SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4797 | snp | A/G | 0.475157 | 0.108647 | synonymous-codon | SQSTM1 | GRCh38.p7 | 5:179833213 | GGCGGAGCAGATGAG[A/G]AAGATCGCCTTGGAG | 8878 |
rs4935 | snp | C/T | 0.468854 | 0.120843 | synonymous-codon | SQSTM1 | GRCh38.p7 | 5:179833153 | CAGCTGCTGCTCTGA[C/T]CCCAGCAAGCCGGGT | 8878 |
rs10173 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837226 | AATTTGTAAACAATC[C/T]AATTAAATGGCATGC | 8878 |
rs10277 | snp | C/T | 0.468127 | 0.12215 | missense, utr-variant-3-prime, downstream-variant-500B | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837731 | GGTGGCAGGACAAAT[C/T]GCGCCCATTTAGAGG | 8878 |
rs14799 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837153 | CACCACTGTAGTTCT[C/T]TCATTTCCAAACCAT | 8878 |
rs14800 | snp | C/T | | | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837134 | AGCTGCCTCCTGGTC[C/T]CTTCACCACTGTAGT | 8878 |
rs14801 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837245 | TAAATGGCATCAGCA[C/T]TTTAANCNNNNNNNN | 8878 |
rs155787 | snp | A/G | 0.458315 | 0.13822 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833494 | TGCACGTGTGCATGC[A/G]TGCTCCCCGACTGTC | 8878 |
rs155788 | snp | C/T | 0.310878 | 0.242475 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833528 | CAGGAGCCAGGGCCA[C/T]GGTCAGGCTTGGCCT | 8878 |
rs155789 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834682 | tgtccactcagggtt[A/C/G]aatggattaagggcg | 8878 |
rs155790 | snp | C/T | 0.0105182 | 0.0717529 | utr-variant-3-prime | SQSTM1 | GRCh38.p7 | 5:179836676 | GCAGAGAAACTGGCC[C/T]GTACAGAGACCTGCA | 8878 |
rs166033 | snp | A/G | 0.412416 | 0.190055 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835335 | gaggctaaggcaggc[A/G]gctgggaggtggagg | 8878 |
rs169249 | snp | A/C | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179817790 | cgaggtggggggatc[A/C]cctgaagtcaggagt | 8878 |
rs172057 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | SQSTM1 | GRCh38.p7 | 5:179818959 | GGGGAGAGTGTCTGT[C/T]TGGCTCCAGCCGCTG | 8878 |
rs172058 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179818330 | ACTCATCCCCTGTGT[C/T]CCCTGTGATTGTCAA | 8878 |
rs173561 | snp | C/T | 0.452227 | 0.146984 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835108 | acggccaggcagagg[C/T]gctcctcacatccca | 8878 |
rs183889 | snp | A/C | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179817975 | agctgagatcgtgcc[A/C]ctgcacttcagcctg | 8878 |
rs185653 | snp | A/C | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179817882 | ggcttggtggcaggc[A/C]cctgtagtcccagct | 8878 |
rs248237 | snp | A/G | 0.4021 | 0.198407 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834001 | AAATGTTTTTCTTTA[A/G]GCAAACTCCAGAGCC | 8878 |
rs248238 | snp | A/G | 0.277778 | 0.248452 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834411 | GTAGTTCTTATTttt[A/G]tttatttatttattt | 8878 |
rs248239 | snp | A/T | 0.0916144 | 0.193427 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834517 | gagacccttgttcac[A/T]tgtttatctgctgac | 8878 |
rs248240 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834526 | ggaaaaccagagacc[C/T]ttgttcacatgttta | 8878 |
rs248241 | snp | C/T | 0.399968 | 0.200024 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835233 | aggggctcctcacat[C/T]ccagacgatgggcgg | 8878 |
rs248242 | snp | A/G | 0.449599 | 0.150533 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835733 | gcatcatcatagctt[A/G]gcatctactcataag | 8878 |
rs248244 | snp | C/T | 0.089084 | 0.191327 | intron-variant, downstream-variant-500B | C5orf45, SQSTM1 | GRCh38.p7 | 5:179838216 | AGGGCCTCGAGACAT[C/T]GGGAAAGGGGTGCGC | 8878 |
