SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs58035203 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379388 | CTATCTCAACAAAAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs58157029 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514044 | GCCCAGGCCCTTTTG[A/G]ATATTGGGTTCTTGG | 10580 |
rs58247371 | snp | C/G | 0.142609 | 0.225759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366437 | TATTTATCACATATA[C/G]AACAGGAGGTGAGGG | 10580 |
rs58282759 | in-del | -/AAA | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407970 | AAAAAAAAAAAAAAA[-/AAA]GACTATGTTGTCTCC | 10580 |
rs58294379 | snp | G/T | 0.219049 | 0.248077 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364440 | TAAATTGTGTGTGTG[G/T]GGGGGGGGGTGTTTG | 10580 |
rs58351234 | snp | A/G | 0.0153634 | 0.0862882 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356927 | TTCCTGCAAAAGAGC[A/G]CTGGGAGCAGAGAGC | 10580 |
rs58404187 | in-del | -/T | 0.137187 | 0.223099 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450230 | CACCTCGTATCCCTG[-/T]GCTTTAGGAGAATCT | 10580 |
rs58438919 | in-del | -/A/ATTA/ATTAT/ATTATTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342883 | ATTATTATTATTATT[-/A/ATTA/ATTAT/ATTATTA]TTTTTTTTTTTTTTT | 10580 |
rs58442707 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95437036 | TTTTAAAAACTGAAA[A/C]TATGAGAGGATGTGC | 10580 |
rs58484274 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408791 | TTATGATTAGTAATA[C/T]GGGGCTGGGCCAGTG | 10580 |
rs58497000 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469149 | GACATTTTCCTTTCC[C/T]TATCTTCCCCACCTT | 10580 |
rs58497671 | snp | C/T | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562757 | ACCACCTGGTGTCCT[C/T]TGCTGTGTATTAAAA | 10580 |
rs58503426 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403733 | TGTCCAGCTAATTTT[C/T]GTATTTTTAGTAGAG | 10580 |
rs58504068 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95402457 | TTTTTTTTTTTTTTC[C/T]AATTACACAGGGTCT | 10580 |
rs58507985 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537988 | CATGGTGGCTCACAC[C/G]TGCAGTCCAGTGACT | 10580 |
rs58512406 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467957 | GGCTGGAGTGCAATG[G/T]CATGATCTCATCTCA | 10580 |
rs58565168 | in-del | -/AA | 0.320814 | 0.239761 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392265 | CTCTTGAAATGGTTT[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs58671772 | snp | G/T | 0.046775 | 0.145601 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560089 | GGGGGCTGGGCGGGG[G/T]GGGGGGTGTTGAGGG | 10580 |
rs58672400 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370442 | GAGACTGGGTTTCAT[C/G]ATGTTGGCCACGCTG | 10580 |
rs58759119 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468115 | TTGTTCTGGCTGGTC[A/G]CGAACTCCCAACCTC | 10580 |
rs58762219 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466955 | AATATTGGAATATCA[C/T]GTTGTTCAAACTAAC | 10580 |
rs58783242 | snp | C/T | 0.255782 | 0.249933 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349185 | TGTTTGCATGTATCA[C/T]GTACATGTGTAAGTG | 10580 |
rs58892906 | in-del | -/TT/TTT | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366702 | TTTTTTTTTTTTTTT[-/TT/TTT]AGATGGAGTCTCACT | 10580 |
rs58992601 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385067 | GCTCTCCAAAGGCAT[C/G]ACACACATTCCTACG | 10580 |
rs58995358 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323105 | AGAGAGACTCAGAAA[A/G]GCCATCTTAGCCAGG | 10580 |
rs59097599 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375719 | GGGGGAGGTCTAAGA[C/G]AAGCAATGATTATTT | 10580 |
rs59127018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340179 | GCCATGTAGAGTGTT[C/T]GGATTCTGGAAAGAA | 10580 |
rs59127046 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375505 | ATCTGCACAAAGAGG[A/T]CCTTGTTGGCCTGCT | 10580 |
rs59255194 | in-del | -/CACA/CACACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452774 | ACACACACACACACA[-/CACA/CACACA]ATTTGCCTATATTAT | 10580 |
rs59286080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343029 | GGAGTACAGGCGCCA[C/T]GCCTGGCTAATTTTG | 10580 |
rs59295918 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95317597 | TAAATAAGGTCTTTA[A/G]AATGTCTACACGTAT | 10580 |
rs59354260 | in-del | -/GTTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373749 | TTTTGTGGCAGAGTG[-/GTTG]CAGTAGGAAGTGAAG | 10580 |
rs59361612 | snp | A/G | 0.284471 | 0.247612 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428203 | ATCATGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 10580 |
rs59368180 | in-del | -/AAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528942 | AAAAAAAAAAAAAAA[-/AAAAAAA]CTGTTTCCACAGTAC | 10580 |
rs59521949 | snp | G/T | 0.345037 | 0.231231 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536448 | ACAATGTTTTTTTTG[G/T]TTTTTTGGGGGTTTT | 10580 |
rs59660511 | snp | A/G | 0.121717 | 0.214577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409939 | ACCCAAAGAACTTCC[A/G]CTTCACCCCAACTCA | 10580 |
rs59705315 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560088 | GGGGGCTGGGCGGGG[-/C]GGGGGGGTGTTGAGG | 10580 |
rs59879351 | in-del | -/CACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502999 | ACACACACACACACA[-/CACA]AACACTCTGACCATC | 10580 |
rs59936054 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543661 | CTATCTTGAGCACTG[C/T]TTATCTACTGCTCTA | 10580 |
rs60044277 | in-del | -/T | 0.323671 | 0.238899 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551437 | AAGATCTACCGGCGC[-/T]GATATCTAGGCTGCT | 10580 |
rs60116861 | in-del | -/TA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318062 | ATAAATAAATATAAA[-/TA]AAATAAATGGAAACC | 10580 |
rs60166500 | in-del | -/C | 0.254105 | 0.249966 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512192 | GGAGGCCAAAGCAGG[-/C]AGATTACTTGAGATC | 10580 |
rs60184686 | snp | C/T | 0.137187 | 0.223099 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445488 | AGTGCAGTTCTCCAA[C/T]CTTCCATAAACTCCG | 10580 |
rs60186416 | in-del | -/T | 0.475702 | 0.107512 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386255 | ATTCAGGTTTTTTTG[-/T]TTTTTTTTTTTAAGC | 10580 |
rs60191443 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471128 | CATGCTCTATTATCA[C/T]TTCAGGGGCTACCAT | 10580 |
rs60236988 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547865 | ATGGGGCACCCCTAA[A/C]ACACTGTGAAAGACT | 10580 |
rs60290448 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452260 | CAAACACCATCTTTT[C/T]TGAGAAAACCTCTCT | 10580 |
rs60341341 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474767 | GCCCATGTTTGTGAA[C/T]AAACATGAGAACGTT | 10580 |
rs60400470 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511581 | GTTTTTGTCGTTGTC[A/G]TTTCTCAACATCAAA | 10580 |
rs60569518 | in-del | -/GCGCGCACACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358718 | CATGCGCGCGCGCGC[-/GCGCGCACACAC]ACACACACACACACA | 10580 |
rs60596642 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455610 | TAAAACTTTTTTTTT[-/TT]AACTTTACCACTTCC | 10580 |
rs60620060 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404881 | AGATAACCTGCCTGA[A/G]GCAGCACCAGACCCA | 10580 |
rs60688813 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536447 | CACAATGTTTTTTTT[G/T]GTTTTTTGGGGGTTT | 10580 |
rs60712346 | snp | C/T | 0.109108 | 0.206518 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424814 | TTTTACTTTTCTCAC[C/T]TATAAAATATAAGCC | 10580 |
rs60736089 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458647 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAGAAAA | 10580 |
rs60763329 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373007 | GCCAACTCCATGGAA[A/G]CATTCAAATTGGTTT | 10580 |
rs60841167 | in-del | -/GA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357397 | AGAGAGAGAGAGAGA[-/GA]AATCTTGAAGGAGAA | 10580 |
rs60844364 | snp | C/T | 0.155987 | 0.23165 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320066 | CTGGACAAAGTCCCA[C/T]ACTCTTGCTGCTTGG | 10580 |
rs60871127 | in-del | -/C | 0.0402882 | 0.136092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528801 | GCACATGCCTGTAAT[-/C]CCAGCTATTCAGGAG | 10580 |
rs60929816 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524218 | GGAAAAGGCAATGTG[C/T]GTCCACAATGACAAA | 10580 |
rs61029108 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353345 | GAGCTATAGAAATGA[A/T]TCTGCTCTATGGCCT | 10580 |
rs61051054 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490332 | TAGTGGTAGGAAGGG[-/A]AAAAAAAAAGAGAGA | 10580 |
rs61059073 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348453 | TCCTATCAATTAAAT[A/C]AATATAATTATATAG | 10580 |
rs61102040 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464839 | AAAAACACTGTTGGG[C/T]TTACTGTGTTGTGAA | 10580 |
rs61119394 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408813 | GGGCCAGTGAGGCTC[C/T]TCTCTTCTTCCTGAT | 10580 |
rs61238513 | snp | A/G | | | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394634 | TTAGGACTAGGAGTA[A/G]ATGCAGGAAACTGGT | 10580 |
rs61293457 | in-del | -/A | 0.435407 | 0.167703 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471031 | AAGACTCTGTCTTGG[-/A]AAAAAAAAAAAATCT | 10580 |
rs61345309 | in-del | -/GTTTATTTATTTATTTATTT/GTTTGTTTATTTATTT | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494874 | TTTATTTATTTATTT[lengthTooLong]ATTTATTTATTTGTT | 10580 |
rs61494027 | in-del | -/AAAAAAAAAAAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464345 | AGAAAAAAAAAAAAG[-/AAAAAAAAAAAAG]GCTCAAATTCAGGTA | 10580 |
rs61545469 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409304 | ATTTCACTTTGTCCC[A/G]CATTACAGACACTTT | 10580 |
rs61555606 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324005 | CAATAGGCCACAACT[A/C]CAGGGCCTTCTAGAT | 10580 |
rs61562616 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371729 | CTATTTTCTCTTTTT[C/T]CAGAGTGTGGTGACA | 10580 |
rs61571952 | in-del | -/AT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358748 | CACACACACACACAC[-/AT]ATTTCTCAGTTAAGT | 10580 |
rs61574729 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325568 | CTTTTTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 10580 |
rs61588313 | snp | A/G | 0.432651 | 0.170701 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358720 | TGCGCGCGCGCGCGC[A/G]CGCACACACACACAC | 10580 |
rs61625286 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324004 | GCAATAGGCCACAAC[A/T]CCAGGGCCTTCTAGA | 10580 |
rs61641116 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343291 | TCTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 10580 |
rs61676390 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407672 | GGCCAGGCACGGTGG[C/T]TCATGCCTATAATCC | 10580 |
rs61738262 | snp | C/T | 0.027392 | 0.113779 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559375 | TATGCCCAATCTCTT[C/T]CGAAAAGTATACAGA | 10580 |
rs61739184 | snp | A/G | 0.0750103 | 0.178546 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95381730 | GCCAGGCTGATATTC[A/G]TAAATGCTCTTGGGC | 10580 |
rs61739185 | snp | C/T | 0.0104326 | 0.0714663 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95315104 | TGGAAAAGTACCAAA[C/T]TGCTTTGTCCTTCTT | 10580 |
rs61739187 | snp | C/T | 0.0119027 | 0.0762211 | missense | SORBS1 | GRCh38.p7 | 10:95315108 | AAAGTACCAAACTGC[C/T]TTGTCCTTCTTGAAG | 10580 |
rs61739253 | snp | A/G | 0.00601268 | 0.0544994 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357740 | CTCATTCTCCAAGCT[A/G]GTGAGATCCCCAGGA | 10580 |
rs61868660 | snp | A/G | 0.00054742 | 0.0165351 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355820 | GCGTGTGGGAACCAC[A/G]GGCTTCCCCCCAGAA | 10580 |
rs61868661 | snp | A/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358726 | CGCGCGCGCGCGCAC[A/G]CACACACACACACAC | 10580 |
rs61868662 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361589 | TAGCTGGGACTACAG[G/T]TGCCTGCCACCAAGC | 10580 |
rs61868663 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362574 | CCCCTTCTCTCTCTC[C/T]CCTTGCTCCTTAAGC | 10580 |
rs61868664 | snp | C/T | 0.381697 | 0.212499 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365062 | GCACAGGACCTGGCA[C/T]GTAGTAAATGCCTGA | 10580 |
rs61868666 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400868 | GAAAAAAAAAAAAAA[A/C]CCCCAGAAATTGAAG | 10580 |
rs61868667 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400872 | AAAAAAAAAAAACCC[A/C]AGAAATTGAAGCAGA | 10580 |
rs61868669 | snp | C/G | 0.0519815 | 0.152606 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415995 | ACCACACCTTTGGGA[C/G]CCGATCCAGCTGCCA | 10580 |
rs61868670 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429620 | ATCTTAAATTTATCA[C/T]CAATCAAAGGGATTC | 10580 |
rs61868671 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443231 | GAAGGCCAAGATGGG[C/T]GGATCACCTGAGGTC | 10580 |
rs61868672 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450017 | AATAAACAAATCTAT[A/G]AGAAAACGTTTACTT | 10580 |
rs61868673 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466439 | AGCAAGACTCCATCT[A/C]CAAAAAAAAAAAAAG | 10580 |
rs61868674 | snp | C/T | 0.309154 | 0.242901 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477214 | CCTGTTCCTTCCTTT[C/T]GTCTCTGACCTAGGG | 10580 |
rs61868704 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95478196 | TGTTTCCACCTCCAC[A/C]AACTATGAGAATGAT | 10580 |
rs61868705 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478736 | CATTTATAACCACAG[C/T]TCCCTGGCACCACAC | 10580 |
rs61868706 | snp | G/T | 0.272511 | 0.248984 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480142 | AGCCAGGAGGGGACG[G/T]GCTGAAGCAAAAGAC | 10580 |
rs61868708 | snp | C/T | 0.294832 | 0.245947 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498752 | TTTCAAGCTCCTAGG[C/T]TCAAGCGATCCTCCT | 10580 |
rs61868709 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503016 | ACACACACACACACA[A/C]ACACTCTGACCATCC | 10580 |
rs61869969 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517302 | CTGCAAGAGGATTAA[C/T]TGCCTCCTAAAGGAC | 10580 |
rs61869970 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517365 | GGATGGCACAAGAGT[C/T]GGGTCCGGCCCTCAC | 10580 |
rs61869971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519360 | GCTGCCACCAGCACC[C/T]GTGAATGTTACCACC | 10580 |
rs61869972 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520593 | AGTAAGCCGAGATCT[C/T]GCCACTGCACTCCAG | 10580 |
rs61869973 | snp | A/C | 0.217851 | 0.247924 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523141 | CTAAGTAAAATACTT[A/C]AGCAAGGAAAAGCAA | 10580 |
rs61869974 | snp | C/T | 0.21845 | 0.248001 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523568 | AGTTTTTAAAAAATA[C/T]ATTTAGCACATGGTT | 10580 |
rs61869975 | snp | C/T | 0.220843 | 0.248294 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524872 | GAGTAAATGTATACA[C/T]TGGCATCACTAATGA | 10580 |
rs61869976 | snp | A/G | 0.21875 | 0.248039 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525210 | GGGAAACAGAGAAGG[A/G]TGCCATCCTGACCAC | 10580 |
rs61869977 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530079 | CCTGCAGGGCAGGGA[C/G]TGGGTCCCATCCATC | 10580 |
rs61869978 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533799 | TCACGGCCACATGAC[A/T]GGCCGTCCCGCTCTC | 10580 |
rs61869980 | snp | C/T | 0.233235 | 0.249437 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538066 | GCAGTGAGCCATGAT[C/T]GCACCACTACACTGT | 10580 |
rs61870045 | snp | A/G | 0.289683 | 0.24683 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544382 | CATCACCCCTAACCC[A/G]TGGACCCCCATATCA | 10580 |
rs61870046 | snp | A/C | 0.323434 | 0.238972 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544975 | TAGGGGGCCTCGCCC[A/C]CTCACACCTGCCATT | 10580 |
rs61870048 | snp | A/C | 0.323671 | 0.238899 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554309 | TCCGCCCACCTCAGC[A/C]TCCCAAAGTGCTGGG | 10580 |
rs61870049 | snp | C/T | 0.323671 | 0.238899 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554329 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 10580 |
rs61870050 | snp | A/G | 0.323908 | 0.238825 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554378 | TTCAAAACTCTGTGC[A/G]GGGTGGGGGTGCACA | 10580 |
rs61870051 | snp | C/T | 0.319136 | 0.24025 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556759 | TTTCACCATGTTGAC[C/T]AGGCTGGTCTTGAAC | 10580 |
rs61870052 | snp | A/C | 0.324145 | 0.238752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556943 | TGTTGATAATAAAGA[A/C]AGAATGAGGGAGGAG | 10580 |
rs61871383 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323507 | TAACATAGAAACACA[A/G]GTGCAAACATGGCCA | 10580 |
rs61871384 | snp | A/C | 0.5 | 0 | missense | SORBS1 | GRCh38.p7 | 10:95339252 | TGATGGGGAAGATGC[A/C]TTGTCGGGATGTCCC | 10580 |
rs62621366 | snp | A/G | 0.0021702 | 0.0328693 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355431 | AAACACAGTTTGGTG[A/G]TTAGTCTAAATGACA | 10580 |
rs62625036 | snp | C/T | 0.00788994 | 0.0623115 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395073 | GGTTTTCTTCAGGAG[C/T]GTCTAGGCAGAGGAG | 10580 |
rs62625037 | snp | C/T | 0.000629366 | 0.0177281 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356649 | GATCGGTTGATCTGG[C/T]GCATGTCCCGATAAA | 10580 |
rs62993261 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361613 | ACCAAGCCTGGCTAA[A/T]TTTTTTTTTTTTTTT | 10580 |
rs66522177 | in-del | -/ATTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510799 | AGACTCTGTCAAAAA[-/ATTT]TTTTTAAAGTGGAAA | 10580 |
rs66674085 | multinucleotide-polymorphism | AAAAAA/CAAAAC | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499082 | GTCTAAAAAAAAAAA[AAAAAA/CAAAAC]AAAAAAAAAAACATT | 10580 |
rs66761269 | in-del | -/AT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358704 | CGCACATGCACAGAC[-/AT]GCGCGCGCGCGCGCG | 10580 |
rs66881330 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390634 | CCTAACTATATATTC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs67008126 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395652 | GCTTCCAAAGCTGGG[A/T]CTAAAGGTGAGAGTC | 10580 |
rs67201255 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350899 | GCACAGGCAACACAG[A/T]AGCATGATAAAATGC | 10580 |
rs67435718 | in-del | -/AGA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445066 | GGATGCTGAGAGGGT[-/AGA]AGGAGAATGGACCCT | 10580 |
rs67753497 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383433 | TTTCTTTTTCTTGAG[-/T]TTTTTTTTTTTTTTT | 10580 |
rs67824526 | in-del | -/AG/GA | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325559 | AAAAAAAAAAGAAAA[-/AG/GA]AAAAAGAAGTAGTGC | 10580 |
rs67832614 | snp | C/T | 0.171704 | 0.237423 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403545 | CCTGAGCTGCCAGCA[C/T]GGTGGAGCCACCCTC | 10580 |
rs67857865 | snp | A/G | 0.242201 | 0.249878 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370697 | CTCTTACTCTCTCTC[A/G]TATACCCTTTAATAA | 10580 |
rs68023943 | in-del | -/TT | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428431 | TCTTTCTTCTTCTTC[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs68133374 | in-del | -/AG/GGT/GTG | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432334 | TCTTGGGGGGGGGGG[-/AG/GGT/GTG]GTGTGTGTGTGTGTG | 10580 |
rs70937021 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314049 | CCAGGGTTTGCCGTG[A/G]CTCCAGATCTACTCC | 10580 |
rs70937022 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312741 | ACAGCTAGAAAATAA[A/G]ACCAATTTGTAAAGC | 10580 |
rs70937023 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312448 | CAACACATTTTGATA[C/T]ATTAGCCATGCTTCC | 10580 |
rs70937024 | snp | A/G | 0.00562894 | 0.0527521 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441184 | GGTGTTTGTTTTTCT[A/G]CAGAGCAGTTCAGAG | 10580 |
rs70937025 | snp | A/G | 0.00109627 | 0.0233866 | synonymous-codon, splice-acceptor-variant, intron-variant | SORBS1 | GRCh38.p7 | 10:95414656 | TCCCCCTCATCTGCA[A/G]AGGTGGCCCCACCAC | 10580 |
rs71034335 | in-del | -/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551352 | GGGGTAGGGTGGGGT[-/G]GGGGTGGTAAACAGC | 10580 |
rs71274292 | in-del | -/AAAAAA | 0.356597 | 0.226135 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548449 | AAAAAAAAAAAAAAA[-/AAAAAA]GGAAAGAAAAGAACT | 10580 |
rs71306814 | in-del | -/TT | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414000 | TGACAGAGACTAGGA[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs71306815 | in-del | ATCTC/GTTGAGAT | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406229 | CAGTGAGGACTCAGG[ATCTC/GTTGAGAT]CCTAACGAGTTATGC | 10580 |
rs71482352 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327055 | CTAGACAATGCCTCT[C/T]TGAGCCCTCCCCAGG | 10580 |
rs71482353 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370249 | TCCATATTCCTTTTG[G/T]ATCTTTTTTTTTTTT | 10580 |
rs71482354 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390268 | CCTGGACTCGCCTTC[C/T]CACTGACATGGTCCA | 10580 |
rs71482355 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401051 | ACAGAGGAAGGAATG[C/T]ACTAGATGGTAATTC | 10580 |
rs71482357 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453759 | TGGATCAAAAATATA[C/G]CATTTGTAGGATGTG | 10580 |
rs71482358 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456696 | GGTTGGGCCACAAGA[A/G]GGGCAGTGGTGCCCA | 10580 |
rs71482359 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460967 | TAACATTGGGTCTCT[A/G]TCTTCGTCCCTTTTT | 10580 |
rs71482360 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531461 | CCTGATTCTTTCTTG[G/T]GTTTATTATGTTCAG | 10580 |
rs71482361 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532934 | AGATTTCCAGTGTAT[C/T]GGTTCTTCTTTGTCT | 10580 |
rs71482362 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540558 | TGGTAGGCATACTAG[G/T]TATTCAAAAACATAT | 10580 |
rs71483997 | multinucleotide-polymorphism | AAC/CAG | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388972 | AGAACAACTTTCAAC[AAC/CAG]TACTTTCTTCAGTTG | 10580 |
rs71483998 | multinucleotide-polymorphism | CGCGCGCGCGCGCGCGCAT/TGTGTGTGTGTGCGCGCGC | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358704 | GTGTGTGTGTGTGTG[lengthTooLong]GTCTGTGCATGTGCG | 10580 |
rs71486755 | in-del | -/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366666 | TTAGCCCCTTCTCGG[-/G]CACCTCCCTCCCCCC | 10580 |
rs71486756 | in-del | -/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367228 | TTTTTTTTTTTTGGG[-/G]TAGAGACAGGGTCTA | 10580 |
rs71486757 | in-del | -/A | 0.0178168 | 0.0926875 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422771 | AAAATCTAATCACCC[-/A]TTCCTGAGTGTTCAT | 10580 |
rs71486758 | in-del | -/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429427 | CGGCCTCCCAAAGCG[-/C]TGGGATTACAGGTGT | 10580 |
rs71486759 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499092 | TTTTTTTTTTTTTTT[-/TT]AGACGGAGTCTGGCT | 10580 |
rs71486762 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534663 | ATTTTGGCTTTTTTT[-/T]CCCCATTCAATAAGT | 10580 |
rs71486763 | in-del | GG/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560094 | CTGGGCGGGGGGGGG[GG/T]TGTTGAGGGGAGAGA | 10580 |
rs71486764 | in-del | -/AAAA/AAAAA/AAAAAA | 0.469445 | 0.119766 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562768 | CCTCTGCTGTGTATT[-/AAAA/AAAAA/AAAAAA]AAAAAAAAAAAGAAG | 10580 |
rs71677080 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349829 | TCTTCCCAGACACAT[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs71799146 | in-del | -/ACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503005 | ACACACAAACACACA[-/ACAC]CACACACACAAACAC | 10580 |
rs71884769 | in-del | -/AAAAA | 0.497722 | 0.0336691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383416 | GCAAAACTCCGTCTC[-/AAAAA]AAAAAAAAAAAAACT | 10580 |
rs71992595 | in-del | -/GA | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393437 | ATGATGAGAAGGGCT[-/GA]GAGGGATGGTCTGCT | 10580 |
rs72071061 | in-del | -/GTAGGGAG | 0.273318 | 0.24891 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419424 | ATGCTGATAATGGCA[-/GTAGGGAG]GTAAGCAAAAGATCA | 10580 |
rs72164932 | in-del | -/T | 0.28578 | 0.247426 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332252 | ACACCCTGCCTGGCA[-/T]TTTTTTTTCCTGAAG | 10580 |
rs72198283 | in-del | -/A | 0.49823 | 0.0296997 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563191 | CATTTTAGAATAGCC[-/A]AAAAAAAAAAAAATC | 10580 |
rs72213123 | in-del | -/GT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378736 | CGTCCTACTACATAT[-/GT]ATGTGTGTGTGTGTG | 10580 |
rs72264932 | in-del | -/TGGT | 0.491629 | 0.0641526 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373747 | TCTTTTGTGGCAGAG[-/TGGT]TGCAGTAGGAAGTGA | 10580 |
rs72637509 | snp | C/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442526 | TGGCACCCCCCCCCC[C/G]CACCCTTACTTATGC | 10580 |
rs72809755 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524840 | GGCACATAATGGGCA[C/T]ATAATAAACATCTGG | 10580 |
rs72809757 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525958 | ATGGAAGAACTAAAG[A/G]GGCTTAATATGGAGC | 10580 |
rs72809762 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534397 | ACGAGCCACCGCGCC[C/T]GGCCCATGCAGCTCC | 10580 |
rs72809764 | snp | A/C | 0.0770498 | 0.180522 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535616 | AAACTGATAAAAGTA[A/C]CTACCTATCTGTTGG | 10580 |
rs72809780 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559837 | TGTAGACAGCCATCT[A/G]CCTCATCGGTGTCTG | 10580 |
rs72822520 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318061 | AAATAAATAAATATA[A/T]AAAATAAATGGAAAC | 10580 |
rs72822521 | snp | A/C | 0.240765 | 0.249829 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319966 | GGCCCTTTAACTCCC[A/C]CCATGGCTGCTTTGC | 10580 |
rs72822522 | snp | A/G | 0.240478 | 0.249819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320133 | ACTCCTCAGAACATT[A/G]TCCCATGGGGTCCTT | 10580 |
rs72822524 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326444 | TCCTGAGAGGTAGGG[A/T]TGACTGGGTGCCTCA | 10580 |
rs72822525 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326765 | TTACAGCTTTGTACA[A/G]TGCTTCTTCTGGACC | 10580 |
rs72822526 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327370 | TATTTGTACACAAGT[C/T]GCCTCTCCTGGCCTG | 10580 |
rs72822527 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329518 | GGCCAGTTCCCTACC[A/G]TTAGTGATGAGAGAA | 10580 |
rs72822529 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329934 | CATAGCTTTCCAGTA[C/T]ATTGAGATTTTATTT | 10580 |
rs72822531 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331861 | CATTTAAAGCAGGCA[C/T]CTGGTCCCAGATTTC | 10580 |
rs72822532 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332133 | TGCACCCTTTTGCAG[C/T]GTTCTTTCTTTCTAA | 10580 |
rs72822533 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333206 | TAAAAGGAACATTTA[C/T]CATCTATTCTCTCCG | 10580 |
rs72822534 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333415 | ACCCCATTGGTTGGG[G/T]CTTCATTCTGAAGGC | 10580 |
rs72822537 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339048 | TGCTCAAAAACCTCC[C/T]CAGAGAGGCTGTGTG | 10580 |
rs72822540 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350239 | AATATTAATCTACTG[C/T]ACTGAAAGGTTATAA | 10580 |
rs72822541 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352516 | AGTGACAACTCATCA[A/T]ATGGCTGTGGGATTT | 10580 |
rs72822542 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358153 | GAGGATCACACATAG[A/G]GGAGGGCAGGAGGAC | 10580 |
rs72822547 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360350 | ACACCTCCTTAAGCA[C/T]TGGAGATCAGTAAAC | 10580 |
rs72822548 | snp | A/G | 0.234692 | 0.249531 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364546 | CAACCTCCGCTTCCC[A/G]GGGAAGCAATCCTCC | 10580 |
rs72822550 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370078 | CCCCGGTCTCTTCAC[C/G]CCTTCCCTGGTTTGA | 10580 |
rs72822551 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371680 | TATTCTACTTGCTAC[A/G]GAGAACTACAAAAAC | 10580 |
rs72822552 | snp | C/G | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374564 | GCAAAAGCTTTTTTC[C/G]GTGACATAATTGACC | 10580 |
rs72822553 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375117 | TCCAATGCATAAAGT[C/G]TCATACAATCATTGA | 10580 |
rs72822554 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376310 | GAGGAAAATGGACTA[C/T]AGATGGACAACTCTG | 10580 |
rs72822555 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378042 | GGGTGAGAGCAACCA[G/T]CCTCAGTCCTTTGAG | 10580 |
rs72822557 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378896 | TCTCCAATTCCAAGG[C/T]TAGAAGAGAAAAAAG | 10580 |
rs72822558 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379111 | AGCTGGGCCAGGCAC[A/G]GGCTCATGGCTGTAA | 10580 |
rs72822559 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379736 | ACCCACAGTTAACAA[C/T]GGAAGTGTGTGTTTT | 10580 |
rs72822562 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387906 | AGTTTTCTGAGTTGC[C/T]TCACATTTCTAGTTT | 10580 |
rs72822563 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392204 | CCTGCTGGAGCTCAC[A/G]GACAACATGAAAACC | 10580 |
rs72822564 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392386 | CATCAGTGATCTATG[C/T]CCGGATATGTCATCT | 10580 |
rs72822565 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395760 | AGCATTTAGTTTCAC[C/T]ACTGTGACCACGCTC | 10580 |
rs72822567 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395868 | AAACAGTTTGAACAG[A/G]GGCACACCCAGGTTC | 10580 |
rs72822568 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396496 | GGGACTCAATCCAGG[A/T]GAGAACATTTTTTTT | 10580 |
rs72822570 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402292 | AAAGTGTCACTTTAC[A/G]TAATGAAAACCCAAA | 10580 |
rs72822571 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404400 | CAGCTGTTCAGAAAA[C/G]AGTGGCTTTTGTTAT | 10580 |
rs72822572 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405256 | CCAGCCTTGGCAACA[C/T]AGTGAGACTCCAGCT | 10580 |
rs72822574 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405934 | TGGTCTGTCCACCAC[A/C]CTGCAAGCTCCAGGG | 10580 |
rs72822577 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408343 | TTTTCATCCTGAGAG[A/T]TTTCTGATTCAAAGC | 10580 |
rs72822580 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410979 | GTATTAGTATGGGGC[A/G]GAGGAGAGAGAGAAG | 10580 |
rs72822582 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411483 | AATCTGCATATTGGG[A/G]ATAATGCCAGTCTTT | 10580 |
rs72822586 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415349 | GAAGAATTCGGGACT[A/C]AAGCCACAACAACAT | 10580 |
rs72822587 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416969 | TTGGCCTCTACCGGA[C/T]TGGACTGTGCCTAGT | 10580 |
rs72822592 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420752 | ATTCCACGCTGAGGA[C/G]GATAAGCATCTGTAG | 10580 |
rs72822593 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421118 | GCTTCAGTGGGCTAC[A/G]ATGACACCATTGCAC | 10580 |
rs72822594 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423473 | AGGGCTGTACAAAAA[A/G]AGGCACAGGCCAGAT | 10580 |
rs72822595 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426750 | TTTTTTAATCTGTAT[C/T]CTTTCCCTACAATAA | 10580 |
rs72822598 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428444 | AAAAGAAGAAGAAGA[A/C]AGAGCTCATTTAATC | 10580 |
rs72822599 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428934 | TCCCAGTCCAGACTG[C/G]GCTTGGCTGTCTGCA | 10580 |
rs72824506 | snp | A/G | 0.230896 | 0.249269 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442625 | AGAAGCCAAGCAGAT[A/G]CTTCCTGTACAGTTA | 10580 |
rs72824518 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455872 | GCCTGGGTGGTCGAG[A/G]CTGCAGTGAGCCATG | 10580 |
rs72824540 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491619 | ATAGGCAGGCTTGGC[C/T]GCTCCAATATACCAC | 10580 |
rs72824551 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503916 | ATCTTAATTATTACT[G/T]ATCACGGATTGGAGC | 10580 |
rs72824552 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505557 | GATGAATGTCTAACA[C/T]AAGAGTCAATTCAAA | 10580 |
rs72824561 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508653 | ATCCAACAATGGAAA[C/G]AGTGGCTCCTAGAGA | 10580 |
rs72824564 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508895 | AGAAGGGCCATAAAT[A/C]GAGAGACAAAGGGCA | 10580 |
rs72824576 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517201 | TTGTTGTTGAACTCC[C/T]AAAGTAGAGGCCATA | 10580 |
rs72824578 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519398 | TGTCCCCACTAAGAG[C/T]GAGCACAGACACCCC | 10580 |
rs72824580 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523925 | TCCACTTTTTGATGT[G/T]GCTCCAACTTTTCTT | 10580 |
rs72824582 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523932 | TTTGATGTGGCTCCA[A/T]CTTTTCTTTTGACAA | 10580 |
rs73319222 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320009 | TGGGAAATAACTCCA[A/G]TATCTGCTTCTCTAT | 10580 |
rs73319229 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328781 | TTAGGTGGAACAGGG[C/T]AAGGTGGATAAAGTA | 10580 |
rs73319245 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359239 | TTCAATCCTAACATT[A/C]CTACTTCTGCCATTT | 10580 |
rs73319247 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363109 | AAAGCTTAACCTTTC[C/T]TCCTCCACAAAACAA | 10580 |
rs73319253 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367235 | TTTTTTGGGTAGAGA[C/T]AGGGTCTATGTTGCC | 10580 |
rs73319257 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372242 | AGCCTGAGGATTTGG[A/G]AGCTGGGACTGTTAC | 10580 |
rs73319268 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381133 | CTTAGAGATGTAAAC[A/T]TGTATAGGGAATCAT | 10580 |
rs73319270 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382288 | CTCAGTTTCCTCATC[C/T]GAAAAATGGGGTTGT | 10580 |
rs73319274 | snp | C/T | 0.014635 | 0.0842813 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384275 | GGGAGAGTACAGATC[C/T]GAATCATCATCTATT | 10580 |
rs73319275 | snp | A/G | 0.020082 | 0.0981719 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384392 | CATCCAGCCCCCCTA[A/G]GGATCCCAGCGGACA | 10580 |
rs73319278 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386062 | TAGTTAGAAGCTGAT[A/G]TATGCACTGCTTAAA | 10580 |
rs73319288 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391046 | TGCAGTCAGATACCA[G/T]AGAGCCTCTGGACAA | 10580 |
rs73319301 | snp | C/G/T | 0.0260348 | 0.111246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401114 | AAGCTGGCTGGGTGC[C/G/T]GTGGCTCATGCCTCT | 10580 |
rs73321203 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402185 | TGTCCTTTTGATCTA[C/T]AAAATTTAGCCCTGA | 10580 |
rs73321218 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409492 | AAACTACTAAAACAA[A/C]CTTAAGATTTTAGTG | 10580 |
rs73321220 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410182 | TGTCTACACAATATG[C/T]TTTCTTTTTTAAATT | 10580 |
rs73321221 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414181 | CACCACACGACCCCC[A/G]ACCTGGCCTGTGAAA | 10580 |
rs73321222 | snp | A/T | 0.0061061 | 0.054916 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95416018 | AGCTGCCAGGAGGAC[A/T]GAGATAGGCTGGGGT | 10580 |
rs73321224 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416408 | GAGAGGTAGGCCTGA[C/T]TCTCCTTTGTATCCA | 10580 |
rs73321228 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420725 | CATACAAGGCAGACA[A/G]TTAAGCAACCAATTC | 10580 |
rs73321231 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425624 | GATCCTTAGGGATAG[A/T]TCCACTTTTTCTTCT | 10580 |
rs73321233 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427211 | CTGGCATCTAAGTCA[A/G]AACACAGGAATTGAT | 10580 |
rs73321234 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427319 | TCTGGAGTGAAAACA[C/G]CCTGACCTGGGACAT | 10580 |
rs73321237 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429537 | CTTAATGAGCACGTG[G/T]ATTTTTTCTTTGTTT | 10580 |
rs73321239 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430268 | GTTCAACATCAACCT[A/G]GGCAACATGGAGAAA | 10580 |
rs73321240 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430962 | ACCAGAAAGGGGTTT[A/G]TGCTCAAACCCTAGC | 10580 |
rs73321241 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431200 | TTCCATTTCTCCCTC[C/T]CTTTCCTTCAAGAAA | 10580 |
rs73321243 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431605 | TGCCACCAGGCATGA[C/T]ACACAGCACTTCATA | 10580 |
rs73321245 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433689 | TTTCCTTTCCTTCCA[C/T]GCCAGCAGCCCCCTG | 10580 |
rs73321246 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437309 | GCAGCCTCAGACTCC[C/T]GAAATGCAACAACAG | 10580 |
rs73321253 | snp | C/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441694 | CACAGATGAGGAAAC[C/G]GAGACACAGACAGGT | 10580 |
rs73321259 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446918 | GCACCTTGGGAGGCC[A/G]GTGCTTGAGGTCAGG | 10580 |
rs73321260 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447395 | GTCACTTGGACCCAG[A/G]AGGCCTCAGAGGTTG | 10580 |
rs73321262 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452573 | TAATGAGTTTTCTTC[A/C]AACCAAGATAAAACC | 10580 |
rs73321267 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456474 | GCCCTCACCAGATGC[A/G]ACCCCTCCATAATCT | 10580 |
rs73321275 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459602 | CTGGAAAAGCCCTTC[C/G]TTGGAGTCACCCAGC | 10580 |
rs73321280 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460134 | AAAAGGAGACCAATG[C/T]GTCCCAGCCCAAACA | 10580 |
rs73321299 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470698 | TCTTGACATCGCCTC[C/T]ATGTCCTGCTGCATT | 10580 |
rs73323105 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473784 | AAGAGAGGTACCTAG[A/G]TCCTAGATATGAGAG | 10580 |
rs73323107 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477375 | CTTGGGGAGTAGGAG[A/T]GGGAATAAGTTCTGG | 10580 |
rs73323112 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482174 | GCCCACAGCAAAACA[A/C]CCCCTGCAGCCTCCA | 10580 |
rs73323115 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483364 | ATTTGTATAAATGTT[A/C]CCAACATGGTATTTT | 10580 |
rs73323119 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484948 | CACTGCACTCCAGCC[A/G]GGACAACAGTGCGAG | 10580 |
rs73323126 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495188 | CCGCACCCGGTGGTG[G/T]TCCTCAATTTTTAAA | 10580 |
rs73323128 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495443 | ACCCGACCCACTCTG[A/G]ACCACTCTGGGCTCT | 10580 |
rs73323156 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517128 | CCTAATACTGACCTT[C/T]CAGGGTTGAGAGGAT | 10580 |
rs73323159 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520835 | GAATGCAGAAAGACT[A/G]AGAATCTAATCTATT | 10580 |
rs73323173 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527671 | TAGAGAGGCGGCACT[C/G]TATGAATCCTTCTTG | 10580 |
rs73323194 | snp | A/G | 0.186105 | 0.241697 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541263 | AGATCACAACTGGGG[A/G]TTAGAAGAGGGATCT | 10580 |
rs73323197 | snp | C/G | 0.185788 | 0.241613 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541314 | GTCCCCACTCACGCC[C/G]TCTTTCCCCAACAGC | 10580 |
rs73325119 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550899 | ATTTAGGTTTCCGCA[C/T]TGTCTGCTCTGCTAA | 10580 |
rs73325125 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555161 | GTGCTGGGATTACAG[C/T]TACCGCGCCCAGCTG | 10580 |
rs73325127 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557665 | CAGGAGCAATCCCAA[A/G]GAGATTCCAAGACAG | 10580 |
rs73325138 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559251 | GACTCTGCTATCTGT[A/T]TTGAACTCTTATTTT | 10580 |
rs74150904 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383017 | ATTAATTTGTCTGTG[A/T]GGTTGGAAAAGGTAG | 10580 |
rs74150908 | snp | G/T | 0.137187 | 0.223099 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445567 | CCAGAGGTGGTTTCT[G/T]GTTATCTGCCACCCA | 10580 |
rs74150909 | snp | A/T | 0.0887219 | 0.191022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459239 | ACTTACTAAAAACAG[A/T]AATAAAAAACACTTG | 10580 |
rs74150918 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500048 | CCACTGAAACTATAG[C/T]TCTATTTAGTAAGGC | 10580 |
rs74150919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501587 | AAGCCAGGCATGGTG[A/G]TGTGGGTCTGTAGTC | 10580 |
rs74150922 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515863 | GGCCTAACGCACCCT[A/G]TGAGAGAGGTACCTT | 10580 |
rs74150926 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530323 | TTAGTACTTATCACA[A/C]AGCTTTGTAATCATC | 10580 |
rs74150942 | snp | C/T | 0.300673 | 0.244811 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560648 | AGATGCTGTCAGCCA[C/T]TCGGGGAGAAGAAGG | 10580 |
rs74231388 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483240 | AGTTTTATATTTTTG[A/T]CTATTAAAAGGAAAA | 10580 |
rs74331457 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341220 | GTGATAGCAACACCA[C/T]GCTTCCCCACATAGC | 10580 |
rs74340277 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432743 | TCTGTGGGTGGTGGA[A/G]AGGGGCAAGTTTTCA | 10580 |
rs74368353 | snp | C/G | 0.0043762 | 0.046572 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441079 | GGAAATCTGGGTAAA[C/G]TGCCCAGTTTGGTAG | 10580 |
rs74380223 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409631 | TCCCATTCTCATTCA[A/G]ATTAATGCAGAGAGG | 10580 |
rs74390410 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364443 | ATTGTGTGTGTGTGG[C/G/T]GGGGGGTGTTTGCTT | 10580 |
rs74398622 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559914 | TGACCCCTCTGTGTC[C/T]ACCCCACTTTTAATC | 10580 |
rs74434576 | snp | C/G | 0.0618563 | 0.164627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354201 | GATATGAAGAACTTC[C/G]TCTTCCCAAATCCCC | 10580 |
rs74436646 | snp | G/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442439 | GTTTGGATCATGGGG[G/T]TGGATATCTCATGGC | 10580 |
rs74438456 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463177 | AACAAATATGCCAAG[C/T]GCTCATGGAGTGTCT | 10580 |
rs74487488 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536439 | GAAGTAGGCACAATG[G/T]TTTTTTTGGTTTTTT | 10580 |
rs74502968 | snp | A/G | 0.161596 | 0.233848 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507278 | TCACAGGTGGGTGAG[A/G]ACTTGGGAAGGAATA | 10580 |
rs74542804 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315566 | AAAGCCCACTGACTA[C/T]GGCCACCCATCAAAA | 10580 |
rs74546941 | snp | C/T | 0.0132317 | 0.0802544 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356328 | TCCATCTCCTTGGGA[C/T]GGAGCTTGGTTGACT | 10580 |
rs74580868 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522818 | CTTTGCCCACAGTCA[C/G]ACAGCAAGTTAAGAA | 10580 |
rs74591537 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323145 | ACATATTGGTCCCCT[C/T]ACGCTCAGCTAGTAA | 10580 |
rs74652897 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511894 | GCCCTCTAAGAAGGG[C/T]CTTCTCCTTTTTCTG | 10580 |
rs74655665 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534758 | AGCTGAAGAAAGCAC[A/G]AAGCATCTCAGTCTA | 10580 |
rs74660575 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545349 | TTTCTTACCTCATCC[C/T]TGGCTTCTAGACTCT | 10580 |
rs74664489 | snp | C/T | 0.5 | 0 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351226 | CTGACCCAGATTTCC[C/T]TTTTGCAGTATCGTC | 10580 |
rs74699804 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324705 | CTGGATTAAGGTGTC[C/T]GTATCACAAAGGAAA | 10580 |
rs74743336 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397815 | GTTGGGCTTTTTTTT[A/T]AAGATAAAAATAAAA | 10580 |
rs74753186 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377404 | TAACTTTCTTAGTGA[C/T]CTTTACCATCCCTTT | 10580 |
rs74789302 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353518 | TCATTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 10580 |
rs74801997 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473627 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAATTG | 10580 |
rs74834958 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556264 | ATAAATCAATGGAAG[G/T]CCACACAGAAGTAAA | 10580 |
rs74837293 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491801 | TCCAAGAAAAAAAAA[A/T]TGGTAGAGCCCATAT | 10580 |
rs74854018 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524603 | TTTTATAGGAACAGC[C/G]ACGCCACTTGTCTCC | 10580 |
rs74903194 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327681 | TCTCCCTGGCCCCAA[A/G]TCCCCTCTAGAAACA | 10580 |
rs74909994 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430479 | GAAACAGAAAAAAAA[A/C]CAAATCCACACACGG | 10580 |
rs74910645 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353519 | CATTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCA | 10580 |
rs74912232 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537603 | TAGTTCTCAATTCTC[C/T]ATTAATCTGTATGAG | 10580 |
rs74914745 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439213 | CTTACTCATACCCCC[C/T]CTTCATGTAGGTGAT | 10580 |
rs74936427 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466441 | CAAGACTCCATCTCC[A/C]AAAAAAAAAAAAGAA | 10580 |
rs74965595 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370252 | ATATTCCTTTTGTAT[C/T]TTTTTTTTTTTTTTT | 10580 |
rs75022912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524926 | TTACTGGTGGAATGA[C/T]GCAGGGTTCAATTCT | 10580 |
rs75082114 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544970 | GTTCCTAGGGGGCCT[C/T]GCCCCCTCACACCTG | 10580 |
rs75153422 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312596 | TCTGTTTCTTGTTTC[A/G]TCATACATAGGAAGG | 10580 |
rs75154558 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314007 | ACCCTGGTTACTACC[A/G]TTTGTGTGATCCTTG | 10580 |
rs75158938 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340291 | CACCAACAAGATACC[A/C]TGTGTCATGCTGGGG | 10580 |
rs75166855 | snp | C/G | 0.084364 | 0.187256 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552482 | TCAAATACAGGAAAA[C/G]AGAGAAGATCCCAAA | 10580 |
rs75184514 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316210 | GCAATCTCAGCACTT[G/T]GGGAGGCTGAGGCAG | 10580 |
rs75185973 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378688 | CACTTCTAAAATGTA[C/T]ACTGTGTCTGTAATC | 10580 |
rs75187117 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326316 | GTGAACTATAGTACC[A/G]GAAGGGACATTGATG | 10580 |
rs75198602 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353241 | TAGGGCTTATATTAC[C/T]AAAATGGAATTTCAC | 10580 |
rs75203424 | snp | A/G | 0.0352966 | 0.128072 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314783 | TCAGATTACCCAAGA[A/G]GTGGAGGGGAGGGGA | 10580 |
rs75206250 | snp | C/T | 0.00436275 | 0.046501 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341439 | AGAGGTAAAAGAGAA[C/T]AAGGGAAGAGAAGAA | 10580 |
rs75279830 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525993 | AGGGCTGCAGGGAAA[C/G]ATGAGCACCATCACC | 10580 |
rs75332813 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374318 | CAACTAATTAGGGAA[A/G]AAATTCCACCATTTT | 10580 |
rs75342730 | in-del | -/CAACAGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470584 | ACTAAATCTGCAAGT[-/CAACAGT]TCATGCTTTCCTTGG | 10580 |
rs75360403 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398030 | CACAAGCTGTGCAAT[A/C]TTGGATGAGTAACAA | 10580 |
rs75375999 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480231 | GTTGCTGATGCTTAC[C/T]CTGCCCAAAGATAAA | 10580 |
rs75382343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461594 | TACAACCAAGTGACG[A/G]CAACACCAAGTATTA | 10580 |
rs75439630 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553255 | ATGTTATAAAACAAA[C/T]GTCTTAAGATGCTGT | 10580 |
rs75464320 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534629 | GATGTTAAGATCCTT[C/G]GGGTAGGCCTATTTA | 10580 |
rs75478100 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324071 | TTTCACAGAGAGACA[C/T]AGAAAAAGTGGGAGC | 10580 |
rs75485304 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404645 | GTAGCCTCAGAGCCC[C/T]GTGCAGTGCAGGGTA | 10580 |
rs75489036 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472441 | TGAATAAATCAAGGA[G/T]ACCGATGTAACCCAC | 10580 |
rs75489408 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455587 | GCTAGGTATCACTTC[A/C]TTTACATGTAAAACT | 10580 |
rs75506749 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549242 | TGACCGAGAAGCTGA[A/G]TTTTTAACGGTATTT | 10580 |
rs75519995 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490403 | ATAAGTATTTAAAAC[C/G]CATTATTTCCAACAT | 10580 |
rs75522289 | in-del | -/C | 0.365232 | 0.22186 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540255 | GGGTGGCAGCCGCAG[-/C]CGCGTTTTAGGTAAG | 10580 |
rs75549834 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482536 | AACAGAGCTACAGAA[C/T]TTCCTCTCAGTGCGG | 10580 |
rs75581414 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559807 | CCTCACAGCCCAAAC[A/T]CACGCCCCTCACTCT | 10580 |
rs75589680 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315558 | AGTTTCTAAAAGCCC[A/G]CTGACTATGGCCACC | 10580 |
rs75618826 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512695 | TCAAAAACAGAATCC[A/G]AGCCCTTTGACATGG | 10580 |
rs75632508 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505247 | GCAGGGCTGGGAAAC[A/G]GTGCCAGAAGCTCCT | 10580 |
rs75645449 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369027 | CCAGATTCTTTGCCA[C/T]ATACTCTAACTCCCA | 10580 |
rs75668896 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501389 | TTTTCCCAGCAAATG[C/G]CTGCTTTCCTGAGAT | 10580 |
rs75717896 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475213 | TGGTGGTGGGGGTGG[G/T]GGTGCAGAAGAGGGA | 10580 |
rs75747745 | snp | C/T | 0.0368353 | 0.130617 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312810 | GCACCCCTGAAAAAA[C/T]TATGAGATAAGATAG | 10580 |
rs75768655 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478746 | CACAGTTCCCTGGCA[C/T]CACACAGGAAAATTA | 10580 |
rs75786631 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331477 | CCTGACATAACTTCT[G/T]GTCCCAGCCCCTTCT | 10580 |
rs75786636 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467645 | TTCAAAGGCAGGTCT[C/T]GTGCAGAGGATTTGA | 10580 |
rs75808741 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335590 | GTTCCCAGGATCATA[A/T]GCCCTTGTAATCAAC | 10580 |
rs75813483 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539732 | GGGTGTTCAATAAAC[A/G]TTAGTGATTATTTAC | 10580 |
rs75816808 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313602 | CACCCTAGTTGTTTA[A/G]AAGTGAGCTAATGGA | 10580 |
rs75823303 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511263 | AGGCTGAAGTGCAGC[A/G]GTAAGATCATGATTT | 10580 |
rs75872300 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389419 | AGTTCTTTTTTTTTT[A/T]AAGAGACAGGGTTTC | 10580 |
rs75877540 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476007 | CACAAATATTGACTC[C/T]GCATCTACTGCGCTC | 10580 |
rs75879233 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494859 | TCAATTTTTATTTTT[A/G]TTTATTTATTTATTT | 10580 |
rs75911865 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526623 | AGTTTCCAGGTGATA[C/G]TGATGCTGGTGGTCC | 10580 |
rs75932867 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403093 | TCTCTGCAGAAGAAC[A/G]ATGGCCTCTCTACAC | 10580 |
rs75949477 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344422 | TGCTATTTTTTTTTT[A/T]AGATGGAGACTCACT | 10580 |
rs75962077 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410361 | TTTTTTTTGGTGTTA[C/T]GATTTGAAGAAGACA | 10580 |
rs75983820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542858 | TTCCCCTTCTACAAT[A/G]AAGAGAGGGGCCTCT | 10580 |
rs75984198 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385675 | TAAGGGACAGGCATC[A/G]GGTACCAAGGTACCT | 10580 |
rs75986638 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373330 | AGCCTAATGACTTAC[A/G]ATCATTTCTTTACTG | 10580 |
rs75999978 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370254 | ATTCCTTTTGTATCT[C/T]TTTTTTTTTTTTTTC | 10580 |
rs76000685 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404703 | GTGAACCCACAGAGC[A/G]CCGCCTGGTAACAGG | 10580 |
rs76014681 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389421 | TTCTTTTTTTTTTTA[A/G]GAGACAGGGTTTCAC | 10580 |
rs76040526 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358867 | TTTTTCAGCTCTGAA[G/T]ACCCATTGCTAGGTG | 10580 |
rs76051320 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499066 | TGAGTCTATAATGTT[G/T]TTTTTTTTTTTTTTT | 10580 |
rs76052175 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405664 | CCTGGACCCACCACC[A/C]CAGGGGCATCTACTG | 10580 |
rs76061055 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387982 | TTGCTACATCTTTTC[C/T]TTTTTTTTTTTTTTT | 10580 |
rs76068532 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386502 | TTAGCCAGGCGTGGT[A/G/T]GCATGTACCTGTAGT | 10580 |
rs76072080 | snp | C/T | 0.0138799 | 0.0821421 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311505 | AAGACATTTGTGCAT[C/T]ACTTTTGTTATCAGA | 10580 |
rs76075467 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494378 | TCCTGCCCACCAAAG[C/T]GCAGGACTCTACCGG | 10580 |
rs76091560 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391244 | CCTCATACTCCTCAT[C/T]GATAAAATGAAGAGT | 10580 |
rs76128422 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466811 | CTTTTTTTTTTTTTT[C/T]TCTAAGAAAAAATAA | 10580 |
rs76148565 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340292 | ACCAACAAGATACCA[G/T]GTGTCATGCTGGGGG | 10580 |
rs76182403 | snp | A/G | 0.290718 | 0.246662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484235 | TTCAACAAAAAAAAA[A/G]GTTGTTTTGTTGAAC | 10580 |
rs76186979 | snp | A/G/T | 0.0448719 | 0.142907 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434992 | TTGCCAAAGCTCTGG[A/G/T]CAAAGATTTACAGAG | 10580 |
rs76218603 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324587 | GAACTAAATGAGCCA[C/T]GTCATGCTTCTTCTA | 10580 |
rs76240678 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508319 | ACACTGATTAAATCT[A/C]CAGGAAACTGCTTCC | 10580 |
rs76247477 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476228 | AGAAATATTTTAAAT[C/G]TTGGGCTCTTGCTTT | 10580 |
rs76274225 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468218 | CATCTTCTAACAAAG[A/G]TGTTAGGCTAAAGAG | 10580 |
rs76283741 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437613 | CCCAGCACTTACTGA[A/G]TCCTGTGTGGCAGGA | 10580 |
rs76335403 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340290 | GCACCAACAAGATAC[C/G]ATGTGTCATGCTGGG | 10580 |
rs76366268 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314690 | GCCTTCAGGCTCAAT[A/G]ATTGAGATGGGAGCT | 10580 |
rs76374361 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424032 | GTGATTGGCATTCAC[A/G]TATAGCAGTGGTGTA | 10580 |
rs76443986 | in-del | -/C | 0.280785 | 0.248097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432113 | CGCACCGCTTACTTA[-/C]CCCCCATGCCCTAAG | 10580 |
rs76449364 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446377 | ATTAATTACTAAAAA[A/G]CCAAAGTTATACTCA | 10580 |
rs76472062 | snp | C/G | 0.000958313 | 0.0218687 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355829 | AACCACGGGCTTCCC[C/G]CCAGAAGGGGGCTGG | 10580 |
rs76473133 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498536 | TGAAATTTATCTGAA[C/T]AAAAGAAAGAAAGAA | 10580 |
rs76483296 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467227 | TGTTGTGAAAAAAAA[A/T]ATGTCTGACATTTAA | 10580 |
rs76487654 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502998 | ACACATACACACACA[A/C]ACACACACACACACA | 10580 |
rs76497752 | in-del | -/TTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377856 | GGCTTTTTTTTTTTT[-/TTT]CTTAAATAAAATGTA | 10580 |
rs76507420 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339455 | AAAACCTTCCCTGCT[A/G]AACCTGGAGGGAATT | 10580 |
rs76517529 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451808 | AAGGTAGGGCCATAG[C/T]CCACAATATAGGTAA | 10580 |
rs76526700 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467547 | AATAAAGGTTTACCC[C/T]AGTGACTTCCCACTA | 10580 |
rs76533136 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533038 | TCCCTTCGTAAGTCA[C/G]TCCCTCCCTATGGTA | 10580 |
rs76554480 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379382 | GAGACCCTATCTCAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs76570256 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451038 | CCTGAAAGAAAAAAT[A/T]CTAGGAGACAAGCTA | 10580 |
rs76578969 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500783 | CAAGAAGGCTGGCCA[C/T]GCTGGTTTCCACCTG | 10580 |
rs76582644 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510686 | AAGTTTTTGGAAAGT[G/T]AAGGTATTACCAGGC | 10580 |
rs76605383 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430175 | CTCAAATCCACACAC[A/G]GGGCCGGGCATGGTG | 10580 |
rs76613817 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499063 | CTGTGAGTCTATAAT[G/T]TTTTTTTTTTTTTTT | 10580 |
rs76635745 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514361 | CTGATGCTGGTTTAT[C/T]TCTGGCTAAAACCTC | 10580 |
rs76636220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502919 | TCCTCTCCTTTGGCC[C/T]CCATTCTCTCTTCTC | 10580 |
rs76641411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504763 | TTCTGGAAAAAGTGT[C/T]CAAAGCTTTCATCAG | 10580 |
rs76670660 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326492 | AAATGAAGGAAGAAG[A/G]CAAGATAAACATTTA | 10580 |
rs76677117 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485021 | TTCTGCTTCCTTTTT[A/G]AATTAAAAGGATTAG | 10580 |
rs76677138 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446821 | AAGGGAGCCAGCTCC[C/G]CACTTGAACAAAATG | 10580 |
rs76681704 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402168 | TCTCCTAAAGCTGCC[A/G]GTGTCCTTTTGATCT | 10580 |
rs76693392 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518165 | CAAAACCTAATGAGG[C/T]AGTTATGGTCCCCTT | 10580 |
rs76700761 | snp | A/G | 0.137867 | 0.223442 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429534 | ATACTTAATGAGCAC[A/G]TGGATTTTTTCTTTG | 10580 |
rs76705252 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407135 | CCAGAAGTAAACAGC[A/G]AGCAGCTCAGGAGCT | 10580 |
rs76794578 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524042 | AAGTTCGGGGTCTAA[C/G]AGTAGGAGACATGGG | 10580 |
rs76808755 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348715 | ACTACAGGACAGAGA[C/T]AACTGTATAAGAGGG | 10580 |
rs76811349 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389422 | TCTTTTTTTTTTTAA[G/T]AGACAGGGTTTCACT | 10580 |
rs76820882 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547801 | CCAATGGGGCACCCT[C/T]CCATCCCTGGGGCTA | 10580 |
rs76859196 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532056 | ATCAGAAATGAAGGG[G/T]GCAGCTTGGACACCT | 10580 |
rs76860127 | in-del | -/A | 0.161267 | 0.233723 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533588 | ACCAAAAGGGGAGTG[-/A]TGAGCTGTCAAACAA | 10580 |
rs76871924 | snp | A/C | 0.5 | 0 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414563 | CGGGGCAGGAGGGAC[A/C]AGCGGAGGTGGTGGT | 10580 |
rs76901577 | snp | A/G | 0.000115656 | 0.00760358 | missense | SORBS1 | GRCh38.p7 | 10:95432469 | TGCTTTCGTGTTGCC[A/G]GGTTTCCTGAGGGCT | 10580 |
rs76910879 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397941 | ACAGAGCTGATGAGA[A/T]GGTGAGTGGAAGGGC | 10580 |
rs76928312 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358865 | GATTTTTCAGCTCTG[A/T]AGACCCATTGCTAGG | 10580 |
rs76945139 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350283 | TTGGGTGTTATTCCC[C/T]CATTCCCCTAGCTCC | 10580 |
rs76959966 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345353 | CCTGACTCTAAAGCC[C/T]ACAATCTTTGCAGTA | 10580 |
rs76967331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518349 | GTATAAGTTTCTCTA[A/C]GAGTCTGTGAAGTAT | 10580 |
rs76976885 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396518 | ATTTTTTTTTTTTTT[G/T]GAGACAGAGTTTCAC | 10580 |
rs77034349 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319320 | TTGAAAGCTTTTTTC[C/T]TTTTTCTATCCCAGT | 10580 |
rs77037384 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316207 | CCTGCAATCTCAGCA[A/C]TTTGGGAGGCTGAGG | 10580 |
rs77060282 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344423 | GCTATTTTTTTTTTT[A/G]GATGGAGACTCACTC | 10580 |
rs77094890 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357224 | TAAAAAATTTCCAGT[C/T]GAGGTCCGGAAGCAA | 10580 |
rs77111758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464564 | GTCACTCAGGGTGCT[C/T]GCTGTCTAGCCCACT | 10580 |
rs77120932 | snp | G/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443179 | AACGTAGAAGCGGCC[G/T]GGTGTGGTGAGTCAC | 10580 |
rs77195353 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377264 | TGGGCTATAACACCT[A/G]AGGGAGGGGGTTGCC | 10580 |
rs77203737 | snp | A/C/T | 0.0174464 | 0.0919885 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514146 | AGGGGAAAAAATACA[A/C/T]CCTCGGGAGACACAG | 10580 |
rs77217428 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327683 | TCCCTGGCCCCAAAT[C/T]CCCTCTAGAAACAGC | 10580 |
rs77219663 | snp | A/T | 0.304188 | 0.244057 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544101 | GGAAACCACATGCGC[A/T]AAAGTCCTGAGGCTG | 10580 |
rs77234671 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317447 | GGCTGTTTGTTGAGA[G/T]AACGTCAATAAAAGC | 10580 |
rs77236415 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342727 | GGCATGTAGTCACCA[C/T]GCCTGGCCTAATTCC | 10580 |
rs77293147 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437870 | TCCCCTGTAGCCTAA[G/T]CCCCGCCCAGGTCCC | 10580 |
rs77341277 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523101 | GCTTTTGCACTTGAA[C/G]AGTTTAAAAGCAAGT | 10580 |
rs77350712 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504800 | AAAGGGGTCCATGTT[C/T]CAATAAAAACTAAGA | 10580 |
rs77352405 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318135 | GGTTTCAGGTTCAAC[A/G]TTAGCAACATCCACA | 10580 |
rs77352511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550307 | TCCTAGCACCGTGGC[C/T]TGCACACAGCAGGTG | 10580 |
rs77352883 | snp | A/G | 0.095934 | 0.196885 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316169 | TTCAAAGTGACCGAG[A/G]AGGCTGGGCATGGTG | 10580 |
rs77362992 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428414 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs77394408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459550 | GGAGCAGGCGGGCTC[C/T]GGAATGTGCCCTAGA | 10580 |
rs77415146 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365840 | TTTCTTCTTATGCTC[C/T]TGGGTATATTAATCA | 10580 |
rs77432688 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490342 | AAGGGAAAAAAAAAA[A/G]AGAGAATGGAAATCT | 10580 |
rs77445709 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435430 | AATGCCTGCCTGGGA[C/T]GTGGTGAAGGCTACC | 10580 |
rs77514391 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515777 | AGCCCAAGGGTGCTT[A/G]AGCTTGGATGGAGCT | 10580 |
rs77539654 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546161 | ACAGAAGAACAATTC[C/T]GGGATCTACTAAGCA | 10580 |
rs77540286 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358262 | ACTTCAAGTCCACTA[C/T]CTGGATTATTTTTCT | 10580 |
rs77581494 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351607 | CGGGATAGGGGAAGG[A/C]TGATTCCACATGATT | 10580 |
rs77598618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393331 | AAATGGCCTATGGTA[G/T]TTTAACTGTATCCAA | 10580 |
rs77599143 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95336054 | GCTCCCACACAAACA[C/T]GAGACAGGACAAAGA | 10580 |
rs77615761 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517421 | TTCAGCTCACTTGCC[A/G]CTTCTTTGGGAACCT | 10580 |
rs77623942 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397818 | GGGCTTTTTTTTTAA[G/T]ATAAAAATAAAACAA | 10580 |
rs77631452 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488827 | CGTATCATTCAATCA[G/T]CACTACTCTAATCCA | 10580 |
rs77654086 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353864 | ATAATTATCATCATC[C/T]TACTCATCCCCAAGT | 10580 |
rs77661745 | snp | C/T | 0.00957492 | 0.0685258 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377362 | CACAGTTAACATCCC[C/T]TTTGCAGCTTGTAGA | 10580 |
rs77683712 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435557 | AACTCTCCTCACACC[A/G]AGCCTGTTGTGAGGC | 10580 |
rs77706287 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387125 | GACTTTGTCTCTAAA[A/G]AAAAAAAAAACAAAA | 10580 |
rs77724618 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362637 | TCTTTGACACAGCTC[A/C]CATTAATCCCTTTAC | 10580 |
rs77727122 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464331 | CTTAAAAAAAAAAAA[A/G]GAAAAAAAAAAAAGG | 10580 |
rs77766192 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383421 | ACTCCGTCTCAAAAA[A/C]AAAAAAAAAAAACTC | 10580 |
rs77778444 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444386 | ATAGGTGTGAGCTAC[C/T]GCACCTGGCCTTTCC | 10580 |
rs77781097 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464607 | CATGTGACAGGTCCC[A/G]TATCATTTATTCTTC | 10580 |
rs77845631 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336071 | AGACAGGACAAAGAC[A/C]TGACAGAGCCGAGCA | 10580 |
rs77855870 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325727 | CAGCTTTTTTTTTTT[G/T]TACTTTTAGTAGAGA | 10580 |
rs77894611 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318222 | GAGAAGGCTCTTCTT[C/T]CTGTGCAGAGGAGAT | 10580 |
rs77903111 | in-del | -/C | 0.0524604 | 0.153226 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315972 | TAAAGCTTAGGAAAC[-/C]TAAAACATCTAGTTG | 10580 |
rs77906243 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316209 | TGCAATCTCAGCACT[A/T]TGGGAGGCTGAGGCA | 10580 |
rs77993720 | snp | A/G | 0.00616347 | 0.0551702 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356029 | CCAGGCGCCACTCAG[A/G]CTGTCTAGAGGTCTG | 10580 |
rs78002524 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557807 | CAATAGAGCCTCCCC[C/G]TTTCAAGCTCCATCC | 10580 |
rs78025648 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499080 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTAG | 10580 |
rs78042620 | in-del | -/CAAAAAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407945 | AGTGAGACCTTGTCT[-/CAAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 10580 |
rs78044720 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387134 | CTAAARAAAAAAAAA[-/A]ACAAAAAACACTTGT | 10580 |
rs78060718 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397940 | CACAGAGCTGATGAG[A/G]AGGTGAGTGGAAGGG | 10580 |
rs78085626 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405296 | AACTTTAAAAAAAAA[A/C]CTAGCTGGGCATGGT | 10580 |
rs78087037 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429222 | GCTGGAATGCAGTGG[C/T]ATGATCTCACTCACT | 10580 |
rs78091504 | snp | A/G | 0.141258 | 0.225111 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433456 | CACACAGTTCTGGGA[A/G]GCACACGCAGAGTGT | 10580 |
rs78100785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426115 | CTCATCTCATTCTAT[A/G]CTAATTTCATTTTGA | 10580 |
rs78112605 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422371 | GATGGCCTGATTACC[A/G]TAGGAACCCACTCGA | 10580 |
rs78140138 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334533 | ACCAAGAAAGGAACA[C/T]CAAGTTTCAACAAGC | 10580 |
rs78157743 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533249 | GTTCGCATAGGCCTG[A/C]CCACTGCAAAACATA | 10580 |
rs78163198 | snp | A/C/G | 0.0306829 | 0.12011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519824 | CTGCTCTCCTCTCCC[A/C/G]CTACTTACCAAGGCC | 10580 |
rs78167249 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407080 | ACTGTCATCATTCCC[C/T]TTGGCTGCGTTCCCA | 10580 |
rs78177165 | in-del | -/TC | 0.186737 | 0.241863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534954 | ACTGCACCATATCTG[-/TC]TCTGTCTCCCGTAGC | 10580 |
rs78190245 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480487 | GTGGTGTGGTGGAAA[A/G]AGCATGGCATTTGGA | 10580 |
rs78192784 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395150 | ACGAGTAGGAATCCA[C/T]ATACAATTTAGGCTC | 10580 |
rs78213952 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404287 | AGAGCCAAGTCCTGA[G/T]AAGGCTGAGAGGGTG | 10580 |
rs78216944 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387996 | CTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCA | 10580 |
rs78218473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494452 | CTCTTTCCAGATCTC[C/T]ACTTTGTGGTCATGT | 10580 |
rs78274608 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466812 | TTTTTTTTTTTTTTT[A/C/T]CTAAGAAAAAATAAT | 10580 |
rs78275307 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518283 | TAGAACCCAAATCAG[A/G]TCGCAAAGTGTGTGC | 10580 |
rs78276165 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501471 | ATCAGAAGGCAGCTG[A/G]TATTTTCTGCCCTCA | 10580 |
rs78401071 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363137 | CAATAGGTGCTCACT[C/T]CTCCCTCCTGGGCCC | 10580 |
rs78401678 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398411 | TTGGAGCCTGTTCCC[C/T]GGAATTCCTTAGGGC | 10580 |
rs78421209 | snp | A/G/T | 0.0641482 | 0.167434 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349606 | GCTATGACTATAGGC[A/G/T]TGTGCCACCAAGCCT | 10580 |
rs78434438 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554215 | CGCCACCGTGACTGG[C/T]TAATTTTTGTATTTT | 10580 |
rs78446430 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348879 | GGGATGTGTTGGTCT[C/G]TACTTTTTCTAGTCC | 10580 |
rs78448436 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557369 | TGAAAAGGGAGTATT[C/T]GAAACACTATCTCAT | 10580 |
rs78454166 | in-del | -/A/AA | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484226 | TTCAACAAAAAAAAA[-/A/AA]GGTTGTTTTGTTGAA | 10580 |
rs78465083 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468996 | ACACAGAGGAATCAA[A/G]TCCTTCGTCATTGCC | 10580 |
rs78472920 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371858 | AACCAAAAAAAAAAA[A/G]GCATCAAGTTTTTTC | 10580 |
rs78481004 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364440 | TAAATTGTGTGTGTG[-/T]GGGGGGGGGTGTTTG | 10580 |
rs78492280 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382113 | CTTTCACCTTGCTTC[A/G]CTCTATGGGCTTTTC | 10580 |
rs78496625 | snp | C/G | 0.021333 | 0.101051 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333048 | GAGCCAGCAAAAAGA[C/G]GTAGCTCTGCAAAGC | 10580 |
rs78545030 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317102 | TGACTTCTCATTCAT[A/G]TTGAGGTCTTGCTGT | 10580 |
rs78570465 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479058 | TCCCTGAATGGAAAC[G/T]CCTGGTTGGAACTCC | 10580 |
rs78579544 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528433 | CCTTGTCCAAAATCC[A/T]TTTCACTCACACCTG | 10580 |
rs78595275 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330022 | CTCAGGCCTTGGTTT[C/T]CTCATCTCATTGTAA | 10580 |
rs78595902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493504 | TCTGCCCATCAAAAT[C/T]CCCACATGGAGTTCT | 10580 |
rs78606490 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430480 | AAACAGAAAAAAAAA[A/C]AAATCCACACACGGT | 10580 |
rs78612243 | in-del | -/AAA | | | utr-variant-3-prime, cds-indel | SORBS1 | GRCh38.p7 | 10:95312978 | ACAACAAAAAAAAAA[-/AAA]CAGTGCTCTTAGATG | 10580 |
rs78623066 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487008 | TCCTGAAATCACTTA[A/C]TGAAGGAGGAATCAG | 10580 |
rs78635223 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433503 | GAGCTATGCAGAACG[A/C]CACAGTTTTGTTTTG | 10580 |
rs78668226 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339770 | AATCATCACCCATCA[C/G]ATAGTCATTTGGGGA | 10580 |
rs78668493 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498895 | TGTGCACACACACAA[A/C]TGAGTACATATAACA | 10580 |
rs78683409 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466798 | ATATCGCAGATTTCT[C/T]TTTTTTTTTTTTTTC | 10580 |
rs78686393 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549144 | GAGTTCCTCCTGAGA[C/T]TACAGAAACACTCTA | 10580 |
rs78761243 | snp | C/T | 0.00365007 | 0.0425642 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356516 | CTTGGGGATGTGTTC[C/T]GAGCCCTCCTGGCTG | 10580 |
rs78761667 | snp | C/G | 0.030665 | 0.119967 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539561 | GTTGGAGTCCTGGCT[C/G]TACATTGTACTAATT | 10580 |
rs78796746 | snp | A/G | 0.247053 | 0.249983 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498590 | GAAAATTGGAGGTCA[A/G]CGGGCCACACCAGGC | 10580 |
rs78830738 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343609 | TTTTCTTGAATTAAA[-/AAA]TAATTTTAAAATTGT | 10580 |
rs78836691 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554049 | TTCTAGTAGTATTGA[C/T]TTTTTTTTTTTTTTT | 10580 |
rs78838677 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518234 | ACATACTCATGATCA[C/G]ATAGTGAATAAGTAG | 10580 |
rs78854451 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358866 | ATTTTTCAGCTCTGA[A/G]GACCCATTGCTAGGT | 10580 |
rs78863072 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490332 | TAGTGGTAGGAAGGG[A/G]AAAAAAAAAGAGAGA | 10580 |
rs78863429 | in-del | -/CCGC | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442524 | TGTGGCACCCCCCCC[-/CCGC]ACCCTTACTTATGCT | 10580 |
rs78867740 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534958 | GCACCATATCTGTCT[C/G]TCTCCCGTAGCAAGA | 10580 |
rs78875224 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353301 | ATACATGGGAATCTT[A/G]TATCTTGTGGCAGGA | 10580 |
rs78880482 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352157 | ACCCTAAGAATAACG[C/T]TACCTGGGATTAGAA | 10580 |
rs78918639 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333766 | GTGAGACCCTGTCTC[A/C]AAAAAAAAAAAAGAA | 10580 |
rs78981593 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413875 | ACCTTCTCCTCAGGG[A/G]CCCTAGCAATTGCCT | 10580 |
rs78981710 | snp | C/G/T | 0.00210805 | 0.0323977 | missense | SORBS1 | GRCh38.p7 | 10:95341385 | GTCAACTTTTTGGGC[C/G/T]GTGCCTTCTCAGCAG | 10580 |
rs78985651 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539073 | CACCTTGGCCCATCA[A/G]GTCTCAGTCAGTGAC | 10580 |
rs79003246 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395424 | AACATGCTATCCTAA[C/T]ATGATTTTTTTAAAT | 10580 |
rs79016977 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526343 | AGATCACCTGGGCAG[A/C]CTCTGCACAGGCCCC | 10580 |
rs79024277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457451 | CAGCACTAACCTCCC[A/T]GTTGTGAGGATTAAT | 10580 |
rs79030858 | snp | A/G | 0.267364 | 0.249396 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403748 | TGTATTTTTAGTAGA[A/G]ACGGGTTTTCACCAT | 10580 |
rs79040099 | snp | C/G/T | 0.351853 | 0.228311 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364442 | AATTGTGTGTGTGTG[C/G/T]GGGGGGGTGTTTGCT | 10580 |
rs79049119 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380018 | CCTTGGCCTGCCTTT[C/G]GTGTTCATGCCCCAT | 10580 |
rs79051119 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453840 | GCCCGCTGCAGGACA[C/T]AAGTCTGCTCAGATT | 10580 |
rs79056247 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406526 | AATGTAATTATAATC[A/G]CAACCATGACAGTGA | 10580 |
rs79063241 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379389 | TATCTCAACAAAAAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs79067511 | snp | A/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409243 | TCTGTTTGACTGAAT[A/T]TTTTTTTTTTTAAAT | 10580 |
rs79069169 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535401 | ACAGCAATTAAACTG[A/C]TAAACCAAGGGAAAG | 10580 |
rs79072198 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316482 | GCAAGTGAAGAGTTC[A/G]GGGATGCAAGGAAGA | 10580 |
rs79075027 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342286 | AGTAGCTCTGGGACC[C/T]TGGACACAATACTTA | 10580 |
rs79093207 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318932 | AGGGTTCACGCTCCT[C/G]TGAGAATCTAATGCA | 10580 |
rs79098607 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389578 | AGTTCTAAAGAATGC[A/C]AAAAAAAAGACCAGG | 10580 |
rs79115442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482707 | CCACAGAAGTTGTTA[C/T]ATGGCCAGTACTCCA | 10580 |
rs79120184 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475239 | AGGGAGATACCCTAG[A/T]CACTTGTCTTCAGAT | 10580 |
rs79120658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372972 | AATAGCTCCTAAAAT[G/T]TTGTGCAAATTTCAT | 10580 |
rs79125602 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447775 | ATACTTCCGTTCAAG[A/G]GGAAGAAAGTGGGAT | 10580 |
rs79128059 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419059 | AGAGCAAGACTGTCA[A/C]AAAAAAAAAAAAAGT | 10580 |
rs79167614 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493582 | GGCTGAGGCAAAGCC[A/G]GGGAAAAGCACTCCA | 10580 |
rs79224692 | snp | A/G | 0.100588 | 0.200439 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488284 | ATTTTCTTGATTTGG[A/G]GAAGTCACAGCACTT | 10580 |
rs79253064 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345368 | CACAATCTTTGCAGT[A/G]TATTACACAGCCACC | 10580 |
rs79302836 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327825 | CCCTGACCTCCCAGC[A/G]GGACAGTGAGAAAAT | 10580 |
rs79341006 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342400 | TAGGATGGTGCCTGT[G/T]GTACAGGTAGGTAAC | 10580 |
rs79354318 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316211 | CAATCTCAGCACTTT[C/G]GGAGGCTGAGGCAGG | 10580 |
rs79359100 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543118 | CTTACTAAAGTATGT[A/G]CCCTTCTCCCAATCC | 10580 |
rs79391075 | snp | C/T | 0.0603597 | 0.1629 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314165 | CTATGAGAATAGGCC[C/T]CCCAATTCTAAACTG | 10580 |
rs79403030 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384730 | TCTTACCGGGGCCTC[A/G]GGCTGCTATTGGGTG | 10580 |
rs79435956 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535424 | AGGGAAAGGCAACTA[A/T]CTATCAGTCTCTACA | 10580 |
rs79509071 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553881 | CTAACTGCCATGCCT[A/G]GCTAATTCTTTGTAT | 10580 |
rs79522693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540804 | CACTAGCCATCAGTT[C/T]CCTACCTTGAGAATT | 10580 |
rs79527204 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379405 | AAAAAAAAAAAAAAA[A/C]GACCTTCATATGAGT | 10580 |
rs79540778 | in-del | -/AAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392280 | AAAAAAAAAAAAAAA[-/AAAA]CCTCAAAACCAAAAA | 10580 |
rs79546527 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552401 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 10580 |
rs79576873 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458733 | TCATTCATTCAGTAA[A/G]AGTTCACTAAATGTG | 10580 |
rs79600974 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526398 | GAGGGGAGTTGGGGG[G/T]AACAGATATAGTTTT | 10580 |
rs79603319 | snp | G/T | 0.131038 | 0.219882 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442737 | ATGGCCTAATACAGT[G/T]AGTCTTCCAACTTGA | 10580 |
rs79613543 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482177 | CACAGCAAAACACCC[C/G]CTGCAGCCTCCATTA | 10580 |
rs79614095 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448822 | ATTTTCCAATGTTCA[A/G]TGACATACCTTCTAA | 10580 |
rs79617758 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340293 | CCAACAAGATACCAT[G/T]TGTCATGCTGGGGGC | 10580 |
rs79622952 | snp | A/T | 0.21845 | 0.248001 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523559 | GTTCCCTGCAGTTTT[A/T]AAAAAATACATTTAG | 10580 |
rs79647412 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507463 | TTAATAAAATGTATA[A/C]GTAATTTAATCTTCA | 10580 |
rs79647676 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326310 | TTAATTGTGAACTAT[A/G]GTACCGGAAGGGACA | 10580 |
rs79657549 | snp | A/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442230 | GCAACTGGTTAGATA[A/T]GGCTGGGTCAATTTC | 10580 |
rs79697574 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467226 | ATGTTGTGAAAAAAA[A/T]TATGTCTGACATTTA | 10580 |
rs79729192 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332169 | TTGCCTTCTTCAAAT[A/C]TATACTGTTATCAGT | 10580 |
rs79750362 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548239 | GCAGCCCCTGGCTGA[A/G]AAACATTCCATTACG | 10580 |
rs79752019 | snp | A/T | 0.0652144 | 0.168387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555495 | TAAACACATTTTCGT[A/T]GAACGTCAATTGTAT | 10580 |
rs79753644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501904 | TGCCCTTCTAGGAGC[C/T]GACAGGAAGAAGCTC | 10580 |
rs79760979 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425934 | AGAGCTCCCAAGCTG[G/T]GGGGAGTGCCTCGGA | 10580 |
rs79814428 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539200 | TGCTCTGAGTGGTAA[C/T]GATACAACCAGGATC | 10580 |
rs79815061 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464343 | AAAAGAAAAAAAAAA[-/AA]GGCTCAAATTCAGGT | 10580 |
rs79815067 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468220 | TCTTCTAACAAAGGT[A/G]TTAGGCTAAAGAGAC | 10580 |
rs79826804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533864 | TTCCTGGCCTGGCTA[C/T]CTCTTATCCTGGACA | 10580 |
rs79850923 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424586 | AAATATACAGGAGAT[C/T]TGCATAGGTTATGTA | 10580 |
rs79869067 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381423 | CAATCTTTATGTTAG[C/T]AGAAAAATTAATATT | 10580 |
rs79909826 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482332 | GCTTTGGACCCACCA[A/C]AAAAAAAAATTAAGA | 10580 |
rs79940339 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506595 | AATAAATCAAAATCA[C/T]AGTAAGAAAAACAAA | 10580 |
rs79945208 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342079 | CACTATCCTCTTCTA[C/T]GCCCTAGCAGGGCAT | 10580 |
rs79958598 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468964 | AATGACAATGTGATA[C/T]GTGTAAAACCTTAGG | 10580 |
rs80011041 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377857 | GCTTTTTTTTTTTTT[C/T]TCTTAAATAAAATGT | 10580 |
rs80014339 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499075 | AATGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10580 |
rs80034760 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425011 | CAGGCCCTTAAACAC[C/G]TGGTGACATGCCATG | 10580 |
rs80035250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544670 | GCATCTTACAACGTC[C/T]TCATGACATCCTTGC | 10580 |
rs80059119 | snp | A/C | 0.00266311 | 0.0363932 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356384 | TGAGGTCAGGCTGCC[A/C]CGGGACAGCACAGGT | 10580 |
rs80089679 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506563 | CTCATGTCACTGATA[C/T]CATTCTATCAGACTC | 10580 |
rs80096618 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512951 | TTCGGGGGTCAGGGC[A/G]AAGTAGTGGACCAGT | 10580 |
rs80111319 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434329 | AGGATGTCCATGCAC[C/T]GCAGACCCATCCCAA | 10580 |
rs80124322 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413106 | TGCAGGCATACATCT[C/T]TACACAAAGGGATGT | 10580 |
rs80180278 | in-del | -/CAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383415 | AGCAAAACTCCGTCT[-/CAAAA]AAAAAAAAAAAAAAC | 10580 |
rs80191773 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379386 | CCCTATCTCAACAAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs80222401 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396519 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTTTCACT | 10580 |
rs80235691 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358868 | TTTTCAGCTCTGAAG[A/T]CCCATTGCTAGGTGG | 10580 |
rs80246562 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455645 | GGATATACAGAACCC[A/G]TCTTCCACATTGCGT | 10580 |
rs80260769 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473033 | AAGATTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 10580 |
rs80261260 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524655 | GTGCCACAATGGCAG[A/G]GTTGAATAGTTACAA | 10580 |
rs80267801 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445068 | ATGCTGAGAGGGTAG[A/G]AGGAGAATGGACCCT | 10580 |
rs80279163 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481654 | TGCAGGCTGTTGCCC[A/G]TGCATGTGACTGGGC | 10580 |
rs80283246 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412421 | TCCACAGAGGCTCCT[C/T]CTCTTGACAGAGGAG | 10580 |
rs80289743 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533227 | CATCCTTGAACTTTG[G/T]GGGTAGGTTCGCATA | 10580 |
rs80311247 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500095 | GGGTGTGCGTTCCCC[A/C]ACCTTTCTTACCACC | 10580 |
rs80314192 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534954 | CACTGCACCATATCT[C/G]TCTGTCTCCCGTAGC | 10580 |
rs80327003 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324264 | GGACAGGGTTTATCA[C/T]TGTTTTCTTAAAAAA | 10580 |
rs80347446 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533485 | GGCACACAGACAACA[C/T]TATGCCACAGTCCAA | 10580 |
rs111225995 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390970 | TATATTTCCAGGCAC[A/C]ATCTGGGAGGTACTG | 10580 |
rs111227571 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400162 | TATGTGCCAAGCAAT[A/G]CAATAAACTCTTCAT | 10580 |
rs111233507 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383799 | TAACCTTGCACTATC[C/T]TTACTAGGAATCATG | 10580 |
rs111261988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327900 | CAAAATGCTTAACGT[C/T]TTAGGACTTCAAGTT | 10580 |
rs111269139 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495599 | TGTTACTGCTGTTGT[G/T]TTAAAATTTTAAGGG | 10580 |
rs111283534 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364441 | AAATTGTGTGTGTGT[G/T]GGGGGGGGTGTTTGC | 10580 |
rs111309134 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559962 | ATCACCACCAAGATA[C/T]CTTTCCAACCAAAAC | 10580 |
rs111333176 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405531 | ATCCAAATCTCTAGG[A/G]GGATGGCCTAGGAAT | 10580 |
rs111342416 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322321 | ATATTCCAGTAGTGG[A/G]GTGCAGGAGGGATCC | 10580 |
rs111355246 | in-del | -/TC | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325558 | GGCACTACTTCTTTT[-/TC]TTTTTCTTTTTTTTT | 10580 |
rs111362427 | in-del | -/A | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462820 | TATTTATTGCTAGGG[-/A]AAAAAAAACCCTATT | 10580 |
rs111380750 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470710 | CTCTATGTCCTGCTG[C/T]ATTCCCAAACAACAA | 10580 |
rs111385662 | snp | C/T | 0.185155 | 0.241444 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341064 | CAGGCTAGTCTCAAA[C/T]GCCTGACCTCAAGTG | 10580 |
rs111387169 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349039 | ACCCAGGGTCTGTAT[G/T]TTACCAAGCCCTCCA | 10580 |
rs111414059 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527383 | GTGAGCCGAGATCAC[A/G]CCACTGCACCCCAGC | 10580 |
rs111428126 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545836 | TATAAGCAATTACAA[A/C]CCCTGGCCATAATTC | 10580 |
rs111428879 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554943 | CTGGAGTGCAATGGC[G/T]TGATCTCGGCTCACT | 10580 |
rs111436203 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401502 | TGCTCAGTTAAAACC[C/T]GCTTATTGATTGACT | 10580 |
rs111439990 | in-del | -/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477870 | GCTAAAACAAAACAA[-/C]ACACACACACACACA | 10580 |
rs111440220 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453415 | CGATCTTGGCTCACT[A/G]CAACCTCCGCCTCCC | 10580 |
rs111442407 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394884 | GAAATAAAATTTTCA[C/T]CAGCCAAAAATGACT | 10580 |
rs111455423 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428676 | GTGGGTATCAGGGGA[C/G]CAGGTAGGGACTGGA | 10580 |
rs111485279 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364594 | AGCTGGGACTACAGA[C/T]GTGCACCACCAAGCC | 10580 |
rs111486439 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505323 | ACGTGGATGCTGGAG[C/T]TGGGGGATTTGGCTC | 10580 |
rs111502617 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547605 | GGGTGTGGTGGCGGG[A/C]ACCTATAAGCCCAAC | 10580 |
rs111515172 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452350 | TAAGCCCTGAGCACA[A/G]GCTCTGAGGCCATGG | 10580 |
rs111534538 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399985 | GCCTTCAGGGAGCTT[A/G]CAGTCTAGTGGGCAG | 10580 |
rs111536045 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354839 | TACTTGCTTCATACA[C/T]TTTTCCAAGCAAAAA | 10580 |
rs111538067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371543 | GTTATACTTTCATAC[A/G]GCCAAGATAGCATGA | 10580 |
rs111550282 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334280 | GCCCAAGACACAGGA[A/G]CCCCTTCTGAAGGAC | 10580 |
rs111579024 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412917 | CCTGGTGCTGACCTA[A/G]CTACACTGCACAGCA | 10580 |
rs111582804 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347542 | CAGGTTCAAGCAATT[A/C]TCCTGCTTTAGCCTC | 10580 |
rs111590188 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366702 | TTTTTTTTTTTTTTT[C/T]AGATGGAGTCTCACT | 10580 |
rs111601104 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405921 | TGGCTCACTGGTCTG[A/G]TCTGTCCACCACCCT | 10580 |
rs111606185 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320599 | TGGCCAGGACAGTCT[C/T]GATCTCTTGTCCTCG | 10580 |
rs111624074 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452962 | TTAATTTGTCAGCCT[C/T]GGTTTACTCATCCAT | 10580 |
rs111634027 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408867 | GAACATATGGTTTTG[C/T]TCTTTATGGAAATCT | 10580 |
rs111663161 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506081 | TCTCTCTGTCTCTTT[C/T]TCTTGGTTTAAAGCA | 10580 |
rs111681336 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404471 | GTGCAAATCCACAGA[A/C]ATCATGTGCACATGT | 10580 |
rs111698351 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337693 | CATCCAGATCCCTGA[C/G]CCGGAACCATACGGG | 10580 |
rs111703437 | snp | A/G | | | utr-variant-5-prime | SORBS1 | GRCh38.p7 | 10:95561365 | GCGTCCGCCCCACTC[A/G]CACTACACGCTGCAG | 10580 |
rs111733746 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463875 | AAGGTGAGAGAACCA[C/T]CAGGAAATGGGTCCA | 10580 |
rs111735153 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454281 | TGTATGCATTCTGTG[C/T]AAGGCCCTGTGCTCA | 10580 |
rs111740404 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354597 | TCTAGCTTACAGGGC[A/C]TTAAGTGCAGCAGTG | 10580 |
rs111755519 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325478 | CATTACATATCTGAC[-/T]TTTGTACTAACCCTC | 10580 |
rs111759814 | in-del | -/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450506 | CATTTGTGATTACAA[-/C]TTTTTTTTTTTTTTG | 10580 |
rs111770144 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438864 | TTGCTGTCCAGCTTC[A/C]TGAGTTTGATTCAGC | 10580 |
rs111772347 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439418 | CCCCTCCCTTCCTCC[C/T]TCTCTGGCCCTTGAT | 10580 |
rs111793745 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495943 | GTTTTTGTTTTTTTT[G/T]AAACAGAGTCTCACT | 10580 |
rs111799606 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419319 | AAAGCTTTCAGGTGA[A/T]CTCACTTGGTTTCAG | 10580 |
rs111816625 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351078 | AAGAAGCCAAAGCAA[A/G]CCTAAGGGAGGCCAG | 10580 |
rs111826842 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354610 | GCATTAAGTGCAGCA[G/T]TGGACAATCTCTGTA | 10580 |
rs111827693 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425295 | AAACAGCTATGTCAC[A/G]GAAAGCTGAAATGTG | 10580 |
rs111830243 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383651 | TGACAAATCTTGCAG[C/T]TAAGATTTCTCTTGT | 10580 |
rs111856689 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536872 | CACATTGGGACGAAG[C/T]ACCCTGGGAAACTGG | 10580 |
rs111857940 | snp | C/T | 0.000246236 | 0.0110931 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337164 | GTCAGGGCCAGAGAA[C/T]GCCTGCCTGGGACCC | 10580 |
rs111881139 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416438 | AGAGAGGCTGAGCCC[A/T]GCCCGTAGCAGGCCA | 10580 |
rs111898672 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558030 | ACCGTGGCTCAAGCC[C/T]ATAACCCCAGCATGC | 10580 |
rs111923958 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427385 | AGACCTGGTGTGGCA[A/G]TGAGGTCAGGAGGCA | 10580 |
rs111930843 | snp | C/T | 0.323671 | 0.238899 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552376 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 10580 |
rs111932221 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386362 | AAATACTGGTTGAGC[A/G]TGGTGGCACATGCCT | 10580 |
rs111938997 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546543 | AATGACCAGGTCTCA[C/G]AAGAACTCACTCACT | 10580 |
rs111952235 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538798 | TGCAATGAGCTGTGA[C/T]TGTGCCACTGAACTC | 10580 |
rs111956160 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364731 | TGTTGGGATTACAGA[C/T]GTGAGCCACCACGCC | 10580 |
rs111961046 | snp | A/G | 3.29897e-05 | 0.00406125 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321954 | TCGAAGTTCACCAGG[A/G]GTACTTACAAATCTT | 10580 |
rs111966535 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487256 | GTACCACTCAGAGTG[C/T]TTTCACTCAAGCTGG | 10580 |
rs111979290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406668 | GTACAGAGGAGGAAA[C/T]GAAAGCCTGGCCTTA | 10580 |
rs111985876 | snp | A/T | 1.67761e-05 | 0.00289617 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432616 | AAGACTGAATCCAAG[A/T]CTCCTGAAGGATTAA | 10580 |
rs111993591 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516471 | ATACCCTCTTCTAAT[C/T]CTAAGGCTCTGTAGT | 10580 |
rs111994856 | in-del | -/G/TG | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367225 | TCCTTTTTTTTTTTT[-/G/TG]GGGTAGAGACAGGGT | 10580 |
rs112001037 | in-del | -/GAA | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415115 | TTTATGAGAGAGAAA[-/GAA]GAACAGAACAGGCAG | 10580 |
rs112002550 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360106 | AATTAAAAATAAATA[C/T]GTCCCTTTTCTAAAT | 10580 |
rs112006248 | snp | A/G | 0.000601938 | 0.017338 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356177 | TCTGCTGTCAGTGGA[A/G]ATATTTGAACAGCGG | 10580 |
rs112017288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380319 | AGAAATTAAGAAAAG[A/G]GAGCCTTCGGTAAGA | 10580 |
rs112019247 | snp | A/G | 9.55466e-05 | 0.00691116 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414423 | GCTCAGTGCTTCAGT[A/G]AGAAAGGGAATGTGA | 10580 |
rs112021613 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324061 | GACCCACTTGTTTCA[C/G]AGAGAGACATAGAAA | 10580 |
rs112044835 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313070 | GAAGTCTCCTTCTAC[C/T]CAGAAAGCTCACCCC | 10580 |
rs112047904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324485 | CCTGTCCTTTTGGGA[A/G]GCCTCCTCAAGTTCT | 10580 |
rs112066392 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492893 | TCTTGACAAGTGTCC[A/G]TATCAAAAATGTCAC | 10580 |
rs112071928 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322476 | TTAGGGTAGAAATGC[A/G]AGTATGTATCCCCAA | 10580 |
rs112077550 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392614 | GCTTCTAAATTATAT[G/T]TGATAAGTTATCATG | 10580 |
rs112119397 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496626 | ATTAGTTGAAAATAA[C/T]AAAATGAGTTTAGCT | 10580 |
rs112137556 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433007 | CCAGGCTGGCAACTA[C/T]GGAAGTGGGGGCGGT | 10580 |
rs112145042 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519493 | TCTGCAAAACCCATA[C/T]TGACTTTTACATGTA | 10580 |
rs112171702 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375445 | CTACATCATAGAAAT[A/C]ATTCCCTAAAAGTCA | 10580 |
rs112201449 | snp | A/G/T | 0.00875054 | 0.0656008 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546251 | GCCCAAACAAGAATG[A/G/T]ATTGGCAAAGCCAGT | 10580 |
rs112229041 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401804 | CATCATCACCATCAA[C/T]GTCAAAGGATGTTAA | 10580 |
rs112233636 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346283 | AACTCTATGAACTAC[C/T]GTTTTGTTCTTTTTT | 10580 |
rs112242704 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526440 | CCTCTCTCAGGCGCA[A/T]CCAATGTGCAGGCAA | 10580 |
rs112256164 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317947 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAAGTTG | 10580 |
rs112283854 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396595 | CAACCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 10580 |
rs112286574 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498758 | GCTCCTAGGCTCAAG[A/C]GATCCTCCTGCCTCA | 10580 |
rs112334750 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371554 | ATACGGCCAAGATAG[C/T]ATGATTAAAACACAA | 10580 |
rs112338628 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525648 | CAGTACTTAAAAAGC[C/T]GCCTCATTTCTTTCT | 10580 |
rs112372646 | snp | C/T | 0.0650779 | 0.168237 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397301 | GTAGAAAAACAAAGG[C/T]AAAGAGCAAAATTAA | 10580 |
rs112376327 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530744 | TTAGCCAGAGCTTCC[C/T]GAGTCTCAGACCTTC | 10580 |
rs112405951 | snp | C/G | | | splice-acceptor-variant | SORBS1 | GRCh38.p7 | 10:95410778 | TAGAGGACTGGAATC[C/G]TGAAACGAACAAACA | 10580 |
rs112410516 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345963 | TCTCTTGGGATGTTG[C/T]AGCAAAATGGGTAAA | 10580 |
rs112411091 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395240 | TAAAAATCCAGTCCT[C/T]TTGCCTGAATTACCG | 10580 |
rs112418279 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528097 | ACTGTGGGCAGAACA[C/T]TATGCAAGACCCTTG | 10580 |
rs112423130 | snp | C/T | 0.089084 | 0.191327 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403794 | CTCCATCTCTTGACG[C/T]TGTGATCCACCTGCC | 10580 |
rs112431039 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409256 | ATTTTTTTTTTTTTA[A/T]ATATGAGTCACAAGG | 10580 |
rs112469964 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551703 | AGAAAACCATAAAAA[A/C]AACAAAAACAAACAA | 10580 |
rs112502416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359392 | AGCTCCTGTTTTATT[C/T]TACTGCTCATTAATT | 10580 |
rs112506808 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465612 | CTTGCCAAATATAGA[A/G]TTAATGGAATGTTCT | 10580 |
rs112510020 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415111 | AACACTTTATGAGAG[A/G]GAAAGAACAGAACAG | 10580 |
rs112520098 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451805 | ATCAAGGTAGGGCCA[C/T]AGTCCACAATATAGG | 10580 |
rs112520591 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335293 | TTCTCAAGAGGAGAG[A/G]CAAATGACCTTTGTA | 10580 |
rs112520840 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549363 | CCATTTCTCTTTGTT[C/T]GCTGCTATATTCCCA | 10580 |
rs112522304 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320206 | AGAGCTCTCACTCTG[C/T]CCCCACTTCTGGAGA | 10580 |
rs112550039 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488398 | GAAACCATATTCATT[A/G]GCATGTCTTTATTTA | 10580 |
rs112560843 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394097 | GAAATGTCATCTCCC[A/G]CTATGACTGAATCTT | 10580 |
rs112561400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421837 | GCTTATCCAGAGTTG[C/T]CCAAAAGCTTGAAAC | 10580 |
rs112563646 | snp | A/C | 0.00677167 | 0.0578647 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460182 | AAAGAAACACCAATT[A/C]GTTACAAGAATCATT | 10580 |
rs112570028 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312637 | CAAATTTTAACACAA[G/T]ATTTTATTAAAGACG | 10580 |
rs112583068 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369472 | ACACCCAACCAACAC[C/T]TCAAAGGTCAATTAC | 10580 |
rs112607171 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484901 | ACTGTTTGAGCCTGG[A/G]AGGTCGAGGCTGCAA | 10580 |
rs112643709 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317694 | AAAAATAAAATTTCC[A/G]AATGCAAAATAGACA | 10580 |
rs112644578 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520902 | TAGTTGGCAGTTAAA[C/T]TGAAACCAACAGACT | 10580 |
rs112654709 | in-del | -/GTAA | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406170 | AAAAGAACACACAGT[-/GTAA]GTAAGATTTATACAG | 10580 |
rs112657310 | in-del | -/T | 0.461813 | 0.132798 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521429 | CTTTCTCTCTTAGCA[-/T]TTTTTTTTTAATGGA | 10580 |
rs112658190 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453029 | GGTGGCTCACACCTA[A/T]AATCCCAGCACTATG | 10580 |
rs112669418 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374144 | TGTTCTCAACATTTG[C/T]TTGAAGTTAGCTGTG | 10580 |
rs112694345 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344137 | CTACTATTAAGCAAA[A/G]GACCCACTTGTGTGT | 10580 |
rs112700240 | snp | C/T | 0.5 | 0 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311482 | ATAATGTTTTACTTT[C/T]GTTTTTAAAGACATT | 10580 |
rs112704057 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462836 | AAAAAAAACCCTATT[A/G]TTATCATCAAGAGCC | 10580 |
rs112723489 | in-del | -/A | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473030 | GAAAGATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10580 |
rs112736191 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558637 | TCTCCCACAACCACT[A/C]ACTCTGGGGTCTGTG | 10580 |
rs112757712 | snp | C/G | | | splice-donor-variant | SORBS1 | GRCh38.p7 | 10:95341563 | AAAGAGGCTGCGGTA[C/G]CTCGATGTAGGTGCG | 10580 |
rs112761678 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436508 | GGACATACCCTCTAC[A/G]GCTGGTTCCTTTCAC | 10580 |
rs112769892 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425702 | AGTTCTCAGGACCTC[G/T]TAAATGTTCCTCTCT | 10580 |
rs112774890 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346253 | AGTACTCTGAATAGT[G/T]TTTGGCACATAGCAA | 10580 |
rs112778180 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400761 | GATGCAAAGTAATCC[A/G]AGGGACAGGAGATGA | 10580 |
rs112802115 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488549 | GGCTTTAAATATCAT[C/T]TACATGCCAATGACT | 10580 |
rs112814142 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490419 | CATTATTTCCAACAT[A/G]TCAGTTTCACACTTT | 10580 |
rs112816343 | in-del | -/CTGGGATTACAGGCCTTAATGCAATT | 0.347032 | 0.230401 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340828 | TGGTTTCCCAAAGTG[-/CTGGGATTACAGGCCTTAATGCAATT]CTTTTTTTTTTTTTT | 10580 |
rs112845001 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484843 | AGCTGGGCATGGTGG[C/T]GCACACCTGCAGTCC | 10580 |
rs112849311 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317740 | TATAAGTGGAGACTA[G/T]GGCCGGGTGCGGTGG | 10580 |
rs112878216 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552954 | GCACGGTGGCTCATG[A/C]CTGTAATCCTAGCAC | 10580 |
rs112880152 | snp | G/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538220 | AGAAAGGAAGTGGCC[G/T]GCAAGGTGAAGGCAG | 10580 |
rs112883639 | snp | A/G/T | 0.000638076 | 0.0178505 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384374 | TCCACAGTCTGGTAC[A/G/T]AGCATCCAGCCCCCC | 10580 |
rs112896548 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559168 | GATGACCTGATCATT[A/G]TCAATGCTGCACAAT | 10580 |
rs112939236 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512155 | AGGCGTGGTGGCTCA[C/T]GCTCGTAATCGCAGC | 10580 |
rs112943162 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521566 | TGGGATGACAGGCGT[A/G]AGCCACCATGCTTGG | 10580 |
rs112957062 | snp | G/T | 0.0562677 | 0.159906 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499144 | CAGTGCCATAATCTT[G/T]GCTCACTGCAACCTC | 10580 |
rs112957407 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328048 | TTGGCTTAAGGGAGG[C/G]AGCACTCTACTCATT | 10580 |
rs112961769 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336353 | ATCCAGTCCTGGCAC[C/T]TGAATTCATGTCCTC | 10580 |
rs112964801 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491886 | TACAACACTCCCACT[C/T]TACATGAATTAAATG | 10580 |
rs112985216 | in-del | -/TCTG | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378716 | ATCCCTCTTTTAATA[-/TCTG]TCCGTCCTACTACAT | 10580 |
rs112990128 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553128 | TGAGGCAGGAGGATC[A/C]CTTGAGCCCAGGAGG | 10580 |
rs112999904 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413967 | ACCCAACTCTCTCAC[A/C]AAAAAAAAAAAAAAA | 10580 |
rs113006519 | in-del | -/CCAGGA | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435375 | ACCCAAGTGCACAGC[-/CCAGGA]CCAGGACCCCAATGC | 10580 |
rs113041316 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492599 | CCTGTGTTATGGGAG[C/G]ACTGAGCAGGGGCAC | 10580 |
rs113041828 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355170 | AACTAGTTTAATGCA[A/G]AGAAAACTACTCAAA | 10580 |
rs113057825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457948 | GAGACTTCACCACTA[C/T]GTAATATATCCATGT | 10580 |
rs113086931 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482175 | CCCACAGCAAAACAC[A/C]CCCTGCAGCCTCCAT | 10580 |
rs113110471 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421238 | GAGAGAAGTAGTAGT[C/T]GACTCCACAGATGTG | 10580 |
rs113118255 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431523 | GGGCTGTGCAAAGTC[A/G]TCCCTGGAGAGGCCA | 10580 |
rs113123438 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483795 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATCAG | 10580 |
rs113132259 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327054 | ACTAGACAATGCCTC[C/T]CTGAGCCCTCCCCAG | 10580 |
rs113141429 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530122 | CTGTCACATAGAAAG[C/T]CTTCATGAACTCTTT | 10580 |
rs113148893 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357278 | TGCAAGGATGCAACA[A/C]CAAAAAAAAATGGCT | 10580 |
rs113149206 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506262 | ACATGTGCACACACA[C/T]ACACACACACACACA | 10580 |
rs113154313 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368041 | GGGCAATGGCCCACC[A/G]TGGGCCAACATGCTT | 10580 |
rs113161506 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504482 | GCAGACATCTGTCTT[C/T]AAGTGATTGCAGTTG | 10580 |
rs113172774 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360820 | AGCTTTGGCCAGAAC[-/T]TTTTTTTTTTTGAGA | 10580 |
rs113185181 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555534 | AAAGCAACTTAAATA[A/C]TTTTATACTAAAACC | 10580 |
rs113198375 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460746 | ATTAATAACTTTATA[C/T]AGAGTACAGCCAGAA | 10580 |
rs113198764 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367076 | TGGGACACAGTCTGG[C/T]TCTTTCACTCAGACT | 10580 |
rs113202231 | snp | C/T | 0.444444 | 0.157135 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513387 | TGTCCCAAGCAGCAG[C/T]TGGCCAAACACACGT | 10580 |
rs113206350 | snp | C/T | 0.116138 | 0.211142 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325570 | TTTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTGA | 10580 |
rs113206391 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466769 | GAGAAGGAAGCAAAT[A/G]GCAAGAAAGGTGGAT | 10580 |
rs113217022 | in-del | -/A | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558455 | TCAGTTTGGCGGGGA[-/A]GGGGGAGGAACATGG | 10580 |
rs113220154 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441210 | ACACCACACAATGCA[A/G]TTGATGAATGGCAGG | 10580 |
rs113221339 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424022 | AAGGTTCCAAGTGAT[G/T]GGCATTCACGTATAG | 10580 |
rs113224726 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335743 | CTTCTGAGAAGTTGC[C/T]GAAAGTCTTTGACTT | 10580 |
rs113228108 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347455 | TCTTTTTTTTTTTGA[A/G]ACAGTGTCTTACTCT | 10580 |
rs113247077 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434461 | CACACAGACATTCAC[A/G]TACACAGAGGAAGTA | 10580 |
rs113247690 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525732 | TTTTCCAGTCTTTCG[C/T]TACCACAAACAATGC | 10580 |
rs113256146 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346472 | ACATAAGAAACAATG[A/G]CAAGTTAAAATCAGG | 10580 |
rs113264806 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520816 | AATGCCTGGGGGCCT[A/G]AGAGAATGCAGAAAG | 10580 |
rs113273931 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367252 | GGGTCTATGTTGCCC[A/G]GGCTGGTCTTGAACT | 10580 |
rs113280018 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95317803 | CAAGGTGGGTGGATC[A/G]CCTGAGGTCAGGAGT | 10580 |
rs113283950 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502589 | CCCAGATAGAACAGA[C/G]CAGTGTCGCCTGAAC | 10580 |
rs113288919 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437142 | CACTGTTTATTACAG[A/G]TGAAGGTAAAAGGCT | 10580 |
rs113290448 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396504 | ATCCAGGTGAGAACA[-/T]TTTTTTTTTTTTTTG | 10580 |
rs113291349 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413649 | TCCCATATTACAACT[C/T]GCAATGAAGTTATCA | 10580 |
