAGGCAT | 10533 |
| rs77328700 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11545244 | CCCTCTGTGCAAGGG[G/T]AAGATTTTGAAGGCT | 10533 |
| rs77355520 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11413254 | TTTCCTGATCTTAGA[C/G]AGAAAGCGTTCCTTC | 10533 |
| rs77356414 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465051 | GGCTGTAAAGGAAAA[A/T]TTTTTTTTCTTATCA | 10533 |
| rs77367100 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11472996 | CATACTTTCCTTTCA[C/G]TTTTTTTTTGTAACT | 10533 |
| rs77367643 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11494668 | TAGATCATCTCTTGA[C/T]GGAACACAGATATGG | 10533 |
| rs77369937 | in-del | -/AAAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469989 | ACGAGACTCCATCTC[-/AAAAAAA]AAAAAAAAAAAAAAG | 10533 |
| rs77386855 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372707 | CTAAGGGAAAAAAAA[A/T]GTAATGGAAATCTTA | 10533 |
| rs77402512 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531746 | GCACATGTCCGTAGT[C/T]CCAGCTACTCGGGAG | 10533 |
| rs77411757 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ATG7 | GRCh38.p7 | 3:11521441 | GACTGGGGAAAAGGC[A/G]CATCGCACAGCAGGG | 10533 |
| rs77412764 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | ATG7 | GRCh38.p7 | 3:11522780 | ATGCCCACCCCAGGC[A/C]TAGACTGCTCTGAGC | 10533 |
| rs77419935 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ATG7 | GRCh38.p7 | 3:11500681 | AGACGGAGTTTTGCT[C/T]TTGTTACCCAGGCCG | 10533 |
| rs77422734 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ATG7 | GRCh38.p7 | 3:11522755 | CGTAACCTTCAAAAT[C/T]GCCTGTCAAATGCCC | 10533 |
| rs77437870 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439918 | TTAGGAGGTGACTAT[A/T]ATCCCATTTTATGGA | 10533 |
| rs77439194 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11538242 | GCACTGCCCTCTCAA[C/T]GCTGACCTGTCAGCT | 10533 |
| rs77483848 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11295799 | CTTTCTTTTTTTTTT[G/T]TTTTGAGATGGAGTT | 10533 |
| rs77492374 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11317601 | TTTTTTTTTTTTTTT[G/T]TTTGTTTTTGAGGCA | 10533 |
| rs77499826 | in-del | -/TATTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525054 | TTTATTTATTTATTT[-/TATTTT]ATTTTTGAGACTGGC | 10533 |
| rs77512352 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11528008 | ATCATTAAATCTTCC[C/T]TGCTTTGCCTGTTAC | 10533 |
| rs77525610 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336697 | TTTTTGAGACAGGGT[C/T]TTGACCTGTCACCCA | 10533 |
| rs77532959 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534125 | GTTGGCACAGCCATG[C/G]CCCTTTGCCCAGGGC | 10533 |
| rs77547639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343950 | AGTTCTGGGAGCATG[G/T]TGTATCTCTTAATTA | 10533 |
| rs77548310 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287429 | GGGCTGTGAGTTCTA[G/T]GCCATGGGGGCCTGA | 10533 |
| rs77562117 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11342767 | CAGATTACTTTCTAT[A/T]TTTTTCTATTAGATA | 10533 |
| rs77575555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11364565 | AGGGGCATTTTAGTT[A/G]TCCTTATGAATCTTA | 10533 |
| rs77622476 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11318586 | AGTGCATTTTCTAAC[A/G]TGTAAATTTGATCAT | 10533 |
| rs77642304 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11303943 | AAAAAAAAAAAAAAT[A/T]AGCCGGGCGTGGTGG | 10533 |
| rs77688123 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11306747 | ATAGGGAATATATAG[A/G]CTTTTAGGGGGGAAT | 10533 |
| rs77688600 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271807 | TATCAGAGTTAATTT[C/G]TGAAAGGCCTTACAG | 10533 |
| rs77715734 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ATG7 | GRCh38.p7 | 3:11300801 | TACCTGAGATATTCA[A/G]CACTTTATTATGGAA | 10533 |
| rs77716631 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11346031 | TTACCAATTAACATG[C/T]CATTAAAAATGATGC | 10533 |
| rs77718218 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11397779 | ATGATTTATAATCAC[-/A]AGTAGAAAATTTTAA | 10533 |
| rs77776627 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458529 | CGGCATCCCAAAGTG[A/C]CGGGATTACAGGCAT | 10533 |
| rs77791763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531756 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 10533 |
| rs77795008 | snp | C/G | 0.104504 | 0.2033 | intron-variant | ATG7 | GRCh38.p7 | 3:11535810 | CATTTCAGAACTCCC[C/G]TGGACCTGCCAGCTT | 10533 |
| rs77795420 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11506013 | TATCACGTAAAGTCA[C/T]GTATTCATATATGGG | 10533 |
| rs77803380 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11403689 | TTTAGAAATTAATAC[A/G]AATGCTAATGAAAAG | 10533 |
| rs77827216 | snp | C/G | 0.106278 | 0.204558 | intron-variant | ATG7 | GRCh38.p7 | 3:11405923 | GTAATCCCACTGCAC[C/G]TGGCCATGTGTAGCA | 10533 |
| rs77835761 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487639 | CTGGCCAGGCGGGGG[G/T]CTGACCCCCCCACCT | 10533 |
| rs77843565 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11333213 | AAAGTACAACTTGTA[A/C]CTCTTTGCCAATGCA | 10533 |
| rs77848110 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11278041 | GGCTGTATTCTGCCT[C/G]ACCCCGCAGGCAGTC | 10533 |
| rs77863890 | in-del | -/GGA | 0.186869 | 0.243137 | intron-variant | ATG7 | GRCh38.p7 | 3:11463622 | TGAATTATCATAGGT[-/GGA]GGAGAGTGTTGGAGC | 10533 |
| rs77872841 | snp | G/T | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11445399 | ATCATGGATGGAGCT[G/T]GAGGCCTTTATCCTT | 10533 |
| rs77873229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468644 | CCCTAGAAAGAGGAA[A/C]TCTTGATCCCCCACT | 10533 |
| rs77876296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11545732 | GTCAGCCCCCCTGGC[A/G]GTTCTTCCTTGGAAT | 10533 |
| rs77903059 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11366558 | CTTTCCCAAGTCTCC[C/T]GCCTTCTTCTGACCT | 10533 |
| rs77907666 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11534798 | GAGGCACCTGGCCAC[C/T]TTGGGACTGCACAGC | 10533 |
| rs77928941 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11422434 | CTCTGCTAGCTTCCA[A/C/G]CTGTGCCTCTGTAGC | 10533 |
| rs77990362 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11323095 | CAGAATGAAACTGTC[A/C]AAAAAAAAAGTTAGA | 10533 |
| rs77992000 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | ATG7 | GRCh38.p7 | 3:11505190 | TACTCAAGTGAAAAC[A/G]TTTTAAAAAGAACAA | 10533 |
| rs77995580 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531812 | GAGGCTGCAGTGAGC[C/G]CAGATCCTACCACTG | 10533 |
| rs77996146 | snp | A/G | 0.0607341 | 0.163335 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282394 | GCTTGTTCCCTGGTT[A/G]ACACACTGAAGAAGA | 10533 |
| rs78002645 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11553630 | CTGGTCACTGGACCG[C/T]AGACCGGCCCATCCA | 10533 |
| rs78061508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423629 | AATGCCTTTTTTTTT[C/T]CCAGGGGGTTAGGCT | 10533 |
| rs78066385 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372845 | GTGTGTGCGTGCGTG[C/T]GTGTGCGTGTGTGTG | 10533 |
| rs78075374 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11528825 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs78084377 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531811 | TGAGGCTGCAGTGAG[C/T]CCAGATCCTACCACT | 10533 |
| rs78085574 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ATG7 | GRCh38.p7 | 3:11492955 | TCCATGGACAGCAGC[A/G]TGTTATCAGCTTAGT | 10533 |
| rs78122142 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11457166 | CTTACCCAAATGAGC[A/G]GAAAGATGCCAGGTT | 10533 |
| rs78155279 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11279820 | CTATAACATTCTGTA[C/G]AAACGCCAGGCTATA | 10533 |
| rs78175084 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413197 | GCTAGAACTTCTAGT[A/T]CTGTGTTGAATAGAA | 10533 |
| rs78184606 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ATG7 | GRCh38.p7 | 3:11382863 | CTCCGGTATACACTT[C/T]ACCCACATTCATCCA | 10533 |
| rs78192877 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11355993 | AATGGAATGTATTAT[G/T]GATACTTAACAATAT | 10533 |
| rs78215819 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11381058 | TTTAGATGCTCAAAA[A/G]TTGAGACTAATTATT | 10533 |
| rs78221330 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487507 | GGCGGCTGGCCGGGC[A/T]GAGGGGCTCCTCACT | 10533 |
| rs78231359 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11423251 | TTTATCTATTAAGGT[C/T]GCCATCTTATATAGG | 10533 |
| rs78247474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11314460 | GGTTTTGTGGAACTA[A/G]TTTCCCAAGAGGAAA | 10533 |
| rs78250516 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11517932 | TTCAGAAAGATGGGC[A/T]CAGTGTGAGGGATGG | 10533 |
| rs78262792 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ATG7 | GRCh38.p7 | 3:11409368 | CTCAACCACACGATC[A/G]TGAGGGTAAACAACT | 10533 |
| rs78273652 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ATG7 | GRCh38.p7 | 3:11444525 | GCATACTGTAAGTTA[C/T]TTATCTCATACTAGA | 10533 |
| rs78309102 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | ATG7 | GRCh38.p7 | 3:11547465 | TTTATGAATACTTTC[C/G]TATGAATACTACTGT | 10533 |
| rs78310323 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | ATG7 | GRCh38.p7 | 3:11341807 | AAATTTCTGTTTTCA[G/T]TACTAGGAAAAACTT | 10533 |
| rs78314392 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11354079 | TATCCCAGACTAACC[A/G]TATTCTGGCCCCAGA | 10533 |
| rs78323416 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11375057 | AAAAAAAAAAAAAAA[A/T]CAAAAGAATTAGCTG | 10533 |
| rs78325664 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11310648 | AGTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTC | 10533 |
| rs78337551 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531798 | GAGCCCAGGAGGTTG[A/T]GGCTGCAGTGAGCCC | 10533 |
| rs78351290 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11476418 | CTTTATGTGGTTTTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs78366132 | in-del | -/GAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11463625 | ATTATCATAGGWGGA[-/GAG]GAGTGTTGGAGCATT | 10533 |
| rs78377196 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11544715 | GGCCCGCCCTTGACT[A/G]TGTGTGTCTCAGGTA | 10533 |
| rs78427473 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11296923 | CTAACTTTGTATTTC[A/C]TTATACAGTTTCTAT | 10533 |
| rs78456022 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11453417 | AAGAAGATTATTTCC[C/T]GCCGTGGCTGTCCCT | 10533 |
| rs78463118 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11310912 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCATGC | 10533 |
| rs78485478 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341797 | GATATGGGAGAAATT[A/T]CTGTTTTCAGTACTA | 10533 |
| rs78498684 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11498631 | CTGGTGCTCCAAGAC[A/C]TGCTGGCCAGACTGG | 10533 |
| rs78505701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11464966 | CATAGTAAACACTCA[A/G]CAGATGCCACATCTA | 10533 |
| rs78563559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11383196 | AGGATCCAGTTGAGG[A/T]TCAAACATTGCATTT | 10533 |
| rs78594398 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11480028 | CGTCTCTGGGGTTCA[C/T]GACATTCTCCTGCCT | 10533 |
| rs78602284 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11466768 | GCATCAGAATGACAG[C/T]TTGTAGTACACTCAT | 10533 |
| rs78602883 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271678 | TCTTTCATATATAAC[G/T]TGGGGATATGTTTCA | 10533 |
| rs78619498 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11374509 | ATAAATCTTTATGAA[C/G]TTGGATTAGACAATG | 10533 |
| rs78622260 | snp | C/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487685 | CGGCTGGCCAGGCGG[C/G]GGGCTGACCCCCCCA | 10533 |
| rs78638774 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | ATG7 | GRCh38.p7 | 3:11505628 | AGACCACTCTCAGCC[C/T]TCAAGGGTCCTTGCA | 10533 |
| rs78667716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310250 | ATTTTACTTCTTTAG[A/T]ATAAGTTCTTTGGAG | 10533 |
| rs78668498 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11424769 | TTCTGCCAGAGATAT[C/T]CTTCCATAGATGATA | 10533 |
| rs78681093 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11514530 | TTTTTACCCACCCTC[A/C]GCCACCCCATGCACT | 10533 |
| rs78691822 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531832 | TCCTACCACTGCACT[C/T]CAGCCTGGGTGACAA | 10533 |
| rs78694752 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434813 | AGAAAGAAGGGGGGA[A/G]ATCATAAATGCTGAA | 10533 |
| rs78696987 | snp | C/G/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11467374 | ACCTCAACCGTAATT[C/G/T]GTTTTGTTTCGTTTT | 10533 |
| rs78724985 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11441684 | AATTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 10533 |
| rs78726015 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11492529 | TTTGCTGAGGGACTC[C/G]TGACAGGGGTTCCCT | 10533 |
| rs78779519 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11518667 | GGAGATGGACATCTG[C/G]GAGTTGCTGGATTCT | 10533 |
| rs78784111 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11381022 | TAGAATTGACAAGCA[A/G]TGTTGATAAATTTGG | 10533 |
| rs78792196 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | ATG7 | GRCh38.p7 | 3:11329835 | AGCTCTAGACATTTC[C/T]GATTTCACCAGTTTT | 10533 |
| rs78831006 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11482747 | GATATCTAGTGCCAG[C/G]CTACTAATCCAGTGC | 10533 |
| rs78835760 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11499863 | CTAGCTGTTACACAG[C/G]TGTAGTATCATACCA | 10533 |
| rs78851569 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11402806 | TTTTTTAATGGAGTC[A/T]GGGTCTCATAGCCAC | 10533 |
| rs78869324 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ATG7 | GRCh38.p7 | 3:11549538 | GCTTCCTTGACCCAG[A/G]ATAAAGACACTGAGA | 10533 |
| rs78891930 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11536650 | GGGAGTCCCGAGAGC[A/G]GACCCTCTTGCCACT | 10533 |
| rs78893413 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11378994 | GTTGAAGACAAACGC[G/T]GTGGTATTCTGAGAG | 10533 |
| rs78903403 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11289664 | GTGGGCTCGAGCTAT[C/T]TTCCTACCTCAGCTT | 10533 |
| rs78917526 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11311606 | CAAGACTGTCTCCAA[A/C]AAAAAAAAAAAAAAG | 10533 |
| rs78927830 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11448559 | ATCTGTAATCAGGAA[C/T]ATAAACCAACACAAT | 10533 |
| rs78927846 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11446264 | TAAATTGGATTAAAG[G/T]TTACTATATCCATTT | 10533 |
| rs78957588 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11411978 | TTCAAAAGACTGTCC[C/T]TTTTTTTTTTACTGA | 10533 |
| rs78983796 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288289 | ACTGCTGAAATTTAT[C/T]TTACTATATAGCATC | 10533 |
| rs79031426 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11539818 | GGAACCAGCACAGTT[C/G/T]GGCGACATCGAGCAG | 10533 |
| rs79031568 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11487564 | CGCCCCTCACCTCCC[A/G]GACGGGGCGGCTGGC | 10533 |
| rs79060073 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11323714 | TCTGTGGACAAGAGC[A/G]ATAGCCAAGGAGCAA | 10533 |
| rs79069652 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11281774 | AGCGAAACTCCATCT[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs79076247 | snp | G/T | 0.277778 | 0.248452 | intron-variant | ATG7 | GRCh38.p7 | 3:11543560 | GTACAAGAGTGGGAA[G/T]GCAGGCGGGTGTCTT | 10533 |
| rs79080411 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526552 | TCAAAGTGGTTATTA[C/T]TGGTGTATAGCAAAA | 10533 |
| rs79086200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272845 | CCATCTGCAAAATGG[G/T]AATGATAATCCGCCA | 10533 |
| rs79094614 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531874 | TGTCTCAGGAAAAAA[A/G]AAAAAAAAAAAAAAG | 10533 |
| rs79124042 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | ATG7 | GRCh38.p7 | 3:11355489 | TCTTATCCAGAACAC[A/G]CAAGATGAACAACTC | 10533 |
| rs79129776 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11412461 | TCAAAAATTGAGACT[A/G]TATCTGTGAGGATTG | 10533 |
| rs79129919 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11338906 | TAATTATATTGGGCA[A/G]TACTATTTTTTTAAA | 10533 |
| rs79133212 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11359539 | CTCTCTAGAAGAAAA[A/C]CAAAAAATTAGCTAG | 10533 |
| rs79140218 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11352244 | ATTTTCTTAATCCAG[C/T]CTATCATTGATGGAC | 10533 |
| rs79154253 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11486854 | TTAATTTATTTTTTT[A/T]TTGATAATTCTTGGG | 10533 |
| rs79163198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400265 | AAGTTTTCAATAATT[G/T]ACCCACCCACACCAT | 10533 |
| rs79166175 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | ATG7 | GRCh38.p7 | 3:11508779 | TTTGAACTAATAATC[C/T]TCAGTTCTGTGCCTG | 10533 |
| rs79170563 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11444420 | GCTGAGCTTTGGAGA[A/G]CCACTAAACACTGTC | 10533 |
| rs79173265 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11349356 | CCAGCCTGGGAGACA[C/T]AGTGAGACCCTATCT | 10533 |
| rs79188637 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273314 | CCCACTGGCCAGATT[G/T]CTTCAGTGACAGAAA | 10533 |
| rs79199187 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486816 | GGTTTTTGTCTTTGG[C/T]TCTGTTTTTTTTTTT | 10533 |
| rs79205509 | snp | C/G | 0.105924 | 0.204309 | intron-variant | ATG7 | GRCh38.p7 | 3:11399074 | AGATGCAGGCTGGGC[C/G]CAGTGGCTCACGCCT | 10533 |
| rs79216182 | in-del | -/TTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11476431 | TTCTTTTTTTTTTTT[-/TTT]GGTTTTTCCTTAGAT | 10533 |
| rs79217567 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11493110 | ATGAGGTCACGTAGA[C/T]GAATTGAAGTTATGG | 10533 |
| rs79283992 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11518545 | AGCGAGACACCCTCT[A/C]AAAAAAAAAAAAGAA | 10533 |
| rs79290281 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ATG7 | GRCh38.p7 | 3:11412736 | AACACCGTTGGATTT[A/G]TATAGAGATCACAAT | 10533 |
| rs79296546 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11455237 | TTCATGAAGCAAGTT[A/G]TTGATTTTAAGTAGA | 10533 |
| rs79324744 | in-del | -/TTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459509 | AAGTGTTTTTTTTTT[-/TTT]AAGTGATTATGTTAG | 10533 |
| rs79336807 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11540954 | GCCCAGGCTGGAGTG[C/T]AGTGGTGCAATCTTG | 10533 |
| rs79337214 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11413248 | TGCCTTTTTCCTGAT[A/C]TTAGAGAGAAAGCGT | 10533 |
| rs79370386 | snp | A/G | 0.093777 | 0.195178 | intron-variant | ATG7 | GRCh38.p7 | 3:11541897 | CTCAATAACCATTTC[A/G]TTTAAAATGTGGGCC | 10533 |
| rs79415158 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ATG7 | GRCh38.p7 | 3:11326176 | TAAGCAAGTGAGTTT[C/T]TCACTACATCAGGCC | 10533 |
| rs79420214 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531813 | AGGCTGCAGTGAGCC[C/G]AGATCCTACCACTGC | 10533 |
| rs79444831 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11539039 | CTGGCTGTAATACAA[A/G]GTCGATTACCCACAG | 10533 |
| rs79470496 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11372833 | GCGCGTGTGCGTGTG[C/T]GTGCGTGCGTGCGTG | 10533 |
| rs79487717 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11336560 | ATAAAGAATTTTTCT[A/G]TATCATAATGTAAAC | 10533 |
| rs79531179 | snp | C/T | 0.141596 | 0.225274 | intron-variant | ATG7 | GRCh38.p7 | 3:11384622 | TTTATTTTTTTGATA[C/T]TATATAATCCTACCT | 10533 |
| rs79543581 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11529074 | TGGAAAAAAGGGGGC[G/T]GTACATTCAGGTGAC | 10533 |
| rs79551744 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11278125 | TTTTCAAGGTGCACT[A/G]ATTTCACATTGTTCA | 10533 |
| rs79566921 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11404788 | GCAGACAAGGGCTTG[A/T]GGAGGGGAACTCCCT | 10533 |
| rs79567402 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11282944 | CATGTGGTTTGGTGC[C/T]TATTTTAATGACTGC | 10533 |
| rs79571088 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ATG7 | GRCh38.p7 | 3:11500177 | CAACATAAAGAACAA[C/T]ATGAACACAGTTGTA | 10533 |
| rs79585821 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | ATG7 | GRCh38.p7 | 3:11296341 | CATTCTCCTAGCCAT[C/T]TGTGGCTTGACACCC | 10533 |
| rs79597044 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11420771 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCT | 10533 |
| rs79603268 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11541340 | AAGATTGTCCTTTCT[C/T]GTCAAATTACTGTGC | 10533 |
| rs79606646 | snp | C/G | 0.104504 | 0.2033 | intron-variant | ATG7 | GRCh38.p7 | 3:11535745 | AACCTTGTGTTCTCA[C/G]TCTTAGGAGAGCTGT | 10533 |
| rs79615541 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | ATG7 | GRCh38.p7 | 3:11291396 | GTTCCTGAAAAGAAG[C/T]TTCTTCCTTCAAGGC | 10533 |
| rs79623147 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11494513 | TGGGACAGCTGGGCC[A/G]GTTTCAATGGGCTGT | 10533 |
| rs79629947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11505285 | AATGGAGGAGTGTTC[A/G]CGCAGGTAGAGAAAA | 10533 |
| rs79644793 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11361288 | TTAATAATGAATTCT[C/T]TTTTTTTTTTTTTTG | 10533 |
| rs79670324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11372542 | ACTCACATAACTATC[A/G]CTTCCACAAATGAGA | 10533 |
| rs79691366 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11532720 | AGAGTGAGACCTGTC[A/G]TAAAAAACGAAACAA | 10533 |
| rs79717556 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390759 | ATTTTTAAAAAACTG[C/T]AAGTTAAAGTACTGC | 10533 |
| rs79722471 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458536 | CCAAAGTGCCGGGAT[G/T]ACAGGCATGAGCCAC | 10533 |
| rs79779397 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348784 | CTCTATAAAATGGAC[A/C]AGTCAGCACTTTGTA | 10533 |
| rs79780788 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531821 | GTGAGCCCAGATCCT[A/G]CCACTGCACTTCAGC | 10533 |
| rs79785454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402988 | AAACCAGGAATCTAT[C/T]CTCTTAAATGCTTAA | 10533 |
| rs79785758 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11506217 | ACCCCAGAATATCAC[A/G]GTTTAAACATGGTAG | 10533 |
| rs79819250 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ATG7 | GRCh38.p7 | 3:11536192 | GATTGGAGGAGAACC[A/G]AGAGGTTTTCAGTAG | 10533 |
| rs79840802 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11284862 | GCCTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTT | 10533 |
| rs79845222 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11283753 | GACCAGCCTGGCCAA[A/C]AAAGCAAAACCCTAC | 10533 |
| rs79845471 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11514531 | TTTTACCCACCCTCA[A/G]CCACCCCATGCACTA | 10533 |
| rs79875606 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11429951 | ACTCTGTCTCAGGAA[A/G]AAAAAAAAAAAAAAA | 10533 |
| rs79880623 | snp | C/G | 0.0722614 | 0.17581 | intron-variant | ATG7 | GRCh38.p7 | 3:11323514 | ATTGCTACAACAGAT[C/G]ACCATCTTTCAGGCC | 10533 |
| rs79885194 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11377210 | GAGAAGAAGGGTTTC[C/G]TGTCTTGAATTATCT | 10533 |
| rs79912060 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11459274 | CTACATGAGATTTGC[C/T]CTGATTCATAGATGG | 10533 |
| rs79914825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522159 | CCCAAGCATTACAAG[C/G]TTATTCTTGGGAGGA | 10533 |
| rs79941725 | snp | C/T | 0.00389734 | 0.0439714 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331420 | TTTGGTCCTAGCAGC[C/T]CACAGATGGTATTTA | 10533 |
| rs79978351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473157 | TGGTGAGGAATAATA[A/G]AACATTATAGCACTT | 10533 |
| rs79979667 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11531846 | TTCAGCCTGGGTGAC[A/G]AGAGTGAGACCCTGT | 10533 |
| rs79994656 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11393085 | GGCGCAGGTGATGGA[A/G]TCCTCTGTTAAGTGT | 10533 |
| rs80009021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11280324 | CTATGGGCCAGATGT[A/G]TGCATTTTCTAGTTG | 10533 |
| rs80010634 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11394433 | TCTGAGTTGAGCTTT[A/G]AGAGAGAATGTAAGC | 10533 |
| rs80039262 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11310395 | CCCCGACCTCCCACC[A/G]TTCCTCCTAGATTCC | 10533 |
| rs80068344 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11542261 | ACACTCCAGGAGAGA[C/T]CGTGTAGATATTGGT | 10533 |
| rs80068819 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ATG7 | GRCh38.p7 | 3:11381901 | AGATTGTCATTCTCT[A/G]TTATCTGCAAACCCA | 10533 |
| rs80070250 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11320165 | TCTTTACTTCTACCC[C/T]TCCCTCCCCCTACCT | 10533 |
| rs80098964 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11471747 | GCTTTTTAGATTTCT[C/T]TTTTTTTTTTTTTTG | 10533 |
| rs80124235 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ATG7 | GRCh38.p7 | 3:11476856 | TTGATCAAAACATGA[C/T]TCCACTCCCTTGTTT | 10533 |
| rs80131190 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11430179 | TTTCTTAACTCTGAA[C/T]AGGACTGTGTTTTAA | 10533 |
| rs80133740 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414002 | ATCTAGGTTATGGTA[A/T]TAGGTTTGTAATTTC | 10533 |
| rs80135182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11495136 | CAAACCTGACAGTCT[A/G]TGACTGCTTATGTGC | 10533 |
| rs80169326 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | ATG7 | GRCh38.p7 | 3:11283495 | AGGTGCAGGGGGGTG[A/G]AGGAACCTGCCCTAA | 10533 |
| rs80191019 | snp | A/G/T | 0.00478244 | 0.0486902 | intron-variant | ATG7 | GRCh38.p7 | 3:11512417 | GTACATCCACTCTCT[A/G/T]AGCTTTGGTTCTGTC | 10533 |
| rs80195697 | in-del | -/TTTC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501550 | TAATGATATTAATAG[-/TTTC]ATAGGTGTGATAATG | 10533 |
| rs80232732 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474403 | TCAGGAGTTCGAGAC[C/T]AGCCTGGGCAACATG | 10533 |
| rs80234821 | snp | C/T | 0.12932 | 0.218944 | intron-variant | ATG7 | GRCh38.p7 | 3:11316008 | ATAGGTGTGAGCCAC[C/T]GTGCCCAGCCAATAC | 10533 |
| rs80235772 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11518546 | GCGAGACACCCTCTC[A/C]AAAAAAAAAAAGAAA | 10533 |
| rs80274266 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11351531 | AGAAGGCTGAGGTGG[A/G]AGCAAGGGACGCCAT | 10533 |
| rs80275158 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ATG7 | GRCh38.p7 | 3:11546474 | ACTGCGCCCAGCCTT[A/G]TTTTAAATGTTTACA | 10533 |
| rs80280444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11379569 | ACCCAAAATCATGTC[A/G]TAGAAATGTGTATTT | 10533 |
| rs111232659 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11480315 | TGAGGTGGGAAGATC[G/T]CTTGAGGCCAGAAGG | 10533 |
| rs111236724 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11497341 | ACATAGTGAAACCCC[A/G/T]TCTGTACTAAAAATA | 10533 |
| rs111261379 | snp | C/T | 8.28329e-05 | 0.00643503 | intron-variant | ATG7 | GRCh38.p7 | 3:11554795 | CTCGGCTGAGCCTCT[C/T]CCCTTCTCCATGCAG | 10533 |
| rs111270666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11350229 | GGTTTAACAGTATTA[A/G]TTGACCACCCACTGT | 10533 |
| rs111287877 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11404172 | GAGTCTTGCTCTGTC[A/G]CCCAGACCGGAGTGC | 10533 |
| rs111290325 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11414871 | ATTGATTTTCAAATG[C/T]TGAACCAGGCTTGTG | 10533 |
| rs111292012 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11541259 | TTTCATGTAGGGTAT[G/T]AGTTAAGGGTGAAAG | 10533 |
| rs111293299 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ATG7 | GRCh38.p7 | 3:11423089 | ATTTAAAGTGAGAAA[C/T]GTGTGACTCTTCCTT | 10533 |
| rs111309441 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11305424 | AAGAAGGGTACCTTC[C/G]TCTTCTGTGCTTGTG | 10533 |
| rs111314299 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488724 | TGATTTGCATATATT[A/G]AACCAGCCTTGCATC | 10533 |
| rs111316032 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11316369 | CCCCTTCCCGTCAGA[C/T]ACATCTAAAACTTTT | 10533 |
| rs111322650 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | ATG7 | GRCh38.p7 | 3:11277962 | TTCTTGCTAGGAAAA[G/T]AATTTAGTGATATCT | 10533 |
| rs111325678 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11300864 | CTAGGCTAATGTAAG[C/T]GTTCTGGGCACGTTT | 10533 |
| rs111331016 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11408258 | AAAGCCACCTTTGTT[C/T]CAGTTCCCAACAAGT | 10533 |
| rs111332679 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11452363 | ACACCCCAGTCTGGG[C/T]GACAGAGCGAGAACC | 10533 |
| rs111335614 | in-del | -/A | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11310165 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAATAC | 10533 |
| rs111339979 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11476688 | TATTTTATTTTAGCC[A/G]AGTATTCTTGTCCAA | 10533 |
| rs111344199 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11479050 | CACACAATTTTTTAC[C/T]TTGTGGATACTGGCC | 10533 |
| rs111362668 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11551763 | GGTTCTTTTCTTTTC[-/T]TTTTTTTTTCTCGAG | 10533 |
| rs111368123 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11320240 | CTGACCTCTATAAAA[A/C]GGTTTATTCCTTCTG | 10533 |
| rs111370071 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11330980 | AGCAATTTTCACAGA[A/T]TATATTTCTTTGTTT | 10533 |
| rs111371108 | snp | A/G/T | 0.00478244 | 0.0486902 | intron-variant | ATG7 | GRCh38.p7 | 3:11308804 | GAAGGGAGTGTGGCT[A/G/T]GGAGAGAGGCAGTGT | 10533 |
| rs111373406 | snp | C/G | 0.0715223 | 0.175059 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272454 | GCCGCGGCGGGCGAG[C/G]GTGTAGTGGGGTCTT | 10533 |
| rs111389100 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11469629 | GCTCAGGAGTATTGA[C/T]GTTCCTCTTCTCAGT | 10533 |
| rs111397932 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11278475 | CCGTGACTTCCCGCA[A/G]CAGAACTCATTTGTA | 10533 |
| rs111405275 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | ATG7 | GRCh38.p7 | 3:11290962 | GCTGGGATTACAGGC[A/G]TGAGTCACTTCACCC | 10533 |
| rs111406472 | snp | C/T | 0.196149 | 0.244131 | intron-variant | ATG7 | GRCh38.p7 | 3:11503723 | ATCACGCCATTGCAC[C/T]CCAGCCTGGGCAACA | 10533 |
| rs111417596 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11410345 | ATTTTTTTTTAAATT[A/T]AAATTTGATAGTATT | 10533 |
| rs111420483 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11374701 | GTGAGGTCAGGAGAT[C/T]GAGACCATCCTGGTT | 10533 |
| rs111423374 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11362078 | TATAATATATAGCTG[C/G]TCTTGTTATTTAGTG | 10533 |
| rs111431769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11441575 | ACCAGTTTGGAACCA[A/G]TCTTTTAGAGGTAAC | 10533 |
| rs111441678 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11398776 | GGATTGCTTAAGCCC[A/G]GGAGTTTGAGCTTAT | 10533 |
| rs111442566 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11552298 | TTTAAAAAATATGGT[A/T]CCAATTTATACTTCT | 10533 |
| rs111456870 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | ATG7 | GRCh38.p7 | 3:11438514 | GAGGTTGCAGTGAGC[C/G]AAGATTGTACCACTG | 10533 |
| rs111484572 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11344594 | CATTTTGGCCGGGCA[C/T]GGTGGCTCACACCTG | 10533 |
| rs111501622 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451238 | TTTTTTTTGAGATCT[A/G]TATCACTCTGTCACC | 10533 |
| rs111508755 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11460425 | CCTGGCTCAGATGTC[A/G]TGAGAGAAGGGGTCA | 10533 |
| rs111518959 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | ATG7 | GRCh38.p7 | 3:11317795 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTAGTC | 10533 |
| rs111546807 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11354520 | TGGGCGTGGTGGCGC[A/G]CACCTGTACTCTCAG | 10533 |
| rs111546917 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11538521 | TATGGTAGAGAGGAA[-/AG]AGACTCATATTTGAA | 10533 |
| rs111550401 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11521907 | ATGACTCTAGACTGC[C/T]GCCGCTGCCGACAAC | 10533 |
| rs111556267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11378100 | CTCACTGCAACCTCT[A/G]CCTCCCAGGATCAAG | 10533 |
| rs111556766 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11540540 | CAGCTACTCAGGAGG[A/C]TGAGGTGGGAGGATC | 10533 |
| rs111567461 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11521558 | GGAAGGGTTTTTTTG[-/T]TTTTTTTTTTTTAAG | 10533 |
| rs111574991 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11389233 | GAGAGACCCTGTCTC[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs111590381 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11388433 | TGCTCATGTTCCTTC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs111595248 | snp | C/T | 0.0916144 | 0.193427 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270754 | TATAAAAGAACCTTC[C/T]TAAGGGTGGGGGAGA | 10533 |
| rs111595809 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11372071 | GTGAGGACGGTGTGT[C/T]CTGTCTCCTAAGGCC | 10533 |
| rs111599091 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492060 | GCGCCCCTCCCCCAG[C/G]CTCGCTGCCACCTTG | 10533 |
| rs111606543 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11456864 | CCTCTCTGAGGCCCC[A/G]GTATTGGAGGCTACT | 10533 |
| rs111608244 | snp | A/G | 0.136506 | 0.222754 | intron-variant | ATG7 | GRCh38.p7 | 3:11513559 | GCCTGCCAAGCCCAC[A/G]CCCACCCGGAACTCC | 10533 |
| rs111618869 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11363242 | TTGCCTCCTTCAATC[-/T]TTTTTTTTTTTTTTA | 10533 |
| rs111638761 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11337644 | AATGGCTATAGCCTT[C/T]ATTATTATTATTATT | 10533 |
| rs111642560 | snp | C/T | 0.0711817 | 0.174832 | intron-variant | ATG7 | GRCh38.p7 | 3:11303409 | GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 10533 |
| rs111643519 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11424991 | TTTTTTTTGTTTTTG[A/G]AGACTCTGTCACCCA | 10533 |
| rs111687873 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11529425 | AGATACGTGGCTTCA[A/C]ACAGAGAATTGTTTT | 10533 |
| rs111691175 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11537557 | ATTTCTTAGTCTCAG[A/T]TCCCATTTTCTCTCA | 10533 |
| rs111702050 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11521917 | ACTGCCGCCGCTGCC[A/G]ACAACAATAACAAAG | 10533 |
| rs111714834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555850 | AGCTTTTGTCTTAGG[C/T]CCAGAATCAAAGTGA | 10533 |
| rs111717745 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11381420 | TTTATGTTGGTCTGG[C/G]TAGTCAATGAAATAA | 10533 |
| rs111719969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298611 | GTTTGAATTAAACTT[C/T]ATTACAAATGTTCTT | 10533 |
| rs111720127 | in-del | -/AT | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11390335 | TAAGAAAACAAAAAC[-/AT]GTGTCTCCCAGCTCT | 10533 |
| rs111752053 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11418163 | AGGCTGGAGTGCAAT[C/T]GTGCGATCTCAGCTC | 10533 |
| rs111754082 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11432516 | AGCTTGGGAGGGGGG[G/T]TAAAGGATAAAAGAC | 10533 |
| rs111770158 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11311486 | GGCAGCCTGTAGTCC[C/T]AACTACTCGGGAGGC | 10533 |
| rs111771426 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11373968 | TTGTTTACTTGTTTA[A/T]TCATTTCATAATTTA | 10533 |
| rs111782118 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11283758 | GCCTGGCCAACAAAG[C/G]AAAACCCTACTAAAA | 10533 |
| rs111801998 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | ATG7 | GRCh38.p7 | 3:11348955 | GGTGCGTTTACAATC[C/T]TCCAGCTAGACACAG | 10533 |
| rs111806888 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11461353 | AGAAACCAAAGATAA[A/T]GTCACTTTGGAGCTA | 10533 |
| rs111823189 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11542880 | GTCTAGGTTCTGAGG[C/T]ATGAGACTGTTCCTT | 10533 |
| rs111824597 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11472997 | ATACTTTCCTTTCAC[-/T]TTTTTTTTGTAACTA | 10533 |
| rs111827101 | snp | C/T | 0.213062 | 0.248146 | intron-variant | ATG7 | GRCh38.p7 | 3:11546262 | CTGCAACCTCTTCCT[C/T]CCGGGTTCAAGCAAT | 10533 |
| rs111836722 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11377796 | CTCAAGCCTGTAACT[C/T]CCAGAGCTCGTGAAG | 10533 |
| rs111846771 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11399353 | ACACTGTCTCAAAAA[A/C]TAGAAAAATATAAAT | 10533 |
| rs111860920 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11479009 | ACACACACACACACA[A/C]ACACACACACACACA | 10533 |
| rs111870370 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11545822 | GTGCTCAGTAAGGGC[A/T]AGCAAACTAGCAGCC | 10533 |
| rs111871747 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11535954 | TGTGGGATGACGCAG[C/T]GTTGCCTGCCAAACC | 10533 |
| rs111880449 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11317632 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGAAGTAC | 10533 |
| rs111908774 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11475336 | ATTAATGTCACTTCT[C/T]ATAAAGGAGGAATCT | 10533 |
| rs111937999 | snp | A/C | 0.00637698 | 0.0561055 | intron-variant | ATG7 | GRCh38.p7 | 3:11372445 | ATTAAGATTATAAGC[A/C]TTTTTTAAAATCACC | 10533 |
| rs111943703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11437533 | TCTAAATCCCAACCT[A/G]GATCTGAATTTTTAA | 10533 |
| rs111950349 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11388058 | AAGCACCATTGCTCT[A/G]TGAGTGTTTCTTTGG | 10533 |
| rs111952938 | snp | C/T | 0.164219 | 0.234823 | intron-variant | ATG7 | GRCh38.p7 | 3:11385139 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 10533 |
| rs111964947 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | ATG7 | GRCh38.p7 | 3:11471863 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGATTAT | 10533 |
| rs111968075 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526689 | CTTTTGCAAATAACA[A/G]TAGTTTATACTCTTG | 10533 |
| rs111968419 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11523179 | TTAGTCAGAAGTCAT[A/G]ATGACTGTTCTATAT | 10533 |
| rs111973213 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11541145 | GACTTCGTGATCCGC[C/T]CGCCTCGGCCTCCCA | 10533 |
| rs111974898 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11541270 | GTATGAGTTAAGGGT[A/G]AAAGTTCATTTTTCT | 10533 |
| rs111980158 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ATG7 | GRCh38.p7 | 3:11315780 | TGCCTGGGCTGGAGC[A/G]CAGTGGCGCAATCTT | 10533 |
| rs111999785 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | ATG7 | GRCh38.p7 | 3:11393730 | CGGTTGCCCAGGCTG[A/G]AGTGCAGAGGTGCGA | 10533 |
| rs112001816 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11393260 | TCATCGGAAAAATTA[C/T]TTCTACCATCCTTTA | 10533 |
| rs112006666 | in-del | -/AGCGAGGCCAAACAACCATATAA | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11371968 | TGGGAACAGCCCGGG[-/AGCGAGGCCAAACAACCATATAA]AGCGAGGCCAAACGA | 10533 |
| rs112009342 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11415182 | AATGTATCTCAATAT[A/G]GAAAAAGTACAGTAA | 10533 |
| rs112015288 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11497154 | CCACGCCCAGCCCCT[A/G]ATGTCATTTCTGATG | 10533 |
| rs112019047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11335822 | CCAGACTCAGCCTCC[C/T]GAGTGGCTGGGATTA | 10533 |
| rs112020700 | snp | C/G/T | 0.00478244 | 0.0486902 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526118 | ATCAAGGGCCAGGCA[C/G/T]CATGGTTCATGCCTG | 10533 |
| rs112033889 | in-del | -/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11309460 | TGTTGATTTTTTTTT[-/G]TTTGTTTTTTTAAAG | 10533 |
| rs112048710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11352300 | TATTGTGAATAGTGC[C/T]GCAATAAACATATGT | 10533 |
| rs112057570 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11439999 | TTTACAGTACACTTC[A/G]TAAGGCTGGAATCAG | 10533 |
| rs112059892 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11447928 | GATGGGTGTTGGGCA[C/T]ATATGATAGAAGTCC | 10533 |
| rs112066480 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ATG7 | GRCh38.p7 | 3:11388692 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 10533 |
| rs112073311 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424594 | ATTAAATAATTTTAA[G/T]TTTAATAAATATTAA | 10533 |
| rs112106223 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ATG7 | GRCh38.p7 | 3:11382600 | AAGACCTTATTTGAC[A/G]TTTATATGAGTTGCT | 10533 |
| rs112110312 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ATG7 | GRCh38.p7 | 3:11353270 | AACATGGTGAAACCC[C/T]GTCTCTACTACTAAA | 10533 |
| rs112119212 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | ATG7 | GRCh38.p7 | 3:11417897 | CTCACTGAAAGCTCT[G/T]CCTTCTGGGTTCACG | 10533 |
| rs112119821 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511690 | CACAGGAGCCCATGG[A/C/T]GGGGGTGGGAGGCTC | 10533 |
| rs112156571 | in-del | -/T | 0.284209 | 0.247648 | intron-variant | ATG7 | GRCh38.p7 | 3:11554246 | GCTGTCTCCACTGTC[-/T]TTGCTCCAGGCCACC | 10533 |
| rs112172792 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | ATG7 | GRCh38.p7 | 3:11460886 | CTGATTCCATCCATG[G/T]GTATGGAGCCCAGAG | 10533 |
| rs112194529 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11347312 | TGAAGTCTATAAAAC[C/T]GTGAAAACTATTTCT | 10533 |
| rs112211671 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ATG7 | GRCh38.p7 | 3:11315652 | TCCTCTCCCACCCCT[A/G]CAGTTATCGAATCAG | 10533 |
| rs112234451 | in-del | -/G | 0.0314385 | 0.121371 | intron-variant | ATG7 | GRCh38.p7 | 3:11398059 | ACTGCACTCCAGCCT[-/G]GGGGACAGAGCAAGA | 10533 |
| rs112240421 | in-del | -/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11290506 | CCTGTTTTTACTTTT[-/G]GTAGTGGATCTTGGC | 10533 |
| rs112242353 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11369114 | TATTTGGCCTTTCTG[C/T]ACAGGCTGTGTCCCC | 10533 |
| rs112264525 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11351329 | CAGGTAGGCCTGACC[-/T]AGATGAGGGGTGGAC | 10533 |
| rs112269909 | snp | G/T | 0.108048 | 0.20579 | intron-variant | ATG7 | GRCh38.p7 | 3:11390088 | TGTTGTGTTGAAACC[G/T]CCTACGTATCCCAAA | 10533 |
| rs112285539 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11548936 | CGTGGCTGTTGCCAG[A/G]TTGTCCTCTGCAGGG | 10533 |
| rs112287206 | snp | A/T | 0.0174175 | 0.0916809 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271005 | TAATCTACTATCTGA[A/T]CAAGCCACCCCTTCA | 10533 |
| rs112289302 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11529676 | CTTCTTGATTTTTTT[C/G]TCATAATTGAGGCTT | 10533 |
| rs112296028 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11473857 | TACTGTGCTGTGCTC[A/G]GACTTCTGTTGAACC | 10533 |
| rs112304206 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11521897 | CTGACATGGAATGAC[C/T]CTAGACTGCCGCCGC | 10533 |
| rs112304374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530544 | CAATTCTTTCCAGTC[A/G]GCACCCATTCCAGAC | 10533 |
| rs112311808 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11389196 | CGAGATGGTGCCACT[A/G]TGCTCCAGCCTGGGG | 10533 |
| rs112314011 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11401345 | TCAATGTTGACATCT[G/T]CCAAGTATCCTTCAA | 10533 |
| rs112332243 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11541090 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10533 |
| rs112337127 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272632 | CTGTAGCCGCGTCCC[C/G]TCAGACTGGTTCAGT | 10533 |
| rs112339765 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11344808 | CAGGAGGTTGAGGCT[A/G]TAGTGAGCCAAGATC | 10533 |
| rs112357390 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11383663 | CTCCATTGGCCAGGC[C/T]GGTCTCTAACTGCTG | 10533 |
| rs112362739 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11372965 | TTTAGATAATTTTTT[A/T]AAAAATAGGAAAATG | 10533 |
| rs112367638 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11469815 | AACATGGTGAAATCC[C/T]ATCTCCACTAAAAAT | 10533 |
| rs112373350 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11283354 | CAAGAAAAACTACCA[A/G]CAGCTACCATTTATT | 10533 |
| rs112378581 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11417962 | ACAGGCACCCACCAC[C/T]ATTCTTGGCTGATTT | 10533 |
| rs112380085 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11515434 | TCAGCCACCTGAGTA[C/G]CTGGGATTACAGGCC | 10533 |
| rs112386078 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11537904 | TCCAAAATTGGGAGC[A/G]TCTTGCCCCAAGTCC | 10533 |
| rs112387796 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11550753 | TATGGTATGTTGTTA[C/T]GTTTTCTCTCAGTTT | 10533 |
| rs112389343 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11538912 | CCCTTAGTAATTCTT[C/G]AGAATGAGTGACTGA | 10533 |
| rs112390874 | snp | C/T | 0.180064 | 0.240019 | intron-variant | ATG7 | GRCh38.p7 | 3:11471840 | TGCCTCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10533 |
| rs112392669 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11374720 | ACCATCCTGGTTAAC[A/G]TGGTGAAACCCTGTC | 10533 |
| rs112409229 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11383911 | TATATGGTGAAATGT[A/T]TGAATCTTAAAACAA | 10533 |
| rs112421964 | in-del | -/AG | 0.0715223 | 0.175059 | intron-variant | ATG7 | GRCh38.p7 | 3:11276540 | TTGCTTCCTGTACTT[-/AG]CCCTAAGTCATTGCT | 10533 |
| rs112430290 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11328781 | ACAGTTCACAATACA[A/G]TAAGAGATATGAAAC | 10533 |
| rs112434397 | snp | C/T | 0.202035 | 0.245356 | intron-variant | ATG7 | GRCh38.p7 | 3:11546240 | GCAGTGGCGTAATCT[C/T]GGTTCACTGCAACCT | 10533 |
| rs112439494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11290028 | CCATGTGTTTTCTCA[C/T]ATCCTGGTAGCTGCA | 10533 |
| rs112460260 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487451 | CGGACGGGGCGGCTG[C/G]CCGGGCGGGGGGCTG | 10533 |
| rs112471488 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555985 | GTTCAGCTCATGGGA[A/G]CTTCATGGGGACACA | 10533 |
| rs112472642 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11476128 | CAGGTCCTCTCCTTT[A/G]TACCCTAAGGTGTAG | 10533 |
| rs112474379 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11478400 | ACACCCATTAATGGT[A/G]TGGTCTAAGGACAAG | 10533 |
| rs112481084 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | ATG7 | GRCh38.p7 | 3:11315788 | CTGGAGCGCAGTGGC[A/G]CAATCTTGGCTTACT | 10533 |
| rs112501139 | snp | A/G | 0.0154807 | 0.086838 | intron-variant | ATG7 | GRCh38.p7 | 3:11403218 | TAAATGTAAACTGAC[A/G]TGCACCTATCAATCT | 10533 |
| rs112514914 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11349186 | CTGATTGGTGCGTTT[C/T]TACAGAGTGCTGACT | 10533 |
| rs112514995 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11491200 | TTCTCTAAACTTCCC[A/T]TCTTGCTTCATTTCA | 10533 |
| rs112520830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532680 | GTGAGTCATGACTGT[A/G]CCACTGCACTCCAGT | 10533 |
| rs112528807 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11338369 | GTCATTGATGGGCAT[C/T]TAAGCAGATTCCATG | 10533 |
| rs112538334 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11461614 | TGTAGTTCTTAGAAT[A/G]AGAATTCTTAGTGGT | 10533 |
| rs112541214 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11453352 | ATCCAGAGCCATCTT[C/T]ATGAAAGATAATACT | 10533 |
| rs112559922 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345171 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 10533 |
| rs112561995 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11543338 | GCTGGGGTTGGAAAG[G/T]CTGGGAGAACTCCTC | 10533 |
| rs112564113 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11367759 | TGGGTTTGTTTTGGG[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs112571803 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11459853 | GGCCACGTATAGTAA[C/T]AGTAGATGATGCTTA | 10533 |
| rs112572010 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11317960 | TTCTTTGTATTAGTT[C/T]ATCTGTTAAATGGTG | 10533 |
| rs112575359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553594 | GAGCTCGGTGGGGAC[C/T]TGACCCAGAGATAGG | 10533 |
| rs112581649 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11444177 | TGCTATGTAGTGTTT[C/T]ATAATTGGATATATT | 10533 |
| rs112613224 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11323358 | TATCATAAATGTTTC[A/C]CCAAGACCCTGCCAG | 10533 |
| rs112648703 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11497763 | TTTAGTTTCCCATGT[C/G]TCTGCCAATATTCCC | 10533 |
| rs112652521 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11330868 | AGGGAGGAAATATAT[A/G]TTAGCAAAATCAAGA | 10533 |
| rs112652676 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11504848 | AACACTGGATGTAGA[G/T]CTAACCAAAATTATA | 10533 |
| rs112663613 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11334055 | CTCCCGGCCAGCTTC[A/G]GGAATATTTCTTACC | 10533 |
| rs112664437 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11380908 | GAATTCTAGGGATGT[A/T]TTTCTCTATTCTGAG | 10533 |
| rs112667475 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11349462 | GGATTGCTTGAGCCT[A/G]GGTGGTCAAGGCTGC | 10533 |
| rs112686479 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11384170 | TGACCAAAACCTTTT[C/T]TCAGACCTGCAGAGT | 10533 |
| rs112694104 | snp | A/G | 0.18989 | 0.242666 | intron-variant | ATG7 | GRCh38.p7 | 3:11484712 | CCTGACCCCACGACA[A/G]TCCCCAGAGTGTGAT | 10533 |
| rs112696639 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11502776 | CTATAGATGCATCTG[A/G]AAGTGTGAAGTATGG | 10533 |
| rs112706213 | in-del | -/G | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11431383 | CCAGCCTGCAAGGGC[-/G]GGGGGGAAAAAAACA | 10533 |
| rs112717174 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11380943 | CAAGCTTCCTTTGAA[A/C]ACTGTACTTGGGCTA | 10533 |
| rs112720751 | snp | A/G/T | 0.0412711 | 0.13875 | intron-variant | ATG7 | GRCh38.p7 | 3:11377217 | AGGGTTTCCTGTCTT[A/G/T]AATTATCTAAAACTG | 10533 |
| rs112727977 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11420154 | AGGATGTTTGGGGGG[A/G]AAAATCCTTGTACTT | 10533 |
| rs112730060 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11398741 | CCTGTAGTCCTAGCT[A/G]CTTGGAGGCTGAGAT | 10533 |
| rs112738779 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11399164 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACTCCATT | 10533 |
| rs112738965 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11453828 | AAGGGGTGGGGGGGA[C/T]ATCTGGAGCCTGAAG | 10533 |
| rs112743106 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11464355 | TCCAGCCTGGGTGAA[C/T]GAGCAAGACCCTGTC | 10533 |
| rs112743560 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11441500 | ACCCACCTCGGCCTC[C/T]GAAAGTGCTGGGATT | 10533 |
| rs112753313 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ATG7 | GRCh38.p7 | 3:11537491 | AGGTGTTCAAAGGAT[A/G]CTGGCTGAATGGATG | 10533 |
| rs112783399 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11379849 | GAACTTATTTTTGCT[A/C]ATAATCTCTTTCCGG | 10533 |
| rs112785350 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11372495 | TATATAGTAAAATGA[A/G]CCCATTTTAGTATGA | 10533 |
| rs112794448 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11405539 | ACATTGCTATGTGTC[A/G]TCTTGTCATGTATTT | 10533 |
| rs112817430 | snp | A/C | 0.0711525 | 0.174681 | intron-variant | ATG7 | GRCh38.p7 | 3:11338292 | AGACATGATCTCGTT[A/C]TTTTTTTATGGCTGC | 10533 |
| rs112831481 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11411063 | CATTCCAATCAGCAA[C/T]GTAGAAGTCTTTTTT | 10533 |
| rs112836854 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11334778 | GCCTGGCCGATATGG[C/T]GAAACCCCGTCTCTA | 10533 |
| rs112843625 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ATG7 | GRCh38.p7 | 3:11343221 | GGTGTGAGCCACCAC[A/G]CCTGGCCAAACATGT | 10533 |
| rs112853131 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11402662 | ACCCCAGCTCCAAAA[A/C]TATAAAATCACAGAA | 10533 |
| rs112861271 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | ATG7 | GRCh38.p7 | 3:11272968 | GAATCAATCCGGTAA[C/G]GTAAATATAGGTGTT | 10533 |
| rs112862176 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11382063 | CTAAAAATTACTTTT[-/A]AAAATTTATCCTTTG | 10533 |
| rs112864291 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11536073 | CTCATAACTGGCTAG[C/T]TGGGGCAAGGAGACC | 10533 |
| rs112866544 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11413427 | ATGATTGTGTGGCTT[-/C]CCCCCCCGCCCCACT | 10533 |
| rs112866861 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11518158 | AGAAAGACTAGTTGT[A/T]GAGAGAGGGAGCAGG | 10533 |
| rs112892030 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11347417 | TCTAAAATATCATAC[A/C]GTGGGAAATAATTTG | 10533 |
| rs112892798 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11399170 | CTGGCCAACATGGTG[A/C]AACTCCATTTCTACT | 10533 |
| rs112898224 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11380755 | AAGGCTCATGATTGC[C/T]GATAAGTAAAGATTT | 10533 |
| rs112899922 | snp | A/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11440675 | TTGGTCCCCATTTGC[A/T]TTTTTTTTTTTTTTT | 10533 |
| rs112910565 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11453271 | GGAAAGGCCTGTCCC[C/T]AAGCTTTAGTAACTT | 10533 |
| rs112918758 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11306200 | CAGGTGTGAGACATT[G/T]TGTCTGCAGACAACC | 10533 |
| rs112936814 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11532307 | ACATCATCTGCAAGG[A/G]ACAAACCGGAAGTGT | 10533 |
| rs112938924 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ATG7 | GRCh38.p7 | 3:11281518 | TGGCTCACGCCTATA[A/G]TCCCAGTACTTTGGG | 10533 |
| rs112942210 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ATG7 | GRCh38.p7 | 3:11445540 | TGGAGGATGGAGGGT[A/G]GGAGGAGGAAGAGGA | 10533 |
| rs112946358 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11458118 | TCAAAACAGCCCTCT[G/T]TTTTGCTACAACAAA | 10533 |
| rs112955666 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | ATG7 | GRCh38.p7 | 3:11344710 | CATCTCTACAAAAAA[A/T]ATATAAAAATTAGCC | 10533 |
| rs112957010 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11531442 | TGAGGTCCCACCACC[C/T]CCTGTGTGCCAGTCC | 10533 |
| rs112973172 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11443034 | TAGTGTGAAACAGTG[A/G]CAACTGCTTGATTAA | 10533 |
| rs112987987 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11381166 | CTTTGTCAGTAGTTA[C/G]CCATGAGCCCATTCT | 10533 |
| rs113015950 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | ATG7 | GRCh38.p7 | 3:11477647 | AGAACTCTTTCAGTT[G/T]TAAGTTGCAAATTTT | 10533 |
| rs113019949 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11428999 | GTGGAGCAGAAGGGA[A/G]CATGGTTTCATCCAC | 10533 |
| rs113026035 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11325470 | TGAGGTCCGGAGTTC[A/G]TGACCAGCCTGACCA | 10533 |
| rs113037500 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11295639 | ATGACCAGTCATTTT[A/C]TTTGATTCCTAGTGT | 10533 |
| rs113045953 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11382204 | GGGAAGTAGAATAAG[-/T]TTCTGCTGAATAGTG | 10533 |
| rs113056709 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | ATG7 | GRCh38.p7 | 3:11443914 | TCAAAAAATACTCTC[A/G]TTGCCCTTCACCCAT | 10533 |
| rs113065265 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11466939 | GTTTGAGATCAGCCT[A/G]ACTAACATGGTGAAA | 10533 |
| rs113070394 | snp | C/T | 0.5 | 0 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313331 | TACCACTTCTACTAT[C/T]GGTTTTGCTATCCTG | 10533 |
| rs113076529 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ATG7 | GRCh38.p7 | 3:11395743 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG | 10533 |
| rs113089366 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11373681 | TTTTTAACTTCTTTG[A/G]GAGTTGCGGCCTGGC | 10533 |
| rs113091412 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11322319 | AATGATTTAAGAATC[A/G]CAAATAGCTCACCAC | 10533 |
| rs113096318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11340509 | CCTCAAGTCTCTTTT[A/G]GAAAGAAGCAAACCA | 10533 |
| rs113100712 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11290723 | GAGTTTCACCCTTGT[A/C]GCCCAGGCTGGAGTG | 10533 |
| rs113124207 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11538044 | TCCCAGTGTGGGATT[C/T]CAGATGACCCCTGTT | 10533 |
| rs113124797 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11415371 | ACTAAACTTAAAAAA[C/T]ATTTTTCTGTCTTCA | 10533 |
| rs113127124 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11542569 | CCCGTGTACCTCTCA[C/T]CTGGGTCCCTGGAGA | 10533 |
| rs113132478 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11482955 | CCCTTGAGCCCCTTA[C/T]AGTCAGTACCCCTAA | 10533 |
| rs113141872 | snp | A/C | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11392579 | CCAGGCCCAGCAAAA[A/C]CCACACCCCAAGGCT | 10533 |
| rs113143364 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11377502 | ACCCCAACTGGATCT[A/G]CTTTCTCCCTGTCCC | 10533 |
| rs113148742 | snp | A/G | 0.104859 | 0.203554 | intron-variant | ATG7 | GRCh38.p7 | 3:11541180 | GCTGGGATTACAGGC[A/G]TGAGCCATCGCGCCC | 10533 |
| rs113148981 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11412727 | TCTGCAAAAAACACC[A/G]TTGGATTTGTATAGA | 10533 |
| rs113150997 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11540909 | TTTTAGCTTTTTTTG[C/G]GGGGGGGAGGGGGGG | 10533 |
| rs113152568 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | ATG7 | GRCh38.p7 | 3:11307253 | TGGCAGGAAGGTCAG[A/G]GAGAGGACATCCAGG | 10533 |
| rs113158159 | in-del | -/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11391959 | TCCATTGTACTTATT[-/G]GGGGGGGGGTAATTT | 10533 |
| rs113167023 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11511632 | GTCGATGGGACTGGG[C/T]GCCGTGAGCAGGGGG | 10533 |
| rs113168472 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ATG7 | GRCh38.p7 | 3:11506463 | CCTATGTGCTTATGC[A/G]TATCAGCACTTTGGG | 10533 |
| rs113170328 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11544593 | CACCCCAGCTGCTCC[C/T]GCCTGGGGATGCTCA | 10533 |
| rs113174575 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11413424 | CGAGATGATTGTGTG[G/T]CTTCCCCCCCGCCCC | 10533 |
| rs113198565 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11550948 | TCTCTAACGTTTGGA[C/T]TTTTATCCCATTTGG | 10533 |
| rs113198581 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555378 | GAGCCGAGCTGGGTA[C/T]GAGACTAAAGGGCCC | 10533 |
| rs113199499 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490230 | CCTTTACAATTATGT[A/C]ATGGCCTTGTCTCTT | 10533 |
| rs113211173 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11462989 | CTCCTGGGTTCAAGC[A/G]ATTCTTCCACCTCAG | 10533 |
| rs113236470 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | ATG7 | GRCh38.p7 | 3:11353422 | GCACTCCAGCCTGGC[A/G]ACAGAGTGAGACTCT | 10533 |
| rs113239135 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | ATG7 | GRCh38.p7 | 3:11372015 | AAACGACCTATTCTG[A/G]TGCTTTTTGCATGCT | 10533 |
| rs113241007 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11470854 | GTCTGAGGAAGGCAC[C/T]GGCATTTATTACTTT | 10533 |
| rs113241670 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11319259 | TCTTTAGCATGATTC[C/G]AGTTTCCCTTCGAGC | 10533 |
| rs113249509 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | ATG7 | GRCh38.p7 | 3:11387049 | TATCCAGTTCCCTGT[G/T]GCCAAGTACCAAGGC | 10533 |
| rs113255202 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11379331 | GTTCTGAATAAATTA[C/T]TTCAGTTATAGTTTG | 10533 |
| rs113257987 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11509660 | GCCACCCCTCCCCCA[A/G]TCTATCTCTAATTTT | 10533 |
| rs113259424 | in-del | -/TGTGTGTG | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11366972 | ATATATGGGAAAAGC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 10533 |
| rs113264764 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ATG7 | GRCh38.p7 | 3:11374991 | GAGGATCGCTTGAGC[C/T]CTGAGTCCAAGACCA | 10533 |
| rs113279015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11328791 | ATACAATAAGAGATA[C/T]GAAACAATATTTAGG | 10533 |
| rs113291800 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11378408 | TAAATTCGGGCTGGG[A/C/T]GCGGTGGCTCACGCC | 10533 |
| rs113303014 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11394398 | TCTTCTTAAACATCA[A/G]ATCACTATTATAAGG | 10533 |
| rs113308792 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11530364 | GAAGCACTCTGCATC[A/G]CCACCTTCTGCATTT | 10533 |
| rs113317193 | snp | A/T | 0.0733688 | 0.176922 | intron-variant | ATG7 | GRCh38.p7 | 3:11334236 | GCTTTTCAGAGCACT[A/T]TCACAACATTTATTA | 10533 |
| rs113337717 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11389118 | CCACACTTGTAATCC[C/T]AGCTACTTGGGAGGC | 10533 |
| rs113339927 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ATG7 | GRCh38.p7 | 3:11273060 | GATGTTGGAGAAGTA[C/G]AAGCCAAACCGTGTG | 10533 |
| rs113355365 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11372884 | CGGCCATGTTTTCCC[C/T]TTGTGGGGAGAGGGG | 10533 |
| rs113372221 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11391961 | CATTGTACTTATTGG[A/G]GGGGGGGTAATTTCA | 10533 |
| rs113378851 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11543626 | AGCACAAGGCTGGCC[A/G]CGGTGGCTCATGCCT | 10533 |
| rs113383904 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11333172 | TTTCTTTTCATATCG[C/T]CACAATGGCAGAAGA | 10533 |
| rs113388410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315148 | CACACCACCATGCCC[C/T]TGGAAAGTGTTATAT | 10533 |
| rs113399231 | snp | A/T | 0.120674 | 0.21395 | intron-variant | ATG7 | GRCh38.p7 | 3:11389456 | TTTTTTTTTTTTTTT[A/T]AACACAGAATAAGCT | 10533 |
| rs113400615 | snp | C/T | 0.207559 | 0.246371 | intron-variant | ATG7 | GRCh38.p7 | 3:11397971 | TGCCTGTAGTCCCAG[C/T]TACTTGGGAGGCTAA | 10533 |
| rs113409574 | snp | A/C | 0.158302 | 0.232576 | intron-variant | ATG7 | GRCh38.p7 | 3:11337492 | TCTCTCTCTCTCTAT[A/C]TATATATATATAATT | 10533 |
| rs113427304 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11429148 | CGGCTTGCAGGTATG[C/T]ATTTTTTGGCCTGCC | 10533 |
| rs113431729 | snp | C/T | 0.0648419 | 0.167978 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287815 | CTCACTGATCTTTAC[C/T]GCCCTTTAAAAAGAT | 10533 |
| rs113465598 | snp | C/G/T | 0.0138938 | 0.0823076 | intron-variant | ATG7 | GRCh38.p7 | 3:11535723 | CGGGGGCGTGCGCTG[C/G/T]GGGGAGAACCTTGTG | 10533 |
| rs113468104 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487596 | GGGCGGGGGGCTGAC[A/C]CCCCCACCTCCCTCC | 10533 |
| rs113496991 | in-del | -/A | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11368890 | TTCTAAAGTACTGAT[-/A]AAAAAAAGACCCTGA | 10533 |
| rs113505182 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11516471 | GTGAGAATGTGGAGC[A/G]ACAGAAACTCTCATT | 10533 |
| rs113510975 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11329843 | ACATTTCCGATTTCA[C/G]CAGTTTTTTCCTGCA | 10533 |
| rs113518127 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11275510 | CCCACCACCATGCCC[A/G]GCTAATTTTTTTTTT | 10533 |
| rs113524180 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11469924 | GAACCTGGGAGGCGG[A/G]GGTTGCAGTGAGTGA | 10533 |
| rs113537871 | snp | C/T | 0.109108 | 0.206518 | intron-variant | ATG7 | GRCh38.p7 | 3:11431293 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10533 |
| rs113549834 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11379788 | TAAAGGACCTAATAT[A/G]GTTCTTCTGCAAACT | 10533 |
| rs113553411 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11483486 | GGGTAGGGAATACAT[C/T]TGAAGAGGAGTAACC | 10533 |
| rs113561671 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | ATG7 | GRCh38.p7 | 3:11514953 | TCAAGTGATTCTCCT[C/G]CCTCAGCTTCCTGAG | 10533 |
| rs113569874 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11423471 | TGCCACAACTTTCAA[A/T]TTTTTTTTCTTTTGT | 10533 |
| rs113571258 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11349200 | TCTACAGAGTGCTGA[C/G]TGGTGCATTTACAAT | 10533 |
| rs113574346 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11541720 | TCCTCCTCCTCTTCT[C/T]CCTCTCTCTGATGTT | 10533 |
| rs113585998 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11320290 | GTGCATCCCTTCTTC[-/T]TTTTTTTTTTTTGAG | 10533 |
| rs113586366 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11431546 | ACCTATTAAAAGGTC[A/T]CTCCCTGTTCCCTCC | 10533 |
| rs113598302 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11308918 | TTTCAGCTCCACACT[C/T]CACCTGAGAGTGAGA | 10533 |
| rs113618394 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11358218 | TGCCCTGCCTCAGGG[C/T]CCTGGGGTGATAGGT | 10533 |
| rs113632730 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11333265 | GCATGCTCTGCTATT[C/T]AGACTGGAACAAAGG | 10533 |
| rs113638271 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11275509 | GCCCACCACCATGCC[C/T]GGCTAATTTTTTTTT | 10533 |
| rs113638855 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11444778 | ATCAGTAAATAGATA[A/G]TCTACAGAATGGGAG | 10533 |
| rs113664058 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ATG7 | GRCh38.p7 | 3:11541152 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10533 |
| rs113670295 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513446 | CAGTGGGCCAGCACT[C/G]CTGGGGGACCCAGCG | 10533 |
| rs113673746 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11408305 | AGACCACCTTAGCCT[A/G]GACCTTGTTTATATC | 10533 |
| rs113677866 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ATG7 | GRCh38.p7 | 3:11305986 | ACTAATGAAATGAAT[A/G]TTTTCATTTAACATC | 10533 |
| rs113697353 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11481371 | GTTCTTACACTTTTT[G/T]AAAGTCAAGGTGAAC | 10533 |
| rs113698882 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11529528 | CCTTGGGCTGGTAGT[C/T]AGATGAGGTCAAGGG | 10533 |
| rs113700120 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11534066 | GTACTAGCCAGCAGA[A/G]AGCCTCCTCCTCCCC | 10533 |
| rs113702829 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11363145 | ATCTTTCCGGACAAA[A/G]TCACTATGGTTTATT | 10533 |
| rs113714463 | snp | A/G | 0.108048 | 0.20579 | intron-variant | ATG7 | GRCh38.p7 | 3:11513196 | CACCCAGTGGATCCC[A/G]CACCGGGGCTGCAGG | 10533 |
| rs113730102 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11462031 | GTGAGACTCTGTCTC[A/C]AAAAAAAAAGAAAGA | 10533 |
| rs113730970 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450911 | AGGGCTGGTGTCCTC[C/T]AGGGTGTATTAGTTG | 10533 |
| rs113731331 | snp | A/G/T | 0.0150843 | 0.0857313 | intron-variant | ATG7 | GRCh38.p7 | 3:11492156 | CAGGTGTGGAATACA[A/G/T]TCTCCTGGTGCGCCG | 10533 |
| rs113733332 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11404046 | CTACAATAGTATAAT[C/T]TCAAATATTGGATTA | 10533 |
| rs113753149 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11375039 | AGACCTCATCTCTCT[A/T]AAAAAAAAAAAAAAA | 10533 |
| rs113763506 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11378090 | TGGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 10533 |
| rs113765591 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11414469 | TATTTGGATTTTCTA[C/T]GTGGGCAGGCATGTC | 10533 |
| rs113774753 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11289234 | TTACTTTTTCAGGAA[A/G]TAGGTAATGTTTGGA | 10533 |
| rs113782018 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11438733 | GTGCATTTGCTGGGT[A/G]GGAGAGGTTTTTCAA | 10533 |
| rs113786112 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ATG7 | GRCh38.p7 | 3:11452581 | GTCCTCTAGGCACTT[C/T]AGCAAACAGCGTGGT | 10533 |
| rs113789883 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11335680 | CTATGATAAGGCTCA[G/T]GCTTGATGATGCTGA | 10533 |
| rs113803535 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | ATG7 | GRCh38.p7 | 3:11421281 | TGTAGCATGCAGTGC[C/T]GTTTGATAGCATTTT | 10533 |
| rs113817405 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ATG7 | GRCh38.p7 | 3:11406966 | ATTTCGTATCTTCAC[A/G]TTTCAAAACCAATCA | 10533 |
| rs113835936 | snp | C/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11417906 | AGCTCTGCCTTCTGG[C/G]TTCACGCCATTCTGC | 10533 |
| rs113838038 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ATG7 | GRCh38.p7 | 3:11459261 | TCTCTGCAGAATGCT[A/G]CATGAGATTTGCCCT | 10533 |
| rs113870778 | in-del | -/A | 0.0460142 | 0.144533 | intron-variant | ATG7 | GRCh38.p7 | 3:11419563 | TGTCTCAAAACAAAC[-/A]AAAAAAAAACACACT | 10533 |
| rs113893243 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11537257 | ACTGAGAGGCCTTAC[C/T]CCCAAGTCCCTTTCT | 10533 |
| rs113902569 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ATG7 | GRCh38.p7 | 3:11368575 | GGTGGGAGAATTGCT[C/T]GAGCCCAGGGGTTCA | 10533 |
| rs113918817 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487611 | CCCCCCACCTCCCTC[C/T]CGGACGGCACGGCTG | 10533 |
| rs113923893 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11370856 | TGTTCGGGAGTTTTG[-/T]TTTTTTTTTAATTCC | 10533 |
| rs113942485 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11349153 | TGCATTTACAATCCT[C/T]TAGCTAGACACACAG | 10533 |
| rs113957105 | snp | A/G | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11554558 | GGACATGCAGGAGGT[A/G]AGCAGAGGCACATTC | 10533 |
| rs113958368 | snp | G/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11553163 | CCCTTCCTCCAGGCA[G/T]CCCGCCCCGCCCTTT | 10533 |
| rs113961637 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11519358 | ACTGTGTTTCCTTGA[C/T]GCAGTATTTCTGGAT | 10533 |
| rs113963240 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11535356 | ACTCATCTCTGTCTC[C/T]CAGTGGCACCCAGCA | 10533 |
| rs113974008 | snp | C/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11405816 | GTAGAGATGGGGTTT[C/T]GCTGTGTTTCCCAGG | 10533 |
| rs113978429 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11474747 | CTTCTGAGCTGAGCC[C/T]GGAATGCAAAGAAAG | 10533 |
| rs113985438 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352375 | TATACCCAGTAATGG[A/C/G]ATGGTTGGGTCAAAT | 10533 |
| rs114030559 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ATG7 | GRCh38.p7 | 3:11549260 | GTTTTCTTAAAAACT[A/G]TATATATTCAAAGTG | 10533 |
| rs114055886 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ATG7 | GRCh38.p7 | 3:11553344 | TTCGCAGCAGGTCTA[C/T]ACAGCGTGTGGCACA | 10533 |
| rs114094834 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11359378 | AATTAGAACTATGAA[A/T]AGTTGTTATAGTATA | 10533 |
| rs114102892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353923 | AGTGTACCAGGAGGT[C/T]ATGAGCACCCTTTAC | 10533 |
| rs114110405 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11503480 | AAAGGATATTCAGGC[C/T]GGGCGCAGTGGCTCA | 10533 |
| rs114141670 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11378375 | TGCAATCCGAGATCA[A/G]GTGTTTGATAGAAAT | 10533 |
| rs114150201 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11495529 | GGTGCCCAGACCAAG[C/T]CACTGACTAGTTGTG | 10533 |
| rs114156307 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11493422 | AGGCAACATTCAATT[G/T]GTAAAAAGACATTAT | 10533 |
| rs114200578 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557127 | ACACAGCACACCCCA[G/T]GGGGAGGGGATAGAA | 10533 |
| rs114209470 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11521038 | CAGAGTGGACAGCTG[C/T]AGACCATTGGGTTCC | 10533 |
| rs114213497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382311 | AGTGCGAGCACGCAC[A/G]CACGCGAGCGAGAGC | 10533 |
| rs114213895 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11295535 | GATTCTGCCTTTTAT[A/T]GCCTGTTCTCTTTTA | 10533 |
| rs114214294 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11483188 | GCATTCTCCCCGTCC[C/T]CCTGCCCCTAACCCA | 10533 |
| rs114293525 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11539821 | ACCAGCACAGTTCGG[C/T]GACATCGAGCAGGTC | 10533 |
| rs114294839 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11498734 | TCTAATTGCTCTTTC[C/T]CCTTTCTGTAGGTCA | 10533 |
| rs114298794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11549408 | CAGTGTACAGTCCAG[C/T]ATGATTAACAGTAGT | 10533 |
| rs114319497 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | ATG7 | GRCh38.p7 | 3:11398614 | TCTCAGCACTTTGGG[G/T]GGTCAAGGCAGGAGG | 10533 |
| rs114320717 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ATG7 | GRCh38.p7 | 3:11299698 | CTCTTGATTTTGATT[A/G]TAGTTAATATTTTGT | 10533 |
| rs114322128 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11394419 | TATTATAAGGAGATT[A/C/G]TGAGTTGAGCTTTGA | 10533 |
| rs114327328 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272199 | CCGACATCTGGTAAG[A/G]GAGACGCTCTCCATC | 10533 |
| rs114330130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283949 | AGAAAAACAAACCAA[A/C]AAAACTCCCCTGCTC | 10533 |
| rs114344228 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11463748 | GTGTGACTACTGGCA[A/G]CTCCAGAGCCTCATA | 10533 |
| rs114350639 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11409727 | GGTAGGTCTGTGATA[C/T]ATTTTGAGTTATTTT | 10533 |
| rs114350997 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11380816 | GGTGACCACTAATCC[C/G]CAACTGTGGCTTCTC | 10533 |
| rs114357214 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11358982 | ATGGTGCATACCTAT[A/G]ATGGAATAGTATGCA | 10533 |
| rs114359744 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | ATG7 | GRCh38.p7 | 3:11516022 | TTGGGAACAGCTCAC[A/G]TTCCTTTTTAAAAAA | 10533 |
| rs114360804 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11328772 | GCATAGAAGACAGTT[C/G]ACAATACAATAAGAG | 10533 |
| rs114393740 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11420432 | ATCTGTGGAAACATA[C/T]AATCTGAATGTTTAA | 10533 |
| rs114402220 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11348155 | TTTCTACCAGCCACT[C/T]GCTATGTGGCTGAAC | 10533 |
| rs114402641 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11455757 | CAGTTATGGATCCCA[C/T]CTTAATCAAGCTGAT | 10533 |
| rs114406162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11300291 | CTGTTCTTTGAGACT[C/T]GCCAGGTGTGATTTT | 10533 |
| rs114418035 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11303150 | CAGCCAAGGTGCAAA[A/C]AGGTGGAAGAGACAC | 10533 |
| rs114427333 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11475583 | CTTAGATAAAACAGA[C/T]GCGGATGCTACCCTC | 10533 |
| rs114436593 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11383489 | TTCTGACTACCTTCT[C/T]CAACAGTGAGAAACC | 10533 |
| rs114440748 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ATG7 | GRCh38.p7 | 3:11424703 | AAAGTTAAAGTAGTA[C/T]AAAATAATCTACAGA | 10533 |
| rs114470929 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11506059 | GAACATTTCTGTATA[A/C]ATCTTGCTTTCAGTT | 10533 |
| rs114471034 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11276991 | CCTCTCCTTTCATTT[A/C/G]GTCATCCAAAACAGA | 10533 |
| rs114475518 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11308107 | TCGGCTTACCGGAAA[C/G]TGGGGGCCTCTCTTC | 10533 |
| rs114479980 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | ATG7 | GRCh38.p7 | 3:11551493 | GGAGAGATTCTTCTA[C/G]GACTGTCGCAGCTGT | 10533 |
| rs114510538 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11286042 | TAGAATGTTTTTCAA[C/T]TTGGGTTTATCTGAT | 10533 |
| rs114516853 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11548805 | GGCCTGTTCCCAGTC[C/T]TTTCCTGTAAGAGAT | 10533 |
| rs114521567 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11528038 | CTTGAAGATCACCCA[C/T]GTGTGGTCCCTTCTG | 10533 |
| rs114533237 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11394528 | AAGGAAGTTGAGAGC[A/G]TGAGCCACACCTTTA | 10533 |
| rs114541468 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11431986 | CAGGTACCTGGAAAT[G/T]ATTGCAATGATTTTG | 10533 |
| rs114545099 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11279916 | CTTCAAAATTGTTAG[C/T]TCTTTAAAGGTGGGG | 10533 |
| rs114555962 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11500976 | TGAAAATAATAGGGC[C/T]GGGCATGGTAGCTCA | 10533 |
| rs114593225 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11495890 | GCAAGATGCAAAATA[G/T]ATATAATGGATGTTA | 10533 |
| rs114602915 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11544068 | CACTCCTTCAGGCTG[C/G]TCATCTGCCCGCACC | 10533 |
| rs114614306 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11418987 | CCCGATCCAGTCACC[A/G]CCCACCAGGTCCCTC | 10533 |
| rs114620463 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ATG7 | GRCh38.p7 | 3:11524873 | TCATCCTCCAGGTGA[A/G]GTTCTGTGTCTTACA | 10533 |
| rs114631124 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | ATG7 | GRCh38.p7 | 3:11370315 | TCATGTCCAGCTTAG[A/T]TTTTCTGCCCCCTTG | 10533 |
| rs114644357 | snp | G/T | 0.039522 | 0.134904 | intron-variant | ATG7 | GRCh38.p7 | 3:11550579 | TTTTAAAAAATTATT[G/T]TAGAGAAAGGGTCTC | 10533 |
| rs114676404 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ATG7 | GRCh38.p7 | 3:11460491 | AGGGTAGCACCAGAG[C/T]GTTGCCTTTGCCAGC | 10533 |
| rs114677455 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11491769 | CTGGGTACTAGCAGC[A/G]GTGTCTGCAGAATAG | 10533 |
| rs114732076 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11536409 | CTCCACCTGGCCAGC[A/G]CCCTGTTCCCACAGC | 10533 |
| rs114746872 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11483150 | TCCCTTTTCTGCTCT[A/C]CTTGCCCCTCACATT | 10533 |
| rs114751681 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11388068 | GCTCTATGAGTGTTT[C/T]TTTGGTACCATTCCC | 10533 |
| rs114755647 | snp | C/T | 0.030278 | 0.119257 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556595 | TTACAGACAAATCTA[C/T]GACAAAAAAAAAGAT | 10533 |
| rs114756390 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11329656 | TAAAATAAACTTTTT[A/G]TTTTGGGATAATTTT | 10533 |
| rs114798639 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11476614 | ACAAGGTAGATGGAA[C/T]GGTAACTCACTTTAT | 10533 |
| rs114819702 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11534821 | TGCACAGCACCCCTT[C/G]TACCCTAGGGAGGAG | 10533 |
| rs114820735 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11537552 | TCCTGATTTCTTAGT[C/T]TCAGTTCCCATTTTC | 10533 |
| rs114823205 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ATG7 | GRCh38.p7 | 3:11502086 | TGTAAAATAACAGTA[A/G]CATATGTCATTTATG | 10533 |
| rs114843674 | snp | C/T | 0.0329836 | 0.124112 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555333 | GTGAGCGCACTGCAC[C/T]CTGGCCCTGGTGGAG | 10533 |
| rs114851724 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11331046 | CCTCCTTCATTCCCC[A/G]TCTTCCTTCCAGTCT | 10533 |
| rs114864159 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11479839 | CTTCTCCACTTAGGG[C/G]TGTGTACCATTACTA | 10533 |
| rs114864966 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11453500 | AGCTAGAAAAGGGTG[A/G]AGAAGTAGGCGGGAG | 10533 |
| rs114881311 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11401015 | TGTGCTGCTTAATGG[A/G]TTGAATCCCAAGATG | 10533 |
| rs114914279 | snp | C/T | 0.0142815 | 0.0833581 | intron-variant | ATG7 | GRCh38.p7 | 3:11503157 | CAAAAGAGCAGTTGT[C/T]GGGGGCTCTTTGAAT | 10533 |
| rs114920782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405197 | ATGAGGACATTTTGT[C/T]AGTGGATCTTCCTGA | 10533 |
| rs114926483 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11428228 | TAGGTTGCATATCCT[A/C]ACCATTCAGGGAGGC | 10533 |
| rs114931756 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11338703 | GGCATTAAAAAATAC[C/T]ACATCAGAGTGCCCG | 10533 |
| rs114933088 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471745 | TGGCTTTTTAGATTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs114946926 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11509868 | AATCAGGCAGCCAGC[A/G]CTCCATACTTATTTA | 10533 |
| rs114994899 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11308347 | CTCAGTACTTGCTGA[A/G]TATACATAAATTTGA | 10533 |
| rs114997084 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11523291 | GGGGAAATAGGGAAC[G/T]TTCAATTGTGTTTTA | 10533 |
| rs114999573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11300464 | TACAGGGATTTTGCT[A/G]TCTTCTACAGAAATA | 10533 |
| rs115018307 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | ATG7 | GRCh38.p7 | 3:11334044 | ATGAGCCACCGCTCC[C/T]GGCCAGCTTCGGGAA | 10533 |
| rs115019752 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11307573 | GACCTCTTTACTCTT[A/G]CCCTTGCATTCTCTG | 10533 |
| rs115027033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11540807 | AATTTTTTTCTCTTA[C/T]AGTTCCTGCTTTTAG | 10533 |
| rs115046175 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11461528 | AGGAAATTGAGTTCA[C/T]GGTCTAAGATCACAG | 10533 |
| rs115052983 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11328469 | TATTAAATTAAATAC[A/G]AATCTGTCTATTTGC | 10533 |
| rs115139766 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11403972 | GTTTGCATTTTTCCA[A/G]TTTACCTCCTTGTTG | 10533 |
| rs115189398 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ATG7 | GRCh38.p7 | 3:11522975 | TCAGCCCTGTTTTCT[C/T]ATCTGTAAAATGGAC | 10533 |
| rs115215954 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11359573 | TGGTGATGCACACCC[A/G]TGCTCCCAGCTACTC | 10533 |
| rs115225498 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ATG7 | GRCh38.p7 | 3:11276601 | AAGTCATCAGACCTC[A/G]ACATTGCCAGAATAC | 10533 |
| rs115263088 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11456474 | GTTGTATGAAGTACA[C/T]GTTTTTGTTGTTTTG | 10533 |
| rs115264586 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11481134 | CAAGCATGTGCTTTG[G/T]GCAGAGCACTGTGTA | 10533 |
| rs115266460 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11459027 | CATTCATCACCCCCC[C/G]ATCTATGGAAAAATT | 10533 |
| rs115277572 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11494246 | CATGCAGGAAAACAG[A/G]AATTAGGGAGGGGTA | 10533 |
| rs115302303 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11514027 | ACTCATGTGCCACTA[C/T]GCCAAGCTAATTTTT | 10533 |
| rs115314502 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ATG7 | GRCh38.p7 | 3:11447910 | AACAAACTGATGCAG[A/T]TGGATGGGTGTTGGG | 10533 |
| rs115329879 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11441200 | CCATACTTAATTTTA[C/T]CCAATGCTTTATTAA | 10533 |
| rs115345324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323007 | TGAAGGCTGAGGCAG[G/T]AAGATTCCTTGAGCC | 10533 |
| rs115346046 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11278461 | CCTCCGTTCAGGGTC[C/T]GTGACTTCCCGCAAC | 10533 |
| rs115384777 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11317528 | ATTTTCTGTTTGAGA[C/T]TCAAAGTCACACGAC | 10533 |
| rs115390718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550399 | GGTCTTTCTCTTCTT[G/T]AATTTTATTTATTTC | 10533 |
| rs115393345 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379349 | CAGTTATAGTTTGTG[A/C]AACCTGATTATAGCT | 10533 |
| rs115399413 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11337056 | GCACCTGGTGGAGGA[A/G]GATGGCAGACACTGC | 10533 |
| rs115405232 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11300202 | AAAGTGCTGCTGGGA[A/T]TACACGATCGAGCCA | 10533 |
| rs115405283 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | ATG7 | GRCh38.p7 | 3:11325175 | TAAGAACACTCTGTG[A/T]TGTTGGTATGACGGT | 10533 |
| rs115436270 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | ATG7 | GRCh38.p7 | 3:11415698 | GGTCTTCAGGGGCAA[A/T]AACATGCATAGAGCT | 10533 |
| rs115439067 | snp | A/C | 0.0228947 | 0.104514 | intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11477238 | CTTTTATTCCTCGCC[A/C]ATCTGATTCTTGGCT | 10533 |
| rs115441593 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11364098 | CAGGTCCTGTGTCAC[A/C]TCTTTTTGGTGCCAC | 10533 |
| rs115453251 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11390926 | TGCTACCCACTAACC[A/G]TGTGACCTTGAGCAA | 10533 |
| rs115454488 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11285548 | CTTGTGGCTTTTTAC[A/G]TAGGTATATGCCTTG | 10533 |
| rs115457682 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11312989 | TAAATACCTCCCAGG[A/G]GGGTTTTGTAGGTTA | 10533 |
| rs115462573 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11390955 | AAGTATCTCAAACTT[A/T]GAGCTTCAGTTTCCT | 10533 |
| rs115478422 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11493812 | ACAATCTGGGGCATC[A/T]CAAAGAGATTCGGTA | 10533 |
| rs115498687 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11427343 | TGTTCTTCAGAAAGA[A/G]CATGCCTGGCTTTTT | 10533 |
| rs115501366 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495493 | CCAGCAACTCCCTGC[A/G]CTGTTGGTCAATAGA | 10533 |
| rs115513702 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11306820 | TCCAAGAAAACATAC[A/G]GTTAATCTTCTGTTT | 10533 |
| rs115524897 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11472142 | CAAACATGAGAATGT[A/G]TTTGTTCTTAAACCT | 10533 |
| rs115527515 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11525498 | TGTATGTGACAGATG[C/T]TCATTTGTTTGTTGA | 10533 |
| rs115563323 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11329792 | TGTCAAAACTAAGAA[A/G]CCAGAATTCTTACAT | 10533 |
| rs115565375 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11420627 | AATATTGCAGTAAAT[C/G]AAGTCTCACAATTCC | 10533 |
| rs115584454 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11339017 | AAACCAGTGTACAGG[A/C]CGGGCGTGGTAACTC | 10533 |
| rs115640694 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11456822 | CGCGTTCACACTGTA[C/T]GTGTACCCTTTTCTG | 10533 |
| rs115642520 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11403439 | TCATCTTGTTTGTGT[A/T]CAGAGAAAATCTGGA | 10533 |
| rs115644551 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ATG7 | GRCh38.p7 | 3:11524949 | ACAGAAACAAACCTC[A/G]TATATTCTATATTTT | 10533 |
| rs115698977 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11529103 | ACAGTGGAAACTACA[C/T]GTGTAGGTGGACAGG | 10533 |
| rs115714164 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11293047 | GGTGATACTATTAAG[A/C]AAACTAGGAAATACA | 10533 |
| rs115717016 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ATG7 | GRCh38.p7 | 3:11512561 | GAAGCCATGGACCGT[C/T]GCAGTGAGTGTTAAC | 10533 |
| rs115721039 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | ATG7 | GRCh38.p7 | 3:11341069 | ACTCCCCCGCCCCGT[C/G]CCCCACCCCGCCCCA | 10533 |
| rs115721700 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11275802 | GCAGACTGAGGAATA[A/G]CCTATTCACTCCATC | 10533 |
| rs115752398 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11373549 | CAAGTTCCAGGGGCT[C/G/T]CTTCTGATGAGGCAA | 10533 |
| rs115755167 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11429633 | TAGATAATGCACTTG[A/T]TATAAAATTTAAAGG | 10533 |
| rs115757856 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11498666 | GCCAGGTGTCCTCAC[G/T]GACTCCAGAAGAGGC | 10533 |
| rs115811806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11305873 | TTACATGGACTTTAA[A/G]TGAAAAGACATAGGT | 10533 |
| rs115823716 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11373063 | TTACAGAAAGAGTTA[A/G]CTTTTTTTTTGAAAA | 10533 |
| rs115825783 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11282454 | GTGAGGAGGACAACT[C/G]ACCCATCATAGCAAT | 10533 |
| rs115828656 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ATG7 | GRCh38.p7 | 3:11503268 | CAGAAACCAAGTATT[C/T]CCAGATGTCTAACTC | 10533 |
| rs115836875 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11390636 | CTCATAATAGCCTCA[A/G]CAGTGGTAACTTTTT | 10533 |
| rs115870267 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11418941 | TGAGAACTCGCTATC[A/C/G]CAAGAACAGCATGGG | 10533 |
| rs115885624 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11437475 | GGGAAGATGAGAGCA[C/T]GTTGCTATCTGTTTG | 10533 |
| rs115900171 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11430341 | AAAATATATATATAC[A/C]TTTACGTATATCTGT | 10533 |
| rs115973077 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11520744 | TCTGGGCCTTGGCTT[A/G]TCAGTAACTGGCAAT | 10533 |
| rs115978358 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11414454 | AACAGTGTTTTTATT[C/T]ATTTGGATTTTCTAC | 10533 |
| rs115983800 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11454651 | TTTAGCTTGAGTAAA[C/T]AAAGGTTGAGATTTC | 10533 |
| rs115985834 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11524654 | TAGTCGAGAATGGTA[A/G]TGCATATCTGTAGTC | 10533 |
| rs115986304 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11296548 | CAAAGCCCTTTACCC[A/C]CTGCGGAATCATATT | 10533 |
| rs115997969 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ATG7 | GRCh38.p7 | 3:11278468 | TCAGGGTCCGTGACT[C/T]CCCGCAACAGAACTC | 10533 |
| rs116008561 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11358336 | GAACACAAGTAAGTG[A/C]AGGCAGCTGTGGGAA | 10533 |
| rs116051364 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11541764 | CTTTGAGGTAGAGAA[C/T]AAACATGTAAAAGTG | 10533 |
| rs116053115 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11388067 | TGCTCTATGAGTGTT[G/T]CTTTGGTACCATTCC | 10533 |
| rs116054333 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11285850 | ATCCATCTCCCAGAG[A/T]CTCCCATTCAGTTTT | 10533 |
| rs116059077 | snp | A/C/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11537408 | CTCCCAGGGCAGGGA[A/C/T]GGACGCACCTGTCCC | 10533 |
| rs116080632 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11272350 | CGCGCCGCTTCCCAG[A/T]GGCAAGCGCGGGCAG | 10533 |
| rs116082196 | snp | G/T | 0.040671 | 0.13668 | intron-variant | ATG7 | GRCh38.p7 | 3:11552320 | TATACTTCTCTTGTG[G/T]CAGTGTTTTGCCATA | 10533 |
| rs116092264 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11523102 | GTAGGAAATGCTTCC[G/T]TGGGTGTTTGTATTA | 10533 |
| rs116096307 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ATG7 | GRCh38.p7 | 3:11513529 | GCAGGGCCAGCCGGC[C/T]GCTCCCAGTGCGGGG | 10533 |
| rs116096788 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557670 | TCTGAAAAGAAGATA[A/G]TAAGTATTAAGGTTT | 10533 |
| rs116110082 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11278460 | CCCTCCGTTCAGGGT[A/C]CGTGACTTCCCGCAA | 10533 |
| rs116113289 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11299642 | CAGAGTCAATTAGGT[A/G]CCAGGTGCCATCTAG | 10533 |
| rs116114781 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11391221 | CAAGATGTGAGCAAA[C/T]ACTAATGTGCAAGTT | 10533 |
| rs116124183 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11517481 | AAAAGAAAAAAAACT[C/T]GATCCCTGTCCTTAC | 10533 |
| rs116127205 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11414878 | TTCAAATGTTGAACC[A/T]GGCTTGTGCACCTGG | 10533 |
| rs116128610 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11463487 | GATATTTCTTATGGC[C/T]TCCCATCCCAATTCA | 10533 |
| rs116140942 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451194 | AAGAACTTGATAAAA[C/T]AGAAGTAAAGGTTGA | 10533 |
| rs116156667 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297487 | GGAGCTGCCAGATTT[A/C]TTTAGTATTGTCCTT | 10533 |
| rs116166360 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11528552 | TTAAAATAGTTTGGG[C/T]GCAGTGACTCATTCC | 10533 |
| rs116174753 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11408451 | CAGTTCCATATTTGC[G/T]TCCACATTTTGGGTA | 10533 |
| rs116196294 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11480740 | TCTCAGTGAATTTCC[A/G]TAACAATTCACTGCC | 10533 |
| rs116196480 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ATG7 | GRCh38.p7 | 3:11529203 | CCTCCAAAGCCAGCC[A/G]GGTTGAAGAGTTGGG | 10533 |
| rs116213945 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11437088 | CAGATGTTTAAAAAG[C/T]AAGACAAAAAGTGCC | 10533 |
| rs116235353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458103 | ACTAGTGTCTTGTTT[C/T]CAAAACAGCCCTCTG | 10533 |
| rs116303190 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11330479 | TTACAGTTGGTGCCT[A/G]TATCACCTTGGCATG | 10533 |
| rs116309920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11390952 | AGCAAGTATCTCAAA[C/G]TTTGAGCTTCAGTTT | 10533 |
| rs116316383 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11403252 | GAAGTCTTGACAAGA[C/G]TCTTTTGGAGTGCGG | 10533 |
| rs116350816 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11521072 | TTTCCCCTTCCATGA[A/T]ATGGGGAACATGGTA | 10533 |
| rs116359432 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11319533 | ATCTCATTGTGCCTA[C/T]AACTCCAGAAACCAT | 10533 |
| rs116373201 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11329780 | CCACGGTTCATTTGT[C/G]AAAACTAAGAAGCCA | 10533 |
| rs116382199 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11396641 | CTAAAGTTTAGCCGG[G/T]CATGGTGGCAGACAC | 10533 |
| rs116383262 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11442715 | GAAGACCAGCTTGGG[C/T]AGCATAGTGAGACTC | 10533 |
| rs116383940 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11482695 | TCTGAGTGATAGAGA[C/G]CTGACCTCTTCCATA | 10533 |
| rs116401093 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11416393 | TATTTTATAGAAATA[A/G]GCCTGTTTAGAATTT | 10533 |
| rs116405488 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11553803 | CTTCTATTTATTTTC[A/G]ACATCCTCGACTTTG | 10533 |
| rs116414253 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11316834 | AAGTTCTGAAATCAA[A/G]TGGAATCATCTCCAT | 10533 |
| rs116428120 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ATG7 | GRCh38.p7 | 3:11319746 | TCTGGTTATCCTACC[A/G]GACAGCTGTCTTCCC | 10533 |
| rs116487031 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | ATG7 | GRCh38.p7 | 3:11370329 | GTTTTTCTGCCCCCT[G/T]GGTGACTCTAGCTTA | 10533 |
| rs116488218 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11311990 | ACAGAGACAGAAAAT[A/C]GATTAGTGGTTGCCA | 10533 |
| rs116490305 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11468400 | TGCCTCGCCTATCCT[C/T]CTCCCCACTCCATGT | 10533 |
| rs116493398 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11376194 | TCTGAGAGAGGGGAG[A/G]ATGAGGACTAATTGC | 10533 |
| rs116510612 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11476367 | ATGCCGTGGATGCGT[C/G]AACAATGGCTGGTAG | 10533 |
| rs116512463 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11324816 | ATAAAGCCTAGACCC[C/T]GAGAATATTTGATAG | 10533 |
| rs116528484 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ATG7 | GRCh38.p7 | 3:11279345 | GTTGAGAATCTACTT[A/G]GATGTTCTTAAAACC | 10533 |
| rs116549451 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11452947 | GGAAGTGCACGATTC[C/T]GTGGGCTGTAGCGAG | 10533 |
| rs116550448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11547560 | ATTGTTGTACCATAT[A/G]GTAACTGTGTTTAAT | 10533 |
| rs116558557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11299626 | TTCACCACCTATTTA[C/T]CAGAGTCAATTAGGT | 10533 |
| rs116597392 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11437778 | TTCTCTTTTAAACCA[C/T]TTGAAAGCAAGTTTT | 10533 |
| rs116603513 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | ATG7 | GRCh38.p7 | 3:11382287 | ATACACATATATATA[G/T]AGAGAGAGAGTGCGA | 10533 |
| rs116654060 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ATG7 | GRCh38.p7 | 3:11462308 | AGGTGCAGCCACAAG[A/G]AGGAGACACAGGAGA | 10533 |
| rs116656478 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11519452 | GCTGACTCTTTCTTT[C/G]TCAGTGCGGAGGGGT | 10533 |
| rs116656503 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11322525 | ATATACAAACTTTTT[A/G]TATATTTCCTTTTAA | 10533 |
| rs116678263 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ATG7 | GRCh38.p7 | 3:11540809 | TTTTTTTCTCTTACA[A/G]TTCCTGCTTTTAGTG | 10533 |
| rs116681939 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11333309 | CAGGAAATTTTCTCT[A/G]GGCAGTTTTTTCAGT | 10533 |
| rs116684739 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11276722 | TCTCTCTGGCCATTT[A/G]TCCCTCAATTTCCAT | 10533 |
| rs116689724 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11336112 | TGGCAGGATCTCAGC[C/T]TACTGCAATCCTGGG | 10533 |
| rs116690337 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288069 | TGAGGCCTGCAGTGC[C/G]TTAAAATATTTACTA | 10533 |
| rs116714745 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11537304 | CATCATTCCACCTCT[C/T]ACCCCATTTTTTTCC | 10533 |
| rs116716865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457260 | CCCAAACTCTTGCGG[C/T]GGGAAGATCTGTACT | 10533 |
| rs116727071 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11311879 | ATTACAATTATTAGA[C/G]TTTCTCATCTGTACA | 10533 |
| rs116727951 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11361212 | AAAATAGGAGTGATG[A/T]GTAGGCTTGTCAGAT | 10533 |
| rs116741430 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11328002 | TTCAAGATAATGACA[C/G]TTCAGAGATGTTTTC | 10533 |
| rs116741604 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | ATG7 | GRCh38.p7 | 3:11467397 | TTCGTTTTGTTTTGA[C/G]ATGGAGTCTCCCTGT | 10533 |
| rs116741881 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11416867 | TCTAAGCATTTCTTT[C/G]CCTGCATCTCATGAA | 10533 |
| rs116767133 | snp | A/T | 0.000335656 | 0.0129505 | intron-variant | ATG7 | GRCh38.p7 | 3:11358380 | GATATTACCTATACC[A/T]TTGCTCCAGACATAA | 10533 |
| rs116799240 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11363128 | TGTGGCCACATTTCT[C/G]CATCTTTCCGGACAA | 10533 |
| rs116855941 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11544079 | GCTGCTCATCTGCCC[A/G]CACCAGCAGTCTGAA | 10533 |
| rs116883154 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | ATG7 | GRCh38.p7 | 3:11302941 | GCTGTCTTGAGTTAG[G/T]GTATCCTGCTGGATC | 10533 |
| rs116961397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11331608 | CTAGTGAACCTTAAG[C/T]AGGTCTGTTAGGGAC | 10533 |
| rs117038402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11538088 | GGAGATATGTGGACC[C/T]CAGGGCTGACAGATG | 10533 |
| rs117138184 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ATG7 | GRCh38.p7 | 3:11350671 | CGAGTCACAGGACCA[A/G]GCCCAAAGTCAATGA | 10533 |
| rs117140049 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557704 | TTTACTGTCTATATA[A/G]TTAATAGAAACCAGC | 10533 |
| rs117150978 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555408 | CACATGACCCAGTGA[C/T]GCCAGATTTCCACCA | 10533 |
| rs117243967 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11370778 | TGTGGCCAACTGGGC[A/C]TAATTGACTAAAGAT | 10533 |
| rs117359366 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11505951 | AAAGTCACTAAGCCC[C/T]TTTGAGAGCAAGATC | 10533 |
| rs117469272 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ATG7 | GRCh38.p7 | 3:11407773 | GGCCCCTTTCAGCCA[C/T]AGCTGGAGTGTCTGG | 10533 |
| rs117479023 | snp | G/T | 0.039522 | 0.134904 | intron-variant | ATG7 | GRCh38.p7 | 3:11514846 | CTGGTCTAGGTTTTT[G/T]TTTTTTTTTTTGGAG | 10533 |
| rs117526994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314326 | ATTCTTGAAACACAT[C/T]AATCACTAAAGCCCT | 10533 |
| rs117529977 | snp | A/G/T | 4.95252e-05 | 0.004976 | intron-variant | ATG7 | GRCh38.p7 | 3:11364608 | CTAGATCATCCTCCC[A/G/T]TGTGTTAAACTTGGA | 10533 |
| rs117545721 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11455010 | ATAGCCTGACTTACT[A/G]ATTTATAAAAGTTCA | 10533 |
| rs117549474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329528 | ACCCATTTATCCATC[C/T]ATCTACTTTTTTATC | 10533 |
| rs117569041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446263 | TTAAATTGGATTAAA[A/G]GTTACTATATCCATT | 10533 |
| rs117654276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305630 | GATGTCCTCATCTCA[C/T]CTGGATGAAAAATAT | 10533 |
| rs117725121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297911 | AGAAGGAATAACAGT[A/G]GTGCATCAGTCAGAC | 10533 |
| rs117726372 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11497866 | TATAGAGCCCTTTGT[C/T]GACATAAATGGTTCA | 10533 |
| rs117731772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11435863 | AAGGACATAAGAATA[C/T]GAAAAAGTGGGCCAC | 10533 |
| rs117805005 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11328147 | CTCACCACTGGAGAT[A/T]CTGAGTCTATCACCA | 10533 |
| rs117924897 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | ATG7 | GRCh38.p7 | 3:11357950 | AGAGGTCATGGTTTC[C/T]GTGAGCTATGATTGT | 10533 |
| rs117925206 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11551171 | CTCGTCGTGTCCTGC[A/G]GGCCGTCTGAGTGTT | 10533 |
| rs117961910 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287656 | TCAAATGAGCTTCGT[A/C]TTGGCTTAATGATGC | 10533 |
| rs118092106 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ATG7 | GRCh38.p7 | 3:11369629 | ATACAAGGAAGGATC[C/T]GGGTATAGGTCTAAC | 10533 |
| rs118122789 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11346373 | CTGGAAATAGGTCAT[A/G]GGATATGGGTATTCT | 10533 |
| rs118143873 | snp | A/C | 0.00730992 | 0.0600127 | intron-variant | ATG7 | GRCh38.p7 | 3:11306897 | CTTGTCTCTCCCTGG[A/C]TGAGTCCCAGCTGTG | 10533 |
| rs137884554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534574 | CGGGTGGCTACGTGC[C/T]GCCAGGCAGGGACTG | 10533 |
| rs137907131 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11375356 | AATGATTTAAATAGA[C/T]ATTTCTCCAAAAAAG | 10533 |
| rs137940571 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ATG7 | GRCh38.p7 | 3:11310109 | GATTGAGGCTGCAGC[A/G]TGCCATGATTGCACC | 10533 |
| rs137952109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11448893 | TCTCTCTCCCCTGCC[C/T]GACATTTTACACCAG | 10533 |
| rs137963741 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11295616 | TAAACATTAAATACA[A/G]TGTTTAAATGACCAG | 10533 |
| rs137975487 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11505250 | TTTAAAGGACGAGTA[G/T]GAGTTCTATAGGCCT | 10533 |
| rs137984314 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11338443 | GTAATAAAATCAAAC[A/G]AAATATCAATTAATG | 10533 |
| rs137989651 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11409890 | ATCAGTTGACTAAGG[G/T]GGGTCTAATTCTGGG | 10533 |
| rs137991052 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11484165 | TTGGGAGGCCGAGGC[A/G]GGTGAATCACTGGAG | 10533 |
| rs137999283 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11544328 | AAAAGCAGACCTGGG[C/T]CCAGCAAGGGAAATG | 10533 |
| rs138014414 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11429632 | ATAGATAATGCACTT[C/G]ATATAAAATTTAAAG | 10533 |
| rs138020281 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11396753 | CGCCACCGCACTCCA[G/T]CCTGGGCTACAGAGC | 10533 |
| rs138022096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326263 | TTCTCCCCCTTTTTA[C/T]ACTTGATAGAGTTGT | 10533 |
| rs138037755 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11529813 | AGTTGATGTCTCTGC[C/G]CGAAGGTACCAAGGA | 10533 |
| rs138052425 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ATG7 | GRCh38.p7 | 3:11367796 | TCTGGCCCAATGTAC[A/G]TGGATTAGATTCTGC | 10533 |
| rs138059886 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11468926 | GCCCCTCTGGCCCTC[C/T]AGGCTGTGTGTGGGC | 10533 |
| rs138063563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444480 | ACCAATTTTTGCTCC[G/T]TTGGGGGTGATATCA | 10533 |
| rs138072508 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11288941 | AGGCTTTCTTACACC[A/G]CTAGAGTTCTTGCTC | 10533 |
| rs138077981 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11504760 | AAAACAATGTTGTAC[A/C]AGAAAGAATAAGTAA | 10533 |
| rs138080716 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11493608 | ATGGGTGATGCTAAA[C/G]CAGGATGAGTAGTAA | 10533 |
| rs138107536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500472 | AAATACAAATTAAAA[G/T]ACTAAAAACTAGAAA | 10533 |
| rs138116321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421452 | ACCACTCTCTTTGCT[C/T]ACCTGTAAGAAGCAA | 10533 |
| rs138119273 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11491848 | GTTTTGTCTCAGAGG[A/C]GTACCCGGCCGTGTG | 10533 |
| rs138134486 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11320076 | CTGTGGGCATCCAGC[C/T]CCAAGTCATTCCGTG | 10533 |
| rs138143676 | in-del | -/TTG | 0.120327 | 0.220522 | intron-variant | ATG7 | GRCh38.p7 | 3:11326294 | AATGCTGTTTTTTTT[-/TTG]TTGTTGTTGTTGTTT | 10533 |
| rs138145922 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11440812 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 10533 |
| rs138178997 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11525744 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 10533 |
| rs138191276 | in-del | -/AAAAG | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11517466 | TTGAGGCAGTGAATT[-/AAAAG]AAAAAAAACTCGATC | 10533 |
| rs138191787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361373 | CCCTGCAACCTCTGC[C/T]TCCTGGGTTCAAGTG | 10533 |
| rs138222127 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11548597 | TGCAAAATTAAAAAC[C/T]TTTTTTTCTTAAACA | 10533 |
| rs138246308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11468129 | CAGCTATAGAAGAGC[A/G]TGACTTTCATCCCTG | 10533 |
| rs138253426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547082 | CTATTGTGCATTTGC[A/G]TGACAGGCGGTGAAT | 10533 |
| rs138259524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313601 | GTCATTTTTTTGTAT[A/T]TATATTTATATATGT | 10533 |
| rs138300836 | in-del | -/A | 0.0872718 | 0.189788 | intron-variant | ATG7 | GRCh38.p7 | 3:11506039 | ATGGGAATGCTTTGT[-/A]AATAGAACATTTCTG | 10533 |
| rs138320273 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11386956 | ACCTTGGACATTTCT[C/G]CCTTTGCTTCTATTT | 10533 |
| rs138325414 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11278867 | ATACAGGAGGATCGA[C/T]CTAATCCAGAGCTGA | 10533 |
| rs138327470 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11329463 | GGTTCTCTGCCAGCA[A/G]TTTCCCTCCCTCACC | 10533 |
| rs138328992 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11306262 | AGAGCCCTGTTTGGG[A/G]TGGGCTAGGTTGTGG | 10533 |
| rs138334491 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11466288 | GAGACATAAATATGT[G/T]TTTCCCCTCTTAATT | 10533 |
| rs138339330 | snp | A/G | 0.00184724 | 0.0303349 | intron-variant | ATG7 | GRCh38.p7 | 3:11379950 | TGTTTGATGTGAATT[A/G]TTTTGTTTTGTTTGT | 10533 |
| rs138376531 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11414562 | TGTCTTATTTCATTA[C/G]CTAGGCCTTCTATTA | 10533 |
| rs138400147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335206 | TAGCACCCTCTCCTG[A/G]CAAATTCTAAAATAG | 10533 |
| rs138409801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11344467 | ACTACGTTTATCAAG[A/G]CAAAGTATTCTAATG | 10533 |
| rs138440666 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11410355 | AAATTAAAATTTGAT[A/G]GTATTTGAACATCAA | 10533 |
| rs138446905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461413 | TCCTGCTTAGAATTT[C/T]CACGGCGTCTTTTCT | 10533 |
| rs138448027 | snp | A/C/G/T | 0.000691878 | 0.0185878 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347974 | TTGAAGATTGCCTAG[A/C/G/T]GGGTGGTAAGCCCAA | 10533 |
| rs138449360 | snp | C/G | 0.00111692 | 0.0236075 | intron-variant, missense | ATG7 | GRCh38.p7 | 3:11510278 | TGTCCTGAAATAGAT[C/G]TCTACCAGCTCTCAA | 10533 |
| rs138450163 | in-del | -/A | 0.0569829 | 0.158885 | intron-variant | ATG7 | GRCh38.p7 | 3:11331220 | TTAGCCCTTTACCAG[-/A]TGTTTAATTTTTAAG | 10533 |
| rs138452866 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11519721 | CCCGTCACCGCGCCC[A/G]GCTAATTTTTTTTGC | 10533 |
| rs138470616 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11516941 | TCCACAAATTAGCCG[A/G]GTATGGTGGCACGTG | 10533 |
| rs138479259 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11376031 | AATTGAATATTATTT[A/G]GCAGTAAAGAGGAAT | 10533 |
| rs138480282 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11544753 | CACACCAAAAATCCC[C/T]CTTTCTTTTCTGCCC | 10533 |
| rs138489822 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11452824 | GTGTTAAGACCTATT[A/C]TTTTTAGTATTTTTT | 10533 |
| rs138511862 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11505010 | AACCTGAAAAGATCG[A/G]GAAGTCAAGAGGTGA | 10533 |
| rs138541463 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11352618 | CTTATTCATCACCTT[C/T]CTTCTACCAGGCCAC | 10533 |
| rs138563683 | in-del | -/CTGT | 0.067446 | 0.170804 | intron-variant | ATG7 | GRCh38.p7 | 3:11530428 | AGTGTAGCTTCCAGA[-/CTGT]CTTTCATCAGTTTTG | 10533 |
| rs138568777 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11304734 | AGCAGGCCCAGTCTT[C/G]CGGCCTTTGTGAGAT | 10533 |
| rs138578039 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11283863 | CTTGAACCCGGTAGA[C/T]GGAGGTTGCAGTGAG | 10533 |
| rs138599719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11348402 | TCCTTCCAGTGGGTT[C/T]GTGGGGTTCCTTCCG | 10533 |
| rs138599786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11301060 | GGGAGGTGAAAGATG[A/G]TACAGAACTAGCGAA | 10533 |
| rs138600664 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11483646 | ATCCTTGTATATAGA[A/G]GTGGAGCTTAATCTG | 10533 |
| rs138604622 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11400246 | AAGAGACTGAGTCCA[A/T]TGTAAGTTTTCAATA | 10533 |
| rs138614183 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11495994 | CAGGCACTTTCCACA[C/T]GGTAGCCCTATGACG | 10533 |
| rs138634976 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11534203 | GAACTGGAGATTCCA[C/G]CAGCACCCTAGGTCT | 10533 |
| rs138651108 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11368971 | CTCAGCTTCATGAAT[C/T]CTTTTAGCTTCAGAA | 10533 |
| rs138653440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448554 | ACCAAATCTGTAATC[A/G]GGAACATAAACCAAC | 10533 |
| rs138656703 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11289636 | CATGGATCACTGCAG[C/T]CTCAACCTCCTGGTG | 10533 |
| rs138656754 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11408379 | AGTTCCAAACTTTCC[C/T]ACATTTTGCTGTCTT | 10533 |
| rs138659601 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11362698 | GGATGTTCTTTGCCA[A/G]CAATGAGCATCTGGT | 10533 |
| rs138663332 | in-del | -/TGAAT | 0.398534 | 0.201091 | intron-variant | ATG7 | GRCh38.p7 | 3:11413597 | AACTGACTTAATAAA[-/TGAAT]TCAGCAAAGTAGCAG | 10533 |
| rs138683677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461801 | GGAGGCCGAAGCGGG[C/T]GGATCACGAGGTCAG | 10533 |
| rs138687864 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11404589 | TGTGGTTTTGGGCAT[A/G]TACCTAGCCTTGTGC | 10533 |
| rs138709662 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11512558 | AATGAAGCCATGGAC[C/T]GTCGCAGTGAGTGTT | 10533 |
| rs138710852 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11359200 | AGAAAGAGAGGGAGA[A/G]TATGGGAGAGAAAGG | 10533 |
| rs138715397 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11476311 | CAGTTTGTAGAAAAT[A/G]GGCACAATTCTAGGA | 10533 |
| rs138716080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11382725 | GAATTTCCTGTAGTG[C/T]ATTAAATTACTTTGT | 10533 |
| rs138724586 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557299 | CTGCCTTGGCCCCAG[C/T]GTACGAGGAAGCGTA | 10533 |
| rs138733297 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11494740 | GGGCTTTGGCAGCCA[-/T]TTGTCAGAGGTGTTG | 10533 |
| rs138747256 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11472069 | TCAAGATTAAACTCT[A/G]CAAAATTATTATATT | 10533 |
| rs138748477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509013 | ACAAACAGATCCCTT[G/T]AGCAAATGCCCTTTA | 10533 |
| rs138766562 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11397011 | AAAATTGAAAAAGAT[G/T]ATTTAAAGGAAGAAA | 10533 |
| rs138771506 | snp | A/C/T | 0.000149711 | 0.00865079 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362869 | TCGTCCAGGACTGGC[A/C/T]GTGATTGCAGGAGCC | 10533 |
| rs138793693 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11520551 | GATGAGGAAGATGCC[A/G]TGCTGGCCCTGGAGG | 10533 |
| rs138799304 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11525899 | CTAGCAGCTGCTGAA[A/G]AGTTCTGTCACCTTT | 10533 |
| rs138847366 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11325626 | TGGTGAGCTGAGATC[A/G]TGCCATTGCATTCCA | 10533 |
| rs138858285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457602 | ATCAGGGGGAAACAT[A/T]TCCGGAACATACATT | 10533 |
| rs138866369 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11367133 | CCCATGTATAGGCTT[A/T]AAACAACTTTTTTCC | 10533 |
| rs138874336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515874 | TTGAAAAAAGCAGTG[C/T]TGTGGGGCTTGAAGC | 10533 |
| rs138895550 | in-del | -/GAAT | 0.314787 | 0.241459 | intron-variant | ATG7 | GRCh38.p7 | 3:11553404 | AATGGGAGAGTGAAA[-/GAAT]GGATGGATTGTGCTG | 10533 |
| rs138937635 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11293595 | GCTCACATCTGTAAT[C/G]CCAGCACTTTGGTAC | 10533 |
| rs138946299 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11305218 | TTCCTGCCACCTCCC[A/G]TGGTGGAACTTTAGT | 10533 |
| rs138947730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11345005 | AAAATAAACTTAAAA[C/T]GTTCTGCCTTTTTCT | 10533 |
| rs138991457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11359883 | TGTGAACATGACAGT[A/G]TAGCATAATGGTGGA | 10533 |
| rs138997771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464516 | CTGGCAGCCTGGTTC[C/T]TAGGACACCAGCACA | 10533 |
| rs139028903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415956 | CCACAAACATGGAAG[C/T]AATGTTGTTGCACTA | 10533 |
| rs139029318 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11432512 | GAGAAGCTTGGGAGG[A/G]GGGGTAAAGGATAAA | 10533 |
| rs139031272 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11310792 | CACCCACCACCACAC[C/G]CGGCTAATTTTTTGT | 10533 |
| rs139033291 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11357298 | GTGCCAAAATATTAT[G/T]TGGTCATCAAGGGGC | 10533 |
| rs139040449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11494258 | CAGGAATTAGGGAGG[A/G]GTAAGGAAGAGGAGT | 10533 |
| rs139050477 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11437057 | GATGAATCATATGGT[A/G]TGTGAATTATCAATA | 10533 |
| rs139052905 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352941 | AGAAAATTGGCCTTT[-/T]GAAGGTAAGAACTGT | 10533 |
| rs139056501 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11497051 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10533 |
| rs139063012 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11397582 | CCTGCCTCAGCCTCC[A/G]AGTAACTGGGACTAC | 10533 |
| rs139065393 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11472647 | TTTTTGTTGCTAATA[C/T]GTCTGTTATTTCCTA | 10533 |
| rs139071704 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11428270 | AATGAATAGATGGCC[A/C]GGCCCAATACTGGAC | 10533 |
| rs139072103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11353165 | GTTTAAATTTTGGGC[C/T]GGGCACAGTGGCTGA | 10533 |
| rs139125699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528394 | CAGTCACCAATATCC[A/G]GGAAGTCAGATGGTC | 10533 |
| rs139129280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459428 | ACAGATTTAAGATAG[C/G]TATACTCAACATCAT | 10533 |
| rs139131283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11517791 | AGAGCTGGAGAGAGT[C/T]GGGCAATTGAGTTGA | 10533 |
| rs139142913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11431134 | GGCTGGGCGCAGTGG[C/T]TCACGCCTGTAATCC | 10533 |
| rs139152833 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11553506 | CCTAAATGCAACCTT[C/T]GTTAGAAACACAGCT | 10533 |
| rs139188736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531236 | GGGGCTGTGCAGGGT[A/G]CCCAGCCAAGGCAGA | 10533 |
| rs139210553 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11480992 | ATAAATTACTCTTAA[G/T]TCTTCTAGGCAAGGG | 10533 |
| rs139213736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541460 | GCTGCCTGAAGCTTT[A/G]TAGAGTCAGTGGGTC | 10533 |
| rs139229164 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527264 | CACATGCCACCACAC[A/C]CAGCTAATTTTTGTA | 10533 |
| rs139230407 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11273638 | TATTATATATGCTCA[A/G]TAAATATTTGTTGGA | 10533 |
| rs139243557 | in-del | -/TTG | 0.166506 | 0.235645 | intron-variant | ATG7 | GRCh38.p7 | 3:11314414 | TTGATTAAATTTTTT[-/TTG]TTGTTGTTGTTCGTA | 10533 |
| rs139272619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298356 | AAGTAGAATGGTGGG[C/T]GCAAGGTCCTGGGGG | 10533 |
| rs139301159 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11275323 | CATGGAAATGACGTT[C/T]GCTAATGTCTTCCTC | 10533 |
| rs139308795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311145 | CCTTGTTTACTGAGC[A/G]TTCTTAGCCTGACTT | 10533 |
| rs139319177 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11341009 | CGTACCTGTACTGCC[A/G]TTCAGTCCTTTATGC | 10533 |
| rs139338040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11323271 | GAAGTCCTGGAATGC[C/T]GAATTGAAAAGAGAC | 10533 |
| rs139359768 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11470210 | AGTGTGGCACCTCTG[C/T]AGTCACACATCACTT | 10533 |
| rs139360953 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11315011 | GTTCGGGGTAAAATT[C/G]ATCAGGGGTAGATTC | 10533 |
| rs139363611 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11531484 | GCATTAGGGTGCTCA[C/G]CTCTCTGTAGATTTC | 10533 |
| rs139374430 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11370648 | GGCATTGGATCTTAG[C/T]CTCCCATCGAGGCCT | 10533 |
| rs139375411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290407 | TTTACTGGGCTCAGA[C/T]CAGGAGCCCATGGTC | 10533 |
| rs139403962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11481464 | ACTTACCACAAAGAC[C/G]TAGAATTTCACATTT | 10533 |
| rs139420963 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11405704 | GTGATCATGGCTCAG[C/T]GCAGCCTCAACTTCC | 10533 |
| rs139426538 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11387953 | CCAGCCTGAGTGACA[C/G]AGCAAAAGAAAAAAT | 10533 |
| rs139446360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11424014 | TCAGGGTCACCACTC[C/T]TCTCAAGCCCCATAG | 10533 |
| rs139446658 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11492308 | GTGAGGCAATGCCTC[C/G]CCCTGCTTCGGCTCG | 10533 |
| rs139457502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323932 | ATTAGCATGTTTTAT[A/G]GGATCATTGTGGAAA | 10533 |
| rs139472290 | snp | C/T | 6.68695e-05 | 0.00578189 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333038 | GCAGGGGGCGAGAGA[C/T]GTTGCCCACAGCATC | 10533 |
| rs139477323 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11363855 | AAAGCTTTCCTCAGC[A/G]GTTGAAAATTGTGGT | 10533 |
| rs139483153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11440967 | GAGATATAGGCATGA[A/G]CCACTGTGCCTGGCC | 10533 |
| rs139491963 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11327593 | ATTGCTGCAGACAAT[C/G]AAGAAGTTTGTAACT | 10533 |
| rs139529560 | in-del | -/C | 0.234982 | 0.249549 | intron-variant | ATG7 | GRCh38.p7 | 3:11548792 | TGAGGGCCTCTTGGG[-/C]CCTGTTCCCAGTCTT | 10533 |
| rs139547459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387549 | TCAGGGTATTGAAAA[A/G]TTGGGTTCCTTTTAG | 10533 |
| rs139564364 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11374488 | AAATTCCTAGAAGAA[A/G]ATATCATAAATCTTT | 10533 |
| rs139568993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11316600 | TACAAGTTTCTTTTT[A/G]TGCCATATTAGACTG | 10533 |
| rs139583683 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11325125 | TACCAGGTAGCCCAG[A/G]TGTGGTGTAGTAGGC | 10533 |
| rs139583762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369584 | CCATTTGGATGTAGT[A/G]GAGTCTGGTTCCAGT | 10533 |
| rs139590023 | snp | A/G | 1.66277e-05 | 0.00288333 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315385 | TAATCTTTGTCAAAC[A/G]GAAGGAGTCACAGCT | 10533 |
| rs139624584 | in-del | -/ATTATTATTATT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417784 | ACCAGCATTTAAAAA[-/ATTATTATTATT]ATTATTATTATTATT | 10533 |
| rs139626178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380950 | CCTTTGAAAACTGTA[C/T]TTGGGCTATATTTTA | 10533 |
| rs139642990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542918 | CTAGCTCCTTGTCAG[C/T]TGCAGCCCTGAGCAT | 10533 |
| rs139648970 | in-del | -/TA | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11496835 | CCATAGGCCTTTCCT[-/TA]TGTCATGTCTTTTTA | 10533 |
| rs139671541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492143 | GGACCCTCCGAGCCA[G/T]GTGTGGAATACAATC | 10533 |
| rs139677572 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11545406 | ATCCTTCTCTTGTGG[C/G]CATCGAGAGCCTGCG | 10533 |
| rs139694731 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11295939 | ATGTGCCACCACACC[C/T]AGCTAATTTTGTATT | 10533 |
| rs139707229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336498 | TTCATGTAAATTAAT[A/G]TGTTCCCTCTTAGCT | 10533 |
| rs139724418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339619 | TTCCACCAAGGCAAG[C/T]AAAGCTTTCATTAAC | 10533 |
| rs139743451 | in-del | -/AG | 0.397271 | 0.202018 | intron-variant | ATG7 | GRCh38.p7 | 3:11400841 | TTACAAACGTCACTC[-/AG]GGTAATAATTTTCTT | 10533 |
| rs139743872 | in-del | -/AAAC | 0.498525 | 0.0271165 | intron-variant | ATG7 | GRCh38.p7 | 3:11392463 | GGGAAATCATTAAAA[-/AAAC]AAACAAACAAAAAAA | 10533 |
| rs139758268 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490406 | ATACAGCACACTGAT[A/G]AGTCTTGACTCTTTA | 10533 |
| rs139763166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454622 | TTTCTGGGCATATGA[A/G]GCCACATTTCCCTTT | 10533 |
| rs139770731 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11336314 | GCTAGGATTACAGGC[A/G]TGAGTCACACGTCCA | 10533 |
| rs139786374 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270818 | GAAACAAATCACAAT[G/T]GTGGAATGTCATCAG | 10533 |
| rs139786948 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11393337 | TGCTTTTGTAATAGC[C/T]ACACCTGGGGTATGC | 10533 |
| rs139791885 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11351924 | TGTTACATATGTATA[C/T]ATGTGCCATGTTGGT | 10533 |
| rs139792582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11377324 | ACTTCATTTTCTGGG[A/G]AAATAAATCTGTTTC | 10533 |
| rs139796103 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11469372 | GATAATTGCTTGAAC[C/T]CGGGAGGTGGAGGTT | 10533 |
| rs139797576 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11522803 | CTCTGAGCTTGTGGT[A/G]CAGACTGTGAACATG | 10533 |
| rs139815139 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11501125 | CAGGTATGGTGATAC[G/T]CACCTGTAGTCCCAG | 10533 |
| rs139815563 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467359 | TGGACATAAAATATT[A/G]CCTCAACCGTAATTT | 10533 |
| rs139838084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11388629 | GAGACAGGGTTTCAC[C/T]GTGTTAGCTAGGATG | 10533 |
| rs139861440 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11497739 | GCAACTTTGGTACAC[A/G]AGGCTGGTTTTAGTT | 10533 |
| rs139871909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11286065 | TATCTGATGTTTCCT[C/T]CCATGAGATCCAGGT | 10533 |
| rs139894216 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11498033 | GTCCTCATTTTAAGA[C/G]TGATGTTGAGGGCTA | 10533 |
| rs139895592 | in-del | -/TC | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11477446 | AGCATCAGCATGTTT[-/TC]TCTCCCTCTAATTTA | 10533 |
| rs139908352 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11332293 | CTAAAATAATACATA[C/T]TCCATGATTCCATTT | 10533 |
| rs139924097 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11402258 | CCAACATGGTGAAAC[C/T]CGGTTTCTACTAGAA | 10533 |
| rs139955127 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11279817 | CTCCTATAACATTCT[A/G]TACAAACGCCAGGCT | 10533 |
| rs139962054 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450256 | TTGGCTCCAGAGCCT[A/G]TGTTCTTAACTACTA | 10533 |
| rs139966854 | snp | C/T | 1.65501e-05 | 0.00287659 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554814 | TTCTCCATGCAGATC[C/T]GGGACATGAGCGATG | 10533 |
| rs139984119 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11354256 | TACATGAAAAGAAGC[A/G]CTCTGCTACAGATAC | 10533 |
| rs139991822 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11383128 | CAGTCTGTGTATTCA[A/G]TGTTGTTGTTTATAC | 10533 |
| rs139998159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371489 | TTGCTGCATGGAGAA[C/T]AGACTGGAGGTGATA | 10533 |
| rs140004139 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11410647 | TCCCTCATAAGTAGA[G/T]TCATACATTATTTGT | 10533 |
| rs140005853 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11484707 | CCTCCCCTGACCCCA[C/T]GACAGTCCCCAGAGT | 10533 |
| rs140026663 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11482166 | TCCTTCCAACTGGAA[A/T]GTTCATGAGAGAAGT | 10533 |
| rs140050179 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11406673 | TGGCTGGGGAGGCCT[C/T]ACAATCCTGGTGGAA | 10533 |
| rs140073666 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11514327 | CAAGAGAAGCATAAT[A/T]AACTTTGAAGATGGG | 10533 |
| rs140075103 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11327934 | GATGCATGCTGCTGG[A/G]GCATGGACCACATTT | 10533 |
| rs140080336 | in-del | -/CT | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11357420 | GAGAGTGAAGCCTTA[-/CT]CTGTCCCACACTCTG | 10533 |
| rs140084978 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11505596 | TCCTTACCTCCGACC[A/G]CAAAAGAGTCTTCTA | 10533 |
| rs140134677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446071 | CCAGCGACCTTTGTT[A/C]TAATCCCAGATGTTT | 10533 |
| rs140164462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11302164 | AATAGCCCTGGATTC[A/G]AAGTTTGAAGATTTG | 10533 |
| rs140177486 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11442922 | CAAGACCTTGGCTGT[A/T]CAACAAACAAAACAA | 10533 |
| rs140177868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11502870 | AGCTTTTGTGCAATA[A/G]GACAGACAACTGCCC | 10533 |
| rs140183262 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297600 | TCAAATTTATTAGAT[G/T]ATTCGAAGGGGGAAA | 10533 |
| rs140183559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542135 | CGACAGGAGCCACTG[A/C]TCTTGAAACCTCCCT | 10533 |
| rs140186733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457586 | CATTCTTTGCCTCCG[G/T]ATCAGGGGGAAACAT | 10533 |
| rs140211662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311772 | TAGGACTAGACAGTT[C/G]ATTAATTTCAGCTTT | 10533 |
| rs140218432 | snp | C/G/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11538807 | TGAGCCTGGGAAGGT[C/G/T]GAGGCTGCAGTGAGC | 10533 |
| rs140219798 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272673 | CTGACTTGGAAGCTC[G/T]TGCTGATTTCCTAAG | 10533 |
| rs140236981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551469 | TCTACTCCAGTTTAC[A/G]TCTTTCCAGGAGAGA | 10533 |
| rs140249943 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11309250 | ACCAATGCTAACTTA[A/T]TTCACCCCTATGGAT | 10533 |
| rs140255841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288557 | GTTATTTCTGTATTG[C/T]TTTATATACATAATA | 10533 |
| rs140280448 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11425095 | AGCTTCCCAAGTAGC[G/T]GGAATTACAGGTGCA | 10533 |
| rs140301517 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11403265 | GAGTCTTTTGGAGTG[C/T]GGAGAGGAAGTCCTC | 10533 |
| rs140324924 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11483003 | ACCTCTATCACCCTA[A/G]TTACTTGGGATTCTC | 10533 |
| rs140325730 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11367328 | AGGAACTTGGTAAAC[C/T]CCTTTGTGTACTTTG | 10533 |
| rs140345243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479546 | TAGTCCAAGTCCACC[A/C]GCCCAGAATCACCCT | 10533 |
| rs140366504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285698 | TGATTGGTTTTGCCT[C/G]TTGAACAACGTATAA | 10533 |
| rs140369287 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11536644 | CTGGCGGGGAGTCCC[A/G]AGAGCGGACCCTCTT | 10533 |
| rs140370081 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420941 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 10533 |
| rs140390221 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ATG7 | GRCh38.p7 | 3:11511795 | GCACCGGTGGGCTGG[C/T]ACTGCTGGGGTACTC | 10533 |
| rs140400695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347335 | CTATTTCTAAGAATA[C/T]AGACTTGTTCCCTAA | 10533 |
| rs140406205 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11281603 | TATAGTGAAACCCTA[C/T]CTCTACTAAAAATAC | 10533 |
| rs140411782 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486201 | CTTCCATTTGTTTGT[A/G]TCCTCTTTTATTTCA | 10533 |
| rs140421968 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11361299 | TTCTTTTTTTTTTTT[C/T]TTTGAGACAGAGTTT | 10533 |
| rs140424673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401376 | ATAATATCTTTGGTT[C/T]GGCTTATGTCAGTCA | 10533 |
| rs140463248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11417220 | TTTGAGTTCAAGTGC[A/G]TCCTTTTTAACCTTC | 10533 |
| rs140496961 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11507608 | CTCCATTATAAGTGA[A/C]GGAAATGCTAAAGTT | 10533 |
| rs140515587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522660 | GACTAAAATTCTAGA[A/G]GTCATTTATACCAAA | 10533 |
| rs140525279 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11356190 | AAGACCATGTTCTGG[C/T]GTCATGAAAATGTTC | 10533 |
| rs140530187 | in-del | -/ATTA | 0.499776 | 0.0105807 | intron-variant | ATG7 | GRCh38.p7 | 3:11424605 | TTAATTTTAATAAAT[-/ATTA]ATTTTTAATATTAAA | 10533 |
| rs140533169 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11431372 | TGCTGTTGCACTCCA[G/T]CCTGCAAGGGCGGGG | 10533 |
| rs140554346 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11463153 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 10533 |
| rs140559603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329088 | TAATAACGGTAATAA[C/T]GTGAGACTCTGTCTC | 10533 |
| rs140592252 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11459892 | GATGCTATTCTAACC[A/G]TATTAACATATTAAA | 10533 |
| rs140597358 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11371590 | CATACCTGGCCTTCC[A/C]TCAGAATCACCTAAG | 10533 |
| rs140599190 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447116 | CCTTTTGTAGCCATC[C/T]ATACCCTGGTTACAA | 10533 |
| rs140600347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518086 | GTGGGAGAGAGGAAG[A/G]GGACCAAGGTGCTTC | 10533 |
| rs140608347 | snp | C/T | 1.65179e-05 | 0.00287379 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313319 | GATCTAAAGAAGTAC[C/T]ACTTCTACTATTGGT | 10533 |
| rs140619582 | snp | G/T | 1.65296e-05 | 0.00287481 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11340699 | GAGGCATGGGACCAA[G/T]GATGGTGAACCTCAG | 10533 |
| rs140632796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465800 | CTGTAGCCCCTCTTC[A/C]TTCCCTAATATATTT | 10533 |
| rs140640020 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11554736 | CTGCCATGACTGCTG[C/T]GGTTTTGAAGCATCT | 10533 |
| rs140649612 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11382283 | TTATATACACATATA[G/T]ATAGAGAGAGAGAGT | 10533 |
| rs140668478 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11492588 | TCGCGGGAGGGAGCA[C/T]GTGAATGAATAAGTT | 10533 |
| rs140670402 | in-del | -/TGATT | 0.107694 | 0.205546 | intron-variant | ATG7 | GRCh38.p7 | 3:11400580 | TAATGTGCAAGTACC[-/TGATT]TTTAAGTGTTGGTTC | 10533 |
| rs140670708 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | ATG7 | GRCh38.p7 | 3:11486830 | GTTCTGTTTTTTTTT[G/T]TTTTTTTTTTAATTT | 10533 |
| rs140675250 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11556004 | CATGGGGACACAGCC[A/G]GCACAGGTGCAGGGC | 10533 |
| rs140694847 | snp | A/C | 0.040671 | 0.13668 | intron-variant | ATG7 | GRCh38.p7 | 3:11551789 | GGTCTCACCCTGTCG[A/C]CCAGGCTGGAGTATA | 10533 |
| rs140710668 | in-del | -/A/ATTA/ATTATTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417802 | ATTATTATTATTATT[-/A/ATTA/ATTATTA]TTATTTTATTTTATT | 10533 |
| rs140714814 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | ATG7 | GRCh38.p7 | 3:11491489 | TCAAAGTCATTCTCC[A/G]TCCAGCTTTGTTCCA | 10533 |
| rs140745616 | snp | G/T | 0.000264581 | 0.0114987 | intron-variant | ATG7 | GRCh38.p7 | 3:11307081 | CTGTGAAAACGTGAT[G/T]TATGTGTCATATTTC | 10533 |
| rs140746761 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11375638 | GATCGCAGCTCACTG[C/T]AACCTCTGCCTTCCG | 10533 |
| rs140767378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414427 | GTGTTGCTGTGATTG[C/T]GTGTTAGTTCCAACA | 10533 |
| rs140776728 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11486709 | TATTTTGAGATATGT[C/T]CCATCAGTACCTAAT | 10533 |
| rs140788185 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272171 | TTAAAAGCCTGAAGG[G/T]AATGTAGACATTCCG | 10533 |
| rs140795876 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11518675 | ACATCTGGGAGTTGC[A/T]GGATTCTAGAATAAA | 10533 |
| rs140804067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11329481 | TCCCTCCCTCACCCC[C/T]ACTCACTCTACATCC | 10533 |
| rs140830123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448518 | AAAAACTTACTTGCC[A/G]TGCTGAAACTTGTTG | 10533 |
| rs140838862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422328 | TAGATCTCATAATAA[C/T]ATGTTGCAGCTTCTA | 10533 |
| rs140839001 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11350976 | TCTATCGTTGGAGAG[C/T]ATTATGAACTCCCTT | 10533 |
| rs140840348 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11534071 | AGCCAGCAGAAAGCC[G/T]CCTCCTCCCCCCCCA | 10533 |
| rs140850243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347823 | AGATTTCAAGAGACA[C/G]CACCCTGTGAAATGT | 10533 |
| rs140851496 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11372308 | TAGTTTAGGCGTACA[A/G]TTTTTTTTTTCTAGA | 10533 |
| rs140857608 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11543152 | TCGTTTTCTCCTTTT[A/C]ATCTCCTCATCCCTG | 10533 |
| rs140875856 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11442033 | GTCTTGAACTCCTGG[A/C]CTCAAGCCATTCACC | 10533 |
| rs140879526 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11364958 | CCAGAGTCTTTGATG[C/G]GTTTTGTAAACTGAC | 10533 |
| rs140888998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11384898 | CCAGAGGTTGAGATC[A/G]TGCCATGGCACTATA | 10533 |
| rs140889016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343357 | GTTAAGTAACATTTA[C/T]TGTTTGAATTTGTGT | 10533 |
| rs140896550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11464783 | TCTGACCCCCTATTT[C/T]CAAATTATAGCTCTA | 10533 |
| rs140896914 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11308119 | AAACTGGGGGCCTCT[C/T]TTCAGTGGTCCAGCT | 10533 |
| rs140920220 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11427623 | GAGTTTGAGACCAGC[C/G]TGGCCAACATAGTGA | 10533 |
| rs140932960 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11537738 | CCTGCTCGGTGCCAG[C/G]TTCTGGGTCTGTGCT | 10533 |
| rs140937534 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11443493 | CAAGCTCAAGTGATC[C/T]TCCCAACCTCATCCT | 10533 |
| rs140948817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11528215 | TTTATAGCCTGCAAC[A/G]ATATTGACTTCATTC | 10533 |
| rs140966732 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11478248 | CAAACTTAAAAAAAA[A/T]TATTTAAATGTTTTC | 10533 |
| rs140987655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11539685 | TGTGAAACTCCCCCC[A/G]TCTTAAGCTATATTC | 10533 |
| rs141005188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11474748 | TTCTGAGCTGAGCCC[A/G]GAATGCAAAGAAAGG | 10533 |
| rs141020269 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535432 | AAAGTCTTCTGCGTC[A/G/T]GCCCTCCCTGAGCAG | 10533 |
| rs141020810 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11388757 | TTTATTCATATAGTA[C/G]ATTCATCTTCATCCT | 10533 |
| rs141027703 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11508677 | GCTGGTCTCCAACTC[C/T]TGGGCTCAAGTGATC | 10533 |
| rs141086338 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11413360 | CCTAGTTTAAGTGTT[G/T]TTATCATGAAAGGGG | 10533 |
| rs141117221 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11493022 | CACCAGCAAGGGCAA[A/G]GGGCCAGTGTGACAG | 10533 |
| rs141129427 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11408598 | TTACAGTTCCACATG[G/T]TTGGGGAGGCCTTAC | 10533 |
| rs141134239 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11397144 | AGATTATCAAACCAG[A/G]TTTTTAAATTTATAT | 10533 |
| rs141136251 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11327320 | GTCAGGAATTTCTTA[C/G]AATTGTGTATATTTA | 10533 |
| rs141143773 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11518329 | AGGTGGGTGGATCAC[A/G]AGGTCAAAGAGATCG | 10533 |
| rs141154576 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445094 | AAGGAACGCTTATAC[A/G]CTATTGGTGGAAGTG | 10533 |
| rs141155261 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11540562 | GGGAGGATCCCTTGA[C/G]ACCAAGAGGTGAAGG | 10533 |
| rs141162998 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11505060 | TAACATACAGAGGTA[A/C]CTAAAAGTATCAGGT | 10533 |
| rs141170885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338038 | TCCCAGGGGTTTGTT[G/T]TACAGATTATTTGAT | 10533 |
| rs141210616 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11291048 | GAAGTGCTGTAGAAT[A/G]GAGTTTTCTTTTTTG | 10533 |
| rs141243011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11391063 | CTGTCAGTGTTTTCC[A/G]TTGATCTTTTGTCTG | 10533 |
| rs141247907 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287867 | CCTCAAAACAAAATA[C/T]ACTATTGGCACCTTC | 10533 |
| rs141266781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11499828 | AGGGCACCTCCACAC[A/G]CAGTTTGGGAGCCAC | 10533 |
| rs141268212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366354 | TGAAAACCACAAAAC[A/C]CTATGAAAATGTGCC | 10533 |
| rs141285073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402987 | AAAACCAGGAATCTA[G/T]TCTCTTAAATGCTTA | 10533 |
| rs141294452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478949 | TACTACCTGAACACA[A/C]AAGGAGAAATAAACT | 10533 |
| rs141326561 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11348550 | TGGGTTCATAGTCTC[A/G]CTGACTTTAAGAATG | 10533 |
| rs141334951 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11279973 | TGAACCCTGAAATGT[A/G]GCACAGGGACAAGTA | 10533 |
| rs141336500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420319 | TCCAGCATTAAACTT[C/T]CTGTACATCCTCATT | 10533 |
| rs141356566 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11465426 | CTCCAGCCTGGGTGA[C/T]AGAGAGAGACTCTGT | 10533 |
| rs141356706 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11524241 | AGCTGAAGTTGAAAC[A/T]CAGACAAAGGAAGGC | 10533 |
| rs141360289 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | ATG7 | GRCh38.p7 | 3:11303882 | ATCGAGACCATCCTG[C/G]TTAACACGGTGAAAC | 10533 |
| rs141375959 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11519813 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 10533 |
| rs141381398 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11431884 | GCACATAGTAATGAA[-/T]TTGGAAGCCATATCC | 10533 |
| rs141423964 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11374840 | ACCCAGGAGGCGGAG[C/T]TTGCAGTGAGCTGAA | 10533 |
| rs141445372 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11458831 | TTAGGAACCCGATCG[C/T]GCAGCTGTAGGTGAG | 10533 |
| rs141452229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299160 | TTTTATATTCTTGGC[A/G]AATGTCTCATATTCA | 10533 |
| rs141456619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11353240 | CGAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA | 10533 |
| rs141459586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11274786 | CTGTACGAGGTGATA[C/T]GTTACTCACTTGACA | 10533 |
| rs141468501 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11486036 | GCGGGCTCTTTTTTG[C/G]TTCCATATGAACTTT | 10533 |
| rs141482773 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11468661 | CTTGATCCCCCACTA[C/T]TTCATTCTTTCAAGC | 10533 |
| rs141494597 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553010 | CCCATTTGCAGAGGG[C/T]ACTGCTGTTTGGTAC | 10533 |
| rs141505235 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11530954 | CCACTGCACTCCAGC[C/T]TGGGTGACAGAGTGA | 10533 |
| rs141543123 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11305338 | GCAGTTGCTTGAGTT[C/G]TTGGTATGCAGTTTT | 10533 |
| rs141545467 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11432952 | GATGAACCACAGGGT[A/G]TCCAAGTCATGGAGC | 10533 |
| rs141546967 | in-del | -/TTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525031 | CTGTGCAAATCTCAC[-/TTTA]TTTATTTATTTATTT | 10533 |
| rs141562173 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11495061 | TGGGTGACAGAGCAA[A/G]AGCAAGGCTCCGTCT | 10533 |
| rs141562685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348785 | ACAGGGTGCTGATTG[A/G]TCAGTTTTACAGAGT | 10533 |
| rs141565398 | snp | A/G | 1.65239e-05 | 0.00287431 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347891 | GGGTTGGGGCGTGAG[A/G]CACATCACATTTGTG | 10533 |
| rs141570770 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ATG7 | GRCh38.p7 | 3:11420954 | TAGAGATGGGGTTTC[A/G]CCGTGTTAGCCAGGA | 10533 |
| rs141573844 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11453691 | AAAACAGACAATTCA[C/G]ATTGCATTGTGTGAA | 10533 |
| rs141604575 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11284830 | GCTAGGATTACAAGT[A/G]TGAGCCACTGTGCCT | 10533 |
| rs141610530 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11363602 | ACTATTATTATTAGT[C/T]GCAGTTTTGATGGGG | 10533 |
| rs141634934 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11400763 | ATGGAACTTGCCTGC[A/G]AAGCATGTTCTTATA | 10533 |
| rs141635225 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11510965 | AGCTCTTAAGGTGGC[A/G]CGTCTGGAGTCTGTC | 10533 |
| rs141636109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11477333 | TACAAACTCCTGAAT[C/T]GATAAATACGTTCAG | 10533 |
| rs141650703 | in-del | -/GCGAGGGCT | 0.0711525 | 0.174681 | intron-variant | ATG7 | GRCh38.p7 | 3:11513767 | AGGCGCTGAGAGTGA[-/GCGAGGGCT]GCGAGGGCTGCGAGG | 10533 |
| rs141655207 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300035 | GTTCAAGCTTTTCTC[A/G]TGCCTTAGCCTCCCA | 10533 |
| rs141655516 | snp | A/C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11305008 | TACTCTCCATCCCCC[A/C/T]TCCTCCATACTCACC | 10533 |
| rs141656935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509747 | ACTTTTCAGGAACCT[A/G]TCTATTTCTGTAAAG | 10533 |
| rs141702021 | in-del | -/GT | 0.0704125 | 0.17392 | intron-variant | ATG7 | GRCh38.p7 | 3:11290563 | AGCTGTCACTGCCTG[-/GT]ACTTCCAGCCAACCT | 10533 |
| rs141707577 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451974 | GTTCAGAATAGACAA[A/T]CCATAGAAACATAAA | 10533 |
| rs141713010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320986 | ACACATGGTTACTGG[C/T]GTGACAGGAGACAGA | 10533 |
| rs141721827 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11357839 | ACATAGTGAGACCTA[C/T]CTCTACTAAAAATTA | 10533 |
| rs141742243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11277314 | AGGCTCTTCATGATA[C/T]GGCCTTTGCCTGCTT | 10533 |
| rs141744787 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11471891 | TATAGGCGTGTGTCA[C/G]CATGCACAGCTAGTT | 10533 |
| rs141753227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11363130 | TGGCCACATTTCTGC[A/G]TCTTTCCGGACAAAG | 10533 |
| rs141784536 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273652 | AATAAATATTTGTTG[A/G]ATGAATGAATAAAAC | 10533 |
| rs141784643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11325335 | TGTTACTATTTGTTA[A/G]GCGCTGGCCTCATTC | 10533 |
| rs141803606 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11395617 | AAAGAAACGCATCCC[A/G]CAATTTTAAACCCAG | 10533 |
| rs141814171 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526627 | CCTATCTTGTTAGTT[G/T]TAACAGTTTGAAAAT | 10533 |
| rs141831008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11359550 | AAAAACAAAAAATTA[A/G]CTAGGTGTGGTGATG | 10533 |
| rs141844869 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11389059 | TCAAGACCAGCCTGG[C/T]CAACATGGCGAAACC | 10533 |
| rs141850052 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11436208 | ATAATCACATGATAG[C/T]ATAATCAAATAAGAT | 10533 |
| rs141850108 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11476356 | GTGTTAGCTCAATGC[C/T]GTGGATGCGTCAACA | 10533 |
| rs141867212 | snp | A/T | 0.190833 | 0.242898 | intron-variant | ATG7 | GRCh38.p7 | 3:11490145 | CTCAGGACTTGCTTT[A/T]TGAATCTAGGTGCTC | 10533 |
| rs141875569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320031 | CTAAATTCTTTAATA[C/T]GGCCTACAAGAGTCT | 10533 |
| rs141885609 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11315661 | ACCCCTACAGTTATC[A/G]AATCAGCTCCTCTAG | 10533 |
| rs141888882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472339 | GCTTACGTCCCCAAG[C/T]TTAGTGACTCCTGTG | 10533 |
| rs141890174 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11498608 | GATTAAAGCTTCTAA[C/T]GCCTCAGCTGGTGCT | 10533 |
| rs141890557 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11417108 | AGAATGTTCTACCTT[C/G]GTGAATATTCCATGT | 10533 |
| rs141894591 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11534380 | ATGATGGGCGTCGCC[C/T]CAGAATGCTGTTGGT | 10533 |
| rs141907546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434849 | AGCAAAGACAGCTAA[C/T]ATTAGGAAACAGAAC | 10533 |
| rs141913304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11522381 | TTCCTTTCTGCTAAC[C/T]ATAGGTGGGTTTACA | 10533 |
| rs141934745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11456591 | AACCCATGGTGTTTC[A/G]CTTAACACTAATACA | 10533 |
| rs141945213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373266 | TTTATAAAGCCTTTT[A/G]ATTTAAATGTTAATT | 10533 |
| rs141954181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11449926 | AGCCCTGGAGTTGAA[A/G]TAAATTCAACAGCAT | 10533 |
| rs141969744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452509 | CATGCTACGTGAATT[A/T]TATCTCAATAAAGCT | 10533 |
| rs141973805 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | ATG7 | GRCh38.p7 | 3:11511964 | TGCAGCCCTGGTTCC[C/T]GCTCGTGCCTCTCCC | 10533 |
| rs141975412 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11484431 | AAAAACCACAAAAAC[A/G]ACAAACCCAAAAGGG | 10533 |
| rs141976127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550752 | TTATGGTATGTTGTT[A/C]TGTTTTCTCTCAGTT | 10533 |
| rs141978271 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11545029 | GCAGACCCAGCGGAG[C/T]CAGCTGTGTGGGAGG | 10533 |
| rs141998233 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11517209 | AGTTGGGGATGGTAG[C/T]GCATGCCTGTAATCC | 10533 |
| rs142000826 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11310249 | CATTTTACTTCTTTA[A/G]AATAAGTTCTTTGGA | 10533 |
| rs142015855 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11546662 | TCCTTTCAAACTCGT[C/G]TGTCTCCTTTGGAGA | 10533 |
| rs142065270 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272302 | GGTGCTAGGGGCGCA[G/T]TTCCCCGGCATGCCT | 10533 |
| rs142112357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11318839 | TCTGTCACCTGGCTG[C/T]TGCCTCACCTACCTT | 10533 |
| rs142117376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523864 | AGGGATGGGGAAAGC[A/G]GACCTGGACTGGACA | 10533 |
| rs142126094 | in-del | -/AAAGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339321 | AAAAAAAAGAAAAGA[-/AAAGA]AAACCAGCGTATAAT | 10533 |
| rs142127162 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299043 | CTCTTGTTGTGGGGA[A/T]AAAGAAAGAGAGTAG | 10533 |
| rs142130711 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11437802 | AAGTTTTATATACAG[C/T]GGCACCTCACCCCTA | 10533 |
| rs142150650 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11457753 | AGGATTGCTGAGGCC[A/T]GTTAATAAATAAATT | 10533 |
| rs142152764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11335855 | GTCGCGTGCCACCAC[A/G]CCTTGCTAAGTTTTT | 10533 |
| rs142156109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11451954 | AGATTCTATTTTTGT[C/G]AAGTGTTCAGAATAG | 10533 |
| rs142167613 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11346994 | TGAAATAAGAGAGAG[A/C/G]AGAATCTTAGCCTTG | 10533 |
| rs142186782 | in-del | -/GTT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11382025 | CAGAGTCATGTCATA[-/GTT]GTTGTTTCAAAAGAT | 10533 |
| rs142194255 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | ATG7 | GRCh38.p7 | 3:11463158 | CCAAAGTGCTGGGAT[G/T]ACAGGCGTGAGCCAC | 10533 |
| rs142202028 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11485447 | TGGACATTAGCCCTT[C/T]GTCAGATGAGTAGGT | 10533 |
| rs142203763 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11546025 | TGCCTGTAGTCCCAA[A/C]TACTAAGGAGGCTGA | 10533 |
| rs142213811 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11341981 | CTGGGTGGGAAGCTT[C/T]CTCCTCCCTGCTTAC | 10533 |
| rs142214257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11292404 | AGCTGGGATTACAGG[C/T]GTGCACCACCACACC | 10533 |
| rs142216020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413077 | TTTTTGTAGACTGTA[A/G]GGTTTTGTACATGTA | 10533 |
| rs142220561 | snp | A/G/T | 0.000911652 | 0.0213309 | synonymous-codon, missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333077 | AGTGAAGCTTCCAGA[A/G/T]ATGGCATTTAGCCCA | 10533 |
| rs142240102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494147 | TTTAATCAGGCGCTG[A/C]AGCAGGCAAGATGGG | 10533 |
| rs142242547 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11376940 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10533 |
| rs142255121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11337539 | TTATAGGTATAGATT[A/G]TATGGATGCAGGTAT | 10533 |
| rs142258512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297632 | GAAATAATAAAATAT[A/G]TATCATGGCACAAAA | 10533 |
| rs142258801 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11407985 | ACTTAAGCAAACTTC[A/T]GCAGCTGGCTTGAAT | 10533 |
| rs142261383 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11507146 | AATTAGCCAGGTGAG[A/G]TGGCACGCACCTGTA | 10533 |
| rs142279217 | snp | A/G | 0.000292954 | 0.0120992 | intron-variant | ATG7 | GRCh38.p7 | 3:11340765 | CTGTTTTCTCCAGTC[A/G]GGCTTTTTGTAACCA | 10533 |
| rs142279822 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11489177 | TTCTTCTAGATTTTC[C/T]CAGCTGTATGCTGGG | 10533 |
| rs142283520 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446599 | ATGAGCCTTTAAAAG[A/T]ATGAGGCACATGATA | 10533 |
| rs142301064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11514988 | TGGGATTACAGGTGC[A/G]CACCACCACACCCAG | 10533 |
| rs142313134 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422679 | TGCAAGAGGTTTAGC[-/T]TTTTTTTTAGCATGT | 10533 |
| rs142314909 | in-del | -/T | 0.0429648 | 0.14013 | intron-variant | ATG7 | GRCh38.p7 | 3:11300312 | TGTGATTTTTCTCTC[-/T]TTTTTTCAGATGAGG | 10533 |
| rs142326077 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11470490 | CTCATATGTGCAGTC[C/T]ATTGTTGACCGAAAC | 10533 |
| rs142329439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537184 | CCCTCCACTCCTGGA[C/T]GGGCTGGCTCCTTCC | 10533 |
| rs142344472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389751 | CCTCCCACGAGGACT[A/G]CTGTGGAGCATGTGT | 10533 |
| rs142347155 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11468239 | ATTTTTACCATTTGG[A/G]TTTTGGTACCAATCA | 10533 |
| rs142393375 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11502192 | AAAGATGGACAAGAA[C/T]GTTAAATTCTTTTTT | 10533 |
| rs142414463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534742 | TCCCAGCGCAGCCTG[A/G]TAGGCCTCTTGACCA | 10533 |
| rs142426639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499002 | CTAGAGTCTCAGGAA[G/T]TACTCCACAGAGCCC | 10533 |
| rs142493104 | snp | A/G | 4.99023e-05 | 0.00499486 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362856 | AGTGCACTGTGAGTC[A/G]TCCAGGACTGGCCGT | 10533 |
| rs142497285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319072 | TTTAGTGCAATGCTG[A/G]ACACTTAAGAGACAC | 10533 |
| rs142509835 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11279235 | CATTACTGCATTTAT[G/T]GAGAGAGAGCCAGAG | 10533 |
| rs142553168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276893 | CCTGAGTGCTACCCT[C/G]AAACTCAAACAAGTC | 10533 |
| rs142556510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11355605 | ATGGCCATTGAACAC[A/G]TGAAAATGCTCAACG | 10533 |
| rs142564925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396890 | TTGGAAGAGGTTAAA[C/G]ATAGGAATTAATGCT | 10533 |
| rs142567626 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555654 | GGCTGCCTTCCTGCC[C/T]CAGCCGAGGGAGGGG | 10533 |
| rs142583369 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11394983 | TAGATATTGTACTTA[C/T]TAGACATACACTATG | 10533 |
