SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14503 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185978 | ATGCAATCTTGTAAC[A/T]TTGATAATGAACAGT | 9474 |
rs473543 | snp | C/T | 0.477345 | 0.103991 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106327811 | GAGAAAGAAAGAAAA[C/T]GGTCAATTTATAAAA | 9474 |
rs478310 | snp | C/T | 0.170084 | 0.236883 | intron-variant | ATG5 | GRCh38.p7 | 6:106217877 | ATCCCAACAGTATTT[C/T]AGATTGAGATAATAA | 9474 |
rs484621 | snp | C/T | 0.475259 | 0.108435 | intron-variant | ATG5 | GRCh38.p7 | 6:106286533 | ATGACCCTCCATGAT[C/T]TCCACCACCTGGTAT | 9474 |
rs490010 | snp | C/T | 0.466721 | 0.124627 | intron-variant | ATG5 | GRCh38.p7 | 6:106292583 | AATCTTGCATGTAGA[C/T]GTGGATATGGAAGTA | 9474 |
rs501804 | snp | A/G | 0.170733 | 0.237101 | intron-variant | ATG5 | GRCh38.p7 | 6:106299256 | ATAAGTAATCTAGCA[A/G]TAATTTAAAGTATAC | 9474 |
rs506027 | snp | C/T | 0.477175 | 0.104362 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326589 | GTTTACCAATTATTA[C/T]TATTTTTTTTTTGAG | 9474 |
rs510432 | snp | A/G | 0.47709 | 0.104548 | upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106326155 | AGAAGAAGATCAAAT[A/G]AGAAAATGGATGGGA | 9474 |
rs511472 | snp | A/G | 0.17138 | 0.237316 | intron-variant | ATG5 | GRCh38.p7 | 6:106223164 | TAGAACTTTTTTAGG[A/G]AATGCTTTATTTGTT | 9474 |
rs520296 | snp | A/G | 0.157972 | 0.232445 | intron-variant | ATG5 | GRCh38.p7 | 6:106291541 | CATTCAACAAATATG[A/G]AGATCCTTCTGTGTG | 9474 |
rs524428 | snp | A/G | 0.461703 | 0.132974 | intron-variant | ATG5 | GRCh38.p7 | 6:106281713 | acatacacttactct[A/G]tgacccagcatttct | 9474 |
rs532906 | snp | C/T | 0.466721 | 0.124627 | intron-variant | ATG5 | GRCh38.p7 | 6:106219394 | ATTAACTCAGCCACA[C/T]ATCTAACACAGTCAG | 9474 |
rs538557 | snp | C/T | 0.172351 | 0.237636 | intron-variant | ATG5 | GRCh38.p7 | 6:106236001 | atctctactacaccc[C/T]cctgacctggcccag | 9474 |
rs543465 | snp | C/T | 0.230017 | 0.2492 | intron-variant | ATG5 | GRCh38.p7 | 6:106300729 | GTATGCATCTAAACA[C/T]AGAAAGGATACTATA | 9474 |
rs546456 | snp | A/C | 0.454423 | 0.143914 | intron-variant | ATG5 | GRCh38.p7 | 6:106232263 | cttggatagtgacag[A/C]tctggaggaccgttg | 9474 |
rs547738 | snp | C/T | 0.467337 | 0.123551 | intron-variant | ATG5 | GRCh38.p7 | 6:106290848 | attttctgatgagat[C/T]ggtggttattttaac | 9474 |
rs549223 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106231968 | tggacaatctttttt[A/T]aagtgtccttgtaga | 9474 |
rs552852 | snp | G/T | 0.00472811 | 0.0483911 | intron-variant | ATG5 | GRCh38.p7 | 6:106248982 | CTTTGGTATTTAATG[G/T]TTACTGTGTTCAGTA | 9474 |
rs566140 | snp | A/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106278006 | gtggagtgtggtggc[A/T]caatcatggctcact | 9474 |
rs573775 | snp | C/T | 0.466824 | 0.124448 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106316991 | GCATTTACTGTTTCA[C/T]TGGGGCCAGAGGGCT | 9474 |