rs113309814 | snp | A/G | 0.0202857 | 0.0986476 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399003 | AAGAAGGACCTCTAA[A/G]TCAATATACATACCC | 10580 |
rs113319494 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442662 | AGAACTGTGAGCCAA[C/T]TAAACCCCTTTTCTT | 10580 |
rs113323915 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554321 | AGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 10580 |
rs113340726 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390651 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGACAGAGA | 10580 |
rs113344127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328582 | TACATATTCAAGTGT[A/G]AAGAAACCAAAGGCT | 10580 |
rs113365825 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361702 | CCTCATGATCCTCCC[A/G]CCTTGGCCTCCCAAA | 10580 |
rs113377948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386564 | TTGCTTGAACCCCAG[A/T]GGCAGAGGTTGGGGT | 10580 |
rs113387284 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466879 | ACTCCAACTCCTATA[A/C]TTCCTACATATTATC | 10580 |
rs113399837 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460750 | ATAACTTTATACAGA[C/G]TACAGCCAGAAACAA | 10580 |
rs113403011 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426850 | AGTGGTTTTGTGAAT[A/C]CCCTGAACTTGCAGC | 10580 |
rs113407340 | snp | A/G | 8.24069e-05 | 0.00641846 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336674 | TGAGAGTCTCTGTTC[A/G]GTACTCAGGCACCTG | 10580 |
rs113411899 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363022 | GTTTCATTTTATAGC[C/T]TTTTGTACTGCATGA | 10580 |
rs113413559 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555363 | CAGCAGGAAAGCATG[A/G]AGGGGTGGTTCTCAG | 10580 |
rs113441837 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415064 | AACCCCATCCAACTC[C/T]GCTTTTCATCCATCT | 10580 |
rs113458334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393947 | ACATTTTAGAAACTT[C/T]CTTGACATTTAGACT | 10580 |
rs113468514 | snp | C/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354594 | GTTTCTAGCTTACAG[C/G]GCATTAAGTGCAGCA | 10580 |
rs113480611 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365097 | TTGTTAAAATGATGT[C/T]ATTCGATACCTGTGC | 10580 |
rs113490020 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386573 | CCCCAGAGGCAGAGG[C/T]TGGGGTGAGCCAAGA | 10580 |
rs113492215 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383731 | ACTCTTAACTTGGCT[C/G]CCATACTAGGAGCTA | 10580 |
rs113516055 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557200 | ATTATCACCTTTTAT[C/T]CTTGCCTTTGAATGG | 10580 |
rs113517301 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476063 | TCTTTTTTTAAAAAA[A/C]GATAAGGTGGCAGTT | 10580 |
rs113528723 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381062 | TTCACAGAAGAGGCC[A/G]CTTTTCCAGGGTGGT | 10580 |
rs113540286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394325 | CAAAGCCTTGGGTAG[C/T]TGGGTAAAGGCAGCT | 10580 |
rs113545816 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558237 | GAGGCTGCAGTGAGC[C/T]ATGATTGTGCCACTG | 10580 |
rs113563634 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342850 | TTCCTTTGCTTGCCT[C/T]AATAATGATGATGTT | 10580 |
rs113563699 | in-del | -/AC/ACACAC | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554692 | AGAAACTCTCTGTGT[-/AC/ACACAC]ACACACACACACACA | 10580 |
rs113565548 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547295 | ACGCACTGTATCATA[C/T]TAGAACCTTCCTATT | 10580 |
rs113569566 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364583 | GCCTGCTGAGTAGCT[C/G]GGACTACAGACGTGC | 10580 |
rs113590270 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449247 | AGATGAAGAACTCTT[C/T]TATTTTGGAGACAGA | 10580 |
rs113591815 | in-del | -/C | 0.0387552 | 0.1337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337650 | GACACATTGGAAGCT[-/C]CCCATCCCAGCCAAC | 10580 |
rs113601178 | snp | C/T | 0.243919 | 0.249926 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499217 | AGCTGGGATTACAGG[C/T]GTCCACCACCACGCC | 10580 |
rs113618301 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348346 | GGTTACCTCATGTCA[C/T]CCAGCTGTAGAGCTG | 10580 |
rs113627063 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370313 | GGCTGGAGTGCAGAG[A/G/T]TGTGATCTCAGCTCT | 10580 |
rs113644380 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330791 | GCTGGGATTACAGGT[G/T]TGAGCCACCACGCCC | 10580 |
rs113644934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327310 | CCTTTCCCCCATTAA[C/T]AGGAAGCAGGTGACA | 10580 |
rs113702575 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321028 | CATCTCTTGTTGCCC[C/T]TCTCTGTCTCTGTGG | 10580 |
rs113703525 | in-del | -/A | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447160 | CAAAAACAAACAAAC[-/A]AAAAAAAAACAAAAA | 10580 |
rs113705956 | in-del | -/AC/ACAC/ACACAC | 0.490343 | 0.0688145 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502998 | CACATACACACACAA[-/AC/ACAC/ACACAC]ACACACACACACACA | 10580 |
rs113707876 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347744 | CCCGGCTGTGGAATT[C/T]CTTTCTTTTTTTTGA | 10580 |
rs113713537 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331690 | TTAAATGCTACTTTT[C/T]TGAGGAGAGCAAAAT | 10580 |
rs113713804 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538778 | TGAGCCCAGGAGGTT[A/G]AGGCTGCAATGAGCT | 10580 |
rs113757011 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449180 | TATTTTATTTTCTGT[A/G]GTTACACTGGCTAGA | 10580 |
rs113759537 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400233 | GAAACTATTATCACC[-/T]TTTTTTTTTTAATAG | 10580 |
rs113767401 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353238 | GACTAGGGCTTATAT[A/T]ACTAAAATGGAATTT | 10580 |
rs113778455 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362708 | CAACAAACACGCATT[A/G]CTCCCCCAGTCTCCA | 10580 |
rs113792708 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441465 | AGCTACACGAGTGCA[C/T]GTGGTTTAAAGAGAG | 10580 |
rs113802321 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95317811 | GTGGATCACCTGAGG[C/T]CAGGAGTTCAAGACC | 10580 |
rs113810290 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559650 | TGCCTTGGGCAAAGG[A/T]GCCAACAGACCAACC | 10580 |
rs113811059 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400126 | ATAAATGCTTGGGGG[C/T]CTCTGGACTACTGAG | 10580 |
rs113828457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400631 | AAAGTGATGGCTGAC[A/G]CCAGGGAGATGGCAG | 10580 |
rs113828792 | snp | A/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419265 | CCAGCCAAAAAAAAA[A/C]CAAAATGAATAGCCC | 10580 |
rs113843883 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394924 | AAATCTAAAAGCCCA[A/T]ATCTTATGCCTACAA | 10580 |
rs113848173 | snp | A/G | 0.0349115 | 0.127424 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562352 | TGGGGGGAAGGCACC[A/G]TGTTAGATGGGGTTC | 10580 |
rs113857483 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345068 | AATTCAAAGAAATAA[C/G]TGTATTAATTAAATT | 10580 |
rs113888101 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528657 | GGCGCAGTGGCTCAC[A/G]CCTCTAATCCCAGCA | 10580 |
rs113891857 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427397 | GCAATGAGGTCAGGA[A/G]GCAGGGATAAGGTGA | 10580 |
rs113903069 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541329 | CTCTTTCCCCAACAG[C/T]GGGTACCCCTCCTGT | 10580 |
rs113922123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503310 | CAGCTTCAGAAAAGA[C/T]GCTCTTTATATCCAA | 10580 |
rs113922839 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360002 | GAGGAGATGGAAGAA[C/G]CTGAGGGTAGCTTGC | 10580 |
rs113935941 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314477 | TGCATCAGGTGCCTC[A/T]GTTTTGCCTCTGTTT | 10580 |
rs113963399 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388735 | ACACAGGGTAAACAA[C/T]TCACTTAGGCCTCTG | 10580 |
rs113967860 | snp | A/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559960 | CGATCACCACCAAGA[A/T]ACCTTTCCAACCAAA | 10580 |
rs113976023 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464391 | ACTGGCTATGGAAAC[C/T]TGGGCAAATTATCTT | 10580 |
rs113980445 | snp | A/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334386 | AGCAGCCCTTTTCAC[A/G]CAAATGCCAGCTCTC | 10580 |
rs113991965 | snp | C/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539731 | TGGGTGTTCAATAAA[C/T]GTTAGTGATTATTTA | 10580 |
rs113997378 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404798 | GAATCTCATCTGATC[A/G]TCATACAACCTGGGA | 10580 |
rs114059148 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544908 | GCAGCTGTCTTGATG[A/C]GAAGCCGTATCTTCT | 10580 |
rs114082097 | snp | A/C | 0.000477756 | 0.0154483 | missense | SORBS1 | GRCh38.p7 | 10:95341346 | TTAGCAATAGCTTCT[A/C]CATATTCCAAAACCT | 10580 |
rs114088633 | snp | C/T | 0.0170251 | 0.090679 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336798 | TGTCCACTCTCTTCG[C/T]GCCATGGCTGCCTCT | 10580 |
rs114115242 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516992 | GAGAGGCAGAGGACA[C/T]AAGAGTGTTTGGCAA | 10580 |
rs114124737 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427805 | GCACTCTTCACAAAT[A/C]CCCCCAACTCCATGA | 10580 |
rs114133761 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320182 | ATCCTGGTGCCCCAC[A/G]CTCAGCCAAGAGCTC | 10580 |
rs114151536 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316066 | AGAACCTTGCCTAGG[A/G]CCACATAGCTAGTTA | 10580 |
rs114176388 | snp | A/C | 0.040671 | 0.13668 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369105 | CATCACATCCACTGA[A/C]CTTCCTGGGAGTCCA | 10580 |
rs114176887 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324446 | TGCAGGACTAACTTC[C/T]GTTGCAGGCATCATT | 10580 |
rs114180280 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456489 | GACCCCTCCATAATC[C/T]AGGACTTCCCAGCCT | 10580 |
rs114184529 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505282 | CCACGTTCTGCGGGA[C/T]TCCGTGGGAGTGGGC | 10580 |
rs114255671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389551 | TAGCTGGGATTACAG[A/G]TGTGGCAATCAAGTT | 10580 |
rs114260625 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514780 | AGCAGGAACCAAGTA[C/T]GGGCTACAAAAGTCA | 10580 |
rs114263837 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391129 | CAGTATAGCAGCGTT[A/G]AGTAAAAGCCTGTGT | 10580 |
rs114265197 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473127 | TGAGACAGACCACCT[A/C]TCCTACAGTAGATGT | 10580 |
rs114273288 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484961 | CCGGGACAACAGTGC[A/G]AGACCCTGTCTCAAA | 10580 |
rs114274013 | snp | C/T | 0.115088 | 0.210473 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382535 | CTAGCTTCACCCTTC[C/T]GCATAACCAGTTTTC | 10580 |
rs114288609 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352526 | CATCAAATGGCTGTG[C/G]GATTTCCAGTACTCA | 10580 |
rs114290141 | snp | A/G/T | 0.00411716 | 0.0451856 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414559 | CCTCCGGGGCAGGAG[A/G/T]GACCAGCGGAGGTGG | 10580 |
rs114299047 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327474 | AGAAATCCCCCAGAA[A/G]TCAGATCTTAGCCTC | 10580 |
rs114306891 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324933 | CTGTGGACTATGACT[A/G]ACTGGGATATTGTAG | 10580 |
rs114307999 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317465 | CGTCAATAAAAGCAT[A/G]TCAAACACAGTGTCT | 10580 |
rs114311670 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362322 | TGTTTAAAAACTTGC[A/G]AACAGTCTGTTTCTC | 10580 |
rs114334539 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431615 | CATGATACACAGCAC[C/T]TCATACACTTCTTCC | 10580 |
rs114369032 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440694 | AGCAAACTACTCTAC[C/T]AGCCTAGATGAAGGA | 10580 |
rs114371532 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370169 | TCTGCTTAAGTGTGG[C/T]ATGGGTCCATCAGCA | 10580 |
rs114373081 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489185 | CTATTCCCTCTGCCT[A/G]AACACTTCTCCTCCC | 10580 |
rs114376969 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378026 | TATGTCAAACAGCGA[C/T]GGGTGAGAGCAACCA | 10580 |
rs114378292 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406202 | AGCACATAGTAAGAC[C/G]AAGAAGCCCTGGCAT | 10580 |
rs114384529 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463874 | CAAGGTGAGAGAACC[A/C]TCAGGAAATGGGTCC | 10580 |
rs114387826 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395784 | CACGCTCATCCACCC[A/G]ACCACAGCGGATTTA | 10580 |
rs114433316 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437781 | CCTGGAGCTCCCCTC[A/G]GATGTCATGTCCTCT | 10580 |
rs114438219 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508885 | TCCAGAACTCAGAAG[A/G]GCCATAAATAGAGAG | 10580 |
rs114459629 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359340 | GGCTGGAACTTGAAC[C/T]AGGCCATTGAGCACT | 10580 |
rs114482453 | snp | C/T | 0.0050467 | 0.0499788 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437452 | ACCTTTAGAAATGCC[C/T]TCCAGTACCAATCCA | 10580 |
rs114483964 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549986 | AGCTAGGCTTGTTCT[C/T]CAAGCAGGGTCTGGG | 10580 |
rs114484929 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357871 | AGAATAGGAGTTAGT[A/G]CTTTTAACATTTTTC | 10580 |
rs114494406 | snp | C/T | 0.0390878 | 0.134224 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336600 | TGCTCAGCCTCACTT[C/T]CTGGAAAAGCGCTAC | 10580 |
rs114506378 | snp | G/T | 0.100588 | 0.200439 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483566 | TCTTGCTGCCCAGGC[G/T]GGAGTGCAATGCAAT | 10580 |
rs114562706 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445682 | TGAGGCTGACCAGAT[C/T]TGAATCCCAAGTGGC | 10580 |
rs114563132 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336751 | CACCAGGGCCTCTTT[C/T]GCCTGCCCCCCTCTC | 10580 |
rs114586518 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342769 | ACATGGAAAAGTGAT[A/G]TTGGAAAGAAAAGTA | 10580 |
rs114633792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400353 | ACCTGACTCTAGCAG[A/T]CCTCTCTGAACCACA | 10580 |
rs114635227 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369200 | CGCCTCTGTGAACTC[A/T]CCTTTCTCTCCCTCT | 10580 |
rs114658889 | snp | C/T | 0.0333238 | 0.124705 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315681 | GGAGCATTGAGCCAT[C/T]TGGGAACAAAGCCCT | 10580 |
rs114663246 | snp | A/C/G | 0.00993785 | 0.0698258 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552890 | GGGAAGTCTCCAAGC[A/C/G]GGCGTAAAAAAAAAA | 10580 |
rs114673058 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326046 | GTGGCTGGGACCTGA[A/C]CTTGTGAAGTTTGTA | 10580 |
rs114676366 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329011 | AGTTAGTATTGGAAC[A/T]TCTGTCTCTCAGACT | 10580 |
rs114676705 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500987 | CCCTTCTTCCTTCCC[C/T]GCCTTCCTTAAGGAC | 10580 |
rs114679071 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389122 | TCCAAATATTAATGG[C/T]TCATTTTTGACACAA | 10580 |
rs114681041 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357479 | TGGCCGGTAAGAAAA[A/T]AGGGGAGGGAATTTA | 10580 |
rs114683360 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362621 | TCCTGCTTCTTCCCT[A/G]TCTTTGACACAGCTC | 10580 |
rs114686164 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410501 | TGAGAGTGAGTAAAC[C/T]GGGGCAAATGGCCTT | 10580 |
rs114686288 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380866 | TATTTTAATAAAAAC[C/T]AAACTCCAGCATAAT | 10580 |
rs114697327 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311353 | TGCATTTTCGCCCAC[C/T]CATACCAAGAGAGGA | 10580 |
rs114700580 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550177 | GTACAAGGCACTGAA[C/T]TAAGCCAGGAGAAAG | 10580 |
rs114710319 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445134 | AGTATGACGATAGTA[C/T]GTGACAATGACAATG | 10580 |
rs114748499 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373214 | TCATCTCTGCACATG[A/T]ATATTCCGCATTTCA | 10580 |
rs114884613 | snp | C/G/T | 0.000477972 | 0.015452 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95434656 | TGAGGCGTTTTTCAC[C/G/T]GTCTTCACAGGAATG | 10580 |
rs114884933 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411814 | TCAGCAATGTTGTGT[A/C]TGAGCAAATGTTTGT | 10580 |
rs114918019 | snp | A/G | 0.00921639 | 0.0672551 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95372011 | TCTAGGAAGGATAGA[A/G]CAGTCTCCAGGAGTA | 10580 |
rs114921804 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385028 | AGCAAATCAAACTCA[C/T]GCGTGTCTCTATGGT | 10580 |
rs114933500 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546647 | CACCAGGCCCCCCTC[A/C]AACATTAGGAATTAT | 10580 |
rs114935822 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529164 | AGAAAAGGGAAGCCA[A/G]TCATATACTCCAAAG | 10580 |
rs114945741 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376645 | AGGAAACCATGTCCC[A/G]TACACAGTAAAGTGA | 10580 |
rs114951395 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546508 | CAAAAGAGCAAAGAG[A/G]GAGGGGCTGCACACT | 10580 |
rs114954324 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95395059 | CGTAGGGAAATAAGG[A/G]TTTTCTTCAGGAGTG | 10580 |
rs114967103 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407077 | GGTACTGTCATCATT[C/T]CCCTTGGCTGCGTTC | 10580 |
rs114971097 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412165 | ACTGCCTGAATGCAT[C/T]CAAGAAACACAAAAT | 10580 |
rs114977052 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389996 | TTACAAATCCTGTAA[A/G]GCCAGTAGAGAATTA | 10580 |
rs115026657 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342821 | TGTACCCCTTTGCAA[C/T]GTTTCCATATCCATT | 10580 |
rs115028864 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323780 | ACTGCTTGAGCCGGG[A/G]AGTTGGAGACCAGCC | 10580 |
rs115074895 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325164 | ATAGTATGCCAAGAC[C/T]GGTGGTCTGGGTCAC | 10580 |
rs115082581 | snp | A/G | 6.60317e-05 | 0.00574556 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351366 | AGTCGTCTCTGGTCC[A/G]CTAAAAGTTTCTGCC | 10580 |
rs115101819 | snp | C/T | 0.040671 | 0.13668 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381296 | CATTCTAGTAACTTG[C/T]ACAAAATTTATGCCT | 10580 |
rs115109152 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490623 | AAAAAGTGTGTTAAT[A/G]AAGTTAATAAATGTA | 10580 |
rs115113618 | snp | C/T | 0.00317452 | 0.0397137 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336776 | CCTCTCTGCTTTCCT[C/T]TCATATTGTCCACTC | 10580 |
rs115148654 | snp | A/G | 0.00019769 | 0.00994012 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351287 | AGTGATAAACTGATG[A/G]TGCGTCGGAATGACG | 10580 |
rs115167368 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374402 | TGGGCAGAAATGTGT[A/G]GATTCTGAAACAGAC | 10580 |
rs115169301 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365458 | AGAGGTGGCCTGGGG[C/G]ACCAAGGAGAGCTTG | 10580 |
rs115174308 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450452 | GGGAAAAGACTTCTC[A/G]TAAGATTAGGTGACT | 10580 |
rs115177527 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457243 | AGAACACACCATGTT[A/G]GAAGAAAAGAACTAT | 10580 |
rs115213635 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362133 | TTCAAGGGGATTCAA[A/C]AAAAACACACTCACT | 10580 |
rs115280414 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369243 | TTCCACATCACCCAA[C/T]GTCCCCATGGGTAGT | 10580 |
rs115282883 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337744 | CATGGCCCTTCCCTG[A/G]GGTTTTATTTTCTCT | 10580 |
rs115307631 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315804 | TGTATCATCATTATC[A/G]TTTCTTTAGCAGACA | 10580 |
rs115340034 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350350 | GAGATCATCTTCAGC[A/T]GCGCTACTTAAGGGT | 10580 |
rs115342107 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365928 | GATCACTACCCTAAA[A/T]AGATTAAATTTTTCC | 10580 |
rs115345189 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395806 | GCGGATTTACTCTTC[A/G]TTGGAAATGCTAAAC | 10580 |
rs115361731 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515097 | CTTGTCAGCAGACTG[A/C]AAAGCAGGTCCAATT | 10580 |
rs115368433 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327856 | CCAGGTTCCAGGCCA[C/T]GCTCTGTACTAACTG | 10580 |
rs115395530 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556098 | AAGTCTAGAAACAGG[C/G]TACATCCCTTGAGAG | 10580 |
rs115410539 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453797 | CGTATGTGGATGGCC[A/T]ACTTTTCCTATATGT | 10580 |
rs115442765 | snp | A/G | 0.000124867 | 0.00790051 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414594 | GAGAAGGATGGTGGC[A/G]TCTGGCTAATGGGGG | 10580 |
rs115444055 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431275 | TGCACTAGCAGCATC[A/C]GCATGAACCTGTCAG | 10580 |
rs115477882 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351239 | CCTTTTTGCAGTATC[A/G]TCTATATTGAGGAGG | 10580 |
rs115509248 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445787 | AAATTGAGCTTGACC[A/G]GAACACTGAAAGCTT | 10580 |
rs115535936 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459539 | GAAGAAAAGGAGGAG[C/G]AGGCGGGCTCCGGAA | 10580 |
rs115553579 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363217 | CCCTATTACACCTGG[A/C]ACCCCTTGAGGGCAG | 10580 |
rs115555421 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347028 | ATGCCCAGGTCCAAG[A/T]CAGCCTCTGCCCCTT | 10580 |
rs115618845 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343244 | AAATTTTAAACAAAA[C/T]GAAAAAAGAAGGATA | 10580 |
rs115657645 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442557 | TCTTGTCGTGTGACA[C/T]GCCTGCTCCCCCTTC | 10580 |
rs115671918 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352386 | GAATTAGAATGGATA[A/C]TTCTTAGCATTGGAA | 10580 |
rs115675824 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456681 | GACTGCCTGTGAGCG[A/G]GTTGGGCCACAAGAG | 10580 |
rs115679609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327425 | GGGTGACCCTGCATG[C/T]GTCCTTGCTGTTGCC | 10580 |
rs115682063 | snp | C/T | 0.00200872 | 0.0316279 | missense | SORBS1 | GRCh38.p7 | 10:95381752 | CTCTTGGGCTCTGCA[C/T]GATATTTTCTTGTGT | 10580 |
rs115683815 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389277 | AAAGACACAGATGTA[C/G]AGTTGGGTACTGAGT | 10580 |
rs115686502 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95399182 | CACTCTTCTTTCTGA[A/G]ACAGGATCTGGAAAT | 10580 |
rs115689192 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404064 | TCTGCATCTCCTAAC[A/G]TATGGCTGGAGGCCT | 10580 |
rs115742817 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548427 | TTACTACTTATGTGT[C/T]ATGCATAGTTCTTTT | 10580 |
rs115777407 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537504 | CGCCCCTGGGTAGAG[C/T]GGGTACTCAACAAAC | 10580 |
rs115844060 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439336 | CCTCCTTCCAACCCC[C/T]CACCTGAGAGAGAGA | 10580 |
rs115851651 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508674 | CTCCTAGAGAGTGAG[C/T]TCCTCATTGCCAGAG | 10580 |
rs115940985 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545020 | GTACCACGTCCAACA[C/T]AGAGGCCCTGCAAAG | 10580 |
rs115965339 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534920 | CACCCTCGGCATATA[A/G]CTATCATTGCAGCTA | 10580 |
rs115972557 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445952 | GCCTGATTTGGTTGA[C/G]TACATGATGGCACGT | 10580 |
rs115975295 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471361 | GTAAAGGCAGAAAAA[G/T]CGCACTGGTAAATCA | 10580 |
rs116022679 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337557 | GGAAGCAGTGAGAGG[A/T]GTGGAGATGGGGAGA | 10580 |
rs116024654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362834 | ATTAAGTGTCAATCG[C/T]TCTCCTAGGTGAAGA | 10580 |
rs116060550 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432686 | GATGAACCTGGTTAC[A/C]GCCATGCGAAGTCTT | 10580 |
rs116076394 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378138 | AGTATAACTCAGCTG[C/T]GGATCCTGTTATGGA | 10580 |
rs116082918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401201 | GCCTGGGCAACATAG[C/T]GAGACCCCATCGCTA | 10580 |
rs116086048 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397663 | TATCATGCTGTGCCC[C/T]CAACCATTCTAGATT | 10580 |
rs116089386 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378023 | GGTTATGTCAAACAG[C/T]GATGGGTGAGAGCAA | 10580 |
rs116090883 | snp | G/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442366 | TAGATATTTGTCCCT[G/T]CCCAAATCTCACATT | 10580 |
rs116096246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453828 | GAGTACTGCAGGGCC[C/T]GCTGCAGGACATAAG | 10580 |
rs116101258 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358591 | GGCACAGAAAAAAAA[A/C]TCAAGGGTACTTACT | 10580 |
rs116106042 | snp | A/C | 0.0368353 | 0.130617 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314357 | AGAAAACAGACATAA[A/C]CTATCTGCTTGGCCA | 10580 |
rs116112696 | snp | A/G/T | 0.00954057 | 0.0684251 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516695 | TCCCCACGCTCCACA[A/G/T]GTATACTGGCCACAA | 10580 |
rs116134601 | snp | C/T | 0.104504 | 0.2033 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320440 | GCTGGAGTGCAATGG[C/T]GCAGTCTTGGTTCAC | 10580 |
rs116135601 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352903 | GATGCTTGAAACTGC[C/T]ACAGTTCTTACTCAA | 10580 |
rs116136934 | snp | C/T | 0.0116941 | 0.0755665 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356827 | CTTGGAGGGGGAGGC[C/T]TCTTTTGGAATCATT | 10580 |
rs116186433 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360778 | GCAGCTTCCATTCTG[C/T]TGTGCCTGCTATCCT | 10580 |
rs116187824 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365377 | AGGTGAGGAGGTAAA[C/T]GAGGAGAGCAGGCAG | 10580 |
rs116196907 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435266 | AAGCAAATCAAAGCC[C/T]CCATCTGTTAAACGG | 10580 |
rs116198461 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373165 | AATCTGATTCCAAGG[A/T]GTGTTCACCACTGAC | 10580 |
rs116207878 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514572 | TGGTCACTCCACCCC[A/G]GAAACATCACGGTGA | 10580 |
rs116215092 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544329 | AGAACAGGTGGGCTC[C/T]TGGCCTCCCAGCCAG | 10580 |
rs116217419 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468109 | TCCATATTGTTCTGG[C/T]TGGTCGCGAACTCCC | 10580 |
rs116221211 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358749 | ACACACACACACACA[C/T]ATTTCTCAGTTAAGT | 10580 |
rs116221393 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400923 | AGGCAAGAGAGAAGT[C/T]ACAGGAACACTCTGA | 10580 |
rs116222803 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406551 | CAGTGACCGTCTCCT[A/G]AGAGCTTGCTAAATG | 10580 |
rs116231721 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527474 | TAAAATAATTCAAAA[A/C]ATAAAATGAACTGAC | 10580 |
rs116250790 | snp | C/T | 1.84079e-05 | 0.00303375 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336533 | TACCTGGCTCCCACC[C/T]CTCCGAGCAGCTTTC | 10580 |
rs116266444 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546208 | CTGTTATAAGCTAGA[A/C]CACCACCCAAGATGA | 10580 |
rs116273396 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327701 | CTCTAGAAACAGCAC[A/G]AGGCTCTGCTGCTCC | 10580 |
rs116295732 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437211 | CCAGGCATGAAATAC[A/G]CCTTGGTCCTCGTAT | 10580 |
rs116296222 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475105 | TTAAACTGGCTGCCT[C/T]AGTAAGCCCCAGAGA | 10580 |
rs116299420 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471074 | TTGTGAGTGGGCCAT[A/G]GCAAAATGCTTCAAA | 10580 |
rs116304255 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383166 | AATAGCATGAGGAGA[C/T]TGCTTCAGAGGGCAT | 10580 |
rs116324798 | snp | C/T | 0.000601576 | 0.0173328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356090 | GCGGGTGTATGAGGC[C/T]GGGCAGGTGCCCTTG | 10580 |
rs116385267 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348019 | TACAGGTGTGAGCCA[C/T]TGTGCCTAGCCTTCC | 10580 |
rs116386610 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352549 | AGTACTCAAATAAGT[G/T]GTAAAGATTAAATTA | 10580 |
rs116388913 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438561 | GAAGGCTAATTCTCC[C/T]AGATGTCTGAGTCTC | 10580 |
rs116411747 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502509 | CCACAGAGCATTTCC[C/T]CCATCACTCACCTTC | 10580 |
rs116419273 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375597 | CTTCTCAGTGTGTAA[C/T]ACATTTTCAGCTTGT | 10580 |
rs116422676 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429558 | TTCTTTGTTTCCTCT[A/C]CTCAAACCCAGCTTG | 10580 |
rs116438692 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511729 | TTTCTAGAGGAGAGA[C/T]GGCTAGTAGGAAGAG | 10580 |
rs116445956 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555435 | GTTGGGGTATGAGAC[C/T]GATATGCATATTTAC | 10580 |
rs116447903 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392413 | ATCTAGGCAGGAGTG[A/G]GGGCGTGAGATGGAA | 10580 |
rs116498221 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366183 | CACAGATGCGATGGT[C/G]ACAAAATAAGAAAAG | 10580 |
rs116523896 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378071 | AGCTGCCCAGAGATA[A/G]AGCTAAAAAGGTGAT | 10580 |
rs116531064 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441826 | GGGAACCAATCCCTG[A/T]TGTTCAAATGGATAA | 10580 |
rs116635703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444260 | CCACCACACCTGGCT[A/G]ATTTTTAAAATTTTT | 10580 |
rs116648282 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421054 | CACCTATAATCCCAA[A/C]ACTTTGGGAAGCCAA | 10580 |
rs116654878 | snp | C/G | 0.000314614 | 0.0125383 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371398 | CTCTAACTCTGTCTG[C/G]CAGAGGCTGAGATCT | 10580 |
rs116663923 | snp | A/C/G/T | 1.64806e-05 | 0.00287054 | missense | SORBS1 | GRCh38.p7 | 10:95432513 | CTTGGGGTTTCCCTG[A/C/G/T]AGGAAGACGAGGCCC | 10580 |
rs116664131 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549796 | TAACAAGTCTTTCTC[C/T]GCTCCACTGTGCTGT | 10580 |
rs116696507 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390956 | TGGGTCCCTAACTAT[A/G]TATTTCCAGGCACCA | 10580 |
rs116708155 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321096 | TATACTCACTTCCAC[A/G]GTTACAAAATGCCCA | 10580 |
rs116711450 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400083 | CAGACTCACAGGAAG[C/T]GAAGGGTGCTCCAGA | 10580 |
rs116739056 | snp | C/G | 0.040671 | 0.13668 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369979 | TGGCTTCCTCATGCT[C/G]TGCTGTCTCTGGATC | 10580 |
rs116760076 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551602 | ATGCATGGAAGGATA[A/G]CTGCAATGGAAGATA | 10580 |
rs116768871 | snp | C/T | 0.00143379 | 0.0267364 | missense | SORBS1 | GRCh38.p7 | 10:95384274 | TGGGAGAGTACAGAT[C/T]TGAATCATCATCTAT | 10580 |
rs116788142 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350849 | CCATAGCTACCAATG[C/T]ATATGGACTCAGGTA | 10580 |
rs116794412 | snp | A/G | 0.000988484 | 0.0222096 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351350 | TTCTTGCTCGCGTTT[A/G]AGTCGTCTCTGGTCC | 10580 |
rs116807305 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445589 | TGCCACCCAAGAACC[C/T]TGACCAGCAGAAGAT | 10580 |
rs116809223 | snp | C/T | 0.106987 | 0.205054 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498744 | CAGGCTGGTTTCAAG[C/T]TCCTAGGCTCAAGCG | 10580 |
rs116835606 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426632 | ACTGTCACACATCAC[G/T]GCTGGGAAATAATAT | 10580 |
rs116837924 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512939 | GATATTGGCAACTTC[C/G]GGGGTCAGGGCGAAG | 10580 |
rs116847634 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543937 | GTAACAAAGACCACC[A/G]AACCATAAGAGCCCT | 10580 |
rs116858656 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333276 | CCTTTGCTAGCCAAG[A/C]CTTGCTTTTCTCCCT | 10580 |
rs116871102 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317636 | TTCATGGTAGAGACA[C/T]AGGCTCAGTCAACAT | 10580 |
rs116871173 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342168 | ATTCCATCAATTTCA[C/T]CATTTGTCCACCCAT | 10580 |
rs116888462 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451880 | TTAAAAAGCTGAAAA[G/T]CAGTCTGTTAGAGCT | 10580 |
rs116913515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440678 | GCAAAGCAAAAGAGG[A/G]AGCAAACTACTCTAC | 10580 |
rs116922951 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511833 | GCCCCAGAAGACAAA[A/C]CCAAAGCTATCAGAG | 10580 |
rs116934895 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542736 | TGAGGAGGGGTCTAA[A/T]TCACATTAGGATAAA | 10580 |
rs116938535 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419357 | GTTTACAGACTAAAC[A/G]ATTCTAGAAACAAAA | 10580 |
rs116939437 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469012 | TCCTTCGTCATTGCC[A/G]ATGCTTTTCCAAAGC | 10580 |
rs116949337 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412481 | ACCTCTGTTACCCAG[A/G]GCCAAACCCGAAGCT | 10580 |
rs116950726 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442412 | ATGTTGGAGGTGGGC[A/G]TGGTGGGAGGTGTTT | 10580 |
rs116951106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480831 | CTGTACAGTACAAAG[A/G]GAGAGATGCATGCAC | 10580 |
rs117017454 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385719 | CTTCCCTCACTTTCA[A/G]GAATTTATCAATATC | 10580 |
rs117038907 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332812 | TACATTAGGTATCAC[A/G]GTCCCGCCTTTGGAG | 10580 |
rs117053350 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327897 | GAACAAAATGCTTAA[C/T]GTCTTAGGACTTCAA | 10580 |
rs117054051 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344185 | GTCTGTAGTTGTAGC[A/T]GATGGAAGACTACCA | 10580 |
rs117063016 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553097 | TGGTGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 10580 |
rs117065926 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350694 | ATCCACCTACATGTG[A/G]GCAGCAGCACTGTTC | 10580 |
rs117078827 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499255 | TTTTTGTATTTTTAG[C/T]AGAGATACATTTTCA | 10580 |
rs117098321 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493004 | CACAGTGGTAGAAAT[A/T]CTAAGCCTTCAGGCG | 10580 |
rs117107933 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337914 | CACTCTGTCCTATAA[C/G]ACAACAGGATGCGGC | 10580 |
rs117149533 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399396 | ATATTATTTATGGGT[A/G]CTTTTGCACTACGAT | 10580 |
rs117172622 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320667 | ACAGGTGTGAGCCAC[C/T]GCACCTGGCCTCACT | 10580 |
rs117214894 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365961 | TTTTCCACCAAAATA[C/T]CCAAATCCCTGCTGA | 10580 |
rs117215691 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534571 | TTGTGTGAATAAACC[A/G]TGAAGGCCAAGGGCA | 10580 |
rs117218202 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342252 | GGCAGATCTGGTCCA[A/T]AATCCAGTTCTGAAA | 10580 |
rs117228959 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391816 | GAGCTTTAGAAATGT[C/T]TTTTTTATACTGTAT | 10580 |
rs117245697 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333034 | ACATGGCTGTCAGAG[A/G]GCCAGCAAAAAGAGG | 10580 |
rs117273441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382143 | CATTCCACAGACATG[C/T]CTGTACTTCCCATTC | 10580 |
rs117300142 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549914 | TTTTAATACCAATGC[A/G]TTTGAGTCCCCCAAC | 10580 |
rs117312978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420971 | ACACAAGGAACACAT[C/T]TCTGCTATAGTTTTT | 10580 |
rs117340645 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527513 | TAGTGAGCTCCCTGT[C/G]CTTGGAAAGATGCAA | 10580 |
rs117365358 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385488 | TCCTTGTTTCTATGC[A/G]AATCATTTTAAGTTT | 10580 |
rs117414401 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315803 | TTGTATCATCATTAT[C/T]GTTTCTTTAGCAGAC | 10580 |
rs117428240 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490317 | AGAAAATGGTAGCTA[C/T]AGTGGTAGGAAGGGA | 10580 |
rs117429354 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541377 | TCCCAGGCTGGGACC[C/T]TGCAAATACCTCCAG | 10580 |
rs117439162 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493538 | TTTCTTCATAGATAA[A/G]AAAGAAGTGAGTCAC | 10580 |
rs117449139 | snp | C/T | 0.00398005 | 0.0444318 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336888 | GGCAGCTGCAAGAAG[C/T]TATCTTGGTGGATGC | 10580 |
rs117464253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404673 | GTACAAAGGAAGCCC[C/T]GAATACAATGGTAAG | 10580 |
rs117470835 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540929 | ACCCCTTCGTCAAAG[A/G]GTCTCAAAACCACCC | 10580 |
rs117481222 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481278 | TACACATCCAGGCCA[C/T]ACCTGCTGACACAGA | 10580 |
rs117496563 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460002 | GTTTCTCTGTAGGAT[A/G]TGTCAGGTCCACATT | 10580 |
rs117520475 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487674 | TCAAAATGGGAAAAC[A/T]AAGGCGCCCAACGAG | 10580 |
rs117535090 | snp | C/G/T | 0.0138852 | 0.0822049 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394396 | TAACACTGGCTACCC[C/G/T]GTTAATCATGTAAAC | 10580 |
rs117558126 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386924 | CAAGACCAGCCTGGG[A/C]AACATAGCGAGATCC | 10580 |
rs117586677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350870 | GACTCAGGTATAAGG[A/T]TTCTAAGCAGAATGC | 10580 |
rs117596279 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383711 | TCAATATTAATTAAG[C/T]CCATACTCTTAACTT | 10580 |
rs117629499 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403565 | GAGCCACCCTCATTT[G/T]TTTTTTTTTTTTTTT | 10580 |
rs117652622 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380877 | AAACCAAACTCCAGC[A/G]TAATAATTCCATCCT | 10580 |
rs117658070 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474956 | TAAGCCTGAGCTTCC[C/T]GCAAATGACATGGCT | 10580 |
rs117658883 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470464 | TAAGTGATTTGGAGG[A/C]GTTAGCAAAGGTCTT | 10580 |
rs117670953 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560649 | GATGCTGTCAGCCAC[G/T]CGGGGAGAAGAAGGG | 10580 |
rs117682723 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507423 | CTTGCACAAAACACG[A/G]TATTTTCCTCCTGGA | 10580 |
rs117684822 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382236 | CACACCCCTTGCTAA[C/G]TAGGTGATCTTAGAC | 10580 |
rs117699627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435362 | AGTCTCTGGGCAGCA[C/G]CCAAGTGCACAGCCC | 10580 |
rs117700419 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497187 | GCTGAGTGGGTGGGC[A/G]GGTAAACAAGGAGGA | 10580 |
rs117778203 | snp | A/C/G | 0.00407753 | 0.0449682 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336977 | AGGTGCTAGGGAGTA[A/C/G]GTTTTGTGTGGGGAA | 10580 |
rs117780663 | snp | A/T | 0.00115493 | 0.0240027 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339361 | AGAGGGTCCTTGTCC[A/T]AGCATGCCTCTGCAT | 10580 |
rs117781302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362556 | AAAGCTCAGGAAATC[A/G]GTCCCCTTCTCTCTC | 10580 |
rs117781353 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388538 | TATTTCTCCAAAGGC[C/T]CTTTAAAACAATGCT | 10580 |
rs117789121 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485118 | TTTATTGAAGTTAGG[C/G]TGCCTTGAACATAGC | 10580 |
rs117798260 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403855 | ATGAACCACTGCGTC[C/T]GGCCCACCCTCAAAT | 10580 |
rs117812273 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450043 | TACTTAACCCAACTA[C/G]TTAAAAAATATATTA | 10580 |
rs117854207 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369177 | GCTCCATCATTCGCT[C/T]TTCCCTCCGCCTCTG | 10580 |
rs117871681 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378508 | TTCTTTACACTATAC[C/T]ATATTCCCCTTTTCA | 10580 |
rs117898393 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500894 | TGGGCTGCTGCTGAG[C/T]GCACATAAAAGAAGA | 10580 |
rs117925568 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481095 | CAAGCACCCCCGGGG[C/T]CCCTGTACCTCCCCT | 10580 |
rs117925673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483386 | TGGTATTTTTGTGAG[C/T]AAATCACATTATACA | 10580 |
rs117952911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488457 | TATACCCTTTGCCTT[C/T]GTCTTCCCTCTTTCC | 10580 |
rs117994364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429768 | ACTTACCCACAGCCC[A/G]AAAGGAAGATGGCTG | 10580 |
rs118026752 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540569 | CTAGGTATTCAAAAA[C/T]ATATGCCTTCCTTTC | 10580 |
rs118055570 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513256 | TATACGCTACCGTTA[A/G]GTTCAACTGCACCCT | 10580 |
rs118112011 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445192 | GAGGACTTTTTGAGT[A/G]GCAGGTTCTGTTGTG | 10580 |
rs118112194 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509234 | GGTACCTTCTAGGAC[C/T]GCCCCCTTGCCCCAA | 10580 |
rs118128063 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476562 | CTTGCAAATAAAAGG[A/G]CCTAATGTCTTAGTG | 10580 |
rs118145062 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413440 | AGAATGCCTAGACCA[C/T]GGCAGAAACTCAATG | 10580 |
rs118167588 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495565 | GACAGGGATCCATAT[A/G]ATCATTTCTGCTTTG | 10580 |
rs118177351 | snp | A/G | 0.0019964 | 0.0315312 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558837 | AACAGGAAAGAACCT[A/G]AAAATGCCATCACAA | 10580 |
rs118191646 | snp | C/T | 0.0146769 | 0.0843982 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415435 | TTTTGAAAGAGACAG[C/T]AGAGAAGACACACAA | 10580 |
rs137869112 | in-del | -/C | 0.476052 | 0.106772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418092 | TTTTTTTTTTTTTTT[-/C]CCCGAGATGCAGTCT | 10580 |
rs137889169 | in-del | -/GT | 0.0103418 | 0.0711614 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440209 | AACACTGAGGTCAGG[-/GT]GTGGGCCTCAGCTAT | 10580 |
rs137891749 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491778 | TGGGAAAACAAAAGG[C/G]GCCTAGTTCCAAGAA | 10580 |
rs137900748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409985 | TCAGAGAAGCAGAAA[A/G]ACCAACCAGAAGCAG | 10580 |
rs137913911 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507649 | AGGCACGGTGGCTCA[C/G/T]GCCTGTAATTGCAGC | 10580 |
rs137919215 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379110 | TAGCTGGGCCAGGCA[C/T]GGGCTCATGGCTGTA | 10580 |
rs137938379 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382979 | AGGCCACTTAAGTTC[A/G]TGTGGTGCTTTTAAA | 10580 |
rs137958604 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543741 | CCCAGGATCTCTACC[A/G]AACCCAAAACATAAT | 10580 |
rs137961220 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455760 | AGCAACACGTTGAAA[A/C/T]CCCATCTCTACAAAA | 10580 |
rs137964668 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390991 | GGAGGTACTGGCTTA[A/G]CAGACTGAGGCAGGA | 10580 |
rs137966073 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426040 | ATCTTTTCCTCCAGC[A/T]GTTCTTTATTTGCAA | 10580 |
rs137969979 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349876 | TCTGTTGCTCAGGCT[A/G]GAGTGCAGCGGCATG | 10580 |
rs138028519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486278 | ATTTGTCTGAACTCC[A/G]CGGTTAGAAACTATC | 10580 |
rs138040488 | in-del | -/G | 0.155987 | 0.23165 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323564 | CATTGTAGAGGCCAG[-/G]CCTTCACTTGGAGAG | 10580 |
rs138049794 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523811 | TACCCCTTCCAGAGC[A/G]ATATGATTGTGAGCT | 10580 |
rs138053688 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363568 | TGAAATACATTGAAA[C/T]GAAAGTAATGAGTAG | 10580 |
rs138063398 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535347 | CTTCACTTCCTATAG[C/T]CTACCATCTCTCTCT | 10580 |
rs138069427 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340855 | GCCTTAATGCAATTC[-/T]TTTTTTTTTTTTTGG | 10580 |
rs138109487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343892 | AACTCTCAAGAGGTC[C/T]GTAAAGGGGATATGG | 10580 |
rs138141358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480315 | CCTGGCTCCATGCAC[A/G]CAGAGGAAAAGCTCC | 10580 |
rs138157321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552728 | CAACTTCCACAGACC[A/C]TCTCTCAGAAACTTG | 10580 |
rs138166873 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436587 | ACAAAGATCAAAATG[C/T]CAAATTGTTTGGAAT | 10580 |
rs138170638 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450686 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 10580 |
rs138173675 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359816 | TCTGGCACTGGTAAT[A/C]CCCTCGCAGAGCTGC | 10580 |
rs138177345 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371598 | ATTAGTTGAAGACAT[A/G]AAAACAGAGAATGTA | 10580 |
rs138183078 | in-del | -/AG | 0.375598 | 0.21616 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527127 | TTCAGCTCATATGAA[-/AG]AATTTTAACAATTAG | 10580 |
rs138198334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328746 | CTCTTCCCATCCTCC[C/T]CACCCACCATTTTTC | 10580 |
rs138280900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444729 | AAGTACAAAGCACAC[A/G]GCATTCTTAGGCTGG | 10580 |
rs138282888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395493 | CATTAATTTTTCAAA[C/T]ACCTCTGCCTACCAT | 10580 |
rs138290125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429561 | TTTGTTTCCTCTACT[C/T]AAACCCAGCTTGTTC | 10580 |
rs138300456 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501675 | CAATGTGCTATGATC[A/G]CACCTGTGAACAGCC | 10580 |
rs138320049 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467247 | CTGACATTTAAGACT[A/C]TTTTAAAACATCTCT | 10580 |
rs138345859 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316700 | TAGCTAGTCTGAAAT[A/G]AGCTGTGCTGTAACT | 10580 |
rs138380952 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554719 | CACACACACACACAC[A/G]CGAAAGTTTTATACA | 10580 |
rs138419183 | snp | A/G/T | 0.0158583 | 0.0877198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495974 | CTGTCGCCCAGGCTG[A/G/T]AGTGCAATGGCATGA | 10580 |
rs138427430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385695 | CCAAGGTACCTTTTC[C/T]CCTACTTCCTTCCCT | 10580 |
rs138437289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462742 | CTTTTTTTCTTTGGT[C/T]AGGGAGGGGGCATAT | 10580 |
rs138451685 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373126 | ATTCCCAGGCTCTTT[C/G]TAATAAATCTGCAAA | 10580 |
rs138454732 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419255 | GAATATGCACCAGCC[-/A]AAAAAAAAAACAAAA | 10580 |
rs138458871 | snp | A/G | 0.241914 | 0.249869 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556589 | GAGTCTTGCTATGTC[A/G]CCCAGGCTGGGGTGC | 10580 |
rs138507074 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354627 | GGACAATCTCTGTAT[C/T]TCCCATGCAGCAGTG | 10580 |
rs138520521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391878 | CCTTAGGCTAGGCTT[C/T]GATAGGTTTATTACA | 10580 |
rs138544714 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350390 | AAGCATAAACTCTTA[C/T]GCAAGATACAGCATT | 10580 |
rs138545890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394942 | CTTATGCCTACAATG[A/G]AACTATAAGAATTAA | 10580 |
rs138546930 | in-del | -/CCG/CGC | 0.391954 | 0.205789 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442524 | TGTGGCACCCCCCCC[-/CCG/CGC]CACCCTTACTTATGC | 10580 |
rs138553390 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550720 | TGAAGAAATGAAACA[A/T]ACTTTTGGTCAAATC | 10580 |
rs138562965 | snp | A/G | 0.00216799 | 0.0328526 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414665 | CCACCTCTGCAGATG[A/G]GGGGGAATGAAATCA | 10580 |
rs138563846 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465805 | GTAGCACATATTCCA[C/G]ACTTGTTAGGACAGC | 10580 |
rs138565241 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323932 | GAGCATGATTGCACC[A/G]CTGCACTCCAGCCTG | 10580 |
rs138566646 | in-del | -/AGTCAAC | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470581 | ACCACTAAATCTGCA[-/AGTCAAC]AGTTCATGCTTTCCT | 10580 |
rs138570325 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340365 | GGAGAGAGCCATCTA[C/T]CTTCATTTTTTTTCT | 10580 |
rs138579383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529439 | TCCTGTAGACATACA[A/G]CTGAGGAGATTAGGG | 10580 |
rs138586035 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446125 | CTATGCAGTGTCACA[A/G]CTTGGGTGTGCCAGC | 10580 |
rs138592409 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420550 | GCAAGTCATTTACCG[A/G/T]ACAAGTGACCTCCCC | 10580 |
rs138596885 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345267 | AGAAAATTGAGTGGG[G/T]GAGAAGTTGATAACT | 10580 |
rs138644916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535959 | AGGAAGCTCATTTGC[A/G]GGCACCACTGAATAG | 10580 |
rs138652438 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338955 | TCAGGTGATTCACCC[A/G]CCTCGGCCTCCCAAA | 10580 |
rs138679834 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486756 | TATTATCCTTTTTAA[A/G]TATAATATATAAACA | 10580 |
rs138681144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542541 | CACCTTATCTCGCCA[C/T]ACTCTTTGTGGATTC | 10580 |
rs138694900 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480882 | AGGAGAGGGCAGACA[A/G]CAATCAGAAACAGTT | 10580 |
rs138715986 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523473 | TAAGAGGCAATAGAC[C/T]CCCATTTGGAAACCC | 10580 |
rs138730321 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509165 | CCCTGTACATCACCA[A/T]ATATGAACAGAAGCC | 10580 |
rs138735824 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474345 | CTACAAAGCATGCGA[A/G]GCATCTTGCCTTGCC | 10580 |
rs138739784 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395271 | AGACACATAGAAAGA[C/G]ACAATACCATTACTC | 10580 |
rs138773057 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336588 | TGCCGCTCTGTCTGC[C/T]CAGCCTCACTTCCTG | 10580 |
rs138783346 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523963 | CATATAATTTCTTTC[A/G]TGCATATTTAACTGA | 10580 |
rs138789105 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313993 | TACTCAGATTCACAA[A/C]CCTGGTTACTACCGT | 10580 |
rs138845299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436845 | TTGAACCCATGCCTT[A/G]TCACTCCAGCTTCAG | 10580 |
rs138850186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326654 | CCATTACTATCTATC[A/T]CAAGAATTAGCCCTT | 10580 |
rs138868870 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371233 | CCAGCATCACCATCC[A/G]TCACCTCAACTACAT | 10580 |
rs138869588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363062 | TATCTATACTGATAT[C/T]GTTATTCACATTTTA | 10580 |
rs138895335 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409433 | AGAACCCAGATTCAT[A/G]GGTGAAAATTAATAC | 10580 |
rs138907549 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470250 | TGCTTTCCACGGGAA[C/G]AGCATTCCAAGTGGA | 10580 |
rs138929900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354824 | GATGTCAAGAATCTG[C/T]ACTTGCTTCATACAT | 10580 |
rs138931236 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413056 | CTGATTTCTGCATGA[C/G]TGGCTTCAGCTTAAC | 10580 |
rs138954517 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552124 | GGCACACACCGGCTG[A/G]ACGCAGTGGCTCACA | 10580 |
rs138973298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500409 | GCAGGGTAGGACATA[A/C]GTCTCCAGCCACTAG | 10580 |
rs138975797 | snp | C/G | 0.000675703 | 0.0183683 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434640 | TAGGGAGAACTAGGC[C/G]TGAGGCGTTTTTCAC | 10580 |
rs138978926 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421117 | GGCTTCAGTGGGCTA[C/T]GATGACACCATTGCA | 10580 |
rs139023344 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471161 | ACCACTGTGCCCCCA[A/G]TTCTGATTTTGCAAA | 10580 |
rs139026053 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321217 | CACTCTGTTGCCAGA[C/G]TTATCTCCCTAAAAC | 10580 |
rs139039987 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547670 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 10580 |
rs139048995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476395 | CTTTCAACTCCCGAG[A/G]TAGGTTTGGCCCAAT | 10580 |
rs139053276 | snp | A/C/G | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559665 | TGCCAACAGACCAAC[A/C/G]CTTCCCTTCTTTCCC | 10580 |
rs139063731 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426817 | TGTGAGTCCCTCCAG[C/G]ATTGTACCAAACCTG | 10580 |
rs139066674 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558356 | GATCTACAATCTATC[A/C]CCCCGAGTTCCCACC | 10580 |
rs139106989 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562869 | CCAGCCCACGGCCTT[C/T]CCCTATCTGCACCTC | 10580 |
rs139115529 | snp | C/T | 0.000439464 | 0.0148168 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434693 | ACAGCAGAAATAGAG[C/T]GTGCGCGTAAAGGGT | 10580 |
rs139151612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556900 | AAATTTTAATGGCAA[C/T]AGATTAAAAGAAACT | 10580 |
rs139157795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471869 | TCACCTACTCTCTCC[C/T]GTTATCCTCATAAAG | 10580 |
rs139180122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357177 | TAAAAAGAAAAAGGA[A/G]AGGTAACATGCTCAT | 10580 |
rs139214262 | in-del | -/CGAAAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430463 | CTCAAAAAAAGAAAA[-/CGAAAC]AGAAAAAAAAACAAA | 10580 |
rs139282648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391537 | CCTCCCTTCTGCTAA[C/T]ATCTCTTCCATCCCG | 10580 |
rs139284161 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427366 | ACCAACATGGCCAAC[A/G]CTCAGACCTGGTGTG | 10580 |
rs139288533 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352332 | CTGATACTAAACAAT[C/T]TTACTTTCCTGGGAT | 10580 |
rs139296163 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389188 | GCTTTACCCCCCACA[C/T]TTAGGAAGAGAAAGG | 10580 |
rs139298119 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438103 | ATCCTGAAGACCCAG[A/G]CCTCCAGAACTAGGA | 10580 |
rs139312521 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430122 | AAATTTGTAAGACAC[A/G]AAAGTATTCTGGGAC | 10580 |
rs139335865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392707 | TGCATGCCAAAAATC[A/G]GACGTGATCGTCAGC | 10580 |
rs139337434 | snp | A/G | 9.21718e-05 | 0.00678804 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337216 | CAGAGGTGACAGCGT[A/G]CATCTCGGGGGACAG | 10580 |
rs139341935 | in-del | -/ACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432329 | CACACACACACACAC[-/ACA]CACCCCCCCCCCCCA | 10580 |
rs139347563 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488490 | TGTCAAAAATCCTAC[A/G]CATCTCTTCCTTTCT | 10580 |
rs139357424 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379349 | CACACCACTGTACTC[C/T]AGCCTGGGTGATAGA | 10580 |
rs139389721 | snp | C/T | 0.000805639 | 0.0200542 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422771 | CAAAATCTAATCACC[C/T]TTCCTGAGTGTTCAT | 10580 |
rs139408157 | in-del | -/TGTTT | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382682 | ATTGGTCTATATGTC[-/TGTTT]TTATGCTAGTACCAA | 10580 |
rs139417499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319217 | TCCAATTGCCTCACT[A/G]TTTAGCAAAACTATC | 10580 |
rs139443140 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329285 | GGTGTGATCATGGCT[A/C]ACTGTAGCCTTGACC | 10580 |
rs139450195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364741 | ACAGACGTGAGCCAC[C/T]ACGCCAGGTCTAAAT | 10580 |
rs139453367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481757 | ATTAGAGCTACTCCA[C/T]ATGTGTTGGTTGAAT | 10580 |
rs139460253 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516050 | CACGATAGCCCTGAA[G/T]TGACATCCACACCCA | 10580 |
rs139463744 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554717 | CACACACACACACAC[A/G]CGCGAAAGTTTTATA | 10580 |
rs139472985 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438668 | TTCCTTCTGTGACTG[C/T]AGGCCTTGCTCCAGG | 10580 |
rs139488996 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493277 | CCTGGGCGACAGAGT[A/G]AGACTCCGTCTCAAA | 10580 |
rs139491881 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367463 | TTTGGAAGAGGAGGA[A/C]AGAACAGAAGAAAAA | 10580 |
rs139511091 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439175 | GCGGCATAATATTCC[A/G]TCAAGTAAATACACA | 10580 |
rs139511212 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487305 | TAGAAGCAAGTCAGC[A/G]CTGCCCATGCCCACG | 10580 |
rs139581392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431671 | ATTATCAACCCCATT[C/T]TACAGTTCATCAGGG | 10580 |
rs139660038 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335006 | GGGATGGACTGCTTC[C/T]ACTCCTGCTTAGCAT | 10580 |
rs139668855 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544805 | GCTTCAGGTGAGTAT[A/T]TAAATAGCCCGTGCC | 10580 |
rs139675745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504174 | GCAGATGAGCGCACA[A/G]GGTCTGAATGACTCC | 10580 |
rs139683154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456562 | CCCAGTCTGTGGTAT[G/T]CTGTTATGCAGCAAG | 10580 |
rs139683255 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406695 | CTTAGTCACTATAGT[A/C]ATCTGGCTTGTCCGG | 10580 |
rs139697003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330233 | GTCTCTAAATATTCT[C/T]TTTAATTCAAAAATT | 10580 |
rs139719151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410900 | AAGAAATGCAATCAA[C/T]GAGATACATCGTATC | 10580 |
rs139724483 | in-del | -/AAAC | 0.0513262 | 0.151752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542591 | AGCCCTGGGACTTGA[-/AAAC]AAACAAAGAAAAGAA | 10580 |
rs139732543 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453040 | CCTATAATCCCAGCA[A/C]TATGAGAGGCCAAGG | 10580 |
rs139737147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388822 | TGTCCTTGGTAGCTC[A/G]ATTTGGGGACAGCCA | 10580 |
rs139780934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537684 | GTCCCACAACTATGA[C/T]TCTCATTCCACCCTG | 10580 |
rs139781417 | in-del | -/AA | 0.213937 | 0.247385 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545684 | TGAAACTCCATCTTG[-/AA]AAAAAAAAAAAAGGG | 10580 |
rs139797463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324686 | CACCCTCCACTCACT[C/G]CCTCTGGATTAAGGT | 10580 |
rs139801878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516918 | GCATTTTCCCATGGA[C/T]GTGACATGGAGATAG | 10580 |
rs139817564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520934 | TTACTCTCTGTGAAA[C/T]TTGCTAAAATGGACA | 10580 |
rs139825940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497526 | TCTGACTTTTTATGA[C/T]GTCAAGACCCTCAAG | 10580 |
rs139859986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532033 | ATAAATGCAGTCATG[A/G]AGGAGAAATCAGAAA | 10580 |
rs139865152 | snp | C/T | 0.000267023 | 0.0115516 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383974 | TGAATGAGAGACAAG[C/T]GGGCACTTACCTTTC | 10580 |
rs139885781 | snp | A/G | 9.92539e-05 | 0.00704394 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95375995 | CCAAACTCCAATTCC[A/G]AAAAGAATTTATACC | 10580 |
rs139905546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387251 | CCAAAGGGTCCACAG[A/G]TTCTGATATGTGGAT | 10580 |
rs139906235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402078 | ATCACAGACATGCCA[C/T]ACTCAGGGTCAAGGC | 10580 |
rs139916720 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352877 | TGTTTCTGTAGCCAC[A/G]GGAATGGAGTGATGC | 10580 |
rs139930453 | in-del | -/AAAT/AATA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318030 | CTGTCTCAATAAATA[-/AAAT/AATA]AATAAATAAATAAAT | 10580 |
rs139936125 | snp | C/T | 0.000121161 | 0.0077824 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356360 | AAGTAGGGACTCGGC[C/T]GAGCGGGCTGAGGTC | 10580 |
rs139938686 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463480 | CACATTGTTCACTCT[A/G]ACCCTTTCACAGCAC | 10580 |
rs139941727 | in-del | -/C | 0.103794 | 0.20279 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477077 | TTTGGCGGCCTGAGT[-/C]CCCCCCGGGACAAAC | 10580 |
rs139950285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393325 | GACCAAAAATGGCCT[A/G]TGGTATTTTAACTGT | 10580 |
rs139996432 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472943 | AGGCTGAGGCGGAGA[A/G]TTGCTTGAACCTGGG | 10580 |
rs140008861 | snp | A/C/G | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538408 | CCTGGAAGAGGGAGC[A/C/G]GAAAGCAACAGCAGT | 10580 |
rs140027640 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544870 | TGTAATGCAGGCTGG[C/T]GGCTGCAGACCCTCC | 10580 |
rs140029009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459923 | CGTTGGGGTTGCCTC[A/G]GAACTGCAAAACCAA | 10580 |
rs140030911 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510661 | ACAGGTAGGTATGTC[A/T]GGTTGTCAAAAGTTT | 10580 |
rs140082081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349528 | TGGAGTGATGTGTTC[A/G]TAGCTCATTGCAGTC | 10580 |
rs140095003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525798 | CAGGTATATCTGTAG[A/G]ACAGATTCCACAAAG | 10580 |
rs140101846 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442916 | ACATTTTTAACAATA[C/T]TGAGTCTTCCAGTTC | 10580 |
rs140103802 | snp | C/T | 6.58903e-05 | 0.00573941 | missense | SORBS1 | GRCh38.p7 | 10:95399081 | GTGCTCTTCACCACC[C/T]GCCTACTGTCATCCT | 10580 |
rs140123087 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496416 | GTGCTCAATGATGAG[A/G]TCGCTCCCACTTCCC | 10580 |
rs140125985 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416443 | GGCTGAGCCCAGCCC[A/G]TAGCAGGCCACATGC | 10580 |
rs140126113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369358 | AGGGCTTCAACCATC[A/G]CCTCTCCTCAGGTGA | 10580 |
rs140145714 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373836 | TAATAAGCCCACCAT[G/T]AGGATGCCTCAGACC | 10580 |
rs140146188 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390867 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAG | 10580 |
rs140157260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347044 | CAGCCTCTGCCCCTT[C/T]TCCACTTCCTGATCA | 10580 |
rs140160226 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411157 | AGAGCTGGTTTAATT[A/G]GGAAAAATCAGGGAA | 10580 |
rs140223275 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425787 | CTCATCTTCTGAACT[G/T]GGAAGGTTGGTAGCA | 10580 |
rs140233091 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499844 | ACTATGTCAGCAAAT[A/G]AACTTTAAAATCAAA | 10580 |
rs140238443 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511888 | CCTCCAGCCCTCTAA[G/T]AAGGGCCTTCTCCTT | 10580 |
rs140238974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469882 | AAAGGGCAGACTGCT[A/G]AGCTCTGGCCCCAGA | 10580 |
rs140242794 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428940 | TCCAGACTGGGCTTG[A/G]CTGTCTGCAAATACT | 10580 |
rs140244552 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382794 | TTTCATGCAAGGCTG[A/T]AAACTTCTTGAAGGC | 10580 |
rs140244867 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390665 | TTTTTTTGAGACAGA[A/G]ACTCACTCTGTTGCC | 10580 |
rs140250857 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324652 | TGGGAGCCGACCTTG[-/A]TATGGCTCCAACACC | 10580 |
rs140257071 | in-del | -/AACT | 0.32955 | 0.237006 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535419 | AACCAAGGGAAAGGC[-/AACT]AACTATCAGTCTCTA | 10580 |
rs140259815 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534600 | CAGCAAAGAACATCT[C/T]ACCTGCTCTTTTTGA | 10580 |
rs140273689 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450373 | GGGCTAATTACCTGA[C/T]CACATACCCACTGTG | 10580 |
rs140280033 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419001 | CAGGAGGTCAAGGCT[A/G]CAGTAAGCTGTGATG | 10580 |
rs140286382 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550951 | CTAAACAAGTGCCCA[A/G]CTCATGGCACAGAAC | 10580 |
rs140290065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401313 | GGAGTTCGAAGCTAC[A/G]GTAAGCCATGATCAT | 10580 |
rs140326372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406059 | AATATCGGGCGGTGA[C/T]CGGAAGACGGTTTCA | 10580 |
rs140354948 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397438 | AAAACTTTTTAGAAA[A/C/G]AGAAAAACCAAGAGT | 10580 |
rs140370252 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384960 | GACCCATCGTCAAAC[A/G]GCTTCCTCTGCAAAG | 10580 |
rs140410872 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549624 | AGCTAAATCAATATC[C/T]CTAAAATTTCTAGTT | 10580 |
rs140423080 | in-del | -/GTGGGGGCGGTGGGGGGG | 0.135825 | 0.222405 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433012 | CTGGCAACTACGGAA[-/GTGGGGGCGGTGGGGGGG]GTGGGGGCGGGTGGT | 10580 |
rs140431698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528105 | CAGAACACTATGCAA[C/G]ACCCTTGGAGAATAC | 10580 |
rs140439615 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412056 | ACAAAAGTGCCTCAC[C/T]TTGATTCCTCCATTT | 10580 |
rs140451773 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530941 | CTTTTCAGGCAAAGA[C/T]GGTTTCTCTTTGAGA | 10580 |
rs140453415 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398666 | AGGAATTTCTCAACA[G/T]GCTCCACACAGAACA | 10580 |
rs140473532 | in-del | -/AC/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382996 | TGGTGCTTTTAAAAA[-/AC/C]CAGCCATTAATTTGT | 10580 |
rs140484382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322175 | GGTGGCCCCGAGATA[C/T]CCAGAAACCCCAATA | 10580 |
rs140486084 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444056 | ATAAATAATTTTCAT[A/G]AGCAATTGTATTAAG | 10580 |
rs140496679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366176 | AACAAGACACAGATG[C/T]GATGGTGACAAAATA | 10580 |
rs140508648 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520481 | ACTAAAAATACAAAA[A/C]TTAGCCGGGCATGGT | 10580 |
rs140517307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548960 | TACTCTCAGTTGCCC[C/T]ACCTCACCTCAGGGA | 10580 |
rs140523814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465102 | AAATGGTAAGGAGAA[C/T]GTCATGCTAGTGTCA | 10580 |
rs140524757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448449 | AAAAACTCCGCAGGG[C/T]TCCTATACACTCAGA | 10580 |
rs140552976 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559066 | CATGCCTTTCTCCTA[G/T]AGACAGGTCAAATCC | 10580 |
rs140578892 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359360 | CATTGAGCACTACAC[A/G]GATAGTATTCTCTCT | 10580 |
rs140665126 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507663 | ACGCCTGTAATTGCA[A/G]CACTTTGGGAGGTCA | 10580 |
rs140703392 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423504 | TCCGCTCACAGCCAC[A/T]GTTTGCCAATCCCTA | 10580 |
rs140713063 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347931 | AGATAGGGTCCCACA[A/G]TGTTGCCCAGGCTGG | 10580 |
rs140713195 | in-del | -/TTTTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449156 | TTATTTTCATCTACT[-/TTTTA]TTTTATTTTATTTTA | 10580 |
rs140749666 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350900 | CACAGGCAACACAGT[A/C]GCATGATAAAATGCA | 10580 |
rs140753175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354233 | AGAAAAGGGGCTCTT[C/T]CTCAGGCCCTGACAG | 10580 |
rs140763690 | snp | A/G | 5.1499e-05 | 0.00507414 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336563 | CCTCCCCGCCTGCTC[A/G]CCACCTCTATGCCGC | 10580 |
rs140768912 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417764 | GTAGCTGGGACAAGC[A/C]CATGTCACCACACCC | 10580 |
rs140786057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385150 | CCTTGTGGAAGTGGC[C/T]GTATCTTCTGAACTA | 10580 |
rs140788667 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520340 | AAAAAAAAAAAAAAA[-/AA]GCTTCTAGGCCAGGC | 10580 |
rs140791641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547170 | AGACACCTGACCTCA[G/T]ATACATCACTGGCCT | 10580 |
rs140802281 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429457 | TGAGCCACTGCGCCC[A/G]GCTTACTGACATCCT | 10580 |
rs140813414 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490496 | GACTGGCAGATGAAG[C/G]TGTCTGTGAACATCA | 10580 |
rs140815475 | snp | A/C/G | 3.29491e-05 | 0.00405877 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351302 | GTGCGTCGGAATGAC[A/C/G]CCTGTGTGGCGTCGA | 10580 |
rs140816451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469122 | GCCAGGCCTCCAAAA[C/T]GCTCAGTAAATGACA | 10580 |
rs140822548 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390412 | TTCTTGACATCAAAT[A/G]TGCCAAGTGAGCCAA | 10580 |
rs140857664 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425104 | GCTATTTCTAGTCCA[C/G]CTTTGTCAAATAAGT | 10580 |
rs140865650 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553167 | GCAATGAGCTACAAT[C/T]GCACCTCTGCACTCT | 10580 |
rs140879014 | snp | C/T | 5.01693e-05 | 0.00500821 | missense | SORBS1 | GRCh38.p7 | 10:95339282 | CCGGGATCCTCCCTT[C/T]GTACCAGTTCTCATC | 10580 |
rs140920974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331327 | CAGAGAAAAAACACA[C/G]CTAAAAACATGGGCA | 10580 |
rs140931317 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376631 | GCACATGAGTAGGTA[A/G]GAAACCATGTCCCGT | 10580 |
rs140935137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482613 | ATTTAGTTCTTCTTT[C/T]GTGTTTATTACTGGC | 10580 |
rs140938703 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522693 | GGTACCTGTTTATAG[A/G]TCAGGCATTAAGCTG | 10580 |
rs140940725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439739 | AGCTCATAACAGTAA[A/G]AGCCCAAAGATGAAG | 10580 |
rs140945717 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512287 | GCCAGGCATGGTGGC[A/G]CATACATGTAGTCCC | 10580 |
rs140979495 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554139 | TCGCTGCAACTTCCG[C/T]CTCCCTGGTTCAAGT | 10580 |
rs141000980 | snp | C/T | 3.29679e-05 | 0.00405991 | missense | SORBS1 | GRCh38.p7 | 10:95318370 | TCAACGATATCTCCA[C/T]CGCGGAGTTCCAACT | 10580 |
rs141045287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518086 | GCAAGGTATGGAAAA[C/T]AATGCTGCCAGCTGC | 10580 |
rs141064029 | snp | C/T | 7.18559e-05 | 0.00599356 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337096 | CCCTTGGTGACAAGG[C/T]GAGGTGGTCAGTGTT | 10580 |
rs141072154 | in-del | -/TC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506058 | ATTTATTGCTGCCAA[-/TC]TCTCTCTCTCTCTGT | 10580 |
rs141072760 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348404 | GCAGCACAGCATTCA[A/C]ACTTTGGTAACTGAG | 10580 |
rs141103710 | in-del | -/AG | 0.0670745 | 0.170406 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433348 | CAGGTCAACTTTTAG[-/AG]TTTCCTTGAGAAAGA | 10580 |
rs141110378 | in-del | -/ACACAC | 0.455977 | 0.141681 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432313 | AGGGGACCGTAAGAG[-/ACACAC]ACACACACACACACA | 10580 |
rs141120672 | snp | A/G | 0.0150606 | 0.0854603 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313295 | TCTGGTGGGGGATGG[A/G]AAGCTGATGGGATCC | 10580 |
rs141124490 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394949 | CTACAATGGAACTAT[A/T]AGAATTAATTTAAAG | 10580 |
rs141129911 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546715 | ACTGTACCATAGGTG[A/T]AGCCTCAAGCACTCA | 10580 |
rs141137129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455330 | CCACTTTCTCCTCAC[A/G]TGGTTTCTCTGAGTA | 10580 |
rs141140429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378976 | GTGCCAGGTTTGGTC[A/G]CTCAAGCCTGTAGTC | 10580 |
rs141140639 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333534 | CTGTAATCCGAGGAG[A/G]CCGAGGCGGGAGGAT | 10580 |
rs141152421 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441712 | GACACAGACAGGTGA[A/G]GCTGTGTGCTTGCTG | 10580 |
rs141187877 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362219 | GTGCTAACGGGCAGG[C/T]TCCGGAGGCAGTGGA | 10580 |
rs141230178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489418 | TGCTCACAATACTTA[A/G]TGAACACCCATCAGG | 10580 |
rs141238501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407033 | TAAAGCAGCCACATA[A/G]ATAAAAATAGAACAT | 10580 |
rs141238577 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362666 | ACTCTCCACCTCCCG[A/C]CTTATCATTGCTCAC | 10580 |
rs141247354 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328434 | AACACATTAACTTTG[G/T]TGTAATTTGAATCTG | 10580 |
rs141296230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529301 | GAATATCAAAAACAG[C/G]CTGCAGAAACAGTTC | 10580 |
rs141305760 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499023 | AGGGCACACAGGATC[A/C]CTCTGTACCATTTGT | 10580 |
rs141354228 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377116 | ATGACTAATTAAGTA[C/T]GTATATATGTTTCAA | 10580 |
rs141382089 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365607 | TAGAGCTGAAGGCCC[A/G]GCTCAATTGGAAGCT | 10580 |
rs141399089 | snp | C/T | 6.60012e-05 | 0.00574423 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395004 | AGTTTATGGTACCTT[C/T]GGAAGTTTGCTGGAT | 10580 |
rs141418156 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495964 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 10580 |
rs141457960 | in-del | -/A | 0.323671 | 0.238899 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550653 | TTTCAATCATTTAAC[-/A]AACACTTCTTGAGAA | 10580 |
rs141467872 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520354 | AAAGCTTCTAGGCCA[G/T]GCATGGTGGCTCAGG | 10580 |
rs141480742 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495616 | TAAAATTTTAAGGGG[C/T]CTTTGTTTGATGGCT | 10580 |
rs141485449 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471704 | CCAGCCTGGGTGACA[C/G]AGCAAGATCCTGTGT | 10580 |
rs141487849 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413311 | GACGATTTAAACAAG[A/C/G/T]CTCCCTGACCCTCAG | 10580 |
rs141490246 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392380 | TGAATACATCAGTGA[C/T]CTATGCCCGGATATG | 10580 |
rs141499857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536867 | ATAGTCACATTGGGA[C/T]GAAGCACCCTGGGAA | 10580 |
rs141501988 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559874 | GTAGATATGTCCATC[A/T]TCTGTCTTCTGTCAT | 10580 |
rs141508046 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421313 | ACATGGTCTATTCCC[A/G]TCATCAAAATGACAA | 10580 |
rs141511991 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345610 | GGACAATGGGGTGGC[A/C]ACTGACCATTGTACT | 10580 |
rs141551430 | in-del | -/C | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441192 | TGCTCTGTAGAAAAA[-/C]AAACACCACACAATG | 10580 |
rs141562230 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560447 | CATGGGGATGCAGAA[-/T]TCGACAGCACATTCC | 10580 |
rs141592065 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552274 | GGGCGTGGTGGCATG[C/T]GCCTGTAATCCCAGA | 10580 |
rs141611530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495960 | AACAGAGTCTCACTC[C/T]GTCGCCCAGGCTGGA | 10580 |
rs141615867 | snp | A/G | 5.64924e-05 | 0.00531441 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414467 | ACATTCAGAAAAGCC[A/G]TGAGGAGGGGAGTCC | 10580 |
rs141657502 | snp | A/G | 0.00052707 | 0.0162252 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95410691 | TGTGGAGGGATAGGC[A/G]GATGAAGGCTTGCTA | 10580 |
rs141668580 | in-del | -/CA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408591 | AAAGGGGGGGGGGGG[-/CA]GGGAGGGAGGCATTT | 10580 |
rs141684921 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420936 | CACCTTCACAGAAGG[A/C]AGGCACAGGGAAGCG | 10580 |
rs141710953 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480934 | TAACACTTGAGGTAG[A/G]AGGTAATTAGGCCAA | 10580 |
rs141722522 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312046 | ACGACTGCAGATAAA[A/T]AGGACTGCAAAAACC | 10580 |
rs141728286 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439621 | CTACTGGCAGTACCC[A/G]AGCCTGCTTAGAGGG | 10580 |
rs141732244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391552 | CATCTCTTCCATCCC[A/G]TAGACAGCAGTCTCC | 10580 |
rs141753144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437797 | GATGTCATGTCCTCT[A/G]TGTTGGCTGAGACTT | 10580 |
rs141761129 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360125 | CCTTTTCTAAATTTC[C/G]TATTCATTATCCACC | 10580 |
rs141770318 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394452 | ATCTGGATAGACTCC[A/G]GTGATACAGTCAGCA | 10580 |
rs141786528 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481440 | AATCTCATGCTTAGT[C/G]GATGATTCCTACCTC | 10580 |
rs141787982 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429000 | GGCCCAGGGGCTCCT[-/A]AGGCCCCAGGATAGG | 10580 |
rs141831790 | in-del | -/A | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514135 | GAAACATCTGAGGGG[-/A]AAAAAATACATCCTC | 10580 |
rs141876627 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561924 | TTGCTGTTGTCATTC[A/G]TGTGCTCTGTACCAG | 10580 |
rs141882725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476160 | AGGGCAAAGTCCCAG[C/G]CTCAAACAGCAGGTG | 10580 |
rs141886579 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561159 | TGGGGGGATGCTCTG[G/T]GGGAGGGGGTCCCCC | 10580 |
rs141891382 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475417 | GAACTCCATTTTTCC[C/G]CCTCAAATACGAAAC | 10580 |
rs141892210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519242 | GAGCTGGAGCCAAGG[C/T]GCCTGGTGCTGGCCA | 10580 |
rs141906051 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435622 | AAGAGGGATGGGAGC[C/T]CTGTGTGAAGGTGCC | 10580 |
rs141915650 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323333 | GGTAATATATGAAGT[A/G]CCAACCAAGACCATT | 10580 |
rs141924369 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492819 | CCTGCCTGATGCCAC[A/G]TGACCCAACATCTGC | 10580 |
rs141933545 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383582 | CTTCTTTTTAAGTTA[A/T]AGTCATTGCTATGAA | 10580 |
rs142007836 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556347 | AACACATACACATTC[A/T]AAAAAGACTGAATTC | 10580 |
rs142009225 | snp | C/T | 0.000131822 | 0.00811748 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95432542 | CCGGAGAGTCACCGC[C/T]CCCTTCCCAGTGCAG | 10580 |
rs142028708 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426663 | GTCCTGACTCTCCAC[A/G]CAGAGTAGGCAACAG | 10580 |
rs142091015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325169 | ATGCCAAGACCGGTG[A/G]TCTGGGTCACACCTC | 10580 |
rs142105763 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500968 | AACACCTGCACACTG[C/T]CGGCCCTTCTTCCTT | 10580 |
rs142109598 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483089 | GTTCAGTTATTCAAG[-/T]TTTAGGTTGGTTGGG | 10580 |
rs142114184 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447513 | ACTTGATTTTATATA[C/G/T]GTACAGCTACTTCCA | 10580 |
rs142125597 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516979 | TGTCTCTGAGAGGGA[A/G]AGGCAGAGGACACAA | 10580 |
rs142127658 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433110 | GCAAATCTCCTTGGA[A/T]CAGCAAGTCAAGACT | 10580 |
rs142143567 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338672 | AAAAGGCCATTTGTA[C/G/T]GCATAAAGACAAAGT | 10580 |
rs142143931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465258 | AAGAGGCCAGGCGTG[A/G]TGGCTCATGCCTATA | 10580 |
rs142144391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455917 | CTCCAGCATGGGTAG[C/G]AGAATGAGACCCTGT | 10580 |
rs142147523 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409262 | TTTTTTTTAAATATG[A/G]GTCACAAGGAAGTTC | 10580 |
rs142149824 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460523 | TTGCGACCAGCCTGG[G/T]CAACATGGTGAAACC | 10580 |
rs142149961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384837 | ACACATCATTAACAA[A/C]GAAGTTCTGCAGCTA | 10580 |
rs142169359 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342234 | AGAAAGGTTCTGAAG[C/T]TAGGCAGATCTGGTC | 10580 |
rs142186220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412906 | GTCACATTGGGCCTG[C/G]TGCTGACCTAACTAC | 10580 |
rs142194162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318990 | AGGTGGTAGTGCCTG[C/G]GGATCGGGGACCCCT | 10580 |
rs142205218 | in-del | -/TGCCCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448269 | CCAACTACATGCTCA[-/TGCCCT]CTTCTTTAGAACCAG | 10580 |
rs142230661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511674 | GCCTGGAGAAGCCAG[C/T]ATAGACATGGAAGAG | 10580 |
rs142240284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396403 | TTCTCCTTTAGACCT[A/G]TGACATTCTCCGGAG | 10580 |
rs142247060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544871 | GTAATGCAGGCTGGC[A/G]GCTGCAGACCCTCCT | 10580 |
rs142252231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459792 | CAAAGAAAATAAATT[C/G]AGTGCGTGAGAGCTC | 10580 |
rs142272069 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496439 | CACTTCCCAAACACC[A/T]CTTGGCTGTGTTCCC | 10580 |
rs142308190 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539576 | CTACATTGTACTAAT[G/T]CCATGACTTTAAATA | 10580 |
rs142312115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455132 | AGTTAACCTTGCTAA[A/G]CCTCAGTTTCCTCAT | 10580 |
rs142335811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340206 | AGAACAACTTCTCTG[A/C]ACAATGTAATTATGT | 10580 |
rs142392708 | in-del | -/TTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325560 | GCACTACTTCTTTTT[-/TTTT]CTTTTTTTTTTTTTT | 10580 |
rs142392711 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342101 | GCAGGGCATGCCTTC[A/G]TTGCTTTAAATTGCC | 10580 |
rs142405424 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406636 | CTAGTAGTTGGGTAC[A/G]ATTATTCTTTCCCAT | 10580 |
rs142407983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333973 | GAATAAATGATCATA[A/C]CATTTCAGAATATCT | 10580 |
rs142455784 | snp | C/G | 1.79319e-05 | 0.00299427 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337100 | TGGTGACAAGGCGAG[C/G]TGGTCAGTGTTATAG | 10580 |
rs142498173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461538 | AATTTGCATTTCTGG[C/T]AGATGTCATTTAGGG | 10580 |
rs142505632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383324 | GGGAGCCTGAGGCAT[A/G]AGAACTGCTTGAACC | 10580 |
rs142512875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429637 | AATCAAAGGGATTCC[A/G]TTTGTTAGGCTAATT | 10580 |
rs142525367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523838 | AGCTTTGATTATTTC[C/T]CATGTATTTGGCAAA | 10580 |
rs142550228 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434049 | GTACAGAAGGAAGCG[A/G]TGAGCCAGAGCTGAC | 10580 |
rs142561305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487680 | TGGGAAAACTAAGGC[A/G]CCCAACGAGGAGATG | 10580 |
rs142570151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395837 | GCCTCAATATTTAGA[C/G]CACTTCGATATTTAG | 10580 |
rs142580596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394341 | TGGGTAAAGGCAGCT[C/T]TGACCAGAGCCCCAC | 10580 |
rs142585308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364841 | CAGTATGGGGCAGAT[A/G]AGAGTTTACTGCCAA | 10580 |
rs142597794 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424704 | CTGAGGGACAACTGT[A/T]GTTGGGAAAGGTACA | 10580 |
rs142658045 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559577 | GCCCTCCAGCTGAGA[A/C]ATGTGCTCTCTGCAA | 10580 |
rs142663230 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473995 | TATGACAGACATCCT[C/G]TATCCATTCCTTAGA | 10580 |
rs142678441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486994 | CATACCTTTTTTATT[A/C]CTGAAATCACTTACT | 10580 |
rs142679555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542936 | CTGCTAAGCAAAATA[C/T]ATACCCTCTTCTGAA | 10580 |
rs142681595 | in-del | -/AC | 0.221439 | 0.248363 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554693 | AGAAACTCTCTGTGT[-/AC]ACACACACACACACA | 10580 |
rs142682632 | snp | C/T | 0.000399281 | 0.0141238 | missense | SORBS1 | GRCh38.p7 | 10:95406127 | ACCTACCTGAAAGGC[C/T]ACTGAGTCGTTTTTG | 10580 |
rs142695907 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438406 | GGGGGGTCGCCTGCT[A/G]TAAACCACACTGACA | 10580 |
rs142699795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491605 | AGCAGTCACCCTTCA[C/T]AGGCAGGCTTGGCCG | 10580 |
rs142703899 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409744 | AATTAAACCTCCACT[A/G]TTATCAGAAATTCAG | 10580 |
rs142706570 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554558 | AGTCCCAGATACTAG[G/T]GAGGCTGAGGCAGGA | 10580 |
rs142737704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360853 | GAATCTCATTCTGTC[A/G]CCCAGGCTGGAGTGC | 10580 |
rs142746481 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359929 | CAGAGCTCCCCCAGG[A/G]CCCTCTTAATTCACT | 10580 |
rs142751632 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497413 | AATTGTTCAGACCTG[G/T]GTATTTCCCAGGAAA | 10580 |
rs142761588 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417459 | AGGCACATGCCACCA[C/T]GCCTGGCTAATTTTT | 10580 |
rs142767488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536382 | TCCACCAGGCCATTT[C/T]AGAGGCTGGGCAGAA | 10580 |
rs142801219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375715 | AGTGGGGGGAGGTCT[A/G]AGACAAGCAATGATT | 10580 |
rs142883473 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548612 | AGGCTTGCACCACCA[C/T]ACCCAGCTAATTTTT | 10580 |
rs142889152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480415 | GCTGTATCCAGGCAC[C/T]AAGCAGACGCAGAGG | 10580 |
rs142912135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547317 | CTTCCTATTTCATAG[C/G]CTGAAATGCACTGTT | 10580 |
rs142926385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463060 | TCATGCCTCATACTA[C/T]AAAGCTGTGCCTTGC | 10580 |
rs142926792 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368713 | AAACCTGTTGGGCTT[C/G]TATGCTTTCATTTCT | 10580 |
rs142944541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367318 | AAAGTGCTGAGATTA[C/G]AGGCATAAGCCACCA | 10580 |
rs142966903 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484305 | AACAGTAAGTCAGGG[G/T]TGACAAAACCAAAAG | 10580 |
rs142972489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340442 | CGTAGTTGGTTTGTG[C/T]CTTTTGGGTTCAAAG | 10580 |
rs143004708 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419787 | GCAGTCTGCATTCTG[C/T]CCAGTTGGCTATAAA | 10580 |
rs143053033 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499421 | AAGCCAAACATTTTA[C/T]AATTTCAAAATGTGG | 10580 |
rs143080901 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544810 | AGGTGAGTATTTAAA[A/T]AGCCCGTGCCTTTAA | 10580 |
rs143083303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550616 | GATGACTAAATGTAC[A/G]CATATCATCCTAGGA | 10580 |
rs143092037 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553950 | GATCTTGAACTCCTG[G/T]CCTTAAGTGATCCGC | 10580 |
rs143097053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457424 | TCCCTACATGCAAAA[C/T]GGGAATAAAAGCAGC | 10580 |
rs143106693 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495284 | AACCCCCCAAAAGAC[A/G/T]TCACAAGAGTTGTCC | 10580 |
rs143116594 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469123 | CCAGGCCTCCAAAAC[A/G]CTCAGTAAATGACAT | 10580 |
rs143119080 | in-del | -/A | 0.0573587 | 0.15934 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389577 | AGTTCTAAAGAATGC[-/A]AAAAAAAAAGACCAG | 10580 |
rs143134585 | snp | A/G | 0.110167 | 0.207236 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556675 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC | 10580 |
rs143154168 | snp | G/T | 1.64993e-05 | 0.00287218 | missense | SORBS1 | GRCh38.p7 | 10:95381783 | CTACTTTCTTATCTG[G/T]GGGTTCCCAGTCATT | 10580 |
rs143182299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378126 | TTGATTTTGCCAAGT[A/G]TAACTCAGCTGTGGA | 10580 |
rs143201108 | snp | C/G | 1.71534e-05 | 0.00292855 | missense | SORBS1 | GRCh38.p7 | 10:95339316 | CTGCCGGAGCAGTGT[C/G]ATCCTCTCACCCTGG | 10580 |
rs143262691 | snp | A/G | 8.29002e-05 | 0.00643764 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95376053 | CTGGGCTTATATCCC[A/G]ACTCTATAGGGGTTG | 10580 |
rs143271418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328043 | CTGACTTGGCTTAAG[A/G]GAGGCAGCACTCTAC | 10580 |
rs143284600 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449905 | AGCAAACAAGATAGA[C/T]GGGTTAATATCCTTA | 10580 |
rs143288515 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371139 | CCAAGCTCAAAAGAA[A/C]ACCAAGCAAAAATGA | 10580 |
rs143298005 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436767 | TTATAGATAAGGGAA[A/C]CCACACCCACAAAGA | 10580 |
rs143314771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515154 | TTCTCAGACCCCTGC[A/C]TCAGAATTTCTGCGA | 10580 |
rs143320366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386497 | AAAAATTAGCCAGGC[A/G]TGGTGGCATGTACCT | 10580 |
rs143341042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432057 | ACAGTGAACCTCTAG[A/G]AAGCAGGGATGAGCT | 10580 |
rs143360381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386681 | AATGAGAAATAGTTC[G/T]TATAAGATGCGGAAA | 10580 |
rs143374509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530318 | ACCTGTTAGTACTTA[C/T]CACACAGCTTTGTAA | 10580 |
rs143384907 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446889 | GGGCTCAATGACTCA[A/C]ACCTAGAATCCCAGC | 10580 |
rs143390011 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443319 | AAAGCAGCCGGGTGT[G/T]GTGGTGGGTGCCTGT | 10580 |
rs143398930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515079 | GGAGTAAAGTGGTAT[C/T]CACTTGTCAGCAGAC | 10580 |
rs143408522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398512 | GGAGGCTTGGCTGGC[A/G]GAATCCATTCTGAGG | 10580 |
rs143419478 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461055 | AATGCAAGTTTTCTT[A/T]TTGATATTGAGAAAG | 10580 |
rs143423971 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400748 | GAATCCCCAAAGTGA[C/T]GCAAAGTAATCCGAG | 10580 |
rs143429732 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353790 | GGATTACAGGCTTGA[G/T]CCACTGCACCTGGCC | 10580 |
rs143467230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546801 | GAGTGCAGTGGCATG[A/T]TCTCTGCTCACTGCA | 10580 |
rs143469921 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558064 | AAGGCCAATGCAGGC[A/G]GATCGCTTGAGTCCA | 10580 |
rs143473985 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472970 | TGGGAGGCGGAGGTT[A/G]CAGTGAGCTGAGATT | 10580 |
rs143503263 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358724 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 10580 |
rs143524621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353021 | CACCTTAGTAAGTCC[A/C]TCAGCCCTGTAGTTT | 10580 |
rs143536471 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367226 | CCTTTTTTTTTTTTG[-/G]GGTAGAGACAGGGTC | 10580 |
rs143540512 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489600 | CTGAATCCCCAGAAC[A/G]GTGCCTTGGCACAGA | 10580 |
rs143548951 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407390 | CTGCTGAGCTCCAGC[C/T]GGCAGAAGTGAATGT | 10580 |
rs143583590 | snp | A/C/G | 0.000347363 | 0.0131742 | missense, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95341567 | AGGCTGCGGTACCTC[A/C/G]ATGTAGGTGCGTGGG | 10580 |
rs143598048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413741 | TTTCTCTAAGCAGTT[A/G]GGCTTTCCCGGCTGT | 10580 |
rs143602313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339509 | AATGGCAGAGGAGCT[A/C]TCTTGATGCTGGGAA | 10580 |
rs143640912 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333174 | GATTAACTGGCAGTC[C/T]GACACCTTTAAAGGC | 10580 |
rs143677446 | snp | A/G | 0.000131893 | 0.00811969 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95432494 | AGGGCTCGCAGGGCT[A/G]CTGCTTGGGGTTTCC | 10580 |
rs143699989 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490010 | CAAATAAAGATGCAT[A/G]GGTTGTTCAGCGTCC | 10580 |
rs143705721 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408855 | CACCTGCTTAGTGAA[C/T]ATATGGTTTTGCTCT | 10580 |
rs143710691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538521 | CCAGTAAAAGCCAAG[G/T]GTCCTGGGGCTCCCC | 10580 |
rs143718308 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474994 | GGGGTTCTGAAATCA[C/G]GTATTGGAATATAGT | 10580 |
rs143725659 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366560 | AAGAGGCTGGTGGCA[C/T]CCCACAAAGGAGTGG | 10580 |
rs143730433 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535592 | AGAAATCTTGGAAGG[A/G]TACGCAAGAAACTGA | 10580 |
rs143740122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426456 | TTATGTGACTTGGGG[C/T]GGGGGCTTTGAGCCA | 10580 |
rs143772130 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373971 | AAAAGAAGCAGTCTC[A/T]TTAGAAGAACTCTGA | 10580 |
rs143779819 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312267 | TCCTTTACCCCCTTC[C/T]ATTCAAATTTTTAAA | 10580 |
rs143786640 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330049 | GTAAAAGACTGGAGG[C/G]TCTTAACCTGGTGAT | 10580 |
rs143802097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467731 | TGAGCATTAAAAGCC[A/G]CCCCAAATTTAAACT | 10580 |
rs143808353 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387668 | TCATCTAGTAGCCCC[A/G]TGACAGAGATGCCTA | 10580 |
rs143824494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555855 | TTCTTTTCCAAAAGG[A/G]TCTGGGTCCTGCTAC | 10580 |
rs143826063 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325918 | ACCCCTTCTAAACTG[C/T]AATCACTCAAATCAG | 10580 |
rs143830856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439649 | GGGGAAAAGGTGCAC[A/G]GCCTCTTCGCACACA | 10580 |
rs143838806 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457899 | ATGTTTCATGAGGCC[-/A]AAGGACTCAGAGCAT | 10580 |
rs143847213 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537553 | TAATATTAAAGAAGC[-/T]TACTTACTTAATCTG | 10580 |
rs143847228 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484446 | AATAGAGCCCAGTAC[C/T]GCTAGATATTCTAGT | 10580 |
rs143909102 | snp | C/T | 6.73628e-05 | 0.00580317 | missense | SORBS1 | GRCh38.p7 | 10:95354949 | TCAGCTGGTATAAAA[C/T]GTCTTGGCGATTCTG | 10580 |
rs143927450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515373 | GATGTCTGGAGTAGG[A/G]TGGAGGCAGCTACTC | 10580 |
rs143935721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492564 | ACCCTCTACGGTAAG[G/T]GTAGTGATCTGAGTA | 10580 |
rs143938696 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369858 | CAGCCCCTAACCCCA[C/T]CCCACCTGCCCCACC | 10580 |
rs143954151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512166 | CTCACGCTCGTAATC[A/G]CAGCACTTTAGGAGG | 10580 |
rs143957314 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563330 | TAAAGATGCTCATAA[C/T]AGGCTGGGAGTGGTG | 10580 |
rs143963269 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368505 | AATAAATCAATGCAA[A/G]GGTTAATTTTAAAGA | 10580 |
rs143965674 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429254 | CAACTTTCACCTCCC[A/G]GGTTCAAGCAATTCT | 10580 |
rs143978885 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354719 | AAGTCCACTAAAAGA[A/G]GCATGATTGAGCCTA | 10580 |
rs144020788 | in-del | -/C | 0.0463947 | 0.145069 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434905 | GGCCAAGACAACAGA[-/C]CCCCTCCCCTCTAAC | 10580 |
rs144032137 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557722 | CCACCCCCCCACCCC[A/C]CATCCTAGGCTACCA | 10580 |
rs144051817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558573 | CCACAGGGAAAGAGA[A/G]CAAATTACAGAAACT | 10580 |
rs144064942 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515010 | ATAGGCTTTCAGGCA[C/T]AGACTCTAAAGAGGA | 10580 |
rs144077014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511299 | AGCCTCAACACCCCA[A/G]GCTCAAGGGATGCTC | 10580 |
rs144117057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486736 | AAGAATAAAAGGGAT[A/G]CTATTATTATCCTTT | 10580 |
rs144145228 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516564 | ATTGAGGCTCAGATA[A/G]ATGAAGTAACTAGCA | 10580 |
rs144147810 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350561 | AAGAACAAATGAAAC[A/G]TCCCTTGGAGAACTC | 10580 |
rs144149081 | snp | A/G | 0.000499027 | 0.0157881 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432585 | TCCATGTCTGAAAAG[A/G]AAAGGTCCAAAATTG | 10580 |
rs144156482 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441558 | TTTGAGAACTTACTG[A/G]TCATACTGAATGCTT | 10580 |
rs144167269 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363661 | CTGTGATGTTAATTA[G/T]AAAAAATATATATAT | 10580 |
rs144168473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389552 | AGCTGGGATTACAGA[A/T]GTGGCAATCAAGTTC | 10580 |
rs144174018 | snp | C/G | 0.0543475 | 0.155628 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361592 | CTGGGACTACAGGTG[C/G]CTGCCACCAAGCCTG | 10580 |
rs144179614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448527 | CCGGAAAGAATATTA[C/T]ATCTAAAACACAGGC | 10580 |
rs144201912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392068 | GGTGCTGATCTGTCT[C/T]GAATGCCTTTCTTTG | 10580 |
rs144244903 | in-del | -/GGGTAACGCAGT | 0.0520825 | 0.152737 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538426 | AAGCAACAGCAGTCA[-/GGGTAACGCAGT]GGCCCCTTTCCTCAG | 10580 |
rs144255195 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503221 | ACACTCACAGTGGCA[A/T]GTGGCAAGAGGTGGT | 10580 |
rs144293741 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477084 | GGCCTGAGTCCCCCC[A/G]GGACAAACCTGAGAG | 10580 |
rs144299220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531744 | AGTTTCCCCACCACA[C/T]AATATAAATAATAAA | 10580 |
rs144305492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397676 | CCCCAACCATTCTAG[A/G]TTATTCAACAGCAAT | 10580 |
rs144342340 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95401688 | CAATGACTCCAGCAT[A/G]CTCAGGTTTTACAAC | 10580 |
rs144344238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358066 | ATGGCTACATTTGTG[C/T]TTTAAAAGAAAAATT | 10580 |
rs144362583 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549232 | GTGGCTAGCATGACC[A/G]AGAAGCTGAATTTTT | 10580 |
rs144369140 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410910 | ATCAATGAGATACAT[C/T]GTATCATTAATTCCA | 10580 |
rs144377740 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457722 | CTTGGGCAGAGAAAA[C/T]TCAACACAAAGCTTG | 10580 |
rs144424579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335824 | GCTAAGTTCATTTCT[C/T]CAAAAAAATTTTCAG | 10580 |
rs144462979 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330740 | GGTCTTAAACTCCTG[G/T]CTTCAAGTGATCTGC | 10580 |
rs144481330 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536496 | CTCAAGTTAGAAAAA[C/T]GCCTGTCCGGGATCC | 10580 |
rs144482517 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329517 | TGGCCAGTTCCCTAC[C/T]GTTAGTGATGAGAGA | 10580 |
rs144485211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452053 | ATCTGCAGTACAGAC[C/T]CATACCATGCTCAGG | 10580 |
rs144489026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537714 | GATGCTGGAAGGGAA[A/G]TGATTCAGTGCTGTG | 10580 |
rs144493480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345449 | ATACCAGATTTGTGC[C/G]TAGGCTCTAGACACT | 10580 |
rs144503230 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453366 | TTTTTGAGATGGAGT[A/C]TTGCTCTGTTGCCCA | 10580 |
rs144504728 | snp | A/G/T | 0.000530359 | 0.0162759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406178 | ACACAGTGTAAGTAA[A/G/T]ATTTATACAGCACAT | 10580 |
rs144524691 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360396 | GCTGCATCCATACTT[C/T]GAGTTCCTATTCTTC | 10580 |
rs144534018 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546329 | AGACTAGGTAATTTA[A/T]AAACAAGAGAGGTTT | 10580 |
rs144541249 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406747 | AAATCAGCAATGGCC[A/G]AGAAACTTCAGATAA | 10580 |
rs144568999 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468819 | GTGCAGGCTGGGGGC[C/T]GGACAGGGCAGAGTG | 10580 |
rs144577895 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344868 | TGAGTTAGGAGGAAG[A/G]AGCCCTCTCTCCGGC | 10580 |
rs144585399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530022 | CTACACCCCAAACAC[C/T]GTCACCTGCACTGCC | 10580 |
rs144585930 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95400234 | GAAACTATTATCACC[-/T]TTTTTTTTTAATAGT | 10580 |
rs144589978 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380548 | ACAGCAGAGAACCTC[C/T]AAAGAAGGGCAGTAG | 10580 |
rs144606041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348720 | AGGACAGAGATAACT[A/G]TATAAGAGGGAGACT | 10580 |
rs144621373 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481323 | CACCCAGCAGGCCTT[A/G]CTTTCAGCTCTTGCT | 10580 |
rs144631376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399761 | ATAACTTATGCCAAA[A/G]TGTTCAGGAAGCTGT | 10580 |
rs144637454 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474064 | TTCTGAAATGCTTAG[-/A]AAAAAAAAACAAAAA | 10580 |
rs144657727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461738 | GCAGGGAGACAGTTT[C/T]TCCTTTTTTTCCTGC | 10580 |
rs144665923 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383365 | AGGGTGCAGTGAGCC[A/G]AGATCACACCACTGT | 10580 |
rs144694934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465758 | CATCTATGCAGCACC[A/G]CTTTGGGCATTGATG | 10580 |
rs144698509 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547856 | TGCAGCAAAATGGGG[A/C]ACCCCTAAAACACTG | 10580 |
rs144701109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464037 | AAGGCAATTAAGAAT[A/G]TAGGCTCAGGCAGGG | 10580 |
rs144708612 | in-del | -/A | 0.100588 | 0.200439 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484046 | CTGGCCAACATGACG[-/A]AACCCCATCTCTACT | 10580 |
rs144711667 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497642 | CTCTGGATCCATCAT[A/G]CCTAAACCTTTGCTC | 10580 |
rs144715312 | snp | A/G | 0.000181215 | 0.00951706 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336799 | GTCCACTCTCTTCGC[A/G]CCATGGCTGCCTCTT | 10580 |
rs144716045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417946 | TCTAGAAGAAAACCA[C/G]AACTTTCCTCCAAAT | 10580 |
rs144743946 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504090 | GACAAATTAAGGGCA[A/G]TGACTTCCTCTCACT | 10580 |
rs144756120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423835 | TGACTTGCCCAAAGT[A/C]GCACAGCCAGGAAGT | 10580 |
rs144756201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376748 | GAATACAGACAGAAT[A/G]TACTTCGTGTTTTAA | 10580 |
rs144780388 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397735 | ATTTAGAATGCATAC[-/A]TTAAAACATAACTCG | 10580 |
rs144782688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483067 | AAATAGGAATGACTC[A/G]GATTAAGTTCAGTTA | 10580 |
rs144804620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544321 | AGCCAAGCAGAACAG[A/G]TGGGCTCTTGGCCTC | 10580 |
rs144816614 | in-del | -/AGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344859 | TGAAAACACTGAGTT[-/AGG]AGGAAGGAGCCCTCT | 10580 |
rs144820620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529353 | TCTGGACACTTAAAC[G/T]ACCAAGCAGTTTGCC | 10580 |
rs144821024 | snp | C/T | 3.44471e-05 | 0.00414999 | missense | SORBS1 | GRCh38.p7 | 10:95357800 | GAAGTTGGAAGAATA[C/T]ATACTATGAACAGGT | 10580 |
rs144825900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362284 | CAACAAGGAATGTGG[A/T]TCAGTAGAGGCAAAC | 10580 |
rs144829504 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417274 | TGAGATGAGGAAACT[G/T]CATTTTGCTAGATTT | 10580 |
rs144833595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341131 | CAGGCATGAGCCACC[A/G]TGCCCAGCCCTTAAT | 10580 |
rs144858557 | snp | A/T | 1.65773e-05 | 0.00287895 | missense | SORBS1 | GRCh38.p7 | 10:95318424 | CTATATAATGCTTGA[A/T]AGCTAAATCTATACA | 10580 |
rs144874707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425225 | AATTGGGGACACATT[A/C]TTTTGCCCACTTTCT | 10580 |
rs144885653 | in-del | -/AG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357377 | GAGAGAAAGAGAGAA[-/AG]AGAGAGAGAGAGAGA | 10580 |
rs144899180 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520312 | AGAACGAAACTCCAT[C/T]TCAAAAAAAAAAAAA | 10580 |
rs144903641 | snp | A/G | 0.000218673 | 0.0104541 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336577 | CGCCACCTCTATGCC[A/G]CTCTGTCTGCTCAGC | 10580 |
rs144903813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550000 | TCCAAGCAGGGTCTG[C/G]GGATTCTGGCAGAAC | 10580 |
rs144915185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432694 | TGGTTACAGCCATGC[A/G]AAGTCTTTGAACACC | 10580 |
rs144921118 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357297 | AAAAAAATGGCTACC[C/T]TGCTAGAGTTAGGAA | 10580 |
rs144932373 | snp | A/G | 1.6937e-05 | 0.00291002 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95339163 | GGCACTGCGACTTGG[A/G]GAGGAGGAGAAAGGC | 10580 |
rs144949699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362861 | AAGATTCAACAGGCA[A/G]CAGAACGGACAAAAA | 10580 |
rs144950403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476864 | GATCCTGAATCTTTA[A/G]TAATGGAATTAAGGT | 10580 |
rs144987759 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365647 | GGAGTGAGCTGCAAA[G/T]CCAGAGTAGGAGACA | 10580 |
rs145027435 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432734 | TGAAATTAATCTGTG[C/G]GTGGTGGAGAGGGGC | 10580 |
rs145042230 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534308 | AGGGTTTCACTGTGC[A/T]GGCCAAGCCGGTCTC | 10580 |
rs145048416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399393 | TACATATTATTTATG[A/G]GTGCTTTTGCACTAC | 10580 |
rs145052092 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319918 | CTACTGGCCTCCCAA[C/T]ACATGCCCCTTGCCA | 10580 |
rs145060307 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419376 | CTAGAAACAAAACAC[A/G]TGGGCTAGCACGCAC | 10580 |
rs145063959 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484738 | CAGCACTTTGGGAGG[C/T]AGAGGTGGGTGCACA | 10580 |
rs145099153 | in-del | -/CAC | 0.0410537 | 0.137264 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384686 | GTGTACGGTTAAGCT[-/CAC]CGAGTTCAACAGTGT | 10580 |
rs145127594 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439422 | TCCCTTCCTCCTTCT[C/G]TGGCCCTTGATGCCA | 10580 |
rs145132151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551973 | TAAAATTATAAACTT[G/T]CTCCAGGAAGTCCAA | 10580 |
rs145188555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504303 | ACTGCAAAGCATAGA[C/T]ACTTAGAAACCCACA | 10580 |
rs145189062 | in-del | -/AAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528944 | AAAAAAAAAAAAAAA[-/AAAAA]CTGTTTCCACAGTAC | 10580 |
rs145201381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382956 | TAATTATCAAACTCC[A/T]CAGGTAGAGGCCACT | 10580 |
rs145236113 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381073 | GGCCGCTTTTCCAGG[C/G]TGGTCTGCTATATGC | 10580 |
rs145237363 | snp | A/G/T | 0.000547585 | 0.016538 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384205 | ACCACTTTCCCTTCC[A/G/T]CCCCCACAACCAGGT | 10580 |
rs145253738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370532 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTCCTT | 10580 |
rs145332304 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420993 | ATAGTTTTTGAGCAG[C/T]ACAGCTTCCTTTAAG | 10580 |
rs145336818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341849 | TCAGGAAATTACATC[A/G]CATTTGGCATTTTTC | 10580 |
rs145339522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559425 | ATGAAAGCAGGTAGG[A/G]GAAGGAAAAGGCCAA | 10580 |
rs145358044 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347344 | CCCTACTCTTACAGA[A/G]TTGCCTTTATCTCTA | 10580 |
rs145367771 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514242 | ACACATTCAACTAGC[C/G]TTATGAGTCATCTTC | 10580 |
rs145371312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425930 | CCTTAGAGCTCCCAA[A/G]CTGGGGGGAGTGCCT | 10580 |
rs145379525 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321061 | GGCTAGGCTTCTTTA[C/T]ATGTATCTCTGTTGG | 10580 |
rs145389444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489078 | TTCACATCACTCTCC[C/T]TCCCTATGAACACCC | 10580 |
rs145395615 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336457 | AGATGGACCAGGGGC[A/G]AGACGTGCAGCCCAC | 10580 |
rs145414895 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365563 | GGCACATCCTAGGAC[C/G]TAGAGGACCTGTGAC | 10580 |
rs145441813 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510988 | CTGTCTTTGCTTTCT[A/C/T]CTTCTCCCTACAACC | 10580 |
rs145459118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521324 | AACGGCACACAGAGA[A/G]CTTGGAGCTCAGTGC | 10580 |
rs145477029 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505774 | TATAAAAACAAAAGA[C/G]GGCGTCTCTGATGAC | 10580 |
rs145481273 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464644 | CCACGCATAACTCTC[C/T]GAAGGAAGGGCTGAA | 10580 |
rs145483012 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394158 | CCAAAGAGAGATACC[C/G]TGAGGGCCCATGAAA | 10580 |
rs145489487 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384176 | GAGAACAGGGCAATT[A/T]TCTTCCCTCATCCAC | 10580 |
rs145507731 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526419 | ATATAGTTTTGAAAG[C/T]GCCCCCCTCTCTCAG | 10580 |