| rs142583735 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11438298 | TCCCCAATGGTGGAG[G/T]CTTTTAAGGAGGTAG | 10533 |
| rs142583996 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11361075 | ACTCCGTATTGTCTC[C/T]GGTGCTTCTCTTAGT | 10533 |
| rs142585683 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11469920 | TCTTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 10533 |
| rs142602947 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11483012 | ACCCTAGTTACTTGG[G/T]ATTCTCAACGTTTTT | 10533 |
| rs142622471 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11356945 | CAGGTCCTTTCCTGC[C/T]TTGCTTGCCACTCTT | 10533 |
| rs142622815 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11307762 | ATCCCAATCCTGTCT[A/C]ACCGCTGTAATCAAG | 10533 |
| rs142628817 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11407468 | TCTAGAGGACAGTGG[C/T]CCTCTTCTCACAGCT | 10533 |
| rs142629118 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520790 | TTTCTCTTTCTTCAT[G/T]ATGTCAGCATTTAAT | 10533 |
| rs142651582 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11444734 | GGGATCTAATTAAAC[C/T]AAAGAGCTTCTGCAC | 10533 |
| rs142654230 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11514881 | AGTCTCGCTCTGTCA[C/G]CCAGGCTGGAGTGCA | 10533 |
| rs142670044 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11294521 | AGCCACTGAGCCTGG[C/G]CAAATCACCTGTTTT | 10533 |
| rs142674226 | snp | C/T | 6.63515e-05 | 0.00575946 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358588 | CCGGTGGCTTCCTGC[C/T]GTCATTGCTGCAAGC | 10533 |
| rs142703237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11369196 | ATACTTATCTCAGTG[C/T]GCTCCTAGGGACATG | 10533 |
| rs142724627 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11467088 | GACATCATGCCATTG[C/T]ACTTCAGCCTGGGCA | 10533 |
| rs142738858 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11551995 | CTCAAGTGATCCACC[C/T]GCCTTGGCCTCCCGA | 10533 |
| rs142742600 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ATG7 | GRCh38.p7 | 3:11513727 | GGGCCCCTCAAGTGC[C/T]GCCAAAGTGGGAGCC | 10533 |
| rs142749866 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11480568 | GTATGAGACCCTGTT[G/T]CAAGAAACAGACAAA | 10533 |
| rs142767171 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11401378 | AATATCTTTGGTTTG[A/G]CTTATGTCAGTCAAG | 10533 |
| rs142769645 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11477786 | ACTGGGAATCAGTAC[A/G]GCCTAGACGCATTCT | 10533 |
| rs142774898 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11478795 | TAGCAAATAAGACAA[C/T]TGAATGTGCAAGCCC | 10533 |
| rs142783523 | in-del | -/T | 0.0592355 | 0.161582 | intron-variant | ATG7 | GRCh38.p7 | 3:11354239 | AAAGCTATGATAAAA[-/T]TTACATGAAAAGAAG | 10533 |
| rs142800905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11377041 | ACCGCGCCCGGCCTT[A/G]TCTGCCGCCTTTTGT | 10533 |
| rs142827864 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11548755 | GATGTGCATCAAATG[G/T]TTTAGTCAGCTGGTT | 10533 |
| rs142866602 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11283793 | AAATATTAGCTGGGC[A/G]TGGTGGCGCATGCCT | 10533 |
| rs142904525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332084 | CACATATACAAGAAT[A/G]TTTACAGAAGCATTA | 10533 |
| rs142911793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11301100 | GGTTGTCAGAGGAAA[A/C]CCAGAAAAGTGTTAG | 10533 |
| rs142950852 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11315066 | AGAATGTTTCGTTAC[C/T]GCTCTAAAACTCTGA | 10533 |
| rs142963098 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | ATG7 | GRCh38.p7 | 3:11490214 | TGTTGTTGAATTGAT[C/T]CCTTTACAATTATGT | 10533 |
| rs142970124 | snp | C/G/T | 0.0162398 | 0.0886349 | intron-variant | ATG7 | GRCh38.p7 | 3:11414563 | GTCTTATTTCATTAG[C/G/T]TAGGCCTTCTATTAT | 10533 |
| rs142973138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11385903 | GTCTTTGTGAGTGCC[A/G]TTTTAATTTTGGCCA | 10533 |
| rs142974892 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11325352 | CGCTGGCCTCATTCT[C/T]AGTTTCTGTGCTAAG | 10533 |
| rs142994648 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365467 | TCATTTTCATTACTA[C/T]ATTTTTGGGAGATTG | 10533 |
| rs142997911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11442928 | CTTGGCTGTACAACA[A/G]ACAAAACAAAAGGAA | 10533 |
| rs142999459 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11344514 | TAAACCCTATTTGTA[C/T]GTGGTATCTTATTCT | 10533 |
| rs143012827 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ATG7 | GRCh38.p7 | 3:11382889 | ATCCATTGTTAACAT[C/T]TTGCCCCACGTATAT | 10533 |
| rs143018424 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11480143 | TCACTGTGTTAGCCA[A/G]CATGGTCTCGATCTC | 10533 |
| rs143025034 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | ATG7 | GRCh38.p7 | 3:11540975 | TGCAATCTTGGCTCA[C/G]TGCAAGCTCCGCCTC | 10533 |
| rs143030877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304529 | GGGCATGTGAAGCTG[G/T]GTGCGAAGTAGATTC | 10533 |
| rs143034218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378339 | TAAAATGTCTTTATC[A/G]ATATGCTATGTGTTT | 10533 |
| rs143035539 | in-del | -/C/G/T | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11391965 | TACTTATTGGGGGGG[-/C/G/T]GGGTAATTTCACTTT | 10533 |
| rs143045900 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11310826 | TTTAGTAGAGAGGGG[A/G]TTTCACCGTGTTAGC | 10533 |
| rs143058378 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ATG7 | GRCh38.p7 | 3:11461450 | AAGAGAAATCAAAAG[A/G]CTTTCACTTTTCCCC | 10533 |
| rs143059607 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11419469 | TAAGGCAGGAGAATT[A/G]CTTGAACCCAGGAGG | 10533 |
| rs143063225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493409 | GTAGTTTTGCAAAAG[G/T]CAACATTCAATTGGT | 10533 |
| rs143084842 | snp | A/G | 0.000280419 | 0.0118377 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313341 | ACTATTGGTTTTGCT[A/G]TCCTGCCCTCTGTCT | 10533 |
| rs143098596 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11458531 | GCATCCCAAAGTGCC[A/G]GGATTACAGGCATGA | 10533 |
| rs143125948 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11536623 | AAACGTTTGTGTGAG[C/T]GCACTCTGGCGGGGA | 10533 |
| rs143128937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11308219 | TAGGGAATGATTCTT[A/G]TTAGTGCAACTGTTT | 10533 |
| rs143131717 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11354478 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10533 |
| rs143138757 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11422816 | GGAGTGCAGTGTGGC[A/G]CAATCTCAGCTCACT | 10533 |
| rs143152453 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11492021 | GGCTGCTTTGTTTAC[C/G]TAAGCAAGCCTTGGC | 10533 |
| rs143153751 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11528585 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGGCAGG | 10533 |
| rs143165726 | in-del | -/T | 0.0547245 | 0.156101 | intron-variant | ATG7 | GRCh38.p7 | 3:11289867 | CCACTGCACTGGGCC[-/T]TTTTTTTCTCTCTCT | 10533 |
| rs143172160 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11352095 | ATATGAGTGAGAACA[C/T]GCGGTGTTTGGTTTT | 10533 |
| rs143175266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369646 | GGTATAGGTCTAACA[A/G]TGTCTGGGCTTCCTC | 10533 |
| rs143208752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11444937 | AGACATACATGTGGC[A/G]AAAAAGCATATGTTA | 10533 |
| rs143209981 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11368701 | CAGTATCACACTACT[A/G]CATTCCAGCCTGGGT | 10533 |
| rs143229841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11467417 | AGTCTCCCTGTGTCG[C/T]CCAGGCTGCAGTGCA | 10533 |
| rs143236771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481368 | AGGGTTCTTACACTT[C/T]TTTAAAGTCAAGGTG | 10533 |
| rs143277503 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11482674 | CCTTGTATATCTTAT[-/A]AAACATCTGAGTGAT | 10533 |
| rs143289860 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11499453 | TTGCTTTCCTTGAAA[A/C]TCTAAAATACGGCCA | 10533 |
| rs143294564 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11309044 | CTCCTCAACAAGTTC[C/T]TCCTCTTGACATTTG | 10533 |
| rs143307991 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11333272 | CTGCTATTCAGACTG[G/T]AACAAAGGCAAAGAT | 10533 |
| rs143314228 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11440253 | TGTAGATGAACTTGC[A/G]ACTCCAATCCCAACT | 10533 |
| rs143333967 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270437 | GCTTCTTTCCTTTCC[C/G]CAGGCTCCTTACTTT | 10533 |
| rs143354435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348566 | CTGACTTTAAGAATG[A/C]AGCCACGGACGTTCG | 10533 |
| rs143374061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11385580 | ACTCATAAGCCAATA[A/G]TGATCTGTTCAGTTG | 10533 |
| rs143376208 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11465495 | CACATCTGTAATCTC[A/G]ACACTTTGGGAGGCC | 10533 |
| rs143390505 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11404180 | CTCTGTCGCCCAGAC[C/T]GGAGTGCAGTGGTGC | 10533 |
| rs143391922 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11282685 | CATCTTCCGGTAGAG[C/G]CTACTCTTTCTTCTA | 10533 |
| rs143396792 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ATG7 | GRCh38.p7 | 3:11495020 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 10533 |
| rs143439724 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11509565 | CTTTTAAGTAAGTGA[C/T]GTTTTAGAGTTTGCT | 10533 |
| rs143456128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413520 | ACTTGGTCATGTTGT[A/G]TAATCCTTTTAATAT | 10533 |
| rs143456329 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11342814 | AACATTCTTATACTT[C/G]TATGTTTATATATCC | 10533 |
| rs143459085 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11544182 | AGTAGGCAGGGCTAA[C/T]TCTGAGTTGCCCCAG | 10533 |
| rs143463031 | snp | C/T | 0.0111284 | 0.0737589 | intron-variant | ATG7 | GRCh38.p7 | 3:11330826 | TTTCCAGATGAAGAT[C/T]GGGATTGGAGTGGGA | 10533 |
| rs143465499 | in-del | -/CCCATT | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11524283 | GCCACAATGGAGAAG[-/CCCATT]CCCACTCTTGTCCCC | 10533 |
| rs143520419 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11430058 | TGTTACTTTCCTGCC[C/G]AGAGATATTCTTTAG | 10533 |
| rs143533215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11291847 | TGGTAGAGAGGGGAA[A/G]GGTTTCCTAGGAACA | 10533 |
| rs143545741 | snp | C/T | 0.00217461 | 0.0329026 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11348028 | TCCAGAAAATATTCC[C/T]CGGTGTGGTATGTTG | 10533 |
| rs143564021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11445840 | TTAAAATTTTTGCCA[A/G]TCTGTATAACAGTAT | 10533 |
| rs143571596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11544466 | GCAAGAAGTACCCAC[C/T]GCTGTGTGTCCCTGT | 10533 |
| rs143602986 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11291434 | TATAGTGACGAGAAC[A/G]GGGGCTTTGAAGCTA | 10533 |
| rs143611090 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11371506 | GACTGGAGGTGATAC[A/G]AGTGGCTCTGGGAAT | 10533 |
| rs143619900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11299759 | TCCTTTAGTCCATGG[A/G]CATTGTCCATGGGCA | 10533 |
| rs143628966 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400550 | CCTTCGAAGAGTAGA[C/T]AGAAATGTGAATTTT | 10533 |
| rs143649914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482290 | CTGGTGTTTGGGCTC[C/T]GAGCTCTTTCAAGAA | 10533 |
| rs143654799 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11493688 | TAAAACACAGCAGGC[A/G]CAAGGTAGGTAAATA | 10533 |
| rs143678037 | in-del | -/TC | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11409586 | ATAAGTTGATGAGCA[-/TC]TGTTTTTCTTTCATA | 10533 |
| rs143688926 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11357657 | ATGGAGATGTTTAAC[A/G]CTGAGGAAACAGAAG | 10533 |
| rs143709344 | in-del | -/TTA | 0.283421 | 0.247756 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286910 | GCACCCAACCTTTTT[-/TTA]TTATTATTATTATTT | 10533 |
| rs143719167 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558049 | CACATAAAGTTGTCA[C/G]GCAACTTTAGTCCTC | 10533 |
| rs143724311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11371958 | GCTGTCCAGCTGGGA[A/G]CAGCCCGGGAGCGAG | 10533 |
| rs143747842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289314 | AAATTCCCCTCCGAC[C/T]ATTACTTCTTAAATC | 10533 |
| rs143748911 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11479061 | TTACTTTGTGGATAC[G/T]GGCCACCACTTGAAG | 10533 |
| rs143760575 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11484337 | AGGCGGAGGCTGCAG[C/T]GAGCCAAAATCATGC | 10533 |
| rs143780546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516558 | TGTGTGATCCAGCAA[C/T]TGCACTCCTTGAGAT | 10533 |
| rs143782215 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527301 | GCAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 10533 |
| rs143794261 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11274492 | AAGAGTGGTTCGAAG[C/T]GAGATGAGCAAAGGG | 10533 |
| rs143796439 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11426642 | GAAAAGATGATAAAT[A/T]CTAAGCCGTACTAGT | 10533 |
| rs143804461 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11352716 | TTATAATTGAAATAC[A/T]AAATGCTAAAAGGGA | 10533 |
| rs143820473 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11527934 | TTGCCCGTATCCATG[C/G]AGAAATGCAGGAGTG | 10533 |
| rs143840548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349565 | AATAATAATAAATAA[C/T]CCATCTCACATATTC | 10533 |
| rs143884129 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270659 | AAAAGCAATGTTTTG[C/G]GGGTAGGGGGTGGAT | 10533 |
| rs143911108 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11387030 | AATTGCAATGGCTGA[C/T]GTGTATCCAGTTCCC | 10533 |
| rs143911849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466334 | GTAAGGTGAGAAAAT[C/T]CTTCAGCAAATTCTA | 10533 |
| rs143930165 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11383331 | TTTCCCTCCATGTGG[A/G]TTTGTCTGATGTTTC | 10533 |
| rs143930826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11495236 | GGGATTGTCATGGAC[A/C]TTGAAGTATGGACAG | 10533 |
| rs143933316 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11360071 | CTTTTTCAGAGATAG[A/C]ATCTTGCTCTGTCAC | 10533 |
| rs143933515 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11437552 | CTGAATTTTTAAAAT[G/T]TCCCTGTTTACCACA | 10533 |
| rs143934419 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11373828 | TTTATGCAGTTCTTA[C/T]AAGATTGAGGAAGTG | 10533 |
| rs143964044 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11534748 | CGCAGCCTGGTAGGC[C/T]TCTTGACCACCTGGG | 10533 |
| rs143968282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11295901 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT | 10533 |
| rs143989663 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11312061 | GTATGAGATTTCTTT[C/T]TGGAGTGATGAAAAT | 10533 |
| rs143997022 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11437396 | CTCCCCTCTGTGCTT[C/G]CTGTGGGGAGAGAAA | 10533 |
| rs144000773 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11384294 | AACAGCCTGTTGTGA[A/C]GAATCAGGCTCCAAA | 10533 |
| rs144013696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11383361 | CCCTATGATTCGATT[C/G]AGGTTATGAATTTTT | 10533 |
| rs144014701 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510769 | GCAGTCAGACTTCCA[G/T]GCTTGGGGTAGAATC | 10533 |
| rs144015876 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11379457 | ATGTTTTACATTTTA[-/TC]TCTATCTGTTCCAAA | 10533 |
| rs144017462 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11431260 | TACAAAATTAGCTGG[A/G]TGTGGTGGCATGTGC | 10533 |
| rs144020423 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11494274 | GTAAGGAAGAGGAGT[C/T]GGTCAACAGGAAGCA | 10533 |
| rs144058496 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11311413 | GTTTGAGACCAGCTT[A/G]GGCAACATAGTTAAA | 10533 |
| rs144065039 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11493729 | AAAAACAAAAGTTTC[C/T]GTGATACAGCCTAGG | 10533 |
| rs144068444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531276 | AAGTCAAGGAAGAGT[A/C]TGAATGTGAGTGTGG | 10533 |
| rs144068600 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11492574 | TTGTGCTCAACTCCT[C/T]GCGGGAGGGAGCACG | 10533 |
| rs144073041 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11517898 | TGTTTTTAGCAGGGT[A/G]GTGTGATCAGATTCC | 10533 |
| rs144081382 | in-del | -/GCTGTGCTGTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524206 | GGCTCCCCTTCACTA[-/GCTGTGCTGTG]GCTTAGTTAAGCTGA | 10533 |
| rs144091965 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11543076 | GCCACAGTTAGATGG[C/T]GGCGTCCTCCAACCG | 10533 |
| rs144094273 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339314 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAC | 10533 |
| rs144099612 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11326680 | TAGTTGTGTGGCAGA[C/G/T]GCTATCTGTCATGAT | 10533 |
| rs144114810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429901 | CAGTGAGCTGAAATC[A/G]CGCGACTGAATTCCA | 10533 |
| rs144156305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11530254 | CAGAGAGAGCGAGGC[C/T]CTGCAAGCAGTGGCA | 10533 |
| rs144167757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11388302 | GGCCCAGCTGTATCC[A/G]ACTGGGTGATGGAGG | 10533 |
| rs144183677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287556 | AAAGCATAAGGAAAC[C/T]ATCAGAGGTGTAGTC | 10533 |
| rs144184912 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11336372 | CCACACCGTACATTT[A/C]CATTTGAAAAAGGTT | 10533 |
| rs144186331 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554911 | CCATCGCCAGAGCAG[A/G]ACTGCTGACCCCAGG | 10533 |
| rs144203349 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11333173 | TTCTTTTCATATCGT[C/T]ACAATGGCAGAAGAA | 10533 |
| rs144209678 | snp | A/G/T | 0.00716521 | 0.0594565 | intron-variant | ATG7 | GRCh38.p7 | 3:11453986 | ATCAGAGGAAATTCC[A/G/T]TGTAAATAAATGTGA | 10533 |
| rs144226090 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11380721 | CCTTCTGCTGCCCAG[C/T]GACTTGACCTGGGCT | 10533 |
| rs144230099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11458596 | ACAGCCAGCTCAGCT[A/G]TTAACACATTGTGTG | 10533 |
| rs144233748 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11481880 | GGCCAAAGGCCTTTG[A/G]CCTGGCAAGAGTTGT | 10533 |
| rs144236149 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11274638 | CAATAGCATGTTACC[C/T]GCACATAGACTTTGG | 10533 |
| rs144239774 | snp | G/T | 0.02016 | 0.0983543 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451171 | TTTTGAAAAGGACAG[G/T]CTGGAACAAGAACTT | 10533 |
| rs144249468 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ATG7 | GRCh38.p7 | 3:11491858 | AGAGGAGTACCCGGC[C/T]GTGTGAGGTATCAGG | 10533 |
| rs144277505 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11551233 | TTTCATGGCGTCTCC[A/C]TCGGCCCATGGTGGG | 10533 |
| rs144294953 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11545726 | TCTGTTGTCAGCCCC[C/T]CTGGCGGTTCTTCCT | 10533 |
| rs144301641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364441 | TTAAGCAACTTGCCT[A/G]TGGTCACAAGCTCAG | 10533 |
| rs144314388 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11537726 | ATTTCCTGAGGCCCT[C/G]CTCGGTGCCAGGTTC | 10533 |
| rs144329287 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11452960 | TCCGTGGGCTGTAGC[A/G]AGCACAGTAGCAGTC | 10533 |
| rs144337345 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11447461 | AACAGTGCAAGACTC[C/T]GTCTCAGGGAAAAAA | 10533 |
| rs144340340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11360366 | ATGAGTTTCAAATGA[A/G]ATTAAATGAGATAAT | 10533 |
| rs144387308 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11494803 | AACAGGCCAGGCATG[G/T]TGGCTCACACCAGTA | 10533 |
| rs144400612 | in-del | -/AAAC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392464 | GGAAATCATTAAAAA[-/AAAC]AACAAACAAAAAAAA | 10533 |
| rs144415880 | snp | A/C | 0.00243458 | 0.0348046 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11340731 | GAATGTATGGACCCT[A/C]AAAGGTATATTTGGG | 10533 |
| rs144425767 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11417698 | CCATATTTGTAACTA[G/T]TTTCCATTTGTCACC | 10533 |
| rs144476207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394608 | AGCCTGAGAACCCTT[A/G]TAAATCATTCTTGAC | 10533 |
| rs144481586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522688 | AAAATGGTCTACCCA[A/G]AGCTTTCAGTGGGTA | 10533 |
| rs144496598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442019 | TGTTGCCCAGGCTGG[C/T]CTTGAACTCCTGGCC | 10533 |
| rs144504283 | snp | A/G | 0.000199008 | 0.00997319 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342273 | CAATGTAGCTAGGAC[A/G]TTGATGGTAAGTCGG | 10533 |
| rs144518456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335341 | GAAGAAGAATTGTCT[A/T]GGACCACACATAAAA | 10533 |
| rs144535084 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11405823 | TGGGGTTTCGCTGTG[C/T]TTCCCAGGCTGGTCC | 10533 |
| rs144539439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351113 | CCCCCTTCCCACTGT[G/T]TATTTGTTTAGTTGC | 10533 |
| rs144555762 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271018 | GATCAAGCCACCCCT[G/T]CATCCCACTTCCCAT | 10533 |
| rs144558373 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11460037 | AGTCACACAGCTCAG[A/C]ATCCCAACTCTGGGT | 10533 |
| rs144564759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518133 | GATGGGTTGAGGGCG[A/G]GGCAATCAGAGAAAG | 10533 |
| rs144571347 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11549985 | GAGGACTGCAAACTG[C/T]ACGTCTTTTCTTATT | 10533 |
| rs144584927 | in-del | -/TTCTT | 0.0663309 | 0.169604 | intron-variant | ATG7 | GRCh38.p7 | 3:11551741 | AGCCAATATAATGGG[-/TTCTT]TTCTTTTCTTTTTTT | 10533 |
| rs144585307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466955 | ACTAACATGGTGAAA[A/C]CCCATCTCTACAAAT | 10533 |
| rs144586355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387800 | ACGGTGAAACACTGT[C/T]TCTACTAAAAAGGCA | 10533 |
| rs144591388 | in-del | -/TTTT/TTTTG | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11464361 | TGGGTGAACGAGCAA[-/TTTT/TTTTG]GACCCTGTCTCAAAA | 10533 |
| rs144602389 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11284189 | TAAAAAATCCTGTAT[G/T]TCTTCATTAAAAAAT | 10533 |
| rs144625228 | in-del | -/TC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515693 | CTTTCTCTCTCTCTC[-/TC]ATACACATACACATC | 10533 |
| rs144638053 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486223 | TTTATTTCATGAGCA[A/G]TGGTTTGTATTTCTC | 10533 |
| rs144688287 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11346065 | TCTATGAGGCCTTTT[A/T]ATTTTTTGGGACAGG | 10533 |
| rs144693224 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11521318 | GTGTGACTGGGACCG[A/G]CACAGGAAAGGGTGG | 10533 |
| rs144696160 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11307137 | TGTGATCAGGCACAT[C/G]GGTCTGCTGCAGAAA | 10533 |
| rs144702814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385091 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCATT | 10533 |
| rs144702827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343988 | TTTGTTTTTCAGTAG[C/G]ATTTTCTTTATATAG | 10533 |
| rs144717550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462347 | AAGACAAAGTTTATC[A/G]TGGTCACAAGTCCTA | 10533 |
| rs144719381 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11380923 | ATTTCTCTATTCTGA[G/T]TTGACAAGCTTCCTT | 10533 |
| rs144742151 | in-del | -/TTTG/TTTGTTTG | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11385016 | TGCTTAAATAGTGTT[-/TTTG/TTTGTTTG]TTTGTTTGTTTGTTT | 10533 |
| rs144763411 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11476238 | TTGAGAGGGCTTACT[A/G]TGTTGCTGTTAGTTT | 10533 |
| rs144786187 | snp | A/G | 8.27904e-05 | 0.00643338 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313405 | GGGTTTGGATCAAAG[A/G]TTTTCACTAAAACAG | 10533 |
| rs144789183 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11325126 | ACCAGGTAGCCCAGG[C/T]GTGGTGTAGTAGGCT | 10533 |
| rs144797897 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11399857 | GGGATTACACGTGAG[C/T]CACAGTGCCTGGCGT | 10533 |
| rs144803516 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486233 | GAGCAGTGGTTTGTA[G/T]TTCTCCTTGAAGAGG | 10533 |
| rs144827635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11365300 | CTTTATAGGCAGGCA[C/T]GAGAAAAACATTAGA | 10533 |
| rs144847975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442054 | GCCATTCACCTGCTT[C/G]GACTTCACAAAGTTC | 10533 |
| rs144848688 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11478251 | ACTTAAAAAAAATTA[C/T]TTAAATGTTTTCCCA | 10533 |
| rs144855565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508752 | TACCATGCACAGCCC[C/T]ATGTAGCCTATTTTG | 10533 |
| rs144855830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302878 | TATTAGATGAATTGT[C/G]AGTCAAGTAGTATTT | 10533 |
| rs144875981 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11438360 | TTGAAAAGTCAAACA[A/G]GAGTAAAACATTTAG | 10533 |
| rs144886151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478250 | AACTTAAAAAAAATT[A/T]TTTAAATGTTTTCCC | 10533 |
| rs144886738 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11418168 | GGAGTGCAATCGTGC[A/G]ATCTCAGCTCACTGC | 10533 |
| rs144893212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11504918 | GAGTTTGCCATGACA[A/G]GGGTAAGGGGGCTCA | 10533 |
| rs144894309 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11538054 | GGATTCCAGATGACC[C/G]CTGTTGTCCAGCTGG | 10533 |
| rs144906921 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11464653 | TAAATATCCCCCAAA[C/T]GAAAGACAAATACAG | 10533 |
| rs144915299 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11523437 | AGGATTATTGTTAAC[A/T]TTTACCACATGTATG | 10533 |
| rs144918110 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11361076 | CTCCGTATTGTCTCC[A/G]GTGCTTCTCTTAGTC | 10533 |
| rs144930915 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11535447 | GGCCCTCCCTGAGCA[G/T]GTTTGTATGGCAATC | 10533 |
| rs144996259 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11412330 | CAGATAAAACAAATA[A/T]GAGTTTCAAGCTTTA | 10533 |
| rs144998661 | snp | G/T | 0.130694 | 0.219696 | intron-variant | ATG7 | GRCh38.p7 | 3:11485414 | TCTTGTAAATTTGTT[G/T]GAGTTCATTGTAGAT | 10533 |
| rs145032019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11366667 | GGTTTCCTTCTTTAA[A/G]TCCTTTATGTTAAAT | 10533 |
| rs145054529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288065 | TGTTTGAGGCCTGCA[A/G]TGCCTTAAAATATTT | 10533 |
| rs145070961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11362152 | ATCTGCTCATAAGGT[A/G]AAATTTTTATAGAGT | 10533 |
| rs145074081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11283856 | AGAATCGCTTGAACC[C/T]GGTAGACGGAGGTTG | 10533 |
| rs145078554 | snp | A/C | 8.23676e-05 | 0.00641693 | missense, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298727 | GGGATCCTGGACTCT[A/C]TAAACTGCAGTTTGC | 10533 |
| rs145097787 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11420693 | ACTATACTGTAGTCT[A/G]TTAAGTGTGCAATAG | 10533 |
| rs145098823 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11491404 | GTTTTCAACTTCTTT[A/G]CCTTTGGTTTGAATT | 10533 |
| rs145111378 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11327764 | CAAGTTTGAGATCCA[C/T]GGCCATTAGAAGGTT | 10533 |
| rs145144803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11415618 | ATACACATTAGCCTA[C/T]GCCTACTCAGGGTCA | 10533 |
| rs145146479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524679 | GTAGTCCCAGCAGCT[C/T]GGGAGGCTGAGGTGG | 10533 |
| rs145165967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519947 | CCCCACTTGCAGATA[A/G]TGACAGATTTTTTGG | 10533 |
| rs145168762 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451918 | CACACACACACACAC[-/AT]ATATACATATCTCTT | 10533 |
| rs145214602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439364 | GTGAGCCACTGCACC[A/G]GGCCTGAGCTCTTAG | 10533 |
| rs145252780 | snp | C/G | 0.0236965 | 0.106392 | intron-variant | ATG7 | GRCh38.p7 | 3:11374671 | AGCACTTTGGGAGTC[C/G]GAGGCGGGCAGATCG | 10533 |
| rs145254625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11381044 | TAAATTTGGTTACGT[A/T]TAGATGCTCAAAAAT | 10533 |
| rs145257253 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11459674 | TGTGGGGAAAAGGAA[A/G]TATACTGGCACAATT | 10533 |
| rs145275683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11455869 | TCAAAACTTACCTCA[A/G]ATACCTAACCTGTCT | 10533 |
| rs145279032 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11553629 | CCTGGTCACTGGACC[A/G]CAGACCGGCCCATCC | 10533 |
| rs145283409 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298631 | CAAATGTTCTTTCTC[A/G]CCAGGTTTTGCATGG | 10533 |
| rs145293590 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11377958 | CACATTCCTGAGATG[A/T]TAGGAACTAAAAGGT | 10533 |
| rs145299759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11550725 | TCTTTGTCTATTACC[A/G]AGATGAGCCCTTTAT | 10533 |
| rs145305544 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ATG7 | GRCh38.p7 | 3:11381878 | GCTACCTTCTTTATT[C/T]GCTTAGGAGATTGTC | 10533 |
| rs145344572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11309505 | TCTGTAAGCGAAATC[C/T]AATTAAAATGAACGT | 10533 |
| rs145375362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494859 | TGAGTGGATCACGAG[A/G]TCAGGAGTTCGAGAC | 10533 |
| rs145383419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305035 | CACCAGCCCTAGCCA[A/G]CCATAACTCTACTTT | 10533 |
| rs145388950 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11425123 | GCACTCCACCATGCC[C/T]GGCTAATTTTTAAGT | 10533 |
| rs145391406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328468 | GTATTAAATTAAATA[C/T]GAATCTGTCTATTTG | 10533 |
| rs145394796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378920 | GATGGCTAAACGGTG[A/G]TGGATCGGGTCTTCT | 10533 |
| rs145395722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532555 | TGGCAACGTCCTGTC[C/T]GTTCATAAAATTCAA | 10533 |
| rs145413114 | snp | A/G | 0.00175759 | 0.0295923 | intron-variant | ATG7 | GRCh38.p7 | 3:11446467 | TAGGGGAAACTTGGC[A/G]TCATCATTCAAAATA | 10533 |
| rs145416657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535893 | CAGATCCCCTAAAAC[A/G]GGAGCCCCAAAGCTT | 10533 |
| rs145420673 | in-del | -/C | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11454296 | GCAAGGTAGTTGGGA[-/C]CCCAGGCAATCAGCA | 10533 |
| rs145441364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543742 | CCATCTCTACTAAAA[A/T]TACCAAAAAATTAGC | 10533 |
| rs145444053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11346563 | CATTCCAGGAAACCA[A/G]AAGTTAAGTGTGTGC | 10533 |
| rs145456510 | in-del | -/CACA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502041 | TATACACACATACAC[-/CACA]ACATATGTTTATATA | 10533 |
| rs145459226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460117 | GTAGGCAGCCTCAGT[A/G]CTACATGACCAACCA | 10533 |
| rs145461141 | in-del | -/TGA | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11535498 | AGAGCAGGCTCTCTT[-/TGA]TGGATTAGGGGGAGG | 10533 |
| rs145470536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276156 | ATTCATTCCTCTCCT[C/T]AACCTCCTACCTTGA | 10533 |
| rs145477131 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11492492 | TTGGCTCCAGCCCCT[C/G]CAGGATATTTTCTTG | 10533 |
| rs145483162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11341263 | GACAGGGTTTCACTG[C/T]GTTGCCCAGGCTGGA | 10533 |
| rs145484503 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11540309 | GACAACATCTTTCCC[A/G]CATCTCTGATGGGGA | 10533 |
| rs145484725 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555270 | GCTGCCCACCGCACC[A/G]CAGGCTCCTCCTGTG | 10533 |
| rs145488856 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11324455 | TTTTGTCATTTTCCT[A/G]TTCGACGCCTGCCTT | 10533 |
| rs145523115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440614 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTTTACT | 10533 |
| rs145526150 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282193 | GTCCCTCCCATGTAG[A/G]CTTCTCAAACCCCAT | 10533 |
| rs145539203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11514761 | CTGGCACAGCACAGT[A/G]CTAACCACAAGGAGA | 10533 |
| rs145563586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476532 | CTCCTCCCAGAGATA[A/G]AGTCCTGGCCTGAAA | 10533 |
| rs145565067 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11455588 | GTGAGAACAACTGAT[C/T]GTGAGCTTGTCCATG | 10533 |
| rs145570694 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11536712 | CCGACCCTGCGGCTC[C/T]GACCGGGGCCGAGCA | 10533 |
| rs145573600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398808 | GTGAGCTCTGATCAT[G/T]CCACTGCACTCCAGT | 10533 |
| rs145575744 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11473922 | ACGTTCAAACCTCAG[G/T]TCCCCTGCTTTGTAG | 10533 |
| rs145612843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11395650 | GATAATACCGTTCAA[A/G]AATGAAAGGGCTGGG | 10533 |
| rs145616556 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11505611 | GCAAAAGAGTCTTCT[A/G]AAGACCACTCTCAGC | 10533 |
| rs145616987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470380 | TGAGTGTACTGAACA[C/T]TGTGGGCAACTGGAA | 10533 |
| rs145621215 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ATG7 | GRCh38.p7 | 3:11371381 | GGCACAGCGGAGAAG[A/G]CAGGAATGCAGGGGC | 10533 |
| rs145638654 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11283489 | AAATCCAGGTGCAGG[A/G]GGGTGAAGGAACCTG | 10533 |
| rs145640300 | in-del | -/TG/TGTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366971 | ATATATGGGAAAAGC[-/TG/TGTG]TGTGTGTGTGTGTGT | 10533 |
| rs145665885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11399613 | ACAGTCTCACTCTAT[C/T]GCCCAGGCTAGAGTG | 10533 |
| rs145685033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11278716 | GGTGCTAAGTCAGGT[A/G]CTAGAAAAACAATGA | 10533 |
| rs145708354 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11502979 | CAGAGTTGAAAGTAG[C/T]GTGTATACCACTGAA | 10533 |
| rs145719245 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11326164 | CCTGCTTACTGTTAA[A/G]CAAGTGAGTTTTTCA | 10533 |
| rs145737109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11291596 | AACATGTAAACTGTT[C/T]AGTGTAGTGCTTGGT | 10533 |
| rs145745107 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11404328 | TTTAGTAGAGATGGC[A/G]TTTCACCATATTGGC | 10533 |
| rs145745233 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11456632 | CCTAGGAAATATAAA[C/G]CCTTGAGAGCTGAAA | 10533 |
| rs145751108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11515031 | TTTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 10533 |
| rs145767782 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11407275 | TCCGTGTCTCACATC[C/G]AGGTCATGCTGATGC | 10533 |
| rs145772101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11503822 | TAAATATATAAGTTT[A/G]AAATTCAGTAGAAGG | 10533 |
| rs145772371 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11461334 | AATGGCATCACTGGG[G/T]CTAAGAAACCAAAGA | 10533 |
| rs145781933 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 3:11335022 | ACAGTCAGAAGGATT[C/T]AGGATTGGCCCACAT | 10533 |
| rs145784130 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 3:11336964 | AGGTGTGAGCTACCT[C/T]GCGCAGTCGAGGAGT | 10533 |
| rs145810785 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11352304 | GTGAATAGTGCCGCA[A/G]TAAACATATGTGTGC | 10533 |
| rs145814321 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11382400 | TGGAACATTTATCCA[G/T]AAATCATTTCTTATC | 10533 |
| rs145825578 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11556043 | GCCCACCCAGCCTGG[C/T]GCTGAAACTGCACAC | 10533 |
| rs145827275 | in-del | -/G | 0.0364509 | 0.129988 | intron-variant | ATG7 | GRCh38.p7 | 3:11531217 | GGCAGTCTAGAAGAA[-/G]GGGGGGGCTGTGCAG | 10533 |
| rs145832684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467656 | GCTGGGATTACAGGC[A/G]TGAGCCAATGCGCCT | 10533 |
| rs145837418 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11452782 | GATGGCACTTTTCTT[C/G]ATAGGAGATAATTAT | 10533 |
| rs145840041 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286830 | GGCTGGTCTCAAACT[C/T]CTGAGCTCAAGCTAT | 10533 |
| rs145851510 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11365310 | AGGCATGAGAAAAAC[A/C]TTAGAAGCATGCAGG | 10533 |
| rs145862856 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11458086 | ACATTGATTTTTATG[C/G]AACTAGTGTCTTGTT | 10533 |
| rs145863195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492756 | AAACTCTTGTTTGCT[C/T]AGGCCCATCGCACTC | 10533 |
| rs145866721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402605 | ATATCACACATGCAC[C/T]AGCCCCGTGAAAGTC | 10533 |
| rs145878050 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11498541 | TAATCTTCCAAAAAC[A/T]TTGGTTTTCACCGTG | 10533 |
| rs145882599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11546865 | GTCAGGCTGACCAGA[A/G]GGGCTGAGCCCACCC | 10533 |
| rs145886284 | in-del | -/GGCCAGGGAAAGGTGGAGGGAAGAGGGCATAGGTCCCAGTGT | 0.138886 | 0.22395 | intron-variant | ATG7 | GRCh38.p7 | 3:11537996 | CCTGAATGTAGAAGA[lengthTooLong]GGGATTCCAGATGAC | 10533 |
| rs145939018 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11500616 | TGAGTATAGATAATA[C/T]AGTGCTTAGGAAAAT | 10533 |
| rs145939469 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11467240 | CAGTGGTTAGTAACA[A/C]CTCTGGAGTCAGACC | 10533 |
| rs145941406 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273780 | TAATAGTGGTGGTGG[G/T]GGCGGTGGCGGCATT | 10533 |
| rs145950152 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11497429 | TGCCTGTAATACCAG[A/C]TACTCAGGAGGCAGG | 10533 |
| rs145962843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299078 | ACTCAAATTATTAAT[C/T]CAAATAATACCCATT | 10533 |
| rs145976533 | in-del | -/A | 0.0283406 | 0.115616 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556763 | CGTAACGATGGTCTC[-/A]AAAATCACCCATATA | 10533 |
| rs145987804 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11546356 | TTTGTATTTTTAGTA[A/G]AGAGGGGGTTTTGCC | 10533 |
| rs146004739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358896 | CAAGAGGACAGAGAC[G/T]TGGTCTTATTCACCA | 10533 |
| rs146005393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11279500 | ACCAACCTGACCAAC[A/G]TAGTGAAACCTTGTC | 10533 |
| rs146006185 | snp | A/G | 8.45988e-05 | 0.00650325 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358611 | CTGCAAGCAAGAGAA[A/G]GGTAGGCCCTGTCTC | 10533 |
| rs146016800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11353661 | CGACCTCTTAGTTCA[C/T]GTGAGCGAGAGCTAG | 10533 |
| rs146017307 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11396907 | TAGGAATTAATGCTT[C/G]ACTGAGATAAGTCAA | 10533 |
| rs146034089 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469310 | CAAAATTAGCCAGGC[A/G]TAGTGGCGCATGCCT | 10533 |
| rs146043998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393145 | AAAGTGTTAGGCTGC[C/G]TGGTTTGCCAGATTC | 10533 |
| rs146054644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405904 | GATTATAGGCATGAT[A/G]CCTGTAATCCCACTG | 10533 |
| rs146059918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516995 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACCTGGG | 10533 |
| rs146070500 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11552041 | GGCGTGCGCCACCAC[A/G]CCCGGCCTCTTTCAT | 10533 |
| rs146073140 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11513949 | CCACTATGCAGTCTT[C/G]ATCTCCCACGCTCAA | 10533 |
| rs146082798 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11454371 | ATGACCCAATCTTAA[C/T]CAATGAGGTATGATG | 10533 |
| rs146097710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548913 | GTCAAAAGTTAAGCC[A/G]TAGGAATCGTGGCTG | 10533 |
| rs146129542 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11301224 | TTAAGTCATTGTGGT[C/T]CTTAAGAATTCAGTT | 10533 |
| rs146141922 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11297153 | ACAAATCCAAGAGCT[C/T]GAGACCAGCCTGGGT | 10533 |
| rs146155216 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11410445 | TATGTGATAGAATAC[A/T]TATAAAATTTGCCAT | 10533 |
| rs146180540 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11472350 | CAAGCTTAGTGACTC[C/G]TGTGGAAGGAGAGCG | 10533 |
| rs146180577 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11431127 | CCATTTTGGCTGGGC[A/G]CAGTGGCTCACGCCT | 10533 |
| rs146181588 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534453 | TCACAGGCAGGTCCT[A/G/T]TGTTGCCCTGTGGGT | 10533 |
| rs146191319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11469535 | CTGTGACAAAATGTT[C/T]ATCTCCATACTCTTA | 10533 |
| rs146192336 | snp | A/G/T | 0.0127154 | 0.0788808 | intron-variant | ATG7 | GRCh38.p7 | 3:11531223 | TCTAGAAGAAGGGGG[A/G/T]GCTGTGCAGGGTACC | 10533 |
| rs146214111 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11337729 | TAAATCCTTCCTCCT[C/G]CAATCTTTCCTCCTG | 10533 |
| rs146228476 | in-del | -/AC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309686 | TGCGCGTGTGTGCGT[-/AC]ACACACACACAGATA | 10533 |
| rs146243378 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ATG7 | GRCh38.p7 | 3:11408342 | AGCATTTTTGTCAAA[A/G]CCATTCAGCAAGTCT | 10533 |
| rs146246974 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11321405 | ACAGCTGGGACTGCC[A/G]TGGTCTCAGTTTTGA | 10533 |
| rs146258438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11363206 | TTTGTGCTAGGCACT[C/G]TTCTAAGCACCTTAG | 10533 |
| rs146274355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436700 | TGGATAAAATGTCAG[C/T]TATTACGCTGGAATA | 10533 |
| rs146284388 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11359731 | AAAAAACAAAAAAAA[A/C]CCAACTATGCGGAGC | 10533 |
| rs146288670 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11548596 | TTGCAAAATTAAAAA[A/C]CTTTTTTTCTTAAAC | 10533 |
| rs146299050 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450651 | CAGATCTGCTCTTCT[C/G]AGGGACCATCTTGCC | 10533 |
| rs146310376 | snp | A/G | 0.214843 | 0.247516 | intron-variant | ATG7 | GRCh38.p7 | 3:11484978 | TTCCAAGTCTTTGCT[A/G]TTGTGAATAGTGCCG | 10533 |
| rs146322874 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11427636 | GCCTGGCCAACATAG[C/T]GAAACCGTGTCTTCA | 10533 |
| rs146353186 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11533245 | CTCCAGCTCCCTTTC[A/G]TCATCACCGTGAGTG | 10533 |
| rs146369101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339520 | AGCAGTGGGAATTCA[A/G]TGAGAAAGGGGGAGT | 10533 |
| rs146379794 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11335887 | TATCTTTAGTAGAGT[C/T]GGGGTTTCACTGTGT | 10533 |
| rs146380057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11379833 | GGAAAATACTCATTT[C/T]GAACTTATTTTTGCT | 10533 |
| rs146391798 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11352870 | GGTCTTGAGGAGGGA[A/G]GCAAGGACCAGAGAG | 10533 |
| rs146393955 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11453787 | ACTTCTAAGGCCTGA[G/T]CAAACCCTCAGTGAT | 10533 |
| rs146405109 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11376984 | GACCTCATCATCCGC[C/G]CTCCTCGGCCTCCCA | 10533 |
| rs146416341 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11388495 | GTGCAGTGGCGCTAT[C/T]TCAGCTCACTGCAAG | 10533 |
| rs146427023 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11528364 | ACCTTCAGAGGAATC[A/G]CAGTCAGTCACTTAC | 10533 |
| rs146454570 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11382061 | GGCTAAAAATTACTT[A/T]TAAAAATTTATCCTT | 10533 |
| rs146458085 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11494624 | GCAAAGTCCTTTTTC[A/T]TCACTTTAAGCTGTT | 10533 |
| rs146473773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468500 | GCTGCTGGGACTTAG[A/G]CACTGGGCCACTGAG | 10533 |
| rs146474260 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11545892 | ATTGTTTCCCGGAGG[C/T]ATTTTGGGAGGCCAA | 10533 |
| rs146474973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508618 | CCTGCTAATATTATT[A/G]TTATTTTCTTGTAAT | 10533 |
| rs146484426 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11447514 | TAATGAAACCAGGTC[A/G]TGAAATCTGGGCTTC | 10533 |
| rs146499910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11543080 | CAGTTAGATGGCGGC[A/G]TCCTCCAACCGACCC | 10533 |
| rs146512941 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11540338 | GAACATCTTTTCATG[C/T]ATTTATTTGCCACCT | 10533 |
| rs146529710 | snp | A/T | 0.0644693 | 0.167566 | intron-variant | ATG7 | GRCh38.p7 | 3:11351862 | GTTTCTTTTTTTTTT[A/T]TTATTATACTTTAAG | 10533 |
| rs146542918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11336475 | AAAGGCAAATGAATT[C/T]CCTGTTTTTCATGTA | 10533 |
| rs146543072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287740 | TATTTGCAGCATTAC[A/G]AGGTGCCTATTGCAG | 10533 |
| rs146568189 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11402811 | TAATGGAGTCAGGGT[C/T]TCATAGCCACCACAC | 10533 |
| rs146568633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333199 | AAGAAAGGAAGAGAA[A/G]AGTACAACTTGTACC | 10533 |
| rs146579214 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11399825 | GTAATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 10533 |
| rs146581891 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11525859 | GCACCTCGCCAGTTA[C/T]AGCCATTTTTAAATC | 10533 |
| rs146589465 | snp | C/G | 0.000905596 | 0.0212598 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11360667 | GCAAGGAGCTGGGGA[C/G]TTGTGTCCAAACCAC | 10533 |
| rs146594051 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11524123 | GAAATATTCTCTGTT[C/G]CATCAAAAGGAACCC | 10533 |
| rs146630392 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556394 | CCCGGCCGCCAGCAC[A/C]GCCGACCCCTCCCAG | 10533 |
| rs146674311 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11425065 | CCTCCTGAGTTCAGG[C/T]GATCCTCCCACTTTA | 10533 |
| rs146674421 | in-del | -/TAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11375039 | AGACCTCATCTCTCT[-/TAAA]AAAAAAAAAAAAAAT | 10533 |
| rs146687659 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11352125 | TCTGTCTTTGTGATA[A/C]TTTGCTCAGAATGAT | 10533 |
| rs146700460 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11420062 | CAGGTTCTTGTTCAA[A/T]TTCTTTGTGATAACA | 10533 |
| rs146700733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467440 | GCAGTGCAATGGTGC[A/G]ATCTCGGCTTACTGC | 10533 |
| rs146712328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11479257 | AAAAAGTGAATTGGG[C/T]AGGTTCAGAGCTAAT | 10533 |
| rs146713371 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11539791 | TGAGCTTTGAGAAAC[A/G]TACTCGCTTGTGGAA | 10533 |
| rs146748390 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11512719 | AAGAGTGAGCAGTAG[C/G]AAGATTTATTGCAAA | 10533 |
| rs146771180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11311510 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 10533 |
| rs146772102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319277 | TTTCCCTTCGAGCCA[C/T]GACATTTCCTTGAAG | 10533 |
| rs146779765 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11329074 | CACTCCAGCCTGGGT[A/G]ATAACGGTAATAACG | 10533 |
| rs146780174 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11374404 | ATGAATTTAGACCTT[C/T]ATTTCATACCATGTT | 10533 |
| rs146794995 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446861 | TGGGGCTGGGGAGGT[A/G]TGAGAGACATCGTGT | 10533 |
| rs146805713 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11371556 | CTTAAATCAGAAGAC[A/G]GCCTAATCCAGGGAT | 10533 |
| rs146820549 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11482647 | TTGATCAGCCTCCCC[A/G]AATTTATAGTATCCT | 10533 |
| rs146820893 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11443625 | CTCCTGGGCTCAAAT[A/G]ATCCACCTGCCTCAG | 10533 |
| rs146823363 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11542748 | CACCCCCTCCCGGGC[A/G]TCAGGTCTCTGTTTC | 10533 |
| rs146833166 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11492575 | TGTGCTCAACTCCTC[A/C/G]CGGGAGGGAGCACGT | 10533 |
| rs146846129 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11425898 | TTATATAAATGTAAT[C/T]GTACAGTACATACTG | 10533 |
| rs146858034 | in-del | -/AA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433546 | ATAAGACTAATTTAT[-/AA]GAGAGTTAATAGAAC | 10533 |
| rs146859473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527505 | GAATTTGCATTCCTG[A/G]GAACTCATGGGATAT | 10533 |
| rs146890556 | snp | C/T | 0.000354697 | 0.0133125 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333031 | GTACCATGCAGGGGG[C/T]GAGAGACGTTGCCCA | 10533 |
| rs146911783 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11356946 | AGGTCCTTTCCTGCT[C/T]TGCTTGCCACTCTTT | 10533 |
| rs146914860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432397 | TATAGATTAAAAAAT[G/T]TAAGTACCACATAAA | 10533 |
| rs146926909 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11486077 | TTTCCAATTCTGTGA[A/T]GAAGGTCCTTGGTAG | 10533 |
| rs146927377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448825 | GAATGGAGCCTCCTA[C/G]TGTTTTCTGTCCCTG | 10533 |
| rs146950188 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11483861 | TTATTCCTTGGGCTT[C/T]GTAGGCTACATTGTG | 10533 |
| rs146983451 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11529415 | TTATGTTCCCAGATA[C/T]GTGGCTTCAAACAGA | 10533 |
| rs147023072 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11452160 | AGGCTGAGGCAGGCA[C/G]ATTACCCTGAGGTCA | 10533 |
| rs147031441 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11385951 | TGGTATACGTTGTCT[A/G]ATGCTTAAAGCTGCT | 10533 |
| rs147042117 | snp | C/T | 0.00631511 | 0.0558362 | intron-variant | ATG7 | GRCh38.p7 | 3:11315513 | GATAAACTTTGAGTA[C/T]CATTTTATTATATAG | 10533 |
| rs147054028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11433874 | AAGAAAGCAACAACC[A/G]TAACATAGGCTATAA | 10533 |
| rs147065490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11533749 | CAAAATGTAGCCTTA[C/T]ATTTTGAACTTAGCA | 10533 |
| rs147090679 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11277335 | TTGCCTGCTTTTATG[A/G]CATGGTCCATCTACT | 10533 |
| rs147093680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356207 | TCATGAAAATGTTCT[A/G]TATCTTGATAGCTGT | 10533 |
| rs147113575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11273836 | CGATTCTGAAACGTA[C/T]AGGGTCATGGGATGG | 10533 |
| rs147143701 | snp | A/G | 4.23146e-05 | 0.00459951 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11332991 | AGCAGTTTCCAGTCT[A/G]TTGAAGTTGTTTGCT | 10533 |
| rs147146312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285132 | TAGGATTACAGGTGT[C/G]AGCCACCTTTTTTTT | 10533 |
| rs147157645 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11401049 | TGCTCCTGTTTAGAT[A/G]TAGCAGGCATTTTCA | 10533 |
| rs147167478 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11449435 | AGAGTCTTCACTACC[C/T]TTGGTGGCTGTACTT | 10533 |
| rs147167757 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11397936 | AAAAAATACAAAAAT[G/T]AGCTGAGCATGGTGG | 10533 |
| rs147200054 | in-del | -/A | 0.111928 | 0.208413 | intron-variant | ATG7 | GRCh38.p7 | 3:11425691 | GGATAACATATATCC[-/A]AAAAAAACACATAAG | 10533 |
| rs147225998 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11289598 | GAAGGATGTGCCTCT[C/T]ATGCAAATTACTTTT | 10533 |
| rs147233967 | in-del | -/GGGG | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555966 | CAAGTTCCAGTGGCT[-/GGGG]GTCGTTCAGCTCATG | 10533 |
| rs147248854 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11306373 | AAATGCTAGAAAATA[G/T]TATGCTGAGTTTTAT | 10533 |
| rs147254830 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531220 | CAGTCTAGAAGAAGG[G/T]GGGGCTGTGCAGGGT | 10533 |
| rs147257584 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349430 | AGTCCCAGCTACACT[-/A]AGTGGCTGAAACAAA | 10533 |
| rs147262513 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422206 | AGCCAGGCATTGACT[C/T]CTCCTCTGTAGCTAC | 10533 |
| rs147273201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11466585 | AGGCCTAGACTACAG[C/T]GTCGGTGCTTATAAG | 10533 |
| rs147273379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417127 | AATATTCCATGTGAA[C/T]GTGAGAAGAATGTGT | 10533 |
| rs147277293 | in-del | -/AAAAA/AAAAAA | 0.320096 | 0.239972 | intron-variant | ATG7 | GRCh38.p7 | 3:11538874 | TGAGACTCTTGTCTC[-/AAAAA/AAAAAA]AAAAAAAAAGAAAAA | 10533 |
| rs147284332 | in-del | -/G | 0.0520825 | 0.152737 | intron-variant | ATG7 | GRCh38.p7 | 3:11543111 | CACGGTGCAGGAGCA[-/G]CCCCACCCTGCCAAC | 10533 |
| rs147296303 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11477978 | TTCATAAGTCAGTCT[C/T]GGGAAAGGATTCTGA | 10533 |
| rs147307122 | in-del | -/CAAA | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11279718 | ACAAAAAATAAAAAG[-/CAAA]CAAACAAAAAAACCC | 10533 |
| rs147329803 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11506269 | AGTCTAGAGCTGCAC[C/T]ATCCAGTGCGGTGGC | 10533 |
| rs147333232 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11310491 | GGCCAGTGGGTGGCT[A/G]TCTACAAGGAACACA | 10533 |
| rs147366353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11369439 | CCAGCCATCCCCTCA[A/G]CAGGTAATCTGACTC | 10533 |
| rs147381401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480827 | ACTGGGTGACAGCTC[A/G]GCAAGTAGCCTCCAG | 10533 |
| rs147389290 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11364529 | GGAAATTAGTTTTTT[C/G]CTAACTTACACTGCC | 10533 |
| rs147390476 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11285941 | TGTCACGTCTTTGTG[A/G]TCTCTTTCAGTCTGG | 10533 |
| rs147390623 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11404797 | GGCTTGTGGAGGGGA[A/T]CTCCCTTTATAAAAC | 10533 |
| rs147414270 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526409 | AAAACAACAAAAAAA[A/C]CCCCAGACAACAAGA | 10533 |
| rs147437324 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11522773 | CTGTCAAATGCCCAC[C/T]CCAGGCCTAGACTGC | 10533 |
| rs147471869 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11383111 | TACTATTTTCTAATC[C/T]ACAGTCTGTGTATTC | 10533 |
| rs147486590 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11493597 | TGCCTCCCTCAATGG[G/T]TGATGCTAAACCAGG | 10533 |
| rs147487450 | in-del | -/TAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366239 | AAAAAAAAAAAAAAA[-/TAG]AACTTGTAGAGTTCA | 10533 |
| rs147494923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429544 | CATTTCCAACTTTGA[A/G]AAATCAGATCTGGGA | 10533 |
| rs147503146 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11400604 | AGTGTTGGTTCACAC[C/T]GCACCCCCCACCCCA | 10533 |
| rs147508598 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11445893 | TTTTCCTGATCACTG[A/G]TGATGTTAAACGTCT | 10533 |
| rs147508742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11505287 | TGGAGGAGTGTTCGC[A/G]CAGGTAGAGAAAAGA | 10533 |
| rs147541114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538138 | ACCTGACGGAAGGTT[A/G]GTGGCATTTCTAGAG | 10533 |
| rs147545854 | snp | A/C | 0.0197687 | 0.0974348 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270518 | AGACTACCAAACAGG[A/C]TTTGTGTGAGCAACA | 10533 |
| rs147552063 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11550744 | TGAGCCCTTTATGGT[A/C]TGTTGTTATGTTTTC | 10533 |
| rs147575233 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11546660 | GCTCCTTTCAAACTC[A/G]TCTGTCTCCTTTGGA | 10533 |
| rs147601653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277276 | GATCTATGCAGAAAT[A/G]CAGTTGCATAGCTTT | 10533 |
| rs147608739 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11341691 | GACCTCAGGTGATCC[A/G]CCCGCTTTGGCCTCC | 10533 |
| rs147622822 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11459690 | TATACTGGCACAATT[C/G]TACCTCAGGCCTGTT | 10533 |
| rs147634446 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11337530 | GTGTATGTCTTATAG[A/G]TATAGATTATATGGA | 10533 |
| rs147645558 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11456075 | GTAACCGTCATTGTC[G/T]GTTTAGAATATTTCA | 10533 |
| rs147674636 | in-del | -/AG | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557869 | AAGCACCTGAAATCT[-/AG]AGAGAGAAAGACCTA | 10533 |
| rs147677585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498892 | GAGCCAAACTGTTCA[C/T]ATCCTCATTGATCAC | 10533 |
| rs147681183 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11303319 | TCTGTTTCTGTTGAC[A/G]AGGAGGAAAATAGAT | 10533 |
| rs147713813 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11360972 | ATCAACTGTACACCT[C/G]TTCCTTGTTCACCAA | 10533 |
| rs147715161 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11282535 | CACAGTCACAAACCA[A/G]TTTGGCTGACTTGAT | 10533 |
| rs147717751 | in-del | -/ACAC | 0.21599 | 0.248322 | intron-variant | ATG7 | GRCh38.p7 | 3:11502037 | CATATATACACACAT[-/ACAC]ACACACATATGTTTA | 10533 |
| rs147726657 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11474626 | AAAAGAAAGAAAGAA[A/C]ACAGAGTGTTTGGAT | 10533 |
| rs147736062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356225 | TCTTGATAGCTGTAT[G/T]CAGTGGTTAATCTAT | 10533 |
| rs147738123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399022 | GCTGAGCAAAAGGAA[A/G]ATTAACATGTATCTT | 10533 |
| rs147749328 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11470403 | AACTGGAAAACAATA[A/G]TAAGGATTTGAGTAT | 10533 |
| rs147761036 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11518199 | TAGAGCTAGAAAGTT[A/G]ATTAGAACCATGCTG | 10533 |
| rs147778559 | in-del | -/CCCC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508044 | TAGTAGGATAAACAA[-/CCCC]CAGCCTCTACCACAG | 10533 |
| rs147781996 | snp | A/G/T | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11515157 | GTTTTAAAATGCTTC[A/G/T]TTCCTGAGAAGATCT | 10533 |
| rs147819466 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11303756 | GTTTCTTTCCCTTGA[A/G]GAATATTTGTCTTTA | 10533 |
| rs147842093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299107 | TTACTTAGCATTGCT[A/G]TGGGAAGAGATTGGA | 10533 |
| rs147852407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11413325 | TGGCTTTTATTATGT[C/T]GAGGCAGTTTCCTTC | 10533 |
| rs147856287 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ATG7 | GRCh38.p7 | 3:11485756 | GTTTCAGCTTTCTAC[A/G]TATGGCTAGCCAGTT | 10533 |
| rs147866622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535668 | CCTCTGAGGAGGGCT[C/T]GGCCCTCTCTCTTTT | 10533 |
| rs147885358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470874 | TTTATTACTTTCTTG[C/T]CGTATTACTCTCGTT | 10533 |
| rs147889760 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533316 | GAAAATGATCTCTTA[C/G]TGGTTATTTATATGG | 10533 |
| rs147906293 | in-del | -/AC | 0.0287284 | 0.116357 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557960 | CAGTAACAACAACAA[-/AC]ACACAAATGGTCAGA | 10533 |
| rs147926012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11325270 | TGGATTGGACTGAAC[A/G]AAGAGGTCAATGAAG | 10533 |
| rs147928237 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11395147 | ATAGGTGTATAGGCA[A/G]TTATATACATCTAAA | 10533 |
| rs147938044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442509 | CTTGAACTTTAAACA[A/G]TCATTAGCCATTAAA | 10533 |
| rs147938398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388976 | ATATAGGCCTGGCAT[G/T]GTGGTTCACACCTGT | 10533 |
| rs147949493 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11320001 | GTCTTCTTCCCTGTG[A/C]TCTAAGAGTAGGGGC | 10533 |
| rs147961714 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11438443 | TGGTGGCTTGTACCT[A/G]TAGTCCTAGCTACTT | 10533 |
| rs147974868 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ATG7 | GRCh38.p7 | 3:11299966 | ATCTCACTCTGTCAC[C/T]CAGGCTGGAGTGTAG | 10533 |
| rs147988255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11413645 | CACAGTTTACTGTTA[C/T]TTCATTGAGGATTTT | 10533 |
| rs147992896 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11509661 | CCACCCCTCCCCCAA[A/T]CTATCTCTAATTTTA | 10533 |
| rs147998182 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11343011 | CTCAGCTCACTGCAA[C/G]CTCCACCTCCTGAGT | 10533 |
| rs148024251 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11533805 | GAAAAGAGTAAAACA[A/G]AAGAAACTAGAAGCA | 10533 |
| rs148030354 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11292051 | CCCGTGAGTATATCA[C/T]TGCAAGAGCCGAGGT | 10533 |
| rs148065579 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11363287 | CGCTCTTGTTGCCCA[C/G]GCTGGAGTGTAATGG | 10533 |
| rs148085644 | in-del | -/AAG | 0.0876345 | 0.190099 | intron-variant | ATG7 | GRCh38.p7 | 3:11398904 | GCAAATATTTGTATC[-/AAG]AAGTCAGTAAAAGCA | 10533 |
| rs148104445 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11315659 | CCACCCCTACAGTTA[C/T]CGAATCAGCTCCTCT | 10533 |
| rs148109052 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11522262 | AGAGGTAAGTCACCA[C/T]GCAGAGGCTGGCAGA | 10533 |
| rs148114699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357806 | CTTGAGCCAAGGAGT[A/T]CGAGAGCAGCCTGGG | 10533 |
| rs148120212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | ATG7 | GRCh38.p7 | 3:11434320 | ACCCCCGTGTCAGCA[C/T]TCAGACCTGTTTCCA | 10533 |
| rs148153415 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11484396 | ACTCCGTCTCAAAAA[A/G]TGAAAAAACAAACAA | 10533 |
| rs148156899 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11310221 | ATTAGCCATATTGAT[C/G]TTTTCTCCTGCTCAT | 10533 |
| rs148161282 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492927 | ATGTTACAATGCTCT[C/G]TTAGCTCCGCCGTCC | 10533 |
| rs148170753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427038 | TTTTGTAACTTAGAG[C/T]AAATATCACTAAATA | 10533 |
| rs148180791 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11445063 | AACAATAGATGCTGG[A/C]GAGGTTGTGGTGAAA | 10533 |
| rs148192037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337980 | AAAAACTTTTATTTT[C/T]GGTTCAGGGGTATAT | 10533 |
| rs148202219 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | ATG7 | GRCh38.p7 | 3:11378347 | CTTTATCAATATGCT[A/G/T]TGTGTTTTTTAATGC | 10533 |
| rs148204271 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11480469 | TTGAGAGCATTATTG[A/G]GAGGGGGTGCGATGG | 10533 |
| rs148234585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440295 | AAAGAGCAGGTAAGA[C/G]ATAAGTCCTTTCTTT | 10533 |
| rs148258672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536636 | AGCGCACTCTGGCGG[G/T]GAGTCCCGAGAGCGG | 10533 |
| rs148274113 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11326993 | CATCACAGTTTTGTA[C/T]GGAAGCTTCAGGTCT | 10533 |
| rs148320985 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11491890 | CAGGGACATTTAAGT[C/T]TGCAGAGGTTACTGC | 10533 |
| rs148323106 | in-del | -/A | 0.0263992 | 0.111815 | intron-variant | ATG7 | GRCh38.p7 | 3:11534337 | TATATTTAGGTAGGG[-/A]CACCAGCTTGCCAAG | 10533 |
| rs148323262 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11552045 | TGCGCCACCACGCCC[A/G]GCCTCTTTCATTCTG | 10533 |
| rs148325345 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11320614 | ATTTTCTTGAGTGAT[A/C]TTTGATTAATATATT | 10533 |
| rs148336341 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288157 | AGCAATCCTTTGTGC[A/G]GTATTACGTGGCAAA | 10533 |
| rs148338560 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11404819 | TTATAAAACCATCAG[A/C]TCTCGTGAGACTTAT | 10533 |
| rs148344958 | in-del | -/A | 0.499035 | 0.0219437 | intron-variant | ATG7 | GRCh38.p7 | 3:11294018 | GCAGGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs148351833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11512779 | GAAGGGGACCTGAGC[A/G]GGTTGCCATTGCTGG | 10533 |
| rs148361341 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11453458 | AATAGCACACCCTTC[C/G]TCAGGATGTAACGAG | 10533 |
| rs148368391 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11348581 | AAGCCACGGACGTTC[A/G]CATGTTACAGCTCTT | 10533 |
| rs148373752 | in-del | -/CATACA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515705 | TCTTTCTCTCTCTCT[-/CATACA]CATACACATCAGTTT | 10533 |
| rs148374298 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11548136 | GGCATGAGCCACCAC[A/G]CTTGGACTTTTGCCA | 10533 |
| rs148378246 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11385879 | CAATTTTCTACAAAT[C/T]GTCCTCTTGTCTTTG | 10533 |
| rs148382571 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11465724 | GAGCAGTGATTGCAC[C/T]ACTGCACACCAACCT | 10533 |
| rs148412467 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11276618 | CATTGCCAGAATACC[A/T]GACCACTTTTCCTTC | 10533 |
| rs148414639 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11355249 | AGTGGAGAGACCTCA[C/T]TGAATACTCTGAGCC | 10533 |
| rs148419342 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11316933 | TGAACTTAGGATGAC[-/T]TTTTTTTTTAAAAGC | 10533 |
| rs148425353 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11469712 | GTACTGGGGCCAAGC[A/G]TGGTGGCTCCTGTCT | 10533 |
| rs148429272 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11289705 | TGGGACTACCGATGC[A/G]CCCTGCAATGCCCGG | 10533 |
| rs148434149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11394736 | AGTGGCCCGGAAACC[A/G]TAAGGCTTCCTTGCA | 10533 |
| rs148453435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11307597 | TTCTCTGAGTCTGTC[A/G]TAGCAAATCACATGT | 10533 |
| rs148457453 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11514799 | GAGAAGTATGTTCCA[C/T]GCAGGAGAAACTGCC | 10533 |
| rs148463093 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11351567 | GCCTGAGAGAGCAAG[A/T]CCAACTGTTCTTGGA | 10533 |
| rs148465448 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11423414 | CGAAGTGAGCACATG[C/G]TGTTGGAAAAATGGT | 10533 |
| rs148475546 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11467060 | ACCCGAGAGGCAGAG[G/T]TTGCAGTGAGCTGAC | 10533 |
| rs148481525 | in-del | -/CA | 0.0501905 | 0.150254 | intron-variant | ATG7 | GRCh38.p7 | 3:11535462 | GGTTTGTATGGCAAT[-/CA]CAGGGGCCAGGCAGG | 10533 |
| rs148484466 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11284795 | GCTCAAGTGATCATC[C/G]TGCTTTGGCCTCCCA | 10533 |
| rs148496940 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11402611 | CACATGCACCAGCCC[C/G/T]GTGAAAGTCAAGGCC | 10533 |
| rs148497413 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11376986 | CCTCATCATCCGCCC[G/T]CCTCGGCCTCCCAAA | 10533 |
| rs148500770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478299 | TCTTTTAGAAACATC[C/G]CATTTTGTAAGACCA | 10533 |
| rs148505277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11303073 | TATCCCTGAGGACTT[C/T]GCATTGTGTGCTGAT | 10533 |
| rs148518811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11416948 | ATCTTGAGATTTTTT[A/G]TTCATGTGTTATTGT | 10533 |
| rs148550315 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11473320 | GAAAATTGTCACTTA[C/T]TGAGTACCTGTTTTC | 10533 |
| rs148558280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373136 | AATAGGAGAACAAGA[A/G]TTGAGAGTAAGCTGT | 10533 |
| rs148603724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11530779 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGTCA | 10533 |
| rs148619019 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11318202 | GTCGGATTCAGGCAC[A/C]CTATCCTTCACTTGG | 10533 |
| rs148626266 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509610 | TTTTATTTAGTCTCA[A/G]AGGCACAGTTGTTTG | 10533 |
| rs148632186 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11437611 | GAAAATTCCCAAATA[C/T]ACCAGAAAGTTGAAT | 10533 |
| rs148641933 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11360283 | ACTCCTGACCTCAGA[C/T]AGTCTGCCCGCCTTG | 10533 |
| rs148645551 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11534766 | TTGACCACCTGGGGG[A/G]AGTCACTGTCTGCCT | 10533 |
| rs148664880 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11485417 | TGTAAATTTGTTTGA[A/G]TTCATTGTAGATTCT | 10533 |
| rs148667986 | snp | A/C | 0.040671 | 0.13668 | intron-variant | ATG7 | GRCh38.p7 | 3:11546022 | ATATGCCTGTAGTCC[A/C]AACTACTAAGGAGGC | 10533 |
| rs148685439 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ATG7 | GRCh38.p7 | 3:11429903 | GTGAGCTGAAATCGC[A/G]CGACTGAATTCCAGC | 10533 |
| rs148686046 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11493869 | GGAGAGAACCCATGC[C/G]TAGAGGACTGACTTC | 10533 |
| rs148690064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11528926 | AAGATGTTGGACTCA[C/T]GACTGCATATTCGGT | 10533 |
| rs148708501 | snp | C/G | 0.000390396 | 0.0139659 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446546 | TGATACCTACTGTGA[C/G]AAAACACACATCCAA | 10533 |
| rs148715467 | snp | C/T | 0.00236553 | 0.0343099 | intron-variant | ATG7 | GRCh38.p7 | 3:11340751 | GTATATTTGGGAAGC[C/T]GTTTTCTCCAGTCGG | 10533 |
| rs148719960 | snp | A/G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11542378 | CTAGAGCAGCCTGTC[A/G/T]CTGTGGGCTGGGAAT | 10533 |
| rs148730360 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11458651 | CTGGAACTCAGTTCC[C/T]TCTAAAAAATTGGAG | 10533 |
| rs148763346 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11501775 | GCTCACTGCAGCCTT[C/G]GCCTCCCGGGTTCAA | 10533 |
| rs148791427 | snp | C/G/T | 0.0103333 | 0.0711729 | intron-variant | ATG7 | GRCh38.p7 | 3:11399102 | CCTGTAATCCCAGCA[C/G/T]TTGGGGAGGCTGAGA | 10533 |
| rs148815680 | in-del | -/TTT/TTTTT/TTTTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471741 | GATTGGCTTTTTAGA[-/TTT/TTTTT/TTTTTT]TTTCTTTTTTTTTTT | 10533 |
| rs148824670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460243 | TGAACCTCCTTTTGC[A/G]TCTTTCATTGGTGAC | 10533 |
| rs148829053 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11543827 | GAATTGCTTGAACCG[C/T]GGACCTCTGGGGACG | 10533 |
| rs148834604 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11381700 | GCTTTACATAAACAT[G/T]TTGGACGATTTAATA | 10533 |
| rs148863652 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298853 | AGGGTTATTACTACA[A/G]TGGTAGGTGATTGTA | 10533 |
| rs148866668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336995 | ATTATTTTAAATATC[C/T]TATGTCTTCTTTTGC | 10533 |
| rs148867945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407322 | TGATTGGTTCCCATG[A/G]TCTTGGGCAGCTCTG | 10533 |
| rs148912648 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11509346 | CATGCACATTTGTCT[A/G]CATCCAGGGAGCTGT | 10533 |
| rs148916529 | in-del | -/TTGTC | 0.0944967 | 0.195752 | intron-variant | ATG7 | GRCh38.p7 | 3:11410380 | CATCAATTCAGAAAT[-/TTGTC]TTGTTGACAAATGTA | 10533 |
| rs148950852 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11396291 | ATCTTTACTAAAAAT[A/T]CAAAAATTAGCCAGA | 10533 |
| rs148952186 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11470875 | TTATTACTTTCTTGC[C/T]GTATTACTCTCGTTC | 10533 |
| rs148960897 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11291795 | GACTGTTACTGACAG[C/T]TTCATAAGGACCTTG | 10533 |
| rs148962122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504093 | GTAGATGAGACTAGA[C/G]CAACACTAAGGTTCA | 10533 |
| rs148981651 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11425970 | TCTCACTGATATATA[C/G]TATTCCATTGCATGA | 10533 |
| rs148985020 | in-del | -/CA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451900 | GACACACACACACAC[-/CA]AGACACACACACACA | 10533 |
| rs149004988 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11467893 | CTTTGAATTTTTTTG[C/T]CAAAATAATACAGAA | 10533 |
| rs149006119 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11527638 | TGAGAGTTACAATGT[A/G]TGCCCCACAATCATA | 10533 |
| rs149011642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11365362 | TTTTCAGAAAAAGAA[C/T]CCAAAGCATCATGAG | 10533 |
| rs149011664 | snp | A/T | 1.70545e-05 | 0.0029201 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362813 | ATTGTTTCTTTGCAG[A/T]CAACCAGAGACCGGA | 10533 |
| rs149012238 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287376 | AGGCAGTCACAGAAG[A/C/G]AAGGTGAGGGAGAAC | 10533 |
| rs149022488 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499764 | AAAAAAAAAAAAAAA[-/G]AAACAAAAAATCTAA | 10533 |
| rs149023085 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11304504 | TTTCTGGGTTCCCAG[A/C]GTTCCCTGTGGGCAT | 10533 |
| rs149024926 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11378213 | CAGAGGTGGGGGTTT[G/T]GCCATGTTGTCCAGG | 10533 |
| rs149034660 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11418832 | CCTCAGGAAACTTAC[A/C]ATTATGGTGGAAGGG | 10533 |
| rs149036026 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11490828 | GGCTTGTAGAGTTTC[A/T]GCTGAGACATCAGCT | 10533 |
| rs149076034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451638 | GTTGTGTCCATGAGA[A/G]AACTCCTGGGAGTTC | 10533 |
| rs149118492 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11480058 | TCAGCCTCCCAAGTA[A/G]CTGGGACTACAGGTG | 10533 |
| rs149124620 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11338396 | CATGTCTTTGATGTT[-/AA]GAGACACATTTTTAA | 10533 |
| rs149127802 | snp | A/G | 8.2603e-05 | 0.00642609 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342260 | GCACCTTGGGTTGCA[A/G]TGTAGCTAGGACGTT | 10533 |
| rs149173210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11476145 | ACCCTAAGGTGTAGA[A/G]AAAGCTGGACCTCAA | 10533 |
| rs149173491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11536444 | CCAGCTCCTTCCTAA[C/T]TGCTTTTGTTTTGTC | 10533 |
| rs149197625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11547509 | TTTTTATGTGGACAC[A/G]TTGTCATTTCTCTTG | 10533 |
| rs149198758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11282677 | TGAGTTCTCATCTTC[C/T]GGTAGAGCCTACTCT | 10533 |
| rs149202991 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11385415 | CTTAGAAAGGCAAAT[C/G]ATAGATTTGAAAGGA | 10533 |
| rs149203898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314440 | TCGTACAAATCCGAG[A/G]TTGTGGTTTTGTGGA | 10533 |
| rs149213672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432267 | GATTTAGCTAGACAA[A/G]GGAGATTTACCCTAT | 10533 |
| rs149217737 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11494901 | ACATGGTGAAACCCC[A/G]TCTGTACTAAAAATA | 10533 |
| rs149222013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328747 | CACAATGGTTATAGA[A/G]CATTTACTAGCATAG | 10533 |
| rs149227888 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532695 | GCCACTGCACTCCAG[A/T]CTAGGTGACAGAGTG | 10533 |
| rs149247750 | in-del | -/TG | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11549938 | GGAGGTGGGGTGCAC[-/TG]TCTCTTTATGGTTTT | 10533 |
| rs149261247 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11501339 | AGGGATATCAGAAAA[C/G]CTGAGAAAAGTGCCT | 10533 |
| rs149278513 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11452948 | GAAGTGCACGATTCC[A/G]TGGGCTGTAGCGAGC | 10533 |
| rs149288254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351109 | AATTCCCCCTTCCCA[C/G]TGTTTATTTGTTTAG | 10533 |
| rs149298331 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11387577 | TAGTTTGGAATTAAT[C/G]TCATTCACCTCTAGT | 10533 |
| rs149310799 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11284144 | TTTCTACAATTACTT[A/C]TTCACTTTAAAGTGA | 10533 |
| rs149311484 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11496801 | GCTGTTAATACTTGG[A/T]TCTAAAATAAACAAA | 10533 |
| rs149318575 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273777 | TAATAATAGTGGTGG[G/T]GGTGGCGGTGGCGGC | 10533 |
| rs149322323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11400367 | AATAGGGGTAGGCCA[A/G]TAAATCAATGAGCAG | 10533 |
| rs149343552 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11345653 | TTTTCCTCATATTAA[A/G]CCTTGCTAGAGAGGC | 10533 |
| rs149346330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545506 | CGCTCCTTCCTCTCT[A/G]CTCTTTCCTGCCCCT | 10533 |
| rs149354734 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11462296 | AGATAGTCTGTTAGG[A/T]GCAGCCACAAGAAGG | 10533 |
| rs149355759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520666 | CACTTCTGAGCTCGC[C/T]CTGTACCTCACAGCA | 10533 |
| rs149361497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11357624 | TTAAATCAAATTATA[G/T]TTGCTAGAACACTCC | 10533 |
| rs149362872 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11278400 | ATGTCCATATTAAAA[C/T]GAAATCTTCGCAATT | 10533 |
| rs149366792 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557904 | CCTGTATGAGACTTC[C/T]CCTTCCAAAGCTGTA | 10533 |
| rs149395919 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11410268 | CATATGTACATCTTG[A/C/T]ACACATTTTGTTAGA | 10533 |
| rs149399908 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389816 | TCTTGGCAGCTAAGG[G/T]GTCTTTGTAATTGAC | 10533 |
| rs149410126 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | ATG7 | GRCh38.p7 | 3:11516297 | CATATGTAACAAACC[C/T]GCACGTTGTGCACAT | 10533 |
| rs149427034 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11302508 | ATGTGCAGATGTGTG[C/T]GTGTTAGGAATACAA | 10533 |
| rs149434069 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480587 | AAACAGACAAAAAAA[-/A]CCTTACAATCTGTGC | 10533 |
| rs149438838 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11416350 | TGGTGCTTTCTATTT[A/G]GGAAGGTTATTAATT | 10533 |
| rs149439317 | in-del | -/AAAAT | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11345410 | CAGGACTCTGTCTCA[-/AAAAT]AAAATAAAAGAATTT | 10533 |
| rs149464182 | in-del | -/CTGAGGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306112 | CTGACTTTGCTTACT[-/CTGAGGA]CTGTGAGGCCTTTGG | 10533 |
| rs149471206 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11472850 | CGCTGATTTGCACAC[C/T]GTTTTTCATGAAATC | 10533 |
| rs149493018 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ATG7 | GRCh38.p7 | 3:11484263 | GCCAGGTATGGTGGC[A/G]TGCACCTGTAATCCC | 10533 |
| rs149515026 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11429821 | GGTGTGGCAATGTGC[A/G]CCTGTAGTCCCAGCT | 10533 |
| rs149520814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11326423 | CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGACTA | 10533 |
| rs149524698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469050 | ATTTACACAATTAAG[C/G]TAGGCCCATTGTGAA | 10533 |
| rs149537713 | snp | C/T | 3.31329e-05 | 0.00407005 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426844 | GATTTAACTTCCTAG[C/T]CAAGGTGTTTAATTC | 10533 |
| rs149553737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380408 | TTAAAGCGTTACTCT[C/G]AGGGTGAGGCGGCCC | 10533 |
| rs149555155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11306328 | GAGCTTAGTGTCCTC[C/T]AGCTGGGTGGGTATG | 10533 |
| rs149564966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422069 | ACAGGCAGAGAAGAT[G/T]TAGCATAATTTTTAA | 10533 |
| rs149568621 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ATG7 | GRCh38.p7 | 3:11491854 | TCTCAGAGGAGTACC[C/T]GGCCGTGTGAGGTAT | 10533 |
| rs149576265 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11525806 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10533 |
| rs149605159 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11376265 | ATAGTGATGATGGTT[A/G]CAAAACTGTTCATAT | 10533 |
| rs149653138 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11542216 | TGCTTCTAACCAGTG[C/T]TTGGACAAGCCCTTG | 10533 |
| rs149658665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11275732 | ATCAAGGGACAATAA[A/G]TACTGGAGGTGCTGC | 10533 |
| rs149660400 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11492486 | GCCATCTTGGCTCCA[A/G]CCCCTCCAGGATATT | 10533 |
| rs149664163 | in-del | -/AAAGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517359 | AAAAAAAAGAAAAGA[-/AAAGA]AAAGAAAAAAACAAT | 10533 |
| rs149668754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11324049 | TGATCATGACTGAAT[A/C]ATTTCAATGAATTGT | 10533 |
| rs149672790 | snp | A/G/T | 0.0213559 | 0.101272 | intron-variant | ATG7 | GRCh38.p7 | 3:11424572 | GGTGTATTTATTATC[A/G/T]GTGGCAATTAAATAA | 10533 |
| rs149706433 | in-del | -/AT | 0.0711525 | 0.174681 | intron-variant | ATG7 | GRCh38.p7 | 3:11344126 | TGGGATGTAGGAAAA[-/AT]AGTGAATTTTGCATA | 10533 |
| rs149707150 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271010 | TACTATCTGATCAAG[C/G]CACCCCTTCATCCCA | 10533 |
| rs149714382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549336 | AGGAAATTAACACAT[A/C]TGTGAACTCCCATAG | 10533 |
| rs149715399 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487119 | aaccctgagtgggca[C/T]agcacatgtttcaga | 10533 |
| rs149735766 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298798 | TTGACCCAGAAGAAG[C/G]TGAACGAGTATCGGC | 10533 |
| rs149752334 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11381444 | GAAATAAAGATAATT[A/G]GGTTCTCTAAGTGAA | 10533 |
| rs149799059 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11539731 | TTTAAAAAATAAAAT[C/G]TATTGATGCGCATAC | 10533 |
| rs149808009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11377607 | AGTTTGATGAAAACC[A/G]TATTAGAGAAAACAG | 10533 |
| rs149809800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455439 | TTGCTGGTCCACATT[C/T]GGTGGTCCACTCATA | 10533 |
| rs149819403 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | ATG7 | GRCh38.p7 | 3:11467501 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGATTAT | 10533 |
| rs149826899 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11286405 | TGGCATATCGTCGTA[C/T]GTTCTTCATGATTCC | 10533 |
| rs149828489 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11388832 | CATGGACTTGTAACT[A/G]CTACCCAGCTGCTGA | 10533 |
| rs149843364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498465 | TTTCCTTCACTTGCT[A/G]TATGGGCCACCTGCC | 10533 |
| rs149850220 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11332480 | AAAAATATGAAGATA[C/G]ATAAATTATAGATTG | 10533 |
| rs149850660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11402427 | AATAGAGTGAGACTC[C/T]GTCTCAAAAAATAAA | 10533 |
| rs149874546 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11523367 | CCTTGGTGACCCACC[A/G]CATACGGGGTACATC | 10533 |
| rs149878622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360032 | TAAGAAATGTTTGTT[A/G]TGAGTTTTTTTGTTT | 10533 |
| rs149889133 | in-del | -/CCCCCCC | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11288664 | TTTCTTGGGAGGCAA[-/CCCCCCC]CCGCCACTGCACATT | 10533 |
| rs149889258 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280793 | TTAGCCCCAGCACAG[C/G]GTTCAGTGCACATGA | 10533 |
| rs149904574 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11397797 | TAGAAAATTTTAATG[A/C]ATCGGCTGGGCGCGG | 10533 |
| rs149923756 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11311356 | TGCCTGTAATTCTAG[C/T]GATTTGGGAGGCCGA | 10533 |
| rs149925101 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11517831 | TGGGGCCGTGCCATG[C/G]AAGGCTTTGCCAGCT | 10533 |
| rs149943158 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11340687 | AGAACCAGAAAGGAG[C/G]CATGGGACCAAGGAT | 10533 |
| rs150008487 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298587 | TAAACATCTCATTAC[G/T]TTTTGTTTGTTTGAA | 10533 |
| rs150018760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11412040 | CTGCTTGGTGCACAG[A/G]AAGCCAATCACTGAG | 10533 |
| rs150020330 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11485337 | GGCTGCATAAATGTC[A/G]TCTTTTGAGAAGTGT | 10533 |
| rs150038692 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ATG7 | GRCh38.p7 | 3:11328148 | TCACCACTGGAGATT[C/G]TGAGTCTATCACCAA | 10533 |
| rs150041185 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11431396 | GGCGGGGGGAAAAAA[A/G]CAACCACACACAACA | 10533 |
| rs150049672 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11446166 | TGGGTTAGAGCAGCA[A/G]TTCTGAACCTTGGCT | 10533 |
| rs150054447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532355 | AACAGAGGAGGAAAC[A/G]GAGGAGGACAGAGCT | 10533 |
| rs150061502 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11371270 | TAAGTGCTTTAGCAG[A/G]GGGACGTAGAACAGG | 10533 |
| rs150072901 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11481801 | TTTGAGTAGGGGTGT[A/G]GCTGTGCACCAGTCA | 10533 |
| rs150101240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375945 | GACCCAGTAATTCTA[C/T]TCCTAGGTATATTTC | 10533 |
| rs150112420 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11300053 | CCTTAGCCTCCCAAG[C/T]AGCTGGGACTACAAG | 10533 |
| rs150115586 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11486726 | CATCAGTACCTAATT[C/T]ATTGAGAGTTTTTAG | 10533 |
| rs150123181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313125 | GACTATTTTGGGAAT[A/G]CAAAAGTCCTTTATT | 10533 |
| rs150137241 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11495265 | AGAATTAAGGATCAT[A/G]GGATGAATGATGAAT | 10533 |
| rs150146695 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11329726 | TCCCATGTACCTTCA[C/G]CCAGTTTCAGTTTTT | 10533 |
| rs150147341 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11534083 | GCCTCCTCCTCCCCC[A/C/G]CCAGGGGAAAGCTGC | 10533 |
| rs150155856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448553 | AACCAAATCTGTAAT[C/T]AGGAACATAAACCAA | 10533 |
| rs150179126 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11483309 | AGCTTCATCCTATTT[G/T]CCAGCTGCCCAAAAT | 10533 |
| rs150190714 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11493104 | AAAAGAATGAGGTCA[C/T]GTAGACGAATTGAAG | 10533 |
| rs150193137 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557016 | AACCGGGGGTCATAC[A/G]GTGTGCAGAGTCCAC | 10533 |
| rs150196298 | in-del | -/CTG | 0.0744748 | 0.178019 | intron-variant | ATG7 | GRCh38.p7 | 3:11448369 | TCTCTCTGGCTGCTT[-/CTG]CTCACCCAGGGTGGA | 10533 |
| rs150198390 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11325625 | ATGGTGAGCTGAGAT[C/T]GTGCCATTGCATTCC | 10533 |
| rs150198875 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11395887 | GGAGCTCGCAGTGAG[C/T]GGAGGTCACACCACT | 10533 |
| rs150236884 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11272932 | TCCTTGGTTACAGGG[G/T]TAGAAACTAATGCAC | 10533 |
| rs150244237 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11551585 | TTTTCACTGCTTTTA[C/T]AATTTTTTTTAAAGT | 10533 |
| rs150258952 | snp | C/G | 3.30978e-05 | 0.0040679 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313400 | CCAGTGGGTTTGGAT[C/G]AAAGGTTTTCACTAA | 10533 |
| rs150272600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461499 | AGGCATTCAAAACCT[C/T]GTTTTGCAGGTTAAG | 10533 |
| rs150279792 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11277900 | TTATAGACCCCCCCC[C/G]CCCCACCAGGAATGC | 10533 |
| rs150283645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11382604 | CCTTATTTGACGTTT[A/G]TATGAGTTGCTCTTT | 10533 |
| rs150308973 | in-del | -/TA | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11472425 | CAGTGACCCTGTCAC[-/TA]TGGTAGAGGAAGGGG | 10533 |
| rs150312387 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11408620 | AGGCCTTACAATCCT[G/T]GTGGAAGGTAAGGAG | 10533 |
| rs150326108 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ATG7 | GRCh38.p7 | 3:11515374 | AGTGGCACGATCTTG[A/G]CTCACTGCAACCTCC | 10533 |
| rs150327032 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11541341 | AGATTGTCCTTTCTC[A/G]TCAAATTACTGTGCC | 10533 |
| rs150335988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457600 | GGATCAGGGGGAAAC[A/T]TTTCCGGAACATACA | 10533 |
| rs150350967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288565 | TGTATTGTTTTATAT[A/G]CATAATACAAACTTT | 10533 |
| rs150353546 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11367543 | GTGCTCTCTGGGTCT[C/T]TGCTCTCCTCTGTGT | 10533 |
| rs150366654 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11479768 | TATGCATTGTCCCTC[A/G]GTTGGTTTTTAATAA | 10533 |
| rs150368539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11500174 | GCGCAACATAAAGAA[C/T]AATATGAACACAGTT | 10533 |
| rs150398990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465972 | AAAGTTGGTACATTC[C/T]TTTCATTTGTGTCTT | 10533 |
| rs150408758 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11361333 | CCTGTCACCCAGGCT[C/T]GAGTGCAGTGGCACA | 10533 |
| rs150420216 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11475780 | GATCTTGCAAAACCT[G/T]TTGACCCATTGATAC | 10533 |
| rs150454282 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | ATG7 | GRCh38.p7 | 3:11519660 | CCCCTCCCAGATTCA[C/T]GCCATTCTCCTGCCT | 10533 |
| rs150492936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320058 | GTCTGTGTGGCCTGG[C/T]CCCTGTGGGCATCCA | 10533 |
| rs150495667 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11421201 | GTTGGGGTGGCTGTG[G/T]CATTTTCTTAGAAAA | 10533 |
| rs150527953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11477666 | GTTGCAAATTTTAAC[A/C]AACCTGAACAAGGGG | 10533 |
| rs150558845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11435905 | GAACAGCATTTTGCA[A/T]ATCATACCTGATAAG | 10533 |
| rs150601005 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11323492 | GTGGATTCCACAGTC[A/G]CACTCCATTGCTACA | 10533 |
| rs150623569 | in-del | -/TATTGT | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11475133 | GGGCAAGGTAGATTA[-/TATTGT]TATTGTTATTGACAT | 10533 |
| rs150629792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11352361 | TAATTCTTTGGGTAT[A/G]TACCCAGTAATGGGA | 10533 |
| rs150643138 | snp | A/G | 0.499784 | 0.0103811 | intron-variant | ATG7 | GRCh38.p7 | 3:11490153 | TTGCTTTATGAATCT[A/G]GGTGCTCCTGTATTG | 10533 |
| rs150643940 | in-del | -/TTTGGGCTATCATGAATAGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426044 | TCAATGGTTTCTAGT[-/TTTGGGCTATCATGAATAGC]GCTGCTGTGGACACT | 10533 |
| rs150651298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387258 | CTGCAGAAACCTTCC[A/G]TTCATGTCTCTTGAC | 10533 |
| rs150662518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332182 | GTATATCCCTTATGA[G/T]GAAATGTCATATACA | 10533 |
| rs150677869 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11535431 | CAAAGTCTTCTGCGT[C/T]GGCCCTCCCTGAGCA | 10533 |
| rs150683066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11344921 | ACTTCATAAGTCAAA[C/T]TGGTTTATAGTCATG | 10533 |
| rs150684939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373414 | TACAGAGCAAACCAC[A/G]GGAGGGTGTAACTAA | 10533 |
| rs150696348 | in-del | -/AC | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11431408 | ACAACACACACACAC[-/AC]CTTTTTAAAGTGTGC | 10533 |
| rs150697108 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11545379 | GGTGACGGATACCTG[C/T]GGGGACAACAGATCC | 10533 |
| rs150717420 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11494243 | CTACATGCAGGAAAA[C/T]AGGAATTAGGGAGGG | 10533 |
| rs150723126 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11327338 | TTGTGTATATTTATG[C/T]AGTGAACCCTCTTTT | 10533 |
| rs150723940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11294735 | CAAACTCCAGACTCC[C/T]GGCCTCCATCACTAT | 10533 |
| rs150726958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505073 | TAACTAAAAGTATCA[A/G]GTAAGTCTCTACGGA | 10533 |
| rs150727567 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant, synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11380049 | TACAGCTTGTTCTTC[C/T]AAAGTAAGTCATTTT | 10533 |
| rs150738250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445315 | CTTAAATGCCCATCA[A/G]TGGTAGACTGGATAA | 10533 |
| rs150759904 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ATG7 | GRCh38.p7 | 3:11553132 | TCCATCTTGCCCCAT[C/T]ACCTCCCACCTCGGC | 10533 |
| rs150765822 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11392362 | ATTTACTTGAAGTAG[G/T]GTAGCTTTCTCCCAT | 10533 |
| rs150767047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11468834 | CAACAGATACCATCT[C/T]TGGTCTAAAATAGAT | 10533 |
| rs150799786 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11464378 | ACCCTGTCTCAAAAT[G/T]AAAAATTAAAAAATT | 10533 |
| rs150806260 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11280256 | TTTCGCCATGTTGGC[C/T]GGGCATGTTATTGGT | 10533 |
| rs150839259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11340788 | TGTAACCAAGACACA[C/T]ACCAAGTTCTGTCAG | 10533 |
| rs150843968 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11411082 | GAAGTCTTTTTTTAT[C/T]GTCACATGCTCATCA | 10533 |
| rs150853781 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11458920 | GATTCTCATAGGGGC[A/G]GGAACACAATTGTGA | 10533 |
| rs150854976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11517210 | GTTGGGGATGGTAGC[A/G]CATGCCTGTAATCCC | 10533 |
| rs150858630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274830 | AATACTCAATAAACA[A/G]TAGTCATTAATATTG | 10533 |
| rs150874382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11369956 | ATTTTACAAAACCAG[C/T]TGGGGCAGCTCTTAG | 10533 |
| rs150881583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11290192 | ACAAGTAGGTCATAA[A/G]CAAATTATGTCTGCA | 10533 |
| rs150885586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481387 | AAAGTCAAGGTGAAC[C/T]ATGTATTTGCTGTAA | 10533 |
| rs150893622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305594 | TCCCTTTGTGATTTC[C/T]CTCTCTTCAAGACCA | 10533 |
| rs150909381 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11513320 | CGTTGGGGAGGCTCG[A/G]GCTGCACAGGAGCCC | 10533 |
| rs150939393 | in-del | -/T | 0.0577344 | 0.159793 | intron-variant | ATG7 | GRCh38.p7 | 3:11492546 | GACAGGGGTTCCCTG[-/T]TTACTCAGTCCGTTG | 10533 |
| rs150949511 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11312191 | AAATTATATCTCAAT[A/G]AAAAGTCATCTAACA | 10533 |
| rs150952104 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11518487 | AGAAGGTAGAGGTTG[C/T]AGTGGCCTGAGATCG | 10533 |
| rs150959595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356038 | GCAGTATGCTAAGCA[A/G]AAGAAGCCAAACACA | 10533 |
| rs150961014 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11460773 | TAATGATTATTCTTA[A/T]AAAGTACTGAGGGAA | 10533 |
| rs150982961 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372035 | TTTTGCATGCTGTCT[G/T]CCGTGTTTTCATTCC | 10533 |
| rs150991065 | in-del | -/TCAGTCTTTC | 0.0352966 | 0.128072 | intron-variant | ATG7 | GRCh38.p7 | 3:11470889 | CCGTATTACTCTCGT[-/TCAGTCTTTC]TCCTTTGAGGTGCAG | 10533 |
| rs150991311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407644 | TCTGAAATCTAGGCA[G/T]AGGTTCCCAAACCTC | 10533 |
| rs150992729 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11483031 | CTCAACGTTTTTCCA[C/G]CTATACCCACCTCTA | 10533 |
| rs150994807 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11362276 | AGAGCCATGTTGTAG[-/A]AAAAAAAAATACTTG | 10533 |
| rs150998413 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11308102 | CCCCCTCGGCTTACC[A/G]GAAACTGGGGGCCTC | 10533 |
| rs151013239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11423842 | TGACCTTAACCTTTT[A/G]ATCCTTATTCTGCCA | 10533 |
| rs151027519 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11528090 | TGCCTTCTCATGTTG[A/G]GGACCAACATGAGAA | 10533 |
| rs151028950 | in-del | -/GTGT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372854 | GCGTGCGTGTGCGTG[-/GTGT]TGTGTGTGTGAAATC | 10533 |
| rs151031489 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11365496 | TGAAGAGGTTTTCCA[A/G]TCTTATTTGGAAATC | 10533 |
| rs151046389 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11478917 | TTAAGCTCTGGGTAA[C/T]TTAAGTGGCTGTAGA | 10533 |
| rs151077537 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11497806 | CATTCACTGCTATTA[C/T]AATAATAATAGTTTA | 10533 |
| rs151107232 | in-del | -/G/GG/GT/T | 0.481655 | 0.117796 | intron-variant | ATG7 | GRCh38.p7 | 3:11326285 | GAGTTGTAAATGCTG[-/G/GG/GT/T]GTTTTTTTTTTGTTG | 10533 |
| rs151136027 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11549075 | GCAGCTTTTTTTTTT[-/T]CAATCAGCTGTATTG | 10533 |
| rs151156601 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272553 | TCTCAGGATCCTCCT[C/G]TGCCAGTTTCTGGGT | 10533 |
| rs151163734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551335 | AACCAGCTCGCCCGG[C/T]TCCAGAAAACATTTG | 10533 |
| rs151179759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319046 | TTTGTCCCCACTCTG[C/T]GTCCTCAACATTTAG | 10533 |
| rs151181368 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11437490 | CGTTGCTATCTGTTT[-/G]TGTAAGTTTAAGCAG | 10533 |
| rs151190085 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11333742 | TGCCCAGCTCCGGAT[A/G]TATTTCTTTTTTTTT | 10533 |
| rs151195420 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11403250 | AGGAAGTCTTGACAA[G/T]AGTCTTTTGGAGTGC | 10533 |
| rs151205133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11451985 | ACAATCCATAGAAAC[A/G]TAAAAACAGATTCAT | 10533 |
| rs151206995 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ATG7 | GRCh38.p7 | 3:11511792 | ACAGCACCGGTGGGC[C/T]GGTACTGCTGGGGTA | 10533 |
| rs151214552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11347061 | GCTTACTTATGATCT[A/G]CTAAAATATACCCAC | 10533 |
| rs151215552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11546233 | CTGGAGTGCAGTGGC[A/G]TAATCTCGGTTCACT | 10533 |
| rs151224307 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11383931 | TCTTAAAACAACTCC[A/G]TAAGTTTTAACAAAT | 10533 |
| rs151236290 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11475430 | TGGGCAGGGGGCTGG[C/T]GAGATGCGTCAGGAT | 10533 |
| rs151238255 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ATG7 | GRCh38.p7 | 3:11495037 | AGATTGCACCACTGC[A/G]CTCCAGCCTGGGTGA | 10533 |
| rs151245457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11399223 | TATGGTGGCCTGTAC[A/G]TATAGTCCCAGCTAC | 10533 |
| rs151252512 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297820 | TTCTGAGTGGCTGGA[G/T]TTAGGATTTTGTACT | 10533 |
| rs151256873 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11507522 | ATCCATAAGTATAAT[A/G]TGATATGAAAATACC | 10533 |
| rs151278045 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11301683 | TTGGCAAACTAACTT[-/A]ATTTTGGAGCCAGTA | 10533 |
| rs151291079 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555729 | CTCTTTATTCTGGGT[A/G]TGTGCAGCTGTGAGG | 10533 |
| rs151299146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11470040 | TGTACTGGGCTGTGC[A/G]TGCTTCAGCTACCCA | 10533 |
| rs151328565 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11361077 | TCCGTATTGTCTCCG[A/G]TGCTTCTCTTAGTCA | 10533 |
| rs151332368 | in-del | -/TGG | 0.0174175 | 0.0916809 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272192 | AGACATTCCGACATC[-/TGG]TAAGGGAGACGCTCT | 10533 |
| rs151336485 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11282918 | TATGCTGTTTGTCAG[C/T]GGGACTTGGTCATGT | 10533 |
| rs180673187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509848 | TGTTTAAATATCTTC[A/C]CATAAATCAGGCAGC | 10533 |
| rs180689902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491649 | GTACAGTTGGGTTTT[C/T]GGTGTGGATGTCCTT | 10533 |
| rs180696588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11473306 | CACCTACCCAGGAAG[A/G]AAATTGTCACTTACT | 10533 |
| rs180702761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501653 | TCTCAGGGAATATAT[A/G]CTGATATATTCTGAG | 10533 |
| rs180716947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456463 | GTGTACAAGTTGTTG[A/T]ATGAAGTACACGTTT | 10533 |
| rs180717700 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11436600 | TGTGCACACAAAAAA[G/T]GTACACAGTGTTCCT | 10533 |
| rs180719472 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11463138 | GATCTGCCCTCCTCC[A/G]CCTCCCAAAGTGCTG | 10533 |
| rs180725561 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11480710 | CTTTGCTCACAAGGA[A/C]TTGAAACCCAGGCTT | 10533 |
| rs180750664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314939 | AAAAGTAGTAAATGG[A/G]TGAGTTGTATGGTAT | 10533 |
| rs180760137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368766 | AAGGAATCAAGGTGA[C/T]GCTACAACAGTTGTC | 10533 |
| rs180764177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523462 | TGTATGACTTGTTCC[C/T]GGACAACCCATTCTT | 10533 |
| rs180766678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388218 | AAGGGAGATGCAGGG[C/G]CTGATTTACCACTAG | 10533 |
| rs180789149 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11340797 | GACACACACCAAGTT[A/C]TGTCAGGCCAACACA | 10533 |
| rs180799288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11379742 | GGTCAGAAATATTTG[A/G]AAAGCTTGTAAGCCC | 10533 |
| rs180806500 | snp | A/G | 0.00195198 | 0.0311798 | intron-variant, synonymous-codon | ATG7 | GRCh38.p7 | 3:11446513 | TTTACTTTTAGCACT[A/G]AGAAGATTTTCTTAC | 10533 |
| rs180813719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11426032 | TTGATGGTCACCTCA[A/G]TGGTTTCTAGTTTTG | 10533 |
| rs180816646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11418197 | GCAGCCTCAACCTCC[C/T]GGGTTTAAGCCATCC | 10533 |
| rs180819315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407729 | CTTGGGGCTTGCATT[C/G]TCTGAAGCCATGGCA | 10533 |
| rs180820532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11273432 | TCACTGTTCCTCCTT[C/T]AGGCTCTTGGAATCA | 10533 |
| rs180821057 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11358873 | TACTTACATTAAAAC[A/G]TAAGCTCCAAGAGGA | 10533 |
| rs180828434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295611 | CCTTTTAAACATTAA[A/G]TACAATGTTTAAATG | 10533 |
| rs180829623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328072 | TCAAGTCCATGGAGT[A/G]GACCAGCTGCATCAG | 10533 |
| rs180833166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11348139 | GTCAGATATCTGTCA[C/T]TTTCTACCAGCCACT | 10533 |
| rs180845050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305637 | TCATCTCACCTGGAT[A/G]AAAAATATTCTTTTA | 10533 |
| rs180860472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282202 | ATGTAGGCTTCTCAA[A/G]CCCCATAATGCTGGT | 10533 |
| rs180865961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11403715 | AAAAGGCAAGGAATA[C/T]AAAAACCAACAACAT | 10533 |
| rs180888859 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11393538 | GGAAATATTATGTCT[A/T]GTATAATGTTGCCAG | 10533 |
| rs180904493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320775 | GAGTTGTGAAGACTG[A/G]AGATTGCTCATGGGA | 10533 |
| rs180929177 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469269 | AGCCTGACCAACATG[G/T]AGAAACCCCATCTCT | 10533 |
| rs180930788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11451931 | CACATATACATATCT[C/T]TTAAATGAGATTCTA | 10533 |
| rs180933731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476376 | ATGCGTCAACAATGG[C/T]TGGTAGCTGCCACCA | 10533 |
| rs180935784 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11495389 | ATCCTGAGGAGAGAT[A/G]AGGCACTGAAATCCA | 10533 |
| rs180937495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431792 | TCTGTCTCCCTAAAT[A/G]TAGCCCCTTTATGAA | 10533 |
| rs180938171 | snp | G/T | 1.71666e-05 | 0.00292968 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362908 | GGAATTGATGGTATC[G/T]GTTTTGCAGCATCCA | 10533 |
| rs180948973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355112 | TGACTGAATAGCGAG[C/T]TGTGTGTACTCACAG | 10533 |
| rs180952693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336395 | AAAAGGTTTTCTGTC[A/G]TCCACTAATGCCTTT | 10533 |
| rs180957907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373045 | ATGTGTTTATCGTTT[C/T]TATTACAGAAAGAGT | 10533 |
| rs180969962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343798 | CTTATATACCTGAGT[C/T]TCTTTATGGATTCTC | 10533 |
| rs180971804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11300969 | AATTTATGATGAGTT[C/T]ATCAGGACATGGTAA | 10533 |
| rs180974272 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11278157 | ACACACATGTTTTAC[A/G]ATCAATTTGTACAGT | 10533 |
| rs180977185 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310733 | TGCCTCCCAGGTTCA[A/C/T]GCCATTCTCCTGCCT | 10533 |
| rs180986964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11382852 | AGTACAAGGAACTCC[A/G]GTATACACTTTACCC | 10533 |
| rs180988979 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11458614 | AACACATTGTGTGAC[C/T]ATAGCTAGTTACTTC | 10533 |
| rs180996830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422842 | TCACTGCAACGTCCG[C/T]CTCCTGGGTTTAAGT | 10533 |
| rs181052385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321948 | CAACTCTGCCTTTAC[C/G]AAAGGAAGGCATAAG | 10533 |
| rs181053845 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11301415 | AGTGGCAATGGTCAA[C/T]TATTAGGATATTTAA | 10533 |
| rs181062997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344231 | CCTCACCAACACTTA[C/T]ATCTTCCTTTTCCTT | 10533 |
| rs181097119 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287438 | GTTCTAGGCCATGGG[C/G]GCCTGAGAGCGGCTG | 10533 |
| rs181102768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278676 | TTGTTTCAGTCATCA[A/G]CAAGTATTTATTGGG | 10533 |
| rs181110810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11335129 | GCTTGATCAAAGGAC[A/G]ATGCTGCTTTTCAGT | 10533 |
| rs181111154 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309955 | GAGGCAGGTGGATCA[C/G]TTGAGGCCAAGAGTT | 10533 |
| rs181121012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11353893 | TGAAATGGACTAACA[C/T]AGGAAATACAAAGAA | 10533 |
| rs181124485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372259 | TGGGTTTTTTAATAT[G/T]CAGGGAGTAGCAAAG | 10533 |
| rs181130216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11531606 | GGCCAGGTGCAATGG[C/T]TCATGCCTATAATCC | 10533 |
| rs181136291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391431 | CAATGTTAAGCCTAC[A/G]ACTTTAGATGAGCTG | 10533 |
| rs181150164 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516014 | CATACGTTTTGGGAA[C/T]AGCTCACATTCCTTT | 10533 |
| rs181214756 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510591 | CCCACATCCAGCACA[C/G]TAAAAGCAGGCTGTC | 10533 |
| rs181219987 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11523991 | ATGTTGACACTAGCT[C/G]TGGGAACTCTGTGAT | 10533 |
| rs181239369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549247 | CTGTGTTAGGGTTGT[G/T]TTCTTAAAAACTGTA | 10533 |
| rs181280056 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11442833 | GGCTGAGATGGGAAG[A/C]TTGCTAGAGCCCAGG | 10533 |
| rs181295759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423142 | TTGTAATTGGCCTAC[A/G]TTCAGTATTGTTTTG | 10533 |
| rs181300474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404629 | GTTGTATTAGTCTTT[C/T]TCATGCTGCTCATAA | 10533 |
| rs181300591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450563 | TACCATTCTCCATAA[A/G]TACATGGGAGACAAC | 10533 |
| rs181306768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430576 | ATTATATGTGACATT[A/G]CCATTATATACTTTG | 10533 |
| rs181313625 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11553567 | GGGGGAGTTTCCAGC[C/T]GCACTGAGGATGAGC | 10533 |
| rs181320639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364495 | ATGTTTAAATTACTC[A/T]TCTTGCCCTTTGTCC | 10533 |
| rs181325445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383357 | GTTTCCCTATGATTC[G/T]ATTCAGGTTATGAAT | 10533 |
| rs181363391 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11458829 | TGTTAGGAACCCGAT[C/T]GCGCAGCTGTAGGTG | 10533 |
| rs181371861 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11497067 | TGTTGGCCAGGCTGG[A/T]CTCAAACTCATCAAC | 10533 |
| rs181371950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11537626 | ACTACACATGCAACA[C/T]GAACTCCTCAGTCAA | 10533 |
| rs181378027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478057 | CGAGTAAATAGCACA[A/G]TATGATTATCCTGCC | 10533 |
| rs181379627 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11459061 | TTCCTCAAGACTGGT[C/G]CCTGGTGTCAGAAAA | 10533 |
| rs181383979 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11443391 | GGTTTCCTTTTCTTC[A/G]TTGTTGTTTTTTGAG | 10533 |
| rs181432905 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11528059 | GTCCCTTCTGCTTCA[A/G/T]TTGTGGGCCTTCTGT | 10533 |
| rs181436005 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11552627 | AGCCCGTCCCTGCCC[C/T]AGAGATTCGCTCTGG | 10533 |
| rs181438310 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11527794 | TAAAAACTCAAGTTA[C/G]AGTTATATAAGGCCT | 10533 |
| rs181442017 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11512690 | TTACAGCTCATAAAA[C/G]CAGTGTGGACCCAAA | 10533 |
| rs181443836 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11496295 | GGGTCACTTCCTAAT[A/C]CCTGAATGGGTTCGC | 10533 |
| rs181469374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519292 | CTTGGGTACTATCAT[A/C]ATCCCCATTTTAATG | 10533 |
| rs181499958 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487015 | TCCCTGATTACTTGA[C/G]ATGAGGGATTGGTGA | 10533 |
| rs181511403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451667 | TCTACACTCAGCAAA[C/T]GTTTGTTGTTGGACT | 10533 |
| rs181523140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11335844 | CTGGGATTACAGTCG[C/T]GTGCCACCACGCCTT | 10533 |
| rs181529702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354371 | GTCAGATTATGAGGC[C/T]GGGCGCAATTGCTCA | 10533 |
| rs181535497 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372817 | GTGTGTGTGTGTGTG[C/T]GCGCGTGTGCGTGTG | 10533 |
| rs181538236 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11546785 | CCCCTAATGCAGAGT[A/G]GCAGCCCATCCCTGC | 10533 |
| rs181542655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411723 | CTGTTGATGTTGTCC[A/C]TCTATGAAATTCAGT | 10533 |
| rs181560951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546370 | AGAGAGGGGGTTTTG[C/T]CATGTTGGCCAAGCT | 10533 |
| rs181582769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287620 | GCAGTCTTTCCGGAA[C/T]GTTATGAGCCTTAAT | 10533 |
| rs181584904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482575 | GTACAGTTGGGCCTT[A/C]CTGAGAGCTAGAATT | 10533 |
| rs181586014 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11501838 | GGGATTACAGGTGTG[C/T]GCCACCACATCCGGC | 10533 |
| rs181590233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11512103 | TGGGAGCCCAGGCAG[A/G]GGAGGTGCCAAGAGC | 10533 |
| rs181591154 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11310351 | ACATTAATCCTCTTT[A/C]CCACTTCTTTTTTTG | 10533 |
| rs181593891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477713 | GTAGTTGGAATGTTA[C/T]TGGAACTACTCATAG | 10533 |
| rs181597897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463853 | CTGGCTCTCTTGCTC[A/G]TTTTGGGACCAGTCA | 10533 |
| rs181599321 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447204 | GACACAGTGGCTTAC[C/G]CCTGTAATCCCAGCA | 10533 |
| rs181606939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426362 | GAAATTTATTTTTCC[A/G]TTTTAAAATTATTTT | 10533 |
| rs181613762 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11396744 | CCGAGATGGCGCCAC[C/G]GCACTCCAGCCTGGG | 10533 |
| rs181614278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11505817 | TGCTAGTCAGTGCTC[A/G]CCATTGGTCTTTTGC | 10533 |
| rs181630307 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11468338 | GAGCACAGGCCAGCC[C/G]GCCACTTCCCTGGAA | 10533 |
| rs181637658 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11339811 | ACAAAGCCAAATCAA[A/G]TCACGTGGGTTCTGT | 10533 |
| rs181652142 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11358044 | GAAAAGAAAAAAAAA[C/G]AGGTACTTGGGTAGG | 10533 |
| rs181657130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377369 | TCTGGGCCTGCTGAA[C/T]GGTGGTGTGTGGACC | 10533 |
| rs181695820 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11412563 | TTGTAGCTTTGTACT[A/G]TAGTAAATTTGATTA | 10533 |
| rs181702834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293579 | CTGGCCGGGCGGGGT[A/G]GCTCACATCTGTAAT | 10533 |
| rs181703708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11299772 | GGGCATTGTCCATGG[A/G]CATTGATCAATGAAT | 10533 |
| rs181704508 | snp | C/G | 0.0217236 | 0.101931 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271440 | TTTAGCCGGGATGGT[C/G]TCGATCTCCTGACCT | 10533 |
| rs181719348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314203 | ATAAGTTCATTAGAG[A/T]TGGTTCCCAGAAGAG | 10533 |
| rs181759639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11392230 | AAACATAGTTCATCT[C/T]CCATTTTGGTTAATT | 10533 |
| rs181784870 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11282749 | AGGCTTTAAACCTCC[C/G]TCTTTAACAGCCTTG | 10533 |
| rs181786439 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11430999 | CAAGTCTTTAGTATA[A/T]TACTCAAAATCATGA | 10533 |
| rs181787803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277548 | ACTGTGATGCCGACC[C/T]GAGCTGCAAAACCAG | 10533 |
| rs181796207 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11329223 | ATACACCAAGATGTT[A/C]ATAGTTCTCTCAGGA | 10533 |
| rs181806781 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11369075 | TGCTGAGGTGGAGCT[A/G]GGATCTCTAGCCATA | 10533 |
| rs181814566 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11408016 | TTCTCCTCAGAAAAT[G/T]GGATTTTCTTTTCTA | 10533 |
| rs181848983 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11320174 | CTACCCCTCCCTCCC[C/G]CTACCTCCCCTTTGC | 10533 |
| rs181883174 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ATG7 | GRCh38.p7 | 3:11488621 | CAGCCCGCGGGCCTT[C/T]GAGCCTTCTGGGGCC | 10533 |
| rs181884261 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526839 | AATCTAAAGTTTTAC[C/T]ATTTACCATCATGTT | 10533 |
| rs181888954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11545857 | GCAGAAGAAGTGGGG[A/G]TTAGCACCCCCATAC | 10533 |
| rs181906212 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550183 | CTCAGTGGTATCCTT[C/G]CAAGATCAGAAATTT | 10533 |
| rs181919321 | snp | C/T | | | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272534 | GGGCGAGGGTCACAG[C/T]AAGTCTCAGGATCCT | 10533 |
| rs181940642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314651 | ATGGGTGAATTGGGC[C/T]AGGCACGGTGGCTCA | 10533 |
| rs181949958 | snp | A/G | 0.000749684 | 0.0193463 | intron-variant | ATG7 | GRCh38.p7 | 3:11358400 | TCCAGACATAACTAC[A/G]TCCTGGTGTTTCCCT | 10533 |
| rs181998245 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11472835 | TTGGAATGCCAAATG[C/T]GCTGATTTGCACACC | 10533 |
| rs182007202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532188 | CAACAAGCGTGTATT[C/G]AGTATGATTTCTGAT | 10533 |
| rs182010357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11538399 | CCCAGGACATGGGAC[A/G]AGACAGACCTATGTG | 10533 |
| rs182011668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455696 | CCCCTCAGAGTTAGC[C/G]CGAGCTGGCCACAAC | 10533 |
| rs182018863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11435761 | TGATTAATAATTCCT[A/G]CTCCTCACAATTACC | 10533 |
| rs182019211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516359 | AAATTAAAAAAAAAA[A/T]GATGTTCCACATCAT | 10533 |
| rs182026563 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11418001 | TTTTTTAGTAGAGAC[A/G]GGGGTTTCACTGTGT | 10533 |
| rs182033462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11397581 | TCCTGCCTCAGCCTC[C/T]GAGTAACTGGGACTA | 10533 |
| rs182038081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11305878 | TGGACTTTAAATGAA[A/G]AGACATAGGTTCTTC | 10533 |
| rs182041598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379134 | TGAGCCTGAGGTTTT[C/T]CAACATAAAATGGGG | 10533 |
| rs182041943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11505887 | AAGGTACACAGTGCA[A/G]TGGTAACATCTGGAA | 10533 |
| rs182061640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349260 | GTCCCCACTCAACCC[A/G]GGAAGTCCAGCTGGT | 10533 |
| rs182073534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11388998 | CACACCTGTAATATC[A/G]GCACTGTGGGAGGCT | 10533 |
| rs182081818 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ATG7 | GRCh38.p7 | 3:11525076 | GAGACTGGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 10533 |
| rs182083522 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11491142 | GTCTTTTCACATAGT[C/T]CCATATTTCTTGGAG | 10533 |
| rs182098790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465227 | TTTGGGAGGCCGAGG[C/T]GTGTGGATCCAGATC | 10533 |
| rs182102033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511341 | TCCATGTTCCCATCA[G/T]ATTAGTTAGATACAG | 10533 |
| rs182104619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11448161 | AAGAAGTCTTTATTC[A/G]CTGAGGCTTTGAAAA | 10533 |
| rs182109751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11492576 | GTGCTCAACTCCTCG[C/T]GGGAGGGAGCACGTG | 10533 |
| rs182113283 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11428216 | TAAATTCCTCCATAG[G/T]TTGCATATCCTCACC | 10533 |
| rs182123055 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409266 | AGAAACATATTTCAA[A/G]TTGTGAATTTTGATA | 10533 |
| rs182137109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11389587 | GCCTGTGTGGGCCTT[A/G]AGCTACTGCAAGTGT | 10533 |
| rs182215583 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11293685 | AAACCTGTCTCTACT[A/G]AAAAATACAAAACAT | 10533 |
| rs182225550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427936 | CAATTCCTCAGAATT[A/G]ATGAGTGAGATTAAA | 10533 |
| rs182226244 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11340282 | TAGAGAAGCCTCAGT[A/G]GGGTTATACCTACCC | 10533 |
| rs182242002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350975 | ATCTATCGTTGGAGA[C/G]TATTATGAACTCCCT | 10533 |
| rs182243398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11370380 | GGTGGGAGCTGAAGC[C/T]CTTAGCTGAAACAAA | 10533 |
| rs182285134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11552951 | TATAAAGCCCAGCCC[C/T]GGCCCAGGCCCGAGT | 10533 |
| rs182299661 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11344728 | ATAAAAATTAGCCAG[G/T]CTGTAGTGGCGCGTG | 10533 |
| rs182313607 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558000 | CCTTAAACCCTTTGT[C/T]TTTCAGCAGTTTGCC | 10533 |
| rs182313950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389213 | GCTCCAGCCTGGGGA[A/T]CAGAGAGAGACCCTG | 10533 |
| rs182319332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520342 | AGGCCATTCTCTTCC[A/C]TTAGTTTATTCACTC | 10533 |
| rs182328947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464636 | TAATTATACCATTTA[A/T]TTAAATATCCCCCAA | 10533 |
| rs182353540 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11484950 | GTCTATCGTTGTTGG[A/C]CAGTTGGGTTGGTTC | 10533 |
| rs182357418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421161 | ATTGATGGTGGCCAC[C/T]TGATCAGGGTGGTAG | 10533 |
| rs182370665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11280164 | CAATTCTCAAGCTTC[A/G]GCCTTCCGAGTAGCT | 10533 |
| rs182376580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302646 | GTAATCATTATTTCA[A/G]GAAAACTTATTGATT | 10533 |
| rs182380525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325072 | TATTAAGTATGGTCA[C/G]ATGCTCTCCAGGTTT | 10533 |
| rs182401663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289629 | GTGCAATCATGGATC[A/G]CTGCAGCCTCAACCT | 10533 |
| rs182440796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11550694 | TGCCTGGCCTCTCTT[C/G]TTGATTTCTAAGAGC | 10533 |
| rs182440815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380849 | TTACAATTTGGAACT[A/G]TTTTTCGTGTAGCCT | 10533 |
| rs182449754 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11517023 | GGGAGGTGGAGGTTT[C/T]AGTGAGCTAAGATCG | 10533 |
| rs182467275 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11458191 | ATTTCTTCATTTTTT[C/T]CCTATCTCAGTGGTC | 10533 |
| rs182497181 | snp | C/T | 4.97294e-05 | 0.0049862 | intron-variant | ATG7 | GRCh38.p7 | 3:11307097 | TATGTGTCATATTTC[C/T]TGTGGTCCTGGCAGG | 10533 |
| rs182503411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408787 | TTCAGTAGTCTCCCA[C/T]TGGGTCCTTCCCATA | 10533 |
| rs182586814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11365941 | ATAGAACTTGTGGGC[C/T]GGGCGCGGTGACTCA | 10533 |
| rs182590786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483806 | CCAATCAGGATGGAC[G/T]CTACGGTAGAATTTA | 10533 |
| rs182592216 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11517621 | CTGGCCCTGGGAGGC[G/T]TCACTAGAGGTTTTC | 10533 |
| rs182598331 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11485144 | ACAAGGGTTGAACTA[C/G]TTTGCAGCCCCACCA | 10533 |
| rs182598693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447756 | TTGGCCAGGCCTGGG[C/T]CACATGCCATCTCTG | 10533 |
| rs182601654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11503540 | GAGGTGGGCAGATCA[C/T]GAAGTCAGGAGGTCA | 10533 |
| rs182602053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11439200 | CAGCCTCCCGAGTAG[C/T]AGGGACTACAGGCGC | 10533 |
| rs182607510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11465647 | GCACACACCTGTAGT[C/T]CTAGCTACTTGGAGA | 10533 |
| rs182622712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448793 | TGGGGTGGGTAAGGG[A/G]GTCGCTGTTCCAATA | 10533 |
| rs182625419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444515 | CTTTGTGAAGGCATA[C/G]TGTAAGTTATTTATC | 10533 |
| rs182628590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401569 | GTCAGTCCACTTCAT[A/G]CTCAGCTTTTAACTT | 10533 |
| rs182637234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405941 | GCCATGTGTAGCATT[A/T]CTCTTTCCTTCCTTT | 10533 |
| rs182637396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288522 | CCATTGGGTTAGGAC[C/T]TTTTTCTTTAATTAT | 10533 |
| rs182660829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551259 | GTGGGGGCTTCTCAC[C/T]GCTCTTCTGTTCGGA | 10533 |
| rs182667298 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11360996 | TCACCAATATAAACG[C/T]GGCTACAAACCATAT | 10533 |
| rs182671597 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11534411 | CTTGGAACAGAGGCC[C/G]TCAGCATCTGTCCTC | 10533 |
| rs182672536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532721 | GAGTGAGACCTGTCG[C/T]AAAAAACGAAACAAC | 10533 |
| rs182698623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11474706 | AAACTGGCAGGTTGT[C/T]AGTAAAGGTCCCTCA | 10533 |
| rs182713958 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11503176 | GGCTCTTTGAATGAC[A/G]GTCGGCCAGATGACC | 10533 |
| rs182716433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11538640 | TGAAGCCCAGGAGTT[C/T]GAGACCACCCTGGTC | 10533 |
| rs182736852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284574 | TTTTATTTTTTGAGA[C/G]GGGGTCTTGCTCTGT | 10533 |
| rs182743155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423447 | TGATTCCTTTGCTCA[A/G]TGCGGGGTTGCCACA | 10533 |
| rs182750548 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11405647 | ATTTTTATTTTTGAG[A/T]CAGGATCTCTCACTC | 10533 |
| rs182760897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375305 | TATGTAACAAACTTA[C/T]AATACAGCAATTTAA | 10533 |
| rs182761229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330441 | GTTGCACAAATTGTT[C/T]CAGCCTTGGCTATTG | 10533 |
| rs182767636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385922 | TAATTTTGGCCATCC[G/T]TGGAGTTGGAATCTG | 10533 |
| rs182768574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11394527 | AAAGGAAGTTGAGAG[C/T]GTGAGCCACACCTTT | 10533 |
| rs182812709 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11506504 | GGGCAGATCACTTGA[G/T]GTCAGGAGTTTGAGA | 10533 |
| rs182813937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11461417 | GCTTAGAATTTCCAC[A/G]GCGTCTTTTCTTCCC | 10533 |
| rs182814865 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11289760 | AAATGGGGTCTCACC[A/G]TGTTGCCCAGGCTCG | 10533 |
| rs182815616 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11521181 | CAGATCAGTAGAGCC[A/C]TAGGCAGCCATTGGT | 10533 |
| rs182818332 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11488711 | AGGTTACATTTATTG[A/G]TTTGCATATATTGAA | 10533 |
| rs182826116 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11445068 | TAGATGCTGGCGAGG[C/T]TGTGGTGAAAAAGGA | 10533 |
| rs182829250 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469694 | CAGGCTATTAGAGAT[A/G]GTGTACTGGGGCCAA | 10533 |
| rs182829276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325337 | TTACTATTTGTTAAG[C/T]GCTGGCCTCATTCTC | 10533 |
| rs182829330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11424258 | CAAAAACCAACTAAA[A/G]ATTTTAGTATTTTTA | 10533 |
| rs182831579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11311560 | TGAGCTGAGATCGTC[A/G]TGCCGTTGCACTCCA | 10533 |
| rs182834693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338118 | TCCTCCCACCCTTCA[C/T]CCTCAAGTAGGCCCC | 10533 |
| rs182835413 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345181 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 10533 |
| rs182841572 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406193 | TGGGGTTTCATCATA[G/T]TGCCAAGGCTGGTCT | 10533 |
| rs182842425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356430 | TAAACTCTCTAGGTG[C/G]TTCTGATATACAGCC | 10533 |
| rs182848344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11366534 | TATGCTGTCGTATCT[C/T]ATTTGAATCTTTCCC | 10533 |
| rs182875590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11385054 | TGTTTGTTTTGGGAC[A/G]GAGTCTTGCTCACTT | 10533 |
| rs182887425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11359103 | TATACCAATTATGTT[C/T]ATATATAAACATTGA | 10533 |
| rs182893616 | snp | A/G/T | 0.00756178 | 0.0610554 | intron-variant | ATG7 | GRCh38.p7 | 3:11379887 | TATTAATCATTTCCT[A/G/T]CTTGTTGTCAGAAAC | 10533 |
| rs182910361 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11423556 | GACATTTTTTCCTGA[C/T]GTAACATTCTGGTTT | 10533 |
| rs182916664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553828 | ACTTTGAAAGCCAAG[C/T]TGGTGTTGATATTTA | 10533 |
| rs182937598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11473860 | TGTGCTGTGCTCAGA[C/G]TTCTGTTGAACCCCA | 10533 |
| rs182944849 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419391 | AAACCCCATCTCTAC[A/T]AACAATACAAAAATT | 10533 |
| rs182952530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399451 | CAGGCAGATTTAGGT[A/G]AAAAATTATGAGGAA | 10533 |
| rs182954186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296213 | CAGTATCCATGTCCA[C/G]TTTTCTTGGCTTATC | 10533 |
| rs182955849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11315653 | CCTCTCCCACCCCTA[C/T]AGTTATCGAATCAGC | 10533 |
| rs182960992 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11341199 | CCTGAGTAGCTGGGA[G/T]TACAGGCACGCGCCA | 10533 |
| rs182970143 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11285363 | TTATTTTTTGTAGAG[A/G]TGGGGGCCCACCGTG | 10533 |
| rs183043402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529814 | GTTGATGTCTCTGCC[C/T]GAAGGTACCAAGGAT | 10533 |
| rs183043644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11499059 | TTCCATTTATTAAGT[A/G]GTTAGGACCAAACAA | 10533 |
| rs183154882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530354 | CGTACTCCGAGAAGC[A/C]CTCTGCATCGCCACC | 10533 |
| rs183155986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11490248 | GGCCTTGTCTCTTTT[A/G]ATCTTTGTTGGTTTA | 10533 |
| rs183157349 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11529307 | AGATCATTGATTGGG[A/T]GGAAAAATCCAATAA | 10533 |
| rs183160511 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508186 | TTCACTCTTACTAGC[A/T]ATGGACAGGCCCCTA | 10533 |
| rs183161983 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311457 | AAAATTAAAAAAAAA[A/T]ATTAGCTGTGCATGG | 10533 |
| rs183164463 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11470702 | TGTGTGGGCTGACAT[A/C]ATGTGAGGGCCACAG | 10533 |
| rs183165656 | snp | C/G/T | 0.00954224 | 0.0684493 | intron-variant | ATG7 | GRCh38.p7 | 3:11548687 | CCGGAACTGAGCCCC[C/G/T]GTATCAGCCGATTGA | 10533 |
| rs183173345 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11513387 | TCCTGAGCCCTGCCC[C/T]GCGGGGAGGCAGCTA | 10533 |
| rs183177305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454642 | CATTTCCCTTTTAGC[C/T]TGAGTAAATAAAGGT | 10533 |
| rs183182363 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11434040 | ATATGAAAAACATTA[C/T]GGTCATGTGATATGA | 10533 |
| rs183188492 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11416075 | CCTCCTTGACTGAAA[C/T]GTCATGTGGTGCATT | 10533 |
| rs183197921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11355942 | CAAATCACCATCAAC[A/G]AGAGAATCGATAAAT | 10533 |
| rs183201219 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11492034 | ACCTAAGCAAGCCTT[G/T]GCAATGGTGGGCGCC | 10533 |
| rs183214332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394088 | AAATCGTTGTCCAGG[G/T]TCATAGAATGAGTAA | 10533 |
| rs183224111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11432189 | AGTGAGTGAAAATGA[C/T]TGGTTGGCGTTGGAG | 10533 |
| rs183225765 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11428810 | TATTGTTAGCTAGAA[G/T]AATTTCAACCTGAAA | 10533 |
| rs183228169 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11547179 | TGTTTAACAGGAAGT[A/G]GTGAGAGAAAGTGGA | 10533 |
| rs183229118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283800 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 10533 |
| rs183237337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453382 | TAGAAAACTCAGAGG[G/T]ATAAAAGGATATGCT | 10533 |
| rs183247415 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415486 | CACCTAGCTTAAAAC[A/T]CAAATTGTACAGCCA | 10533 |
| rs183253022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329824 | ACTATTAACTCAGCT[C/T]TAGACATTTCCGATT | 10533 |
| rs183279107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11510936 | AAGCCGCGGACCCTC[A/G]CGGTGAGTGTTACAG | 10533 |
| rs183291939 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11548305 | GTCTCTTATCAGATA[A/C]ATGATGTGCAATTAT | 10533 |
| rs183299526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514343 | AACTTTGAAGATGGG[C/T]GTTTGCAATTCATTT | 10533 |
| rs183324053 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11489423 | TATTGATCCTTTCAA[A/G]AAAACCAGCTCCTGG | 10533 |
| rs183328225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11302382 | CCTGATTTCTTTATT[C/T]CAAATTATTTCCTTT | 10533 |
| rs183356406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344606 | GCACGGTGGCTCACA[C/T]CTGCAATCCCAGCAG | 10533 |
| rs183368503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11383694 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 10533 |
| rs183370517 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11401140 | TCAGACCCCGCCCCA[G/T]ACCTAATTAATCAGA | 10533 |
| rs183372613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414144 | CTTGGCTCACTGTAA[C/G]CTCCACCTCCTCCCA | 10533 |
| rs183374678 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11552032 | GGGATTACAGGCGTG[C/T]GCCACCACGCCCGGC | 10533 |
| rs183390624 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535790 | TTCCCAAGAGCCCTC[G/T]GGGGCATTTCAGAAC | 10533 |
| rs183417777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11492322 | CGCCCTGCTTCGGCT[C/T]GCACACGGTGCTCTG | 10533 |
| rs183427022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337602 | TTTTTTCATTATTAA[A/G]TTTAAAGGGCATCTA | 10533 |
| rs183427148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479787 | GGTTTTTAATAAACC[C/T]AGCTAACCTCCCTCC | 10533 |
| rs183429017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11474225 | GACAAGGCAGGGCCT[C/T]TGTTTTCATGGAGCC | 10533 |
| rs183432336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11457661 | AGGCACAAAGTGACT[A/G]TACTAGTTAAGGGGT | 10533 |
| rs183437828 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11303782 | CTTTATTCATAAGAA[A/G]TTTTCTTTTCGGCCG | 10533 |
| rs183439115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11331240 | TAATTTTTAAGGCTT[C/T]GCAGAAAGCATAAAA | 10533 |
| rs183441289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11437853 | AAGAATATAGACATT[C/T]TCTGATGTAAACAGA | 10533 |
| rs183442155 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373863 | GCAGAGCATATGAAT[A/G]GTGGCAAGTCAGAGT | 10533 |
| rs183449037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11452449 | GTGATGGTTTACACA[A/G]CTGTGAACATATTAA | 10533 |
| rs183449534 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11420729 | TGTCTAAAAATACAT[A/G]CATACCTTAAGTAAT | 10533 |
| rs183459114 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11371161 | CCATTCTCTGGGGTA[C/T]CATTTTCCACATTAT | 10533 |
| rs183476562 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433019 | CATTTGGGATGGGTA[C/T]AGTGGCTTACACCTG | 10533 |
| rs183491431 | snp | A/T | 0.00407746 | 0.0449678 | intron-variant | ATG7 | GRCh38.p7 | 3:11410330 | TGTGAATGATATTGT[A/T]TTTTTTTTTAAATTA | 10533 |
| rs183499949 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11437029 | AAAACCATTGAATTC[A/T]ATACTCTGAATGGAT | 10533 |
| rs183502625 | snp | A/G | 0.499853 | 0.008585 | intron-variant | ATG7 | GRCh38.p7 | 3:11485895 | TGTTCTGTTCCATTG[A/G]TCTATATCTCTGTTT | 10533 |
| rs183514612 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466613 | AAGTTCCATTATTTA[C/T]AACAGGTTTCTTAAA | 10533 |
| rs183516264 | snp | C/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450474 | CAGTTTATAAAGATT[C/G]TCTGGGACTAACTCC | 10533 |
| rs183523702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372003 | TAAAGCGAGGCCAAA[C/T]GACCTATTCTGATGC | 10533 |
| rs183528113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430462 | AAAGGTCTCCACTTA[C/T]TTATTTTAGCAACAC | 10533 |
| rs183531338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11391245 | GCAAGTTTTTAGATT[C/G]TTTTTCTTTTTCTTT | 10533 |
| rs183531664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411317 | TTTAGAATTACCTGT[A/G]TGTTCTGTATATTAA | 10533 |
| rs183539232 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349735 | GTGTTATTTTTCCTC[C/T]ATCACCAGGATACTT | 10533 |
| rs183545026 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11369767 | TTGTCCCAGGAGGAG[G/T]TGGGCCTAACCTTAC | 10533 |
| rs183545671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11539201 | TCTGAGCACTTTATG[C/T]CCACTAACTCATTTC | 10533 |
| rs183553501 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11507231 | AAGTTTCAGTGAGCT[A/G]AGATCACACCACTGC | 10533 |
| rs183562814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470227 | GTCACACATCACTTA[A/G]CGATGGGGATGCATT | 10533 |
| rs183580870 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11323009 | AAGGCTGAGGCAGGA[A/T]GATTCCTTGAGCCCA | 10533 |
| rs183599020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11365613 | CTATCTGGTGATTTG[C/T]AAGGACAGACTCAGA | 10533 |
| rs183621982 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390430 | CTATTTTTGATAATA[A/T]TCCAATAGGCGCTGA | 10533 |
| rs183632321 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11281761 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 10533 |
| rs183644244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11326947 | GTTGAGAAAGGAAAG[A/G]AGGAAGGAAAAGGAA | 10533 |
| rs183645837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11304983 | TCCCAAAAAAGACAC[C/T]CTTAGCAATTACTCT | 10533 |
| rs183648968 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11376337 | ATGGTATGTGAATTA[C/T]ATCTCAAACCCGTTA | 10533 |
| rs183657304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11394948 | GCAAAGACAAAAGAA[A/G]TACAGACATACAGAG | 10533 |
| rs183658016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341825 | CTAGGAAAAACTTTC[C/T]TCTTAATCAGATGGT | 10533 |
| rs183665301 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279481 | ACAAGGTCAGGAGTT[C/T]GAGACCAACCTGACC | 10533 |
| rs183678663 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11275104 | TTGAGAGATTAAGGA[A/G]GTGGAATTTGCTGGA | 10533 |
| rs183687321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307751 | GGGGGCAGTTTATCC[C/T]AATCCTGTCTAACCG | 10533 |
| rs183695367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11351798 | AAACTATTTAACTTA[C/T]TGGTTAGCCAGCCTT | 10533 |
| rs183710157 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390094 | GTTGAAACCTCCTAC[A/G]TATCCCAAATGTGGA | 10533 |
| rs183717675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298038 | CAAAAAATTAGCTGG[A/G]CGTGGTGGCATGCGC | 10533 |
| rs183720773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275638 | GCTGAGATTACAGGC[A/G]TGAGCCACCGCTTCC | 10533 |
| rs183725335 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11456810 | GTCACATTTTTTCGC[A/G]TTCACACTGTATGTG | 10533 |
| rs183735278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318745 | CCCAAGATACATCCT[G/T]TGCTCTGGCTACCCC | 10533 |
| rs183744975 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11274863 | AGGCCCAGAAGTTTG[G/T]ACTCTAAAATGTGGG | 10533 |
| rs183799165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11478509 | GGATTTGGAATCTGG[A/G]GTTCCAGAGAGCACG | 10533 |
| rs183837004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552607 | ATGGGACGAAGCCAG[G/T]GGAGAGCCCGTCCCT | 10533 |
| rs183843977 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11539416 | ATGGCTATAGCAGAA[G/T]CAGATCAGGGTAAGA | 10533 |
| rs183884186 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ATG7 | GRCh38.p7 | 3:11546197 | TTTTTTTTGAGATGG[A/T]GTCCTGCTCTGTCAC | 10533 |
| rs183897051 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527035 | TATATATGTGTGTGT[A/G]TATATATGTGTGTGT | 10533 |
| rs183916518 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11504304 | GTATCAAGCCAAACC[A/G/T]CTCATTGAATATGAA | 10533 |
| rs183920623 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11511932 | CCCAGAACTCCAGCT[A/G]GCCTGCAAGCGCCGC | 10533 |
| rs183932091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11524192 | TTGTCTACCTGGCAG[C/G]CTCCCCTTCACTAGC | 10533 |
| rs183947435 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11537525 | ACTTCCTTCATAGAG[C/T]CCCATTTTCCTTCCT | 10533 |
| rs183960535 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11505417 | GTTGTTTAGAATTGA[A/G]GACATGGACCTTTTG | 10533 |
| rs183966825 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11518447 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATCT | 10533 |
| rs183969252 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11486422 | AAGTTGCTTATCAGC[A/T]TAAGGAGATTTTGGG | 10533 |
| rs183974675 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11498267 | CCCCTATTAGAATTC[C/T]AAAACAGCAATCTTC | 10533 |
| rs183981537 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11468270 | CCCGAGGAATCTGCA[A/G]TCTCTGCGTAAGTGA | 10533 |
| rs183988390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522444 | GACACTGGGGAATTC[C/T]GGAATAAGCTCACGA | 10533 |
| rs183992802 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11539806 | GTACTCGCTTGTGGA[A/G]CCAGCACAGTTCGGC | 10533 |
| rs183995997 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508938 | TCTCTGCTCCTGTTA[A/C]CAATGACCAATATTC | 10533 |
| rs183998140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460577 | TTTTCCCTCAGAGTA[C/T]TTCCCATTCAAGAGG | 10533 |
| rs184002854 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481043 | TGGAAAAAATGTACT[C/T]CCTTTAATGTCTTAT | 10533 |
| rs184003189 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11463709 | TTCTCTCCCTGCAGA[C/G]TGGCGTCTTCTGCTA | 10533 |
| rs184016720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11554626 | CAGGTGGTTCACACA[C/T]TAGTGACGCCTTGGC | 10533 |
| rs184020312 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490631 | TTCCTTTCCATGTTT[A/C]GTGGTTCCTTCAGGA | 10533 |
| rs184020385 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446685 | GACTTTTGACTTCTT[C/T]CTGTAAGATGCTACC | 10533 |
| rs184023318 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ATG7 | GRCh38.p7 | 3:11426064 | GCTATCATGAATAGC[A/G]CTGCTGTGGACACTT | 10533 |
| rs184031140 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11407759 | ATGAACTCTGTGTTG[A/G]CCCCTTTCAGCCACA | 10533 |
| rs184047894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521910 | ACTCTAGACTGCCGC[C/T]GCTGCCGACAACAAT | 10533 |
| rs184063041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555754 | GTGAGGCCCCAACCC[A/G]GGAGAGGCCATGGCC | 10533 |
| rs184064464 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11517930 | ACTTCAGAAAGATGG[A/G]CACAGTGTGAGGGAT | 10533 |
| rs184069728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317284 | CTAGTGTGAAGTCCT[C/G]TTGTCATAGCAGGCA | 10533 |
| rs184082899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360472 | TTATAATCTAATTAC[A/C]CTTACATGCAAAAAA | 10533 |
| rs184083760 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11541941 | ATATCTTGAAAGAAA[C/G]CATGTGGGTGCCACA | 10533 |
| rs184087841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439866 | CTGTGATTTTCAGGG[C/T]GCTTTTGTACCTGCC | 10533 |
| rs184097772 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11485643 | CTGAATGGTAATGCC[G/T]AGGTTTTCTTCTAGG | 10533 |
| rs184102440 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11421731 | GCTTTGATCAGATCC[A/G]TCAGAGAAATCACCC | 10533 |
| rs184108708 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11402845 | GTTTATTTAACAATC[A/G]ACGTCAACAATTACC | 10533 |
| rs184115899 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382320 | ACGCACGCACGCGAG[C/G/T]GAGAGCTTTTTATGT | 10533 |
| rs184158956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11458640 | ACTTCTCCATGCTGG[A/G]ACTCAGTTCCCTCTA | 10533 |
| rs184165207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11309266 | TTCACCCCTATGGAT[C/T]ATACTGGCAGTAATT | 10533 |
| rs184191900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11353546 | TGTTGAATTGTGATC[C/T]TCACTGTTGGAGGTG | 10533 |
| rs184210280 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11297378 | CCCATTTACAGTGAC[G/T]GTTCATATGTTCTGC | 10533 |
| rs184219143 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11341303 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 10533 |
| rs184241010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380214 | TTTCATGGATCTGTA[C/T]TCATTCTCACAGTGG | 10533 |
| rs184302499 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286844 | TCCTGAGCTCAAGCT[A/G]TCCTCCCGCCTCAGA | 10533 |
| rs184304336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505106 | ATAGTATGGAAGCTG[A/G]GAGCCTGTTAATTTT | 10533 |
| rs184308963 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334103 | GTCAAAGTCAGAGCA[C/T]GATGTCTGGCACATC | 10533 |
| rs184320709 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270749 | GAGACTATAAAAGAA[A/C/G]CTTCTTAAGGGTGGG | 10533 |
| rs184329571 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11291487 | GCTCTACCACTTCCT[C/G]TGTGACTCTGGGCAA | 10533 |
| rs184338612 | snp | G/T | 5.14011e-05 | 0.00506931 | intron-variant | ATG7 | GRCh38.p7 | 3:11313465 | AATTGGGTTGAATGT[G/T]CAAGAGTAGTTATGT | 10533 |
| rs184359972 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11290660 | ACCAGGAACCACTAT[C/G]TGCAATTAATATACA | 10533 |
| rs184373271 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11339010 | ACAAAGAAAACCAGT[A/G]TACAGGCCGGGCGTG | 10533 |
| rs184397268 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11515346 | TCTCGCTCTGTTGCC[A/T]AGGCTGGAGTGCAGT | 10533 |
| rs184405404 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11480155 | CCAGCATGGTCTCGA[A/T]CTCCTGACCTCGAGA | 10533 |
| rs184406801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293591 | GGTGGCTCACATCTG[C/T]AATCCCAGCACTTTG | 10533 |
| rs184408344 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11500371 | AAAAATTGATCATAT[C/T]GAGTAGGACACCAAG | 10533 |
| rs184410773 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11314393 | GCTGTTCAGGGAGCA[A/G]CCATTATTGATTAAA | 10533 |
| rs184414363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339998 | TAGGACACACTTTGG[A/G]AACTGCTAGAATTGG | 10533 |
| rs184414578 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11435204 | GCTACCATTGCCAGA[A/G/T]ACAACTTTTTGCAGA | 10533 |
| rs184424776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417586 | TTTCTTTTAGATACC[A/G]TATAATTGGGTTTTA | 10533 |
| rs184426069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11462593 | TACCTGGCCCTGGGA[C/T]GATGAAAGCAGAGGA | 10533 |
| rs184426270 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11445392 | AAAGAAGATCATGGA[G/T]GGAGCTGGAGGCCTT | 10533 |
| rs184428106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358113 | CTGGAAAGAGCCAAA[A/G]ATACACAGTTTTCTC | 10533 |
| rs184432734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397155 | CCAGATTTTTAAATT[G/T]ATATGCATTATACAA | 10533 |
| rs184435812 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11378053 | TTTTTTTTGAGATGG[A/T]GTCTTACTCTGTCAC | 10533 |
| rs184480872 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11495451 | AAGGAGACAGGCTGG[C/G]AGAGACCCCCAGACA | 10533 |
| rs184482621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312788 | GATTGTGAAGAGAAT[C/G]GTAACTGTTTGGAAG | 10533 |
| rs184486952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552332 | GTGGCAGTGTTTTGC[C/T]ATACCCTTGTCGGCA | 10533 |
| rs184506250 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11356697 | AACATGCTTTGTCAA[C/T]TGTAGTATGTCAGTA | 10533 |
| rs184553075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11319576 | AATTCAATTTTCTCT[C/T]ACCGGCCTGAACCTC | 10533 |
| rs184568165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342603 | CTGATATTTATTTGT[A/G]TTTATAAAGATTAGA | 10533 |
| rs184574765 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11361315 | TTTGAGACAGAGTTT[C/T]GCCCTGTCACCCAGG | 10533 |
| rs184608981 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11536716 | CCCTGCGGCTCCGAC[C/T]GGGGCCGAGCAGCGA | 10533 |
| rs184629297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477023 | TTCCGATGGCAGTCA[C/T]TAAATGATTGTTATG | 10533 |
| rs184646570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11475841 | TTCTTAACTTTGGTT[C/T]GTCTATGTCCATCTC | 10533 |
| rs184662998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11368208 | GTTGTTCCTTCTTCC[C/T]ATCAACAGTGTTCTT | 10533 |
| rs184663121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411729 | ATGTTGTCCATCTAT[G/T]AAATTCAGTCTATTT | 10533 |
| rs184713311 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11544210 | CAGGTCCCCATGCTG[C/T]GATGGGGCTCCGGGC | 10533 |
| rs184717783 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372571 | GATACAGAATTTTTC[C/T]GTCACCCCAAAAAGC | 10533 |
| rs184756423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451258 | ACTCTGTCACCCAGG[C/T]TGGAGTGTAGTGGCA | 10533 |
| rs184756491 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11511615 | TCCTCAGCCCTTGGG[C/T]GGTCGATGGGACTGG | 10533 |
| rs184779941 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11501752 | TGGAGTGCAGTGGTG[C/T]GATTGTGGCTCACTG | 10533 |
| rs184795437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371741 | ATCACCTGGGACAAA[A/G]TACTTAAGTCCTTAA | 10533 |
| rs184802139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11430615 | ATACGTGTTTAAAAA[A/G]TATACTGAACATCTT | 10533 |
| rs184803217 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11390490 | ATCCTATCCCACTCA[A/G]CAGAAGGACTGCAGT | 10533 |
| rs184809348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458330 | GTGCAGCGGCACCAT[C/G]TCCGCTCACTGCAAG | 10533 |
| rs184816318 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471219 | CAGCTCTTCAGCATG[G/T]CAGCGGCAGACAGCT | 10533 |
| rs184846451 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353940 | TGAGCACCCTTTACC[C/T]TGCTTCTTCTGGGTG | 10533 |
| rs184847587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286059 | TGGGTTTATCTGATG[C/T]TTCCTCCCATGAGAT | 10533 |
| rs184855658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308284 | TCTTATCTACAAAAA[C/T]ATCTTGTGATCCACA | 10533 |
| rs184858524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392013 | GAGGACTTAATTGGT[G/T]AGGCTCCTTCAGGCT | 10533 |
| rs184867568 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11525421 | ATGATTAACTTTACT[C/T]ATAAGAGGTTCACAG | 10533 |
| rs184869175 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11548795 | GGGCCTCTTGGGCCT[A/G]TTCCCAGTCTTTTCC | 10533 |
| rs184869364 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11509664 | CCCCTCCCCCAATCT[A/C]TCTCTAATTTTAAGA | 10533 |
| rs184870994 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11333644 | TATGTGTGTGTGTGT[A/G]TATATATATATACAC | 10533 |
| rs184874274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11530735 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGT | 10533 |
| rs184875405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11352643 | GGCCACGGAGAAAAG[A/G]CTTGACCTAAGTAAA | 10533 |
| rs184877739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11493419 | AAAAGGCAACATTCA[A/G]TTGGTAAAAAGACAT | 10533 |
| rs184882372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362947 | AGTTTGCTAGTAGGA[A/G]ATGAGTATTTAAACA | 10533 |
| rs184887933 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11530574 | CTTGATGGTGAAATG[A/C]ATCCCCTCCTCTGAG | 10533 |
| rs184888896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357844 | GTGAGACCTATCTCT[A/C]CTAAAAATTAAAAAA | 10533 |
| rs184915249 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11511782 | GAAATCGAGCACAGC[A/G]CCGGTGGGCTGGTAC | 10533 |
| rs184926141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280781 | TTCCCCCTGCTCTTA[A/G]CCCCAGCACAGGGTT | 10533 |
| rs184930303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434921 | CAGTGTTCTCATGAG[G/T]GACCTTGGATGAATC | 10533 |
| rs184933131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454949 | AGCTCTATTTTTGAG[A/G]GTTTTTAAAATATTA | 10533 |
| rs184937901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11494879 | GAGTTCGAGACCAGC[C/T]TGACCAACATGGTGA | 10533 |
| rs184943837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11476202 | TTTGCTTTGGTTCTG[A/G]CTTTTTCTTTTCCTT | 10533 |
| rs184945434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11458565 | ACTGCGCCTGGCCTA[A/G]ATTTGGGTTTTACTT | 10533 |
| rs184953526 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11441149 | CTAGCTTTCAAGCAT[C/T]TGTGTTTATCCTACC | 10533 |
| rs184954736 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11278532 | GTTCTTTCATTGTTT[C/G]AGTCATCAACAAGTA | 10533 |
| rs184962741 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11301287 | GGGCCTTTAAGATTA[C/T]TGAGAATTGAAAAAG | 10533 |
| rs184966918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11320910 | GTCTGGTTAAGGCCA[C/T]GTATTTTACAAAGAC | 10533 |
| rs184967751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548897 | AAAGTGAGACGGCCG[A/G]GTCAAAAGTTAAGCC | 10533 |
| rs184971344 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11343979 | TAGATCATCTTTGTT[C/T]TTCAGTAGCATTTTC | 10533 |
| rs184971907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515820 | ATAAGACAATGAATT[A/C]TCTTGCTGGGCTAAA | 10533 |
| rs184988770 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11339553 | CAGAGGTCCTGAGAT[A/G]TAGGGAGCGCAAGAG | 10533 |
| rs185001249 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11376982 | CTGACCTCATCATCC[A/G]CCCTCCTCGGCCTCC | 10533 |
| rs185001466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11526016 | AAACTGTTCAGTGCT[A/G]TGCTGATATAAATGT | 10533 |
| rs185036278 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271820 | TTGTGAAAGGCCTTA[C/G]AGGCCAGACAGAGAA | 10533 |
| rs185036481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11455316 | ATGTCCTTACCCAGT[A/G]AGACTAGCACTTGCC | 10533 |
| rs185042503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11346586 | GTGTGTGCAAATACA[C/T]CTGCATGTGACTAAC | 10533 |
| rs185048238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416780 | CTTGTTACCTAAGGT[G/T]TAAGATCAGATGATT | 10533 |
| rs185055054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386703 | CCAGGTTCTCTTTTC[C/T]TATCTCATTTACCCA | 10533 |
| rs185062430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422396 | ATGGAGACAGCTTCT[G/T]TCCTTAAACCTCATT | 10533 |
| rs185068718 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11425049 | CTAGTTGCAGCCTCA[A/G]CCTCCTGAGTTCAGG | 10533 |
| rs185092280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406615 | ATACCCAAGACTGGG[C/T]AGTTTACAAAAGAAG | 10533 |
| rs185110618 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304528 | TGGGCATGTGAAGCT[A/G]TGTGCGAAGTAGATT | 10533 |