rs579801 | snp | A/G | 0.453087 | 0.145793 | intron-variant | ATG5 | GRCh38.p7 | 6:106228260 | tttcactctccatcc[A/G]ccactgctgtttgcc | 9474 |
rs580187 | snp | A/T | 0.372189 | 0.218105 | intron-variant | ATG5 | GRCh38.p7 | 6:106319701 | TAAATACTATTGATA[A/T]AAACTTACAAGGGTA | 9474 |
rs585595 | snp | C/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106321427 | gcagtggcgccatct[C/T]ggctcactgcaagct | 9474 |
rs594819 | snp | G/T | 0.461259 | 0.133677 | intron-variant | ATG5 | GRCh38.p7 | 6:106228727 | ttgcttgctactctg[G/T]cctatcccttagaat | 9474 |
rs597443 | snp | A/G | 0.453818 | 0.144769 | intron-variant | ATG5 | GRCh38.p7 | 6:106321767 | gataaacagataact[A/G]cattgcatgatagtg | 9474 |
rs600076 | snp | A/G | 0.14933 | 0.228835 | intron-variant | ATG5 | GRCh38.p7 | 6:106217827 | TACAATATCTGAAGA[A/G]AGAATGGTCTATTGA | 9474 |
rs605457 | snp | G/T | 0.184203 | 0.241186 | intron-variant | ATG5 | GRCh38.p7 | 6:106254370 | AAATGTAAGTCCCAT[G/T]AGGGCAAAGACTTTA | 9474 |
rs606093 | snp | A/T | | | intron-variant | ATG5 | GRCh38.p7 | 6:106322848 | aatttctaaatggaa[A/T]tgtcatatgtggggg | 9474 |
rs617994 | snp | G/T | 0.47741 | 0.118366 | intron-variant | ATG5 | GRCh38.p7 | 6:106219536 | GTATAACAACTATTT[G/T]CACAGTGTGTACATG | 9474 |
rs626664 | snp | A/G | 0.224709 | 0.248717 | intron-variant | ATG5 | GRCh38.p7 | 6:106306835 | TCAGGAGAATTGGAG[A/G]TTTTGGAATGGGAAG | 9474 |
rs627484 | snp | C/T | 0.149999 | 0.229128 | intron-variant | ATG5 | GRCh38.p7 | 6:106262808 | aggtactgtgctacc[C/T]ggctgggttactaca | 9474 |
rs632686 | snp | A/C | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106269193 | atgcaccaatcgaca[A/C]tctgtaactagctac | 9474 |
rs633724 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | ATG5 | GRCh38.p7 | 6:106286165 | TACACTTTGGCTCCT[C/T]CTTCTCTGATACCCT | 9474 |
rs638659 | snp | A/G | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106277963 | AATTAttttttttta[A/G]agacagggtctcact | 9474 |
rs641713 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ATG5 | GRCh38.p7 | 6:106233118 | gccacaggtagcgag[A/G]aaatttaagagcact | 9474 |
rs644232 | snp | G/T | 0.471768 | 0.115407 | intron-variant | ATG5 | GRCh38.p7 | 6:106309539 | TTCTTTATAAAAGAA[G/T]AACTTATATTCTGTT | 9474 |
rs646351 | snp | A/G | 0.498415 | 0.0281103 | intron-variant | ATG5 | GRCh38.p7 | 6:106249797 | atgcctgccagaatg[A/G]ttataattaaaaaga | 9474 |
rs646438 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG5 | GRCh38.p7 | 6:106249735 | actaattggaatcca[A/G]atacattgctggtgg | 9474 |
rs651574 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ATG5 | GRCh38.p7 | 6:106227891 | TCTCCTTCAAGTTGA[A/G]TTACAACTAGTAATT | 9474 |
rs652421 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ATG5 | GRCh38.p7 | 6:106292272 | TTAATTGATTACGAA[C/T]AGTAATTCATTCTCA | 9474 |