rs145558403 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385030 | CAAATCAAACTCACG[C/T]GTGTCTCTATGGTGG | 10580 |
rs145589898 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389185 | CTGGCTTTACCCCCC[A/T]CACTTAGGAAGAGAA | 10580 |
rs145604295 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382112 | TCTTTCACCTTGCTT[C/G]GCTCTATGGGCTTTT | 10580 |
rs145616362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398808 | CATTTACTTGACCAC[A/G]AAACCCTTTATTCAT | 10580 |
rs145635811 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327349 | TCCAGAAAGTGCTTT[C/T]TTCTGTATTTGTACA | 10580 |
rs145653133 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554722 | ACACACACACACGCG[A/C]AAGTTTTATACAAAT | 10580 |
rs145655706 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322868 | CATTGGAAAGGATTC[A/G]AAATAAAAGCATGAG | 10580 |
rs145675385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521955 | TAAGCCACCACACCC[A/G]GACTTCCTTCTCTAA | 10580 |
rs145679780 | snp | A/G | 1.6516e-05 | 0.00287362 | missense | SORBS1 | GRCh38.p7 | 10:95315111 | GTACCAAACTGCTTT[A/G]TCCTTCTTGAAGTAC | 10580 |
rs145680168 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523590 | CACATGGTTGTAACC[A/G]TAGCCCATATGCAAT | 10580 |
rs145684096 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440584 | TCTGTCTTCCCTAAC[A/C/T]CACGTTTTCTACCTC | 10580 |
rs145713141 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444199 | CCTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 10580 |
rs145723367 | in-del | -/AATA | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553212 | GCAAGGCCCTATCTC[-/AATA]AATAAATAAATAAAT | 10580 |
rs145726848 | in-del | -/T | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392097 | TGAAAGGCATACATC[-/T]TTCCTATGTTAAGAA | 10580 |
rs145738486 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538590 | TCGAGTTAGATTAAA[A/C/T]AGTAACTGGTAACAG | 10580 |
rs145743730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454063 | TTACCAATACTTACC[C/T]GTACCAAACATCAGG | 10580 |
rs145753770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331580 | TGCACACCTTTCATG[A/G]TCCTACCTCTGGGCC | 10580 |
rs145753897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348180 | GTTTGTGTCTGTAAC[C/T]AAAGGGCATAATTTC | 10580 |
rs145764028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407439 | TGTTGCCAACATGGC[A/G]AAACCCCATTTCTAC | 10580 |
rs145786164 | in-del | -/ACATGCAACCTAG | | | | | GRCh38.p7 | 10:95488756 | TTTTACTCACATGCC[-/ACATGCAACCTAG]AAGGCTCTACCTTCA | 10580 |
rs145808732 | snp | C/T | 0.000131859 | 0.00811862 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95321977 | CAAATCTTGTGAGGT[C/T]TGACTCCTGTCGGGG | 10580 |
rs145811502 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535685 | AAAATGAAAGAGGGT[A/G]TGATTGATCATTCAC | 10580 |
rs145837961 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362521 | ACGTGTCCCAAACCA[C/T]CTTCCATCACACAAC | 10580 |
rs145848357 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532721 | ATCAATCCCAAACCC[A/G]CCCAGTGTCTGGATT | 10580 |
rs145867466 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483584 | AGTGCAATGCAATGG[C/T]GCCATCTCGGCTCAC | 10580 |
rs145871025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354319 | AAGTTCTTGGCTGGG[G/T]TTTTCCAGCATTTCT | 10580 |
rs145972001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334811 | TTTTCAACTAGCCAC[G/T]TCACCATCTCTTCTA | 10580 |
rs145978322 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340239 | TGAATAAGCATGATG[G/T]TGATAATAATAATAC | 10580 |
rs145985349 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395845 | ATTTAGAGCACTTCG[A/C]TATTTAGAAACAGTT | 10580 |
rs146012000 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475803 | CATAATTATCATATG[A/T]ACATTAATATTATAT | 10580 |
rs146018187 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506263 | CATGTGCACACACAT[-/AC]ACACACACACACACA | 10580 |
rs146021723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520924 | CAACAGACTTTTACT[C/T]TCTGTGAAATTTGCT | 10580 |
rs146031304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523903 | AGCAGCAAGACCATG[G/T]CTGATTTCCACTTTT | 10580 |
rs146033309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472767 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10580 |
rs146034715 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393141 | AGACAGAAAGACTGC[A/G]CTCTCTACACCAAAT | 10580 |
rs146088687 | snp | A/C/T | 0.00110565 | 0.0234884 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356019 | CCTCTGGCATCCAGG[A/C/T]GCCACTCAGGCTGTC | 10580 |
rs146091490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333244 | TACCTGTGAGCTTTC[A/T]TCTAAATAACAAGAC | 10580 |
rs146117284 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371992 | GAATTACCTTTCTAT[C/T]CTCTCTAGGAAGGAT | 10580 |
rs146119820 | in-del | -/A | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312974 | ACAACAACAAAAAAA[-/A]AAAAAACAGTGCTCT | 10580 |
rs146125154 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455137 | ACCTTGCTAAGCCTC[A/G]GTTTCCTCATCTATA | 10580 |
rs146136230 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496315 | CTGACTTTGAAAAAG[A/C]CTTCTCTCTTTTCCA | 10580 |
rs146136589 | snp | C/T | 0.00125117 | 0.0249804 | missense | SORBS1 | GRCh38.p7 | 10:95399079 | GAGTGCTCTTCACCA[C/T]CCGCCTACTGTCATC | 10580 |
rs146137624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95416168 | TTGAGGGAGAGGAGG[A/G]CGTGGGGGAGAGAGA | 10580 |
rs146142344 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544816 | GTATTTAAATAGCCC[A/G]TGCCTTTAATAATTA | 10580 |
rs146155044 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493095 | CAGGAGTTTGAGACC[C/T]GCCTGACCAACATGG | 10580 |
rs146157219 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410942 | TTAGAAGTTTAAGCC[A/G]GAATGCTTATCCTCT | 10580 |
rs146180644 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458053 | CAGGGCTGGAAAAAA[-/AC]ACAGTTTCCAAATGT | 10580 |
rs146207413 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409308 | CACTTTGTCCCACAT[C/T]ACAGACACTTTCTGG | 10580 |
rs146209691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373513 | TTTGGGTGGCTAAAG[C/T]GAAGGGGTGGAGGAA | 10580 |
rs146220720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378989 | TCGCTCAAGCCTGTA[C/G]TCCCAGCAGTTTGGG | 10580 |
rs146240906 | in-del | -/TCTC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479969 | CCCACTCTCTCTCTC[-/TCTC]TCTCTCTCTCTCTCT | 10580 |
rs146257443 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437997 | GTTAACCAAGCTACA[A/G]ACATAATCATGACTA | 10580 |
rs146263506 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562558 | AGATAAGACACTCGC[C/T]CTTTGGGCTGAGCAC | 10580 |
rs146265011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476274 | TACTCAATTTCCAGG[A/G]CAAAAACGTCCTACA | 10580 |
rs146323650 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314052 | GTAGATCTGGAGCCA[C/T]GGCAAACCCTGGGCA | 10580 |
rs146339658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395473 | CATTCAGCAAACAAG[C/T]AGATCATTAATTTTT | 10580 |
rs146349341 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379285 | CTTGGGAGGCTGAGG[C/T]GAGAGGACTGCCTGA | 10580 |
rs146360273 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434681 | GGAATGATTTTAACA[A/G]CAGAAATAGAGCGTG | 10580 |
rs146384823 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496464 | GTTCCCATTGCCCAG[A/C/G]TGTCCTCCTCCTGCA | 10580 |
rs146395662 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501051 | TTTACTAACCACAAC[A/G]TCCAGTTCTGCACAG | 10580 |
rs146421687 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512235 | CCAGCCTGGCCAACA[A/G]AGCAAAACCCCATCT | 10580 |
rs146431115 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499230 | GGCGTCCACCACCAC[A/G]CCCAGCCAATTTTTG | 10580 |
rs146433395 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465554 | AAAAAAAAGATACTA[A/G]GAAATATACCCTCAC | 10580 |
rs146433748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516762 | TGTCACTCACCTCAA[A/G]TGACTATTTCCAAGA | 10580 |
rs146436630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385031 | AAATCAAACTCACGC[A/G]TGTCTCTATGGTGGG | 10580 |
rs146472238 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352466 | CCCCTAAAGGAGGGT[A/G]GGCCCGATTTTTCTC | 10580 |
rs146509446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468995 | TACACAGAGGAATCA[A/G]GTCCTTCGTCATTGC | 10580 |
rs146521569 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348337 | AAGGAAGTAGGTTAC[C/T]TCATGTCACCCAGCT | 10580 |
rs146533177 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327722 | CTGCTGCTCCCCTAA[A/C]CTGCCTGAGTCTCAC | 10580 |
rs146544099 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533973 | CCACCAGGCTGTCTA[A/G]AAATCATTGTTTTTG | 10580 |
rs146554702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537917 | TGAACTCAGGAGTTC[A/G]AGACCAGCCTTGGCA | 10580 |
rs146582160 | in-del | -/CT | 0.318656 | 0.240388 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547826 | GGGCTAACATCAGAG[-/CT]TCTCTTTCTCCTCAT | 10580 |
rs146591929 | snp | A/C/G | 3.31919e-05 | 0.0040737 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414818 | AACCAGGTAGAGAGG[A/C/G]ACAACTATTACCTCC | 10580 |
rs146592479 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369357 | CAGGGCTTCAACCAT[C/T]GCCTCTCCTCAGGTG | 10580 |
rs146628811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406820 | CTAGAACCTGGATCC[C/T]TGACTCCTAGTCCAG | 10580 |
rs146664543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469811 | CCCCTGCTCTTATCA[C/G]TACACTAAAGGTTCT | 10580 |
rs146669035 | snp | A/G | 0.000677333 | 0.0183904 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95381706 | TTCGTTGGTCAGAAC[A/G]GAAGACTTGCCAGGC | 10580 |
rs146674468 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558136 | TCTACAAAAAGTACA[A/G]AAATTAGCTGGGTGT | 10580 |
rs146676181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425345 | CAGGTATCATGAAGG[A/G]ACCATCACTGTGACA | 10580 |
rs146676237 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473012 | CTCCAGCCTGGGTGA[A/C]AGAGAAAGATTCCAT | 10580 |
rs146678847 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349380 | GCTAACTTTTGCTTC[C/T]TCCTTGATAGATTTT | 10580 |
rs146682094 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369115 | ACTGACCTTCCTGGG[-/A]GTCCACCTTTCTGGA | 10580 |
rs146747446 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428910 | CCATCCACTACCTCA[C/T]ACTTGGGCTCCCAGT | 10580 |
rs146751237 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353044 | TGTAGTTTAACCATA[C/T]AAGCCAAAAACCATG | 10580 |
rs146753982 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473154 | ATGTACAAAATTATT[C/T]ATTATATAATGATTT | 10580 |
rs146787335 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489745 | TCTGGGACTCAGAAT[A/G]TCACTGTGTCCCCTT | 10580 |
rs146796301 | snp | A/C/G | 0.0614824 | 0.164198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493161 | TAAGCATGGTGGCAC[A/C/G]CACCTGTAATCCCAG | 10580 |
rs146798181 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443346 | CTGTAATCCTAGCTA[C/T]TCGGGAGGCTGAGGC | 10580 |
rs146800397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365707 | CACCTGTCATATTGG[C/T]GACTGAGTCACCAAC | 10580 |
rs146860970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330087 | AGGTAGACTTGGGTG[C/T]GGGCCTTTTGAAATG | 10580 |
rs146869096 | snp | A/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448171 | GATTTACACTGGGCC[A/G]TGAGGATCCTTCTAG | 10580 |
rs146872356 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369870 | CCACCCCACCTGCCC[C/T]ACCCATCACCTGTCT | 10580 |
rs146872998 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326191 | CTGCCTTGTCTGAAA[A/T]CAGGCACTATCTATC | 10580 |
rs146890606 | in-del | -/TT | 0.101658 | 0.201233 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468626 | ATGGAACCTGCACTC[-/TT]TTATTATTAATGTAT | 10580 |
rs146896423 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559618 | ACTAACCCTTTCCTA[A/G]CCATCTGCTCCAACA | 10580 |
rs146899401 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474011 | TATCCATTCCTTAGA[A/G]AGAAGTGAATAACTT | 10580 |
rs146909478 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430119 | TAGAAATTTGTAAGA[C/T]ACAAAAGTATTCTGG | 10580 |
rs146910056 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479290 | CCATGTGGCTAGAAG[C/T]GAAGAAGGTCCAAAG | 10580 |
rs146912309 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354766 | CACTTGTGAAAGCCT[C/G]AATTTTTGCCTCTAA | 10580 |
rs146943235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491721 | ATTATTTTTTTCTTG[C/T]GGTACAGAAATATTT | 10580 |
rs146971392 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454662 | AAACGGATCCTCTTT[A/G]GGTGCTTTTTCATCC | 10580 |
rs146983275 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332943 | CACTCATGCAGGGGT[C/G/T]GGGGAGGCTGTCAGG | 10580 |
rs147004353 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495915 | CTATTTCATGTTTGG[A/G]CAGTGTTTTTTTGTT | 10580 |
rs147014378 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450658 | ACGCACACACCACCA[C/T]GCCTGGCTAATTTTT | 10580 |
rs147014441 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499188 | CAAGTGATTCTCCTG[C/T]CTCGGCCTCCCCTAG | 10580 |
rs147017050 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371542 | TGTTATACTTTCATA[C/T]GGCCAAGATAGCATG | 10580 |
rs147047314 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515167 | GCATCAGAATTTCTG[C/T]GATCTCTCCAGACCT | 10580 |
rs147062459 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560171 | AGATGAACCTCCCTC[C/T]TATTGACGATGAAAC | 10580 |
rs147078270 | snp | C/T | 0.00606701 | 0.0547421 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394667 | GTGGGAGTGTAAGGA[C/T]TGTCCTCTGTAGCAG | 10580 |
rs147078576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350122 | TACTGGGATTACAGG[G/T]GTAAGCCACTATGCC | 10580 |
rs147120934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391663 | CTCATTGACTGAGAC[A/G]TGATAACTCTATTTA | 10580 |
rs147151310 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324778 | GAATGAAACGTCTGA[A/T]ATGTCACCTTGAGTG | 10580 |
rs147152593 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450777 | AAAGTGCTGGGATTA[C/T]AAGCATGAGCCACTG | 10580 |
rs147153108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401202 | CCTGGGCAACATAGC[A/G]AGACCCCATCGCTAC | 10580 |
rs147156608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525439 | AAAAGACACCCAATG[C/G]TTTATAGTGAAAAGT | 10580 |
rs147168141 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530693 | ACACACCTGTGGTCC[A/G]CCCTCAACACATTCC | 10580 |
rs147169071 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447101 | AGCTGAGCTCGCACC[A/G]CTGCACTCCAACCTG | 10580 |
rs147190089 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325564 | TACTTCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 10580 |
rs147214898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406032 | GAGGATCTTGGAAGA[C/T]ATTGCTGATTGAATA | 10580 |
rs147220374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328972 | AAAACGAAGACCTGC[C/T]GTGTGTGAATTGGGA | 10580 |
rs147241630 | snp | A/C | 1.79942e-05 | 0.00299946 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337056 | CAACTCAAATGGGGG[A/C]GGCTGAGAGACAGGG | 10580 |
rs147257201 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471003 | CATTGCACTCCAGCC[C/T]GGGCGACAGAGCAAG | 10580 |
rs147257994 | snp | A/G | 1.70571e-05 | 0.00292032 | missense | SORBS1 | GRCh38.p7 | 10:95354958 | ATAAAATGTCTTGGC[A/G]ATTCTGAATCTTTAA | 10580 |
rs147265021 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464721 | CAAACATGTTTTCTT[G/T]GTTTACTTATCTATG | 10580 |
rs147273443 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553118 | CTCAGGAGGCTGAGG[C/T]AGGAGGATCACTTGA | 10580 |
rs147306419 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355462 | GGGGGCTTTGTTTTT[-/A]AAAGAAGTGCAGCCA | 10580 |
rs147308751 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531919 | TTTCAATTACTTTCA[A/G]GCAAAGTCAACTTGG | 10580 |
rs147321083 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426785 | TAACCCGGAGTGTAG[A/C]AGCTTTCAGTAAGTT | 10580 |
rs147340300 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364718 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGACGT | 10580 |
rs147370666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482373 | CCCAGGATTGTAAAA[C/T]CCAAGTATTAGGGTA | 10580 |
rs147380725 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487124 | AATGAAAACCAGGGT[G/T]GATGCCATTCATTAT | 10580 |
rs147423938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324419 | GAAATGTCCTCAACC[A/G]TTAGCAAGCCCTGCA | 10580 |
rs147426816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446303 | TTCCATATTGTCCCC[A/C]CTACCCCGCCAATTC | 10580 |
rs147428538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367348 | ATGCCAGGCAAGAAC[C/T]TGGATTCTAAACTTA | 10580 |
rs147433615 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319131 | GGAGAACATAAAACA[C/T]TTGTTTTTTAAAAAA | 10580 |
rs147444421 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383806 | GCACTATCCTTACTA[A/G]GAATCATGCTATTTT | 10580 |
rs147444892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430612 | TTGCTGCCAGAGGAC[A/G]GGACAGTTGGTTTGT | 10580 |
rs147474632 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504097 | TAAGGGCAGTGACTT[C/T]CTCTCACTGTAGCAA | 10580 |
rs147484546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510074 | ACTATATCTTAATAA[C/T]TCCTTTTCTGATTAA | 10580 |
rs147487449 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427020 | ACCTTCTTATGGTAC[A/C]TTTTTGCTACTGCCA | 10580 |
rs147581710 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442703 | CCAGTCTCTGGTATT[C/T]CTTTATAGCTGTGCA | 10580 |
rs147582348 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394356 | TTGACCAGAGCCCCA[C/T]ATGTTCAAAACATTG | 10580 |
rs147583182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320346 | CCTTCTCCAAGCCAC[A/G]TTGAACCCCCTTCCT | 10580 |
rs147591752 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397069 | TCCCTCCTGTGCTCT[A/G]AAGGTGCATGGCTGG | 10580 |
rs147614281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454942 | TAGTTCTCATGATAT[C/T]AATTTCTTTATAGAA | 10580 |
rs147624800 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460295 | TCACTGAAGTCTACA[A/C]AAGTGACATTAAGAA | 10580 |
rs147631063 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499226 | TACAGGCGTCCACCA[A/C]CACGCCCAGCCAATT | 10580 |
rs147634304 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320859 | CAACACTAATACTGC[A/C/T]GTATCAGAGGTCACC | 10580 |
rs147665695 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363667 | GTTAATTATAAAAAA[-/A]TATATATATTGAAGG | 10580 |
rs147686350 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412717 | TACCTGCTACTCCAG[A/G]CAAACATAATCTGTG | 10580 |
rs147691201 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458542 | CAGGTTAGCCTTGAA[C/T]TCCTGGCCTCAAGTG | 10580 |
rs147696272 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417699 | CAATCTAGGCTCACT[A/G]CAACCTCCGCCTCCC | 10580 |
rs147698353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338041 | CAATTAGAGGACCAG[A/C]CAAGAGGCACCATCT | 10580 |
rs147698472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341915 | GACTAGCCCTTGAAA[A/G]TGCTCAGAGGCCTTA | 10580 |
rs147717980 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473871 | ATGGTCAATTTTGTA[A/T]ATCACCTACTTATTT | 10580 |
rs147719170 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526465 | AGGCAAGGCTGAGAA[C/T]TATTGCTCTAACCCA | 10580 |
rs147727853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478147 | CTTGAAGAAGCCCTC[A/G]TCATATTATAAGAGA | 10580 |
rs147730054 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398072 | CCCATTTCCTCATCT[A/G]TAAGATGGAAATGAT | 10580 |
rs147735523 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522513 | CTTCATGTCAATATT[A/C]AGAACCATGAGGCAG | 10580 |
rs147738377 | snp | C/T | 0.000214297 | 0.010349 | missense | SORBS1 | GRCh38.p7 | 10:95318359 | TTTCCATGACATCAA[C/T]GATATCTCCATCGCG | 10580 |
rs147775535 | in-del | -/AATAAATA | 0.485118 | 0.0849685 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318023 | GTGAGATTCTGTCTC[-/AATAAATA]AATAAATAAATAAAT | 10580 |
rs147792245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401726 | CTCCTCCATGGGGTC[A/G]TGACTGCCCACATCC | 10580 |
rs147802349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361879 | TTTGCCCAAGGTCAC[A/G]GAGTACTTGCTCTGT | 10580 |
rs147826468 | snp | A/C/G | 3.29804e-05 | 0.00406068 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414718 | GTGAGGCGGCAGAGG[A/C/G]AGTCGCTGGGATTGT | 10580 |
rs147828502 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410401 | ACCCAAGAAGTGGAA[C/T]GAACCCAGCTTACTT | 10580 |
rs147831530 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497913 | GAGCCTGGCACATAG[C/G/T]AGGCACTCAATAAAC | 10580 |
rs147834496 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418686 | GGCATGAGCCACTGC[A/G]CCTGGCCTATTTCAT | 10580 |
rs147839715 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546708 | CATCCAAACTGTACC[A/G]TAGGTGAAGCCTCAA | 10580 |
rs147862587 | in-del | -/CCCCCCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407004 | GACCTTTACCTTCCA[-/CCCCCCC]CAGCCGCTAAATATA | 10580 |
rs147897534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423969 | TCAGAGAGGTGGTGG[A/G]AGCCAAAAAGAGCTG | 10580 |
rs147897611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376755 | GACAGAATATACTTC[A/G]TGTTTTAACAAATAA | 10580 |
rs147907293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380908 | GCTGTCCTGCTGGAG[G/T]ACTGCAATGTTTATG | 10580 |
rs147910670 | snp | A/T | 0.000735363 | 0.0191609 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414853 | GGGCTGCACTGGAGG[A/T]AGTGGCATCCTGTGG | 10580 |
rs147937017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521836 | TAATTTTTGTATGTT[C/T]TGCAGAGACAGGGTT | 10580 |
rs147940559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439477 | AGTTCTGCCACTGGA[C/T]GAGAAAGTAGCTTTA | 10580 |
rs147979925 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461322 | CTCAAACTTTCATTA[C/T]ACATTTGTATTCTCT | 10580 |
rs147984288 | in-del | -/GAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415116 | TTATGAGAGAGAAAG[-/GAA]AACAGAACAGGCAGG | 10580 |
rs147984931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530190 | GAATGCCTTCCAAGA[C/T]GCTGGTTCACCTGCT | 10580 |
rs147990301 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414173 | CCTCAGCTCACCACA[C/T]GACCCCCGACCTGGC | 10580 |
rs147992307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339806 | ACTTAATATTTGGCA[C/T]ATGGACTCCCCAGAT | 10580 |
rs148002632 | in-del | -/AGACTCT | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313376 | TTTGCCTACCTGTAA[-/AGACTCT]AGACTTTGGGACAAT | 10580 |
rs148043859 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409202 | TTTTTAAAGAAACTG[A/C/G]CTGTCCTTCTGGGAA | 10580 |
rs148048877 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481402 | TTCCTCAAAGCCACA[A/G]TCACATCCCTCCCAC | 10580 |
rs148085304 | snp | C/T | 0.000131835 | 0.00811788 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95432521 | TTCCCTGTAGGAAGA[C/T]GAGGCCCGGAGAGTC | 10580 |
rs148085758 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430658 | GGCCAGGGGACTGCA[A/C]ATTAAAGCCTTTCTC | 10580 |
rs148102621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475000 | CTGAAATCAGGTATT[A/G]GAATATAGTAGAATC | 10580 |
rs148106668 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366592 | GTATGCATGCATCAT[C/G]CAGAGTCCTAAGAAC | 10580 |
rs148125292 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560360 | GTAGCAATGTAATAG[A/C]GTAATAAATTCTTGT | 10580 |
rs148139767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426647 | TGCTGGGAAATAATA[C/T]GTCCTGACTCTCCAC | 10580 |
rs148141990 | in-del | -/TACAGCTC | 0.142609 | 0.225759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412189 | ACAAAATATCAGGCA[-/TACAGCTC]TTTAAAGTATAAATG | 10580 |
rs148149604 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383544 | TACATGTTGCATGAG[C/T]AAATGGACATTAAAA | 10580 |
rs148154785 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556161 | GGAAACTTTTTTCTA[C/T]TGTTGTGAAAACAAT | 10580 |
rs148163257 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313085 | CCAGAAAGCTCACCC[C/T]CTCCAGTTCCATAAC | 10580 |
rs148191802 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499427 | AACATTTTATAATTT[C/T]AAAATGTGGCTTCTC | 10580 |
rs148201677 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455162 | TCTATAAAATGGGAA[C/T]AATAACAGCCATCAA | 10580 |
rs148245850 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329236 | CTTAGTCCCTTACCC[-/TT]TTTTTTTTCTATTGT | 10580 |
rs148298307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392128 | GGATGTGCATAGAGC[A/G]CAGGGCCACCTATCG | 10580 |
rs148317101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405088 | TTGCCACCTGCCACA[C/T]TCAAGTGCGGTCAGC | 10580 |
rs148348582 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466179 | GGGCACAGCGGCTCA[C/T]GCCTGTAATCCCAGC | 10580 |
rs148360884 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345509 | GAGATCAGAACCATG[C/G/T]TTGGTTAGCTCCACA | 10580 |
rs148364880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515085 | AAGTGGTATCCACTT[G/T]TCAGCAGACTGAAAA | 10580 |
rs148397322 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473167 | TTCATTATATAATGA[C/T]TTTATGGACAAAAGA | 10580 |
rs148418171 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406493 | TATATGACCCCAGTC[G/T]TGGTACCTTTTGAGG | 10580 |
rs148437596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329906 | TGCTTCTCAGACAGA[G/T]GCTTTAAGGACACAT | 10580 |
rs148439515 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521564 | GCTGGGATGACAGGC[A/G]TGAGCCACCATGCTT | 10580 |
rs148451161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468820 | TGCAGGCTGGGGGCC[A/G]GACAGGGCAGAGTGG | 10580 |
rs148455283 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360434 | TAACTATGTAAACAA[A/G]GTACAATCTAAGAGT | 10580 |
rs148461171 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424324 | GCAGGTTGCCTGTTA[A/C]ATTTCTGCCACTTCC | 10580 |
rs148463074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348290 | AAAATTATAAGGATA[C/T]GAATTTCACAGTGAT | 10580 |
rs148468409 | in-del | -/GACT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483239 | AGTTTTATATTTTTG[-/GACT]TCTATTAAAAGGAAA | 10580 |
rs148471606 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400717 | AGGGCACCACAGTTA[C/T]AGCTGCAAGGCAAAA | 10580 |
rs148477053 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556735 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC | 10580 |
rs148502699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548419 | CTGAATTATTACTAC[G/T]TATGTGTCATGCATA | 10580 |
rs148510606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533156 | GTTCATAAGTCCCTA[C/T]TGAATGTTTCTTTCT | 10580 |
rs148511591 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497399 | CCTGACTCCACCCCA[A/G]TTGTTCAGACCTGGG | 10580 |
rs148513839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417296 | GCTAGATTTTCTTTT[C/G]TTTTGTTTTGTTTTA | 10580 |
rs148520064 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429173 | TCCTCATTTTTTTTT[-/T]CTTTTTGAGATGGAA | 10580 |
rs148534967 | snp | A/T | 0.00148378 | 0.0271972 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355725 | TTAATGGCCCTTGGG[A/T]AGTCCTCCAGGGCCG | 10580 |
rs148550376 | in-del | -/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313217 | AATGAATTAGTGGCA[-/G]GTTTCTTTCCTGAGA | 10580 |
rs148564407 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492762 | GAGCCCCTACAATTT[C/G]GTCTTGTCCAGATCT | 10580 |
rs148565291 | snp | A/G | 0.000228706 | 0.0106912 | missense | SORBS1 | GRCh38.p7 | 10:95367677 | TCTGAAGAAATTTCC[A/G]GAGTAGGGCTGATGG | 10580 |
rs148594321 | in-del | -/TTC | 0.381113 | 0.21286 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365826 | ATATGTCTTCTTAAT[-/TTC]TTCTTATGCTCCTGG | 10580 |
rs148610424 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510330 | TGGGGGAGAAAAAGC[-/T]TTTTTTTTTTTGAGA | 10580 |
rs148628415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368672 | GGAAGGAGAGGCAAA[C/T]TCACCCACTAGCCCC | 10580 |
rs148639385 | in-del | -/AAAA | 0.0444908 | 0.142359 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430471 | AAGAAAACGAAACAG[-/AAAA]AAAAACAAATCCACA | 10580 |
rs148649045 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563366 | CGCCTGTAATCCCAG[C/T]ACTCTAGGAGGCCAA | 10580 |
rs148649690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476888 | TTAAGGTGCTTTTCT[C/T]AAGCACCTTAAGAAA | 10580 |
rs148659423 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511575 | TTGCTTGTTTTTGTC[A/G]TTGTCGTTTCTCAAC | 10580 |
rs148660648 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428295 | CAGACACCTATAGTC[C/T]CAGCTACTTGGGAGG | 10580 |
rs148663473 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395867 | GAAACAGTTTGAACA[C/G]GGGCACACCCAGGTT | 10580 |
rs148679191 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441579 | CTGAATGCTTATATA[C/T]AGCTTACTATGCACA | 10580 |
rs148689107 | in-del | -/TACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447028 | GCCTGTAGTTCCAGC[-/TACA]TGCTCTGGAGGCAGA | 10580 |
rs148689628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318966 | CTGATCTGACAGGAG[A/G]CAGAGCCCAGGTGGT | 10580 |
rs148700737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558057 | ATGCTGGAAGGCCAA[C/T]GCAGGCGGATCGCTT | 10580 |
rs148708429 | in-del | -/TTTATTTATTTATTTG/TTTATTTATTTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494859 | CAATTTTTATTTTTA[lengthTooLong]TTTATTTATTTATTT | 10580 |
rs148724630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380505 | GTGCAAGGTTACCTT[C/T]TATGTTTCTTACGTA | 10580 |
rs148774806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536836 | GGACACTTAAGAGGA[A/G]AAGGGGGCACTAGTA | 10580 |
rs148776905 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452317 | AGGTGGAACACATAT[A/G]TACAGGCCCAAAATC | 10580 |
rs148815707 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506808 | GAAAGCGTTTGAGGG[C/G]GAAGGTAAGAGAAAT | 10580 |
rs148820604 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394176 | AGGGCCCATGAAAAG[A/G]GTTAGTTGCAGGCAT | 10580 |
rs148825832 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460763 | GAGTACAGCCAGAAA[C/G]AAACTGACCCCTTTT | 10580 |
rs148830921 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353586 | GCTCACTGCAACCTG[A/C]ATCTCCCAGGTTCAA | 10580 |
rs148862620 | snp | A/C/G/T | 0.000148314 | 0.00861026 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95321992 | TTGACTCCTGTCGGG[A/C/G/T]GTGACTCTTCGCTGC | 10580 |
rs148879602 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454264 | TCAAAACACACTGAT[G/T]GTGTATGCATTCTGT | 10580 |
rs148891343 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338972 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 10580 |
rs148903580 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379393 | TCAACAAAAAAAAAA[A/C]AAAAAAAAAAAAGAC | 10580 |
rs148964412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523564 | CTGCAGTTTTTAAAA[A/C]ATACATTTAGCACAT | 10580 |
rs148966066 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332067 | GTCCATAAATGCTCC[G/T]AAGGAAAATCCACCT | 10580 |
rs148967969 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407602 | CCAGCCTGGGTGACA[G/T]AGAAAGACCCTGCCT | 10580 |
rs148972714 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555780 | CCACCCTCCCAAGGT[A/G]GGCAGAAGACATACC | 10580 |
rs148974256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470761 | GGCGGGGCACGGTGG[C/T]TCACACCTGTAATCC | 10580 |
rs148978542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362549 | AACCCAGAAAGCTCA[A/G]GAAATCGGTCCCCTT | 10580 |
rs149031261 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357520 | GAGGCCTGAATGTGG[A/G]TCTGAACAAGGCAGG | 10580 |
rs149036635 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419387 | ACACGTGGGCTAGCA[C/T]GCACCAAAGGGACTG | 10580 |
rs149099099 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378072 | GCTGCCCAGAGATAA[A/C]GCTAAAAAGGTGATA | 10580 |
rs149140723 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327973 | TTTTTGGCTTTAATG[C/T]TCTATGATTGCAATG | 10580 |
rs149152472 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370690 | TCTCTCTCTCTTACT[C/T]TCTCTCGTATACCCT | 10580 |
rs149177261 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449363 | TGCCTCAGTCTCCTA[A/C]GTAGCTGGGATTATA | 10580 |
rs149182435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515047 | TCCAAGCAGGGGCTC[A/G]TGGGCACTGGGTAGC | 10580 |
rs149187419 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398454 | CAGGCCTGTGCTGCC[A/G]GGGAGAGCTGGGTCA | 10580 |
rs149193083 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321085 | CTGTTGGTAATTATA[C/T]TCACTTCCACGGTTA | 10580 |
rs149215574 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528919 | GCAAGACTCAGTCTC[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs149229727 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526743 | CATTATTCCAGCGAG[C/G]CTTCACTGTTCTGGA | 10580 |
rs149241444 | in-del | -/ATA | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425448 | GTCTGTGAAATGGAG[-/ATA]ATATCTACCTCTTTT | 10580 |
rs149249947 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329396 | TTTTTTTGTAGAGAC[A/G]TAGTCTCCCTGTGCT | 10580 |
rs149258669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345351 | TTCCTGACTCTAAAG[A/C]CCACAATCTTTGCAG | 10580 |
rs149271052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496175 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10580 |
rs149281178 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451322 | CAACACACAAACTAC[A/C]CCCATTGCTCCCAGT | 10580 |
rs149283075 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373183 | GTTCACCACTGACAG[A/C]AACAGGTCAGTAATG | 10580 |
rs149287660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515944 | TAAGTCCTCAGGGAC[C/T]CAAGAGAGCAGAGTA | 10580 |
rs149291405 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399756 | TCAGGATAACTTATG[A/C]CAAAGTGTTCAGGAA | 10580 |
rs149301874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324025 | GCCTTCTAGATGGGC[A/G]CTTAGAAATCTTTTG | 10580 |
rs149331036 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529679 | AACTCTTGAGGAAAC[A/G]CTGACCTGGTCCAAT | 10580 |
rs149334498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446229 | ACACAGACATTCCAC[A/G]AGAAGAACAAGATGT | 10580 |
rs149342710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474470 | CAGATGAAACATGAA[A/G]CCACATCATGTCTGT | 10580 |
rs149345085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395450 | TAAATCAAAGCTTGT[A/G]TTGTGGACATTCAGC | 10580 |
rs149354855 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355058 | CATCTATTATAAATA[G/T]CAAAATTTTGAAGTC | 10580 |
rs149407133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426125 | TCTATGCTAATTTCA[C/T]TTTGACCTGTTTTAA | 10580 |
rs149429060 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547678 | GTGAGCCGAGATCGC[A/G]CCATTGCATGCCAGC | 10580 |
rs149430144 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463900 | GGTCCACCTAAGTAG[C/T]CCATGGTCACAAATG | 10580 |
rs149433187 | snp | C/T | 6.628e-05 | 0.00575635 | missense | SORBS1 | GRCh38.p7 | 10:95357760 | GATCCCCAGGAGCCC[C/T]GTCTGATTCCCTCTT | 10580 |
rs149440762 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417256 | CAACTGGGAATTAGA[C/T]TATGAGATGAGGAAA | 10580 |
rs149449849 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387126 | TAAAGAAAAAAAAAA[-/A]CAAAAAACACTTGTT | 10580 |
rs149451477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368399 | TGCAGAGAAAAAGCA[A/C]CATAATTCTGTAGTT | 10580 |
rs149481323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544042 | GAGGGGTAAGAGGCA[A/C]GAACCAGGTCAGGAA | 10580 |
rs149483471 | snp | A/G | 0.000511724 | 0.0159875 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95434698 | AGAAATAGAGCGTGC[A/G]CGTAAAGGGTCGGCA | 10580 |
rs149484298 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387982 | TGCTACATCTTTTCT[-/T]TTTTTTTTTTTTTTT | 10580 |
rs149484628 | in-del | -/GAA | 0.0501905 | 0.150254 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561579 | GCGCGGATGGGAGGC[-/GAA]GAAGTGTCCGGCGCC | 10580 |
rs149494392 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410081 | GAGACAAACAGCTGG[C/G]AAGAATGAAGGCCAG | 10580 |
rs149497373 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557134 | AGAGTTAGCCAAAGT[C/T]AGTTACATTGTTCAT | 10580 |
rs149501123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471972 | ACAGCTAACAAACCC[C/T]GATGTGGCAATTTTA | 10580 |
rs149502251 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441259 | GGTTAGTATTAAAAA[C/T]GCAAACACTGTAACC | 10580 |
rs149505053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363593 | GAGTAGTTACCACTA[C/T]TGATTTATAGATCTG | 10580 |
rs149505624 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317645 | GAGACATAGGCTCAG[G/T]CAACATTTTCTTGTG | 10580 |
rs149544742 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486476 | ATTGAGCACAAACAG[C/T]TTTAAATCCTTTTTA | 10580 |
rs149552316 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552860 | ACAAAGGAGACAGAA[C/T]GGAGGCCTATAGGAG | 10580 |
rs149555504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436690 | ATTTACTGGGATGAG[C/T]GTTCATTCCAATTCT | 10580 |
rs149563812 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422789 | CCTGAGTGTTCATCA[C/T]ATCACAAAGCACCCC | 10580 |
rs149565828 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392064 | ACTTGGTGCTGATCT[C/G]TCTTGAATGCCTTTC | 10580 |
rs149637494 | snp | A/C/T | 3.29512e-05 | 0.00405891 | missense | SORBS1 | GRCh38.p7 | 10:95399042 | ATGCCCACTTCATCC[A/C/T]TGGAAACATCGCTTA | 10580 |
rs149654131 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521303 | ATTTACCAGCAGGCA[A/G]AGGTGAACGGCACAC | 10580 |
rs149656778 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438948 | TCAGTTTTTCCATCT[A/G]TGTAATGAGGGTGGC | 10580 |
rs149667252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393808 | CTCAACATCTCATCC[C/T]AGAACAGTATTTAAC | 10580 |
rs149684015 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434427 | TTCCTCCCCACATTC[A/G]CTGGCTCTCAGGAAA | 10580 |
rs149720651 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389184 | TCTGGCTTTACCCCC[C/G]ACACTTAGGAAGAGA | 10580 |
rs149741996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505729 | TGAAATTTTTCAGAG[C/T]AAGGGGTATTTAGAA | 10580 |
rs149755021 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419255 | TGAATATGCACCAGC[A/C]AAAAAAAAAACAAAA | 10580 |
rs149805703 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453910 | CTGACAGATAACTGT[A/G]TATATGAAACACTGT | 10580 |
rs149816259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402132 | CTTGACTGAAAAAAT[C/G]AGGCTGATAGTCCAT | 10580 |
rs149857936 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532208 | CCTCACTGAGCCTCA[C/T]TTCCTCATCTGCACG | 10580 |
rs149859897 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447862 | AGAACACAACAAGCA[A/C/T]GAAGTTTCTGTAAAA | 10580 |
rs149863883 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341130 | TTAAGGGCTGGGCAC[C/T]GTGGCTCATGCCTGT | 10580 |
rs149868391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476428 | AACCTGGTTCTTCCC[A/G]GGCTTTCCTGATAGT | 10580 |
rs149879887 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357204 | TCATTTGTCATAAGG[A/G]CTTTTAAAAAATTTC | 10580 |
rs149908682 | snp | A/G | 0.000585111 | 0.0170942 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337269 | GATGAGGGGGCTGGC[A/G]TGATGAGCTTGCTGT | 10580 |
rs149909874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524928 | ACTGGTGGAATGACG[C/T]AGGGTTCAATTCTTA | 10580 |
rs149931539 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427611 | CAATTTCAAGGGCTC[G/T]CTCTGTCACTCCACC | 10580 |
rs149933436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352396 | GGATAATTCTTAGCA[A/T]TGGAAGACAGTAGGC | 10580 |
rs149951686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549758 | TTCATTTTCATGGTT[A/C]AGATGAATCTGATCT | 10580 |
rs149963720 | snp | C/T | 0.000197778 | 0.00994234 | missense | SORBS1 | GRCh38.p7 | 10:95381741 | ATTCGTAAATGCTCT[C/T]GGGCTCTGCACGATA | 10580 |
rs150006093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545964 | CACATCAGACATACT[A/G]CTCATATGCTCAGCC | 10580 |
rs150014848 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493897 | TGATTGCGATGTCCA[A/G]TATGAAAAGAGTGTA | 10580 |
rs150017078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412602 | CCTGGTACACCTAAA[A/G]CCAACTCGATATGAA | 10580 |
rs150027954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365417 | CACGGGCAGTCAGGA[C/T]TGCCAAAGTGACAAG | 10580 |
rs150033793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320801 | CCCCCGCCTTCCACT[C/T]ACCATTGACCCTTCC | 10580 |
rs150067769 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488911 | ACAGATTCTACTCTT[A/G]CCCCTAGCATCTATT | 10580 |
rs150106716 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547269 | AGCACCCTCACTACC[C/T]GCACCTCCACACGCA | 10580 |
rs150110007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512949 | ACTTCGGGGGTCAGG[A/G]CGAAGTAGTGGACCA | 10580 |
rs150128062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445196 | ACTTTTTGAGTAGCA[A/G]GTTCTGTTGTGTGTT | 10580 |
rs150130170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366704 | TTTTTTTTTTTTTTA[A/G]ATGGAGTCTCACTCT | 10580 |
rs150135098 | snp | A/G | 3.29609e-05 | 0.00405948 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351344 | AGCCTCTTCTTGCTC[A/G]CGTTTAAGTCGTCTC | 10580 |
rs150137609 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378899 | CCAATTCCAAGGCTA[A/G]AAGAGAAAAAAGTAT | 10580 |
rs150148869 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338954 | CTCAGGTGATTCACC[C/T]GCCTCGGCCTCCCAA | 10580 |
rs150170601 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490644 | AATAAATGTAGCAGA[C/T]AGGGGGAGAACTGCC | 10580 |
rs150173212 | snp | A/C/G | 0.0138876 | 0.0822334 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460627 | TAAAGTGGGAGGATC[A/C/G]CTTGAGCCCAGGACG | 10580 |
rs150174960 | snp | A/T | 1.70848e-05 | 0.00292269 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381846 | TCATGACAACTGGCA[A/T]TAGCTTCCGACACGG | 10580 |
rs150181671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439820 | AGGCTAGCTAGGCAC[A/G]GTGGCGGAGAGGGGC | 10580 |
rs150193024 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313863 | TGACCAAGCAGCCCG[A/G]GCGTCACAGGGGCCT | 10580 |
rs150200594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331426 | GCAGAGTTGAGGGAG[G/T]TGGGCAGGTGACTGA | 10580 |
rs150205858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522855 | CTAAAATCTGGACCC[C/T]AGGCAATCCAACAAC | 10580 |
rs150257023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518164 | TCAAAACCTAATGAG[A/G]TAGTTATGGTCCCCT | 10580 |
rs150268855 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395218 | TGAAAGAAATTCAAA[C/G]TGCTTTTAAAAATCC | 10580 |
rs150319718 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470127 | CTTCAACATACAATG[A/C]CATATCTAACTAACT | 10580 |
rs150326115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543391 | GCAACAAGAGAGAAA[C/T]TCTGTCTCAAAAAAC | 10580 |
rs150327171 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455558 | CCCACAGTTAATACT[C/T]ATGGATGTTACTGGC | 10580 |
rs150332105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349692 | GCAAAGGCTAGTTTC[A/G]AACTCCTGGCCGTAA | 10580 |
rs150338095 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405525 | CATTAAATCCAAATC[C/T]CTAGGGGGATGGCCT | 10580 |
rs150359987 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336702 | CTGACCACGTCTGAA[A/G]GCTTCAAGCAGCTCT | 10580 |
rs150362947 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486096 | ATAGCACACACTCCA[A/T]ACAGCAGTGTGGTGA | 10580 |
rs150383707 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419102 | GATTAGAACATCAAC[C/G]CAGAAATAGTAAATA | 10580 |
rs150390223 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480265 | GGACAAACCGGAAAG[G/T]GAAGGGGAAGCAGTG | 10580 |
rs150412194 | in-del | -/TC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362564 | GGAAATCGGTCCCCT[-/TC]TCTCTCTCTCCTTGC | 10580 |
rs150427538 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363454 | AAGCGTTTGCTAGTC[C/T]ACCATCACCATATAG | 10580 |
rs150468710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559404 | GAAACTCTCCAACTA[C/T]AACAAATGAAAGCAG | 10580 |
rs150480114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435671 | AGATCTACAGAAACA[C/G]AGCGGGTAGGGCTGT | 10580 |
rs150481976 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359494 | TCCCACGTTGCCCTC[C/T]AAAAGTGCTGGGATT | 10580 |
rs150498380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372926 | TTTCTTACATAATGA[C/T]CCCTAGGGTGATAAG | 10580 |
rs150514854 | in-del | -/A | 0.313082 | 0.241911 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366031 | CAATGTAGGTAGGAT[-/A]TGTCCCAGAGACCAC | 10580 |
rs150519850 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481717 | ATATGAATGTACTCC[G/T]CATGCCAAAAGGCCC | 10580 |
rs150571045 | snp | A/G | 0.142272 | 0.225598 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561277 | CCCGGCGCTGCCGCC[A/G]CCGAGCGGGCAAGCG | 10580 |
rs150582605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438470 | GAGCAGGGCCACTGC[C/T]CCACCTGGTGCCTGG | 10580 |
rs150612313 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330124 | ACTGTGTGTCACTCT[-/A]CCTCCCCAAACTACT | 10580 |
rs150632989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515856 | CAAATTTGGCCTAAC[A/G]CACCCTATGAGAGAG | 10580 |
rs150635606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431251 | GCAGCAGCTCTCAGA[C/T]GCAGTCCTTGCACTA | 10580 |
rs150641533 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323776 | GAGGACTGCTTGAGC[C/T]GGGGAGTTGGAGACC | 10580 |
rs150645528 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387899 | TTAAGCAAGTTTTCT[A/G]AGTTGCCTCACATTT | 10580 |
rs150655130 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477867 | GAGCTAAAACAAAAC[-/AA]AACACACACACACAC | 10580 |
rs150678312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447595 | GCCTTATTTCTTTGT[A/C]CTTTGCAGATCCACT | 10580 |
rs150685618 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508610 | GAATGTCAGATCAGC[A/G]GGAAAGAGCTTTCCA | 10580 |
rs150695591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463281 | GGTCTTATAATCCAA[C/T]GCACAGAGGGTGCTT | 10580 |
rs150706176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409806 | CTTGAAAACTTTACA[C/T]TTCATGCTGCAAAGG | 10580 |
rs150727380 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524123 | ATAAATAAGCCTGGA[A/C]GACTACAGACCAATA | 10580 |
rs150728850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333542 | CGAGGAGGCCGAGGC[A/G]GGAGGATCACCTGAG | 10580 |
rs150768613 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484095 | TGGGCATGGTGGTGC[-/A]ACCTGTGGTCCCAGC | 10580 |
rs150793237 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396471 | GGTCCAAGGTTACCC[A/G]AGTGCTTGGGGGACT | 10580 |
rs150826169 | snp | G/T | 1.65151e-05 | 0.00287355 | missense | SORBS1 | GRCh38.p7 | 10:95315106 | GAAAAGTACCAAACT[G/T]CTTTGTCCTTCTTGA | 10580 |
rs150845041 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471758 | TACTTCTAGGGGACC[A/G]TGAGGCAGTGACAGG | 10580 |
rs150847343 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392452 | ATTTTTAAAAGATCT[C/G]CAGGGAGGATGTCTT | 10580 |
rs150857177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351650 | AAACTACCTACCCCC[A/G]GCTCAGCCCAAAGCC | 10580 |
rs150877015 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536999 | TTTTTGCGTTCTGAC[C/T]GTGCCACATGGTCTA | 10580 |
rs150878777 | snp | C/G | 0.000459575 | 0.0151518 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337178 | ACGCCTGCCTGGGAC[C/G]CCCACAGTCAGTGAG | 10580 |
rs150887391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487692 | GGCGCCCAACGAGGA[G/T]ATGGAAGAAGCTCAA | 10580 |
rs150909120 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422456 | AGGGATGAAGAAACA[A/G]TTGTTACTTGACATT | 10580 |
rs150911646 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345989 | GTAAAGTTATCTCCC[G/T]AGAGACTGGTCTAGA | 10580 |
rs150912178 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474223 | TCATAAGAAATCCTT[-/A]AAAAAAATAAACATG | 10580 |
rs150933546 | snp | A/C/G | 3.793e-05 | 0.00435475 | missense, synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336524 | CTGCAGTCCTACCTG[A/C/G]CTCCCACCTCTCCGA | 10580 |
rs150947104 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558887 | TGGAGTTGTCAGGAA[C/T]CCTGGAAGACCTTCT | 10580 |
rs150958932 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429413 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGCGCT | 10580 |
rs150960978 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353944 | CTCAACAAAGCAGAA[A/C]AACAGAGAAAAAGGG | 10580 |
rs150983523 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505009 | AGCAGCTGCCGTCGT[A/G]TACAGGATACCAAGT | 10580 |
rs150995324 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381122 | ACTCATAATTGCTTA[C/G]AGATGTAAACTTGTA | 10580 |
rs150998806 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554601 | CCCGGGAGGTAGAGG[C/T]TGCAGTGAGCTGAGA | 10580 |
rs151012293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424913 | GAGAATCAAAGATCA[C/G]GTACATGAAAATACC | 10580 |
rs151044356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484424 | CCAGCCCACTGTCCC[A/G]TGCAAGAATAGAGCC | 10580 |
rs151047285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453423 | GCTCACTGCAACCTC[C/T]GCCTCCCACGTTCAA | 10580 |
rs151049010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376200 | ATCATCTGTTTTTAC[G/T]GACAACAGCAAAAAC | 10580 |
rs151063655 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497508 | CAGACATCCATAGCC[A/G]TGTCTGACTTTTTAT | 10580 |
rs151107341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439658 | GTGCACGGCCTCTTC[A/G]CACACAGCAAAAGCA | 10580 |
rs151120578 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330921 | ACGCACATTTTTCAT[C/G]CAATAAGTTAAGTTG | 10580 |
rs151158664 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517685 | TTGTAGAATGAATCA[C/T]ACCAGAGCAGCTGGG | 10580 |
rs151161354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433227 | TCACAGCAACAAAAA[C/T]GACTCAGAAGGCTAA | 10580 |
rs151172630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325277 | GGTATAAAGAGAGGA[C/T]GTAGACAATCTCTTG | 10580 |
rs151200721 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534576 | TGAATAAACCGTGAA[G/T]GCCAAGGGCAGCAAA | 10580 |
rs151205197 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485741 | TTACTTCTCCAAACC[A/G]GGGCAAAAAAAAAGA | 10580 |
rs151212270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511675 | CCTGGAGAAGCCAGT[A/G]TAGACATGGAAGAGG | 10580 |
rs151222400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465294 | AGCACTGTGGGAGGC[C/T]GAGGAGGGCGGATCA | 10580 |
rs151259322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411959 | GTCCACTAAATAGCC[A/G]CCGCTATTTAGTTAT | 10580 |
rs151275520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459908 | AAGATGCCTTTGCAG[C/T]GTTGGGGTTGCCTCG | 10580 |
rs151316920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479372 | GGATTTCCAAGCTAA[A/G]GGGAAGATCGTACAT | 10580 |
rs151319035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398567 | TTGGATGACATGTGA[G/T]CTCCCATCCAGGGAG | 10580 |
rs180672325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454953 | ATATCAATTTCTTTA[C/T]AGAAAATCTTCATTA | 10580 |
rs180675656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427517 | AGAGATGAGGAGGCT[A/G]ATCGGGAAGCTGTGG | 10580 |
rs180693314 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465639 | TTCTAGATAATGAAA[C/T]ATACTGGTAAATTAG | 10580 |
rs180695423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359183 | CACCTCTTGGTGAGG[C/T]GTCCTATGTGGCAGG | 10580 |
rs180697034 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517219 | AGTAGAGGCCATATT[C/T]TATTTTTGCCCTGAA | 10580 |
rs180701986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444818 | ATGATAAGTAATCAC[C/T]GTCATATGCGGGTAG | 10580 |
rs180702249 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495739 | CTCCTTGTTCCAGAT[C/G]CAAGGCCCAAGCTGC | 10580 |
rs180705370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412579 | GGACCCTGTCCCAAC[A/G]AATCTGTCCTGGTAC | 10580 |
rs180706370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380099 | TGTACGTGCTCACCA[C/T]CATTCTCCAAGAAGG | 10580 |
rs180707985 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95400884 | CCCCAGAAATTGAAG[C/T]AGAGGAGGAGGCGGC | 10580 |
rs180719673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434474 | ACATACACAGAGGAA[G/T]TAAGGAAGCAAGCTG | 10580 |
rs180722342 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475507 | CCTCACAGGATTTCT[A/G]TAAGAACCAAAATGA | 10580 |
rs180723018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487128 | AAAACCAGGGTTGAT[A/G]CCATTCATTATAAAT | 10580 |
rs180728208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528744 | GACAACATGGTGAAA[A/C]CCCATTTCTACTAAA | 10580 |
rs180728966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538407 | ACCTGGAAGAGGGAG[C/T]GGAAAGCAACAGCAG | 10580 |
rs180733225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507479 | GTAATTTAATCTTCA[A/G]CTTCAGAATTTCATT | 10580 |
rs180773347 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547682 | GCCGAGATCGCGCCA[C/T]TGCATGCCAGCATAG | 10580 |
rs180816324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348616 | GGTTATACAAAGCAA[C/G]ATCCTCTCCTTCTTT | 10580 |
rs180817855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317726 | ATGCACAATATAAAT[A/G]TAAGTGGAGACTAGG | 10580 |
rs180856588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340020 | GCAGGGTATTCTGTC[A/G]CACACACATATAATG | 10580 |
rs180871705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327870 | ATGCTCTGTACTAAC[C/T]GATTGTCTTGTGAAC | 10580 |
rs180874208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343461 | CCGGCTAATTTTGTA[A/T]TTTTAGTAGAGACGG | 10580 |
rs180891336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430334 | TGTGGTGACGTGCAC[C/T]TCAGCTACTTGGGAG | 10580 |
rs180904982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375194 | TGCAGCTGTAATAAT[G/T]AAGACTTTAAAATAA | 10580 |
rs180920957 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322121 | ATGAACAGATTTTTC[A/C/G]GCAATGTTTATGATC | 10580 |
rs180923705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449327 | CTGCAACCTCCACCC[C/G]CTGGGTTCAAGTGAT | 10580 |
rs180930112 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384633 | TCTGGCTGAGTGGGA[A/C]GCAGGGGCTGAGATG | 10580 |
rs180932971 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407299 | AAACCTCTCGGCCTC[A/C]GTTTCCTTGTCTGTT | 10580 |
rs180933010 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354557 | AGGGTGGGGTTGAGC[A/G]GGGATGAAAGAGCAA | 10580 |
rs180938187 | snp | C/T | 1.71267e-05 | 0.00292627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422082 | CACTCATCTGAGAAA[C/T]AGAGAGGAAAAAATC | 10580 |
rs180972178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394758 | TGACTCTTTCGAATG[A/G]CTGATTACCTATTTT | 10580 |
rs181173164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548563 | CAGGCTCAAGAGATC[A/C]TCCCACCTCAGCCTT | 10580 |
rs181191921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496282 | ATGAAGTTCTAATAT[A/G]CAAAATGAATCCCTT | 10580 |
rs181204486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553755 | AATCAGAAAACAGCA[C/T]TGTAAGCAGGTAACA | 10580 |
rs181205943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455230 | TACATCCAGTGCCTA[C/T]TACAACGTTGGAAAA | 10580 |
rs181213301 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534080 | GGGTGGGACTTGGGG[C/G/T]CCCCAATCATGCAGC | 10580 |
rs181214317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539100 | TGACAAACCCAAACT[A/G]TAAATATTCAGTAAG | 10580 |
rs181219279 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476056 | ACACTATTCTTTTTT[A/T]AAAAAAAGATAAGGT | 10580 |
rs181235354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558017 | ATATAGGCCGGGCAC[C/G]GTGGCTCAAGCCTAT | 10580 |
rs181247226 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517881 | CACAAGTTATTAAAC[C/T]CAAAGGCATCCTCTT | 10580 |
rs181345358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513702 | AAATTAAATTCACCA[A/G]ACATGGGACACCTGG | 10580 |
rs181349074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492054 | AATAAACAAGTACAC[A/G]CACACAATTAACTAA | 10580 |
rs181359773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393728 | ATTCATGGCATTACT[G/T]CCAACGACAGTGCCT | 10580 |
rs181366196 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362793 | ACTGCTCATTTATTC[A/G/T]GTCAACAAATATTTA | 10580 |
rs181367476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420228 | TGATCTGAACACCAC[A/G]GAGATGCTCAATAAA | 10580 |
rs181374197 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438506 | CGCATGCTGGCCCCA[C/T]AGGCTGTGACCTGTT | 10580 |
rs181381630 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353570 | TAATGGCGCCATCTC[A/G]GCTCACTGCAACCTG | 10580 |
rs181383661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331972 | TGACGTTAAGGCACC[A/G]AAACATCTACAGATG | 10580 |
rs181391722 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373979 | CAGTCTCATTAGAAG[A/C]ACTCTGAGGCCTGTG | 10580 |
rs181423566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323556 | GTGGGGCTTCCATTG[C/T]AGAGGCCAGCCTTCA | 10580 |
rs181426304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450941 | TGTTTATAATGTGCT[C/T]ATAATACATTTCTTT | 10580 |
rs181432317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481103 | CCCGGGGCCCCTGTA[C/T]CTCCCCTGCTGTTCA | 10580 |
rs181437866 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439981 | GCTGAGGCAGGAGAA[C/T]CACTTGAACTCAGGA | 10580 |
rs181450756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407705 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCCC | 10580 |
rs181460918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481955 | CCCACTTAATGCCAA[C/T]CTGAGCAGTGCTGAA | 10580 |
rs181472434 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459584 | TGACCACATGGAAAC[C/T]GGCTGGAAAAGCCCT | 10580 |
rs181474024 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420815 | TCATTTCAGCAGCAA[A/G]TGCATTTTTACATCC | 10580 |
rs181491161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542448 | CCTCTCACTGTTCTT[A/C]CAAGATTGGATTTGG | 10580 |
rs181497790 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521544 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATGAC | 10580 |
rs181499595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502872 | TTACTTTTCATCTCC[G/T]GTGCTGATAAACACT | 10580 |
rs181507312 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344839 | TTGGAGGCAGCATGT[C/T]GTGATGAAAACACTG | 10580 |
rs181522546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384998 | TCGGAGTGAGTATCT[A/G]AACTGCATCTCTGGA | 10580 |
rs181523462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471757 | GTACTTCTAGGGGAC[C/T]GTGAGGCAGTGACAG | 10580 |
rs181540732 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321272 | CTTCAAAAACCTTCA[A/G]TGGCTCCCTAGTACC | 10580 |
rs181553426 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343344 | CAGGCTGGAGTGCAA[C/T]GGTGTGATCTCAGCT | 10580 |
rs181573965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459176 | AAGTTTAAAAGATTT[C/T]TATACACTAGATTGT | 10580 |
rs181574846 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408586 | AAAAAAAAGGGGGGG[C/G]GGGGCAGGGAGGGAG | 10580 |
rs181593544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431296 | AACCTGTCAGAAATG[C/T]GAACCTTCAGACCCT | 10580 |
rs181599935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470531 | GTCACCACCCCCACT[A/G]CCTTGTAGTCCATCC | 10580 |
rs181621070 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514275 | CCATGACTGATGCCA[G/T]CTAACTCTGTCCTGC | 10580 |
rs181626468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374827 | GCTGTTCATCCAGGA[C/G]AGCTCAGCTGCTATC | 10580 |
rs181645592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390528 | ACTGCATCTGGCCAA[C/T]TTTCTTCATCTCTTT | 10580 |
rs181652487 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492778 | GTCTTGTCCAGATCT[C/T]CTATTAGCTCTGGGT | 10580 |
rs181656905 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435700 | GTCTGGGAACAAGAC[C/T]GCCACTGCAAAGTCA | 10580 |
rs181664865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328147 | CTGGAAGTATCCCAA[A/G]CGACTGCCCCAAAAT | 10580 |
rs181666468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350672 | TGCTGAACACTTCAC[A/T]CAATTCATCCACCTA | 10580 |
rs181671336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369186 | TTCGCTTTTCCCTCC[A/G]CCTCTGTGAACTCTC | 10580 |
rs181697226 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354493 | TGTGCCAACAGAGGG[C/G]TGGGCAGTATTGGAG | 10580 |
rs181704047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535564 | CACATTCCCCATGTA[C/T]GTATCTGCATATAGA | 10580 |
rs181717172 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311346 | GACAGATTGCATTTT[C/T]GCCCACCCATACCAA | 10580 |
rs181725246 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338866 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTG | 10580 |
rs181784044 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332293 | ACCACCTTCCTTCCC[A/G]GTTATTATTTCTCCC | 10580 |
rs181800878 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378981 | AGGTTTGGTCGCTCA[A/G]GCCTGTAGTCCCAGC | 10580 |
rs181810393 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513092 | TTGTATAAGGTTATG[C/T]GGTGACTGAGAGGGT | 10580 |
rs181810596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490739 | GAAAATATAAGCATT[C/T]GTGCATACATTACTT | 10580 |
rs181814614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425161 | ATACTAACGTCAACA[A/G]GTTCTGAGTGAAGGG | 10580 |
rs181821197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468748 | TTCAGCCTCATTACA[C/T]AGAGAAGGACTGAAG | 10580 |
rs181902073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543020 | AGACTATGCCCATGC[C/T]GCAGGCAGGGGCCCA | 10580 |
rs181922839 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539565 | GAGTCCTGGCTCTAC[A/G]TTGTACTAATTCCAT | 10580 |
rs181929442 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316607 | ATATATATTCCTGAA[C/T]GAGTTTAACAGCTAT | 10580 |
rs181935013 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547315 | ACCTTCCTATTTCAT[A/G]GCCTGAAATGCACTG | 10580 |
rs181939916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497157 | CAACACATAGCAAGT[A/G]CTCAGTAAAACGTTG | 10580 |
rs181963207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357857 | AAAAAATAAAGATAA[A/G]AATAGGAGTTAGTGC | 10580 |
rs181971471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379503 | TGTTTCTTTCATCTT[C/T]CTGGAATGATTTAGA | 10580 |
rs181982282 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316894 | TCAATGTGGCTTCTA[C/G]AAAATTTTAAATTTC | 10580 |
rs181994714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358475 | CCTGACATGTAGTAT[A/G]AGCATAAACAATTGC | 10580 |
rs181996288 | snp | C/G | 0.000577124 | 0.0169773 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95339241 | ATCCACGTAGGTGAT[C/G]GGGAAGATGCCTTGT | 10580 |
rs182006439 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460573 | AATAATTAGTCGGGC[G/T]TGGTGGTGTGTGCCT | 10580 |
rs182033079 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503280 | CTAAATGTCACCACT[C/T]AGATCAGCTGGGCCC | 10580 |
rs182039817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533652 | GTGGTTTTAGGAAAC[C/T]GTCTGCTAACATTCA | 10580 |
rs182064578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399687 | GTTTTCCTATCCAAA[A/T]ACAGGGATAACACTT | 10580 |
rs182064911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329582 | AACGTCTCTCCCCAT[C/T]CCGTAAGCTGTTAAA | 10580 |
rs182077168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476683 | AAAATGATGATGTGA[G/T]AATCATTTTAATTAG | 10580 |
rs182080397 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351675 | AAAGCCTCTTGCTTC[G/T]GGCAGCAAAAGGCCA | 10580 |
rs182083849 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455837 | TACTCAGGAGGCTGA[C/T]GCAGGGGGACTGATT | 10580 |
rs182085308 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415261 | AGTCTCTGGATTCCA[C/G]GCTCCGGCATACTTA | 10580 |
rs182091066 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435770 | GCATGTCGGCCAGAG[A/G]CAGTGCACCTTCCAG | 10580 |
rs182154211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489087 | CTCTCCCTCCCTATG[A/G]ACACCCCCCAGCCCA | 10580 |
rs182159288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380938 | GGAGCTTTGGAGAAC[C/T]CCTTAACCAGGATCA | 10580 |
rs182161147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540080 | CTCCAGACTCCTCTA[A/G]TTCTCATTCCCATTC | 10580 |
rs182162398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518815 | TACATTTAAATATCT[A/G]AACCTCCCTCCCTCC | 10580 |
rs182162685 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403638 | ACGATCTCAGCTCAC[C/T]GCAACCTTCGCCTCC | 10580 |
rs182165710 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466613 | AGAAGCATGTGCACA[C/T]GAAAGAGAGCTCGTT | 10580 |
rs182166470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558508 | CTCTCATCTTCTAGA[C/T]AGGTAAACGTTCACC | 10580 |
rs182170999 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429489 | TTTTAAGCCCACTCC[C/T]CAGTGTTAACTTATT | 10580 |
rs182172609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448028 | ACTTCCAGTGCACAC[A/G]CATGGCCAAGTCCAA | 10580 |
rs182271902 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312634 | ATGCAAATTTTAACA[C/T]AAGATTTTATTAAAG | 10580 |
rs182277438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333077 | GCTGTCTTTTGTGCA[A/G]GAGATTTGTATTTGT | 10580 |
rs182286373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482409 | AGTCTCATGAGCACC[A/G]GTGAAGACGGGTAGG | 10580 |
rs182304317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444104 | TTATTTTTATTTTTG[C/T]TTTTGTTTTTGAGAC | 10580 |
rs182313810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527073 | GTAAAAACTAGTGTG[A/C]CATGGGTTCTAAATG | 10580 |
rs182317200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440314 | CAAATAAATGGAAAA[C/G]GGTGATTTTTAATCC | 10580 |
rs182321828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522225 | GTGCCTCCTTTTCTC[C/T]CTTTCCTTCTCCTTG | 10580 |
rs182329458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552775 | CAAAGGAAACAGGAT[C/T]CCACCCAGGATAAGG | 10580 |
rs182342628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485915 | AAATCTCTTGGAGAA[A/G]CACCAACACCTAAGA | 10580 |
rs182354914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391835 | TTTATACTGTATAAA[C/T]AACTAGAATTTAGAC | 10580 |
rs182407882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509808 | AAAGTGGCTGCCACC[A/G]GGGCAGCAGGGGGCT | 10580 |
rs182408603 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559359 | CCTACCCACTCCCCA[A/G]TATGCCCAATCTCTT | 10580 |
rs182414884 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477728 | ACAGCAGCATTTATG[G/T]TCAGAGGAAAGTCCA | 10580 |
rs182445307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417809 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGCT | 10580 |
rs182449507 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435863 | TGACTAGGTTGCCAA[C/T]GACGCTGCTGCATGG | 10580 |
rs182452228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436731 | CAGAAATAAATACGG[C/T]AGATCATAAATTCCC | 10580 |
rs182467037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507721 | GTTCGAGCAGCCTGG[C/T]CAACATGGCGAAACC | 10580 |
rs182469959 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457896 | AGAATGTTTCATGAG[G/T]CCAAAGGACTCAGAG | 10580 |
rs182478721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487485 | AAGCTTTGAGGGCAG[A/G]GGGATTGGGGGGTTC | 10580 |
rs182478911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392418 | GGCAGGAGTGGGGGC[C/G]TGAGATGGAATTTAC | 10580 |
rs182483487 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466062 | CTGAGGCAGGAGAAT[C/T]GCTTAAACACGAGAG | 10580 |
rs182504598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530638 | GATCAGAGAGTTGTA[C/T]TGGCAGCACTTGGAA | 10580 |
rs182541851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482796 | CAGAGCTTGAGGAAG[A/G]CCCAGACATGATCTC | 10580 |
rs182557132 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464999 | AGGAATGAAACAAGG[A/G]CTCTACCTTTCAACA | 10580 |
rs182580787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426697 | CTCCGCATTTGGTAC[A/C]TTTTCCAGACTCCAG | 10580 |
rs182596227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507215 | TACAGTTAGAAGATA[C/T]TTGTTCTGGTATTTA | 10580 |
rs182608223 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370495 | TGATCCACTTGCCTC[A/G]GCCTCCCAAATTGCT | 10580 |
rs182641894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334417 | AAGGGGGAGCGAGCC[C/T]CAGGCCACAGCCTGT | 10580 |
rs182665376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422637 | TTTTTCCAGGGGTGC[C/T]GGTGCTGGGCTAAGG | 10580 |
rs182670282 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457752 | GTAGTGACTCCATCC[A/G]GCACCCTGCATTTGT | 10580 |
rs182675988 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549861 | GAAAACAATCCTCTA[A/G]TGTCAAGGCTGTGGT | 10580 |
rs182692210 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325334 | CTAGCCTCCTTCCAC[C/T]CAACTTCATTCATCC | 10580 |
rs182692563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355399 | TCAGTTGAGCTAAAC[A/G]GCCAATTTTTCTTTC | 10580 |
rs182694094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461866 | AGGGTTTCCGAGTGA[G/T]AAGTTTACTAGGACT | 10580 |
rs182695708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375285 | TATTTTATATTCCTT[C/T]GGGTGCAAGGCTAAG | 10580 |
rs182701524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440533 | TGGAAAGCTGACAGC[C/T]CTTAGCTGCATGATG | 10580 |
rs182708714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395527 | GGCAGGTAGTTTTGT[C/T]TAGCACCTACAATTT | 10580 |
rs182709815 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536467 | TTTGGGGGTTTTTTT[A/T]AATCAGTCATAACCT | 10580 |
rs182715035 | snp | C/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515549 | GTAATTTTTTAAAAA[C/G]TTGTCTATCTCAACT | 10580 |
rs182729576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497747 | TCACCATCACCACCA[C/T]CCCACCCCCAGGCTA | 10580 |
rs182783085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504588 | TATACGTGTATCCCC[A/G]GACAAATCTTTTAAC | 10580 |
rs182788159 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483634 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCTG | 10580 |
rs182794133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463050 | TTAAGAACTATCATG[A/C]CTCATACTACAAAGC | 10580 |
rs182859195 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409254 | GAATTTTTTTTTTTT[A/T]AAATATGAGTCACAA | 10580 |
rs182874930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345508 | GGAGATCAGAACCAT[A/G]GTTGGTTAGCTCCAC | 10580 |
rs182888607 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363101 | TCCTCCATAAAGCTT[A/C]ACCTTTCTTCCTCCA | 10580 |
rs182893342 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385534 | CAGAATATTTTATGA[A/G]ATATAAATAAGCTAA | 10580 |
rs182908133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324754 | TACCTTCTATGTGGG[C/T]TTTCAGAAGAATGAA | 10580 |
rs182919722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427734 | CATTCTCCTGGAAGT[C/T]CTTCCCTTGCCAAGA | 10580 |
rs182924415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364404 | TCCAATCCTGCTAAC[C/T]CAATATCATAAATAG | 10580 |
rs182944786 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352472 | AAGGAGGGTGGGCCC[G/T]ATTTTTCTCCAAAGA | 10580 |
rs182945043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330044 | TCATTGTAAAAGACT[A/G]GAGGCTCTTAACCTG | 10580 |
rs182955781 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532011 | TCAGGAAAGCCTCCT[A/G]CCACAAATAAATGCA | 10580 |
rs182966197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498789 | GCCTCCCAAAGTGCT[A/G]AGATTACAGGCATGA | 10580 |
rs182988744 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523904 | GCAGCAAGACCATGG[C/G]TGATTTCCACTTTTT | 10580 |
rs182988972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544373 | GGACCCTCACATCAC[C/T]CCTAACCCATGGACC | 10580 |
rs182989203 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540737 | TCTGTCTCTAAAGAC[A/C]GAAGGCCTTAAGTTT | 10580 |
rs183003196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522900 | CCCCAGAGGTGGACA[A/G]GAGTGAGACAGGACT | 10580 |
rs183016024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452891 | ACAAAAAGCCGGGTA[A/G]GAAGAACTCAATTTG | 10580 |
rs183053104 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494053 | CTGCATCACACTATG[A/T]CAACCACAACTTCTT | 10580 |
rs183166586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364995 | ATTAAAAATAATGCC[C/T]CATCTTGGAATGTTC | 10580 |
rs183179152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445774 | CATGAAACTACACAA[A/G]TTGAGCTTGACCGGA | 10580 |
rs183194002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411332 | CTGAGATTTGGAGAT[A/T]ATCCTATCCTACTGT | 10580 |
rs183195560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402296 | TGTCACTTTACATAA[A/T]GAAAACCCAAAGTGA | 10580 |
rs183226076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520188 | GCATGGTGGTGCATG[A/C]CTGTAATCCCAGCTA | 10580 |
rs183243426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431818 | TTTCCCAAGTGATGG[G/T]TTAAGGTGGGGAGAT | 10580 |
rs183247088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396381 | CTACTTCACAAGGCC[A/G]AATGTGTTCTCCTTT | 10580 |
rs183252141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478474 | GGTCTAGAAGTATAC[A/G]CTAAGAAGCTTGGGA | 10580 |
rs183271070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520586 | AGGTTGCAGTAAGCC[A/G]AGATCTCGCCACTGC | 10580 |
rs183273521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560211 | CAATTTCAGCAGGTC[C/G]GCCCTGTGACAACAG | 10580 |
rs183280101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473568 | GGGAGGTGGAGGTCG[A/C]AGTGAGCCAAAATCA | 10580 |
rs183283595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503999 | AGCAGTCACAGGCCA[A/G]TTTCTGGGACCCCTA | 10580 |
rs183284536 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560311 | AGGACTGAACAAAAC[A/G]AGCCATGCTCAGTGG | 10580 |
rs183287547 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313866 | CCAAGCAGCCCGGGC[A/G]TCACAGGGGCCTCTC | 10580 |
rs183296819 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441229 | ATGAATGGCAGGTTC[A/G]CGATAAATCCCAATG | 10580 |
rs183297934 | snp | C/G/T | 0.000197737 | 0.00994142 | missense | SORBS1 | GRCh38.p7 | 10:95432528 | TAGGAAGACGAGGCC[C/G/T]GGAGAGTCACCGCTC | 10580 |
rs183306193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544123 | CTGAGGCTGGACGGA[A/G]AACGGTAGGCACCAG | 10580 |
rs183309592 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386621 | AGCCTGGCTGATGGA[C/G]TGAGACTCTGTCTTG | 10580 |
rs183312610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492828 | TGCCACGTGACCCAA[C/T]ATCTGCTGGACTTGA | 10580 |
rs183317375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473202 | GACAGCCTAACTACC[A/G]TTCATAGGCAATTGT | 10580 |
rs183319797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410526 | GGCCTTGGGAAACAA[C/T]GGGATTTGTGAAAAT | 10580 |
rs183321652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451691 | TCAAAATAATAAACA[C/T]AAGCCCAGGACACAG | 10580 |
rs183325589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432376 | AACTCACACCCTCCT[A/G]AGCAAAAACACCAGA | 10580 |
rs183330001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536163 | GACAGACGTAAAGCA[A/G]TTCAGGTTTTACACA | 10580 |
rs183338534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515145 | TAAGTATGTTTCTCA[C/G]ACCCCTGCATCAGAA | 10580 |
rs183346596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540805 | ACTAGCCATCAGTTC[C/T]CTACCTTGAGAATTT | 10580 |
rs183424343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387214 | GGGCAGGAGAGTATC[C/T]GTGAACAAGTTTTCA | 10580 |
rs183463210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346349 | ACTCTACAAACAAAC[C/T]GCTGTGTTTCAAAAA | 10580 |
rs183479746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375401 | GATGCTAGAATTCCT[A/T]ACTCCCATTTCAAAC | 10580 |
rs183491739 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340496 | AATGGACCTGTTTTT[C/T]CCACTAGGTCACACC | 10580 |
rs183499768 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380210 | CTGGTAAACTATTGC[A/G]GTATCAATGAGAAAA | 10580 |
rs183500639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335507 | TAAAAATATTCTCAG[C/T]TCTAGAAGCAATTCT | 10580 |
rs183503967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319676 | AGCAAGTGGAGTCAG[G/T]TCTCAAAAACAAGAG | 10580 |
rs183534314 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402979 | ATAAATGACAATATT[A/G]ATAACCTCAGATGGG | 10580 |
rs183545733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451195 | TCCCATGAAGTTCCT[C/T]AGGAGGATGAAGGGG | 10580 |
rs183551809 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95422882 | TGATCCACATAGCAC[A/G]TAGCACCATGAGGCA | 10580 |
rs183556731 | snp | C/T | 0.000101366 | 0.00711847 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341697 | TTGACAGAAGGTCAA[C/T]GGCATTTTAGCAGAT | 10580 |
rs183567642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360154 | CCCTCTTCCCTTTGG[C/T]TGCATTTTCTGATTT | 10580 |
rs183567737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380745 | TATCTCAGTAGAAGT[C/T]AAATCGATTCTTCTT | 10580 |
rs183680546 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331194 | GATACTTGGCAAGCC[A/T]ATGGCAGAGCTAGAG | 10580 |
rs183682087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353522 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCGCACTG | 10580 |
rs183684954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373495 | GCTGAAATTTCAGTT[A/C]ATTTTGGGTGGCTAA | 10580 |
rs183733899 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359751 | CTCTGGTAGAATACC[A/G]CGACATCTCCACCTT | 10580 |
rs183736080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513381 | GCACAATGTCCCAAG[C/T]AGCAGTTGGCCAAAC | 10580 |
rs183739268 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541082 | TGTTTCTCCTCTCAC[C/G]TCTAAGGGATGGCCT | 10580 |
rs183743254 | snp | C/T | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561890 | TGATCAGTTCCTGGC[C/T]GTCGTGCTACATAAA | 10580 |
rs183748477 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491704 | TTAGTCATTGCCCTT[A/C/G]CATTATTTTTTTCTT | 10580 |
rs183765895 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533705 | ACCCACTGCTGCTGG[C/T]TGCCTCCACAGCTGC | 10580 |
rs183819939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505100 | CCCTTTGGTGTTCAA[C/T]AAGAGATCCACTAAT | 10580 |
rs183834557 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464109 | AGGTGGGAGGATCAC[C/T]AGAGGTCAAGACAAG | 10580 |
rs183844319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546284 | CAGGCTGTATCAGTC[C/T]TTTCTTGCATTGCTA | 10580 |
rs183855308 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314890 | GCCCTGTCTAATACA[C/T]AGTAACCTTAGACAG | 10580 |
rs183890591 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488774 | TGCAACCTAGAAGGC[G/T]CTACCTTCAAAATGT | 10580 |
rs183925059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531332 | CTCCTGGACCCAGTA[A/C]GGTTTTCTCACCGTC | 10580 |
rs183986435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550339 | TCAATGCAGAGAACT[A/G]AATCAAACCTTGACC | 10580 |
rs184007725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328495 | ATACTCAACCAATGC[A/T]CAGCCTTCTCTTCAT | 10580 |
rs184013768 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554821 | GAAACAGACAAGGGA[A/C]CCAGCAATATCAACA | 10580 |
rs184014896 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484138 | TGAAGCATAAGAATC[G/T]CTTGAACCTGGGAGG | 10580 |
rs184015626 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369819 | ACAGTGGCTAATCTG[A/G]TTCCTTCACCCTAAT | 10580 |
rs184052600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524665 | GGCAGAGTTGAATAG[C/T]TACAACAGAGAATGT | 10580 |
rs184055862 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508753 | AACTTTAAGATTCAC[A/G]GTCTTCAACTTTCTT | 10580 |
rs184065379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466223 | GAGGTGGGCTAATCA[C/T]GACGTCAGGAGTTCG | 10580 |
rs184066052 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557441 | TGCTTGCACTGAAAC[A/G]AAATCCATGGAAAAG | 10580 |
rs184071675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549230 | TTGTGGCTAGCATGA[C/G]CGAGAAGCTGAATTT | 10580 |
rs184075302 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447683 | ATGTCACTTCTCTTC[A/G]AATGCACCCTCTACA | 10580 |
rs184077940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538492 | TCTGACTGACCAGTT[C/T]AGCATGGGAGGCTCC | 10580 |
rs184086232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353664 | CACCACCATGCCCGG[C/G]TAATTTTTTTGTATT | 10580 |
rs184087706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374480 | TTGCTTTCCTTGACT[A/G]AAGTATGGCATTATT | 10580 |
rs184119598 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320470 | CTGCAACCTCCGTCT[C/T]GGGAGTTCAGGTGAT | 10580 |
rs184122754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360721 | AATAAATCTGCTAAA[C/T]TTAATTTGTCTAAAG | 10580 |
rs184150715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393903 | AATCCCTGCTATTAG[G/T]ATAATTCTCAAGATG | 10580 |
rs184152495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481399 | ATCTTCCTCAAAGCC[A/T]CAATCACATCCCTCC | 10580 |
rs184156884 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532932 | TAAGATTTCCAGTGT[A/G]TCGGTTCTTCTTTGT | 10580 |
rs184158607 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420426 | AGCACTGTTTCTTGA[C/T]CTGCATAGAGCTGAT | 10580 |
rs184160198 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510318 | AAGGTTTTTGTCTGG[C/G]GGAGAAAAAGCTTTT | 10580 |
rs184160243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393664 | AGCTGAAGTGACCTT[A/G]CTGAACTCTCTGCCA | 10580 |
rs184161486 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459471 | AAAGTTACATCTACA[C/T]GTCATTTAAAATACA | 10580 |
rs184166324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351482 | GGGTGAATGGGGCAG[A/G]AGCTTTAAGACTCAG | 10580 |
rs184172733 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438458 | TGGGCCACACATGAG[A/C]AGGGCCACTGCCCCA | 10580 |
rs184174569 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490007 | GCTCAAATAAAGATG[C/T]ATGGGTTGTTCAGCG | 10580 |
rs184175676 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439077 | AATTAAAAGAATCCA[C/T]CATTTTTACACTGCT | 10580 |
rs184185118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326208 | AGGCACTATCTATCA[C/T]TTCTCTTCTTGAATA | 10580 |
rs184186147 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346990 | AAGACTTCCAATCCT[A/G]TTGGGTAGCCCTCTG | 10580 |
rs184203885 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398750 | TCTGAAAAGTTCTAC[A/G]GCAGAGAAATCTCTC | 10580 |
rs184206813 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484837 | AAAATTAGCTGGGCA[G/T]GGTGGCGCACACCTG | 10580 |
rs184211235 | snp | A/G/T | 0.0130992 | 0.0799295 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428182 | TTGGGAGGCCAAGGC[A/G/T]GGTGGATCATGAGGT | 10580 |
rs184211547 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464578 | TCGCTGTCTAGCCCA[A/C]TCTTTGTCCCACACA | 10580 |
rs184214501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432796 | GTTAGGGGAACATGG[A/C]GGCAATGGTGAGTTC | 10580 |
rs184215299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425153 | TTATGCATATACTAA[C/T]GTCAACAGGTTCTGA | 10580 |
rs184219683 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442843 | TTCTACCTAAAAAAG[C/T]CTGTTGAGATTTTGA | 10580 |
rs184229549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365586 | CCTGTGACTTATTGT[C/G]ATTTTTAGAGCTGAA | 10580 |
rs184234271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391195 | TTCTGCTACTTACTG[C/T]GTAATCTTGCATATA | 10580 |
rs184238526 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453401 | GGAGTATAATGGCAC[A/G/T]ATCTTGGCTCACTGC | 10580 |
rs184239525 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505890 | ACCTTGTTATCCCAT[C/T]GGCAGACTGAGAATG | 10580 |
rs184242807 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387956 | GGACAATGGATAACA[C/T]TGAGTCACTCTTGCT | 10580 |
rs184249310 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411930 | CTGCCTAGGTCAGTC[A/T]ATCTCTTCTGAAAGT | 10580 |
rs184250820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342100 | AGCAGGGCATGCCTT[C/T]GTTGCTTTAAATTGC | 10580 |
rs184306302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419515 | GATTTCTTCTTGTCC[A/G]AAGATAGAAATCAGC | 10580 |
rs184319850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357253 | AAAATAATCTGTGCT[A/G]CAAAGCAGGTGCAAG | 10580 |
rs184323786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377949 | TATTTTATTCCCAAA[A/G]GTTGTCTGCAGATCG | 10580 |
rs184466395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480956 | TTAGGCCAAAGGAAA[A/G]AAAAAAAGGAATAGT | 10580 |
rs184497888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520703 | TTAAATAGTAAAATG[C/T]AGCTTTATGAAATTA | 10580 |
rs184518715 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556955 | AGAAAGAATGAGGGA[A/G]GAGGGCAAGGAGAAA | 10580 |
rs184519769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553523 | AGAGGATCTAATCCA[C/T]AGTAAGACATCAAGA | 10580 |
rs184529361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537503 | ACGCCCCTGGGTAGA[A/G]CGGGTACTCAACAAA | 10580 |
rs184550612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542120 | ACCCAGAAAGTTCTT[G/T]TCCATGTTCTTGAAA | 10580 |
rs184582364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500497 | AGAGTCATGTACACA[C/T]TGGATTTTGAAGACT | 10580 |
rs184602698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459025 | AGCTCTGGTATTTGT[C/G]GAGTTTGGTGAATAT | 10580 |
rs184629657 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485789 | AAAAATGTATTCCAC[A/T]CTCTATTTGTAGTCA | 10580 |
rs184656798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382399 | ATGTCAGTTGCTACC[A/G]TAATTGCATTCTTCC | 10580 |
rs184661934 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547228 | CCTGGCTGAGGCAAG[A/G/T]TGCCACATCCATTAT | 10580 |
rs184662702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453879 | CGTGGGGTCCTGGAC[C/T]AATCTCTATAGCATA | 10580 |
rs184663920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526070 | AACCCTGTGCCTGAC[A/G]CATGCTTGCAGGCTT | 10580 |
rs184669376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506668 | TTTTCTTAAATACTG[A/G]GAAAACCAGCTCCTT | 10580 |
rs184673274 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429895 | ATTCCAAGTGACTCA[C/T]GCAGCACCTGGCACA | 10580 |
rs184685203 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412335 | AAATCAATTAACATG[A/C]CTTTTATTCTTCCTT | 10580 |
rs184685390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516559 | AGGAGATTGAGGCTC[A/G]GATAGATGAAGTAAC | 10580 |
rs184692101 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495273 | TTCTCTGTCCCAACC[C/G]CCCAAAAGACTTCAC | 10580 |
rs184692606 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342822 | GTACCCCTTTGCAAC[G/T]TTTCCATATCCATTC | 10580 |
rs184695267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433782 | CCTCTTGTATTGAAC[A/G]CAATGCACGAAACGC | 10580 |
rs184698849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521261 | AGAGGGACTGAATGC[C/T]ATACCACACCTTCAG | 10580 |
rs184702853 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467880 | AAATTCAACCTTTAC[C/T]ATCTTCTTTTTTTTT | 10580 |
rs184710530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458520 | AAAAGGGCTTTGTTA[C/T]GTTGCCCAGGTTAGC | 10580 |
rs184712289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430018 | ATCCCTTAATTCTTC[C/T]GAGTACAGTATTTGC | 10580 |
rs184721325 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563177 | ATTCAGGGCAACACC[A/G]TTTTAGAATAGCCAA | 10580 |
rs184732370 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361807 | TTCTAATGTTGAAGA[C/G]AGACCATTTGTTTCA | 10580 |
rs184737846 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499472 | GATCTGGCAACACAG[C/G]GCCTCAAGGATAACA | 10580 |
rs184738704 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383135 | GGGGCTAGAAGATGC[A/G]TGGAACTCCTGTCCA | 10580 |
rs184741456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437419 | CAGATGGGATGGCCC[C/T]GGCCTGACATACTCC | 10580 |
rs184744109 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479337 | TAAGACTGAAGACAC[A/C]GGGCTTGTTCCAAGC | 10580 |
rs184747376 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406612 | ACACTTGTAAACTTT[C/G]CAACAACTCTAGTAG | 10580 |
rs184809256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406050 | TGCTGATTGAATATC[A/G]GGCGGTGACCGGAAG | 10580 |
rs184834766 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361404 | TAACAAAACATGCTT[C/T]TTCCAGATGGGTAAC | 10580 |
rs184835405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496137 | ACCATGTTGGCCAGG[C/T]TGGTCTCGAACTCTT | 10580 |
rs184840683 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525143 | AAAGTACGGGCTGGG[A/G]GCAGGTCTAAACTTC | 10580 |
rs184841385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321767 | CCAGCAGTCTATGAC[A/G]GCCTTTATTTACCTG | 10580 |
rs184845163 | snp | C/T | 0.000121618 | 0.00779705 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356484 | TCAAAAGCGGTGATG[C/T]GGGAAGAGACGGTGT | 10580 |
rs184845662 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343372 | GCTCACCGCAACCTC[C/T]GCCTCCCGGGTTCAG | 10580 |
rs184848165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335985 | CCCCAGGAGACCTGC[A/T]TTCTCCTCTCCAGAA | 10580 |
rs184849945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455172 | GGGAATAATAACAGC[C/G]ATCAATCTCATAGCA | 10580 |
rs184852611 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448995 | CCACATGTACCACAC[C/T]TGCTATTCCTACTGA | 10580 |
rs184863180 | snp | C/T | 8.32563e-05 | 0.00645145 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376073 | TATAGGGGTTGGTGA[C/T]AGAGAAATGGAAGAA | 10580 |
rs184926160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338711 | CAGTCTGCTTTCCTG[C/T]AGTTTTTTTTTTTTT | 10580 |
rs184940402 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312714 | GTGAGGCTGGCATCA[C/T]ATGCAAATGTGGCTT | 10580 |
rs184946749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546730 | AAGCCTCAAGCACTC[A/G]ATACTTCTTTTTTTG | 10580 |
rs184952498 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355063 | ATTATAAATATCAAA[A/C]TTTTGAAGTCATTCT | 10580 |
rs184952680 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333859 | TTTCCCTTGGCCCCA[A/G]CAGCTTCCTAGAAGT | 10580 |
rs184952811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475712 | TTGCTGGAAGTTATG[A/G]TACTAGGAAGGGGGA | 10580 |
rs184978119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517757 | CAGATAACAAATTGG[C/T]GGTCTGTGACTCAGG | 10580 |
rs185002391 | snp | A/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529031 | GGACCCTACAAAGAC[A/G]GTCAGTTTGGAACCA | 10580 |
rs185038359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399790 | GTACATTGCTAAGTA[C/T]ACATTATAGATTATT | 10580 |
rs185049662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474380 | TTAAACAGCGATATT[A/G]TTTTTAAGCTACTAT | 10580 |
rs185059270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316649 | GCTGCACTCTCTAAA[A/G]TGATAGCCACGTGTG | 10580 |
rs185068506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357978 | CTTATTTAGACAGAC[A/G]TTTCTACAGACAGGC | 10580 |
rs185075544 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315997 | CTAGTTGAACTCCTA[C/T]GGAGAATGGCCAAGA | 10580 |
rs185132101 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379023 | CCAAGAGGGGCAGAT[G/T]GCTTGAGCCAAGGAG | 10580 |
rs185155056 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425236 | CATTATTTTGCCCAC[C/T]TTCTGGTTCTCAGTT | 10580 |
rs185162017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339077 | TGCCATCAGCACTGT[A/T]GACTACAAAAATTCA | 10580 |
rs185181196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449760 | CTTCCAACCCAATAA[A/G]CAAATTCAGCCCCCC | 10580 |
rs185203325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431122 | CACTCCCGCTGCACC[A/G]GAGGGGTCTGCATAC | 10580 |
rs185203634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375199 | CTGTAATAATTAAGA[C/T]TTTAAAATAACTAGA | 10580 |
rs185214016 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394910 | TGACTATGAAAATAA[A/G]ATCTAAAAGCCCAAA | 10580 |
rs185218510 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468957 | CTATGACAATGACAA[C/T]GTGATACGTGTAAAA | 10580 |
rs185263790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559939 | TTAATCCAACCCTCC[A/T]CTCTTCGATCACCAC | 10580 |
rs185269790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462213 | TATTCAGCAACAGAA[A/T]AAGTTTCTTAAAGAA | 10580 |
rs185273752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514082 | CCTAATTTTTTTTTT[G/T]TACACAATCTTGAAC | 10580 |
rs185277216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516360 | TAATAACATGAACCA[C/T]GGTGGTAGATCAACA | 10580 |
rs185287754 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443523 | CTGAATCAGAATGGG[A/C]ATTTTAACAAAATCC | 10580 |
rs185295573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553878 | ATCCTAACTGCCATG[C/T]CTGGCTAATTCTTTG | 10580 |
rs185302302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504189 | GGGTCTGAATGACTC[C/T]CCAAGTCACAGTTTG | 10580 |
rs185315938 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556164 | AACTTTTTTCTATTG[C/T]TGTGAAAACAATAAC | 10580 |
rs185316648 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483009 | TCAGAAAGGAAACGA[C/G/T]GACATGAGAAGAAAC | 10580 |
rs185318686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535106 | GGATGGATGAGTAGA[C/T]GGATACAGATGCCCA | 10580 |
rs185396937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464835 | AATAAAAAACACTGT[C/T]GGGTTTACTGTGTTG | 10580 |
rs185398897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494564 | GGCTCCCTGAATGCA[C/T]CAGCCTGCAGAAATC | 10580 |
rs185404378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547599 | TTAGCCGGGTGTGGT[A/G]GCGGGCACCTATAAG | 10580 |
rs185432210 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536802 | GATTGCAAGACCATG[C/T]AATTTATCATCCAAG | 10580 |
rs185461128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347329 | CTTTGGGTAGTTTCT[C/T]CCTACTCTTACAGAA | 10580 |
rs185467324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424528 | TAACAACTATTTACA[C/T]AGCACTTATATTAGG | 10580 |
rs185480202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388137 | AGCTCCTGCCACCAC[A/G]CCCAGCTTGTTTTTG | 10580 |
rs185487803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380148 | GTTACTTTTCAGGGT[C/T]TGTAAAAACAACGTA | 10580 |
rs185491767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400978 | GGGGTGGGTGCCAGA[C/T]TGCACAGAGGGTTGA | 10580 |
rs185523792 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465791 | CATGATTCTGTGATG[C/T]AGCACATATTCCAGA | 10580 |
rs185531756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444993 | ACTGGAGCAGACACC[A/G]GTTGTAGCACTCTCT | 10580 |
rs185554835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427552 | GGATCTTGAGTTAAG[C/T]CACCACTTGAATGGA | 10580 |
rs185558938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507580 | ACACACATGATCACA[C/T]AGAGGGAGATATGTG | 10580 |
rs185560951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487161 | CATTCCACTGAAACC[C/T]TCATTTGCCATAAAC | 10580 |
rs185583236 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418409 | TTTTTTTTTGAGACT[A/G]AGTCTCGCTCTTGTC | 10580 |
rs185589884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449184 | TTATTTTCTGTAGTT[A/T]CACTGGCTAGAAATA | 10580 |
rs185593405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397618 | TGAAGGAAAGTCTCC[G/T]AGAAATATAAGAGAC | 10580 |
rs185596654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366154 | CCCTCATTGTCATAT[A/T]TCAAAGAACAAGACA | 10580 |
rs185608970 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533120 | TGTCTCACCACCATC[C/T]GAGACACAGACATGG | 10580 |
rs185616948 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441627 | CTTTGAATATATTAA[C/T]GCATTTGACCCTCAC | 10580 |
rs185617962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323898 | GGATCAACTGAGCCC[A/G]GGAGATTCAGGCCAC | 10580 |
rs185624686 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490528 | AAAAGTCAAGGCAGG[A/T]AGCCCCTAACTGGTG | 10580 |
rs185636852 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327083 | AGGTACTCAGCATCT[G/T]CCCTTATTTAAGCCT | 10580 |
rs185717013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468318 | ACCCTTTCTCCAAAC[C/T]GCCCACACTGCCATT | 10580 |
rs185720619 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372435 | AAGATTGACACTGAA[G/T]ATTCCACATTTTTGA | 10580 |
rs185739288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349261 | AGCAGGCAGGACTGT[C/T]AGTGAGGACAAACCA | 10580 |
rs185741117 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330457 | TGTGAACAATGAATT[C/G]AGATAACTCACTACC | 10580 |
rs185746090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512167 | TCACGCTCGTAATCG[C/T]AGCACTTTAGGAGGC | 10580 |
rs185785081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551430 | CAGGAAAAAGATCTA[C/T]CGGCGCTGATATCTA | 10580 |
rs185814482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362753 | CAGTCATCTCTGTCT[A/G]GAAAAGATCTCATCA | 10580 |
rs185838096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352820 | AAAGTATTTGCAATG[C/G]GGAGGGCCTGACTGA | 10580 |
rs185849867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322616 | CTCGCTCTACTACAA[C/T]AGCCACAGAATTCTT | 10580 |
rs185855063 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392751 | TATGGTGGCTGATGA[C/T]ACAGGAGCTCTGGCT | 10580 |
rs185862000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540403 | AATAAAATGAAATCC[C/T]ACCCTACCACTGAGA | 10580 |
rs185948502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384722 | GAAAGGCCTCTTACC[A/G]GGGCCTCGGGCTGCT | 10580 |
rs185955386 | snp | C/T | 4.94686e-05 | 0.00497311 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351238 | TCCTTTTTGCAGTAT[C/T]GTCTATATTGAGGAG | 10580 |
rs185955604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328249 | CAGTCTCCTGGGTTT[A/G]AGCTCCAGGAAACCA | 10580 |
rs185968064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369244 | TCCACATCACCCAAC[A/G]TCCCCATGGGTAGTT | 10580 |
rs185977169 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344380 | AAGAAACTTGTTTAA[C/T]TTTGTTGAACCAAGT | 10580 |
rs186008025 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547728 | TGCCATCTCAAAAAA[C/T]AAATAAATAAAGTAT | 10580 |
rs186013795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508595 | GAAAGTTCCAGACAC[A/G]AATGTCAGATCAGCG | 10580 |
rs186040402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548755 | AGCCACCAGGCCCAG[A/C]CCATAGTTCTAAAGA | 10580 |
rs186060758 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530847 | GTGGAGGACATCGGT[C/G]CCCATACAATACTCC | 10580 |
rs186062467 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440361 | ACACTCACGAAATAC[A/G]GCAGGATTGGGAGAC | 10580 |
rs186115100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522777 | ATCATCCCAATTTAT[C/T]GGAGAAGAAAAGCTG | 10580 |
rs186125440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482606 | TCACTATATTTAGTT[A/C]TTCTTTCGTGTTTAT | 10580 |
rs186158814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317093 | AAATCTTACTGACTT[C/G]TCATTCATGTTGAGG | 10580 |
rs186168780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470657 | CAAGTGCCTTTCTAA[C/T]AGAGCTTCGATGAGA | 10580 |
rs186182321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339969 | AGAAATAGAATTCTA[A/G]ATTTTTAATGGCATT | 10580 |
rs186211292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427028 | ATGGTACCTTTTTGC[G/T]ACTGCCATTCCTGGA | 10580 |
rs186216552 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390734 | ACCTCTGCATCCCAG[A/G]TTCAAGTGATTCTCT | 10580 |
rs186225605 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476137 | GATCAGCCCCACCCC[A/C]ACTCTCCAGGGCAAA | 10580 |
rs186226800 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544143 | GTAGGCACCAGGGAC[C/T]AACAGAGGCCAGTAA | 10580 |
rs186229591 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443028 | GTCTTGTACATACCT[C/T]GACTAATAAGGTCTT | 10580 |
rs186233910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422088 | TCTGAGAAATAGAGA[A/G]GAAAAAATCTCTCAC | 10580 |
rs186235492 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455497 | CAAGAGCACAATCTT[C/G]TCATAACTTTCCATA | 10580 |
rs186236706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358484 | TAGTATAAGCATAAA[C/T]AATTGCTCCTTTATA | 10580 |
rs186237591 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435714 | CCGCCACTGCAAAGT[C/T]AGCATCGTGCTGGTG | 10580 |
rs186238842 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379619 | CCAGAGTTAAGCAGA[C/T]GTAAGTACCTCAAAT | 10580 |
rs186247080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400655 | ATGGCAGAGCTCAGT[A/G]GTGGACAGAAGCAAG | 10580 |
rs186252810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503481 | TTTCCCAGGTCTCTG[C/T]CTATAGCAGAGATTC | 10580 |
rs186278484 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543478 | CTCCCTTCAGACCAG[C/T]AGTCTCCAAACTTTT | 10580 |
rs186289783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476694 | GTGAGAATCATTTTA[A/T]TTAGCACTTTCATTG | 10580 |
rs186292244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456162 | ACACAGACCACAAAA[C/T]GGCCTTGAATACCAG | 10580 |
rs186293917 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357377 | AGAGAGAAAGAGAGA[A/G]AGAGAGAGAGAGAGA | 10580 |
rs186301613 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492146 | GAAGCACCCCACTTT[C/T]CACTAAAATGCTTGC | 10580 |
rs186302181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539672 | ACCTCATGGGGAAGC[A/G]ATGGCAGTTACATAA | 10580 |
rs186311081 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497168 | AAGTACTCAGTAAAA[C/T]GTTGCTGAGTGGGTG | 10580 |
rs186316915 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431447 | GTGGAGAGGTGCTGT[C/T]TCACCCTAAACTAAC | 10580 |
rs186324150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558797 | TGCCATTGTGCAATA[C/G]TTTGAATTTATTATC | 10580 |
rs186331233 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522986 | TAAGGCAGGTGGGAA[C/T]GAATGCTGGGGATGG | 10580 |
rs186346729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385052 | CTATGGTGGGAGGTG[A/G]CTCTCCAAAGGCATG | 10580 |
rs186356863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412610 | ACCTAAAACCAACTC[A/G]ATATGAAAACCTAGG | 10580 |
rs186383357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340031 | TGTCGCACACACATA[C/T]AATGATTTAATTACT | 10580 |
rs186384811 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368489 | AATAAGGGAGTAGTT[A/G]AATAAATCAATGCAA | 10580 |
rs186424354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332097 | TCAGTGCGCTCAGTC[C/T]TCTCTCACTGAGTGC | 10580 |
rs186440782 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345608 | CAGGACAATGGGGTG[A/G]CCACTGACCATTGTA | 10580 |
rs186449514 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363641 | AGTACAAAACTGGAC[A/C]CACACTGTGATGTTA | 10580 |
rs186467638 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407732 | TCCCTTGAGCCCAGG[G/T]GATCAGGACTAGCCT | 10580 |
rs186479829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481956 | CCACTTAATGCCAAC[C/T]TGAGCAGTGCTGAAT | 10580 |
rs186499476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386203 | CATGAAGTAAGAAGC[A/G]AAGTTTTCACTGGGT | 10580 |
rs186502928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521870 | ATATGCATTGCCCAG[A/G]CTGGTCCTGAATTGC | 10580 |
rs186504229 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542592 | GCCCTGGGACTTGAA[A/C]ACAAACAAAGAAAAG | 10580 |
rs186505796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409873 | TCCAAAAAGGAAAAC[C/T]TGGGATTTAGAATCA | 10580 |
rs186510881 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432147 | TTTCAGTCTGCATGA[C/G]AGCAGTCTGCAGAGC | 10580 |
rs186513600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451259 | CCTAAAGAAGCAATC[A/G]CACCAAAACATTTCA | 10580 |
rs186513671 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502946 | TCTCACCTACAAGTA[C/T]TGGCCCTTTCAGATG | 10580 |
rs186514860 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451115 | TGATGCCATCTTCCA[A/C]GGAACTTGTGGGATT | 10580 |
rs186542152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362937 | TTATTTCAAGAAGAA[A/G]AAGAAGAAAAAAAAC | 10580 |
rs186554173 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359290 | ACTGAGAGATTCAGT[A/T]ATTTGTCAAAGTAGG | 10580 |
rs186606424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389658 | GAAGAAGAGAATGAG[A/G]TGGGGCAAAAAATAA | 10580 |
rs186606444 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317867 | ACCTCTACCAAAAAT[A/T]AAAAAATTAGCTGGG | 10580 |
rs186651823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535674 | GGACACTTTTGAAAA[C/T]GAAAGAGGGTGTGAT | 10580 |
rs186693308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489124 | GCCAAACTGCTCCTC[C/T]ACTAAGCCAAGCTTA | 10580 |
rs186702974 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467016 | AGTCATCAAAGACAG[C/G]CTCTAACATGGGTTC | 10580 |
rs186708988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448786 | CATGACAGAGAGAAT[A/G]AGGAATGAATAAATA | 10580 |
rs186727787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550058 | CCTCCTATGTACCAA[C/T]AACTGTGATAGACAC | 10580 |
rs186729357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532564 | GAATCCATTTATACC[C/T]TTCTTTCCAAGAATG | 10580 |
rs186734790 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509994 | GCTATAAAAAGTAAA[C/T]AACACTTTAGGTAAA | 10580 |
rs186807479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555088 | AGGTTTCACCATGTT[A/G]GCCAGGCTGGTCGCG | 10580 |
rs186837404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441060 | GGGGCCTTCAGGGTG[C/T]GTGGGAAATCTGGGT | 10580 |
rs186849170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422678 | GACTTAAGCTGGGAG[A/G]TATCTGCTGCGATAA | 10580 |
rs186871596 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402592 | GGGACTACAGGTGTG[C/T]GCCACCACATCTGGC | 10580 |
rs186877201 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554580 | GAGGCAGGAGAATCG[C/T]TTGAACCCGGGAGGT | 10580 |
rs186887949 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514556 | ACCAGGTATCAAACA[A/G]TGGTCACTCCACCCC | 10580 |
rs186902358 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337461 | AAATCCTCAGGTTAC[A/C]TCTGGGGAGAAACCA | 10580 |
rs186906822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445841 | CTGTTTATTTAGAGA[C/T]AATATGGGCCATTAC | 10580 |
rs186907312 | snp | C/T | 0.0017094 | 0.0291852 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356536 | CCTCCTGGCTGGGGC[C/T]CAGCTCACCCCTGGA | 10580 |
rs186912263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432390 | TGAGCAAAAACACCA[C/G]AGCCTCCTCCCGCCC | 10580 |
rs186912342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377012 | TTCTGGAAATAACTA[C/G]TTGGAAAATGAATGT | 10580 |
rs186925949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315637 | TCCCTATCTTTGGTA[C/T]TAACCTTGTTAGGGC | 10580 |
rs186937638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488208 | AAAGGCTGCTGGATG[G/T]TCCTGCTTGCTAATA | 10580 |
rs186937708 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558018 | TATAGGCCGGGCACC[A/G]TGGCTCAAGCCTATA | 10580 |
rs186940535 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493160 | CTAAGCATGGTGGCA[C/T]GCACCTGTAATCCCA | 10580 |
