SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs139785517 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106309639 | CCACAGGAAGTATTA[C/T]CGCCCCTGTTTTAAA | 9474 |
rs139804984 | snp | C/G | 0.162909 | 0.23434 | intron-variant | ATG5 | GRCh38.p7 | 6:106267543 | CCAAGACAATCCTAA[C/G]CAAAAAGAACGAAGC | 9474 |
rs139810362 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106188976 | TAGAATAGGGCAGCA[A/G]AAACTTCAAACCGAA | 9474 |
rs139829517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195346 | AATCTTAAAGTCTTT[C/T]GCTTTCAACTTAAGT | 9474 |
rs139861860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106311307 | TACAAATGTGATTAA[C/T]GCAGGGAGGAAGTAA | 9474 |
rs139870085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234742 | CTTCCTTTTGTTATC[A/G]GAGCAGGAGTGCTAG | 9474 |
rs139925730 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327665 | ATGATTGTATCACTG[C/T]AGTCTAGGTAACAGA | 9474 |
rs139927375 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106238487 | CCTTTCCTCCAAATT[C/T]CATCTCCTATTAACA | 9474 |
rs139947350 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ATG5 | GRCh38.p7 | 6:106253601 | GCAATTACTTCTCTC[C/T]GTGTTCACCACTACC | 9474 |
rs140020431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210050 | TTGAGAAGCACTAGT[C/T]TACAACAATGACTTT | 9474 |
rs140026982 | snp | C/T | 0.000710938 | 0.0188405 | utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316245 | ACATACAGGCTAAAT[C/T]CTTATTTCAACCAAA | 9474 |
rs140065845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106320950 | TGCCTGACCTAGAGA[A/G]GTAGTCATGGACTGG | 9474 |
rs140074803 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106196742 | AAAAAAAAAAGTAGA[C/T]TGAAAGTTCTACAGT | 9474 |
rs140114093 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106200979 | CAGGCTCAAGTCGCT[A/T]ATATAGAATGGCATA | 9474 |
rs140155066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204578 | TAATCCCCATGTGTC[A/G]AGGGAGGGAGGTGAT | 9474 |
rs140156517 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106270886 | CATCCTCTACATCCA[C/G]CCTAACAACAGGCTC | 9474 |
rs140176369 | in-del | -/AC | 0.222928 | 0.24853 | intron-variant | ATG5 | GRCh38.p7 | 6:106198107 | ACAAACACCCTTATA[-/AC]ACAGAGAAAATGAAC | 9474 |
rs140178532 | snp | A/G | 0.166506 | 0.235645 | intron-variant | ATG5 | GRCh38.p7 | 6:106264012 | ATGAATTGACAGAAG[A/G]AGGCTTCAGAAGGTG | 9474 |
rs140243308 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106251054 | CCCTCAAGACAGAAT[C/T]TAGCACTCCAAAGGC | 9474 |
rs140267586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313074 | AGTAAAATAAACAGA[C/G]AAGGCAGAGGTGGAG | 9474 |
rs140281895 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106207811 | AAAGAGTATTAGATT[C/T]GGCTGGGGGTGGTGG | 9474 |
rs140309828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277742 | TCGCTTGAACCTGGA[A/G]GGCAAAGGATGCAGT | 9474 |
rs140327997 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106281926 | TCCATGATGACTAAA[C/G]ATGTTGAGTGCCTTT | 9474 |
rs140348944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259142 | AAAACTGTTATATAA[A/C]AACTAATTCACTGCA | 9474 |
rs140349211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106240808 | ACTTGATAGTGAATA[C/T]TGAACAAATTACAGT | 9474 |
rs140368233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106245271 | CAGATGAAAAATAAA[C/T]AGTTTGATGACAATC | 9474 |
rs140432778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106306990 | AATGCTATAACAAGA[C/T]AACTGTGTCATAAAT | 9474 |
rs140434811 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106275937 | CAACGACAATACATA[A/C]GTGAATGAGTGTGGC | 9474 |
rs140450069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265129 | ACACATAGGTTCAAA[A/G]TAAAGAGATTGAGGA | 9474 |
rs140453512 | in-del | -/TAAT | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106323439 | GCCACTATGCCCAGC[-/TAAT]TTTTTATTTTTTTGT | 9474 |
rs140455408 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186397 | GTTGCCTTATCTGAC[A/G]TGGAATCTTTTTCCT | 9474 |
rs140535648 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106222449 | AAATTCCAGAATTTT[A/G]GCTGTTTCAATCTCT | 9474 |
rs140556702 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106260972 | TGTTTAAAAGCATGT[A/G]ACACCTGGAAATGCG | 9474 |
rs140632491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106298205 | ACCTCATGATCTGTC[C/T]GCCTCGGCCTCCCAA | 9474 |
rs140649747 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106301575 | CATTCATTCACTGAA[C/T]AAACATTTACTTATC | 9474 |
rs140653243 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106219108 | TAAACGAGCAGAATA[A/C]ATTCTTTTGTTTTAT | 9474 |
rs140655108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227580 | TTGCAGTGGAGACCC[C/T]GTCTCTATAAAGAAA | 9474 |
rs140729033 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | ATG5 | GRCh38.p7 | 6:106321677 | CTTAATCCTCTTAAG[A/T]GTCGGCTTAATATCA | 9474 |
rs140751020 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ATG5 | GRCh38.p7 | 6:106212522 | CGGGTGCTTGTAATC[C/T]CAGCTACTCGGGAGG | 9474 |
rs140766706 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106274959 | GAAAGTTGAAAGCAT[G/T]AACAGTTCTGCCTCC | 9474 |
rs140773145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201814 | ATAATTTACAAAATA[A/G]TATATTAAATATTAG | 9474 |
rs140801035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285781 | TAAATCTGTATTTCA[C/T]GCAATTTTCACGTCA | 9474 |
rs140865708 | snp | A/G/T | 0.00319098 | 0.0398384 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326767 | ATAAGGAAAATTCTA[A/G/T]TAGTAGCCACAGGAT | 9474 |
rs140900064 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293083 | GATGCAAGAAGATCA[A/G]ATAGCAAACCAATTG | 9474 |
rs140907340 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106279030 | AAACCATGATAACTG[A/C]AATTCATGCATACTG | 9474 |
rs140908791 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106281488 | TTGAGATTCATTCCT[A/G]TTACTACACATATCA | 9474 |
rs140916502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205268 | GACTGTACCCACAAC[C/T]CAAAGAAAAAAGTCA | 9474 |
rs140928223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106239474 | TATGGGGAACTGAAT[A/C]AGTGATTTTAAAAGT | 9474 |
rs140938322 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106302333 | TGGAAAGAAGTGGGA[A/T]CATGGACAACCTTTA | 9474 |
rs140942268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106319220 | AGGTTATCTACTATT[A/G]TAATTTACAGAACAA | 9474 |
rs140942705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228555 | GGCCAAGAACCCCAG[A/G]TCAGAGAACACGAGG | 9474 |
rs140949499 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106241148 | ACAGAACGAGACTCT[A/G]TCTCAACAAAAAGAA | 9474 |
rs140981868 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG5 | GRCh38.p7 | 6:106323420 | GCCAGGACTACAGGC[C/T]CATGCCACTATGCCC | 9474 |
rs140990253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245695 | AAATATTTCAGTAAA[A/T]ATTATGCCCTTTATT | 9474 |
rs141027602 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106250030 | ATATTTTCTCCCGTT[A/C]TGTACATTGTTTTTT | 9474 |
rs141029675 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106203307 | GACAGAGTACAGAGG[C/T]TCTGAAATGAGCCAG | 9474 |
rs141057376 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106189920 | AGTGAACTAGTTCTA[C/T]ATGAACTTCTTTATA | 9474 |
rs141068820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106206777 | CAAGTACAGAGGTTC[C/T]TAAGGGCAATGGGAA | 9474 |
rs141094430 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106286277 | TGAGCTCCACTCTCC[A/G]TACCACCGTCAGGCA | 9474 |
rs141107759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213034 | TGTTTAACAAAAGCA[C/T]AGGTACAACAACGAC | 9474 |
rs141121425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255353 | TTCACAATTGCTACA[C/T]CTTATTACAGCATAG | 9474 |
rs141136456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241258 | TTCAAGGATGATAAA[C/T]AAGCACATGAAAAGA | 9474 |
rs141137669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290032 | AGTTTATTATATTAT[C/T]ATTATTTTGAGACAG | 9474 |
rs141201435 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106304478 | TATAACCATACAGTG[A/G]GATACTCAGCAACTC | 9474 |
rs141245391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235919 | TTCAAGAGGACCCCT[C/T]CAACAAGATATTGGG | 9474 |
rs141339667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264636 | CATCAGACTAACAGC[A/G]GATCTCTCTGCAGAA | 9474 |
rs141346961 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG5 | GRCh38.p7 | 6:106298714 | CCATAATTAACATGC[A/G]GTTCAATACAAATTT | 9474 |
rs141380134 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106227181 | CTGAAATATAAAGAG[A/T]GACTCTCAAAACAGG | 9474 |
rs141488529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252449 | TTTATATTGGTCTTG[A/C]AAATTTTAAAACACC | 9474 |
rs141496914 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106270816 | TATAAAGCACCACTC[C/T]CCATGCAGCTGCCCA | 9474 |
rs141508940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209337 | CTGTCCCACGGAATA[A/C]TACTCAGCAATAAAA | 9474 |
rs141524533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106232941 | CTCAACTCACCTGGA[C/T]TGTTTCACCCCAAGG | 9474 |
rs141527648 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251165 | GCCCATCTGTGGTTT[-/C]CCCACCCAGCTGCCA | 9474 |
rs141544510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106200091 | TTCATTTTTAAAGCA[C/T]TACATACATGTAGGA | 9474 |
rs141558047 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273656 | AGTGACCTGCCATGA[C/T]CATACAACTGATAAG | 9474 |
rs141593318 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106324994 | AATCTAGAACCAATA[A/G]TTTCCTAGGTTCCTC | 9474 |
rs141602832 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106190846 | GTATATATTAAAAAA[C/T]GATGCTTACATATAG | 9474 |
rs141613830 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ATG5 | GRCh38.p7 | 6:106278640 | AACTCCATTTCTTTC[C/T]ATTCAAATTTCATTC | 9474 |
rs141618566 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106204101 | GGGCTAGGGGAGGGA[C/T]AGCATTAGGAGAAAT | 9474 |
rs141648980 | in-del | -/TAAA | 0.216649 | 0.247765 | intron-variant | ATG5 | GRCh38.p7 | 6:106240400 | TATAAAATAAAAAGT[-/TAAA]TAAGAAGAAAAGATA | 9474 |
rs141681436 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106267385 | TCATGGATAGGAAGA[A/G]TCAGTATCATGAAAA | 9474 |
rs141721964 | snp | A/C/G | 0.0248432 | 0.108648 | intron-variant | ATG5 | GRCh38.p7 | 6:106272656 | CCCTACACATTCAGA[A/C/G]GGAAGGGATCGTGCC | 9474 |
rs141730376 | in-del | -/TATTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290243 | TTTATTTTATTTATC[-/TATTT]TATTTTATTTTATTT | 9474 |
rs141730597 | in-del | -/A | 0.124976 | 0.216492 | intron-variant | ATG5 | GRCh38.p7 | 6:106274343 | AAAATGAAAACTCAT[-/A]AAAAAAACACTGAAA | 9474 |
rs141808345 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106221558 | GCGCCTGGTGGTGTG[A/C/T]GCCTGTAGTCCCAGC | 9474 |
rs141834176 | in-del | -/TTTATTTTAT | 0.496382 | 0.0423778 | intron-variant | ATG5 | GRCh38.p7 | 6:106290260 | TTTTATTTTATTTTA[-/TTTATTTTAT]TTTATTTTATTTTAT | 9474 |
rs141889130 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221720 | AGAAAGAAAAAAAAA[-/A]TCAAAACTGATCACT | 9474 |
rs141903612 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106291199 | TATGTGTACTTCCCA[C/T]TCCATCATACAGGAT | 9474 |
rs141908661 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106287845 | TTTAACTGTAATGTC[A/G]CTTTGCAAGCAGCAT | 9474 |
rs141928246 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106215568 | GATTTCACCACTTAC[A/G]TAATCTGATCAACAA | 9474 |
rs141929876 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106246887 | GACAAATGATAAATG[A/C]TTTAATAAATTAGAA | 9474 |
rs141951544 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261925 | ACAGCCCCAACCCTC[A/C]CAGCCACATCAAAGA | 9474 |
rs141959172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106292472 | TTTTTCAAAACAGAG[A/G]TAGATCAAATCTTTG | 9474 |
rs141966896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221230 | AAAAATAATATAAAC[C/T]AGGCAGTAGACTTAC | 9474 |
rs141973897 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106254319 | AAATTATGCAATTTA[A/C]ATGTTTAAGTATGTA | 9474 |
rs142087377 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106224875 | AAAAAGAGCGAAACT[C/G]TTGTCTCAAAAAACA | 9474 |
rs142126489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289289 | TATAAGGCAGTACAA[C/T]AGAGGCAGGCCTACA | 9474 |
rs142146106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106250442 | AAGGCCCAGATTATT[A/G]TATGTTTAATTAATA | 9474 |
rs142248278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106322128 | TGTGACGCAATCTAC[C/T]AGAAGTAAGTTTCTT | 9474 |
rs142273802 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106201817 | ATTTACAAAATAATA[C/T]ATTAAATATTAGGTG | 9474 |
rs142309579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106309063 | GAGTGTTTTGGAAAA[C/T]CAATTATGATTTATA | 9474 |
rs142310161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312723 | GGGCTAACAGGACAA[C/T]GCCACAAGATGGGAG | 9474 |
rs142330889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317547 | AATATGTCCAACATA[A/G]AAGTACTAGGCAACA | 9474 |
rs142330944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268708 | GCCATAAAAAAGAAT[G/T]ATTTTGTATCCTCTG | 9474 |
rs142349658 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106271889 | ATTAGTTCTCTGGAA[A/G]TGCCTAGAATATTCC | 9474 |
rs142354288 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106197168 | TATAAAAAAGGAAGT[A/T]TAAAACAACATATTT | 9474 |
rs142354756 | in-del | -/AAAGA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273615 | GGTAGAAAAGAAAAG[-/AAAGA]AAAGTCCAGCTTAGA | 9474 |
rs142358338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236198 | TAATCCTGAATAGTA[C/T]GCTGTTTTAGGAATA | 9474 |
rs142381028 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106315423 | ACAGAGGCATAAACT[A/G]GGATTATACATGCAC | 9474 |
rs142406615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196443 | AAGTGGTTAAGAGAC[A/G]TTTGGCACAATCATG | 9474 |
rs142451865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106300705 | CAACTGTAACACAAT[G/T]ATAAGTATGTATGCA | 9474 |
rs142454539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271064 | AGCTCTTATATCATA[C/T]TCTACATCTCATCAC | 9474 |
rs142455082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314181 | TTTTCCAATTTAAAC[A/G]GGTCTATAAAGAAAA | 9474 |
rs142501949 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106194772 | TAACTCCTGACCTCA[A/G]GTGATCCACCCGCCT | 9474 |
rs142579467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254245 | GGTAAGACAGTCCCA[C/T]TTTCCAATCATTCCC | 9474 |
rs142582611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226239 | ACTTTAGGGGCCTGT[A/G]TGATAAAAAATAAAA | 9474 |
rs142598786 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106211566 | ATAAAAAAAATTAGC[C/T]GGGAGTGGTGGCGTG | 9474 |
rs142730612 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106253037 | TATTGTTTTAATCAG[A/T]GGCTTTCAAGGTATG | 9474 |
rs142757538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106281025 | GTTATAGCCTACTCC[A/G]GTTACTGTATTCACA | 9474 |
rs142763937 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106206338 | CCGAATCTGTTGAAG[C/T]CTTGATCTCTGACTT | 9474 |
rs142768371 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ATG5 | GRCh38.p7 | 6:106256687 | ATGTGCAAACCAGGA[A/G]AAGGTACAGTAAAAA | 9474 |
rs142789625 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ATG5 | GRCh38.p7 | 6:106266624 | TCTGGCAAACCGAAT[C/G]CAGCAGCACATCAAA | 9474 |
rs142809758 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ATG5 | GRCh38.p7 | 6:106269696 | GCCGGCCGGCTGCTC[C/T]GAGTGCGGGGTCCGC | 9474 |
rs142822654 | in-del | -/TTTAT | 0.0644693 | 0.167566 | intron-variant | ATG5 | GRCh38.p7 | 6:106242562 | AAATTTTATGTTACA[-/TTTAT]TTTACCATGATTAAA | 9474 |
rs142878178 | snp | C/G | 8.33924e-05 | 0.00645672 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186672 | TTGATTCTTTTTTTC[C/G]CCATCTATTCCAAGA | 9474 |
rs142897720 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214697 | GCAAATTTTCTTCAA[A/G]TAAGCGCAACACTTT | 9474 |
rs142905381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273952 | TTTAAGTTAAAATGG[C/T]ACACTATCAAATAAT | 9474 |
rs142923738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106234210 | CTAGCCCCTACAAAG[A/G]ACTAGATCTCTTAAA | 9474 |
rs142936634 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106220407 | TAATAAAACCAAAAA[A/G]CAGGCATCACACACA | 9474 |
rs142937624 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106229823 | ACAGAAAAAAGTAGA[A/G]AAGTAACTTTTAGAG | 9474 |
rs142985032 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ATG5 | GRCh38.p7 | 6:106297388 | TCTAATTGGTGTTGA[G/T]TCACATAAAAAAGAA | 9474 |
rs143002170 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106282527 | AGTTAAGAACACATA[C/G/T]GATGCATTATGGAAG | 9474 |
rs143092817 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106315027 | TCATGCACCGAGTAG[C/T]ACCACTTGAGGAGCC | 9474 |
rs143138103 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106195740 | TACTCACCTACAGCA[A/C]CTGAAATCACCTAAA | 9474 |
rs143165380 | in-del | -/TGTA | 0.0584853 | 0.160693 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185872 | TAAAAAGTGATCTAC[-/TGTA]TGTGAGTCAGAAAGT | 9474 |
rs143175130 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106283705 | GGCATGTGCCACCGC[A/G]CCCGACTAGTTCTTA | 9474 |
rs143215439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106242067 | GCAAAATGTGGTATG[C/T]ATATACAATGGAATA | 9474 |
rs143217706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106287033 | GTTTTAAGCTGGTGG[C/T]AATTTGTCAGACAAT | 9474 |
rs143282506 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106306753 | CCCACACTGTTTCCC[C/T]GTCCATCCTGTCATT | 9474 |
rs143296669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292236 | AATATAAGAGACCGA[C/T]ATGGTGGAATCATTG | 9474 |
rs143306121 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186317 | GGTAAGTCTTTCATG[G/T]CACAGCTGAGGTTTA | 9474 |
rs143317248 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ATG5 | GRCh38.p7 | 6:106251998 | GGCATGCATCATCAC[A/G]CCCGGCTAATTTTTG | 9474 |
rs143358145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106246566 | TGTACACATGCACTA[C/T]ATTCTGACAATAATA | 9474 |
rs143469353 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106324159 | TTCTTCGTCCTTGTA[G/T]TCAACCAATCATGGA | 9474 |
rs143471877 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106281580 | TATCTAAAAACTTGT[A/T]AATAGACACTGGGAT | 9474 |
rs143483680 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106207169 | TTAGTCATTTCTTAA[C/T]ACCAAATGAAATGAA | 9474 |
rs143494459 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106204019 | ACTCACAACTGGGAG[C/G]TGAACAACGAGAACA | 9474 |
rs143508570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284732 | GGGTTTTTTTTGTTT[C/T]TTTTTTTTGCTTTTC | 9474 |
rs143520772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210346 | ATAACAGAGCAAAGG[C/T]AATTATTACAATGTA | 9474 |
rs143576190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318843 | TAAATTATATAAGAA[A/T]GCATGTCTCCAGTGA | 9474 |
rs143595063 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106272161 | GGTATAGACCACTGG[A/T]CTGATATGACCACTG | 9474 |
rs143600303 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ATG5 | GRCh38.p7 | 6:106197961 | GTGCTGCCACGGACA[A/G]GTAAGAGGTTTATGG | 9474 |
rs143630322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261869 | CTGGCATCTAGTCTG[C/T]AGAGGCCAGAAGTGC | 9474 |
rs143703326 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106268467 | TTGTGGAACAGTGTG[A/G]CAATTCCTCAAGGAT | 9474 |
rs143769620 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ATG5 | GRCh38.p7 | 6:106265816 | GAAAAAAGAGACAAC[A/G]TACCAGAATCTCTGA | 9474 |
rs143781161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106186782 | AATGGATTTTAAACA[C/T]GTTTTGTCCCCTGAA | 9474 |
rs143790520 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106287113 | CCAACATTTATAGCT[A/G]GGAAGTGCAGGCAGT | 9474 |
rs143898306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227256 | CTCATCAGAAATGAT[A/G]TTGTCAATAGGCAAT | 9474 |
rs143928564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305015 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 9474 |
rs143940748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106270503 | TAAATGAGGTGGCTC[C/T]ATATTTCATTGCTTT | 9474 |
rs143974206 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184320 | TTACTATTAGTCAAA[C/T]AGGCATATTGGGGGT | 9474 |
rs143993702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188560 | GGTAAACAATCCACT[A/G]ATGATGCACAGTGTA | 9474 |
rs144002295 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106204935 | ATCATGCATAATCAA[C/G]TGATTAACTGTGTAA | 9474 |
rs144133439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106283600 | TGCTGAACTTAGTGT[A/G]GAAATTCAATCGGCA | 9474 |
rs144145329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208334 | AAAATGCACAACACA[A/G]TTCTGACACATAACA | 9474 |
rs144146871 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106245424 | TAATGATTACAAACA[A/G]AAGTCATAGTTTGCT | 9474 |
rs144147227 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106288640 | TCAACATGTGGTCTG[A/C/G]TGGAACAATATCATA | 9474 |
rs144154229 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ATG5 | GRCh38.p7 | 6:106298464 | GCTGAAGTGGGAGAA[C/T]TGCTTGAACCCGGGA | 9474 |
rs144166574 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106249349 | AATGAAGTAATATAA[C/T]ATGTGGTTCTTTTGC | 9474 |
rs144250157 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106261112 | TTAGAGTTAAAGAGT[-/G]GGGAAAGAAGAGTTG | 9474 |
rs144254313 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106284276 | TCCAAAAAGGCTACA[C/T]CATTTTACATTCTCA | 9474 |
rs144264853 | in-del | -/ATAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240403 | AAAATAAAAAGTTAA[-/ATAA]GAAGAAAAGATAGGC | 9474 |
rs144273987 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106243773 | GAGGCGGAGGTTTCA[A/G]TGAGCCGAGATTGCA | 9474 |
rs144342112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106217855 | TGAATCCAAAGTAGG[C/T]TGATACATCCCAACA | 9474 |
rs144353459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305340 | AAAAAACAAAGCCCC[C/T]GGTACTCTTCATCTA | 9474 |
rs144376736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106315097 | AAAAAAACAGTCCTA[C/T]ACCCAAAAAGTGAGC | 9474 |
rs144379560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237716 | AAATCCAGTCCCGAA[C/T]TCCATAAAATGTATG | 9474 |
rs144400614 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106196223 | AGCATGTAGGCAGAT[C/T]AGATACTAAACACAA | 9474 |
rs144401210 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184925 | TCATATTCAGACCAG[C/T]CTCTTGTGCAAAAAT | 9474 |
rs144432567 | in-del | -/CAA | 0.0482946 | 0.147699 | intron-variant | ATG5 | GRCh38.p7 | 6:106322215 | AGAGTAGGTGCCCAC[-/CAA]CAACATCTGTTAACC | 9474 |
rs144484144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308309 | TTTCAGGGCACTATA[A/C]CTTTTTAAAGCTAGT | 9474 |
rs144498650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294330 | TATCAGTTAATATTA[C/T]TTATGCTTGTGCTAC | 9474 |
rs144499155 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106310156 | TTCCACTGCCCAAAA[C/T]AGTGCCTGCTTTAAA | 9474 |
rs144502925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266794 | AGGCCTTAGGTAAAA[C/T]TCAACATCCCTTCAT | 9474 |
rs144506815 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106188246 | ATAAGTTCCAGTTTG[C/T]TAAAGCTTTACTGTA | 9474 |
rs144546416 | snp | C/T | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106229576 | AAAAAAAACAGTGTG[C/T]CCTATTCCTTTAAAA | 9474 |
rs144549061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189044 | GCATGGTACCTGACA[C/T]ATACAGTAATTAGAT | 9474 |
rs144628562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261634 | ACTGCTACTTTAAAT[A/G]AGAAGCAGTTTTACC | 9474 |
rs144653646 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106319481 | ATTAACAAAGTATAA[C/T]CTCCAAATCTACTAA | 9474 |
rs144653986 | snp | C/G | 0.096847 | 0.198299 | intron-variant | ATG5 | GRCh38.p7 | 6:106221462 | AGGCCAAGATGGGCG[C/G]ATCACTTGAGCCCAG | 9474 |
rs144692780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323753 | TGCATACAGTCAACA[C/T]AGCAATCAGATCTTT | 9474 |
rs144697652 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327240 | GATGGATTTAGGGGC[A/G]CATAGATGGATAAAT | 9474 |
rs144700317 | snp | C/T | 0.0252474 | 0.109482 | intron-variant | ATG5 | GRCh38.p7 | 6:106199813 | GTTTCATGGTAATGA[C/T]AGAAAGAATTCAGTA | 9474 |
rs144702940 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106247750 | TGGCACTACATACAC[C/T]GTGACAAGAAGGCTT | 9474 |
rs144723807 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | ATG5 | GRCh38.p7 | 6:106205718 | CCCAAATCTGAGCAA[C/G]TATTATAAAGGTATA | 9474 |
rs144730561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276733 | ATTATTAACTTCAAT[C/T]GTGAAGTTAACTCAA | 9474 |
rs144736938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106203713 | AGCCTCCAGAGTAGC[C/T]GGGACTACAGGTGTG | 9474 |
rs144750172 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ATG5 | GRCh38.p7 | 6:106279556 | CACAGAGGCTACAAT[G/T]TAAACTTGTACCACC | 9474 |
rs144791134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106237883 | ATAAAGACATAAGCA[C/T]AGTACAGAGCCTTAG | 9474 |
rs144806907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106320893 | TGAGTCAGAGAGGCT[A/T]GCCAGGTAGTAATTT | 9474 |
rs144827026 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106273882 | TATTTTCCAAATGTC[A/G]TGACTTGTTATAAAA | 9474 |
rs144832309 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106200801 | GCAATTTTTATGTCA[A/G]TACAGTAATATGCCA | 9474 |
rs144842037 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220276 | TCAATATAATCAATG[A/C]ACACAACAATACGTA | 9474 |
rs144915225 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106223625 | ATGATTATCATTCAC[C/G]CATTCACTATAGGAG | 9474 |
rs144983689 | in-del | -/ACAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312624 | CTGGCAAAAAAGACT[-/ACAC]ACACACACACACACA | 9474 |
rs145028559 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288985 | TTAGAAGCTTTGATA[C/T]TGCACAAAAAAATCT | 9474 |
rs145034654 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106217369 | GTTTAAAAAGGTTTA[C/T]TAAAATACATAATTT | 9474 |
rs145047681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261431 | GCCAAATAAGTCATT[A/G]TGACAACAGGACATA | 9474 |
rs145060025 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ATG5 | GRCh38.p7 | 6:106276369 | TTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA | 9474 |
rs145067694 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | ATG5 | GRCh38.p7 | 6:106264712 | TTAAAGAAAAGAATT[G/T]TCAACCCAGAATTTC | 9474 |
rs145088158 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106224604 | AATACGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 9474 |
rs145095968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235454 | CCAACCTCCCCAACA[C/G]CACTTGGGTTTTCCT | 9474 |
rs145123891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296305 | ATATATTTTAGGGTC[G/T]TAATGATCTTATTGT | 9474 |
rs145164283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299404 | TCAATCCATGGTTGG[C/T]TGAATCCATGGATGC | 9474 |
rs145198178 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ATG5 | GRCh38.p7 | 6:106258331 | TGAGCCATGACCTTA[C/T]CACTGCATCTTAGCC | 9474 |
rs145320838 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241921 | TCTCTCTCTACACAA[-/AC]ACACACACACACTAC | 9474 |
rs145367455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282130 | AGCTAGGAAAACATA[A/C]AATGCACACATGTGC | 9474 |
rs145369559 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106235966 | TAAAAGTTCCTTCTT[C/G]TCCCTTACTGGTTGG | 9474 |
rs145408727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106300125 | AATCTATGTAAGTCA[C/T]ATTTCAAAAATCTAG | 9474 |
rs145409122 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106240912 | AATCCCAGCACTTTG[A/G]GAGGCCAAAGCAGGC | 9474 |
rs145438411 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316528 | AAGTACTGAACCACA[C/G]TCAAAATGAAACTGT | 9474 |
rs145446102 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106238543 | TCCTGGGGTTGGGGA[A/G]GGGTGTACATGGAGA | 9474 |
rs145468794 | in-del | -/AT | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106273176 | CAGTTCTACTTAGGA[-/AT]CTACTTTTACACCAC | 9474 |
rs145476582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106286118 | CATGTGCAACCCAGG[C/T]CTCAGCCAAGCACCC | 9474 |
rs145485594 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242574 | ACATTTATTTTACCA[A/G/T]GATTAAAAATTAAAA | 9474 |
rs145485614 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106197023 | CTTATATAAACTTGG[A/G]ACTAGCAAATATGGA | 9474 |
rs145524494 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106201053 | ATCTCTAGATTACTT[A/G]TAATATTTAATGCAA | 9474 |
rs145535496 | in-del | -/ACACACACACAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312624 | CTGGCAAAAAAGACT[-/ACACACACACAC]ACACACACACACACA | 9474 |
rs145596648 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106318274 | TAAACCAAAACATCA[A/T]GCATGTGAGTGTGGC | 9474 |
rs145602566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106240079 | CTCACTGCAGCCTCA[A/G]CCTCCCAGGTTCAAG | 9474 |
rs145618695 | in-del | -/TTCT | 0.0372196 | 0.131242 | intron-variant | ATG5 | GRCh38.p7 | 6:106305545 | AAACATCAATTTCTG[-/TTCT]TTCTTCCCTCACTTA | 9474 |
rs145623033 | in-del | -/TC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246436 | CACACACACACCCTT[-/TC]TCTCTCTCTCTCTCT | 9474 |
rs145634135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106197418 | TTCATTTACTCCTAA[C/T]TGATAAAATCATTTG | 9474 |
rs145682406 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298351 | TGGCATATTAAGAAT[C/T]AGGAGATAAATTTAA | 9474 |
rs145709082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301884 | CATTATCATTGCTGT[C/T]TTACAGACAAGAAAA | 9474 |
rs145713363 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106255844 | CAGAGCTACAGCACA[A/G]TGGTAGGCCAGGACT | 9474 |
rs145722476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106254451 | CTATGAGTATGCACA[C/T]AGTACATACTCAACG | 9474 |
rs145748181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261136 | AGAGTTGTTAAAATA[C/T]GCAGAGATAGATCAA | 9474 |
rs145762102 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106268240 | GAGCAGGCACTTCTC[A/T]AAAGAAGACATTTAT | 9474 |
rs145858691 | in-del | -/GA | 0.115088 | 0.210473 | intron-variant | ATG5 | GRCh38.p7 | 6:106227572 | CTCTTGCAGTGGAGA[-/GA]CCCTGTCTCTATAAA | 9474 |
rs145866305 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106212885 | AGCATACTATGGTAC[A/G]TTACTTTAGAGAATC | 9474 |
rs145868506 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106263808 | CATCAACATAAAGGA[A/C]CCCCACAAAAAAACT | 9474 |
rs145922719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106236321 | ATGTTTTCTCGGACA[C/T]ATATTTTCATTTTTC | 9474 |
rs145922831 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106188764 | ACTTTTAATTTTTAA[C/T]ATAAAAGCATCACTA | 9474 |
rs145951139 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246435 | ACACACACACACCCT[C/T]TCTCTCTCTCTCTCT | 9474 |
rs145951868 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106314322 | GGCATTTTGGAAGGC[C/T]GAGGCGGGCAGATCA | 9474 |
rs145965813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195058 | GACTAATTCCCTTAG[C/T]CATTTACAAAAAAAG | 9474 |
rs146034033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106253421 | AATCTGTGGTTTCAG[C/T]GAATCACAAAAGCAA | 9474 |
rs146047716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307797 | AGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTCGT | 9474 |
rs146075787 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106256726 | AAAATATTTTTAAAA[A/G]GCACCCCTGTATAGT | 9474 |
rs146076990 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106209875 | AAAATTTCAAAACAA[C/T]TAGTCTAGAGCTTTG | 9474 |
rs146087962 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106215067 | AGACTAATACAAAAA[C/G]AATGTAATTAATAAA | 9474 |
rs146118869 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106312751 | GAGAAGCAACCAACA[A/T]CATCAAACACTGCTG | 9474 |
rs146141455 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | ATG5 | GRCh38.p7 | 6:106195501 | ATTTTTAAATGACAA[-/T]TTTTTTTAATACGTA | 9474 |
rs146182438 | in-del | -/ACCCAGCAATTCT | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106216226 | TGGAATTACCATGCA[-/ACCCAGCAATTCT]ACTCCTAAGTATCTA | 9474 |
rs146208125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233593 | GTGGCAAAGGGTTGG[C/T]CTCATTGTTTATGGG | 9474 |
rs146217828 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106192386 | CTTTCTCATCCCAAT[C/T]TGGGTTTTAGGTCTT | 9474 |
rs146275719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288292 | ATTTTTCTAATATAT[A/G]TTTAAATTTTTTAAT | 9474 |
rs146283302 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106271971 | CCCAGATAAATATGC[A/G]TGATCTCCTAAACTG | 9474 |
rs146316011 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106292550 | GAATTACTCAACAGT[A/G]TTAGGTTGTCCCCTC | 9474 |
rs146327506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252772 | AGGAAACCGATGAAA[C/T]GGTCTCCACATGCAT | 9474 |
rs146394906 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106309406 | GGTAGGAGAACGTGA[C/T]ATTGATCCTAGGGGC | 9474 |
rs146398144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233773 | GTAAATCCCCATGGC[C/T]CTCCCTTATCATATT | 9474 |
rs146447159 | in-del | -/AAAT | 0.161596 | 0.233848 | intron-variant | ATG5 | GRCh38.p7 | 6:106298559 | CCATCTCCATAAAAA[-/AAAT]AAATAAAGTATTAAC | 9474 |
rs146497953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245443 | TCATAGTTTGCTCAT[A/C]AATCAGGCCTAGGTC | 9474 |
rs146508531 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327584 | CATGCGCCTACAGTC[C/G]CAGCTACTCCAGTGG | 9474 |
rs146510385 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106203232 | TAATAATCTCATTGT[G/T]TTACTCTTAAAATTG | 9474 |
rs146510684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106249570 | TTGTAAACACATTTT[C/T]GTGTGGACATATGTT | 9474 |
rs146520493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206574 | AGAATCACTTGAACC[C/T]AGAAGGCAGAGGTTG | 9474 |
rs146541555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232378 | TAATTATGCCTGAAA[G/T]CCCAACTCCCTTGTT | 9474 |
rs146565553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106302061 | TATAGGAAGTACACA[C/T]GTAGTGTAGAGATGG | 9474 |
rs146606201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306178 | AAGGGATAAATACTG[A/G]CAAAGTAAGAACATG | 9474 |
rs146617176 | snp | A/C | 0.166506 | 0.235645 | intron-variant | ATG5 | GRCh38.p7 | 6:106264013 | TGAATTGACAGAAGA[A/C]GGCTTCAGAAGGTGG | 9474 |
rs146628496 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ATG5 | GRCh38.p7 | 6:106267596 | TTCAAACTATATTAC[A/G]AGGCCACAGTAACCA | 9474 |
rs146638539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106227064 | TGGCCCTAAACTTCC[C/T]GAACTTGACCCCAAA | 9474 |
rs146683865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323945 | AACTAGCTAGTATGC[A/G]CCTGCTTCAGGGCTT | 9474 |
rs146735895 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106281902 | CTCTTTGTGGTTTTA[A/T]TTTACATTTCCATGA | 9474 |
rs146739112 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106207324 | AGAAAAGCAGAAAAA[C/T]GAAACTTATAAACAT | 9474 |
rs146746658 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ATG5 | GRCh38.p7 | 6:106284839 | GAATCCTTTGACTAA[C/T]TTTTAATTGGGTTTC | 9474 |
rs146750289 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106210406 | AAAATCACTAAGCAC[A/T]TAATGAAAATCCTTT | 9474 |
rs146857927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106300706 | AACTGTAACACAATG[A/G]TAAGTATGTATGCAT | 9474 |
rs146868184 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106305069 | GCACTCCAGCCTGGG[C/T]GACAAGAGCAAAACT | 9474 |
rs146871812 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106231748 | AGTCTGCCTTAGGCC[C/T]GGAACAAAACTTAGA | 9474 |
rs146898563 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106283605 | AACTTAGTGTGGAAA[G/T]TCAATCGGCATAGCA | 9474 |
rs146908694 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106286825 | AGAAGATAGGCCCCT[C/G]AATCCTACAACCATA | 9474 |
rs146911181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106213057 | ACAACGACTACTACT[A/G]CTAACATATAAGTAG | 9474 |
rs146921483 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ATG5 | GRCh38.p7 | 6:106218699 | TATGAATGCTGCAAT[A/T]CATAAGCAGACGTCA | 9474 |
rs147005049 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106303494 | CAAACACTTAAAGAA[C/T]TGACAGCATTTTTAC | 9474 |
rs147013534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106307693 | AGGCATGTGCCACCA[C/T]GCCCAACTAATTTTG | 9474 |
rs147016608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106232981 | TAGCCCCCATCTATT[C/T]GGCCAGGCATTAGCC | 9474 |
rs147025713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235399 | TGCACAACCCCTACT[A/G]TGCCCCAATTCCGCA | 9474 |
rs147026203 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186430 | CTGGCTTGCAGCAGC[A/G]AAGTGTTTCTGGTCA | 9474 |
rs147061737 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106191564 | TCTGTTTCCTCATCT[C/T]ACAGTGTGAACAAAG | 9474 |
rs147119436 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106251834 | AAGTGTCTTTCACAA[G/T]GGATTTTTTTGTTCC | 9474 |
rs147168449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304111 | CTAGAACTAGTGTGT[C/G]AGTTCAGCAAGGTTG | 9474 |
rs147214742 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG5 | GRCh38.p7 | 6:106266011 | AGAGCAGAATTGAAG[A/G]AGATGGAGACATGAA | 9474 |
rs147216771 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106186966 | TTAATGAAACTGTAG[A/T]GGCAAAAACAGCCCA | 9474 |
rs147264372 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ATG5 | GRCh38.p7 | 6:106321513 | ACAGGCGCCCGCCAC[C/G]GCGCCAAGCTAATTT | 9474 |
rs147273505 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326104 | TTCCTGGCATCACAC[A/G]ACAGTATTAATAAAA | 9474 |
rs147274628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274588 | AAAGGTTTAATATCT[C/T]TGACTTCACAAATTA | 9474 |
rs147286577 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106204975 | GGTTGAGGAGTTCAG[A/G]GAAGAAAAGAAATGA | 9474 |
rs147323069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106208963 | TTAAAGAAATGCAAA[C/T]TAAAACCACAATGTG | 9474 |
rs147323588 | in-del | -/CT | 0.0711525 | 0.174681 | intron-variant | ATG5 | GRCh38.p7 | 6:106322952 | TGAGACGGGGTCTCG[-/CT]CTGTCGCCCAGGCTG | 9474 |
rs147387557 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106192977 | GCCACGGAGGTAATA[C/G]TCAGCGAGGTCAGGT | 9474 |
rs147391923 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106226013 | CTCAAAAAACATCTA[C/T]GAAGGCCCTAAACTC | 9474 |
rs147416002 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106298847 | TTCAACACAATCTAT[A/G]AAAGAAAACAGAACT | 9474 |
rs147427490 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106230229 | CAGCCAAGCCTTAAC[A/G]TACTTACCGAATCAA | 9474 |
rs147476259 | snp | A/G | 0.00266083 | 0.0363777 | intron-variant | ATG5 | GRCh38.p7 | 6:106279865 | AAACAGGATACACAC[A/G]TTACAAAATTAACCT | 9474 |
rs147486548 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106283749 | CTTCACCAATGAAAC[A/G]ATCTGTGCAGGGTGT | 9474 |
rs147512766 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106224546 | GAAGTAGATTGGTGG[A/G]ACCAGTTAGAACCTC | 9474 |
rs147532513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246680 | CAGAACTTGACCCAA[A/G]TAAGTGCTGAGAGGT | 9474 |
rs147571676 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ATG5 | GRCh38.p7 | 6:106251320 | GCTGAATATACCTCC[C/T]CCAGTGAAGTCTGAG | 9474 |
rs147581768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254310 | CGTTACTTCAAATTA[C/T]GCAATTTACATGTTT | 9474 |
rs147641218 | snp | C/T | 0.000115926 | 0.00761245 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279778 | TAAAATGAGCTTCAA[C/T]TGCATCCTTAGATGG | 9474 |
rs147675962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317516 | TACAGGTACGTAAAC[C/T]GCAAGAGGTGGAAAA | 9474 |
rs147686020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271508 | AGGCACCTTCCTCTT[G/T]GACTCTCTAGCCGCT | 9474 |
rs147687871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106197082 | CTGTTAGGGGACAGA[C/T]CATTACAGAACACAT | 9474 |
rs147697442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106201431 | AAAATTTGTCCCTTG[C/T]TTGCAGGAAAACAGC | 9474 |
rs147745500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254692 | TAAGTGTTTCCTATT[A/G]TCATTATCTTTTAGG | 9474 |
rs147750476 | in-del | -/T | 0.0744748 | 0.178019 | intron-variant | ATG5 | GRCh38.p7 | 6:106250064 | TTTTTAAGCAACTCC[-/T]TTTTTTTTAACTCAC | 9474 |
rs147782181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260106 | ACACTGAGGCCTGTC[A/G]GTGGGTGGGGGCCTG | 9474 |
rs147791455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218112 | TGGTAAGGGGTTGAG[A/T]AAGGAGCATTCTGTG | 9474 |
rs147801226 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106223353 | TCCAATAAAGCTGGA[A/G]GAGGAAGGGGAAAAA | 9474 |
rs147816294 | snp | A/G/T | 0.00143465 | 0.0267448 | synonymous-codon, missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106248215 | ATTCCATGAGTTTCC[A/G/T]ATTGATGGCCCAAAA | 9474 |
rs147845413 | in-del | -/TTTTCT | 0.16846 | 0.236329 | intron-variant | ATG5 | GRCh38.p7 | 6:106194529 | ATATACCATTTTTTC[-/TTTTCT]TTTTCTTTTTCTTTT | 9474 |
rs147860148 | in-del | -/TGTG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201276 | GTATTCAAGTGTATA[-/TGTG]TGTGTGTGTGTGTGT | 9474 |
rs147876241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271976 | ATAAATATGCATGAT[C/G]TCCTAAACTGCTTCA | 9474 |
rs147886272 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275762 | AATGTGTAACATTTT[C/G]AGTCAGACTTCAGGT | 9474 |
rs147896663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106235181 | GCTCTAATATTGATA[C/T]TCCTCTTTGGACCCT | 9474 |
rs147906658 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106238287 | GGTTCAAGTGAACAA[A/C]TCATACTTTTAAGCA | 9474 |
rs147978424 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106324261 | CTAAACAATACACCA[A/T]AACAACTATTTATAC | 9474 |
rs147990588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204075 | CACACCAAGGCCTGT[C/T]GGGGAGTAGGGGGCT | 9474 |
rs148041695 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106272315 | GTTTCACTGGTCTCC[C/T]ACCATCCCACTCTCT | 9474 |
rs148049267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261744 | TGAAAAGTCAATAAA[C/T]AGGGGTTTATTTTGG | 9474 |
rs148105988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106228206 | TAAATCTTGCAACTG[C/T]ACTCTTCTGGTCCGT | 9474 |
rs148138229 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106287626 | AACACCAAGGTTTTA[C/T]AGGATTTGTTTACTC | 9474 |
rs148139813 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106213801 | AGGAAAACTTATCTT[C/T]GAACAATTGATGTGA | 9474 |
rs148192581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106283106 | TACACGGATTGAGAT[C/T]TGAATGTTGAATCAA | 9474 |
rs148202365 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106241219 | CCAATTCAAAAATGG[A/G]CAAAGGACTTGAATA | 9474 |
rs148254047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106312842 | TGACTTTGGCAAGAA[C/T]AGTTTTCTTGGAATA | 9474 |
rs148255429 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106235824 | ACTGCAAAAAAAAAA[C/T]AGCTTAATTGAAGAA | 9474 |
rs148260931 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106298616 | AAAATGAATAATCAT[C/T]CTGTTATGATTTTTT | 9474 |
rs148265417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192417 | ATTCAACTAAGCCAA[C/T]TTCAACAAGGAATAT | 9474 |
rs148316514 | snp | C/T | 0.161267 | 0.233723 | intron-variant | ATG5 | GRCh38.p7 | 6:106264755 | ACTAAGCTTCATAAG[C/T]GAAGGAGAAATAGAA | 9474 |
rs148318473 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186337 | GCTGAGGTTTAATGA[C/T]GGCAGTGGAGGAAAG | 9474 |
rs148359183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209317 | ATAAACTGACTGTAA[C/T]AGGTCTGTCCCACGG | 9474 |
rs148417179 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG5 | GRCh38.p7 | 6:106267290 | CCAACTTACAAGTGA[C/T]ATGAAGGACCTCTTC | 9474 |
rs148420103 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106188465 | TGTATACTATGAAAC[A/G]GCAGAAGAAACAAGT | 9474 |
rs148452014 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254210 | GTTACCCCCTCAGAA[A/C]GATTTCTTTCATAAT | 9474 |
rs148502742 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327299 | AATGGTAGAATATAA[C/T]GGTAAAATATAATGG | 9474 |
rs148512824 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106280475 | GCTTACTATAAGTCA[A/G]TTAGACCTCAATAAA | 9474 |
rs148514586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106206121 | GAAACCTATTCCTCA[C/T]CATGGCAGTATTAAG | 9474 |
rs148565473 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106273901 | CTTGTTATAAAATTA[A/C]CATTAGCTAATCACC | 9474 |
rs148574584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106234138 | GAGTTCAAGATCAGG[C/G]AAGAGAAAAACATGT | 9474 |
rs148625123 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106304182 | TGAACATTCACGCTC[A/G]TTTTGGCAGCACATG | 9474 |
rs148655072 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106284327 | AATTAACCTATACCC[-/T]TCTCCATCATGTGTT | 9474 |
rs148658967 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106289032 | AACCTTTGAAAACAA[C/T]TGTAAAAGAAATTCT | 9474 |
rs148661918 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106217697 | AACAATGTTATAAAT[A/C]CAGGTCAGAGTTTAT | 9474 |
rs148712657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284630 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 9474 |
rs148715583 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106256908 | AACTTAAGCTTACTA[C/T]AGCTTTTTCACTTTA | 9474 |
rs148722763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244581 | CCTCCCAAACTAGAA[C/T]AAATTCTTCCTGGGG | 9474 |
rs148775364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106315165 | TGACTTTCCGTAGCT[A/G]GAGCAGGCTGAGGAG | 9474 |
rs148787092 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106196335 | AAAAGTTAAAAAGAA[A/G]GAAAACAAAAACAAA | 9474 |
rs148819640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106260197 | AACCAACATGGCACA[C/T]GTATACTTATGTAAC | 9474 |
rs148823945 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106324002 | CCTTCTTTATCACCC[A/G]TAGGCCTCCAAGTTA | 9474 |
rs148827159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246000 | AGACTGAATACCAAA[C/T]AGGGAAATAGGAAAA | 9474 |
rs148877741 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106318602 | CCCATATACCATTGT[G/T]GCTTACATGTATATT | 9474 |
rs148882523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210759 | ATTGTATCATCTATA[A/C]AATGAGGATATTAAC | 9474 |
rs148890432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197916 | AAAGGGAAAAAAACA[C/T]AATACAGAGAAATGA | 9474 |
rs148966813 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106268259 | GAAGACATTTATGTG[A/G]CAAACAAACATGAAA | 9474 |
rs149019436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106264002 | AATGAAGTTGATGAA[C/T]TGACAGAAGAAGGCT | 9474 |
rs149029853 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106223694 | GAAATGAAACAATCC[C/T]TGTCCTTGAGGAATT | 9474 |
rs149037343 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106207882 | GAGGATCACGAGGTC[A/G]GGAGTCCGAGACCAG | 9474 |
rs149088967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276669 | TCTTTTTAACAGACT[C/G]AGCCATTCACAATAG | 9474 |
rs149124673 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106235479 | TTTCCTGTTGAGTGG[A/G]GGGACTGAGAGACAG | 9474 |
rs149183233 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106292027 | ATGAATGGACACCCC[A/G]ATGGGAAAGAAACTC | 9474 |
rs149188382 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186190 | TCACCTTAGGAAATA[C/T]CCCTGTTTATTTGTT | 9474 |
rs149230627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300132 | GTAAGTCACATTTCA[A/G]AAATCTAGTTTACAG | 9474 |
rs149262842 | in-del | -/TTAG | 0.160938 | 0.233598 | intron-variant | ATG5 | GRCh38.p7 | 6:106240512 | AGTGTGAGAGAATTA[-/TTAG]TTAAAGTAAAAATAT | 9474 |
rs149280367 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106308109 | AATAGCCCATAACCA[A/C]ATATATTCTTATTGT | 9474 |
rs149282411 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106233575 | AGTAAGGAAATTGAT[A/G]TAGTGGCAAAGGGTT | 9474 |
rs149284209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106203781 | GAAGGGGGTCTCACT[A/G]TGTTGCCCAGGCTGC | 9474 |
rs149292022 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106188139 | ATATACAGAATACTA[C/T]AGAAAGCATAGTACC | 9474 |
rs149334007 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106302981 | ATGGTAAATTTTGTT[A/G]CATGCATTTTACTAC | 9474 |
rs149343558 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106261586 | ACCCAGAACAGAACT[C/T]GGAATGAGTTAAAAT | 9474 |
rs149374945 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326949 | TCACACATGTAAAGG[A/G]TAAATATTGTGTCCC | 9474 |
rs149397717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106255634 | AACCAATTAAGAATA[A/G]TTTATTTCAAATGTA | 9474 |
rs149407623 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106213438 | TGCTAATTGTGGTAG[A/G]AAGTAAAATATTACA | 9474 |
rs149429522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320889 | GCCTTGAGTCAGAGA[A/G]GCTAGCCAGGTAGTA | 9474 |
rs149439304 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273835 | AGCTGGAACGGCTGC[A/G]TTTAACTTTTATGTT | 9474 |
rs149493089 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ATG5 | GRCh38.p7 | 6:106270438 | GGCAAATAATAATAA[C/T]AACAAAAATGACCTA | 9474 |
rs149503427 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106230562 | GTGGTTACACACCCC[A/G]GAAAGGAATAAGCAT | 9474 |
rs149514058 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282862 | CACAATCACACCTTA[C/T]TGCAGCCTCAACCTC | 9474 |
rs149556656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225460 | TTTTATATTTTATAA[A/G]TAATTAGAAAGAATA | 9474 |
rs149615283 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106278939 | AAAGTTTGCATTTTA[C/T]GTAATTATCTGCGGT | 9474 |
rs149616923 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ATG5 | GRCh38.p7 | 6:106251850 | GGATTTTTTTGTTCC[C/T]TTTAAAAAGAGACAG | 9474 |
rs149655399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106299754 | GGACATGATTCTAGT[A/G]TAAATATCTGTACTC | 9474 |
rs149657771 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106226898 | CAGCAAATCTAAAGA[C/T]AGGTCAATTGCGAGA | 9474 |
rs149744617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253746 | ATTTTCAAATATTTT[A/C]TAATGGGCCATAAAA | 9474 |
rs149751129 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318170 | CTTCCCTCCTCTTCA[A/G]GCACTGTCCTCTCAA | 9474 |
rs149772753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106247717 | ATCACTAATAAAAAG[C/T]ACAAAAATGTAAAAG | 9474 |
rs149804919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311802 | ACTAAAAGCAGGAAA[C/G]TGGTTACTACTGTGC | 9474 |
rs149809037 | snp | C/T | 0.00119784 | 0.0244435 | intron-variant | ATG5 | GRCh38.p7 | 6:106205332 | CAAAGTCAAAGGAAT[C/T]TTTTCAAGAATTTGG | 9474 |
rs149814761 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106267921 | ATACCATTCAGGACA[C/T]AGGCATGGGAAAAGA | 9474 |
rs149816715 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106190506 | TGCACATATTGCATT[G/T]AATTTTTATGTCTCT | 9474 |
rs149826841 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258341 | CCTTACCACTGCATC[-/T]TAGCCTGGGTGACAG | 9474 |
rs149833563 | in-del | -/CTTT | 0.0471551 | 0.14613 | intron-variant | ATG5 | GRCh38.p7 | 6:106306809 | CTCTGTTTACACTTC[-/CTTT]AAGTCGCCTTCCCAT | 9474 |
rs149904617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223548 | TACCTATTTCTTTTA[A/T]AAGGTGTGTAAGTAG | 9474 |
rs149931593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216370 | CTATCAATTGGTGAA[C/T]TGATAAACAAAATGT | 9474 |
rs149966646 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261923 | GGACAGCCCCAACCC[C/T]CACAGCCACATCAAA | 9474 |
rs149984905 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ATG5 | GRCh38.p7 | 6:106209751 | TGTACTGTAATTATG[A/C]AAGATGTTAGAATTG | 9474 |
rs150026209 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106231881 | GGCCCTCAGGCAAGC[A/G]GACTTTGGAGGCACT | 9474 |
rs150083805 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293085 | TGCAAGAAGATCAAA[C/T]AGCAAACCAATTGGA | 9474 |
rs150110364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106286114 | TATGCATGTGCAACC[C/T]AGGCCTCAGCCAAGC | 9474 |
rs150120386 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ATG5 | GRCh38.p7 | 6:106245814 | GAAATGAAAGGTGTT[A/C]ATCAAAATGCTGCAC | 9474 |
rs150128298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233302 | AGGTTTCTGCCAAAT[A/G]TGGATTCCCAGGTAC | 9474 |
rs150173989 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106239990 | ACAACACATTGTGGG[A/T]AAGGACCTTCTTTTT | 9474 |
rs150184055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197333 | TAAGACCAGCCTGGG[C/T]AACACAGTGAGACCC | 9474 |
rs150205905 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302601 | AAGGCATACTTAGAA[A/G]CCAGAATCACAATCT | 9474 |
rs150321257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106251139 | TGCTTGCTCTGGAGG[C/T]CTGCATGGGCTGCCC | 9474 |
rs150326257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313798 | TATATTGGCACTAAA[A/C]TCCTCATCTGTAATT | 9474 |
rs150331377 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106207848 | CCTGTAATTCCAGCA[A/C]TTTGGGAGGCCGAGG | 9474 |
rs150384992 | snp | C/T | 0.115438 | 0.210697 | intron-variant | ATG5 | GRCh38.p7 | 6:106202722 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 9474 |
rs150389752 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106265387 | GAAGAGACTTGAACT[C/T]CCACACAATAATAGT | 9474 |
rs150400040 | in-del | -/AG | 0.1652 | 0.235179 | intron-variant | ATG5 | GRCh38.p7 | 6:106229570 | ATAGTAAAAAAAAAC[-/AG]TGTGCCCTATTCCTT | 9474 |
rs150426288 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106225097 | TGCAATTTAATTTAT[C/T]ATGTGCCAGGCACAA | 9474 |
rs150479393 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106291489 | ATGGAAACAGATTTG[A/G]CCTGATGAATCCATT | 9474 |
rs150480917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220184 | ATACCATAAGCAATC[G/T]GCAAAAGAAGCAACT | 9474 |
rs150521483 | in-del | -/AAAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318775 | AAAATACACAGACCC[-/AAAT]TTATAGGATCTTAAA | 9474 |
rs150531155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226527 | TTATTTTAAATATGC[A/G]CAAAGAACTAAAAAA | 9474 |
rs150581590 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106293375 | TTTATCAGCCATGTG[A/T]ACTGTTATGTCACAG | 9474 |
rs150584806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221996 | TTCCAGGTTCAAGCA[A/G]TCCTTGTGCCTCAGC | 9474 |
rs150634912 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106288073 | CCCCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9474 |
rs150694586 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106320001 | ACTCCAGAAACACTA[C/T]ACATTTTACATTACC | 9474 |
rs150707065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106200187 | ATTTTGGGCTCCATA[C/T]TCTTTGCTTAGTCAT | 9474 |
rs150729039 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106304759 | AGTAGCTACACAACT[A/G]TACACAATTGTTTGA | 9474 |
rs150739119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262446 | TGATCTACAGAAAGG[G/T]GGTAAGAAGCTAACA | 9474 |
rs150760629 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106194309 | TGACAAATGTGATTA[G/T]TGCTCAAATATTATC | 9474 |
rs150792914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257320 | GTAAATAGTAACATA[A/G]TCGTTTATCATTATC | 9474 |
rs150851322 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ATG5 | GRCh38.p7 | 6:106315867 | CATACATGTAAGGAA[A/C]ACAAAGTCCAGAACG | 9474 |
rs150856339 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106209368 | AGGAACAAACTACTG[A/G]TATATGCAACAACTT | 9474 |
rs150908955 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106278651 | TTTCTATTCAAATTT[A/C]ATTCCCAACATTATC | 9474 |
rs150942820 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231583 | ATAACACAGGGAAAG[A/G]AAGAAAATCCTACCG | 9474 |
rs150957952 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106285778 | CACTAAATCTGTATT[A/T]CATGCAATTTTCACG | 9474 |
rs150960253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106211893 | AGCTACTTTGTGTGT[A/G]TGCTTTGTTTTTAAG | 9474 |
rs151011413 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106281254 | GAAATCAAGAGTACA[A/G]TTAAATGAGTTTTGA | 9474 |
rs151044927 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106268540 | AGTATATTCCCAAAG[C/G]ATTATAAATCATTCT | 9474 |
rs151099472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310594 | AAAATTTACCATTTA[A/C]ACCATTTTTAAGTGT | 9474 |
rs151106788 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106298027 | TGGAATGCAGTTGTG[C/T]GATCTTGGCTCACTA | 9474 |
rs151109107 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106224456 | AGTATTGACCTGGTA[A/T]CTTGAAGAAAAGTAA | 9474 |
rs151111639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106189208 | ATTAAAACAACAAAG[C/T]AAAAAATGTTTCCAG | 9474 |
rs151136970 | in-del | -/ATTAGTT | 0.0644693 | 0.167566 | intron-variant | ATG5 | GRCh38.p7 | 6:106250264 | GTATATTTTTAAAAA[-/ATTAGTT]ATTTCTTCTTACACC | 9474 |
rs151160490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106289389 | CCTAAATGAATGGAA[C/T]TTAGTATATACAGAA | 9474 |
rs151165328 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184121 | CATAACTCAAATATT[A/G]CTATTTTTTTCTGCC | 9474 |
rs151170923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250650 | ATGTGACAGCTAAAT[A/G]TAATGATTCTTCATG | 9474 |
rs151177169 | in-del | -/CTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307535 | TTTGATTTCAATACC[-/CTTT]TTTTTTTTTTTTTTT | 9474 |
rs151183529 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214389 | GAGAAATAGGAGAGT[-/T]GAAAATAAGCACTTT | 9474 |
rs151224461 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106244944 | AAGGAATTCACAGTC[A/G]TTTTACAAATCTTTT | 9474 |
rs151247406 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322299 | GTTTCTTTCACACTA[C/T]ATACCAAGAAAAACT | 9474 |
rs151256220 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106306892 | CCTTATCTATGCTGC[G/T]TGAGGTCTAGAACTA | 9474 |
rs151260089 | snp | C/T | 0.000181505 | 0.00952467 | intron-variant | ATG5 | GRCh38.p7 | 6:106201954 | AAAGAAATGTTTTAA[C/T]GTTGCTGATTGTATT | 9474 |
rs151290510 | in-del | -/TG | 0.196149 | 0.244131 | intron-variant | ATG5 | GRCh38.p7 | 6:106290058 | GACAGAGTTTCACTC[-/TG]TCACCCAGGATAGAG | 9474 |
rs151318474 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106260919 | AGGGGTCAGGTGTGG[A/G]GGCTTGACATTCTCA | 9474 |
rs151327942 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106218811 | AATTACCTTTGGCAT[A/G]ATGAAAAAAACTTTA | 9474 |
rs180674564 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106250770 | TGGATAGAACACTAT[G/T]AACATAATTTCTCAT | 9474 |
rs180678810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106271057 | ATTGAACAGCTCTTA[C/T]ATCATATTCTACATC | 9474 |
rs180692492 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106292571 | TTGTCCCCTCTGTAC[A/T]TCCATATCCACATCT | 9474 |
rs180697033 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106212531 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 9474 |
rs180701830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106192797 | TAAAAAATAGAGCGA[C/T]GAGCTTTCTGATTAC | 9474 |
rs180711356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232828 | AGAGGAAGCAGAGTG[A/G]TTTACAGACCTGGAC | 9474 |
rs180824718 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327593 | ACAGTCCCAGCTACT[C/G]CAGTGGTTGAGGAAG | 9474 |
rs180834394 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106322942 | TATTTTATTTTGAGA[C/T]GGGGTCTCGCTCTGT | 9474 |
rs180860715 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106262972 | TCGTACTTCAGTGGC[A/G]CCTGGAACCCCAGAG | 9474 |
rs180869468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284056 | GGATACATACAGTAT[A/T]TTGTTTATTCATCAG | 9474 |
rs180873184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312034 | ATGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT | 9474 |
rs180876696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106300831 | CAAGAGTATGTATTT[C/T]TTTTTACAATTCAAA | 9474 |
rs180883723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306825 | TTTAAGTCGCCTTCC[C/T]ATTCCAAAATCTCCA | 9474 |
rs180886120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296558 | CGTGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 9474 |
rs180896836 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316191 | CACATCTCGAAGCAC[A/G]TCTTTGTCATCTGTC | 9474 |
rs180911716 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106324941 | GTCTCCGGGTTCTGA[C/T]TGCTCAAGACAGGCT | 9474 |
rs180918559 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208739 | AATGAAAACATAAGC[C/G/T]GCAGGCTGGGAGAAA | 9474 |
rs180921614 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267199 | TCCTATACACCAACA[C/G]CAAAGAAGCAGAGAG | 9474 |
rs180922110 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106235596 | ACTTAGCTCACACCC[A/G]ACCAATCAGGTAGTA | 9474 |
rs180922424 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106257292 | AGGTGAACACTCTAA[A/C]ATAATGAAAAAAGTA | 9474 |
rs180973485 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ATG5 | GRCh38.p7 | 6:106289531 | ATTTCCTTATTAACT[A/G]TAAGATTCTTTTTTC | 9474 |
rs180995113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247779 | TTGTTTATAGTATGA[C/G]AGCTGAGACAAGAAG | 9474 |
rs181191854 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198648 | CAGGCATGGTGGCAG[C/G]CACCTGTAATCCCAG | 9474 |
rs181225068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216274 | GAGAAATGAAAATAT[A/C]TGTTCACCAAAACAT | 9474 |
rs181281595 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106312710 | ACTGAGCACTGCAGG[A/G]CTAACAGGACAATGC | 9474 |
rs181307927 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106251546 | AAAAATCTGTATTAA[C/T]TGATATTAACTTTAA | 9474 |
rs181308122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271482 | AGGGCCCTCATCAGA[C/T]ACTGAATTGCAGGCA | 9474 |
rs181315528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292889 | AAGTATCTTATAGAC[A/T]AATACTAATCGAAGC | 9474 |
rs181328529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233041 | CACTCTTGTCCTTTG[C/G]TATGTGGATGATTTT | 9474 |
rs181330220 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213295 | GCACTATGAAAAAAA[G/T]TACAAAGCTTGAGCA | 9474 |
rs181402317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281870 | TTTTAGTCATTCTAG[C/T]GAGTGTAATGTAATG | 9474 |
rs181419053 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106319767 | CGTTAGGGAGAAGGA[A/T]CATATCTCATTCATC | 9474 |
rs181432200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106241483 | TATGATAGGAATATG[C/T]ATTTCTGGGTAAATA | 9474 |
rs181442543 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106287052 | TTGTCAGACAATAGT[A/T]GATAACTAATACAAC | 9474 |
rs181448687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306014 | CATATAGCTACAATG[A/G]GCTTACAGCATGACA | 9474 |
rs181458752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106228554 | AGGCCAAGAACCCCA[A/G]GTCAGAGAACACGAG | 9474 |
rs181463451 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106203258 | AATTGTTTCATTTAC[A/T]AAATTTCCTTAGTGA | 9474 |
rs181472502 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106246978 | CGCCTTCATGAAAAA[A/T]ATGGACTATTTGAAA | 9474 |
rs181478595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265984 | TAGCACAAGACAAGA[A/T]TAATTAAGATCAGAG | 9474 |
rs181482536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106257535 | AGTCCACTGTTGACT[C/G]AAACATCATAATGCA | 9474 |
rs181497788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106207606 | AAATGTAGCCAGTAG[A/G]GCCAATAGGTTAACC | 9474 |
rs181501360 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184635 | AAGCTATGATGCTGG[C/T]ACAATAATGAATGAG | 9474 |
rs181503164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216710 | GACTCCTAAAACCAA[C/T]GAATAGCATGCTTTA | 9474 |
rs181529026 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106299790 | GCAAACTAATACAAG[C/T]ATTCTAAAATCAGCA | 9474 |
rs181564729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193791 | CTTTATTTAAAATAT[A/G]GACAATAATTGTACT | 9474 |
rs181568732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261802 | GGCTGGATGTAGAAG[C/T]TGGGTTGAAAAAAAT | 9474 |
rs181597003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222151 | GTGCTAGGATTACAT[A/G]CGTGAGCCACTGCGT | 9474 |
rs181612439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236666 | CTTAAATTTGTAACT[A/G]AAGGTGCTTTCCTGA | 9474 |
rs181619101 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106278533 | TTCACCTTTACTGCA[C/T]ATAAGTTCCTCAGTA | 9474 |
rs181639201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283606 | ACTTAGTGTGGAAAT[A/T]CAATCGGCATAGCAC | 9474 |
rs181640991 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106199031 | AGCCATTAGAAAAAT[G/T]AGAATTAAAATCATC | 9474 |
rs181668128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223324 | TAGAAAATAGAAATG[G/T]AATTTTAAACTATTC | 9474 |
rs181674920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242620 | GAAAAATACTATAAA[C/T]AACAACAACAAAAAA | 9474 |
rs181678203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106262491 | GGATTAGAAAAGTAA[A/G]TACATCTAAAGTTTT | 9474 |
rs181704894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323718 | AATGGCCTACTAACA[A/G]CTCTTATTTCTGCAC | 9474 |
rs181710364 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106297383 | CTCAGTCTAATTGGT[A/G]TTGATTCACATAAAA | 9474 |
rs181789982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106299985 | TGATTGCTGTGAATA[C/T]TGACTTACTCTATAT | 9474 |
rs181799106 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269794 | CGCCTCTCCCTCCAC[A/C]CCTCCCTGCATGCTG | 9474 |
rs181857085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203841 | CACTTAGGCATTAGC[A/G]ACAAGGTTTTGTTTT | 9474 |
rs181872038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316541 | CAGTCAAAATGAAAC[C/T]GTATCTGCATCAGTC | 9474 |
rs182016279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232227 | GGTGTGGCCTTCTCA[A/G]TCTTATTTTCCTGTC | 9474 |
rs182023919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215470 | AATTTATTCTACTAA[A/G]GTAACATCAAAGGGA | 9474 |
rs182030984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197156 | AGTCAAGGATGTTAT[A/T]AAAAAGGAAGTTTAA | 9474 |
rs182033570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288623 | TCTCTAACTCTTGTT[A/G]ATCAACATGTGGTCT | 9474 |
rs182036740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324555 | GTTTACTATTTTGTT[C/T]ACTGTTTTGTCCAGT | 9474 |
rs182038556 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106306650 | TCACACAAAATTCTG[A/C]GATAATCTGTAATAC | 9474 |
rs182040012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106191698 | AGTGACTCTTCTCCA[C/T]CCCTCTCTCCTGCTC | 9474 |
rs182052961 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ATG5 | GRCh38.p7 | 6:106320909 | GCCAGGTAGTAATTT[A/C]AGCAACTAAGGCAAA | 9474 |
rs182106065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106214062 | CAGGGGTTTACACAG[A/G]ATATGCTGCCAGACT | 9474 |
rs182111400 | snp | A/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106194489 | CATAATCTAATCATA[A/T]ACAGCAAAGGAGAAA | 9474 |
rs182237624 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316705 | CTCCAGATAGTTTCT[C/G]CTCTCTTCCTGCAAA | 9474 |
rs182277871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106234013 | TCTTTGCATGCATGC[A/G]AATACTCATTATTGG | 9474 |
rs182287926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252751 | AGCTGGCTAGGACCC[C/T]CATGCAGGAAACCGA | 9474 |
rs182293361 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106211698 | CTGGGCAACAGAGTG[A/G]GACTGCTCAGGATCT | 9474 |
rs182293598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106207889 | ACGAGGTCGGGAGTC[C/T]GAGACCAGCCTGGCC | 9474 |
rs182298129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317661 | AACAACTACTTTAAG[C/T]GAATGATATACATGC | 9474 |
rs182303744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249751 | TGGATTCCAATTAGT[A/C]CACATCCTTGCCAAT | 9474 |
rs182313533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247135 | AAATAACTATAGAAG[G/T]AACTATTGGTAAAGA | 9474 |
rs182331152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106279013 | CCTGGTGTTACTTAA[C/T]TAAACCATGATAACT | 9474 |
rs182336151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297875 | CAGGAGTTCGACACT[A/T]GCCTGAGCAACATGG | 9474 |
rs182346042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106223531 | CCCTACAGGACTCAA[C/T]TTACCTATTTCTTTT | 9474 |
rs182355404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259376 | TAACAGTAAAAATAA[G/T]AATAAAGTTATTAAA | 9474 |
rs182456057 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185877 | AGTGATCTACTGTAT[A/G]TGAGTCAGAAAGTAC | 9474 |
rs182512428 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106266816 | TCCCTTCATGCTAAA[A/C]ACTCTCAATAAGCTA | 9474 |
rs182533045 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106294125 | CTTAGATTCTGGATT[C/T]CAAATTGTGGGATTT | 9474 |
rs182554406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229132 | TACTTCCTCTGATCC[C/T]TGCCTCCTAGGTACT | 9474 |
rs182564463 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106275274 | AAAATATATTTTCTA[C/G]AAGCAACATTTACCA | 9474 |
rs182574329 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294736 | CAGCCCTAGCTACTC[A/G]GGAGGCTGAGGCGGG | 9474 |
rs182580577 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314359 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT | 9474 |
rs182588565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309511 | ACAAGCTGCTGAATA[A/G]TATTATGCATTCAAC | 9474 |
rs182594285 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185185 | TAATCAGTGAAAATC[A/G]CAAAAGGAAAAAGAA | 9474 |
rs182612378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204249 | GAAAAAATAAATAAA[A/G]ATAAGTAGAAAAAAT | 9474 |
rs182617610 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243472 | GGCAGAGGCTGTAGT[A/G]AGCTGAGATCACATC | 9474 |
rs182636148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239235 | TAAATAACTAGAAAT[A/G]GAAACAAAATAAAGA | 9474 |
rs182650157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204780 | CCCACAAGCCATACG[G/T]AACTGTGAGTCAATT | 9474 |
rs182662605 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200354 | ATTCAGAATACATTC[A/G]TAAGAAACAAGCATT | 9474 |
rs182684491 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188975 | TTAGAATAGGGCAGC[A/C]GAAACTTCAAACCGA | 9474 |
rs182723173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229865 | GTGAGCACACCTCAC[C/T]GGTTCAGAATTATTC | 9474 |
rs182784404 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106234968 | GCTGTTTATTTTTAG[C/G]GGAAGAATGTTGTTA | 9474 |
rs182787274 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106273037 | CTTATTTATACAATG[C/T]AATCTCAGTGTTCCA | 9474 |
rs182788407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106253602 | CAATTACTTCTCTCC[A/G]TGTTCACCACTACCA | 9474 |
rs182812461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313620 | CAATATTCTCTGAAA[A/C]ATAAAACATAATGCT | 9474 |
rs182847425 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106308179 | CCAGTCATCCATGCA[A/T]CCAAACAGAAGGCAG | 9474 |
rs182850487 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106323005 | GCTCTCTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 9474 |
rs182866260 | snp | A/G | 0.00386905 | 0.0438127 | intron-variant | ATG5 | GRCh38.p7 | 6:106248107 | TCAATTAAGATGTCT[A/G]AGGCTTTCATAAATG | 9474 |
rs182871883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201815 | TAATTTACAAAATAA[A/T]ATATTAAATATTAGG | 9474 |
rs182875258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106325137 | TCGTAAATAGATAAA[C/T]TGCTTGGAGGACATA | 9474 |
rs182877945 | snp | G/T | 0.0217236 | 0.101931 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326543 | GATAGGGCCACCGCA[G/T]TCCCGCCTGGGCGAA | 9474 |
rs182879720 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267439 | TACAGATTCAACGCT[A/T]TTCCCATCAAGCTAC | 9474 |
rs182886401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106290139 | TCAAGTGATCCTTCC[A/G]CTTCAGCTTCCCAAG | 9474 |
rs182890434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303068 | AGAAACTAGAAAAAA[A/T]TAATAAAACCAAAGG | 9474 |
rs182895236 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106323032 | TCATGCCATTCTCCT[C/G]CTTCAGCCTCCCAGT | 9474 |
rs182900201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218711 | AATACATAAGCAGAC[A/G]TCAGAATTGTCCCAA | 9474 |
rs182909529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106244378 | ATACAGAGAAAACTC[A/G]TTAATATGGCCTGAC | 9474 |
rs182912758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264094 | GGAAGCTAAGAATCT[C/T]GATAAAAGGTTATAG | 9474 |
rs182923882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284821 | TTACAGAAATGTCTA[C/T]TCGAATCCTTTGACT | 9474 |
rs182932052 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205486 | ATCATTACACATTGC[A/C]TGCTTATAGCAAAAG | 9474 |
rs182948389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224492 | GAGGAAACTGGACAC[G/T]GAAACAGAAGAAGTA | 9474 |
rs183107277 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325757 | GAATACAACCGGCAA[C/T]GCTGCGGAGCCCTGG | 9474 |
rs183119351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106284508 | GCACATGCCACCACA[C/T]CAGGCTATTTTTTAA | 9474 |
rs183141983 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106308659 | AAGGTTAAAGGTTAA[C/G]ATGTTTTAATATTTC | 9474 |
rs183149523 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106244075 | GCTTACCACCCCATC[C/T]GGCTCATTTAAAAAA | 9474 |
rs183235466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188368 | CTTCCTCCTACTTAG[C/T]ACTGAGTCAAAAAAT | 9474 |
rs183371014 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106263466 | GAAGAGAGGAGCTGA[G/T]CCTGACAAGACGGAT | 9474 |
rs183379240 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259636 | CTCCTTTCTTACATT[A/C]TAGGTAGACAAATAT | 9474 |
rs183403837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298044 | ATCTTGGCTCACTAC[A/C]ACCTCTGCCTCCCAG | 9474 |
rs183413636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223931 | GGAGGTTAAATTAGT[G/T]AATTCTTCCAGCCTC | 9474 |
rs183415736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106219413 | TAACACAGTCAGCCC[C/T]CCCTATCCAGGGGTT | 9474 |
rs183477120 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106313407 | CATAAACGGATCGCT[A/G]CCTAATGTTAAGGGT | 9474 |
rs183494482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233393 | TTAGTAAGATGGACA[A/C]CTGAAGCAGAAGCGG | 9474 |
rs183498552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278771 | CTGGAGACAAGGAGG[C/T]AACACGACTATGTGC | 9474 |
rs183515573 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106238451 | GGATGGGATTCTGGG[A/G]GCTAACCCATCCCTC | 9474 |
rs183517994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272395 | GCCCTGAACAGGCAG[C/T]GTCTCTGCCTGACTT | 9474 |
rs183518881 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106217523 | GCTCGCCACCAGTTA[C/G]GGTAGCCAAGAACTC | 9474 |
rs183519593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194050 | TCTTCTGTCAGTCCA[C/G]TAATGTCATCATTTC | 9474 |
rs183529587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258053 | GAAGCCAAATTGACA[C/T]AAGTTATCACAATTT | 9474 |
rs183548252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199414 | ACACTTGCTTCAATA[C/T]GGATGCAACTCAAAT | 9474 |
rs183575189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106304289 | GTAAAATTTTTTTAA[A/G]TTATAAAAATAAAAA | 9474 |
rs183576792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257116 | TACAAAGTGGGAGGA[C/T]CATCAATATCACTGT | 9474 |
rs183580269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323350 | CATGGGTCACTGTAA[C/T]CTTGAGCTCAAGGGG | 9474 |
rs183580614 | snp | A/C/G/T | 0.00159649 | 0.0282165 | intron-variant | ATG5 | GRCh38.p7 | 6:106276774 | CTTTACACGATCCTC[A/C/G/T]TCTTTTTCTATTTAG | 9474 |
rs183583112 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295958 | TCAATATTTAAAAAA[C/T]GAGAAAACTATAAAT | 9474 |
rs183591995 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106197338 | CCAGCCTGGGCAACA[C/G]AGTGAGACCCTGCCT | 9474 |
rs183592887 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317843 | CTTGCTCTTTTTAAA[C/G]TGAATTCACTAGTGG | 9474 |
rs183599828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106215489 | ACATCAAAGGGAAAT[C/T]TCATAAAAATTCTTT | 9474 |
rs183599946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285768 | TTATGGTCATCACTA[A/T]ATCTGTATTTCATGC | 9474 |
rs183632915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280456 | TTCACTTTGACTAGG[A/T]TAAGCTTACTATAAG | 9474 |
rs183636621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281532 | TTTTGTTGCTGAGTA[C/G]CAGGCCATTTAATGA | 9474 |
rs183677750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106240295 | TGCAATGTGTTTGAC[A/G]GTAAAAGTTTAATAT | 9474 |
rs183686979 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315928 | TCCTCTGAGTGGTAG[C/G]ATTAGAGGTGATTAT | 9474 |
rs183707001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293631 | ATTAGGACTATCCTT[C/T]ACAAACTGTACTATA | 9474 |
rs183718578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106290376 | CCCAGGATGAAGTGC[A/G]GTTGTCTGATCATGG | 9474 |
rs183731646 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106252048 | ATTTCACCATGTTGG[A/C]CAGGCTGGTCTTGGA | 9474 |
rs183760463 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106213726 | CTCCCAACAACGTAC[A/T]GTGTATCTAGAGCAA | 9474 |
rs183794699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319505 | CTACTAAACATACTA[C/T]GCACTTTCTGTCCTT | 9474 |
rs183830199 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106230998 | TCCCTACCCCAGCAT[C/G]CCCCAGACTCCTTCC | 9474 |
rs183832107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249168 | TCACCCCTTTTAAAG[C/T]ATACAACTTAGTGGT | 9474 |
rs183857072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211290 | CAGTAGATGCACAAT[A/G]CACTGGGTTGTAAAA | 9474 |
rs183861829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190260 | AAGATCAAAGTGCTG[A/G]CACCTGGTATGAGCT | 9474 |
rs184002405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106248404 | TTTCCATAAACATAA[A/G]GCAAATATAAAATTA | 9474 |
rs184048818 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106210641 | CTCTGGATGGCACTT[G/T]ATGACGATGGATTCA | 9474 |
rs184049952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226910 | AGATAGGTCAATTGC[A/G]AGAAAGAGAGGGAAG | 9474 |
rs184159509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230278 | GACTCAAAAGCTTAC[G/T]TATACCCTCTCTGAA | 9474 |
rs184161041 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106297637 | TTTGCTGTACTTAAA[A/C]CTGTATTAAAATTTC | 9474 |
rs184164783 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106267641 | TGGTACCAAAACAGA[G/T]ATATAGACCAATGGA | 9474 |
rs184268220 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184385 | CCCTCCATCCTATTT[C/T]TCCAAGAAACTTTTA | 9474 |
rs184277614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207037 | ACCTGATCTTGCCAC[A/G]TATTTGTAAATATGC | 9474 |
rs184314758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106264920 | GACCAACACTATGAA[A/G]AAACTGCATCAACTA | 9474 |
rs184341419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224984 | TAAAACAAAAGAATA[C/T]AGGAGGCATGACAAG | 9474 |
rs184350122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241065 | GGCTGAGGCAGGAGA[A/C]TCACTTGAGCCTGGG | 9474 |
rs184363036 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106315815 | GAAAAAGAAAGTCAA[A/G]AAGGCACCATAGCTG | 9474 |
rs184378331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203108 | GGGTGTATGATTTTA[A/G]TAGTTTCATTATTTC | 9474 |
rs184391849 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106268143 | TACCTATCAGACAAA[A/G]GTCTAATATCTAGAA | 9474 |
rs184433094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106244482 | TTTGCCTACAAAGCT[C/T]TTCTCATGACTCTTT | 9474 |
rs184465888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269226 | ACAAACCCTGAGCTA[C/G]ACACAGGGTGCTGAT | 9474 |
rs184470812 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291470 | ATCCTGATATTATTA[C/T]ATCATGGAAACAGAT | 9474 |
rs184471627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205708 | TTCACCCTTTCCCAA[A/T]TCTGAGCAAGTATTA | 9474 |
rs184482057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327183 | TTCCCAGTGTCAGAC[A/G]AAAGTATATAAAATT | 9474 |
rs184483162 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106309951 | AAACACCACAGCTAA[C/T]GGGTATGGATATATC | 9474 |
rs184486265 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106290932 | AAATTTTCACTAAAA[A/T]GTTGAAATTTTACCA | 9474 |
rs184489785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231749 | GTCTGCCTTAGGCCC[A/G]GAACAAAACTTAGAA | 9474 |
rs184492686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261128 | GGGAAAGAAGAGTTG[C/T]TAAAATATGCAGAGA | 9474 |
rs184509744 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106249265 | CACTTCCCACTCCCC[A/C]TTGCCCCAGCCCCTG | 9474 |
rs184516435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221245 | CAGGCAGTAGACTTA[A/C]ATTTTGTAATATTTT | 9474 |
rs184536273 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106229113 | TTCTCCTTACCTCTG[A/T]ATCTACTTCCTCTGA | 9474 |
rs184548938 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106246980 | CCTTCATGAAAAATA[A/C/T]GGACTATTTGAAAAT | 9474 |
rs184565071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298421 | CTGGGCGTGGTGGCA[C/T]GCACCTGTAGTCCCA | 9474 |
rs184597205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106260223 | GTAACAAACCTGCAC[A/G]TTGTGCACATGTACC | 9474 |
rs184599776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280946 | ATTATTTTACAAAGT[C/T]ATTATCCTATATGTC | 9474 |
rs184601159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286823 | CAAGAAGATAGGCCC[C/T]TCAATCCTACAACCA | 9474 |
rs184620698 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106323506 | GGATTCTCTCAAAGA[C/T]GGTATTACAAGCATG | 9474 |
rs184630176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245639 | CTGTCTCTCTCTCTC[C/T]GGTTATGCAGAAATT | 9474 |
rs184681995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323873 | CTAAATGACTTGGCC[A/C]CATTTCCACCTAAGT | 9474 |
rs184706750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265995 | AAGAATAATTAAGAT[A/C]AGAGCAGAATTGAAG | 9474 |
rs184708785 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106287789 | ACAAAGAGAGAAAAA[A/T]TTTTTTTAATTTTAA | 9474 |
rs184718252 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306500 | TGGCACTTGTAGGAA[C/G]AGGCCAGAGCTGCTG | 9474 |
rs184737134 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327291 | TAAAATATAATGGTA[A/G]AATATAATGGTAAAA | 9474 |
rs184746873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304720 | ATTTTGTGAAATTAA[A/G]TATCTTATTATCTTG | 9474 |
rs184792372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106202669 | AACTTAATCTTCTTT[C/T]TCTTTTTTTGGAGAC | 9474 |
rs184794009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106265759 | CTACTTGGTAAATAA[C/T]GAAATTAAGGCAGAA | 9474 |
rs184806690 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106240671 | GTAAGCTGGCAATTT[G/T]TTTTTTAATCTCTAC | 9474 |
rs184809705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220795 | AAGGTAGTTTTCACT[A/G]TGGAAATAGGTAAGT | 9474 |
rs185022861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195055 | CTTGACTAATTCCCT[A/T]AGCCATTTACAAAAA | 9474 |
rs185082437 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106213101 | ATCTTAATAGTAGTA[C/G]CCAAGTGCAGGATCT | 9474 |
rs185082955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106299876 | TAAATGCCTCCTATT[C/T]GGAAAGTTGCTGCAT | 9474 |
rs185090052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192820 | CTGATTACCACTAGC[C/T]TGAACAATTTTGTTC | 9474 |
rs185091957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232866 | ATGCCTTTTTCTGCA[C/T]CCCTGTACATCCTGA | 9474 |
rs185166547 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106191129 | TGTGGGAAATTAAAA[G/T]AATATATACATATAT | 9474 |
rs185177944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276119 | TAGTGTTTCATAAGG[C/T]CTCTACAGATATCAA | 9474 |
rs185189607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282960 | CTCAGCTAATTTTTT[A/T]AATTTTTTTTTGTAG | 9474 |
rs185204415 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106320298 | GAGGAGGGGTTGGAG[A/G]TATTAATACATCCTA | 9474 |
rs185204968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196811 | CCCAACTAATTTCTT[C/T]CCACTCTAGGCACTC | 9474 |
rs185219894 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106235304 | ATGACTAAGATCTAC[C/T]GTGGACCCCTGGACC | 9474 |
rs185220405 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238459 | TTCTGGGAGCTAACC[C/T]ATCCCTCTCTCCCCT | 9474 |
rs185226295 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217924 | TCAAGTCAAATTATA[A/T]GCTTATTTTCCACAA | 9474 |
rs185237227 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106258209 | TCCCGTCTCTAACAA[A/C]AAAAAAAAATTAGCC | 9474 |
rs185241026 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106211595 | TGCATCTGTAGTCCC[A/G]GCTACTCAGGAGGCT | 9474 |
rs185246755 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106250919 | TACTGCAACAACTAT[C/G]TTAAGATTTCTCAGC | 9474 |
rs185253679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199918 | ACTATAAAGGCTAGT[A/C]AAGTTCAAGGAAGAC | 9474 |
rs185261043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271175 | TTCTCATCTCTCCAA[A/G]CTCATCTCGGGCCAC | 9474 |
rs185291589 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106255542 | CTGTAAGTTACAACA[A/T]CTTTAAACGTATTCC | 9474 |
rs185300253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106296678 | CAAAAATTAGCTGGG[C/T]GTGGTCGCATGTGTC | 9474 |
rs185300342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247833 | TCTGCTGGGAAATGA[A/G]CATCAGGTGAATCAA | 9474 |
rs185300628 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267224 | AGAGAGTCAAATCAT[A/G]AGTGAACTCCCATTC | 9474 |
rs185306016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316336 | CTAGAAAACAAAAGA[C/T]TATTTTAAAAAATCC | 9474 |
rs185306494 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295416 | TAATCTATTAGATAA[C/G]ATTCACTCGAGATCA | 9474 |
rs185310810 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106214941 | GTAAATTCTCTAAAA[A/T]TTTCTCCCAAAAGAT | 9474 |
rs185320825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209021 | CAAAATAAAAATTAG[A/T]GGTAACACCAAATGC | 9474 |
rs185325269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106257408 | TATGACAGTATCACC[A/G]CAAATCTATGAGTAA | 9474 |
rs185329702 | snp | A/G | 0.000304296 | 0.0123311 | intron-variant | ATG5 | GRCh38.p7 | 6:106186704 | AGAAACCCAACAACA[A/G]TAAAAGTCAAAACAG | 9474 |
rs185342759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106277996 | GTCACTCAGAGTGGA[A/G]TGTGGTGGCACAATC | 9474 |
rs185342820 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106229598 | CCTTTAAAAGCCAGG[A/G]TAAATGTAAAACCTA | 9474 |
rs185344396 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106315380 | CCTATTATGGGCTAT[A/T]CAGTGAACAGGCAGG | 9474 |
rs185419420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318227 | ATTCCAGGACACCAC[C/T]TGACATGTTTATTAA | 9474 |
rs185423886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292230 | TCAACTAATATAAGA[C/G]ACCGACATGGTGGAA | 9474 |
rs185433799 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106212071 | AAAGTTCATTTATTG[A/G]TTAATCAAGAATATA | 9474 |
rs185439566 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ATG5 | GRCh38.p7 | 6:106322944 | TTTTATTTTGAGACG[A/G]GGTCTCGCTCTGTCG | 9474 |
rs185450805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250399 | TTCTGAATCCAGTAA[G/T]TCCAGCACAATTTCA | 9474 |
rs185478958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300946 | CAGTTGACAAAATGA[A/G]AAGCTTGTTCTAAAT | 9474 |
rs185515481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311508 | CTTTTCCAAACAGGG[C/G]ACACTGCAAGACAAA | 9474 |
rs185547886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269893 | TCAAGTGCCCCCAAA[A/G]TAGGAGCCCAGGCAG | 9474 |
rs185548825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293167 | ATAACTACAAGGCCA[A/C]AATAAATTTCCAACA | 9474 |
rs185557160 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106313050 | GGAGCCAGCAGATAA[C/G]AAGTTGAAAGTAAAA | 9474 |
rs185582305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106232281 | GTCACTATCCAAGGG[A/G]TCCTAGGACAGCCAG | 9474 |
rs185780171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251576 | ATCTTCTTATAGAAA[C/T]GCTATATTCTTATAT | 9474 |
rs185784182 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271790 | TACACAGAATGCTTT[A/T]AAAAAAAAAATGGTG | 9474 |
rs185798957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191994 | TCCATTTTTATGCAG[C/T]ATGGCATATAATTTT | 9474 |
rs185857928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266936 | ATTCCCTTTGAAAAC[A/G]GCCACAAGACAAGGA | 9474 |
rs185875957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106306682 | TATAATGCAATACAA[C/T]GTAAATAACTATAGC | 9474 |
rs185898982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229279 | TCCCTCCTGATTTAG[A/G]TATACAGCTCTAGAC | 9474 |
rs185922930 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185758 | ACACAGGTTTTTTAA[C/T]TGGCAGCAAGAAATT | 9474 |
rs185971542 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325620 | GGGGCAAGCTGCCCG[C/T]CTGACACACTGTCCT | 9474 |
rs185997542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288945 | CCAAATGTGTGTGTG[C/T]GTGTGGCAGAGGCAA | 9474 |
rs186020733 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106208558 | TTTCTATATGGCAAG[A/G]AAAAAAAAAAGGGCA | 9474 |
rs186026887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222195 | TCTTATTATAACCAA[C/G]AATTTATTTGTGGAG | 9474 |
rs186031416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247715 | AAATCACTAATAAAA[A/T]GCACAAAAATGTAAA | 9474 |
rs186069327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203579 | ATTAAAACTTAACAA[A/G]AACAGAGAAATGCCA | 9474 |
rs186108979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312353 | GAGGACCAGATTTTT[C/T]TGGGGGGAAAGCTGA | 9474 |
rs186112726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199362 | CAAAATGTGATGTAT[C/T]TACCCAATGGAGTAT | 9474 |
rs186113070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284079 | TTCATCAGCTGATGG[A/G]CATTGGGTTATTTCC | 9474 |
rs186134965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207636 | CAATATTAACATTAA[C/T]GTTGATAAAACAAGA | 9474 |
rs186135938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106204547 | TTGTAATCCCCACCC[A/G]TCTAGGGAGGGACTG | 9474 |
rs186152343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106243762 | CCTGAACCCAAGAGG[C/T]GGAGGTTTCAGTGAG | 9474 |
rs186192131 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106325075 | AGTGTCTTGCCAACA[G/T]AAAATGTCTTTGGTA | 9474 |
rs186200293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290098 | CTGTGAGTGGTACAG[C/G]TCAATGTAACCTCAA | 9474 |
rs186238415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263090 | AGCAAGCTAAGAACC[A/T]CTGGCTTGAAACTCT | 9474 |
rs186251394 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATG5 | GRCh38.p7 | 6:106216581 | GGGCTGGAGGGAGGG[A/G]GAATGATATAAGTGA | 9474 |
rs186264100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223535 | ACAGGACTCAATTTA[C/T]CTATTTCTTTTAAAA | 9474 |
rs186273196 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327731 | TTGGGGGAAACTATG[C/T]ATGAAGAAACCCAAT | 9474 |
rs186281290 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292653 | TTTCAAAACTTTAAA[C/T]TTTATTTTTTATAGA | 9474 |
rs186295996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306980 | TTAAAGAAAGAATGC[G/T]ATAACAAGACAACTG | 9474 |
rs186301939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283631 | TAGCACACTACGGCC[A/C]AGAACTCCTGGGCTC | 9474 |
rs186308335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300065 | CTAAGCCCATTCTTA[C/T]ATATGAAAAAGTTCA | 9474 |
rs186314154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106322704 | ATGTTGAAATGCCCC[A/G]GGACTCAGTCCTTGA | 9474 |
rs186322585 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106223442 | AGGAAGCAATTTAAG[A/C]CTAAATTGCCTAAGT | 9474 |
rs186327589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242829 | TCCTGACTTTTCTGT[A/C]AGATGTTATTGCAAG | 9474 |
rs186329115 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106262856 | GCAATCTGCAGATCA[A/G]GAGATTCCCTCATGT | 9474 |