rs656994 | snp | C/T | 0.184521 | 0.241273 | intron-variant | ATG5 | GRCh38.p7 | 6:106252729 | GATTGCTACTCAGGC[C/T]CAATTCAGCTGGCTA | 9474 |
rs660350 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106248963 | CTGTGTTCAGTATTT[C/T]GACTCTATTTTTATA | 9474 |
rs662114 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | ATG5 | GRCh38.p7 | 6:106319061 | TGACTTACTTGAGGT[C/T]ACACTGTAAGTGGTG | 9474 |
rs665791 | snp | C/T | 0.472335 | 0.114312 | intron-variant | ATG5 | GRCh38.p7 | 6:106226975 | tgtatattggtatgc[C/T]tgatggtgtctcttg | 9474 |
rs669975 | snp | C/T | 0.471673 | 0.115589 | intron-variant | ATG5 | GRCh38.p7 | 6:106305373 | AAAATATGACTTTAT[C/T]TTCCTGTTGGTAGGA | 9474 |
rs671116 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | ATG5 | GRCh38.p7 | 6:106312722 | TCCCATCTTGTGGCA[C/T]TGTCCTGTTAGCCCT | 9474 |
rs672070 | snp | C/G | 0.185155 | 0.241444 | intron-variant | ATG5 | GRCh38.p7 | 6:106230937 | aaatcacacttttta[C/G]ataattgcgagttgt | 9474 |
rs676090 | snp | C/T | 0.170408 | 0.236992 | intron-variant | ATG5 | GRCh38.p7 | 6:106301192 | AATGGAAAGTGCTGG[C/T]CTAACTCAAAATAGA | 9474 |
rs676099 | snp | A/G | 0.162581 | 0.234218 | intron-variant | ATG5 | GRCh38.p7 | 6:106301203 | ATTACATGGGAAATG[A/G]AAAGTGCTGGCCTAA | 9474 |
rs676371 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ATG5 | GRCh38.p7 | 6:106247710 | ATTTTTGTGCTTTTT[A/G]TTAGTGATTTTGCTG | 9474 |
rs676640 | snp | A/G | 0.159292 | 0.232964 | intron-variant | ATG5 | GRCh38.p7 | 6:106259007 | TGAGTAATATTTTCA[A/G]TTGATTATCACAATG | 9474 |
rs679160 | snp | A/C | 0.497359 | 0.0362457 | intron-variant | ATG5 | GRCh38.p7 | 6:106267130 | actttgctgaagttt[A/C]ttaacagcttaagga | 9474 |
rs698029 | snp | A/G | 0.471292 | 0.116318 | intron-variant | ATG5 | GRCh38.p7 | 6:106195365 | TTCAACTTAAGTTGA[A/G]TGCAGGTGTGTCAAA | 9474 |
rs698031 | snp | C/T | 0 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106227495 | cagctactcaggcgg[C/T]taaggtggaaagatc | 9474 |
rs710088 | snp | C/T | 0.172028 | 0.23753 | intron-variant | ATG5 | GRCh38.p7 | 6:106187568 | TCTGGGTTTGTCTCC[C/T]TTACCTTCTCTTCAA | 9474 |
rs710089 | snp | C/T | 0.17138 | 0.237316 | intron-variant | ATG5 | GRCh38.p7 | 6:106191750 | GTGTCAAAAATGTAA[C/T]TGATAAAGTATGTGA | 9474 |
rs710090 | snp | A/C | 0.168135 | 0.236216 | intron-variant | ATG5 | GRCh38.p7 | 6:106197078 | GCTGCTGTTAGGGGA[A/C]AGATCATTACAGAAC | 9474 |
rs710091 | snp | C/T | 0.17461 | 0.238362 | intron-variant | ATG5 | GRCh38.p7 | 6:106284658 | ccacacccagccttg[C/T]acatcatctttttga | 9474 |
rs796707 | snp | A/G | 0.214843 | 0.247516 | intron-variant | ATG5 | GRCh38.p7 | 6:106245646 | TCTCTCTCCGGTTAT[A/G]CAGAAATTCTATTAG | 9474 |
rs803360 | snp | C/G | 0.471958 | 0.115042 | intron-variant, upstream-variant-2KB | ATG5 | GRCh38.p7 | 6:106318254 | TTAATAGGCAGGGAT[C/G]ATCATAAACCAAAAC | 9474 |