| rs185142740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472475 | GTCGGATCTGGGATA[C/T]ATTCTTATCTCTAGG | 10533 |
| rs185142844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326053 | GAGCCTGAAGAAATC[C/T]TTTGAGATGAAAGGT | 10533 |
| rs185148257 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11393641 | ATGGCTCACCATGGG[A/G]CAGAGAAGAGAGAAG | 10533 |
| rs185154708 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11366657 | CCCCTGCACTGGTTT[C/G]CTTCTTTAAGTCCTT | 10533 |
| rs185170260 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11413637 | AAAGTCAACACAGTT[C/T]ACTGTTATTTCATTG | 10533 |
| rs185192580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298965 | TCTTTTATAATCAGT[C/G]CTCTTCACTAGTTTC | 10533 |
| rs185214517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11335299 | TCGCAGGGGTGTCCA[A/G]TCTTTTGGCTTCCTT | 10533 |
| rs185227670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281310 | GTCTTGAGCTAATCT[A/C]ATCAGTATATTACAA | 10533 |
| rs185235865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11547489 | CTACTGTGTTTGTGT[A/G]CAAGTTTTTATGTGG | 10533 |
| rs185271223 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557733 | GCTATTTTTTCTCCA[C/T]TAAAACATGCATCAC | 10533 |
| rs185288163 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11277440 | TTCTTTCTATTTTCC[A/G]TAAGTGTCAGCTGGC | 10533 |
| rs185298004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522893 | ATCTAGAACAAACGT[A/G]TCTGAGGTCAGGTCC | 10533 |
| rs185309819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490972 | TGCTCTTCTTGAGGA[A/G]TATCTTTGTGGTGTT | 10533 |
| rs185368435 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11404893 | TCAGTTACCTCCTAT[G/T]GGGTCCCTCCCACAA | 10533 |
| rs185427128 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ATG7 | GRCh38.p7 | 3:11488645 | TGGGGCCTCCGGCGC[C/T]GTGACCTCCTCTCAA | 10533 |
| rs185433129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11506083 | TTCAGTTAGTGAGTT[C/T]GTGTATTTTTTGAGT | 10533 |
| rs185436111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469317 | AGCCAGGCGTAGTGG[C/T]GCATGCCTGTGATCC | 10533 |
| rs185438251 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11509413 | TTTTTTTTTTTAAGT[A/G]CCAAATTGTGAGCTC | 10533 |
| rs185440903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11344355 | CTCTTGTTTTTATCT[C/T]TAATTTTGATGTTGG | 10533 |
| rs185449450 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11364568 | GGCATTTTAGTTATC[C/G]TTATGAATCTTATGT | 10533 |
| rs185451208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458866 | GCAAGCGAGCATTAA[C/T]GCCTGTGCTCTGCCT | 10533 |
| rs185454339 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11452190 | AGGCATTCAAGACCA[A/G]CCTGGCCAACACAGT | 10533 |
| rs185457489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11442836 | TGAGATGGGAAGATT[A/G]CTAGAGCCCAGGAGT | 10533 |
| rs185459651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383456 | CTTTCGGTGATGCTA[A/G]TTTTCCCTTTTCCAT | 10533 |
| rs185460284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11431866 | TATATTTATATAGAA[A/G]GGGGCACATAGTAAT | 10533 |
| rs185461718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423217 | GCCAGTTGGTGAATC[C/G]GTCAGAACACATACT | 10533 |
| rs185465142 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334980 | AAAAAAAAAAAATCT[C/T]TTCTGAGATATCTTT | 10533 |
| rs185465151 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11445912 | TGTTAAACGTCTTAT[G/T]TATATTACTTATTTG | 10533 |
| rs185485840 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11407078 | GTCCCTTCTGCCTAT[G/T]AGCCTATATAAATCA | 10533 |
| rs185522601 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11521277 | CCATACGTGCTAGAT[A/C/G]CTGACAAAGACCAGG | 10533 |
| rs185526871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553581 | CCGCACTGAGGATGA[A/G]CTCGGTGGGGACCTG | 10533 |
| rs185528677 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538724 | AGCCAAAAAAAAAAA[A/G]AAAGCCAGATGTGGT | 10533 |
| rs185532784 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11506716 | CACTGCACTCCAGCC[C/G/T]GAGTGGCAGAGCGAG | 10533 |
| rs185535419 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558139 | GACCGAACCAAACAC[A/G]CCGTGGAAGCTGAGC | 10533 |
| rs185538780 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515516 | GCTGTGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 10533 |
| rs185542419 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11480394 | CATTTAAGATTGGCT[A/G]GGCGTGGTTGTGCAT | 10533 |
| rs185555503 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11488721 | TATTGATTTGCATAT[A/G]TTGAACCAGCCTTGC | 10533 |
| rs185588252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295933 | ACAGGCATGTGCCAC[C/T]ACACCCAGCTAATTT | 10533 |
| rs185591358 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11462953 | TGTAATGGTGCGATC[G/T]CTGCTCACTGCAACC | 10533 |
| rs185592392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273726 | TGATCTATCAGTAAA[A/G]TAAGAAGAAAAAGAA | 10533 |
| rs185592473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348195 | CTCATCTCAGAGAGG[G/T]ATAAAAAAACACAAC | 10533 |
| rs185602601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368855 | TTCACATCTTTTGTC[C/T]TTAGGTGAATGAACT | 10533 |
| rs185607519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315037 | GATTCATGTTGGGTT[A/G]TCATAGGAGAGAAAG | 10533 |
| rs185609978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11425334 | CTTTATCATTATGAA[A/G]TCTTAAAAGTGGAAT | 10533 |
| rs185611846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340934 | AAGGGCACACTCTTC[A/G]TCTGTTCTAGACATT | 10533 |
| rs185613541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11388595 | CACCACGCCTGGCTA[A/G]TTCTTTGTACTTTTA | 10533 |
| rs185649058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387194 | ACAGGTATAATGGGA[A/G]GGATTGAATCAGGGA | 10533 |
| rs185655668 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11320324 | GAGTTTCACTCTTTG[C/T]TGCCCAGGCTGGAGT | 10533 |
| rs185667440 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11501158 | ACCTGGGATGCTGAG[G/T]TGGGAGGATCACTTG | 10533 |
| rs185671979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362101 | ATTTAGTGATTGTCA[A/G]CAAATACGATTAGTG | 10533 |
| rs185707005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379908 | TGTCAGAAACCAGAC[A/G]TGCATTTCATAGATG | 10533 |
| rs185708001 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11466060 | AGCATTTTCTGGCTC[A/C]GTTTTAGAACCTAAA | 10533 |
| rs185714595 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11403504 | TAAAGGATGAAAAGA[C/T]ATCATTTAAGAAATG | 10533 |
| rs185720568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429617 | CAAGAAGCAAAGTTT[A/C]TAGATAATGCACTTG | 10533 |
| rs185721888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11400417 | CAACAGAAAATAAAT[A/G]GGGACTGTGGCCAAC | 10533 |
| rs185732617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11277867 | ACTGCGTAAGACAGA[C/T]ACTCCCAGAGCGGCC | 10533 |
| rs185762985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523691 | GAGCAAGCAACAAAG[C/G]TTTTAAAATGTCGGC | 10533 |
| rs185765159 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11383072 | ATATCCTTATCAAAT[G/T]CAGGCAATTTAATGT | 10533 |
| rs185772378 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11503187 | TGACAGTCGGCCAGA[G/T]GACCCTATACTGAAG | 10533 |
| rs185773010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11355308 | AAAGTTTCGAGGGGA[A/G]AGCATCTTAGTGGTC | 10533 |
| rs185782978 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11544490 | TCCCTGTGGCCTCTG[A/G]CCCAGAGCCAACCCA | 10533 |
| rs185783826 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11509931 | AGTGATCTTGGATGG[A/G]TGATATAAATAGACT | 10533 |
| rs185802663 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11343608 | TCTTTTCCTTTGTGG[G/T]TTATGGAACTCTTGT | 10533 |
| rs185817569 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382599 | AAAGACCTTATTTGA[C/T]GTTTATATGAGTTGC | 10533 |
| rs185829330 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11423096 | GTGAGAAATGTGTGA[C/T]TCTTCCTTTCACTTG | 10533 |
| rs185848756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11449776 | CAAACACTAACAGGC[A/G]CTTTGCCATAGTACT | 10533 |
| rs185849620 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11311138 | CTTGCTGCCTTGTTT[A/C]CTGAGCATTCTTAGC | 10533 |
| rs185861213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410993 | ATCTAATAATTCTCT[G/T]TTAATTTTTTTAAGT | 10533 |
| rs185876289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300119 | TTTGGTAGAGACAGT[A/G]TTTCACCATATTTGC | 10533 |
| rs185897923 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11336797 | CCCAGCTTAGCTTCC[C/T]GAGTATCTGGGACTA | 10533 |
| rs185911725 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11373487 | GAACCACCTGGAGCT[C/T]TTGTTAAACCTGCAG | 10533 |
| rs185952308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11441954 | TACAGGCGTGAGCCA[C/T]CGCGCCTGGCCCAAT | 10533 |
| rs185964930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11403993 | CTCCTTGTTGACATA[C/T]CAATATTTAAAAGAA | 10533 |
| rs185969398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531772 | GGGAGGCTGAGGTGG[A/G]AGGATCACCTGAGCC | 10533 |
| rs185979364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11288665 | TTTCTTGGGAGGCAA[C/T]CGCCACTGCACATTT | 10533 |
| rs185982061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283539 | TCTCAGCCAATAGGA[A/G]GTGGAGGTGGAATCC | 10533 |
| rs185987636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516124 | GCTATGTTAGTTTCT[A/G]GGGACTCTGAGATGG | 10533 |
| rs185991703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11482979 | CCCCTAATGATAACT[A/G]CAATTCTGACCTCTA | 10533 |
| rs185994778 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11457257 | TTTCCCAAACTCTTG[C/T]GGCGGGAAGATCTGT | 10533 |
| rs185997100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501962 | CCAAAGTGCTGGGAT[G/T]ACAGGCGTGATCCTG | 10533 |
| rs186001247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464012 | TGAGAGCATATCAGG[A/G]AGAGGAATGATTAAA | 10533 |
| rs186003207 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11294220 | CTCAAATCCTCAAAT[C/T]ACCTGTTTTCTTTTT | 10533 |
| rs186009549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11419511 | GTGAGCCAAGATCAC[A/G]TCACTGTACTCCAGC | 10533 |
| rs186033090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550900 | ATAATGAGCTTACCC[A/G]TGTTTGTATCTAGTA | 10533 |
| rs186050543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549746 | TTTCGTTTCTTTGGA[G/T]TAAACAGGAGTGGAA | 10533 |
| rs186062265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520414 | TGAGGGATATTTTGA[A/G]GATTAAAGAGCTATA | 10533 |
| rs186079380 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11550567 | TGCCTGGCTCATTTT[A/T]AAAAAATTATTGTAG | 10533 |
| rs186110004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272809 | TCTCTGGCACGTTCC[C/T]TCCCCATCTAAGCTG | 10533 |
| rs186128376 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287439 | TTCTAGGCCATGGGG[G/T]CCTGAGAGCGGCTGC | 10533 |
| rs186134846 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11310062 | TTCCAGCTACTGGGG[A/C]GCTGAGGTGGGAGGA | 10533 |
| rs186152406 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11553098 | AGGACACGGCCCACA[A/G]TGCTCACCCTTTTCA | 10533 |
| rs186183504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546531 | CACACAGAAATATAA[G/T]TGTGCCATTCCCAAG | 10533 |
| rs186194398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11512113 | GGCAGGGGAGGTGCC[A/G]AGAGCAAGCGAGGGC | 10533 |
| rs186256822 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11444142 | TACCCATTTGCTGTG[C/T]GGCTAAAGTTCATTT | 10533 |
| rs186278579 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538445 | CCATTTGCTAGCTGT[G/T]TGGCCCTGACAGTCA | 10533 |
| rs186310322 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11528098 | CATGTTGGGGACCAA[A/C]ATGAGAAGTAAACGA | 10533 |
| rs186312363 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452591 | CACTTCAGCAAACAG[C/T]GTGGTAGGGAAAAGA | 10533 |
| rs186315366 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11301756 | TGTCTGAAGATGGTA[C/T]GGGGGAGCATCAACA | 10533 |
| rs186318833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11477877 | CTTATTTCTCCCTGT[A/G]GCAGGAAACAGGCCT | 10533 |
| rs186327104 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11546802 | CAGCCCATCCCTGCC[C/T]TCTTCCATTGCAGGG | 10533 |
| rs186334547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512715 | CCCAAAGAGTGAGCA[A/G]TAGCAAGATTTATTG | 10533 |
| rs186351411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478388 | ATTGAGAACCAAACA[C/T]CCATTAATGGTGTGG | 10533 |
| rs186351624 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11497158 | GCCCAGCCCCTAATG[C/T]CATTTCTGATGAAAC | 10533 |
| rs186352955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527895 | TTTCATTTCCTTGTT[G/T]GTGACTACAAACACA | 10533 |
| rs186359172 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11389323 | ACTTGTTCATATAAC[A/G]TGTTATACTGTATTT | 10533 |
| rs186359517 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | ATG7 | GRCh38.p7 | 3:11418058 | CCTCGTTATCCACCC[A/G/T]CCTCGGCCTCCCAAA | 10533 |
| rs186366725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11436922 | ATGGGGGATTAAGGG[A/G]AAATCAGTGGCTACT | 10533 |
| rs186368593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459635 | TAGCTCTTCTTGTCT[A/G]ATAACAGCCAGAGTA | 10533 |
| rs186378650 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11398856 | TTTGAGCCCTTGCTA[A/G]GAAAAGCCTTAAAAC | 10533 |
| rs186400321 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11284235 | ATTTTAAAAAATCCT[A/G]TACTGGCTTGATTAT | 10533 |
| rs186410972 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491522 | GCTGGTGAGGAGCTG[C/T]GTTCCTTTGGAGGAG | 10533 |
| rs186412421 | snp | A/G | 4.9423e-05 | 0.00497082 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306990 | CTATTGGAACACTGT[A/G]TAACACCAACACACT | 10533 |
| rs186421801 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11473094 | CTGACTGCCACTTGT[A/C]CCTCTGACCTAGCCA | 10533 |
| rs186424567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330122 | CCTTATCACCTGATA[G/T]CCACATGACATCCTT | 10533 |
| rs186424847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350176 | CATTGTTAATGTTTT[C/T]GTCCATTTCACTAGA | 10533 |
| rs186426200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455697 | CCCTCAGAGTTAGCC[C/T]GAGCTGGCCACAACT | 10533 |
| rs186431089 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11408951 | TGTATATCTTCTTTG[A/G]TGAGGTATCTGTTAA | 10533 |
| rs186432443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369799 | GGTTGAAGGATGTCA[C/T]TTTGCCCCATGAGTT | 10533 |
| rs186434735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11435882 | AAAGTGGGCCACAGT[A/G]TAAGAGAGAACAGCA | 10533 |
| rs186465526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11413001 | ATTGTTCATTATTAG[C/T]GCATAGAAACGTAAC | 10533 |
| rs186466886 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473803 | TTTTTAAATGTAACC[C/T]TAGTGCCAGTTTCAT | 10533 |
| rs186479648 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11392479 | AAACAAACAAAAAAA[A/C]CAAAACAAAACAAAA | 10533 |
| rs186480946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11328549 | ATAAGAAAATTTTAT[A/G]TAACGGAAAAGGTAG | 10533 |
| rs186481386 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469757 | TTGGGAGGCTGAGGC[A/G]GGGTAGATCATTTGA | 10533 |
| rs186498451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432274 | CTAGACAAAGGAGAT[G/T]TACCCTATTCCATTT | 10533 |
| rs186502027 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11358912 | TGGTCTTATTCACCA[C/T]TACTTGGTCAATGAC | 10533 |
| rs186502499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11322001 | AGGGTTGCCAGTTCA[A/G]CAGCCCCCGGGACAT | 10533 |
| rs186519368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288164 | CTTTGTGCAGTATTA[C/T]GTGGCAAATAATCAT | 10533 |
| rs186531151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282323 | AAAAGAAAAACAGCT[C/T]CTGGAAGTAACCAAT | 10533 |
| rs186533158 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11310643 | TCTGTAGTTTTTTTT[A/T]TTTTTTTGAGACGGA | 10533 |
| rs186533615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336031 | ATGAGCCACTGTGCC[C/T]GGTCATTTTTTTTTT | 10533 |
| rs186537651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349409 | TGTGGTGGTGGTGTG[C/T]ATCTGTAGTCCCAGC | 10533 |
| rs186538753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11354713 | CTTGAGGTTTTAAAA[C/T]CCAAATCTGGACATC | 10533 |
| rs186550779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372896 | CCCCTTGTGGGGAGA[A/G]GGGAGAATGAGAAAA | 10533 |
| rs186559795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389081 | GGCGAAACCCTGTCT[C/G]TACTAAAAATACAAA | 10533 |
| rs186565444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11456722 | AATTACTGTTTGGAC[A/T]CAAAAATGTGACGGA | 10533 |
| rs186578940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11418543 | ATGGGGGCCTCCCTA[C/T]AACTAGGTCCCCCTG | 10533 |
| rs186580955 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11543794 | GTTATCCCGGCTACT[C/T]AGGAGGCTGAGGCAC | 10533 |
| rs186601751 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11525079 | ACTGGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 10533 |
| rs186609684 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280238 | TTTTTAGTAGAGACG[A/G]GATTTCGCCATGTTG | 10533 |
| rs186613534 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11517264 | GAGAATCGCTTGAAC[C/G]CAGGAGATGGAGGTT | 10533 |
| rs186615723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379834 | GAAAATACTCATTTC[A/G]AACTTATTTTTGCTC | 10533 |
| rs186622493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303266 | CTTGCAAAGAAGACT[A/G]GGAAGCGTGGAACCC | 10533 |
| rs186622618 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325081 | TGGTCACATGCTCTC[A/C]AGGTTTCTAGCCTAG | 10533 |
| rs186632693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11344729 | TAAAAATTAGCCAGG[C/T]TGTAGTGGCGCGTGC | 10533 |
| rs186633052 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11306066 | GTCCACATCTGAATT[C/T]GTATTCAGAATCAAC | 10533 |
| rs186637445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11365985 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 10533 |
| rs186642040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11385280 | TAATCTGCCCACCTC[A/G]ACCTCCCAAAGTGCT | 10533 |
| rs186658615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491672 | ATGTCCTTTCTGTTT[G/T]TTAGTTTTCCTTCTA | 10533 |
| rs186662023 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11305722 | AGAAGGTTCTGGCCA[C/T]TGAAAGCTAGCTCTC | 10533 |
| rs186746319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11434199 | CTGTGGAATATTTTT[A/G]TTTTGTTTTGTTTTG | 10533 |
| rs186757853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416355 | CTTTCTATTTGGGAA[A/G]GTTATTAATTATTGA | 10533 |
| rs186782250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11369122 | CTTTCTGCACAGGCT[A/G]TGTCCCCCAAATCCT | 10533 |
| rs186789743 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539444 | AGAGAAGGCATGGCA[C/G]TGAGCCGGGGAGGCC | 10533 |
| rs186801657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508419 | CAAAGCCATCCTGGG[C/T]CACATGCGTTAGACA | 10533 |
| rs186822520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11470762 | TTCCCTGAAGGGCCT[C/T]GGGAACTGAGCCGAG | 10533 |
| rs186831349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447416 | AGGTTGCAGTGAGCC[A/G]AGATCACACCATTGC | 10533 |
| rs186863819 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329568 | ACATTCACCGAGTGT[C/G]TGCTCTGTATTTATG | 10533 |
| rs186873514 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11492210 | GCAGTATTAGGGTGG[A/G]AGTGACCCGATTTTC | 10533 |
| rs186875727 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556510 | CGACGCTCAGTAGCC[G/T]GTAGCAATAACAAAC | 10533 |
| rs186893603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522452 | GGAATTCCGGAATAA[A/G]CTCACGATTTATTAG | 10533 |
| rs186901950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539864 | CCTGCCCTGCACAGC[C/T]GCCTGGAGGTTCACC | 10533 |
| rs186974782 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11289683 | CTACCTCAGCTTCCC[A/G]AGTTGTTGGGACTAC | 10533 |
| rs186977324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524051 | TCATTTCAAGTATGT[A/T]GCCCCAGGCCAAAAC | 10533 |
| rs186988942 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11311479 | TGTGCATGGCAGCCT[A/G]TAGTCCCAACTACTC | 10533 |
| rs187004557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516889 | GGAATTCAACAACAC[C/T]CTGGCCAACATGATG | 10533 |
| rs187006420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11278906 | GGGAAGGCTTCCCTC[A/G]GAAGTGATGATTGAG | 10533 |
| rs187008737 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11480152 | TAGCCAGCATGGTCT[C/T]GATCTCCTGACCTCG | 10533 |
| rs187009012 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11462438 | AGGCAGAAGACAGGA[A/G]CAAGGGGAAAGCATT | 10533 |
| rs187012138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337630 | CTAATTTTCTTAGAA[A/G]TGGCTATAGCCTTTA | 10533 |
| rs187027634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445124 | GTAAATTAGTTAAAT[C/T]GTTGTAGAAAGCAGT | 10533 |
| rs187077780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510747 | GTTTTTGGCCATACT[C/G]TTCTTGGCAGTCAGA | 10533 |
| rs187089405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11366549 | CATTTGAATCTTTCC[C/T]AAGTCTCCCGCCTTC | 10533 |
| rs187096959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385995 | CAATAACATGTAAAA[C/G]TCTTGCTCACCTAGC | 10533 |
| rs187098686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473886 | CCCCAAAACATCAGC[A/G]AGCCCTCAATTTCTG | 10533 |
| rs187117158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424939 | TGTGTCAGTACTATA[A/G]ACCTGCCTCATTCTT | 10533 |
| rs187125088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406240 | AGTGATCTGCCCACC[C/G]CAGCCTCTCAAAGTG | 10533 |
| rs187148771 | snp | G/T | 0.0165134 | 0.0893533 | intron-variant | ATG7 | GRCh38.p7 | 3:11340637 | CTTTGTGTTTTATTT[G/T]CCTTAAGATTGTCCT | 10533 |
| rs187151971 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11484552 | TTTTCTTTTTCTTTT[A/C]TTTTATTATTATTAT | 10533 |
| rs187152613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11541192 | GGCGTGAGCCATCGC[A/G]CCCGGCTGGTTTTAG | 10533 |
| rs187161445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447819 | TGATTGGCCAGCCTG[A/G]GCCAGGGGCAGGTCA | 10533 |
| rs187163539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379208 | CTGGTTTATTATAAA[C/T]GTTGAGTCCTATGGA | 10533 |
| rs187178505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428569 | TCAAGTTTCAGGAGA[C/T]GAATGGCATCTCTGC | 10533 |
| rs187184369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11409611 | TTTCATAGATCATGC[C/T]TTTGGTGTTGTATCT | 10533 |
| rs187188358 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468573 | ATTCATTAGCCCTCT[C/T]GATCCCCACAGAGAG | 10533 |
| rs187198086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405785 | AATGCATGTCACCAC[A/G]CCTGGATAATTTTTT | 10533 |
| rs187206611 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11316186 | GTGCAACACTACTGT[A/T]GAAGAATCTCCCTTG | 10533 |
| rs187219758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11532354 | AAACAGAGGAGGAAA[C/T]GGAGGAGGACAGAGC | 10533 |
| rs187220712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11502722 | CAGTAGAGAAAGCCA[A/G]TATTTCCCATAGAGC | 10533 |
| rs187221290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11341262 | AGACAGGGTTTCACT[C/G]TGTTGCCCAGGCTGG | 10533 |
| rs187222844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285519 | CATAAAGTGCACTGA[C/T]AGCAAATGTTTAGCT | 10533 |
| rs187226146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307776 | TAACCGCTGTAATCA[A/C]GGAGTCTTTATACCA | 10533 |
| rs187227496 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11359610 | GTGAGGCAGGAAGAT[C/T]ACTTGAGCCTGGGAG | 10533 |
| rs187227768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298232 | CTTGACAACACAGGC[C/T]AATTAGGATGGTTTT | 10533 |
| rs187232185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275916 | CAGCCTCTCTTTGAG[C/T]GTGTGGTACAGAAAG | 10533 |
| rs187238002 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485070 | ACCCAGTAATGGGAT[C/G]GCTGGGTCAAATGGT | 10533 |
| rs187239978 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11319256 | CTCTCTTTAGCATGA[G/T]TCCAGTTTCCCTTCG | 10533 |
| rs187244394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342055 | TTATTTCTTATTTTC[A/T]TGCATAGCCACTTGA | 10533 |
| rs187246926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389604 | GCTACTGCAAGTGTG[C/T]CAAATGTGAACAGTC | 10533 |
| rs187249732 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11465243 | GTGTGGATCCAGATC[A/C/G]AGACCATCCTGGCTA | 10533 |
| rs187251596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11365754 | CAGAAGAGGGGAAAC[A/G]ACTTCTTCATGGTCA | 10533 |
| rs187252777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448403 | TCAGGAGCTGGAGCC[C/G]CTGAGGTCAGCATGA | 10533 |
| rs187253417 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11361064 | TCCCTGATAGCACTC[C/T]GTATTGTCTCCGGTG | 10533 |
| rs187259103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381416 | TGGCTTTATGTTGGT[C/G]TGGCTAGTCAATGAA | 10533 |
| rs187281270 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397755 | CACCCACGCCCAGCC[C/T]GGAAATAAATGATTT | 10533 |
| rs187303096 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537649 | TCAGTCAATCCCAAG[A/G]GGGCTCTCACTCCAC | 10533 |
| rs187312123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505829 | CTCGCCATTGGTCTT[C/T]TGCAGTCTTGTCACT | 10533 |
| rs187341372 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11314829 | CTGTGGTCCCAGCTA[C/T]TCAGGAGGCTGAGGT | 10533 |
| rs187356280 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11324031 | GCAAATTGCTTGGCA[A/G]ACTGATCATGACTGA | 10533 |
| rs187358528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464898 | CCTTGTTTGGGTACT[A/G]TTAGGATTAAGTAAT | 10533 |
| rs187361504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358699 | TTCCCTTCCCCAGGG[C/T]AGAGATGTGGTTTGT | 10533 |
| rs187369206 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11428030 | GTTTCCACAAACTAT[A/G]TAAGGAAAACCTTGA | 10533 |
| rs187392153 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11488579 | CGCGGCCACCATGGC[C/T]GGACGGGCTCCCTAA | 10533 |
| rs187434705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548775 | GTCAGCTGGTTCCCC[A/G]CTGAGGGCCTCTTGG | 10533 |
| rs187450355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530391 | ATTTAAACAGCCAGA[A/G]TGACCTGAGCTTGGG | 10533 |
| rs187457186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11552868 | ACCTATGCCTCTTCC[C/T]CATAGCTAAAAACCC | 10533 |
| rs187457310 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344607 | CACGGTGGCTCACAC[C/T]TGCAATCCCAGCAGT | 10533 |
| rs187465548 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11515391 | TCACTGCAACCTCCA[A/C]CTCCCCGGTTCAAGC | 10533 |
| rs187466338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11312881 | AAGCAGAGTTCTGAT[C/T]TCTTCTCTGCCCCTT | 10533 |
| rs187468779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480277 | GGGTGGCTTATGCCT[G/T]TAATGCCAGCACTTT | 10533 |
| rs187471777 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ATG7 | GRCh38.p7 | 3:11500780 | GGACTACAGGCGTGC[A/G]CCACCACACCCAGCT | 10533 |
| rs187473103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11384548 | GGTTAGGTAGGAATA[A/G]TAAATGTCAGCTGGT | 10533 |
| rs187501243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11519622 | TGGAGTGCAGTGGGG[C/T]GATCTTGGCTCACTG | 10533 |
| rs187545834 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542129 | CGTCAGCGACAGGAG[C/T]CACTGCTCTTGAAAC | 10533 |
| rs187548723 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ATG7 | GRCh38.p7 | 3:11511141 | TTTATTGCAAAGAGC[A/G]AAAGAACAAAGCTTC | 10533 |
| rs187555735 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11511363 | TAGATACAGAGTTTC[A/C/G]ACACACAGGTTCTCC | 10533 |
| rs187556345 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524356 | TTGGGGTTTCCCTTC[A/G]ACTGTGAAATATTAC | 10533 |
| rs187567129 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11492353 | CATACACTGTCCTGC[A/G]CCCACTGTCTGGCAC | 10533 |
| rs187570426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474446 | CTCTACAAAAAATAC[A/G]AAAATTAGCTGGGCA | 10533 |
| rs187571704 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11429924 | GAATTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 10533 |
| rs187571915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11457945 | AGTAACCGGTAAGTA[C/T]ATATTGGTTGAATGA | 10533 |
| rs187583816 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411035 | TATTTTTTATGGTGG[C/T]TGCAGCATGTTACAT | 10533 |
| rs187623536 | snp | A/G | 0.000102965 | 0.00717441 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554875 | GGCTGACTTCTCCCC[A/G]GCCGCCTGCTGAGGA | 10533 |
| rs187643593 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | ATG7 | GRCh38.p7 | 3:11551700 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCACGAGC | 10533 |
| rs187661784 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11535493 | GTCTCAGAGCAGGCT[C/T]TCTTTGATGGATTAG | 10533 |
| rs187666444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475924 | CCCCTCCCAGAGTCC[A/G]AGCATTCTAGAGTTT | 10533 |
| rs187669427 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503558 | AGTCAGGAGGTCAAG[A/G]CCAGCCTGACCAACA | 10533 |
| rs187672846 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517789 | GCAGAGCTGGAGAGA[G/T]TCGGGCAATTGAGTT | 10533 |
| rs187674404 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485421 | AATTTGTTTGAGTTC[A/G/T]TTGTAGATTCTGGAC | 10533 |
| rs187686373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352925 | AGGAGCATTCCAGGG[A/C]AGAAAATTGGCCTTT | 10533 |
| rs187695020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461123 | AAGGCAAAGGGTGGG[G/T]CAGGGTTTGTGGAAG | 10533 |
| rs187699881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11371834 | AAAGACCCTTGGCAC[C/T]TTGTTCCCAGTGCAC | 10533 |
| rs187706343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391064 | TGTCAGTGTTTTCCG[C/T]TGATCTTTTGTCTGA | 10533 |
| rs187708815 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11424130 | CTTTTCACTGCTGCA[G/T]CTTTGCTCAACCTTC | 10533 |
| rs187715395 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11291458 | GAAGCTAGCAGACCC[A/G]GGTTATCATCTCAGC | 10533 |
| rs187724525 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11339050 | GCCTGTAATCCCACC[A/G]CTTTGGGAGGCCAAG | 10533 |
| rs187726038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437906 | AAGAATAATTCCATA[A/T]TACCACCTAAAATCC | 10533 |
| rs187730089 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11357123 | TTCCAGTAGGTGAGG[A/G]GTTTTGGCAAATGAG | 10533 |
| rs187755984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395681 | TGCAGTGGCTCACGC[A/C]TGTAATCCCAGCACT | 10533 |
| rs187767501 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11529473 | ATGAAGGGCCTTCTT[C/G]AAAATCAGGACTTAG | 10533 |
| rs187776131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498453 | CAGGTGCTATAATTT[C/G]CTTCACTTGCTATAT | 10533 |
| rs187790485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514511 | CAGGAAATACCGCCC[A/G]GTCTTTTTACCCACC | 10533 |
| rs187814744 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11311994 | AGACAGAAAATAGAT[G/T]AGTGGTTGCCAGGGG | 10533 |
| rs187820642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11338689 | TTTTAATTTTTCATG[A/G]CATTAAAAAATACCA | 10533 |
| rs187832304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11356503 | CTTGGGTGTGGACAT[A/G]ACTGATGGGCTCTAA | 10533 |
| rs187840456 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11375804 | ACCTTGTGATCCGGC[C/T]GCCTCAGCTTCCCAA | 10533 |
| rs187844666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11433612 | TCCTAAGTCCCTTTA[C/T]CCAATTTCCCTGAAA | 10533 |
| rs187848747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11394765 | CATTAAGATAATTCT[A/G]TTTAGCTAATGCCCA | 10533 |
| rs187852748 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11415608 | AAGACACAACATACA[C/T]ATTAGCCTACGCCTA | 10533 |
| rs187878633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548669 | TCTTTCACTAAAGAA[A/G]TCCCGGAACTGAGCC | 10533 |
| rs187887627 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ATG7 | GRCh38.p7 | 3:11374691 | CGGGCAGATCGTGAG[A/G]TCAGGAGATTGAGAC | 10533 |
| rs187891570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345790 | TTTTCCTCCTTCTGT[A/G]GAATTTATTTTACTG | 10533 |
| rs187943443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462602 | CTGGGATGATGAAAG[C/T]AGAGGAATTTTGCCT | 10533 |
| rs187958597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11415031 | TGTCCTTATACAAAC[C/T]GTGACAGCATAAGCC | 10533 |
| rs187967395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478522 | GGGGTTCCAGAGAGC[A/G]CGTTTTTAGCCACTA | 10533 |
| rs187968871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304113 | AAAAAATGTTTTTCT[C/T]TTCTATGCCTCAAGT | 10533 |
| rs187988279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444787 | TAGATAATCTACAGA[A/G]TGGGAGAAAATTTTC | 10533 |
| rs187992495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11282095 | GAGGTAACAAAAGGA[C/T]TCAGAAGGAGGCACA | 10533 |
| rs188007812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405987 | TTCCTTGCTTTTTTT[G/T]GTTTTTGTTTTTGTT | 10533 |
| rs188024807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11279801 | AATTTAGATATCCCT[C/T]CTCCTATAACATTCT | 10533 |
| rs188030346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11376501 | GTGGTTTTTAAGGAA[A/G]GTGAACACTTAGATA | 10533 |
| rs188030817 | snp | C/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11330489 | TGCCTGTATCACCTT[C/G]GCATGCCCCAATTCA | 10533 |
| rs188055651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370454 | CATTTTGGCATTGAA[C/G]TTGATTAAGACTCTT | 10533 |
| rs188059769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513997 | GCCTCCCAAGTAGCT[A/G]GAAGAACTACAGCTA | 10533 |
| rs188060391 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11439326 | TGCCCGTCTCAGCCT[C/T]AGAAAGTGCTGGGAT | 10533 |
| rs188073586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11402399 | GATTGTGCCATTGCA[C/T]TCCAGCCTGGGCAAT | 10533 |
| rs188074304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11529904 | TTTGCCCTTTTCTTA[C/G]TCACCCTAGCATGAC | 10533 |
| rs188074823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518280 | GGCTGGGCACAGTGG[A/C]TCACGCCTGTAATCC | 10533 |
| rs188089436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505113 | GGAAGCTGGGAGCCT[C/G]TTAATTTTCATAACA | 10533 |
| rs188093463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466992 | AATTAGGTGTGGTGG[C/T]GGGCGCCTGTAATCT | 10533 |
| rs188122979 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285220 | ATTCTCACCCTGTCA[C/T]GCAGGCTGGAGTTCA | 10533 |
| rs188165906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325747 | AATTGCTAAAGGTTA[C/T]ACAAGAGCAAGTGAT | 10533 |
| rs188178511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394341 | TAAACCAGCTCTCTT[A/T]CTGAAGTCACCTTAA | 10533 |
| rs188223407 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11352333 | GCATGTGTCTTTATA[A/G]CAGCATGATTTATAA | 10533 |
| rs188245166 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11281175 | GTGATTACTTAGGGC[G/T]GCCTCATACAGTTAT | 10533 |
| rs188253047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11407338 | TCTTGGGCAGCTCTG[C/T]CCCTGTGGCTTTGCA | 10533 |
| rs188258070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11356306 | TTATGTAAATTATAC[C/T]TCAACTTGGCTACAC | 10533 |
| rs188264828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546296 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10533 |
| rs188265912 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11274881 | TCTAAAATGTGGGGG[C/T]GGGGGTGGAGAGCAG | 10533 |
| rs188301804 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11539236 | TCACAACAGCCCTAC[A/C/G]AGGGAGACAGCATTT | 10533 |
| rs188310797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509683 | CTAATTTTAAGATGT[A/G]ATTCACTAGGAAAAT | 10533 |
| rs188312212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11305444 | CTGTGCTTGTGTCCA[A/G]ATTAGATCATGGCAT | 10533 |
| rs188318496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11327798 | GAGGAGCAGTGCTTC[C/T]GAAACTTCCATGGGT | 10533 |
| rs188319047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11523272 | AGCGGGGGAGTGCAG[A/G]GGAGGGGAAATAGGG | 10533 |
| rs188319615 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11492886 | GTCCAGGTGGGGGTG[C/T]CTGAAACTCCAAGGC | 10533 |
| rs188325955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347565 | TTTTAAAACAACAAC[A/G]TAGACAATTCTTATG | 10533 |
| rs188326679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458263 | AAGTCAGACTTGGGT[A/T]TTTTTGTTTTGTTTT | 10533 |
| rs188328393 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11368544 | CCCCTGTAATCCCAG[C/G]ACTTTGGGAGGCTGA | 10533 |
| rs188328857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351145 | CTATTACTTACTTGC[A/G]TGTCAGGTAGTGTAT | 10533 |
| rs188333274 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11491544 | TTGGAGGAGGAGAGG[C/T]GCTCTGCTTTTTAGA | 10533 |
| rs188340387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387752 | GAGGCAGGCGGATCA[C/G]GAGGTCAGGAGATTG | 10533 |
| rs188348909 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11421259 | TTCCTTTCAGAAGAT[A/C]TTCCTCTGTAGCATG | 10533 |
| rs188352056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447109 | TGAAAAACCTTTTGT[A/T]GCCATCCATACCCTG | 10533 |
| rs188365149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11426345 | TTTGTGAAGTACCTA[C/T]TGAAATTTATTTTTC | 10533 |
| rs188373173 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11407844 | GACCCTGGGCTCAGC[C/T]CTTGAAACCATTTTT | 10533 |
| rs188410784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307217 | TCCAGAGAGAATACT[A/C]CCAGCTGTCTCCTTC | 10533 |
| rs188413409 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515984 | GAAGGGCAGGGTAGA[A/G]GCATGGGGGAAGGAC | 10533 |
| rs188418733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388908 | ATATGGTCTTACACA[C/T]ACAGGCTTTATACAA | 10533 |
| rs188430248 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11481303 | GTGCAGTTAAAAATG[A/G]TTATAATTGTAGGTT | 10533 |
| rs188434711 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501783 | CAGCCTTCGCCTCCC[A/G]GGTTCAAGTGATTCT | 10533 |
| rs188435274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11473289 | TATTTTCTGACTGCT[A/G]TCACCTACCCAGGAA | 10533 |
| rs188436853 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11456019 | CAACTCACTCTTCAA[A/G]AATATACAGTTCAAT | 10533 |
| rs188446243 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11463844 | TGGGCCCAGCTGGCT[C/G]TCTTGCTCATTTTGG | 10533 |
| rs188451373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436110 | TATAGGGAACTCTTA[A/C]AACTTAATAATATAA | 10533 |
| rs188471488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11296299 | CTTGCTTTGCCTCTC[A/G]AGGGTCTTCTCTTTC | 10533 |
| rs188478868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465688 | AAGGATTGCTTGAAC[C/G]CAGGAGGTCGTGGCT | 10533 |
| rs188493469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331866 | ATTAAGGAAATAAAA[A/G]TTAAAACCATAATGA | 10533 |
| rs188496020 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11429155 | CAGGTATGTATTTTT[G/T]GGCCTGCCCAGTTTG | 10533 |
| rs188536253 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390126 | TGTGAGCTCAACATC[A/C/G]CTCTTTCTTAAAGAA | 10533 |
| rs188536344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525429 | CTTTACTCATAAGAG[G/T]TTCACAGTAAGACAT | 10533 |
| rs188555482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11321147 | TGCACACAGTTCTGC[A/G]TCTAATGTCAGAGAC | 10533 |
| rs188567373 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11344140 | AATAGTGAATTTTGC[A/G/T]TATTTGTCTTTGGCC | 10533 |
| rs188571316 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363766 | GAAAATCGAATTTTT[A/G]AAAGATTTATTTTTC | 10533 |
| rs188581864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383151 | GTTTATACCAGTTAA[C/T]GTTCATTATAGGTTT | 10533 |
| rs188582792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292248 | TATTTTTTTCTTTCT[C/T]TCTTTCTTTTTTTTT | 10533 |
| rs188592631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313517 | GGCACTTCTCTGGAT[A/G]AAGACGTGGTAACTG | 10533 |
| rs188599312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11404610 | AGCCTTGTGCCTGTG[C/T]CATGTTGTATTAGTC | 10533 |
| rs188599499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450491 | CTGGGACTAACTCCC[A/G]CAAAGCAAGGTCACA | 10533 |
| rs188600999 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11554151 | TTCTCCTCACAGCCA[C/T]GTTGGGGCCTCCTGC | 10533 |
| rs188605470 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430503 | CTAAATTAATTCTCA[C/T]TTTGGGTTAACTATT | 10533 |
| rs188608751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339781 | GATATGGAGAGCCAC[A/G]TAAGTGTGGGAAACA | 10533 |
| rs188612429 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11450040 | CAAATCTTACAGGGT[A/G]GTCTGTTTCTTCTTT | 10533 |
| rs188613503 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11358019 | GTCTCAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 10533 |
| rs188613816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11411400 | GGAGCCCAAGGTGGG[C/T]GGATCATGAGGTCAA | 10533 |
| rs188659825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11552040 | AGGCGTGCGCCACCA[C/T]GCCCGGCCTCTTTCA | 10533 |
| rs188665725 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11517944 | GGCACAGTGTGAGGG[A/G]TGGATTGGGGTGATC | 10533 |
| rs188693661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380328 | TGTCTTGAATTTGAA[C/T]TTTACTGCTCTTTGT | 10533 |
| rs188701393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11544263 | CAGACCCTGGGCCTT[A/C]ACCCGGCAGCACTTC | 10533 |
| rs188738526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420988 | TCTCAATCTCCTGAC[A/C]TCGTGATCCGCCTGC | 10533 |
| rs188751438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297393 | TGTTCATATGTTCTG[C/T]TGCAGAAATACTTGT | 10533 |
| rs188768918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448868 | CAGAATCCAAGGCAG[G/T]CCCTGGGGGTCTCTC | 10533 |
| rs188770590 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11341357 | GAGCCACCACACCCA[C/G]CCCTTATTGGCCCAC | 10533 |
| rs188787075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410769 | TGAATAATATTTCAT[G/T]GTATGTAGCATATAC | 10533 |
| rs188809631 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11371239 | TTGTTTATTTGAAAG[C/G]GAAAAGGAAGAGAAG | 10533 |
| rs188811625 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ATG7 | GRCh38.p7 | 3:11511628 | GGCGGTCGATGGGAC[C/T]GGGCGCCGTGAGCAG | 10533 |
| rs188832217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290296 | TAAGTCCTAGGCTGC[C/T]TTCATTCAGCACCTG | 10533 |
| rs188836302 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11507604 | TTCCCTCCATTATAA[G/T]TGAAGGAAATGCTAA | 10533 |
| rs188842396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445643 | GTCATGGGTTTACCT[A/G]TATAATAAGCCTGCA | 10533 |
| rs188849195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470300 | CCTTAGGTGGCATAG[C/T]CTGCTACATACTTAG | 10533 |
| rs188858153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406795 | CATAAGACCCATTAA[C/G]CATCACCAGAGCAGC | 10533 |
| rs188868177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11504395 | ACCCTATGCAAACCA[C/T]TGGAGGATGAACTCC | 10533 |
| rs188876479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11466335 | TAAGGTGAGAAAATT[A/C]TTCAGCAAATTCTAG | 10533 |
| rs188904961 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11549889 | CATCCTCACAGACAT[C/T]GGGCATCGCTGGCCT | 10533 |
| rs188927595 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11502020 | TCCTAAAATGGTAGT[A/T]AACATATATACACAC | 10533 |
| rs188931506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516200 | ATAAACACATGAAAA[A/G]ATGTTCCAATAGCAT | 10533 |
| rs188933431 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349118 | TGCTGATTGGTGTGT[G/T]TTTACAGAGTGCTGA | 10533 |
| rs188955517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11552619 | CAGTGGAGAGCCCGT[C/T]CCTGCCCCAGAGATT | 10533 |
| rs188956007 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11535830 | CCTGCCAGCTTCGCA[C/T]CCTTGCTTGAATGGT | 10533 |
| rs188976591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11505595 | GTCCTTACCTCCGAC[C/T]GCAAAAGAGTCTTCT | 10533 |
| rs188984797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11518908 | AGCTGGTAAATGAAG[A/G]AAAAAGACCTGTTGA | 10533 |
| rs189014585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455544 | TACAATTCCTTCTTC[C/T]GGTGACATCCATTTT | 10533 |
| rs189020581 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11435574 | AAAGTGTATGAGTAA[C/T]CCGAATCCTGGCCTG | 10533 |
| rs189021450 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11275418 | CAGTGGCACGATCTC[A/G]GCTCACTGCAAGCTC | 10533 |
| rs189028483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401188 | CAGCTACTTCTGTTT[C/T]AACAAGCCTTCCTGG | 10533 |
| rs189045546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11317540 | AGACTCAAAGTCACA[C/T]GACCACATTGTCTGA | 10533 |
| rs189079492 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11512065 | CAGTGGGGGGCTGAA[A/G]GGCTCCTCAAATGCC | 10533 |
| rs189096809 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11477311 | ATGTAAATAAGAATT[A/T]TTGTGCTACAAACTC | 10533 |
| rs189106888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442204 | AGCTCTCTTCAGCCC[C/T]TAGCAGTGTGGGCCC | 10533 |
| rs189110440 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489517 | TTCTTGCCTTCTGCT[A/G]GCTTTTGAATGTGTT | 10533 |
| rs189129998 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11425164 | AGACAAGGTCTCACT[A/G]TGTTGCCCAGGTTGG | 10533 |
| rs189132224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453610 | TCTTCTATGTGGGGC[A/G]ACATCATTTAGCTCT | 10533 |
| rs189172951 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11421861 | CTTAGCATGCATGAA[A/G]ACAACATTTATCTCT | 10533 |
| rs189183647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402868 | CAATTACCTGGTTAC[A/G]TAGACTTACCAGATT | 10533 |
| rs189184783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11302407 | TCCTTTATTATTACC[C/G]CATTTTTGTTTTGAT | 10533 |
| rs189217172 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11530575 | TTGATGGTGAAATGA[A/G]TCCCCTCCTCTGAGA | 10533 |
| rs189219814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287596 | CTTAAGATGTAGAAT[A/G]CTGCTGATGCAGTCT | 10533 |
| rs189225919 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11342660 | TTTATTTTTAACTAG[A/G]TAGAAAAATGACTGT | 10533 |
| rs189235076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310234 | ATCTTTTCTCCTGCT[C/T]ATTTTACTTCTTTAG | 10533 |
| rs189235291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361531 | CTCGTGATCCACCTG[C/T]CTCAGTCTCCCAAAG | 10533 |
| rs189240616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308661 | CCTGATGTGCCTGGT[A/G]TATAGTAGACAATAA | 10533 |
| rs189244912 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11334039 | CAGGCATGAGCCACC[A/G]CTCCCGGCCAGCTTC | 10533 |
| rs189247430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382358 | GGTGGGGAAGAATAC[A/G]GTGCTTTGCTTCTAA | 10533 |
| rs189248772 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11278065 | GGCAGTCAGACCTTA[C/T]GGTTGTCTTCCCTTG | 10533 |
| rs189251500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354333 | TCTTTTATAAATCAT[A/G]TAGCTATTTGAGGCA | 10533 |
| rs189262067 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11458412 | GGGACTACAGGCGCC[C/T]ACCACCACGCCCGGC | 10533 |
| rs189270260 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11440258 | ATGAACTTGCGACTC[C/T]AATCCCAACTTACCA | 10533 |
| rs189282509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458582 | TTTGGGTTTTACTTA[C/T]AGCCAGCTCAGCTAT | 10533 |
| rs189315385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286112 | AACACCACAGATGCT[A/G]TGTTCTTTCCATGGC | 10533 |
| rs189324405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11501393 | ATACTAGCTGTTATT[A/G]TTTGTCAGAAGGACT | 10533 |
| rs189331371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526385 | TGGCAGAGTGAGACT[C/T]AAGTCTCAAAAACAA | 10533 |
| rs189354362 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11463063 | GCTAATTTTGAATTT[G/T]TAGTAGAGATGGGGT | 10533 |
| rs189360497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398717 | AATTGCCAGGTGTTA[C/T]GGCACATGCCTGTAG | 10533 |
| rs189360811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496126 | CCATTCCGTGAGAGG[A/G]AAGGCCATTAAAAGG | 10533 |
| rs189362061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476207 | TTTGGTTCTGGCTTT[C/T]TCTTTTCCTTCTTCC | 10533 |
| rs189363710 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11425737 | AATGAATTCTCAAGA[A/C]GTACACCTTATGTAA | 10533 |
| rs189366599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495258 | TATGGACAGAATTAA[A/G]GATCATGGGATGAAT | 10533 |
| rs189369021 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11552372 | GATATTTTTTAAAAT[G/T]TGCCAGTTTACTATG | 10533 |
| rs189380030 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | ATG7 | GRCh38.p7 | 3:11490681 | GGTGGTGACAAAATC[G/T]CTCAGCATTTGCTTG | 10533 |
| rs189383303 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11458732 | AAAAAAGAGAACTTG[A/T]TTCAACAAGATAATT | 10533 |
| rs189390615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304781 | AGTATACGCATTATC[G/T]CAAGTTCACTATTGG | 10533 |
| rs189392704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281641 | TACCTGGGCGTAGTG[A/G]CGGGCGCCCATAATC | 10533 |
| rs189394194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454988 | AGATAGCATAACATA[A/T]GGAAAGATAGCCTGA | 10533 |
| rs189399933 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11423126 | GGACACTTTGAGGCC[A/G]TTGTAATTGGCCTAC | 10533 |
| rs189410043 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11416849 | GTGATACAGATTTCT[G/T]TCTCTAAGCATTTCT | 10533 |
| rs189426212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348433 | GTGGGTTCTTGGTCT[C/T]GCTGACTTCAAGAAT | 10533 |
| rs189430593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11548921 | TTAAGCCGTAGGAAT[A/C]GTGGCTGTTGCCAGA | 10533 |
| rs189451488 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527258 | TGCAGGCACATGCCA[A/C]CACACCCAGCTAATT | 10533 |
| rs189476367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340063 | GATTAAAAGAGGGCT[G/T]CGGGGAAGGGAGAAG | 10533 |
| rs189484697 | snp | C/G | 1.7536e-05 | 0.00296103 | intron-variant | ATG7 | GRCh38.p7 | 3:11358396 | TTGCTCCAGACATAA[C/G]TACGTCCTGGTGTTT | 10533 |
| rs189486951 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11548884 | GGACAGACTCCTAAA[A/T]GTGAGACGGCCGGGT | 10533 |
| rs189490517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11378863 | AAATTGTTTGTTTTT[C/T]GGGGGGTGGGGGATT | 10533 |
| rs189497338 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11515767 | TTAAGTAAGATGGAC[C/T]CTTTTCCTCAAAGAG | 10533 |
| rs189497949 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11305744 | CTAGCTCTCCCTGAG[G/T]ACTTGGCATTTGAGC | 10533 |
| rs189514735 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11377087 | GGTAAAAAATGACAG[A/C/G]CCTCAGAGCTGTGTA | 10533 |
| rs189524413 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11417848 | ACAGAGTCTTGCTCT[A/G]TCACCCAGGCTGGAG | 10533 |
| rs189530297 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11397276 | AACTTAAATACCACA[A/G]GAAAGCTGCTGTAGC | 10533 |
| rs189585744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11372063 | TCCCCACGGTGAGGA[C/T]GGTGTGTCCTGTCTC | 10533 |
| rs189630659 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11480624 | GTTTCCTCGACTTCA[C/T]CTAAAGGGTATCTGG | 10533 |
| rs189632929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418129 | ATATTTTTTAAGGTA[A/G]GGTCTCACTCTGTTG | 10533 |
| rs189638856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446275 | AAAGGTTACTATATC[A/C]ATTTCAACATTCTGT | 10533 |
| rs189661584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471346 | ATTCTTCATAGAGGC[C/T]ACTTGGGTTCTGCCC | 10533 |
| rs189665072 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286999 | CATGAACTCCTGCCC[C/T]CAAGCAGTCCTCCTG | 10533 |
| rs189679269 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11334943 | TGGGTGACAGAGCAA[G/T]ACTCTGTCTCAAAAA | 10533 |
| rs189682959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434953 | TTCAGTGTCCTGTGC[A/G]TGCTTCCCCACTTAA | 10533 |
| rs189695197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396513 | TACAATATTGAGTGG[A/G]ATATTTTTTAAAAAT | 10533 |
| rs189700391 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11531466 | CCAGTCCATTACTGG[A/C]TGGCATTAGGGTGCT | 10533 |
| rs189708754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368918 | TGAATGTGTATATGC[C/T]ATTCTTCTGAGCTTG | 10533 |
| rs189722892 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11492355 | TACACTGTCCTGCGC[A/C]CACTGTCTGGCACTC | 10533 |
| rs189735982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11509198 | AGCGCCACATGGCCA[A/G]CAGCTTTTAGCTTAT | 10533 |
| rs189749751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11469502 | AACCTACCTATTAGT[C/T]CACTGATTTTCTTTC | 10533 |
| rs189755881 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424135 | CACTGCTGCAGCTTT[A/G]CTCAACCTTCCCTCC | 10533 |
| rs189764145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11452322 | CCCAGGAGGTGGAGG[C/T]TGCAGTGAGCCATGA | 10533 |
| rs189766259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432043 | GCTGTTGAGATTAGC[A/T]GGCAAATTACCAAGT | 10533 |
| rs189779311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282438 | CAGAGTTGGCTTGGA[A/G]GTGAGGAGGACAACT | 10533 |
| rs189783705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328567 | ACGGAAAAGGTAGCA[A/G]ATATTTTAAAGAGTG | 10533 |
| rs189788329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11524871 | TGTCATCCTCCAGGT[A/G]AGGTTCTGTGTCTTA | 10533 |
| rs189797030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11542287 | TTGGTGCTTATTTAG[C/T]GACATCCCCAGAGGG | 10533 |
| rs189800953 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11511153 | AGCAAAAGAACAAAG[C/T]TTCCACAGCGTGGAA | 10533 |
| rs189816110 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11538556 | GACACAGAATAGGCC[C/G]TTAGTGCCAGCCTCA | 10533 |
| rs189816832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277543 | GTAGGACTGTGATGC[C/T]GACCCGAGCTGCAAA | 10533 |
| rs189826606 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11506132 | GCCTTCTTTCCCTAG[G/T]ACATTTATTATTACT | 10533 |
| rs189834671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521152 | GATCATGAGATAATA[C/T]ATGTGCAGCATTTCA | 10533 |
| rs189836819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488662 | TGACCTCCTCTCAAG[A/G]TGTGAATGATTCTTC | 10533 |
| rs189845736 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11353618 | CATGAATGGCTTGGT[A/G]CCCTCTCCACATTAA | 10533 |
| rs189866152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391378 | AAGGATGAATTCTCA[C/T]TTCCTGGAGGCTGAA | 10533 |
| rs189868407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273365 | CCTGTTTGGTCCTCC[C/G]CCAGTTCTGACTCTT | 10533 |
| rs189907890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509520 | TGTTTGCTGACAAAT[G/T]GTTTGTATTTTATGA | 10533 |
| rs189925631 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472794 | TTTGTGATTGGTCTG[A/G]TAGCTCCAGTGTTTG | 10533 |
| rs189926690 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309580 | TGCCCAGTGAAGAAG[A/G]GGTAGGATGTAGATG | 10533 |
| rs189949964 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11272797 | CTGGATTTGCTGTCT[C/T]TGGCACGTTCCTTCC | 10533 |
| rs189952467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330372 | TATCAGTGTGGACTC[A/G]TAGATACTTATTTTA | 10533 |
| rs189956582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350749 | TTGCAAAGAGTGAGG[A/T]TATATAATATTACTA | 10533 |
| rs189968501 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11370327 | TAGTTTTTCTGCCCC[A/C]TTGGTGACTCTAGCT | 10533 |
| rs189970850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315053 | TCATAGGAGAGAAAG[A/T]ATGTTTCGTTACCGC | 10533 |
| rs189973027 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11341061 | ATTGGCCCACTCCCC[C/G]GCCCCGTCCCCCACC | 10533 |
| rs189975901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11389503 | TAGAATATCTAATGA[C/T]TGGTTAAATCACATA | 10533 |
| rs189978865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11540780 | AGTTTTGAATTCTGA[A/G]GTTCAGTTAATAATT | 10533 |
| rs189987533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358952 | GGGCAACAATGTTGA[A/G]TAGTGAACTAAATCA | 10533 |
| rs189993392 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11379867 | AATCTCTTTCCGGGC[C/T]GCCATATTAATCATT | 10533 |
| rs190002686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428190 | AATGATTGCATGGGT[C/G]CAAAGATCTATAAAT | 10533 |
| rs190009072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409084 | TTGTAAATAGTTTCT[C/T]GTGGCCTGCAGCTGG | 10533 |
| rs190033512 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11307036 | TGCAGATAAGAAGCT[C/T]CTTTTGGAACAAGCA | 10533 |
| rs190050191 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11295975 | TAGAGACGGGGTTTC[A/C]CCATTTTGGTCAGGC | 10533 |
| rs190050456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11274487 | AGGTGAAGAGTGGTT[C/T]GAAGTGAGATGAGCA | 10533 |
| rs190088178 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392096 | TATTTCTTATGGTCA[C/T]GTTTCAGACTGTAGC | 10533 |
| rs190090742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298993 | TTCTATTTTACTTCC[G/T]GACTTTTTGATCCCA | 10533 |
| rs190107913 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | ATG7 | GRCh38.p7 | 3:11465626 | AAAAATTAGCTGGGC[A/G/T]TGGTGGCACACACCT | 10533 |
| rs190113593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301336 | CTTTATTGTACCTCA[A/G]CAGTATCAAGATGGG | 10533 |
| rs190114158 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448516 | CTAAAAACTTACTTG[C/T]CGTGCTGAAACTTGT | 10533 |
| rs190118437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428572 | AGTTTCAGGAGATGA[A/G]TGGCATCTCTGCTGC | 10533 |
| rs190130263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409679 | CTCCCATGTTATCCC[A/G]TAGGAGGTTTATAGT | 10533 |
| rs190144208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319772 | TTCCCCCTACCACCC[C/T]TGTGTCTTGTGGATT | 10533 |
| rs190150041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11523101 | TGTAGGAAATGCTTC[C/T]TTGGGTGTTTGTATT | 10533 |
| rs190156440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11468278 | ATCTGCAGTCTCTGC[A/G]TAAGTGAAGAATGAG | 10533 |
| rs190157688 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491041 | TAGATTGGGGAATTT[C/G]TCCTGAATAATATCC | 10533 |
| rs190171005 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11430995 | AGGCCAAGTCTTTAG[C/T]ATATTACTCAAAATC | 10533 |
| rs190200675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11278597 | TTAGAAAAACAATGA[C/T]GAATAGGGGAAAATG | 10533 |
| rs190213750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11422641 | CTAGAACTTTCCCTT[A/G]GCATTAACAACTTGG | 10533 |
| rs190216412 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557957 | AAACAGTAACAACAA[C/T]AAACACACAAATGGT | 10533 |
| rs190242234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519649 | ACTGCAAGCTCCCCC[G/T]CCCAGATTCACGCCA | 10533 |
| rs190244344 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382710 | TCAATATTCCTGAAA[G/T]AATTTCCTGTAGTGC | 10533 |
| rs190269224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488613 | ACCGACCCCAGCCCG[C/G]GGGCCTTCGAGCCTT | 10533 |
| rs190301767 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11300461 | AGCTACAGGGATTTT[C/G]CTATCTTCTACAGAA | 10533 |
| rs190328709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343686 | AAGGGGTAAAGATCT[A/G]GCTACTTTTGCACAA | 10533 |
| rs190361092 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11534085 | CTCCTCCTCCCCCCC[A/C]AGGGGAAAGCTGCCA | 10533 |
| rs190371439 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ATG7 | GRCh38.p7 | 3:11541146 | ACTTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 10533 |
| rs190377821 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11517514 | ATCTCTGGTCTAGTC[A/C/G]GAGTCAGCAGGCACA | 10533 |
| rs190385406 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485071 | CCCAGTAATGGGATG[C/G]CTGGGTCAAATGGTA | 10533 |
| rs190386744 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11366671 | TCCTTCTTTAAGTCC[G/T]TTATGTTAAATTACT | 10533 |
| rs190388039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11503215 | AAGGCCATAGTGGAC[C/T]TCAGACAGCTTCTGA | 10533 |
| rs190399585 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11486768 | GTTGAATTTTGTCAA[A/C]GGCCTTTTTTGCATC | 10533 |
| rs190401175 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11483779 | TGGGTTTTGTACACA[A/G]TGACCCTGCAGCCAA | 10533 |
| rs190403186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457535 | ATTGTTCTGTACCCA[A/G]GAGTTCAATAAACAC | 10533 |
| rs190407477 | snp | A/G | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451440 | GGTCCTGACCTCCTG[A/G]CCTCAAGTGATCCAC | 10533 |
| rs190410914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11437634 | AGTTGAATGAAAAGT[A/G]CAGTGAATACCCACA | 10533 |
| rs190423397 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11412489 | TTGTTTCTGCGCTCT[C/T]TATTCTGTTTCGTTG | 10533 |
| rs190425331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372744 | TCAGAGGGAGGCAAG[A/G]TTTGGTCACTCTGAG | 10533 |
| rs190426384 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11401007 | TTTAAAAATGTGCTG[C/G]TTAATGGGTTGAATC | 10533 |
| rs190448260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441331 | TTACTGAAACCTCTG[A/C]CTCCAGGTCTAAGAA | 10533 |
| rs190453601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359638 | GAGGTTGAGGCTGCA[A/G]TGAACCGAGATCACG | 10533 |
| rs190463904 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | ATG7 | GRCh38.p7 | 3:11380112 | GGTCAGCATTTGACC[C/G/T]CAGCCTCACCAGCTG | 10533 |
| rs190469879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403533 | TGGAAACTAGCAAAT[C/G]TAAACTTTTATGTAG | 10533 |
| rs190470524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326153 | TAAAACACATACCTG[C/T]TTACTGTTAAGCAAG | 10533 |
| rs190478747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492290 | ACCCCTTGCACTTCC[C/T]GAGTGAGGCAATGCC | 10533 |
| rs190481379 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293622 | GTACATCAAGGCAGG[C/T]GGATCACTTGAGGTC | 10533 |
| rs190489309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473907 | TCAATTTCTGTGCAT[A/G]CGTTCAAACCTCAGG | 10533 |
| rs190510922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505873 | ATTCAGAGAGCTGAA[A/G]GGTACACAGTGCAGT | 10533 |
| rs190512861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552927 | CCTCCCTGAAAGTTT[A/C]TACTTTCCTATAAAG | 10533 |
| rs190521233 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468766 | GGACTGTACGCAAAA[C/T]GTTACGTGTGTGTAT | 10533 |
| rs190537070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11497001 | GGATTACAGGCGTGC[A/T]CCACCATGCCCAGCT | 10533 |
| rs190540975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478042 | ACTAATTCCTGTTGC[A/C]GAGTAAATAGCACAG | 10533 |
| rs190542589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458919 | AGATTCTCATAGGGG[C/T]GGGAACACAATTGTG | 10533 |
| rs190561448 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11320734 | GGTGTGTAAAATGCA[A/G]TGGAAGGATGAATTC | 10533 |
| rs190584424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362162 | AAGGTAAAATTTTTA[C/T]AGAGTCAAAAATATC | 10533 |
| rs190597885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11311553 | GTTGCAGTGAGCTGA[A/G]ATCGTCGTGCCGTTG | 10533 |
| rs190611934 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11383633 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 10533 |
| rs190615733 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337709 | CTGGCCTTGAACTCC[G/T]GGGCTAAATCCTTCC | 10533 |
| rs190620058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356353 | GAGTTTTAGAAAATA[C/T]TGGTGCCTGGGCTCA | 10533 |
| rs190627070 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11548011 | CACACCCAACTAGTT[C/G/T]TTAAATTTTTTTGAT | 10533 |
| rs190628307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11375105 | CTGTAGTCCCAGCTA[C/T]TGGAGAGGCTGAGGA | 10533 |
| rs190645264 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11386901 | GTATTTAGCTACAAG[C/G]CTTAACCTCAGAACT | 10533 |
| rs190657261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11443186 | GTGTGGGGCGTGCTC[C/T]CACCTCCAGCCTGCT | 10533 |
| rs190663608 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11423370 | AAAGTTTGAAATATT[G/T]TGAGAATTACCAAAA | 10533 |
| rs190671453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11405384 | TGAGGCGATGAGAAT[A/G]GGAGAAGTTGAAATG | 10533 |
| rs190712194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11414113 | CTTGCTCTTGTTGCC[C/T]AGGCTGGAGTGCCAT | 10533 |
| rs190720396 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271878 | AACACCTGTCCAGTG[C/G]TTTGCACGCGCAGAG | 10533 |
| rs190722314 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11521577 | TTTTTTTTTAAGACG[A/G]AGTCTCGCTCTGTCA | 10533 |
| rs190724841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11346649 | TCCCACTACCCAGCA[C/T]GTTCCCAGAGTGCCT | 10533 |
| rs190728638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553741 | GGCAGTGAGAAGGCT[A/G]CCTCCCCTCAGCCTG | 10533 |
| rs190730622 | snp | A/G/T | 0.00398731 | 0.0445001 | intron-variant | ATG7 | GRCh38.p7 | 3:11314522 | ATTGACTGCTGGCAG[A/G/T]TATGGGGTTTCTTTT | 10533 |
| rs190731116 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11538857 | ACATACTGGGCAACA[C/G]AGTGAGACTCTTGTC | 10533 |
| rs190733359 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373548 | TCAAGTTCCAGGGGC[G/T]TCTTCTGATGAGGCA | 10533 |
| rs190751022 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11498204 | TCTTTCTCTAGAATT[C/G]AGGCTGTAGTCTCCA | 10533 |
| rs190753905 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11514207 | GCCCAGGATGACAAA[C/T]GAAGGAAAGTGGTTG | 10533 |
| rs190768302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11478981 | TGAATATGTGCCTGT[A/T]TATTTACAACACACA | 10533 |
| rs190773720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538129 | CCACAGGGAACCTGA[C/T]GGAAGGTTGGTGGCA | 10533 |
| rs190776342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445018 | GAAATACATCTCACA[A/C]CAGTCAGAACGGCTA | 10533 |
| rs190790834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532368 | ACGGAGGAGGACAGA[A/G]CTGAGTCTGGAAAGA | 10533 |
| rs190796638 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11502838 | AAGAAGCAATTAGAT[A/C]CCCAGGCCCCCACCT | 10533 |
| rs190812041 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11465199 | CAGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 10533 |
| rs190837181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11431392 | CAAGGGCGGGGGGAA[A/G]AAAACAACCACACAC | 10533 |
| rs190885978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336087 | CTCTGTTGCCCAGAC[C/T]GGAGTGCAGTGGCAG | 10533 |
| rs190890191 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11302408 | CCTTTATTATTACCC[A/C]ATTTTTGTTTTGATT | 10533 |
| rs190891690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279853 | GTATTTGTTTTACCT[C/T]CAAATTGCTATACTC | 10533 |
| rs190898604 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11354753 | CCTAATGAGTAGTGG[A/G]TACTGGACTAGCTCT | 10533 |
| rs190908189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324600 | AGCCCATGTTAGGTC[A/G]GGTTGCTCTAAGAAA | 10533 |
| rs190913956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11392833 | GGTAGAAACTGGTAA[C/T]GTCCTATATTAGAAG | 10533 |
| rs190953875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314878 | CAGGAGGTCGAGGCT[G/T]CAGTGAGCTGTGATT | 10533 |
| rs190955768 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11284561 | CTTTTTTATTTTATT[A/T]TATTTTTTGAGACGG | 10533 |
| rs190975570 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358840 | CTTTTGAGATACTCT[A/C]CACTGAAAGATATAC | 10533 |
| rs190980516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11310695 | TGGAGTGCAATGGTG[C/T]GATGTCGGCTCACTG | 10533 |
| rs190985887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389792 | TCTGAACTCACCTGT[C/T]GTCATAAGTCTTGGC | 10533 |
| rs190989735 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529679 | CTTGATTTTTTTCTC[A/C]TAATTGAGGCTTCAC | 10533 |
| rs190991080 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11394077 | ATTTTATACACAAAT[C/T]GTTGTCCAGGGTCAT | 10533 |
| rs190999746 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11546913 | CACAGGCTGATGCCA[C/T]CCTCTCCCTAACTGT | 10533 |
| rs191002259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11553245 | GGCCAATTGCCTTAC[C/T]TCTCTGGGCTTGTTT | 10533 |
| rs191016146 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528804 | GCACTCCAGCATGGG[C/T]GACAGAGCAAGACTC | 10533 |
| rs191022591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11461252 | ACCCAAGGCCATTCT[A/G]TGTCCCTTAGGAAAT | 10533 |
| rs191029567 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516998 | TGAGGCAGGAGAGTC[A/G]CTTGAACCTGGGAGG | 10533 |
| rs191033956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513001 | CAAGTCCCCACCAGA[A/G]TAGCTAGATACAGAG | 10533 |
| rs191051282 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11491913 | GTTACTGCTGTCTTT[C/T]TGTTTGTCTGTGCCC | 10533 |
| rs191052309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306304 | GAACACATACTTTCT[A/G]TCCTCAAGGAGCTTA | 10533 |
| rs191056272 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329669 | TTATTTTGGGATAAT[A/T]TTAGATTTACAGAAG | 10533 |
| rs191058168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11456750 | GGAAAGAAGTAGACA[C/T]TTGTGAAGTTTTTTT | 10533 |
| rs191061629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484660 | ACCCATTAACTCATC[A/G]TTCAGCATTAGGTAT | 10533 |
| rs191076396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448138 | TCACCTAACCACAGA[C/T]ACCAGAAAAGAAGTC | 10533 |
| rs191079559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418686 | CTCTGTATCCACCTG[A/G]CTGTCTCTCCAGTTC | 10533 |
| rs191094742 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555457 | CAGACATGGCTTTCT[G/T]CCTCCCAGCCTGTCC | 10533 |
| rs191119084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539737 | AAATAAAATCTATTG[A/C]TGCGCATACAATCAA | 10533 |
| rs191124238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550644 | CTCAAGTGATCCTCC[C/T]GCCTCAGCCTCCCAA | 10533 |
| rs191128496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508917 | ACAAATTAATAACAA[A/C]TTAGATCTCTGCTCC | 10533 |
| rs191132086 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11379362 | TGAAACCTGATTATA[C/G]CTGATACTCTGGAAA | 10533 |
| rs191135457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522003 | AGTCCTGACGTAGCT[A/G]CCATTGTTATCTGCA | 10533 |
| rs191189539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11294836 | TAAGTGCTCAAAGGC[C/T]GGGAGCAGTGGCTCA | 10533 |
| rs191207346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289508 | GCAGCTCAACATCAA[A/C]TATATCCTCTTATGA | 10533 |
| rs191209427 | snp | C/T | 0.0165167 | 0.089362 | intron-variant | ATG7 | GRCh38.p7 | 3:11340638 | TTTGTGTTTTATTTG[C/T]CTTAAGATTGTCCTA | 10533 |
| rs191216501 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11337431 | TGCACTCCAGCCTGG[C/T]GAGACAGCAAGACTC | 10533 |
| rs191243456 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11490413 | ACACTGATGAGTCTT[G/T]ACTCTTTATCCAGTT | 10533 |
| rs191249969 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11471147 | TTGGAAACACACATA[C/T]GAATATGTTACTCAG | 10533 |
| rs191253544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11454819 | TCATCAAATGCTAAT[A/G]AGGTTAATGGCTACC | 10533 |
| rs191284853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450271 | GTGTTCTTAACTACT[A/G]CTTTGTAGTGTCTTT | 10533 |
| rs191286062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | ATG7 | GRCh38.p7 | 3:11510205 | TCTTTCTTTCATCCG[A/G]CCCAAGAATGGCACC | 10533 |
| rs191287795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474527 | CTCATCTGAGCACAG[A/G]ACTTGGAGGTTGCAG | 10533 |
| rs191294126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11430442 | GAATTCTGCATTCTA[C/T]GTAGAAAGGTCTCCA | 10533 |
| rs191301869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11411214 | GTTGAGCATCTTTTC[A/G]TGTGCTTATTGGCCA | 10533 |
| rs191303811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458159 | AGTTTCAAATTTAAA[C/T]TGGCTACTCAAAGCC | 10533 |
| rs191309128 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11551077 | TTTTCGTAATGAGCC[A/G]AGATGGCACTCCCCA | 10533 |
| rs191312096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436961 | TTCCTTTCGAGGTGA[C/T]GAAATGTTCTAATCT | 10533 |
| rs191322240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371020 | TTTCCTGAGCCTCCT[A/G]TGTTCCTATTTGGAG | 10533 |
| rs191325853 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11523758 | ATTATACCACACTTG[A/T]TCTCTGATTACGGCC | 10533 |
| rs191333053 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11353444 | TGAGACTCTGTCTCA[A/G]AAAAGAAAAAAGAAA | 10533 |
| rs191337084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11371964 | CAGCTGGGAACAGCC[C/T]GGGAGCGAGGCCAAA | 10533 |
| rs191343512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11406092 | CCTCCCAGGCTCAAG[C/T]GATCCTCTCACCTCA | 10533 |
| rs191347362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391210 | GGGCCTGGCCTCAAG[A/T]TGTGAGCAAATACTA | 10533 |
| rs191376745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466431 | TGCTTGGCAGAGACA[C/G]AAAACAGTCACTCAT | 10533 |
| rs191379286 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11291474 | GGTTATCATCTCAGC[C/T]CTACCACTTCCTGTG | 10533 |
| rs191390171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11344946 | GTCATGTTATTCCTT[G/T]TTCTATCTTTGTATA | 10533 |
| rs191394717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366269 | TCACTTAGCCTCCCA[C/G]AGTCTCAGTTTCCAA | 10533 |
| rs191404253 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11385601 | TGTTCAGTTGTGAAA[G/T]GCCCTACAGCAAGGT | 10533 |
| rs191418647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334094 | ATGTCCTATGTCAAA[A/G]TCAGAGCACGATGTC | 10533 |
| rs191450730 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11311290 | GACTTTTGAAAATGA[C/G]CTGATAAAGTTTCTT | 10533 |
| rs191461668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355557 | GGGGAAAAAAGCTTG[A/T]ACAGGTACTTAATTT | 10533 |
| rs191508199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447450 | CCAGCCCGGGCAACA[A/G]TGCAAGACTCCGTCT | 10533 |
| rs191522992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408307 | ACCACCTTAGCCTGG[A/G]CCTTGTTTATATCAC | 10533 |
| rs191528106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297902 | CTGTGTCGAAGAAGG[A/C]ATAACAGTAGTGCAT | 10533 |
| rs191534202 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11275444 | AGCTCTGCCTCCTGG[A/G]TTCACTCCATACTCC | 10533 |
| rs191535347 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11541218 | TTTAGCTTTTACATA[C/T]ATGTTTGTGATTGAT | 10533 |
| rs191545607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510784 | GGCTTGGGGTAGAAT[C/T]GATAGCTTAAAAGAT | 10533 |
| rs191580438 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507218 | ACCCAGGAGGCGGAA[C/G]TTTCAGTGAGCTAAG | 10533 |
| rs191598373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469760 | GGAGGCTGAGGCGGG[A/G]TAGATCATTTGAGTT | 10533 |
| rs191601681 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11528039 | TTGAAGATCACCCAC[A/G]TGTGGTCCCTTCTGC | 10533 |
| rs191606941 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556949 | CAAGAGCCAGTCCTC[C/T]GACCTTTTCACCCAG | 10533 |
| rs191618662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11540163 | TTTGCTGTTGCCACC[A/G]GCAGAGTTTGAGAGT | 10533 |
| rs191622737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11342489 | CCACACCCATCGCAA[G/T]TCCCATTTCCTATTA | 10533 |
| rs191623701 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433016 | CTGCATTTGGGATGG[A/C/G]TACAGTGGCTTACAC | 10533 |
| rs191625955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361175 | AGTTCTAAAAAGTCT[C/T]TTAGGTTCCCTCTAC | 10533 |
| rs191633885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382103 | AAGTAATTTTTTCCT[C/T]TGGTAGTTTTCAGTA | 10533 |
| rs191667396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402438 | ACTCCGTCTCAAAAA[A/T]TAAATTAAAAAAAGA | 10533 |
| rs191680400 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11277251 | TGTGGATTGCCTTTA[C/T]TAAAATAGAGATCTA | 10533 |
| rs191688014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319567 | CTCCCAAGTAATTCA[A/G]TTTTCTCTCACCGGC | 10533 |
| rs191698723 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11364834 | CCACTTCATATCCAC[C/T]CTACTTACCCTGCAG | 10533 |
| rs191729665 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11394348 | GCTCTCTTACTGAAG[C/T]CACCTTAAGAAACTG | 10533 |
| rs191750386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464066 | TGAAAAACAACAGGT[A/G]TAGTATGCTTTTGTA | 10533 |
| rs191754766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279061 | CTTCCTCCCTTTGCC[C/T]GGAGAGTCCCCACTC | 10533 |
| rs191770691 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11427361 | TGCCTGGCTTTTTCA[C/T]GATTTGATCAGTCTT | 10533 |
| rs191777918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11322550 | TTTTAATCCTGTGCA[C/T]TTTTTAAAACTAAGA | 10533 |
| rs191787081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486249 | TTCTCCTTGAAGAGG[C/T]CCTTCACTTCCCTTG | 10533 |
| rs191800582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467921 | GAATTAGAAAGAATT[A/C]CTCCCCCAGTGTCAT | 10533 |
| rs191805530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280715 | TCATTATCCAAGTTA[C/T]TGGTAAAATATGGTA | 10533 |
| rs191807308 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11524106 | CAGTTCAAAAGCAGC[G/T]TGAAATATTCTCTGT | 10533 |
| rs191820736 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270669 | TTTTGGGGGTAGGGG[A/G]TGGATCTCACAAAGT | 10533 |
| rs191821086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11325116 | AACAAGCTATACCAG[A/G]TAGCCCAGGTGTGGT | 10533 |
| rs191822607 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303759 | TCTTTCCCTTGAGGA[A/G]TATTTGTCTTTATTC | 10533 |
| rs191847486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11459722 | TGATAGCCTTTTGTC[A/G]AGGCAATAGCCATTC | 10533 |
| rs191851588 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11552414 | GAGGACATTCACTGT[C/G]CCCCTTCTCCACACC | 10533 |
| rs191857958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11344642 | GAGGCCAAGGTGGGC[A/G]GATCGTTTGAGCTCA | 10533 |
| rs191864329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537384 | TTGTCACCTCCACTA[A/G]GCAGGGACCTCCCAG | 10533 |
| rs191867505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423543 | CTTAATTTCAGTGGA[C/T]ATTTTTTCCTGACGT | 10533 |
| rs191872797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505310 | AGAAAAGAAGACTAG[C/T]GGTAAGCCAGGTGTA | 10533 |
| rs191873208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11518311 | CAGGACTTTGGGAGG[C/T]CAAGGTGGGTGGATC | 10533 |
| rs191875699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384709 | TCACACCTGTAATCC[C/G]AGCACTTTGTGGGGG | 10533 |
| rs191880529 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11546582 | AGAAGAACCTTAGTT[C/G]ATGGCATGCTTCAGG | 10533 |
| rs191889453 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512368 | GAGCCTGGTGCTGCA[A/G/T]CTTGGCCAAGGGAAC | 10533 |
| rs191894115 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11489176 | TTTCTTCTAGATTTT[C/T]CCAGCTGTATGCTGG | 10533 |
| rs191912425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452822 | TAGTGTTAAGACCTA[C/T]TCTTTTTAGTATTTT | 10533 |
| rs191985805 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11552029 | GCTGGGATTACAGGC[C/G]TGCGCCACCACGCCC | 10533 |
| rs191985950 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11511781 | AGAAATCGAGCACAG[C/T]ACCGGTGGGCTGGTA | 10533 |
| rs191993067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11296705 | CCCTCCACATGAGGA[C/T]AGCTGGTTTCACGTG | 10533 |
| rs191994306 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11493718 | ACTTAGATACAAAAA[A/C]CAAAAGTTTCCGTGA | 10533 |
| rs191995902 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11369429 | TTCCCTCCCTCCAGC[C/G]ATCCCCTCAACAGGT | 10533 |
| rs192000185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535529 | GGTGGTGACAGTGGG[A/T]CAGTAGCCCTGCCTG | 10533 |
| rs192003486 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11341267 | GGGTTTCACTGTGTT[A/G]CCCAGGCTGGACTCG | 10533 |
| rs192034151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11415146 | ACAACTATAACACAA[C/T]GGTAAGTACTTGTGT | 10533 |
| rs192044716 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11307916 | GTCGTTTTTCTTGAC[C/T]TGTGGCTTGACTGCT | 10533 |
| rs192051704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11332321 | TTTATGTAAAGTTAA[A/G]ATAGGCAAAACCAAT | 10533 |
| rs192053108 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11554318 | CTCTAGTGTGAGTTG[C/G]GAGTGTGGGCAGCTG | 10533 |
| rs192060897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382492 | GAAGGATGGTGGGGA[A/G]AGGTGGGTGGTGAGG | 10533 |
| rs192062007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302202 | TGGCTAATTAACTGT[C/G]CTACTTCAATAAGCT | 10533 |
| rs192082889 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344392 | GTAAGTGTTCTTTAT[A/C]ATTTAAAGAAGCTGA | 10533 |
| rs192112427 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475949 | GAGTTTCCTAACAGT[A/G]CAGTTGTCCTGTCTG | 10533 |
| rs192116778 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11458515 | TGATCCGCCCGCCTC[A/G]GCATCCCAAAGTGCC | 10533 |
| rs192118539 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11517792 | GAGCTGGAGAGAGTC[A/G]GGCAATTGAGTTGAA | 10533 |
| rs192130941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11441119 | GGGATATTTTTGTTT[C/T]GTTATAATTTGCTGC | 10533 |
| rs192137265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422048 | TTGTTGTTTCGGTTA[C/T]AGAGCACAGGCAGAG | 10533 |
| rs192142055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548890 | ACTCCTAAAAGTGAG[A/G]CGGCCGGGTCAAAAG | 10533 |
| rs192145249 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11402989 | AACCAGGAATCTATT[A/C]TCTTAAATGCTTAAA | 10533 |
| rs192151465 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515787 | TCCTCAAAGAGTGTA[A/G]GTACAGTTTAATGGG | 10533 |
| rs192161647 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11480153 | AGCCAGCATGGTCTC[A/G]ATCTCCTGACCTCGA | 10533 |
| rs192165748 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11462526 | CTTTAGGGTTGGCTA[A/G]TTTGAATAATCTCAG | 10533 |
| rs192166829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11444254 | AGTGTGCTGTTTGGA[A/G]CATTCTGGTATATAT | 10533 |
| rs192169728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11445125 | TAAATTAGTTAAATC[A/G]TTGTAGAAAGCAGTG | 10533 |
| rs192175153 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11365892 | ATTTTGCTTCCTGTT[G/T]GTACCCCAGCCCCCT | 10533 |
| rs192181108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405905 | ATTATAGGCATGATG[C/T]CTGTAATCCCACTGC | 10533 |
| rs192181963 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11425029 | GTGCAGTGGTGTGAT[A/C]ATAACTAGTTGCAGC | 10533 |
| rs192190614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406498 | AAATTTGTAGAGATG[A/C]CATCTTGCTATATTG | 10533 |
| rs192214832 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288192 | CATCCAATATATGCT[C/T]GAACACTTCTGCTAA | 10533 |
| rs192237724 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11515130 | AGGCATGAGCCACCG[C/T]GCCTGGCCTAGGTTT | 10533 |
| rs192287574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11339170 | GCATGCTGGCGGGCG[C/T]GTGTACTCCCAGCTA | 10533 |
| rs192290245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11289748 | CTTTTTTTGTAGAAA[C/T]GGGGTCTCACCATGT | 10533 |
| rs192298557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11356511 | TGGACATAACTGATG[A/G]GCTCTAACGTTAGCT | 10533 |
| rs192305345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11304843 | ATTCTTTTTAGGAGC[C/T]ATGTTGAGATATAAT | 10533 |
| rs192305522 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11326646 | ATGTGAAGTTGAAGC[A/G]ACGATTGCTAAATAA | 10533 |
| rs192306761 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11376630 | GCTTAGCAGTTGTAC[A/G]GAGTCTGTAAAAAAA | 10533 |
| rs192306863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416574 | TAATAAAGGAATACT[A/T]TCACTAAAAAGTGAT | 10533 |
| rs192308601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375868 | GGCCAAGATTTTAAT[A/G]TGATGTGGTCACTTT | 10533 |
| rs192308764 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11274890 | TGGGGGCGGGGGTGG[A/G]GAGCAGGACACTGAA | 10533 |
| rs192311938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11346661 | GCACGTTCCCAGAGT[A/G]CCTTCCTTGCTATCC | 10533 |
| rs192318430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394825 | AGAGGGAAATATGAT[A/C]CTAGTCCTAAAATTA | 10533 |
| rs192327410 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11349645 | CATTATGAGTTTAAG[A/T]TGAGGAATTTAGGAG | 10533 |
| rs192335994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317009 | CCCACCTCCCCTTTT[C/T]TGTTGTATTTTTATT | 10533 |
| rs192345285 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389110 | AAAATTAGCCACACT[C/T]GTAATCCCAGCTACT | 10533 |
| rs192347955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454020 | CCACTTCAAACCTCA[A/G]TCTTGCTAAACTGAG | 10533 |
| rs192350976 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11438735 | GCATTTGCTGGGTAG[A/G]AGAGGTTTTTCAAGA | 10533 |
| rs192358902 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433613 | CCTAAGTCCCTTTAC[A/C]CAATTTCCCTGAAAT | 10533 |
| rs192367317 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11415899 | GTACGTGGTACACTT[C/T]TATGCTACGGGCAGC | 10533 |
| rs192369681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401419 | TTTAAAAAGATGACC[A/G]AGAATAGAAAGTTGT | 10533 |
| rs192373630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536542 | GTTTCCCATGCAAAA[C/T]GCCACCACACACCTA | 10533 |
| rs192394566 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11281729 | CAGTGAGCCGAGATC[A/G]TGCCATTGCACTCTA | 10533 |
| rs192403284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11539247 | CTACGAGGGAGACAG[C/T]ATTTTTGTCCTCATT | 10533 |
| rs192405043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504607 | AGATTGTGTTAAGAT[C/G]AAATGGCTTGAATAC | 10533 |
| rs192431746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11318613 | TCATGTAACTCTTCT[A/G]CTTAAAACCCTTCTA | 10533 |
| rs192455397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360964 | CTGGCGTCATCAACT[A/G]TACACCTGTTCCTTG | 10533 |
| rs192536628 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285932 | GTCCCCAGCTGTCAC[A/G]TCTTTGTGGTCTCTT | 10533 |
| rs192541494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530599 | TCTGAGACCAACCGC[A/T]GTTGCCCTCCTGACC | 10533 |
| rs192577186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11421524 | CAGTCACATCTTCAG[A/G]CTCCACTTTTAGTTC | 10533 |
| rs192599979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11501027 | TGGGAAGCCAAGGTG[C/T]GAGGATCACTTGAGG | 10533 |
| rs192600175 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11515491 | GTATTTTTAGTAGAG[A/G]CGGGGTTTTGCTGTG | 10533 |
| rs192611823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11351512 | AAAGAAGATGAGGAG[A/G]AAGAGAAGGCTGAGG | 10533 |
| rs192632130 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11395749 | ATCGAGACCATCCTG[G/T]CTAACACGGTGAAAC | 10533 |
| rs192650841 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11470481 | GGGGCCACCCTCATA[C/T]GTGCAGTCCATTGTT | 10533 |
| rs192692649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11530572 | GACTTGATGGTGAAA[G/T]GAATCCCCTCCTCTG | 10533 |
| rs192693982 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11312913 | CCATCTTTTTTGTTG[C/T]TGTTTAGGTTTTTTA | 10533 |
| rs192706381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11434239 | ACAGTCAGATATTTA[C/T]GTACAGCTTCATCAA | 10533 |
| rs192735801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421072 | AAAATACTTTTTTTT[C/T]GCTAAAAAATGCTAA | 10533 |
| rs192745087 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11552148 | TTACTAAATACTTTT[C/T]CATTTGTATTCTAAG | 10533 |
| rs192749780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518093 | AGAGGAAGGGGACCA[A/G]GGTGCTTCCCTGGGG | 10533 |
| rs192756642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11525277 | CTCAGGTGATCTACC[C/T]GCCTTGACCTCCCAA | 10533 |
| rs192763704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492925 | GCATGTTACAATGCT[C/G]TCTTAGCTCCGCCGT | 10533 |
| rs192773821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458327 | GGAGTGCAGCGGCAC[A/C]ATCTCCGCTCACTGC | 10533 |
| rs192779603 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11341446 | CTCAGTGCACTCTTT[C/T]TTTTTTTTCTTTTTT | 10533 |
| rs192782873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11308902 | AGAAGAGCCTGGTGC[C/T]TTTCAGCTCCACACT | 10533 |
| rs192787608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11380633 | GTTTTAATAGGCTTT[C/T]GGATACCATCTGAGT | 10533 |
| rs192813726 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11544408 | CAGAGCACCCTTTTT[A/C]TGACCAGCCCCAATC | 10533 |
| rs192849549 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11285265 | GCTCACTGCAGACTC[A/G]ACCTCCTGGGTTCAA | 10533 |
| rs192855123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410930 | GGTGTATAGCCAGAA[A/T]TGAATTGCTGGATTC | 10533 |
| rs192890848 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485471 | AGTAGGTTGTGAAAA[A/T]TTTCTCCCATTTTGT | 10533 |
| rs192893414 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371367 | ACAGCGAGTAAAGGG[G/T]CACAGCGGAGAAGGC | 10533 |
| rs192894341 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11449533 | TTTAGTTAGTATACA[A/G]AGAAGCTTCTCATGT | 10533 |
| rs192894571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343220 | AGGTGTGAGCCACCA[C/T]GCCTGGCCAAACATG | 10533 |
| rs192903389 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11435063 | TTAGTGATTTTGATT[C/G]AAATATACCATGTAT | 10533 |
| rs192935710 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530038 | AGGACCTTCTACTTG[C/G/T]ATCAGAGGTGTCGTT | 10533 |
| rs192939012 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509368 | GGGAGCTGTTTTTTT[C/T]CTGATGCAACATGAA | 10533 |
| rs192945003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471690 | TCTCACATATTCCAA[C/T]TCTTTTTTTTTTTAG | 10533 |
| rs192955167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281192 | CCTCATACAGTTATG[C/T]AGGCTGTGCACTGCA | 10533 |
| rs192965414 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325896 | TTTAATAGCCTTTGT[A/G]TGTTTTTTGTTGTTG | 10533 |
| rs192971476 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11511582 | GCTGCCTGCCAGTCC[C/T]GTACTGTGCGCTCAC | 10533 |
| rs192976767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366636 | TTAATTAAATTTTCA[A/G]TCATGCCCCTGCACT | 10533 |
| rs192980260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475714 | GTCAGAAAAATGTCC[C/T]AGTGTCAGAATTGAA | 10533 |
| rs192985446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11439349 | GCTGGGATTACAGGT[A/G]TGAGCCACTGCACCG | 10533 |
| rs193006151 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11544041 | GTCTGCCTGCTCCCT[G/T]CCCTCTTGGTTCACT | 10533 |
| rs193019584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386902 | TATTTAGCTACAAGC[C/G]TTAACCTCAGAACTC | 10533 |
| rs193028152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525881 | TTTTAAATCAAAAGA[C/G]CACTAGCAGCTGCTG | 10533 |
| rs193043600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312233 | TTAATTCTTAGCAAG[A/G]TTCAAGAAGAAATAT | 10533 |
| rs193084916 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11503673 | AGGCAGGAGAATCGC[C/T]GGAACCCAGGAGGCG | 10533 |
| rs193112650 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350926 | GAGACCCTAGCCCAA[A/G]AAAAAAAAAAAAAAA | 10533 |
| rs193128486 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11465691 | GATTGCTTGAACCCA[A/G]GAGGTCGTGGCTGCA | 10533 |
| rs193130723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521908 | TGACTCTAGACTGCC[A/G]CCGCTGCCGACAACA | 10533 |
| rs193132084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462687 | TGTCAGAAGTGTACT[A/C]CTGGCTGGGCCCTTT | 10533 |
| rs193133006 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11489518 | TCTTGCCTTCTGCTG[A/G]CTTTTGAATGTGTTT | 10533 |
| rs193136899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425190 | GTTGGTCCTGAACTC[C/T]TAAGCTCAAGCAGTC | 10533 |
| rs193146516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390440 | TAATATTCCAATAGG[C/T]GCTGAAAGTATACCT | 10533 |
| rs193153540 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11362089 | GCTGGTCTTGTTATT[C/T]AGTGATTGTCAACAA | 10533 |
| rs193153805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429481 | AGCCTGGGCGACAGA[A/G]CGAGACTCCATCTCA | 10533 |
| rs193157668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11417470 | GAAGTCTGTTCTATC[C/T]GAAATTAATTCAGAT | 10533 |
| rs193168632 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11386398 | AATATATATGTATGT[A/G]TATAGGTATACATAG | 10533 |
| rs193168702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522489 | GAGCGGATGAGCCTC[A/T]TACTGTGCACAGTTC | 10533 |
| rs193172711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11548674 | CACTAAAGAAATCCC[A/G]GAACTGAGCCCCCGT | 10533 |
| rs193176932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455187 | GCCTAGAAACTAAAG[C/T]AGTGTAGAATGCCTT | 10533 |
| rs193183121 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11304232 | GTGTGTGGGGCAGAG[A/G]CTGTGTCTTTCTTAT | 10533 |
| rs193189946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11346046 | TCATTAAAAATGATG[C/T]CTGTCTATGAGGCCT | 10533 |
| rs193210333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366875 | TAGTTCTTTCTCCTC[A/G]TTTTCAAATGTCTGA | 10533 |
| rs193217684 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11406992 | AATCATGTCTTCCCA[A/G]CAGTCCCCCAAAGTC | 10533 |
| rs193224860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290549 | CTTCTCCTCCAGGTA[A/G]CTGTCACTGCCTGGT | 10533 |
| rs193228294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11338766 | CTTCTTGCTGTGAAT[A/G]ATACCCTCAGCCAAA | 10533 |
| rs193281698 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11480380 | TGTCTCTACAAAAAC[A/T]TTTAAGATTGGCTGG | 10533 |
| rs193285978 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11507632 | TAAAGTTATGGGTGT[C/T]TTTTGTTTTTGTTTT | 10533 |
| rs193288210 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11445805 | CCTTATCCTTGCCAG[A/T]ATCTTGGTACTGTCA | 10533 |
| rs199507551 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11388194 | GACTCCTTTTCCTCA[A/C/G]CTGTAGTAAAGGGAG | 10533 |
| rs199515034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11451762 | CATAGAAAATATTAC[A/G]TGTATATATATGTTT | 10533 |
| rs199548086 | snp | C/T | 0.000264901 | 0.0115057 | intron-variant | ATG7 | GRCh38.p7 | 3:11307093 | GATGTATGTGTCATA[C/T]TTCCTGTGGTCCTGG | 10533 |
| rs199548802 | snp | C/T | 1.65119e-05 | 0.00287327 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347896 | GGGGCGTGAGACACA[C/T]CACATTTGTGGACAA | 10533 |
| rs199549305 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295775 | TTTCTTTCTTTCTTT[C/T]CTTTCTTTCTTTCTT | 10533 |
| rs199563778 | in-del | -/AGTG | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11283278 | AGAGGAAATTTTCAT[-/AGTG]AGCATGGGGAAGGGG | 10533 |
| rs199567042 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468315 | GGGGTAAGTGGAGCT[-/C]AGTGGGAGAGCACAG | 10533 |
| rs199567151 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11274595 | CTGGAAAGGTAAGCA[A/G]TAGCCACATCGTGAA | 10533 |
| rs199573059 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487257 | ACAGACACGGCAACC[A/G]TCCGATTTCTCAATC | 10533 |
| rs199590485 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451886 | ACACACACACACACA[C/G]ACACACACACACACA | 10533 |
| rs199592825 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486133 | TAAATTACCTTGGGC[A/T]GTATGGCCATTTTCA | 10533 |
| rs199593182 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298928 | TATAGTGTCAGCTTT[C/T]CTTTAGAAAGAGACA | 10533 |
| rs199597841 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490516 | TGATCCTGTCATTAT[G/T]ATGTTAGCTGGTTAT | 10533 |
| rs199605104 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11437726 | TGCATGCACTCCCCC[A/G]ACGTCTTATCACAGT | 10533 |
| rs199607021 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516047 | AAAAAAAAAAAAAAA[A/C]AAAAAAACATAGGAC | 10533 |
| rs199612628 | snp | G/T | 0.216349 | 0.247725 | intron-variant | ATG7 | GRCh38.p7 | 3:11395968 | AAAAAAAAAAAAAGG[G/T]AGGGGGGGAAGAGTA | 10533 |
| rs199617802 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382277 | ATACATTATATACAC[-/AT]ATATATATAGAGAGA | 10533 |
| rs199639266 | in-del | -/AATG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413595 | AAAACTGACTTAATA[-/AATG]AATTCAGCAAAGTAG | 10533 |
| rs199650130 | snp | A/G | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527069 | TGTGTGTGTGTGTGT[A/G]TGTATATATATATAT | 10533 |
| rs199666239 | in-del | -/GCC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277900 | TATAGACCCCCCCCC[-/GCC]CCCCACCAGGAATGC | 10533 |
| rs199667100 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11418967 | TGGGAAACTGCCCCT[-/C]CCCCCCCGATCCAGT | 10533 |
| rs199691725 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11299385 | GCTGGGCTGCCAGCT[C/T]GCTTAACATTGGAGT | 10533 |
| rs199731819 | in-del | -/C | 0.031825 | 0.122064 | intron-variant | ATG7 | GRCh38.p7 | 3:11388434 | CTCATGTTCCTTCTT[-/C]TTTTTTTTTTTTTTT | 10533 |
| rs199737137 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306978 | GTTGCTGCCCAGCTA[C/T]TGGAACACTGTATAA | 10533 |
| rs199773599 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | ATG7 | GRCh38.p7 | 3:11480580 | TTTCAAGAAACAGAC[-/A]AAAAAAACCTTACAA | 10533 |
| rs199779793 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487490 | ACCTCCCTCCCGGAC[A/G]GGGCGGCTGGCCGGG | 10533 |
| rs199794330 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295814 | TTTTTGAGATGGAGT[C/T]TCGCTCTTGTTGCCC | 10533 |
| rs199804502 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465003 | TCGTCATCAACAATC[A/C]CAGCCTTATTAAAGA | 10533 |
| rs199845662 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372865 | GCGTGTGTGTGTGTG[A/T]AATCGGCCATGTTTT | 10533 |
| rs199851494 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11524805 | AACAAAAACAAAAAC[-/A]AAAAAAAAACAAAAC | 10533 |
| rs199871405 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342229 | GTGTCTGTCAAATGT[C/G]TGCTGCTTGGAGCCG | 10533 |
| rs199881053 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491276 | CATTGGCTCCTGAGG[C/G]TTCTGCATTCTTCAC | 10533 |
| rs199886832 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397387 | ATTCACCAGGTAGAA[A/T]TTCTAAATTTGTATG | 10533 |
| rs199892649 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273227 | TCATATCTGTGGCTG[G/T]CAGTTTGGGACCTCT | 10533 |
| rs199899189 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412010 | ACACCAGGGTATTCT[A/G]TCTAGGTCCTGCTGC | 10533 |
| rs199901094 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11521557 | AGGAAGGGTTTTTTT[G/T]TTTTTTTTTTTTTAA | 10533 |
| rs199926572 | snp | A/G | 0.00199802 | 0.0315439 | intron-variant | ATG7 | GRCh38.p7 | 3:11358408 | TAACTACGTCCTGGT[A/G]TTTCCCTAGAATGCC | 10533 |
| rs199927820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315325 | TTCTAGAGAATAACA[A/G]CGTGTTTTCTGTTTT | 10533 |
| rs199941131 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390760 | TTTTTAAAAAACTGC[A/T]AGTTAAAGTACTGCA | 10533 |
| rs199954389 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11522476 | TTATTAGTGAGATGA[-/G]CGGATGAGCCTCATA | 10533 |
| rs199965055 | in-del | -/ATCC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538588 | GGGCTCACACCTGTA[-/ATCC]CAGCACTTTGGGAGG | 10533 |
| rs199965424 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539522 | AAATAAGACCTCTAA[A/C]TAAATGAGTGGGAGA | 10533 |
| rs199974104 | snp | A/T | 4.87021e-05 | 0.00493444 | intron-variant | ATG7 | GRCh38.p7 | 3:11315535 | ATTATATAGTTTTTT[A/T]AAAAATCTGAAGTTC | 10533 |
| rs199989952 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496977 | CTGCCTCAGCCTCCT[G/T]AGGAGCTGGGATTAC | 10533 |
| rs199990533 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396723 | AGAGGTGAAAGTTGC[A/G]GTGAGCCGAGATGGC | 10533 |
| rs199991390 | in-del | -/ATGAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413596 | AAACTGACTTAATAA[-/ATGAA]TTCAGCAAAGTAGCA | 10533 |
| rs199991529 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11369941 | ACATTCAGTATCTCA[-/T]TTTTACAAAACCAGT | 10533 |
| rs199999326 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288024 | TTTTTTAAGGGTTGT[-/A]AAAAAAAATAAAATA | 10533 |
| rs200018619 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487925 | GTCTCCTCACTTCTC[-/A]AGACGGGGCAGCCGG | 10533 |
| rs200042997 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490588 | TCTTTACAATTTGGC[A/C]TGATTTTGCAGTGGC | 10533 |
| rs200043617 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453167 | TCAATGTTGAGGGGG[C/T]TGAGAGTTCTCTGGG | 10533 |
| rs200058700 | in-del | -/TGT | 0.000141854 | 0.00842062 | intron-variant, cds-indel | ATG7 | GRCh38.p7 | 3:11510335 | TGAATGTATAATTTG[-/TGT]TATTACCTCTTATTT | 10533 |
| rs200064121 | in-del | -/T | 0.0693013 | 0.172766 | intron-variant | ATG7 | GRCh38.p7 | 3:11329963 | TCTTTGATTTTTTTT[-/T]GATGACCTTGACATT | 10533 |
| rs200074409 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533586 | ACTTGAAAGCAGAAA[-/C]TCTTCTCTGAAATCT | 10533 |
| rs200074530 | snp | A/G | 3.31022e-05 | 0.00406817 | splice-acceptor-variant, intron-variant | ATG7 | GRCh38.p7 | 3:11554809 | TCCCCTTCTCCATGC[A/G]GATCTGGGACATGAG | 10533 |
| rs200078175 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368256 | AAAAAAAAAAAAGAA[C/T]AAGAAGAAGAAGGAA | 10533 |
| rs200102879 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376638 | TTGTACAGAGTCTGT[-/A]AAAAAAAAATTCAAT | 10533 |
| rs200110966 | snp | A/C | | | intron-variant, missense | ATG7 | GRCh38.p7 | 3:11450201 | CATGGAACCTAAGTG[A/C]TCAAGGTCATGGAGC | 10533 |
| rs200120811 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336208 | ATGGCTATTTTTTTT[-/G]TATTTTAGTAGAGAC | 10533 |
| rs200126211 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417806 | ATTATTATTATTTTA[A/T]TTTATTTTATTTTTT | 10533 |
| rs200145868 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451833 | GCTGCCCTGTCTCTC[-/TA]TCTATCTCTCTCTCT | 10533 |
| rs200178132 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11281777 | GAAACTCCATCTCAA[A/G]AAAAAAAAAAAAAAG | 10533 |
| rs200180195 | in-del | -/TGA | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11535623 | AGCAGTGGACTTGAC[-/TGA]TGATTGACAGATGAG | 10533 |
| rs200182038 | in-del | -/T/TTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423470 | TGCCACAACTTTCAA[-/T/TTT]TTTTTTTTTCTTTTG | 10533 |
| rs200218448 | in-del | -/T | 0.135484 | 0.22223 | intron-variant | ATG7 | GRCh38.p7 | 3:11375038 | GAGACCTCATCTCTC[-/T]TAAAAAAAAAAAAAA | 10533 |
| rs200230728 | in-del | -/CTTGGGGG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452013 | CATGGTCACCAGGGA[-/CTTGGGGG]GTTGGGGGGTTGTGG | 10533 |
| rs200239712 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459190 | AAAAAAAAAAAAAAA[G/T]AGCAAAAACATCAGT | 10533 |
| rs200250775 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295776 | TTCTTTCTTTCTTTT[C/T]TTTCTTTCTTTCTTT | 10533 |
| rs200258266 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322227 | CACACATACACATAA[-/C]AAAACAAGACTTTTG | 10533 |
| rs200259863 | snp | A/G | 0.000758212 | 0.0194559 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347913 | ACATTTGTGGACAAT[A/G]CCAAGATCTCCTACT | 10533 |
| rs200268271 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317580 | CTATGCCCTTTCTTT[C/T]TTTCTTTTTTTTTTT | 10533 |
| rs200274860 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540488 | TATAAAAAATAAAAA[A/T]AAATTCACTGGGCAT | 10533 |
| rs200277509 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11443339 | GCTGAGGGGCAAAGG[A/G]GATTATATAAATGAA | 10533 |
| rs200282386 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484790 | TGAGTGAGAATATGC[A/G]GTGTTTGGTTTTTTG | 10533 |
| rs200289713 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465262 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 10533 |
| rs200294931 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489029 | CTGTGAATCCATCTG[A/G]TCCTGGACTCTTTTT | 10533 |
| rs200301332 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499265 | ACATTCCTCTATCCT[G/T]TCCTGTTCTACATGG | 10533 |
| rs200322219 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11275408 | GGCTGGAGTGCAGTG[C/G]CACGATCTCGGCTCA | 10533 |
| rs200327606 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486842 | TTTTTTTTTTTTTTA[A/T]TTTATTTTTTTATTG | 10533 |
| rs200342970 | in-del | -/TTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525032 | CTGTGCAAATCTCAC[-/TTTA]TTTATTTATTTATTT | 10533 |
| rs200346766 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294249 | TTATTTTATTTTATT[A/T]TTTTTTGAAATGGAG | 10533 |
| rs200350728 | snp | C/T | 0.000148252 | 0.00860837 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298732 | CCTGGACTCTCTAAA[C/T]TGCAGTTTGCCCCTT | 10533 |
| rs200351973 | snp | C/T | 0.000109308 | 0.00739201 | intron-variant | ATG7 | GRCh38.p7 | 3:11340764 | GCTGTTTTCTCCAGT[C/T]GGGCTTTTTGTAACC | 10533 |
| rs200360656 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11439072 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTG | 10533 |
| rs200364263 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417805 | ATTATTATTATTTTA[-/T]TTTTATTTTATTTTT | 10533 |
| rs200366506 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503459 | AAAAATGCTATTAAC[-/A]AAAAAAAAGGATATT | 10533 |
| rs200369595 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451800 | CAAAAAAAAAAAAAA[A/C]AAATTAAAAAAACCC | 10533 |
| rs200374109 | in-del | -/CTGTGC | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11284837 | TACAAGTGTGAGCCA[-/CTGTGC]CTGTGCCTGGCCTTT | 10533 |
| rs200382567 | in-del | -/GTTA | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11417323 | TCTTCTTGCCGTACT[-/GTTA]GTTTTTACCTCATGT | 10533 |
| rs200383178 | in-del | -/GAGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495453 | GGAGACAGGCTGGCA[-/GAGA]CCCCCAGACATCTTG | 10533 |
| rs200412655 | in-del | -/TTTATTTATTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462842 | CTCCTCTCAGATATT[-/TTTATTTATTTA]TTTATTTATTTATTT | 10533 |
| rs200419809 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485699 | TTAAGTCTTTAATCC[A/G]TCTTGAATTAATTTT | 10533 |
| rs200428870 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11383997 | GATATTAGTGTTTTT[-/C]CATCACTCCAGAAAG | 10533 |
| rs200432443 | in-del | -/T | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11391967 | CTTATTGGGGGGGGG[-/T]GTAATTTCACTTTAA | 10533 |
| rs200451856 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295791 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTGAG | 10533 |
| rs200468956 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397443 | TATAAAAAATTTACA[A/G]GAACTACCAGAAATA | 10533 |
| rs200477112 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406007 | TTGTTTTTGTTTTTT[G/T]TAGATGGAATCTCAC | 10533 |
| rs200477459 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462849 | CAGATATTTTTATTT[A/T]TTTATTTATTTATTT | 10533 |
| rs200493134 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445583 | ACTAATGGGCACCAG[A/G]CCTAATACCTGGGTG | 10533 |
| rs200504673 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507952 | AACCTTGCTGGTAAT[A/T]AAAAAAAAAACAAAA | 10533 |
| rs200507249 | snp | A/G/T | 1.70041e-05 | 0.00291577 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362903 | GCCGTGGAATTGATG[A/G/T]TATCTGTTTTGCAGC | 10533 |
| rs200532573 | in-del | -/TTG | 0.268995 | 0.249277 | intron-variant | ATG7 | GRCh38.p7 | 3:11471760 | CTTTTTTTTTTTTTT[-/TTG]AAATGTAGTCTCTAT | 10533 |
| rs200539119 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390093 | TGTTGAAACCTCCTA[C/T]GTATCCCAAATGTGG | 10533 |
| rs200539945 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409790 | CTTTTTTTTTTTTTT[A/G]CATGTGGTTGTCCAG | 10533 |
| rs200554907 | snp | A/G | 6.61759e-05 | 0.00575183 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11348010 | TGGCAGCAGCGGACC[A/G]GCTCCAGAAAATATT | 10533 |
| rs200558106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542320 | GGTGCCAAATATAGC[G/T]GGACCCTGAGGTCCA | 10533 |
| rs200579037 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400839 | CATTACAAACGTCAC[C/T]CAGGGTAATAATTTT | 10533 |
| rs200590021 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471746 | GGCTTTTTAGATTTC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs200595343 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357520 | AGTTAGCAAGTAGAG[-/T]TTTTTTGTATTTGAG | 10533 |
| rs200605522 | in-del | -/T | 0.0693013 | 0.172766 | intron-variant | ATG7 | GRCh38.p7 | 3:11315266 | AGGTACCTTTTTTTT[-/T]GAGTTAGTTTTTAGC | 10533 |
| rs200625429 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553405 | ATGGGAGAGTGAAAG[A/G]ATGGATGGATTGTGC | 10533 |
| rs200661669 | snp | C/T | 6.61081e-05 | 0.00574888 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11348004 | AGGCTCTGGCAGCAG[C/T]GGACCGGCTCCAGAA | 10533 |
| rs200664636 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279952 | GTTTTTTTTTTTTTT[-/T]GCCATTGAACCCTGA | 10533 |
| rs200673284 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519541 | GGCAGTGAGAGGAGT[G/T]TTTTTTTTTTTTTTT | 10533 |
| rs200683778 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11547552 | GGACTGGAATTGTTG[A/T]ACCATATGGTAACTG | 10533 |
| rs200686371 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487380 | GGGTGGTGGCCGGGC[A/T]GAGGGGCTCCTCACT | 10533 |
| rs200695341 | in-del | -/AAAC | 0.0825414 | 0.185628 | intron-variant | ATG7 | GRCh38.p7 | 3:11484402 | TCTCAAAAAATGAAA[-/AAAC]AAACAAACAAAAAAA | 10533 |
| rs200704465 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417803 | ATTATTATTATTATT[A/T]TATTTTATTTTATTT | 10533 |
| rs200705180 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11486134 | AAATTACCTTGGGCA[A/C/G]TATGGCCATTTTCAT | 10533 |
| rs200727974 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438599 | ATAAAGATTTTTTTT[C/T]TTTTTAACCTAAATT | 10533 |
| rs200733241 | snp | G/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11446964 | AAGTCAGTGGTGTTT[G/T]TTAGTGTCCGTCTGT | 10533 |
| rs200755603 | snp | C/T | 0.000103329 | 0.00718706 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554878 | TGACTTCTCCCCGGC[C/T]GCCTGCTGAGGAGCT | 10533 |
| rs200767609 | in-del | -/TA | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11382646 | AAATTCCAAGCTAAC[-/TA]TAGAGTATTGTGGTG | 10533 |
| rs200786439 | snp | C/T | 0.000235702 | 0.0108534 | intron-variant | ATG7 | GRCh38.p7 | 3:11313443 | CAAATAACCAAAATG[C/T]ACATAAAATTGGGTT | 10533 |
| rs200798032 | in-del | -/TTTATTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462842 | CTCCTCTCAGATATT[-/TTTATTTA]TTTATTTATTTATTT | 10533 |
| rs200799575 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441367 | CTACCTCAACCTCCC[-/G]AATAGCTGGGATTAC | 10533 |
| rs200808403 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507950 | GAACCTTGCTGGTAA[-/T]TTAAAAAAAAAACAA | 10533 |
| rs200833762 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451766 | GAAAATATTACGTGT[A/G]TATATATGTTTATAG | 10533 |
| rs200850584 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349239 | TAGACAGAAAAGTTC[C/T]CCCAAGTCCCCACTC | 10533 |
| rs200854890 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11324647 | CTGCTCAAAAAAAGA[-/T]TTTTTTTTTCACTAT | 10533 |
| rs200857476 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11521558 | GGAAGGGTTTTTTTG[G/T]TTTTTTTTTTTTAAG | 10533 |
| rs200922177 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540489 | ATAAAAAATAAAAAT[A/T]AATTCACTGGGCATG | 10533 |
| rs200934570 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506952 | TTACAGAGTGACAAA[-/G]GCTAGGGACCACTTC | 10533 |
| rs200946446 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459183 | ACTTTAAAAAAAAAA[-/C]AAAAAACAGCAAAAA | 10533 |
| rs200951717 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440518 | TTTAGTAGAGACGGG[G/T]TTTCACCGTTTTAGC | 10533 |
| rs200954370 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412280 | TTTTTTTTTTTTTTA[-/G]TAGGCCTGAAGGTCC | 10533 |
| rs200955300 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487513 | TGGCCGGGCAGAGGG[G/T]CTCCTCACTTCCCAG | 10533 |
| rs200979275 | in-del | -/ATG | 0.030665 | 0.119967 | intron-variant | ATG7 | GRCh38.p7 | 3:11547453 | CCACGTTTAACTTTT[-/ATG]AATACTTTCCTATGA | 10533 |
| rs200980786 | snp | A/T | 3.30322e-05 | 0.00406387 | intron-variant | ATG7 | GRCh38.p7 | 3:11306933 | CTAACCGTGTTTCTC[A/T]TGTATCTAGGAGTGC | 10533 |
| rs201011541 | snp | C/G | 0.00199799 | 0.0315437 | intron-variant | ATG7 | GRCh38.p7 | 3:11342093 | CAGAACAAGATTATT[C/G]CATAAAGGAGTGACT | 10533 |
| rs201043661 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372835 | GCGTGTGCGTGTGTG[C/T]GCGTGCGTGCGTGTG | 10533 |
| rs201056797 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400841 | TTACAAACGTCACTC[A/G]GGGTAATAATTTTCT | 10533 |
| rs201058224 | in-del | -/G/GG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396116 | TAAATCAGAAGTATA[-/G/GG]GGAAAAAAAAAAAAG | 10533 |
| rs201068773 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489131 | CCTGGTTTAGTCTTG[A/G]GAGGGTGTATGTGTC | 10533 |
| rs201101842 | in-del | -/TA | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527036 | ATATATGTGTGTGTG[-/TA]TATATGTGTGTGTGT | 10533 |
| rs201145510 | in-del | -/TCTTCTCTGAAA | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11533586 | CTTGAAAGCAGAAAC[-/TCTTCTCTGAAA]TCTTCTCTGAAATCT | 10533 |
| rs201154700 | in-del | -/CTATGCCTGG | 0.0298908 | 0.118541 | intron-variant | ATG7 | GRCh38.p7 | 3:11550549 | TACAGACACATGCCA[-/CTATGCCTGG]CTCATTTTTAAAAAA | 10533 |
| rs201157896 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11453203 | AGGTGGAGAACAGAC[-/G]GGGGGGCGTGGGCCT | 10533 |
| rs201173875 | snp | G/T | | | intron-variant, missense | ATG7 | GRCh38.p7 | 3:11450200 | ACATGGAACCTAAGT[G/T]TTCAAGGTCATGGAG | 10533 |
| rs201177910 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397441 | TATATAAAAAATTTA[A/C]AAGAACTACCAGAAA | 10533 |
| rs201181191 | in-del | -/AAAAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339310 | CAAAAAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAC | 10533 |
| rs201210520 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11502045 | ACACACATACACACA[C/T]ATGTTTATATATATG | 10533 |
| rs201211334 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338499 | CACAGAAAAACAATT[C/T]TGAAGTCTTAACCTC | 10533 |
| rs201212802 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451801 | AAAAAAAAAAAAAAC[A/C]AATTAAAAAAACCCC | 10533 |
| rs201234890 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413601 | GACTTAATAAATGAA[A/T]TCAGCAAAGTAGCAG | 10533 |
| rs201237102 | snp | A/C | 4.94181e-05 | 0.00497057 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11298758 | CCCTTTTAGTAGTGC[A/C]TTGGATGTTGGGTTT | 10533 |
| rs201237561 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466882 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 10533 |
| rs201244311 | in-del | -/A | 0.0329836 | 0.124112 | intron-variant | ATG7 | GRCh38.p7 | 3:11464362 | GGGTGAACGAGCAAG[-/A]ACCCTGTCTCAAAAT | 10533 |
| rs201258273 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306988 | AGCTATTGGAACACT[A/G]TATAACACCAACACA | 10533 |
| rs201258924 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389258 | AAAAAAAAAAAAAAA[C/T]ATGTGAAAGAACTGT | 10533 |
| rs201276770 | in-del | -/ACAA/ACACAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478993 | GTATATTTACAACAC[-/ACAA/ACACAA]ACACACACACACACA | 10533 |
| rs201284090 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11521102 | AAAAATGCCTGTCTC[A/G]CAGCAATGCTGAGAC | 10533 |
| rs201290660 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11497135 | CAGGAGTGAGCCCCC[-/C]ACGCCCAGCCCCTAA | 10533 |
| rs201325339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490295 | ACTAGGATTGCAACC[C/T]CTGCCTTTTTTTGTT | 10533 |
| rs201330012 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322228 | ACACATACACATAAC[A/C]AAACAAGACTTTTGC | 10533 |
| rs201337816 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11431151 | CACGCCTGTAATCCC[A/C]GCACTTTTGGGAGGC | 10533 |
| rs201349662 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11305768 | TTTGAGCCTGACAGA[C/T]GGCATTTGACAGAGC | 10533 |
| rs201358717 | in-del | -/CT | 0.0614824 | 0.164198 | intron-variant | ATG7 | GRCh38.p7 | 3:11306118 | TGCTTACTCTGAGGA[-/CT]CTGTGAGGCCTTTGG | 10533 |
| rs201365166 | in-del | -/TGTTT | 0.0310518 | 0.120672 | intron-variant | ATG7 | GRCh38.p7 | 3:11378721 | AAATTGCTGTAGGCA[-/TGTTT]TGTTTTTCCAGGTTT | 10533 |
| rs201382020 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11554249 | GTCTCCACTGTCTTT[-/G]CTCCAGGCCACCTCC | 10533 |
| rs201383028 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299337 | TCTGACTTGTCATTG[A/C]AAATGTGATAATGCT | 10533 |
| rs201384830 | snp | A/G | 3.31669e-05 | 0.00407215 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313411 | GGATCAAAGGTTTTC[A/G]CTAAAACAGGTATCA | 10533 |
| rs201404576 | in-del | -/AGA | 0.0551013 | 0.156571 | intron-variant | ATG7 | GRCh38.p7 | 3:11341386 | ACCTTGAAGGATATT[-/AGA]AGAATTATTTCATGG | 10533 |
| rs201411636 | snp | C/T | 0.00305976 | 0.0389938 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11364686 | TGCCAGCAGCAGTGA[C/T]GATCGGATGAATGAG | 10533 |
| rs201411851 | in-del | -/AG/CA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400840 | TTACAAACGTCACTC[-/AG/CA]AGGGTAATAATTTTC | 10533 |
| rs201437105 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441369 | ACCTCAACCTCCCGA[-/AT]AGCTGGGATTACAGG | 10533 |
| rs201456493 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440517 | TTTTAGTAGAGACGG[-/G]GTTTCACCGTTTTAG | 10533 |
| rs201459450 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517340 | GCCAGACTCCACCTC[-/A]AAAAAAAAAAAGAAA | 10533 |
| rs201461612 | in-del | -/TAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11375039 | AGACCTCATCTCTCT[-/TAA]AAAAAAAAAAAAAAA | 10533 |
| rs201462812 | snp | C/T | 0.399968 | 0.200024 | intron-variant | ATG7 | GRCh38.p7 | 3:11489955 | aaatgtatattctat[C/T]gatttggggtggaga | 10533 |
| rs201491705 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11507963 | TAATTAAAAAAAAAA[A/C]AAAAAAACAAAAAAC | 10533 |
| rs201497105 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331456 | GTGTGTGTTTGTCTG[C/T]CTGTCTGCCTTTGCC | 10533 |
| rs201517761 | in-del | -/AAAAG | 0.322007 | 0.239405 | intron-variant | ATG7 | GRCh38.p7 | 3:11517348 | CCACCTCAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 10533 |
| rs201548214 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490579 | CCTCCATGGTCTTTA[A/C]AATTTGGCATGATTT | 10533 |
| rs201556959 | snp | A/G | 0.303938 | 0.244112 | intron-variant | ATG7 | GRCh38.p7 | 3:11517352 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 10533 |
| rs201563825 | snp | C/T | 0.000115797 | 0.00760823 | intron-variant | ATG7 | GRCh38.p7 | 3:11306923 | CTGTGCCTGACTAAC[C/T]GTGTTTCTCTTGTAT | 10533 |
| rs201567359 | snp | A/T | 0.198014 | 0.244535 | intron-variant | ATG7 | GRCh38.p7 | 3:11501549 | GATAATGATATTAAT[A/T]GATAGGTGTGATAAT | 10533 |
| rs201580060 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438600 | TAAAGATTTTTTTTC[C/T]TTTTAACCTAAATTC | 10533 |
| rs201593982 | snp | A/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286912 | ACCCAACCTTTTTTT[A/T]TTATTATTATTATTT | 10533 |
| rs201617539 | snp | C/G | 0.499846 | 0.00878459 | intron-variant | ATG7 | GRCh38.p7 | 3:11485897 | TTCTGTTCCATTGAT[C/G]TATATCTCTGTTTTG | 10533 |
| rs201624243 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424608 | ATTTTAATAAATATT[A/T]ATTTTTAATATTAAA | 10533 |
| rs201637675 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487592 | GGCCGGGCGGGGGGC[C/T]GACCCCCCCACCTCC | 10533 |
| rs201645133 | in-del | -/ACAT | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11502043 | TACACACATACACAC[-/ACAT]ATATGTTTATATATA | 10533 |
| rs201686903 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279726 | TAAAAAGCAAACAAA[-/C]AAAAAAACCCCACCT | 10533 |
| rs201698632 | in-del | -/GCTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520435 | AAGAGCTATAATTCT[-/GCTTA]TAGCTCAGCAGCGAG | 10533 |
| rs201706487 | snp | A/C/T | 0.000351314 | 0.0132489 | synonymous-codon, stop-gained, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426822 | CTTGATCAATATGAA[A/C/T]GAGAAGGATTTAACT | 10533 |
| rs201708045 | in-del | -/T | 0.375399 | 0.216275 | intron-variant | ATG7 | GRCh38.p7 | 3:11389438 | AAGTTTTGTTAGTGC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs201709024 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417805 | TATTATTATTATTTT[A/T]TTTTATTTTATTTTT | 10533 |
| rs201720396 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11492047 | TTGGCAATGGTGGGC[A/G]CCCCTCCCCCAGCCT | 10533 |
| rs201722525 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11485340 | TGCATAAATGTCGTC[-/T]TTTGAGAAGTGTCTG | 10533 |
| rs201722846 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349238 | CTAGACAGAAAAGTT[-/C]TCCCAAGTCCCCACT | 10533 |
| rs201732587 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | ATG7 | GRCh38.p7 | 3:11501447 | TTTTGAGTGGTACAG[-/A]AAAAATCTACAGTGT | 10533 |
| rs201740704 | in-del | -/A/CTTA | 0.158302 | 0.232576 | intron-variant | ATG7 | GRCh38.p7 | 3:11489491 | TCCTTCAGTTCTGCT[-/A/CTTA]CTTTAGTTATTTCTT | 10533 |
| rs201753455 | in-del | -/GC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372850 | TGCGTGCGTGCGTGT[-/GC]GTGTGTGTGTGTGAA | 10533 |
| rs201766418 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499260 | TTGCCACATTCCTCT[A/T]TCCTTTCCTGTTCTA | 10533 |
| rs201772380 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11398096 | TCCAAAAAAAAAAAA[-/A]GGAAAATTTTAATGA | 10533 |
| rs201778752 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11384767 | AGAGTTTGAGACCAG[-/C]CTGGGTAACATGGTG | 10533 |
| rs201783956 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11367141 | TAGGCTTTAAACAAC[-/T]TTTTTCCCCCTAAGT | 10533 |
| rs201786096 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400840 | ATTACAAACGTCACT[C/T]AGGGTAATAATTTTC | 10533 |
| rs201807892 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11328288 | ATTAAACTGTGGCTT[A/C]GAGGGTTGAGTACTT | 10533 |
| rs201810263 | in-del | -/T | 0.0448719 | 0.142907 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556614 | AAAAAAAAGATCAAC[-/T]TTTTTTTTTCCGAAC | 10533 |
| rs201823363 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515295 | TCACTGTGTCTCTTG[C/T]GCGTGTGTGTGTATG | 10533 |
| rs201827446 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508351 | AAAAAAAAAAAAAAA[A/G]AAAAAATTCATACTG | 10533 |
| rs201829835 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332194 | TGATGAAATGTCATA[A/T]ACAATGAATCTGAGT | 10533 |
| rs201834030 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11428398 | TGAGCAGATTGTGAG[-/A]TTTTTCAGGTACACC | 10533 |
| rs201843881 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385272 | TGACCTTGTAATCTG[C/T]CCACCTCGACCTCCC | 10533 |
| rs201850579 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349240 | AGACAGAAAAGTTCT[C/T]CCAAGTCCCCACTCA | 10533 |
| rs201851690 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338464 | TCAATTAATGGCAGG[G/T]GGGAACTCTTTTTTT | 10533 |
| rs201858456 | snp | A/C | 0.151668 | 0.229849 | intron-variant | ATG7 | GRCh38.p7 | 3:11337486 | TCTCTCTCTCTCTCT[A/C]TCTATATATATATAT | 10533 |
| rs201868294 | in-del | -/C | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11334879 | GAAGAATCGCTTGAA[-/C]CTGGGAGGTGGAGGT | 10533 |
| rs201875988 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415774 | TTTTTTTTTTTTTTT[-/T]AAATAAGTAGAGGGA | 10533 |
| rs201884008 | snp | C/T | 0.000296526 | 0.0121727 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347952 | GTGAGGCAGCCTCTC[C/T]ATGAGTTTGAAGATT | 10533 |
| rs201893252 | snp | A/G | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527077 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 10533 |
| rs201908594 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11358019 | TCTCAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG | 10533 |
| rs201908905 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502033 | GTAAACATATATACA[C/T]ACATACACACATATG | 10533 |
| rs201957165 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382918 | ATTTGCTGTCGTCCT[C/G]CAATCCCTCCTTCTT | 10533 |
| rs201963236 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294031 | CAAAAAAAAAAAAAA[-/G]AAAGAAAAAGAAAGA | 10533 |
| rs201989333 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | ATG7 | GRCh38.p7 | 3:11383874 | ATTTGTGCATAGTTC[-/T]TTTTTTCCTAGGTAA | 10533 |
| rs201999050 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ATG7 | GRCh38.p7 | 3:11511777 | AGCGAGAAATCGAGC[A/G]CAGCACCGGTGGGCT | 10533 |
| rs202001978 | snp | A/G | 0.000280105 | 0.0118311 | intron-variant | ATG7 | GRCh38.p7 | 3:11331441 | ATGGTATTTACAAGA[A/G]TGTGTGTTTGTCTGT | 10533 |
| rs202012963 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487393 | GCAGAGGGGCTCCTC[A/G]CTTCCCAGTAGGGGC | 10533 |
| rs202020977 | snp | A/C | 0.0003957 | 0.0140604 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306951 | TATCTAGGAGTGCTC[A/C]CACCCCAGCCCGTTG | 10533 |
| rs202025031 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462031 | TGAGACTCTGTCTCC[-/A]AAAAAAAAAGAAAGA | 10533 |
| rs202028672 | snp | A/G | 0.00199805 | 0.0315442 | intron-variant | ATG7 | GRCh38.p7 | 3:11315306 | CAGAACTAGAAATGT[A/G]ATTTTCTAGAGAATA | 10533 |
| rs202032193 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491488 | GTCAAAGTCATTCTC[C/T]GTCCAGCTTTGTTCC | 10533 |
| rs202038106 | snp | A/T | 0.00199792 | 0.0315431 | intron-variant | ATG7 | GRCh38.p7 | 3:11426948 | ACAAAACAAGCTTTC[A/T]GTAGTGAAGACTGAC | 10533 |
| rs202058873 | snp | A/C/G/T | 5.39994e-05 | 0.00519589 | intron-variant | ATG7 | GRCh38.p7 | 3:11426791 | CTTTTTAAAAAATGT[A/C/G/T]AATGTTTTACAGGTT | 10533 |
| rs202071299 | in-del | -/GATT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537997 | TGAATGTAGAAGAGG[-/GATT]CCAGGGAAAGGTGGA | 10533 |
| rs202080204 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441671 | TTTTTTTTTTTTTAA[A/T]TTTTTTTTTTTTTGA | 10533 |
| rs202087285 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298179 | GACTCCATCTCAATT[-/A]AAAAAAAAAAAAATC | 10533 |
| rs202088956 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337486 | CTCTCTCTCTCTCTC[-/TA]TCTATATATATATAT | 10533 |
| rs202092188 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326297 | TGCTGTTTTTTTTTT[G/T]TTGTTGTTGTTTTGT | 10533 |
| rs202097573 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345671 | TTGCTAGAGAGGCTT[A/C]TCTATCAGTTTTTTT | 10533 |
| rs202098105 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397442 | ATATAAAAAATTTAC[A/C]AGAACTACCAGAAAT | 10533 |
| rs202101306 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462847 | CTCAGATATTTTTAT[A/T]TATTTATTTATTTAT | 10533 |
| rs202109061 | snp | A/G | 5.19638e-05 | 0.00509698 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554879 | GACTTCTCCCCGGCC[A/G]CCTGCTGAGGAGCTC | 10533 |
| rs202110005 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474091 | TACCAAGTGTGTAGT[A/T]AGCCAAGTGCCACCA | 10533 |
| rs202117370 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11275389 | AGTCTCACTCTGTCG[C/T]CCAGGCTGGAGTGCA | 10533 |
| rs202139677 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480842 | GGCAAGTAGCCTCCA[G/T]TCCTGGCCGGCTGGG | 10533 |
| rs202141570 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11465643 | GTGGCACACACCTGT[-/A]AGTCCTAGCTACTTG | 10533 |
| rs202152692 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | ATG7 | GRCh38.p7 | 3:11486822 | TGTCTTTGGTTCTGT[G/T]TTTTTTTTTTTTTTT | 10533 |
| rs202166590 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372805 | GGTAAGGGCTGGGTG[G/T]GTGTGTGTGTGCGCG | 10533 |
| rs202173656 | in-del | -/TAAAA | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11478820 | AGCCCAAACTTGAAT[-/TAAAA]TAAAGTTATTCTCAA | 10533 |
| rs202174179 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424985 | TATCCCTTTTTTTTG[G/T]TTTTGAAGACTCTGT | 10533 |
| rs202174843 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372837 | GTGTGCGTGTGTGTG[C/T]GTGCGTGCGTGTGCG | 10533 |
| rs202189529 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489142 | CTTGGGAGGGTGTAT[A/G]TGTCGAGGAATTTAT | 10533 |
| rs202195387 | in-del | -/C | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11552947 | TCCTATAAAGCCCAG[-/C]CCCCGGCCCAGGCCC | 10533 |
| rs202200903 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465753 | TGGGCGACAGCGAGA[-/C]CCCTGCTTCAAAAAA | 10533 |
| rs202208342 | in-del | -/GA/GAG/GAGCCA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397738 | TGGGATTACAGGCGT[-/GA/GAG/GAGCCA]GCACCCACGCCCAGC | 10533 |
| rs202217827 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294397 | GGCTAATTTTTTTTT[A/T]TTTTTAGTAGAGATG | 10533 |
| rs202224623 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470010 | AAAAAAAAAAAAAAA[C/T]AGAGAGAGAGATGGT | 10533 |
| rs202247728 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456673 | TTTCTTTCTACTCCC[C/T]CCACTACCGACCACT | 10533 |
| rs207462996 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353234 | GGATCACGAGGTCAA[C/G]AGATCGAGACCATCC | 10533 |
| rs367546941 | in-del | -/GT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372828 | TGTGCGCGCGTGTGC[-/GT]GTGTGTGCGTGCGTG | 10533 |
| rs367548558 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11501784 | AGCCTTCGCCTCCCG[A/C/G]GTTCAAGTGATTCTC | 10533 |
| rs367561267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510902 | TGGTGGGTTCTTGGT[C/T]TCACTGACTTCAAGA | 10533 |
| rs367575200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493314 | AGTCGCCTCTCCCCA[A/G]CATCCAGCTGCTTCT | 10533 |
| rs367581898 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516066 | AAAACATAGGACATA[G/T]TTCCTAAGCTGATGT | 10533 |
| rs367585913 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542847 | AAGTGTAGCTCGGAG[A/G]TGCTGACCTTCCTCT | 10533 |
| rs367586886 | in-del | -/CT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351011 | CCCAGACAGACCTGG[-/CT]CTTTGAACCTGAGCT | 10533 |
| rs367635177 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550307 | TGCATCTTTTTTTTT[-/T]CTGTTTAAGGGCCAT | 10533 |
| rs367661117 | snp | C/T | 0.00013781 | 0.00829975 | intron-variant | ATG7 | GRCh38.p7 | 3:11342329 | TGAAGTTGTAGCTTC[C/T]CTTCTTGTTTTACTC | 10533 |
| rs367705750 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303487 | ATCCTGGCTAACATG[A/G]TGAAACCCCGTCTCT | 10533 |
| rs367748854 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11446283 | CTATATCCATTTCAA[C/G]ATTCTGTGATAACGA | 10533 |
| rs367775941 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11361575 | GGTGTGAGCCACCAC[A/G]CTTAGCCAATAATGA | 10533 |
| rs367789122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431344 | AGGTGGAGGCTGCAG[C/T]GAGCTGAGATTGTGC | 10533 |
| rs367818553 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309559 | TCGTATTAGGGTAAC[-/AT]GTGCTGCCCAGTGAA | 10533 |
| rs367820861 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11362266 | AGAGCCATGTTGTAG[-/A]AAAAAAAAAATACTT | 10533 |
| rs367835299 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353226 | AGGCGGGTGGATCAC[A/G]AGGTCAAGAGATCGA | 10533 |
| rs367836832 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11374676 | TTTGGGAGTCCGAGG[A/C/T]GGGCAGATCGTGAGG | 10533 |
| rs367838876 | in-del | -/TC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286582 | TTTTCTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTT | 10533 |
| rs367851882 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ATG7 | GRCh38.p7 | 3:11360804 | GTGGATTTCTCTATA[C/G]TTCCAAATATTTCCT | 10533 |
| rs367853949 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295772 | CTATTTCTTTCTTTC[-/T]TTTCTTTCTTTCTTT | 10533 |
| rs367897739 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395878 | CGAGGAGGCGGAGCT[C/T]GCAGTGAGCGGAGGT | 10533 |
| rs367900538 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395644 | CCAGCAGATAATACC[A/G]TTCAAGAATGAAAGG | 10533 |
| rs367914394 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295237 | TTTAGGGACAGTGAT[A/G]TGTTGTCTTTTGTGA | 10533 |
| rs367915123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371351 | CCAGTTTACCTGCGA[A/G]ACAGCGAGTAAAGGG | 10533 |
| rs367919727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352597 | AGTTTCTTCATTCAA[C/T]AGATACTTATTCATC | 10533 |
| rs367928825 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344503 | CATTCCTAGAATAAA[C/T]CCTATTTGTACGTGG | 10533 |
| rs367937207 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11303720 | AAATGATCAACATTT[A/G]AATGAAGAACATTTC | 10533 |
| rs367939647 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507700 | ATTCTATTCATGGAC[C/T]CCTTGAGGGTCTGAG | 10533 |
| rs367945392 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308187 | CTGCTTACTTATTTC[C/T]CTCTTCCACCCACAC | 10533 |
| rs367946566 | in-del | -/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11527895 | TTTCATTTCCTTGTT[-/TG]TGACTACAAACACAG | 10533 |
| rs367976942 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11437666 | ACTCCTACCTGGATC[C/T]AACAATTAACATTTT | 10533 |
| rs367979777 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334578 | TGTTCCTTATATCAT[A/C]CTCATGGTTCCAAGG | 10533 |
| rs367986710 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542036 | ACAAGCCTGGGGCCC[A/G]TGCCCTCCTCCCACA | 10533 |
| rs367993055 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317584 | GCCCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs367993422 | in-del | -/CAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484413 | GAAAAAACAAACAAA[-/CAAA]AAAACCACAAAAACG | 10533 |
| rs368014315 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445484 | GGAGCTGAATCATGA[A/G]AACACATGGACACAT | 10533 |
| rs368015932 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11370473 | ATTAAGACTCTTTTC[A/G]GCATCCAAGATCGAT | 10533 |
| rs368025891 | in-del | -/GTGCTGTGGCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524209 | TCCCCTTCACTAGCT[-/GTGCTGTGGCT]TAGTTAAGCTGAAGT | 10533 |
| rs368030037 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11331923 | ATTTAATAAAAATGT[C/G]TGTACCAAGTGTTGT | 10533 |
| rs368070269 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470876 | TATTACTTTCTTGCC[A/G]TATTACTCTCGTTCA | 10533 |
| rs368096877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11378416 | GGCTGGGCGCGGTGG[C/T]TCACGCCCGTAACCC | 10533 |
| rs368104489 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487116 | TTTAACCCTGAGTGG[A/G]CACAGCACATGTTTC | 10533 |
| rs368116912 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440343 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 10533 |
| rs368117599 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523714 | ATGTCGGCCCTGGAA[A/G]CAAAACTGTACCTTG | 10533 |
| rs368161814 | snp | A/C | 1.64838e-05 | 0.00287083 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298858 | TATTACTACAATGGT[A/C]GGTGATTGTAAATTT | 10533 |
| rs368178322 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462268 | GCTAAGGGCTGTTTT[A/G]TGTTCTTTTATGAGA | 10533 |
| rs368179260 | snp | A/G | 0.000152113 | 0.00871971 | intron-variant | ATG7 | GRCh38.p7 | 3:11333121 | TCTTTGAAAATGCAT[A/G]TAATTATCATTTATC | 10533 |
| rs368187179 | snp | A/G/T | 0.000798343 | 0.0199636 | intron-variant | ATG7 | GRCh38.p7 | 3:11554766 | TGTGTGCCCCCCACC[A/G/T]GGCAGTGGGACATCT | 10533 |
| rs368187544 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439061 | TTTTCTTTTTCTTTT[C/T]TTTCTTTCTTTTTTT | 10533 |
| rs368191937 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490500 | TTGTTATGTGTGAAT[C/T]TGATCCTGTCATTAT | 10533 |
| rs368208971 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11554712 | AGGGAGTGGTTCTGC[A/G]GGTGGGAGCTGCCAT | 10533 |
| rs368255357 | snp | C/T | 8.32522e-05 | 0.00645129 | intron-variant | ATG7 | GRCh38.p7 | 3:11554765 | CTGTGTGCCCCCCAC[C/T]GGGCAGTGGGACATC | 10533 |
| rs368257549 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529973 | GGGCCCAGAGACTTC[C/T]TTCTCACTCCTTTTC | 10533 |
| rs368258357 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378685 | GTGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs368279429 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294199 | AGAGTGTTTCTACAC[A/G]TGTGCCTCAAATCCT | 10533 |
| rs368298408 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542303 | GACATCCCCAGAGGG[A/C]GGGTGCCAAATATAG | 10533 |
| rs368317547 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11283674 | GGACATGGTGGCTCA[C/T]GCCTAGTAATCCTAG | 10533 |
| rs368331681 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11414711 | GAGATTTTGTGGATG[G/T]TCTTTATCAAGTTGA | 10533 |
| rs368380541 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11544440 | GCCTGGGGCCTCTTA[-/A]GAGTCCAGAAGCAAG | 10533 |
| rs368385096 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11443881 | ATATAGAGAACAAGT[A/G]TGAATTAAACACCCA | 10533 |
| rs368405710 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331206 | TTCTTCTCCTCCCCT[G/T]AGCCCTTTACCAGAT | 10533 |
| rs368414798 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369737 | AGCGTTCAGAAGCAT[C/T]TCAGATTGCATCTCT | 10533 |
| rs368416147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348496 | CTCTTAAAGATGATG[A/T]GTCTGGAGTTTGTTC | 10533 |
| rs368428666 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11327938 | CATGCTGCTGGGGCA[C/T]GGACCACATTTTGAG | 10533 |
| rs368442797 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499262 | GCCACATTCCTCTAT[C/T]CTTTCCTGTTCTACA | 10533 |
| rs368448168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323769 | TCTTTCTTCACTTAG[C/T]GATCTCTCCGCATCT | 10533 |
| rs368449197 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378926 | TAAACGGTGGTGGAT[C/T]GGGTCTTCTGTTCTG | 10533 |
| rs368467179 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390861 | TGAGCTAAGAGCTGG[A/C]AGGACATTTTGATAT | 10533 |
| rs368484931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398681 | AACATAGCAAGACCC[C/T]GTCTCTACAGAAAAT | 10533 |
| rs368486272 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280223 | GGCCCTTTTTTTGTA[C/T]TTTTAGTAGAGACGG | 10533 |
| rs368496576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443179 | CACTTCTGTGTGGGG[C/T]GTGCTCCCACCTCCA | 10533 |
| rs368506515 | in-del | -/AAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378686 | TGAGACTCCATCTCC[-/AAA]AAAAAAAAAAAAAAA | 10533 |
| rs368545804 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11375895 | CTTTGGAAAACAAGT[A/T]GGCAGTTCCTCAAAA | 10533 |
| rs368565652 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485709 | AATCCATCTTGAATT[A/G]ATTTTTGTATAAGGT | 10533 |
| rs368566141 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11511818 | GGGTACTCAGTACAC[C/T]CTCCGCAGCCACTGG | 10533 |
| rs368581555 | snp | A/G | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451634 | GGCTGTTGTGTCCAT[A/G]AGAGAACTCCTGGGA | 10533 |
| rs368582077 | in-del | -/G | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11493191 | GAGGGGAGCTGGAAA[-/G]GGGGTGGGAAGGCCA | 10533 |
| rs368583309 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453826 | CAAGGGGTGGGGGGG[-/G]ACATCTGGAGCCTGA | 10533 |
| rs368584886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11466662 | TCTTACTGCTCTTTT[C/T]GGAAAAAGCAGTTCT | 10533 |
| rs368585077 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415315 | GAGTGACTGTGAAGG[C/T]CTAGGACATTTTGTA | 10533 |
| rs368588298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509867 | AAATCAGGCAGCCAG[C/T]GCTCCATACTTATTT | 10533 |
| rs368588440 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439656 | ACGTGGTGCAGTAAG[A/T]TCTGCAGGGTTTCAG | 10533 |
| rs368598930 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417811 | TATTATTTTATTTTA[-/TT]TTATTTTTTTTTTTT | 10533 |
| rs368619706 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439045 | TGAGCTCTTAGTCTT[A/T]TTTTCTTTTTCTTTT | 10533 |
| rs368623073 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539178 | GTGTACCCTGCATCA[A/G]GTGCAGTTCTGAGCA | 10533 |
| rs368628351 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487352 | ATGAGCTGTTGGGCA[C/T]ACCTCCCAGACGGGG | 10533 |
| rs368633027 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495089 | CTCAGAAAAAAAAAA[-/A]GGCTTGAACAGATGT | 10533 |
| rs368633116 | in-del | -/GT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465089 | CTCTAAAAACCTAAA[-/GT]GTGTGTGTGTGTGTG | 10533 |
| rs368633120 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513161 | CAAGTCCCCACCAGA[C/T]TCAGGAGCCCAGCTG | 10533 |
| rs368656211 | snp | A/G/T | 6.70209e-05 | 0.0057885 | intron-variant | ATG7 | GRCh38.p7 | 3:11362949 | TTTGCTAGTAGGAGA[A/G/T]GAGTATTTAAACAAA | 10533 |
| rs368667518 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452384 | GCGAGAACCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs368671156 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ATG7 | GRCh38.p7 | 3:11307067 | GCAAATGAGGTTAGC[G/T]GTGAAAACGTGATGT | 10533 |
| rs368675792 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340007 | CTTTGGGAACTGCTA[C/G]AATTGGAGTTAATTG | 10533 |
| rs368679108 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379868 | ATCTCTTTCCGGGCC[A/G]CCATATTAATCATTT | 10533 |
| rs368682840 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11343445 | TATTCATGTTCTTTG[A/G]GTTGTGTCTTTTATT | 10533 |
| rs368692885 | snp | G/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271241 | TTTTTTTTTTTTTGA[G/T]ACGGAGTCTCGCTCT | 10533 |
| rs368693759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278328 | ACAATTTATGTTCAG[A/G]GATTGAAGTAAAGAC | 10533 |
| rs368698099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11518013 | AGAAAGAAGTAGACA[A/G]TTGAATCGATGTTGA | 10533 |
| rs368707744 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404378 | TGACTTCAAGTGATC[-/T]GCCCTGGTTGGCCTC | 10533 |
| rs368733239 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11536729 | ACCGGGGCCGAGCAG[C/T]GAAGGACCACCCTGG | 10533 |
| rs368764138 | snp | C/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273920 | GGAAGTGACCTAACA[C/G/T]TTGAATAAAGAAAAG | 10533 |
| rs368773431 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508394 | TTACAAATTTGTGTT[A/G]GGCTGCATTCAAAGC | 10533 |
| rs368786254 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294398 | GCTAATTTTTTTTTA[A/T]TTTTAGTAGAGATGG | 10533 |
| rs368791572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11426241 | TTTGATAGGTGCAAA[A/G]TAGTGTTTCATTGTG | 10533 |
| rs368802513 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533556 | AAAAAAAAAAAAAAA[-/A]GCCATTACACAAATA | 10533 |
| rs368805633 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11383059 | TTACCTAAACACAAT[A/G]TCCTTATCAAATTCA | 10533 |
| rs368825270 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11449587 | AGAGAATGATTTTCC[C/T]GACCCTTCCCTTGGG | 10533 |
| rs368831499 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485971 | AGTTTGAAGTCAGGT[A/G]GCGTGATGCCTCCAG | 10533 |
| rs368832246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11554361 | AGGGAACATGGAGCA[C/G]GTGCCCAGGGTGCAG | 10533 |
| rs368833660 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499483 | AGGCGCAGTGGCTCA[C/T]GCCTGCAATCCCAGC | 10533 |
| rs368836880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11533478 | CATGTTGTTCACAAC[A/G]TGAACTTTGATTTGT | 10533 |
| rs368837128 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550366 | GTCTTTGTCCACTTT[C/T]TAAAAATTTGGTCTA | 10533 |
| rs368838450 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11375565 | AGTGAGATTTTTTTT[C/T]CCCCTTGCCCCCAAG | 10533 |
| rs368844304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11456525 | ATTGCTGTATTGTGT[C/T]GTAACTTTTTTGTTC | 10533 |
| rs368846094 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440575 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10533 |
| rs368849264 | in-del | -/CCAGGGAAAGGTGGAGGGAAGAGGGCATAGGTCCCAGTGTGG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537998 | TGAATGTAGAAGAGG[lengthTooLong]GATTCCAGATGACCC | 10533 |
| rs368889423 | in-del | -/GAGGGCTGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513787 | GGCTGCGAGGGCTGC[-/GAGGGCTGC]CAGCATGCTGTCACC | 10533 |
| rs368901520 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503895 | AAAGACAAAGAAATG[A/G]AAAATAAGGGAGAAA | 10533 |
| rs368920284 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502471 | TGAGTGAGAATATGC[A/G]GTGTTTGGTTTTTTG | 10533 |
| rs368984185 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11460092 | TAAAGCAATAATAAC[C/T]AGTTTAAATGTAGGC | 10533 |
| rs369009750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11540887 | TTTTTTCCTAAAAAA[C/T]TTATAGTTTTAGCTT | 10533 |
| rs369034852 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489883 | ACATTTGCTGAGGAG[A/T]GCTTTACTTCCAAGT | 10533 |
| rs369041185 | snp | A/C | 1.66023e-05 | 0.00288113 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315399 | CAGAAGGAGTCACAG[A/C]TCTTCCTTACTTCTT | 10533 |
| rs369095431 | in-del | -/A | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11510383 | TCCCTGCCCCAGTTT[-/A]AAAAAAAAAAAAAAT | 10533 |
| rs369105181 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11364327 | GGCCTCTGATATGCC[A/G]AACATTGCACTCGGC | 10533 |
| rs369114629 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ATG7 | GRCh38.p7 | 3:11380095 | GTTTTTAAAAGTGAG[C/T]GGGTCAGCATTTGAC | 10533 |
| rs369115899 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366052 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 10533 |
| rs369122417 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11328226 | TATCAGCTCATTTAA[C/T]CCTCACTACAGCTCT | 10533 |
| rs369153407 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11291151 | ACAAGTTACATTTGT[A/C]CTTGAAGAGAAAGTT | 10533 |
| rs369155509 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392480 | AACAAACAAAAAAAA[-/C]AAAACAAAACAAAAA | 10533 |
| rs369155891 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489431 | CTTTCAAAAAAACCA[A/G]CTCCTGGATTCATTA | 10533 |
| rs369164996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11479626 | AAAAGGAAAGGAAAA[A/G]CTATTGGATAGCAAT | 10533 |
| rs369182128 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458904 | GATCAGCGGAGCATT[A/G]GATTCTCATAGGGGC | 10533 |
| rs369182231 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11536612 | GTTTTCAGAGTAAAC[A/G]TTTGTGTGAGCGCAC | 10533 |
| rs369208276 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372673 | GACCATTTTTATTTT[C/T]TCTGTATATTTTACT | 10533 |
| rs369214414 | in-del | -/AACA/AACACACA/AACC/AC | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11478998 | TTTACAACACACACA[-/AACA/AACACACA/AACC/AC]CACACACACACACAC | 10533 |
| rs369231815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416268 | CTTCTGAAAGAGATT[G/T]TAGATGATTGGTATA | 10533 |
| rs369243858 | in-del | -/AACAT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389320 | ATGACTTGTTCATAT[-/AACAT]GTTATACTGTATTTA | 10533 |
| rs369245076 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411588 | TCACGCCACTGCACT[C/G]CAGCCTGGTGACACA | 10533 |
| rs369267375 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279609 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 10533 |
| rs369288647 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488014 | TCCCAGATGGGGCGG[C/T]GGGGCAGAGGTGCTC | 10533 |
| rs369291139 | snp | C/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450683 | ATTTCCAGAGAGTTG[C/G]AGGGATATTAAATTT | 10533 |
| rs369295714 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473018 | TTTGTAACTAATCAA[C/T]GATTTCTGACATTCA | 10533 |
| rs369308907 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315922 | AGTAGAGACAGAGAC[A/G]AGGTTTCACTATGTT | 10533 |
| rs369320614 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532534 | TAGAGACCAGCCTGG[A/G]CAACATGGCAACGTC | 10533 |
| rs369332323 | snp | A/C | 6.61496e-05 | 0.00575069 | intron-variant | ATG7 | GRCh38.p7 | 3:11331295 | GTCTGTATTGTGAAG[A/C]TGACATGATACTCGA | 10533 |
| rs369334309 | in-del | -/TC | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288487 | GCTGCTAGTCTTTTA[-/TC]TCTCTCTTTGTCTTC | 10533 |
| rs369351882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351561 | TGCTGGGCCTGAGAG[A/G]GCAAGTCCAACTGTT | 10533 |
| rs369352712 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11471791 | ATCGCCCAGGCTGGA[A/G]TGCAGTGGTACAGTC | 10533 |
| rs369365717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11521807 | TCCGCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 10533 |
| rs369377974 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ATG7 | GRCh38.p7 | 3:11490549 | TGCTCGTTAGTTGAT[A/G]CAGTTTCTTCCTAGC | 10533 |
| rs369389382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505258 | ACGAGTAGGAGTTCT[A/G]TAGGCCTAGGGAATG | 10533 |
| rs369390629 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11427894 | GTGTATGGTGGTAGA[C/G]CTATTTGGATCACTT | 10533 |
| rs369400520 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404530 | CATTCTTAAGGTCAG[C/G]TAGACTGAGTTTAGG | 10533 |
| rs369408734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11368642 | ACAAAAAATTAGCCA[A/G]GTGTGGTGGCACGCA | 10533 |
| rs369413155 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11416642 | ATTTACCTTGTCAAA[C/G]AACTAGCTTTTGGTT | 10533 |