rs186352423 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106203856 | GACAAGGTTTTGTTT[C/T]TGTCTTTTAATGACA | 9474 |
rs186362092 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106235980 | TGTCCCTTACTGGTT[C/G]GGTCCATCTCTACTA | 9474 |
rs186392036 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198789 | TGGGAAAAAAAAAAG[A/G]GAGAGAGTGAGAAAG | 9474 |
rs186490714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324784 | CACAACATCGTTATT[C/T]TCAAATTCAAAATTC | 9474 |
rs186497757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278776 | GACAAGGAGGCAACA[C/T]GACTATGTGCTTTGC | 9474 |
rs186507618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106297673 | AAGTTGTTATACACT[A/G]TTCCTTTATTCTAAA | 9474 |
rs186513719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317174 | TCACAATACACGATA[C/T]GAGTAAATGCTGAAA | 9474 |
rs186680544 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106193807 | GACAATAATTGTACT[A/G]TTTACATATGGTCAG | 9474 |
rs186690227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261872 | GCATCTAGTCTGTAG[A/G]GGCCAGAAGTGCTGC | 9474 |
rs186693753 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106233154 | GGTTTCCAAACCAAA[A/G]GCTCAGCTCTGCTCA | 9474 |
rs186757897 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ATG5 | GRCh38.p7 | 6:106323431 | AGGCTCATGCCACTA[C/T]GCCCAGCTAATTTTT | 9474 |
rs186898940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241666 | CTGAGTACAGCAGAT[C/T]ACCATCCACAATGTA | 9474 |
rs186914784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106213627 | TCAGTGGATAAGGAG[A/C]GAAAAGTGGACTAAA | 9474 |
rs186918369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106273753 | CTTATTCTACTATAA[A/G]CAGAAGTAGTAAAAA | 9474 |
rs186924118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294186 | CAAAAAGAAGACTAC[C/T]TGGTGTTATACACAG | 9474 |
rs186940494 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106234016 | TTGCATGCATGCAAA[C/T]ACTCATTATTGGACA | 9474 |
rs186944072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316610 | AGCTTCACCTATACC[A/C]TGTGAATCCTGACAG | 9474 |
rs186945878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106214169 | ATTTTACATCACATG[A/G]TTTTCAAAAGAAGAT | 9474 |
rs186949080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253113 | TCATACGTAATATGT[G/T]AAACATCTCTGTAAG | 9474 |
rs186955071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106237784 | ATAATCACTGCTTAT[A/G]TAGTTGGTTAGGATT | 9474 |
rs186978490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194517 | AAAAAAATGTGAATA[C/T]ACCATTTTTTCTTTT | 9474 |
rs186979131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278534 | TCACCTTTACTGCAT[A/G]TAAGTTCCTCAGTAA | 9474 |
rs186983520 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106231070 | GGAGATAGACAAAGG[C/G]GTAAACAACTAACCA | 9474 |
rs186984907 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293681 | ATGTCAACATTTTCC[C/T]AAGCCACTGAATATT | 9474 |
rs186986745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106217043 | GTATTTGATTTATAC[C/T]TATGCATCATACCTT | 9474 |
rs186994364 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106249191 | TTAGTGGTTTTCAGT[A/G]TATTCAGAGTTCAGA | 9474 |
rs186995998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106298003 | AGAGTCTCGTTCTGT[C/T]GCCCAGGATGGAATG | 9474 |
rs186998988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268505 | CAGAAATACCATTTG[A/G]CCCAGCAATCCCATT | 9474 |
rs187018868 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184860 | GTCAAAACATCAAGG[A/G]GGAAAATCCCCAAAA | 9474 |
rs187020933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211531 | CTGGCCAACATGGCG[A/G]AACCTCATCTCTACT | 9474 |
rs187021905 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106252162 | ACAAAGACTAAGTAG[A/G]AGAAAATTAAAACTA | 9474 |
rs187028993 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190401 | TGACTTAAACACCCC[C/G/T]CAAAAAGCCTCACCT | 9474 |
rs187129104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297590 | ATTTTAGATACCTTT[A/G]AAACTAGAAAAATAT | 9474 |
rs187135348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317705 | ATCATTCCACACTGA[C/T]AGGCTACAAATTCAA | 9474 |
rs187138709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291076 | TCATTCTTTCAAGTA[A/C]AATAATGGTGTTTCA | 9474 |
rs187161189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257554 | CATCATAATGCAGAG[C/T]ATGATTGTACATTCA | 9474 |
rs187203896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313464 | ATCATGATTTCCTCT[A/G]GAAACAAGTCACAAA | 9474 |
rs187225306 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106272435 | CCTCCTTACCACTCT[C/T]GATCTTGATCACCAC | 9474 |
rs187231867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106275751 | ACCCAGTTCTGAATG[C/T]GTAACATTTTGAGTC | 9474 |
rs187241427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106314427 | CCGAGCATGATGGCA[C/T]ATGCCTATAATCCTA | 9474 |
rs187288093 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106204905 | TTTCTCATACAAGTT[C/G]AAACCAAGAACAATA | 9474 |
rs187300978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244225 | GCTAGGTTGTTTCTA[C/T]GAAGATTCTCTAAAT | 9474 |
rs187301308 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106224048 | TATATGATATGAAGG[C/G]CTGGGGCATATGTGA | 9474 |
rs187485089 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308253 | ATATTGTATGAGCTA[A/G]ACTAATGACTTCTAT | 9474 |
rs187511601 | snp | C/T | 0.000462168 | 0.0151944 | intron-variant | ATG5 | GRCh38.p7 | 6:106201946 | AGAAAATGAAAGAAA[C/T]GTTTTAATGTTGCTG | 9474 |
rs187511626 | snp | C/T | 0.00015098 | 0.00868719 | intron-variant | ATG5 | GRCh38.p7 | 6:106248121 | TGAGGCTTTCATAAA[C/T]GGATGTTTTTTAAAA | 9474 |
rs187516570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106267520 | GAACCAAAAAAGAGC[C/T]TGTATAGCCAAGACA | 9474 |
rs187518185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219528 | TAACTACAGTATAAC[A/C]ACTATTTTCACAGTG | 9474 |
rs187519250 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106240449 | GCAATTTACAGAAAA[C/T]CAAGTCCAAATGGTC | 9474 |
rs187519426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290185 | GTGCATGCCACCATA[C/T]TTGGCTTATTTTATT | 9474 |
rs187519942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189832 | AAAAATGTTACTGTA[C/T]GCCTCTCCCACTCAG | 9474 |
rs187532082 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229923 | ATTAACTCAAAAATA[C/T]TAAAGTATGGGGCTA | 9474 |
rs187541041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244465 | TACTTACAACGTCCC[A/C]CTTTGCCTACAAAGC | 9474 |
rs187551809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264186 | ACACAGCACAAGAAC[C/T]TTGTGAAGCATATAC | 9474 |
rs187553417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285021 | AAAAATATTTCTTCT[G/T]ACCCATTCTCTCTCC | 9474 |
rs187567268 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106224701 | ACAAAGATGGAGAAA[A/C/G]CCTGTCTCCCCTGTC | 9474 |
rs187680470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285918 | CTCTGATGTATGATC[C/G]TTACTCCAAAATCAT | 9474 |
rs187711070 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244559 | TTTCCTCAAGGTAGC[C/G]TTCTCTCCTCCCAAA | 9474 |
rs187718995 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106313860 | TTTTCTTCCTTGTAC[A/G]TATTAACTTACACTT | 9474 |
rs187740584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106303582 | CCCGTATAACCCTAA[C/T]GCTAAATCAGACAAT | 9474 |
rs187741813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194136 | AAGGTACAGAGATAC[A/T]AGTTCCTTCTAATTC | 9474 |
rs187749255 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323058 | CCAGTGGCTGGGACT[A/G]CAAGCGCTTGCCACC | 9474 |
rs187788791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259457 | GATATCTGAATTGCA[C/T]TACTCTACTGAGTAC | 9474 |
rs187790234 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210647 | ATGGCACTTGATGAC[A/G]ATGGATTCAGCTTAT | 9474 |
rs187792080 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318411 | AATGAATGACCAATG[C/G]TGCTTCTGAGTCCCT | 9474 |
rs187811307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219207 | ACTACATTGGATTTC[C/T]GGGTCTTCAGCTCTG | 9474 |
rs187977990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304613 | CATTTATATGGCATT[C/T]TGAAAAAGGTAAAAC | 9474 |
rs187978668 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326584 | TCCGTCTCAAAAAAA[A/T]AATAGTAATAATTGG | 9474 |
rs187997751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106225102 | TTTAATTTATTATGT[A/G]CCAGGCACAATAGTT | 9474 |
rs188005966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106265444 | TATTACACAGATCAA[C/T]GAGACATAAAATTAA | 9474 |
rs188029439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296020 | GAAGCTTGAACAAAG[C/T]ACATAATAAACAACT | 9474 |
rs188032593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302625 | ACAATCTAGAGGCTA[C/G]ATGATGAGGGAATCA | 9474 |
rs188037273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106316007 | GAATTAGCTGTATCT[A/G]AAACGTTACATAATG | 9474 |
rs188068437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263710 | TGGTGATACCCAGGC[A/G]AACAGGGTCTAGAGT | 9474 |
rs188075661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235034 | TTAATCAATCCTGAA[C/T]TGTCACAGAGAAAGT | 9474 |
rs188076304 | snp | A/G | 0.00157023 | 0.0279762 | intron-variant | ATG5 | GRCh38.p7 | 6:106279837 | CTCTATCAAAGGAAA[A/G]AATATACATATAAAA | 9474 |
rs188102328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239753 | CACTGGCCAAATTGT[A/G]GCCTCTGCCTATTTT | 9474 |
rs188129978 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106200756 | AAGTGCTAGGATTAC[A/C/G]CGTGAGCCACCACAC | 9474 |
rs188257923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309558 | TTTTATAAAGAAATA[A/C]CTGTGATTAGTGAAG | 9474 |
rs188261120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106257150 | CCACCTCCACATCTT[A/G]TCCCACTGCAAAGTC | 9474 |
rs188265269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276887 | AGGAGGTGTAAATTA[C/T]TGTAATCATTTAATA | 9474 |
rs188278459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106197870 | CATCTAGTTTTTAAT[A/G]TTCTTTAAAGTACTA | 9474 |
rs188293558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106235482 | CCTGTTGAGTGGGGG[A/G]ACTGAGAGACAGGAT | 9474 |
rs188295651 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106215995 | CTAGTTAAATGCATG[A/G]AAAGATGTTTAGCAT | 9474 |
rs188296107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106195513 | CAATTTTTTTTAATA[C/T]GTAATAAAAAGAAGA | 9474 |
rs188347089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214662 | AGTGCCAAATGTACT[C/T]TGTCATACAAACACT | 9474 |
rs188355537 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284637 | TGGGATTATAGGCAT[A/G]AGCCACCACACCCAG | 9474 |
rs188357899 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106254395 | ACTTTATCTTCAGCC[C/T]TAGAAAGTTCTACGT | 9474 |
rs188479764 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312661 | ACACACACACACACA[C/T]AAAAACCAGACAGGC | 9474 |
rs188483457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317941 | TATGCAGTTGTTTCT[A/G]CAGCCATGATACATC | 9474 |
rs188512548 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319755 | TGTAATAGATTCCGT[C/T]AGGGAGAAGGATCAT | 9474 |
rs188514541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271250 | TGACTTCTCAAAACA[C/T]ACCTATTGTGGACTG | 9474 |
rs188518383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280472 | TAAGCTTACTATAAG[G/T]CAATTAGACCTCAAT | 9474 |
rs188520596 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106292753 | GGGATTACAGGCGTG[A/G]GCCACCAAGGCTGGC | 9474 |
rs188549416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296737 | ACAGGTGAATTACTT[C/G]AACCTGGGAGGTGGA | 9474 |
rs188559112 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316523 | TATTTAAGTACTGAA[A/C]CACAGTCAAAATGAA | 9474 |
rs188572020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209953 | GGATCTTATTAAAAT[A/G]TAGATTCTCAGGCTG | 9474 |
rs188640680 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106213815 | TTGAACAATTGATGT[C/G]ATAATTAAATGAGAT | 9474 |
rs188737513 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228414 | CGCGGCTAAGTGCCC[G/T]GGTTCATCCTAATTG | 9474 |
rs188743477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246258 | AGCAGGAGGTTCTGC[C/T]GAGAGTCCCCATCTG | 9474 |
rs188745597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265914 | GATCTAAAATCGACA[A/C]CCTAACATCACAATC | 9474 |
rs188753666 | snp | C/G | 0.0209421 | 0.100162 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184467 | TTTTAAATAAAGACG[C/G]ACACAACATTTATTT | 9474 |
rs188764193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207210 | GGTAATGGCTGGCTG[C/T]TCCCATCTCTCCTCT | 9474 |
rs188784817 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106259873 | CCAAATGTCTATCAA[C/T]GATAGACTGGATTAA | 9474 |
rs188807514 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106298280 | TGTCAAAATCTTAAA[A/T]TTTTTTTTTAAATTT | 9474 |
rs188836267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106308800 | ATACTATTTAGGATA[C/T]TTATTGGTTCTATAA | 9474 |
rs188839793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188928 | TTATTTTCTGACTTG[C/T]CTCAATAACACAATT | 9474 |
rs188861924 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106230625 | TCATCGGAAAATGAC[C/T]AGTGGTGCTGGCATC | 9474 |
rs188872749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267642 | GGTACCAAAACAGAT[A/C]TATAGACCAATGGAA | 9474 |
rs188886112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205536 | TAATTGCAACTATTA[A/T]GTATCCATAATAATT | 9474 |
rs188891854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233962 | CACCTTCACTGCCCA[C/T]ACCCATATGCCCCAC | 9474 |
rs188942429 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327190 | TGTCAGACAAAAGTA[C/T]ATAAAATTTCCTTTA | 9474 |
rs189064886 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106324914 | TTTGGAAGTTCAGCT[A/G]CTGTCTGGTAAGTCT | 9474 |
rs189110572 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106290426 | CCTGGGCTAAAGCGA[A/T]CCTCCTGCCTCAGCC | 9474 |
rs189134612 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326454 | CGGTGGCGGGCTTCT[A/G]TAGTCCCAGCTACTG | 9474 |
rs189137764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106215302 | ACCCAGGGAAAAGTG[A/G]TTCTAAACCTGGGCT | 9474 |
rs189138553 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248750 | TCCTGACCAGCCTGA[C/T]CAACATGGAGAAACC | 9474 |
rs189139749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106196812 | CCAACTAATTTCTTC[C/T]CACTCTAGGCACTCC | 9474 |
rs189168984 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ATG5 | GRCh38.p7 | 6:106269482 | TCAGGGAGGCTTGGC[C/T]GCACAGGAGCCCATG | 9474 |
rs189176917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241780 | CCTTTGGACTCAACT[A/G]CAACTCTTCCTTGAG | 9474 |
rs189177061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106222903 | TGGTATTCAATAAAG[A/C]GCAATAAATGTTAGC | 9474 |
rs189183652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291535 | ACCCGACACACAGAA[G/T]GATCTCCATATTTGT | 9474 |
rs189191304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106262206 | GCCTCCTGAGTAGCT[C/T]GGATTAGAGGCGTGT | 9474 |
rs189191490 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106310244 | CAGAGCCAACAACTG[C/T]AATTTTAAAAGAATA | 9474 |
rs189215894 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106203659 | GTCACCCAGGTTGAA[A/C/T]TGCAGTGGTGCAACC | 9474 |
rs189347791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106205966 | AGTACCTTTAAAAAC[A/G]TAATATTCTTATTCT | 9474 |
rs189378076 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106240968 | GACCAGCCTGGCCAA[C/T]ATGGCAAAACCCTGG | 9474 |
rs189380562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260279 | AAAAAGAAAAAATAG[C/T]CACAAAATCTTGACA | 9474 |
rs189388204 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106221444 | TAGTCCCAGCACTTT[G/T]GGAGGCCAAGATGGG | 9474 |
rs189395188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106281152 | GAAAGCAGGAATTAA[C/T]TGAAAGTGATTAAAG | 9474 |
rs189396568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324440 | CAATCTCCCACAGAT[A/G]CCGAGGGACAGGAAA | 9474 |
rs189399101 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106202811 | GGACTACAGGAGTGC[A/G]CCACCATGTCCAGCT | 9474 |
rs189413314 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106192397 | CAATCTGGGTTTTAG[A/G]TCTTATTCAACTAAG | 9474 |
rs189421832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106221060 | GGAAACTAAAGCCCA[C/T]GTCAACCAATGAAAA | 9474 |
rs189423275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106266387 | AAGTCCAGGACCAGA[C/T]GGATTCACAGCTGAA | 9474 |
rs189427079 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106288268 | AGTCACTGCCCTGCC[A/G]CACAATTAATTTTTC | 9474 |
rs189435235 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106306629 | AAAACTGAAAAGCCC[C/T]GCTAGTCACACAAAA | 9474 |
rs189454658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106246981 | CTTCATGAAAAATAT[A/G]GACTATTTGAAAATT | 9474 |
rs189479678 | snp | A/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327761 | TAGGTGAAAGGTGAT[A/T]ACTTGATTTGACTTA | 9474 |
rs189529718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299240 | CTACACACATTCTCC[C/T]GTATACTTTAAATTA | 9474 |
rs189565075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261564 | GCAGTGATAATTCAC[G/T]TGAAGTACCCAGAAC | 9474 |
rs189607296 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106236286 | ATTATGAATAATTCT[C/G]CTATGAACACTTCTG | 9474 |
rs189610981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305726 | CTTCCAACACTTCAG[C/T]GGTAGCTGCTTTCCT | 9474 |
rs189631360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278089 | GACTGTCGGCACATG[C/T]GACCATGCCCTGGCT | 9474 |
rs189675509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203220 | GTAATTTATTGCTAA[C/T]AATCTCATTGTTTTA | 9474 |
rs189704486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106278870 | TGACATAATTTATCA[C/G]CGATCATAAGCTCAT | 9474 |
rs189715358 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106297874 | CCAGGAGTTCGACAC[C/T]AGCCTGAGCAACATG | 9474 |
rs189725563 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317341 | GAAAACACTCTAAAT[A/C]ATCTTACGAGTTTAG | 9474 |
rs189736910 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218096 | AATGCAAAAGAGACT[C/G/T]TGGTAAGGGGTTGAG | 9474 |
rs189744426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238960 | TTCATCAAACTAGCA[A/G]ATAACTTAGTATCAT | 9474 |
rs189744650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258581 | ATATAGCTCTCCTCA[C/T]TGTAGAGAGGAGAAA | 9474 |
rs189831718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241323 | ATGCATTAGGATGGC[C/T]AGTATGAAGAACAGA | 9474 |
rs189841508 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106281597 | ATAGACACTGGGATT[A/G]TTTCTAGATACTGGC | 9474 |
rs189850740 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185770 | TAATTGGCAGCAAGA[A/C]ATTCTATGACAGCTT | 9474 |
rs189865442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106282995 | GAGGTCTCCCTATGT[C/T]GCCCAGGCTGGTCTT | 9474 |
rs189872051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287037 | TAAGCTGGTGGTAAT[C/T]TGTCAGACAATAGTA | 9474 |
rs189886384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320621 | CAAGTCAAAAGGCTG[C/T]TCTGAAAAAAAAAAA | 9474 |
rs189886693 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106257506 | TAATCTTAAGGGACC[A/G]CTATCATACATGCAG | 9474 |
rs189892859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323545 | CGCCCGGCCAAGTTA[C/T]ATTCTTTAGTTGCTC | 9474 |
rs189906998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216656 | CTGAAATTTTATCAC[A/G]GGAATGGTTGCACAA | 9474 |
rs190058224 | snp | A/G | 0.00479805 | 0.0487443 | intron-variant | ATG5 | GRCh38.p7 | 6:106250989 | CCAATGTCCAGATAC[A/G]CAAGTCTCTCAGCAA | 9474 |
rs190087805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106193120 | TTAAGAGCACACTAC[A/G]TGATGTAGCAGTAAA | 9474 |
rs190095869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106232885 | TGTACATCCTGACTC[C/T]CAATTCTTATTTGCC | 9474 |
rs190100906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106213196 | ATGCATTTACCAGGG[C/T]ATCACTATGCTAATG | 9474 |
rs190109473 | snp | A/G | 0.000881655 | 0.0209774 | intron-variant | ATG5 | GRCh38.p7 | 6:106248099 | AGAGTGCTTCAATTA[A/G]GATGTCTGAGGCTTT | 9474 |
rs190113637 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106267294 | CTTACAAGTGACATG[A/G]AGGACCTCTTCAAGA | 9474 |
rs190123015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106211618 | AGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 9474 |
rs190125807 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106290117 | ATGTAACCTCAAACT[C/T]CTGGGCTCAAGTGAT | 9474 |
rs190129804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106299908 | CTGATTCACTGGAAA[C/T]GGGATTACATTTCAT | 9474 |
rs190134556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209476 | TAACATTAGTGAAAT[C/G]ACAAAAATTTTAGAA | 9474 |
rs190135393 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249523 | AGTAGTTTCCGCTTT[C/T]TATCTATTATAAATA | 9474 |
rs190140641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106187528 | AGAACCATCAAGAAA[C/T]TTTGTGTTATTCCTT | 9474 |
rs190140881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229753 | AAATCCTTAACATCC[A/T]GTGACCTGCGGATGG | 9474 |
rs190207701 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185027 | CACTTTCGTTTACAT[C/T]AACCAATTATTTTCT | 9474 |
rs190351840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293187 | AATTTCCAACACATA[G/T]TTTAACACCAAATGT | 9474 |
rs190357737 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244377 | GATACAGAGAAAACT[A/C]GTTAATATGGCCTGA | 9474 |
rs190359689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263807 | ACATCAACATAAAGG[A/G]CCCCCACAAAAAAAC | 9474 |
rs190363902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313399 | TAAGGATACATAAAC[A/G]GATCGCTGCCTAATG | 9474 |
rs190364895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106229130 | TCTACTTCCTCTGAT[C/T]CCTGCCTCCTAGGTA | 9474 |
rs190364929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106256062 | TCACTCAGAAAGCAA[A/G]CCAAAGTCATAAGGT | 9474 |
rs190368144 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106231813 | AATAGAGATCAGGAT[A/G]AGCAGGCAGAATGGG | 9474 |
rs190368480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284773 | AGTTATGCTGAACAT[C/G]TTTTCATGTGTTTAC | 9474 |
rs190379283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295424 | TAGATAAGATTCACT[C/G]GAGATCACATAAAAT | 9474 |
rs190398620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317784 | CACAAAATTAACTCA[C/T]TGAAAATAGGAAAGA | 9474 |
rs190403981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106191229 | CTAGAATGAATCTTA[C/T]GATCATACCAGTGTA | 9474 |
rs190417765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271018 | CTAGAGCCACTTTCA[C/T]TCTGGACTCCTATTC | 9474 |
rs190448157 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106235305 | TGACTAAGATCTACC[A/G]TGGACCCCTGGACCG | 9474 |
rs190460450 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106232599 | GGCAGTACCCCCTTA[C/G]ACCCGAGGCTCAACA | 9474 |
rs190590151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315577 | TTACATATTAGCTCA[C/T]ATATAACATACAATA | 9474 |
rs190621228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276276 | GAGACCATCCTGGCT[A/T]ACATGGTGAAACCCC | 9474 |
rs190621253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207685 | GCTGAAAATCAGACA[A/G]TGTATGGACTTTAAG | 9474 |
rs190665229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250676 | TCATGCATACTTAAA[A/T]TTTTACTTTGCTGCC | 9474 |
rs190674688 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327421 | AACAAAATGTTGGGA[A/C]CAGGCACAGTGGCTC | 9474 |
rs190675915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289312 | GGCCTACATCAATCA[A/G]TACAAGCTATCAATT | 9474 |
rs190685050 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106212411 | TTTGGGAGGCCAAGG[C/G]GGGCGGATCACCTGA | 9474 |
rs190797312 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106290331 | TCTTTCATTCGTTCA[C/T]TTATTTTTAGAGAGA | 9474 |
rs190801587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106308515 | AAAATTTGTAAAACC[A/G]TATTTATTTACTAGT | 9474 |
rs190825454 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325752 | CCAGCGAATACAACC[C/G]GCAACGCTGCGGAGC | 9474 |
rs190831357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267557 | AGCAAAAAGAACGAA[C/G]CTGGAGGCATCATGC | 9474 |
rs190889396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106208699 | AACAGCTAAGCTTTT[A/G]TTCTGCAAAAGATCC | 9474 |
rs190899085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247725 | TAAAAAGCACAAAAA[C/T]GTAAAAGCATGGCAC | 9474 |
rs190921450 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267100 | TAGAAAACCCCATCG[C/T]CTCAGCCCAAAAACT | 9474 |
rs190931876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306754 | CCACACTGTTTCCCC[A/G]TCCATCCTGTCATTC | 9474 |
rs190987281 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106238374 | TATTAAAGACAGCTT[A/T]CCCCAAATATTACTG | 9474 |
rs190992708 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217225 | TAAAAATTGTATAGC[A/G/T]TCATGGTGATTTTAA | 9474 |
rs191035111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106199369 | TGATGTATCTACCCA[A/G]TGGAGTATTATTCAC | 9474 |
rs191036835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234010 | CACTCTTTGCATGCA[A/T]GCAAATACTCATTAT | 9474 |
rs191047304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106283865 | TGACTTGTGTTTTCA[C/T]TGAATTTGTCCATCT | 9474 |
rs191050873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300177 | TCCTTTATGCCTAGT[G/T]TTCCATTATTGGAAC | 9474 |
rs191074751 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243093 | TCCATTTTCAAAAAT[G/T]TACTTTTTCTCTCCC | 9474 |
rs191077559 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213881 | GACTAGTTCTTTTCA[C/T]TCCTCTCTTGAACCA | 9474 |
rs191080215 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106262931 | AGCCATTTGGGCAGA[A/C]ACCGAGCTAGCTGCA | 9474 |
rs191081881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106194348 | CGAGATACTAACAAG[C/T]TTCAATTTTGTCCAA | 9474 |
rs191092671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299134 | GGTCCACCCTTGGTA[C/T]GTGTGGGGATTGGTT | 9474 |
rs191098841 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106319137 | AGCACTTACCACATT[A/G]GATACAAGAATTAAA | 9474 |
rs191104164 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106263222 | ACAGTGCTAAGGAGT[C/G]TGGGAGGTCTGGACT | 9474 |
rs191115133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241010 | ATACAAAAATTAGTC[A/G]GGCATGGTGGTGGGC | 9474 |
rs191119204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106260987 | GACACCTGGAAATGC[A/G]TAATACATGAACCAG | 9474 |
rs191129926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301379 | AATTGATATAAGCAA[C/T]TAGAGAGAACAGATA | 9474 |
rs191135549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281481 | CATATTTTTGAGATT[C/T]ATTCCTGTTACTACA | 9474 |
rs191136158 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106223762 | GAAATATTTAAAAAT[A/T]GCTCATGATATCCTC | 9474 |
rs191140604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200089 | TGTTCATTTTTAAAG[C/T]ATTACATACATGTAG | 9474 |
rs191148337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229502 | GAGAGACAAAGAGGA[G/T]AAAGAGGCAGAGAGA | 9474 |
rs191205361 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106322864 | TTCCATTTAGAAATT[G/T]AACATATGCAAAACG | 9474 |
rs191239203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198881 | ATAAAGAACTTGTAT[C/T]CAGAATATATAAATA | 9474 |
rs191306142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106189941 | CTTCTTTATATAGGG[C/T]ACTTTTTAGAGAGTA | 9474 |
rs191318992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210790 | AGTATATACCTCATA[G/T]ATTTTTTTGTGAAGG | 9474 |
rs191330176 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106322994 | GCGCAATCTCGGCTC[A/T]CTGCAAGCTCTGCCT | 9474 |
rs191361326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106307651 | AAGCATTTCTCCTGC[C/T]TCAGCCTCCCAAATA | 9474 |
rs191362619 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284481 | CAGCCTTCCAAATAG[A/C]TGGGACTATAGGCAC | 9474 |
rs191384431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106204778 | CCCCCACAAGCCATA[A/C]GGAACTGTGAGTCAA | 9474 |
rs191394254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106243816 | AGCCTGGGCGACAGA[C/G]CAAGACTTCATCTCA | 9474 |
rs191416354 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ATG5 | GRCh38.p7 | 6:106323021 | GCCTCCCGGGTTCAT[A/G]CCATTCTCCTGCTTC | 9474 |
rs191464941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106251588 | AAACGCTATATTCTT[A/G]TATTAAAAAGGTATT | 9474 |
rs191583933 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106325129 | AGGGAATATCGTAAA[C/T]AGATAAATTGCTTGG | 9474 |
rs191655264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302651 | AATCAAGAGTGGAGA[C/T]GAACATCAACAAATT | 9474 |
rs191690703 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106274861 | GGCTAACTGATAGGC[A/C]AGCAAAATACATAAA | 9474 |
rs191701369 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294581 | CCAACACTTTGGGGG[A/G]CCAAGGTGGGTGGAT | 9474 |
rs191709982 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314062 | ACCAATTACCTATAA[A/G]ACAAGACAATCCTCT | 9474 |
rs191712322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213668 | TATAGAGCTTGGAAT[A/G]TCAAATGTAGTGGAA | 9474 |
rs191718121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233174 | AGCTCTGCTCACAGC[A/G]GGTTAAATACTTAGG | 9474 |
rs191718492 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106234496 | AAAATTTAGCAATAC[G/T]GTAGACACAACCAAC | 9474 |
rs191718725 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184077 | GCCTCTTGTGCAAAA[A/G]TATAAGTCAGTGGAT | 9474 |
rs191720608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214395 | TAGGAGAGTTGAAAA[C/T]AAGCACTTTCTGTAC | 9474 |
rs191733863 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106271950 | TCTGCCTAGGAAGTT[C/T]TTAATCCCAGATAAA | 9474 |
rs191735414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206902 | AAATCTCCACAAATA[G/T]GAATGCTGTAAACGT | 9474 |
rs191735570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106253482 | TGGACAGTAACTGTC[C/T]GAAAATTAACTGAGA | 9474 |
rs191799403 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106190662 | CTTAAAAGTGAACAT[A/T]AAAAAAAAGTTACGT | 9474 |
rs191904079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268639 | CCCAAATGCCCATCA[A/G]TGTTAGACTGGATAG | 9474 |
rs191912906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106297595 | AGATACCTTTAAAAC[C/T]AGAAAAATATGAAAT | 9474 |
rs191914914 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106291158 | TTCCTCAAGACAACC[A/C]TATTTGGCATGCAAC | 9474 |
rs191922942 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ATG5 | GRCh38.p7 | 6:106309633 | TTTCCCCCACAGGAA[A/G]TATTATCGCCCCTGT | 9474 |
rs191926815 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106189482 | TAGCTTTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 9474 |
rs191930995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231105 | ATGCCAATATTCCCC[A/G]ATTATGCCCCCTCCA | 9474 |
rs191934410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211578 | AGCCGGGAGTGGTGG[C/T]GTGCATCTGTAGTCC | 9474 |
rs191936266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257774 | TACATGGTAGCTACA[C/T]GGAAAATACCTCTAT | 9474 |
rs191939122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249232 | CATCCCAAAAAGAAA[A/C]CTGTAACTATTAATA | 9474 |
rs191939935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229936 | TATTAAAGTATGGGG[A/C]TATTCTGTCAGAAAA | 9474 |
rs191953392 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106314648 | AATATACTCTTATAC[A/T]CTCACATACTCTTAT | 9474 |
rs191958368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205186 | ATGACTGGTGAGAGG[C/T]TGACTGAATACAGCA | 9474 |
rs191981177 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106272991 | TGAGACTGAGTGACC[A/G]ATATAGATTCATTCT | 9474 |
rs191983549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224284 | ATGGAGGGAGAAAAA[A/G]CAGGTAGAAAAATCT | 9474 |
rs191984595 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106194002 | CTTCTTGAGATTAAG[A/G]TAACAATAATTCAGA | 9474 |
rs192018128 | snp | A/C/T | 0.0142994 | 0.0835679 | intron-variant | ATG5 | GRCh38.p7 | 6:106203876 | TTTTAATGACAGAGG[A/C/T]ATACCTCAACATATT | 9474 |
rs192127768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313556 | TTAAATGAACATAAA[C/T]GAAAAAATACAAATT | 9474 |
rs192137964 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326501 | AGAATGGCGTGAACC[C/T]GGGAGGTGGAGCTTG | 9474 |
rs192164605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290608 | AGGTGTGAGGTATCA[C/T]GCCCATCCAGTTTAT | 9474 |
rs192192917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221070 | GCCCATGTCAACCAA[C/T]GAAAAATGGGAGGAC | 9474 |
rs192195600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248872 | GAACCTGGGAGACAG[A/C]GGTTGTGGTGAGCCG | 9474 |
rs192214620 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106278727 | TTTTTCAATTATCCA[C/T]TTTTATAAAATGTTA | 9474 |
rs192220155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248339 | AAATATCCCTCTAGA[A/C]GTTTCTGAAAGGACA | 9474 |
rs192232108 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316653 | GGATCATTCTCGCAT[C/T]TACCCCTGCCCCGTC | 9474 |
rs192248610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291821 | AAATGAAATTCATGC[A/G]TACCAACACTATGTG | 9474 |
rs192254459 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327245 | ATTTAGGGGCGCATA[C/G]ATGGATAAATATGTG | 9474 |
rs192260322 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106210193 | CTCAAGACTCAGGTA[G/T]CAGGAAAAGCCCCTT | 9474 |
rs192260660 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106310691 | ACTGTACGTATTAAA[C/T]AGTAGCTCCCCATTC | 9474 |
rs192310750 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106252575 | TGCAGGAAAAAGTGA[A/T]AACTTTAAAGGATTT | 9474 |
rs192318927 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223506 | TCAAAACTTGCTGTG[C/T]TGGGCTGCCCCCTAC | 9474 |
rs192404910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106304666 | GTAATTACTGTGAGT[C/T]GGGGGAAGGAAGAGG | 9474 |
rs192407929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260105 | CACACTGAGGCCTGT[C/T]GGTGGGTGGGGGCCT | 9474 |
rs192429625 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106202527 | TGGGATAAATGGGGA[A/G]ATACAGAATGGACAA | 9474 |
rs192440337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240577 | GAGTTATAATGCCCT[A/T]TTGCTGGTGGAGATG | 9474 |
rs192441054 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106220518 | AAATAAAGATAGGAC[A/T]TTAGTCTTTGTATTT | 9474 |
rs192494998 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106293812 | AAATAAACATGACTA[A/C]TACAAATGTTGTAGA | 9474 |
rs192557976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309371 | CATGGGAGTCCAAGA[A/T]AATAGGTACCAACCA | 9474 |
rs192580662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202864 | GATGGGGTTTCACCA[C/T]GTTGCCCAGGCTGGT | 9474 |
rs192588697 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106230692 | AAGGCAAAAACACCC[C/T]TAAGATGTATTCTGG | 9474 |
rs192602661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106267938 | GGCATGGGAAAAGAC[C/T]TCATGACTAAAACAC | 9474 |
rs192635380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226146 | GGCCCCTGGCAAAGA[C/T]TGGAAGATACTCTAG | 9474 |
rs192645148 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106265507 | ACCAAGTGGACCTAA[C/T]AGACATCAACAGAAC | 9474 |
rs192653370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256279 | CACAAGCTTTCAAAA[C/T]AAAGGGGCCACCAAT | 9474 |
rs192658334 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ATG5 | GRCh38.p7 | 6:106303964 | TAGAAGTTCTAGCTA[A/C]TCCAATAAGGAAAAA | 9474 |
rs192666238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323244 | GGTCTTTTCCGTTTC[A/G]CTAAGTGGAAAAGTC | 9474 |
rs192681087 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106194783 | CTCAGGTGATCCACC[A/C/T]GCCTAGCTTACCACG | 9474 |
rs192693585 | snp | A/G/T | 0.00358938 | 0.0422398 | intron-variant | ATG5 | GRCh38.p7 | 6:106235320 | GTGGACCCCTGGACC[A/G/T]GCCTACTAGCCCATG | 9474 |
rs192696669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264635 | CCATCAGACTAACAG[A/C]GGATCTCTCTGCAGA | 9474 |
rs192701542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106285155 | TCTATCGATCTGTCT[C/T]TGAGTTCAAAGAACC | 9474 |
rs192710934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106201002 | ATGGCATAATATTTG[C/T]ATATAACCTATGCAC | 9474 |
rs192713232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106239851 | GTTACAGAATCACAC[A/G]GTTTCAACAGAGACC | 9474 |
rs192753151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106286082 | CCACTATCTACTAGA[C/T]CTTGCAGAGTATCAG | 9474 |
rs192763180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323442 | ACTATGCCCAGCTAA[C/T]TTTTTATTTTTTTGT | 9474 |
rs192795563 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106280431 | ACATATAAATTGTGG[A/C]ATAAACTTATTCACT | 9474 |
rs192824222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295384 | AAACACAAAGAACTC[C/T]GCTAGGCAAAATAGT | 9474 |
rs192830110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214782 | TCCCTTTCTTGGGAT[C/T]GAGATCAATTTGATG | 9474 |
rs192838462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106254563 | GCATAGTGGAAAAAG[C/T]AGACAGTCTGGAGCC | 9474 |
rs192867805 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245368 | TGGTCAGGGCAGACT[G/T]CACTTTTCATGATAA | 9474 |
rs192915067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219246 | CTGTTTCTTAACATA[C/T]GTCAATTTTCTATAT | 9474 |
rs192973377 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326755 | ATAATTGGGAACATA[A/G]GGAAAATTCTAGTAG | 9474 |
rs193001041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259609 | TTTCCCTTCATCACC[C/T]TGTCTCTTCTGCTCC | 9474 |
rs193009988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298028 | GGAATGCAGTTGTGC[C/G]ATCTTGGCTCACTAC | 9474 |
rs193028910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106275953 | GTGAATGAGTGTGGC[C/T]GGGTTCCAGTAAATC | 9474 |
rs193046572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235077 | AGATTGAATACAACG[C/T]AGAACAGAGGAGCTT | 9474 |
rs193055927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196555 | ATGGTGAAACCCCGT[C/T]TCTACCAAATATACA | 9474 |
rs193063666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298282 | TCAAAATCTTAAAAT[A/T]TTTTTTTAAATTTCA | 9474 |
rs193102840 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106205693 | TTATATATCTTTTTT[C/T]TCACCCTTTCCCAAA | 9474 |
rs193133305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315609 | CTCAGTGAACGTATC[A/G]TGTGTGTGTATGTGT | 9474 |
rs193142878 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106276353 | CCTGTAGTCCCAGCT[A/G]TTCGGGAGGCTGAGG | 9474 |
rs193145508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244466 | ACTTACAACGTCCCC[C/T]TTTGCCTACAAAGCT | 9474 |
rs193175280 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318128 | CTCAGAAGAAGCAGA[C/T]AGAAAATATAATCCA | 9474 |
rs193232070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280701 | AAACTTTTTATATGG[A/T]TTATCTTATTTAATC | 9474 |
rs193257132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106224846 | AGATCGCACCATTGC[A/G]CTCCAGGCTGGGCAA | 9474 |
rs193296435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295935 | ATCATAAATTATTTT[A/T]TTAACCCTCAATATT | 9474 |
rs199498497 | in-del | -/A | 0.0670745 | 0.170406 | intron-variant | ATG5 | GRCh38.p7 | 6:106229559 | AAAGATAGAAATAGT[-/A]AAAAAAAAACAGTGT | 9474 |
rs199501225 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321361 | CTCTCTGGGTCAACT[-/C]CTTTTTTTTTTTTTT | 9474 |
rs199502012 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | ATG5 | GRCh38.p7 | 6:106243259 | CATTCAATCGTCAAT[-/G]GGAAAGGAAGCAGAA | 9474 |
rs199541397 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295056 | TAAAATTAAAAAAAA[-/AT]ATACATACACACACA | 9474 |
rs199547664 | snp | C/T | 0.00199795 | 0.0315433 | intron-variant | ATG5 | GRCh38.p7 | 6:106293124 | AAAAATGAAACAGTA[C/T]ATTTTGAGAAAATAA | 9474 |
rs199709291 | in-del | -/AAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270427 | AACGTACTACAGGCA[-/AAT]AATAATAATAACAAA | 9474 |
rs199737886 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304077 | ATAGAAAACCCCAAA[-/G]GATCTACCAAAAAAA | 9474 |
rs199741072 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314724 | TTTGGAAAAAAAAAA[-/A]TGGTATCCTAACCTA | 9474 |
rs199767126 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323642 | TGGTCATTTCGCACT[A/C]CCGCCACTATTACTA | 9474 |
rs199772962 | snp | C/T | 0.17461 | 0.238362 | intron-variant | ATG5 | GRCh38.p7 | 6:106312643 | ACACACACACACACA[C/T]ACACACACACACACA | 9474 |
rs199868575 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185092 | CTGGCTATTCTTTTT[G/T]ATTAAGCTTTACAAT | 9474 |
rs199893661 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307533 | GATTTGATTTCAATA[-/C]CCTTTTTTTTTTTTT | 9474 |
rs199897926 | in-del | -/AAGAAGATAGTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259795 | AGCATTAACAAAAAC[-/AAGAAGATAGTTT]AAGAAAAAATAGTTG | 9474 |
rs199949762 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301264 | TCTAATCAGACATAA[A/C]CTCCTTGTAAGCTCT | 9474 |
rs199962964 | in-del | -/ATC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313769 | AGCAAGGGACATATT[-/ATC]TGAACTACAGCTATA | 9474 |
rs200072827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106202576 | TAATGTCAAATTTCT[C/T]AGGTACAATAAGGAC | 9474 |
rs200079794 | in-del | -/AGAG | 0.0178098 | 0.0926698 | intron-variant | ATG5 | GRCh38.p7 | 6:106198787 | TCTGGGAAAAAAAAA[-/AGAG]AGAGAGTGAGAAAGA | 9474 |
rs200119350 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238186 | ATTTACTTTTATTTT[C/T]TAGAGACGGAGTCTT | 9474 |
rs200149714 | in-del | -/T | 0.0364509 | 0.129988 | intron-variant | ATG5 | GRCh38.p7 | 6:106242062 | AGAAGCAAAATGTGG[-/T]TATGTATATACAATG | 9474 |
rs200188519 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277270 | GCAGGTGAAGGTTTT[A/G]TTCTGTTTTATTCTA | 9474 |
rs200320350 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312624 | CTGGCAAAAAAGACT[-/AC]ACACACACACACACA | 9474 |
rs200336924 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208557 | TTTTCTATATGGCAA[-/G]GAAAAAAAAAAGGGC | 9474 |
rs200354473 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271790 | CTTTAAAAAAAAAAA[-/A]TGGTGGGAAATAGAG | 9474 |
rs200357943 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | ATG5 | GRCh38.p7 | 6:106253397 | TGGCAGAAGGTTTCT[-/A]CCCAGGGAAATCTGT | 9474 |
rs200366820 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229466 | CAGGGAGGACAGGGA[G/T]AGAGACAGAGAGGAG | 9474 |
rs200472895 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106306071 | AAAAGTTAACACCCC[A/G/T]AAAACTACCATAAAG | 9474 |
rs200496902 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185873 | AAAAAGTGATCTACT[C/G]TATGTGAGTCAGAAA | 9474 |
rs200527521 | in-del | -/G | 0.0275645 | 0.114116 | intron-variant | ATG5 | GRCh38.p7 | 6:106249198 | TTTTCAGTATATTCA[-/G]AGTTCAGAACATTTT | 9474 |
rs200568129 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277260 | AAAAATTATGGCAGG[G/T]GAAGGTTTTCTTCTG | 9474 |
rs200569483 | in-del | -/TTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234582 | AATATTTTTTGTCTG[-/TTT]TGGTACCTTAGCCTA | 9474 |
rs200570662 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252362 | ATTAAAAAAAAAAAA[C/T]ATGAAAAATACCATT | 9474 |
rs200657500 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259023 | GAAAATATTACTCAG[-/T]TAACTATTCTTTAAA | 9474 |
rs200687385 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293968 | GTTTCAGATTTCAGC[-/T]TTTTTTTTTTTCTTC | 9474 |
rs200695536 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292210 | GAATGAATCACTGTT[C/T]GTGATCAACTAATAT | 9474 |
rs200696325 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309620 | AGAAAAAGCAGTTTT[C/T]CCCCCACAGGAAGTA | 9474 |
rs200751503 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200493 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 9474 |
rs200799919 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276481 | AAAAAAAAAAAAAAA[C/T]AAACTGAAGCTCAAA | 9474 |
rs200809904 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232408 | TAGGGAGAGACATTC[C/T]AGCAAAAGCAGGGGC | 9474 |
rs200813343 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265146 | AAAGAGATTGAGGAA[A/T]ATTTACCAAGCAAAT | 9474 |
rs200823237 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | ATG5 | GRCh38.p7 | 6:106189435 | AGACCCCATCTCTAC[-/A]AAAAAATAAAAAAAC | 9474 |
rs200861048 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106280993 | GGAGCTAAAAATGGC[-/A]AAAAAAACAGCATTT | 9474 |
rs200886825 | snp | A/T | 0.5 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106246396 | CTCTCTCTCTCTCAC[A/T]CACACACACACACAC | 9474 |
rs201054909 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280291 | AAAAAAAAAAAAAAA[C/T]AAAGAAAAGAAAAAA | 9474 |
rs201076319 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233826 | CCCCTTTCACTCTCA[C/T]TGCACCCCCTCCATG | 9474 |
rs201081726 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189646 | TTAATAATAAAACAG[A/T]AAAAAAAAAAAAAAA | 9474 |
rs201085795 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295581 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTAC | 9474 |
rs201114439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106304178 | AAAATGAACATTCAC[A/G]CTCGTTTTGGCAGCA | 9474 |
rs201146845 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266478 | ATAGAAAAAGAGGGA[A/C]TCCTCCCTAACTCAT | 9474 |
rs201148064 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198939 | ATCCATGAAAAAAAA[-/A]CAAGGATTTGAATAG | 9474 |
rs201259155 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263893 | AAAAAAAAAAAAAAA[-/A]CAGCACAAAAATGCT | 9474 |
rs201265668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106292713 | GTCTTGAAATCCTGG[G/T]CTCACCTCGGCCTCC | 9474 |
rs201271861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106322113 | AAAGAAACTCCAACC[G/T]GTGACGCAATCTACT | 9474 |
rs201276950 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106287865 | GCAAGCAGCATGCCT[A/G]TAGAATTAATGAAAA | 9474 |
rs201330760 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106312886 | ATTACAGAAAACTAA[A/C]TGGTAGGAGGTGGAA | 9474 |
rs201386627 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310220 | AGAGATGCCAATGGT[G/T]AAGTGAGGCAGAGCC | 9474 |
rs201431772 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307756 | GGTCAGGCTGGTCTC[A/G]AACTCCTGGCCCCAG | 9474 |
rs201452945 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295063 | AAAAAAAATATACAT[-/AC]ACACACACACACACA | 9474 |
rs201454419 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267129 | TCCTTAAGCTGTTAA[-/G]TAAACTTCAGCAAAG | 9474 |
rs201468168 | in-del | -/T | 0.046775 | 0.145601 | intron-variant | ATG5 | GRCh38.p7 | 6:106235476 | GGTTTTCCTGTTGAG[-/T]GGGGGGACTGAGAGA | 9474 |
rs201513151 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214630 | AATTGTTATACTTAT[C/T]ATAATTCTGTCTAGA | 9474 |
rs201547309 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309615 | TATAAGAAAAAGCAG[-/C]TTTTTCCCCCACAGG | 9474 |
rs201591128 | in-del | -/GAGC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235774 | CCTCCCTTTGTATGG[-/GAGC]TCTCTCTGTCTTCAC | 9474 |
rs201591869 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290429 | GGGCTAAAGCGATCC[A/T]CCTGCCTCAGCCTCC | 9474 |
rs201597983 | in-del | -/TAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246773 | TTCAACTAAATTATA[-/TAT]CAAGTAAGATATTTT | 9474 |
rs201668696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266194 | CACAAAAATACAAAC[C/T]ACCATCAGAGAATAT | 9474 |
rs201699550 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234887 | AAGATCAACTTAACT[C/T]CCTAGCATCAGTAGT | 9474 |
rs201767848 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230940 | ACTCGCAATTATGTA[A/G]AAAGTGTGATTTATG | 9474 |
rs201789611 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267417 | GGCCATACTGCCCAA[A/G]GTAATTTACAGATTC | 9474 |
rs201789818 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196841 | CCTTAACCACACCCA[C/G]AAACTAGAAATTGGC | 9474 |
rs201797721 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243324 | CAAATTCTACTTTAT[C/T]TTACTTTTTTGTAAC | 9474 |
rs201822659 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229430 | AGAGAGAGAGAGAGA[C/G]AGAGAGGAGAGAGAG | 9474 |
rs201846002 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246398 | CTCTCTCTCTCACAC[A/T]CACACACACACACAC | 9474 |
rs201871870 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215262 | AAGTGAAATTCTGTT[-/C]TCTTGATGCCCAGTT | 9474 |
rs201888107 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106198113 | ACCCTTATAACAGAG[-/A]AAAATGAACTAAAAA | 9474 |
rs201910186 | in-del | -/C | 0.0460142 | 0.144533 | intron-variant | ATG5 | GRCh38.p7 | 6:106207531 | ACAGAGAGACCTCAT[-/C]CTCTTAAAAAAAAAA | 9474 |
rs201922125 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200494 | TTTTTTTTTTTTTTG[A/G]GACGGAGTCTCACTC | 9474 |
rs201935699 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201277 | TATTCAAGTGTATAT[A/G]TGTGTGTGTGTGTGT | 9474 |
rs202015782 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294693 | CAAAAAAAAAAAAAA[-/A]TTAGCTGGGCATGAT | 9474 |
rs202038204 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234113 | ATACTGGTATGTCTG[-/A]AGGGGGGTGGAGTTC | 9474 |
rs202054203 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307395 | AACTATTTTTTTTTT[-/T]ACATTCTTCTCTCTG | 9474 |
rs202076711 | in-del | -/AAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273611 | AAGGGGTAGAAAAGA[-/AAAG]AAAGAAAAGTCCAGC | 9474 |
rs202110655 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303975 | GGAAAAAAAAAAAAA[-/A]GAAGAAAAGAAATAA | 9474 |
rs202210597 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266035 | ACATGAAAAACCCTC[-/A]AAAAAAAAAAATCAA | 9474 |
rs267600752 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202053 | CTGCAGCCACAGGAC[A/G]AAACAGCTTCTGAAT | 9474 |
rs367544455 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314927 | AGTAACAAGATTGCC[A/G]AACTTCTCTAAAACT | 9474 |
rs367592243 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244926 | TCTCAAATACCAATG[C/T]CTAAGGAATTCACAG | 9474 |
rs367597588 | snp | A/G | | | intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106217493 | GCGTCCACTGTTTGC[A/G]AGCTTTTCCAGAACG | 9474 |
rs367609162 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106276388 | AGAATGGCGTGAACC[C/T]GGGAAGCGGAGCTTG | 9474 |
rs367619060 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251852 | ATTTTTTTGTTCCTT[C/T]TAAAAAGAGACAGAG | 9474 |
rs367633093 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235127 | GGCCTCCTCAGCCAA[C/T]GGATGCCCTGGATTC | 9474 |
rs367670654 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252002 | TGCATCATCACGCCC[A/G]GCTAATTTTTGTATT | 9474 |
rs367713820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106219852 | AGATTACACCCAAGA[C/T]AGACATATGGTCTAC | 9474 |
rs367751098 | snp | A/G | 3.81192e-05 | 0.00436556 | intron-variant | ATG5 | GRCh38.p7 | 6:106279615 | GGTTATGGCTGTATC[A/G]TATTTTATAAAGTGG | 9474 |
rs367765951 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | ATG5 | GRCh38.p7 | 6:106308506 | ACTGAAATGAAAATT[C/T]GTAAAACCGTATTTA | 9474 |
rs367819132 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242156 | CACACACACACACAC[A/T]TTTATAGAAGACAGG | 9474 |
rs367834021 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283283 | TTATCAGGTTTCAGT[-/T]ATCAGGGTTATTCTG | 9474 |
rs367842782 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323935 | TTTCCAGTCAAACTA[A/G]CTAGTATGCGCCTGC | 9474 |
rs367853722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267818 | TGGACCTATTCCTTA[C/T]ACCTTATACAAAAAT | 9474 |
rs367884599 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296051 | GCTGAATGCATAAAT[C/T]GAAGAAGTCCACAGA | 9474 |
rs367887341 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187173 | CTTTAGTTGTTTTCA[A/G]TAAAGCATTCAAGTA | 9474 |
rs367944432 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206648 | GAGGGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 9474 |
rs367974817 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246370 | TTCTCTCTCTGTCTC[-/TG]TCTCTCTCTCTCTCT | 9474 |
rs367997627 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251217 | ACATGTTGTTGATCA[A/C]CTGCATTCCAGGTTG | 9474 |
rs368112656 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207787 | AACAAAAGATGCCAG[C/T]CAGTTGTTAAAGAGT | 9474 |
rs368112819 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219098 | TTTCAAATTTTAAAC[A/G]AGCAGAATAAATTCT | 9474 |
rs368133943 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202591 | TAGGTACAATAAGGA[A/C]AATCCTTATTTTTAA | 9474 |
rs368147953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106230148 | TGATAGGGAGACTCT[C/T]GTGGAAGCAGAGTTA | 9474 |
rs368159136 | snp | C/G | 1.65201e-05 | 0.00287398 | intron-variant | ATG5 | GRCh38.p7 | 6:106293022 | GAGAAATGCAATTTA[C/G]TATACCTTAAAATGT | 9474 |
rs368161056 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318424 | TGCTGCTTCTGAGTC[C/T]CTTCCCAAAAGAGAT | 9474 |
rs368172390 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106206255 | CCCTTCTGCCATGTT[-/G]GGGGGGTGGGGGTGG | 9474 |
rs368194044 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247506 | AGTAAATTCTTGTGA[C/T]TTGCAGTAGTTCTGT | 9474 |
rs368226142 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | ATG5 | GRCh38.p7 | 6:106295096 | TACACACATATATAG[G/T]ACTATAGACAAGTTA | 9474 |
rs368257234 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106213803 | GAAAACTTATCTTTG[-/A]ACAATTGATGTGATA | 9474 |
rs368272824 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235422 | ATTCCGCAGGAAGCA[A/G]TTAGACTGGTCGTCA | 9474 |
rs368283358 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106224651 | GAGGCCTGGGTGGGC[A/G]GATCACCTGAGGTCA | 9474 |
rs368285069 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233140 | ACCTGTGGCTACAAG[A/G]TTTCCAAACCAAAGG | 9474 |
rs368290118 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219980 | CCAAGCAATATAACA[C/G]TGGTTCTCTGAACCA | 9474 |
rs368297491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255440 | AAAAACTACTGCTTG[A/G]AAATTTAAAGAAAAT | 9474 |
rs368529031 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235022 | GTTGTTATTATGTTA[A/G]TCAATCCTGAATTGT | 9474 |
rs368553438 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263275 | ACAAAGTGGCTGTGG[C/G]CAGAGTCCTTCTCTA | 9474 |
rs368582938 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281424 | ATAAAATCTCATATA[A/C]ACAGAATTGCAGTAT | 9474 |
rs368620644 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199779 | AATTGCTCCAAGATT[C/T]AATGATCGTAAATAA | 9474 |
rs368677033 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106224806 | GAATCGCTTGAACCC[A/G/T]GGAGGCGGAGGTTGC | 9474 |
rs368686168 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305265 | TTCTGCTATTATCTA[C/T]AACTAACTTTACTAT | 9474 |
rs368838890 | in-del | -/T/TTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307535 | TTGATTTCAATACCC[-/T/TTTT]TTTTTTTTTTTTTTT | 9474 |
rs368839379 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264613 | TAGGTTTCCTACAAG[A/G]GGAAGCCCATCAGAC | 9474 |
rs368845767 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205627 | TTGGTTACATATTAA[A/C]AAACAGAAATTCTTC | 9474 |
rs368921836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233891 | TTTCTATGAAGAATG[C/T]GGCTTCCCAGAAATA | 9474 |
rs368938305 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223858 | GGCTCTGCCATCAAA[C/T]AATAAGCTAAACAAT | 9474 |
rs368956379 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194221 | TGAGGTTTGGGAATT[A/G]GAGTTTTTTTTATTC | 9474 |
rs368979074 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106322735 | ACCACTCCCTTGAAG[A/T]TCTCTCACATGGTTT | 9474 |
rs368979932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106265605 | ACCACATAATTGAAA[A/G]TAAAACACTCCTCTG | 9474 |
rs368991803 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263132 | CAGCAGTCTAAAGTC[A/G]ACCTGGAATGATCAA | 9474 |
rs369004507 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106292500 | TTGGAATTCTATCTC[C/T]TAACCCTTCTCTTAA | 9474 |
rs369017352 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246432 | CACACACACACACAC[C/T]CTTTCTCTCTCTCTC | 9474 |
rs369028457 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314552 | CAACAGGGTGAGACT[C/G]TCTCAAAATAAATAA | 9474 |
rs369075106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106298476 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 9474 |
rs369077295 | in-del | -/CTAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208156 | CATGGACACAACTAC[-/CTAT]CTTTCCTGAACCTCA | 9474 |
rs369186423 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197152 | CTATAGTCAAGGATG[C/T]TATAAAAAAGGAAGT | 9474 |
rs369280550 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250268 | TATTTTTAAAAAATT[A/T]CTTCTTACACCCCTG | 9474 |
rs369306267 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244650 | GCAATCACAGTTCCA[A/G]TGTTATATTTGTATT | 9474 |
rs369417192 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191594 | GAATTCTAATCTCCA[A/G]TTACATGAAGGATTA | 9474 |
rs369443037 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210042 | TTTAAAGTTTGAGAA[A/G]CACTAGTCTACAACA | 9474 |
rs369480470 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276265 | GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAT | 9474 |
rs369501513 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300122 | TAAAATCTATGTAAG[C/T]CACATTTCAAAAATC | 9474 |
rs369519520 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199156 | CACTTTGGGAAAGCT[C/T]AGTAGTTTCTTTTAA | 9474 |
rs369630102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106248886 | GAGGTTGTGGTGAGC[C/T]GAGATCACGCCATTG | 9474 |
rs369630165 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289111 | ACCACAGAAGATAAA[G/T]GCAGAGACACCAAGT | 9474 |
rs369682504 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282138 | AAACATACAATGCAC[A/C]CATGTGCACACCTCC | 9474 |
rs369688158 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262870 | AGGAGATTCCCTCAT[A/G]TAGCCTACACCACCA | 9474 |
rs369736581 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | ATG5 | GRCh38.p7 | 6:106256038 | TATGCAATTGAGTTC[-/A]TTTTTACTTCACTCA | 9474 |
rs369783546 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319332 | GTAGTAATTATAGGT[A/T]TAAAAAAGCTAAAAA | 9474 |
rs369801979 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268430 | TTTACACTGTTGGTG[C/T]GAGTGTAAATTAGTT | 9474 |
rs369833045 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186532 | TGTTCAGGCAAATAG[G/T]TGATCCTTCAATCTG | 9474 |
rs369895764 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291362 | TACAGTGAGGTACAA[A/T]GCCCTGCTTTGTGCT | 9474 |
rs369917884 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261324 | GGTTAAGTTTGCAAT[A/G]AGAAGTTTACATAGT | 9474 |
rs369933147 | snp | C/T | 1.72627e-05 | 0.00293786 | intron-variant | ATG5 | GRCh38.p7 | 6:106279827 | TTCTGGAAAACTCTA[C/T]CAAAGGAAAAAATAT | 9474 |
rs369934343 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195162 | CAATGACCTAAAGCA[C/T]GTATTCATAAATACT | 9474 |
rs369949744 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308211 | AATATTTTCAATAAC[G/T]TATTCTAGTAATAGT | 9474 |
rs369959584 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290737 | TTTACACATGCATGA[C/T]CTTGTAACATCAAGC | 9474 |
rs369963709 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295057 | AAAATTAAAAAAAAA[A/T]ATACATACACACACA | 9474 |
rs370059690 | snp | C/T | 3.40368e-05 | 0.00412519 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279815 | CAGAAGGTCTTTTTC[C/T]GGAAAACTCTATCAA | 9474 |
rs370092827 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197844 | ATAGCAACACAAACA[G/T]ACTAACACAGCATCT | 9474 |
rs370123858 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212238 | TAGCATTAATTGAAC[C/T]GAAAAGGCATTTTAG | 9474 |
rs370129784 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296981 | ATCAGGACAAAATAC[A/G]AAGAGAGACAGCAGT | 9474 |
rs370173954 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280896 | ATCACTTCCTCCAAA[C/G]ACTTAAATATTTAAG | 9474 |
rs370247270 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291033 | CTAACAAATAACAAA[A/G]TCTCAACAACCACAG | 9474 |
rs370248988 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276257 | ATCACGAGGTCAGGA[G/T]ATCGAGACCATCCTG | 9474 |
rs370261002 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303151 | AAATTTTAAAAAGGA[C/G]AGAAAAATCCATGAA | 9474 |
rs370346237 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317286 | ATATTTCTCATCTTT[A/G]ATAGGCAGCTAATTC | 9474 |
rs370365812 | in-del | -/ACAAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286314 | CAAAGCACATGGGGC[-/ACAAA]TCACCTTGTTTGTTC | 9474 |
rs370376831 | in-del | -/AAAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273619 | GAAAAGAAAAGAAAG[-/AAAAG]TCCAGCTTAGAGAGA | 9474 |
rs370402321 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320625 | TCAAAAGGCTGTTCT[A/G]AAAAAAAAAAAAATC | 9474 |
rs370408715 | snp | A/G | 3.45292e-05 | 0.00415493 | intron-variant | ATG5 | GRCh38.p7 | 6:106248276 | TATTTGTTATTAAAA[A/G]TGAACAACATTATAA | 9474 |
rs370452838 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317282 | AATAATATTTCTCAT[C/T]TTTGATAGGCAGCTA | 9474 |
rs370465635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106227797 | TTCTGGTTATTGTCA[A/G]GCTATGAGCACAAAC | 9474 |
rs370498227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266899 | TAGTCAATATCATAC[A/G]GAATGGGCAAAAGCT | 9474 |
rs370501583 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257422 | CACAAATCTATGAGT[A/G]ATGCATTGTGCTATG | 9474 |
rs370505224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293383 | CCATGTGAACTGTTA[G/T]GTCACAGTACTGTTG | 9474 |
rs370558728 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316375 | CTTCAAAAAAAAAAA[-/A]CGATGATCACCAATC | 9474 |
rs370570627 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273618 | AGAAAAGAAAAGAAA[A/G]AAAAGTCCAGCTTAG | 9474 |
rs370573200 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223198 | CATAACTTTTGCTCT[C/T]ATCTTATGTTTTAAA | 9474 |
rs370608907 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222913 | TAAAGCGCAATAAAT[A/G]TTAGCTGCTATTATT | 9474 |
rs370666495 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200945 | GGTTCAAGGATCCCT[A/G]AGGATACCAAAATCC | 9474 |
rs370781924 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326353 | GGCCGAGGCGGGCGG[A/G]TCACGAGGTCAGGAG | 9474 |
rs370832051 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240400 | TTATAAAATAAAAAG[A/T]TAAGAAGAAAAGATA | 9474 |
rs370945021 | in-del | -/TTCT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214403 | TTGAAAATAAGCACT[-/TTCT]GTACTTATGTTGAGA | 9474 |
rs370945258 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229331 | GTTCCCCACCACCCT[C/T]GCCAGGGCCCCAAGT | 9474 |
rs370966331 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263884 | ACAAAGATGGAAAAA[A/G]AAAAAAAAACAGCAC | 9474 |
rs370977998 | snp | A/G | 1.66377e-05 | 0.00288419 | intron-variant | ATG5 | GRCh38.p7 | 6:106316069 | AAATGGACAAGGTTA[A/G]ATATCCCATTTGCCA | 9474 |
rs370986121 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251206 | ACAACCATGCCACAT[C/G]TTGTTGATCACCTGC | 9474 |
rs371020624 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234161 | AAACATGTAAAGGAA[A/G]TAACCTCCCAACTGA | 9474 |
rs371039974 | snp | C/T | 0.00072637 | 0.0190436 | intron-variant | ATG5 | GRCh38.p7 | 6:106248104 | GCTTCAATTAAGATG[C/T]CTGAGGCTTTCATAA | 9474 |
rs371051420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288076 | CCCAGGTTCAAGCGA[C/T]TCTCCTGCCTCAGCC | 9474 |
rs371058494 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247092 | TCTCTGAACACATAG[C/T]TATGTGATGGCTCTA | 9474 |
rs371107537 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218616 | CTTTGATGTGTAGAT[A/C/T]CTTTGAAAGCCACTC | 9474 |
rs371207293 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106215129 | CTGCATATGAACATG[C/T]TTTATCCTTTTGGTG | 9474 |
rs371284426 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207227 | CCCATCTCTCCTCTA[A/C]TCATGTGCCTTCACC | 9474 |
rs371287160 | in-del | -/CTTT | 0.0142736 | 0.0832652 | intron-variant | ATG5 | GRCh38.p7 | 6:106214401 | AGTTGAAAATAAGCA[-/CTTT]CTGTACTTATGTTGA | 9474 |
rs371306062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288890 | TGTTTGAAAACTGTT[G/T]AACAGTGTTTTTTTG | 9474 |
rs371307340 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260378 | ATGCTGTTTGGGATA[C/T]TTTTATATCCTTCTA | 9474 |
rs371344118 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239185 | AAAAGTTTGTAAAAA[C/T]ACAATAGGATGAGAT | 9474 |
rs371395712 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259283 | TGTTTTAAATGTATC[A/C]CATAACTTTTAGGGA | 9474 |
rs371428386 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106194643 | CCTGGGTTCAACCAA[C/T]TCTCCTGCCTCAGCC | 9474 |
rs371459366 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204721 | TGCTGGCTTGTGAAG[A/G]TGCCTGCTTCCCTTT | 9474 |
rs371461351 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216509 | AAAAGGCCATATATT[A/G]CATGATGCTAATTAC | 9474 |
rs371464219 | snp | A/C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285705 | AAGCAGTCATAGACA[A/C/G]TATGTATATGAATTT | 9474 |
rs371514215 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303731 | ATAAGATTTATTAAA[A/T]GTATACAAGGTTGGT | 9474 |
rs371554631 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238872 | AAAAGGGAAGGTCAA[C/T]GTTATGGAATGAAAA | 9474 |
rs371613147 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238174 | TTTAAAACTTTTATT[A/T]ACTTTTATTTTTTAG | 9474 |
rs371615534 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320040 | GATACACACAAGCCT[A/G]TATGTTCCCATTTTA | 9474 |
rs371654024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106208127 | AGTCCTGTTTCTGTC[A/G]TTTATTATGGAACCA | 9474 |
rs371782168 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256237 | AAAACACTATTAATC[G/T]GTTAATGATTATCCA | 9474 |
rs371797325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106268357 | CAGTTAGAATGGGGA[C/T]TATTAAAAAGTCAGG | 9474 |
rs371870047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299850 | TACTGCCCAAGTTCA[C/T]GTCACTAAAATAAAT | 9474 |
rs371877834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226035 | CCTAAACTCTCACCT[A/G]TGGGAAACCCTGAGG | 9474 |
rs371887325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203130 | CATTATTTCAACTTT[A/T]CGATAGGTTTCACAA | 9474 |
rs371896991 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215751 | GCAACCAAAGAAAAA[A/G]ACAGACAAACTGGAC | 9474 |
rs371900472 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261013 | ACCAGCATTAACTAC[A/T]GATTGTTGAGTTAAA | 9474 |
rs371919447 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285968 | GTAACTGCCTAGTAT[A/G]TAGCCAGATGTCTCT | 9474 |
rs371926984 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ATG5 | GRCh38.p7 | 6:106265574 | AGCACCACATAGCAT[G/T]TGTATTCTAAAATCG | 9474 |
rs371952787 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ATG5 | GRCh38.p7 | 6:106304650 | GATGGAAATCAGATC[A/G]GTAATTACTGTGAGT | 9474 |
rs371965689 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269733 | CACACCCACCCGGAA[A/C]TCCAGCTGGCCCGCA | 9474 |
rs371985126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285101 | TCTGTTTTTCCTCTA[C/T]ACCAATTTCCATCTC | 9474 |
rs372074617 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240649 | TAAACTAATACATTT[C/T]TGAAAAGTAAGCTGG | 9474 |
rs372083870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106295215 | TTTTAACGTCTTCAA[C/T]TTATTTTTTAGAATA | 9474 |
rs372102128 | snp | A/G | 3.34868e-05 | 0.00409173 | intron-variant | ATG5 | GRCh38.p7 | 6:106186688 | CCATCTATTCCAAGA[A/G]AGAAACCCAACAACA | 9474 |
rs372114639 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194092 | AATGAAAATAATCAG[A/C]ATTATTATTGCCCAA | 9474 |
rs372243825 | snp | A/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224930 | AGAAATACATCAATT[A/G/T]AAAAAGTGAGCTATT | 9474 |
rs372285770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189918 | CAAGTGAACTAGTTC[C/T]ATATGAACTTCTTTA | 9474 |
rs372290051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238226 | CCCAGGCTGGAGTAC[A/G]GTGGCATGATCTTGG | 9474 |
rs372307438 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196552 | ACATGGTGAAACCCC[-/C]GTCTCTACCAAATAT | 9474 |
rs372435644 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292050 | AGAAACTCAGACACC[C/T]AAATGACTTTTTCAA | 9474 |
rs372492610 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235418 | CCCAATTCCGCAGGA[A/T]GCAGTTAGACTGGTC | 9474 |
rs372540364 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260087 | ACAGGGCAGGGAACA[C/T]CACACACTGAGGCCT | 9474 |
rs372577686 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230398 | CTAGGACTCACCCCT[A/G]AGCACAAAGGCAATG | 9474 |
rs372585339 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221872 | ATATATTAGGCTAGC[A/G]TAATAAAAATATGAG | 9474 |
rs372586400 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319430 | CTGTGTGGCAGGTGC[C/T]AGAAGAAGAATAATG | 9474 |
rs372689401 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280621 | GAGACGACTGATGCA[C/T]TTTTCACTGAAAAAA | 9474 |
rs372727021 | in-del | -/GC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229575 | AAAAAAAAACAGTGT[-/GC]CCTATTCCTTTAAAA | 9474 |
rs372734301 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322710 | AAATGCCCCAGGACT[C/T]AGTCCTTGAACCACT | 9474 |
rs372813235 | snp | C/T | 6.0581e-05 | 0.00550335 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308462 | TTTGTCAGTTACCAA[C/T]GTCAAATAACTTACT | 9474 |
rs372846400 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197002 | TGTATCAAGGGAGAC[A/C]CCCCACTTATATAAA | 9474 |
rs372865239 | in-del | -/AACTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196958 | TAAAAAGCAACTGTT[-/AACTT]TAGTTTTTACAGATA | 9474 |
rs372895188 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268983 | GCAAACCACCATGGC[A/C]CATGCATACCTATGT | 9474 |
rs372910884 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184108 | TTTTTTATCCTTACA[C/T]AACTCAAATATTGCT | 9474 |
rs372950154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282784 | TATTCTGTGATTTAC[A/G]TGGATTGAGATTTTT | 9474 |
rs372958970 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185105 | TTGATTAAGCTTTAC[A/C]ATTTCCATTCCAGAA | 9474 |
rs373006259 | in-del | -/AGTTATT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250267 | TATTTTTAAAAAATT[-/AGTTATT]TCTTCTTACACCCCT | 9474 |
rs373028302 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298722 | AACATGCGGTTCAAT[A/G]CAAATTTTTATGTTA | 9474 |
rs373066310 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250269 | ATTTTTAAAAAATTT[C/G]TTCTTACACCCCTGT | 9474 |
rs373155211 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274527 | ATGAAATAAATGTGC[C/T]ATCTATTATGTCACA | 9474 |
rs373168444 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301435 | AATGTTAGCAGGTGT[A/G]GTAAAAAGAGCCCTG | 9474 |
rs373203077 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186073 | ATCTTTTACAAAAAA[C/T]TACTTGCAAGTTATT | 9474 |
rs373226934 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222325 | ACCCCATATACTACA[C/T]GCATGAGCATGGGAA | 9474 |
rs373246467 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214549 | AATTGATACTATGAT[C/T]AAATAAAAGCATCCA | 9474 |
rs373282654 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195713 | CATGGGGAGAAGTCT[C/G]TCACACAGATGTACT | 9474 |
rs373296763 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229570 | ATAGTAAAAAAAAAC[A/T]GTGTGCCCTATTCCT | 9474 |
rs373326246 | snp | A/C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248798 | ACAAAATTAGCCAGG[A/C/T]GTGGTGGTGCATGCC | 9474 |
rs373358721 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236391 | CATATGTTGAATTTT[C/G]AAAGAAACTGGTAAA | 9474 |
rs373363330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197161 | AGGATGTTATAAAAA[A/C]GGAAGTTTAAAACAA | 9474 |
rs373437300 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207713 | AAGAGTAACAGGCAC[A/G]ATCATCACAAACTTA | 9474 |
rs373449378 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226795 | AGTTACAAAAAAGTA[C/T]CAAACAAAAATTCTG | 9474 |
rs373506916 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211628 | GGCAGGAGAATCACT[C/T]GAACCTGGGAGGCAA | 9474 |
rs373509311 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205811 | CATAGTGTAGCTAAA[C/T]GCTGTAGAATGGTAA | 9474 |
rs373513992 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191875 | ATTTTTTTAGTACTA[A/G]ATATATCAAAAGATA | 9474 |
rs373527409 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106265882 | AGCACTAAATGCCCA[A/C]ATCAGAAAGCTCGAA | 9474 |
rs373561168 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242155 | ACACACACACACACA[C/T]ATTTATAGAAGACAG | 9474 |
rs373567186 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106261759 | TAGGGGTTTATTTTG[C/G]AGGTAGTATTGACAG | 9474 |
rs373605372 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228608 | CCCGCCACCATCTTC[A/G]GAGTTCTGGGAGCAA | 9474 |
rs373633196 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252231 | ATATATACTTCTCGC[A/C]AGAGCTACAAGCAAT | 9474 |
rs373690748 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241612 | GATGCTTCTATATAT[A/G]TGTTTTTTGGCTGAG | 9474 |
rs373748467 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196641 | AAGCACAAGATTGCT[C/T]GAACCTGGGAGGCAG | 9474 |
rs373794853 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316165 | AAACAAGTTGGAATT[C/T]GTCCAAACCACACAT | 9474 |
rs373808252 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242940 | ATCCTAACAAACATG[A/G]CCATAATTTGCCACA | 9474 |
rs373863554 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300676 | CATCATGTTACTACA[A/C]TGAATACTCTAGACA | 9474 |
rs373882027 | snp | C/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202026 | GATCTCCTAGTGTGT[C/G]CAACTGTCCATCTGC | 9474 |
rs373884268 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253307 | TGGGCCCAGTGGGCT[A/G]GCCTCTGCGTCAGGG | 9474 |
rs373885087 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106208654 | GGGAATACTAATAAA[C/T]AGACTTAATTAAAAT | 9474 |
rs373917490 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207830 | TGGGGGTGGTGGCTC[A/G]TGCCTGTAATTCCAG | 9474 |
rs373940020 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327443 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 9474 |
rs374004871 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187010 | CAAAATTTATTTTAG[A/T]TATACATTAAAAACT | 9474 |
rs374017834 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208993 | GATATCATTACACAC[C/G]TACCAAAATATCCAA | 9474 |
rs374034051 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231982 | TTAAAAAAGATTGTC[C/G]AAATAGAAATAAGCC | 9474 |
rs374063999 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305304 | TTTCTTTAAAAAATC[C/T]TTAAAACCAAGCATT | 9474 |
rs374113296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276187 | TTAAGAAACTGGGCC[A/G]GGCGCGGTGGCTCAC | 9474 |
rs374115522 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290948 | GTTGAAATTTTACCA[C/T]TGACAACAAATACTA | 9474 |
rs374120428 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227133 | AGAATAAAATCAAAG[A/C]GATCCACACCTAGGT | 9474 |
rs374146625 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273619 | GAAAAGAAAAGAAAG[A/G]AAAGTCCAGCTTAGA | 9474 |
rs374151644 | in-del | -/TGGG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286309 | CCGTTCCAAAGCACA[-/TGGG]GCTCACCTTGTTTGT | 9474 |
rs374184911 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325561 | CTCCTTCCGGCTCCC[-/C]GCACTGGTGGGGACG | 9474 |
rs374223584 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232927 | TTCAAACCCAATGTC[A/T]CAACTCACCTGGACT | 9474 |
rs374264661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106219021 | AAAAAGGAAGAAGGA[A/G]AGAAAAGAGAAAAGG | 9474 |
rs374287964 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106273315 | TTTTAGTAGTTTTTC[-/TA]TGTTACCACAGTTAT | 9474 |
rs374329630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106187597 | AAAATACAATGTCTA[A/C]ACCTCTCAGCTTCCT | 9474 |
rs374402837 | snp | A/C | 1.65493e-05 | 0.00287652 | intron-variant | ATG5 | GRCh38.p7 | 6:106202119 | AAAAAATGATTCAAG[A/C]AATTAAGTCTTTGTT | 9474 |
rs374436120 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261821 | GTTGAAAAAAATGAA[-/A]CAATTATTACCGGGG | 9474 |
rs374442938 | snp | C/T | 1.69743e-05 | 0.00291322 | intron-variant | ATG5 | GRCh38.p7 | 6:106186711 | CAACAACAATAAAAG[C/T]CAAAACAGTTGAAGA | 9474 |
rs374462326 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | ATG5 | GRCh38.p7 | 6:106309620 | GAAAAAGCAGTTTTT[-/C]CCCCCACAGGAAGTA | 9474 |
rs374464370 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277719 | CTCAGAAGGCTGAGA[A/C]ATGATAATCGCTTGA | 9474 |
rs374499948 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247992 | TCAAATATTTCAGTG[C/T]GGTATCTGACTTGAT | 9474 |
rs374505771 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195122 | TCCACAAGCAGCAGC[-/A]TCATCATTAGTTACT | 9474 |
rs374516139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238677 | CAGAGAGAAGACCAG[A/G]GAACAAAGAGACTTC | 9474 |
rs374591911 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273015 | TCATTCTACTATTTT[A/C]TTTGCTCTTATTTAT | 9474 |
rs374604026 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324300 | AGTTGTATTGCGCAT[G/T]ATAAATAATGCAGAG | 9474 |
rs374632380 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288024 | TGCCCAGGCTGGAGT[A/G]CAGTGGCATGGTCTC | 9474 |
rs374649148 | in-del | -/GG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251667 | GGAGGGAGGAAGGGA[-/GG]GGGAGGGGGAGAGAA | 9474 |
rs374650083 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311211 | TAGGCAATGAGGATA[C/T]AACATTGAAAGAGAC | 9474 |
rs374655232 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300534 | ATATGTTCCGAGAAA[C/T]GCATTGTTAAGCAAT | 9474 |
rs374657422 | in-del | -/TTTTA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242566 | TTTATGTTACATTTA[-/TTTTA]CCATGATTAAAAATT | 9474 |
rs374684524 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318145 | GAAAATATAATCCAA[A/G]ACAATTGCTCTTCCC | 9474 |
rs374689689 | snp | C/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325887 | AGGAGGCCCGAGTCG[C/G]TCTTGAGCATGCGCC | 9474 |
rs374698397 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196058 | AATGCTTTTCATTTA[C/T]GTGTCTGATGTTCAT | 9474 |
rs374706743 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238220 | CTGTAGCCCAGGCTG[C/G]AGTACAGTGGCATGA | 9474 |
rs374730056 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288409 | GAAAAGCTTGAAGAA[A/G]GTACCATTTTCATTG | 9474 |
rs374757627 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316374 | AAGATTATCCACTTC[-/A]AAAAAAAAAAAACGA | 9474 |
rs374761639 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106294363 | TGGGCACGATGCTTA[A/T]GGGATAGCCCTGCAC | 9474 |
rs374780578 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246430 | CACACACACACACAC[A/T]CCCTTTCTCTCTCTC | 9474 |
rs374796186 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216351 | GTGGAGACAATCCAC[A/G]TGTCTATCAATTGGT | 9474 |
rs374802934 | in-del | -/GA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293948 | ATGCTTGGGATTAGA[-/GA]AGTGTTTCAGATTTC | 9474 |
rs374818236 | snp | C/T | 1.6766e-05 | 0.00289529 | intron-variant | ATG5 | GRCh38.p7 | 6:106293128 | ATGAAACAGTATATT[C/T]TGAGAAAATAAATAT | 9474 |
rs374852935 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284728 | GTGGGGTTTTTTTTG[-/T]TTTTTTTTTTTTGCT | 9474 |
rs374883371 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249862 | TCCTTAATGACTATG[C/G]TGAGCATCTTCTCAT | 9474 |
rs374885387 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106226588 | CAGAACAATATTTCT[C/G]ATCCTTCAGAAGAAC | 9474 |
rs374910821 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301181 | AAGAAAGAGACTCTA[C/T]TTTGAGTTAGGCCAG | 9474 |
rs374976557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106198878 | CTGATAAAGAACTTG[C/T]ATCCAGAATATATAA | 9474 |
rs374983114 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284889 | TCCATATTCCGTATA[C/T]TAAACTGTTATTAGA | 9474 |
rs374985631 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218416 | TGAATCACAATATTT[-/T]AACGTGAACATTTTA | 9474 |
rs374999788 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184942 | TCTTGTGCAAAAATA[C/T]AAGTCAGTGGATTTT | 9474 |
rs375027044 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295712 | GGGACTACAGACATG[G/T]GCCACTATGCCCAGC | 9474 |
rs375092302 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310242 | GGCAGAGCCAACAAC[C/T]GTAATTTTAAAAGAA | 9474 |
rs375098135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212991 | TTTATTTCCTGTCCA[C/T]GTTTTAAAAAAGCTT | 9474 |
rs375122490 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106271821 | GGAAATAGAGAAGGG[G/T]ATCCTTGAAGAAAAA | 9474 |
rs375141924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106259279 | TTATTGTTTTAAATG[C/T]ATCCCATAACTTTTA | 9474 |
rs375171354 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282562 | TACACTGAGCAGACA[C/T]TCTTGCCTTTTTCCT | 9474 |
rs375174491 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214221 | TGTACACAATATACA[A/G]TACCTCATTAAATAA | 9474 |
rs375177407 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200522 | CTCTGTCACCAAGGC[C/T]GGAGTGCAGTGGCAT | 9474 |
rs375178629 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297493 | CAAGAAGGGCCAGAA[A/G]TAATAAACTAGAACC | 9474 |
rs375190951 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216910 | AAACAAATAAATAAA[G/T]AAAAGGGTGACCTCT | 9474 |
rs375215126 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268689 | TACCATGGAATACTA[C/T]GCAGCCATAAAAAAG | 9474 |
rs375303498 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251902 | CTGGAGTGCAGTGGC[A/G]AGATCTCTGCTCACT | 9474 |
rs375358794 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106319932 | GTAAGCAGGTGAGAT[C/T]AGATAATAAAAATTA | 9474 |
rs375386210 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285685 | ACTAGGCTGTTGTAG[A/C]CGCAAAGCAGTCATA | 9474 |
rs375395184 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310154 | ATTTCCACTGCCCAA[A/T]ATAGTGCCTGCTTTA | 9474 |
rs375408346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321601 | CTGACCTCATGATCC[A/G]CCTGCCTCGGCCTCC | 9474 |
rs375430418 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235595 | AACTTAGCTCACACC[C/T]GACCAATCAGGTAGT | 9474 |
rs375491389 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315630 | GTGTATGTGTGCATG[C/T]TTATATGTTCTTTAA | 9474 |
rs375539564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106214516 | AGGGACACTTAATCT[C/T]CAAAGGAGAAGTTTC | 9474 |
rs375599693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258861 | ATAGTAATTCAACAA[A/T]TCTCATCTCCTGTAG | 9474 |
rs375665956 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106233838 | TCACTGCACCCCCTC[A/C/T]ATGCTGCTGTACAAC | 9474 |
rs375796282 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317991 | ACTGAGATTCACCTT[A/T]TGATGATGAAGAGAA | 9474 |
rs375807691 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211443 | AGGCCGGGCGTGGTG[G/T]CTCACGCCTGTAATC | 9474 |
rs375823387 | in-del | -/AGC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282868 | ACACCTTATTGCAGC[-/AGC]CTCAACCTCTGGGGC | 9474 |
rs375891279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269710 | CCGAGTGCGGGGTCC[A/G]CCAAGCCCACACCCA | 9474 |
rs375897501 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | ATG5 | GRCh38.p7 | 6:106269942 | GCAAGGGCTGTGAGG[A/G/T]CTGCCAGCACGCTGT | 9474 |
rs375903296 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106319653 | TTCAGGCAGAACTCG[A/C/T]CTTGTTTTCTCTTGG | 9474 |
rs375926512 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106309589 | AAAGAAAAAGGAATT[C/T]TTACTATTTAATATA | 9474 |
rs375930814 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258202 | GGTAGATCCCGTCTC[-/C]TAACAAAAAAAAAAA | 9474 |
rs375932973 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299316 | AATAGTTGTTATACC[A/G]TATTGGACTTTTTGT | 9474 |
rs375947890 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296850 | AAGCAGACTCCATTC[C/T]GGAATCAGTTTTTAG | 9474 |
rs375967350 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254887 | ATTCTATGTGAATGT[A/T]GCCTGTTGGAGTTAT | 9474 |
rs375978983 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247509 | AAATTCTTGTGATTT[A/G]CAGTAGTTCTGTTCT | 9474 |
rs375980610 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288087 | GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGAAGC | 9474 |
rs375996038 | in-del | -/ATGT | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185875 | AAAGTGATCTACTGT[-/ATGT]GAGTCAGAAAGTACT | 9474 |
rs375997375 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317793 | AACTCACTGAAAATA[C/G]GAAAGACCTCACTAC | 9474 |
rs375997620 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250577 | CCTCTCACATATGAA[A/G]CAATTATTCTGTCAA | 9474 |
rs376017669 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209661 | AACTAAATACACACA[C/T]ACAGTATATGTAAAA | 9474 |
rs376032727 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184465 | TGTTTTAAATAAAGA[C/T]GGACACAACATTTAT | 9474 |
rs376065697 | in-del | -/ACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322220 | AGGTGCCCACCAACA[-/ACA]TCTGTTAACCAATCA | 9474 |
rs376065896 | snp | A/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299135 | GTCCACCCTTGGTAC[A/G/T]TGTGGGGATTGGTTC | 9474 |
rs376136016 | in-del | -/GAGATAGAAAAAACAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257849 | GTTTAATTAAAACAG[-/GAGATAGAAAAAACAG]CATGCTCAAACAAGT | 9474 |
rs376181818 | snp | C/T | 0.00595198 | 0.054227 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186500 | ATGCTCTGATAAATC[C/T]CATTTAAGGATGATT | 9474 |
rs376185430 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246227 | CTGCCCAAGTGCCTT[A/G]ACACATTAAAGATCA | 9474 |
rs376229167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261627 | AGTGGTCACTGCTAC[C/T]TTAAATGAGAAGCAG | 9474 |
rs376248259 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304317 | AAAATAAAGGAACAT[A/T]CAGAAAACAAAATTA | 9474 |
rs376331507 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230517 | GCTACATCAGTGAGC[A/G]TAACTAATCCGATAA | 9474 |
rs376346678 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245640 | TGTCTCTCTCTCTCC[A/G]GTTATGCAGAAATTC | 9474 |
rs376439641 | snp | C/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325838 | GACCCCACGTGGTCC[C/G]AACTCCGCCCTCCGT | 9474 |
rs376465661 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248515 | AAACATACGACTACT[C/T]GTGTTATCAAGGCAA | 9474 |
rs376493675 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant | ATG5 | GRCh38.p7 | 6:106316062 | CTTACAAAAATGGAC[A/G]AGGTTAAATATCCCA | 9474 |
rs376531592 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236323 | GTTTTCTCGGACATA[C/T]ATTTTCATTTTTCTT | 9474 |
rs376552569 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282408 | AGGTTCCTGTTTTTT[A/T]ATCAGTGTAAGTTTG | 9474 |
rs376583384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316490 | TCAAAATTACATATG[C/T]CAGTAATATTCATTG | 9474 |
rs376589405 | snp | A/C | 1.64846e-05 | 0.0028709 | synonymous-codon, missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202048 | TCCATCTGCAGCCAC[A/C]GGACGAAACAGCTTC | 9474 |
rs376597646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106253104 | TTAATTTCTTCATAC[A/G]TAATATGTTAAACAT | 9474 |
rs376621942 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211977 | TTACAAGGGTTGCTT[A/C]AGTGTATCACAGGAT | 9474 |
rs376622531 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296910 | TTTCTCATTTTCTAC[C/T]AACAATGGCAGAGAA | 9474 |
rs376625312 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277280 | GTTTTCTTCTGTTTT[A/T]TTCTAGTCATTGCCA | 9474 |
rs376668648 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195088 | GAAAGGAACACACAA[A/G]AGAGCTCATCATTAG | 9474 |
rs376670140 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240859 | ATGCAGCCATTAAAA[-/AA]GAATAAATTAGGCTG | 9474 |
rs376710406 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265747 | GCTCCTAAATAACTA[A/C]TTGGTAAATAACGAA | 9474 |
rs376763645 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314344 | GGCAGATCACTTAAG[G/T]TCAGGAGTTTGAGAC | 9474 |
rs376815915 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262920 | CAAAACTGGGCAGCC[A/G]TTTGGGCAGACACCG | 9474 |
rs376815930 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106295396 | CTCCGCTAGGCAAAA[C/T]AGTCTAATCTATTAG | 9474 |
rs376818623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307777 | CTGGCCCCAGGTGAT[C/G]CGCCAGCCTCGGCCT | 9474 |
rs376835180 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220015 | TGACCCTCCTTTAAA[C/T]TGATAGCCTTTTTTT | 9474 |
rs376873603 | snp | C/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198465 | CACCAAAATTAAATG[C/G/T]TTTTATCCTTCAAAA | 9474 |
rs376933544 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225012 | AAGCCATCATCATTG[C/T]TGTTAAAATAACTCA | 9474 |
rs376979420 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222498 | ATTATGTTTTTACTT[C/T]CTGTGCATGCACTTT | 9474 |
rs376999465 | snp | C/T | 1.65119e-05 | 0.00287327 | missense, synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106248224 | GTTTCCGATTGATGG[C/T]CCAAAACTGGTCAAA | 9474 |
rs377031147 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184019 | CTCCCCAAACTGAAA[C/T]GAAGAATAAACACTC | 9474 |
rs377035108 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234545 | GTAACTCCTCCCACA[C/T]GAATAGTCTGCCTAC | 9474 |
rs377039725 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234116 | ACTGGTATGTCTGAG[C/G]GGGGTGGAGTTCAAG | 9474 |
rs377112285 | in-del | -/ACT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310504 | CAGACTATATATACT[-/ACT]CATTGTTTTTCTTAG | 9474 |
rs377165342 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198788 | CTGGGAAAAAAAAAA[A/G]AGAGAGAGTGAGAAA | 9474 |
rs377201454 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219417 | ACAGTCAGCCCTCCC[C/T]ATCCAGGGGTTCTGC | 9474 |
rs377341368 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269602 | CAGCGCCGGTGGGCC[A/G]TCACTGCTGGGGGAC | 9474 |
rs377420577 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229039 | GCGCTCCTACCTTCC[C/T]TTCTGTCCCACACCT | 9474 |
rs377465913 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284172 | TGCATATCAGAATTA[-/A]CATATTCAGTTCTCT | 9474 |
rs377479410 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194630 | GCAACCTCTGGCTCC[G/T]GGGTTCAACCAATTC | 9474 |
rs377479461 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213558 | AATAGAGAAAGAGAT[A/G]AAGTCATTTGAGTAT | 9474 |
rs377538270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106242200 | GTCAAGGCTGGTCTC[A/G]AACTCCTGGGCTCAA | 9474 |
rs377550404 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263297 | CCTTCTCTAGATTCC[A/T]CCTCATTGGGCAGGG | 9474 |
rs377572131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106222152 | TGCTAGGATTACATG[C/T]GTGAGCCACTGCGTC | 9474 |
rs377577415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200575 | CGCCTTGTGGGTTCA[C/T]GTCATTCTCCTACCT | 9474 |
rs377603167 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106276707 | GAACACCTACTTAAC[-/T]GTCTAATTAAATTAT | 9474 |
rs377638769 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218377 | AAATCATAGTTAAAT[G/T]AAATCTTCCTTACTA | 9474 |
rs377704575 | in-del | -/AG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229415 | GAGACAGACAGAGAC[-/AG]AGAGAGAGAGAGACA | 9474 |
rs377722544 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271274 | TGGACTGAATGTTTA[C/T]ATCCCCCTATAATTC | 9474 |
rs386704565 | in-del | AGAAAT/TCCCACTCTAGGCACTCCTTAACCACACCCACAAAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196810 | ACCCAACTAATTTCT[lengthTooLong]TAGAAATTGGCAACC | 9474 |
rs386704567 | multinucleotide-polymorphism | CC/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205693 | TTATATATCTTTTTT[CC/TT]CACCCTTTCCCAAAT | 9474 |
rs386704568 | multinucleotide-polymorphism | CCC/TCT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207533 | CAGAGAGACCTCATC[CCC/TCT]TAAAAAAAAAAGAAA | 9474 |
rs386704569 | multinucleotide-polymorphism | CAA/GAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222212 | ATTTATTTGTGGAGA[CAA/GAG]GTAAAGAAAACTCAT | 9474 |
rs386704570 | multinucleotide-polymorphism | CTG/TTA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228118 | TAAACTATTTGGTTA[CTG/TTA]GAAAATAGCTTTATT | 9474 |