rs248245 | snp | A/G | 0.488057 | 0.0763479 | intron-variant, downstream-variant-500B | C5orf45, SQSTM1 | GRCh38.p7 | 5:179838261 | TACCTCCCACCGGGG[A/G]GCAGCTCTCCAGAGC | 8878 |
rs269445 | snp | C/T | 0.447162 | 0.153712 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179832030 | tttgggaggccgagg[C/T]gggcggatcacgaga | 8878 |
rs269446 | snp | C/G | 0.292266 | 0.246401 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833331 | TCATCCTCAGCACCT[C/G]TGCAGCCCCACTTAC | 8878 |
rs269449 | snp | C/T | 0.442385 | 0.15965 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834592 | accactccctaatct[C/T]aagtacccagggaca | 8878 |
rs269450 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834668 | tcaatggattaaggg[C/T]ggtgcaagatgtgct | 8878 |
rs272449 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | SQSTM1 | GRCh38.p7 | 5:179819415 | GAGAAAGCAAAGGAG[C/T]TCCTTCTTGGGGGTG | 8878 |
rs272450 | snp | G/T | 0.120326 | 0.21374 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179816880 | GGTCTCCGGCCACCC[G/T]GTGACGGAGGGAGGG | 8878 |
rs272451 | snp | C/T | 0.120674 | 0.21395 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179816795 | CTCCTTGTCGCCGCC[C/T]CCCCGTCTTTTCAGG | 8878 |
rs391355 | snp | C/G | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834259 | TGGGGGGTGGGGACA[C/G]CTGACAGAAACTCCT | 8878 |
rs401475 | snp | G/T | 0.097727 | 0.198275 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834620 | ggtgatgactcttaa[G/T]gagcatgctgccttc | 8878 |
rs401500 | snp | C/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834266 | GGGGGACACCTGACA[C/G]AAACTCCTCATTGTC | 8878 |
rs408369 | snp | A/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834361 | CTTCTCTGCCTTAGG[A/G]CAGGGGATGGCGAGC | 8878 |
rs440127 | snp | A/C | 0.100944 | 0.200705 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834624 | atgactcttaaggag[A/C]atgctgccttcaagc | 8878 |
rs449910 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835093 | ctcccggatggggtc[A/G]cggccaggcagaggc | 8878 |
rs475716 | snp | A/G | 0.459233 | 0.136827 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179822433 | TTGTGACAGATACAT[A/G]TGAGCTGAAATGGCT | 8878 |
rs478786 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835679 | agggagaccgtggag[A/G]aagagggagagggaa | 8878 |
rs478790 | snp | A/G | 0.497984 | 0.0316851 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179835680 | gggagaccgtggaga[A/G]agagggagagggaaa | 8878 |
rs480822 | snp | A/T | 0.151334 | 0.229706 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179829234 | CTGACTGCTGGGCCC[A/T]TTGCTCATTCGGGAT | 8878 |
rs499138 | snp | A/C | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179815581 | AATCCTGAGCAGATC[A/C]AAGCTTGATCCTCAG | 8878 |
rs502729 | snp | G/T | 0.499902 | 0.00698814 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179821774 | GAAACAGGGCTTCTG[G/T]GCCAACACCAACACT | 8878 |
rs513165 | snp | A/C | 0.496714 | 0.0404017 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179822073 | GTGTGAGAGCTTTTC[A/C]TCACCTTATAAACGC | 8878 |
rs513235 | snp | A/T | 0.494815 | 0.0506538 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179822099 | AACGCCATACATACC[A/T]TTTATCACCCTCTTA | 8878 |
rs515110 | snp | A/C | 0.18325 | 0.240924 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179822323 | TTTGTTTACCTGTTC[A/C]TTAGTTGACAGACAT | 8878 |
rs527602 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | SQSTM1 | GRCh38.p7 | 5:179824229 | CCATCCTGGCCACCC[A/G]AAGTGTCCGTGTTTC | 8878 |
rs528584 | snp | C/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179824095 | GCGTGCACAGAGGGC[C/G]TGCTCACCTCAGACA | 8878 |
rs529062 | snp | A/T | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179817844 | gtgaaacccatctct[A/T]ctaaaaatacaaaaa | 8878 |