| rs369417745 | in-del | -/AA | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557943 | ATTAAAAAAAACAAA[-/AA]CAGTAACAACAACAA | 10533 |
| rs369427169 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11346213 | TATGCCTTCTGATAG[-/G]ATGAAACATAACTTA | 10533 |
| rs369436921 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411007 | TTTTAATTTTTTTAA[A/G]TAACTGCCATGCTAT | 10533 |
| rs369442149 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556112 | TAAGGCTACTTTTAA[A/G]TACAAAAAAAGATGG | 10533 |
| rs369462716 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499094 | ATAGGTAATTATGTC[C/T]TAACAATTTAGTAGC | 10533 |
| rs369465330 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292448 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10533 |
| rs369465714 | in-del | -/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11321424 | CTCAGTTTTGASYGT[-/TG]GACCAGCATGCAGCT | 10533 |
| rs369474990 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472239 | AACTTTCCATCTCCC[C/T]CTCTTGCCTGGGTTT | 10533 |
| rs369495329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444160 | CTAAAGTTCATTTTC[A/G]TTGCTATGTAGTGTT | 10533 |
| rs369498412 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465088 | TCTCTAAAAACCTAA[A/T]GTGTGTGTGTGTGTG | 10533 |
| rs369514296 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483633 | CTGCCATATTCAAAT[C/T]CTTGTATATAGAAGT | 10533 |
| rs369537467 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11507628 | ATGCTAAAGTTATGG[A/G]TGTTTTTTGTTTTTG | 10533 |
| rs369543605 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528417 | AGATGGTCACGTACC[C/T]CCTATGTGTCAGCCA | 10533 |
| rs369556171 | snp | A/G | 9.88598e-05 | 0.00702995 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299313 | ATTTTTGTTATGAAC[A/G]CTGCTATTTCTGACT | 10533 |
| rs369592282 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311303 | GACCTGATAAAGTTT[A/C]TTAGAATTCGTGAGG | 10533 |
| rs369603674 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11544201 | GAGTTGCCCCAGGTC[A/C]CCATGCTGCGATGGG | 10533 |
| rs369605091 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358462 | TATGCCTGGGCATCC[A/G]GTGAACTTCTCCAGT | 10533 |
| rs369605784 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395965 | AAAAAAAAAAAAAAA[A/G]GGTAGGGGGGGAAGA | 10533 |
| rs369613167 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11511728 | GTGGGCTGCAGGTCC[C/T]GAGCCCTGCCCCGAG | 10533 |
| rs369615779 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423216 | GGCCAGTTGGTGAAT[C/T]GGTCAGAACACATAC | 10533 |
| rs369620338 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278771 | ACATGGTTCCTTTCT[C/T]ATAGAATTTTTATTC | 10533 |
| rs369631739 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464050 | AGTGACAAGAGCAGG[C/T]TGAAAAACAACAGGT | 10533 |
| rs369634989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396569 | ATCACTCGAAGTCAG[G/T]AGTTTGAGACCAGCC | 10533 |
| rs369642095 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487748 | GGGGGGCTGACCCCC[A/C]CCCAGCTCCCTCCCG | 10533 |
| rs369652535 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11453820 | GGGAGTGCAAGGGGT[G/T]GGGGGGACATCTGGA | 10533 |
| rs369680058 | in-del | -/TATATAT | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11334547 | CTGAGCCTGGCCTCA[-/TATATAT]TATTTAGCTTGTTCC | 10533 |
| rs369709975 | in-del | -/AAAG | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299044 | TCTTGTTGTGGGGAA[-/AAAG]AAAGAGAGTAGTGAA | 10533 |
| rs369742938 | in-del | -/TTTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417802 | TATTATTATTATTAT[-/TTTA]TTTTATTTTATTTTT | 10533 |
| rs369743661 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11333171 | CTTTCTTTTCATATC[A/G]TCACAATGGCAGAAG | 10533 |
| rs369774428 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381737 | GACTTGGATTTTAAC[A/G]GCTGTGCTATTCCCA | 10533 |
| rs369777200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400339 | TGTTCCCTCTTATGC[C/T]GAGTACCCAGATAAT | 10533 |
| rs369784740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11528266 | CTGTTATTAAATCAG[C/T]AAGGAGCAGCCCCTG | 10533 |
| rs369815891 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472067 | CTTCAAGATTAAACT[C/T]TACAAAATTATTATA | 10533 |
| rs369841348 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484373 | TACTCTAGCCCGGAT[G/T]ACAGGAGACTCCGTC | 10533 |
| rs369842673 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336346 | CCGATGCTGACATTT[A/C]AACTCAGGAACCACA | 10533 |
| rs369878869 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303388 | AAAAAAAGAATTTTC[C/T]GCCAGGCGCGGTGGC | 10533 |
| rs369881536 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508602 | CTGGTGTACCACCAT[A/G]CCTGCTAATATTATT | 10533 |
| rs369888580 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440346 | TTTTTTTTTTTTGAG[A/T]CGGAGTCTCGCTCTG | 10533 |
| rs369912226 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345933 | GAAGACACTCATTTT[C/T]CTACCGCTTTTTCAC | 10533 |
| rs369923041 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480802 | CTGGGAGAGCGAGGA[C/G]GGCCTATCCACTGGG | 10533 |
| rs369925745 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508043 | GCTAGTAGGATAAAC[A/C]ACAGCCTCTACCACA | 10533 |
| rs369940649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11543729 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10533 |
| rs369954525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11511514 | TGTCCCCACCAGACT[C/T]AGGAGCCCAGCTGGC | 10533 |
| rs369964682 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11386037 | TAGGGAGTTTCCTAG[A/C]CTAAGGAATCCAGCA | 10533 |
| rs369991964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11544814 | GAATCATTGTTCCTG[C/T]AAAGCCTCTCTACTA | 10533 |
| rs369991972 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349392 | AAATAAAATTAGCCA[C/G]GTGTGGTGGTGGTGT | 10533 |
| rs370002195 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489953 | AAAAATGTATATTCT[A/G]TTGATTTGGGGTGGA | 10533 |
| rs370006408 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501342 | GATATCAGAAAACCT[A/G]AGAAAAGTGCCTAAT | 10533 |
| rs370010186 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553244 | AGGCCAATTGCCTTA[C/T]CTCTCTGGGCTTGTT | 10533 |
| rs370019515 | snp | G/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271995 | TTGGTCACTGTCGAC[G/T]TTCACTGGCCTTTTC | 10533 |
| rs370026489 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11518352 | AGAGATCGAGACCAG[C/T]TTGGCCAACAATGGT | 10533 |
| rs370026914 | in-del | -/T | 0.395453 | 0.203331 | intron-variant | ATG7 | GRCh38.p7 | 3:11317585 | CCCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs370033434 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469461 | CCTCAAAAAAAAAAA[-/A]GTAAAATAAAATCAT | 10533 |
| rs370047460 | snp | A/G | 0.000100567 | 0.00709036 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554853 | ATCTGAGATGGCCCC[A/G]CTGTGGGGCTGACTT | 10533 |
| rs370071054 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11538641 | GAAGCCCAGGAGTTC[A/G]AGACCACCCTGGTCA | 10533 |
| rs370091619 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540917 | TTTTTGGGGGGGGGA[-/G]GGGGGGGAGTCTTGC | 10533 |
| rs370094457 | snp | A/G | 1.66749e-05 | 0.00288741 | intron-variant | ATG7 | GRCh38.p7 | 3:11313423 | TTCACTAAAACAGGT[A/G]TCAACAAATAACCAA | 10533 |
| rs370114485 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297569 | ACAGTATACGTATGC[A/G]TGATTGCCAGGAAGG | 10533 |
| rs370117541 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11347147 | ATTCATTCCCACCAT[-/T]AACCAGATGTATCTC | 10533 |
| rs370118925 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11521753 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10533 |
| rs370120756 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481885 | AAGGCCTTTGGCCTG[A/G]CAAGAGTTGTCAGGC | 10533 |
| rs370121859 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356279 | GTGCATATGAGATCT[G/T]TGTATTTCACTTTAT | 10533 |
| rs370126792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11430330 | AAATATATGTTAAAA[A/T]ATATATATACCTTTA | 10533 |
| rs370131709 | in-del | -/TGTG | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527042 | GTGTGTGTGTATATA[-/TGTG]TGTGTGTGTGTGTGT | 10533 |
| rs370132168 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378807 | ATCAGGATGGAGTTA[C/T]CCAAAACTCAAAAGA | 10533 |
| rs370138907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11449868 | TAACTGCTGAGAACA[C/T]GTTTTCATTTTGAGT | 10533 |
| rs370146619 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503755 | ACCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 10533 |
| rs370165372 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486420 | TGAAGTTGCTTATCA[A/G]CATAAGGAGATTTTG | 10533 |
| rs370180364 | snp | G/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451517 | AGCACATGAGACAGG[G/T]CACTGGATGGTGTCT | 10533 |
| rs370184345 | snp | A/G | 8.35024e-05 | 0.00646098 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426823 | TTGATCAATATGAAC[A/G]AGAAGGATTTAACTT | 10533 |
| rs370189607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11504500 | AAAGGCATCCTCAAA[A/G]CAGTAGCGAAGGGAA | 10533 |
| rs370201666 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11511888 | CTGGCTGGCTGCTCC[A/G]AATGCGGGGCCCACC | 10533 |
| rs370212428 | snp | C/G | 4.96282e-05 | 0.00498113 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426914 | GCTGCATCAAGAAAC[C/G]CAAGCTGCTGAGGTA | 10533 |
| rs370229562 | in-del | -/GC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372840 | TGCGTGTGTGTGCGT[-/GC]GTGCGTGTGCGTGTG | 10533 |
| rs370233811 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11400223 | ATAACTCATCAACCT[C/T]AGGCTGTAAGAGACT | 10533 |
| rs370243892 | in-del | -/AA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533555 | AAAAAAAAAAAAAAA[-/AA]GCCATTACACAAATA | 10533 |
| rs370257763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347321 | TAAAACCGTGAAAAC[C/T]ATTTCTAAGAATATA | 10533 |
| rs370278762 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ATG7 | GRCh38.p7 | 3:11331475 | TCTGCCTTTGCCAGT[A/G]TATGTTTTACAATGT | 10533 |
| rs370279520 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11360715 | CCTCCTGGGCTCATC[A/G]CTTTTTGCCAACATC | 10533 |
| rs370308890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11514598 | TATGGTGATTCTGCC[A/G]GGTAAGCCACTAGCT | 10533 |
| rs370328305 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11544649 | TCCTTCTGGGCCCTG[A/G]AGTCCAAGGGCCTGA | 10533 |
| rs370328626 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520560 | GATGCCGTGCTGGCC[C/T]TGGAGGAACACACAC | 10533 |
| rs370332493 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288629 | TCTCCCCACACTCCT[C/T]TCTCCTCACCTCCTA | 10533 |
| rs370364227 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436557 | TATATGTGTGTGTGT[A/G]TATAAATATAGCCCA | 10533 |
| rs370367181 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381925 | AAACCCAACATTAAT[A/G]CTTTAAAATGACAAA | 10533 |
| rs370372706 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11411947 | TGTGGATATCCAGTT[G/T]TCCCAGTATCATTCA | 10533 |
| rs370374329 | snp | C/G/T | 0.000153008 | 0.00874547 | intron-variant | ATG7 | GRCh38.p7 | 3:11362970 | TTTAAACAAAGCTTT[C/G/T]GTAGGCAGTTGTTCA | 10533 |
| rs370406467 | snp | A/C | | | intron-variant, missense | ATG7 | GRCh38.p7 | 3:11450192 | ATTAAGGCACATGGA[A/C]CCTAAGTGTTCAAGG | 10533 |
| rs370420463 | snp | G/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271239 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 10533 |
| rs370428400 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374696 | AGATCGTGAGGTCAG[A/G]AGATTGAGACCATCC | 10533 |
| rs370428765 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524567 | AGTTCGAGACCAGCC[C/T]GGACATCATGGTGAA | 10533 |
| rs370447787 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337848 | TCTTATTTTTGTCTA[A/G]TAATTTCTTACCTGT | 10533 |
| rs370458878 | snp | C/T | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557591 | ATATCAAATACCAAT[C/T]TTAGAGTACAACTGT | 10533 |
| rs370533656 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11457398 | AATGACACACACAAG[A/G]TAGAGGCTGTGCTTC | 10533 |
| rs370568365 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11301085 | AGCGAAGGACACAGG[C/G]GTTGTCAGAGGAAAA | 10533 |
| rs370568369 | snp | A/G | 1.66551e-05 | 0.00288571 | intron-variant | ATG7 | GRCh38.p7 | 3:11426952 | AACAAGCTTTCTGTA[A/G]TGAAGACTGACATGC | 10533 |
| rs370569693 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488584 | CCACCATGGCCGGAC[A/G]GGCTCCCTAAGCCAC | 10533 |
| rs370583564 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277693 | AGGGTCTATGTTCAG[A/C]AGTGTATGTATTGTC | 10533 |
| rs370602291 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395051 | CAAATTTTAGTTGTA[C/T]TGGGGACTGGAAACT | 10533 |
| rs370614832 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334105 | CAAAGTCAGAGCACG[A/T]TGTCTGGCACATCAT | 10533 |
| rs370623513 | in-del | -/ACC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408706 | AACGCCTCGTTAAAA[-/ACC]CTGCCATATCTTGTG | 10533 |
| rs370626064 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523563 | TCAGGGAGTCCTAAA[C/T]GTTGATTTGCCTTTG | 10533 |
| rs370663186 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11321442 | CCAGCATGCAGCTGG[A/T]CACTCATACATGTTA | 10533 |
| rs370663573 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456850 | CTGAAAGTGCTTGTC[C/T]TCTCTGAGGCCCCAG | 10533 |
| rs370676913 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359811 | AATTCTATGTGAAGG[A/G]TGAATTATATGGTAT | 10533 |
| rs370690554 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348146 | ATCTGTCACTTTCTA[C/G]CAGCCACTCGCTATG | 10533 |
| rs370712928 | in-del | -/ACACAT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515714 | CTCTCTCATACACAT[-/ACACAT]CAGTTTTATCACATG | 10533 |
| rs370728356 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341922 | CTGGAACTCAGTATC[A/T]AATCTGTGGCCCCCT | 10533 |
| rs370730698 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325540 | GCCGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 10533 |
| rs370749905 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527094 | ATATATATATATATA[C/T]ATACATATACATATA | 10533 |
| rs370762942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481484 | ATTTCACATTTCTTA[C/T]ATTTTACGTGCAGGT | 10533 |
| rs370790924 | in-del | -/TCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528195 | GTTTTCTGCACTGAA[-/TCT]TCTTTATAGCCTGCA | 10533 |
| rs370809372 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11301327 | TTTTTTCTGCTTTAT[G/T]GTACCTCAGCAGTAT | 10533 |
| rs370839699 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486988 | ACCCTGCGGCCTTCC[A/G]CAGTGTTTGTGTCCC | 10533 |
| rs370848056 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413655 | TGTTATTTCATTGAG[C/G]ATTTTTGCATTAATT | 10533 |
| rs370850653 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11333153 | GAAACGGAACCAGGT[C/T]TACTTTCTTTTCATA | 10533 |
| rs370860407 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486993 | GCGGCCTTCCGCAGT[A/G]TTTGTGTCCCTGATT | 10533 |
| rs370865102 | snp | C/T | 6.59055e-05 | 0.00574007 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306972 | CAGCCCGTTGCTGCC[C/T]AGCTATTGGAACACT | 10533 |
| rs370893584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11541188 | TACAGGCGTGAGCCA[C/T]CGCGCCCGGCTGGTT | 10533 |
| rs370910174 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506587 | AAAAAAAAAAAAACC[-/C]AAAAATTAGCTGGGA | 10533 |
| rs370917723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325434 | CACAGCACTTTGGGA[A/G]GCCAAGGTGGGCAGA | 10533 |
| rs370931461 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294761 | ACTATCCCTTCTCTT[A/G]TCGAATCTTCTTTCC | 10533 |
| rs370932803 | snp | C/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308371 | AATTTGAAGTTTGTT[C/G/T]TTCTTTCTTCATCTC | 10533 |
| rs370940788 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529362 | AAGCTGCTTGCCCCT[C/T]CTACCACAAGCAGTA | 10533 |
| rs370961216 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11333822 | GCGTGATCTTGGCTC[A/G]CTGCAAGCTCCGCCT | 10533 |
| rs370969788 | in-del | -/ATATTAT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334550 | AGCCTGGCCTCATAT[-/ATATTAT]TTAGCTTGTTCCTTA | 10533 |
| rs370974743 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293383 | AAAAATATAAAAAAT[C/T]AGCCGGGTGCGGTGG | 10533 |
| rs370974826 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285186 | CTTTTTTTTTTTTTT[A/T]AATTCCTTCCTGTGA | 10533 |
| rs370985902 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381824 | GCTTCATTGGTGCAC[A/G]TATTTCCTTACAGTA | 10533 |
| rs370990097 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11316556 | ACTGCATTTATTCCC[C/T]GATCCTCATTTGCAG | 10533 |
| rs370992506 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501547 | AGATAATGATATTAA[-/TT]TAGATAGGTGTGATA | 10533 |
| rs370997455 | snp | C/T | 3.36005e-05 | 0.00409867 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11362890 | TGCAGGAGCCCTGGC[C/T]GTGGAATTGATGGTA | 10533 |
| rs370998823 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11407618 | GGGCATCCAGGTGTT[G/T]CCATACATCTTCTGA | 10533 |
| rs370999499 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397857 | GGAGCCTGAGGTGGG[C/T]GGATCACCTGAGGTC | 10533 |
| rs371002887 | snp | C/G | 1.65187e-05 | 0.00287386 | intron-variant | ATG7 | GRCh38.p7 | 3:11307068 | CAAATGAGGTTAGCT[C/G]TGAAAACGTGATGTA | 10533 |
| rs371008707 | snp | A/G | 7.07827e-05 | 0.00594864 | intron-variant | ATG7 | GRCh38.p7 | 3:11358628 | GTAGGCCCTGTCTCT[A/G]ATTATGATTTATGAT | 10533 |
| rs371022267 | snp | C/T | 1.67069e-05 | 0.00289019 | intron-variant | ATG7 | GRCh38.p7 | 3:11342286 | ACGTTGATGGTAAGT[C/T]GGAGGTGGGGGGTGC | 10533 |
| rs371035892 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372123 | AACCTGGTGCCCCAC[A/G]TCTGACAACAGGGAT | 10533 |
| rs371036807 | snp | A/C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515251 | AGTGTGTTCATGTCT[A/C/T]AACTGAGAGGTGGTG | 10533 |
| rs371046819 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11545459 | GCCTCCCATCCTCGG[-/C]TCCCGGCTGGAGAGT | 10533 |
| rs371068440 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11377028 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTTGTC | 10533 |
| rs371068488 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330423 | CATCATATTATTTAT[A/G]TTGTTGCACAAATTG | 10533 |
| rs371069072 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ATG7 | GRCh38.p7 | 3:11488439 | CGGTCGGGCAGCGGC[A/G]GCTGCGGTCGGTCGC | 10533 |
| rs371071293 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397128 | AATGCTGGCGGTAGA[A/G]AGATTATCAAACCAG | 10533 |
| rs371075698 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11550632 | TGAACTCCTGGGCTC[A/C]AGTGATCCTCCCGCC | 10533 |
| rs371081519 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373073 | GTTAACTTTTTTTTT[-/T]GAAAAGCTGTTTAAT | 10533 |
| rs371083976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355133 | GTACTCACAGCACGA[C/G]TCTCGTCAGACCAGG | 10533 |
| rs371087797 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311436 | TAGTTAAACCCCGTA[C/T]CTACTAAAATTAAAA | 10533 |
| rs371092544 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11412245 | CTGTGATCTGATGAG[A/C/T]TCCAGTTATTTGATT | 10533 |
| rs371102575 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331346 | TGTTCACAGATAACA[A/G]TTGGTGTATATGATC | 10533 |
| rs371122185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460454 | CATGACTGAGCAACA[A/G]TGCCTGATGTGGGCA | 10533 |
| rs371125496 | snp | A/G | 0.000100236 | 0.00707868 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358436 | GCCAGAGGATTCAAC[A/G]TGAGCATACCTATGC | 10533 |
| rs371132095 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439050 | TCTTAGTCTTATTTT[C/T]TTTTTCTTTTCTTTC | 10533 |
| rs371155483 | in-del | -/CTTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551753 | GGGTTCTTTTCTTTT[-/CTTTT]TTTTTTCTCGAGGCA | 10533 |
| rs371157952 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11320464 | GGCTAATTTTTTTAT[A/C]TTTAGTAGAGATGGG | 10533 |
| rs371161802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443893 | AGTATGAATTAAACA[A/C]CCAGGTCAAAAAATA | 10533 |
| rs371190525 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389691 | CACAAGGGTGTATTC[A/G]GCAGAGTCTTGAGTA | 10533 |
| rs371208293 | snp | A/G | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342224 | AGGTTGTGTCTGTCA[A/G]ATGTCTGCTGCTTGG | 10533 |
| rs371214163 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453080 | TGGAGAATCTACAGC[C/T]CTGTCCACCACGCCT | 10533 |
| rs371224715 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471517 | TGTCTCCATTTTGCA[A/G]ATGAAAATAAGAAAC | 10533 |
| rs371237937 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11447750 | CTGTGATTGGCCAGG[C/T]CTGGGTCACATGCCA | 10533 |
| rs371263733 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332093 | AAGAATGTTTACAGA[A/C]GCATTATTCTCAATA | 10533 |
| rs371270709 | in-del | -/ACACACAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478991 | CTGTATATTTACAAC[-/ACACACAA]ACACACACACACACA | 10533 |
| rs371314877 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553606 | GACCTGACCCAGAGA[C/T]AGGGACACCTGGTCA | 10533 |
| rs371326693 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11483720 | TGACACTGGAGCCAA[A/T]TAGGAAATCGGAGGA | 10533 |
| rs371329929 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516047 | AAAAAAAAAAAAAAA[-/C]AAAAAAACATAGGAC | 10533 |
| rs371330517 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551159 | CTCGTTTCTGTACTC[C/G]TCGTGTCCTGCGGGC | 10533 |
| rs371331295 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440344 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTCGCTC | 10533 |
| rs371347924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444674 | CAGGCAAAAATTTCA[C/T]GATGATGCCAAAAAC | 10533 |
| rs371358393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11405365 | ACTATGGAGCTTGAG[A/G]GGGTGAGGCGATGAG | 10533 |
| rs371363734 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11510950 | CGCGGTGAGTGTTAC[A/G]GCTCTTAAGGTGGCG | 10533 |
| rs371364711 | snp | C/T | 0.000817884 | 0.0202058 | intron-variant, synonymous-codon | ATG7 | GRCh38.p7 | 3:11510226 | GAATGGCACCTTCCC[C/T]GCCCATCAGGCCACC | 10533 |
| rs371367627 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11535851 | CTTGAATGGTGAAGC[A/T]TATCAGTCCTTTTTA | 10533 |
| rs371374499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485973 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 10533 |
| rs371376688 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493810 | GCACAATCTGGGGCA[C/T]CACAAAGAGATTCGG | 10533 |
| rs371381130 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11540145 | CAAATTCACTGTGTC[A/G]TTTTTGCTGTTGCCA | 10533 |
| rs371381710 | in-del | -/GAAATGCAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530507 | ATGCAAGAAATGCAA[-/GAAATGCAA]AGATAAATACAAGAA | 10533 |
| rs371393731 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473488 | AATGTTTTAGAACGG[A/G]TGGAAAAACTCGGGA | 10533 |
| rs371395015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374835 | TGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 10533 |
| rs371408342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495998 | CACTTTCCACATGGT[A/T]GCCCTATGACGTAAG | 10533 |
| rs371418568 | in-del | -/GA | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557876 | TGAAATCTAGAGAGA[-/GA]AAGACCTATAACCTG | 10533 |
| rs371423496 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487872 | GCCGGGCGGAGGGGC[-/A]TCCTCACTTCTCAGA | 10533 |
| rs371440091 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458099 | TGGAACTAGTGTCTT[A/G]TTTTCAAAACAGCCC | 10533 |
| rs371442552 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326839 | TTCTCAGAGTTCTCT[C/G]ACTTCTCATCCGAAG | 10533 |
| rs371453665 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516502 | CATTGCTGGTGGGAA[C/T]GCAAAATGGCACAGC | 10533 |
| rs371471850 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326730 | AAAAAGATGTCCCTG[A/G]TGGAAGAGTAGCAGG | 10533 |
| rs371491069 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322868 | CTCTGGGAGACCTAG[G/T]TGAGAGGATTGTTTG | 10533 |
| rs371492021 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394921 | AGGTACCATAAGTGA[C/G]AGTTGGCAGAAGCAA | 10533 |
| rs371564550 | snp | A/T | 5.10365e-05 | 0.0050513 | intron-variant | ATG7 | GRCh38.p7 | 3:11333132 | GCATATAATTATCAT[A/T]TATCAGAAACGGAAC | 10533 |
| rs371573119 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11525616 | CTGGAGTGCAGTGGC[G/T]TGATCTCGGCTCACT | 10533 |
| rs371573922 | snp | A/C/T | 0.00597694 | 0.0544006 | intron-variant | ATG7 | GRCh38.p7 | 3:11337629 | TCTAATTTTCTTAGA[A/C/T]ATGGCTATAGCCTTT | 10533 |
| rs371576626 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322467 | TGTTTTTAAAATGTC[G/T]CAAAGGTTTTCAGCT | 10533 |
| rs371591489 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555178 | GGGGGTGACCCAACA[C/T]AGACCAAATGGGGAA | 10533 |
| rs371594313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369998 | GTTTGACCTTGGGCA[C/T]GTTACGTATCTTCTC | 10533 |
| rs371596449 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486475 | ATATACAACCATGTC[A/G]TCTGCAAACAGGGAC | 10533 |
| rs371605149 | snp | A/G | 3.31994e-05 | 0.00407414 | intron-variant | ATG7 | GRCh38.p7 | 3:11554783 | GCAGTGGGACATCTC[A/G]GCTGAGCCTCTCCCC | 10533 |
| rs371616859 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11323773 | TCTTCACTTAGTGAT[C/T]TCTCCGCATCTTGGC | 10533 |
| rs371618258 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11320455 | ACCACACCTGGCTAA[A/T]TTTTTTATCTTTAGT | 10533 |
| rs371625415 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348743 | CCTGATTTGTCCCCA[C/T]CCACGTCCTACTGAT | 10533 |
| rs371668629 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11340152 | TCAAATGACAGTCAC[C/T]TTGGACTGTGATCTG | 10533 |
| rs371679942 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11310045 | GTGGCGCCTGCCTGT[A/G]GTTCCAGCTACTGGG | 10533 |
| rs371695750 | snp | G/T | 3.29788e-05 | 0.00406058 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298865 | ACAATGGTAGGTGAT[G/T]GTAAATTTCATTTTC | 10533 |
| rs371715997 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404802 | GTGGAGGGGAACTCC[C/T]TTTATAAAACCATCA | 10533 |
| rs371716073 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344127 | GGGATGTAGGAAAAA[-/TA]GTGAATTTTGCATAT | 10533 |
| rs371719722 | snp | C/T | 6.59044e-05 | 0.00574002 | intron-variant, missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11379990 | CGGGGATTTCTTTCA[C/T]GGTTTGATAATGTCC | 10533 |
| rs371740273 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284803 | GATCATCCTGCTTTG[G/T]CCTCCCAAAGTGCTA | 10533 |
| rs371745627 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11522344 | CATGTATTTTTAGAA[A/C]TGCCCACCTTTTGTG | 10533 |
| rs371753696 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462948 | TGGAGTGTAATGGTG[C/T]GATCTCTGCTCACTG | 10533 |
| rs371763044 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448970 | GAAACCTGGAATTAG[G/T]GTAAAAATGTCACAC | 10533 |
| rs371768007 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461222 | AAATGCAGAGACAGC[C/T]TGCACTGGCATTTTA | 10533 |
| rs371769422 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11310995 | TCTAGTTACTTGAAC[A/G/T]TCAGTACGCTTTCTG | 10533 |
| rs371773280 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507899 | CACATGGGGTGTAAG[C/G]CATGCTGGGAAACAC | 10533 |
| rs371776756 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465440 | ACAGAGAGAGACTCT[C/G]TCTCAAAAAAAAAAA | 10533 |
| rs371784722 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11327966 | GAGGAGTATGGGAAG[A/G]TGTAGGGCCAATCCA | 10533 |
| rs371789644 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389806 | TCGTCATAAGTCTTG[A/G]CAGCTAAGGTGTCTT | 10533 |
| rs371804134 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278031 | ACAAAAATATGGCTG[G/T]ATTCTGCCTGACCCT | 10533 |
| rs371811177 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284263 | TATTTGCTGTGTCCA[A/G]TCCTAGAGGGAGAAT | 10533 |
| rs371811319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11308002 | CAGGCCTTAATCATC[C/T]TGGAAAAAAGCAGGC | 10533 |
| rs371823483 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11364931 | GAGGAAATCACGAAC[A/G]AGAAGCATTGCCCAG | 10533 |
| rs371830757 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478145 | GTCTTGTTAGAGACA[C/T]TATTAGTATGACCCC | 10533 |
| rs371835032 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540917 | TTTTTTGGGGGGGGG[A/G]GGGGGGGAGTCTTGC | 10533 |
| rs371850503 | in-del | -/T | 0.0441957 | 0.141932 | intron-variant | ATG7 | GRCh38.p7 | 3:11410331 | GTGAATGATATTGTA[-/T]TTTTTTTTAAATTAA | 10533 |
| rs371854424 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11323836 | GTATTTCAGTTTTTT[-/C]CCCCATACTTTAAAA | 10533 |
| rs371855056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542377 | CCTAGAGCAGCCTGT[C/T]GCTGTGGGCTGGGAA | 10533 |
| rs371867109 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531189 | CTAAAACCCCGTTGT[G/T]CTGCCCCAGGTCTGG | 10533 |
| rs371884021 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11352413 | CTAGTTCTAGATCCT[C/T]GAGTAATCGCCACAC | 10533 |
| rs371884968 | snp | A/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271242 | TTTTTTTTTTTTGAG[A/T]CGGAGTCTCGCTCTG | 10533 |
| rs371956569 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502531 | TTTCCAATTTCATCC[A/G]TGTCCCTACAAAGGA | 10533 |
| rs371984488 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525556 | TATCTAGTTATAGCC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs371987302 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395756 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 10533 |
| rs372000482 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11364509 | CTTCTTGCCCTTTGT[C/T]CCAGGGAAATTAGTT | 10533 |
| rs372004394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462487 | GGGTTTCCTTGGAAA[A/G]GTCAAGGCAGGGCAG | 10533 |
| rs372010423 | snp | C/G | 1.71496e-05 | 0.00292822 | intron-variant | ATG7 | GRCh38.p7 | 3:11313254 | ATAGATGCATTTCAC[C/G]TTAAGTTAATGGTGC | 10533 |
| rs372037823 | snp | A/G | 1.68471e-05 | 0.00290228 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333032 | TACCATGCAGGGGGC[A/G]AGAGACGTTGCCCAC | 10533 |
| rs372059003 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270495 | CTGTCTCATGTGTCC[A/G]TGTGAAGAGACTACC | 10533 |
| rs372080963 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11531764 | AGCTACTCGGGAGGC[A/T]GAGGTGGGAGGATCA | 10533 |
| rs372088418 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471703 | ACTCTTTTTTTTTTT[-/T]AGAACTCAGAAAAGT | 10533 |
| rs372210117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374617 | GTGCTTCAAGAAAGC[A/T]CAAAAAGTCCATGTG | 10533 |
| rs372234524 | snp | C/T | 1.64885e-05 | 0.00287123 | intron-variant | ATG7 | GRCh38.p7 | 3:11364645 | GAGCAGCTCTGATTG[C/T]TTCCTGTCCTCAGGG | 10533 |
| rs372262212 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510573 | TCTTTGTGCAACTCG[C/T]CGCCCACATCCAGCA | 10533 |
| rs372271982 | snp | C/T | 1.65809e-05 | 0.00287926 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333053 | CGTTGCCCACAGCAT[C/T]ATCTTCGAAGTGAAG | 10533 |
| rs372276665 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478674 | TTAAATAGAAAAAAG[-/C]CCCAAAAGGAAAGGA | 10533 |
| rs372284621 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353473 | AAAAGTTTAAATTTT[C/G]AAATAGTAAATTCAT | 10533 |
| rs372288030 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11494917 | TCTGTACTAAAAATA[C/T]AAAAATTAGCTGGGC | 10533 |
| rs372304104 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406321 | TTGCCATGTTTTTTT[-/T]GAGACAGTTTCTTGC | 10533 |
| rs372304129 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11375915 | GTTCCTCAAAATGTT[A/T]AACAGTCGTCATATG | 10533 |
| rs372306629 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11360114 | GCAGTGGCGGAATCT[C/T]GGCTCACTGCAAACT | 10533 |
| rs372353369 | snp | A/G | 3.31109e-05 | 0.00406871 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554826 | ATCTGGGACATGAGC[A/G]ATGATGAGACCATCT | 10533 |
| rs372380466 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408979 | TAAGATCTTTGGCTC[A/G]TTTTTTAATTGGGTT | 10533 |
| rs372393825 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ATG7 | GRCh38.p7 | 3:11393297 | TGAGGAAATCCTCTA[A/G]TATAGATTTCAAAGC | 10533 |
| rs372394336 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11303845 | TTTGGGAGGCCGAGG[C/T]GGGTGGGTCACGAGG | 10533 |
| rs372399326 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357306 | ATATTATGTGGTCAT[C/G]AAGGGGCAGATGGTA | 10533 |
| rs372412959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11551716 | ATTACAGGCACGAGC[C/T]GCTGTGCCCAGCCAA | 10533 |
| rs372420637 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381087 | TTTTCTTTTTGCTTC[C/T]GAAGTAAACTAAGCC | 10533 |
| rs372430052 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11380909 | AATTCTAGGGATGTA[C/T]TTCTCTATTCTGAGT | 10533 |
| rs372440405 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11521092 | GGAACATGGTAAAAA[A/T]GCCTGTCTCGCAGCA | 10533 |
| rs372441187 | snp | C/T | 6.62658e-05 | 0.00575574 | intron-variant | ATG7 | GRCh38.p7 | 3:11360568 | CTGCTCTTTCATTCC[C/T]TGAAACCTGCAGCTG | 10533 |
| rs372502938 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11333483 | GTGATCCTGTTCTTC[A/G]TATAGTAAACCAGTC | 10533 |
| rs372516483 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532218 | TTTGTTGAGCATTTA[C/T]TGATGCAATGCACCA | 10533 |
| rs372516573 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439065 | CTTTTTCTTTTCTTT[C/T]TTTCTTTTTTTTTTT | 10533 |
| rs372530056 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376824 | GCTCACTGCAAGCTC[C/T]ACCTCCCGGGTTCAC | 10533 |
| rs372530104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396639 | AACTAAAGTTTAGCC[A/G]GGCATGGTGGCAGAC | 10533 |
| rs372552559 | microsatellite | (CA)21/23/24/25/26/27/28/29/30 | 0.86173 | 0.0511263 | intron-variant | ATG7 | GRCh38.p7 | 3:11475870 | TCTCTGTCTCTGAGA[(CA)21/23/24/25/26/27/28/29/30]CCTCCCAGAGTCCGA | 10533 |
| rs372553907 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381564 | TGGGCGTTCCTTATA[-/TA]CTTTAAAAGAGAATA | 10533 |
| rs372596436 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553331 | GAAAGAGGGAGTATT[C/T]GCAGCAGGTCTACAC | 10533 |
| rs372599577 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11541191 | AGGCGTGAGCCATCG[C/T]GCCCGGCTGGTTTTA | 10533 |
| rs372651539 | snp | C/T | 0.000234905 | 0.010835 | intron-variant | ATG7 | GRCh38.p7 | 3:11315326 | TCTAGAGAATAACAA[C/T]GTGTTTTCTGTTTTC | 10533 |
| rs372654615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276706 | GTCCTACTTTGTATT[A/C]TCTCTCTGGCCATTT | 10533 |
| rs372716059 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11290254 | AGAAAGGCAGTGACT[A/G]AGGCCCTTTCCTCTT | 10533 |
| rs372725130 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11494782 | CATGCACTCTGTAAA[C/G]GCTTGAACAGGCCAG | 10533 |
| rs372741203 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406000 | TTTGTTTTTGTTTTT[G/T]TTTTTTGTAGATGGA | 10533 |
| rs372747923 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528455 | AGACCTTGAGAAGCC[C/T]ACAGAGAAAAATGCT | 10533 |
| rs372786063 | in-del | -/TGTATATA | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527070 | GTGTGTGTGTGTGTG[-/TGTATATA]TATATATATATATAT | 10533 |
| rs372845176 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350037 | GAGCATTTGCTTATA[C/T]TTAAAGTGCCAGAAG | 10533 |
| rs372856416 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11443298 | TCCCTTGAAAAATGA[A/G]TTCTGGCTCACTCCT | 10533 |
| rs372857027 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271366 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 10533 |
| rs372879728 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11478352 | GTTTCAAATGATTGC[C/G]TAATCTTACCTGTAA | 10533 |
| rs372883070 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369030 | GACCCTGGGAGGGAC[C/G]TGGCCTGGGAAAACT | 10533 |
| rs372883269 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11459026 | TCATTCATCACCCCC[C/G]CATCTATGGAAAAAT | 10533 |
| rs372889554 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550120 | TAAATACAAGTTCTT[C/T]TAATATAGAGATATT | 10533 |
| rs372891033 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339818 | CAAATCAAATCACGT[A/G]GGTTCTGTACTGCAG | 10533 |
| rs372904207 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417816 | TTTTATTTTATTTTA[-/T]TTTTTTTTTTTTTGA | 10533 |
| rs372904554 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490373 | TGTGTGTCTCTGCAC[G/T]TGACATGGGTTTCCT | 10533 |
| rs372914250 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11482910 | CACCCAGATTGGGAG[A/G]TAGAACATTTCCAGG | 10533 |
| rs372923104 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410608 | TTTTCTTCTCTCTCC[A/C]GCCCTGCCAGCCACT | 10533 |
| rs372932112 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11299912 | CTGTGGGGAGTTGCT[A/G]GAGAGAAGAGACACA | 10533 |
| rs372951608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11461749 | TGTGGACTCTGGGCC[A/G]GGCGCAGTGGCTCAC | 10533 |
| rs372953735 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459173 | GAGGGGGAGTCACTT[A/T]AAAAAAAAAAAAAAA | 10533 |
| rs372960182 | in-del | -/ATCCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499260 | TTGCCACATTCCTCT[-/ATCCT]TTCCTGTTCTACATG | 10533 |
| rs372965860 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11318645 | GGTTCCTGTTGACTT[C/T]GGGATAACGTTAAAA | 10533 |
| rs372988859 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11546841 | AGTGGGGAGCGCTGA[A/G]GTGCTCAGGTCAGGC | 10533 |
| rs372998209 | snp | C/T | 4.94352e-05 | 0.00497143 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358496 | ACTCTGGAGCAAGCC[C/T]GCAGAGATGTGGAGC | 10533 |
| rs373021192 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394531 | GAAGTTGAGAGCGTG[A/T]GCCACACCTTTAGTG | 10533 |
| rs373031751 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288494 | GTCTTTTATCTCTCT[-/CT]TTGTCTTCTTGCCAT | 10533 |
| rs373033377 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11435361 | CTCGGTGCCACTTTT[G/T]ACTTCTTTATAAACT | 10533 |
| rs373039430 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365564 | AATGTGACTGCTGTT[C/T]CCATCAGTGAAATCG | 10533 |
| rs373042796 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312354 | GAATTTAATTAAGGC[C/T]CCAAAAGCTGTAAGA | 10533 |
| rs373050917 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384210 | GACTGTGCAGGAGGA[A/G]ACTGCGTGCAGAGTA | 10533 |
| rs373060091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523825 | ACTAGAAAAAGTGAG[A/G]GGAAATCAGCCAAAT | 10533 |
| rs373077210 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277143 | TCCATTTCCTCCCTT[A/G]CTCCCTCATTTCAGG | 10533 |
| rs373087013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11397154 | ACCAGATTTTTAAAT[G/T]TATATGCATTATACA | 10533 |
| rs373101237 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392742 | CTTCATTTAGGAAAT[C/T]TGATGCACCACAATT | 10533 |
| rs373107280 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373816 | TGCTCTTTAAATTTT[A/G]TGCAGTTCTTATAAG | 10533 |
| rs373109190 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528053 | CGTGTGGTCCCTTCT[A/G]CTTCAATTGTGGGCC | 10533 |
| rs373111996 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11388725 | GAGCCACTGCGCCAG[A/G]CCCCTTCTTTCTTTT | 10533 |
| rs373113038 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480871 | GGCCTCTCTTCTTCC[C/T]AGTCCAGCATTAGAC | 10533 |
| rs373141011 | snp | A/G | 1.67298e-05 | 0.00289217 | intron-variant | ATG7 | GRCh38.p7 | 3:11360540 | CAGCTTGAAATATAT[A/G]TGTCTTTTAACTCTG | 10533 |
| rs373153232 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382202 | TGGGGAAGTAGAATA[A/T]GTTTCTGCTGAATAG | 10533 |
| rs373155999 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11537112 | GTGCTCTGCTGTCAG[C/G]CCCCCGGAGCCCCTG | 10533 |
| rs373158505 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488025 | GCGGCGGGGCAGAGG[C/T]GCTCCCCACATCTCA | 10533 |
| rs373179936 | snp | C/G | 0.40853 | 0.193309 | intron-variant | ATG7 | GRCh38.p7 | 3:11487766 | CAGCTCCCTCCCGGA[C/G]GGGGTGGCTGCCGGG | 10533 |
| rs373187047 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532800 | TTGTGGCAAGGATGG[A/G/T]TCTAGATACTGCATG | 10533 |
| rs373190438 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491292 | TTCTGCATTCTTCAC[A/G]TAGTTCTCAAGCCTT | 10533 |
| rs373192647 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11418081 | TCCCAAAGTGCTGGG[-/G]ATTACAGGCATGAGC | 10533 |
| rs373205372 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500057 | CATTTTAACATCTTC[C/T]GGGGATGCTGTAAAG | 10533 |
| rs373219309 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509360 | TACATCCAGGGAGCT[C/G]TTTTTTTTCTGATGC | 10533 |
| rs373224197 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | ATG7 | GRCh38.p7 | 3:11486257 | GAAGAGGTCCTTCAC[A/T]TCCCTTGTAAGTTGG | 10533 |
| rs373233928 | snp | C/T | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556233 | GCGCACTGCAGGCAG[C/T]GCGGCTCTGGGAAGA | 10533 |
| rs373259645 | snp | C/T | 1.81906e-05 | 0.00301579 | intron-variant | ATG7 | GRCh38.p7 | 3:11426788 | CTCCTTTTTAAAAAA[C/T]GTAAATGTTTTACAG | 10533 |
| rs373272349 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429249 | AGCTGTAATCCTAGC[A/C]CTTTGGGAGGCCGAG | 10533 |
| rs373293798 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | ATG7 | GRCh38.p7 | 3:11308929 | CACTTCACCTGAGAG[C/T]GAGAAACTCAGAGAT | 10533 |
| rs373296252 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484385 | GATGACAGGAGACTC[C/T]GTCTCAAAAAATGAA | 10533 |
| rs373313543 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500279 | AATTTGGTTGGAGTA[A/G]GGAGGTGGAGACATA | 10533 |
| rs373328336 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11310607 | TTGGCATTAATAATC[-/T]TGTCTATACGTTTGG | 10533 |
| rs373329304 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11291849 | GTAGAGAGGGGAAAG[A/G]TTTCCTAGGAACATC | 10533 |
| rs373363353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11552781 | GAGTGGCTCAATCTG[C/T]CCAGGAGCAAGGGGT | 10533 |
| rs373367113 | snp | G/T | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557017 | ACCGGGGGTCATACG[G/T]TGTGCAGAGTCCACA | 10533 |
| rs373372539 | snp | C/T | 0.000307953 | 0.0124049 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554862 | GGCCCCGCTGTGGGG[C/T]TGACTTCTCCCCGGC | 10533 |
| rs373375747 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11511943 | AGCTGGCCTGCAAGC[A/G]CCGCATGCAGCCCTG | 10533 |
| rs373377764 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11495073 | CAAGAGCAAGGCTCC[A/G]TCTCAGAAAAAAAAA | 10533 |
| rs373385945 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532135 | GCTGGGGTTCTTGCC[C/T]CCAAGGTTCCTAAGA | 10533 |
| rs373397424 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11544672 | GGGCCTGACGTGCTG[A/G]AGTCCTCAGAAGCCA | 10533 |
| rs373399299 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308871 | TTTGGGGTAAGTGGT[G/T]CTGGGCCTGTAGGAA | 10533 |
| rs373402365 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345876 | AATTTCAAAGTCAAC[A/G]TAAAGCCATTATAGA | 10533 |
| rs373410996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532707 | CAGTCTAGGTGACAG[A/G]GTGAGACCTGTCGTA | 10533 |
| rs373418309 | snp | C/T | 1.65811e-05 | 0.00287929 | intron-variant | ATG7 | GRCh38.p7 | 3:11306908 | CTGGCTGAGTCCCAG[C/T]TGTGCCTGACTAACC | 10533 |
| rs373427158 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508044 | CTAGTAGGATAAACA[A/C]CAGCCTCTACCACAG | 10533 |
| rs373429483 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376072 | CATGTGATACAATGT[C/G]GATGAAAATATGCTA | 10533 |
| rs373440227 | in-del | -/ATGCCTGGCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550551 | CAGACACATGCCACT[-/ATGCCTGGCT]CATTTTTAAAAAATT | 10533 |
| rs373447881 | snp | A/T | 1.78137e-05 | 0.00298438 | intron-variant | ATG7 | GRCh38.p7 | 3:11340756 | TTTGGGAAGCTGTTT[A/T]CTCCAGTCGGGCTTT | 10533 |
| rs373458651 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11347025 | TAGCCAGTCATGGCA[A/G]GACATCTCTTAGGTC | 10533 |
| rs373461651 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426864 | GTGTTTAATTCTTCA[C/T]ATTCCTTCTTAGAAG | 10533 |
| rs373531617 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271346 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 10533 |
| rs373541838 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359472 | CTAGCACTTTGGGAG[C/G]ATTGCTTGACCCAGG | 10533 |
| rs373543213 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386078 | GGTGGTGTGGAGGGC[A/G]GGAAGTCAGGGGATT | 10533 |
| rs373547057 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11355569 | TTGAACAGGTACTTA[A/C]TTTATGGTGAAGATC | 10533 |
| rs373547510 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299342 | CTTGTCATTGAAAAT[A/G]TGATAATGCTTCTGT | 10533 |
| rs373556753 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422382 | CTCACTTTTATGTTA[C/T]GGAGACAGCTTCTTT | 10533 |
| rs373567860 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468121 | CAGAAATTCAGCTAT[A/G]GAAGAGCGTGACTTT | 10533 |
| rs373592704 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11529912 | TTTCTTACTCACCCT[A/C]GCATGACCCATCTGC | 10533 |
| rs373643522 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11360238 | TTTTAATAGAGACAG[C/G]GTTTCGTCATGTTGC | 10533 |
| rs373652967 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473336 | TGAGTACCTGTTTTC[G/T]GTTAAGTATACCAAC | 10533 |
| rs373661465 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455132 | CAAAGTAAGGTATGC[C/G]TAAATATTCTTTTAC | 10533 |
| rs373662174 | in-del | -/TTTG | 0.061593 | 0.164325 | intron-variant | ATG7 | GRCh38.p7 | 3:11385017 | TGCTTAAATAGTGTT[-/TTTG]TTTGTTTGTTTGTTT | 10533 |
| rs373666042 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485041 | CAGCATGATTTATAG[C/T]CCTTTGGGTATATAC | 10533 |
| rs373669866 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11379831 | AGGGAAAATACTCAT[G/T]TCGAACTTATTTTTG | 10533 |
| rs373683223 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467152 | AAACAAACAAAAAAA[A/C]CTGATGGCTTCTTAA | 10533 |
| rs373687697 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11457846 | AATATTTTCCCTAGA[C/T]CTTGAGCTCCTTGAA | 10533 |
| rs373689783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11509546 | TATGAGCGTTTATAA[G/T]GGCCTTTTAAGTAAG | 10533 |
| rs373690738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11347781 | GTTTTGAGGTTCCCA[A/G]GCTTCTCCAAACCAA | 10533 |
| rs373695216 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447051 | TTTTCAGAGGGCATT[C/T]ACTTGCATTTACTCA | 10533 |
| rs373697077 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484774 | GTTCAATTCCCACCT[A/G]TGAGTGAGAATATGC | 10533 |
| rs373700075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11499671 | AGAATCGCTTGAACC[A/G]GGAAGGCAGAGGTTG | 10533 |
| rs373701101 | snp | A/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282214 | CAAACCCCATAATGC[A/T]GGTATCCAGTGCATC | 10533 |
| rs373713469 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501064 | GTTCAAGACCAACCT[C/G]GGCAACATAGCAAAA | 10533 |
| rs373714069 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278247 | AGAGATTAAAGACAG[G/T]CATAAGAAATTATAA | 10533 |
| rs373715882 | in-del | -/GAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517470 | GGCAGTGAATTAAAA[-/GAAAA]AAAACTCGATCCCTG | 10533 |
| rs373717660 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341900 | TCTTCCCTTTTCACC[C/T]TGGCTGCTGGAACTC | 10533 |
| rs373721865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311326 | TCGTGAGGTCCGGCC[A/G]GGTGCAGTGGTTCAT | 10533 |
| rs373725241 | in-del | -/G | 0.498503 | 0.0273153 | intron-variant | ATG7 | GRCh38.p7 | 3:11487711 | CCCCACCTCCCTCCC[-/G]GGATGGGGCGGCTGG | 10533 |
| rs373738298 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516544 | AAACACACTCTTACT[C/G]TGTGATCCAGCAATT | 10533 |
| rs373744114 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389465 | TTTTTTTAACACAGA[A/G]TAAGCTACATGGTTC | 10533 |
| rs373752475 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430522 | GGGTTAACTATTTAC[A/G]TCAATCAACATTGGA | 10533 |
| rs373755322 | in-del | -/CT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409587 | TAAGTTGATGAGCAT[-/CT]GTTTTTCTTTCATAG | 10533 |
| rs373761371 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490340 | TAGATCTTCCTCCAT[C/G]CTTTTATTTTGAGCC | 10533 |
| rs373763483 | snp | C/T | 8.31414e-05 | 0.006447 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11348029 | CCAGAAAATATTCCC[C/T]GGTGTGGTATGTTGT | 10533 |
| rs373791644 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540960 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 10533 |
| rs373804518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11554127 | GGTGGCTCTTGCTGG[A/G]TCCCTCAGTTCTCCT | 10533 |
| rs373815885 | snp | A/G | 0.000250855 | 0.0111966 | intron-variant | ATG7 | GRCh38.p7 | 3:11342287 | CGTTGATGGTAAGTC[A/G]GAGGTGGGGGGTGCA | 10533 |
| rs373834870 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336524 | TAGCTGTAAATAAAA[C/T]TTTATGGTAAATACA | 10533 |
| rs373835998 | snp | G/T | 0.000130421 | 0.00807424 | intron-variant | ATG7 | GRCh38.p7 | 3:11340772 | CTCCAGTCGGGCTTT[G/T]TGTAACCAAGACACA | 10533 |
| rs373847275 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11547789 | TTTGAGTATCATTTC[A/G]TGTGCTTCTTAGCAA | 10533 |
| rs373855035 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11274154 | GTACTGGACTTTCCA[G/T]TACTCAACCACAGGT | 10533 |
| rs373873013 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11497145 | AGTGAGCCCCCACGC[C/T]CAGCCCCTAATGTCA | 10533 |
| rs373881622 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452834 | CTATTCTTTTTAGTA[C/T]TTTTTTAAACACAAA | 10533 |
| rs373896065 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11482804 | TACCTTTTTTTTTTT[-/T]GAGGTTTATATCATT | 10533 |
| rs373896795 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286285 | GACTACTTTCATATG[C/T]AGTTGCATAAGGTTT | 10533 |
| rs373898774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391784 | CTTTCCAGTGTCTTA[C/T]GAATTGGCTAGCAAG | 10533 |
| rs373912916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11538260 | TGACCTGTCAGCTGG[C/T]TCAGGAAGGCCTTTC | 10533 |
| rs373920583 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519752 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACAGTGTT | 10533 |
| rs373921269 | in-del | -/TTT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11452404 | AGAACATTTCCTTTT[-/TTT]TTTTTTTTTTTTTTT | 10533 |
| rs373941355 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429904 | TGAGCTGAAATCGCG[C/T]GACTGAATTCCAGCC | 10533 |
| rs373969525 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11346698 | CAGTTGCTTTAAGGA[A/G]TGCAAAAATACTTCA | 10533 |
| rs373975090 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366108 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 10533 |
| rs373977100 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11388347 | CCTCAGAGTTCAGAC[G/T]GTTAGTTCTCCCTCT | 10533 |
| rs374004870 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440416 | TGCAAGCTCCGCCTC[C/G]CGGGTTCACGCCATT | 10533 |
| rs374013553 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341040 | ATTGTCCTCTAGCTT[C/G]GTCCTATTGGCCCAC | 10533 |
| rs374027192 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11358223 | TGCCTCAGGGCCCTG[C/G]GGTGATAGGTCAAGG | 10533 |
| rs374039584 | snp | A/C | 9.88614e-05 | 0.00703 | intron-variant | ATG7 | GRCh38.p7 | 3:11308933 | TCACCTGAGAGTGAG[A/C]AACTCAGAGATGCCT | 10533 |
| rs374043311 | snp | A/G | 9.90475e-05 | 0.00703661 | intron-variant | ATG7 | GRCh38.p7 | 3:11360801 | TAAGTGGATTTCTCT[A/G]TAGTTCCAAATATTT | 10533 |
| rs374047867 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11317604 | TTTTTTTTTTTTTTT[-/T]GTTTTTGAGGCAGAG | 10533 |
| rs374049181 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11403198 | TAGAGTCTGATAATT[C/T]GTAGTAAATGTAAAC | 10533 |
| rs374059786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11309675 | CTATGCATGCATGCG[C/T]GTGTGTGCGTACACA | 10533 |
| rs374089372 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11381746 | TTTAACAGCTGTGCT[A/G]TTCCCATAGCGGTCA | 10533 |
| rs374101727 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11355903 | TATACAAAAGTGTCC[A/G]TAGCACCTTTATTCA | 10533 |
| rs374125952 | snp | A/G | 0.000155902 | 0.00882762 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333016 | TTTGCTTCCGTGACC[A/G]TACCATGCAGGGGGC | 10533 |
| rs374142073 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306977 | CGTTGCTGCCCAGCT[A/G]TTGGAACACTGTATA | 10533 |
| rs374161778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11453998 | TCCGTGTAAATAAAT[A/G]TGACTGCCACTTCAA | 10533 |
| rs374163352 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342243 | TCTGCTGCTTGGAGC[C/T]GGCACCTTGGGTTGC | 10533 |
| rs374172828 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508107 | TGTTTTTTCAAAAAT[A/G/T]TGCTGTTTACTCTCC | 10533 |
| rs374177757 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371414 | TTGGAAATGCCTGGA[C/T]CTTCAACCCGGGGCC | 10533 |
| rs374186582 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311526 | AGAATTGCTTGAACC[G/T]GGGAGGTGGAGGTTG | 10533 |
| rs374190335 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472724 | TGGTAAATGCCTACC[G/T]CCCAGGACTTTTGAA | 10533 |
| rs374202679 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11338067 | ATCACCCAGGTACTA[-/AT]ACCTAGTACCTAGTA | 10533 |
| rs374220585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407916 | AAAGTTCTCTGACAT[G/T]CCCTGGAGGCATTTT | 10533 |
| rs374231663 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353160 | AAAATGTTTAAATTT[A/T]GGGCCGGGCACAGTG | 10533 |
| rs374239980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395815 | CGTGGTGGTGGGCGC[C/T]TGTAGTCCCAGCTAC | 10533 |
| rs374248570 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348316 | GAAGCCGCGGACCTT[C/T]GCAGTGAGTGTTACA | 10533 |
| rs374266079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511975 | TTCCCGCTCGTGCCT[C/T]TCCCTCCACACCTCC | 10533 |
| rs374272765 | in-del | -/GATTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400581 | AATGTGCAAGTACCT[-/GATTT]TTAAGTGTTGGTTCA | 10533 |
| rs374297479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11491800 | CGAATTTTTGTGAAC[C/T]GTGAATGCTGCTGTC | 10533 |
| rs374304852 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381538 | AAAAGAATCACAAGC[A/G]TACCATCTAACTGGG | 10533 |
| rs374312287 | snp | A/G | 0.000272324 | 0.0116657 | intron-variant | ATG7 | GRCh38.p7 | 3:11332958 | AATAAATAAAAATCC[A/G]GGCATGACAACAGGA | 10533 |
| rs374319818 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466083 | AACCTAAAGTCTGCG[A/G]CTTATTCCTAATGTG | 10533 |
| rs374327487 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438378 | GTAAAACATTTAGGA[C/T]TTGAAAAGATTACAT | 10533 |
| rs374337018 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11476895 | GCATCTGGATTAAAG[G/T]CTTCTTTTAATCTTA | 10533 |
| rs374343841 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11373949 | TTTTGTAAGCTTTGG[A/G]TTTTTGTTTACTTGT | 10533 |
| rs374348103 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | ATG7 | GRCh38.p7 | 3:11515651 | GGGCAGTGGGCTGCA[A/C/T]GGCCACATGTATACA | 10533 |
| rs374350824 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413011 | ATTAGTGCATAGAAA[C/T]GTAACTGGTTTTTAT | 10533 |
| rs374363299 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368414 | GAAGTTGGTTTGCCG[A/G]CTGGCAAGAGATCCT | 10533 |
| rs374367971 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488455 | GCTGCGGTCGGTCGC[A/G]GCAGCGGCTCCGCTT | 10533 |
| rs374375462 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466982 | AAATACAAAAAATTA[C/G]GTGTGGTGGCGGGCG | 10533 |
| rs374381643 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492366 | GCGCCCACTGTCTGG[C/T]ACTCCCTAGTGAGAT | 10533 |
| rs374472483 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417809 | ATTATTATTTTATTT[A/T]ATTTTATTTTTTTTT | 10533 |
| rs374475808 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512502 | TGTATTAGTACTTGT[A/G]TGTACAGAATTGGTG | 10533 |
| rs374498526 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11479113 | TCTCAATGGCAGGCT[C/T]CAGCATTGCCTTTGC | 10533 |
| rs374501135 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557662 | AAACTAATTCTGAAA[A/G]GAAGATAGTAAGTAT | 10533 |
| rs374501281 | snp | A/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271240 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTCGCTC | 10533 |
| rs374506077 | snp | A/G | 3.29549e-05 | 0.00405911 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331350 | CACAGATAACAATTG[A/G]TGTATATGATCCCTG | 10533 |
| rs374519384 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271149 | TCAGAGTGATCTCAC[C/T]ATTGCAATAGTCTCC | 10533 |
| rs374531536 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356688 | CCACCATTTAACATG[C/T]TTTGTCAATTGTAGT | 10533 |
| rs374533655 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11393717 | TCTCAGTCTCATTCG[A/G]TTGCCCAGGCTGGAG | 10533 |
| rs374543203 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365922 | TTGCACAAAACCACC[C/G]ATAATAGAACTTGTG | 10533 |
| rs374545532 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406005 | TTTGTTTTTGTTTTT[-/TT]TGTAGATGGAATCTC | 10533 |
| rs374550369 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439056 | TCTTATTTTCTTTTT[C/T]TTTTCTTTCTTTCTT | 10533 |
| rs374588113 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293573 | GAATGACTGGCCGGG[C/T]GGGGTGGCTCACATC | 10533 |
| rs374591354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11512594 | TTCTTAAAGCGGCAC[A/G]TCTGGAGTTATTTGT | 10533 |
| rs374594369 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11316258 | AATGGTGTCTTCCTT[C/T]TGGCTCCAAGCTGCC | 10533 |
| rs374595287 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271791 | TGAGTCTAGAGTGGT[A/G]TATCAGAGTTAATTT | 10533 |
| rs374602080 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11291526 | AGCTCCCAGTGTCTC[A/C]GTTTTCTCTTCAGTA | 10533 |
| rs374622174 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11431393 | AAGGGCGGGGGGAAA[A/G]AAACAACCACACACA | 10533 |
| rs374630084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334038 | ACAGGCATGAGCCAC[C/T]GCTCCCGGCCAGCTT | 10533 |
| rs374638570 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372126 | CTGGTGCCCCACATC[C/T]GACAACAGGGATTTC | 10533 |
| rs374668614 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499261 | TGCCACATTCCTCTA[C/T]CCTTTCCTGTTCTAC | 10533 |
| rs374681923 | in-del | -/ATA | 0.0376037 | 0.131863 | intron-variant | ATG7 | GRCh38.p7 | 3:11516331 | CCTAAAACTTAAAGT[-/ATA]ATAATAATAATAAAA | 10533 |
| rs374699633 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363851 | ACTCAAAGCTTTCCT[C/T]AGCAGTTGAAAATTG | 10533 |
| rs374719163 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11427923 | TTGGCAAAATGTGCA[A/G]TTCCTCAGAATTGAT | 10533 |
| rs374727241 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325765 | AAGAGCAAGTGATCC[A/T]GAATGTTTGATTAAG | 10533 |
| rs374759731 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11402791 | ACATTTTTTAACAAT[G/T]TTTTTAATGGAGTCA | 10533 |
| rs374781616 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11447462 | ACAGTGCAAGACTCC[A/G]TCTCAGGGAAAAAAA | 10533 |
| rs374791586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11342388 | CCATCCCCTCCATCT[C/T]TCCCTCCCTTCCTTT | 10533 |
| rs374799715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463002 | GCGATTCTTCCACCT[C/T]AGCCTCCCAAGGAGC | 10533 |
| rs374806102 | in-del | -/TTAGCC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538707 | AAAAAAAAAAAAAAA[-/TTAGCC]AAAAAAAAAAAAAAA | 10533 |
| rs374812052 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487310 | TCTATTCCACAAAGC[C/T]GCCATTGTCATCCTG | 10533 |
| rs374825239 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531184 | CAAGACTAAAACCCC[A/G]TTGTTCTGCCCCAGG | 10533 |
| rs374827254 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512995 | GTTCTCCAAGTCCCC[A/C]CCAGAGTAGCTAGAT | 10533 |
| rs374850934 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11321205 | AGATGAAGGAAAAGA[C/T]AGGAGTTAGCCTGCC | 10533 |
| rs374858057 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340232 | GGAACCTCAGTGAAG[C/G]GGTGCTGCAGTTACA | 10533 |
| rs374870685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358799 | AATGTAATAAGTACC[A/G]TTTACTGCTTAATTT | 10533 |
| rs374875589 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322871 | TGGGAGACCTAGGTG[A/G]GAGGATTGTTTGAGG | 10533 |
| rs374885992 | in-del | -/GT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465440 | ACAGAGAGAGACTCT[-/GT]CTCAAAAAAAAAAAA | 10533 |
| rs374909569 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419754 | AGTAAGGAGTCACCA[A/C]AGTGTCTTAGCAAGG | 10533 |
| rs374923893 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356790 | GGTACATAGTAGGTG[C/T]ACAATACTTAATGGA | 10533 |
| rs374932864 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376129 | TTTATAGTAAATAAG[C/G]AGAATAGGTAAAACA | 10533 |
| rs374941559 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378848 | TTTAAATAGTTTGTC[A/G]AATTGTTTGTTTTTC | 10533 |
| rs374959917 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant | ATG7 | GRCh38.p7 | 3:11380080 | GTATTGGAGGGACTT[A/G]TTTTTAAAAGTGAGC | 10533 |
| rs374977690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275008 | CAGGGGACCAGTTGG[C/G]TATAGTTGCAGTGAT | 10533 |
| rs374991564 | in-del | -/CAGT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11346839 | CAGTGGGCTTCAAAA[-/CAGT]CAGTCTAACCTATGC | 10533 |
| rs375008041 | snp | C/T | | | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313351 | TTGCTATCCTGCCCT[C/T]TGTCTTCCAGAGAGT | 10533 |
| rs375015734 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11543894 | GGTGACAGGCTGGGG[A/T]TGGAGGGTGGGCAGG | 10533 |
| rs375034929 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11323854 | ACTTTAAAAACGTGT[A/G]ATCTCCTTTGTGCAT | 10533 |
| rs375035827 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369222 | CATGGACAGATGGAC[-/A]TGCTGAGGAGGGAAA | 10533 |
| rs375036919 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279099 | CTAGCCTCCTCATCC[A/G]GGGGTCCTTGCATGG | 10533 |
| rs375038448 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303420 | CACGCCTGTAATCCC[A/C]GCACTTTGGGAGGCC | 10533 |
| rs375040664 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11504400 | ATGCAAACCATTGGA[A/G]GATGAACTCCAGAAA | 10533 |
| rs375055648 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461446 | CCTTAAGAGAAATCA[A/G]AAGGCTTTCACTTTT | 10533 |
| rs375070806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11505136 | TCATAACAAGCCTTG[A/G]AATTATTTGGCTCTT | 10533 |
| rs375073264 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273451 | CTCTTGGAATCACCC[C/T]TGCATTTAATTGCCC | 10533 |
| rs375086614 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462032 | TGAGACTCTGTCTCC[A/G]AAAAAAAAGAAAGAA | 10533 |
| rs375088586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441522 | GCTGGGATTACAGGC[A/G]TGAGTCACCGCAACC | 10533 |
| rs375101364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522345 | ATGTATTTTTAGAAC[C/T]GCCCACCTTTTGTGC | 10533 |
| rs375102135 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11431708 | GTTGTAGCAAGGTAC[A/G]CAATTGTTTTTCATT | 10533 |
| rs375148404 | in-del | -/TTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378027 | TATACCAGTTACCAA[-/TTTT]TTTTTTTTTTTTTTT | 10533 |
| rs375151805 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11345075 | TTGATGGTTAGGTAA[A/C]ATTCAGTTATAAATC | 10533 |
| rs375156407 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11483399 | CTGAGCTCCCAACAC[A/G]CACAGATCTTGCTTT | 10533 |
| rs375160639 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439069 | TTCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs375162033 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470029 | GAGAGAGATGGTGTA[A/C]TGGGCTGTGCGTGCT | 10533 |
| rs375174442 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444084 | AATTATGCTATAATA[C/T]GTAGATTCTTTCGTG | 10533 |
| rs375190308 | in-del | -/CC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277892 | GCGGCCCTTTATAGA[-/CC]CCCCCCCCCCCACCA | 10533 |
| rs375207201 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344278 | TAGAACTCCACAGTA[A/G]TGTAGAAGAATGGCA | 10533 |
| rs375212119 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11294984 | GGGCATGGTGGTGCA[C/T]ACCTGTAGTCCCAGC | 10533 |
| rs375232440 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11403748 | TAATGACCCTGAGGT[C/T]GAAGTATGAATATCA | 10533 |
| rs375254182 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415774 | TTTTTTTTTTTTTTT[A/T]AAATAAGTAGAGGGA | 10533 |
| rs375263150 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510881 | CTGTGGCTTTGTGTC[C/T]GGAATTGGTGGGTTC | 10533 |
| rs375264971 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286590 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 10533 |
| rs375272311 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270892 | CATCTGGATGTATAC[A/G]TGCAGGTCACTGGGG | 10533 |
| rs375280188 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485933 | AGTACCATGCTGTTT[G/T]GGTTACTGTAGCCTT | 10533 |
| rs375283029 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540640 | AGTGACACCCCATCT[A/C]AAAAAAAAAAAGTCT | 10533 |
| rs375287783 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500566 | AATTCTAGGCCATGT[A/G]GAAAATGATGTGAAA | 10533 |
| rs375296789 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542783 | CTGGGCTCTGTTCTT[A/G]GGAGTGAAGAAGGTG | 10533 |
| rs375326243 | in-del | -/TTGCATTGATG | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11501543 | TAATAGATAATGATA[-/TTGCATTGATG]TTAATAGATAGGTGT | 10533 |
| rs375326913 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557005 | AAAAACTGTAAAACC[A/G]GGGGTCATACGGTGT | 10533 |
| rs375332217 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493593 | CTTCTGCCTCCCTCA[A/G]TGGGTGATGCTAAAC | 10533 |
| rs375339991 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485974 | TTGAAGTCAGGTAGC[A/G]TGATGCCTCCAGCTT | 10533 |
| rs375346276 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467952 | GGCTAAATTTATATA[C/T]AGTAGCTGACTTGGA | 10533 |
| rs375419432 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492219 | GGGTGGGAGTGACCC[A/G]ATTTTCCAGTTGCCG | 10533 |
| rs375433048 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11301551 | GATTTTAGTATTTGT[A/G]TCTTTAAAAATGTAT | 10533 |
| rs375440292 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516576 | CACTCCTTGAGATTT[A/T]CCCGAATTAGTTGAT | 10533 |
| rs375444855 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11548743 | AGTCCAGGTGTGGAT[C/G]TGCATCAAATGGTTT | 10533 |
| rs375459611 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551607 | TTTTAAAGTTTTTAT[A/T]TTTATAGAGAGAGGG | 10533 |
| rs375524518 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453573 | TAATTTTTCTCATCT[C/T]AGTGATGTTCCAAGC | 10533 |
| rs375525124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11503543 | GTGGGCAGATCACGA[A/G]GTCAGGAGGTCAAGA | 10533 |
| rs375560548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11554529 | TGGCTGGGTCAGGGA[C/T]GGTCCCCCGAGGTGG | 10533 |
| rs375578811 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414704 | AGATGTAGAGATTTT[A/G]TGGATGTTCTTTATC | 10533 |
| rs375588906 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339314 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAC | 10533 |
| rs375589015 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478433 | CCTGAAGAGATGAGA[C/T]TGGCGCATATTAAAG | 10533 |
| rs375592807 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11497393 | TATATATATATATAT[A/T]TAGCCAGGCATGGTG | 10533 |
| rs375601935 | in-del | -/TCTCTCTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337483 | AGCTCTCTCTCTCTC[-/TCTCTCTA]TATATATATATATAA | 10533 |
| rs375606528 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371423 | CCTGGACCTTCAACC[C/T]GGGGCCCTGGGAGGC | 10533 |
| rs375618427 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11461890 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 10533 |
| rs375621937 | snp | A/G | 0.000437477 | 0.0147833 | intron-variant | ATG7 | GRCh38.p7 | 3:11362940 | AAGGGTGAGTTTGCT[A/G]GTAGGAGATGAGTAT | 10533 |
| rs375637771 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490470 | CATTTAGTCCATTTA[C/T]ATTTAAAGTTAATAT | 10533 |
| rs375646809 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11499773 | AAAAAAGAAACAAAA[A/T]ATCTAAAATATCCCA | 10533 |
| rs375651898 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300059 | CCTCCCAAGTAGCTG[G/T]GACTACAAGCTCACG | 10533 |
| rs375655889 | snp | C/T | 3.51958e-05 | 0.00419484 | intron-variant | ATG7 | GRCh38.p7 | 3:11340612 | TTTTATTCTTCCCTC[C/T]TTCATTAAACTTTGT | 10533 |
| rs375715694 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439503 | GGCTTCTATCAGTCA[A/G]CAGATATTTATTGAC | 10533 |
| rs375718785 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509659 | GGCCACCCCTCCCCC[A/G]ATCTATCTCTAATTT | 10533 |
| rs375731253 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517146 | GCATACTGAGTAATT[A/C]CACCTGTATGACATT | 10533 |
| rs375756427 | snp | A/G | 0.000267165 | 0.0115547 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333039 | CAGGGGGCGAGAGAC[A/G]TTGCCCACAGCATCA | 10533 |
| rs375757847 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11343675 | GGTTACATGATAAGG[A/G]GTAAAGATCTAGCTA | 10533 |
| rs375761041 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11433056 | CAGCACTTTGGGAGG[A/C]TAAGTTGGGAGGATT | 10533 |
| rs375768188 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11548412 | ACTCCAGTTTACTTA[C/T]TTTGTTGTTGCTTGT | 10533 |
| rs375772359 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478471 | TATGATGATGTGGCT[-/G]GTCATGGCTACATTA | 10533 |
| rs375783991 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11328184 | ATATTAGTAGCTCTA[C/T]GTATGTGCTGGACTT | 10533 |
| rs375791098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11510370 | CTTTGTAAGTTTGTC[C/T]CTGCCCCAGTTTAAA | 10533 |
| rs375802378 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284804 | ATCATCCTGCTTTGG[C/T]CTCCCAAAGTGCTAG | 10533 |
| rs375807359 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389457 | TTTTTTTTTTTTTTT[A/T]ACACAGAATAAGCTA | 10533 |
| rs375815245 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507476 | TTTGTAATTCCAAAG[C/T]AGTGATGAGTATTTG | 10533 |
| rs375826734 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396561 | GTGGGCGGATCACTC[A/G]AAGTCAGGAGTTTGA | 10533 |
| rs375842883 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426547 | TTTTCTAGAATTTTT[-/T]AGTGAATTTGCATGA | 10533 |
| rs375844346 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542001 | TTTAAAAATGTGTTT[C/T]GAAGCCTGGAAAAAG | 10533 |
| rs375860500 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350860 | GGGAGGCTGAAGTGG[A/G]AGGAGATCGCTTAAG | 10533 |
| rs375860562 | snp | C/G | 1.66899e-05 | 0.00288871 | intron-variant | ATG7 | GRCh38.p7 | 3:11426961 | TCTGTAGTGAAGACT[C/G]ACATGCTTAAAACTA | 10533 |
| rs375884513 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513424 | AGGGAGAAATTGAGC[A/G]CAGCACCAGTGGGCC | 10533 |
| rs375899505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11466494 | TGTCTCCCAGTGGGA[A/G]AAAAATGTAACTCCT | 10533 |
| rs375901682 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11541101 | GAGACGGGGTTTCAC[CA/TG]TGTTAGCCAGGATGG | 10533 |
| rs375909677 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11304046 | CAGTGAGCCGAGATC[A/G]CACGACTGCACTCCA | 10533 |
| rs375918763 | snp | C/T | 1.67576e-05 | 0.00289457 | intron-variant | ATG7 | GRCh38.p7 | 3:11333098 | ATTTAGCCCAGGTAA[C/T]TTGCCGGTCTTTGAA | 10533 |
| rs375920921 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367728 | TGAAAACCATAAACC[A/G]TTTCAGGTGAGCTTA | 10533 |
| rs375926036 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11322185 | AAATACCTGTTATAA[C/T]CCAATACATGTCTTT | 10533 |
| rs375930205 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485465 | CAGATGAGTAGGTTG[C/T]GAAAATTTTCTCCCA | 10533 |
| rs375942209 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500458 | CAATACAACWAAAAA[-/A]ATACAAATTAAAAGA | 10533 |
| rs375943082 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11505244 | TGGGTTTTTAAAGGA[C/T]GAGTAGGAGTTCTAT | 10533 |
| rs375946684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11429310 | AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCG | 10533 |
| rs375948441 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556294 | GGGGGCTTTCTCAGT[A/G]AAATGTTTGGTTTTC | 10533 |
| rs375963185 | in-del | -/GAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341390 | TGAAGGATATTAGAA[-/GAA]TTATTTCATGGAAGC | 10533 |
| rs375969341 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11524660 | AGAATGGTAGTGCAT[A/C]TCTGTAGTCCCAGCA | 10533 |
| rs375979488 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509819 | AATTTTCCCTGACTC[A/G]GTTGCTCCAGTGGTG | 10533 |
| rs375990144 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492063 | CCCCTCCCCCAGCCT[C/T]GCTGCCACCTTGCAG | 10533 |
| rs376022053 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523900 | TCTTCTGTTTCCACT[A/T]GTCTGGTAATAACTG | 10533 |
| rs376032682 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462503 | GTCAAGGCAGGGCAG[C/T]GTGAACACTTTAGGG | 10533 |
| rs376052801 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513650 | TCCCTGCAAGCTGAG[A/G]GAGCCAGCTCCAACC | 10533 |
| rs376053228 | snp | A/C | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557121 | GGTGGGACACAGCAC[A/C]CCCCAGGGGGAGGGG | 10533 |
| rs376053733 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553724 | TGGCCTCGGGAGACA[C/G]GGGCAGTGAGAAGGC | 10533 |
| rs376101737 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11521742 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 10533 |
| rs376113148 | in-del | -/AAAC | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11396955 | GATAGACTAAACAGT[-/AAAC]AAATAGAAAAATTGT | 10533 |
| rs376119720 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11518466 | GCAGGAGAATCTCTT[A/G]AACCCAGAAGGTAGA | 10533 |
| rs376134194 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529432 | TGGCTTCAAACAGAG[A/T]ATTGTTTTAAGTCTT | 10533 |
| rs376158049 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11354598 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 10533 |
| rs376162200 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464576 | TTTCCAAGAGTCATT[C/T]TTGTTTCTTGCCAAA | 10533 |
| rs376184201 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397830 | GCTCACACCTGTAAT[C/G]CCGGCACTCTGGGAG | 10533 |
| rs376206200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11352001 | TGCTATCCCTCCCCC[C/G]TCCCTCCACGCCACG | 10533 |
| rs376215194 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11316363 | CTCCATCCCCTTCCC[A/G]TCAGATACATCTAAA | 10533 |
| rs376215280 | snp | A/G | 9.88859e-05 | 0.00703087 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331340 | CTTTTTTGTTCACAG[A/G]TAACAATTGGTGTAT | 10533 |
| rs376257019 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394728 | ATTATTTAAGTGGCC[C/T]GGAAACCGTAAGGCT | 10533 |
| rs376266509 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311806 | GTTCATTTTGCCATT[C/G]TGAAGAGGGAATTTT | 10533 |
| rs376282056 | in-del | -/CA | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557965 | ACAACAACAAACACA[-/CA]AATGGTCAGAAATGT | 10533 |
| rs376289616 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411511 | CTGAGTCTCAGCTAC[G/T]CAGGAGCCTGAGGCA | 10533 |
| rs376293523 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351670 | AAGTCCCCCAGGCCA[C/T]GGTCCAAGTCTTTTA | 10533 |
| rs376307589 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474067 | ACTTAGTTGAGTTCA[C/G]TTCAGACTTACCAAG | 10533 |
| rs376322873 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441633 | GGTTTATCTGTACTC[C/T]GTTTCTTCCTTCCCC | 10533 |
| rs376323168 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490015 | GTGCAGAGCTGAGTT[C/G]AATTCCTGGGTATCC | 10533 |
| rs376325619 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461186 | TGAATAGACTTTTCT[A/G]AAATGAAGTGGAAAA | 10533 |
| rs376327753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11481444 | GCAAAATGTAAGTGT[A/G]TGTGACTTACCACAA | 10533 |
| rs376334451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319823 | AGCCTACCACCTTGC[A/G]TTTCTTCTGCCACCA | 10533 |
| rs376355547 | in-del | -/ATGACCCCCAAC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304467 | AGCATGACCCCCAAC[-/ATGACCCCCAAC]TGACTGTGACTTTCT | 10533 |
| rs376367189 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426271 | GGTTTCAGTTTTCAT[A/G]TCAACTACTCATGCC | 10533 |
| rs376370741 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338042 | AGGGGTTTGTTGTAC[A/G]GATTATTTGATCACC | 10533 |
| rs376371145 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11364990 | AGAGGCCTCATAATG[C/T]AATAGGAACAGAAAA | 10533 |
| rs376373008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11333461 | TGTTATATACTTAAA[A/G]TTGTATGTGATCCTG | 10533 |
| rs376391464 | in-del | -/GTTTTTTTTT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11506576 | CCAGCTAATTTTTGG[-/GTTTTTTTTT]TTTTTTTTTTTTTTT | 10533 |
| rs376408697 | snp | C/G | 3.29549e-05 | 0.00405911 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342207 | TACTTTAGACTTGGA[C/G]AAGGTTGTGTCTGTC | 10533 |
| rs376436342 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11457605 | AGGGGGAAACATTTC[C/T]GGAACATACATTAAG | 10533 |
| rs376436804 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11436971 | GGTGATGAAATGTTC[G/T]AATCTTAGATAGTGA | 10533 |
| rs376449503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509180 | AATAAGCAATTATGA[C/T]GCAGCGCCACATGGC | 10533 |
| rs376449694 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433249 | TGATTGTGCCACTGT[A/C]CTCCAGCCTGGGTGA | 10533 |
| rs376450479 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394974 | CAGAGATTCTAGATA[C/T]TGTACTTATTAGACA | 10533 |
| rs376453707 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516593 | CCGAATTAGTTGATA[A/G]TAGGTCCACACAAAA | 10533 |
| rs376454929 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412667 | TTTGGCAATTAAGTG[A/T]CTCTTAAGATTACAT | 10533 |
| rs376458776 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11484503 | ATTTAGGACAAAATT[A/G]GCACATCTAGCAGAT | 10533 |
| rs376459821 | snp | A/G | 0.00031524 | 0.0125507 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358589 | CGGTGGCTTCCTGCC[A/G]TCATTGCTGCAAGCA | 10533 |
| rs376487225 | in-del | -/GTCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530430 | TGTAGCTTCCAGACT[-/GTCT]TTCATCAGTTTTGAG | 10533 |
| rs376495318 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312416 | GAACAGTGTCAAAGA[C/T]AGCCTCACAAATCCT | 10533 |
| rs376531820 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11335936 | ACCCCTAATCTCATG[A/T]TCCACCCGCCTCGGC | 10533 |
| rs376532219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375923 | AAATGTTAAACAGTC[A/G]TCATATGACCCAGTA | 10533 |
| rs376536808 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336538 | ACTTTATGGTAAATA[C/T]AACTTCATAAAGAAT | 10533 |
| rs376547183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298040 | AAAAATTAGCTGGGC[A/G]TGGTGGCATGCGCCT | 10533 |
| rs376573664 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11544533 | GAAGGGGAATGAGGG[C/T]GTCAGTGGCCTGGGA | 10533 |
| rs376573903 | in-del | -/A/AA | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11451785 | TATGTTTATAGTCTC[-/A/AA]AAAAAAAAAAAAAAC | 10533 |
| rs376585891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11536578 | GATGTTTGTGTTCCA[C/T]GGAGGTCGCCACCCA | 10533 |
| rs376641595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11498326 | CTATCTGGGATGATA[C/T]TTTTGGCAGCTTTGC | 10533 |
| rs376643856 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489146 | GGAGGGTGTATGTGT[C/T]GAGGAATTTATCCAT | 10533 |
| rs376648279 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11393696 | GTAGGTTTTTTTTTT[C/T]TTTTATCTCAGTCTC | 10533 |
| rs376661099 | snp | A/G | 5.03259e-05 | 0.00501601 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315364 | AGCACTAGAGTGTGC[A/G]TATGATAATCTTTGT | 10533 |
| rs376667049 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417806 | ATTATTATTATTTTA[-/TT]TTATTTTATTTTTTT | 10533 |
| rs376690340 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313632 | TTTGAGACTGGGTCT[C/T]ACCCCCATTACGCAG | 10533 |
| rs376695158 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11487854 | TCTCAGACGGGGCAG[-/C]CTGCCGGGCGGAGGG | 10533 |
| rs376705925 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496836 | CATAGGCCTTTCCTT[-/AT]GTCATGTCTTTTTAT | 10533 |
| rs376706223 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440345 | TTTTTTTTTTTTTGA[G/T]ACGGAGTCTCGCTCT | 10533 |
| rs376737025 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304691 | CTGAATGAAGTGAAG[C/G]CCAAGTGTCTAGCTG | 10533 |
| rs376742909 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11341072 | CCCCCGCCCCGTCCC[A/C]CACCCCGCCCCAGAC | 10533 |
| rs376744180 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11454030 | CCTCAATCTTGCTAA[A/G]CTGAGCTTTTCTTTT | 10533 |
| rs376749079 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531945 | TGTGCCAAGCACTGC[A/G]CTAAACACTTTGTTG | 10533 |
| rs376761908 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11521754 | AGACGGGGTTTCACT[A/G/T]TGTTAGCCAGGATGG | 10533 |
| rs376763357 | snp | A/G | 0.405255 | 0.195948 | intron-variant | ATG7 | GRCh38.p7 | 3:11487767 | AGCTCCCTCCCGGAC[A/G]GGGTGGCTGCCGGGC | 10533 |
| rs376770452 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277410 | GGGAACCTGCCCCCA[A/G]TATTTCAAGGTATGT | 10533 |
| rs376771896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11434168 | CTCCCCCACACAGCT[G/T]GTTTTGATTTGGTTC | 10533 |
| rs376772668 | in-del | -/GAT | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11470637 | CATTCCCATTTTACA[-/GAT]GGGGAAGTTGAGGCT | 10533 |
| rs376775461 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472426 | AGTGACCCTGTCACT[-/AT]GGTAGAGGAAGGGGG | 10533 |
| rs376781271 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469461 | CTCAAAAAAAAAAAA[-/A]GTAAAATAAAATCAT | 10533 |
| rs376787960 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468447 | GACTTTTATTTACTT[A/G]CCACCTTGGAAGTCA | 10533 |
| rs376792597 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424874 | AATACTATCTATACA[C/T]AGTCTAGATATTGCT | 10533 |
| rs376799727 | in-del | -/AA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474617 | CATCTCAAAAAAAGA[-/AA]GAAAGAAAACAGAGT | 10533 |
| rs376802458 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429217 | CCACAAGTTTTAGGC[A/G]GGGCGTGGTGGCTCA | 10533 |
| rs376820829 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11355576 | GGTACTTAATTTATG[A/G]TGAAGATCTATGAAT | 10533 |
| rs376836221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11471353 | ATAGAGGCTACTTGG[A/G]TTCTGCCCCACACCT | 10533 |
| rs376849787 | in-del | -/AGC | 0.0444908 | 0.142359 | intron-variant | ATG7 | GRCh38.p7 | 3:11397739 | GGGATTACAGGCGTG[-/AGC]CACCCACGCCCAGCC | 10533 |
| rs376850028 | snp | C/T | 1.65348e-05 | 0.00287526 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298657 | CATGGATATGTTATT[C/T]TGCTGTGTTCTGTTT | 10533 |
| rs376869783 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489861 | TTGTTATAATTTCTG[A/T]TCTTTTACATTTGCT | 10533 |
| rs376872034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300917 | GTCTGGCAGGTTAGA[C/T]GTATTAAATAGAGTT | 10533 |
| rs376879684 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11407535 | GGCTCTCACCCCACA[A/T]TTTCCTTCCACACTG | 10533 |
| rs376889147 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372318 | TACAATTTTTTTTTT[-/T]CTAGACGTTTCTATG | 10533 |
| rs376893228 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368821 | CATTCCTGCTTTATC[A/C]CACTTGTGGACCAAG | 10533 |
| rs376918738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452116 | GAGCCAGGTGTGGTG[A/C]CTCACATCTGTAATC | 10533 |
| rs376924763 | snp | G/T | 1.68769e-05 | 0.00290485 | intron-variant | ATG7 | GRCh38.p7 | 3:11333117 | CCGGTCTTTGAAAAT[G/T]CATATAATTATCATT | 10533 |
| rs376974212 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422523 | GGGCTTTGCCTTAAG[C/G]GGATATTGTGGCTGG | 10533 |
| rs376991071 | in-del | -/GCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448371 | TCTCTGGCTGCTTCT[-/GCT]CACCCAGGGTGGACT | 10533 |
| rs376992218 | in-del | -/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11397742 | GATTACAGGCGTGCA[-/C]CCACGCCCAGCCCGG | 10533 |
| rs376999949 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488436 | CGGCGGTCGGGCAGC[A/G]GCGGCTGCGGTCGGT | 10533 |
| rs377024939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314047 | CTTCATTTTCAATGT[G/T]GGGAAACATAAGGCA | 10533 |
| rs377027995 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366407 | GTGGCATTTTTTTTT[-/T]GACATGCATGTGTTA | 10533 |
| rs377039448 | snp | C/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271183 | TGCTATTGCACGGTT[C/T]CTTCTCTCCCACCTC | 10533 |
| rs377052937 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410952 | GCTGGATTCTTTTGG[A/G]TATATATCCAGAATT | 10533 |
| rs377056082 | snp | A/G | 1.68134e-05 | 0.00289938 | intron-variant | ATG7 | GRCh38.p7 | 3:11313288 | TCTAATAACTTATTT[A/G]TACTTTTTTTTCTAG | 10533 |
| rs377067652 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372038 | TGCATGCTGTCTGCC[A/G]TGTTTTCATTCCCCA | 10533 |
| rs377080362 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11393300 | GGAAATCCTCTAGTA[C/T]AGATTTCAAAGCTGT | 10533 |
| rs377087790 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455040 | AGCTTTATTTCTCTC[A/G]AGTACAGTTATTTAC | 10533 |
| rs377096463 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11351116 | CCTTCCCACTGTTTA[G/T]TTGTTTAGTTGCTCT | 10533 |
| rs377114860 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369094 | TCTCTAGCCATATCT[C/T]GGGATATTTGGCCTT | 10533 |
| rs377119166 | snp | C/G | 3.29533e-05 | 0.00405901 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306971 | CCAGCCCGTTGCTGC[C/G]CAGCTATTGGAACAC | 10533 |
| rs377119973 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423399 | AATGTGACAGAGACA[C/T]GAAGTGAGCACATGG | 10533 |
| rs377135576 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479196 | AATAACAGTTTGGCA[C/T]ATAGTAAATAAAACA | 10533 |
| rs377142549 | snp | A/G | 3.43236e-05 | 0.00414254 | intron-variant | ATG7 | GRCh38.p7 | 3:11333141 | TATCATTTATCAGAA[A/G]CGGAACCAGGTTTAC | 10533 |
| rs377144611 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517188 | AAAATTATGGAGGCA[A/G]AAATTAGTTGGGGAT | 10533 |
| rs377146155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465289 | ATCTCTACTAAAAAT[A/T]CAAAAATTAGCTGTG | 10533 |
| rs377156364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551161 | CGTTTCTGTACTCGT[C/G]GTGTCCTGCGGGCCG | 10533 |
| rs377169172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11305953 | TGTCTGCATTAGCTG[C/T]GACAACATTAGTAGG | 10533 |
| rs377194823 | in-del | -/AT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278148 | ATTGTTTAAACACAC[-/AT]GTTTTACAATCAATT | 10533 |
| rs377197135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505668 | CACCACAGGAAATGG[A/G]AACCTTGCCAAGAAT | 10533 |
| rs377200133 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528471 | ACAGAGAAAAATGCT[A/T]ACCTCTGATATCACA | 10533 |
| rs377203710 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481872 | GGAGTGAAGGCCAAA[G/T]GCCTTTGGCCTGGCA | 10533 |
| rs377240717 | snp | A/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271432 | TTCACCGTTTTAGCC[A/G]GGATGGTCTCGATCT | 10533 |
| rs377244122 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465087 | ATCTCTAAAAACCTA[A/G]AGTGTGTGTGTGTGT | 10533 |
| rs377276138 | snp | A/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11299413 | AGTTCAGTGCTTTTG[A/T]CATGTGAGTATTTAT | 10533 |
| rs377298742 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11282075 | GGCAACACTGTTGAT[C/G]AGTGGAGGTAACAAA | 10533 |
| rs377320474 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359653 | GTGAACCGAGATCAC[A/G]CCATTGCATTCCAGC | 10533 |
| rs377343209 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422398 | GGAGACAGCTTCTTT[C/T]CTTAAACCTCATTAG | 10533 |
| rs377362937 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11301077 | ACAGAACTAGCGAAG[G/T]ACACAGGGGTTGTCA | 10533 |
| rs377378336 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11377038 | GCCACCGCGCCCGGC[C/G]TTGTCTGCCGCCTTT | 10533 |
| rs377379908 | in-del | -/GTTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378727 | CTGTAGGCATGTTTT[-/GTTTT]TCCAGGTTTGATTTT | 10533 |
| rs377386147 | snp | C/T | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450558 | TTGTCTACCATTCTC[C/T]ATAAGTACATGGGAG | 10533 |
| rs377386694 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366917 | GGTTGTTGGCCATCT[C/G]TTCATTTGCCCTTTT | 10533 |
| rs377437148 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11276896 | GAGTGCTACCCTCAA[A/G]CTCAAACAAGTCTAA | 10533 |
| rs377439897 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11442565 | TATTAGACTGTCAAA[A/G]TGATTAGCAATAGGT | 10533 |
| rs377450084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348213 | AAAAAAACACAACCA[C/G]GTCAGGCATGGTGGC | 10533 |
| rs377450426 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11426886 | TCTTAGAAGACTTGA[A/C]TGGTCTTACATTGCT | 10533 |
| rs377458014 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488259 | GGCGGCCGGGCAGAG[C/G]CTGCAATCTCGGCAC | 10533 |
| rs377460464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518348 | TCAAAGAGATCGAGA[C/T]CAGCTTGGCCAACAA | 10533 |
| rs377466884 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489940 | GTGTGGTGCTGAAAA[A/G]AATGTATATTCTATT | 10533 |
| rs377473547 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500111 | TTGGCTTAGATGACC[C/T]TTTAATTCCCTTCCA | 10533 |
| rs377479056 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11305945 | AGGCATTCTGTCTGC[A/G]TTAGCTGCGACAACA | 10533 |
| rs377486228 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325472 | AGGTCCGGAGTTCGT[A/G]ACCAGCCTGACCAAC | 10533 |
| rs377489365 | snp | G/T | | | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272527 | CCAGGGAGGGCGAGG[G/T]TCACAGCAAGTCTCA | 10533 |
| rs377497284 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381679 | GGTGATCATTTTGAG[A/G]GTCCTGCTTTACATA | 10533 |
| rs377497719 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11324492 | TTATGCCTCATATGG[A/G]TAGGAAAGTTACCTT | 10533 |
| rs377506754 | snp | A/G | | | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11360591 | TGCAGCTGGTCATCA[A/G]TGCTGCTTTGGGATT | 10533 |
| rs377537107 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534604 | GCATACTGCGGTTTC[A/G]TAGTCGCTGTGCTAA | 10533 |
| rs377548566 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11336379 | GTACATTTCCATTTG[-/AA]AAAGGTTTTCTGTCG | 10533 |
| rs377559573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11468391 | CCTGGATCATGCCTC[A/G]CCTATCCTCCTCCCC | 10533 |
| rs377564180 | snp | A/T | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342271 | TGCAATGTAGCTAGG[A/T]CGTTGATGGTAAGTC | 10533 |
| rs377569842 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486298 | ATTTTATTCTCTTTG[A/T]AGCAATTGTGAATGG | 10533 |
| rs377575769 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11523544 | AAGTCTGTGCTGCCA[-/T]TCCTCAGGGAGTCCT | 10533 |
| rs377581432 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540482 | ATCTCTATAAAAAAT[-/A]AAAAATAAATTCACT | 10533 |
| rs377609395 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11483637 | CATATTCAAATCCTT[A/G]TATATAGAAGTGGAG | 10533 |
| rs377661229 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330086 | ATGGGTTTTTGGAAA[A/G]AATACCACTGAGTGA | 10533 |
| rs377672571 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365579 | CCCATCAGTGAAATC[A/G]TGATGGTGCCCACCA | 10533 |
| rs377680301 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397740 | GGGATTACAGGCGTG[A/C]ACCCACGCCCAGCCC | 10533 |
| rs377716439 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495699 | AGCTGTAAGTCAGTC[A/T]TGACTGATGGCCATC | 10533 |
| rs386395939 | in-del | -/TGTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372861 | TGTGCGTGTGTGTGT[-/TGTG]GTGAAATCGGCCATG | 10533 |
| rs386395940 | in-del | -/AAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392471 | ATTAAAAAAACAAAC[-/AAAA]AAAAAAAACAAAACA | 10533 |
| rs386395942 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406001 | TGTTTTTGTTTTTGT[-/TT]TTTTTGTAGATGGAA | 10533 |
| rs386395944 | in-del | -/TTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471759 | CTTTTTTTTTTTTTT[-/TTT]TTGAAATGTAGTCTC | 10533 |
| rs386395945 | in-del | -/ACAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478996 | TATTTACAACACACA[-/ACAA]CACACACACACACAC | 10533 |
| rs386395946 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500454 | TATGCAATACAACTA[-/A]AAAAATACAAATTAA | 10533 |
| rs386395947 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500459 | AATACAACTAAAAAA[-/A]TACAAATTAAAAGAC | 10533 |
| rs386658446 | multinucleotide-polymorphism | AT/CC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278460 | CCCTCCGTTCAGGGT[AT/CC]GTGACTTCCCGCAAC | 10533 |
| rs386658447 | in-del | AGGA/CTTACT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306115 | ACTTTGCTTACTCTG[AGGA/CTTACT]CTGTGAGGCCTTTGG | 10533 |
| rs386658448 | multinucleotide-polymorphism | AA/GT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330197 | TTTCTCCACTGTAAA[AA/GT]TACTATTTTTTCTTT | 10533 |
| rs386658450 | in-del | AT/TTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382061 | GGCTAAAAATTACTT[AT/TTA]AAAATTTATCCTTTG | 10533 |
| rs386658452 | multinucleotide-polymorphism | AGCTACTTCAGGGGGT/CGCTACTTCAGGGGGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396324 | CATGCCTGTAGTTCC[lengthTooLong]TGAGGTGAGAGGATT | 10533 |
| rs386658453 | in-del | GG/TTTGGGCTATCATGAATAGCGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426044 | TCAATGGTTTCTAGT[GG/TTTGGGCTATCATGAATAGCGC]TGCTGTGGACACTTT | 10533 |
| rs386658455 | in-del | C/TGGGG | | | intron-variant, frameshift-variant | ATG7 | GRCh38.p7 | 3:11434353 | GGAGAGAAATCGCTC[C/TGGGG]ACTGAACTAGCCTGC | 10533 |
| rs386658456 | in-del | A/GAAT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441367 | CTACCTCAACCTCCC[A/GAAT]AGCTGGGATTACAGG | 10533 |
| rs386658457 | in-del | AT/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445056 | AAAGTCAAACAATAG[AT/G]GCTGGCGAGGTTGTG | 10533 |
| rs386658458 | multinucleotide-polymorphism | CA/TG | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447165 | TTGAACTCTTTTTAG[CA/TG]TAAAAGAGTAATTTA | 10533 |
| rs386658459 | in-del | C/GGGGGGTTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452016 | GGTCACCAGGGACTT[C/GGGGGGTTG]GGGGGTTGTGGGAGG | 10533 |
| rs386658460 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458614 | AACACATTGTGTGAC[CA/TG]TAGCTAGTTACTTCT | 10533 |
| rs386658461 | multinucleotide-polymorphism | AGA/GGG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466317 | TTTTGGACCCCATAC[AGA/GGG]TAAGGTGAGAAAATT | 10533 |
| rs386658462 | in-del | AG/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471250 | CCTACCGCTGGCCCC[AG/C]CTTCCTCTCAAGCTG | 10533 |
| rs386658464 | in-del | AA/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506040 | TGGGAATGCTTTGTA[AA/G]TAGAACATTTCTGTA | 10533 |
| rs386658465 | multinucleotide-polymorphism | CG/GA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532822 | TACTGCATGAGATGT[CG/GA]TTAGCATGGTGCCTG | 10533 |
| rs386658466 | in-del | ACA/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535463 | GTTTGTATGGCAATC[ACA/G]GGGGCCAGGCAGGTC | 10533 |
| rs386658467 | multinucleotide-polymorphism | AGT/GGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539819 | GAACCAGCACAGTTC[AGT/GGC]GACATCGAGCAGGTC | 10533 |
| rs386658468 | multinucleotide-polymorphism | CGC/TGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551787 | AGGGTCTCACCCTGT[CGC/TGA]CCAGGCTGGAGTATA | 10533 |
| rs397688781 | in-del | -/TG | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11321425 | TCAGTTTTGACCGTG[-/TG]ACCAGCATGCAGCTG | 10533 |
| rs397688889 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11418909 | GGAAGTGCCACTTTT[-/T]AAATCATCAGATCTC | 10533 |
| rs397700322 | in-del | -/GT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465114 | TGTGTGTGTGTGTGT[-/GT]AAGGACACCTCCAGA | 10533 |
| rs397703827 | in-del | -/A | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11414001 | ATCTAGGTTATGGTA[-/A]TTAGGTTTGTAATTT | 10533 |
| rs397734095 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11294396 | GGCTAATTTTTTTTT[-/T]ATTTTTAGTAGAGAT | 10533 |
| rs397744147 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11428403 | TCCCTGGTGTACCTG[-/A]AAAATCTCACAATCT | 10533 |
| rs397747500 | in-del | -/TT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11406006 | TTGTTTTTGTTTTTT[-/TT]GTAGATGGAATCTCA | 10533 |
| rs397753624 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465059 | GGAAAAATTTTTTTT[-/T]CTTATCAAATCAATC | 10533 |
| rs397758474 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11411988 | GTCCTTTTTTTTTTT[-/T]ACTGAAACACCAGGG | 10533 |
| rs397758562 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326296 | TGCTGTTTTTTTTTT[-/T]GTTGTTGTTGTTTTG | 10533 |
| rs397761178 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11424983 | ATATCCCTTTTTTTT[-/T]GTTTTTGAAGACTCT | 10533 |
| rs397767101 | in-del | -/GAG | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11463626 | TTATCATAGGTGGAG[-/GAG]AGTGTTGGAGCATTG | 10533 |
| rs397776268 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451973 | GTTCAGAATAGACAA[-/A]TCCATAGAAACATAA | 10533 |
| rs397777517 | in-del | -/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11349242 | GTTGAGTGGGGACTT[-/G]GGAGAACTTTTCTGT | 10533 |
| rs397795601 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11309463 | TGTCTTTAAAAAAAC[-/A]AAAAAAAAAAAATCA | 10533 |
| rs397796000 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11444874 | TTTACAAGGAAAAAA[-/A]CCCCATTAAAAAGTG | 10533 |
| rs397797049 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11476433 | TTTTTTTTTTTTTTT[-/T]GGTTTTTCCTTAGAT | 10533 |
| rs397799138 | in-del | -/C | 0.375 | 0.216506 | intron-variant | ATG7 | GRCh38.p7 | 3:11522479 | CAGTATGAGGCTCAT[-/C]CGCTCATCTCACTAA | 10533 |
| rs397804666 | in-del | -/T | 0 | 0 | intron-variant, frameshift-variant | ATG7 | GRCh38.p7 | 3:11450199 | ACATGGAACCTAAGT[-/T]GTTCAAGGTCATGGA | 10533 |
| rs397809050 | in-del | -/ATAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11540487 | TATAAAAAATAAAAA[-/ATAAAAA]TAAATTCACTGGGCA | 10533 |
| rs397809131 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438598 | ATAAAGATTTTTTTT[-/T]CTTTTTAACCTAAAT | 10533 |
| rs397818463 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332195 | ATGAAATGTCATATA[-/A]CAATGAATCTGAGTG | 10533 |
| rs397831750 | in-del | -/TGTC | 0.264164 | 0.249598 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557339 | ATATCACAGATTGTC[-/TGTC]AGTAATCTGCTGTTC | 10533 |
| rs397840025 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533221 | AGCTGCTGACCCCCA[-/A]GCCCTCCTCTCCAGC | 10533 |
| rs397876378 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11516032 | CTCACATTCCTTTTT[-/A]AAAAAAAAAAAAAAC | 10533 |
| rs397876491 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404127 | TTAACCAGCTCAATT[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs397877076 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404127 | ATTAACCAGCTCAAT[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs397938088 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339313 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 10533 |
| rs397945737 | in-del | -/CA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451901 | ACACACACACACACA[-/CA]GACACACACACACAC | 10533 |
| rs397954526 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409789 | CTTTTTTTTTTTTTT[-/T]CCATGTGGTTGTCCA | 10533 |
| rs397959434 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495461 | CTGGCAGAGACCCCC[-/C]AGACATCTTGATAAT | 10533 |
| rs397966587 | in-del | -/A | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556640 | GAACAACAAAAAAAA[-/A]TGAATGATTACAATA | 10533 |
| rs397977670 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524814 | AAAAACAAAAAAAAA[-/A]CAAAACAGGCATTCT | 10533 |
| rs397988683 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11285159 | AAAGGCCGGGCTTTT[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs397988684 | in-del | -/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11314781 | TCAGCTAACTTTTTT[-/G]GTATTTTTTATAGCG | 10533 |
| rs397988685 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11322231 | TTTGCAAAAGTCTTG[-/T]TTTGTTATGTGTATG | 10533 |
| rs397988686 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11368752 | CGTCACCTTGATTCC[-/T]TTTTTTTTTTTTTTG | 10533 |
| rs397988688 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11381310 | CTCAACCATTCAAAG[-/A]AAAAAAAAAATCTGC | 10533 |
| rs397988689 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11432465 | TCCATTATATCATTC[-/T]TTATGCAAGGCTCCT | 10533 |
| rs397988690 | in-del | -/A | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11439086 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs397988691 | in-del | -/A | 0 | 0 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451230 | AGTGATATAGATCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs397988692 | in-del | -/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11467152 | TTAAGAAGCCATCAG[-/T]TTTTTTTGTTTGTTT | 10533 |
| rs397988694 | in-del | -/CT/TT | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11533556 | TATTTGTGTAATGGC[-/CT/TT]TTTTTTTTTTTTTTT | 10533 |
| rs398051574 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11299942 | CTTTTTTTTTTTTTT[-/T]GAGACAGGATCTCAC | 10533 |
| rs398051575 | in-del | -/T | 0.5 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11342947 | AATTTTTTTTTTTTT[-/T]GAGACAAAGTCTCAC | 10533 |
| rs398062093 | in-del | -/AAAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470003 | CAAAAAAAAAAAAAA[-/AAAAAAA]GAGAGAGAGAGATGG | 10533 |
| rs398081890 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326295 | ATGCTGTTTTTTTTT[-/T]TGTTGTTGTTGTTTT | 10533 |
| rs398081891 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336206 | ACATGGCTATTTTTT[-/T]TGTATTTTAGTAGAG | 10533 |
| rs398081892 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390684 | TTGATTTTTTTTTTT[-/T]TCCAGAAAGTAATTT | 10533 |
| rs398081893 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11428402 | CAGATTGTGAGATTT[-/T]TCAGGTACACCAGGG | 10533 |
| rs398081894 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467151 | AAAACAAACAAAAAA[-/A]ACTGATGGCTTCTTA | 10533 |
| rs398091290 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397780 | TGATTTATAATCACA[-/A]GTAGAAAATTTTAAT | 10533 |
| rs398105598 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11393695 | GTAGGTTTTTTTTTT[-/T]CTTTTATCTCAGTCT | 10533 |
| rs398105600 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468314 | AGGGGTAAGTGGAGC[-/C]TAGTGGGAGAGCACA | 10533 |
| rs527247234 | in-del | -/TTTATTTA | 0.00882063 | 0.0658218 | intron-variant | ATG7 | GRCh38.p7 | 3:11525032 | CTGTGCAAATCTCAC[-/TTTATTTA]TTTATTTATTTATTT | 10533 |
| rs527251057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542538 | ACCTTGCCATGGGCC[A/G]TGGCCCTTCCTGTGG | 10533 |
| rs527251113 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444431 | GAGAGCCACTAAACA[C/G]TGTCATATCTAAGAT | 10533 |
| rs527251971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330093 | TTTGGAAAAAATACC[A/G]CTGAGTGAAGTACCC | 10533 |
| rs527262268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11463517 | ATGTCAGCCCTTCCC[A/G]CATTTAGACTTGGTT | 10533 |
| rs527263693 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277902 | TAGACCCCCCCCCCC[-/G]CCACCAGGAATGCAT | 10533 |
| rs527265669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456590 | AAACCCATGGTGTTT[C/T]GCTTAACACTAATAC | 10533 |
| rs527274849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499827 | CAGGGCACCTCCACA[C/T]GCAGTTTGGGAGCCA | 10533 |
| rs527282409 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11372247 | TGATTCCCAGGTGGG[-/T]TTTTTTAATATTCAG | 10533 |
| rs527287154 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11405864 | GGCTTAAGACATCCA[C/G]CGCCTTGGCCTCCCA | 10533 |
| rs527292007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323622 | CTACTTCATTCAGAG[C/T]AGTTATTGAAGATTG | 10533 |
| rs527312692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364829 | CCAGCCCACTTCATA[C/T]CCACCCTACTTACCC | 10533 |
| rs527331515 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419135 | TTTTAAGTCATCAAG[A/G]GCAAGTAAGTATAAT | 10533 |
| rs527331521 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11390428 | TGCTATTTTTGATAA[-/TAT]TCCAATAGGCGCTGA | 10533 |
| rs527347927 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11377783 | CACTGTGAGTATTCT[C/G]AAGCCTGTAACTTCC | 10533 |
| rs527385600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499114 | AATTTAGTAGCCACT[G/T]GAAAAACTGCACATA | 10533 |
| rs527391826 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11335833 | CTCCCGAGTGGCTGG[A/G]ATTACAGTCGCGTGC | 10533 |
| rs527402718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11441893 | CTGGTCTTGAACTCT[C/T]GACCTCAGGTGATCC | 10533 |
| rs527402728 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11410992 | GATCTAATAATTCTC[-/TT]TTAATTTTTTTAAGT | 10533 |
| rs527417748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286051 | TTTCAACTTGGGTTT[A/T]TCTGATGTTTCCTCC | 10533 |
| rs527429450 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | ATG7 | GRCh38.p7 | 3:11506041 | GGGAATGCTTTGTAA[A/G]TAGAACATTTCTGTA | 10533 |
| rs527438128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483244 | CCCATCCTCTCTGGT[C/T]AGTCTTGGCATCACA | 10533 |
| rs527448798 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400342 | TCCCTCTTATGCTGA[C/G]TACCCAGATAATAGG | 10533 |
| rs527451887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524177 | GCCCCTTTCCTCTGA[C/T]TGTCTACCTGGCAGG | 10533 |
| rs527453438 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11395892 | TCGCAGTGAGCGGAG[A/G]TCACACCACTATACT | 10533 |
| rs527456277 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363259 | TTTTTTTTTTTTTAA[C/T]GAGACGGAATTTCGC | 10533 |
| rs527476113 | in-del | -/GAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517367 | GAAAAGAAAAGAAAA[-/GAAAA]AAACAATGATGGAGA | 10533 |
| rs527479502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11309452 | AAAATCGCTTGTTGA[C/T]TTTTTTTTTTTGTTT | 10533 |
| rs527481621 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11397756 | ACCCACGCCCAGCCC[A/G]GAAATAAATGATTTA | 10533 |
| rs527490382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368527 | CTAGGCACAGTGGCT[A/C]ACCCCTGTAATCCCA | 10533 |
| rs527491476 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331902 | TACTACATATCCACC[A/G]AAAGTATTTAATAAA | 10533 |
| rs527501939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525007 | AATTTAAGGGTATTT[A/G]TTCCTCTGTCTGTGC | 10533 |
| rs527502860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310040 | GTGTGGTGGCGCCTG[C/T]CTGTGGTTCCAGCTA | 10533 |
| rs527510699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11445448 | AGAAAACCTAATACC[A/G]TATGTTATCACTTAT | 10533 |
| rs527512642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303077 | CCTGAGGACTTTGCA[C/T]TGTGTGCTGATTAAG | 10533 |
| rs527514901 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495080 | AAGGCTCCGTCTCAG[-/A]AAAAAAAAAGGCTTG | 10533 |
| rs527534569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350630 | ACAGTGGTACAGTGC[A/C]ATGTCTTCCATTTCT | 10533 |
| rs527544721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451174 | TGAAAAGGACAGGCT[A/G]GAACAAGAACTTGAT | 10533 |
| rs527562567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530981 | GTGATACTCTATCTC[A/G]GAAAATAATAATAAT | 10533 |
| rs527562674 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11393346 | AATAGCCACACCTGG[G/T]GTATGCACTCCTGAT | 10533 |
| rs527594334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357807 | TTGAGCCAAGGAGTT[C/T]GAGAGCAGCCTGGGC | 10533 |
| rs527596729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444928 | TCTAAAAGAAGACAT[A/G]CATGTGGCGAAAAAG | 10533 |
| rs527617857 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408420 | CTCCAAACTGTTCCA[A/G]CCTCTGCCTGTTACC | 10533 |
| rs527639912 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11504276 | AGGGAAATTATATCT[A/G]ATCTACAAGTCTGTA | 10533 |
| rs527653144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432115 | CATAGTGGAGACTGG[C/G]GACCAGGCTGACAAA | 10533 |
| rs527655400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424523 | AACAAAAGTTAGAAA[C/G]CACTACCCTTTAACA | 10533 |
| rs527675470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470650 | CAGATGGGGAAGTTG[A/G]GGCTCAGAGGTGTGT | 10533 |
| rs527679846 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11295828 | TTTCGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 10533 |
| rs527684651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385234 | GGGGTTTCACCATGT[C/T]GGCCAGGTTGGTCTC | 10533 |
| rs527694478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11471274 | TCAAGCTGGCCCTGG[A/C]GCTCTGGACTCCTCA | 10533 |
| rs527701028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385901 | TTGTCTTTGTGAGTG[C/T]CGTTTTAATTTTGGC | 10533 |
| rs527706563 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308732 | GCCTGGTTGCCCCCT[C/T]GGTGCTGAGATCTGC | 10533 |
| rs527706873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512652 | GGCTTCAGGAGTGAA[A/G]CTGCAGACCTTCACG | 10533 |
| rs527709232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507174 | GTAGTGCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 10533 |
| rs527716866 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448550 | TAAAACCAAATCTGT[A/C]ATCAGGAACATAAAC | 10533 |
| rs527719853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379260 | CATATTTTTATGATA[A/T]ATAGAACAGCTTAAA | 10533 |
| rs527725053 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11482291 | TGGTGTTTGGGCTCC[A/G]AGCTCTTTCAAGAAA | 10533 |
| rs527741985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303735 | GAATGAAGAACATTT[C/T]TGTGGGTTTCTTTCC | 10533 |
| rs527751921 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523415 | GGCCTAGACAGAAGA[A/G]ACAGGGAGGATTATT | 10533 |
| rs527762889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343016 | CTCACTGCAACCTCC[A/G]CCTCCTGAGTTCAGC | 10533 |
| rs527765172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351179 | AGACCTCCCGTGTTC[C/T]AGGGACAGGGGAACT | 10533 |
| rs527768895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11439363 | TGTGAGCCACTGCAC[C/T]GGGCCTGAGCTCTTA | 10533 |
| rs527784230 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303676 | CCGTCTCTAAAAAAA[A/T]AAAAAGAATTTTCCT | 10533 |
| rs527799780 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554960 | CTCCTCCATACCCCG[A/G]GGTCTGGGATTCCCC | 10533 |
| rs527810441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477934 | TTCTTAGCTTAACTC[C/T]AGTGGAAAGCAGTCT | 10533 |
| rs527817049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11519459 | CTTTCTTTCTCAGTG[C/T]GGAGGGGTAAATTGG | 10533 |
| rs527819729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306093 | CAACTCCTCTTCTCT[C/T]CTCCTGACTTTGCTT | 10533 |
| rs527831596 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286492 | TTTGGGTTATTTCTT[A/G]CTTTTGTTTCTTTTC | 10533 |
| rs527838965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11538295 | GCCAGCACAGACTCT[A/G]TCACACCATGGACCT | 10533 |
| rs527844170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274135 | GAAATCCTTTAAGAG[C/G]TGAGTACTGGACTTT | 10533 |
| rs527865890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458373 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCT | 10533 |
| rs527868699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501851 | TGCGCCACCACATCC[A/G]GCTAATTTTTGCATT | 10533 |
| rs527873758 | in-del | -/AGAG | 0.00653588 | 0.056791 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557869 | AAGCACCTGAAATCT[-/AGAG]AGAGAAAGACCTATA | 10533 |
| rs527894297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317744 | ACTACAGGTGCGCAC[A/C]ATCATGCCCAGCTAA | 10533 |
| rs527895265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405136 | TCTGATAGTTTTCAA[C/T]AGTTGGCCCTGGAAA | 10533 |
| rs527916195 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11390457 | CTGAAAGTATACCTG[G/T]AAAATGAGACCTATG | 10533 |
| rs527929692 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11452289 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 10533 |
| rs527930339 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426746 | TTAGAAGTGAAAGTC[-/TT]TTAATTTGCATTTTA | 10533 |
| rs527935297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532698 | ACTGCACTCCAGTCT[A/G]GGTGACAGAGTGAGA | 10533 |
| rs527946492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507644 | TGTTTTTTGTTTTTG[A/T]TTTTGTTTTTGTTTG | 10533 |
| rs527948090 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11275767 | TTAATTGGTAGTCAG[A/T]AGGTATTACCATGAT | 10533 |
| rs527952246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465145 | GAGTTCTAGAGCTGA[G/T]TGAAAACCTGGTTTA | 10533 |
| rs527973623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330504 | GGCATGCCCCAATTC[A/G]TTTGTTTTTTGAGTA | 10533 |
| rs527973813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11273101 | TGCGTGCAGTTTCCT[C/G]ATTTTTAAACACTGG | 10533 |
| rs527986377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280740 | ATGGTAATAAGAATA[C/G]TTTATTGAATATGTT | 10533 |
| rs527989420 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11385631 | TCTGTCCTCTTGTTA[C/T]GGCATCCCAATACCA | 10533 |
| rs527999414 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11440262 | ACTTGCGACTCCAAT[-/C]CCAACTTACCATTGG | 10533 |
| rs528012111 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451941 | TATCTCTTAAATGAG[A/G]TTCTATTTTTGTGAA | 10533 |
| rs528024913 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331375 | TCCCTGTAACTTAGC[C/T]CAGTACCCTGGATGG | 10533 |
| rs528030099 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11428257 | GCCCCAAGTTGTCAA[A/T]GAATAGATGGCCAGG | 10533 |
| rs528030588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418443 | TGGCTTCTTTTATCT[A/C]CCTTTGCTGGAAGCA | 10533 |
| rs528043107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436085 | AAAAACAACAACAAA[A/C]CCCAGAATATATAGG | 10533 |
| rs528066750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552112 | GTTATAATTGGTTGT[C/T]GTCAATTTTATATCT | 10533 |
| rs528067894 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484445 | CGACAAACCCAAAAG[C/G]GTTAAGTCTTCAAAG | 10533 |
| rs528075287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474179 | CTGAATGCTCAGCAC[C/T]CTTCTAAGCACTGGG | 10533 |
| rs528087133 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11474762 | CGGAATGCAAAGAAA[G/T]GAGCCAGACATGTGA | 10533 |
| rs528104086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552682 | ATGCATTTTACAAAA[C/T]AATAATCCCCGCACA | 10533 |
| rs528108671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458964 | GGGATCTGGGTTGCC[C/G]GCAGCTTATGAGATT | 10533 |
| rs528110619 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11421311 | TACCCACAGCAGAAC[G/T]TCTTTAAAAATTGGA | 10533 |
| rs528111947 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286351 | CGCTAAGGTCTTAGT[C/T]CTGAAAAAACAATAA | 10533 |
| rs528113840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515604 | CAAGACATTGTCCCA[A/G]GGGTAATGACAGAAT | 10533 |
| rs528127353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306721 | AGAACAGCATCCTGA[G/T]AGGTTAGAGTATAGG | 10533 |
| rs528148153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298171 | CAGAGTGAGACTCCA[C/T]CTCAATTAAAAAAAA | 10533 |
| rs528148542 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11514964 | CCTGCCTCAGCTTCC[-/T]TGAGTAGCTGGGATT | 10533 |
| rs528150971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11354078 | GTATCCCAGACTAAC[C/T]GTATTCTGGCCCCAG | 10533 |
| rs528159769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11346219 | TTCTGATAGGATGAA[A/G]CATAACTTACTGAAC | 10533 |
| rs528167868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442226 | TGTGGGCCCAGAAAC[A/G]GGGTGGTCTTATGGA | 10533 |
| rs528177011 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557427 | AAACCCCACCTCCCC[C/T]GGGAGCTTGTAACAA | 10533 |
| rs528185307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521691 | CCGAGTAGCTGGGAT[C/T]ACAGGCGCCTGCCAC | 10533 |
| rs528188929 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11316104 | TTAATTTTTATTCCC[A/C]GAACTACCCTGTAGT | 10533 |
| rs528192232 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11435025 | CCTTTCTAGAAAAAA[A/G]TGAAATGCTTTTCAA | 10533 |
| rs528221699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480588 | AAACAGACAAAAAAA[A/C]CTTACAATCTGTGCT | 10533 |
| rs528228590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318532 | CCTTTCCTACCTGTG[A/G]CCCTGAATGTTCCTG | 10533 |
| rs528230589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277030 | AGTCATCTCAGACTC[C/T]TCCTCTGGTACTAGC | 10533 |
| rs528230711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515106 | AGCCTACCAAAGTGC[C/T]GGGATTACAGGCATG | 10533 |
| rs528233716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546889 | CCCACCCTTGCCAGC[A/G]GAGAGCAGCACAGGC | 10533 |
| rs528250744 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436785 | ACATTGAAAATGTTA[A/C]ACTAATTGAAGAAGC | 10533 |
| rs528257188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11497762 | TTTTAGTTTCCCATG[C/T]CTCTGCCAATATTCC | 10533 |
| rs528275767 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11461127 | CAAAGGGTGGGGCAG[C/G]GTTTGTGGAAGCCAT | 10533 |
| rs528292854 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11432990 | GTTCTCCCCAAGTAT[C/T]TTTTAAATTGCTGCA | 10533 |
| rs528301622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357772 | TTCCAGCACTTTGGA[A/G]GCCGAATCAGGAGGA | 10533 |
| rs528301743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370323 | AGCTTAGTTTTTCTG[C/T]CCCCTTGGTGACTCT | 10533 |
| rs528304956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320703 | CATTGTGTCTGCATC[C/T]CATGGCATCATGCCT | 10533 |
| rs528320460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11375580 | TCCCCTTGCCCCCAA[A/G]ATGGAGCCTTGCTCT | 10533 |
| rs528325367 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11360080 | GATAGAATCTTGCTC[-/T]TGTCACCCAGGCTGG | 10533 |
| rs528335307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455025 | GATTTATAAAAGTTC[A/G]GCTTTATTTCTCTCG | 10533 |
| rs528339793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535567 | TCAGGCCAGTGAACC[A/G]AGGGGACAGCTACAA | 10533 |
| rs528344630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467467 | CTGCAACCTCCGCCC[C/T]CCAGCTTCAAGCGAT | 10533 |
| rs528354466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428530 | CCACTTATGGCCAAT[A/G]GTTAGAGCCACAAAG | 10533 |
| rs528370935 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11284298 | GGGCGGTCTCACTCC[A/G]GGAAGCACTCCTGCT | 10533 |
| rs528372354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11420919 | TGCCACCTTGTCCGG[C/T]TAATTTTTTGTATTT | 10533 |
| rs528381983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276520 | TCTTGGAAGAGTTAT[C/T]TAGAGTTGCTTCCTG | 10533 |
| rs528386257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333663 | ATATATATACACATA[G/T]ATATATTTACATATG | 10533 |
| rs528397349 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433124 | TGGTGAGCCTCTGTC[A/T]CTATTTAAGAAAATT | 10533 |
| rs528402441 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11343054 | CTGCCTCAACTTCCC[A/G]AGTAGCTGGGACTAC | 10533 |
| rs528409103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546413 | CTGACCTCAGGTGAT[A/C]CGCCTGACTTGGCTT | 10533 |
| rs528409307 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461597 | TCACTCTCTCTCTTA[A/T]ATGTAGTTCTTAGAA | 10533 |
| rs528412575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334480 | AACTCCTGACCTCAA[G/T]TGATCCACCCACCTT | 10533 |
| rs528428487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11486662 | CCATTCAGTATGATA[C/T]TGGCTGTGGGTCTGT | 10533 |
| rs528437451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402260 | AACATGGTGAAACCC[A/G]GTTTCTACTAGAAAT | 10533 |
| rs528467872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396272 | GCCAACACAGTGAAA[A/C]CCCATCTTTACTAAA | 10533 |
| rs528473102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314767 | TCGTGAAACCCCATC[A/G]CTATAAAAAATACCA | 10533 |
| rs528506328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530304 | TGTGTGTGCGGTGCG[C/T]GTGCAGTCCCTGTGC | 10533 |
| rs528508019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11482101 | CTCTCTCTCCTGATG[C/T]CCCGGTTCCTTCTCT | 10533 |
| rs528514243 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11315130 | CTTTGTGCCCCTAAG[A/T]CACACACCACCATGC | 10533 |
| rs528525172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11443701 | TGAGTCACTGCACCT[A/G]GCCGAGGAGGTTTGT | 10533 |
| rs528535980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455554 | TCTTCCGGTGACATC[C/G]ATTTTTCCTAAAAGT | 10533 |
| rs528544835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492125 | TGAGACTCCGTGGTC[A/G]TAGGACCCTCCGAGC | 10533 |
| rs528547789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11449436 | GAGTCTTCACTACCC[C/T]TGGTGGCTGTACTTT | 10533 |
| rs528550067 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357794 | TCAGGAGGATTCCTT[C/G]AGCCAAGGAGTTCGA | 10533 |
| rs528550972 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270903 | ATACGTGCAGGTCAC[C/T]GGGGATATGATGGCT | 10533 |
| rs528559803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498401 | CAGCTACTCTGTATT[A/G]TCATAGGCTTTTGCT | 10533 |
| rs528578799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11363316 | GGCACGATTTTGGCT[C/T]ACTGCAACCTCTGCC | 10533 |
| rs528582090 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413279 | TCCTTCTTTCATCAC[G/T]GTGTATATTTGCTGT | 10533 |
| rs528582169 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11536037 | GGGCCTCCATCTCCA[C/T]GGGTTCTAAAGGAAA | 10533 |
| rs528591331 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304702 | GAAGGCCAAGTGTCT[A/G]GCTGTAATGTCCCCA | 10533 |
| rs528599694 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11407821 | CCTTAGGCTGTACAC[A/C]GCACAGGGACCCTGG | 10533 |
| rs528637919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321636 | TTTCTGCTCAGCTCA[C/T]AATGTGTTGGGGTAG | 10533 |
| rs528638480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390469 | CTGGAAAATGAGACC[C/T]ATGTCATCCTATCCC | 10533 |
| rs528642479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11314120 | TCTCCTACCCTTGTA[C/T]CAAGTTGCAGAACTT | 10533 |
| rs528655093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292540 | GCTAGGATTACAGGC[A/G]TGAGCCACCACACCC | 10533 |
| rs528670801 | snp | A/G | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527131 | TTTTTTTGAGGTGGA[A/G]TCTCACTCTGTTGTC | 10533 |
| rs528678660 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11281208 | AGGCTGTGCACTGCA[C/G]AAGAGGCCACATCAA | 10533 |
| rs528678993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301842 | TATCCTTATCCTTCT[A/G]CTGGACTGTTTGTTT | 10533 |
| rs528680488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298454 | AGATCTGTTTCACAA[C/T]GTTGTGATTATACTT | 10533 |
| rs528682605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511619 | CAGCCCTTGGGCGGT[C/T]GATGGGACTGGGCGC | 10533 |
| rs528689517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492187 | TTTTTAAAGCCCATC[A/G]GAAAGGCGCAGTATT | 10533 |
| rs528689813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553869 | GCCTCCCATCTCCCC[A/G]GGCCAGCCTCGTGTA | 10533 |
| rs528694179 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11383832 | CCCATACTACTACAG[A/C]AAATAAACCTAGAAC | 10533 |
| rs528713867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11548003 | TGCACCACCACACCC[A/G]ACTAGTTTTTAAATT | 10533 |
| rs528717746 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466896 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 10533 |
| rs528739644 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11324990 | TAATACTGTATTTTT[A/G]CTATACCTTCTATGT | 10533 |
| rs528763401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11515118 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC | 10533 |
| rs528775089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11437159 | CTCTGGTTCTCTCTG[C/T]ATGCAATGTTGATTT | 10533 |
| rs528777025 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325694 | AAAAAAAATTTTATC[C/T]TATAGATGAGAAAAT | 10533 |
| rs528787494 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11429718 | TTTGGGAGGCCAAGG[C/G]TGGTGGAGTGCCTGA | 10533 |
| rs528797336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349232 | CTCTAGCTAGACAGA[A/T]AAGTTCTCCCAAGTC | 10533 |
| rs528813414 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461675 | TTAACCCCCAGAAAC[A/G]GAACATCAAAACCAA | 10533 |
| rs528816633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341343 | GGGATTACAGGCATG[A/T]GCCACCACACCCAGC | 10533 |
| rs528817518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11490046 | TTGTTAACTTTCTGT[C/T]TCTTTGATCTGTCTA | 10533 |
| rs528840504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405043 | GTATTTTCCAGATTT[C/T]TTAAAGCTTTTTGTT | 10533 |
| rs528856347 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11476726 | ATCAGATGTTTTTCT[-/TC]TTTTTCATTTTTTTC | 10533 |
| rs528860552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398878 | CCTTAAAACAGGCCC[A/G]AAATTAATGAGCAAA | 10533 |
| rs528864473 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336223 | GTATTTTAGTAGAGA[A/C]GGGGTTTCACCGTGT | 10533 |
| rs528876108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11317733 | AAGCAGCTGGGACTA[C/G]AGGTGCGCACCATCA | 10533 |
| rs528884362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533235 | AAGCCCTCCTCTCCA[G/T]CTCCCTTTCATCATC | 10533 |
| rs528890650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11525755 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10533 |
| rs528899133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464199 | CAACATGGTGAAACC[C/T]CATCTCTACAAAAAA | 10533 |
| rs528904722 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293723 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10533 |
| rs528927026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446296 | AACATTCTGTGATAA[C/T]GATAGAATAAGTCTT | 10533 |
| rs528938337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493912 | TACACTTAAAACTAC[C/T]GAGGGGTATTGAGAA | 10533 |
| rs528948917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11501041 | GCGAGGATCACTTGA[A/G]GCCAGGAGTTCAAGA | 10533 |
| rs528965302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411073 | AGCAATGTAGAAGTC[C/T]TTTTTTATCGTCACA | 10533 |
| rs528967708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531975 | GGCATCATTTTATCA[A/C]ATTTCTCCCAGAATC | 10533 |
| rs528976313 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488614 | CCGACCCCAGCCCGC[A/G]GGCCTTCGAGCCTTC | 10533 |
| rs528978295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272985 | TAAATATAGGTGTTA[A/G]AACATTTGTCAGAAA | 10533 |
| rs528983197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418285 | ATTTTTTTTTTTTTT[A/T]ATATTTTGTAGAGAC | 10533 |
| rs528986398 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11366892 | TTTCAAATGTCTGAA[G/T]GATTATTTTGGTTGT | 10533 |
| rs528989375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11376400 | TATTTTGGGCATAAA[A/G]ATCAAAAGGATTTCA | 10533 |
| rs529000629 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11489227 | AAGCTGTCAGACAGG[A/G]ACATTTAAGTCTGCA | 10533 |
| rs529020070 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11290366 | GAGGAGGGGCAGGCC[A/T]GGCCAAGCATGAGGA | 10533 |
| rs529032668 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11411664 | TTCTTATCAGATATG[A/G]TTTTCAGATTATTTT | 10533 |
| rs529040343 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498621 | AACGCCTCAGCTGGT[C/G]CTCCAAGACCTGCTG | 10533 |
| rs529050849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288286 | TAAACTGCTGAAATT[C/T]ATCTTACTATATAGC | 10533 |
| rs529067414 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11305007 | TTACTCTCCATCCCC[C/G]CTCCTCCATACTCAC | 10533 |
| rs529068790 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11302759 | CCCAGTACTCACTTA[C/T]AGATGTCAAGAGTAT | 10533 |
| rs529070545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11513388 | CCTGAGCCCTGCCCC[A/G]CGGGGAGGCAGCTAA | 10533 |
| rs529081214 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365513 | CTTATTTGGAAATCA[-/T]TTTTTTTTAGATTCC | 10533 |
| rs529083492 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415860 | ACATAGTTGATTATC[A/T]AGTATTATGTACTAT | 10533 |
| rs529084956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479286 | ATTTTTTCTTTAGGT[A/G]AACTGAGTTTAAATT | 10533 |
| rs529103573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11386963 | ACATTTCTCCCTTTG[C/T]TTCTATTTCCTCATC | 10533 |
| rs529120333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433014 | TGCTGCATTTGGGAT[C/G]GGTACAGTGGCTTAC | 10533 |
| rs529125575 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11411741 | ATGAAATTCAGTCTA[-/T]TTTTTTTTGTTTCCT | 10533 |
| rs529147519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519684 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 10533 |
| rs529158810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446739 | AAATCCAGTCAAGGG[A/G]CTACTTGGGCCTGGA | 10533 |
| rs529166515 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299278 | TGGGCTCAACAAAGA[A/G]AAGAAAACTATTCAT | 10533 |
| rs529168419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439732 | AGGTGCGTCTTGAAG[A/G]TTGGAGCTCCAAGTG | 10533 |
| rs529177937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526319 | TCACTTGAGCCCAGG[A/G]AGGCCGAGGCTTTAG | 10533 |
| rs529178701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432331 | TAGGATGCAATAAAA[A/G]AAATTTTAATGAGAA | 10533 |
| rs529179252 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11520121 | AATTTTCACCAAGGT[C/G]TTGTGAGACAAGGAA | 10533 |
| rs529183356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512960 | ACTAGATTAGCTAGA[C/T]ACAGAGTGTGGACAC | 10533 |
| rs529191484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399396 | AATAAATTTATAGTT[C/T]AATGTTAAAAAACAA | 10533 |
| rs529193395 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338787 | CTCAGCCAAACTGGG[A/G]CCCAACTAGCTTTCA | 10533 |
| rs529207790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440877 | TTAGTAGAGATGGGG[C/T]TTTGCCATGCTGGTT | 10533 |
| rs529208332 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555513 | CTGCCTGCCTGCTTG[A/G]GGGAGAGGAGTTTCT | 10533 |
| rs529223583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420188 | GTAAGCCACTTATAA[C/T]ACAGATTAACTTCAC | 10533 |
| rs529224143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11484698 | AAAGCTATCCCTCCC[C/T]TGACCCCACGACAGT | 10533 |
| rs529229182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352592 | AGTATAGTTTCTTCA[G/T]TCAACAGATACTTAT | 10533 |
| rs529229347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344625 | CAATCCCAGCAGTTT[A/G]GGAGGCCAAGGTGGG | 10533 |
| rs529232244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11282541 | CACAAACCAATTTGG[C/T]TGACTTGATGATTTG | 10533 |
| rs529236706 | snp | C/T | 1.66092e-05 | 0.00288172 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333047 | GAGAGACGTTGCCCA[C/T]AGCATCATCTTCGAA | 10533 |
| rs529244796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412593 | ACTGTAGCTTTGTAG[C/T]AAGTTTGGAAATCAG | 10533 |
| rs529254372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11318681 | TAGCTTGGCGTTTGA[C/G]GTCTCTTCAGTTCCA | 10533 |
| rs529265263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11381187 | AGCCCATTCTTTCTG[C/T]AGTTTCCTTTAAGAT | 10533 |
| rs529278875 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11421324 | ACGTCTTTAAAAATT[A/G]GAGTTGTCCTCTCAA | 10533 |
| rs529301173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11458896 | TCCTGTCAGATCAGC[A/G]GAGCATTAGATTCTC | 10533 |
| rs529301569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514076 | GACAAGGTCTCAGCC[A/C]CTGTGTTTAGTTTAA | 10533 |
| rs529302108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328319 | TTCCCTAGGCCTCAT[G/T]TAGTAAGAGACTACT | 10533 |
| rs529344020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380660 | GAGTGATTTTTACAT[A/G]CACACTGTATGTGAT | 10533 |
| rs529355487 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426769 | TGCATTTTAAGTCTG[A/C/G]AGACTCCTTTTTAAA | 10533 |
| rs529357381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11419510 | AGTGAGCCAAGATCA[C/T]GTCACTGTACTCCAG | 10533 |
| rs529357850 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542708 | TCCTCCTTTAAGATG[A/T]CAGTCCCCTGGGCAT | 10533 |
| rs529361490 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501184 | ACTTGATCCTGGGAA[G/T]TTGAGGCTGCAGTGA | 10533 |
| rs529376736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338642 | CAACATAGCAAGACC[C/T]TGTCTCAAACAAGAA | 10533 |
| rs529376882 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11465749 | CAACCTGGGCGACAG[A/C]GAGACCCTGCTTCAA | 10533 |
| rs529386864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281848 | AAATCAGGCCTTTGC[C/T]TGGCCCAGTTTTAAA | 10533 |
| rs529391676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544360 | TTAACCCGTGAGGCC[A/C]CCCATCTGCAGAGCC | 10533 |
| rs529397569 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389593 | GTGGGCCTTAAGCTA[C/T]TGCAAGTGTGCCAAA | 10533 |
| rs529425658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485195 | TTTCTCCACATCCTC[A/T]CCAGCACCTGTTGTT | 10533 |
| rs529463271 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468879 | CTGAGTGGACCTAAT[A/G]TATTTTTGTAATGTT | 10533 |
| rs529473547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11441769 | CCTCCCGGGTTCAAG[C/G]AATTCTCCTGCCTCA | 10533 |
| rs529475628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448447 | AGCCCAGATGGCCAG[G/T]CTCAGTGACAGCATC | 10533 |
| rs529487258 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11369821 | CCATGAGTTTTACCC[A/G]CTGGATGAGGCTGTC | 10533 |
| rs529502995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361850 | CTGTATGTAGGTCTG[C/T]TCCTTTATCAGAACA | 10533 |
| rs529508539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485598 | TGCTTTTGGTGTTTT[A/G]GACATGAAGTTCTTG | 10533 |
| rs529509717 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479225 | CAGTGATTCCACAGA[C/G]AAGACTGGCACCTTT | 10533 |
| rs529513060 | in-del | -/TTTA | 0.0417225 | 0.138277 | intron-variant | ATG7 | GRCh38.p7 | 3:11525036 | GCAAATCTCACTTTA[-/TTTA]TTTATTTATTTATTT | 10533 |
| rs529530757 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11540077 | TCTAGGACTAGAATT[G/T]CTGGGTCCTATGGTG | 10533 |
| rs529530942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534400 | ATGCTGTTGGTCTTG[A/G]AACAGAGGCCCTCAG | 10533 |
| rs529535279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400850 | TCACTCAGGGTAATA[A/G]TTTTCTTAGTGAAAC | 10533 |
| rs529547944 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466856 | ATGATGGAGCTGGGC[A/G]TGGTGGCACACACCT | 10533 |
| rs529549279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453401 | AAAGGATATGCTTGC[C/T]AAGAAGATTATTTCC | 10533 |
| rs529559103 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11447803 | AAGGGAAGGGCTGCC[A/T]TGATTGGCCAGCCTG | 10533 |
| rs529574863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368889 | GGTTCTAAAGTACTG[A/G]TAAAAAAAGACCCTG | 10533 |
| rs529579905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453958 | TATGAGAATTATCTA[A/G]GAAAAAGCAGACATC | 10533 |
| rs529581809 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493712 | GTAAATACTTAGATA[C/T]AAAAAACAAAAGTTT | 10533 |
| rs529594526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361149 | CAATGGCTTGACACT[C/G]CCTCCCAGGTAGTTC | 10533 |
| rs529596213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11302276 | TTCTTGCTTTCTAAT[A/G]TTCTTTCCAGTTTTA | 10533 |
| rs529604156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541421 | TGTATTCCTGGTTAT[C/T]CTCATCTCAGTACCA | 10533 |
| rs529604508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496538 | GGACTTTGTGTCCTC[A/G]CTGGACCAGTGCATT | 10533 |
| rs529606780 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11329007 | GCTGAGGCACTAGAA[C/T]TGCTTGAATCCTATG | 10533 |
| rs529620495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547822 | TGTGTCTTTTTCTGG[A/T]GAAATGTCTATCCAA | 10533 |
| rs529632684 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478322 | TAAGACCAAGGTATG[A/G]AAGTATTCATCTGAG | 10533 |
| rs529641313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406602 | TGCTGATAAAGATAT[A/G]CCCAAGACTGGGCAG | 10533 |
| rs529655528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285959 | TCTTTCAGTCTGGGA[C/T]AGCTCCTTGTCTCCC | 10533 |
| rs529658053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491303 | TCACGTAGTTCTCAA[A/G]CCTTGGCTTTCAGCT | 10533 |
| rs529659536 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11335805 | TGGGTTCAAGCGATT[A/C]TCCAGACTCAGCCTC | 10533 |
| rs529665802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415712 | ATAACATGCATAGAG[C/T]TGTCATCTCTTATGA | 10533 |
| rs529666650 | in-del | -/TTTTTG | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11507632 | TAAAGTTATGGGTGT[-/TTTTTG]TTTTTGTTTTTGTTT | 10533 |
| rs529674081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461920 | CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 10533 |
| rs529679481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542026 | AAAAAGGCAAACAAG[A/C]CTGGGGCCCGTGCCC | 10533 |
| rs529685683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455836 | TACTCATCAACCCCA[C/G]AGATGGTTAATTACT | 10533 |
| rs529686562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498585 | CAAACCCCTCCCCAC[G/T]GCTACCAGATTAAAG | 10533 |
| rs529688261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383747 | GCCACCGCATCCAGC[C/T]GTATCCTGGATATAT | 10533 |
| rs529688521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376298 | TAAAAACCACTGAGC[C/T]GTACAGTTTAAAAGA | 10533 |
| rs529689156 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503742 | GCCTGGGCAACAGAC[C/T]GAGACTCTGTCTCAA | 10533 |
| rs529705178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11468840 | ATACCATCTTTGGTC[C/T]AAAATAGATTTGGAA | 10533 |
| rs529710228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553080 | CTGGGCAGGAGGTCC[C/T]GGAGGACACGGCCCA | 10533 |
| rs529718034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292450 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTT | 10533 |
| rs529720975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371048 | GAGATCTGTGCCACA[A/G]GATGGTAGTGAGGCC | 10533 |
| rs529725610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534441 | CACATCTTCTGCTCA[C/T]AGGCAGGTCCTGTGT | 10533 |
| rs529748232 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11554600 | CCCAGCCCTCCCCTG[-/T]TTGGTTCCACCAGGT | 10533 |
| rs529748616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511281 | CCTGTTTTGTCAGGG[C/T]GCTGATTGGTGCGTT | 10533 |
| rs529751627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430039 | TCCTGGAGACAAACA[A/C]TGTTGTTACTTTCCT | 10533 |
| rs529752974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285249 | CAGTGGCACAATCAC[A/G]GCTCACTGCAGACTC | 10533 |
| rs529779042 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11335235 | AGCTCCTGTGTAATG[G/T]TAACTTACATGCTAT | 10533 |
| rs529784833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468359 | TTCCCTGGAAGAACT[A/G]ATGGCTTTTTCCAAG | 10533 |
| rs529789658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11511596 | CCGTACTGTGCGCTC[A/G]CACTCCTCAGCCCTT | 10533 |
| rs529821080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547188 | GGAAGTAGTGAGAGA[A/C]AGTGGAAAAGGCCTC | 10533 |
| rs529826152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315613 | AGCCTTCAAAGGATG[A/T]TTAAGAACATTTCCT | 10533 |
| rs529848259 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315875 | GGACTATAGGTGCCC[A/G]CCACCATGCCTGGCT | 10533 |
| rs529852171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530904 | CGGTGTTGCTTGCCC[C/G]TGGGAGGCAGAGGTT | 10533 |
| rs529855951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409745 | TTTGAGTTATTTTTT[A/G]TGATGGGGTGTAAGG | 10533 |
| rs529858105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488422 | GAACTCCATCCTCCC[A/G]GCGGTCGGGCAGCGG | 10533 |
| rs529871543 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481714 | CTTGGAGCACAGGGC[G/T]TCAGCTCCTATCTTG | 10533 |
| rs529872252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11488622 | AGCCCGCGGGCCTTC[A/G]AGCCTTCTGGGGCCT | 10533 |
| rs529882997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451085 | TTTGACCTTAATGAA[A/G]TGAAAAAGACATTGG | 10533 |
| rs529883164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444367 | TGCCAACAGTTTAGA[A/T]TTTAATTAATACTAA | 10533 |
| rs529901862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523457 | CCACATGTATGACTT[A/G]TTCCCGGACAACCCA | 10533 |
| rs529914530 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11418590 | GGCTTGTCCACACCT[A/G]GCAATTTTTGTCAGC | 10533 |
| rs529924351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482937 | CAGGACTTGAGAAGC[A/C]CCCCCTTGAGCCCCT | 10533 |
| rs529929330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416325 | TTCCCCCAGTGAGCC[C/T]ATCTGGGCCTGGTGC | 10533 |
| rs529935120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11403432 | AATTGTTTCATCTTG[C/T]TTGTGTTCAGAGAAA | 10533 |
| rs529946888 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11365188 | TTGCTAGAAAGGGCT[C/T]AGCAACAGTGTATAT | 10533 |
| rs529952264 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409203 | CTTATAATAGTTTGA[C/G]TTACAATTTTTCAAT | 10533 |
| rs529968970 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11401805 | TAAGTAATGGATGCT[C/T]AGCAAATATTTTTTC | 10533 |
| rs529973154 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279455 | CTTTGGGAGGCCGAG[A/G]CGGGTGGATCACAAG | 10533 |
| rs529979708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322934 | CAGGGCTCTGTCTCT[A/T]CAAAAAATTTAAAAA | 10533 |
| rs529988423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11371440 | GGGCCCTGGGAGGCC[A/G]TTGAACGCTGAGGTG | 10533 |
| rs530000607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499043 | AAACAGTCCATAGCA[G/T]TTCCATTTATTAAGT | 10533 |
| rs530009579 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404624 | GCCATGTTGTATTAG[G/T]CTTTCTCATGCTGCT | 10533 |
| rs530032480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477353 | AATACGTTCAGTAAT[A/G]AATGTAAGTTTCTCC | 10533 |
| rs530033979 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11443249 | CTTCCCCATGAGATC[C/T]ACCTGGCACTCCTAC | 10533 |
| rs530036695 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11391283 | CCTTTTCTTTTCATG[A/T]CAGCTGTAAATCTAG | 10533 |
| rs530042980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469872 | GCATGTACCTGTAAT[C/T]CCAGCTACTTGGAAG | 10533 |
| rs530046574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477808 | ACGCATTCTCTGTCC[A/C]TGTCTCAGCTGAGCT | 10533 |
| rs530057946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384666 | TTTTCTTGTTACTTA[C/T]GAAGCATGAAAGGCT | 10533 |
| rs530064385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11492906 | AACTCCAAGGCCCCA[A/G]AGGGCATGTTACAAT | 10533 |
| rs530065937 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554934 | ACCCCAGGCCTGGTG[A/T]TTCTGGGCCCCTCCT | 10533 |
| rs530070833 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11533163 | AATGCCCGGGGCTTG[G/T]GAGGCCCCTTTGGCT | 10533 |
| rs530073003 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11386202 | GTGAGTCAGTTGAAT[A/G]AGATAAGTTCTGGCT | 10533 |
| rs530083976 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11550275 | ACCTTTGCATTTCCT[-/TTA]TTATGAGTAGGGCTG | 10533 |
| rs530090579 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11390656 | GGTAACTTTTTGACC[-/T]TTGTGGGTGGGTTTG | 10533 |
| rs530092705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444810 | AAATTTTCTCAAACT[A/G]TGCATCTGACAAAGG | 10533 |
| rs530103326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11483588 | GTTATTTTACAGGAG[A/G]TACACAGAAAGCCCC | 10533 |
| rs530117313 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430439 | ACAGAATTCTGCATT[C/T]TACGTAGAAAGGTCT | 10533 |
| rs530122230 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286361 | TTAGTCCTGAAAAAA[C/T]AATAATAGGTTTAGG | 10533 |
| rs530126022 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11391976 | GGGGGGGGTAATTTC[A/C]CTTTAAATTTTTAGC | 10533 |
| rs530134399 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11548837 | ATGCAGCAGGGGATA[A/C]TATCCTTTCGTATAG | 10533 |
| rs530154804 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406560 | CAGTCCTCTTGCCTC[A/G]GCCTCTGTATTAGTC | 10533 |
| rs530156011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11507437 | ACATCAAATAATGAT[A/C]TAGTGTCAATTCTAA | 10533 |
| rs530158011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350532 | GCTAAAGGAGGAACA[A/G]TCATGTGGGTCCTAC | 10533 |
| rs530158230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438617 | TTTAACCTAAATTCT[G/T]TTGTCTCAGAATGGA | 10533 |
| rs530158926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309323 | ATAAAGTCAGGTTCA[A/G]GGAATGTGGTTTCAT | 10533 |
| rs530167573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438063 | GTGATATCCACTTAA[A/G]CATATCTTTTTAATT | 10533 |
| rs530172530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483217 | CAGGTCATGGAGAGG[C/T]AAAGTGATATCCCCA | 10533 |
| rs530196889 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11357752 | ACGGTGGCTCATGCC[G/T]GTAATTCCAGCACTT | 10533 |
| rs530212043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500569 | TCTAGGCCATGTAGA[A/C]AATGATGTGAAAGTT | 10533 |
| rs530214086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464519 | GCAGCCTGGTTCCTA[A/G]GACACCAGCACACTT | 10533 |
| rs530237131 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458333 | CAGCGGCACCATCTC[C/T]GCTCACTGCAAGCTC | 10533 |
| rs530242356 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11318988 | TTGCTTTTCTGCCTG[C/T]CCCATATCCCCAGCC | 10533 |
| rs530256011 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11326514 | TGTGTTAGCCAGGAT[G/T]GTCTTGATCTCCTGA | 10533 |
| rs530275100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457871 | CTTGAAGGGCAAGGA[C/T]TGTGTCTTAGATAAT | 10533 |
| rs530278626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543155 | TTTTCTCCTTTTAAT[C/T]TCCTCATCCCTGGCT | 10533 |
| rs530283171 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448651 | AAGAGAATGATGGAG[G/T]CAAAGCTGGTTGTTG | 10533 |
| rs530302467 | snp | C/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451269 | CAGGCTGGAGTGTAG[C/T]GGCATGATCTTGGCT | 10533 |
| rs530309284 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538652 | GTTCGAGACCACCCT[A/G]GTCAGTGTGATGAAA | 10533 |
| rs530314238 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381755 | TGTGCTATTCCCATA[A/G]CGGTCACTTTTCATG | 10533 |
| rs530317933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343651 | GCTTTATGAATGTGG[A/C]AATTTTTTGGTTACA | 10533 |
| rs530318350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324282 | AAAATTCTGTTTAAC[C/T]GTAGTATAAGCTGGC | 10533 |
| rs530334756 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11536345 | TTGCTATCAATGTGG[A/G]CTCAGGGAATGTGCC | 10533 |
| rs530338614 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11283157 | TTCTTTTGGACTTCT[C/T]GATGACCTGTAGTGG | 10533 |
| rs530364003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465024 | TTATTAAAGATGTAG[A/G]GAGAAGTCATTGGCT | 10533 |
| rs530366510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537942 | TTTCCTTTATACCCA[A/G]TGCCACAGAGCCAAA | 10533 |
| rs530367102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507007 | AAAATCAGGCTGGGC[A/G]CAGTGGCTCATGCCT | 10533 |
| rs530370322 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493414 | TTTGCAAAAGGCAAC[A/G]TTCAATTGGTAAAAA | 10533 |
| rs530390524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463818 | CTTCTCACACCCCAA[A/T]CTCTCATATGTGGGC | 10533 |
| rs530392491 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298488 | ATCACCTAACTGTTT[A/T]CCTCAAAATAATCAA | 10533 |
| rs530415115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423714 | GGTCCTACACTCCCC[C/T]AGCTCTCTAGGACTT | 10533 |
| rs530415502 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ATG7 | GRCh38.p7 | 3:11431389 | CTGCAAGGGCGGGGG[A/G]AAAAAAACAACCACA | 10533 |
| rs530420147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11361241 | ATTTAGTAAGTAAAA[A/G]TATAGGATTCCCAGC | 10533 |
| rs530421322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287449 | TGGGGGCCTGAGAGC[A/G]GCTGCTAAGGAGCAT | 10533 |
| rs530422684 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556794 | GAAAAGTGTTCTCAA[C/T]GATTTTTCCTACAGA | 10533 |
| rs530424538 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506433 | ACATTTCCATCATTG[A/G]TTGGGTGTGGTCATC | 10533 |
| rs530429034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424408 | CACCTGAACCCAGGA[G/T]GTTGAGGCTGCAGTA | 10533 |
| rs530431034 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484284 | CTGTAATCCCAGCTC[C/T]TCAGGAGGCTGAGGC | 10533 |
| rs530435044 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308029 | AGGCTCTGCCCCCAC[A/T]GGAATATCCCACCCC | 10533 |
| rs530439716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480525 | GTGAGCCATGATCAC[A/G]TGACTGCCCTCCAGC | 10533 |