rs386704571 | multinucleotide-polymorphism | AA/GC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264012 | ATGAATTGACAGAAG[AA/GC]GGCTTCAGAAGGTGG | 9474 |
rs386704572 | in-del | CAA/TATTGG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264908 | CCAAAATATAAAGAC[CAA/TATTGG]CACTATGAAAAAACT | 9474 |
rs397763346 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235823 | ACTGCAAAAAAAAAA[-/A]TAGCTTAATTGAAGA | 9474 |
rs397829978 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279483 | ATCCATGAACAGAGG[-/G]ACACCAAAAGAGCAG | 9474 |
rs397841554 | in-del | -/TAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313768 | CAGCAAGGGACATAT[-/TAT]CTGAACTACAGCTAT | 9474 |
rs397941549 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198110 | AACACCCTTATAACA[-/CA]GAGAAAATGAACTAA | 9474 |
rs397956107 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200900 | ACACACACACACACA[-/CA]ATGTGGTCACTTGGT | 9474 |
rs397971332 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305107 | AAAAAAAAAAAAAAA[-/A]GATGAATTTTATTCC | 9474 |
rs397978595 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269404 | CCCGCGCCGTGCCCC[-/C]GCACTCCTCAGCCCT | 9474 |
rs398002515 | in-del | -/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106195832 | TGACTTCCCTTGTGG[-/T]TTTTTTTTTTTTTTT | 9474 |
rs398048729 | in-del | -/T | 0.5 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106295581 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTAC | 9474 |
rs398066134 | in-del | -/CTCT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235781 | TTGTATGGGAGCTCT[-/CTCT]GTCTTCACTCTATTA | 9474 |
rs398066135 | in-del | -/AAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308047 | GAAATAAAATTGAAT[-/AAT]GTCAAGAGATGACTT | 9474 |
rs398085204 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242636 | ACAACAACAAAAAAA[-/A]ACACCTCAAGCAACT | 9474 |
rs398110519 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217868 | GCTGATACATCCCAA[-/A]CAGTATTTCAGATTG | 9474 |
rs398110520 | in-del | -/GA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227576 | CTCTTGCAGTGGAGA[-/GA]CCCTGTCTCTATAAA | 9474 |
rs398110521 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242637 | CAACAACAAAAAAAA[-/A]CACCTCAAGCAACTT | 9474 |
rs398110522 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320638 | TGAAAAAAAAAAAAA[-/A]TCCATAAAGTGTTTG | 9474 |
rs527262485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201897 | AAATAACCTGTTGTT[G/T]ATAAATGTGGAATGC | 9474 |
rs527279626 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302537 | CACTAAAACAATCCA[C/T]GTGAGAAATCAGATG | 9474 |
rs527279892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300277 | ATTTTAATCTCCTGC[A/G]TAAATGGGTTAAGTT | 9474 |
rs527280516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106293406 | TACTGTTGCATCTAA[C/T]TGTCATCCCTGTATT | 9474 |
rs527289891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201050 | TTCATCTCTAGATTA[C/T]TTGTAATATTTAATG | 9474 |
rs527315956 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274483 | TTAAACTGTTGTTTA[G/T]CTGTTATAATCTACA | 9474 |
rs527316164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293912 | AATTAAATAATACAG[A/G]TTGAGTATCCCATTT | 9474 |
rs527326312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243033 | CTAAAATTTGGCTCC[C/T]TCTTCAGTTTAGAAG | 9474 |
rs527328007 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240668 | AAAGTAAGCTGGCAA[-/T]TTTTTTTTTAATCTC | 9474 |
rs527337604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250849 | TGACTCTCTTCTCCA[A/G]ATTCACCCTTCAATA | 9474 |
rs527354753 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325633 | CGCCTGACACACTGT[C/T]CTGCGGGGACGCGGT | 9474 |
rs527360720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250027 | CACATATTTTCTCCC[A/G]TTCTGTACATTGTTT | 9474 |
rs527441892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187572 | GGTTTGTCTCCTTTA[A/C]CTTCTCTTCAAAATA | 9474 |
rs527445076 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252090 | AAGTGATCCATCTGC[C/T]TTGGCCTCCCAAAGT | 9474 |
rs527447550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322804 | CTTCTGTCCAGACTT[C/T]TCTTTTGAACTGGCT | 9474 |
rs527460147 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288437 | TTGTTTTGGTAAACA[A/C]AACATACATCCAAAT | 9474 |
rs527461657 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239565 | TGCTCCAACAGATAT[C/T]AGAACGCTAAAATTA | 9474 |
rs527492563 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106301083 | AACAAATATAAAATG[-/T]GAACACCAGTTGTGG | 9474 |
rs527495896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323070 | ACTACAAGCGCTTGC[C/T]ACCAGGCTCGGGTTT | 9474 |
rs527549929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106235734 | CCAGGCATTCAAGCC[A/G]GCAACGGCTACCTTC | 9474 |
rs527589573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243767 | ACCCAAGAGGCGGAG[G/T]TTTCAGTGAGCCGAG | 9474 |
rs527596554 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276970 | TTGCAAAGCTTATAA[C/G]CTAGTTGAGAAATGC | 9474 |
rs527599241 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248799 | CAAAATTAGCCAGGC[A/G]TGGTGGTGCATGCCT | 9474 |
rs527616405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287384 | CAAAACAGGATTTGC[C/G]TGCTGTGCTTGAAAG | 9474 |
rs527623788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194293 | GGCAGTGCCATCACA[A/C]TGACAAATGTGATTA | 9474 |
rs527624571 | in-del | -/A | 0.288646 | 0.246995 | intron-variant | ATG5 | GRCh38.p7 | 6:106294679 | TCTACCCAAAAATAC[-/A]AAAAAAAAAAAAAAT | 9474 |
rs527643152 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184972 | TTTATCCTTACATAA[A/C]TCAAATATTGCTATT | 9474 |
rs527654147 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202232 | CATCACAGATGTGGT[A/G]TCACTGTGAAAAATG | 9474 |
rs527681879 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106228758 | TGGAGGAAAATACTG[C/G]GCACCTGTCGGCCGG | 9474 |
rs527696219 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296588 | TTTGGGAGGCTGAGG[C/T]GGGTGGTTCACCTGA | 9474 |
rs527714144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234502 | TAGCAATACTGTAGA[C/T]ACAACCAACTCCCAA | 9474 |
rs527746819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241879 | GAAGAGCTGCCAAAA[C/T]CAGGAAAGCCAATTC | 9474 |
rs527782019 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184161 | ATGGCAATTAGAGTT[C/G]AATTCCATGGTCATA | 9474 |
rs527782092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192741 | ATGTGTAATACTGAA[A/G]GTAAAATTTCTGAAA | 9474 |
rs527783962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285704 | AAAGCAGTCATAGAC[A/G]ATATGTATATGAATT | 9474 |
rs527787732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249333 | CCAGACATTTCATAT[A/T]AATGAAGTAATATAA | 9474 |
rs527819307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191861 | ATAAGAATAAGTTCA[C/T]TTTTTTAGTACTAGA | 9474 |
rs527832457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264109 | TGATAAAAGGTTATA[A/G]GAAATGCTAACTAGA | 9474 |
rs527875685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214744 | CTTTGACTGAATAAC[A/G]TGTGGTACAGAGAAG | 9474 |
rs527875806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311142 | TTTCTAGGACAAAAA[C/T]AGAAGTAAAACATAC | 9474 |
rs527887747 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281203 | CAATAAACTTTTTTA[A/G]AAGTCAAACTTATGA | 9474 |
rs527903419 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106222666 | AATGAACTTAATATA[A/T]GAAAGGTAATAATGA | 9474 |
rs527912489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214052 | AAAAAGAAAACAGGG[G/T]TTTACACAGGATATG | 9474 |
rs527940122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106229322 | GTGGGACCTGTTCCC[C/T]ACCACCCTTGCCAGG | 9474 |
rs527944972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222071 | TAATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 9474 |
rs527951757 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293402 | ACAGTACTGTTGCAT[A/C]TAATTGTCATCCCTG | 9474 |
rs528001730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269970 | TGTCACCTCTCATTA[C/G]TATAATCTGTATTGC | 9474 |
rs528003263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278673 | AACATTATCAGTTTG[C/T]TTCTTTGTTGGATTT | 9474 |
rs528027692 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231380 | ATCTCAGTCAGGTCA[A/G]TGATAGGTCGACAAC | 9474 |
rs528034710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314008 | ATGACTGTATAAGAG[A/G]TTTCTCTGGGTGAAG | 9474 |
rs528037245 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106274201 | CTTATAAGAAAAACA[A/C]CTTGATATTAAATAG | 9474 |
rs528041694 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260512 | AAGCACTTTGAAGAC[A/G]ATAATCAGGACTAAA | 9474 |
rs528097496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317913 | TCTAAAATTGAATCT[A/G]ATATAAAGGTGGTAT | 9474 |
rs528106372 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106231932 | AAATCAAATGCCTAA[C/T]AGGGTTTGCTTCCAG | 9474 |
rs528128203 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233532 | GTCCTTACACAGGTC[A/G]ATGAGCTTGCAACCC | 9474 |
rs528131967 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268877 | CACACGGGGGCCTGT[C/T]GGTGGGTTGGGGGCA | 9474 |
rs528144430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231285 | ATGGAGAGATATAAT[C/G]TTACTGCTAAATCAG | 9474 |
rs528162287 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106190631 | TCCACAAAGCACTTT[C/T]AGAAACCAGCATCTA | 9474 |
rs528179603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237636 | AAAAATCACTCTACA[C/T]CCCATAATACTTTGT | 9474 |
rs528185158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189318 | AAAACCAATAAAAGA[A/C]AACAGGCCAGGTGTG | 9474 |
rs528188545 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257938 | CTTGCTCCCATTATG[C/T]ACTTAATTGAGTAAC | 9474 |
rs528194654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106246067 | TAATTTTTATATTCA[C/T]TTTCATATCTCACTT | 9474 |
rs528228979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188590 | ATCTGAAAGGCAAAA[C/G]ACCAACCATGTTACA | 9474 |
rs528230841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289949 | GATATGTAGTTTAAA[A/C]GAAGTATTTTAATAG | 9474 |
rs528231037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281819 | AGAGTTCTGGTTACT[C/T]CGTGTCCTCAAACTT | 9474 |
rs528291018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106304280 | CGCTCCACAGTAAAA[C/T]TTTTTTAAATTATAA | 9474 |
rs528310518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219454 | AGATTCAACTAACCA[C/T]GGGTCGAAAATGTTT | 9474 |
rs528315352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210927 | CTCTACTGAATTCTA[A/G]TATGTATTCTGTATT | 9474 |
rs528345198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226421 | CATGCAAAGAAACAA[A/G]TATAAGCCACAAACT | 9474 |
rs528373941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267587 | CTACCTGACTTCAAA[C/T]TATATTACAAGGCCA | 9474 |
rs528399679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267193 | AAGCATTCCTATACA[C/T]CAACAGCAAAGAAGC | 9474 |
rs528411333 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106274963 | GTTGAAAGCATTAAC[A/C]GTTCTGCCTCCACTT | 9474 |
rs528437010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106318352 | GCTCTTTCTTTCCAT[A/G]ACATTCTCTTCTGTT | 9474 |
rs528448256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316697 | TTTTCCTACTCCAGA[G/T]AGTTTCTCCTCTCTT | 9474 |
rs528475727 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226264 | ATAAAAACCTGAAAG[A/T]ATTAGTTCAGGAAAG | 9474 |
rs528486180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216865 | CATACACACCAGCCT[C/G]GGCAACACAGACCAT | 9474 |
rs528524534 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250940 | ATTTCTCAGCAGAAA[A/G]TGCTAAAAGAAGTTG | 9474 |
rs528536012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224353 | CCATGAGCTAAATCA[C/G]TGCAAATGGCAAGAA | 9474 |
rs528541683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258900 | GATGACAGAACAGCA[C/G]AGCTAGCAGTAGCTG | 9474 |
rs528645887 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239468 | GGACACTATGGGGAA[C/T]TGAATAAGTGATTTT | 9474 |
rs528651481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106195508 | AATGACAATTTTTTT[A/T]AATACGTAATAAAAA | 9474 |
rs528669364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106289049 | GTAAAAGAAATTCTA[A/G]GAAGTCTGGTTAAAA | 9474 |
rs528669711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295547 | TCTTAAAGCAATCTA[C/T]AATATAAAATCAAGT | 9474 |
rs528672522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203592 | AAGAACAGAGAAATG[C/T]CATACATACATATTT | 9474 |
rs528697748 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234288 | ATACCACCCTCACTG[C/G]GCTCCATGAGGTCTC | 9474 |
rs528730340 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215667 | ATTCTTTAAAAAAAA[C/T]ATAAGAGGAAACCTT | 9474 |
rs528830387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203006 | AGAGAGACAGAGAGA[G/T]AGAGAAAGAGAGAGA | 9474 |
rs528847357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106188562 | TAAACAATCCACTGA[C/T]GATGCACAGTGTATC | 9474 |
rs528847812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281605 | TGGGATTGTTTCTAG[A/T]TACTGGCTATTATTT | 9474 |
rs528883734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237476 | CTTGTTCCATTGCTT[A/G]CCGGCTGGCTGTCCT | 9474 |
rs528897866 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229453 | AGAGAGAGAGAGACA[C/G]GGAGGACAGGGAGAG | 9474 |
rs528946843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236629 | TTATTAGCCATTCCT[A/G]TATCTTTTGTGAAAT | 9474 |
rs528986696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252444 | AAGCTTTTATATTGG[G/T]CTTGCAAATTTTAAA | 9474 |
rs528991589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106187831 | TCCTGTTAGAGGCAG[C/T]ACAGTCCCAGGTGAC | 9474 |
rs528991665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195431 | GTGAACTGAACCAGG[C/G]AGTAAACAGTTTTTT | 9474 |
rs528997014 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280404 | CAAATCTAAATATCA[A/T]CAGGTAAATGAACAT | 9474 |
rs529004655 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106267124 | AAAAACTCCTTAAGC[G/T]GTTAATAAACTTCAG | 9474 |
rs529013918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203456 | TGCCAACCACAGAGT[A/G]AATAAATAAATGTTA | 9474 |
rs529022100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288145 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 9474 |
rs529077246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317808 | GGAAAGACCTCACTA[C/T]GTCCTGATTACATTA | 9474 |
rs529085199 | snp | A/C | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106218511 | AAAAAGGACTAAAAA[A/C]TCTAATAATGGTTGG | 9474 |
rs529092133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311076 | ATAATTTTAATTCTT[C/T]ATGCCAAGTCCAATT | 9474 |
rs529123520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217943 | TATTTTCCACAATGG[A/G]AGTTTTAAAATAGTA | 9474 |
rs529214163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282337 | CCATATTTATTGTAG[C/T]ATTTATGCATTTCTC | 9474 |
rs529221533 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106323034 | ATGCCATTCTCCTGC[C/T]TCAGCCTCCCAGTGG | 9474 |
rs529225730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224325 | AAAATAGTTCATCTA[C/G]AAGATAAAGGACCCA | 9474 |
rs529227852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215976 | TCCTAAGAAATACGA[A/G]TGGCTAGTTAAATGC | 9474 |
rs529243171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264971 | GTATCATGATGGCAG[A/G]ATCAAATTCACACAT | 9474 |
rs529245603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324045 | CTATGGCCACCACTC[A/C]CATCTCTTGGCATTC | 9474 |
rs529246387 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314405 | CTACTAAAAATCTAA[A/G]AATTAACCGAGCATG | 9474 |
rs529259474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315484 | CAGAAGACATTTGAA[A/G]AGTGTTTGTAAAATA | 9474 |
rs529266288 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106245474 | TGGATTCTAGTTCTT[-/C]CATTTTTCATTTGTT | 9474 |
rs529298038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308562 | TACTAAGTAGGTTTT[C/T]GAATTTTAAGGAAAA | 9474 |
rs529299036 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288005 | TAGATGGAGTCTACT[C/T]TGTTGCCCAGGCTGG | 9474 |
rs529319102 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106197774 | CCAGGCAGTAGAGCT[A/G]TGAGTTAAATAAACC | 9474 |
rs529320757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230039 | TTACCATACAAAGGT[A/C]CGACCAGACCTAGGA | 9474 |
rs529399385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271671 | ATAACCAATGAGGTT[C/T]ATCCAAGACATGATA | 9474 |
rs529433163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106202953 | CAGGCGTGAGCCAAC[C/T]GCTCCTGGCCCCAAA | 9474 |
rs529467219 | in-del | -/TC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208308 | ACCTACATTATAGTT[-/TC]TGAGATAATAAAATG | 9474 |
rs529500792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251786 | AAAAGAAAAGGAGGA[G/T]AGAAAATCAGTGTTG | 9474 |
rs529562200 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216260 | AAGTATCTACCCAAG[A/C]GAAATGAAAATATAT | 9474 |
rs529576052 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106261190 | TACACAGAACACACA[-/T]TATTTCAAAAAATGT | 9474 |
rs529606564 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106309242 | TTATAACCGCATCAT[C/T]TTTCATGCTTTTTAT | 9474 |
rs529619291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319754 | CTGTAATAGATTCCG[C/T]TAGGGAGAAGGATCA | 9474 |
rs529628819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106212416 | GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTCA | 9474 |
rs529631542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265568 | CTTCTCAGCACCACA[C/T]AGCATGTGTATTCTA | 9474 |
rs529633213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208800 | CTTGTGTCTATAATA[C/T]ATAAGAACTCCCAAA | 9474 |
rs529664451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269197 | CTAGTTACAGAGTGT[C/T]GATTGGTGCATTCAC | 9474 |
rs529668306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262207 | CCTCCTGAGTAGCTC[A/G]GATTAGAGGCGTGTG | 9474 |
rs529680762 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215394 | GGGTTCTGTGGTGAA[C/T]GCTAAAGTTTATAAC | 9474 |
rs529694476 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187762 | ATGATGTATGGTGAT[A/G]ATGACTTGGCTGGCA | 9474 |
rs529708542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313046 | TGAAGGAGCCAGCAG[A/G]TAAGAAGTTGAAAGT | 9474 |
rs529755717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227245 | ATAACAAATTTCTCA[C/T]CAGAAATGATGTTGT | 9474 |
rs529777735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319158 | AAGAATTAAATGAAT[A/T]CATGTAAAGCACTTG | 9474 |
rs529794917 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211608 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 9474 |
rs529825083 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106276207 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 9474 |
rs529854837 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280219 | CAGACACCTACCATC[G/T]GACCCAGCCATTCCA | 9474 |
rs529890780 | snp | A/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317582 | TTCTGGTTATTAAAC[A/T]GAGTCCAGTGCTCTT | 9474 |
rs529904350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298354 | CATATTAAGAATTAG[A/G]AGATAAATTTAAACA | 9474 |
rs529904410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294311 | ACTCTGACCAAGATT[A/C]AAATATCAGTTAATA | 9474 |
rs529905299 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235420 | CAATTCCGCAGGAAG[C/G]AGTTAGACTGGTCGT | 9474 |
rs529907973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206753 | GCTCCCATAGAGAGA[C/T]CATGCATTCAAGTAC | 9474 |
rs529912540 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322629 | GATTCTCAAGAGGAA[C/T]TTTACTCAACAGTCC | 9474 |
rs529915154 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106220023 | TTTAAATTGATAGCC[-/T]TTTTTTTAAAAAGCT | 9474 |
rs529939374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299027 | TACCCTAAGTAAATC[A/G]TAACGTAACCATTGG | 9474 |
rs529940696 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106248903 | AGATCACGCCATTGC[A/T]CTCCAGCCTGGGCAA | 9474 |
rs529943632 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297512 | TAAACTAGAACCTCT[-/CA]GAGGTATATTTGAAT | 9474 |
rs529950835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305989 | CTAAAGGAAAAGATG[C/T]ATCAAAAGTCATATA | 9474 |
rs529961133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254904 | CCTGTTGGAGTTATG[C/T]AATTGAGCAGCCTTT | 9474 |
rs529982559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106255612 | CAGGATTCAATTATC[A/G]TATTCTAACCAATTA | 9474 |
rs529985549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213046 | GCATAGGTACAACAA[C/T]GACTACTACTACTAA | 9474 |
rs529989075 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106206087 | TATCATCTGAATGCG[A/T]CCCTCCAAAATTCAT | 9474 |
rs529997466 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271154 | GGCCTTAGATAATTT[C/G]GTTCTTTCTCATCTC | 9474 |
rs530049637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204190 | ATGTAACAAACCTGC[A/G]CATTCTGCACATGTA | 9474 |
rs530061286 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106296947 | TGACAGAGGAAGATG[C/T]TTCACAATTATTAGA | 9474 |
rs530071760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204984 | GTTCAGAGAAGAAAA[A/G]AAATGAATAGGGAAC | 9474 |
rs530081886 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243972 | CAGGCTTGAGTGTAG[C/T]GGCATGATCATGGCT | 9474 |
rs530087091 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302931 | CTAAATGCTTGTACA[A/G]CATTGTGAATGTAAT | 9474 |
rs530097566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106292777 | GGCTGGCCCAAAAAC[C/T]CGTAAATTTTAAAAA | 9474 |
rs530117463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253309 | GGCCCAGTGGGCTAG[C/T]CTCTGCGTCAGGGCT | 9474 |
rs530120491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211499 | GTGGATCATGAGGTC[A/G]GGAGTTCGAGGCCAG | 9474 |
rs530159182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106246349 | TATAGCACTTTATAA[A/G]AACCATTCTCTCTCT | 9474 |
rs530159533 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290375 | ACCCAGGATGAAGTG[C/T]GGTTGTCTGATCATG | 9474 |
rs530188926 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190830 | AATGGTAACTTCTTA[G/T]GTATATATTAAAAAA | 9474 |
rs530198272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275158 | AGCATTAAAGCATCA[A/G]TAGGAGTTAAAGGGA | 9474 |
rs530200807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106325205 | ATAAAGGTTTAAATA[A/G]CTGTGTTCCACAAAC | 9474 |
rs530229790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226533 | TAAATATGCGCAAAG[A/C]ACTAAAAAAAAGTTT | 9474 |
rs530233325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291392 | TAAGGCACCCACAGT[G/T]TTAACCACCATTGTT | 9474 |
rs530237451 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325767 | GGCAACGCTGCGGAG[C/T]CCTGGCAGCGCACCA | 9474 |
rs530264896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106232956 | CTGTTTCACCCCAAG[A/G]GTTCAGGGATAGCCC | 9474 |
rs530277826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284159 | TTATTTCCCTATTTT[C/G]CATATCAGAATTACA | 9474 |
rs530313453 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233407 | ACCTGAAGCAGAAGC[A/G]GCTTTCCAGGCCCTA | 9474 |
rs530382564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239266 | AAAACAAAATCTACA[A/G]AACACCTGGAAATAA | 9474 |
rs530400858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318507 | AGTTTTAAAGTCTTA[C/T]GTTCCAGCAAAGTTT | 9474 |
rs530403883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227110 | CCAAGAAGATAAACA[A/G]ACTAAAAAGAATAAA | 9474 |
rs530419178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246912 | TTAGAAATTCAAATG[C/T]CGGGCACTTTTCTAG | 9474 |
rs530436615 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106312123 | GGCGTGAGCCACTGT[A/G/T]CCTGGCCTGATCAGT | 9474 |
rs530439773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226508 | GACAAAGACTTTAAG[A/G]GAGTTATTTTAAATA | 9474 |
rs530453638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197174 | AAAGGAAGTTTAAAA[C/T]AACATATTTTAAAAA | 9474 |
rs530472656 | in-del | -/TTTTGACCTGCTCCAT | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106283496 | TAATCAGCACGGGAG[-/TTTTGACCTGCTCCAT]TTCTGACCTGGGCTG | 9474 |
rs530474698 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235866 | AATAAAAGGAATACA[C/T]TTTAAGTATACAGTT | 9474 |
rs530516475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324348 | GGATGTGCATAGGTT[A/T]TCTGCAAACACTACA | 9474 |
rs530534431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106319099 | TCTCTATTTCTGTTT[C/T]CTCATCTGTAACATG | 9474 |
rs530571412 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211383 | CACAGCAGGCAGAAT[C/G]TAACAATGACAAGGG | 9474 |
rs530614071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275107 | CTAAAACAATAAAAG[A/G]AGGAAAGCTTCTTAT | 9474 |
rs530644627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190115 | CAAATTTATCAACTA[C/T]CCCAATAATGTATTT | 9474 |
rs530692588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106254103 | GGTCCCTAGTAAATA[C/T]CAAACTTGCTCCCAT | 9474 |
rs530695230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106205975 | AAAAACGTAATATTC[C/T]TATTCTTAAAAATTT | 9474 |
rs530707303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305149 | ATGCTTGGGATTATT[C/T]TTCCCTTCTCACACA | 9474 |
rs530738017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106212331 | CATGCCCAAAAGCTA[C/T]CTTCCAAAATTAAAA | 9474 |
rs530747078 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106297957 | AGAGGGAGACCCTGT[A/C]AAAATCTATTTTTTT | 9474 |
rs530798933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310805 | ACCATATAATATTTG[C/T]CCTTTAGTGCCTGGT | 9474 |
rs530809211 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264682 | AGACAGTGGGAGCCA[A/G]TATATTCAACATTCT | 9474 |
rs530809533 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106276446 | TCCAGCCTGGGCGAC[A/G]GAGCGAGACTCTGTC | 9474 |
rs530818517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262180 | CAGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 9474 |
rs530855787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268426 | CACTTTTACACTGTT[G/T]GTGCGAGTGTAAATT | 9474 |
rs530867618 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106254409 | CCTAGAAAGTTCTAC[A/G]TACTTCAGCCCTAGA | 9474 |
rs530875737 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106304457 | TAATGAATAAACAAT[C/T]TGTGGTATAACCATA | 9474 |
rs530901814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210656 | GATGACGATGGATTC[A/G]GCTTATGGTTCCAAT | 9474 |
rs530955597 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106310130 | TTTGTCTGTTTTGTT[A/C]AATGCTACATTTCCA | 9474 |
rs530955909 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106295666 | CCTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 9474 |
rs530958895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106189414 | ATTTGAGACCAGCCT[A/G]GGCAACAGACCCCAT | 9474 |
rs530974692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252616 | CCACTTAAGCTTTAC[A/G]AGAGGTAAAAACTCA | 9474 |
rs530983494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106260426 | ACACTAAATGTAAAA[A/G]AGCTCCAGGAACTTA | 9474 |
rs530995269 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319489 | AGTATAATCTCCAAA[A/T]CTACTAAACATACTA | 9474 |
rs531001945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232061 | CTGCCCCAGGGGACG[C/T]AGGTCCTCTGAGTCA | 9474 |
rs531008138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230310 | CGAATTTGCCTAAGA[A/G]CTGTTGTTTATGGGA | 9474 |
rs531069346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106296224 | TCACTTTAAAAAAAA[A/G]AAGATAAAACTTACT | 9474 |
rs531095336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282631 | AGCATGACTTTAACT[A/G]TAGGCTTTTCATATC | 9474 |
rs531100544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106196670 | AGGGGTTGCAGTGAG[C/G]TGAGATGGCATCACT | 9474 |
rs531130491 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241528 | AAACAGGGTGTACAC[A/C]CATTTCAACATTTAC | 9474 |
rs531132595 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106239240 | AACTAGAAATGGAAA[A/C]AAAATAAAGAAAAAC | 9474 |
rs531133999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195703 | TGACAGTTTGCATGG[A/G]GAGAAGTCTGTCACA | 9474 |
rs531135957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204095 | AGTAGGGGGCTAGGG[C/G]AGGGATAGCATTAGG | 9474 |
rs531143743 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226665 | AAAAACAGAATCATA[C/G]AGTATATTCTCTTTA | 9474 |
rs531176807 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106208046 | GCAGTGAGCCGAAAT[C/G]GCGCCACTGCACTCT | 9474 |
rs531183646 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190742 | AAGAATTACATATAG[-/A]AAAAAAATAAGAAGA | 9474 |
rs531192319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299164 | TCCTGGACCTAGCTG[A/G]ATACCAAAATTCGCA | 9474 |
rs531194680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307614 | TTGTGATAGCTCACC[A/G]CAACCTCCACCTCCC | 9474 |
rs531203755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246222 | AAAAACTGCCCAAGT[G/T]CCTTGACACATTAAA | 9474 |
rs531246961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257285 | AAGTAGAAGGTGAAC[A/G]CTCTAAAATAATGAA | 9474 |
rs531351989 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310999 | TTTTTATCTATACAG[C/T]TTAAAAGAATACATA | 9474 |
rs531354515 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306805 | GTTGCTCTGTTTACA[A/C/T]TTCCTTTAAGTCGCC | 9474 |
rs531355279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314512 | CAGTGAGCCGAGATG[A/G]CACTACTGCCCCCTC | 9474 |
rs531371049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287337 | TCAAGGAACAGTCAG[A/G]ACCAATGCAGGGCTT | 9474 |
rs531372168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106249387 | TTTTTCGCTTGGCAT[A/G]ATATTTTTGGTGTCC | 9474 |
rs531405741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235614 | CAATCAGGTAGTAAA[C/G]AGAGCTCACTAAAAT | 9474 |
rs531406229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106321865 | ACCTTCTTATCACCA[A/G]TATTAGTACAGTTAG | 9474 |
rs531412075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106243610 | CTGAGGCAGGTGGTT[C/T]ACCTGAGGTCAGGAG | 9474 |
rs531413475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256570 | GCAATTTCATCATGC[A/G]AACATCATAGAATGT | 9474 |
rs531450945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106263464 | CTGAAGAGAGGAGCT[A/G]ATCCTGACAAGACGG | 9474 |
rs531487463 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186104 | GATAACAGAATTTCT[C/T]TTTTACTTTCTTAAT | 9474 |
rs531493764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193533 | GTAATTATAAAAAGC[A/G]AAGTGTATTAAATTA | 9474 |
rs531498664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106278777 | ACAAGGAGGCAACAC[A/G]ACTATGTGCTTTGCT | 9474 |
rs531533234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229560 | AAAGATAGAAATAGT[A/G]AAAAAAAACAGTGTG | 9474 |
rs531535679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286637 | GGCAAAGGTGATGGG[A/C]TGTTACCCCAGTGAT | 9474 |
rs531570529 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248264 | AATGATATAAATTAT[C/T]TGTTATTAAAAATGA | 9474 |
rs531572132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235319 | CGTGGACCCCTGGAC[C/T]GGCCTACTAGCCCAT | 9474 |
rs531572856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243746 | TGAGGCAGGAAAATC[A/G]CCTGAACCCAAGAGG | 9474 |
rs531594610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293371 | ATTCTTTATCAGCCA[C/T]GTGAACTGTTATGTC | 9474 |
rs531599425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242772 | ACTAAATTAAAAGCA[A/G]TAATATTCAGTTTAC | 9474 |
rs531612821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284413 | CCAGGCTGGGTTGCA[A/G]ACATGCCATCAGGAA | 9474 |
rs531634162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233677 | AGAGATCTGTGTAGA[C/T]ATCTCATAACGTGAA | 9474 |
rs531637957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249814 | ATTCTGGCAGGCATC[A/T]AGAAGTATCTCATTG | 9474 |
rs531651572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271957 | AGGAAGTTTTTAATC[C/T]CAGATAAATATGCAT | 9474 |
rs531664636 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208310 | CTACATTATAGTTTC[C/T]GAGATAATAAAATGC | 9474 |
rs531687564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240237 | TATTTATATTTTTTA[C/T]ATAGATATCATAAAA | 9474 |
rs531690313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191818 | ACAAAAAGTAAAGAG[C/T]GATTGTAATTCTCTT | 9474 |
rs531691252 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196423 | CTAAACCTATTTCTG[A/C]AATTAAGTGGTTAAG | 9474 |
rs531697026 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226689 | CTCTTTATATCAGCT[C/G]TTTTTACTCAACACA | 9474 |
rs531697409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284878 | ATCAAGTTATTTCCA[A/T]ATTCCGTATATTAAA | 9474 |
rs531702742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106247969 | AATGAGTACCAAATG[C/T]ATATGAGTCAAATAT | 9474 |
rs531720791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233973 | CCCACACCCATATGC[A/C]CCACAACTGCTATAA | 9474 |
rs531737610 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257696 | CACTCTAGGCCTGGG[A/G]TATCACAGGAATTTA | 9474 |
rs531745128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269925 | GGAGACGCCGAGAGC[A/G]AGCAAGGGCTGTGAG | 9474 |
rs531763334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262899 | CAGGGCCCTGGGTTT[C/G]AAGCACAAAACTGGG | 9474 |
rs531772284 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296987 | ACAAAATACAAAGAG[A/G]GACAGCAGTACTCTA | 9474 |
rs531785201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313219 | TGTGTGGGATGCAGA[C/T]AGGTTTTGCAGATTT | 9474 |
rs531797106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298319 | CCAGATGGTAAATGA[C/T]GACAACTCCTTTGTC | 9474 |
rs531815007 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106309742 | AAATACAGATGTGAC[-/A]TTAAAGTCTCTTTAA | 9474 |
rs531828031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198994 | ATTATAATAAGCACA[C/T]GAAAACATGTTCAAT | 9474 |
rs531830956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191148 | ATATACATATATATG[A/T]GCTGAGCTCCTCTCC | 9474 |
rs531863893 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251414 | ATATATAGTTTTCTT[A/G]TATTTTATAGACACT | 9474 |
rs531868389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198495 | AGAAAATGAAGACAA[A/G]GCTGGGCATGGTAGC | 9474 |
rs531874803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277808 | GACAGAGTGAAACTT[A/C]GTCTCAACAAAACAA | 9474 |
rs531876803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106269329 | AAGGTTCTCCACGTC[C/T]CCACCAGACTCAGGA | 9474 |
rs531912241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276937 | ATAAAAATGTGGTAC[A/G]GGGCCTAGTGCTTAA | 9474 |
rs531917129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222017 | GTGCCTCAGCCTCCT[C/G]AGTAGCTGGGATTAC | 9474 |
rs531956779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228702 | CCAAAGCGGTAATAT[G/T]GGACCACTTTTGCTT | 9474 |
rs531965434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206831 | TTTCAACAGCTCTCA[C/T]TAGCCCGATGTTAGA | 9474 |
rs531972748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106308265 | CTAGACTAATGACTT[C/T]TATCCTCGCAGGACT | 9474 |
rs531993742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228298 | CAGGCCTGCCACTGA[C/T]TTCCATCCCTCTGGA | 9474 |
rs532010351 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234809 | CTACTCAGTTCTACT[A/G]CAAACTATCTCAAGA | 9474 |
rs532022112 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278871 | GACATAATTTATCAC[C/T]GATCATAAGCTCATC | 9474 |
rs532038055 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326540 | CAAGATAGGGCCACC[G/T]CAGTCCCGCCTGGGC | 9474 |
rs532076086 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326957 | GTAAAGGGTAAATAT[G/T]GTGTCCCAAAATTTT | 9474 |
rs532087805 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218621 | ATGTGTAGATCCTTT[C/G]AAAGCCACTCTACCC | 9474 |
rs532107005 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106309543 | GAATATAAGTTATTC[-/T]TTTATAAAGAAATAA | 9474 |
rs532166760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106234644 | TGCTTCCTCTCATTC[C/T]TAGTGCCCCCATGAC | 9474 |
rs532184987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200143 | CTTGACTAAGGAAAA[C/T]TGCAATATTCTCAGG | 9474 |
rs532189894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263241 | GAGGTCTGGACTGAG[C/T]GGAATTCACCACAGT | 9474 |
rs532189900 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106255668 | TTAAGCCAGGTAATA[A/T]AAAAGATTCAAAACT | 9474 |
rs532203651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242458 | GTTTAATGGGTATAG[A/G]GTTTGTTTTGCAAGA | 9474 |
rs532226123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262841 | TTTCCCATGGTTTCT[A/G]CAATCTGCAGATCAG | 9474 |
rs532229728 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188164 | AGTACCAGTACTTTG[A/G]GAAGATTTTTTAAAC | 9474 |
rs532236539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293238 | CACAGGAAGACTACA[A/T]TCTACAGTTACGTGC | 9474 |
rs532258141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269278 | GCTAGATACAGAGTG[A/C]TGATTGGTGTATTTA | 9474 |
rs532263345 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283267 | ATTTTCTTTTAATGT[C/T]TTTATCAGGTTTCAG | 9474 |
rs532306656 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324364 | TCTGCAAACACTACA[C/T]CATTTTATATCAGGG | 9474 |
rs532312923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106249035 | AGAAACATGGAACTG[A/G]CACTTATGAAGTGCC | 9474 |
rs532320095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106207537 | GAGACCTCATCTCTT[A/T]AAAAAAAAAGAAAGA | 9474 |
rs532333359 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305444 | TTTAGTTTTTTTTTC[A/T]TGTCATTGAGAACTG | 9474 |
rs532343278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291451 | AACGGGAAGGGCCAA[C/T]AACATCCTGATATTA | 9474 |
rs532369487 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106242000 | CCTGTTCATGGCAGC[A/G]TTATTCACAATAGCC | 9474 |
rs532375902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190374 | AACCCATTCATGAGG[G/T]CAGAGCCCTCATGAC | 9474 |
rs532454863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297189 | CTTCATTACATGATA[C/T]TTTATGACAAAAACC | 9474 |
rs532455539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256490 | CGTTAACAACCTCCA[G/T]ATGTAACAAAAAACA | 9474 |
rs532479636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253963 | GCAGATTCCTACCAG[A/G]CCCATTCCACCCCCT | 9474 |
rs532512885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198316 | GAACAGGTAGTTAGG[A/G]AAGAGACTTTTTACT | 9474 |
rs532532015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106240111 | AATGCTCCCACCACA[A/G]AATCCCAAACAGCTG | 9474 |
rs532554269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268555 | GATTATAAATCATTC[C/T]ACTATAAAGACACAT | 9474 |
rs532562097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205834 | AATGGTAAAAACAAG[A/C]AAATGCTCAGCAAAG | 9474 |
rs532576869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220434 | CACAAGAACTGAGGC[A/G]TATACTTCATTAATG | 9474 |
rs532678907 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195894 | GTAGAGCAGCCTAGA[A/T]ATTTAACAGAACAAA | 9474 |
rs532700114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284250 | TCATTTGATGACATA[C/T]CAAACTGCTTTCCAA | 9474 |
rs532702426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106205116 | AAAGGCTTTTTCTGA[C/T]GACTAATGGAAAGCA | 9474 |
rs532738004 | in-del | -/GGTTATTAAACTGA | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317571 | GGCAACAAGAATTCT[-/GGTTATTAAACTGA]GTCCAGTGCTCTTTC | 9474 |
rs532762273 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277818 | AACTTCGTCTCAACA[A/G]AACAAAACAAAACAC | 9474 |
rs532771088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227447 | CAAAGAATAAAAAGA[C/T]TGGCTGAATGTGGTG | 9474 |
rs532771901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287505 | CTTAACAAATGTGAG[C/T]TCTTACCCTTAATCA | 9474 |
rs532773229 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199478 | AGACTATATGCTGTA[C/T]GGTTCAATTTATGTG | 9474 |
rs532783994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294551 | GGCTGGGTACTGTAA[C/T]TCAAGCCTGTAATCC | 9474 |
rs532787856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236557 | AACGTGAAGTAGTAT[C/T]TCACTGTTATTTTCA | 9474 |
rs532800152 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280005 | TTGGCCCATTTTGTA[C/T]TTTTCCCAAATAATT | 9474 |
rs532850489 | in-del | -/AGAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251730 | GAAAGAAAGAGAAAG[-/AGAA]AGAAAGAAAGAAAAG | 9474 |
rs532875280 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106250992 | ATGTCCAGATACGCA[A/C]GTCTCTCAGCAAGGT | 9474 |
rs532876343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191074 | ATGAAGATGCCTATA[C/T]AGATGTATGGTTTGA | 9474 |
rs532890679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106186940 | ATTACTGTGCTTACT[G/T]AAGATTGACGTTAAT | 9474 |
rs532940016 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308062 | AATGTCAAGAGATGA[C/T]TTTTCATAAGGGAGT | 9474 |
rs532946733 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229216 | GGAAGCTCTATGCTG[C/T]GCCCTTAGGCATCTA | 9474 |
rs532956567 | in-del | -/ACA | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106294161 | GCTCACCCTGTACTC[-/ACA]ACAAGGGCAAAAAGA | 9474 |
rs532956662 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323366 | CTTGAGCTCAAGGGG[C/G]TCAAGTGATCCTCCC | 9474 |
rs532968217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106202915 | CAATCTGCCGGCTTC[A/G]GCCTCCCAGAGTGTT | 9474 |
rs532989332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316821 | TCTCTACAATTTAAT[C/G]CCACCAATACTTCCA | 9474 |
rs533001122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294015 | GCATCATATTCTTAC[C/T]ATTTGAGCATCACAA | 9474 |
rs533014607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301283 | CTTGTAAGCTCTCTA[C/T]AAATCGACAACAACA | 9474 |
rs533016589 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106303344 | CTCCCCAAAACCCAT[-/A]AACTACCAACACTCA | 9474 |
rs533018555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243793 | CCGAGATTGCACTAG[C/T]GCACTCCAGCCTGGG | 9474 |
rs533035268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194323 | ATTGCTCAAATATTA[C/T]CTCAAATCACGAGAT | 9474 |
rs533053720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106272582 | CTTCCTCTACAACTC[C/T]AGTTATAAATGTAAC | 9474 |
rs533087711 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202027 | ATCTCCTAGTGTGTG[C/T]AACTGTCCATCTGCA | 9474 |
rs533089602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280550 | TTCTATAACTTCACT[A/G]ATTCTTTTAGGCAGC | 9474 |
rs533109667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106265637 | AAGTGCAAAATAATG[A/G]AAATCATAATAAACA | 9474 |
rs533112873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187673 | AAGGAGAAATACCCT[A/G]CGTTTTCCTTTCTGC | 9474 |
rs533119895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316371 | CATAAAGATTATCCA[C/T]TTCAAAAAAAAAAAA | 9474 |
rs533130327 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106216984 | AAAAAGTTATCATAT[C/G]GGTGGCAGGGGAAAT | 9474 |
rs533155345 | in-del | -/AAG | 0.021333 | 0.101051 | intron-variant | ATG5 | GRCh38.p7 | 6:106251765 | AAGAAAGAAAAAGAA[-/AAG]AAGAAAAGAAAAGGA | 9474 |
rs533175775 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184992 | ATATTGCTATTTTTT[G/T]CCTGCCTTTACTAAA | 9474 |
rs533179233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224382 | AAGGGAATAAATGAA[A/G]ACAGTTCTGGTCCAT | 9474 |
rs533207513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228911 | CACTTTCAATTTTCC[C/T]GGGGAAGCCAAGGGC | 9474 |
rs533209355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106235285 | GGAACCCCAGATGAA[A/G]TCCATGACTAAGATC | 9474 |
rs533263965 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185999 | AAGATTGCATACCAA[C/T]AGACAGACTGTAAAC | 9474 |
rs533265951 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327193 | CAGACAAAAGTATAT[A/G]AAATTTCCTTTAAAA | 9474 |
rs533294106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106323080 | CTTGCCACCAGGCTC[A/G]GGTTTGTTTTTTTTG | 9474 |
rs533302129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193368 | TATCTTTATTATATT[G/T]TCAGAGCTTTGACTC | 9474 |
rs533358494 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194784 | TCAGGTGATCCACCC[A/G]CCTAGCTTACCACGT | 9474 |
rs533365695 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106215808 | TTCAAATGACATCAT[C/T]AAGAAAATAAATCCC | 9474 |
rs533373165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314663 | TCTCACATACTCTTA[C/T]ATACTATTACAAAGC | 9474 |
rs533397147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106257913 | GTGTAGAGTGAAATC[C/T]ATCAAACCCCTTGCT | 9474 |
rs533432816 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106257390 | ACTGGCAGCACATTT[G/T]TTTATGACAGTATCA | 9474 |
rs533440547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106264851 | GAAGGAAGCACTACA[C/T]ATAGAAAGGAAAAAC | 9474 |
rs533447917 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205524 | GTACCCCATAAATAA[C/T]TGCAACTATTATGTA | 9474 |
rs533462417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106278730 | TTCAATTATCCATTT[C/T]TATAAAATGTTACAT | 9474 |
rs533491557 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224912 | CAAAACAAAACAAAA[C/T]ACAGAAATACATCAA | 9474 |
rs533499667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106278241 | AGCCACCACACCCAG[C/T]CAAAAATGTTTTATT | 9474 |
rs533501440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315388 | GGGCTATTCAGTGAA[A/C]AGGCAGGATGTCATC | 9474 |
rs533503028 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185087 | CTGTACTGGCTATTC[A/T]TTTTGATTAAGCTTT | 9474 |
rs533516603 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185610 | GAAAAACACTAGCTT[C/G]GAAGGAATGGGTTTT | 9474 |
rs533518669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286820 | CAACAAGAAGATAGG[A/C]CCCTCAATCCTACAA | 9474 |
rs533530414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208740 | ATGAAAACATAAGCC[A/G]CAGGCTGGGAGAAAA | 9474 |
rs533543524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272448 | CTCGATCTTGATCAC[C/G]ACATTCTAGTCAGTT | 9474 |
rs533552386 | in-del | -/CGC | 0.00279162 | 0.0372561 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327573 | GGGCATGGTGGCATG[-/CGC]CTACAGTCCCAGCTA | 9474 |
rs533561043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106192997 | CGAGGTCAGGTCAAA[A/G]AGGGTTAAACCAAGC | 9474 |
rs533587513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300447 | CACAAAGAGTATTAA[A/C]TTCTGAGTCATTCTA | 9474 |
rs533589617 | in-del | -/ACT | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106322706 | TTGAAATGCCCCAGG[-/ACT]ACTCAGTCCTTGAAC | 9474 |
rs533613012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106313384 | GGGCAGACACCTGAC[C/T]AAGGATACATAAACG | 9474 |
rs533695893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200246 | CAAACCCACTGTTCC[C/T]AATTCTACTACTTAG | 9474 |
rs533733426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215262 | AAGTGAAATTCTGTT[A/C]TCTTGATGCCCAGTT | 9474 |
rs533743486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315586 | AGCTCACATATAACA[C/T]ACAATAGCTCAGTGA | 9474 |
rs533777343 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235691 | CGCCTGAGAGCACAG[A/C]GGGAAGGACAATGAT | 9474 |
rs533815893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234888 | AGATCAACTTAACTT[C/T]CTAGCATCAGTAGTC | 9474 |
rs533826649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321548 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCGTGT | 9474 |
rs533844313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271362 | ATTAGGTCATAAGGG[C/T]GGAGTCCTCATAAAT | 9474 |
rs533853719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242073 | TGTGGTATGTATATA[C/T]AATGGAATATTATTA | 9474 |
rs533862885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322006 | TCGCACTTTAAATTC[A/G]GCATATTTTGTTATT | 9474 |
rs533867426 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186160 | CCACTTTCATGAGCT[A/C]AAGTTCAACCATGGT | 9474 |
rs533891487 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106262466 | AGAAGCTAACAGACA[A/T]AACAAAAAAGGATTA | 9474 |
rs533935284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221454 | ACTTTGGGAGGCCAA[C/G]ATGGGCGGATCACTT | 9474 |
rs533936304 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106192264 | GGTAAAAAAAAAAAA[A/C]CTTTCAAAATCTTTA | 9474 |
rs533936589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106264426 | CACACTTCGGGGTAT[C/T]ATCCAGGAGAACTTC | 9474 |
rs533972299 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106228362 | TGAGACGCCCATTGC[C/T]GATCCCGACTGGGCT | 9474 |
rs533994656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308041 | GTGTCAGAAATAAAA[C/T]TGAATAATGTCAAGA | 9474 |
rs534025347 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106268918 | GAACATTAGGACAAA[C/T]ACCTAATGTATGCAA | 9474 |
rs534032313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106277158 | TAATTTTGTAAAAGG[A/G]AAGTTTAACAAATAC | 9474 |
rs534036651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233708 | CGGCATACTCACTGC[C/T]AAAGGAGACTTGTGG | 9474 |
rs534064986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222359 | AAGTTATTTTATTCC[C/T]AAGTTTGAGACTTCA | 9474 |
rs534087817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235343 | AGCCCATGCTCCAAT[C/T]GTAATGATATCGAAC | 9474 |
rs534101655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229081 | ACCACGACTTTCTTG[A/G]AAGTGTAGCCCCAAA | 9474 |
rs534144558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106299217 | ATGGCATAGTATTTG[C/T]ATATAACCTACACAC | 9474 |
rs534177214 | in-del | -/TTTAT | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106322919 | TCCTCTCTCCTATCA[-/TTTAT]TTTATTTTATTTTAT | 9474 |
rs534178611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212678 | ACTCAAAAAACCCTA[C/T]TGGCAATTACTAGGG | 9474 |
rs534188808 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106313302 | TTCTTCATGAAAGAG[A/G]AAGTGAGGTCACCTG | 9474 |
rs534192604 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206063 | TCAATTTGGGGAGTT[A/G]GTTACTTCTATCATC | 9474 |
rs534229963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220617 | CAAATAGTTATTTTA[A/G]AAGTATGAGTAATTA | 9474 |
rs534282150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266485 | AAGAGGGACTCCTCC[C/G]TAACTCATTTTATGA | 9474 |
rs534318752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319608 | CATGCTTTAGGACCC[A/C]GCTCAAAATAACCTT | 9474 |
rs534336470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276357 | TAGTCCCAGCTATTC[A/G]GGAGGCTGAGGCAGG | 9474 |
rs534338020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217120 | CATAAAAACAAATTT[A/T]AAAAAAATTAAAGTC | 9474 |
rs534382555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298713 | TCCATAATTAACATG[A/C]GGTTCAATACAAATT | 9474 |
rs534388758 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186307 | TCAGTGGTCCGGTAA[G/T]TCTTTCATGTCACAG | 9474 |
rs534406756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265910 | GAAAGATCTAAAATC[A/G]ACACCCTAACATCAC | 9474 |
rs534432948 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199989 | TTTAATAATTTGGGT[-/A]GTCAGTGGTCTCTTC | 9474 |
rs534440117 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254652 | GCAAGACACTTACTG[A/T]GCCTGACACAAATTA | 9474 |
rs534452728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272683 | TGCCTGTCATATTTA[C/T]CCCAGCGTCCCCTGT | 9474 |
rs534499642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295870 | TGTCCAGCCCAAATA[A/G]CTCTTTAAGGAAATA | 9474 |
rs534503944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196057 | GAATGCTTTTCATTT[A/G]CGTGTCTGATGTTCA | 9474 |
rs534550964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253389 | ACACATCTTGGCAGA[A/C]GGTTTCTACCCAGGG | 9474 |
rs534551299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306410 | TTTCCAGAGTTCCTC[A/G]ACTGGGGGCGGTTCT | 9474 |
rs534566110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317263 | GATTCAATATACTTA[A/T]CCAAATAATATTTCT | 9474 |
rs534570863 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106309641 | ACAGGAAGTATTATC[G/T]CCCCTGTTTTAAATA | 9474 |
rs534577044 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227642 | CTGCACTTCAAGAAA[C/T]GATCAGTACCTTGAA | 9474 |
rs534606415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310312 | GCAATTTTCTGTTCC[A/G]TTTGGCCTGTGGGAG | 9474 |
rs534608041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217973 | ATAAACATTTTAATA[C/T]ATAGCAGGCTTAACT | 9474 |
rs534644001 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222279 | ATCTATCTTTCAAAA[A/T]GAGGTATTAACTATT | 9474 |
rs534645660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106225077 | TAATAATTCCAGCTA[C/T]AGTGTGCAATTTAAT | 9474 |
rs534694631 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276782 | GATCCTCATCTTTTT[A/C]TATTTAGGCTATCTT | 9474 |
rs534707560 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232669 | AGTAAAAGCATGCAA[C/T]AGCCCCTACAATAAT | 9474 |
rs534739313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229639 | TTGAAGGTCTTCTCC[A/G]CGACCCTATAACACT | 9474 |
rs534753044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216100 | CTATAGAAAATAAGC[A/G]TTGGCAAGGATGTGG | 9474 |
rs534754905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208339 | GCACAACACAATTCT[C/G]ACACATAACAATTTG | 9474 |
rs534766969 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285757 | TGCAACTTTATTTAT[A/G]GTCATCACTAAATCT | 9474 |
rs534796839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303693 | TCCAACAATGTATAA[A/C]ACTTATTACATTCCG | 9474 |
rs534800988 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312309 | GAGTAGTTCTTCTTG[C/T]CAAAACAGGAAGGGA | 9474 |
rs534804455 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259309 | AGGGATACGTGATAT[A/C]CATAGTGTATCCTGT | 9474 |
rs534848895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308668 | GGTTAAGATGTTTTA[A/C]TATTTCTTATGGGGC | 9474 |
rs534868554 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263709 | CTGGTGATACCCAGG[C/T]GAACAGGGTCTAGAG | 9474 |
rs534876984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280863 | GACTCAAGTCCTACA[C/T]TTTAACCACTGTACA | 9474 |
rs534882082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230919 | CTTTCTTTTCATTAA[C/G]AGACAACTCGCAATT | 9474 |
rs534918178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230328 | GTTGTTTATGGGAAT[A/G]CATCTTGATGGAGCA | 9474 |
rs534920173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236823 | ATTATTATATGCCCC[A/C]TGAAAGCAAACACAG | 9474 |
rs535039659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201505 | TTTTGAACGAACTTG[C/T]AGATTGTCAAAGCCT | 9474 |
rs535047688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265370 | AGTTCTTCAAGATCT[A/G]CGAAGAGACTTGAAC | 9474 |
rs535047834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106272603 | TAAATGTAACAATTA[C/T]GTAAAAGTGATCTGT | 9474 |
rs535052460 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234781 | GGTTCTGGCATTGGC[A/G]GTACCACAACCTCTA | 9474 |
rs535054708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194389 | GTATCTGCTTTATAC[A/G]GTCAGCATGAGATTT | 9474 |
rs535078894 | snp | C/G/T | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106200975 | CACCCAGGCTCAAGT[C/G/T]GCTTATATAGAATGG | 9474 |
rs535119421 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199745 | GAGTCTAAGATAGTA[C/T]TATAATCAACTTAAT | 9474 |
rs535162720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299998 | TACTGACTTACTCTA[C/T]ATGTAGGACAAACAC | 9474 |
rs535175275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106230283 | AAAAGCTTACTTATA[C/T]CCTCTCTGAAACGAA | 9474 |
rs535192818 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106224996 | ATACAGGAGGCATGA[C/T]AAGCCATCATCATTG | 9474 |
rs535204238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188106 | TAATGATTTGTTTTC[A/G]TAATGAAATATTAAG | 9474 |
rs535229163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280116 | ATATTGGCAAAGATG[G/T]GGAATGGAGCCCTCA | 9474 |
rs535234799 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106279953 | CACTGAAATAACCCA[A/G]AATACTTTAAAATTT | 9474 |
rs535242712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187102 | GTAAAATAGAAATGT[A/G]ACTAGAAATCAAGAA | 9474 |
rs535252053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252123 | TGGATTACAGGCATG[A/G]GCCACCGTGCAGAGC | 9474 |
rs535276213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203190 | TCTGACAAAAACTGT[G/T]AGCAGCACTACATCG | 9474 |
rs535341734 | snp | A/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202725 | GGAGTGCAGTGGCGC[A/G/T]ATCTCAGCTCACTGC | 9474 |
rs535393539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315633 | TATGTGTGCATGTTT[A/G]TATGTTCTTTAAGCT | 9474 |
rs535412561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249617 | ATGTACCTAGGAGTA[G/T]AACTACTGGGTCATT | 9474 |
rs535423701 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ATG5 | GRCh38.p7 | 6:106309616 | TATAAGAAAAAGCAG[C/T]TTTTCCCCCACAGGA | 9474 |
rs535437204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257517 | GACCACTATCATACA[C/T]GCAGTCCACTGTTGA | 9474 |
rs535458769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307897 | AAAAGGAAATCAATA[C/T]ATTTTAAATACTCTA | 9474 |
rs535465245 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | ATG5 | GRCh38.p7 | 6:106208272 | TGTAAACACATATGT[A/G]TATGTATAAATGGAG | 9474 |
rs535468270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230791 | GCAACGATATACTCT[C/T]TAAGGGGGAGAAACC | 9474 |
rs535469275 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256440 | TGGCATCTGTACTTT[A/T]GAAAGCTCCCCAGAT | 9474 |
rs535478708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223974 | ATTCCACAGTTACAT[C/T]TGTCAAAACAAAAGG | 9474 |
rs535516947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106222998 | TGAATAAAACAATGA[C/T]CTAGCTTAGTAAATA | 9474 |
rs535547402 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106229792 | CATTCAATCTGTAGC[A/C/G]GCAACTGCTTTGCTA | 9474 |
rs535564957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264254 | ATATCAGAGATTGAA[G/T]ATCAACTTACTGAAA | 9474 |
rs535581060 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282034 | CAAGTTGAGTATAAT[A/G]TGAATTTTATGGTTG | 9474 |
rs535592680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259924 | CCATGGAATACTATG[C/T]AGCCATAAAAAGGAT | 9474 |
rs535624294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210148 | GTTGGACAGTGACTC[G/T]CAACACAAATGAGTG | 9474 |
rs535624618 | in-del | -/CTAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269561 | CCCGCGGGAAGGCAG[-/CTAA]CTAAGGCCAGGTGAG | 9474 |
rs535652078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302669 | ACATCAACAAATTTA[A/T]AAGATCCAAAATTAC | 9474 |
rs535690054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243838 | TTCATCTCAAAATAA[A/G]TAAATAAGTAAGTAA | 9474 |
rs535723721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251121 | CTTATCAACATCTCA[A/G]TTTGCTTGCTCTGGA | 9474 |
rs535725624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106243289 | ATTCTGAGGATTATG[A/G]AAGTAAACAAAACGA | 9474 |
rs535760292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250311 | GTGACAGGCTTTAGG[C/T]CTTCCTTACTCTAAT | 9474 |
rs535771036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258419 | TAAAAACAAACAATA[C/T]TAGAGTGAGAAATAG | 9474 |
rs535867919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206378 | CAGAACTGTGAGAAA[C/T]AATTTTCTGTTGTTT | 9474 |
rs535868742 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258375 | AAGGAGGCCCTGAAT[-/A]AAAAAAAAAGGCTAG | 9474 |
rs535905595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219601 | TAAAGTATACAAGAG[A/G]GTATGCATAGGTTAT | 9474 |
rs535907424 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106211316 | TAAAACTTAAAATGG[C/T]CTTAATTAAAAGCCA | 9474 |
rs535919699 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106255630 | TTCTAACCAATTAAG[-/AAT]AATTTATTTCAAATG | 9474 |
rs535983855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307034 | TCAAAGGATTAGAGA[C/T]GGGACCCAAAATACA | 9474 |
rs536002219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303908 | TAAAATTAAGAACAC[C/T]AGAAGATGTCCACTC | 9474 |
rs536012615 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206922 | GCTGTAAACGTTGAT[C/T]TAGTATATATAAAAT | 9474 |
rs536016795 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258159 | CCCCATCTCCTCAAA[C/T]GGCAGAGATGACCAA | 9474 |
rs536052029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202382 | AAACAACACAAAAAG[A/G]TATCAACAAAAGCAT | 9474 |
rs536060109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193954 | GCAAGTGTGTGTTTC[C/T]CATTTTGGGAACAGT | 9474 |
rs536067335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106198588 | TTGAGACCAGTCTGG[C/T]CAACACAGTGAAACC | 9474 |
rs536067480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283971 | CTTTCACTTAACATG[G/T]TATTTTCAAGGTTGT | 9474 |
rs536085718 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265815 | AGAAAAAAGAGACAA[C/T]GTACCAGAATCTCTG | 9474 |
rs536093192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235478 | TTTTCCTGTTGAGTG[A/G]GGGGACTGAGAGACA | 9474 |
rs536094483 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209294 | CCCATTAAAACAGGT[A/G]AATGCTTATAAACTG | 9474 |
rs536102252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233141 | CCTGTGGCTACAAGG[C/T]TTCCAAACCAAAGGC | 9474 |
rs536168488 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231828 | GAGCAGGCAGAATGG[A/G]ACAAATGGGATAAAA | 9474 |
rs536181027 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231746 | AAAGTCTGCCTTAGG[C/G]CCGGAACAAAACTTA | 9474 |
rs536254788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106195878 | AGAAAAGGATGTACA[C/T]GTAGAGCAGCCTAGA | 9474 |
rs536289282 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188728 | AAGTAGCACTGATTC[C/T]CTGGTTTAGAAGCTG | 9474 |
rs536297460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295685 | CCTCCCACCTCAGCC[C/T]CCTGAGTGGCTGGGA | 9474 |
rs536344200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261720 | TAATTAGGGTGATAA[C/T]GGTAGAGATGAAAAG | 9474 |
rs536360885 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213247 | GCAAACAACTGTAAT[A/G]CAGTGTTATGTGATA | 9474 |
rs536390982 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106313718 | AGAGGAATATATGTA[-/C]TATTAATATTAAAAA | 9474 |
rs536395083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195206 | TTCATATGATGAAAT[A/C]AGACAAAATTCTTTC | 9474 |
rs536435305 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263201 | TTACTAGGCAGTTTT[C/G]CTCTGACAGTGCTAA | 9474 |
rs536448342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318596 | TTATTTCCCATATAC[C/T]ATTGTTGCTTACATG | 9474 |
rs536448561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311572 | GCACATTTGAGTGAA[A/G]TCTAAGATGCTGAAT | 9474 |
rs536459972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190628 | ATGTCCACAAAGCAC[G/T]TTTAGAAACCAGCAT | 9474 |
rs536473985 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237546 | GCCTTGTCTACCCCA[A/C]AGAAGTGTTATGAAA | 9474 |
rs536489662 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228126 | TTGGTTATTAGAAAA[C/T]AGCTTTATTGGGCTA | 9474 |
rs536515859 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG5 | GRCh38.p7 | 6:106225440 | GCAATATACTGAGTT[A/G]AAATTTTTATATTTT | 9474 |
rs536524805 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318524 | TTCCAGCAAAGTTTA[C/T]CAAAGTTCTACAGTA | 9474 |
rs536529381 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191294 | CCAATATACAACACA[-/G]GTAAAGATATGGCAG | 9474 |
rs536551478 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291827 | AATTCATGCATACCA[A/G]CACTATGTGCTCTAT | 9474 |
rs536579053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324411 | ACTTTGGTATCCAAG[A/G]GAGGTCCTGGAACCA | 9474 |
rs536587032 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106321396 | CGGAGTCTCGCTCTG[C/T]CGCTCAGGATGGAGT | 9474 |
rs536592615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197763 | ATGCCCAATCTCCAG[A/G]CAGTAGAGCTGTGAG | 9474 |
rs536629133 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244502 | CATGACTCTTTGCCT[A/C]TCTTAAGTTCACCTA | 9474 |
rs536662284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210328 | AGGCAGATAATATAT[A/G]CTATAACAGAGCAAA | 9474 |
rs536686313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106237788 | TCACTGCTTATATAG[C/T]TGGTTAGGATTTCCT | 9474 |
rs536699405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106218025 | TAAGAAAATAGTATA[C/T]ATCAAATATTAATGT | 9474 |
rs536713980 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205862 | AAGTGTTGTTTCTCA[C/T]TTAATGAAAATCTTA | 9474 |
rs536724497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245515 | AGTGACTTAAAATTC[C/G]CTAGCCTCAGTTTCC | 9474 |
rs536770014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252680 | TCTAAAATCCCCCAC[A/G]GGAGACATGGAGGAC | 9474 |
rs536826350 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204393 | GAAAATTGTAATTTT[A/T]AAAAAATCTTGATAA | 9474 |
rs536860008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294748 | CTCAGGAGGCTGAGG[C/T]GGGAGACTCTCTTGA | 9474 |
rs536875188 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261749 | AGTCAATAAATAGGG[A/G]TTTATTTTGGAGGTA | 9474 |
rs536886619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226044 | TCACCTATGGGAAAC[C/G]CTGAGGCTCTGTACA | 9474 |
rs536887527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238952 | CCAATAACTTCATCA[A/G]ACTAGCAAATAACTT | 9474 |
rs536948735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238574 | AAGCTAGAACCTCTA[C/G]AGTGTTTTCCTCTCT | 9474 |
rs536958956 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281932 | ATGACTAAAGATGTT[C/G]AGTGCCTTTTCATGT | 9474 |
rs536981289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273723 | TCCATCTCAAAACAA[A/T]AATTTCTCAGTCTAC | 9474 |
rs537004642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260948 | CAATACAAATGATTT[C/T]TAGGCTTTTGTTTAA | 9474 |
rs537016431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303022 | AGAAATTAAGGTAAG[A/G]GCTCAAAAAAATAAC | 9474 |
rs537024667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203840 | ACACTTAGGCATTAG[C/T]GACAAGGTTTTGTTT | 9474 |
rs537025252 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106311445 | AGTGAAATGAACATG[C/G]GTGAGTGTGGAAGTC | 9474 |
rs537034050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295054 | CCTAAAATTAAAAAA[A/C]AATATACATACACAC | 9474 |
rs537044359 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237236 | GCAAAACTAAACCCA[A/G]TAAGAGGAAAGAAAG | 9474 |
rs537048871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194423 | TGTTTCTTTTTCTAA[C/T]TGCTTCATGTCTGAA | 9474 |
rs537053492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303789 | CTATTATAGCAACCA[A/G]CTAAGGAAGAAAAGT | 9474 |
rs537099141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244778 | GCATGGCAGGCAAAT[A/G]TGTGTGTAAATAAAC | 9474 |
rs537155552 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262934 | CATTTGGGCAGACAC[C/T]GAGCTAGCTGCAGGA | 9474 |
rs537165546 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234931 | AGAGCTTTAGACTTG[C/T]TAACCTCTGAAAGAG | 9474 |
rs537194214 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106301698 | CTTATTGAAGCATTT[C/T]GCATTTCAGATTTTC | 9474 |
rs537206645 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323690 | TCGACCTTTAACCTG[C/G]ATAAATGCAGTCAAT | 9474 |
rs537209140 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188366 | ATCTTCCTCCTACTT[A/G]GCACTGAGTCAAAAA | 9474 |
rs537228068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297240 | AAAGAACATGTGACA[A/G]TATTATTTCATCTTT | 9474 |
rs537228941 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106290951 | GAAATTTTACCACTG[A/C]CAACAAATACTATCA | 9474 |
rs537243611 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288583 | TTCTACAGACAATTA[A/C]CATTAACTTTTAGAT | 9474 |
rs537266020 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106229636 | TAATTGAAGGTCTTC[C/T]CCGCGACCCTATAAC | 9474 |
rs537310761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230978 | GGAAGCCCTCAGAGT[C/G]TACCTCCCTACCCCA | 9474 |
rs537355867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236957 | GCATGTACATCTATA[A/C]ACACATATAAACATA | 9474 |
rs537417927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192209 | TCATTTAATAGACTT[C/T]AGGTAAGGTTATTTT | 9474 |
rs537436425 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298073 | AGGTTCAAGCGATTC[C/T]CCTGCCTCAGCCTCC | 9474 |
rs537452216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199615 | CTAAAAACCAAATTG[C/T]GGTGATGGTTGCACA | 9474 |
rs537454285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106191561 | ACTTCTGTTTCCTCA[C/T]CTTACAGTGTGAACA | 9474 |
rs537475236 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269630 | GACCCAGTACACCCT[C/T]CGCAGCCGCTGGCCC | 9474 |
rs537479053 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324935 | TGGTAAGTCTCCGGG[C/T]TCTGATTGCTCAAGA | 9474 |
rs537486237 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212499 | CAAAAATTAGCCGGG[C/T]GCTGTGGCGGGTGCT | 9474 |
rs537528926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244166 | ATTAGAAAACAAGCA[C/T]TGTTTTATCAGCTTC | 9474 |
rs537556299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251268 | CATACCAACTCTGGC[C/G]TGGCGGGAAGAGGGA | 9474 |
rs537564401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259014 | ATAATCAATTGAAAA[A/T]ATTACTCAGTAACTA | 9474 |
rs537573505 | in-del | -/CCCTAACTCATTTTATGAGG | 0.0244538 | 0.107838 | intron-variant | ATG5 | GRCh38.p7 | 6:106266483 | AAAAGAGGGACTCCT[-/CCCTAACTCATTTTATGAGG]CCCTAACTCATTTTA | 9474 |
rs537585289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106206926 | TAAACGTTGATTTAG[C/T]ATATATAAAATTAGA | 9474 |
rs537590392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198877 | TCTGATAAAGAACTT[A/G]TATCCAGAATATATA | 9474 |
rs537598255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294293 | TTTATCTCAAAATGA[C/G]TAACTCTGACCAAGA | 9474 |
rs537611094 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106273530 | TATGAGGCATTACCA[C/G]CTTCGTATTTGTAAT | 9474 |
rs537617210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106321507 | GGGACTACAGGCGCC[C/T]GCCACCGCGCCAAGC | 9474 |
rs537645474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281894 | TGTAATGTCTCTTTG[C/T]GGTTTTAATTTACAT | 9474 |
rs537647692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272761 | AATCCACACTACTAC[A/G]GTCCGGGCATGATTC | 9474 |
rs537681523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229017 | TACTCAACAGTCGCC[C/T]ATGCGTGCGCTCCTA | 9474 |
rs537724604 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106234832 | TCTCAAGAACTCAAT[C/G]GTGACATGGAATGGG | 9474 |
rs537739634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106188649 | CAACAGAAGCTGGAG[A/G]ACAAAAGCACTATTC | 9474 |
rs537777818 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192975 | CAGCCACGGAGGTAA[A/C/T]AGTCAGCGAGGTCAG | 9474 |
rs537777975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320429 | ATAAAGGTATTAAGT[A/G]GGCAGGTGCAATATA | 9474 |
rs537790531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289237 | TTCTGCCTGAAAATT[A/C]ACACTTACCCAGTTT | 9474 |
rs537791654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285967 | AGTAACTGCCTAGTA[C/T]GTAGCCAGATGTCTC | 9474 |
rs537807088 | in-del | -/GTAAGA | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106188398 | TGAAAGAATAGTGGT[-/GTAAGA]GTAAAAGTTCCTTAT | 9474 |
rs537821738 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106285360 | TATTGAGAGTAAAAT[G/T]TTTTTTTATTTGATA | 9474 |
rs537824958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285291 | AATTTATAATAGTTG[C/G]TTTAATTCATTTTTC | 9474 |
rs537836668 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106305126 | GAATTTTATTCCACA[-/T]TAATTATATGCTTGG | 9474 |
rs537839499 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267129 | CTCCTTAAGCTGTTA[A/C]TAAACTTCAGCAAAG | 9474 |
rs537848611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323173 | CGGTCTCCTGACCTC[A/G]TGATCCGCCCGCCTT | 9474 |
rs537850472 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106275592 | CACTTTAAAATTAAT[G/T]TAATAAAATTTAATA | 9474 |
rs537916924 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106240697 | TCTACCTTTTGATGC[A/G]AAAACTCATTTTTGG | 9474 |
rs537918757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249118 | TCAAATTTTTTAAAT[A/G]AACAACTTGAGATAT | 9474 |
rs537950117 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295709 | GCTGGGACTACAGAC[-/AT]GTGCCACTATGCCCA | 9474 |
rs537982245 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106264247 | AGAAAGGATATCAGA[C/G]ATTGAAGATCAACTT | 9474 |
rs538002385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270504 | AAATGAGGTGGCTCC[A/G]TATTTCATTGCTTTG | 9474 |
rs538023252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106305582 | GTTGTCTCAACTGGC[A/G]ACTAATTTCCTTTCC | 9474 |
rs538032400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213222 | TAATGGATACAAAGA[A/T]AAATAACATGCAAAC | 9474 |
rs538032546 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206514 | AATTAGCTGGGCATA[A/G]TTGTGGGCGCCTGTA | 9474 |
rs538061957 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106306272 | TATTTACCCATAAAC[C/G]TATAAAATATAAGCC | 9474 |
rs538079831 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221758 | AACTTATGTTTACTA[-/T]TATCTACTTATATTC | 9474 |
rs538118265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228528 | CAAGATTCCATTTAT[G/T]GGAATCCATGAGGCC | 9474 |
rs538139144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106242030 | CAAAAGGTGGAAGCA[A/G]CTCCAGCAGATGAAT | 9474 |
rs538153544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242449 | CAGAGAGTTGTTTAA[C/T]GGGTATAGAGTTTGT | 9474 |
rs538154161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312302 | CAAGTAAGAGTAGTT[A/C]TTCTTGCCAAAACAG | 9474 |
rs538169857 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184421 | GTTTGTGACTAAGGA[A/G]ATTTTAATGATTTTA | 9474 |
rs538180386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277421 | ATGCAAGTTAAAACT[A/C]AGCAAAGTGATCTTA | 9474 |
rs538201583 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325911 | ATGCGCCAACGGGGC[A/T]GTACGCTTGAACTCG | 9474 |
rs538212210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198685 | GGGAGGCTGAGTCAC[A/G]AGAATCACTTGAACC | 9474 |
rs538228083 | in-del | -/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326365 | CGGATCACGAGGTCA[-/G]GAGATCGAGACCATC | 9474 |
rs538232123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227547 | GCTGCAGTGAGCTAT[A/G]ACTGTGCCACTGCAC | 9474 |
rs538232275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219970 | CTTATCCCCTCCAAG[C/T]AATATAACAGTGGTT | 9474 |
rs538235515 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320284 | TGGGGCAGGGGAAAG[A/C]GGAGGGGTTGGAGAT | 9474 |
rs538239481 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106237083 | CACATCCACTGTACC[G/T]GAAATAGCCCTACTG | 9474 |
rs538279111 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106226830 | TGAAAAGCACAAAAA[C/T]TGAATTAACTTGAGG | 9474 |
rs538339715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247630 | TGATCAATACATAAC[C/T]TTGTTCTATGTGTGT | 9474 |
rs538371058 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATG5 | GRCh38.p7 | 6:106325460 | CTTCCTACCACACCT[A/G]CCTGGCCCCTCCCCA | 9474 |
rs538371200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190456 | AAGCTTCTAACATGT[C/G]AATTCTGGGGGATAC | 9474 |
rs538385909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205496 | ATTGCATGCTTATAG[C/T]AAAAGATTACATGTA | 9474 |
rs538386838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255165 | CATCTGGGCCAACAT[A/C]TGAGGAGTCCTCCAG | 9474 |
rs538394912 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106212477 | GAACCCGTCTCTAAC[A/C]AAAATACAAAAATTA | 9474 |
rs538430063 | snp | G/T | 0.00199481 | 0.0315187 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184259 | GTTCCTAGTTAACAA[G/T]GCCAATATTTAAAAA | 9474 |
rs538439024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228377 | CGATCCCGACTGGGC[C/T]AAAGACTTGCCATTG | 9474 |
rs538473780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227791 | GCACTGTTCTGGTTA[C/T]TGTCAAGCTATGAGC | 9474 |
rs538496441 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300796 | AAATGCGGTCCATCA[C/T]TGACCAAAATCATGT | 9474 |
rs538511962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233769 | AATCGTAAATCCCCA[C/T]GGCCCTCCCTTATCA | 9474 |
rs538518816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262365 | CACTGCACCCGGCCG[G/T]TCTAGGGTATATTTC | 9474 |
rs538566264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106312733 | GACAATGCCACAAGA[C/T]GGGAGAAGCAACCAA | 9474 |
rs538600885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106292253 | TGGTGGAATCATTGC[C/T]ATTTGAGAATGAATT | 9474 |
rs538617496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324446 | CCCACAGATGCCGAG[A/G]GACAGGAAAGACTGT | 9474 |
rs538619891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283730 | TTCTTAGGTATTTTA[G/T]AGACTTCACCAATGA | 9474 |
rs538622588 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292380 | AAGGGAATGAGGGAC[A/C]AGCACTTCATAAAAT | 9474 |
rs538628234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274711 | TACTTATGAAAAATT[A/G]TTAATATTATTTCCT | 9474 |
rs538632825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192687 | TTCATATTTATATTT[C/T]ATAATTCAGCAGAAA | 9474 |
rs538640217 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236116 | TATGTTCTCTTTGTA[C/T]TGGTTCTTTTTACTC | 9474 |
rs538647684 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATG5 | GRCh38.p7 | 6:106259431 | TCTCAAATTTTTTCA[C/T]TTACAGCTCAGATAT | 9474 |
rs538654378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106283037 | TTCAAGTAATCCTCC[C/T]GGTTCAGCCTCCCAA | 9474 |
rs538715674 | in-del | -/A | 0.0016116 | 0.0283409 | intron-variant | ATG5 | GRCh38.p7 | 6:106192228 | AAGGTTATTTTTTTT[-/A]AAAAAAGATGAAAAC | 9474 |
rs538723672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254994 | AAATACCCTCTATGT[C/G]CCTTTTGCTTCCTCC | 9474 |
rs538775359 | in-del | -/A | 0.19334 | 0.243495 | intron-variant | ATG5 | GRCh38.p7 | 6:106303974 | GCTACTCCAATAAGG[-/A]AAAAAAAAAAAAAGA | 9474 |
rs538780542 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219543 | AACTATTTTCACAGT[A/G]TGTACATGTGTATGA | 9474 |
rs538787643 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326675 | AGGTTTTTCTCTTAA[C/T]TACACGTGCCTTAAC | 9474 |
rs538807217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277259 | TAAAAATTATGGCAG[A/G]TGAAGGTTTTCTTCT | 9474 |
rs538820237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312238 | TAAGTTACCGACTAT[C/T]TGGGATAAGAGAGAA | 9474 |
rs538841630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276412 | GAGCTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 9474 |
rs538854514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304719 | AATTTTGTGAAATTA[A/G]ATATCTTATTATCTT | 9474 |
rs538863454 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217399 | TCATTATAAGGAGTA[A/C]TATGAAATAAAAGTA | 9474 |
rs538905869 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263242 | AGGTCTGGACTGAGC[A/G]GAATTCACCACAGTC | 9474 |
rs538950449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191451 | GTCTCCCAGTTCCAG[G/T]ATCTGGGTCTTTTAC | 9474 |
rs538997963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106267475 | ACTTTCTTTGCAGAA[C/T]TACAAAAAAACTACT | 9474 |
rs539005722 | in-del | -/T | 0.243919 | 0.249926 | intron-variant | ATG5 | GRCh38.p7 | 6:106311832 | AATTTGATCTCCTTC[-/T]TTTTTTTTTTTTTTT | 9474 |
rs539006100 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325944 | ACCAAACCTCTCCAA[A/G]TTCATAGCTTCTACC | 9474 |
rs539027434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106233003 | GCATTAGCCCAAGAC[C/T]TGAGCCGGTTCTCAT | 9474 |
rs539064105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232441 | TTATACACCTGAACA[C/T]AGGAGAACACCCGTT | 9474 |
rs539117851 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272730 | GGCACATAGTAGGTT[A/C]TTATACTGGCTAGCT | 9474 |
rs539126717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235412 | CTATGCCCCAATTCC[A/G]CAGGAAGCAGTTAGA | 9474 |
rs539143869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238187 | TTTACTTTTATTTTT[C/T]AGAGACGGAGTCTTG | 9474 |
rs539148837 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186271 | AAAGGTTTCAGCTTC[A/G]TTATATTTTACAGAA | 9474 |
rs539154367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246326 | TACCCTCCCACTTTC[C/T]ATCTAATTATAGCAC | 9474 |
rs539154678 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106275120 | AGAAGGAAAGCTTCT[C/T]ATAGAAAGTGACAAC | 9474 |
rs539170091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106196923 | AATATAAAATTTCAA[C/G]TAAGCCCTCTTTCCT | 9474 |
rs539206574 | snp | A/G/T | 0.004783 | 0.0487016 | intron-variant | ATG5 | GRCh38.p7 | 6:106321650 | GGCGTGAGCCACCGC[A/G/T]CCTGGCCAACTCTTA | 9474 |
rs539220078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308730 | GCCCAGAATGATCAA[C/T]ACAAATCTATCTACA | 9474 |
rs539237488 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ATG5 | GRCh38.p7 | 6:106208983 | ACCACAATGTGATAT[A/C]ATTACACACCTACCA | 9474 |
rs539276506 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323475 | AGACAGGGTCTCGTT[A/G]TGTCGCCCAGGCTGG | 9474 |
rs539294783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226677 | ATAGAGTATATTCTC[C/T]TTATATCAGCTCTTT | 9474 |
rs539316678 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ATG5 | GRCh38.p7 | 6:106325314 | CCCAAGAGGGACCCC[C/G]CAGGCCACACCCGCC | 9474 |
rs539343553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265239 | TTTAAACCAACAAAG[A/T]TCAAAAAAGACAAAG | 9474 |
rs539345828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322878 | TTAACATATGCAAAA[C/T]GGAAAACCATTTCAG | 9474 |
rs539351427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318625 | TGTATATTTTTTGCA[A/T]GACCTCAAGGGAAGA | 9474 |
rs539360815 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313227 | ATGCAGATAGGTTTT[A/G]CAGATTTGGTGACAG | 9474 |
rs539376196 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106196987 | CAGATAAAACACAAA[G/T]GTATCAAGGGAGACC | 9474 |
rs539388507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315608 | GCTCAGTGAACGTAT[C/T]GTGTGTGTGTATGTG | 9474 |
rs539409386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256118 | AAAGACTGACAAAAA[C/G]ATACCCCCATTATGT | 9474 |
rs539428888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223426 | TTTCAAAAATCCACA[C/T]AGGAAGCAATTTAAG | 9474 |
rs539431322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214203 | TTAAAATTAGCTTAA[G/T]AATGTACACAATATA | 9474 |
rs539467438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229689 | AGCGTAAACAAGGGC[A/G]TAGCCTGAAAACACT | 9474 |
rs539546939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270358 | CTCACGAAGTTGTAG[A/G]TTCTTAAATGCCACA | 9474 |
rs539594079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258274 | CTTGGGAGACTGATA[A/T]GGGAAGACTGATTGC | 9474 |
rs539623585 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ATG5 | GRCh38.p7 | 6:106286129 | CAGGCCTCAGCCAAG[C/T]ACCCAGGGAGAACAT | 9474 |
rs539627520 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106299874 | AATAAATGCCTCCTA[C/T]TCGGAAAGTTGCTGC | 9474 |
rs539627620 | in-del | -/ATT | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106296374 | AGAACTTATTTCATC[-/ATT]ATTTGTCAATTATTC | 9474 |
rs539665453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293481 | TTACTTTTAGAACTT[A/G]AAATTTTAAAAAACT | 9474 |
rs539691704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250208 | ACCTGTTTGAATCCA[A/G]TCTACTGGCAATCTA | 9474 |
rs539697015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223853 | CTGTTGGCTCTGCCA[C/T]CAAACAATAAGCTAA | 9474 |
rs539718672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315112 | TACCCAAAAAGTGAG[C/T]GAATGGGCTCCTTAA | 9474 |
rs539732265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249526 | AGTTTCCGCTTTTTA[A/T]CTATTATAAATAATG | 9474 |
rs539745227 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227236 | TTCAGATTAATAACA[A/G]ATTTCTCATCAGAAA | 9474 |
rs539812360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314182 | TTTCCAATTTAAACA[A/G]GTCTATAAAGAAAAA | 9474 |
rs539818382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207302 | ATATAGCTCAGAGAT[A/G]TATTGAAGAAAAGCA | 9474 |
rs539839314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213483 | CAAAAGAAGATAAAA[A/G]TAATGGAGGGAATAT | 9474 |
rs539855139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106277491 | AAAAAATTTTGTCAA[A/G]ACATTAAAAACTCTT | 9474 |
rs539877686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228567 | CAGGTCAGAGAACAC[A/G]AGGCTTGCCATCATC | 9474 |
rs539919978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106263068 | GGGTCCCACTCCTAC[A/G]GAGCCCAGCAAGCTA | 9474 |
rs539921996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320339 | ATAATTTTAAAAGAT[A/G]TGGAACTTGAAGAAT | 9474 |
rs539925382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106267231 | CAAATCATGAGTGAA[C/T]TCCCATTCACAATTG | 9474 |
rs539956341 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106269540 | GGCTGCAGGTCCCGA[A/G]CCCTGCCCCGCGGGA | 9474 |
rs539971698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313404 | ATACATAAACGGATC[A/G]CTGCCTAATGTTAAG | 9474 |
rs539973549 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278719 | AATTCCCTTTTTTCA[A/T]TTATCCATTTTTATA | 9474 |
rs539977509 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326801 | TTTAAAAAGAAAAAT[C/T]TTCTTGGAGTTGGAC | 9474 |
rs540003922 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106201246 | GTATGTATTATACAC[A/C]TATGTATATCTCAAG | 9474 |
rs540007190 | snp | A/G | 0.000298166 | 0.0122063 | intron-variant | ATG5 | GRCh38.p7 | 6:106292996 | TATTATGTATCACAA[A/G]TGGGACGAAGGAGAA | 9474 |
rs540020598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307145 | CTCTCCTTGCTAATA[A/T]ATAGTCCTTTGATTC | 9474 |
rs540032420 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258324 | GCTGCAGTGAGCCAT[A/G]ACCTTACCACTGCAT | 9474 |
rs540034366 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230023 | GGGATTTAAATCTTA[A/C]TTACCATACAAAGGT | 9474 |
rs540038720 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106200439 | GATTTAAAGTTTTTT[A/T]AAAAAAATTTCTATT | 9474 |
rs540053422 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106207535 | GAGAGACCTCATCTC[C/T]TAAAAAAAAAAGAAA | 9474 |
rs540091094 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106213676 | TTGGAATGTCAAATG[C/T]AGTGGAAATAACAAA | 9474 |
rs540133364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313662 | ATATAGGATATAGGC[A/G]GAAAGATTATGCACA | 9474 |
rs540164484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314414 | ATCTAAAAATTAACC[A/G]AGCATGATGGCACAT | 9474 |
rs540238624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106297771 | ACACACACACATATA[C/T]ATTTTAAAGTTCATT | 9474 |
rs540239846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269200 | GTTACAGAGTGTCGA[C/T]TGGTGCATTCACAAA | 9474 |
rs540252018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221259 | ACATTTTGTAATATT[G/T]TCTTCTAAGAGCTGT | 9474 |
rs540264542 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190221 | AAACATTTATTTCTC[A/C]CAGTTCTGGAGGCTG | 9474 |
rs540287026 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234704 | ATGTTGTACCTAAGC[C/T]CCACAACAAAAGAGT | 9474 |
rs540295603 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106239249 | TGGAAACAAAATAAA[A/G]AAAAACAAAATCTAC | 9474 |
rs540309699 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326391 | CCATCATGGCTAACA[C/T]GGTGAAACCCCGTCT | 9474 |
rs540335891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233848 | CCCTCCATGCTGCTG[C/T]ACAACCAGCAGCTCC | 9474 |
rs540362683 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106311959 | CCTCAGTCTCCCAGG[A/T]AGCTGGGATTACAGG | 9474 |
rs540367288 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106276767 | CTTCTCTCTTTACAC[A/G]ATCCTCATCTTTTTC | 9474 |
rs540378641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226909 | AAGATAGGTCAATTG[A/C]GAGAAAGAGAGGGAA | 9474 |
rs540381364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249344 | ATATAAATGAAGTAA[C/T]ATAATATGTGGTTCT | 9474 |
rs540386265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256986 | ACAAACACGTACAGC[C/T]GCATAAAAACATTTT | 9474 |
rs540391500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299047 | GTAACCATTGGCTAT[G/T]ATGTTGCTACTTCTA | 9474 |
rs540411326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191570 | TCCTCATCTTACAGT[A/G]TGAACAAAGAATTCT | 9474 |
rs540415799 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325609 | GGTGGGGCGGCGGGG[C/T]AAGCTGCCCGCCTGA | 9474 |
rs540421432 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106195520 | TTTTAATACGTAATA[A/C]AAAGAAGAAGCAAAG | 9474 |
rs540429872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303590 | ACCCTAATGCTAAAT[A/C]AGACAATAGAAAAAA | 9474 |
rs540446934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106291902 | GTGCAAAGCACATTA[C/T]AATAAATGTACACGG | 9474 |
rs540458533 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106197529 | TATTTGGGTTGGGGT[C/G/T]GGGGGGGCGGGGGTG | 9474 |
rs540483044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291427 | CATTATCAGTGTAAA[C/T]GTTAACACAACGGGA | 9474 |
rs540494606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106198923 | TGAGTAATAAGGAAA[C/T]AATCCATGAAAAAAA | 9474 |
rs540520375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256405 | GCAGGACCCACTCCA[A/G]ACCAATTACCTGATT | 9474 |
rs540527607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263903 | AAAAAACAGCACAAA[A/G]ATGCTGAAGATTCAA | 9474 |
rs540545528 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247507 | GTAAATTCTTGTGAT[C/T]TGCAGTAGTTCTGTT | 9474 |
rs540612294 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106298242 | GGGATTACAGTCATG[C/G]GCCACTGCACCCAGC | 9474 |
rs540645806 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305633 | TCCGAAGAATAAATA[C/T]AGGAAGGACGTTATT | 9474 |
rs540663573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212165 | GATGGACTCTGGAAA[C/T]ATCAAGAAGTGAAAA | 9474 |
rs540671325 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106197789 | TGAGTTAAATAAACC[-/T]TTTTTTCTTTATAAA | 9474 |
rs540690245 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299248 | ATTCTCCCGTATACT[A/T]TAAATTATTGCTAGA | 9474 |
rs540702407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211507 | TGAGGTCGGGAGTTC[A/G]AGGCCAGCCTGGCCA | 9474 |
rs540725913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258601 | GAGAGGAGAAAATTG[C/T]AGCTCAAAGCAGCTA | 9474 |
rs540762868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257904 | GTAGGACCTGTGTAG[A/C]GTGAAATCTATCAAA | 9474 |
rs540811952 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199064 | GAGATACCACTAGGA[C/T]GGCAATACATGTGAC | 9474 |
rs540813514 | in-del | -/GTA | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106282333 | AATGCCATATTTATT[-/GTA]GTATTTATGCATTTC | 9474 |
rs540846189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288704 | CTCTCTGAATCCAAC[A/C]CAATGCTGCAGAATC | 9474 |
rs540850232 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254199 | GTCTCAATAGTGTTA[C/G]CCCCTCAGAAAGATT | 9474 |
rs540868452 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106187595 | TCAAAATACAATGTC[G/T]AAACCTCTCAGCTTC | 9474 |
rs540879418 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237885 | AAAGACATAAGCACA[G/T]TACAGAGCCTTAGCT | 9474 |
rs540887090 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307999 | ACTTAAGGTAATCAT[A/G]TATATAAAGATGTTA | 9474 |
rs540931164 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250482 | AGAATCTTGGTCTTC[C/T]GATTCAAAGTCCCCA | 9474 |
rs540943404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247736 | AAAATGTAAAAGCAT[G/T]GCACTACATACACTG | 9474 |
rs540990998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244364 | CCATTCTTTACAGGA[C/T]ACAGAGAAAACTCGT | 9474 |
rs541006155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202877 | CATGTTGCCCAGGCT[C/G]GTCTCAAACTCCTGA | 9474 |
rs541006403 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106314222 | TCTTTACATGAAATT[-/TC]TCTAACTTTAGGAAG | 9474 |
rs541009778 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184647 | TGGTACAATAATGAA[C/T]GAGGAAGTAAAAATG | 9474 |