rs186944554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473474 | GTTTCTATTAAATAC[A/C]AAAATTAGCTGGGCG | 10580 |
rs186952187 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452001 | AACCACAAAATCCCT[A/G]AGGCTATGTATTTAC | 10580 |
rs186953073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518168 | AACCTAATGAGGTAG[C/T]TATGGTCCCCTTTCT | 10580 |
rs186959943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536337 | TCCAAGGAACAATGC[C/T]GGGGTTTAGGAAAGT | 10580 |
rs186964309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397671 | TGTGCCCCCAACCAT[C/T]CTAGATTATTCAACA | 10580 |
rs186965453 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325454 | TTTTACAAGCATATA[C/T]AGATCCATTACATAT | 10580 |
rs186969449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375359 | AATTCAGAGATATCA[C/T]GGGGCAACTGTAGGC | 10580 |
rs186974168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424758 | ATTACTGCAATGTAC[C/T]GGCTTGTATGACCAG | 10580 |
rs186979664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395529 | CAGGTAGTTTTGTTT[A/G]GCACCTACAATTTAG | 10580 |
rs186987445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346845 | ATCTACTTGCTTAAA[C/T]TATGATATGCAAGTA | 10580 |
rs186995209 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507339 | CCTGGGATTACAGAG[A/C]CGCCACCACTCAGAA | 10580 |
rs187003170 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435794 | CTTCCAGTCCATCCC[A/G]CTGTCAGCTCACCTC | 10580 |
rs187021488 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329617 | CTCTATTTAGAGATT[A/T]CCCTTCTGAGTGAGT | 10580 |
rs187035085 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352134 | GAGAATATAAATATT[A/T]AAAAAAAACCCTAAG | 10580 |
rs187039756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536505 | GAAAAATGCCTGTCC[A/G]GGATCCCTGAACTTT | 10580 |
rs187064598 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555758 | ACCAGCAACTGTCGG[C/T]GGGTGCCCACCCTCC | 10580 |
rs187081355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427812 | TCACAAATCCCCCCA[A/G]CTCCATGAGTGCCAC | 10580 |
rs187082940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370889 | AAAGGGTACCCAAAG[A/C]ACTGCTGCTGAGTTT | 10580 |
rs187094436 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391862 | AGACAGAGATGGCAG[C/T]CCTTAGGCTAGGCTT | 10580 |
rs187104929 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496676 | AAAAAAGAAAGCATG[A/C]CTACTTTCAATGATT | 10580 |
rs187127277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539266 | ACATTCTGCATGGGG[C/T]AACTCTGTTACGAGG | 10580 |
rs187146096 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466066 | GGCAGGAGAATCGCT[C/T]AAACACGAGAGGCGG | 10580 |
rs187153228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391396 | ATGTCATTATAAGAC[C/T]ATTATTATTAATAGG | 10580 |
rs187165677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465397 | GCCGGATGTGGTGGC[A/G]AGTGCCTGTAGTCCC | 10580 |
rs187173472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351593 | TTCACTGGAAAAGCC[A/G]GGATAGGGGAAGGAT | 10580 |
rs187178002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527547 | GAGGCCAAATAGCCA[C/T]GTAACAGAAATGTCA | 10580 |
rs187186604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374926 | ACTCAGAAGATGCCT[A/G]AACTTTCAAAGCTCA | 10580 |
rs187197596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420987 | TCTGCTATAGTTTTT[A/G]AGCAGCACAGCTTCC | 10580 |
rs187205745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485933 | CCAACACCTAAGAGA[C/T]GTCGCTGTTGTGTGA | 10580 |
rs187209301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332520 | GCTCACTGCAACCTC[C/T]GCTTCCTGGGTTCAA | 10580 |
rs187239664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429671 | AAACTTCCTAAGGTC[A/G]CAGAGCATTCTGGAG | 10580 |
rs187286984 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504795 | GTCTCAAAGGGGTCC[A/G]TGTTCCAATAAAAAC | 10580 |
rs187291611 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453414 | ACGATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 10580 |
rs187295144 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492791 | CTCCTATTAGCTCTG[A/G]GTCTTAAAAGCCCCT | 10580 |
rs187295827 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483942 | AGAGAGGTATCAGGC[A/T]GGGCGTGGTGGCTCA | 10580 |
rs187320862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524053 | CTAAGAGTAGGAGAC[A/G]TGGGCCAATGTCTCA | 10580 |
rs187320970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474866 | TGATATATGGTTCTC[C/T]TAATTAAGTTTCTCA | 10580 |
rs187358225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415790 | AGAGGAGTTTTCTGA[C/T]GCCGCCAGGCAAATG | 10580 |
rs187366752 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328697 | TTTGTGTAACCCAAA[A/G]TAAAATGATTTTCCC | 10580 |
rs187376663 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444270 | TGGCTAATTTTTAAA[A/T]TTTTTATTTTGTGGA | 10580 |
rs187381810 | snp | A/G/T | 0.00637159 | 0.0561118 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369913 | TGTGCAGTGCCTCTG[A/G/T]TGGCTCCTTCAAGTG | 10580 |
rs187404993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394575 | AAGAAAGTAGCAGCA[C/T]CAGTACGGAGAGGCA | 10580 |
rs187407954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318735 | CCTACTCTACTCTGA[C/T]CTCTGCCTTTAAAGC | 10580 |
rs187426627 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311528 | TTATCAGAACAAATA[C/T]GAACATATTTTAGAA | 10580 |
rs187429695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354548 | GGATTATCAAGGGTG[A/G]GGTTGAGCGGGGATG | 10580 |
rs187470985 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352491 | TTTCTCCAAAGACTA[A/C]AAATAACGAAGTGAC | 10580 |
rs187472106 | snp | C/G | 0.00059998 | 0.0173098 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371942 | CACTAACCAAGGCTA[C/G]AGAGCACACACAGTC | 10580 |
rs187477239 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392567 | ACTATTTCTTCCTTT[A/C]GGTCTCTGAAAATAA | 10580 |
rs187503030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440041 | CCACTGCACTCTAGC[C/T]TGGGTGACAGATCGA | 10580 |
rs187516385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533055 | CCCTCCCTATGGTAC[C/T]GTATATAAACCCTGG | 10580 |
rs187521184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418139 | CTAGAGTGCAGTGGT[A/G]TGACCTTGGCTCACT | 10580 |
rs187528788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437361 | GTGTAGGGAACAGGT[C/T]ACCAGTTTATGGCTT | 10580 |
rs187532417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498315 | TACATGAAATGTCCA[C/G]AATAGATAAATCCAT | 10580 |
rs187533409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499353 | CTGGGATTACAGGCA[C/T]GAGCCACCATGCCCG | 10580 |
rs187534996 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95478712 | ACCCCCACAGAGCCC[C/T]TTCTCTCTCATTTAT | 10580 |
rs187545261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550556 | TCTCAGAATAAGCGA[C/T]GGATTTATTTTTGCA | 10580 |
rs187566776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472108 | TTTTCCAAAGATTCA[A/G]CTTATAACTTAAAAC | 10580 |
rs187603811 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500387 | CTGACCCCTGGCTAC[C/G]TGGACAGCAGGGTAG | 10580 |
rs187605515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524933 | TGGAATGACGCAGGG[C/T]TCAATTCTTAGGCAC | 10580 |
rs187616513 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479386 | AAGGGAAGATCGTAC[A/G]TCATCTTCTTACTTT | 10580 |
rs187625874 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560833 | CCGCTCGCTCCCTCC[G/T]CCTTCCTCTGGCTGC | 10580 |
rs187646853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540849 | TCAGGAAGATTAACC[C/T]CTTCCCTGCTGTGCC | 10580 |
rs187690055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410911 | TCAATGAGATACATC[A/G]TATCATTAATTCCAG | 10580 |
rs187714742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325057 | AATTCTGCATTTCTA[C/T]TTGGTAGTGCTGACA | 10580 |
rs187727242 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441708 | CCGAGACACAGACAG[A/G]TGAAGCTGTGTGCTT | 10580 |
rs187728602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428196 | CGGGTGGATCATGAG[A/G]TCAGGAGTTCAAGAC | 10580 |
rs187736829 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447827 | TTCAGTCTAGAATCC[C/T]ATGACACTCCTGGGA | 10580 |
rs187771581 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484282 | TTTTTAGGATAAGAT[C/T]TTAAACGAACAGTAA | 10580 |
rs187777925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518934 | TCTGTGCAGCCCCAC[C/G]TCCCTCTGGGATGTG | 10580 |
rs187786768 | snp | A/G | 0.000233797 | 0.0108094 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432602 | AAGGTCCAAAATTGA[A/G]GACTGAATCCAAGAC | 10580 |
rs187814151 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473755 | GAATAAAATGGTGCT[C/G]AGGATTTCTTCCAAA | 10580 |
rs187816141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387373 | CATTATTTTAATTTT[C/T]GATGCTTGTCTTGTA | 10580 |
rs187839337 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515839 | GTGTGGATAGGTCTA[C/T]CCAAATTTGGCCTAA | 10580 |
rs187846236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341750 | GACACTTCAGTTTTG[C/T]AGCAAAAGGAGACTT | 10580 |
rs187862447 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360648 | TGTTGCTGGGTGAAG[C/G]TCTCTGAACTGCCCC | 10580 |
rs187864943 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380849 | AGACATTGTGGTGAC[C/T]GTATTTTAATAAAAA | 10580 |
rs187869339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546303 | CTTGCATTGCTATAA[A/G]GAAATACCTGAGACT | 10580 |
rs187888392 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320356 | GCCACGTTGAACCCC[C/T]TTCCTGGGCTCTTCC | 10580 |
rs187902647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324103 | TCCCCTGAGGTCACA[C/T]ATCAAGTCAGTGGTA | 10580 |
rs187914278 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314493 | GTTTTGCCTCTGTTT[A/C]CCCATCCACACCTCA | 10580 |
rs187934477 | snp | A/T | 0.000534045 | 0.0163321 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355701 | GAGTATGGCACGGAG[A/T]TTCCATTATTAATGG | 10580 |
rs187970037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386627 | GCTGATGGAGTGAGA[C/T]TCTGTCTTGAAAAGA | 10580 |
rs188011641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346209 | GGGATCATCACAGCA[C/T]CCACTCCATAAGGAA | 10580 |
rs188016915 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560087 | CGGGGGGCTGGGCGG[C/G]GGGGGGGGTGTTGAG | 10580 |
rs188030656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380990 | CAATGAAGGGTTAAT[A/C]AAAGGATGCATGATT | 10580 |
rs188043977 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505443 | AAGGAATACAGGGAT[A/C]CTGGGTCCAAAACAC | 10580 |
rs188058131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464243 | GGAATCACTCGAACC[C/T]GGGAAGCGGAGGATG | 10580 |
rs188060586 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342291 | CTCTGGGACCTTGGA[C/T]ACAATACTTAATCTG | 10580 |
rs188064703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457782 | TGCAGAACTTTACAG[A/G]CGACAGGACAGCAGT | 10580 |
rs188077875 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417136 | GCATCCCTCTCTTCT[A/C]AACACTGCTCCTCTT | 10580 |
rs188102106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453075 | CGGATTACTTGAGGT[C/G]AGGTGTTTGAGACCA | 10580 |
rs188107765 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513526 | TAAATGCAATCTGAA[C/T]AACACCCCTTTCCAC | 10580 |
rs188110813 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411404 | AAGACTTGTGAGAAT[A/C]CTGACTTTAAAAACC | 10580 |
rs188120386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491864 | ACATTTGCAACCCCC[A/C]AAGAAGTACAACACT | 10580 |
rs188124269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469903 | TGGCCCCAGACTTTC[C/T]ATCTACTTCAGTGGG | 10580 |
rs188134543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553582 | GGGCATGGTGACTCA[C/T]ACCTGTAATCCCAGA | 10580 |
rs188136202 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494271 | CTGTGTGGGTTCACT[G/T]CTCTGGCAGAAGAAA | 10580 |
rs188143843 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534030 | GGGGTCACAGCTATG[C/T]CCCTAATTCCAAGAG | 10580 |
rs188163136 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495508 | CCTTCCTAGCATGAA[C/T]CACTTATATTTTCAC | 10580 |
rs188169113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444471 | TTAACTGAAACTATT[A/T]TCATTCTTTTATAAG | 10580 |
rs188176757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475419 | ACTCCATTTTTCCCC[C/T]TCAAATACGAAACAA | 10580 |
rs188182865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557119 | CTTTCTAGGGCTTGA[A/T]GAGTTAGCCAAAGTC | 10580 |
rs188185194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427365 | AACCAACATGGCCAA[C/T]GCTCAGACCTGGTGT | 10580 |
rs188204887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537889 | TCTGCAAGGCCAAGG[C/T]GGACGGATCACTTGA | 10580 |
rs188214626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393726 | CTATTCATGGCATTA[C/T]TTCCAACGACAGTGC | 10580 |
rs188223737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419928 | CTAAGCCAGTGCATA[C/T]TTACAGCTCTGGCAA | 10580 |
rs188252197 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334532 | CACCAAGAAAGGAAC[A/C]CCAAGTTTCAACAAG | 10580 |
rs188299513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463118 | TCATTTTAAAAACAT[C/T]TTTCCATTGCATTTG | 10580 |
rs188319414 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435869 | GGTTGCCAATGACGC[C/T]GCTGCATGGATTAAG | 10580 |
rs188319997 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495031 | GCTGGGACTACAGGC[A/G]CCTGTCGCCATGCCC | 10580 |
rs188326694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404855 | GTAAGAAAACTGAAG[C/G]CCAGAGACTTAGATA | 10580 |
rs188328062 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454547 | CCTTCCACTTTGCCA[C/T]ATGAACCCAGCCAAG | 10580 |
rs188337071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478081 | GGAGGTTCTTTTTTA[A/C]AAATCTATGATCAGA | 10580 |
rs188343190 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320513 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGCGCAT | 10580 |
rs188361719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360852 | AGAATCTCATTCTGT[C/T]GCCCAGGCTGGAGTG | 10580 |
rs188381736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560224 | TCGGCCCTGTGACAA[C/G]AGGGGCATCCCAACG | 10580 |
rs188490681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350263 | GTTATAAAACAGTAC[A/G]TACTTTGGGTGTTAT | 10580 |
rs188494937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369111 | ATCCACTGACCTTCC[C/T]GGGAGTCCACCTTTC | 10580 |
rs188500700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425154 | TATGCATATACTAAC[A/G]TCAACAGGTTCTGAG | 10580 |
rs188510168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359901 | ATTTCAGGGGACTGC[C/T]GAGGGTGGGGGTCAG | 10580 |
rs188521546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328000 | AATGTGCCTGTCCCA[C/T]GGGTTAAGAAGTAGG | 10580 |
rs188524203 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330107 | CTTTTGAAATGATGC[A/C]AAACTGTGTGTCACT | 10580 |
rs188533735 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485076 | AACTTTTGAGTCCAT[G/T]TTGGGACAATTCTGG | 10580 |
rs188544025 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464610 | GTGACAGGTCCCGTA[A/T]CATTTATTCTTCTCC | 10580 |
rs188551985 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442878 | AATCATGTTGAATCT[A/G]TAGATCAATCTGTGG | 10580 |
rs188552647 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520238 | AAAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 10580 |
rs188558110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390372 | GCTGCAAATTCTGAG[C/T]CATTATTTGAAAATA | 10580 |
rs188560418 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525252 | GAGCCCACAGTGCCC[A/C]GAGTAATACAATCTT | 10580 |
rs188564453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546733 | CCTCAAGCACTCAAT[A/G]CTTCTTTTTTTGTTT | 10580 |
rs188578389 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506254 | GTATGTGCACATGTG[C/T]ACACACATACACACA | 10580 |
rs188593719 | snp | C/T | 0.0087958 | 0.0657308 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437451 | CACCTTTAGAAATGC[C/T]TTCCAGTACCAATCC | 10580 |
rs188596457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516433 | GTATTATCTTAATAC[A/G]TTTGATAATATATCA | 10580 |
rs188620368 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466408 | ATCACGCCACTGTAC[C/T]CCAGCCTGGCGACAG | 10580 |
rs188626438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392892 | TTCCTCTCCACAGGA[A/T]TTCTTCAAGTGGGCC | 10580 |
rs188629063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556610 | GCTGGGGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 10580 |
rs188638691 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549683 | GTGGGAAAACCAAAA[A/G]AAGTTATGAAAAAAC | 10580 |
rs188648976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509310 | TCTACACTCTTACTT[C/T]TATGACCAAAGCAAA | 10580 |
rs188674183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540738 | CTGTCTCTAAAGACC[A/G]AAGGCCTTAAGTTTC | 10580 |
rs188678190 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510959 | CATGCACATTTATCT[C/T]GTTCCATGCAAGCCT | 10580 |
rs188733490 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353523 | TTTTTTTTTTTGAGA[A/C]GGAGTCTCGCACTGT | 10580 |
rs188747934 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373908 | GCATTGATTTAGTTA[A/G]TTTGGCAAGTCTTCA | 10580 |
rs188791268 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341045 | GGGGTTTCACCATGT[C/T]GGCCAGGCTAGTCTC | 10580 |
rs188794134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335587 | CATGTTCCCAGGATC[A/C]TAAGCCCTTGTAATC | 10580 |
rs188805455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380233 | TGAGAAAAACTAAAC[C/T]ATGTTGTTTTTCCTA | 10580 |
rs188833994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423425 | TGATTTTTCTTTCAA[C/G]CATTAAAAAATGTAA | 10580 |
rs188864296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375737 | GCAATGATTATTTGT[C/G]TTTCTCTGGGATATT | 10580 |
rs188866081 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418849 | GGCAGAAGGACCACT[G/T]GAGTCTGAGACCAGC | 10580 |
rs188874060 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433222 | AAAACTCACAGCAAC[A/C]AAAACGACTCAGAAG | 10580 |
rs188882703 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458644 | CTAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 10580 |
rs188891699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488813 | CCTGACCGCTTCTTC[A/G]TATCATTCAATCATC | 10580 |
rs188899793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372807 | CAAAAGATTGTTGTA[A/T]GTTTAATGAGGGAAG | 10580 |
rs188922886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531429 | GCATTTTAGCTGCTA[C/T]ATAACAAACCAGATT | 10580 |
rs189034638 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526422 | TAGTTTTGAAAGCGC[C/T]CCCCTCTCTCAGGCG | 10580 |
rs189036786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506779 | AAACTGCACCCAAGT[G/T]ATTTTTCCAAAGAGA | 10580 |
rs189037946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320878 | TCAGAGGTCACCAGG[A/G]ATTTTTCCAGTTGCC | 10580 |
rs189056508 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343260 | GAAAAAAGAAGGATA[A/C]AAATTATAACCTTTT | 10580 |
rs189065607 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547253 | CATTATGTACCTCTA[G/T]AGCACCCTCACTACC | 10580 |
rs189079970 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481912 | AGTTTTCAAAACTCT[C/G]GTCCCTCCTTTGCTC | 10580 |
rs189082127 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431178 | AAGGGAATGGTCCTC[C/G]CCTCCATTCCATTTC | 10580 |
rs189088915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459551 | GAGCAGGCGGGCTCC[A/G]GAATGTGCCCTAGAC | 10580 |
rs189097770 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439973 | CTCGGGAGGCTGAGG[A/C]AGGAGAATCACTTGA | 10580 |
rs189098907 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500934 | GCACTAACCACGCAT[C/T]TTCTCCCAGCTGGTA | 10580 |
rs189106588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396792 | GGCTTGAGCCACCGC[A/G]CCCGGCCAGAGAACA | 10580 |
rs189113167 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384882 | GAAAACCCTCATCAA[A/C]ATTTGTTTTGATTCC | 10580 |
rs189114675 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521441 | GCATTTTTTTTTTAA[G/T]GGAGTCTTGCTCTGT | 10580 |
rs189118793 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502513 | AGAGCATTTCCCCCA[G/T]CACTCACCTTCCAGA | 10580 |
rs189119199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459072 | AAATCCAGCTTAAGA[A/C]GCATGTAATTGTAGA | 10580 |
rs189126884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541363 | AAGTATCTCCATTCT[C/T]CCAGGCTGGGACCTT | 10580 |
rs189133364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362223 | TAACGGGCAGGTTCC[A/G]GAGGCAGTGGACAGA | 10580 |
rs189138477 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441403 | TTGCCCATATTTGGT[A/G]CTGATGTTATCCGAC | 10580 |
rs189140895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356292 | GTTGGGGAAGCATAG[A/T]CCCCACTGGAGTTCA | 10580 |
rs189149783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383673 | TTCTCTTGTGAAAAT[A/G]CAAAAAGTTATGATA | 10580 |
rs189156038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407073 | CGTGGGTACTGTCAT[C/T]ATTCCCCTTGGCTGC | 10580 |
rs189162048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322108 | CAGTGCTGCAGTAAT[G/T]AACAGATTTTTCGGC | 10580 |
rs189171686 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343377 | CCGCAACCTCCGCCT[C/T]CCGGGTTCAGGCGAT | 10580 |
rs189183035 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468338 | ACACTGCCATTTTGT[C/T]AAGGTACCCACGCAA | 10580 |
rs189201354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527985 | AAATCCAAAACCACA[C/T]TGAGCCACCCTTTGA | 10580 |
rs189211301 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430328 | GCCAAGTGTGGTGAC[A/G]TGCACCTCAGCTACT | 10580 |
rs189217233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486471 | AAAATATTGAGCACA[A/G]ACAGCTTTAAATCCT | 10580 |
rs189226174 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394073 | CTTAGCTAAAACCCT[A/T]ATTTTCAAGAAATGT | 10580 |
rs189235407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420651 | AGGATGCATACGGCT[G/T]TACCTAGGGAGGCAA | 10580 |
rs189328361 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412347 | ATGACTTTTATTCTT[C/G]CTTCTTTCTCTCAAC | 10580 |
rs189356294 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367152 | GGGCTCAAGAGATCC[C/T]CCTGCCTCAGCCTCC | 10580 |
rs189356863 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407429 | TAAAAGATCATGTTG[A/C]CAACATGGCGAAACC | 10580 |
rs189382419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316733 | AAAATACACATTGGG[C/T]TTCAAAGACAGTATG | 10580 |
rs189384365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365662 | GCCAGAGTAGGAGAC[A/G]CGGGTTGTGATGCTA | 10580 |
rs189384587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388047 | TGCAGTGGTGCGATC[C/T]TGGCTCACTGCAACA | 10580 |
rs189389361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362768 | AGAAAAGATCTCATC[A/G]TGTCATTCTACTGCT | 10580 |
rs189389766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481011 | AGGAATGGCCCAGTA[A/G]GGCATGTGGGGTGGG | 10580 |
rs189392566 | snp | A/G | 0.00152628 | 0.0275828 | missense | SORBS1 | GRCh38.p7 | 10:95339161 | GTGGCACTGCGACTT[A/G]GGGAGGAGGAGAAAG | 10580 |
rs189395319 | snp | A/T | 0.142609 | 0.225759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412180 | CCAAGAAACACAAAA[A/T]ATCAGGCATACAGCT | 10580 |
rs189402734 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438477 | GCCACTGCCCCACCT[A/G]GTGCCTGGGCTTCCG | 10580 |
rs189405692 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316357 | ACTTGGGAGGCTGAC[A/G]CAGGAGAAGCACTTG | 10580 |
rs189410053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357577 | CACGGCCGACGCTCA[C/G]TGAATGGAGGTGGAT | 10580 |
rs189413039 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562691 | CAGACTGATCGGAAA[C/T]TCATCAGCAAAGATT | 10580 |
rs189417733 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347275 | GCTGCTCTCAACTTT[C/G]CCTCAGTTCAAATCT | 10580 |
rs189429583 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520749 | TAAAAATAAAGGAAG[C/T]GTTATGCATTCATAC | 10580 |
rs189459209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475817 | GAACATTAATATTAT[A/C]TAATAACTAAATTTA | 10580 |
rs189462118 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465484 | AGTGAACTGAGATCA[C/T]GCAACTGCACTCCAG | 10580 |
rs189464985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435581 | GTGAGGCCTCCCCTC[A/G]TCCTCTCTTTCAAGG | 10580 |
rs189491045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507341 | TGGGATTACAGAGCC[A/G]CCACCACTCAGAAAG | 10580 |
rs189519718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547647 | CTGAGGTTGAACCCG[G/T]GAAGCAGAGGTTGCA | 10580 |
rs189570455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542777 | GGTAGCAGGAGACCA[A/G]GGAGAATGTCATTCT | 10580 |
rs189572429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521954 | GTAAGCCACCACACC[C/T]GGACTTCCTTCTCTA | 10580 |
rs189578906 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503244 | GAGGTGGTGGATGCT[A/G]GAAGCTAATGCCTAG | 10580 |
rs189619797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433994 | CTTCTGAAAGCGCCA[C/T]TGGATAAAGTACTGT | 10580 |
rs189627746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375283 | TCTATTTTATATTCC[C/T]TTGGGTGCAAGGCTA | 10580 |
rs189633843 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395382 | TAGGCAAGAAATATT[A/G]AGTATGATAATAAAT | 10580 |
rs189634788 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348567 | AATTCACTGATTCCA[C/T]TGAACTCTTGAGACG | 10580 |
rs189644105 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312740 | GGCTTTACAAATTGG[G/T]TTTATTTTCTAGCTG | 10580 |
rs189654333 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388199 | TTGTCAAGCTGGTCT[C/T]GAACTCCTGACCGCA | 10580 |
rs189659649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378594 | GCAGGGCTAAATGAC[C/T]ATGCTGAAAAGCCAG | 10580 |
rs189660487 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355284 | ACACACTCACACACA[A/C/T]ATAGGGCCATTGAGA | 10580 |
rs189663821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536358 | TTAGGAAAGTGAATA[C/T]CAGTGAGTTCCACCA | 10580 |
rs189667850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515534 | ATTCTGAAATGGGGG[A/G]TAATTTTTTAAAAAG | 10580 |
rs189672053 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493304 | CAAAAAAAAAAAAGA[A/C]AAAAGAAATAAAGAA | 10580 |
rs189681841 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338858 | GGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT | 10580 |
rs189690123 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422385 | CATAGGAACCCACTC[A/G]AAACCATGATGTGCT | 10580 |
rs189691661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555370 | AAAGCATGGAGGGGT[A/G]GTTCTCAGCACCAGC | 10580 |
rs189698622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440509 | AACTTCTCTGCTCCA[A/G]TTCTGGGTTGGAAAG | 10580 |
rs189703920 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557894 | AGCCTCCTACTTTCT[C/T]GTCTGTTTCTCCAAT | 10580 |
rs189712177 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517779 | TGACTCAGGGCTACC[C/G]GGAAAAGCACACAAC | 10580 |
rs189723298 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496159 | CGAACTCTTGACCTC[A/G]TGATCCGCCTGCCTC | 10580 |
rs189730188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413261 | TCTTCTCCAGACCCA[C/T]TCAGTCAGAAATTCT | 10580 |
rs189743991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455217 | AAATAAGATTCAGTA[C/T]ATCCAGTGCCTATTA | 10580 |
rs189832422 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473519 | TGTAATCCCAGCTAC[A/T]CGGGAGGCTGAGGCA | 10580 |
rs189868123 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358747 | ACACACACACACACA[C/T]ATATTTCTCAGTTAA | 10580 |
rs189872192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379905 | GATGAATTCAACTAC[C/T]GTGAAGGGCAGACTG | 10580 |
rs189875100 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476980 | AAGATAGAGCTACTC[C/T]TTTGACTCAGTCATC | 10580 |
rs189881770 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400878 | AAAAAACCCCAGAAA[C/T]TGAAGCAGAGGAGGA | 10580 |
rs189891736 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317399 | GGCCTCAGTTTTTGA[A/C]TCTGATAAATGAGGA | 10580 |
rs189904055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518802 | AGACTGTTTACCATA[C/T]ATTTAAATATCTAAA | 10580 |
rs189906677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539911 | AAAGGTATCTGAGGT[G/T]AAAGCAAAGGAAAGA | 10580 |
rs189909873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340006 | CTTAATGGACCACTG[C/T]AGGGTATTCTGTCGC | 10580 |
rs189920898 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497169 | AGTACTCAGTAAAAC[A/G]TTGCTGAGTGGGTGG | 10580 |
rs189921239 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464971 | AAAGTCAGAGTGAGC[C/T]TGGGACCTGGACAGG | 10580 |
rs189923528 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379261 | GGTGCGTGCCTGTAG[A/C]CCCAGCTACTTGGGA | 10580 |
rs189936876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425820 | CCAGGGCCATTTGTG[C/T]CTATGTGCAGAAGTA | 10580 |
rs189937736 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558873 | GACTCTAAGAACAGT[A/G]GAGTTGTCAGGAACC | 10580 |
rs189963457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538718 | AATTTTTTTAAAAAA[C/T]AGCACAATTACAGCA | 10580 |
rs189968999 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427706 | CTCCAAATTTCCAAA[C/T]TCCCATTAGAAACAT | 10580 |
rs189977424 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391994 | GGAATGATGGCTCAG[A/T]TTTCTCAGTAACGCT | 10580 |
rs189981462 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417538 | CAATCTCCTGACCTC[A/G]TAATCTGCCCACCTC | 10580 |
rs189993384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445699 | GAATCCCAAGTGGCT[C/T]GGCAGTGGTTGTGTC | 10580 |
rs190007113 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490428 | CAACATATCAGTTTC[A/C]CACTTTAATGTATCT | 10580 |
rs190055370 | snp | A/T | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563251 | ATTGGTTAATAATAG[A/T]ACAACCATATGACAG | 10580 |
rs190059699 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558174 | CGTGCCTGTGGTCCC[A/C]GCTACTCGGGAGGCT | 10580 |
rs190164528 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332158 | TTCTAATAAACTTGC[C/T]TTCTTCAAATCTATA | 10580 |
rs190170358 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485895 | AAGTACAAATGCAAA[C/T]GTGTAAATCTCTTGG | 10580 |
rs190178780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448997 | ACATGTACCACACTT[A/G]CTATTCCTACTGAAT | 10580 |
rs190178936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406338 | TGCCAGTGTGGTGTC[C/T]CCCAGCCTGCCCCGC | 10580 |
rs190179972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399862 | CACATATGACCTAAG[A/G]TTATAAAATTACTTA | 10580 |
rs190183289 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374736 | AAATGAGGTGTGCAC[C/T]AATGCTTTGGGGAGG | 10580 |
rs190184160 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443595 | ACAGAGAAAAACCCC[A/G]GTTCACGAATTCTGT | 10580 |
rs190211901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353071 | CATGGATAAAGACAC[A/C]AAACTTTTAAGAATC | 10580 |
rs190214571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507640 | AGGGCAGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 10580 |
rs190221121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487333 | ACGGGAGGGCCAGAC[C/T]CCATTCTAGAATGCT | 10580 |
rs190225184 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465923 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 10580 |
rs190249865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529256 | ACAGCCACATTCAGG[G/T]GCCTGTTAACAAGGC | 10580 |
rs190249968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548384 | CCCTTCTCAGTCTCA[A/G]TAATAGTAACCAGAA | 10580 |
rs190262580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482401 | GTAGTCCAAGTCTCA[G/T]GAGCACCGGTGAAGA | 10580 |
rs190273316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512392 | CCACTGCTCTCCAGC[C/G]TGGGCAACCAACCGA | 10580 |
rs190276438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542403 | CAGTCTGGGCTCCTG[A/G]GTGGCCTCAAGCTGC | 10580 |
rs190306114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549177 | ACTGCCCATGCCGAC[C/T]GTAGGGCAGTCACTA | 10580 |
rs190356098 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311321 | CACATTTGGTTTGGA[A/G]GAGAAAAAGGACAGA | 10580 |
rs190387695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429920 | GGCACATAGATAATG[A/C]TGAATGAATGTATGC | 10580 |
rs190418784 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468130 | GCGAACTCCCAACCT[C/T]AACTGATCCACCCGC | 10580 |
rs190421903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382470 | AGACCTTAGATTCAA[A/G]TCAGTAATTGATTTT | 10580 |
rs190425450 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354388 | TTATAGGCAACTTCC[A/T]CAAATTGTTTTATAA | 10580 |
rs190505927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422852 | ATGCATTTCAGAGAC[C/T]CTAAACCTCTAGTCT | 10580 |
rs190508501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551904 | AGATAAAGCTGAAGA[C/T]AGCTCTCTGAAAGAC | 10580 |
rs190517052 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533565 | TGCAGAAAGAACAGA[C/T]GAGGACAACCAAAAG | 10580 |
rs190524704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462559 | TTCTTGCTATAAAAG[C/G]TTTGAAATATGGTTC | 10580 |
rs190524803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490534 | CAAGGCAGGAAGCCC[C/T]TAACTGGTGGTCAGT | 10580 |
rs190535363 | snp | A/T | 0.00885091 | 0.0659327 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441120 | GATGAGTTTAAAATG[A/T]CTTACCAGAACTCAT | 10580 |
rs190539011 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391000 | GGCTTAGCAGACTGA[C/G]GCAGGACTGACTCAG | 10580 |
rs190545937 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360024 | GTAGCTTGCAAGGCT[A/G]TGGCACCATATGCCA | 10580 |
rs190548031 | snp | A/G/T | 0.000288028 | 0.0119973 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341239 | TCCCCACATAGCTGC[A/G/T]CCATCCAAGAGAGCC | 10580 |
rs190548974 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554119 | TGCAGTGGCACAATC[G/T]CAGCTCGCTGCAACT | 10580 |
rs190550757 | snp | A/T | 0.000128896 | 0.00802691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414900 | ATGGAAAGGGGTATG[A/T]TACGAGGAAAGAATT | 10580 |
rs190553168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523284 | CCCAGGGCTAGGCTA[C/T]CAGAGAATTATTAGA | 10580 |
rs190559297 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504573 | GACTCCACCACTTTT[C/T]ATACGTGTATCCCCG | 10580 |
rs190562562 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435750 | GTCAAGGCAACAGAA[A/C/G]GGAGGCATGTCGGCC | 10580 |
rs190564568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483398 | GAGTAAATCACATTA[C/T]ACAAAGGACATTATA | 10580 |
rs190576965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319353 | GCATTGAGGGCAAGA[C/T]TTTTATTTACTTGCT | 10580 |
rs190585202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369516 | CCTCACCTTGCCTCT[A/G]CCCTGATCTTCTTCC | 10580 |
rs190591232 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496888 | CTTCCCCAGTCTTTG[C/T]ATTTGCTGTTCTCTC | 10580 |
rs190595077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544161 | CAGAGGCCAGTAAAA[C/T]AAAACAAATGCATAA | 10580 |
rs190598672 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476596 | TCAATGGATGGAACA[A/T]TATTTTATTATTTTC | 10580 |
rs190599074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543876 | CCACTGTTGTCATAA[A/C]CCTACAGGCTGGTAG | 10580 |
rs190603627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330691 | AATTTTTCTATTTTT[A/G]GTAGAGACAGGGTTT | 10580 |
rs190604696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455618 | TTTTTTTTAACTTTA[C/G]CACTTCCTCCAGGAT | 10580 |
rs190705188 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95311810 | TTTATTAAATAATAT[A/G]TACAGCAAATGTAGT | 10580 |
rs190706424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358385 | TGAAATTGGAACCTG[A/G]GATTCTATGGGCTCT | 10580 |
rs190714079 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344674 | CCTCCCAAAGTGCTG[C/G]GATTACAGGTGTGAG | 10580 |
rs190732184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326283 | ACGGTGTACGGTAAT[A/G]GCGTCCAATCATTAA | 10580 |
rs190739808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461537 | GAATTTGCATTTCTG[A/G]CAGATGTCATTTAGG | 10580 |
rs190774123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503730 | AAGTTTCTGAACCTC[C/T]CTGAGCCTATTTCCA | 10580 |
rs190797689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345203 | GTTTTACAGGTATTA[C/T]CCCAGCTTCCCTGCA | 10580 |
rs190800125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363082 | TTCACATTTTATTTG[C/T]ACCTCCTCCATAAAG | 10580 |
rs190804677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385309 | AAATAGTTAGCCTTT[C/T]CCATTTCTAACATCT | 10580 |
rs190808155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370200 | GTTTCCACTTTTCCT[A/G]TCATGGTTTGTGGAC | 10580 |
rs190818135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456210 | GGCCATGAAACCAAG[A/G]AGAGTTCTGCAGAAG | 10580 |
rs190826216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415998 | ACACCTTTGGGAGCC[A/G]ATCCAGCTGCCAGGA | 10580 |
rs190872730 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531685 | TCCACCCCCGAAGAC[A/G]AGCTGTGCAATCCAC | 10580 |
rs190890299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386434 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGACCA | 10580 |
rs190894048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409953 | CGCTTCACCCCAACT[C/G]AAAGCTTCTCTGCTT | 10580 |
rs190904261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432216 | TAACATAAAGTGTGG[C/T]TATTGCTGTGCCTTC | 10580 |
rs190931201 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328982 | CCTGCCGTGTGTGAA[C/T]TGGGAATGTGAACAG | 10580 |
rs190935817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364201 | TCCCCAAATGGTAGA[C/T]TAGCAGGAGGAAAAA | 10580 |
rs191001026 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317916 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGACAGG | 10580 |
rs191006224 | snp | A/G/T | 0.00398731 | 0.0445001 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522791 | TTGGAGAAGAAAAGC[A/G/T]GAGCTCCAAGACTTT | 10580 |
rs191020523 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452038 | ATATATTATACAGAC[A/T]TCTGCAGTACAGACC | 10580 |
rs191029245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482614 | TTTAGTTCTTCTTTC[A/G]TGTTTATTACTGGCA | 10580 |
rs191031544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435860 | CAATGACTAGGTTGC[C/T]AATGACGCTGCTGCA | 10580 |
rs191059705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391551 | ACATCTCTTCCATCC[C/T]GTAGACAGCAGTCTC | 10580 |
rs191076938 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402236 | GTGGTCATGTGACTC[A/T]TCACTGAGTGGATTT | 10580 |
rs191113558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549752 | CTATAATTCATTTTC[A/T]TGGTTAAGATGAATC | 10580 |
rs191133621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492815 | AGCCCCTGCCTGATG[C/T]CACGTGACCCAACAT | 10580 |
rs191138097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557220 | CCTTTGAATGGTTAG[C/T]GCTCTGGTCAACCAC | 10580 |
rs191155475 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451582 | TGGAGCCTTCTCCTT[A/T]GACAATCCAGATAAC | 10580 |
rs191189717 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351634 | GATTACACTGTCCAG[C/G]AAACTACCTACCCCC | 10580 |
rs191220180 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364900 | GTTCCTAATCTGGAT[A/G]TGGCTCTGCCCTGAA | 10580 |
rs191244097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340282 | TTTACTAAGCACCAA[A/C]AAGATACCATGTGTC | 10580 |
rs191244287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464251 | TCGAACCCGGGAAGC[A/G]GAGGATGAAGTGAGC | 10580 |
rs191312120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380206 | GATCCTGGTAAACTA[C/T]TGCGGTATCAATGAG | 10580 |
rs191317316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436314 | GCCACTCCACAGGCA[C/T]TGCCCCTCAGAGTTC | 10580 |
rs191321418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519938 | CAGCACCCAATCTCC[G/T]GCAAAATCAGAAAAG | 10580 |
rs191331699 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478188 | CCTCGTGTTGTTTCC[A/G]CCTCCACCAACTATG | 10580 |
rs191387883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398334 | ACACATGGAAAAGAA[C/T]GGAATTCACCCAAAT | 10580 |
rs191395985 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425066 | AGCTATCACTTTTAC[C/T]GTTCCATCTTCTTTA | 10580 |
rs191404286 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441892 | ATTATACTGACAATG[C/T]CCTAATATATATCCA | 10580 |
rs191413818 | snp | A/C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337537 | GTGTGCAGGCAGGGG[A/C/G]TGGAGGAAGCAGTGA | 10580 |
rs191420096 | snp | C/T | 0.00012507 | 0.00790693 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356600 | AAGATCCCGCACACT[C/T]GAGGAGGAGGAGATG | 10580 |
rs191422269 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377666 | TAGTAAATGGATTCT[A/G]TATTTATTCAATTCA | 10580 |
rs191435037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403494 | AAACTCAGAGAAAGC[A/G]ATAGCATCAGTCTTA | 10580 |
rs191445388 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429146 | ACCATTTCTGAATTA[C/T]CTATACTCACATCCT | 10580 |
rs191455552 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341829 | GGAAGTAAGAACCCC[A/T]CTATTCAGGAAATTA | 10580 |
rs191467343 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360685 | TAAGGGCTGCCTGAA[C/T]ATAAATCCTTCTATG | 10580 |
rs191489729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466418 | TGTACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 10580 |
rs191494525 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322950 | CTATGGCCACCAAGT[C/T]TCCACAACAACAGGG | 10580 |
rs191499253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447972 | AGTCCCTCCAACTCA[A/G]TTTCCGTTCTAACCA | 10580 |
rs191504406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380465 | TAAACCCAAGGAGCA[C/T]GACTTTCTTTGCAGG | 10580 |
rs191529760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457829 | TAAACAGGCCAGTAA[C/T]TGAGTTCAATCTCAA | 10580 |
rs191538642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370993 | TGAAAATTCAGAGAA[A/G]GCAGACAGAGGCAAA | 10580 |
rs191555800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539378 | AAATGACTCTAGACA[C/T]TGCCAAATGTCTCCT | 10580 |
rs191559897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508715 | AGAACTGTTAAAACC[A/G]TGTGGCTTCCAACTG | 10580 |
rs191560852 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498693 | TTTTCTTTTTAATTA[A/T]TTTTTTTTATAGCGA | 10580 |
rs191568468 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428002 | AGGGGTGAGGCCCTC[A/C]TGGCTTCAAACTGAA | 10580 |
rs191571428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329826 | CCTCTGAAGTCACAT[C/G]TTTCTGTCTCAAGTT | 10580 |
rs191573447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352411 | TTGGAAGACAGTAGG[C/T]TTCGTCCAGCAGGCA | 10580 |
rs191579931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451160 | CAGTGACTGCTTTTG[C/T]TTAATGAAAGCCAAA | 10580 |
rs191589988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540670 | TCACATACTATTCAT[C/T]CTTCATGGCTCTGTC | 10580 |
rs191613590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408792 | TATGATTAGTAATAC[A/G]GGGCTGGGCCAGTGA | 10580 |
rs191617422 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492580 | GTAGTGATCTGAGTA[C/T]GCACCTGTGTTATGG | 10580 |
rs191621678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375396 | CTAAAGATGCTAGAA[C/T]TCCTTACTCCCATTT | 10580 |
rs191641937 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531147 | GGCCAGGCTCCCTCT[G/T]CCCACCAAACTGCGA | 10580 |
rs191658449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535199 | GAAGGATGTGAACAA[A/G]TGGAGATGAAGAAGA | 10580 |
rs191699378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525412 | TTTTAATAGATTCCA[A/G]TCACATGGTTTAAAA | 10580 |
rs191701143 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546908 | CACCTGCAAATTTTT[A/T]AAATTTTATTAGAGA | 10580 |
rs191711664 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506526 | TTCCAGGATAGAATT[C/T]CAAAAGATGCTGTAA | 10580 |
rs191753200 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335363 | ACTGAATAACTACAG[C/T]CTCAAAGGGAAACTG | 10580 |
rs191772806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328320 | TCTTATTGAGTTTAC[A/T]GAGAAAAAGATCACA | 10580 |
rs191792635 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446311 | TGTCCCCCCTACCCC[A/G]CCAATTCCATGACCC | 10580 |
rs191810545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354549 | GATTATCAAGGGTGG[G/T]GTTGAGCGGGGATGA | 10580 |
rs191819784 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402735 | CCTCCCAAAGTGTTG[A/G]GATTACAGGTGTGAG | 10580 |
rs191821794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488750 | TCTTGTTTTTACTCA[C/T]ATGCCACATGCAACC | 10580 |
rs191834423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518245 | ATCACATAGTGAATA[A/G]GTAGCAGAGCCAGAA | 10580 |
rs191838150 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440119 | CTCACTAAATCCCAA[G/T]GAACTGGTGTTTTTA | 10580 |
rs191872360 | snp | C/T | 0.000298969 | 0.0122227 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394708 | TGGATTTTGAAACTA[C/T]CCACCAGGAAGTAGA | 10580 |
rs191879877 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520561 | GAGAATCGCTTGAAC[C/T]GGAAGGCAGAGGTTG | 10580 |
rs191885355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489657 | TACATAAGTGTCCTG[C/T]TACCTGATGCCATCT | 10580 |
rs191886139 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499367 | ACGAGCCACCATGCC[C/T]GGCCTTGTAATGATT | 10580 |
rs191890644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467079 | TTCAATGAGTTCTGG[G/T]GTAGAAAAAGTAGGG | 10580 |
rs191896527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448968 | CTCACATCCTCCCAT[A/G]AGCCCTAAACTCCAC | 10580 |
rs191897998 | snp | A/G | 0.00104673 | 0.0228532 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355924 | GGGAAGGTTGTCTGG[A/G]GTGGTGGTGGAGGGG | 10580 |
rs191901069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479132 | TCCAAGGAAGGGGAC[A/G]TCCCTGAAGGAAATG | 10580 |
rs191911908 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532923 | GAAGGCCTCTAAGAT[C/T]TCCAGTGTATCGGTT | 10580 |
rs191918071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540802 | GTCACTAGCCATCAG[C/T]TCCCTACCTTGAGAA | 10580 |
rs191918257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510119 | CTGTTTTTAAAAAGA[C/T]AGAAAATAACTCACC | 10580 |
rs191919575 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470666 | TTCTAATAGAGCTTC[A/G]ATGAGATGAAACAGT | 10580 |
rs191925684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396335 | AGATTATTGTTCGTA[C/T]TAACACAGCCTGAGA | 10580 |
rs191945826 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550302 | GAGAATCCTAGCACC[A/G/T]TGGCTTGCACACAGC | 10580 |
rs191947635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514233 | CTCATACACACACAT[A/T]CAACTAGCCTTATGA | 10580 |
rs192046793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418164 | CTCACTGCAACCTCC[A/G]TCTCCCAGGTTCAAG | 10580 |
rs192046940 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361720 | TTGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA | 10580 |
rs192049522 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382787 | TTAAGTTTTTCATGC[A/G]AGGCTGTAAACTTCT | 10580 |
rs192057756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437371 | CAGGTCACCAGTTTA[C/T]GGCTTGGTTAGGCCA | 10580 |
rs192069437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554714 | ACACACACACACACA[C/T]ACACGCGAAAGTTTT | 10580 |
rs192074361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457960 | CTATGTAATATATCC[A/C]TGTAATACAACTGTA | 10580 |
rs192086575 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515119 | GGTCCAATTCTCTTG[A/G]ATTATCTCCCTAAGT | 10580 |
rs192090609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392669 | ATGCAAAATAAATCC[A/G]GTTCCCCATATGCTG | 10580 |
rs192094727 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332702 | AAGTGATCCGCCTGC[C/T]TCAGGCTCCCAAAGT | 10580 |
rs192096867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365292 | TGCCTTGGATCCAGT[A/G]GAGCTAGGGAATTCA | 10580 |
rs192111947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387374 | ATTATTTTAATTTTC[A/G]ATGCTTGTCTTGTAA | 10580 |
rs192116175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411566 | CATGATATCTATACA[C/T]TTCTATTTTTGAGTT | 10580 |
rs192126503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325812 | TGCCCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 10580 |
rs192134646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346916 | ATATATTTCTTACGG[C/T]CTGTGACATCATCCA | 10580 |
rs192161260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546605 | AAACCACTCATGAGA[A/G]ACTGCCCCTACAATC | 10580 |
rs192162099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375123 | GCATAAAGTCTCATA[C/T]AATCATTGAATAAAA | 10580 |
rs192164435 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345780 | ATTAATATGTCATCA[A/G]CAAAGTATCTCTTCA | 10580 |
rs192173079 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460483 | TTGGGAGGACGAAGC[A/G]GGTGAACCACTTGAG | 10580 |
rs192178295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505699 | ATTACTTAATAAACA[C/T]GGTGTTGGGTTTGAT | 10580 |
rs192181288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421563 | TCTTACAGCCCCATC[C/T]CCAGAAAACAACTGG | 10580 |
rs192239425 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315895 | TGTACACATCTCAAG[A/C]AGCCACTACCAATGG | 10580 |
rs192241368 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485199 | AGCAGGCACCTACCT[A/G]CCACACAGAGCTATC | 10580 |
rs192246500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464823 | TGGAAAGTAGTCAAT[A/C]AAAAACACTGTTGGG | 10580 |
rs192256733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443181 | CGTAGAAGCGGCCGG[A/G]TGTGGTGAGTCACAC | 10580 |
rs192268069 | snp | A/G | 5.05089e-05 | 0.00502513 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432436 | GAACAGCTTTCCCTA[A/G]CTTCCGCGCACCTGG | 10580 |
rs192301428 | snp | C/T | 0.109861 | 0.207029 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95387007 | TGCAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 10580 |
rs192334325 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373180 | TGTGTTCACCACTGA[C/G]AGCAACAGGTCAGTA | 10580 |
rs192375055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488823 | TCTTCGTATCATTCA[A/G]TCATCACTACTCTAA | 10580 |
rs192401945 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335623 | CTCTTTGAGGTAGGT[A/G]CTATCATCTCCATTT | 10580 |
rs192403018 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500404 | GGACAGCAGGGTAGG[A/C]CATACGTCTCCAGCC | 10580 |
rs192403783 | snp | C/T | 0.0102723 | 0.0709268 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356476 | TCAGCTGCTCAAAAG[C/T]GGTGATGCGGGAAGA | 10580 |
rs192406383 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561759 | CTTAGACGTAAAATA[A/G]CAGTGATAAGTTATT | 10580 |
rs192416335 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540850 | CAGGAAGATTAACCC[C/G]TTCCCTGCTGTGCCC | 10580 |
rs192417561 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520661 | AGCTTATAAATGCCT[A/G]AATATACTTCAGCAA | 10580 |
rs192420302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458982 | TAACTTTAGAACTCT[C/T]GGGTTGGTTCCCAAT | 10580 |
rs192430644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535861 | TCCAAACCATGTGTA[G/T]GTATCAAACTATTTT | 10580 |
rs192439765 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314863 | ATTCTTTTTGCTCAG[C/T]ACACTAGTTCGGCCC | 10580 |
rs192522838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484526 | AAACTCTGGCCACTA[C/T]TTTAAAAACTTTTAA | 10580 |
rs192561820 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525054 | AGAAGAGCTAATGCT[A/G]TAGATGCCAGAATCA | 10580 |
rs192582385 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320533 | TACAGGCGCATGCCA[A/C/T]CACGCCCAGCTAATT | 10580 |
rs192593812 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361043 | GATCTCAAACTCCTA[A/T]CCTCAGGTGATCCAC | 10580 |
rs192608280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412317 | TATTGATTAAAATAA[C/G]TCAAATCAATTAACA | 10580 |
rs192615205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433348 | CAGGTCAACTTTTAG[A/G]GTTTCCTTGAGAAAG | 10580 |
rs192632402 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325065 | ATTTCTACTTGGTAG[G/T]GCTGACACTGCTGGT | 10580 |
rs192642887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388104 | CCTGTCACAGCCTCC[C/T]GAGTAGCTGGGACTA | 10580 |
rs192651070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364637 | AAAGTATTTTTTGTA[A/G]AGAGGAAGTTTTGCC | 10580 |
rs192656778 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545626 | AGGCGGAGGCTACAG[A/T]GAGCCAAGATCATGC | 10580 |
rs192669020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495180 | ATGAGCCACCGCACC[C/T]GGTGGTGGTCCTCAA | 10580 |
rs192674750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524435 | ACTACCCCACTGACC[A/G]TACATCACTCCCTCC | 10580 |
rs192674895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475130 | CAGAGACCCAATGAG[A/G]GGGCACAAGCTCAAT | 10580 |
rs192711481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411326 | TTGCTTCTGAGATTT[A/G]GAGATTATCCTATCC | 10580 |
rs192722153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392924 | TCCTTTGCCTGTGTC[C/T]GTGGGATACTGTGCC | 10580 |
rs192759361 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480703 | GTTATGCATCCACTC[A/C]GCAAGCATTTCATGA | 10580 |
rs192761434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438072 | GCTTAGCATTCCATA[A/G]TTAGCACCTCATTTT | 10580 |
rs192763126 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509599 | CCCAAGATTTTCAGA[A/G]AAGACAGGATTTTTC | 10580 |
rs192773847 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405117 | GCACAGAGGGCAGCA[C/T]TGGCATCACCAGGGA | 10580 |
rs192795510 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562693 | GACTGATCGGAAACT[C/T]ATCAGCAAAGATTCT | 10580 |
rs192797697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520881 | TTTCCAAATTAGGGG[A/G]AAGGGTAGTTGGCAG | 10580 |
rs192798200 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320424 | CTCACTCTGTCTCTA[A/G]GCTGGAGTGCAATGG | 10580 |
rs192805805 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468313 | TGGTGACCCTTTCTC[C/G]AAACCGCCCACACTG | 10580 |
rs192817700 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429943 | ATGTATGCTTATTTG[A/G]ATTCGATGATCTCAA | 10580 |
rs192820091 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511618 | TGCAGCCTTTGGGAC[A/T]GAGTTGGAAACTCTC | 10580 |
rs192835361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551183 | GATACAGCCAAGGGA[C/G]GGACACAGCTGAGGG | 10580 |
rs192848541 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342758 | TTTGCTTTTAAACAT[G/T]GAAAAGTGATGTTGG | 10580 |
rs192874908 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555935 | AATTCTTCCTAGATA[A/T]ACTCTCTAGGCCATA | 10580 |
rs192892323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352535 | GCTGTGGGATTTCCA[A/G]TACTCAAATAAGTTG | 10580 |
rs192933870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453143 | ATACAAAAATTAGCC[A/G]GGTGTTGTGGTGCAT | 10580 |
rs192943960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536660 | GCTAAGGCCTGAAGT[C/G]CCTAGACCAGGAGAC | 10580 |
rs192948023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494290 | TGGCAGAAGAAAGGA[C/T]GTGGGAGCATCCAGT | 10580 |
rs192975414 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381628 | CCAACTGCACAATGC[A/T]TTCTGATTAAAGAAC | 10580 |
rs192985545 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429708 | AGGCTTGGAAAGCAT[C/G]TGGCCCAAGTTCCTC | 10580 |
rs192989643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501266 | GCTGAGAAATTGTGA[C/T]CAATATCGGCAAGAC | 10580 |
rs193000666 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541437 | AGACCAGAACCCTTC[A/C]GTGATAAGAAACTGC | 10580 |
rs193018445 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449007 | CACTTGCTATTCCTA[C/G/T]TGAATTCTGACAAGA | 10580 |
rs193025302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533087 | TCTTGGGGGTAATAG[C/T]GCAGGGATCCACCAT | 10580 |
rs193026617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560266 | AAACAAAAATCCAAA[A/G]GCTCGCCCAGAACAT | 10580 |
rs193035126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490498 | CTGGCAGATGAAGGT[A/G]TCTGTGAACATCACA | 10580 |
rs193038557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326797 | ATCCTGTCCAAGATT[A/G]TAGCCAGCAGCCACA | 10580 |
rs193071405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330179 | AGATTCTCAAAGGTT[A/C]TGTGATCCAGAAAAA | 10580 |
rs193106549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406428 | TCTCAAGATGATTCC[A/G]TCATAGAAGGGAATC | 10580 |
rs193126191 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441408 | CATATTTGGTGCTGA[C/T]GTTATCCGACATCCC | 10580 |
rs193131740 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396929 | GAGCTGCTCACATCC[A/C]AGGCAGACAGATGCT | 10580 |
rs193134587 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365892 | AGAAAAATTAACATG[A/G]TGGATCTAGCTAGAG | 10580 |
rs193142505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372336 | AAACTTAAGAAAAGA[C/T]GGGGGGGAAAAAAGA | 10580 |
rs193151490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556776 | GGCTGGTCTTGAACT[C/T]CTGACGTCAGGTGAT | 10580 |
rs193167582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474020 | CTTAGAGAGAAGTGA[A/G]TAACTTCCTGCAATT | 10580 |
rs193174562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432657 | GTTAGCAAATTGTTA[C/T]AGCCGGGGAATGAGA | 10580 |
rs193175406 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516168 | AGTTCTTCAGGTGTG[A/G]TCACCAGCCCAGCAG | 10580 |
rs193192935 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313385 | CTGTAAAGACTCTAG[A/G]CTTTGGGACAATGGT | 10580 |
rs193284517 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504993 | AGGGAGTTTCTAGAG[C/G]AGCAGCTGCCGTCGT | 10580 |
rs193285901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347304 | CTCAATTCCTGCCAT[A/G]GGTGAAGGCCTTTGG | 10580 |
rs193286736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424010 | CAAGGTAGGGTAAAG[G/T]TTCCAAGTGATTGGC | 10580 |
rs193289459 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463526 | GAATTTTTGGTTCTG[C/T]AAATGGAGGCATTAA | 10580 |
rs193300385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537208 | ATCATTCATTACTGC[A/G]TTCATCCAACAAATA | 10580 |
rs193920900 | snp | A/C/G/T | 8.93733e-05 | 0.00668428 | SORBS1 | 10 | allele_origin=G(germline)/C(somatic) | 10:95337020 | ATCGTCCCACCCCAC[A/C/G/T]ATCAGTAGCTTCTCC | 10580 |
rs199509121 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343576 | TAGGTGTGAGCCACC[A/G]CGCCTGGCCCTTATA | 10580 |
rs199511445 | in-del | -/TG | 0.0283406 | 0.115616 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392212 | AGCTCACAGACAACA[-/TG]AAAACCACAAATCAA | 10580 |
rs199523315 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367223 | TTTCCTTTTTTTTTT[-/G]TTGGGTAGAGACAGG | 10580 |
rs199570808 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458648 | AAAAAAAAAAAAAAA[C/T]AAAGAAAAAGAAAAA | 10580 |
rs199576873 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466796 | GGATATCGCAGATTT[C/T]TTTTTTTTTTTTTTT | 10580 |
rs199580193 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371440 | AGTCTGGTTCAAGAA[A/G]GAAAAGATGGGAAAG | 10580 |
rs199593310 | snp | A/G | 4.94254e-05 | 0.00497094 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336752 | ACCAGGGCCTCTTTC[A/G]CCTGCCCCCCTCTCT | 10580 |
rs199599046 | in-del | -/CCA | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402594 | GACTACAGGTGTGCG[-/CCA]CCACATCTGGCTAGT | 10580 |
rs199612434 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319858 | ACACTTTTTTTTTTC[A/C]TGTTTCTGTATTTGC | 10580 |
rs199618678 | in-del | -/CACACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432328 | ACACACACACACACA[-/CACACAC]CCCCCCCCCCCAAGA | 10580 |
rs199626719 | snp | A/G | 0.00299557 | 0.0385851 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410582 | CCCAAGTATCATGGA[A/G]TAGCTATGTTGATTC | 10580 |
rs199652597 | snp | A/C | 0.000148678 | 0.00862073 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341414 | AGGAGGAAGAAGCTG[A/C]GAAAGGGAAAGAGGT | 10580 |
rs199714069 | in-del | -/CA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554618 | GCAGTGAGCTGAGAT[-/CA]TGCCACTGCACTCCA | 10580 |
rs199726762 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399482 | TAAAAAAAAAAAAAA[-/A]GCCTTGCCAACAGTG | 10580 |
rs199741909 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384905 | TTGATTCCACCTCAA[C/T]CTGGTTCCCTGAGTA | 10580 |
rs199760545 | snp | A/G | 0.00020084 | 0.010019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371319 | CATGAGAAAAACTAG[A/G]AAATACCTGTGGCAC | 10580 |
rs199816318 | snp | C/T | 6.74923e-05 | 0.00580875 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336575 | CTCGCCACCTCTATG[C/T]CGCTCTGTCTGCTCA | 10580 |
rs199828388 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501347 | GTGTGACCCACCTGT[G/T]GAGACACCAGGAACT | 10580 |
rs199859199 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367224 | TTTCCTTTTTTTTTT[C/G/T]TGGGTAGAGACAGGG | 10580 |
rs199900255 | in-del | -/C | 0.039522 | 0.134904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447163 | AAACAAACAAACAAA[-/C]AAAAAACAAAAAAAC | 10580 |
rs199918000 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322409 | ATTAAAAAAAAAAAG[C/T]CAGCAGCATAAAAGC | 10580 |
rs199940221 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95421985 | GTCAGAAGGAAGGTT[A/G]GGATGCACACTTCTG | 10580 |
rs199952675 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466372 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 10580 |
rs199989930 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530394 | TCTTTGAAACCTCAG[-/C]CCCCTAGCTCAGCTT | 10580 |
rs199996468 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386256 | TTCAGGTTTTTTTGT[C/T]TTTTTTTTTTAAGCC | 10580 |
rs200004857 | snp | C/G | 3.29946e-05 | 0.00406155 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414707 | GAAGGTCAGAGGTGA[C/G]GCGGCAGAGGCAGTC | 10580 |
rs200032340 | snp | A/C/G | | | missense | SORBS1 | GRCh38.p7 | 10:95339162 | TGGCACTGCGACTTG[A/C/G]GGAGGAGGAGAAAGG | 10580 |
rs200035448 | in-del | -/T | 0.0825414 | 0.185628 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326696 | CTGTTTATCCTCAGG[-/T]TTTTTTTCCCCTCTA | 10580 |
rs200059856 | in-del | -/CCCG | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442523 | ATGTGGCACCCCCCC[-/CCCG]CACCCTTACTTATGC | 10580 |
rs200078157 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367224 | TTCCTTTTTTTTTTT[-/G]TGGGTAGAGACAGGG | 10580 |
rs200081952 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366031 | CAATGTAGGTAGGAT[A/T]TGTCCCAGAGACCAC | 10580 |
rs200085487 | in-del | -/TCTG | 0.0517044 | 0.152246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370153 | GAGATCTGTCTTGGT[-/TCTG]TCTGCTTAAGTGTGG | 10580 |
rs200086011 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444646 | TGGCTGTATTTCATT[G/T]TAATAACACTCCATA | 10580 |
rs200104837 | snp | A/G | 0.000512443 | 0.0159987 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371360 | GGTGCTTTATTAAGC[A/G]TCTCCATTTTTTCTA | 10580 |
rs200113127 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510798 | TGAGACTCTGTCAAA[A/T]ATTTTTAAAGTGGAA | 10580 |
rs200113764 | in-del | -/AAGCA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517524 | CCTTACACTGATTAT[-/AAGCA]AATGTTACCCTCATT | 10580 |
rs200117966 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383923 | CCTAAGAATGGAGGC[C/T]CCTAGGTCTCAATGA | 10580 |
rs200147341 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527128 | TCAGCTCATATGAAA[A/G]AATTTTAACAATTAG | 10580 |
rs200147379 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406455 | AATCCATCCAACCCT[A/C]CAGCTTCAAGTGAGC | 10580 |
rs200149139 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506264 | ATGTGCACACACATA[C/T]ACACACACACACACA | 10580 |
rs200178451 | in-del | -/GGA | 0.0475351 | 0.146656 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406227 | GGCATAACTCGTTAG[-/GGA]GATCTCAACCCTGAG | 10580 |
rs200179325 | snp | A/G | 0.0046269 | 0.0478753 | missense | SORBS1 | GRCh38.p7 | 10:95432480 | TGCCGGGTTTCCTGA[A/G]GGCTCGCAGGGCTAC | 10580 |
rs200192581 | snp | C/T | 0.000399281 | 0.0141238 | missense | SORBS1 | GRCh38.p7 | 10:95381729 | TGCCAGGCTGATATT[C/T]GTAAATGCTCTTGGG | 10580 |
rs200219543 | in-del | -/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476117 | TCACATCATCTCCAG[-/GC]GCCAGATCAGCCCCA | 10580 |
rs200229884 | in-del | -/A | 0.33128 | 0.236418 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552896 | TCTCCAAGCGGGCGT[-/A]AAAAAAAAAAAACAG | 10580 |
rs200259418 | in-del | -/GA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344861 | AAAACACTGAGTTAG[-/GA]GGAAGGAGCCCTCTC | 10580 |
rs200314369 | snp | A/G | 3.3168e-05 | 0.00407221 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95371335 | AAATACCTGTGGCAC[A/G]TTTGCACTGGGTGCT | 10580 |
rs200315862 | snp | A/C | 8.24192e-05 | 0.00641894 | missense | SORBS1 | GRCh38.p7 | 10:95318371 | CAACGATATCTCCAT[A/C]GCGGAGTTCCAACTC | 10580 |
rs200318782 | snp | C/T | 3.32071e-05 | 0.00407461 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434584 | CCATGCCATGATCCG[C/T]TCACAGTTAGAGAAA | 10580 |
rs200324425 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331175 | GAGAAGTGACTCAAC[-/A]AAAGATACTTGGCAA | 10580 |
rs200337020 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434160 | GCTCTGGGATGGCCC[A/C/G]GTGAGCATCAGAGGC | 10580 |
rs200346901 | in-del | -/AGTAGGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419423 | TATGCTGATAATGGC[-/AGTAGGG]AGGTAAGCAAAAGAT | 10580 |
rs200349784 | snp | A/C/T | 8.3029e-05 | 0.00644274 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384204 | CACCACTTTCCCTTC[A/C/T]GCCCCCACAACCAGG | 10580 |
rs200362380 | snp | A/G | 0.000128692 | 0.00802056 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337214 | CTCAGAGGTGACAGC[A/G]TGCATCTCGGGGGAC | 10580 |
rs200376516 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452759 | ACAAACACACATATA[A/C]ACACACACACACACA | 10580 |
rs200384218 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450505 | ACATTTGTGATTACA[-/G]ATTTTTTTTTTTTTT | 10580 |
rs200400589 | in-del | -/GAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509630 | TTCCTCAAAAAAAAA[-/GAAG]AAAAAAAAAAAAAAA | 10580 |
rs200400657 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318059 | ATAAATAAATAAATA[A/T]AAAAAATAAATGGAA | 10580 |
rs200430228 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507908 | GAGCGAGACTCTATC[A/C]AAAAAAAAAAAAAAA | 10580 |
rs200431062 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496649 | TTTAGCTCTCCCTTC[-/A]AAAAAAAAGGAAAAA | 10580 |
rs200440325 | in-del | -/CTCAAC | 0.0475351 | 0.146656 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406231 | ATAACTCGTTAGGAT[-/CTCAAC]CCTGAGTCCTCACTG | 10580 |
rs200450213 | in-del | -/CA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358691 | ACACACACAGACACG[-/CA]CATGCACAGACATGC | 10580 |
rs200470697 | snp | G/T | 8.47465e-05 | 0.00650892 | missense | SORBS1 | GRCh38.p7 | 10:95357792 | ACTGCATGGAAGTTG[G/T]AAGAATATATACTAT | 10580 |
rs200473424 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343257 | ATGAAAAAAGAAGGA[-/T]TAAAAATTATAACCT | 10580 |
rs200477664 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325589 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTT | 10580 |
rs200485588 | snp | C/T | 4.94654e-05 | 0.00497295 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397207 | CACAGCTTCTACAAA[C/T]GAAAATCAGTACCTC | 10580 |
rs200490577 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509630 | TTCCTCAAAAAAAAA[A/G]AAGAAAAAAAAAAAA | 10580 |
rs200518733 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517527 | TTACACTGATTATAA[G/T]GTTACCCTCATTTGC | 10580 |
rs200544242 | snp | A/T | 1.70113e-05 | 0.00291639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381675 | AAAATAACTTTAATA[A/T]GCACATTACCATCTT | 10580 |
rs200552140 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376398 | AATTTTCAGTAATGT[A/G]GAAGAAAAGAAAGCC | 10580 |
rs200603565 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512441 | AAAAAAAAAAAAAAA[C/T]ACCAGGACAGGTCCA | 10580 |
rs200649994 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344862 | AAACACTGAGTTAGG[A/G]GGAAGGAGCCCTCTC | 10580 |
rs200657579 | snp | A/C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373749 | TTTTGTGGCAGAGTG[A/C/G]TTGCAGTAGGAAGTG | 10580 |
rs200673492 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512190 | TAGGAGGCCAAAGCA[-/G]GCAGATTACTTGAGA | 10580 |
rs200673767 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377340 | TCTTCTTGTACTTTA[C/T]TTACAACACAGTTAA | 10580 |
rs200678394 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351807 | CCTACAGCATATTCC[C/T]CTGGCAGGACCAGGG | 10580 |
rs200688441 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554885 | CTCTTTTTTTGTTTG[-/TT]TTTTTTTTTTTTGAG | 10580 |
rs200688569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397317 | AAAGAGCAAAATTAA[A/G]TGACTATCTTGACAC | 10580 |
rs200698975 | in-del | -/TTAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365171 | TTTCATTTACTAACC[-/TTAT]GTGTGTGTGTGTGTG | 10580 |
rs200713070 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513158 | CCTTTGCCTAAGCAG[C/G]AGGGTCAGTTCTGCC | 10580 |
rs200721753 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513331 | GCAAAGAGCCAATCC[-/T]GGCTCCAATCAGCAC | 10580 |
rs200744035 | snp | A/G | 3.43289e-05 | 0.00414286 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315027 | GATGCTTCCTCCTCC[A/G]ATAAAAATAATCTCC | 10580 |
rs200754470 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513326 | ATCCAGCAAAGAGCC[-/A]ATCCTGGCTCCAATC | 10580 |
rs200770302 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314314 | CAAGTGGCCTCCAGA[A/G]CCACAGGGCTTCCTG | 10580 |
rs200770389 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407377 | ACTACACTGAAGGCT[-/G]CTGAGCTCCAGCTGG | 10580 |
rs200781048 | snp | C/T | 0.000575666 | 0.0169559 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371304 | AAAAGGAACTGATGG[C/T]ATGAGAAAAACTAGG | 10580 |
rs200817096 | in-del | -/AAAAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350198 | TAGAAAAATAAATAA[-/AAAAT]AAAATAAAAAAGATA | 10580 |
rs200828108 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357420 | GAAGGAGAACAAGGT[G/T]GGGGGGTCAAAGGAA | 10580 |
rs200834149 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483651 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTATGG | 10580 |
rs200835885 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510811 | AAAATTTTTAAAGTG[C/T]AAAAAAAATGAAAGC | 10580 |
rs200847211 | in-del | -/AT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535533 | TAAGAGGCAAAAGCA[-/AT]ATATATATATTATAC | 10580 |
rs200848696 | in-del | -/GT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560095 | TGGGCGGGGGGGGGG[-/GT]GTTGAGGGGAGAGAT | 10580 |
rs200850782 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445423 | CCAGGGCCTGATTCT[-/G]GCTCTGATCCCAGCC | 10580 |
rs200856746 | in-del | -/GTCA | 0.0162398 | 0.0886349 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386423 | GGTGTATCGCTTGAG[-/GTCA]GGAGTTTGAGACCAG | 10580 |
rs200874517 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510803 | CTCTGTCAAAAATTT[A/T]TAAAGTGGAAAAAAA | 10580 |
rs200880097 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397806 | TTGGAATGGTTGGGC[-/T]TTTTTTTTTAAGATA | 10580 |
rs200902052 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327265 | GCATGCATACACACA[C/T]ACACACACACACACA | 10580 |
rs200903648 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387981 | CTTGCTACATCTTTT[C/T]TTTTTTTTTTTTTTT | 10580 |
rs200903806 | in-del | -/G | 0.0337553 | 0.125452 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447201 | GGTACTGGGTGCCAT[-/G]GCTCGTACCTGCAAT | 10580 |
rs200912166 | snp | C/T | 1.83333e-05 | 0.00302759 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414546 | ACTCTGCGGAGGTCC[C/T]CCGGGGCAGGAGGGA | 10580 |
rs200930260 | in-del | -/A | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312090 | ATGAAATTAAAAAGG[-/A]AAAAAAAAACTGTAA | 10580 |
rs200937112 | snp | A/G | 0.0002636 | 0.0114774 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336873 | TCAGAGCTCCCCAGC[A/G]GCAGCTGCAAGAAGC | 10580 |
rs200947628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509832 | GGGGGCTAACGGTGA[C/T]GGTGTCGGAGACTGC | 10580 |
rs200962705 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516659 | AATAATTAAAAGTTA[A/C]CAGCCCACACCCATT | 10580 |
rs200963181 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95402439 | GCATTTCCTCTTAGT[C/T]TTTTTTTTTTTTTTT | 10580 |
rs200989458 | in-del | -/TATTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342882 | TATTATTATTATTAT[-/TATTA]TTTTTTTTTTTTTTT | 10580 |
rs201012466 | snp | A/T | 0.497359 | 0.0362457 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448269 | TCCAACTACATGCTC[A/T]CTTCTTTAGAACCAG | 10580 |
rs201013572 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562780 | TATTAAAAAAAAAAA[A/G]AAGAGTCCTAGCCAT | 10580 |
rs201055950 | snp | C/T | 0.000214693 | 0.0103586 | missense | SORBS1 | GRCh38.p7 | 10:95422011 | TTCTGTAGCCCTTGG[C/T]AGCGAGTGAAGAGGG | 10580 |
rs201068623 | snp | C/G | 0.00299541 | 0.0385841 | stop-gained | SORBS1 | GRCh38.p7 | 10:95397257 | TTTAAACATAGTCTT[C/G]TACCAGTCTTTTGAT | 10580 |
rs201096818 | in-del | -/CTAAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412099 | ATAACTACACTTTTC[-/CTAAT]TTATCTCCAAAGTGA | 10580 |
rs201100347 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432331 | ACACACACACACACA[-/C]CACCCCCCCCCCCCA | 10580 |
rs201103977 | in-del | -/AAAAAAAAAAA | 0.207559 | 0.246371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494081 | CTTTTAAATAAATGT[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 10580 |
rs201121643 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509633 | CTCAAAAAAAAAGAA[A/G]AAAAAAAAAAAAAAA | 10580 |
rs201168580 | in-del | -/TTC | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425316 | CTGAAATGTGAACTG[-/TTC]TTCTAAATCTCCAGG | 10580 |
rs201169599 | snp | C/G/T | 6.62453e-05 | 0.0057549 | missense | SORBS1 | GRCh38.p7 | 10:95432460 | CACCTGGTTTGCTTT[C/G/T]GTGTTGCCGGGTTTC | 10580 |
rs201192618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354986 | TAAAACAACAAAGTA[C/G]AGTTAAAACAGGCAA | 10580 |
rs201210793 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467672 | TTGAGAGGTGTTTTT[-/G]TTTTTTGGAATAGAA | 10580 |
rs201213066 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419408 | AAAGGGACTGGCGGG[G/T]ATGCTGATAATGGCA | 10580 |
rs201232632 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367225 | TTCCTTTTTTTTTTT[G/T]GGGTAGAGACAGGGT | 10580 |
rs201236157 | snp | A/C | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312180 | ACAATGGCTATTTTT[A/C]TGCTAAAAATCTGTA | 10580 |
rs201243419 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517528 | TACACTGATTATAAT[A/G]TTACCCTCATTTGCT | 10580 |
rs201334060 | snp | G/T | 0.000575333 | 0.016951 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367748 | AAAAATAATGTAGAT[G/T]ATTTATTTTGACTCA | 10580 |
rs201348223 | in-del | -/ATCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406229 | GCATAACTCGTTAGG[-/ATCT]CAACCCTGAGTCCTC | 10580 |
rs201356588 | snp | C/T | 3.48803e-05 | 0.00417599 | missense | SORBS1 | GRCh38.p7 | 10:95339140 | TTAGATACCTGTGGG[C/T]TTGCAGTGGCACTGC | 10580 |
rs201364821 | snp | G/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312981 | ACAAAAAAAAAAAAA[G/T]AGTGCTCTTAGATGG | 10580 |
rs201378885 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95372350 | CGGGGGGGAAAAAAG[-/A]AAAAAAAAAGCATTA | 10580 |
rs201403784 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319857 | AACACTTTTTTTTTT[C/T]ATGTTTCTGTATTTG | 10580 |
rs201418351 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381454 | AGTTAAAACCATGCA[G/T]AAAAAAAGCAACAGA | 10580 |
rs201444487 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373750 | TTTGTGGCAGAGTGG[A/C]TGCAGTAGGAAGTGA | 10580 |
rs201454148 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474840 | TGTTTTAAAGCTATG[-/T]TTACACTCCCTGATA | 10580 |
rs201460914 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447162 | AAAACAAACAAACAA[-/AC]AAAAAAACAAAAAAA | 10580 |
rs201460944 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481648 | CATCAATGCAGGCTG[G/T]TGCCCATGCATGTGA | 10580 |
rs201461385 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501343 | GCAGGTGTGACCCAC[C/T]TGTTGAGACACCAGG | 10580 |
rs201465548 | in-del | -/TAGT/TAGTGA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408838 | CTGATGCTTCCTGCC[-/TAGT/TAGTGA]CCACCTGCTTAGTGA | 10580 |
rs201465567 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330497 | TCCCCCTTACTTTCC[-/T]TTTTTTTTTGTTTAC | 10580 |
rs201529860 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534952 | CACACTGCACCATAT[C/G]TGTCTGTCTCCCGTA | 10580 |
rs201539027 | snp | A/G | 0.000105994 | 0.00727913 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384335 | CTGGCTAAGGTAAGA[A/G]AACCAAGTTGTATGT | 10580 |
rs201550848 | in-del | -/A | 0.0205511 | 0.0992634 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312234 | TTTAAATAAAAATGC[-/A]AAAAAAACTTCATGA | 10580 |
rs201571555 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371445 | GGTTCAAGAAAGAAA[A/G]GATGGGAAAGAAGGT | 10580 |
rs201573146 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325569 | TTTTTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTG | 10580 |
rs201578718 | in-del | -/CA | 0.0189856 | 0.0955633 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369743 | CTCTCACCACAGCCA[-/CA]GTCACCATTCTCACT | 10580 |
rs201580766 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343053 | AATTTTGTGTGTGTG[-/T]TTTTTTTAGTAGAGA | 10580 |
rs201602204 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407946 | GTGAGACCTTGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 10580 |
rs201624610 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432341 | ACACACACCCCCCCC[-/A]CCCCAAGAGGTATCT | 10580 |
rs201632885 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406226 | TGGCATAACTCGTTA[-/G]GGATCTCAACCCTGA | 10580 |
rs201634596 | snp | C/T | 6.63361e-05 | 0.00575879 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341558 | AAAGAAAAGAGGCTG[C/T]GGTACCTCGATGTAG | 10580 |
rs201646270 | snp | C/T | | | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414729 | GAGGCAGTCGCTGGG[C/T]TTGTGGGGACGCAGC | 10580 |
rs201656325 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349846 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTTGCT | 10580 |
rs201656698 | snp | G/T | 1.71873e-05 | 0.00293144 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422086 | CATCTGAGAAATAGA[G/T]AGGAAAAAATCTCTC | 10580 |
rs201679559 | snp | A/G | 1.799e-05 | 0.00299911 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337057 | AACTCAAATGGGGGA[A/G]GCTGAGAGACAGGGA | 10580 |
rs201697009 | in-del | -/TA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365172 | TTCATTTACTAACCT[-/TA]TGTGTGTGTGTGTGT | 10580 |
rs201713862 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408589 | AAAAGGGGGGGGGGG[-/A]GCAGGGAGGGAGGCA | 10580 |
rs201724950 | snp | A/C | 1.65616e-05 | 0.00287759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322699 | AAGTAAGGATCAGTA[A/C]AAATTCTCTTTAGAA | 10580 |
rs201740072 | in-del | -/TG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364430 | AATAGTTGCTTAAAT[-/TG]TGTGTGTGTGGGGGG | 10580 |
rs201751528 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342887 | ATTATTATTATTTTT[A/T]TTTTTTTTTTTGAGA | 10580 |
rs201793009 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502985 | TGCTTACACACATAC[A/G]CATACACACACAAAC | 10580 |
rs201794958 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404499 | TGTTTACACGTGTGG[C/T]TTTTTTTTTTTTTTT | 10580 |
rs201812750 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418092 | CTTTTTTTTTTTTTT[C/T]CCCGAGATGCAGTCT | 10580 |
rs201818374 | snp | C/T | 0.000148487 | 0.00861518 | utr-variant-5-prime | SORBS1 | GRCh38.p7 | 10:95441169 | CGTCTGCAACTGGGG[C/T]TCTGAACTGCTCTGT | 10580 |
rs201835257 | snp | C/G | 0.497359 | 0.0362457 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448270 | CCAACTACATGCTCA[C/G]TTCTTTAGAACCAGA | 10580 |
rs201853769 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453925 | TATATGAAACACTGT[-/A]AAATTGTTGTGTTAT | 10580 |
rs201854321 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379388 | TATCTCAACAAAAAA[-/C]AAAAAAAAAAAAAAA | 10580 |
rs201897851 | snp | C/G | | | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414849 | GGCTGGGCTGCACTG[C/G]AGGAAGTGGCATCCT | 10580 |
rs201902636 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377859 | TTTTTTTTTTTTTTT[C/T]TTAAATAAAATGTAC | 10580 |
rs201907208 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415112 | ACACTTTATGAGAGA[A/G]AAAGAACAGAACAGG | 10580 |
rs201912861 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385081 | TGACACACATTCCTA[C/G/T]GTAGGCTAGACACTG | 10580 |
rs201934727 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517528 | ACACTGATTATAATG[-/A]TTACCCTCATTTGCT | 10580 |
rs201957196 | in-del | -/AAG | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362928 | TAATTTAGTTATTTC[-/AAG]AAGAAGAAGAAGAAG | 10580 |
rs201961192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457904 | TCATGAGGCCAAAGG[C/T]CTCAGAGCATCATAG | 10580 |
rs201965496 | snp | C/T | 4.94491e-05 | 0.00497213 | missense | SORBS1 | GRCh38.p7 | 10:95381735 | GCTGATATTCGTAAA[C/T]GCTCTTGGGCTCTGC | 10580 |
rs201973683 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395114 | AGAGAGAATAGAGGA[A/G]GATACAAATGGAGAG | 10580 |
rs202003127 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502994 | ACATACACATACACA[A/C]ACAAACACACACACA | 10580 |
rs202027050 | in-del | -/AAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405454 | CTGTATCAAAAAAAA[-/AAAG]AAAAGAAAAGAAAAG | 10580 |
rs202046171 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545697 | TGAAAAAAAAAAAAA[C/T]GGGAGAGAAACAAAG | 10580 |
rs202075782 | snp | C/T | 4.94637e-05 | 0.00497287 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351354 | TGCTCGCGTTTAAGT[C/T]GTCTCTGGTCCGCTA | 10580 |
rs202077410 | snp | C/T | 1.6504e-05 | 0.00287258 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395075 | TTTTCTTCAGGAGTG[C/T]CTAGGCAGAGGAGCA | 10580 |
rs202097631 | snp | C/T | 0.000105626 | 0.0072665 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95367676 | CTCTGAAGAAATTTC[C/T]GGAGTAGGGCTGATG | 10580 |
rs202097961 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493819 | AACCCCCTATGTACC[A/C]CAGCCATTAAATCAA | 10580 |
rs202100781 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555070 | GTACTTTTAGTAGAG[-/A]GGAGGTTTCACCATG | 10580 |
rs202125191 | snp | A/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442096 | CAGGTCCCTGTTAAC[A/G]ACTGATCTGCTTTCT | 10580 |
rs202129973 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380087 | CTTTGCAATCCATGT[-/AC]GTGCTCACCACCATT | 10580 |
rs202137179 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357279 | GCAAGGATGCAACAA[-/C]AAAAAAAAATGGCTA | 10580 |
rs202141226 | snp | A/G | 0.000131837 | 0.00811795 | missense | SORBS1 | GRCh38.p7 | 10:95384039 | AGGGGTAGTGTGGCC[A/G]ACCTCTTGACTACCT | 10580 |
rs202172843 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485764 | AAAAAGAAAAAAAAA[-/A]GGAAAGACAAAAAAT | 10580 |
rs202184760 | snp | C/T | 0.000122362 | 0.00782086 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356781 | TAATCCCGTCGGGAG[C/T]GCATGAGCAGGTTCT | 10580 |
rs202215002 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318022 | AGTGAGATTCTGTCT[A/C]AATAAATAAATAAAT | 10580 |
rs202232411 | snp | C/G | 0.000149619 | 0.00864797 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337223 | GACAGCGTGCATCTC[C/G]GGGGACAGGGCTCGG | 10580 |
rs202235557 | snp | G/T | 6.71321e-05 | 0.00579323 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354879 | TTAAAAGATGGGATT[G/T]ACCTCTTTATCATCA | 10580 |
rs202242382 | in-del | -/AG | 0.0962929 | 0.197165 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328208 | TGGGCAAACTCTTCC[-/AG]AGGAGTAGAAAGGCC | 10580 |
rs207471282 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527399 | CCACTGCACCCCAGC[A/C]TGAGCAACGGGGTGA | 10580 |
rs267602646 | snp | A/G | | | missense | SORBS1 | GRCh38.p7 | 10:95339270 | GTCGGGATGTCCCCG[A/G]GATCCTCCCTTCGTA | 10580 |
rs367575321 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535099 | GAGAGATGGATGGAT[A/G]AGTAGATGGATACAG | 10580 |
rs367589260 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457856 | TCAAAAAAACAAGAA[C/G]AAAAACAAGGCAATA | 10580 |
rs367590257 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522305 | TGAGTCCCTACTTAA[C/T]ATATGCATGTTTCCC | 10580 |
rs367623985 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476357 | GGTGAAATATTTGAG[C/G]AACATTGTTCAGTCC | 10580 |
rs367637788 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558970 | CCACTAGCCCAAAGC[C/T]CAAAGATTGGTGGCC | 10580 |
rs367645756 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428866 | TATCTGCAAAGGCAT[C/T]GGGAGTAGGAAGCAA | 10580 |
rs367645932 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378769 | TGTGTGTGTGTATGT[A/G]TGTATGTATATATTT | 10580 |
rs367666306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364988 | AATGGGGATTAAAAA[C/T]AATGCCTCATCTTGG | 10580 |
rs367675991 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320464 | GGTTCACTGCAACCT[A/C]CGTCTCGGGAGTTCA | 10580 |
rs367690122 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | SORBS1 | GRCh38.p7 | 10:95432540 | GCCCGGAGAGTCACC[A/G]CTCCCTTCCCAGTGC | 10580 |
rs367727847 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360110 | AAAAATAAATATGTC[C/T]CTTTTCTAAATTTCC | 10580 |
rs367748572 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380872 | AATAAAAACCAAACT[C/G]CAGCATAATAATTCC | 10580 |
rs367784194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456759 | AATACGCCTCAACCA[C/T]ATATACCCTCTCTGC | 10580 |
rs367800903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544017 | GAACATGACGCTCCA[A/G]GTGAGATCTGAGGGG | 10580 |
rs367801772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458130 | AATGTCCAGGTACAC[A/G]TCCTCCCTAAAACAA | 10580 |
rs367808639 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95550474 | TAACACTGTCTCCCT[C/G]CCAGTGCGTCTTATC | 10580 |
rs367822713 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346293 | ACTACTGTTTTGTTC[-/T]TTTTTTTTTAACAAC | 10580 |
rs367837785 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446822 | AGGGAGCCAGCTCCC[C/T]ACTTGAACAAAATGC | 10580 |
rs367843767 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474263 | GAACCAGCACCACCA[C/T]TGTGTGGCTGAAATA | 10580 |
rs367846974 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441948 | ATATAACCAAAAATA[C/T]CCATTTTAATTGTAC | 10580 |
rs367873234 | snp | A/G | | | missense | SORBS1 | GRCh38.p7 | 10:95318415 | GGTATATAGCTATAT[A/G]ATGCTTGATAGCTAA | 10580 |
rs367941968 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455873 | CCTGGGTGGTCGAGG[C/T]TGCAGTGAGCCATGA | 10580 |
rs367958444 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318779 | CTTTTAGGCACCAGG[A/G]ACTGGTTTTGTGGGA | 10580 |
rs367958629 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425923 | AATGTTACCTTAGAG[A/C]TCCCAAGCTGGGGGG | 10580 |
rs367969159 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458848 | GACAGAGGGCATGTT[A/T]AGAAGACTATAGAGA | 10580 |
rs367985659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548245 | CCTGGCTGAGAAACA[C/T]TCCATTACGTATCCC | 10580 |
rs368012565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444376 | TGCAGGGATTATAGG[C/T]GTGAGCTACTGCACC | 10580 |
rs368019203 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537861 | TGGTGGCTCACACCT[A/G]TAATCCCAGCATTCT | 10580 |
rs368021159 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531034 | AGGCAACTACCAGCT[C/T]GCAGCCAGGTAGAGC | 10580 |
rs368027431 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549408 | CGCTGGTCTATAACC[A/G]GTGCTCAATAACTAT | 10580 |
rs368066700 | in-del | -/CACACC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432330 | ACACACACACACACA[-/CACACC]CCCCCCCCCCAAGAG | 10580 |
rs368091539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392006 | CAGATTTCTCAGTAA[C/T]GCTGTTTCTTAATGC | 10580 |
rs368100630 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335858 | TCAAAACACCCTAAG[G/T]CTACCTTTGTCCAAA | 10580 |
rs368147154 | snp | A/C | 6.58989e-05 | 0.00573978 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336762 | CTTTCGCCTGCCCCC[A/C]TCTCTGCTTTCCTCT | 10580 |
rs368152127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333231 | TCTCCGAGGCTGCTA[C/T]CTGTGAGCTTTCATC | 10580 |
rs368160259 | snp | C/T | 1.66726e-05 | 0.00288722 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432593 | TGAAAAGAAAAGGTC[C/T]AAAATTGAAGACTGA | 10580 |
rs368164916 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324101 | CCTCCCCTGAGGTCA[C/T]ACATCAAGTCAGTGG | 10580 |
rs368175316 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375833 | AGGTTGTAGTGAGAA[C/G]AGACAATCCCACTAC | 10580 |
rs368176187 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563365 | ACGCCTGTAATCCCA[A/G]CACTCTAGGAGGCCA | 10580 |
rs368178049 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519192 | ACATCAGAAAGCCAA[A/C]AAACCCAACAGCCAA | 10580 |
rs368184745 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549976 | GCCCTCAACAAGCTA[C/G]GCTTGTTCTCCAAGC | 10580 |
rs368193039 | snp | A/G | 3.29848e-05 | 0.00406095 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384272 | TCTGGGAGAGTACAG[A/G]TCTGAATCATCATCT | 10580 |
rs368221457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474557 | GAAATTTGGAGGACA[A/G]AATGTCCTGTTGTCC | 10580 |
rs368222290 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447511 | GGACTTGATTTTATA[C/T]ACGTACAGCTACTTC | 10580 |
rs368234479 | snp | A/G | 0.000149941 | 0.00865726 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383975 | GAATGAGAGACAAGC[A/G]GGCACTTACCTTTCT | 10580 |
rs368239052 | snp | A/G | 3.29663e-05 | 0.00405981 | missense | SORBS1 | GRCh38.p7 | 10:95432502 | CAGGGCTACTGCTTG[A/G]GGTTTCCCTGTAGGA | 10580 |
rs368273763 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397866 | TGGCTAGATATTTTC[A/T]CTCCCACTTTACAGA | 10580 |
rs368282014 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525096 | ACCTTAACAGCCCAG[C/T]ATTCTGGGCGAAAAA | 10580 |
rs368290231 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436930 | CTGTGCAGCCACACT[A/G]AGGTCAGGATGAAAG | 10580 |
rs368299421 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440967 | AACCATGAAGGTGAT[A/G]AGAGTGATGATGACA | 10580 |
rs368300139 | snp | C/G/T | 0.000185649 | 0.00963277 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415603 | CCAGGGAAGGACTCT[C/G/T]GCCACGGTTAACGGC | 10580 |
rs368364820 | in-del | -/CT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534956 | TGCACCATATCTGTC[-/CT]TSTSTCCCGTAGCAA | 10580 |
rs368378806 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537842 | AAGCCAAAAGAGGCC[A/G]GTGTGGTGGCTCACA | 10580 |
rs368398879 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441099 | CAGTTTGGTAGATAA[A/G]AGAAAGATGAGTTTA | 10580 |
rs368402516 | snp | A/G | 5.27876e-05 | 0.00513722 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337165 | TCAGGGCCAGAGAAC[A/G]CCTGCCTGGGACCCC | 10580 |
rs368410760 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430735 | TTGGAAGTGGGTCGT[C/T]CCAGTTAGGCTTGGA | 10580 |
rs368416628 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336538 | GGCTCCCACCTCTCC[A/G]AGCAGCTTTCCTCCC | 10580 |
rs368422382 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465373 | CTCTACTAAAAATAC[A/T]AAAAATTAGCCGGAT | 10580 |
rs368426395 | snp | C/T | 0.00195503 | 0.0312041 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421920 | ACTCAAGAACAGGTA[C/T]CACTCACCAGTCCCC | 10580 |
rs368446819 | snp | A/C/G/T | 7.34789e-05 | 0.00606097 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414537 | GGCTCCGAGACTCTG[A/C/G/T]GGAGGTCCTCCGGGG | 10580 |
rs368461333 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404726 | GTAACAGGAATGCAC[A/G]TCTATTAAGTCATGC | 10580 |
rs368472591 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452322 | GAACACATATATACA[C/G]GCCCAAAATCAATAA | 10580 |
rs368486635 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383370 | GCAGTGAGCCGAGAT[C/T]ACACCACTGTACTCC | 10580 |
rs368515142 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536297 | TCTTTCCTGACATCA[A/G]GCACATTCATAACCT | 10580 |
rs368539280 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563002 | AGTATTTATTGAGCA[C/T]GTCTAGGCTGCTATG | 10580 |
rs368558644 | snp | G/T | 1.64993e-05 | 0.00287218 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357658 | CAGAGCTGGATGGTC[G/T]CTTGAGCCCACTCAG | 10580 |
rs368568316 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344985 | TTGTTTTAAGACTCT[-/TT]ATGAAATCTGGGAAA | 10580 |
rs368577116 | snp | C/G | 0.000251901 | 0.0112199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414364 | ACAGGGGACACGGCT[C/G]CAGTCATCACACAGG | 10580 |
rs368595600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479017 | ACACCCTTCTCACTC[A/G]GTGACCTGTGACTGC | 10580 |
rs368606201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454651 | AAAACAAAGACAAAC[A/G]GATCCTCTTTGGGTG | 10580 |
rs368633657 | snp | A/G | 1.70921e-05 | 0.00292331 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371279 | AAAGAAGAAAACAAA[A/G]CACAGCTTGAAAAGG | 10580 |
rs368635220 | snp | C/G/T | 0.000482276 | 0.0155211 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356187 | GTGGAGATATTTGAA[C/G/T]AGCGGTCCACGTCAT | 10580 |
rs368646007 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539097 | CAGTGACAAACCCAA[A/C]CTATAAATATTCAGT | 10580 |
rs368656423 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501817 | CTTTTTTTCTGCCTT[C/T]GACTGGTACTCTTGC | 10580 |
rs368670354 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457816 | CTTGGCTGTCTGCTA[A/C]ACAGGCCAGTAATTG | 10580 |
rs368675032 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508912 | AGAGACAAAGGGCAG[C/G]AGGTGGGAGTTATTC | 10580 |
rs368680185 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466440 | CAAGACTCCATCTCC[-/A]AAAAAAAAAAAAAGA | 10580 |
rs368702232 | snp | A/C/T | 3.35724e-05 | 0.00409698 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341268 | CCCCAAAGCAAGGCA[A/C/T]GAGAAGTGCAGCTTA | 10580 |
rs368708543 | snp | A/G | 1.79884e-05 | 0.00299898 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337054 | ACCAACTCAAATGGG[A/G]GAGGCTGAGAGACAG | 10580 |
rs368708814 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417342 | GAATCTCGCTCTGTC[A/T]CCCAGGCGGGACTGC | 10580 |
rs368725161 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340752 | TCTTCAGTAGAGATG[A/G]GGCCTTGCTACGTTG | 10580 |
rs368741028 | snp | C/T | 6.59e-05 | 0.00573983 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351290 | GATAAACTGATGGTG[C/T]GTCGGAATGACGCCT | 10580 |
rs368752381 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390157 | GAGGTGGTGTCTTGA[G/T]TGACATCACCGAGAG | 10580 |
rs368757958 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337473 | TACATCTGGGGAGAA[A/G]CCAGGATGGGTGAGT | 10580 |
rs368759044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547558 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 10580 |
rs368762169 | in-del | -/TA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494855 | TCCTCAATTTTTATT[-/TA]TTTATTTATTTATTT | 10580 |
rs368776285 | snp | A/C | 3.35942e-05 | 0.00409829 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432619 | ACTGAATCCAAGACT[A/C]CTGAAGGATTAAAGG | 10580 |
rs368810598 | snp | G/T | 4.9717e-05 | 0.00498558 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406175 | AACACACAGTGTAAG[G/T]AAGATTTATACAGCA | 10580 |
rs368828457 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526420 | TATAGTTTTGAAAGC[A/G]CCCCCCTCTCTCAGG | 10580 |
rs368849029 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436729 | AGCAGAAATAAATAC[A/G]GCAGATCATAAATTC | 10580 |
rs368862305 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469796 | TCTTAGACCCTCAGT[C/G]CCCTGCTCTTATCAC | 10580 |
rs368865818 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493714 | ATTCACCTGAAGAAT[C/T]GGAAGAGCTTCCCTG | 10580 |
rs368941503 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396142 | GCAGCGATGGGAGCC[A/G]GTGGGGTCATGTCCT | 10580 |
rs368959055 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342540 | GGGTGCAAGTGATCC[A/T]CCTACCTCAGCCTCC | 10580 |
rs368977672 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379264 | GCGTGCCTGTAGCCC[C/G]AGCTACTTGGGAGGC | 10580 |
rs368999943 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382486 | TCAGTAATTGATTTT[C/G]GTTTGATTTTTGTAT | 10580 |
rs369003826 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498915 | TACATATAACACAAA[C/T]GATATCTGAATAAGA | 10580 |
rs369011949 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455108 | TAGATGTGTCTTCTG[C/T]GGTTAGTCAGTTAAC | 10580 |
rs369012606 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336855 | AGCTGGGAGATGACA[C/T]TATCAGAGCTCCCCA | 10580 |
rs369022843 | snp | C/G | 4.96249e-05 | 0.00498096 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434603 | CAGTTAGAGAAAATC[C/G]ACCGACCCAAGGAGA | 10580 |
rs369026056 | snp | A/C | 4.94311e-05 | 0.00497123 | missense | SORBS1 | GRCh38.p7 | 10:95399038 | TGGGATGCCCACTTC[A/C]TCCATGGAAACATCG | 10580 |
rs369029685 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332006 | TCATGTATCATGACC[C/T]ATGTGGCCAGTATGG | 10580 |
rs369035134 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551199 | GGACACAGCTGAGGG[A/T]GGTAGAGAGATGGGA | 10580 |
rs369042426 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367898 | GCTCTTTCTCTGGAA[A/G]GAGAATGTATGGGCA | 10580 |
rs369056155 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392753 | TGGTGGCTGATGACA[A/C]AGGAGCTCTGGCTGT | 10580 |
rs369065159 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408840 | TGATGCTTCCTGCCC[A/C]ACCTGCTTAGTGAAC | 10580 |
rs369087273 | in-del | AA/C | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312970 | CAACAACAACAACAA[AA/C]AAAAAAAAACAGTGC | 10580 |
rs369102538 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475933 | GCCAGGATTTGAAAC[C/T]TAAGTCTATGTGACT | 10580 |
rs369104462 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322958 | ACCAAGTCTCCACAA[A/C]AACAGGGTGGGTGCA | 10580 |
rs369113639 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398809 | ATTTACTTGACCACG[A/G]AACCCTTTATTCATA | 10580 |
rs369141762 | in-del | -/TTCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467884 | TCAACCTTTACCATC[-/TTCT]TTTTTTTTTTTTTTT | 10580 |
rs369142661 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489167 | GGCCTTTCTTTTCAC[C/T]TGCTATTCCCTCTGC | 10580 |
rs369167272 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382752 | TTTTTATTTGTGCAT[C/T]ACCGTACTTTGCACT | 10580 |
rs369175277 | snp | A/G | 4.96249e-05 | 0.00498096 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394968 | ATTAATTTAAAGCTC[A/G]GACAACAGATATGCT | 10580 |
rs369180276 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417265 | ATTAGACTATGAGAT[A/G]AGGAAACTGCATTTT | 10580 |
rs369188791 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545039 | GGCCCTGCAAAGCAA[-/A]CACAAAATAGTCCTA | 10580 |
rs369218849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450213 | ACACACCAAGAGCTA[C/T]GCACCTCGTATCCCT | 10580 |
rs369220967 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533809 | ATGACTGGCCGTCCC[A/G]CTCTCCCGGTGGCCA | 10580 |
rs369222511 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409230 | GAACTAACTTAATTC[G/T]GTTTGACTGAATTTT | 10580 |
rs369225741 | snp | A/G | | | utr-variant-5-prime | SORBS1 | GRCh38.p7 | 10:95491096 | GCAGAAAGCTTTCAC[A/G]AACTCTTCCAAAGGA | 10580 |
rs369235706 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440123 | CTAAATCCCAATGAA[C/G]TGGTGTTTTTATTAT | 10580 |
rs369248570 | in-del | -/ACAGACAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392292 | AAAAAACCTCAAAAC[-/ACAGACAA]CAAAAACCCTGTGAT | 10580 |
rs369255356 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370276 | TTTTTTTTCCTGAGA[C/T]GGAGTCTCGCTCTGT | 10580 |
rs369258399 | snp | A/G | 6.62581e-05 | 0.0057554 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95375974 | GCTATTAAACTTACC[A/G]GTTTCCCAAACTCCA | 10580 |
rs369302358 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409229 | GGAACTAACTTAATT[A/C]TGTTTGACTGAATTT | 10580 |
rs369308417 | in-del | -/GCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519187 | ACGACACATCAGAAA[-/GCC]AAAAAACCCAACAGC | 10580 |
rs369311289 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548800 | TCATCTAATCCTCCC[C/T]GCAATCCTGTGAGAT | 10580 |
rs369316232 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328961 | TTACAAATGAGAAAA[C/T]GAAGACCTGCCGTGT | 10580 |
rs369319867 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320173 | CTCTTGCCAATCCTG[A/G]TGCCCCACGCTCAGC | 10580 |
rs369323498 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479402 | TCATCTTCTTACTTT[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs369356614 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412386 | GATGGAGCAGGCATC[A/G]GCTCACAGCTCAGAC | 10580 |
rs369398086 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409841 | TTGTAAAGACAAAGT[C/T]TATTCCTGTATGGAA | 10580 |
rs369400745 | snp | C/G | 1.65872e-05 | 0.00287981 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346500 | AGGATTCATGGACAA[C/G]AAGGACACATTTTCA | 10580 |
rs369402483 | in-del | -/AG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357378 | GAGAGAAAGAGAGAA[-/AG]AGAGAGAGAGAGAGA | 10580 |
rs369410495 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410785 | CTGGAATCCTGAAAC[A/G]AACAAACAAACAATG | 10580 |
rs369424316 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464457 | CTCCTCTCATGTGGT[C/T]ACTACAAGGCTTGAT | 10580 |
rs369441783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513320 | CTTTCGATCCAGCAA[A/G]GAGCCAATCCTGGCT | 10580 |
rs369444305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531639 | ATGGAGAAGCAGCAC[A/G]GACTTTCAACGAGGC | 10580 |
rs369451154 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556318 | CATTTGCCTCTTTTT[C/T]GTTTTGTGTGTAAAA | 10580 |
rs369459252 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503577 | GAACTTCTAAAATAG[C/T]TCTGCTTGTACAAAT | 10580 |
rs369483442 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505693 | TATATTATTACTTAA[C/T]AAACATGGTGTTGGG | 10580 |
rs369493980 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466163 | AAAAAAAATTCTGGC[C/G/T]GGGCACAGCGGCTCA | 10580 |
rs369494460 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351291 | ATAAACTGATGGTGC[A/G]TCGGAATGACGCCTG | 10580 |
rs369497127 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337960 | AGCCCTGGGTCAGCC[C/T]GTTTAATGCTTTCTG | 10580 |
rs369551977 | snp | A/C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529485 | GTTGAAATCTTGTAG[A/C/T]CCAGAGGTCCCAAAA | 10580 |
rs369556686 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312886 | ATACAGTCCACAATC[A/G]GTGAAATGCTGCCGT | 10580 |
rs369562708 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325893 | TGGGAAGCATCTTCA[A/G]GTTCTCCAAACCCCT | 10580 |
rs369564009 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358782 | ATGACTCCTATCCCG[C/T]AGAACCACATAGGCT | 10580 |
rs369571000 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477341 | CCTGCCCTGGGTGGG[A/G]GTCCTGAAGAGCTGG | 10580 |
rs369581328 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378967 | CCCACATACGTGCCA[G/T]GTTTGGTCGCTCAAG | 10580 |
rs369586237 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455478 | GACATGTCCGGTCTT[C/T]CCCCAAGAGCACAAT | 10580 |
rs369600738 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389817 | CCAGTCAATGCCTTT[G/T]GCACTTGCTAGGCGG | 10580 |
rs369609514 | snp | A/T | 0.000153988 | 0.00877328 | missense | SORBS1 | GRCh38.p7 | 10:95341352 | ATAGCTTCTCCATAT[A/T]CCAAAACCTGCACTG | 10580 |
rs369609638 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476999 | GACTCAGTCATCCCA[A/G]AATAGGATGGGTGAC | 10580 |
rs369614220 | snp | C/G | 0.000153988 | 0.00877328 | missense | SORBS1 | GRCh38.p7 | 10:95399129 | GCCTTGCCAGGTGAG[C/G]TGGGTTTTTCCTGGG | 10580 |
rs369617126 | snp | A/C/T | 0.000233849 | 0.0108111 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422222 | GGCTCCAGACCTACA[A/C/T]GTGGTGCAGAAAGGA | 10580 |
rs369657456 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551095 | GTCCCTCTTGCAGTC[C/T]GCTCAGCCTGGTGAT | 10580 |
rs369664153 | snp | A/G | 0.000871284 | 0.0208538 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318445 | AATCTATACATGAAA[A/G]AAATGAATAGTAAGT | 10580 |
rs369692010 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454788 | CCCTTGAAACCCTGA[A/T]GAGCCACTACAAACA | 10580 |
rs369697291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552119 | AAAAAGGCACACACC[A/G]GCTGGACGCAGTGGC | 10580 |
rs369701920 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465389 | AAAAATTAGCCGGAT[A/G]TGGTGGCGAGTGCCT | 10580 |
rs369764260 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415122 | AGAGAGAAAGAACAG[A/C]ACAGGCAGGCAGGCT | 10580 |
rs369796339 | snp | A/G | 1.68105e-05 | 0.00289914 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372094 | AATGAGCATAAAGAC[A/G]TAAAGACAAACATGG | 10580 |
rs369828372 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413789 | CCACCCACAGGATGG[A/G]ACCTGAGGCAGCAGG | 10580 |
rs369836278 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486779 | TATAAACATAACACA[A/C]AAAAAAATTTTAAGT | 10580 |
rs369853316 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487559 | CACATAGGCAGTCGG[A/G]GGAGGAGGCAAATAG | 10580 |
rs369857224 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431146 | TGCATACCCTACTGC[C/G]TAGCCTCTCTGGTCC | 10580 |
rs369862128 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403837 | AGTGCTGGGATTACA[A/G]GCATGAACCACTGCG | 10580 |
rs369865369 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500254 | GTTACACAAAAAGAT[C/G]ACCTGGGGCTCCAGC | 10580 |
rs369868471 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421753 | TTCCAACACCCTGGT[A/T]CAGACCAACCTCATT | 10580 |
rs369883832 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333752 | GCCTGGGTGACAGAG[G/T]GAGACCCTGTCTCAA | 10580 |
rs369910623 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513331 | GCAAAGAGCCAATCC[G/T]GGCTCCAATCAGCAC | 10580 |
rs369926566 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416577 | AGCCCCCAACTCCCT[C/G]TCAAACCTCCTTCCC | 10580 |
rs369927261 | snp | A/G | 6.82047e-05 | 0.00583932 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432413 | TCCCGCCCTTCCCAC[A/G]TGGCTTTGAACAGCT | 10580 |
rs369957615 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385664 | CTTGGCCCACATAAG[A/G]GACAGGCATCGGGTA | 10580 |
rs369963635 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341006 | CTACCATGCCCAGCT[A/G]ATTTTTGTATTTTTA | 10580 |
rs369989818 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318925 | TCACAATAGGGTTCA[C/T]GCTCCTGTGAGAATC | 10580 |
rs369991270 | snp | C/T | 4.96331e-05 | 0.00498138 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95375994 | CCCAAACTCCAATTC[C/T]GAAAAGAATTTATAC | 10580 |