| rs530455349 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11344924 | TCATAAGTCAAATTG[A/G]TTTATAGTCATGTTA | 10533 |
| rs530457220 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447306 | CCATCTCTACTAAAA[A/T]TATAGAAAAAATTAG | 10533 |
| rs530478271 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11346072 | GGCCTTTTTATTTTT[G/T]GGGACAGGTTCTGGC | 10533 |
| rs530487201 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532474 | ATGCCTGTAATCCCA[C/G]TGCTTTGGGAGGCCA | 10533 |
| rs530487203 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11507786 | AGTCCACACTCTAGA[-/G]TGTGGGAAGGAAGAG | 10533 |
| rs530504855 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11306047 | CAGAGAAGAGACCAG[A/T]TTTGTCCACATCTGA | 10533 |
| rs530533496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521614 | CTGGAGCACAGTGGC[A/G]CGATATTGGCTCACT | 10533 |
| rs530535051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11345326 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGTG | 10533 |
| rs530538273 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430181 | TCTTAACTCTGAATA[A/G]GACTGTGTTTTAAGA | 10533 |
| rs530545504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298104 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGT | 10533 |
| rs530564976 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557304 | TTGGCCCCAGCGTAC[A/G]AGGAAGCGTATAAAA | 10533 |
| rs530582041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11283540 | CTCAGCCAATAGGAG[A/G]TGGAGGTGGAATCCA | 10533 |
| rs530582752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11275697 | ACCCTTCTCCAGTGC[A/G]ATTAAGGCCTGATTG | 10533 |
| rs530587625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447744 | TAAGGACTGTGATTG[G/T]CCAGGCCTGGGTCAC | 10533 |
| rs530614370 | snp | C/T | | | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342212 | TAGACTTGGACAAGG[C/T]TGTGTCTGTCAAATG | 10533 |
| rs530616032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527456 | GTCATTCTCTTCTAC[C/T]TGTCCCTGGGTAACT | 10533 |
| rs530652265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375510 | GACAACAACAGGTGT[C/T]GACAAGGACGTGAAG | 10533 |
| rs530653130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11441646 | TCTGTTTCTTCCTTC[C/T]CCTTTCTCCTTTTTT | 10533 |
| rs530669950 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11485100 | TATTTCTAGTTCTAG[A/G]TCCCTGAGGAATCAC | 10533 |
| rs530673620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388575 | CTGGGACTACAGGTG[C/T]CTGCCACCACGCCTG | 10533 |
| rs530701532 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11420881 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGACTAC | 10533 |
| rs530710850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347132 | ACCTCTGGAGAGCTC[A/G]TTCATTCCCACCATT | 10533 |
| rs530721173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420377 | CATTCTGCCCTTGCT[G/T]TTAGTTTTTCCGTGG | 10533 |
| rs530721422 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11367197 | GTTTTGATTAGGGGA[A/C]CATCGTTTCCACGTT | 10533 |
| rs530730150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11327606 | ATCAAGAAGTTTGTA[A/G]CTTGCACATTAGAAT | 10533 |
| rs530733758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11282909 | CTAAGAACATATGCT[C/G]TTTGTCAGCGGGACT | 10533 |
| rs530765378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546344 | GCCCAGCTAAGTTTT[G/T]TATTTTTAGTAGAGA | 10533 |
| rs530770676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407689 | GTGTACTTGCAGGCT[C/G]AAAACCACGTGGAAG | 10533 |
| rs530825804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427311 | TTCTTTAGAAAGAAG[A/G]TATTGGACTCTGGCC | 10533 |
| rs530826052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313965 | TGGTATTTGGTGAAA[C/T]GCTAAGCCAGTAAGG | 10533 |
| rs530828740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306779 | GTGCCTGTTTTTTAG[C/T]TCTTGAGTTATGATA | 10533 |
| rs530837903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427981 | TTAGTTACCTGGATA[A/T]AGAAGCCATGAGGAG | 10533 |
| rs530840122 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456676 | CTTTCTACTCCCCCC[A/G]CTACCGACCACTGTG | 10533 |
| rs530842822 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507782 | TTTTAAGTCCACACT[C/G]TAGATGTGGGAAGGA | 10533 |
| rs530844443 | in-del | -/TTAGTAAAAACATT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11471474 | GCATGTAGTCAGCAC[-/TTAGTAAAAACATT]TAAAAAATTTTTACT | 10533 |
| rs530856878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333223 | TTGTACCTCTTTGCC[A/G]ATGCAGACACCTACT | 10533 |
| rs530857877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484117 | TAAGTCTTCAGGCTG[A/G]GCACAGTGGCTCACA | 10533 |
| rs530859814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362519 | TCACTTAAAGGAACA[A/C]ATGATGCAGTTCCAT | 10533 |
| rs530874512 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461058 | ATGAATCCAATCTAC[A/C/G]ACAATGGGTCAATAT | 10533 |
| rs530874748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11510076 | TTTCTTTATTCTGCC[C/T]GCCCATCTTCTGCCC | 10533 |
| rs530881313 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395403 | AAGCCCAACAAATTT[A/T]TAACAGTACAAATAA | 10533 |
| rs530886575 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406945 | TTCTGGCCCCGTCCC[C/T]CTCAAATTTCGTATC | 10533 |
| rs530897739 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410208 | TGAACAAGAAATATC[A/G]CTTTATTTTTAGATT | 10533 |
| rs530899435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276966 | TCTCCATTCTTGAAT[C/T]TTGCCAATTCCTCTC | 10533 |
| rs530906416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454962 | AGGGTTTTTAAAATA[A/T]TATCAAAACTAGATA | 10533 |
| rs530909987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313252 | TAATAGATGCATTTC[A/G]CCTTAAGTTAATGGT | 10533 |
| rs530931141 | in-del | -/GGAGACACT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11355209 | AGTTCACACGAGCTG[-/GGAGACACT]GGAGTTCTGTATACG | 10533 |
| rs530934685 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384533 | GAGTGATAGGGTAAG[A/G]GTTAGGTAGGAATAA | 10533 |
| rs530956277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486052 | TTCCATATGAACTTT[A/T]AAGTAGTTTTTTCCA | 10533 |
| rs530959753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11497634 | TATCTTAATGCAACT[C/T]GTACAGTGCTTGTCT | 10533 |
| rs530990646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396194 | GCTCATGCCTGTAAT[C/T]CCAGCACTTTTGGAG | 10533 |
| rs530996594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300055 | TTAGCCTCCCAAGTA[A/G]CTGGGACTACAAGCT | 10533 |
| rs530998585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307933 | GTGGCTTGACTGCTC[C/T]TGGGCCTCCTGCTTT | 10533 |
| rs531003634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541025 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 10533 |
| rs531008394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11482025 | TGTAATGAAATGGGG[C/T]TTCAAGGAGCCCTTA | 10533 |
| rs531017127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11414003 | TCTAGGTTATGGTAT[C/T]AGGTTTGTAATTTCA | 10533 |
| rs531028764 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11290747 | TGGAGTGCAATGGTG[C/T]GATCTCAGCTCACTG | 10533 |
| rs531030444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389837 | TGTAATTGACTCTGG[A/T]TTCACTGAAGCATTT | 10533 |
| rs531038549 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11327943 | TGCTGGGGCATGGAC[C/G]ACATTTTGAGGAGTA | 10533 |
| rs531098297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529601 | CGATGTTATCAGCAA[C/T]GTGAAGTTTGTCCCT | 10533 |
| rs531102636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522216 | ACCTCCTTTCAGCTA[A/G]CTGTGCCCTACTTGG | 10533 |
| rs531123211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474881 | TGGGAGTGGGGGGCC[A/G]GAGCCAGTATGGCAG | 10533 |
| rs531136574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475617 | AGTCTGCAGATCAGC[A/G]GGTGATCAGGTAGAC | 10533 |
| rs531159937 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11553401 | TTGAATGGGAGAGTG[A/T]AAGAATGGATGGATT | 10533 |
| rs531164529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410876 | TTATGTACATGAGTG[C/T]ACAACTATTTCTTCA | 10533 |
| rs531164583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11403627 | ATGTTATTGATAATC[A/G]ATTATTAAGTAGGTG | 10533 |
| rs531174754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537903 | ATCCAAAATTGGGAG[C/T]GTCTTGCCCCAAGTC | 10533 |
| rs531176701 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11421316 | ACAGCAGAACGTCTT[A/T]AAAAATTGGAGTTGT | 10533 |
| rs531180402 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11316470 | AATTCTCTCTGTCTT[A/G]TTGAAATTCTATCTC | 10533 |
| rs531194389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443053 | CTGCTTGATTAAAAC[A/G]TCATTTAGAAAAGAC | 10533 |
| rs531214567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11531918 | CAGCTAACATTTATT[A/G]AGTGCTTACTGTGTG | 10533 |
| rs531217634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309493 | AGAAACATGTTTTCT[A/G]TAAGCGAAATCTAAT | 10533 |
| rs531223888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404153 | TTTTTTTTTTTTTGC[A/G]GTAGAGTCTTGCTCT | 10533 |
| rs531232943 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11541048 | GGGACTACAGGTGCC[C/T]ACCACCACACCTGGC | 10533 |
| rs531254680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436216 | ATGATAGCATAATCA[A/G]ATAAGATGCCCAACA | 10533 |
| rs531255780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355875 | AATGAAAACATATAT[A/G]CATGAAAATACTTAT | 10533 |
| rs531265592 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408745 | TAACTATCATGAGAA[A/C]AGCATGGGAAAGACC | 10533 |
| rs531266456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481342 | TATATTTTACGATGA[C/T]AAAAAAATTTAGGGT | 10533 |
| rs531267167 | snp | C/T | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450602 | GGAAGGTTTGGTGTT[C/T]ACCTCATGGAGCTGT | 10533 |
| rs531267601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11506899 | CTCTGCCATTCCCTA[G/T]GTAAGGATTCATAGC | 10533 |
| rs531279983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395806 | TTAGCCGGGCGTGGT[C/G]GTGGGCGCCTGTAGT | 10533 |
| rs531308926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11324165 | CTGATTTGTATTACA[A/G]AAGGAAGTGATTTGC | 10533 |
| rs531310808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457820 | ACTGTGCAGTGGTAG[C/T]GCTTGTGTTGAATAT | 10533 |
| rs531334227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278909 | AAGGCTTCCCTCAGA[A/C]GTGATGATTGAGCTG | 10533 |
| rs531339993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323743 | AACAATTTATATGCT[A/G]TTAGTTGGGCTCTTT | 10533 |
| rs531346913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11317042 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10533 |
| rs531354436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500484 | AAAGACTAAAAACTA[A/G]AAAATAAAACTCCAC | 10533 |
| rs531361257 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ATG7 | GRCh38.p7 | 3:11535465 | TTGTATGGCAATCAC[A/G]GGGGCCAGGCAGGTC | 10533 |
| rs531380181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357942 | TGAGCCCAAGAGGTC[A/G]TGGTTTCCGTGAGCT | 10533 |
| rs531382234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11451793 | ATAGTCTCAAAAAAA[A/C]AAAAAACAAATTAAA | 10533 |
| rs531382552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366197 | GCACTGTGGCCTGGG[C/T]GACAGAGTGAGACTC | 10533 |
| rs531387179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11392038 | CAGGCTGTCTTTGGA[A/G]ATCTTGTCCTTTGAA | 10533 |
| rs531389881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11303792 | AAGAAATTTTCTTTT[C/T]GGCCGGGCGCGGTGG | 10533 |
| rs531411597 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11283966 | AAACTCCCCTGCTCT[-/C]CTAAAGCAAACAGAC | 10533 |
| rs531412875 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11447899 | TGGTCCTCCTCAACA[A/C]ACTGATGCAGATGGA | 10533 |
| rs531412899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543095 | GTCCTCCAACCGACC[C/T]CACGGTGCAGGAGCA | 10533 |
| rs531415430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537385 | TGTCACCTCCACTAG[A/G]CAGGGACCTCCCAGG | 10533 |
| rs531415485 | in-del | -/CG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419510 | AGTGAGCCAAGATCA[-/CG]TCACTGTACTCCAGC | 10533 |
| rs531418272 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337959 | TATCAAAGACACATT[-/A]AAAAAAAAAACTTTT | 10533 |
| rs531429475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11330185 | ATATTTGCCAGGTTT[C/T]TCCACTGTAAAAATA | 10533 |
| rs531435304 | in-del | -/CCAG | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11431204 | GTCAGGAGTTTGAGA[-/CCAG]CCTAGCCAACATGGC | 10533 |
| rs531440144 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555447 | GTGAGCTGCTCAGAC[A/G]TGGCTTTCTGCCTCC | 10533 |
| rs531441533 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11365354 | GGGGTGTCTTTTCAG[A/T]AAAAGAATCCAAAGC | 10533 |
| rs531477175 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357033 | AAAGTTGAAGATAAT[-/A]AAAAAAAATCCACAA | 10533 |
| rs531485912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478001 | GATTCTGATTGCCCC[C/T]ACTTGGCTCATATAC | 10533 |
| rs531492575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352011 | CCCCCCTCCCTCCAC[A/G]CCACGACAGGCACTT | 10533 |
| rs531526842 | snp | A/C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371906 | AAGCTAATTAGACAC[A/C/G]CACAGGTGTGCCTAA | 10533 |
| rs531530763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525702 | TGGAACTACAGGTAC[C/T]CGCCACCACACCTGG | 10533 |
| rs531531833 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528555 | AAATAGTTTGGGCGC[A/G]GTGACTCATTCCTGT | 10533 |
| rs531532453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439568 | GTACAAGCCAGGCTT[G/T]TAGGAGGCAGACGCA | 10533 |
| rs531546101 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292386 | TGCGTCAGCCTCCCA[A/G]ATAGCTGGGATTACA | 10533 |
| rs531548390 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306170 | CCTGGTGGCACGACA[C/G]ATTGACAGGTAGCCC | 10533 |
| rs531549404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478391 | GAGAACCAAACACCC[A/G]TTAATGGTGTGGTCT | 10533 |
| rs531551448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398323 | TTTGCTGGCATAGAC[A/G]GGATAATTAAACAAG | 10533 |
| rs531558373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11385399 | CTTTGCAAATGCACC[A/G]CTTAGAAAGGCAAAT | 10533 |
| rs531564074 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11420265 | CCCTAGAGGATTAAG[-/T]TTTTCCACATATTTT | 10533 |
| rs531567886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11440199 | CTTTCTTACTCTTAA[A/G]CTGGCTTCTAATAAA | 10533 |
| rs531569991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426052 | TTCTAGTTTTGGGCT[A/G]TCATGAATAGCGCTG | 10533 |
| rs531571380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11288811 | AGTTTTATTTTCATT[A/G]AAGTCTGAAATTTGC | 10533 |
| rs531575828 | in-del | -/T | 0.0887219 | 0.191022 | intron-variant | ATG7 | GRCh38.p7 | 3:11441370 | CCTCAACCTCCCGAA[-/T]AGCTGGGATTACAGG | 10533 |
| rs531590435 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500819 | TATTTTTACTAGAGA[C/T]GGGGTTTCACCATGT | 10533 |
| rs531599778 | in-del | -/CCTTGGCCTC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480179 | CTCGAGATCCACCTG[-/CCTTGGCCTC]CCAAAGTGCTGGGAT | 10533 |
| rs531600114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458421 | GGCGCCCACCACCAC[A/G]CCCGGCTAATTTTTT | 10533 |
| rs531602317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465222 | AGCACTTTGGGAGGC[C/T]GAGGCGTGTGGATCC | 10533 |
| rs531628373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532465 | CAGTGCCTCATGCCT[A/G]TAATCCCAGTGCTTT | 10533 |
| rs531635178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544268 | CCTGGGCCTTCACCC[A/G]GCAGCACTTCCCTGT | 10533 |
| rs531644570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373190 | TCCAAAAGGTAGAAA[A/G]TTTACTTTCAGCAAG | 10533 |
| rs531650262 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498264 | GTGCCCCTATTAGAA[C/T]TCCAAAACAGCAATC | 10533 |
| rs531651012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523943 | GTCCCCAGCCCCAGC[A/G]CCCACCCCTTGTCTA | 10533 |
| rs531660006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309128 | AGCCCAGTGTACCAG[C/T]AGAACAGTCTGCTCT | 10533 |
| rs531670228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11489994 | GATGTCTATTAGGTC[C/T]GCTTGGTGCAGAGCT | 10533 |
| rs531677548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483761 | TTATCTGCTTTAATG[A/C]AGTGGGTTTTGTACA | 10533 |
| rs531682873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337243 | GCGGATCATGAGGTC[A/G]GGAGATTGAGACCAT | 10533 |
| rs531703081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11281078 | GACCTGTATGTCCTG[C/T]GTCTATGATTCTTCC | 10533 |
| rs531705764 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278964 | CACTAGATGATGGGT[A/G]TGTGGAGGTGGCCAA | 10533 |
| rs531707575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508432 | GGCCACATGCGTTAG[A/T]CAAGCTTGGTCTAAG | 10533 |
| rs531708894 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539863 | TCCTGCCCTGCACAG[C/T]CGCCTGGAGGTTCAC | 10533 |
| rs531713584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501300 | ATGCTTAGGGAGTTA[C/T]AAGAGGAACAAGAAA | 10533 |
| rs531722847 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455037 | TTCAGCTTTATTTCT[C/T]TCGAGTACAGTTATT | 10533 |
| rs531723269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472131 | ACAGATTTAAGCAAA[C/T]ATGAGAATGTATTTG | 10533 |
| rs531726360 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475842 | TCTTAACTTTGGTTC[A/G]TCTATGTCCATCTCT | 10533 |
| rs531737152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11465697 | TTGAACCCAGGAGGT[C/T]GTGGCTGCAGTGAGC | 10533 |
| rs531754842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539700 | GTCTTAAGCTATATT[C/T]GTTTTCTCTTATGAA | 10533 |
| rs531759656 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298617 | ATTAAACTTTATTAC[A/C]AATGTTCTTTCTCAC | 10533 |
| rs531772548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380546 | CAGAAGCTCTAAAAA[C/T]AGAGCTGGTATGTTA | 10533 |
| rs531775232 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11401163 | TAATCAGAAACTGTG[A/G]GGTTGGGCCCAGCTA | 10533 |
| rs531775396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11533682 | CACATGGAGCTGATT[A/C]TTTAAAGATGTTATT | 10533 |
| rs531791932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296406 | CCACCAAGATACCAA[G/T]TTAGGTCACCTTTTA | 10533 |
| rs531834055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484806 | GTGTTTGGTTTTTTG[G/T]TCTTGCGATAGTTTA | 10533 |
| rs531854989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555929 | TTTCAAATGAGGCTT[C/T]GCTTCTCCCAAAGTA | 10533 |
| rs531857434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447028 | GACACTTGGGTGGCA[C/T]CTTGTCTTTTTCAGA | 10533 |
| rs531860609 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426986 | AAACTATTTGATATT[A/C/T]GCCATATGGAAAAGG | 10533 |
| rs531867006 | in-del | -/AG | 0.0499671 | 0.149956 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557871 | GCACCTGAAATCTAG[-/AG]AGAGAAAGACCTATA | 10533 |
| rs531873605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513301 | TGGAGCAGGGGGCGG[C/T]GCTCGTTGGGGAGGC | 10533 |
| rs531885223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367189 | GCAACCATGTTTTGA[A/T]TAGGGGACCATCGTT | 10533 |
| rs531888946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539078 | AACTTACCACAAAAT[A/G]TTAATGATATCAACT | 10533 |
| rs531893155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411915 | GTTAGGTGAGAGTCC[A/G]ATTTCCTTCTTTTGC | 10533 |
| rs531931878 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481349 | TACGATGATAAAAAA[A/G]TTTAGGGTTCTTACA | 10533 |
| rs531936154 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11384874 | GCTGAGGTGGGAAGA[C/T]CCTTGAGCCCAGAGG | 10533 |
| rs531937838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534262 | ACTGTGCCCTTCTGC[C/T]GCAAGCTGGACTGAG | 10533 |
| rs531939542 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11403707 | TGCTAATGAAAAGGC[A/T]AGGAATATAAAAACC | 10533 |
| rs531940582 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11553363 | GCGTGTGGCACAGAG[C/T]TGGCTACATGAATGT | 10533 |
| rs531951431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317842 | GTGATCCTCCCGCCT[C/T]GCCCTCCCAAAGTGC | 10533 |
| rs531960918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399661 | CTCACTGCAACCTCC[A/G]CTTCCCGGGCTCAGA | 10533 |
| rs531964191 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502262 | AAGTTTTAGGGTACA[C/T]GTGCACATTGTGCAG | 10533 |
| rs531976844 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11377873 | ATTTTGATGTCTCCT[A/G]TTTTGACGTCCTGAA | 10533 |
| rs532000214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475559 | CTGGGAAAAGGGCTG[C/T]GGGGGAGGCTTAGAT | 10533 |
| rs532015948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11419347 | CGCTTGAGGCCAGGA[C/G]TTCTGAGACGAGCCT | 10533 |
| rs532021140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546991 | ACTTGGGAGCCAGGT[C/T]AGGAGCTGGCCTGTC | 10533 |
| rs532036200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511177 | CGTGGAAGGGGACCT[A/G]AGCGGGTTGCCAATG | 10533 |
| rs532060579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11340252 | CTGCAGTTACATTGG[C/T]TTGGCTTGCTTAGAT | 10533 |
| rs532067079 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11436132 | ATAATATAAAGATAC[A/G]GAACTCAATTAAAAA | 10533 |
| rs532072012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11281751 | TGCACTCTAACCTGG[A/G]CAACAAGAGCGAAAC | 10533 |
| rs532076865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412522 | CTATGAATATGTCTT[G/T]TCTTTATGCGGTACT | 10533 |
| rs532083410 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556869 | GGGAGTGAAATGTGT[A/G]CGGGGCAAGGAGAAG | 10533 |
| rs532089938 | snp | A/C | 4.94311e-05 | 0.00497123 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347940 | TACTCCAATCCTGTG[A/C]GGCAGCCTCTCTATG | 10533 |
| rs532104635 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369724 | AAATTATAATGTCAG[C/T]GTTCAGAAGCATCTC | 10533 |
| rs532143305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382851 | TAGTACAAGGAACTC[C/T]GGTATACACTTTACC | 10533 |
| rs532143436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516112 | TCTGTACCAACTGCT[A/G]TGTTAGTTTCTGGGG | 10533 |
| rs532178422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321850 | TTTTTCAGTTTTCAT[C/T]TTCAAAGGAAAATTT | 10533 |
| rs532181924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383238 | CTCTGGCTCCCTTCA[A/G]TCTGGAAAAGTTACT | 10533 |
| rs532193115 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312322 | CAAATACCCACATAT[A/G]TCTGGAATGCTACCA | 10533 |
| rs532212248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536657 | CCGAGAGCGGACCCT[C/G]TTGCCACTGCACCCA | 10533 |
| rs532212711 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11456462 | CGTGTACAAGTTGTT[A/G]TATGAAGTACACGTT | 10533 |
| rs532220763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11363635 | ATCAAGGCATAGTGA[A/G]GATAAGTAAGTGGCC | 10533 |
| rs532230205 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424342 | TAAGAAATATTAAAT[A/C]TTCAATGTTAAATAA | 10533 |
| rs532236399 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11425806 | AATGTCCCTTGTGCC[C/T]CTTACAGTCTCTCTG | 10533 |
| rs532237444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428602 | CTCTTTGAGAGACTT[C/T]AAGGTATTTTTCCCC | 10533 |
| rs532239312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461824 | GAGGTCAGGAGATTG[A/T]GACCATCCTGGCTAA | 10533 |
| rs532270443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510854 | TGGTGCCCCTGGATA[A/G]TTTGCCAGAGTCTGT | 10533 |
| rs532274489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290882 | TGGAGACGGGGTTTC[A/G]CCATGTTGGTCAGGC | 10533 |
| rs532276428 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550454 | TTGCCCAGGCTGGAG[A/G/T]GCAGTGGTGCAGTCA | 10533 |
| rs532284727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422200 | CTTTAAAGCCAGGCA[C/T]TGACTTCTCCTCTGT | 10533 |
| rs532299332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492328 | GCTTCGGCTCGCACA[C/T]GGTGCTCTGCATACA | 10533 |
| rs532299514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536134 | AGGGCTGGTCTGTGA[C/G]GGGGAGGAATTAGAA | 10533 |
| rs532303384 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309824 | TAACATTCTGTCAAA[G/T]GTATGTTTCATAGAT | 10533 |
| rs532312696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370995 | TGGACCCTTGGGCAA[C/G]CCATGTCACTTTCCT | 10533 |
| rs532323737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482809 | TTTTTTTTTTTGAGG[C/T]TTATATCATTTGTAT | 10533 |
| rs532338141 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11341652 | AGGGTTTTACCATGT[G/T]GGCTAGGCTGGTCTC | 10533 |
| rs532338602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328915 | AACATGGCGTAACCC[C/T]GTCTCTACTGAAAAA | 10533 |
| rs532351084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11529747 | TGGCAGGGGACACCC[C/T]ACACGTCATCGTGGT | 10533 |
| rs532359044 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11314928 | ACCCTGTCTCAAAAA[G/T]TAGTAAATGGGTGAG | 10533 |
| rs532363793 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11408858 | GGGGACACAGCAAAT[C/T]CATATTAGTCTCCCA | 10533 |
| rs532367094 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11301940 | TTTGAACTTACTACA[A/G]AATGTGAGCATCTTA | 10533 |
| rs532377282 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11329345 | GTTTAGGGTGATTCC[A/T]TCCTTACAGAACTAA | 10533 |
| rs532384585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11483187 | AGCATTCTCCCCGTC[C/T]CCCTGCCCCTAACCC | 10533 |
| rs532385666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11450055 | GGTCTGTTTCTTCTT[A/T]GGATAATAATGATGT | 10533 |
| rs532388856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476496 | CCATTTCAATTAGAA[C/T]CTTGTATCAGAATAT | 10533 |
| rs532403358 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11399708 | GCCTCCCGAGTAGCC[A/G]GGATTATAGGCATAA | 10533 |
| rs532407584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438125 | GGGAGACACAATTAC[C/T]CTATTAGGCAACATG | 10533 |
| rs532409795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504541 | GCAGCTGGGCCTGAA[A/G]CACTGAGGATGACTA | 10533 |
| rs532412017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528774 | GAGGTTGCAGTGAGC[C/T]GAGATGGTGCCATTG | 10533 |
| rs532424568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302067 | TATTTTTTCTTTAAC[C/T]GTTGAATACCCTCAG | 10533 |
| rs532425389 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279219 | GACATTGACCAGAGG[C/G]CATTACTGCATTTAT | 10533 |
| rs532426323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415116 | TACAGTATGTAACTG[C/T]AATGAACACTGTAGA | 10533 |
| rs532433821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11328465 | TTTGTATTAAATTAA[A/G]TACGAATCTGTCTAT | 10533 |
| rs532448890 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11498471 | TCACTTGCTATATGG[C/G]CCACCTGCCTCTACC | 10533 |
| rs532450616 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531419 | CCTGGCAAGGCAAAG[A/C]ACCTTCCTGAGGTCC | 10533 |
| rs532450719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500700 | TTACCCAGGCCGGAC[A/G]TCTCACTGCAACCTC | 10533 |
| rs532452355 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11420441 | AACATACAATCTGAA[C/T]GTTTAACTGGAGTCT | 10533 |
| rs532466988 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341635 | GTAATTTTAGTAGAG[A/G]GAGGGTTTTACCATG | 10533 |
| rs532478182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11284996 | GGACTATAGGCGCCC[A/G]CCACCATGCCCAGCT | 10533 |
| rs532480101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11277185 | TTTTGCCTGTCTTTC[C/T]GCACAGCCTCCCAGC | 10533 |
| rs532484295 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11507214 | TTGAACCCAGGAGGC[-/G]GAAGTTTCAGTGAGC | 10533 |
| rs532487816 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392069 | AAGGGAATGCTGATA[A/C]CCAGAGGAATGTATT | 10533 |
| rs532489863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356933 | TCCTTTCTGCCTCAG[G/T]TCCTTTCCTGCTTTG | 10533 |
| rs532493658 | in-del | -/AA | 0.00438332 | 0.0466095 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557940 | TACATTAAAAAAAAC[-/AA]AAACAGTAACAACAA | 10533 |
| rs532498030 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456066 | CAGAGTTGTGTAACC[A/G]TCATTGTCTGTTTAG | 10533 |
| rs532518588 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11456516 | GGAGTGGAATTGCTG[-/T]TATTGTGTCGTAACT | 10533 |
| rs532536460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488364 | CTCCCGGGCGGCACT[C/T]GCCGGCGCGGCGGCA | 10533 |
| rs532537639 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11308719 | AGGCATGAAAATGGC[C/T]TGGTTGCCCCCTCGG | 10533 |
| rs532551248 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325835 | TGTCTCTGTAGGAAC[A/G/T]GCATTTTCTAGATTG | 10533 |
| rs532553354 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11517048 | AGATCGCACCACCAC[A/T]CTCTAGCCTGGGCGA | 10533 |
| rs532562842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423557 | ACATTTTTTCCTGAC[A/G]TAACATTCTGGTTTA | 10533 |
| rs532574025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554053 | GGCTCTCTCCCTGGG[A/G]GCTGACACCAAGGAC | 10533 |
| rs532586528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437907 | AGAATAATTCCATAA[C/T]ACCACCTAAAATCCA | 10533 |
| rs532590986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469803 | AACAGCCTGAACAAC[A/G]TGGTGAAATCCCATC | 10533 |
| rs532599268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463713 | CTCCCTGCAGACTGG[C/T]GTCTTCTGCTAGACA | 10533 |
| rs532612528 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367110 | AAATTAATCAGGGTT[G/T]TGTGGTCCCCATGTA | 10533 |
| rs532642820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11530353 | CCGTACTCCGAGAAG[C/T]ACTCTGCATCGCCAC | 10533 |
| rs532652183 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285781 | ACTATTTTATTTTGG[A/T]ACAGTTTCAAACTTA | 10533 |
| rs532658655 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558013 | GTTTTTCAGCAGTTT[A/G]CCCTCAGAGTTCTGG | 10533 |
| rs532673685 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313988 | CAGTAAGGGGGAATT[A/C]TAGGAATATTTTGAA | 10533 |
| rs532682753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402838 | ACACCCAGTTTATTT[A/G]ACAATCGACGTCAAC | 10533 |
| rs532686570 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404678 | GTAATTTATAAGGGA[A/G]AGAGGTTTAATGGAC | 10533 |
| rs532717203 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11550222 | TGAAATGCAAACCCA[-/T]TTTTTTTTTCTGGTT | 10533 |
| rs532717776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554604 | AGCCCTCCCCTGTTG[A/G]TTCCACCAGGTGGTT | 10533 |
| rs532719223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329678 | GATAATTTTAGATTT[A/C]CAGAAGATAGTGGCA | 10533 |
| rs532720860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336349 | ATGCTGACATTTAAA[C/T]TCAGGAACCACACCG | 10533 |
| rs532728548 | in-del | -/AG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440013 | CATAAGGCTGGAATC[-/AG]AGAGGAAGAAGTGCA | 10533 |
| rs532743837 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466699 | GTTGTATGAAGGATT[A/T]TAGCACCTTTATGTT | 10533 |
| rs532749146 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381414 | TATGGCTTTATGTTG[G/T]TCTGGCTAGTCAATG | 10533 |
| rs532775565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304599 | TATTCCGTTCTGACC[A/G]CCTGCCTGCCTGTTG | 10533 |
| rs532788310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393601 | CTTTGGCCTGCCATG[G/T]TGTTTTAGTCAGAGC | 10533 |
| rs532796460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542656 | CCTCTTTCCCAGCCT[A/G]GTAGCTGCTCTCAAC | 10533 |
| rs532797484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11344688 | CCTGCACAACGTGGC[A/G]AAACTCCATCTCTAC | 10533 |
| rs532800799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549239 | GATGTCTTCTGTGTT[A/G]GGGTTGTTTTCTTAA | 10533 |
| rs532804213 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413863 | CAGGTGCAGGGCTTT[C/T]GTTTGCCAGGAGATT | 10533 |
| rs532807747 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11479491 | TTCCAAAGCCCAGAT[A/T]TTGACCGATCCCCTC | 10533 |
| rs532819801 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368752 | CAAAAAAAAAAAAAA[A/G]GGAATCAAGGTGACG | 10533 |
| rs532838204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446382 | TATGCCAGAGACTCT[G/T]TATTTGTAAGACTAT | 10533 |
| rs532851984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430297 | AAATGTGTGTATGCG[C/T]ATATAAGCAAAATAT | 10533 |
| rs532866525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430939 | GTAGAGAAGGGAAGG[C/G]CAAGAAGCCTAGGGC | 10533 |
| rs532869287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11360034 | AGAAATGTTTGTTAT[A/G]AGTTTTTTTGTTTGC | 10533 |
| rs532870330 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469215 | AGCACTTTGGGAGGC[A/C/T]GAGGCAGGTGGATCA | 10533 |
| rs532872095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342752 | TTATTTAATCAATTT[C/T]AGATTACTTTCTATT | 10533 |
| rs532890355 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11352247 | TTCTTAATCCAGTCT[A/G]TCATTGATGGACATT | 10533 |
| rs532902237 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465838 | ATAAAAATTAAAAAC[C/G]CAGGGATAAGAAGAA | 10533 |
| rs532904027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11490551 | CTCGTTAGTTGATGC[A/G]GTTTCTTCCTAGCCT | 10533 |
| rs532927836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399485 | TAGAGAAATTATTAT[A/G]TAAGTCGCTGGTTTT | 10533 |
| rs532932454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399073 | CAGATGCAGGCTGGG[C/T]GCAGTGGCTCACGCC | 10533 |
| rs532937315 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542903 | TGTTCCTTCAGACTC[C/T]TAGCTCCTTGTCAGT | 10533 |
| rs532976682 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11272754 | AACACGGGAGATGGG[-/A]ACATTTGGATTCCCA | 10533 |
| rs532982607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441100 | CAAATATGTAAACTG[A/C]TGTGGGATATTTTTG | 10533 |
| rs532986380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11352633 | CCTTCTACCAGGCCA[C/T]GGAGAAAAGGCTTGA | 10533 |
| rs533005863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452797 | GATAGGAGATAATTA[C/T]TGCAGATATTAGTGT | 10533 |
| rs533019092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394261 | GTAAGACCATGTACT[A/G]AGGATATATTATATA | 10533 |
| rs533021999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545089 | GAAGCCTGTGAAAAG[G/T]CTGAGCAAGGGGAGA | 10533 |
| rs533034757 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11416489 | TTATCAAATTTCTAG[A/G]TACGGAGTTGTTGAT | 10533 |
| rs533065744 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11361986 | TGACTGGCTTTTATG[C/T]CCTCCCAATATAAAG | 10533 |
| rs533072102 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464522 | GCCTGGTTCCTAGGA[C/T]ACCAGCACACTTCTG | 10533 |
| rs533076630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513475 | CGCACCCTCTGCAGC[C/T]GCTGGCCTGGGTGCT | 10533 |
| rs533103295 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303273 | AGAAGACTGGGAAGC[G/T]TGGAACCCAGCTAAA | 10533 |
| rs533104527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11310878 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 10533 |
| rs533106105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318425 | ACGGGTGATACTTTG[A/G]TTGGTCTTCTATGCC | 10533 |
| rs533111402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406664 | AGTTCCACATGGCTG[A/G]GGAGGCCTCACAATC | 10533 |
| rs533111552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413930 | TCTATTCAGATTTTC[A/C]ATTTCCTTGTGATTT | 10533 |
| rs533116629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332391 | TTAATGACTGAGAGA[A/T]GGCATAAGACAGCCT | 10533 |
| rs533118446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551540 | GGATTCTGTACATCC[A/G]ATGTTAGGTTTATTC | 10533 |
| rs533129420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276257 | TCTTTAGCTGACCCT[A/G]TCCTTTTGCCTTTTA | 10533 |
| rs533143343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11327473 | CTAGAGAGGTCTGGG[A/G]TCAGATTGAGTGTAT | 10533 |
| rs533171752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407161 | TACAGCCATTCCAAA[C/T]TGGAGAAATTGACCA | 10533 |
| rs533184555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319811 | TGAATGTCTCTCAGC[C/T]TACCACCTTGCGTTT | 10533 |
| rs533237854 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11345266 | AAAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 10533 |
| rs533255853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521101 | TAAAAATGCCTGTCT[C/T]GCAGCAATGCTGAGA | 10533 |
| rs533260463 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11362340 | TGAGAGGCACATAGG[A/T]ACTGAGGGCCGCAGG | 10533 |
| rs533269748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496057 | GATGAGGAGGCTAAA[A/G]CAGGAGAGTTTAAGT | 10533 |
| rs533275707 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556596 | TACAGACAAATCTAC[A/G]ACAAAAAAAAAGATC | 10533 |
| rs533285113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11338712 | AAATACCACATCAGA[A/G]TGCCCGATTTAAAAG | 10533 |
| rs533285874 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11480045 | ACATTCTCCTGCCTC[A/C]GCCTCCCAAGTAGCT | 10533 |
| rs533293059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413261 | ATCTTAGAGAGAAAG[C/T]GTTCCTTCTTTCATC | 10533 |
| rs533298771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503397 | AGAACATATAATATG[C/T]ACATATATCTTATCC | 10533 |
| rs533308113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420819 | GGAGTGCAATGGCGC[A/G]ATCTCGGCTCACTGC | 10533 |
| rs533321163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11529062 | TGGAAGGCACTGTGG[A/G]AAAAAGGGGGCGGTA | 10533 |
| rs533323728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11496756 | TGGGATGTATTATCA[C/T]ACTTTCTGAAGCTGG | 10533 |
| rs533336690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521709 | AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 10533 |
| rs533352701 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11401392 | GGCTTATGTCAGTCA[A/T]GTATGTGTTGGTTTA | 10533 |
| rs533375677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11435130 | AAGTGTTTAAAAATA[C/T]ATCAAAGTACTTACT | 10533 |
| rs533384148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395747 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 10533 |
| rs533399817 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468982 | GGTGCACAGCTGCCC[A/G]ATCTTGTTGGGTTGT | 10533 |
| rs533402339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354756 | AATGAGTAGTGGATA[C/T]TGGACTAGCTCTGCC | 10533 |
| rs533411525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369595 | TAGTAGAGTCTGGTT[C/T]CAGTGGGGAGGCCTC | 10533 |
| rs533427833 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11459518 | TTTTTTTTTAAGTGA[C/T]TATGTTAGGAAACTT | 10533 |
| rs533436716 | in-del | -/TTTA/TTTATTTA | 0.225557 | 0.255377 | intron-variant | ATG7 | GRCh38.p7 | 3:11525039 | ATCTCACTTTATTTA[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 10533 |
| rs533456388 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11328598 | TCTTTGAAATAATAC[A/G]GTAAATATCTGATAA | 10533 |
| rs533457802 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11275594 | CCATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 10533 |
| rs533469280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449135 | CATCCTGTGAAGGAA[C/T]GCAGCGTGAGCTTGT | 10533 |
| rs533474752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11368969 | TTCTCAGCTTCATGA[A/G]TTCTTTTAGCTTCAG | 10533 |
| rs533481228 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471421 | AAAAATATATGACTT[A/G]GTCATCTTTATACCC | 10533 |
| rs533494245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313127 | CTATTTTGGGAATAC[A/G]AAAGTCCTTTATTTG | 10533 |
| rs533497166 | snp | C/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272241 | GGGCGTCACCGCCCC[C/T]TGATGCCCCGCCCTC | 10533 |
| rs533500651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326805 | TTAATTCGGTGGAAG[A/C]CCTGGACTGGAAATC | 10533 |
| rs533502601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529945 | CACCATCCTCTTGCC[C/T]AGGAGACAGGAGGGG | 10533 |
| rs533504159 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11387670 | CAGTCACCACTGTTC[A/C]CCTTAAAAATGCAAA | 10533 |
| rs533507429 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11402560 | ATTTGACCTAGGTTT[C/T]ACCTAGAACCTCCTT | 10533 |
| rs533520471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480612 | CTGTGCTCACTGGTT[C/T]CCTCGACTTCACCTA | 10533 |
| rs533523661 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448660 | ATGGAGGCAAAGCTG[G/T]TTGTTGTTGAACAAA | 10533 |
| rs533531270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450248 | CAAGTCGTTTGGCTC[C/T]AGAGCCTGTGTTCTT | 10533 |
| rs533578605 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355334 | TGGTCTTGTGATAAA[C/G/T]ATTTCTTAGGACCTA | 10533 |
| rs533585535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11481279 | GAATGCACTTAACGC[C/T]ACTGAACTGTGCAGT | 10533 |
| rs533649162 | in-del | -/CT | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11275336 | TTCGCTAATGTCTTC[-/CT]CTCCTCTTTTTTTTT | 10533 |
| rs533672528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314400 | AGGGAGCAGCCATTA[C/T]TGATTAAATTTTTTT | 10533 |
| rs533683894 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270664 | CAATGTTTTGGGGGT[A/G]GGGGGTGGATCTCAC | 10533 |
| rs533690088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11408536 | ATGCTGTTGATAAAG[A/G]CATACCCGAGACTGG | 10533 |
| rs533701067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476808 | TTCTGAAAGAACATT[A/T]ATGTTAACTTTCTTT | 10533 |
| rs533708344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400898 | GGAATGAATTTTTTT[A/G]CCGTAAGTAATTTAT | 10533 |
| rs533722442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517218 | TGGTAGCGCATGCCT[A/G]TAATCCCAGCTACTG | 10533 |
| rs533722503 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11329392 | CAAAAATTTATCAGC[C/T]GTGTTTTCATTTAAC | 10533 |
| rs533733081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554195 | TGCGAGGCTCAGACT[C/T]GGAGGACACGCATTG | 10533 |
| rs533733182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11492836 | GGCCACTTTGGTGCT[A/G]GAAGGAACAAACTTT | 10533 |
| rs533734141 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11518998 | AAAAAAAAAATCTTA[C/T]ATAAGTAAATATAGA | 10533 |
| rs533748180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492934 | AATGCTCTCTTAGCT[C/T]CGCCGTCCATGGACA | 10533 |
| rs533753230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469374 | TAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 10533 |
| rs533771401 | snp | A/C | 1.65723e-05 | 0.00287852 | intron-variant | ATG7 | GRCh38.p7 | 3:11554793 | ATCTCGGCTGAGCCT[A/C]TCCCCTTCTCCATGC | 10533 |
| rs533777831 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11364420 | TGGATCTGAAGCACA[G/T]AAAAGTTAAGCAACT | 10533 |
| rs533780500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396545 | GAAATTTAAGGCCGA[A/G]GTGGGCGGATCACTC | 10533 |
| rs533787076 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11275765 | TGTTAATTGGTAGTC[A/C]GTAGGTATTACCATG | 10533 |
| rs533789597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444406 | GTTTGTCAGATAGGG[C/G]TGAGCTTTGGAGAGC | 10533 |
| rs533822373 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11388528 | CCGCCTCCCAGGTTC[A/T]TGCCATTCTCCTGCC | 10533 |
| rs533823656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450690 | GAGAGTTGCAGGGAT[A/G]TTAAATTTTTGCACA | 10533 |
| rs533828310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523473 | TTCCCGGACAACCCA[C/T]TCTTCCTTTAGGCAG | 10533 |
| rs533831966 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356811 | ACTTAATGGATTAAT[C/T]AATGAGATCCTGATA | 10533 |
| rs533832222 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359571 | TGTGGTGATGCACAC[C/T]CGTGCTCCCAGCTAC | 10533 |
| rs533842736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341694 | CTCAGGTGATCCGCC[C/T]GCTTTGGCCTCCCAA | 10533 |
| rs533842843 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11491530 | GGAGCTGCGTTCCTT[G/T]GGAGGAGGAGAGGCG | 10533 |
| rs533850571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519646 | CTCACTGCAAGCTCC[C/G]CCTCCCAGATTCACG | 10533 |
| rs533861645 | in-del | -/CATCTCTCTGCCTGCAGA | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11318789 | TGCCGCAGCTTCCCC[-/CATCTCTCTGCCTGCAGA]CATCTCTCTGTCTCC | 10533 |
| rs533883497 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271423 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 10533 |
| rs533906773 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272118 | GGTGATCATTCCTGT[C/T]ATCCTCTGAAATCAA | 10533 |
| rs533919479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277743 | ACAGAAAACAGGGTT[C/T]GAGAGCAGAGAACTG | 10533 |
| rs533921683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463879 | AGTCAAGTTAGACTA[G/T]AGAGGCAGAGTCTGT | 10533 |
| rs533940303 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11289374 | GTTACATAGACGTGT[A/G]TGTTCCTAAGTGATA | 10533 |
| rs533941270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457544 | TACCCAGGAGTTCAA[C/T]AAACACTAAATGTGT | 10533 |
| rs533943139 | in-del | -/TCCC | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11368287 | AGAAACACTGCTTTT[-/TCCC]TCCCGGCTGGTGGCT | 10533 |
| rs533947299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278571 | GCACCTGTGAGGTGC[A/G]AAGACTGGTGTTAGA | 10533 |
| rs533958402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293198 | CTAGAAGTACAGTCC[G/T]GAGATTCATTGGCAT | 10533 |
| rs533962353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390872 | CTGGCAGGACATTTT[G/T]ATATGACTAGTGCAG | 10533 |
| rs533962555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500173 | CGCGCAACATAAAGA[A/G]CAATATGAACACAGT | 10533 |
| rs533976642 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372418 | TCGTACTTTTCTGCA[C/G]TGTTTTGAAAAATTA | 10533 |
| rs533980130 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420209 | TTAACTTCACAGCAC[A/G]TAAAAAGAATACTGG | 10533 |
| rs533986882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11511674 | GGGGAGGCTCCGGCC[A/G]CACAGGAGCCCATGG | 10533 |
| rs533997209 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11293757 | TTGGGAGTCTGAGGC[A/G]GGAGAATCACGTGAA | 10533 |
| rs534011931 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11470916 | CTTTGAGGTGCAGAT[A/G]GTCCCCTTCTCCAGA | 10533 |
| rs534013735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336063 | TTTTTTTTTTTTGAG[A/G]CAGTCTCGCTCTGTT | 10533 |
| rs534026860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11423295 | GCCCCAAAACAATTA[C/T]AATAGTAACATCAAA | 10533 |
| rs534033380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11395186 | TAGTGAAATGGAAAA[C/T]AGGTTAGAAGAAACT | 10533 |
| rs534052707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11463240 | TCCCTAACTACTACT[A/G]ACTTCAGCTTGCAGC | 10533 |
| rs534054066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329812 | AATTCTTACATTACT[A/G]TTAACTCAGCTCTAG | 10533 |
| rs534057120 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537791 | TGATAACCTCTGTAT[G/T]GTTGGTGGTAAAATG | 10533 |
| rs534059145 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11488444 | GGGCAGCGGCGGCTG[C/T]GGTCGGTCGCGGCAG | 10533 |
| rs534065147 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516031 | GCTCACATTCCTTTT[A/T]AAAAAAAAAAAAAAA | 10533 |
| rs534097812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349712 | GTTTACAGTGGCTCA[A/G]ATCTAATGTGTTATT | 10533 |
| rs534104694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11398032 | GTGGTTGAAGTGAGT[C/T]GAGATCACACCACTG | 10533 |
| rs534113653 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551176 | CGTGTCCTGCGGGCC[A/G]TCTGAGTGTTCCGTG | 10533 |
| rs534113898 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11323338 | AACTCCAGCACAACA[C/T]TGCTTATCATAAATG | 10533 |
| rs534118880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366411 | GCATTTTTTTTTGAC[A/G]TGCATGTGTTAATCT | 10533 |
| rs534128534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11390280 | ACAGATTTTTTAAAA[A/G]GTGAGTGCAAAATGA | 10533 |
| rs534131389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397044 | AACAAGTACAAGATA[C/T]AAAGCACAAGAAGTC | 10533 |
| rs534143688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308884 | GTGCTGGGCCTGTAG[A/G]AAAGAAGAGCCTGGT | 10533 |
| rs534147640 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379479 | CTGTTCCAAATCAAG[C/T]AAATAACTGGATATA | 10533 |
| rs534150358 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11417327 | CTTGCCGTACTGTTA[G/T]TTTTTACCTCATGTA | 10533 |
| rs534160041 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11315214 | TTCACTTGCTGTAAT[-/A]AGAGTAAGAGGAGTG | 10533 |
| rs534164680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279265 | GATGCTCAACATTCT[G/T]CAGTGTGCAGGGATA | 10533 |
| rs534190606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286894 | GCAGGTGTGAGCCAC[C/T]GCACCCAACCTTTTT | 10533 |
| rs534196115 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11378673 | CTGGGCGACAGAGTG[A/G]GACTCCATCTCCAAA | 10533 |
| rs534196704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457901 | TATACCCTCAGGACC[A/G]GACCTAGTGCATTGC | 10533 |
| rs534230089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543270 | GTTCCTGGAACCCCG[A/G]AGCAGTGGGTGTCAT | 10533 |
| rs534231679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358200 | TGTCTCTGTTTGCTG[C/G]CCTGCCCTGCCTCAG | 10533 |
| rs534275174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11330737 | AAAGAGCTGTGAAAG[C/T]AGCAAGGACAGGCCA | 10533 |
| rs534285787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505788 | GAAAGTATCAGTAGG[C/T]TCCGTGGCTTAAGTG | 10533 |
| rs534287390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431039 | TGTACTTGGAGCCAC[A/C]GTTACCTGAAGTCAA | 10533 |
| rs534287625 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11511823 | CTCAGTACACCCTCC[A/G]CAGCCACTGGCCCAG | 10533 |
| rs534293818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416712 | GTGTCATTGATTTCT[C/T]CTCTAGTTTTTATTC | 10533 |
| rs534300906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381494 | CTTGTTCTATTTCTA[A/G]TTAAATTAGCCTTTC | 10533 |
| rs534306141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423862 | TTATTCTGCCAGTCC[C/T]TTGGCTTAGATGGGT | 10533 |
| rs534318541 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11443070 | CATTTAGAAAAGACA[C/T]TCTTCCCTGTTTTGA | 10533 |
| rs534324267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11506408 | TACTGTATTGGACAG[C/T]ACAGATAAAACATTT | 10533 |
| rs534327761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469921 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 10533 |
| rs534330738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11374772 | AGCCAGGCGTGGTGG[C/T]GGGTGCCTGTAGTCC | 10533 |
| rs534355686 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11404402 | TGGCCTCCCAAAGTG[C/G]TGGGATACGGGCATG | 10533 |
| rs534364529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309640 | AGGGAAAAGGTAAGG[A/G]TCGATTATAGAGATA | 10533 |
| rs534383588 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556871 | GAGTGAAATGTGTGC[A/G]GGGCAAGGAGAAGGG | 10533 |
| rs534390851 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479591 | TCAAGTTGGAAGCCC[A/C]AAGTAAGGCATGTTT | 10533 |
| rs534397808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338927 | TTTTTTTAAATGTCA[A/G]CAGCTGAAAAGTTTC | 10533 |
| rs534413653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398478 | CTTATAAAACTCATT[A/G]ATTAAGGATGACATA | 10533 |
| rs534424234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11427362 | GCCTGGCTTTTTCAC[A/G]ATTTGATCAGTCTTC | 10533 |
| rs534441680 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11370489 | GCATCCAAGATCGAT[C/G]TGGAGTTTGGAGTTA | 10533 |
| rs534447010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466071 | GCTCCGTTTTAGAAC[C/T]TAAAGTCTGCGGCTT | 10533 |
| rs534447191 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11473373 | TTCCTGCAAATCATC[C/G]CATTTATTTTTCATA | 10533 |
| rs534452944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11502317 | CCATGCTGGTGTGCT[A/G]CACCCACTAACTCGT | 10533 |
| rs534456069 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412842 | TTTATTTATGATGGG[A/G]TGTATTTCCATTTAT | 10533 |
| rs534457100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11388123 | GATATGAGAGTTGCA[A/G]CCAGTCCCACCATGG | 10533 |
| rs534469499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407320 | CATGATTGGTTCCCA[C/T]GGTCTTGGGCAGCTC | 10533 |
| rs534473374 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395075 | GGAAACTCTAAAATA[C/T]GGCTTTCCAGATTTA | 10533 |
| rs534478223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491855 | CTCAGAGGAGTACCC[A/G]GCCGTGTGAGGTATC | 10533 |
| rs534479536 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant, missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11379984 | TAGATCCGGGGATTT[C/T]TTTCACGGTTTGATA | 10533 |
| rs534501256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323817 | TTTGAAGTGCATTAG[A/G]TATTTCAGTTTTTTC | 10533 |
| rs534503955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454433 | TGGAATTTGACGGCA[C/T]GAGTCTGGGCTGGGG | 10533 |
| rs534531365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401087 | CCGAGCACCAGCAGC[A/G]TCAGTGCCATTTGGG | 10533 |
| rs534538108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272500 | GAGGCCTGGAGTCAA[A/G]GGGCGAGCTCGCCAG | 10533 |
| rs534560325 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369200 | TTATCTCAGTGTGCT[A/C/T]CTAGGGACATGGACA | 10533 |
| rs534560901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11326391 | GCAACCTCCACCTCC[C/T]GGGTTCACACCATTC | 10533 |
| rs534582610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11275317 | TCTACCCATGGAAAT[A/G]ACGTTCGCTAATGTC | 10533 |
| rs534586200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460556 | GCTGCATGGCTTCTG[A/G]GGTTATTTTCCCTCA | 10533 |
| rs534597044 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422316 | AATTTTCTGAGCTAG[A/C]TCTCATAATAACATG | 10533 |
| rs534609343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11491472 | CTTCTTCTCTCAACT[C/T]GTCAAAGTCATTCTC | 10533 |
| rs534611500 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11327045 | TCCTGCTCTAGCTGC[C/T]TCCCAGGATCCCTGC | 10533 |
| rs534617992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496931 | GTGGTGTGATCTCGG[A/C]TCACTGCAACCTCTG | 10533 |
| rs534637947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11539802 | AAACGTACTCGCTTG[C/T]GGAACCAGCACAGTT | 10533 |
| rs534645474 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11431325 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGCTG | 10533 |
| rs534647687 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11317878 | TTACAGGCGTGAGCC[A/C]CTGTGCCCGGCCACA | 10533 |
| rs534654580 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11460298 | GTCCTCTTGTCCTTC[A/G]GTATCTTATCTACCT | 10533 |
| rs534662161 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508503 | TCTGTGGCCCAGGCT[A/G]GAATGCAGTGGCCTG | 10533 |
| rs534664009 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11306689 | AATAGGAAATGAACT[-/TC]TCTTTGGGGGACAGT | 10533 |
| rs534672077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11515334 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCTAGG | 10533 |
| rs534679546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291090 | CTCTGGCACTGGTAA[A/G]ATTCCATCTTGATGT | 10533 |
| rs534685624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388861 | GAAACAAGGGAGCCA[A/T]CAGCTGGAACTGGGA | 10533 |
| rs534704542 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11281019 | CTGTATCTTCACCTT[A/G]TCTACCGGGATTTCT | 10533 |
| rs534708946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419919 | GAGTCATTATTACTT[C/G]TCTATTTTGCAAACT | 10533 |
| rs534715940 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322529 | ACAAACTTTTTGTAT[A/G]TTTCCTTTTAATCCT | 10533 |
| rs534720642 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11551770 | TTTTTTTTTCTCGAG[G/T]CAGGGTCTCACCCTG | 10533 |
| rs534730469 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11475044 | ACTTTTTTTTTTTTT[A/T]AAATCCTGGCCACTG | 10533 |
| rs534736075 | in-del | -/T | 0.376195 | 0.215812 | intron-variant | ATG7 | GRCh38.p7 | 3:11299928 | AGAGAAGAGACACAC[-/T]TTTTTTTTTTTTTTG | 10533 |
| rs534738194 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459915 | ATATTAAAAATCCTT[A/G/T]CAAGAGCCCTGTGTG | 10533 |
| rs534739420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11412294 | AGTAGGCCTGAAGGT[C/T]CTTTCCTGAGGGAAG | 10533 |
| rs534739709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332736 | GATTGTAGAAAGAAA[C/T]CACCTAGAAAGAAAT | 10533 |
| rs534740760 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11282820 | TTGTCTATAAAATGT[G/T]CATTGGCTCCATATG | 10533 |
| rs534780038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320067 | GCCTGGCCCCTGTGG[G/T]CATCCAGCCCCAAGT | 10533 |
| rs534787215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11448131 | CATCTTCTCACCTAA[C/T]CACAGATACCAGAAA | 10533 |
| rs534788409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312796 | AGAGAATGGTAACTG[G/T]TTGGAAGTTGTGCTT | 10533 |
| rs534789721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529193 | TCCTGGGGCACCTCC[A/C]AAGCCAGCCAGGTTG | 10533 |
| rs534810165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361439 | ACAGGTGTGTGCCAC[C/T]ATGCCCAGCTAATTT | 10533 |
| rs534814253 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395632 | ACAATTTTAAACCCA[A/G]CAGATAATACCGTTC | 10533 |
| rs534832858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486068 | AAGTAGTTTTTTCCA[A/G]TTCTGTGAAGAAGGT | 10533 |
| rs534840010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395591 | AAATAACTTCTTTAG[C/T]GTGCTGAAGGAAAGA | 10533 |
| rs534854156 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11448666 | GCAAAGCTGGTTGTT[A/G]TTGAACAAATTGCTG | 10533 |
| rs534854206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415243 | GTACACCTGTGCAGA[A/C]TACTTACCATAAATG | 10533 |
| rs534861811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528603 | AGGCTGAGGCAGGAA[G/T]ATCCACAAGGTCAGG | 10533 |
| rs534864622 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382540 | TTTCTACTTATTGTC[C/T]TGCAGAACTTTCTAA | 10533 |
| rs534865297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11404986 | TATCACATATTTTCT[A/G]GATTCTTAAGAATAT | 10533 |
| rs534875717 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436212 | TCACATGATAGCATA[A/G]TCAAATAAGATGCCC | 10533 |
| rs534884399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376700 | CAGAGCAGAGGGACC[C/T]TGGAGTGCAAGGAAT | 10533 |
| rs534891296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453624 | CGACATCATTTAGCT[C/T]TCTTATGAGTCATCC | 10533 |
| rs534911440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496172 | TTTAACTAAAAAAAA[A/C]ATCCACAGAGAAAGG | 10533 |
| rs534920455 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412250 | ATCTGATGAGTTCCA[G/T]TTATTTGATTCTTTT | 10533 |
| rs534921153 | in-del | -/ATA/ATAATA | 0.00795819 | 0.0626103 | intron-variant | ATG7 | GRCh38.p7 | 3:11349541 | CAAAACACTGTCTAT[-/ATA/ATAATA]ATAATAATAATAATA | 10533 |
| rs534928849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504885 | TTATGTTGAAATGGT[A/G]GAAAGATAGGGAGGC | 10533 |
| rs534936096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534562 | CGTCCTTCATGCCGG[A/G]TGGCTACGTGCCGCC | 10533 |
| rs534937412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541510 | GGTCTCCGATGGTCC[A/G]GCCCAGTGGCAGAGG | 10533 |
| rs534937440 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440481 | AGGCGCCCGCCACTA[C/T]GCCCGGCTAATTTTT | 10533 |
| rs534938252 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11540417 | CATCGGGTTGTTATA[A/T]CTTATTGAACTGTAA | 10533 |
| rs534943165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291864 | GTTTCCTAGGAACAT[C/G]AGCCATGCAGAAGAT | 10533 |
| rs534956129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406838 | CACCCCCATGATTCA[A/G]TCATCTCCCACTGGG | 10533 |
| rs534970364 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11474590 | GGGTGACAGAGTAAG[A/C]CCCTATCTCCCCATC | 10533 |
| rs534982826 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557268 | TAATAACAGTATAAA[A/G]TCAGAGGAATGTATA | 10533 |
| rs534990780 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11319462 | CTCATGTGTAGGATG[C/G]AGAAATGTTGGAATC | 10533 |
| rs534994405 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468346 | GCCAGCCCGCCACTT[C/T]CCTGGAAGAACTGAT | 10533 |
| rs535000955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429097 | CATCAAATTTTAGAT[C/T]AGAGATGGTAAACTG | 10533 |
| rs535010898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552478 | ACACAGTAGAGCCTG[C/T]AGATCCCAGCCCCCA | 10533 |
| rs535043552 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11428268 | TCAATGAATAGATGG[C/G]CAGGCCCAATACTGG | 10533 |
| rs535046556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382913 | CGTATATTTGCTGTC[A/G]TCCTCCAATCCCTCC | 10533 |
| rs535047679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11398344 | ATTAAACAAGTTTCA[A/G]CGAATTTCAGAGTGA | 10533 |
| rs535063562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11303370 | CCTATGTGAAGCTGA[A/G]AAAAAAAAAGAATTT | 10533 |
| rs535071271 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442415 | TTGGAAACTAAATAC[A/C]AACGAACCAAATGGA | 10533 |
| rs535084896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11392188 | GGGGTTGAGAGTTTA[A/G]AAGCTTTTTCTCAAA | 10533 |
| rs535090488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511878 | GCCAGCAGGGCTGGC[C/T]GGCTGCTCCGAATGC | 10533 |
| rs535098565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295365 | TCTTTCATTCATTCA[A/G]AATTGGATTTCTGTT | 10533 |
| rs535104469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521784 | GTCTCGATCTCCTGA[C/T]CTTGTGATCCGCCTG | 10533 |
| rs535105291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384912 | CATGCCATGGCACTA[C/T]AGCCTGGGCGACAGA | 10533 |
| rs535127203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347509 | TATACTTAATTATTC[A/G]TTAAGGGAAATCAAG | 10533 |
| rs535133998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431240 | AACCTTGTCTCTACT[A/G]AAAATACAAAATTAG | 10533 |
| rs535137957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443098 | TGAAATTGACTCCTC[A/C]AAAGGACAGCTGAAC | 10533 |
| rs535165020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403668 | GTTCCTTTTTCCTCA[C/T]ATTGCTTTAGAAATT | 10533 |
| rs535199195 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286691 | GCAGCCTTAATCTCC[C/G]AGGCTTAAGCGATCC | 10533 |
| rs535199884 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11397951 | TAGCTGAGCATGGTG[C/G]CACATGCCTGTAGTC | 10533 |
| rs535210741 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11390392 | ACAATATCTGCTGTC[-/T]TTGCCTAATCACTCA | 10533 |
| rs535212796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11439178 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 10533 |
| rs535214715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11431699 | TTTATTCATGTTGTA[A/G]CAAGGTACGCAATTG | 10533 |
| rs535216117 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438340 | TGAAGGCTATTTTCA[A/G]TATTTTGAAAAGTCA | 10533 |
| rs535218153 | in-del | -/AAAA | 0.00121803 | 0.0246481 | intron-variant | ATG7 | GRCh38.p7 | 3:11392472 | ATTAAAAAAACAAAC[-/AAAA]AAAACAAAACAAAAC | 10533 |
| rs535229519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11461419 | TTAGAATTTCCACGG[C/T]GTCTTTTCTTCCCTT | 10533 |
| rs535233599 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483661 | AGTGGAGCTTAATCT[A/G]TTTATCCTAGAGTAA | 10533 |
| rs535242441 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11483393 | TATCCACTGAGCTCC[A/C]AACACGCACAGATCT | 10533 |
| rs535243032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462241 | AAGGTTCAGGGCCCT[C/G]TCGTCACCATTGCTA | 10533 |
| rs535248669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498164 | ACACATATACATACA[C/T]ACATACATATGTACA | 10533 |
| rs535249251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370519 | AGTTTTTATTTATGC[A/G]AACTCCAAGCTTTAG | 10533 |
| rs535256634 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452811 | ATTGCAGATATTAGT[A/G]TTAAGACCTATTCTT | 10533 |
| rs535288702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543462 | GCTGAGTTTGGGGCA[A/G]TGGTTCCCTGAGAAG | 10533 |
| rs535304929 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489089 | TTTCAGAGCCTGTTA[C/T]TGGTCTATTCAGAAA | 10533 |
| rs535309742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500776 | GCTGGGACTACAGGC[A/G]TGCGCCACCACACCC | 10533 |
| rs535310429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11474469 | GCTGGGCATGGTGGT[A/G]TGCGCCTGTGGTCCC | 10533 |
| rs535310723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334045 | TGAGCCACCGCTCCC[A/G]GCCAGCTTCGGGAAT | 10533 |
| rs535333239 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462741 | CTCTCGCCACCCCCC[A/C/T]AGGGGCAGTCTTCCC | 10533 |
| rs535337108 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11518816 | AACTTTCACTGAATT[C/G]TAACAATTATTTCTG | 10533 |
| rs535358249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512136 | GCGAGGGCTCTGAGG[A/G]CTGCCAGCATGCTGT | 10533 |
| rs535362728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504303 | TGTATCAAGCCAAAC[C/T]GCTCATTGAATATGA | 10533 |
| rs535370951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11283888 | AGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 10533 |
| rs535374318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467932 | AATTCCTCCCCCAGT[A/G]TCATGGCTAAATTTA | 10533 |
| rs535386255 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11361744 | GTCAACTCACAGTGC[-/AA]AGTGGGTCAAGTGCG | 10533 |
| rs535388630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11549616 | TCCACTGTACGGATA[A/C]ACCACAATTTCTCTG | 10533 |
| rs535403619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525262 | TCTCGGACTCCTGAC[C/G]TCAGGTGATCTACCC | 10533 |
| rs535420499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532916 | AGGACCTGAGTCTTG[C/T]TATCTTTGCACCACC | 10533 |
| rs535428618 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287129 | CAAGGGATTAGGGAC[A/T]TTGAAAGGAATATGA | 10533 |
| rs535430280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317950 | TGCATAACTTTTCTT[C/T]GTATTAGTTTATCTG | 10533 |
| rs535453172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11478058 | GAGTAAATAGCACAG[C/T]ATGATTATCCTGCCT | 10533 |
| rs535462078 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11439643 | GCAGTGGGTGTGCAC[A/G]TGGTGCAGTAAGTTC | 10533 |
| rs535479407 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491239 | TCTTCCATCACTGAT[-/A]ACCCTTTCTTCCACT | 10533 |
| rs535498261 | snp | C/G | 0.00161225 | 0.0283465 | intron-variant | ATG7 | GRCh38.p7 | 3:11446476 | CTTGGCGTCATCATT[C/G]AAAATACTTTATTGT | 10533 |
| rs535507104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350160 | ATCTTTGCTTTAGAA[A/G]CATTGTTAATGTTTT | 10533 |
| rs535528064 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11451946 | CTTAAATGAGATTCT[A/G]TTTTTGTGAAGTGTT | 10533 |
| rs535529065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526098 | AATCTTGAATCATAA[A/T]CTTCATCAAGGGCCA | 10533 |
| rs535532276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11418831 | GCCTCAGGAAACTTA[C/G]AATTATGGTGGAAGG | 10533 |
| rs535551035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11324953 | AATGGACCACATATA[C/T]GGCAGTGGTTCCATA | 10533 |
| rs535554323 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11411289 | TTTTAAACTTGGTTG[G/T]TTGTTGTTGAGTTTT | 10533 |
| rs535562321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445745 | TTTCCAAAGCAGTTC[A/T]CTGACTTACATGAAT | 10533 |
| rs535565435 | snp | C/G | | | missense, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11340692 | CAGAAAGGAGGCATG[C/G]GACCAAGGATGGTGA | 10533 |
| rs535575210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331572 | GGTAATCAATAAATC[A/G]GTCATAACCCAATTT | 10533 |
| rs535587915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325462 | AGATCACCTGAGGTC[C/T]GGAGTTCGTGACCAG | 10533 |
| rs535594845 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372686 | TTTTCTGTATATTTT[A/T]CTGTACTAAGGGAAA | 10533 |
| rs535597015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11330774 | TCTGCCAGCAGAAGT[C/T]TTCACTGAAGAAACG | 10533 |
| rs535602919 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11326052 | GGAGCCTGAAGAAAT[-/C]CTTTGAGATGAAAGG | 10533 |
| rs535608457 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351501 | ACATAGAGGTCAAAG[-/A]AGATGAGGAGGAAGA | 10533 |
| rs535621560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379510 | TGTCTAGGGCCATTT[C/T]GGCCTTCCACAGTCC | 10533 |
| rs535622004 | in-del | -/T | 0.0236746 | 0.106192 | intron-variant | ATG7 | GRCh38.p7 | 3:11275516 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs535624110 | in-del | -/TA | 0.0185938 | 0.0946107 | intron-variant | ATG7 | GRCh38.p7 | 3:11381560 | TAACTGGGCGTTCCT[-/TA]TATACTTTAAAAGAG | 10533 |
| rs535643651 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11518995 | TTAAAAAAAAAATCT[-/TA]TATATAAGTAAATAT | 10533 |
| rs535644096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464866 | TTGGCCCCTTTACTA[C/T]AAAATGGAAATAGCA | 10533 |
| rs535644170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471494 | AAAAACATTTAAAAA[A/T]TTTTTACTGTCTCCA | 10533 |
| rs535647357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287615 | CTGATGCAGTCTTTC[C/T]GGAACGTTATGAGCC | 10533 |
| rs535653490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305525 | GTCTGAATGTAGAAG[G/T]CCTAGTTTACCAACT | 10533 |
| rs535658394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508048 | TAGGATAAACAACAG[C/T]CTCTACCACAGCTTG | 10533 |
| rs535660919 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11438276 | CCACCCATCCTCCAT[-/C]CCAGGGTCCCCAATG | 10533 |
| rs535665734 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11372820 | TGTGTGTGTGTGCGC[A/G]CGTGTGCGTGTGTGT | 10533 |
| rs535674002 | in-del | -/G | 0.000747987 | 0.0193244 | intron-variant | ATG7 | GRCh38.p7 | 3:11307111 | CCTGTGGTCCTGGCA[-/G]GTGCAGTGTTTGTGA | 10533 |
| rs535679169 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11521213 | GCCATAGGCAGCCAT[G/T]AGTTGAGAAGGCCAG | 10533 |
| rs535698337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345411 | AGGACTCTGTCTCAA[A/T]AATAAAATAAAAGAA | 10533 |
| rs535701686 | in-del | -/TTTTTA | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11551600 | TAATTTTTTTTAAAG[-/TTTTTA]TTTTTATAGAGAGAG | 10533 |
| rs535704837 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11363603 | CTATTATTATTAGTC[A/G]CAGTTTTGATGGGGA | 10533 |
| rs535714394 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11555082 | TTGCTATTGACCTGG[C/G]ACTTGGTCCTCCATG | 10533 |
| rs535733936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344070 | GATGTTTTTTCCTTT[A/G]GAGATATTTTCTCCC | 10533 |
| rs535755821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11519812 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 10533 |
| rs535759985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405866 | CTTAAGACATCCACC[A/G]CCTTGGCCTCCCAAA | 10533 |
| rs535776448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352850 | TGAAGGAATTGATCA[G/T]AAGAGGTCTTGAGGA | 10533 |
| rs535779419 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11385535 | CAATAGCCACTGTCT[C/T]CAAGGAACACTGCCT | 10533 |
| rs535798763 | in-del | -/TTTCTTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295785 | TCTTTTCTTTCTTTC[-/TTTCTTTT]TTTTTTTTTTTGAGA | 10533 |
| rs535809479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321075 | GTAGGGTGCAGATGC[A/G]TAATGTCTGGGAATG | 10533 |
| rs535811004 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11435626 | CCTCAGCTCCCACAC[A/G]TAGCCAAGACTGCCA | 10533 |
| rs535819200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490254 | GTCTCTTTTGATCTT[G/T]GTTGGTTTAAAGTCT | 10533 |
| rs535827528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455238 | TCATGAAGCAAGTTA[C/T]TGATTTTAAGTAGAA | 10533 |
| rs535837967 | in-del | -/ACAA | 0.477937 | 0.102688 | intron-variant | ATG7 | GRCh38.p7 | 3:11478995 | ATATTTACAACACAC[-/ACAA]ACACACACACACACA | 10533 |
| rs535842309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367364 | AAAGAAGACCAGTGA[A/G]GTTTACTGGGCTCAT | 10533 |
| rs535844768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407822 | CTTAGGCTGTACACA[A/G]CACAGGGACCCTGGG | 10533 |
| rs535845903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11311059 | GTTTGCATTTAATGA[A/G]AAAAATAACATTAGC | 10533 |
| rs535860149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370446 | ACACTCTCCATTTTG[A/G]CATTGAACTTGATTA | 10533 |
| rs535874661 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11314380 | GAGCTCTCTTGGAGC[C/T]GTTCAGGGAGCAGCC | 10533 |
| rs535878429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465065 | AATTTTTTTTCTTAT[C/G]AAATCAATCTCTAAA | 10533 |
| rs535887107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449581 | TTCTAGAGAGAATGA[C/T]TTTCCCGACCCTTCC | 10533 |
| rs535893083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536212 | GTTTTCAGTAGATTG[A/G]GAGGCTCATTAGGGG | 10533 |
| rs535900348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501344 | TATCAGAAAACCTGA[C/G]AAAAGTGCCTAATAT | 10533 |
| rs535907224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11373290 | GTTAATTTAACATGA[A/G]CTAAATTAGGTGGTG | 10533 |
| rs535912873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454634 | TGAGGCCACATTTCC[C/G]TTTTAGCTTGAGTAA | 10533 |
| rs535917157 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512816 | CAGCCTGCTTTTATT[C/G]TCTTACCTGGCCCCA | 10533 |
| rs535921995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11504258 | AATGCTTTCAAACAA[C/T]AAAGGGAAATTATAT | 10533 |
| rs535947279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494253 | GAAAACAGGAATTAG[A/G]GAGGGGTAAGGAAGA | 10533 |
| rs535947617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274341 | AGATAGCAACGGTAT[A/G]GCATGAAGCTATTGC | 10533 |
| rs535955290 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11489244 | CATTTAAGTCTGCAG[A/G]GGTTACTGCTGTCTT | 10533 |
| rs535958406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494855 | AAGGTGAGTGGATCA[C/G]GAGGTCAGGAGTTCG | 10533 |
| rs535966933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541125 | CAGGATGGTCTCGAT[A/C]TCCTGACTTCGTGAT | 10533 |
| rs535967375 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414530 | TCCCAATCAGAATAC[C/T]CTTTATTTCTTTTTC | 10533 |
| rs535971250 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292257 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTGG | 10533 |
| rs535980088 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430752 | GTGAGCTCTAATGCA[A/G]TAAAAAATGTTTTAG | 10533 |
| rs535986709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273412 | AGCTACTCGGTAATC[C/T]TAGCTCACTGTTCCT | 10533 |
| rs536015597 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11425812 | CCTTGTGCCCCTTAC[A/G]GTCTCTCTGTGGGTA | 10533 |
| rs536039257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11297071 | TTAAAAAATATATCC[C/T]ATTTGGCCAGGTGCA | 10533 |
| rs536061773 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304768 | TTTTTACTAGGTTAG[C/T]ATACGCATTATCGCA | 10533 |
| rs536062130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11513594 | GGCCCACAAGTGTGG[C/T]GTGCAGCCCCAGTTC | 10533 |
| rs536074303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297714 | TAGGCACTGTGGGAG[A/G]TGGGGAGAAGCATAT | 10533 |
| rs536076972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11433177 | CACACCAGCTACTTA[C/T]AATGCTGAGGCAGGA | 10533 |
| rs536079494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348935 | GTTTTTACAGAGTGC[C/T]GATTGGTGCGTTTAC | 10533 |
| rs536086177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11437442 | ATCCATAGAAGACAT[C/G]GCAGATAAAGGGGTT | 10533 |
| rs536097857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11450154 | TTAAATCTTCACAAT[C/T]ACTTTATTTAACAGA | 10533 |
| rs536123294 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345180 | GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTCAG | 10533 |
| rs536140175 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11277838 | GAACAGGGCATATTT[C/T]AGTCCTTATCTCAAC | 10533 |
| rs536170371 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440722 | GACTTTCGCTCTTGT[C/T]GCCCAGGCTGGAGTG | 10533 |
| rs536171147 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350862 | GAGGCTGAAGTGGGA[G/T]GAGATCGCTTAAGGC | 10533 |
| rs536173787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443986 | TAACTAGAAACAGTA[A/G]ACTTTTCCTGTACAA | 10533 |
| rs536175773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11295817 | TTGAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 10533 |
| rs536180553 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451081 | TTTATTTGACCTTAA[C/T]GAAATGAAAAAGACA | 10533 |
| rs536182363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393123 | CAGGACCAGAGTGCC[A/G]CTGCAGAAAGTGTTA | 10533 |
| rs536190215 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11484832 | GTTTACTGAGAATGA[A/T]GATTTCCAATTTCAT | 10533 |
| rs536190535 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11445684 | GAACTTACAAGTTTC[-/A]AAAAAAAGAAAATAT | 10533 |
| rs536203566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11399734 | CATAAGCCACCATGC[C/T]CAGCTAATTTTTTAT | 10533 |
| rs536211617 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395907 | GTCACACCACTATAC[A/T]CCAGCCTGGGCGACA | 10533 |
| rs536215619 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270550 | GGCTGTTTATTTCAC[A/C]TGGGTGCAGGTGGGC | 10533 |
| rs536225546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277926 | AATGCATTCCTTTCC[A/C]AGGGTCTTAATTATT | 10533 |
| rs536225944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492186 | GTTTTTAAAGCCCAT[C/T]GGAAAGGCGCAGTAT | 10533 |
| rs536232658 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399042 | ACATGTATCTTAGCA[C/T]TGAATTTTTAAAAAT | 10533 |
| rs536234770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362234 | TCTCTTTGGTTGAAC[C/G]AGCAAAGGCTTGTGC | 10533 |
| rs536241244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469270 | GCCTGACCAACATGG[A/G]GAAACCCCATCTCTA | 10533 |
| rs536249988 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501708 | ATACTTTTTATTTTT[A/T]AGACAGAGTCTCCCT | 10533 |
| rs536253613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343532 | TATTTTTCTCAGTTT[A/G]TCTAAGGTGTCTTTA | 10533 |
| rs536259618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285663 | TCACCCTGTAATCAC[A/C]ATTCTAACTTCTGTC | 10533 |
| rs536265000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11377998 | TTCATATGTTTATGA[C/T]GAGGCTATCTAACTT | 10533 |
| rs536295993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370114 | CATTAGCACAGTTCT[A/G]GGCACATAAGAGACC | 10533 |
| rs536299077 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11542215 | CTGCTTCTAACCAGT[G/T]CTTGGACAAGCCCTT | 10533 |
| rs536326273 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11402060 | ATGCAACTGAGACAG[G/T]AATAATAACAGGGTG | 10533 |
| rs536333987 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520107 | ACATGAATTTGTTTA[A/G]TTTTCACCAAGGTCT | 10533 |
| rs536336654 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11334660 | ATGGGGGAGGTGGTG[A/T]CAAAATCTCTTCCAA | 10533 |
| rs536348222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11497093 | TCAACTCAAGTGATC[C/T]GCTTGCCTCGGCCTC | 10533 |
| rs536348475 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11330854 | GGATGGGAAAGGGGA[-/G]GGAGGAAATATATGT | 10533 |
| rs536350180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277296 | TGCATAGCTTTTCAC[A/G]TAAGGCTCTTCATGA | 10533 |
| rs536355937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407438 | ACAGTTGTCAGTGGA[C/T]CTATCATTCTGAGGT | 10533 |
| rs536360601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498084 | ATTAGAATTCAACCC[C/G]AGTTAAATCCTGACT | 10533 |
| rs536371423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335592 | CACTTAATTCTGCCA[A/G]CCACTCTGCAGAGAG | 10533 |
| rs536379304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468574 | TTCATTAGCCCTCTC[C/G]ATCCCCACAGAGAGG | 10533 |
| rs536384279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11284533 | ATGGTTTAAAGATAG[A/G]GGTTTTGTTCTACTT | 10533 |
| rs536385302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11383531 | CTCACTGCAACCTCC[A/G]CCTGCCTCCCAGGTT | 10533 |
| rs536390340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276700 | AACCCAGTCCTACTT[A/T]GTATTATCTCTCTGG | 10533 |
| rs536408318 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11454442 | ACGGCATGAGTCTGG[A/G]CTGGGGCAGCCTTCT | 10533 |
| rs536412142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315787 | GCTGGAGCGCAGTGG[C/T]GCAATCTTGGCTTAC | 10533 |
| rs536416659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11396467 | GTGGGTAACTCTAAA[C/T]GAACATTTGAACATT | 10533 |
| rs536417679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11493456 | GAAAGAATGACTCAG[A/G]AGAGAGCAGGCAAAC | 10533 |
| rs536422967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523038 | CCGATGAAATAGCCT[G/T]TACTTTATAAAGTAT | 10533 |
| rs536427238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308161 | AGTATGTCAGTAGCA[A/G]GAACTTACTTCTGCT | 10533 |
| rs536431067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300644 | GAGGAGAAAGAGAAT[A/G]AAGATAGTCTCCAAC | 10533 |
| rs536447079 | in-del | -/TT/TTT | 0.00795939 | 0.0626292 | intron-variant | ATG7 | GRCh38.p7 | 3:11459498 | AACAGGAGCCAAGTG[-/TT/TTT]TTTTTTTTTTTTTAA | 10533 |
| rs536450755 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | ATG7 | GRCh38.p7 | 3:11309068 | ACATTTGCAGTAAGT[A/G]AATGGGCTCTCGGTT | 10533 |
| rs536455776 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322952 | AAAAATTTAAAAATT[A/C]GCTAGGTGTGGTGGC | 10533 |
| rs536466399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292061 | TATCACTGCAAGAGC[C/T]GAGGTGTGAGATGAT | 10533 |
| rs536467961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301312 | AAAAAGGCTACAGTG[C/T]TTTTTCTGCTTTATT | 10533 |
| rs536477521 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11305969 | GACAACATTAGTAGG[C/T]TACTAATGAAATGAA | 10533 |
| rs536487674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11427955 | AGTGAGATTAAATCA[A/G]TCTTTTCCCCTTAGT | 10533 |
| rs536496031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341131 | CAATGGCGCAATCTC[C/T]GCTCACTGCAACCTC | 10533 |
| rs536498404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11371716 | CATGAAAACATGGCT[C/T]CTTGATAGCATCACC | 10533 |
| rs536511949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11363757 | CAGGCAGCAGAAAAT[A/C]GAATTTTTGAAAGAT | 10533 |
| rs536519213 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317799 | GGTTTCACCATATTG[G/T]CCAGGCTAGTCTCAA | 10533 |
| rs536534900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492393 | AGATGAACCCAGTAC[C/T]TCAGATGGAAATGCA | 10533 |
| rs536536983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401825 | AATATTTTTTCTTTG[C/G]TCTAGGGTCTCAACT | 10533 |
| rs536537762 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345810 | TTATTTTACTGTCTT[C/T]TTCTAGGTTCTAGAA | 10533 |
| rs536546084 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272054 | CACACCTGCCACCCT[C/G]ATGGCCCCTGTGCTG | 10533 |
| rs536554636 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11493053 | CCTTTTTGGGTACCC[A/C/T]CACTTGGTGGATCCC | 10533 |
| rs536569922 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11401437 | AATAGAAAGTTGTAT[A/C]TTCTAAAAATTCATT | 10533 |
| rs536592526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481644 | TTCCTGGGTTGGGCC[G/T]TGGACTTAATGTCAG | 10533 |
| rs536595094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338809 | TAGCTTTCAAGGATA[A/G]TTGGTCCTATGGTTT | 10533 |
| rs536597269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402484 | AGGGGCTGATAAGAC[C/T]CTGAAAAACCAGGGT | 10533 |
| rs536600398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335895 | GTAGAGTCGGGGTTT[C/T]ACTGTGTTGGCCAGG | 10533 |
| rs536601618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329282 | ATTGGTTAAGCTCCT[A/G]CTTTGTGGCTGATAC | 10533 |
| rs536617142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289273 | AGTGACACATGAATA[A/G]CTCTGTCTATGACTC | 10533 |
| rs536621138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286204 | CTTCATTAAAATGCT[A/G]TATTAATGACCAGAT | 10533 |
| rs536622392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387154 | CTGAGATACATGCAG[A/C]CTTTTCTGGGCTCAC | 10533 |
| rs536623772 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11480850 | GCCTCCAGTCCTGGC[C/T]GGCTGGGCCTCTCTT | 10533 |
| rs536624218 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11281499 | AAAATCAGGCCGGGT[A/G]TGGTGGCTCACGCCT | 10533 |
| rs536629827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384093 | CCTTCTCTAAAAGGA[A/G]TAAAGCTAGGCAGCT | 10533 |
| rs536630065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380118 | CATTTGACCGCAGCC[A/T]CACCAGCTGGAGCCC | 10533 |
| rs536638876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465606 | AAAAAATAATAATAA[A/T]AAATAAAAATTAGCT | 10533 |
| rs536646468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472565 | GAAAAATTAGAAAAC[C/T]GGTGAGTTTATCAAA | 10533 |
| rs536650425 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272333 | CTGCTCCTTTGCGCA[A/C]GCGCGCCGCTTCCCA | 10533 |
| rs536662390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373551 | AGTTCCAGGGGCTTC[G/T]TCTGATGAGGCAAGT | 10533 |
| rs536682405 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11528544 | ATAGAAAGTTAAAAT[A/G]GTTTGGGCGCAGTGA | 10533 |
| rs536683071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418952 | TATCGCAAGAACAGC[A/G]TGGGAAACTGCCCCT | 10533 |
| rs536698518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293050 | GATACTATTAAGCAA[A/G]CTAGGAAATACAGAG | 10533 |
| rs536709598 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11501940 | GTTGATCCCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10533 |
| rs536735015 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11429831 | TGTGCGCCTGTAGTC[C/G]CAGCTACTCTGGGAT | 10533 |
| rs536736745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517117 | AAGTGAAAGAAGCCA[A/G]TCTGAAAAAGGCAGC | 10533 |
| rs536739817 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11310833 | GAGAGGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10533 |
| rs536745719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511484 | AATCCCTGAGCTAGA[C/T]ATAAAGACTCTCCAT | 10533 |
| rs536748268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550647 | AAGTGATCCTCCCGC[C/T]TCAGCCTCCCAAAGT | 10533 |
| rs536753884 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11547504 | ACAAGTTTTTATGTG[A/G]ACACGTTGTCATTTC | 10533 |
| rs536758579 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11477765 | AACCAGGACTCAGGG[C/T]TAGGAACTGGGAATC | 10533 |
| rs536765167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430394 | CATACTTGATTCTCA[A/G]TGCGTTTACAGGTGG | 10533 |
| rs536765267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422711 | TCAGCTTTTGACATG[A/C]CTTCCTCACTATGCT | 10533 |
| rs536769907 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11335551 | TGTGTGTCTGACAAG[C/G]TGCCAGGCACCTTCC | 10533 |
| rs536774436 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278044 | TGTATTCTGCCTGAC[C/G]CTGTAGGCAGTCAGA | 10533 |
| rs536790796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386589 | TTTGCATACAGCTTC[C/T]CAGTGGCAAATATTA | 10533 |
| rs536795633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390771 | CTGCAAGTTAAAGTA[C/T]TGCAAGGCTTAAAAT | 10533 |
| rs536798412 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11402794 | TTTTTTAACAATTTT[C/T]TTAATGGAGTCAGGG | 10533 |
| rs536806495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11534082 | AGCCTCCTCCTCCCC[A/C]CCCAGGGGAAAGCTG | 10533 |
| rs536816160 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11491019 | TCTGAATGTTGGCCT[A/G/T]CCTTGCTAGATTGGG | 10533 |
| rs536817235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530580 | GGTGAAATGAATCCC[C/T]TCCTCTGAGACCAAC | 10533 |
| rs536820774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450832 | CTCCCTTGTCACTTT[C/G]CCTGAAATGAGAAAC | 10533 |
| rs536827231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11488538 | GCACTGCCCCGGGCC[A/G]CAGCGCAGCGGCGCC | 10533 |
| rs536829722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410298 | ATTTGTACCTAGGTA[C/T]TTTTGGGTGTTGCTA | 10533 |
| rs536836913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457460 | TAACTGGAGTCTCTT[C/T]TTGGGGCATAATTGA | 10533 |
| rs536854824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319470 | TAGGATGGAGAAATG[C/T]TGGAATCCCTCTGAG | 10533 |
| rs536890034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451299 | TCACTGAAACCTCGG[C/T]CTCCTGGGTACAAGT | 10533 |
| rs536900317 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11502213 | ATTCTTTTTTTTTTT[A/T]ATTTTAATTTATTTT | 10533 |
| rs536902760 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406989 | ACCAATCATGTCTTC[C/T]CAACAGTCCCCCAAA | 10533 |
| rs536936038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329769 | ACATTATATCACCAC[A/G]GTTCATTTGTCAAAA | 10533 |
| rs536946810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275205 | TGAATTTGCTGTGTG[A/G]AATTGAGCAGTAACA | 10533 |
| rs536956526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417269 | ACTTCTGATAGAGCA[G/T]TATTGAAGTCTACAG | 10533 |
| rs536957127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495727 | ATCATTCTAACAGCC[A/G]TGGATATCACCAAGT | 10533 |
| rs536962355 | in-del | -/TTTTTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507631 | TAAAGTTATGGGTGT[-/TTTTTG]TTTTTGTTTTTGTTT | 10533 |
| rs536968797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537044 | CCCCTCTCCGCGGAC[C/G]CTCTGATGGCAGACC | 10533 |
| rs536984140 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11274606 | AGCACTAGCCACATC[A/G]TGAAGGGCCCTGTGG | 10533 |
| rs536986139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11282116 | AGGAGGCACACTGCC[C/T]TCCATCTTCCTGGCA | 10533 |
| rs536995078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500118 | AGATGACCTTTTAAT[C/T]CCCTTCCAGGGCTAA | 10533 |
| rs537013413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485697 | ATTTAAGTCTTTAAT[C/T]CATCTTGAATTAATT | 10533 |
| rs537013970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521391 | AAAGATGAGGGAGGG[A/G]TATGTGGTGGTGGAG | 10533 |
| rs537020733 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11503646 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 10533 |
| rs537022113 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551147 | GGACATGGTCTTCTC[A/G]TTTCTGTACTCGTCG | 10533 |
| rs537025958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306226 | CAACCGTCAGGGGCT[G/T]GCCCAGCAGCAGTTT | 10533 |
| rs537026990 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456829 | ACACTGTATGTGTAC[A/C]CTTTTCTGAAAGTGC | 10533 |
| rs537027805 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557063 | GGTGACCACGCCCAC[A/G]TCACCTGGTCAGGTG | 10533 |
| rs537037609 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479293 | CTTTAGGTGAACTGA[A/G]TTTAAATTAAATGTT | 10533 |
| rs537039277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551261 | GGGGGCTTCTCACCG[C/G]TCTTCTGTTCGGAGG | 10533 |
| rs537052383 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309348 | TTTCATTGTTGCTAA[C/T]GCCTTTGTTAAATAC | 10533 |
| rs537052603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514689 | GCCTGATATGCATAG[C/G]ATACTTACATAGCTC | 10533 |
| rs537052675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11521743 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 10533 |
| rs537052952 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317030 | TATTTTTATTAGAGA[C/T]GGGGTTTCACCGTGT | 10533 |
| rs537054438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395278 | GAAAGTCTAACAGTC[A/G]TAATTGGAAATCTAG | 10533 |
| rs537055376 | in-del | -/TTGC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496341 | AGTGGGAGGTGGAGA[-/TTGC]TTGCATAAACTCATT | 10533 |
| rs537057995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465993 | TTTGTGTCTTTCACA[A/G]AGGGCAGTAAAATTT | 10533 |
| rs537058033 | in-del | -/A | 0.170084 | 0.236883 | intron-variant | ATG7 | GRCh38.p7 | 3:11281775 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs537061907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288500 | TATCTCTCTCTTTGT[A/C]TTCTTGCCATTGGGT | 10533 |
| rs537065854 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279758 | GGCTTAAGGGTTTCT[A/G]TAGGAAACACTGTTG | 10533 |
| rs537066224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508825 | CCAACACTTCACAAG[G/T]GTTGGCTTCTGAAGT | 10533 |
| rs537069685 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11454899 | ATAGGATAGCACTAC[G/T]ATAGAGAGGACAAAC | 10533 |
| rs537081665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544594 | ACCCCAGCTGCTCCC[A/G]CCTGGGGATGCTCAC | 10533 |
| rs537093355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442361 | TGCCTACTCCACAAA[A/G]TTGATGTGCTTTGAA | 10533 |
| rs537100956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11296790 | CCCATCTTCCCCCAC[C/T]CCTTACCCATCCTTT | 10533 |
| rs537127722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11344762 | GTAGTTGCAGCTGCT[C/T]GGGAGCTGAGGTGGA | 10533 |
| rs537132898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399854 | GCTGGGATTACACGT[A/G]AGCCACAGTGCCTGG | 10533 |
| rs537136740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520499 | CTGATGGTGGCTGCC[A/G]TGCCAGGCACCATAC | 10533 |
| rs537152211 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556148 | CAAACCTTTTTTTTT[C/T]TTCTTCCAGGAAAAA | 10533 |
| rs537163246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433070 | GCTAAGTTGGGAGGA[C/T]TGCTTGGGTCTGGGA | 10533 |
| rs537173198 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313782 | ATGTTTGTCTTTTAA[C/T]AGATATGGGGTTTTG | 10533 |
| rs537179188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513541 | GGCCGCTCCCAGTGC[A/G]GGGCCTGCCAAGCCC | 10533 |
| rs537179199 | in-del | -/TGATATTGCAT | 0.4973 | 0.0366419 | intron-variant | ATG7 | GRCh38.p7 | 3:11501538 | ATTATTAATAGATAA[-/TGATATTGCAT]TGATATTAATAGATA | 10533 |
| rs537186882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312441 | AATCCTTTCCCCTGG[A/G]TCTCCTACCCTGGTG | 10533 |
| rs537194029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11539790 | CTGAGCTTTGAGAAA[C/T]GTACTCGCTTGTGGA | 10533 |
| rs537206830 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11318723 | CCACTAGCCTCATTT[A/G]ATATTTCCCAAGATA | 10533 |
| rs537208381 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11422006 | TCAGTAAACTGTGCC[A/G]TAAACAGATGTGCTG | 10533 |
| rs537218465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318790 | GCCGCAGCTTCCCCC[A/C]TCTCTCTGCCTGCAG | 10533 |
| rs537224084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453155 | GGAATGTCCAGTTCA[A/G]TGTTGAGGGGGCTGA | 10533 |
| rs537241148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11368563 | TTGGGAGGCTGAGGT[A/G]GGAGAATTGCTTGAG | 10533 |
| rs537245153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546226 | ACCCAGGCTGGAGTG[C/T]AGTGGCGTAATCTCG | 10533 |
| rs537248611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453532 | AAGCTATTTAAAAGA[C/T]CCTAAAGTGCTGCAG | 10533 |
| rs537255788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311741 | TTGCTTTCCTTCTGC[C/T]GTTTTTTAGGACTCA | 10533 |
| rs537256751 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555623 | GAGCAGGCCAGGCCC[A/G]GAAAGGCCGAGCCTG | 10533 |
| rs537264272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510926 | TTCAAGAATGAAGCC[A/G]CGGACCCTCGCGGTG | 10533 |
| rs537284370 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433831 | CTTCCTTTCTGCAGA[G/T]TTGGGGATTAATGAA | 10533 |
| rs537291237 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404871 | GAGAAAGACCCGCCC[C/T]CATGATTCAGTTACC | 10533 |
| rs537291387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534493 | TCATGGAGGAGAGGA[C/T]ACCTCCCCAGAGCCA | 10533 |
| rs537294299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414136 | AGTGCCATCTTGGCT[C/T]ACTGTAACCTCCACC | 10533 |
| rs537295158 | in-del | -/TTTATTTATTTATTTATTTATTTA | 0.383053 | 0.211653 | intron-variant | ATG7 | GRCh38.p7 | 3:11462842 | CTCCTCTCAGATATT[-/TTTATTTATTTATTTATTTATTTA]TTTATTTATTTATTT | 10533 |
| rs537318681 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483258 | CAGTCTTGGCATCAC[-/A]AGAAGCTTGACGAGA | 10533 |
| rs537332166 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11325548 | TGGTGGCGCATGCCT[C/G]TAATCCCAGCTACTC | 10533 |
| rs537339961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515242 | CCACTTTTCAGTGTG[C/T]TCATGTCTCAACTGA | 10533 |
| rs537357029 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11428312 | GAAAGGGCTGCTGTT[C/T]GGAGAGGTGGAGCTA | 10533 |
| rs537357839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11340324 | GTCTTTTTTTTTTTT[C/T]CAGCAACTTCCAATA | 10533 |
| rs537367080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539582 | TGCTGGCGGGGGGTC[A/G]CCCACTTTCCACCTT | 10533 |
| rs537368663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428217 | AAATTCCTCCATAGG[C/T]TGCATATCCTCACCA | 10533 |
| rs537411908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523532 | AGAGTGATGGAAAAG[G/T]CTGTGCTGCCATTCC | 10533 |
| rs537420991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11536730 | CCGGGGCCGAGCAGC[A/G]AAGGACCACCCTGGT | 10533 |
| rs537426075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11308915 | GCTTTTCAGCTCCAC[A/G]CTTCACCTGAGAGTG | 10533 |
| rs537435239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442002 | AAGATGAGGTTTCAC[C/T]ATGTTGCCCAGGCTG | 10533 |
| rs537445702 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11515493 | ATTTTTAGTAGAGAC[-/G]GGGTTTTGCTGTGTT | 10533 |
| rs537450092 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330027 | TTATAGAATGTCCCT[C/T]AATTTGCATTTGTCT | 10533 |
| rs537454349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524281 | CAGCCACAATGGAGA[A/G]GCCCATTCCCACTCT | 10533 |
| rs537461939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473786 | ATTAAATCAAGACTT[C/T]ATTTTTAAATGTAAC | 10533 |
| rs537466247 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11480709 | GCTTTGCTCACAAGG[A/T]CTTGAAACCCAGGCT | 10533 |
| rs537489935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349939 | TTGACAGTTTTCTTT[C/T]TTTAAGGTCAACCAG | 10533 |
| rs537492888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438201 | CTTCTCTGGGTGTCA[C/T]CAGGGCATCCTGGTC | 10533 |
| rs537498418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434778 | TCGGATGGTATAATC[C/T]GCTTGGAGAAGTCTA | 10533 |
| rs537504419 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558030 | CCTCAGAGTTCTGGC[A/T]TAACACATAAAGTTG | 10533 |
| rs537513070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11368920 | AATGTGTATATGCCA[C/T]TCTTCTGAGCTTGGA | 10533 |
| rs537516084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450783 | GTGATATAGGTTCTA[C/G]CTTTCTTAGTTAAGA | 10533 |
| rs537537448 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11491454 | AGTTTGATCGTCAGA[A/C]GCCTTCTTCTCTCAA | 10533 |
| rs537554245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11353571 | GAGGTGGGGCCTGGT[A/G]GGAGGTGTTTGGGTC | 10533 |
| rs537576171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11364927 | ATGGGAGGAAATCAC[A/G]AACGAGAAGCATTGC | 10533 |
| rs537578173 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406620 | CAAGACTGGGCAGTT[C/G/T]ACAAAAGAAGGAGGT | 10533 |
| rs537591459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488491 | CTGCAGCTGGGGCCC[A/G]CGGGTGTCAGCGCCG | 10533 |
| rs537602634 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11388162 | ATGGCTTTGGGAACT[C/G]ACCATCTACCTCTGG | 10533 |
| rs537620629 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297631 | GAAATAATAAAATAT[-/A]ATATCATGGCACAAA | 10533 |
| rs537645214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11467276 | GAGTTTAAATTCACT[A/G]CTTATTAGCTGGGAA | 10533 |
| rs537650047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11548922 | TAAGCCGTAGGAATC[A/G]TGGCTGTTGCCAGAT | 10533 |
| rs537656703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286481 | AGTCATAGAAGTTTG[G/T]GTTATTTCTTGCTTT | 10533 |
| rs537659641 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11375800 | CCCGACCTTGTGATC[A/C/T]GGCCGCCTCAGCTTC | 10533 |
| rs537661194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11460729 | TCAAGGACATATAAA[C/T]TTTGACAAATAATAT | 10533 |
| rs537661369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283274 | AGGCAGAGGAAATTT[G/T]CATAGTGAGCATGGG | 10533 |
| rs537662813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464183 | TTGAGACTAGCCTGG[A/G]CAACATGGTGAAACC | 10533 |
| rs537669533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503670 | CTGAGGCAGGAGAAT[C/T]GCCGGAACCCAGGAG | 10533 |
| rs537674650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542945 | GCATCTTTGTAGGGG[A/G]AGTGGGGAGGATTTG | 10533 |
| rs537674920 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472418 | CATCCACCAGTGACC[C/T]TGTCACTATGGTAGA | 10533 |
| rs537692442 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11381863 | GCATTTACTTACTTG[A/G]CTACCTTCTTTATTT | 10533 |
| rs537703906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430558 | AAACGATTCAACTAG[A/G]TAATTATATGTGACA | 10533 |
| rs537708133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438819 | GTGGAGAATCTCTGG[C/G]CTGTGGCGCTGCTGA | 10533 |
| rs537715092 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557625 | AGCAGTAAGTATATC[C/T]AGGACTGTAACTGAC | 10533 |
| rs537727578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347450 | AGTCATTTTTTGGAG[G/T]AGTTCATTCAGGCTT | 10533 |
| rs537728230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11494666 | AATAGATCATCTCTT[A/G]ATGGAACACAGATAT | 10533 |
| rs537737039 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332485 | TATGAAGATAGATAA[A/G]TTATAGATTGTTCTC | 10533 |
| rs537750023 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485379 | CTTCGCCCACTTTTC[A/G]ATGGGGTTGTTTGTT | 10533 |
| rs537751786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11552376 | TTTTTTAAAATGTGC[C/T]AGTTTACTATGATCT | 10533 |
| rs537760112 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11554005 | AGGGAGCCCTGGGTG[C/T]CAGGGGCCCTGGGAC | 10533 |
| rs537773752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431138 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10533 |
| rs537777260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11511854 | GTGCTAAGTCCCCCA[C/T]TGCCTGGGGCCAGCA | 10533 |
| rs537779216 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303947 | AAAAAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 10533 |
| rs537788710 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312582 | CTGTCCACAAAGTGA[A/G]CTGCCTGGTGTCTGG | 10533 |
| rs537796523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11303223 | CTCCACTCAGATTCT[A/G]CTGAGGAGAACTCGT | 10533 |
| rs537796626 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11290111 | TCCCCTCCAATTAGT[G/T]TTCCAGCTCACTTTT | 10533 |
| rs537801436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483037 | GTTTTTCCACCTATA[A/C]CCACCTCTAAGTCCC | 10533 |
| rs537814124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316780 | CTTAGCCATACAGGA[G/T]ACTATGAATTAAAAA | 10533 |
| rs537826749 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11547091 | ATTTGCGTGACAGGC[A/G]GTGAATGGAAGAGTG | 10533 |
| rs537833829 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519704 | AGCTGGGACCACAGG[C/T]GCCCGTCACCGCGCC | 10533 |
| rs537854102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397858 | GAGCCTGAGGTGGGC[A/G]GATCACCTGAGGTCA | 10533 |
| rs537856637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11451908 | ACACACACAGACACA[C/T]ACACACACACATATA | 10533 |
| rs537861857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476929 | ACAGATTATGGCCCT[C/T]TTTCCCTTTAAGCAA | 10533 |
| rs537891666 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396927 | AGATAAGTCAAGGAT[A/G]TATGTTATAACTGAT | 10533 |
| rs537892006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532226 | GCATTTATTGATGCA[A/G]TGCACCACATGAGAT | 10533 |
| rs537894895 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11445057 | AAGTCAAACAATAGA[G/T]GCTGGCGAGGTTGTG | 10533 |
| rs537914758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364866 | TGGGATTTCAATGGG[A/G]GAGCTTTCTGACCAC | 10533 |
| rs537940602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330261 | GGAGGGGAAGGTTTA[A/C]ATTTTGCTTCTGAAG | 10533 |
| rs537948442 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11417456 | ACATTATTTGCTTTG[A/T]AGTCTGTTCTATCTG | 10533 |
| rs537949665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357361 | ATATAAAAAATCCCA[A/G]TTCAGGGGAACTCAG | 10533 |
| rs537988269 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11543846 | CCTCTGGGGACGGGA[G/T]GGGGAGGACCCATTT | 10533 |
| rs537996685 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372231 | GATTCTTCTAGGCTC[-/TG]TGATTCCCAGGTGGG | 10533 |
| rs538021926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392316 | AATCCAAGACAGTGC[G/T]GTTTTGAAAATGCAA | 10533 |
| rs538025228 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529694 | ATAATTGAGGCTTCA[C/T]CTGGTTAGCAACGTC | 10533 |
| rs538031790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295219 | ACTGAGGCAGTGGGG[A/G]ATTTTAGGGACAGTG | 10533 |
| rs538044270 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11555004 | GGAGTGGCCAGTGTT[C/T]GGCGTTGCTCGGGAT | 10533 |
| rs538058459 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339936 | AGTATAGAAGCATTT[A/C]CAAAGTCTGTTTAGC | 10533 |
| rs538064412 | in-del | -/G | 0.00160514 | 0.0282841 | intron-variant | ATG7 | GRCh38.p7 | 3:11330827 | TTCCAGATGAAGATC[-/G]GGATTGGAGTGGGAT | 10533 |
| rs538070558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296126 | GGACATTCTCTAGGA[C/G]TTTGTGGGGCTTTTT | 10533 |
| rs538072245 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11478861 | CTCTTATTAACATGC[A/G]TTTATTATTTAATAA | 10533 |
| rs538087392 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508180 | AAGCATTTCACTCTT[A/G]CTAGCTATGGACAGG | 10533 |
| rs538092878 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11542732 | GGGCATCCTCCCGGG[-/C]CACCCCCTCCCGGGC | 10533 |
| rs538097400 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11352303 | TGTGAATAGTGCCGC[A/C]ATAAACATATGTGTG | 10533 |
| rs538115806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452356 | CGCCACTACACCCCA[G/T]TCTGGGCGACAGAGC | 10533 |
| rs538132718 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300479 | ATCTTCTACAGAAAT[A/G]GAGAAACCAGGAGGG | 10533 |
| rs538158905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343118 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT | 10533 |
| rs538160602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351717 | GCCTTATAAATAATA[A/G]GAGATAATATACACA | 10533 |
| rs538183290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477538 | GCCGCAAAAGATAAG[A/G]GCGTTTGTTAGACAC | 10533 |
| rs538184215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391612 | TGCTTCTTGGAAGCC[G/T]TTTTACAGCCTCAAT | 10533 |
| rs538186470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398581 | AGTACTTAATAAAAA[A/T]GTGGCTCATGCCTGT | 10533 |
| rs538196102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484073 | AGGATAGTTTGCAGC[C/G]TAAGAGGAAGGTGAT | 10533 |
| rs538196554 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469344 | ATCCCAGCTACTTGG[A/G]GGGCTGAGGCAGGAT | 10533 |
| rs538197246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11363978 | TAAGTTTATTGCCAC[C/T]CTCTGACAGGAAGTA | 10533 |
| rs538206689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324700 | TAGGGTAAGAAATAT[A/G]CTTATTCTTTGAAAT | 10533 |
| rs538213139 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11410340 | ATTGTATTTTTTTTT[A/T]AATTAAAATTTGATA | 10533 |
| rs538215224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327877 | GTCTGGGGAGGAGGC[C/T]GGGGATTCTGCATTT | 10533 |
| rs538215797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494235 | AAATGAAACTACATG[C/G]AGGAAAACAGGAATT | 10533 |
| rs538236871 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11460621 | GCAATTCACAGAATT[A/C]ATTCCATAAAAATGA | 10533 |
| rs538239881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11317395 | CTGCCAAAATAATAA[C/T]AGTTTGAACAGTGCT | 10533 |
| rs538244249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280043 | CCCCAATTTCATTTC[A/T]TTTCTTTTCTTTTTT | 10533 |
| rs538250958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454606 | TACCATTATCCCGGT[C/T]TTTCTGGGCATATGA | 10533 |
| rs538255310 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11335660 | TTATTCTTACATCCT[A/C]CTCTCTATGATAAGG | 10533 |
| rs538272652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366527 | TGCTATTTATGCTGT[C/T]GTATCTCATTTGAAT | 10533 |
| rs538285210 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456775 | TTTTTTCCTCTCTTT[C/G]TACTTTAACCCTAAA | 10533 |
| rs538289088 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273011 | AGAAATAGAGTCAAA[C/G]TTCTAATTTTATAAG | 10533 |
| rs538290849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507245 | TAAGATCACACCACT[C/G]CACTCCAGCCTGGGA | 10533 |
| rs538299804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379346 | CTTCAGTTATAGTTT[C/G]TGAAACCTGATTATA | 10533 |
| rs538321871 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11437796 | GAAAGCAAGTTTTAT[A/G]TACAGCGGCACCTCA | 10533 |
| rs538339371 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365842 | TCTTTCAAAGGTCTT[G/T]TGAGTTGAAAGATCC | 10533 |
| rs538345653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428189 | AAATGATTGCATGGG[A/T]GCAAAGATCTATAAA | 10533 |
| rs538354357 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11449652 | TTGGCATAAATCTAA[C/T]GTGTGTATTTGGATC | 10533 |
| rs538359737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420998 | CTGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC | 10533 |
| rs538363270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546115 | CACTCCAGCCTGGGT[A/G]ACAGAGTGAGGCCCT | 10533 |
| rs538375737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459891 | AGATGCTATTCTAAC[C/T]GTATTAACATATTAA | 10533 |
| rs538382217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467230 | TAGCATGGGGCAGTG[G/T]TTAGTAACAACTCTG | 10533 |
| rs538395213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484417 | AAACAAACAAACAAA[A/C]AAACCACAAAAACGA | 10533 |
| rs538409985 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373818 | CTCTTTAAATTTTAT[G/T]CAGTTCTTATAAGAT | 10533 |
| rs538411402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401711 | CTTCACACTGGACTC[C/T]GGTTCTGCCTCCTAC | 10533 |
| rs538417273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446450 | CTCCTTAATTTAGTC[C/T]GTAGGGGAAACTTGG | 10533 |
| rs538420008 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11304023 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 10533 |
| rs538440335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449513 | TGAGAGAGAGTATGA[C/T]TGGTTTTAGTTAGTA | 10533 |
| rs538441184 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434860 | CTAATATTAGGAAAC[-/AG]AACATGGGAATCCAG | 10533 |
| rs538446597 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11519782 | TATCCAGGATAATCT[C/G]GATCTCCTGACCTTG | 10533 |
| rs538446634 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339445 | GACAGTGGAGGTGAT[G/T]CTGGAAGTGTAGGCT | 10533 |
| rs538452180 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11449716 | TCCCAGTTAGATGCA[A/C]AGCTTCTGGAGGACA | 10533 |
| rs538452623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11315660 | CACCCCTACAGTTAT[C/T]GAATCAGCTCCTCTA | 10533 |
| rs538477953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440569 | GACCTCGTGATCCGC[C/T]CGCCTCGGCCTCCCA | 10533 |
| rs538491957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11355192 | CAGAATGGAGATTCC[A/G]GAGTTCACACGAGCT | 10533 |
| rs538506777 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399629 | GCCCAGGCTAGAGTG[C/T]AGTGACACAATCTCG | 10533 |
| rs538516084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362181 | GTCAAAAATATCTCT[A/G]ACAACCTCTTAATTT | 10533 |
| rs538525093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494767 | GTTGAGGAGGGGACT[C/T]ATGCACTCTGTAAAG | 10533 |
| rs538541368 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306562 | TTATTATGTGACCTT[A/C]GGCAAGTTGCTTAAA | 10533 |
| rs538549287 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11485859 | ATAGTTGTAGATATG[C/T]GACGTTATTTCTGAG | 10533 |
| rs538559232 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11371832 | TAAAAGACCCTTGGC[A/G]CCTTGTTCCCAGTGC | 10533 |
| rs538578758 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11490228 | TCCCTTTACAATTAT[G/T]TAATGGCCTTGTCTC | 10533 |
| rs538582397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11540512 | TGGGCATGGTGGTGC[A/G]CACCTGTGGTCCCAG | 10533 |
| rs538588662 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273431 | CTCACTGTTCCTCCT[G/T]CAGGCTCTTGGAATC | 10533 |
| rs538594146 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11307194 | ACTTGTGGGCTTTGG[C/T]ATATTTCTCCAGAGA | 10533 |
| rs538594418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319574 | GTAATTCAATTTTCT[C/T]TCACCGGCCTGAACC | 10533 |
| rs538606030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414208 | GTAGCTGGGATTCCA[A/G]GTGCACACCACCACA | 10533 |
| rs538606165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276613 | CTCGACATTGCCAGA[A/G]TACCTGACCACTTTT | 10533 |
| rs538609860 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400257 | TCCAATGTAAGTTTT[C/T]AATAATTTACCCACC | 10533 |
| rs538611195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475796 | TTGACCCATTGATAC[C/G]CTGTACCCTAAGTAG | 10533 |
| rs538624200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284713 | TGCACCACCACTCCA[C/T]AATAATTTTTTAAAA | 10533 |
| rs538631712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383008 | CCTTTAAAACTGAAT[G/T]CTTCAATGTGAATTC | 10533 |
| rs538631887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11390019 | TCTTCCACAAAGGAC[C/T]TTGAAGGGAGAGGGT | 10533 |
| rs538652953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11553579 | AGCCGCACTGAGGAT[A/G]AGCTCGGTGGGGACC | 10533 |
| rs538670244 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11402675 | AAATATAAAATCACA[A/G]AATAGAAGGAAAATC | 10533 |
| rs538670308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535087 | ATCTGTAAAGGCCCA[C/G]CGGATTCTTCCTAAG | 10533 |
| rs538676044 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11286634 | CTGGCTCGATCACCT[A/G]GGCTGGAGTGCAGTG | 10533 |
| rs538683942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374865 | GCTGAAATCGCTCCA[C/T]TACACTCCAGCCTGG | 10533 |
| rs538691453 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11425980 | ATATAGTATTCCATT[A/G]CATGACTATACCACA | 10533 |
| rs538699669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382195 | GACAGACTGGGGAAG[C/T]AGAATAAGTTTCTGC | 10533 |
| rs538701446 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374319 | AATGGCCAACCAATA[C/T]AGTTCAATTGGGAAA | 10533 |
| rs538725073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481500 | ATTTTACGTGCAGGT[A/G]CTGAGGTCATTATTT | 10533 |
| rs538740758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11348235 | CATGGTGGCTCATAC[C/G]TGCAATCCCAGTGTG | 10533 |
| rs538754914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327104 | GTATTGAAGCCTGGA[C/G]AAATGTACTAGTCTG | 10533 |
| rs538764602 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273269 | TCCCTTTTTCATTGA[C/G]TACTTAGATTTTTTT | 10533 |
| rs538766852 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11384448 | GGTTCTTCTGTTGAT[-/G]GGTTATGATTAAACT | 10533 |
| rs538775764 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11503562 | AGGAGGTCAAGACCA[G/T]CCTGACCAACATGAT | 10533 |
| rs538784561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516447 | AAACACTGACAACAC[C/T]GAATGGTAGTGAGAA | 10533 |
| rs538786871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482147 | TGCTCCGCTCTGTCC[C/T]GCTTCCTTCCAACTG | 10533 |
| rs538791315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389489 | ATGGTTCTCTTCTCT[A/G]GAATATCTAATGACT | 10533 |
| rs538809332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314289 | GTTGTTAAGGCAAAG[A/T]TTATGTGTCAAGATG | 10533 |
| rs538819820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271500 | TGCTGTGATTACAGG[C/T]GTGAGCCACCGCGCC | 10533 |
| rs538822485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499340 | AGTTTTCCAAAGATA[G/T]GAGATCATCAGAAGG | 10533 |
| rs538823884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322315 | AGTAAATGATTTAAG[A/G]ATCGCAAATAGCTCA | 10533 |
| rs538823898 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11548185 | TCTTTTTATTATTGC[A/G]TTGTAAATGGCCTTT | 10533 |
| rs538849150 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444598 | TTAAATGTAAAACCC[A/C]AAACTATTAAAACCC | 10533 |
| rs538850383 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11277879 | AGACACTCCCAGAGC[A/G]GCCCTTTATAGACCC | 10533 |
| rs538859274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315276 | GGTACCTTTTTTTTG[A/G]GTTAGTTTTTAGCCC | 10533 |
| rs538893535 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11398516 | TTAAGAACTATTTTA[A/C]CTGAATGATTAAAAA | 10533 |
| rs538898344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504964 | CAAATCCTCATTTAC[C/T]GAGCAAAATGGGAAA | 10533 |
| rs538901283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536962 | CGTATACTCCCCTCC[A/G]TGTCTCCTGGTACTC | 10533 |
| rs538917170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528683 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGCGC | 10533 |
| rs538946964 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340186 | ACAGGTACAGAAGGG[A/G]CATACTTAATTTAAG | 10533 |
| rs538951880 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11317083 | CTGGCCTTGTGATCC[A/G]CCCACCTCGGCCTCC | 10533 |
| rs538959288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11422566 | GATCACTAAAACTTT[C/T]TCTGTAGCTCTTTTA | 10533 |
| rs538970172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313486 | GTAGTTATGTAGTTC[C/T]TTCCAAAGACAAACA | 10533 |
| rs538973501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415999 | GGCTACAGCTTCACT[A/G]GGGATTAGGAATTTT | 10533 |
| rs538977257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468128 | TCAGCTATAGAAGAG[C/T]GTGACTTTCATCCCT | 10533 |
| rs538979196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341426 | TATTGTGTTTAAGGG[C/T]GAATCTCAGTGCACT | 10533 |
| rs538987012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11277339 | CTGCTTTTATGGCAT[A/G]GTCCATCTACTCTGC | 10533 |
| rs538988363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334867 | GAGGCTGAGGCAGAA[G/T]AATCGCTTGAACCTG | 10533 |
| rs538990933 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11502293 | GTTAGTTACATACGT[A/G]TACATGTGCCATGCT | 10533 |
| rs539007457 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411826 | TTTGCCCTGTGTTTT[C/G/T]TTCTAAAAGTTTTAT | 10533 |
| rs539032978 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11541338 | AAAAGATTGTCCTTT[C/T]TCGTCAAATTACTGT | 10533 |
| rs539044472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376748 | ATTTATATTTTATTT[C/T]TATTTTTTGAGACGG | 10533 |
| rs539046747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292890 | CTTGCTGCTGTGCCT[A/C]GTTTTGGTCTGTGTT | 10533 |
| rs539070293 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11429805 | ATACAAAATCTAGCC[C/T]GGTGTGGCAATGTGC | 10533 |
| rs539086243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379649 | AGTGGACCTGTTCAA[C/T]ATTTTGGAAGACATT | 10533 |
| rs539097242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436697 | GGATGGATAAAATGT[C/T]AGCTATTACGCTGGA | 10533 |
| rs539111864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515888 | GCTGTGGGGCTTGAA[A/G]CCAGCATGAGACACT | 10533 |
| rs539157981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437326 | GCCTTTTCTTATGCT[A/G]TGGATAGCCTGTAAA | 10533 |
| rs539159916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429166 | TTTTTGGCCTGCCCA[A/G]TTTGTTAAATTCTGA | 10533 |
| rs539165604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475131 | CTGGGCAAGGTAGAT[G/T]ATATTGTTATTGTTA | 10533 |
| rs539168875 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408614 | TTGGGGAGGCCTTAC[A/G]ATCCTGGTGGAAGGT | 10533 |
| rs539170914 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11437610 | TGAAAATTCCCAAAT[A/G]TACCAGAAAGTTGAA | 10533 |
| rs539191642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484380 | GCCCGGATGACAGGA[G/T]ACTCCGTCTCAAAAA | 10533 |
| rs539195757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392238 | TTCATCTCCCATTTT[G/T]GTTAATTCTCAGCTT | 10533 |
| rs539198337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492528 | CTTTGCTGAGGGACT[C/T]GTGACAGGGGTTCCC | 10533 |
| rs539211690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11538664 | CCTGGTCAGTGTGAT[A/G]AAACTCCGTCTCTAA | 10533 |
| rs539215643 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11412215 | AACTAGAGAGGGGTA[A/T]GGAAGCATCTGGTGC | 10533 |
| rs539226516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419605 | TTGCTTCTCATGAAT[A/T]GAAAATCATTATATG | 10533 |
| rs539226966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323147 | GTGGTGTGCTGGTAA[A/G]TGTTTAACAGCCAGC | 10533 |
| rs539230196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450292 | TAGTGTCTTTCTTAC[A/G]TATTAGTTGGGCCTG | 10533 |
| rs539239610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11456669 | CTTATTTCTTTCTAC[C/T]CCCCCCACTACCGAC | 10533 |
| rs539273048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364221 | GCTCAAGAAGTTAAG[A/G]TTAGAAAATTTTCCA | 10533 |
| rs539294964 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456219 | TGTTCTGAACATCTC[A/T]TATAAATGGAATCCT | 10533 |
| rs539302036 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376694 | TGGGCCCAGAGCAGA[G/T]GGACCTTGGAGTGCA | 10533 |
| rs539331788 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11387356 | TTTTTAAGACTACCT[A/G]ATTAGTAGTTAGAAC | 10533 |
| rs539333590 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11520099 | ACTTTTGCACATGAA[-/TTTG]TTTAATTTTCACCAA | 10533 |
| rs539334268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328729 | TGCCATTCAGCCATT[A/T]CTCACAATGGTTATA | 10533 |
| rs539334379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335543 | GTCTGGTCTGTGTGT[A/C]TGACAAGCTGCCAGG | 10533 |
| rs539334734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541710 | TCTCCAGTTTTCCTC[C/T]TCCTCTTCTCCCTCT | 10533 |
| rs539363052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11548130 | ATTACAGGCATGAGC[C/T]ACCACGCTTGGACTT | 10533 |
| rs539368308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543996 | CCAGGCTGGCCTCAC[C/T]ATCTGCTCTGGCCTT | 10533 |
| rs539369177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329133 | AAAGACAGTATTTAT[A/G]GCATGATCCCATGTT | 10533 |
| rs539382940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508754 | CCATGCACAGCCCTA[C/T]GTAGCCTATTTTGAA | 10533 |
| rs539389266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288351 | TATTATTTCATTTCA[A/G]CCTTTACTGAGCTCT | 10533 |
| rs539414076 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11361957 | TCCCTTAATAACTCA[-/T]TATCTCTTTTGGATG | 10533 |
| rs539428454 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11513102 | CTAGATACAGAGTGC[C/T]GATTGGTGTATTTAC | 10533 |
| rs539432514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11471784 | AGTCTCTATCGCCCA[A/G]GCTGGAGTGCAGTGG | 10533 |
| rs539449785 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11346028 | CTCTTACCAATTAAC[A/T]TGTCATTAAAAATGA | 10533 |
| rs539451831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520657 | CACATTCTACACTTC[C/T]GAGCTCGCCCTGTAC | 10533 |
| rs539452203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527641 | GAGTTACAATGTATG[C/T]CCCACAATCATATAG | 10533 |
| rs539467448 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11432456 | TTTATGAAGAAGGAG[C/G]CTTGCATAAGAATGA | 10533 |
| rs539467557 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385250 | GGCCAGGTTGGTCTC[A/G]ATCTCTTGACCTTGT | 10533 |
| rs539498897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447831 | CTGGGCCAGGGGCAG[A/G]TCATACTGATTGGCA | 10533 |
| rs539510951 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386860 | TCCCAAAAGGAGATG[A/G]AATATACAGCCAGAG | 10533 |
| rs539523184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525846 | GGTGTGAGCCACTGC[A/G]CCTCGCCAGTTATAG | 10533 |
| rs539525905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11534028 | CAGCACTTGTGAGCC[A/G]TGCCACTGTCAGAGT | 10533 |
| rs539527646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11412844 | TATTTATGATGGGGT[A/G]TATTTCCATTTATTT | 10533 |
| rs539528809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405514 | GGTTCTTACTCCACT[A/G]TTTTTGCTGACATTG | 10533 |
| rs539543563 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11318189 | TGCCTGTCTGCTTGT[C/T]GGATTCAGGCACACT | 10533 |
| rs539548285 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555137 | ACTGATAGCCATCCC[C/G]CAGGATCCTTTCCCC | 10533 |
| rs539553013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11440356 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 10533 |
| rs539565218 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11421754 | AATCACCCTGTATGG[A/C]AGCTATTGCCTTATT | 10533 |
| rs539574714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544467 | CAAGAAGTACCCACC[A/G]CTGTGTGTCCCTGTG | 10533 |
| rs539576793 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11274998 | AAAAGACAAGCAGGG[G/T]ACCAGTTGGGTATAG | 10533 |
| rs539578005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325487 | GACCAGCCTGACCAA[C/T]ATGGTGAAATTCTGT | 10533 |
| rs539582402 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459925 | TCCTTACAAGAGCCC[G/T]GTGTGTTAGGAACAG | 10533 |
| rs539595577 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11345495 | TGTTTCTGTGTTGAC[G/T]CACCTTTTTAGATTT | 10533 |
| rs539599196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339649 | CATGAGAAGGTAGCA[A/G]GTGTGTTCTGCAAAG | 10533 |
| rs539614094 | in-del | -/TG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490268 | TGTTGGTTTAAAGTC[-/TG]TTCTATCAGAGACTA | 10533 |
| rs539623925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290099 | ACAGGGTAGGGCTCC[C/T]CTCCAATTAGTGTTC | 10533 |
| rs539626272 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11508969 | TATGTGCAAGAGAGC[A/G]TAAGTAGAAGGAGAC | 10533 |
| rs539634206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458543 | GCCGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 10533 |
| rs539634245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465855 | AGGGATAAGAAGAAG[A/G]GGAGAGAATTGGAAA | 10533 |
| rs539640103 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557528 | CCCACTGCTCATCGC[A/G]AGGGCCTGCCAGGAG | 10533 |
| rs539645483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458895 | CTCCTGTCAGATCAG[C/T]GGAGCATTAGATTCT | 10533 |
| rs539649450 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326224 | TGTTTCAATGTTTTG[A/G]AAGTAGAAATGCTAG | 10533 |
| rs539655496 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11515136 | GAGCCACCGCGCCTG[A/G]CCTAGGTTTTAAAAT | 10533 |
| rs539659193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474382 | AGGTAGGTGGACCAC[C/T]TGAAGTCAGGAGTTC | 10533 |
| rs539673134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545463 | CCCATCCTCGGCTCC[C/T]GGCTGGAGAGTCTCC | 10533 |
| rs539676685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367606 | TTCTGTCTCTGGGTC[C/T]ACAGGCAGAATTTGG | 10533 |
| rs539680517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11380111 | GGGTCAGCATTTGAC[C/T]GCAGCCTCACCAGCT | 10533 |
| rs539681619 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11336666 | TATTATTTTAAATTA[A/T]TTTATTTTATTTTAT | 10533 |
| rs539684365 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11432495 | ACTTTTGGGACTTGA[C/G]GGAGAAGCTTGGGAG | 10533 |
| rs539692793 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394316 | TTAACTAGTGATAGG[A/G]CAGGTGATTTAAACC | 10533 |
| rs539703914 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11433361 | AATCAAACATATGAA[A/C]ACCTTAGCCATGTTC | 10533 |
| rs539710296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425411 | AAATCTATTTCTTGT[A/G]TAATTACTGTTCTGG | 10533 |
| rs539722931 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11418859 | AGGGGAAGCAAGGCA[C/T]TTCTTACATGGCGGC | 10533 |
| rs539725559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353537 | CAAATCTCATGTTGA[A/G]TTGTGATCCTCACTG | 10533 |
| rs539741284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331723 | CCCTCCCTTCTAGCT[A/G]TCTGGGTTTCTTTCA | 10533 |
| rs539748966 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11547500 | GTGTACAAGTTTTTA[C/T]GTGGACACGTTGTCA | 10533 |
| rs539763934 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11308653 | TCTGTAACCCTGATG[-/T]GCCTGGTATATAGTA | 10533 |
| rs539764119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551227 | CGGGGGTTTCATGGC[A/G]TCTCCCTCGGCCCAT | 10533 |
| rs539767356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11434448 | CCATCCTGGGACTGT[A/G]CCCTGCCTTGATTTT | 10533 |
| rs539775295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399799 | GGCTGGTCTTGAACT[C/T]CTGACCTCAGGTAAT | 10533 |
| rs539791208 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | ATG7 | GRCh38.p7 | 3:11306116 | CTTTGCTTACTCTGA[G/T]GACTGTGAGGCCTTT | 10533 |
| rs539792055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394486 | TTAGGGCAATTTTTT[A/G]TTTTATGGCCATTTG | 10533 |
| rs539806150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522624 | CCCCAAGGCAGCAGA[C/T]ATAATTATTCATAGA | 10533 |
| rs539806587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484907 | CATAGTATTCCATGG[C/T]GTATATGTGCCACAT | 10533 |
| rs539807562 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447208 | CAGTGGCTTACGCCT[A/G]TAATCCCAGCACTTT | 10533 |
| rs539807914 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353902 | CTAACACAGGAAATA[C/G]AAAGAAGTGTACCAG | 10533 |
| rs539818800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443385 | TGAGGTGGTTTCCTT[C/T]TCTTCGTTGTTGTTT | 10533 |
| rs539819817 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11299950 | TTTTTTTTGAGACAG[G/T]ATCTCACTCTGTCAC | 10533 |
| rs539830877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305595 | CCCTTTGTGATTTCT[C/T]TCTCTTCAAGACCAG | 10533 |
| rs539866067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353055 | GGTATTCCTTACTTG[A/T]TAAGTTATTGCAAGA | 10533 |
| rs539882493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436986 | TAATCTTAGATAGTG[A/T]TGATGGTTGCACAAC | 10533 |
| rs539886169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453040 | GGGTATTGGAAGCAG[A/G]CAGTCCTTCCTTTCT | 10533 |
| rs539893892 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11479335 | CCATATTTGTGTGAA[-/T]TTCAAGAAGTCAAAG | 10533 |
| rs539895200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11375311 | ACAAACTTACAATAC[A/G]GCAATTTAAAAAATG | 10533 |
| rs539896830 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11324418 | GAAAGATTAAATGAT[A/G]TTCAGCTTAGTGTTA | 10533 |
| rs539896940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516039 | TCCTTTTTAAAAAAA[A/C]AAAAAAACAAAAAAA | 10533 |
| rs539913126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368520 | GACAAGGCTAGGCAC[A/C]GTGGCTCACCCCTGT | 10533 |
| rs539914854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442902 | CTCCAGCCTGGGCCA[C/T]AAAGCAAGACCTTGG | 10533 |
| rs539925982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490926 | CCTTCATTTCAACTT[C/T]GGTGAATCTGACAAT | 10533 |
| rs539931724 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11465401 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 10533 |
| rs539933234 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11296027 | AGGTGATCCACCCGC[C/T]TTGGCCTCCCAAAGT | 10533 |
| rs539939338 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478858 | TTTCTCTTATTAACA[G/T]GCATTTATTATTTAA | 10533 |
| rs539946500 | snp | A/C/G/T | 8.27024e-05 | 0.00643009 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347886 | ACACAGGGTTGGGGC[A/C/G/T]TGAGACACATCACAT | 10533 |
| rs539946856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360468 | GCTTTTATAATCTAA[A/T]TACACTTACATGCAA | 10533 |
| rs539978879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473497 | GAACGGATGGAAAAA[A/C]TCGGGATTCAGTTCT | 10533 |
| rs539984479 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11511822 | ACTCAGTACACCCTC[C/T]GCAGCCACTGGCCCA | 10533 |
| rs539984746 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | ATG7 | GRCh38.p7 | 3:11391982 | GGTAATTTCACTTTA[A/C/G]ATTTTTAGCAGCTTC | 10533 |
| rs539990666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11461753 | GACTCTGGGCCGGGC[A/G]CAGTGGCTCACACCT | 10533 |
| rs539999540 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11419716 | AATGCCTAGGCAGAG[A/C]AGATAGGTTTGATAT | 10533 |
| rs540022137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388199 | CTTTTCCTCAACTGT[A/G]GTAAAGGGAGATGCA | 10533 |
| rs540032796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277510 | CAGCTGGGCCTCTGG[C/G]GGTGACATCACATAT | 10533 |
| rs540050200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547527 | GTCATTTCTCTTGGG[C/T]AGTTACCTAGGACTG | 10533 |
| rs540052950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289516 | ACATCAACTATATCC[C/T]CTTATGAAATAGGCC | 10533 |
| rs540057321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370921 | TTCAGCTTTATTCCT[C/G]AGGCTTTAGAGCCAG | 10533 |
| rs540058882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11381658 | TTAGCAAAATTATTT[C/T]CTCTTGGTGATCATT | 10533 |
| rs540059937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427539 | AAATAAATTATCGGC[C/T]GGGCGAGGTGGCTCA | 10533 |
| rs540080987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335675 | ACTCTCTATGATAAG[A/G]CTCATGCTTGATGAT | 10533 |
| rs540085442 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441297 | TGCCCAGGCTGGAGC[A/G]CAGTGACATGATCTC | 10533 |
| rs540099821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328857 | TTTGGGAGGATGAGG[C/T]CAGTGGATTGCTTGA | 10533 |
| rs540102708 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11423480 | TTTCAATTTTTTTTT[C/T]TTTTGTAATCACTAA | 10533 |
| rs540105563 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11341152 | CTGCAACCTCTGCCT[A/C]CTGGGTTCAAGTGAT | 10533 |
| rs540114178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485310 | TGTTGAGCATTTTTT[C/G]ATGTGTTTTTTGGCT | 10533 |
| rs540151118 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11443787 | AGATCAAGAAAATTT[-/C]CCCCCCTGCTTTTTT | 10533 |
| rs540160917 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417789 | GCATTTAAAAAATTA[C/T]TATTATTATTATTTT | 10533 |
| rs540163015 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350165 | TGCTTTAGAAGCATT[A/G]TTAATGTTTTTGTCC | 10533 |
| rs540163733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335060 | TTTCAGCGATTCTAT[A/G]CTCTAACACAGATGT | 10533 |
| rs540174838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297862 | CCAGGACCACACAAG[A/G]TGGCAAAAATTTCTG | 10533 |
| rs540182559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387402 | CTTTCCCTGTCACCT[A/G]TGGTCACAAACACAT | 10533 |
| rs540187074 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11383265 | TACTTCATCTTTCTT[C/T]ATCTTTCTTAACTTC | 10533 |
| rs540204851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389181 | GAGGTTGCAGTGAGT[C/T]GAGATGGTGCCACTG | 10533 |
| rs540231972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11300753 | CCCATACAGCCATTC[A/G]GTTTTTCACTTTCAG | 10533 |
| rs540243892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389713 | TCTTGAGTAAAGGCA[A/G]CATCATTGGAATATA | 10533 |
| rs540264050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11365031 | GGAATCAGTCATACA[A/G]TGGTTTAAATCCCAG | 10533 |
| rs540280587 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496511 | GCTCTTCTCTGAGGG[C/T]TGCTGAGGCTGGGAC | 10533 |
| rs540280719 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11290335 | CCTGGGTCCCCCACA[G/T]CCCAGCGCGGTGATG | 10533 |
| rs540287708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371368 | CAGCGAGTAAAGGGG[C/T]ACAGCGGAGAAGGCA | 10533 |
| rs540291208 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315959 | GTTGGTCTTGAATGC[A/G]TGACCTGCTTCGGCC | 10533 |
| rs540301554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521922 | CGCCGCTGCCGACAA[C/T]AATAACAAAGTAGAT | 10533 |
| rs540302626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356803 | TGCACAATACTTAAT[C/G]GATTAATTAATGAGA | 10533 |
| rs540319627 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11485915 | TATCTCTGTTTTGGT[A/C]CCAGTACCATGCTGT | 10533 |
| rs540321790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492197 | CCATCGGAAAGGCGC[A/G]GTATTAGGGTGGGAG | 10533 |
| rs540324101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481200 | GTTTAACCGGTACAA[A/G]GTTTCAGCTGGGGGC | 10533 |
| rs540335957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486354 | GTCTGTTATTGCTGT[A/G]TAAGAATGCTTGTGA | 10533 |
| rs540343545 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11404012 | ATTTAAAAGAAATCT[-/C]CCCCCCCAGATTTTT | 10533 |
| rs540344818 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352097 | ATGAGTGAGAACACG[C/T]GGTGTTTGGTTTTCT | 10533 |
| rs540363190 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11401915 | AGAAATGCATGTTTT[A/T]ATTGGATTGGAAGCC | 10533 |
| rs540363595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11395736 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10533 |
| rs540384794 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11492719 | GCAGGAACTAGCCGG[G/T]CACTTTAGCACTGGC | 10533 |
| rs540387044 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415472 | CTCTTTTGTAACAAC[A/G]CCTAGCTTAAAACAC | 10533 |
| rs540398939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391200 | GAACAAAAAAGGGCC[G/T]GGCCTCAAGATGTGA | 10533 |
| rs540409610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383683 | TCTAACTGCTGACCT[C/T]GTGATCCGCCCGCCT | 10533 |
| rs540425169 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285620 | CCAGGAGCCTTCCTC[A/G/T]TGGCCTTCTCAAGTC | 10533 |
| rs540435604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391852 | CTCAGAGAAATTACA[C/T]GAAAGTCCAGGATTT | 10533 |
| rs540437138 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330891 | AATCAAGAGTAACTG[G/T]CTGTTTAACTTGATC | 10533 |
| rs540439418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477302 | TAAAATAAAATGTAA[A/G]TAAGAATTTTTGTGC | 10533 |
| rs540443003 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11284962 | CGCCATTCTCCTGCC[G/T]CAGCCTCCCAAGTAG | 10533 |
| rs540462179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415509 | TACAGCCATACAAAA[A/T]CATTTTTTCTTTATA | 10533 |
| rs540506014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516831 | CTCACACCTGTAATC[A/G]CAACACTTTGGGAGG | 10533 |
| rs540513632 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11488566 | GCCAACCACCACCCG[C/T]GGCCACCATGGCCGG | 10533 |
| rs540518820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11430839 | TCAAGAAAAGCTTCA[C/G]AGGAAGAGAACAAAT | 10533 |
| rs540521337 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293222 | TTGGCATACAGACAG[A/G]ACTTGTTGTAGAAAG | 10533 |
| rs540524622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546909 | GCAGCACAGGCTGAT[A/G]CCATCCTCTCCCTAA | 10533 |
| rs540524744 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464158 | AGGCGGATCACTTGA[C/G]CCCAGGAGTTTGAGA | 10533 |
| rs540526117 | snp | A/C | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11483172 | CCTCACATTTTAATA[A/C]GCATTCTCCCCGTCC | 10533 |
| rs540559257 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11476081 | AAGGACTAGGGTGTT[C/T]ATGTGTGCACAGAAA | 10533 |
| rs540565832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396745 | CGAGATGGCGCCACC[A/G]CACTCCAGCCTGGGC | 10533 |
| rs540567853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308684 | GACAATAAGTAAATA[A/T]TTGCTGAAGGAGATT | 10533 |
| rs540578896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292286 | GGAGACAGAGTCTCG[C/T]TCTGTTGCCCAGGCT | 10533 |
| rs540587071 | in-del | -/AGAGTGTC | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11389378 | TAATCATAGTTTTCT[-/AGAGTGTC]TGACCTTCTCTAGTT | 10533 |
| rs540588795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530305 | GTGTGTGCGGTGCGC[A/G]TGCAGTCCCTGTGCT | 10533 |
| rs540588915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537075 | TCCATCCCTCTGCAC[A/G]GGGCCTCACCCACCC | 10533 |
| rs540593013 | snp | C/T | 3.33472e-05 | 0.0040832 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315481 | TGATTTCTTCCAAGG[C/T]CAAAGGACGAAGGTC | 10533 |
| rs540603766 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11367881 | AAAAATCATTTTGTT[G/T]ATGTGTGGAATAGAG | 10533 |
| rs540607336 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366430 | ATGTGTTAATCTTTT[C/G]TACAGAGACATTTCA | 10533 |
| rs540611195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456807 | TGTGTCACATTTTTT[C/T]GCGTTCACACTGTAT | 10533 |
| rs540627706 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271670 | GATTCTGTTCTTTCA[C/T]ATATAACTTGGGGAT | 10533 |
| rs540633743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450924 | TCCAGGGTGTATTAG[C/T]TGTTACTAATTTCAT | 10533 |
| rs540653966 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11490539 | CTGGTTATTTTGCTC[A/G]TTAGTTGATGCAGTT | 10533 |
| rs540662352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358245 | AGGTCAAGGTGTTCT[A/G]GGATGCAGAGGTGAA | 10533 |
| rs540681584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11453262 | TGAAAGTGTGGAAAG[G/T]CCTGTCCCCAAGCTT | 10533 |
| rs540684374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366949 | AAAGACTGAAGAATA[A/G]CGCAGCCATATATGG | 10533 |
| rs540699492 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11365606 | ACCAGTCCTATCTGG[A/T]GATTTGCAAGGACAG | 10533 |
| rs540699831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495833 | AGTTTTATTTAACTT[C/G]CCACATTCTCCCTTT | 10533 |
| rs540703976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526325 | GAGCCCAGGGAGGCC[A/G]AGGCTTTAGTGAGCC | 10533 |
| rs540705523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329393 | AAAAATTTATCAGCC[A/G]TGTTTTCATTTAACC | 10533 |
| rs540722145 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11416176 | TGTAGTTTTCTAGTA[A/G]TGTCTTTATCTGGCT | 10533 |
| rs540735159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499543 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCT | 10533 |
| rs540736621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408772 | GACCCACCCCCATGA[C/T]TCAGTAGTCTCCCAC | 10533 |
| rs540739033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542325 | CAAATATAGCGGGAC[C/T]CTGAGGTCCATTTTC | 10533 |
| rs540741218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322676 | AAGGTTTTGACATTT[A/G]TATTTCTCATAATTT | 10533 |
| rs540755823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331945 | AAGTGTTGTCGAAGA[C/T]GTGGAGCAAATACTG | 10533 |
| rs540761754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278059 | CCTGTAGGCAGTCAG[A/C]CCTTATGGTTGTCTT | 10533 |
| rs540786393 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11524805 | AAACAAAAACAAAAA[A/C]AAAAAAAAACAAAAC | 10533 |
| rs540792513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302728 | AGGAATGACATACAG[C/T]TGAATAGCTAACAAT | 10533 |
| rs540792643 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11309475 | TTTTGTTTTTTTAAA[A/G]ACAGAAACATGTTTT | 10533 |
| rs540814398 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11493650 | GAGAGATCAGGACAG[A/G]TAAGAGTCTAAGCCT | 10533 |
| rs540823185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518083 | TGAGTGGGAGAGAGG[A/G]AGGGGACCAAGGTGC | 10533 |
| rs540823905 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306782 | CCTGTTTTTTAGTTC[C/T]TGAGTTATGATATTC | 10533 |
| rs540832908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11294551 | TCCATTGGGCAAAAT[C/T]ATAAAAATTCTTTCA | 10533 |
| rs540836069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297995 | AAATCACTGTGTCAT[C/T]GGTGAAACCCTGTCT | 10533 |
| rs540838301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394655 | ATCAAGAGATACACC[C/T]AGGAGTAAGGGTGAA | 10533 |
| rs540860453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353193 | TGATGCCTATAATCC[C/T]AGCACTTTGGGAGGC | 10533 |
| rs540874922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514091 | ACTGTGTTTAGTTTA[A/G]CACATGACTGTCTCA | 10533 |
| rs540877551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11439229 | GCCCACCACCACGCC[C/T]GGCTATTTTTTGTAG | 10533 |
| rs540903994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444697 | CCAAAAACAATTGCA[A/T]CAAAAGCAAAAATTG | 10533 |
| rs540906295 | snp | A/C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11361386 | GCCTCCTGGGTTCAA[A/C/G]TGATTCTCCTGCCTC | 10533 |
| rs540918090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11491030 | GCCTACCTTGCTAGA[C/T]TGGGGAATTTCTCCT | 10533 |
| rs540924198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399434 | TGATATTATTAAGGA[G/T]GCAGGCAGATTTAGG | 10533 |
| rs540927603 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11531533 | TCACATGGTCCGCAA[A/G]TCTGCATATTGGTTT | 10533 |
| rs540932401 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11484995 | TGTGAATAGTGCCGC[A/G]ATAAACATACGTGTG | 10533 |
| rs540955583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397513 | CCCAGGCTGGAGTGC[A/G]GTGGTACGATCTTGG | 10533 |
| rs540960306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484704 | ATCCCTCCCCTGACC[C/T]CACGACAGTCCCCAG | 10533 |
| rs540963628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309150 | GTCTGCTCTTCTCTC[C/T]GAAGCTACTACCTTC | 10533 |
| rs540966901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399929 | TTCTTGACTGGGTTG[C/T]AGTTACACAGATGGT | 10533 |
| rs540984004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318411 | TTCAGAGAATTGATA[C/T]GGGTGATACTTTGGT | 10533 |
| rs540986643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405666 | GATCTCTCACTCTGT[C/T]GTCCAGGCTGGAGTG | 10533 |
| rs540989125 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341712 | TTTGGCCTCCCAAAG[C/T]GCTAGGATTACAGGC | 10533 |
| rs540999866 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11530057 | AGAGGTGTCGTTGGC[C/T]TTTTTGAGGACGCCT | 10533 |
| rs541020925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539679 | TTATATTGTGAAACT[C/T]CCCCCGTCTTAAGCT | 10533 |
| rs541022917 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400951 | TAAATAGTGATATCA[C/T]GCAAAGCAATTTCTT | 10533 |
| rs541028670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446794 | AGCTATGCTCCAGGG[A/G]GAGGTGGTTGAAATC | 10533 |
| rs541036739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510540 | CTCAACCCCCCATCT[C/G]CAAAGCTGTCCCCTC | 10533 |
| rs541048192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283484 | TGAGTAAATCCAGGT[A/G]CAGGGGGGTGAAGGA | 10533 |
| rs541090836 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452908 | GTTCACTAAGCACCT[A/G]TTGTGTGCCAGTTCC | 10533 |
| rs541108818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325325 | TTGCTTTTGTTGTTA[C/T]TATTTGTTAAGCGCT | 10533 |
| rs541114088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509271 | TGGCTGCTGCCGGCA[A/G]GAGGGAGCCGAGCTG | 10533 |
| rs541117679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434809 | AGCGAGAAAGAAGGG[A/G]GGAAATCATAAATGC | 10533 |
| rs541118972 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475030 | CAGGAGTGACTTAAC[-/T]TTTTTTTTTTTTTTA | 10533 |
| rs541137041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426191 | TGTTCCACATCCTTG[C/T]CAGCACTTGGTATTT | 10533 |
| rs541144629 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11420288 | CATATTTTTAAGCCA[G/T]TGCTATTAATAATGT | 10533 |
| rs541146276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11480426 | CCTATAGTCCCAGGT[A/G]TTTGGGAGGCTGAGG | 10533 |
| rs541149928 | in-del | -/TC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515694 | GAACTGTTCTCTCTT[-/TC]TCTCTCTCTCATACA | 10533 |
| rs541162230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273970 | ATGTTGCTAAACTGC[A/T]TTCCCATCCCCCAAC | 10533 |
| rs541172845 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456159 | ACCACCCTCTGGCCC[C/G/T]CTAACCCTGAGCGAT | 10533 |
| rs541177509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11388370 | CTCCCTCTGCTAGCA[A/G]GGTGCATTGACTTGA | 10533 |
| rs541179354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427855 | TTTTTCCAAATGCTC[A/G]CTGTTCTTAGAAAAG | 10533 |
| rs541181725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535398 | TCCCTGTGGAGGAAC[C/T]CTGGCTTTTGTGATT | 10533 |
| rs541182222 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412263 | CAGTTATTTGATTCT[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs541186138 | in-del | -/TCT | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11508481 | AAATAAGAGACAGAG[-/TCT]TCTTGCTCTGTGGCC | 10533 |
| rs541186991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480025 | TCCCGTCTCTGGGGT[A/T]CACGACATTCTCCTG | 10533 |
| rs541211040 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556585 | TCCTGCACTTTTACA[C/G]ACAAATCTACGACAA | 10533 |
| rs541214597 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11468734 | GCTTGGGATGGGGAT[-/G]CTTCCTGAATGCCCA | 10533 |
| rs541221688 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409376 | CACGATCGTGAGGGT[A/G]AACAACTATTGACTA | 10533 |