rs541041024 | in-del | -/AAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322098 | AACTGTCTTGGAAAT[-/AAAG]AAACTCCAACCTGTG | 9474 |
rs541074405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216466 | AATGAACCTTAAAAA[C/T]AATATGCAAGCAAAA | 9474 |
rs541075386 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224615 | GTGCGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 9474 |
rs541079841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106208734 | AAGAGAATGAAAACA[C/T]AAGCCGCAGGCTGGG | 9474 |
rs541091145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106193298 | GAACATGCAATATCA[C/T]AGTATATACCAAATA | 9474 |
rs541124815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308272 | AATGACTTCTATCCT[C/T]GCAGGACTTTTTTTA | 9474 |
rs541127861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200741 | CGCCTTGGCCTCCCA[A/C]AGTGCTAGGATTACG | 9474 |
rs541136005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106228611 | GCCACCATCTTCGGA[A/G]TTCTGGGAGCAAGGA | 9474 |
rs541161627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309065 | GTGTTTTGGAAAATC[A/C]ATTATGATTTATATA | 9474 |
rs541184535 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106188453 | GCCAGTCACCTTTGT[A/G]TACTATGAAACAGCA | 9474 |
rs541187284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249663 | ACTGATACATGGTAA[C/G]TGTGTTTTGAGGAAC | 9474 |
rs541197449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106264807 | CTAAGGGATTTTGTC[A/G]TCACCAGGCCTGCCC | 9474 |
rs541211012 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217165 | AACAAAGATCAGAGA[C/T]ACATTTCTACCTTAT | 9474 |
rs541222585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195266 | ACAATGGTGCCACAT[A/G]ACTTTTATGAAGTAC | 9474 |
rs541256470 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215717 | ATGGTTTCTTACATA[C/G/T]GGCAACCTAAAAATA | 9474 |
rs541274250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106237274 | GTATTTCTTTAATCC[C/T]TTAAAATTCAAATCA | 9474 |
rs541274329 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257035 | AAACTTATTTAAAAA[C/T]TTATTTTTTTAACTT | 9474 |
rs541274417 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191018 | ACAAAGGGCTCTGAG[C/T]AGGTCTCACGTCACT | 9474 |
rs541274509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271547 | AAAATAATCAGACGT[C/G]TTCCCTAATCACCTT | 9474 |
rs541292930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229860 | TCATTGTGAGCACAC[C/T]TCACCGGTTCAGAAT | 9474 |
rs541294915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106223512 | CTTGCTGTGTTGGGC[C/T]GCCCCCTACAGGACT | 9474 |
rs541304170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244987 | TCATTAATCACCACC[C/T]GTTTACAAGTGCTAA | 9474 |
rs541318127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236377 | GATCAGAAAGTAAGC[A/G]TATGTTGAATTTTGA | 9474 |
rs541325566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265514 | GGACCTAATAGACAT[A/C]AACAGAACTCTCCAT | 9474 |
rs541360067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295168 | AATTGAACAAGCTCT[A/G]AATAATACCTTATAC | 9474 |
rs541384909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322340 | CTGAAGTAATTTTCA[A/C]TGACAAAACCCCCAA | 9474 |
rs541405289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106279198 | CTTAGCTTTTTCCTT[C/G]GGAGTATTTTCTAAA | 9474 |
rs541420051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287070 | TAACTAATACAACAT[A/G]CTATTGATAGATACT | 9474 |
rs541424105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308189 | ATGCATCCAAACAGA[A/C]GGCAGAAATATTTTC | 9474 |
rs541427098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264699 | ATATTCAACATTCTT[A/G]AAGAAAAGAATTTTC | 9474 |
rs541427733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257722 | ATTTAGTAAGCCTAA[A/T]AAGCTCCTCCATTCT | 9474 |
rs541430690 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205043 | TCACTCAGGGTTTTT[G/T]ATCTTCAGGCCATGA | 9474 |
rs541527524 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230698 | AAAACACCCCTAAGA[C/T]GTATTCTGGAGAATT | 9474 |
rs541555387 | in-del | -/ACAGTA | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106222816 | AGGTATATAAAGGGG[-/ACAGTA]ACAGCATTTAACCCA | 9474 |
rs541558447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264026 | GAAGGCTTCAGAAGG[G/T]GGGTAATAACAAACT | 9474 |
rs541564369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271519 | TCTTGGACTCTCTAG[C/T]CGCTAGATTGTGAAA | 9474 |
rs541574546 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106322999 | ATCTCGGCTCTCTGC[A/C]AGCTCTGCCTCCCGG | 9474 |
rs541596265 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106315331 | CCTGAGACACAAAAA[A/G]AAAAAACAGTAACGA | 9474 |
rs541607148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224065 | TGGGGCATATGTGAA[G/T]AAATCAAGGAAGACT | 9474 |
rs541643585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194197 | GAAATTGTAAAACCC[A/G]CAATCTGATGAGGTT | 9474 |
rs541645034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287970 | TTCACTGGACCACAA[C/T]TAACTTTTTTTTTTT | 9474 |
rs541646082 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304764 | CTACACAACTGTACA[C/T]AATTGTTTGAAAACT | 9474 |
rs541761362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293842 | ATTTCAATGGACAAA[C/T]CTTAAGTCATCCTTT | 9474 |
rs541763064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106301190 | ACTCTATTTTGAGTT[A/G]GGCCAGCACTTTCCA | 9474 |
rs541847427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106208052 | AGCCGAAATCGCGCC[A/G]CTGCACTCTAGCCTG | 9474 |
rs541863793 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207331 | CAGAAAAACGAAACT[C/T]ATAAACATTTTAGGA | 9474 |
rs541899030 | in-del | -/GT | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106315609 | CTCAGTGAACGTATC[-/GT]GTGTGTGTATGTGTG | 9474 |
rs541902617 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106314568 | TCTCAAAATAAATAA[A/T]AAATAAATAAATAAA | 9474 |
rs541912240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249327 | CCTATTCCAGACATT[A/T]CATATAAATGAAGTA | 9474 |
rs541921365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223470 | AGTCTCAATCTCAGC[A/G]TAGTAGATAGCTTAG | 9474 |
rs541939938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322281 | ACAATATAATGCATA[A/G]TAGTTTCTTTCACAC | 9474 |
rs541989434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256255 | TAATGATTATCCACT[A/G]ACAAATAACACAAGC | 9474 |
rs541992122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270966 | CTCTCCCAACATCAC[C/T]CTAAATATCACCATA | 9474 |
rs542029486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287353 | ACCAATGCAGGGCTT[C/T]TTCAAGCATGGTAAG | 9474 |
rs542064981 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185866 | ACAGAGTAAAAAGTG[A/T]TCTACTGTATGTGAG | 9474 |
rs542068485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106209225 | AACTTATACATGAAC[A/G]TTCATAGCTGTTTTA | 9474 |
rs542098818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251357 | CCTTTGCAGGTGGGA[C/T]CCCTTACAAGTTTGG | 9474 |
rs542108871 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106325107 | CACTAAATATTGTTA[C/T]TGAGACAGGGAATAT | 9474 |
rs542143227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106235075 | CGAGATTGAATACAA[C/T]GTAGAACAGAGGAGC | 9474 |
rs542194731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285643 | TTAACACTGTGCAGG[C/T]CATACAGTCTCTATC | 9474 |
rs542200194 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106188508 | TCCAAAGTACTGTAT[C/T]TAAAGCAATATTTAA | 9474 |
rs542233556 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228440 | AATTGAGCTGAACAC[C/T]AGTCACTGGGTTCCA | 9474 |
rs542256496 | snp | C/T | 0.000264166 | 0.0114897 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293097 | AAATAGCAAACCAAT[C/T]GGATAATGCCTAAAA | 9474 |
rs542358158 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311991 | GTCCACCACCACACC[A/G]GGCTAATTTTTTGTA | 9474 |
rs542408286 | in-del | -/T | 0.155325 | 0.23138 | intron-variant | ATG5 | GRCh38.p7 | 6:106194545 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTTGAGAT | 9474 |
rs542409280 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325639 | ACACACTGTCCTGCG[A/G]GGACGCGGTAGCAGG | 9474 |
rs542433411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275885 | TGTGGGCCACATAGT[A/C]TCCTCATAATGATTT | 9474 |
rs542494998 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184113 | TATCCTTACATAACT[C/T]AAATATTGCTATTTT | 9474 |
rs542515980 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326969 | TATTGTGTCCCAAAA[C/T]TTTTACTTCAGTATG | 9474 |
rs542516264 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233321 | ATTCCCAGGTACGGC[A/G]AAATAGCCAGACCAT | 9474 |
rs542530807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239153 | CTATAATAGCAATGC[A/T]ATAAAGCAAGAAAAA | 9474 |
rs542531098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106234457 | CAATCTGGAAATAAC[C/T]CATACCTCAAACCTC | 9474 |
rs542558729 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262015 | GGTTCCCAAACTTTA[G/T]TGAGTCAAAACCTTC | 9474 |
rs542563566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323246 | TCTTTTCCGTTTCGC[A/T]AAGTGGAAAAGTCCT | 9474 |
rs542567440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106316076 | CAAGGTTAAATATCC[C/T]ATTTGCCACAATCAA | 9474 |
rs542567718 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186280 | AGCTTCATTATATTT[A/T]ACAGAAGACCTTCAG | 9474 |
rs542589810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106193218 | CAGAAAAATACAAAC[C/T]CATTTAAAAATACTT | 9474 |
rs542601506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274125 | TGGGATTGTATACTC[C/T]GAAAAGCAAGAAACT | 9474 |
rs542619054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188386 | TGAGTCAAAAAATGA[A/G]AGAATAGTGGTGTAA | 9474 |
rs542622594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106296679 | AAAAATTAGCTGGGC[A/G]TGGTCGCATGTGTCT | 9474 |
rs542630670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290406 | GCTCACTCCAGCCTC[A/G]AATTCCTGGGCTAAA | 9474 |
rs542665821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289884 | TATGTTCAATATTCT[A/G]CAATATGTTGTTTTG | 9474 |
rs542699748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224339 | AGAAGATAAAGGACC[C/T]ATGAGCTAAATCAGT | 9474 |
rs542706544 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310872 | GTTCTTTTACTTTGA[A/G]TAAGATTAACCACAT | 9474 |
rs542727372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323066 | TGGGACTACAAGCGC[C/T]TGCCACCAGGCTCGG | 9474 |
rs542727807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252998 | TTATTCAAATCAGTA[C/T]TACAAGTGATCATGT | 9474 |
rs542736856 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106230528 | GAGCATAACTAATCC[A/G]ATAAGCAGAGGTCCA | 9474 |
rs542758272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187538 | AGAAACTTTGTGTTA[C/T]TCCTTTAGCACAATT | 9474 |
rs542786023 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106296031 | AAAGTACATAATAAA[C/T]AACTGCTGAATGCAT | 9474 |
rs542798263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318281 | AAACATCATGCATGT[A/G]AGTGTGGCTCCCTTC | 9474 |
rs542800800 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296569 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCTG | 9474 |
rs542801809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280461 | TTTGACTAGGTTAAG[C/G]TTACTATAAGTCAAT | 9474 |
rs542807081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210371 | AATGTATAAATCTTA[C/T]AAGAACCAAAATCAG | 9474 |
rs542819737 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106274948 | CAAAAGGTCATGAAA[C/G]TTGAAAGCATTAACA | 9474 |
rs542845945 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106218108 | ACTTTGGTAAGGGGT[C/T]GAGTAAGGAGCATTC | 9474 |
rs542852473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226325 | CAGACCTTGGGAAAG[C/G]GGGGAAGCATCTGGT | 9474 |
rs542871217 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260201 | AACATGGCACATGTA[C/T]ACTTATGTAACAAAC | 9474 |
rs542889364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232771 | CACTGTCCCTCTATA[C/T]CTAGCTGTACCTAAC | 9474 |
rs542906218 | in-del | -/A | 0.157642 | 0.232314 | intron-variant | ATG5 | GRCh38.p7 | 6:106221686 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9474 |
rs542921836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216795 | AGGCAAGAGGATCAC[C/T]TGAGCCAGGAGTTCC | 9474 |
rs542929040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324114 | CTTTCCGCCACTTGA[C/T]GTACACAGTTGGCCC | 9474 |
rs542956761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283461 | AGTGCAGTGGCTACT[C/T]ACAGGTGCACTCCCA | 9474 |
rs543015196 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106272924 | AAAACTCACACAGAC[A/G]AGGAATGAAAAATAA | 9474 |
rs543024895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295224 | CTTCAATTTATTTTT[C/T]AGAATATCTCTCTTA | 9474 |
rs543029031 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280042 | TGTTTTATAACAACA[C/T]GAAAAAAAGGCATCA | 9474 |
rs543054754 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106231046 | CCCTTCAACCCAAAC[A/G]GTCCAAAAGGAGATA | 9474 |
rs543211227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303157 | TAAAAAGGAGAGAAA[A/C]ATCCATGAACCACAA | 9474 |
rs543230838 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266968 | GCCCTCTCTCACCAC[C/T]CCTATTCAACATAGT | 9474 |
rs543238915 | in-del | -/AGAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301381 | TTGATATAAGCAATT[-/AGAG]AGAACAGATAAGATG | 9474 |
rs543314230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224805 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 9474 |
rs543325757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245700 | TTTCAGTAAAAATTA[C/T]GCCCTTTATTAATGA | 9474 |
rs543337606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106231140 | GTGGGAGGAGAATTC[A/G]GCCCAGCCAGAGTGC | 9474 |
rs543391717 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248775 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAATT | 9474 |
rs543405190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209788 | ACTAGATGAAGGGTA[C/T]GTAGATCTTTCTGTA | 9474 |
rs543416695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295970 | AAACGAGAAAACTAT[A/G]AATATTTTAAAAATG | 9474 |
rs543438169 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106262264 | AGAGATGGGGTTTCA[A/C]CACGTTGGTCAGGCT | 9474 |
rs543456136 | snp | C/T | 0.000364673 | 0.0134983 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186539 | GCAAATAGTTGATCC[C/T]TCAATCTGTTGGCTG | 9474 |
rs543457664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209820 | TATTTCTTACAATTG[C/T]ATGTGAATCTGTAAT | 9474 |
rs543459158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106203331 | GAGCCAGTGTCTATG[A/G]AGAGCACCACTGTTT | 9474 |
rs543460640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229900 | TCAAAAAAGCAAAAA[C/G]GTAGCTTATTAACTC | 9474 |
rs543496942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202943 | GTTAGGGTTACAGGC[A/G]TGAGCCAACCGCTCC | 9474 |
rs543530669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259433 | TCAAATTTTTTCATT[C/T]ACAGCTCAGATATCT | 9474 |
rs543541825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301302 | TCGACAACAACAAAT[A/G]TATTGAGTATTCATT | 9474 |
rs543552481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194118 | CCCAAATCAAATAGC[A/G]TGAAGGTACAGAGAT | 9474 |
rs543580339 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295565 | ATAAAATCAAGTAAT[-/T]TTTTTTTTTTTTTTT | 9474 |
rs543580650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106302172 | CTACAGGAGGGAATA[C/T]ATGAATGAATAATTA | 9474 |
rs543597027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324001 | CCCTTCTTTATCACC[C/T]GTAGGCCTCCAAGTT | 9474 |
rs543645097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209361 | AATAAAAAGGAACAA[A/T]CTACTGGTATATGCA | 9474 |
rs543652920 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212471 | TATGGTGAACCCGTC[C/T]CTAACAAAAATACAA | 9474 |
rs543654709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289659 | ACTAGAAATTAGAGC[G/T]GAAACATTTAAAAAA | 9474 |
rs543669020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106283491 | AGTACTAATCAGCAC[A/G]GGAGTTTTGACCTGC | 9474 |
rs543682055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216612 | CTGCCAATGGGCATG[G/T]GGTTTCTTTTTAGGG | 9474 |
rs543706726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230414 | AGCACAAAGGCAATG[C/T]TGGGCACGCTGGTAA | 9474 |
rs543743704 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185248 | TCAGCATTTGTATAA[C/T]TTTTTATAAGAAAAA | 9474 |
rs543752850 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316491 | CAAAATTACATATGC[C/T]AGTAATATTCATTGC | 9474 |
rs543760998 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326271 | GTACATATCTTTATC[G/T]TACTCTTTGTAAAAA | 9474 |
rs543764362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187512 | AAAAGAAAAAAAAAA[C/T]AGAACCATCAAGAAA | 9474 |
rs543782154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315910 | ATGCTGACAGTGGTT[C/T]TGTCCTCTGAGTGGT | 9474 |
rs543816636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287899 | ATACAGAGAGAAAAC[G/T]CAAAGGTGGCAAAAT | 9474 |
rs543846719 | in-del | -/TC | 0.00755907 | 0.0610114 | intron-variant | ATG5 | GRCh38.p7 | 6:106221989 | GTCTGCCTTCCAGGT[-/TC]AAGCAATCCTTGTGC | 9474 |
rs543852298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227134 | GAATAAAATCAAAGC[A/G]ATCCACACCTAGGTA | 9474 |
rs543852964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106279332 | CCCAGAATTTTCCAC[C/T]GTGACCACAGAAGGG | 9474 |
rs543911961 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207843 | TCATGCCTGTAATTC[C/T]AGCACTTTGGGAGGC | 9474 |
rs543918822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233782 | CATGGCCCTCCCTTA[C/T]CATATTTTTCTCTTT | 9474 |
rs543925097 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199663 | AAAAATCATTAAATT[A/C]TAAAAAAATTATTTA | 9474 |
rs543946078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190739 | GGTAAGAATTACATA[C/T]AGAAAAAAAATAAGA | 9474 |
rs543986170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217266 | GGAATTTAAATAACT[C/T]TGTCTTAACTGTTCA | 9474 |
rs543995289 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212103 | TTAGATTTGCCTAAC[C/T]ATATAAGTAGTACTA | 9474 |
rs544000210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213648 | GTGGACTAAAGGCCA[G/T]AGCATATAGAGCTTG | 9474 |
rs544005225 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203904 | TTTGACACAACTGTT[-/A]AGAGATTTGGTTTAA | 9474 |
rs544028628 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189802 | AATGTCACTACAAAG[A/C]AAATGACTCAGGAGA | 9474 |
rs544031976 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106243160 | ATAGAAGTTAAATAG[A/T]TTTGCTTAACCAAAA | 9474 |
rs544044720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106263157 | GATCAAGCTTGGTGC[A/G]GGGAGGGGCATCTGA | 9474 |
rs544089741 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106319728 | TTTATTTGTACGTCT[C/T]CTCCAGCAGACTGTA | 9474 |
rs544094024 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319820 | TGGTATCTGGAATTC[A/G]GTAGGTGCTCAAAAA | 9474 |
rs544111320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220352 | TGCATGCACTGCAAA[C/G]CAAAAGTATAATATA | 9474 |
rs544166184 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297443 | CTGGCAAAGGGTTTA[C/T]AGATTTCTTCAAGTA | 9474 |
rs544170093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272235 | TTCTAATTCATTAAC[C/T]ATACTGCAGCCAAAG | 9474 |
rs544204406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276517 | TGACTTGACCTAAGG[A/T]CTACTAAGACCTGAA | 9474 |
rs544206029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106268431 | TTACACTGTTGGTGC[A/G]AGTGTAAATTAGTTC | 9474 |
rs544220589 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238676 | ACAGAGAGAAGACCA[-/G]GGAACAAAGAGACTT | 9474 |
rs544297872 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106187456 | TATAAAGATTTTTGT[-/C]ATAGAAAAACAAAGA | 9474 |
rs544310463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239976 | GACACCTATCTCACA[A/C]AACACATTGTGGGAA | 9474 |
rs544316391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210660 | ACGATGGATTCAGCT[C/T]ATGGTTCCAATCCCA | 9474 |
rs544327734 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277362 | ACAGGAATTACAGGA[C/T]ATGCCCTCACTTTGC | 9474 |
rs544369796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317725 | TACAAATTCAAACTA[C/T]TGAGTTTCTGCATTT | 9474 |
rs544379074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198105 | AAAACAAACACCCTT[A/G]TAACAGAGAAAATGA | 9474 |
rs544387125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305888 | AGCAAAGAGAGAAAA[C/G]ATCAAGACTAAGCCC | 9474 |
rs544390158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106206627 | TGAACTCCAGCCTGG[A/G]CAACAAGAGGGAAAC | 9474 |
rs544390627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246833 | TTACTGTGGAGCTCA[A/T]GGTAAAATAGAAAGA | 9474 |
rs544433121 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106239245 | GAAATGGAAACAAAA[A/T]AAAGAAAAACAAAAT | 9474 |
rs544496287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205570 | ACTAAAAGATTAAAA[A/C]TTACCTGAAAAAAAA | 9474 |
rs544504586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290615 | AGGTATCATGCCCAT[A/C]CAGTTTATTGTAATA | 9474 |
rs544509223 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187229 | ATTTGAATAACAGTT[-/A]AAATTTTAATGAGAA | 9474 |
rs544556894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269159 | TGTCGACACAAAGGT[C/T]CTCCAAGTCCCCACC | 9474 |
rs544562541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261203 | CATTATTTCAAAAAA[C/T]GTAAGCAGAATGTCT | 9474 |
rs544591230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211452 | GTGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 9474 |
rs544652980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219392 | ACATTAACTCAGCCA[C/T]ACATCTAACACAGTC | 9474 |
rs544710198 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292758 | TACAGGCGTGAGCCA[C/T]CAAGGCTGGCCCAAA | 9474 |
rs544723348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106325015 | TAGGTTCCTCAAGTT[A/C]AGGATAATTTTAAAA | 9474 |
rs544730588 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225615 | AGGACCCTGAATATA[A/C/T]TCTCCTCCATAAAAG | 9474 |
rs544733379 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315870 | ACATGTAAGGAAAAC[A/G]AAGTCCAGAACGCAT | 9474 |
rs544779646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106291315 | TCTTTTTACTCTAAG[C/T]GTGTGGTTATAAAGA | 9474 |
rs544838886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319661 | GAACTCGCCTTGTTT[A/T]CTCTTGGCACCTCTA | 9474 |
rs544842932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269028 | TTCTGCACATGTATC[C/T]TAGAACTTAAAGTAA | 9474 |
rs544849985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204962 | GTAAAGATAATAAGG[C/T]TGAGGAGTTCAGAGA | 9474 |
rs544865298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220902 | CGACATTCTCTATGA[C/T]GGAAAGGGACTGAAA | 9474 |
rs544891091 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273012 | GATTCATTCTACTAT[A/T]TTCTTTGCTCTTATT | 9474 |
rs544906173 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226436 | GTATAAGCCACAAAC[G/T]GGGGGGAAAAAGCAG | 9474 |
rs544909078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254340 | TAAGTATGTACTGTC[A/G]CTCTCCCTCAACCAA | 9474 |
rs544912878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246871 | TAATTAAAATAAAAT[A/T]GACAAATGATAAATG | 9474 |
rs544989703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190028 | TACATAACTACAGTA[C/T]AGTTATCACAATAAA | 9474 |
rs545002680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106284052 | GTAAGGATACATACA[A/G]TATTTTGTTTATTCA | 9474 |
rs545074236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239195 | AAAAACACAATAGGA[G/T]GAGATTTTTGTTTTT | 9474 |
rs545077596 | in-del | -/A | 0.4628 | 0.13121 | intron-variant | ATG5 | GRCh38.p7 | 6:106198777 | GAGACCCTGTCTGGG[-/A]AAAAAAAAAAGAGAG | 9474 |
rs545079739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290518 | TAGAGATGGGGTCTA[C/T]GTTGCCCAGGCTGGT | 9474 |
rs545081351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266202 | TACAAACCACCATCA[A/G]AGAATATTATAAACA | 9474 |
rs545081797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106287499 | ATTTTACTTAACAAA[C/T]GTGAGCTCTTACCCT | 9474 |
rs545111167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246768 | ATTTTCTTCAACTAA[A/G]TTATACAAGTAAGAT | 9474 |
rs545117816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316732 | CAAAACTACTCTCCC[A/G]TCTTAGAAAATATCT | 9474 |
rs545129516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197094 | AGATCATTACAGAAC[A/G]CATTACTTCCAAAGT | 9474 |
rs545133878 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ATG5 | GRCh38.p7 | 6:106209387 | ATGCAACAACTTGGA[C/T]AGATCTCAAGGGAGT | 9474 |
rs545159627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323331 | ATGGACTACAGTGAA[A/G]GATCATGGGTCACTG | 9474 |
rs545169613 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289641 | TATATTACTGATATT[C/T]ACACTAGAAATTAGA | 9474 |
rs545171433 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260588 | TTCATAAGTTGCTTA[-/T]TTTTTTCCAGTGTTT | 9474 |
rs545178982 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270603 | CAGTACGAAACTAGA[-/T]AGCTGCAGCATTAGA | 9474 |
rs545213691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106220235 | TTCAAGTATGCATAT[A/G]TCAATATCTGTATCA | 9474 |
rs545214151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211368 | GGAGTCTCCTACGGA[C/G]ACAGCAGGCAGAATG | 9474 |
rs545252596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210545 | TTTCCAAAACTGACC[C/G]TTCGTATTTCAAATA | 9474 |
rs545270454 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325700 | CACCGGCGCGGAGGT[C/T]GGAGCTGAACCCTGC | 9474 |
rs545291417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310714 | CCCCATTCCCTGCTT[C/T]CCCAGCTCCCAGTAA | 9474 |
rs545295207 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210695 | TGTCAATTAGTACCT[A/G]TATGACCCTAGTCAA | 9474 |
rs545333951 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296684 | TTAGCTGGGCGTGGT[C/T]GCATGTGTCTGTAGT | 9474 |
rs545357236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266867 | CAAAATAGTAAGAGC[A/T]ATTTATGACAAACCC | 9474 |
rs545378820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218261 | AACTATCAACCAAAC[G/T]ATAGAAAAGAGTGCA | 9474 |
rs545381900 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212059 | ACTGGAATTAGCAAA[C/G]TTCATTTATTGATTA | 9474 |
rs545388884 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106274165 | TAAAAACATTTTTTA[A/T]AGATTTCCTCAAATC | 9474 |
rs545392962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273787 | GGCAATGCAATGACA[A/G]CCCACCAGTCTATAT | 9474 |
rs545415096 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ATG5 | GRCh38.p7 | 6:106225443 | ATATACTGAGTTGAA[A/T]TTTTTATATTTTATA | 9474 |
rs545420185 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ATG5 | GRCh38.p7 | 6:106296540 | ATAAGCATGCAGGCT[A/G]GGCGTGGTGGCTCAC | 9474 |
rs545464648 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243115 | TTCTCTCCCCAAACC[A/G]GTATCTAGATTCTTA | 9474 |
rs545470130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214617 | TTTGTCTTATTTAAA[C/T]TGTTATACTTATTAT | 9474 |
rs545480184 | in-del | -/ATTAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193540 | TAAAAAGCAAAGTGT[-/ATTAA]ATTAAGTGATTGTAA | 9474 |
rs545516976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313859 | ATTTTCTTCCTTGTA[C/T]GTATTAACTTACACT | 9474 |
rs545521786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231104 | AATGCCAATATTCCC[C/T]GATTATGCCCCCTCC | 9474 |
rs545591469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296794 | CTGCACTCCAGCCTA[C/G]GCAACAGAGGGAGAC | 9474 |
rs545647942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207962 | TCAGGCATGGTGGCA[C/T]GTGCCTGTAATCCCA | 9474 |
rs545652100 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106236123 | TCTTTGTATTGGTTC[-/T]TTTTACTCAATGTAA | 9474 |
rs545727423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299673 | TACTCCATTTATGTG[C/T]GTGTGTATGTTTGTG | 9474 |
rs545848966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221994 | CCTTCCAGGTTCAAG[C/G]AATCCTTGTGCCTCA | 9474 |
rs545855091 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218655 | TTTATATGAAGCATC[C/G]GCAGCTAAAATGAAC | 9474 |
rs545867385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320790 | AGGGGGAATCTCAAT[A/C]TCATCCACCAGTCCT | 9474 |
rs545871305 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106260630 | TGCAATTCTCTGAAT[-/G]GCTAATTAAAATACC | 9474 |
rs545886649 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106298858 | CTATAAAAGAAAACA[A/G]AACTGGCAAAAATTA | 9474 |
rs545906747 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226269 | AACCTGAAAGAATTA[C/G]TTCAGGAAAGAAACT | 9474 |
rs545926624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269891 | GCTCAAGTGCCCCCA[A/G]AGTAGGAGCCCAGGC | 9474 |
rs545928200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262493 | ATTAGAAAAGTAAGT[A/G]CATCTAAAGTTTTCC | 9474 |
rs545949393 | snp | C/G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327198 | AAAAGTATATAAAAT[C/G/T]TCCTTTAAAATGTAT | 9474 |
rs545952640 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106293315 | AACCACTCCATTCCC[A/T]TAGAAACCTCAATAT | 9474 |
rs545956963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193486 | ACATAAACTAAAATT[A/T]AAATAATATAAAAAA | 9474 |
rs546002601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285494 | AGATGCTAAGTTTTG[C/T]TCTGGCTGGCAGTTA | 9474 |
rs546043107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284823 | ACAGAAATGTCTATT[C/T]GAATCCTTTGACTAA | 9474 |
rs546140774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106248674 | GGTGCAGTGGCCCAC[A/G]CCTGTAATCACAGCA | 9474 |
rs546169633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291996 | AGAATGAATGAGCAA[C/T]CTTTGGGCAGTAACT | 9474 |
rs546189509 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197838 | TTCTTTATAGCAACA[C/T]AAACAGACTAACACA | 9474 |
rs546211051 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251103 | CACTAATGGGCGCTT[A/G]CCCTTATCAACATCT | 9474 |
rs546231605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206520 | CTGGGCATAGTTGTG[C/G]GCGCCTGTAATCCCA | 9474 |
rs546246936 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305289 | TTACTATATGTACTA[C/T]TTCTTTAAAAAATCT | 9474 |
rs546271630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106312232 | CTGGAGTAAGTTACC[A/G]ACTATCTGGGATAAG | 9474 |
rs546276252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205943 | TTTCTGTTTAATATT[G/T]ATTATACAGTACCTT | 9474 |
rs546288467 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274157 | AGTCATGGTAAAAAC[A/G]TTTTTTATAGATTTC | 9474 |
rs546310693 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106312698 | AAAACCAAGGATACT[C/G]AGCACTGCAGGGCTA | 9474 |
rs546317338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106305122 | AGATGAATTTTATTC[C/T]ACATTAATTATATGC | 9474 |
rs546319182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312902 | TGGTAGGAGGTGGAA[A/G]GCAGAGAATGACTAT | 9474 |
rs546323498 | in-del | -/AC | 0.00636936 | 0.0560724 | intron-variant | ATG5 | GRCh38.p7 | 6:106248020 | GATTGCCACTGAAAG[-/AC]ACAGTTTGGAAAACC | 9474 |
rs546344309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220370 | AAAGTATAATATAAA[A/G]TCCCAAAAAACCTTG | 9474 |
rs546375459 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200833 | TGAAAATTTCCCCTA[C/T]AGTTTAGTAAGCATT | 9474 |
rs546381396 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184094 | ATAAGTCAGTGGATT[C/T]TTTTATCCTTACATA | 9474 |
rs546446594 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283046 | TCCTCCTGGTTCAGC[C/T]TCCCAAAGTACTGGG | 9474 |
rs546454507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106191919 | GATTCAATTATGTGA[C/T]TGGCATACAAAGGGC | 9474 |
rs546458198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234378 | CAATCCCTGTACCTG[A/G]ACAATGGAACAACTA | 9474 |
rs546495029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233896 | ATGAAGAATGCGGCT[C/T]CCCAGAAATATTGAT | 9474 |
rs546523227 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258689 | GAAGATTTTTAGTTA[C/G]ATTTCTATAAATAAA | 9474 |
rs546549384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254940 | CCATAATTGGGAGAA[C/T]AAAAGCCCTAACACA | 9474 |
rs546557754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297001 | GAGACAGCAGTACTC[G/T]AGACTTTAATGACAA | 9474 |
rs546558433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199913 | ACCTTACTATAAAGG[C/T]TAGTAAAGTTCAAGG | 9474 |
rs546575361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106248934 | CAAGAGCGAAACTCC[A/G]TCTCAAAAATAAAAA | 9474 |
rs546588510 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106189534 | GCTGAGGTGGGAGGA[C/T]TGCCTGAGCCCAGGA | 9474 |
rs546609927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298407 | TAAATTTAAATTAGC[A/T]GGGCGTGGTGGCATG | 9474 |
rs546613745 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187877 | CAAAATACTACAGTT[A/G]ATAAAAGAATGTGAA | 9474 |
rs546675340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197242 | GGTAGTCATTTGAGG[C/T]TGGGTGCAGTAGCTC | 9474 |
rs546680960 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192217 | TAGACTTTAGGTAAG[G/T]TTATTTTTTTTAAAA | 9474 |
rs546714094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106205025 | ATTTAAAATAGCCAT[C/T]CCTCACTCAGGGTTT | 9474 |
rs546719521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296392 | ATTTGTCAATTATTC[C/T]CAATAAGACACTAAA | 9474 |
rs546748329 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106261026 | ACTGATTGTTGAGTT[-/A]AAATGTGTATCTAGC | 9474 |
rs546773335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253860 | CATCTCCTTACTGCC[G/T]GCATCTGGGGCAGAC | 9474 |
rs546793608 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266005 | AAGATCAGAGCAGAA[C/T]TGAAGGAGATGGAGA | 9474 |
rs546811256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292654 | TTCAAAACTTTAAAT[G/T]TTATTTTTTATAGAG | 9474 |
rs546826065 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106198664 | CACCTGTAATCCCAG[A/C]TACTAGGGAGGCTGA | 9474 |
rs546828529 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242116 | GTGGAAATTATATCT[A/T]TCTATATCTATACAC | 9474 |
rs546837949 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297522 | CCTCTCAGAGGTATA[C/T]TTGAATGTATAAAAA | 9474 |
rs546847976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292233 | ACTAATATAAGAGAC[C/T]GACATGGTGGAATCA | 9474 |
rs546851819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190302 | TCTCATATGGAAGAA[C/T]GTGGAAGTGTGAGAG | 9474 |
rs546859658 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191466 | TATCTGGGTCTTTTA[C/T]GTCTAAACAGCAAAA | 9474 |
rs546861216 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276222 | GTAATCCCAGCACTT[A/T]GGGAGGCCGAGGCGG | 9474 |
rs546883791 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325635 | CCTGACACACTGTCC[G/T]GCGGGGACGCGGTAG | 9474 |
rs546900090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284194 | CAGTTCTCTTGGGAA[C/T]ATTACTAGGAATAGA | 9474 |
rs546924989 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325778 | GGAGCCCTGGCAGCG[C/T]ACCACAAGTCCAGTC | 9474 |
rs546975028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106238610 | GAACTAGCAGGCATA[C/T]GAACAGAAAAAGCTG | 9474 |
rs547064144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303615 | AAAAAACAGAAAACT[A/G]CAATCCCTCTTATGA | 9474 |
rs547066524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106246442 | CACACCCTTTCTCTC[C/T]CTCTCTCTCTGAAAC | 9474 |
rs547073228 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268286 | GAAAAAAAGCTCATC[G/T]TCACTGATCATTAGA | 9474 |
rs547085538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106300474 | TCTATCATGTCTATG[C/T]TTAAGATCAACATCA | 9474 |
rs547092534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193736 | ATAGGGTCCATTAAT[A/G]TTTGTCAAGTATGAA | 9474 |
rs547104923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253315 | GTGGGCTAGCCTCTG[C/T]GTCAGGGCTGAGCAG | 9474 |
rs547122780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293431 | TGTATTCATAAAGGA[C/T]AGTTGATTTTTGTAA | 9474 |
rs547174325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243056 | TTTAGAAGGTGCCAA[A/G]TTAATCCCTGACATC | 9474 |
rs547193045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275162 | TTAAAGCATCAGTAG[A/G]AGTTAAAGGGAAAAA | 9474 |
rs547208154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280479 | ACTATAAGTCAATTA[C/G]ACCTCAATAAAGCTG | 9474 |
rs547237209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315591 | ACATATAACATACAA[C/T]AGCTCAGTGAACGTA | 9474 |
rs547257162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233484 | AAGACTTTTCTTTAC[A/C]TGTCACAGAAAAAAA | 9474 |
rs547283815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106325263 | GCCTGCGACTAGACT[C/T]TCGCTTTCCTACCTT | 9474 |
rs547326028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106186904 | TCTGTTGCTGTATGT[A/G]AAAGTATTACTTCTT | 9474 |
rs547327824 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106273247 | AGAAATTAAAGACTC[-/A]AAAATAGATACACAG | 9474 |
rs547337829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239271 | AAAATCTACAAAACA[C/T]CTGGAAATAAAAAGA | 9474 |
rs547339356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293913 | ATTAAATAATACAGG[C/T]TGAGTATCCCATTTC | 9474 |
rs547345282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194294 | GCAGTGCCATCACAC[A/T]GACAAATGTGATTAT | 9474 |
rs547368370 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246397 | TCTCTCTCTCTCACA[-/CA]CACACACACACACAC | 9474 |
rs547382131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322823 | TTTGAACTGGCTGGC[G/T]TCACATATACCACCA | 9474 |
rs547419440 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224594 | TAAGACCAGAAATAC[A/G]GCCAGGTGCGGTGGC | 9474 |
rs547459181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269991 | TCTGTATTGCACTGC[A/G]AAATAACTGCCTAAA | 9474 |
rs547460922 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106314446 | CCTATAATCCTAGTT[A/G]CTTGGGAAGCTGAGG | 9474 |
rs547464359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234546 | TAACTCCTCCCACAC[A/G]AATAGTCTGCCTACC | 9474 |
rs547515611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228768 | TACTGGGCACCTGTC[A/G]GCCGGTTAAAAACGA | 9474 |
rs547551013 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226930 | AGAGAGGGAAGAAGG[A/C]AGGAAGGAAGGAAAG | 9474 |
rs547593806 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106265192 | AAAAAAAAAAAGCAG[A/G]GGTTGCAATCCTAGT | 9474 |
rs547594032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106264149 | TTTGAGAGGAACACA[A/C]ATGACCTGATGGAGC | 9474 |
rs547596109 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106256664 | CCTAGGCTATAAACC[G/T]ATATGGTATGTGCAA | 9474 |
rs547613823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323072 | TACAAGCGCTTGCCA[C/T]CAGGCTCGGGTTTGT | 9474 |
rs547622072 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259354 | CAATCAGGATTTCCA[G/T]GAATCCTAACAGTAA | 9474 |
rs547652519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230592 | TTAGGACCATAGAGG[A/G]CGCTCTAGGACTAAT | 9474 |
rs547731921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106263625 | GGCTGGCATCAGGCC[A/G]GTGCCCCTCTGGGAC | 9474 |
rs547737659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235740 | ATTCAAGCCGGCAAC[A/G]GCTACCTTCTTTGGG | 9474 |
rs547750393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292779 | CTGGCCCAAAAACTC[A/G]TAAATTTTAAAAAGT | 9474 |
rs547750438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299722 | CATGGTGTAGCAATA[A/G]TGGATATTCTCAGAA | 9474 |
rs547780586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222103 | CACCACGTTAAACCA[C/T]GAGTTTGGCCAGGAT | 9474 |
rs547806830 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300228 | GTAAACTGTTCAAGG[C/T]CACTGACAAGGTCTG | 9474 |
rs547807153 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311167 | ACATACTAGAATTCT[G/T]TTCCACTCCAATGTG | 9474 |
rs547823840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277192 | ATACCTACAAACACC[A/C]ATTTGATGTGGTAAT | 9474 |
rs547831698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192783 | CTGCCTAGAAGTTTT[A/G]AAAAATAGAGCGACG | 9474 |
rs547839431 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326587 | GTCTCAAAAAAAAAA[A/T]AGTAATAATTGGTAA | 9474 |
rs547869337 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322980 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCTC | 9474 |
rs547886890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198952 | AAACAAGGATTTGAA[C/T]AGACACTTCATCAAA | 9474 |
rs547907802 | snp | C/T | | | upstream-variant-2KB, intron-variant | ATG5 | GRCh38.p7 | 6:106325463 | CCTACCACACCTACC[C/T]GGCCCCTCCCCAGCC | 9474 |
rs547911828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299176 | CTGGATACCAAAATT[C/T]GCAGATGCTTAAACC | 9474 |
rs547912706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200188 | TTTTGGGCTCCATAT[G/T]CTTTGCTTAGTCATT | 9474 |
rs547999706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208140 | TCATTTATTATGGAA[C/T]CATGGACACAACTAC | 9474 |
rs548003446 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186139 | TTGAAAATTAAACCA[A/G]TGTTTCCACTTTCAT | 9474 |
rs548012752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256573 | ATTTCATCATGCGAA[C/T]ATCATAGAATGTACT | 9474 |
rs548015886 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279217 | GTATTTTCTAAACCA[C/T]AGCAAGGAGAAAGGG | 9474 |
rs548021814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106321891 | GTTAGCACATAGTAG[A/G]CTTTGAAATTTTTGT | 9474 |
rs548031958 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302392 | TTATACTGTAGATGA[C/T]GGTAAGTCAGAATAG | 9474 |
rs548036584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106207643 | AACATTAACGTTGAT[A/G]AAACAAGAAATGATG | 9474 |
rs548037868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222742 | ATCCTGGCTCTTCTA[A/T]TTACTAGGTAGGTAA | 9474 |
rs548040508 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238994 | TAATTAGAAACGCTA[A/G]AAGGAAATCACTTAG | 9474 |
rs548089838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306916 | AGAACTACACAAGAA[A/G]AATCAGAGGAGTCTG | 9474 |
rs548091101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314033 | GTGAAGAATTAGGAA[C/G]AATTCAAGAAAAAAC | 9474 |
rs548108263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278781 | GGAGGCAACACGACT[A/G]TGTGCTTTGCTATCT | 9474 |
rs548129364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106314643 | GGCCAAATATACTCT[C/T]ATACTCTCACATACT | 9474 |
rs548143356 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106224470 | AACTTGAAGAAAAGT[-/AAAG]AAAGAGGAAACTGGA | 9474 |
rs548145613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286652 | ATGTTACCCCAGTGA[C/T]TAAGTCATGTTATAC | 9474 |
rs548147398 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272145 | AATACATATCACCAC[C/T]GGTATAGACCACTGG | 9474 |
rs548163538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106285994 | TCTCTCCACTTTGAA[G/T]GAGCTGGAATCCAAC | 9474 |
rs548166855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249869 | TGACTATGCTGAGCA[G/T]CTTCTCATGTGCTCA | 9474 |
rs548181128 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311246 | GAGTCCTTCCCCTTA[C/T]ACAGCATACAGGTTA | 9474 |
rs548246393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233994 | ACTGCTATAACTCTG[C/T]CACTCTTTGCATGCA | 9474 |
rs548278184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206975 | ATGCAATCTAAATCT[C/T]AGGTTGACAGACAAG | 9474 |
rs548300114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106249443 | CTTCATTTGCTTTTA[C/T]GGCTGAATAATATTC | 9474 |
rs548302385 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298323 | ATGGTAAATGACGAC[A/G]ACTCCTTTGTCTTGG | 9474 |
rs548305698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240255 | AGATATCATAAAAAT[C/G]AAGATGAATTATACA | 9474 |
rs548343209 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248360 | TGAAAGGACATCACA[A/T]ATATTTTCTTATTTT | 9474 |
rs548351359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106279417 | GCTATACCCAAGTTT[A/G]TATGACATATGCCAT | 9474 |
rs548354833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292055 | CTCAGACACCTAAAT[G/T]ACTTTTTCAAACTCT | 9474 |
rs548391408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271317 | TAACCTCCAACATGA[C/T]AGATAAAGTGGTGGG | 9474 |
rs548448223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313934 | TGGTTTTAAATTCCA[A/G]TTTTTTGTTTTATGT | 9474 |
rs548518237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269361 | CCCAGCTGGCTTCAC[C/T]GGGGCTGCTGGTGGA | 9474 |
rs548519322 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278408 | TATTTGTATTTCAAT[A/G]TCATAAAATATCTGA | 9474 |
rs548622853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228315 | TCCATCCCTCTGGAT[C/G]TAGCAGGGTGTCCGT | 9474 |
rs548623310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284422 | GTTGCAGACATGCCA[C/T]CAGGAATCACTGCTC | 9474 |
rs548624002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191822 | AAAGTAAAGAGCGAT[C/T]GTAATTCTCTTCCTA | 9474 |
rs548650755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237479 | GTTCCATTGCTTACC[A/G]GCTGGCTGTCCTTTG | 9474 |
rs548660576 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208985 | CACAATGTGATATCA[C/T]TACACACCTACCAAA | 9474 |
rs548660852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191187 | TGAATCAATTTCTGG[C/G]GTAAAGTCTTTTTTT | 9474 |
rs548703479 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325928 | TACGCTTGAACTCGC[A/G]ACCAAACCTCTCCAA | 9474 |
rs548705514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106196642 | AGCACAAGATTGCTT[A/G]AACCTGGGAGGCAGG | 9474 |
rs548717287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306322 | CCACCATGAGGGACA[A/G]CATAAAACAGCAGCT | 9474 |
rs548735596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106255894 | TGTTACAATCATCTA[G/T]AGATTTATAACCAAT | 9474 |
rs548736381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260739 | AAAAGAGAAACAGTA[A/T]CCAATGAGTAACAAG | 9474 |
rs548783941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230817 | AAACCTGGCATCCTG[A/G]GGGAAGCATAAATTA | 9474 |
rs548844272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222035 | TAGCTGGGATTACAG[G/T]TGTGCGTCACCCTGC | 9474 |
rs548845925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213292 | AAAGCACTATGAAAA[A/C]AATTACAAAGCTTGA | 9474 |
rs548863362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302700 | AGTGAGCTCTTTTTT[C/T]ACTACAATAGAATCA | 9474 |
rs548879093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320003 | TCCAGAAACACTATA[C/T]ATTTTACATTACCTC | 9474 |
rs548879721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252687 | TCCCCCACGGGAGAC[A/G]TGGAGGACATATAAG | 9474 |
rs548881448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106313286 | TCATATCATTTCTCT[C/T]TTCTTCATGAAAGAG | 9474 |
rs548913000 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG5 | GRCh38.p7 | 6:106320894 | GAGTCAGAGAGGCTA[A/G]CCAGGTAGTAATTTC | 9474 |
rs548918504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106259949 | AAGGATGTGTTCATG[C/T]CCTTTGCAGGGACAT | 9474 |
rs548935436 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306569 | AAAGAATTATCAAAT[C/T]CAAAATGTCAGTAGT | 9474 |
rs548946762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273276 | AGGTAGTAGCTGCAT[C/G]AAGTCTAAAAACTCT | 9474 |
rs548973940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225849 | ACATCACATCTGCCA[A/T]GAGATAGCAATAACA | 9474 |
rs548987259 | in-del | -/CACCTAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288115 | AGCTGAGATTACAGG[-/CACCTAC]CACCATGCCCAGCTA | 9474 |
rs549006239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231207 | AGACCTAGGTAAATT[C/T]TCAGATAACCCTAAT | 9474 |
rs549023274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188578 | GATGCACAGTGTATC[C/T]GAAAGGCAAAAGACC | 9474 |
rs549027268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310262 | TTTTAAAAGAATACT[C/T]ATTTTTAAGGCAGAA | 9474 |
rs549046099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323474 | GAGACAGGGTCTCGT[A/T]ATGTCGCCCAGGCTG | 9474 |
rs549050296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223599 | CATTAACAATATTAA[C/T]GCTAAAGCAGATGAT | 9474 |
rs549050388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215070 | CTAATACAAAAAGAA[C/T]GTAATTAATAAACTA | 9474 |
rs549058326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288956 | TGTGTGTGTGGCAGA[A/G]GCAACAGGATCTCTT | 9474 |
rs549061258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308584 | TAAGGAAAAACAGCC[A/G]TGTTCTTTGCATTAT | 9474 |
rs549077752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258132 | CTCAAGTCCTTCCCA[A/C]CCACCCCCACTCCCC | 9474 |
rs549085504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223108 | CCCAGCTATAAATAA[C/G]TCAAATAATTTGCCA | 9474 |
rs549093416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314416 | CTAAAAATTAACCGA[A/G]CATGATGGCACATGC | 9474 |
rs549108934 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254527 | AGACAATAAAAACAA[C/G]GGAATAGCAAACAAA | 9474 |
rs549109567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323127 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 9474 |
rs549123917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244549 | GAATGCAACATTTCC[A/T]CAAGGTAGCCTTCTC | 9474 |
rs549226319 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290905 | ACAGTGGCATCATGT[C/T]TTCCAAAATTCAAAT | 9474 |
rs549262928 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106243862 | TAAGTAAATAAAATT[A/T]AAAAATATATAAAAA | 9474 |
rs549266530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217953 | AATGGAAGTTTTAAA[A/G]TAGTATAAACATTTT | 9474 |
rs549282960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317165 | AATAACACATCACAA[A/T]ACACGATATGAGTAA | 9474 |
rs549298295 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236551 | CTAGGGAACGTGAAG[C/T]AGTATCTCACTGTTA | 9474 |
rs549341327 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185942 | CAAAACATATTTAGA[G/T]GCTTTATTTAAAAAT | 9474 |
rs549355042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280580 | CTAAAGCAATGATCA[C/T]TGGACATATAGGGAG | 9474 |
rs549368812 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106198425 | TGAACACAATCCATT[A/T]AAAAAAACTTGATAG | 9474 |
rs549410184 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221396 | CTTTTATCAAATGTC[A/C]AAACTGAGGCCGGGT | 9474 |
rs549410291 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106265019 | ATGTAAATGGGATAA[A/T]TGCTCCAATTAAAAG | 9474 |
rs549435804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314980 | ATAAAGATGATTTCA[A/G]ACAAAATCCCAACAT | 9474 |
rs549443057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251125 | TCAACATCTCAATTT[C/G]CTTGCTCTGGAGGCC | 9474 |
rs549459233 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262624 | ACAAACACAGAAGGC[A/G]GCAGGTGATTTCTGC | 9474 |
rs549474761 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106230040 | TACCATACAAAGGTC[C/T]GACCAGACCTAGGAG | 9474 |
rs549478970 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106252856 | TACAGCATTTCAAAT[-/A]AATGTCGGATTGTGA | 9474 |
rs549530907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106186963 | ACGTTAATGAAACTG[C/T]AGTGGCAAAAACAGC | 9474 |
rs549547993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264338 | CTCCAAGAAATATGG[A/G]ACTATGTGAAAAGAC | 9474 |
rs549563603 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275295 | ACATTTACCAAGCTA[A/C]AGATTTCCGAAATGA | 9474 |
rs549579611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273106 | AAAAGGAAGCTTATC[C/T]AATATCAGTCTTTCA | 9474 |
rs549591012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202977 | CCCCAAAACTTAACC[A/C]TCTAATGGTTGAGAG | 9474 |
rs549598815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194911 | TGTGTTATTTTTAAT[A/G]TACAAAGAAAAAAAT | 9474 |
rs549616383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272588 | CTACAACTCCAGTTA[C/T]AAATGTAACAATTAC | 9474 |
rs549623665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209454 | ACACTGCATGACTCC[A/C]CTGATATAACATTAG | 9474 |
rs549632754 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227489 | TAGTCCCAGCTACTC[A/G]GGCGGCTAAGGTGGA | 9474 |
rs549639329 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106243807 | GTGCACTCCAGCCTG[G/T]GCGACAGAGCAAGAC | 9474 |
rs549683136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258889 | TAGTATTTAGAGATG[A/G]CAGAACAGCACAGCT | 9474 |
rs549690171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259089 | TCTCATCTTAGTTCA[A/G]CTTTTAGCTACTGGA | 9474 |
rs549731293 | in-del | -/TACCA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216217 | GTTTAAACGTGGAAT[-/TACCA]TGCAACCCAGCAATT | 9474 |
rs549732067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187747 | GGGCAAAATGAGCTG[A/C]TGATGTATGGTGATA | 9474 |
rs549757760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230277 | TGACTCAAAAGCTTA[C/T]TTATACCCTCTCTGA | 9474 |
rs549760179 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216989 | GTTATCATATGGGTG[G/T]CAGGGGAAATCATTC | 9474 |
rs549807525 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199462 | AAAAAACAGTTGCAC[A/C]AGACTATATGCTGTA | 9474 |
rs549810887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222904 | GGTATTCAATAAAGC[A/G]CAATAAATGTTAGCT | 9474 |
rs549882977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264219 | GTATCAATAGCCAAA[A/C]TGATCAAGTGGAAGA | 9474 |
rs549884741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228917 | CAATTTTCCTGGGGA[A/G]GCCAAGGGCTGACTA | 9474 |
rs549899729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316978 | AAACCATGCTCACAG[A/C]CCTCTGGCCCCAGTG | 9474 |
rs549924494 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106266294 | CTGCCAAGACTAAAC[C/G]AGAAGAAGTTGAATC | 9474 |
rs549936654 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202715 | CACCCCGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 9474 |
rs549966269 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106250260 | TAACTGTATATTTTT[A/T]AAAAATTTCTTCTTA | 9474 |
rs549968259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257969 | AGGAGCTGTAGAGAA[C/T]TAAAAAGCAAAAACC | 9474 |
rs549973287 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263879 | ATCCACAAAGATGGA[-/A]AAAAAAAAAAAAAAC | 9474 |
rs550034751 | in-del | -/TAGAGAGTACAGATTACTACACAA | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106256597 | TGTACTTAGAAAACC[-/TAGAGAGTACAGATTACTACACAA]TAGAGAGTACAGATT | 9474 |
rs550047134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224890 | CTTGTCTCAAAAAAC[A/G]AACAAACAAAACAAA | 9474 |
rs550108126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106294018 | TCATATTCTTACCAT[C/T]TGAGCATCACAAATC | 9474 |
rs550121938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230689 | CTCAAGGCAAAAACA[A/C]CCCTAAGATGTATTC | 9474 |
rs550177929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208223 | ATGTGTATATATACA[A/T]CTGTGTAAACACATA | 9474 |
rs550243770 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218829 | GAAAAAAACTTTAAA[A/C/T]GTAAGTTAATACAGG | 9474 |
rs550299922 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211433 | GAGATTGGACAGGCC[C/G]GGCGTGGTGGCTCAC | 9474 |
rs550329421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248016 | ACTTGATTGCCACTG[A/G]AAGACACAGTTTGGA | 9474 |
rs550333857 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230614 | AGGACTAATGCTCAT[C/T]GGAAAATGACTAGTG | 9474 |
rs550360846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300464 | TCTGAGTCATTCTAT[C/G]ATGTCTATGTTTAAG | 9474 |
rs550366388 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106247376 | CAGCACTTTTAAAGT[A/G]CAGAAACATGGAGTT | 9474 |
rs550372351 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257624 | CTCTTGGTAGTTCTG[G/T]GAACTCATTTCCTCA | 9474 |
rs550384192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208749 | TAAGCCGCAGGCTGG[A/G]AGAAAATATTTGCAA | 9474 |
rs550385640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318008 | GATGATGAAGAGAAA[A/C]ATAATTTGAGACGAA | 9474 |
rs550393469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106202238 | AGATGTGGTATCACT[A/G]TGAAAAATGTTTAAC | 9474 |
rs550421272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215842 | GAATGGGACAAAATA[C/T]TTGCAAACCATATCT | 9474 |
rs550430179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201334 | CTCTATCAGTTAATG[A/G]ATTATGGGCAGTTTT | 9474 |
rs550439458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315392 | TATTCAGTGAACAGG[A/C]AGGATGTCATCTCTG | 9474 |
rs550441490 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215084 | ATGTAATTAATAAAC[G/T]ATTTTCCTCTGAAGA | 9474 |
rs550478577 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195788 | AGGTTGTGTGGCTGC[A/G]CTGCCTCACTGCTCC | 9474 |
rs550524315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303576 | ATAAAGCCCGTATAA[A/C]CCTAATGCTAAATCA | 9474 |
rs550524444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295667 | CTCCTGGGCTCAAGC[A/G]ATCCTCCCACCTCAG | 9474 |
rs550558772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106195725 | TCTGTCACACAGATG[C/T]ACTCACCTACAGCAC | 9474 |
rs550562995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296287 | CACTTTTATAAATCT[A/C]AGATATATTTTAGGG | 9474 |
rs550575942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212387 | GGCTCATGCCTGTAA[C/T]TCCAGCACTTTGGGA | 9474 |
rs550593679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203692 | CAAGTTGCAATCCTC[C/T]ACCTAAGCCTCCAGA | 9474 |
rs550605013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267629 | ACAGCATGGTACTGG[C/T]ACCAAAACAGATATA | 9474 |
rs550620076 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192810 | GACGAGCTTTCTGAT[C/T]ACCACTAGCCTGAAC | 9474 |
rs550643116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262184 | TTCAAGTGATTCTCC[G/T]GCCTCAGCCTCCTGA | 9474 |
rs550656260 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209074 | TCCTTCACACACTGA[C/T]GGTACAAATGCAAAA | 9474 |
rs550664221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106195948 | TCACAAATTTGTGTG[C/T]CTTTCTTGTGTAGGG | 9474 |
rs550670194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318573 | CTAGTGAAAGATAAA[C/T]TGGTACTTTATTTCC | 9474 |
rs550701387 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235946 | TGGGCATTTCCATCA[C/T]GCCCTAAAAGTTCCT | 9474 |
rs550748717 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106293886 | GTAAATTAGCTTACT[C/T]GGTTAATCAGAATTA | 9474 |
rs550749545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291505 | CCTGATGAATCCATT[C/G]AAAGGGTTTCAGGAA | 9474 |
rs550781611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106189429 | GGGCAACAGACCCCA[C/T]CTCTACAAAAAATAA | 9474 |
rs550790816 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106198523 | AGCTCACACTTGTAA[C/T]GCCAGCACTTTGGGA | 9474 |
rs550800172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324374 | CTACACCATTTTATA[A/T]CAGGGACTTGAGCAT | 9474 |
rs550807893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209639 | ATATGTGATAAAGAT[G/T]GCATAGAACTAAATA | 9474 |
rs550824965 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241851 | GTCTGATGAGGTAGG[A/C]TGCAGACTCAAGGAA | 9474 |
rs550826755 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216178 | TGCAGATGCTTTGGA[A/G]AACAGTCTGACAATA | 9474 |
rs550863567 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219079 | TATTGAAATATATTA[G/T]TTCTTTCAAATTTTA | 9474 |
rs550887425 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191134 | GAAATTAAAAGAATA[C/T]ATACATATATATGAG | 9474 |
rs550893389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254112 | TAAATACCAAACTTG[C/T]TCCCATTTCAGTTTT | 9474 |
rs550930189 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267823 | CTATTCCTTACACCT[G/T]ATACAAAAATGAACT | 9474 |
rs550931441 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318443 | CCCAAAAGAGATACA[A/G]ATATAGACTTAGAAG | 9474 |
rs550957925 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285145 | CTGGGTAACTTCTAT[C/T]GATCTGTCTTTGAGT | 9474 |
rs550997183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252649 | GCAAAATAATTCTTA[C/T]GCCACAAATAACATG | 9474 |
rs551000331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225975 | TCCAGAAAGCCATAC[A/C]CATGTATAGAGCTGT | 9474 |
rs551003721 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263052 | AGTGGTCTCGCTCAG[C/T]GGGTCCCACTCCTAC | 9474 |
rs551012528 | in-del | -/AGAA | 0.00121286 | 0.0245959 | intron-variant | ATG5 | GRCh38.p7 | 6:106199814 | TTTCATGGTAATGAT[-/AGAA]AGAATTCAGTAACTG | 9474 |
rs551026324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210087 | TTCAACCTACTCTAA[A/C]ACACTTGAAGGCCAT | 9474 |
rs551039108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232011 | CCGCCCCCTCGTCCA[C/T]GCACCTCGTGTCAAG | 9474 |
rs551074119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106231327 | AAATGACAGAAGTGT[C/T]GCCGTAACTGCAGCC | 9474 |
rs551095644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259880 | TCTATCAATGATAGA[C/T]TGGATTAAGACAATG | 9474 |
rs551145051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273497 | GATTATTGCTTTACA[A/G]TCCTTGAATTTGAGT | 9474 |
rs551161506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323551 | GCCAAGTTATATTCT[C/T]TAGTTGCTCAGTCCG | 9474 |
rs551161895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253415 | CAGGGAAATCTGTGG[A/T]TTCAGTGAATCACAA | 9474 |
rs551180178 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262882 | CATGTAGCCTACACC[A/T]CCAGGGCCCTGGGTT | 9474 |
rs551181474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274423 | TTTCTCTTTCACAGA[A/G]TTCTGAGAAATTAAA | 9474 |
rs551260204 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188381 | AGCACTGAGTCAAAA[A/C]ATGAAAGAATAGTGG | 9474 |
rs551273472 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322888 | CAAAACGGAAAACCA[C/T]TTCAGATCTTCCTTC | 9474 |
rs551301355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260935 | GGCTTGACATTCTCA[A/G]TACAAATGATTTCTA | 9474 |
rs551319869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309983 | GCTCCTGATTTTGGA[A/G]AGTGTTGTATTACAT | 9474 |
rs551342019 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206348 | TGAAGCCTTGATCTC[G/T]GACTTCCCAGCCTCC | 9474 |
rs551342332 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262911 | TTTCAAGCACAAAAC[C/T]GGGCAGCCATTTGGG | 9474 |
rs551349667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219502 | AGGCTTTTTTTCTTG[C/T]TATCATTCCCTAACT | 9474 |
rs551365148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301558 | ATTTAGATTCATTCA[C/T]TCATTCATTCACTGA | 9474 |
rs551372159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106318387 | CCTTCCACATGTCAC[A/G]AACAGTAAAATGAAT | 9474 |
rs551374594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274202 | TTATAAGAAAAACAA[C/T]TTGATATTAAATAGG | 9474 |
rs551387186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209484 | GTGAAATGACAAAAA[C/T]TTTAGAAATGGAAAA | 9474 |
rs551427397 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106267590 | CCTGACTTCAAACTA[C/T]ATTACAAGGCCACAG | 9474 |
rs551447459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301635 | AAGAAAAATGATCCA[A/G]AATCTGAACCTTTTT | 9474 |
rs551449182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282528 | GTTAAGAACACATAC[A/G]ATGCATTATGGAAGT | 9474 |
rs551451592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251871 | AAAGAGACAGAGTCT[C/T]GCTCTGTCACCCCAG | 9474 |
rs551451909 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106252001 | ATGCATCATCACGCC[C/T]GGCTAATTTTTGTAT | 9474 |
rs551455155 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258108 | TTTTGCACTTGTAAT[A/G]CTTGATGGCTCAAGT | 9474 |
rs551460669 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260216 | TACTTATGTAACAAA[A/C]CTGCACGTTGTGCAC | 9474 |
rs551483825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309412 | AGAACGTGACATTGA[C/T]CCTAGGGGCTACAGA | 9474 |
rs551499363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106231518 | CTTGCGTGCTAGAAG[A/G]ACTAAGGAAAACTAG | 9474 |
rs551504190 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291164 | AAGACAACCATATTT[G/T]GCATGCAACAGAGGA | 9474 |
rs551541676 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318226 | GATTCCAGGACACCA[C/T]TTGACATGTTTATTA | 9474 |
rs551585627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216104 | AGAAAATAAGCGTTG[A/G]CAAGGATGTGGACAA | 9474 |
rs551609232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106203654 | ACTCTGTCACCCAGG[C/T]TGAATTGCAGTGGTG | 9474 |
rs551616617 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264576 | GAAGGAAAAAATGTT[A/C]AGGGCAGCCAGAGAG | 9474 |
rs551617687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210930 | TACTGAATTCTAATA[G/T]GTATTCTGTATTGAG | 9474 |
rs551656412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218724 | ACGTCAGAATTGTCC[C/T]AAGCTGATTCTAAGT | 9474 |
rs551666597 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215684 | TAAGAGGAAACCTTC[A/G]TGACCTTGGATTAGG | 9474 |
rs551687091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106311404 | ACGAAGTGTATCTTA[A/C]GGCAAAGAGTCAAAA | 9474 |
rs551724546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312111 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 9474 |
rs551742540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195027 | ACCTTTGGTCATTTC[C/T]TGTTACCTCCAACTT | 9474 |
rs551783525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106294867 | AAAAAAAAAAGAATT[C/T]AGGATGAACGCCCGG | 9474 |
rs551802223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258994 | ACATGAAGAAAGGCA[C/T]TGTGATAATCAATTG | 9474 |
rs551815723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216878 | CTGGGCAACACAGAC[C/G]ATGTCTCTAAATAAA | 9474 |
rs551841649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313121 | TACCACCAGCTTCCT[A/G]AGAAGGCAGAAGATA | 9474 |
rs551854976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224366 | CAGTGCAAATGGCAA[A/G]AAGGGAATAAATGAA | 9474 |
rs551881539 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228056 | GATTATTTTACAGCT[G/T]GGGTGCAATTATCCC | 9474 |
rs551891833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265594 | TTCTAAAATCGACCA[C/G]ATAATTGAAAGTAAA | 9474 |
rs551989101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221342 | CAGCTCTATTTTCAA[C/T]AGTTATAACATTTTA | 9474 |
rs551995116 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106290012 | ACACCAAATTTAACA[A/C]GTTCAGTTTATTATA | 9474 |
rs552006781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106200170 | CAGGCTGAATGACAC[A/G]TATTTTGGGCTCCAT | 9474 |
rs552018344 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237074 | GTTCCACTCCACATC[C/T]ACTGTACCTGAAATA | 9474 |
rs552024064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106262842 | TTCCCATGGTTTCTG[C/T]AATCTGCAGATCAGG | 9474 |
rs552047142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302543 | AACAATCCATGTGAG[A/T]AATCAGATGGGCCTG | 9474 |
rs552050923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245371 | TCAGGGCAGACTTCA[C/T]TTTTCATGATAATTA | 9474 |
rs552066962 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185098 | ATTCTTTTTGATTAA[A/G]CTTTACAATTTCCAT | 9474 |
rs552086287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295613 | CTGTAACCTAGGCTG[A/G]AGTGCAGTGGTGCAG | 9474 |
rs552105803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192874 | TGATATGTTCATTAG[C/T]AAAACACCAACTAAT | 9474 |
rs552166769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249049 | GGCACTTATGAAGTG[C/T]CAACTGCAGCTTAAT | 9474 |
rs552177416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242011 | CAGCATTATTCACAA[C/T]AGCCAAAAGGTGGAA | 9474 |
rs552181752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283736 | GGTATTTTATAGACT[A/T]CACCAATGAAACGAT | 9474 |
rs552187622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299120 | TGAACCTGGAATACG[C/G]TCCACCCTTGGTACG | 9474 |
rs552218366 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106305450 | TTTTTTTTCTTGTCA[C/T]TGAGAACTGTCACCT | 9474 |
rs552258347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212491 | CAAAAATACAAAAAT[C/T]AGCCGGGCGCTGTGG | 9474 |
rs552267446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191075 | TGAAGATGCCTATAT[A/G]GATGTATGGTTTGAA | 9474 |
rs552282706 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320507 | TAATGAAAGAGCTGA[C/T]ACCATAACCTGTCTT | 9474 |
rs552316486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291482 | TTATATCATGGAAAC[A/G]GATTTGACCTGATGA | 9474 |
rs552371830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276786 | CTCATCTTTTTCTAT[A/T]TAGGCTATCTTCTTA | 9474 |
rs552377887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247804 | AAGAAGGTAGAGCCT[C/T]GCTTTGATCAACCTC | 9474 |
rs552390768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106286538 | CCTCCATGATTTCCA[C/T]CACCTGGTATTCCTA | 9474 |
rs552391029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278251 | CCCAGCCAAAAATGT[G/T]TTATTTCTTTGTAAA | 9474 |
rs552403686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192070 | TTATGCAAATTAAAT[A/G]ACATTAAGAAAAATT | 9474 |
rs552424804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297888 | CTAGCCTGAGCAACA[C/T]GGCAAAACCCTGTCT | 9474 |
rs552426417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285793 | TCATGCAATTTTCAC[A/G]TCACAAAATATTTTT | 9474 |
rs552435945 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106283270 | TTCTTTTAATGTCTT[C/T]ATCAGGTTTCAGTAT | 9474 |
rs552476395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269287 | AGAGTGCTGATTGGT[A/G]TATTTACAACCCCTG | 9474 |
rs552505583 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ATG5 | GRCh38.p7 | 6:106207485 | GTGGGAGGAGAGCTT[A/G]AGCCCATGAGTTTGA | 9474 |
rs552512839 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303689 | TGAATCCAACAATGT[A/G]TAAAACTTATTACAT | 9474 |
rs552525804 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106239187 | AAGTTTGTAAAAACA[A/C]AATAGGATGAGATTT | 9474 |
rs552534528 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223742 | AGAGAAACTACATAC[A/G]TGGTGAAATATTTAA | 9474 |
rs552546728 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269196 | GCTAGTTACAGAGTG[G/T]CGATTGGTGCATTCA | 9474 |
rs552565455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233010 | CCCAAGACTTGAGCC[A/G]GTTCTCATACCTGGG | 9474 |
rs552604656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290864 | ATCTCATCAGAAAAT[C/T]ATTTAAGAATAAAGC | 9474 |
rs552604848 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326456 | GTGGCGGGCTTCTGT[A/G]GTCCCAGCTACTGGA | 9474 |
rs552618195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106211776 | CCAGTGAGGCTTAGA[C/T]GGACATTCTAGTCTT | 9474 |
rs552621520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198366 | TTGATTTTTAAAATA[C/T]GTAAATGTATTGCCT | 9474 |
rs552638447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297204 | TTTTATGACAAAAAC[C/G]TGGACCATTTCTTTT | 9474 |
rs552656935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211354 | ATGGAGGTGCTGGGG[A/G]AGTCTCCTACGGACA | 9474 |
rs552664992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106247029 | TAAATATTCTTCATT[C/T]TTCCAGTATATTGAG | 9474 |
rs552718242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262359 | ATGAGCCACTGCACC[C/T]GGCCGGTCTAGGGTA | 9474 |
rs552719263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205335 | AGTCAAAGGAATCTT[C/T]TCAAGAATTTGGAGC | 9474 |
rs552740640 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106268244 | AGGCACTTCTCAAAA[G/T]AAGACATTTATGTGG | 9474 |
rs552751118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106268558 | TATAAATCATTCTAC[C/T]ATAAAGACACATGCA | 9474 |
rs552785725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220468 | ATGATATCCTGATAT[A/G]AAATGTCAAACAAAA | 9474 |
rs552814519 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325890 | AGGCCCGAGTCGCTC[A/T]TGAGCATGCGCCAAC | 9474 |
rs552826783 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250335 | CTCTAATCTTCAACT[C/T]CAATGTGAAGGAAGA | 9474 |
rs552836717 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106233149 | TACAAGGTTTCCAAA[A/C]CAAAGGCTCAGCTCT | 9474 |
rs552842236 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106228219 | TGCACTCTTCTGGTC[C/T]GTGTTTGTTACGGCT | 9474 |
rs552844555 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232521 | AAGGACAATATGGAC[A/G]AGCAAAGAATGCCCG | 9474 |
rs552891160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227507 | CGGCTAAGGTGGAAA[C/G]ATCGCTTGAGCCCAG | 9474 |
rs552911165 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237713 | TGAAAATCCAGTCCC[A/G]AATTCCATAAAATGT | 9474 |
rs552925263 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325966 | GCTTCTACCCTCTTC[C/T]GAGAATCTTGCGTCA | 9474 |
rs552937044 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188935 | CTGACTTGCCTCAAT[A/G]ACACAATTTTAAACA | 9474 |
rs552944859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246726 | GTTTCCGGACTCTTT[A/G]TGAAATGTCTTCAGA | 9474 |
rs552963580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188940 | TTGCCTCAATAACAC[A/T]ATTTTAAACAGAGGG | 9474 |
rs552982013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323841 | AAATTAAGGTTCTTA[C/T]AAATTCCCACATGCT | 9474 |
rs553000413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188392 | AAAAAATGAAAGAAT[A/C]GTGGTGTAAGAGTAA | 9474 |
rs553006835 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213598 | AGACTGAATATAATG[C/G]TACTTCTGAGAAATC | 9474 |
rs553009603 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318601 | TCCCATATACCATTG[C/T]TGCTTACATGTATAT | 9474 |
rs553043643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295747 | TATTTTATTTTTTAT[A/T]GAGATAGTGTCCAAC | 9474 |
rs553079901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253512 | AGAAGACATTTACTC[C/G]TTTACCCTACAAAGT | 9474 |
rs553100488 | snp | A/G | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186614 | GTTCACTCAGCCACT[A/G]CAGAGGTGTTTCCAA | 9474 |
rs553126091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296735 | AGACAGGTGAATTAC[C/T]TGAACCTGGGAGGTG | 9474 |
rs553126902 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325646 | GTCCTGCGGGGACGC[G/T]GTAGCAGGACTCCAG | 9474 |
rs553145209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191309 | GGTAAAGATATGGCA[A/G]CTTTTGCTAATGTGG | 9474 |
rs553160486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281348 | CTTTGCAGTCAGTTC[C/T]CTCATTCCCTTCCCA | 9474 |
rs553161405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106275925 | ACCGAAAGTAGCCAA[C/T]GACAATACATAAGTG | 9474 |
rs553192766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106219040 | AAAGAGAAAAGGAGG[A/G]AAGAACACAAGGACA | 9474 |
rs553198462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284020 | CACTCCTTTTCATGA[C/T]CAAATTATACTCCAT | 9474 |
rs553226826 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262094 | TTCAGCTGATCTAGG[A/G]CAGAGTCTCGCTCTG | 9474 |
rs553244494 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106295118 | GACAAGTTATAGATT[C/T]AATCCAATTCTGATC | 9474 |
rs553299975 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292019 | CAGTAACTATGAATG[A/C/G]ACACCCCGATGGGAA | 9474 |
rs553308235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106291150 | AAGTGCTTTTCCTCA[A/G]GACAACCATATTTGG | 9474 |
rs553323111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273732 | AAACAATAATTTCTC[A/G]GTCTACTTATTCTAC | 9474 |
rs553366651 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185693 | AGGCTTACAGTGATA[A/C]AACAACAAAGATGAA | 9474 |
rs553369571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226084 | TAAAATCCAGTTATA[A/T]ATTGCTTGCCGTATC | 9474 |
rs553383999 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106321560 | AGACGGGATTTCACC[A/G]TGTTAGCCAGGATGG | 9474 |
rs553398130 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106310643 | ATACATTCACTATCC[A/T]TCTCCAGAACTTTTT | 9474 |
rs553432880 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310687 | GGAAACTGTACGTAT[G/T]AAACAGTAGCTCCCC | 9474 |
rs553446013 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ATG5 | GRCh38.p7 | 6:106269756 | GGCCCGCAAGCGCCG[C/T]GCACATCCCCGGTTC | 9474 |
rs553446426 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106292908 | ACTAATCGAAGCTTA[G/T]CAACTAAAACAGTGT | 9474 |
rs553450122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211885 | TATTCATCAGCTACT[C/T]TGTGTGTGTGCTTTG | 9474 |
rs553454483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285385 | TTGATATGGACCATA[C/T]TTTCTTGCTTATTTG | 9474 |
rs553481700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270783 | TCCCATCTCATTATC[C/T]AATATTTCATATCTC | 9474 |
rs553484019 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327420 | TAACAAAATGTTGGG[A/G]CCAGGCACAGTGGCT | 9474 |
rs553490720 | in-del | -/A | 0.249886 | 0.25 | intron-variant | ATG5 | GRCh38.p7 | 6:106263878 | AATCCACAAAGATGG[-/A]AAAAAAAAAAAAAAA | 9474 |
rs553500784 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323179 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 9474 |
rs553501674 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106237877 | AGGAGCATAAAGACA[C/T]AAGCACAGTACAGAG | 9474 |
rs553538904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237169 | AATTTTAAAATATAA[C/T]TTGAAAGTTAACAAT | 9474 |
rs553540461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245585 | GGTTTTGAGGCTTCA[A/G]CAAGATAAGATGGGC | 9474 |
rs553576418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311706 | AAGCCACAAAGGTTT[C/T]AAGCAAGCAAGTGAC | 9474 |
rs553597419 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106308049 | AATAAAATTGAATAA[C/T]GTCAAGAGATGACTT | 9474 |
rs553618841 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242853 | TTGCAAGATATCTAC[C/T]AAAATGGAAAACAAC | 9474 |
rs553625423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267407 | TCATGAAAATGGCCA[C/T]ACTGCCCAAAGTAAT | 9474 |
rs553625562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260254 | CTAGAACTTAAAGTA[C/T]AATTTTTTAAAAAAG | 9474 |
rs553643440 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ATG5 | GRCh38.p7 | 6:106225441 | CAATATACTGAGTTG[A/T]AATTTTTATATTTTA | 9474 |
rs553645334 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106269046 | GAACTTAAAGTAAAA[C/T]AAAATAAAAGTTTTC | 9474 |
rs553656280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266844 | CTAGGTATTGATGGA[A/C]CATATCTCAAAATAG | 9474 |
rs553719251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278828 | ACAGACATAGAGAGG[A/C]CAATCACTGACAGAC | 9474 |
rs553728582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262993 | AACCCCAGAGAGACA[A/G]AACCATTCATTCCCC | 9474 |
rs553751786 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245690 | AAAATAAATATTTCA[G/T]TAAAAATTATGCCCT | 9474 |
rs553763726 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106262482 | AACAAAAAAGGATTA[C/G]AAAAGTAAGTACATC | 9474 |
rs553782380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193007 | TCAAAGAGGGTTAAA[C/T]CAAGCCAGGATATAG | 9474 |
rs553788682 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326874 | GGGTATCTAAATCAA[G/T]TTAGGGAAGCATGCC | 9474 |
rs553797558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222411 | AATTTCCTAATTGAT[C/G]ATTAGGAAAATAACT | 9474 |
rs553798528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277496 | ATTTTGTCAAAACAT[G/T]AAAAACTCTTACCGT | 9474 |
rs553892800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234905 | TAGCATCAGTAGTCC[C/T]TCAAAATTGAAGAGC | 9474 |
rs553930240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268966 | ACGGGTTGATAGGTG[C/G]AGCAAACCACCATGG | 9474 |
rs553958000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303550 | GAACAGAACACTTTC[A/G]AACTCAGTTTATAAA | 9474 |
rs553982340 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215772 | CAAACTGGACTTCAT[C/T]AAAGTTAAAAACTTT | 9474 |
rs553986215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292416 | GACAAAATTAGGTCA[C/G]ACTAAATTCAGTCTG | 9474 |
rs553992262 | in-del | -/TGT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222375 | AAGTTTGAGACTTCA[-/TGT]TTTAATGTGATCACT | 9474 |
rs554004645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322033 | TATTTTAGAAAGATT[C/T]TCCCTCTCCTACATA | 9474 |
rs554018864 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292376 | GGCTAAGGGAATGAG[A/G]GACCAGCACTTCATA | 9474 |
rs554026262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106264473 | AGGCCAACATTCAAA[C/T]TCAGGAAATACAGAG | 9474 |
rs554083901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256092 | TAAAAACAAAAATAT[A/T]TTAATTTTTGAAAGA | 9474 |
rs554101705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106199878 | AGAGATACATGGATG[G/T]GTGTAAGACATCATC | 9474 |
rs554113351 | in-del | -/AAACA | 0.00239904 | 0.0345509 | intron-variant | ATG5 | GRCh38.p7 | 6:106212645 | GAGACTCCGTATATT[-/AAACA]AAACAAAACAAAACA | 9474 |
rs554124273 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250712 | ATGAAATCTCAAGCA[A/C]CTAGCATGGTGCATG | 9474 |
rs554126259 | in-del | -/A | 0.00256465 | 0.0357176 | intron-variant | ATG5 | GRCh38.p7 | 6:106274343 | AAATGAAAACTCATA[-/A]AAAAAAACACTGAAA | 9474 |
rs554142972 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184440 | TTAATGATTTTATCA[A/G]CAGGTAACTTGTTTT | 9474 |
rs554155099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306447 | ATTCAGGGACATCTG[A/G]CAACATTTTTGATAA | 9474 |
rs554176528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221461 | GAGGCCAAGATGGGC[A/G]GATCACTTGAGCCCA | 9474 |
rs554201283 | in-del | -/A | 0.266546 | 0.249452 | intron-variant | ATG5 | GRCh38.p7 | 6:106271789 | TACACAGAATGCTTT[-/A]AAAAAAAAAAATGGT | 9474 |
rs554214686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292368 | AGCAAGGTGGCTAAG[A/G]GAATGAGGGACCAGC | 9474 |
rs554222597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106234179 | ACCTCCCAACTGACC[C/T]GGGTACATAGCACCC | 9474 |
rs554246502 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106212865 | GCAAAAACAAAAAAA[A/C]CCCAAGCATACTATG | 9474 |
rs554251547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291880 | ACGTGTTTAATAACA[C/T]GGTATTGTGCAAAGC | 9474 |
rs554263041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277457 | TAATGGGGACAATTA[C/T]GATTGTTCCACAATC | 9474 |
rs554282984 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106319622 | CAGCTCAAAATAACC[C/T]TTCTTCTACACATGA | 9474 |
rs554302219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106285308 | TTAATTCATTTTTCC[A/G]GTAGTACCAAGATGT | 9474 |
rs554326824 | in-del | -/AATAAT | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106270427 | AACGTACTACAGGCA[-/AATAAT]AATAATAACAAAAAT | 9474 |
rs554331969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106200327 | TCATGCAAGTAATCC[C/T]GCATTCCTCCAATTC | 9474 |
rs554338278 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304861 | CTTTGGGAGGCCCAG[A/G]CAGGTGGAGCACCTA | 9474 |
rs554367331 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296015 | ACACAGAAGCTTGAA[A/C]AAAGTACATAATAAA | 9474 |
rs554384586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222265 | CTGCATCATTCACAA[C/T]CTATCTTTCAAAATG | 9474 |
rs554416922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320443 | TGGGCAGGTGCAATA[C/T]ATATGCCAACTTTTA | 9474 |
rs554431708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298277 | GCCTGTCAAAATCTT[A/T]AAATTTTTTTTTAAA | 9474 |
rs554453674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321509 | GACTACAGGCGCCCG[C/T]CACCGCGCCAAGCTA | 9474 |
rs554487219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106248482 | ATTTTTTTCTCATAA[A/G]AAAAACTGTAAACAT | 9474 |
rs554500310 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188629 | GCTGGAGTTTATGAG[A/T]TGTACAACAGAAGCT | 9474 |
rs554500703 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106323228 | ATCATTATCACTCTG[C/T]GGTCTTTTCCGTTTC | 9474 |
rs554511918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206451 | GTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAATAT | 9474 |
rs554514547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314360 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATA | 9474 |
rs554529446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268814 | TCTCACTCATTAGTG[G/T]GAGCTGAACAACAAG | 9474 |
rs554547047 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253152 | GGAGAAAAATAAAAA[G/T]GAACAAGTAGTAATT | 9474 |
rs554568384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106268095 | ATCAGAGTGAAGAGG[C/T]AACCTACAGAATGGG | 9474 |
rs554573104 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269636 | GTACACCCTCCGCAG[C/G]CGCTGGCCCGGGTGC | 9474 |
rs554648339 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106213532 | AGCTTGAAATACATA[-/T]TTTTTTTTTAAATAG | 9474 |
rs554700422 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241406 | GGTGGGAATGTAAAG[A/T]GGTACAGCTACTACG | 9474 |
rs554704642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265589 | GTGTATTCTAAAATC[A/G]ACCACATAATTGAAA | 9474 |
rs554726422 | in-del | -/TCTTCCCAC | 0.19459 | 0.243782 | intron-variant | ATG5 | GRCh38.p7 | 6:106196807 | AACACCCAACTAATT[-/TCTTCCCAC]TCTAGGCACTCCTTA | 9474 |
rs554737234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249140 | TTGAGATATAATTTG[C/G]ATACCATAAAATTCA | 9474 |
rs554739288 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106240736 | TCCATACCTTAAAAA[A/G]AATACATATGCTTAC | 9474 |
rs554741642 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106289156 | ACTCAATACATCCAA[C/T]CTGTTGAATGTATAA | 9474 |
rs554788779 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222040 | GGGATTACAGGTGTG[A/C/T]GTCACCCTGCCCAGC | 9474 |
rs554806023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278404 | TTATTATTTGTATTT[C/T]AATGTCATAAAATAT | 9474 |
rs554823279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270513 | GGCTCCATATTTCAT[C/T]GCTTTGTATGACTGT | 9474 |
rs554828527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229023 | ACAGTCGCCCATGCG[C/T]GCGCTCCTACCTTCC | 9474 |
rs554837256 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323364 | ACCTTGAGCTCAAGG[A/G]GGTCAAGTGATCCTC | 9474 |
rs554961138 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106220030 | TTGATAGCCTTTTTT[A/T]AAAAAGCTAACCATT | 9474 |
rs554961810 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273219 | ACAGAACCTGACACT[A/G]TAACAAAAAACACAG | 9474 |
rs554961848 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106228951 | GCAGAAAGCTGTCGT[-/C]CCGAACTCCCGGCAT | 9474 |
rs554962978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265372 | TTCTTCAAGATCTAC[A/G]AAGAGACTTGAACTC | 9474 |
rs554967566 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326371 | ACGAGGTCAGGAGAT[C/T]GAGACCATCATGGCT | 9474 |
rs554980468 | in-del | -/TTTAGT | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106274678 | AAACAAGACACTTCC[-/TTTAGT]TTAATAGGAAACTAC | 9474 |
rs555002805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106272105 | TTGCTTTTTCTCTCA[C/T]GGCACTCATCATCAT | 9474 |
rs555012097 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300836 | TATGTATTTTTTTTT[-/A]ACAATTCAAAAAGTA | 9474 |
rs555017564 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106286150 | GGAGAACATACACGT[-/A]ACACTTTGGCTCCTC | 9474 |
rs555053682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258494 | TTATCAATAACTTAT[A/G]CACTTGTAAAGAATT | 9474 |
rs555079404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323839 | ACAAATTAAGGTTCT[C/T]ATAAATTCCCACATG | 9474 |
rs555087878 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197177 | GGAAGTTTAAAACAA[C/T]ATATTTTAAAAAGTA | 9474 |
rs555090307 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106227688 | AAGACTGTAGATCAA[A/T]ACCATAGAAAATAAT | 9474 |
rs555095794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226861 | GGCTCAACAGCTGAT[C/T]TGGGCAGCCAGAAGA | 9474 |
rs555100300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295101 | ACATATATAGTACTA[C/T]AGACAAGTTATAGAT | 9474 |
rs555103999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318876 | ACACTTAACTTTAAA[A/G]ATATGTAAGAAAAAT | 9474 |
rs555114375 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307779 | GGCCCCAGGTGATCC[A/G]CCAGCCTCGGCCTCC | 9474 |
rs555118166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226257 | ATAAAAAATAAAAAC[C/T]TGAAAGAATTAGTTC | 9474 |
rs555129350 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252762 | ACCCTCATGCAGGAA[A/G]CCGATGAAATGGTCT | 9474 |
rs555188592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223472 | TCTCAATCTCAGCGT[A/C]GTAGATAGCTTAGGG | 9474 |
rs555264906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212013 | TTGTTATATTTGCAG[A/G]TGCTTAAAAAATCAG | 9474 |
rs555283952 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106212607 | CCGTCCCACTGCACT[C/G]CAGCCTGGGCGAGAG | 9474 |
rs555284291 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280274 | TGAAAGTATTATGTC[-/A]AAAAAAAAAAAAAAA | 9474 |
rs555299985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303985 | TAAGGAAAAAAAAAA[A/G]AAGAAGAAAAGAAAT | 9474 |
rs555315216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242342 | GACATCATGATATGC[A/G]AAATAAGCCTGTCAC | 9474 |
rs555322731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220581 | TGATAACCCTATATA[C/T]TACCTACTTAAAATT | 9474 |
rs555419927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223998 | CAAAAGGTAGAAGGA[A/C]ATGTTTCAAAAACAG | 9474 |
rs555444303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106214409 | ATAAGCACTTTCTGT[A/G]CTTATGTTGAGAGTC | 9474 |
rs555447306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316485 | TCAGATCAAAATTAC[A/T]TATGCCAGTAATATT | 9474 |
rs555475591 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285532 | GGCAGCTCTCCTTAA[A/T]CCTAAAAAGGCAGGT | 9474 |
rs555488564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249641 | GGTCATTAGGTAACT[C/T]TATTTAACTGATACA | 9474 |
rs555505038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200701 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9474 |
rs555528061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195233 | TTTCATCACTGAATC[A/G]CTTGTAGGGAGTAGA | 9474 |
rs555536974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271529 | TCTAGCCGCTAGATT[A/G]TGAAAATAATCAGAC | 9474 |
rs555550311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252129 | ACAGGCATGAGCCAC[C/T]GTGCAGAGCCAAACA | 9474 |
rs555562289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307035 | CAAAGGATTAGAGAC[A/G]GGACCCAAAATACAA | 9474 |
rs555573470 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298861 | TAAAAGAAAACAGAA[C/G]TGGCAAAAATTAAAG | 9474 |
rs555629676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256916 | CTTACTATAGCTTTT[C/T]CACTTTATAAACATT | 9474 |
rs555652822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301914 | ACTGAGATACAAAAA[A/G]GTCAAATAACTTGCC | 9474 |
rs555674181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106243297 | GATTATGAAAGTAAA[C/T]AAAACGAAGTTCAAA | 9474 |
rs555681930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259179 | GTTGGCTGAAAATTA[C/T]ATATATTTCTCAAAA | 9474 |
rs555702395 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106250341 | TCTTCAACTCCAATG[G/T]GAAGGAAGACTCGCA | 9474 |
rs555703646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217079 | TGTTTTATGCATTTT[C/G]TGGGTTTTTTAAAAA | 9474 |
rs555703971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209244 | ATAGCTGTTTTATTC[A/G]TGAGAGTCAAAAACA | 9474 |
rs555715156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106279027 | ACTAAACCATGATAA[A/C]TGAAATTCATGCATA | 9474 |
rs555739056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257518 | ACCACTATCATACAT[A/G]CAGTCCACTGTTGAC | 9474 |
rs555753029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299938 | TTGTAACTGCAAGCA[C/T]GTAACTACAAATGCA | 9474 |
rs555753781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287048 | TAATTTGTCAGACAA[C/T]AGTAGATAACTAATA | 9474 |
rs555779659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106208333 | TAAAATGCACAACAC[A/T]ATTCTGACACATAAC | 9474 |
rs555787471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106193231 | ACCCATTTAAAAATA[C/T]TTACATTAACTTCTT | 9474 |
rs555791006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106246697 | AAGTGCTGAGAGGTA[C/T]AAATCTCAAAACAGT | 9474 |
rs555879065 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249762 | TAGTCCACATCCTTG[C/T]CAATGCTTGCTACTA | 9474 |
rs555879121 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292047 | GAAAGAAACTCAGAC[A/G]CCTAAATGACTTTTT | 9474 |
rs555916501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106299413 | GGTTGGTTGAATCCA[C/T]GGATGCAGAACCCAT | 9474 |