rs960323 | snp | A/G | 0.21695 | 0.247806 | intron-variant | ATG5 | GRCh38.p7 | 6:106209954 | gcagcctgagaatct[A/G]cattttaataagatc | 9474 |
rs1044481 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ATG5 | GRCh38.p7 | 6:106185145 | TTCTTCACAAAATTA[G/T]ATAAAGTTGGTCAAA | 9474 |
rs1066914 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ATG5 | GRCh38.p7 | 6:106233687 | gtagacatctcataa[C/T]gtgaacggcatactc | 9474 |
rs1181379 | snp | A/G | | | intron-variant | ATG5 | GRCh38.p7 | 6:106251661 | agggagggagggagg[A/G]agggagggaggCGga | 9474 |
rs1475270 | snp | A/G | 0.453697 | 0.14494 | intron-variant | ATG5 | GRCh38.p7 | 6:106239504 | TCATGGAAAATTAAT[A/G]ACTGAGAATAACCAT | 9474 |
rs1623780 | snp | A/G | 0.163236 | 0.234461 | intron-variant | ATG5 | GRCh38.p7 | 6:106274741 | TGTTAGTATTAGAAA[A/G]GAATAAAATAAAGAA | 9474 |
rs1624009 | snp | A/T | 0.224709 | 0.248717 | intron-variant | ATG5 | GRCh38.p7 | 6:106292397 | GCACTTCATAAAATA[A/T]TGAGACAAAATTAGG | 9474 |
rs1624701 | snp | A/G | 0.166699 | 0.235714 | intron-variant | ATG5 | GRCh38.p7 | 6:106279844 | TATCCTGTTTTATAT[A/G]TATATTTTTTCCTTT | 9474 |
rs1626224 | snp | C/T | 0.162253 | 0.234095 | intron-variant | ATG5 | GRCh38.p7 | 6:106220964 | TATCCAATAGTAAAG[C/T]TGAAGAAATAAACAT | 9474 |
rs1626503 | snp | A/G | 0.164219 | 0.234823 | intron-variant | ATG5 | GRCh38.p7 | 6:106262217 | ttaggcatggcacac[A/G]cctctaatccgagct | 9474 |
rs1627312 | snp | A/G | 0.158962 | 0.232835 | intron-variant | ATG5 | GRCh38.p7 | 6:106262158 | TTGAACCTGGGAGGC[A/G]GAGGTTGAAGTGAGT | 9474 |
rs1766191 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ATG5 | GRCh38.p7 | 6:106301683 | gaaatgcttcaataa[C/G]cagcagttcctttga | 9474 |
rs1766192 | snp | A/G | 0.164219 | 0.234823 | intron-variant | ATG5 | GRCh38.p7 | 6:106299631 | ACAAAAAGCAAAGAA[A/G]TATTAAAATATATTC | 9474 |
rs1766193 | snp | G/T | 0.35574 | 0.226537 | intron-variant | ATG5 | GRCh38.p7 | 6:106230628 | tcggaaaatgactag[G/T]ggtgctggcatccct | 9474 |
rs1766194 | snp | C/T | 0.355311 | 0.226737 | intron-variant | ATG5 | GRCh38.p7 | 6:106230896 | gtgtgaagtgtcata[C/T]gtacaaactttcttt | 9474 |
rs1766196 | snp | G/T | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106231545 | CTAGAAAGAAGCCTG[G/T]GAGTTATTCAATGAT | 9474 |
rs1766199 | snp | A/G | 0.224709 | 0.248717 | intron-variant | ATG5 | GRCh38.p7 | 6:106307347 | AACTGTATCCAAATG[A/G]TAGCATTTCAACATT | 9474 |
rs1766200 | snp | C/T | 0.225597 | 0.248806 | intron-variant | ATG5 | GRCh38.p7 | 6:106293588 | TACATTTCCAGTCTT[C/T]TACCTACACATACAT | 9474 |
rs1766202 | snp | A/T | 0.224412 | 0.248687 | intron-variant | ATG5 | GRCh38.p7 | 6:106267131 | GACTTTGCTGAAGTT[A/T]ATTAACAGCTTAAGG | 9474 |
rs1766205 | snp | A/G | 0.165853 | 0.235413 | intron-variant | ATG5 | GRCh38.p7 | 6:106259905 | AGTATTCCATGGTTT[A/G]TATGTGCCACATTGT | 9474 |