| rs541225413 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11448477 | CTCTGCTTCAGGACA[G/T]GTGCCTTTAGTCTCC | 10533 |
| rs541230697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387746 | GAGGCTGAGGCAGGC[A/G]GATCACGAGGTCAGG | 10533 |
| rs541253971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454708 | TTGTTCAGGGGCAGC[A/G]TTTCAATCTACCTAA | 10533 |
| rs541261126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535826 | TGGACCTGCCAGCTT[C/T]GCACCCTTGCTTGAA | 10533 |
| rs541271800 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11431164 | CCAGCACTTTTGGGA[A/G]GCCGAGGTGGGTGGA | 10533 |
| rs541276861 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11448983 | AGGGTAAAAATGTCA[C/T]ACAAAGTCTGTATTG | 10533 |
| rs541295838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447491 | AAAAAAAAAAGTAAT[A/T]TATTGCTTAATGAAA | 10533 |
| rs541296910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362286 | AAAAAATACTTGTAG[C/T]AAACCCTAGAATCAC | 10533 |
| rs541306159 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336058 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTCTCGCTC | 10533 |
| rs541310969 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554819 | CATGCAGATCTGGGA[C/T]ATGAGCGATGATGAG | 10533 |
| rs541319142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11413724 | TTGTCTAGCTTTGGT[A/G]TCAGGCTACTGCTGG | 10533 |
| rs541331313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414512 | ACAGTTTTATTTCTT[C/T]CTTCCCAATCAGAAT | 10533 |
| rs541341153 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11377402 | CATTCAACCAATACC[A/G]TGCACGGCATCTTCT | 10533 |
| rs541345499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327413 | ATGATAGTGTACATA[A/G]GAATCACATGCGGTA | 10533 |
| rs541347455 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390997 | TAGTTGCAGTACCAT[A/C]GCCATGAAGTTGGAA | 10533 |
| rs541349320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319771 | CTTCCCCCTACCACC[C/T]CTGTGTCTTGTGGAT | 10533 |
| rs541360004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11534241 | AAAAGCTCCCAGAGT[C/T]TTAGCACTGTGCCCT | 10533 |
| rs541389601 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11466918 | GCAGATCACCTGAGG[G/T]CAGGAGTTTGAGATC | 10533 |
| rs541394251 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11511741 | CCTGAGCCCTGCCCC[A/G]AGGGAAGGCAGCTAA | 10533 |
| rs541396478 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11444178 | GCTATGTAGTGTTTC[A/G]TAATTGGATATATTG | 10533 |
| rs541401531 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11276178 | CTACCTTGACTTTTG[C/G]TCCACTAAGTTGCAG | 10533 |
| rs541404692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11294381 | GCACTCCACTACACC[C/T]GGCTAATTTTTTTTT | 10533 |
| rs541408883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457821 | CTGTGCAGTGGTAGC[A/G]CTTGTGTTGAATATT | 10533 |
| rs541425658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503225 | TGGACTTCAGACAGC[G/T]TCTGAGTACCTTCTC | 10533 |
| rs541442496 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11278367 | GAAATTATAAAAGTA[G/T]TATTTGGGAACTGAT | 10533 |
| rs541443985 | in-del | -/TGGAGA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11432200 | ATGACTGGTTGGCGT[-/TGGAGA]TGGGATGGAGATGGA | 10533 |
| rs541445968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11540085 | TAGAATTGCTGGGTC[C/T]TATGGTGGAAGTGTA | 10533 |
| rs541449066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11460053 | ATCCCAACTCTGGGT[A/G]ATCTCAGGAAAGAAC | 10533 |
| rs541474908 | in-del | -/TCT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11509099 | TTTAAGTACCTTAAC[-/TCT]TCTTATTTTATTAAA | 10533 |
| rs541479244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286038 | TTTGTAGAATGTTTT[C/T]CAACTTGGGTTTATC | 10533 |
| rs541497313 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529927 | AGCATGACCCATCTG[C/T]ACCACCATCCTCTTG | 10533 |
| rs541506223 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509135 | CCCAGGTCATGGGTT[-/G]GTTTTTTTTCTTTCC | 10533 |
| rs541506267 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557138 | CCCAGGGGGAGGGGA[C/T]AGAAACGCTCATTGA | 10533 |
| rs541506360 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11339171 | CATGCTGGCGGGCGC[A/G]TGTACTCCCAGCTAC | 10533 |
| rs541508253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551508 | GGACTGTCGCAGCTG[A/T]TTTAGAGGCTTCATA | 10533 |
| rs541508464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11511599 | TACTGTGCGCTCACA[C/T]TCCTCAGCCCTTGGG | 10533 |
| rs541514245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473032 | ATGATTTCTGACATT[C/G]AGTGACTGCTTGCTT | 10533 |
| rs541523670 | snp | A/G | 3.32116e-05 | 0.00407488 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333083 | GCTTCCAGAAATGGC[A/G]TTTAGCCCAGGTAAT | 10533 |
| rs541537896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423048 | ATAGGCATGAGCCAC[C/T]GGGCTTGGCCTATTT | 10533 |
| rs541543022 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483506 | GAGGAGTAACCACTG[C/T]ACTCCCCTTCCGATG | 10533 |
| rs541545102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551988 | TCCTGACCTCAAGTG[A/G]TCCACCCGCCTTGGC | 10533 |
| rs541552078 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556236 | CACTGCAGGCAGCGC[A/G]GCTCTGGGAAGAACT | 10533 |
| rs541563706 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11381198 | TCTGTAGTTTCCTTT[A/C]AGATATATCTGCTCA | 10533 |
| rs541568393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11293544 | TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGTGA | 10533 |
| rs541574867 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298052 | GGCGTGGTGGCATGC[A/G]CCTGTAGTCCCAGCT | 10533 |
| rs541582134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11316133 | GTTCAGGCCCCTCAT[A/G]TCACACTCCTGGACA | 10533 |
| rs541586152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324023 | CTTTTTCAGCAAATT[G/T]CTTGGCAGACTGATC | 10533 |
| rs541587288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383764 | TATCCTGGATATATT[C/T]ACTCACTTGCTGAAG | 10533 |
| rs541595023 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397050 | TACAAGATACAAAGC[A/C]CAAGAAGTCATGGTA | 10533 |
| rs541603801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554459 | GTGGACCACAAGGAG[A/C]ACAAGCTGGCTTGGG | 10533 |
| rs541609115 | in-del | -/T | 0.285594 | 0.247453 | intron-variant | ATG7 | GRCh38.p7 | 3:11551754 | GGTTCTTTTCTTTTC[-/T]TTTTTTTTTCTCGAG | 10533 |
| rs541613028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451097 | GAAATGAAAAAGACA[C/T]TGGATGCATACATTT | 10533 |
| rs541627066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451708 | ACACAGATTTTATAC[A/G]AATTTGTAATGCTAA | 10533 |
| rs541638769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11365196 | AAGGGCTCAGCAACA[A/G]TGTATATCATAGGCC | 10533 |
| rs541640498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370201 | TCCTAAAAAGGAATT[G/T]ATAAAGACTCTCATA | 10533 |
| rs541660447 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397214 | TGAAAATAAGATATA[A/G]GAACATAATATTTTA | 10533 |
| rs541668908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11279541 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCGGGT | 10533 |
| rs541672352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492006 | AAGTTTGAGCTTCCC[A/G]GCTGCTTTGTTTACC | 10533 |
| rs541691477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542521 | AAGACACCGGCAGAT[G/T]TACCTTGCCATGGGC | 10533 |
| rs541703152 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11366201 | TGTGGCCTGGGCGAC[A/C]GAGTGAGACTCCATC | 10533 |
| rs541704685 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11369558 | ATCTAAGGTGATGGA[C/T]GTATCCCAAGCCATT | 10533 |
| rs541705697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11463405 | GGTCTGCTAAACCTT[C/T]AGTCTTGTTGAACCA | 10533 |
| rs541709471 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506305 | AGCACATTTGATTAT[C/T]TAAATGTAATTCGAG | 10533 |
| rs541709934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11416917 | CATTTCTATTTAGTT[C/T]AAATATTTTAAATTT | 10533 |
| rs541714528 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11407102 | TAAATCAAAAGCAAG[A/T]TAGTTACTTCCTAGA | 10533 |
| rs541724311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417537 | ATTTTTTTCCATCTA[C/T]GTTTAATGAATAAAT | 10533 |
| rs541730316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543016 | GTGTGCACAGGCCTG[A/G]TCTGCTGCCCCCCTC | 10533 |
| rs541744933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323571 | CTCATAACATTGTCC[C/T]ATTACCAATCTTTTG | 10533 |
| rs541761991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491719 | GCTGCAGGTCTGTTG[A/G]AGTTTGCTAGAGGTC | 10533 |
| rs541774003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384371 | GCCCAGAAACCTGAT[C/G]TTGAGATTTCAGTGA | 10533 |
| rs541781081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330285 | TCTGAAGAGGCCAGT[A/G]TTTGCTTATATAGTT | 10533 |
| rs541792259 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11286532 | TCTATAGAAAGTTCC[G/T]TGTTTTTGTTTTGTG | 10533 |
| rs541795290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11457091 | GGACACAGTAGAAGC[C/T]GTTAAAAGGAAATTA | 10533 |
| rs541802918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378409 | AAATTCGGGCTGGGC[A/G]CGGTGGCTCACGCCC | 10533 |
| rs541811293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377726 | ATGAAGTTCTTTTCT[A/G]AGTAAACTTAATATA | 10533 |
| rs541820066 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11338431 | AATCTAAGAGTAGTA[A/G]TAAAATCAAACAAAA | 10533 |
| rs541828237 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11310638 | GTAATTCTGTAGTTT[G/T]TTTTTTTTTTTTGAG | 10533 |
| rs541834100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439332 | TCTCAGCCTCAGAAA[G/T]TGCTGGGATTACAGG | 10533 |
| rs541848022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378325 | CCCTGCCAAATTTTT[A/T]AAATGTCTTTATCAA | 10533 |
| rs541850311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358883 | AAAACGTAAGCTCCA[A/G]GAGGACAGAGACTTG | 10533 |
| rs541916504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11316866 | GCCATGTGAATATAT[C/T]AGAGCTGAAAAAAGG | 10533 |
| rs541919400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11341893 | GTCATGCTCTTCCCT[C/T]TTCACCTTGGCTGCT | 10533 |
| rs541921242 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11403294 | TCATTGGAGTAAGTT[-/AAAG]AGAGAATGGAGAATA | 10533 |
| rs541925396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11430676 | TAACTGAATACAGAA[A/G]TTAATGAGACACTGA | 10533 |
| rs541933437 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11391082 | ATCTTTTGTCTGAAC[A/G]GAGATCAGGTGCCGT | 10533 |
| rs541956522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342556 | AGATGTTATTGTAGA[C/T]ATATCTAAATATAGA | 10533 |
| rs541960787 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11432502 | GGACTTGAGGGAGAA[G/T]CTTGGGAGGGGGGGT | 10533 |
| rs541961086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483600 | GAGGTACACAGAAAG[A/C]CCCCATTTTGGCTTC | 10533 |
| rs541970355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410713 | CTCTCAAAGTTACTC[C/T]ATGGTGTAGCATGTG | 10533 |
| rs541972316 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317396 | TGCCAAAATAATAAC[A/C]GTTTGAACAGTGCTT | 10533 |
| rs541977523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524946 | AACACAGAAACAAAC[C/T]TCGTATATTCTATAT | 10533 |
| rs541979737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472046 | CTAGCCTTTTTCAGA[A/T]AATTTCTTCAAGATT | 10533 |
| rs541993314 | snp | A/C | 0.000281215 | 0.0118545 | intron-variant, splice-acceptor-variant | ATG7 | GRCh38.p7 | 3:11477132 | ATGTTTGTACCTGCC[A/C]GCATCTTTGAGATCT | 10533 |
| rs542005084 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11457698 | TCAATTTCAATTTGT[A/G]TGCCCCTCGCTTATG | 10533 |
| rs542010975 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284797 | TCAAGTGATCATCCT[A/G]CTTTGGCCTCCCAAA | 10533 |
| rs542015555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272754 | GAACACGGGAGATGG[A/G]ACATTTGGATTCCCA | 10533 |
| rs542022247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386760 | TGTATGATGGATTCC[A/G]TATGTATGATTGTGT | 10533 |
| rs542027862 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371598 | GCCTTCCATCAGAAT[C/T]ACCTAAGGAGCCATT | 10533 |
| rs542030550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507631 | CTAAAGTTATGGGTG[G/T]TTTTTGTTTTTGTTT | 10533 |
| rs542039321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373034 | TTTGTTTTGTCATGT[A/G]TTTATCGTTTTTATT | 10533 |
| rs542050857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11543770 | AGCTAGGCGTGGTGG[C/T]GCACGCCTGTTATCC | 10533 |
| rs542055489 | in-del | -/GTAAT | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11310281 | GGGCATATAAACACA[-/GTAAT]GTAATGTTGCTGTGT | 10533 |
| rs542056070 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11408373 | CTAGGAAGTTCCAAA[C/G]TTTCCCACATTTTGC | 10533 |
| rs542060960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380238 | ACAGTGGTTTAAAAC[A/C]AGCCTGAGAAAATGT | 10533 |
| rs542067254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11501104 | TACTAAAAATAAAAA[A/G]TTGGCCAGGTATGGT | 10533 |
| rs542071324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458341 | CCATCTCCGCTCACT[A/G]CAAGCTCCGCCTCCT | 10533 |
| rs542074364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549021 | TCACAAACAGAACAT[A/G]TTGTGAAGCAGTGAG | 10533 |
| rs542086110 | in-del | -/TT | 0.0363597 | 0.129838 | intron-variant | ATG7 | GRCh38.p7 | 3:11551754 | GTTCTTTTCTTTTCT[-/TT]TTTTTTTTTCTCGAG | 10533 |
| rs542088010 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555354 | CCTGGTGGAGCGGGA[A/G]GAGGAGGAGAGCCGA | 10533 |
| rs542088937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11359271 | TAATTTTTTGAGCTG[C/T]GGGTTGTGAGTGATT | 10533 |
| rs542094809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329970 | TTTCTTTGATTTTTT[G/T]TGATGACCTTGACAT | 10533 |
| rs542101130 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11506553 | TGAAACCCCATCTCT[A/C]CAAAAAAAAAAAAAA | 10533 |
| rs542108366 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11275343 | TGTCTTCCTCTCCTC[-/T]TTTTTTTTTTTTTCT | 10533 |
| rs542110337 | in-del | -/A | 0.0112537 | 0.0741632 | intron-variant | ATG7 | GRCh38.p7 | 3:11392475 | AAAAAAACAAACAAA[-/A]AAAACAAAACAAAAC | 10533 |
| rs542121811 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11347682 | CCAGGCACTGAGTAT[A/C]TAATTATGTTGTTTT | 10533 |
| rs542141845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464244 | AGGCATGGTGTTATG[C/T]ACCTGAAGTCCCAGC | 10533 |
| rs542151066 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337488 | CTCTCTCTCTCTCTC[-/TA]TATATATATATATAT | 10533 |
| rs542151888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278723 | AGTCAGGTGCTAGAA[A/G]AACAATGATGAATGG | 10533 |
| rs542157077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471183 | TCCAAAGGCTGGCTA[A/G]CCTTTGCTTCAGAAT | 10533 |
| rs542160933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493330 | CATCCAGCTGCTTCT[C/G]CTCTCTGCCAGCTGA | 10533 |
| rs542164207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525578 | TTTTTTTTTTTAAAC[A/G]GAGTCTTGCTCTGTC | 10533 |
| rs542165758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549782 | GGATCACATGGTGAG[C/T]GCACACTTAAACAGT | 10533 |
| rs542169684 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11365885 | TGGGAGATTTTGCTT[-/C]CCTGTTGGTACCCCA | 10533 |
| rs542171993 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412384 | GTTTATCCAAAAACA[A/C]CTATCTGTGGGACTC | 10533 |
| rs542176160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432603 | TCACCACTAAAGAAC[G/T]TATCTACATAACCAA | 10533 |
| rs542186018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480538 | ACATGACTGCCCTCC[A/G]GCCTGGGCAACAAAG | 10533 |
| rs542196092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448885 | CCTGGGGGTCTCTCT[C/T]CCCTGCCTGACATTT | 10533 |
| rs542205914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518220 | AACCATGCTGTGAGG[A/T]TACTGAATGCCAAGG | 10533 |
| rs542206221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353972 | CAGACTTCAAGGACA[C/G]GGTGGTTTCACTGGG | 10533 |
| rs542219032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528754 | TCACTTGAACCCAGG[A/T]GGCGGAGGTTGCAGT | 10533 |
| rs542227348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485863 | TTGTAGATATGCGAC[A/G]TTATTTCTGAGGGCT | 10533 |
| rs542239956 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11337692 | TTCTTATGTTGCCCA[C/G]GCTGGCCTTGAACTC | 10533 |
| rs542242478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347262 | TCTACCTTTAAAATC[A/G]TATGGTTTTATAAAA | 10533 |
| rs542247086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439871 | ATTTTCAGGGCGCTT[C/T]TGTACCTGCCCTTTT | 10533 |
| rs542247546 | in-del | -/A | 0.48679 | 0.0801892 | intron-variant | ATG7 | GRCh38.p7 | 3:11429948 | AGACTCTGTCTCAGG[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs542252010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295798 | TCTTTCTTTTTTTTT[A/T]TTTTTGAGATGGAGT | 10533 |
| rs542253230 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11325334 | TTGTTACTATTTGTT[A/G]AGCGCTGGCCTCATT | 10533 |
| rs542254479 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11392480 | AACAAACAAAAAAAA[A/C]AAAACAAAACAAAAA | 10533 |
| rs542283175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448316 | AGGCTCCTCCATGCT[C/T]TCCTGAGGCCACCTC | 10533 |
| rs542292965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11424114 | TCGCCTGGTCCTTTC[A/G]CTTTTCACTGCTGCA | 10533 |
| rs542300979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442777 | AAAAAAAAAATTAGC[C/G]AGGTTTGGTGGCACA | 10533 |
| rs542308918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361724 | GAGGGAAGAATACCT[A/G]CCCTGTCAACTCACA | 10533 |
| rs542325843 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11416397 | TTATAGAAATAGGCC[A/T]GTTTAGAATTTCCAT | 10533 |
| rs542336105 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11489109 | CTATTCAGAAATTCA[A/G]CTTCTTCCTGGTTTA | 10533 |
| rs542343164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310032 | TTAGCTGGGTGTGGT[C/G]GCGCCTGCCTGTGGT | 10533 |
| rs542349796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319706 | CAGAATGATGCTGCT[G/T]CTATCCAGTCACACA | 10533 |
| rs542375396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467443 | GTGCAATGGTGCGAT[C/T]TCGGCTTACTGCAAC | 10533 |
| rs542375489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11475217 | GTAACAATAATAGCT[C/T]CCATCTCTTGAATAC | 10533 |
| rs542377250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11382565 | TTCTAAACAGATGGT[A/G]TTTGTCAATGAAATT | 10533 |
| rs542378975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398273 | GAAAAGAAATACATA[C/T]TCTTTTCAAGCACAC | 10533 |
| rs542380260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535274 | CACCCTGCCTGGTGT[C/T]ATCTGAGGTGTCCTT | 10533 |
| rs542411819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11513234 | GCCTGCCAGTCCTGC[A/G]CCGTGCGTCTGCACT | 10533 |
| rs542411828 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11454188 | AAATGTACTCTAATG[A/G]GTACCTTGATTTTTA | 10533 |
| rs542414290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376044 | TTGGCAGTAAAGAGG[A/C]ATGAAATGCTGACAT | 10533 |
| rs542451235 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371655 | CCAGAGCCACTGAGC[A/G]AAAACCTCCAGGGAC | 10533 |
| rs542455363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11331177 | TCTGTAGTGCAGTGT[A/G]AGATCCTGTGGCTTT | 10533 |
| rs542460600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288023 | ATTTTTTTAAGGGTT[G/T]TAAAAAAAATAAAAT | 10533 |
| rs542464304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511066 | GAAGCTGCAGACCTT[C/T]GCGGTGAGTGTTACA | 10533 |
| rs542467251 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557994 | TGTCATCCTTAAACC[A/C]TTTGTTTTTCAGCAG | 10533 |
| rs542472809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418411 | GAGCCACTGTCCCCA[A/G]CCAACATATTTCAAT | 10533 |
| rs542473015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425880 | GCCTATTTCATTTTA[A/G]TTTTATATAAATGTA | 10533 |
| rs542478365 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11291300 | TGGCCAGGGCCTTTT[G/T]GTTTTGACTGTTGGA | 10533 |
| rs542488208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478312 | TCCCATTTTGTAAGA[C/G]CAAGGTATGAAAGTA | 10533 |
| rs542507092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11334393 | GGGATTACAGGAGCC[C/T]GCCACCATGCCCAGC | 10533 |
| rs542508272 | in-del | -/AAG | | | cds-indel, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556606 | TCTACGACAAAAAAA[-/AAG]ATCAACTTTTTTTTT | 10533 |
| rs542567983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277390 | GCCATACAGAACTCT[A/G]TCAGGGGAACCTGCC | 10533 |
| rs542572470 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297480 | GCTTTTTGGAGCTGC[C/T]AGATTTCTTTAGTAT | 10533 |
| rs542580956 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270800 | ATCAGTTAGGGTGGG[C/G]CAGAAACAAATCACA | 10533 |
| rs542583385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389037 | CAGATCACCTGAGGT[A/C]AGGAGTTCAAGACCA | 10533 |
| rs542586827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442156 | TGTTATCATCCAGTA[C/T]CATGATCGCTAGGCT | 10533 |
| rs542588417 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475604 | TGCTACCCTCTGCAG[G/T]CTGCAGATCAGCAGG | 10533 |
| rs542612803 | in-del | -/CCTC | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11500718 | TCACTGCAACCTCCA[-/CCTC]CCAGGTTCAAGCAAT | 10533 |
| rs542618433 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11401211 | CTTCCTGGGGATTCT[A/G]AAGCATGCTCAAGTT | 10533 |
| rs542622033 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11309022 | CACTGCTCTTGAAAA[A/C]CCTGTACTCCTCAAC | 10533 |
| rs542641838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11492307 | AGTGAGGCAATGCCT[C/T]GCCCTGCTTCGGCTC | 10533 |
| rs542691926 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11389519 | TGGTTAAATCACATA[C/G]CAAAGTTAGACATCT | 10533 |
| rs542698292 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352900 | GTGGTGGGAAAGGCC[A/G]GTGGCCAGGAGGAGC | 10533 |
| rs542699299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311996 | ACAGAAAATAGATTA[G/T]TGGTTGCCAGGGGAT | 10533 |
| rs542710517 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468800 | GGGCAGCCAGGGAGG[C/G]TCGGTTTCATCAGAC | 10533 |
| rs542715880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485507 | GCCTGTTCACTCTGA[C/T]GGTAGTTTCTTTTGC | 10533 |
| rs542718011 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11528400 | CCAATATCCGGGAAG[G/T]CAGATGGTCACGTAC | 10533 |
| rs542728899 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384434 | TTGACTATGCAATAG[G/T]TTCTTCTGTTGATGG | 10533 |
| rs542738968 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ATG7 | GRCh38.p7 | 3:11491591 | CTCTGTTTTTTCCCC[A/G]TCTTTGTGGTTTTAT | 10533 |
| rs542747415 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470763 | TCCCTGAAGGGCCTC[A/G]GGAACTGAGCCGAGC | 10533 |
| rs542748972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504468 | AGGGAATGGGAGATC[C/T]CACAAAGGAGAGATT | 10533 |
| rs542753428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491990 | TGTGGTGGGCTACAC[C/G]AAGTTTGAGCTTCCC | 10533 |
| rs542755563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400821 | ACTCAACCAAAATTC[A/G]TACATTACAAACGTC | 10533 |
| rs542757110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415359 | TTGAAAAACAACACT[A/G]AACTTAAAAAATATT | 10533 |
| rs542762376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396671 | CCTGTAATTCCAGCT[A/T]CTCAGGAGGCTGAAG | 10533 |
| rs542782584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300924 | AGGTTAGACGTATTA[A/G]ATAGAGTTTTGATTT | 10533 |
| rs542789778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461637 | TTAGTGGTTTTAAGA[A/C]AATGGTAATGTTTGT | 10533 |
| rs542810345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523164 | CCCAGGTTGTAAGGA[C/T]TAGTCAGAAGTCATG | 10533 |
| rs542815716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503998 | AGGCCAGAAAAAATA[A/C]GGAAGAAATTAAAGG | 10533 |
| rs542818814 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469788 | GTTCAGGAGTTTGAG[A/G]ACAGCCTGAACAACA | 10533 |
| rs542818851 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520050 | GGAAGGAGAGATCCC[A/G]TCCCATCCCCCAGAT | 10533 |
| rs542858289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516939 | AATCCACAAATTAGC[C/T]GGGTATGGTGGCACG | 10533 |
| rs542858668 | in-del | -/AT | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11436430 | CTTGAAAAATTAAAC[-/AT]AGAATTACCATGTGA | 10533 |
| rs542864901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290628 | ATTTTAGGCTTCAGA[C/T]GCACAACCTTGAAGG | 10533 |
| rs542870185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421310 | TTACCCACAGCAGAA[C/G]GTCTTTAAAAATTGG | 10533 |
| rs542876898 | in-del | -/TCTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478276 | TTCCCAGAATGAATC[-/TCTA]TCTCTCTTTTAGAAA | 10533 |
| rs542881087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340072 | AGGGCTGCGGGGAAG[A/G]GAGAAGTCAGGGAAG | 10533 |
| rs542926260 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423446 | TTGATTCCTTTGCTC[A/G]ATGCGGGGTTGCCAC | 10533 |
| rs542927213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515397 | CAACCTCCACCTCCC[C/T]GGTTCAAGCGATTGT | 10533 |
| rs542933202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395690 | TCACGCCTGTAATCC[C/G]AGCACTTTGGGAGGC | 10533 |
| rs542949029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11314657 | GAATTGGGCCAGGCA[C/T]GGTGGCTCACAACTA | 10533 |
| rs542950430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396228 | GAGGCAAGCGCATCA[A/C]TTGAGGTCAAGAATT | 10533 |
| rs542959566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11487623 | CTCCCGGACGGCACG[A/G]CTGGCCAGGCGGGGG | 10533 |
| rs542960084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428521 | TGCAGTCTTCCACTT[A/G]TGGCCAATAGTTAGA | 10533 |
| rs542963429 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11535690 | CTCTCTTTTCAACCA[-/G]GCTCCTTGGTAAAGA | 10533 |
| rs542967443 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11403614 | AATCTTCCTTTAAAT[C/G]TTATTGATAATCAAT | 10533 |
| rs542973213 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340482 | CTGTGGCAAGTCTGT[A/G]GAAATTCAGGCCCTC | 10533 |
| rs542975859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530069 | GGCTTTTTTGAGGAC[A/G]CCTCTCGGTCTTGGC | 10533 |
| rs542993666 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11502481 | TATGCGGTGTTTGGT[G/T]TTTTGTTCTTGCGAT | 10533 |
| rs543003032 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11321513 | CTGCATTTTACAGAT[C/G]AGATGAATGGAAAAG | 10533 |
| rs543016336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456131 | AGAGCAGTCATCTCT[C/G]AGTTCCCCTCACACC | 10533 |
| rs543026003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280581 | ACCTCTATGAAATTT[C/T]AAATCTTGTTAAAAT | 10533 |
| rs543026055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272947 | TTAGAAACTAATGCA[C/T]AATAAGAATCAATCC | 10533 |
| rs543029289 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11544439 | TGCCTGGGGCCTCTT[-/A]AGAGTCCAGAAGCAA | 10533 |
| rs543037806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535950 | TCCATGTGGGATGAC[A/G]CAGCGTTGCCTGCCA | 10533 |
| rs543041570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541748 | GTTGACCCCAAAAGC[C/T]CTTTGAGGTAGAGAA | 10533 |
| rs543045804 | in-del | -/AGCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11276104 | CCCATATCCTCAGGC[-/AGCT]AGCTCTCTTGTCCAT | 10533 |
| rs543048157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494450 | GTTTGAAAACTGGGA[C/G]AGTCCATTTCTGTGT | 10533 |
| rs543056854 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436648 | ATAATTGTCAAAAAG[G/T]GGAAACAATGCAGAT | 10533 |
| rs543086047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532466 | AGTGCCTCATGCCTG[G/T]AATCCCAGTGCTTTG | 10533 |
| rs543088326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11453914 | AGGTTTCTGGATACC[A/G]TAGTTGTTACCTTTC | 10533 |
| rs543128929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328270 | TATATTATTTCCTCC[A/G]TGATTAAACTGTGGC | 10533 |
| rs543149244 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11370320 | TCCAGCTTAGTTTTT[C/G]TGCCCCCTTGGTGAC | 10533 |
| rs543151695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541190 | CAGGCGTGAGCCATC[A/G]CGCCCGGCTGGTTTT | 10533 |
| rs543155560 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473339 | GTACCTGTTTTCTGT[G/T]AAGTATACCAACAGG | 10533 |
| rs543166245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399326 | CTACTCCAGCCTGGG[C/G]AAAAGAGTGAGACAC | 10533 |
| rs543167214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11320633 | GATTAATATATTTTT[C/T]TCCCATTTAAATGTA | 10533 |
| rs543172733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308599 | TCTCTATCTAGACTG[C/T]GAGTGTCTTGAGGGT | 10533 |
| rs543173192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526258 | TAGCCGGGCCTAGTG[A/G]TGCATGCCTGTAATC | 10533 |
| rs543205730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11341540 | GCAACCTCTGCTTCC[C/T]GGGTTCAAGTGAATC | 10533 |
| rs543214189 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498100 | AGTTAAATCCTGACT[C/T]TCAATCCAGTATTCT | 10533 |
| rs543220871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311318 | CTTAGAATTCGTGAG[A/G]TCCGGCCGGGTGCAG | 10533 |
| rs543222645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444166 | TTCATTTTCGTTGCT[A/G]TGTAGTGTTTCATAA | 10533 |
| rs543234689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348573 | TAAGAATGAAGCCAC[A/G]GACGTTCGCATGTTA | 10533 |
| rs543251181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11479465 | ACAAAATCCAAACAT[C/T]GTAAAGTTACTTCCA | 10533 |
| rs543258940 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340942 | ACTCTTCATCTGTTC[C/T]AGACATTCTAAATTT | 10533 |
| rs543269097 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338494 | TTCCCCACAGAAAAA[C/G]AATTCTGAAGTCTTA | 10533 |
| rs543271654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349216 | TGGTGCATTTACAAT[C/T]CTCTAGCTAGACAGA | 10533 |
| rs543292611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527157 | TTGTCCAGGCTGGAG[C/T]ACAGTAGCACGCTCT | 10533 |
| rs543297808 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11486562 | TACCCTGGCCAGAAC[G/T]TCCAACACTATGTTG | 10533 |
| rs543298127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355914 | GTCCATAGCACCTTT[A/G]TTCAAAACAGCCCAA | 10533 |
| rs543304018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408699 | TACAGGGGAACGCCT[C/T]GTTAAAACTGCCATA | 10533 |
| rs543304699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367810 | CGTGGATTAGATTCT[G/T]CAAGCAGGCAGCAGT | 10533 |
| rs543308635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450362 | TCACGTGTTTGACCA[C/T]GGTTTTCATGTTCTC | 10533 |
| rs543331146 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278835 | GGTAAGGTAGTTGGT[G/T]CTCTTTGAGGACTAG | 10533 |
| rs543334497 | snp | A/G | 1.66214e-05 | 0.00288278 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315387 | ATCTTTGTCAAACAG[A/G]AGGAGTCACAGCTCT | 10533 |
| rs543348025 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11489995 | ATGTCTATTAGGTCC[A/G]CTTGGTGCAGAGCTG | 10533 |
| rs543367438 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11281236 | CAAAGGGGGTTCCAT[A/T]TATATCATAGGTATC | 10533 |
| rs543378914 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11398316 | ACAAGAATTTGCTGG[A/C]ATAGACGGGATAATT | 10533 |
| rs543380769 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315393 | GTCAAACAGAAGGAG[G/T]CACAGCTCTTCCTTA | 10533 |
| rs543382220 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372900 | TTGTGGGGAGAGGGG[A/C]GAATGAGAAAACAAT | 10533 |
| rs543382652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318248 | AGGAAAGCCTGGAAT[C/T]ACTCAGCACACGTGA | 10533 |
| rs543389288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297914 | AGGAATAACAGTAGT[A/G]CATCAGTCAGACTGA | 10533 |
| rs543416468 | in-del | -/TT | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11471693 | CACATATTCCAACTC[-/TT]TTTTTTTTTAGAACT | 10533 |
| rs543420816 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11366874 | CTAGTTCTTTCTCCT[A/C]GTTTTCAAATGTCTG | 10533 |
| rs543436370 | snp | A/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11547905 | GAGTGTAAGTGGCAT[A/G/T]GTCATGGCTCACTGT | 10533 |
| rs543436664 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11458312 | TGTGTTGCCCAGGAT[G/T]GAGTGCAGCGGCACC | 10533 |
| rs543438986 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424203 | CAGTGCCAACCTCTT[C/T]ATCAGTGCTTTAGAG | 10533 |
| rs543439416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11411568 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 10533 |
| rs543448265 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501017 | TTCAGCACTTTGGGA[A/G]GCCAAGGTGCGAGGA | 10533 |
| rs543458617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11426684 | TAGATTGCATTATTA[C/T]CCCCATGTTTAATTC | 10533 |
| rs543458883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332221 | GAGTGAACTATTAAT[A/G]CAGAGATCAGCATGG | 10533 |
| rs543466685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432942 | CCTTAAAGCTGATGA[A/T]CCACAGGGTGTCCAA | 10533 |
| rs543478633 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426000 | ACTATACCACAATCC[A/G]TTTGTTCATTCTACT | 10533 |
| rs543480410 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11538842 | ATTGTGCCACTGCAC[A/T]CATACTGGGCAACAG | 10533 |
| rs543493516 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312118 | ACAACCATATCACTA[C/T]ACTAAAAAGAAACCA | 10533 |
| rs543506342 | snp | A/C | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450894 | CAATGAATGCCTTCC[A/C]AAGGGCTGGTGTCCT | 10533 |
| rs543521802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330457 | CAGCCTTGGCTATTG[A/G]TAACTCTTACAGTTG | 10533 |
| rs543525742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11426057 | GTTTTGGGCTATCAT[A/G]AATAGCGCTGCTGTG | 10533 |
| rs543528677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418212 | CGGGTTTAAGCCATC[C/T]TCCCACCATAGTCTC | 10533 |
| rs543537606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484955 | TCGTTGTTGGACAGT[C/T]GGGTTGGTTCCAAGT | 10533 |
| rs543538730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464990 | ACATCTATCATCATC[A/G]TCATCAACAATCACA | 10533 |
| rs543550718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11297302 | GGCTGAGGTTGCAGT[A/G]AGCTGAGATTGTGCC | 10533 |
| rs543551883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345746 | TTTGCTTTCAGATTC[A/G]TAAATATCTACTTTT | 10533 |
| rs543554166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543683 | GGTGGGCGGATCACC[C/T]GAGGTCAGGAGTTGG | 10533 |
| rs543554442 | snp | A/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450514 | AGGTCACAAGAGATC[A/G]ATGTACAAATGAAGC | 10533 |
| rs543556378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324202 | TCGCACAATTAATTT[A/G]TGGCAAAGCCAGTTC | 10533 |
| rs543580651 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11402022 | GTACAACTTGGTGGG[-/T]TTTTTTTCACATGTA | 10533 |
| rs543582182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393906 | GGCTGGTCTCAGACT[C/G]CTGAGCTCAAGCAGT | 10533 |
| rs543582196 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11302574 | TGTATGAGAGAGAGA[A/G]GTAGAAGGCAAATAT | 10533 |
| rs543598894 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478438 | AGAGATGAGACTGGC[G/T]CATATTAAAGATGCC | 10533 |
| rs543605956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453370 | GAAAGATAATACTAG[A/T]AAACTCAGAGGGATA | 10533 |
| rs543617518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453856 | AAGCAGGCATGGAAA[G/T]CCACCAACAGTGTGC | 10533 |
| rs543631229 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11352016 | CTCCCTCCACGCCAC[A/G]ACAGGCACTTGTGTG | 10533 |
| rs543635016 | in-del | -/TAAT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11336583 | TGTAAACTGAAAATA[-/TAAT]TAAGTATGGTTGTAC | 10533 |
| rs543647825 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11419427 | GGAATGGTGGTGTGC[A/G]CCTGTAATCCCAGCT | 10533 |
| rs543651357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11459967 | CTGTGCTCTTATCCA[C/T]TGCACCATACTGCCT | 10533 |
| rs543654589 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311762 | TTAGGACTCATAGGA[C/T]TAGACAGTTCATTAA | 10533 |
| rs543681148 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455989 | GCTTTATTTAGATGT[A/C]ATTCATATGCCCTAC | 10533 |
| rs543687270 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11405820 | AGATGGGGTTTCGCT[A/G]TGTTTCCCAGGCTGG | 10533 |
| rs543692541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359057 | ATGCCACATTATATT[A/G]AATAAGGAAGATACA | 10533 |
| rs543709463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11490426 | TTGACTCTTTATCCA[A/G]TTTGCCAGTCTGTGT | 10533 |
| rs543709514 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11320454 | ACCACACCTGGCTAA[-/T]TTTTTTTATCTTTAG | 10533 |
| rs543716787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539710 | ATATTCGTTTTCTCT[C/T]ATGAATTTAAAAAAT | 10533 |
| rs543716841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545574 | TGACCTAGGACTTCA[C/T]GGACCAAGCCCTAAC | 10533 |
| rs543721053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326605 | ACCCGGCCTAGAGTT[A/G]TAAATGCTTTTTATG | 10533 |
| rs543721494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551932 | TTTTGGATTTTTAGT[A/T]GAGACGGGGTTTCAC | 10533 |
| rs543723853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533091 | CGGAGGTGCGCTGGT[A/G]CGCAGAGCAGACAGT | 10533 |
| rs543729220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420708 | ATTAAGTGTGCAATA[A/G]CATTATGTCTAAAAA | 10533 |
| rs543731324 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11310784 | ACTACAGGCACCCAC[C/G]ACCACACCCGGCTAA | 10533 |
| rs543734515 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11552401 | TGATCTTCACTAAGA[A/G]GACATTCACTGTGCC | 10533 |
| rs543736269 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11299480 | CAAGGAATAAGCATG[A/C]TTGCCTCCCTCATAG | 10533 |
| rs543770664 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11554215 | GACACGCATTGAGGG[A/G]CTGTGGCAGGATCTG | 10533 |
| rs543773370 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11367986 | TCAGAACAAAGTAAC[C/T]ATCAAGCACCTTCAA | 10533 |
| rs543781418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11301475 | CTCAGAAAATCAATA[C/T]TTTTTTTCCCTTTAT | 10533 |
| rs543787789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429569 | CTGGGAACTCCAGAC[A/C]TGCATCTCTTAATAG | 10533 |
| rs543793678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466895 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 10533 |
| rs543796739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472887 | TTCTTGATAAGATCA[C/G]GGAATCCTTAAAATT | 10533 |
| rs543802849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380599 | GATATATCTCAAAAC[G/T]ACAGTGATGGCATCT | 10533 |
| rs543804662 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557241 | TATTAATATAGCAAA[C/T]AATAAATGCAGTAAT | 10533 |
| rs543808416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11282473 | CATCATAGCAATTTT[C/T]CTAACTGCCAGTGTG | 10533 |
| rs543820918 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11288863 | CAGCCCCGGGGGATT[G/T]TATTGGTTAACCACA | 10533 |
| rs543831513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516893 | TTCAACAACACCCTG[G/T]CCAACATGATGAAAC | 10533 |
| rs543837779 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11491837 | TTCCTCTGGAAGTTT[C/T]GTCTCAGAGGAGTAC | 10533 |
| rs543848126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429971 | AAAAAAAAAAAAATT[C/G]TGTGAAAAGGATATC | 10533 |
| rs543862867 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11306625 | ATTCAAACTGTGCAC[A/C]GCTCAACAAACAATA | 10533 |
| rs543868591 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11296553 | CCCTTTACCCACTGC[A/G]GAATCATATTTACCA | 10533 |
| rs543868671 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464825 | CTGTGTGACACCTTG[A/G]GCAAGTTGCAGAGTC | 10533 |
| rs543884347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523117 | TTGGGTGTTTGTATT[A/G]TAGCCCAATCCAAGT | 10533 |
| rs543889874 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533528 | ACCACAGAGAAAAAT[C/T]CCCCTTCTGTTAAAA | 10533 |
| rs543922505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386952 | AAAAACCTTGGACAT[C/T]TCTCCCTTTGCTTCT | 10533 |
| rs543935024 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556498 | GTTTTCCTGTTACGA[C/T]GCTCAGTAGCCTGTA | 10533 |
| rs543937468 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11323560 | ATTAAAAATAGCTCA[G/T]AACATTGTCCCATTA | 10533 |
| rs543945658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348549 | GTGGGTTCATAGTCT[C/T]GCTGACTTTAAGAAT | 10533 |
| rs543949273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319158 | AAAGAAGGCTTTTGC[C/T]GGGGGCAGGGCCGAA | 10533 |
| rs543974307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341237 | CTGCTAATTTTTTGT[A/G]TTTTAGTAGAGACAG | 10533 |
| rs543994723 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11415512 | AGCCATACAAAAACA[-/T]TTTTTCTTTATACCC | 10533 |
| rs544006848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11276003 | TGGTAACCTAAAGCC[C/T]TGCCAGCTCCATTAT | 10533 |
| rs544015067 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516580 | CCTTGAGATTTACCC[A/G]AATTAGTTGATAATA | 10533 |
| rs544026127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322909 | TTCAAGACCAGCATG[A/G]GCAACATAGCAGGGC | 10533 |
| rs544031392 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11534716 | TCAACCCACAGTGGG[A/G]CGCTGCTCCCTCCCA | 10533 |
| rs544042056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275426 | CGATCTCGGCTCACT[A/G]CAAGCTCTGCCTCCT | 10533 |
| rs544050673 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271714 | CTTGTGAGGATTAGA[C/G]ATGTAAAACCCTGAA | 10533 |
| rs544053978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420171 | AAATCCTTGTACTTT[G/T]TGTAAGCCACTTATA | 10533 |
| rs544062566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496514 | CTTCTCTGAGGGCTG[C/T]TGAGGCTGGGACTTT | 10533 |
| rs544065495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11547701 | TGATCTGGCTTTTTC[A/G]CTGCAGCCATCCTAG | 10533 |
| rs544066589 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11406508 | AGATGACATCTTGCT[A/T]TATTGCCCAGGCTGG | 10533 |
| rs544075981 | in-del | -/TGCTCTTAC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466644 | CTCTGTAAGCCTTTG[-/TGCTCTTAC]TGCTCTTTTCGGAAA | 10533 |
| rs544078210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335770 | TGGCACGATCTCGGC[C/T]CACTGCAACCTCCGC | 10533 |
| rs544082280 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11373459 | CATCCTGTTTCCCTT[A/G]CTTGCCTGATGGGAA | 10533 |
| rs544103409 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11418899 | AGAGCAAAGGGGGAA[A/G]TGCCACTTTTAAATC | 10533 |
| rs544111171 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441363 | TTCTCTACCTCAACC[A/T]CCCGAATAGCTGGGA | 10533 |
| rs544118433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413119 | TTTGCAAGCAGAAAT[C/T]GTTTTACTTCTTCCT | 10533 |
| rs544121130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11502559 | GGACGTGAACTCATC[A/T]TTTTTTATGGCTGCA | 10533 |
| rs544128628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459213 | ACATCAGTCATTATG[A/G]TGAAATGTCAACACA | 10533 |
| rs544129462 | in-del | -/ACT | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11407980 | TAGTTACTTAAGCAA[-/ACT]TCTGCAGCTGGCTTG | 10533 |
| rs544140357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422865 | GTTTAAGTGATTCTC[C/T]TGCCTCAGCTTCCCA | 10533 |
| rs544147466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495967 | TTCATAGGCGCGTCA[C/T]GCTAGCATTTCCAGG | 10533 |
| rs544160794 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11293933 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGGGAGG | 10533 |
| rs544160960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475819 | CTAAGTAGGCAGTTG[A/G]TATTATTTCTTAACT | 10533 |
| rs544163029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11390365 | CTATTGGAGGAGCAA[A/G]AGTTTCATTTAACAA | 10533 |
| rs544165809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374628 | AAGCACAAAAAGTCC[A/T]TGTGTGGTGGCTCAC | 10533 |
| rs544194403 | snp | A/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11383304 | GATATTTTGCCAGTT[A/T]TTTTTGTAGAATTTC | 10533 |
| rs544199172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357724 | CAGTTGGAAAGAGGT[A/T]CTTTGGCAGGGTACG | 10533 |
| rs544202347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416253 | TCCCTTTGCTTCTGT[C/T]TTCTGAAAGAGATTG | 10533 |
| rs544208035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293332 | GTCAGGAGTTTGAGA[C/G]CAGCCTGTCTAACAT | 10533 |
| rs544226837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11279869 | CAAATTGCTATACTC[C/T]GATTCCTCTTCTGTT | 10533 |
| rs544233711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397546 | CACTGTAGCCTCCAT[C/T]TCCCAGGTTCAAATG | 10533 |
| rs544235485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358272 | TGAAGAAGAGAGAGG[C/G]CGTGGGAAGGGTGCA | 10533 |
| rs544237234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11350363 | CACACAATCCCAAAA[C/T]CTCAGTGGCTTACAA | 10533 |
| rs544245256 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11514105 | AACACATGACTGTCT[C/T]ATCTAATCCTGATAA | 10533 |
| rs544289336 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11438585 | AAAACAAAACAAAAA[A/T]AAAGATTTTTTTTCT | 10533 |
| rs544306308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349169 | TAGCTAGACACACAG[C/T]GCTGATTGGTGCGTT | 10533 |
| rs544331775 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451014 | TGTACCAAATACAGT[A/C/G]ATTATGGCACAGGAA | 10533 |
| rs544360694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478274 | TTTTCCCAGAATGAA[A/T]CTCTATCTCTCTTTT | 10533 |
| rs544373859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315551 | AAAAATCTGAAGTTC[A/C]TGTTACAAGAGACCA | 10533 |
| rs544377975 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11493236 | TCAATTTGCCTCTCT[C/G]CCCCTCTTCTCCAAA | 10533 |
| rs544393904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530778 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 10533 |
| rs544398518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378174 | GTGCACCACCACACC[C/T]GGCTAATTATTTTGT | 10533 |
| rs544406986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379181 | TAAATTAATTCATAA[G/T]ATTTGTGTTGTCTGG | 10533 |
| rs544407312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385681 | AGGACTAGGGAAGGC[C/T]TTGCAGAGGATGACT | 10533 |
| rs544411529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371860 | TGCACATCTGCAGCC[C/T]CAACAGGTGTTCCTG | 10533 |
| rs544430275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278206 | GAGGTGACTTACATT[A/C]TCAGCTTACAAAGAT | 10533 |
| rs544431623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416838 | ATATTATTTCAGTGA[C/T]ACAGATTTCTGTCTC | 10533 |
| rs544445436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511942 | CAGCTGGCCTGCAAG[C/T]GCCGCATGCAGCCCT | 10533 |
| rs544452770 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11499662 | TGAGGCAGGAGAATC[A/G]CTTGAACCGGGAAGG | 10533 |
| rs544454502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408902 | ACAGGTGTGAGCCAT[C/T]TTGCTGGCCAGAGCA | 10533 |
| rs544457037 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11522924 | CAGCCCGCCACCTAC[C/T]AGCCGCATGACCTCA | 10533 |
| rs544484285 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272071 | TGGCCCCTGTGCTGC[A/G]TTTGATGCCGCCTCT | 10533 |
| rs544486072 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11506904 | CCATTCCCTAGGTAA[A/G]GATTCATAGCATTTT | 10533 |
| rs544500633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464477 | CCCCTCGGTAAAGTA[C/T]GGGGGGAGGCTGAAC | 10533 |
| rs544546275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11531529 | GCAATCACATGGTCC[A/G]CAAGTCTGCATATTG | 10533 |
| rs544546643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505866 | TGGAGGCATTCAGAG[A/G]GCTGAAAGGTACACA | 10533 |
| rs544547932 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395668 | TGAAAGGGCTGGGTG[A/C]AGTGGCTCACGCCTG | 10533 |
| rs544553360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477788 | TGGGAATCAGTACAG[C/T]CTAGACGCATTCTCT | 10533 |
| rs544558876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377453 | CCTGTGGTGGTGTTG[G/T]TGTTTTTCTTCTCTA | 10533 |
| rs544566726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11489063 | TGGTAAGCTATTGAT[G/T]ATTGCCACAATTTCA | 10533 |
| rs544577766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485093 | CAAATGGTATTTCTA[A/G]TTCTAGGTCCCTGAG | 10533 |
| rs544601129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445284 | ACTATTCACAATAGC[A/G]AAGACATAGAATCAA | 10533 |
| rs544618283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309766 | GTATATATATCTGTG[C/T]ATATAAAACTAATTT | 10533 |
| rs544619168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11294764 | ATCCCTTCTCTTATC[A/G]AATCTTCTTTCCTCC | 10533 |
| rs544620098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302922 | CTGTCTTAAACTGGA[A/G]TATGCTGTCTTGAGT | 10533 |
| rs544652045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491539 | TTCCTTTGGAGGAGG[A/G]GAGGCGCTCTGCTTT | 10533 |
| rs544654399 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11365153 | TGACATCACCTGGTA[G/T]TTGTATGGATTATGG | 10533 |
| rs544656999 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524860 | CCCCATTGTCCTGTC[A/G/T]TCCTCCAGGTGAGGT | 10533 |
| rs544658797 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11354089 | TAACCGTATTCTGGC[C/T]CCAGACCTTCCAGTA | 10533 |
| rs544658984 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367726 | TTTGAAAACCATAAA[C/G]CATTTCAGGTGAGCT | 10533 |
| rs544659063 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331489 | TATATGTTTTACAAT[A/G]TGTCTGTTTCTATTT | 10533 |
| rs544668101 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348509 | TGTGTCTGGAGTTTG[C/T]TCCTTCAGATGTGTC | 10533 |
| rs544686853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448178 | TGAGGCTTTGAAAAA[A/C]TTAGCTGCACAGTCT | 10533 |
| rs544688180 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298083 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 10533 |
| rs544697629 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11340064 | ATTAAAAGAGGGCTG[C/T]GGGGAAGGGAGAAGT | 10533 |
| rs544705647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11537618 | TAAAACAAACTACAC[A/G]TGCAACACGAACTCC | 10533 |
| rs544726658 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11403371 | AAGGGTATTGGGGGA[A/G]GGTAGTAAGGAGAAG | 10533 |
| rs544757684 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11396434 | ACAGAGCGAGACTGT[A/C]CCAAAAGAAAAAAAA | 10533 |
| rs544767408 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555269 | TGCTGCCCACCGCAC[C/T]GCAGGCTCCTCCTGT | 10533 |
| rs544767510 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499375 | CAGATTGAACTAATG[G/T]TGAAGCTGTGACCCA | 10533 |
| rs544769794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326475 | GGCTAATTTTTTGTA[G/T]TTTTAGTAGAGATGG | 10533 |
| rs544770790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480873 | CCTCTCTTCTTCCCA[G/T]TCCAGCATTAGACTT | 10533 |
| rs544782893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518822 | CACTGAATTCTAACA[A/G]TTATTTCTGAAAGTA | 10533 |
| rs544796915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512447 | CATTGCACAGGATTA[A/G]TGTTCCATCTCAGAT | 10533 |
| rs544802278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431347 | TGGAGGCTGCAGTGA[C/G]CTGAGATTGTGCTGT | 10533 |
| rs544811338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471080 | AGCGAGCCCAGCCCT[G/T]AGTCTCTGTCCCCTC | 10533 |
| rs544812659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381839 | GTATTTCCTTACAGT[A/G]GAAACGCAGCATTTA | 10533 |
| rs544814398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275411 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 10533 |
| rs544828799 | in-del | -/GC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534205 | CTGGAGATTCCAGCA[-/GC]GCACCCTAGGTCTAG | 10533 |
| rs544846366 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11534877 | AGGCTCAGCCCAATG[C/T]GCTTCAGGCCCACGT | 10533 |
| rs544862138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439313 | ACCTCAAATGATCTG[C/G]CCGTCTCAGCCTCAG | 10533 |
| rs544863289 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557806 | ACAAACTGCAGTGTT[C/T]AGAGAAGATAAAATG | 10533 |
| rs544865153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431913 | CCAAGCTAGAATCAT[C/G]TAGATTTAGTGAGAT | 10533 |
| rs544874388 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11417108 | AGAATGTTCTACCTT[-/G]GTGAATATTCCATGT | 10533 |
| rs544877690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515367 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 10533 |
| rs544880808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398138 | TAATTGATGAAAAAA[A/G]GATACCAAAAGAAAT | 10533 |
| rs544888080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485459 | CTTCGTCAGATGAGT[A/C]GGTTGTGAAAATTTT | 10533 |
| rs544898785 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11333809 | CTAGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 10533 |
| rs544918049 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11391962 | ATTGTACTTATTGGG[C/G]GGGGGGTAATTTCAC | 10533 |
| rs544935025 | in-del | -/A/AA/CA | 0.047962 | 0.147477 | intron-variant | ATG7 | GRCh38.p7 | 3:11427814 | GCGAGACTCCGTCTC[-/A/AA/CA]AAAAAAAAAAAAAAA | 10533 |
| rs544946255 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11444272 | TTCTGGTATATATCT[C/G]CTGGGGTTCATGTGC | 10533 |
| rs544949252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480482 | TGGGAGGGGGTGCGA[C/T]GGTTTGCGGCAGGGG | 10533 |
| rs544958971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400141 | CTTTCAGAGAATGCT[C/T]ATCCCAGCTTGAAGG | 10533 |
| rs544961903 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11303636 | TCCTGCCACTGCACT[C/T]CGGCCTGGGCGACAG | 10533 |
| rs544972089 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527314 | TTCGCCATGTTGGCC[A/G]GGTTGAACTCCTGAC | 10533 |
| rs544979752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11276856 | CTCATGACCCCTGTT[C/T]TGTATCATAGCCCGA | 10533 |
| rs544984109 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11527689 | GTTTGAGAAAATTCT[A/C]TCCTAGAAAGGATTT | 10533 |
| rs544985692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447703 | TAAGAAATCTTTCCT[A/G]GTGGCTCCAAAAAGA | 10533 |
| rs544986582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311989 | CACAGAGACAGAAAA[C/T]AGATTAGTGGTTGCC | 10533 |
| rs544990707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11406940 | TATCATTCTGGCCCC[A/G]TCCCTCTCAAATTTC | 10533 |
| rs545001257 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11307496 | GCAGTGTCTTCACTT[A/G]TCTACTGCATCTGAT | 10533 |
| rs545014888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283997 | AAAAAACTAAAACAC[A/G]CAGAAAAATCAGAGT | 10533 |
| rs545014913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11276315 | TTAAGACTAAGTCCT[A/C]TATTTGTGCTTGAGA | 10533 |
| rs545024278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11312909 | CTTGCCATCTTTTTT[C/G]TTGTTGTTTAGGTTT | 10533 |
| rs545030938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441596 | TAGAGGTAACTGTTA[C/G]AAGTTTCTGTACCCA | 10533 |
| rs545035756 | in-del | -/TTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334245 | GCACTTTCACAACAT[-/TTA]TTATTATTATTATTA | 10533 |
| rs545066072 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11295921 | GTAGCTGGGATTACA[A/G]GCATGTGCCACCACA | 10533 |
| rs545077473 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390017 | GCTCTTCCACAAAGG[A/G]CCTTGAAGGGAGAGG | 10533 |
| rs545081410 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519751 | CATTTTTAGTAGAGA[C/T]GGGGTTTCACAGTGT | 10533 |
| rs545086288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11495928 | TCATGTGCACCGTAA[A/G]GACTTATACTATATT | 10533 |
| rs545096246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370305 | TAACACTGGCTCATG[C/T]CCAGCTTAGTTTTTC | 10533 |
| rs545098320 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11541175 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCATCG | 10533 |
| rs545100159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278643 | TCCTTTCTCATAGAA[C/T]TTTTATTTATTCATT | 10533 |
| rs545117472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453274 | AAGGCCTGTCCCCAA[A/G]CTTTAGTAACTTTTT | 10533 |
| rs545133744 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466768 | CATCAGAATGACAGC[-/T]TTGTAGTACACTCAT | 10533 |
| rs545142498 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523316 | GTTTTAAGTAATGCT[C/T]ATAAAATTCTTAGCC | 10533 |
| rs545148621 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11529566 | TCATGAGGGAGACTT[A/G]TTAAATACTTGGAAG | 10533 |
| rs545149028 | in-del | -/AAAAAAAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374911 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GTCTGGGCATGGTGG | 10533 |
| rs545151404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474632 | AAGAAAGAAAACAGA[A/G]TGTTTGGATGAATTG | 10533 |
| rs545154276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473908 | CAATTTCTGTGCATA[C/T]GTTCAAACCTCAGGT | 10533 |
| rs545161771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510556 | CAAAGCTGTCCCCTC[A/G]CTCTTTGTGCAACTC | 10533 |
| rs545167286 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493303 | CTCTGAAGGCAAGTC[A/G]CCTCTCCCCAACATC | 10533 |
| rs545190784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509902 | GGTCTTGTGATTCAG[C/T]CCAGGATCCTGATAG | 10533 |
| rs545196499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368173 | AGAGGGAACTTTTTC[A/G]TTATAAATCTTATAG | 10533 |
| rs545199766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11307915 | GGTCGTTTTTCTTGA[C/T]CTGTGGCTTGACTGC | 10533 |
| rs545236279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530031 | ACAGAGGAGGACCTT[C/T]TACTTGGATCAGAGG | 10533 |
| rs545250953 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400184 | GAATTTCCAATTAGT[A/G]GAGGTAACCTGCTGG | 10533 |
| rs545252349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310998 | AGTTACTTGAACGTC[A/G]GTACGCTTTCTGTAC | 10533 |
| rs545257518 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551812 | GGAGTATAGTGGTGC[A/G]ATCTCAGCTCACTAC | 10533 |
| rs545265433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340006 | ACTTTGGGAACTGCT[A/G]GAATTGGAGTTAATT | 10533 |
| rs545267893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449848 | GTTGTAGATGGAAAA[C/T]GCATTAACTGCTGAG | 10533 |
| rs545281123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394263 | AAGACCATGTACTAA[A/G]GATATATTATATAAC | 10533 |
| rs545282340 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11439234 | CACCACGCCCGGCTA[-/T]TTTTTTGTAGTTTTA | 10533 |
| rs545293547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407600 | TACAGCAAACTTCAG[C/T]CTGGGCATCCAGGTG | 10533 |
| rs545303523 | in-del | -/AC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478990 | GCCTGTATATTTACA[-/AC]ACACACACACACACA | 10533 |
| rs545305718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11408160 | TCTTCTGCCAGATAC[C/T]CTAAATCATCTCTCA | 10533 |
| rs545320699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313846 | CTCAAGCAATCTGTC[C/T]ACCTCAGCCTCCCAA | 10533 |
| rs545327369 | in-del | -/TA | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527007 | GGTATATTAAATTAC[-/TA]TATATATAGTATATA | 10533 |
| rs545360280 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11306452 | AGATTGATTAGAGCA[C/G]GACCTTGAAGCCTGG | 10533 |
| rs545368547 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11502547 | TGTCCCTACAAAGGA[C/T]GTGAACTCATCATTT | 10533 |
| rs545373791 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450566 | CATTCTCCATAAGTA[C/G/T]ATGGGAGACAACTGA | 10533 |
| rs545405824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507526 | ATAAGTATAATGTGA[C/T]ATGAAAATACCTATA | 10533 |
| rs545408850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546821 | TCCATTGCAGGGCAG[C/T]GGCCAGTGGGGAGCG | 10533 |
| rs545409773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287290 | AGGAGTATGAGGGGA[A/G]TGAAGACAGGCGAGG | 10533 |
| rs545413661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537990 | TCTGGCCCTGAATGT[A/G]GAAGAGGCCAGGGAA | 10533 |
| rs545422250 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475385 | GTTCTGAGCATTCCT[C/T]AGTGAGGAAAGGGAA | 10533 |
| rs545428206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11417649 | ATTGGTACATTCAGA[C/T]CACTGATTATTGATA | 10533 |
| rs545435880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454922 | GGACAAACTCAAACC[C/T]TGCCTCCCAGAAGCT | 10533 |
| rs545463428 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11466956 | CTAACATGGTGAAAC[C/G]CCATCTCTACAAATA | 10533 |
| rs545480647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11428349 | AGTATAGGAAGACCA[C/T]GTAGAAATACCAAAG | 10533 |
| rs545482483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511920 | AGCCCACACCCACCC[A/G]GAACTCCAGCTGGCC | 10533 |
| rs545487256 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515502 | AGAGACGGGGTTTTG[C/T]TGTGTTGGCCAGGCT | 10533 |
| rs545494059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500462 | TACAACTAAAAAATA[C/G]AAATTAAAAGACTAA | 10533 |
| rs545496124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278905 | AGGGAAGGCTTCCCT[C/T]AGAAGTGATGATTGA | 10533 |
| rs545498931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333561 | CTTATGTGACAGTTA[C/T]CAGCTTTTACCCCCA | 10533 |
| rs545501806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327585 | TTTGAGAAATTGCTG[C/T]AGACAATCAAGAAGT | 10533 |
| rs545508283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537885 | GTGGCTGGTAGAGCC[C/T]GGATCCAAAATTGGG | 10533 |
| rs545519216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11506773 | AAAAAATGCTTCCAT[C/G]ATCACAGAAAGTTTA | 10533 |
| rs545519479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546279 | CGGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC | 10533 |
| rs545530213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551798 | CTGTCGCCCAGGCTG[G/T]AGTATAGTGGTGCGA | 10533 |
| rs545530453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375425 | ACATTACCAGTCATT[A/G]GAGAAATGCAAGTCA | 10533 |
| rs545538972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423551 | CAGTGGACATTTTTT[C/T]CTGACGTAACATTCT | 10533 |
| rs545539413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11384962 | ATGCCCCAAAACCCC[C/T]GCCAGAAAGAAGCAT | 10533 |
| rs545549493 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11532373 | GGAGGACAGAGCTGA[G/T]TCTGGAAAGAGGAGG | 10533 |
| rs545561490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11469756 | TTTGGGAGGCTGAGG[C/T]GGGGTAGATCATTTG | 10533 |
| rs545573268 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11360954 | TGAACCTTGACTGGC[A/G]TCATCAACTGTACAC | 10533 |
| rs545582813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11390335 | TAAGAAAACAAAAAC[A/G]TGTGTCTCCCAGCTC | 10533 |
| rs545585555 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11524723 | GCCCACAAGTTGGAG[G/T]CTGCAGTGAATTATG | 10533 |
| rs545617695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354788 | CCATAAACAATTACA[C/T]GCTGGGACAAAATAC | 10533 |
| rs545617764 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11384954 | TCATGCCCATGCCCC[A/C]AAACCCCCGCCAGAA | 10533 |
| rs545626862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295561 | TTTTAAGCAATCTAC[A/C]ATGAAATTGCATTTT | 10533 |
| rs545635726 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11533035 | AGCAAGCCCCAGCCT[C/G]AGCGGGAATGACTGG | 10533 |
| rs545644528 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11370599 | TCCAGTTGTGGCTGC[A/C]ACTGTGCTTTCTCAG | 10533 |
| rs545645226 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11357226 | TCTAGAACACATTTT[C/T]TGTGGAAAGTCAGTG | 10533 |
| rs545676983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362450 | CTTTTCAAATCATTG[C/T]TCCTTTCTGTGTCTC | 10533 |
| rs545677505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11415318 | TGACTGTGAAGGTCT[A/G]GGACATTTTGTACAC | 10533 |
| rs545681965 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438865 | TTCACATCAGCAGTG[G/T]AGGCTTCCCTGGGAG | 10533 |
| rs545684224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273592 | TTGTCATGTTTTGTT[A/G]TATCCCCAGCATATA | 10533 |
| rs545699415 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308558 | CAAATCCTACATGGT[C/G]GTGAAGTTATACATT | 10533 |
| rs545714117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321363 | AGTGGGTACCTGCCC[C/T]TGAAGAGGACACATT | 10533 |
| rs545737057 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | ATG7 | GRCh38.p7 | 3:11372843 | GTGTGTGTGCGTGCG[C/T]GCGTGTGCGTGTGTG | 10533 |
| rs545738660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330373 | ATCAGTGTGGACTCG[C/T]AGATACTTATTTTAT | 10533 |
| rs545738679 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11345757 | TTCGTAAATATCTAC[-/G]TTTTATCTTTATTAA | 10533 |
| rs545756352 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11314242 | ATAATCAGGCTGGTA[G/T]AACAGAGACCCTAAA | 10533 |
| rs545765436 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11379034 | CAGAGAAGCTCAGGC[C/T]GGGGGCAGGTTCACA | 10533 |
| rs545773025 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11348309 | CAAGAATGAAGCCGC[A/G]GACCTTCGCAGTGAG | 10533 |
| rs545776728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440748 | GAGTGCAATGGTGCA[A/G]TCTTGGCTCACTGCA | 10533 |
| rs545778613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432140 | GACAAAGATGAATTG[A/T]TTTAGGTAGTGATGA | 10533 |
| rs545784381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11404070 | TGGATTAATTGGTCA[A/G]AGCATCCATTTAAAC | 10533 |
| rs545808334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372405 | TAGGGTTTTCATTTC[A/G]TACTTTTCTGCAGTG | 10533 |
| rs545811769 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549699 | AAGACTGCTGCGGAC[A/C/G]TTCTGGCTCAAGTTT | 10533 |
| rs545812261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11543564 | AAGAGTGGGAAGGCA[A/G]GCGGGTGTCTTTCCA | 10533 |
| rs545829950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11457805 | ATGAACACCTAAGAG[A/T]CTGTGCAGTGGTAGC | 10533 |
| rs545841462 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11415348 | CCACTGTAGCCTTGA[A/T]AAACAACACTAAACT | 10533 |
| rs545843133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431282 | GGCATGTGCCTGTAA[A/T]CCCAGCTACTCGGGA | 10533 |
| rs545865232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477723 | TGTTACTGGAACTAC[C/T]CATAGGATTACAGGA | 10533 |
| rs545867037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440018 | GGCTGGAATCAGAGA[G/T]GAAGAAGTGCATAGG | 10533 |
| rs545887074 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554898 | GCTGAGGAGCTCTCC[A/G]TCGCCAGAGCAGGAC | 10533 |
| rs545888681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11297209 | GAAAATACAGAAAAA[A/T]TAGCCAGTCACGGTA | 10533 |
| rs545895256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336306 | CCCAAGGTGCTAGGA[C/T]TACAGGCGTGAGTCA | 10533 |
| rs545895336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343270 | TTCCAAAAATGTTAC[A/T]CATATGAGACACAGA | 10533 |
| rs545923882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549177 | TCCTGTCACCACAGA[G/T]GGGTTTTTGCCCTTG | 10533 |
| rs545932015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336775 | CCTCCCAGGCTCAAA[C/T]CATCCCCCCAGCTTA | 10533 |
| rs545946734 | snp | C/T | 0.0013395 | 0.0258449 | intron-variant | ATG7 | GRCh38.p7 | 3:11332957 | AAATAAATAAAAATC[C/T]GGGCATGACAACAGG | 10533 |
| rs545950401 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11289286 | TAACTCTGTCTATGA[C/G]TCACTTCCCCCCAAA | 10533 |
| rs545969082 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ATG7 | GRCh38.p7 | 3:11452024 | GGGACTTGGGGGGTT[C/G]GGGGGTTGTGGGAGG | 10533 |
| rs545989412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446227 | AAAATGTTTAGACCA[C/T]ATCTGCACCAGAAAG | 10533 |
| rs546004790 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338271 | CTCCATCCATGTTCC[C/T]GCAAAAGACATGATC | 10533 |
| rs546012502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11368001 | TATCAAGCACCTTCA[A/G]TGCCCCCCTCATGCC | 10533 |
| rs546013267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399235 | TACATATAGTCCCAG[C/G]TACTCAGGAGGCTGA | 10533 |
| rs546026339 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376561 | AGTCACAGAATTCAG[C/G]ATGAGGCAAGCTCAG | 10533 |
| rs546032969 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11327240 | GCAAGACATCAAATA[C/T]AACATGCATCCTGTG | 10533 |
| rs546037596 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357913 | ACTTGGGAAGCTGAG[A/G]TGGGAGGATCCCTTG | 10533 |
| rs546046364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11489917 | TGGTCAATGTTGGAA[C/T]AGGTGTGGTGTGGTG | 10533 |
| rs546063853 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322517 | TTTTTTTAATATACA[A/G]ACTTTTTGTATATTT | 10533 |
| rs546065065 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426401 | TATTTGGCTAGCTCG[C/T]ATGTCACACTTTTTT | 10533 |
| rs546069463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324126 | AAACAAAGTTTTTCT[A/T]CAGTTACGTTGAGCT | 10533 |
| rs546077686 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11500851 | GGCCAAGATGTTCTC[A/G]ATCTCCTGACCTTGT | 10533 |
| rs546091660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494368 | TCAGCTCCTTGATAC[A/C]ATCTGGGTAGGCCTG | 10533 |
| rs546095728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538177 | TCAGAGAGAGCATGG[A/G]GGTTTTGTGGGGACT | 10533 |
| rs546101228 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11320136 | TTTTGCCTGGAACTC[C/T]CTTCTCTCTCTTTTC | 10533 |
| rs546105422 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11374601 | ACTAAAATAAACTGT[G/T]GTGCTTCAAGAAAGC | 10533 |
| rs546113773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420059 | TGACAGGTTCTTGTT[C/T]AAATTCTTTGTGATA | 10533 |
| rs546121862 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11458289 | GTTTTGTTTTGATGG[C/G]GTCTTGCTGTGTTGC | 10533 |
| rs546142836 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11519852 | AGGCGTGAGCCACCA[C/T]GCCCAGCCGAGAGGA | 10533 |
| rs546152688 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556397 | GGCCGCCAGCACCGC[C/T]GACCCCTCCCAGAGT | 10533 |
| rs546156323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11467082 | TGAGCTGACATCATG[C/T]CATTGCACTTCAGCC | 10533 |
| rs546165622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555885 | TGAGTCGAGCTGACC[A/C]TTACAACAGTAGGAT | 10533 |
| rs546170817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513745 | CAAAGTGGGAGCCCA[A/G]GCAGAGGAGGCGCTG | 10533 |
| rs546174388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552738 | ATCCCCTGCACAGCT[C/G]AGGCACTGCCAGCAG | 10533 |
| rs546179600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11513281 | GTGGATGAGACTGGG[C/T]GCCGTGGAGCAGGGG | 10533 |
| rs546181846 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11407407 | GTTGAGTGTCTGGCT[C/T]TTCCAGGCACACAGC | 10533 |
| rs546188506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393215 | ACAGTATTTCCAGCC[A/C]ACACATATATATATT | 10533 |
| rs546214811 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412932 | GAAGTTAATTCCTAA[A/G]TATTATATTCTTTTT | 10533 |
| rs546229146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386869 | GAGATGGAATATACA[G/T]CCAGAGCTGGTGAGG | 10533 |
| rs546249318 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557436 | CTCCCCTGGGAGCTT[G/T]TAACAAAGCAGACAG | 10533 |
| rs546249374 | snp | C/G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509807 | TGCCAGCACTCAAAT[C/G/T]TTCCCTGACTCAGTT | 10533 |
| rs546255819 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415057 | AAGCCTACTGCACAC[C/G]TAGGCTATATGGCAT | 10533 |
| rs546257406 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11339628 | GGCAAGCAAAGCTTT[A/C]ATTAACATGAGAAGG | 10533 |
| rs546259265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347390 | GCCTCTTGAAGAAAT[C/G]GTACAAAATGTTCTA | 10533 |
| rs546262778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428185 | TGTCAAATGATTGCA[C/T]GGGTGCAAAGATCTA | 10533 |
| rs546285133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375622 | TGGAGTGCAGTGGCA[C/T]GATCGCAGCTCACTG | 10533 |
| rs546290665 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436224 | ATAATCAAATAAGAT[A/G]CCCAACATCAATAGC | 10533 |
| rs546296106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340168 | TTGGACTGTGATCTG[C/T]TCACAGGTACAGAAG | 10533 |
| rs546308994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11484222 | AATACAGTAGAACCC[C/T]GTGTCTACCAAAAAC | 10533 |
| rs546314344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304355 | GCTGTCAAAATCACA[C/T]GTGGTGTGGTTGATG | 10533 |
| rs546332578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325751 | GCTAAAGGTTACACA[A/G]GAGCAAGTGATCCAG | 10533 |
| rs546351848 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11395299 | GGAAATCTAGAAAAA[-/AAG]AAATAATGGTTCTAT | 10533 |
| rs546351989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392592 | AACCCACACCCCAAG[G/T]CTGTCTCTGTAGCTT | 10533 |
| rs546354552 | in-del | -/ACTTAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11318613 | TCATGTAACTCTTCT[-/ACTTAAA]ACCCTTCTAAGGTTC | 10533 |
| rs546365049 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11373801 | GTAAGGTGCAACTTC[C/T]GCTCTTTAAATTTTA | 10533 |
| rs546397114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282396 | TTGTTCCCTGGTTGA[C/T]ACACTGAAGAAGAAA | 10533 |
| rs546398884 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420499 | CAATTTTTATTCAAA[G/T]ATGTTGTCAATTTTT | 10533 |
| rs546405965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539690 | AACTCCCCCCGTCTT[A/C]AGCTATATTCGTTTT | 10533 |
| rs546427294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492136 | GGTCATAGGACCCTC[C/T]GAGCCAGGTGTGGAA | 10533 |
| rs546430267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455056 | AGTACAGTTATTTAC[A/G]TATAAATTCTAATGA | 10533 |
| rs546433479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281701 | ATTGCTTGAACGTGG[A/G]AGGCAGAGGTTGCAG | 10533 |
| rs546454107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412480 | CTGTGAGGATTGTTT[C/G]TGCGCTCTCTATTCT | 10533 |
| rs546455325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11472113 | TGGAGGTTAGACTCT[C/T]ACACAGATTTAAGCA | 10533 |
| rs546470655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11288721 | CAAAAGATTTAGATC[C/T]ATGTGGACAGAAACT | 10533 |
| rs546495934 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11354518 | GCTGGGCGTGGTGGC[A/G]CACACCTGTACTCTC | 10533 |
| rs546497914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419205 | CTCTTTGAAAATACA[C/T]TAGCAATTGTTTTTA | 10533 |
| rs546499697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449496 | GATTGAGACTGAGAG[A/G]GTGAGAGAGAGTATG | 10533 |
| rs546507789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407746 | CTGAAGCCATGGCAT[A/G]AACTCTGTGTTGGCC | 10533 |
| rs546509486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508425 | CATCCTGGGCCACAT[A/G]CGTTAGACAAGCTTG | 10533 |
| rs546522451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380375 | CCCTCCTAGCCAGGA[C/T]CCTCATAGAGCAATT | 10533 |
| rs546529275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461147 | GTGGAAGCCATGGAT[A/C]TAGGGTGTCAGTGCT | 10533 |
| rs546539542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369793 | CTTACAGGTTGAAGG[A/G]TGTCACTTTGCCCCA | 10533 |
| rs546543273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474766 | ATGCAAAGAAAGGAG[C/T]CAGACATGTGAGGAG | 10533 |
| rs546544443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11546439 | GGCTTCCCAAAATGT[C/T]GGGATTACAGGCGTG | 10533 |
| rs546546131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11501879 | ATTTTTAGCAGAGAC[A/G]GGGTTTCACCATGTT | 10533 |
| rs546575752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503541 | AGGTGGGCAGATCAC[C/G]AAGTCAGGAGGTCAA | 10533 |
| rs546583060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, splice-acceptor-variant | ATG7 | GRCh38.p7 | 3:11510184 | CTTTACCCCCTTTCA[A/G]GATCATCTTTCTTTC | 10533 |
| rs546583203 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436861 | GTCCAGAGTTTTAAA[C/G]TCCATATAGTCAAGA | 10533 |
| rs546616944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482104 | TCTCTCCTGATGCCC[C/G]GGTTCCTTCTCTCAT | 10533 |
| rs546646230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290717 | GAGATAGAGTTTCAC[C/T]CTTGTCGCCCAGGCT | 10533 |
| rs546647508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427396 | GACCCTGAACCCCAC[C/T]ATGAAATGGCTTCCC | 10533 |
| rs546661715 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11368869 | CTTTAGGTGAATGAA[A/C]TCTTGGTTCTAAAGT | 10533 |
| rs546672009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306726 | AGCATCCTGATAGGT[C/T]AGAGTATAGGGAATA | 10533 |
| rs546675197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11348204 | GAGAGGGATAAAAAA[A/G]CACAACCAGGTCAGG | 10533 |
| rs546683064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290060 | TCTATAGTATAGACC[A/G]GGTAGGAAATAGATG | 10533 |
| rs546695228 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11282863 | CCTCCCGACTCCTGG[G/T]GATCTCTACCTCCTT | 10533 |
| rs546708847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299090 | AATCCAAATAATACC[C/G]ATTACTTAGCATTGC | 10533 |
| rs546715572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11395076 | GAAACTCTAAAATAC[A/G]GCTTTCCAGATTTAA | 10533 |
| rs546716110 | in-del | -/TC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325822 | AATTGTAACTCAGTG[-/TC]TCTGTAGGAACGGCA | 10533 |
| rs546716179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516400 | AAATGACTAGATACC[A/T]TGTAAACACCTACTA | 10533 |
| rs546726338 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11362033 | TCTCTTTTATGGAGA[A/C]AGATGGCTTGATGAT | 10533 |
| rs546753559 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11511620 | AGCCCTTGGGCGGTC[A/G]ATGGGACTGGGCGCC | 10533 |
| rs546754609 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270479 | AGCTTGAACTAGCAT[A/G]CTGTCTCATGTGTCC | 10533 |
| rs546755613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504909 | GGGAGGCAAGAGTTT[C/G]CCATGACAGGGGTAA | 10533 |
| rs546771700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401586 | TCAGCTTTTAACTTA[A/G]GGGTTTTTTAAATGT | 10533 |
| rs546777164 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11552985 | TTATGAACAGAACAA[-/C]CCCCAACCACCCATT | 10533 |
| rs546791212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277073 | CTTCCAAGTCCAGGT[A/G]GTCATCAGAGTTCTA | 10533 |
| rs546802140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307345 | GCTCATCTCCAGCCA[A/G]CATTTTGAAGCAGCC | 10533 |
| rs546809375 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410803 | ATTTTGTTTATCCAT[A/T]CATCCATGGATGGAC | 10533 |
| rs546809389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535597 | AGCCCTACAGGAGGA[C/T]TCAGCTCTTCAGCAG | 10533 |
| rs546812551 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11541107 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 10533 |
| rs546816892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285375 | GAGATGGGGGCCCAC[C/T]GTGTTGCCCAGGCTG | 10533 |
| rs546836640 | in-del | -/TT | 0.318754 | 0.24036 | intron-variant | ATG7 | GRCh38.p7 | 3:11390673 | TGTGGGTGGGTTTGA[-/TT]TTTTTTTTTTTCCAG | 10533 |
| rs546838216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11540431 | ATCTTATTGAACTGT[A/T]AGAGTTCTTCCACCC | 10533 |
| rs546847953 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384807 | CTCTACAAAGAATAC[A/G]AAAATTGGCCAGGTG | 10533 |
| rs546849831 | in-del | -/ATTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462897 | TTTATTTATTTATTT[-/ATTT]TTGAGACAGAGTTTT | 10533 |
| rs546852763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334535 | AGGCATGAGTCACTG[A/G]GCCTGGCCTCATATA | 10533 |
| rs546853339 | snp | A/C/T | 0.00103586 | 0.0227348 | intron-variant | ATG7 | GRCh38.p7 | 3:11362779 | TTGAATGGAGTAGAA[A/C/T]GTTCTGCACACACCA | 10533 |
| rs546867907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511360 | AGTTAGATACAGAGT[G/T]TCGACACACAGGTTC | 10533 |
| rs546868635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284324 | CTGCTTCAATTAATT[C/G]TATAAGCAGCCAAGC | 10533 |
| rs546870475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421396 | GTTGTCATTTCAACA[A/G]TGTTCACAGCATCTT | 10533 |
| rs546874725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414153 | CTGTAACCTCCACCT[C/T]CTCCCAGGTTCAAGT | 10533 |
| rs546878185 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11482750 | ATCTAGTGCCAGGCT[A/G]CTAATCCAGTGCTTT | 10533 |
| rs546884294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389930 | TTTTGTGTTATGTGC[A/G]AAGGCCTGGGAAAAA | 10533 |
| rs546888122 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11449163 | TGTAATGCAGAGGCC[A/G]CTGTCTCTGCCTTCA | 10533 |
| rs546903397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504111 | ACACTAAGGTTCATC[A/G]TAGTGAATTTCAAAA | 10533 |
| rs546914208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454436 | AATTTGACGGCATGA[A/G]TCTGGGCTGGGGCAG | 10533 |
| rs546921468 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429229 | GGCGGGGCGTGGTGG[C/T]TCACAGCTGTAATCC | 10533 |
| rs546922476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11376268 | GTGATGATGGTTGCA[A/G]AACTGTTCATATACT | 10533 |
| rs546925433 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11292551 | AGGCGTGAGCCACCA[C/T]ACCCAGCCTCCTTGT | 10533 |
| rs546932571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308084 | AGCAGCTTCTGCCCC[A/G]TGCCCCCTCGGCTTA | 10533 |
| rs546947652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392228 | ACAAACATAGTTCAT[A/C]TCCCATTTTGGTTAA | 10533 |
| rs546947913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398997 | GTAAAATTGCTAAAC[C/G]TATGGTGAGGCTGAG | 10533 |
| rs546951426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429748 | AGCTCAGGAGTTTGA[A/G]ACCAGCCTGGGCAAC | 10533 |
| rs546969718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475754 | CTGCTAGGTCAGTTT[C/T]AAGCTAAAATGATCT | 10533 |
| rs546974359 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293165 | AAGGACACTTAAATA[C/T]ATGTTTAGAGGTTAG | 10533 |
| rs547001793 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286584 | TTCTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 10533 |
| rs547005457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348690 | GAAGGGGACCCAAGT[A/G]GGTTGCTGCTGCTGG | 10533 |
| rs547012622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383413 | ATGCTGTCTCCTCAT[A/G]TCAGGAGTTATATAA | 10533 |
| rs547014125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443825 | ATTTTAATATTTCCA[A/T]ATGAGCTATAACATA | 10533 |
| rs547028538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437272 | CCATTTTTATTGTGC[C/T]TCAGTTTTCAAAGCC | 10533 |
| rs547038533 | snp | C/T | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557387 | AAAGGGAGCAGTTTC[C/T]GCATGTAGGGAAGTT | 10533 |
| rs547042257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11489265 | CTGCTGTCTTTTTGC[A/G]TAGAGGTGTTTGTAG | 10533 |
| rs547042311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494640 | TCACTTTAAGCTGTT[G/T]AGCAGAGCAGAATAG | 10533 |
| rs547068544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539652 | TTTTTGGTAATTATT[A/G]TAAATATGTTTTTAT | 10533 |
| rs547076517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11402279 | TCTACTAGAAATACA[A/G]AAATTAGCTGGGGTG | 10533 |
| rs547080797 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11357884 | TGTGGTGACGTGTGC[C/G]TGTAGTCCCAGCTAC | 10533 |
| rs547084522 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353214 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACGAGG | 10533 |
| rs547084564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522293 | TCATGTTGATGGAGT[A/G]TCAGGGAACTCTGAC | 10533 |
| rs547104212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11490094 | TTAAAGTCTCCCATT[A/G]TTATTGTGTGGGAGT | 10533 |
| rs547107198 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11449960 | GTTTTGTGTTTGGCC[A/C]TCAATAAACTAGTCT | 10533 |
| rs547108885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352214 | GCATAGTATTCCATG[A/G]TGTATATGTGCCACA | 10533 |
| rs547134086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529657 | CAGCCTTAAAAATAG[A/G]GAACTTCTTGATTTT | 10533 |
| rs547134094 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386897 | AGGAGTATTTAGCTA[C/T]AAGCCTTAACCTCAG | 10533 |
| rs547139838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469077 | TGAATCAAGTCCTGA[C/T]CTGTCAACAGAAGAT | 10533 |
| rs547140162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383902 | TAAAATTTATATATG[A/G]TGAAATGTATGAATC | 10533 |
| rs547143904 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11466681 | AAAAGCAGTTCTCAG[A/G]GGGTTGTATGAAGGA | 10533 |
| rs547150951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513389 | CTGAGCCCTGCCCCG[C/T]GGGGAGGCAGCTAAG | 10533 |
| rs547151270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508080 | CTCATCTCTATGGAA[C/T]TAAAACAAAAGTGTT | 10533 |
| rs547151321 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312845 | GTATCTATGGTCAGT[A/G]GAAAAAAGCTTAAGT | 10533 |
| rs547156472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430255 | AAAAATTACTGTTCT[A/G]ACTACATCATTTTCT | 10533 |
| rs547179979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11288956 | ACTAGAGTTCTTGCT[C/T]ATTACAGTGTTGAAT | 10533 |
| rs547200656 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475590 | AAAACAGACGCGGAT[A/G]CTACCCTCTGCAGTC | 10533 |
| rs547201171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452195 | TTCAAGACCAGCCTG[A/G]CCAACACAGTGAAAC | 10533 |
| rs547208635 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498650 | TGGCCAGACTGGTGA[A/G]GCCAGGTGTCCTCAC | 10533 |
| rs547217202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423102 | AATGTGTGACTCTTC[A/C]TTTCACTTGGACACT | 10533 |
| rs547239040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508738 | TTACAGGTGTCAGCT[A/G]CCATGCACAGCCCTA | 10533 |
| rs547250129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386994 | CATACAGTGGGGAAA[A/G]TATTTTCTGTTTCCC | 10533 |
| rs547254476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11452177 | TTACCCTGAGGTCAG[A/G]CATTCAAGACCAGCC | 10533 |
| rs547264223 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523037 | GCCGATGAAATAGCC[C/T]GTACTTTATAAAGTA | 10533 |
| rs547287400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437893 | TCACAGAACAACAAA[G/T]AATAATTCCATAATA | 10533 |
| rs547312468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512963 | AGATTAGCTAGATAC[A/G]GAGTGTGGACACAAA | 10533 |
| rs547312636 | in-del | -/CTCCGTGTCCCGAGCAGCCCTGCCAGGCCTAGCT | 0.0341408 | 0.126114 | intron-variant | ATG7 | GRCh38.p7 | 3:11545659 | GGGGCTGTGCTTGGG[lengthTooLong]CTCCTGGGCGTGTGT | 10533 |
| rs547315386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426095 | TTGTTTGTGTCTTCT[C/G]GTGCACATATGTACA | 10533 |
| rs547321186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468403 | CTCGCCTATCCTCCT[A/C]CCCACTCCATGTCCC | 10533 |
| rs547321282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335372 | TACACTAACACTAAT[G/T]ATAGCTGATGAGCTA | 10533 |
| rs547323179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341998 | TCCTCCCTGCTTACC[C/T]TCCAGTTTAATTTTC | 10533 |
| rs547330917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303856 | GAGGCGGGTGGGTCA[C/T]GAGGTCAGGGATCGA | 10533 |
| rs547356088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547335 | CGGGAAGAGAGTGGA[G/T]GCAGGGGTTTGAGTG | 10533 |
| rs547364392 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11554001 | CTCCAGGGAGCCCTG[C/G]GTGCCAGGGGCCCTG | 10533 |
| rs547364466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492271 | TAGGCAAGGGAACTC[C/T]CTGACCCCTTGCACT | 10533 |
| rs547365459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525786 | GTCTCGATCTCCTGA[C/T]GTTGTGATCTGCCCG | 10533 |
| rs547371665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304590 | CAGAGGATTTATTCC[A/G]TTCTGACCACCTGCC | 10533 |
| rs547380247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479460 | CCAGCACAAAATCCA[A/G]ACATCGTAAAGTTAC | 10533 |
| rs547381048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533897 | CTTTCCTATTTTGCT[C/T]TTAAAAATTTAAGCA | 10533 |
| rs547397095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520238 | ACCCCAGCTCATGCT[C/T]CACACCTCGATATGC | 10533 |
| rs547399956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11484366 | GCCACTGTACTCTAG[C/T]CCGGATGACAGGAGA | 10533 |
| rs547404161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11519707 | TGGGACCACAGGCGC[C/T]CGTCACCGCGCCCGG | 10533 |
| rs547410706 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11351571 | GAGAGAGCAAGTCCA[A/G]CTGTTCTTGGAAACA | 10533 |
| rs547414750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439723 | TAGGTTTTGAGGTGC[A/G]TCTTGAAGGTTGGAG | 10533 |
| rs547415050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446297 | ACATTCTGTGATAAC[A/G]ATAGAATAAGTCTTT | 10533 |
| rs547417128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440267 | CGACTCCAATCCCAA[C/G]TTACCATTGGGAAAA | 10533 |
| rs547417672 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404271 | CTCCCGAGTAGCTGG[G/T]ATTACAGGTGCTCGC | 10533 |
| rs547426690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11358701 | CCCTTCCCCAGGGCA[A/G]AGATGTGGTTTGTGT | 10533 |
| rs547447349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344072 | TGTTTTTTCCTTTAG[A/T]GATATTTTCTCCCGT | 10533 |
| rs547448851 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386131 | CCTTGCTGGACTGCC[A/G]AGTGACCACAAGCAA | 10533 |
| rs547449043 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11502743 | CCCATAGAGCCTCCT[A/G]AAGACTTGGATTTGG | 10533 |
| rs547458036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325463 | GATCACCTGAGGTCC[A/G]GAGTTCGTGACCAGC | 10533 |
| rs547460646 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11404196 | GGAGTGCAGTGGTGC[A/G]ATCTTCTCGGCTCAC | 10533 |
| rs547465978 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430377 | AGTAGTGTTTTGATT[A/T]ACATACTTGATTCTC | 10533 |
| rs547482250 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11379527 | GCCTTCCACAGTCCC[C/T]CAAGCCATCTTTCCT | 10533 |
| rs547482621 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11483268 | CATCACAGAAGCTTG[A/T]CGAGAAGAGAAACAG | 10533 |
| rs547484367 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555371 | AGGAGGAGAGCCGAG[C/G]TGGGTACGAGACTAA | 10533 |
| rs547492509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274957 | TAAATTACCCAGGCA[A/G]CAATGTGGTGATTAC | 10533 |
| rs547500575 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376733 | TCTGCCTTATTTATT[A/G]TTTATATTTTATTTT | 10533 |
| rs547501802 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11552693 | AAAATAATAATCCCC[A/G]CACAATAAGTCTTCT | 10533 |
| rs547502290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317117 | AGTGCTGAGATTACA[C/G]GCGTGAGCCACCACT | 10533 |
| rs547527725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281850 | ATCAGGCCTTTGCTT[G/T]GCCCAGTTTTAAAGT | 10533 |
| rs547540812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317736 | CAGCTGGGACTACAG[A/G]TGCGCACCATCATGC | 10533 |
| rs547548629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11425372 | TTAAAGGGTGCCTGC[A/G]TTTTCATCTTCTGAA | 10533 |
| rs547551314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445746 | TTCCAAAGCAGTTCA[A/C]TGACTTACATGAATA | 10533 |
| rs547561157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281203 | TATGCAGGCTGTGCA[C/G]TGCACAAGAGGCCAC | 10533 |
| rs547576184 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11400635 | AAATACTGCTTGAGT[C/G]AAACCAAACCTGTAC | 10533 |
| rs547579035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544993 | GGGCTGAGAATAAGG[C/T]AGGCCAGCAGGGAAG | 10533 |
| rs547582935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326157 | ACACATACCTGCTTA[A/C]TGTTAAGCAAGTGAG | 10533 |
| rs547584177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441839 | ACCTGGCTAATTTTC[A/G]TATTTTTAGTAGACA | 10533 |
| rs547585275 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11408709 | CGCCTCGTTAAAACT[A/G]CCATATCTTGTGTGA | 10533 |
| rs547588693 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11545411 | TCTCTTGTGGGCATC[G/T]AGAGCCTGCGCAGTG | 10533 |
| rs547596476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442253 | TGGAAGGGAGCATAG[A/G]ATGTGGGTCCTGAAG | 10533 |
| rs547608800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345133 | TTGTTGGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 10533 |
| rs547608900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337781 | GGACTACAGACATGA[A/G]CCCAGCATCTGTAAC | 10533 |
| rs547633383 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11549781 | TGGATCACATGGTGA[C/G]CGCACACTTAAACAG | 10533 |
| rs547668959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353425 | CTCCAGCCTGGCGAC[A/G]GAGTGAGACTCTGTC | 10533 |
| rs547669318 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11311559 | GTGAGCTGAGATCGT[C/T]GTGCCGTTGCACTCC | 10533 |
| rs547673419 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555564 | GGAAGAGCCCAGGGG[C/T]AGATCCTGGCAGCTG | 10533 |
| rs547689405 | in-del | -/TTAA | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11301959 | GTGAGCATCTTAAAC[-/TTAA]TTAATCTAAAAATTT | 10533 |
| rs547714823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521696 | TAGCTGGGATTACAG[A/G]CGCCTGCCACCACGC | 10533 |
| rs547715181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471523 | CATTTTGCAGATGAA[A/G]ATAAGAAACTTTAAA | 10533 |
| rs547723206 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280210 | TGCCACCATGCCCGG[C/T]CCTTTTTTTGTATTT | 10533 |
| rs547727522 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366398 | ACACACAAGGTGGCA[-/T]TTTTTTTTTGACATG | 10533 |
| rs547743129 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11385662 | ATTAATTTTGTAAAT[A/G]TGGAGGACTAGGGAA | 10533 |
| rs547745845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538406 | CATGGGACGAGACAG[A/T]CCTATGTGTGGATCT | 10533 |
| rs547760108 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503551 | ATCACGAAGTCAGGA[A/G]GTCAAGACCAGCCTG | 10533 |
| rs547760157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11556021 | CACAGGTGCAGGGCC[C/T]GAGTCCGCCCACCCA | 10533 |
| rs547764925 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11542080 | AGCGGAGAGGCTGGA[A/G]CACTGGACAGCATAC | 10533 |
| rs547766836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536266 | TCTTTAAGAACTGCA[C/G]TTACTGAATACAGCC | 10533 |
| rs547790654 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429032 | GCCTGAGTTTTCTTT[C/T]TGAATTTTCCTCTAC | 10533 |
| rs547796311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450236 | AAGTGTTAGAGCCAA[A/G]TCGTTTGGCTCCAGA | 10533 |
| rs547801636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405899 | GCTAGGATTATAGGC[A/C]TGATGCCTGTAATCC | 10533 |
| rs547808816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11416346 | GGCCTGGTGCTTTCT[A/G]TTTGGGAAGGTTATT | 10533 |
| rs547829107 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11310655 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 10533 |
| rs547831003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322115 | CACTTCTTGGGTGAT[A/G]TATGGTTGTTACTGT | 10533 |
| rs547835463 | snp | A/C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11453985 | CATCAGAGGAAATTC[A/C/T]GTGTAAATAAATGTG | 10533 |
| rs547835608 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11544361 | TAACCCGTGAGGCCC[A/C]CCATCTGCAGAGCCC | 10533 |
| rs547836644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422363 | AGTACTTGCTGCTTC[A/G]CCTCTCACTTTTATG | 10533 |
| rs547847210 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11344086 | GAGATATTTTCTCCC[A/G]TTAAACTTTCCAGTT | 10533 |
| rs547850170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490911 | CCCTTAACATTTTTT[C/T]CTTCATTTCAACTTT | 10533 |
| rs547850902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328495 | TTTGCGTTTAAGAAA[C/T]GAACATGCATTTAGA | 10533 |
| rs547876139 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11427793 | GCACTCCAGTCCGGG[C/T]GACGGTGCGAGACTC | 10533 |
| rs547877207 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11421598 | CCTCAAAGTCATCCA[G/T]GAGGGTTGGAATCAA | 10533 |
| rs547889328 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11329015 | ACTAGAATTGCTTGA[A/T]TCCTATGAGGTGGAG | 10533 |
| rs547904330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408483 | CTTTTCAGCAACACC[C/G]CATTCCTGGTACCAG | 10533 |
| rs547921457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11521214 | CCATAGGCAGCCATG[A/G]GTTGAGAAGGCCAGT | 10533 |
| rs547923272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345286 | TGGTGGCAGGCGCCT[G/T]TGGTCCCAGCTACTC | 10533 |
| rs547925449 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11509273 | CTGCTGCCGGCAGGA[-/G]GGGAGCCGAGCTGTT | 10533 |
| rs547930933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277304 | TTTTCACATAAGGCT[C/G]TTCATGATATGGCCT | 10533 |
| rs547937061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400851 | CACTCAGGGTAATAA[A/T]TTTCTTAGTGAAACC | 10533 |
| rs547946320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547207 | GGAAAAGGCCTCTTC[C/T]TTCGCCCTTGCTAGC | 10533 |
| rs547969388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444373 | CAGTTTAGAATTTAA[C/T]TAATACTAAAGAATA | 10533 |
| rs547969679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394435 | TGAGTTGAGCTTTGA[G/T]AGAGAATGTAAGCAC | 10533 |
| rs547982839 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ATG7 | GRCh38.p7 | 3:11444876 | TTACAAGGAAAAAAC[C/T]CCATTAAAAAGTGGG | 10533 |
| rs547996680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480210 | TGCTGGGATTACAGG[A/C]ATGAGCCACCGCACC | 10533 |
| rs547998294 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11415740 | TGATAGCAATGCCTT[C/T]TTCTGGAATGCAGTT | 10533 |
| rs547998495 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339268 | GCCACTGCACTCCAG[C/T]CTGGGCGACAGAGCG | 10533 |
| rs547999451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349606 | GAAAGGAATGTATGA[A/G]TAAATGTTTTGTAAG | 10533 |
| rs548006490 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501720 | TTTTAGACAGAGTCT[C/G]CCTCTGTTGCCCAGG | 10533 |
| rs548018858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461927 | CCCAGCTACTCAGGA[G/T]GCTGAGGCAGGAGAA | 10533 |
| rs548019260 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349568 | AATAATAAATAATCC[A/G]TCTCACATATTCTTG | 10533 |
| rs548036528 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485610 | TTTAGACATGAAGTT[C/G]TTGCACATGCCTATG | 10533 |
| rs548047074 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282377 | AGACTGTGGATGTGA[C/T]TGCTTGTTCCCTGGT | 10533 |
| rs548050433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11514372 | TTTCTTGGGATGCCC[A/G]TCTGACCTTCCCTTT | 10533 |
| rs548062857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491304 | CACGTAGTTCTCAAG[C/T]CTTGGCTTTCAGCTC | 10533 |
| rs548069346 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557008 | AACTGTAAAACCGGG[A/G]GTCATACGGTGTGCA | 10533 |
| rs548085956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11527565 | TACATAAACACCTCA[A/G]TTATCAGTATTATCA | 10533 |
| rs548119107 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345302 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10533 |
| rs548123058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485253 | AACTGGTGTGAGATA[C/T]CTCATTGTGGTTTTG | 10533 |
| rs548129816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462777 | GAAAGGTTTTTTAAA[A/G]GATGTTCAAACATCG | 10533 |
| rs548140166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505264 | AGGAGTTCTATAGGC[C/T]TAGGGAATGGAGGAG | 10533 |
| rs548142738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469916 | AATCTCTTGAACCTG[A/G]GAGGCGGAGGTTGCA | 10533 |
| rs548160231 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554954 | GGGCCCCTCCTCCAT[A/C]CCCCGAGGTCTGGGA | 10533 |
| rs548164857 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341924 | GGAACTCAGTATCAA[A/G]TCTGTGGCCCCCTCG | 10533 |
| rs548172263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342824 | TACTTGTATGTTTAT[A/T]TATCCATAGGATTTT | 10533 |
| rs548175076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371075 | GGCCAAAATGAGATG[C/G]AATGTATGAAAACAC | 10533 |
| rs548177706 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11333902 | ACAGGCGCCCACTAC[C/T]ACGCCCGGATAATTT | 10533 |
| rs548181955 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11503814 | TTAGAAATTAAATAT[A/G]TAAGTTTAAAATTCA | 10533 |
| rs548185841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277631 | GGTCACAAAGATCAC[A/G]TGCTTCTGAGGAAAC | 10533 |
| rs548188445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378592 | CGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 10533 |
| rs548191185 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271350 | CTCAGCCTCCCAAGT[A/G]GCTGGGACTACAGGC | 10533 |
| rs548195743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11530495 | TTGCTTTAAAGAAAT[A/G]CAAGAAATGCAAAGA | 10533 |
| rs548204467 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11439559 | GTCAAAGAGGTACAA[C/G]CCAGGCTTTTAGGAG | 10533 |
| rs548231642 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11350541 | GGAACAGTCATGTGG[A/G]TCCTACTCTTCCTAT | 10533 |
| rs548238503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335286 | CACTTAAAGATAGTC[A/G]CAGGGGTGTCCAATC | 10533 |
| rs548249572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492412 | GATGGAAATGCAGAA[A/G]TCACCCGTCTTCTGT | 10533 |
| rs548285057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335982 | GATTACAGATCCACC[C/T]GCCTCGGCCTCCCAA | 10533 |
| rs548292107 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532192 | AAGCGTGTATTGAGT[A/G]TGATTTCTGATTTGT | 10533 |
| rs548321460 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11286282 | CTTGACTACTTTCAT[A/T]TGCAGTTGCATAAGG | 10533 |
| rs548323679 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376333 | TTTTATGGTATGTGA[A/G]TTATATCTCAAACCC | 10533 |
| rs548345407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357102 | GCTGTGTCCCTTGAG[A/C]TATTTTTCCAGTAGG | 10533 |
| rs548352255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273058 | ATGATGTTGGAGAAG[C/T]ACAAGCCAAACCGTG | 10533 |
| rs548352848 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11286402 | ATATGGCATATCGTC[A/G]TATGTTCTTCATGAT | 10533 |
| rs548357314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430397 | ACTTGATTCTCAATG[C/T]GTTTACAGGTGGTCA | 10533 |
| rs548362191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530917 | CCCTGGGAGGCAGAG[G/T]TTGCAGTGAGCCAAG | 10533 |
| rs548374226 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315719 | ATAATTTTGATACCT[C/T]ACTCTTTTTTTTTGT | 10533 |
| rs548390347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390778 | TTAAAGTACTGCAAG[G/T]CTTAAAATGGCACAT | 10533 |
| rs548391471 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456608 | TTAACACTAATACAC[C/G]TTGCCTCCCCTAGGA | 10533 |
| rs548436229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488629 | GGGCCTTCGAGCCTT[C/T]TGGGGCCTCCGGCGC | 10533 |
| rs548449703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470516 | GAAACGTCATTATGT[A/G]GTGTGTCACTGCTTA | 10533 |
| rs548458953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492908 | CTCCAAGGCCCCAGA[A/G]GGCATGTTACAATGC | 10533 |
| rs548466925 | in-del | -/AACACACACA/ACACACA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478988 | TGCCTGTATATTTAC[-/AACACACACA/ACACACA]AACACACACACACAC | 10533 |
| rs548483402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315636 | CATTTCCTTATCTCT[A/G]TCCTCTCCCACCCCT | 10533 |
| rs548506375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402964 | TCAATGCTTTTAAAG[C/T]CTTAATTAAAACCAG | 10533 |
| rs548509801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464586 | TCATTCTTGTTTCTT[A/G]CCAAACCTGGGAATG | 10533 |
| rs548510492 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363553 | CATTGCACCCGGCCT[C/T]CTTTAATCTTCATAG | 10533 |
| rs548516162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372037 | TTGCATGCTGTCTGC[C/T]GTGTTTTCATTCCCC | 10533 |
| rs548522512 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11488428 | CATCCTCCCGGCGGT[C/T]GGGCAGCGGCGGCTG | 10533 |
| rs548537176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384685 | GCATGAAAGGCTAGG[A/C]ATGGTGGCTCACACC | 10533 |
| rs548539723 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322065 | GTCTTTAAATGAAAG[A/C]TCAAAAGCAAATGCG | 10533 |
| rs548542175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473310 | TACCCAGGAAGAAAA[C/T]TGTCACTTACTGAGT | 10533 |
| rs548548700 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271867 | GCTGTATCTTCAACA[A/C]CTGTCCAGTGCTTTG | 10533 |
| rs548555572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286863 | TCCCGCCTCAGACCC[C/T]CAAAGTGCTGGGATT | 10533 |
| rs548566291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11346127 | CTTGTGATGTTCCCA[A/C]CTTGGCCTCCCGAGT | 10533 |
| rs548569016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542769 | TCTCTGTTTCCAGCC[C/T]GGGCTCTGTTCTTGG | 10533 |
| rs548572899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11294837 | AAGTGCTCAAAGGCC[A/G]GGAGCAGTGGCTCAC | 10533 |
| rs548587340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500125 | CTTTTAATTCCCTTC[C/T]AGGGCTAATGCTCTT | 10533 |
| rs548587861 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557312 | AGCGTACGAGGAAGC[A/G]TATAAAACACCATAT | 10533 |
| rs548594181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393547 | ATGTCTTGTATAATG[C/T]TGCCAGCCATTCATG | 10533 |
| rs548603669 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535174 | TTCGGGGCCTGGACC[C/T]GGGCCATGCCCTGCT | 10533 |
| rs548607961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330490 | GCCTGTATCACCTTG[A/G]CATGCCCCAATTCAT | 10533 |
| rs548628222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345338 | GGCGTGAACCCAGGA[C/G]GTGGAGCTTGCAGTG | 10533 |
| rs548629402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438658 | GTTATCTGACCTGGC[C/T]AGAAGCTCTGATTGG | 10533 |
| rs548637474 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430774 | ATGTTTTAGTCATTT[G/T]TATATTAAGTGCTGA | 10533 |
| rs548644474 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11423813 | AGTGGTGCTCACCAG[C/G]CCCTCAGTTTCTCTG | 10533 |
| rs548652269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511957 | CGCCGCATGCAGCCC[C/T]GGTTCCCGCTCGTGC | 10533 |
| rs548655623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483227 | AGAGGTAAAGTGATA[C/T]CCCCATCCTCTCTGG | 10533 |
| rs548663906 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11477400 | TAAATGGATAGAAGT[A/G]TATTTATATAATTCT | 10533 |
| rs548665699 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404697 | GGTTTAATGGACTTA[A/C]AGTTCCACATGGCTG | 10533 |
| rs548682375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11434200 | TGTGGAATATTTTTG[C/T]TTTGTTTTGTTTTGC | 10533 |
| rs548696826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289950 | GGAACCCCTTTGGTC[A/G]CACATCTTCCCAGTC | 10533 |
| rs548699528 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11397625 | TCTTGCCTGGCTAAT[A/T]TTTGTATTTTTAGTA | 10533 |
| rs548712910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457879 | GCAAGGACTGTGTCT[C/T]AGATAATATACCCTC | 10533 |
| rs548719000 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331107 | TTTCTGCCAGGCACA[A/G]TGCAAGGCACAGGGG | 10533 |
| rs548719401 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11319155 | ATTAAAGAAGGCTTT[C/T]GCCGGGGGCAGGGCC | 10533 |
| rs548732582 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11375555 | ACACTTTGCTAGTGA[C/G]ATTTTTTTTTCCCCT | 10533 |
| rs548733426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302994 | AAACACTAAGAAGTT[C/G]ATTTCTTGCTCATCA | 10533 |
| rs548735903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500594 | AAAGTTCTACACGTA[A/T]AATTTTTGAGTATAG | 10533 |
| rs548738971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339564 | AGATGTAGGGAGCGC[A/G]AGAGAGTGGGATCCA | 10533 |
| rs548752394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276376 | GTTCCATCATTTGTT[C/G]ATTTTCTTTTCTGTT | 10533 |
| rs548767601 | in-del | -/AAAAAAAAAAA | 0.368938 | 0.219895 | intron-variant | ATG7 | GRCh38.p7 | 3:11411620 | CAAGACTCTGTCTCC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 10533 |
| rs548769354 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441965 | GCCACCGCGCCTGGC[C/T]CAATTTTTGTATTTT | 10533 |
| rs548771313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441652 | TCTTCCTTCCCCTTT[C/G]TCCTTTTTTTTTTTT | 10533 |
| rs548779129 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11485175 | CCAGTGTAAAAGTGT[G/T]CCTATTTCTCCACAT | 10533 |
| rs548789202 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11451845 | TCTCTCTATCTCTCT[A/C]TCTATATATATATAC | 10533 |
| rs548818386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394369 | TAAGAAACTGGATCA[A/G]TTGCTTCTAAAAATC | 10533 |
| rs548824837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304589 | CCAGAGGATTTATTC[C/T]GTTCTGACCACCTGC | 10533 |
| rs548829742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532084 | CTCCCCTCCGCCCCA[C/T]ACGCCACCCTGTAAG | 10533 |
| rs548832506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330203 | CACTGTAAAAATACT[A/G]TTTTTTCTTTGAAAG | 10533 |
| rs548834196 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11549308 | TCACATAGTGAAATG[C/G]TTACTACAGTCAAGG | 10533 |
| rs548845943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324436 | CAGCTTAGTGTTAAA[C/T]GGATTTTGTCATTTT | 10533 |
| rs548848651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507020 | GCGCAGTGGCTCATG[A/C]CTGTAATCCCAGCAC | 10533 |
| rs548850034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316609 | CTTTTTGTGCCATAT[C/T]AGACTGTAAGCTCCA | 10533 |
| rs548851562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474003 | ATACATCTGATTTGG[C/T]AAGACAGTGGCCAGG | 10533 |
| rs548854552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287478 | ATCAAGTCAGAGGTG[A/G]GGAGTGACAGGGCCG | 10533 |
| rs548856308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417299 | GCTACAAAAGTAGAT[C/T]CGTCTATTTCTTCTT | 10533 |
| rs548868971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543260 | CCTTAACCTTGTTCC[C/T]GGAACCCCGGAGCAG | 10533 |
| rs548875862 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11503496 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10533 |
| rs548882685 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363531 | TGTTGGGATTACAGG[C/T]GTGAGCCATTGCACC | 10533 |
| rs548893223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374708 | CAGGAGATTGAGACC[A/G]TCCTGGTTAACATGG | 10533 |
| rs548917382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11417912 | GCCTTCTGGGTTCAC[A/G]CCATTCTGCCTCAGC | 10533 |
| rs548948446 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356876 | CTGTGCTAGTCTCAT[C/T]ATTAAAATAGATGTG | 10533 |
| rs548957807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514344 | ACTTTGAAGATGGGC[A/G]TTTGCAATTCATTTT | 10533 |
| rs548960135 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11507847 | AAGGACTGGACCTGG[C/T]AGTTGCTCACATCCC | 10533 |
| rs548961187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338834 | TGGTTTCTCATTGAC[C/T]GTCCTATCCCAGAAA | 10533 |
| rs548980238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333228 | CCTCTTTGCCAATGC[A/G]GACACCTACTTCGAA | 10533 |
| rs548990477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11510097 | TCTTCTGCCCCTCCC[C/G]CAGCCAGCTGGTGTC | 10533 |
| rs548996402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546754 | TTGTGATGGGCCCAA[C/T]TGAAAGGTCCCTCTT | 10533 |
| rs549003314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522251 | AGCCCTGTGGAAGAG[A/G]TAAGTCACCACGCAG | 10533 |
| rs549016019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469493 | CCACCAACAAACCTA[C/T]CTATTAGTCCACTGA | 10533 |
| rs549021912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11497712 | ATGTTGTTTGTGAGC[C/T]GTTGTTGAAGGGCAA | 10533 |
| rs549030646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11433111 | AGCCTGGGCTAGATG[A/G]TGAGCCTCTGTCTCT | 10533 |
| rs549063525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306794 | TTCTTGAGTTATGAT[A/G]TTCATCTTTTTCCAA | 10533 |
| rs549083493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11492111 | GTGCTAGCAATCAGT[A/G]AGACTCCGTGGTCAT | 10533 |
| rs549099090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400233 | AACCTTAGGCTGTAA[A/G]AGACTGAGTCCAATG | 10533 |
| rs549104098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529109 | GAAACTACACGTGTA[C/G]GTGGACAGGAGGGCA | 10533 |
| rs549112145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11443087 | CTTCCCTGTTTTGAA[A/G]TTGACTCCTCAAAAG | 10533 |
| rs549128119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11516302 | GTAACAAACCTGCAC[A/G]TTGTGCACATGTACC | 10533 |
| rs549135459 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429074 | TTTAGTTTTGGAATC[A/G]TACGTCACATCAAAT | 10533 |
| rs549137137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486055 | CATATGAACTTTTAA[A/G]TAGTTTTTTCCAATT | 10533 |
| rs549140726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428894 | GTTTCTAGATTTAAC[C/G]TGGTTTATCTTACAT | 10533 |
| rs549157210 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11398218 | TGAATACATATAGAA[A/T]ACTGCACCTAACTGA | 10533 |
| rs549200133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407263 | ATCTCCTTTGACTCC[A/G]TGTCTCACATCCAGG | 10533 |
| rs549214034 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11511289 | GTCAGGGCGCTGATT[G/T]GTGCGTTTACAATCC | 10533 |
| rs549223562 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11454364 | TGGGCACATGACCCA[A/G]TCTTAACCAATGAGG | 10533 |
| rs549229057 | snp | A/G | 1.65048e-05 | 0.00287265 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11313329 | AGTACCACTTCTACT[A/G]TTGGTTTTGCTATCC | 10533 |
| rs549244097 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11319520 | TCTCTTCTGGGTTAT[C/G]TCATTGTGCCTACAA | 10533 |
| rs549248255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327626 | CACATTAGAATCACC[C/T]GAGGATCTTTTAAAA | 10533 |
| rs549254275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428011 | GAAATGTAGCTTATG[G/T]TGTGTTTCCACAAAC | 10533 |
| rs549272233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333648 | TGTGTGTGTGTGTAT[A/G]TATATATACACATAT | 10533 |
| rs549284152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382898 | TAACATTTTGCCCCA[C/T]GTATATTTGCTGTCG | 10533 |
| rs549289739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515822 | AAGACAATGAATTCT[C/T]TTGCTGGGCTAAAGA | 10533 |
| rs549292499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11553407 | GGGAGAGTGAAAGAA[C/T]GGATGGATTGTGCTG | 10533 |
| rs549304276 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11284552 | TTTGTTCTACTTTTT[A/T]ATTTTATTTTATTTT | 10533 |
| rs549306593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340833 | GTGTAATTCAGCCCA[C/G]GGGGTGCCAGTCATG | 10533 |
| rs549311612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420898 | GTAGCTGGGACTACA[C/G]GTGTATGCCACCTTG | 10533 |
| rs549320373 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11309501 | GTTTTCTGTAAGCGA[A/T]ATCTAATTAAAATGA | 10533 |
| rs549339816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362528 | GGAACACATGATGCA[G/T]TTCCATTATATGAGG | 10533 |
| rs549342479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545909 | TTTTGGGAGGCCAAG[C/T]CAGAGGATTGCTTAA | 10533 |
| rs549374176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436358 | AATTAGAAGCCTCCT[A/G]CCTACTAGTGGGAGT | 10533 |
| rs549387797 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11449409 | CTGAGATTTGGGGCC[G/T]GTAAGGCCCCAGAGT | 10533 |
| rs549399471 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369288 | GATGCAGCCCAGGAA[A/G]GGAGCCTCCTTTACC | 10533 |
| rs549405557 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11412161 | AAACTAGGGCTTTAT[A/G]TAGCAGGGAGGAAAC | 10533 |
| rs549407533 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372269 | AATATTCAGGGAGTA[A/G]CAAAGATACAAATAT | 10533 |
| rs549416226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347469 | TCATTCAGGCTTTAA[A/G]TGAGCTTCAAGAGTA | 10533 |
| rs549419540 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498489 | ACCTGCCTCTACCTT[C/T]TCATTCCTCCAATCC | 10533 |
| rs549433824 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306096 | CTCCTCTTCTCTTCT[C/T]CTGACTTTGCTTACT | 10533 |
| rs549458650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500520 | GGAAATTTTAAAACT[C/T]CCCTTAGGTCAACAA | 10533 |
| rs549466742 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395441 | TCCACACCAAGACCC[A/G]TCATAATCAAACTTC | 10533 |
| rs549469124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496153 | AAGGAGGACGTTATC[A/G]CTCTTTAACTAAAAA | 10533 |
| rs549470164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541038 | CCAAGTAGCTGGGAC[C/T]ACAGGTGCCCACCAC | 10533 |
| rs549472547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485747 | AGGGATCCAGTTTCA[A/G]CTTTCTACGTATGGC | 10533 |
| rs549505014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11535528 | AGGTGGTGACAGTGG[A/G]ACAGTAGCCCTGCCT | 10533 |
| rs549513942 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11272393 | TCATCGGGGCGCGCG[C/T]CTCAGAGAGAGCTGT | 10533 |
| rs549528010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389841 | ATTGACTCTGGATTC[A/C]CTGAAGCATTTGGAT | 10533 |
| rs549531726 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11437121 | TAGTTGGGGCATTTT[C/G]TTTCTCCTTCCCTCT | 10533 |
| rs549544243 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399516 | AAGAGGTAAGTAAGG[A/C]GTTGTAATGTAGAAG | 10533 |
| rs549549372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397893 | TTTGAGATCAGCCTG[A/G]CCAGCATGGTGAAAC | 10533 |
| rs549564201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475656 | CAAAGCAGAACATGG[C/T]AAGCTCCTGAAGGAG | 10533 |
| rs549569428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296413 | GATACCAAGTTAGGT[C/T]ACCTTTTATTTTAAA | 10533 |
| rs549570131 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11376839 | CACCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 10533 |
| rs549602922 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11370725 | GGTGGGTGGCCCAGA[A/G]AGAAAGAGGAACCTT | 10533 |
| rs549608992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376556 | TTTTGAGTCACAGAA[C/T]TCAGCATGAGGCAAG | 10533 |
| rs549609574 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273859 | TGGGATGGACAGTAA[C/T]TGGGGGGAAGCATAA | 10533 |
| rs549617679 | in-del | -/T/TT/TTT | 0.461148 | 0.133852 | intron-variant | ATG7 | GRCh38.p7 | 3:11440323 | TTCTGGCCTTTACTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10533 |
| rs549622777 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11393953 | CCCAAAGTGCTGGGA[C/T]TACAGGCATAAGCCA | 10533 |
| rs549631900 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557023 | GGTCATACGGTGTGC[A/G]GAGTCCACAAAGCCT | 10533 |
| rs549640807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398326 | GCTGGCATAGACGGG[A/T]TAATTAAACAAGTTT | 10533 |
| rs549648296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307218 | CCAGAGAGAATACTC[C/T]CAGCTGTCTCCTTCT | 10533 |
| rs549654452 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424960 | CCTCATTCTTTTAAT[G/T]GATGCAAAATATCCC | 10533 |
| rs549654748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11482037 | GGGCTTCAAGGAGCC[A/C]TTAATTCTCCACGTG | 10533 |
| rs549667605 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306231 | GTCAGGGGCTTGCCC[A/G]GCAGCAGTTTTGTGC | 10533 |
| rs549685828 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334937 | CCAGCCTGGGTGACA[C/G]AGCAAGACTCTGTCT | 10533 |
| rs549690499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440218 | GCTTCTAATAAAATC[C/T]GTGGGAATGAGATTT | 10533 |
| rs549690964 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468147 | ACTTTCATCCCTGCT[C/T]GCCCTTTGAGGTATG | 10533 |
| rs549695725 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11303803 | TTTTCGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 10533 |
| rs549700955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396739 | GTGAGCCGAGATGGC[A/G]CCACCGCACTCCAGC | 10533 |
| rs549701158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474887 | TGGGGGGCCGGAGCC[A/G]GTATGGCAGCAGTGC | 10533 |
| rs549722576 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11482793 | TATCATTTTTGTACC[-/T]TTTTTTTTTTTGAGG | 10533 |
| rs549729035 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451437 | GCTGGTCCTGACCTC[C/T]TGGCCTCAAGTGATC | 10533 |
| rs549750395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11531923 | AACATTTATTGAGTG[C/T]TTACTGTGTGCCAAG | 10533 |
| rs549754488 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11445663 | ATAAGCCTGCACATA[C/T]ACCCCTGAACTTACA | 10533 |
| rs549767811 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391947 | TATGCATAGAATTCC[A/C]TTGTACTTATTGGGG | 10533 |
| rs549769419 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11547191 | AGTAGTGAGAGAAAG[C/T]GGAAAAGGCCTCTTC | 10533 |
| rs549786306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452371 | GTCTGGGCGACAGAG[C/T]GAGAACCTGTCTCAA | 10533 |
| rs549794225 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11451833 | GGCTGCCCTGTCTCT[C/T]TCTATCTCTCTCTCT | 10533 |
| rs549797365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310206 | TGAAAAATATATAAT[A/G]TTAGCCATATTGATC | 10533 |
| rs549813604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484269 | TATGGTGGCGTGCAC[C/G]TGTAATCCCAGCTCC | 10533 |
| rs549818353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350811 | TCCAGTCTAGGCTGC[A/G]CACAGTGGCTGAAGC | 10533 |
| rs549818402 | snp | C/T | 8.30199e-05 | 0.00644229 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11358591 | GTGGCTTCCTGCCGT[C/T]ATTGCTGCAAGCAAG | 10533 |
| rs549823649 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11335110 | AGATTGACAGAGTAC[A/T]TCTGCTTGATCAAAG | 10533 |
| rs549826070 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11323756 | CTGTTAGTTGGGCTC[G/T]TTCTTCACTTAGTGA | 10533 |
| rs549855925 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386776 | TATGTATGATTGTGT[C/G]GTATAAAATATATCC | 10533 |
| rs549856099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11534128 | GGCACAGCCATGCCC[C/T]TTTGCCCAGGGCTTG | 10533 |
| rs549863261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316481 | TCTTATTGAAATTCT[A/G]TCTCCACTGTGAAGC | 10533 |
| rs549872402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331491 | TATGTTTTACAATGT[A/G]TCTGTTTCTATTTGT | 10533 |
| rs549875730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543098 | CTCCAACCGACCCCA[C/T]GGTGCAGGAGCAGCC | 10533 |
| rs549876874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508505 | TGTGGCCCAGGCTGG[A/G]ATGCAGTGGCCTGAT | 10533 |
| rs549880783 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417468 | TTGAAGTCTGTTCTA[C/T]CTGAAATTAATTCAG | 10533 |
| rs549884402 | in-del | -/T | 0.00370217 | 0.0428646 | intron-variant | ATG7 | GRCh38.p7 | 3:11422680 | TGCAAGAGGTTTAGC[-/T]TTTTTTTAGCATGTC | 10533 |
| rs549890697 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11507438 | CATCAAATAATGATC[A/T]AGTGTCAATTCTAAA | 10533 |
| rs549891757 | in-del | -/TTGTT | 0.000313871 | 0.0125234 | intron-variant | ATG7 | GRCh38.p7 | 3:11379948 | TGTGTTTGATGTGAA[-/TTGTT]TTGTTTTGTTTGTTT | 10533 |
| rs549902316 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11358008 | GTAAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 10533 |
| rs549907204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543842 | CGGACCTCTGGGGAC[A/G]GGAGGGGGAGGACCC | 10533 |
| rs549911818 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272443 | GCGGTAAGTGAGCCG[C/T]GGCGGGCGAGGGTGT | 10533 |
| rs549928120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11281101 | ATTCTTCCCTGATCA[A/T]GGTAGGAATGCAGTT | 10533 |
| rs549938740 | in-del | -/ACA | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11540295 | TGTAGTTCTCTGATG[-/ACA]ACATCTTTCCCGCAT | 10533 |
| rs549942167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455545 | ACAATTCCTTCTTCC[A/G]GTGACATCCATTTTT | 10533 |
| rs549942862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287599 | AAGATGTAGAATGCT[C/G]CTGATGCAGTCTTTC | 10533 |
| rs549952022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447092 | ATAGCAGTCATTTTC[A/C]GTGAAAAACCTTTTG | 10533 |
| rs549963650 | in-del | -/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293530 | AATGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 10533 |
| rs549969757 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11328485 | AATCTGTCTATTTGC[A/G]TTTAAGAAACGAACA | 10533 |
| rs549978539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11352721 | ATTGAAATACTAAAT[A/G]CTAAAAGGGATAAGT | 10533 |
| rs549983510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337264 | TTGAGACCATCCTGG[C/G]CAACATGGTGAAACC | 10533 |
| rs549994501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11512760 | ACAAAGCTTCCATAG[C/T]GTGGAAGGGGACCTG | 10533 |
| rs550006371 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11316395 | CTTTTTTTGTATCTT[G/T]GTTTTTCCTCGTGTT | 10533 |
| rs550017531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439570 | ACAAGCCAGGCTTTT[A/C]GGAGGCAGACGCAGT | 10533 |
| rs550031364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539082 | TACCACAAAATGTTA[A/G]TGATATCAACTGAGA | 10533 |
| rs550047293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326110 | AAGGAACTTCCCCCA[A/G]TGTCTTAGGATCAGT | 10533 |
| rs550052977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11351542 | GTGGGAGCAAGGGAC[A/G]CCATGCTGGGCCTGA | 10533 |
| rs550062452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392085 | CCAGAGGAATGTATT[C/T]CTTATGGTCATGTTT | 10533 |
| rs550087136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360115 | CAGTGGCGGAATCTC[A/G]GCTCACTGCAAACTC | 10533 |
| rs550091678 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11409722 | ATGTAGGTAGGTCTG[C/T]GATACATTTTGAGTT | 10533 |
| rs550096398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452932 | CAGTTCCTATCTGCT[C/G]GAAGTGCACGATTCC | 10533 |
| rs550106325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11534352 | ACACCAGCTTGCCAA[A/G]GTAAAGAAGGGCATG | 10533 |
| rs550115515 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11286569 | TTTTTGTCTTTTCTT[C/T]TCTTTCTTTCTTTCT | 10533 |
| rs550120864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461312 | GGGAATAGTGATTGG[A/G]GTCAGAAATGGCATC | 10533 |
| rs550126088 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11402241 | GTTCGAAACCAGCCT[A/G]GCCAACATGGTGAAA | 10533 |
| rs550128210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11528628 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAATAT | 10533 |
| rs550145090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527469 | ACCTGTCCCTGGGTA[A/G]CTATTTAATACCATA | 10533 |
| rs550147489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11464437 | CTTTCCATTAATGGA[A/G]TGTCCCAGTTGGTTA | 10533 |
| rs550147552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547022 | CTTTCGGCTGCCCAG[A/G]TTTATTCATGGTGCT | 10533 |
| rs550161947 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11361318 | GAGACAGAGTTTCGC[C/T]CTGTCACCCAGGCTC | 10533 |
| rs550167124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373221 | AGGCTTTAGTTTCCT[A/G]TGTGGATGGCAAAAC | 10533 |
| rs550169096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501309 | GAGTTATAAGAGGAA[A/C]AAGAAAATTAACCCA | 10533 |
| rs550175905 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399870 | AGCCACAGTGCCTGG[A/C]GTGGAAGCGACTTTG | 10533 |
| rs550182343 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455232 | GCCTTTTCATGAAGC[A/C/G]AGTTATTGATTTTAA | 10533 |
| rs550203264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11550005 | CTTTTCTTATTTGCC[A/G]TTATATTTCCTCTTT | 10533 |
| rs550205689 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11373934 | TCCAGATTTGAATAA[A/T]TTTGTAAGCTTTGGG | 10533 |
| rs550221464 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459098 | GACTGCTGGCCTAGG[C/T]GATCACTTCTCTCAT | 10533 |
| rs550230001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11276708 | CCTACTTTGTATTAT[C/T]TCTCTGGCCATTTGT | 10533 |
| rs550250051 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345143 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10533 |
| rs550255096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280057 | CTTTTCTTTTCTTTT[C/T]TTTTTTTGAGACAGA | 10533 |
| rs550262070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334635 | ATGCCTTAAAATGTG[C/T]GTGTGTGTGATGGGG | 10533 |
| rs550264533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418739 | TGTTTTCACACTACT[A/G]TCAAGAACTACCTGA | 10533 |
| rs550272076 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474487 | CGCCTGTGGTCCCAG[C/T]TACTCTGGAGGCTGA | 10533 |
| rs550284946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471403 | TGTGTGAGCTCCTTG[A/C]GAAAAAATATATGAC | 10533 |
| rs550309385 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461765 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10533 |
| rs550335758 | in-del | -/ATTCTAG | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11522652 | AGAATTTAGACTAAA[-/ATTCTAG]AGGTCATTTATACCA | 10533 |
| rs550337964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11363669 | TTTACATAGTAAATG[A/G]AAAAGCCAGGGTTTA | 10533 |
| rs550343395 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376567 | AGAATTCAGCATGAG[C/G]CAAGCTCAGGAAATC | 10533 |
| rs550343464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526598 | TGTTGATTATATTCC[A/G]CCAGCATTGTTGACC | 10533 |
| rs550352833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11415117 | ACAGTATGTAACTGT[A/G]ATGAACACTGTAGAC | 10533 |
| rs550360678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399684 | GGCTCAGACGATTCT[C/T]CTGCCTCAGCCTCCC | 10533 |
| rs550366570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450517 | TCACAAGAGATCAAT[A/G]TACAAATGAAGCAGT | 10533 |
| rs550374365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356154 | TCTGGGGGCAAGTGG[A/G]GACCGACTGAGGGGG | 10533 |
| rs550385922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474870 | TAAGGATGGGGTGGG[A/C]GTGGGGGGCCGGAGC | 10533 |
| rs550422601 | in-del | -/GCTAATTAACTGT | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11302189 | GATTTGGAATCTATG[-/GCTAATTAACTGT]GCTACTTCAATAAGC | 10533 |
| rs550428813 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430398 | CTTGATTCTCAATGC[A/G]TTTACAGGTGGTCAG | 10533 |
| rs550433168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317871 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 10533 |
| rs550434320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11520539 | TGGGGACATGGGGAT[A/G]AGGAAGATGCCGTGC | 10533 |
| rs550435971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328951 | AAAAATTAGCAGGGC[A/G]TGGTAACACATGCCT | 10533 |
| rs550447303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467565 | ATTTTTAGTAGAGGC[A/G]GGGTTTCACCATGTT | 10533 |
| rs550457631 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11533714 | TTTGAAGCCACAGTT[C/G]TTATTTCTTTTCTGT | 10533 |
| rs550459766 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420916 | GTATGCCACCTTGTC[C/T]GGCTAATTTTTTGTA | 10533 |
| rs550468362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490706 | TGCTTGTCTGTAAAG[G/T]ATTTTATTTCTCCTT | 10533 |
| rs550484465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405311 | GACTATTGGGCTGCC[G/T]GTTTTCACTGTGATT | 10533 |
| rs550491231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359454 | GTGGCTCACATCTGT[A/G]TCCTAGCACTTTGGG | 10533 |
| rs550495948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11450064 | CTTCTTTGGATAATA[A/C]TGATGTAATGGCTAG | 10533 |
| rs550500115 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11387275 | TCATGTCTCTTGACA[A/G]TGACAGCCAAAACCT | 10533 |
| rs550504602 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382367 | GAATACAGTGCTTTG[C/G]TTCTAAAGCAGGAAA | 10533 |
| rs550509377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468352 | CCGCCACTTCCCTGG[A/G]AGAACTGATGGCTTT | 10533 |
| rs550517394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511193 | AGCGGGTTGCCAATG[C/T]TGGCTCAGGCAGCCT | 10533 |
| rs550533141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486750 | TTTTTAGTATGAAGG[G/T]TTGTTGAATTTTGTC | 10533 |
| rs550535896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541120 | TTAGCCAGGATGGTC[C/T]CGATCTCCTGACTTC | 10533 |
| rs550554626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11377019 | GCTGGGATTACAGGC[C/G]TGAGCCACCGCGCCC | 10533 |
| rs550611096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11291503 | TGTGACTCTGGGCAA[A/G]TTACTTAAGCTCCCA | 10533 |
| rs550615014 | snp | C/G | 0.000239386 | 0.0109378 | intron-variant | ATG7 | GRCh38.p7 | 3:11340767 | GTTTTCTCCAGTCGG[C/G]CTTTTTGTAACCAAG | 10533 |
| rs550617821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284475 | AGTAGGTCATCTGTT[A/T]ACTGTTGGATGAATA | 10533 |
| rs550639846 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448078 | AGTCCCCAGATTTGT[C/T]CCCAAGCTTGACTCA | 10533 |
| rs550640483 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11497969 | ACTCGTCGGGTAGAC[C/G]TGAGCCTTCTTTGGA | 10533 |
| rs550645624 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11368737 | AGGGAGTCCCTGTCT[-/C]AAAAAAAAAAAAAAA | 10533 |
| rs550649625 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270534 | TTTGTGTGAGCAACA[A/G]GGCTGTTTATTTCAC | 10533 |
| rs550653117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11542730 | CCTGGGCATCCTCCC[A/G]GGCACCCCCTCCCGG | 10533 |
| rs550655294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11482162 | CGCTTCCTTCCAACT[A/G]GAAAGTTCATGAGAG | 10533 |
| rs550656645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283801 | GCTGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 10533 |
| rs550667400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482855 | TATCTTAAGTATACA[G/T]CTCACTGAATTTTTG | 10533 |
| rs550690102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553371 | CACAGAGCTGGCTAC[A/G]TGAATGTGTGTTCGT | 10533 |
| rs550698107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11341427 | ATTGTGTTTAAGGGC[A/G]AATCTCAGTGCACTC | 10533 |
| rs550715816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554054 | GCTCTCTCCCTGGGG[G/T]CTGACACCAAGGACT | 10533 |
| rs550740659 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298892 | TTTCCATCATCTTCT[A/G]TTATCCTCACGGTCC | 10533 |
| rs550742718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511665 | GTGCTCGTCGGGGAG[C/G]CTCCGGCCGCACAGG | 10533 |
| rs550744886 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272004 | GTCGACGTTCACTGG[C/G]CTTTTCCTACTAAAA | 10533 |
| rs550747185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278925 | GTGATGATTGAGCTG[C/T]GATTTGAAGTGAGCA | 10533 |
| rs550748683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11348841 | TAGCTAGACACAGAG[C/T]GCTGACTGATGCCTT | 10533 |
| rs550761795 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271033 | TCATCCCACTTCCCA[C/T]ATTCGGTTGTTTCCA | 10533 |
| rs550767580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499983 | CCTGATGGGCCACAA[A/G]CGCCACAAGTTCAGG | 10533 |
| rs550773365 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11396372 | TTGAGCCCAGAAGTT[G/T]GAGGCTGTAGTGAGC | 10533 |
| rs550784510 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11492856 | GAACAAACTTTGTGC[A/G]GACCCCACGGCAGTG | 10533 |
| rs550786397 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389813 | AAGTCTTGGCAGCTA[A/G]GGTGTCTTTGTAATT | 10533 |
| rs550823924 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411453 | ACATGGTGAAACCCC[A/G]TCTCTAAAAATACAA | 10533 |
| rs550827437 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11523000 | ATGGACACAATGATA[A/C]CTTTTAGGGCTTTTC | 10533 |
| rs550829183 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11355435 | GATGCCTTTCAAAGA[A/C]GGGAAAAACTAGCCA | 10533 |
| rs550855988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407794 | GAGTGTCTGGGATGC[A/C]GGGCACCAAGTCCTT | 10533 |
| rs550862580 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385071 | AGTCTTGCTCACTTG[C/T]GAGGCTGGAGTGCAG | 10533 |
| rs550863173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371675 | CCTCCAGGGACATTA[C/G]GCATTTGAGAACCAC | 10533 |
| rs550866403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321870 | AAGGAAAATTTTCTT[C/T]GATTAACCCCAGTTT | 10533 |
| rs550887996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377921 | TGATTATGCCTCAGG[C/T]CATGGATTATGAAAT | 10533 |
| rs550905257 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | ATG7 | GRCh38.p7 | 3:11390665 | TTGACCTTTGTGGGT[C/G]GGTTTGATTTTTTTT | 10533 |
| rs550915416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408405 | GTCTTCTTCTGAGCC[C/T]TCCAAACTGTTCCAA | 10533 |
| rs550916199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286655 | GAGTGCAGTGGTGCC[A/T]TCTTGCCACCTTGGC | 10533 |
| rs550920298 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483951 | TATTGGGATAAATTC[C/T]ATCATTACCCTAAAA | 10533 |
| rs550932091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437923 | ACCACCTAAAATCCA[A/G]TACATGTCCGAATTT | 10533 |
| rs550940647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323171 | AGCCAGCTCTTGTGA[A/G]GTAGGAATAGTCCTG | 10533 |
| rs550944872 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317603 | TTTTTTTTTTTTTTT[-/TT]GTTTTTGAGGCAGAG | 10533 |
| rs550946663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423146 | AATTGGCCTACATTC[A/G]GTATTGTTTTGTTGC | 10533 |
| rs550948098 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328356 | AGTAAGCTCTGTTTT[C/G/T]AAAAGTGCCCTAGAT | 10533 |
| rs550956450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11293613 | AGCACTTTGGTACAT[C/T]AAGGCAGGCGGATCA | 10533 |
| rs550989486 | snp | G/T | 1.69668e-05 | 0.00291258 | intron-variant | ATG7 | GRCh38.p7 | 3:11342103 | TTATTGCATAAAGGA[G/T]TGACTGAATAAGTAA | 10533 |
| rs551005827 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278262 | GCATAAGAAATTATA[A/G]AAGTATTAATTTTTG | 10533 |
| rs551006041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416493 | CAAATTTCTAGATAC[A/G]GAGTTGTTGATAGTA | 10533 |
| rs551014905 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300383 | ACACCTGGCCAAATT[C/T]AGAAAGCAGGGGTGA | 10533 |
| rs551019185 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523574 | TAAACGTTGATTTGC[C/T]TTTGGGAGGGCCAGG | 10533 |
| rs551020171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11444290 | GGGGTTCATGTGCAG[C/T]ATTTCTCTGGGTGTT | 10533 |
| rs551035758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11517636 | TTCACTAGAGGTTTT[C/T]GAGAGGAAGATGCAC | 10533 |
| rs551038780 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11463114 | GGTCTCAAACTCCTG[A/G]TCTCAGGTGATCTGC | 10533 |
| rs551048548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11488403 | GACAGCTCCGCTGCC[C/T]GCTGAACTCCATCCT | 10533 |
| rs551061629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11484391 | AGGAGACTCCGTCTC[A/G]AAAAATGAAAAAACA | 10533 |
| rs551068986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396883 | CATTGTCTTGGAAGA[C/G]GTTAAAGATAGGAAT | 10533 |
| rs551071990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484753 | CTGTGTCCATGTGTT[C/G]TCATTGTTCAATTCC | 10533 |
| rs551087915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11352634 | CTTCTACCAGGCCAC[A/G]GAGAAAAGGCTTGAC | 10533 |
| rs551094914 | in-del | -/GTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385044 | TTTGTTTGTTTGTTT[-/GTTT]TGGGACGGAGTCTTG | 10533 |
| rs551106686 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11440064 | TCTGCTTTATAGAAC[A/G]TATCTCTACTTTCAT | 10533 |
| rs551115707 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359051 | TAGAAAATGCCACAT[G/T]ATATTAAATAAGGAA | 10533 |
| rs551125610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308747 | CGGTGCTGAGATCTG[C/T]TGAGAGGAGGCGCCT | 10533 |
| rs551127501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381238 | CTCAAGGATGTCTGC[A/C]TGCACCCCCATCTTC | 10533 |
| rs551133003 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521121 | CAATGCTGAGACATA[G/T]TTCCAACAGATGACA | 10533 |
| rs551147004 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464695 | TGTGAAAGTCATTGC[A/G]AGTAGCTAGAAGCAG | 10533 |
| rs551154864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372004 | AAAGCGAGGCCAAAC[A/G]ACCTATTCTGATGCT | 10533 |
| rs551181303 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445130 | TAGTTAAATCGTTGT[A/G]GAAAGCAGTGTGGAG | 10533 |
| rs551183028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518728 | TGGCCCATACCCAAA[G/T]TGATAATCAGGATTG | 10533 |
| rs551188007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490581 | TCCATGGTCTTTACA[A/G]TTTGGCATGATTTTG | 10533 |
| rs551200502 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339800 | GTGTGGGAAACACAA[A/G]GCCAAATCAAATCAC | 10533 |
| rs551204644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11399611 | TGACAGTCTCACTCT[A/G]TCGCCCAGGCTAGAG | 10533 |
| rs551207224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554611 | CCCTGTTGGTTCCAC[A/C]AGGTGGTTCACACAC | 10533 |
| rs551208906 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11493712 | TAAATACTTAGATAC[-/A]AAAAAACAAAAGTTT | 10533 |
| rs551215090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286133 | TTTCCATGGCATTCT[A/G]TCAGATAGCACACAG | 10533 |
| rs551218114 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11457331 | TGCTGTGAACTGAGT[C/G]GTGTGGCAACTCTGG | 10533 |
| rs551220830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446884 | CATCGTGTTGTCCAT[C/T]TACCTCTGTGTATCT | 10533 |
| rs551233985 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11416521 | GTATTCTTTTATTAT[A/C/T]CTTTTCATCAATACA | 10533 |
| rs551240157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508778 | TTTTGAACTAATAAT[C/T]CTCAGTTCTGTGCCT | 10533 |
| rs551245445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466460 | ATTTCTTTCTGTTCT[G/T]CCAAGTTAGTTACTG | 10533 |
| rs551248960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11548135 | AGGCATGAGCCACCA[C/T]GCTTGGACTTTTGCC | 10533 |
| rs551255191 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467193 | TCTGCAGATTCTTTG[A/G]TTTCTCAGGAAGCCA | 10533 |
| rs551267254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11430954 | GCAAGAAGCCTAGGG[C/T]GTTCTAGACTGAATA | 10533 |
| rs551290253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374677 | TTGGGAGTCCGAGGC[A/G]GGCAGATCGTGAGGT | 10533 |
| rs551293187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387927 | GTGAACCAAGATCAC[A/G]CCACTGCACTCCAGC | 10533 |
| rs551302852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469857 | TAGCCAGGCATGGTG[A/G]CATGTACCTGTAATC | 10533 |
| rs551306215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329695 | AGAAGATAGTGGCAA[A/G]GACAGTACAGAGAAT | 10533 |
| rs551312632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459758 | TAATGAAACCATTGA[A/C]TTACAAACAAGAGTG | 10533 |
| rs551317708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312327 | ACCCACATATGTCTG[G/T]AATGCTACCATGAAT | 10533 |
| rs551321489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296765 | CTCTTCTTGTTCCTT[C/T]TGCCCTCCACCCATC | 10533 |
| rs551337062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420322 | AGCATTAAACTTTCT[A/G]TACATCCTCATTATG | 10533 |
| rs551337320 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556626 | CAACTTTTTTTTTCC[A/G]AACAACAAAAAAAAT | 10533 |
| rs551340966 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11412353 | AAGCTTTAACAGCAG[-/A]AGGGTCAATTTCCAT | 10533 |
| rs551344744 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468881 | GAGTGGACCTAATGT[A/G]TTTTTGTAATGTTTG | 10533 |
| rs551347709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289117 | TTTCCTTGACTGTGT[C/T]TGAATATAATGTTGA | 10533 |
| rs551348796 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11545914 | GGAGGCCAAGCCAGA[A/G]GATTGCTTAAGCCTA | 10533 |
| rs551365995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514229 | AAGTGGTTGAGTCAA[A/G]ATTGGAATCTGGCCA | 10533 |
| rs551370298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11556058 | CGCTGAAACTGCACA[C/T]GTACACTATGTGGTT | 10533 |
| rs551384190 | in-del | -/T | 0.49089 | 0.0668743 | intron-variant | ATG7 | GRCh38.p7 | 3:11418270 | CACCATACCTGGCTA[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs551384976 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11522768 | ATCGCCTGTCAAATG[-/C]CCACCCCAGGCCTAG | 10533 |
| rs551386107 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509185 | GCAATTATGACGCAG[C/G]GCCACATGGCCAACA | 10533 |
| rs551392194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441107 | GTAAACTGCTGTGGG[A/T]TATTTTTGTTTTGTT | 10533 |
| rs551399192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11513526 | CTGGCAGGGCCAGCC[A/G]GCCGCTCCCAGTGCG | 10533 |
| rs551417553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11352284 | GGTTCCAAGTCTTTG[C/T]TATTGTGAATAGTGC | 10533 |
| rs551462736 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11424700 | TTAAAAGTTAAAGTA[A/G]TATAAAATAATCTAC | 10533 |
| rs551479878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413986 | GGAATTTGTCTGTTT[A/C]ATCTAGGTTATGGTA | 10533 |
| rs551482733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304655 | ACAGCCCCAGCACTT[C/T]CCTGAGTCATCGCTG | 10533 |
| rs551489423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310880 | CTCGTGATCCGCCCG[C/T]CTCGGCCTCCCAAAG | 10533 |
| rs551498561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470744 | GGACATGGAGTAGAG[A/G]CCTTCCCTGAAGGGC | 10533 |
| rs551504583 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11494248 | TGCAGGAAAACAGGA[A/G]TTAGGGAGGGGTAAG | 10533 |
| rs551504670 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11448524 | TTACTTGCCGTGCTG[A/C]AACTTGTTGATAAAA | 10533 |
| rs551510427 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513299 | CGTGGAGCAGGGGGC[A/G]GTGCTCGTTGGGGAG | 10533 |
| rs551517890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374334 | CAGTTCAATTGGGAA[A/G]GAATGCCGTTTTCAA | 10533 |
| rs551520797 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556990 | CAAAATTCAACAGCT[A/G]AAAACTGTAAAACCG | 10533 |
| rs551527625 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11392131 | TGAAAGTCATGTGGG[C/G]TAGAGCAACTTCTAG | 10533 |
| rs551528506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311450 | ATCTACTAAAATTAA[A/G]AAAAAAAATTAGCTG | 10533 |
| rs551532550 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11440394 | CAGTGGCGGGATCTC[A/G]GCTCACTGCAAGCTC | 10533 |
| rs551540080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419685 | GCCGAAAATTAGAAG[A/G]GTGTGGGGGCGCTGA | 10533 |
| rs551555809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11435179 | TATTCTTTGGTATCT[A/G]TTATATCTAGCTACC | 10533 |
| rs551559128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326915 | CCCAGGGTTAAAATG[C/G]CATGAGACCCTGTAA | 10533 |
| rs551564219 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535787 | GCCTTCCCAAGAGCC[C/T]TCTGGGGCATTTCAG | 10533 |
| rs551567849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11436138 | TAAAGATACAGAACT[C/T]AATTAAAAATGGGCA | 10533 |
| rs551574383 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11546359 | GTATTTTTAGTAGAG[A/G]GGGGGTTTTGCCATG | 10533 |
| rs551584403 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553751 | AGGCTGCCTCCCCTC[A/T]GCCTGGGAGCTGGGT | 10533 |
| rs551589121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11545118 | GAGCCAGGAGGCTGC[A/G]GCCGCTGGAATCTGG | 10533 |
| rs551592030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326235 | TTTGGAAGTAGAAAT[A/G]CTAGTTTCTCCCTTC | 10533 |
| rs551606073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11496766 | TATCATACTTTCTGA[A/G]GCTGGAAAAGAAAAA | 10533 |
| rs551624109 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11387358 | TTTAAGACTACCTAA[C/T]TAGTAGTTAGAACTT | 10533 |
| rs551647326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313128 | TATTTTGGGAATACA[A/G]AAGTCCTTTATTTGA | 10533 |
| rs551648075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299223 | TCCATACATATATTA[C/T]CTATGTAGCATAGAT | 10533 |
| rs551649646 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | ATG7 | GRCh38.p7 | 3:11306117 | TTTGCTTACTCTGAG[G/T]ACTGTGAGGCCTTTG | 10533 |
| rs551670531 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11316314 | TCCTCATAAAGCATT[A/G]CTCCAGCTAATCTTA | 10533 |
| rs551671174 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11434162 | TGGCCTCTCCCCCAC[A/C]CAGCTGGTTTTGATT | 10533 |
| rs551671553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529070 | ACTGTGGAAAAAAGG[A/G]GGCGGTACATTCAGG | 10533 |
| rs551673553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521710 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 10533 |
| rs551680495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290884 | GAGACGGGGTTTCGC[C/T]ATGTTGGTCAGGCTG | 10533 |
| rs551682575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347420 | AAAATATCATACAGT[A/G]GGAAATAATTTGTGA | 10533 |
| rs551683902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11306751 | GGAATATATAGGCTT[C/T]TAGGGGGGAATGGTG | 10533 |
| rs551697256 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558161 | AAGCTGAGCCACACA[C/T]ACCCCGGTCTCAAGA | 10533 |
| rs551701707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332469 | AATGTTTATTTAAAA[A/G]TATGAAGATAGATAA | 10533 |