rs555921677 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106279983 | TAACTTAAAAATCTT[C/T]AGCTATTTGGCCCAT | 9474 |
rs555960154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287752 | CCTTTTTTAAAAATT[C/T]CATGCACTGTTCTCA | 9474 |
rs556002062 | in-del | -/TAAA | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106192613 | TAAAAGCTCATACTT[-/TAAA]TATGGAGTAGAAGTC | 9474 |
rs556019966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106308171 | GAATCTGTCCAGTCA[C/T]CCATGCATCCAAACA | 9474 |
rs556023163 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222595 | TGTGTGTGAAAACTG[A/G]AGAACAGTCTCAAAT | 9474 |
rs556035926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201471 | AGTTACAAAATTAGC[A/G]CCATGAAACAGGTCA | 9474 |
rs556069685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106193974 | TTGGGAACAGTCAGG[C/T]TAATTCATTTAACTT | 9474 |
rs556084663 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305352 | CCCCGGTACTCTTCA[C/T]CTATGTCCTACCAAC | 9474 |
rs556119603 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106256749 | TGTATAGTGCACGTA[C/T]CATCAATGGAGCTTG | 9474 |
rs556119623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249247 | CCTGTAACTATTAAT[A/G]GTCACTTCCCACTCC | 9474 |
rs556139320 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206973 | CAATGCAATCTAAAT[C/T]TTAGGTTGACAGACA | 9474 |
rs556153318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223428 | TCAAAAATCCACATA[A/G]GAAGCAATTTAAGCC | 9474 |
rs556154515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256196 | ATACAAATCCTTTAT[G/T]CTTCTGGAGAGAAAG | 9474 |
rs556167319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322938 | ATTTTATTTTATTTT[G/T]AGACGGGGTCTCGCT | 9474 |
rs556179726 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186301 | AGACCTTCAGTGGTC[C/T]GGTAAGTCTTTCATG | 9474 |
rs556186816 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106201628 | AAAATGAGAAAATTA[-/T]TTTTTACCATTTCTG | 9474 |
rs556187580 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184954 | ATACAAGTCAGTGGA[-/T]TTTTTATCCTTACAT | 9474 |
rs556231485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106257606 | TTCAAATTCTGGTTC[C/T]ACCTCTTGGTAGTTC | 9474 |
rs556328572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106229213 | TAAGGAAGCTCTATG[C/T]TGCGCCCTTAGGCAT | 9474 |
rs556338431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106278556 | CCTCAGTAAGTTCCC[C/T]TGGCTGCATAATCTA | 9474 |
rs556368588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213618 | TCTGAGAAATCAGTG[G/T]ATAAGGAGAGAAAAG | 9474 |
rs556373192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251273 | CAACTCTGGCCTGGC[A/G]GGAAGAGGGAACTTT | 9474 |
rs556376301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265279 | ACATAATGGTAAAGG[C/G]ATCAATGCAACAACA | 9474 |
rs556409137 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216211 | CCAAAGGTTTAAACG[G/T]GGAATTACCATGCAA | 9474 |
rs556451361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235015 | GAAGAATGTTGTTAT[C/T]ATGTTAATCAATCCT | 9474 |
rs556475728 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185779 | GCAAGAAATTCTATG[A/C]CAGCTTCTGAGACAA | 9474 |
rs556509674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106253459 | CAAATTCCTGGACAA[C/T]TGTGACCTGGACAGT | 9474 |
rs556520485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223866 | CATCAAACAATAAGC[C/T]AAACAATGTACAAGT | 9474 |
rs556549095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298884 | AATTAAAGGTACTGA[A/G]TTTCTCTTACACTTT | 9474 |
rs556568408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214320 | GAGGGGGAACAGAGA[A/G]GGGAGTGGGTGGGAG | 9474 |
rs556584034 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210227 | TGATCCTGATGAAAT[A/G]TTTTCTCCATCCTGG | 9474 |
rs556609171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106307244 | CTTCATTTTAATATT[C/T]CCCGATTCAGAGAGC | 9474 |
rs556633595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314229 | ATGAAATTTCTCTAA[C/T]TTTAGGAAGTATGTC | 9474 |
rs556657647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218074 | GTGACAATTTATCCA[A/T]CTGAGAAATGCAAAA | 9474 |
rs556680893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106293544 | CAAATCACCTATTCT[A/G]TGGTTATTACCATTA | 9474 |
rs556683076 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106243215 | TTAAAATATTAATGG[C/T]GCTTTAATGATACAA | 9474 |
rs556683085 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207041 | GATCTTGCCACATAT[C/T]TGTAAATATGCAAAG | 9474 |
rs556709908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306544 | AATGTACAGGGTAGC[A/C]CACCACAACAAAGAA | 9474 |
rs556717469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286988 | ATGCCCAGAATCCTG[A/C]CCCACAGAAACTGTC | 9474 |
rs556726686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211222 | CAAAGTGATAAAAAG[A/C]TATGAAAGAGAAAAA | 9474 |
rs556733316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274890 | AACCATATAACTATA[A/C]CAGAGTGTGATAAAA | 9474 |
rs556749256 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206570 | CAGGAGAATCACTTG[-/A]ACCCAGAAGGCAGAG | 9474 |
rs556796530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311472 | AGTCTGGGTGTGTGT[A/G]GGTATGGGAGATACC | 9474 |
rs556822149 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327480 | CCCAGGTAAGAGGAT[A/T]GCTTGAGCCCAGGAG | 9474 |
rs556823926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207690 | AAATCAGACAATGTA[G/T]GGACTTTAAGAGTAA | 9474 |
rs556826667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106193168 | TTACAGGGCTTTTAT[C/T]CTATGATCACAAACA | 9474 |
rs556830777 | in-del | -/AAC | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106270890 | CTCTACATCCAGCCT[-/AAC]AACAGGCTCTGCCAA | 9474 |
rs556837464 | snp | A/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185533 | TCAAGAGACAGGTAA[A/T]CTTTAAACTTCAAAA | 9474 |
rs556848906 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255972 | GTTATTTCTCTTGGC[C/T]GAAATTAGTTTATTA | 9474 |
rs556872309 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205001 | AATGAATAGGGAACT[A/G]TAGTGATAATTTAAA | 9474 |
rs556875825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283911 | ACAAAGTTATTTATT[C/T]AATTAATATAAATGC | 9474 |
rs556883773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106299297 | ACAATGTAAGTGCTA[C/T]GTAAATAGTTGTTAT | 9474 |
rs556892118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106261949 | TCAAAGAATTATCCA[A/G]TCCAAAAAAGTCAAC | 9474 |
rs556902144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199917 | TACTATAAAGGCTAG[C/T]AAAGTTCAAGGAAGA | 9474 |
rs556910897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290966 | ACAACAAATACTATC[A/G]CTTGTTTTCCCTGCA | 9474 |
rs556936663 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230104 | CTCCCAAATGACTGA[A/G]GAAAAAACCACAATG | 9474 |
rs556968361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195067 | CCTTAGCCATTTACA[A/G]AAAAAGAAAGGAACA | 9474 |
rs556998384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310475 | AAAGACATCATCTTC[C/T]TGTCTTTTACCTGCA | 9474 |
rs557010951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106288585 | CTACAGACAATTACC[A/G]TTAACTTTTAGATCT | 9474 |
rs557025747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301785 | AAATCTGAAAGACTC[C/T]GGTCCCAACCATTTT | 9474 |
rs557064161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260184 | TATGGGTGCAGCAAA[A/C]CAACATGGCACATGT | 9474 |
rs557074309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106232664 | GGCCTAGTAAAAGCA[C/T]GCAATAGCCCCTACA | 9474 |
rs557082405 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269974 | ACCTCTCATTAGTAT[A/T]ATCTGTATTGCACTG | 9474 |
rs557083938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236141 | TTACTCAATGTAATG[A/T]TCTGTGACATTTATC | 9474 |
rs557091375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225293 | ACTGATGCATGTCAA[A/G]GATTCAATTCATTCA | 9474 |
rs557134083 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321297 | CTCATATTTCCATGG[C/T]CCCTCTGCTTGAACA | 9474 |
rs557147395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287922 | GGCAAAATGTTAAAA[A/G]GCAGCAAATCCAAGT | 9474 |
rs557165679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294308 | GTAACTCTGACCAAG[A/G]TTCAAATATCAGTTA | 9474 |
rs557167953 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200893 | CATTTTACACACACA[A/C]ACACACAATGTGGTC | 9474 |
rs557195580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323239 | TCTGTGGTCTTTTCC[A/G]TTTCGCTAAGTGGAA | 9474 |
rs557226051 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106224702 | CAAAGATGGAGAAAC[C/G]CTGTCTCCCCTGTCT | 9474 |
rs557281497 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106315021 | AAACATTCATGCACC[A/G/T]AGTAGTACCACTTGA | 9474 |
rs557290984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106237017 | AAACTAATTCTTGAG[C/T]CTCTGGTTTGAAGAA | 9474 |
rs557294763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265994 | CAAGAATAATTAAGA[A/T]CAGAGCAGAATTGAA | 9474 |
rs557305883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260092 | GCAGGGAACATCACA[C/T]ACTGAGGCCTGTCGG | 9474 |
rs557320989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106188309 | CCGGTATAATTCTCT[C/T]CATATTCTTATATTT | 9474 |
rs557344515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259380 | AGTAAAAATAAGAAT[A/T]AAGTTATTAAAATTT | 9474 |
rs557348177 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233492 | TCTTTACATGTCACA[C/G]AAAAAAACAGAAATA | 9474 |
rs557361807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106288524 | AAAATACAAAAATGC[C/T]TATAAAAATATTAAT | 9474 |
rs557366514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231453 | CAGTGTAGACCCTCA[C/T]TGGGACACAGAATCA | 9474 |
rs557390031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106281205 | ATAAACTTTTTTAAA[A/G]GTCAAACTTATGATT | 9474 |
rs557397726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244793 | ATGTGTGTAAATAAA[C/T]TTGTTGAATGAATCA | 9474 |
rs557411375 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106297011 | TACTCTAGACTTTAA[-/T]GACAATAGTGAAATT | 9474 |
rs557425692 | in-del | -/A | 0.0196059 | 0.0970493 | intron-variant | ATG5 | GRCh38.p7 | 6:106242630 | ATAAATAACAACAAC[-/A]AAAAAAACACCTCAA | 9474 |
rs557486713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266554 | ACACAACAAAAAAAG[A/C]AAATTTCAGGCCAAT | 9474 |
rs557507194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106217996 | GCTTAACTTATGATT[A/G]TTAAACAGGGTTCTA | 9474 |
rs557517377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302129 | CCACAAAAAAGGTCA[C/T]AGTTAAGCTAGATGT | 9474 |
rs557517596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266770 | TGATTCTCTCAATAG[A/G]TGCAGAAAAGGCCTT | 9474 |
rs557532679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244191 | AGCTTCTTGTTTTTT[A/T]AAAACTAAAAATAAC | 9474 |
rs557540784 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313667 | GGATATAGGCGGAAA[A/G]ATTATGCACAGAGGC | 9474 |
rs557574521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317494 | GTCAACTGGATGCAA[C/T]GTCATCTACAGGTAC | 9474 |
rs557578051 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317317 | ATAATCTATCACAAT[G/T]TAGCCTATGAAAACA | 9474 |
rs557610041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106273595 | GGGAAGGGAATTGGG[A/G]AAGGGGTAGAAAAGA | 9474 |
rs557615011 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106203409 | GACATTCCATATCTC[-/TT]GAGTTTGTTGTGGAA | 9474 |
rs557629249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296445 | ACATGATGCCTAGAA[A/G]GATGATAGAAGAATG | 9474 |
rs557633309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246597 | ATTCCTAAATTAAGT[A/G]TAATACATTTTCCCT | 9474 |
rs557648889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272851 | AAGACTTGATTAAAC[A/T]TGAGAGTATAAAATC | 9474 |
rs557659514 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282403 | TTACTAGGTTCCTGT[C/T]TTTTTATCAGTGTAA | 9474 |
rs557662936 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281281 | TTGACAATGAGTAAC[C/T]GTCAGCCCAAGTATA | 9474 |
rs557667779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252747 | ATTCAGCTGGCTAGG[A/C]CCCTCATGCAGGAAA | 9474 |
rs557683765 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303764 | AACATCAAAAATCCA[C/T]AAATGTCATCTATTA | 9474 |
rs557761485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202625 | ATTCATTGTTCAAGT[A/G]TTTAGGAAAGAAGTG | 9474 |
rs557786176 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259722 | CTTACATAAAAATAA[C/T]GACTTTTAAATACAT | 9474 |
rs557798273 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106208913 | TATAGGTGGCAAATA[A/G]GCATATGAAAACATA | 9474 |
rs557816906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308683 | ATATTTCTTATGGGG[C/T]CATTACTTTAAGCAC | 9474 |
rs557826695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209783 | GGGAAACTAGATGAA[A/G]GGTATGTAGATCTTT | 9474 |
rs557834726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310320 | CTGTTCCGTTTGGCC[G/T]GTGGGAGTAATCTTT | 9474 |
rs557835099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208426 | TCTAATTTAATACTA[C/T]GCAAACTGTGTTCAC | 9474 |
rs557868638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243459 | CTTGAGCCGGGAAGG[C/G]AGAGGCTGTAGTGAG | 9474 |
rs557873941 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261547 | GCACAGCTGTTGTGA[C/T]GGCAGTGATAATTCA | 9474 |
rs557892479 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106230929 | ATTAAGAGACAACTC[A/G]CAATTATGTAAAAAG | 9474 |
rs557895385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194041 | CCAGAAGCATCTTCT[A/G]TCAGTCCAGTAATGT | 9474 |
rs557897873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309709 | AGAAAAGATTCAGTG[C/T]AGTCTTTCAGAAATG | 9474 |
rs557934481 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106245652 | TCCGGTTATGCAGAA[A/G]TTCTATTAGGATTCT | 9474 |
rs557947529 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264121 | ATAGGAAATGCTAAC[A/T]AGAATAACCCGTTTT | 9474 |
rs557955761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300005 | TTACTCTATATGTAG[A/G]ACAAACACAAACAAC | 9474 |
rs557960962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196071 | TACGTGTCTGATGTT[C/T]ATAATCACCATTTAA | 9474 |
rs557963737 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201446 | CTTGCAGGAAAACAG[C/T]CTTAACCTAAGTTAC | 9474 |
rs558012644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252765 | CTCATGCAGGAAACC[A/G]ATGAAATGGTCTCCA | 9474 |
rs558017430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236825 | TATTATATGCCCCAT[G/T]AAAGCAAACACAGTG | 9474 |
rs558024579 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310161 | CTGCCCAAAATAGTG[C/T]CTGCTTTAAAGGAGG | 9474 |
rs558029783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230376 | TACTCAGGAACTCAG[C/T]CTAGCTCTAGGACTC | 9474 |
rs558030418 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106224139 | GGAGCCAAGGCTATT[C/G]CCAGGAGTTAACAGA | 9474 |
rs558051698 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106203811 | CCTCATATTTTATAA[A/G]AATATGACTTCAAAC | 9474 |
rs558057222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295924 | CATAAGACTCAATCA[C/T]AAATTATTTTTTTAA | 9474 |
rs558086564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210208 | GCAGGAAAAGCCCCT[C/T]AGGTGATCCTGATGA | 9474 |
rs558108715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106207577 | ATGAAATGCAAAGAA[A/G]AAGTCTCTATTTCAA | 9474 |
rs558124724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194409 | GCATGAGATTTATAT[A/G]TTTCTTTTTCTAACT | 9474 |
rs558135185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251170 | ATCTGTGGTTTCCCA[C/T]CCAGCTGCCACTCCC | 9474 |
rs558158815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106198701 | AGAATCACTTGAACC[C/T]GGAGGTGGAGGTTGC | 9474 |
rs558201653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206242 | GTAAGGCTTTTGCCC[C/T]TTCTGCCATGTTGGG | 9474 |
rs558218308 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106260618 | TGGGTAAAAACCTTG[A/C]AATTCTCTGAATGCT | 9474 |
rs558219792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106305523 | GACAAGGTTATAAAG[A/G]GAGAAGAAACATCAA | 9474 |
rs558232768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240670 | AGTAAGCTGGCAATT[G/T]TTTTTTTAATCTCTA | 9474 |
rs558261170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191532 | AGTTTTGAATTCTCA[A/G]GCAATTCACTCAAAC | 9474 |
rs558274111 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233028 | TCTCATACCTGGGCA[C/T]TCTTGTCCTTTGGTA | 9474 |
rs558291226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228507 | TATAACACTCACCGC[A/G]TGGCCCAAGATTCCA | 9474 |
rs558306319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106291847 | ATGTGCTCTATCTGT[A/G]CTGTTCTTTGGTAAC | 9474 |
rs558319114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272740 | AGGTTCTTATACTGG[C/T]TAGCTAATCCACACT | 9474 |
rs558323476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258212 | CGTCTCTAACAAAAA[A/G]AAAAAATTAGCCAAG | 9474 |
rs558341820 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316417 | TTTAGTATAAATTCA[-/AAG]AAAAGAGTACAACAA | 9474 |
rs558370829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323181 | TGACCTCGTGATCCG[A/C]CCGCCTTGGCCTCCC | 9474 |
rs558393626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298089 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 9474 |
rs558435464 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326735 | AGACTCAAAACAGGT[C/G/T]CTTGATAATTGGGAA | 9474 |
rs558454715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280135 | ATGGAGCCCTCACAC[A/G]CTACTAACAGAAATG | 9474 |
rs558455834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288324 | TAAAAAACTGGGGAC[A/G]CAGAAATGAGATAAT | 9474 |
rs558461253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106269551 | CCGAGCCCTGCCCCG[C/T]GGGAAGGCAGCTAAG | 9474 |
rs558514164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320426 | TCAATAAAGGTATTA[A/C]GTGGGCAGGTGCAAT | 9474 |
rs558517120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275412 | TCTCTCACAAGACTA[C/T]TCAGTCTTAGAAGTA | 9474 |
rs558555379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190671 | GAACATAAAAAAAAA[A/G]TTACGTTTTAAGAAA | 9474 |
rs558591915 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106283067 | AAGTACTGGGATTAC[A/G]GGCATGAGCCACTGC | 9474 |
rs558608616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106297569 | TGCATTCAGGGGATG[C/T]TGACCATTTTAGATA | 9474 |
rs558633130 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238923 | AAGCATAAAAAAAAG[C/T]GGAGGGGGGGAACCC | 9474 |
rs558692412 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323565 | TTTAGTTGCTCAGTC[C/G]GTAACCCTTGGAGTC | 9474 |
rs558723380 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ATG5 | GRCh38.p7 | 6:106325354 | CAGGGCTCCGGGCCG[C/G]CGTCTCGCCAACTCC | 9474 |
rs558728364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255029 | TTTTCAACCACCATA[A/T]AAGGTTCTATCTTCT | 9474 |
rs558734873 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184331 | CAAATAGGCATATTG[G/T]GGGTCTTCTCCAATT | 9474 |
rs558742056 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272842 | GTTGTTTCCAAGACT[C/T]GATTAAACATGAGAG | 9474 |
rs558745010 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269037 | TGTATCCTAGAACTT[A/T]AAGTAAAATAAAATA | 9474 |
rs558745539 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189367 | CCCAGCACTTTGGGA[A/G]GTCAAGGTGGGAGGA | 9474 |
rs558784506 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106290221 | TTATTTTATTTATTT[A/T]ATATATTTTATTTTA | 9474 |
rs558811001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238790 | TTTGAAATAGGGGTA[A/G]AAGAATAAAGGGTCT | 9474 |
rs558814445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277326 | TGGACTAACTCCCTG[A/G]CCAAAAACACTGTTG | 9474 |
rs558843006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106266464 | AACTATTCCAAACAA[C/T]AGAAAAAGAGGGACT | 9474 |
rs558850109 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270632 | GATTCTAGTCTATTA[C/T]GCATTCTCCATCTGC | 9474 |
rs558851017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291346 | AAACAATGACAACTA[A/G]TACAGTGAGGTACAA | 9474 |
rs558854893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285196 | CATCTTTAATTTGCT[A/G]TTAAGCCCATGTAGT | 9474 |
rs558855328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106276442 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 9474 |
rs558887058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231912 | GGAAAAGGGAAAAGC[C/T]AGGCAAATCAAATGC | 9474 |
rs558900378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267509 | AATTTCATATGGAAC[C/T]AAAAAAGAGCCTGTA | 9474 |
rs558934551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267855 | AAGGTGGATAAAAAG[A/T]CTTAAATGTCAAGCC | 9474 |
rs558935783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238396 | ATATTACTGTAACAT[A/G]TATCTCTAAATGAAA | 9474 |
rs558949583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318204 | GGAATAGTAATCTGA[C/T]TGGTCAGATTCCAGG | 9474 |
rs558954305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226166 | AGATACTCTAGTTCT[A/G]GGCATTCAAGAAAAT | 9474 |
rs558960397 | in-del | -/GAGAG | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106229432 | AGAGAGAGAGAGACA[-/GAGAG]GAGAGAGAGAGAGAC | 9474 |
rs558963575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318666 | CCAAGGCAGCTAAAG[A/G]TATAATGTAGTAGAG | 9474 |
rs558971792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219873 | TATGGTCTACTCAAA[C/T]ACGGTTTCCAAATGT | 9474 |
rs558975870 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298817 | GATTGCTTATTTCTA[A/G]TGAATCTACTGATAT | 9474 |
rs558991465 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245211 | TTTACCACTAAAAAT[C/T]GGTCACCTGACTATA | 9474 |
rs559001785 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322092 | TCAAGGAACTGTCTT[A/G]GAAATAAAGAAACTC | 9474 |
rs559009650 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191768 | ATAAAGTATGTGAGG[A/C]CAGAAGATCATTTTA | 9474 |
rs559039840 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ATG5 | GRCh38.p7 | 6:106188596 | AAGGCAAAAGACCAA[C/T]CATGTTACAAAAGGA | 9474 |
rs559059920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237508 | TGTCTGGTCATTGAC[C/T]TCCAACTTAAAAAAT | 9474 |
rs559074019 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241042 | CCTGTAGTCCCAGCT[A/C]CTCAGGAGGCTGAGG | 9474 |
rs559093125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232466 | CCCGTTTGTTGTCCC[C/T]TGCTTGAGGAAGGAA | 9474 |
rs559095566 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260242 | TGCACATGTACCCTA[A/G]AACTTAAAGTATAAT | 9474 |
rs559130370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106231745 | AAAAGTCTGCCTTAG[A/G]CCCGGAACAAAACTT | 9474 |
rs559147568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196442 | TAAGTGGTTAAGAGA[C/T]GTTTGGCACAATCAT | 9474 |
rs559151952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267578 | GGCATCATGCTACCT[A/G]ACTTCAAACTATATT | 9474 |
rs559180645 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296543 | AGCATGCAGGCTGGG[C/T]GTGGTGGCTCACGCC | 9474 |
rs559188985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211370 | AGTCTCCTACGGACA[C/T]AGCAGGCAGAATGTA | 9474 |
rs559236234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219438 | GGGGTTCTGCATCTG[C/T]AGATTCAACTAACCA | 9474 |
rs559249059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232776 | TCCCTCTATACCTAG[C/G]TGTACCTAACCCTTA | 9474 |
rs559273468 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106216831 | GTACTGCACTATGAT[A/C]ATACCTGTAAATAGC | 9474 |
rs559287781 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184733 | TACTGCAAAGGCCTG[A/G]CACTGGTTTTGTCTG | 9474 |
rs559316091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323252 | CCGTTTCGCTAAGTG[A/G]AAAAGTCCTTTTTTT | 9474 |
rs559316714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226722 | GTTGTGTGAGATTTA[C/T]CCATGTTGTTGCATG | 9474 |
rs559321229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106324131 | TACACAGTTGGCCCT[C/T]CCTACCCATGGGTTC | 9474 |
rs559328114 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291024 | AGAAAATGTCTAACA[A/G]ATAACAAAGTCTCAA | 9474 |
rs559341717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282503 | TTACTGTACAATTTT[C/T]AATAGCAAAGTTAAG | 9474 |
rs559361196 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286613 | ACTTGCTTCTAACTC[A/C]AAGAATGCGGCAAAG | 9474 |
rs559375806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226418 | AGACATGCAAAGAAA[C/T]AAGTATAAGCCACAA | 9474 |
rs559378539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323067 | GGGACTACAAGCGCT[C/T]GCCACCAGGCTCGGG | 9474 |
rs559384054 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233429 | CAGGCCCTAAAGAAG[G/T]CCCTAACCCAAGCCC | 9474 |
rs559404046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195482 | TTTTGGATACTCTAC[A/G]TAGATTTTTAAATGA | 9474 |
rs559417790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106189310 | GCAATATCAAAACCA[A/G]TAAAAGAAAACAGGC | 9474 |
rs559468934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289935 | TTCAGGCTCACAAAG[A/G]TATGTAGTTTAAAAG | 9474 |
rs559474859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296052 | CTGAATGCATAAATC[A/G]AAGAAGTCCACAGAC | 9474 |
rs559517408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106272940 | AGGAATGAAAAATAA[C/T]AGATGAAACAAGGCT | 9474 |
rs559525503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309404 | TAGGTAGGAGAACGT[A/G]ACATTGATCCTAGGG | 9474 |
rs559624850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225907 | TTAAAAGAAAAACCT[A/G]GGAAATAAGAAATCC | 9474 |
rs559646247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317891 | TAGGTTATGACAAAT[A/T]AGTAAATCTAAAATT | 9474 |
rs559679001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106213065 | TACTACTACTAACAT[A/G]TAAGTAGCCTGGATA | 9474 |
rs559690878 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247064 | TTACTTTCAATTAGA[A/C]AATTTGCTTTCCTCT | 9474 |
rs559704327 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319296 | AAAACTAATAATAAT[A/C]AAAAGCATTATATAA | 9474 |
rs559713466 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304859 | CACTTTGGGAGGCCC[A/C]GGCAGGTGGAGCACC | 9474 |
rs559713727 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239327 | TAAAATCTATGCAGA[A/G]CATAAAACAAAATCT | 9474 |
rs559741348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303294 | TATAAACAACTCTAT[A/G]TTCATAAATTAACAA | 9474 |
rs559751787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106313704 | TCAAAATGCAGAAAA[A/G]AGGAATATATGTACT | 9474 |
rs559772804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258895 | TTAGAGATGACAGAA[C/T]AGCACAGCTAGCAGT | 9474 |
rs559774772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266064 | AATGAATCCAGCAGC[C/T]GGTTTTTTGAAAAGA | 9474 |
rs559776069 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106250146 | CTCTATAAAGCAAGG[A/G]AATACATCCAGAATT | 9474 |
rs559780781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319870 | TTGTTGGAAAGACAG[C/T]GTATGAATATAAAAC | 9474 |
rs559815137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265588 | TGTGTATTCTAAAAT[C/T]GACCACATAATTGAA | 9474 |
rs559824159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230538 | AATCCGATAAGCAGA[A/G]GTCCATGGGTGGTTA | 9474 |
rs559828110 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222093 | GACAGGGTTTCACCA[C/T]GTTAAACCATGAGTT | 9474 |
rs559873645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245327 | TACCACCAGTCACAG[A/G]TATTCTAGGCTCCTA | 9474 |
rs559912212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252488 | ATGTTATTTTTTTTT[A/T]AATTTCAGAGCTCTC | 9474 |
rs559971416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106309896 | TAGTAATCTATTCTG[C/T]AGAAAACAATATTAA | 9474 |
rs559993955 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | ATG5 | GRCh38.p7 | 6:106207536 | AGAGACCTCATCTCT[A/T]AAAAAAAAAAGAAAG | 9474 |
rs559998186 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242181 | GACAGGGTTTCACCA[C/T]GTTGTCAAGGCTGGT | 9474 |
rs560005527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302422 | GGGTTCTTGAGGACA[A/G]TAACAATGTTAGATC | 9474 |
rs560026641 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106228205 | TTAAATCTTGCAACT[G/T]CACTCTTCTGGTCCG | 9474 |
rs560031734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213722 | CCAACTCCCAACAAC[A/G]TACTGTGTATCTAGA | 9474 |
rs560037963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106206779 | AGTACAGAGGTTCTT[A/G]AGGGCAATGGGAATG | 9474 |
rs560040773 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106259611 | TCCCTTCATCACCTT[G/T]TCTCTTCTGCTCCTT | 9474 |
rs560047297 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106325159 | GAGGACATACCCACC[A/G]AGTTTGGACAGACTC | 9474 |
rs560067237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241975 | TTTCTCTGGAGAATG[C/T]TAATACACCCCTGTT | 9474 |
rs560078280 | in-del | -/AAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226001 | GCTGTGTACACGCTC[-/AAA]AAACATCTACGAAGG | 9474 |
rs560085242 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106208671 | ACTTAATTAAAATTA[-/AAC]AACAACAACAACAAC | 9474 |
rs560089842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320715 | TTATCCCTCTAATGT[C/G]AAATCTATAAATGTA | 9474 |
rs560091010 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305092 | CAAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 9474 |
rs560127189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106303828 | CATATAATTAGCACA[C/G]AAAAGGCATCTGACA | 9474 |
rs560131049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200104 | CATTACATACATGTA[A/G]GAATGCTAGTATAAG | 9474 |
rs560166162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106262121 | TCTGTCACCCAGGCT[G/T]GAGTGCAGTGGCACC | 9474 |
rs560179005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106263238 | TGGGAGGTCTGGACT[A/G]AGCGGAATTCACCAC | 9474 |
rs560182103 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ATG5 | GRCh38.p7 | 6:106228572 | CAGAGAACACGAGGC[G/T]TGCCATCATCTTAGA | 9474 |
rs560183207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255645 | AATAATTTATTTCAA[A/G]TGTATTTTTAAGCCA | 9474 |
rs560199951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106299094 | TAATAGAAAAGCAAG[C/T]AGTAAGGATTTGAAC | 9474 |
rs560213643 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190317 | CGTGGAAGTGTGAGA[C/G]ACAGTGAACCCACTC | 9474 |
rs560253053 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284152 | ACGCAAGTTATTTCC[C/T]TATTTTGCATATCAG | 9474 |
rs560265407 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324150 | ACCCATGGGTTCTTC[A/G]TCCTTGTATTCAACC | 9474 |
rs560284589 | in-del | -/AGTCG | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106201774 | GTATTTTATTTCGCC[-/AGTCG]AGTCATCATTTTGTT | 9474 |
rs560291498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197531 | TTTGGGTTGGGGTGG[C/G]GGGGGCGGGGGTGGA | 9474 |
rs560344741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299610 | TCCATATTCAATTCT[C/T]GAAATGAATATATTT | 9474 |
rs560353522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284786 | ATCTTTTCATGTGTT[G/T]ACTGGCCATTTATAG | 9474 |
rs560390391 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106291916 | ATAATAAATGTACAC[A/G]GAAATAAGCTCTAAT | 9474 |
rs560401094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256987 | CAAACACGTACAGCC[A/G]CATAAAAACATTTTT | 9474 |
rs560439737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106256468 | GATGATTCTAATATA[C/T]AGCCAGCGTTAACAA | 9474 |
rs560447996 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193318 | ATACCAAATACCAGA[-/T]TATACCACATATCTC | 9474 |
rs560503284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220355 | ATGCACTGCAAAGCA[A/C]AAGTATAATATAAAA | 9474 |
rs560540970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319140 | ACTTACCACATTAGA[C/T]ACAAGAATTAAATGA | 9474 |
rs560544993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312462 | GTTTGGAGCTCTGGA[A/G]AAAAATATTGGGAAT | 9474 |
rs560546852 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214087 | CAGACTTTACCAACA[A/G]TGACACATGATATCT | 9474 |
rs560547212 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106205101 | GAAGTAATGTTGGTG[A/G]AAGGCTTTTTCTGAC | 9474 |
rs560549742 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326293 | TTGTAAAAATAATTG[G/T]GGCCGGGCGCGGTGG | 9474 |
rs560551266 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326432 | TACAAAAAAAATTAG[A/C]CGGGCGCGGTGGCGG | 9474 |
rs560584065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253943 | AAATACCTCTTCCCC[C/T]AGAAGCAGATTCCTA | 9474 |
rs560584099 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106211529 | GCCTGGCCAACATGG[C/T]GAAACCTCATCTCTA | 9474 |
rs560589027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190871 | ATATAGACATAGATA[A/C]AATGACTGTTATCAA | 9474 |
rs560610121 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325758 | AATACAACCGGCAAC[A/G]CTGCGGAGCCCTGGC | 9474 |
rs560614600 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325909 | GCATGCGCCAACGGG[A/G]CAGTACGCTTGAACT | 9474 |
rs560629080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198228 | AAAAAGTTTACTTAA[C/G]TATCTCTAAAGATAT | 9474 |
rs560647163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106297060 | TCAAACTCTGAGTCT[C/T]TAGATGATATCTTAA | 9474 |
rs560661001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190763 | AATAAGAAGAAAAAA[C/T]AAAAATCACATTAAC | 9474 |
rs560680230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233551 | AGCTTGCAACCCATG[A/G]CATACCTGAGTAAGG | 9474 |
rs560712386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106227359 | TCAGTATTTTGGGTG[A/G]CCAAGGTGGGAGGAT | 9474 |
rs560775577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276231 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 9474 |
rs560827321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106284150 | GGACGCAAGTTATTT[C/T]CCTATTTTGCATATC | 9474 |
rs560831668 | in-del | -/AAAAG/AAAG | 0.0406909 | 0.137433 | intron-variant | ATG5 | GRCh38.p7 | 6:106207543 | CATCTCTTAAAAAAA[-/AAAAG/AAAG]AAAGAAAGAAAGAAA | 9474 |
rs560891424 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214889 | AAAAGAAGCTTCATA[C/T]AAAAGTGCTAGGATT | 9474 |
rs560900930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268466 | ATTGTGGAACAGTGT[A/G]GCAATTCCTCAAGGA | 9474 |
rs560936499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106276193 | AACTGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 9474 |
rs560948530 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230453 | TAGAATCCAGCAGCC[C/T]GGACCCCTTTCTTTG | 9474 |
rs560986397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262743 | CATTCCTTCACCCAG[C/G]ATGTGCAAGAAGCCA | 9474 |
rs560992898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304142 | CAGAACACAAAAATC[A/G]ATAACATTTTCCATA | 9474 |
rs560996602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312987 | GGGTCAACAGAAGGT[C/T]GTTGTTTCAGGATAG | 9474 |
rs561003555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267554 | CTAAGCAAAAAGAAC[A/G]AAGCTGGAGGCATCA | 9474 |
rs561029618 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277698 | ACATGCTTGTAATCC[C/T]AGCTACTCAGAAGGC | 9474 |
rs561032567 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106305984 | AAACACTAAAGGAAA[A/C]GATGCATCAAAAGTC | 9474 |
rs561068251 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301312 | CAAATGTATTGAGTA[C/T]TCATTATAAGTATAC | 9474 |
rs561107693 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322254 | TCATTCAGAAAATGG[C/T]ACGGTGTGACAACAA | 9474 |
rs561111639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298333 | ACGACAACTCCTTTG[C/T]CTTGGCATATTAAGA | 9474 |
rs561167180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211491 | TGAGGCGGGTGGATC[A/G]TGAGGTCGGGAGTTC | 9474 |
rs561188831 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106191860 | TATAAGAATAAGTTC[-/A]TTTTTTTAGTACTAG | 9474 |
rs561194424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198124 | CAGAGAAAATGAACT[A/T]AAAAAGTAAGCTTAT | 9474 |
rs561194663 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106190234 | TCACAGTTCTGGAGG[C/G]TGGAAAATCCAAGAT | 9474 |
rs561234688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311943 | TCAAGTGATTCTCCT[G/T]CCTCAGTCTCCCAGG | 9474 |
rs561238272 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299196 | ATGCTTAAACCCTTA[C/T]ATTAAATGGCATAGT | 9474 |
rs561358826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253197 | AAAAGCAGGTTTTCA[A/G]TAAGTGACCTGTATC | 9474 |
rs561385015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218438 | AACATTTTAAAAACA[C/T]TCTAAAGCAACAAAA | 9474 |
rs561390311 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302400 | TAGATGATGGTAAGT[C/T]AGAATAGGGTTCTTG | 9474 |
rs561395855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106260499 | TTCTTAAGTAGAAAA[A/G]CACTTTGAAGACGAT | 9474 |
rs561404088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106310947 | CCTCATTTAGCCCTA[A/G]TATAAAGTATTCCAT | 9474 |
rs561412031 | in-del | -/AAGT | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106214757 | ACGTGTGGTACAGAG[-/AAGT]AATACTTCCCTTTCT | 9474 |
rs561412199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210736 | CTTCTTGTGTTACTT[A/G]TGTGTCAATTGTATC | 9474 |
rs561455902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299750 | GAAGGGACATGATTC[C/T]AGTATAAATATCTGT | 9474 |
rs561553737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250011 | CCCCTTATCTATGAC[C/T]CACATATTTTCTCCC | 9474 |
rs561574434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106186757 | CCTTTTGAGAATCCT[C/T]AGTGCATTAAATGGA | 9474 |
rs561588617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257297 | AACACTCTAAAATAA[C/T]GAAAAAAGTAAATAG | 9474 |
rs561589640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288042 | GTGGCATGGTCTCGG[C/T]TCACTGCAACCTCCG | 9474 |
rs561604150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106208083 | GGCAACAGAGCAAGA[C/T]TCTGTCTCAAAAAAG | 9474 |
rs561608780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106290728 | ATGGATCTTTTTACA[C/T]ATGCATGATCTTGTA | 9474 |
rs561614480 | in-del | -/A | 0.0707826 | 0.174302 | intron-variant | ATG5 | GRCh38.p7 | 6:106239163 | ATGCAATAAAGCAAG[-/A]AAAAAAAAAAGTTTG | 9474 |
rs561621133 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243799 | TTGCACTAGTGCACT[A/C]CAGCCTGGGCGACAG | 9474 |
rs561627897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287377 | TGGTAAGCAAAACAG[A/G]ATTTGCCTGCTGTGC | 9474 |
rs561696604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230071 | GAACTCCCTTCAGGA[C/T]AGGATGATAGATGGT | 9474 |
rs561709935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250810 | CTGGAAAAAGAAACA[A/T]GATTGTGCCAGTTAT | 9474 |
rs561735624 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106315276 | CACAAATACACTTCT[A/G]CTTTTCCACATCATC | 9474 |
rs561746021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215560 | ATTTTACAGATTTCA[A/C]CACTTACGTAATCTG | 9474 |
rs561758692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194509 | CAAAGGAGAAAAAAA[G/T]GTGAATATACCATTT | 9474 |
rs561769491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300193 | TTCCATTATTGGAAC[A/G]CTAAGCTTGTGGGAG | 9474 |
rs561784703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106214724 | CTTTGTTTCCTCTTC[A/G]TATCCTTTGACTGAA | 9474 |
rs561828571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308206 | GCAGAAATATTTTCA[A/G]TAACGTATTCTAGTA | 9474 |
rs561839220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236320 | AATGTTTTCTCGGAC[A/C]TATATTTTCATTTTT | 9474 |
rs561839442 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253173 | AGTAGTAATTACTGG[C/T]AGGCTGCCAAAAGCA | 9474 |
rs561842519 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212612 | CCACTGCACTCCAGC[C/T]TGGGCGAGAGCCCAG | 9474 |
rs561858705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224346 | AAAGGACCCATGAGC[C/T]AAATCAGTGCAAATG | 9474 |
rs561893689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249332 | TCCAGACATTTCATA[G/T]AAATGAAGTAATATA | 9474 |
rs561929222 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252010 | CACGCCCGGCTAATT[G/T]TTGTATTTTTAGTAG | 9474 |
rs561983389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106285692 | TGTTGTAGCCGCAAA[A/G]CAGTCATAGACAATA | 9474 |
rs562012941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243763 | CTGAACCCAAGAGGC[A/G]GAGGTTTCAGTGAGC | 9474 |
rs562015767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201876 | AGATATGAAAATATC[C/T]TCCTGAAATAACCTG | 9474 |
rs562036607 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254015 | CTCTGAGATCTCACT[A/G]TCTACCTTACTAACT | 9474 |
rs562044271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199114 | GAATCCTTATACACC[A/G]CTGGTGAGACTGTAA | 9474 |
rs562085110 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326990 | CTTCAGTATGTATGT[A/G]GTGTACACTGGATAG | 9474 |
rs562089108 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201119 | GGGAATAATAACAAG[-/A]AAAAAAAGTCTGTTT | 9474 |
rs562112269 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106251702 | AAGACAGAAAAAGAA[-/AG]AGAAAAAGAAAGAAA | 9474 |
rs562126225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191856 | ACGTTATAAGAATAA[G/T]TTCATTTTTTTAGTA | 9474 |
rs562144626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299021 | CACATATACCCTAAG[C/T]AAATCATAACGTAAC | 9474 |
rs562150568 | in-del | -/A | 0.19334 | 0.243495 | intron-variant | ATG5 | GRCh38.p7 | 6:106289402 | ACTTAGTATATACAG[-/A]AAAAAAAAAAAATCT | 9474 |
rs562158708 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226846 | TGAATTAACTTGAGG[G/T]GCTCAACAGCTGATT | 9474 |
rs562176134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106199966 | TAACCTCTTAAATCC[C/T]GTTCAGTTTTAATAA | 9474 |
rs562181200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292162 | ACCAGTTCAAGCACC[A/T]GAGACCAACATGGTG | 9474 |
rs562213119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207526 | GGCAACACAGAGAGA[C/T]CTCATCTCTTAAAAA | 9474 |
rs562218179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222553 | GGGCAGTAAGCAACC[A/G]AAAAGGAAGAGTAAT | 9474 |
rs562247747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277875 | CAAGTTAAAAGAAAT[C/T]CTAATATTTATTTAG | 9474 |
rs562249285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306792 | CTATTTAATAATTGT[C/T]GCTCTGTTTACACTT | 9474 |
rs562271967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228757 | TTGGAGGAAAATACT[A/G]GGCACCTGTCGGCCG | 9474 |
rs562300228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106314569 | CTCAAAATAAATAAT[A/T]AATAAATAAATAAAT | 9474 |
rs562325402 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ATG5 | GRCh38.p7 | 6:106320908 | AGCCAGGTAGTAATT[C/T]CAGCAACTAAGGCAA | 9474 |
rs562390730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106193518 | CCCATATGATCAGTT[A/G]TAATTATAAAAAGCA | 9474 |
rs562398425 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190581 | TTCTTAACCTTTACA[A/G]TTTTGAAGAGTACAT | 9474 |
rs562402395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106263400 | ACCTGGGGGAAGGGG[C/T]GGCTGTGGGTGCAGC | 9474 |
rs562417411 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327429 | GTTGGGACCAGGCAC[A/G]GTGGCTCATGCCTGT | 9474 |
rs562427385 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283398 | TCTTAAATATTTTAT[A/T]TTATTTTTATTTTTA | 9474 |
rs562438908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213798 | ATGAGGAAAACTTAT[A/C]TTTGAACAATTGATG | 9474 |
rs562489672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256560 | AATGCATCAGGCAAT[C/T]TCATCATGCGAACAT | 9474 |
rs562555626 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220766 | TTATGAGAAGAACAG[-/A]AAAAAAAAATTAGAA | 9474 |
rs562560437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248782 | CGTCTCTATTAAAAA[C/T]ACAAAATTAGCCAGG | 9474 |
rs562567816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106321609 | ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 9474 |
rs562587648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286618 | CTTCTAACTCAAAGA[A/T]TGCGGCAAAGGTGAT | 9474 |
rs562597353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106255468 | AATTAATCTTATTAA[A/G]TATTGAGAAAAGCAG | 9474 |
rs562611742 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106242503 | GAGAATGAATGTACA[-/AC]AGTGTGAACATAATT | 9474 |
rs562626029 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299802 | AAGTATTCTAAAATC[A/G]GCACTGAAAGAATTT | 9474 |
rs562642696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243713 | GTGGGCAATTGTAAT[A/C]CTAGCTACTCGGGAG | 9474 |
rs562645363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106193682 | CAATATTATTTTATC[C/T]GCTTTCATAAAATGA | 9474 |
rs562656558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293334 | AAACCTCAATATGCA[C/T]AATAGGATTGTGGGC | 9474 |
rs562677736 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301759 | ACATTCCAAAATCTG[-/A]AAAAAATCTGAAATC | 9474 |
rs562681289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250707 | TTGTCATGAAATCTC[A/T]AGCACCTAGCATGGT | 9474 |
rs562714760 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274268 | ATAAAAATGCTACTT[A/T]CTTTTATTTCTTGTG | 9474 |
rs562721600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241005 | AAAAAATACAAAAAT[C/T]AGTCGGGCATGGTGG | 9474 |
rs562815412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249813 | CATTCTGGCAGGCAT[A/C]AAGAAGTATCTCATT | 9474 |
rs562830465 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276552 | AAAACCAGGCCTTTG[C/T]TGTTCTTCTAACACT | 9474 |
rs562857198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106298298 | TTTTTTTAAATTTCA[C/T]TGGTCCCAGATGGTA | 9474 |
rs562947308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106305780 | TATCCTATTTTGCGA[A/G]GCCCACTACTTAAAT | 9474 |
rs562953176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206558 | AGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 9474 |
rs562953861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245129 | CAAACTAAACTGTTA[C/T]GTAAATGACAGAAAT | 9474 |
rs562979296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297928 | AAATTAGCCAGGCAT[C/G]ATCTGTACTCAACAG | 9474 |
rs563012106 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184107 | TTTTTTTATCCTTAC[A/G]TAACTCAAATATTGC | 9474 |
rs563042019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228685 | CAACCATGAAGGGAT[A/C]TCCAAAGCGGTAATA | 9474 |
rs563063542 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326956 | TGTAAAGGGTAAATA[C/T]TGTGTCCCAAAATTT | 9474 |
rs563104252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234380 | ATCCCTGTACCTGAA[C/T]AATGGAACAACTACA | 9474 |
rs563110914 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310520 | CTCATTGTTTTTCTT[A/G]GGTGTATTTCATTGG | 9474 |
rs563137614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267081 | GATGACATGATTGTA[G/T]ACTTAGAAAACCCCA | 9474 |
rs563149582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283685 | TCTGAGTAGCTGGGA[A/C]AACAGGCATGTGCCA | 9474 |
rs563164582 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233259 | ATCCCAAAACCCTAA[A/G]GCAACTAAGAGGATT | 9474 |
rs563169262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106192483 | ATTCTAGTGAGATGC[C/T]TGAGTTTCCTTCTTA | 9474 |
rs563169439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285528 | TACTGGCAGCTCTCC[G/T]TAATCCTAAAAAGGC | 9474 |
rs563174601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273916 | CCATTAGCTAATCAC[C/T]ATCTCCTCTTAAAAA | 9474 |
rs563222238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203392 | TTTATCTGTTAATTT[A/G]GGACATTCCATATCT | 9474 |
rs563267515 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280340 | CATTTAAGGACTTGC[C/T]ACATGAATGTTCACA | 9474 |
rs563313476 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106223536 | CAGGACTCAATTTAC[C/T]TATTTCTTTTAAAAG | 9474 |
rs563352092 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106294601 | GGTGGGTGGATCACT[G/T]GACTTGAAGTCAGGA | 9474 |
rs563353798 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302256 | GATGAGCAAAGAAAC[A/G/T]GAAGCCCAAAACATT | 9474 |
rs563382177 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308181 | AGTCATCCATGCATC[C/G]AAACAGAAGGCAGAA | 9474 |
rs563443789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289718 | ATAAAACCACTATAC[A/G]TTAACACTAAAATTG | 9474 |
rs563453015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194123 | ATCAAATAGCGTGAA[A/G]GTACAGAGATACTAG | 9474 |
rs563466604 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238291 | CAAGTGAACAAATCA[A/C/T]ACTTTTAAGCACAGA | 9474 |
rs563503189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106230421 | AGGCAATGTTGGGCA[C/T]GCTGGTAAAGGACCA | 9474 |
rs563518613 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106205616 | GCCAACTAGTCTTGG[-/T]TACATATTAAAAAAC | 9474 |
rs563533223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106264949 | TAATGGGCAAAAAAA[A/C]CAGCTAGTATCATGA | 9474 |
rs563546614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189151 | TTCTGATAGCTAGCC[C/T]TACCATGGAGAATAA | 9474 |
rs563568937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224975 | CACTGGTCATAAAAC[A/G]AAAGAATACAGGAGG | 9474 |
rs563630752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231156 | GCCCAGCCAGAGTGC[A/C]CGTACCTTTTTCTCT | 9474 |
rs563639762 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186064 | TGTAATTCAATCTTT[C/T]ACAAAAAATTACTTG | 9474 |
rs563672091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272260 | CCAAAGGGATGTCTT[A/T]AAAAGGGAAATCTGA | 9474 |
rs563702527 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205885 | AAATCTTATTTTAAA[-/AC]ACAAAAACTCAATAT | 9474 |
rs563702611 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226154 | GCAAAGATTGGAAGA[C/T]ACTCTAGTTCTAGGC | 9474 |
rs563702658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106290423 | ATTCCTGGGCTAAAG[C/T]GATCCTCCTGCCTCA | 9474 |
rs563708986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106280441 | TGTGGCATAAACTTA[C/T]TCACTTTGACTAGGT | 9474 |
rs563740379 | in-del | -/AACAA | 0.00119976 | 0.024463 | intron-variant | ATG5 | GRCh38.p7 | 6:106277813 | GTGAAACTTCGTCTC[-/AACAA]AACAAAACAAAACAA | 9474 |
rs563770034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106309818 | AGTATAATCTATTAG[C/T]CTAATAAGGTCTCTT | 9474 |
rs563775563 | snp | C/T | 0.000680052 | 0.0184272 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186633 | AGGTGTTTCCAACAT[C/T]GGCTCAATTCCATGA | 9474 |
rs563812838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287313 | GCTTGCTCAGTCACA[C/T]AAAAATACTCAAGGA | 9474 |
rs563824552 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271572 | CACCTTAATGTAAAC[A/C]GGTCCAATTCTAATT | 9474 |
rs563830505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243442 | CTGAAGTGGGTGGAT[C/T]GCTTGAGCCGGGAAG | 9474 |
rs563915256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301349 | TCTTAAATTTTTTTA[A/G]TTCTAATTTGGACAA | 9474 |
rs563926573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258837 | TCAAAAATTATGGTA[A/C]CATCTGGTATAGTAA | 9474 |
rs563941950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243780 | AGGTTTCAGTGAGCC[A/G]AGATTGCACTAGTGC | 9474 |
rs563973418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315970 | TGCTTATCTGTGTTA[A/T]TTTTTTTTCCAAAAT | 9474 |
rs563987420 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191300 | TACAACACAGGTAAA[A/G]ATATGGCAGCTTTTG | 9474 |
rs563990869 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ATG5 | GRCh38.p7 | 6:106212210 | TTTGTACAACAATTA[C/T]TAAATTTCTAAGTAG | 9474 |
rs563991781 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287790 | CAAAGAGAGAAAAAA[-/T]TTTTTTAATTTTAAA | 9474 |
rs564001365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300399 | ATACACAGGTTTTCA[C/G]TAAAGCATTTTGCTA | 9474 |
rs564012799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280504 | AAGCTGTTAAAAAAG[C/T]AGATTTTAAAGTCAA | 9474 |
rs564014810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288718 | CCCAATGCTGCAGAA[G/T]CAGAAACTGCACTTT | 9474 |
rs564031066 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279966 | CAAAATACTTTAAAA[C/T]TTAACTTAAAAATCT | 9474 |
rs564040112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293946 | AAATGCTTGGGATTA[A/G]AGAAGTGTTTCAGAT | 9474 |
rs564050211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216566 | ATTAGTAGTTGCCAA[A/G]GGCTGGAGGGAGGGG | 9474 |
rs564051490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288124 | TACAGGCACCTACCA[C/T]CATGCCCAGCTAATT | 9474 |
rs564060933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294476 | GCTTACTTGTATAGA[A/G]TTATGGAAAAGTCAT | 9474 |
rs564075250 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106305686 | CTATCCTTAAGACAC[-/T]TTGTATGGTCTCAAA | 9474 |
rs564112636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106229460 | GAGAGACAGGGAGGA[C/G]AGGGAGAGAGACAGA | 9474 |
rs564112955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235517 | TGGATTTCCTAGGCC[A/G]ACTAAGAATCCCAAA | 9474 |
rs564114296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323076 | AGCGCTTGCCACCAG[A/G]CTCGGGTTTGTTTTT | 9474 |
rs564117276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202906 | GAGCTCAGGCAATCT[G/T]CCGGCTTCGGCCTCC | 9474 |
rs564128791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237285 | ATCCTTTAAAATTCA[A/G]ATCACACAATGCTCC | 9474 |
rs564147914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106309142 | GTTTTCCTCCTTTGC[A/G]GTAGACACTCTAGCC | 9474 |
rs564149799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235259 | GTAAAGCTACAAATC[A/G]TTCTTCAAATGGAAC | 9474 |
rs564212043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295207 | AACAGACCTTTTAAC[A/G]TCTTCAATTTATTTT | 9474 |
rs564220850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301262 | GCTCTAATCAGACAT[A/C]ACCTCCTTGTAAGCT | 9474 |
rs564258768 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243114 | TTTCTCTCCCCAAAC[C/T]GGTATCTAGATTCTT | 9474 |
rs564263468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244992 | AATCACCACCTGTTT[A/C]CAAGTGCTAAATAAC | 9474 |
rs564288903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234600 | GTACCTTAGCCTATC[A/G]TTGTTTGAATGGCTC | 9474 |
rs564332120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257911 | CTGTGTAGAGTGAAA[C/T]CTATCAAACCCCTTG | 9474 |
rs564379154 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106230742 | CTCTCAGATGCTAAG[-/A]AAAAAAAGACATATT | 9474 |
rs564404322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264164 | AATGACCTGATGGAG[C/G]TGAAAAACACAGCAC | 9474 |
rs564446422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236380 | CAGAAAGTAAGCATA[C/T]GTTGAATTTTGAAAG | 9474 |
rs564496348 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313325 | GTCACCTGTTCAGAG[C/T]GAAGGAAGAGGTCAG | 9474 |
rs564503059 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185974 | TCTCACTGTTCATTA[C/T]CAAAGTTACAAGATT | 9474 |
rs564510751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265447 | TACACAGATCAACGA[A/G]ACATAAAATTAACAA | 9474 |
rs564511301 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233298 | TAACAGGTTTCTGCC[A/C/G]AATATGGATTCCCAG | 9474 |
rs564511350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106226491 | AGATGCTGGACTTAC[C/T]GGACAAAGACTTTAA | 9474 |
rs564512012 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106287100 | TATAAAACAGCTACC[A/T]ACATTTATAGCTGGG | 9474 |
rs564547826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106286379 | TTCATATTTTTGGTC[C/T]TGTTTTCTAATTGTT | 9474 |
rs564554430 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202644 | AGGAAAGAAGTGCCA[C/T]GATATCCAAAACTTA | 9474 |
rs564642449 | in-del | -/G | 0.494774 | 0.0508504 | intron-variant | ATG5 | GRCh38.p7 | 6:106243526 | AGCAAGACCCTCTCT[-/G]GGGGAAAAAAAAAAA | 9474 |
rs564663088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106215784 | CATCAAAGTTAAAAA[C/G]TTTTGTTCTTCAAAT | 9474 |
rs564663727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222860 | TAAGGATTAAATAAA[C/T]ACATGTAAAATAATT | 9474 |
rs564721394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106254547 | TAGCAAACAAAGTGT[A/G]GCATAGTGGAAAAAG | 9474 |
rs564727438 | in-del | -/ACTTGACC | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106276503 | AGCTCAAAGCAGTTG[-/ACTTGACC]ACTTGACCTAAGGAC | 9474 |
rs564740871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106193669 | TAAACTTTGAAAACA[A/G]TATTATTTTATCTGC | 9474 |
rs564753971 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325744 | TCTGGTATCCAGCGA[A/G]TACAACCGGCAACGC | 9474 |
rs564769241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106322369 | AACTACCTAGAAATA[C/T]CAAATACTTACTAAA | 9474 |
rs564772856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106279219 | ATTTTCTAAACCACA[A/G]CAAGGAGAAAGGGAA | 9474 |
rs564777589 | in-del | -/CTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311829 | GTGCAATTTGATCTC[-/CTT]CTTTTTTTTTTTTTT | 9474 |
rs564797149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190092 | AAATATTCATTGTAG[C/T]CCATATTCAAATTTA | 9474 |
rs564802028 | in-del | -/TG | 0.167484 | 0.23599 | intron-variant | ATG5 | GRCh38.p7 | 6:106288934 | AACTACTGATCCAAA[-/TG]TGTGTGTGTGTGTGT | 9474 |
rs564807005 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210247 | CTCCATCCTGGCTGA[A/G]AAACCCAGAACAGTC | 9474 |
rs564809284 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237888 | GACATAAGCACAGTA[C/T]AGAGCCTTAGCTTCT | 9474 |
rs564840104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290536 | TGCCCAGGCTGGTCT[C/G]AAACTTCTGGGCTCA | 9474 |
rs564872937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275987 | ATTTACAAAAGCAGA[C/T]GGCTGGCCCATGATC | 9474 |
rs564886772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106325016 | AGGTTCCTCAAGTTC[A/C]GGATAATTTTAAAAT | 9474 |
rs564887528 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235825 | CTGCAAAAAAAAAAT[A/T]GCTTAATTGAAGAAT | 9474 |
rs564887828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106212223 | TACTAAATTTCTAAG[C/T]AGCATTAATTGAACT | 9474 |
rs564908118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106275060 | TAGCATAATGTCAGA[C/T]ATACACAAGGTGCTC | 9474 |
rs564937465 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106306031 | CTTACAGCATGACAT[-/A]ACTGTGGAAGTGATA | 9474 |
rs564948467 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195465 | GAAACAGTGACTCGA[C/T]GTTTTGGATACTCTA | 9474 |
rs564954032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262163 | CTTCAACCTCCGCCT[A/C]CCAGGTTCAAGTGAT | 9474 |
rs564976765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106310793 | TATTTAAGTGGAACC[A/G]TATAATATTTGTCCT | 9474 |
rs564982750 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211257 | AAATAACCAAAGGGG[C/T]GAAACTTAACAGATG | 9474 |
rs564983509 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289679 | CATTTAAAAAAAACA[A/T]TAATTCACTTAAAAA | 9474 |
rs564992860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268424 | AACACTTTTACACTG[C/T]TGGTGCGAGTGTAAA | 9474 |
rs564992923 | in-del | -/GCACTCCTTAACCACACCCAC | 0.193653 | 0.243567 | intron-variant | ATG5 | GRCh38.p7 | 6:106196821 | TTCTTCCCACTCTAG[-/GCACTCCTTAACCACACCCAC]AAACTAGAAATTGGC | 9474 |
rs565000291 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262229 | AGGCGTGTGCCATGC[A/C]TAATTTTTATATTTT | 9474 |
rs565001247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189352 | GCTCATGTCTGTAAT[C/T]CCAGCACTTTGGGAG | 9474 |
rs565029323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106220264 | CAATATGTAATATCA[A/G]TATAATCAATGCACA | 9474 |
rs565034236 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234802 | ACAACCTCTACTCAG[C/T]TCTACTACAAACTAT | 9474 |
rs565038897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310013 | TGCCTTGGCTTCACT[C/T]AAAATTGCTAAAGAA | 9474 |
rs565066815 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106187086 | TACATATTTTGAAAA[C/T]GTAAAATAGAAATGT | 9474 |
rs565094012 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274977 | CAGTTCTGCCTCCAC[C/T]TTTCTATAAAGCTCT | 9474 |
rs565117545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106305137 | CACATTAATTATATG[C/T]TTGGGATTATTTTTC | 9474 |
rs565125746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106312949 | AAGTCTAGCCATGGA[A/G]GAAAAGCCAAAGTTG | 9474 |
rs565163244 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106266898 | ATAGTCAATATCATA[C/T]GGAATGGGCAAAAGC | 9474 |
rs565200568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106273800 | CAACCCACCAGTCTA[C/T]ATCACACAAACCTCC | 9474 |
rs565206547 | in-del | -/AGT | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106195243 | GAATCACTTGTAGGG[-/AGT]AGAAGACAATGGTGC | 9474 |
rs565215698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303512 | ACAGCATTTTTACAC[A/G]ACCTTTTCCAGAAAA | 9474 |
rs565221418 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106204085 | CCTGTCGGGGAGTAG[G/T]GGGCTAGGGGAGGGA | 9474 |
rs565222457 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ATG5 | GRCh38.p7 | 6:106319438 | CAGGTGCTAGAAGAA[G/T]AATAATGGACTTTTA | 9474 |
rs565244794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106210033 | TGATTCATGTTTAAA[A/G]TTTGAGAAGCACTAG | 9474 |
rs565249854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304046 | ATTTCTATTTGCAGA[C/T]GTCAAGACTGTTTAC | 9474 |
rs565256935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106321699 | TTAATATCAGCTCCT[C/T]GGGAAGTTTTCCCCT | 9474 |
rs565265889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241522 | AACTGAAAACAGGGT[A/G]TACACCCATTTCAAC | 9474 |
rs565288014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296848 | GCAAGCAGACTCCAT[A/T]CTGGAATCAGTTTTT | 9474 |
rs565308048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106259857 | AGCAAAGAGTTGGAA[C/T]CCAAATGTCTATCAA | 9474 |
rs565314780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106246785 | TATACAAGTAAGATA[C/T]TTTGCTGGGCTGTGG | 9474 |
rs565342466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316812 | ATTTCATCCTCTCTA[C/T]AATTTAATCCCACCA | 9474 |
rs565346089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266259 | TAGAAGAAATGGATA[A/C]ATTATTGGACACATA | 9474 |
rs565349682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231280 | CTGATATGGAGAGAT[A/C]TAATGTTACTGCTAA | 9474 |
rs565351600 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218728 | CAGAATTGTCCCAAG[A/C]TGATTCTAAGTTACT | 9474 |
rs565400949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253103 | ATTAATTTCTTCATA[C/T]GTAATATGTTAAACA | 9474 |
rs565414212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224865 | CAGGCTGGGCAAAAA[A/G]AGCGAAACTCTTGTC | 9474 |
rs565456342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238509 | CTATTAACACACCAG[C/G]TCTCCTGAGCTAAGC | 9474 |
rs565492688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106246190 | TCCTTAGGCTCTTTG[C/T]TGCTTTCTGTTTAAG | 9474 |
rs565513552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225008 | TGACAAGCCATCATC[A/G]TTGCTGTTAAAATAA | 9474 |
rs565527905 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297779 | ACATATATATTTTAA[A/G]GTTCATTGGGGCTGG | 9474 |
rs565564043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106260782 | CAACAGAACTGCACT[A/G]ACTTTCTTGATTCAG | 9474 |
rs565586199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106296122 | TTAGGTTCTGAGTTT[C/T]TTTTTTGAGCAGTTC | 9474 |
rs565615712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281726 | CATAGAGTAAGTGTA[A/T]GTTCTAACTTTACTT | 9474 |
rs565629615 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254543 | GGAATAGCAAACAAA[C/G]TGTGGCATAGTGGAA | 9474 |
rs565638890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266484 | AAAGAGGGACTCCTC[A/C]CTAACTCATTTTATG | 9474 |
rs565678954 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231160 | AGCCAGAGTGCACGT[A/G]CCTTTTTCTCTCTCA | 9474 |
rs565725190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106253342 | GCAGTGCCAGTCCTG[A/G]AGGAAGTTCATCCTT | 9474 |
rs565734979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323158 | TAGCCAGGATGGTCT[C/T]GGTCTCCTGACCTCG | 9474 |
rs565743777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272673 | GAAGGGATCGTGCCT[A/G]TCATATTTACCCCAG | 9474 |
rs565773423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303685 | AAACTGAATCCAACA[A/G]TGTATAAAACTTATT | 9474 |
rs565782421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106280843 | CTAGGATTTAAGGCT[A/C]ATTTGACTCAAGTCC | 9474 |
rs565783467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187929 | AACAATTCCAAAGAT[A/G]ACCAAATAAAACATT | 9474 |
rs565796898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315579 | ACATATTAGCTCACA[C/T]ATAACATACAATAGC | 9474 |
rs565821208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203763 | TTTTTTTACTTTTTT[A/G]TAGAAGGGGGTCTCA | 9474 |
rs565825587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216077 | CACTAAGACTGCTGT[A/C]ATTAAAACTATAGAA | 9474 |
rs565832363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210820 | GTTATACAATTAATT[C/T]ATATAAAGTATTTAG | 9474 |
rs565879458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311259 | TATACAGCATACAGG[A/T]TAGACAGCAAAAAAG | 9474 |
rs565911386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236775 | TTTTTGTATAAGTTG[C/T]TTTACTCTGTGTATG | 9474 |
rs565945548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310310 | CTGCAATTTTCTGTT[C/T]CGTTTGGCCTGTGGG | 9474 |
rs565965704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302781 | ATTAAACACATTTCT[A/T]AAAAAAACTAAGATT | 9474 |
rs565985578 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106243903 | ATAAGTAGGAACCAT[A/C]CTTTTTTTTTTTTTT | 9474 |
rs566001276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307932 | AAGCCTAGTTAAGAT[A/G]TGTTTCTGGCACAGT | 9474 |
rs566003347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257526 | CATACATGCAGTCCA[A/C]TGTTGACTGAAACAT | 9474 |
rs566053824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251130 | ATCTCAATTTGCTTG[C/T]TCTGGAGGCCTGCAT | 9474 |
rs566090259 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106206150 | AGAGGTGAAGCCTTT[C/G]AGAGGTAATTAGGTC | 9474 |
rs566090974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106258198 | ACATAGGTAGATCCC[A/G]TCTCTAACAAAAAAA | 9474 |
rs566102991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300625 | CGTACCTAGGCTACA[C/T]GGTGTAGCCTAATGT | 9474 |
rs566146544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265042 | ATTAAAAGACACAGA[C/G]TGGCAAACTGGATAA | 9474 |
rs566179293 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199786 | CCAAGATTTAATGAT[C/G]GTAAATAATATGTTT | 9474 |
rs566183474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264343 | AGAAATATGGGACTA[C/T]GTGAAAAGACCAAAC | 9474 |
rs566183514 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106271864 | TACACTTTTAAAAGC[C/T]ATGCATAGGATTAGT | 9474 |
rs566184626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106195001 | ACGACAAAAACAATT[C/T]ACCTGAGCTCACCTT | 9474 |
rs566223021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202997 | ATGGTTGAGAGAGAG[A/G]CAGAGAGAGAGAGAA | 9474 |
rs566228623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106212439 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGGCCA | 9474 |
rs566284353 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235570 | ATCCACCTTTAAACA[A/C]TGGGCTTGCAACTTA | 9474 |
rs566304625 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318610 | CCATTGTTGCTTACA[C/T]GTATATTTTTTGCAA | 9474 |
rs566315089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234035 | CATTATTGGACAGGG[A/G]AAATGATTAATCCTA | 9474 |
rs566344751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194369 | TTTTGTCCAAATACT[C/T]AAAAGTATCTGCTTT | 9474 |
rs566347160 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231862 | AGGCCACCGCTTTAG[C/T]CATGGCCCTCAGGCA | 9474 |
rs566350444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294106 | ATGTTTTGGATTTTG[C/T]AGTCTTAGATTCTGG | 9474 |
rs566366682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287756 | TTTTAAAAATTCCAT[A/G]CACTGTTCTCAACAT | 9474 |
rs566387030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294776 | TGAGCCCGAGAGGCA[C/G]AGGCTGCAGTGAGCC | 9474 |
rs566414824 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200046 | GACAGTATTATTGTA[A/G]GTGCCCTTCCCCTTC | 9474 |
rs566480165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106282996 | AGGTCTCCCTATGTC[A/G]CCCAGGCTGGTCTTG | 9474 |
rs566480449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290796 | TACGCATTCCAAATG[C/T]TGACCCTTTCACTAT | 9474 |
rs566504394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106254983 | TATTTACAACCAAAT[A/G]CCCTCTATGTCCCTT | 9474 |
rs566508987 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320068 | TTACAAATGATAAAT[A/T]TGAGATGAGGATGTC | 9474 |
rs566569119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106189632 | GTAAAAACAAAAAAT[C/T]AATAATAAAACAGTA | 9474 |
rs566612624 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259406 | AATTTGAAATTATCC[A/T]CCCAGTGTTTCTCAA | 9474 |
rs566614285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290157 | TCAGCTTCCCAAGTA[G/T]CTGGGACTAGAGGTG | 9474 |
rs566637007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191436 | GAGGATCACTAACAC[A/G]TCTCCCAGTTCCAGT | 9474 |
rs566638577 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297548 | AAAAATTAATGAGCA[A/G]TTAGTTGCATTCAGG | 9474 |
rs566673590 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106198676 | CAGCTACTAGGGAGG[C/T]TGAGTCACGAGAATC | 9474 |
rs566676723 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268576 | AAAGACACATGCAAA[A/T]GTATGTTTACTGCAG | 9474 |
rs566712682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318624 | ATGTATATTTTTTGC[A/G]AGACCTCAAGGGAAG | 9474 |
rs566713381 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106249006 | ACCAAAGATTTTTTT[A/T]AAAAAGCTTTGAAAG | 9474 |
rs566735583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106298412 | TTAAATTAGCTGGGC[A/G]TGGTGGCATGCACCT | 9474 |
rs566758803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284604 | AAGTGATACAACTGC[C/T]TCATCCCCACAAAGT | 9474 |
rs566759658 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283115 | TGAGATTTGAATGTT[C/G]AATCAATTTTGTACT | 9474 |
rs566762458 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300527 | AACATGGATATGTTC[C/T]GAGAAATGCATTGTT | 9474 |
rs566804644 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106246535 | AGAATAAATTCAAAA[A/C]GGAAAACCTTTCCTC | 9474 |
rs566827151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296425 | AGTAAGAATTTGAAA[A/C]AATAACATGATGCCT | 9474 |
rs566831335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196905 | TCCATTAACAAAATA[A/C]ACAATATAAAATTTC | 9474 |
rs566848698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106239470 | ACACTATGGGGAACT[C/G]AATAAGTGATTTTAA | 9474 |
rs566876183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324442 | ATCTCCCACAGATGC[C/T]GAGGGACAGGAAAGA | 9474 |
rs566887488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238623 | TACGAACAGAAAAAG[C/G]TGAATAAAAGGCTGA | 9474 |
rs566973287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106196047 | CAAAGCACTTGAATG[C/T]TTTTCATTTACGTGT | 9474 |
rs566979569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106320604 | GTGGAATTAATATTA[C/T]CCAAGTCAAAAGGCT | 9474 |
rs566979792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318577 | TGAAAGATAAATTGG[C/T]ACTTTATTTCCCATA | 9474 |
rs566987131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106204304 | TTTCCTAATTCTATG[C/T]TTATGTATTCACTGA | 9474 |
rs566993569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267710 | AACCATCTGATCTTC[A/G]ACAAACCAGACAAAA | 9474 |
rs567011473 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209461 | ATGACTCCACTGATA[C/T]AACATTAGTGAAATG | 9474 |
rs567016047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219566 | GTGTATGAAATATTA[C/T]AAGTAATCTACAGAT | 9474 |
rs567017063 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325786 | GGCAGCGCACCACAA[A/G]TCCAGTCACCCTCGG | 9474 |
rs567047691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218948 | CTTTTTAGATTACTG[A/C]AGCAAAGAAAAGGAA | 9474 |
rs567047806 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286186 | CTGATACCCTGCCTA[C/G]CAAGTTCCAACCACT | 9474 |
rs567083571 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290801 | ATTCCAAATGTTGAC[C/T]CTTTCACTATGAAAC | 9474 |
rs567148869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106254162 | TTTCCTAATCTTTAC[A/G]TAACTGCTTCTCATC | 9474 |
rs567149009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248095 | CACTAGAGTGCTTCA[A/G]TTAAGATGTCTGAGG | 9474 |
rs567149121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106239671 | AGTCAAACTACTTTA[C/T]TATAAACCAGGGGTG | 9474 |
rs567159744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190333 | ACAGTGAACCCACTC[A/T]TGCAAATCCTTTTCA | 9474 |
rs567168285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106274623 | AAACTTCTTTTGGAA[A/G]AAAAAACTCTACATA | 9474 |
rs567169039 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257677 | TCTAATTCTTGTGAG[C/G]AATCACTCTAGGCCT | 9474 |
rs567183123 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106304574 | GTAAAATTCAGACAC[A/G]AAAGGCTACATACTA | 9474 |
rs567185012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261709 | GAGTATGGTGGTAAT[C/T]AGGGTGATAATGGTA | 9474 |
rs567200780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106226128 | CCCCAACATTCACAC[A/G]TAGGCCCCTGGCAAA | 9474 |
rs567228123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106231123 | TATGCCCCCTCCAAG[C/T]GGTGGGAGGAGAATT | 9474 |
rs567272408 | snp | A/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184037 | AGAATAAACACTCTT[A/T]ATGTGAACAATCATA | 9474 |
rs567291996 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263477 | CTGATCCTGACAAGA[C/T]GGATTCTCCCAGCAC | 9474 |
rs567329274 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216352 | TGGAGACAATCCACA[A/T]GTCTATCAATTGGTG | 9474 |
rs567340279 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186040 | TTCGTTAAGGAAAGA[C/T]GGGTTTACTGTAATT | 9474 |
rs567340774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267632 | GCATGGTACTGGTAC[A/C]AAAACAGATATATAG | 9474 |
rs567341586 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303397 | GAGTAGATCTATATA[A/T]ATCAAAGAAATTGAA | 9474 |
rs567373242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267352 | GAGGACACAAACAAA[C/T]GGAAAAACATTCCAT | 9474 |
rs567377490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106275140 | AAAGTGACAACTGAG[A/G]TGAGCATTAAAGCAT | 9474 |
rs567385065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226532 | TTAAATATGCGCAAA[G/T]AACTAAAAAAAAGTT | 9474 |
rs567392228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302668 | AACATCAACAAATTT[A/G]AAAGATCCAAAATTA | 9474 |
rs567406513 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237396 | CATCTTCTTGCAAAA[A/G]AGATATTTCTTTATA | 9474 |
rs567428948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106295673 | GGCTCAAGCGATCCT[C/T]CCACCTCAGCCTCCT | 9474 |
rs567449561 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275662 | CCAAGGCAGAAATAG[A/G]AAAAAAGTAATTTTA | 9474 |
rs567462647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205314 | AGTCCAACCTGAAAA[C/T]AACAAAGTCAAAGGA | 9474 |
rs567502295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324401 | GCATTTGAGGACTTT[C/G]GTATCCAAGGGAGGT | 9474 |
rs567522417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106305278 | TATAACTAACTTTAC[C/T]ATATGTACTATTTCT | 9474 |
rs567528377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206035 | TAAGTCAATCAGGAC[A/G]ACAAAAAAATACTCA | 9474 |
rs567539439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106297317 | TCTATTTATATAAAA[A/C]GAAGACTGAAGGAAT | 9474 |
rs567543488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197538 | TGGGGTGGGGGGGGC[A/G]GGGGTGGATCCCTCA | 9474 |
rs567545118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318087 | GTTGAAGTCACTATA[C/T]TGTCACTATTGATAT | 9474 |
rs567558078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106291071 | GTCAATCATTCTTTC[A/G]AGTAAAATAATGGTG | 9474 |
rs567582711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189448 | TACAAAAAATAAAAA[A/G]ACTCAACCAAACAAA | 9474 |
rs567613239 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219090 | ATTATTTCTTTCAAA[C/T]TTTAAACGAGCAGAA | 9474 |
rs567617493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252679 | GTCTAAAATCCCCCA[C/T]GGGAGACATGGAGGA | 9474 |
rs567619414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188875 | TTTGTCACTGCCTAC[A/T]TATGTCCAAATATCT | 9474 |
rs567636585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237785 | TAATCACTGCTTATA[C/T]AGTTGGTTAGGATTT | 9474 |
rs567644633 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312740 | CCACAAGATGGGAGA[A/G]GCAACCAACAACATC | 9474 |
rs567671023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210131 | TCAATAACAGTTGCT[C/T]GGTTGGACAGTGACT | 9474 |
rs567674658 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300282 | AATCTCCTGCATAAA[C/T]GGGTTAAGTTCCAGA | 9474 |
rs567685696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245501 | TGTTCACTGAGGCAA[A/G]TGACTTAAAATTCCC | 9474 |
rs567693420 | in-del | -/AATT | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106210812 | TTGTGAAGGTTATAC[-/AATT]AATTCATATAAAGTA | 9474 |
rs567759841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106192983 | GAGGTAATAGTCAGC[A/G]AGGTCAGGTCAAAGA | 9474 |
rs567761283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232248 | TTTTCCTGTCCCAGA[A/C]AACGGTCCTCCAGAG | 9474 |
rs567762441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203163 | TCCAAAACAGCAGAT[C/G]CAGCCATTTCATCTG | 9474 |
rs567771405 | in-del | -/CTCCCTCCACAC | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106269784 | TTCCCGCTCGCGCCT[-/CTCCCTCCACAC]CTCCCTGCATGCTGA | 9474 |
rs567843167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106282893 | TGGGGCCCAAGCGAT[C/T]CTCCCAATTCAGCCT | 9474 |
rs567882851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290103 | AGTGGTACAGCTCAA[C/T]GTAACCTCAAACTCC | 9474 |
rs567898578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321967 | AGAAATTTTCTCCCT[A/C]AACTCCTCTCCAAAT | 9474 |
rs567900431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274513 | AAGTGCAGTTCTAAA[G/T]GAAATAAATGTGCCA | 9474 |
rs567980115 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327295 | ATATAATGGTAGAAT[A/G]TAATGGTAAAATATA | 9474 |
rs567980331 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186147 | TAAACCAATGTTTCC[A/G]CTTTCATGAGCTAAA | 9474 |
rs567986982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106191236 | GAATCTTATGATCAT[A/G]CCAGTGTAGAATTTT | 9474 |
rs567989007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231515 | TAACTTGCGTGCTAG[A/T]AGGACTAAGGAAAAC | 9474 |
rs568017463 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185570 | CTGCCAGGGACCACA[C/G]TGAAAAATTAGACCT | 9474 |
rs568050134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234870 | CTCCCTGGTCACCTT[A/G]CAAGATCAACTTAAC | 9474 |
rs568098687 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106249444 | TTCATTTGCTTTTAC[A/G]GCTGAATAATATTCC | 9474 |
rs568128998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200244 | ACCAAACCCACTGTT[A/C]CTAATTCTACTACTT | 9474 |
rs568130010 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106290083 | GATAGAGTGCAATCA[C/T]TGTGAGTGGTACAGC | 9474 |
rs568134197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248458 | CTCTCCCTAGATATT[C/T]GCACAGCCATTTTTT | 9474 |
rs568158867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268867 | GAACATCACACACAC[C/G]GGGGCCTGTCGGTGG | 9474 |
rs568165760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207612 | AGCCAGTAGAGCCAA[C/T]AGGTTAACCAATATT | 9474 |
rs568165826 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312838 | TTAGTGACTTTGGCA[A/G]GAACAGTTTTCTTGG | 9474 |
rs568233115 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222165 | TGCGTGAGCCACTGC[A/G]TCTGGCCTAAAGTGT | 9474 |
rs568271673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106194798 | CGCCTAGCTTACCAC[A/G]TTGTTATACATTACA | 9474 |
rs568304427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271348 | GCATTTGGGAGCTGA[A/T]TAGGTCATAAGGGCG | 9474 |
rs568311920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229080 | AACCACGACTTTCTT[C/G]AAAGTGTAGCCCCAA | 9474 |
rs568336813 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252310 | ATCAAATCAAAAGCA[A/T]AAAACTGAAGGACTG | 9474 |
rs568343006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263502 | CAGCACAGAACACCA[A/G]CTCTGCTAAGGGACC | 9474 |
rs568351180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106298657 | ATGAACCAGAAAAAC[A/G]AAGGAGTAAGATAAC | 9474 |
rs568359776 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106286797 | CAATGCAGCTTATTA[A/C]TGACAGCCAACAAGA | 9474 |
rs568362501 | snp | A/C | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106227587 | GGAGACCCTGTCTCT[A/C]TAAAGAAAAAATGTC | 9474 |
rs568418180 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106269395 | GCCTGCCAGTCCCGC[A/G]CCGTGCCCCGCACTC | 9474 |
rs568429766 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106220616 | GCAAATAGTTATTTT[A/C]AAAGTATGAGTAATT | 9474 |
rs568450324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319565 | CTTACCCTAAAGCAG[C/G]CTTCTTTACCTTATC | 9474 |
rs568466929 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATG5 | GRCh38.p7 | 6:106322945 | TTTATTTTGAGACGG[A/G]GTCTCGCTCTGTCGC | 9474 |
rs568473334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106199516 | ATAGGCAAATTATAG[A/G]GACAGAAAACAGACC | 9474 |
rs568477732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284441 | GAATCACTGCTCCTC[A/C]CAGGCTCAAGAGATC | 9474 |
rs568482960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106277120 | TGCATGCCTTACTTG[C/T]TCTTGATACCACAGA | 9474 |
rs568491046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106320143 | AAATTAGAAGCCACA[G/T]CCTAACTCAGGTTTC | 9474 |
rs568548900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249164 | AAATTCACCCCTTTT[A/G]AAGTATACAACTTAG | 9474 |
rs568558889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306379 | ACTTTACAAGCTAAA[C/T]TGAGGTTTCCCAAAT | 9474 |
rs568565261 | in-del | -/AC | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106196703 | ACTCCAGCCTGAGCA[-/AC]AGAGTGAGAATCAGT | 9474 |
rs568580134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106306249 | CAAGGAGAAATGGGT[C/G]CAAACACTATTTACC | 9474 |
rs568589075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255973 | TTATTTCTCTTGGCC[A/G]AAATTAGTTTATTAC | 9474 |
rs568616167 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325940 | CGCGACCAAACCTCT[C/T]CAAGTTCATAGCTTC | 9474 |
rs568620284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106213841 | GAGATATATGAAATA[C/T]CTAATGTAACAAGTG | 9474 |
rs568623169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106313299 | CTTTTCTTCATGAAA[A/G]AGGAAGTGAGGTCAC | 9474 |
rs568639080 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106313974 | GCCAGTCACCCAACA[C/G]TCTTCAAAAACACAA | 9474 |
rs568679994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228982 | TAGCCGGTTGAGATC[A/G]TGTCGCAGCCAGAAG | 9474 |
rs568709065 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215292 | TAAGTGTCTAACCCA[C/G]GGAAAAGTGATTCTA | 9474 |
rs568717397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292275 | GAATGAATTACTGTT[C/G]GTAATCAATTAATAT | 9474 |
rs568733429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312486 | TGGGAATTGTCAAGA[A/T]ATAAATGCTTGACAA | 9474 |
rs568760088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213395 | TTCTAAGAGTTGGAA[G/T]CTATATCAGTAGGTA | 9474 |
rs568795296 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106221450 | CAGCACTTTGGGAGG[C/G]CAAGATGGGCGGATC | 9474 |
rs568796489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106192967 | TTTTGTCTCAGCCAC[A/G]GAGGTAATAGTCAGC | 9474 |
rs568851867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106249379 | CATCTGGGTTTTTCG[C/T]TTGGCATAATATTTT | 9474 |
rs568873913 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320758 | CTAGACCATGAAACA[C/T]ACCAAACAGAAGACT | 9474 |
rs568892951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106249094 | GCTCTTTTTAAAAAC[G/T]TTTCAATTTCAAATT | 9474 |
rs568921722 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106284709 | GTGAAGGGGTAACTC[A/G]TTGTGTGGGGTTTTT | 9474 |
rs568929896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255808 | GACAATCTTTAAAGC[A/G]GCTTGTCAAAAAGAG | 9474 |
rs568931543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106206916 | AGGAATGCTGTAAAC[A/G]TTGATTTAGTATATA | 9474 |
rs568932724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106271631 | TCAAAATAGTATAAA[C/T]GAAGCTTTGTGTACT | 9474 |
rs568941618 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106263641 | GTGCCCCTCTGGGAC[A/G]AAGCTTCCAGAGGAA | 9474 |
rs568955431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275503 | AATAGCTACAAAAAT[A/G]ATTTATAACCAAAAA | 9474 |
rs568966443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213206 | CAGGGTATCACTATG[C/T]TAATGGATACAAAGA | 9474 |
rs568968623 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106219895 | TCCAAATGTGTATCC[-/A]ATCTTGTTTAATTAT | 9474 |
rs568980944 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106321461 | TCTCCCGGGTTCACG[C/G]CATTCTCCTGCCTCA | 9474 |
rs569037986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234830 | TATCTCAAGAACTCA[A/G]TGGTGACATGGAATG | 9474 |
rs569042479 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235410 | TACTATGCCCCAATT[A/C]CGCAGGAAGCAGTTA | 9474 |
rs569045148 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242275 | GTGAGCCACCACACC[C/G]AGCCAAAAAAAGGAC | 9474 |
rs569080858 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185325 | TGTAAGCCTTTTAGC[A/G]TACTCAAATGGGTCA | 9474 |
rs569082404 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244728 | GGTCACACATAATAT[C/T]GATCATCAGTTGTAT | 9474 |
rs569117060 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106278282 | AACTTAAGAACTATA[C/G]TTTGAAGAGTGCTTG | 9474 |
rs569159936 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306640 | GCCCCGCTAGTCACA[C/T]AAAATTCTGAGATAA | 9474 |
rs569164891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106233040 | GCACTCTTGTCCTTT[G/T]GTATGTGGATGATTT | 9474 |
rs569178073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242025 | ATAGCCAAAAGGTGG[A/C]AGCAACTCCAGCAGA | 9474 |
rs569218017 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106233655 | AGCAGTTAAAATAAT[A/G]CAAGGAAGAGATCTG | 9474 |
rs569219849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106276261 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 9474 |
rs569236221 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289812 | CACTAATTTGTATTT[C/T]TGCAAATAACTTTAA | 9474 |
rs569239004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190404 | CTTAAACACCCCCCA[A/G]AAAGCCTCACCTCCC | 9474 |
rs569255582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106318792 | ATTTATAGGATCTTA[A/T]AATGTTAATCTTTCA | 9474 |
rs569288820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325910 | CATGCGCCAACGGGG[C/T]AGTACGCTTGAACTC | 9474 |
rs569357620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272035 | GAGGACTTCCCTGAC[C/T]ATCCTATTTAAAATA | 9474 |
rs569382239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262364 | CCACTGCACCCGGCC[A/G]GTCTAGGGTATATTT | 9474 |
rs569394840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106279888 | ATTAACCTCTTAAAA[A/G]AGAACTATATCCCCC | 9474 |
rs569397517 | in-del | -/ACAGCATAAA | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106306319 | TAACCACCATGAGGG[-/ACAGCATAAA]ACAGCAGCTGAAAGA | 9474 |
rs569398545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197429 | CTAATTGATAAAATC[A/T]TTTGTTATAGTGTGG | 9474 |
rs569424858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106319943 | AGATTAGATAATAAA[A/C]ATTAGTTAACAGTAG | 9474 |
rs569445553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106221385 | TTTAACCTAAACTTT[C/T]ATCAAATGTCAAAAC | 9474 |
rs569468177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255060 | CACCCTGTGGGCACA[A/C]TTTAGTTGCCATTTA | 9474 |
rs569471430 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106269317 | GAGCTAGACATAAAG[G/T]TTCTCCACGTCCCCA | 9474 |
rs569483183 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275341 | ATAAACAGAAAATAA[A/T]GTACCAAGGACTCCA | 9474 |
rs569492841 | in-del | -/TT | 0.000798881 | 0.01997 | intron-variant | ATG5 | GRCh38.p7 | 6:106205333 | AAAGTCAAAGGAATC[-/TT]TTCAAGAATTTGGAG | 9474 |
rs569511395 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260578 | TACCCCTCTTTTTCA[C/T]AAGTTGCTTATTTTT | 9474 |
rs569549169 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106301821 | AAGGATACTTAACCC[A/G]TATTAACTCACTTAA | 9474 |
rs569560968 | in-del | -/TAC | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317605 | GTGCTCTTTCCAGCA[-/TAC]TACTAGTGTTTTAAC | 9474 |
rs569595206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280589 | TGATCATTGGACATA[C/T]AGGGAGTTAGGTAAA | 9474 |
rs569599333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187759 | CTGATGATGTATGGT[G/T]ATAATGACTTGGCTG | 9474 |
rs569613399 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229338 | ACCACCCTTGCCAGG[A/G]CCCCAAGTTTGTAAA | 9474 |
rs569616110 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106227522 | GATCGCTTGAGCCCA[A/G]GAGTTGGAGGCTGCA | 9474 |
rs569623530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272595 | TCCAGTTATAAATGT[A/G]ACAATTACGTAAAAG | 9474 |
rs569633942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288144 | CCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 9474 |
rs569690885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302460 | CAGAAAGAAAAATTA[C/T]GGCACTGGGGAAGAT | 9474 |
rs569781394 | in-del | -/A | 0.192401 | 0.243274 | intron-variant | ATG5 | GRCh38.p7 | 6:106266034 | ACATGAAAAACCCTC[-/A]AAAAAAAAAAAATCA | 9474 |
rs569781569 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262958 | TGCAGGAGTCTTTTT[C/T]GTACTTCAGTGGCGC | 9474 |
rs569790675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194344 | ATCACGAGATACTAA[A/C]AAGCTTCAATTTTGT | 9474 |
rs569836277 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309808 | AAAATATGTAAGTAT[A/C]ATCTATTAGTCTAAT | 9474 |
rs569844246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106229524 | GCAGAGAGACAAACA[A/G]GGAGTCAGAGAAAGA | 9474 |
rs569890100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316421 | GTATAAATTCAAAGA[A/C]AAGAGTACAACAAAT | 9474 |
rs569936399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251114 | GCTTGCCCTTATCAA[C/T]ATCTCAATTTGCTTG | 9474 |
rs569938486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106243270 | CAATGGGAAAGGAAG[C/T]AGAATTCTGAGGATT | 9474 |
rs569959940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216990 | TTATCATATGGGTGG[C/G]AGGGGAAATCATTCT | 9474 |
rs569976291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250272 | TTTAAAAAATTTCTT[A/C]TTACACCCCTGTCCT | 9474 |
rs569987676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214979 | ATCATACCAAGGGAA[A/G]TATAGTTTAAATTTC | 9474 |
rs569994821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224490 | AAGAGGAAACTGGAC[A/G]CTGAAACAGAAGAAG | 9474 |
rs570025237 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106263786 | CAAAAAGAAAATACA[A/T]CATCAACATCAACAT | 9474 |
rs570029537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314860 | TTCTAGACAGAAAAC[A/G]GTTGATATTTCCAAA | 9474 |
rs570094941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321825 | TGAACTGGGAGTTCT[C/T]TGACAGCAAAATTTA | 9474 |
rs570188019 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272676 | GGGATCGTGCCTGTC[A/G]TATTTACCCCAGCGT | 9474 |
rs570201512 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261090 | AACAGAGACTAGGCA[A/C]GTTTAAATTAGAGTT | 9474 |
rs570210241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258007 | AACAAGTACACAAGA[G/T]ATTGTTCCTTTCACT | 9474 |
rs570220334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308557 | AAAAATACTAAGTAG[G/T]TTTTTGAATTTTAAG | 9474 |
rs570223453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202258 | AAATGTTTAACATGA[C/T]AAATTCAGGTAAATC | 9474 |
rs570250769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208775 | TGCAAACCATATTTC[C/T]GAGAAAGGTCTTGTG | 9474 |