rs370019660 | snp | C/T | 0.00013187 | 0.00811895 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95322786 | AGATCTGGTCCTGCT[C/T]TCAATGAATGATGAG | 10580 |
rs370024746 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481134 | CCTCAACAACTCCCT[A/G]TATGGCCACATCAGG | 10580 |
rs370028123 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314444 | GCAGTCAATGGCACT[A/G]CTGCACAGCAGGCTG | 10580 |
rs370033948 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523186 | AGACTGGGTTTCAAA[G/T]AAGCAATCTGCACTA | 10580 |
rs370034970 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404063 | CTCTGCATCTCCTAA[C/T]GTATGGCTGGAGGCC | 10580 |
rs370036881 | snp | C/T | 3.35801e-05 | 0.00409743 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398973 | GTACACTTGTCACAG[C/T]TTAAGATGAAGCCTA | 10580 |
rs370040263 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502557 | ATTCTACTGCCTCAC[C/T]ATCCTCTGTTCTATG | 10580 |
rs370044372 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513135 | GGAAAGAAATCACCC[A/G]TAAGTCACCTTTGCC | 10580 |
rs370045891 | in-del | -/AGAGCTGGGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467317 | GCTCATGGCTTGGGG[-/AGAGCTGGGG]TTTTCAGCAGTTAGG | 10580 |
rs370054070 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343537 | GTGATCCGCCCGCCT[C/T]GGACTCCCAAAGTGC | 10580 |
rs370069117 | snp | C/T | 3.76925e-05 | 0.00434106 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414466 | GACATTCAGAAAAGC[C/T]GTGAGGAGGGGAGTC | 10580 |
rs370084566 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548153 | CTTATTCAGAGGACC[A/G]GTGACCAGTTGTGAC | 10580 |
rs370097624 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390633 | TCCTAACTATATATT[-/C]TTTTTTTTTTTTTTT | 10580 |
rs370111828 | snp | A/G | 6.65779e-05 | 0.00576927 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376072 | CTATAGGGGTTGGTG[A/G]TAGAGAAATGGAAGA | 10580 |
rs370116176 | in-del | -/AAAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405468 | AAAAGAAAAGAAAAG[-/AAAAG]GGAAGAAAAAGAAAT | 10580 |
rs370122727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445758 | GCAGTGAGGACGCAT[A/C]CATGAAACTACACAA | 10580 |
rs370127278 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432331 | CACACACACACACAC[-/A]CACCCCCCCCCCCCA | 10580 |
rs370137042 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472640 | CTAGTGATTTTAACC[A/G]TTACATCCTACCGAC | 10580 |
rs370139459 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446590 | TGCTCCAGCTTCTCC[C/T]ATGCACTATGGTGTT | 10580 |
rs370151292 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471289 | ATTCATTGAACATTT[-/G]GTTAACATTTAAGGT | 10580 |
rs370161620 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492419 | GAAGTATGCAAGGTG[A/G]TGGAGATACAAAAGT | 10580 |
rs370168951 | snp | A/G | 3.29951e-05 | 0.00406159 | utr-variant-5-prime | SORBS1 | GRCh38.p7 | 10:95441146 | CTCATGGTGGTGGCA[A/G]GACAAGTCGTCTGCA | 10580 |
rs370179222 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321944 | AACATGAGAATCGAA[A/G]TTCACCAGGAGTACT | 10580 |
rs370181498 | snp | A/G | 0.000115368 | 0.00759412 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351346 | CCTCTTCTTGCTCGC[A/G]TTTAAGTCGTCTCTG | 10580 |
rs370214910 | snp | A/G | 3.29853e-05 | 0.00406098 | missense | SORBS1 | GRCh38.p7 | 10:95339236 | ATCACATCCACGTAG[A/G]TGATGGGGAAGATGC | 10580 |
rs370227532 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484947 | CCACTGCACTCCAGC[C/T]GGGACAACAGTGCGA | 10580 |
rs370241199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427582 | AGGAGTCTGGAGAAT[A/G]AGTGTTAACTGGGCA | 10580 |
rs370242556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456569 | TGTGGTATTCTGTTA[C/T]GCAGCAAGAAACAAG | 10580 |
rs370290679 | snp | C/T | 3.29717e-05 | 0.00406015 | missense | SORBS1 | GRCh38.p7 | 10:95384090 | ATCTCACTTTTTGAG[C/T]GAGGCACAGAAAGGG | 10580 |
rs370292762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554525 | AAAAAATTAGCTGGG[A/G]GGGTGGTGGTCTCCT | 10580 |
rs370292890 | snp | A/G | 1.68846e-05 | 0.00290552 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336574 | GCTCGCCACCTCTAT[A/G]CCGCTCTGTCTGCTC | 10580 |
rs370316382 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361629 | TTTTTTTTTTTTTTT[-/G]TAGTTTTAGTAGAGA | 10580 |
rs370332797 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364475 | TTGTTTTTCTTGAGA[C/G]AGAGTCTCGCTCTGT | 10580 |
rs370366390 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501060 | CACAACGTCCAGTTC[A/T]GCACAGTGGCAGCAA | 10580 |
rs370367662 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434999 | AGCTCTGGACAAAGA[C/T]TTACAGAGGCACACA | 10580 |
rs370369419 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511726 | AGTTTTCTAGAGGAG[A/G]GACGGCTAGTAGGAA | 10580 |
rs370371759 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405058 | ATATTTGCAGTCACT[-/C]CCCACCATTGTCAAC | 10580 |
rs370375496 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347014 | CCCTCTGTTCCCAGA[C/T]GCCCAGGTCCAAGTC | 10580 |
rs370414686 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415101 | GAATCCTTTTAACAC[G/T]TTATGAGAGAGAAAG | 10580 |
rs370419125 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432347 | CACCCCCCCCCCCCA[-/A]GAGGTATCTGATGAA | 10580 |
rs370475426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453312 | AACAAAAGCAAAAAA[C/T]CTACTTACATTAATT | 10580 |
rs370478348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502597 | GAACAGACCAGTGTC[A/G]CCTGAACATTACTGG | 10580 |
rs370483259 | snp | A/G | 1.64955e-05 | 0.00287184 | missense | SORBS1 | GRCh38.p7 | 10:95432486 | GTTTCCTGAGGGCTC[A/G]CAGGGCTACTGCTTG | 10580 |
rs370485016 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545658 | ACTGTACTCCAGCCT[A/G]GGTGGCAGAGTGAAA | 10580 |
rs370514230 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552142 | GCAGTGGCTCACACC[C/T]GTAATCCCAGCATTT | 10580 |
rs370528182 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391875 | AGCCCTTAGGCTAGG[C/T]TTTGATAGGTTTATT | 10580 |
rs370528445 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367214 | TACCCAGCTTTTCCT[-/T]TTTTTTTTTTTGGGT | 10580 |
rs370529043 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377844 | TGGGAATGGTTAGGC[-/TT]TTTTTTTTTTTTTCT | 10580 |
rs370552641 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451036 | ACCTGAAAGAAAAAA[-/A]TTCTAGGAGACAAGC | 10580 |
rs370553523 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494503 | GCTAAGACTGGCAAA[C/G]TAAATGCCGTGTACC | 10580 |
rs370554120 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349810 | TCCCTCTTTTCACTA[C/T]CTCTTCTTCCCAGAC | 10580 |
rs370556240 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562589 | AACTGATTTTTGTCA[A/G]CTGCCCTTGCAAGCA | 10580 |
rs370559761 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482246 | TTTTCTCTGCTAAAG[C/G]CTCTGTGCCATTTAA | 10580 |
rs370584717 | snp | G/T | 1.65116e-05 | 0.00287324 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394993 | TATGCTGTCTAAGTT[G/T]ATGGTACCTTCGGAA | 10580 |
rs370589891 | snp | C/G/T | 5.47643e-05 | 0.00523256 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336537 | TGGCTCCCACCTCTC[C/G/T]GAGCAGCTTTCCTCC | 10580 |
rs370626121 | snp | A/G | 0.000166204 | 0.00911452 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341459 | GAAGAGAAGAAAGCA[A/G]GGAAACAAGAGGAAA | 10580 |
rs370631904 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558549 | TGAATAAACCAGCAA[C/G]TTAAACATCCACAGG | 10580 |
rs370653627 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549407 | ACGCTGGTCTATAAC[C/T]GGTGCTCAATAACTA | 10580 |
rs370654534 | snp | C/T | 3.30028e-05 | 0.00406205 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357719 | GACACTTTTATAAAT[C/T]TGTCTCTCATTCTCC | 10580 |
rs370654920 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497756 | CCACCACCCCACCCC[-/C]AGGCTAGAACTGATA | 10580 |
rs370674573 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426508 | AAGTTGGACTGGAGA[C/T]TGAGAACTGCCCTGT | 10580 |
rs370708132 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95381769 | ATATTTTCTTGTGTC[C/T]ACTTTCTTATCTGGG | 10580 |
rs370718590 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366346 | GCAACAGAAGTAAGG[A/G]CCACAGAGGTACTAA | 10580 |
rs370724377 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377576 | GTCTGTCCTCCTGCA[C/T]CCAGATAAGACTTCC | 10580 |
rs370758021 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538855 | GTCTCACAAAAAAAT[A/T]AAAATAAATTTTACA | 10580 |
rs370770813 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430170 | AGTGCCTCAAATCCA[C/T]ACACGGGGCCGGGCA | 10580 |
rs370784110 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510796 | AGTGAGACTCTGTCA[A/T]AAATTTTTAAAGTGG | 10580 |
rs370790980 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557759 | CCCTCACTTCACCCC[A/G]AGGGCTGCAGAAGAG | 10580 |
rs370803263 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455807 | GGCATGGTGCCGTAT[A/G]CGTGTAATCCCAGCT | 10580 |
rs370813463 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521312 | CAGGCAGAGGTGAAC[A/G]GCACACAGAGAGCTT | 10580 |
rs370828487 | snp | A/C | 0.000134033 | 0.00818525 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318285 | GTTATTCCCTCAATA[A/C]ACAACTAGTAAGAAA | 10580 |
rs370830568 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464332 | TTAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAGGC | 10580 |
rs370839434 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336611 | ACTTCCTGGAAAAGC[A/G]CTACCCAGGGGCTTG | 10580 |
rs370850385 | snp | A/C/G | 0.00114841 | 0.0239384 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414501 | AAGCTTACGGTACTC[A/C/G]AAACAGCTCCCGTGA | 10580 |
rs370866519 | snp | C/T | 8.30668e-05 | 0.00644411 | missense | SORBS1 | GRCh38.p7 | 10:95354904 | TCATCATGACGTCTT[C/T]GAATAAATTCTTCCG | 10580 |
rs370874351 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95546253 | CCAAACAAGAATGGA[C/T]TGGCAAAGCCAGTTA | 10580 |
rs370878698 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469299 | CCTGGTTTACCCAAA[G/T]TATAGATTCTGGCAC | 10580 |
rs370885917 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334758 | GGGTTGACTTAGAAT[A/G]TTTATAGAATTGTTC | 10580 |
rs370888361 | snp | A/G | 1.74827e-05 | 0.00295652 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336988 | AGTAGGTTTTGTGTG[A/G]GGAAGGTAGGGCCAG | 10580 |
rs370900311 | snp | C/T | 0.000153988 | 0.00877328 | missense | SORBS1 | GRCh38.p7 | 10:95437529 | GTGCCAAGCCATTCA[C/T]CACAGCTTTGGAACC | 10580 |
rs370914236 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340027 | ATTCTGTCGCACACA[A/C]ATATAATGATTTAAT | 10580 |
rs370915032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466079 | CTTAAACACGAGAGG[C/T]GGAGGTTGCAGTGAG | 10580 |
rs370924738 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529744 | AAGTAGTGCAGTGAC[A/T]TGCCCAAGTCCAACT | 10580 |
rs370932474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354047 | GTGATTTTTCCAGCT[C/T]TTAATTCATTTCAGG | 10580 |
rs370947166 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540198 | AACGGCCTCCCATCA[C/T]TGGCCTCTAAGGTCT | 10580 |
rs370948576 | snp | A/C/T | 0.000339882 | 0.0130324 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421937 | ACTCACCAGTCCCCA[A/C/T]CCTGCCCTTGGGCAC | 10580 |
rs370958884 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562874 | CCACGGCCTTCCCCT[A/G]TCTGCACCTCATCCT | 10580 |
rs370981831 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330013 | GTCACTTTCCTCAGG[A/C]CTTGGTTTCCTCATC | 10580 |
rs370991579 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466747 | ATCTTTAATTACCCA[G/T]ATTCAAGAGAAGGAA | 10580 |
rs370994417 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414695 | ATCTAGAGTCGGGAA[A/G]GTCAGAGGTGAGGCG | 10580 |
rs371005855 | in-del | -/TGTGTGTGTGTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365174 | CATTTACTAACCTTA[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 10580 |
rs371007922 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436752 | ATAAATTCCCTCATC[C/T]TATAGATAAGGGAAC | 10580 |
rs371025891 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380632 | TGGTGCATAGTGAAC[G/T]CTGAAGAATGACAAC | 10580 |
rs371033125 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340345 | AAGCCTCTTACAACC[A/G]CCTAGGAGAGAGCCA | 10580 |
rs371038721 | snp | A/G/T | 1.64841e-05 | 0.00287085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437587 | GAGCATGAGGTTTGT[A/G/T]AGTAAGCTGCCCCAG | 10580 |
rs371064991 | snp | A/C | 1.79745e-05 | 0.00299782 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337091 | ACTGGCCCTTGGTGA[A/C]AAGGCGAGGTGGTCA | 10580 |
rs371080838 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472938 | TCAGGAGGCTGAGGC[A/G]GAGAATTGCTTGAAC | 10580 |
rs371090486 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343987 | ATTACGAATTCCCCC[C/T]CCCTTCATCCCCAAC | 10580 |
rs371095732 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441230 | TGAATGGCAGGTTCG[C/T]GATAAATCCCAATGG | 10580 |
rs371097608 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549006 | CAAAGATAAGAGACC[A/T]GTTCCTAGCTCAGTC | 10580 |
rs371104773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533967 | GCTGAGCCACCAGGC[C/T]GTCTAGAAATCATTG | 10580 |
rs371107351 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369185 | ATTCGCTTTTCCCTC[C/T]GCCTCTGTGAACTCT | 10580 |
rs371113563 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490073 | ACCTAAGACCTCCAA[-/C]CATCCACTAGCTGTC | 10580 |
rs371121148 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552284 | GCATGCGCCTGTAAT[C/G]CCAGATACTTGGGAG | 10580 |
rs371169097 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342890 | ATTATTATTTTTTTT[A/T]TTTTTTTTGAGACGA | 10580 |
rs371179437 | in-del | -/ACACACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432313 | AGGGGACCGTAAGAG[-/ACACACAC]ACACACACACACACC | 10580 |
rs371180804 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330517 | TTTTTGTTTACTTTT[A/T]AAAATTTTTTTGAAA | 10580 |
rs371182069 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378773 | TGTGTGTATGTATGT[A/G]TGTATATATTTAACT | 10580 |
rs371187899 | snp | C/G | 0.00147137 | 0.0270836 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399222 | TTGTTAGCTGAAGCT[C/G]TTTTGGTAGCTGCAA | 10580 |
rs371207086 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362874 | CAACAGAACGGACAA[A/G]AAGTTCCAGCCTCAT | 10580 |
rs371218190 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458550 | CCTTGAACTCCTGGC[C/T]TCAAGTGATCCTCCT | 10580 |
rs371229947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437925 | CCAAGGAAGGAAGGC[C/T]GGCAGGCCCTGTCGC | 10580 |
rs371245459 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523347 | AAAAGACAACGGTGC[A/G]TGGAACACGGCTCTA | 10580 |
rs371274943 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501832 | TGACTGGTACTCTTG[A/C]CTGAACATTCTGAGT | 10580 |
rs371275455 | in-del | -/T | 0.429388 | 0.174127 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404500 | GTTTACACGTGTGGC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs371294362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450431 | CTAACATAGACCATA[C/T]AACATGGGAAAAGAC | 10580 |
rs371297114 | in-del | -/AATATTTT | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476595 | TTCAATGGATGGAAC[-/AATATTTT]ATTATTTTCAAAGTA | 10580 |
rs371320683 | snp | A/G | 3.38095e-05 | 0.0041114 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414629 | GGAGCCAGAGGCGCG[A/G]GCTGGCTGGCTGTGG | 10580 |
rs371341162 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549580 | GTCTGGTAGGGAGTT[A/G]CTCTTACAATAAAAA | 10580 |
rs371382690 | snp | C/T | 8.23988e-05 | 0.00641815 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384041 | GGGTAGTGTGGCCGA[C/T]CTCTTGACTACCTTC | 10580 |
rs371397357 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372344 | GAAAAGACGGGGGGG[-/A]AAAAAGAAAAAAAAA | 10580 |
rs371468457 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415815 | CAAATGTTATTGGAT[A/G]AACAAGGTACATATA | 10580 |
rs371480114 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497126 | CAACTTGTTTACTGC[A/G]GTACCCCCAGCAACA | 10580 |
rs371480389 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | SORBS1 | GRCh38.p7 | 10:95397252 | ATCTGTTTAAACATA[G/T]TCTTGTACCAGTCTT | 10580 |
rs371482294 | in-del | -/CTCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506069 | CCAATCTCTCTCTCT[-/CTCT]GTCTCTTTTTCTTGG | 10580 |
rs371499155 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442526 | TGGCACCCCCCCCCC[-/G]CACCCTTACTTATGC | 10580 |
rs371501809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443729 | GTTGCTTTGCCTTAC[C/T]GTCCTTGTAATTAAG | 10580 |
rs371516597 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405445 | AGCAAGATGCTGTAT[A/C]AAAAAAAAAAAGAAA | 10580 |
rs371535809 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392465 | CTCCAGGGAGGATGT[C/G]TTTTTAGAAACTTGT | 10580 |
rs371536279 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536859 | CACTAGTAATAGTCA[C/T]ATTGGGACGAAGCAC | 10580 |
rs371542461 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392797 | CTGTCTTTGGACCAA[-/C]CAGCCAAGCTGACTG | 10580 |
rs371566996 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359912 | CTGCCGAGGGTGGGG[A/G]TCAGAGCTCCCCCAG | 10580 |
rs371583409 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517174 | ACAGTTGATATTCAA[C/T]AAGTGGCTGCATTGT | 10580 |
rs371589846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315274 | AAGTACTTTCCCCTA[C/T]CTTATCTCACTTAGG | 10580 |
rs371600137 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499077 | TGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10580 |
rs371609048 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554995 | CAAGTGACTCTCCTG[C/T]CTAAGCCTCCTGAGT | 10580 |
rs371609724 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518032 | AGGGATGCCAGCCTC[A/T]CCACAGCTGGCAGCC | 10580 |
rs371623410 | in-del | -/GTTGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332397 | TTACTCCCCCGGTGA[-/GTTGG]AGATCCTAAACTCCT | 10580 |
rs371632546 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538204 | GTGAGTCCCAGGTGA[C/T]AGAAAGGAAGTGGCC | 10580 |
rs371633552 | snp | C/T | 5.00605e-05 | 0.00500277 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432598 | AGAAAAGGTCCAAAA[C/T]TGAAGACTGAATCCA | 10580 |
rs371642515 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459656 | GGGACAAGCAGCAGA[C/G]TCCTTTCAACGGGGG | 10580 |
rs371642908 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343003 | TCCTGCCTCAGCTTC[A/C]CAAGTAGCTGGGAGT | 10580 |
rs371647506 | in-del | -/T/TT | 0.0898077 | 0.191933 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338713 | TCTGCTTTCCTGCAG[-/T/TT]TTTTTTTTTTTTTGA | 10580 |
rs371654288 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484977 | AGACCCTGTCTCAAA[C/T]AGAAAGGAAACAAAA | 10580 |
rs371656356 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384721 | TGAAAGGCCTCTTAC[C/T]GGGGCCTCGGGCTGC | 10580 |
rs371661560 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336757 | GGCCTCTTTCGCCTG[C/T]CCCCCTCTCTGCTTT | 10580 |
rs371683133 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360188 | CCTTCAGTTTAATGC[-/TA]TGTTTCCTCTTTTTT | 10580 |
rs371685978 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330360 | ATTTGATCATGCAAA[C/T]GATGGGATTTTTCAA | 10580 |
rs371691882 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335998 | GCATTCTCCTCTCCA[C/G]AACCAAAACACCTTT | 10580 |
rs371693525 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557529 | TCAGCATCAGCCAGC[A/T]TCACCACCCGCACAC | 10580 |
rs371694168 | in-del | A/CAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502998 | ACACATACACACACA[A/CAC]ACACACACACACACA | 10580 |
rs371698537 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366995 | CTTTACACCAGATGT[A/G]GCCTGTCTCAGTCAC | 10580 |
rs371704654 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440360 | AACACTCACGAAATA[C/T]GGCAGGATTGGGAGA | 10580 |
rs371734949 | snp | C/T | 8.94526e-05 | 0.00668718 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337113 | AGGTGGTCAGTGTTA[C/T]AGATAGAAGCCTCTG | 10580 |
rs371741100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472961 | GCTTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 10580 |
rs371747887 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553145 | TTGAGCCCAGGAGGT[C/T]AAGGCTGCAATGAGC | 10580 |
rs371769812 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386641 | CTCTGTCTTGAAAAG[-/A]AAAAAAAAAAAGTAA | 10580 |
rs371776709 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528820 | GCTATTCAGGAGGCT[A/G]AGGCAGGAGAATCGC | 10580 |
rs371784791 | snp | A/C/G | 0.000625787 | 0.0176777 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414628 | AGGAGCCAGAGGCGC[A/C/G]GGCTGGCTGGCTGTG | 10580 |
rs371790561 | snp | A/G | 8.85779e-05 | 0.0066544 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339118 | ATGAAAACCAGTGAC[A/G]AGAAGCTTAGATACC | 10580 |
rs371812016 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459303 | CCCCTCTGCTAATAT[C/T]GCAGCTCTAACAACT | 10580 |
rs371818147 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508671 | TGGCTCCTAGAGAGT[A/G]AGTTCCTCATTGCCA | 10580 |
rs371831256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525025 | TCAAACCTTCAGATG[A/G]CACAAAACTGGGAAG | 10580 |
rs371840093 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382667 | TCTCTATTCTGTTCC[A/G]TTGGTCTATATGTCT | 10580 |
rs371843618 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365151 | TAGCATTTGCCACTT[G/T]GCCTTTTCATTTACT | 10580 |
rs371852100 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376483 | TTAGCCATCTATGCC[A/G]GTTGAGTAGAGCTGA | 10580 |
rs371854813 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342447 | TCCATTACTTTTTTT[-/T]CATGAGACGGTCTCA | 10580 |
rs371887870 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462342 | GAAGCTTTTTTTGAA[A/T]AGGTTTTATTTTTGA | 10580 |
rs371896127 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360456 | TCTAAGAGTATGCTC[C/T]TATAACAAGTAGCTG | 10580 |
rs371971675 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479826 | GACGCACTTTGGAGA[A/T]GGGAGGTGTACAAAC | 10580 |
rs372001868 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457037 | ATCAGAAAATAAAAG[G/T]TGTCGAAAAATCCTT | 10580 |
rs372012459 | in-del | -/T/TT/TTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534102 | CATGCAGCTTTTTCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10580 |
rs372014652 | snp | A/G | 1.65214e-05 | 0.0028741 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322846 | GGAGACATTTTAGCA[A/G]ATGTCACATTGGAAA | 10580 |
rs372030074 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408615 | AGGCATTTTTTAGGA[A/T]GACAAAACTAGAATT | 10580 |
rs372033803 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468778 | GGAAATAAGGAGGCT[C/T]AGCCTAAAGAAATGT | 10580 |
rs372044001 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504227 | CAAAACCAAGAGAGA[A/C]GCCCAGATTGTCTGT | 10580 |
rs372083433 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397110 | ACCAGTACCTAATGA[A/G]GTCCAACTGCAGGAC | 10580 |
rs372087493 | snp | C/T | 0.000121043 | 0.00777863 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355563 | GGGCACAGAGGAGGA[C/T]GGGATAATGCAAGCA | 10580 |
rs372088663 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367754 | AATGTAGATGATTTA[C/T]TTTGACTCATATGTT | 10580 |
rs372103080 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497668 | TGCTCAGGTCTCTAC[C/T]GCTTAAAACATCTTT | 10580 |
rs372104524 | snp | C/T | 1.65647e-05 | 0.00287786 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384304 | TTGAACAAAACAAAA[C/T]GTAGTCAGGAGAAGT | 10580 |
rs372104944 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476200 | AGCTGATGCCAATAA[C/T]GACAATGATGACAGA | 10580 |
rs372139303 | snp | A/G | 3.29799e-05 | 0.00406065 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441095 | TGCCCAGTTTGGTAG[A/G]TAAGAGAAAGATGAG | 10580 |
rs372150905 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522286 | TCAACCCATACTTAT[C/T]TCTTGAGTCCCTACT | 10580 |
rs372159851 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467672 | TTGAGAGGTGTTTTT[A/G]TTTTTTGGAATAGAA | 10580 |
rs372181356 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541242 | CTGGCCTGAGGTCTC[G/T]CCACTAGATCACAAC | 10580 |
rs372190093 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407004 | TGACCTTTACCTTCC[A/C]CAGCCGCTAAATATA | 10580 |
rs372192041 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476018 | ACTCTGCATCTACTG[C/T]GCTCCAGGCTCCGTG | 10580 |
rs372192460 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516059 | CCTGAATTGACATCC[A/G]CACCCACCCCCCACC | 10580 |
rs372212462 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499229 | AGGCGTCCACCACCA[C/T]GCCCAGCCAATTTTT | 10580 |
rs372244331 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458716 | CTTTGGTGCTTCTGA[A/G]CTCATTCATTCAGTA | 10580 |
rs372284980 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-5-prime | SORBS1 | GRCh38.p7 | 10:95441155 | GTGGCAGGACAAGTC[A/G]TCTGCAACTGGGGCT | 10580 |
rs372298300 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421146 | CACTCTGGCCTGGGC[A/T]ACAGATAGAGACCCT | 10580 |
rs372314775 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354383 | GAGAGTTATAGGCAA[C/T]TTCCTCAAATTGTTT | 10580 |
rs372316148 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315671 | TGCTAAGCCAGGAGC[A/C]TTGAGCCATCTGGGA | 10580 |
rs372319830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369813 | AATTCCACAGTGGCT[A/G]ATCTGGTTCCTTCAC | 10580 |
rs372333087 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514800 | TACAAAAGTCACTTC[A/G]ACTTCAGATTCATAC | 10580 |
rs372353717 | snp | C/T | 3.55967e-05 | 0.00421866 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336548 | TCTCCGAGCAGCTTT[C/T]CTCCCCGCCTGCTCG | 10580 |
rs372376359 | in-del | -/TTCTTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390631 | TTTCCTAACTATATA[-/TTCTTTT]TTTTTTTTTTTTTTT | 10580 |
rs372388702 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382257 | GATCTTAGACAAGTA[A/T]TTCACCTCTTGGTAT | 10580 |
rs372437093 | snp | C/T | 5.01702e-05 | 0.00500825 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341513 | TTGGTAAATAAATGG[C/T]GCTTTGGGCACTGTC | 10580 |
rs372438843 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493695 | GAGGAAACAAACAGG[A/C]AGAATTCACCTGAAG | 10580 |
rs372439393 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394742 | AGTGACAAATCCCAA[C/T]TGACTCTTTCGAATG | 10580 |
rs372467240 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383371 | CAGTGAGCCGAGATC[A/G]CACCACTGTACTCCA | 10580 |
rs372468539 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398795 | CAGCTTTTCCTCACA[C/T]TTACTTGACCACGAA | 10580 |
rs372493677 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496308 | CCCTTTTCTGACTTT[A/G]AAAAAGACTTCTCTC | 10580 |
rs372503294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551647 | AATGGAAAAAGGGAC[C/T]TGGAAGAAACAACAT | 10580 |
rs372505638 | in-del | -/GA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527128 | TCAGCTCATATGAAA[-/GA]ATTTTAACAATTAGC | 10580 |
rs372512499 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313091 | AGCTCACCCCCTCCA[A/G]TTCCATAACCTTTTC | 10580 |
rs372517142 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526987 | TCTATCTTGTTTACT[C/T]GTATTCCTCCTGAAC | 10580 |
rs372527646 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332738 | GATTACAGGTGTAAG[C/T]CACCATGTCTGGCTT | 10580 |
rs372543454 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458901 | ATACAAGAATCCCCA[C/T]CTCACCTCCCCTGCA | 10580 |
rs372556201 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352523 | ACTCATCAAATGGCT[A/G]TGGGATTTCCAGTAC | 10580 |
rs372561153 | in-del | -/CACACA/CGCGCGCACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358716 | ACATGCGCGCGCGCG[-/CACACA/CGCGCGCACA]CGCGCGCACACACAC | 10580 |
rs372637601 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455062 | CTAGACTTAGTATAA[C/G]TTGGATTTGAGTTGC | 10580 |
rs372659848 | snp | A/G | 1.6501e-05 | 0.00287232 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414700 | GAGTCGGGAAGGTCA[A/G]AGGTGAGGCGGCAGA | 10580 |
rs372685548 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366282 | GCCCTTGAGGAGTTT[A/C]TAATACACTAGCAAT | 10580 |
rs372691616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496928 | AGCTCTTTCCCTTTT[C/T]CTCACCACGGAAAGA | 10580 |
rs372693402 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487615 | GAGGCAAAAATGTCT[A/G]TGGCAGCTGGAGACT | 10580 |
rs372698313 | snp | C/T | 0.000247887 | 0.0111302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394980 | CTCGGACAACAGATA[C/T]GCTGTCTAAGTTTAT | 10580 |
rs372706083 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433778 | AGCACCTCTTGTATT[A/G]AACGCAATGCACGAA | 10580 |
rs372733924 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371339 | ACCTGTGGCACGTTT[A/G]CACTGGGTGCTTTAT | 10580 |
rs372744112 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457777 | ATTTGTGCAGAACTT[C/T]ACAGGCGACAGGACA | 10580 |
rs372746792 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513023 | GGCAAATGTTCCTTT[A/T]GGACTTGCTTCAAAC | 10580 |
rs372747658 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518560 | GGATGCTGTTGAGCA[C/T]ACAAAAACACGTGCC | 10580 |
rs372753105 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539057 | TACCCACCACTAGCC[C/G]CACCTTGGCCCATCA | 10580 |
rs372762012 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333710 | CTGGGGGCAGAGGTT[A/G]CAATGAGATTGTGCC | 10580 |
rs372777541 | snp | A/G | 4.95315e-05 | 0.00497627 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414690 | AAATCATCTAGAGTC[A/G]GGAAGGTCAGAGGTG | 10580 |
rs372799262 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427604 | AACTGGGCAATTTCA[A/C]GGGCTCTCTCTGTCA | 10580 |
rs372805230 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462074 | AATTAGACAGGCTTT[-/G]ATCTCTAATAGTCCA | 10580 |
rs372808628 | snp | A/G | 3.37371e-05 | 0.00410699 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351184 | GCTTTGGGTCAAGCA[A/G]CAGATTGAGGTGACC | 10580 |
rs372810233 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419679 | TCTCCTGCCCTGGGG[C/T]TTCTTTTAGTCCTGA | 10580 |
rs372817230 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525138 | GTGCAAAAGTACGGG[C/G]TGGGGGCAGGTCTAA | 10580 |
rs372827782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530803 | TTATCTCTGCCCACC[C/T]TGTACATGTTACCTG | 10580 |
rs372834257 | snp | A/C | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561559 | CGTGACAGGAAGGGG[A/C]GTGTGCGCGGATGGG | 10580 |
rs372840514 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313633 | GATGGCAATATGACA[A/G]TGCTTTCTAGGATCC | 10580 |
rs372841961 | in-del | -/GAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325429 | CAAATATAGTAAGAA[-/GAA]CCTGATATTTTACAA | 10580 |
rs372880988 | in-del | -/TGTTACCT | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425910 | GCTTCTTTCAATAAA[-/TGTTACCT]TAGAGCTCCCAAGCT | 10580 |
rs372885973 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378982 | GGTTTGGTCGCTCAA[A/G]CCTGTAGTCCCAGCA | 10580 |
rs372901787 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323046 | TTGGAAACATGGCTG[C/T]AGTGAGGTGAGGATG | 10580 |
rs372905770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456295 | GTTGAAATCTAGTTG[C/T]CATTGTGATAATATT | 10580 |
rs372942686 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371847 | TTTTATTACCTAACC[-/A]AAAAAAAAAAAGCAT | 10580 |
rs372962780 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484289 | GATAAGATTTTAAAC[A/G]AACAGTAAGTCAGGG | 10580 |
rs372968425 | snp | A/C/T | 3.29534e-05 | 0.00405904 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336868 | CACTATCAGAGCTCC[A/C/T]CAGCGGCAGCTGCAA | 10580 |
rs372994478 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353129 | CTGCTCACCTTCTTA[C/T]GTAACTTCTAATATA | 10580 |
rs373010729 | in-del | -/ACACACACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432325 | GAGACACACACACAC[-/ACACACACA]CCCCCCCCCCCCAAG | 10580 |
rs373020225 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447164 | AAACAAACAAACAAA[A/C]AAAAACAAAAAAACC | 10580 |
rs373031350 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495275 | CTCTGTCCCAACCCC[A/C]CAAAAGACTTCACAA | 10580 |
rs373032618 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339002 | CATGAGCCACCACAC[C/G]CGGCCTCCTGCAGAC | 10580 |
rs373035603 | snp | C/T | 1.66023e-05 | 0.00288113 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375961 | TATAACCACTGAAGC[C/T]ATTAAACTTACCGGT | 10580 |
rs373035817 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347441 | CTCTATCTGGAATTT[C/T]TTTTTTTTTTTGAGA | 10580 |
rs373065139 | snp | A/C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529050 | AGTTTGGAACCAAAG[A/C/T]GGAGATTCCATTTGT | 10580 |
rs373067584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373119 | AAAACTGATTCCCAG[C/G]CTCTTTGTAATAAAT | 10580 |
rs373067597 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350230 | ATAGAAACAAATATT[A/T]ATCTACTGTACTGAA | 10580 |
rs373078046 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316323 | CTAGGCGTGGTGATG[A/C]GGGCCTGTAGTCCCA | 10580 |
rs373086382 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489421 | TCACAATACTTAGTG[A/G]ACACCCATCAGGTGT | 10580 |
rs373094193 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455602 | ATTTACATGTAAAAC[A/T]TTTTTTTTAACTTTA | 10580 |
rs373108964 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510787 | GACAACACAGTGAGA[-/C]CTCTGTCAAAAATTT | 10580 |
rs373112830 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551586 | ACAGTCAAGGATCAG[C/T]ATGCATGGAAGGATA | 10580 |
rs373120168 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541311 | CAAGTCCCCACTCAC[A/G]CCCTCTTTCCCCAAC | 10580 |
rs373128547 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493091 | AGTTCAGGAGTTTGA[A/G]ACCCGCCTGACCAAC | 10580 |
rs373166548 | snp | C/T | 0.000121381 | 0.00778948 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356422 | ACTTGCTCAGCCTTC[C/T]GGACAGGTCCAGGGA | 10580 |
rs373168612 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314505 | TTTCCCCATCCACAC[C/T]TCAGCAGGTTGAGTG | 10580 |
rs373176370 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405726 | ACTTGCCCATATCTC[C/G]CAACCCCTGACTCCT | 10580 |
rs373191503 | snp | C/T | 0.00029755 | 0.0121937 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434606 | TTAGAGAAAATCGAC[C/T]GACCCAAGGAGATAC | 10580 |
rs373195935 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533240 | TGGGGGTAGGTTCGC[A/T]TAGGCCTGCCCACTG | 10580 |
rs373199736 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344892 | CTCCGGCATTAGCAA[C/T]GTTGATAAAAGGTGA | 10580 |
rs373201803 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416493 | ATCCTTGGCTGACTG[C/T]ATCTTTATTAGACAT | 10580 |
rs373216810 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482205 | TTACACCATCCTGTG[C/T]TGAGCATGTTCTACA | 10580 |
rs373251721 | snp | A/C/T | 0.00358891 | 0.0422285 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545555 | GGGAGTGTTGGCAGG[A/C/T]GCCTGTAGTCCCAGC | 10580 |
rs373267375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429306 | GCTGGGATTACAGGC[A/G]TGCAACACCATGCTT | 10580 |
rs373275810 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409719 | GGAAGACGTGAGCTC[C/T]GAACAAAATAATTAA | 10580 |
rs373282696 | snp | A/G | 0.000153988 | 0.00877328 | missense | SORBS1 | GRCh38.p7 | 10:95318401 | CATCATCATTCTGTG[A/G]TATATAGCTATATAA | 10580 |
rs373300533 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431896 | GGGCCTTTGAGCTAC[C/T]TTCCTGATCCTGCTC | 10580 |
rs373353960 | snp | C/T | 0.000139843 | 0.00836074 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381651 | TAAAGAACATGGGCA[C/T]GGTGAGACAAAATAA | 10580 |
rs373366585 | snp | C/T | 5.27394e-05 | 0.00513487 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336554 | AGCAGCTTTCCTCCC[C/T]GCCTGCTCGCCACCT | 10580 |
rs373377513 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95341129 | TACAGGCATGAGCCA[A/C]CGTGCCCAGCCCTTA | 10580 |
rs373377893 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363343 | CATGCATACAGATTT[C/G]TGACACATTTGTAAA | 10580 |
rs373428340 | snp | A/G | 1.81496e-05 | 0.00301239 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414571 | GAGGGACCAGCGGAG[A/G]TGGTGGTGAGAAGGA | 10580 |
rs373432735 | in-del | -/GGGATTACAGGCCTTAATGCAATTCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340830 | GTTTCCCAAAGTGCT[-/GGGATTACAGGCCTTAATGCAATTCT]TTTTTTTTTTTTTGG | 10580 |
rs373435464 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377858 | CTTTTTTTTTTTTTT[-/T]CTTAAATAAAATGTA | 10580 |
rs373437179 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383185 | TTCAGAGGGCATTTT[G/T]AGAGATAAGAACTCA | 10580 |
rs373447783 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320672 | TGTGAGCCACCGCAC[C/T]TGGCCTCACTTACAT | 10580 |
rs373465807 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418266 | TATTTTTAGTAGAGA[A/C]GAGTTTTCACCATGT | 10580 |
rs373476844 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366679 | CGGCACCTCCCTCCC[A/C]CCGTCTATTTTTTTT | 10580 |
rs373480293 | snp | A/T | 3.30311e-05 | 0.0040638 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321932 | CAGTCCTCTGAGAAC[A/T]TGAGAATCGAAGTTC | 10580 |
rs373481146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491372 | ATCATCTTTAATGGA[A/G]ATCACAAACTGAAAG | 10580 |
rs373485671 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521068 | CAAAGAATGGTTCCA[A/G]TTCTATCCATGCCCT | 10580 |
rs373494742 | snp | C/T | 0.000131798 | 0.00811675 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336809 | TTCGCGCCATGGCTG[C/T]CTCTTGCTCTGGCTG | 10580 |
rs373494935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466419 | GTACTCCAGCCTGGC[A/G]ACAGAGCAAGACTCC | 10580 |
rs373499279 | snp | A/C/G | 8.3124e-05 | 0.00644639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394719 | ACTATCCACCAGGAA[A/C/G]TAGAGGAAGTGACAA | 10580 |
rs373501845 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390448 | TTTGGGCGTGTTCAG[A/G]GTAGGGGGCGCTAAT | 10580 |
rs373515471 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551102 | TTGCAGTCTGCTCAG[C/G]CTGGTGATTTCCCTG | 10580 |
rs373538432 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415119 | ATGAGAGAGAAAGAA[C/G]AGAACAGGCAGGCAG | 10580 |
rs373539083 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334690 | CACAGGATCCTGGAA[C/T]TGGGCCGGGATGATG | 10580 |
rs373545029 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390549 | TCATCTCTTTTTGGG[G/T]GCTGGGAAGAGTGGT | 10580 |
rs373562778 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426975 | CTAATTTAATGGAGG[G/T]ACGGGGTACCTTCAA | 10580 |
rs373571757 | in-del | -/TGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494078 | CTTCTTTTAAATAAA[-/TGT]AAAAAAAAAAAAAAA | 10580 |
rs373573672 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435280 | CCCCATCTGTTAAAC[A/G]GCAGATGGCCTTGCT | 10580 |
rs373578040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556495 | TCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGATTA | 10580 |
rs373622154 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432085 | GCTCTGAGAAGCCCA[A/C]CCTCTAGCCCATCGC | 10580 |
rs373629844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536772 | AAACCTTCAGGGGTG[C/T]CATATGGCCTTGAGG | 10580 |
rs373653047 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323783 | GCTTGAGCCGGGGAG[C/T]TGGAGACCAGCCTGG | 10580 |
rs373666462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419388 | CACGTGGGCTAGCAC[A/G]CACCAAAGGGACTGG | 10580 |
rs373673522 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393396 | CAGTAAGAGTTTGGT[C/G]AATGATTGAATGAAC | 10580 |
rs373711349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522612 | GGGGACACACAAGAG[C/T]CGATTTCCAAGGCTG | 10580 |
rs373711423 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503560 | GGGCCTAGCACCATG[A/T]AGAACTTCTAAAATA | 10580 |
rs373712696 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350618 | CTGCAAAAGTCTTTG[A/G]GCTTCAAAATTCTTT | 10580 |
rs373723294 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386790 | GGATGCAGGTAACAG[A/G]GGCGTCTGAAGAACT | 10580 |
rs373738328 | snp | C/T | 2.66898e-05 | 0.00365297 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422229 | GACCTACACGTGGTG[C/T]AGAAAGGATGAAAAC | 10580 |
rs373738926 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415001 | TCAGAGTACATGAGA[C/T]AGTCGGAGCTGGCCA | 10580 |
rs373742181 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95341366 | TTCCAAAACCTGCAC[C/T]GGTGTCAACTTTTTG | 10580 |
rs373781624 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342839 | TTCCATATCCATTCC[C/T]TTGCTTGCCTCAATA | 10580 |
rs373828058 | snp | A/T | 1.64993e-05 | 0.00287218 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397294 | GTGTTCTGTAGAAAA[A/T]CAAAGGCAAAGAGCA | 10580 |
rs373835289 | in-del | -/A/C/GG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560091 | GGGCTGGGCGGGGGG[-/A/C/GG]GGGTGTTGAGGGGAG | 10580 |
rs373846895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478256 | GTGACTGAGGCAGAA[A/G]ACAGGTGTGGAGCTA | 10580 |
rs373849099 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548429 | ACTACTTATGTGTCA[C/T]GCATAGTTCTTTTCT | 10580 |
rs373852694 | snp | C/G/T | 1.64985e-05 | 0.0028721 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322051 | AAGATGATTTATTGT[C/G/T]AGAAGGGGATACCTT | 10580 |
rs373853702 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475934 | CCAGGATTTGAAACT[A/T]AAGTCTATGTGACTG | 10580 |
rs373856545 | snp | C/T | 3.30814e-05 | 0.00406689 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351380 | CGCTAAAAGTTTCTG[C/T]CATAAAATTGCATAA | 10580 |
rs373858123 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333755 | TGGGTGACAGAGTGA[G/T]ACCCTGTCTCAAAAA | 10580 |
rs373867184 | snp | A/G | 3.32889e-05 | 0.00407963 | missense | SORBS1 | GRCh38.p7 | 10:95354928 | TCTTCCGTGGATTCC[A/G]AGTAATCAGCTGGTA | 10580 |
rs373873828 | snp | A/G | 4.94189e-05 | 0.00497062 | missense | SORBS1 | GRCh38.p7 | 10:95399082 | TGCTCTTCACCACCC[A/G]CCTACTGTCATCCTT | 10580 |
rs373881653 | in-del | -/CC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540045 | TAGGGGGCCTTTAAA[-/CC]CAGCCACAAGCGCCA | 10580 |
rs373894291 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380282 | ATGACTAAGAACCAG[A/G]GAAAGGAGCTGGAAA | 10580 |
rs373925254 | in-del | -/GGGATTACAGGCCTTAATGCAATTC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340830 | GTTTCCCAAAGTGCT[-/GGGATTACAGGCCTTAATGCAATTC]TTTTTTTTTTTTTTG | 10580 |
rs373926068 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558449 | AATTCCTCAGTTTGG[C/T]GGGGAAGGGGGAGGA | 10580 |
rs373933756 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421744 | AAGGCCTATTTCCAA[C/T]ACCCTGGTACAGACC | 10580 |
rs373938137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363282 | CCTTGCATGGTTGTT[C/T]AATAAATATTAATGG | 10580 |
rs373938187 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348244 | GGGGTTAATGATAAA[G/T]GACAAGTTCACAAGA | 10580 |
rs373938473 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478840 | CCCCTAAAGGTCACA[A/G]CCAAGCAGTGTGATG | 10580 |
rs373943646 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464333 | TAAAAAAAAAAAAAG[A/G]AAAAAAAAAAAGGCT | 10580 |
rs373946262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346352 | CTACAAACAAACTGC[C/T]GTGTTTCAAAAAGGC | 10580 |
rs373953339 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369420 | CCAAGAACTCTAGTT[A/T]TAGAGTTCCAACTGC | 10580 |
rs373971545 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464717 | CCAACAAACATGTTT[C/T]CTTGGTTTACTTATC | 10580 |
rs373977859 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344577 | CCCGGCTAATTTTTG[C/T]ATTTTTTGGTAGAGA | 10580 |
rs373978559 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553578 | AGCTGGGCATGGTGA[C/T]TCACACCTGTAATCC | 10580 |
rs373988991 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520301 | CCTGGGCAACAAGAA[C/T]GAAACTCCATCTCAA | 10580 |
rs373990690 | snp | C/T | 3.295e-05 | 0.00405881 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351315 | ACGCCTGTGTGGCGT[C/T]GAGCTGCAATATCAG | 10580 |
rs373994258 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543271 | GCATAAAAACCCTTT[C/T]GACTATAATCCTAGC | 10580 |
rs374012829 | snp | C/T | 0.000164851 | 0.00907734 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414722 | GGCGGCAGAGGCAGT[C/T]GCTGGGATTGTGGGG | 10580 |
rs374037525 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425804 | GAAGGTTGGTAGCAG[C/T]CCAGGGCCATTTGTG | 10580 |
rs374072625 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434083 | TGAACTGTACTCCCC[C/G]ACCCTCTGGAGGGGA | 10580 |
rs374090670 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432329 | CACACACACACACAC[-/A]CACACCCCCCCCCCC | 10580 |
rs374096784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457623 | GGTTAATAAAAGGCT[A/C]TAGTTAGTCACTGTT | 10580 |
rs374123935 | snp | G/T | | | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414736 | TCGCTGGGATTGTGG[G/T]GACGCAGCCAAGAGG | 10580 |
rs374151333 | in-del | -/CTCT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479958 | TCGGAGACATGCCCA[-/CTCT]CTCTCTCTCTCTCTC | 10580 |
rs374151533 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432143 | GCTATTTCAGTCTGC[A/G]TGAGAGCAGTCTGCA | 10580 |
rs374154811 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510797 | GTGAGACTCTGTCAA[A/T]AATTTTTAAAGTGGA | 10580 |
rs374166149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450798 | TGAGCCACTGTGCCC[A/G]GCTCTGTGGTTATAA | 10580 |
rs374171708 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328549 | CCTTTCATAAGACAG[C/T]TGGGGGGTAATGGCA | 10580 |
rs374192190 | in-del | -/CCCT | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437709 | TTGGTTCCTATGAGG[-/CCCT]CCCTCTGCCGAGAAT | 10580 |
rs374194543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472435 | GACATCTGAATAAAT[C/T]AAGGAGACCGATGTA | 10580 |
rs374203957 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458630 | GGTCAGCTTTCTCCT[-/A]AAAAAAAAAAAAAAA | 10580 |
rs374212313 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415124 | AGAGAAAGAACAGAA[C/G]AGGCAGGCAGGCTGT | 10580 |
rs374214816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499050 | TTGTTGCCACTTCCT[A/G]TGAGTCTATAATGTT | 10580 |
rs374238563 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351681 | TCTTGCTTCTGGCAG[-/C]AAAAGGCCAGGTGAG | 10580 |
rs374250707 | in-del | -/TGTC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378718 | CCCTCTTTTAATATC[-/TGTC]CGTCCTACTACATAT | 10580 |
rs374263982 | snp | C/T | 8.23716e-05 | 0.00641709 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95399134 | GCCAGGTGAGGTGGG[C/T]TTTTCCTGGGTTGGT | 10580 |
rs374286468 | in-del | -/GC | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442526 | TGGCACCCCCCCCCC[-/GC]ACCCTTACTTATGCT | 10580 |
rs374324503 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436902 | GGCACCGCGAGCCCC[A/G]TAGCCAGGCTATCTG | 10580 |
rs374335783 | snp | A/G/T | 0.000307953 | 0.0124049 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341725 | GATGTTTCAATATGT[A/G/T]TAAGATTAAGACACT | 10580 |
rs374347619 | snp | A/C/T | 0.000544857 | 0.0164981 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397308 | AACAAAGGCAAAGAG[A/C/T]AAAATTAAATGACTA | 10580 |
rs374352350 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314767 | TGGACTATGCTTCAG[G/T]TCAGATTACCCAAGA | 10580 |
rs374383811 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350642 | ATTCTTTAGTGAGGC[A/G]CACTACTGCAGCACT | 10580 |
rs374410014 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476019 | CTCTGCATCTACTGC[A/G]CTCCAGGCTCCGTGT | 10580 |
rs374412463 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353449 | TGGACAGGTGCAAGT[C/T]TCTTACTGAGTACTG | 10580 |
rs374423780 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377977 | TCGTTTTACTGTGGA[A/G]GTTAATGCTGTGACA | 10580 |
rs374430795 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313899 | TTCTGATCTGGCCCC[C/T]ACAAAGAACAGACGT | 10580 |
rs374469559 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524228 | ATGTGCGTCCACAAT[A/G]ACAAAGGCATGCCAA | 10580 |
rs374483864 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504466 | CTACCCTGTTACATG[C/T]GCAGACATCTGTCTT | 10580 |
rs374504261 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473893 | TACTTATTTAAAGCA[A/G]ATTCAAAAACAAATT | 10580 |
rs374515385 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552305 | TACTTGGGAGGCTAA[A/G]GCACGAGAATCGCTT | 10580 |
rs374529566 | snp | A/C | 0.000148377 | 0.00861198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441076 | GTGGGAAATCTGGGT[A/C]AACTGCCCAGTTTGG | 10580 |
rs374533649 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560906 | ACCCATTCGGGCTTT[C/G]ATGTCTCCTCCACCC | 10580 |
rs374541141 | snp | A/G | 0.000216596 | 0.0104044 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341542 | TCAGGCTTTTCCTTA[A/G]AAAGAAAAGAGGCTG | 10580 |
rs374545902 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334905 | GCCCTCCACAGCAGC[A/G]GGTGACCCCACATAT | 10580 |
rs374557729 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317430 | TAATTCTTATCTTAC[A/G]GGGCTGTTTGTTGAG | 10580 |
rs374562076 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547936 | CCAAGAAAATACCAG[A/G]GCCCAGCTGGGCTTC | 10580 |
rs374583184 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535220 | ATGAAGAAGAGACCA[C/T]TTCATCCAAAGTGCC | 10580 |
rs374596585 | snp | A/G | 0.000176947 | 0.00940438 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414879 | TGTGGAAATAAGGGG[A/G]TCGTTATGGAAAGGG | 10580 |
rs374614748 | in-del | -/AAAAAAAAAAAAAAA | 0.413083 | 0.189483 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528919 | GCAAGACTCAGTCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 10580 |
rs374623736 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552266 | AATTAGCTGGGCGTG[G/T]TGGCATGCGCCTGTA | 10580 |
rs374646573 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406060 | ATATCGGGCGGTGAC[A/C/T]GGAAGACGGTTTCAA | 10580 |
rs374718532 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534354 | TGATCCGCCCTCCTC[A/G]GCCTCCCAAAGTCCT | 10580 |
rs374719243 | in-del | -/GT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330117 | GATGCAAAACTGTGT[-/GT]CACTCTCCTCCCCAA | 10580 |
rs374720670 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496479 | CTGTCCTCCTCCTGC[A/G]TCCATTGGCAAAGGA | 10580 |
rs374739119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386978 | AAAATTAGCCATGCA[C/T]GGCAGCACACACCTG | 10580 |
rs374739868 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449650 | GAGAAGGGGCAGATC[G/T]GGAGCTAGAACATTC | 10580 |
rs374794372 | in-del | -/ACCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435698 | TGTCTGGGAACAAGA[-/ACCC]CCGCCACTGCAAAGT | 10580 |
rs374797329 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522544 | ATCATTCATATGGGT[A/G]CAAAATACTGATAAT | 10580 |
rs374804745 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408839 | CTGATGCTTCCTGCC[C/G]CACCTGCTTAGTGAA | 10580 |
rs374823029 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459610 | GCCCTTCCTTGGAGT[C/T]ACCCAGCAGTCAGCA | 10580 |
rs374829905 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432333 | CACACACACACACAC[-/A]CCCCCCCCCCCCAAG | 10580 |
rs374834788 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541424 | TTTCTCTCATCCAAG[A/T]CCAGAACCCTTCCGT | 10580 |
rs374848332 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433417 | GCAGGAAATCAGTCA[C/T]GGAGGCAGGGAACCA | 10580 |
rs374851188 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463278 | AGTGGTCTTATAATC[A/C]AACGCACAGAGGGTG | 10580 |
rs374886145 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476204 | GATGCCAATAACGAC[A/G]ATGATGACAGAAATA | 10580 |
rs374908972 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419457 | GATCATTTTGATTTG[A/C]GCTCAGATTTACTTT | 10580 |
rs374915389 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349811 | CCCTCTTTTCACTAT[C/T]TCTTCTTCCCAGACA | 10580 |
rs374921607 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95546578 | TGAGGACAGTACCAA[C/T]AGGATGATACTAAAC | 10580 |
rs374926834 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312441 | TTTACCCGGAAGCAT[A/G]GCTAATATATCAAAA | 10580 |
rs374939159 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384182 | AGGGCAATTATCTTC[C/T]CTCATCCACCACTTT | 10580 |
rs374961471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386776 | AAGTTGGAGTTGGGG[A/G]ATGCAGGTAACAGAG | 10580 |
rs374977112 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429173 | CCTCATTTTTTTTTT[-/T]CTTTTTGAGATGGAA | 10580 |
rs374990386 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323830 | CCATCTCTACAAAAA[A/G/T]ATACAAAAATTAGCT | 10580 |
rs375019034 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481452 | AGTCGATGATTCCTA[C/T]CTCCTCTGTTCCTGG | 10580 |
rs375047267 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319673 | ACAAGCAAGTGGAGT[C/G]AGTTCTCAAAAACAA | 10580 |
rs375055740 | snp | C/T | 1.65004e-05 | 0.00287227 | missense | SORBS1 | GRCh38.p7 | 10:95399018 | GTCAATATACATACC[C/T]GGAGTGGGATGCCCA | 10580 |
rs375058700 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390819 | GCTAATTTTTTTTTT[G/T]TATTTTTAGTAAAGA | 10580 |
rs375061866 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473902 | AAAGCAAATTCAAAA[A/G]CAAATTAAAACTGTT | 10580 |
rs375069241 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349536 | TGTGTTCATAGCTCA[C/T]TGCAGTCTTGAACTT | 10580 |
rs375072444 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323045 | ATTGGAAACATGGCT[G/T]CAGTGAGGTGAGGAT | 10580 |
rs375073899 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466796 | GGATATCGCAGATTT[-/C]TTTTTTTTTTTTTTT | 10580 |
rs375078431 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327686 | CTGGCCCCAAATCCC[C/T]TCTAGAAACAGCACG | 10580 |
rs375090664 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411130 | TGCAATTCCAAATGC[A/G]ATCCAAGAACAAGAG | 10580 |
rs375096221 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431241 | ATCCCCTACAGCAGC[A/T]GCTCTCAGATGCAGT | 10580 |
rs375129455 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488600 | CCCCAGCCAACTCTA[C/T]ATCTTTATGAGAATA | 10580 |
rs375145549 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398972 | TGTACACTTGTCACA[G/T]CTTAAGATGAAGCCT | 10580 |
rs375153403 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95375988 | CGGTTTCCCAAACTC[C/T]AATTCCGAAAAGAAT | 10580 |
rs375167778 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406053 | TGATTGAATATCGGG[C/T]GGTGACCGGAAGACG | 10580 |
rs375172219 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413058 | GATTTCTGCATGACT[C/G]GCTTCAGCTTAACAA | 10580 |
rs375184210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491179 | ACCCTGTGGCCTCTC[C/T]CCAACAGGACTCATT | 10580 |
rs375184315 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504470 | CCTGTTACATGTGCA[C/G]ACATCTGTCTTCAAG | 10580 |
rs375188123 | snp | A/G | 4.97938e-05 | 0.00498943 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371962 | CACACACAGTCCAAC[A/G]GAGGAGGCACAGCGG | 10580 |
rs375192457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407200 | CACATGGATGAGGTT[C/T]GTACTGGCTGAACAT | 10580 |
rs375233748 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384321 | TAGTCAGGAGAAGTC[C/T]GGCTAAGGTAAGAGA | 10580 |
rs375276204 | snp | C/T | 8.31138e-05 | 0.00644593 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394720 | CTATCCACCAGGAAG[C/T]AGAGGAAGTGACAAA | 10580 |
rs375282216 | snp | C/T | 4.96504e-05 | 0.00498224 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434602 | ACAGTTAGAGAAAAT[C/T]GACCGACCCAAGGAG | 10580 |
rs375291668 | snp | C/G/T | 0.000230626 | 0.0107363 | synonymous-codon, missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336761 | TCTTTCGCCTGCCCC[C/G/T]CTCTCTGCTTTCCTC | 10580 |
rs375325651 | snp | C/T | 0.00819845 | 0.0634981 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355481 | GAAGTGCAGCCACTA[C/T]GAGCCATGATTAATT | 10580 |
rs375326848 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351582 | GGAGGCAGCACTTCA[C/T]TGGAAAAGCCGGGAT | 10580 |
rs375335419 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538842 | AAAGCAAGACCCTGT[C/T]TCACAAAAAAATAAA | 10580 |
rs375351594 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470945 | GAGGCAGGAGAATTG[C/T]TTGAACCCAGGAGGC | 10580 |
rs375357595 | in-del | -/CACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365174 | acacacacacacaca[-/CACA]TAAGGTTAGTAAATG | 10580 |
rs375390653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457942 | AGGCTAGAGACTTCA[C/T]CACTATGTAATATAT | 10580 |
rs375398034 | in-del | -/A | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510819 | AAAGTGGAAAAAAAA[-/A]TGAAAGCGAAGATGT | 10580 |
rs375407317 | in-del | -/AGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552985 | TTTGAGAAGTTGAGG[-/AGG]GAGGATTGTTTGAGG | 10580 |
rs375418587 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523026 | GTGTCAGAAATAAAC[A/G]TGTAAACATTTTCTC | 10580 |
rs375423819 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314406 | TGGGCAAACCTTGTG[C/T]GCGTTTCTCTCTGAA | 10580 |
rs375437933 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434243 | AGGTTCTCTGTGAGA[A/C]CAGGTTAATTCTCAG | 10580 |
rs375440911 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502168 | AAAGAGCAATTTCTT[A/G]GAGAACAAAAATTAA | 10580 |
rs375462712 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463361 | GTCCCACTGATGATG[A/G]CTGCTGAGAGAGTGA | 10580 |
rs375480312 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95561244 | GGCGCCGCCCGCGGG[A/G]GCCGAGCCGCGCACA | 10580 |
rs375480967 | snp | C/T | 8.29043e-05 | 0.0064378 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406067 | GCGGTGACCGGAAGA[C/T]GGTTTCAACAGGAAC | 10580 |
rs375497300 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544272 | CTACCACCCTCTGAG[G/T]CAGTGGCTCAGCCCT | 10580 |
rs375513997 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383368 | GTGCAGTGAGCCGAG[A/G]TCACACCACTGTACT | 10580 |
rs375518419 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492164 | CTAAAATGCTTGCCA[A/T]ACATCAAAAGTGCTC | 10580 |
rs375530518 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509629 | CTTCCTCAAAAAAAA[A/G]GAAGAAAAAAAAAAA | 10580 |
rs375532214 | snp | C/T | 3.41559e-05 | 0.00413241 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432412 | CTCCCGCCCTTCCCA[C/T]GTGGCTTTGAACAGC | 10580 |
rs375533326 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453178 | GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGGCAT | 10580 |
rs375534089 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417334 | TCGAGATGGAATCTC[A/G]CTCTGTCACCCAGGC | 10580 |
rs375547211 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95341912 | ATTGACTAGCCCTTG[A/C]AAGTGCTCAGAGGCC | 10580 |
rs375550485 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388302 | TCTATTAATAGTTGC[G/T]GTTCCTTGCTGCCTT | 10580 |
rs375551325 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494589 | GAAATCTCTTCCCCC[A/C]ATATTACAAGGTGCC | 10580 |
rs375609444 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552140 | ACGCAGTGGCTCACA[A/C]CCGTAATCCCAGCAT | 10580 |
rs375622600 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521481 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 10580 |
rs375625060 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438750 | CATGTTCTTCCTTTC[-/T]TTTAATTAAATGTAA | 10580 |
rs375629688 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333749 | CCAGCCTGGGTGACA[C/G]AGTGAGACCCTGTCT | 10580 |
rs375640980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446986 | TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC | 10580 |
rs375675430 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318232 | TTCTTTCTGTGCAGA[A/G]GAGATTGCTTTGCTT | 10580 |
rs375679952 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416673 | TTCATTCTTTTCCTT[A/T]AGGAAAAGGAGAACT | 10580 |
rs375685794 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427159 | GACTGGAGCCAACTG[A/G]TACAGAATTAACAAA | 10580 |
rs375685884 | snp | A/C | 3.30093e-05 | 0.00406246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322063 | TGTCAGAAGGGGATA[A/C]CTTGTGATGAAAGTC | 10580 |
rs375692421 | snp | A/G | 6.64938e-05 | 0.00576563 | missense | SORBS1 | GRCh38.p7 | 10:95354899 | CTTTATCATCATGAC[A/G]TCTTCGAATAAATTC | 10580 |
rs375711884 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340756 | CAGTAGAGATGGGGC[C/T]TTGCTACGTTGCTCA | 10580 |
rs375724612 | snp | C/T | 8.28933e-05 | 0.00643737 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95376052 | TCTGGGCTTATATCC[C/T]GACTCTATAGGGGTT | 10580 |
rs375726714 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354190 | CCCATTTGGCTGATA[C/T]GAAGAACTTCCTCTT | 10580 |
rs375764420 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484246 | AAAAGGTTGTTTTGT[G/T]GAACCTAAAGATCTC | 10580 |
rs375780711 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468154 | CACCCGCCTCGGCCT[C/T]ATAAAGTGCTGGTAT | 10580 |
rs375780812 | snp | A/G | 1.75121e-05 | 0.00295901 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336555 | GCAGCTTTCCTCCCC[A/G]CCTGCTCGCCACCTC | 10580 |
rs375805605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377507 | CAGGGAACCTTCTTT[C/T]AACTGAAACCAAGCT | 10580 |
rs375831051 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384899 | TTTGTTTTGATTCCA[C/T]CTCAATCTGGTTCCC | 10580 |
rs375831133 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95550843 | CCCAGCAGATGAGAT[A/G]TGTCAACAGCAGTGG | 10580 |
rs375843984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559649 | GTGCCTTGGGCAAAG[A/G]TGCCAACAGACCAAC | 10580 |
rs375850083 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479658 | GATGGGGAGAGAGGT[C/T]AGATGATCCGTGGCG | 10580 |
rs375856816 | snp | A/G | 8.25771e-05 | 0.00642508 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336634 | GGGGCTTGCCGGGCC[A/G]GCTCTCCTCAGGGGT | 10580 |
rs375858444 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326250 | AGGTGTTCAAAGACA[C/T]TTCCTTATGTAAAAG | 10580 |
rs375860742 | snp | C/T | 0.000153988 | 0.00877328 | missense | SORBS1 | GRCh38.p7 | 10:95381789 | TCTTATCTGGGGGTT[C/T]CCAGTCATTTCTGCA | 10580 |
rs375867336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541941 | TCAGGGCCTAAGCCT[A/G]TTGGCCTCCTGGCTG | 10580 |
rs375874931 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561497 | GAACCGTCCACTCTG[A/G]CAGCGCCCGGCCAGC | 10580 |
rs375875588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315188 | TGAGTTGAGACAGCA[C/T]GCTGCAGAGATTTCT | 10580 |
rs375893693 | snp | C/G | 1.6918e-05 | 0.00290839 | missense | SORBS1 | GRCh38.p7 | 10:95339164 | GCACTGCGACTTGGG[C/G]AGGAGGAGAAAGGCA | 10580 |
rs375901607 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362871 | AGGCAACAGAACGGA[C/T]AAAAAGTTCCAGCCT | 10580 |
rs375912001 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516505 | TTTGAATCTCACAGC[A/G]GTGCTGAAGTAGATA | 10580 |
rs375937475 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534657 | TTAATTCATTTTGGC[-/T]TTTTTTCCCCATTCA | 10580 |
rs375954894 | snp | A/C | 1.64751e-05 | 0.00287007 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336728 | GCTCTTCTTAGAGAT[A/C]TTGGGTCCACCAGGG | 10580 |
rs375959073 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541174 | AGATGAGATGGAACC[A/G]TAAAGGCAGTGACTC | 10580 |
rs375964314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552673 | AATCGAATATGAATG[C/T]AGAATATGAACATTT | 10580 |
rs375977988 | snp | A/G | 0.000363998 | 0.0134858 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422142 | CCCCTGTAACTCCGG[A/G]GTCCTTGGTAGAAGG | 10580 |
rs375980842 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433024 | GAAGTGGGGGCGGTG[G/T]GGGGGGTGGGGGCGG | 10580 |
rs375990240 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | SORBS1 | GRCh38.p7 | 10:95432522 | TCCCTGTAGGAAGAC[A/G]AGGCCCGGAGAGTCA | 10580 |
rs375993446 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445767 | ACGCATCCATGAAAC[C/T]ACACAAATTGAGCTT | 10580 |
rs376008910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401328 | AGTAAGCCATGATCA[C/T]GCCACTACACTCCAG | 10580 |
rs376011043 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558194 | CTCGGGAGGCTGAGG[C/T]AGGAGGACTGCCTGG | 10580 |
rs376053157 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493792 | ACACCTGCAGAACTA[C/G]AGCAACAAAATAACC | 10580 |
rs376057189 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494863 | TTTTTATTTTTATTT[A/G]TTTATTTATTTATTT | 10580 |
rs376067035 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553204 | GTGGACAGAGCAAGG[A/C]CCTATCTCAATAAAT | 10580 |
rs376076588 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351508 | CTCAGCTGTCAGAAC[A/G]GCTGTAGAGCCACAA | 10580 |
rs376108112 | in-del | -/TTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404500 | GTTTACACGTGTGGC[-/TTTT]TTTTTTTTTTTTTTA | 10580 |
rs376121848 | snp | A/T | 1.78525e-05 | 0.00298763 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337018 | GTGGAGAAGCTACTG[A/T]TCGTGGGGTGGGACG | 10580 |
rs376127191 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364442 | ATTGTGTGTGTGTGG[-/G]GGGGGGGTGTTTGCT | 10580 |
rs376144048 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95437542 | CATCACAGCTTTGGA[A/G]CCACCATCACATTCT | 10580 |
rs376153386 | snp | A/G | 0.000411953 | 0.014346 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336890 | CAGCTGCAAGAAGCT[A/G]TCTTGGTGGATGCCT | 10580 |
rs376166685 | snp | A/G | 3.31208e-05 | 0.00406931 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95434710 | TGCGCGTAAAGGGTC[A/G]GCAGTTGCTGAAAAC | 10580 |
rs376183934 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454513 | TACAGGTCCTGGCTC[C/T]GGCTCCTCAACCCAG | 10580 |
rs376187324 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523870 | GCAACACCAAAATGT[C/T]AGCAGGGATAACACT | 10580 |
rs376215285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344411 | ATTCCATAACATGCT[A/T]TTTTTTTTTTTAGAT | 10580 |
rs376225823 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555629 | CACTTTAGATACTAA[A/C]GTACTTGCTGACCAC | 10580 |
rs376226107 | in-del | -/AC | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391079 | AGGGGACAAGCAAGA[-/AC]ACAGAGTCAGGAAGG | 10580 |
rs376234086 | snp | A/C/T | 0.000132317 | 0.00813289 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406096 | ACAGGGATTAACACA[A/C/T]AAATAAATATTTCTC | 10580 |
rs376239481 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529552 | AAATGCAGAACCCCA[A/G]GCCCAGCCCCTAAAA | 10580 |
rs376247924 | in-del | -/TC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490105 | TACCTGGAGGCACTC[-/TC]ACCTCAGCACTGGAA | 10580 |
rs376288523 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393151 | ACTGCGCTCTCTACA[C/G]CAAATAGACTCTTCT | 10580 |
rs376308016 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524434 | TACTACCCCACTGAC[C/G]GTACATCACTCCCTC | 10580 |
rs376311091 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395544 | AGCACCTACAATTTA[C/G]ATTAAGAACTATAAC | 10580 |
rs376317084 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510794 | ACAGTGAGACTCTGT[A/C]AAAAATTTTTAAAGT | 10580 |
rs376320905 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465728 | TATCATTGAATCTTC[C/T]TATGGGCAAAAAGGC | 10580 |
rs376326801 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482549 | AATTTCCTCTCAGTG[C/T]GGCAAGTTCAGGATA | 10580 |
rs376332734 | snp | A/G | 3.30322e-05 | 0.00406387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321936 | CCTCTGAGAACATGA[A/G]AATCGAAGTTCACCA | 10580 |
rs376365153 | snp | A/C | 1.671e-05 | 0.00289045 | missense | SORBS1 | GRCh38.p7 | 10:95381688 | TATGCACATTACCAT[A/C]TTTTCGTTGGTCAGA | 10580 |
rs376367649 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364046 | TTTACAGATCCATCC[A/G]TTCATTGAGCAAACA | 10580 |
rs376386982 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551167 | GGTAACTTACACCAG[A/G]GATACAGCCAAGGGA | 10580 |
rs376404698 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332818 | AGGTATCACGGTCCC[A/G]CCTTTGGAGCACTGA | 10580 |
rs376409231 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338113 | GCCAACCTCCTTACA[A/T]CATACATGGTGGTTT | 10580 |
rs376510178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359084 | ATGCTTTTACATTCC[A/G]GGAAACTGGCCTTTC | 10580 |
rs376512304 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391149 | AAAGCCTGTGTTAAT[A/G]GAGCCCCAAACACCT | 10580 |
rs376516963 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413239 | CTACCAAGTGAGATT[C/G]CTAGGCTCTTCTCCA | 10580 |
rs376533116 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434575 | AAAGGAAAACCATGC[C/T]ATGATCCGCTCACAG | 10580 |
rs376540630 | snp | C/T | 0.000364184 | 0.0134892 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346493 | TAAAATCAGGATTCA[C/T]GGACAACAAGGACAC | 10580 |
rs376551293 | snp | G/T | 6.59098e-05 | 0.00574026 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410627 | TGGGGCACAAGCCTC[G/T]CTTACCTCGATTGTG | 10580 |
rs376595292 | in-del | -/ACACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432329 | CACACACACACACAC[-/ACACAC]CCCCCCCCCCCAAGA | 10580 |
rs376633968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457387 | CTAGGTGCTCAGGCA[A/G]TGACGCTACCACTGT | 10580 |
rs376649142 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314541 | TTTGGTCTTGGGCAG[C/T]GTGGGGGACTCCACC | 10580 |
rs376653678 | snp | C/T | 1.65589e-05 | 0.00287736 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371342 | TGTGGCACGTTTGCA[C/T]TGGGTGCTTTATTAA | 10580 |
rs376666289 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336831 | CTCTGGCTGCTAAAG[A/G]CATCACTAAGCTGGG | 10580 |
rs376688416 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532432 | AATGGGATCCCCTTT[A/C]AGTCAACAGTGATTG | 10580 |
rs376688489 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513330 | AGCAAAGAGCCAATC[C/T]TGGCTCCAATCAGCA | 10580 |
rs376717583 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458330 | TCAAATATTTCTAAA[C/T]TGCTTTTAAAATTTC | 10580 |
rs376752664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461277 | TCACTCATAAGTAAA[A/C]ATATGGACCCAAAAT | 10580 |
rs376759418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415121 | GAGAGAGAAAGAACA[A/G]AACAGGCAGGCAGGC | 10580 |
rs376759877 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410444 | GATATCACCTCAGAT[A/C]AGGGGCCTCTGTCTG | 10580 |
rs376773859 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458879 | TGGGGGAAAGGATAA[A/G]GGTCCCATACAAGAA | 10580 |
rs376776479 | snp | A/C/G | 0.000329847 | 0.0128383 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414710 | GGTCAGAGGTGAGGC[A/C/G]GCAGAGGCAGTCGCT | 10580 |
rs376780385 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364622 | GCCCAGCTAATTTTT[A/G]AAGTATTTTTTGTAA | 10580 |
rs376785204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495235 | CCTACAGTACTGTTA[C/T]ATTCTGGCCTAAAAC | 10580 |
rs376799173 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523528 | AACATTCCAACCACA[A/G]TATTATTTTAGGACA | 10580 |
rs376802238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409242 | TTCTGTTTGACTGAA[A/T]TTTTTTTTTTTTAAA | 10580 |
rs376816355 | snp | C/T | 1.66665e-05 | 0.00288669 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318436 | TGATAGCTAAATCTA[C/T]ACATGAAAAAAATGA | 10580 |
rs376872212 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397216 | TACAAATGAAAATCA[A/G]TACCTCTGTTCAGTT | 10580 |
rs376873391 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442228 | AAGCAACTGGTTAGA[C/T]ATGGCTGGGTCAATT | 10580 |
rs376877117 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560680 | CACGGGCGGCACGGG[-/G]CAGGCGCCGTGTCCC | 10580 |
rs376877381 | snp | A/G | 3.70906e-05 | 0.00430627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414905 | AAGGGGTATGATACG[A/G]GGAAAGAATTCCATA | 10580 |
rs376880650 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457203 | CAAAATGGCCTTGTC[A/G]CCACAATTCACAACT | 10580 |
rs376884770 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343977 | TTTGGGGGGCATTAC[A/G]AATTCCCCCTCCCTT | 10580 |
rs376901108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552263 | AAAAATTAGCTGGGC[A/G]TGGTGGCATGCGCCT | 10580 |
rs376926454 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319015 | ACCCCTGCTTTAAAG[C/T]AAACTAAGCCTTTTC | 10580 |
rs376968108 | snp | C/T | 0.000157186 | 0.00886389 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337236 | TCGGGGGACAGGGCT[C/T]GGCGGGAGTGGGGCA | 10580 |
rs376972020 | snp | A/G | 3.30289e-05 | 0.00406366 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394990 | AGATATGCTGTCTAA[A/G]TTTATGGTACCTTCG | 10580 |
rs376993697 | snp | C/T | 0.00018143 | 0.00952271 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414784 | GTCTGGCAGTGCCTT[C/T]TTGCCCTCTGTCAGT | 10580 |
rs377009279 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454903 | ACACCCAGGCACATG[C/G]TGACAAAAGCACCAA | 10580 |
rs377022773 | snp | C/T | 3.30529e-05 | 0.00406514 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95341591 | GCGTGGGAAGATTCC[C/T]ACCCGGCCGTGGTGT | 10580 |
rs377028263 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408166 | GTTCTCAATGTGGTC[A/G]GTGGGCCAGTGGCAC | 10580 |
rs377030734 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541630 | TCCTCTATCCCACTG[C/G]ATCAATCCTGTCCTG | 10580 |
rs377032716 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464931 | GAAAAGGAAAAAGTC[G/T]ACCCACAAACTCAGA | 10580 |
rs377036973 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313179 | TAACTCATTCCTATT[A/G]TCAATCATTTACACC | 10580 |
rs377037281 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361541 | ACCTCCGCCTCCCAC[A/G]TTCAAGTGATTCTCC | 10580 |
rs377037673 | snp | A/G/T | 1.65954e-05 | 0.00288053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341553 | CTTAGAAAGAAAAGA[A/G/T]GCTGCGGTACCTCGA | 10580 |
rs377037783 | in-del | -/TCA | 0.00914312 | 0.0669923 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500727 | GACTCAAGGAGACAC[-/TCA]TCATTCTAGAGTGGG | 10580 |
rs377044601 | in-del | -/CAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500731 | CAAGGAGACACTCAT[-/CAT]TCTAGAGTGGGGATT | 10580 |
rs377059260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508025 | AGAGTCACACCCTGT[C/T]GCCCAGGCTGGAGTG | 10580 |
rs377062252 | in-del | -/ACC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384687 | TGTACGGTTAAGCTC[-/ACC]GAGTTCAACAGTGTC | 10580 |
rs377063819 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495026 | GAGTAGCTGGGACTA[C/G]AGGCGCCTGTCGCCA | 10580 |
rs377067122 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449698 | ATCATTTTTTTTTTT[-/T]ACCTTTTATACTTGA | 10580 |
rs377072946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483517 | AAACACACAAATTCC[A/G]TTCTTTCTTTTTTTT | 10580 |
rs377081882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455594 | ATCACTTCATTTACA[C/T]GTAAAACTTTTTTTT | 10580 |
rs377103614 | snp | C/T | 3.3232e-05 | 0.00407614 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336598 | TCTGCTCAGCCTCAC[C/T]TCCTGGAAAAGCGCT | 10580 |
rs377104804 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418211 | GCCTCCTGAGTAGCC[A/G]AGACTATAGGCCTGT | 10580 |
rs377111968 | snp | C/G | 1.65083e-05 | 0.00287296 | missense | SORBS1 | GRCh38.p7 | 10:95432478 | GTTGCCGGGTTTCCT[C/G]AGGGCTCGCAGGGCT | 10580 |
rs377121828 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506048 | TAACATGTTGATTTA[C/T]TGCTGCCAATCTCTC | 10580 |
rs377126111 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477026 | TGACTCCAAAAGAGA[A/G]CACACTCCCAACACC | 10580 |
rs377126363 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498907 | CAAATGAGTACATAT[A/G]ACACAAATGATATCT | 10580 |
rs377128678 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423597 | AAAGAGGGACTAACA[C/T]TGCAGTCTCACTGCC | 10580 |
rs377131392 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324204 | ATCAAGTGTGCTCAC[C/T]GACCTCATCTTCAGT | 10580 |
rs377133449 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480760 | CTGGGTACGAGGCAC[A/G]ATCTTGCACCCAAGG | 10580 |
rs377173235 | in-del | -/CC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388831 | AGCTCGATTTGGGGA[-/CC]CAGCCACTCTCCTAC | 10580 |
rs377181734 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395132 | TACAAATGGAGAGAA[C/T]AAACGAGTAGGAATC | 10580 |
rs377190287 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483237 | TCCAGTTTTATATTT[C/T]TGTCTATTAAAAGGA | 10580 |
rs377197590 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417645 | TTTTTTTTTTGAGAC[A/G]TAGTCCCACTCTGTC | 10580 |
rs377199841 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493627 | AAGCAGCACACAGAG[A/G]AGTAAAGACCAAACA | 10580 |
rs377236017 | snp | A/G | 3.52833e-05 | 0.00420005 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337174 | GAGAACGCCTGCCTG[A/G]GACCCCCACAGTCAG | 10580 |
rs377246817 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452593 | AAGATAAAACCACTA[A/G]AACATTCAACATAAT | 10580 |
rs377274867 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318537 | TTTTCAGCAGTGTTT[C/T]CTACTTATCAGTAGG | 10580 |
rs377306204 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445525 | ACCCAAGATCTTGCC[A/G]ATAAATCCCTCTTCA | 10580 |
rs377306582 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361075 | CACCTTGACCTCCCA[A/C]AGTGCTGGGATTACA | 10580 |
rs377311360 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540255 | GGGTGGCAGCCGCAG[C/G]CGCGTTTTAGGTAAG | 10580 |
rs377321232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468231 | AGGTGTTAGGCTAAA[A/G]AGACTTCACTGGAAC | 10580 |
rs377334870 | snp | G/T | 1.64757e-05 | 0.00287012 | missense | SORBS1 | GRCh38.p7 | 10:95399137 | AGGTGAGGTGGGTTT[G/T]TCCTGGGTTGGTGCT | 10580 |
rs377350023 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439858 | CTGAGGTCAGGAGTT[C/T]GAGACCTGGTCAACA | 10580 |
rs377380118 | in-del | -/A | 0.0501905 | 0.150254 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527261 | AACCTCGTCCTTACT[-/A]AAAAAAATACAAAAA | 10580 |
rs377381875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392388 | TCAGTGATCTATGCC[C/T]GGATATGTCATCTAG | 10580 |
rs377418322 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322893 | CATGAGCAAATCCAC[A/G]TACCACACCATCACG | 10580 |
rs377420182 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344794 | TGGAGCTAGAATTTA[C/T]TTTTTTCACTAAATT | 10580 |
rs377424635 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554528 | AAATTAGCTGGGGGG[-/G]TGGTGGTCTCCTGTA | 10580 |
rs377444372 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430224 | AGCACTTTGCCAGGC[C/T]GAGGCAGGTGGATCA | 10580 |
rs377454267 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383952 | GAACAACAAGGCCCA[A/G]GCTGAATGAATGAGA | 10580 |
rs377460834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529136 | AATGTAGGAGGCCAA[A/G]AGAGAATGACTCAGA | 10580 |
rs377462786 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513310 | ATTGAGACACCTTTC[A/G]ATCCAGCAAAGAGCC | 10580 |
rs377464546 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525904 | AGAAACGGACAAAAT[G/T]GAGTTTTCTAAAAAG | 10580 |
rs377470606 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432341 | CACACACACCCCCCC[A/C]CCCCAAGAGGTATCT | 10580 |
rs377471065 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509782 | ATATCAAAAGAATCA[A/G]CTAAGATTTTAAAGT | 10580 |
rs377482536 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95399098 | CCTACTGTCATCCTT[G/T]GCTCTTTTTTCAATA | 10580 |
rs377554057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560890 | TCACTTTACAGCACA[A/C]ACCCATTCGGGCTTT | 10580 |
rs377561028 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326277 | AAAGATACGGTGTAC[A/G]GTAATAGCGTCCAAT | 10580 |
rs377564872 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349809 | TTCCCTCTTTTCACT[A/T]TCTCTTCTTCCCAGA | 10580 |
rs377593625 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553103 | CTGTAGTCCTAGCTA[A/C]TCAGGAGGCTGAGGC | 10580 |
rs377594938 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556896 | CATGAAATTTTAATG[G/T]CAATAGATTAAAAGA | 10580 |
rs377596393 | snp | A/G | 5.51445e-05 | 0.00525064 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414528 | GTGAGGTCAGGCTCC[A/G]AGACTCTGCGGAGGT | 10580 |
rs377598514 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533567 | CAGAAAGAACAGATG[A/G]GGACAACCAAAAGGG | 10580 |
rs377607717 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555127 | ACCTCAGGTGATCCA[C/T]CTGCCTCGGCCTCCC | 10580 |
rs377637504 | snp | C/G | 1.65334e-05 | 0.00287514 | missense | SORBS1 | GRCh38.p7 | 10:95383994 | ACTTACCTTTCTGAG[C/G]TTGACTTCAGTGAGG | 10580 |
rs377643638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407839 | CCAACTACTGGCATC[A/G]AGAGGCTGAGGTGGG | 10580 |
rs377656102 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356784 | TCCCGTCGGGAGCGC[A/G]TGAGCAGGTTCTCAA | 10580 |
rs377658070 | snp | C/T | 1.66136e-05 | 0.00288211 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336931 | TGTGGACACCACCGT[C/T]TCCATTCATGTGAAG | 10580 |
rs377660391 | snp | A/T | 1.64833e-05 | 0.00287078 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397215 | CTACAAATGAAAATC[A/T]GTACCTCTGTTCAGT | 10580 |
rs377661830 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437471 | AGTACCAATCCAGAT[G/T]TCTCTCCAAGAACCT | 10580 |
rs377675180 | in-del | -/A | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442515 | TTAAAAGTATGTGGC[-/A]CCCCCCCCCCGCACC | 10580 |
rs377689861 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387771 | TTATTATGGAAGAGG[A/C]AGAGAAAGATGCTGT | 10580 |
rs377693980 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332695 | TGACCTCAAGTGATC[C/T]GCCTGCCTCAGGCTC | 10580 |
rs377694197 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420499 | CAGGCAGCACATTTA[G/T]ACACTGTGAAAGGGT | 10580 |
rs377744487 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477042 | CACACTCCCAACACC[C/G]AGCTGCAGAAAAGTG | 10580 |
rs377757885 | snp | C/G | 3.29571e-05 | 0.00405924 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437572 | TGCAAGAAAGAAAGA[C/G]AGCATGAGGTTTGTG | 10580 |
rs386372150 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413999 | AAAAAAAAAAAAAAA[-/AA]ATCCTAGTCTCTGTC | 10580 |
rs386372151 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494081 | CTTTTAAATAAATGT[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs386372152 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510812 | AATTTTTAAAGTGGA[-/A]AAAAAAATGAAAGCG | 10580 |
rs386372153 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510818 | TAAAGTGGAAAAAAA[-/A]ATGAAAGCGAAGATG | 10580 |
rs386372154 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534103 | ATGCAGCTTTTTCCT[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs386372155 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534120 | TTTTTTTTTTTTTTT[-/TT]TGACATGGAGTCTAG | 10580 |
rs386372157 | in-del | -/AAAAA | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562769 | CTCTGCTGTGTATTA[-/AAAAA]AAAAAAAAAAGAAGA | 10580 |
rs386372158 | in-del | -/AAAAA | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562775 | TGTGTATTAAAAAAA[-/AAAAA]AAAAGAAGAGTCCTA | 10580 |
rs386746734 | in-del | AA/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354217 | TCTTCCCAAATCCCC[AA/T]GAAAAGGGGCTCTTT | 10580 |
rs386746735 | in-del | CA/GCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95372790 | CTAAGACAGAAATTT[CA/GCC]AAAAGATTGTTGTAA | 10580 |
rs386746736 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380866 | TATTTTAATAAAAAC[CA/TG]AACTCCAGCATAATA | 10580 |
rs386746738 | multinucleotide-polymorphism | AA/GT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397940 | CACAGAGCTGATGAG[AA/GT]GGTGAGTGGAAGGGC | 10580 |
rs386746739 | multinucleotide-polymorphism | GT/TG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418849 | GGCAGAAGGACCACT[GT/TG]AGTCTGAGACCAGCC | 10580 |
rs386746740 | in-del | ACACACCC/CG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432329 | CACACACACACACAC[ACACACCC/CG]CCCCCCCCCAAGAGG | 10580 |
rs386746741 | in-del | ACACCC/CG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432331 | CACACACACACACAC[ACACCC/CG]CCCCCCCCCAAGAGG | 10580 |
rs386746742 | multinucleotide-polymorphism | AT/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453839 | GGCCCGCTGCAGGAC[AT/GC]AAGTCTGCTCAGATT | 10580 |
rs386746743 | multinucleotide-polymorphism | AAC/TCA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461162 | ATTTTAAAATTATTC[AAC/TCA]CATGTGCCCTTCAAC | 10580 |
rs386746744 | in-del | ACATGCAACCTAGA/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488756 | TTTTACTCACATGCC[ACATGCAACCTAGA/T]AGGCTCTACCTTCAA | 10580 |
rs386746745 | multinucleotide-polymorphism | AT/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493096 | AGGAGTTTGAGACCC[AT/GC]CTGACCAACATGGTG | 10580 |
rs386746746 | multinucleotide-polymorphism | ACT/GCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499230 | GGCGTCCACCACCAC[ACT/GCC]CAGCCAATTTTTGTA | 10580 |
rs386746747 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499802 | TGAGGTTTAGACTCC[CA/TG]GACTCTCTTTTGGAC | 10580 |
rs386746748 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505555 | TAGATGAATGTCTAA[CAT/TAC]AAGAGTCAATTCAAA | 10580 |
rs386746749 | multinucleotide-polymorphism | CTT/GTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513754 | GAGCTTAAGATCTCC[CTT/GTG]GGCCACATGGGACCA | 10580 |
rs386746750 | multinucleotide-polymorphism | CT/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536015 | TGAAATAAAATCACT[CT/GC]TCGTCGCACAGCCCT | 10580 |
rs386746751 | multinucleotide-polymorphism | ATT/CTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541232 | GATGAAGGGACTGGC[ATT/CTG]AGGTCTCTCCACTAG | 10580 |
rs386746752 | multinucleotide-polymorphism | CT/TA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558392 | TCCACATCTTGCTAG[CT/TA]GTGCAACCTTGGAAA | 10580 |
rs397711694 | in-del | -/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540256 | GGTGGCAGCCGCAGC[-/C]GCGTTTTAGGTAAGT | 10580 |
rs397725362 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514141 | TCTGAGGGGAAAAAA[-/A]TACATCCTCGGGAGA | 10580 |
rs397729290 | in-del | -/GT/GTGT/GTGTGTGTTT/TA | 0.49753 | 0.0350569 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378764 | TGTGTGTGTGTGTGT[-/GT/GTGT/GTGTGTGTTT/TA]ATGTATGTATGTATA | 10580 |
rs397734908 | in-del | -/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501344 | AGGTGTGACCCACCT[-/T]GTTGAGACACCAGGA | 10580 |
rs397738136 | in-del | -/C | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477083 | GGCCTGAGTCCCCCC[-/C]GGGACAAACCTGAGA | 10580 |
rs397744093 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390818 | GCTAATTTTTTTTTT[-/T]GTATTTTTAGTAAAG | 10580 |
rs397748139 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95402791 | TTTGTATTTTTTTTT[-/T]TATAGAGACGGGGTT | 10580 |
rs397754965 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386652 | TTTTCTTCTTCTTAC[-/T]TTTTTTTTTTCTTTT | 10580 |
rs397757105 | in-del | -/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405456 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTGATA | 10580 |
rs397760859 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319855 | AAACACTTTTTTTTT[-/T]TCATGTTTCTGTATT | 10580 |
rs397771386 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327283 | CACACACACACACAC[-/AC]TGCACTCCCCTCCTT | 10580 |
rs397774620 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554069 | TTTTTTTTTTTTTTT[-/T]GAGAGGGAGTCTGGC | 10580 |
rs397791431 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319856 | AACACTTTTTTTTTT[-/T]CATGTTTCTGTATTT | 10580 |
rs397794456 | in-del | -/CT | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534957 | GCACCATATCTGTCT[-/CT]GTCTCCCGTAGCAAG | 10580 |
rs397803668 | in-del | -/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357426 | AACAAGGTTGGGGGG[-/G]TCAAAGGAACAGAAA | 10580 |
rs397817112 | in-del | -/T | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402792 | TTGTATTTTTTTTTT[-/T]ATAGAGACGGGGTTT | 10580 |
rs397830839 | in-del | -/TT | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353518 | CATTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 10580 |
rs397841684 | in-del | -/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312374 | CATTATTTTTTTTTT[-/T]CTTTTACTGATCCCA | 10580 |
rs397844618 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472145 | AATAATTCACTAAAT[-/T]ATCGAGACATACATA | 10580 |
rs397844714 | in-del | -/A | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312980 | AACAAAAAAAAAAAA[-/A]CAGTGCTCTTAGATG | 10580 |
rs397844944 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475934 | CCAGGATTTGAAACT[-/T]AAGTCTATGTGACTG | 10580 |
rs397845624 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513330 | AGCAAAGAGCCAATC[-/C]TGGCTCCAATCAGCA | 10580 |
rs397845710 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413999 | AAAAAAAAAAAAAAA[-/A]ATCCTAGTCTCTGTC | 10580 |
rs397845986 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361628 | TTTTTTTTTTTTTTT[-/T]GTAGTTTTAGTAGAG | 10580 |
rs397846184 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370268 | TTTTTTTTTTTTTTT[-/T]CCTGAGACGGAGTCT | 10580 |
rs397846649 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414000 | AAAAAAAAAAAAAAA[-/A]TCCTAGTCTCTGTCA | 10580 |
rs397846797 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322407 | TATTAAAAAAAAAAA[-/A]GGCAGCAGCATAAAA | 10580 |
rs397846960 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473048 | AAAAAAAAAAAAAAA[-/A]GTAAACGAAGAAACT | 10580 |
rs397847041 | in-del | -/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442525 | GTGGCACCCCCCCCC[-/C]GCACCCTTACTTATG | 10580 |
rs397847846 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357288 | CAACAACAAAAAAAA[-/A]TGGCTACCCTGCTAG | 10580 |
rs397933888 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433030 | GGGCGGTGGGGGGGG[-/G]TGGGGGCGGGTGGTC | 10580 |
rs397949446 | in-del | -/CACACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503015 | ACACACACACACACA[-/CACACA]AACACTCTGACCATC | 10580 |
rs397954636 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355129 | AAAATTCCACCCCCC[-/C]ACCCCATTTTTTGGA | 10580 |
rs397959493 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316463 | TCTCAAAAAAAAAAA[-/A]GAAGCAAGTGAAGAG | 10580 |
rs397959852 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389586 | GAATGCAAAAAAAAA[-/A]GACCAGGATAGGGTG | 10580 |
rs397961732 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514083 | TAATTTTTTTTTTTT[-/T]ACACAATCTTGAACA | 10580 |
rs397966521 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343303 | TCTTTTTTTTTTTTT[-/TT]GAGACAGAGTTTCGC | 10580 |
rs398014510 | in-del | -/TT | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392282 | TTTTTGGTTTTGAGG[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs398014512 | in-del | -/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490341 | GATTTCCATTCTCTC[-/T]TTTTTTTTTCCCTTC | 10580 |
rs398014513 | in-del | -/A | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508004 | GTGTGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10580 |
rs398014514 | in-del | -/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509629 | TTTTTTTTTTTCTTC[-/T]TTTTTTTTGAGGAAG | 10580 |
rs398046183 | in-del | -/A | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507925 | AAAAAAAAAAAAAAA[-/A]GGAAAGCGAAAGGAA | 10580 |
rs398046184 | in-del | -/G | 0.5 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512798 | ATGAAGATACATGGG[-/G]AAAAAAAAAAAAAGG | 10580 |
rs398075429 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386265 | TTTTGTTTTTTTTTT[-/T]TAAGCCTGAGCTCTT | 10580 |
rs398097157 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315973 | TAAAGCTTAGGAAAC[-/C]TAAAACATCTAGTTG | 10580 |
rs527248066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547696 | ATTGCATGCCAGCAT[A/G]GGTGACAAGAGCAAA | 10580 |
rs527269711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351503 | TAAGACTCAGCTGTC[A/G]GAACGGCTGTAGAGC | 10580 |
rs527277062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357858 | AAAAATAAAGATAAG[A/G]ATAGGAGTTAGTGCT | 10580 |
rs527297121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528056 | TTTAAAAGTCCATTC[C/T]TCTAACAGCCACTTT | 10580 |
rs527313289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554013 | GGAATGAGCCACTGC[A/G]CCCAGGCAGCCTTTA | 10580 |
rs527315362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352225 | TTTCTATTTTTAAAG[A/G]CTTCTTTGAAAAATC | 10580 |
rs527321820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324646 | GGGTGACTGGGAGCC[A/G]ACCTTGTATGGCTCC | 10580 |
rs527345313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363178 | TTTACCCCACTGGAC[C/T]CTGGTTATTTACAAA | 10580 |
rs527361163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407064 | TTGCCAACCCGTGGG[C/T]ACTGTCATCATTCCC | 10580 |
rs527384105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315406 | CCCACTGCTTAGTAA[C/G]TATCAGAGGCAGAAT | 10580 |
rs527388532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541173 | GAGATGAGATGGAAC[C/T]GTAAAGGCAGTGACT | 10580 |
rs527416142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456042 | CACATAGGTAATGTT[C/T]AGAACATAGCACAGA | 10580 |
rs527426134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407482 | AAATTAGCCAGGCGT[A/G]GTGGCACACGCCTAT | 10580 |
rs527431525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492126 | AAAGTCAAGGAAATA[C/G]AGTTGAAGCACCCCA | 10580 |
rs527438310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338320 | ATCCTTTCAGCCCAC[A/G]GAGACTGAGATGCTG | 10580 |
rs527443705 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375675 | TGAAATAATGCCATC[C/G]GCAAGGCATGTGGTA | 10580 |
rs527446150 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544797 | ACAATGATGCTTCAG[G/T]TGAGTATTTAAATAG | 10580 |
rs527452477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436275 | TCCCCATGCTCCTCA[C/G]TGGATGCTAAACACA | 10580 |
rs527460038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527374 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 10580 |
rs527492455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386550 | CTAAGGCAGAAGAAT[G/T]GCTTGAACCCCAGAG | 10580 |
rs527500479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484496 | ATCAAATTATGTAAG[A/G]TTTTCTGATTTTTAA | 10580 |
rs527513687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422425 | TGACCTTTGAAAACA[C/G]AAGGCTCACATTCAC | 10580 |
rs527524325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338910 | GATGGGGTTTCACCA[C/T]GTTGCCAGGCTGATC | 10580 |
rs527526056 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529421 | AACATTTTATTGTCC[A/G]GTTCCTGTAGACATA | 10580 |
rs527526119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429935 | CTGAATGAATGTATG[C/T]TTATTTGGATTCGAT | 10580 |
rs527526669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330667 | AGATGTCTACCACCA[C/T]GCCCGGCTAATTTTT | 10580 |
rs527542922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521666 | CCCATAATTTTTTTT[C/T]CTTCTGTGAGACAGG | 10580 |
rs527576295 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469992 | GAACCACTGAACTAC[A/G]TCCATCTGTAGGGGT | 10580 |
rs527576815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470088 | GTGAAAACACCTAAA[A/T]GACAAAAGGTTTAAG | 10580 |
rs527583986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477330 | ACCCACCCAGCCCTG[A/C]CCTGGGTGGGAGTCC | 10580 |
rs527605048 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352097 | CACTGGGTGAAATGA[A/C]GCTGAGTTAAAGGGA | 10580 |
rs527606458 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528127 | GGAGAATACAGAGAA[A/G]GCTCATGCCCTTCTC | 10580 |
rs527623249 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501276 | TGTGACCAATATCGG[C/T]AAGACTCCCTGGGGA | 10580 |
rs527635720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555165 | TGGGATTACAGCTAC[C/T]GCGCCCAGCTGAAAG | 10580 |
rs527643131 | snp | A/C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461705 | TAATTTGTACTGATC[A/C/G]CGTCAGAATTGCATT | 10580 |
rs527651761 | in-del | -/G | 0.21845 | 0.248001 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433022 | GGAAGTGGGGGCGGT[-/G]GGGGGGGGTGGGGGC | 10580 |
rs527680585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457161 | CATTTCCAAACTAAC[A/G]AATGTTAAAGAGAAT | 10580 |
rs527685799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317486 | CACAGTGTCTGCTTT[A/G]TAATAGAATCTCAAT | 10580 |
rs527700149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416312 | ACAATTCTTAACACG[C/T]TTTTCAGCACATCCT | 10580 |
rs527715830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470862 | GCGAAACCCTGCCTC[C/T]GCTAAAAATACAAAA | 10580 |
rs527724119 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383701 | ATAATGATAGTCAAT[A/G]TTAATTAAGCCCATA | 10580 |
rs527759307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500902 | TGCTGAGCGCACATA[A/G]AAGAAGAGAGCTGGA | 10580 |
rs527761327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324082 | GACATAGAAAAAGTG[C/G]GAGCCTCCCCTGAGG | 10580 |
rs527774406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555556 | ACTAAAACCAGTACA[C/T]ATATATTACAGAGAA | 10580 |
rs527777707 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503282 | AAATGTCACCACTCA[C/G]ATCAGCTGGGCCCAG | 10580 |
rs527780431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423236 | AATATTTTAGGTTTT[A/G]TGGGCCATATGGTCT | 10580 |
rs527811204 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332113 | TCTCTCACTGAGTGC[C/T]CTGCTGCACCCTTTT | 10580 |
rs527815836 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516133 | CAGCTGGGCCTGGTG[C/G]CTCCAGATCTGGGTA | 10580 |
rs527818343 | snp | C/G/T | 0.000199069 | 0.00997504 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372054 | TTTTTGGGAGGCTGA[C/G/T]GGGAAGCAGAGGAGG | 10580 |
rs527884730 | snp | C/T | 0.000214332 | 0.0103499 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95395044 | TTCAGGGAATTTGTA[C/T]GTAGGGAAATAAGGG | 10580 |
rs527891249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501670 | GGCTGCAATGTGCTA[A/T]GATCGCACCTGTGAA | 10580 |
rs527905624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549197 | GGCAGTCACTAGCCA[A/C]ACGTGCCTACAGAGC | 10580 |
rs527907471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346608 | TTGTCTGACCTTAGT[A/G]GAACACTAGATAAAT | 10580 |
rs527908923 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404637 | TCCCTGATGTAGCCT[C/T]AGAGCCCCGTGCAGT | 10580 |
rs527914655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354228 | CCCCAAGAAAAGGGG[C/T]TCTTTCTCAGGCCCT | 10580 |
rs527929323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437283 | TTTTAATACCTCACA[A/G]TGGGAAAATGGCAGC | 10580 |
rs527945281 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449907 | CAAACAAGATAGACG[G/T]GTTAATATCCTTAAT | 10580 |
rs527950405 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358712 | CACAGACATGCGCGC[A/G]CGCGCGCGCGCACAC | 10580 |
rs527958431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409505 | AACCTTAAGATTTTA[A/G]TGGAAAGATCTGAAG | 10580 |
rs527967661 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431689 | CAGTTCATCAGGGTT[C/G]AGAGACAGTGAATAA | 10580 |
rs527974378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318218 | ATCTGAGAAGGCTCT[C/T]CTTTCTGTGCAGAGG | 10580 |
rs528014481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551214 | AGGTAGAGAGATGGG[A/C]GAGAGGGATGGCAGG | 10580 |
rs528016095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359133 | GCCTCTGAGTCCCCA[C/T]GGTCACTGGTAATGA | 10580 |
rs528016321 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464755 | GACCTCTGAAAACAC[C/T]CAGGTGTGAAATGCT | 10580 |
rs528019159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401580 | CTGGGGGACTACACT[C/T]GGGTGAAAAGGAAGA | 10580 |
rs528029953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332481 | GCTCTGTCACCCAGG[A/C]TGGAGTGCAGTGGCC | 10580 |
rs528036864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494540 | ATGACAGACGGATCG[A/G]AGTAAACCGGCTCCC | 10580 |
rs528039587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340487 | CCTGGTATCAATGGA[A/C]CTGTTTTTTCCACTA | 10580 |
rs528048930 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479590 | TCAAACCAATCAGCC[C/G]CACTCCCAGCATTCA | 10580 |
rs528051803 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431261 | TCAGATGCAGTCCTT[C/G]CACTAGCAGCATCAG | 10580 |
rs528082777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381185 | TTGTCCTCAATATTG[C/T]ACTTGTCAAAAAAGG | 10580 |
rs528107464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478822 | GGCTGCCACTTAGGA[C/T]ATCCCCTAAAGGTCA | 10580 |
rs528112265 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431743 | CAGGTGGTGGGGACA[A/G]GGTGTGCACAGAGAT | 10580 |
rs528114120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333046 | GAGAGCCAGCAAAAA[C/G]AGGTAGCTCTGCAAA | 10580 |
rs528115728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487178 | CATTTGCCATAAACC[A/G]TTGGTCATAGACAGA | 10580 |
rs528118466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536715 | CAGCAGGCACTGTGG[A/G]CACTGACCTTCCTAA | 10580 |
rs528121287 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453649 | AGCCCATTAAGTTGT[A/T]CTTAAGATTAAATTT | 10580 |
rs528121976 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412059 | AAAGTGCCTCACCTT[G/T]ATTCCTCCATTTAGA | 10580 |
rs528130273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529099 | TGGCTCCCATGTTAG[A/G]CAATGCAAATGACCT | 10580 |
rs528152655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516701 | CGCTCCACAGGTATA[C/T]TGGCCACAACAGGGG | 10580 |
rs528161286 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413765 | CGGCTGTGATGGGAA[C/G]TCATTCCCCCACCCA | 10580 |
rs528168411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472239 | TGAATGGAGCGGCAG[C/T]GGTTGGGGTTGGGAG | 10580 |
rs528185264 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363591 | ATGAGTAGTTACCAC[C/T]ACTGATTTATAGATC | 10580 |
rs528185655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437794 | TCGGATGTCATGTCC[C/T]CTGTGTTGGCTGAGA | 10580 |
rs528186636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339712 | TAGATACTTATAATG[C/T]ATCATTATAGAAAAA | 10580 |
rs528222096 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380791 | CCGATGAGGCGGAGG[G/T]AACATAATTTGAGCC | 10580 |
rs528223405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557246 | ACCACTGTTCACAGC[C/T]CTTTAATTGCTCATT | 10580 |
rs528224332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388043 | GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC | 10580 |
rs528227593 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534210 | CCGGGTTCAATCGAC[C/T]CTCCTGCCTCAGCCT | 10580 |
rs528239651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326593 | ACCAGTTTTTTTCAG[A/G]GGACGGAGACATGGC | 10580 |
rs528247485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359864 | CTTGTACCCACCTGG[C/G]GCTAAGGGCTTTATA | 10580 |
rs528248685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418119 | GTCTCACCCTGTTGC[A/G]CAGGCTAGAGTGCAG | 10580 |
rs528285377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488697 | TCAGTGAACGGCAAC[A/G]TCATTCACCTAGCCA | 10580 |
rs528307646 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315285 | CCTATCTTATCTCAC[C/T]TAGGCTGCCAAATAA | 10580 |
rs528320775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473133 | AGACCACCTATCCTA[C/T]AGTAGATGTACAAAA | 10580 |
rs528338536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465420 | GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 10580 |
rs528341399 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435592 | CCTCGTCCTCTCTTT[C/T]AAGGGCAGCACATAA | 10580 |
rs528347854 | snp | A/T | 1.6676e-05 | 0.00288751 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381810 | CATTTCTGCAGAAAG[A/T]AAATTCTATTAGAGC | 10580 |
rs528351001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326089 | AAAGCTGAGCCCTTT[C/G]ACATCTAATCTCCAT | 10580 |
rs528364272 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348358 | TCACCCAGCTGTAGA[A/G]CTGTGTGAACTTTAA | 10580 |
rs528364948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550502 | ATCCTCCACTGCATG[C/G]GGAGAATAGGCAGGA | 10580 |
rs528370822 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430174 | CCTCAAATCCACACA[A/C]GGGGCCGGGCATGGT | 10580 |
rs528372919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417421 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 10580 |
rs528385965 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425505 | ATTTGGCATAAAGCA[G/T]GTGCTTTGCAAAATC | 10580 |
rs528403845 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390199 | CACCACCAGCCTGAA[A/G]TGGTAGAAGAGGCAT | 10580 |
rs528407607 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406948 | ACATCTCCTTTGTGG[-/A]AGTCCTAATGTGTAC | 10580 |
rs528417520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466015 | TAGCTGGACATGCTG[A/G]TGGGTGCCTGTAATC | 10580 |
rs528465183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348278 | AACTAAATGACCAAA[A/G]TTATAAGGATACGAA | 10580 |
rs528470713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446186 | GCTGCTTGGACCTGC[C/T]GTACTTGGTCAAAGT | 10580 |
rs528472974 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493606 | CACTCCAAAACACAG[A/G]CTGGAAAGCAGCACA | 10580 |
rs528489755 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496082 | AGCATGCACCACCAT[A/G]CCCGGCTAATTTTTG | 10580 |
rs528492425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348722 | GACAGAGATAACTGT[A/G]TAAGAGGGAGACTTC | 10580 |
rs528492778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396746 | TTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 10580 |
rs528497173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504349 | TTGGTGCAAGAGGAC[A/G]GGGGAGGACTCTGCA | 10580 |
rs528505724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544255 | AAACAGACCACCCCC[A/G]ACTACCACCCTCTGA | 10580 |
rs528514521 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550914 | TTGTCTGCTCTGCTA[A/C]GTGCAAGCAGAGCAG | 10580 |
rs528524072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452000 | AAACCACAAAATCCC[C/T]GAGGCTATGTATTTA | 10580 |
rs528528095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360399 | GCATCCATACTTTGA[A/G]TTCCTATTCTTCTGC | 10580 |
rs528531825 | snp | A/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442035 | ATACAGCCTTTCCAT[A/C]ACCCCAAAAAGTTCC | 10580 |
rs528532823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439346 | ACCCCCCACCTGAGA[C/G]AGAGATTCTGGGGAG | 10580 |
rs528575700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411691 | ATCAAAGATCAACTC[C/T]TGTGAACGTACCCAC | 10580 |
rs528575742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403839 | TGCTGGGATTACAGG[A/C]ATGAACCACTGCGTC | 10580 |
rs528600776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538091 | CACTGTAGCCTGGGG[C/G]ACAGAGTGAGACTTT | 10580 |
rs528606708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488611 | TCTACATCTTTATGA[A/G]AATATTGAATGAGCA | 10580 |
rs528619989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396250 | CTCTTTCAGCTTGAG[C/T]GGGCTTTGGTGTGTC | 10580 |
rs528624429 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490038 | TCCCTGGCCCATGGT[G/T]GTCCTTTCCCTCAAT | 10580 |
rs528637007 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473870 | CATGGTCAATTTTGT[A/T]TATCACCTACTTATT | 10580 |
rs528647882 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450279 | TGAATGACAATAATG[C/G]TATACATACAGAGAT | 10580 |
rs528650692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375713 | TTAGTGGGGGGAGGT[A/C]TAAGACAAGCAATGA | 10580 |
rs528651018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383374 | TGAGCCGAGATCACA[A/C]CACTGTACTCCAGCC | 10580 |