rs546161 | snp | A/G | 0.418491 | 0.184691 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179827340 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 8878 |
rs546917 | snp | G/T | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179817811 | tgttggccaggatgg[G/T]cttgaactcctgact | 8878 |
rs565280 | snp | C/T | 0.418169 | 0.184985 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179826926 | ATCATGACCTCGGTG[C/T]TCCACTGTTTACCCT | 8878 |
rs567174 | snp | A/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179824439 | ATTGTAGGGCACCAG[A/G]AAGGTGGGGGGTATC | 8878 |
rs570120 | snp | C/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179824108 | GAGCCCACCCCAGGC[C/G]TGCACAGAGGGCCTG | 8878 |
rs693549 | snp | A/G | 0.417521 | 0.185571 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179831901 | CGATTCTTCTGCCTC[A/G]GCCTCCCGAGTAACT | 8878 |
rs695191 | snp | G/T | 0.41833 | 0.184838 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179830171 | atctagaagataatg[G/T]cctcattgccaagaa | 8878 |
rs1060271 | snp | A/C | 0.0563498 | 0.158113 | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837132 | TACAGTGGTGAAGAG[A/C]CCAGGAGGCAGCTCT | 8878 |
rs1065154 | snp | A/C | 0.46467 | 0.128128 | intron-variant, utr-variant-3-prime | C5orf45, SQSTM1 | GRCh38.p7 | 5:179837915 | GGCATTGTTCTTACA[A/C]ATGGAGGGCATGGCC | 8878 |
rs1137043 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179823416 | TTGCCATGAGCCGAA[A/G]TCACATGACTGTACT | 8878 |
rs1345579 | snp | G/T | 0.163892 | 0.234703 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179829923 | gggaagtgggggatg[G/T]tgtctccctatgttg | 8878 |
rs1872779 | snp | C/G | 0.497803 | 0.033074 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179818749 | GAAGTGGAAGGATTT[C/G]GGCTGCCCTCCCAGG | 8878 |
rs1960428 | snp | A/G | 0.148326 | 0.228391 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179830823 | catgcctgtaatccc[A/G]gcactttgggagacg | 8878 |
rs2161101 | snp | C/G | 0.487495 | 0.0780784 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179828970 | TGAACAGATGGTCTT[C/G]CTTCTCACCAGGATG | 8878 |
rs2241349 | snp | A/G | 0.478282 | 0.102006 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833009 | GGAACTTCACGGCTT[A/G]CTCTTTCCTCCTCCG | 8878 |
rs2241350 | snp | C/G | 0.256061 | 0.249927 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833478 | CCCCTGCAGCCTTAA[C/G]TGCACGTGTGCATGC | 8878 |
rs2306796 | snp | A/T | 0.00144389 | 0.0268302 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179822903 | TCTCAGCTGGACATA[A/T]GCTGCTGGAATGGGC | 8878 |
rs2431118 | snp | A/G | 0.472052 | 0.11486 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179831523 | aaaaattagctgggc[A/G]tggtggcacgtgcct | 8878 |
rs2434414 | snp | A/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179831507 | gcccagctaattttt[A/G]tatttttagtagaga | 8878 |
rs2450483 | snp | A/G | 0.120326 | 0.21374 | upstream-variant-2KB, intron-variant | SQSTM1, MGAT4B | GRCh38.p7 | 5:179804884 | TGTCACTGTTTCTGT[A/G]GTGACCCAGTAGTAC | 8878 |
rs2450484 | snp | C/G | 0.405255 | 0.195948 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179832842 | ACTGGCTGTGTGATT[C/G]CGGGGTCGAGCTGGG | 8878 |
rs2516294 | snp | C/G/T | 0.107807 | 0.206008 | intron-variant, upstream-variant-2KB | SQSTM1 | GRCh38.p7 | 5:179820747 | CTCTCCCCTTCCCCG[C/G/T]TACCCCTCGCTCCAG | 8878 |
rs2712962 | snp | C/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179815520 | TCAACTGGCTTAAGC[C/G]GTTTTATAACCCAGC | 8878 |
rs2890059 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | SQSTM1 | GRCh38.p7 | 5:179814339 | CCTCAGTGATGTACA[A/T]TCTCCAAAGACTGTC | 8878 |