rs570259217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293555 | TTCTGTGGTTATTAC[C/T]ATTAACATTATAGCA | 9474 |
rs570273129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294050 | GAAAATCTGAAATGC[C/T]GGAATGAGCACTTCC | 9474 |
rs570274599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234097 | TCGGACTTACTTCAC[A/C]CATACTGGTATGTCT | 9474 |
rs570307395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106315604 | AATAGCTCAGTGAAC[C/G]TATCGTGTGTGTGTA | 9474 |
rs570342125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308703 | ACTTTAAGCACAGCT[C/T]ACCACATAAATGCCC | 9474 |
rs570342165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201370 | TTTCTGCATTTTCTT[C/G]GTGTTCTTTATGTTG | 9474 |
rs570345901 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197294 | TGTGAAGCTAAAGTG[A/G]GAGTATCACTTGAGT | 9474 |
rs570366087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322086 | CCAATTTCAAGGAAC[C/T]GTCTTGGAAATAAAG | 9474 |
rs570440729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106235804 | TCACTCTATTAAATA[C/T]TGCAACTGCAAAAAA | 9474 |
rs570446495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106229661 | TATAACACTCCAATA[C/T]TACCTTGTTGTCAGC | 9474 |
rs570472577 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186239 | AGTGGCACATACTTC[C/T]ATTTTCTTCTTAGGC | 9474 |
rs570475520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106193042 | AGAAATACATCAAAC[A/G]CTGATTTTAAAAGGG | 9474 |
rs570481071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243146 | AATATTTTTAGCACA[C/T]AGAAGTTAAATAGAT | 9474 |
rs570503514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293474 | ATGTTTTTTACTTTT[A/T]GAACTTAAAATTTTA | 9474 |
rs570522809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228885 | ACCTTGGTCTGCCTG[G/T]AGCCAGCTTCCACTT | 9474 |
rs570525594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224370 | GCAAATGGCAAGAAG[A/G]GAATAAATGAAGACA | 9474 |
rs570553221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263033 | TGCTGAAGCCACAGA[C/G]TCAAGTGGTCTCGCT | 9474 |
rs570569186 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251526 | AAAGGAAGACACGAT[-/A]AAAAAAAAATCTGTA | 9474 |
rs570581484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201227 | GGATATGAAGGGCCA[A/G]TGTGTATGTATTATA | 9474 |
rs570656360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106258238 | CCAAGCATTGGTGGT[A/G]TATGCCAGTAGTACC | 9474 |
rs570661179 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ATG5 | GRCh38.p7 | 6:106265221 | GTCCCTGATAAAACA[A/G]ACTTTAAACCAACAA | 9474 |
rs570662896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106186935 | TCTTAATTACTGTGC[C/T]TACTTAAGATTGACG | 9474 |
rs570700621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223377 | GGAAAAACATATCTG[C/T]CAAATAAGCTTATAA | 9474 |
rs570731303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106213477 | GAATTTCAAAAGAAG[A/G]TAAAAATAATGGAGG | 9474 |
rs570740382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106257329 | AACATAGTCGTTTAT[C/T]ATTATCAATTACTGT | 9474 |
rs570773931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209897 | AGAGCTTTGTTAATC[A/C]AAGTTTTCTCTGAGG | 9474 |
rs570787442 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306873 | AAAGAAATGGGAAGC[A/G]TTGCCTTATCTATGC | 9474 |
rs570806489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230238 | CTTAACGTACTTACC[A/G]AATCAAAAAGACTAT | 9474 |
rs570806989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320307 | TTGGAGATATTAATA[A/C]ATCCTATAGTGTTCA | 9474 |
rs570813623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263640 | GGTGCCCCTCTGGGA[C/T]GAAGCTTCCAGAGGA | 9474 |
rs570818138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321046 | AGGGCAGGGAAGATT[C/T]AGATGCTGACAGCAT | 9474 |
rs570864781 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106270115 | TATTCACTTAAATCA[A/T]GTAATTTCAGGAGCA | 9474 |
rs570870406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106277218 | GTAATAGCATAGTCC[A/G]AAAGTTAAAACTAGA | 9474 |
rs570963341 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184219 | ATTATAAAGGACAAT[A/G]ACTTACTTTAATCTG | 9474 |
rs570996928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292943 | GGAAAAGCAATAAAT[A/T]ACTTCACTTAAAAAG | 9474 |
rs571014317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106200415 | AATGCATTACCTGTT[C/T]CCTTCATGGATTTAA | 9474 |
rs571014562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208143 | TTTATTATGGAACCA[C/T]GGACACAACTACCTA | 9474 |
rs571022466 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255394 | GGAGTCAGTAAAAAC[C/T]AGCTACCTCATGAAA | 9474 |
rs571028090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229763 | CATCCAGTGACCTGC[A/G]GATGGCCCAAATGCA | 9474 |
rs571054131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225100 | AATTTAATTTATTAT[A/G]TGCCAGGCACAATAG | 9474 |
rs571058949 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258109 | TTTGCACTTGTAATG[A/C]TTGATGGCTCAAGTC | 9474 |
rs571085480 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251901 | GCTGGAGTGCAGTGG[C/T]GAGATCTCTGCTCAC | 9474 |
rs571122548 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106306939 | GGAGTCTGATACATG[A/T]TCATGAAGCTCAGTA | 9474 |
rs571126069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218755 | TACTTTAAACATGTA[C/T]GCAGAGTCAGAATAT | 9474 |
rs571148686 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317977 | AGTCAACAGCTGCAA[A/C]TGAGATTCACCTTTT | 9474 |
rs571155963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106207661 | ACAAGAAATGATGAT[C/T]TACTATAAGCTGAAA | 9474 |
rs571161892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106307737 | GATGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 9474 |
rs571168641 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273535 | GGCATTACCACCTTC[A/G]TATTTGTAATAAAAC | 9474 |
rs571190641 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106267260 | TGCTACAAAGACAAT[C/G/T]AAATACCTAGGAATC | 9474 |
rs571230230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106218005 | ATGATTATTAAACAG[A/G]GTTCTAAGAAAATAG | 9474 |
rs571281883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262926 | TGGGCAGCCATTTGG[A/G]CAGACACCGAGCTAG | 9474 |
rs571283794 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206354 | CTTGATCTCTGACTT[C/T]CCAGCCTCCAGAACT | 9474 |
rs571294702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311430 | CAAAAGACAAATAGG[A/G]GTGAAATGAACATGG | 9474 |
rs571295355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106266620 | AAATTCTGGCAAACC[A/G]AATCCAGCAGCACAT | 9474 |
rs571305971 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314864 | AGACAGAAAACGGTT[G/T]ATATTTCCAAAGTTA | 9474 |
rs571317606 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106237232 | AAAAGCAAAACTAAA[A/C]CCAATAAGAGGAAAG | 9474 |
rs571332493 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106273521 | TTTGAGTCTTATGAG[G/T]CATTACCACCTTCGT | 9474 |
rs571356316 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306300 | GCCATATTGAATACA[A/G]GAATAACCACCATGA | 9474 |
rs571375074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106282612 | ATTCGATAAACCATC[A/G]TGTAGCATGACTTTA | 9474 |
rs571378628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106290325 | ATTCATTCTTTCATT[C/T]GTTCATTTATTTTTA | 9474 |
rs571399878 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288367 | CTCACCAAGTTTAGG[A/C]ATCAAAATGTCCTTA | 9474 |
rs571408160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209548 | TGCAGTAAGGTAGGT[A/G]GCTGTGGCTATAAAA | 9474 |
rs571428494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106205263 | AGCAGGACTGTACCC[A/T]CAACTCAAAGAAAAA | 9474 |
rs571430087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106196971 | TTAACTTTAGTTTTT[A/G]CAGATAAAACACAAA | 9474 |
rs571435590 | in-del | -/CT | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106210900 | TTAAATGTGACTTGA[-/CT]CTCAACAGAACTCTA | 9474 |
rs571469948 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204325 | TATTCACTGAATACA[C/T]AGTATTTTAAAATAG | 9474 |
rs571483112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106210943 | TATGTATTCTGTATT[A/G]AGCTGTCAAAAAAAA | 9474 |
rs571490244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231381 | TCTCAGTCAGGTCAA[G/T]GATAGGTCGACAACA | 9474 |
rs571513025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211569 | AAAAAAATTAGCCGG[A/G]AGTGGTGGCGTGCAT | 9474 |
rs571532945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106303726 | ACCAAATAAGATTTA[C/T]TAAATGTATACAAGG | 9474 |
rs571569020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304409 | CTTTTCTCAATATAG[C/T]CCCAGAATGGAAACA | 9474 |
rs571569969 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106307029 | CCATCTCAAAGGATT[-/AG]AGACGGGACCCAAAA | 9474 |
rs571597142 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239572 | ACAGATATCAGAACG[C/T]TAAAATTAAATAAAA | 9474 |
rs571607870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244702 | CACCTTTAGACTATA[A/G]CCTTCTAAGGGGTCA | 9474 |
rs571626546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203655 | CTCTGTCACCCAGGT[G/T]GAATTGCAGTGGTGC | 9474 |
rs571635609 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228596 | TCTTAGAAGCAGCCC[C/G]CCACCATCTTCGGAG | 9474 |
rs571654770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106294875 | AAGAATTTAGGATGA[A/T]CGCCCGGTCGGTAAA | 9474 |
rs571659866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252615 | TCCACTTAAGCTTTA[C/T]GAGAGGTAAAAACTC | 9474 |
rs571682511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216898 | CTCTAAATAAATAAA[C/T]AAATAAATAAATAAA | 9474 |
rs571698359 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATG5 | GRCh38.p7 | 6:106251997 | AGGCATGCATCATCA[C/T]GCCCGGCTAATTTTT | 9474 |
rs571701623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291281 | TACTACTACATCCAG[A/G]AAAGTCTTAAACTGG | 9474 |
rs571708457 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247077 | GACAATTTGCTTTCC[C/T]CTCTGAACACATAGT | 9474 |
rs571728588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251171 | TCTGTGGTTTCCCAC[C/T]CAGCTGCCACTCCCT | 9474 |
rs571765164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237727 | CGAATTCCATAAAAT[A/G]TATGATATGAACATT | 9474 |
rs571796764 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197437 | TAAAATCATTTGTTA[C/T]AGTGTGGTTGCTTGT | 9474 |
rs571825764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323595 | CGTCCTTGACCCTTC[C/T]TCTACCTGACTGCTC | 9474 |
rs571826202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106295643 | GTCAGAGCTCACTAC[A/C]ATCTTGACCTCCTGG | 9474 |
rs571834322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289233 | GATTTTCTGCCTGAA[A/G]ATTAACACTTACCCA | 9474 |
rs571844294 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212393 | TGCCTGTAATTCCAG[A/C]ACTTTGGGAGGCCAA | 9474 |
rs571866133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106236845 | CAAACACAGTGCTTA[C/T]TTCACTAATGAGTAT | 9474 |
rs571916471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281890 | GTAATGTAATGTCTC[C/T]TTGTGGTTTTAATTT | 9474 |
rs571973820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106294417 | TTATATATATAAACA[C/T]AGATATATGTTTATA | 9474 |
rs571992104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106288399 | AAACCAATGAGAAAA[A/G]CTTGAAGAAGGTACC | 9474 |
rs572007940 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294893 | CCCGGTCGGTAAAAA[C/T]AAAGCAGTGGGGGTA | 9474 |
rs572031987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301200 | GAGTTAGGCCAGCAC[A/T]TTCCATTTCCCATGT | 9474 |
rs572044858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106209276 | AAAGCAATCCCAGGG[C/T]TACCCATTAAAACAG | 9474 |
rs572060632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272122 | GCACTCATCATCATA[A/G]GACACATAATACATA | 9474 |
rs572097973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106243396 | ATTAGCCAGGCATGG[A/C]ACATGCCTGTAGTCC | 9474 |
rs572106146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235101 | GGAGCTTCAAAAACA[C/T]CAGACCCTGGGGCCT | 9474 |
rs572134718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242390 | ATGATTCCTCTTGTA[C/T]GAGGTACCTATGGAT | 9474 |
rs572176808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244967 | AATCTTTTTGACAAA[C/T]GCCTTCATTAATCAC | 9474 |
rs572242616 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325836 | GAGACCCCACGTGGT[C/T]CGAACTCCGCCCTCC | 9474 |
rs572271191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244282 | TAGAACAAAGTAGAT[C/G]ACTGAATGATCTTTG | 9474 |
rs572295362 | in-del | -/C | 0.0103295 | 0.0711199 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325558 | CTCCTCCTTCCGGCT[-/C]CCCGCACTGGTGGGG | 9474 |
rs572303621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201473 | TTACAAAATTAGCGC[C/T]ATGAAACAGGTCAAG | 9474 |
rs572310443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106251406 | AAGGTAAAATATATA[A/G]TTTTCTTATATTTTA | 9474 |
rs572338880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202875 | ACCATGTTGCCCAGG[A/C]TGGTCTCAAACTCCT | 9474 |
rs572374218 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106250354 | TGTGAAGGAAGACTC[A/G]CAGTATATTAGAAAT | 9474 |
rs572410012 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232662 | AAGGCCTAGTAAAAG[C/T]ATGCAATAGCCCCTA | 9474 |
rs572425565 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106193238 | TAAAAATACTTACAT[G/T]AACTTCTTCCGGATG | 9474 |
rs572435240 | in-del | -/TTCTTACATTCTTACATC | 0.00676609 | 0.0577691 | intron-variant | ATG5 | GRCh38.p7 | 6:106259609 | TTCCCTTCATCACCT[-/TTCTTACATTCTTACATC]TGTCTCTTCTGCTCC | 9474 |
rs572465405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299477 | ATTTTCTGTGTAAAT[A/G]AGAGGACCCAACTAG | 9474 |
rs572465779 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303570 | CAGTTTATAAAGCCC[A/G]TATAACCCTAATGCT | 9474 |
rs572467620 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106249643 | TCATTAGGTAACTCT[A/G]TTTAACTGATACATG | 9474 |
rs572470440 | snp | A/G | 1.68281e-05 | 0.00290065 | intron-variant | ATG5 | GRCh38.p7 | 6:106293130 | GAAACAGTATATTTT[A/G]AGAAAATAAATATTT | 9474 |
rs572472069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106204842 | CAGATATTTCTTTAA[A/G]GCAGAGTGAAAACAG | 9474 |
rs572499537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280006 | TGGCCCATTTTGTAC[C/T]TTTCCCAAATAATTC | 9474 |
rs572500611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106232794 | TACCTAACCCTTATA[C/T]TCTGCTTTCCCAAAT | 9474 |
rs572508752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106293590 | CATTTCCAGTCTTCT[A/G]CCTACACATACATAT | 9474 |
rs572535582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106239190 | TTTGTAAAAACACAA[C/T]AGGATGAGATTTTTG | 9474 |
rs572553477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271545 | TGAAAATAATCAGAC[A/G]TCTTCCCTAATCACC | 9474 |
rs572587600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106223479 | CTCAGCGTAGTAGAT[A/G]GCTTAGGGCAATCAA | 9474 |
rs572622956 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106229834 | TAGAAAAGTAACTTT[C/T]AGAGGAAACCTCATT | 9474 |
rs572657254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322324 | AAAACTAACCTACTA[C/T]CTGAAGTAATTTTCA | 9474 |
rs572668008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193981 | CAGTCAGGTTAATTC[A/G]TTTAACTTCTTGAGA | 9474 |
rs572691946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106315286 | CTTCTACTTTTCCAC[A/G]TCATCTCCAGGTAAA | 9474 |
rs572708523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189993 | TTACAGTGTACCATT[A/T]CTAATATAAGATATT | 9474 |
rs572740791 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106208830 | AATTCAACAGTTTTT[A/T]AAAAAAGCAAATAAT | 9474 |
rs572757813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106197814 | TATAAATTACCCAAC[A/C]TCAGGTGTTTCTTTA | 9474 |
rs572764642 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207172 | GTCATTTCTTAACAC[C/T]AAATGAAATGAAAAA | 9474 |
rs572795213 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185911 | AAAAGTGACAAAACT[A/G]TATGTTATTAAATGA | 9474 |
rs572824614 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106235677 | AGCCAATCATCTATC[A/G]CCTGAGAGCACAGCG | 9474 |
rs572855881 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106253529 | TTACCCTACAAAGTA[A/G]GTGCCACAGTCTTAG | 9474 |
rs572914301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317611 | TTTCCAGCATACTAC[G/T]AGTGTTTTAACTTTT | 9474 |
rs572914891 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210671 | AGCTTATGGTTCCAA[A/T]CCCAGCTCTGTCAAT | 9474 |
rs572968103 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325967 | CTTCTACCCTCTTCT[G/T]AGAATCTTGCGTCAA | 9474 |
rs572975010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106226945 | AAGGAAGGAAGGAAA[A/G]GAGGCTCAGAGACCC | 9474 |
rs572981391 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106188962 | AACAGAGGGATTCTT[A/T]GAATAGGGCAGCAGA | 9474 |
rs573025818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289442 | CTTTCCTCTAACAGG[C/T]CAGGATAAGAATAAG | 9474 |
rs573030536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235636 | CACTAAAATGCTAAT[C/T]AGACAAAAACAGGAG | 9474 |
rs573074957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211365 | GGGGGAGTCTCCTAC[A/G]GACACAGCAGGCAGA | 9474 |
rs573089043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106311748 | TGTGATTTGAAAAGA[C/T]CACTCCAACTGCAGA | 9474 |
rs573092697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106312480 | AAATATTGGGAATTG[C/T]CAAGATATAAATGCT | 9474 |
rs573094033 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325692 | GCAAAAAGCACCGGC[A/G]CGGAGGTCGGAGCTG | 9474 |
rs573111481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190644 | TTTAGAAACCAGCAT[C/T]TACTTAAAAGTGAAC | 9474 |
rs573113109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210440 | AAGTATAAAAATGAA[G/T]GTAGTCTAAGTAAAT | 9474 |
rs573141136 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ATG5 | GRCh38.p7 | 6:106225442 | AATATACTGAGTTGA[A/T]ATTTTTATATTTTAT | 9474 |
rs573151996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318177 | CCTCTTCAAGCACTG[C/T]CCTCTCAAGGAGGAA | 9474 |
rs573243973 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217334 | ATGAAGCTGAAAAGT[A/T]TTGAAATTACAATAT | 9474 |
rs573245870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106282082 | CACAAGAATTGCTAG[A/G]TGAACAGAAAATTTC | 9474 |
rs573287835 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202900 | ACTCCTGAGCTCAGG[A/C]AATCTGCCGGCTTCG | 9474 |
rs573290652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238296 | GAACAAATCATACTT[C/T]TAAGCACAGATTCTC | 9474 |
rs573290777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106246717 | CTCAAAACAGTTTCC[A/G]GACTCTTTGTGAAAT | 9474 |
rs573297772 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106231578 | CCACTATAACACAGG[C/G]AAAGGAAGAAAATCC | 9474 |
rs573309985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106281360 | TTCCCTCATTCCCTT[C/T]CCAAGGAATTACTGA | 9474 |
rs573324193 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106323253 | CGTTTCGCTAAGTGG[A/G]AAAGTCCTTTTTTTT | 9474 |
rs573327769 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106245866 | AACAGAATATCACAA[A/C]CATACAAACTAATCA | 9474 |
rs573329878 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186525 | ATGATTCTGTTCAGG[C/T]AAATAGTTGATCCTT | 9474 |
rs573375122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106303372 | TCAATGAAGAGGAAA[C/T]AGGCAAGCTGAGTAG | 9474 |
rs573384110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106303967 | AAGTTCTAGCTACTC[C/T]AATAAGGAAAAAAAA | 9474 |
rs573398005 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241388 | AAACCTTTGTGCACT[C/G]TTGGTGGGAATGTAA | 9474 |
rs573430874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269514 | AAGGGGTGGGAGGCT[A/C]AGGCATGGCGGGCTG | 9474 |
rs573456109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106274940 | TAAATGGACAAAAGG[C/T]CATGAAAGTTGAAAG | 9474 |
rs573468114 | snp | C/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233320 | GATTCCCAGGTACGG[C/G/T]GAAATAGCCAGACCA | 9474 |
rs573491272 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ATG5 | GRCh38.p7 | 6:106296319 | CTTAATGATCTTATT[A/G]TTTCCTATGTATCAA | 9474 |
rs573507836 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106218134 | CATTCTGTGTCAAAG[A/G]ATTCACTAGCAAAAG | 9474 |
rs573513962 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | ATG5 | GRCh38.p7 | 6:106293858 | TTAAGTCATCCTTTT[-/A]AAAAAATCTAAAGTA | 9474 |
rs573519778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261112 | ATTAGAGTTAAAGAG[C/T]GGGAAAGAAGAGTTG | 9474 |
rs573546741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106289877 | TTGCTTCTATGTTCA[A/G]TATTCTACAATATGT | 9474 |
rs573556440 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ATG5 | GRCh38.p7 | 6:106260262 | TAAAGTATAATTTTT[A/T]AAAAAAGAAAAAATA | 9474 |
rs573565204 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205355 | GAATTTGGAGCTCTC[A/G]TTCATATCCTAATTA | 9474 |
rs573594456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106266866 | TCAAAATAGTAAGAG[C/T]TATTTATGACAAACC | 9474 |
rs573669491 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213139 | ATGATCAGAAGGCAG[C/G]AATAAATTTTATCAG | 9474 |
rs573676613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296023 | GCTTGAACAAAGTAC[A/T]TAATAAACAACTGCT | 9474 |
rs573681016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106210370 | CAATGTATAAATCTT[A/G]TAAGAACCAAAATCA | 9474 |
rs573704188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264830 | GCCTGCCCTACAAGA[G/T]CTCCTGAAGGAAGCA | 9474 |
rs573735200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283968 | CTTCTTTCACTTAAC[A/G]TGGTATTTTCAAGGT | 9474 |
rs573766786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106232749 | ATCTCAGGATTATCA[A/G]TGAGGTCACTGTCCC | 9474 |
rs573773295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106187530 | AACCATCAAGAAACT[C/T]TGTGTTATTCCTTTA | 9474 |
rs573779610 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106210170 | AAATGAGTGAGGAAA[G/T]GTGGGGACTCAAGAC | 9474 |
rs573811938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194458 | ATTTATCTTGTCAAC[C/T]AATTCACTTTATTAA | 9474 |
rs573833874 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259943 | CATAAAAAGGATGTG[C/T]TCATGTCCTTTGCAG | 9474 |
rs573845601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106283426 | TTAGAGACAGGGTCT[C/T]ATTATGCTGCCCAGG | 9474 |
rs573850811 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292778 | GCTGGCCCAAAAACT[C/T]GTAAATTTTAAAAAG | 9474 |
rs573851560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324908 | GAAGGCTTTGGAAGT[C/T]CAGCTACTGTCTGGT | 9474 |
rs573871641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106256950 | AACTTTTGAGTCTTT[C/T]GTAATAACACTTAGC | 9474 |
rs573896125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106217479 | ATTGTGGACTCACTG[A/C]GTCCACTGTTTGCGA | 9474 |
rs573899237 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288871 | AAATTAGAGGAAATA[C/T]GTCTGTTTGAAAACT | 9474 |
rs573905859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106281230 | ATGATTCACATACAG[C/T]GAAATGCAGAAATCA | 9474 |
rs573927898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106231045 | CCCCTTCAACCCAAA[C/T]GGTCCAAAAGGAGAT | 9474 |
rs573954176 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310316 | TTTTCTGTTCCGTTT[A/G]GCCTGTGGGAGTAAT | 9474 |
rs573989071 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185692 | CAGGCTTACAGTGAT[-/A]AAACAACAAAGATGA | 9474 |
rs573992943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106230507 | GGTGAGGGCTGCTAC[A/G]TCAGTGAGCATAACT | 9474 |
rs574010578 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216812 | GAGCCAGGAGTTCCA[C/G]GCTGTACTGCACTAT | 9474 |
rs574034983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106224796 | TGAGGTAGGAGAATC[A/G]CTTGAACCCGGGAGG | 9474 |
rs574080423 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106320481 | TTGGGTTGAGAGTAG[-/T]TATTAATAGATAATG | 9474 |
rs574108778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287926 | AAATGTTAAAAAGCA[A/G]CAAATCCAAGTGAAA | 9474 |
rs574138587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317497 | AACTGGATGCAATGT[C/T]ATCTACAGGTACGTA | 9474 |
rs574144206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244886 | CTTGAAAAACAGATA[C/T]GATGTGCTTAATTTT | 9474 |
rs574174828 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ATG5 | GRCh38.p7 | 6:106192229 | AAGGTTATTTTTTTT[A/T]AAAAAGATGAAAACA | 9474 |
rs574177246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106310486 | CTTCTTGTCTTTTAC[C/T]TGCAGACTATATATA | 9474 |
rs574191745 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297966 | CCTGTCAAAATCTAT[-/T]TTTTTTTTTTTTTTT | 9474 |
rs574193626 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263714 | GATACCCAGGCGAAC[A/G]GGGTCTAGAGTGGAC | 9474 |
rs574209354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191567 | GTTTCCTCATCTTAC[A/G]GTGTGAACAAAGAAT | 9474 |
rs574215191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106259466 | ATTGCATTACTCTAC[C/T]GAGTACTAACACCTG | 9474 |
rs574257343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214466 | AACACTAAAAAATAA[A/T]AATTAACATTTGAAA | 9474 |
rs574276812 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ATG5 | GRCh38.p7 | 6:106246173 | AATGAGAACCTATAT[G/T]GTCCTTAGGCTCTTT | 9474 |
rs574277713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106314408 | CTAAAAATCTAAAAA[C/T]TAACCGAGCATGATG | 9474 |
rs574315338 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266023 | AAGGAGATGGAGACA[A/T]GAAAAACCCTCAAAA | 9474 |
rs574324869 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316598 | TACCTAAAGAGGAGC[C/T]TCACCTATACCCTGT | 9474 |
rs574353333 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242629 | ATAAATAACAACAAC[-/A]AAAAAAAACACCTCA | 9474 |
rs574410901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106233846 | CCCCCTCCATGCTGC[C/T]GTACAACCAGCAGCT | 9474 |
rs574439714 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106221573 | CGCCTGTAGTCCCAG[C/T]TACTAGAGAGGCTGA | 9474 |
rs574454584 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267177 | TATTTGCAAAAATCA[C/T]AAGCATTCCTATACA | 9474 |
rs574475833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106284733 | GGTTTTTTTTGTTTT[G/T]TTTTTTTGCTTTTCC | 9474 |
rs574480601 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106324221 | CAGTACTGAACATGT[A/C]TAGACTCTTTTTTGT | 9474 |
rs574489205 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217895 | ATTGAGATAATAATA[-/AT]ACCACCAATTCATCA | 9474 |
rs574509599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234205 | CACCCCTAGCCCCTA[C/T]AAAGGACTAGATCTC | 9474 |
rs574518611 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ATG5 | GRCh38.p7 | 6:106207533 | CAGAGAGACCTCATC[C/T]CTTAAAAAAAAAAGA | 9474 |
rs574536257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106241423 | GTACAGCTACTACGG[A/G]AAACAGTATGGCCAT | 9474 |
rs574547657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222311 | TGGCTTCTAAAATTA[C/T]CCCATATACTACATG | 9474 |
rs574588241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256335 | GCAACATTTCTTAAC[G/T]TTTGCTTCTCACCAG | 9474 |
rs574597621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106307115 | CTCATCAGCACAAGG[C/T]GAGTTCCAAAATTTC | 9474 |
rs574656282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106291884 | GTTTAATAACATGGT[A/G]TTGTGCAAAGCACAT | 9474 |
rs574660239 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223191 | TCTAATACATAACTT[C/T]TGCTCTCATCTTATG | 9474 |
rs574690793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106298211 | TGATCTGTCCGCCTC[A/G]GCCTCCCAAAGTGCT | 9474 |
rs574697237 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225798 | AAACAATTTTATCAC[C/T]AGGAGAGTTTGTGGA | 9474 |
rs574718801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106323870 | CTCCTAAATGACTTG[A/G]CCCCATTTCCACCTA | 9474 |
rs574726219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312420 | ATAAGACATCTAAGT[C/G]AGGATCTCCAGCAGA | 9474 |
rs574765071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304909 | CCAGCCTGGCCAATA[C/T]GGTGAAACCCTGTCT | 9474 |
rs574765862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106270636 | CTAGTCTATTATGCA[C/T]TCTCCATCTGCTGTC | 9474 |
rs574798501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312791 | AAATGAAAATTAACA[A/G]ACAGACTCTGAGCTT | 9474 |
rs574813968 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192881 | TTCATTAGTAAAACA[C/T]CAACTAATTGAATCC | 9474 |
rs574838778 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301000 | TAAACCAAAATTAGG[G/T]TTTACTTACAAAGTA | 9474 |
rs574893545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106275796 | AGATAAACATGAGCT[A/G]TAGCTTGGTTAACCA | 9474 |
rs574903549 | in-del | -/A | 0.368733 | 0.220005 | intron-variant | ATG5 | GRCh38.p7 | 6:106235813 | AAATATTGCAACTGC[-/A]AAAAAAAAAATAGCT | 9474 |
rs574905288 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326260 | CCCATCCAAGAGTAC[A/G]TATCTTTATCTTACT | 9474 |
rs574937716 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211081 | GAATTATTAGAAATG[C/G/T]TGGTTTATTAAAAAT | 9474 |
rs574951346 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295462 | AATCCAGTGTTTTAC[A/G]TATTCCCTGCCATTA | 9474 |
rs574955849 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207081 | AACTTCCAAGAAACA[A/G]TATTACTCTCATGAG | 9474 |
rs574962824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106298090 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 9474 |
rs574993814 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | ATG5 | GRCh38.p7 | 6:106198769 | TGACAGAGCGAGACC[A/C]TGTCTGGGAAAAAAA | 9474 |
rs575001888 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299208 | TTATATTAAATGGCA[C/T]AGTATTTGCATATAA | 9474 |
rs575010529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106276235 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACGAGG | 9474 |
rs575024431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106198200 | AAAATTTCTGTAGCC[C/T]GAGTTCAAAAATAAA | 9474 |
rs575026268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219403 | GCCACACATCTAACA[C/G]AGTCAGCCCTCCCTA | 9474 |
rs575034429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106319023 | AAATGTGGAGCCAGA[C/T]TGTCTGGAGCCAAAA | 9474 |
rs575037238 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106305640 | AATAAATATAGGAAG[A/G]ACGTTATTATTCAAC | 9474 |
rs575041735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106255291 | TAGGGGAGAGGACAT[A/C]AGCATGATGGGGGAA | 9474 |
rs575064984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106221503 | CCAACCTGGGCAACA[C/T]GGTGAAACCCCATCT | 9474 |
rs575085735 | in-del | -/AA | 0.0126979 | 0.078662 | intron-variant | ATG5 | GRCh38.p7 | 6:106240855 | CATAATGCAGCCATT[-/AA]AAAAGAATAAATTAG | 9474 |
rs575100276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106228513 | ACTCACCGCGTGGCC[A/C]AAGATTCCATTTATT | 9474 |
rs575110657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248435 | ATTTTTTTCTACATT[A/C]TTGCATCCTCTCCCT | 9474 |
rs575155208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106233774 | TAAATCCCCATGGCC[C/T]TCCCTTATCATATTT | 9474 |
rs575191437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106227847 | TACAGAACAGGATAT[A/G]AAATCTTATCAGGTA | 9474 |
rs575193261 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326752 | TTGATAATTGGGAAC[A/G]TAAGGAAAATTCTAG | 9474 |
rs575218055 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ATG5 | GRCh38.p7 | 6:106240159 | TACGCCTGGCTAAGG[A/G]GCCTTTTTAACAGAG | 9474 |
rs575225977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106190727 | TATGATTAGAATGGT[A/G]AGAATTACATATAGA | 9474 |
rs575237812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212638 | CCCAGAGCGAGACTC[C/T]GTATATTAAACAAAA | 9474 |
rs575257665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106311917 | CTCACTGCAACGTCT[A/G]CCTCCCAGGTTCAAG | 9474 |
rs575269278 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ATG5 | GRCh38.p7 | 6:106296854 | AGACTCCATTCTGGA[A/T]TCAGTTTTTAGCTAT | 9474 |
rs575272391 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263459 | TGACTCTGAAGAGAG[G/T]AGCTGATCCTGACAA | 9474 |
rs575292359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106291867 | TCTTTGGTAACTAAC[A/G]TGTTTAATAACATGG | 9474 |
rs575314214 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106213015 | AAAGCTTTGGTTTTA[C/T]CTATGTTTAACAAAA | 9474 |
rs575316140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106274800 | CTCTCTGCCAAAGAC[C/T]ACACTAGGTGCTGGG | 9474 |
rs575320805 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292446 | GGTCTTAAAAACTAC[A/C]GGAATGAACATTTTT | 9474 |
rs575326392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106312976 | GTTGAGAGATGGGGT[C/G]AACAGAAGGTTGTTG | 9474 |
rs575355679 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ATG5 | GRCh38.p7 | 6:106283079 | TACGGGCATGAGCCA[C/T]TGCACCTGGCCTACA | 9474 |
rs575357544 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266570 | AAATTTCAGGCCAAT[A/G]TCCCTGATGAACATC | 9474 |
rs575369480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248318 | ACATGAAGAGATGAA[A/C]GTTTTAAATATCCCT | 9474 |
rs575380038 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311990 | TGTCCACCACCACAC[C/T]GGGCTAATTTTTTGT | 9474 |
rs575381566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106320427 | CAATAAAGGTATTAA[C/G]TGGGCAGGTGCAATA | 9474 |
rs575397147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106262622 | AGACAAACACAGAAG[A/G]CGGCAGGTGATTTCT | 9474 |
rs575414296 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223504 | AATCAAAACTTGCTG[G/T]GTTGGGCTGCCCCCT | 9474 |
rs575415947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106313442 | GACATTGATGACCAT[A/G]GGTCCAATCATGATT | 9474 |
rs575428795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106304741 | TATTATCTTGATTTT[A/G]TAAGTAGCTACACAA | 9474 |
rs575505338 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ATG5 | GRCh38.p7 | 6:106323107 | TTTGTTTGTTTGTTT[G/T]TTTGTATTTTTAGTA | 9474 |
rs575510627 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198743 | ATTGCACCACTGCGC[C/T]CCAACCTGGGTGACA | 9474 |
rs575515402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106219353 | GTATAACATACATTA[G/T]TTTGGCTATTCCAAA | 9474 |
rs575533056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318208 | TAGTAATCTGATTGG[A/T]CAGATTCCAGGACAC | 9474 |
rs575555253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106269668 | AAGCCCCTCATTGCC[C/T]GGGGCCGGCAGGGCC | 9474 |
rs575569780 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236340 | TTTTCATTTTTCTTG[A/G]GTGGAGCTGTTAGAA | 9474 |
rs575594058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106277351 | CTGTTGAAGACACAG[G/T]AATTACAGGACATGC | 9474 |
rs575597762 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106218305 | CTAACTTAAAATATG[G/T]TGTTTTATTCAAATA | 9474 |
rs575597945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240343 | TAAAATATCTTTAAT[A/G]TATTTATAGATATTA | 9474 |
rs575696859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106324692 | TACACTTTCCCCCAA[C/T]TTTAAGTAGCATATC | 9474 |
rs575702078 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323622 | GCTCTCAAAAGTCTA[C/G]AATCTGGTCATTTCG | 9474 |
rs575711757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106271516 | TCCTCTTGGACTCTC[C/T]AGCCGCTAGATTGTG | 9474 |
rs575713894 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222661 | AAAGTAATGAACTTA[A/C]TATATGAAAGGTAAT | 9474 |
rs575714646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106226174 | TAGTTCTAGGCATTC[A/G]AGAAAATCTCTTCTA | 9474 |
rs575715494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189731 | AAACAATATTTTTGG[C/T]AAACATGTCTTTTTG | 9474 |
rs575787775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106296849 | CAAGCAGACTCCATT[C/T]TGGAATCAGTTTTTA | 9474 |
rs575813535 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321707 | AGCTCCTTGGGAAGT[C/T]TTCCCCTATGCAGCC | 9474 |
rs575827592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106301021 | TTACAAAGTATTCTT[C/T]GGAAGGACCAAGAAC | 9474 |
rs575848537 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106225572 | GTTGAATCATTAAAG[C/G/T]GGTGATATCATCAGT | 9474 |
rs575850419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106232468 | CGTTTGTTGTCCCCT[A/G]CTTGAGGAAGGAATT | 9474 |
rs575859242 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106261148 | ATATGCAGAGATAGA[C/G/T]CAAGTGAGCTAGAGC | 9474 |
rs575877542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211435 | GATTGGACAGGCCGG[A/G]CGTGGTGGCTCACGC | 9474 |
rs575886007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106211961 | GTAAAATTTATTTGA[C/T]TTACAAGGGTTGCTT | 9474 |
rs575891281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106300154 | AGTTTACAGAATACA[C/T]TGTTAACTCCTTTAT | 9474 |
rs575966647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315614 | TGAACGTATCGTGTG[C/T]GTGTATGTGTGCATG | 9474 |
rs575968346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106212438 | CTGAGGTCAGGAGTT[C/T]GAGATCAGCCTGGCC | 9474 |
rs576026058 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106249575 | AACACATTTTCGTGT[A/G]GACATATGTTTTCAG | 9474 |
rs576029186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106264657 | CTCTGCAGAAACCCT[A/G]CAAGCCAGAAGACAG | 9474 |
rs576108021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106202764 | CTTTCCAGGTTCAAG[C/T]GATTCTCATGGCTCA | 9474 |
rs576161978 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264230 | CAAACTGATCAAGTG[A/G]AAGAAAGGATATCAG | 9474 |
rs576180133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106305356 | GGTACTCTTCATCTA[C/T]GTCCTACCAACAGGA | 9474 |
rs576214469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106308844 | AATTAAAATGATTCA[C/T]CTGAGTCAATTAAAC | 9474 |
rs576249327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106322130 | TGACGCAATCTACTA[C/G]AAGTAAGTTTCTTGA | 9474 |
rs576266941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106265324 | TAAATATATGTGCAC[C/T]CAATACAGGAGCATC | 9474 |
rs576290171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106242295 | AAAAAAAGGACATTC[C/T]GACACATAATACAAT | 9474 |
rs576303444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106244215 | AAATAACACTGCTAG[A/G]TTGTTTCTATGAAGA | 9474 |
rs576356454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241702 | GCCTCATCTACTCAG[C/T]TGAAGGTCTTACAGA | 9474 |
rs576379119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106250713 | TGAAATCTCAAGCAC[C/T]TAGCATGGTGCATGC | 9474 |
rs576396606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256833 | TAGGACATTACTATA[C/T]TCTACTGTAGACTTT | 9474 |
rs576435062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106216272 | AAGAGAAATGAAAAT[A/G]TATGTTCACCAAAAC | 9474 |
rs576454547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256222 | GAAAGTGTAAAGTAG[A/G]AAACACTATTAATCT | 9474 |
rs576470781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207338 | ACGAAACTTATAAAC[A/G]TTTTAGGAAACCTTA | 9474 |
rs576537481 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ATG5 | GRCh38.p7 | 6:106235477 | GTTTTCCTGTTGAGT[A/G]GGGGGACTGAGAGAC | 9474 |
rs576537802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106299350 | TTCATTTTTATTGTT[A/G]TATTATTATTAGTTA | 9474 |
rs576553095 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ATG5 | GRCh38.p7 | 6:106286126 | ACCCAGGCCTCAGCC[A/T]AGCACCCAGGGAGAA | 9474 |
rs576556562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106229236 | TTAGGCATCTAGGCT[A/C]TAAACCCAGGGAGTC | 9474 |
rs576565625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306548 | TACAGGGTAGCCCAC[A/C]ACAACAAAGAATTAT | 9474 |
rs576600734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200774 | TGAGCCACCACACCC[A/G]ACCAACTCTATGCAA | 9474 |
rs576602559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106208473 | TTTTAATTTCATTCA[G/T]TTACTCTTCAGTTGT | 9474 |
rs576638358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207922 | TATAGTGAAACCTGA[C/T]CTCTACTAAAAATAC | 9474 |
rs576645243 | snp | A/C/G | 3.29925e-05 | 0.00406145 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293060 | TGTTCCAAGGAAGAG[A/C/G]TGAACTTGATGCAAG | 9474 |
rs576680346 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327573 | GGGCATGGTGGCATG[C/T]GCCTACAGTCCCAGC | 9474 |
rs576717107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321643 | GATTACAGGCGTGAG[C/T]CACCGCGCCTGGCCA | 9474 |
rs576728940 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246259 | GCAGGAGGTTCTGCC[C/G]AGAGTCCCCATCTGG | 9474 |
rs576750173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106321600 | CCTGACCTCATGATC[C/T]GCCTGCCTCGGCCTC | 9474 |
rs576756665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106222414 | TTCCTAATTGATGAT[C/T]AGGAAAATAACTTTC | 9474 |
rs576764931 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222383 | GACTTCATGTTTTAA[A/T]GTGATCACTAAAAAT | 9474 |
rs576772703 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282795 | TTACATGGATTGAGA[C/T]TTTTTTATTTTGAGA | 9474 |
rs576784095 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106221903 | TGTCTTATTATTATT[A/T]TTTTTTGAGACAGAG | 9474 |
rs576784805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106193217 | TCAGAAAAATACAAA[C/T]CCATTTAAAAATACT | 9474 |
rs576820580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106192485 | TCTAGTGAGATGCTT[C/G]AGTTTCCTTCTTACT | 9474 |
rs576824286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106200621 | CTGGAACTACAGGCG[C/T]CCCGCCACCACGCCC | 9474 |
rs576849955 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243012 | TTCTGGAAACAAAAC[-/AA]AGAGTCTAAAATTTG | 9474 |
rs576852944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106269818 | CATGCTGAGGGAGCC[A/G]GCTCCAGCCTTGGCC | 9474 |
rs576899953 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286554 | CACCTGGTATTCCTA[C/T]CTTTCTATAATCCCT | 9474 |
rs576905948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106320731 | AAATCTATAAATGTA[A/G]ATAAAATGAGACTAG | 9474 |
rs576957114 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326860 | TACAGTACATTAGTG[A/G]GTATCTAAATCAAGT | 9474 |
rs576971726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106215339 | TAGTGGAGCTCTTCA[A/C]ACAGTCTCACCTACC | 9474 |
rs576984442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106285470 | TCTAGATTATACTGT[A/C]TTCCTTTAAGATGCT | 9474 |
rs577001506 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326309 | GGCCGGGCGCGGTGG[C/T]TCACGCCTGTAATCC | 9474 |
rs577004172 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301386 | ATAAGCAATTAGAGA[C/G]AACAGATAAGATGGG | 9474 |
rs577035675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106264502 | AGAACACCACTAAGA[C/T]ACTCCTAAAGAAGAG | 9474 |
rs577075624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106263994 | GGATGAAGAATGAAG[C/T]TGATGAATTGACAGA | 9474 |
rs577113177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106214524 | TTAATCTCCAAAGGA[A/G]AAGTTTCTTAATTGA | 9474 |
rs577124495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106256096 | AACAAAAATATTTTA[A/T]TTTTTGAAAGACTGA | 9474 |
rs577152818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106291976 | GAAGGAAAAGCATCA[A/C]ATGAAGAATGAATGA | 9474 |
rs577164187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106248673 | GGGTGCAGTGGCCCA[C/T]GCCTGTAATCACAGC | 9474 |
rs577250286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106252303 | GAAGGCTATCAAATC[A/G]AAAGCATAAAACTGA | 9474 |
rs577276861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106268989 | CACCATGGCACATGC[A/G]TACCTATGTAACAAA | 9474 |
rs577285647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106206512 | AAAATTAGCTGGGCA[C/T]AGTTGTGGGCGCCTG | 9474 |
rs577330411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106258735 | ACATTCAATGTTCAG[C/T]CAATTCAGGATAACT | 9474 |
rs577336949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106306494 | TGCTACTGGCACTTG[C/T]AGGAAGAGGCCAGAG | 9474 |
rs577359512 | in-del | -/C | 0.0071798 | 0.059484 | intron-variant | ATG5 | GRCh38.p7 | 6:106250989 | CAATGTCCAGATACG[-/C]CAAGTCTCTCAGCAA | 9474 |
rs577379797 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257173 | GCAAAGTCTTTAGGG[A/G]CAATAACATGAGTGA | 9474 |
rs577390175 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241399 | CACTGTTGGTGGGAA[C/T]GTAAAGTGGTACAGC | 9474 |
rs577397852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106241511 | ATACCCCAAATAACT[A/G]AAAACAGGGTGTACA | 9474 |
rs577422380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106240917 | CAGCACTTTGGGAGG[C/T]CAAAGCAGGCGGATC | 9474 |
rs577427417 | in-del | -/A | 0.477684 | 0.103247 | intron-variant | ATG5 | GRCh38.p7 | 6:106320625 | CAAAAGGCTGTTCTG[-/A]AAAAAAAAAAAAATC | 9474 |
rs577434130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106249192 | TAGTGGTTTTCAGTA[C/T]ATTCAGAGTTCAGAA | 9474 |
rs577450077 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226214 | TGATCACTAAACTCA[C/G]CAAGCAGTAACTTTA | 9474 |
rs577458615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106212187 | AAGTGAAAAAGACTG[C/T]TCTCATTTTTGTACA | 9474 |
rs577461829 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259769 | TTAAAATACCTGTGG[A/G]ACAAAATCTAAGCAT | 9474 |
rs577464025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106292426 | GGTCACACTAAATTC[A/T]GTCTGGTCTTAAAAA | 9474 |
rs577465462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106191688 | CAATAACACGAGTGA[C/T]TCTTCTCCACCCCTC | 9474 |
rs577508086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106234226 | ACTAGATCTCTTAAA[A/T]CTACATGAAACCCTC | 9474 |
rs577561862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106245068 | TAGAATACTGGCTAA[C/T]ATGAAGCACCTGGAC | 9474 |
rs577574984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189819 | AATGACTCAGGAGAA[A/T]AATGTTACTGTATGC | 9474 |
rs577588781 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234853 | ATGGAATGGGTTGCC[A/G]ACTCCCTGGTCACCT | 9474 |
rs577595256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106229875 | CTCACCGGTTCAGAA[G/T]TATTCTAAGTCAAAA | 9474 |
rs577602086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106310421 | AGATACAATTTACCT[A/T]GGAAATATTTAAACA | 9474 |
rs577643810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106207219 | TGGCTGCTCCCATCT[C/G]TCCTCTACTCATGTG | 9474 |
rs577659659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203708 | ACCTAAGCCTCCAGA[C/G]TAGCTGGGACTACAG | 9474 |
rs577672496 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106251438 | AGACACTCTTTTATC[-/AG]AGTTTATTAATTCTT | 9474 |
rs577677072 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ATG5 | GRCh38.p7 | 6:106265932 | TAACATCACAATCAA[A/T]AGAATTAGAGAAGCA | 9474 |
rs577684810 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106203330 | TGAGCCAGTGTCTAT[G/T]AAGAGCACCACTGTT | 9474 |
rs577705218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302162 | GAAGTATGAGCTACA[A/G]GAGGGAATATATGAA | 9474 |
rs577726652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106189042 | TAGCATGGTACCTGA[A/C]ATATACAGTAATTAG | 9474 |
rs577745538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106302984 | GTAAATTTTGTTACA[C/T]GCATTTTACTACAAT | 9474 |
rs577749054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238933 | AAAAGTGGAGGGGGG[A/G]AACCCAATAACTTCA | 9474 |
rs577752087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106201601 | TTTCAGTATTATCAA[C/T]TTTCAAATATCAAAA | 9474 |
rs577767528 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106309727 | TCTTTCAGAAATGAC[A/T]AATACAGATGTGACA | 9474 |
rs577769396 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261563 | GGCAGTGATAATTCA[C/T]GTGAAGTACCCAGAA | 9474 |
rs577772475 | in-del | -/AA | 0.0735579 | 0.177111 | intron-variant | ATG5 | GRCh38.p7 | 6:106216962 | AGTAAGCTGTTATTA[-/AA]AAAAAAAAAAAGTTA | 9474 |
rs577782815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106238237 | GTACAGTGGCATGAT[A/C]TTGGCTCACCACAAT | 9474 |
rs577799228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106224686 | TTCAAGACCAGCCTG[A/G]CAAAGATGGAGAAAC | 9474 |
rs577821646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106224164 | AACAGAGTCAGATAA[C/T]AAAAGATCAAAGATG | 9474 |
rs577826726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106237308 | AATGCTCCAATGAAA[C/T]CTTCATTAACTGAAC | 9474 |
rs577867451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106188469 | TACTATGAAACAGCA[C/G]AAGAAACAAGTCACA | 9474 |
rs577899739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106288735 | AGAAACTGCACTTTA[A/G]TAAGAGACACAGGTA | 9474 |
rs577919482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106194416 | ATTTATATGTTTCTT[C/T]TTCTAACTGCTTCAT | 9474 |
rs577930222 | snp | C/G | 3.31967e-05 | 0.00407397 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186521 | AAGGATGATTCTGTT[C/G]AGGCAAATAGTTGAT | 9474 |
rs577939997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106236069 | TATTAGTTTTGTCTG[C/T]TCTAGAACTTCTTAA | 9474 |
rs577975986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106244164 | TTATTAGAAAACAAG[C/G]ATTGTTTTATCAGCT | 9474 |
rs577978131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106209764 | TGCAAGATGTTAGAA[C/T]TGGGGGAAACTAGAT | 9474 |
rs577984691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106235522 | TTCCTAGGCCGACTA[A/G]GAATCCCAAAGCCTA | 9474 |
rs578000551 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | ATG5 | GRCh38.p7 | 6:106190396 | CTCATGACTTAAACA[-/C]CCCCCCAAAAAGCCT | 9474 |
rs578021470 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATG5 | GRCh38.p7 | 6:106293788 | CAGTGAAGTAAATAA[C/G]TTAGCAATAAATAAA | 9474 |
rs578025759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106203814 | CATATTTTATAAGAA[C/T]ATGACTTCAAACACT | 9474 |
rs578035943 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ATG5 | GRCh38.p7 | 6:106294213 | ACAGTCCTGTCTTTA[C/T]CTGTATAATCTATTA | 9474 |
rs578040530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106279312 | TGGAGGTATCTTTGT[A/G]CATACCCAGAATTTT | 9474 |
rs578059832 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294383 | AGCCCTGCACTGCAA[-/G]GGAGCAGTACACATT | 9474 |
rs578094369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106323207 | CTCCCAACAAAAAGT[C/T]CTCCTATCATTATCA | 9474 |
rs578111817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106315878 | GGAAAACAAAGTCCA[A/G]AACGCATCATGACAA | 9474 |
rs578134552 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289776 | CAGAACAACAACAAC[-/A]AAAAAAAACAGGAAC | 9474 |
rs578141453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106287104 | AAACAGCTACCAACA[G/T]TTATAGCTGGGAAGT | 9474 |
rs578145282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272760 | TAATCCACACTACTA[C/T]GGTCCGGGCATGATT | 9474 |
rs578148430 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211436 | ATTGGACAGGCCGGG[C/T]GTGGTGGCTCACGCC | 9474 |
rs578155575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106265493 | GAACTCAGCTCTGGA[C/T]CAAGTGGACCTAATA | 9474 |
rs578183158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106272179 | GATATGACCACTGGT[A/C]TAGACTCCCACTTGG | 9474 |
rs578203483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ATG5 | GRCh38.p7 | 6:106187444 | TTTTAAAGTAAATAT[A/G]AAGATTTTTGTCATA | 9474 |
rs578222981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ATG5 | GRCh38.p7 | 6:106271448 | GGACACAAAGAGAAG[A/T]TAGCTATGAATCAGG | 9474 |
rs578255219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106280288 | TCAAAAAAAAAAAAA[A/G]AAGAAAGAAAAGAAA | 9474 |
rs745316070 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106186933 | TTTCTTAATTACTGT[A/G]CTTACTTAAGATTGA | 9474 |
rs745317369 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320806 | TCATCCACCAGTCCT[A/G]TAGTGCCTACCGGTT | 9474 |
rs745346448 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273045 | TACAATGTAATCTCA[A/G]TGTTCCAAAGACTGA | 9474 |
rs745353435 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228819 | TAGACTCAGGTATGA[A/G]GCTATCTGGGGAAGG | 9474 |
rs745356421 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216447 | TGATACATGCTACAA[A/G]ATGAATGAACCTTAA | 9474 |
rs745414973 | in-del | -/TTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307536 | TTGATTTCAATACCC[-/TTT]TTTTTTTTTTTTTTT | 9474 |
rs745476585 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200885 | AGCAGGACATTTTAC[-/AC]ACACACACACACACA | 9474 |
rs745507288 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185378 | TAGCTCACAAGAAAT[G/T]AAATGTAATGCACAA | 9474 |
rs745551266 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228182 | ATGGGAGCTCTGTTT[C/T]CACTCTATTAAATCT | 9474 |
rs745559235 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271993 | CCTAAACTGCTTCAG[C/G]TCTTCATTTAATGTC | 9474 |
rs745569063 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288673 | ATTACCTATGCACTT[G/T]TAAGAAATGCAGAAT | 9474 |
rs745604079 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282532 | AGAACACATACGATG[A/C]ATTATGGAAGTGCTT | 9474 |
rs745608537 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321451 | GCAAGCTCCGTCTCC[C/T]GGGTTCACGCCATTC | 9474 |
rs745671150 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266948 | AACGGCCACAAGACA[A/G]GGATGCCCTCTCTCA | 9474 |
rs745680616 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284214 | CTAGGAATAGAACTG[C/T]TGTGTAATGTGGTAA | 9474 |
rs745688865 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235411 | ACTATGCCCCAATTC[C/T]GCAGGAAGCAGTTAG | 9474 |
rs745734866 | snp | C/T | 1.6795e-05 | 0.0028978 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279683 | CAATCCCATCCAGAG[C/T]TGCTTGTGATCTTTT | 9474 |
rs745751022 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218875 | AAAGCTTTGCTTTTA[A/G]AAGAAAACTTCAAAA | 9474 |
rs745781448 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299004 | ACCCACAACACAGAA[A/G]CCACATATACCCTAA | 9474 |
rs745796774 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322997 | CAATCTCGGCTCTCT[C/G]CAAGCTCTGCCTCCC | 9474 |
rs745803052 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295425 | AGATAAGATTCACTC[A/G]AGATCACATAAAATT | 9474 |
rs745833388 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296601 | GGCGGGTGGTTCACC[G/T]GAGGTTAGGAATTCA | 9474 |
rs745840246 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214644 | TTATAATTCTGTCTA[C/G]ACAGTGCCAAATGTA | 9474 |
rs745859061 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205632 | TACATATTAAAAAAC[A/G]GAAATTCTTCTCTAA | 9474 |
rs745861858 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261836 | ACAATTATTACCGGG[C/G]GAGCGGGCAGTGTGC | 9474 |
rs745879329 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184564 | CAGCATGAATTTCTG[C/G]TTTTACTCTTCCTCT | 9474 |
rs745882527 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249131 | ATAAACAACTTGAGA[C/T]ATAATTTGCATACCA | 9474 |
rs745907340 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189939 | AACTTCTTTATATAG[A/G]GCACTTTTTAGAGAG | 9474 |
rs745915392 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278353 | GCCTTGGTGAACTGA[A/C]GTCATTTTTCTACAT | 9474 |
rs745924832 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246248 | TTAAAGATCAAGCAG[A/G]AGGTTCTGCCGAGAG | 9474 |
rs745939615 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279323 | TTGTACATACCCAGA[A/C]TTTTCCACTGTGACC | 9474 |
rs745961972 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202732 | AGTGGCGCGATCTCA[A/G]CTCACTGCAACCTCT | 9474 |
rs745970597 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247413 | CCTCATGCAAATATG[C/T]TGTGAGAAAGACTTA | 9474 |
rs746030454 | snp | C/T | 3.48159e-05 | 0.00417214 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308417 | ACTAATGTCTTCTTG[C/T]CTCATAACCTTCTGA | 9474 |
rs746048098 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199684 | AAATTATTTAACTAA[A/G]ACTCTTATTGAAAGC | 9474 |
rs746076268 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285341 | ATTCTCTTAGGTCAG[C/T]TTCTATTGAGAGTAA | 9474 |
rs746078875 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306012 | GTCATATAGCTACAA[C/T]GAGCTTACAGCATGA | 9474 |
rs746142360 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292362 | AGCAGAAGCAAGGTG[A/G]CTAAGGGAATGAGGG | 9474 |
rs746153578 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260280 | AAAAGAAAAAATAGC[A/C]ACAAAATCTTGACAT | 9474 |
rs746205394 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265669 | TCTCACAGACCACAG[C/T]GCAATCAAATTAGAA | 9474 |
rs746232505 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222315 | TTCTAAAATTACCCC[A/G]TATACTACATGCATG | 9474 |
rs746256285 | snp | A/C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253724 | AGTATAAATCATCAA[A/C/T]GAGTAAATTTTCAAA | 9474 |
rs746265088 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239813 | AAGCCTATCATTTGC[A/T]AATTGTCTATAAATA | 9474 |
rs746287601 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211336 | ATTAAAAGCCAAGCA[C/T]GGATGGAGGTGCTGG | 9474 |
rs746306169 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202055 | GCAGCCACAGGACGA[A/G]ACAGCTTCTGAATGA | 9474 |
rs746331136 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312444 | CAGCAGACAAATATA[C/T]AGGTTTGGAGCTCTG | 9474 |
rs746396244 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant | ATG5 | GRCh38.p7 | 6:106201947 | GAAAATGAAAGAAAT[A/G]TTTTAATGTTGCTGA | 9474 |
rs746401086 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191106 | AATCTAGCTGACCAT[C/T]AGAATCATGTGGGAA | 9474 |
rs746404554 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299660 | GTTTTTTATTCATTA[C/T]TCCATTTATGTGTGT | 9474 |
rs746408070 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313649 | CTCAGTGATAAACAT[A/C]TAGGATATAGGCGGA | 9474 |
rs746453609 | in-del | -/ACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263783 | TAACAAAAAGAAAAT[-/ACA]ACATCAACATCAACA | 9474 |
rs746460014 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310981 | TCTGATACAAGTGAT[G/T]CATTTTTATCTATAC | 9474 |
rs746461431 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296881 | CTATCATTAACACAG[C/T]TGAAAATTCCAAGTT | 9474 |
rs746473711 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298553 | AGACTCCATCTCCAT[-/A]AAAAAAAATAAATAA | 9474 |
rs746480039 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206522 | GGGCATAGTTGTGGG[C/T]GCCTGTAATCCCAGC | 9474 |
rs746492975 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236452 | CACTCCTACTAATAA[C/T]GTATGAGAGTTATAT | 9474 |
rs746501994 | snp | A/G | 5.0255e-05 | 0.00501248 | intron-variant | ATG5 | GRCh38.p7 | 6:106248123 | AGGCTTTCATAAATG[A/G]ATGTTTTTTAAAATG | 9474 |
rs746533448 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188090 | GACCATAGTGTTAAT[A/G]TAATGATTTGTTTTC | 9474 |
rs746541331 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319634 | ACCTTTCTTCTACAC[-/AT]GATTCAGGCAGAACT | 9474 |
rs746543019 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250422 | CAATTTCACAGATGA[C/T]AACTAAGGCCCAGAT | 9474 |
rs746564375 | snp | A/G | 3.30049e-05 | 0.00406219 | missense, stop-gained, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202085 | AAAGGTCTTTCAGTC[A/G]TTGTCTATTTGAAAA | 9474 |
rs746571413 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219999 | TTCTCTGAACCAATA[C/T]TGACCCTCCTTTAAA | 9474 |
rs746580119 | in-del | -/AACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297756 | ACACACACACACACA[-/AACA]CACACACACATATAT | 9474 |
rs746580568 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229638 | ATTGAAGGTCTTCTC[C/T]GCGACCCTATAACAC | 9474 |
rs746611194 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321141 | TCCACCTATTAGTTA[C/T]GTGTCTTGAACAACA | 9474 |
rs746625951 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188416 | AGAGTAAAAGTTCCT[C/T]ATCTCTAAAGTTTTT | 9474 |
rs746680679 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200604 | CTCAGCCTCCCAAGT[A/G]GCTGGAACTACAGGC | 9474 |
rs746695261 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247930 | TAGTAAGCATGTGAA[C/T]CTGCCAATATGAAAT | 9474 |
rs746697798 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106186968 | AATGAAACTGTAGTG[A/G]CAAAAACAGCCCATT | 9474 |
rs746723418 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275033 | CATCAGTGCTGGATG[A/T]TCACTAGCCCCTAGC | 9474 |
rs746740510 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285139 | TCCAAACTGGGTAAC[G/T]TCTATCGATCTGTCT | 9474 |
rs746742062 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268216 | CATCAAAAAGTGGGC[A/G]AAGGATATGAGCAGG | 9474 |
rs746747965 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196316 | GTTATTTTAAACTAA[A/G]CCAAAAAGTTAAAAA | 9474 |
rs746804276 | in-del | -/GATTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200925 | TTGGTATTCATGAAG[-/GATTT]GATTGGTTCAAGGAT | 9474 |
rs746828337 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260143 | GGGATAGCATTAGGA[A/G]AAATATCCAATGTAA | 9474 |
rs746834947 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226751 | TGTATCATTCCCAAA[C/T]AGAAATAGAAATTAT | 9474 |
rs746835397 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270363 | GAAGTTGTAGATTCT[C/T]AAATGCCACACACAG | 9474 |
rs746894949 | snp | A/G | 1.64982e-05 | 0.00287208 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293064 | CCAAGGAAGAGCTGA[A/G]CTTGATGCAAGAAGA | 9474 |
rs746901779 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230550 | GAGGTCCATGGGTGG[-/T]TTACACACCCCGGAA | 9474 |
rs746939016 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282845 | AGGCTGGAGCACAGT[A/G]GCACAATCACACCTT | 9474 |
rs746952269 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321356 | TTTATCCTCTCTGGG[C/T]CAACTCTTTTTTTTT | 9474 |
rs746966283 | snp | A/T | 5.3592e-05 | 0.00517621 | intron-variant | ATG5 | GRCh38.p7 | 6:106279848 | GAAAAAATATACATA[A/T]AAAACAGGATACACA | 9474 |
rs746978531 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315859 | CATACCCACATACAT[A/G]TAAGGAAAACAAAGT | 9474 |
rs746985719 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251803 | GAAAATCAGTGTTGA[A/G]ATTGAAGGAATAACC | 9474 |
rs746996150 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284287 | TACACCATTTTACAT[G/T]CTCATCAGCAACGTG | 9474 |
rs746996590 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208246 | AACACATATGTGTAT[A/T]TATACATCTGTGTAA | 9474 |
rs747018388 | in-del | -/TTTTAGGGGAAGAATGTTGTTATTATGTTA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234962 | GGGGAAGCTGTTTAT[lengthTooLong]TTTTAGCGGAAGAAT | 9474 |
rs747024894 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313782 | TTATCTGAACTACAG[A/C]TATATTGGCACTAAA | 9474 |
rs747051724 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185247 | TTCAGCATTTGTATA[A/G]TTTTTTATAAGAAAA | 9474 |
rs747063263 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265733 | ACTACATGAAAACCG[C/T]TCCTAAATAACTACT | 9474 |
rs747072627 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264314 | AGAATAAAAAGGAAC[A/G]AATGAAGCCTCCAAG | 9474 |
rs747074145 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233276 | CAACTAAGAGGATTC[C/T]TTGACATAACAGGTT | 9474 |
rs747155799 | snp | A/G/T | 3.31286e-05 | 0.00406982 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186558 | ATCTGTTGGCTGTGG[A/G/T]ATGATACTAATATGA | 9474 |
rs747229109 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191430 | AGAGTAGAGGATCAC[G/T]AACACGTCTCCCAGT | 9474 |
rs747229447 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205056 | TTGATCTTCAGGCCA[C/T]GAAGAAGCTTTTAAT | 9474 |
rs747253760 | snp | C/T | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316157 | ATAGCGTGAAACAAG[C/T]TGGAATTCGTCCAAA | 9474 |
rs747259438 | in-del | -/AAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309101 | CCGACAAGTAGATAA[-/AAG]AAGGAGCTTGGCAAA | 9474 |
rs747293787 | in-del | -/TTAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195356 | TCTTTCGCTTTCAAC[-/TTAAG]TTGAATGCAGGTGTG | 9474 |
rs747298484 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282333 | AATGCCATATTTATT[A/G]TAGTATTTATGCATT | 9474 |
rs747324313 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247495 | CAAACAGACTTAGTA[A/T]ATTCTTGTGATTTGC | 9474 |
rs747326535 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283690 | GTAGCTGGGACAACA[-/G]GCATGTGCCACCGCG | 9474 |
rs747341318 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291132 | GCAACCAAAAAATTA[C/T]GCAAGTGCTTTTCCT | 9474 |
rs747346752 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290600 | AGGACTGCAGGTGTG[A/G]GGTATCATGCCCATC | 9474 |
rs747347886 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255115 | ATCTCCAGCCATATC[A/G]TGTAACGGTGGGAAT | 9474 |
rs747347988 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241225 | CAAAAATGGGCAAAG[A/G]ACTTGAATAGACATT | 9474 |
rs747370856 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212262 | ATTTTAGAAAAACTA[C/G]ATTTTACAATTTATA | 9474 |
rs747380876 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273254 | TAAAGACTCAAAATA[A/G]ATACACAGGTAGTAG | 9474 |
rs747386754 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205869 | GTTTCTCATTTAATG[A/T]AAATCTTATTTTAAA | 9474 |
rs747417077 | snp | C/T | 1.66521e-05 | 0.00288544 | intron-variant | ATG5 | GRCh38.p7 | 6:106308514 | GAAAATTTGTAAAAC[C/T]GTATTTATTTACTAG | 9474 |
rs747418850 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211422 | TTATTTAAAAAGAGA[C/T]TGGACAGGCCGGGCG | 9474 |
rs747426400 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228971 | ACTCCCGGCATTAGC[C/T]GGTTGAGATCATGTC | 9474 |
rs747445244 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293488 | AGAACTTAAAATTTT[-/A]AAAAAACTGTAAGAA | 9474 |
rs747457173 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223943 | AGTTAATTCTTCCAG[C/T]CTCTATGGCTCTAAT | 9474 |
rs747461511 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300695 | ATACTCTAGACAACT[A/G]TAACACAATGATAAG | 9474 |
rs747481989 | snp | G/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325823 | GAGATGACGTCACGA[G/T]ACCCCACGTGGTCCG | 9474 |
rs747550984 | in-del | -/AG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314004 | AATCATGACTGTATA[-/AG]AGGTTTCTCTGGGTG | 9474 |
rs747592029 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232252 | CCTGTCCCAGACAAC[A/G]GTCCTCCAGAGCTGT | 9474 |
rs747654513 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221142 | TAAGGTATAGGCTAC[A/C]TCTGGCGTATATTAT | 9474 |
rs747679942 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209229 | TATACATGAACGTTC[A/G]TAGCTGTTTTATTCG | 9474 |
rs747683514 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237425 | TAATATGCACATGCA[A/G]TATATACTATTTTGA | 9474 |
rs747729674 | snp | C/T | 1.90326e-05 | 0.00308479 | intron-variant | ATG5 | GRCh38.p7 | 6:106279616 | GTTATGGCTGTATCA[C/T]ATTTTATAAAGTGGT | 9474 |
rs747742228 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209427 | TGAAAAAAGTCAATC[G/T]CAAAAGGTTACACAC | 9474 |
rs747747359 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311251 | CTTCCCCTTATACAG[C/T]ATACAGGTTAGACAG | 9474 |
rs747747963 | snp | A/G | 1.65072e-05 | 0.00287286 | synonymous-codon, missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106248171 | TATTCTAAAGGGGAT[A/G]TAACGAAATCCATTT | 9474 |
rs747790525 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189519 | CCAGCTACTTGGGAG[A/G]CTGAGGTGGGAGGAT | 9474 |
rs747842925 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211146 | CACTGACTGTGGAGT[C/T]AATGTCCATAAAGAG | 9474 |
rs747847318 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279370 | TAAGGAATAAAGACC[A/G]CATCCTTAGAGTAAT | 9474 |
rs747855875 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258015 | CACAAGAGATTGTTC[C/T]TTTCACTTAACATGT | 9474 |
rs747857399 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250742 | GCATAGTATGTGCTC[C/T]TGAATCAAAGAATGG | 9474 |
rs747871535 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184954 | ATACAAGTCAGTGGA[C/T]TTTTTATCCTTACAT | 9474 |
rs747883931 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307100 | ACTCATTCTTGGGAT[C/T]TCATCAGCACAAGGT | 9474 |
rs747907728 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234435 | TTTTAGTAGGACCTC[-/TT]GTTTCCAATCTGGAA | 9474 |
rs747963627 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215239 | AAAAGCAGCTGTGCT[A/G]ACCTCAAAAGTGAAA | 9474 |
rs747968974 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259146 | CTGTTATATAACAAC[C/T]AATTCACTGCAAAAC | 9474 |
rs748014991 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239419 | TATCAAAATTTAAAT[A/C]GAAATTTAATGTATT | 9474 |
rs748058789 | snp | C/T | 1.69827e-05 | 0.00291394 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308377 | ACCATTTCAGTGGTG[C/T]GCCTTCATATTCAAA | 9474 |
rs748085934 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317521 | GTACGTAAACTGCAA[C/G]AGGTGGAAAAAATAT | 9474 |
rs748091324 | in-del | -/CACATACT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242130 | ATCTATATCTATACA[-/CACATACT]CACATACTCACACAC | 9474 |
rs748121771 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315638 | GTGCATGTTTATATG[C/T]TCTTTAAGCTATAAA | 9474 |
rs748143047 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270518 | CATATTTCATTGCTT[G/T]GTATGACTGTGACAC | 9474 |
rs748157600 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196462 | GGCACAATCATGCAA[A/C]AATTAAGAGAGTGAA | 9474 |
rs748193538 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255551 | ACAACATCTTTAAAC[A/G]TATTCCAAGAGTCAA | 9474 |
rs748202278 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323184 | CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAC | 9474 |
rs748245398 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224155 | CCAGGAGTTAACAGA[C/G]TCAGATAATAAAAGA | 9474 |
rs748260597 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239941 | CTTAGTTTATATAAT[A/G]AAAGATCAGCTATCT | 9474 |
rs748287255 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219570 | TGAAATATTATAAGT[-/AA]AATCTACAGATAATT | 9474 |
rs748291103 | in-del | -/AAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240402 | ATAAAATAAAAAGTT[-/AAG]AAGAAAAGATAGGCA | 9474 |
rs748337769 | snp | A/T | 3.38667e-05 | 0.00411488 | intron-variant | ATG5 | GRCh38.p7 | 6:106186708 | ACCCAACAACAATAA[A/T]AGTCAAAACAGTTGA | 9474 |
rs748346595 | snp | A/T | 1.65677e-05 | 0.00287812 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186598 | TCCGGGTAGCTCAGA[A/T]GTTCACTCAGCCACT | 9474 |
rs748364830 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281206 | TAAACTTTTTTAAAA[G/T]TCAAACTTATGATTC | 9474 |
rs748371836 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194334 | ATTATCTCAAATCAC[A/G]AGATACTAACAAGCT | 9474 |
rs748396989 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296555 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9474 |
rs748415546 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282489 | AAGTCCTGTGGTTTT[G/T]ACTGTACAATTTTTA | 9474 |
rs748415668 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265756 | TAACTACTTGGTAAA[C/T]AACGAAATTAAGGCA | 9474 |
rs748421120 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193031 | GATATAGCCAAAGAA[A/G]TACATCAAACGCTGA | 9474 |
rs748445794 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206240 | TTGTAAGGCTTTTGC[C/T]CCTTCTGCCATGTTG | 9474 |
rs748450582 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322355 | CTGACAAAACCCCCA[A/C]CTACCTAGAAATATC | 9474 |
rs748461461 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277767 | TGCAGTGAGCTGAGA[C/T]TGTGCCACTGCATTC | 9474 |
rs748461560 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225003 | AGGCATGACAAGCCA[C/T]CATCATTGCTGTTAA | 9474 |
rs748474570 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250303 | AAAAGACTGTGACAG[C/G]CTTTAGGCCTTCCTT | 9474 |
rs748527557 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244263 | TAACCTTAAGAATAA[C/G]ATGTAGAACAAAGTA | 9474 |
rs748577802 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313824 | TAATTCTAAGACTAG[C/T]CATCACTGATGTTTT | 9474 |
rs748603862 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213759 | TACATCAACCTTTGG[G/T]AGTACTGTTTCTGAA | 9474 |
rs748669804 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289862 | TGGATTACCTTAAAC[G/T]TGCTTCTATGTTCAA | 9474 |
rs748671995 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242341 | GGACATCATGATATG[C/T]GAAATAAGCCTGTCA | 9474 |
rs748683452 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321312 | CCCCTCTGCTTGAAC[A/G]CTTTTTCCCTCCTCT | 9474 |
rs748692314 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184302 | TTCCTAGGAGGTCAC[C/T]ATTTACTATTAGTCA | 9474 |
rs748694069 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270765 | TCTCAAATAGGCTTT[A/C]CTTCCCATCTCATTA | 9474 |
rs748700924 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291232 | TAAAAAGACATGTAC[G/T]TAAGAGTCAAAATTA | 9474 |
rs748703750 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199715 | TAAAATTACACAGTA[A/G]TAAAGATGGATTAGG | 9474 |
rs748710589 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235369 | CGAACGCACCCCTCC[C/T]GAGGAAATCTCAACT | 9474 |
rs748718301 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265169 | AAGCAAATGGAAAGC[-/AA]AAAAAAAAAAAAAAA | 9474 |
rs748754051 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197611 | TCACTGTTTTAGTTC[C/T]CACAAGAGCTGGTTA | 9474 |
rs748771480 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239571 | AACAGATATCAGAAC[A/G]CTAAAATTAAATAAA | 9474 |
rs748818647 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256317 | GGAGATGCAGTATGC[A/C]ATGCAACATTTCTTA | 9474 |
rs748824410 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240916 | CCAGCACTTTGGGAG[A/G]CCAAAGCAGGCGGAT | 9474 |
rs748824955 | snp | A/C | 1.73177e-05 | 0.00294254 | intron-variant | ATG5 | GRCh38.p7 | 6:106279829 | CTGGAAAACTCTATC[A/C]AAGGAAAAAATATAC | 9474 |
rs748892277 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196645 | ACAAGATTGCTTGAA[C/G]CTGGGAGGCAGGGGT | 9474 |
rs748896105 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251568 | TAACTTTAATCTTCT[C/T]ATAGAAACGCTATAT | 9474 |
rs748897344 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209623 | TATAGGGTGAATTTA[C/T]ATATGTGATAAAGAT | 9474 |
rs748972604 | snp | G/T | 1.79664e-05 | 0.00299714 | intron-variant | ATG5 | GRCh38.p7 | 6:106279651 | TAAAATTAAACACTA[G/T]TATACTTACCATTTT | 9474 |
rs748979781 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300486 | ATGTTTAAGATCAAC[A/G]TCAATACAGCCATGG | 9474 |
rs749040612 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318677 | AAAGGTATAATGTAG[C/T]AGAGCTGATACAAAT | 9474 |
rs749046081 | snp | G/T | | | utr-variant-5-prime, intron-variant | ATG5 | GRCh38.p7 | 6:106325343 | CCAACCGGCCCCAGG[G/T]CTCCGGGCCGGCGTC | 9474 |
rs749064730 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260828 | ATATACAGAATTTTA[A/G]CAGCCAGAATTCATC | 9474 |
rs749064745 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247561 | AAATCATCGCTCCTG[A/G]GGGAATACAAGGTTA | 9474 |
rs749190259 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216491 | GCAAAAGAAACCAGA[C/T]ACAAAAGGCCATATA | 9474 |
rs749223333 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307291 | AATTTGTATTTTTCA[A/T]GTTTCATTTAAATCT | 9474 |
rs749268728 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305870 | AAAACTGCTATTACT[A/G]GAAGCAAAGAGAGAA | 9474 |
rs749277962 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219666 | AAACATCAGTAGAAT[C/T]TGGTAACCCAGGGAG | 9474 |
rs749282307 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185252 | CATTTGTATAATTTT[A/T]TATAAGAAAAACATT | 9474 |
rs749307092 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279064 | CCATGGAAAGGGAGG[A/C]CTATCTGTACATAAA | 9474 |
rs749327817 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200124 | GCTAGTATAAGCAAG[-/C]ATACTTGACTAAGGA | 9474 |
rs749379505 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213892 | TTCATTCCTCTCTTG[A/C]ACCATTGTGAAACGT | 9474 |
rs749383645 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227524 | TCGCTTGAGCCCAGG[A/T]GTTGGAGGCTGCAGT | 9474 |
rs749452996 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207630 | GTTAACCAATATTAA[C/T]ATTAACGTTGATAAA | 9474 |
rs749460029 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225292 | TACTGATGCATGTCA[A/G]AGATTCAATTCATTC | 9474 |
rs749561188 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195153 | CCACAAGAACAATGA[A/C]CTAAAGCACGTATTC | 9474 |
rs749564325 | in-del | -/GCTGGAGT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322964 | CGCTCTGTCGCCCAG[-/GCTGGAGT]GCTGGAGTGCAGTGG | 9474 |
rs749566840 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255653 | ATTTCAAATGTATTT[C/T]TAAGCCAGGTAATAA | 9474 |
rs749573415 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267863 | TAAAAAGACTTAAAT[C/G]TCAAGCCCAAAACCA | 9474 |
rs749573585 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237256 | AGGAAAGAAAGTTGG[G/T]CTGTATTTCTTTAAT | 9474 |
rs749599578 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312391 | AGTTTCTAACATACA[C/T]AGTTTGAGCTCCTAT | 9474 |
rs749618973 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235372 | ACGCACCCCTCCCGA[A/G]GAAATCTCAACTGCA | 9474 |
rs749632054 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263825 | CCCACAAAAAAACTC[C/T]ATCCAAAGGTCATTA | 9474 |
rs749652347 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187383 | TATTCCAAATTAAAC[-/TT]AAGATTTTGTGTTTT | 9474 |
rs749657252 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220144 | ATGCTAGATTATATT[C/T]CTAAGCTGAGAATTA | 9474 |
rs749680966 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252029 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 9474 |
rs749682741 | snp | A/G | 1.71746e-05 | 0.00293036 | intron-variant | ATG5 | GRCh38.p7 | 6:106186724 | AGTCAAAACAGTTGA[A/G]GAAAAAATAATCTGG | 9474 |
rs749702453 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247505 | TAGTAAATTCTTGTG[A/C]TTTGCAGTAGTTCTG | 9474 |
rs749706552 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221345 | CTCTATTTTCAACAG[C/T]TATAACATTTTAAGC | 9474 |
rs749726680 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245981 | TGGTCAAGGCCATGG[C/T]TGAAGACTGAATACC | 9474 |
rs749734336 | snp | C/T | 1.65864e-05 | 0.00287974 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186625 | CACTGCAGAGGTGTT[C/T]CCAACATTGGCTCAA | 9474 |
rs749760627 | in-del | -/T | 1.65021e-05 | 0.00287241 | intron-variant | ATG5 | GRCh38.p7 | 6:106201953 | AAAGAAATGTTTTAA[-/T]TGTTGCTGATTGTAT | 9474 |
rs749768574 | in-del | -/T | 5.32373e-05 | 0.00515905 | intron-variant | ATG5 | GRCh38.p7 | 6:106308335 | CTAGTATATACTTAA[-/T]GCTTAATAATGCAGA | 9474 |
rs749777521 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309530 | TATGCATTCAACAGA[-/AT]ATAAGTTATTCTTTT | 9474 |
rs749781045 | in-del | -/GTCC | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186297 | AGAAGACCTTCAGTG[-/GTCC]GTCCGGTAAGTCTTT | 9474 |
rs749785518 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189806 | TCACTACAAAGAAAA[C/T]GACTCAGGAGAAAAA | 9474 |
rs749806837 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292226 | GTGATCAACTAATAT[A/G]AGAGACCGACATGGT | 9474 |
rs749829516 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311485 | GTAGGTATGGGAGAT[A/T]CCTCTGCCTTTTCCA | 9474 |
rs749834101 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323521 | TGGTATTACAAGCAT[A/G]AGCCATCACGCCCGG | 9474 |
rs749857548 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278022 | CAATCATGGCTCACT[A/G]TAACCTTGAACTCCT | 9474 |
rs749872653 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277952 | TAAATTTTATTAATT[-/A]TTTTTTTTTAGAGAC | 9474 |
rs749893212 | snp | C/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326315 | GCGCGGTGGCTCACG[C/G]CTGTAATCCCAGCAC | 9474 |
rs749894474 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200357 | CAGAATACATTCGTA[A/T]GAAACAAGCATTATC | 9474 |
rs749900518 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216960 | TCAAGTAAGCTGTTA[-/T]TAAAAAAAAAAAAGT | 9474 |
rs749939644 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241203 | ACAAAAATACCCAAA[A/C]CCAATTCAAAAATGG | 9474 |
rs749961408 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214286 | AGCTTTACAGTAAAC[A/G]GTCTTTTGGTGGTAG | 9474 |
rs749984913 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306631 | ACTGAAAAGCCCCGC[-/T]TAGTCACACAAAATT | 9474 |
rs750029477 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254727 | CTCAGATTCAACAAG[A/C]GAAGGCACTGAGCTT | 9474 |
rs750044291 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224717 | CCTGTCTCCCCTGTC[C/T]GTACTAATACAAAAT | 9474 |
rs750048273 | snp | A/G | 7.00292e-05 | 0.0059169 | intron-variant | ATG5 | GRCh38.p7 | 6:106293152 | TAAATATTTAAAGTT[A/G]TAACTACAAGGCCAA | 9474 |
rs750056505 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252409 | GGTCATCCATTTTTC[-/CT]CTCTCTCTCTGCTGA | 9474 |
rs750070769 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262177 | CCCAGGTTCAAGTGA[-/T]TTCTCCTGCCTCAGC | 9474 |
rs750074761 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315247 | AAAGTGAAACAGAAG[A/C]AGCATTTCCTCATCA | 9474 |
rs750095786 | in-del | -/AGA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224498 | ACTGGACACTGAAAC[-/AGA]AGAAGTAGATTATGT | 9474 |
rs750097313 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213523 | TCAAGCTTCCAGCTT[C/G]AAATACATATTTTTT | 9474 |
rs750148962 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269370 | CTTCACCGGGGCTGC[-/T]GGTGGAGCTGCCTGC | 9474 |
rs750166238 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267373 | AACATTCCATGCTCA[C/T]GGATAGGAAGAATCA | 9474 |
rs750190068 | in-del | -/TACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312623 | TCTGGCAAAAAAGAC[-/TACA]CACACACACACACAC | 9474 |
rs750206416 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263334 | TGAAGGAAAGGTAAT[A/G]GCCCCACTCATGGGC | 9474 |
rs750206586 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309234 | GGCTGCTTTTATAAC[C/T]GCATCATCTTTCATG | 9474 |
rs750210104 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262635 | AGGCGGCAGGTGATT[C/T]CTGCATTTCCAACTG | 9474 |
rs750221928 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228868 | ACCCTTCTGGGTTGG[A/G]AACCTTGGTCTGCCT | 9474 |
rs750273658 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230350 | GATGGAGCAGCTGGG[C/T]TGTTATGAAATACTC | 9474 |
rs750310003 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214121 | TCAACTGTCCCATGC[A/G]TATTTGGCTTAAGAT | 9474 |
rs750320850 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321934 | AAAAATATATAAATA[C/T]ATGAATCTAGCTACT | 9474 |
rs750338856 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239164 | ATGCAATAAAGCAAG[-/A]AAAAAAAAAGTTTGT | 9474 |
rs750350218 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106201993 | GATCAATAGCAGAAG[A/G]ACAAACTTCTTTGAG | 9474 |
rs750362577 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189334 | AACAGGCCAGGTGTG[A/G]TGGCTCATGTCTGTA | 9474 |
rs750417713 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188216 | CCCTCAGCTATCTGG[A/C]ATGATTCATTGCTTA | 9474 |
rs750429366 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276863 | GAAACAAGGCACTAC[A/G]CCTTCTTAAGGAGGT | 9474 |
rs750433427 | in-del | -/TCCAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311169 | ATACTAGAATTCTGT[-/TCCAC]TCCAATGTGTAAAGC | 9474 |
rs750439174 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259001 | GAAAGGCATTGTGAT[A/C]ATCAATTGAAAATAT | 9474 |
rs750456312 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308178 | TCCAGTCATCCATGC[A/G]TCCAAACAGAAGGCA | 9474 |
rs750460736 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274913 | GATAAAATACAAGAG[-/A]AAAAAAATGCCTAAA | 9474 |
rs750482905 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272478 | TCTCAGAACTTAGTA[A/G]GCTCTTTGCTTCTGA | 9474 |
rs750497265 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189384 | TCAAGGTGGGAGGAT[A/C]GCTTGAGCCCAGGAA | 9474 |
rs750510757 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309103 | GACAAGTAGATAAAA[G/T]AAGGAGCTTGGCAAA | 9474 |
rs750528064 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228474 | TTCTCTTCTGTGACC[C/T]GTGGCTTCTAATAGA | 9474 |
rs750535027 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192077 | AATTAAATGACATTA[A/T]GAAAAATTCTTAAGT | 9474 |
rs750557418 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240513 | GTGTGAGAGAATTAT[C/T]AGTTAAAGTAAAAAT | 9474 |
rs750621414 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198667 | CTGTAATCCCAGCTA[C/T]TAGGGAGGCTGAGTC | 9474 |
rs750637806 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318381 | TTTCTCCCTTCCACA[C/T]GTCACGAACAGTAAA | 9474 |
rs750666966 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271290 | ATCCCCCTATAATTC[A/G]TGTTGAAATCCTAAC | 9474 |
rs750685194 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194180 | ATATCTAAAGAATTA[C/T]TGAAATTGTAAAACC | 9474 |
rs750699600 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319839 | GGTGCTCAAAAAATG[C/T]TTACTGAATTTGAAT | 9474 |
rs750728763 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287975 | TGGACCACAATTAAC[G/T]TTTTTTTTTTTTTTT | 9474 |
rs750751752 | snp | C/T | 3.51191e-05 | 0.00419027 | intron-variant | ATG5 | GRCh38.p7 | 6:106248287 | AAAAATGAACAACAT[C/T]ATAATGGAATACCTC | 9474 |
rs750768703 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210437 | AAAAGTATAAAAATG[-/A]AATGTAGTCTAAGTA | 9474 |
rs750800741 | in-del | -/TCTC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235780 | TTTGTATGGGAGCTC[-/TCTC]TGTCTTCACTCTATT | 9474 |
rs750831152 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234999 | TTATGTTATTTTAGC[A/G]GAAGAATGTTGTTAT | 9474 |
rs750833992 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322105 | TTGGAAATAAAGAAA[C/T]TCCAACCTGTGACGC | 9474 |
rs750853000 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297954 | AACAGAGGGAGACCC[A/T]GTCAAAATCTATTTT | 9474 |
rs750864126 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248414 | CATAAAGCAAATATA[A/T]AATTAATTTTTTTCT | 9474 |
rs750903106 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212914 | TCAAGTAGCTGCTAG[C/T]TGAGTAATAGTGGTA | 9474 |
rs750952814 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205962 | ATACAGTACCTTTAA[A/C]AACGTAATATTCTTA | 9474 |
rs750978242 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204634 | TGTTGTTCTCGTGAT[A/T]CTGAGTGAATTCTCA | 9474 |
rs751021671 | in-del | -/AAAAGCAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287919 | GGTGGCAAAATGTTA[-/AAAAGCAG]CAAATCCAAGTGAAA | 9474 |
rs751028083 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276984 | ACCTAGTTGAGAAAT[A/G]CCAGATGTATAAATA | 9474 |
rs751067414 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230425 | AATGTTGGGCACGCT[A/G]GTAAAGGACCACTAG | 9474 |
rs751072722 | snp | A/C | 1.66272e-05 | 0.00288328 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186501 | TGCTCTGATAAATCC[A/C]ATTTAAGGATGATTC | 9474 |
rs751082927 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278702 | TTACATCTCTCTTGG[C/T]CAATTCCCTTTTTTC | 9474 |
rs751158339 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231598 | GAAGAAAATCCTACC[A/G]CCTTTCTGGAGTGAC | 9474 |
rs751171286 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214399 | AGAGTTGAAAATAAG[C/G]ACTTTCTGTACTTAT | 9474 |
rs751179766 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216064 | ACTCCTTCATACCCA[C/G]TAAGACTGCTGTAAT | 9474 |
rs751181226 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324862 | CAAGTATCCAGTTTC[A/C]AGGTCTCAGAAATTT | 9474 |
rs751193053 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291543 | CACAGAAGGATCTCC[A/G]TATTTGTTGAATGAA | 9474 |
rs751193138 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243784 | TTCAGTGAGCCGAGA[C/T]TGCACTAGTGCACTC | 9474 |
rs751210580 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202587 | TTCTTAGGTACAATA[A/G]GGACAATCCTTATTT | 9474 |
rs751267188 | in-del | -/CAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272445 | ACTCTCGATCTTGAT[-/CAC]CACATTCTAGTCAGT | 9474 |
rs751271812 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291857 | TCTGTACTGTTCTTT[A/G]GTAACTAACGTGTTT | 9474 |
rs751336627 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | ATG5 | GRCh38.p7 | 6:106316093 | TTTGCCACAATCAAT[A/G]TACTTACATAGTATG | 9474 |
rs751347095 | in-del | -/TATTC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297680 | TATACACTATTCCTT[-/TATTC]TAAATTCTCTAAATT | 9474 |
rs751349351 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252519 | TAAAATGCATAAGAT[A/G]CCAAGTTAATTTGTA | 9474 |
rs751350864 | in-del | -/AATGGTAAGTATAATAGTGTTT | 1.83283e-05 | 0.00302718 | intron-variant | ATG5 | GRCh38.p7 | 6:106279871 | ATACACACATTACAA[-/AATGGTAAGTATAATAGTGTTT]AATTAACCTCTTAAA | 9474 |
rs751358942 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226757 | ATTCCCAAACAGAAA[C/T]AGAAATTATAGAGAT | 9474 |
rs751362684 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285786 | CTGTATTTCATGCAA[G/T]TTTCACGTCACAAAA | 9474 |
rs751401645 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286958 | TAACCTAGGCAGAAG[A/G]TCCAGGTATAAGCTA | 9474 |
rs751403070 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202442 | CAAAGCAAATACAAA[A/T]CATAAACCATGGCTG | 9474 |
rs751405303 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220868 | CAATAATCACCCTAA[C/G]GGGCATCATTCTGGA | 9474 |
rs751474545 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190426 | TCACCTCCCAACACT[A/G]CTGCATTGGGGATTA | 9474 |
rs751496490 | in-del | -/AATAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306094 | CCATAAAGATACTTG[-/AATAT]AATTACTTTCACATA | 9474 |
rs751498642 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324328 | GAGTTGAACTAAAGA[C/T]AGGAGGATGTGCATA | 9474 |
rs751503974 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201275 | GTATTCAAGTGTATA[-/TG]TGTGTGTGTGTGTGT | 9474 |
rs751563519 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263438 | GATTTAATCATTCCT[C/G]CCTGCTGACTCTGAA | 9474 |
rs751571294 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248585 | GGTACTACTTCTAAT[C/T]GCTGAGCTACAAAGG | 9474 |
rs751593147 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269754 | CTGGCCCGCAAGCGC[C/T]GCGCACATCCCCGGT | 9474 |
rs751633112 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206152 | AGGTGAAGCCTTTGA[C/G]AGGTAATTAGGTCAT | 9474 |
rs751653699 | snp | C/T | 1.68454e-05 | 0.00290214 | intron-variant | ATG5 | GRCh38.p7 | 6:106186695 | TTCCAAGAAAGAAAC[C/T]CAACAACAATAAAAG | 9474 |
rs751695582 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249892 | TGTGCTCAATGGCCA[G/T]TTGTGCATCTTTGCA | 9474 |
rs751712103 | in-del | -/TAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289454 | AGGCCAGGATAAGAA[-/TAAG]TAAGAACAGCTGAAA | 9474 |
rs751728572 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319883 | AGTGTATGAATATAA[A/T]ACTACAGAACCAAAC | 9474 |
rs751732753 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218456 | TAAAGCAACAAAACT[A/G]TTCAATTGTATGTGA | 9474 |
rs751752295 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187458 | TAAAGATTTTTGTCA[C/T]AGAAAAACAAAGAAA | 9474 |
rs751753615 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186226 | GAAATACAAATCGAG[A/T]GGCACATACTTCCAT | 9474 |
rs751756438 | snp | A/C | | | intron-variant, splice-acceptor-variant | ATG5 | GRCh38.p7 | 6:106217602 | CCACACTGCTGTGAC[A/C]TGAATGGGGAAGAGA | 9474 |
rs751817454 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246098 | CTAAAACTTTAATTA[A/C]ATTCAAATAAAAACC | 9474 |
rs751826477 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303786 | CATCTATTATAGCAA[C/T]CAGCTAAGGAAGAAA | 9474 |
rs751862137 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236359 | GAGCTGTTAGAACTG[C/T]TGGATCAGAAAGTAA | 9474 |
rs751890342 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256515 | AAAACATAGTCATGC[C/T]TCATTTAACGATGAG | 9474 |
rs751894276 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274192 | AATCACTAGCTTATA[A/G]GAAAAACAACTTGAT | 9474 |
rs751910297 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316599 | ACCTAAAGAGGAGCT[G/T]CACCTATACCCTGTG | 9474 |
rs751917864 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224877 | AAAGAGCGAAACTCT[A/T]GTCTCAAAAAACAAA | 9474 |
rs751919481 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283577 | CTCCCAGGAGGTCAC[C/T]GTATTGATGCTGAAC | 9474 |
rs751948014 | snp | A/G | 1.91079e-05 | 0.00309088 | intron-variant | ATG5 | GRCh38.p7 | 6:106279610 | CACAGGGTTATGGCT[A/G]TATCATATTTTATAA | 9474 |
rs751968507 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226060 | CTGAGGCTCTGTACA[A/C]GAAGAAAGTAAAATC | 9474 |