rs528656210 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395771 | TCACCACTGTGACCA[C/T]GCTCATCCACCCAAC | 10580 |
rs528680510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481221 | CCTGCCCCCAGCCCT[C/T]TCCTTTTGTCCCTGA | 10580 |
rs528680591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489739 | TCAGGTTCTGGGACT[C/G]AGAATGTCACTGTGT | 10580 |
rs528706332 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514743 | AACCAGAAGACCCAT[C/T]ATCATTCATAGAGAA | 10580 |
rs528712944 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362456 | CAGACACATACATTC[A/G]ACCGCCTTCTAGACA | 10580 |
rs528718672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335761 | AAGTCTTTGACTTTC[A/G]CAGTAGTCAACAGCA | 10580 |
rs528734470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427091 | AATTGGACTGCAGGT[C/T]CAAGAATCTTTATGT | 10580 |
rs528738944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531382 | TTCAAAGCCAACAGC[C/T]CTTGAAACCTTTTTG | 10580 |
rs528742099 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315304 | GCTGCCAAATAATGC[G/T]GGGCGGTAAGCAATG | 10580 |
rs528742194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518444 | GAATCTTCTACTACT[A/G]TGTGACCCAGAGTAA | 10580 |
rs528760052 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487039 | AAGGAAAAATCCTCC[C/T]CCTATGATTGCCAGT | 10580 |
rs528768730 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342975 | ACCTCTACCTCCCAG[G/T]TTCAAGCAATTCTCC | 10580 |
rs528799388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525101 | AACAGCCCAGCATTC[C/T]GGGCGAAAAACAAAG | 10580 |
rs528812998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391048 | CAGTCAGATACCAGA[A/G]AGCCTCTGGACAAGA | 10580 |
rs528842831 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492206 | CGGTCTTGAGTACTC[C/T]TTATGCTAGAAAAAT | 10580 |
rs528853591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468015 | CGATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 10580 |
rs528859725 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369242 | GTTCCACATCACCCA[A/G]CGTCCCCATGGGTAG | 10580 |
rs528867877 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559014 | GCTGTCCTGCCTCTG[G/T]TCCAGAGCTTCTCCA | 10580 |
rs528872756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405730 | GCCCATATCTCCCAA[A/C]CCCTGACTCCTCACA | 10580 |
rs528884628 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313943 | GGTAGTGGCAGAATT[G/T]CTGCTTCAGTCTGAA | 10580 |
rs528885553 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433396 | AAAGATCTGAATGCC[-/A]ATCCTGCAGGAAATC | 10580 |
rs528902449 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322607 | GCCTAACATCTCGCT[C/G]TACTACAATAGCCAC | 10580 |
rs528907686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376515 | TTTTATGGGCTAGTA[C/T]AACTTTAGTACTTAT | 10580 |
rs528916036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467352 | TTAGGGGCAGGGAGC[C/T]GGCCCAGCTTCAAAG | 10580 |
rs528922913 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435367 | CTGGGCAGCACCCAA[C/G]TGCACAGCCCAGGAC | 10580 |
rs528931012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558456 | CAGTTTGGCGGGGAA[G/T]GGGGAGGAACATGGC | 10580 |
rs528940352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429238 | ATGATCTCACTCACT[A/G]CAACTTTCACCTCCC | 10580 |
rs528945896 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391065 | GCCTCTGGACAAGAA[G/T]GGGACAAGCAAGAAC | 10580 |
rs528946645 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409903 | ATCGTCTGGAATTTT[A/G]AAGCAGAAGGGTCAA | 10580 |
rs528980716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419948 | AGCTCTGGCAATCAC[C/T]ATATAGACAAGAAGT | 10580 |
rs528988133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513127 | ATTCTGATGGAAAGA[A/C]ATCACCCATAAGTCA | 10580 |
rs528988985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545812 | CCATTTTCCTCCCTG[A/T]CAATTTGTTATAAGC | 10580 |
rs529056418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398868 | GGAAAAGCTGTTGTA[C/T]ACCAAGTCTGGAGCA | 10580 |
rs529060265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350783 | GTTAAGCTAACTTTC[A/G]TAAAGTTTCATTAAC | 10580 |
rs529063722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440804 | CCATGAAGGTGTAAC[A/G]CATATGTCAAATTTT | 10580 |
rs529086846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392123 | AAGAAGGATGTGCAT[A/G]GAGCGCAGGGCCACC | 10580 |
rs529092798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498318 | ATGAAATGTCCAGAA[C/T]AGATAAATCCATAGA | 10580 |
rs529108667 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392466 | TCCAGGGAGGATGTC[-/TT]TTTAGAAACTTGTGT | 10580 |
rs529128911 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485405 | ATAGTGAATGCTGAA[G/T]TATCCAAAGTTCAAC | 10580 |
rs529128951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446840 | TTGAACAAAATGCTG[C/G]TTATGCCTTAGCTTT | 10580 |
rs529132666 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525920 | GAGTTTTCTAAAAAG[G/T]GGGGCTGGAATTTAT | 10580 |
rs529155594 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540509 | GTGTAAAGATAACAA[C/G]ACAAAGATCATGAAA | 10580 |
rs529166952 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314402 | CTCATGGGCAAACCT[C/T]GTGTGCGTTTCTCTC | 10580 |
rs529188727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482857 | ACAGCAGGTTGCTGT[A/G]GAGTTGGTGGCAAGT | 10580 |
rs529199902 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339791 | CATTTGGGGATAAAC[A/C]CTTAATATTTGGCAT | 10580 |
rs529224837 | snp | A/G | 0.000142901 | 0.00845164 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337307 | AAACTTAAAAAGAAG[A/G]AAAGAGAGGAAAACA | 10580 |
rs529241010 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312659 | TTAAAGACGGGCAAA[C/T]TGGTGAGGCATACCT | 10580 |
rs529268156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489361 | TTACCACCTGAAATT[A/G]TATTGTCTATTTAGT | 10580 |
rs529283567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429316 | CAGGCGTGCAACACC[A/G]TGCTTGGCTGATTTT | 10580 |
rs529286121 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514391 | CTGGTTTCACTTAGG[A/G]CCCAGACTTGTCTGG | 10580 |
rs529289126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329628 | GATTTCCCTTCTGAG[C/T]GAGTCAAAGGAAAAT | 10580 |
rs529294041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378181 | AAAAACATCCTTCTG[A/G]ACACAGAGCAGGAAC | 10580 |
rs529304775 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557479 | AGTTTTGCATTTACA[A/G]AAAAACCGGGACTTC | 10580 |
rs529325504 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483708 | TTTTTGTATTTTTAG[C/T]AGAGACGGGATTTCA | 10580 |
rs529329351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475304 | CGATAAATGTGTATA[C/G]GCACACCTGTATCTT | 10580 |
rs529336825 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392611 | TTTGCTTCTAAATTA[G/T]ATGTGATAAGTTATC | 10580 |
rs529351870 | snp | A/C | 2.80422e-05 | 0.00374437 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384386 | TACGAGCATCCAGCC[A/C]CCCTAGGGATCCCAG | 10580 |
rs529357393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434563 | GAAGAAAAGAAGAAA[A/G]GAAAACCATGCCATG | 10580 |
rs529357803 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318991 | GGTGGTAGTGCCTGG[A/G]GATCGGGGACCCCTG | 10580 |
rs529362981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514179 | AGAATGCCGTTTGAA[A/G]TAAGAATCTTTTTTC | 10580 |
rs529383445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344278 | ACTGCTGGTGAGAGG[A/G]TTTGAGAAATATGAT | 10580 |
rs529383671 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314992 | CCTACTGACTCAACT[A/G]AAAAGATCGGTTCAT | 10580 |
rs529391951 | in-del | -/AATCAGA | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319067 | TAGATTATCAAGCAT[-/AATCAGA]AGTTATTTGGGCCCA | 10580 |
rs529403419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476486 | GGTCACCCTAGAGAG[C/G]AAGGACTAGGTTTTA | 10580 |
rs529421003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554177 | CTGCCTCAGCCTCCA[G/T]ATTAACTGGGATTAC | 10580 |
rs529427843 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414750 | GGGACGCAGCCAAGA[A/G]GCCCCAGAGGTGTTG | 10580 |
rs529468408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316474 | AAAAAGAAGCAAGTG[A/T]AGAGTTCAGGGATGC | 10580 |
rs529481912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560533 | CTACCACGTATCAAG[A/G]AAGCCACATCGGAAA | 10580 |
rs529481956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553554 | CATAACATCTAAAAG[C/T]AACCTCTAAGCTGGG | 10580 |
rs529485643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421344 | AGTAACAACAGGAGA[C/G]GGAAGAAAGAAAAGA | 10580 |
rs529496546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469852 | CATACAGCACAGCCA[C/T]GAGCAGGGCTTGTCA | 10580 |
rs529500526 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386438 | GTCAGGAGTTTGAGA[A/C]CAGCCTGACCAACAT | 10580 |
rs529532756 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365351 | CCGTCTTGTGCAGTT[C/T]AGGGGGATGGAGGTG | 10580 |
rs529552916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555027 | GCTGGGACTACAGGC[A/T]TGCGCCACCACGCCC | 10580 |
rs529557505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462519 | TTCACAGTATATGTA[C/T]AGTATTGTCTCATAA | 10580 |
rs529561535 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500033 | CGGGATTTCTTTTCT[C/T]CACTGAAACTATAGT | 10580 |
rs529562260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370387 | AGCTGGGAATACAGA[A/G]GCCTGCCACCATGCC | 10580 |
rs529568930 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363336 | ATGCCTACATGCATA[A/C]AGATTTCTGACACAT | 10580 |
rs529586688 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539828 | TCCCCCTCCTTCCTA[C/T]GCTCTTTCCACCTGT | 10580 |
rs529590758 | snp | A/G | 0.000170224 | 0.00922405 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414454 | CTGCTGGGAGGAGAC[A/G]TTCAGAAAAGCCGTG | 10580 |
rs529598726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547822 | CCTGGGGCTAACATC[A/G]GAGCTCTCTTTCTCC | 10580 |
rs529603741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345244 | TTTTACCCCTATCTC[A/G]CAGATAAAGAAAATT | 10580 |
rs529604171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352876 | CTGTTTCTGTAGCCA[C/T]GGGAATGGAGTGATG | 10580 |
rs529606932 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538397 | TCCATGTCTGACCTG[G/T]AAGAGGGAGCGGAAA | 10580 |
rs529620438 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367835 | CCAGGACCTCTGGAA[C/G]TCAGGGGGGCTGGAA | 10580 |
rs529642870 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539989 | ACCCTCCAGACAAAG[G/T]TTCCCATTGTTGTCT | 10580 |
rs529647865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507751 | CCCATCTCTACTAAA[A/G]ATACAAAAATTAGCT | 10580 |
rs529672521 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445502 | ACCTTCCATAAACTC[C/T]GTGAACTACCCAAGA | 10580 |
rs529695419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436507 | TGGACATACCCTCTA[C/T]GGCTGGTTCCTTTCA | 10580 |
rs529697734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456978 | TTGTCCACAGTGAAG[C/T]TTTTTTTCTGCCCAA | 10580 |
rs529721911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500687 | TTACCTTTGTAGCTC[A/G]TATCATATTTCTACT | 10580 |
rs529728518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485220 | CAGAGCTATCCAGAA[G/T]CACATTTAGCATGGG | 10580 |
rs529755173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449613 | ACTACCAATATCAAA[A/C]TCTCGTTCCAGGTCC | 10580 |
rs529761569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352358 | GGGATTAACTTTCCT[C/T]GTAGGAAAGCATGAA | 10580 |
rs529772420 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536015 | TGAAATAAAATCACT[C/G]CTCGTCGCACAGCCC | 10580 |
rs529783482 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513233 | CGCATGTAACCCAGA[C/T]GGACGGGTATACGCT | 10580 |
rs529790769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399936 | ACATTGTGCTCTGCC[C/T]TGTGGACATGAAGGT | 10580 |
rs529791100 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408585 | AAAAAAAAAGGGGGG[C/G]GGGGGCAGGGAGGGA | 10580 |
rs529799678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493664 | CAAGGGTAGGGTTCC[A/G]GTTCAAGGCCCGTAT | 10580 |
rs529814848 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442438 | TGTTTGGATCATGGG[A/G]GTGGATATCTCATGG | 10580 |
rs529818287 | snp | A/G | | | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95381736 | CTGATATTCGTAAAT[A/G]CTCTTGGGCTCTGCA | 10580 |
rs529821069 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370317 | GGAGTGCAGAGGTGT[A/G]ATCTCAGCTCTGCCT | 10580 |
rs529822342 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496254 | TAAATCACACTGCAT[C/T]ATTTTATTTAAGATG | 10580 |
rs529832804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372189 | AAGCAAGGGGAGTGG[A/G]TGCTGCCTACGGACA | 10580 |
rs529832905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380539 | TATCTTCTAACAGCA[C/G]AGAACCTCCAAAGAA | 10580 |
rs529838716 | in-del | -/TAAA | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365924 | TTTTGATCACTACCC[-/TAAA]TAGATTAAATTTTTC | 10580 |
rs529861027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477440 | TAACACAGCCCTGTA[C/T]GGTTATGCCTGGGAG | 10580 |
rs529871325 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339592 | CCCTAAGCCAGGGAA[A/C]AAATGTAGTGTTTTT | 10580 |
rs529879856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430395 | AGGCCGAGGCTGCAG[A/C]AAACCATGATTACAT | 10580 |
rs529901321 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416362 | TATCCACAATTCTAA[A/G]TGAAGCCAAAGACTG | 10580 |
rs529908619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528914 | ACAGAGCAAGACTCA[A/G]TCTCAAAAAAAAAAA | 10580 |
rs529914929 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516193 | CAGCAGCATTGCCTG[C/G]GAACCTGTTAGAAAT | 10580 |
rs529922494 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486091 | CCCCAATAGCACACA[A/C]TCCAAACAGCAGTGT | 10580 |
rs529922812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324669 | ATGGCTCCAACACCA[C/T]CCACCCTCCACTCAC | 10580 |
rs529935975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471414 | GTGGAGAGGAGGAAC[A/G]CTGAGGTTAGGGTGG | 10580 |
rs529941330 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562704 | AACTCATCAGCAAAG[A/G]TTCTTAGATGTCAGG | 10580 |
rs529941555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424271 | TTTTATTTTTTCCCC[A/T]TTAAAACAGTTTTAA | 10580 |
rs529947261 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393098 | GTTGTTTCTTCACCA[A/G]TGCTTTTGTGTGGTA | 10580 |
rs529963827 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389689 | GTTAAAGGAGAAAGT[C/T]TGGGAGAACCATAGG | 10580 |
rs529974960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522638 | GGCTGGCACTAACAA[G/T]CGAACAGTAATAATG | 10580 |
rs529990861 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558106 | CCAGCCTGGGCAACA[C/T]CGCAAAACTCTGTCT | 10580 |
rs530004406 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475555 | TCACAGTCTTTAAGG[-/T]TTAGCAAACATGTAT | 10580 |
rs530004899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437102 | GATTTAGGCTCTTGC[C/T]TTAGGGACAGGACTG | 10580 |
rs530005406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409639 | TCATTCAAATTAATG[C/T]AGAGAGGAAGGGGGA | 10580 |
rs530018850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429952 | TATTTGGATTCGATG[A/G]TCTCAATTTACAAAG | 10580 |
rs530021909 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359201 | CCTATGTGGCAGGCA[A/C]CGTGCCTATTGATCA | 10580 |
rs530025253 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414057 | TACTCACTAGGTCAA[C/T]AAGAGAATCAGAGAA | 10580 |
rs530027614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386890 | GCTGGGGCGGGAAGA[C/T]TGCTTGAGGCCAGAA | 10580 |
rs530037717 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448175 | TACACTGGGCCATGA[A/G]GATCCTTCTAGAACA | 10580 |
rs530040871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509498 | AGCAGACTTTAAAAG[C/T]CTTATTGGCAAAATC | 10580 |
rs530083426 | in-del | -/T | 0.253264 | 0.249979 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370253 | TATTCCTTTTGTATC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs530084955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549231 | TGTGGCTAGCATGAC[C/T]GAGAAGCTGAATTTT | 10580 |
rs530090840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556434 | GAGTGCAGTGGTACA[A/T]TCTCGGCTCACTGCA | 10580 |
rs530100972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516643 | TAGAGACTTAACTCT[A/G]AATAATTAAAAGTTA | 10580 |
rs530104176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464750 | TGAGGGACCTCTGAA[A/C]ACACCCAGGTGTGAA | 10580 |
rs530119954 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410168 | ACATTCCAGAAAATT[G/T]TCTACACAATATGTT | 10580 |
rs530122416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319368 | TTTTTATTTACTTGC[A/T]AGTTGGCCTAAGGCA | 10580 |
rs530135636 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373909 | CATTGATTTAGTTAA[C/T]TTGGCAAGTCTTCAC | 10580 |
rs530148574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359726 | GTCAGAAATGGAAAA[C/G]AGGTGGGGACTCTGG | 10580 |
rs530151094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353569 | GTAATGGCGCCATCT[C/T]GGCTCACTGCAACCT | 10580 |
rs530157920 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439358 | AGAGAGAGATTCTGG[A/G]GAGCAGTCTCCTGGG | 10580 |
rs530166897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510118 | ACTGTTTTTAAAAAG[A/G]TAGAAAATAACTCAC | 10580 |
rs530175033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501883 | TCTTCCGCAGAAGCA[C/T]TGCTCTGCCCTTCTA | 10580 |
rs530196886 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406896 | TTGAAGGGTTATTGG[C/T]TTCTCACCATCCTGG | 10580 |
rs530208066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437876 | GTAGCCTAAGCCCCG[C/T]CCAGGTCCCCATCCC | 10580 |
rs530215352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536827 | TCCAAGCAGGGACAC[A/T]TAAGAGGAAAAGGGG | 10580 |
rs530240657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465251 | AAGGCAAAAGAGGCC[A/G]GGCGTGGTGGCTCAT | 10580 |
rs530241942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495463 | CTCTGGGCTCTCCTG[C/T]TACAAGTTCTCAAAG | 10580 |
rs530245505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457784 | CAGAACTTTACAGGC[A/G]ACAGGACAGCAGTGC | 10580 |
rs530269284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431380 | AGCAACCTACCTTTT[C/T]ACTCCAAGTGATTCT | 10580 |
rs530274899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543480 | CCCTTCAGACCAGTA[A/G]TCTCCAAACTTTTTG | 10580 |
rs530289531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530520 | ACTACAGACTCAAAA[C/T]CCTACAAAGTTGTAG | 10580 |
rs530296860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445507 | CCATAAACTCCGTGA[A/C]CTACCCAAGATCTTG | 10580 |
rs530305939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402494 | CTTACCCAGGCTGAA[A/G]TGCAGTGGCATGATC | 10580 |
rs530347004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529819 | AGAATAGATGCCTCA[C/T]ATTATAACCCAAATT | 10580 |
rs530351948 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335980 | CAGGGCCCCAGGAGA[C/T]CTGCATTCTCCTCTC | 10580 |
rs530364444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348101 | CCATCTATACCAAAC[A/G]TACGGGGGCCAAGTG | 10580 |
rs530372491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451142 | GATTCTAACATTCAC[C/T]ATCAGTGACTGCTTT | 10580 |
rs530381838 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557990 | CAGAGGAAGAGGGGG[C/T]TTAACAGATACATAT | 10580 |
rs530389589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425637 | AGATCCACTTTTTCT[C/T]CTCATTCCAAGTCTT | 10580 |
rs530399647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426562 | ATGGAGACATGGCAA[A/G]AAGGCTGAACACAAA | 10580 |
rs530404141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479660 | TGGGGAGAGAGGTCA[A/G]ATGATCCGTGGCGAT | 10580 |
rs530406545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488238 | AATTCACTCAGCTGA[C/T]CAGATTTATAATTAT | 10580 |
rs530413452 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537187 | TCAAAACAGAATTTA[A/G]CTAGTATCATTCATT | 10580 |
rs530420364 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414201 | GGCCTGTGAAAAGCA[C/T]GGCCAGTCAACATAA | 10580 |
rs530431409 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322987 | CACAGAAGAAAATGC[-/A]AATGTAGAGTTAGAA | 10580 |
rs530439351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354336 | TTTCCAGCATTTCTT[A/G]GTGTATCTGCCTTCT | 10580 |
rs530442967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537244 | TGCCTGCTTGTTATG[A/G]CACATGGTGAAAAAG | 10580 |
rs530461245 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400340 | TGGCCTAATGTCCAC[A/C]TGACTCTAGCAGTCC | 10580 |
rs530488561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511017 | CCCTACTTGTCACTA[A/G]CTTTCCTCTCCACCC | 10580 |
rs530500180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333787 | AAAAAAAGAAAGAAA[A/G]AAATTTTTGCTTCTT | 10580 |
rs530532192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448443 | GGGGAAAAAAACTCC[A/G]CAGGGCTCCTATACA | 10580 |
rs530532920 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486834 | CCTGAGATGGTCTAC[A/G]AATATACAAGCACTG | 10580 |
rs530543476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480335 | GGAAAAGCTCCCCGC[A/G]TGGTCAGAACATAGT | 10580 |
rs530549326 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517275 | ATACATCTGAAATTA[C/T]AACAAGACTGACTGC | 10580 |
rs530554529 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389474 | GTACAGTGGTGTGAT[C/T]GTAGCTCACTGCAGC | 10580 |
rs530591755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389010 | ATTGCCTGACTAAAA[C/T]GGGAGGATGGGCAAA | 10580 |
rs530596245 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517780 | GACTCAGGGCTACCC[A/C/G]GAAAAGCACACAACT | 10580 |
rs530620168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473748 | TAGTATAGAATAAAA[C/T]GGTGCTCAGGATTTC | 10580 |
rs530630531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431879 | TGCTCCTAGTTTACA[A/C]TGGGCCTTTGAGCTA | 10580 |
rs530650337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557899 | CCTACTTTCTCGTCT[A/G]TTTCTCCAATCTCTC | 10580 |
rs530659113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381859 | CATTAGCTTCCGACA[C/T]GGTCTGACTTTGGAT | 10580 |
rs530674823 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439212 | ACTTACTCATACCCC[C/G/T]CCTTCATGTAGGTGA | 10580 |
rs530704079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418894 | GAGACTCTGTCTCTA[C/T]AAAAAATTTAAAAAA | 10580 |
rs530710416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360975 | TGCGCCACCACACCC[A/G]GCTAATTTTTGTACT | 10580 |
rs530732631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360480 | GTAGCTGAGTCTCAG[A/C]CAATCACAGCAGCCA | 10580 |
rs530747511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320759 | AAAAACACCTCCCCT[G/T]ACTCTGCTATTCCCT | 10580 |
rs530747928 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312148 | AATAGAATACTTATC[A/G]TAAATTTTAACACTT | 10580 |
rs530769059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466395 | GCAGTGAGCCAAGAT[C/G]ACGCCACTGTACTCC | 10580 |
rs530804415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496603 | CAAAGCTCATAAAGT[A/G]TAACAAAATTAGTTG | 10580 |
rs530825995 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489307 | TCAAAAAGAGCCCCG[C/T]CAGCCCTTCACCTTG | 10580 |
rs530860707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460109 | AAAGACAAGCAAAAC[A/G]GAGGGGATGAAAAGG | 10580 |
rs530863614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446269 | AGAGTTGTTAAGAAA[C/G]CATCCAGATAATTAA | 10580 |
rs530865569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453582 | ACCTCAGGTGATCCA[C/T]CCGCCTCGGCCTCCC | 10580 |
rs530867305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504473 | GTTACATGTGCAGAC[A/G]TCTGTCTTCAAGTGA | 10580 |
rs530870019 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421019 | TTAAGAGAAAGGACT[A/G]GGCTAGGTGTGGTGT | 10580 |
rs530875539 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413247 | TGAGATTCCTAGGCT[C/G]TTCTCCAGACCCACT | 10580 |
rs530887157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489784 | GAGTCTAGACAGCCA[A/G]CCTCCTGTGGCTGAT | 10580 |
rs530894906 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405521 | CCACCATTAAATCCA[A/G]ATCTCTAGGGGGATG | 10580 |
rs530925440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446615 | GGTGTTTTGCCTCCA[C/T]AGCTCCCCCATCCCC | 10580 |
rs530944403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497280 | ATGGCATGAAGCGTG[C/G]GCAGGACTTCATCAT | 10580 |
rs530952698 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444780 | TCTTGTGAACCAAAC[A/C]AAAAGGATACCTCAA | 10580 |
rs530955243 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390524 | CAAAACTGCATCTGG[A/C]CAATTTTCTTCATCT | 10580 |
rs530970517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475198 | AGCAGATCTGGCACA[C/T]GGTGGTGGGGGTGGT | 10580 |
rs530972371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467423 | CAAAGACAGCAACTG[C/T]GTTCCTATCTGGGGC | 10580 |
rs530985031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533056 | CCTCCCTATGGTACC[A/G]TATATAAACCCTGGG | 10580 |
rs530999107 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370143 | CACTGGGGCTGGAGA[A/T]CTGTCTTGGTTCTGC | 10580 |
rs531002010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518475 | GTCATTTCACCTCCC[C/T]GGGCCCCAGGGAGGC | 10580 |
rs531003827 | snp | C/T | 1.77836e-05 | 0.00298186 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377356 | TTACAACACAGTTAA[C/T]ATCCCCTTTGCAGCT | 10580 |
rs531004539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368708 | TGCTGAAACCTGTTG[C/G]GCTTGTATGCTTTCA | 10580 |
rs531020255 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493957 | ACCTCTTCAAGGACA[C/T]GAATTCAGCATCCTC | 10580 |
rs531050348 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532336 | GCTGGGAACCTTCCC[A/G]GCCTCTGGTTCCTGC | 10580 |
rs531075050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397492 | ATATTTGGCTGAAAG[A/G]ATACAGATTTTGAAA | 10580 |
rs531091284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428139 | CATTTAGCTGGGTGT[A/G]GTGGCTCATGCCTGT | 10580 |
rs531099722 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324418 | GGAAATGTCCTCAAC[C/T]GTTAGCAAGCCCTGC | 10580 |
rs531112232 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433501 | CTGAGCTATGCAGAA[C/G/T]GCCACAGTTTTGTTT | 10580 |
rs531124940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525655 | TAAAAAGCTGCCTCA[C/T]TTCTTTCTGTGGCTG | 10580 |
rs531137496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384183 | GGGCAATTATCTTCC[C/T]TCATCCACCACTTTC | 10580 |
rs531159108 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323317 | TTTTGAAAACTTCCT[C/T]GGTAATATATGAAGT | 10580 |
rs531160849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414174 | CTCAGCTCACCACAC[A/G]ACCCCCGACCTGGCC | 10580 |
rs531164314 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351667 | CTCAGCCCAAAGCCT[C/G]TTGCTTCTGGCAGCA | 10580 |
rs531185597 | in-del | -/AAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494096 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GGAATGCCAGCAGCC | 10580 |
rs531202263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513302 | TTCAGAGCATTGAGA[C/T]ACCTTTCGATCCAGC | 10580 |
rs531215037 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320511 | CAGCCTCCCAAGTAG[A/C]TGGGACTACAGGCGC | 10580 |
rs531217262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335875 | TACCTTTGTCCAAAT[C/G]CTCTCTGGGTCTTTG | 10580 |
rs531220482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354482 | GAACAATGCTTTGTG[C/T]CAACAGAGGGGTGGG | 10580 |
rs531221873 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473426 | CCTGAGGTCAGGAGT[C/T]CAAGACCAGCCTGAC | 10580 |
rs531229300 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398443 | TGCAGGACTGGCAGG[C/G]CTGTGCTGCCGGGGA | 10580 |
rs531232054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559214 | TGGCCCTGCCCTTTC[A/G]TTGTTTACAAAGAAA | 10580 |
rs531264730 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519301 | CCACCAGCACCTGTG[A/G]ATGTCACCACCTCCT | 10580 |
rs531304312 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553180 | ATCGCACCTCTGCAC[G/T]CTAGCCTGGTGGACA | 10580 |
rs531324359 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362645 | ACAGCTCACATTAAT[A/C]CCTTTACTCTCCACC | 10580 |
rs531332416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356601 | AGATCCCGCACACTC[A/G]AGGAGGAGGAGATGG | 10580 |
rs531348349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507119 | GCCCACCTCAGCCTC[C/T]CAAAGAACTGGGATT | 10580 |
rs531352421 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475858 | AATTTCACAAATGAA[A/G]AAAATGAGGCTCAGA | 10580 |
rs531367897 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371089 | AATCAGCAGCCTCTC[C/T]GCATATATTTGAAGA | 10580 |
rs531369699 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552734 | CCACAGACCCTCTCT[C/G]AGAAACTTGTGGAAG | 10580 |
rs531393251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541004 | CTCCTCATCCAAGCT[C/G]GTCAGCCAGAGGCCC | 10580 |
rs531412461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393550 | GCCTTCATCATCGCT[A/G]TTTTCCAGGTATTGC | 10580 |
rs531425618 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413202 | GGTGTGGACCCCAGC[A/T]TCTGAAACCCCTGAG | 10580 |
rs531429288 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322633 | GCCACAGAATTCTTA[G/T]AAATAATATTTCTGT | 10580 |
rs531440436 | snp | A/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442172 | ATAGTACAGGTAATC[A/C]TTTGTGTCTGGCTTC | 10580 |
rs531462029 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562685 | ACTGCACAGACTGAT[C/G/T]GGAAACTCATCAGCA | 10580 |
rs531462085 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530265 | CACCAGACACAACCA[A/G]GTGTTCCTTCCTACC | 10580 |
rs531463061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527253 | ACATGGGGAAACCTC[A/G]TCCTTACTAAAAAAA | 10580 |
rs531483574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483859 | TTTAAAGAAAAAAAT[A/G]TTTGTTTCACCCTAC | 10580 |
rs531510897 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442135 | TGTTTTACCTTTTCC[A/G]GGATTTTATATAAAT | 10580 |
rs531512542 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434633 | ATACCTGTAGGGAGA[A/G]CTAGGCCTGAGGCGT | 10580 |
rs531520735 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534060 | GTAAACCAAGACCAG[A/C]GAGGGGGTGGGACTT | 10580 |
rs531526096 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510612 | TTGCTTCTTACAGTA[C/T]CATCAGTCAGTATCA | 10580 |
rs531528735 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373608 | CCCAGTTGGTGTGAG[-/A]AAAAAAAAAAGTAGA | 10580 |
rs531549722 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522738 | TATCTGGTTCAATCA[A/G]TCCTTACAACTGAGG | 10580 |
rs531550190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535687 | AATGAAAGAGGGTGT[A/G]ATTGATCATTCACTG | 10580 |
rs531564291 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547996 | TGCAGCCCGCTGCTC[C/T]ACAGGGGTGATGGTA | 10580 |
rs531577390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330506 | ACTTTCCTTTTTTTT[G/T]GTTTACTTTTTAAAA | 10580 |
rs531582991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337493 | GATGGGTGAGTGTGC[A/G]TTTGAGCATGTGCGA | 10580 |
rs531610279 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507615 | ACAAAACGGGACACA[G/T]AGAAATTAAAGGGCA | 10580 |
rs531625359 | snp | A/G | 0.000167895 | 0.00916075 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414834 | ACAACTATTACCTCC[A/G]GCTGGGCTGCACTGG | 10580 |
rs531625474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423070 | TTGTTAATAAGAACA[C/T]TTATGCATGCAAAAT | 10580 |
rs531653007 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441296 | AAAACAGAGCTGAAC[C/T]AGGAGTCACCTGGCC | 10580 |
rs531676206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515442 | GCAGTCACCATTTCT[C/T]GGGGTGACTTTAATG | 10580 |
rs531701285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469974 | CTACAAGGCACCTGT[C/G]GAGAACCACTGAACT | 10580 |
rs531704130 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561487 | CATGCCTCTGGAACC[A/G]TCCACTCTGGCAGCG | 10580 |
rs531731093 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404089 | AGGCCTTTTTTATCT[A/G]TTCTACCCTTCTTTC | 10580 |
rs531733863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371156 | CCAAGCAAAAATGAA[C/T]TGGGTAGGTGTGGGG | 10580 |
rs531740287 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380209 | CCTGGTAAACTATTG[C/T]GGTATCAATGAGAAA | 10580 |
rs531754081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505472 | ACAGAAGAGCTCTAA[C/T]TGCAGAGCCTCAGCC | 10580 |
rs531774296 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449870 | TTACATTGTCTAACA[G/T]ATTAAAATGCATGGC | 10580 |
rs531774307 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451043 | AAGAAAAAATTCTAG[C/G]AGACAAGCTAAAAAT | 10580 |
rs531778046 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326059 | GACCTTGTGAAGTTT[A/G]TACAAGGTAGTGTGA | 10580 |
rs531793597 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358704 | CGCACATGCACAGAC[A/G]TGCGCGCGCGCGCGC | 10580 |
rs531794035 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507901 | GGTGACAGAGCGAGA[C/T]TCTATCAAAAAAAAA | 10580 |
rs531800808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378459 | CCATATTATCACATT[C/T]GACCCACCCCATCTT | 10580 |
rs531820898 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338071 | TCAGGGTCAACCTGG[C/G]CCCCCAGGTCCTACT | 10580 |
rs531831809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400921 | TTAGGCAAGAGAGAA[A/G]TCACAGGAACACTCT | 10580 |
rs531832811 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356326 | CATCCATCTCCTTGG[C/G]ATGGAGCTTGGTTGA | 10580 |
rs531839534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555135 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10580 |
rs531860974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514966 | CCACTCCCCTCCCAC[A/C]CTACAGCTTCATCTC | 10580 |
rs531873342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464111 | GTGGGAGGATCACTA[A/G]AGGTCAAGACAAGCC | 10580 |
rs531874755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415687 | GTGGTTTTCCTGTGC[C/T]GGCTGTGCGGGAGAC | 10580 |
rs531892530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549184 | ATGCCGACCGTAGGG[C/T]AGTCACTAGCCACAC | 10580 |
rs531918179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317450 | TGTTTGTTGAGAGAA[C/T]GTCAATAAAAGCATA | 10580 |
rs531935234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457068 | TAGAACTCAAAGACG[C/T]TTATTATAACTAAAT | 10580 |
rs531936439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339063 | CCAGAGAGGCTGTGT[A/G]CCATCAGCACTGTTG | 10580 |
rs531938731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346506 | CATGGACAACAAGGA[C/T]ACATTTTCACAAATT | 10580 |
rs531959861 | in-del | -/GAG | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552981 | GCACTTTGAGAAGTT[-/GAG]GAGGGAGGATTGTTT | 10580 |
rs531963701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486182 | CAGAGAGGTGGCAAC[C/T]TATACAAATTCTATT | 10580 |
rs531991528 | in-del | -/AAGTATAAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496598 | GACACAAAGCTCATA[-/AAGTATAAC]AAGTATAACAAAATT | 10580 |
rs532000749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371893 | GTGATTTAAGAAAAC[A/G]AACAAACAAACAAAC | 10580 |
rs532023607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501580 | CTTGCTGAAGCCAGG[A/C]ATGGTGGTGTGGGTC | 10580 |
rs532023635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493854 | TATGGTTTAGAGGTC[C/G]AAGCACTGTCCAGAA | 10580 |
rs532025012 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339667 | CAAAGATTTTGGGGG[G/T]TTTCACTTTTTCTTT | 10580 |
rs532044170 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435720 | CTGCAAAGTCAGCAT[C/T]GTGCTGGTGAGCCTG | 10580 |
rs532052322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430550 | TACGTCAATGCCACA[C/T]TGTAACCACTAGAGG | 10580 |
rs532063411 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364604 | ACAGACGTGCACCAC[C/T]AAGCCCAGCTAATTT | 10580 |
rs532082194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500842 | AATCTCTGATGTTCA[G/T]TTTCCTCCCCTGTAC | 10580 |
rs532092539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443930 | TCGAGAAACACACAA[C/T]CTGCTGTTATCTGTA | 10580 |
rs532094604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345867 | GAACTCTCTTTTTGA[A/G]AAAAATTTTACAGGG | 10580 |
rs532097340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478557 | AAAAGAAAGTGATGA[C/G]TCTATTTTGGTGTCA | 10580 |
rs532106978 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541464 | CTGCAGAGGGCCCCA[A/G]CCTCCCAAGCCTACT | 10580 |
rs532123561 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498928 | AATGATATCTGAATA[A/T]GACTGTAGCATTGTC | 10580 |
rs532142820 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522227 | GCCTCCTTTTCTCCC[C/T]TTCCTTCTCCTTGTT | 10580 |
rs532157447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386960 | CTACAAAAAAATTTT[A/T]AAAAAATTAGCCATG | 10580 |
rs532172963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465324 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10580 |
rs532180405 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325332 | ACCTAGCCTCCTTCC[A/T]CTCAACTTCATTCAT | 10580 |
rs532195544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529519 | TAAGATGTTTAAGAA[C/T]CACCTGGAGTGCTTG | 10580 |
rs532203364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471482 | CAGCACTTTGGGAGG[C/T]CCAGGTGGGAGGATT | 10580 |
rs532205599 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95420604 | TCAAAAAGCCAGGCT[C/T]ATTCGCAGCTCCTGG | 10580 |
rs532219292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401436 | TCAGTGAGAATGAGG[C/T]CCATGAGGTAAGGAT | 10580 |
rs532227673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323267 | AAGTCTGCTGTATTT[C/T]AGAAACTTATAAAAA | 10580 |
rs532243627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436607 | TTGTTTGGAATTATT[C/G]TTTGAGATGCATCTT | 10580 |
rs532253824 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353439 | TTTCTTTCCATGGAC[A/C]GGTGCAAGTTTCTTA | 10580 |
rs532274985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380597 | CTGTGCTCCTCTCTG[A/G]ACTTTCTGCTTGAAA | 10580 |
rs532288927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332255 | CCCTGCCTGGCATTT[C/T]TTTTTCCTGAAGTCT | 10580 |
rs532298377 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456748 | AAAAAAAAAGAAATA[C/T]GCCTCAACCATATAT | 10580 |
rs532304276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332968 | GTCAGGAAAGGTGTT[A/G]AAGGAAATCAGAATA | 10580 |
rs532306947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560119 | GGAGAGATGGAGTCA[A/G]AGGCCTGACACGCCA | 10580 |
rs532315179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416575 | AAAGCCCCCAACTCC[A/C]TCTCAAACCTCCTTC | 10580 |
rs532324318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516273 | GAGGGACCCAGCAAT[A/C]TGTGTCTTAACAAGC | 10580 |
rs532336735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372862 | GGTTACAGGTGACTT[C/G]TAACTCTGGATCCTC | 10580 |
rs532346038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325952 | CCTCGGACTCTGACA[A/G]GGGTAAAGGAAGAGA | 10580 |
rs532346734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523390 | CTGCAGCAGACTGCA[A/G]CCAAGCTCTGCAGCC | 10580 |
rs532360223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402800 | TTTTTTTTATAGAGA[C/T]GGGGTTTCACCATGT | 10580 |
rs532404622 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502752 | TATTAATGCACAGGA[A/C]AGTATCTTCAAAATC | 10580 |
rs532428962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347523 | CACTGTAACCTCTGC[C/T]TCCCAGGTTCAAGCA | 10580 |
rs532438322 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474220 | AGATCATAAGAAATC[C/T]TTAAAAAAAATAAAC | 10580 |
rs532445778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495989 | GAGTGCAATGGCATG[A/G]TCTTGGCTCAGAGCA | 10580 |
rs532446373 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562483 | TGGCCCAAGGTCGCA[A/G]AGCCAGCAAGTACTG | 10580 |
rs532474366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516687 | ATTTCTCTTCCCCAC[A/G]CTCCACAGGTATACT | 10580 |
rs532489318 | in-del | -/T | 0.306182 | 0.243605 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367213 | ATACCCAGCTTTTCC[-/T]TTTTTTTTTTTTGGG | 10580 |
rs532490278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359753 | CTGGTAGAATACCGC[A/G]ACATCTCCACCTTAG | 10580 |
rs532495109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410285 | AGAGGTATTATTGTA[C/T]CTAGATTTTCGAAGT | 10580 |
rs532507533 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411070 | GGTCAATCTGGTTAC[C/T]GAAAAACCAAATTCA | 10580 |
rs532515728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550481 | GTCTCCCTCCCAGTG[C/T]GTCTTATCCTCCACT | 10580 |
rs532532197 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428287 | TGTGGTGGCAGACAC[C/G]TATAGTCCCAGCTAC | 10580 |
rs532540248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510909 | TGGTTCCACCTCAAA[C/T]TGTGCTGTTTTCTAA | 10580 |
rs532552544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480423 | CAGGCACTAAGCAGA[C/T]GCAGAGGGCTGCTGT | 10580 |
rs532567600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557184 | CTCCAGACCTTGAAC[C/T]ATTATCACCTTTTAT | 10580 |
rs532568945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431943 | GCCAATCCCAGGCCT[A/G]AGCCCTCCCCACCTC | 10580 |
rs532572482 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95311874 | TGCAATGAAGAAAAA[C/T]AAATGAACAGAAAAA | 10580 |
rs532572819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530619 | TTCTCTCCAGAGCCA[C/T]CATGATCAGAGAGTT | 10580 |
rs532575146 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390240 | GGGAAAAAAGCTGGT[A/C/T]TCTGGGGCTTCACCT | 10580 |
rs532580565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549967 | TGCAGCTAGGCCCTC[A/T]ACAAGCTAGGCTTGT | 10580 |
rs532598893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445611 | GCAGAAGATGGGAGG[A/G]AGAAGTCCCCAAGGT | 10580 |
rs532620217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403852 | GGCATGAACCACTGC[A/G]TCCGGCCCACCCTCA | 10580 |
rs532635395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537490 | CTAAACCTATCACAC[A/G]CCCCTGGGTAGAGCG | 10580 |
rs532646736 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378547 | ATGACAGGGGGGCAG[G/T]CCCACTAAGTTTGCG | 10580 |
rs532663418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459435 | ACCAGTGGATAGGGA[C/T]AGAAAATCCCAGCGA | 10580 |
rs532677918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503351 | TGCTGCAGACAGAAC[C/T]CCAGCACAGCCATTA | 10580 |
rs532685316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473352 | ATATTGTAGATCACC[A/G]GGCACGGTGGCTCAC | 10580 |
rs532690785 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311457 | AATCTAGACCCATTA[A/T]ACATATTTTATAATG | 10580 |
rs532712284 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389167 | CTCAACCTAAATCCT[C/T]CTCTGGCTTTACCCC | 10580 |
rs532717216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538012 | AGTGACTTGGGAGGC[C/T]GAAGTAGGAGGATCA | 10580 |
rs532770477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418218 | GAGTAGCCGAGACTA[C/T]AGGCCTGTGCCACCA | 10580 |
rs532784246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411898 | AGCTCCCAACACACA[A/G]TAGGAACTTCACAAC | 10580 |
rs532794196 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419835 | TTTCAGAAGGTGGGT[C/G]AGTGAAAATATGAGG | 10580 |
rs532796599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334043 | TGGTCAGATTCTCAA[A/C]CTACCTCCCCAATAC | 10580 |
rs532796642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341995 | GCTCAGAAAATTTAT[A/G]CAACACAGAGCAATG | 10580 |
rs532822726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396160 | GGGGTCATGTCCTGC[C/T]CAAGCACTGGCCTGC | 10580 |
rs532838565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382576 | TTATTGAAGGGTCTG[C/T]CTTTCTCCCAATGTA | 10580 |
rs532852498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504570 | AAAGACTCCACCACT[G/T]TTTATACGTGTATCC | 10580 |
rs532854365 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352606 | AAGCCCAGTGCCATA[A/G]AAAGAGTGCTGGTCC | 10580 |
rs532860094 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362702 | ACTGTACAACAAACA[C/G/T]GCATTGCTCCCCCAG | 10580 |
rs532864063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438717 | GGGCAGCCTCTGAGC[G/T]ACCAGCAGGCCCAGC | 10580 |
rs532878022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398453 | GCAGGCCTGTGCTGC[C/T]GGGGAGAGCTGGGTC | 10580 |
rs532879956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551097 | CCCTCTTGCAGTCTG[A/C]TCAGCCTGGTGATTT | 10580 |
rs532889470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518388 | CTTGGAGACTCAATG[A/C]AACATGATATAAAAC | 10580 |
rs532972018 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358134 | GGATAGGGGAGAACA[C/G]GGGGAGGATCACACA | 10580 |
rs532972127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473849 | TACTAATTTTTAAAT[G/T]TTGCACATGGTCAAT | 10580 |
rs533007905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512278 | CAAAAATTAGCCAGG[C/T]ATGGTGGCGCATACA | 10580 |
rs533028235 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447140 | AACAAGCCTCTGTCT[C/G]AAAAACAAAAACAAA | 10580 |
rs533038005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334703 | AATTGGGCCGGGATG[A/G]TGACTCAACACTGAC | 10580 |
rs533038617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453152 | TTAGCCGGGTGTTGT[A/G]GTGCATGCCTGTAGT | 10580 |
rs533039304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558431 | AAACCTCCCAACCCC[C/T]CAAATTCCTCAGTTT | 10580 |
rs533055988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529889 | AGCTAGGTCCTTAAA[C/T]AGAGCCTCTTCCCAA | 10580 |
rs533060551 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330743 | CTTAAACTCCTGGCT[C/T]CAAGTGATCTGCCCG | 10580 |
rs533105885 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405561 | TCTGAGTTTCGACAA[C/G]CTCTCCAGGAATTTC | 10580 |
rs533125859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433534 | TTTTCAAATTGCTCA[C/T]AGCCTAGATCCCTGA | 10580 |
rs533131411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343533 | TGAGGTGATCCGCCC[A/G]CCTCGGACTCCCAAA | 10580 |
rs533136457 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446779 | AAGATAATCAAGAGC[C/G]TCCTTAACTCCACCA | 10580 |
rs533153791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505309 | GGGCTTATTCCCATA[C/T]GTGGATGCTGGAGTT | 10580 |
rs533161744 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486722 | CTAGATCATTTATAA[A/G]GAATAAAAGGGATAC | 10580 |
rs533172476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397577 | ACTTTTAGATAGAAT[C/T]TCTCCATATATAGAC | 10580 |
rs533173501 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505154 | TTTGAGTTGGATTGC[C/T]TCCTTGTATGGTTAC | 10580 |
rs533180860 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512391 | ACCACTGCTCTCCAG[A/C]CTGGGCAACCAACCG | 10580 |
rs533197181 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336695 | CAGGCACCTGACCAC[A/G]TCTGAAGGCTTCAAG | 10580 |
rs533200679 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320432 | GTCTCTAGGCTGGAG[C/T]GCAATGGCGCAGTCT | 10580 |
rs533222612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526278 | AATCCCCTGTCCCTC[C/T]GGGCTGGGCCCTGTG | 10580 |
rs533223216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460644 | TTGAGCCCAGGACGT[C/T]GAGGCTGCAGTGAGC | 10580 |
rs533223294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361168 | ACTTTGTTCTGTCAT[C/G]ACTCTTGACCATAAC | 10580 |
rs533241209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497956 | AAACTACCTTGTTTT[C/T]TCGGTGACAATTCCC | 10580 |
rs533250320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398064 | CCTGAGTCCCCATTT[C/T]CTCATCTATAAGATG | 10580 |
rs533275243 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392546 | TTTTCCTTTTTATTC[-/T]TTAAGACTATTTCTT | 10580 |
rs533279701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453777 | TTTGTAGGATGTGGA[A/T]GCTGCGTATGTGGAT | 10580 |
rs533282197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350681 | CTTCACACAATTCAT[C/T]CACCTACATGTGAGC | 10580 |
rs533284094 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95336288 | AAGTAGAGATAACTT[A/C]CAAATGACCTCAAGT | 10580 |
rs533316780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468832 | GCCGGACAGGGCAGA[A/G]TGGAGTTCTGCCTCC | 10580 |
rs533316860 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382250 | ACTAGGTGATCTTAG[A/G]CAAGTATTTCACCTC | 10580 |
rs533320674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421440 | GGGGGATTTCTTTTG[C/T]AGGATACAGCTGGGC | 10580 |
rs533345422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462282 | GCAGCCATTCAAGTA[C/T]CAAACTTTTTGTAAG | 10580 |
rs533389984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429282 | TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 10580 |
rs533390252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475853 | ATCTCAATTTCACAA[A/G]TGAAGAAAATGAGGC | 10580 |
rs533392551 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409142 | AGCAGCTGACATTAC[A/C]CTTGGCATTTCCCAA | 10580 |
rs533394971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428183 | TGGGAGGCCAAGGCG[G/T]GTGGATCATGAGGTC | 10580 |
rs533422685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328885 | CTAGCTGCTTTCATC[C/T]CTATTATATTTCATT | 10580 |
rs533425940 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519339 | CCCTCCAGCACACAG[A/G]CCAGTGCTGCCACCA | 10580 |
rs533448168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391266 | ATGAAGAGTTACTTC[A/G]TGGGGCTGCTGGGAG | 10580 |
rs533471271 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457271 | TATGTATTCTATTCC[A/C]ATCAGTGTAGGATGT | 10580 |
rs533478048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461592 | AATACAACCAAGTGA[C/G]GGCAACACCAAGTAT | 10580 |
rs533490901 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549069 | CTCCACCATGAAATG[C/T]TAATCATAAATGTCG | 10580 |
rs533498404 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463170 | TGTGCTCAACAAATA[C/T]GCCAAGTGCTCATGG | 10580 |
rs533516563 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502528 | TCACTCACCTTCCAG[A/G]GTGTGCTTCTCACAT | 10580 |
rs533518290 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559869 | AGGCTGTAGATATGT[C/T]CATCATCTGTCTTCT | 10580 |
rs533522377 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551587 | CAGTCAAGGATCAGC[A/G]TGCATGGAAGGATAG | 10580 |
rs533524917 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479422 | AAAAAAAAAAAAAAA[-/A]GGTGAGGGGAATATA | 10580 |
rs533534106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322657 | TTTCTGTGGGTTAAC[C/T]AGGCATCACTCTAGT | 10580 |
rs533541809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343928 | TGTCTCTGTGAGAAG[G/T]AATGTCTCGGGCCAC | 10580 |
rs533548274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384553 | CAAGAAATGCATGGG[G/T]ACAAACAGCCAAGGG | 10580 |
rs533561533 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425933 | TAGAGCTCCCAAGCT[C/G]GGGGGAGTGCCTCGG | 10580 |
rs533564826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519894 | ACACCAAAAACACAA[C/T]AAAACCTGACAAAAT | 10580 |
rs533571355 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451471 | AGTTAACCAAGACAA[A/G]TCTTAAATGCAAAAA | 10580 |
rs533596328 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428850 | GCCATCTGACATTAG[A/C]TATCTGCAAAGGCAT | 10580 |
rs533598317 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399315 | TAGTTCTGTTTAGAG[C/G]AGGGGTCAGCAAACT | 10580 |
rs533606735 | snp | A/G | 0.000125086 | 0.00790742 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356723 | CCTCCTGCCGCTGGT[A/G]CTGTACTCCTGGAGG | 10580 |
rs533609200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447386 | GGTGGGAGGGTCACT[G/T]GGACCCAGGAGGCCT | 10580 |
rs533614043 | in-del | -/A | 0.455977 | 0.141681 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432346 | ACACCCCCCCCCCCC[-/A]AGAGGTATCTGATGA | 10580 |
rs533653147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350937 | GGAGGGCTGGACTCA[G/T]GAAGGCAGCCAATGG | 10580 |
rs533662548 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553371 | GAAAGAAAATATTAT[A/G]GTATACTATATGGCT | 10580 |
rs533665928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553301 | TTAGCAATAAGTACA[C/T]AGAAACTAAGTAAAT | 10580 |
rs533686535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483264 | AGGAAAAAAACCTAA[A/G]AAACATTCAACTCCT | 10580 |
rs533700305 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322307 | GGTTAAAAAAATAGA[A/T]ATTCCAGTAGTGGAG | 10580 |
rs533721233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421843 | CCAGAGTTGTCCAAA[A/G]GCTTGAAACCTATTC | 10580 |
rs533737080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370508 | TCGGCCTCCCAAATT[G/T]CTGGGATTACAGGCG | 10580 |
rs533750872 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472478 | AACAACTGTGGTATG[A/G]CTTCTGAAAGCTACT | 10580 |
rs533767285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476103 | GGAGCTAAAAGGTTT[C/T]CACATCATCTCCAGG | 10580 |
rs533771858 | snp | C/T | 1.83357e-05 | 0.00302779 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414548 | TCTGCGGAGGTCCTC[C/T]GGGGCAGGAGGGACC | 10580 |
rs533783321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519569 | CGTCAAAATAAAACC[C/T]GAATTTTAAGCAAGA | 10580 |
rs533823015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434770 | AACATTTGGGAAACA[C/T]TCAGGCAGTTGAGGA | 10580 |
rs533829637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440414 | ATCATCTTCCCACCC[C/G]ACAGCCTGCCCCACC | 10580 |
rs533847491 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350412 | TACAGCATTTGGCTA[G/T]CATGAGAATTTCGAC | 10580 |
rs533855956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429062 | AGTCCGGAGGGTGAC[A/G]TGGACACTGTCAGAG | 10580 |
rs533856791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514359 | TCCTGATGCTGGTTT[A/G]TTTCTGGCTAAAACC | 10580 |
rs533859143 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323815 | CAACAAAGCAAAACC[C/T]CATCTCTACAAAAAA | 10580 |
rs533862261 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517763 | ACAAATTGGCGGTCT[C/G]TGACTCAGGGCTACC | 10580 |
rs533863090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378561 | GGCCCACTAAGTTTG[C/T]GATGACACCAAGCTA | 10580 |
rs533884883 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445917 | CACTTAATATTTATT[G/T]AAAAACTAAGCTGTA | 10580 |
rs533888420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408003 | AGTTTTGAGGTGTGA[A/G]ATAGCCTTTCTTTCA | 10580 |
rs533894409 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547933 | CCTCCAAGAAAATAC[C/G]AGGGCCCAGCTGGGC | 10580 |
rs533895138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441057 | AGTGGGGCCTTCAGG[A/G]TGCGTGGGAAATCTG | 10580 |
rs533896481 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477331 | CCCACCCAGCCCTGC[A/C]CTGGGTGGGAGTCCT | 10580 |
rs533905870 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505940 | TTTTTTACAAATCAT[C/T]TTCTCTAATATAAAA | 10580 |
rs533935402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449291 | ATCCAGGCTGGAGTG[C/T]AGTGGCACAATCTCG | 10580 |
rs533939251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508026 | GAGTCACACCCTGTC[A/G]CCCAGGCTGGAGTGC | 10580 |
rs533940734 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497500 | GAAAAATTCAGACAT[C/T]CATAGCCGTGTCTGA | 10580 |
rs533955202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554569 | CTAGGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 10580 |
rs533956650 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400182 | AAACTCTTCATTTAC[G/T]TTCTCTCATTTTATC | 10580 |
rs533987477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363552 | GAAGGTTAATCAATG[C/T]TGAAATACATTGAAA | 10580 |
rs534010864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468494 | TGGTTCCCACTTCCT[C/T]CAGAAAGATTTTCTA | 10580 |
rs534021319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541400 | ACCTCCAGCTCCTCC[C/T]TTGCCTTATTTCTCT | 10580 |
rs534025070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414964 | GAGGTACTCTGAGAA[A/G]TATTTAATCAGTGCC | 10580 |
rs534070071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500374 | GATCTAGAAAACTCT[A/G]ACCCCTGGCTACCTG | 10580 |
rs534073948 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483778 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 10580 |
rs534094087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337511 | TGAGCATGTGCGAGC[A/G]TGATCCTGATGTGTG | 10580 |
rs534100705 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523943 | TCCAACTTTTCTTTT[A/G]ACAACATATAATTTC | 10580 |
rs534103720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421043 | GTGGTGTCTCACACC[C/T]ATAATCCCAACACTT | 10580 |
rs534138396 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474139 | AGTGGACAGATAGCA[A/G]GAAAGAACTCCCTGT | 10580 |
rs534151291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330962 | CAAAAACTAAAAGGC[A/G]AAACTTCTATTTTTC | 10580 |
rs534153471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535123 | GATACAGATGCCCAG[A/G]AATTCTGGCCAGCAA | 10580 |
rs534185688 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442589 | CCTTCCACCATGATG[A/G]GAAGCTTCCTGAGGC | 10580 |
rs534186483 | in-del | -/CTCT | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423701 | ACATTTACTGAACAC[-/CTCT]CTAAGTGCCACTGTG | 10580 |
rs534192323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499400 | TAAATTACAATAACA[C/T]TTATAAAGCCAAACA | 10580 |
rs534210254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477722 | CAAAGGACAGCAGCA[C/T]TTATGGTCAGAGGAA | 10580 |
rs534213393 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462387 | CTACAAAAGAAATAT[A/G]AGCACACAACTAAAC | 10580 |
rs534229636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528434 | CTTGTCCAAAATCCA[C/T]TTCACTCACACCTGA | 10580 |
rs534247057 | in-del | -/TTTTTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390650 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAGACAGAGACTCAC | 10580 |
rs534253462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455753 | CAGCCTAAGCAACAC[A/G]TTGAAACCCCATCTC | 10580 |
rs534274576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324706 | TGGATTAAGGTGTCC[A/G]TATCACAAAGGAAAG | 10580 |
rs534296987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95416112 | AGGGAATCCTTATAG[C/G]TATTGTGGATGGTGG | 10580 |
rs534300714 | snp | C/G/T | 0.000151913 | 0.00871419 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357612 | GACAGAGGCCTGCAG[C/G/T]CTTCACCCAGTTAAT | 10580 |
rs534313383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365020 | ATGTTCAGAGGATTA[A/G]ATGAGGTAAGGTAGA | 10580 |
rs534321057 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453924 | TATATATGAAACACT[A/G]TAAATTGTTGTGTTA | 10580 |
rs534322019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457391 | GTGCTCAGGCAGTGA[C/T]GCTACCACTGTACAG | 10580 |
rs534323367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464900 | TCACTGTATAGAAGA[C/G]GAAGCAGTCCAGGTG | 10580 |
rs534329900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448455 | TCCGCAGGGCTCCTA[C/T]ACACTCAGAGGGGTT | 10580 |
rs534338421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364179 | ACCAAGCCCGATTAC[C/T]GAAAAATCCCCAAAT | 10580 |
rs534338891 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561965 | TAATGCTTCCCGGAT[A/G]TTTCCTCATTTGATC | 10580 |
rs534343732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471031 | AAGACTCTGTCTTGG[A/G]AAAAAAAAAAAATCT | 10580 |
rs534358851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325413 | AAGAGGATCAGTGAA[C/T]CAAATATAGTAAGAA | 10580 |
rs534365593 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522174 | AGACAGGAAGGGTGC[A/T]GAAGTTCTGACAGGG | 10580 |
rs534392575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379462 | AGTTTGTAAGTCTTC[C/T]GTAGGGGGTTTTGAA | 10580 |
rs534406772 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334735 | ATAAGGATGTCCCCG[A/G]GTGCCTTGGGTTGAC | 10580 |
rs534416631 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532157 | GTCCCAACCCCCACA[A/G]CCTACAAGGCCTGTT | 10580 |
rs534426614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331842 | AGTAATTAGACTTCC[A/C]TATCATTTAAAGCAG | 10580 |
rs534444691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372342 | AAGAAAAGACGGGGG[A/G]GAAAAAAGAAAAAAA | 10580 |
rs534453440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464568 | CTCAGGGTGCTCGCT[A/G]TCTAGCCCACTCTTT | 10580 |
rs534497594 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458032 | AAAAAAGAAAAAAAA[A/G]CATTTCAGGGCTGGA | 10580 |
rs534508466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353804 | AGCCACTGCACCTGG[C/T]CACGGTGGTTTTATT | 10580 |
rs534513015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502151 | CACCTCAAAGCAGTA[C/T]AAAAGAGCAATTTCT | 10580 |
rs534531360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395413 | AGTATGTAATAAACA[C/T]GCTATCCTAACATGA | 10580 |
rs534535681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379249 | GCCGGGCATGGTGGT[A/G]CGTGCCTGTAGCCCC | 10580 |
rs534541780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485619 | TGGTGCCTTGTCTAA[A/G]TTAGTCAGTGGAACA | 10580 |
rs534542793 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352669 | ATTGGTATAAGTTAA[C/T]TTACTATCCAGCCCT | 10580 |
rs534543477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354497 | CCAACAGAGGGGTGG[A/G]CAGTATTGGAGAAAT | 10580 |
rs534551841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549397 | CCCAGCATGGACGCT[A/G]GTCTATAACCGGTGC | 10580 |
rs534553837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394466 | CGGTGATACAGTCAG[C/G]AAGGAGTGAGACACC | 10580 |
rs534558437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358748 | CACACACACACACAC[A/G]TATTTCTCAGTTAAG | 10580 |
rs534567484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471595 | GGCATGGTGGTACAC[A/G]CCTGTAGTCCAAGCT | 10580 |
rs534571730 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530498 | AGAAACTAATCTAAA[A/G]TATCTCACTACAGAC | 10580 |
rs534582809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424439 | TGTTAATTCAACCAA[C/G]CGTGGATCAAATATT | 10580 |
rs534582915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515873 | ACCCTATGAGAGAGG[C/T]ACCTTCTGCACCATA | 10580 |
rs534586550 | in-del | -/CT | 0.00119808 | 0.024446 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369727 | CACACCCAGCAAGGG[-/CT]CTCTCACCACAGCCA | 10580 |
rs534593419 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410108 | CCAGTGAGTCTTCAA[A/G]AAAAATTCAATAGTC | 10580 |
rs534601648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372996 | ATTTCATTATAGCCA[A/T]CTCCATGGAAGCATT | 10580 |
rs534617308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359348 | CTTGAACTAGGCCAT[C/T]GAGCACTACACGGAT | 10580 |
rs534630412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409281 | ACAAGGAAGTTCAGA[G/T]AAACAAAATTTCACT | 10580 |
rs534649440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416812 | GAATGCTAAGGATTT[G/T]TGAATACACATGTGC | 10580 |
rs534670372 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514021 | CATTGACAAAATGCT[A/G]ACAGTCTGCCCAGGC | 10580 |
rs534691181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530189 | AGAATGCCTTCCAAG[A/T]CGCTGGTTCACCTGC | 10580 |
rs534703247 | snp | C/T | 4.95987e-05 | 0.00497965 | missense | SORBS1 | GRCh38.p7 | 10:95381705 | TTTCGTTGGTCAGAA[C/T]GGAAGACTTGCCAGG | 10580 |
rs534709156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487679 | ATGGGAAAACTAAGG[C/T]GCCCAACGAGGAGAT | 10580 |
rs534729325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516326 | CTCAAGTTTAAGAAC[C/T]AGTGTGTTGTGCTAT | 10580 |
rs534751154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516899 | GAGGGTTGGAACTCA[A/G]GTTGCATTTTCCCAT | 10580 |
rs534763365 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402061 | TTAAGATCATGGTGA[G/T]GATCACAGACATGCC | 10580 |
rs534770703 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403698 | TCCCAAGTAGCTGGG[A/C]CTACAGGCACGTGCC | 10580 |
rs534776725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480608 | CTGTGAACTATGAAA[C/T]AAATGACTTAGACTA | 10580 |
rs534807122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451278 | CAAAACATTTCATCT[C/T]AAAATAGTCAGCAGG | 10580 |
rs534826024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403016 | GTTTGAAGGAGGTGG[G/T]ATAGCTTCCCTTTTC | 10580 |
rs534826237 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523787 | ACATCAGGCTCCCCC[A/G/T]ATAAGCCATACCCCT | 10580 |
rs534828628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340157 | CTTTAGCAAGCCAGA[A/G]AATTTTGCCATGTAG | 10580 |
rs534829745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433513 | GAACGCCACAGTTTT[A/G]TTTTGTTTTCAAATT | 10580 |
rs534870435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517468 | TTAGGTCAAATCTCT[C/T]TAGTACCTGCTTCAG | 10580 |
rs534871068 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407048 | GATAAAAATAGAACA[C/T]TTGCCAACCCGTGGG | 10580 |
rs534893223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495699 | CCTCAAATTTCATGC[C/T]ACTCAGCTCAGACTT | 10580 |
rs534899316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318788 | ACCAGGGACTGGTTT[C/T]GTGGGAGACAATTTT | 10580 |
rs534925884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543810 | GGCCCCTCTGTAGGC[C/G]AGGCCCGTGCTAGGT | 10580 |
rs534949358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382125 | TTCGCTCTATGGGCT[C/T]TTCATTCCACAGACA | 10580 |
rs535000639 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464318 | GCGAGACTCTGTCTT[-/A]AAAAAAAAAAAAAGA | 10580 |
rs535001127 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446421 | AAAACAATCAACTAA[A/T]TATGGGTTGGTTACT | 10580 |
rs535004766 | in-del | -/AAC | | | utr-variant-3-prime, cds-indel | SORBS1 | GRCh38.p7 | 10:95312953 | CCTCAGAGACCGTAA[-/AAC]AACAACAACAACAAA | 10580 |
rs535005974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511234 | CTGAGCAACAGGATC[C/T]CATGCTGTTGCTCAG | 10580 |
rs535007355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417784 | TCACCACACCCAGCT[A/C]ATTTTTTGTATTTTT | 10580 |
rs535012260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375210 | AAGACTTTAAAATAA[C/T]TAGAGTTTTAAAGTC | 10580 |
rs535034501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404962 | TCCCCTTCCTGGGTT[C/T]CCTCCCTACTCTGAC | 10580 |
rs535037215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366373 | CTAACGTGAGCCTGG[A/G]TACAGGAAGGCTCCA | 10580 |
rs535064072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536908 | AAGGTCATCCTACTA[C/T]ATAGAATAAATCCAA | 10580 |
rs535066477 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333401 | GTATAAGCTTCTGCA[A/C]CCCATTGGTTGGGTC | 10580 |
rs535066707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431982 | CAGGAGCAAGATCAT[G/T]GAGTCATCCACACTT | 10580 |
rs535074352 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312973 | CAACAACAACAAAAA[A/C]AAAAAAACAGTGCTC | 10580 |
rs535079664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504585 | TTTTATACGTGTATC[C/T]CCGGACAAATCTTTT | 10580 |
rs535136128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544630 | TGCAAGACAGCCCAG[A/G]GAGGTCTGCACCCTA | 10580 |
rs535143203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347727 | AGGTGTGAACCACTA[C/T]GCCCGGCTGTGGAAT | 10580 |
rs535144286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558360 | TACAATCTATCCCCC[C/T]GAGTTCCCACCCCAG | 10580 |
rs535157900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388386 | CAAGGAATGGGAAAA[C/G]AGTGTAAGGAGCATG | 10580 |
rs535166603 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411977 | GCTATTTAGTTATGA[G/T]GGGCAGCTCAATGTC | 10580 |
rs535166681 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404368 | CAGTGGCATGAAGTT[A/G]CACAGAAATCATGTA | 10580 |
rs535176209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357303 | ATGGCTACCCTGCTA[C/G]AGTTAGGAATGGCTA | 10580 |
rs535179083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320994 | TTCTGTGAAAGTGAA[C/T]GTCTTAGACCCTCAC | 10580 |
rs535179283 | snp | A/G | | | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337247 | GGCTCGGCGGGAGTG[A/G]GGCAGAGATGAGGGG | 10580 |
rs535181552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326838 | GGACACTTGAGATGT[C/G]GCAAGTATGAAGTGA | 10580 |
rs535190491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557490 | TACAAAAAAACCGGG[A/C]CTTCAGCAGAACTGA | 10580 |
rs535194300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418474 | CACTGCAACCTCCGC[C/T]TCCCAGGTTCAAGCT | 10580 |
rs535209786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367131 | TCACTGCAGCCTCAG[G/T]CTCCTGGGCTCAAGA | 10580 |
rs535212529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361472 | CCCAAGAGCTCTACA[A/G]CAATGCTGTGTCGCC | 10580 |
rs535227226 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461281 | TCATAAGTAAAAATA[C/T]GGACCCAAAATCAGT | 10580 |
rs535232405 | snp | A/G | 1.78784e-05 | 0.00298979 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337115 | GTGGTCAGTGTTATA[A/G]ATAGAAGCCTCTGGC | 10580 |
rs535234267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459748 | AGGAAAGCAAAGGGT[A/G]ACCCAGCCATGGCTC | 10580 |
rs535242608 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489900 | GGCCATCCCACTGGG[A/C]TCTGTCTCAGTAGGT | 10580 |
rs535247431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426849 | GAGTGGTTTTGTGAA[C/T]CCCCTGAACTTGCAG | 10580 |
rs535248930 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433212 | CATAACAAAGAAAAC[G/T]CACAGCAACAAAAAC | 10580 |
rs535253107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532741 | GTGTCTGGATTAAGA[A/G]TGGCCCCATTGCACA | 10580 |
rs535256073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343164 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCCAGATT | 10580 |
rs535263323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320499 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 10580 |
rs535270932 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481091 | CTGCCAAGCACCCCC[A/C/G]GGGCCCCTGTACCTC | 10580 |
rs535301494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490137 | CACACTGTTATTAAG[A/G]ACATATTTTTGCCTC | 10580 |
rs535306548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427513 | ATTCAGAGATGAGGA[A/G]GCTGATCGGGAAGCT | 10580 |
rs535312182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531793 | TTGTTAGGATTTAAG[A/G]TAACATGCACAGGGG | 10580 |
rs535353435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334140 | TCTTGATACACAAAC[C/T]GGTCTGGAATGCATT | 10580 |
rs535402039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440153 | TGTCCATTTTGCAGA[A/G]GAGAAGGGTCCACCA | 10580 |
rs535403812 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379565 | AACCTCTCCTGCTAA[C/T]CATGCATAGATGTGC | 10580 |
rs535413263 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382735 | GCTCTAGTTTGCAAA[-/T]TTTTTTATTTGTGCA | 10580 |
rs535416552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559419 | CAACAAATGAAAGCA[C/G]GTAGGAGAAGGAAAA | 10580 |
rs535419207 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404838 | GCTTTCCTCACTTGA[C/T]AGTAAGAAAACTGAA | 10580 |
rs535422333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391518 | GTTTCTGCACAGTTT[G/T]CCCCCTCCCTTCTGC | 10580 |
rs535423435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446355 | TAAGTTTTGATGACA[C/T]AAAGTGATTAATTAC | 10580 |
rs535431232 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316791 | ACCATTTCTAATATT[G/T]ATTACATGTTCAAAT | 10580 |
rs535442050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348587 | CTCTTGAGACGTGTA[C/T]GTGAGTCATCGATGG | 10580 |
rs535442051 | snp | C/T | 0.000970991 | 0.0220126 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355590 | AGCAAAGTGGAGGGA[C/T]GGGCAGGTGAGACTA | 10580 |
rs535446941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397102 | TCAGGCAGACCAGTA[A/C]CTAATGAGGTCCAAC | 10580 |
rs535465484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322876 | AGGATTCAAAATAAA[A/G]GCATGAGCAAATCCA | 10580 |
rs535475873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558767 | AGAAGCCTGCATCCT[A/G]GAATGCTTCTTCTAT | 10580 |
rs535483600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461612 | ACACCAAGTATTAAA[C/T]GCTGATGCTCAACCC | 10580 |
rs535486505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360772 | CTGACAGCAGCTTCC[A/T]TTCTGCTGTGCCTGC | 10580 |
rs535506214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413504 | AGTGACCCTGGCCCT[A/C]ATTTGCCAGGGTAAG | 10580 |
rs535506682 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438049 | ACTTGCCTGGTGTGA[A/G]GATCCATGCTTAGCA | 10580 |
rs535515246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489523 | GAGCTCACATTCTTA[C/T]GTATCATTCCCACTC | 10580 |
rs535531611 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327328 | GAAGCAGGTGACAGT[C/G]CTTGATCCAGAAAGT | 10580 |
rs535535443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528287 | TCAAGGAAAACCAAA[A/C]CACAGAATAATAGAA | 10580 |
rs535535481 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551810 | TATTCAGAGAACTAG[C/G]GAGCTCTTACAAAGT | 10580 |
rs535538262 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386549 | GCTAAGGCAGAAGAA[C/T]TGCTTGAACCCCAGA | 10580 |
rs535547072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484626 | AATTCAGGGAACAAA[C/T]AAATACAATGTCCAG | 10580 |
rs535554039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355111 | TCGAATTCTGAAGGA[A/G]AAAAAAATTCCACCC | 10580 |
rs535556852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428200 | TGGATCATGAGGTCA[A/G]GAGTTCAAGACCAGC | 10580 |
rs535569947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496900 | TTGCATTTGCTGTTC[G/T]CTCTGCCTGCAAAGC | 10580 |
rs535572522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453342 | TGTTTTTTGTTTTGT[C/T]TTGTTTTGTTTTTGA | 10580 |
rs535591575 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461162 | ATTTTAAAATTATTC[A/T]CACATGTGCCCTTCA | 10580 |
rs535598943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335511 | AATATTCTCAGTTCT[A/T]GAAGCAATTCTAGAT | 10580 |
rs535613779 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332374 | ATTGTAACTATTTGG[A/G]AACAGGTCTTACTCC | 10580 |
rs535632766 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512351 | TTGAACCCAGGAGGC[A/G]GAAGTTGCAGTGAGC | 10580 |
rs535643107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547495 | CCCAGCACTTTGGGA[A/G]GCCGAGGGGGTGTAT | 10580 |
rs535646255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448380 | CACTGTGCTGGCACC[C/T]ACCTATGCACTCCCC | 10580 |
rs535648697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350994 | CCAGCAGATCCCGGT[A/C]CCCCAGCCAGGCATG | 10580 |
rs535655845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481489 | CTGTCCAGCACAACT[A/C]CCATAGCAACCCTCC | 10580 |
rs535696859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518793 | AGGGAAAGGAGACTG[C/T]TTACCATACATTTAA | 10580 |
rs535715283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455171 | TGGGAATAATAACAG[C/T]CATCAATCTCATAGC | 10580 |
rs535722164 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457032 | AAATTATCAGAAAAT[-/A]AAAGGTGTCGAAAAA | 10580 |
rs535731367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474794 | CGTTTTAATCTAAAG[A/G]TAACTGCCTAGGTGA | 10580 |
rs535732832 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495120 | TCAATCTCCTGATCT[C/T]GTAATCCACCCGCCT | 10580 |
rs535747443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492253 | CTTCAATACAAGACT[A/G]TAAATAAGTTTATGT | 10580 |
rs535762256 | snp | C/T | 0.000608088 | 0.0174262 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356807 | GTTCTCAATGCTCCC[C/T]CCCACTTGGAGGGGG | 10580 |
rs535765297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342472 | GTCTCATTCTGCTGC[C/T]CAGGCTGGAATGCAA | 10580 |
rs535768339 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314862 | AATTCTTTTTGCTCA[G/T]CACACTAGTTCGGCC | 10580 |
rs535772529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447573 | AGAGCCCCAGAATAA[A/G]TGCCTGGCCTTATTT | 10580 |
rs535774775 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455627 | ACTTTACCACTTCCT[C/G]CAGGATATACAGAAC | 10580 |
rs535780635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540801 | GGTCACTAGCCATCA[A/G]TTCCCTACCTTGAGA | 10580 |
rs535798655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482366 | AATATAACCCAGGAT[C/T]GTAAAATCCAAGTAT | 10580 |
rs535804594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412749 | CAAAGGGAAGATGCT[C/T]GAACTCCCCAAAACA | 10580 |
rs535816153 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486900 | GTGTGTGTGTCTGTG[C/T]GTGTGTTTAACTTAC | 10580 |
rs535833717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362512 | TTAAACTCAACGTGT[C/T]CCAAACCATCTTCCA | 10580 |
rs535834412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337597 | CAGAGTAGTGACGGA[C/T]GAGGCCGCCCTGCTT | 10580 |
rs535842230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369682 | ATCCTCAGTGACCTG[A/G]CTTGCATCTGCCCTC | 10580 |
rs535842439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512938 | TGATATTGGCAACTT[C/T]GGGGGTCAGGGCGAA | 10580 |
rs535849646 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314082 | ATGTCTTGCTTATGG[C/T]TGTCCCCCCAGCAGC | 10580 |
rs535855561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484081 | ATACAAAAATTAGCT[A/G]GGCATGGTGGTGCAA | 10580 |
rs535864870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467577 | AACCAAGAGGCGGGG[G/T]TCCATTTGAGAATCA | 10580 |
rs535894499 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410924 | TCGTATCATTAATTC[C/T]AGTTAGAAGTTTAAG | 10580 |
rs535918981 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506734 | TTATGCCAGAGCTAT[C/G]GGAAGAATAATTTGC | 10580 |
rs535921022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376844 | AACAAAGGGGAAAAA[A/T]ACTTCTGGGTTATAT | 10580 |
rs535922014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521110 | AATTACCACAGATGG[A/T]TTCTGAACCAGAAAA | 10580 |
rs535930473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476699 | AATCATTTTAATTAG[C/T]ACTTTCATTGTTTGT | 10580 |
rs535943792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392977 | GCCTTGAAGGAAACT[A/C]TTATCTTACGAGTTT | 10580 |
rs535944555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420394 | GGACATGCTTCTACA[C/T]TTGCTTTGAATTAAT | 10580 |
rs535964864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344636 | TCTTGAACTCCTGAC[C/T]ACAAGTGATCTGCCA | 10580 |
rs535978069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434953 | TGGTCAGTGTTGACC[A/G]GTGCCTCCTACCACA | 10580 |
rs535982644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505732 | AATTTTTCAGAGCAA[A/G]GGGTATTTAGAAGAA | 10580 |
rs535982980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513660 | AAGCAGGATTGCAAG[A/G]ATGGCAGGTGCAGGG | 10580 |
rs535989534 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484609 | ATGCTATAAATATGA[C/T]AAATTCAGGGAACAA | 10580 |
rs535991378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476201 | GCTGATGCCAATAAC[A/G]ACAATGATGACAGAA | 10580 |
rs536004990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407131 | TGAACCAGAAGTAAA[C/G]AGCGAGCAGCTCAGG | 10580 |
rs536006065 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467056 | ATCTCTATTTTTAAA[A/T]TATTTTCTTCAATGA | 10580 |
rs536018403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398653 | CTTACCCTGGACCAG[A/G]AATTTCTCAACATGC | 10580 |
rs536021980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540258 | TGGCAGCCGCAGCCG[C/T]GTTTTAGGTAAGTGT | 10580 |
rs536024258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415060 | AGGGAACCCCATCCA[A/T]CTCCGCTTTTCATCC | 10580 |
rs536025504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357469 | GAAAGAAAAATGGCC[A/G]GTAAGAAAATAGGGG | 10580 |
rs536034095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441061 | GGGCCTTCAGGGTGC[A/G]TGGGAAATCTGGGTA | 10580 |
rs536049002 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412612 | CTAAAACCAACTCGA[C/T]ATGAAAACCTAGGTC | 10580 |
rs536051284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364268 | AAAAACAGAGGCTTT[C/G]AAGACCTATTTTCAG | 10580 |
rs536051765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507340 | CTGGGATTACAGAGC[C/T]GCCACCACTCAGAAA | 10580 |
rs536066425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484382 | GCAAATTGGACTCCC[C/T]CCTGAGGGGGCAACC | 10580 |
rs536069993 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399274 | CTAGCTGGGGGGAAG[C/T]GTGTCTGCTAATTCT | 10580 |
rs536083085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546844 | TGGGTTCAAGCGATT[A/C]TCATCCCTCAGCCTC | 10580 |
rs536084110 | snp | A/G | | | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95387065 | AGGCTGCAGTGAGCT[A/G]TGACTGTACCACTGC | 10580 |
rs536092303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408165 | AGTTCTCAATGTGGT[C/T]GGTGGGCCAGTGGCA | 10580 |
rs536127938 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334223 | GAGAACAGTTGTCAT[A/G]CAAGTCCTTCCCATT | 10580 |
rs536129694 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535090 | TGATGGGTGGAGAGA[C/T]GGATGGATGAGTAGA | 10580 |
rs536132332 | in-del | -/TTATTA/TTATTATTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342863 | TCAATAATGATGATG[-/TTATTA/TTATTATTA]TTATTATTATTATTA | 10580 |
rs536164163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533636 | AAAAGGCTGCTTCTG[A/C]GTGGTTTTAGGAAAC | 10580 |
rs536172736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508326 | TTAAATCTCCAGGAA[A/G]CTGCTTCCTAAAAAA | 10580 |
rs536185879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491424 | TGTGGAAGTGTTACA[C/T]TTCATCTATGGATAT | 10580 |
rs536207964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401078 | ATTCAAGAGGTCAAA[A/G]GATTAGGGACAAAAA | 10580 |
rs536223504 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369270 | TAGTTCTTGGTTTCA[C/T]ATCCTTTCTCTCAAC | 10580 |
rs536230120 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429158 | TTACCTATACTCACA[G/T]CCTCATTTTTTTTTT | 10580 |
rs536238306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534894 | GCACCCTCCACTCTG[G/T]GCTTCCCCAACACCC | 10580 |
rs536241970 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394274 | GCTTCCCTGAGTCAC[A/T]GCTCAACCACCAGCA | 10580 |
rs536294106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338465 | TCAACTTTGGCCAAG[A/G]TGACTGAGGACCGCA | 10580 |
rs536298172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514490 | CTAAGAGATACTGTG[A/G]AGATCAAGCCAATTC | 10580 |
rs536298982 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534260 | CGGTGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 10580 |
rs536303287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434230 | CAGCTAAGTTCAGAG[A/G]TTCTCTGTGAGACCA | 10580 |
rs536307460 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458046 | GCATTTCAGGGCTGG[-/A]AAAAAAACACAGTTT | 10580 |
rs536322461 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408382 | CAGACAGATGGTAAG[C/T]GATTTGTCTTCATAC | 10580 |
rs536327113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485704 | TCCTTGTTTTAGTGA[C/T]GACCCCAACACAATT | 10580 |
rs536332172 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368386 | ACCAAGAGCTACATG[-/C]AGAGAAAAAGCAACA | 10580 |
rs536332772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469412 | CTTAGATTAGCTAAG[A/C]CAACATTTCCCAAAA | 10580 |
rs536356856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535722 | AAAGAAGGTAAACCG[G/T]AACTGCTCTGGACAA | 10580 |
rs536408496 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561631 | CCCGCCGGCCTCCGC[C/T]GGTAACGGGCGCGCG | 10580 |
rs536413214 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512510 | TTCTGAATCGAGGAT[A/G]TAAATCTGATCTAAT | 10580 |
rs536427974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430713 | TCTTCTCCAAATGCT[C/G]TCTAGCTTGGAAGTG | 10580 |
rs536449276 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464338 | AAAAAAAAAGAAAAA[A/T]AAAAAAGGCTCAAAT | 10580 |
rs536451175 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538176 | CAGAGAGCTTCATGA[A/C]AGAGGCCTTGGGGTG | 10580 |
rs536456161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317016 | AAAGTAGTGAGGGCC[A/G]TGGGCTTCTGAGGAC | 10580 |
rs536472380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560864 | TGCAGAGGTGCCCCT[A/C]CTCGGTAGTTTCACT | 10580 |
rs536473710 | snp | C/T | 0.000185374 | 0.00962562 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415914 | GTCCTGGTGGCTGCA[C/T]AGCGCTGCTGGGGTT | 10580 |
rs536490227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424593 | CAGGAGATCTGCATA[A/G]GTTATGTACAAATAC | 10580 |
rs536494487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528684 | AGCACTTTGGGAGGC[C/T]GAGGTGAGTGGATCA | 10580 |
rs536497457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516367 | ATGAACCACGGTGGT[A/G]GATCAACAAAAGTAG | 10580 |
rs536501220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436728 | AAGCAGAAATAAATA[A/C]GGCAGATCATAAATT | 10580 |
rs536524191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462748 | TTCTTTGGTCAGGGA[C/G]GGGGCATATACACAA | 10580 |
rs536530191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386716 | CAGCACTACTTGGGA[A/C]GTTTAACAATGTATG | 10580 |
rs536533232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323897 | GGGATCAACTGAGCC[C/T]GGGAGATTCAGGCCA | 10580 |
rs536536181 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509169 | GTACATCACCAAATA[G/T]GAACAGAAGCCGTCT | 10580 |
rs536545458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555278 | CCAGTCCTGGTGGGG[A/G]GTGCAGGGGGGCCTG | 10580 |
rs536546695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548060 | GAGGGGAGAAGAAAT[A/G]CATGGGGACAGGGGA | 10580 |
rs536546906 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366091 | TCAGCAACTCTGCTC[-/A]TTGTGGATTTATCCA | 10580 |
rs536574538 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534987 | GAGACTCAACATCTC[A/G]TTCATCCTCACATAT | 10580 |
rs536580042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515656 | TCTCTTAGGATGAGG[A/G]ACAGGATATGAGACA | 10580 |
rs536585682 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364148 | AATCTTATTCATTTG[C/G]ATAAACTGGGGGAAA | 10580 |
rs536589030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380236 | GAAAAACTAAACTAT[A/G]TTGTTTTTCCTAGTT | 10580 |
rs536606763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556748 | TAGAGACGGGGTTTC[A/T]CCATGTTGACCAGGC | 10580 |
rs536607742 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439935 | TAGCCAGGCGTGGTG[A/G]TGGGCACCTGTAATC | 10580 |
rs536619774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326157 | TTGCTTGTGTAACTA[C/T]GACAGCAACACCCAA | 10580 |
rs536620053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318883 | TCTCATAAGGAAGGC[A/G]TAACCTAGATCCCTC | 10580 |
rs536636631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359404 | ATTTTACTGCTCATT[A/C]ATTTATTTTTTTGTT | 10580 |
rs536669050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556094 | AAGGAAGTCTAGAAA[C/T]AGGGTACATCCCTTG | 10580 |
rs536678360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346133 | GAATTCCAACTCTAT[C/T]ACACCAGCTTGAGCA | 10580 |
rs536703808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364759 | GCCAGGTCTAAATTG[G/T]TTTTTAATAGCTTGA | 10580 |
rs536710257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457248 | ACACCATGTTGGAAG[A/G]AAAGAACTATGTATT | 10580 |
rs536721876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465000 | GGAATGAAACAAGGG[C/T]TCTACCTTTCAACAC | 10580 |
rs536727445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494630 | CTTCAGGCAGCCAGC[A/G]CCAGAGAAACCCACA | 10580 |
rs536735903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325551 | CCATCCCAGGCACTA[C/T]TTCTTTTTTTTTCTT | 10580 |
rs536750172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416954 | CAATGAAGGACTGAA[C/T]TGGCCTCTACCGGAT | 10580 |
rs536750910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425021 | AACACCTGGTGACAT[A/G]CCATGACAATGGTCC | 10580 |
rs536763832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543004 | CATTTGCACCACTGC[C/T]AGACTATGCCCATGC | 10580 |
rs536768015 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358716 | GACATGCGCGCGCGC[A/G]CGCGCGCACACACAC | 10580 |
rs536784119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457970 | TATCCATGTAATACA[A/G]CTGTACTTGTACCCC | 10580 |
rs536787521 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371498 | AAGAATGGAAGGTTA[C/T]GTTTGAAAAAAATGA | 10580 |
rs536811659 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337580 | TGGGGAGAGGTTCCC[A/G]TCAGAGTAGTGACGG | 10580 |
rs536832419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522213 | CCCAACCGAAAGGTG[C/T]CTCCTTTTCTCCCTT | 10580 |
rs536837674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445722 | GTTGTGTCTCTACAA[C/T]CTTAAGTGCTCAGAG | 10580 |
rs536841771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347761 | TTTCTTTTTTTTGAG[A/G]CAGCGTCTTGCCCTG | 10580 |
rs536842020 | in-del | -/AAAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407961 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GACTATGTTGTCTCC | 10580 |
rs536844919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438249 | TTCCTCCCCAAATGG[A/G]ATAAACATTTGGGTT | 10580 |
rs536855914 | snp | A/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442819 | AAAGTTTAAAACCAC[A/C]TTAACAATTTCTACC | 10580 |
rs536859128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495768 | GCTTTCCGAGCTCAC[A/G]ACATACTCTCTTCTC | 10580 |
rs536873682 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410456 | GATCAGGGGCCTCTG[A/T]CTGTCTGCTGGGATT | 10580 |
rs536873805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388708 | AGGAAGCTGTAACAC[C/T]GCATGGGATTTACAC | 10580 |
rs536879202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341026 | TTGTATTTTTAGTAG[A/G]GACGGGGTTTCACCA | 10580 |
rs536887257 | in-del | -/TCT | 0.0458263 | 0.144267 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369328 | CTCCCTAGTTGGGTA[-/TCT]TCTTCTATCCCCAGG | 10580 |
rs536894998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332668 | TCGTCATGCTGGCTG[A/G]TCTTGAACTCCTGAC | 10580 |
rs536900162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418357 | TGCTGGGATTACAGG[C/T]GTCAGCCACAGCGCC | 10580 |
rs536911415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451453 | ACAGTTTCTAAAATA[C/T]GCAGTTAACCAAGAC | 10580 |
rs536934185 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471626 | ACTTGGGAGGCTGAG[C/G]AGGAAGATCAGCTGA | 10580 |
rs536945062 | snp | G/T | 1.6922e-05 | 0.00290873 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371465 | GGAAAGAAGGTTTTA[G/T]TTTAGAGGAAAGGGA | 10580 |
rs536966756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346812 | TGTTCCTTATCTACT[A/G]TCTTATTCCTTAGAG | 10580 |
rs536970682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437347 | GTCTCAGAAAATCAG[C/T]GTAGGGAACAGGTCA | 10580 |
rs536975972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445188 | ACACGAGGACTTTTT[G/T]AGTAGCAGGTTCTGT | 10580 |
rs537010368 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363839 | AAAACAACACCATCA[C/T]TTCTCCAGTTGCCAC | 10580 |
rs537017081 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511462 | TTAATCGATCCTCCC[A/G]TCTTGGCTTCCCAAA | 10580 |
rs537036811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509827 | CAGCAGGGGGCTAAC[A/G]GTGACGGTGTCGGAG | 10580 |
rs537047141 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361641 | TTTGTAGTTTTAGTA[A/G]AGACAGGGTTTCATT | 10580 |
rs537051789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459081 | TTAAGAAGCATGTAA[C/T]TGTAGACTTTTTTCC | 10580 |
rs537058623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382848 | TATATCCTTCCATGA[C/T]ATATGGTTAAATCTG | 10580 |
rs537060729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480769 | AGGCACAATCTTGCA[C/T]CCAAGGAACCTTCCA | 10580 |
rs537071316 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391560 | CCATCCCGTAGACAG[C/T]AGTCTCCAAGATTAC | 10580 |
rs537084517 | snp | C/G | 1.64963e-05 | 0.00287192 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410593 | TGGAATAGCTATGTT[C/G]ATTCCAGTGGGCTGG | 10580 |
rs537095180 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335085 | TAAACTGCCCCATGC[A/C/T]GGCTCACCCTCAGTG | 10580 |
rs537110142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502910 | TCTCCCTCCTCCTCT[C/T]CTTTGGCCTCCATTC | 10580 |
rs537115461 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329979 | CCTTTAGGAACCAAA[A/C/T]TGACATCACAAAATT | 10580 |
rs537137835 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466208 | GCACACTGGGAGGCC[A/G]AGGTGGGCTAATCAC | 10580 |
rs537164110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517615 | TTTCTGCTCATCAAT[C/G]TATCTTCCCCTGGTA | 10580 |
rs537171567 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510387 | AGAGTGCAGTGGTGC[A/G]ATCTCAGTTCACTGC | 10580 |
rs537173228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374080 | AGGTTGTTAGAGCAA[C/T]GGGGTGGGGAGACAA | 10580 |
rs537177389 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490211 | TAATTAAGTTTCTTT[A/C]AAAAAAAGGAAGAAC | 10580 |
rs537187412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465453 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC | 10580 |
rs537203855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403929 | CTGTCACAATAACAC[C/T]TCCTCCAGGCTGGGG | 10580 |
rs537222629 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544314 | GCCTCTAAGCCAAGC[A/G]GAACAGGTGGGCTCT | 10580 |
rs537247790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461042 | AGAGATTTTCTCAAA[G/T]GCAAGTTTTCTTATT | 10580 |
rs537254782 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515159 | AGACCCCTGCATCAG[A/G]ATTTCTGCGATCTCT | 10580 |
rs537302957 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385006 | AGTATCTAAACTGCA[C/T]CTCTGGAGCAAATCA | 10580 |
rs537310938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497049 | CTTTCCTTGTAGACC[C/T]TCTCACAATCTGTAA | 10580 |
rs537311005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505538 | AATGAATGTGGAGGA[C/G]ATAGATGAATGTCTA | 10580 |
rs537318224 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342112 | CTTCGTTGCTTTAAA[G/T]TGCCCTCAAATTATT | 10580 |
rs537328579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488673 | TAGGGTCCCTCTTTG[C/T]TCCTTATCTCAGTGA | 10580 |
rs537331211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327700 | CCTCTAGAAACAGCA[C/T]GAGGCTCTGCTGCTC | 10580 |
rs537333422 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95478660 | AGTAGCTCAGATGAG[C/T]GTAACTTCACAGACA | 10580 |
rs537340639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403144 | CCAGCCCTTATCTTA[C/T]TATCCCATCCATCTC | 10580 |
rs537359190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354556 | AAGGGTGGGGTTGAG[C/T]GGGGATGAAAGAGCA | 10580 |
rs537370350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512593 | CAATTTCAGCCACAG[C/G]TTCCTGGTTAGATGC | 10580 |
rs537374654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504751 | ATCATATAATTTTTC[A/T]GGAAAAAGTGTCCAA | 10580 |
rs537380684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367801 | AAGAGAGAGGTCAAT[C/T]TCTTTTTCCTAGTTT | 10580 |
rs537385479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496144 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGACCTCG | 10580 |
rs537409578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334431 | CCCAGGCCACAGCCT[A/G]TGCACACCCATGGAG | 10580 |
rs537409903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397697 | CAACAGCAATGTATC[C/T]GAGTCACCTTGCATA | 10580 |
rs537427217 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531638 | CATGGAGAAGCAGCA[C/T]GGACTTTCAACGAGG | 10580 |
rs537427550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524224 | GGCAATGTGCGTCCA[C/T]AATGACAAAGGCATG | 10580 |
rs537448321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497565 | CCAAGCCCACCCCTC[C/G]AACCATATCTCCAAT | 10580 |
rs537462498 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445402 | CAACGTCCTATCCAG[A/G]CTATTCCAGGGCCTG | 10580 |
rs537477871 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417905 | TTACAGGCGTGAATG[A/G]CTCCTATTTTTAAAG | 10580 |
rs537506769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439035 | AAAGCACTTCCCCCA[A/G]TGACTGGTAGCCCAG | 10580 |
rs537512774 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393635 | TCACAACTGCCCCCA[A/C]ACTGGACTCAGTCAG | 10580 |
rs537518525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491259 | CCCGATTTCCTTCCC[C/T]ACTCTGACTTCCCAA | 10580 |
rs537532508 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505857 | AAGCTCCAATCTGTC[A/G]TCCCTCCTGTATTCT | 10580 |
rs537534100 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537218 | ACTGCATTCATCCAA[C/T]AAATATGTACTGCCT | 10580 |
rs537540726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406024 | AGACATCAGAGGATC[A/T]TGGAAGATATTGCTG | 10580 |
rs537550861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356278 | CCATATTGCTACATG[C/T]TGGGGAAGCATAGAC | 10580 |
rs537566147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524849 | TGGGCACATAATAAA[C/T]ATCTGGTGAGTAAAT | 10580 |
rs537570053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432071 | GGAAGCAGGGATGAG[C/T]TCTGAGAAGCCCAAC | 10580 |
rs537596726 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447840 | CCCATGACACTCCTG[A/G]GAGCTCAGAACACAA | 10580 |
rs537596746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551274 | TGAGTGAAAGTCTGC[A/G]TATCAAACAGACTAA | 10580 |
rs537597836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382168 | CCATTCACACTAGAG[C/T]AGTGAGAGAGAACAC | 10580 |
rs537603547 | snp | A/C/T | 8.2383e-05 | 0.0064176 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336872 | ATCAGAGCTCCCCAG[A/C/T]GGCAGCTGCAAGAAG | 10580 |
rs537606353 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315737 | TGCTGATCCTTAATC[C/T]AGTTCCTTCCCTTGG | 10580 |
rs537616802 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321062 | GCTAGGCTTCTTTAC[A/G]TGTATCTCTGTTGGT | 10580 |
rs537622756 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492595 | TGCACCTGTGTTATG[C/G]GAGCACTGAGCAGGG | 10580 |
rs537641047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511898 | TCTAAGAAGGGCCTT[C/T]TCCTTTTTCTGGTCA | 10580 |
rs537648589 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494641 | CAGCACCAGAGAAAC[C/T]CACAGCTGACTAAGG | 10580 |
rs537652636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377630 | GGTTTAAATCCTGAA[A/G]GAGAAGCCTTGCCCT | 10580 |
rs537684022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405097 | GCCACACTCAAGTGC[C/G]GTCAGCACAGAGGGC | 10580 |
rs537698298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533272 | AAAACATAGCCAATC[C/T]GACTTAGGGTTTCTG | 10580 |
rs537699530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520245 | CTTGAACCCGGGAGG[A/T]GGAGGTTGCAGTGAG | 10580 |
rs537727754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320525 | GCTGGGACTACAGGC[A/G]CATGCCACCACGCCC | 10580 |
rs537730110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545042 | CCTGCAAAGCAAACA[C/T]AAAATAGTCCTAAAA | 10580 |
rs537734902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392170 | GCTGGAGCAGCACCA[C/T]GGACAGGGCTGATGA | 10580 |
rs537761735 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519442 | GAGTCACAAAAGAAC[G/T]GACATCCATTTTTAT | 10580 |
rs537800026 | snp | A/G | 0.000196734 | 0.00991607 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384420 | ACAGAAGAGTGAAGC[A/G]CCAGAAGCTACACCA | 10580 |
rs537803396 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543157 | TGCCCTTGCATGTGC[C/T]GGTCCCTCTGTCCTC | 10580 |
rs537851030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455659 | CGTCTTCCACATTGC[A/G]TGTGGCAGCTCATGC | 10580 |
rs537858594 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315746 | TTAATCTAGTTCCTT[C/G]CCTTGGGATTCTCTC | 10580 |
rs537866705 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552945 | CAAGCGCAGGCACGG[G/T]GGCTCATGCCTGTAA | 10580 |
rs537900771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446403 | ACTCATGCTTCCAGC[A/T]GAAAAACAATCAACT | 10580 |
rs537934979 | in-del | -/GTTTT | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433508 | ATGCAGAACGCCACA[-/GTTTT]GTTTTGTTTTCAAAT | 10580 |
rs537937479 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314003 | CACAACCCTGGTTAC[A/T]ACCGTTTGTGTGATC | 10580 |
rs537938317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547545 | AAGACCAGCATGGCC[A/C]ACATGGTGAAACCCC | 10580 |
rs537939448 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561809 | TACCCATCTGTAAAA[C/T]GGCATAATAGTCCGA | 10580 |
rs537945367 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349468 | ATTTGAGACAGCCTC[A/T]AATTTCTTTAAATTT | 10580 |
rs537955149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421723 | GAACAAACCTAAATA[A/G]GCATCAAGGCCTATT | 10580 |
rs537958116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532851 | CCTGTGCAGGCTAGA[C/T]AACTCCATCTTGAAT | 10580 |
rs537989539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462606 | CTATATAAAGAGTTT[C/T]CCAGACTTCAGAAAT | 10580 |
rs537992492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475409 | ACCTTTCAGAACTCC[A/G]TTTTTCCCCCTCAAA | 10580 |
rs538005187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328515 | CTTCTCTTCATAGAC[C/T]ATCATACAGTCTTCT | 10580 |
rs538011012 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467963 | AGTGCAATGGCATGA[C/T]CTCATCTCACCACAA | 10580 |
rs538042736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396132 | GGCGGCACAGGCAGC[A/G]ATGGGAGCCGGTGGG | 10580 |
rs538048884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519798 | CCTGAAGCTGCCTCA[C/T]AGCCTTGGTCCTGCT | 10580 |
rs538078208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337672 | CCAGCCAACCCAGCC[C/G]CTGTGCATCCAGATC | 10580 |
rs538090271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441008 | AAGCTTTGGCATTCA[A/C]CCAGGTGGCAAAAAA | 10580 |
rs538109527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448436 | TTTCAATGGGGAAAA[A/G]AACTCCGCAGGGCTC | 10580 |
rs538113343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357572 | TTCACCACGGCCGAC[A/G]CTCAGTGAATGGAGG | 10580 |
rs538121379 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95359056 | TACTCAACCAGCAAC[A/G]ATCAATAATGTGATG | 10580 |
rs538124405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559514 | AGACAGCAGTTCATT[G/T]CAGTTGCTAATTCCC | 10580 |
rs538125786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479945 | GACACAAAATGGTTC[A/G]GAGACATGCCCACTC | 10580 |
rs538140403 | in-del | -/ATCC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543279 | ACCCTTTCGACTATA[-/ATCC]TAGCTACTCAGGAGG | 10580 |
rs538157555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535016 | ATCTAGCACAAGTCC[C/T]GGTACAAGGAGGGAC | 10580 |
rs538161803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351655 | ACCTACCCCCGGCTC[A/T]GCCCAAAGCCTCTTG | 10580 |
rs538175455 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545038 | AGGCCCTGCAAAGCA[A/C]ACACAAAATAGTCCT | 10580 |
rs538200133 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470361 | TTTGGAAAACACTCT[A/C]ATTCTTACATTTAAA | 10580 |
rs538222405 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494475 | GGTCATGTAACGACC[C/T]GAGCAATCTCAAGCT | 10580 |
rs538233401 | snp | C/T | 0.000235294 | 0.010844 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357029 | ACACACAGGGCCTAA[C/T]GCATTGCTAGTGTTA | 10580 |
rs538267759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371488 | GAAAGGGAGAAAGAA[C/T]GGAAGGTTACGTTTG | 10580 |
rs538272113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476881 | AATGGAATTAAGGTG[C/T]TTTTCTTAAGCACCT | 10580 |
rs538276414 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395932 | TGTTAGCTGGCATCC[A/G]CAGCTCATCAGAGAG | 10580 |
rs538296446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324289 | AAAAAACCCAGGAAG[C/G]TGATGCTCAGAGGGG | 10580 |
rs538305791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499354 | TGGGATTACAGGCAC[A/G]AGCCACCATGCCCGG | 10580 |
rs538311129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461860 | TGGCACAGGGTTTCC[A/G]AGTGAGAAGTTTACT | 10580 |
rs538342122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413629 | CTGTGAGTAGATTCA[C/T]GTATTCCCATATTAC | 10580 |
rs538363965 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429641 | AAAGGGATTCCATTT[C/G]TTAGGCTAATTTCCA | 10580 |
rs538370855 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455215 | TTAAATAAGATTCAG[A/C/T]ACATCCAGTGCCTAT | 10580 |
rs538373259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370479 | AACTCCTGACCTCAA[C/G]TGATCCACTTGCCTC | 10580 |
rs538377065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362833 | TATTAAGTGTCAATC[A/G]CTCTCCTAGGTGAAG | 10580 |
rs538391987 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471583 | AAAAATTAGCTGGGC[A/G]TGGTGGTACACGCCT | 10580 |
rs538398521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534317 | CTGTGCTGGCCAAGC[C/T]GGTCTCAAATGCCTG | 10580 |
rs538417345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435066 | GGGTCCACAGGGCCT[C/G]TTGGGAGAAGGCTGG | 10580 |
rs538427143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352404 | CTTAGCATTGGAAGA[C/T]AGTAGGCTTCGTCCA | 10580 |
rs538442666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500235 | CATAGCCATTTCCAA[A/C]CAGGTTACACAAAAA | 10580 |
rs538444399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509068 | GTTCCTGAGATTGGA[C/T]TGTAGCAGCCCTTCT | 10580 |
rs538446647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492542 | AAATGCTCTACCCCT[A/G]AGCTAAACCCTCTAC | 10580 |
rs538454289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450041 | TTTACTTAACCCAAC[C/T]AGTTAAAAAATATAT | 10580 |
rs538461132 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393758 | TGGCACACAGCAAGT[C/G]TTCAATACTACTTGA | 10580 |
rs538465256 | in-del | -/TTT | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460163 | ATTGTTTCAGCAGGG[-/TTT]GAAAAAGAAACACCA | 10580 |
rs538510077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502036 | ACAGATCGATTCGAC[G/T]CCAGGAGGCACAGAC | 10580 |
rs538512058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494144 | CAAATGGGTAAGTGA[A/G]GTGGCCTTCCTCTTT | 10580 |
rs538518212 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464516 | GCACCTGGCAGAGTC[A/C/G]GGGATGGTGCAAGTG | 10580 |
rs538545540 | in-del | -/AACT | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428055 | CTCTTGACCTGCAGG[-/AACT]AACTAGAATGGTTAC | 10580 |
rs538565790 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407491 | AGGCGTGGTGGCACA[C/T]GCCTATAATCCCAGC | 10580 |
rs538572646 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484228 | ACTCCATTTCAACAA[A/C]AAAAAAGGTTGTTTT | 10580 |
rs538574044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501148 | TCCCAGAGATTCAGA[C/T]TCTGTCCACCTGGTA | 10580 |
rs538575709 | in-del | -/AGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374713 | AAAGAAAGGAGAGAA[-/AGG]AGAAGAAATGAGGTG | 10580 |
rs538577516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554589 | GAATCGCTTGAACCC[A/G]GGAGGTAGAGGTTGC | 10580 |
rs538584043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477625 | TAGAAAATCTTTTAA[A/G]GGGCTGCAAAGCACT | 10580 |
rs538585188 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493059 | GCACTTTGGGAGGCC[G/T]AGATGGGTGGATCAT | 10580 |
rs538591064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457303 | TACAGCAGGGGCCAG[A/G]GAGGGAGTGTGTTGA | 10580 |
rs538614311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528411 | ACAGTGCTGTGCCTG[A/G]CCCAGCCCTTGTCCA | 10580 |
rs538679468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423621 | CACTGCCCAATCCTC[C/T]GTTTCAATGTGGGTC | 10580 |
rs538701312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430897 | GGCTGTGGGCTGCTC[A/G]GGCCTGCCCTCAGCC | 10580 |