rs1766207 | snp | A/T | 0.5 | 0 | intron-variant | ATG5 | GRCh38.p7 | 6:106246394 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 9474 |
rs1766208 | snp | A/G | 0.37138 | 0.218556 | intron-variant | ATG5 | GRCh38.p7 | 6:106305574 | AATTAGTCGCCAGTT[A/G]AGACAACTCATAAGT | 9474 |
rs1769962 | snp | A/G | 0.165527 | 0.235296 | intron-variant | ATG5 | GRCh38.p7 | 6:106293819 | ATTGAAATCTACAAC[A/G]TTTGTATTAGTCATG | 9474 |
rs1769963 | snp | C/T | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106220116 | CAAAGTCAGATGATA[C/T]AACTGAATGTTTATG | 9474 |
rs1769964 | snp | A/G | 0.164219 | 0.234823 | intron-variant | ATG5 | GRCh38.p7 | 6:106221559 | CGCCTGGTGGTGTGC[A/G]CCTGTAGTCCCAGCT | 9474 |
rs1769965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATG5 | GRCh38.p7 | 6:106304820 | acaggcgtgagccac[C/T]gtgcctggccAATTC | 9474 |
rs1769968 | snp | G/T | 0.209084 | 0.246629 | intron-variant | ATG5 | GRCh38.p7 | 6:106231651 | CTTCAGTAGAGTCAG[G/T]TGACAGAGAGAGGTA | 9474 |
rs1769969 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ATG5 | GRCh38.p7 | 6:106231157 | gagagaaaaaggtac[A/G]tgcactctggctggg | 9474 |
rs1769970 | snp | A/C | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106228323 | GGAGCACAACGGACA[A/C]CCTGCTAGATCCAGA | 9474 |
rs1769971 | snp | C/T | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106228120 | AATAAAGCTATTTTC[C/T]AATAACCAAATAGTT | 9474 |
rs1769972 | snp | A/G | 0.164873 | 0.23506 | intron-variant | ATG5 | GRCh38.p7 | 6:106227944 | TTAAGCTTTTTTACA[A/G]TTCATTGCTGCCTGG | 9474 |
rs1769974 | snp | C/T | 0.164219 | 0.234823 | intron-variant | ATG5 | GRCh38.p7 | 6:106249458 | CGGCTGAATAATATT[C/T]CATTATGTGGAGTTA | 9474 |
rs1769975 | snp | A/G | 0.1652 | 0.235179 | intron-variant | ATG5 | GRCh38.p7 | 6:106278297 | GTTTGAAGAGTGCTT[A/G]CTTTCTCAACATATA | 9474 |
rs1769976 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ATG5 | GRCh38.p7 | 6:106278952 | tatgtcattatctgc[A/G]gttaatataccacag | 9474 |
rs1769978 | snp | A/C | 0.21695 | 0.247806 | intron-variant | ATG5 | GRCh38.p7 | 6:106319038 | CTGTCTGGAGCCAAA[A/C]CCAGCTCCACCACTT | 9474 |
rs1769979 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ATG5 | GRCh38.p7 | 6:106319080 | tcaagtaagtcattt[A/C]acttctctatttctg | 9474 |
rs1769980 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ATG5 | GRCh38.p7 | 6:106299680 | TTTATGTGTGTGTGT[A/G]TGTTTGTGCATGTGT | 9474 |
rs1769981 | snp | G/T | 0.167809 | 0.236103 | intron-variant | ATG5 | GRCh38.p7 | 6:106254359 | TCCCTCAACCAAAAT[G/T]TAAGTCCCATGAGGG | 9474 |
rs1832408 | snp | C/T | 0.219049 | 0.248077 | intron-variant | ATG5 | GRCh38.p7 | 6:106234165 | atgtaaaggaagtaa[C/T]ctcccaactgacccg | 9474 |
rs1885450 | snp | C/T | 0.365646 | 0.221644 | intron-variant | ATG5 | GRCh38.p7 | 6:106195186 | AAATACTAGTACATT[C/T]GACTTTCATATGATG | 9474 |