rs751970665 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213624 | AAATCAGTGGATAAG[C/G]AGAGAAAAGTGGACT | 9474 |
rs751971385 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268951 | CTTAAAACATAGATG[A/G]CGGGTTGATAGGTGC | 9474 |
rs752048641 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235132 | CCTCAGCCAATGGAT[G/T]CCCTGGATTCTCCCC | 9474 |
rs752084082 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318571 | AACTAGTGAAAGATA[A/T]ATTGGTACTTTATTT | 9474 |
rs752106465 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327526 | CACAACATGGCAAGA[C/T]CACATCTCTACAAAA | 9474 |
rs752106572 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226397 | TCAACAACAACAAAA[-/T]TACAAAGACATGCAA | 9474 |
rs752114314 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283875 | TTTCATTGAATTTGT[A/C]CATCTGTCAAATTTA | 9474 |
rs752115314 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279965 | CCAAAATACTTTAAA[A/G]TTTAACTTAAAAATC | 9474 |
rs752125396 | in-del | -/TGTCTGG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198770 | GACAGAGCGAGACCC[-/TGTCTGG]GAAAAAAAAAAGAGA | 9474 |
rs752131508 | in-del | -/AACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315663 | TATAAAAACACTTTT[-/AACA]AACAGTTGCTTAGAA | 9474 |
rs752138990 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313116 | TCAGATACCACCAGC[C/T]TCCTGAGAAGGCAGA | 9474 |
rs752143479 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194253 | TGTGGCATGAGTTTG[A/C]AAACTGAGTGCCTAT | 9474 |
rs752169300 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295086 | CACACACATATACAC[A/G]CATATATAGTACTAT | 9474 |
rs752216147 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263568 | CTGACTGGGAGAGAC[C/T]TCCCAACAGGGGTCA | 9474 |
rs752219418 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191821 | AAAAGTAAAGAGCGA[C/T]TGTAATTCTCTTCCT | 9474 |
rs752247579 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232536 | GAGCAAAGAATGCCC[A/G]TCCTGTTCAAGTTAA | 9474 |
rs752271283 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261482 | TGCTGGAATAGATGA[G/T]AAACTTCATAAATGG | 9474 |
rs752304760 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221765 | TGTTTACTATATCTA[C/G]TTATATTCCCAAAGA | 9474 |
rs752314396 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201495 | CAGGTCAAGTTTTTG[A/G]ACGAACTTGTAGATT | 9474 |
rs752318557 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323141 | ACGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 9474 |
rs752328915 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204437 | TGATTTAATTCACTT[A/C]ACTATTTGAACTCTT | 9474 |
rs752334395 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246921 | CAAATGCCGGGCACT[C/T]TTCTAGAACCTGGAC | 9474 |
rs752337443 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231741 | CTTCAAAAGTCTGCC[G/T]TAGGCCCGGAACAAA | 9474 |
rs752369146 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321032 | AGGGATAAAGAACAA[C/G]GGCAGGGAAGATTTA | 9474 |
rs752373784 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324391 | AGGGACTTGAGCATT[A/T]GAGGACTTTGGTATC | 9474 |
rs752375461 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190533 | CTCTCTACTCTCTTT[G/T]AATCTGCAACCGTTT | 9474 |
rs752380315 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203512 | CTCTCTCCCTCTTAA[C/T]GGTTATTTCACTTTA | 9474 |
rs752410810 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322927 | TCCTATCATTTATTT[G/T]ATTTTATTTTGAGAC | 9474 |
rs752449132 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278843 | CCAATCACTGACAGA[A/C]ATGGAAAGAAGTGAC | 9474 |
rs752467751 | snp | A/C | 3.31961e-05 | 0.00407394 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186522 | AGGATGATTCTGTTC[A/C]GGCAAATAGTTGATC | 9474 |
rs752472299 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240812 | GATAGTGAATACTGA[A/G]CAAATTACAGTGCAT | 9474 |
rs752473495 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198719 | AGGTGGAGGTTGCAG[C/T]TAGCCAAGATTGCAC | 9474 |
rs752482019 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319151 | TAGATACAAGAATTA[A/C]ATGAATACATGTAAA | 9474 |
rs752534589 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210814 | GTGAAGGTTATACAA[C/T]TAATTCATATAAAGT | 9474 |
rs752565183 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197480 | TCGTGTTGAAATTTT[A/G]TCACCAAAGTTGGAA | 9474 |
rs752568191 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253396 | TTGGCAGAAGGTTTC[C/T]ACCCAGGGAAATCTG | 9474 |
rs752601661 | in-del | -/A | 1.73834e-05 | 0.00294812 | intron-variant | ATG5 | GRCh38.p7 | 6:106279834 | AAACTCTATCAAAGG[-/A]AAAAATATACATATA | 9474 |
rs752612830 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316116 | ATAGTATGGTTCTGC[C/T]TCCCTTTCAGTTATC | 9474 |
rs752638298 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223372 | GAAGGGGAAAAACAT[A/G]TCTGCCAAATAAGCT | 9474 |
rs752650486 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316524 | ATTTAAGTACTGAAC[-/CA]CAGTCAAAATGAAAC | 9474 |
rs752659287 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318277 | ACCAAAACATCATGC[A/G]TGTGAGTGTGGCTCC | 9474 |
rs752731856 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284118 | TATTATGAACATTCA[C/T]GTATAAGCTTTTGTG | 9474 |
rs752761565 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292790 | ACTCGTAAATTTTAA[A/G]AAGTGTATTCAGCAC | 9474 |
rs752779737 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202033 | TAGTGTGTGCAACTG[C/T]CCATCTGCAGCCACA | 9474 |
rs752807697 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231153 | TCGGCCCAGCCAGAG[C/T]GCACGTACCTTTTTC | 9474 |
rs752832485 | in-del | -/TCAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246392 | CTCTCTCTCTCTCTC[-/TCAC]ACACACACACACACA | 9474 |
rs752851023 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310542 | TTTCATTGGTTTAAG[A/T]TCTTTTTTTTTCAAT | 9474 |
rs752884418 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209056 | GCGCATGTGGAAAAA[C/T]AGTCCTTCACACACT | 9474 |
rs752893372 | in-del | -/ACACAT/ACAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297765 | CACACACACACACAC[-/ACACAT/ACAT]ATATATATTTTAAAG | 9474 |
rs752897758 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249987 | TTCTTTATAAATTCT[G/T]AATACAAACCCCTTA | 9474 |
rs752910617 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297828 | GTAATCCTAGCACTA[C/T]GGAAGGCTGAGGCAG | 9474 |
rs752914226 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209773 | TTAGAATTGGGGGAA[A/T]CTAGATGAAGGGTAT | 9474 |
rs752960846 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269589 | GAGAAATCGAGTGCA[A/G]CGCCGGTGGGCCGTC | 9474 |
rs752981881 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218644 | CTCTACCCTGTTTTA[C/T]ATGAAGCATCCGCAG | 9474 |
rs752986117 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257547 | ACTGAAACATCATAA[C/T]GCAGAGCATGATTGT | 9474 |
rs753005409 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202645 | GGAAAGAAGTGCCAT[C/G]ATATCCAAAACTTAA | 9474 |
rs753061259 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306762 | TTTCCCCGTCCATCC[A/T]GTCATTCTACTCTTC | 9474 |
rs753061419 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292094 | CTCTCCAATAATGTA[C/T]TGGAGAGAGGCCAAG | 9474 |
rs753066452 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228668 | AAGGGACCTGAACCC[-/TT]GCAACCATGAAGGGA | 9474 |
rs753116278 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292877 | GAAAAAATTGAAAAG[C/T]ATCTTATAGACAAAT | 9474 |
rs753139971 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258455 | AGCTGTTGGTTCTCA[C/T]TACAGTGGGACCAGT | 9474 |
rs753145641 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227324 | TCTGGGACCTGGAAT[A/G]CTGGTGGACACCTGT | 9474 |
rs753194768 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318099 | ATATTGTCACTATTG[A/G]TATTATTTTTCTTCT | 9474 |
rs753203894 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214554 | ATACTATGATTAAAT[A/G]AAAGCATCCATCAGA | 9474 |
rs753214788 | snp | C/T | 3.3123e-05 | 0.00406945 | intron-variant | ATG5 | GRCh38.p7 | 6:106293002 | GTATCACAAATGGGA[C/T]GAAGGAGAAATGCAA | 9474 |
rs753246278 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316902 | TGAACACCTTTCTCT[A/G]TATCCTACTATTCCC | 9474 |
rs753255773 | snp | C/T | 3.35852e-05 | 0.00409774 | intron-variant | ATG5 | GRCh38.p7 | 6:106293129 | TGAAACAGTATATTT[C/T]GAGAAAATAAATATT | 9474 |
rs753255775 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211197 | TAAAAGGAGATTCTA[C/T]TCACTGAAACAAAGT | 9474 |
rs753274896 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195931 | CTTTTAAAAGAACAG[C/G]TTCACAAATTTGTGT | 9474 |
rs753294063 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229540 | GGAGTCAGAGAAAGA[A/C]AGACAAAGATAGAAA | 9474 |
rs753294476 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305602 | ATTTCCTTTCCTACC[C/T]GAACTTATTTAAAAC | 9474 |
rs753317456 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254406 | AGCCCTAGAAAGTTC[G/T]ACGTACTTCAGCCCT | 9474 |
rs753346326 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287511 | AAATGTGAGCTCTTA[-/C]CCTTAATCATTGCTG | 9474 |
rs753364612 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253516 | GACATTTACTCCTTT[A/T]CCCTACAAAGTAAGT | 9474 |
rs753377610 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266230 | ACACCTCTATGTAAA[C/T]AAACTAGACATTCTA | 9474 |
rs753417851 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284059 | TACATACAGTATTTT[C/G]TTTATTCATCAGCTG | 9474 |
rs753453070 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212109 | TTGCCTAACTATATA[A/G]GTAGTACTATGTGTT | 9474 |
rs753486190 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313403 | GATACATAAACGGAT[C/T]GCTGCCTAATGTTAA | 9474 |
rs753515248 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192410 | AGGTCTTATTCAACT[A/T]AGCCAATTTCAACAA | 9474 |
rs753526148 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325668 | GGACTCCAGGAAGCC[C/T]GCGCAGCCGCAAAAA | 9474 |
rs753537475 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259444 | CATTTACAGCTCAGA[C/T]ATCTGAATTGCATTA | 9474 |
rs753585749 | snp | A/C | 1.67256e-05 | 0.0028918 | intron-variant | ATG5 | GRCh38.p7 | 6:106186685 | TCCCCATCTATTCCA[A/C]GAAAGAAACCCAACA | 9474 |
rs753595948 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269393 | CTGCCTGCCAGTCCC[C/G]CGCCGTGCCCCGCAC | 9474 |
rs753596641 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265061 | CAAACTGGATAAAGC[A/G]TCAAGACCCATCAGT | 9474 |
rs753598984 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187670 | ATAAAGGAGAAATAC[A/C]CTACGTTTTCCTTTC | 9474 |
rs753600716 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266836 | TCAATAAGCTAGGTA[C/T]TGATGGAACATATCT | 9474 |
rs753622794 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321859 | ATAAGTACCTTCTTA[C/T]CACCAATATTAGTAC | 9474 |
rs753639856 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274304 | TAACTTTATTTCACA[A/G]AGAGGTTAAATATTT | 9474 |
rs753661056 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243366 | TTCTTCCAAAGACAA[C/G]TAGGAAATACAAAAA | 9474 |
rs753689556 | in-del | -/TACACACACACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312623 | TCTGGCAAAAAAGAC[-/TACACACACACA]CACACACACACACAC | 9474 |
rs753693017 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288936 | CTACTGATCCAAATG[-/TG]TGTGTGTGTGTGTGG | 9474 |
rs753711868 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261624 | ACAAGTGGTCACTGC[G/T]ACTTTAAATGAGAAG | 9474 |
rs753714087 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218628 | GATCCTTTGAAAGCC[A/G]CTCTACCCTGTTTTA | 9474 |
rs753716779 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241939 | CACACACACACTACC[A/C]CCACCACCATGATGG | 9474 |
rs753762207 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243216 | TAAAATATTAATGGC[A/G]CTTTAATGATACAAA | 9474 |
rs753780572 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306818 | CACTTCCTTTAAGTC[A/G]CCTTCCCATTCCAAA | 9474 |
rs753786147 | in-del | -/AGAAAAAGAAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251692 | GAGAGAAAGAAAGAC[-/AGAAAAAGAAAG]AGAAAAAGAAAGAAA | 9474 |
rs753799953 | snp | G/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326516 | CGGGAGGTGGAGCTT[G/T]CAGTGAGCCAAGATA | 9474 |
rs753810203 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200307 | CATGAACTGTGTGGT[A/G]TATGTCATGCAAGTA | 9474 |
rs753834440 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270080 | AGAAGGCTATAGTCC[A/G]AATTATTACAAAGTT | 9474 |
rs753849355 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320234 | CATCCATTATGTCCA[C/T]GGTATAATTAAATGT | 9474 |
rs753861489 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198891 | TGTATCCAGAATATA[C/T]AAATAATGCTAAAAA | 9474 |
rs753872898 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290202 | TGGCTTATTTTATTT[C/T]ATTTTATTTTATTTA | 9474 |
rs753888904 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318156 | CCAAGACAATTGCTC[C/T]TCCCTCCTCTTCAAG | 9474 |
rs753926115 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286866 | TCTGCCAGCAAACTA[A/G]GTCTACAAGTGGATT | 9474 |
rs753939532 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257645 | CATTTCCTCATTTGC[A/C]AAGATGGTAATATTT | 9474 |
rs753955927 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238873 | AAAGGGAAGGTCAAC[A/G]TTATGGAATGAAAAC | 9474 |
rs754013730 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227457 | AAAGATTGGCTGAAT[A/G]TGGTGGTGTGGACCT | 9474 |
rs754018607 | snp | G/T | 3.32469e-05 | 0.00407705 | intron-variant | ATG5 | GRCh38.p7 | 6:106202138 | TAAGTCTTTGTTGCT[G/T]CCAATTACAAATTTA | 9474 |
rs754022395 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209284 | CCCAGGGCTACCCAT[C/T]AAAACAGGTGAATGC | 9474 |
rs754032478 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239846 | TTCATGTTACAGAAT[-/CA]CACAGTTTCAACAGA | 9474 |
rs754054418 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236827 | TTATATGCCCCATGA[A/G]AGCAAACACAGTGCT | 9474 |
rs754093200 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324695 | ACTTTCCCCCAATTT[C/T]AAGTAGCATATCTTT | 9474 |
rs754271509 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280158 | CAGAAATGTAAAATA[A/G]TATAACCACTTTGGA | 9474 |
rs754276787 | in-del | -/TTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282402 | TTTACTAGGTTCCTG[-/TTTT]TTTATCAGTGTAAGT | 9474 |
rs754277925 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258569 | CACAACTTACTGATA[C/T]AGCTCTCCTCATTGT | 9474 |
rs754285515 | in-del | -/ATC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275464 | GTAAGCTTATTCATA[-/ATC]ATCACAAATAAAACC | 9474 |
rs754292340 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192396 | CCAATCTGGGTTTTA[G/T]GTCTTATTCAACTAA | 9474 |
rs754318152 | in-del | -/ACACACACAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297758 | CACACACACACACAC[-/ACACACACAT]ATATATTTTAAAGTT | 9474 |
rs754351203 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228358 | CCAGTGAGACGCCCA[C/T]TGCCGATCCCGACTG | 9474 |
rs754390882 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184648 | GGTACAATAATGAAT[A/G]AGGAAGTAAAAATGG | 9474 |
rs754413565 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278140 | GTGATGAGGTCTTGC[C/T]ATGTTGCCCAGGCTG | 9474 |
rs754416781 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262799 | GAAGCCATGAGGTAC[G/T]GTGCTACCCGGCTGG | 9474 |
rs754443207 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249911 | TGCATCTTTGCAGAA[A/C]TGCCTATCAAATCAC | 9474 |
rs754460889 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189391 | GGGAGGATCGCTTGA[A/G]CCCAGGAATTTGAGA | 9474 |
rs754472436 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190435 | AACACTGCTGCATTG[A/G]GGATTAAGCTTCTAA | 9474 |
rs754479958 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196760 | AAAGTTCTACAGTTA[C/T]ACAATTCTTTAAAGA | 9474 |
rs754485642 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284226 | CTGCTGTGTAATGTG[C/G]TAAGTATATCATTTG | 9474 |
rs754503455 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194302 | ATCACACTGACAAAT[-/G]TGATTATTGCTCAAA | 9474 |
rs754524436 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318724 | ACTCTGCAAAACAGA[C/T]TTATGAAAACTGCAA | 9474 |
rs754551044 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292005 | GAGCAACCTTTGGGC[A/G]GTAACTATGAATGGA | 9474 |
rs754567801 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198594 | CCAGTCTGGCCAACA[C/T]AGTGAAACCCTGTCT | 9474 |
rs754580888 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322210 | GGGACAGAGTAGGTG[A/C]CCACCAACAACATCT | 9474 |
rs754597678 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311042 | ATATGGAATACTTAT[A/G]TTTCCAAAAAAGTTG | 9474 |
rs754676000 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243809 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTT | 9474 |
rs754676904 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276876 | ACACCTTCTTAAGGA[-/G]GTGTAAATTATTGTA | 9474 |
rs754691614 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241611 | GGATGCTTCTATATA[C/T]ATGTTTTTTGGCTGA | 9474 |
rs754700703 | snp | C/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296255 | CCATGTAGTAATTAC[C/G/T]ACATGGAGCTACTGG | 9474 |
rs754706225 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210457 | TAGTCTAAGTAAATA[C/G]TAATAATGGCAGTTA | 9474 |
rs754727303 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230613 | TAGGACTAATGCTCA[G/T]CGGAAAATGACTAGT | 9474 |
rs754736567 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197252 | TGAGGCTGGGTGCAG[G/T]AGCTCATGCCTATAA | 9474 |
rs754755492 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270407 | AATTATTCACCTTCC[A/T]GCAAAACGTACTACA | 9474 |
rs754759161 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234549 | CTCCTCCCACACGAA[C/T]AGTCTGCCTACCCTC | 9474 |
rs754789343 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196398 | CCACCAGGAGATGGA[A/G]ACCTGTGTTCTAAAC | 9474 |
rs754849416 | in-del | -/TA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219778 | CAACTAGTATAATTT[-/TA]TGTTGTTCACATAAT | 9474 |
rs754881363 | snp | C/T | 5.22307e-05 | 0.00511005 | intron-variant | ATG5 | GRCh38.p7 | 6:106308356 | ATAATGCAGAAAAAT[C/T]CACTCACCATTTCAG | 9474 |
rs754883171 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185211 | AAGAAAAGGAAGCAA[C/T]GAACAATAGTAGAAT | 9474 |
rs754894484 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306821 | TTCCTTTAAGTCGCC[C/T]TCCCATTCCAAAATC | 9474 |
rs754897787 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251821 | TGAAGGAATAACCAA[C/G]TGTCTTTCACAATGG | 9474 |
rs754915896 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299241 | TACACACATTCTCCC[A/G]TATACTTTAAATTAT | 9474 |
rs754924628 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243392 | AAAAATTAGCCAGGC[A/G]TGGCACATGCCTGTA | 9474 |
rs754967013 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249928 | GCCTATCAAATCACT[C/T]TCCCTTTTAAACCAG | 9474 |
rs754985650 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308706 | TTAAGCACAGCTTAC[C/G]ACATAAATGCCCAGA | 9474 |
rs754989969 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285805 | CACGTCACAAAATAT[G/T]TTTTTAAATTTTTTT | 9474 |
rs755010596 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209403 | AGATCTCAAGGGAGT[C/T]ATGTTATGTGAAAAA | 9474 |
rs755015597 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235151 | TGGATTCTCCCCTTC[C/T]TAGGATCTCTAGCAG | 9474 |
rs755036859 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195164 | ATGACCTAAAGCACG[C/T]ATTCATAAATACTAG | 9474 |
rs755063582 | snp | A/G | 6.75368e-05 | 0.00581066 | intron-variant | ATG5 | GRCh38.p7 | 6:106186701 | GAAAGAAACCCAACA[A/G]CAATAAAAGTCAAAA | 9474 |
rs755069985 | snp | G/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325951 | CTCTCCAAGTTCATA[G/T]CTTCTACCCTCTTCT | 9474 |
rs755077870 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194291 | GGGGCAGTGCCATCA[C/T]ACTGACAAATGTGAT | 9474 |
rs755117418 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282326 | AACATGAAATGCCAT[A/C]TTTATTGTAGTATTT | 9474 |
rs755131112 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315402 | ACAGGCAGGATGTCA[C/T]CTCTGACAGAGGCAT | 9474 |
rs755184542 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309267 | TTTTATTCAAGGTGA[C/T]ATCTTTTGACTAATA | 9474 |
rs755185815 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205347 | CTTTTCAAGAATTTG[G/T]AGCTCTCATTCATAT | 9474 |
rs755188918 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264262 | ATTGAAGATCAACTT[-/A]ACTGAAAAAAAGTAT | 9474 |
rs755199018 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205017 | TAGTGATAATTTAAA[A/G]TAGCCATCCCTCACT | 9474 |
rs755205282 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267099 | TTAGAAAACCCCATC[A/G]TCTCAGCCCAAAAAC | 9474 |
rs755233230 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260577 | TTACCCCTCTTTTTC[A/G]TAAGTTGCTTATTTT | 9474 |
rs755242658 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250798 | CATAAAAGTAAACTG[A/G]AAAAAGAAACATGAT | 9474 |
rs755274802 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215887 | ATTCAGAATATGTAA[A/G]GAATTTGTAAAACTT | 9474 |
rs755286293 | snp | A/G | | | utr-variant-5-prime, intron-variant | ATG5 | GRCh38.p7 | 6:106325410 | CCCGCCATCGCGGCC[A/G]GGCGGGCGCTCCTCC | 9474 |
rs755287963 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261572 | AATTCACGTGAAGTA[C/T]CCAGAACAGAACTTG | 9474 |
rs755292888 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218462 | AACAAAACTATTCAA[C/T]TGTATGTGATATGGC | 9474 |
rs755303450 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226113 | TCATTGAAGGCAATG[C/T]CCCAACATTCACACA | 9474 |
rs755309144 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256533 | ATTTAACGATGAGGA[C/T]AGATTCTGAGAAATG | 9474 |
rs755348167 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200633 | GCGCCCCGCCACCAC[A/G]CCCAGCTGATTTTTT | 9474 |
rs755356640 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214473 | AAAAATAATAATTAA[C/T]ATTTGAAAAGCTGTC | 9474 |
rs755365077 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192425 | AAGCCAATTTCAACA[A/T]GGAATATGATCTATA | 9474 |
rs755396385 | in-del | -/TC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204695 | TTTCCTGCACTCTCA[-/TC]TCTCTTTCCTGCTGG | 9474 |
rs755407222 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275693 | TGCCCCAAAAAATTG[C/T]AATAAATGCAGTTAT | 9474 |
rs755416480 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266531 | TATGATACCAAAACC[C/T]GGCAGAGACACAACA | 9474 |
rs755422658 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278150 | CTTGCTATGTTGCCC[A/C]GGCTGGTCTCCAACT | 9474 |
rs755438780 | snp | C/T | 4.97706e-05 | 0.00498827 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279783 | TGAGCTTCAATTGCA[C/T]CCTTAGATGGACAGT | 9474 |
rs755449450 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305581 | AGTTGTCTCAACTGG[C/T]GACTAATTTCCTTTC | 9474 |
rs755454894 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283924 | TTCAATTAATATAAA[C/T]GCATTATATAATGTG | 9474 |
rs755472594 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255226 | ATCGCTTAAGACCTA[C/G]ATAACCATTCCTTTC | 9474 |
rs755505776 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315585 | TAGCTCACATATAAC[A/T]TACAATAGCTCAGTG | 9474 |
rs755526670 | snp | G/T | 1.91915e-05 | 0.00309764 | intron-variant | ATG5 | GRCh38.p7 | 6:106279611 | ACAGGGTTATGGCTG[G/T]ATCATATTTTATAAA | 9474 |
rs755535932 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224921 | ACAAAACACAGAAAT[A/C]CATCAATTAAAAAAG | 9474 |
rs755559193 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316665 | CATTTACCCCTGCCC[C/T]GTCCAATATATTCAC | 9474 |
rs755604495 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194841 | GAAATGAAGTATAAT[A/T]GGGTAAAGCTTATAG | 9474 |
rs755637632 | snp | C/T | 1.71516e-05 | 0.0029284 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279822 | TCTTTTTCTGGAAAA[C/T]TCTATCAAAGGAAAA | 9474 |
rs755651773 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221776 | TCTACTTATATTCCC[A/G]AAGACATCTTAAGGA | 9474 |
rs755655020 | in-del | -/ATTA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277945 | TTATTTTTAAATTTT[-/ATTA]ATTATTTTTTTTTAG | 9474 |
rs755698361 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278855 | AGACATGGAAAGAAG[C/T]GACATAATTTATCAC | 9474 |
rs755705245 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210872 | TTCTCAATGAGTGTT[A/G]TAATTGTTCTTTTTA | 9474 |
rs755727931 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324460 | GGGACAGGAAAGACT[A/G]TACCTTAATTTTTGT | 9474 |
rs755749712 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263659 | GCTTCCAGAGGAAGT[A/G]GCAGGCAGCAATCTT | 9474 |
rs755769175 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255789 | CCATTTTCCCTTCAT[A/C]CATGACAATCTTTAA | 9474 |
rs755776150 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232604 | TACCCCCTTAGACCC[A/G]AGGCTCAACAAGGAC | 9474 |
rs755799267 | snp | A/T | 1.89928e-05 | 0.00308157 | intron-variant | ATG5 | GRCh38.p7 | 6:106279620 | TGGCTGTATCATATT[A/T]TATAAAGTGGTATTC | 9474 |
rs755808732 | in-del | -/TGT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204619 | GGGTGGTTTTCCTCA[-/TGT]TGTTCTCGTGATACT | 9474 |
rs755823374 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228598 | TTAGAAGCAGCCCGC[A/C]ACCATCTTCGGAGTT | 9474 |
rs755826128 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190543 | TCTTTTAATCTGCAA[C/T]CGTTTTTTAGCCTTT | 9474 |
rs755829192 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186157 | TTTCCACTTTCATGA[G/T]CTAAAGTTCAACCAT | 9474 |
rs755851969 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319265 | AATGTTTAAAAGTCA[A/G]CATTTAAAGACTTCA | 9474 |
rs755856590 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196667 | GGCAGGGGTTGCAGT[C/G]AGCTGAGATGGCATC | 9474 |
rs755874345 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217625 | GGAAGAGAAACGCCA[C/T]AGTAAGGGAACTCTT | 9474 |
rs755878199 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198751 | ACTGCGCTCCAACCT[A/G]GGTGACAGAGCGAGA | 9474 |
rs755916527 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229253 | AAACCCAGGGAGTCT[C/T]GTCCCTGGTGTCCCT | 9474 |
rs755972528 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270088 | ATAGTCCAAATTATT[A/G]CAAAGTTAATTTATT | 9474 |
rs755978408 | snp | A/C | 4.97748e-05 | 0.00498848 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186526 | TGATTCTGTTCAGGC[A/C]AATAGTTGATCCTTC | 9474 |
rs756019944 | snp | G/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316127 | CTGCTTCCCTTTCAG[G/T]TATCTCATCCTGATA | 9474 |
rs756046799 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211896 | TACTTTGTGTGTGTG[C/T]TTTGTTTTTAAGTCT | 9474 |
rs756047843 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287176 | TCAAGAACTTCAGGA[A/G]AGAAAAGCTACCACA | 9474 |
rs756082253 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285307 | TTTAATTCATTTTTC[C/T]GGTAGTACCAAGATG | 9474 |
rs756090936 | snp | C/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240824 | TGAACAAATTACAGT[C/G/T]CATCTACAGATTAAA | 9474 |
rs756112394 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195968 | CTTGTGTAGGGTCAC[A/G]TTAATCTTGTCTTGT | 9474 |
rs756123249 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267697 | ACCACAAATCTACAA[A/C]CATCTGATCTTCGAC | 9474 |
rs756155676 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295495 | AAATGTGTGAAACAC[-/TT]TTGTGAATTTGTAAG | 9474 |
rs756176023 | in-del | -/T | 1.65916e-05 | 0.00288019 | intron-variant | ATG5 | GRCh38.p7 | 6:106292979 | TCTACTCGAAGTCTA[-/T]TTATTATGTATCACA | 9474 |
rs756177536 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225011 | CAAGCCATCATCATT[A/G]CTGTTAAAATAACTC | 9474 |
rs756189973 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316939 | AGTATGCTCCTCTCT[C/T]ACTTATTCAAATCCC | 9474 |
rs756208183 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315774 | TTCCATTATCATACA[C/T]TTATTATATATGAAT | 9474 |
rs756221792 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236615 | ATCTTTTCATGTGCT[C/T]ATTAGCCATTCCTAT | 9474 |
rs756236799 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195134 | CAGCTCATCATTAGT[C/T]ACTCCACAAGAACAA | 9474 |
rs756327540 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313213 | AGTAAATGTGTGGGA[C/T]GCAGATAGGTTTTGC | 9474 |
rs756338571 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227046 | GAGTATCTGAAAAAA[C/T]AATGGCCCTAAACTT | 9474 |
rs756357015 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202038 | TGTGCAACTGTCCAT[C/T]TGCAGCCACAGGACG | 9474 |
rs756410326 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205715 | TTTCCCAAATCTGAG[A/C]AAGTATTATAAAGGT | 9474 |
rs756421845 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210566 | ATTTCAAATAATTTA[C/T]GGCCTGGTACAGTAA | 9474 |
rs756435593 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246932 | CACTTTTCTAGAACC[G/T]GGACACAAAGCATGA | 9474 |
rs756452550 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251354 | TAGCCTTTGCAGGTG[G/T]GACCCCTTACAAGTT | 9474 |
rs756458684 | in-del | -/ACACACACACAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297756 | CACACACACACACAC[-/ACACACACACAT]ATATATTTTAAAGTT | 9474 |
rs756475550 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215885 | CTATTCAGAATATGT[A/G]AAGAATTTGTAAAAC | 9474 |
rs756510208 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287975 | TGGACCACAATTAAC[-/T]TTTTTTTTTTTTTTT | 9474 |
rs756570202 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256622 | CAGATTACTACACAA[C/G]TAGGCTATATGGTAT | 9474 |
rs756587007 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213019 | CTTTGGTTTTACCTA[C/T]GTTTAACAAAAGCAT | 9474 |
rs756637925 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189476 | AAAGATTAGCTTTAG[C/T]TGGGCGTGGTGGTGC | 9474 |
rs756647137 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305680 | TGCTTCTCTATCCTT[A/G]AGACACTTGTATGGT | 9474 |
rs756672075 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240956 | CCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 9474 |
rs756677418 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272961 | AAACAAGGCTGGCCA[C/T]ATACTGGTAACAGAT | 9474 |
rs756700243 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274987 | TCCACTTTTCTATAA[A/T]GCTCTGTGAAGACAG | 9474 |
rs756702202 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292115 | AGAGGCCAAGGCAGG[C/T]GGATCACTTGACTTG | 9474 |
rs756775759 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239316 | GAAGAAAACCTTAAA[A/T]TCTATGCAGAACATA | 9474 |
rs756797636 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192629 | AAATATGGAGTAGAA[-/G]TCTAAGATCAAATGA | 9474 |
rs756825191 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216323 | TGCAGCTTTTATTCA[C/T]AATAGCCAAAAAGTG | 9474 |
rs756829793 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288573 | AAGCTTTTGGTTCTA[C/T]AGACAATTACCATTA | 9474 |
rs756853831 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293036 | ACTATACCTTAAAAT[A/G]TACTGTGATGTTCCA | 9474 |
rs756877852 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319357 | TAAAAATTTTGCAGT[A/T]AACACTGCTAATAAT | 9474 |
rs756898666 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253555 | CTTAGAAAATTGGCA[A/T]CAAGAACAGTAATCA | 9474 |
rs756913418 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192702 | TATAATTCAGCAGAA[A/C]ATGACTTGATTTGCT | 9474 |
rs756917742 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301751 | ATAATACAAACATTC[C/T]AAAATCTGAAAAAAT | 9474 |
rs756947085 | snp | A/G | 1.73963e-05 | 0.00294921 | intron-variant | ATG5 | GRCh38.p7 | 6:106279834 | AAACTCTATCAAAGG[A/G]AAAAATATACATATA | 9474 |
rs756947903 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261632 | TCACTGCTACTTTAA[A/G]TGAGAAGCAGTTTTA | 9474 |
rs756959738 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265119 | ATGCAAAGACACACA[C/T]AGGTTCAAAATAAAG | 9474 |
rs756982913 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206256 | CCTTCTGCCATGTTG[C/G]GGGGGTGGGGGTGGG | 9474 |
rs756986599 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194550 | TTTCTTTTTCTTTTT[-/T]TTTTTGAGATGGAGT | 9474 |
rs757011553 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218656 | TTATATGAAGCATCC[A/G]CAGCTAAAATGAACA | 9474 |
rs757012015 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230222 | TTGCACTCAGCCAAG[A/C]CTTAACGTACTTACC | 9474 |
rs757013168 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187741 | AGGTCTGGGCAAAAT[A/G]AGCTGATGATGTATG | 9474 |
rs757031848 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302836 | TTTTAAAAATACACA[A/G]ACCCGAATGAAAACA | 9474 |
rs757062934 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219724 | CGACAGATGGCTATA[C/T]ATAAATCACTCAGTG | 9474 |
rs757158272 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186548 | TGATCCTTCAATCTG[C/T]TGGCTGTGGGATGAT | 9474 |
rs757185930 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310622 | TGTACAGTTTAGTAA[C/T]ACTAAATACATTCAC | 9474 |
rs757240513 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229485 | GACAGAGAGGAGAGG[A/G]AGAGAGACAAAGAGG | 9474 |
rs757249603 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262141 | GCAGTGGCACCATCT[C/T]GACTCACTTCAACCT | 9474 |
rs757253939 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260874 | CAGAACTGGTCTATA[C/T]AGGCCAAGTTCAAGA | 9474 |
rs757261817 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236545 | TCCAATCTAGGGAAC[A/G]TGAAGTAGTATCTCA | 9474 |
rs757275867 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321885 | AGTACAGTTAGCACA[C/T]AGTAGGCTTTGAAAT | 9474 |
rs757282744 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106186769 | CCTTAGTGCATTAAA[C/T]GGATTTTAAACATGT | 9474 |
rs757295157 | in-del | -/TATATTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297769 | ACACACACACACATA[-/TATATTT]TAAAGTTCATTGGGG | 9474 |
rs757301575 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216009 | GAAAAGATGTTTAGC[A/G]TCACTGGTCATTAGG | 9474 |
rs757321575 | snp | A/G | 1.69306e-05 | 0.00290947 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308392 | TGCCTTCATATTCAA[A/G]CCATATCTCACTAAT | 9474 |
rs757323584 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214834 | GAACAAATGGTATTG[C/T]TTTTAAATTTTTATA | 9474 |
rs757328572 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200316 | TGTGGTATATGTCAT[A/G]CAAGTAATCCTGCAT | 9474 |
rs757339585 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306888 | ATTGCCTTATCTATG[A/C]TGCGTGAGGTCTAGA | 9474 |
rs757435842 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309113 | TAAAAGAAGGAGCTT[A/G]GCAAAAATTTATGGT | 9474 |
rs757475059 | snp | C/T | 1.66258e-05 | 0.00288316 | intron-variant | ATG5 | GRCh38.p7 | 6:106202139 | AAGTCTTTGTTGCTG[C/T]CAATTACAAATTTAT | 9474 |
rs757497400 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252386 | TACCATTCCTCAAAA[A/G]TCCTGATGGTCATCC | 9474 |
rs757505645 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305945 | CTGGAAGTTATTCAC[A/G]CCTCATATATATGGA | 9474 |
rs757529941 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278898 | CATCTGTTGTTATGT[-/A]ATGATTCCTGGACTA | 9474 |
rs757530716 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270263 | AAAATATATAATATA[G/T]ATAGTAAAATGCTTG | 9474 |
rs757533031 | in-del | -/TGGTAAGTATAATAGTGTTTAATT | 1.83869e-05 | 0.00303202 | intron-variant | ATG5 | GRCh38.p7 | 6:106279873 | ACACACATTACAAAA[-/TGGTAAGTATAATAGTGTTTAATT]TTAACCTCTTAAAAG | 9474 |
rs757567992 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202050 | CATCTGCAGCCACAG[A/G]ACGAAACAGCTTCTG | 9474 |
rs757568805 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233945 | TTACCTAAAGGAAAC[C/T]CCACCTTCACTGCCC | 9474 |
rs757569608 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258674 | TGATACCATGACACA[C/G]AAGATTTTTAGTTAC | 9474 |
rs757583866 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192557 | TTTAAGGGAAATTCA[C/T]ACATGTTTTTAACAA | 9474 |
rs757601430 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325676 | GGAAGCCCGCGCAGC[C/G]GCAAAAAGCACCGGC | 9474 |
rs757630525 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324743 | CTTAAATCTGGTGTA[A/G]AATACCTCTCAATTA | 9474 |
rs757637216 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190675 | ATAAAAAAAAAGTTA[C/T]GTTTTAAGAAAAACA | 9474 |
rs757651102 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221882 | CTAGCATAATAAAAA[C/T]ATGAGTGTCTTATTA | 9474 |
rs757676899 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293533 | TAAAACGCATGCAAA[C/T]CACCTATTCTGTGGT | 9474 |
rs757679929 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313499 | CAATCCAAATGAGTA[C/T]ATGTGTTTTTATACT | 9474 |
rs757705024 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201176 | TTTTCTTTCCCAAAT[A/G]TTTTTTATCTGCTGT | 9474 |
rs757753298 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308096 | AAATATATCTGAAAA[C/T]AGCCCATAACCAAAT | 9474 |
rs757755669 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246106 | TTAATTAAATTCAAA[C/T]AAAAACCAAAATGGA | 9474 |
rs757757815 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258574 | CTTACTGATATAGCT[A/C]TCCTCATTGTAGAGA | 9474 |
rs757760906 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210326 | AAAGGCAGATAATAT[A/G]TACTATAACAGAGCA | 9474 |
rs757799999 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229613 | GTAAATGTAAAACCT[A/G]TAATTGATAATTGAA | 9474 |
rs757809206 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247237 | GATTAGAGTCTAAGC[C/T]TGTGACATTATGCTT | 9474 |
rs757832291 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320924 | CAGCAACTAAGGCAA[A/G]AAGTAATGAGTGCCT | 9474 |
rs757837602 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274831 | GATACAAAAATGTAA[C/G]ATGTACCCCAACCAG | 9474 |
rs757853238 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217280 | TTTGTCTTAACTGTT[C/T]ACCAAAACTCATTTA | 9474 |
rs757867139 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200362 | TACATTCGTAAGAAA[C/T]AAGCATTATCTGTTA | 9474 |
rs757888132 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234237 | TAAAACTACATGAAA[-/C]CCTCCATACCCATAC | 9474 |
rs757894085 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201899 | ATAACCTGTTGTTTA[C/T]AAATGTGGAATGCTT | 9474 |
rs757959282 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303742 | TAAATGTATACAAGG[G/T]TGGTCCAACATCAAA | 9474 |
rs757965882 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321993 | CAAATCAGTATAGTC[A/G]CACTTTAAATTCGGC | 9474 |
rs757999926 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297719 | CAAAATGACTTAAAC[-/AC]ACACACACACACACA | 9474 |
rs758000637 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199276 | CATATTTGAATGTTC[C/T]TAGCAGCTCTGTTTA | 9474 |
rs758019391 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288728 | CAGAATCAGAAACTG[C/T]ACTTTAGTAAGAGAC | 9474 |
rs758046255 | snp | A/G | 3.56716e-05 | 0.00422309 | intron-variant | ATG5 | GRCh38.p7 | 6:106293158 | TTTAAAGTTATAACT[A/G]CAAGGCCAAAATAAA | 9474 |
rs758055134 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213527 | GCTTCCAGCTTGAAA[C/T]ACATATTTTTTTTTA | 9474 |
rs758098225 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220767 | TTATGAGAAGAACAG[A/G]AAAAAAAATTAGAAG | 9474 |
rs758115674 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213680 | AATGTCAAATGTAGT[A/G]GAAATAACAAAGGTT | 9474 |
rs758133759 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309266 | TTTTTATTCAAGGTG[A/C]TATCTTTTGACTAAT | 9474 |
rs758194349 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284259 | GACATACCAAACTGC[C/T]TTCCAAAAAGGCTAC | 9474 |
rs758217812 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208040 | GAGGTTGCAGTGAGC[C/T]GAAATCGCGCCACTG | 9474 |
rs758271284 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236864 | ACTAATGAGTATCAC[C/T]AGCACATAGAACTGT | 9474 |
rs758298863 | in-del | -/A | 1.73834e-05 | 0.00294812 | intron-variant | ATG5 | GRCh38.p7 | 6:106279833 | AAACTCTATCAAAGG[-/A]AAAAAATATACATAT | 9474 |
rs758308716 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262652 | TGCATTTCCAACTGA[C/G]GTACCCAGGTCATCT | 9474 |
rs758338833 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299195 | GATGCTTAAACCCTT[A/G]TATTAAATGGCATAG | 9474 |
rs758344157 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261917 | TGCACAGGACAGCCC[C/G]AACCCTCACAGCCAC | 9474 |
rs758349771 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260252 | CCCTAGAACTTAAAG[C/T]ATAATTTTTTAAAAA | 9474 |
rs758398177 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234884 | TGCAAGATCAACTTA[A/C]CTTCCTAGCATCAGT | 9474 |
rs758412800 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311971 | AGGTAGCTGGGATTA[C/G]AGGTGTCCACCACCA | 9474 |
rs758420926 | in-del | -/TGGGGC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286309 | CCGTTCCAAAGCACA[-/TGGGGC]TCACCTTGTTTGTTC | 9474 |
rs758425292 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298173 | TTTCTGTTGGCCAGG[C/T]TAGTCTTGAACTTCT | 9474 |
rs758446630 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247438 | GACTTAAGAGCCTAT[C/T]GCCTACTTTGTGGTA | 9474 |
rs758476883 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294921 | GTACTTTTAGTCTTA[C/T]ATGCATTATATCTCT | 9474 |
rs758489484 | in-del | -/AAGG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246203 | TGTTGCTTTCTGTTT[-/AAGG]AAAAACTGCCCAAGT | 9474 |
rs758490537 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208077 | AGCCTGGGCAACAGA[C/G]CAAGACTCTGTCTCA | 9474 |
rs758521465 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217404 | ATAAGGAGTAATATG[A/G]AATAAAAGTATCAAA | 9474 |
rs758598034 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324976 | CTCCTCACCCCTCAG[A/G]AAAATCTAGAACCAA | 9474 |
rs758644391 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301176 | GTCTGAAGAAAGAGA[-/CT]CTATTTTGAGTTAGG | 9474 |
rs758661105 | snp | C/T | 4.94434e-05 | 0.00497184 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316146 | CTCATCCTGATATAG[C/T]GTGAAACAAGTTGGA | 9474 |
rs758669463 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271520 | CTTGGACTCTCTAGC[C/T]GCTAGATTGTGAAAA | 9474 |
rs758679198 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184884 | CCCAAAATGAACCGA[C/T]GAATAAACACTCTTA | 9474 |
rs758706697 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228549 | CCATGAGGCCAAGAA[A/C]CCCAGGTCAGAGAAC | 9474 |
rs758726223 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223930 | AGGAGGTTAAATTAG[G/T]TAATTCTTCCAGCCT | 9474 |
rs758735755 | snp | A/G | 1.7648e-05 | 0.00297047 | intron-variant | ATG5 | GRCh38.p7 | 6:106248293 | GAACAACATTATAAT[A/G]GAATACCTCACATGA | 9474 |
rs758754259 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315411 | ATGTCATCTCTGACA[A/G]AGGCATAAACTGGGA | 9474 |
rs758762606 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315981 | GTTAATTTTTTTTCC[-/A]AAATAAGCATGAATT | 9474 |
rs758767769 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266438 | GGAACTGGTACCACC[A/G]TTCCTTCTGAAACTA | 9474 |
rs758775427 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224813 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9474 |
rs758811351 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280599 | ACATATAGGGAGTTA[C/G]GTAAATGAGACGACT | 9474 |
rs758827420 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248507 | AAACATATAAACATA[C/T]GACTACTTGTGTTAT | 9474 |
rs758892292 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231414 | GGAAAGAGAACGATT[C/T]CCCACAGGCCAGCAG | 9474 |
rs758892378 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192681 | TGTAGCTTCATATTT[A/G]TATTTTATAATTCAG | 9474 |
rs758902687 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294185 | GCAAAAAGAAGACTA[C/T]TTGGTGTTATACACA | 9474 |
rs758915000 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222581 | AATAAGAAGCCTGAT[A/G]TGTGTGAAAACTGGA | 9474 |
rs758933932 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325841 | CCCACGTGGTCCGAA[C/T]TCCGCCCTCCGTGTT | 9474 |
rs758965626 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282198 | ATGAGCTGTACTCAT[C/G]TACATCAGGTGCTAC | 9474 |
rs758999303 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237229 | AATAAAAGCAAAACT[-/AA]ACCCAATAAGAGGAA | 9474 |
rs759010302 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204383 | TGACAAGTATGAAAA[C/T]TGTAATTTTTAAAAA | 9474 |
rs759030880 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216687 | CTCTGTGTAACTTAG[A/C]ATTCAGTGACTCCTA | 9474 |
rs759090146 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324330 | GTTGAACTAAAGATA[C/G]GAGGATGTGCATAGG | 9474 |
rs759096052 | snp | A/C/T | 6.66306e-05 | 0.00577163 | synonymous-codon, missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186663 | AATCATCACTTGATT[A/C/T]TTTTTTTCCCCATCT | 9474 |
rs759100903 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203379 | GTACCCAGTTTCCTT[C/T]ATCTGTTAATTTGGG | 9474 |
rs759103119 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257438 | ATGCATTGTGCTATG[A/G]TGGTACAAGGGCTAT | 9474 |
rs759111628 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288199 | AGGCCTCAAACTCCT[A/G]ACCTCAAGAGATCCA | 9474 |
rs759113269 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225611 | AGTGAGGACCCTGAA[C/T]ATACTCTCCTCCATA | 9474 |
rs759120697 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215575 | CCACTTACGTAATCT[G/T]ATCAACAAATTTTAA | 9474 |
rs759128362 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247674 | GAGCACTTCAGTGCT[A/G]CATTTGGAGTCTGTT | 9474 |
rs759153101 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309845 | TCTTTTAGCAAACCT[G/T]GAACTTTAATTTAAA | 9474 |
rs759157858 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228193 | GTTTTCACTCTATTA[A/C]ATCTTGCAACTGCAC | 9474 |
rs759243800 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318789 | CAAATTTATAGGATC[C/T]TAAAATGTTAATCTT | 9474 |
rs759244600 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292815 | CAGCACTAATAAAGA[A/C]AAGCAGTTCATATAT | 9474 |
rs759279827 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224298 | AGCAGGTAGAAAAAT[C/T]TAAGAACCACTAAAA | 9474 |
rs759282780 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307624 | TCACCGCAACCTCCA[C/T]CTCCCAGGTTCAAGC | 9474 |
rs759287110 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258337 | ATGACCTTACCACTG[C/T]ATCTTAGCCTGGGTG | 9474 |
rs759309168 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184395 | TATTTCTCCAAGAAA[C/T]TTTTATGACAGTTTG | 9474 |
rs759309254 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200702 | AGCCAGGATGGTCTC[G/T]ATCTCCTGACCTCGT | 9474 |
rs759347141 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313056 | AGCAGATAAGAAGTT[G/T]AAAGTAAAATAAACA | 9474 |
rs759359642 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281723 | GTCATAGAGTAAGTG[-/T]TATGTTCTAACTTTA | 9474 |
rs759395760 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185732 | ATATTTATACGTGTA[C/G]TGTGTAAAGAACACA | 9474 |
rs759443518 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271527 | TCTCTAGCCGCTAGA[C/T]TGTGAAAATAATCAG | 9474 |
rs759445084 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191764 | ACTGATAAAGTATGT[A/G]AGGACAGAAGATCAT | 9474 |
rs759457336 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221641 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 9474 |
rs759488279 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282937 | AACCACAGGTGTACA[A/C]CACCACACTCAGCTA | 9474 |
rs759506418 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207762 | TGAGTTATATACAGT[A/T]ACATGATGCAACAAA | 9474 |
rs759508745 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219618 | TATGCATAGGTTATA[C/T]GCAAATACTACACCA | 9474 |
rs759516272 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193409 | AAACAATTTAAAAAC[A/G]TGTCCATATTAATTC | 9474 |
rs759548889 | snp | C/T | 1.68479e-05 | 0.00290236 | intron-variant | ATG5 | GRCh38.p7 | 6:106248256 | CTGTCTGTAATGATA[C/T]AAATTATTTGTTATT | 9474 |
rs759629197 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321720 | GTTTTCCCCTATGCA[A/G]CCTCTAGTCTAATTA | 9474 |
rs759644456 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262316 | TGATCCACTCACCTC[A/G]GCCTCCCAAAGTGCT | 9474 |
rs759675378 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267215 | CAAAGAAGCAGAGAG[-/T]CAAATCATGAGTGAA | 9474 |
rs759690096 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220289 | TGCACACAACAATAC[A/G]TAACTGTACTTATAT | 9474 |
rs759695653 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263055 | GGTCTCGCTCAGTGG[A/G]TCCCACTCCTACGGA | 9474 |
rs759708909 | snp | C/T | 9.96429e-05 | 0.00705773 | intron-variant | ATG5 | GRCh38.p7 | 6:106293119 | TGCCTAAAAATGAAA[C/T]AGTATATTTTGAGAA | 9474 |
rs759720656 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311615 | TACAGAGTTAAGACA[C/G]AATAGTGCTGAGGAA | 9474 |
rs759730934 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322745 | TGAAGATCTCTCACA[C/T]GGTTTTAAATAACAC | 9474 |
rs759764315 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294536 | TAGGAATTTAGGATG[G/T]GCTGGGTACTGTAAC | 9474 |
rs759809868 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322919 | CTCCTCTCTCCTATC[A/T]TTTATTTTATTTTAT | 9474 |
rs759875250 | in-del | -/CACACATA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297761 | ACACACACACACACA[-/CACACATA]TATATTTTAAAGTTC | 9474 |
rs759879868 | in-del | -/ATT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275550 | ATATTTTAACCAAAC[-/ATT]ATTAAGTTGGATTTA | 9474 |
rs759881852 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276140 | CAGATATCAATGAAG[C/T]AAACCTAACAGATAT | 9474 |
rs759915921 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226991 | GCATACCAATATACA[C/T]ATAATGAGAGGCCCA | 9474 |
rs759937046 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196744 | AAAAAAAAGTAGATT[C/G]AAAGTTCTACAGTTA | 9474 |
rs760047653 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317795 | CTCACTGAAAATAGG[A/G]AAGACCTCACTACGT | 9474 |
rs760105248 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106325875 | CCTAACCCAGCAAGG[A/G]GGCCCGAGTCGCTCT | 9474 |
rs760123917 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234846 | TGGTGACATGGAATG[G/T]GTTGCCGACTCCCTG | 9474 |
rs760145086 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236560 | GTGAAGTAGTATCTC[A/C]CTGTTATTTTCATTT | 9474 |
rs760175574 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185242 | CTCACTTCAGCATTT[A/G]TATAATTTTTTATAA | 9474 |
rs760176356 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252199 | ACTTAGCTTATTCAC[A/G]TTGGGAGGAAGATAA | 9474 |
rs760187710 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205787 | GGGGACAAAGCCCCA[A/G]TGCTATTACATAGTG | 9474 |
rs760215167 | in-del | -/AG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243013 | TTCTGGAAACAAAAC[-/AG]AGTCTAAAATTTGGC | 9474 |
rs760246770 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326788 | GCCACAGGATTCTTT[C/T]AAAAAGAAAAATCTT | 9474 |
rs760246834 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314327 | TTTGGAAGGCCGAGG[C/T]GGGCAGATCACTTAA | 9474 |
rs760275075 | snp | C/T | 1.66838e-05 | 0.00288818 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186673 | TGATTCTTTTTTTCC[C/T]CATCTATTCCAAGAA | 9474 |
rs760275195 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192252 | TGAAAACATTCAGGT[-/A]AAAAAAAAAAACCTT | 9474 |
rs760312835 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217896 | TTGAGATAATAATAA[C/T]ACCACCAATTCATCA | 9474 |
rs760314964 | snp | A/C | 1.64863e-05 | 0.00287104 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106201983 | TTACCTTCAGGATCA[A/C]TAGCAGAAGGACAAA | 9474 |
rs760345665 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244786 | GGCAAATATGTGTGT[A/C]AATAAACTTGTTGAA | 9474 |
rs760351507 | in-del | -/ATGTGTAAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208253 | TGTGTATATATACAT[-/ATGTGTAAA]CTGTGTAAACACATA | 9474 |
rs760382863 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294356 | GCTACTCTGGGCACG[A/G]TGCTTATGGGATAGC | 9474 |
rs760405075 | in-del | -/TTATT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290190 | GCCACCATACTTGGC[-/TTATT]TTATTTTATTTTATT | 9474 |
rs760416282 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290969 | CAAATACTATCACTT[-/G]GTTTTCCCTGCAGTG | 9474 |
rs760422355 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232722 | CCAGTGGACAGTGGA[A/G]GTTAGTGCAAGATCT | 9474 |
rs760431461 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247961 | CTACAAATAATGAGT[A/T]CCAAATGCATATGAG | 9474 |
rs760437882 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295652 | CACTACAATCTTGAC[C/T]TCCTGGGCTCAAGCG | 9474 |
rs760443984 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220212 | ACTTGCCTAAAGATT[G/T]CAGGAGTTTCAAGTA | 9474 |
rs760449830 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289938 | AGGCTCACAAAGATA[G/T]GTAGTTTAAAAGAAG | 9474 |
rs760464028 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230483 | GTGATCAAGAAAGGC[A/G]GGAAAAGGGGTGAGG | 9474 |
rs760474773 | in-del | -/ATGTCTGAGGCTTTCATAAATGGATGTTTTTTAAA | 5.07593e-05 | 0.00503756 | intron-variant | ATG5 | GRCh38.p7 | 6:106248101 | AGTGCTTCAATTAAG[lengthTooLong]ATGTTATTTCCTACC | 9474 |
rs760475808 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243010 | CATTTCTGGAAACAA[A/G]ACAGAGTCTAAAATT | 9474 |
rs760476449 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255848 | GCTACAGCACAGTGG[C/T]AGGCCAGGACTAATT | 9474 |
rs760482406 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200145 | TGACTAAGGAAAATT[A/G]CAATATTCTCAGGCT | 9474 |
rs760500421 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317963 | TGATACATCCAGTTA[C/G]TCAACAGCTGCAACT | 9474 |
rs760528356 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265909 | CGAAAGATCTAAAAT[C/T]GACACCCTAACATCA | 9474 |
rs760534442 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269039 | TATCCTAGAACTTAA[A/C]GTAAAATAAAATAAA | 9474 |
rs760556223 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292506 | TTCTATCTCCTAACC[A/C]TTCTCTTAATTCATT | 9474 |
rs760581545 | in-del | -/AAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209333 | AGGTCTGTCCCACGG[-/AAT]ACTACTCAGCAATAA | 9474 |
rs760582978 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213939 | ACAGTATTTAGTTGT[C/T]ACAGAACCCATTAAG | 9474 |
rs760584332 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315154 | CTCCAGTAATCTGAC[G/T]TTCCGTAGCTGGAGC | 9474 |
rs760592194 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294270 | GCAAAATTTGAAAAC[A/C]CATCAAATTTATCTC | 9474 |
rs760684452 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218022 | TTCTAAGAAAATAGT[A/T]TACATCAAATATTAA | 9474 |
rs760693614 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193932 | GTGCTAAAGATGAAA[C/T]AGTTGTGCAAGTGTG | 9474 |
rs760717290 | snp | A/T | 1.65592e-05 | 0.00287738 | intron-variant | ATG5 | GRCh38.p7 | 6:106202130 | CAAGCAATTAAGTCT[A/T]TGTTGCTGCCAATTA | 9474 |
rs760725276 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221544 | TACAAAAATTAGCTG[C/T]GCCTGGTGGTGTGCG | 9474 |
rs760742868 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192175 | TAAGTCAAATGAGCC[C/T]TAGTGTACTACAGAT | 9474 |
rs760795969 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252233 | ATATACTTCTCGCCA[A/G]AGCTACAAGCAATAT | 9474 |
rs760830043 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299100 | AAAAGCAAGTAGTAA[A/G]GATTTGAACCTGGAA | 9474 |
rs760843208 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209918 | TTCTCTGAGGACCTG[C/T]AGCATTTTGGTTATC | 9474 |
rs760850801 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253072 | AGAAAACACATTCAA[A/C]TATAGACCCATATGA | 9474 |
rs760903219 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315061 | GCCAGATGCTGAGGA[C/T]GCACAGAGGAAAACA | 9474 |
rs760950594 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198003 | ATCAGCAATAAAAAC[A/G]ATTAACCTCTTCATT | 9474 |
rs760954351 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232192 | TTGACGGCCAGGAGG[A/C]TAACTGTCTCCTGGA | 9474 |
rs760956378 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220480 | TATGAAATGTCAAAC[A/G]AAATTACCCAGGCTC | 9474 |
rs760957099 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311942 | TTCAAGTGATTCTCC[C/T]GCCTCAGTCTCCCAG | 9474 |
rs760973102 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216916 | ATAAATAAATAAAAG[A/G]GTGACCTCTGTAGTA | 9474 |
rs760980507 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272339 | ACTCTCTGTTCCTCC[C/T]GCCAGGGATTAAGTT | 9474 |
rs760982542 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258489 | GACTTTTATCAATAA[C/T]TTATACACTTGTAAA | 9474 |
rs760990097 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322329 | TAACCTACTACCTGA[A/C]GTAATTTTCACTGAC | 9474 |
rs761027096 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190067 | ATATACCATGATATA[C/T]AAAATAATAAAATAT | 9474 |
rs761034043 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260048 | TCACTCATAGGGGGG[A/G]ACTGAAAAATCAGAC | 9474 |
rs761072171 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185395 | AATGTAATGCACAAA[A/T]ATGTTTGACTGGTAA | 9474 |
rs761090122 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319004 | AGTAGAAGTTAGAAA[C/T]GTAAAATGTGGAGCC | 9474 |
rs761101471 | in-del | -/CTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306808 | CTCTGTTTACACTTC[-/CTTT]CTTTAAGTCGCCTTC | 9474 |
rs761121388 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184581 | TTTACTCTTCCTCTA[A/G]GGCATTGTAGGCTTG | 9474 |
rs761128910 | in-del | -/GA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243530 | AGACCCTCTCTGGGG[-/GA]AAAAAAAAAAAAAAA | 9474 |
rs761233239 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256083 | GTCATAAGGTAAAAA[C/T]AAAAATATTTTAATT | 9474 |
rs761236991 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323894 | CCACCTAAGTATCCA[A/C]TACTTCTTTCCCTCT | 9474 |
rs761248307 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207027 | ATACCACAATACCTG[A/C]TCTTGCCACATATTT | 9474 |
rs761254938 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302117 | GGCTAAAAAGAACCA[-/C]AAAAAAGGTCATAGT | 9474 |
rs761286247 | snp | A/G | 1.65105e-05 | 0.00287315 | synonymous-codon, missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316101 | AATCAATGTACTTAC[A/G]TAGTATGGTTCTGCT | 9474 |
rs761308258 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227381 | TGGGAGGATCACTTG[A/C]GGCAAGGAGTTGAAG | 9474 |
rs761329826 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240025 | TGAGACGGGGTCTTG[C/T]TCTGTTGACCAGGCT | 9474 |
rs761360291 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267292 | AACTTACAAGTGACA[G/T]GAAGGACCTCTTCAA | 9474 |
rs761381315 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303569 | TCAGTTTATAAAGCC[C/T]GTATAACCCTAATGC | 9474 |
rs761408773 | in-del | -/TCTC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246371 | CTCTCTCTGTCTCTG[-/TCTC]TCTCTCTCTCTCTCT | 9474 |
rs761409884 | in-del | -/CAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287580 | CAAAACGCACCAAAT[-/CAG]CACCATGTTACCAAG | 9474 |
rs761429540 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193947 | TAGTTGTGCAAGTGT[A/G]TGTTTCTCATTTTGG | 9474 |
rs761434306 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213047 | CATAGGTACAACAAC[A/G]ACTACTACTACTAAC | 9474 |
rs761531809 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223642 | ATTCACTATAGGAGG[-/A]AACAGTCTCTGAGAA | 9474 |
rs761584168 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207014 | TGCAAACAGGAATAT[A/G]CCACAATACCTGATC | 9474 |
rs761593347 | snp | A/C | 3.30431e-05 | 0.00406454 | intron-variant | ATG5 | GRCh38.p7 | 6:106202101 | TTGTCTATTTGAAAA[A/C]GGAAAAAATGATTCA | 9474 |
rs761601442 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283456 | GCTGGAGTGCAGTGG[C/T]TACTCACAGGTGCAC | 9474 |
rs761610982 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251992 | GTTATAGGCATGCAT[C/T]ATCACGCCCGGCTAA | 9474 |
rs761612124 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231127 | CCCCCTCCAAGCGGT[A/G]GGAGGAGAATTCGGC | 9474 |
rs761629069 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189240 | TAAGCCAAATGTATA[C/T]GCTATCCTTAATTCA | 9474 |
rs761646243 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314787 | AAATACCTCTAACAA[A/G]TGAAATTCTTCTAAA | 9474 |
rs761658899 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202907 | AGCTCAGGCAATCTG[C/T]CGGCTTCGGCCTCCC | 9474 |
rs761660504 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292042 | GATGGGAAAGAAACT[C/G]AGACACCTAAATGAC | 9474 |
rs761680687 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307537 | TGATTTCAATACCCT[-/TT]TTTTTTTTTTTTTTT | 9474 |
rs761697434 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193838 | AATGAAGCCCCATAG[G/T]ACCTGTTTCAATGAA | 9474 |
rs761708449 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228717 | GGACCACTTTTGCTT[-/G]GCTACTCTGGCCTAT | 9474 |
rs761712118 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201071 | ATATTTAATGCAATG[C/T]AAATCTATATAAATA | 9474 |
rs761713346 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243438 | AAGGCTGAAGTGGGT[A/G]GATCGCTTGAGCCGG | 9474 |
rs761718536 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305279 | ATAACTAACTTTACT[A/G]TATGTACTATTTCTT | 9474 |
rs761736531 | snp | A/C/G | 3.29713e-05 | 0.00406015 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106201992 | GGATCAATAGCAGAA[A/C/G]GACAAACTTCTTTGA | 9474 |
rs761773863 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291690 | TTAACAGAAAAGACT[C/T]GTTAGGCAATATAGC | 9474 |
rs761796441 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230194 | AATTGGTCTCCTCAA[A/C]TGTCAGAGCTGTTTG | 9474 |
rs761836667 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268387 | GAAACAACAGATGCT[A/G]GCAAGGTTGTGGAGA | 9474 |
rs761858309 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256979 | GCTTAAAACAAACAC[A/G]TACAGCCGCATAAAA | 9474 |
rs761867895 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211563 | AAAATAAAAAAAATT[A/C]GCCGGGAGTGGTGGC | 9474 |
rs761875207 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222833 | AGTAACAGCATTTAA[C/T]CCAGAGGACAATAAG | 9474 |
rs761893823 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268944 | TGCAAGGCTTAAAAC[-/AT]AGATGACGGGTTGAT | 9474 |
rs761897076 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287790 | CAAAGAGAGAAAAAA[A/T]TTTTTTAATTTTAAA | 9474 |
rs761915300 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254149 | CTAGAATCCCCACTT[G/T]CCTAATCTTTACATA | 9474 |
rs761918751 | snp | C/T | 1.66056e-05 | 0.00288141 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279702 | TTGTGATCTTTTTTC[C/T]GCATTTCATTGATTA | 9474 |
rs761972546 | in-del | -/TTAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189001 | ACCGAAGTTTCTCTC[-/TTAT]TTGTTACTCTGTCCC | 9474 |
rs761987255 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310023 | TCACTCAAAATTGCT[-/AA]AGAACTCACAAATGA | 9474 |
rs761991601 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253087 | ATATAGACCCATATG[A/C]ATTAATTTCTTCATA | 9474 |
rs762007033 | snp | A/G/T | 3.49401e-05 | 0.0041796 | intron-variant | ATG5 | GRCh38.p7 | 6:106248286 | TAAAAATGAACAACA[A/G/T]TATAATGGAATACCT | 9474 |
rs762016972 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264538 | CCAAGACACATAATC[A/T]TCAGATTCTCTAAGG | 9474 |
rs762020325 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295863 | GCCACTATGTCCAGC[C/T]CAAATAACTCTTTAA | 9474 |
rs762092045 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313914 | AAAATTTGGATTGTG[C/T]CATATGGTTTTAAAT | 9474 |
rs762106670 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300023 | AAACACAAACAACTA[C/T]AGAGTAGCAATGTGT | 9474 |
rs762123774 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286090 | TACTAGACCTTGCAG[A/G]GTATCAGCTATGCAT | 9474 |
rs762161623 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300975 | ATTTCGTGCTTGAAG[G/T]TCTAAGATCTAAACC | 9474 |
rs762206517 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197956 | AGCCAGTGCTGCCAC[A/G]GACAGGTAAGAGGTT | 9474 |
rs762224258 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187058 | AAAATGACAAGTACA[G/T]GAAGTCGGTCCATAC | 9474 |
rs762251279 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309016 | CCTGGTCAGTGTTTT[C/T]TCCCCAGAAAAGGTA | 9474 |
rs762253344 | snp | C/T | 1.67161e-05 | 0.00289098 | intron-variant | ATG5 | GRCh38.p7 | 6:106316061 | TCTTACAAAAATGGA[C/T]AAGGTTAAATATCCC | 9474 |
rs762272747 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316374 | AAAGATTATCCACTT[-/C]AAAAAAAAAAAACGA | 9474 |
rs762278628 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322778 | ATACATTTACACTCC[-/CA]CAGTTTTATCTTCTG | 9474 |
rs762292296 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200352 | CAATTCAGAATACAT[G/T]CGTAAGAAACAAGCA | 9474 |
rs762298283 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201576 | AATTCAAATAAAATA[C/T]TCATCCATTTTTCAG | 9474 |
rs762371414 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262670 | ACCCAGGTCATCTTG[C/T]TGGGACCGGTTAGGC | 9474 |
rs762385681 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291762 | CCTCTCTAAACTTAA[A/G]TTGTTGTATATGCAA | 9474 |
rs762400307 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215381 | AGGAATGGTCTATGG[A/G]TTCTGTGGTGAACGC | 9474 |
rs762425550 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321804 | GTCTCCTGCCCCTCC[A/C]CACATTGAACTGGGA | 9474 |
rs762450457 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235707 | GGGAAGGACAATGAT[C/T]GGGATATAAACCCAG | 9474 |
rs762478243 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229013 | TCTCTACTCAACAGT[C/T]GCCCATGCGTGCGCT | 9474 |
rs762490992 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226224 | ACTCACCAAGCAGTA[-/AC]TTTAGGGGCCTGTGT | 9474 |
rs762501154 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257254 | CCTTCCTATTTTACA[C/G]CTAACTTTTTCTAAT | 9474 |
rs762501872 | snp | C/T | 1.65127e-05 | 0.00287334 | utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316229 | CAGGAGTTAAAGCAG[C/T]ACATACAGGCTAAAT | 9474 |
rs762503595 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214332 | AGAGGGGAGTGGGTG[C/G]GAGTCTGTAGCACTT | 9474 |
rs762546457 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204123 | AGGAGAAATACCTAA[C/T]GTAGATGAGGGGCTG | 9474 |
rs762554124 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258121 | ATGCTTGATGGCTCA[A/C]GTCCTTCCCACCCAC | 9474 |
rs762615207 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324309 | GCGCATTATAAATAA[C/T]GCAGAGTTGAACTAA | 9474 |
rs762640445 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316404 | ATGATCACCAATCTT[C/T]AGTATAAATTCAAAG | 9474 |
rs762646934 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276578 | ACACTTAATCATTAT[-/C]CTCCATACCCAATCT | 9474 |
rs762650486 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284876 | TTATCAAGTTATTTC[C/T]ATATTCCGTATATTA | 9474 |
rs762658215 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238148 | TTTACATATGAGATA[A/C]AAATCATATTTTTAA | 9474 |
rs762662557 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226033 | GCCCTAAACTCTCAC[C/G]TATGGGAAACCCTGA | 9474 |
rs762676066 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291349 | CAATGACAACTAGTA[C/T]AGTGAGGTACAATGC | 9474 |
rs762676869 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279590 | TCTAAAATGTATCAA[A/C]TACTCACAGGGTTAT | 9474 |
rs762702894 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317674 | AGCGAATGATATACA[C/T]GCATGTAAACTTCAT | 9474 |
rs762716177 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195422 | ATACTACAGGTGAAC[C/T]GAACCAGGCAGTAAA | 9474 |
rs762764900 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274105 | GCCAACCCTCCCCGC[A/C]TTTTTGGGATTGTAT | 9474 |
rs762774021 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292746 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACCAA | 9474 |
rs762781520 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232396 | CAACTCCCTTGTTAG[C/G]GAGAGACATTCTAGC | 9474 |
rs762788513 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191640 | CAAAGTACTCAGCAG[C/T]GACCCTAGCACAGGA | 9474 |
rs762829114 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221566 | TGGTGTGCGCCTGTA[G/T]TCCCAGCTACTAGAG | 9474 |
rs762847009 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190198 | TAATTGGATAATTTA[G/T]AAAGGACAAACATTT | 9474 |
rs762848558 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248699 | ACAGCACTTTAGGAG[A/G]AGGCTGAGGCGGGCA | 9474 |
rs762860357 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231328 | AATGACAGAAGTGTC[A/G]CCGTAACTGCAGCCT | 9474 |
rs762884838 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260568 | GTGTTCATTTTACCC[-/CT]CTTTTTCATAAGTTG | 9474 |
rs762937044 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251566 | ATTAACTTTAATCTT[C/T]TTATAGAAACGCTAT | 9474 |
rs762947793 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324227 | TGAACATGTATAGAC[C/T]CTTTTTTGTCATTAT | 9474 |
rs762972695 | snp | C/G/T | 3.30908e-05 | 0.00406749 | intron-variant | ATG5 | GRCh38.p7 | 6:106202118 | GAAAAAATGATTCAA[C/G/T]CAATTAAGTCTTTGT | 9474 |
rs762972989 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235484 | TGTTGAGTGGGGGGA[-/C]TGAGAGACAGGATTA | 9474 |
rs762974355 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293971 | TCAGATTTCAGCTTT[G/T]TTTTTTTTCTTCAAA | 9474 |
rs762976942 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310269 | AGAATACTCATTTTT[-/A]AGGCAGAATCCACAC | 9474 |
rs762990632 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280984 | AATTTAAAAGGAGCT[-/A]AAAAATGGCAAAAAA | 9474 |
rs762992833 | snp | C/T | 6.59326e-05 | 0.00574125 | synonymous-codon, missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202021 | GAGGAGATCTCCTAG[C/T]GTGTGCAACTGTCCA | 9474 |
rs763024965 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185932 | TATTAAATGACAAAA[C/G]ATATTTAGAGGCTTT | 9474 |
rs763029527 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233286 | GATTCCTTGACATAA[C/T]AGGTTTCTGCCAAAT | 9474 |
rs763077226 | snp | G/T | 1.65828e-05 | 0.00287943 | intron-variant | ATG5 | GRCh38.p7 | 6:106292986 | GAAGTCTATTTATTA[G/T]GTATCACAAATGGGA | 9474 |
rs763087485 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319780 | GATCATATCTCATTC[A/G]TCTTTTCACCTCTGA | 9474 |
rs763100523 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311396 | CCTTGACACGAAGTG[-/TT]TATCTTAAGGCAAAG | 9474 |
rs763114659 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229866 | TGAGCACACCTCACC[A/G]GTTCAGAATTATTCT | 9474 |
rs763148482 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218368 | ATTCCCCAGAAATCA[C/T]AGTTAAATGAAATCT | 9474 |
rs763191691 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251108 | ATGGGCGCTTGCCCT[C/T]ATCAACATCTCAATT | 9474 |
rs763241887 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299203 | AACCCTTATATTAAA[C/T]GGCATAGTATTTGCA | 9474 |
rs763267582 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281498 | TTCCTGTTACTACAC[-/AT]ATCAGTAATTAATTC | 9474 |
rs763396393 | in-del | -/TC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265825 | GACAACGTACCAGAA[-/TC]TCTGAGACACAGCTA | 9474 |
rs763408432 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222110 | TTAAACCATGAGTTT[G/T]GCCAGGATGGTCTCA | 9474 |
rs763424446 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207686 | CTGAAAATCAGACAA[C/T]GTATGGACTTTAAGA | 9474 |
rs763432042 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310207 | TGCTGAATGAGTCAG[A/C]GATGCCAATGGTTAA | 9474 |
rs763432054 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283265 | TAATTTTCTTTTAAT[G/T]TCTTTATCAGGTTTC | 9474 |
rs763487492 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219482 | TTTTTGTACCAAACA[G/T]GTACAGGCTTTTTTT | 9474 |
rs763493508 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188949 | TAACACAATTTTAAA[C/G]AGAGGGATTCTTAGA | 9474 |
rs763510475 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261435 | AATAAGTCATTATGA[C/T]AACAGGACATACTAG | 9474 |
rs763565140 | snp | C/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327504 | CCAGGAGTTCAAGAC[C/G]AGCCTGCACAACATG | 9474 |
rs763566139 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197746 | CCTGAGGGTCTCATG[A/G]GATGCCCAATCTCCA | 9474 |
rs763583695 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238990 | TTTCTAATTAGAAAC[A/G]CTAGAAGGAAATCAC | 9474 |
rs763602075 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205797 | CCCCAGTGCTATTAC[A/G]TAGTGTAGCTAAACG | 9474 |
rs763615580 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315158 | AGTAATCTGACTTTC[C/T]GTAGCTGGAGCAGGC | 9474 |
rs763631009 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248085 | AAGAGTTCTACACTA[C/G]AGTGCTTCAATTAAG | 9474 |
rs763638662 | snp | A/G | 3.30404e-05 | 0.00406437 | intron-variant | ATG5 | GRCh38.p7 | 6:106293021 | GGAGAAATGCAATTT[A/G]CTATACCTTAAAATG | 9474 |
rs763669270 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288747 | TTAGTAAGAGACACA[C/G]GTAACTTGAAAGCAC | 9474 |
rs763696995 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324699 | TCCCCCAATTTTAAG[G/T]AGCATATCTTTGAAG | 9474 |
rs763708645 | snp | C/T | 4.94588e-05 | 0.00497262 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106201984 | TACCTTCAGGATCAA[C/T]AGCAGAAGGACAAAC | 9474 |
rs763759071 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263219 | CTGACAGTGCTAAGG[A/T]GTCTGGGAGGTCTGG | 9474 |
rs763765270 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264890 | GCCACTGCAAAAAAC[-/A]CACCAAAATATAAAG | 9474 |
rs763780296 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232620 | AGGCTCAACAAGGAC[C/T]CCAAAAGATTAAGGA | 9474 |
rs763790196 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187586 | ACCTTCTCTTCAAAA[C/T]ACAATGTCTAAACCT | 9474 |
rs763791644 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295755 | TTTTTATAGAGATAG[C/T]GTCCAACTATGTTGC | 9474 |
rs763793860 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280122 | GCAAAGATGTGGAAT[A/G]GAGCCCTCACACACT | 9474 |
rs763794297 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289953 | TGTAGTTTAAAAGAA[G/T]TATTTTAATAGCCTT | 9474 |
rs763800255 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310409 | TATAGTACATATAGA[C/T]ACAATTTACCTAGGA | 9474 |
rs763802441 | in-del | -/A | 1.83363e-05 | 0.00302784 | intron-variant | ATG5 | GRCh38.p7 | 6:106279870 | GGATACACACATTAC[-/A]AAATTAACCTCTTAA | 9474 |
rs763810013 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243097 | TTTTCAAAAATGTAC[C/T]TTTTCTCTCCCCAAA | 9474 |
rs763826710 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240444 | ACAGTGCAATTTACA[A/G]AAAACCAAGTCCAAA | 9474 |
rs763827614 | snp | C/T | 1.65891e-05 | 0.00287998 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186529 | TTCTGTTCAGGCAAA[C/T]AGTTGATCCTTCAAT | 9474 |
rs763881439 | snp | C/T | 1.67058e-05 | 0.00289009 | intron-variant | ATG5 | GRCh38.p7 | 6:106186680 | TTTTTTCCCCATCTA[C/T]TCCAAGAAAGAAACC | 9474 |
rs763928175 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249097 | CTTTTTAAAAACTTT[C/T]CAATTTCAAATTTTT | 9474 |
rs763942930 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200982 | GCTCAAGTCGCTTAT[A/G]TAGAATGGCATAATA | 9474 |
rs763958477 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255923 | ATAACCTCCTGTTCT[A/G]TTACTTTTTAAAACT | 9474 |
rs763962789 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303297 | AAACAACTCTATGTT[C/G]ATAAATTAACAACTT | 9474 |
rs764013292 | snp | A/T | 1.71563e-05 | 0.0029288 | intron-variant | ATG5 | GRCh38.p7 | 6:106248270 | ATAAATTATTTGTTA[A/T]TAAAAATGAACAACA | 9474 |
rs764059395 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254377 | AGTCCCATGAGGGCA[A/G]AGACTTTATCTTCAG | 9474 |
rs764072139 | in-del | -/GGGC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286311 | GTTCCAAAGCACATG[-/GGGC]TCACCTTGTTTGTTC | 9474 |
rs764106345 | in-del | -/AATA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201658 | GACTTCTTTAAAGTT[-/AATA]AACAAAATGCAAGAT | 9474 |
rs764112604 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318143 | TAGAAAATATAATCC[A/C]AGACAATTGCTCTTC | 9474 |
rs764132804 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286846 | TACAACCATAGGATA[C/T]GAATTCTGCCAGCAA | 9474 |
rs764201221 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238703 | ACTTCGACCAAGAGC[C/T]CTGCCAGGTATTGAT | 9474 |
rs764212573 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269984 | AGTATAATCTGTATT[C/G]CACTGCGAAATAACT | 9474 |
rs764239623 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305091 | AGCAAAACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 9474 |
rs764256800 | snp | C/T | 3.31225e-05 | 0.00406941 | intron-variant | ATG5 | GRCh38.p7 | 6:106202131 | AAGCAATTAAGTCTT[C/T]GTTGCTGCCAATTAC | 9474 |
rs764281192 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196100 | AAAAAATTCAACAAG[A/C]GTGGTCAGGATTATA | 9474 |
rs764292305 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220592 | TATATTACCTACTTA[A/G]AATTATTAGCAAATA | 9474 |
rs764322101 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299168 | GGACCTAGCTGGATA[C/T]CAAAATTCGCAGATG | 9474 |
rs764329081 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246036 | GAAATGGCAAATTAG[C/T]AAAAACTGGACTCCT | 9474 |
rs764343948 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312826 | AAAAAAATACCATTA[A/G]TGACTTTGGCAAGAA | 9474 |
rs764393438 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185995 | TTACAAGATTGCATA[A/C]CAATAGACAGACTGT | 9474 |
rs764395454 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212467 | CCAATATGGTGAACC[C/T]GTCTCTAACAAAAAT | 9474 |
rs764413466 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189144 | GAATGCTTTCTGATA[C/G]CTAGCCCTACCATGG | 9474 |
rs764423278 | in-del | -/AAATGACAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245132 | ACTAAACTGTTATGT[-/AAATGACAG]AAATGACACATTTTG | 9474 |
rs764500943 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283406 | ATTTTATTTTATTTT[G/T]ATTTTTAGAGACAGG | 9474 |
rs764507923 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307837 | GTTCTTATCAGTTCA[A/G]TACCCTTCTTAAAAA | 9474 |
rs764524611 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324472 | ACTGTACCTTAATTT[C/T]TGTATCAATGTCTTC | 9474 |
rs764549228 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185447 | AAGTGCAGCAAACTT[C/T]CCTTATATTGAATAA | 9474 |
rs764596571 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213125 | AGGATCTCTAAGTAA[C/T]GATCAGAAGGCAGGA | 9474 |
rs764598960 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272413 | CTCTGCCTGACTTCC[A/G]GTTTGACCTCCTTAC | 9474 |
rs764600970 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258525 | TAGCAATTTAAAAAA[A/C]CCTAGGATTTTATAT | 9474 |
rs764673538 | snp | G/T | 1.74045e-05 | 0.0029499 | intron-variant | ATG5 | GRCh38.p7 | 6:106293149 | AAATAAATATTTAAA[G/T]TTATAACTACAAGGC | 9474 |
rs764689974 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225724 | TTTGATCTGCCAGTT[A/C]CCTAGAAAAACCTCC | 9474 |
rs764715287 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303639 | CTTATGAACATAAGA[C/G]ACAAAAATCCTCAAC | 9474 |
rs764732487 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228334 | CAGGGTGTCCGTTGT[A/G]CTCCTGATCCAGTGA | 9474 |
rs764737182 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315234 | GGCAGACTTCATTAA[A/C]GTGAAACAGAAGAAG | 9474 |
rs764748125 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225961 | CATATTTCTGATAAT[C/T]CAGAAAGCCATACAC | 9474 |
rs764764941 | in-del | -/AAC | 6.92329e-05 | 0.00588317 | intron-variant | ATG5 | GRCh38.p7 | 6:106248279 | TTGTTATTAAAAATG[-/AAC]AACATTATAATGGAA | 9474 |
rs764768207 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290517 | GTAGAGATGGGGTCT[A/G]CGTTGCCCAGGCTGG | 9474 |
rs764810506 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254625 | ATTTATTTAATAGTT[A/G]TGTGAGTTTTAGCAA | 9474 |
rs764848356 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234992 | GTTGTTATTATGTTA[G/T]TTTAGCGGAAGAATG | 9474 |
rs764872534 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202170 | ATATCATAAACTTTA[-/T]GTTGGCATTAGGTGC | 9474 |
rs764898118 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256203 | TCCTTTATGCTTCTG[C/G]AGAGAAAGTGTAAAG | 9474 |
rs764948788 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219779 | AACTAGTATAATTTT[A/G]TGTTGTTCACATAAT | 9474 |
rs764984175 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269412 | CGTGCCCCGCACTCC[G/T]CAGCCCTTGGGTGGT | 9474 |
rs765001417 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262570 | CGAGTTGATAAGATG[G/T]CTGAATAGGAAAAGT | 9474 |
rs765003298 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243465 | CCGGGAAGGCAGAGG[C/T]TGTAGTGAGCTGAGA | 9474 |
rs765039569 | in-del | -/ACATATGTGTATATATACATA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208254 | GTGTATATATACATC[-/ACATATGTGTATATATACATA]TGTGTAAACACATAT | 9474 |
rs765091363 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276833 | AATATCATTTAATCT[C/T]CAAATCACCAGCAAG | 9474 |
rs765094034 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322989 | CAGTGGCGCAATCTC[C/G]GCTCTCTGCAAGCTC | 9474 |
rs765109542 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244611 | GCATTAGGTTTTTAT[C/T]GCACTGTATGTCTCT | 9474 |
rs765191792 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243463 | AGCCGGGAAGGCAGA[A/G]GCTGTAGTGAGCTGA | 9474 |
rs765195827 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188296 | TTTGAAAACATTTCC[A/G]GTATAATTCTCTTCA | 9474 |
rs765214986 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201247 | TATGTATTATACACA[C/T]ATGTATATCTCAAGT | 9474 |
rs765218463 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214147 | AAGATATATTCATGC[A/G]TATCAAATTTTACAT | 9474 |
rs765220096 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185715 | AAAGATGAACAGTTA[C/G]AATATTTATACGTGT | 9474 |
rs765222809 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308723 | CATAAATGCCCAGAA[C/T]GATCAACACAAATCT | 9474 |
rs765322962 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321892 | TTAGCACATAGTAGG[C/T]TTTGAAATTTTTGTT | 9474 |
rs765342023 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198455 | GACAGGAATTCACCA[A/C]AATTAAATGCTTTTA | 9474 |
rs765346738 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239180 | AAAAAAAAAGTTTGT[A/G]AAAACACAATAGGAT | 9474 |
rs765372877 | in-del | -/AAGAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245587 | TTTTGAGGCTTCAAC[-/AAGAT]AAGATGGGCCTCACT | 9474 |
rs765393466 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197128 | GGGTTTCATTGCAGT[A/G]TTCTCATTCTATAGT | 9474 |
rs765396392 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106184700 | CTTTCAAATCTAGAT[C/G]AGAAGTTCACTCAAG | 9474 |
rs765401015 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287844 | TTTTAACTGTAATGT[C/T]GCTTTGCAAGCAGCA | 9474 |
rs765410072 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257594 | CAGGGATCTAGGTTC[A/C]AATTCTGGTTCCACC | 9474 |
rs765419687 | snp | C/T | 1.65548e-05 | 0.002877 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279718 | GCATTTCATTGATTA[C/T]TTGACTTTTATGTTT | 9474 |
rs765443353 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187905 | GAAAAATAAAAACTT[-/T]AACATACTAACAATT | 9474 |
rs765502523 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271283 | TGTTTACATCCCCCT[A/G]TAATTCATGTTGAAA | 9474 |
rs765509735 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286957 | ATAACCTAGGCAGAA[A/G]ATCCAGGTATAAGCT | 9474 |
rs765548765 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208019 | ATTGCTTGAACCCAG[A/G]GGGCGGAGGTTGCAG | 9474 |
rs765565260 | snp | A/C | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326232 | AAGACTATATGAGCA[A/C]TGAACCCTCCCACCC | 9474 |
rs765608348 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294621 | TGAAGTCAGGAGTTC[A/G]AGACCAGTTCCAGTA | 9474 |
rs765611277 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325753 | CAGCGAATACAACCG[A/G]CAACGCTGCGGAGCC | 9474 |
rs765627861 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194069 | TGTCATCATTTCCAG[C/T]AGTGGAGAATGAAAA | 9474 |
rs765659398 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249745 | TGTATTTGGATTCCA[A/G]TTAGTCCACATCCTT | 9474 |
rs765670760 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218615 | ACTTTGATGTGTAGA[C/T]CCTTTGAAAGCCACT | 9474 |
rs765677951 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309054 | ATAAAACAGGAGTGT[C/T]TTGGAAAATCAATTA | 9474 |
rs765682742 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205950 | TTAATATTTATTATA[C/T]AGTACCTTTAAAAAC | 9474 |
rs765684767 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282171 | AATGGACCAGCTACT[C/T]CAATTCATGTTATGA | 9474 |
rs765699605 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254412 | AGAAAGTTCTACGTA[C/T]TTCAGCCCTAGAAAG | 9474 |
rs765747213 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248297 | AACATTATAATGGAA[C/T]ACCTCACATGAAGAG | 9474 |
rs765789943 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291838 | ACCAACACTATGTGC[A/T]CTATCTGTACTGTTC | 9474 |
rs765857129 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201940 | AGTAACAGAAAATGA[A/C]AGAAATGTTTTAATG | 9474 |
rs765886568 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218260 | TAACTATCAACCAAA[C/T]TATAGAAAAGAGTGC | 9474 |
rs765895694 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306638 | AAGCCCCGCTAGTCA[A/C]ACAAAATTCTGAGAT | 9474 |
rs765899258 | snp | C/G | 1.65241e-05 | 0.00287433 | utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316235 | TTAAAGCAGTACATA[C/G]AGGCTAAATTCTTAT | 9474 |
rs765911598 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276923 | TTGTGAACTCAGTAA[G/T]AAAAATGTGGTACGG | 9474 |
rs765987487 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214387 | TAGAGAAATAGGAGA[C/G]TTGAAAATAAGCACT | 9474 |
rs766003597 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226051 | TGGGAAACCCTGAGG[C/T]TCTGTACAAGAAGAA | 9474 |
rs766036540 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221056 | ATTAGGAAACTAAAG[C/T]CCATGTCAACCAATG | 9474 |
rs766056929 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245136 | AACTGTTATGTAAAT[A/G]ACAGAAATGACACAT | 9474 |
rs766062613 | snp | A/G | 1.65466e-05 | 0.00287628 | intron-variant | ATG5 | GRCh38.p7 | 6:106316087 | ATCCCATTTGCCACA[A/G]TCAATGTACTTACAT | 9474 |
rs766079935 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312988 | GGTCAACAGAAGGTT[A/G]TTGTTTCAGGATAGG | 9474 |
rs766087726 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256446 | CTGTACTTTTGAAAG[C/G]TCCCCAGATGATTCT | 9474 |
rs766120406 | in-del | -/T | 1.67175e-05 | 0.0028911 | intron-variant | ATG5 | GRCh38.p7 | 6:106248126 | TTTCATAAATGGATG[-/T]TTTTTTAAAATGTTA | 9474 |
rs766128604 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222451 | ATTCCAGAATTTTAG[C/T]TGTTTCAATCTCTTC | 9474 |
rs766136130 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317998 | TTCACCTTTTGATGA[G/T]GAAGAGAAAAATAAT | 9474 |
rs766147321 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252436 | GCTGAATTAAGCTTT[C/T]ATATTGGTCTTGCAA | 9474 |
rs766153685 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266482 | AAAAAGAGGGACTCC[G/T]CCCTAACTCATTTTA | 9474 |
rs766168826 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324296 | TTTAAGTTGTATTGC[A/G]CATTATAAATAATGC | 9474 |
rs766184169 | in-del | -/GTG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189481 | TAGCTTTAGCTGGGC[-/GTG]GTGGTGGTGCATGCC | 9474 |
rs766199845 | in-del | -/ACACACAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297718 | TGCAAAATGACTTAA[-/ACACACAC]ACACACACACACACA | 9474 |
rs766214165 | in-del | -/CACCCAGTGGATCCCA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269357 | GAGCCCAGCTGGCTT[-/CACCCAGTGGATCCCA]CACCGGGGCTGCTGG | 9474 |
rs766218545 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264542 | GACACATAATCATCA[C/G]ATTCTCTAAGGTTGA | 9474 |
rs766261749 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232439 | CATTATACACCTGAA[A/C]ATAGGAGAACACCCG | 9474 |
rs766279462 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269392 | GCTGCCTGCCAGTCC[C/G]GCGCCGTGCCCCGCA | 9474 |
rs766306451 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263401 | CCTGGGGGAAGGGGC[A/G]GCTGTGGGTGCAGCT | 9474 |
rs766319918 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300059 | AGCTTTCTAAGCCCA[C/T]TCTTATATATGAAAA | 9474 |
rs766383083 | snp | A/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326483 | TGGAGAGTCTGAGGC[A/T]GGAGAATGGCGTGAA | 9474 |
rs766423646 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261484 | CTGGAATAGATGAGA[A/G]ACTTCATAAATGGGT | 9474 |
rs766424168 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218422 | CACAATATTTAACGT[A/G]AACATTTTAAAAACA | 9474 |
rs766459185 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259663 | ATATTAATCCTTTTT[-/C]ATCTTTCAAAAAATA | 9474 |
rs766471609 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310250 | CAACAACTGTAATTT[C/T]AAAAGAATACTCATT | 9474 |
rs766480665 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187372 | AAATTCAATTGTATT[A/C]CAAATTAAACTTAAG | 9474 |
rs766535189 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278030 | GCTCACTGTAACCTT[C/G]AACTCCTTGGGCTCA | 9474 |
rs766535608 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185972 | TCTCTCACTGTTCAT[A/T]ATCAAAGTTACAAGA | 9474 |
rs766562523 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241651 | TTAAATTGGTGGATT[C/G]TGAGTACAGCAGATT | 9474 |
rs766597836 | snp | C/T | 4.95864e-05 | 0.00497903 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279761 | TTCTTTCATACATGA[C/T]ATAAAATGAGCTTCA | 9474 |
rs766624035 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242140 | ATACACACATACTCA[-/CA]CACACACACACACAC | 9474 |
rs766626551 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260384 | TTTGGGATACTTTTA[C/T]ATCCTTCTAACGGGA | 9474 |
rs766653370 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229217 | GAAGCTCTATGCTGC[A/G]CCCTTAGGCATCTAG | 9474 |
rs766654816 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323940 | AGTCAAACTAGCTAG[C/T]ATGCGCCTGCTTCAG | 9474 |
rs766658163 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289545 | TGTAAGATTCTTTTT[C/T]CTATTTGCTAATAAA | 9474 |
rs766685902 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319872 | GTTGGAAAGACAGTG[C/T]ATGAATATAAAACTA | 9474 |
rs766709059 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274113 | TCCCCGCCTTTTTGG[A/G]ATTGTATACTCCGAA | 9474 |
rs766767756 | snp | A/G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300019 | GGACAAACACAAACA[A/G/T]CTATAGAGTAGCAAT | 9474 |
rs766782982 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238926 | ATAAAAAAAAGTGGA[-/G]GGGGGGGAACCCAAT | 9474 |
rs766784336 | snp | A/G | 1.76774e-05 | 0.00297294 | intron-variant | ATG5 | GRCh38.p7 | 6:106248294 | AACAACATTATAATG[A/G]AATACCTCACATGAA | 9474 |
rs766789806 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219506 | TTTTTTTCTTGTTAT[C/T]ATTCCCTAACTACAG | 9474 |
rs766816146 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315422 | GACAGAGGCATAAAC[C/T]GGGATTATACATGCA | 9474 |
rs766821313 | in-del | -/AAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294175 | CACAACAAGGGCAAA[-/AAG]AAGACTACTTGGTGT | 9474 |
rs766897476 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235060 | AAAGTTGAAGAAATT[C/T]GAGATTGAATACAAC | 9474 |
rs766942117 | snp | C/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326311 | CCGGGCGCGGTGGCT[C/G]ACGCCTGTAATCCCA | 9474 |
rs766945180 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207694 | CAGACAATGTATGGA[C/T]TTTAAGAGTAACAGG | 9474 |
rs766980853 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190440 | TGCTGCATTGGGGAT[G/T]AAGCTTCTAACATGT | 9474 |
rs766993928 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324363 | ATCTGCAAACACTAC[A/G]CCATTTTATATCAGG | 9474 |
rs766998319 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206051 | ACAAAAAAATACTCA[A/G]TTTGGGGAGTTAGTT | 9474 |
rs767019539 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292821 | TAATAAAGAAAAGCA[A/G]TTCATATATTAAAAG | 9474 |
rs767041493 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324923 | CAGCTACTGTCTGGT[-/CA]AAGTCTCCGGGTTCT | 9474 |
rs767043615 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191766 | TGATAAAGTATGTGA[G/T]GACAGAAGATCATTT | 9474 |
rs767047510 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327519 | CAGCCTGCACAACAT[A/G]GCAAGACCACATCTC | 9474 |
rs767048909 | snp | C/T | | | utr-variant-5-prime, intron-variant | ATG5 | GRCh38.p7 | 6:106325405 | CTTCACCCGCCATCG[C/T]GGCCGGGCGGGCGCT | 9474 |
rs767057282 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204384 | GACAAGTATGAAAAT[C/T]GTAATTTTTAAAAAA | 9474 |
rs767089983 | in-del | -/GTATAAGA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281799 | ACTCCCACTAGCAAT[-/GTATAAGA]GTTCTGGTTACTCCG | 9474 |