rs538719503 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386149 | ATAGCTTATCAGTAG[A/G]TGATAAGATGAAGGT | 10580 |
rs538738610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479156 | GGAAATGAGTAGATG[C/T]CAAGCAGAGAATATA | 10580 |
rs538759898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529234 | TTCAGCTCTTAAACA[C/G]ATTCTGACAGCCACA | 10580 |
rs538765029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560999 | CTACCCCACACCCAC[C/G]AAAAAAGGAAATTTA | 10580 |
rs538781426 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555838 | AGTTAACAAGCATCT[A/C]ATTCTTTTCCAAAAG | 10580 |
rs538788342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548827 | AGATAGGTGCTATTA[C/T]TTCCTCCATTTCACA | 10580 |
rs538807593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325613 | CTCTGTTGCCCAGGC[A/G]CAATCTGGGCTCACT | 10580 |
rs538849846 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431506 | CAACTACCAGAATAC[C/G/T]TGGGCTGTGCAAAGT | 10580 |
rs538859672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409778 | AACAAGCCCTTTCTA[C/T]ATGAGGAAACAGCTT | 10580 |
rs538893870 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523025 | TGTGTCAGAAATAAA[A/C]GTGTAAACATTTTCT | 10580 |
rs538908740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517420 | CTTCAGCTCACTTGC[C/T]GCTTCTTTGGGAACC | 10580 |
rs538919791 | in-del | -/CCACATGCAA | 0.0894459 | 0.191631 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488754 | GTTTTTACTCACATG[-/CCACATGCAA]CCTAGAAGGCTCTAC | 10580 |
rs538922229 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538547 | TCCCCACATTTGTGC[A/G]CTATTCTCCAAGTGG | 10580 |
rs538923621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542479 | GCCCAGACTGAGTCA[A/T]ATGACCTCTTATCAT | 10580 |
rs538926413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510629 | ATCAGTCAGTATCAA[A/G]CGTTCATTCTAAAAG | 10580 |
rs538931029 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316660 | TAAAATGATAGCCAC[A/G]TGTGACTACTGAGCA | 10580 |
rs538938977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556820 | CCTCCCAAAGTGCTC[A/G]GATAACAGGCATGAG | 10580 |
rs538950817 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509669 | GATGAGAAGGGAAAG[A/G]AAAAGAGAACCAAAT | 10580 |
rs538960750 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517533 | TGATTATAATGTTAC[A/C]CTCATTTGCTTAATG | 10580 |
rs538970631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516861 | ACAAACAGGCCATGC[A/G]CCAAAAGTTCATTTT | 10580 |
rs538971832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424683 | GGAACCAATCACTGG[C/T]AGATACTGAGGGACA | 10580 |
rs538984076 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541152 | CAGGGCTGCAATGAC[C/T]GCACTGAGATGAGAT | 10580 |
rs539003105 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411360 | TGTGACATTTTTTTC[A/T]CTCTAATATTAAAGT | 10580 |
rs539007826 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557062 | GTCCACATGCCTAAC[C/T]GCACACAAAAAGGGG | 10580 |
rs539009649 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311642 | GTGTCTTCAAGGAGG[C/T]GGCAGAAGGCAGATG | 10580 |
rs539010538 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559436 | TAGGAGAAGGAAAAG[A/G]CCAACAAGGCGGGTA | 10580 |
rs539014166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346863 | TGATATGCAAGTAGG[C/T]GAAATGCCGATTCAC | 10580 |
rs539020465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403475 | CATCAGCAGATCTGT[C/T]CCAAAACTCAGAGAA | 10580 |
rs539039671 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372457 | CATTTTTGAGGCAGT[C/G]TTCTGCTGTAAAATT | 10580 |
rs539059622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503057 | GTTCTCTAATTCAGC[C/T]TCTACTCATTGCCCT | 10580 |
rs539075757 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330264 | CTAGGAAGTACTCTC[A/C]CAATTTGTAAAAACA | 10580 |
rs539085401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450565 | GGAGTGCAGTGGCAC[A/G]ATCTCTGCTCACTGC | 10580 |
rs539097273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443361 | CTCGGGAGGCTGAGG[C/G]AGGAGAATTGCTTGA | 10580 |
rs539111494 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407667 | ACGTTGGCCAGGCAC[A/G]GTGGCTCATGCCTAT | 10580 |
rs539116422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401839 | AGATTGGCTTTATGG[A/C]ATGAGTTCTCATGCT | 10580 |
rs539126615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353602 | ATCTCCCAGGTTCAA[A/G]CAATTCTCCTGCCTC | 10580 |
rs539156247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396415 | CCTGTGACATTCTCC[A/G]GAGGAAAGGAAGCAG | 10580 |
rs539165248 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313742 | CCTGTGTCAGTCTCC[C/T]CAATCACCTCTGAGT | 10580 |
rs539168310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499337 | TTCAGCCCCCAAAGT[A/G]CTGGGATTACAGGCA | 10580 |
rs539211967 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326345 | TGGTCCACCTTGTAC[C/T]TTCCTTGGTCTCAGG | 10580 |
rs539234059 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374122 | GCCCCAGTATACAAC[G/T]GGACTGTGTTCTCAA | 10580 |
rs539236504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479912 | CAGCAGATATACTTT[C/G]GTTTGTTTTTTTTAA | 10580 |
rs539236747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439622 | TACTGGCAGTACCCG[A/G]GCCTGCTTAGAGGGG | 10580 |
rs539243431 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432113 | CGCACCGCTTACTTA[A/C]CCCCCATGCCCTAAG | 10580 |
rs539243793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465487 | GAACTGAGATCACGC[A/G]ACTGCACTCCAGCCT | 10580 |
rs539249319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348997 | ATTTTCAGGCCCCAC[C/T]GCAGAATCAGAAACT | 10580 |
rs539273841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544982 | CCTCGCCCCCTCACA[C/T]CTGCCATTGCTGGCT | 10580 |
rs539275420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334483 | CAGGAGGAAGGGAGG[A/G]GACAGGAAGTGGTAC | 10580 |
rs539298002 | snp | C/T | 0.000230833 | 0.0107407 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441084 | TCTGGGTAAACTGCC[C/T]AGTTTGGTAGATAAG | 10580 |
rs539356861 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340837 | AAAGTGCTGGGATTA[C/T]AGGCCTTAATGCAAT | 10580 |
rs539369613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550594 | ATGTTTGGGTGTCTT[A/G]AAATCTGATGACTAA | 10580 |
rs539371470 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367563 | TACAAACAAAACACA[C/T]TCTGGGTCCAAAATA | 10580 |
rs539406955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474721 | ATAATATTTATGTTT[C/T]AACCCCTCATGTGGC | 10580 |
rs539418150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511143 | CACATTTGCAGAATC[A/G]AATTAAGTGCTCCTT | 10580 |
rs539437325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360641 | CTGCCCATGTTGCTG[A/G]GTGAAGCTCTCTGAA | 10580 |
rs539459918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376747 | TGAATACAGACAGAA[C/T]ATACTTCGTGTTTTA | 10580 |
rs539460366 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458383 | TTAAAAAGGAAAAGC[A/C]AGCAGTTGAGAATTA | 10580 |
rs539469182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466131 | CCAGCCTGGGCAACA[A/G]TGCAAGACTCGAAAA | 10580 |
rs539498332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319967 | GCCCTTTAACTCCCA[A/C]CATGGCTGCTTTGCC | 10580 |
rs539512787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496178 | TCCGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 10580 |
rs539556031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504033 | TTAATAACAGAAAGA[A/C]GTGCACACTATAGCA | 10580 |
rs539559065 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548928 | TTTGAACCCAGGCAG[C/G]CTGAGTGCAAAGACT | 10580 |
rs539563297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335226 | TGCCTCTATTATTGC[C/T]CTGGTGATATTGCTA | 10580 |
rs539566973 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327707 | AACAGCACGAGGCTC[-/A]TGCTGCTCCCCTAAC | 10580 |
rs539572850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512052 | CACTCTTTGAAGTGT[A/G]AGCTCTCTCTCCCAG | 10580 |
rs539577580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367072 | TTTTTGGGACACAGT[A/C]TGGCTCTTTCACTCA | 10580 |
rs539586985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558247 | TGAGCCATGATTGTG[C/T]CACTGCACTCCAGCC | 10580 |
rs539593456 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460416 | CAATTGTCAGTCCCT[C/T]AAAAATATCTTTAGG | 10580 |
rs539598306 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350725 | ATATTTCAAAATTAA[-/T]TGTCACTAAATTTGG | 10580 |
rs539612541 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501714 | CCAGCCTGGGCAGTA[C/T]TGCATGACCCTGTCT | 10580 |
rs539618422 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474644 | GGCAACAGGAAGGAA[C/T]TGAATTCCACAGCTC | 10580 |
rs539647577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496792 | CAGTGTAGGGCCAGA[C/T]CTCCAGAAACCTGCT | 10580 |
rs539663272 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541946 | GCCTAAGCCTGTTGG[C/T]CTCCTGGCTGTGAGT | 10580 |
rs539665929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390578 | GTATTTCCCCATCCC[A/G]GTGGTTCTCAATCCT | 10580 |
rs539700025 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481400 | TCTTCCTCAAAGCCA[C/T]AATCACATCCCTCCC | 10580 |
rs539714220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461074 | ATATTGAGAAAGTAT[C/T]TTAAATGACTACTTG | 10580 |
rs539718455 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462719 | TATACCACTGTGCAA[C/T]ATGCAAACTTTTTTT | 10580 |
rs539719986 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361602 | AGGTGCCTGCCACCA[A/C]GCCTGGCTAATTTTT | 10580 |
rs539761015 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421884 | CTGGGGAAGCAGGAA[A/G]TCACCAGTCTAAGTT | 10580 |
rs539773863 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453386 | TCTGTTGCCCAGGCT[A/G]GAGTATAATGGCACG | 10580 |
rs539779188 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362506 | GGCATCTTAAACTCA[A/G]CGTGTCCCAAACCAT | 10580 |
rs539779947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506649 | AGTACTTAGAAAACA[A/G]GAGTTTTCTTAAATA | 10580 |
rs539784643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389575 | TCAAGTTCTAAAGAA[C/T]GCAAAAAAAAAGACC | 10580 |
rs539812643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518425 | GAGATACAATTCTAG[C/T]GTGGAATCTTCTACT | 10580 |
rs539814306 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419432 | AATGGCAGTAGGGAG[A/G]TAAGCAAAAGATCAT | 10580 |
rs539815549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525456 | TTATAGTGAAAAGTC[C/T]CTATTCCACCCCCAA | 10580 |
rs539828393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518223 | GGAGACCAGGAACAT[A/C]CTCATGATCACATAG | 10580 |
rs539832905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367934 | GCTCTCCTACTCCTG[A/G]TCTTTTGCCTTCCAG | 10580 |
rs539839156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474104 | TTTCCTCAGCCCAGA[C/T]ATTTGTTTCTTAAAA | 10580 |
rs539848800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377156 | ATAATCGCAAAAAGA[A/G]AGTTGGGGTGATTTT | 10580 |
rs539859905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321176 | CTAACAAACATCTTT[A/G]TCCCTGATCTATGAA | 10580 |
rs539861831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524880 | GTATACATTGGCATC[A/G]CTAATGACTTGATGA | 10580 |
rs539899922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558631 | CCCTCATCTCCCACA[A/G]CCACTCACTCTGGGG | 10580 |
rs539901659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512801 | GAAGATACATGGGAA[A/G]AAAAAAAAAAGGAAG | 10580 |
rs539902037 | in-del | -/ACAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432313 | AGGGGACCGTAAGAG[-/ACAC]ACACACACACACACA | 10580 |
rs539925128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383001 | GCTTTTAAAAACAGC[C/T]ATTAATTTGTCTGTG | 10580 |
rs539946784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518954 | TCTGGGATGTGTTCA[A/G]CATACACCCAAGACC | 10580 |
rs539963262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518665 | CTCACCCAAACCGGA[A/G]GTTAGCCGGAAACTT | 10580 |
rs539972664 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433767 | CCTGCCTCGTCAGCA[A/C]CTCTTGTATTGAACG | 10580 |
rs539982090 | snp | G/T | 4.95094e-05 | 0.00497517 | missense | SORBS1 | GRCh38.p7 | 10:95384004 | CTGAGCTTGACTTCA[G/T]TGAGGAAGAGCGGGC | 10580 |
rs539989025 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354807 | ATGTCACCTCTCTGA[C/T]AGATGTCAAGAATCT | 10580 |
rs539992299 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490720 | AGGACTTTATTCTCC[C/T]TGGGAAAATATAAGC | 10580 |
rs540014518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553049 | GTGAAACCCCATCTC[C/T]ACCAAAAAACTTTAA | 10580 |
rs540019762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446956 | GACCAGCCTGGACAA[C/T]ATGGTGAAACCCCAT | 10580 |
rs540023156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513835 | ACTGTATTGATTCCA[C/T]GTTCTCATTTTAAGT | 10580 |
rs540023709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505684 | GTGGGGAAATATATT[A/G]TTACTTAATAAACAT | 10580 |
rs540037635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552171 | TTTGGGAGCCCGTGG[C/T]GGGTGGATCACCTGA | 10580 |
rs540039656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397801 | ACAAAGTTGGAATGG[C/T]TGGGCTTTTTTTTTA | 10580 |
rs540042955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444002 | TTGCCTCCCAGGATC[A/G]AAAGTGTTGTTGTGA | 10580 |
rs540056777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406537 | AATCACAACCATGAC[A/G]GTGACCGTCTCCTGA | 10580 |
rs540063839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406669 | TACAGAGGAGGAAAC[A/G]AAAGCCTGGCCTTAG | 10580 |
rs540127965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539385 | TCTAGACACTGCCAA[A/T]TGTCTCCTAGGGGTA | 10580 |
rs540129899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546774 | CAGAGTCTTGCTCTG[C/T]CGCCCAGGCTAGAGT | 10580 |
rs540133867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412625 | GATATGAAAACCTAG[G/T]TCTACACAAATAAAT | 10580 |
rs540147830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412943 | CAGCACTAGAGATTT[C/T]AGAACAGGCCCCAGC | 10580 |
rs540163011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497627 | GCTCACGGTTCAACT[C/T]TCTGGATCCATCATG | 10580 |
rs540177350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506900 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 10580 |
rs540178157 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420013 | ATGCATGACCTAAAG[A/C/G]TTCCTGAAATTTGAA | 10580 |
rs540212128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419913 | TACCAATTCCCTCCT[C/G]TAAGCCAGTGCATAC | 10580 |
rs540213496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392509 | CATCTTTGCTATTAA[A/T]TTTTTTATATCCAAC | 10580 |
rs540223946 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336378 | GTCCTCCCATTCCCT[A/C]TGGGGCCATCTCTTT | 10580 |
rs540225941 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327975 | TTTGGCTTTAATGCT[C/G]TATGATTGCAATGTG | 10580 |
rs540226486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368458 | ATGCAAATGCTTTGA[C/T]ATGCTTGTTTTTAAA | 10580 |
rs540226618 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472941 | GGAGGCTGAGGCGGA[C/G]AATTGCTTGAACCTG | 10580 |
rs540250819 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321578 | TATGTGCTTAAAACA[C/T]AGGAGATATCCAATA | 10580 |
rs540252288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525055 | GAAGAGCTAATGCTA[C/T]AGATGCCAGAATCAA | 10580 |
rs540333821 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335695 | CCAAGTCACTAGACT[A/G]TAAGAGGTGGAGCTG | 10580 |
rs540336964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534394 | AGCACGAGCCACCGC[A/G]CCCGGCCCATGCAGC | 10580 |
rs540356000 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441211 | CACCACACAATGCAA[C/T]TGATGAATGGCAGGT | 10580 |
rs540360662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398844 | TTATAACATCCAACA[A/C]CCACTTTGGGAAAAG | 10580 |
rs540360908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376469 | AGCACACCAAACATT[C/T]AGCCATCTATGCCAG | 10580 |
rs540368922 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373177 | AGGTGTGTTCACCAC[C/T]GACAGCAACAGGTCA | 10580 |
rs540388635 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498881 | GGACTACATACACAT[A/G]TGCACACACACAAAT | 10580 |
rs540393857 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470266 | AGCATTCCAAGTGGA[A/G]ACAATGGTTCCTATT | 10580 |
rs540403500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506047 | TTAACATGTTGATTT[A/G]TTGCTGCCAATCTCT | 10580 |
rs540416672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362898 | GCCTCATAAAGCTTA[C/T]ATTCACCATTCAAAA | 10580 |
rs540425956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447152 | TCTCAAAAACAAAAA[A/C]AAACAAACAAAAAAA | 10580 |
rs540441267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520616 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 10580 |
rs540443645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462992 | TTAAGTGGTGGAATT[C/G]TGATGTATAACCCAA | 10580 |
rs540444531 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552499 | GAGAAGATCCCAAAA[A/C]CTTTCAGTGAGAAAT | 10580 |
rs540471878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370764 | GCAGACTCAGTTTCA[A/T]ACACTTTTTTTGTGT | 10580 |
rs540477193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435198 | GCTACTTCCCCCATA[C/G]CATAACTTCCGGGGT | 10580 |
rs540481854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476427 | CAACCTGGTTCTTCC[C/T]GGGCTTTCCTGATAG | 10580 |
rs540511765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561232 | GCGCGGAACAAAGGC[A/G]CCGCCCGCGGGGGCC | 10580 |
rs540513103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461304 | AAATCAGTCAGCTTT[A/G]CTCTCAAACTTTCAT | 10580 |
rs540514787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527040 | CATACGTTTGAATGA[C/T]GAAATGAATCATGGG | 10580 |
rs540522180 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499866 | AAAATCAAACCACTG[C/G]AAAAGAACACAGCTT | 10580 |
rs540540855 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497997 | TGACTCTTTGCATAA[C/G/T]GTTAATACTCAGTAC | 10580 |
rs540546373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329609 | TAAACGCCCTCTATT[C/T]AGAGATTTCCCTTCT | 10580 |
rs540546701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337706 | GACCCGGAACCATAC[A/G]GGGAAAGGTGGCCCC | 10580 |
rs540549645 | snp | C/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443026 | AAGTCTTGTACATAC[C/G]TCGACTAATAAGGTC | 10580 |
rs540560029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362592 | TTGCTCCTTAAGCCT[A/T]ATCAGTCACCAAGTC | 10580 |
rs540563502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454911 | GCACATGCTGACAAA[A/T]GCACCAAATAGCCCA | 10580 |
rs540573070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560521 | TCTTGAATGGCGCTA[C/T]CACGTATCAAGGAAG | 10580 |
rs540576403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461932 | GATGTTTAGGAAAGC[A/G]AAGAATTGAAATGCA | 10580 |
rs540577172 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377845 | GGGAATGGTTAGGCT[-/T]TTTTTTTTTTTTTCT | 10580 |
rs540583959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429296 | CTCCCGAGTAGCTGG[A/G]ATTACAGGCGTGCAA | 10580 |
rs540590577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533803 | GGCCACATGACTGGC[C/T]GTCCCGCTCTCCCGG | 10580 |
rs540612155 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518771 | AATGAATCAAAGATA[A/G]GTAATAAGGGAAAGG | 10580 |
rs540637543 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428114 | GCCAAATGCTTGACA[G/T]GAAAGAGCTCATTTA | 10580 |
rs540677078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449594 | AAGCCCATGCCCAAA[C/T]TCCACTACCAATATC | 10580 |
rs540677426 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355500 | CCATGATTAATTGCC[A/G]AGCAAAACAAACAGA | 10580 |
rs540695238 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475865 | CAAATGAAGAAAATG[A/G]GGCTCAGAGAGGTAA | 10580 |
rs540695604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554974 | GCAACCTCTACCTTC[C/T]GGGTTCAAGTGACTC | 10580 |
rs540703066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463991 | CCTGTTTCTTCTCTC[C/T]GTCTGTGCCTTCATC | 10580 |
rs540704541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484288 | GGATAAGATTTTAAA[C/T]GAACAGTAAGTCAGG | 10580 |
rs540704854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456055 | TTTAGAACATAGCAC[A/G]GAACACACACAGAAT | 10580 |
rs540754553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357860 | AAATAAAGATAAGAA[A/T]AGGAGTTAGTGCTTT | 10580 |
rs540768604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456830 | GCTGTGAAAACTCCA[C/T]AGAAGCCTTGCTGGC | 10580 |
rs540775304 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429286 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10580 |
rs540779093 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386555 | GCAGAAGAATTGCTT[A/G]AACCCCAGAGGCAGA | 10580 |
rs540786504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316324 | TAGGCGTGGTGATGC[A/G]GGCCTGTAGTCCCAG | 10580 |
rs540788916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500564 | TTTTTTATGCAATTA[C/T]ATATGGAAATGATAA | 10580 |
rs540801755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322996 | AAATGCAAATGTAGA[A/G]TTAGAAGCAAGCATC | 10580 |
rs540841647 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416467 | CACATGCTACATCAA[G/T]TGTGACACCAATCCT | 10580 |
rs540873981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428861 | TTAGCTATCTGCAAA[A/G]GCATTGGGAGTAGGA | 10580 |
rs540878382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447768 | GTCGCTGATACTTCC[A/G]TTCAAGGGGAAGAAA | 10580 |
rs540899455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478194 | GTTGTTTCCACCTCC[A/G]CCAACTATGAGAATG | 10580 |
rs540904953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470603 | AGTTCATGCTTTCCT[C/T]GGAAAGTGGGGAGCA | 10580 |
rs540929032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521368 | GTCAGCCCTAAGTCA[A/T]CCTTTTTCATCTTAA | 10580 |
rs540935051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514712 | CTAATCAGACAGCCA[C/T]ACAAGGCAAAAGAAA | 10580 |
rs540958228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394317 | CTCAGGTACAAAGCC[C/T]TGGGTAGTTGGGTAA | 10580 |
rs540959312 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324447 | GCAGGACTAACTTCC[A/G]TTGCAGGCATCATTT | 10580 |
rs540963909 | snp | C/G | 0.00444689 | 0.0469433 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415758 | GGAGTGCCTTCGGCA[C/G]GGTCACGTGCAACAC | 10580 |
rs540974748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528894 | ACTGCACTCCAGCCT[A/G]GACGACAGAGCAAGA | 10580 |
rs540976134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317220 | AAGGTAAAGCCACTT[A/G]TACAGGGAGAAACTG | 10580 |
rs540994162 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482363 | AACAATATAACCCAG[A/G]ATTGTAAAATCCAAG | 10580 |
rs541007922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516151 | CCAGATCTGGGTAGT[A/G]TAGTTCTTCAGGTGT | 10580 |
rs541010692 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508484 | GCATCTATTACCTCA[C/T]TTTATACCACTTATG | 10580 |
rs541011371 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379901 | AAAGGATGAATTCAA[A/C]TACTGTGAAGGGCAG | 10580 |
rs541019427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464706 | TTGCAGAATGGCCAA[A/C]AAACATGTTTTCTTG | 10580 |
rs541036688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479172 | CAAGCAGAGAATATA[A/G]CAAATCAAAATACTT | 10580 |
rs541046908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385617 | TCCTTCTTGTCCCCT[C/T]TTTTCCCCATTTTTA | 10580 |
rs541066357 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507738 | AACATGGCGAAACCC[C/T]ATCTCTACTAAAAAT | 10580 |
rs541073618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515274 | CACTGACCTTGGTGG[A/G]GGGTGGGTGTGGATG | 10580 |
rs541080311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501281 | CCAATATCGGCAAGA[C/T]TCCCTGGGGACCTCC | 10580 |
rs541107827 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380508 | CAAGGTTACCTTCTA[C/T]GTTTCTTACGTACAG | 10580 |
rs541109471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522598 | TGCATGGCCACTTAG[A/G]GGACACACAAGAGCC | 10580 |
rs541111883 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555006 | CCTGCCTAAGCCTCC[C/T]GAGTAGCTGGGACTA | 10580 |
rs541115468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549050 | TTTTCTGTGCCTCAG[C/T]TGCCTCCACCATGAA | 10580 |
rs541120981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541867 | TCCCTCCACAAGGAG[G/T]CCTCCCATGACCCCC | 10580 |
rs541127078 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482927 | CAAGAAGCCAAAAAT[C/G]AAAAAGGTTGAAATT | 10580 |
rs541127124 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508934 | GAGTTATTCACCAGC[A/G]TGGAGGAAGCAGGAT | 10580 |
rs541128876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407522 | TACTCCAGAGGCTGA[A/G]GCATGAGAATTACTT | 10580 |
rs541133487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415308 | AGAGACAGACAAAGA[C/G]AGTACTGTGCTGAAA | 10580 |
rs541135915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324368 | CAGCTGCTCTTTCCG[C/T]TCCACCAGACCACCC | 10580 |
rs541144841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516594 | ATAGATTACCCCTAC[C/T]CAGAGCCCACTCATT | 10580 |
rs541146925 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512151 | AGCCAGGCGTGGTGG[C/G]TCACGCTCGTAATCG | 10580 |
rs541147864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364497 | TCGCTCTGTCACTCA[A/G]ACTGGAGTACAGTGG | 10580 |
rs541153860 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456858 | GGCAGCAATCATAGG[C/T]GACAGTTTCTACATT | 10580 |
rs541173730 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509967 | ACTAAATGCATGCAT[C/T]TCCAAACTTAAGCTA | 10580 |
rs541174720 | in-del | -/GTGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365215 | TGTGTGTGTGTGTGT[-/GTGT]TTTGTCCCAAAACTA | 10580 |
rs541179149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424130 | ATGAGGTGAGGCCCA[A/C]GAATCTGCATTTCTA | 10580 |
rs541201093 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378438 | CATAATATTCAGTTA[C/T]TGTACCCATATTATC | 10580 |
rs541208787 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403751 | ATTTTTAGTAGAGAC[A/C/G]GGTTTTCACCATGTT | 10580 |
rs541210212 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319138 | ATAAAACATTTGTTT[C/T]TTAAAAAAAGTGTGT | 10580 |
rs541228238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543437 | AAAAAACAAACAAAC[A/T]AAAAAACCCTTTCAT | 10580 |
rs541234836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386834 | GCTCCTTTCTTGGAC[A/G]GGCCTGGTGGCTCAC | 10580 |
rs541256305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502556 | CATTCTACTGCCTCA[C/G]CATCCTCTGTTCTAT | 10580 |
rs541261793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535531 | GTTAAGAGGCAAAAG[A/C]AATATATATATATTA | 10580 |
rs541266292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444768 | TGAATGGAGATGTCT[C/T]GTGAACCAAACAAAA | 10580 |
rs541284803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549833 | TGAATATATGACTAC[C/T]ATCTGTTTGGGAGAA | 10580 |
rs541289241 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450103 | TTATATTAGTCCAAA[A/C]ATTTTTTAAAACTAA | 10580 |
rs541320358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401211 | CATAGCGAGACCCCA[A/T]CGCTACAAAAAATTA | 10580 |
rs541346891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443446 | GCCTGGGTGACAGAG[C/T]GAGACTCCAACTCCA | 10580 |
rs541358103 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353402 | TTACAAATAATAACT[A/G]TACATCAAATGCTTC | 10580 |
rs541395745 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325087 | ACTGCTGGTTCACAG[A/T]CCAACTGTAGGCGGC | 10580 |
rs541397789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332804 | GCCTTCCATACATTA[A/G]GTATCACGGTCCCGC | 10580 |
rs541431306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465176 | TTCTGAATTTTAACA[C/T]GGTGCCTTGGATGAA | 10580 |
rs541453816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417127 | GCTCACACAGCATCC[C/G]TCTCTTCTCAACACT | 10580 |
rs541457545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537099 | TCCCTCCTCCTGCCT[C/T]CACCCATCCCCATCC | 10580 |
rs541475005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389812 | ACAGGCCAGTCAATG[C/T]CTTTTGCACTTGCTA | 10580 |
rs541483782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325700 | GGGATTACAGGCGTG[C/G]GCCACCATGTCCAGC | 10580 |
rs541493005 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346023 | TTCCACAGAAAAGAT[A/G]GGTCAGATCAAGCCA | 10580 |
rs541533808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531045 | AGCTCGCAGCCAGGT[A/G]GAGCAGCACTAAACT | 10580 |
rs541535272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535576 | GTATGTATCTGCATA[C/T]AGAAATCTTGGAAGG | 10580 |
rs541553204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430999 | TCATCCACCAGCATG[C/T]GCCCTGGCACCTGTT | 10580 |
rs541561305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332112 | CTCTCTCACTGAGTG[A/C]CCTGCTGCACCCTTT | 10580 |
rs541561598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471896 | AAAGCTCCATGAGGT[A/G]GAACAATTTGTAAAT | 10580 |
rs541598248 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373443 | CTATTCTAACAACTT[G/T]TTGGAGCTAAAAAGG | 10580 |
rs541648776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451700 | TAAACACAAGCCCAG[A/G]ACACAGAGCCATTTT | 10580 |
rs541664848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556984 | AAGAGGTAAGAAAAA[G/T]AAATGGATAGTGGAG | 10580 |
rs541671835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432246 | CATCTGCAGCATGTG[A/T]CTGTCAGTTTGAGGC | 10580 |
rs541673788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425562 | ACCATGGAAAAAAAT[A/G]AGCATTGTTGATCTC | 10580 |
rs541676921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365735 | AACCCCACAGTGAAT[A/G]CAAGAGACTTTACAC | 10580 |
rs541703688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558336 | CCAGATACATCTGGA[A/C]ACAAGATCTACAATC | 10580 |
rs541711375 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403496 | ACTCAGAGAAAGCGA[C/T]AGCATCAGTCTTATT | 10580 |
rs541736637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426252 | TGACAGGTGTTAATA[C/G]TAAGTCTAAGGGTGT | 10580 |
rs541739013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359676 | TGTTACTCACCATGA[A/G]TACACCCCTAAGATA | 10580 |
rs541740681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326597 | GTTTTTTTCAGGGGA[C/T]GGAGACATGGCATGG | 10580 |
rs541742144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550935 | AGCAGAGCAGGAGCC[A/T]CTAAACAAGTGCCCA | 10580 |
rs541769181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557882 | TAATCTGTCCCCAGC[C/T]TCCTACTTTCTCGTC | 10580 |
rs541789795 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385320 | CTTTCCCATTTCTAA[-/C]ATCTTGCTAATCTGG | 10580 |
rs541801623 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527578 | CAAAGCAACTATACA[A/C]CCCAAGACAATGTAT | 10580 |
rs541801872 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433989 | AGTTACTTCTGAAAG[C/T]GCCATTGGATAAAGT | 10580 |
rs541811083 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449391 | ATAAGCACGTGCCAC[C/T]TTGACTACTTTTTGT | 10580 |
rs541812675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517735 | CACAGCTGACTGCAC[A/G]TATGTGCAGATAACA | 10580 |
rs541827916 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313544 | TGGAAAATATTCCAA[G/T]TATTTCCAGCTATGA | 10580 |
rs541862239 | snp | C/T | 1.69804e-05 | 0.00291374 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381841 | TATTTTCATGACAAC[C/T]GGCATTAGCTTCCGA | 10580 |
rs541896133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453052 | GCACTATGAGAGGCC[A/G]AGGCAGGCGGATTAC | 10580 |
rs541898136 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460525 | GCGACCAGCCTGGGC[A/C]ACATGGTGAAACCCC | 10580 |
rs541898701 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504136 | CAATCCTAGTGAAGT[C/T]CAGAGTTCATTCTCC | 10580 |
rs541904324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321233 | TTATCTCCCTAAAAC[A/G]AAATATGATCAATAT | 10580 |
rs541908381 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444377 | GCAGGGATTATAGGT[A/G]TGAGCTACTGCACCT | 10580 |
rs541924246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368028 | GTCACAGGTCACTGG[G/T]CAATGGCCCACCGTG | 10580 |
rs541924346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497728 | CCACCCCTTAAATCA[C/T]CCCTCACCATCACCA | 10580 |
rs541944733 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552915 | AAAAAAAAACAGTAA[C/T]AAAATAAAAAGGAAC | 10580 |
rs541959644 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453508 | ACGCCTGGCTAGTTT[C/T]TGTATTTTTAGTAGA | 10580 |
rs541963736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355338 | GGGGTATGTTGGGGA[C/T]TGGTGCAAACAGCAA | 10580 |
rs542013182 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497587 | ATCTCCAATACCCCA[C/T]TTCGCCCTCCATCAC | 10580 |
rs542013208 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367440 | AATACAAATCATCAC[A/C]AAATTAATTTGGAAG | 10580 |
rs542018311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391852 | ACTAGAATTTAGACA[A/G]AGATGGCAGCCCTTA | 10580 |
rs542022536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481926 | TGGTCCCTCCTTTGC[C/T]CCTACACACACAGCC | 10580 |
rs542024850 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456403 | GTGGGTTAGTTACTG[C/T]CAGAGTGGGCTCCTC | 10580 |
rs542052797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343420 | GCCTCCCCAGTAGCT[A/G]GGATTACAGACATGC | 10580 |
rs542053861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524471 | GCCGCCATTGTGCTC[C/T]GTGCATATGCTCTCA | 10580 |
rs542055932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411716 | ACCCACAAGATGAGG[A/G]CCACCCCCTCACTCA | 10580 |
rs542088505 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545022 | ACCACGTCCAACATA[A/G]AGGCCCTGCAAAGCA | 10580 |
rs542089666 | snp | C/T | 1.72169e-05 | 0.00293396 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336562 | TCCTCCCCGCCTGCT[C/T]GCCACCTCTATGCCG | 10580 |
rs542101573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504353 | TGCAAGAGGACGGGG[A/G]AGGACTCTGCAAAAG | 10580 |
rs542122346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447047 | TCTGGAGGCAGAGGC[A/G]GGAGAATCACTTGAA | 10580 |
rs542124034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382393 | CAATAAATGTCAGTT[G/T]CTACCATAATTGCAT | 10580 |
rs542125051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350610 | TTTCCTAACTGCAAA[A/C]GTCTTTGGGCTTCAA | 10580 |
rs542156060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466312 | TGGCTGTAGTGGCAG[C/G]CGCCTGTAATCCCAG | 10580 |
rs542160926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511554 | CCTATGTTGCTGCCT[C/T]GTTTCTTGCTTGTTT | 10580 |
rs542168467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545523 | CCCTGCCTCTATTAA[A/T]AACAAAAAAAGTAGC | 10580 |
rs542173865 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374329 | GGAAAAAATTCCACC[A/T]TTTTTCCTGAAAGCT | 10580 |
rs542185346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375421 | CCATTTCAAACTTTG[G/T]GAAATATCCTACATC | 10580 |
rs542207312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446583 | GCCAGCATGCTCCAG[A/C]TTCTCCTATGCACTA | 10580 |
rs542219319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405285 | CTCTACAAAAAAACT[C/T]TAAAAAAAAAACTAG | 10580 |
rs542235781 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505012 | AGCTGCCGTCGTGTA[C/T]AGGATACCAAGTGGT | 10580 |
rs542259196 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550888 | TGCAGTAGCTGATTT[A/C]GGTTTCCGCATTGTC | 10580 |
rs542271939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462094 | CTAATAGTCCATTAA[C/T]ACTTTATCCTATCAC | 10580 |
rs542275911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360963 | GGACTACAGGCATGC[A/G]CCACCACACCCGGCT | 10580 |
rs542276168 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430014 | ACTATCCCTTAATTC[-/TT]TTCCGAGTACAGTAT | 10580 |
rs542292271 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312732 | GCAAATGTGGCTTTA[C/G]AAATTGGTTTTATTT | 10580 |
rs542297924 | snp | A/G | 0.000115629 | 0.0076027 | missense | SORBS1 | GRCh38.p7 | 10:95399180 | CCCACTCTTCTTTCT[A/G]AGACAGGATCTGGAA | 10580 |
rs542298632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414096 | TCCCCGAGATCTCCC[C/T]GCTCCCTGGTAAGTA | 10580 |
rs542299529 | snp | G/T | 1.78398e-05 | 0.00298657 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377312 | CTTTAATGCTAGTGC[G/T]TCACAAAGCAGCTCT | 10580 |
rs542339077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497268 | GGCATCTTCATCATG[A/G]CATGAAGCGTGGGCA | 10580 |
rs542339803 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471264 | TAATTCACTCATGTA[C/G]AGGCATTTATTCATT | 10580 |
rs542342365 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538710 | AATAACTTAATTTTT[A/T]TAAAAAATAGCACAA | 10580 |
rs542352478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404706 | AACCCACAGAGCGCC[A/G]CCTGGTAACAGGAAT | 10580 |
rs542359032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449361 | CGTGCCTCAGTCTCC[C/T]AAGTAGCTGGGATTA | 10580 |
rs542367713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383409 | TGACAGAGCAAAACT[C/T]CGTCTCAAAAAAAAA | 10580 |
rs542372394 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405962 | GGGAGGCAGGAACTA[C/T]GCCTATTTTCATCAT | 10580 |
rs542385765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398947 | TGATGGGGTTCACAT[A/G]TACTCAGAGTGTACA | 10580 |
rs542407236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468711 | ATCTAGCTCCAAATA[C/T]GAGCTTCTACAAAGC | 10580 |
rs542415632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533015 | TCATGCTTCAAATGT[A/C]CTACACATCCCTTCG | 10580 |
rs542448858 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399744 | TGAGAGGACTTATCA[C/G]GATAACTTATGCCAA | 10580 |
rs542477086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532205 | AACCCTCACTGAGCC[C/T]CACTTCCTCATCTGC | 10580 |
rs542519155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525562 | TGTCCTGTTTTTGCA[C/T]AAATGATAGCATACC | 10580 |
rs542521294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492743 | AAAAGCAAGGAGATG[A/G]GAAGAGCCCCTACAA | 10580 |
rs542522623 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406774 | ATAAGGGGCACAAAT[C/T]GCCCAAGATAACACT | 10580 |
rs542540273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397880 | CACTCCCACTTTACA[A/G]AAGAGGAAATGAGAT | 10580 |
rs542546817 | in-del | -/ACT | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405711 | CCCAAAAAGGAGAGA[-/ACT]TGCCCATATCTCCCA | 10580 |
rs542583221 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488392 | AAAATGGAAACCATA[C/T]TCATTAGCATGTCTT | 10580 |
rs542585109 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533163 | AGTCCCTATTGAATG[C/T]TTCTTTCTGAGAAAC | 10580 |
rs542602020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329345 | GCTTCCCAAGTAGCT[A/G]GAACCACAGGCACTC | 10580 |
rs542602793 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429409 | CAACTGATCTGCCCA[A/C]CTCGGCCTCCCAAAG | 10580 |
rs542617921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385148 | GCCCTTGTGGAAGTG[A/G]CTGTATCTTCTGAAC | 10580 |
rs542621153 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340046 | TAATGATTTAATTAC[C/T]GATCCCCTGCTGTTG | 10580 |
rs542621463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468045 | TGGGATTACAGGCAT[A/G]CACCACCAGGCCCAG | 10580 |
rs542648197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519222 | AATGCAATCAGCAAC[C/G]GGCAGAGCTGGAGCC | 10580 |
rs542652741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337926 | TAAGACAACAGGATG[C/T]GGCTATCACTGTCCA | 10580 |
rs542689475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330296 | TTAAAAACCAAGGCT[A/T]GATGCCAGTCAACAA | 10580 |
rs542689993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323147 | ATATTGGTCCCCTCA[C/T]GCTCAGCTAGTAAGC | 10580 |
rs542691951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526001 | AGGGAAAGATGAGCA[C/G]CATCACCCTCAGATA | 10580 |
rs542720206 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441920 | CCAGATCTTTTATTG[A/C]GTTATAGTTTGCATA | 10580 |
rs542731907 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336998 | GTGTGGGGAAGGTAG[A/G]GCCAGTGGAGAAGCT | 10580 |
rs542745737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317884 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCGCCT | 10580 |
rs542755008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393433 | ACCAATGATGAGAAG[A/G]GCTGAGAGGGATGGT | 10580 |
rs542756676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461364 | TAAGTATCTTAAATT[A/G]AGATAACAAATAATC | 10580 |
rs542757688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428514 | GGCAACTGAAGCCCT[A/G]TAAGGTGGAGTAATT | 10580 |
rs542776961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316010 | TATGGAGAATGGCCA[A/T]GAAGGTTAGAGAACT | 10580 |
rs542783784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435279 | CCCCCATCTGTTAAA[C/T]GGCAGATGGCCTTGC | 10580 |
rs542788183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411980 | ATTTAGTTATGAGGG[A/G]CAGCTCAATGTCATG | 10580 |
rs542790125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559690 | TTTCCCCTCAGGCCA[A/G]GAAAGAGACATCAGA | 10580 |
rs542792654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424013 | GGTAGGGTAAAGGTT[C/T]CAAGTGATTGGCATT | 10580 |
rs542799682 | snp | C/T | 4.97863e-05 | 0.00498906 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357767 | AGGAGCCCCGTCTGA[C/T]TCCCTCTTCACTGCA | 10580 |
rs542806579 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516065 | TGACATCCACACCCA[-/C]CCCCCCACCAAGGTC | 10580 |
rs542825161 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351319 | CTGTGTGGCGTCGAG[C/G]TGCAATATCAGCCTC | 10580 |
rs542825500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457042 | AAAATAAAAGGTGTC[A/G]AAAAATCCTTTAGAA | 10580 |
rs542832774 | snp | A/T | 0 | 0 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415585 | GGAACGAAGCCTGAG[A/T]CCCCAGGGAAGGACT | 10580 |
rs542847311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448702 | AAATATAGTACAATG[C/G]GATAACCCTTCTGCT | 10580 |
rs542863899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553963 | TGGCCTTAAGTGATC[C/T]GCCGGCCTCAGCCTC | 10580 |
rs542868635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422294 | CAGGAAACAAGCATG[A/G]AACTGCATAGAAGGT | 10580 |
rs542870276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429817 | ACTCCTGTTGCAACA[C/T]ACTGCCTTTTGCCCT | 10580 |
rs542890931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548402 | ATAGTAACCAGAATT[A/T]ACTGAATTATTACTA | 10580 |
rs542897756 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485672 | ACGAGCAGTAATCAC[C/T]GGAGATGATGCTGAT | 10580 |
rs542909894 | snp | A/G | 7.23524e-05 | 0.00601423 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414573 | GGGACCAGCGGAGGT[A/G]GTGGTGAGAAGGATG | 10580 |
rs542929897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422927 | TTACAAGCCCGACTG[C/G]AAAGGCAGCTGGGCC | 10580 |
rs542932540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491852 | TCACTCCTGTAGACA[C/T]TTGCAACCCCCAAAG | 10580 |
rs542938619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363601 | ACCACTACTGATTTA[C/T]AGATCTGAAATGCTA | 10580 |
rs542978469 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335595 | CAGGATCATAAGCCC[G/T]TGTAATCAACCACTC | 10580 |
rs542982242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455809 | CATGGTGCCGTATGC[A/G]TGTAATCCCAGCTAC | 10580 |
rs542995334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353302 | TACATGGGAATCTTA[C/T]ATCTTGTGGCAGGAA | 10580 |
rs542996447 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365404 | GCAGCAGGGTTAACA[C/T]GGGCAGTCAGGACTG | 10580 |
rs543000010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435952 | CTTGGGGGAGACTTT[C/T]GTAACCATTTTCAGA | 10580 |
rs543000172 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464083 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 10580 |
rs543011288 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464914 | AGGAAGCAGTCCAGG[C/T]GGAAAAGGAAAAAGT | 10580 |
rs543040547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338853 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10580 |
rs543043729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484372 | GGGGACCACAGCAAA[C/T]TGGACTCCCTCCTGA | 10580 |
rs543066030 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408639 | TAGAATTCCAGAAGT[A/G]GAGTAAAGTTATTCC | 10580 |
rs543099644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317987 | GAGATCACACCACTG[C/T]ACTCTAGCCTGGGCA | 10580 |
rs543121336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358660 | GCCTGCCACTAACAC[A/G]CTGTCATTCACACAC | 10580 |
rs543140442 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536016 | GAAATAAAATCACTG[C/T]TCGTCGCACAGCCCT | 10580 |
rs543147136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484849 | GCATGGTGGCGCACA[A/C]CTGCAGTCCCAGTTA | 10580 |
rs543148122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450303 | CAGAGATGTTTACCA[C/T]AGCTTTATTAGTAAT | 10580 |
rs543149747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344881 | AGGAGCCCTCTCTCC[A/G]GCATTAGCAATGTTG | 10580 |
rs543156849 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403277 | CAGAGAGGGAGGCTG[G/T]CAGCCCTGGAGTCCC | 10580 |
rs543170121 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369040 | CATATACTCTAACTC[C/T]CAAGAACTACTCACC | 10580 |
rs543172232 | in-del | -/TGAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385128 | AACCTATACAAGACC[-/TGAA]TGAAGCCCTTGTGGA | 10580 |
rs543183912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476489 | CACCCTAGAGAGCAA[A/G]GACTAGGTTTTATAC | 10580 |
rs543217917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478370 | GAATCTGAACTGTCA[C/T]TGATGAATCACTATC | 10580 |
rs543222559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413647 | ATTCCCATATTACAA[A/C]TCGCAATGAAGTTAT | 10580 |
rs543234152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315201 | CACGCTGCAGAGATT[C/T]CTGCTCCAAAACCCC | 10580 |
rs543260347 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391962 | AAAAACAAACTTCTC[C/T]CCAGGAGAGAGACTC | 10580 |
rs543278708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444504 | TTTTCTAGCCTTTAG[A/T]TACATAAATAGCAAG | 10580 |
rs543290988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472003 | GCTCTGGTTTGTCTA[A/C]ATCCAACTGGTAGTC | 10580 |
rs543294329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509220 | GAGAGCTCAAGGAAG[A/G]TACCTTCTAGGACCG | 10580 |
rs543311139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437130 | CTGTGAACACATCAC[C/T]GTTTATTACAGGTGA | 10580 |
rs543319875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347128 | CCCTGTTGCTCAAAG[C/T]TGACATCTAGTTTCC | 10580 |
rs543320150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515974 | AGCTGCCTCCACCCT[A/T]CTCCAGACATCACAG | 10580 |
rs543326171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331138 | GAATCTTTTGTTTAC[C/G]GACAGAGTAGCTGCC | 10580 |
rs543326909 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379620 | CAGAGTTAAGCAGAC[A/C/G]TAAGTACCTCAAATG | 10580 |
rs543352245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479360 | TTCCAAGCCATAGGA[C/T]TTCCAAGCTAAAGGG | 10580 |
rs543356014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339618 | TTTTTGACTCATTTA[A/C]TGTGAAACAGATACC | 10580 |
rs543365203 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514609 | TTATCCATAATCATC[A/G]ATAACTGTATGCCCA | 10580 |
rs543389602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371685 | TACTTGCTACGGAGA[A/G]CTACAAAAACCTACC | 10580 |
rs543399285 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388212 | CTCGAACTCCTGACC[A/G]CAGGTGATCCACCCG | 10580 |
rs543420068 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366558 | GGAAGAGGCTGGTGG[A/C]ACCCCACAAAGGAGT | 10580 |
rs543425343 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472307 | CAATACATTTTATGC[C/T]TCTAAAGGGGTTTGA | 10580 |
rs543428356 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538697 | GAGTAGTCAGAGCAA[G/T]AACTTAATTTTTTTA | 10580 |
rs543446681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488077 | AACTTTTGGATGATA[C/T]AACTATTGAATGAGA | 10580 |
rs543447562 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334718 | ATGACTCAACACTGA[C/T]GATAAGGATGTCCCC | 10580 |
rs543467934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495131 | ATCTCGTAATCCACC[C/T]GCCTCGGCCTCCCCA | 10580 |
rs543487586 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485745 | TCTCCAAACCAGGGC[-/A]AAAAAAAAAGAAAAA | 10580 |
rs543493588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373462 | GAGCTAAAAAGGTAT[C/T]TTTTTAGTCAGGATC | 10580 |
rs543502061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543212 | AACCCACATGCCCTC[A/C]TGGCACCCTGTACTT | 10580 |
rs543512508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409368 | TGGCACCGCTGAAGG[A/C]GAATGGGCTCCTGCA | 10580 |
rs543556607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365896 | AAATTAACATGATGG[A/T]TCTAGCTAGAGCTTT | 10580 |
rs543556821 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554352 | AGCCACCACACCCAG[A/C]CTATTTGTCTTTCAA | 10580 |
rs543572342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333456 | CATAAAACTATGATC[A/G]AATAAATCTGTATGC | 10580 |
rs543572790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502271 | GCAAATTTCCTTTCT[A/T]TTTATGGAAAAAATA | 10580 |
rs543581428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396134 | CGGCACAGGCAGCGA[C/T]GGGAGCCGGTGGGGT | 10580 |
rs543582833 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462069 | TTTTTAATTAGACAG[C/G]CTTTGATCTCTAATA | 10580 |
rs543602766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537365 | AAGACACACAGTGAC[A/G]TGCTGGAGAAGCCAC | 10580 |
rs543617265 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356077 | GGATGGTGGTGAAGC[A/G]GGTGTATGAGGCCGG | 10580 |
rs543624398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404439 | CAGTGATTCTGAACC[C/T]TGAAATTCATGAGTG | 10580 |
rs543634788 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355123 | GGAAAAAAAAATTCC[A/C]CCCCCCACCCCATTT | 10580 |
rs543636390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332878 | GGGCTGAGAGAGGCT[C/T]ACACAGACCATTGCA | 10580 |
rs543640168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396578 | GCAATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 10580 |
rs543667831 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411631 | GGCTTTAAGAACAAG[A/G/T]TTTTAAATAGTTACT | 10580 |
rs543668021 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528983 | AAATGAGAACCCACA[A/C]AGCAGCTATTAAAAC | 10580 |
rs543695573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507438 | ATATTTTCCTCCTGG[A/G]AGATATCAATTAATA | 10580 |
rs543733054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496362 | GGCCATAACTGGTGC[C/T]AACATCTCTAGGACC | 10580 |
rs543761384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390936 | ACAGGCATGAGCCAC[C/T]GTGCTGGGTCCCTAA | 10580 |
rs543767804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411553 | AGACAGTTTCCTTCA[C/T]GATATCTATACATTT | 10580 |
rs543779316 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358277 | CCTGGATTATTTTTC[A/T]TGGTTATTCTTCGTA | 10580 |
rs543792982 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535639 | TCTGTTGGATAATAT[A/G]TAATTCATCACCTAA | 10580 |
rs543793767 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360820 | CAGCTTTGGCCAGAA[C/T]TTTTTTTTTTTGAGA | 10580 |
rs543799145 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319402 | GGTCTGTGCTGTTTT[C/G]TCTGTTCTAGCAGCC | 10580 |
rs543808807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459330 | AACTAACCAGCAAGC[C/T]CAAATGCAGAGAATC | 10580 |
rs543850082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426919 | TCCCTCCAACTTCTC[A/G]GTTGGCCCTAATTCT | 10580 |
rs543870546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489618 | GCCTTGGCACAGAGC[A/G]GGCATTAATACATAT | 10580 |
rs543889058 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383232 | CCAGCCTAGCCAACA[C/T]GGCGAAACCCTGTCT | 10580 |
rs543892244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424847 | ACCCCATACTCCTCA[C/T]AGGGAGTATGATTCT | 10580 |
rs543896017 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430295 | GAAACTTTGTCTCTA[C/T]AAAAAATACAAAAAT | 10580 |
rs543898328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390111 | AAGCACTGAGACAGA[C/T]CATTTTGACACCACA | 10580 |
rs543903839 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524937 | ATGACGCAGGGTTCA[A/T]TTCTTAGGCACACAC | 10580 |
rs543909965 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510769 | GGAATTTGAGACCAG[C/G]CTGGACAACACAGTG | 10580 |
rs543913733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557596 | TGGATCTAAAGGCCT[C/T]AGTTGGTCCTGAAAC | 10580 |
rs543914061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550393 | AAACCAAGGCCCAGA[C/T]AGGTTAAGGGACTTC | 10580 |
rs543926836 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515702 | CCCCAGAATTAATGC[A/G]GCTGCTCCCTTTACT | 10580 |
rs543931703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429239 | TGATCTCACTCACTG[A/C]AACTTTCACCTCCCG | 10580 |
rs543943321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465650 | GAAATATACTGGTAA[A/G]TTAGCAAGTCCAATT | 10580 |
rs543954580 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321395 | GAACCATATGCTGCA[G/T]CTACACGGGCCCTTT | 10580 |
rs543955044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325835 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 10580 |
rs543978852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518856 | TGAAAAAATACCATA[C/T]GCTGCAAAAGAAGCA | 10580 |
rs544002034 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463872 | ACCAAGGTGAGAGAA[C/T]CATCAGGAAATGGGT | 10580 |
rs544002601 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467816 | TTAAGAGAAACTGAG[C/G]ATTCATATACTCTGA | 10580 |
rs544019033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481651 | CAATGCAGGCTGTTG[C/T]CCATGCATGTGACTG | 10580 |
rs544041178 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313782 | GCAGGGAATGGGTCA[C/T]TTCTGTATTTGTCTC | 10580 |
rs544048143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550799 | TAAAAGGACAGTAGA[C/T]GGATGCATTTCTTAA | 10580 |
rs544049458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322250 | ATGTAACATTCCAGA[C/T]GAAGCACATAAGTCC | 10580 |
rs544062037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489059 | TCTCACCTACTGCTC[C/T]TATTTCACATCACTC | 10580 |
rs544084528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537972 | AAAAAAATTAGCCAA[C/G]CATGGTGGCTCACAC | 10580 |
rs544085891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461217 | AAAATTAATTTTATT[A/G]CACAAATTGAAGACA | 10580 |
rs544107684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419755 | TTTTTGTTGTAAACA[C/T]TGTAGGAACCACACA | 10580 |
rs544136970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354735 | GCATGATTGAGCCTA[C/T]GTCATATGAAAAAAT | 10580 |
rs544137821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551760 | ACTGTACCCATGAAA[C/T]AAGAATAGAATGTCA | 10580 |
rs544137846 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440842 | TGTATACTAAAAATA[C/T]CTGTGGTTTATAGTA | 10580 |
rs544150298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546897 | GCGTGCCACCACACC[C/T]GCAAATTTTTTAAAT | 10580 |
rs544165345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376395 | AATAATTTTCAGTAA[C/T]GTGGAAGAAAAGAAA | 10580 |
rs544165674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452595 | GATAAAACCACTAAA[A/G]CATTCAACATAATAT | 10580 |
rs544187482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334650 | CCTTACTCGGAGATC[C/T]GGCACCGTGCGCACT | 10580 |
rs544201528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481022 | AGTAGGGCATGTGGG[A/G]TGGGAGGAGTGCTAA | 10580 |
rs544207843 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419375 | TCTAGAAACAAAACA[C/T]GTGGGCTAGCACGCA | 10580 |
rs544212881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546399 | TGCTGGCATCTGCTC[G/T]GCTTCTAGGGAGGCC | 10580 |
rs544248086 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525134 | GATTGTGCAAAAGTA[C/T]GGGCTGGGGGCAGGT | 10580 |
rs544259133 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350667 | AGCACTGCTGAACAC[G/T]TCACACAATTCATCC | 10580 |
rs544266935 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522614 | GGACACACAAGAGCC[A/G]ATTTCCAAGGCTGGC | 10580 |
rs544304671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474315 | TGCCACCAAAGAAAC[A/G]GAGTCTCTCGTGTCC | 10580 |
rs544346756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491583 | TCAGGTGGTGCTAAG[A/C]ATTAAAAGCAGTCAC | 10580 |
rs544362211 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493108 | CCCGCCTGACCAACA[C/T]GGTGAAACCCCATCT | 10580 |
rs544364182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412349 | GACTTTTATTCTTCC[C/T]TCTTTCTCTCAACTA | 10580 |
rs544367694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540360 | TATAGTGGCATGGCT[A/G]TTTGTTGCCATTGGA | 10580 |
rs544380759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512209 | GATTACTTGAGATCA[A/G]GAGTTCGAGACCAGC | 10580 |
rs544386305 | snp | A/G | 1.65474e-05 | 0.00287636 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406081 | ACGGTTTCAACAGGA[A/G]CAGGGATTAACACAT | 10580 |
rs544403574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453653 | CATTAAGTTGTTCTT[A/C]AGATTAAATTTTAAA | 10580 |
rs544420358 | snp | C/T | 0.000121249 | 0.00778523 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356456 | CATGGAACGGGACCG[C/T]TGAATCAGCTGCTCA | 10580 |
rs544428303 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446736 | CCTCTGTTTAACCTT[C/T]GGAACCTAACTTCAG | 10580 |
rs544429309 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519241 | AGAGCTGGAGCCAAG[G/T]CGCCTGGTGCTGGCC | 10580 |
rs544437356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384676 | CACCAGCTCAGTGTA[C/T]GGTTAAGCTCACCGA | 10580 |
rs544465265 | snp | C/T | 6.59761e-05 | 0.00574314 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441121 | ATGAGTTTAAAATGA[C/T]TTACCAGAACTCATG | 10580 |
rs544470771 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505854 | CCTAAGCTCCAATCT[C/G/T]TCATCCCTCCTGTAT | 10580 |
rs544492082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521482 | GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC | 10580 |
rs544503742 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493738 | TTCCCTGAATCAGTA[A/C]CTAGTGGGCAGGTTC | 10580 |
rs544506339 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319287 | CTTTTAAATGTGGAT[A/G]TCATTTTTCTGAAAC | 10580 |
rs544506891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533757 | CTCTGTTCTTGTGGA[A/C]CTCAGCACACAGCAC | 10580 |
rs544563288 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362212 | TCCAATTGTGCTAAC[A/G]GGCAGGTTCCGGAGG | 10580 |
rs544565241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368141 | AGAGCCCTTCATGCA[C/T]CCCAAATGCCACATC | 10580 |
rs544587386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397998 | GGTTTGGGAGTCAGA[C/T]AGACCATTCTGTCAC | 10580 |
rs544598645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434380 | ACTGACCCTTCTCCT[A/C]AAGAAAAGAGGGGCA | 10580 |
rs544607821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497840 | TTAATCTCTTTGTTT[A/C]CCCCAAATGACTGCC | 10580 |
rs544614533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363819 | CAATTTATTAAAGTG[A/G]ACTTAAAACAACACC | 10580 |
rs544614895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320614 | CGATCTCTTGTCCTC[A/G]TGATCCGCCCACCTT | 10580 |
rs544622501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469571 | ATCTGAAAAGTCTTG[C/T]CCAAAAGAATCCTAT | 10580 |
rs544646450 | snp | G/T | 0.000752615 | 0.019384 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355927 | AAGGTTGTCTGGGGT[G/T]GTGGTGGAGGGGCTT | 10580 |
rs544648920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398728 | GAACACTCACATACT[C/G]AAAGCCTCTGAAAAG | 10580 |
rs544666058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514568 | ACAGTGGTCACTCCA[C/T]CCCAGAAACATCACG | 10580 |
rs544678604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560398 | GAGAAAGCATGCACT[A/G]GTGAATTTCAAAGCC | 10580 |
rs544688309 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424527 | GTAACAACTATTTAC[A/G]TAGCACTTATATTAG | 10580 |
rs544754020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370698 | TCTTACTCTCTCTCG[C/T]ATACCCTTTAATAAA | 10580 |
rs544758086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393600 | GGCAAGGTTTTCTGT[G/T]GCGTTCTGGACACAC | 10580 |
rs544762634 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488804 | TATCCTGAGCCTGAC[C/T]GCTTCTTCGTATCAT | 10580 |
rs544799315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507709 | CTGAGATCAGAAGTT[C/T]GAGCAGCCTGGCCAA | 10580 |
rs544800730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500517 | TTTTGAAGACTCAGA[A/C]TTTTAAAAAAGAATG | 10580 |
rs544814600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553997 | AACTGCTACGATTAC[A/G]GGAATGAGCCACTGC | 10580 |
rs544881191 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453386 | TCTGTTGCCCAGGCT[-/G]GAGTATAATGGCACG | 10580 |
rs544897947 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490965 | CAGCATAGTTCTCTG[C/T]AAATCGCATTCTACA | 10580 |
rs544917189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392424 | AGTGGGGGCGTGAGA[C/T]GGAATTTACCCTATT | 10580 |
rs544922803 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364522 | CAGTGGTGCGATCTT[G/T]GCTCACTGCAACCTC | 10580 |
rs544922972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526933 | TTCTTTCCACTGTAC[C/T]AACACCAGGCTCTAA | 10580 |
rs544936845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493329 | AAAGAAATACTAAGC[C/G]TTTCATGATGGACAA | 10580 |
rs544940743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323925 | CCACAGTGAGCATGA[C/T]TGCACCGCTGCACTC | 10580 |
rs544946126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484985 | TCTCAAATAGAAAGG[A/G]AACAAAAAGTGTAAA | 10580 |
rs544948190 | snp | A/G | 9.33977e-05 | 0.00683302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357827 | AGGTAATTTTGAAAG[A/G]AAGAGAGAAAAGGGA | 10580 |
rs544958940 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467348 | GCAGTTAGGGGCAGG[C/G]AGCCGGCCCAGCTTC | 10580 |
rs544966700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535340 | AATCTGCCTTCACTT[C/T]CTATAGCCTACCATC | 10580 |
rs544973841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521531 | TCAAGGGATTCTCCT[A/G]CCTCAGCCTCCCGAG | 10580 |
rs544974278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315292 | TATCTCACTTAGGCT[C/G]CCAAATAATGCTGGG | 10580 |
rs544987913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423167 | GTCTCTACTCTCTGT[A/C]CTTGATCTAACCCAG | 10580 |
rs544990621 | snp | A/G | 3.48955e-05 | 0.0041769 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414605 | TGGCGTCTGGCTAAT[A/G]GGGGCAAAGGAGCCA | 10580 |
rs545036089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514107 | TTGAACATTGACTAT[A/T]ATGTAGAAAAAAAGA | 10580 |
rs545062255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316191 | GGCATGGTGGCTCAC[A/G]CCTGCAATCTCAGCA | 10580 |
rs545070322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462232 | TTTCTTAAAGAAAAC[A/C]ATTGGAAAAGCAATT | 10580 |
rs545093049 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555031 | GGACTACAGGCATGC[A/G]CCACCACGCCCGGCT | 10580 |
rs545096391 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354000 | AGAGTTGTGCACACA[C/T]GCACACCCTCCCCCA | 10580 |
rs545102694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324494 | TTGGGAAGCCTCCTC[A/G]AGTTCTCCAAAAACC | 10580 |
rs545107872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522313 | TACTTAACATATGCA[C/T]GTTTCCCAGTTTAAC | 10580 |
rs545130897 | snp | A/C | 0.000399281 | 0.0141238 | missense | SORBS1 | GRCh38.p7 | 10:95422004 | TGCACACTTCTGTAG[A/C]CCTTGGCAGCGAGTG | 10580 |
rs545168828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416999 | TTTCTCAAAATCTAG[C/G]CCCATGCCCATCTCA | 10580 |
rs545169691 | snp | C/G | | | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415930 | AGCGCTGCTGGGGTT[C/G]GGATGAAGCACTGGG | 10580 |
rs545179614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541741 | CCCTCTTGCGGGGAT[C/T]ATCTCCTCTCTAATC | 10580 |
rs545189979 | snp | A/C | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312355 | ACAGTCCCACTTCTT[A/C]AGCACATTATTTTTT | 10580 |
rs545194952 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364707 | TCCCCCAACCTTGGC[C/T]TCCCAAAGTGTTGGG | 10580 |
rs545202032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345069 | ATTCAAAGAAATAAG[C/T]GTATTAATTAAATTG | 10580 |
rs545207288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541031 | GCCCTCCCCCAGGCT[C/T]CTGCTCACTCCAGGA | 10580 |
rs545218556 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442875 | TGGAATCATGTTGAA[C/T]CTATAGATCAATCTG | 10580 |
rs545226334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410013 | CAGTCAGAGACACTA[C/G]AGAAAACAAACATGA | 10580 |
rs545240761 | snp | A/C | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561501 | CGTCCACTCTGGCAG[A/C]GCCCGGCCAGCGGGC | 10580 |
rs545242935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548177 | TTGTGACACTCAGAG[A/G]ACTTCATGGACATAC | 10580 |
rs545245998 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529925 | GAACCTGCAAAAGAG[A/G]TCCCCTGGAAGGAAG | 10580 |
rs545249859 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367468 | AAGAGGAGGACAGAA[C/G]AGAAGAAAAATAATT | 10580 |
rs545258083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509248 | CCGCCCCCTTGCCCC[A/C]AGTTTTCCAGAGGCC | 10580 |
rs545274167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555522 | GTATTCAACAGTAAA[A/G]CAACTTAAATACTTT | 10580 |
rs545281147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408280 | AAGACTCTCAGGATC[C/T]GACGCACATAGACTG | 10580 |
rs545292297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448918 | CATAAGACCCTGCAG[A/G]ATCATGTCCCAGTTA | 10580 |
rs545302654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401532 | TATGGACAGGTTCTC[A/G]TCTTTAAGAAAGGAA | 10580 |
rs545305753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416263 | AAAGAAGGACGATCA[C/T]TAGAAACGACAGCAT | 10580 |
rs545309561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324412 | TCCCCTGGAAATGTC[C/T]TCAACCGTTAGCAAG | 10580 |
rs545318457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449481 | CAAGTGATCCACCCG[C/T]CTCGGCCTCCCAAAG | 10580 |
rs545321738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537781 | GGGCCACTGGAGAGG[A/T]CAGAAGGTGATCCAG | 10580 |
rs545333256 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549189 | GACCGTAGGGCAGTC[A/C]CTAGCCACACGTGCC | 10580 |
rs545351779 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314259 | CTGTCCTGAAGGTAA[C/T]CATTTCTAAAAGCCA | 10580 |
rs545354064 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442160 | ATAAATGGTATCATA[C/G]TACAGGTAATCCTTT | 10580 |
rs545360465 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516262 | AAATTCTGGGGGAGG[G/T]ACCCAGCAATCTGTG | 10580 |
rs545371724 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375406 | TAGAATTCCTTACTC[C/T]CATTTCAAACTTTGG | 10580 |
rs545378085 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399583 | CTGTTCTAGAAATTA[A/C]GGAACAGGTAGAACC | 10580 |
rs545380312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494891 | TTTATTTATTTGTTT[A/G]TTTATTTATTTTGAG | 10580 |
rs545390512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485790 | AAAATGTATTCCACT[C/G]TCTATTTGTAGTCAC | 10580 |
rs545409720 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373470 | AAGGTATCTTTTTAG[A/T]CAGGATCTTGCTGAA | 10580 |
rs545411696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543331 | TTGAACCTGGGAGGC[A/G]AAGGTTGCAGTGAGC | 10580 |
rs545418568 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343050 | GCTAATTTTGTGTGT[A/G]TGTTTTTTTTAGTAG | 10580 |
rs545431495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424041 | ATTCACGTATAGCAG[C/T]GGTGTAGCTGCATCA | 10580 |
rs545453906 | in-del | -/GTGTTAGGATTACAG | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329470 | TGCTGGCCTCTGAAA[-/GTGTTAGGATTACAG]GTGTGAGTCACCGTG | 10580 |
rs545482848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345586 | CAGATGCACAACCAT[C/T]CATCTGCAGGACAAT | 10580 |
rs545494029 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452060 | GTACAGACCCATACC[A/G]TGCTCAGGAATGAGG | 10580 |
rs545499292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471261 | CTCTAATTCACTCAT[A/G]TACAGGCATTTATTC | 10580 |
rs545523902 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384575 | AGCCAAGGGTCCTTC[G/T]CTAGAGAATCCACAC | 10580 |
rs545527242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444574 | CTAATTTTTAAATCA[A/T]GTATTTCATGAACAT | 10580 |
rs545541526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520795 | TGCTCCCACAATCTG[A/G]CCATAAATGCCTGGG | 10580 |
rs545549214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479442 | AGGGGAATATACAAG[C/T]GCTAAGGGAAACAAT | 10580 |
rs545554384 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472518 | CAGAAACAGGCAGAG[A/G]TAAGAATAGCTTAGG | 10580 |
rs545573668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529579 | AAAAAGGTTAACTGT[A/G]TGAACGCAAAAAAGG | 10580 |
rs545589786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458041 | AAAAAAGCATTTCAG[A/G]GCTGGAAAAAAACAC | 10580 |
rs545594489 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550224 | CAATCAACTCAGTGT[A/G]GCCCATGCCAAAACA | 10580 |
rs545628910 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489242 | CTGCACAAAACCAAT[C/T]TCCTTCTTTTTCTCT | 10580 |
rs545638150 | snp | C/T | 0.000132118 | 0.00812659 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394581 | GTAGCAGCACCAGTA[C/T]GGAGAGGCACACAAT | 10580 |
rs545669217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372651 | ACTAGACCTTGATAG[C/T]GGTAGAAACATACTT | 10580 |
rs545692984 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332990 | ATCAGAATATTTTAC[C/T]CCAAAATATATTTTT | 10580 |
rs545724361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556222 | TTTCTATAAAAAGCC[A/G]CTGCTGACCACAGAA | 10580 |
rs545726346 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369704 | TCTGCCCTCCTCACT[A/G]CATGCTGGCACACCC | 10580 |
rs545727205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426044 | TTTCCTCCAGCTGTT[C/T]TTTATTTGCAATCTT | 10580 |
rs545741368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431209 | TCCCTCCCTTTCCTT[A/C]AAGAAAGCAAGCTCC | 10580 |
rs545755822 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381136 | AGAGATGTAAACTTG[A/T]ATAGGGAATCATAAA | 10580 |
rs545760605 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499535 | GTAAATGGCCAAGGC[C/T]CTCCGATTCATCTCC | 10580 |
rs545760802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465090 | TTCCTACAGACCAAA[C/T]GGTAAGGAGAACGTC | 10580 |
rs545761732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473546 | GGCAGGAGAATCGCT[G/T]GAACCTGGGAGGTGG | 10580 |
rs545765689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557218 | TGCCTTTGAATGGTT[A/G]GTGCTCTGGTCAACC | 10580 |
rs545780677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360871 | CAGGCTGGAGTGCAG[C/T]GGTGCCATCTTGGCT | 10580 |
rs545798332 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541574 | TCTGGCCCTAACATG[C/T]CTTTTTCATGCCACT | 10580 |
rs545811483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466227 | TGGGCTAATCACGAC[A/G]TCAGGAGTTCGAGAC | 10580 |
rs545827029 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426188 | ATCTTAGGATAATTT[G/T]CACTGAGTGAGTCTT | 10580 |
rs545831819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387963 | GGATAACATTGAGTC[A/G]CTCTTGCTACATCTT | 10580 |
rs545856812 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530262 | TCCCACCAGACACAA[C/G]CAGGTGTTCCTTCCT | 10580 |
rs545873002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459448 | GACAGAAAATCCCAG[C/T]GACTCCAAAAGTTAC | 10580 |
rs545877504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537032 | CACAGTGGGCCTGCA[A/G]GTGCCCAGCATGCCT | 10580 |
rs545918214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360375 | GTAAACTAAATTGGG[C/T]TTGAGGCTGCATCCA | 10580 |
rs545922901 | snp | A/C | 1.64806e-05 | 0.00287054 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351258 | ATATTGAGGAGGTCC[A/C]CAAAGCGCTCATTAG | 10580 |
rs545952936 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446324 | CCGCCAATTCCATGA[A/C]CCTATAATTCTAAGA | 10580 |
rs545956403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495902 | AATCAGAAGTTATCT[A/G]TTTCATGTTTGGGCA | 10580 |
rs545958212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551375 | CCTACCCCACACCCA[A/G]GTAAAATCCTCTCCA | 10580 |
rs545963215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425384 | CCTAGTTTCAGCCCT[A/G]AGTCTCTATCTTGCT | 10580 |
rs545981493 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374610 | GAGAAAAGAGAAAGG[A/G]TTAGGATACTGTTAA | 10580 |
rs545987152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523882 | TGTTAGCAGGGATAA[C/T]ACTGGAGCAGCAAGA | 10580 |
rs546000671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327070 | CTGAGCCCTCCCCAG[A/G]TACTCAGCATCTGCC | 10580 |
rs546007061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367323 | GCTGAGATTACAGGC[A/C]TAAGCCACCATGCCA | 10580 |
rs546029615 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405275 | AGACTCCAGCTCTAC[-/A]AAAAAAACTTTAAAA | 10580 |
rs546039784 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504007 | CAGGCCAGTTTCTGG[A/G]ACCCCTAATCTTAAT | 10580 |
rs546047899 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327146 | TCTAGTGTTAAGAAT[A/G]AAAAAGAATAAAGTT | 10580 |
rs546053171 | snp | C/T | | | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311311 | AGTGCCTTAACACAT[C/T]TGGTTTGGAGGAGAA | 10580 |
rs546056335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349605 | GGCTATGACTATAGG[C/T]GTGTGCCACCAAGCC | 10580 |
rs546068318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418102 | TTTTTTCCCGAGATG[C/T]AGTCTCACCCTGTTG | 10580 |
rs546103975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431667 | TGCAATTATCAACCC[C/T]ATTCTACAGTTCATC | 10580 |
rs546119156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489706 | ACTACAGAGCCCTTC[C/T]TGCCTACCAGATGGG | 10580 |
rs546123431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524368 | CACTTGTAGATAAGA[C/G]AGTGAAACAGAGTGA | 10580 |
rs546124452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473067 | AACGAAGAAACTAGG[C/G]TTTAAACTCAGGCCC | 10580 |
rs546126875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355795 | TGGCCATGGTGTGTC[A/G]GGAAGACAGGCGTGT | 10580 |
rs546127578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517086 | TACTTAGCCTTTCTC[C/T]GAGCCTCAGTTTCTT | 10580 |
rs546153114 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429611 | TCCTGTACCATCTTA[A/G]ATTTATCACCAATCA | 10580 |
rs546157996 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | SORBS1 | GRCh38.p7 | 10:95381762 | CTGCACGATATTTTC[C/T]TGTGTCTACTTTCTT | 10580 |
rs546161424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511349 | CCCAAGTAACTCCAA[C/T]TACAGGCATGCACCA | 10580 |
rs546171272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405194 | CCTATAATCCCAGAA[A/C]TTTAGGAGGCTGAGG | 10580 |
rs546174063 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95311898 | AGAAAAATCTATGTC[G/T]GCATAGGACATGCTC | 10580 |
rs546183773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452859 | TTGTATATGTGCCTG[A/G]TGGCTGCAGGAAAGC | 10580 |
rs546220451 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312912 | GCCGTGCAAATTGCA[C/T]GTGCATATGCATTTT | 10580 |
rs546220815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517925 | ATGCCCCAGGCTGCT[A/C]AAAGGGCATGTGCTG | 10580 |
rs546234860 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517223 | GAGGCCATATTCTAT[G/T]TTTGCCCTGAAACCT | 10580 |
rs546238873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412423 | CACAGAGGCTCCTCC[C/T]CTTGACAGAGGAGGA | 10580 |
rs546239241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418358 | GCTGGGATTACAGGC[A/G]TCAGCCACAGCGCCC | 10580 |
rs546253538 | in-del | -/ACGG | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560685 | GCGGCACGGGCAGGC[-/ACGG]GCCGTGTCCCCGGCG | 10580 |
rs546266142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517687 | GTAGAATGAATCACA[C/T]CAGAGCAGCTGGGCA | 10580 |
rs546271520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544986 | GCCCCCTCACACCTG[C/T]CATTGCTGGCTCACT | 10580 |
rs546271612 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494422 | TGCAAACCTGCCAAG[A/C]CTGGCTGAGCACCTC | 10580 |
rs546296238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512280 | AAAATTAGCCAGGCA[C/T]GGTGGCGCATACATG | 10580 |
rs546354543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375703 | GTACTTGTTGTTAGT[C/G]GGGGGAGGTCTAAGA | 10580 |
rs546364792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551924 | CTCTGAAAGACAAAA[A/C]TATAATAAAATGAAA | 10580 |
rs546396666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416965 | TGAATTGGCCTCTAC[C/T]GGATTGGACTGTGCC | 10580 |
rs546415459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439960 | GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10580 |
rs546428012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558448 | AAATTCCTCAGTTTG[A/G]CGGGGAAGGGGGAGG | 10580 |
rs546447245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446136 | CACAGCTTGGGTGTG[C/T]CAGCGGGGAGTCAAA | 10580 |
rs546454829 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524678 | AGTTACAACAGAGAA[C/T]GTATGGCCCGCAAAG | 10580 |
rs546469333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396690 | TTTTTAGTAGAGATG[A/G]GGTTTCTCCACATTG | 10580 |
rs546503973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391304 | ATGAGATAACAATAG[C/T]GATATATTCAGCACA | 10580 |
rs546540610 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454503 | AAGGCTGGAATACAG[G/T]TCCTGGCTCCGGCTC | 10580 |
rs546550485 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536861 | CTAGTAATAGTCACA[C/T]TGGGACGAAGCACCC | 10580 |
rs546586748 | snp | G/T | 9.88452e-05 | 0.00702942 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336741 | ATCTTGGGTCCACCA[G/T]GGCCTCTTTCGCCTG | 10580 |
rs546592087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453241 | CAGTGAACCAAGATT[A/G]TGCTACTGCAGTCCA | 10580 |
rs546592349 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367864 | AAGGAAAAGGTCTTC[A/G]GTGCTGGTGGAGGGT | 10580 |
rs546599261 | snp | A/C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343655 | TAAAAAAAAAATGAC[A/C/T]TAGATCTTTTTCATT | 10580 |
rs546621644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361180 | CATGACTCTTGACCA[C/T]AACTGGCTGCCTGAC | 10580 |
rs546622081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446795 | TCCTTAACTCCACCA[C/T]GGCTCCTTAAAAGGG | 10580 |
rs546623096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328956 | TCATTTTACAAATGA[A/G]AAAACGAAGACCTGC | 10580 |
rs546627906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466448 | CCATCTCCAAAAAAA[A/G]AAAAAGAAAAAGAAA | 10580 |
rs546646942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525804 | TATCTGTAGGACAGA[C/T]TCCACAAAGTGGAAT | 10580 |
rs546658181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559387 | CTTCCGAAAAGTATA[C/T]AGAAACTCTCCAACT | 10580 |
rs546669050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428187 | AGGCCAAGGCGGGTG[G/T]ATCATGAGGTCAGGA | 10580 |
rs546682289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504572 | AGACTCCACCACTTT[C/T]TATACGTGTATCCCC | 10580 |
rs546685511 | in-del | -/A | 0.243061 | 0.249904 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316452 | CCAAGACTCTATCTC[-/A]AAAAAAAAAAAGAAG | 10580 |
rs546724769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551154 | GATCCACTGATCAGG[C/T]AACTTACACCAGAGA | 10580 |
rs546742483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462362 | TTTATTTTTGAAAGC[A/G]TTTTTTAAACTACAA | 10580 |
rs546750910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468149 | TGATCCACCCGCCTC[A/G]GCCTCATAAAGTGCT | 10580 |
rs546752984 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343054 | ATTTTGTGTGTGTGT[G/T]TTTTTTAGTAGAGAC | 10580 |
rs546762435 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346311 | TTTTTTTAACAACAA[-/T]TTTTATAATTGTTAT | 10580 |
rs546810932 | snp | C/G | 0.000123663 | 0.00786232 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356754 | CTCATGGTACTGCTC[C/G]ACTTGCTGTCATAAT | 10580 |
rs546824370 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549490 | CATCTCCCACACAGG[A/C]ATTGATTCTTCATGT | 10580 |
rs546841103 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418492 | CCAGGTTCAAGCTAT[C/T]CTCCTGCCTCAGCCT | 10580 |
rs546852810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446305 | CCATATTGTCCCCCC[C/T]ACCCCGCCAATTCCA | 10580 |
rs546869158 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532613 | GAAATGCTGTGGCTG[G/T]CTCATTCCCAGCTTG | 10580 |
rs546876519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482274 | TAATTTTTGTCCTGG[C/T]CACAATTTTGACTCA | 10580 |
rs546876618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355482 | AAGTGCAGCCACTAC[A/G]AGCCATGATTAATTG | 10580 |
rs546878358 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461593 | ATACAACCAAGTGAC[A/G/T]GCAACACCAAGTATT | 10580 |
rs546878590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490764 | TTACTTCTTGCATGG[A/C]TTATCTCTTTTAGTC | 10580 |
rs546880030 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397977 | AACGTGACGGTTAGG[G/T]GTAAGGGTTTGGGAG | 10580 |
rs546899668 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430601 | ACCACCTCCATTTGC[G/T]GCCAGAGGACGGGAC | 10580 |
rs546929649 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348398 | ACCAAAGCAGCACAG[A/C]ATTCACACTTTGGTA | 10580 |
rs546964511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356053 | AGGTCTGCTGCTGCT[C/T]ATGCTTCCGGATGGT | 10580 |
rs546974266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352309 | GGAATAGAATTTTAA[A/T]GTGTTTTCTGATACT | 10580 |
rs546994350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507306 | ATACAGGCACTTAGA[A/G]GTGAGGGATGGGTAG | 10580 |
rs547005410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525215 | ACAGAGAAGGGTGCC[A/G]TCCTGACCACAAGGT | 10580 |
rs547010384 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447253 | GCAGGCAGACTGCTT[G/T]AGTCTGGAGTTCAAG | 10580 |
rs547016396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482775 | AATAGTGGAATTCTA[C/G]AATGTCAGAGCTTGA | 10580 |
rs547018929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362711 | CAAACACGCATTGCT[C/T]CCCCAGTCTCCAGCC | 10580 |
rs547022763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553512 | GGGGGCAGAGGAGAG[A/G]ATCTAATCCATAGTA | 10580 |
rs547023456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384953 | CACAACAGACCCATC[A/G]TCAAACGGCTTCCTC | 10580 |
rs547024670 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397365 | ATTTCAAAATCAAAA[C/T]GGAAAGTAACAATAT | 10580 |
rs547034542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377413 | TAGTGACCTTTACCA[C/T]CCCTTTTTCTAAGAT | 10580 |
rs547041594 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542259 | GCCCTATTTCCCCAT[A/G]TCCTCCCTGAGATCT | 10580 |
rs547056379 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357370 | GAGAGAGAGAGAGAA[A/C]GAGAGAAAGAGAGAG | 10580 |
rs547087777 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428898 | CCTTGGCAAGAGCCA[G/T]CCACTACCTCACACT | 10580 |
rs547096921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427440 | TGGGGGCAGGGAGTC[A/G]GTACTAAGATTACTG | 10580 |
rs547112276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492946 | AATGCCTACCTACGA[C/T]TCCCTGGAGTCTGCT | 10580 |
rs547116658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484019 | TGAGGTTGAGACCAG[C/T]TCGAGACCAGCCTGG | 10580 |
rs547120156 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519342 | TCCAGCACACAGACC[A/T]GTGCTGCCACCAGCA | 10580 |
rs547127909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471117 | GTTGAAAATACCATG[C/T]TCTATTATCACTTCA | 10580 |
rs547129737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323369 | GGAAAAATCTGCAAA[G/T]GACACACTCCAGTGA | 10580 |
rs547136808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351530 | GAGCCACAACTATTA[C/T]ACTCCCATCATAACC | 10580 |
rs547169760 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323824 | AAACCCCATCTCTAC[-/A]AAAAAAATACAAAAA | 10580 |
rs547174359 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454515 | CAGGTCCTGGCTCCG[G/T]CTCCTCAACCCAGGC | 10580 |
rs547179009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552859 | AACAAAGGAGACAGA[A/T]TGGAGGCCTATAGGA | 10580 |
rs547186555 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | SORBS1 | GRCh38.p7 | 10:95399163 | GTGCTGAGTCCTGCT[C/T]TCCCACTCTTCTTTC | 10580 |
rs547191565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414420 | AGAGCTCAGTGCTTC[A/G]GTGAGAAAGGGAATG | 10580 |
rs547217008 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315530 | CCTGAGATTTAGATT[G/T]TCTAAACCATGCAGT | 10580 |
rs547258821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513430 | GCTGCCGAGCCCTTC[A/G]TGTTTACCAGGAAGA | 10580 |
rs547286055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421497 | GCTGCTGGACTTAGG[A/G]TCTGGCCACAGCTAC | 10580 |
rs547290698 | snp | C/T | 1.6696e-05 | 0.00288924 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371323 | AGAAAAACTAGGAAA[C/T]ACCTGTGGCACGTTT | 10580 |
rs547314124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370240 | CTCCTCAGCTCCATA[C/T]TCCTTTTGTATCTTT | 10580 |
rs547333232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399926 | TATTGGGCAGACATT[C/G]TGCTCTGCCTTGTGG | 10580 |
rs547350144 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421172 | ACCCTGTCTTAAAAA[A/G]AGAGAGAGGAAGAGA | 10580 |
rs547353008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499955 | GAGAACACAGGATCC[C/T]GCTCTCAGCCATCAA | 10580 |
rs547368605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508762 | ATTCACAGTCTTCAA[C/T]TTTCTTACAGTGGAA | 10580 |
rs547372780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408952 | TGTGTCTCAGGCTGC[A/C]CAATTCTGATTTTTA | 10580 |
rs547378428 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534171 | TGCAGTGGCGTGATC[A/T]CGGCTCACCGCAACC | 10580 |
rs547380172 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463313 | AAAGCAAGACACTGA[-/T]TTTTTTTTTAAGCCA | 10580 |
rs547387995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547746 | ATAAATAAAGTATTT[A/C]TTAAGCCAAAGTTCC | 10580 |
rs547396120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393665 | GCTGAAGTGACCTTG[A/C]TGAACTCTCTGCCAG | 10580 |
rs547413070 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470101 | AATGACAAAAGGTTT[A/C]AGGAACTACACTTCA | 10580 |
rs547421211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434822 | GAAGTCGCCCACACA[A/G]CAAGAACAATACAAA | 10580 |
rs547434220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401055 | AGGAAGGAATGTACT[A/G]GATGGTAATTCAAGA | 10580 |
rs547434720 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365664 | CAGAGTAGGAGACAC[A/G]GGTTGTGATGCTACA | 10580 |
rs547436077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409533 | AAGTGAAAGAAAATG[G/T]TTTATTCATCTGCTT | 10580 |
rs547482419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555167 | GGATTACAGCTACCG[C/T]GCCCAGCTGAAAGGC | 10580 |
rs547490274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449913 | AGATAGACGGGTTAA[C/T]ATCCTTAATCTAATG | 10580 |
rs547501307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509320 | TACTTTTATGACCAA[A/G]GCAAAGGATAAAATA | 10580 |
rs547510559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534799 | TAAGGCAAACACAGA[A/G]GAGAAAGTGAAAAGC | 10580 |
rs547525719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493963 | TCAAGGACATGAATT[A/C]AGCATCCTCCAGGAA | 10580 |
rs547527515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415002 | CAGAGTACATGAGAC[A/G]GTCGGAGCTGGCCAG | 10580 |
rs547545559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536217 | ATTCAGGGCTGAATT[A/G]AGCTCTTTATATTGT | 10580 |
rs547586283 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349518 | CCATCCATGGTGGAG[C/T]GATGTGTTCATAGCT | 10580 |
rs547594196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406061 | TATCGGGCGGTGACC[A/G]GAAGACGGTTTCAAC | 10580 |
rs547613145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330671 | GTCTACCACCACGCC[C/T]GGCTAATTTTTCTAT | 10580 |
rs547643562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345180 | AAATTTTGGTCACTA[C/T]GCAAAATGTTTTACA | 10580 |
rs547643671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470889 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGTGCC | 10580 |
rs547656575 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524136 | GACGACTACAGACCA[A/G]TAATGGTTCCCGGCA | 10580 |
rs547658520 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499292 | TGGCTAGGCTGGTCT[C/T]GAACTTCTGACCTCA | 10580 |
rs547680272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338367 | ATCACCTGGTTCCAG[C/T]GAATGCAAATAATAC | 10580 |
rs547685394 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561531 | CGGTGCCGGGGGCGG[C/G]GCCGGGCCCAGCCGT | 10580 |
rs547697792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401680 | GGGGGAAACAATGAC[C/T]CCAGCATGCTCAGGT | 10580 |
rs547720528 | in-del | -/AGA | 0.0894459 | 0.191631 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488767 | TGCCACATGCAACCT[-/AGA]AGGCTCTACCTTCAA | 10580 |
rs547726427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317608 | TTTAGAATGTCTACA[C/T]GTATGCCTGAGTTTC | 10580 |
rs547747904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560759 | CGTCCTTGCGCCCCT[C/T]CCGCCGCCCTCTCCA | 10580 |
rs547749793 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443272 | GACCACCCTGGCCAA[C/T]ATGGTGAAACCCTGT | 10580 |
rs547764468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457227 | CACAACTTGTATCAA[C/T]AGAACACACCATGTT | 10580 |
rs547773348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529116 | AATGCAAATGACCTC[C/T]TCAGAATGTAGGAGG | 10580 |
rs547779908 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411351 | TATCCTACTGTGACA[-/T]TTTTTTTCACTCTAA | 10580 |
rs547782052 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325436 | AGTAAGAAGAACCTG[A/G]TATTTTACAAGCATA | 10580 |
rs547801394 | snp | A/C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541660 | GCCCAACATGCCCAA[A/C/T]CCCCAGAAACCAGTC | 10580 |
rs547817824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358713 | ACAGACATGCGCGCG[C/T]GCGCGCGCGCACACA | 10580 |
rs547818597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326096 | AGCCCTTTGACATCT[A/G]ATCTCCATATACTAC | 10580 |
rs547819175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346096 | GGGGCAGGGTATAAG[A/T]CCCCAACCTCTGCCT | 10580 |
rs547821787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423402 | GGCATACAATACCAT[G/T]CTTCTTTTGATTTTT | 10580 |
rs547847702 | snp | A/G | 3.35959e-05 | 0.00409839 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372092 | GAAATGAGCATAAAG[A/G]CATAAAGACAAACAT | 10580 |
rs547851275 | in-del | -/TTTTTTTTTCTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325555 | CCCAGGCACTACTTC[-/TTTTTTTTTCTT]TTTTTTTTTTTTTTT | 10580 |
rs547851841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549202 | TCACTAGCCACACGT[A/G]CCTACAGAGCATTTG | 10580 |
rs547892816 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458162 | TAACTCTCATCCTGC[C/T]AAGCCCTTCCAACAG | 10580 |
rs547967621 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373851 | TAGGATGCCTCAGAC[C/G]ATAAGGAGCTGTTCA | 10580 |
rs547989258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557262 | CTTTAATTGCTCATT[G/T]AAACATTCTGAGGCT | 10580 |
rs547993024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542916 | AGCATGACCAGGCCC[A/G]ATCCCTGCTAAGCAA | 10580 |
rs547997169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452048 | CAGACATCTGCAGTA[A/C]AGACCCATACCATGC | 10580 |
rs548035956 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558376 | GAGTTCCCACCCCAG[C/G]TCCACATCTTGCTAG | 10580 |
rs548037256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320347 | CTTCTCCAAGCCACG[C/T]TGAACCCCCTTCCTG | 10580 |
rs548057091 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502851 | AGCTCCTCTGGAAAC[G/T]TCCTTTTACTTTTCA | 10580 |
rs548065924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411243 | TGTAAGAACAGGGAG[A/G]AGTTGAGCAACAGTT | 10580 |
rs548066611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459067 | GGAGGAAATCCAGCT[C/T]AAGAAGCATGTAATT | 10580 |
rs548067066 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352990 | GGGTAAAGCTCCCAA[A/T]CTAGTACTTGAATCT | 10580 |
rs548074439 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487227 | TCATTTTCTAGAGAT[G/T]ACATGTTCCAGAAGT | 10580 |
rs548107368 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444138 | GTCTTGCACTATCAC[C/T]CAGGCTTGAGTGCAC | 10580 |
rs548155146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353545 | TCGCACTGTCACCTG[A/G]GCTGGTGTGTAATGG | 10580 |
rs548160313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348820 | GTGGTCACCCAAGTC[C/T]TACCGAATGGGATTG | 10580 |
rs548161155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424953 | ACCACACTCCCTGTC[A/G]CATCCAGACGGCTCC | 10580 |
rs548176557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466052 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATCGCTTA | 10580 |
rs548192318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465421 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCAGG | 10580 |
rs548203661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418137 | GGCTAGAGTGCAGTG[A/G]TGTGACCTTGGCTCA | 10580 |
rs548209431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479630 | CTGACCCTGAGGTAC[C/T]TCAGACCAGGGTGAT | 10580 |
rs548230442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366770 | CTCACTGCACCTTCC[A/G]CCTCCCAGGTTCAAG | 10580 |
rs548236630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339740 | AAATCAGAACACAAA[C/T]GTAAAGCAGAAAACA | 10580 |
rs548269407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516711 | GTATACTGGCCACAA[A/C]AGGGGTGAAATTGAC | 10580 |
rs548283091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496536 | GCTCTTCCACCTACT[C/G]CACTGATTCAGTAGG | 10580 |
rs548294645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439374 | GAGCAGTCTCCTGGG[C/T]TTTTCCACACCCATA | 10580 |
rs548299381 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508162 | AAGCTGGTCTTGAAC[A/T]CCTGGGCTCAAGCAA | 10580 |
rs548301534 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480694 | AACAAAAGAGTTATG[C/T]ATCCACTCAGCAAGC | 10580 |
rs548304352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472323 | TCTAAAGGGGTTTGA[A/G]CCCATGAGTACAGTG | 10580 |
rs548330394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390418 | ACATCAAATGTGCCA[A/G]GTGAGCCAACATCAT | 10580 |
rs548359336 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476934 | GAATGGCAAGTCTAA[A/C]ATGAGGAAATGTGAG | 10580 |
rs548376778 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429723 | CTGGCCCAAGTTCCT[C/T]ATACTTGATATGGGC | 10580 |
rs548389136 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403053 | CTGAGAGCTGGTGAC[C/T]GAGGATTACAGCAAT | 10580 |
rs548403694 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542801 | TCATTCTCCTGAGAT[C/G]GGCTTTAAAGAGCCT | 10580 |
rs548418476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417430 | GCCTCAGCCTCCCAA[A/G]TAGCTGAGACTATAG | 10580 |
rs548420563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496126 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 10580 |
rs548424948 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407122 | CAATCAGTGTGAACC[A/G]GAAGTAAACAGCGAG | 10580 |
rs548433430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446228 | AACACAGACATTCCA[C/T]GAGAAGAACAAGATG | 10580 |
rs548435799 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537320 | GGAGGTGCATGCACA[C/T]TCACATAACCGTGAT | 10580 |
rs548444388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510281 | AATTTTCTTTAACTC[C/T]TTGGGCTCATCTAAA | 10580 |
rs548447400 | in-del | -/CAGAGGGCTGCTGTCTT | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480425 | GGCACTAAGCAGACG[-/CAGAGGGCTGCTGTCTT]CACACACATAAAAGA | 10580 |
rs548449127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544261 | ACCACCCCCGACTAC[A/C]ACCCTCTGAGGCAGT | 10580 |
rs548452799 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519933 | TAAGTCAGCACCCAA[C/T]CTCCTGCAAAATCAG | 10580 |
rs548466547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525106 | CCCAGCATTCTGGGC[A/G]AAAAACAAAGCCGAT | 10580 |
rs548470814 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477734 | GCATTTATGGTCAGA[A/G]GAAAGTCCAAAAGGC | 10580 |
rs548480774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522785 | AATTTATTGGAGAAG[A/G]AAAGCTGAGCTCCAA | 10580 |
rs548487131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319716 | GCTCTGCTAAAACCA[C/G]AGGGACAACTTCACT | 10580 |
rs548509200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359866 | TGTACCCACCTGGGG[C/T]TAAGGGCTTTATATA | 10580 |
rs548509637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550535 | TGCTGCCTATTATTA[A/T]GTCTATCTCAGAATA | 10580 |
rs548509673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474532 | TCCTGTAACACCCAA[G/T]TCAAACACTGAAATT | 10580 |
rs548511121 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511290 | ATTTGCTGCAGCCTC[A/T]ACACCCCAGGCTCAA | 10580 |
rs548519465 | snp | A/C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369966 | CCCCTGGCCCTGCTG[A/C/G]CTTCCTCATGCTCTG | 10580 |
rs548520815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503520 | GCTGGGAGAAGTTAA[A/C]AATTACCTGAATATG | 10580 |
rs548537242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389218 | GATAAAAGGGTAAAG[A/T]TAGTCATACATGACC | 10580 |
rs548551197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488627 | AATATTGAATGAGCA[C/T]CTCAAACCTAAGACG | 10580 |
rs548561598 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535006 | ATCCTCACATATCTA[A/G]CACAAGTCCTGGTAC | 10580 |
rs548562499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538114 | GAGACTTTGTCTCCA[A/G]AAAAAAAAAAAGGTG | 10580 |
rs548573889 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428303 | TATAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 10580 |
rs548577010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396752 | TGATCCACCCGCCTC[A/C]GCCTCCCAAAGTCCT | 10580 |
rs548577251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467375 | CTTCAAAGGCAGAGG[C/G]TGGCTCTCCACACAC | 10580 |
rs548586952 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353974 | GCTTCAGACTTGAAC[A/G]TGACCAGGACAGAGT | 10580 |
rs548595924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382789 | AAGTTTTTCATGCAA[C/G]GCTGTAAACTTCTTG | 10580 |
rs548607420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432018 | TCTCCCCTGGCTGCA[C/G]CTCCAGCCCAGCCTG | 10580 |
rs548608669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512313 | GTCCCAGCTACTTGG[G/T]AGGCTGAAGGCCCAA | 10580 |
rs548641710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445700 | AATCCCAAGTGGCTC[A/G]GCAGTGGTTGTGTCT | 10580 |
rs548649741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505485 | AACTGCAGAGCCTCA[A/G]CCTTGGGTCCACAGC | 10580 |
rs548650753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368631 | GAAAAGGAAGAGATT[A/G]TGAAAGAGAGAAAAG | 10580 |
rs548662110 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313971 | GAAGAGAAGCCTTGC[A/C]AGGGTGTACTCAGAT | 10580 |
rs548674112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396324 | TCAGCTGGGGCAGAT[G/T]ATTGTTCGTATTAAC | 10580 |
rs548681697 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506499 | ACCAATCTGGGTCGG[G/T]TCCTGGTGGGGTTCC | 10580 |
rs548692274 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460572 | CAATAATTAGTCGGG[C/T]GTGGTGGTGTGTGCC | 10580 |
rs548700024 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391629 | AAGTTTTCTTTTTTT[-/A]AAAAAGAACATTTTA | 10580 |
rs548705099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438962 | TGTGTAATGAGGGTG[A/G]CAAACCACGCCCCAC | 10580 |
rs548718972 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492095 | TTATCAAAAATAATA[-/C]TTTCAGAGAAGTATT | 10580 |
rs548753305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498456 | AGTGATGGTTGCAAA[C/G]CTTTGTGAATATACT | 10580 |
rs548775761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95554012 | AGGAATGAGCCACTG[C/T]GCCCAGGCAGCCTTT | 10580 |
rs548787634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460238 | TATAAATTTATTCAC[C/T]AAACAGAGGGTTAAA | 10580 |
rs548793200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427123 | CAAAGCTAACTTTGC[A/G]TTCAAGAATCAGGCA | 10580 |
rs548812795 | snp | C/G | | | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337208 | GATCCACTCAGAGGT[C/G]ACAGCGTGCATCTCG | 10580 |
rs548821982 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377269 | TATAACACCTGAGGG[A/G]GGGGGTTGCCATGTG | 10580 |
rs548822396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412491 | CCCAGGGCCAAACCC[A/G]AAGCTATCAGGCCAA | 10580 |
rs548833440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401315 | AGTTCGAAGCTACAG[C/T]AAGCCATGATCATGC | 10580 |
rs548835737 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321003 | AGTGAACGTCTTAGA[A/C]CCTCACTGGCATCTC | 10580 |
rs548853750 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525935 | GGGGGCTGGAATTTA[G/T]GTCCCGGATGGAAGA | 10580 |
rs548865405 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483592 | GCAATGGCGCCATCT[C/T]GGCTCACTGCAAACT | 10580 |
rs548866563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558482 | ATGGCAATCACAGAG[G/T]TCTTTTATAACTCTC | 10580 |
rs548874089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398405 | TGCCCATTGGAGCCT[A/G]TTCCCTGGAATTCCT | 10580 |
rs548898322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490892 | AGAATCAAGTAAGTA[A/C]CAAAACCCAGATATG | 10580 |
rs548902133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433760 | GAATGGACCTGCCTC[A/G]TCAGCACCTCTTGTA | 10580 |
rs548920623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539935 | GGAAAGAAACACACA[C/T]ACACACAGACCCTTT | 10580 |
rs548929629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558068 | CCAATGCAGGCGGAT[C/T]GCTTGAGTCCAGGAG | 10580 |
rs548931242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426673 | TCCACGCAGAGTAGG[A/C]AACAGAAGCTCCGCA | 10580 |
rs548932665 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406657 | TCTTTCCCATTGTAC[A/T]GAGGAGGAAACGAAA | 10580 |
rs548958434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421648 | TAAAAACGTCTCAGA[A/C]CTTTTTCCTACATAT | 10580 |
rs548962786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322929 | ATGACACCAGATACC[A/G]GCGGCCTATGGCCAC | 10580 |
rs548966220 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435433 | GCCTGCCTGGGACGT[A/G]GTGAAGGCTACCGCT | 10580 |
rs548974828 | snp | C/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312755 | TTTTATTTTCTAGCT[C/G]TATTTAAAGAGGTGT | 10580 |
rs549001595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323573 | GAGGCCAGCCTTCAC[C/T]TGGAGAGTGTTTGGA | 10580 |
rs549004951 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409907 | TCTGGAATTTTAAAG[C/G]AGAAGGGTCAACATA | 10580 |
rs549010988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454926 | AGCACCAAATAGCCC[A/G]TAGTTCTCATGATAT | 10580 |
rs549017284 | snp | C/T | 0.000361555 | 0.0134405 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356182 | TGTCAGTGGAGATAT[C/T]TGAACAGCGGTCCAC | 10580 |
rs549018554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490186 | CAAGACATGTACCTG[C/T]TGTGATGAGTAATTA | 10580 |
rs549034262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560585 | ATGCCCGGGGAATTC[C/G]GAGAAAGGAGTTGCT | 10580 |
rs549043163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440831 | TTTTATCAAATTGTA[C/T]ACTAAAAATATCTGT | 10580 |
rs549044943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361482 | CTACAACAATGCTGT[A/G]TCGCCCAGGCTGGAG | 10580 |
rs549075076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328978 | AAGACCTGCCGTGTG[C/T]GAATTGGGAATGTGA | 10580 |
rs549095624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559949 | CCTCCTCTCTTCGAT[A/C]ACCACCAAGATACCT | 10580 |
rs549099605 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439340 | CTTCCAACCCCCCAC[C/G]TGAGAGAGAGATTCT | 10580 |
rs549100759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545833 | TGTTATAAGCAATTA[A/C]AACCCCTGGCCATAA | 10580 |
rs549111896 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456907 | GGTAGCAAAAACTAC[-/T]GCTGAGAGAGAATCT | 10580 |
rs549123794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321691 | ATACTAGCACTGAAA[C/G]CAGTCAGCACAGCTC | 10580 |
rs549130932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462558 | CTTCTTGCTATAAAA[C/G]CTTTGAAATATGGTT | 10580 |
rs549177400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449095 | TCCCCAAATTTAAGG[C/T]CAATCCCAATAGCCA | 10580 |
rs549178769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343704 | TGGAAAGGTCTCCAA[C/T]TGTAACTTGGAAGGG | 10580 |
rs549183246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351649 | CAAACTACCTACCCC[C/T]GGCTCAGCCCAAAGC | 10580 |
rs549185295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360302 | TTGAAGGTATGGTGT[C/T]TGAAGCCCCTCCCAC | 10580 |
rs549216908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356587 | CAAAGTGGGAGGCAA[A/G]ATCCCGCACACTCGA | 10580 |
rs549231692 | snp | C/G | 0.00240577 | 0.0345991 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440208 | AAACACTGAGGTCAG[C/G]GTGTGGGCCTCAGCT | 10580 |
rs549250814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455644 | AGGATATACAGAACC[C/T]GTCTTCCACATTGCG | 10580 |
rs549254620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350249 | TACTGTACTGAAAGG[C/T]TATAAAACAGTACAT | 10580 |
rs549262643 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483786 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 10580 |
rs549266492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475311 | TGTGTATAGGCACAC[C/T]TGTATCTTTTATAGC | 10580 |
rs549271024 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447168 | AAACAAACAAAAAAA[A/C]ACAAAAAAACCCAGT | 10580 |
rs549286966 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404500 | TTTACACGTGTGGCT[-/T]TTTTTTTTTTTTTTT | 10580 |
rs549288475 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459968 | AAGTACTTCTGATCC[C/T]GCCTGGAAACAAAGT | 10580 |
rs549289547 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324020 | CCAGGGCCTTCTAGA[G/T]GGGCGCTTAGAAATC | 10580 |
rs549289881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315593 | AAAAGGAAATTCCTA[A/T]CCAGCTTGTGCCTAA | 10580 |
rs549300867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343209 | CCAGGACTCTTTAAA[A/C]AAAAAAATGAGACAA | 10580 |
rs549319502 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492137 | AATACAGTTGAAGCA[A/C]CCCACTTTCCACTAA | 10580 |
rs549328038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482952 | GAAATTCAGTCTCCA[C/T]CTGGGCTAGCATTTA | 10580 |
rs549340420 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350827 | AAGAATTGTGTAACT[C/G]TCCACACCATAGCTA | 10580 |
rs549346945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345788 | GTCATCAACAAAGTA[C/T]CTCTTCAAAGTGGGT | 10580 |
rs549354534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378393 | CCAATTAAGTAAGTC[A/G]CCTGAATGTGGTATG | 10580 |