rs3061754 | in-del | -/TT | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179826613 | TTTTTTTTTTTTTTT[-/TT]CTTTGAGACAGACTT | 8878 |
rs3061756 | snp | A/C | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179830129 | aaacaaaacaaaaca[A/C]aaaacaaacaaaaat | 8878 |
rs3061786 | in-del | -/AA | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179830134 | aaacaaaacacaaaa[-/AA]caaacaaaaatgcaa | 8878 |
rs3734007 | snp | C/T | 0.486067 | 0.0822953 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179825537 | GCAGACTATTGTTCA[C/T]CCAAAGGAGGGCAGT | 8878 |
rs3894460 | snp | A/G | 0.396694 | 0.202437 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834156 | GAGTGCTGGTCTGAG[A/G]GGGGGGGGGGGTCAT | 8878 |
rs4011593 | in-del | -/ATTT/ATTTATTT | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834430 | tttatttatttattt[-/ATTT/ATTTATTT]ttattgatcattctt | 8878 |
rs4011597 | in-del | -/G/GG/GGG | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834166 | TGAGAGGGGGGGGGG[-/G/GG/GGG]NTCATAGCCAAGATC | 8878 |
rs4333276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834660 | tttaacaaagcacat[C/T]ttgcaccgcccttaa | 8878 |
rs4700700 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, utr-variant-5-prime | SQSTM1 | GRCh38.p7 | 5:179821257 | CGTGAGGGGGTCTGC[A/G]CTGGCTGCTCCCTGG | 8878 |
rs4700842 | snp | A/C | 0.269267 | 0.249256 | intron-variant, upstream-variant-2KB | SQSTM1, MGAT4B | GRCh38.p7 | 5:179807522 | CAGGGGCGGCCCGAG[A/C]GCGCCGCTAACGGGA | 8878 |
rs5873666 | snp | A/C | 0.426703 | 0.176851 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179830135 | aacaaaacaaaacaa[A/C]aaacaaaaatgcaag | 8878 |
rs5873667 | in-del | -/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834157 | CTGGTCTGAGAGGGG[-/G]GGGGGGTCATAGCCA | 8878 |
rs6868381 | snp | A/G | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179825996 | TGCATCTCTCGCTAG[A/G]CGAGTGAGCTTGTTT | 8878 |
rs6877064 | snp | A/G | 0.245631 | 0.249962 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179811794 | acccccTTGGTCTCC[A/G]TGGCCTTTTCCTTAC | 8878 |
rs6880145 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, missense | SQSTM1, MGAT4B | GRCh38.p7 | 5:179806892 | CCTCCGCggcagggc[C/T]gggccgggccgggct | 8878 |
rs7378854 | snp | C/T | 0.49949 | 0.0159663 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179834664 | acaaagcacatcttg[C/T]accgcccttaatcca | 8878 |
rs7379611 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179831622 | agccgagagattgcg[A/C/G]cactgcgctccagcc | 8878 |
rs7379612 | snp | A/G | 0 | 0 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179831629 | agattgcggcactgc[A/G]ctccagcctgggcaa | 8878 |
rs7379685 | snp | A/T | | | intron-variant | SQSTM1 | GRCh38.p7 | 5:179809326 | accacgcctggctaa[A/T]ttttttttttttttt | 8878 |
rs7442857 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, missense | SQSTM1, MGAT4B | GRCh38.p7 | 5:179806839 | GCAGGTATCAGGCTC[A/G]CTGCAGATATCAGGG | 8878 |
rs7711505 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179823130 | GTAAAAAACAGGGCT[C/T]GATGTTCCACCAATG | 8878 |
rs7715234 | snp | A/G/T | 0.185267 | 0.254755 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179827604 | ATGTCTTTGAGCACT[A/G/T]AAAGCTAAAGGCTTA | 8878 |
rs7724957 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant, utr-variant-3-prime | SQSTM1 | GRCh38.p7 | 5:179813626 | ataataaaagccagg[C/G]atgttggcatgtacc | 8878 |
rs7735805 | snp | A/G | 0.0138096 | 0.0819396 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179833281 | GCCACCTGGGACCAC[A/G]GCCAGCCTAGTGATC | 8878 |
rs7736542 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SQSTM1 | GRCh38.p7 | 5:179827796 | AACTATAAGCTGGAT[A/G]ACTCACAGGTTAACT | 8878 |