rs767093510 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246904 | TTAATAAATTAGAAA[C/T]TCAAATGCCGGGCAC | 9474 |
rs767164184 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245618 | CACTCAAGCATGCTC[A/G]GTACTCTGTCTCTCT | 9474 |
rs767199763 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301393 | ATTAGAGAGAACAGA[C/T]AAGATGGGAGAAAAA | 9474 |
rs767202200 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216797 | GCAAGAGGATCACTT[A/G]AGCCAGGAGTTCCAG | 9474 |
rs767213817 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198702 | GAATCACTTGAACCC[A/G]GAGGTGGAGGTTGCA | 9474 |
rs767220880 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307694 | GGCATGTGCCACCAC[A/G]CCCAACTAATTTTGT | 9474 |
rs767248771 | snp | C/T | 3.30071e-05 | 0.00406232 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316107 | TGTACTTACATAGTA[C/T]GGTTCTGCTTCCCTT | 9474 |
rs767274216 | in-del | -/AAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242621 | AAAAATACTATAAAT[-/AAC]AACAACAAAAAAAAC | 9474 |
rs767283279 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289229 | CATTGATTTTCTGCC[G/T]GAAAATTAACACTTA | 9474 |
rs767301949 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314306 | TCATGCCTGTAATCC[A/G]GGCATTTTGGAAGGC | 9474 |
rs767317767 | in-del | -/CTCACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246391 | TCTCTCTCTCTCTCT[-/CTCACA]CACACACACACACAC | 9474 |
rs767373122 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265855 | TAAAGCAGTGCTAAG[A/G]GGGAAATTTATAGCA | 9474 |
rs767417728 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314880 | ATATTTCCAAAGTTA[A/G]GATTACTCACGTGTA | 9474 |
rs767419791 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300182 | TATGCCTAGTTTTCC[A/G]TTATTGGAACGCTAA | 9474 |
rs767432077 | in-del | -/AGG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292136 | ACTTGACTTGAGGTC[-/AGG]AGTTCAAGACCAGTT | 9474 |
rs767456250 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288136 | CCACCATGCCCAGCT[A/G]ATTTTTGTATTTTTA | 9474 |
rs767457446 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207332 | AGAAAAACGAAACTT[A/C]TAAACATTTTAGGAA | 9474 |
rs767491667 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311701 | ATGAAAAGCCACAAA[C/G]GTTTTAAGCAAGCAA | 9474 |
rs767530012 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210698 | CAATTAGTACCTATA[C/T]GACCCTAGTCAAATA | 9474 |
rs767546265 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221758 | CAACTTATGTTTACT[A/G]TATCTACTTATATTC | 9474 |
rs767594953 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266327 | TGACTAGAACAATAA[C/T]AAGTTCTGAAATTGA | 9474 |
rs767677189 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215267 | AAATTCTGTTCTCTT[A/G]ATGCCCAGTTAAGTG | 9474 |
rs767705448 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194921 | TTAATGTACAAAGAA[A/G]AAAATATTTCACTCA | 9474 |
rs767718050 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189174 | GAGAATAACTCTACC[C/T]GTAAAGACTGTTTTG | 9474 |
rs767722352 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310532 | CTTAGGTGTATTTCA[C/T]TGGTTTAAGTTCTTT | 9474 |
rs767742860 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276766 | CCTTCTCTCTTTACA[C/T]GATCCTCATCTTTTT | 9474 |
rs767769052 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251245 | TTGCCCTGACTGCCA[A/G]TGTACTACATACCAA | 9474 |
rs767837645 | in-del | -/ACACACATAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297760 | CACACACACACACAC[-/ACACACATAT]ATATTTTAAAGTTCA | 9474 |
rs767866515 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321821 | ACATTGAACTGGGAG[C/T]TCTTTGACAGCAAAA | 9474 |
rs767928229 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233646 | GTATCTGAAGCAGTT[-/A]AAAATAATACAAGGA | 9474 |
rs767930271 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271099 | CTGCTTAAAAGTCCT[C/T]CAATAGCTTAAAATC | 9474 |
rs767932063 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212851 | CTTATAGATCTTTAG[C/T]AAAAACAAAAAAACC | 9474 |
rs767961118 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285254 | AGCAGTTCTACAATT[C/T]TGTGGTTTTTTTAAG | 9474 |
rs767977834 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184401 | TCCAAGAAACTTTTA[C/T]GACAGTTTGTGACTA | 9474 |
rs768015623 | snp | A/T | 1.66643e-05 | 0.0028865 | intron-variant | ATG5 | GRCh38.p7 | 6:106248132 | TAAATGGATGTTTTT[A/T]AAAATGTTATTTCCT | 9474 |
rs768018551 | snp | A/G | 1.65658e-05 | 0.00287795 | intron-variant | ATG5 | GRCh38.p7 | 6:106292998 | TTATGTATCACAAAT[A/G]GGACGAAGGAGAAAT | 9474 |
rs768114280 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230050 | AGGTCCGACCAGACC[C/T]AGGAGGAACTCCCTT | 9474 |
rs768114569 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252219 | GAGGAAGATAATATA[C/T]ATACTTCTCGCCAGA | 9474 |
rs768180310 | snp | A/G | 1.67565e-05 | 0.00289447 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279797 | ATCCTTAGATGGACA[A/G]TGCAGAAGGTCTTTT | 9474 |
rs768198732 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316840 | CCAATACTTCCATTT[C/T]AATTACTGTACTTCC | 9474 |
rs768199606 | in-del | -/CAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208936 | AAAACATATCTCACA[-/CAT]CATTAGCCATTAAAG | 9474 |
rs768274586 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317208 | ATATTGTTGATAATA[C/T]ACACTTAGAGTAACT | 9474 |
rs768275796 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261121 | AAAGAGTGGGAAAGA[A/C]GAGTTGTTAAAATAT | 9474 |
rs768284137 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231998 | AAATAGAAATAAGCC[A/G]CCCCCTCGTCCATGC | 9474 |
rs768319835 | snp | C/T | 3.30158e-05 | 0.00406286 | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202089 | GTCTTTCAGTCGTTG[C/T]CTATTTGAAAAAGGA | 9474 |
rs768321741 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275077 | TACACAAGGTGCTCA[A/G]TAAATATCTGTTGAC | 9474 |
rs768343714 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282880 | CAGCCTCAACCTCTG[C/G]GGCCCAAGCGATCCT | 9474 |
rs768343764 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298375 | AATTTAAACATATGC[G/T]TCCTTAAAATTATAT | 9474 |
rs768389884 | in-del | -/ACACACACACACAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297754 | CACACACACACACAC[-/ACACACACACACAT]ATATATTTTAAAGTT | 9474 |
rs768405498 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219204 | AGTACTACATTGGAT[A/T]TCCGGGTCTTCAGCT | 9474 |
rs768419311 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229640 | TGAAGGTCTTCTCCG[C/G]GACCCTATAACACTC | 9474 |
rs768424040 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188494 | GTCACAACTCAATAT[A/C]CAAAGTACTGTATCT | 9474 |
rs768425122 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317340 | TGAAAACACTCTAAA[C/T]AATCTTACGAGTTTA | 9474 |
rs768432071 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256923 | TAGCTTTTTCACTTT[A/G]TAAACATTTTCAACT | 9474 |
rs768475467 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279114 | AGAGGGTGATCAATG[C/T]AGGCAAGATCACAGA | 9474 |
rs768513416 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106316002 | AGCATGAATTAGCTG[C/T]ATCTAAAACGTTACA | 9474 |
rs768526948 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213971 | GAGAATAAAAAATAA[C/T]TGGTATTCTAACTTC | 9474 |
rs768573705 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202890 | CTGGTCTCAAACTCC[C/T]GAGCTCAGGCAATCT | 9474 |
rs768576999 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251781 | AGAAGAAAAGAAAAG[A/G]AGGAGAGAAAATCAG | 9474 |
rs768580097 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215139 | ACATGTTTTATCCTT[C/T]TGGTGTACTTACATA | 9474 |
rs768642298 | snp | A/C | 1.65021e-05 | 0.00287241 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293072 | GAGCTGAACTTGATG[A/C]AAGAAGATCAAATAG | 9474 |
rs768663141 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268234 | GGATATGAGCAGGCA[A/C]TTCTCAAAAGAAGAC | 9474 |
rs768674686 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222552 | AGGGCAGTAAGCAAC[C/T]GAAAAGGAAGAGTAA | 9474 |
rs768685177 | in-del | -/ATGA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302173 | TACAGGAGGGAATAT[-/ATGA]ATGAATAATTAATTA | 9474 |
rs768685906 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253080 | CATTCAAATATAGAC[C/T]CATATGAATTAATTT | 9474 |
rs768690103 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106325104 | TAGCACTAAATATTG[C/T]TATTGAGACAGGGAA | 9474 |
rs768728245 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211446 | CCGGGCGTGGTGGCT[A/C]ACGCCTGTAATCCCA | 9474 |
rs768773845 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264503 | GAACACCACTAAGAT[A/C]CTCCTAAAGAAGAGC | 9474 |
rs768824151 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279447 | TATGTTAGGGGCTGA[C/G]CAATCAGTCTAATGC | 9474 |
rs768842958 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280727 | TAATCCTAACAACAC[-/TT]GAGGTAAACATTATT | 9474 |
rs768845169 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265736 | ACATGAAAACCGCTC[C/T]TAAATAACTACTTGG | 9474 |
rs768879024 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280978 | TTTAATAAATTTAAA[A/G]GGAGCTAAAAATGGC | 9474 |
rs768896567 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319595 | CTTTCAACTTAAACA[C/T]GCTTTAGGACCCAGC | 9474 |
rs768920976 | in-del | -/TA | 1.64909e-05 | 0.00287144 | intron-variant | ATG5 | GRCh38.p7 | 6:106201965 | TAATGTTGCTGATTG[-/TA]TATTACCTTCAGGAT | 9474 |
rs768933198 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199582 | AGCTACAAGTAAGTA[C/G]AAGGAGATGGAAATG | 9474 |
rs768944196 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323096 | GGTTTGTTTTTTTTG[G/T]TTGTTTGTTTTTTTG | 9474 |
rs768948286 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195021 | GAGCTCACCTTTGGT[-/C]ATTTCCTGTTACCTC | 9474 |
rs768970159 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273328 | TCTATGTTACCACAG[G/T]TATTTCTGGAAAGTT | 9474 |
rs769022755 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316158 | TAGCGTGAAACAAGT[C/T]GGAATTCGTCCAAAC | 9474 |
rs769059924 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288962 | TGTGGCAGAGGCAAC[A/G]GGATCTCTTAGAAGC | 9474 |
rs769087447 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228974 | CCCGGCATTAGCCGG[C/T]TGAGATCATGTCGCA | 9474 |
rs769087514 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285686 | CTAGGCTGTTGTAGC[C/T]GCAAAGCAGTCATAG | 9474 |
rs769147430 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106198027 | CTTCATTACACTTCA[A/C]ATGAAAATAACTCAT | 9474 |
rs769156145 | in-del | AG/TCCCACTCTAGGCACTCCTTAACCACACCCAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196810 | ACCCAACTAATTTCT[lengthTooLong]AAACTAGAAATTGGC | 9474 |
rs769166515 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196552 | AACATGGTGAAACCC[C/T]GTCTCTACCAAATAT | 9474 |
rs769170120 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287771 | GCACTGTTCTCAACA[C/T]GGACAAAGAGAGAAA | 9474 |
rs769186185 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253989 | CCCCTTGGAAAGTTA[C/T]TGCTGCATTTCTCTG | 9474 |
rs769204914 | in-del | -/G | 5.19615e-05 | 0.00509687 | intron-variant | ATG5 | GRCh38.p7 | 6:106308498 | AAAAGCAACTGAAAT[-/G]GAAAATTTGTAAAAC | 9474 |
rs769210223 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212276 | AGATTTTACAATTTA[C/T]AACTCTAATAAAACA | 9474 |
rs769218956 | in-del | -/ACACACACAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312624 | CTGGCAAAAAAGACT[-/ACACACACAC]ACACACACACACACA | 9474 |
rs769232060 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317589 | TATTAAACTGAGTCC[A/G]GTGCTCTTTCCAGCA | 9474 |
rs769238952 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237646 | CTACATCCCATAATA[C/G]TTTGTTGTACAATTT | 9474 |
rs769250707 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302248 | TCAAATTAGATGAGC[A/C]AAGAAACGGAAGCCC | 9474 |
rs769262921 | snp | A/T | 3.66441e-05 | 0.00428027 | intron-variant | ATG5 | GRCh38.p7 | 6:106308516 | AAATTTGTAAAACCG[A/T]ATTTATTTACTAGTT | 9474 |
rs769378713 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195388 | GTGTCAAAATGCTTC[A/G]TGTTTGACACATCTG | 9474 |
rs769462515 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262903 | GCCCTGGGTTTCAAG[C/T]ACAAAACTGGGCAGC | 9474 |
rs769470089 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251966 | CCACCTCAGCCTCCC[A/G]AGTAGCTGGGGTTAT | 9474 |
rs769485588 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268464 | CCATTGTGGAACAGT[A/G]TGGCAATTCCTCAAG | 9474 |
rs769553121 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300934 | TTATTTATTTTACAG[G/T]TGACAAAATGAGAAG | 9474 |
rs769573619 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306586 | AAAATGTCAGTAGTG[A/T]CCCTATTGAGAAATC | 9474 |
rs769601726 | in-del | -/CTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307535 | TTTGATTTCAATACC[-/CTT]TTTTTTTTTTTTTTT | 9474 |
rs769616432 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226832 | AAAAGCACAAAAACT[G/T]AATTAACTTGAGGGG | 9474 |
rs769631239 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106248201 | TTCTTCTGCAGGATA[C/T]TCCATGAGTTTCCGA | 9474 |
rs769649780 | snp | C/G | 3.30846e-05 | 0.00406709 | intron-variant | ATG5 | GRCh38.p7 | 6:106202115 | AAGGAAAAAATGATT[C/G]AAGCAATTAAGTCTT | 9474 |
rs769655090 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273893 | TGTCGTGACTTGTTA[C/T]AAAATTACCATTAGC | 9474 |
rs769669609 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215253 | TGACCTCAAAAGTGA[A/C]ATTCTGTTCTCTTGA | 9474 |
rs769670482 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237152 | TAATTAAGATTCCAA[A/C]TAATTTTAAAATATA | 9474 |
rs769700428 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241509 | AAATACCCCAAATAA[C/G]TGAAAACAGGGTGTA | 9474 |
rs769727231 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318522 | CGTTCCAGCAAAGTT[G/T]ACCAAAGTTCTACAG | 9474 |
rs769730069 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292708 | GGCTGGTCTTGAAAT[C/T]CTGGGCTCACCTCGG | 9474 |
rs769732812 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324099 | TTTTTTTCTCTAGCA[C/T]TTTCCGCCACTTGAC | 9474 |
rs769748689 | in-del | -/TA | 0.000205353 | 0.0101309 | intron-variant | ATG5 | GRCh38.p7 | 6:106248268 | ATATAAATTATTTGT[-/TA]TTAAAAATGAACAAC | 9474 |
rs769821065 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227934 | CCAACTCAAACCAGG[C/T]AGCAATGAATTGTAA | 9474 |
rs769824002 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212405 | CAGCACTTTGGGAGG[C/T]CAAGGCGGGCGGATC | 9474 |
rs769852783 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199725 | CAGTAGTAAAGATGG[A/G]TTAGGAGTCTAAGAT | 9474 |
rs769873434 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258038 | TAACATGTAGTTGGG[A/G]AAGCCAAATTGACAC | 9474 |
rs769907145 | in-del | -/TC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260296 | ACAAAATCTTGACAT[-/TC]TGAGTGTGGCTTGGA | 9474 |
rs769957025 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224189 | AAGATGTTTAGGGGA[A/T]TAGCATGCAGTGTTA | 9474 |
rs769968938 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282494 | CTGTGGTTTTTACTG[C/T]ACAATTTTTAATAGC | 9474 |
rs769970602 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265784 | GCAGAAATAAAGAAG[G/T]GCTTTGAAATCAATG | 9474 |
rs769987019 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276480 | AAAAAAAAAAAAAAA[-/T]GAAACTGAAGCTCAA | 9474 |
rs769987926 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302323 | TGGAAAGACCTGGAA[A/G]GAAGTGGGATCATGG | 9474 |
rs770007822 | snp | C/G | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184034 | CGAAGAATAAACACT[C/G]TTAATGTGAACAATC | 9474 |
rs770021837 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266750 | AACCAATGACAAAAA[C/T]CACATGATTCTCTCA | 9474 |
rs770039268 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289352 | AAGACAACCTTTGAA[A/G]TAACCTAGGTCCTGA | 9474 |
rs770041065 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304107 | ACACCTAGAACTAGT[G/T]TGTGAGTTCAGCAAG | 9474 |
rs770049918 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222936 | CTATTATTATTCATC[C/T]AAACTTTACTTTCAT | 9474 |
rs770108738 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297084 | ATCTTAAATTTTCCA[C/T]AGCTCAAGAACTAAT | 9474 |
rs770120876 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262167 | AACCTCCGCCTCCCA[A/G]GTTCAAGTGATTCTC | 9474 |
rs770142838 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322570 | TCTCTCTCAGCTAAT[A/G]ACCTTGCTTTCTATT | 9474 |
rs770143894 | snp | C/G | 1.65814e-05 | 0.00287931 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186617 | CACTCAGCCACTGCA[C/G]AGGTGTTTCCAACAT | 9474 |
rs770171352 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188645 | TGTACAACAGAAGCT[A/G]GAGGACAAAAGCACT | 9474 |
rs770197908 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311386 | TTCACGGGAGGCCTT[C/G]ACACGAAGTGTATCT | 9474 |
rs770272292 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243531 | AGACCCTCTCTGGGG[-/A]AAAAAAAAAAAAAAA | 9474 |
rs770274468 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316201 | AGCACATCTTTGTCA[C/T]CTGTCATTCTTCCAG | 9474 |
rs770290102 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216960 | CAAGTAAGCTGTTAT[-/T]TAAAAAAAAAAAAGT | 9474 |
rs770316811 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309270 | TATTCAAGGTGATAT[C/G]TTTTGACTAATAAAT | 9474 |
rs770322417 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270741 | AAACTTTTAGCCTCC[A/G]AGATGGCCTCTCAAA | 9474 |
rs770323924 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242357 | GAAATAAGCCTGTCA[C/G]AAAAAGGCAATTAGT | 9474 |
rs770366930 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282982 | TTTTTGTAGAGATGA[A/G]GTCTCCCTATGTCGC | 9474 |
rs770376220 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188095 | TAGTGTTAATATAAT[A/G]ATTTGTTTTCATAAT | 9474 |
rs770381471 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291265 | AATAATTAATACTTT[C/G]TACTACTACATCCAG | 9474 |
rs770421964 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213890 | TTTTCATTCCTCTCT[A/T]GAACCATTGTGAAAC | 9474 |
rs770431122 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216502 | CAGACACAAAAGGCC[A/G]TATATTACATGATGC | 9474 |
rs770465471 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229784 | CCCAAATGCATTCAA[A/T]CTGTAGCGGCAACTG | 9474 |
rs770499107 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250369 | GCAGTATATTAGAAA[C/T]GGTGTGAGAGAAAAT | 9474 |
rs770499742 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184328 | AGTCAAATAGGCATA[C/T]TGGGGGTCTTCTCCA | 9474 |
rs770519901 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273754 | TATTCTACTATAAGC[-/T]AGAAGTAGTAAAAAC | 9474 |
rs770563491 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318612 | ATTGTTGCTTACATG[A/T]ATATTTTTTGCAAGA | 9474 |
rs770582219 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287577 | AACCAAAACGCACCA[A/T]ATCAGCACCATGTTA | 9474 |
rs770585726 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190125 | AACTATCCCAATAAT[A/G]TATTTTTCTTCAATC | 9474 |
rs770591941 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197690 | CATGTGACCACCGCA[C/G]ACACCAACTTCCCTT | 9474 |
rs770592938 | snp | C/T | 1.79165e-05 | 0.00299298 | intron-variant | ATG5 | GRCh38.p7 | 6:106279652 | AAAATTAAACACTAT[C/T]ATACTTACCATTTTG | 9474 |
rs770643249 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196675 | TTGCAGTGAGCTGAG[A/G]TGGCATCACTGCACT | 9474 |
rs770717977 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204255 | ATAAATAAAAATAAG[C/T]AGAAAAAATAAACAT | 9474 |
rs770721745 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294075 | ACTTCCTTTGAGTGT[C/T]ACGTCAGTGCTCAAA | 9474 |
rs770723074 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225334 | GTTATCGGAAAACCT[-/AC]ATGTAGATAAAAATT | 9474 |
rs770730815 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106325193 | CTGCACTGTGCAATA[A/G]AGGTTTAAATAACTG | 9474 |
rs770788265 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248925 | CCTGGGCAACAAGAG[A/C]GAAACTCCGTCTCAA | 9474 |
rs770792932 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296805 | CCTAGGCAACAGAGG[G/T]AGACTTGGTCTCAGA | 9474 |
rs770885692 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206594 | GGCAGAGGTTGCAGT[C/G]AATCAAGATCATGCC | 9474 |
rs770904592 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295328 | GACTTAACATTTCAA[A/G]AGTGACACCATATTG | 9474 |
rs770936259 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244384 | AGAAAACTCGTTAAT[A/G]TGGCCTGACTTTTAC | 9474 |
rs771009900 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304305 | TTATAAAAATAAAAA[A/G]TAAAGGAACATTCAG | 9474 |
rs771019542 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247567 | TCGCTCCTGGGGGAA[C/T]ACAAGGTTATGTTTC | 9474 |
rs771025160 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202723 | CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 9474 |
rs771061150 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291352 | TGACAACTAGTACAG[C/T]GAGGTACAATGCCCT | 9474 |
rs771112479 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213897 | TCCTCTCTTGAACCA[C/T]TGTGAAACGTAGAAC | 9474 |
rs771172234 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205029 | AAATAGCCATCCCTC[-/A]ACTCAGGGTTTTTGA | 9474 |
rs771209299 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282694 | ATTCCTAAGCTTGCT[A/G]TAAGTTTTGATGACA | 9474 |
rs771210776 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285146 | TGGGTAACTTCTATC[C/G]ATCTGTCTTTGAGTT | 9474 |
rs771245217 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265060 | GCAAACTGGATAAAG[C/T]GTCAAGACCCATCAG | 9474 |
rs771253921 | snp | C/T | 4.97385e-05 | 0.00498666 | intron-variant | ATG5 | GRCh38.p7 | 6:106292990 | TCTATTTATTATGTA[C/T]CACAAATGGGACGAA | 9474 |
rs771275934 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323522 | GGTATTACAAGCATG[A/C]GCCATCACGCCCGGC | 9474 |
rs771279434 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298475 | AGAATTGCTTGAACC[A/C]GGGAGGCGGAGGTTG | 9474 |
rs771332413 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299544 | GCATAAGAACAGTAT[G/T]AGGTCTATTTTTACA | 9474 |
rs771390259 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231817 | GAGATCAGGATGAGC[A/C]GGCAGAATGGGACAA | 9474 |
rs771397849 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | ATG5 | GRCh38.p7 | 6:106201943 | AACAGAAAATGAAAG[A/G]AATGTTTTAATGTTG | 9474 |
rs771417474 | in-del | -/AACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297760 | ACACACACACACACA[-/AACA]CACACATATATATTT | 9474 |
rs771513716 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220160 | CTAAGCTGAGAATTA[C/T]ATTTTAATATACCAT | 9474 |
rs771529044 | snp | G/T | 3.30115e-05 | 0.00406259 | intron-variant | ATG5 | GRCh38.p7 | 6:106201950 | AATGAAAGAAATGTT[G/T]TAATGTTGCTGATTG | 9474 |
rs771536318 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278294 | ATAGTTTGAAGAGTG[C/T]TTGCTTTCTCAACAT | 9474 |
rs771541572 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243527 | AGCAAGACCCTCTCT[-/G]GGGAAAAAAAAAAAA | 9474 |
rs771615286 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228198 | CACTCTATTAAATCT[C/T]GCAACTGCACTCTTC | 9474 |
rs771645590 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273534 | AGGCATTACCACCTT[C/T]GTATTTGTAATAAAA | 9474 |
rs771668824 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296492 | TCTTATGTGTTGCCT[-/A]AAGTATTGAAACATC | 9474 |
rs771704065 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308846 | TTAAAATGATTCATC[G/T]GAGTCAATTAAACTG | 9474 |
rs771735308 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273133 | TTCAATGAGAAAAAA[C/G]GTTCAAGAAGAGTAG | 9474 |
rs771755405 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295486 | GCCATTAACAAATGT[A/G]TGAAACACTTTTGTG | 9474 |
rs771779864 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185383 | CACAAGAAATGAAAT[C/G]TAATGCACAAATATG | 9474 |
rs771803817 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228844 | GGAAGGGCTTTCTAA[C/G]AACCCTCAACCCTTC | 9474 |
rs771809498 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238933 | AAAGTGGAGGGGGGG[-/A]AACCCAATAACTTCA | 9474 |
rs771851585 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315066 | ATGCTGAGGATGCAC[A/G]GAGGAAAACAAAAAC | 9474 |
rs771870556 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | ATG5 | GRCh38.p7 | 6:106279843 | CAAAGGAAAAAATAT[A/G]CATATAAAACAGGAT | 9474 |
rs771897315 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256828 | AGGCCTAGGACATTA[C/T]TATACTCTACTGTAG | 9474 |
rs771930453 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194443 | TCATGTCTGAAAAAA[A/G]TTTATCTTGTCAACT | 9474 |
rs771935517 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206501 | TAAAAATACAGAAAA[G/T]TAGCTGGGCATAGTT | 9474 |
rs771939342 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224327 | AATAGTTCATCTAGA[A/T]GATAAAGGACCCATG | 9474 |
rs771950704 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254045 | TTACTAAGTTACTAC[C/G]TACCTTACTTACTAA | 9474 |
rs771955786 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296451 | GCCTAGAAGGATGAT[-/A]AGAAGAATGTACCCT | 9474 |
rs771957979 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211886 | ATTCATCAGCTACTT[-/TG]TGTGTGTGCTTTGTT | 9474 |
rs771973524 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267030 | GAGAAAAAATAAAGG[A/G]TATTCAAATAGGAAG | 9474 |
rs771994475 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225432 | GTTCTTAAGCAATAT[A/G]CTGAGTTGAAATTTT | 9474 |
rs772052011 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269486 | GGAGGCTTGGCCGCA[C/G]AGGAGCCCATGGAAG | 9474 |
rs772063313 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282594 | ATCTTAGTTTGGTAA[A/C]ACATTCGATAAACCA | 9474 |
rs772084566 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232029 | ACCTCGTGTCAAGGG[A/T]ATCACTGTAAGGCCC | 9474 |
rs772088626 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293457 | TGTAAATTTATTTAA[-/AT]ATGTTTTTTACTTTT | 9474 |
rs772104154 | snp | C/T | 1.66682e-05 | 0.00288684 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279693 | CAGAGTTGCTTGTGA[C/T]CTTTTTTCTGCATTT | 9474 |
rs772162759 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257879 | GCATGCTCAAACAAG[C/T]TTTTATTTTGTAGGA | 9474 |
rs772176188 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234745 | CCTTTTGTTATCGGA[C/G]CAGGAGTGCTAGGTG | 9474 |
rs772189484 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193844 | GCCCCATAGTACCTG[A/T]TTCAATGAAAAGATA | 9474 |
rs772201627 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278398 | AATATTTTATTATTT[C/G]TATTTCAATGTCATA | 9474 |
rs772272390 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323884 | GGCCCCATTTCCACC[C/T]AAGTATCCACTACTT | 9474 |
rs772272711 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242084 | TATACAATGGAATAT[G/T]ATTAAGCCTTTAAAA | 9474 |
rs772289563 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312208 | TAAGTCTGAGAGACA[-/CT]GAGGTCTCTGGAGTA | 9474 |
rs772308915 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203927 | TGGTTTAAAAAGAAA[C/T]AGACATGGATGAAGC | 9474 |
rs772313582 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246294 | CAGGTTTTGTCAAGC[A/G]AATTTTGAGAATTCT | 9474 |
rs772319681 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231060 | CGGTCCAAAAGGAGA[C/T]AGACAAAGGGGTAAA | 9474 |
rs772342041 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301645 | ATCCAAAATCTGAAC[C/G]TTTTTTAACACTGAC | 9474 |
rs772345501 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220055 | ACCATTGAGAAGTAC[A/G]TACTGTTGAAGACAG | 9474 |
rs772347117 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318831 | GCTTACCTATAATAA[A/G]TTATATAAGAAAGCA | 9474 |
rs772357434 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293732 | ATTTAAAAAAATAAG[C/T]TCCAAAATAAGAGAA | 9474 |
rs772360169 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202752 | CTGCAACCTCTACTT[C/T]CCAGGTTCAAGTGAT | 9474 |
rs772376226 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279541 | CTGTGCAAATCTGGG[-/CA]CAGAGGCTACAATTT | 9474 |
rs772417793 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313650 | TCAGTGATAAACATA[C/T]AGGATATAGGCGGAA | 9474 |
rs772463073 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300648 | CCTAATGTTCCTAGG[A/C]TATAATCCTGTACAT | 9474 |
rs772499685 | snp | A/G | 1.66653e-05 | 0.00288658 | intron-variant | ATG5 | GRCh38.p7 | 6:106293123 | TAAAAATGAAACAGT[A/G]TATTTTGAGAAAATA | 9474 |
rs772499856 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229393 | GACAGAGAGAAAGAG[A/T]CAGTGAGAGACAGAC | 9474 |
rs772507685 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253758 | TTTCTAATGGGCCAT[A/G]AAACATAATGCTTTA | 9474 |
rs772526344 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200497 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 9474 |
rs772544956 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313836 | TAGCCATCACTGATG[C/T]TTTATATATTTTCTT | 9474 |
rs772548847 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197981 | GAGGTTTATGGGGTT[C/T]ATCTCTATCAGCAAT | 9474 |
rs772574262 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286622 | TAACTCAAAGAATGC[A/G]GCAAAGGTGATGGGA | 9474 |
rs772578622 | snp | G/T | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202075 | CTTCTGAATGAAAGG[G/T]CTTTCAGTCGTTGTC | 9474 |
rs772581334 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187077 | GTCGGTCCATACATA[-/TT]TTGAAAATGTAAAAT | 9474 |
rs772601706 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196859 | ACTAGAAATTGGCAA[C/T]CATGAAATAAAAATG | 9474 |
rs772609428 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270931 | TAAAATAAGCCCCAA[A/C]TTTACTGACTTTTCT | 9474 |
rs772621176 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222468 | GTTTCAATCTCTTCA[C/T]ATTAAGGGGAGAACA | 9474 |
rs772631177 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221484 | TGAGCCCAGGAATTC[A/G]AGACCAACCTGGGCA | 9474 |
rs772658835 | snp | G/T | 1.66446e-05 | 0.00288479 | intron-variant | ATG5 | GRCh38.p7 | 6:106316067 | AAAAATGGACAAGGT[G/T]AAATATCCCATTTGC | 9474 |
rs772682612 | snp | A/T | 1.65031e-05 | 0.00287251 | utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316220 | TCATTCTTCCAGGAG[A/T]TAAAGCAGTACATAC | 9474 |
rs772687498 | snp | A/C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264099 | CTAAGAATCTTGATA[A/C/G]AAGGTTATAGGAAAT | 9474 |
rs772688299 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209898 | GAGCTTTGTTAATCA[A/G]AGTTTTCTCTGAGGA | 9474 |
rs772736562 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252832 | TAAGAAGCCAAGGGA[C/G]AGCAGAGTTACAGCA | 9474 |
rs772774070 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268309 | TCATTAGAGAAATGC[-/A]AATCAAAACCACAAT | 9474 |
rs772777225 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316313 | CCTTGCAACGATGAA[C/T]GAACCTGCTAGAAAA | 9474 |
rs772793344 | snp | A/C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308210 | AAATATTTTCAATAA[A/C/T]GTATTCTAGTAATAG | 9474 |
rs772796615 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306588 | AATGTCAGTAGTGAC[C/T]CTATTGAGAAATCCT | 9474 |
rs772826506 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268535 | TACTGAGTATATTCC[C/T]AAAGGATTATAAATC | 9474 |
rs772858603 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106238142 | CTTGTCTTTACATAT[C/G]AGATACAAATCATAT | 9474 |
rs772876005 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270726 | CTCATTAGACATCTC[A/C]AACTTTTAGCCTCCA | 9474 |
rs772879244 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193056 | CGCTGATTTTAAAAG[A/G]GCAATTAATCTTGGA | 9474 |
rs772881483 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246447 | CCTTTCTCTCTCTCT[C/G]TCTCTGAAACTTATC | 9474 |
rs772940856 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194771 | CTAACTCCTGACCTC[A/G]GGTGATCCACCCGCC | 9474 |
rs772948319 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204176 | GCACATGCATATCTA[C/T]GTAACAAACCTGCAC | 9474 |
rs772971691 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278578 | CATAATCTAGTCTCT[C/T]GAAGGGCAGCCATGT | 9474 |
rs773006939 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302050 | CATGACAAGAATATA[-/G]GAAGTACACACGTAG | 9474 |
rs773012502 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279517 | GTAAGGGATGACTAA[A/G]AGTAGCTTCTGTGCA | 9474 |
rs773046276 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216383 | AATTGATAAACAAAA[C/T]GTGGTATCTTCATAC | 9474 |
rs773077175 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307276 | AGTCCATTTTTAACC[A/T]ATTTGTATTTTTCAT | 9474 |
rs773145244 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244890 | AAAAACAGATATGAT[A/G]TGCTTAATTTTCATT | 9474 |
rs773146672 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215341 | GTGGAGCTCTTCAAA[C/G]AGTCTCACCTACCCT | 9474 |
rs773152101 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312916 | AGGCAGAGAATGACT[A/G]TAAGCAACCTTTTTA | 9474 |
rs773158138 | snp | A/G | 1.65403e-05 | 0.00287574 | intron-variant | ATG5 | GRCh38.p7 | 6:106202117 | GGAAAAAATGATTCA[A/G]GCAATTAAGTCTTTG | 9474 |
rs773171568 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215316 | GATTCTAAACCTGGG[C/G]TAGGAGCTAGTGGAG | 9474 |
rs773179596 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203012 | ACAGAGAGAGAGAGA[A/C]AGAGAGAGACAGAGA | 9474 |
rs773203018 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292722 | TCCTGGGCTCACCTC[A/G]GCCTCCCAAAGTGCT | 9474 |
rs773207210 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190167 | CCAGGACTGTCTTAG[A/T]CTGTCTGTGATGCTA | 9474 |
rs773223734 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258052 | GGAAGCCAAATTGAC[A/G]CAAGTTATCACAATT | 9474 |
rs773274651 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106325652 | CGGGGACGCGGTAGC[A/C]GGACTCCAGGAAGCC | 9474 |
rs773280451 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255635 | ACCAATTAAGAATAA[C/T]TTATTTCAAATGTAT | 9474 |
rs773296944 | snp | G/T | 1.65877e-05 | 0.00287986 | intron-variant | ATG5 | GRCh38.p7 | 6:106292980 | CTACTCGAAGTCTAT[G/T]TATTATGTATCACAA | 9474 |
rs773335300 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195347 | ATCTTAAAGTCTTTC[A/G]CTTTCAACTTAAGTT | 9474 |
rs773339871 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241520 | ATAACTGAAAACAGG[G/T]TGTACACCCATTTCA | 9474 |
rs773348478 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199862 | CATTTACCCTAGCAC[G/T]AGAGATACATGGATG | 9474 |
rs773368854 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254217 | CCTCAGAAAGATTTC[C/T]TTCATAATCCTAGGT | 9474 |
rs773369099 | snp | G/T | 1.65531e-05 | 0.00287686 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106279719 | CATTTCATTGATTAC[G/T]TGACTTTTATGTTTT | 9474 |
rs773380710 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207329 | GCAGAAAAACGAAAC[-/TT]TTATAAACATTTTAG | 9474 |
rs773392698 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229179 | ATTTCCTCTAGCAAG[C/T]TGTATCTCCAAAGGG | 9474 |
rs773427639 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193900 | CTATTATTTTGGTAA[A/G]AGAATTTTGTTTTCT | 9474 |
rs773459851 | snp | A/G | 1.65844e-05 | 0.00287957 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186622 | AGCCACTGCAGAGGT[A/G]TTTCCAACATTGGCT | 9474 |
rs773459917 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298447 | TCCCAGCTACTTGGG[A/G]GGCTGAAGTGGGAGA | 9474 |
rs773503409 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212451 | TTCGAGATCAGCCTG[A/G]CCAATATGGTGAACC | 9474 |
rs773520172 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311393 | GAGGCCTTGACACGA[A/C]GTGTATCTTAAGGCA | 9474 |
rs773549759 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264766 | TAAGCGAAGGAGAAA[C/T]AGAATCCTTTAGAGA | 9474 |
rs773577288 | in-del | -/AGC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262716 | TGGAGGGTGACCAGA[-/AGC]AGGGTGGGGCATTCC | 9474 |
rs773611405 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262173 | CGCCTCCCAGGTTCA[A/C]GTGATTCTCCTGCCT | 9474 |
rs773668973 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251049 | ACCAGCCCTCAAGAC[A/G]GAATCTAGCACTCCA | 9474 |
rs773673265 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188901 | TATCTCACCGGCATT[A/T]ATGTATTTTGTTTAT | 9474 |
rs773733738 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317427 | CCTCTTCCACTGACC[A/G]ATGACATTAAGATGG | 9474 |
rs773747121 | in-del | -/GACA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297758 | ACACACACACACACA[-/GACA]CACACACATATATAT | 9474 |
rs773774997 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106293959 | TAGAGAAGTGTTTCA[G/T]ATTTCAGCTTTTTTT | 9474 |
rs773784535 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275462 | GTGTAAGCTTATTCA[C/T]AATCATCACAAATAA | 9474 |
rs773829024 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230170 | GCAGAGTTAGAAAAA[C/T]TGCCTAATAATTGGT | 9474 |
rs773836998 | snp | A/T | 1.66366e-05 | 0.0028841 | missense, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186660 | ATGAATCATCACTTG[A/T]TTCTTTTTTTCCCCA | 9474 |
rs773838013 | snp | C/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184329 | GTCAAATAGGCATAT[C/T]GGGGGTCTTCTCCAA | 9474 |
rs773868205 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219426 | CCTCCCTATCCAGGG[G/T]TTCTGCATCTGCAGA | 9474 |
rs773918955 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206990 | AGGTTGACAGACAAG[-/A]AAAGCCACTGCAAAC | 9474 |
rs773956267 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307464 | GAACAAAACTCCCAA[C/T]AACAGAGGAAGCACC | 9474 |
rs773967174 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185336 | TAGCGTACTCAAATG[G/T]GTCAACATTCAATAT | 9474 |
rs773987090 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217777 | TATTTACAATGTAAG[A/T]ACCTATTTCCACAAA | 9474 |
rs774005583 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277119 | ATGCATGCCTTACTT[G/T]CTCTTGATACCACAG | 9474 |
rs774012853 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266189 | GATCTCACAAAAATA[C/T]AAACCACCATCAGAG | 9474 |
rs774021980 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251960 | GTTCTCCCACCTCAG[C/T]CTCCCAAGTAGCTGG | 9474 |
rs774047717 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106246727 | TTTCCGGACTCTTTG[G/T]GAAATGTCTTCAGAG | 9474 |
rs774048940 | snp | A/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326249 | GAACCCTCCCACCCA[A/T]CCAAGAGTACATATC | 9474 |
rs774053622 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236108 | TCATAGAGTATGTTC[-/T]CTTTGTATTGGTTCT | 9474 |
rs774096026 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326438 | AAAAATTAGCCGGGC[A/G]CGGTGGCGGGCTTCT | 9474 |
rs774107707 | snp | C/T | 1.67607e-05 | 0.00289483 | intron-variant | ATG5 | GRCh38.p7 | 6:106248251 | CAAATCTGTCTGTAA[C/T]GATATAAATTATTTG | 9474 |
rs774108072 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264574 | ATGAAGGAAAAAATG[C/T]TAAGGGCAGCCAGAG | 9474 |
rs774108932 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267825 | ATTCCTTACACCTTA[A/T]ACAAAAATGAACTCA | 9474 |
rs774111040 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243905 | AAGTAGGAACCATCC[-/TT]TTTTTTTTTTTTTTT | 9474 |
rs774137200 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317762 | AAATTTCCAAGTTTA[A/C]AAATGACACAAAATT | 9474 |
rs774159252 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265806 | AAATCAATGAGAAAA[A/G]AGAGACAACGTACCA | 9474 |
rs774190592 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318721 | CAAACTCTGCAAAAC[A/G]GATTTATGAAAACTG | 9474 |
rs774201130 | snp | C/T | 1.78618e-05 | 0.00298841 | intron-variant | ATG5 | GRCh38.p7 | 6:106279654 | AATTAAACACTATTA[C/T]ACTTACCATTTTGCA | 9474 |
rs774221741 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295385 | AACACAAAGAACTCC[A/G]CTAGGCAAAATAGTC | 9474 |
rs774223829 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228614 | ACCATCTTCGGAGTT[C/T]TGGGAGCAAGGACCC | 9474 |
rs774304985 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253966 | GATTCCTACCAGGCC[A/C]ATTCCACCCCCTTGG | 9474 |
rs774310106 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311592 | AGATGCTGAATATGA[C/T]AGGAAGGTACAGAGT | 9474 |
rs774342357 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234676 | ATTTACACTGAACAA[G/T]ATTTATACAATTATG | 9474 |
rs774370596 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204353 | TAGTAATCCAATAAT[A/G]TATTTGAGTGTTTGT | 9474 |
rs774377298 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247603 | GCCCTCGGTCACAAC[A/G]TGTTCATTAACTGAT | 9474 |
rs774432169 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233531 | AGTCCTTACACAGGT[C/T]GATGAGCTTGCAACC | 9474 |
rs774463851 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200018 | TCCTTCAATCCTTTC[C/T]GGCATTGGTTCTGAC | 9474 |
rs774477893 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189043 | AGCATGGTACCTGAC[A/T]TATACAGTAATTAGA | 9474 |
rs774494595 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237374 | CTAAAACCTCAATAA[A/G]CATATTCATCTTCTT | 9474 |
rs774504233 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242902 | ATTTCTTATCAACAT[C/T]GCTAAAACCCTGGAG | 9474 |
rs774510297 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256815 | TGAGTGAATGTGAAG[A/G]CCTAGGACATTACTA | 9474 |
rs774543866 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287119 | TTTATAGCTGGGAAG[C/T]GCAGGCAGTGATAGA | 9474 |
rs774552148 | snp | A/T | 1.6569e-05 | 0.00287824 | intron-variant | ATG5 | GRCh38.p7 | 6:106292995 | TTATTATGTATCACA[A/T]ATGGGACGAAGGAGA | 9474 |
rs774553021 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106275968 | CGGGTTCCAGTAAAT[C/G]TTTATTTACAAAAGC | 9474 |
rs774559454 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244422 | GCCTTATCCAAACTC[G/T]GTGGTCAAGACAAAC | 9474 |
rs774586388 | in-del | -/GAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214975 | AAAATCATACCAAGG[-/GAA]GAAGTATAGTTTAAA | 9474 |
rs774605082 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200934 | CATGAAGGATTGGTT[C/T]AAGGATCCCTGAGGA | 9474 |
rs774637642 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229963 | AAAAAGGTAATTTAA[C/T]ACTAACCACTGATAA | 9474 |
rs774662892 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200276 | GGCAAACTATTTCCT[C/T]AGATGCAAAATGCTT | 9474 |
rs774666006 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285010 | CATTATTTCTTAAAA[A/T]TATTTCTTCTGACCC | 9474 |
rs774689589 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213921 | GTAGAACCAAGAAAG[C/G]TAACAGTATTTAGTT | 9474 |
rs774715569 | in-del | -/G | 1.65135e-05 | 0.00287341 | intron-variant | ATG5 | GRCh38.p7 | 6:106202096 | AGTCGTTGTCTATTT[-/G]AAAAAGGAAAAAATG | 9474 |
rs774728512 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266213 | ATCAGAGAATATTAT[-/A]AACACCTCTATGTAA | 9474 |
rs774730373 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189854 | CCCACTCAGGTTTTT[A/T]AAAAAAGCTAGCTTG | 9474 |
rs774776776 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309713 | AAGATTCAGTGTAGT[C/T]TTTCAGAAATGACAA | 9474 |
rs774850090 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197930 | ACAATACAGAGAAAT[A/G]AGTAACTGAAAGCCA | 9474 |
rs774856887 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247720 | ACTAATAAAAAGCAC[A/G]AAAATGTAAAAGCAT | 9474 |
rs774878245 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287925 | AAAATGTTAAAAAGC[A/G]GCAAATCCAAGTGAA | 9474 |
rs774910858 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205783 | TACTGGGGACAAAGC[C/G]CCAGTGCTATTACAT | 9474 |
rs774915993 | in-del | -/AAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250579 | TCTCACATATGAAGC[-/AAT]TATTCTGTCAATGCT | 9474 |
rs774917998 | in-del | -/TA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303820 | ATACAATCATATAAT[-/TA]TAGCACAGAAAAGGC | 9474 |
rs774918635 | in-del | -/TATT | 3.572e-05 | 0.00422596 | intron-variant | ATG5 | GRCh38.p7 | 6:106308516 | AAATTTGTAAAACCG[-/TATT]TATTTACTAGTTATT | 9474 |
rs774926834 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224988 | ACAAAAGAATACAGG[A/G]GGCATGACAAGCCAT | 9474 |
rs774937065 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200477 | AATACAACTCTGCAA[-/T]TTTTTTTTTTTTTTT | 9474 |
rs774945393 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263045 | AGAGTCAAGTGGTCT[C/T]GCTCAGTGGGTCCCA | 9474 |
rs774947104 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203683 | TGCAACCCCCAAGTT[A/G]CAATCCTCCACCTAA | 9474 |
rs774973597 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285173 | GTTCAAAGAACCTTA[-/C]CTTCTGCCATCTTTA | 9474 |
rs774980032 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208878 | AAAAGACATGAACAG[A/G]CATTTTACCAAAGAG | 9474 |
rs774991153 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312438 | GATCTCCAGCAGACA[A/G]ATATATAGGTTTGGA | 9474 |
rs775002896 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201277 | ATTCAAGTGTATATG[-/TG]TGTGTGTGTGTGTGT | 9474 |
rs775025112 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233811 | TTACTGTTCTCTTAC[C/T]CCCTTTCACTCTCAC | 9474 |
rs775072189 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312249 | CTATCTGGGATAAGA[C/G]AGAAGGAAGGAAGCA | 9474 |
rs775091336 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106281731 | AGTAAGTGTATGTTC[C/T]AACTTTACTTAAAAA | 9474 |
rs775110845 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295505 | AACACTTTTGTGAAT[C/T]TGTAAGCAAATTCTA | 9474 |
rs775112164 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249288 | AGCCCCTGAAAAATC[A/T]CTACTTTCTATCTCT | 9474 |
rs775159649 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289717 | AATAAAACCACTATA[C/T]ATTAACACTAAAATT | 9474 |
rs775160006 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288346 | TGAGATAATTTTCTT[C/G]GTAGTCTCACCAAGT | 9474 |
rs775173371 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216880 | GGGCAACACAGACCA[C/T]GTCTCTAAATAAATA | 9474 |
rs775188634 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233693 | ATCTCATAACGTGAA[C/T]GGCATACTCACTGCT | 9474 |
rs775202380 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188553 | ACAATATGGTAAACA[A/G]TCCACTGATGATGCA | 9474 |
rs775212379 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212894 | TGGTACATTACTTTA[A/G]AGAATCAAGTAGCTG | 9474 |
rs775217637 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315848 | GATTCCATTAACATA[C/G]CCACATACATGTAAG | 9474 |
rs775228707 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282707 | CTATAAGTTTTGATG[A/G]CAAACACGTATTAAA | 9474 |
rs775279595 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273958 | TTAAAATGGCACACT[A/G]TCAAATAATTATTGT | 9474 |
rs775291237 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185391 | ATGAAATGTAATGCA[C/T]AAATATGTTTGACTG | 9474 |
rs775301851 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255839 | ATTTACAGAGCTACA[C/G]CACAGTGGTAGGCCA | 9474 |
rs775304802 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290341 | TTCATTTATTTTTAG[-/A]AGAGAGTTTTGCCCT | 9474 |
rs775368179 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304819 | TGAATTGGCCAGGCA[C/T]GGTGGCTCACACCTG | 9474 |
rs775369552 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248545 | AAAAACACACCAGGT[A/G]GAGGATAGATGTCTT | 9474 |
rs775371511 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194448 | TCTGAAAAAAATTTA[C/T]CTTGTCAACTAATTC | 9474 |
rs775393472 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212124 | AGTAGTACTATGTGT[C/T]ATTTAAGAATTAAAT | 9474 |
rs775419723 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279366 | TGACTAAGGAATAAA[C/G]ACCACATCCTTAGAG | 9474 |
rs775424878 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206509 | CAGAAAATTAGCTGG[C/G]CATAGTTGTGGGCGC | 9474 |
rs775427438 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190530 | TGTCTCTCTACTCTC[-/TT]TTAATCTGCAACCGT | 9474 |
rs775435442 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265895 | CACATCAGAAAGCTC[A/G]AAAGATCTAAAATCG | 9474 |
rs775446192 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299767 | GTATAAATATCTGTA[C/T]TCAGATAGCAAACTA | 9474 |
rs775447130 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315115 | CCAAAAAGTGAGCGA[A/G]TGGGCTCCTTAATAA | 9474 |
rs775488927 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106191176 | TCCAGACTTTCTGAA[C/T]CAATTTCTGGGGTAA | 9474 |
rs775489604 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225544 | CAACAAAATCCATTT[A/C]TCCAAACTTGAGGTT | 9474 |
rs775528222 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234780 | AGGTTCTGGCATTGG[A/C]GGTACCACAACCTCT | 9474 |
rs775579466 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224539 | GTGAATGGAAGTAGA[C/T]TGGTGGGACCAGTTA | 9474 |
rs775593263 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189175 | AGAATAACTCTACCC[A/G]TAAAGACTGTTTTGG | 9474 |
rs775606776 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221498 | CGAGACCAACCTGGG[C/T]AACATGGTGAAACCC | 9474 |
rs775623968 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321649 | AGGCGTGAGCCACCG[C/G]GCCTGGCCAACTCTT | 9474 |
rs775627464 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285598 | AATAGAGATTGGCAA[A/G]CTTTCTGTAAAGGAT | 9474 |
rs775645979 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260483 | CTGTGCGAAGAAATG[C/T]TTCTTAAGTAGAAAA | 9474 |
rs775665337 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276160 | CTAACAGATATTCTC[-/TT]GTTTTATAGATTAAG | 9474 |
rs775694678 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232177 | GGGTATGCTTGACCA[C/T]TGACGGCCAGGAGGC | 9474 |
rs775696733 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220336 | ATTATTACAAACAAT[C/T]TGCATGCACTGCAAA | 9474 |
rs775715285 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278479 | TTGGGACATCTTCAT[C/G]CTTTTGTCACAACTA | 9474 |
rs775730281 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319551 | ATGCTGGTGGTACCC[G/T]TACCCTAAAGCAGCC | 9474 |
rs775749935 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190047 | TATCACAATAAAAAA[C/T]ACTGATATACCATGA | 9474 |
rs775751189 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252230 | TATATATACTTCTCG[A/C]CAGAGCTACAAGCAA | 9474 |
rs775810854 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287656 | CTATTAAACTTTATT[C/T]AGGATTTGCAACAGA | 9474 |
rs775814906 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271152 | AAGGCCTTAGATAAT[C/T]TGGTTCTTTCTCATC | 9474 |
rs775821657 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311913 | TCGGCTCACTGCAAC[A/G]TCTACCTCCCAGGTT | 9474 |
rs775832183 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297309 | GCAAAAGTTCTATTT[A/C]TATAAAAAGAAGACT | 9474 |
rs775832612 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209917 | TTTCTCTGAGGACCT[A/G]TAGCATTTTGGTTAT | 9474 |
rs775845406 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305091 | AGCAAAACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 9474 |
rs775868049 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272323 | GGTCTCCTACCATCC[C/T]ACTCTCTGTTCCTCC | 9474 |
rs775884961 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318880 | TTAACTTTAAAAATA[C/T]GTAAGAAAAATTGGG | 9474 |
rs775905991 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283095 | TGCACCTGGCCTACA[C/T]GGATTGAGATTTGAA | 9474 |
rs775987161 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197984 | GTTTATGGGGTTTAT[C/T]TCTATCAGCAATAAA | 9474 |
rs775987460 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220408 | AATAAAACCAAAAAA[C/G]AGGCATCACACACAA | 9474 |
rs775992466 | snp | C/G | 2.37116e-05 | 0.00344314 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308489 | TACTCTTGGCAAAAG[C/G]AACTGAAATGAAAAT | 9474 |
rs776002218 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234879 | CACCTTGCAAGATCA[A/C]CTTAACTTCCTAGCA | 9474 |
rs776010627 | snp | A/C/G | 6.68375e-05 | 0.00578056 | intron-variant | ATG5 | GRCh38.p7 | 6:106293125 | AAAATGAAACAGTAT[A/C/G]TTTTGAGAAAATAAA | 9474 |
rs776044145 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286697 | TTACTACCAGACTAC[C/G]TCTAGACTTTCTTTG | 9474 |
rs776047549 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241139 | GTCCAGGTGACAGAA[C/T]GAGACTCTGTCTCAA | 9474 |
rs776090474 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252921 | GGAAGGAAAAGCAAA[C/T]GGCTGAAAATCACTA | 9474 |
rs776102074 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225337 | TATCGGAAAACCTAT[A/G]TAGATAAAAATTTCC | 9474 |
rs776103219 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273755 | TATTCTACTATAAGC[A/C]GAAGTAGTAAAAACA | 9474 |
rs776115765 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250733 | ATGGTGCATGCATAG[G/T]ATGTGCTCTTGAATC | 9474 |
rs776118520 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219263 | TCAATTTTCTATATT[C/T]CATGTCATTTCTATT | 9474 |
rs776132455 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300652 | ATGTTCCTAGGCTAT[A/G]ATCCTGTACATCATG | 9474 |
rs776146976 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215714 | GAAATGGTTTCTTAC[-/A]TACGGCAACCTAAAA | 9474 |
rs776190235 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194647 | GGTTCAACCAATTCT[C/G]CTGCCTCAGCCTCCC | 9474 |
rs776190821 | snp | A/G | 1.65201e-05 | 0.00287398 | intron-variant | ATG5 | GRCh38.p7 | 6:106202097 | GTCGTTGTCTATTTG[A/G]AAAAGGAAAAAATGA | 9474 |
rs776192910 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327225 | GTATCTAAAAAATAA[A/G]ATGGATTTAGGGGCG | 9474 |
rs776194755 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286133 | CCTCAGCCAAGCACC[C/T]AGGGAGAACATACAC | 9474 |
rs776195549 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245234 | TGACTATAGTCATTT[C/T]GAGCTCATGATAAAT | 9474 |
rs776216313 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106316058 | TTTTCTTACAAAAAT[G/T]GACAAGGTTAAATAT | 9474 |
rs776254921 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235667 | GTAAAAAAATAGCCA[A/G]TCATCTATCGCCTGA | 9474 |
rs776260061 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291639 | GCTTATTTTTCACAC[A/G]CAAAAAAATCTAATT | 9474 |
rs776271765 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306744 | TGCTACTCTCCCACA[-/CT]GTTTCCCCGTCCATC | 9474 |
rs776286566 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256954 | TTTGAGTCTTTTGTA[A/G]TAACACTTAGCTTAA | 9474 |
rs776315646 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284602 | TCAAGTGATACAACT[A/G]CCTCATCCCCACAAA | 9474 |
rs776318438 | in-del | -/A/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221711 | AAAAAAGAAAGAAAG[-/A/AA]AAAAAAAAATCAAAA | 9474 |
rs776332241 | in-del | -/TTAT | 1.70194e-05 | 0.00291709 | intron-variant | ATG5 | GRCh38.p7 | 6:106248260 | CTGTAATGATATAAA[-/TTAT]TTGTTATTAAAAATG | 9474 |
rs776373591 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185517 | AGAAAAGGTACTGCA[C/G]TCAAGAGACAGGTAA | 9474 |
rs776375196 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205813 | TAGTGTAGCTAAACG[C/T]TGTAGAATGGTAAAA | 9474 |
rs776382597 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106306527 | GCTGTTAAACATCCT[A/G]TAATGTACAGGGTAG | 9474 |
rs776393171 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312209 | AAGTCTGAGAGACAC[A/T]GAGGTCTCTGGAGTA | 9474 |
rs776436407 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292441 | AGTCTGGTCTTAAAA[A/T]CTACAGGAATGAACA | 9474 |
rs776447176 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226794 | GAGTTACAAAAAAGT[A/G]CCAAACAAAAATTCT | 9474 |
rs776478438 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106201991 | AGGATCAATAGCAGA[A/G]GGACAAACTTCTTTG | 9474 |
rs776541688 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106232854 | TGGACCTTAAGGATG[C/G]CTTTTTCTGCATCCC | 9474 |
rs776559034 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265738 | ATGAAAACCGCTCCT[A/G]AATAACTACTTGGTA | 9474 |
rs776571681 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211740 | AAATCCCTGTAAACT[G/T]AATGCATAATATCAT | 9474 |
rs776573687 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256031 | AATTTAATATGCAAT[C/T]GAGTTCATTTTTACT | 9474 |
rs776596214 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106225837 | GGCAATTGTTAAACA[C/T]CACATCTGCCATGAG | 9474 |
rs776599871 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287779 | CTCAACATGGACAAA[A/G]AGAGAAAAAATTTTT | 9474 |
rs776631522 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234906 | AGCATCAGTAGTCCT[C/T]CAAAATTGAAGAGCT | 9474 |
rs776635935 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106215221 | AAGAAGAAATGTCTG[A/T]GTAAAAGCAGCTGTG | 9474 |
rs776654081 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106268292 | AAGCTCATCTTCACT[G/T]ATCATTAGAGAAATG | 9474 |
rs776656759 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106220192 | AGCAATCTGCAAAAG[A/C]AGCAACTTGCCTAAA | 9474 |
rs776686859 | in-del | -/A | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326455 | GTGGCGGGCTTCTGT[-/A]AGTCCCAGCTACTGG | 9474 |
rs776726997 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214026 | GAGAATAAATATTAT[A/G]TGGCACAAAGAAAAA | 9474 |
rs776758953 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211561 | TAAAAATAAAAAAAA[C/T]TAGCCGGGAGTGGTG | 9474 |
rs776760252 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106253085 | AAATATAGACCCATA[C/T]GAATTAATTTCTTCA | 9474 |
rs776814810 | in-del | -/TT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106315659 | AAGCTATAAAAACAC[-/TT]TTAACAAACAGTTGC | 9474 |
rs776823875 | in-del | -/CT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106283769 | GTGCAGGGTGTTTTA[-/CT]CTCTGAGGCTTTTAA | 9474 |
rs776846584 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264533 | CAACCCCAAGACACA[C/T]AATCATCAGATTCTC | 9474 |
rs776853560 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210081 | TAACCTTTCAACCTA[C/T]TCTAACACACTTGAA | 9474 |
rs776853660 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106222778 | AGCAAGTTTCAATGA[C/T]CAATCTTTTTCTCAA | 9474 |
rs776861976 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310064 | AATAAAATATTTTTT[A/T]CAATAAGGAAAAAAG | 9474 |
rs776866416 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267509 | ATTTCATATGGAACC[-/A]AAAAAAGAGCCTGTA | 9474 |
rs776884700 | in-del | -/AAAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251708 | GAAAAAGAAAGAGAA[-/AAAG]AAAGAAAGAAAGAGA | 9474 |
rs776937873 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106272416 | TGCCTGACTTCCAGT[C/T]TGACCTCCTTACCAC | 9474 |
rs776956806 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257541 | CTGTTGACTGAAACA[C/T]CATAATGCAGAGCAT | 9474 |
rs776967697 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260152 | TTAGGAGAAATATCC[A/C]ATGTAAATGACAAGT | 9474 |
rs777008970 | snp | C/T | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326109 | GGCATCACACAACAG[C/T]ATTAATAAAACATTA | 9474 |
rs777010932 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261146 | AAATATGCAGAGATA[C/G]ATCAAGTGAGCTAGA | 9474 |
rs777016464 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308959 | AAGGCTGAGAGAGAA[A/T]GCTGAGCTAGGTAAA | 9474 |
rs777045028 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265293 | GGATCAATGCAACAA[-/C]AAGAGCTAACTATCC | 9474 |
rs777067730 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295765 | GATAGTGTCCAACTA[C/T]GTTGCCCAGGCTGGT | 9474 |
rs777071997 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218224 | CCAGGTCTTAAAAGA[C/T]GATAAACATGGCCTC | 9474 |
rs777112746 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187038 | ACTGTAATATATGGT[C/T]ATTAAAAATGACAAG | 9474 |
rs777121453 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234584 | ATATTTTTTGTCTGT[A/G]GTACCTTAGCCTATC | 9474 |
rs777144954 | snp | A/G | 1.67262e-05 | 0.00289185 | intron-variant | ATG5 | GRCh38.p7 | 6:106316052 | ACAGCTTTTTCTTAC[A/G]AAAATGGACAAGGTT | 9474 |
rs777164794 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318545 | TTCTACAGTAGGATT[C/T]TAAGTACAAAAACTA | 9474 |
rs777165607 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199689 | ATTTAACTAAAACTC[C/T]TATTGAAAGCTAAAA | 9474 |
rs777230348 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241445 | TATGGCCATTCCTCA[A/G]GAAAATAAAAATAAA | 9474 |
rs777285883 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228979 | CATTAGCCGGTTGAG[A/T]TCATGTCGCAGCCAG | 9474 |
rs777310833 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286149 | AGGGAGAACATACAC[A/G]TACACTTTGGCTCCT | 9474 |
rs777357772 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210984 | AATAACATATACTAT[G/T]CTTGTAGTCAACCCT | 9474 |
rs777395784 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236193 | CCTTTTAATCCTGAA[G/T]AGTATGCTGTTTTAG | 9474 |
rs777424212 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190075 | TGATATATAAAATAA[C/T]AAAATATTCATTGTA | 9474 |
rs777437168 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106263767 | TGCAGAAGAGGGGCC[C/T]TAACAAAAAGAAAAT | 9474 |
rs777483230 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252745 | CAATTCAGCTGGCTA[G/T]GACCCTCATGCAGGA | 9474 |
rs777509651 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271728 | CAACTGCCAAAAAAA[C/T]GCTTTGCATCCCACA | 9474 |
rs777526050 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185240 | ATCTCACTTCAGCAT[C/T]TGTATAATTTTTTAT | 9474 |
rs777544995 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106299432 | TGCAGAACCCATGGA[C/T]ACAGAACACCAACTC | 9474 |
rs777557377 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307326 | AGCCTGTATTTTTTT[-/C]CATTCAACTGTATCC | 9474 |
rs777579046 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197542 | GTGGGGGGGGCGGGG[A/G]TGGATCCCTCATGAA | 9474 |
rs777596224 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221811 | TGAAATCATAAAAAG[G/T]TGAGGATGAGAAAGA | 9474 |
rs777598324 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209593 | ATCCTTCTGTTGAAA[C/T]GGGTATATTTTGAAT | 9474 |
rs777618977 | snp | A/G | 9.43637e-05 | 0.00686825 | intron-variant | ATG5 | GRCh38.p7 | 6:106279629 | CATATTTTATAAAGT[A/G]GTATTCTAAAATTAA | 9474 |
rs777652167 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106240848 | GATTAAACATAATGC[A/G]GCCATTAAAAAAGAA | 9474 |
rs777675536 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247530 | GTTCTGTTCTATAAG[A/G]TTACCACAAACACTG | 9474 |
rs777681389 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106304126 | GAGTTCAGCAAGGTT[A/G]CAGAACACAAAAATC | 9474 |
rs777695555 | in-del | -/AT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295078 | TACACACACACACAC[-/AT]ATACACACATATATA | 9474 |
rs777702907 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259546 | GTAAAGCATTTCCCC[C/T]TTCAACAAGTCCATG | 9474 |
rs777755827 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106260701 | TAAAAGGATTCTGAA[C/T]GTTACATAGCTTCTA | 9474 |
rs777790672 | in-del | -/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184092 | TATAAGTCAGTGGAT[-/T]TTTTTTATCCTTACA | 9474 |
rs777801849 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284162 | TTTCCCTATTTTGCA[C/T]ATCAGAATTACATAT | 9474 |
rs777816050 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106195150 | ACTCCACAAGAACAA[C/T]GACCTAAAGCACGTA | 9474 |
rs777839261 | snp | A/C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226526 | GTTATTTTAAATATG[A/C/T]GCAAAGAACTAAAAA | 9474 |
rs777867283 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106207997 | CTCGGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA | 9474 |
rs777874618 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247178 | AAAATGGCTACAAAG[-/A]AAAGTTATGACAAAA | 9474 |
rs777883198 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256703 | AAGGTACAGTAAAAA[C/T]ACCATATAAAATATT | 9474 |
rs777887909 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316962 | CAAATCCCTACTCTG[C/G]AAACCATGCTCACAG | 9474 |
rs777898330 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202043 | AACTGTCCATCTGCA[A/G]CCACAGGACGAAACA | 9474 |
rs777910200 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243677 | CTCTACTAAAAATAC[-/A]AAAATTAGCCAGGCA | 9474 |
rs777916313 | in-del | -/CC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228733 | GCTACTCTGGCCTAT[-/CC]CTTAGAATTGGAGGA | 9474 |
rs777953826 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106323471 | GTAGAGACAGGGTCT[C/T]GTTATGTCGCCCAGG | 9474 |
rs777972007 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252839 | CCAAGGGAGAGCAGA[A/G]TTACAGCATTTCAAA | 9474 |
rs777999946 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221490 | CAGGAATTCGAGACC[A/G]ACCTGGGCAACATGG | 9474 |
rs778035680 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262924 | ACTGGGCAGCCATTT[C/G]GGCAGACACCGAGCT | 9474 |
rs778062354 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231779 | AACCCTATTGAACTT[C/G]GCAACCTCAGTTTTT | 9474 |
rs778064794 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194375 | CCAAATACTTAAAAG[C/T]ATCTGCTTTATACGG | 9474 |
rs778110377 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235334 | CGGCCTACTAGCCCA[A/T]GCTCCAATTGTAATG | 9474 |
rs778118914 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312343 | AAATAATGCAGAGGA[C/G]CAGATTTTTTTGGGG | 9474 |
rs778152595 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106245913 | CAACAGAAATCTGAT[A/G]TTGCCTTTAGATCAC | 9474 |
rs778162327 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189729 | GTAAACAATATTTTT[C/G]GTAAACATGTCTTTT | 9474 |
rs778163526 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106236746 | GAATGAAAAATTAAA[C/T]ACAGTGGAGACATTT | 9474 |
rs778164072 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203657 | CTGTCACCCAGGTTG[A/G]ATTGCAGTGGTGCAA | 9474 |
rs778180207 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106307097 | TCTACTCATTCTTGG[A/G]ATCTCATCAGCACAA | 9474 |
rs778187845 | snp | A/C | 0.000102356 | 0.00715314 | intron-variant | ATG5 | GRCh38.p7 | 6:106186718 | AATAAAAGTCAAAAC[A/C]GTTGAAGAAAAAATA | 9474 |
rs778217252 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202703 | GTCTCGCTCTGCCAC[A/C]CCGGCTGGAGTGCAG | 9474 |
rs778267924 | snp | A/G | 8.27561e-05 | 0.00643205 | intron-variant | ATG5 | GRCh38.p7 | 6:106293003 | TATCACAAATGGGAC[A/G]AAGGAGAAATGCAAT | 9474 |
rs778273467 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231541 | AAAACTAGAAAGAAG[C/T]CTGTGAGTTATTCAA | 9474 |
rs778298209 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106244354 | TTAAGATCTCCCATT[A/C]TTTACAGGATACAGA | 9474 |
rs778330360 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273043 | TATACAATGTAATCT[C/T]AGTGTTCCAAAGACT | 9474 |
rs778353408 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230668 | TTTCAGATAGGAAAC[A/G]TTCCCCTCAAGGCAA | 9474 |
rs778355878 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292184 | AACATGGTGAAATCA[C/T]TGCTATTTGAGAATG | 9474 |
rs778368493 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251675 | GAAGGGAGGGGGAGG[C/G]GGAGAGAAAGAAAGA | 9474 |
rs778375458 | in-del | -/TTC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274402 | TGGTTTCATAAGCTT[-/TTC]TTATTTCTCTTTCAC | 9474 |
rs778415964 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319016 | AATGTAAAATGTGGA[-/T]GCCAGACTGTCTGGA | 9474 |
rs778445887 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208523 | GAATCATGAAATTCA[-/G]AAGTTTACGTTTTAA | 9474 |
rs778458301 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228767 | ATACTGGGCACCTGT[C/T]GGCCGGTTAAAAACG | 9474 |
rs778467103 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320142 | AAAATTAGAAGCCAC[A/T]TCCTAACTCAGGTTT | 9474 |
rs778470870 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301840 | TAACTCACTTAATTC[C/T]TGAAACAAAGTTACG | 9474 |
rs778502251 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318869 | GTGAATACACTTAAC[-/T]TTTAAAAATATGTAA | 9474 |
rs778549614 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259611 | TCCCTTCATCACCTT[-/G]TCTCTTCTGCTCCTT | 9474 |
rs778568747 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106210713 | TGACCCTAGTCAAAT[A/T]CTTAAACCTTCTTGT | 9474 |
rs778572434 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106320430 | TAAAGGTATTAAGTG[A/G]GCAGGTGCAATATAT | 9474 |
rs778590148 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296294 | TAAATCTAAGATATA[-/T]TTTTAGGGTCTTAAT | 9474 |
rs778602101 | in-del | -/TTATT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106290200 | TTGGCTTATTTTATT[-/TTATT]TTATTTTATTTTATT | 9474 |
rs778608675 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106223752 | CATACATGGTGAAAT[A/G]TTTAAAAATAGCTCA | 9474 |
rs778614569 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261272 | TAGTAGTCACCTCAG[-/A]AAAAGTAAATAATCA | 9474 |
rs778641237 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241008 | AAATACAAAAATTAG[C/T]CGGGCATGGTGGTGG | 9474 |
rs778662017 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212154 | TCTAGAAAAGGGATG[A/G]ACTCTGGAAATATCA | 9474 |
rs778666019 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106293057 | TGATGTTCCAAGGAA[A/G]AGCTGAACTTGATGC | 9474 |
rs778718615 | snp | C/T | | | | | GRCh38.p7 | 6:106185243 | TCACTTCAGCATTTG[C/T]ATAATTTTTTATAAG | 9474 |
rs778797659 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229500 | GAGAGAGACAAAGAG[A/G]AGAAAGAGGCAGAGA | 9474 |
rs778838999 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106292289 | TCGTAATCAATTAAT[A/G]TAAGTGTTTCCAATC | 9474 |
rs778864364 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106274363 | AAACACTGAAAGGCA[C/T]AGTATGTCCTAAATG | 9474 |
rs778907762 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250029 | CATATTTTCTCCCGT[G/T]CTGTACATTGTTTTT | 9474 |
rs778910936 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106205117 | AAGGCTTTTTCTGAC[A/G]ACTAATGGAAAGCAG | 9474 |
rs778942153 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188007 | AGGTATCACTTTATA[A/C]TACTACTAACCTAAA | 9474 |
rs778964923 | in-del | -/AAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265980 | AAGCTAGCACAAGAC[-/AAG]AATAATTAAGATCAG | 9474 |
rs778967257 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106264447 | GGAGAACTTCCCCCA[C/G]CAAGCAAGACAGGCC | 9474 |
rs779008078 | in-del | -/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230526 | GTGAGCATAACTAAT[-/C]CGATAAGCAGAGGTC | 9474 |
rs779008806 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257752 | TATTTCAAATCTACC[G/T]AATCTGTACATGGTA | 9474 |
rs779035963 | snp | A/G | 8.2426e-05 | 0.0064192 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316129 | GCTTCCCTTTCAGTT[A/G]TCTCATCCTGATATA | 9474 |
rs779052629 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309548 | TAAGTTATTCTTTTA[C/T]AAAGAAATAACTGTG | 9474 |
rs779071234 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216099 | ACTATAGAAAATAAG[C/T]GTTGGCAAGGATGTG | 9474 |
rs779072197 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106305977 | TACTTAAAAACACTA[A/C]AGGAAAAGATGCATC | 9474 |
rs779107462 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258891 | GTATTTAGAGATGAC[A/G]GAACAGCACAGCTAG | 9474 |
rs779110372 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196278 | TAAAATAAAGAGTAA[A/G]GAAAAAGCAAGTATT | 9474 |
rs779121140 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106276131 | AGGCCTCTACAGATA[C/T]CAATGAAGCAAACCT | 9474 |
rs779125126 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313640 | AACATAATGCTCAGT[A/G]ATAAACATATAGGAT | 9474 |
rs779191423 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252807 | TATTCACCTCCTGGT[A/C]TTTAACATCTAAGAA | 9474 |
rs779193373 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192661 | ATAACCATTGTGTTC[A/T]GCTTTGTAGCTTCAT | 9474 |
rs779233954 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193451 | TTTGCTTATAATCTC[-/TG]TATTTCTTAGTAAGG | 9474 |
rs779249120 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106226680 | GAGTATATTCTCTTT[A/T]TATCAGCTCTTTTTA | 9474 |
rs779280595 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202052 | TCTGCAGCCACAGGA[C/T]GAAACAGCTTCTGAA | 9474 |
rs779288978 | in-del | -/TTAA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192585 | CAAGAAAATTTCAGT[-/TTAA]TTAATTTTTTAAAAG | 9474 |
rs779360455 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106247358 | AAATGTCAATATTTA[C/T]GCCAGCACTTTTAAA | 9474 |
rs779367439 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106197457 | TGGTTGCTTGTCCCC[A/G]CCAAACCTCGTGTTG | 9474 |
rs779415622 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280477 | TTACTATAAGTCAAT[C/T]AGACCTCAATAAAGC | 9474 |
rs779432481 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106190932 | GAGAGGGCCAATTAT[G/T]CACCACTAGTTAGCA | 9474 |
rs779442790 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231911 | TGGAAAAGGGAAAAG[A/C]TAGGCAAATCAAATG | 9474 |
rs779459537 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310967 | AAGTATTCCATGACT[C/T]TGATACAAGTGATTC | 9474 |
rs779470778 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106265371 | GTTCTTCAAGATCTA[C/T]GAAGAGACTTGAACT | 9474 |
rs779507473 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227734 | GTAAGAAAATTAAGA[C/T]AGCCTTGTTTGATAA | 9474 |
rs779507869 | in-del | -/AGTTGAAG | 5.11426e-05 | 0.00505655 | intron-variant | ATG5 | GRCh38.p7 | 6:106186718 | AATAAAAGTCAAAAC[-/AGTTGAAG]AAAAAATAATCTGGT | 9474 |
rs779509453 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106279205 | TTTTCCTTGGGAGTA[C/T]TTTCTAAACCACAGC | 9474 |
rs779509872 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202905 | TGAGCTCAGGCAATC[C/T]GCCGGCTTCGGCCTC | 9474 |
rs779517296 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106278925 | ACTAAACTAGCAATA[A/G]AGTTTGCATTTTATG | 9474 |
rs779574931 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237325 | TTCATTAACTGAACC[A/T]AACTATGCCCATGAA | 9474 |
rs779584714 | in-del | -/CTAG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319411 | AATCGTTTGATATGC[-/CTAG]CTGTGTGGCAGGTGC | 9474 |
rs779591514 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106282591 | TGATCTTAGTTTGGT[-/A]AAAACATTCGATAAA | 9474 |
rs779600061 | snp | C/T | 3.29843e-05 | 0.00406092 | missense, synonymous-codon, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106202077 | TCTGAATGAAAGGTC[C/T]TTCAGTCGTTGTCTA | 9474 |
rs779623794 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273195 | ACTTTTACACCACCT[C/G]CAACTACAACAGAAC | 9474 |
rs779684278 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218991 | GGAGGAAAAGTGGGA[C/G]AAAAATGTAAAGAAA | 9474 |
rs779687893 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309771 | AAAAAAGCAAAACAG[C/T]GTCGCAAACTAGCTG | 9474 |
rs779698427 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229868 | AGCACACCTCACCGG[C/T]TCAGAATTATTCTAA | 9474 |
rs779700924 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106291019 | TTTCAAGAAAATGTC[C/T]AACAAATAACAAAGT | 9474 |
rs779717046 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200414 | TAATGCATTACCTGT[C/T]TCCTTCATGGATTTA | 9474 |
rs779729899 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106325177 | TTTGGACAGACTCAC[A/G]CTGCACTGTGCAATA | 9474 |
rs779730356 | in-del | -/ACAC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312632 | AAAGACTACACACAC[-/ACAC]ACACACACACACACA | 9474 |
rs779734883 | in-del | -/TGTA | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185871 | TAAAAAGTGATCTAC[-/TGTA]TGTATGTGAGTCAGA | 9474 |
rs779743818 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213559 | ATAGAGAAAGAGATA[A/C]AGTCATTTGAGTATT | 9474 |
rs779747057 | in-del | -/TTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106228491 | GGCTTCTAATAGAGC[-/TTT]TATAACACTCACCGC | 9474 |
rs779763336 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194835 | GACTGGGAAATGAAG[C/T]ATAATTGGGTAAAGC | 9474 |
rs779774085 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106229619 | GTAAAACCTATAATT[A/G]ATAATTGAAGGTCTT | 9474 |
rs779790807 | in-del | -/TCCT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262180 | AGGTTCAAGTGATTC[-/TCCT]TCCTGCCTCAGCCTC | 9474 |
rs779799313 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106241405 | TGGTGGGAATGTAAA[A/G]TGGTACAGCTACTAC | 9474 |
rs779814301 | snp | A/C/T | 3.56127e-05 | 0.00421963 | intron-variant | ATG5 | GRCh38.p7 | 6:106308330 | TAAAGCTAGTATATA[A/C/T]TTAATGCTTAATAAT | 9474 |
rs779814816 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242124 | TATATCTATCTATAT[C/G]TATACACACATACTC | 9474 |
rs779823298 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321134 | CCTGATTTCCACCTA[C/T]TAGTTACGTGTCTTG | 9474 |
rs779828567 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106317092 | GGTATGGCATAAGGA[C/G]ATGGCTTTTGACCTC | 9474 |
rs779836336 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106219960 | TACCAACCTGCTTAT[A/C]CCCTCCAAGCAATAT | 9474 |
rs779858397 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106297718 | TGCAAAATGACTTAA[-/AC]ACACACACACACACA | 9474 |
rs779913177 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301014 | GGTTTACTTACAAAG[C/T]ATTCTTCGGAAGGAC | 9474 |
rs779932878 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208047 | CAGTGAGCCGAAATC[A/G]CGCCACTGCACTCTA | 9474 |
rs779940011 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267961 | TAAAACACCAAAAGC[A/G]ATGGGAACAAAAACC | 9474 |
rs779956355 | in-del | -/AAAT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239542 | ATGAAAAAAGGAGAC[-/AAAT]GAATTGCTCCAACAG | 9474 |
rs779958269 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237077 | CCACTCCACATCCAC[C/T]GTACCTGAAATAGCC | 9474 |
rs780025620 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298137 | CCTGGCTAATGTTTG[-/T]TATTTTTAGTAGAGA | 9474 |
rs780037681 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285697 | TAGCCGCAAAGCAGT[C/T]ATAGACAATATGTAT | 9474 |
rs780072060 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106298255 | TGGGCCACTGCACCC[A/G]GCGCTAGCCTGTCAA | 9474 |
rs780075023 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202799 | CCCAAGTAGCTGGGA[A/C]TACAGGAGTGCGCCA | 9474 |
rs780083091 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106217324 | GATACTGAAAATGAA[G/T]CTGAAAAGTTTTGAA | 9474 |
rs780088721 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259121 | TGTTCAAGAAGTATT[C/T]TCCTCAAAACTGTTA | 9474 |
rs780097751 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295026 | CCAGGAAAAACTCTC[A/G]CCTCAGTCAAAACCT | 9474 |
rs780116045 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313452 | ACCATGGGTCCAATC[A/G]TGATTTCCTCTAGAA | 9474 |
rs780128916 | in-del | -/T | 1.66653e-05 | 0.00288658 | intron-variant | ATG5 | GRCh38.p7 | 6:106293123 | AAAAATGAAACAGTA[-/T]TATTTTGAGAAAATA | 9474 |
rs780165456 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106233244 | TTCTGGCTTATCCTC[A/G]TCCCAAAACCCTAAA | 9474 |
rs780174320 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235079 | ATTGAATACAACGTA[C/G]AACAGAGGAGCTTCA | 9474 |
rs780174821 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193450 | TTTTGCTTATAATCT[C/T]TGTATTTCTTAGTAA | 9474 |
rs780187657 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106308232 | TAGTAATAGTCTAAA[C/T]TTCACATATTGTATG | 9474 |
rs780218432 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212231 | TTCTAAGTAGCATTA[A/G]TTGAACTGAAAAGGC | 9474 |
rs780219305 | snp | C/T | 1.65696e-05 | 0.00287828 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186549 | GATCCTTCAATCTGT[C/T]GGCTGTGGGATGATA | 9474 |
rs780224951 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106280642 | ACTGAAAAAAAGATA[A/G]TAACAGCTAACAGTT | 9474 |
rs780232007 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106324992 | AAAATCTAGAACCAA[C/T]AGTTTCCTAGGTTCC | 9474 |
rs780241290 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248551 | ACACCAGGTAGAGGA[C/T]AGATGTCTTGACTCT | 9474 |
rs780283357 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106313657 | TAAACATATAGGATA[C/T]AGGCGGAAAGATTAT | 9474 |
rs780335043 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187181 | GTTTTCAGTAAAGCA[C/T]TCAAGTATGTATCAA | 9474 |
rs780377908 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194222 | GAGGTTTGGGAATTG[A/G]AGTTTTTTTTATTCC | 9474 |
rs780391572 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204023 | ACAACTGGGAGCTGA[A/T]CAACGAGAACACATG | 9474 |
rs780450111 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106213593 | AGGGCAGACTGAATA[C/T]AATGGTACTTCTGAG | 9474 |
rs780471238 | snp | G/T | 3.29625e-05 | 0.00405958 | missense, utr-variant-5-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106316149 | ATCCTGATATAGCGT[G/T]AAACAAGTTGGAATT | 9474 |
rs780502876 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106303780 | AAATGTCATCTATTA[C/T]AGCAACCAGCTAAGG | 9474 |
rs780511131 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106288935 | AACTACTGATCCAAA[-/TG]TGTGTGTGTGTGTGG | 9474 |
rs780569485 | in-del | -/TATC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106273343 | TTATTTCTGGAAAGT[-/TATC]TATTTCCTTCTACCT | 9474 |
rs780602125 | in-del | -/TTTTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194546 | TTCTTTTTCTTTTTC[-/TTTTT]TTTTTGAGATGGAGT | 9474 |
rs780607096 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189495 | GCGTGGTGGTGCATG[C/T]CTGTAGTTCCAGCTA | 9474 |
rs780613509 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106192778 | TAATACTGCCTAGAA[A/G]TTTTAAAAAATAGAG | 9474 |
rs780614593 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106254915 | TATGCAATTGAGCAG[A/C]CTTTGCTAGCCATAA | 9474 |
rs780669057 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300685 | ACTACACTGAATACT[C/T]TAGACAACTGTAACA | 9474 |
rs780714869 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106188554 | CAATATGGTAAACAA[G/T]CCACTGATGATGCAC | 9474 |
rs780718957 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106194675 | CCCAAGTAGCTGGGA[A/T]TACAGGCATGCACCA | 9474 |
rs780724837 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204216 | TGTATTCCAGAACTT[-/A]AAAGTATAATACAAA | 9474 |
rs780762212 | in-del | -/TATTA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106193359 | TACATTTTATATCTT[-/TATTA]TATTTTCAGAGCTTT | 9474 |
rs780762373 | snp | C/T | 1.65488e-05 | 0.00287647 | synonymous-codon, missense, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106248150 | AATGTTATTTCCTAC[C/T]TGATATATTCTAAAG | 9474 |
rs780763228 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106262138 | AGTGCAGTGGCACCA[C/T]CTCGACTCACTTCAA | 9474 |
rs780781770 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221027 | CTACCAAGAATGTAT[G/T]ATGCCAGCAGTAAAT | 9474 |
rs780821678 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106208269 | CTGTGTAAACACATA[G/T]GTATATGTATAAATG | 9474 |
rs780828486 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202620 | AAGAAATTCATTGTT[C/T]AAGTGTTTAGGAAAG | 9474 |
rs780840026 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277550 | CTGAGCATGGTAGCT[C/T]ATGCCTATAATCCCA | 9474 |
rs780852574 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106250867 | TCACCCTTCAATATA[C/T]GCATCGCTATATGGT | 9474 |
rs780876588 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106319148 | CATTAGATACAAGAA[C/T]TAAATGAATACATGT | 9474 |
rs780952546 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106311187 | ACTCCAATGTGTAAA[G/T]CATCATACTAGGCAA | 9474 |
rs780962025 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106230615 | GGACTAATGCTCATC[A/G]GAAAATGACTAGTGG | 9474 |
rs780978559 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106209407 | CTCAAGGGAGTTATG[C/T]TATGTGAAAAAAGTC | 9474 |
rs781002469 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106202693 | TGGAGACAGAGTCTC[A/G]CTCTGCCACCCCGGC | 9474 |
rs781011145 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231663 | TCAACTGACTCTACT[A/G]AAGGCCAACTAATCT | 9474 |
rs781016114 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318445 | CAAAAGAGATACAAA[C/T]ATAGACTTAGAAGGC | 9474 |
rs781019521 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106214048 | AAAGAAAAAGAAAAC[A/G]GGGGTTTACACAGGA | 9474 |
rs781032088 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322977 | CAGGCTGGAGTGCAG[A/T]GGCGCAATCTCGGCT | 9474 |
rs781044335 | in-del | -/T | | | downstream-variant-500B | ATG5 | GRCh38.p7 | 6:106184098 | GTCAGTGGATTTTTT[-/T]ATCCTTACATAACTC | 9474 |
rs781071578 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106252574 | CTGCAGGAAAAAGTG[A/G]TAACTTTAAAGGATT | 9474 |
rs781079568 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106258008 | ACAAGTACACAAGAG[A/T]TTGTTCCTTTCACTT | 9474 |
rs781108210 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227780 | TAACTGTTCTTGCAC[A/T]GTTCTGGTTATTGTC | 9474 |
rs781117229 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106287118 | ATTTATAGCTGGGAA[A/G]TGCAGGCAGTGATAG | 9474 |
rs781119388 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106270515 | CTCCATATTTCATTG[C/T]TTTGTATGACTGTGA | 9474 |
rs781146358 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106309116 | AAGAAGGAGCTTGGC[A/G]AAAATTTATGGTTTT | 9474 |
rs781185275 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106300364 | TATGATTAAAATGTT[-/A]AAATGTTTTTTAAAA | 9474 |
rs781205813 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106285852 | GTAAAAACTACTCTT[A/T]TATCACAGGCCATGC | 9474 |
rs781206689 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106239329 | AAATCTATGCAGAAC[A/G]TAAAACAAAATCTGA | 9474 |
rs781212296 | in-del | -/TCTT | | | intron-variant | ATG5 | GRCh38.p7 | 6:106204699 | CTGCACTCTCATCTC[-/TCTT]TCCTGCTGGCTTGTG | 9474 |
rs781234480 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206229 | CCCCAGGGAGCTTGT[A/G]AGGCTTTTGCCCCTT | 9474 |
rs781241628 | snp | C/T | 1.70374e-05 | 0.00291863 | synonymous-codon, intron-variant, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106308372 | CACTCACCATTTCAG[C/T]GGTGTGCCTTCATAT | 9474 |
rs781254990 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106218474 | CAATTGTATGTGATA[C/T]GGCTTAGAAAGGCAT | 9474 |
rs781287237 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106234180 | CCTCCCAACTGACCC[C/G]GGTACATAGCACCCC | 9474 |
rs781299448 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243774 | AGGCGGAGGTTTCAG[C/T]GAGCCGAGATTGCAC | 9474 |
rs781302799 | in-del | -/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106289530 | ATTTCCTTATTAACT[-/G]GTAAGATTCTTTTTT | 9474 |
rs781306268 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106221628 | GAGATCAAAGCTGCA[A/G]TGAGCTGAGATCGTG | 9474 |
rs781324564 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106296498 | GTGTTGCCTAAAGTA[C/T]TGAAACATCTTTCAA | 9474 |
rs781367752 | in-del | -/GGTAAG/GGTAAGTA | 5.54968e-05 | 0.00526743 | intron-variant | ATG5 | GRCh38.p7 | 6:106279874 | CACACATTACAAAAT[-/GGTAAG/GGTAAGTA]TAACCTCTTAAAAGA | 9474 |
rs781369357 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106266587 | CCCTGATGAACATCA[A/T]TGTGAAAATCCTCAA | 9474 |
rs781395189 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106314747 | AAATGGTATCCTAAC[A/C]TATATTACAGAACAA | 9474 |
rs781395931 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106235219 | TAACCTCCTTGTTAA[A/G]TTTGTCTCTTCCAGA | 9474 |
rs781418227 | in-del | -/AA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295278 | TGAATGTAGGCACTT[-/AA]TTAAAGTTTTATTCA | 9474 |
rs781484324 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106256883 | GTTACATTGAATTTA[C/T]TTAAAAATTAACTTA | 9474 |
rs781528027 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106248678 | CAGTGGCCCACGCCT[A/G]TAATCACAGCACTTT | 9474 |
rs781573261 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106249977 | GTTATAAGAGTTCTT[C/T]ATAAATTCTGAATAC | 9474 |
rs781601442 | snp | C/T | 3.31307e-05 | 0.00406992 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106186585 | ATGAAGAAAATTATC[C/T]GGGTAGCTCAGATGT | 9474 |
rs781648234 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106212310 | CTAACTATGAGTGTG[C/T]TTGTTCATGCCCAAA | 9474 |
rs781690646 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106255530 | AATAAACCATGACTG[C/T]AAGTTACAACATCTT | 9474 |
rs781696388 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295517 | AATTTGTAAGCAAAT[C/T]CTAAAACAAATATAT | 9474 |
rs781707323 | snp | C/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106224959 | TTCACCAGATATGTT[C/G]CACTGGTCATAAAAC | 9474 |
rs781730257 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106243810 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTTC | 9474 |
rs781735116 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106186948 | GCTTACTTAAGATTG[A/G]CGTTAATGAAACTGT | 9474 |
rs781766732 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242336 | AATGAGGACATCATG[A/G]TATGCGAAATAAGCC | 9474 |
rs796068355 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106301147 | TAGAGCACCCTCTGC[C/T]GACTAACATCTCAGT | 9474 |
rs796069323 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302489 | ATAAACTAAAAGTAA[C/T]AGTATTAAAAGCAGG | 9474 |
rs796084658 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106237038 | GTTTGAAGAATTCTC[A/C]AATTATTAACATATC | 9474 |
rs796093200 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106271404 | CCTTAGAAAACAGAC[C/T]CCAGAGAAAGCTCTG | 9474 |
rs796138787 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106199415 | CACTTGCTTCAATAC[A/G]GATGCAACTCAAATA | 9474 |
rs796221078 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106227567 | TGCCACTGCACTCTT[A/G]CAGTGGAGACCCTGT | 9474 |
rs796254148 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106261030 | ATTGTTGAGTTAAAA[A/T]GTGTATCTAGCCATC | 9474 |
rs796292816 | in-del | CACACACAC/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106312635 | ACTACACACACACAC[CACACACAC/T]CACACACACACACAC | 9474 |
rs796397608 | in-del | -/CA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106242155 | ACACACACACACACA[-/CA]TTTATAGAAGACAGG | 9474 |
rs796398886 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106189824 | CTCAGGAGAAAAATG[C/T]TACTGTATGCCTCTC | 9474 |
rs796411946 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106203076 | AAAAATATTAACTAA[C/T]GGTGATTCTAGGTAG | 9474 |
rs796517686 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286170 | TTTGGCTCCTCCTTC[C/T]CTGATACCCTGCCTA | 9474 |
rs796544070 | multinucleotide-polymorphism | GT/TA | | | intron-variant | ATG5 | GRCh38.p7 | 6:106267130 | CCTTAAGCTGTTAAT[GT/TA]ACTTCAGCAAAGTCT | 9474 |
rs796544894 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106295849 | GATTATAGGCATGAG[C/T]CACTATGTCCAGCCC | 9474 |
rs796553429 | in-del | -/AC | | | intron-variant | ATG5 | GRCh38.p7 | 6:106200884 | GCAGCAGGACATTTT[-/AC]ACACACACACACACA | 9474 |
rs796574553 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106277885 | AAATCCTAATATTTA[-/T]TTTAGTACTTATAAT | 9474 |
rs796648854 | snp | G/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106310810 | ATAATATTTGTCCTT[G/T]AGTGCCTGGTTTATT | 9474 |
rs796684264 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106206665 | AAAAAAAAAAAAAAA[-/A]GTACACACTCTAACA | 9474 |
rs796694413 | snp | A/G | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327184 | TCCCAGTGTCAGACA[A/G]AAGTATATAAAATTT | 9474 |
rs796699572 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106294845 | GAGACCTTTTCTCAA[A/G]AAAAAAAAAAAAAAA | 9474 |
rs796744301 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106318864 | TCTCCAGTGAATACA[A/C]TTAACTTTAAAAATA | 9474 |
rs796753707 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106286313 | TCCAAAGCACATGGG[A/G]CTCACCTTGTTTGTT | 9474 |
rs796765366 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187188 | GTAAAGCATTCAAGT[A/G]TGTATCAAAATGTCT | 9474 |
rs796789592 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106216973 | TATTAAAAAAAAAAA[-/A]GTTATCATATGGGTG | 9474 |
rs796799428 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106302696 | TTACAGTGAGCTCTT[A/T]TTTTACTACAATAGA | 9474 |
rs796813251 | snp | A/C | | | intron-variant | ATG5 | GRCh38.p7 | 6:106284319 | GAAGGGTCTAATTAA[A/C]CTATACCCTCTCCAT | 9474 |
rs796817737 | in-del | -/A | | | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327710 | CAAAAAAAAAAAAAA[-/A]TTGTTTTGGGGGAAA | 9474 |
rs796852465 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106259729 | AAAAATAATGACTTT[C/T]AAATACATGAAAAGT | 9474 |
rs796900087 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106187406 | TTGTGTTTTTCATGA[-/T]TTTGGTGTGTTGTAC | 9474 |
rs796900553 | in-del | -/A | | | intron-variant | ATG5 | GRCh38.p7 | 6:106196736 | TCAAAAAAAAAAAAA[-/A]GTAGATTGAAAGTTC | 9474 |
rs796916306 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106257353 | TTACTGTACATAATT[A/G]TATGTGCTAGACATT | 9474 |
rs796958952 | in-del | -/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106201176 | TTTCTTTCCCAAATG[-/T]TTTTTTATCTGCTGT | 9474 |
rs796966598 | in-del | -/TG | | | intron-variant | ATG5 | GRCh38.p7 | 6:106211299 | CACAATGCACTGGGT[-/TG]TAAAACTTAAAATGG | 9474 |
rs797003412 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106269483 | CAGGGAGGCTTGGCC[A/G]CACAGGAGCCCATGG | 9474 |