| rs551728253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515662 | TGCACGGCCACATGT[A/G]TACATTAAGCCTCAT | 10533 |
| rs551737708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369617 | GGAGGCCTCTGAATA[C/G]AAGGAAGGATCCGGG | 10533 |
| rs551743601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530531 | ACAAGAAAAACCCCA[A/G]TTCTTTCCAGTCGGC | 10533 |
| rs551755004 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11445932 | TTACTTATTTGGATT[A/C]TTCTTTTCTGATAGT | 10533 |
| rs551788350 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11410034 | GTCCTTTAATATTAT[C/G]TTGGCTTATCTGGGT | 10533 |
| rs551819973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442324 | TTCATCTTGCCTGGA[C/T]TTCATCTGTAAAATG | 10533 |
| rs551821189 | in-del | -/CA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11425087 | CCCACTTTAGCTTCC[-/CA]AGTAGCTGGAATTAC | 10533 |
| rs551844934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450747 | ATGGGCCCTGCTACC[A/G]TTTGTGAACAGTCTT | 10533 |
| rs551849614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11504041 | ATTGAGAGAAACAAA[C/T]GTCTCCATTGAGAGA | 10533 |
| rs551849779 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11509267 | TGGTTGGCTGCTGCC[-/G]GCAGGAGGGAGCCGA | 10533 |
| rs551860449 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11420804 | CTTGTTGCCCAGGCT[G/T]GAGTGCAATGGCGCG | 10533 |
| rs551861735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545841 | AAACTAGCAGCCTCC[C/T]GCAGAAGAAGTGGGG | 10533 |
| rs551863247 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11534449 | CTGCTCACAGGCAGG[G/T]CCTGTGTTGCCCTGT | 10533 |
| rs551864479 | snp | A/G | 4.96134e-05 | 0.00498039 | intron-variant | ATG7 | GRCh38.p7 | 3:11306924 | TGTGCCTGACTAACC[A/G]TGTTTCTCTTGTATC | 10533 |
| rs551872349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491415 | CTTTGCCTTTGGTTT[G/T]AATTTCCTCCTGTAG | 10533 |
| rs551872833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409085 | TGTAAATAGTTTCTC[A/G]TGGCCTGCAGCTGGT | 10533 |
| rs551929559 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332005 | AATTAAAAATATCTA[C/T]GGCTCAGCAATGTTA | 10533 |
| rs551946577 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11499266 | CATTCCTCTATCCTT[A/T]CCTGTTCTACATGGG | 10533 |
| rs551950487 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11542177 | CACTTGGTAGATCAG[A/G]AGCTGAGAGCCCCAA | 10533 |
| rs551953001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300049 | CGTGCCTTAGCCTCC[C/T]AAGTAGCTGGGACTA | 10533 |
| rs551958321 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11388718 | CAGGTGTGAGCCACT[A/G]CGCCAGGCCCCTTCT | 10533 |
| rs551967625 | snp | G/T | 1.65507e-05 | 0.00287664 | splice-acceptor-variant, intron-variant | ATG7 | GRCh38.p7 | 3:11554810 | CCCCTTCTCCATGCA[G/T]ATCTGGGACATGAGC | 10533 |
| rs551981956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343053 | CCTGCCTCAACTTCC[C/T]GAGTAGCTGGGACTA | 10533 |
| rs551989239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536739 | AGCAGCGAAGGACCA[C/T]CCTGGTCTGGTCACC | 10533 |
| rs551996811 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11421874 | AAAACAACATTTATC[C/T]CTTTGTACATCTCCA | 10533 |
| rs552003453 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11278727 | AGGTGCTAGAAAAAC[-/AA]TGATGAATGGGGGAA | 10533 |
| rs552018674 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471646 | GGTCAAATGGTATAA[A/G]AAATGCAGGTGGCTC | 10533 |
| rs552031912 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396338 | CAGCTACTTCAGGGG[C/G]TTGAGGTGAGAGGAT | 10533 |
| rs552043428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308895 | GTAGGAAAGAAGAGC[C/G]TGGTGCTTTTCAGCT | 10533 |
| rs552063315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11486017 | TTAGGATTGACTTGG[C/T]GATGCGGGCTCTTTT | 10533 |
| rs552075846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11481545 | GTTATGAGAATATTA[C/T]CTAAGATCTTATCTA | 10533 |
| rs552077876 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557553 | CAGGAGCTGGCCTCC[C/T]GCACTACTTGTGAGT | 10533 |
| rs552085172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445469 | TATCACTTATAAGTG[A/G]GAGCTGAATCATGAG | 10533 |
| rs552089095 | in-del | -/T | 0.0600896 | 0.162586 | intron-variant | ATG7 | GRCh38.p7 | 3:11422680 | GCAAGAGGTTTAGCT[-/T]TTTTTTTAGCATGTC | 10533 |
| rs552093075 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11378754 | TTTTTTTCCAGAGAG[A/G]AGTATGCACAAACAG | 10533 |
| rs552101463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485674 | GTTTTTATGGTTTTA[A/G]GTCTAACATTTAAGT | 10533 |
| rs552107119 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419731 | AAGATAGGTTTGATA[C/T]AGTAAAGAGTAAGGA | 10533 |
| rs552115516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480614 | GTGCTCACTGGTTTC[C/T]TCGACTTCACCTAAA | 10533 |
| rs552120364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351186 | CCGTGTTCCAGGGAC[A/G]GGGGAACTAGACAGA | 10533 |
| rs552131659 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11371908 | GCTAATTAGACACGC[A/G]CAGGTGTGCCTAATG | 10533 |
| rs552139160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549897 | CAGACATCGGGCATC[A/G]CTGGCCTTTAGCTTC | 10533 |
| rs552139775 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11537371 | TTGTGTTAGTCTCTT[G/T]TCACCTCCACTAGGC | 10533 |
| rs552142499 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484271 | TGGTGGCGTGCACCT[A/G]TAATCCCAGCTCCTC | 10533 |
| rs552155606 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303126 | TAACAACAGATTAAT[A/G]AGGAAAGACAGCCAA | 10533 |
| rs552160067 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11410527 | CAGTTATCACCACCA[C/G]TTACCTTCACAATTC | 10533 |
| rs552163870 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271979 | GTTTAGAAAAGGCAG[A/G]TTGGTCACTGTCGAC | 10533 |
| rs552174975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11317407 | TAACAGTTTGAACAG[C/T]GCTTTACAATTAATT | 10533 |
| rs552214729 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554973 | CGAGGTCTGGGATTC[C/T]CCCCTCTGCTGCCCA | 10533 |
| rs552227664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329660 | ATAAACTTTTTATTT[C/T]GGGATAATTTTAGAT | 10533 |
| rs552236311 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ATG7 | GRCh38.p7 | 3:11488466 | TCGCGGCAGCGGCTC[C/T]GCTTCATATCTGCAG | 10533 |
| rs552243338 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288324 | CATTGGCCCTTTGTG[C/G]GAAAAGAGAGCTATT | 10533 |
| rs552252083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542539 | CCTTGCCATGGGCCA[C/T]GGCCCTTCCTGTGGC | 10533 |
| rs552257562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337079 | GACACTGCTGCGGGT[A/G]GAGATCCCATCTTAA | 10533 |
| rs552266330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323121 | TTAGAACATGTTAAG[G/T]TTCATAATCAGTGGT | 10533 |
| rs552312975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291142 | ATGATGAAAACAAGT[G/T]ACATTTGTCCTTGAA | 10533 |
| rs552321663 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313787 | TGTCTTTTAATAGAT[A/G]TGGGGTTTTGCCATG | 10533 |
| rs552326555 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352783 | ACCTGGACAAGTGTG[G/T]GGCATGTGCCAGGGA | 10533 |
| rs552337372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367140 | ATAGGCTTTAAACAA[A/C]TTTTTTCCCCCTAAG | 10533 |
| rs552346405 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11350663 | TACCAAAGCGAGTCA[C/G]AGGACCAAGCCCAAA | 10533 |
| rs552350117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11371557 | TTAAATCAGAAGACA[A/G]CCTAATCCAGGGATT | 10533 |
| rs552350359 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11295073 | GCCGAGACTGTGGCA[C/G]TGCACTCCAGCCTCG | 10533 |
| rs552356160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391381 | GATGAATTCTCATTT[C/T]CTGGAGGCTGAAGAT | 10533 |
| rs552378160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359322 | GTTTATTCTTATTTT[C/T]CAAACTTTCTATATA | 10533 |
| rs552379735 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11399760 | TTTATTTTTAGTAGA[C/G]ACAGAGCTTCACCAT | 10533 |
| rs552395637 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11342062 | TTATTTTCTTGCATA[A/G]CCACTTGAAATCTTT | 10533 |
| rs552405538 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456718 | CCACAATTACTGTTT[A/G]GACTCAAAAATGTGA | 10533 |
| rs552409404 | in-del | -/GG | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11390661 | CTTTTTGACCTTTGT[-/GG]GTGGGTTTGATTTTT | 10533 |
| rs552433569 | snp | A/C | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11331387 | AGCCCAGTACCCTGG[A/C]TGGCCTTTGAGGAAT | 10533 |
| rs552433592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457904 | ACCCTCAGGACCGGA[C/T]CTAGTGCATTGCCTG | 10533 |
| rs552441258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317783 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATATTG | 10533 |
| rs552460765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328271 | ATATTATTTCCTCCA[C/T]GATTAAACTGTGGCT | 10533 |
| rs552484128 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11330409 | GGGTTATAATTCAAC[A/G]TCATATTATTTATAT | 10533 |
| rs552486451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538982 | GAGAGCATGGAGAAG[A/G]GATCTGAGCTTCTTG | 10533 |
| rs552495228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458408 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 10533 |
| rs552499492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366412 | CATTTTTTTTTGACA[G/T]GCATGTGTTAATCTT | 10533 |
| rs552502026 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11371772 | GGTAGCACACCAAAT[-/C]CTGCTTTTTGAATTT | 10533 |
| rs552511284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11274169 | TTACTCAACCACAGG[C/T]TCCGTTTTTCGTTCC | 10533 |
| rs552513276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452802 | GAGATAATTATTGCA[A/G]ATATTAGTGTTAAGA | 10533 |
| rs552514448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11489152 | TGTATGTGTCGAGGA[A/G]TTTATCCATTTCTTC | 10533 |
| rs552515198 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | ATG7 | GRCh38.p7 | 3:11490682 | GTGGTGACAAAATCT[C/G]TCAGCATTTGCTTGT | 10533 |
| rs552517605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459833 | TGTTTGGTAGACTTT[A/G]GCCAGGCCACGTATA | 10533 |
| rs552523909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368694 | AGTGAGCCAGTATCA[C/T]ACTACTGCATTCCAG | 10533 |
| rs552541275 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11350868 | GAAGTGGGAGGAGAT[C/T]GCTTAAGGCCAGAAG | 10533 |
| rs552551098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431174 | TGGGAGGCCGAGGTG[C/G]GTGGATCACTTGAGG | 10533 |
| rs552551350 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372658 | CCCAATTTCTATATG[A/G/T]ACCATTTTTATTTTT | 10533 |
| rs552569349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11507197 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 10533 |
| rs552583937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330653 | TTAGAAGTCAGTATC[C/T]GGGTGCTGGGTGCTC | 10533 |
| rs552586066 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11418023 | TCACTGTGTTAGCCA[A/G]GATGGTCTCGATCTC | 10533 |
| rs552607578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11507772 | AGCCCAGCAATTTTA[A/G]GTCCACACTCTAGAT | 10533 |
| rs552629538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287546 | GGTCTGGGAGAAAGC[A/C]TAAGGAAACCATCAG | 10533 |
| rs552631898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477964 | TCTATCTTCTACCTT[G/T]CATAAGTCAGTCTCG | 10533 |
| rs552640884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466086 | CTAAAGTCTGCGGCT[C/T]ATTCCTAATGTGGAA | 10533 |
| rs552643267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11373096 | TGTTTAATGCTTACC[C/G]TACTATAAGGAGAAA | 10533 |
| rs552655393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458980 | GCAGCTTATGAGATT[C/G]TAACACCTGATGATC | 10533 |
| rs552657020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466729 | TCAATATCATCTATA[C/G]AAACTCAACTGTTGG | 10533 |
| rs552657881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11503144 | CCTCTGACCAGCTCA[A/G]AAGAGCAGTTGTCGG | 10533 |
| rs552666207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286903 | AGCCACCGCACCCAA[A/C]CTTTTTTTATTATTA | 10533 |
| rs552685889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374555 | TACCAAAAGACCAAG[A/C]AATGTAAGAAAAAAT | 10533 |
| rs552693594 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11452292 | TGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 10533 |
| rs552696889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384776 | GACCAGCCTGGGTAA[C/T]ATGGTGAAATCCTGC | 10533 |
| rs552711509 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410231 | TTTAGATTGTCTCCA[A/G]CTTCTCTCAGCAGTA | 10533 |
| rs552741661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11496191 | CACAGAGAAAGGGTT[C/T]GGCATTGGCAAGGCC | 10533 |
| rs552761885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332751 | TCACCTAGAAAGAAA[C/T]CACAGCCAATTCATT | 10533 |
| rs552775584 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11378155 | AGGAGCTGGGATTAC[A/G]TGGGTGCACCACCAC | 10533 |
| rs552778182 | in-del | -/TGTGTGTG | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527042 | GTGTGTGTGTATATA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 10533 |
| rs552788053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273144 | TTTTTTAAAAATTGG[C/T]AAGTAATTCTGGCGT | 10533 |
| rs552788580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380974 | TATTTTATGGGAAGC[A/G]CAATCCTGACCAGTT | 10533 |
| rs552800249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543799 | CCCGGCTACTCAGGA[A/G]GCTGAGGCACGAGAA | 10533 |
| rs552816695 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11324525 | ACCATTTTCAAGCTG[A/C]CCTGCTTTTATGGGT | 10533 |
| rs552831720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525847 | GTGTGAGCCACTGCA[C/G]CTCGCCAGTTATAGC | 10533 |
| rs552835261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538325 | TTCAAGGGATAGCTC[C/T]CTTGGCAAAACACCC | 10533 |
| rs552840979 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11454965 | GTTTTTAAAATATTA[G/T]CAAAACTAGATAGCA | 10533 |
| rs552857475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494673 | CATCTCTTGATGGAA[C/T]ACAGATATGGAGGAC | 10533 |
| rs552860802 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512340 | GAGTTCCACCTCTGG[A/G]TCAAGGGCTCCAGAG | 10533 |
| rs552877445 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488797 | ATGTGCTGCTGGATT[C/T]GGTTTGCCAGTATTT | 10533 |
| rs552893465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501156 | CTACCTGGGATGCTG[A/G]GGTGGGAGGATCACT | 10533 |
| rs552901736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453263 | GAAAGTGTGGAAAGG[C/T]CTGTCCCCAAGCTTT | 10533 |
| rs552904389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510543 | AACCCCCCATCTCCA[A/G]AGCTGTCCCCTCGCT | 10533 |
| rs552911111 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11460025 | TTATCTTACTGCAGT[A/C]ACACAGCTCAGCATC | 10533 |
| rs552911420 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11413172 | TTATTTTCCTTGACT[C/G]ATTTCTCTGGCTAGA | 10533 |
| rs552917438 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351072 | TTTACTCAAATCCTA[A/G]TCATTGTCAGTGACC | 10533 |
| rs552922202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275824 | CACTCCATCTCAGAC[C/T]GGCTTCAGAATGATC | 10533 |
| rs552925854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11411790 | TTAAGAAATCATTGC[C/T]AAATCCATTGTTGTG | 10533 |
| rs552948109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406875 | CCATAACATATGGGA[A/C]TTATGGGAGCCACAA | 10533 |
| rs552949249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283930 | GAACGAGACTCTGTC[G/T]CAAAGAAAAACAAAC | 10533 |
| rs552970666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453687 | TATGAAAACAGACAA[C/T]TCACATTGCATTGTG | 10533 |
| rs552975354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327047 | CTGCTCTAGCTGCCT[A/C]CCAGGATCCCTGCTC | 10533 |
| rs552979484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406192 | ATGGGGTTTCATCAT[A/T]TTGCCAAGGCTGGTC | 10533 |
| rs552985648 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455467 | ATACCTCCTTCAGAG[C/T]AGGGCATCTGAGCCT | 10533 |
| rs552986462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291136 | AAAATTATGATGAAA[A/G]CAAGTTACATTTGTC | 10533 |
| rs552988517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11510966 | GCTCTTAAGGTGGCG[C/T]GTCTGGAGTCTGTCC | 10533 |
| rs552990444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11503743 | CCTGGGCAACAGACC[A/G]AGACTCTGTCTCAAA | 10533 |
| rs553010128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11502331 | TGCACCCACTAACTC[A/G]TCATCTAGCATTAGG | 10533 |
| rs553011478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400613 | TCACACCGCACCCCC[C/G]ACCCCAAAATACTGC | 10533 |
| rs553026220 | in-del | -/TG | 0.0147011 | 0.0844655 | intron-variant | ATG7 | GRCh38.p7 | 3:11334632 | ATATGCCTTAAAATG[-/TG]TGTGTGTGTGTGATG | 10533 |
| rs553032146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283137 | TCGCTGCCCTTTAGA[A/G]CTTGTTCTTTTGGAC | 10533 |
| rs553034391 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422345 | TGTTGCAGCTTCTAC[A/C]TCAGTACTTGCTGCT | 10533 |
| rs553034659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281632 | ACAAAAAATTACCTG[A/G]GCGTAGTGGCGGGCG | 10533 |
| rs553042652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318895 | TGGCTGATTGCTTGC[A/G]CCATTTCATTTCTCT | 10533 |
| rs553046005 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519138 | GTTATTATTTGAAAA[A/T]ATTGTGGCCTCTAAA | 10533 |
| rs553068121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388874 | CATCAGCTGGAACTG[A/G]GAAAGCTTTTATGGA | 10533 |
| rs553073361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419961 | TTCAGAATATTTACA[C/G]CCTTCCAAAATGTAA | 10533 |
| rs553091839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448674 | GGTTGTTGTTGAACA[A/G]ATTGCTGCCAGATGT | 10533 |
| rs553105717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289413 | ATAGATTGTCCTGTT[A/T]AGGTATTTCCAGAAG | 10533 |
| rs553119189 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399666 | TGCAACCTCCACTTC[C/G]CGGGCTCAGACGATT | 10533 |
| rs553124850 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11347328 | GTGAAAACTATTTCT[A/G]AGAATATAGACTTGT | 10533 |
| rs553124858 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11521462 | CACAGCAGGGCACGG[A/G]GAAGGAGCAAGCCAA | 10533 |
| rs553156697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313456 | TGCACATAAAATTGG[A/G]TTGAATGTGCAAGAG | 10533 |
| rs553161626 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317196 | TTTATTAAAATTCTT[A/T]CCCCCAGGTGATTTC | 10533 |
| rs553163012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442023 | GCCCAGGCTGGTCTT[A/G]AACTCCTGGCCTCAA | 10533 |
| rs553163697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11401128 | AAATAAAAACTCTCA[C/G]ACCCCGCCCCAGACC | 10533 |
| rs553180438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436523 | AGCCCTGTTCCACAA[G/T]GAACAGTACCAAAAA | 10533 |
| rs553189173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480776 | ACACAAATCTGTCAA[A/G]GAAGGCTTTCCTGGG | 10533 |
| rs553191097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511583 | CTGCCTGCCAGTCCC[A/G]TACTGTGCGCTCACA | 10533 |
| rs553194884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415955 | ACCACAAACATGGAA[G/T]TAATGTTGTTGCACT | 10533 |
| rs553201261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474595 | ACAGAGTAAGCCCCT[A/G]TCTCCCCATCTCAAA | 10533 |
| rs553215138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284612 | GCTGGAATACAGTGG[G/T]GCAGTCATGGCTCAC | 10533 |
| rs553224513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442419 | AAACTAAATACAAAC[G/T]AACCAAATGGAAAAC | 10533 |
| rs553234992 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392834 | GTAGAAACTGGTAAC[A/G]TCCTATATTAGAAGT | 10533 |
| rs553239995 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551620 | ATTTTTATAGAGAGA[C/G]GGTCTTGCTCTATTG | 10533 |
| rs553251802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291893 | ATCAGGAAACTAGCA[A/G]GCTAAGGCTGCAGCA | 10533 |
| rs553267221 | in-del | -/AGTA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11405601 | TTATATTTTACAAGT[-/AGTA]AGTATGTAGCATTTC | 10533 |
| rs553281543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319558 | AACCATTTCCTCCCA[A/G]GTAATTCAATTTTCT | 10533 |
| rs553303104 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304326 | AATTGAATTACAAGC[A/G]GTCTAAGCGCATGGC | 10533 |
| rs553305004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511895 | GCTGCTCCGAATGCG[C/G]GGCCCACCAAGCCCA | 10533 |
| rs553305996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534945 | CTTTGTGACTTCCTG[C/G]CAGAAGCCTCCACTC | 10533 |
| rs553308990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492194 | AGCCCATCGGAAAGG[C/T]GCAGTATTAGGGTGG | 10533 |
| rs553350807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276776 | GTCCCTCACATGCCA[A/G]TTTTTGCCAAGACTC | 10533 |
| rs553351600 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11416134 | ATTTTAAGATTCTTA[C/T]ATCTATGTTCATGAG | 10533 |
| rs553381681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375922 | AAAATGTTAAACAGT[C/T]GTCATATGACCCAGT | 10533 |
| rs553381936 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11472504 | GGGTTAGGGGTGGAA[C/T]AGTCCCACCTAAGTC | 10533 |
| rs553384073 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11338093 | CTAGTATTTTTTCTG[A/C]TCCTCTCCCTCCTCC | 10533 |
| rs553389094 | snp | C/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271375 | ACAGGCGCCCGCCAC[C/T]ACGCCCGGCTAATTT | 10533 |
| rs553390775 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306710 | TGGGGGACAGTAGAA[C/G]AGCATCCTGATAGGT | 10533 |
| rs553391047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11512163 | CTGTCACCTCTCAGC[C/T]TCACCCACCCAGTGA | 10533 |
| rs553393478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340495 | GTGGAAATTCAGGCC[C/T]TCAAGTCTCTTTTAG | 10533 |
| rs553422695 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11423643 | TTCCAGGGGGTTAGG[C/T]TGTCAAATTAATTTC | 10533 |
| rs553428088 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11489092 | CAGAGCCTGTTATTG[A/G]TCTATTCAGAAATTC | 10533 |
| rs553428287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11552997 | ACAACCCCAACCACC[C/T]ATTTGCAGAGGGCAC | 10533 |
| rs553433660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391155 | GCCATAAAAAACTTT[C/T]CATCTTTAGAAGTTG | 10533 |
| rs553442954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518624 | CTCTGTTTCTTTGCT[A/G]CATCAGACTTTGACC | 10533 |
| rs553456929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339930 | GATATAAGTATAGAA[A/G]CATTTCCAAAGTCTG | 10533 |
| rs553457916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11299635 | TATTTATCAGAGTCA[A/G]TTAGGTGCCAGGTGC | 10533 |
| rs553464672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518046 | ATATAGAATGTACAG[C/G]CTCTGGTGATTGGTT | 10533 |
| rs553472692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391839 | AGAGAGCATTAGGCT[C/T]AGAGAAATTACATGA | 10533 |
| rs553474736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11294507 | GGATTACAGGCGTGA[A/G]CCACTGAGCCTGGCC | 10533 |
| rs553493518 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557730 | CCAGCTATTTTTTCT[C/T]CATTAAAACATGCAT | 10533 |
| rs553498313 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11431731 | TTTTCATTTAAAGAA[A/G]AAGTCTCAATGCTAT | 10533 |
| rs553507257 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | ATG7 | GRCh38.p7 | 3:11553728 | TCGGGAGACAGGGGC[-/A]AGTGAGAAGGCTGCC | 10533 |
| rs553510709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549048 | TGAGGTTCTTGCCAG[C/T]GTTATCTCAGTGCAG | 10533 |
| rs553512813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478132 | CCTGTGACCGACAGT[C/G]TTGTTAGAGACATTA | 10533 |
| rs553530221 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423312 | ATAGTAACATCAAAG[A/G]CCACTGATCACAGAT | 10533 |
| rs553530330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552524 | CTGTCCCTATCCCCA[A/G]GAGTCCCTGTTCTGG | 10533 |
| rs553543712 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11348308 | TCAAGAATGAAGCCG[C/T]GGACCTTCGCAGTGA | 10533 |
| rs553574414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11321265 | AGGAGGTGAATGAGT[C/T]CTCTTTGTTCCAAGT | 10533 |
| rs553575701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370522 | TTTTATTTATGCGAA[A/C]TCCAAGCTTTAGAAA | 10533 |
| rs553578750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498645 | CCTGCTGGCCAGACT[A/G]GTGAGGCCAGGTGTC | 10533 |
| rs553580927 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452986 | CAGTCCATTGGGCCC[A/G]ATTACTGCTGACCTG | 10533 |
| rs553582543 | in-del | -/A | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11435019 | AAGCCTCCTTTCTAG[-/A]AAAAAATGAAATGCT | 10533 |
| rs553591460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325016 | TATGTGTTTAGATTT[A/G]TTCAGATACACAAAT | 10533 |
| rs553599094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421883 | TTTATCTCTTTGTAC[A/G]TCTCCATCAGACCTC | 10533 |
| rs553614385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371158 | CCTCCATTCTCTGGG[A/G]TATCATTTTCCACAT | 10533 |
| rs553614409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11363174 | TTTTATTTTTCCAAC[A/G]CTTATATAGGGCTTA | 10533 |
| rs553628875 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11434052 | TTACGGTCATGTGAT[A/G]TGACTTCATTGGCAC | 10533 |
| rs553634997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328641 | ATTCATTTTCAGAGA[C/T]TGAGCAGATGAAGAC | 10533 |
| rs553642657 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450458 | GGTCAGAAAATCTTG[A/C]CAGTTTATAAAGATT | 10533 |
| rs553654273 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462834 | GGCCCTGGCTCCTCT[C/T]AGATATTTTTATTTA | 10533 |
| rs553661990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376726 | GGAATTCTCTGCCTT[A/G]TTTATTATTTATATT | 10533 |
| rs553684350 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11536722 | GGCTCCGACCGGGGC[C/G]GAGCAGCGAAGGACC | 10533 |
| rs553685006 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11460911 | CCAGAGGGTGTGTGT[G/T]TTGAGAACCACCTGG | 10533 |
| rs553686197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384922 | CACTATAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 10533 |
| rs553693314 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295386 | GATTTCTGTTGCCAA[A/C]ACATCTTTTTAAATG | 10533 |
| rs553694995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467936 | CCTCCCCCAGTGTCA[C/T]GGCTAAATTTATATA | 10533 |
| rs553710337 | snp | A/G | 0.000264375 | 0.0114943 | intron-variant | ATG7 | GRCh38.p7 | 3:11446492 | AAAATACTTTATTGT[A/G]TCTGGTTTACTTTTA | 10533 |
| rs553711668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11280208 | CCTGCCACCATGCCC[A/G]GCCCTTTTTTTGTAT | 10533 |
| rs553737933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370260 | AGTGGTTGGGAAGAT[G/T]TGCTCCATTCTGCAG | 10533 |
| rs553750692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337384 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 10533 |
| rs553761852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336734 | AGTGAGTGCAGTGGC[A/C]AAATCATAGCTCACT | 10533 |
| rs553773509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11440616 | GGCGTGAGCCACCGC[A/G]CCCGGCCTTTACTCT | 10533 |
| rs553779144 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11395390 | CCTCAAATCCAAGAA[A/G]CCCAACAAATTTATA | 10533 |
| rs553782162 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11483397 | CACTGAGCTCCCAAC[A/G]CGCACAGATCTTGCT | 10533 |
| rs553817314 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11302567 | CCTCTACTGTATGAG[A/T]GAGAGAAGTAGAAGG | 10533 |
| rs553821991 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519551 | GGAGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10533 |
| rs553825991 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555093 | CTGGGACTTGGTCCT[C/G]CATGCAGTTTTTATT | 10533 |
| rs553826959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317506 | TGGTTAGTTAATTAG[C/T]ATCTGCATTTTCTGT | 10533 |
| rs553845897 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11333354 | CCCCTCTGCTCCCCC[C/T]GTTTTCAATTTTACT | 10533 |
| rs553853494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532964 | CACTGCCTCACATGA[A/G]CACCGTGCCCCAGGA | 10533 |
| rs553853549 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400380 | CAATAAATCAATGAG[C/T]AGAGAAGGACTAGCT | 10533 |
| rs553856741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11342588 | AAATCAGTATCTTTG[C/T]TGATATTTATTTGTA | 10533 |
| rs553857769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318113 | TGAAAGACAACAAAT[C/G]TCTGGGGTCTCCTCT | 10533 |
| rs553858437 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11496525 | GCTGCTGAGGCTGGG[A/C]CTTTGTGTCCTCGCT | 10533 |
| rs553860461 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11350957 | AAAAAAAGCAGTGAT[C/T]CAATCTATCGTTGGA | 10533 |
| rs553863328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359575 | GTGATGCACACCCGT[A/G]CTCCCAGCTACTCAG | 10533 |
| rs553866444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439194 | CTGCCTCAGCCTCCC[A/G]AGTAGCAGGGACTAC | 10533 |
| rs553882197 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ATG7 | GRCh38.p7 | 3:11471278 | GCTGGCCCTGGCGCT[C/T]TGGACTCCTCACACT | 10533 |
| rs553898498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458130 | TCTGTTTTGCTACAA[C/G]AAAACATTTCAAGAG | 10533 |
| rs553900745 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11352357 | TTTATAATTCTTTGG[A/G]TATATACCCAGTAAT | 10533 |
| rs553937308 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11345424 | AAAAATAAAATAAAA[G/T]AATTTTGTTGGTTGG | 10533 |
| rs553944184 | snp | C/T | 0.000430237 | 0.0146606 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554877 | CTGACTTCTCCCCGG[C/T]CGCCTGCTGAGGAGC | 10533 |
| rs553944261 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496480 | CCTACCATAGCACAA[A/G]CTGTAATACCAAGTT | 10533 |
| rs553959728 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479712 | AATGGAGGAGCTTTA[G/T]CAAAAGAAAAGGGAG | 10533 |
| rs553969882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551346 | CCGGCTCCAGAAAAC[A/G]TTTGTTAACTTTGAA | 10533 |
| rs553974087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11338953 | GTTTCCCAAGGAAAG[A/G]AAAATTGTGATCTTG | 10533 |
| rs553976770 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379907 | TTGTCAGAAACCAGA[C/G/T]GTGCATTTCATAGAT | 10533 |
| rs553983478 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11372821 | GTGTGTGTGTGCGCG[C/T]GTGTGCGTGTGTGTG | 10533 |
| rs553992891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405367 | TATGGAGCTTGAGGG[C/G]GTGAGGCGATGAGAA | 10533 |
| rs553994231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549639 | TTTCTCTGCTTTCCC[A/G]TTGATGATCATTTGT | 10533 |
| rs553998773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11279553 | GCCAGGCATGGTGGC[A/G]GGTGCCTGTAATCCC | 10533 |
| rs554000448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330300 | ATTTGCTTATATAGT[C/T]TGGAAATTTTCTTTA | 10533 |
| rs554007428 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11366142 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGGTT | 10533 |
| rs554029382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378991 | AGTGTTGAAGACAAA[C/T]GCTGTGGTATTCTGA | 10533 |
| rs554031175 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11276806 | CTGCCCTCTACTATA[G/T]TCTTTTCAACCGCAG | 10533 |
| rs554059449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472049 | GCCTTTTTCAGATAA[G/T]TTCTTCAAGATTAAA | 10533 |
| rs554068139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11389370 | TATGAACTTAATCAT[A/G]GTTTTCTAGAGTGTC | 10533 |
| rs554071318 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11433218 | AGCCCAGGAGTTTGC[A/G]GCAGACAGTGAGCTA | 10533 |
| rs554073975 | in-del | -/TAAG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11435781 | TCACAATTACCATAT[-/TAAG]TAAGAAGGCACCTTA | 10533 |
| rs554076056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543472 | GGGCAATGGTTCCCT[A/G]AGAAGAGGGGTTTGG | 10533 |
| rs554076487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449802 | GTACTTGGAAAAATA[C/T]ATATTAGTTGAATGA | 10533 |
| rs554081826 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556382 | GTGCACCAGGGACCC[A/G]GCCGCCAGCACCGCC | 10533 |
| rs554086584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304285 | CAACACAGATCTGGG[C/G]TGTACTATTTGCTCA | 10533 |
| rs554089414 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500158 | ATTCAATAGCAGCAA[C/T]GCGCAACATAAAGAA | 10533 |
| rs554099293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464262 | CTGAAGTCCCAGCTA[C/T]TTGGGAGTCTGAGGT | 10533 |
| rs554099874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472700 | CAGGTGGCTTGTGTC[A/G]TCCTTTTTTGGTAAA | 10533 |
| rs554106272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449588 | GAGAATGATTTTCCC[A/G]ACCCTTCCCTTGGGT | 10533 |
| rs554121212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11351888 | TTAAGTTCTAGGGTA[C/T]ATGTGCACAACATGC | 10533 |
| rs554129491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526116 | TCATCAAGGGCCAGG[C/G]ACCATGGTTCATGCC | 10533 |
| rs554131837 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11531708 | AAACCCTGTCTTTGC[-/A]AAAAAATTAGCCAGG | 10533 |
| rs554148019 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530449 | TTCATCAGTTTTGAG[A/G]AACTTGGATGCTGAA | 10533 |
| rs554156818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304784 | ATACGCATTATCGCA[A/C]GTTCACTATTGGCCT | 10533 |
| rs554167553 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11443327 | CTTACTACTAAGGCT[G/T]AGGGGCAAAGGAGAT | 10533 |
| rs554169278 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533012 | TCACAGACAGGGTGG[A/C]GAGGAGAAGCAAGCC | 10533 |
| rs554171284 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11388432 | TGCTCATGTTCCTTC[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs554172389 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382620 | TATGAGTTGCTCTTT[A/C]CTTCTACAAAGAAAT | 10533 |
| rs554181653 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11343417 | TTATTTCTTTTGTGA[A/G]TTTTATTTCTTTTAT | 10533 |
| rs554195001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11404806 | AGGGGAACTCCCTTT[A/G]TAAAACCATCAGATC | 10533 |
| rs554212433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541142 | CCTGACTTCGTGATC[C/T]GCCCGCCTCGGCCTC | 10533 |
| rs554233681 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372505 | AATGAACCCATTTTA[A/G]TATGATTTGACAAGT | 10533 |
| rs554248194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484496 | ATCCATAATTTAGGA[A/C]AAAATTGGCACATCT | 10533 |
| rs554259096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529363 | AGCTGCTTGCCCCTC[C/T]TACCACAAGCAGTAA | 10533 |
| rs554268959 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11489629 | AGTGCTATAAATTTC[C/T]CTCTACACACTGCTT | 10533 |
| rs554274000 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11413318 | TTGCATATGGCTTTT[A/G]TTATGTTGAGGCAGT | 10533 |
| rs554306383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11486308 | CTTTGAAGCAATTGT[A/G]AATGGGAGTTCACTC | 10533 |
| rs554313858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398634 | AAGGCAGGAGGATGG[C/G]TTGAAGCCAAGAGTT | 10533 |
| rs554316258 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306979 | TTGCTGCCCAGCTAT[C/T]GGAACACTGTATAAC | 10533 |
| rs554320739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407443 | TGTCAGTGGATCTAT[C/T]ATTCTGAGGTCTAGA | 10533 |
| rs554337155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341140 | AATCTCTGCTCACTG[C/T]AACCTCTGCCTCCTG | 10533 |
| rs554356896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513681 | TTGGCCAGCCCAGAA[A/G]GGGGCTCCCACAGTG | 10533 |
| rs554356940 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314436 | TTGTTCGTACAAATC[C/T]GAGGTTGTGGTTTTG | 10533 |
| rs554359273 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11318265 | CTCAGCACACGTGAT[G/T]AACACCTCCTTATGG | 10533 |
| rs554363793 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11319779 | TACCACCCCTGTGTC[-/T]TGTGGATTTCATGTC | 10533 |
| rs554366818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387262 | AGAAACCTTCCGTTC[A/G]TGTCTCTTGACAATG | 10533 |
| rs554368129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475923 | CCCCCTCCCAGAGTC[C/T]GAGCATTCTAGAGTT | 10533 |
| rs554368962 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297816 | GCATTTCTGAGTGGC[A/T]GGATTTAGGATTTTG | 10533 |
| rs554374669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332022 | GCTCAGCAATGTTAC[C/T]CTCAAGTATATTACT | 10533 |
| rs554379781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313643 | GTCTCACCCCCATTA[C/T]GCAGGCTGGAGTGCA | 10533 |
| rs554383064 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11439020 | GTAAAATTAAATTGA[-/T]TTTTAGTTCTGAGCT | 10533 |
| rs554400497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348319 | GCCGCGGACCTTCGC[A/G]GTGAGTGTTACAGCT | 10533 |
| rs554414405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11362238 | TTTGGTTGAACCAGC[A/G]AAGGCTTGTGCTTAG | 10533 |
| rs554429530 | in-del | -/TT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11525468 | TTTTTTTTTTTTTTT[-/TT]ACTCCTTTGCCCTTG | 10533 |
| rs554444766 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11281160 | CCATATTGGCCTCTT[C/G]TGATTACTTAGGGCT | 10533 |
| rs554446636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508922 | TTAATAACAAATTAG[A/C]TCTCTGCTCCTGTTA | 10533 |
| rs554456681 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304878 | ATACCATAAAATTCA[A/C]CCCTTAGTTTAAAGG | 10533 |
| rs554459039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484833 | TTTACTGAGAATGAT[A/G]ATTTCCAATTTCATC | 10533 |
| rs554463820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429334 | AACCCCGTCTCTACT[A/G]AAAATGCAAAAATTA | 10533 |
| rs554468393 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11444010 | TGTACAACTTCAGTC[G/T]GGTATATGGGTCTTA | 10533 |
| rs554472751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305567 | TTTGCCTTCCCTCTG[G/T]GCTTAATCTTTTCCC | 10533 |
| rs554485055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432615 | AACTTATCTACATAA[C/G]CAAAAATCACCTGTA | 10533 |
| rs554511343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371312 | GCTGGGAAAGGTGCT[C/T]AGCGAGTTTGAGGAA | 10533 |
| rs554518422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513251 | CGTGCGTCTGCACTC[C/T]TCAGCCCTTGGGTGG | 10533 |
| rs554518634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481661 | GGACTTAATGTCAGC[A/G]CCACCACAGTGCCAA | 10533 |
| rs554524631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393768 | TCACTGCAACCTCCA[C/T]CTCCAAGGTTCAAGG | 10533 |
| rs554530817 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11423693 | GCTTGACTCTACGCA[C/T]GTAATGGTCCTACAC | 10533 |
| rs554533835 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11363120 | GTTTCCTTTGTGGCC[A/G]CATTTCTGCATCTTT | 10533 |
| rs554535640 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271547 | TTTCTAATAAGTATC[C/G]TTATTAGTCTGGATT | 10533 |
| rs554539605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343549 | CTAAGGTGTCTTTAG[C/T]CATATAAAAGTTTTT | 10533 |
| rs554569014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355393 | TTAGTTGACTTTATA[A/G]AAATTTAAAACTTCT | 10533 |
| rs554579654 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359357 | GATATTTGGGATAAT[A/G]AGTTAAATTAGAACT | 10533 |
| rs554605433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415229 | ATTTTTTTAAAATGG[C/T]ACACCTGTGCAGAAT | 10533 |
| rs554615197 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374797 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10533 |
| rs554620538 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270614 | GGATTATCATTGGTT[C/G]TTATAGGTTTTGGGA | 10533 |
| rs554625905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461416 | TGCTTAGAATTTCCA[C/T]GGCGTCTTTTCTTCC | 10533 |
| rs554626823 | snp | A/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450380 | TTTTCATGTTCTCCA[A/G]ACCTCAGTTCTCTAG | 10533 |
| rs554635067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401857 | TCAGCAGGATTAATA[A/G]CTGTTTAACCTACGG | 10533 |
| rs554638385 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499038 | AGAAAAAACAGTCCA[C/T]AGCAGTTCCATTTAT | 10533 |
| rs554652181 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376868 | CTCAGCCTCCCGAGT[A/C]GCTGGGACTACAGGT | 10533 |
| rs554655004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498872 | CCGATCCTAGGAGAG[C/T]GTATGAGCCAAACTG | 10533 |
| rs554666886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11407845 | ACCCTGGGCTCAGCC[C/T]TTGAAACCATTTTTT | 10533 |
| rs554668839 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11307430 | TGTGCCTTGGAGAGG[C/T]TTGGCAATCCTGTGC | 10533 |
| rs554670027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498105 | AATCCTGACTCTCAA[A/T]CCAGTATTCTTCCTC | 10533 |
| rs554670223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491992 | TGGTGGGCTACACCA[A/G]GTTTGAGCTTCCCGG | 10533 |
| rs554677360 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11309518 | TCTAATTAAAATGAA[C/T]GTTAAGGGCAGCCTT | 10533 |
| rs554687324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455270 | TTAACTACAGTAGTA[A/G]AGTCCTAAAATTTCT | 10533 |
| rs554700808 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11497043 | TTAGTAGAGACGGGG[-/T]TTTCACCGTGTTGGC | 10533 |
| rs554721276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401218 | GGGATTCTGAAGCAT[G/T]CTCAAGTTTTGATAA | 10533 |
| rs554721448 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG7 | GRCh38.p7 | 3:11488542 | TGCCCCGGGCCGCAG[C/T]GCAGCGGCGCCAACC | 10533 |
| rs554745000 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530891 | GAGGCTGAGGCAACG[G/T]TGTTGCTTGCCCCTG | 10533 |
| rs554751731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370451 | CTCCATTTTGGCATT[A/G]AACTTGATTAAGACT | 10533 |
| rs554752561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429835 | CGCCTGTAGTCCCAG[C/T]TACTCTGGGATGAGG | 10533 |
| rs554758459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11405250 | AAAAATGAAGATTTA[C/T]AGAAGCTCTGACTCT | 10533 |
| rs554764212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292135 | ACCTAGACAGGAAGC[A/C]TGAAGTTGCATGAGG | 10533 |
| rs554764779 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456980 | CAACAATACACACTG[C/T]CCTCCTGCTGAACAG | 10533 |
| rs554767816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284907 | GCTGGAGTGCAGGTG[C/T]GCAATCTTGGCTCAC | 10533 |
| rs554782917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488769 | CACTTGATCATGGTG[A/G]ATAGGCTTTTTGATG | 10533 |
| rs554787170 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11397365 | TACTTTATAATAATT[A/C/G]GTTTTAATTCACCAG | 10533 |
| rs554790203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11505069 | GAGGTAACTAAAAGT[A/G]TCAGGTAAGTCTCTA | 10533 |
| rs554802747 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516667 | AACTTAGAAGCAACC[A/G/T]AGATGTCCTTCAGTA | 10533 |
| rs554805445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493084 | AAATTGTTGTCCAAT[C/G]CCAAAAAAGAATGAG | 10533 |
| rs554821490 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520258 | CCTCGATATGCTCCT[C/T]TACCATGAGTGGCAA | 10533 |
| rs554828522 | in-del | -/GTG | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447328 | AAAAATTAGCCTGGT[-/GTG]GTGGCAGGCATCTGT | 10533 |
| rs554839918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511492 | AGCTAGATATAAAGA[C/T]TCTCCATGTCCCCAC | 10533 |
| rs554867186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482205 | GTTCTGTGAGAAGGG[C/G]AATGGCTCTCCCTGA | 10533 |
| rs554888455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438365 | AAGTCAAACAGGAGT[A/C]AAACATTTAGGACTT | 10533 |
| rs554888491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396015 | AGGTATTTTGTATAG[A/C]CAAGAACAGAGTCCA | 10533 |
| rs554891775 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11384699 | GCATGGTGGCTCACA[-/C]CTGTAATCCCAGCAC | 10533 |
| rs554943983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329321 | GCATTGTGGGAAATA[A/T]AAGGGAGTGTTTAGG | 10533 |
| rs554950026 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11499520 | GGAGGCCGAGGAGGG[C/T]GGATCACCTGAGGTC | 10533 |
| rs554952139 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11505480 | TGGTTATTGTTTTAA[C/T]ATAACATTATTCTTT | 10533 |
| rs554980723 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315109 | GGAACTACCATGTTG[C/T]AGTCCCTTTGTGCCC | 10533 |
| rs554981410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542306 | ATCCCCAGAGGGAGG[A/G]TGCCAAATATAGCGG | 10533 |
| rs554981459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416108 | TGTATCATTGGATTC[A/G]ATTTGCTAATATTTT | 10533 |
| rs555004846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335634 | TCCACTTTTATGACA[A/C]AGTCACTGAGTTATT | 10533 |
| rs555009315 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385653 | CCAATACCAATTAAT[A/T]TTGTAAATGTGGAGG | 10533 |
| rs555022143 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481146 | TTGTGCAGAGCACTG[G/T]GTAAGCACCTACTGT | 10533 |
| rs555022353 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11508889 | AACGTGATCTGCACT[G/T]ACAAAACTAATAACA | 10533 |
| rs555036863 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11466005 | ACAGAGGGCAGTAAA[A/T]TTTAGCTCTAATTAT | 10533 |
| rs555046630 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11388033 | TGAAACATCTCTGTG[C/G]ATCCTAGTAAAGCAC | 10533 |
| rs555053270 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472604 | CAAGCAGAGCAACAG[A/G/T]TGTCCACTGTGGTTA | 10533 |
| rs555067078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422788 | GACAGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA | 10533 |
| rs555068302 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11516208 | ATGAAAAGATGTTCC[A/G]ATAGCATTAGGAGAT | 10533 |
| rs555081219 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555520 | CCTGCTTGAGGGAGA[A/G]GAGTTTCTGCTGCTG | 10533 |
| rs555091186 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11548239 | AGATGGGGTCTCACT[A/C/G]TGTTGCCCAGGCTGG | 10533 |
| rs555097667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293061 | GCAAACTAGGAAATA[A/C]AGAGAAAGGGGCAGA | 10533 |
| rs555100586 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326500 | AGATGGGGTTTCACT[C/G]TGTTAGCCAGGATGG | 10533 |
| rs555112639 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392687 | ATATCAGCTTGATCA[C/G]AATCATAATATTCCG | 10533 |
| rs555112661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11347508 | TTATACTTAATTATT[A/C]GTTAAGGGAAATCAA | 10533 |
| rs555115350 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11502278 | GTGCACATTGTGCAG[A/G]TTAGTTACATACGTA | 10533 |
| rs555122695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491025 | TGTTGGCCTACCTTG[C/G]TAGATTGGGGAATTT | 10533 |
| rs555159611 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11484186 | ATCACTGGAGGCCAG[A/G]AATTCGAGACCAGCC | 10533 |
| rs555161036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444578 | GCCTCTTCTGGACCA[C/T]GGACTTAAATGTAAA | 10533 |
| rs555161444 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372710 | AGGGAAAAAAAATGT[A/C/G]ATGGAAATCTTAAAA | 10533 |
| rs555162193 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556183 | CCACAGAGAATGGTA[C/T]ATTACAGATTTACAC | 10533 |
| rs555167704 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467722 | TGTGGGACTTATCAC[C/T]GTTTGGCATTATTAT | 10533 |
| rs555168215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386667 | ATATAAATCTCTGAT[G/T]TGGAAAATGATGAGT | 10533 |
| rs555184043 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11491455 | GTTTGATCGTCAGAA[A/G]CCTTCTTCTCTCAAC | 10533 |
| rs555196508 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11474472 | GGGCATGGTGGTGTG[C/T]GCCTGTGGTCCCAGC | 10533 |
| rs555200488 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11275232 | AACAAAATTCTTTGA[C/G]TAGTGTCTCTAATAG | 10533 |
| rs555201143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11551329 | GCCTAGAACCAGCTC[A/G]CCCGGCTCCAGAAAA | 10533 |
| rs555208629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495754 | AAGTTTCTATTTTGC[C/T]GTGTTTCATAAATGT | 10533 |
| rs555221647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456738 | CAAAAATGTGACGGA[A/C]AGAAGTAGACACTTG | 10533 |
| rs555226412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445113 | TTGGTGGAAGTGTAA[A/G]TTAGTTAAATCGTTG | 10533 |
| rs555262954 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11281511 | GGTGTGGTGGCTCAC[G/T]CCTATAATCCCAGTA | 10533 |
| rs555267453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537058 | CCCTCTGATGGCAGA[C/T]CTCCATCCCTCTGCA | 10533 |
| rs555273301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323272 | AAGTCCTGGAATGCC[A/G]AATTGAAAAGAGACA | 10533 |
| rs555273544 | snp | A/G | 0.000365509 | 0.0135137 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11315389 | CTTTGTCAAACAGAA[A/G]GAGTCACAGCTCTTC | 10533 |
| rs555308179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537518 | GATGGAGACTTCCTT[A/C]ATAGAGCCCCATTTT | 10533 |
| rs555323985 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG7 | GRCh38.p7 | 3:11418967 | ATGGGAAACTGCCCC[C/T]CCCCCCCGATCCAGT | 10533 |
| rs555324952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413019 | ATAGAAACGTAACTG[G/T]TTTTTATGTTAACTT | 10533 |
| rs555338069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11514691 | CTGATATGCATAGCA[C/T]ACTTACATAGCTCCA | 10533 |
| rs555343852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427757 | GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATTGTG | 10533 |
| rs555350671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11367828 | AGCAGGCAGCAGTAA[C/G]TATAAGCTAATTTCT | 10533 |
| rs555377282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332676 | TTGTGAGCATTTTTT[C/G]CGCATTTAAAAGATT | 10533 |
| rs555378804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515265 | TCAACTGAGAGGTGG[G/T]GTCGGTGTTTCTACT | 10533 |
| rs555380455 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318805 | ATCTCTCTGCCTGCA[C/G]ACATCTCTCTGTCTC | 10533 |
| rs555383749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426350 | GAAGTACCTATTGAA[A/G]TTTATTTTTCCATTT | 10533 |
| rs555420813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544600 | GCTGCTCCCGCCTGG[G/T]GATGCTCACAGTGCT | 10533 |
| rs555431670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400518 | GAATAACGTTGCCAT[A/G]TTTTCTGATTTTTTT | 10533 |
| rs555433119 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325575 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATTGCTTG | 10533 |
| rs555440949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419743 | ATATAGTAAAGAGTA[A/G]GGAGTCACCAAAGTG | 10533 |
| rs555444813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287957 | GCCTGTGGATCAAGT[A/C]CTGCCCGAGGCCTTT | 10533 |
| rs555444992 | in-del | -/CT | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11496942 | TCGGCTCACTGCAAC[-/CT]CTGTTTCAAGTGATT | 10533 |
| rs555462522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508276 | GCTTCCCTGAGCCAC[C/G]TTGGAAGAATAATTA | 10533 |
| rs555463095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297958 | GAAGCATAAACATTA[A/G]GGCCGCAAAGGTTAC | 10533 |
| rs555465541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425834 | CTGTGGGTAGCCACT[A/G]TCTTTTCTCCTAACA | 10533 |
| rs555468010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434781 | GATGGTATAATCCGC[C/T]TGGAGAAGTCTAAGC | 10533 |
| rs555485877 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499602 | AATACAAAAAATTAG[A/C]CAGGTGTGGTGGTGC | 10533 |
| rs555493238 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300389 | GGCCAAATTTAGAAA[A/G]CAGGGGTGAGAGAAA | 10533 |
| rs555496239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296811 | CCCATCCTTTTCAAC[A/G]TCACTCAGTGCCCAT | 10533 |
| rs555503806 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551412 | GCTGACATCTTTATG[A/G]ATGTTGAATCGTCCT | 10533 |
| rs555521025 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11421082 | TTTTTTGCTAAAAAA[C/T]GCTAACAATATTGAG | 10533 |
| rs555522085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527168 | GGAGTACAGTAGCAC[A/G]CTCTCGGCTCACTGC | 10533 |
| rs555537103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327344 | ATATTTATGCAGTGA[A/G]CCCTCTTTTAAGCAA | 10533 |
| rs555539952 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11443942 | CATCTCATATTTTAC[-/T]TTCTGACCACAGGCC | 10533 |
| rs555550649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441521 | TGCTGGGATTACAGG[A/C]GTGAGTCACCGCAAC | 10533 |
| rs555560041 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11414632 | GTTCCTGTTTTCTTG[-/C]CTTCTTGCCTTCATG | 10533 |
| rs555561888 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468085 | TGTGACATCAGAAGG[C/T]TGACAGGCAGAAGTC | 10533 |
| rs555563036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453587 | TCAGTGATGTTCCAA[A/G]CTCTTTGTCTTCTAT | 10533 |
| rs555564835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406776 | TCTTAAAACCATCAG[A/C]TCTCATAAGACCCAT | 10533 |
| rs555588636 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306714 | GGACAGTAGAACAGC[A/G]TCCTGATAGGTTAGA | 10533 |
| rs555598770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480383 | CTCTACAAAAACATT[A/T]AAGATTGGCTGGGCG | 10533 |
| rs555605353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442009 | GGTTTCACTATGTTG[C/G]CCAGGCTGGTCTTGA | 10533 |
| rs555622791 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11465716 | GCTGCAGTGAGCAGT[A/G]ATTGCACCACTGCAC | 10533 |
| rs555644062 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11460764 | ACAGTGAGATAATGA[A/T]TATTCTTATAAAGTA | 10533 |
| rs555652515 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11329408 | GTGTTTTCATTTAAC[A/C]CATGCTATGCTTATG | 10533 |
| rs555675448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11326270 | CCTTTTTACACTTGA[C/T]AGAGTTGTAAATGCT | 10533 |
| rs555684574 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496719 | GAGTAAAGAATTGAG[A/G]GTGTTTTATGGGCTA | 10533 |
| rs555713039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304780 | TAGTATACGCATTAT[C/T]GCAAGTTCACTATTG | 10533 |
| rs555732932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11435675 | GTGTCAGGCAGGACC[A/G]TGTGCAGCAGTCATG | 10533 |
| rs555734060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517401 | ACAGTAAGATCACTG[A/G]TTCAGGTTAAGGGAG | 10533 |
| rs555734115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11330190 | TGCCAGGTTTCTCCA[C/T]TGTAAAAATACTATT | 10533 |
| rs555739882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524457 | AAGAATGTATAGTCT[A/G]TTTTTTATGCTTTAA | 10533 |
| rs555741580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552406 | TTCACTAAGAGGACA[C/T]TCACTGTGCCCCTTC | 10533 |
| rs555743512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333455 | TTTATTTGTTATATA[C/G]TTAAAGTTGTATGTG | 10533 |
| rs555748716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453165 | GTTCAATGTTGAGGG[A/G]GCTGAGAGTTCTCTG | 10533 |
| rs555749992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283330 | TTGTTGGCTAATATG[A/G]GGCAGTGACAAGAAA | 10533 |
| rs555772809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517957 | GGATGGATTGGGGTG[A/G]TCAGGCTGGCTCAAG | 10533 |
| rs555777917 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309662 | ATAGAGATACCAGCT[A/C]TGCATGCATGCGCGT | 10533 |
| rs555783349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392567 | TTTGGCAGGCACCCA[A/G]GCCCAGCAAAACCCA | 10533 |
| rs555784558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381703 | TTACATAAACATGTT[G/T]GACGATTTAATACAA | 10533 |
| rs555812520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312544 | CTCCATGGCTCTAAT[C/T]ATGCACTCGCTTTAT | 10533 |
| rs555813856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357411 | TTTTGGACAGAGAGT[A/G]AAGCCTTACTCTGTC | 10533 |
| rs555814860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11393935 | GTCCTCCTCCCTTGG[C/T]CTCCCAAAGTGCTGG | 10533 |
| rs555816346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11435724 | ACTTCATTGACCTTC[A/G]TTTCCATCATTTTGT | 10533 |
| rs555817060 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11351623 | TCCTTCACACTTACA[C/T]TGTGTTACTCTGTTT | 10533 |
| rs555823779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308398 | TCTCTCAGGGCAAGA[A/T]AATCTCAAATAAGAC | 10533 |
| rs555844258 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369046 | TGGCCTGGGAAAACT[C/G]TAATTGAGTCACATG | 10533 |
| rs555852226 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326738 | GTCCCTGATGGAAGA[C/G]TAGCAGGTGGGGTGG | 10533 |
| rs555852537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523536 | TGATGGAAAAGTCTG[G/T]GCTGCCATTCCTCAG | 10533 |
| rs555853123 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11424486 | TGTCACCAACAACAA[A/C]AAAAAAAACACTGAT | 10533 |
| rs555856763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308920 | TCAGCTCCACACTTC[A/G]CCTGAGAGTGAGAAA | 10533 |
| rs555860557 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11301629 | ACTGCTTGTGGTTAC[C/T]TGTCAAAAGAAATAA | 10533 |
| rs555865914 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284118 | TTTTTTTCTCTCCCT[C/G]TGTTTTTTATTTTCT | 10533 |
| rs555868391 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11446370 | CCCTGAATTAAGTAT[G/T]CCAGAGACTCTTTAT | 10533 |
| rs555872230 | in-del | -/TTC | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11424816 | TGTACATCCATGCAT[-/TTC]TTCTTCTTCCTGTCT | 10533 |
| rs555886525 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430882 | TTTAAAGGATGAGTA[A/G]ACTATTTTTAAAAAT | 10533 |
| rs555892193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554416 | GCCAGAATTCCTGCC[C/T]TCAGGGAGCTTGCCT | 10533 |
| rs555892233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438827 | TCTCTGGCCTGTGGC[A/G]CTGCTGAGCCTAACT | 10533 |
| rs555918863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511732 | GCTGCAGGTCCTGAG[C/T]CCTGCCCCGAGGGAA | 10533 |
| rs555919000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11300672 | AACTTATGGTGGTTT[A/G]ATGACTTTTTGACTT | 10533 |
| rs555927264 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11329810 | AGAATTCTTACATTA[C/G]TATTAACTCAGCTCT | 10533 |
| rs555929774 | snp | A/T | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526480 | TGACTATTTTTTAAG[A/T]TGCTAATTTATAAGC | 10533 |
| rs555930754 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557083 | CTGGTCAGGTGCCAT[C/G]GTCGTGAGCCTCTGG | 10533 |
| rs555939031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353604 | GGAGGTGGATCCCTC[A/G]TGAATGGCTTGGTGC | 10533 |
| rs555939177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542990 | TCTGGAGGTGGCATG[C/T]CAGCCCACACGTGTG | 10533 |
| rs555940124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329903 | TACTACATTGCAATT[C/T]GTTGTCATGTCTCCT | 10533 |
| rs555940990 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11345758 | TTCGTAAATATCTAC[A/T]TTTATCTTTATTAAT | 10533 |
| rs555956104 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11336234 | GAGACGGGGTTTCAC[C/T]GTGTACCCAGGCTGG | 10533 |
| rs555960655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542989 | CTCTGGAGGTGGCAT[G/T]CCAGCCCACACGTGT | 10533 |
| rs555977279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330279 | TTTGCTTCTGAAGAG[A/G]CCAGTATTTGCTTAT | 10533 |
| rs556004461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370163 | ATCTTTCACTTTTAA[C/T]TAAAATGGAAACTTA | 10533 |
| rs556015717 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11363939 | TGTCTTCCTCTTTGT[C/T]ATCCACCTTAGCTAT | 10533 |
| rs556025629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388762 | TCATATAGTACATTC[A/G]TCTTCATCCTCTTGC | 10533 |
| rs556025987 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533343 | ATGGTAAACCTCCTC[G/T]GGGGTGATTTTTTTT | 10533 |
| rs556026055 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11482838 | ATACAATTAAGTGCA[C/T]ATATCTTAAGTATAC | 10533 |
| rs556026843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276123 | TCTCTTGTCCATTTC[C/G]CTTTATGTCTTCCTC | 10533 |
| rs556060768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382289 | ACACATATATATAGA[G/T]AGAGAGAGTGCGAGC | 10533 |
| rs556061533 | in-del | -/TCAGATT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395447 | CAAGACCCATCATAA[-/TCAGATT]TCAAACTTCAGAAAA | 10533 |
| rs556082371 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11336613 | CTTTTCAATACTTCT[A/G]AGACATCCCATAGTT | 10533 |
| rs556083778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466900 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACCTGA | 10533 |
| rs556098366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467304 | GAAGTCTTTGAACAA[C/G]TCACCTAACCTGTTG | 10533 |
| rs556107270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11358281 | GAGAGGGCGTGGGAA[A/G]GGTGCAGCATAATAG | 10533 |
| rs556131295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507246 | AAGATCACACCACTG[C/T]ACTCCAGCCTGGGAG | 10533 |
| rs556142225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358851 | CTCTACACTGAAAGA[C/T]ATACTGTACTTACAT | 10533 |
| rs556145572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11343126 | TAGAGACGGGGTTTC[A/G]TCATGTTGTCCAGGC | 10533 |
| rs556160286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391709 | TGGTTTAATCTTTTC[A/C]AGTGCTACAGCATTT | 10533 |
| rs556169271 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280197 | GATTACAGGCGCCTG[C/T]CACCATGCCCGGCCC | 10533 |
| rs556173817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350001 | CATTTTATCTGACAG[C/G]AGTTAGATTAGGTGT | 10533 |
| rs556181683 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11488506 | GCGGGTGTCAGCGCC[A/G]CGACTGTCCCGGCTC | 10533 |
| rs556197370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543434 | TCAGCCCTCAGCTGC[C/G]TGTGTCTGGAGAGCT | 10533 |
| rs556197465 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420816 | GCTGGAGTGCAATGG[C/T]GCGATCTCGGCTCAC | 10533 |
| rs556197607 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11449395 | AACAACAAAAAACCC[C/T]GAGATTTGGGGCCTG | 10533 |
| rs556198083 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391644 | ATCTTGCTTTTTCTA[C/T]CGCAGCTATAAATGG | 10533 |
| rs556200505 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11521973 | TCAACTCTTTATGCC[A/G]TTGGTCCTCACTGCA | 10533 |
| rs556208703 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11396034 | GAACAGAGTCCACCA[C/T]TAGCATGTTTACACA | 10533 |
| rs556215161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295272 | TGAAGCTTATCAATT[A/G]TATAGAAAAATAATT | 10533 |
| rs556223909 | in-del | -/A | 0.00240096 | 0.0345646 | intron-variant | ATG7 | GRCh38.p7 | 3:11372445 | TTAAGATTATAAGCC[-/A]TTTTTTAAAATCACC | 10533 |
| rs556244970 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11389731 | TCATTGGAATATATG[C/T]GCAGCCTCCCACGAG | 10533 |
| rs556253558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11444492 | TCCTTTGGGGGTGAT[A/G]TCACCCTCTTTGTGA | 10533 |
| rs556264000 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11521268 | GAACGCTGGCCATAC[A/G]TGCTAGATGCTGACA | 10533 |
| rs556268969 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11380264 | AATGTGTAGGGAGAC[G/T]GAGTTAAAATATTTC | 10533 |
| rs556270397 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368109 | TGATTTTGAACTTCT[C/G]TAAATGAAATCATAT | 10533 |
| rs556282195 | snp | C/G | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270661 | AAGCAATGTTTTGGG[C/G]GTAGGGGGTGGATCT | 10533 |
| rs556285354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11538101 | CCCCAGGGCTGACAG[A/G]TGTTCCTGAGGGCCA | 10533 |
| rs556314568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483077 | ATTTAATATGTAAGA[A/G]TGCAAAATTATCAGC | 10533 |
| rs556332966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357391 | GGTTGATGGACAGCT[C/T]CTACTTTTGGACAGA | 10533 |
| rs556334934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349170 | AGCTAGACACACAGC[G/T]CTGATTGGTGCGTTT | 10533 |
| rs556346932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378889 | GGATTTGAGGGAGAG[A/G]GCATGGTGTTAATAG | 10533 |
| rs556367228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478889 | TAAGTATTTATGTAT[A/G]TAATTGAGATATTTA | 10533 |
| rs556370502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464774 | GTTCTGGAGTCTGAC[A/C]CCCTATTTTCAAATT | 10533 |
| rs556379794 | in-del | -/AAT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11332943 | TAAAAAAAAATAATA[-/AAT]AAATAAAAATCCGGG | 10533 |
| rs556380874 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410303 | TACCTAGGTATTTTT[A/G]GGTGTTGCTAATGTG | 10533 |
| rs556384405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336235 | AGACGGGGTTTCACC[A/G]TGTACCCAGGCTGGT | 10533 |
| rs556387535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279465 | CCGAGGCGGGTGGAT[C/T]ACAAGGTCAGGAGTT | 10533 |
| rs556395073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411242 | CCATTTGTATATCTT[C/T]AGAGAAATGTCTGTT | 10533 |
| rs556429367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457946 | GTAACCGGTAAGTAT[A/T]TATTGGTTGAATGAA | 10533 |
| rs556435788 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553324 | GAGGAGTGAAAGAGG[A/G]AGTATTCGCAGCAGG | 10533 |
| rs556439854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11511856 | GCTAAGTCCCCCACT[A/G]CCTGGGGCCAGCAGG | 10533 |
| rs556441371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11393093 | TGATGGAATCCTCTG[C/T]TAAGTGTCCAGACCC | 10533 |
| rs556441856 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304045 | GCAGTGAGCCGAGAT[C/T]GCACGACTGCACTCC | 10533 |
| rs556442761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500315 | GCTGTTTAGTTAATA[A/T]GATATTAATGTATTA | 10533 |
| rs556453970 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469970 | CTCCAGCCTGGGTGA[C/T]GGAACGAGACTCCAT | 10533 |
| rs556456362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478282 | GAATGAATCTCTATC[C/T]CTCTTTTAGAAACAT | 10533 |
| rs556466850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446453 | CTTAATTTAGTCCGT[A/G]GGGGAAACTTGGCGT | 10533 |
| rs556472584 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530249 | GCTCCCAGAGAGAGC[A/G]AGGCCCTGCAAGCAG | 10533 |
| rs556473503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384328 | GGTTTGCATACCATC[C/T]GGGACCTGCGCAGAT | 10533 |
| rs556485593 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306140 | GGCCTTTGGGGGCAA[C/T]GTAGAGTGTGTAAAC | 10533 |
| rs556495663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477541 | GCAAAAGATAAGGGC[A/G]TTTGTTAGACACAGC | 10533 |
| rs556498405 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475235 | ATCTCTTGAATACCT[A/G]CTGTGTTCCAGTCAT | 10533 |
| rs556502298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344784 | TGAGGTGGAAGGATT[A/G]CCTCAGACCAGGAGG | 10533 |
| rs556503296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361636 | TTCAAGACCCACTTA[C/T]ACTAAAAATTTATTT | 10533 |
| rs556522536 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11295829 | TTCGCTCTTGTTGCC[C/G]AGGCTGGAGTGCAAT | 10533 |
| rs556535196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490236 | CAATTATGTAATGGC[C/T]TTGTCTCTTTTGATC | 10533 |
| rs556535856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445905 | CTGATGATGTTAAAC[A/G]TCTTATGTATATTAC | 10533 |
| rs556540158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362196 | AACAACCTCTTAATT[C/T]GCCCAGAGTTGGATG | 10533 |
| rs556563674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310407 | ACCGTTCCTCCTAGA[A/T]TCCTAGATGCAGGGG | 10533 |
| rs556564339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11489509 | TTAGTTATTTCTTGC[C/T]TTCTGCTGGCTTTTG | 10533 |
| rs556566108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309876 | TTTCTAATATTCACT[C/G]TTATAAAAAATGCTA | 10533 |
| rs556567522 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379515 | AGGGCCATTTCGGCC[C/T]TCCACAGTCCCCCAA | 10533 |
| rs556577703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494244 | TACATGCAGGAAAAC[A/G]GGAATTAGGGAGGGG | 10533 |
| rs556592167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373992 | TAATTTATTGTCTTA[C/T]GAGCAAATCACTGTG | 10533 |
| rs556596368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484421 | AAACAAACAAAAAAA[A/C]CACAAAAACGACAAA | 10533 |
| rs556599445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546130 | GACAGAGTGAGGCCC[C/T]GTCTCAAAAAGTAAA | 10533 |
| rs556610901 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11499714 | ATCATGCCATTGCAC[G/T]CCAGACTGGACAACA | 10533 |
| rs556611556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11372207 | AGCCAAGAAACCACA[A/G]GTAATTGGGATTCTT | 10533 |
| rs556639470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327902 | GCATTTCTGAAGGCT[C/T]CCAGGGAAGGCTGAT | 10533 |
| rs556646147 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11365911 | CCCCAGCCCCCTTGC[A/C/G]CAAAACCACCCATAA | 10533 |
| rs556654600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11272720 | TCTTGGTAGGCAGTG[C/G]TCAGAATCTTCAGTG | 10533 |
| rs556663962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335854 | AGTCGCGTGCCACCA[C/T]GCCTTGCTAAGTTTT | 10533 |
| rs556666625 | in-del | -/TCACCTCACAGGTAGATGTGAGG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11553290 | CAGGTAGATGTGAGG[-/TCACCTCACAGGTAGATGTGAGG]AGTGAAAGAGGGAGT | 10533 |
| rs556676938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385694 | GCCTTGCAGAGGATG[A/C]CTTCTGAGTTGATGT | 10533 |
| rs556677293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500716 | TCTCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 10533 |
| rs556684223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460699 | ATCCCTGCCCCCTCC[C/T]AAATTTCATCCCAGT | 10533 |
| rs556686182 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433709 | CTTCCTTGCCTTGAC[C/G]ATATTGTCAGTATTT | 10533 |
| rs556701095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344247 | ATCTTCCTTTTCCTT[A/G]TCTTATAAGATTGGC | 10533 |
| rs556708574 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430295 | AAAAATGTGTGTATG[C/T]GCATATAAGCAAAAT | 10533 |
| rs556709673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403872 | ATTTCCCAAAGAAGC[A/G]TATAAACTAGAGCAG | 10533 |
| rs556715144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355232 | TGGAGTTCTGTATAC[A/G]GAGTGGAGAGACCTC | 10533 |
| rs556726603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491951 | AGAGGTGGAGCCTAC[A/C]GAGGCAGGTAGGCCT | 10533 |
| rs556746995 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11327316 | TACAGTCAGGAATTT[C/G]TTACAATTGTGTATA | 10533 |
| rs556755188 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11413596 | AAACTGACTTAATAA[A/G]TGAATTCAGCAAAGT | 10533 |
| rs556770630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484083 | GCAGCCTAAGAGGAA[A/G]GTGATAGGCCAAAAC | 10533 |
| rs556773989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374969 | AATGCTTGGGAGGCC[A/C]AGGTGGGAGGATCGC | 10533 |
| rs556786952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525512 | GCTCATTTGTTTGTT[A/G]ATTAACACCTTTTAC | 10533 |
| rs556790973 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371240 | TGTTTATTTGAAAGG[C/G]AAAAGGAAGAGAAGT | 10533 |
| rs556793942 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339741 | TCCCTTGAGATTGTA[A/G]TTGGTATACAGGGAA | 10533 |
| rs556795623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11519783 | ATCCAGGATAATCTC[A/G]ATCTCCTGACCTTGT | 10533 |
| rs556827000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11540536 | GTCCCAGCTACTCAG[C/G]AGGCTGAGGTGGGAG | 10533 |
| rs556832582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513214 | CCGGGGCTGCAGGTG[A/G]AGCTGCCTGCCAGTC | 10533 |
| rs556840905 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340214 | AAGGTTCAAATCCCA[A/G]TAGGAACCTCAGTGA | 10533 |
| rs556855523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347631 | AATAATTATTAGTCT[A/G]TTCCACTTGACATTT | 10533 |
| rs556878305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354510 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCACACCT | 10533 |
| rs556880289 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512868 | CATTTTACAGAGAGC[A/T]GATTGGTCCATTTTA | 10533 |
| rs556881767 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11398582 | GTACTTAATAAAAAT[A/G]TGGCTCATGCCTGTA | 10533 |
| rs556888583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376761 | TTTTATTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 10533 |
| rs556894760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504403 | CAAACCATTGGAGGA[C/T]GAACTCCAGAAAAGT | 10533 |
| rs556900465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340545 | TTGTCAATGCATGGG[A/C]CATTATGAATGTCGA | 10533 |
| rs556901691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11414355 | ACAGGCATGAGCCAC[C/T]GTGCCCAGCCTAGTC | 10533 |
| rs556908040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11518838 | TTATTTCTGAAAGTA[C/T]TGAATTCAACTGGTA | 10533 |
| rs556929878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277348 | TGGCATGGTCCATCT[A/C]CTCTGCCCCATGTGC | 10533 |
| rs556976343 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11395679 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10533 |
| rs556979723 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11431707 | TGTTGTAGCAAGGTA[C/T]GCAATTGTTTTTCAT | 10533 |
| rs556980554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11504979 | CGAGCAAAATGGGAA[A/G]TATATATAATGCCTA | 10533 |
| rs556983156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406955 | GTCCCTCTCAAATTT[C/T]GTATCTTCACATTTC | 10533 |
| rs557033920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475141 | TAGATTATATTGTTA[C/T]TGTTATTGACATCAT | 10533 |
| rs557035341 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11476741 | TCTTTTTCATTTTTT[A/T]CCAAAGCAAATGGTT | 10533 |
| rs557045564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461548 | TAAGATCACAGTGAA[C/T]TGAACAGACTCAAAA | 10533 |
| rs557048255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383026 | TCAATGTGAATTCCA[A/G]AGAACAAAGACATTC | 10533 |
| rs557049458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11375707 | TGGGATTACAGGCAT[A/G]TACCACAACACCTGG | 10533 |
| rs557055293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275927 | TGAGTGTGTGGTACA[C/G]AAAGGAAATCCTCTT | 10533 |
| rs557062885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11496309 | TCCCTGAATGGGTTC[A/G]CTGACCTGTAAGGAG | 10533 |
| rs557068157 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11405667 | ATCTCTCACTCTGTC[A/G]TCCAGGCTGGAGTGC | 10533 |
| rs557073491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503599 | CCATCTCTACTAAAA[C/T]ACAAAAATTAGCTGG | 10533 |
| rs557073697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11285521 | TAAAGTGCACTGATA[A/G]CAAATGTTTAGCTTG | 10533 |
| rs557086664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511659 | GGGGTGGTGCTCGTC[A/G]GGGAGGCTCCGGCCG | 10533 |
| rs557110874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443193 | GCGTGCTCCCACCTC[C/T]AGCCTGCTCAGCTGA | 10533 |
| rs557113769 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499343 | TTTCCAAAGATATGA[A/C/G]ATCATCAGAAGGAAT | 10533 |
| rs557115367 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11319603 | CCTCCCTCTGGACCC[C/T]GGGCCATATTATCCA | 10533 |
| rs557133607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348240 | TGGCTCATACCTGCA[A/T]TCCCAGTGTGTCTGG | 10533 |
| rs557146123 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11422840 | GCTCACTGCAACGTC[C/T]GCCTCCTGGGTTTAA | 10533 |
| rs557146504 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG7 | GRCh38.p7 | 3:11318894 | CTGGCTGATTGCTTG[C/T]GCCATTTCATTTCTC | 10533 |
| rs557152562 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271515 | CGTGAGCCACCGCGC[C/T]GGGCCTGCAGTAATC | 10533 |
| rs557153867 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11288879 | TATTGGTTAACCACA[C/T]ACGCTGCTATTTCAG | 10533 |
| rs557158233 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11395934 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10533 |
| rs557158380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402638 | GGCCAGCCTGGGCAA[C/G]ATAGTGAAACCCCAG | 10533 |
| rs557158640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11409257 | GCATTCATTAGAAAC[A/G]TATTTCAAATTGTGA | 10533 |
| rs557161964 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315726 | TGATACCTTACTCTT[C/T]TTTTTTGTTTGTTTG | 10533 |
| rs557165959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553081 | TGGGCAGGAGGTCCC[A/G]GAGGACACGGCCCAC | 10533 |
| rs557182107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11291180 | TTGTGGATGACTGAC[A/G]TATGTAGGGACTTGA | 10533 |
| rs557185100 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11414580 | AGGCCTTCTATTATG[A/T]TGTTGAAAAGGAGTG | 10533 |
| rs557191175 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11277894 | GGCCCTTTATAGACC[A/C]CCCCCCCCCCACCAG | 10533 |
| rs557194149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511004 | TGTTCAGATGTGTTC[A/G]GAGTTTCTTCCTTCT | 10533 |
| rs557194200 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292346 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAA | 10533 |
| rs557196728 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535687 | CCTCTCTCTTTTCAA[C/G]CAGGCTCCTTGGTAA | 10533 |
| rs557219953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377214 | AGAAGGGTTTCCTGT[C/G]TTGAATTATCTAAAA | 10533 |
| rs557243985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486210 | GTTTGTGTCCTCTTT[C/T]ATTTCATGAGCAGTG | 10533 |
| rs557246226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11408627 | ACAATCCTGGTGGAA[A/G]GTAAGGAGGAGCAAG | 10533 |
| rs557253801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11388611 | TTCTTTGTACTTTTA[A/G]TAGAGACAGGGTTTC | 10533 |
| rs557267290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11528703 | TGGTGGTGCGCACCT[A/G]TAGTCCCAGCTACTC | 10533 |
| rs557280475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511412 | CTAGATACAGAGTGT[C/T]GACTGGTGCATTCAC | 10533 |
| rs557282787 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436586 | CAGAGAAATGAAAAT[A/G]TGCACACAAAAAATG | 10533 |
| rs557287384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507546 | AAATACCTATAATTT[A/C]TGTTATTGACAGAGT | 10533 |
| rs557298982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468518 | CTGGGCCACTGAGGA[C/T]AAGCTGACAGGTCAG | 10533 |
| rs557300204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521905 | GAATGACTCTAGACT[A/G]CCGCCGCTGCCGACA | 10533 |
| rs557310519 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11306945 | CTCTTGTATCTAGGA[A/G]TGCTCCCACCCCAGC | 10533 |
| rs557330094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288419 | GATGAGTAAGACATG[A/G]TGCTTGTTTCAAGGA | 10533 |
| rs557338845 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11304410 | GAGGATGTTACAAAC[-/AG]AAACTCTGCGATTGC | 10533 |
| rs557344106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11321399 | CCACCAACAGCTGGG[A/G]CTGCCATGGTCTCAG | 10533 |
| rs557358125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11284733 | ATTTTTTAAAATTAT[C/T]TGTGGAGATGATATC | 10533 |
| rs557364277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370622 | TTTCTCAGAATGGCT[C/G]TTTGTTGCTGGGCAT | 10533 |
| rs557365807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422572 | TAAAACTTTCTCTGT[A/G]GCTCTTTTACTTTAT | 10533 |
| rs557366842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287742 | TTTGCAGCATTACAA[A/G]GTGCCTATTGCAGGC | 10533 |
| rs557371768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11429809 | AAAATCTAGCCCGGT[A/G]TGGCAATGTGCGCCT | 10533 |
| rs557373449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500876 | CCTTGTGATCTGCCC[A/G]TCTTGGCCTCCCAAA | 10533 |
| rs557388869 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11341079 | CCCGTCCCCCACCCC[A/G]CCCCAGACAGAGTCT | 10533 |
| rs557392186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334880 | AAGAATCGCTTGAAC[C/G]TGGGAGGTGGAGGTG | 10533 |
| rs557398413 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408783 | ATGATTCAGTAGTCT[C/T]CCACTGGGTCCTTCC | 10533 |
| rs557410733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392286 | TTTGGAGGGCAGGGA[C/T]ATGCAGCTGCTAAGA | 10533 |
| rs557412012 | in-del | -/AAAA | 0.022643 | 0.103965 | intron-variant | ATG7 | GRCh38.p7 | 3:11392475 | AAAAAACAAACAAAA[-/AAAA]AAAACAAAACAAAAC | 10533 |
| rs557412194 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438683 | GATTGGTAGTTATGA[A/G]TCCCTTTGAATTATT | 10533 |
| rs557413259 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11536503 | GTTTGTGCCTTCCAG[G/T]CTGGGGAAGAAGCCA | 10533 |
| rs557413292 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414968 | ACGATGGGGATACCT[G/T]CTGAGAAATGTGTTT | 10533 |
| rs557423074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11513103 | TAGATACAGAGTGCC[A/G]ATTGGTGTATTTACA | 10533 |
| rs557443068 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11478748 | ATGATCTAATCAGTC[C/T]TCCTTATGGAGAAGT | 10533 |
| rs557449203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11385644 | TACGGCATCCCAATA[C/T]CAATTAATTTTGTAA | 10533 |
| rs557450296 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11516448 | AACACTGACAACACC[A/G]AATGGTAGTGAGAAT | 10533 |
| rs557476447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425538 | TTCTGAGGCATTCTG[G/T]TTCAGCGTTCTACGT | 10533 |
| rs557490718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11477525 | CAAACAAAAAGTTGC[C/T]GCAAAAGATAAGGGC | 10533 |
| rs557496667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353708 | GGCATCTCTCTTTTT[C/G]CCTCCCTTGCCATGT | 10533 |
| rs557497423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364244 | ATTTTCCACTTCAAA[C/T]TTTCAGTACAGAAAT | 10533 |
| rs557502539 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11274386 | GGAGGACTTAGGGTA[C/T]GCATAAGTCAGGCTG | 10533 |
| rs557513722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537001 | TGTCGCTTCCTGCCC[A/G]AGTTCTGCAGTTTAG | 10533 |
| rs557519243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11344096 | CTCCCGTTAAACTTT[C/T]CAGTTGACTATTACT | 10533 |
| rs557542286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450294 | GTGTCTTTCTTACAT[A/G]TTAGTTGGGCCTGTG | 10533 |
| rs557549802 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372344 | CTATGGAACACTAAT[-/G]TTGGTGATTATTTTG | 10533 |
| rs557550344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456699 | CCACTGTGTCTAACA[A/G]AAGCCACAATTACTG | 10533 |
| rs557552953 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11491473 | TTCTTCTCTCAACTC[A/G]TCAAAGTCATTCTCC | 10533 |
| rs557557558 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11303995 | ACTCGGGAGGCTGAG[G/T]CAGGAGAAAGGCGTG | 10533 |
| rs557559049 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11418986 | CCCCGATCCAGTCAC[C/T]GCCCACCAGGTCCCT | 10533 |
| rs557570915 | in-del | -/TAGCTGTGCTG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11524204 | CAGGCTCCCCTTCAC[-/TAGCTGTGCTG]TGGCTTAGTTAAGCT | 10533 |
| rs557576702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493011 | CAGATGCCCTCCACC[A/G]GCAAGGGCAAAGGGC | 10533 |
| rs557578800 | snp | G/T | 9.45349e-05 | 0.00687448 | intron-variant | ATG7 | GRCh38.p7 | 3:11315304 | CCCAGAACTAGAAAT[G/T]TAATTTTCTAGAGAA | 10533 |
| rs557579895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412916 | TATAAGTCTTTCACC[G/T]GAAGTTAATTCCTAA | 10533 |
| rs557584297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519754 | TTTTAGTAGAGACGG[A/G]GTTTCACAGTGTTAT | 10533 |
| rs557584668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11416017 | GATTAGGAATTTTTC[A/G]GCTCCATTATAATCT | 10533 |
| rs557588901 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412445 | GATCTTGGCACTCTT[C/G]TCAAAAATTGAGACT | 10533 |
| rs557591666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281323 | CTAATCAGTATATTA[C/T]AACATTTCTCTAACT | 10533 |
| rs557596310 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11296077 | GCCACCGCGCCTGGC[C/G]TACTGGTTCTATTTC | 10533 |
| rs557603837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450798 | GCTTTCTTAGTTAAG[A/G]TCGTATTTTCTGATA | 10533 |
| rs557610446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11501571 | TGTGATAATGTTATT[A/G]TGGTTGTATAGGAAA | 10533 |
| rs557612889 | in-del | -/CAGAGCTGG | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11553358 | ACACAGCGTGTGGCA[-/CAGAGCTGG]CTACATGAATGTGTG | 10533 |
| rs557644122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322366 | GCTTTGTGACCATTT[A/T]ATGACCATTTTGGAA | 10533 |
| rs557646378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541715 | AGTTTTCCTCCTCCT[C/T]TTCTCCCTCTCTCTG | 10533 |
| rs557646390 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11440751 | TGCAATGGTGCAATC[C/T]TGGCTCACTGCAACC | 10533 |
| rs557655718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539538 | TAAATGAGTGGGAGA[C/T]TGCGTTGGTGCTTTA | 10533 |
| rs557660894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329156 | CCCATGTTTGTTTCA[A/G]AGTCCTAGTAATTAA | 10533 |
| rs557663474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515912 | AGACACTGCTGGCCA[C/T]GGGAAGTCTCAGCCT | 10533 |
| rs557678421 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11388514 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAT | 10533 |
| rs557686936 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498724 | TCTTTCCCCTTCTAA[G/T]TGCTCTTTCTCCTTT | 10533 |
| rs557691011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379662 | AACATTTTGGAAGAC[A/C]TTTGTTAAAAAATAC | 10533 |
| rs557710841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318205 | GGATTCAGGCACACT[A/G]TCCTTCACTTGGTTA | 10533 |
| rs557713175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495636 | GATCCACCTATGGCC[A/G]TATTTGAGGTTTCAC | 10533 |
| rs557733249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424970 | TTAATGGATGCAAAA[C/T]ATCCCTTTTTTTTGT | 10533 |
| rs557734310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456057 | TTTAATATTCAGAGT[C/T]GTGTAACCGTCATTG | 10533 |
| rs557734926 | snp | A/G | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11433424 | GTTATTTCTCATCCT[A/G]TGAGTAGAATAAGTA | 10533 |
| rs557755646 | in-del | -/TTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422765 | TTTTTTTTTTTTTTT[-/TTTT]TGGAGACAGAGTCTC | 10533 |
| rs557768970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325528 | AATACAAAATTAGCC[A/G]GGTGTGGTGGCGCAT | 10533 |
| rs557775412 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ATG7 | GRCh38.p7 | 3:11337484 | GCTCTCTCTCTCTCT[A/C]TCTCTATATATATAT | 10533 |
| rs557802694 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526169 | GCTGAGGTGGTCAGA[A/T]CGCTTGAGCTCAGGA | 10533 |
| rs557812273 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337916 | TACTAGGCTGTGATT[A/C]TGTAGTTCTTGTCAA | 10533 |
| rs557814274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11330948 | CCCTTCTTTGATTTT[C/T]TCATTGCATAAAAAT | 10533 |
| rs557823495 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555226 | GCCCAGAGCCACTGC[A/G]GGAGGTGGCACCCTC | 10533 |
| rs557825223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295567 | GCAATCTACAATGAA[A/G]TTGCATTTTAGAAAG | 10533 |
| rs557837848 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11383677 | CTGGTCTCTAACTGC[A/C/T]GACCTCGTGATCCGC | 10533 |
| rs557841927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11470952 | TCTCCAGTCATCTGC[A/G]TGGGATTTGTTTTCA | 10533 |
| rs557844136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353065 | ACTTGTTAAGTTATT[A/G]CAAGATTCTAATCTC | 10533 |
| rs557858809 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11276173 | ACCTCCTACCTTGAC[-/T]TTTGCTCCACTAAGT | 10533 |
| rs557861442 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11537458 | GAGCCAAACATATCA[C/T]AGCACATGGGGTACT | 10533 |
| rs557891396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345544 | TTAAAAATTAATTGA[A/C]ATAAAATACATATGG | 10533 |
| rs557907043 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11393843 | ATGCCACCACACCAG[C/G]CTAATTGTTGTATAT | 10533 |
| rs557908971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427543 | AAATTATCGGCCGGG[C/T]GAGGTGGCTCATGCC | 10533 |
| rs557917869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494964 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10533 |
| rs557919787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533038 | AAGCCCCAGCCTGAG[C/T]GGGAATGACTGGAGG | 10533 |
| rs557922282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431816 | TTATGAAGGAGGAAT[C/G]CAAAGCTGATCCAAC | 10533 |
| rs557927590 | snp | A/G | 0.000142346 | 0.00843521 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11333010 | AAGTTGTTTGCTTCC[A/G]TGACCGTACCATGCA | 10533 |
| rs557930972 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11490962 | GTCTTGGAGTTGCTC[C/T]TCTTGAGGAGTATCT | 10533 |
| rs557947279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367789 | TTAAGTCTCTGGCCC[A/G]ATGTACGTGGATTAG | 10533 |
| rs557966268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333362 | CTCCCCCCGTTTTCA[A/G]TTTTACTTTTCTTTA | 10533 |
| rs557981790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326252 | TAGTTTCTCCCTTCT[C/G]CCCCTTTTTACACTT | 10533 |
| rs557983934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11359644 | GAGGCTGCAGTGAAC[C/T]GAGATCACGCCATTG | 10533 |
| rs557996984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11434491 | AATCCCTCAAGACAC[A/T]GCCTTGGCCCTCTCT | 10533 |
| rs558005056 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11438094 | CCCTTGACACCCTCA[C/T]GCTCCTCTCTAAATG | 10533 |
| rs558005149 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11550784 | GCCTTTTTGACTGTT[G/T]TCCCGTGCATATTGC | 10533 |
| rs558010530 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441184 | TCCTCTTTGAAAGAG[G/T]CCATACTTAATTTTA | 10533 |
| rs558019345 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11296069 | AGGCATGAGCCACCG[C/T]GCCTGGCCTACTGGT | 10533 |
| rs558019828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551453 | AAGGGGTGTGGCTCT[A/G]TCTACTCCAGTTTAC | 10533 |
| rs558022866 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456403 | GTAGGCATCTGGATT[A/G]TTTCCACTTTTTTGC | 10533 |
| rs558030699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11382294 | TATATATAGAGAGAG[A/T]GAGTGCGAGCACGCA | 10533 |
| rs558044431 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11545227 | AGTTTGGACTTCACT[C/G]TCCCTCTGTGCAAGG | 10533 |
| rs558045444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544022 | GCCTTCCCTGCTTTG[C/T]GCAGTCTGCCTGCTC | 10533 |
| rs558049720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331798 | TAAAATAATTAAAAC[A/G]GAGGATATCTTAAAA | 10533 |
| rs558069783 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495504 | CTGCGCTGTTGGTCA[A/G]TAGAGAGAGGGTGCC | 10533 |
| rs558079194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11420676 | ATAAAAGTTACATTT[C/T]TACTATACTGTAGTC | 10533 |
| rs558082063 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11538759 | CAGGCCTGTGGTTGC[A/G]GCTACCCAGGAGGCT | 10533 |
| rs558087075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444104 | ATTCTTTCGTGTCTT[C/G]TTTTGCCCAATATTG | 10533 |
| rs558095976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330734 | TTCAAAGAGCTGTGA[A/T]AGCAGCAAGGACAGG | 10533 |
| rs558111760 | in-del | -/ATTTTCAATGTGAAAAG | 0.00716266 | 0.059414 | intron-variant | ATG7 | GRCh38.p7 | 3:11539000 | TCTGAGCTTCTTGCT[-/ATTTTCAATGTGAAAAG]CTTTAATCTGGCTGT | 10533 |
| rs558133440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544489 | GTCCCTGTGGCCTCT[A/G]GCCCAGAGCCAACCC | 10533 |
| rs558137092 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556416 | CCCTCCCAGAGTGAC[A/G]CCCTTGTTCACTGAC | 10533 |
| rs558148972 | in-del | -/CT | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450998 | AGTATATTGCCTTGC[-/CT]GTACCAAATACAGTC | 10533 |
| rs558156494 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11523497 | TAGGCAGAGGTGATA[G/T]GCACTGAAGTGTTTG | 10533 |
| rs558179566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473670 | GAGTCACTTCTGAGT[A/G]CTGTGTGATATCATC | 10533 |
| rs558184034 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11457607 | GGGGAAACATTTCCG[A/G]AACATACATTAAGAA | 10533 |
| rs558189357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11408543 | TGATAAAGACATACC[C/T]GAGACTGGGCAATTT | 10533 |
| rs558196393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399246 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 10533 |
| rs558198758 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11364790 | GGGGGAAAGCATGTG[A/G]GGTCTCTTTGCCATT | 10533 |
| rs558207350 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11413744 | GCTACTGCTGGCCTC[-/AT]AGAATGACTTAGGAA | 10533 |
| rs558212716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318731 | CTCATTTAATATTTC[C/T]CAAGATACATCCTGT | 10533 |
| rs558215254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479865 | TACTAGAATATGAAA[C/T]AGTGATTTGAAGGGG | 10533 |
| rs558232300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530006 | TTGAAAGTGCATGTA[C/T]GTGTTTTGGACAGAG | 10533 |
| rs558242940 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11323432 | GTAGTATTGTACACA[A/T]GTGTTAGGTTGAAAA | 10533 |
| rs558244290 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11307804 | CCAGTCTTTATCACG[A/T]CATGAATCTTGTTGG | 10533 |
| rs558280701 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11354465 | TCCATCCTGGCCAAC[A/C]TGGTGAAACCCCGTC | 10533 |
| rs558282399 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464981 | ACAGATGCCACATCT[A/G]TCATCATCGTCATCA | 10533 |
| rs558297986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516859 | AGGCTGAGGCAGGTG[A/G]ATCACTTGAGGTCAG | 10533 |
| rs558303001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484933 | CACATTTTCTTAATC[C/T]AGTCTATCGTTGTTG | 10533 |
| rs558320313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335710 | ACATTTTTTTTGCTT[C/T]TTTTGAGACAGAGTC | 10533 |
| rs558328610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402021 | TGTACAACTTGGTGG[A/G]TTTTTTTTCACATGT | 10533 |
| rs558329357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339717 | TACAGCAGTGTTTCC[C/T]TGAATGTGTCCCTTG | 10533 |
| rs558335166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381692 | AGAGTCCTGCTTTAC[A/G]TAAACATGTTGGACG | 10533 |
| rs558344448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11548545 | ATAGGGAGGCATTTA[A/G]ATTAATTTCTCCTTT | 10533 |
| rs558349339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322273 | CTTTTTCTGTTTTAT[C/G]TTTTTGAAAAATTCT | 10533 |
| rs558358689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336079 | CAGTCTCGCTCTGTT[G/T]CCCAGACTGGAGTGC | 10533 |
| rs558364584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290105 | TAGGGCTCCCCTCCA[A/T]TTAGTGTTCCAGCTC | 10533 |
| rs558367852 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11403182 | CCACCCATTGTAAGA[A/C]TAGAGTCTGATAATT | 10533 |
| rs558373284 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11396047 | CACTAGCATGTTTAC[A/G]CAAAAGGACTTTTAT | 10533 |
| rs558381905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341752 | TGTGCCTGGCCTGAG[C/T]GCAGGAGATATGGGA | 10533 |
| rs558382244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11283180 | TGTAGTGGGAGACTG[A/G]CCATTTCCTTTTAAT | 10533 |
| rs558392999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11346404 | TAAGATTCTAGAAAC[A/G]TACTGCCAAATTGCT | 10533 |
| rs558394469 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520283 | TGGCAAGCCCTGGTT[G/T]ATTAAAACTTTCCCA | 10533 |
| rs558397057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426605 | CAAACTGGAAGATAA[C/T]GTTATTGTTATTCTA | 10533 |
| rs558401601 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479310 | TTAAATTAAATGTTG[C/T]AAGAGATTACCATAT | 10533 |
| rs558407556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394526 | AAAAGGAAGTTGAGA[G/T]CGTGAGCCACACCTT | 10533 |
| rs558417236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553695 | GCAGTCCCCTCCCAA[C/G]AGCTCAGATAGTTTG | 10533 |
| rs558430663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11293856 | ACTCCGTATCGAGAG[A/G]AAAAAAAAAACATTA | 10533 |
| rs558449243 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11494198 | TCCCTGACTAAAATC[-/AG]GGGTTTATATGCCAG | 10533 |
| rs558455122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11438134 | AATTACCCTATTAGG[C/T]AACATGCCCCTGAGG | 10533 |
| rs558466322 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | ATG7 | GRCh38.p7 | 3:11545963 | GGCAACATAGGGAGA[-/C]CCCCATCTCCACAAA | 10533 |
| rs558467570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387449 | AATTTTTTCTTACAG[A/G]ATCCCTTTTGCCACT | 10533 |
| rs558479644 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558113 | TTCAAGTATACACAC[A/G]CACACACATGGACCG | 10533 |
| rs558480879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457582 | TTTGCATTCTTTGCC[A/T]CCGGATCAGGGGGAA | 10533 |
| rs558493855 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392287 | TTGGAGGGCAGGGAC[A/G]TGCAGCTGCTAAGAA | 10533 |
| rs558512525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11356410 | CTGGGGAAAAGCCTG[G/T]CCATTAAACTCTCTA | 10533 |
| rs558527722 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317035 | TTATTAGAGATGGGG[C/T]TTCACCGTGTTAGCC | 10533 |
| rs558544680 | in-del | -/CCAAACAC | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11558130 | CACACATGGACCGAA[-/CCAAACAC]CCAAACACGCCGTGG | 10533 |
| rs558547053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349001 | TTTTACAGAGTGCTG[A/C]TTGGTGTGTTTACAA | 10533 |
| rs558585345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468693 | CTGTGACCTGTTCCT[C/T]TAAATGCCTGTGGGA | 10533 |
| rs558597506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11307981 | GGAGTCTCCAAAGAA[C/T]TGGGTCAGGCCTTAA | 10533 |
| rs558624139 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11319005 | CCATATCCCCAGCCT[A/G]TGAGCAACTTTAGCA | 10533 |
| rs558635674 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450977 | CAAGATCTGTAGAGA[A/C/G]ACCTTAGTATATTGC | 10533 |
| rs558636802 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11346788 | TTAGATGATGAAAAT[A/C]ATTTACAAAACTGGG | 10533 |
| rs558639555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402576 | ACCTAGAACCTCCTT[A/T]TACATTCATTAACAT | 10533 |
| rs558645973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372083 | TGTCCTGTCTCCTAA[A/G]GCCCTGTGAGCCAAG | 10533 |
| rs558648474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486409 | TGAGACTTTGCTGAA[C/G]TTGCTTATCAGCATA | 10533 |
| rs558655783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11396746 | GAGATGGCGCCACCG[C/T]ACTCCAGCCTGGGCT | 10533 |
| rs558666304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ATG7 | GRCh38.p7 | 3:11272523 | CTCGCCAGGGAGGGC[A/G]AGGGTCACAGCAAGT | 10533 |
| rs558685516 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11296383 | TTCTCTCTTTTCATT[G/T]CTTGAGTCCACCAAG | 10533 |
| rs558690036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11469418 | CGTGCCACTGCACTC[C/T]GGCCTGGGCAACAAG | 10533 |
| rs558702356 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11377127 | CTGACAGCTGAGCCT[C/T]TGCATTAGCTAGAAG | 10533 |
| rs558703442 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11289775 | ATGTTGCCCAGGCTC[A/G]TCTCAAACTCCTGGG | 10533 |
| rs558707343 | snp | A/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11434435 | CAACCCATGCTGGCC[A/G]TCCTGGGACTGTGCC | 10533 |
| rs558710193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11487023 | TACTTGAGATGAGGG[A/T]TTGGTGATGACTCTT | 10533 |
| rs558719168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323901 | TGTTTGAGTTCTAAA[C/G]ACAGCCATTTGTTAG | 10533 |
| rs558728366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452592 | ACTTCAGCAAACAGC[A/G]TGGTAGGGAAAAGAC | 10533 |
| rs558728712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423342 | TCACCACAACAGATA[C/T]AATAATAATGAAAAA | 10533 |
| rs558732472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11364027 | AGAGCTGACTTTATG[C/T]TTCCTTGACACTGAG | 10533 |
| rs558743608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542348 | CCATTTTCCAGACTA[A/G]TAAGAGGGGGAGACC | 10533 |
| rs558753850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11499577 | GTGGTGAAACCCTGT[C/T]TCTACTAAAAATACA | 10533 |
| rs558757834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423928 | TGTCCTGACCAGAGG[C/T]GTCAGATTGTTCCAC | 10533 |
| rs558762598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483991 | TAGCACTCTTTGATA[C/T]AGGGTAGAATTTGGT | 10533 |
| rs558766113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11469922 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGT | 10533 |
| rs558768586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391895 | TCACTTTTCTACCAT[A/G]TTAATCATCTCTCAG | 10533 |
| rs558769126 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11405280 | TAAACTCCACCCCCA[C/G]CCCCTTGCCCCCACT | 10533 |
| rs558783618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11286428 | ATGATTCCTTACTCC[A/G]TATTCTGTGGTAATT | 10533 |
| rs558791985 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11525144 | TGGGCTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 10533 |
| rs558794318 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534036 | GTGAGCCGTGCCACT[C/G]TCAGAGTTGGAAAAG | 10533 |
| rs558803611 | in-del | -/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326297 | TGCTGTTTTTTTTTT[-/G]TTGTTGTTGTTTTGT | 10533 |
| rs558805297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301441 | TTTAAAATAAAGTGT[C/G]CCTAGAATTTTTTTT | 10533 |
| rs558824357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285898 | TTTATAGTGGAGCAT[A/C]ATCCCAGGATCACAC | 10533 |
| rs558833774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537111 | CGTGCTCTGCTGTCA[A/G]CCCCCCGGAGCCCCT | 10533 |
| rs558839819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293267 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10533 |
| rs558843098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445844 | AATTTTTGCCAATCT[G/T]TATAACAGTATCATA | 10533 |
| rs558869543 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11390324 | TAATGTCTGAGTAAG[A/C]AAACAAAAACATGTG | 10533 |
| rs558911076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351639 | TGTGTTACTCTGTTT[C/T]CCCTGTTGGACTATT | 10533 |
| rs558926803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11483339 | TCACCATATAGTCTT[C/T]CTAAGAAGAATCAGA | 10533 |
| rs558927104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11398492 | TAATTAAGGATGACA[C/T]AATGGAAATTAAGAA | 10533 |
| rs558928711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451482 | TCCCAAAGTGAAAGT[C/T]GGCATTACTAGCCCT | 10533 |
| rs558933094 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272121 | GATCATTCCTGTCAT[C/G]CTCTGAAATCAAAAG | 10533 |
| rs558970968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491032 | CTACCTTGCTAGATT[C/G]GGGAATTTCTCCTGA | 10533 |
| rs558978288 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11417389 | TTAAGAACTGTGTCT[C/T]ACTGGAGAATTGAGC | 10533 |
| rs558993374 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374127 | CAAATTCATATGGAA[A/G]TGCAAGGGACCCAGA | 10533 |
| rs559001283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378156 | GGAGCTGGGATTACA[C/T]GGGTGCACCACCACA | 10533 |
| rs559008094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404492 | CCATTAATACCTCTG[C/T]CTTGCCTTTTATCTC | 10533 |
| rs559015250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279272 | AACATTCTGCAGTGT[A/G]CAGGGATAGCTCTAA | 10533 |
| rs559021967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11367069 | TTAGCTACTTTCTAA[A/G]AAAGAAAGTGGAGAA | 10533 |
| rs559028807 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459582 | TGTAACTTCATGGTT[C/T]CTGGAAGCCAGAGCC | 10533 |
| rs559030853 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11451851 | TATCTCTCTCTCTAT[A/C]TATATATACGCCTTT | 10533 |
| rs559036474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11315908 | TTTTTTGTATTTTTA[A/G]TAGAGACAGAGACGA | 10533 |
| rs559040655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410383 | CAATTCAGAAATTTG[C/T]CTTGTTGACAAATGT | 10533 |
| rs559055805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278582 | GTGCGAAGACTGGTG[A/T]TAGAAAAACAATGAC | 10533 |
| rs559061307 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11303533 | AATTAGCCGGGCGTG[C/G]TGCCGGCGCCTGTAG | 10533 |
| rs559068803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405703 | TGTGATCATGGCTCA[C/G]TGCAGCCTCAACTTC | 10533 |
| rs559069240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416771 | TTTGCTGCTCTTGTT[A/G]CCTAAGGTGTAAGAT | 10533 |
| rs559087282 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11535275 | ACCCTGCCTGGTGTC[A/G]TCTGAGGTGTCCTTT | 10533 |
| rs559125415 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555930 | TTCAAATGAGGCTTC[A/G]CTTCTCCCAAAGTAG | 10533 |
| rs559129177 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11551935 | TGGATTTTTAGTAGA[A/G]ACGGGGTTTCACCAT | 10533 |
| rs559137740 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426410 | GCTCGTATGTCACAC[-/T]TTTTTTGACAAAATC | 10533 |
| rs559144907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310383 | CAAGTTTTCCTTCCC[C/T]GACCTCCCACCGTTC | 10533 |
| rs559150181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509292 | AGCCGAGCTGTTCCC[A/G]GCCCAGATAACACTT | 10533 |
| rs559161152 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11457325 | AGCAGCTGCTGTGAA[A/C]TGAGTGGTGTGGCAA | 10533 |
| rs559170773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289022 | CACAATCCCATCTTG[C/T]GTAACTCAGGATGTT | 10533 |
| rs559171873 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381443 | TGAAATAAAGATAAT[G/T]GGGTTCTCTAAGTGA | 10533 |
| rs559177482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458630 | ATAGCTAGTTACTTC[C/T]CCATGCTGGAACTCA | 10533 |
| rs559187459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393554 | GTATAATGTTGCCAG[A/C]CATTCATGAGTGACT | 10533 |
| rs559206955 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11398047 | CGAGATCACACCACT[C/G]CACTCCAGCCTGGGG | 10533 |
| rs559216693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439821 | GAAGAGTACCAAGAG[A/G]GGTATAGCAACTAAT | 10533 |
| rs559233557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445176 | ATAAACAGAAATACC[A/C]TTTGACCCAGCAATC | 10533 |
| rs559240360 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11433884 | CAACCATAACATAGG[C/G]TATAAAATCATAAAC | 10533 |
| rs559252226 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11554537 | TCAGGGACGGTCCCC[C/T]GAGGTGGACATGCAG | 10533 |
| rs559273342 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315748 | GTTTGTTTGTTTGAG[A/T]TGGAGTCTCGCACTG | 10533 |
| rs559304663 | snp | A/G | 1.66585e-05 | 0.00288599 | intron-variant | ATG7 | GRCh38.p7 | 3:11426956 | AGCTTTCTGTAGTGA[A/G]GACTGACATGCTTAA | 10533 |
| rs559317205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473077 | CTTTCTGATATTCAG[C/T]CCTGACTGCCACTTG | 10533 |
| rs559334337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413815 | GTGGTACTAGTTCTT[C/T]AAATGTTTGATAGAA | 10533 |
| rs559336293 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11424095 | AGAGCTCCCCTGCCT[A/C/G]CCGTCGCCTGGTCCT | 10533 |
| rs559344982 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11342707 | TTCCATAGTATGTAT[A/G]TGTAGTATTTTGTTG | 10533 |
| rs559361226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446821 | AATCACTGGTCTCCT[A/G]GACTGGGCCATGAGT | 10533 |
| rs559365444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274664 | TTTGGGATCCAAGAT[A/G]GCTGCGTACCAATAT | 10533 |
| rs559367555 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11325687 | AAAAAAAAAAAAAAA[A/T]TTTATCCTATAGATG | 10533 |
| rs559369234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534181 | ATGTTCAATCTGAAT[A/G]AGAAAGGAACTGGAG | 10533 |
| rs559390351 | in-del | -/TTTT | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11284850 | CCACTGTGCCTGGCC[-/TTTT]TTTTTTTTTTTGAGA | 10533 |
| rs559394520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11344422 | ATTTCTGTTTCTGCA[C/T]GTTTATATCAGAAAT | 10533 |
| rs559398797 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415760 | GGAATGCAGTTAACT[-/T]TTTTTTTTTTTTTTA | 10533 |
| rs559402743 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297458 | AGTGAAGGGACCTTA[C/T]CAATTTGCTTTTTGG | 10533 |
| rs559428119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11311369 | AGCGATTTGGGAGGC[C/T]GAGGTAGGCGGATTG | 10533 |
| rs559432818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289718 | GCGCCCTGCAATGCC[C/T]GGCAAATTTTAAAAC | 10533 |
| rs559433597 | snp | A/G | 0.000819734 | 0.0202286 | intron-variant | ATG7 | GRCh38.p7 | 3:11426971 | AGACTGACATGCTTA[A/G]AACTATTTGATATTC | 10533 |
| rs559437054 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11284655 | TGCCTGGGCTCAGGC[A/G]ATCCTCCTGTCTCAG | 10533 |
| rs559442039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538906 | AAAAAGCCCTTAGTA[A/G]TTCTTGAGAATGAGT | 10533 |
| rs559450722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298023 | TCTCTACCAAAAATA[C/T]AAAAAATTAGCTGGG | 10533 |
| rs559460540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412366 | AGAAGGGTCAATTTC[C/T]ATGTTTATCCAAAAA | 10533 |
| rs559476489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11326681 | AGTTGTGTGGCAGAC[A/G]CTATCTGTCATGATT | 10533 |
| rs559491341 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11310861 | ATGGTCTTGATCTCC[C/T]GACCTCGTGATCCGC | 10533 |
| rs559491396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318423 | ATACGGGTGATACTT[C/T]GGTTGGTCTTCTATG | 10533 |
| rs559498335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529008 | ATGGGAACTGCAAAG[C/G]TGGGCCTGGAGGACA | 10533 |
| rs559504430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407572 | CAGAGGTTCTCCATG[A/G]GGACCCCACCCCTAC | 10533 |
| rs559507358 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315069 | ATGTTTCGTTACCGC[C/T]CTAAAACTCTGATTG | 10533 |
| rs559511304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11540144 | TCAAATTCACTGTGT[C/T]GTTTTTGCTGTTGCC | 10533 |
| rs559520239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11357533 | GAGTTTTTTGTATTT[C/G]AGGTTTTTTAAAATG | 10533 |
| rs559523247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275552 | TTTAGTAGAGATGGG[G/T]TTTCACTGTGCTAGC | 10533 |
| rs559528797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11514830 | AAGTTGCCAAGTGCA[C/T]CTGGTCTAGGTTTTT | 10533 |
| rs559544615 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11407697 | GCAGGCTCAAAACCA[C/T]GTGGAAGCTGTCAAG | 10533 |
| rs559546964 | in-del | -/CACC | | | intron-variant | ATG7 | GRCh38.p7 | 3:11475906 | ACACACACACACACA[-/CACC]CCCTCCCAGAGTCCG | 10533 |
| rs559553902 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11506160 | ACTGAGTCCAGGTAC[A/G]TTTGTGTATTAGTTA | 10533 |
| rs559557241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400087 | TCATTTACACTGTTC[C/T]TTATGCCAGACAGGA | 10533 |
| rs559557425 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439204 | CTCCCGAGTAGCAGG[A/G]ACTACAGGCGCCCAC | 10533 |
| rs559559652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313797 | TAGATATGGGGTTTT[C/G]CCATGTTGGCCAGGC | 10533 |
| rs559564394 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341852 | TGGTGTGTTTTTATT[A/C]ATGGACACCATGATT | 10533 |
| rs559565705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11520267 | GCTCCTCTACCATGA[C/G]TGGCAAGCCCTGGTT | 10533 |
| rs559571566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381203 | AGTTTCCTTTAAGAT[A/G]TATCTGCTCAAGCCA | 10533 |
| rs559578331 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406552 | GCTTCAAGCAGTCCT[C/T]TTGCCTCGGCCTCTG | 10533 |
| rs559590203 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557167 | GACCAAAAAGGAGCA[A/G]CTGTGACCTCCACAG | 10533 |
| rs559600005 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11481640 | ACCTTTCCTGGGTTG[G/T]GCCTTGGACTTAATG | 10533 |
| rs559602367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339188 | GTACTCCCAGCTACT[C/T]GGGAGGCTGAGACAG | 10533 |
| rs559624321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313126 | ACTATTTTGGGAATA[C/G]AAAAGTCCTTTATTT | 10533 |
| rs559626190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11320436 | GAGATTACAGGCATA[C/T]GCCACCACACCTGGC | 10533 |
| rs559654019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354217 | GACCCTTTCCAGGTG[A/C]CTTTAAAAAAGCTAT | 10533 |
| rs559654621 | in-del | -/CTGCC | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11358196 | GTATGTCTCTGTTTG[-/CTGCC]CTGCCCTGCCCTGCC | 10533 |
| rs559658972 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535402 | TGTGGAGGAACCCTG[A/C/G]CTTTTGTGATTCTCA | 10533 |
| rs559666530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381752 | AGCTGTGCTATTCCC[A/C]TAGCGGTCACTTTTC | 10533 |
| rs559666562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528339 | TAAAAAAACATAAGA[G/T]AGCTATCTTACCTTC | 10533 |
| rs559668003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11441000 | CATTTGCTTTTATTC[A/G]GCTATCTGGTGAAAA | 10533 |
| rs559672793 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11447891 | ATGGGGGATGGTCCT[C/T]CTCAACAAACTGATG | 10533 |
| rs559692271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11347399 | AGAAATGGTACAAAA[C/T]GTTCTAAAATATCAT | 10533 |
| rs559723095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345176 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCATGAGG | 10533 |
| rs559727475 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397121 | TTGGTTAAATGCTGG[C/T]GGTAGAAAGATTATC | 10533 |
| rs559730684 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11441569 | TAAAGCACCAGTTTG[A/G]AACCAATCTTTTAGA | 10533 |
| rs559734905 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538575 | GTGCCAGCCTCAGGG[C/G]CTCACACCTGTAATC | 10533 |
| rs559737330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11306743 | GAGTATAGGGAATAT[A/G]TAGGCTTTTAGGGGG | 10533 |
| rs559769662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407160 | ATACAGCCATTCCAA[A/T]TTGGAGAAATTGACC | 10533 |
| rs559791272 | in-del | -/AAAAAA | 0.233527 | 0.249457 | intron-variant | ATG7 | GRCh38.p7 | 3:11469989 | ACGAGACTCCATCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 10533 |
| rs559793538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11473895 | ATCAGCGAGCCCTCA[A/G]TTTCTGTGCATACGT | 10533 |
| rs559796902 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456175 | CTAACCCTGAGCGAT[A/G]ACTAATCTTTCGTCT | 10533 |
| rs559802481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11293574 | AATGACTGGCCGGGC[A/G]GGGTGGCTCACATCT | 10533 |
| rs559829916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11427865 | TGCTCGCTGTTCTTA[G/T]AAAAGGGAATGCTGT | 10533 |
| rs559832273 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430379 | TAGTGTTTTGATTTA[A/C]ATACTTGATTCTCAA | 10533 |
| rs559838777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11448489 | ACATGTGCCTTTAGT[C/T]TCCTCCATAGTCTAA | 10533 |
| rs559844842 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11400235 | CCTTAGGCTGTAAGA[A/G]ACTGAGTCCAATGTA | 10533 |
| rs559852618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378331 | CAAATTTTTAAAATG[C/T]CTTTATCAATATGCT | 10533 |
| rs559853022 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11536194 | TTGGAGGAGAACCGA[A/G]AGGTTTTCAGTAGAT | 10533 |
| rs559867257 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11449057 | CCTTCATTGAACTTA[C/G]AAATGGGAGGGAGAT | 10533 |
| rs559874858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551992 | GACCTCAAGTGATCC[A/G]CCCGCCTTGGCCTCC | 10533 |
| rs559875821 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349019 | GGTGTGTTTACAATC[C/T]TCTAGCTAGACACAG | 10533 |
| rs559883233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466395 | TTGTGTCCACGTCAT[A/G]TTGCAAAGGGCATGA | 10533 |
| rs559884604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11336273 | TCCTGAGCTCGGGCA[A/G]TCTGCCTGCCTCAGC | 10533 |
| rs559886517 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11444894 | ATTAAAAAGTGGGCA[A/G]AGGACATAAACACAC | 10533 |
| rs559892204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11395871 | CGTGAACCGAGGAGG[C/T]GGAGCTCGCAGTGAG | 10533 |
| rs559913504 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11383513 | AGAAACCTGCAATCT[C/T]GGCTCACTGCAACCT | 10533 |
| rs559923681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330076 | GACTGGGGTTATGGG[G/T]TTTTGGAAAAAATAC | 10533 |
| rs559927070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350625 | GCTCAACAGTGGTAC[A/G]GTGCAATGTCTTCCA | 10533 |
| rs559947165 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ATG7 | GRCh38.p7 | 3:11540908 | GTTTTAGCTTTTTTT[G/T]GGGGGGGGAGGGGGG | 10533 |
| rs559955574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316897 | AAAGCCTTTAACTGA[C/T]GGTCTGGTTATTCTT | 10533 |
| rs559965930 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419013 | CCCTCCCCTGACATG[A/G]GATTACAATTTTAGA | 10533 |
| rs559968224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537272 | CCCCAAGTCCCTTTC[C/T]AAAAGAACTGTTCCT | 10533 |
| rs559968958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485637 | TATGTCCTGAATGGT[A/G]ATGCCTAGGTTTTCT | 10533 |
| rs559969360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11497406 | ATTTAGCCAGGCATG[A/G]TGGTGGGTGCCTGTA | 10533 |
| rs559988922 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11394347 | AGCTCTCTTACTGAA[A/G]TCACCTTAAGAAACT | 10533 |
| rs559990555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547976 | CCTCCAGAGTAGCTG[A/G]GACTATAGGTGTGCA | 10533 |
| rs560001251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11454752 | GCCTGGCAGGTAGAA[A/G]GAAGCTCAGTGTGTG | 10533 |
| rs560012602 | in-del | -/TTTG | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11373015 | AGTATGGGTTATTGT[-/TTTG]TTTGTTTTGTCATGT | 10533 |
| rs560012876 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11384471 | ATTAAACTCCTCAAA[G/T]TGACTTGCTATTAGC | 10533 |
| rs560014785 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441875 | TTCACCATGTTGGCC[A/T]AGCTGGTCTTGAACT | 10533 |
| rs560016083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395114 | AAATCTAGAACTGAA[A/C]ATTCAAAAACAAAAT | 10533 |
| rs560026724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430754 | GAGCTCTAATGCAAT[A/T]AAAAATGTTTTAGTC | 10533 |
| rs560027351 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ATG7 | GRCh38.p7 | 3:11323253 | ATTGCAGGCTACCAG[C/T]GTGAAGTCCTGGAAT | 10533 |
| rs560029572 | in-del | -/AAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538704 | AAAAAAAAAAAAAAA[-/AAA]TTAGCCAAAAAAAAA | 10533 |
| rs560030959 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11369424 | CTTATTTCCCTCCCT[C/T]CAGCCATCCCCTCAA | 10533 |
| rs560036606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485956 | GTAGCCTTGTAGTAT[A/T]GTTTGAAGTCAGGTA | 10533 |
| rs560054542 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11421046 | AGGCGTGAGCCACCA[C/T]GCCTGGCCACAAAAT | 10533 |
| rs560058797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491728 | CTGTTGGAGTTTGCT[A/G]GAGGTCCAGTCCAGA | 10533 |
| rs560060943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11451749 | AAGAATTGGCAACCA[C/T]AGAAAATATTACGTG | 10533 |
| rs560069358 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11362506 | GAACTGAATTGAGTC[A/G]CTTAAAGGAACACAT | 10533 |
| rs560071356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410743 | GTCAGAATTTCCTTC[C/T]TCTTTAAGGTTGAAT | 10533 |
| rs560078835 | in-del | -/ATAC | 0.0126979 | 0.078662 | intron-variant | ATG7 | GRCh38.p7 | 3:11498154 | CATATATACACACAT[-/ATAC]ATACATACATACATA | 10533 |
| rs560079065 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554958 | CCCTCCTCCATACCC[C/T]GAGGTCTGGGATTCC | 10533 |
| rs560087493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329615 | GATACTTTCTGCTCT[C/G]CATATGCTCTTTGTC | 10533 |
| rs560104225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11499784 | AAAAAATCTAAAATA[G/T]CCCATGGTGCAGATT | 10533 |
| rs560108250 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444357 | GATAATTTAATGCCA[A/G]CAGTTTAGAATTTAA | 10533 |
| rs560115864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361975 | TCTCTTTTGGATGAC[A/T]GGCTTTTATGCCCTC | 10533 |
| rs560129329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337027 | TCCTCATGGTGTGTT[A/G]TGTTACAGCTCTGGC | 10533 |
| rs560129603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344365 | TATCTTTAATTTTGA[C/T]GTTGGTTTCTGGTAA | 10533 |
| rs560132502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278384 | ATTTGGGAACTGATA[C/T]ATGTCCATATTAAAA | 10533 |
| rs560140607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543029 | TGGTCTGCTGCCCCC[A/C]TCCCTGGAGGTGCCT | 10533 |
| rs560146252 | in-del | -/ATATATATATATA | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11497367 | AAATACTATATATAT[-/ATATATATATATA]TATATATATATATTT | 10533 |
| rs560147684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335823 | CAGACTCAGCCTCCC[A/G]AGTGGCTGGGATTAC | 10533 |
| rs560147939 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11375761 | GATGGGGTTTCACCA[C/T]GTTTGCCAGGCTGGT | 10533 |
| rs560148517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470519 | ACGTCATTATGTGGT[A/G]TGTCACTGCTTACTG | 10533 |
| rs560177871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383781 | CTCACTTGCTGAAGT[A/C]TAGAATAATACAGGA | 10533 |
| rs560192000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457703 | TTCAATTTGTGTGCC[C/T]CTCGCTTATGGGTGT | 10533 |
| rs560196853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445426 | CCTTACAAACTCATC[A/G]AGGAGCAGAAAACCT | 10533 |
| rs560214253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377741 | AAGTAAACTTAATAT[A/G]AAAGTAATTGGGGTA | 10533 |
| rs560220533 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468611 | CATGCTATGAACTGT[A/G]TCATGGAGAAAACAC | 10533 |
| rs560277606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403479 | TGTCTGATTCCTTCT[A/G]TTTAGATAATAAAGG | 10533 |
| rs560288558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11554474 | AACAAGCTGGCTTGG[A/G]GTGGGGGTGAGTGCT | 10533 |
| rs560288845 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535284 | GGTGTCATCTGAGGT[A/G]TCCTTTACCTGCCTG | 10533 |
| rs560309491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432091 | GGGAGAGGTCAATGT[A/G]TGAGGGTGCATAGTG | 10533 |
| rs560325649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478341 | TATTCATCTGAGTTT[C/T]AAATGATTGCCTAAT | 10533 |
| rs560331610 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11479167 | TGATGCCAATTTTCT[A/T]TTCACATATATGAAA | 10533 |
| rs560336253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309394 | CTAAATAAAGGAAAG[G/T]TGCTTCTGGATTAGA | 10533 |
| rs560343214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11465668 | TACTTGGAGAACTGA[A/G]GGGGAAGGATTGCTT | 10533 |
| rs560360570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310035 | GCTGGGTGTGGTGGC[A/G]CCTGCCTGTGGTTCC | 10533 |
| rs560364023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11365947 | CTTGTGGGCCGGGCG[C/T]GGTGACTCATGCCTG | 10533 |
| rs560367873 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11471251 | CTACCGCTGGCCCCA[C/G]CTTCCTCTCAAGCTG | 10533 |
| rs560374191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11488639 | GCCTTCTGGGGCCTC[C/T]GGCGCCGTGACCTCC | 10533 |
| rs560374540 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11493709 | TAGGTAAATACTTAG[A/G]TACAAAAAACAAAAG | 10533 |
| rs560380098 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11342836 | TATATATCCATAGGA[-/T]TTTTTTTTTTAGGAA | 10533 |
| rs560383099 | snp | A/T | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11525582 | TTTTTTTAAACGGAG[A/T]CTTGCTCTGTCGCCC | 10533 |
| rs560415373 | in-del | -/GCCCTAGGCAGCCATTGGTT | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11521178 | TTTCAGATCAGTAGA[-/GCCCTAGGCAGCCATTGGTT]GCCATAGGCAGCCAT | 10533 |
| rs560428123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11351173 | TATTTAAGACCTCCC[A/G]TGTTCCAGGGACAGG | 10533 |
| rs560451896 | snp | C/T | 0 | 0 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272249 | CCGCCCCCTGATGCC[C/T]CGCCCTCCTCACGAC | 10533 |
| rs560454837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431391 | GCAAGGGCGGGGGGA[A/G]AAAAACAACCACACA | 10533 |
| rs560459331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493348 | CTCTGCCAGCTGAGC[C/G]TGGAGTCTTTATAGA | 10533 |
| rs560466322 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271877 | CAACACCTGTCCAGT[A/G]CTTTGCACGCGCAGA | 10533 |
| rs560498190 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11308724 | TGAAAATGGCCTGGT[G/T]GCCCCCTCGGTGCTG | 10533 |
| rs560499991 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11272403 | GCGCGCCTCAGAGAG[A/C]GCTGTGGTTGCCGGA | 10533 |
| rs560514323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11392492 | AAACAAAACAAAACA[A/G]AAAAACAAAAGCTTA | 10533 |
| rs560519583 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557344 | ACAGATTGTCTGTCA[A/G]TAATCTGCTGTTCAG | 10533 |
| rs560533621 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452918 | CACCTATTGTGTGCC[A/G]GTTCCTATCTGCTGG | 10533 |
| rs560537665 | in-del | -/TA | 0.0287284 | 0.116357 | intron-variant | ATG7 | GRCh38.p7 | 3:11451764 | AGAAAATATTACGTG[-/TA]TATATATATGTTTAT | 10533 |
| rs560538974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398288 | TTCTTTTCAAGCACA[A/C]ACATAATATTTTACA | 10533 |
| rs560560945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280728 | TATTGGTAAAATATG[C/G]TAATAAGAATACTTT | 10533 |
| rs560576082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385179 | GGACTACAGGCGTGC[A/G]CCACCACACCCAGCT | 10533 |
| rs560593286 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11474083 | TTCAGACTTACCAAG[C/T]GTGTAGTAAGCCAAG | 10533 |
| rs560602406 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11368211 | GTTCCTTCTTCCCAT[C/G]AACAGTGTTCTTTTA | 10533 |
| rs560610609 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523368 | CTTGGTGACCCACCG[C/T]ATACGGGGTACATCT | 10533 |
| rs560621422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508380 | TGTTTTAAGAAAGTT[G/T]ACAAATTTGTGTTGG | 10533 |
| rs560633866 | in-del | -/C | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556148 | CAAACCTTTTTTTTT[-/C]TTCTTCCAGGAAAAA | 10533 |
| rs560640828 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334378 | GCCTCCCAAGAAGCT[A/G]GGATTACAGGAGCCC | 10533 |
| rs560650274 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466727 | GTTCAATATCATCTA[C/T]AGAAACTCAACTGTT | 10533 |
| rs560663833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418412 | AGCCACTGTCCCCAA[A/C]CAACATATTTCAATA | 10533 |
| rs560674270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11419112 | TGAGAAATACATGCA[C/T]GTGTATTTTTTAAGT | 10533 |
| rs560676243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11411724 | TGTTGATGTTGTCCA[C/T]CTATGAAATTCAGTC | 10533 |
| rs560681074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11435000 | CATGTGAAATTCTTT[C/T]TTTAAGCCTCCTTTC | 10533 |
| rs560682330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538283 | GGCCTTTCTGAGGCC[A/G]GCACAGACTCTATCA | 10533 |
| rs560688277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501108 | AAAAATAAAAAATTG[G/T]CCAGGTATGGTGATA | 10533 |
| rs560689213 | in-del | -/AGTAAATACA | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11374013 | AATCACTGTGCTATG[-/AGTAAATACA]AGTAAATACAAGTAG | 10533 |
| rs560695732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354061 | TTTGCTCTAAAATAT[A/G]TGTATCCCAGACTAA | 10533 |
| rs560732375 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11371702 | CCACTGCTTCTGTCC[A/G]TGAAAACATGGCTTC | 10533 |
| rs560740011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340087 | GGAGAAGTCAGGGAA[A/G]GGAAACTTCTGAATG | 10533 |
| rs560743578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288060 | CAGACTGTTTGAGGC[C/T]TGCAGTGCCTTAAAA | 10533 |
| rs560767415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11458348 | CGCTCACTGCAAGCT[C/T]CGCCTCCTGGGTTCA | 10533 |
| rs560780319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287500 | ACAGGGCCGTGGGGT[A/G]GAACTAGAAAAGTCG | 10533 |
| rs560786392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485583 | GGCTTTTGTTGACAT[C/T]GCTTTTGGTGTTTTA | 10533 |
| rs560789608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330498 | CACCTTGGCATGCCC[C/G]AATTCATTTGTTTTT | 10533 |
| rs560790101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11528180 | ATTTCACGGGGCAAG[A/G]TTTTCTGCACTGAAT | 10533 |
| rs560805033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11474759 | GCCCGGAATGCAAAG[A/G]AAGGAGCCAGACATG | 10533 |
| rs560816567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379237 | GAGAGTTTAGAGATG[C/T]TACCATTCATATTTT | 10533 |
| rs560818396 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496507 | AGTTGCTCTTCTCTG[A/T]GGGCTGCTGAGGCTG | 10533 |
| rs560821553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521678 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10533 |
| rs560838956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549817 | AGACCTTCCTCCAAA[A/G]TGGTTTTGCCAGTTT | 10533 |
| rs560858500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515041 | AGACAGGGTTTCACC[A/G]TGTTGGTCAGGCTAG | 10533 |
| rs560865585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543790 | GCCTGTTATCCCGGC[C/T]ACTCAGGAGGCTGAG | 10533 |
| rs560867340 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11451739 | CATCTAGCATAAGAA[C/T]TGGCAACCATAGAAA | 10533 |
| rs560867741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467445 | GCAATGGTGCGATCT[C/T]GGCTTACTGCAACCT | 10533 |
| rs560874770 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523508 | GATATGCACTGAAGT[A/G]TTTGATTTAGAGTGA | 10533 |
| rs560894322 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11369164 | ATTTTGAAAAAATCT[A/C]TTTACTGTGTTCAGA | 10533 |
| rs560897947 | in-del | -/AATT | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11430491 | ACAATCAAGATGCTA[-/AATT]AATTCTCATTTTGGG | 10533 |
| rs560904045 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311370 | GCGATTTGGGAGGCC[A/G]AGGTAGGCGGATTGC | 10533 |
| rs560910086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11395711 | TTTGGGAGGCCGAAG[C/T]GGGCAGATCACGAGG | 10533 |
| rs560920107 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11400833 | TTCATACATTACAAA[C/T]GTCACTCAGGGTAAT | 10533 |
| rs560925842 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11533076 | AGAGACAGAGCAGCC[C/T]GGAGGTGCGCTGGTG | 10533 |
| rs560933904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11414780 | ATAAATGACTGTTCA[A/G]TTTTGTAAAATGTTC | 10533 |
| rs560949493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486652 | CAGTTTTTGCCCATT[C/T]AGTATGATATTGGCT | 10533 |
| rs560961422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436014 | CTGGGGTGAGTGTAT[C/T]GTTTGAGCCCAGGAG | 10533 |
| rs560962959 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352932 | TTCCAGGGAAGAAAA[C/T]TGGCCTTTTGAAGGT | 10533 |
| rs560977740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481138 | CATGTGCTTTGTGCA[C/G]AGCACTGTGTAAGCA | 10533 |
| rs560978834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333655 | GTGTGTATATATATA[C/T]ACACATATATATATT | 10533 |
| rs560980172 | in-del | -/GA | 0.0887219 | 0.191022 | intron-variant | ATG7 | GRCh38.p7 | 3:11441367 | CTACCTCAACCTCCC[-/GA]ATAGCTGGGATTACA | 10533 |
| rs561002741 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11283647 | ACCATTAAAAACTCT[C/T]CTGCTTGTGGTGGAC | 10533 |
| rs561006927 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11382008 | GTATAATACATGTTA[A/T]ACAGAGTCATGTCAT | 10533 |
| rs561010626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313059 | TTCTGTTAGCAAGTG[G/T]TCAATAAAGTATATT | 10533 |
| rs561016281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11511067 | AAGCTGCAGACCTTC[A/G]CGGTGAGTGTTACAG | 10533 |
| rs561020218 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473359 | ATACCAACAGGACTT[C/T]CCTGCAAATCATCCC | 10533 |
| rs561040363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11376863 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10533 |
| rs561041427 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11409021 | TATTGTTGTGTTCTA[A/G]GAGTTCTTCATGTAT | 10533 |
| rs561046440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370322 | CAGCTTAGTTTTTCT[C/G]CCCCCTTGGTGACTC | 10533 |
| rs561051703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306704 | TCTCTTTGGGGGACA[A/G]TAGAACAGCATCCTG | 10533 |
| rs561054733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546378 | GGTTTTGCCATGTTG[A/G]CCAAGCTGGTCTCGA | 10533 |
| rs561067584 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11528742 | AGGCAGGAGAATCAC[-/T]TTGAACCCAGGAGGC | 10533 |
| rs561084502 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11469915 | GAATCTCTTGAACCT[A/G]GGAGGCGGAGGTTGC | 10533 |
| rs561106227 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11529606 | TTATCAGCAACGTGA[A/G]GTTTGTCCCTGTGAC | 10533 |
| rs561120327 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11311858 | GCAGAATTAGAGACC[A/G]CAGAGATTACAATTA | 10533 |
| rs561129635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334440 | AGTAGAGACAGGTTT[C/T]ACCATGTTGGTCAGG | 10533 |
| rs561144329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11291304 | CAGGGCCTTTTTGTT[C/T]TGACTGTTGGAGAGG | 10533 |
| rs561146520 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11515882 | AGCAGTGCTGTGGGG[A/C]TTGAAGCCAGCATGA | 10533 |
| rs561152097 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11546888 | GCCCACCCTTGCCAG[A/C/T]GGAGAGCAGCACAGG | 10533 |
| rs561153310 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400639 | ACTGCTTGAGTCAAA[C/T]CAAACCTGTACCTGG | 10533 |
| rs561171971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517554 | GCTGAGATGGAGAAT[C/T]GATGCTCAGATTCTT | 10533 |
| rs561176798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284286 | GGGAGAATGGTTGGG[C/T]GGTCTCACTCCAGGA | 10533 |
| rs561181192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290635 | GCTTCAGACGCACAA[A/C]CTTGAAGGCACCAGG | 10533 |
| rs561192348 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11554737 | TGCCATGACTGCTGC[A/G]GTTTTGAAGCATCTG | 10533 |
| rs561194592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301779 | CATCAACAGTCTGTT[G/T]TGTGTAATCTGGAGA | 10533 |
| rs561195891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11407699 | AGGCTCAAAACCACG[C/T]GGAAGCTGTCAAGTC | 10533 |
| rs561196412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292539 | TGCTAGGATTACAGG[C/T]GTGAGCCACCACACC | 10533 |
| rs561200387 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397456 | CAAGAACTACCAGAA[A/G]TAAATGATTTTTCCC | 10533 |
| rs561211374 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11487624 | TCCCGGACGGCACGG[A/C]TGGCCAGGCGGGGGT | 10533 |
| rs561215544 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11396266 | AGGCTTGCCAACACA[C/G]TGAAACCCCATCTTT | 10533 |
| rs561216655 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11436884 | AGTCAAGAAAGTAGA[C/T]TAATGGTTGTCAGCA | 10533 |
| rs561228724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314116 | GCATTCTCCTACCCT[C/T]GTACCAAGTTGCAGA | 10533 |
| rs561243912 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365929 | AAACCACCCATAATA[G/T]AACTTGTGGGCCGGG | 10533 |
| rs561261588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362572 | ATTTTTGGTTAATAT[C/T]CCCCAATCTGTTTAG | 10533 |
| rs561289211 | snp | C/T | 0.000100496 | 0.00708786 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554852 | CATCTGAGATGGCCC[C/T]GCTGTGGGGCTGACT | 10533 |
| rs561300054 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280934 | CATTAATTAATTCAG[C/T]AACCAAGATCCTTTG | 10533 |
| rs561318469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408306 | GACCACCTTAGCCTG[G/T]ACCTTGTTTATATCA | 10533 |
| rs561325325 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11444330 | TCTTTTCATTATCAC[C/T]CCTCCTAGGGGGATA | 10533 |
| rs561332554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11320661 | GTAAGCTCTACCAGG[A/G]CAGGTACCCTATCTT | 10533 |
| rs561336739 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11415417 | TAGCTTACTGTAACC[G/T]TTTTCACTTTATAAA | 10533 |
| rs561339601 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298127 | GAGGTTGTAGTGAGC[C/T]GAGATTGCACCACTG | 10533 |
| rs561349187 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11490281 | GTCTTCTATCAGAGA[C/G]TAGGATTGCAACCCC | 10533 |
| rs561370877 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11321617 | AAAGGAAGCAGCCAT[A/T]TTTTTTCTGCTCAGC | 10533 |
| rs561373486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11314697 | TCCAGCACTTTGGAA[C/T]GCAGAGGTGAGCATA | 10533 |
| rs561374068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273810 | TGTCAGTAAGGGTTG[G/T]TAGGTGTTTCCGATT | 10533 |
| rs561377405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402259 | CAACATGGTGAAACC[C/T]GGTTTCTACTAGAAA | 10533 |
| rs561388218 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG7 | GRCh38.p7 | 3:11405008 | TAAGAATATGCTTCA[A/G]CTTTTCAAAGCCTCC | 10533 |
| rs561408213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498360 | GCAGTCCCCTGTATG[G/T]CACTGCTGCTGAAGA | 10533 |
| rs561424628 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11398220 | AATACATATAGAATA[C/G]TGCACCTAACTGAAA | 10533 |
| rs561434066 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11308645 | CTTTTATTTCTGTAA[A/C]CCTGATGTGCCTGGT | 10533 |
| rs561434684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277023 | CCCTGAGAGTCATCT[C/T]AGACTCTTCCTCTGG | 10533 |
| rs561440651 | in-del | -/TG | 0.0158469 | 0.0875917 | intron-variant | ATG7 | GRCh38.p7 | 3:11497367 | AATACTATATATATA[-/TG]TATATATATATATAT | 10533 |
| rs561446259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379784 | GGAATAAAGGACCTA[A/G]TATAGTTCTTCTGCA | 10533 |
| rs561451294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349231 | CCTCTAGCTAGACAG[A/C]AAAGTTCTCCCAAGT | 10533 |
| rs561469793 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11501036 | AAGGTGCGAGGATCA[C/T]TTGAGGCCAGGAGTT | 10533 |
| rs561471087 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356617 | GGTATTGCATGATTA[C/G/T]ACTTCCATCTTGGTG | 10533 |
| rs561474894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437145 | TCCCTCTCTCCTTTC[C/T]CTGGTTCTCTCTGCA | 10533 |
| rs561480057 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11372904 | GGGGAGAGGGGAGAA[G/T]GAGAAAACAATATTC | 10533 |
| rs561483686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341932 | GTATCAAATCTGTGG[C/G]CCCCTCGTTGCAGAG | 10533 |
| rs561506569 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11411606 | GCCTGGTGACACAGC[A/G]AGACTCTGTCTCCAA | 10533 |
| rs561535038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519974 | TTGGGATCTTACCAC[A/G]GAAATAGCTTTGGGG | 10533 |
| rs561550139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450400 | CAGTTCTCTAGATTT[A/G]TACTTTGGTAGGTCA | 10533 |
| rs561550274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443636 | AAATGATCCACCTGC[C/T]TCAGCCTCCCAAAGT | 10533 |
| rs561550932 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11401080 | AAGTGGTCCGAGCAC[C/T]AGCAGCATCAGTGCC | 10533 |
| rs561554552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430142 | TTGAGCTTATAACCC[A/G]TCTTCAAAAAGGATC | 10533 |
| rs561583704 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11282760 | CTCCCTCTTTAACAG[A/C]CTTGCAGATTGTTTC | 10533 |
| rs561594572 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11352138 | TAATTTGCTCAGAAT[G/T]ATGATTTCCAGCTTC | 10533 |
| rs561596316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418264 | CATATGTCACCATAC[C/T]TGGCTATTTTTTTTT | 10533 |
| rs561596412 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11296439 | TTAAATCAGCCCCAA[C/T]GAGGGTCCCCTCCTT | 10533 |
| rs561596724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304996 | ACCCTTAGCAATTAC[C/T]CTCCATCCCCCCTCC | 10533 |
| rs561600983 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11367181 | CCATTTATGCAACCA[C/T]GTTTTGATTAGGGGA | 10533 |
| rs561604459 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG7 | GRCh38.p7 | 3:11511837 | CGCAGCCACTGGCCC[A/G]GGTGCTAAGTCCCCC | 10533 |
| rs561614135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11348580 | GAAGCCACGGACGTT[C/T]GCATGTTACAGCTCT | 10533 |
| rs561618564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465021 | GCCTTATTAAAGATG[C/T]AGAGAGAAGTCATTG | 10533 |
| rs561646171 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464197 | GGCAACATGGTGAAA[A/C]CCCATCTCTACAAAA | 10533 |
| rs561648224 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338717 | CCACATCAGAGTGCC[C/T]GATTTAAAAGGGGGA | 10533 |
| rs561657650 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11426954 | CAAGCTTTCTGTAGT[A/G]AAGACTGACATGCTT | 10533 |
| rs561657907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11304552 | GTAGATTCCTCCAGG[C/T]ATGATGAGCACAGGT | 10533 |
| rs561663095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11325187 | GTGATGTTGGTATGA[C/T]GGTGAAATTGCCTAA | 10533 |
| rs561669197 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391024 | GGAATAAGAGCTCGT[G/T]TGATGGGTGTCATGT | 10533 |
| rs561686091 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11360886 | TATTTAAATATTATC[C/T]TTTAACAAAGAGAAG | 10533 |
| rs561686289 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11463843 | GTGGGCCCAGCTGGC[C/T]CTCTTGCTCATTTTG | 10533 |
| rs561688388 | in-del | -/AAAAG/AAAG | 0.499759 | 0.0109798 | intron-variant | ATG7 | GRCh38.p7 | 3:11396793 | CTCCAAAAAAAAAAA[-/AAAAG/AAAG]AAAAGAAAAGAAAAG | 10533 |
| rs561692830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11440864 | AGTTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 10533 |
| rs561703757 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11532483 | ATCCCAGTGCTTTGG[C/G]AGGCCAAGGTAGGAG | 10533 |
| rs561722565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317087 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 10533 |
| rs561723369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331090 | GTGTATTTAGCTCCT[A/G]CTTTCTGCCAGGCAC | 10533 |
| rs561726528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490017 | GCAGAGCTGAGTTCA[A/G]TTCCTGGGTATCCTT | 10533 |
| rs561735434 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11406475 | GTGCCCAGTTAACTT[-/A]AAAAAAAAAATTTGT | 10533 |
| rs561737134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426768 | TTGCATTTTAAGTCT[G/T]GAGACTCCTTTTTAA | 10533 |
| rs561744624 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11415527 | TTTTTTCTTTATACC[A/C]TTATCCTATACATTT | 10533 |
| rs561749584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420182 | CTTTTTGTAAGCCAC[G/T]TATAACACAGATTAA | 10533 |
| rs561758512 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413352 | CTTCTATTCCTAGTT[A/T]AAGTGTTTTTATCAT | 10533 |
| rs561767897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11326123 | CAATGTCTTAGGATC[A/G]GTTAGCTGCAGAATT | 10533 |
| rs561768959 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299036 | TTATTTTCTCTTGTT[A/G]TGGGGAAAAAGAAAG | 10533 |
| rs561790007 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11280652 | GAATTTTAGTCACTT[C/G]TATTGCCTGTTTCTT | 10533 |
| rs561808808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538233 | GGCTGGGTGGCACTG[C/T]CCTCTCAACGCTGAC | 10533 |
| rs561827505 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501046 | GATCACTTGAGGCCA[A/G]GAGTTCAAGACCAAC | 10533 |
| rs561831647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11297339 | CTGTAGCCTGGGCAG[C/T]AGAGCGTGACCCTGT | 10533 |
| rs561838371 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526267 | CTAGTGGTGCATGCC[G/T]GTAATCCCAGCTACT | 10533 |
| rs561847439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352519 | CCAGCACCTGTTGTT[G/T]CCTGACTTTTTAATG | 10533 |
| rs561855621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366263 | TAGAGTTCACTTAGC[C/T]TCCCAGAGTCTCAGT | 10533 |
| rs561868577 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11439283 | CATGTTGGCCAGGCT[-/G]GTCTCGAACTCCTTA | 10533 |
| rs561881244 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ATG7 | GRCh38.p7 | 3:11426063 | GGCTATCATGAATAG[C/T]GCTGCTGTGGACACT | 10533 |
| rs561890336 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542531 | CAGATGTACCTTGCC[A/T]TGGGCCATGGCCCTT | 10533 |
| rs561894858 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11302679 | TTCCTCTGTGTCTTG[A/G]TAACAGAATGTGCTA | 10533 |
| rs561895865 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11362065 | CTGTTATGGTGTTAT[-/A]AATATATAGCTGGTC | 10533 |
| rs561919989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447760 | CCAGGCCTGGGTCAC[A/G]TGCCATCTCTGGACA | 10533 |
| rs561928069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534721 | CCACAGTGGGACGCT[C/G]CTCCCTCCCAGCGCA | 10533 |
| rs561931118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555986 | TTCAGCTCATGGGAG[C/G]TTCATGGGGACACAG | 10533 |
| rs561934456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509218 | TTTTAGCTTATAAAC[A/G]TAGAGTTTGAAAAGC | 10533 |
| rs561938634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452737 | CTGGTTAGGATTGGG[G/T]AACTGAGGGTTAGAG | 10533 |
| rs561943411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319170 | TGCCGGGGGCAGGGC[C/T]GAACCCTAGAGAAAT | 10533 |
| rs561950031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11446289 | CCATTTCAACATTCT[A/G]TGATAACGATAGAAT | 10533 |
| rs561955202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544909 | GCAGCACGCAGTCCC[C/G]TGGGGAAGTCAGATG | 10533 |
| rs561976863 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11502639 | TTGTTGGACATTTGG[A/G]TTGGTTCCAAGTCTT | 10533 |
| rs561981457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484325 | CTTGAACCCAGGAGG[C/T]GGAGGCTGCAGTGAG | 10533 |
| rs561983220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281821 | AGAAAAATCAAACAT[C/T]TTGAAAATCGGAAAT | 10533 |
| rs561995892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338556 | ATGGTGGCTCATGCC[C/T]GTAATCCTAGCTGCT | 10533 |
| rs561997522 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11326448 | GGACTACAGGTGCCC[A/G]CCATCATGCCCGGCT | 10533 |
| rs562012856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11446731 | CAACCTCTAAATCCA[G/T]TCAAGGGGCTACTTG | 10533 |
| rs562013407 | in-del | -/AAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374918 | AAAAAAAAAAAAAAA[-/AAAA]GTCTGGGCATGGTGG | 10533 |
| rs562020011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11288901 | CTATTTCAGTTTAAT[C/T]TTGACTGAACTTCTT | 10533 |
| rs562023432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381170 | GTCAGTAGTTACCCA[C/T]GAGCCCATTCTTTCT | 10533 |
| rs562060465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11359732 | AAAAACAAAAAAAAA[A/C]CAACTATGCGGAGCC | 10533 |
| rs562075327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551471 | TACTCCAGTTTACGT[C/T]TTTCCAGGAGAGATT | 10533 |
| rs562085972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11540015 | TTGGAGCTGTTATAA[A/G]TGAAGCTCTGATGAG | 10533 |
| rs562102026 | in-del | -/TA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410344 | TATTTTTTTTTAAAT[-/TA]AAATTTGATAGTATT | 10533 |
| rs562112440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361147 | ATCAATGGCTTGACA[C/T]TGCCTCCCAGGTAGT | 10533 |
| rs562124266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406559 | GCAGTCCTCTTGCCT[C/T]GGCCTCTGTATTAGT | 10533 |
| rs562131425 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11339046 | TCATGCCTGTAATCC[C/T]ACCACTTTGGGAGGC | 10533 |
| rs562133001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430027 | CCTCAGTTCCTTTCC[C/T]GGAGACAAACACTGT | 10533 |
| rs562150186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422917 | GCGCCACTATGCCCA[A/G]CTAATGTTTGTATTT | 10533 |
| rs562164151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11328976 | ATGCCTGTCTGTAGT[C/T]CCAGGAACTAGAGAG | 10533 |
| rs562176869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11472985 | TTTTTCAGGAGCATA[C/T]TTTCCTTTCACTTTT | 10533 |
| rs562179517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312026 | TGAGAAGAGGGGGAA[G/T]GGGGAGTCTCTGCTA | 10533 |
| rs562205872 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11418474 | AAAGAGATTTTTCTC[G/T]AGTATTTACTGAGAG | 10533 |
| rs562208683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551079 | TTCGTAATGAGCCGA[A/G]ATGGCACTCCCCAGG | 10533 |
| rs562210547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413135 | GTTTTACTTCTTCCT[C/T]TTCAATTTGGATGCC | 10533 |
| rs562211871 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389413 | GTTTTATATAATTCT[C/T]TCATTATGAAAGTTT | 10533 |
| rs562216230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328256 | TATGAAATAAGTAAT[A/T]TATTATTTCCTCCAT | 10533 |
| rs562219287 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325409 | AGGCGTGGTGGCTCA[C/G]GCCTGTAATCACAGC | 10533 |
| rs562219402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11523148 | CATCCCTGAGAACAT[C/T]CCCAGGTTGTAAGGA | 10533 |
| rs562225730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11300876 | AAGTGTTCTGGGCAC[A/G]TTTAAGGGAGGCTAG | 10533 |
| rs562237046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433789 | ATTAATATAATTTGC[A/G]TTTTGTCAAGGTTGT | 10533 |
| rs562273804 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464455 | TCCCAGTTGGTTAAC[G/T]CCGCACCCCCTCGGT | 10533 |
| rs562279201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369443 | CCATCCCCTCAACAG[A/G]TAATCTGACTCTGCC | 10533 |
| rs562302173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293346 | ACCAGCCTGTCTAAC[A/G]TGGTGAAACCCCATC | 10533 |
| rs562318000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450550 | AGTGAGTTTTGTCTA[C/T]CATTCTCCATAAGTA | 10533 |
| rs562329915 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390268 | ATCATAAGGCACACA[A/G]ATTTTTTAAAAAGTG | 10533 |
| rs562336774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11422258 | CTTCCACTAGAAGAC[A/G]GTTTCATCTATGTTA | 10533 |
| rs562347760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11492317 | TGCCTCGCCCTGCTT[C/T]GGCTCGCACACGGTG | 10533 |
| rs562350310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406975 | CTTCACATTTCAAAA[C/T]CAATCATGTCTTCCC | 10533 |
| rs562358856 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11277553 | GATGCCGACCCGAGC[C/T]GCAAAACCAGCAGGT | 10533 |
| rs562362426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545579 | TAGGACTTCACGGAC[C/G]AAGCCCTAACCCACA | 10533 |
| rs562365074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335800 | CCTCCTGGGTTCAAG[C/T]GATTCTCCAGACTCA | 10533 |
| rs562373724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11274880 | CTCTAAAATGTGGGG[A/G]CGGGGGTGGAGAGCA | 10533 |
| rs562393615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495968 | TCATAGGCGCGTCAC[A/G]CTAGCATTTCCAGGC | 10533 |
| rs562398860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542002 | TTAAAAATGTGTTTC[A/G]AAGCCTGGAAAAAGG | 10533 |
| rs562400742 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11329551 | TTTTTATCATACAAA[A/G]AACATTCACCGAGTG | 10533 |
| rs562428870 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ATG7 | GRCh38.p7 | 3:11383728 | GCTGAGATTACAGGC[A/G]TGAGCCACCGCATCC | 10533 |
| rs562429817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503195 | GGCCAGATGACCCTA[C/T]ACTGAAGGCCATAGT | 10533 |
| rs562437696 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441493 | ATGATCCACCCACCT[C/T]GGCCTCCGAAAGTGC | 10533 |
| rs562438499 | snp | A/C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11490635 | TTTCCATGTTTAGTG[A/C/G]TTCCTTCAGGAGCTC | 10533 |
| rs562438742 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11553400 | GTTGAATGGGAGAGT[G/T]AAAGAATGGATGGAT | 10533 |
| rs562453172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511203 | CAATGCTGGCTCAGG[C/T]AGCCTGCTTTTATTC | 10533 |
| rs562459131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11468358 | CTTCCCTGGAAGAAC[C/T]GATGGCTTTTTCCAA | 10533 |
| rs562469998 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11437752 | ACAGTTCGCATATAT[A/G]CTTGCTCGTTTTCTC | 10533 |
| rs562474451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542468 | CTCTTGGCAGGTTTC[A/T]TATTTGCTTCTTAGC | 10533 |
| rs562498400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371899 | CCTTTGGAAGCTAAT[C/T]AGACACGCACAGGTG | 10533 |
| rs562499813 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297551 | GAGGGATTATAGAAA[C/G]TTACAGTATACGTAT | 10533 |
| rs562501857 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11511591 | CAGTCCCGTACTGTG[C/T]GCTCACACTCCTCAG | 10533 |
| rs562511315 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11466691 | CTCAGAGGGTTGTAT[G/T]AAGGATTATAGCACC | 10533 |
| rs562511812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350388 | TTACAATTGCAAACA[C/T]TTATTTCATGTTCAT | 10533 |
| rs562515729 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11520832 | AAAAGTCAGCATTTA[G/T]TAGGAGCCACCCCAC | 10533 |
| rs562521320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11475595 | AGACGCGGATGCTAC[C/G]CTCTGCAGTCTGCAG | 10533 |
| rs562546226 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11285167 | TTTTTTTTAAAAGCC[C/T]GGCCTTTTTTTTTTT | 10533 |
| rs562549959 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11523157 | GAACATCCCCAGGTT[A/G]TAAGGATTAGTCAGA | 10533 |
| rs562563440 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11389854 | TCACTGAAGCATTTG[G/T]ATATTTTAAAGAACT | 10533 |
| rs562580894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477342 | CTGAATCGATAAATA[C/T]GTTCAGTAATGAATG | 10533 |
| rs562594016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383326 | TAGAATTTCCCTCCA[C/T]GTGGATTTGTCTGAT | 10533 |
| rs562612216 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11384821 | CAAAAATTGGCCAGG[C/T]GTGGTGGCCTATGCC | 10533 |
| rs562622738 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11292405 | GCTGGGATTACAGGC[A/G]TGCACCACCACACCT | 10533 |
| rs562634587 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367223 | ACGTTTCCACAAAAA[C/G]ACTGGGCTGTGTTGC | 10533 |
| rs562635068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11553757 | CCTCCCCTCAGCCTG[A/G]GAGCTGGGTCCTCAG | 10533 |
| rs562646194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285945 | ACGTCTTTGTGGTCT[C/G]TTTCAGTCTGGGACA | 10533 |
| rs562665430 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408219 | AGGACAAAATGACAC[C/T]AGTCTCTTTGCTAAA | 10533 |
| rs562672372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11357750 | GTACGGTGGCTCATG[C/T]CTGTAATTCCAGCAC | 10533 |
| rs562673039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416396 | TTTATAGAAATAGGC[C/T]TGTTTAGAATTTCCA | 10533 |
| rs562677300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493266 | AGTCAAGTTGCCCCT[C/G]TCTTTGCCATCCAGC | 10533 |
| rs562682109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408915 | ATCTTGCTGGCCAGA[A/G]CATCTTTTCATATGC | 10533 |
| rs562682897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536707 | CTGCCCCGACCCTGC[A/G]GCTCCGACCGGGGCC | 10533 |
| rs562698121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322928 | ACATAGCAGGGCTCT[C/G]TCTCTACAAAAAATT | 10533 |
| rs562722917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537173 | AGAGCTGCCCTCCCT[C/T]CACTCCTGGACGGGC | 10533 |
| rs562738958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11278321 | AATCTTCACAATTTA[C/T]GTTCAGAGATTGAAG | 10533 |
| rs562739440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315577 | GACCACTGCAAAATT[C/G]AAACTTGTTTAGATT | 10533 |
| rs562755703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439316 | TCAAATGATCTGCCC[A/G]TCTCAGCCTCAGAAA | 10533 |
| rs562769191 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11471088 | CAGCCCTTAGTCTCT[G/T]TCCCCTCCAGGCTAC | 10533 |
| rs562772250 | in-del | -/CTTT | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11276982 | TTGCCAATTCCTCTC[-/CTTT]CATTTAGTCATCCAA | 10533 |
| rs562776594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277560 | ACCCGAGCTGCAAAA[C/T]CAGCAGGTTTTTATT | 10533 |
| rs562777634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500545 | CAACAAGAAAATCAA[A/G]ACCAAAATTCTAGGC | 10533 |
| rs562791159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462717 | TGCTGGCTCTAAGAA[C/T]TAACTATCCTCTCGC | 10533 |
| rs562796625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477794 | TCAGTACAGCCTAGA[C/G]GCATTCTCTGTCCAT | 10533 |
| rs562799018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11499041 | AAAAACAGTCCATAG[C/T]AGTTCCATTTATTAA | 10533 |
| rs562834458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371424 | CTGGACCTTCAACCC[A/G]GGGCCCTGGGAGGCC | 10533 |
| rs562834528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11365167 | AGTTGTATGGATTAT[A/G]GATGGTTGCTAGAAA | 10533 |
| rs562839855 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11334330 | ACTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 10533 |
| rs562844685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438752 | GAGGTTTTTCAAGAT[C/G]TAATATGTGAGAGAG | 10533 |
| rs562855721 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11331512 | TTCTATTTGTATCTC[C/T]GTTTTCCTAAATGCA | 10533 |
| rs562886325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11430955 | CAAGAAGCCTAGGGC[A/G]TTCTAGACTGAATAA | 10533 |
| rs562907787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11342805 | CTATTAGAGAACATT[C/G]TTATACTTGTATGTT | 10533 |
| rs562918643 | snp | G/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11398161 | AAAGAAATCGGGAAG[G/T]GTTATTGAACTTGGT | 10533 |
| rs562921870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11336873 | AGACAGGGTTTCACT[A/G]TGTTGCCCAGGCTGG | 10533 |
| rs562922889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403407 | TAAGAGGGATTATGT[C/T]TAAAATGGTAATTGT | 10533 |
| rs562923342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485097 | TGGTATTTCTAGTTC[A/T]AGGTCCCTGAGGAAT | 10533 |
| rs562944924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308759 | CTGCTGAGAGGAGGC[A/G]CCTGGGTTCCCTCAC | 10533 |
| rs562958952 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11392892 | AAGTCAAGTCTCAGA[C/T]TAAATTTTGCCACAG | 10533 |
| rs562960339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11549755 | TTTGGAGTAAACAGG[A/G]GTGGAATGGCTGGAT | 10533 |
| rs562974847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11507625 | GAAATGCTAAAGTTA[C/T]GGGTGTTTTTTGTTT | 10533 |
| rs562974881 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11275236 | AAATTCTTTGACTAG[A/T]GTCTCTAATAGATTA | 10533 |
| rs562984683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11480086 | GTGCCCGCCACCATG[C/T]TCAGCTAATTTTTTT | 10533 |
| rs562995082 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326203 | GGCCATTTTCTAATT[A/G]TAAGCTGTTTCAATG | 10533 |
| rs563026210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391965 | GTACTTATTGGGGGG[G/T]GGGTAATTTCACTTT | 10533 |
| rs563029068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11453331 | TTCAGAGTAATTCTC[A/G]GGGTAATCCAGAGCC | 10533 |
| rs563032356 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11468894 | GTATTTTTGTAATGT[A/T]TGTAGACTGCACATT | 10533 |
| rs563035144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360106 | GCTGGAGTGCAGTGG[C/T]GGAATCTCGGCTCAC | 10533 |
| rs563038219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444802 | ATGGGAGAAAATTTT[C/T]TCAAACTATGCATCT | 10533 |
| rs563048125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11501987 | ATCCTGGGTTTACTT[C/T]TGATCCCTCTTGAAG | 10533 |
| rs563048386 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11377064 | CCTTTTGTCAGCTAT[A/G]GGGAGTGGGTAAAAA | 10533 |
| rs563060970 | snp | A/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556463 | GGAGTGTCCTCCACC[A/G]AGCCGGTCAGCTGTG | 10533 |
| rs563064660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385090 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAT | 10533 |
| rs563096059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11506953 | TACAGAGTGACAAAG[C/G]CTAGGGACCACTTCA | 10533 |
| rs563140155 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11480593 | GACAAAAAAACCTTA[A/C/T]AATCTGTGCTCACTG | 10533 |
| rs563150521 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11333921 | CCCGGATAATTTTTT[A/G]TATTTTTAGTAGAGA | 10533 |
| rs563158861 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11303638 | CTGCCACTGCACTCC[A/G]GCCTGGGCGACAGAG | 10533 |
| rs563175503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286817 | CCCATGTTGCCCAGG[C/T]TGGTCTCAAACTCCT | 10533 |
| rs563176774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503472 | AACAAAAAAAAGGAT[A/G]TTCAGGCCGGGCGCA | 10533 |
| rs563179887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11294831 | TTTAATAAGTGCTCA[A/G]AGGCCGGGAGCAGTG | 10533 |
| rs563183616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384658 | CTATCATGTTTTCTT[A/G]TTACTTATGAAGCAT | 10533 |
| rs563185315 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11305634 | TCCTCATCTCACCTG[G/T]ATGAAAAATATTCTT | 10533 |
| rs563191870 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11497402 | ATATATTTAGCCAGG[A/C]ATGGTGGTGGGTGCC | 10533 |
| rs563194481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534252 | GAGTCTTAGCACTGT[A/G]CCCTTCTGCCGCAAG | 10533 |
| rs563200894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480501 | TTGCGGCAGGGGGCC[A/G]AGGCTGTAGTGAGCC | 10533 |
| rs563203969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491094 | TTCCATTTTCCCCGT[C/T]ACTTTCAGGTACAGC | 10533 |
| rs563206238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511946 | TGGCCTGCAAGCGCC[A/G]CATGCAGCCCTGGTT | 10533 |
| rs563207146 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530916 | CCCCTGGGAGGCAGA[A/G]GTTGCAGTGAGCCAA | 10533 |
| rs563226664 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11471362 | ACTTGGGTTCTGCCC[C/G]ACACCTGTCACCTGA | 10533 |
| rs563242987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388549 | TTCTCCTGCCTCAGC[G/T]TCCCAAGTAGCTGGG | 10533 |
| rs563250855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11400192 | AATTAGTAGAGGTAA[C/G]CTGCTGGTAGATCAT | 10533 |
| rs563277260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11491542 | CTTTGGAGGAGGAGA[C/G]GCGCTCTGCTTTTTA | 10533 |
| rs563278957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11447741 | AGATAAGGACTGTGA[C/T]TGGCCAGGCCTGGGT | 10533 |
| rs563302500 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556639 | CCGAACAACAAAAAA[A/C]ATGAATGATTACAAT | 10533 |
| rs563312642 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11442121 | TCTCTTTCTTTCAAC[C/G]GTAACCTGTGGAAAT | 10533 |
| rs563317324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306014 | ATCTGTAAACTCTGA[A/T]ATGCAAGTTAATCAT | 10533 |
| rs563323510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11406427 | CCTGCCTCAGTCCCC[A/C]ACCAAGTTACTGAGA | 10533 |
| rs563334391 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285009 | CCGCCACCATGCCCA[G/T]CTAATTTTTTTTTTG | 10533 |
| rs563335310 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11376355 | CTCAAACCCGTTATG[A/G]ATTTTAAACTCCAAA | 10533 |
| rs563338548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420879 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGACT | 10533 |
| rs563339101 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11506419 | ACAGCACAGATAAAA[C/T]ATTTCCATCATTGGT | 10533 |
| rs563343908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11311476 | AGCTGTGCATGGCAG[C/T]CTGTAGTCCCAACTA | 10533 |
| rs563345321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11400700 | TCAACAGCCATGCAG[A/G]TTGGAGAGAGAGAAT | 10533 |
| rs563346482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498291 | AATCTTCCCAGCACA[A/C]TCAAGGGACACAATT | 10533 |
| rs563358137 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11546118 | TCCAGCCTGGGTGAC[-/AG]AGTGAGGCCCTGTCT | 10533 |
| rs563364821 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11399296 | GAGGTTGCAGTGAGC[C/T]GAGATGGTGCCACTC | 10533 |
| rs563367808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11319061 | CGTCCTCAACATTTA[A/G]TGCAATGCTGGACAC | 10533 |
| rs563373244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466981 | CAAATACAAAAAATT[A/C]GGTGTGGTGGCGGGC | 10533 |
| rs563389981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368767 | AGGAATCAAGGTGAC[A/G]CTACAACAGTTGTCC | 10533 |
| rs563399292 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11420354 | AGGAGGCCTTTTTTT[G/T]TTTTTTTCATTCTGC | 10533 |
| rs563411818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11276338 | GCTTGAGATCCCATC[A/G]CCTCCTTTGCCTCAA | 10533 |
| rs563415299 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11509532 | AATTGTTTGTATTTT[A/G]TGAGCGTTTATAATG | 10533 |
| rs563415421 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557300 | TGCCTTGGCCCCAGC[A/G]TACGAGGAAGCGTAT | 10533 |
| rs563417122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289802 | TGGGCTCAAGCGATC[C/T]TCCTGCCTCAGCCTC | 10533 |
| rs563417332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298064 | TGCGCCTGTAGTCCC[A/G]GCTACTTGGGAGGCT | 10533 |
| rs563418268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11527388 | ACAGGCATGAGCCAC[A/C]ACGCCTGGCCTTTTT | 10533 |
| rs563445584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534620 | TAGTCGCTGTGCTAA[A/G]GGGAGCTGCCACACG | 10533 |
| rs563456362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473909 | AATTTCTGTGCATAC[G/T]TTCAAACCTCAGGTC | 10533 |
| rs563479460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428363 | ATGTAGAAATACCAA[A/T]GTCAGACCCATTGGA | 10533 |
| rs563480714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11339521 | GCAGTGGGAATTCAA[C/T]GAGAAAGGGGGAGTA | 10533 |
| rs563497950 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11328756 | TATAGAACATTTACT[A/C]GCATAGAAGACAGTT | 10533 |
| rs563502319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552603 | GCCAATGGGACGAAG[C/G]CAGTGGAGAGCCCGT | 10533 |
| rs563520560 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11425018 | CCCAGGTTGGAGTGC[A/G]GTGGTGTGATCATAA | 10533 |
| rs563527316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11319870 | ACTGCAGCAGCTTCC[C/T]AACAAGCCTCCTTGT | 10533 |
| rs563527689 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11322136 | TTGTTACTGTGATTG[C/G]TTAATGCTGGAGTTC | 10533 |
| rs563530704 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11472323 | CAATTGGTAGCTCCA[-/G]GCTTACGTCCCCAAG | 10533 |
| rs563532662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510568 | CTCGCTCTTTGTGCA[A/T]CTCGCCGCCCACATC | 10533 |
| rs563537214 | in-del | -/AGAG | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11359189 | AAGAAGAAGGGAGAA[-/AGAG]AGGGAGAGTATGGGA | 10533 |
| rs563537231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492071 | CCAGCCTCGCTGCCA[A/C]CTTGCAGTTTGATCT | 10533 |
| rs563544327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521583 | TTTAAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 10533 |
| rs563551797 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11410065 | CTTTTGCCTCCCTAC[A/G]AAAACTTTACAATCA | 10533 |
| rs563554751 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11306534 | TTCTGGTTTTAGATT[C/G]AAGCTCTGCCTATTA | 10533 |
| rs563561491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11394911 | CAAGAAGAGAAGGTA[C/G]CATAAGTGAGAGTTG | 10533 |
| rs563580023 | in-del | -/GGGA | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11481856 | ATTTATCTGTAAGAT[-/GGGA]GTGAAGGCCAAAGGC | 10533 |
| rs563586823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307930 | CCTGTGGCTTGACTG[C/T]TCCTGGGCCTCCTGC | 10533 |
| rs563590954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11408203 | CACAAATCTCTAGGG[C/T]AGGACAAAATGACAC | 10533 |
| rs563592832 | snp | C/T | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557250 | AGCAAATAATAAATG[C/T]AGTAATAACAGTATA | 10533 |
| rs563592993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313052 | GCACATTTTCTGTTA[A/G]CAAGTGGTCAATAAA | 10533 |
| rs563594866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413999 | TTCATCTAGGTTATG[A/G]TATTAGGTTTGTAAT | 10533 |
| rs563608972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11375464 | GTTAGATACCATTTC[A/G]TACTCACTAGGATGG | 10533 |
| rs563616860 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11469591 | TCACCTGAGGAAGTA[C/T]AGGATGGGAGCTGCA | 10533 |
| rs563652364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11402117 | CAGCAGTTTCACATG[A/G]CTAGCAAAAGGAAAC | 10533 |
| rs563655223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370307 | ACACTGGCTCATGTC[C/T]AGCTTAGTTTTTCTG | 10533 |
| rs563673002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11300073 | GGGACTACAAGCTCA[C/T]GCCATCATGCCTGGC | 10533 |
| rs563675367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414596 | TGTTGAAAAGGAGTG[A/G]TAAGGGGATTTTCTT | 10533 |
| rs563677113 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11405982 | CTTCCTTCCTTGCTT[C/T]TTTTTGTTTTTGTTT | 10533 |
| rs563691159 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411366 | CACGGTGGCTCATGC[A/C]TGTAATCCCAGCACT | 10533 |
| rs563713515 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11538218 | GAGGGCCTCGTGGCA[A/G]GCTGGGTGGCACTGC | 10533 |
| rs563715596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11410139 | GATTGCATTGACTCT[A/G]TAGGTCAAATTGGGA | 10533 |
| rs563731797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334151 | GTTATGTAAATTTCC[C/T]AGCTCACATAAAGCC | 10533 |
| rs563738594 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11320542 | ATCCACCCACCACAG[A/C]CTCCCAAAGTGCTGG | 10533 |
| rs563750421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11410866 | AATAATGCTGTTATG[C/T]ACATGAGTGTACAAC | 10533 |
| rs563760833 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11408666 | TACATGGATGGCAGC[A/G]GGCAAAGAGAGAGCT | 10533 |
| rs563762729 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11368268 | GAAGAAGAAGAAGAA[A/G]GAAAGAAACACTGCT | 10533 |
| rs563767180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421274 | ATTCCTCTGTAGCAT[A/G]CAGTGCTGTTTGATA | 10533 |
| rs563786467 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384076 | TGTATATTATGACTA[C/G]TCCTTCTCTAAAAGG | 10533 |
| rs563800183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11467433 | CCAGGCTGCAGTGCA[A/G]TGGTGCGATCTCGGC | 10533 |
| rs563803789 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11540977 | CAATCTTGGCTCACT[A/G]CAAGCTCCGCCTCCC | 10533 |
| rs563811172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287308 | AAGACAGGCGAGGCA[C/G]CTCTGAGAAGGCTTT | 10533 |
| rs563816915 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11461045 | CATGAGAGAATGGAT[G/T]AATCCAATCTACCAC | 10533 |
| rs563819270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384985 | AGAAGCATGAAATAA[C/T]AAAAAGTCAACTTAG | 10533 |
| rs563825626 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11535952 | CATGTGGGATGACGC[A/G]GCGTTGCCTGCCAAA | 10533 |
| rs563838256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11395801 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 10533 |
| rs563838707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355818 | TAACATATGCCTACC[C/T]TGTGACCCAGAAATT | 10533 |
| rs563843003 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11541044 | AGCTGGGACTACAGG[C/T]GCCCACCACCACACC | 10533 |
| rs563848053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286632 | GTCTGGCTCGATCAC[A/C]TGGGCTGGAGTGCAG | 10533 |
| rs563855171 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11534944 | CCTTTGTGACTTCCT[A/G]GCAGAAGCCTCCACT | 10533 |
| rs563856314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11506848 | TGCTCTGCTGTACAA[A/G]GTCATCCACAGGCCT | 10533 |
| rs563859114 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11443468 | TTGGCTCACTGCAGC[C/G]TCAACCTTCCAAGCT | 10533 |
| rs563875594 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511965 | GCAGCCCTGGTTCCC[A/C/G]CTCGTGCCTCTCCCT | 10533 |
| rs563923840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417674 | TTGATATAATTGGAT[G/T]AATATCTGCCATATT | 10533 |
| rs563925620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11272900 | AAGTTTACTTTCTGA[A/G]AAAGAAGATTCTCGA | 10533 |
| rs563926115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404891 | ATTCAGTTACCTCCT[A/G]TTGGGTCCCTCCCAC | 10533 |
| rs563926187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525643 | CACTGTAAGCTCTGC[C/T]TCCTGGGTTCACACC | 10533 |
| rs563954280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324135 | TTTTCTTCAGTTACG[C/T]TGAGCTTCTTTCTGC | 10533 |
| rs563955916 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539173 | ATGATGTGTACCCTG[C/T]ATCAGGTGCAGTTCT | 10533 |
| rs563957736 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11455449 | ACATTTGGTGGTCCA[C/T]TCATACCTCCTTCAG | 10533 |
| rs563962227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362458 | ATCATTGTTCCTTTC[G/T]GTGTCTCTGTCACTT | 10533 |
| rs563969475 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11380346 | TACTGCTCTTTGTTC[C/T]TCCCCAGAGGGTTCC | 10533 |
| rs563975509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492278 | GGGAACTCCCTGACC[A/C]CTTGCACTTCCCGAG | 10533 |
| rs563977490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11313894 | CATGAGCCACCCTGC[C/G]TGGTCTGTAAAGTCA | 10533 |
| rs563989369 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11381379 | ATACTGAAATCATTT[C/G]GCACAGGTGCCAGGT | 10533 |
| rs564010923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449850 | TGTAGATGGAAAACG[C/T]ATTAACTGCTGAGAA | 10533 |
| rs564014458 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11411452 | AACATGGTGAAACCC[C/T]GTCTCTAAAAATACA | 10533 |
| rs564014564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404125 | TTATTAACCAGCTCA[A/G]TTTTTTTTTTTTTTT | 10533 |
| rs564038085 | in-del | -/ACAGAGTGCTGATTGGTGTGTTTTT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349097 | GTCCTCTAGCTAGAC[-/ACAGAGTGCTGATTGGTGTGTTTTT]ACAGAGTGCTGATTG | 10533 |
| rs564041906 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11457806 | TGAACACCTAAGAGA[C/G]TGTGCAGTGGTAGCG | 10533 |
| rs564054950 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386027 | CCGAGCTTTTTAGGG[A/T]GTTTCCTAGCCTAAG | 10533 |
| rs564055061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529586 | ATACTTGGAAGTATA[C/T]GATGTTATCAGCAAC | 10533 |
| rs564074958 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448441 | TCTCTCAGCCCAGAT[A/G]GCCAGGCTCAGTGAC | 10533 |
| rs564076224 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11373490 | CCACCTGGAGCTCTT[A/G]TTAAACCTGCAGATT | 10533 |
| rs564090123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532447 | GGCTTCTCAGGCTGG[A/G]TGCAGTGCCTCATGC | 10533 |
| rs564096882 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11320428 | GAGTAGCTGAGATTA[C/T]AGGCATACGCCACCA | 10533 |
| rs564097703 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351838 | TCCTTATATGCTTGA[C/T]TTAGTATAGTTTCTT | 10533 |
| rs564105719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323741 | GCAACAATTTATATG[C/T]TGTTAGTTGGGCTCT | 10533 |
| rs564106796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549929 | GCTCTCCGAGGAGGT[A/G]GGGTGCACTGTCTCT | 10533 |
| rs564121519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336783 | GCTCAAACCATCCCC[C/G]CAGCTTAGCTTCCCG | 10533 |
| rs564123813 | snp | A/G | | | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450567 | ATTCTCCATAAGTAC[A/G]TGGGAGACAACTGAT | 10533 |
| rs564131119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11432829 | GACCTTTACTTCCAA[A/G]GCCTTTACTGAGAAT | 10533 |
| rs564132238 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537886 | TGGCTGGTAGAGCCC[A/G/T]GATCCAAAATTGGGA | 10533 |
| rs564151363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398719 | TTGCCAGGTGTTATG[A/G]CACATGCCTGTAGTC | 10533 |
| rs564151491 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11543911 | GGAGGGTGGGCAGGG[G/T]CAAGGGCTGGGGCTG | 10533 |
| rs564152738 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11399599 | CCTTCCTTTTTTGAC[-/AG]AGTCTCACTCTATCG | 10533 |
| rs564160461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549210 | GGATTTCATATAAAT[A/G]AAATATGAAGTATGA | 10533 |
| rs564168476 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11465178 | AAAATGAGCCTGGGC[C/T]GGGCACAGTGGCTCA | 10533 |
| rs564179130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464409 | ATGTATTCAGTAAAT[C/T]TTTTCTAATTGACTT | 10533 |
| rs564180940 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11280052 | ATTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTGAG | 10533 |
| rs564185870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11538212 | ATAACCGAGGGCCTC[A/G]TGGCAGGCTGGGTGG | 10533 |
| rs564191546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11317031 | ATTTTTATTAGAGAT[A/G]GGGTTTCACCGTGTT | 10533 |
| rs564195521 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11494390 | GTAGGCCTGATGGTT[A/G]GTTTTCTGAGAAGGG | 10533 |
| rs564221155 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486392 | ACATTGATTTTGTAT[A/C]CTGAGACTTTGCTGA | 10533 |
| rs564221570 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11304408 | TAGAGGATGTTACAA[A/G]CAGAAACTCTGCGAT | 10533 |
| rs564226139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371971 | GAACAGCCCGGGAGC[A/G]AGGCCAAACAACCAT | 10533 |
| rs564241519 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292304 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGGCACGAT | 10533 |
| rs564242442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11543090 | GCGGCGTCCTCCAAC[C/T]GACCCCACGGTGCAG | 10533 |
| rs564269657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452056 | AAATAGGGAGAGACT[A/G]CTAATGGGTACTGGG | 10533 |
| rs564289857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555920 | TAGGGTAGATTTCAA[A/G]TGAGGCTTCGCTTCT | 10533 |
| rs564293850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11398322 | ATTTGCTGGCATAGA[C/T]GGGATAATTAAACAA | 10533 |
| rs564304383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386494 | GCTTCTCAGATTTGA[A/T]AGGGTTTTAAATCTC | 10533 |
| rs564319386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484244 | ACCAAAAACACAAAA[A/G]TCAGCCAGGTATGGT | 10533 |
| rs564320549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513295 | GCGCCGTGGAGCAGG[G/T]GGCGGTGCTCGTTGG | 10533 |
| rs564322250 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11463418 | TTCAGTCTTGTTGAA[C/T]CAATTGGTTCAGTAC | 10533 |
| rs564332495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392016 | GACTTAATTGGTTAG[C/G]CTCCTTCAGGCTGTC | 10533 |
| rs564359674 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11472119 | TTAGACTCTCACACA[C/G]ATTTAAGCAAACATG | 10533 |
| rs564361985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366079 | AAAAATTAGCTGAGC[G/T]TGATAGTGTGCACCT | 10533 |
| rs564368032 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298150 | CACCACTGCACTCCA[A/G]TGCAACAGAGTGAGA | 10533 |
| rs564383866 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11451784 | TATATGTTTATAGTC[C/T]CAAAAAAAAAAAAAA | 10533 |
| rs564384352 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11290045 | TCCTGGTAGCTGCAG[C/T]CTATAGTATAGACCG | 10533 |
| rs564387226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392609 | TGTCTCTGTAGCTTC[C/G]TGTGGTTTTCCCACT | 10533 |
| rs564410204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11317573 | CCGAAGCCTATGCCC[C/T]TTCTTTCTTTCTTTT | 10533 |
| rs564431267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519859 | AGCCACCATGCCCAG[A/C]CGAGAGGAGTTTTTA | 10533 |
| rs564435705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544267 | CCCTGGGCCTTCACC[C/T]GGCAGCACTTCCCTG | 10533 |
| rs564441340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11296393 | TCATTGCTTGAGTCC[A/C]CCAAGATACCAAGTT | 10533 |
| rs564449942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458704 | AATTCTATGAAAATA[A/G]ACGCACAGGATAAAA | 10533 |
| rs564468968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507853 | TGGACCTGGCAGTTG[C/T]TCACATCCCATCTCA | 10533 |
| rs564471846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344453 | GTCGAGCTTTATCAA[C/T]TACGTTTATCAAGAC | 10533 |
| rs564474892 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11544770 | TTTCTTTTCTGCCCT[A/G]TGGAATCATATCCAG | 10533 |
| rs564494160 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11425146 | TTTTAAGTTTTTTTG[C/T]GGAGACAAGGTCTCA | 10533 |
| rs564499552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11437001 | ATGATGGTTGCACAA[C/T]GGTGATTATACTAAA | 10533 |
| rs564505248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11552755 | GGCACTGCCAGCAGC[C/T]GCATCCCCTCGAGTG | 10533 |
| rs564505498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508426 | ATCCTGGGCCACATG[A/C]GTTAGACAAGCTTGG | 10533 |
| rs564526998 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439172 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10533 |
| rs564529464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478389 | TTGAGAACCAAACAC[C/G]CATTAATGGTGTGGT | 10533 |
| rs564541009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11553352 | AGGTCTACACAGCGT[A/G]TGGCACAGAGCTGGC | 10533 |
| rs564544716 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11539699 | CGTCTTAAGCTATAT[G/T]CGTTTTCTCTTATGA | 10533 |
| rs564547887 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11396048 | CTAGCATGTTTACAC[-/A]AAAAGGACTTTTATT | 10533 |
| rs564553190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334540 | TGAGTCACTGAGCCT[G/T]GCCTCATATATATTA | 10533 |
| rs564584181 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11313589 | ATGTTTGTAAAGTCA[-/T]TTTTTTTGTATATAT | 10533 |
| rs564584992 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555436 | CCAAGGACTGAGTGA[C/G]CTGCTCAGACATGGC | 10533 |
| rs564605918 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11340836 | TAATTCAGCCCAGGG[A/G]GTGCCAGTCATGCTG | 10533 |
| rs564612264 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11413260 | GATCTTAGAGAGAAA[A/G]CGTTCCTTCTTTCAT | 10533 |
| rs564630403 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11422580 | TCTCTGTAGCTCTTT[C/T]ACTTTATTTTTGTGT | 10533 |
| rs564657242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11374615 | TTGTGCTTCAAGAAA[A/G]CACAAAAAGTCCATG | 10533 |
| rs564680989 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492170 | AATCTCCTGGTGCGC[C/T]GTTTTTAAAGCCCAT | 10533 |
| rs564684551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436120 | TCTTACAACTTAATA[A/G]TATAAAGATACAGAA | 10533 |
| rs564690480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370967 | GATTCCTGGCTTTGC[A/C]ACTTGGTAGCTGTGG | 10533 |
| rs564693151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11420818 | TGGAGTGCAATGGCG[C/T]GATCTCGGCTCACTG | 10533 |
| rs564694436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11495216 | ACTCCCCAGGGAAGG[A/T]GGCAGGGATTGTCAT | 10533 |
| rs564695380 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11483389 | CAGATATCCACTGAG[-/CTC]CCAACACGCACAGAT | 10533 |
| rs564701504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274777 | AAATAAAAACTGTAC[A/G]AGGTGATATGTTACT | 10533 |
| rs564707121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11462603 | TGGGATGATGAAAGC[A/G]GAGGAATTTTGCCTC | 10533 |
| rs564708990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455668 | GATTCTGCCCAGACC[A/G]GGGCTGTCTTAACCC | 10533 |
| rs564709562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413103 | ATGTAAAATCATATC[A/G]TTTGCAAGCAGAAAT | 10533 |
| rs564712436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11348494 | AGCTCTTAAAGATGA[C/T]GTGTCTGGAGTTTGT | 10533 |
| rs564721088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533628 | ACGAAAAACTCATTA[A/C]AAACTGCTTCCTGAG | 10533 |
| rs564723450 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341187 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 10533 |
| rs564789443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501925 | GAACTCCTGACCTCA[C/G]TTGATCCCCTGCCTC | 10533 |
| rs564794826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521962 | TGGTATGGCACTCAA[C/G]TCTTTATGCCGTTGG | 10533 |
| rs564810053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11288808 | CTGAGTTTTATTTTC[A/G]TTAAAGTCTGAAATT | 10533 |
| rs564812549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466206 | GTTATACAAGGAAAC[A/G]TGATTACAGTGGATT | 10533 |
| rs564822377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11509060 | CCCCCTTGGGTTGTG[C/T]AGGCCTTTAACTTTT | 10533 |
| rs564848052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11474795 | AGCTGAGATGACCCT[C/T]GTCTAGGCGGAGGGA | 10533 |
| rs564871857 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396171 | ATAACTCTAGGCCAG[A/G]CACAGTGGCTCATGC | 10533 |
| rs564885768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377433 | TTTTCTTCTATTCCT[C/T]GCCACCTGTGGTGGT | 10533 |
| rs564888805 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11516042 | TTTTTAAAAAAAAAA[A/C]AAAACAAAAAAACAT | 10533 |
| rs564898826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356928 | TGAAATCCTTTCTGC[C/G]TCAGGTCCTTTCCTG | 10533 |
| rs564915370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389730 | ATCATTGGAATATAT[A/G]TGCAGCCTCCCACGA | 10533 |
| rs564916878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429541 | TCCCATTTCCAACTT[C/T]GAAAAATCAGATCTG | 10533 |
| rs564918238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488347 | GCTCCTCCAGCCGCT[G/T]CCTCCCGGGCGGCAC | 10533 |
| rs564935916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481238 | AAGTTCTGAGATGGA[A/T]GGTGGTGACGGTTGC | 10533 |
| rs564939046 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11492323 | GCCCTGCTTCGGCTC[A/G]CACACGGTGCTCTGC | 10533 |
| rs564955349 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11427629 | GAGACCAGCCTGGCC[A/G]ACATAGTGAAACCGT | 10533 |
| rs564957345 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11536125 | TGTTTTCTCAGGGCT[C/G]GTCTGTGAGGGGGAG | 10533 |
| rs564977762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11389182 | AGGTTGCAGTGAGTC[A/G]AGATGGTGCCACTGT | 10533 |
| rs564983063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482795 | ATCATTTTTGTACCT[C/T]TTTTTTTTTGAGGTT | 10533 |
| rs564985824 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11554552 | CGAGGTGGACATGCA[-/G]GAGGTGAGCAGAGGC | 10533 |
| rs564992539 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11400650 | CAAACCAAACCTGTA[C/T]CTGGGATATGTCCAG | 10533 |
| rs564998992 | in-del | -/TAAAAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11375039 | AGACCTCATCTCTCT[-/TAAAAA]AAAAAAAAAAAATCA | 10533 |
| rs565004506 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11278897 | AGGGAGTCAGGGAAG[C/G]CTTCCCTCAGAAGTG | 10533 |
| rs565007059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277101 | CTATAGATTCGACTT[C/T]GTTGCTATCTCCTGA | 10533 |
| rs565007339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11299951 | TTTTTTTGAGACAGG[A/T]TCTCACTCTGTCACC | 10533 |
| rs565013360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11376273 | GATGGTTGCAAAACT[C/G]TTCATATACTAAAAA | 10533 |
| rs565014719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11424339 | TTTTAAGAAATATTA[A/G]ATATTCAATGTTAAA | 10533 |
| rs565020431 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11456252 | AATATATGGGCTCTT[G/T]TGACTGGCATCTTCC | 10533 |
| rs565022966 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11442370 | CACAAAGTTGATGTG[C/T]TTTGAAATCTTTAAT | 10533 |
| rs565045871 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11500695 | TCTTGTTACCCAGGC[C/T]GGACGTCTCACTGCA | 10533 |
| rs565050891 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315624 | GATGTTTAAGAACAT[G/T]TCCTTATCTCTATCC | 10533 |
| rs565067086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364513 | TTGCCCTTTGTCCCA[A/G]GGAAATTAGTTTTTT | 10533 |
| rs565080648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11328893 | GGCGTTCGAGACCAA[C/T]CTGGCCAACATGGCG | 10533 |
| rs565089054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11416178 | TAGTTTTCTAGTAAT[A/G]TCTTTATCTGGCTTT | 10533 |
| rs565096189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11498938 | TCTCTGAGTTCAGCT[A/G]TGAGCTCTTGCAGAA | 10533 |
| rs565102710 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11325834 | GTGTCTCTGTAGGAA[C/T]GGCATTTTCTAGATT | 10533 |
| rs565133453 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11281879 | GTACTTCTCCCGTTT[C/T]TCAGGATTCTTTAAA | 10533 |
| rs565150930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284994 | TGGGACTATAGGCGC[C/T]CGCCACCATGCCCAG | 10533 |
| rs565151670 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456036 | TATACAGTTCAATAA[-/T]TTTTTTTTAATATTC | 10533 |
| rs565153523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444721 | AAAATTGACAAATGG[A/G]ATCTAATTAAACTAA | 10533 |
| rs565157999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11383213 | CAAACATTGCATTTA[A/G]TTGTCGTGTCTCTGG | 10533 |
| rs565163790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11528731 | CTCGGGAGGCTGAGG[C/T]AGGAGAATCACTTGA | 10533 |
| rs565167831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11292345 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 10533 |
| rs565176693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384568 | TGTCAGCTGGTAAAT[C/T]GTACTTTGTTTTGGC | 10533 |
| rs565180724 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11285707 | TTGCCTGTTGAACAA[C/T]GTATAAAGCTGTGTG | 10533 |
| rs565183236 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | ATG7 | GRCh38.p7 | 3:11502201 | AAGAACGTTAAATTC[-/T]TTTTTTTTTTTAATT | 10533 |
| rs565189357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284391 | ATGCCAGAAAACTTT[A/G]TGGAAATGATTTCTC | 10533 |
| rs565194867 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430075 | GAGATATTCTTTAGG[G/T]TATATTCTTTATTTA | 10533 |
| rs565198576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322744 | CTCTTTTTCCTCTCC[C/T]TATCCCCTGTAGTTT | 10533 |
| rs565203449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390559 | GACTGTATGTTTCTG[C/T]TGGGCTGTGCTAGTT | 10533 |
| rs565208697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402304 | GGGGTGTAGTGGCAG[A/G]CGCCTGTAATCCCAG | 10533 |
| rs565220552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11422174 | CAAGGGAGTCAGCCT[A/G]TTTTTTGAAGCTTTA | 10533 |
| rs565224543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371369 | AGCGAGTAAAGGGGC[A/C]CAGCGGAGAAGGCAG | 10533 |
| rs565263398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11356008 | TGATACTTAACAATA[C/T]AATGAACCTCAAAAG | 10533 |
| rs565264720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530747 | GCACTTTGGGAGGCT[G/T]AGTCAGGCAGATCAC | 10533 |
| rs565282963 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11349303 | TAGCACTTTGGGAGG[C/T]TAAGGCAGGAGGCTT | 10533 |
| rs565290149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11294568 | TAAAAATTCTTTCAA[A/T]CAATTAAAAGCCAAA | 10533 |
| rs565322311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11308714 | TGTGAAGGCATGAAA[A/G]TGGCCTGGTTGCCCC | 10533 |
| rs565323328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484372 | GTACTCTAGCCCGGA[A/T]GACAGGAGACTCCGT | 10533 |
| rs565357634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390367 | ATTGGAGGAGCAAGA[A/G]TTTCATTTAACAATA | 10533 |
| rs565366291 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293387 | ATATAAAAAATTAGC[C/T]GGGTGCGGTGGTGCA | 10533 |
| rs565366308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11392928 | AACATTAGCAAGCAG[A/G]CACAAAAGTTAGTCA | 10533 |
| rs565378339 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11296058 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 10533 |
| rs565381718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308094 | GCCCCATGCCCCCTC[A/G]GCTTACCGGAAACTG | 10533 |
| rs565391190 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279139 | TGTCATCTAACCCTC[A/C]CTTTCTCAACCATCA | 10533 |
| rs565396650 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11527870 | TAAGATTTTGTTCCA[A/G]AGCAGGTATTTTCAT | 10533 |
| rs565400571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476397 | GCTGCCACCAGTTGA[C/T]CTGAACTTTATGTGG | 10533 |
| rs565404594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11397520 | TGGAGTGCAGTGGTA[C/T]GATCTTGGGTCACTG | 10533 |
| rs565407467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483812 | AGGATGGACTCTACG[A/G]TAGAATTTAAAGAAC | 10533 |
| rs565427081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530347 | GCCTGGCCGTACTCC[A/G]AGAAGCACTCTGCAT | 10533 |
| rs565437479 | in-del | -/CAGAGA | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11547129 | CCCAGAGGGCAGAAT[-/CAGAGA]CTGTCCTTAATCGTC | 10533 |
| rs565437662 | in-del | -/AATG | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556639 | CCGAACAACAAAAAA[-/AATG]AATGATTACAATAGG | 10533 |
| rs565445566 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11554561 | CATGCAGGAGGTGAG[C/G]AGAGGCACATTCCCC | 10533 |
| rs565453905 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379135 | GAGCCTGAGGTTTTT[C/T]AACATAAAATGGGGA | 10533 |
| rs565456732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302872 | GAATTGTATTAGATG[A/T]ATTGTCAGTCAAGTA | 10533 |
| rs565469864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430883 | TTAAAGGATGAGTAG[A/C]CTATTTTTAAAAATA | 10533 |
| rs565480766 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554905 | AGCTCTCCATCGCCA[A/G]AGCAGGACTGCTGAC | 10533 |
| rs565499901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418846 | CAATTATGGTGGAAG[A/G]GGAAGCAAGGCACTT | 10533 |
| rs565517574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519720 | GCCCGTCACCGCGCC[C/T]GGCTAATTTTTTTTG | 10533 |
| rs565517633 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11338886 | TCAGTACCTTCTAGG[A/T]CCCGTAATTATATTG | 10533 |
| rs565519392 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11317457 | CTTGATCTTTTTATG[A/G]TAAGTCTGTGAAACA | 10533 |
| rs565523765 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11503118 | GGAGAGTGGGCAGTC[-/CTT]CTCCAGAGCCTCTGA | 10533 |
| rs565530885 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385308 | GCTGGGATTACAGGC[G/T]TGAGCCACTGCGCTC | 10533 |
| rs565531084 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279378 | GGGTTAAGGGTTTCT[A/G]TAGGATATTCTTAAA | 10533 |
| rs565547081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11527824 | TTTCAGATGTCTTTT[C/T]TATTTCAGATGTTGT | 10533 |
| rs565551377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302016 | TGTGATCCTGCAGCT[A/G]TGACTTTCACACAAA | 10533 |
| rs565558418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309161 | TCTCCGAAGCTACTA[C/T]CTTCTGTTACTTAAA | 10533 |
| rs565561950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419585 | AAACACACTACAAAC[C/T]CATTTTGCTTCTCAT | 10533 |
| rs565563806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11412208 | AAATAAAAACTAGAG[A/G]GGGGTAAGGAAGCAT | 10533 |
| rs565588239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293592 | GTGGCTCACATCTGT[A/G]ATCCCAGCACTTTGG | 10533 |
| rs565589470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478536 | CACGTTTTTAGCCAC[G/T]ATCTCTGACTATTAA | 10533 |
| rs565605439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11411119 | GTTATTTTTCTTTTT[C/T]GTTGTAAAATAGTAG | 10533 |
| rs565606181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438480 | CTGAGGTGGGAGGAT[C/T]GCTTGAACCCGGGAG | 10533 |
| rs565616829 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11503101 | CAAATACCTTCCAGG[C/G]AGGAGAGTGGGCAGT | 10533 |
| rs565617088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11296567 | CGGAATCATATTTAC[C/T]ATGCAGGACTGCCAC | 10533 |
| rs565624936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431760 | ATTACAATTTTCCAT[A/C]TTCTTTGCACCTGTG | 10533 |
| rs565627463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358705 | TCCCCAGGGCAGAGA[G/T]GTGGTTTGTGTGACC | 10533 |
| rs565632423 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498839 | GTGCTCCTTCTCTCT[C/G]AACTCCTGAAATGGC | 10533 |
| rs565641281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11513458 | ACTGCTGGGGGACCC[A/C]GCGCACCCTCTGCAG | 10533 |
| rs565641899 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11303869 | CACGAGGTCAGGGAT[C/T]GAGACCATCCTGGTT | 10533 |
| rs565643058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11277604 | GGGGAGGGGGTGTGC[A/G]AACAGGGAGTGGGTC | 10533 |
| rs565643097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11508110 | TTTTTCAAAAATGTG[C/T]TGTTTACTCTCCGAC | 10533 |
| rs565650182 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11420984 | ATGGTCTCAATCTCC[C/T]GACCTCGTGATCCGC | 10533 |
| rs565652000 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11552913 | TAAAATGGGTAACAC[A/C]TCCCTGAAAGTTTCT | 10533 |
| rs565652252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478215 | TTTTCAAAAATGAGT[A/G]TGAAAATCTAAAGTA | 10533 |
| rs565654852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344085 | AGAGATATTTTCTCC[C/T]GTTAAACTTTCCAGT | 10533 |
| rs565714642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11331649 | TGATCATTCTGTGCT[A/G]AAGATGTTTTAGTGT | 10533 |
| rs565718419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555599 | GATGGGGCTCCTCCC[C/T]GCCCTTATGAGCAGG | 10533 |
| rs565718435 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501674 | ATATTCTGAGGTTAA[A/G]TATCATGATGTCTGC | 10533 |
| rs565728166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11525405 | TCCCTCTTTAGCCTG[A/C]ATGATTAACTTTACT | 10533 |
| rs565729428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11318718 | GTCCACCACTAGCCT[C/T]ATTTAATATTTCCCA | 10533 |
| rs565756407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11376736 | GCCTTATTTATTATT[C/T]ATATTTTATTTTTAT | 10533 |
| rs565758314 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11404277 | AGTAGCTGGGATTAC[A/G]GGTGCTCGCCACCAT | 10533 |
| rs565760005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534437 | TCCTCACATCTTCTG[C/T]TCACAGGCAGGTCCT | 10533 |
| rs565760307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11526701 | ACAATAGTTTATACT[C/G]TTGTTGTCTGTGTAC | 10533 |
| rs565767181 | snp | A/G/T | 0.00954894 | 0.0685458 | intron-variant | ATG7 | GRCh38.p7 | 3:11502064 | TTTATATATATGTTT[A/G/T]CTGTCATGTAAAATA | 10533 |
| rs565767198 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11459498 | AAACAGGAGCCAAGT[-/G]TTTTTTTTTTTTTAA | 10533 |
| rs565783970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281260 | AGGTATCATGGGTGC[A/C]TTTTTGTAATGACAG | 10533 |
| rs565794779 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304102 | TCTCAAAAAGAAAAA[A/G]ATGTTTTTCTTTTCT | 10533 |
| rs565820308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11432423 | ATAAATGCCATTTGC[C/T]TTTGCTAATGTTACA | 10533 |
| rs565826936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426140 | GTATATACACATAGA[G/T]TAGAATTGCTGCATC | 10533 |
| rs565837419 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11445056 | AAAGTCAAACAATAG[-/A]TGCTGGCGAGGTTGT | 10533 |
| rs565839600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543950 | AGACATCAAGGGCAC[C/G]CAAGTCCCTACAGGG | 10533 |
| rs565844559 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11551213 | CACCCTCTCCTCCTC[A/G]GGGGTTTCATGGCGT | 10533 |
| rs565847133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11281955 | GCCTTCATAACTCAG[C/T]CAGCTTTTAGGAAAC | 10533 |
| rs565852336 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478951 | CTACCTGAACACACA[A/T]GGAGAAATAAACTTT | 10533 |
| rs565859624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11501515 | AGGAAATTTAAGTAC[A/G]GACTCCATATTATTA | 10533 |
| rs565871083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412744 | TGGATTTGTATAGAG[A/T]TCACAATGAATCTGT | 10533 |
| rs565871288 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11401883 | TACGGTGATCCTTTT[A/C]TTAGTTTGTTACAGT | 10533 |
| rs565873179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533948 | AAAAAAACTTGGAGC[A/G]CATCTTGAGGCCCAG | 10533 |
| rs565881057 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11289091 | CTTACATTGATGCCT[A/G]TGTTAATTTCTTTCC | 10533 |
| rs565882435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11425410 | AAAATCTATTTCTTG[C/T]ATAATTACTGTTCTG | 10533 |
| rs565888935 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11434405 | TTTTCCCAGAGCCTT[C/G]TGCTAGCTCACTTCC | 10533 |
| rs565914412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465828 | TTTGGCTTCTATAAA[A/G]ATTAAAAACCCAGGG | 10533 |
| rs565923717 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11549824 | CCTCCAAAGTGGTTT[C/T]GCCAGTTTCCATCCC | 10533 |
| rs565934884 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367862 | ATAAAAAGAATGATT[-/A]AAAAAAAATCATTTT | 10533 |
| rs565944936 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11339638 | GCTTTCATTAACATG[A/C]GAAGGTAGCAGGTGT | 10533 |
| rs565950578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399774 | AGACAGAGCTTCACC[A/G]TGTTGGTCAGGCTGG | 10533 |
| rs565950611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11435068 | GATTTTGATTCAAAT[A/G]TACCATGTATAACCA | 10533 |
| rs565957878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11556027 | TGCAGGGCCCGAGTC[C/T]GCCCACCCAGCCTGG | 10533 |
| rs565966076 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11477306 | ATAAAATGTAAATAA[G/T]AATTTTTGTGCTACA | 10533 |
| rs565975247 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557456 | AAAGCAGACAGGGAT[A/G]CAAAAATAAATGATG | 10533 |
| rs565979474 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11483094 | GCAAAATTATCAGCT[A/G]TTGTGGCAAAAAGAA | 10533 |
| rs565991755 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379291 | GCTCCCCCTTTGGTG[C/T]AAGTATAGTATATAC | 10533 |
| rs566000322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11465337 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10533 |
| rs566006808 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11330704 | GACAGAAAATGAAAA[A/G]TGTTATATACAAGGT | 10533 |
| rs566032136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360417 | GTCTTTTGTAATTAA[G/T]AAGCCCTCAGTAGTG | 10533 |
| rs566034564 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11386937 | CTCTTCACTGCCTTG[-/A]AAAACCTTGGACATT | 10533 |
| rs566038516 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11427862 | AAATGCTCGCTGTTC[C/T]TAGAAAAGGGAATGC | 10533 |
| rs566060297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496014 | GCCCTATGACGTAAG[G/T]AAATTTGGGCATGCT | 10533 |
| rs566067903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11345484 | ACTTTTACAGATGTT[C/T]CTGTGTTGACTCACC | 10533 |
| rs566073200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11490914 | TTAACATTTTTTCCT[G/T]CATTTCAACTTTGGT | 10533 |
| rs566074226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11441872 | GGTTTCACCATGTTG[A/G]CCAAGCTGGTCTTGA | 10533 |
| rs566087495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11491361 | TATTGGTTATTCTAG[C/T]TATACATTCGTCTAA | 10533 |
| rs566087541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484884 | GAACTCATCATTTTT[A/T]ATGGCTGCATAGTAT | 10533 |
| rs566093142 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11533013 | CACAGACAGGGTGGC[A/G]AGGAGAAGCAAGCCC | 10533 |
| rs566102808 | in-del | -/CCCA | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11368820 | GCATTCCTGCTTTAT[-/CCCA]CTTGTGGACCAAGCA | 10533 |
| rs566109655 | snp | C/G | | | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557022 | GGGTCATACGGTGTG[C/G]AGAGTCCACAAAGCC | 10533 |
| rs566124530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11322147 | ATTGCTTAATGCTGG[A/T]GTTCTTTGTCATTTA | 10533 |
| rs566137194 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11439070 | CTTTTCTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 10533 |
| rs566139973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274980 | GTGATTACACTGGAC[A/G]GAAAAAGACAAGCAG | 10533 |
| rs566141858 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11374014 | ATCACTGTGCTATGA[G/T]TAAATACAAGTAAAT | 10533 |
| rs566145265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11387482 | GACCAGAAAGTTGAG[A/G]GCTGTGTTCTCCTTA | 10533 |
| rs566157982 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11427444 | AGTTATGCTTTGTTT[A/C]TCAGCTAAAATATTT | 10533 |
| rs566163300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450243 | AGAGCCAAGTCGTTT[A/G]GCTCCAGAGCCTGTG | 10533 |
| rs566175105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458881 | CGCCTGTGCTCTGCC[G/T]CCTGTCAGATCAGCG | 10533 |
| rs566190684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11473459 | AGGCTAAAGGGAGGA[C/T]AAATAATTTGCCAAA | 10533 |
| rs566191483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368488 | GGCTGTACCTCCTCA[A/G]AGGATGATAATGAGG | 10533 |
| rs566236610 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349846 | CTTTTTGCTCTAGCT[G/T]CTTCTGGTTTTTGAG | 10533 |
| rs566237616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11346266 | AGCATTAACATTGTT[G/T]CCAGTTTTTTACAAT | 10533 |
| rs566247833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11521697 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACGCC | 10533 |
| rs566257853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11536392 | CAGCCTTGGGCTACC[A/G]GCTCCACCTGGCCAG | 10533 |
| rs566258094 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414081 | TGTTTTGTTTTGTTT[C/T]GTTTTTGACATGGAG | 10533 |
| rs566260821 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11534909 | GGCGCAGCCCTGCTG[C/T]GGAGGCGCCTCTGCC | 10533 |
| rs566263879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415888 | TATATATAATTGTAC[C/G]TGGTACACTTTTATG | 10533 |
| rs566266564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11394476 | AGCCGTAGTATTAGG[G/T]CAATTTTTTGTTTTA | 10533 |
| rs566290089 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345340 | CGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 10533 |
| rs566294418 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363994 | CTCTGACAGGAAGTA[C/T]TTGGGATAAAATCTT | 10533 |
| rs566305801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298241 | ACAGGCCAATTAGGA[C/T]GGTTTTCAAAGTTGT | 10533 |
| rs566306193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480599 | AAAACCTTACAATCT[C/G]TGCTCACTGGTTTCC | 10533 |
| rs566319514 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11474408 | AGTTCGAGACCAGCC[C/T]GGGCAACATGGTGAG | 10533 |
| rs566322225 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11343451 | TGTTCTTTGGGTTGT[A/G]TCTTTTATTGATTTA | 10533 |
| rs566327883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393831 | GAATACTGGTGCATG[A/C]CACCACACCAGGCTA | 10533 |
| rs566331487 | snp | G/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342234 | TGTCAAATGTCTGCT[G/T]CTTGGAGCCGGCACC | 10533 |
| rs566342001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11499090 | TTTCATAGGTAATTA[C/T]GTCCTAACAATTTAG | 10533 |
| rs566342874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11447827 | CAGCCTGGGCCAGGG[A/G]CAGGTCATACTGATT | 10533 |
| rs566346203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485258 | GTGTGAGATATCTCA[C/T]TGTGGTTTTGATTTG | 10533 |
| rs566360158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529922 | ACCCTAGCATGACCC[A/G]TCTGCACCACCATCC | 10533 |
| rs566364715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11361195 | GTTCCCTCTACCTTT[A/G]CAAAATAGGAGTGAT | 10533 |
| rs566367135 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | ATG7 | GRCh38.p7 | 3:11306115 | ACTTTGCTTACTCTG[A/C]GGACTGTGAGGCCTT | 10533 |
| rs566367989 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11492656 | AACTCCCTTAACTTG[A/G]GTCCACTCACTCCAC | 10533 |
| rs566369773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11554153 | CTCCTCACAGCCACG[C/T]TGGGGCCTCCTGCTC | 10533 |
| rs566370447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11541312 | TCTAATTGTTCCAGC[A/G]ATGTTTGTTGAAAAG | 10533 |
| rs566371820 | in-del | -/TTTTA | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11484548 | GATATTTTCTTTTTC[-/TTTTA]TTTTATTATTATTAT | 10533 |
| rs566374529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11456567 | CAATATGATATATTC[C/T]GATACTTAAACCCAT | 10533 |
| rs566381883 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390209 | CTATGTACAATATTT[A/T]CGTTATTTCAGTTTG | 10533 |
| rs566382131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11530505 | GAAATGCAAGAAATG[C/T]AAAGATAAATACAAG | 10533 |
| rs566394178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315637 | ATTTCCTTATCTCTA[A/T]CCTCTCCCACCCCTA | 10533 |
| rs566400879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11329049 | GCAGTGAGCCGAGAT[C/T]GTGCCGCTGCACTCC | 10533 |
| rs566421397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11277633 | TCACAAAGATCACAT[A/G]CTTCTGAGGAAACAG | 10533 |
| rs566424946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444066 | TTTGAATTTTTCAAA[C/T]AGAATTATGCTATAA | 10533 |
| rs566437104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444388 | TTAATACTAAAGAAT[A/C]GGGTTTGTCAGATAG | 10533 |
| rs566458092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285359 | TTTTTTATTTTTTGT[A/G]GAGATGGGGGCCCAC | 10533 |
| rs566459070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11408491 | CAACACCCCATTCCT[A/G]GTACCAGATTACTGG | 10533 |
| rs566466171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11348944 | GAGTGCTGATTGGTG[C/T]GTTTACAATCCTCCA | 10533 |
| rs566471191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11402548 | ACATGGCTGTGGATT[G/T]GACCTAGGTTTCACC | 10533 |
| rs566471564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542115 | TTGCTAGCCATTCGC[A/G]TCAGCGACAGGAGCC | 10533 |
| rs566472751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492426 | AATCACCCGTCTTCT[A/G]TGTCACTCACGCTGG | 10533 |
| rs566512641 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271367 | CTGGGACTACAGGCG[A/C]CCGCCACCACGCCCG | 10533 |
| rs566516959 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461979 | GAGCTTGCAGTGAGC[C/G/T]GAGATCATGCCGCTG | 10533 |
| rs566525774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11524128 | ATTCTCTGTTCCATC[A/C]AAAGGAACCCCAAAT | 10533 |
| rs566549911 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440355 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 10533 |
| rs566549973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541480 | GTCAGTGGGTCAGTG[C/T]CTGCCTTGTTACTTG | 10533 |
| rs566556976 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11377066 | TTTTGTCAGCTATAG[A/G]GAGTGGGTAAAAAAT | 10533 |
| rs566580403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455856 | GGTTAATTACTTCTC[A/G]AAACTTACCTCAAAT | 10533 |
| rs566590085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11302257 | TCCTCATCTTTAAAA[C/T]GGGTTCTTGCTTTCT | 10533 |
| rs566598179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483238 | GATATCCCCATCCTC[C/T]CTGGTCAGTCTTGGC | 10533 |
| rs566604336 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11356480 | TGAAAGTTGCTGAAT[C/T]CCAGCCTCTTGGGTG | 10533 |
| rs566636676 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11282744 | AGAGAAGGCTTTAAA[A/C]CTCCCTCTTTAACAG | 10533 |
| rs566645837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11482982 | CTAATGATAACTACA[A/G]TTCTGACCTCTATCA | 10533 |
| rs566651523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364796 | AAGCATGTGGGGTCT[C/G]TTTGCCATTCCATCT | 10533 |
| rs566655310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11308829 | CAGTGTGAAGTCGGC[A/G]GAGTGAGGTAACAAC | 10533 |
| rs566664473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11397030 | TAAAGGAAGAAAAAA[A/G]CAAGTACAAGATACA | 10533 |
| rs566676835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366394 | CCCCCACACACAAGG[C/T]GGCATTTTTTTTTGA | 10533 |
| rs566701611 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11390792 | GGCTTAAAATGGCAC[A/T]TGGGTGTGAACAAAT | 10533 |
| rs566704393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11476700 | GCCGAGTATTCTTGT[A/C]CAAAATGAAAATCAG | 10533 |
| rs566726105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11396543 | TAGAAATTTAAGGCC[A/G]AGGTGGGCGGATCAC | 10533 |
| rs566730596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11336489 | TTCCTGTTTTTCATG[C/T]AAATTAATATGTTCC | 10533 |
| rs566731197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11489268 | CTGTCTTTTTGCGTA[A/G]AGGTGTTTGTAGTAT | 10533 |
| rs566748100 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11367493 | CCCACCAGCAACTCA[C/T]TGTGTAATTTGGAGA | 10533 |
| rs566759909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301379 | GGTGAAGAAGTCTTA[C/T]AGGTCTTTCTGGCTT | 10533 |
| rs566765260 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11330209 | AAAAATACTATTTTT[C/T]CTTTGAAAGTAAATC | 10533 |
| rs566774173 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11543407 | CTTCTTGCTCCCATC[C/T]TCCCCCCTGCCTCAG | 10533 |
| rs566784386 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11305288 | GCTAATTAACTTGCA[-/T]TAAGTGCTGATGCTC | 10533 |
| rs566794590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11378646 | GCTGAGATCACACCA[C/G]TGTACTCCAGCCTGG | 10533 |
| rs566801199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372054 | TGTTTTCATTCCCCA[C/T]GGTGAGGACGGTGTG | 10533 |
| rs566810811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11477458 | GTTTTCTCCCTCTAA[C/T]TTATAAATGTCAGCA | 10533 |
| rs566820844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517891 | ACCAGAGTGTTTTTA[A/G]CAGGGTGGTGTGATC | 10533 |
| rs566832892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11469252 | GTCGGGAGTTCAAGA[C/T]CAGCCTGACCAACAT | 10533 |
| rs566838108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372616 | TCCCAGTTCATCTCC[C/G]CACCCTCAGCCCCAG | 10533 |
| rs566838196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11365709 | CTGCCAGCTAGGGCG[A/G]CACTGTCATATTCAG | 10533 |
| rs566855374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384695 | CTAGGCATGGTGGCT[C/T]ACACCTGTAATCCCA | 10533 |
| rs566870083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542809 | AGGTGACGTTTGGAA[C/T]GGCTGAGCATAACCT | 10533 |
| rs566886738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11500161 | CAATAGCAGCAACGC[A/G]CAACATAAAGAACAA | 10533 |
| rs566888487 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11424094 | TAGAGCTCCCCTGCC[-/T]CCCGTCGCCTGGTCC | 10533 |
| rs566919781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286870 | TCAGACCCCCAAAGT[A/G]CTGGGATTGCAGGTG | 10533 |
| rs566920274 | snp | A/C | 0.0558544 | 0.157504 | intron-variant | ATG7 | GRCh38.p7 | 3:11451847 | TCTCTATCTCTCTCT[A/C]TATATATATATACGC | 10533 |
| rs566925047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384116 | AGGCAGCTTCAGGTG[G/T]TCTTTGCAATAATAA | 10533 |
| rs566939972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11391344 | GGTTTAATGTTCCCC[A/G]GAGCATGCACTGATG | 10533 |
| rs566940527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430422 | TGGTCAGTAATAAAA[A/G]CACAGAATTCTGCAT | 10533 |
| rs566947803 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11360180 | CCTCCTGAGTAGCTG[C/T]GACTACTGGCGCAAG | 10533 |
| rs566948243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293725 | GCATGGTGGCTCACG[C/G]CTGTAATCCCAGCTA | 10533 |
| rs566949189 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11494086 | CTGCTGCTTGCCACA[A/C/T]AGAAAGCCAATCACT | 10533 |
| rs566969714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11373907 | TGTGTGGGACCTATT[C/T]TCTCTGTATAGTCCA | 10533 |
| rs566974834 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303637 | CCTGCCACTGCACTC[C/T]GGCCTGGGCGACAGA | 10533 |
| rs566976911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511816 | TGGGGTACTCAGTAC[A/G]CCCTCCGCAGCCACT | 10533 |
| rs566985061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11294910 | ACATGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 10533 |
| rs566988242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11472630 | GGTTATCTTACCTTT[C/T]TTTTTTGTTGCTAAT | 10533 |
| rs567005100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358187 | ACTGAGATCCGTATG[C/T]CTCTGTTTGCTGCCC | 10533 |
| rs567008333 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556856 | AGCCCAGTACAGTGG[C/G]AGTGAAATGTGTGCG | 10533 |
| rs567011030 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11377537 | CTTTACCTGCCCACC[A/T]CCAATGATAAGACAG | 10533 |
| rs567022739 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11349828 | ATTGGGCTGAAAGTT[G/T]AGCTTTTTGCTCTAG | 10533 |
| rs567029167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409818 | CAGTTGCTACAGCAC[A/G]ATTTGTTGAACAGAT | 10533 |
| rs567035649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11363305 | TGGAGTGTAATGGCA[C/T]GATTTTGGCTCACTG | 10533 |
| rs567051053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11448301 | GCTTTTCCTCCTTCC[A/G]GGCTCCTCCATGCTC | 10533 |
| rs567052213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403694 | AAATTAATACGAATG[C/G]TAATGAAAAGGCAAG | 10533 |
| rs567052833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543269 | TGTTCCTGGAACCCC[A/G]GAGCAGTGGGTGTCA | 10533 |
| rs567053819 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391150 | TTACAGCCATAAAAA[A/T]CTTTCCATCTTTAGA | 10533 |
| rs567057279 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434931 | ATGAGTGACCTTGGA[G/T]GAATCCTTCAGTGTC | 10533 |
| rs567059105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457884 | GACTGTGTCTTAGAT[A/G]ATATACCCTCAGGAC | 10533 |
| rs567062826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316617 | GCCATATTAGACTGT[A/G]AGCTCCAAGAGGGCA | 10533 |
| rs567068174 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11412756 | GAGATCACAATGAAT[C/T]TGTAGATTTCCTTGG | 10533 |
| rs567068829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411083 | AAGTCTTTTTTTATC[A/G]TCACATGCTCATCAA | 10533 |
| rs567073797 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11351414 | GAGGGTAGCAGAGCT[A/G]TCTGTGCAAATGCCT | 10533 |
| rs567084350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309546 | CTTGAAAAGGAAATC[G/T]TATTAGGGTAACATG | 10533 |
| rs567085247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369677 | TGTGAGGTCCCAGAA[C/G]AAGAGTCAAGATTGC | 10533 |
| rs567092908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11532111 | TAAGGGACTGTGGGG[C/T]GCTGCAGGGCTGGGG | 10533 |
| rs567101157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11317149 | CTGGCCCAGAGGAAG[C/T]CCTTTTTAAATTGAG | 10533 |
| rs567122581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496930 | AGTGGTGTGATCTCG[C/G]CTCACTGCAACCTCT | 10533 |
| rs567124295 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11551762 | TCTTTTCTTTTTTTT[C/T]TCTCGAGGCAGGGTC | 10533 |
| rs567135896 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11449870 | ACTGCTGAGAACACG[G/T]TTTCATTTTGAGTTG | 10533 |
| rs567149507 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11457543 | GTACCCAGGAGTTCA[A/G]TAAACACTAAATGTG | 10533 |
| rs567159720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451429 | GTTGGCTAGCTGGTC[C/G]TGACCTCCTGGCCTC | 10533 |
| rs567169619 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419930 | ACTTCTCTATTTTGC[A/G]AACTCTCTCAGTACC | 10533 |
| rs567176841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11503069 | CACTAGGATCCAACA[A/G]CACAGGTGGTCAGGC | 10533 |
| rs567179298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11467029 | CTTTGGAGGCTGAGG[C/T]AGGAGAATCACTTGA | 10533 |
| rs567179523 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363818 | GCAAATTAACATGAA[C/T]ATTCTATTTCTTGTG | 10533 |
| rs567195059 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519690 | TCAGCCTCCCGAGTA[C/G]CTGGGACCACAGGCG | 10533 |
| rs567208258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538008 | AGAGGCCAGGGAAAG[G/T]TGGAGGGAAGAGGGC | 10533 |
| rs567210274 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448978 | GAATTAGGGTAAAAA[C/T]GTCACACAAAGTCTG | 10533 |
| rs567221471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387203 | ATGGGAGGGATTGAA[C/T]CAGGGATTTGAAGGC | 10533 |
| rs567222607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289984 | GCTTCTATAAATAAC[A/G]TTTGTACAACAGCAA | 10533 |
| rs567231549 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11339582 | AGAGTGGGATCCACT[A/T]GCAAGATTTACAAGG | 10533 |
| rs567236028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433127 | TGAGCCTCTGTCTCT[A/G]TTTAAGAAAATTAGA | 10533 |
| rs567238019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289310 | CCCCAAATTCCCCTC[C/T]GACCATTACTTCTTA | 10533 |
| rs567242779 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11375573 | TTTTTTTTCCCCTTG[A/C]CCCCAAGATGGAGCC | 10533 |
| rs567258816 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11496171 | CTTTAACTAAAAAAA[A/C]CATCCACAGAGAAAG | 10533 |
| rs567259317 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11539235 | GTCACAACAGCCCTA[C/T]GAGGGAGACAGCATT | 10533 |
| rs567272280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333234 | TGCCAATGCAGACAC[C/T]TACTTCGAACAGAGG | 10533 |
| rs567275899 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11460177 | ACTGGTTCTTTTGGC[A/G]TTGTTTTAAGGTGGC | 10533 |
| rs567278594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11510160 | ACAGAGTTGCCTGAA[A/G]TCATATATCTTTACC | 10533 |
| rs567291657 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11448910 | ACATTTTACACCAGA[C/G]TAATATACTTAAACT | 10533 |
| rs567300862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381485 | TCATTCATTCTTGTT[C/G]TATTTCTAATTAAAT | 10533 |
| rs567303982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401527 | TCCACTACACTCATG[A/G]TATCCACTCACAGCC | 10533 |
| rs567314290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395537 | GAATGATGGTCAGGC[C/T]TACAGTTGACTTGCA | 10533 |
| rs567325354 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11305802 | GTCATTCATTGCACC[A/C/G]CTTCATACCTGTTCT | 10533 |
| rs567332721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11513567 | AGCCCACGCCCACCC[A/G]GAACTCCAGCTGGCC | 10533 |
| rs567332754 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11521194 | CCCTAGGCAGCCATT[A/G]GTTGCCATAGGCAGC | 10533 |
| rs567340193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11441759 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 10533 |
| rs567350403 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417351 | TCATGTATTTTGATG[C/T]ACTGTTGTTAAGTAC | 10533 |
| rs567360904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11388100 | AGCTCTCCTAGATGA[A/G]ACACTAGGATATGAG | 10533 |
| rs567361614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11299561 | CTCATGATTCTCTTA[C/T]ACCTCCCATAGAGAT | 10533 |
| rs567379736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11298139 | AGCCGAGATTGCACC[A/G]CTGCACTCCAGTGCA | 10533 |
| rs567386774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11276420 | TCATTTAAATATTCT[C/G]TGTTTACTCTCATTT | 10533 |
| rs567388461 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11504490 | GGAGAGATTGAAAGG[C/T]ATCCTCAAAACAGTA | 10533 |
| rs567390917 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11498532 | CACTAGGATTAATCT[C/T]CCAAAAACATTGGTT | 10533 |
| rs567392283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401073 | ATTTTCAAAGTGGTC[A/C]GAGCACCAGCAGCAT | 10533 |
| rs567396253 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | ATG7 | GRCh38.p7 | 3:11492123 | AGTGAGACTCCGTGG[G/T]CATAGGACCCTCCGA | 10533 |
| rs567403819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11434232 | TTTAACAACAGTCAG[A/G]TATTTATGTACAGCT | 10533 |
| rs567404917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11459738 | AGGCAATAGCCATTC[A/G]TTCATAATGAAACCA | 10533 |
| rs567411603 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495192 | GGCTCAGTTGGGTAC[A/G]TGGCTTAGACTCCCC | 10533 |
| rs567423129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11483424 | TGCTTTCCTTTTTCT[A/G]TCAAAGTAGGATTAT | 10533 |
| rs567438217 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11303767 | TTGAGGAATATTTGT[C/G]TTTATTCATAAGAAA | 10533 |
| rs567510278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511337 | GTTCTCCATGTTCCC[A/G]TCATATTAGTTAGAT | 10533 |
| rs567515945 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ATG7 | GRCh38.p7 | 3:11295697 | TTTTTACTGCTTAGA[A/G]TTGGTAGATATATGT | 10533 |
| rs567531120 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11401199 | GTTTTAACAAGCCTT[C/T]CTGGGGATTCTGAAG | 10533 |
| rs567532041 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385909 | GTGAGTGCCGTTTTA[A/G]TTTTGGCCATCCTTG | 10533 |
| rs567543222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11415231 | TTTTTTAAAATGGTA[C/T]ACCTGTGCAGAATAC | 10533 |
| rs567555780 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539801 | GAAACGTACTCGCTT[A/G/T]TGGAACCAGCACAGT | 10533 |
| rs567564888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11282940 | TGGTCATGTGGTTTG[A/G]TGCTTATTTTAATGA | 10533 |
| rs567565065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11503497 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10533 |
| rs567567264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460521 | CCATGGCCTAGTTCA[A/G]GATGAGGGCTTGCCT | 10533 |
| rs567567538 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11395904 | GAGGTCACACCACTA[A/T]ACTCCAGCCTGGGCG | 10533 |
| rs567599698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420901 | GCTGGGACTACAGGT[A/G]TATGCCACCTTGTCC | 10533 |
| rs567621147 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11516349 | AATAATAATAAAATT[A/T]AAAAAAAAAAGATGT | 10533 |
| rs567623538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11510948 | CTCGCGGTGAGTGTT[A/G]CAGCTCTTAAGGTGG | 10533 |
| rs567625945 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11306136 | GTGAGGCCTTTGGGG[A/G]CAATGTAGAGTGTGT | 10533 |
| rs567627723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485755 | AGTTTCAGCTTTCTA[C/T]GTATGGCTAGCCAGT | 10533 |
| rs567632448 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11522252 | GCCCTGTGGAAGAGG[A/T]AAGTCACCACGCAGA | 10533 |
| rs567635169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443092 | CTGTTTTGAAATTGA[C/G]TCCTCAAAAGGACAG | 10533 |
| rs567636572 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11486058 | ATGAACTTTTAAGTA[C/G]TTTTTTCCAATTCTG | 10533 |
| rs567639526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551443 | ATGCAGAAACAAGGG[C/G]TGTGGCTCTATCTAC | 10533 |
| rs567695059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11344824 | TAGTGAGCCAAGATC[A/G]TGCCACTGCTCTCCA | 10533 |
| rs567697065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11404178 | TGCTCTGTCGCCCAG[A/C]CCGGAGTGCAGTGGT | 10533 |
| rs567714019 | snp | A/G | 0.000231432 | 0.0107546 | intron-variant | ATG7 | GRCh38.p7 | 3:11380096 | TTTTTAAAAGTGAGC[A/G]GGTCAGCATTTGACC | 10533 |
| rs567720480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11429693 | TGGCTCATGCCTCTA[A/T]TCCTAGCACTTTGGG | 10533 |
| rs567734174 | snp | A/T | | | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270339 | CCTTCTGAATTCCCA[A/T]TCTTTGCCTCATAAA | 10533 |
| rs567736858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11475661 | CAGAACATGGCAAGC[C/T]CCTGAAGGAGAATTT | 10533 |
| rs567748239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362108 | GATTGTCAACAAATA[C/T]GATTAGTGGTCCCTT | 10533 |
| rs567748718 | in-del | -/AAA | | | intron-variant | ATG7 | GRCh38.p7 | 3:11538678 | TGAAACTCCGTCTCT[-/AAA]AAAAAAAAAAAAAAA | 10533 |
| rs567751471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398341 | ATAATTAAACAAGTT[G/T]CAACGAATTTCAGAG | 10533 |
| rs567758577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11448563 | GTAATCAGGAACATA[A/G]ACCAACACAATACAG | 10533 |
| rs567769529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442388 | TGAAATCTTTAATAC[A/G]AACATTTGTTATTGG | 10533 |
| rs567780958 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429482 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 10533 |
| rs567781464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11354370 | TGTCAGATTATGAGG[C/T]CGGGCGCAATTGCTC | 10533 |
| rs567782950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403653 | AGGTGAAGCAGTCTG[G/T]TTCCTTTTTCCTCAC | 10533 |
| rs567785316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529185 | GGCTGACATCCTGGG[G/T]CACCTCCAAAGCCAG | 10533 |
| rs567793223 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11484967 | AGTTGGGTTGGTTCC[-/A]AGTCTTTGCTGTTGT | 10533 |
| rs567799061 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456874 | GCCCCAGTATTGGAG[A/G]CTACTGGATGTGTAA | 10533 |
| rs567817565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421675 | GAATCACGAATACTC[A/G]TATCTAGAATGGTGA | 10533 |
| rs567821536 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11272402 | CGCGCGCCTCAGAGA[A/G]AGCTGTGGTTGCCGG | 10533 |
| rs567848677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11547271 | GTGCTTCAGTCCCCT[A/G]CTTTGTAAAATGGGG | 10533 |
| rs567866376 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11274151 | TGAGTACTGGACTTT[C/G]CATTACTCAACCACA | 10533 |
| rs567872319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424603 | TTTTAATTTTAATAA[A/G]TATTAATTTTTAATA | 10533 |
| rs567893581 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11529423 | CCAGATACGTGGCTT[C/G]AAACAGAGAATTGTT | 10533 |
| rs567897098 | in-del | -/CCTT | 0.00755907 | 0.0610114 | intron-variant | ATG7 | GRCh38.p7 | 3:11399564 | TTCCTTTCCTCCCTC[-/CCTT]CCTTCCTTCCTTCCT | 10533 |
| rs567900298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11468398 | CATGCCTCGCCTATC[C/T]TCCTCCCCACTCCAT | 10533 |
| rs567907511 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271516 | GTGAGCCACCGCGCC[C/G]GGCCTGCAGTAATCC | 10533 |
| rs567916329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389371 | ATGAACTTAATCATA[C/G]TTTTCTAGAGTGTCT | 10533 |
| rs567929536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11330767 | AACTACTTCTGCCAG[A/C]AGAAGTCTTCACTGA | 10533 |
| rs567943250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11525215 | TTTTTATTTTTAGTA[A/G]AGATGTGGTTTTGCC | 10533 |
| rs567944392 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11396894 | AAGAGGTTAAAGATA[A/G]GAATTAATGCTTGAC | 10533 |
| rs567952568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382912 | ACGTATATTTGCTGT[C/T]GTCCTCCAATCCCTC | 10533 |
| rs567953563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11489214 | ACTGCTCTCTTCAAA[G/T]CTGTCAGACAGGGAC | 10533 |
| rs567961508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11309502 | TTTTCTGTAAGCGAA[A/G]TCTAATTAAAATGAA | 10533 |
| rs567973995 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11433354 | CAGTCTAAATCAAAC[A/G]TATGAACACCTTAGC | 10533 |
| rs567986684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303840 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGGTCA | 10533 |
| rs567988494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295274 | AAGCTTATCAATTAT[A/G]TAGAAAAATAATTAT | 10533 |
| rs567993225 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11429028 | ACGAGCCTGAGTTTT[C/G]TTTTTGAATTTTCCT | 10533 |
| rs568017275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519661 | CCCTCCCAGATTCAC[A/G]CCATTCTCCTGCCTC | 10533 |
| rs568017798 | snp | A/T | 0.000183493 | 0.00957668 | intron-variant | ATG7 | GRCh38.p7 | 3:11358643 | AATTATGATTTATGA[A/T]TTAATGCACCACCAC | 10533 |
| rs568023758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11439008 | TATTTTGAGACTGTA[A/C]AATTAAATTGATTTT | 10533 |
| rs568024943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316524 | TGGCCATATATGATC[C/T]ATCCCTATCTGAAGT | 10533 |
| rs568028327 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11335089 | GTCTTTACACAATTC[A/G]CTGAAAGATTGACAG | 10533 |
| rs568032530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11350917 | AACCTAGTTGAGACC[A/C]TAGCCCAAAAAAAAA | 10533 |
| rs568036643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445701 | AAAAAAGAAAATATG[C/T]ATCTTCAATTTTATT | 10533 |
| rs568037803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483353 | TTCTAAGAAGAATCA[C/G]ACTGTGGTTCTTAGA | 10533 |
| rs568053392 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11343155 | GCTGGTCTTGAACTC[C/T]TGCCCTCAAGTGATC | 10533 |
| rs568080038 | snp | C/T | 0 | 0 | intron-variant | ATG7 | GRCh38.p7 | 3:11391773 | TCCCAGTATCCCTTT[C/T]CAGTGTCTTATGAAT | 10533 |
| rs568102351 | in-del | -/CTCT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11486332 | TCACTCATGATTTGG[-/CTCT]CTGTTTGTCTGTTAT | 10533 |
| rs568103798 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11531932 | TGAGTGCTTACTGTG[G/T]GCCAAGCACTGCGCT | 10533 |
| rs568104345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11325452 | CAAGGTGGGCAGATC[A/G]CCTGAGGTCCGGAGT | 10533 |
| rs568114150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287610 | TGCTGCTGATGCAGT[C/T]TTTCCGGAACGTTAT | 10533 |
| rs568117726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537938 | GCTGTTTCCTTTATA[C/T]CCAATGCCACAGAGC | 10533 |
| rs568130949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539168 | CACAGATGATGTGTA[C/T]CCTGCATCAGGTGCA | 10533 |
| rs568135670 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555505 | ATCTGTGCCTGCCTG[C/T]CTGCTTGAGGGAGAG | 10533 |
| rs568142137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11337335 | GTGCGCACCTGTAGT[C/T]GCAGCTACTCAGGAG | 10533 |
| rs568157412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445064 | ACAATAGATGCTGGC[A/G]AGGTTGTGGTGAAAA | 10533 |
| rs568159848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11451296 | GGCTCACTGAAACCT[C/T]GGCCTCCTGGGTACA | 10533 |
| rs568167850 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11286508 | CTTTTGTTTCTTTTC[A/G/T]GGAGGATATCTATAG | 10533 |
| rs568171070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11324914 | ACTATGTACAGTCAC[A/G]TGCCACATGATGTTT | 10533 |
| rs568189387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507978 | CAAAAAAACAAAAAA[C/T]AAAACAAAACTGGGA | 10533 |
| rs568205598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543847 | CTCTGGGGACGGGAG[G/T]GGGAGGACCCATTTC | 10533 |
| rs568219635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11549595 | TAGTTTAATGGCTTA[A/G]GAGTATCCACTGTAC | 10533 |
| rs568233920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11507274 | GAGACAGAGTGAGAC[G/T]CCATCTCAAAATAAA | 10533 |
| rs568237078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11478448 | CTGGCGCATATTAAA[A/G]ATGCCTGCTATGATG | 10533 |
| rs568241270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470790 | GAGCCAGGAGAGGAG[A/T]TGGGATTTAGGCTGA | 10533 |
| rs568243721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11544341 | GGTCCAGCAAGGGAA[A/G]TGGTTAACCCGTGAG | 10533 |
| rs568247923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11418761 | ACTACCTGAAACTGG[G/T]TAATTTATAAAGAAA | 10533 |
| rs568248895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11439593 | GACGCAGTATAGTTG[A/G]GGAGATAGGACAGGA | 10533 |
| rs568255264 | in-del | -/ATG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11293559 | AAAGAAAGAAAGTGA[-/ATG]ATGACTGGCCGGGCG | 10533 |
| rs568262857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337668 | TATTATTTTTTGAGA[A/G]ATGAGGTCTTCTTAT | 10533 |
| rs568263324 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11407975 | GCTCCTAGTTACTTA[A/C]GCAAACTTCTGCAGC | 10533 |
| rs568266934 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11418150 | CACTCTGTTGTCCAG[C/G]CTGGAGTGCAATCGT | 10533 |
| rs568271131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11385509 | GTGTGCCAGAGATAC[A/G]AAGATGATTACAATA | 10533 |
| rs568286060 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11384835 | GTGTGGTGGCCTATG[C/T]CTGTAGTCCCAGCTA | 10533 |
| rs568286524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352738 | TAAAAGGGATAAGTA[C/G]ACATTGCTCAGGAAA | 10533 |
| rs568304755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471422 | AAAATATATGACTTG[A/G]TCATCTTTATACCCT | 10533 |
| rs568306121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11344033 | TAATTGGGTTTAAAT[A/G]TGGTATTTCTGCATA | 10533 |
| rs568306526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11379404 | TGTAGTCCAGAATTT[C/T]ATGCTCAAGGTGGTG | 10533 |
| rs568329574 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11555015 | TGTTCGGCGTTGCTC[A/G]GGATTCAAGATACCA | 10533 |
| rs568341368 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11437257 | TGACAAGGATCTCTT[C/T]CATTTTTATTGTGCC | 10533 |
| rs568346653 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11292080 | GTGTGAGATGATGGA[A/G]CCTGGCACGTAGCAG | 10533 |
| rs568364610 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556220 | AGAGAAGGTCAGAGC[A/G]CACTGCAGGCAGCGC | 10533 |
| rs568368622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405353 | ATGTTCAAGGCTACT[A/G]TGGAGCTTGAGGGGG | 10533 |
| rs568374864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11318638 | CTTCTAAGGTTCCTG[C/T]TGACTTCGGGATAAC | 10533 |
| rs568380347 | snp | A/C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411193 | AGTTCTCTAATTATC[A/C/G]GTGATGTTGAGCATC | 10533 |
| rs568395209 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11383231 | GTCGTGTCTCTGGCT[C/G]CCTTCAATCTGGAAA | 10533 |
| rs568405590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11452944 | GCTGGAAGTGCACGA[C/T]TCCGTGGGCTGTAGC | 10533 |
| rs568417434 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382523 | AGTCACTTTCATTCC[A/G]GTTTCTACTTATTGT | 10533 |
| rs568427006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11326027 | ACATTCTCTAAAGTT[C/G]TATGATTCTGGAGCC | 10533 |
| rs568441117 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11414107 | TGGAGTCTTGCTCTT[G/T]TTGCCCAGGCTGGAG | 10533 |
| rs568447353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11412572 | TGTACTATAGTAAAT[C/T]TGATTACTGTAGCTT | 10533 |
| rs568447872 | in-del | -/CC | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11476130 | GTCCTCTCCTTTGTA[-/CC]CCCTAAGGTGTAGAG | 10533 |
| rs568450439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11352320 | TAAACATATGTGTGC[A/G]TGTGTCTTTATAGCA | 10533 |
| rs568457736 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11417582 | TGATTTTCTTTTAGA[C/T]ACCATATAATTGGGT | 10533 |
| rs568469840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458830 | GTTAGGAACCCGATC[A/G]CGCAGCTGTAGGTGA | 10533 |
| rs568477605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280133 | CTGACTGCAACCTGC[A/G]CCTCCCGGGTTCAAG | 10533 |
| rs568477911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11458510 | CCTCGTGATCCGCCC[C/G]CCTCGGCATCCCAAA | 10533 |
| rs568479844 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512797 | TTGCCATTGCTGGCT[C/T]GGGCAGCCTGCTTTT | 10533 |
| rs568496492 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11331530 | TTTCCTAAATGCATT[A/G]TTTTTTCATTTTGGG | 10533 |
| rs568501948 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452766 | AGAGTAAAGTAGAAG[A/G]GATGGCACTTTTCTT | 10533 |
| rs568505501 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274273 | GGGAATACAAAAATG[A/G/T]GTAAGATACACATCC | 10533 |
| rs568505732 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11323493 | TGGATTCCACAGTCG[C/T]ACTCCATTGCTACAA | 10533 |
| rs568521055 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455589 | TGAGAACAACTGATC[A/G]TGAGCTTGTCCATGT | 10533 |
| rs568523932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353215 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 10533 |
| rs568530653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11541383 | AAGTCACCTGCCCGT[A/G]TTTGTGGGTCTGTTT | 10533 |
| rs568534453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441173 | TCCTACCTTAATCCT[C/T]TTTGAAAGAGGCCAT | 10533 |
| rs568542071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273391 | CTCTTAGGTTGAGCT[G/T]AAAGCAGCTACTCGG | 10533 |
| rs568550793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11484813 | GTTTTTTGTTCTTGC[A/G]ATAGTTTACTGAGAA | 10533 |
| rs568554205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11372794 | CAAAGTTGGTAGGTA[A/G]GGGCTGGGTGTGTGT | 10533 |
| rs568555887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288221 | AATGGAGAACTCATT[A/C]TCTCTCTGATCTATT | 10533 |
| rs568559763 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11541118 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGACT | 10533 |
| rs568563224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479635 | GGAAAAGCTATTGGA[A/T]AGCAATTGTCAAGAG | 10533 |
| rs568566808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11414488 | GGCAGGCATGTCATC[A/T]ATGAACAGACAGTTT | 10533 |
| rs568578536 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11315830 | CTTCCTGGTTCAAGC[A/G]ATTCTCCTGGTCAGC | 10533 |
| rs568604041 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11461955 | GAATGGTTATGAACC[C/T]GGGAGGCAGAGCTTG | 10533 |
| rs568618905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527470 | CCTGTCCCTGGGTAA[C/G]TATTTAATACCATAG | 10533 |
| rs568624328 | in-del | -/T | 0.387589 | 0.208733 | intron-variant | ATG7 | GRCh38.p7 | 3:11390674 | GTGGGTGGGTTTGAT[-/T]TTTTTTTTTTTCCAG | 10533 |
| rs568642621 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG7 | GRCh38.p7 | 3:11541122 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACTTCGT | 10533 |
| rs568644022 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385852 | AGCAGTTGTGGCTGA[A/G]CCTGGGACACCCAAT | 10533 |
| rs568644879 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11517866 | AAGGGCACCACATGC[C/T]GTGGGGAGAACCAGA | 10533 |
| rs568647365 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11442120 | TTCTCTTTCTTTCAA[C/T]GGTAACCTGTGGAAA | 10533 |
| rs568658933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334644 | AATGTGTGTGTGTGT[A/G]ATGGGGGAGGTGGTG | 10533 |
| rs568673983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11305475 | TCTTCCTTCTGTTTC[C/T]ACATCCTGTTTCAGC | 10533 |
| rs568693454 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11345085 | GGTAAAATTCAGTTA[C/T]AAATCCGTCTGGGCC | 10533 |
| rs568730904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11368267 | AGAAGAAGAAGAAGA[A/C]GGAAAGAAACACTGC | 10533 |
| rs568759172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504659 | TTAGGAGGTTTAGAC[A/G]GTTGGCAGAGAGTTT | 10533 |
| rs568768944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11360207 | CAAGCCATCATGCTC[A/G]GCTAATTTTTTGTAT | 10533 |
| rs568775704 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411577 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 10533 |
| rs568785874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461908 | GGTGGCGGGCGCCTG[C/T]AGTCCCAGCTACTCA | 10533 |
| rs568793691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11370401 | CTGAAACAAAGACCA[G/T]TCTGGTGTGCTTAGG | 10533 |
| rs568809120 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11449544 | TACAAAGAAGCTTCT[C/T]ATGTTCCATACAATG | 10533 |
| rs568812498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460722 | ATCCCAGTCAAGGAC[A/G]TATAAATTTTGACAA | 10533 |
| rs568823261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11450083 | TGTAATGGCTAGTCT[C/T]TTGAGAACTTGCTGT | 10533 |
| rs568854894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11321074 | AGTAGGGTGCAGATG[C/T]GTAATGTCTGGGAAT | 10533 |
| rs568886568 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11476570 | ACAAAAAATAAATAG[G/T]GACAAATAGAAGGAG | 10533 |
| rs568905704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11510920 | ACTGACTTCAAGAAT[A/G]AAGCCGCGGACCCTC | 10533 |
| rs568945044 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | ATG7 | GRCh38.p7 | 3:11507953 | ACCTTGCTGGTAATT[A/T]AAAAAAAAACAAAAA | 10533 |
| rs568949860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283854 | GGAGAATCGCTTGAA[C/G]CCGGTAGACGGAGGT | 10533 |
| rs568958765 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ATG7 | GRCh38.p7 | 3:11488421 | TGAACTCCATCCTCC[C/T]GGCGGTCGGGCAGCG | 10533 |
| rs568959505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384016 | CACTCCAGAAAGTTC[C/G]CAGGTACCCTTTCCC | 10533 |
| rs568964145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11421599 | CTCAAAGTCATCCAT[A/G]AGGGTTGGAATCAAC | 10533 |
| rs568966097 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467664 | TACAGGCGTGAGCCA[A/T]TGCGCCTGGCCCTAT | 10533 |
| rs568983795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11504253 | GCAACAATGCTTTCA[A/G]ACAATAAAGGGAAAT | 10533 |
| rs569007257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443941 | CCATCTCATATTTTA[C/T]TTTCTGACCACAGGC | 10533 |
| rs569011605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529328 | AATCCAATAACATTT[A/G]GGAACCGTAACACAA | 10533 |
| rs569017046 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11383514 | GAAACCTGCAATCTC[A/G]GCTCACTGCAACCTC | 10533 |
| rs569021552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486754 | TAGTATGAAGGGTTG[C/T]TGAATTTTGTCAAAG | 10533 |
| rs569051038 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11523024 | GCTTTTCAGAGGTGC[C/G]GATGAAATAGCCTGT | 10533 |
| rs569051055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11355619 | CGTGAAAATGCTCAA[C/T]GTCAATAGTCATCAG | 10533 |
| rs569052593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371025 | TGAGCCTCCTATGTT[A/C]CTATTTGGAGATCTG | 10533 |
| rs569072287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307672 | TACAATATCCTCTCT[G/T]CCTGGAATGTCTTTC | 10533 |
| rs569073916 | in-del | -/GTC | 0.0134861 | 0.0810011 | intron-variant | ATG7 | GRCh38.p7 | 3:11314416 | GATTAAATTTTTTTT[-/GTC]GTTGTTGTTCGTACA | 10533 |
| rs569095081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11314371 | TCATTCAGGGAGCTC[C/T]CTTGGAGCTGTTCAG | 10533 |
| rs569105470 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG7 | GRCh38.p7 | 3:11488813 | GGTTTGCCAGTATTT[C/T]ATTGAGGATTTTTGC | 10533 |
| rs569108159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500105 | TGGAGGTTGGCTTAG[A/G]TGACCTTTTAATTCC | 10533 |
| rs569126390 | snp | A/G/T | 0.000380776 | 0.013793 | synonymous-codon, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11342147 | TAGGTTAGCTGAGTC[A/G/T]TCAGTGGATCTAAAT | 10533 |
| rs569129816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362986 | GTAGGCAGTTGTTCA[C/T]CAGTGTCTCCCATGG | 10533 |
| rs569139732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401772 | CCTGTGTACTCCAGG[C/T]CTACAGACTATAAGC | 10533 |
| rs569149271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11278936 | GCTGTGATTTGAAGT[A/G]AGCAAAGAAATTCAC | 10533 |
| rs569151209 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11272040 | ATCTCCTGGCTCTCC[A/C]CACCTGCCACCCTGA | 10533 |
| rs569155644 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11401780 | CTCCAGGCCTACAGA[C/T]TATAAGCTCTAAGTA | 10533 |
| rs569157615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11469867 | TGGTGGCATGTACCT[A/G]TAATCCCAGCTACTT | 10533 |
| rs569159850 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11359104 | ATACCAATTATGTTT[A/T]TATATAAACATTGAT | 10533 |
| rs569166945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11554613 | CTGTTGGTTCCACCA[A/G]GTGGTTCACACACTA | 10533 |
| rs569174106 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11387351 | TGTGGTTTTTAAGAC[G/T]ACCTAATTAGTAGTT | 10533 |
| rs569187405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11278471 | GGGTCCGTGACTTCC[C/T]GCAACAGAACTCATT | 10533 |
| rs569197331 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11484439 | AAAAACGACAAACCC[-/A]AAAAGGGTTAAGTCT | 10533 |
| rs569202656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11293683 | CGAAACCTGTCTCTA[C/T]TAAAAAATACAAAAC | 10533 |
| rs569215653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335577 | CTTCCATGGGGTAAT[A/C]ACTTAATTCTGCCAA | 10533 |
| rs569221252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482911 | ACCCAGATTGGGAGA[C/T]AGAACATTTCCAGGA | 10533 |
| rs569222213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11511668 | CTCGTCGGGGAGGCT[C/G]CGGCCGCACAGGAGC | 10533 |
| rs569237768 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11467222 | CAAAGAGATAGCATG[A/G]GGCAGTGGTTAGTAA | 10533 |
| rs569239158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11444295 | TCATGTGCAGCATTT[C/T]TCTGGGTGTTTCTCA | 10533 |
| rs569251805 | in-del | -/CAGGCTATACTGTATTTGT | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11279827 | ATTCTGTACAAACGC[-/CAGGCTATACTGTATTTGT]TTTACCTCCAAATTG | 10533 |
| rs569253049 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11295830 | TCGCTCTTGTTGCCC[A/G]GGCTGGAGTGCAATG | 10533 |
| rs569262413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11455326 | CCAGTAAGACTAGCA[C/T]TTGCCACCCAGAATG | 10533 |
| rs569267709 | snp | G/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11282280 | GCATGTGAAGGTGAA[G/T]GATATTATAGCAGAA | 10533 |
| rs569289267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479520 | TCTCTTGGAGCAGTG[C/T]ATCTTTCAACTAGTC | 10533 |
| rs569290516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423199 | GAGAGAGATGGAGGA[A/G]TGGCCAGTTGGTGAA | 10533 |
| rs569291799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11438021 | AGTTTTTTCCAATAA[C/T]ACTTAAGCACTGGTC | 10533 |
| rs569304747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11390087 | TTGTTGTGTTGAAAC[C/T]TCCTACGTATCCCAA | 10533 |
| rs569320675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11437440 | CCATCCATAGAAGAC[A/G]TCGCAGATAAAGGGG | 10533 |
| rs569337707 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11326216 | TTGTAAGCTGTTTCA[A/G]TGTTTTGGAAGTAGA | 10533 |
| rs569342500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417234 | CGTCCTTTTTAACCT[G/T]CTGTCTGCTGGATCT | 10533 |
| rs569359646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387089 | CTCCTGGGACTGGTG[A/T]TGACATCAGAAATAA | 10533 |
| rs569368571 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11391933 | TGTGGTAGGATTCAT[A/C]TGCATAGAATTCCAT | 10533 |
| rs569378538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11484764 | TGTTGTCATTGTTCA[A/C]TTCCCACCTATGAGT | 10533 |
| rs569391778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364906 | ATTCCATTCTGCGGG[A/G]TAGTGATGGGAGGAA | 10533 |
| rs569422017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11386511 | GGGTTTTAAATCTCA[A/G]TCATTTACAAGGACT | 10533 |
| rs569422845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11517094 | TCTCAAAAAACAAAC[A/G]TATTACTAAGTGAAA | 10533 |
| rs569426578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11409363 | CTCCACTCAACCACA[C/T]GATCGTGAGGGTAAA | 10533 |
| rs569447857 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11422272 | GGTTTCATCTATGTT[-/A]AAAAATCTGTTGTTT | 10533 |
| rs569462540 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11506183 | ATTAGTTAAGGTATA[A/G]GCTAAGGTACTATAA | 10533 |
| rs569464688 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11463749 | TGTGACTACTGGCAG[C/T]TCCAGAGCCTCATAA | 10533 |
| rs569465083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11495688 | AAAACTCCTGAAGCT[A/G]TAAGTCAGTCATGAC | 10533 |
| rs569489824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11537454 | GCGAGAGCCAAACAT[A/G]TCATAGCACATGGGG | 10533 |
| rs569491834 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11419517 | CAAGATCACGTCACT[C/G]TACTCCAGCCTGGGC | 10533 |
| rs569494038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11323757 | TGTTAGTTGGGCTCT[C/T]TCTTCACTTAGTGAT | 10533 |
| rs569505424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288486 | AGCTGCTAGTCTTTT[A/C]TCTCTCTCTTTGTCT | 10533 |
| rs569512408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11502924 | GAAAGTTTGCTTTCT[G/T]TTAAGGGTAAAACAG | 10533 |
| rs569519661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11503962 | AATAATAGAGTTTGC[A/G]GAAAGGAAAACATAG | 10533 |
| rs569519872 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11556071 | CACGTACACTATGTG[A/G]TTTAAGAGCACTTTA | 10533 |
| rs569530932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496080 | GTTTAAGTGACACAG[C/T]GAGAGTGGGTACACA | 10533 |
| rs569535936 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313719 | GTGATCCTCTCATCT[C/T]AGCCTCCTGAGCACC | 10533 |
| rs569536594 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11371801 | TTTGTGCTTCCACCA[A/G]CACTAGTTGTGTTTC | 10533 |
| rs569553848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11371685 | CATTAGGCATTTGAG[A/G]ACCACTGCTTCTGTC | 10533 |
| rs569556459 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479107 | TAATCTTCTCAATGG[C/T]AGGCTCCAGCATTGC | 10533 |
| rs569557516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11282767 | TTTAACAGCCTTGCA[C/G]ATTGTTTCTGAAACT | 10533 |
| rs569562922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11542273 | AGATCGTGTAGATAT[C/T]GGTGCTTATTTAGCG | 10533 |
| rs569599029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11380894 | CTGTGGAAGAAAGAG[A/C]ATTCTAGGGATGTAT | 10533 |
| rs569604519 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11345325 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGT | 10533 |
| rs569610637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11471826 | CTCACTGCAACCTCT[A/G]CCTCAGGTTCAAGCG | 10533 |
| rs569618477 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11363972 | GTCATTTAAGTTTAT[C/T]GCCACTCTCTGACAG | 10533 |
| rs569620099 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11469023 | CTCTCTCATCTCTTC[C/T]TGAGTTTGCTTATTT | 10533 |
| rs569620478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11433061 | CTTTGGGAGGCTAAG[G/T]TGGGAGGATTGCTTG | 10533 |
| rs569622315 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11425690 | AGGATAACATATATC[A/C]AAAAAAAACACATAA | 10533 |
| rs569625755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11393072 | TAAACTTTTCATTGG[C/T]GCAGGTGATGGAATC | 10533 |
| rs569641328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11338794 | AAACTGGGGCCCAAC[C/T]AGCTTTCAAGGATAA | 10533 |
| rs569655889 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11402489 | CTGATAAGACCCTGA[A/G]AAACCAGGGTGTGAA | 10533 |
| rs569658995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296770 | CTTGTTCCTTCTGCC[C/T]TCCACCCATCTTCCC | 10533 |
| rs569672924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353421 | TGCACTCCAGCCTGG[C/T]GACAGAGTGAGACTC | 10533 |
| rs569678207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11297537 | CCCCGGAGAGTATGG[A/T]GGGATTATAGAAAGT | 10533 |
| rs569682579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426253 | AAAGTAGTGTTTCAT[A/T]GTGGTTTCAGTTTTC | 10533 |
| rs569714476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555675 | GAGGGAGGGGTCAGA[C/T]GGCTCTACCATGGGT | 10533 |
| rs569716236 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11501905 | ATGTTGGCCAGGCTG[G/T]TCTAGAACTCCTGAC | 10533 |
| rs569726684 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11300657 | ATAAAGATAGTCTCC[A/C]ACTTATGGTGGTTTA | 10533 |
| rs569729191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11519762 | GAGACGGGGTTTCAC[A/C]GTGTTATCCAGGATA | 10533 |
| rs569736526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11521352 | AGAGTCACAGAGGGT[A/G]ACCTCACCTGGACTC | 10533 |
| rs569736591 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11286629 | AGGGTCTGGCTCGAT[C/T]ACCTGGGCTGGAGTG | 10533 |
| rs569743495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11412990 | TCTTTTTTTAGATTG[C/T]TCATTATTAGTGCAT | 10533 |
| rs569745057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11393656 | GCAGAGAAGAGAGAA[A/G]AGAATGATAATTTTT | 10533 |
| rs569748473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306142 | CCTTTGGGGGCAATG[C/T]AGAGTGTGTAAACCT | 10533 |
| rs569758324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11539761 | CAATCAAATATATGT[A/G]AAAGTGCACATTTCT | 10533 |
| rs569774163 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11305345 | CTTGAGTTCTTGGTA[C/T]GCAGTTTTCTCCTTT | 10533 |
| rs569774565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11391994 | TTAAATTTTTAGCAG[C/T]TTCGAGGACTTAATT | 10533 |
| rs569774832 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ATG7 | GRCh38.p7 | 3:11273201 | ACAAAACCCTGTTCA[A/T]CTGTAACCAGTCATA | 10533 |
| rs569781961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11513170 | ACCAGACTCAGGAGC[C/G]CAGCTGGCTTCACCC | 10533 |
| rs569803242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465985 | TCTTTTCATTTGTGT[C/G]TTTCACAGAGGGCAG | 10533 |
| rs569804947 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11432511 | GGAGAAGCTTGGGAG[G/T]GGGGGTAAAGGATAA | 10533 |
| rs569806332 | in-del | -/TTGATCA | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11388263 | AGATTGTGTAGTCTC[-/TTGATCA]ACTATTTCATTTCTT | 10533 |
| rs569815274 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11341999 | CCTCCCTGCTTACCC[G/T]CCAGTTTAATTTTCT | 10533 |
| rs569823570 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11279746 | AAACCCCACCTTGGC[G/T]TAAGGGTTTCTATAG | 10533 |
| rs569834881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11413301 | ATTTGCTGTGGGTTT[A/T]GTTGCATATGGCTTT | 10533 |
| rs569839583 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11471250 | CCTACCGCTGGCCCC[-/A]GCTTCCTCTCAAGCT | 10533 |
| rs569843964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11496775 | TTCTGAAGCTGGAAA[A/G]GAAAAATAAAGCTGT | 10533 |
| rs569848316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11527800 | CTCAAGTTACAGTTA[A/T]ATAAGGCCTTTCAGA | 10533 |
| rs569862894 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11386858 | GTTCCCAAAAGGAGA[C/T]GGAATATACAGCCAG | 10533 |
| rs569871835 | in-del | -/T | 3.30376e-05 | 0.0040642 | intron-variant | ATG7 | GRCh38.p7 | 3:11331312 | GACATGATACTCGAC[-/T]TACTCAGAAAGTCTT | 10533 |
| rs569874723 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11430858 | AAGAGAACAAATATT[G/T]CACTTAGTTTTAAAG | 10533 |
| rs569882526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11419689 | AAAATTAGAAGGGTG[C/T]GGGGGCGCTGAAATG | 10533 |
| rs569891241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11453091 | CAGCTCTGTCCACCA[C/T]GCCTTTAGAGAGGCA | 10533 |
| rs569914754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11441955 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCCAATT | 10533 |
| rs569920170 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11459211 | AAACATCAGTCATTA[G/T]GGTGAAATGTCAACA | 10533 |
| rs569922373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11334020 | TCCCAAAGTGCTGGG[A/G]TTACAGGCATGAGCC | 10533 |
| rs569927424 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11316723 | TGAATGAAAGAGTAC[C/T]GTAAATGTCTTTTAG | 10533 |
| rs569943324 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11485358 | TGAGAAGTGTCTGTT[A/C]ATATTCTTCGCCCAC | 10533 |
| rs569944184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11509484 | CCTGGTGCAACTCCT[C/T]GTATGTCACAGACAT | 10533 |
| rs569950695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11289178 | AAGCTAAGCAGAGGC[C/G]GAAGTTTCACTTGCA | 10533 |
| rs569958233 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11454652 | TTAGCTTGAGTAAAT[A/G]AAGGTTGAGATTTCT | 10533 |
| rs569976829 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11461871 | CTTTACTAAAAATAC[-/A]AAAAAAAAATTAGCT | 10533 |
| rs569982376 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11313190 | ATAAGCTGGACAGAC[G/T]TTGTTTGCATAGCTT | 10533 |
| rs569986577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11306760 | AGGCTTTTAGGGGGG[A/C]ATGGTGCCTGTTTTT | 10533 |
| rs569991846 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11309209 | ACGCTCATTTGATTA[A/G]TGGCCAGATAGTGCT | 10533 |
| rs569992204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11434640 | AAATGTGTACCTTTT[A/G]TTTGCTGTCAGAGTT | 10533 |
| rs569996950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11545231 | TGGACTTCACTCTCC[C/G]TCTGTGCAAGGGGAA | 10533 |
| rs570014808 | snp | A/G | 0.000943107 | 0.0216948 | intron-variant | ATG7 | GRCh38.p7 | 3:11306917 | TCCCAGCTGTGCCTG[A/G]CTAACCGTGTTTCTC | 10533 |
| rs570014868 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11409975 | TTGCTGACTGTAGCT[A/G]TACAGTTGGTCTAGA | 10533 |
| rs570020996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11353559 | TCCTCACTGTTGGAG[G/T]TGGGGCCTGGTGGGA | 10533 |
| rs570022354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11299258 | AGAAATTGGATGGGG[C/T]GCCTTGGGCTCAACA | 10533 |
| rs570027526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11312434 | CCTCACAAATCCTTT[C/G]CCCTGGATCTCCTAC | 10533 |
| rs570032648 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550788 | TTTTGACTGTTTTCC[C/T]GTGCATATTGCATGC | 10533 |
| rs570037996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11485679 | TATGGTTTTAGGTCT[A/C]ACATTTAAGTCTTTA | 10533 |
| rs570048394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11534475 | CCTGTGGGTTAGACA[C/T]GCTCATGGAGGAGAG | 10533 |
| rs570056036 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11382021 | TATACAGAGTCATGT[C/G]ATAGTTGTTGTTTCA | 10533 |
| rs570071991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11480374 | AGACCCTGTCTCTAC[A/G]AAAACATTTAAGATT | 10533 |
| rs570087180 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379462 | TTACATTTTATCTCT[A/C]TCTGTTCCAAATCAA | 10533 |
| rs570089439 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11319325 | TCAAAAATAGGCATT[A/C]TTTTCAGTATGAAAT | 10533 |
| rs570113971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11369050 | CTGGGAAAACTCTAA[C/T]TGAGTCACATGCTGA | 10533 |
| rs570132059 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11523502 | AGAGGTGATATGCAC[G/T]GAAGTGTTTGATTTA | 10533 |
| rs570137349 | snp | A/G | 0.000138648 | 0.00832495 | intron-variant, synonymous-codon | ATG7 | GRCh38.p7 | 3:11510256 | CTGCACTCAGGAGTC[A/G]GCTGCCTGTCCTGAA | 10533 |
| rs570146892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11316400 | TTTGTATCTTTGTTT[C/T]TCCTCGTGTTGTATC | 10533 |
| rs570163804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11453511 | GGTGGAGAAGTAGGC[G/T]GGAGGAAGCTATTTA | 10533 |
| rs570171350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11421068 | CCACAAAATACTTTT[C/T]TTTTGCTAAAAAATG | 10533 |
| rs570171581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11315244 | GTGATCAGTCATTTC[G/T]AGTCTTCTGGTTTTA | 10533 |
| rs570173903 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11361578 | GTGAGCCACCACGCT[C/T]AGCCAATAATGAATA | 10533 |
| rs570175759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11409221 | ACAATTTTTCAATTT[A/G]CCATGGTGTGAGAGT | 10533 |
| rs570186801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290947 | CTCAGCCTCCAAAGT[G/T]CTGGGATTACAGGCG | 10533 |
| rs570191829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11467274 | CTGAGTTTAAATTCA[C/G]TACTTATTAGCTGGG | 10533 |
| rs570201474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340290 | CCTCAGTGGGGTTAT[A/G]CCTACCCCAGAAAAG | 10533 |
| rs570201732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389301 | TATTCCTGAAGTTAC[C/T]CTTATGACTTGTTCA | 10533 |
| rs570220913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11278441 | TGCTGCAGCTCCAGC[C/T]GGTCCCTCCGTTCAG | 10533 |
| rs570236737 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | VGLL4, ATG7 | GRCh38.p7 | 3:11557576 | TTGTGAGTAAAGTGA[A/G]TATCAAATACCAATC | 10533 |
| rs570238228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552886 | TAGCTAAAAACCCAG[C/T]AAAATGGATGATAAA | 10533 |
| rs570243223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11481335 | TGTTAGATATATTTT[A/C]CGATGATAAAAAAAT | 10533 |
| rs570249010 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11312552 | CTCTAATCATGCACT[C/T]GCTTTATCTCTGCTC | 10533 |
| rs570257317 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11345363 | GCAGTGAGCGGAGAT[A/G]GCGCCACTGCACTCC | 10533 |
| rs570291384 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11317006 | AAGCCCACCTCCCCT[A/T]TTTTGTTGTATTTTT | 10533 |
| rs570302965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11395253 | ATAAAAAAGGTAGAA[C/G]ATAGAGTGAGAAAGT | 10533 |
| rs570305032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11442340 | TTCATCTGTAAAATG[A/G]GATAATGCCTACTCC | 10533 |
| rs570309879 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532636 | GCTGAGGCAGGAACA[A/C]TGCTTGAGTCCCCAA | 10533 |
| rs570310404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11329067 | GCCGCTGCACTCCAG[C/T]CTGGGTAATAACGGT | 10533 |
| rs570316370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482440 | GATGCTTATTACTAC[C/T]GTATCTTTTTGGTGG | 10533 |
| rs570318327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11451205 | AAAATAGAAGTAAAG[A/G]TTGACACTTTTTTTT | 10533 |
| rs570323898 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11336588 | AACTGAAAATATAAG[A/T]ATGGTTGTACTTTTC | 10533 |
| rs570339138 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11388723 | GTGAGCCACTGCGCC[A/C]GGCCCCTTCTTTCTT | 10533 |
| rs570345514 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11493373 | TATAGACACAGGATG[C/G/T]GGGGACAGGGCTGGC | 10533 |
| rs570353692 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11456721 | CAATTACTGTTTGGA[C/G]TCAAAAATGTGACGG | 10533 |
| rs570357691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11488654 | CGGCGCCGTGACCTC[C/T]TCTCAAGATGTGAAT | 10533 |
| rs570358566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11347439 | AATAATTTGTGAGTC[A/C]TTTTTTGGAGGAGTT | 10533 |
| rs570385557 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11372031 | TGCTTTTTGCATGCT[A/G]TCTGCCGTGTTTTCA | 10533 |
| rs570389583 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11455093 | TTAACAACAATTACT[A/G]TACAGATAGAGTCAC | 10533 |
| rs570389731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11438172 | GCTCCAGCAGGCCTC[C/T]TCTAGGTGAGCGTCT | 10533 |
| rs570391599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11444454 | TCTAAGATTTCTTTT[G/T]CCTGCCAAAGACCAA | 10533 |
| rs570403519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11403050 | GCTGTAGTGATTACA[A/G]CGTTGAATAGTACAC | 10533 |
| rs570412903 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323131 | TTAAGGTTCATAATC[A/C/G]GTGGTGTGCTGGTAA | 10533 |
| rs570421013 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271993 | GGTTGGTCACTGTCG[A/G]CGTTCACTGGCCTTT | 10533 |
| rs570433028 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11371558 | TAAATCAGAAGACAG[A/C]CTAATCCAGGGATTC | 10533 |
| rs570451840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11438772 | ATGTGAGAGAGAAAG[C/T]GAAAACTAAAGGAAT | 10533 |
| rs570454569 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11488490 | TCTGCAGCTGGGGCC[C/T]GCGGGTGTCAGCGCC | 10533 |
| rs570503361 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11479588 | ATTTCAAGTTGGAAG[A/C]CCAAAGTAAGGCATG | 10533 |
| rs570523259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11536806 | TAGGCCACACCCCTC[C/T]CTGAGCCTCCATCTT | 10533 |
| rs570528191 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11313869 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 10533 |
| rs570529361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ATG7 | GRCh38.p7 | 3:11450768 | GAACAGTCTTCTAGA[A/G]TGATATAGGTTCTAG | 10533 |
| rs570533655 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11271463 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 10533 |
| rs570547384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11457936 | TATGGAGGAAGTAAC[C/T]GGTAAGTATATATTG | 10533 |
| rs570558100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11492942 | CTTAGCTCCGCCGTC[C/T]ATGGACAGCAGCGTG | 10533 |
| rs570579674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11364838 | TTCATATCCACCCTA[C/T]TTACCCTGCAGCTGG | 10533 |
| rs570582042 | snp | A/G | 0.000744595 | 0.0192806 | missense, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554822 | GCAGATCTGGGACAT[A/G]AGCGATGATGAGACC | 10533 |
| rs570592757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549434 | GTAGTCCTGTGCTGT[A/G]TATCAGACCTCCAGA | 10533 |
| rs570598186 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11554977 | GTCTGGGATTCCCCC[C/T]TCTGCTGCCCAGGAG | 10533 |
| rs570598561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11295088 | CTGCACTCCAGCCTC[A/G]GCAACAGAGCAAGAC | 10533 |
| rs570608194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11511851 | CAGGTGCTAAGTCCC[C/T]CACTGCCTGGGGCCA | 10533 |
| rs570628693 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11397821 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCGGCA | 10533 |
| rs570636577 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG7 | GRCh38.p7 | 3:11343952 | TTCTGGGAGCATGGT[A/G]TATCTCTTAATTAGA | 10533 |
| rs570638713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11423963 | TTTAAATGTGCCAGT[C/T]AACCTCTCTTCTCCG | 10533 |
| rs570645688 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11477536 | TTGCCGCAAAAGATA[A/C]GGGCGTTTGTTAGAC | 10533 |
| rs570659741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11337140 | CCCACTATGGGAGAC[A/G]GCACCTAATTTTTTC | 10533 |
| rs570662756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11303209 | AGGGACATTTATCAC[A/T]CCACTCAGATTCTAC | 10533 |
| rs570686368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11384781 | GCCTGGGTAACATGG[C/T]GAAATCCTGCCTCTA | 10533 |
| rs570692381 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287122 | CCACTCACAAGGGAT[G/T]AGGGACATTGAAAGG | 10533 |
| rs570716017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11349933 | AAAATCTTGACAGTT[G/T]TCTTTTTTTAAGGTC | 10533 |
| rs570726432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11483270 | TCACAGAAGCTTGAC[A/G]AGAAGAGAAACAGAC | 10533 |
| rs570731664 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11293862 | TATCGAGAGAAAAAA[A/C/G]AAAACATTAGCCGGG | 10533 |
| rs570747441 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11371821 | GTTGTGTTTCTAAAA[-/G]GACCCTTGGCACCTT | 10533 |
| rs570755875 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11309047 | CTCAACAAGTTCCTC[C/G]TCTTGACATTTGCAG | 10533 |
| rs570777066 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11539574 | AGTGGGCCTGCTGGC[C/G]GGGGGTCGCCCACTT | 10533 |
| rs570785928 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11405446 | TTTTTCTTGAATACA[C/T]AGCCCCAGATTTTGT | 10533 |
| rs570788822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11366417 | TTTTTTGACATGCAT[A/G]TGTTAATCTTTTCTA | 10533 |
| rs570799016 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ATG7 | GRCh38.p7 | 3:11451864 | ATATATATATACGCC[C/T]TTACATACACACACA | 10533 |
| rs570805795 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11353124 | TGGAAAAGAAAAAAA[-/T]AATGGGTGATAGCCC | 10533 |
| rs570810648 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11511181 | GAAGGGGACCTGAGC[A/G]GGTTGCCAATGCTGG | 10533 |
| rs570812110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11323924 | TTTGTTAGATTAGCA[G/T]GTTTTATGGGATCAT | 10533 |
| rs570812939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382524 | GTCACTTTCATTCCA[A/G]TTTCTACTTATTGTC | 10533 |
| rs570817020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11470735 | GCCACCAGAGGACAT[A/G]GAGTAGAGGCCTTCC | 10533 |
| rs570827252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11512050 | GGGGCTCCCACAGTG[C/T]AGTGGGGGGCTGAAG | 10533 |
| rs570827957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11358837 | AATCTTTTGAGATAC[C/T]CTACACTGAAAGATA | 10533 |
| rs570831387 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11449637 | GCATCAGATGAACGC[C/T]TGGCATAAATCTAAC | 10533 |
| rs570832276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11538062 | GATGACCCCTGTTGT[A/C]CAGCTGGCTAGGAGA | 10533 |
| rs570842542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11494165 | CAGGCAAGATGGGAG[A/T]TCAGTCTCAAATCCA | 10533 |
| rs570855479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11500699 | GTTACCCAGGCCGGA[C/T]GTCTCACTGCAACCT | 10533 |
| rs570861165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11411213 | TGTTGAGCATCTTTT[C/T]GTGTGCTTATTGGCC | 10533 |
| rs570878615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464754 | TACCTTTTATTGCCG[A/C]ATAGGTTCTGGAGTC | 10533 |
| rs570895985 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11485448 | GGACATTAGCCCTTC[A/G]TCAGATGAGTAGGTT | 10533 |
| rs570903800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11280031 | AACTAATGGAAGCCC[C/T]AATTTCATTTCTTTT | 10533 |
| rs570919558 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11462643 | TGGGCCAGATAGAGG[A/C]GGTGTGGCTCTGAAT | 10533 |
| rs570920853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11546451 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 10533 |
| rs570927982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372147 | CAGGGATTTCCACTC[A/G]AAGTGCTTGGCCCTT | 10533 |
| rs570945543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11460617 | TGTAGCAATTCACAG[A/G]ATTCATTCCATAAAA | 10533 |
| rs570958179 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11438281 | CCATCCTCCATCCAG[G/T]GTCCCCAATGGTGGA | 10533 |
| rs570971842 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11466735 | TCATCTATAGAAACT[C/G]AACTGTTGGATGCAT | 10533 |
| rs570973251 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11516163 | ATCCCCAACTCATCA[-/G]GGGAAGATATACAGA | 10533 |
| rs570977441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286966 | GAAATGGTGTTCTGC[C/T]ATGTTGCCCAGGCTG | 10533 |
| rs570979227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11351640 | GTGTTACTCTGTTTT[C/T]CCTGTTGGACTATTA | 10533 |
| rs570988343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11552244 | TTTTTCCTTAGGGTT[C/G]AATGTTTTTAAAGGT | 10533 |
| rs570992966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11399101 | GCCTGTAATCCCAGC[A/C]CTTGGGGAGGCTGAG | 10533 |
| rs571008087 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11431560 | CACTCCCTGTTCCCT[C/T]CTCCTTCCAGCCCCT | 10533 |
| rs571022264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11398567 | GATATGGAGAAAGCA[A/G]TACTTAATAAAAATG | 10533 |
| rs571024307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464756 | CCTTTTATTGCCGAA[C/T]AGGTTCTGGAGTCTG | 10533 |
| rs571025787 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11423016 | CACCTTGGCCTCTCA[A/G]AGTGCTGGGATTACA | 10533 |
| rs571034769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11405216 | GGATCTTCCTGACAC[C/T]ATACAGGTGACATTT | 10533 |
| rs571051185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11310384 | AAGTTTTCCTTCCCC[A/G]ACCTCCCACCGTTCC | 10533 |
| rs571056503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11333308 | CCAGGAAATTTTCTC[C/T]AGGCAGTTTTTTCAG | 10533 |
| rs571058521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11340231 | AGGAACCTCAGTGAA[A/G]GGGTGCTGCAGTTAC | 10533 |
| rs571067090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11273171 | GCGTTTAAAAACATT[A/G]GCAACTCAGTTTTTA | 10533 |
| rs571087160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11310962 | GGGATAAATTGTAAG[C/T]ATTGCTAGTTAAAGA | 10533 |
| rs571118241 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11550433 | GAGACAGGGTCTCAC[G/T]CTCTGTTGCCCAGGC | 10533 |
| rs571121459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11532204 | AGTATGATTTCTGAT[G/T]TGTTGAGCATTTATT | 10533 |
| rs571123923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11445846 | TTTTTGCCAATCTGT[A/G]TAACAGTATCATATT | 10533 |
| rs571131689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11274173 | TCAACCACAGGTTCC[A/G]TTTTTCGTTCCCAGC | 10533 |
| rs571136861 | in-del | -/AA | 0.0479149 | 0.147179 | intron-variant | ATG7 | GRCh38.p7 | 3:11433290 | CCCTGTCTCTTATTT[-/AA]AAAAAAAAAAAAAAA | 10533 |
| rs571140578 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327087 | GCAGAGGGGGAGTCC[A/G/T]TGTATTGAAGCCTGG | 10533 |
| rs571146150 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11416952 | TGAGATTTTTTATTC[A/C]TGTGTTATTGTTCAA | 10533 |
| rs571146415 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11488841 | TGCATCAATGTTCAT[C/T]AAGGATATTGGTCTA | 10533 |
| rs571151552 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG7 | GRCh38.p7 | 3:11489404 | GCTAGTGGTCTATCA[A/G]TTTTATTGATCCTTT | 10533 |
| rs571164382 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11540491 | AAAAAATAAAAATAA[A/T]TTCACTGGGCATGGT | 10533 |
| rs571171707 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304061 | GCACGACTGCACTCC[A/G]GCCTGGGTGACAGAG | 10533 |
| rs571199063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11275825 | ACTCCATCTCAGACC[A/G]GCTTCAGAATGATCA | 10533 |
| rs571202926 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11495857 | TCCCTTTATTTTCTC[C/T]TAATGGAATGGCCAA | 10533 |
| rs571204372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11461238 | TGCACTGGCATTTTA[C/G]CCAAGGCCATTCTGT | 10533 |
| rs571217361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11381600 | GCATTTTTCTTTCAC[A/G]CTTATTGTAAGCTTT | 10533 |
| rs571224598 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11362179 | GAGTCAAAAATATCT[C/T]TAACAACCTCTTAAT | 10533 |
| rs571229024 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11512344 | TCCACCTCTGGGTCA[A/G]GGGCTCCAGAGCCTG | 10533 |
| rs571244240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11327823 | ATGGGTGTATGAATC[A/G]CCTGGGTTCTTATTA | 10533 |
| rs571264418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11414174 | AGGTTCAAGTGATTT[C/T]CCTGCTTCAGCTTCC | 10533 |
| rs571281815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420576 | GCTATTTACAGGCAT[A/G]TCTTAGATTATGGGG | 10533 |
| rs571283118 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11474239 | TCTGTTTTCATGGAG[C/T]CTACTTTTCTAGTTC | 10533 |
| rs571290399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11482105 | CTCTCCTGATGCCCC[A/G]GTTCCTTCTCTCATC | 10533 |
| rs571294794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11504114 | CTAAGGTTCATCATA[A/G]TGAATTTCAAAACAG | 10533 |
| rs571296187 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11389477 | AGAATAAGCTACATG[G/T]TTCTCTTCTCTAGAA | 10533 |
| rs571320261 | in-del | -/ATATATATATATA | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11497390 | TATATATATATATAT[-/ATATATATATATA]ATTTAGCCAGGCATG | 10533 |
| rs571320871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11382148 | CACCAGGATCAAGGC[C/T]ATGCTTGTGTCTTGA | 10533 |
| rs571321414 | in-del | -/TTTG | 0.157163 | 0.232123 | intron-variant | ATG7 | GRCh38.p7 | 3:11385020 | TAAATAGTGTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 10533 |
| rs571329587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11388705 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACTGCG | 10533 |
| rs571333035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11389964 | GGATTTCTCTTAGTT[C/T]TCAGTTGTACTTTGC | 10533 |
| rs571335234 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11383003 | CTGATCCTTTAAAAC[G/T]GAATGCTTCAATGTG | 10533 |
| rs571336449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11393761 | TCTTGGCTCACTGCA[A/G]CCTCCACCTCCAAGG | 10533 |
| rs571337825 | snp | A/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11464615 | TGCCAGATGGACTTG[A/T]TGTTTTAATTATACC | 10533 |
| rs571347169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11428187 | TCAAATGATTGCATG[C/G]GTGCAAAGATCTATA | 10533 |
| rs571349839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11283144 | CCTTTAGAACTTGTT[C/G]TTTTGGACTTCTCGA | 10533 |
| rs571353984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11401133 | AAAACTCTCAGACCC[C/T]GCCCCAGACCTAATT | 10533 |
| rs571356345 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11476042 | GGGTCTTTTCATAGC[A/C]GCAAGGCATCATCAC | 10533 |
| rs571357472 | in-del | -/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11365512 | CTTATTTGGAAATCA[-/T]TTTTTTTTTAGATTC | 10533 |
| rs571372983 | snp | A/G | 0.000808625 | 0.0200913 | intron-variant, missense | ATG7 | GRCh38.p7 | 3:11510186 | TTACCCCCTTTCAGG[A/G]TCATCTTTCTTTCAT | 10533 |
| rs571380019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486721 | TGTCCCATCAGTACC[G/T]AATTTATTGAGAGTT | 10533 |
| rs571385551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11290075 | GGGTAGGAAATAGAT[G/T]CCTGATTCACAGGGT | 10533 |
| rs571386840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11449507 | AGAGGGTGAGAGAGA[G/T]TATGATTGGTTTTAG | 10533 |
| rs571389892 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11270484 | GAACTAGCATACTGT[C/T]TCATGTGTCCGTGTG | 10533 |
| rs571395861 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11442059 | CACCTGCTTCGACTT[-/A]CACAAAGTTCTGAGA | 10533 |
| rs571409235 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11273187 | CAACTCAGTTTTTAC[-/A]AAAACCCTGTTCAAC | 10533 |
| rs571421640 | snp | A/C | | | intron-variant | ATG7 | GRCh38.p7 | 3:11536519 | CTGGGGAAGAAGCCA[A/C]AACTTCTGTTTCCCA | 10533 |
| rs571469586 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11532809 | GGATGGGTCTAGATA[C/T]TGCATGAGATGTCGT | 10533 |
| rs571486268 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11388520 | TGCAAGCTCCGCCTC[C/G]CAGGTTCATGCCATT | 10533 |
| rs571502035 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11505369 | GGATATAGTCACACT[G/T]AAGTATATGGGCTTT | 10533 |
| rs571516372 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11440907 | TAGGCTGGTCTCAAA[C/T]TCCTGACCTCAGGTG | 10533 |
| rs571523282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515868 | GAGAAGTTGAAAAAA[G/T]CAGTGCTGTGGGGCT | 10533 |
| rs571527389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455166 | TGAGGAACTGGAATT[A/T]ACTGGGCCTAGAAAC | 10533 |
| rs571535837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11482068 | TGGGAGCTCATGAGC[A/G]GTCCTAAGAATCCTC | 10533 |
| rs571590751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11285502 | TATTCATGGATAACA[C/T]ACATAAAGTGCACTG | 10533 |
| rs571595691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11301063 | AGGTGAAAGATGATA[C/T]AGAACTAGCGAAGGA | 10533 |
| rs571598548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11516418 | TAAACACCTACTAGA[A/G]TGGCCAAAATGCAAA | 10533 |
| rs571600039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11372033 | CTTTTTGCATGCTGT[C/T]TGCCGTGTTTTCATT | 10533 |
| rs571604276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11535653 | GAGGCACACAGGGTC[C/T]CTCTGAGGAGGGCTC | 10533 |
| rs571613808 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11519356 | AGACTGTGTTTCCTT[A/G]ACGCAGTATTTCTGG | 10533 |
| rs571616689 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11429766 | CAGCCTGGGCAACAC[A/G]GCGAAACCTCATCTC | 10533 |
| rs571624890 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11437302 | CTTAGTCTCTGTGCA[C/G]CTCCTTTAGCCTTTT | 10533 |
| rs571626533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11284625 | GGTGCAGTCATGGCT[C/T]ACTGCAGCTTGGATT | 10533 |
| rs571628172 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11399878 | TGCCTGGCGTGGAAG[C/T]GACTTTGTAGGGACT | 10533 |
| rs571630803 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11530346 | TGCCTGGCCGTACTC[C/T]GAGAAGCACTCTGCA | 10533 |
| rs571632389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11429765 | CCAGCCTGGGCAACA[C/T]GGCGAAACCTCATCT | 10533 |
| rs571644229 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11320892 | TAATGTGAGCATTCT[A/G]TTGTCTGGTTAAGGC | 10533 |
| rs571667214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11287268 | GATTAAATATAGCTG[A/C]CAGGGGAGGAGTATG | 10533 |
| rs571678349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341390 | TGAAGGATATTAGAA[G/T]AATTATTTCATGGAA | 10533 |
| rs571683423 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11470891 | GTATTACTCTCGTTC[A/C]GTCTTTCTCCTTTGA | 10533 |
| rs571690102 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11512187 | CCAGTGACCTTGAGT[A/C]TCCTTAACTTTCCAA | 10533 |
| rs571693173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11515881 | AAGCAGTGCTGTGGG[A/G]CTTGAAGCCAGCATG | 10533 |
| rs571723085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11417624 | TTCCATTATAATAAT[C/G]TGCCTTTTAATTGGT | 10533 |
| rs571730962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11529737 | GTGGCAAGCATGGCA[A/G]GGGACACCCCACACG | 10533 |
| rs571736796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11307437 | TGGAGAGGCTTGGCA[A/G]TCCTGTGCACCATGG | 10533 |
| rs571800613 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11288172 | AGTATTACGTGGCAA[A/G]TAATCATCCAATATA | 10533 |
| rs571804740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11286549 | GTTTTTGTTTTGTGT[G/T]TTTTTTTTTGTCTTT | 10533 |
| rs571810587 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11443869 | TTAAAACATTTTATA[G/T]AGAGAACAAGTATGA | 10533 |
| rs571812646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11436603 | GCACACAAAAAATGT[A/G]CACAGTGTTCCTAAC | 10533 |
| rs571819634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11542191 | GGAGCTGAGAGCCCC[A/C]AAACCAGTCTGCTTC | 10533 |
| rs571846481 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11327312 | TTCTACAGTCAGGAA[-/T]TTTCTTACAATTGTG | 10533 |
| rs571854698 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11304505 | TTCTGGGTTCCCAGC[A/G]TTCCCTGTGGGCATG | 10533 |
| rs571855016 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ATG7 | GRCh38.p7 | 3:11511897 | TGCTCCGAATGCGGG[G/T]CCCACCAAGCCCACA | 10533 |
| rs571860160 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11374124 | CCTCAAATTCATATG[A/G]AAGTGCAAGGGACCC | 10533 |
| rs571870212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11468412 | CCTCCTCCCCACTCC[A/G]TGTCCCCAGTCCATC | 10533 |
| rs571891180 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11378841 | CTTTTTCTTTAAATA[A/G]TTTGTCAAATTGTTT | 10533 |
| rs571899357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11424097 | AGCTCCCCTGCCTCC[C/T]GTCGCCTGGTCCTTT | 10533 |
| rs571905832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11455990 | CTTTATTTAGATGTA[A/G]TTCATATGCCCTACA | 10533 |
| rs571911049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11377168 | CACCTGTGGAAGTAC[A/C]CCCTTAGGAGTCTCT | 10533 |
| rs571948855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11554047 | GCCTTGGGCTCTCTC[C/T]CTGGGGGCTGACACC | 10533 |
| rs571953067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11547433 | CTCGTTTCCTATTAT[G/T]AATTCCACGTTTAAC | 10533 |
| rs571962067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549157 | GTTGTGACAAATTAT[C/T]TACTTCCTGTCACCA | 10533 |
| rs571969004 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11344703 | AAACTCCATCTCTAC[-/A]AAAAAAAATATAAAA | 10533 |
| rs571981967 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11411284 | CCCATTTTTAAACTT[G/T]GTTGTTTGTTGTTGA | 10533 |
| rs572005169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11518082 | GTGAGTGGGAGAGAG[A/G]AAGGGGACCAAGGTG | 10533 |
| rs572018287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11335479 | GGCCATGGGTTGGAC[A/G]AGCGTGGTCTTAGGG | 10533 |
| rs572024660 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, intron-variant | ATG7 | GRCh38.p7 | 3:11555102 | GGTCCTCCATGCAGT[G/T]TTTATTTCTTGTCAC | 10533 |
| rs572030540 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11470731 | AGGGGCCACCAGAGG[A/G]CATGGAGTAGAGGCC | 10533 |
| rs572044998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11336749 | AAAATCATAGCTCAC[C/T]GCAGCCTTGACCTCC | 10533 |
| rs572050865 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11296470 | TTCACTTTTACTCCT[C/G]TGCTCTAATCCAGGT | 10533 |
| rs572052373 | snp | C/G/T | | | intron-variant, downstream-variant-500B | ATG7 | GRCh38.p7 | 3:11447441 | CATTGCACTCCAGCC[C/G/T]GGGCAACAGTGCAAG | 10533 |
| rs572056490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11384481 | TCAAAGTGACTTGCT[A/G]TTAGCTTTCTGTGTG | 10533 |
| rs572057230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11470228 | TCACACATCACTTAA[C/T]GATGGGGATGCATTG | 10533 |
| rs572068147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344407 | AATTTAAAGAAGCTG[A/G]TTTCTGTTTCTGCAC | 10533 |
| rs572074502 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG7 | GRCh38.p7 | 3:11309372 | TAAATACCATCCTAA[A/G]TACCATCTAAATAAA | 10533 |
| rs572075972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11440620 | TGAGCCACCGCGCCC[A/G]GCCTTTACTCTTAAT | 10533 |
| rs572085628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11430773 | AATGTTTTAGTCATT[C/T]GTATATTAAGTGCTG | 10533 |
| rs572086867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11431267 | TTAGCTGGGTGTGGT[A/G]GCATGTGCCTGTAAT | 10533 |
| rs572111160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11549679 | AGTTTGTACCTATTC[C/T]GAGTAAGACTGCTGC | 10533 |
| rs572113306 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11403564 | TTTTTAAGGTTTTTT[C/T]TTCTGGTGAGTTACT | 10533 |
| rs572118471 | in-del | -/TGAG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11473664 | AGATAGAGTCACTTC[-/TGAG]TGAGTGCTGTGTGAT | 10533 |
| rs572138434 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG7 | GRCh38.p7 | 3:11502445 | TGATCTCATTGTTCA[A/G]TTCCCACCTATGAGT | 10533 |
| rs572138485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | VGLL4, ATG7 | GRCh38.p7 | 3:11555875 | AAGTGAAAATTGAGT[C/T]GAGCTGACCCTTACA | 10533 |
| rs572188041 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11496577 | TCAAAGAGATTACAA[C/T]AGCCAAGGGCCATTT | 10533 |
| rs572189594 | in-del | -/AC | 0.00557542 | 0.0525036 | intron-variant | ATG7 | GRCh38.p7 | 3:11319289 | CACGACATTTCCTTG[-/AC]AAGGTTTTCACCCTC | 10533 |
| rs572207857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11533024 | TGGCGAGGAGAAGCA[A/G]GCCCCAGCCTGAGCG | 10533 |
| rs572208594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11336282 | CGGGCAATCTGCCTG[C/T]CTCAGCCTCCCAAGG | 10533 |
| rs572231965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11543523 | CTGGTGCCCAGGCTC[A/G]AGGAGGCAGTGAGTG | 10533 |
| rs572253190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11273558 | TTGCTCATAGTAAAC[C/T]TAACAGTGACAGCAA | 10533 |
| rs572256730 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11500834 | CGGGGTTTCACCATG[G/T]TGGCCAAGATGTTCT | 10533 |
| rs572258671 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11436267 | ACAAATTGAAACTAC[-/TG]TGAGATGGCATTCAT | 10533 |
| rs572259776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11551380 | TGAGACTTTGTTAAT[A/G]TATTCACTTTGAGAA | 10533 |
| rs572271091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11279692 | TCTGTCTCAAGACTC[C/G]GTCTCAAAAAACAAA | 10533 |
| rs572273531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11500436 | CAATAACATATCTGA[C/T]CACTATGCAATACAA | 10533 |
| rs572276896 | snp | C/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11494616 | TCCATTTGGCAAAGT[C/G]CTTTTTCATCACTTT | 10533 |
| rs572280077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338983 | GATAGAAATTCAAAA[A/G]TAGGAGAATGGACAA | 10533 |
| rs572287603 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11421075 | ATACTTTTTTTTTGC[C/T]AAAAAATGCTAACAA | 10533 |
| rs572289965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11280213 | CACCATGCCCGGCCC[G/T]TTTTTTGTATTTTTA | 10533 |
| rs572290352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11465671 | TTGGAGAACTGAGGG[G/T]GAAGGATTGCTTGAA | 10533 |
| rs572290689 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11489880 | TTTACATTTGCTGAG[C/G]AGTGCTTTACTTCCA | 10533 |
| rs572327187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11464903 | TTTGGGTACTGTTAG[A/G]ATTAAGTAATATAAT | 10533 |
| rs572333381 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG7 | GRCh38.p7 | 3:11553145 | ATCACCTCCCACCTC[A/G]GCCCCTTCCTCCAGG | 10533 |
| rs572338420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11372332 | TTCTAGACGTTTCTA[G/T]GGAACACTAATGTTG | 10533 |
| rs572341895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11304329 | TGAATTACAAGCGGT[A/C]TAAGCGCATGGCTGT | 10533 |
| rs572349850 | in-del | -/C | 0.204189 | 0.245767 | intron-variant | ATG7 | GRCh38.p7 | 3:11506585 | AAAAAAAAAAAAAAA[-/C]CCAAAAATTAGCTGG | 10533 |
| rs572353291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11466179 | GAAGCTGCTGCAGAC[A/G]TCACAAGACTTGTTA | 10533 |
| rs572368728 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11519851 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCGAGAGG | 10533 |
| rs572371044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11372822 | TGTGTGTGTGCGCGC[A/G]TGTGCGTGTGTGTGC | 10533 |
| rs572375250 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11365979 | AATTCCAGCACTTTG[A/G]GAGGCCGAGGCGGGT | 10533 |
| rs572380029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11296379 | TTTATTCTCTCTTTT[C/T]ATTGCTTGAGTCCAC | 10533 |
| rs572404135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11344911 | TTTACATCTCACTTC[A/G]TAAGTCAAATTGGTT | 10533 |
| rs572424915 | in-del | -/ATTATT | | | intron-variant | ATG7 | GRCh38.p7 | 3:11478144 | AGTCTTGTTAGAGAC[-/ATTATT]AGTATGACCCCATCG | 10533 |
| rs572425313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11358933 | GGTCAATGACAACTT[C/G]AAGGGGCAACAATGT | 10533 |
| rs572434104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11304809 | TGGCCTTAGTATGTG[A/G]AGAAAATTTCTAATT | 10533 |
| rs572439173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11338334 | TGGTGTGTGTGTACC[A/C]CATTTTCTTTATCCA | 10533 |
| rs572456428 | snp | C/T | 8.27493e-05 | 0.00643178 | synonymous-codon, intron-variant, nc-transcript-variant | ATG7 | GRCh38.p7 | 3:11347885 | CACACAGGGTTGGGG[C/T]GTGAGACACATCACA | 10533 |
| rs572463045 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG7 | GRCh38.p7 | 3:11351914 | CATGCAGGTTTGTTA[C/T]ATATGTATACATGTG | 10533 |
| rs572469786 | snp | G/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11551831 | TCAGCTCACTACAAC[G/T]TCTACCTCCTGAGTT | 10533 |
| rs572498705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11314396 | GTTCAGGGAGCAGCC[A/G]TTATTGATTAAATTT | 10533 |
| rs572501933 | snp | G/T | 0.030278 | 0.119257 | intron-variant | ATG7 | GRCh38.p7 | 3:11525585 | TTTTAAACGGAGTCT[G/T]GCTCTGTCGCCCAGG | 10533 |
| rs572521883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332056 | TGAAATACCTACATA[A/G]ATAGAAGCAAAACAC | 10533 |
| rs572531763 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11513553 | TGCGGGGCCTGCCAA[A/G]CCCACGCCCACCCGG | 10533 |
| rs572537778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11443360 | TATAAATGAAAGCAC[C/G]ATGCATGTTTGAGGT | 10533 |
| rs572542007 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11397025 | TGATTTAAAGGAAGA[A/G]AAAAACAAGTACAAG | 10533 |
| rs572542893 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11379915 | AACCAGACGTGCATT[C/T]CATAGATGTGGTCGT | 10533 |
| rs572552737 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11504263 | TTTCAAACAATAAAG[A/C/G]GAAATTATATCTAAT | 10533 |
| rs572555467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11426502 | GTTCTTTTCTAACCA[C/T]TGAACTTTAGAGCCA | 10533 |
| rs572557545 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11452959 | TTCCGTGGGCTGTAG[C/T]GAGCACAGTAGCAGT | 10533 |
| rs572581201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11373748 | TTGCATAAGGTACTT[C/G]GATTTTAGATTGCTC | 10533 |
| rs572585883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11472740 | CCCAGGACTTTTGAA[A/G]ATGGTTCAACTGCTG | 10533 |
| rs572596530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11544750 | GGTCACACCAAAAAT[C/T]CCCCTTTCTTTTCTG | 10533 |
| rs572597928 | in-del | -/AGT | 0.497182 | 0.037434 | intron-variant | ATG7 | GRCh38.p7 | 3:11465087 | TCTCTAAAAACCTAA[-/AGT]AGTGTGTGTGTGTGT | 10533 |
| rs572608142 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG7 | GRCh38.p7 | 3:11513277 | GGTGGTGGATGAGAC[A/T]GGGCGCCGTGGAGCA | 10533 |
| rs572610534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11332776 | TTCATTTTTCAGCCT[C/G]TAAACACTTGGACAG | 10533 |
| rs572623506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11419165 | TGCTAAACAAGAAGT[G/T]AATAAAAACTTCATG | 10533 |
| rs572632027 | snp | C/T | | | intron-variant | ATG7 | GRCh38.p7 | 3:11385462 | CTGTTAGCAGACATT[C/T]ATTTAATTCAACTGA | 10533 |
| rs572654736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11553650 | CGGCCCATCCACAGC[C/T]TGGCTGGGCTGGCAT | 10533 |
| rs572657998 | in-del | -/TTG | | | intron-variant | ATG7 | GRCh38.p7 | 3:11390657 | GTAACTTTTTGACCT[-/TTG]TGGGTGGGTTTGATT | 10533 |
| rs572665153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11387319 | AGAGAACACGGCCTT[A/G]CTTGTTACTTTTGAC | 10533 |
| rs572666537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11297167 | TCGAGACCAGCCTGG[A/G]TGACATGACAAGACC | 10533 |
| rs572670342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11479830 | GTATCTCTCCTTCTC[C/T]ACTTAGGGCTGTGTA | 10533 |
| rs572691670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG7 | GRCh38.p7 | 3:11425909 | TAATTGTACAGTACA[C/T]ACTGCTTCTTTCTTT | 10533 |
| rs572692210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11420052 | CATAGACTGACAGGT[C/T]CTTGTTCAAATTCTT | 10533 |
| rs572701465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11355514 | CAACTCCTACCACTC[A/G]AGACACACAAAGCAA | 10533 |
| rs572715187 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11529630 | CTGTGACCACCTGGC[G/T]CTTGAATACCACAGC | 10533 |
| rs572729544 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG7 | GRCh38.p7 | 3:11463284 | TTTGTAAGCTTGAGA[G/T]GACTCAGGTTGCTGA | 10533 |
| rs572743462 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11314437 | TGTTCGTACAAATCC[A/G]AGGTTGTGGTTTTGT | 10533 |
| rs572746400 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG7 | GRCh38.p7 | 3:11468656 | GAACTCTTGATCCCC[C/T]ACTACTTCATTCTTT | 10533 |
| rs572747318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11401905 | TGTTACAGTAAGAAA[C/T]GCATGTTTTAATTGG | 10533 |
| rs572808413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11481722 | ACAGGGCTTCAGCTC[C/G]TATCTTGAGACTTGG | 10533 |
| rs572812480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11522594 | TGGGAGGGGCTTGAA[C/G]CAGAAGGAATCGTGC | 10533 |
| rs572812507 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11353901 | ACTAACACAGGAAAT[A/G]CAAAGAAGTGTACCA | 10533 |
| rs572816241 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ATG7 | GRCh38.p7 | 3:11490176 | CTGTATTGGGTGCAT[A/G]TATATTTACGATAGT | 10533 |
| rs572816262 | snp | A/G | | | intron-variant | ATG7 | GRCh38.p7 | 3:11441060 | ATCTTATTGTTGCAG[A/G]ACAAAGTTGTTGAGT | 10533 |
| rs572821866 | in-del | -/A | | | intron-variant | ATG7 | GRCh38.p7 | 3:11278507 | TTTCTCAAACATACC[-/A]TCCTGGTTTGTTCTT | 10533 |
| rs572822207 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11476539 | CAGAGATAGAGTCCT[-/G]GCCTGAAAAGTGAGT | 10533 |
| rs572826563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11341144 | TCTGCTCACTGCAAC[C/T]TCTGCCTCCTGGGTT | 10533 |
| rs572827935 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG7 | GRCh38.p7 | 3:11318443 | GGTCTTCTATGCCTT[A/G]TCTTATTCTAGGAAA | 10533 |
| rs572840897 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | ATG7 | GRCh38.p7 | 3:11286924 | TTTATTATTATTATT[-/ATT]TTATTTTTAAATTAA | 10533 |
| rs572849630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG7 | GRCh38.p7 | 3:11528803 | TGCACTCCAGCATGG[A/G]CGACAGAGCAAGACT | 10533 |
| rs572870983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11486347 | GCTGTTTGTCTGTTA[C/T]TGCTGTATAAGAATG | 10533 |
| rs572871929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11362265 | TTAGAGCCATGTTGT[A/G]GAAAAAAAAAATACT | 10533 |
| rs572886814 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ATG7 | GRCh38.p7 | 3:11516748 | ATAAAAATAAATGAG[-/C]CTATCAAGCCATTAA | 10533 |
| rs572886851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11407888 | CAGGGCCTGTAGTGG[A/G]AGGGGCTGCCACAAA | 10533 |
| rs572903738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG7 | GRCh38.p7 | 3:11299840 | AGGCATTATAGTGCT[A/G]TATAAAGGAATATGA | 10533 |