rs549356185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329663 | CCTATATTTACTTGA[C/G]TATCTTAACATTTAA | 10580 |
rs549356408 | snp | G/T | 0.00119808 | 0.024446 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369727 | GCACACCCAGCAAGG[G/T]CTCTCACCACAGCCA | 10580 |
rs549365950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493019 | ACTAAGCCTTCAGGC[A/G]CAGTGGCTCACACCT | 10580 |
rs549394539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363363 | ACATTTGTAAAGTCC[C/T]GGAGGACCTCTACTG | 10580 |
rs549398184 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461746 | ACAGTTTTTCCTTTT[C/T]TTCCTGCAAAAATGT | 10580 |
rs549415543 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423729 | CTGTGAGTCACTGTT[-/A]ACGCCCATTTAGTTT | 10580 |
rs549418400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370396 | TACAGAGGCCTGCCA[C/T]CATGCCTGGCTAATT | 10580 |
rs549432140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477467 | GGAGCCCAGAAAGCC[A/G]GTCACAGCTTAAAAT | 10580 |
rs549436900 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431824 | AAGTGATGGGTTAAG[G/T]TGGGGAGATGGGCTT | 10580 |
rs549451014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547834 | ATCAGAGCTCTCTTT[A/C]TCCTCATGCAGCAAA | 10580 |
rs549456295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384742 | CTCGGGCTGCTATTG[C/G]GTGGGAAGGAGAGGC | 10580 |
rs549468242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344296 | TGAGAAATATGATTC[A/G]CTTTAGATCTTTTTT | 10580 |
rs549492777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377531 | CCAAGCTAGGTTGAA[A/C]TCGGAGGGAAAATCA | 10580 |
rs549509684 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345258 | CGCAGATAAAGAAAA[C/T]TGAGTGGGGGAGAAG | 10580 |
rs549534201 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386512 | GTGGTGGCATGTACC[C/T]GTAGTCCCAGCTACT | 10580 |
rs549537611 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497599 | CCACTTCGCCCTCCA[C/T]CACCACCAATGAGCT | 10580 |
rs549537891 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363533 | AGCTCTTTGGTTAGG[C/T]AAAGAAGGTTAATCA | 10580 |
rs549547415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379251 | CGGGCATGGTGGTGC[A/G]TGCCTGTAGCCCCAG | 10580 |
rs549554645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547499 | GCACTTTGGGAGGCC[A/G]AGGGGGTGTATCACC | 10580 |
rs549569112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470949 | CAGGAGAATTGCTTG[A/T]ACCCAGGAGGCAGAG | 10580 |
rs549580518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399275 | TAGCTGGGGGGAAGC[A/G]TGTCTGCTAATTCTC | 10580 |
rs549591375 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514807 | GTCACTTCGACTTCA[G/T]ATTCATACTGGGCCT | 10580 |
rs549606980 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326270 | TTATGTAAAAGATAC[A/G]GTGTACGGTAATAGC | 10580 |
rs549630296 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457509 | AGTGCTTGACACACA[-/G]GAAGAACTCAGTAAA | 10580 |
rs549638141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463080 | CTGTGCCTTGCAATG[C/T]ATTTCCCTTCCTTGT | 10580 |
rs549641103 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562338 | AAGGTCATTGCAAGT[G/T]GGGGGAAGGCACCGT | 10580 |
rs549643442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435746 | GCCTGTCAAGGCAAC[A/G]GAAGGGAGGCATGTC | 10580 |
rs549673712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508915 | GACAAAGGGCAGGAG[A/G]TGGGAGTTATTCACC | 10580 |
rs549680503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371083 | AGTTTCAATCAGCAG[C/T]CTCTCTGCATATATT | 10580 |
rs549692228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415960 | GGAACGTGGAGTCCG[G/T]AAGCAAGGAACCAGG | 10580 |
rs549698454 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561643 | CGCCGGTAACGGGCG[C/T]GCGGGCCTAGTAACC | 10580 |
rs549706078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471475 | GTAATCCCAGCACTT[C/T]GGGAGGCCCAGGTGG | 10580 |
rs549723083 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353591 | CTGCAACCTGCATCT[C/T]CCAGGTTCAAGCAAT | 10580 |
rs549729860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457259 | GAAGAAAAGAACTAT[A/G]TATTCTATTCCAATC | 10580 |
rs549741573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359216 | CCGTGCCTATTGATC[A/G]TTATCACTTCAATCC | 10580 |
rs549742664 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493753 | ACTAGTGGGCAGGTT[C/T]CTGAGTATGGCTGAA | 10580 |
rs549746441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436527 | GGTTCCTTTCACACT[G/T]TGCCTTGTCTTAAAA | 10580 |
rs549747059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401794 | TGATCCCTGGCATCA[C/T]CACCATCAATGTCAA | 10580 |
rs549759486 | snp | C/T | 4.9423e-05 | 0.00497082 | missense | SORBS1 | GRCh38.p7 | 10:95399052 | CATCCATGGAAACAT[C/T]GCTTAAGTCCTGAGT | 10580 |
rs549772143 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536067 | AGCCTCAAGAAGAGA[C/G]AGCCGTGCATGGCCT | 10580 |
rs549774638 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330699 | TATTTTTAGTAGAGA[C/G]AGGGTTTCGCCATGT | 10580 |
rs549781063 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386580 | GGCAGAGGTTGGGGT[G/T]AGCCAAGATTGTGCC | 10580 |
rs549808883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395163 | CACATACAATTTAGG[A/C]TCCTTGAATTCTGGA | 10580 |
rs549861714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534384 | TGGGATTACAAGCAC[A/G]AGCCACCGCGCCCGG | 10580 |
rs549878365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502686 | CATAATAAAAATTAA[C/G]TTAAAATGTTAGGGG | 10580 |
rs549879269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485373 | AAAGCCTAAAAACCA[A/C]TATCTTACTGATTAT | 10580 |
rs549888577 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463311 | TAAAAGCAAGACACT[A/G]ATTTTTTTTTTAAGC | 10580 |
rs549889051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410180 | ATTGTCTACACAATA[C/T]GTTTTCTTTTTTAAA | 10580 |
rs549904542 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551590 | TCAAGGATCAGCATG[C/T]ATGGAAGGATAGCTG | 10580 |
rs549918417 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367433 | AAAAGGTAATACAAA[A/T]CATCACAAAATTAAT | 10580 |
rs549956422 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311442 | ATGTTTTATAAAGCA[A/T]ATCTAGACCCATTAT | 10580 |
rs549969456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464794 | AGTTGGAACTATCTC[A/G]GGACCCTGTGAAGTG | 10580 |
rs549991500 | snp | A/G | 0.234109 | 0.249494 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358718 | CATGCGCGCGCGCGC[A/G]CGCGCACACACACAC | 10580 |
rs549991741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324670 | TGGCTCCAACACCAC[C/G]CACCCTCCACTCACT | 10580 |
rs549992453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416506 | TGCATCTTTATTAGA[C/T]ATCCTGACTCAAGAA | 10580 |
rs549992884 | in-del | -/TGG | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483110 | TTGGTTGGGCTTTCT[-/TGG]TGGTGGTGGTGGTGG | 10580 |
rs550022064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494654 | ACCCACAGCTGACTA[A/G]GGTCAGCCTTTCTGA | 10580 |
rs550028502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317644 | AGAGACATAGGCTCA[C/G]TCAACATTTTCTTGT | 10580 |
rs550030965 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509788 | AAAGAATCAGCTAAG[A/C]TTTTAAAGTGGCTGC | 10580 |
rs550042384 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447471 | TGAGACCCTGTATTT[-/A]AAAAAAAAAAAAAAA | 10580 |
rs550051532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530573 | AATACTTTAGTATTT[C/T]CTCTGCTCAAATCTG | 10580 |
rs550053997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331534 | GTGGACACCAGAAGC[C/T]TCACCCAAACAAGGA | 10580 |
rs550054759 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458703 | ACAAACAAATGTCCT[C/T]TGGTGCTTCTGAGCT | 10580 |
rs550063365 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555775 | GGTGCCCACCCTCCC[A/C]AGGTGGGCAGAAGAC | 10580 |
rs550076439 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562709 | ATCAGCAAAGATTCT[C/T]AGATGTCAGGGAACG | 10580 |
rs550087966 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480904 | GAAACAGTTGCCCGG[C/G]AGTGATTCCTGGGCT | 10580 |
rs550102276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438640 | AGGCCAGAAATCCAA[C/G]TACCTGCTCTAGTTC | 10580 |
rs550120182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430527 | TACACCTGGTGGGCA[C/T]TGTGTTCTACGTCAA | 10580 |
rs550124241 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454971 | AAAATCTTCATTAGG[G/T]GAAGTTAAAAGGGAA | 10580 |
rs550124249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555293 | GGTGCAGGGGGGCCT[C/G]GCCTTTGGGGACGTG | 10580 |
rs550161421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354346 | TTCTTGGTGTATCTG[C/T]CTTCTTCTGAATTGA | 10580 |
rs550210241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444248 | ACCAGTCATGCACCA[C/T]CACACCTGGCTAATT | 10580 |
rs550219404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425060 | CCTCACAGCTATCAC[G/T]TTTACCGTTCCATCT | 10580 |
rs550223772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543512 | TCACACCTTCCTATT[C/T]GTGAAATAGTTTTGA | 10580 |
rs550225287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550564 | TAAGCGACGGATTTA[C/T]TTTTGCAACACTGTA | 10580 |
rs550227783 | in-del | -/AAAACAAAACAA | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543412 | CTCAAAAAACAAAAC[-/AAAACAAAACAA]AAAACAAACAAACAA | 10580 |
rs550236896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488267 | ATGCAATCTTGAAAC[G/T]AATTTTCTTGATTTG | 10580 |
rs550311307 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312758 | TATTTTCTAGCTGTA[C/T]TTAAAGAGGTGTTCA | 10580 |
rs550311829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318487 | CGACAGGATTAAATA[A/C]GGAATTTTTAAACTC | 10580 |
rs550339525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487394 | TTCCACAAAAGGCCT[C/G]AGAAGACCACATGGG | 10580 |
rs550340488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549927 | GCATTTGAGTCCCCC[A/G]ACTCCATAAGTGGGC | 10580 |
rs550343405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431411 | GATGCAGCTAAAGTG[G/T]GAAAGTCACTGCCCT | 10580 |
rs550346523 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450513 | TGATTACAATTTTTT[A/T]TTTTTTTGAGATGGA | 10580 |
rs550361330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431914 | CCTGATCCTGCTCCC[A/G]CAGCTGGCTAGTGGC | 10580 |
rs550367430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557947 | TTCCTCCTCATGTTT[C/T]GCTATTCCATCTTAG | 10580 |
rs550368622 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446295 | ATTAATCATTCCATA[G/T]TGTCCCCCCTACCCC | 10580 |
rs550384474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381504 | TTAAAAGCAGACTCG[C/T]GGGACTTATTTTATG | 10580 |
rs550402135 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381874 | CGGTCTGACTTTGGA[C/T]GGCTGTAGTGTAATC | 10580 |
rs550418527 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492646 | GAAAAGATACTTCCT[A/T]GCATGGACAGAGGCC | 10580 |
rs550423724 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556501 | TCAGCCTCCTGAGTA[A/G]CTGGGATTACAGGCA | 10580 |
rs550438239 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553476 | TCTATAATGAGAGGA[C/T]AGGGAGAAAGGGAAG | 10580 |
rs550442110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452134 | AACACATAACTTAAA[A/T]ACTTCAGTTCATAAT | 10580 |
rs550469668 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404758 | TCTATTAAGCAGCAG[A/C]TCAGTGCTGAGCTGT | 10580 |
rs550473399 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312188 | TATTTTTGTGCTAAA[A/C]ATCTGTAGGTGAGTT | 10580 |
rs550477142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320797 | TAGCCCCCCGCCTTC[C/T]ACTCACCATTGACCC | 10580 |
rs550482749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437883 | AAGCCCCGCCCAGGT[C/T]CCCATCCCAAAATAG | 10580 |
rs550537414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347520 | GCTCACTGTAACCTC[C/T]GCCTCCCAGGTTCAA | 10580 |
rs550538331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342972 | GCAACCTCTACCTCC[C/T]AGGTTCAAGCAATTC | 10580 |
rs550551318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511613 | GCAGTTGCAGCCTTT[A/G]GGACTGAGTTGGAAA | 10580 |
rs550571013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459566 | GGAATGTGCCCTAGA[C/T]ACTGACCACATGGAA | 10580 |
rs550580723 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365968 | CCAAAATACCCAAAT[C/T]CCTGCTGACTTTCAA | 10580 |
rs550606533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411784 | AAATGTCACGTGACT[G/T]ACAGGTGGGATCTTT | 10580 |
rs550617776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367016 | TCTCAGTCACACTCC[C/T]CTCCCCATAAGAACC | 10580 |
rs550619084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333187 | TCTGACACCTTTAAA[A/G]GCCTAAAAGGAACAT | 10580 |
rs550628589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474573 | AATGTCCTGTTGTCC[A/T]CGTTTGAAGATAGGA | 10580 |
rs550630547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446636 | CCCCATCCCCAACAA[C/T]AGATTGTAAATATCT | 10580 |
rs550653410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532401 | GGTACCCACCCCACC[C/T]CCAGATGGCTCAGGA | 10580 |
rs550664060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511078 | TGTATCTTTTCTGTG[C/T]CACCTGTAACCTGAT | 10580 |
rs550675050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466398 | GTGAGCCAAGATCAC[A/G]CCACTGTACTCCAGC | 10580 |
rs550680072 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391684 | ACTCTATTTATAGTC[C/T]AAAAGTCTGGCCAAA | 10580 |
rs550695983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489930 | TCACAGGAGCACCTG[A/G]TCCACATCATAGGAG | 10580 |
rs550737421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462644 | ACTACATTTCCACAA[C/T]GACCACTCATATCCT | 10580 |
rs550767698 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467462 | TCTGTCTGCCCTTCA[A/C]GGTTCCCTGCTGCCT | 10580 |
rs550786066 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362375 | GCAAAACTAATAGGC[A/T]TGGGGAGATTGTACA | 10580 |
rs550799397 | in-del | -/T | 0.284471 | 0.247612 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332438 | CAGTCATTGTTTGTC[-/T]TTTTTTTTTTTTTTG | 10580 |
rs550803370 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459083 | AAGAAGCATGTAATT[A/G]TAGACTTTTTTCCTA | 10580 |
rs550823229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396796 | TGAGCCACCGCGCCC[A/G]GCCAGAGAACAGTGT | 10580 |
rs550830821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335896 | TGGGTCTTTGTAGCT[A/G]ACCCAGAGAGAAGAT | 10580 |
rs550831952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538211 | CCAGGTGATAGAAAG[C/G]AAGTGGCCGGCAAGG | 10580 |
rs550837946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360546 | CCACATCTATATAAA[C/T]GCCCAAATAGGCAAC | 10580 |
rs550853869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497344 | CTTGATTCTTCTCAA[A/G]TCTGTTGCTACTTAG | 10580 |
rs550858346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403937 | ATAACACCTCCTCCA[A/G]GCTGGGGCAAGGATT | 10580 |
rs550878628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367538 | ACATCATTCAGAGCC[A/G]TTAGGCTGATACAAA | 10580 |
rs550878805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355043 | AAAGAGTTCACCTTT[A/C]ATCTATTATAAATAT | 10580 |
rs550884777 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390932 | AATTACAGGCATGAG[-/C]CACCGTGCTGGGTCC | 10580 |
rs550910393 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453092 | GGTGTTTGAGACCAG[A/C]CTGGACAACATGGTG | 10580 |
rs550916373 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418564 | TGGCTAATTTTTGTA[-/T]TTTTTTTTAAGTAAA | 10580 |
rs550927879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335137 | GCCCACCCATGGGCC[C/T]ACATGTGCTTGGCTG | 10580 |
rs550933772 | snp | C/T | | | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95387029 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGTCTAGGA | 10580 |
rs550939726 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474501 | TTATTATTTTGAAAA[G/T]AGAGGGTGCCAAGTT | 10580 |
rs550943058 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527927 | TAATCCTGCATCTAA[C/T]TGATATCTCCATGAA | 10580 |
rs550947903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524853 | CACATAATAAACATC[G/T]GGTGAGTAAATGTAT | 10580 |
rs550948481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481396 | TCCATCTTCCTCAAA[A/G]CCACAATCACATCCC | 10580 |
rs550956599 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421045 | GGTGTCTCACACCTA[C/T]AATCCCAACACTTTG | 10580 |
rs550962098 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444827 | AATCACCGTCATATG[C/T]GGGTAGCCCTTTGCA | 10580 |
rs550973712 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367727 | AAAAAAGAAAAAAAA[A/G]AAGAAAAAAATAATG | 10580 |
rs551018444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559217 | CCCTGCCCTTTCATT[G/T]TTTACAAAGAAAACC | 10580 |
rs551082109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491291 | GTAGAACAAGGATCT[C/T]TAATTCACCAGCTGA | 10580 |
rs551084354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499218 | GCTGGGATTACAGGC[A/G]TCCACCACCACGCCC | 10580 |
rs551086919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397520 | AAAACAGTGGATGAG[G/T]ATACACTTGAAAGGT | 10580 |
rs551093600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349718 | CGTAAGTGATCCTAC[C/T]GGCTCAGCTTCTCAT | 10580 |
rs551108908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399632 | TACTTGAAAGTTTTC[A/G]ATTCCTCTTGAGGAA | 10580 |
rs551113879 | snp | C/T | 0.00138612 | 0.0262896 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377360 | AACACAGTTAACATC[C/T]CCTTTGCAGCTTGTA | 10580 |
rs551115071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526425 | TTTTGAAAGCGCCCC[C/G]CTCTCTCAGGCGCAT | 10580 |
rs551115227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384846 | TAACAAAGAAGTTCT[A/G]CAGCTAAGAGAAGAA | 10580 |
rs551126309 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319378 | CTTGCTAGTTGGCCT[-/A]AGGCATTGGGTCTGT | 10580 |
rs551141200 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363668 | GTTAATTATAAAAAA[C/T]ATATATATTGAAGGC | 10580 |
rs551142596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328776 | CTCTCTTAGGTGGAA[C/G]AGGGTAAGGTGGATA | 10580 |
rs551144395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558539 | TGTGTAACCATGAAT[A/T]AACCAGCAAGTTAAA | 10580 |
rs551168456 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519306 | AGCACCTGTGGATGT[C/T]ACCACCTCCTGCTGG | 10580 |
rs551169399 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540632 | TCCATGTCATTCTGG[A/C]AAGTTCTTTCTTCTC | 10580 |
rs551171181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455086 | GAGTTGCTGTTCTGA[C/T]GCTTACTAGATGTGT | 10580 |
rs551179627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420785 | AGGGAGAAAAACATC[A/G]TCTCTGATTCAGCTT | 10580 |
rs551242538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413259 | GCTCTTCTCCAGACC[C/T]ACTCAGTCAGAAATT | 10580 |
rs551252577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527275 | CTAAAAAAATACAAA[A/G]ATTAGCCAGGCATGG | 10580 |
rs551258362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520263 | AGGTTGCAGTGAGCC[C/T]GGATCACACCATTGC | 10580 |
rs551259337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552736 | ACAGACCCTCTCTCA[C/G]AAACTTGTGGAAGAA | 10580 |
rs551286294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429010 | GCTCCTAGGCCCCAG[A/G]ATAGGACAATAGACT | 10580 |
rs551302630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534076 | GAGGGGGTGGGACTT[C/G]GGGCCCCCAATCATG | 10580 |
rs551316540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420086 | GAGCAATTTACCAAG[C/T]TCCCTTAAAAGGGAA | 10580 |
rs551323504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407018 | CACAGCCGCTAAATA[C/T]AAAGCAGCCACATAG | 10580 |
rs551324258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552143 | CAGTGGCTCACACCC[A/G]TAATCCCAGCATTTT | 10580 |
rs551343995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507211 | CAAATACAGTTAGAA[A/G]ATACTTGTTCTGGTA | 10580 |
rs551346565 | snp | A/G | 1.73776e-05 | 0.00294762 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414865 | AGGAAGTGGCATCCT[A/G]TGGAAATAAGGGGGT | 10580 |
rs551366745 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318674 | TGATCACTCTTATTT[C/T]GCTTCATTTGGTTAC | 10580 |
rs551391518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316691 | CTTGAAATGTAGCTA[A/G]TCTGAAATGAGCTGT | 10580 |
rs551404379 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441011 | CTTTGGCATTCACCC[A/C]GGTGGCAAAAAATAA | 10580 |
rs551407970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415707 | GTGCGGGAGACAAGG[A/C]CGGGAGCCGGTGCTC | 10580 |
rs551422102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421758 | ACACCCTGGTACAGA[C/T]CAACCTCATTCCATG | 10580 |
rs551423113 | snp | C/T | 3.29707e-05 | 0.00406008 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95434641 | AGGGAGAACTAGGCC[C/T]GAGGCGTTTTTCACT | 10580 |
rs551457682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514978 | CACACTACAGCTTCA[A/T]CTCTCAAATATGGGG | 10580 |
rs551470894 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536303 | CTGACATCAAGCACA[G/T]TCATAACCTATTTTG | 10580 |
rs551495126 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540175 | GGTTTCAGACTCAGA[C/G]GAGCTCTAACGGCCT | 10580 |
rs551501028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456302 | TCTAGTTGCCATTGT[A/G]ATAATATTAAGAGGT | 10580 |
rs551507494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534732 | GTTGCAGTGACAAGG[A/G]AGGGGGCCAGAGCTG | 10580 |
rs551547550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329897 | TTGTTCTTATGCTTC[C/T]CAGACAGATGCTTTA | 10580 |
rs551548645 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447301 | GGGGATGCCCTGTCT[C/T]CACCAAAAATACAAA | 10580 |
rs551561335 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370494 | GTGATCCACTTGCCT[C/T]GGCCTCCCAAATTGC | 10580 |
rs551591652 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508008 | TTTTTTTTTTTTGAG[A/G]CAGAGTCACACCCTG | 10580 |
rs551604485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351435 | AGCATATTAGAAAAC[C/T]GCCAACAAAAGTAAT | 10580 |
rs551623732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476619 | TTATTTTCAAAGTAC[A/G]CTCATTTCCACTTCA | 10580 |
rs551652456 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462937 | TACCAATTTAGAAAG[A/G]AGGCAATGATCCAGT | 10580 |
rs551655079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343879 | CAGACAGGATTCTAA[A/C]TCTCAAGAGGTCCGT | 10580 |
rs551658694 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554174 | CTCCTGCCTCAGCCT[C/T]CAGATTAACTGGGAT | 10580 |
rs551671103 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441323 | GGCCAGGCTTCTGGT[C/T]TGTGGTCACCCACAT | 10580 |
rs551671420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317451 | GTTTGTTGAGAGAAC[A/G]TCAATAAAAGCATAT | 10580 |
rs551695965 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315446 | GGTCTTCTGACTCCC[A/C]GTCCATTGCTCTTTC | 10580 |
rs551733324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331636 | CCCACCCTCCTGCTG[C/T]ACATCTGTGAGAAAA | 10580 |
rs551744603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485552 | AGTGAGTCATCTCTA[C/T]GTTGATAAGGAGACA | 10580 |
rs551746110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324038 | GCGCTTAGAAATCTT[C/T]TGTGCATGACCCACT | 10580 |
rs551755368 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463185 | TGCCAAGTGCTCATG[C/G]AGTGTCTCCTTGGTA | 10580 |
rs551766866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449185 | TATTTTCTGTAGTTA[C/G]ACTGGCTAGAAATAG | 10580 |
rs551800357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364150 | TCTTATTCATTTGGA[C/T]AAACTGGGGGAAAAC | 10580 |
rs551817522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555146 | CCTCGGCCTCCCAAA[G/T]TGCTGGGATTACAGC | 10580 |
rs551818531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464149 | CATGGCAAAACCCCA[C/T]CTCTACTAAAAATAC | 10580 |
rs551825531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471554 | GAGACCCCATCTCTA[C/T]GAAAAATAAAAATAA | 10580 |
rs551827387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436622 | CTTTGAGATGCATCT[C/T]GACTTAAATGCCCAA | 10580 |
rs551830060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379022 | GCCAAGAGGGGCAGA[C/T]TGCTTGAGCCAAGGA | 10580 |
rs551836764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380181 | TGATCCCAAGAACTG[C/T]GGTATGGAAGATCCT | 10580 |
rs551840730 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522301 | TTCTTGAGTCCCTAC[G/T]TAACATATGCATGTT | 10580 |
rs551850336 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442272 | CTGTTTCAGTGAGCT[A/C/G]TCTTTATCTGATAAC | 10580 |
rs551852589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330507 | CTTTCCTTTTTTTTT[C/G]TTTACTTTTTAAAAT | 10580 |
rs551881016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477688 | GGCCACAGGAAGAAG[A/G]AATGGAGTCAAAGCT | 10580 |
rs551887509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417250 | GCGGCTCAACTGGGA[A/G]TTAGACTATGAGATG | 10580 |
rs551903653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528418 | TGTGCCTGGCCCAGC[C/G]CTTGTCCAAAATCCA | 10580 |
rs551908452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465384 | ATACAAAAAATTAGC[C/T]GGATGTGGTGGCGAG | 10580 |
rs551953555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365969 | CAAAATACCCAAATC[C/T]CTGCTGACTTTCAAA | 10580 |
rs551965053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352929 | CTCAAGGCCCCTTGT[A/G]TTCTGGCTGGAGTTA | 10580 |
rs551965508 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365608 | AGAGCTGAAGGCCCG[G/T]CTCAATTGGAAGCTC | 10580 |
rs551990899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500861 | CCTCCCCTGTACACA[A/G]GCATAACATCCACAC | 10580 |
rs552013426 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95561273 | CACCCCCGGCGCTGC[C/T]GCCGCCGAGCGGGCA | 10580 |
rs552021848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430019 | TCCCTTAATTCTTCC[A/G]AGTACAGTATTTGCA | 10580 |
rs552024087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346545 | GCAAAGCAGAAAAAT[C/T]CACTCTAGCCAGTTT | 10580 |
rs552032953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457127 | TGGAATAAAAGGTGA[C/T]AGAGTTAGGGATGTT | 10580 |
rs552036651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321517 | TCTAATTTGTCTTTC[A/G]GTGTTTGGTCCAAAT | 10580 |
rs552048008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500259 | ACAAAAAGATCACCT[A/G]GGGCTCCAGCCTGAT | 10580 |
rs552058631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509745 | AGTAAAACATACAGG[C/T]TACTATCAAATGTGG | 10580 |
rs552079308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325974 | AGGAAGAGACAAAAC[A/G]AAAGAGGCCATTTCA | 10580 |
rs552093652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472204 | AAATATTTAAGTATT[A/G]TAAGATTCTAAATTA | 10580 |
rs552094882 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492300 | GTAATAAGTAAGCAA[C/T]GTTCAACAATAAGAT | 10580 |
rs552106694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529061 | AAAGCGGAGATTCCA[C/T]TTGTCAGAGAAGTTG | 10580 |
rs552118120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319557 | ACTCTGTTTACTATT[C/T]TGAGACAAGACAGTA | 10580 |
rs552121698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493885 | CCTCCTCACAGGTGA[C/T]TGCGATGTCCAATAT | 10580 |
rs552125491 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321626 | GAATGAAGCAACCCT[C/T]TCATTCACGGCTGGT | 10580 |
rs552125661 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466562 | CCACAACACTGAAAA[A/C]CCACAAAAGGAAGGA | 10580 |
rs552142291 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421626 | TTACACTCTAAAGAA[-/T]TTTTTTTAAAAACGT | 10580 |
rs552143839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486230 | GTAGCTGGAATTCTT[A/C]AGATAAAGAAAATGG | 10580 |
rs552152319 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358707 | ACATGCACAGACATG[C/T]GCGCGCGCGCGCGCG | 10580 |
rs552156662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386961 | TACAAAAAAATTTTT[A/T]AAAAATTAGCCATGC | 10580 |
rs552164144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380695 | TCCTAATTAAAATGA[C/T]TTATCCTTCAGTGCT | 10580 |
rs552168268 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536075 | GAAGAGAGAGCCGTG[C/G]ATGGCCTAAAAAGGC | 10580 |
rs552172609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420898 | ACCTGCAGAATTTGC[A/G]GACTCCTTGTGAGTT | 10580 |
rs552179886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388211 | TCTCGAACTCCTGAC[C/T]GCAGGTGATCCACCC | 10580 |
rs552201084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345954 | AGATTTTAATCTCTT[A/G]GGATGTTGTAGCAAA | 10580 |
rs552210145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424883 | TCTCTCCAATTGAAG[A/C]ATTGGAGAATCTTTG | 10580 |
rs552228510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373774 | GAAGTGAAGAAAAAA[G/T]TTATCCTTACCACAC | 10580 |
rs552232958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547858 | CAGCAAAATGGGGCA[C/T]CCCTAAAACACTGTG | 10580 |
rs552253038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403808 | GTTGTGATCCACCTG[C/T]CTCAGCCTCCCTAAG | 10580 |
rs552271388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503358 | GACAGAACCCCAGCA[C/T]AGCCATTAATAAACC | 10580 |
rs552272132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496010 | GCTCAGAGCAACCTC[C/T]GCCTTCCAGGTTCAA | 10580 |
rs552275531 | snp | A/G | 0.000379435 | 0.0137686 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354850 | TACATTTTTCCAAGC[A/G]AAAACTAATGGATTT | 10580 |
rs552278071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487619 | CAAAAATGTCTATGG[A/C]AGCTGGAGACTGCAA | 10580 |
rs552286354 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370345 | CCTCCCGAATTCAAG[C/T]GATTCTCCTGCCTCA | 10580 |
rs552291931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445678 | GACATGAGGCTGACC[A/C]GATCTGAATCCCAAG | 10580 |
rs552293420 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449980 | ACGTGAAGAAATGAT[A/T]CCCAGAAGACAAAAT | 10580 |
rs552302418 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504537 | ATCTTAACCTGAGTG[C/T]CAACTAAAACTATAT | 10580 |
rs552314525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396201 | GCTGGGTCACCTGCT[A/G]ATAGCCCAGCCGGCA | 10580 |
rs552365981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382619 | CTTTGTGGAAAATAA[A/G]TTCACAATAGGTGTG | 10580 |
rs552367020 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458958 | AACAAAAATCCTTCA[C/G]GAAAAACGTAACTTT | 10580 |
rs552376819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409780 | CAAGCCCTTTCTACA[C/T]GAGGAAACAGCTTGA | 10580 |
rs552381083 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95546363 | TGGTTCATGGTTCTG[A/C]AGGCTGTACAGGAAG | 10580 |
rs552386769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417320 | TGTTTTATTTTGTTT[C/G]GAGATGGAATCTCGC | 10580 |
rs552409883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424391 | CGCAAAAACTGCGTG[C/T]GGTCAGCCCTCCATA | 10580 |
rs552425837 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540257 | GTGGCAGCCGCAGCC[A/G]CGTTTTAGGTAAGTG | 10580 |
rs552430504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523436 | CAGGGACATGCATGT[A/G]TTGCATTAAGAAAAA | 10580 |
rs552432580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516284 | CAATCTGTGTCTTAA[C/T]AAGCCTTCCAGGTCA | 10580 |
rs552432725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451882 | AAAAAGCTGAAAAGC[A/G]GTCTGTTAGAGCTTG | 10580 |
rs552441391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389181 | TCCTCTGGCTTTACC[C/T]CCCACACTTAGGAAG | 10580 |
rs552449933 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531222 | AAGCGACTTGCCGGA[C/G]GTCACACAGCTCAAA | 10580 |
rs552454795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510199 | AAAAAACTGCTGGAT[A/G]ATATGAAAGTATTTC | 10580 |
rs552478251 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446152 | CAGCGGGGAGTCAAA[C/T]CGCCATTCCACGCTT | 10580 |
rs552498726 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450811 | CCGGCTCTGTGGTTA[C/T]AATTATATAATAGGC | 10580 |
rs552522921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416608 | TCAAGATTTATCTTC[A/G]AGCCTTTGGCCTTAG | 10580 |
rs552560858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544036 | AGATCTGAGGGGTAA[A/G]AGGCACGAACCAGGT | 10580 |
rs552564981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544183 | AATGCATAAACTCAG[C/G]AAGCCCAAGAAGGAT | 10580 |
rs552566120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473856 | TTTTAAATTTTGCAC[A/G]TGGTCAATTTTGTAT | 10580 |
rs552568302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348196 | AAAGGGCATAATTTC[A/G]CAGTTGCAGGTGAAC | 10580 |
rs552588775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524806 | ACTCCTTTATACCTT[C/T]GGCACTGGCATAGTG | 10580 |
rs552593530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492977 | GTCCCAGAGTCTGCA[A/G]GGCCTAAGAAACACA | 10580 |
rs552612167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410847 | AATGTTTTTTAAAAA[G/T]AAGAAATTTAAAGCT | 10580 |
rs552619689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451258 | TCCTAAAGAAGCAAT[C/T]GCACCAAAACATTTC | 10580 |
rs552625296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543703 | CGGTGAGGACAGCAG[A/G]GGTGTTTCATTCTCG | 10580 |
rs552627137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481107 | GGGCCCCTGTACCTC[C/T]CCTGCTGTTCACCTC | 10580 |
rs552636713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537812 | GAAAGACTCAGAATT[C/T]AATGACTGGATAAAA | 10580 |
rs552642515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402839 | CTGGTCTCAAAGTCC[C/T]GAGCTCAAGCAATCT | 10580 |
rs552654233 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378662 | CAAGCTGGGGAAATC[C/G]CCTTGTTTTACACTT | 10580 |
rs552658625 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502037 | CAGATCGATTCGACT[C/T]CAGGAGGCACAGACA | 10580 |
rs552669424 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311643 | TGTCTTCAAGGAGGC[A/G]GCAGAAGGCAGATGG | 10580 |
rs552680306 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404239 | GGGACAGCCAAGGAC[A/T]CCTTGAGGTCAACCA | 10580 |
rs552687455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354486 | AATGCTTTGTGCCAA[A/C]AGAGGGGTGGGCAGT | 10580 |
rs552703530 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447616 | CAGATCCACTAGCAG[A/C]GCCACGTTTCTCCAA | 10580 |
rs552706989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445775 | ATGAAACTACACAAA[G/T]TGAGCTTGACCGGAA | 10580 |
rs552720158 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486872 | TTCTACAGCCTCAGC[A/G]GTTTTTTTGTTTGTG | 10580 |
rs552721384 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311478 | TTTTATAATGTTTTA[A/C]TTTTGTTTTTAAAGA | 10580 |
rs552726330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425920 | ATAAATGTTACCTTA[C/G]AGCTCCCAAGCTGGG | 10580 |
rs552736927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334495 | AGGGGACAGGAAGTG[A/G]TACACTTGGGGTCTG | 10580 |
rs552741600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396454 | CAGAAAGGTACATGA[C/T]TGGTCCAAGGTTACC | 10580 |
rs552743349 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465391 | AAATTAGCCGGATGT[G/T]GTGGCGAGTGCCTGT | 10580 |
rs552744392 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533102 | CGCAGGGATCCACCA[C/T]CTTGTCTCACCACCA | 10580 |
rs552769004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538290 | CAAGGCAGTGCTAGC[A/G]CTCAATCAGTGTTAC | 10580 |
rs552771614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326795 | CTATCCTGTCCAAGA[C/T]TGTAGCCAGCAGCCA | 10580 |
rs552801303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334045 | GTCAGATTCTCAACC[C/T]ACCTCCCCAATACCT | 10580 |
rs552801509 | snp | A/C/G | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432343 | CACACACCCCCCCCC[A/C/G]CCAAGAGGTATCTGA | 10580 |
rs552830230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439074 | TGGAATTAAAAGAAT[A/C]CACCATTTTTACACT | 10580 |
rs552861484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431977 | TTTTCCAGGAGCAAG[A/G]TCATTGAGTCATCCA | 10580 |
rs552876765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466141 | CAACAGTGCAAGACT[C/T]GAAAAAAAAAAAAAT | 10580 |
rs552880606 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405548 | GATGGCCTAGGAATC[C/T]GAGTTTCGACAAGCT | 10580 |
rs552883608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445242 | AAATCTGCAGCAGGT[A/G]ATACTAACAAACAAG | 10580 |
rs552912811 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460510 | TGAGCTCAGGAGTTT[A/G]CGACCAGCCTGGGCA | 10580 |
rs552918474 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396062 | AGGATGCTCTGCCTG[G/T]GGGAGAAGTGGTACC | 10580 |
rs552921350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362222 | CTAACGGGCAGGTTC[C/T]GGAGGCAGTGGACAG | 10580 |
rs552922161 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517380 | CGGGTCCGGCCCTCA[C/T]CCACTCCTCACACCT | 10580 |
rs552942294 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398232 | TTTGAGGCTTAGTCC[A/G]CTGTGGTTTCTATTG | 10580 |
rs552949271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466918 | CCATCTCAAATTAAC[A/T]TTTTAAAGTAAAAAA | 10580 |
rs552953943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474153 | AGGAAAGAACTCCCT[A/G]TAAAGATTATAGGAA | 10580 |
rs552959349 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544299 | CCCTGCTACTGCCCA[C/G]CCTCTAAGCCAAGCA | 10580 |
rs552961835 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480807 | TATGCGAGAGACTTA[A/C]AAATGAGTCTGTACA | 10580 |
rs552975881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461102 | TTGCAATGCTGTTCT[A/G]AGTCAACTCTGATGA | 10580 |
rs552988803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524891 | CATCACTAATGACTT[A/G]ATGACAAGCTAGAGA | 10580 |
rs552999244 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490805 | ACATATCCTGTAAAC[A/C]GCAGGATATGTTTCT | 10580 |
rs553020401 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467162 | TCTTCATTTTCTAAG[C/G]ATTCCTATTAAAGTT | 10580 |
rs553020678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451663 | ACTCTGTTTAAATCA[A/T]AAATATATAACCTCA | 10580 |
rs553026067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355097 | TTAATGATCAATGGT[C/T]GAATTCTGAAGGAAA | 10580 |
rs553048079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367940 | CTACTCCTGGTCTTT[C/T]GCCTTCCAGTGGATG | 10580 |
rs553057711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327785 | CAAGTCTTCTCAGAC[C/T]CCACCCCACCTTTCT | 10580 |
rs553072766 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444372 | AAAGTGCAGGGATTA[C/T]AGGTGTGAGCTACTG | 10580 |
rs553084533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558734 | ACTAATCAAGGAAAA[C/G]GTAGATGTGAATCCA | 10580 |
rs553084711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371502 | ATGGAAGGTTACGTT[C/T]GAAAAAAATGAATTT | 10580 |
rs553086843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321207 | ATCTACCCTCCACTC[G/T]GTTGCCAGAGTTATC | 10580 |
rs553092004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524390 | ACAGAGTGAAGCTGC[C/T]TGCACCACTGTCTAT | 10580 |
rs553102443 | in-del | -/A | 0.472128 | 0.123118 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387125 | ACTTTGTCTCTAAAG[-/A]AAAAAAAAAACAAAA | 10580 |
rs553118587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480885 | AGAGGGCAGACAGCA[A/G]TCAGAAACAGTTGCC | 10580 |
rs553118701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342402 | GGATGGTGCCTGTTG[C/T]ACAGGTAGGTAACAC | 10580 |
rs553120086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496217 | CGTGAGCCACCGTGC[C/T]CCACCATGGGCAGTG | 10580 |
rs553126936 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556732 | ATTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC | 10580 |
rs553130540 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339955 | CTCCTTCTTTATCAA[G/T]AAATAGAATTCTAGA | 10580 |
rs553156244 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426801 | AGCTTTCAGTAAGTT[C/G]TGTGAGTCCCTCCAG | 10580 |
rs553162663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552173 | TGGGAGCCCGTGGCG[A/G]GTGGATCACCTGAGG | 10580 |
rs553181225 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454516 | AGGTCCTGGCTCCGG[A/C]TCCTCAACCCAGGCT | 10580 |
rs553183225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376196 | AGCAATCATCTGTTT[C/T]TACTGACAACAGCAA | 10580 |
rs553189465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489419 | GCTCACAATACTTAG[G/T]GAACACCCATCAGGT | 10580 |
rs553203175 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482574 | AGGATAATACCATGA[C/G/T]CTGGTGAGTACATAA | 10580 |
rs553216431 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492174 | TGCCATACATCAAAA[C/G]TGCTCAGTGTCCTAA | 10580 |
rs553231688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362507 | GCATCTTAAACTCAA[C/T]GTGTCCCAAACCATC | 10580 |
rs553245925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355807 | GTCGGGAAGACAGGC[A/G]TGTGGGAACCACGGG | 10580 |
rs553255788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473552 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTCG | 10580 |
rs553257082 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488664 | CAGAACCCTTAGGGT[C/T]CCTCTTTGCTCCTTA | 10580 |
rs553260958 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338505 | TGGGATTTATGACAC[A/G]GTGGTGGTACCCACA | 10580 |
rs553266246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490523 | ATCACAAAAGTCAAG[A/G]CAGGAAGCCCCTAAC | 10580 |
rs553270849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497636 | TCAACTCTCTGGATC[A/C]ATCATGCCTAAACCT | 10580 |
rs553278999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397850 | GAAGGTGACAGATAG[G/T]TGGCTAGATATTTTC | 10580 |
rs553314274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389636 | ACAGAGAAAAAAATA[C/G]AACTCTGAAGAAGAG | 10580 |
rs553321128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420383 | ATAGTGGAAGAGGAC[A/C]TGCTTCTACATTTGC | 10580 |
rs553323750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384555 | AGAAATGCATGGGGA[C/T]AAACAGCCAAGGGTC | 10580 |
rs553327000 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539283 | ACTCTGTTACGAGGA[A/G]CTATCTTGTCCACTC | 10580 |
rs553329015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558326 | ACAAAAAAACCCAGA[A/T]ACATCTGGAAACAAG | 10580 |
rs553338354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391822 | TAGAAATGTCTTTTT[C/T]ATACTGTATAAACAA | 10580 |
rs553351389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368924 | CCTTGAAAAAACTTT[A/G]ACCCTGTAGAGTCCT | 10580 |
rs553357778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453453 | AGCAATTCAGCTACC[C/T]CAGCCTCCCTAGTAG | 10580 |
rs553385085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377880 | TAAAATGTACCAGCT[C/T]TTTCGGGGAACTGCC | 10580 |
rs553401562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412197 | TCAGGCATACAGCTC[C/T]TTAAAGTATAAATGC | 10580 |
rs553406595 | snp | C/T | 0.000149163 | 0.00863478 | missense | SORBS1 | GRCh38.p7 | 10:95381699 | CCATCTTTTCGTTGG[C/T]CAGAACGGAAGACTT | 10580 |
rs553449230 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525983 | TGGAGCAAAGAGGGC[G/T]GCAGGGAAAGATGAG | 10580 |
rs553494144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428453 | AGAAGAAAGAGCTCA[C/T]TTAATCTCAACAACT | 10580 |
rs553531666 | snp | A/G | | | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415591 | AAGCCTGAGTCCCCA[A/G]GGAAGGACTCTCGCC | 10580 |
rs553531771 | in-del | -/TCGTATCATTAATTCCAGTTAGAAGTT | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410909 | AATCAATGAGATACA[-/TCGTATCATTAATTCCAGTTAGAAGTT]TAAGCCGGAATGCTT | 10580 |
rs553568914 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322313 | AAAAATAGATATTCC[A/T]GTAGTGGAGTGCAGG | 10580 |
rs553576109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519644 | TACCATAATCCTAGA[G/T]GCACTAAATCCAGCA | 10580 |
rs553577141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513858 | TTTTAAGTGAGCTAA[C/T]GAAATGCAGCAAGCC | 10580 |
rs553580563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398552 | TGTTCCCTACTCACT[G/T]TGGATGACATGTGAT | 10580 |
rs553586870 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561388 | CGCTGCAGCTGGCCC[C/G]GCTCTGTTTTTCTGG | 10580 |
rs553590417 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545838 | TAAGCAATTACAACC[A/C]CTGGCCATAATTCCA | 10580 |
rs553612546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475630 | CATCTAACAACCCTC[C/T]GTAAAGGTACTATTA | 10580 |
rs553614570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328371 | ACAAACAACTAGTTC[A/G]ATTGCTTACCATCTA | 10580 |
rs553615330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532940 | CCAGTGTATCGGTTC[C/T]TCTTTGTCTAAGAGA | 10580 |
rs553625795 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438484 | CCCCACCTGGTGCCT[A/G]GGCTTCCGCATGCTG | 10580 |
rs553638838 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330622 | TTCAAGCAATTCTCA[C/T]GCCTCAGCCTCCCGA | 10580 |
rs553647013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378587 | AGCTAAAGCAGGGCT[A/G]AATGACCATGCTGAA | 10580 |
rs553690727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540197 | TAACGGCCTCCCATC[A/G]CTGGCCTCTAAGGTC | 10580 |
rs553725673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406057 | TGAATATCGGGCGGT[A/G]ACCGGAAGACGGTTT | 10580 |
rs553734956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400334 | GTGATGTGGCCTAAT[A/G]TCCACCTGACTCTAG | 10580 |
rs553754922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547607 | GTGTGGTGGCGGGCA[A/C]CTATAAGCCCAACTA | 10580 |
rs553769056 | in-del | -/AG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474168 | GTAAAGATTATAGGA[-/AG]AGAGAGTTCAATGTT | 10580 |
rs553784748 | snp | A/G | 1.65146e-05 | 0.0028735 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336915 | ATGCCTGAAGATGGC[A/G]TGTGGACACCACCGT | 10580 |
rs553790401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350958 | CAGCCAATGGTCTAA[A/G]GCATGCAACAGGGGC | 10580 |
rs553792198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508267 | ATGTAAATATTTGAC[A/C]CTTTTGTGGAATAAA | 10580 |
rs553795683 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545950 | GAATTATCTTTTTAC[A/G]CATCAGACATACTGC | 10580 |
rs553805973 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447990 | TCCGTTCTAACCAAT[G/T]ATCTGAAATGGCCTT | 10580 |
rs553806916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441059 | TGGGGCCTTCAGGGT[A/G]CGTGGGAAATCTGGG | 10580 |
rs553825741 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533497 | ACACTATGCCACAGT[C/T]CAAAATGGACTTACC | 10580 |
rs553829254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526446 | TCAGGCGCATCCAAT[C/G]TGCAGGCAAGGCTGA | 10580 |
rs553834404 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441778 | GACTTTCTGGCCCAA[C/G]TTCCTATGCACTGTG | 10580 |
rs553835363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523570 | TTTTTAAAAAATACA[C/T]TTAGCACATGGTTGT | 10580 |
rs553836867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535128 | AGATGCCCAGGAATT[C/T]TGGCCAGCAAATCAG | 10580 |
rs553855185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492604 | GTTATGGGAGCACTG[A/C]GCAGGGGCACCTGAT | 10580 |
rs553858293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559663 | GGTGCCAACAGACCA[A/G]CCCTTCCCTTCTTTC | 10580 |
rs553871626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408125 | CTGCTTCATGTGTCC[C/G]TAAGTCTGGGAACCT | 10580 |
rs553876520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343937 | GAGAAGGAATGTCTC[A/G]GGCCACATTTTTGCC | 10580 |
rs553890177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370523 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 10580 |
rs553895685 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541504 | CTACCACCTCATGCC[C/G]AGGAGCTGAGGCTGA | 10580 |
rs553929626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331024 | CCCTGACTTAAATTT[C/T]TGTATGTGTTCTTCT | 10580 |
rs553932666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469316 | ATAGATTCTGGCACC[A/G]TGTCTGACTAAATCT | 10580 |
rs553961112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520447 | ACCAGCCTGGCTAAC[A/G]TGGTGAAACCCCATC | 10580 |
rs553964340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448462 | GGCTCCTATACACTC[A/C]GAGGGGTTGGCTGGG | 10580 |
rs553965480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315902 | ATCTCAAGCAGCCAC[G/T]ACCAATGGGTTGGAA | 10580 |
rs553972857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462734 | CATGCAAACTTTTTT[C/T]CTTTGGTCAGGGAGG | 10580 |
rs553981519 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472497 | CTGAAAGCTACTGAG[A/G]TGGTTCAGAAACAGG | 10580 |
rs553998862 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431541 | CCTGGAGAGGCCAAA[A/G]TAATCTAATCATAAT | 10580 |
rs554017586 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358897 | GGAATTCCTTCATCC[-/CT]CTGTTTCATTGTGAA | 10580 |
rs554025423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521425 | CTTCCTTTCTCTCTT[A/G]GCATTTTTTTTTTAA | 10580 |
rs554056325 | snp | A/G | 8.30213e-05 | 0.00644234 | missense | SORBS1 | GRCh38.p7 | 10:95339185 | GAGAAAGGCAGGTCC[A/G]TGTAATCCACAGGGT | 10580 |
rs554061156 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352791 | CTCATTTTCTGAAAA[A/T]CCATGTCAATGATAA | 10580 |
rs554063998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421869 | TATTCCGTTATCCAA[C/T]TGGGGAAGCAGGAAG | 10580 |
rs554079076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422823 | CTCCCTTCAGCCTTC[C/G]CAGCCACTGCCTGAT | 10580 |
rs554082907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329290 | GATCATGGCTCACTG[C/T]AGCCTTGACCTCCCA | 10580 |
rs554085947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436691 | TTTACTGGGATGAGC[A/G]TTCATTCCAATTCTG | 10580 |
rs554088325 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452581 | TTTCTTCAAACCAAG[A/C]TAAAACCACTAAAAC | 10580 |
rs554095551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527938 | CTAATTGATATCTCC[A/G]TGAAAATTAAACTTG | 10580 |
rs554099525 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377822 | AGACTATTTATAAAC[G/T]GCCCTCTGGGAATGG | 10580 |
rs554107589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461953 | TTGAAATGCACCCTA[C/T]CTTTAAGACTATTTC | 10580 |
rs554114326 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331170 | GGAAAGAGAAGTGAC[A/T]CAACAAAAGATACTT | 10580 |
rs554135102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555384 | TGGTTCTCAGCACCA[A/G]CAGGTTTGATGCCTA | 10580 |
rs554137026 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563015 | CACGTCTAGGCTGCT[A/G]TGCACCGTACTATAC | 10580 |
rs554147591 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547989 | CCTTCGATGCAGCCC[A/C/G]CTGCTCCACAGGGGT | 10580 |
rs554195662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470642 | AAAATAGTTCTCATG[C/T]AAGTGCCTTTCTAAT | 10580 |
rs554239166 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95422760 | CATAAACATTTCAAA[A/C]TCTAATCACCCTTCC | 10580 |
rs554255684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324748 | TCCAAGTACCTTCTA[C/T]GTGGGCTTTCAGAAG | 10580 |
rs554259335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416835 | ACATGTGCTCTTTTC[C/T]CAGAGGAAAGAATTT | 10580 |
rs554274196 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425645 | TTTTTCTTCTCATTC[C/T]AAGTCTTTAAAACTG | 10580 |
rs554289376 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357683 | ACTCAGGCCCTGAAG[A/G]GGGATGTCACCACCT | 10580 |
rs554302992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528653 | GCTGGGCGCAGTGGC[C/T]CACGCCTCTAATCCC | 10580 |
rs554304357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318800 | TTTTGTGGGAGACAA[A/T]TTTTCCACAGATGGG | 10580 |
rs554320588 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484647 | CAATGTCCAGAAACA[C/T]GAAATCTGCTGGAAA | 10580 |
rs554333812 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512484 | CACAATTCTAAGTAC[C/T]ATAAGAAGCTTTCTG | 10580 |
rs554338606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351752 | GGCAGCAGGAGGCTG[G/T]AAGTGCCATCTCTAC | 10580 |
rs554350593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358266 | CAAGTCCACTACCTG[G/T]ATTATTTTTCTTGGT | 10580 |
rs554369367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501324 | AAAGACCAGCCTCAA[C/T]AAGGCAGGTGTGACC | 10580 |
rs554394184 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549051 | TTTCTGTGCCTCAGT[G/T]GCCTCCACCATGAAA | 10580 |
rs554395505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485633 | AATTAGTCAGTGGAA[A/C]AATCAGAATGATTTC | 10580 |
rs554397517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477031 | CCAAAAGAGAGCACA[C/T]TCCCAACACCGAGCT | 10580 |
rs554436011 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522188 | CAGAAGTTCTGACAG[C/G]GTCCCAAGGCCCAAC | 10580 |
rs554458698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386415 | CTGAGGTGGGTGTAT[C/T]GCTTGAGGTCAGGAG | 10580 |
rs554460146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486889 | TTTTTTTGTTTGTGT[A/G]TGTGTCTGTGTGTGT | 10580 |
rs554482151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445135 | GTATGACGATAGTAC[A/G]TGACAATGACAATGC | 10580 |
rs554497065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338777 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 10580 |
rs554507268 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365023 | TTCAGAGGATTAAAT[A/G]AGGTAAGGTAGATAA | 10580 |
rs554516643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395843 | ATATTTAGAGCACTT[C/T]GATATTTAGAAACAG | 10580 |
rs554578516 | in-del | -/TGGGGAGAGC | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467312 | GCCTTGCTCATGGCT[-/TGGGGAGAGC]TGGGGTTTTCAGCAG | 10580 |
rs554600080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409295 | AGAAACAAAATTTCA[C/G]TTTGTCCCACATTAC | 10580 |
rs554606858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543841 | ACTGGGGACATACTG[C/G]TGACAAGAAAGAGCC | 10580 |
rs554615815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549400 | AGCATGGACGCTGGT[C/G]TATAACCGGTGCTCA | 10580 |
rs554651002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333412 | TGCACCCCATTGGTT[A/G]GGTCTTCATTCTGAA | 10580 |
rs554655363 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440920 | TATAGCACAGTTCTT[C/T]GGCAATAGTAGTAGG | 10580 |
rs554655987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381046 | TAAGAATTCTTCCTG[C/T]TTCACAGAAGAGGCC | 10580 |
rs554679045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95416165 | CTTTTGAGGGAGAGG[A/G]GGGCGTGGGGGAGAG | 10580 |
rs554679445 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396207 | TCACCTGCTGATAGC[C/T]CAGCCGGCATCTGAT | 10580 |
rs554702469 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372344 | GAAAAGACGGGGGGG[A/G]AAAAAGAAAAAAAAA | 10580 |
rs554707071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511247 | TCTCATGCTGTTGCT[C/T]AGGCTGAAGTGCAGC | 10580 |
rs554730259 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495037 | ACTACAGGCGCCTGT[A/C/T]GCCATGCCCAGCCAA | 10580 |
rs554730556 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320113 | TAATTTGGGATGAAC[C/G]TCATACTCCTCAGAA | 10580 |
rs554746410 | in-del | -/A | 0.00159776 | 0.0282193 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558837 | ACAGGAAAGAACCTG[-/A]AAAATGCCATCACAA | 10580 |
rs554752710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543195 | ATTCCAGCTCACCCC[C/T]CAACCCACATGCCCT | 10580 |
rs554758694 | snp | A/C | 4.94262e-05 | 0.00497098 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437559 | CACCATCACATTCTG[A/C]AAGAAAGAAAGAGAG | 10580 |
rs554768668 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510716 | CATGGTGGCTCACAC[C/G]TATAGTCTCAGCTAC | 10580 |
rs554778752 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543323 | AGAATCACTTGAACC[C/T]GGGAGGCGAAGGTTG | 10580 |
rs554787306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502207 | TCCCCAATAATATTT[C/G]TGTCAGTAAAATGTG | 10580 |
rs554793466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387763 | TTACCATGTTATTAT[A/G]GAAGAGGCAGAGAAA | 10580 |
rs554810583 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340969 | CCTCAGCCTCCTGAA[C/T]AGCTGGGATTACAGG | 10580 |
rs554815826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523527 | CAACATTCCAACCAC[A/C]GTATTATTTTAGGAC | 10580 |
rs554836202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375212 | GACTTTAAAATAACT[A/G]GAGTTTTAAAGTCAG | 10580 |
rs554846107 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504152 | CAGAGTTCATTCTCC[C/G/T]TGGTCTGCAGATGAG | 10580 |
rs554854662 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524802 | TCTTACTCCTTTATA[A/C]CTTCGGCACTGGCAT | 10580 |
rs554859508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411446 | CCAGAAATACCAATA[A/C]AATTATTAATACTAA | 10580 |
rs554862391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401219 | GACCCCATCGCTACA[A/G]AAAATTAAAAAATTA | 10580 |
rs554890463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517574 | CCACAACCTCACAAA[G/T]CCCATGAAGTCAGGG | 10580 |
rs554895730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444387 | TAGGTGTGAGCTACT[A/G]CACCTGGCCTTTCCT | 10580 |
rs554924077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397122 | TGAGGTCCAACTGCA[A/G]GACCCAGTCTTCTGG | 10580 |
rs554993843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418476 | CTGCAACCTCCGCCT[C/T]CCAGGTTCAAGCTAT | 10580 |
rs555007877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425201 | GAAGGATGTAAACTT[C/T]GTACATGCAATTGGG | 10580 |
rs555019777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531794 | TGTTAGGATTTAAGA[C/T]AACATGCACAGGGGC | 10580 |
rs555056625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556995 | AAAAGAAATGGATAG[C/T]GGAGGGAGATGTAGC | 10580 |
rs555061484 | snp | A/C | | | missense | SORBS1 | GRCh38.p7 | 10:95339183 | AGGAGAAAGGCAGGT[A/C]CATGTAATCCACAGG | 10580 |
rs555065325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396546 | CACTCTTGTTGCCCA[A/G]GCTGGAGTGCAATGG | 10580 |
rs555065793 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549680 | AGTGTGGGAAAACCA[A/C]AAGAAGTTATGAAAA | 10580 |
rs555070210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545032 | ACATAGAGGCCCTGC[A/C]AAGCAAACACAAAAT | 10580 |
rs555071176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431012 | TGTGCCCTGGCACCT[A/G]TTATGGGTAGCTGGG | 10580 |
rs555074552 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363168 | CATCATTGCATTTAC[C/T]CCACTGGACTCTGGT | 10580 |
rs555098917 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379627 | AAGCAGACGTAAGTA[C/T]CTCAAATGGAAAAAG | 10580 |
rs555113269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390862 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCTTGAC | 10580 |
rs555120271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452124 | GTCTTTAGCAAACAC[A/G]TAACTTAAATACTTC | 10580 |
rs555130630 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324048 | ATCTTTTGTGCATGA[C/T]CCACTTGTTTCACAG | 10580 |
rs555135234 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338521 | GTGGTGGTACCCACA[C/T]CAACAGCTTCACCCA | 10580 |
rs555142569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431599 | ATTCCATGCCACCAG[A/G]CATGATACACAGCAC | 10580 |
rs555144009 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311694 | GGAGGGTATAAGAAA[C/T]TGAAGCAGTGAATTT | 10580 |
rs555188527 | snp | C/G | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489538 | TGTATCATTCCCACT[C/G]AAATCTAAGATCCAG | 10580 |
rs555194027 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557511 | GCAGAACTGAGTCCC[A/C]CCTCAGCATCAGCCA | 10580 |
rs555194065 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558786 | TGCTTCTTCTATGCC[A/C]TTGTGCAATACTTTG | 10580 |
rs555197238 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413751 | CAGTTGGGCTTTCCC[A/G]GCTGTGATGGGAACT | 10580 |
rs555205368 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509557 | TCCAAATAAGGAAAC[C/T]TTGTCCCTCTCGGAT | 10580 |
rs555207783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544642 | CAGGGAGGTCTGCAC[C/T]CTACTGTCAAGGGCA | 10580 |
rs555219201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446359 | TTTTGATGACACAAA[A/G]TGATTAATTACTAAA | 10580 |
rs555226422 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452376 | CATGGACCAAATCAG[A/G/T]TCATTAGCACCTCAC | 10580 |
rs555240038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366389 | TACAGGAAGGCTCCA[C/T]GAGGGCCTATCTATA | 10580 |
rs555263098 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471760 | CTTCTAGGGGACCGT[A/G]AGGCAGTGACAGGAG | 10580 |
rs555269210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551210 | AGGGAGGTAGAGAGA[C/T]GGGAGAGAGGGATGG | 10580 |
rs555270064 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372753 | TCTTTTAACTCTTCA[A/G]GTCAGATTTACAGCT | 10580 |
rs555276335 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95400977 | GGGGGTGGGTGCCAG[A/G]TTGCACAGAGGGTTG | 10580 |
rs555300008 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459255 | AATAAAAAACACTTG[A/T]ACTCTCAGAATGGTA | 10580 |
rs555312442 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320088 | GCTGCTTGGGTACCC[C/G]AGTCAGCTCTAATTT | 10580 |
rs555322013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488992 | GGACTATGGAATCCA[A/G]TCACTCTCAGAGTAA | 10580 |
rs555326986 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342524 | GCAGCCTCAACCGCC[G/T]GGGTGCAAGTGATCC | 10580 |
rs555360595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447072 | CTTGAACTCGGGAGG[C/T]GGAGGTTGCAGTGAG | 10580 |
rs555360784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341847 | ATTCAGGAAATTACA[C/T]CACATTTGGCATTTT | 10580 |
rs555375148 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551898 | AGTTGAAGATAAAGC[C/T]GAAGATAGCTCTCTG | 10580 |
rs555381244 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496307 | TCCCTTTTCTGACTT[G/T]GAAAAAGACTTCTCT | 10580 |
rs555406972 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404871 | CCAGAGACTTAGATA[A/G]CCTGCCTGAGGCAGC | 10580 |
rs555407337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321354 | GGTCCCATCCCACCT[C/G]TAAGCTTCATCTCTA | 10580 |
rs555442329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322236 | AAAGAGAGGAAGAGA[G/T]GTAACATTCCAGACG | 10580 |
rs555457643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481551 | GTGCAGACAAAACCA[C/T]GTATATCTCTGCTTA | 10580 |
rs555475232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412699 | ACTAAACATAAGACA[A/C]CTTACCTGCTACTCC | 10580 |
rs555480432 | snp | A/G | 0.000121337 | 0.00778806 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356423 | CTTGCTCAGCCTTCC[A/G]GACAGGTCCAGGGAT | 10580 |
rs555494038 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355118 | CTGAAGGAAAAAAAA[A/T]TTCCACCCCCCACCC | 10580 |
rs555499394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518340 | CCATATTAGGTATAA[A/G]TTTCTCTAAGAGTCT | 10580 |
rs555513459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383739 | CTTGGCTCCCATACT[A/T]GGAGCTAAGTGCTAC | 10580 |
rs555535828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420397 | CATGCTTCTACATTT[G/T]CTTTGAATTAATCAG | 10580 |
rs555541743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546862 | ATCCCTCAGCCTCCC[A/G]AACAGCTGGGACTAC | 10580 |
rs555543553 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458631 | GTCAGCTTTCTCCTA[-/A]AAAAAAAAAAAAAAA | 10580 |
rs555557773 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332451 | GTCTTTTTTTTTTTT[C/T]TGAGATGGGGTCTTG | 10580 |
rs555557863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344037 | AAGACCCTCAGCATA[C/T]TCACCCCTATGGAGA | 10580 |
rs555575574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376317 | ATGGACTATAGATGG[A/G]CAACTCTGCACCACA | 10580 |
rs555576466 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461163 | TTTTAAAATTATTCT[A/C]ACATGTGCCCTTCAA | 10580 |
rs555591976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474287 | TGAAATAGAAATGGG[C/T]ATGTCACCTCCATGC | 10580 |
rs555596219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475753 | AGCAGCCTGACTCGA[A/G]TTTGTGGTACTATAT | 10580 |
rs555599084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412804 | CAGCTGAAGGTAGAC[A/G]GGAATAGACCAGGGA | 10580 |
rs555627138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447579 | CCAGAATAAATGCCT[A/G]GCCTTATTTCTTTGT | 10580 |
rs555636797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376946 | TGGGATATAATATTT[A/G]ACCAAATAAGTATAA | 10580 |
rs555660007 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434022 | TGTGTAGGCCTCATG[A/T]GTCCCCACTTTGTAC | 10580 |
rs555660340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491429 | AAGTGTTACATTTCA[A/T]CTATGGATATGTTTA | 10580 |
rs555662968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466982 | TAACATATGGCATTA[A/T]GAAGAAACATAAGAC | 10580 |
rs555664587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392416 | TAGGCAGGAGTGGGG[A/G]CGTGAGATGGAATTT | 10580 |
rs555668828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433221 | GAAAACTCACAGCAA[C/T]AAAAACGACTCAGAA | 10580 |
rs555682480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540259 | GGCAGCCGCAGCCGC[A/G]TTTTAGGTAAGTGTT | 10580 |
rs555693831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461719 | CGCGTCAGAATTGCA[C/T]TAAGCAGGGAGACAG | 10580 |
rs555728389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474854 | GTTTACACTCCCTGA[A/T]ATATGGTTCTCCTAA | 10580 |
rs555729566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384657 | TGAGATGGATCCCCG[A/G]CTGCACCAGCTCAGT | 10580 |
rs555764493 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433980 | ACACAGCCCAGTTAC[A/T]TCTGAAAGCGCCATT | 10580 |
rs555801287 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352989 | GGGGTAAAGCTCCCA[A/G]TCTAGTACTTGAATC | 10580 |
rs555802746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483468 | ATACTTTTTAAAAAT[C/T]ACATTGTTGCTTTCT | 10580 |
rs555807340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470329 | TTTGGAGCTGGAAGA[A/G]ACCTGGCCTGTATGT | 10580 |
rs555839737 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497744 | CCCTCACCATCACCA[C/G]CACCCCACCCCCAGG | 10580 |
rs555847179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520488 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCGCAC | 10580 |
rs555870817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469421 | GCTAAGCCAACATTT[C/T]CCAAAATGTGTTCCA | 10580 |
rs555872442 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95422751 | AATGAGGCACATAAA[C/T]ATTTCAAAATCTAAT | 10580 |
rs555899730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364344 | CACGCACATTCACAG[C/T]GTCTGAAAACAATTT | 10580 |
rs555911898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508357 | GGTCACTGCAATGTT[A/C]TCGACTAATGGAGTA | 10580 |
rs555918753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462805 | GCAGCTAAATTTGAT[C/G]TATTTATTGCTAGGG | 10580 |
rs555925631 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496203 | GCTGGGATTACAAGC[A/G]TGAGCCACCGTGCCC | 10580 |
rs555941537 | snp | A/G | 1.78726e-05 | 0.00298931 | stop-gained, intron-variant | SORBS1 | GRCh38.p7 | 10:95337021 | GAGAAGCTACTGATC[A/G]TGGGGTGGGACGATC | 10580 |
rs555943434 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467718 | GAAGTATTCTAATTG[A/G]GCATTAAAAGCCGCC | 10580 |
rs555982455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514509 | TCAAGCCAATTCTAG[A/C]CCCTTATTGCCATGG | 10580 |
rs555983289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400630 | AAAAGTGATGGCTGA[C/T]GCCAGGGAGATGGCA | 10580 |
rs555986212 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527895 | CTTTTCCCCTCTCTG[C/T]CATTCTGCATTGCAA | 10580 |
rs556041934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492370 | ATTGATTCATTCACT[G/T]AACAAATATTTATTG | 10580 |
rs556045883 | snp | G/T | 8.42212e-05 | 0.00648872 | missense | SORBS1 | GRCh38.p7 | 10:95357785 | CCTCTTCACTGCATG[G/T]AAGTTGGAAGAATAT | 10580 |
rs556073659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534278 | CCAGCTAATTTTTGT[A/G]TTTTTAGCAGAGACA | 10580 |
rs556073798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526035 | ACAGCTACCATCAAT[A/C]AGTTCAGTCCTCCTT | 10580 |
rs556093279 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458415 | AATCTAAGGTTTCTT[A/G]ACATTTATATAGGTC | 10580 |
rs556116435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398654 | TTACCCTGGACCAGG[A/G]ATTTCTCAACATGCT | 10580 |
rs556152156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541662 | CCAACATGCCCAACC[C/T]CCAGAAACCAGTCTT | 10580 |
rs556188297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543186 | TCTGGTTGGATTCCA[A/G]CTCACCCCCCAACCC | 10580 |
rs556189509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525551 | AGCAAATGTCCTGTC[C/G]TGTTTTTGCACAAAT | 10580 |
rs556192093 | snp | C/T | 3.32276e-05 | 0.00407586 | missense | SORBS1 | GRCh38.p7 | 10:95421962 | GGGCACATGCCTACC[C/T]GGGACTTGTCAGAAG | 10580 |
rs556200928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407411 | AAGTGAATGTATTCC[A/T]CTTAAAAGATCATGT | 10580 |
rs556217893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528711 | ATCACCTGAGGTCAG[A/G]AGTTCCAGACCAGCC | 10580 |
rs556222500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521229 | AGTCGCCAATGGCCA[C/T]GATAGGTTAAGAATG | 10580 |
rs556232539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384983 | CTGCAAAGGTACTAC[C/T]CGGAGTGAGTATCTA | 10580 |
rs556242359 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394089 | ATTTTCAAGAAATGT[A/C]ATCTCCCACTATGAC | 10580 |
rs556244424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401079 | TTCAAGAGGTCAAAG[A/G]ATTAGGGACAAAAAG | 10580 |
rs556246546 | in-del | -/AA | 0.451109 | 0.148509 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479402 | TCATCTTCTTACTTT[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs556250193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386477 | CCCGTCTCTATTAAA[A/C]ATACAAAAATTAGCC | 10580 |
rs556263502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428530 | TAAGGTGGAGTAATT[C/T]GTCCATACCGCAAAG | 10580 |
rs556267836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337656 | TTGGAAGCTCCCCAT[C/T]CCAGCCAACCCAGCC | 10580 |
rs556268393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484851 | ATGGTGGCGCACACC[A/T]GCAGTCCCAGTTACT | 10580 |
rs556282364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456641 | TGTAGAGGTGGGGCC[C/T]TGGGGCAGAGAGAGC | 10580 |
rs556286823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535219 | GATGAAGAAGAGACC[A/T]CTTCATCCAAAGTGC | 10580 |
rs556295157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338857 | GGGACTACAGGCGCC[A/C]GCCACCACGCCTGGC | 10580 |
rs556304505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408194 | CACTGGTATGCCTAG[A/C]AAGCTTGCTGAAAAT | 10580 |
rs556319882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324927 | AGGCTGCTGTGGACT[A/G]TGACTAACTGGGATA | 10580 |
rs556326498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429236 | GCATGATCTCACTCA[C/T]TGCAACTTTCACCTC | 10580 |
rs556332074 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468639 | TCTTTTATTATTAAT[A/G]TATTTATTTGCCTAA | 10580 |
rs556336395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95416170 | GAGGGAGAGGAGGGC[A/G]TGGGGGAGAGAGAAC | 10580 |
rs556344975 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476779 | CGACATCCCTCACAG[A/T]GATTTTTCTCCTTAA | 10580 |
rs556345839 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358366 | AGAAAAATCAGTGAC[C/T]AAGTGAAATTGGAAC | 10580 |
rs556354608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529170 | GGGAAGCCAGTCATA[C/T]ACTCCAAAGCCAGAG | 10580 |
rs556359930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515105 | CAGACTGAAAAGCAG[A/G]TCCAATTCTCTTGGA | 10580 |
rs556361054 | snp | A/G | | | stop-gained | SORBS1 | GRCh38.p7 | 10:95354905 | CATCATGACGTCTTC[A/G]AATAAATTCTTCCGT | 10580 |
rs556376507 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433787 | TGTATTGAACGCAAT[A/G]CACGAAACGCACAAT | 10580 |
rs556413820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449440 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTTGAA | 10580 |
rs556415077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426338 | TTTATCCAAAAAGAG[A/G]TCTGGCCTTGGCCCT | 10580 |
rs556419011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463550 | GCATTAAAAGGAAAA[C/T]ACCAGTTTAAAGTAA | 10580 |
rs556430783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436141 | GTCTCACCAAGGAGA[C/G]AGTGGGACTCACTCC | 10580 |
rs556441578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415078 | CCGCTTTTCATCCAT[C/G]TATTTTTGAATCCTT | 10580 |
rs556449303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464612 | GACAGGTCCCGTATC[A/G]TTTATTCTTCTCCAA | 10580 |
rs556450858 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525276 | CAATCTTCAAAGGCA[C/T]TAAAAGTAGGACAGC | 10580 |
rs556452487 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484225 | AGACTCCATTTCAAC[-/AA]AAAAAAAAAGGTTGT | 10580 |
rs556453247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380870 | TTAATAAAAACCAAA[C/T]TCCAGCATAATAATT | 10580 |
rs556467703 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329474 | GGCCTCTGAAAGTGT[C/T]AGGATTACAGGTGTG | 10580 |
rs556470039 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362157 | ACTCACTGGAAGAGT[A/G]AAGTGAGAGAACAGA | 10580 |
rs556472652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482627 | TCGTGTTTATTACTG[A/G]CAGCCATGAGAAATA | 10580 |
rs556479775 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562453 | CAGAGACAGGGATCA[G/T]AGTGGGGAATCTGCT | 10580 |
rs556485734 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451815 | GGCCATAGTCCACAA[C/T]ATAGGTAAACGAGAT | 10580 |
rs556505066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494005 | TCCAGATCTTTAGGG[G/T]AGTAGCACATCCCTG | 10580 |
rs556525613 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542416 | TGGGTGGCCTCAAGC[G/T]GCCTACATCCAAATG | 10580 |
rs556528335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548061 | AGGGGAGAAGAAATG[C/T]ATGGGGACAGGGGAA | 10580 |
rs556529835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549641 | TAAAATTTCTAGTTA[C/T]TAGTCCTGGCACATA | 10580 |
rs556549789 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386736 | AACAATGTATGTACT[G/T]TGAAAAGGAGAGGGA | 10580 |
rs556560784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444519 | ATACATAAATAGCAA[C/G]TACATTATTGTAAAC | 10580 |
rs556570531 | in-del | -/AAAAAAAAAAAA | 0.240765 | 0.249829 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407946 | GTGAGACCTTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 10580 |
rs556606365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317995 | ACCACTGCACTCTAG[C/T]CTGGGCAACAGAGTG | 10580 |
rs556609999 | in-del | -/CACA | 0.0158469 | 0.0875917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358669 | TAACACACTGTCATT[-/CACA]CACACACACACAGAC | 10580 |
rs556610780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430824 | CCTTTCCAGCGGGTC[A/G]GGAGTCAGGGCTGGG | 10580 |
rs556640930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459128 | AAAGTACAAAAATAA[A/G]TAAGCTTTTTCTTCT | 10580 |
rs556645669 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545262 | CCACTCCTGCCTCAC[C/T]TCTCCACCCAGATTC | 10580 |
rs556652663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477947 | ATTTGTGCTGGGCCA[C/T]ATTCAAAGCTGTCCT | 10580 |
rs556655479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510482 | GCACCTGCCACCATG[C/T]CCAGCTAATTTTTGT | 10580 |
rs556660197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535820 | ATGAAATTTTTCAAT[A/G]TATACATTTTTATAG | 10580 |
rs556665773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550187 | CTGAACTAAGCCAGG[A/G]GAAAGACATATAAAC | 10580 |
rs556702438 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335472 | ATCTTCAGGAACTCA[A/G]TCTGGGTCTAAGGAA | 10580 |
rs556706264 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359906 | AGGGGACTGCCGAGG[G/T]TGGGGGTCAGAGCTC | 10580 |
rs556707154 | in-del | -/A | 0.395453 | 0.203331 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465528 | GTGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10580 |
rs556722758 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403167 | TCCATCTCCCCAAGG[C/G]GACTGAGAGGTACCT | 10580 |
rs556735727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552630 | GGAAATGGCTTTCGA[A/C]TTCAAATTCTAGATG | 10580 |
rs556740350 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394892 | ATTTTCACCAGCCAA[A/T]AATGACTATGAAAAT | 10580 |
rs556745027 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325569 | CTTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTG | 10580 |
rs556748332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465067 | AGTCACAGATAGCTA[C/G]CTTTGCCTTCCTACA | 10580 |
rs556774371 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554373 | TGTCTTTCAAAACTC[C/T]GTGCGGGGTGGGGGT | 10580 |
rs556789755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471158 | TTCACCACTGTGCCC[C/G]CAATTCTGATTTTGC | 10580 |
rs556791022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430191 | GGGCCGGGCATGGTG[C/G]CTTACACCTGTAATC | 10580 |
rs556791314 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508489 | TATTACCTCATTTTA[C/T]ACCACTTATGTCAGA | 10580 |
rs556805670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380293 | CCAGGGAAAGGAGCT[A/G]GAAACAAAGGAGAAA | 10580 |
rs556808300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543248 | AACATATTGTTCATC[A/G]CACTTTGGCATAAAA | 10580 |
rs556809910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365107 | GATGTTATTCGATAC[C/G]TGTGCTCCTTTATCC | 10580 |
rs556829972 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563296 | ATAGCTACAAAAAAT[A/G]AAGAGGTTTATTGAC | 10580 |
rs556846874 | snp | C/T | 3.58198e-05 | 0.00423186 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339366 | GTCCTTGTCCTAGCA[C/T]GCCTCTGCATGCCTG | 10580 |
rs556854318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331994 | CTACAGATGTAATCA[C/T]GTATCATGACCTATG | 10580 |
rs556878817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359445 | CTTACTATGTTGCCC[A/T]GGCTGGTCTTGAACT | 10580 |
rs556880852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445735 | AACCTTAAGTGCTCA[C/G]AGCCTGGGCAGTGAG | 10580 |
rs556916066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354164 | TATCCCAGCAGAAGC[G/T]TGTGATTTTGCCCAT | 10580 |
rs556921729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450653 | ACTACACGCACACAC[C/T]ACCACGCCTGGCTAA | 10580 |
rs556929908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473521 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10580 |
rs556937308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495851 | GGGAGAAAATGCCCA[A/G]CTGGCCCTGAGGCTG | 10580 |
rs556949984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367250 | CAGGGTCTATGTTGC[C/T]CAGGCTGGTCTTGAA | 10580 |
rs556971553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502311 | TGAATTGCCACATTT[C/T]CCCACTAAATTCAAA | 10580 |
rs556995014 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342514 | ACAGCTCATTGCAGC[C/T]TCAACCGCCTGGGTG | 10580 |
rs557014400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457996 | ACCCCTAAGTCTATA[A/G]AAGAATAAAATATCC | 10580 |
rs557025191 | snp | A/G | 0.0020899 | 0.0322581 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414367 | GGGGACACGGCTCCA[A/G]TCATCACACAGGCAC | 10580 |
rs557046921 | in-del | -/AGAA | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373974 | AGAAGCAGTCTCATT[-/AGAA]GAACTCTGAGGCCTG | 10580 |
rs557059279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327039 | TTACATTATATTTCT[A/G]CTAGACAATGCCTCT | 10580 |
rs557064808 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474059 | TAGAGATTCTGAAAT[C/G]CTTAGAAAAAAAAAC | 10580 |
rs557067915 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313862 | GTGACCAAGCAGCCC[A/G]GGCGTCACAGGGGCC | 10580 |
rs557081938 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394013 | TGACTGTCTTCCCCA[A/G]CAGGTACAAATTCCT | 10580 |
rs557091604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365613 | TGAAGGCCCGGCTCA[A/G]TTGGAAGCTCTTTAA | 10580 |
rs557129490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431641 | CTTCCTCACAATAAT[C/T]CTGAGGCAGATGCAA | 10580 |
rs557147553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558186 | CCCAGCTACTCGGGA[G/T]GCTGAGGTAGGAGGA | 10580 |
rs557159246 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383280 | AAATTAACCGTGAGT[A/G]GTGTGTGCACCTGCA | 10580 |
rs557161136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388728 | GGGATTTACACAGGG[C/T]AAACAACTCACTTAG | 10580 |
rs557163949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382223 | GTTCAAATCCTGCCA[C/T]ACCCCTTGCTAACTA | 10580 |
rs557170983 | snp | C/T | 3.30256e-05 | 0.00406346 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397170 | TTCAGGCCCACAAAA[C/T]GTGTATTGGCACATA | 10580 |
rs557193276 | snp | C/T | | | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95422212 | AGAAGGCTCTGGCTC[C/T]AGACCTACACGTGGT | 10580 |
rs557212853 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334437 | CCACAGCCTGTGCAC[A/T]CCCATGGAGAAGGGG | 10580 |
rs557218196 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423155 | GTATCATCTCTTGTC[C/T]CTACTCTCTGTCCTT | 10580 |
rs557243987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480159 | CTGAAGCAAAAGACA[A/C]TGAATACTTGAAACC | 10580 |
rs557270549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438275 | GGGTTTCCTGATACA[G/T]ATATATATTCTATTT | 10580 |
rs557273449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523855 | ATGTATTTGGCAAAA[A/G]CAACACCAAAATGTT | 10580 |
rs557280799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517644 | TACTTTGTCCTGTGC[A/C]TGGAACACAGTAGGT | 10580 |
rs557290965 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391741 | GAAAAAAGAAGGTTG[C/T]TAAGCCAGCATAAAC | 10580 |
rs557296585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355754 | CGTGGGTCTCTCCTG[A/G]GAGGGCTCTGAGCTG | 10580 |
rs557301628 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464515 | GCACCTGGCAGAGTC[-/G]GGGGATGGTGCAAGT | 10580 |
rs557304737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511963 | AAAAATCAGGTCACC[C/T]CCATCCTACACATAC | 10580 |
rs557336671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530272 | CACAACCAGGTGTTC[C/T]TTCCTACCTCTCCCA | 10580 |
rs557364386 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460340 | CAGATACATTATGTG[A/C]GATCACTTTTAAACT | 10580 |
rs557381303 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497574 | CCCCTCGAACCATAT[C/T]TCCAATACCCCACTT | 10580 |
rs557385082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412106 | CACTTTTCCTAATTT[A/G]TCTCCAAAGTGATAT | 10580 |
rs557390140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426718 | CAGACTCCAGCCTAC[A/G]TGCATCTTCTCTTGC | 10580 |
rs557415544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374528 | TGGTCTGTTTTGGGG[A/G]TGGGGAGACAACTAC | 10580 |
rs557423828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511294 | GCTGCAGCCTCAACA[C/T]CCCAGGCTCAAGGGA | 10580 |
rs557426252 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537366 | AGACACACAGTGACA[C/T]GCTGGAGAAGCCACC | 10580 |
rs557435252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397760 | AACTCGTTATAGCAT[C/T]CACTGCCAGAGTTTT | 10580 |
rs557463031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433858 | TCCAACTCTATCAAG[A/C]GGCTAAGCGACTGAT | 10580 |
rs557463358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550800 | AAAAGGACAGTAGAC[C/G]GATGCATTTCTTAAT | 10580 |
rs557465340 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539167 | AAGTTCCTCAGATGG[A/G]ACCTTCCACTAGCAC | 10580 |
rs557465369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425275 | TCTATTCAAGTGACA[C/T]TAGCAAACAGCTATG | 10580 |
rs557478458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433338 | ATAACAGACCCAGGT[C/T]AACTTTTAGAGTTTC | 10580 |
rs557500131 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517904 | ATCCTCTTCCAATGG[A/G]TGCACATGCCCCAGG | 10580 |
rs557522220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408276 | TAACAAGACTCTCAG[G/T]ATCCGACGCACATAG | 10580 |
rs557524586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425947 | TGGGGGGAGTGCCTC[A/G]GAAAGTTGGATCCTA | 10580 |
rs557529129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420995 | AGTTTTTGAGCAGCA[A/C]AGCTTCCTTTAAGAG | 10580 |
rs557550856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518901 | AGTCTTCCATGGGCT[C/T]ACACCCATCAGCAGT | 10580 |
rs557581120 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313237 | CTTTCCTGAGAACAG[G/T]ATTTGAAAGAACAAT | 10580 |
rs557588174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482448 | CCTGAGAGCTCTAGT[C/T]ATCAGAAATATTCTG | 10580 |
rs557597622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551290 | TATCAAACAGACTAA[C/T]ACCTAGCCCCTTTCC | 10580 |
rs557601893 | snp | C/G | 0.00163594 | 0.0285533 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337065 | TGGGGGAGGCTGAGA[C/G]ACAGGGAGGGACTGG | 10580 |
rs557605584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446435 | AATATGGGTTGGTTA[C/T]TGGGAAAGGAAAGAA | 10580 |
rs557610671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532855 | TGCAGGCTAGACAAC[G/T]CCATCTTGAATGTTA | 10580 |
rs557622760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384436 | CCAGAAGCTACACCA[C/T]GGCAGAGCACGTTTG | 10580 |
rs557627445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452616 | AACATAATATCAAGC[A/T]CACAGCAAAAATTCA | 10580 |
rs557646826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419394 | GGCTAGCACGCACCA[A/C]AGGGACTGGCGGGTA | 10580 |
rs557647669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322305 | CAGGTTAAAAAAATA[G/T]ATATTCCAGTAGTGG | 10580 |
rs557650129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404567 | AGGAGTCCATTAACA[A/C]AGAAAAGTTACACAC | 10580 |
rs557665728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420432 | GTTTCTTGATCTGCA[C/T]AGAGCTGATGGCATC | 10580 |
rs557670291 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429911 | GCAGCACCTGGCACA[C/T]AGATAATGCTGAATG | 10580 |
rs557685991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447728 | GCAGAAGGCTCTTCA[G/T]AAAGCCAGAAAGGAT | 10580 |
rs557691397 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312603 | CTTGTTTCGTCATAC[A/G]TAGGAAGGCGACGTG | 10580 |
rs557725130 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361215 | CATCTCTGCTCTACC[A/T]CACCAACAGTCAGAT | 10580 |
rs557732502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545181 | TACTCTCATTTCTGT[A/C]CCTGTTGGGATTTTG | 10580 |
rs557735807 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552334 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10580 |
rs557740312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427586 | GTCTGGAGAATGAGT[A/G]TTAACTGGGCAATTT | 10580 |
rs557742108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553039 | AGGCAATGTAGTGAA[A/G]CCCCATCTCTACCAA | 10580 |
rs557753175 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419498 | TCAAATGTCCCATAT[A/G]TGATTTCTTCTTGTC | 10580 |
rs557754096 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531933 | AGGCAAAGTCAACTT[A/G]GAGGGGAAAACACAG | 10580 |
rs557756510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377146 | AAAAACATTGATAAT[C/T]GCAAAAAGAGAGTTG | 10580 |
rs557770847 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530550 | GATGTGCTCTGCTGG[A/G]GTAAAGAAATACTTT | 10580 |
rs557784317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489655 | AATACATAAGTGTCC[G/T]GCTACCTGATGCCAT | 10580 |
rs557786734 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334788 | CCTGTGTCAGAAACG[C/T]TTAATTCTTTTCAAC | 10580 |
rs557799312 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311541 | TACGAACATATTTTA[C/G]AAATAATGGCAAAAT | 10580 |
rs557809390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328561 | CAGTTGGGGGGTAAT[C/G]GCAGATACATATTCA | 10580 |
rs557814687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540818 | TCCCTACCTTGAGAA[C/T]TTCCTTTCTGCAAAT | 10580 |
rs557815105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533376 | CACCAGAGAGTAATA[C/T]GCATTTTTAACAAGC | 10580 |
rs557830430 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509081 | GATTGTAGCAGCCCT[C/T]CTGGAAAAGGAGCAC | 10580 |
rs557836993 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315002 | CAACTAAAAAGATCG[C/G]TTCATGAATGATGCT | 10580 |
rs557842312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398753 | GAAAAGTTCTACAGC[A/G]GAGAAATCTCTCTGA | 10580 |
rs557844912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474957 | AAGCCTGAGCTTCCC[A/G]CAAATGACATGGCTC | 10580 |
rs557889441 | snp | C/T | 5.08126e-05 | 0.00504021 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351172 | TAGGCAAATATTGCT[C/T]TGGGTCAAGCAGCAG | 10580 |
rs557892651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512964 | GCGAAGTAGTGGACC[A/G]GTTCTCATCGAAGAG | 10580 |
rs557894803 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433525 | TTTGTTTTGTTTTCA[A/G]ATTGCTCACAGCCTA | 10580 |
rs557913822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329087 | CTCTGCCAGAGGAAG[A/G]TATCAGAAGAGCTAG | 10580 |
rs557971927 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514132 | AAAAGAAACATCTGA[A/G]GGGAAAAAATACATC | 10580 |
rs557984248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406656 | TTCTTTCCCATTGTA[C/T]AGAGGAGGAAACGAA | 10580 |
rs557996254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369831 | CTGGTTCCTTCACCC[A/T]AATTGGAAACTCAGC | 10580 |
rs558009006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357044 | CGCATTGCTAGTGTT[A/G]AACGTTCGGCTATGG | 10580 |
rs558021930 | in-del | -/TAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461343 | TGTATTCTCTGGATT[-/TAAAAA]TAAGTATCTTAAATT | 10580 |
rs558026352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526991 | TCTTGTTTACTCGTA[C/T]TCCTCCTGAACCTAA | 10580 |
rs558037377 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336222 | GCATACATGGGATGT[G/T]AGGAAGGTCTGCCTT | 10580 |
rs558054917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345334 | GGATTTGAACACAGG[G/T]CTTCCTGACTCTAAA | 10580 |
rs558067518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428316 | ACTTGGGAGGCTGAG[G/T]CAAGAGAATTGCTTG | 10580 |
rs558068880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435130 | TGGGCTCCAGATGAG[C/T]GGAAGAACGAAGGAA | 10580 |
rs558070769 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442573 | GCCTGCTCCCCCTTC[G/T]CCTTCCACCATGATG | 10580 |
rs558079130 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344711 | CGCCTGGCCCCGACA[A/G]CATGCTTTTTTGAGT | 10580 |
rs558081033 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469684 | CATCCTGCATCATAA[A/G]TGTTCATAAAATACC | 10580 |
rs558087629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534318 | TGTGCTGGCCAAGCC[A/G]GTCTCAAATGCCTGA | 10580 |
rs558088101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455675 | TGTGGCAGCTCATGC[C/T]TGTAATCCCAGCACT | 10580 |
rs558108762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407219 | CTGGCTGAACATGCA[G/T]AAGCCCAGTGCAGCT | 10580 |
rs558143361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553771 | TGTAAGCAGGTAACA[A/G]TAAATATGATAGTAA | 10580 |
rs558154210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498967 | GGTTTTGATGTCATA[C/T]TATACCTACATAAAA | 10580 |
rs558158738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464563 | TGTCACTCAGGGTGC[A/T]CGCTGTCTAGCCCAC | 10580 |
rs558165870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514263 | AGTCATCTTCTGCCA[C/T]GACTGATGCCAGCTA | 10580 |
rs558189777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476392 | AGCCTTTCAACTCCC[A/G]AGGTAGGTTTGGCCC | 10580 |
rs558198414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322969 | ACAACAACAGGGTGG[A/G]TGCACAGAAGAAAAT | 10580 |
rs558203538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338591 | TCTTTCCCTAGTCAC[C/G]TTATTCCCAGAGCAA | 10580 |
rs558237134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536934 | TCCAATCCCTCTAAC[A/G]GCTTGAATTCAAGAT | 10580 |
rs558263333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561013 | CCAAAAAAGGAAATT[A/T]AAAAACCCCCAACCC | 10580 |
rs558267354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423752 | TTTAGTTTTAGTTCA[A/G]TGTACACAACAACTC | 10580 |
rs558277849 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334796 | AGAAACGTTTAATTC[G/T]TTTCAACTAGCCACT | 10580 |
rs558321580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363450 | GAAAAAGCGTTTGCT[A/C]GTCTACCATCACCAT | 10580 |
rs558391157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351662 | CCCGGCTCAGCCCAA[A/G]GCCTCTTGCTTCTGG | 10580 |
rs558408561 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358406 | TATGGGCTCTTAGTA[C/T]CACAGCCACATTTGC | 10580 |
rs558417796 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464188 | GCCAGGCAAGGTGGC[A/G]CGTGCCTGTAATCTC | 10580 |
rs558421846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527583 | CAACTATACACCCCA[A/G]GACAATGTATAGTTG | 10580 |
rs558439488 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494249 | GCAGATCTGAGCCTT[C/T]ATACACCTGTGTGGG | 10580 |
rs558444322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494519 | TAAATGCCGTGTACC[A/G]CAAAGATGACAGACG | 10580 |
rs558448079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484769 | GCTTGAGCCTAGGAG[C/T]TCAAGACCAGCCTAG | 10580 |
rs558452448 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447492 | AAAAAAAAAATCTAA[C/T]CTGGGACTTGATTTT | 10580 |
rs558462308 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358731 | GCGCGCGCACACACA[C/T]ACACACACACACACA | 10580 |
rs558482837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371494 | GAGAAAGAATGGAAG[A/G]TTACGTTTGAAAAAA | 10580 |
rs558489830 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485414 | GCTGAATTATCCAAA[A/G]TTCAACAAGCACAAA | 10580 |
rs558490178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393170 | ATAGACTCTTCTTGG[A/C]CTTGAGGAAGACACT | 10580 |
rs558491787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450602 | TGCCTCCTGGGTTCA[A/G]GCGATCCTCCTGCCT | 10580 |
rs558498696 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339045 | CAGTGCTCAAAAACC[A/T]CCCCAGAGAGGCTGT | 10580 |
rs558509947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401979 | TCCCACCTGGAAAGG[C/G]CTTCTGTTGAATGTG | 10580 |
rs558513312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486783 | AACATAACACACAAA[A/G]AAATTTTAAGTAGCT | 10580 |
rs558520874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324304 | CTGATGCTCAGAGGG[A/G]TTTCATGCATTCCTC | 10580 |
rs558539057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324691 | TCCACTCACTGCCTC[C/T]GGATTAAGGTGTCCG | 10580 |
rs558544148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522066 | GGTGTCTGGAAAAAG[A/G]ATGAAGACACATCAC | 10580 |
rs558555789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535900 | ATAATCTTTTAATGG[A/C]AAGGAAAAGGCAAAA | 10580 |
rs558574636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485889 | TTTAAAAAGTACAAA[C/T]GCAAATGTGTAAATC | 10580 |
rs558575896 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415190 | CTTGGGAGTAAATAC[A/C]ATTTCTTTGGCACCT | 10580 |
rs558576446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494860 | CAATTTTTATTTTTA[C/T]TTATTTATTTATTTA | 10580 |
rs558585171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502060 | CACAGACAGAAGAAA[A/G]CACTCTCTTTATCTA | 10580 |
rs558618544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523066 | AATAATGTCACTTAC[C/T]TCTCAAACCATTACC | 10580 |
rs558628640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386830 | TAAAGCTCCTTTCTT[A/G]GACGGGCCTGGTGGC | 10580 |
rs558655742 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561840 | CTTCGTAAAATCTAG[G/T]GAAGATTAACATAGT | 10580 |
rs558658651 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542298 | TGTTCCTTACTCATA[G/T]CTGGGCCTCCCACAA | 10580 |
rs558666437 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95349704 | TTCGAACTCCTGGCC[A/G]TAAGTGATCCTACTG | 10580 |
rs558667250 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520315 | ACGAAACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs558681231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515851 | CTATCCAAATTTGGC[C/T]TAACGCACCCTATGA | 10580 |
rs558690020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501189 | TATACACATTTCCCA[C/G]AAGCATCTCAGAACA | 10580 |
rs558694964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516876 | GCCAAAAGTTCATTT[G/T]CAAGTTGGAGGGTTG | 10580 |
rs558715566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417720 | TCCGCCTCCCAGGTT[C/T]AAGCAATTCTCCTGC | 10580 |
rs558720420 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520446 | GACCAGCCTGGCTAA[C/T]ATGGTGAAACCCCAT | 10580 |
rs558742970 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366362 | CCACAGAGGTACTAA[C/T]GTGAGCCTGGGTACA | 10580 |
rs558755629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394764 | TTTCGAATGACTGAT[G/T]ACCTATTTTAGTGTT | 10580 |
rs558758571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523644 | ACTTGATTATCAAGG[A/G]TCACCTGTTCTATTG | 10580 |
rs558759569 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515575 | CAACTAAGAAAGAGA[C/T]TTAAGCAGAAATCAC | 10580 |
rs558791241 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541187 | CCGTAAAGGCAGTGA[C/G]TCCTGCTGACAATGA | 10580 |
rs558806005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443408 | TTGCAGTGAGCCAAG[C/T]TCGTGTGTGCCACTG | 10580 |
rs558826274 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487483 | AAAAGCTTTGAGGGC[-/A]GGGGGATTGGGGGGT | 10580 |
rs558840622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408305 | AGACTGAGAAGCCCT[A/G]AGCAAGGGGACCCAC | 10580 |
rs558840922 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316714 | TGAGCTGTGCTGTAA[C/T]TATAAAATACACATT | 10580 |
rs558848111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417059 | GCCCCAGAGGTAAAT[C/G]ATCAGCCTCAGATTC | 10580 |
rs558880546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326220 | TCATTTCTCTTCTTG[A/G]ATACTTTTTACTCTA | 10580 |
rs558882773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472807 | GCCAAGGTGGGCGGA[C/T]CACTTGAGGTCAGAA | 10580 |
rs558896472 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322623 | TACTACAATAGCCAC[A/G]GAATTCTTATAAATA | 10580 |
rs558901199 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366332 | ATGTCAGGTATACAG[A/C]AACAGAAGTAAGGAC | 10580 |
rs558910996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430933 | ACAAAGAAGCCCTCA[C/T]GGGGACCAACATCAC | 10580 |
rs558937888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542490 | GTCAAATGACCTCTT[A/G]TCATTCTTCCAAAAT | 10580 |
rs558941808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549275 | ATCTAATTAATTTCA[A/G]TAGCCACATGTGGCT | 10580 |
rs558951151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431478 | TGTGCCTGATCTCAA[A/G]GTCAGCATTTGCCAA | 10580 |
rs558961282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466956 | ATATTGGAATATCAC[A/G]TTGTTCAAACTAACA | 10580 |
rs558970550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346222 | CACCCACTCCATAAG[G/T]AATTAACATAAGCAA | 10580 |
rs559035286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479157 | GAAATGAGTAGATGC[A/C]AAGCAGAGAATATAG | 10580 |
rs559052096 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563356 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTCT | 10580 |
rs559070482 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537051 | CCCAGCATGCCTTGG[G/T]CTTCACTGTCTCTGT | 10580 |
rs559075250 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444291 | ATTTTGTGGAGATGG[G/T]GTCTCTCTATTGCCC | 10580 |
rs559096749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465963 | TCAGCCTGACGAACA[C/T]AGTGAAACCCCATAT | 10580 |
rs559109045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326523 | TTCTATTAGTTAAGA[C/T]TCAATTTCTCTCTGT | 10580 |
rs559112823 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474704 | TTCTTTGCTCATATA[A/G]GATAATATTTATGTT | 10580 |
rs559132575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437420 | AGATGGGATGGCCCC[G/T]GCCTGACATACTCCG | 10580 |
rs559135752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480243 | TACCCTGCCCAAAGA[C/T]AAACTAGGACAAACC | 10580 |
rs559139619 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555913 | AAACAGAGAAAACAA[C/T]GATGCTAATTCTTCC | 10580 |
rs559142975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339459 | CCTTCCCTGCTGAAC[A/C]TGGAGGGAATTAACA | 10580 |
rs559146060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402276 | GAGAGCCCCTGAAGA[A/G]AAAGTGTCACTTTAC | 10580 |
rs559174343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550230 | ACTCAGTGTGGCCCA[G/T]GCCAAAACAAACATA | 10580 |
rs559185049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466238 | CGACGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 10580 |
rs559206330 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386565 | TGCTTGAACCCCAGA[A/G]GCAGAGGTTGGGGTG | 10580 |
rs559211326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325616 | TGTTGCCCAGGCGCA[A/G]TCTGGGCTCACTGCA | 10580 |
rs559217765 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347289 | TCCCTCAGTTCAAAT[A/C]TCAATTCCTGCCATA | 10580 |
rs559225479 | in-del | -/AAGTT | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361990 | AGTACTTAACAAAAC[-/AAGTT]AAGTTCAGAAGCTCA | 10580 |
rs559237737 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443178 | AAACGTAGAAGCGGC[C/T]GGGTGTGGTGAGTCA | 10580 |
rs559252888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374724 | AGAAAGGAGAAGAAA[G/T]GAGGTGTGCACCAAT | 10580 |
rs559268004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332742 | ACAGGTGTAAGCCAC[C/T]ATGTCTGGCTTGCCT | 10580 |
rs559287201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418118 | AGTCTCACCCTGTTG[C/T]GCAGGCTAGAGTGCA | 10580 |
rs559316999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366682 | CACCTCCCTCCCCCC[A/G]TCTATTTTTTTTTTT | 10580 |
rs559344901 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557783 | AGAAGAGCTCAGCTG[A/T]TTCAGAGACAATAGA | 10580 |
rs559345527 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480717 | CAGCAAGCATTTCAT[-/G]AACACATTCTGCATG | 10580 |
rs559351745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472234 | AACTATGAATGGAGC[A/G]GCAGCGGTTGGGGTT | 10580 |
rs559357510 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398304 | TGGAACATATTGCAG[G/T]CAATGGTCTAGTAGA | 10580 |
rs559373190 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513219 | ACAGGGATGTGGGGC[A/G]CATGTAACCCAGATG | 10580 |
rs559376705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388035 | CCCAGGCTGGAGTGC[A/G]GTGGTGCGATCTTGG | 10580 |
rs559393557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346607 | TTTGTCTGACCTTAG[C/T]AGAACACTAGATAAA | 10580 |
rs559412118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479457 | CGCTAAGGGAAACAA[C/T]ATTGCAGAGCTCCTT | 10580 |
rs559420983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459973 | CTTCTGATCCTGCCT[A/G]GAAACAAAGTGTGGT | 10580 |
rs559429597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425492 | ACTAAATGAAAGTAT[G/T]TGGCATAAAGCATGT | 10580 |
rs559430027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495239 | CAGTACTGTTATATT[A/C]TGGCCTAAAACAAGA | 10580 |
rs559436306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381178 | ATGAAATTTGTCCTC[A/G]ATATTGCACTTGTCA | 10580 |
rs559438177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388847 | CAGCCACTCTCCTAC[A/T]ACTGCCAGGAGCCAC | 10580 |
rs559446713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529647 | CCATGCCTTTCAAAG[G/T]TAGGTGGTCCCTAGA | 10580 |
rs559455994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504311 | GCATAGACACTTAGA[A/T]ACCCACACACAGACT | 10580 |
rs559487063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354203 | TATGAAGAACTTCCT[C/T]TTCCCAAATCCCCAA | 10580 |
rs559496489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481147 | CTATATGGCCACATC[A/G]GGGTCAGAAACAGCT | 10580 |
rs559502512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382687 | TCTATATGTCTGTTT[C/T]TATGCTAGTACCAAG | 10580 |
rs559505725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488059 | CTTAGTGAACCCTCA[A/G]TGAACTTTTGGATGA | 10580 |
rs559511990 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413736 | AGCTTTTTCTCTAAG[C/G]AGTTGGGCTTTCCCG | 10580 |
rs559515264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446141 | CTTGGGTGTGCCAGC[A/G]GGGAGTCAAACCGCC | 10580 |
rs559542030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517103 | AGCCTCAGTTTCTTC[A/G]CCTGGGAATCCTAAT | 10580 |
rs559557116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341104 | CCTCGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 10580 |
rs559559545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489146 | CCAAGCTTATCCTAC[A/G]TCAAAGGCCTTTCTT | 10580 |
rs559568119 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488681 | CTCTTTGCTCCTTAT[C/G]TCAGTGAACGGCAAC | 10580 |
rs559584133 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340152 | AGTAACTTTAGCAAG[C/T]CAGAGAATTTTGCCA | 10580 |
rs559597221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496466 | TCCCATTGCCCAGCT[A/G]TCCTCCTCCTGCATC | 10580 |
rs559606274 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524184 | TTTGGGAACATTTCG[-/A]AAAAAAATGTGAATG | 10580 |
rs559625345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347185 | ACATTCTCTTCACTC[C/T]AATCTGTCACCCAGG | 10580 |
rs559632508 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95481863 | CCAGGAACACAGTCT[A/G]GAATTCAGCCAAGAA | 10580 |
rs559670411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512286 | AGCCAGGCATGGTGG[C/T]GCATACATGTAGTCC | 10580 |
rs559672483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519137 | TCCTAGGATGAAAAG[G/T]CTGTGAAACAGAATA | 10580 |
rs559676038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510965 | CATTTATCTCGTTCC[A/G]TGCAAGCCTGTCTTT | 10580 |
rs559678079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517714 | GGCAGGGAAGAGGAC[A/G]TTGTGCACAGCTGAC | 10580 |
rs559680947 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396553 | GTTGCCCAAGCTGGA[A/G]TGCAATGGCGCAATC | 10580 |
rs559691003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377255 | CACTACTTCTGGGCT[A/G]TAACACCTGAGGGAG | 10580 |
rs559697972 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320174 | TCTTGCCAATCCTGG[C/T]GCCCCACGCTCAGCC | 10580 |
rs559722379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412480 | CACCTCTGTTACCCA[A/G]GGCCAAACCCGAAGC | 10580 |
rs559722922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503464 | GTAAATAGAGAGGGG[C/T]ATTTCCCAGGTCTCT | 10580 |
rs559730074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518437 | TAGTGTGGAATCTTC[C/T]ACTACTATGTGACCC | 10580 |
rs559745447 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537147 | CCCCTTATCCATCTA[A/G]GTAGGTCTAAATCTC | 10580 |
rs559749169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474395 | ATTTTTAAGCTACTA[C/T]AATTAGTCTCCATTT | 10580 |
rs559761625 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367374 | ACTTAGACAAATAAA[C/T]TCCCATTCTAAAGGT | 10580 |
rs559763253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418773 | GGTGAAAAATATTTA[A/C]AAGTTTTATAGGTTG | 10580 |
rs559781113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404702 | AGTGAACCCACAGAG[C/T]GCCGCCTGGTAACAG | 10580 |
rs559782083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525085 | AGATTCAAATGACCT[C/T]AACAGCCCAGCATTC | 10580 |
rs559806492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513047 | TTCAAACCTGTGTGT[C/G]GGCTGATTCTCCGAA | 10580 |
rs559815122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511435 | GCCCAAGCTGGTCTC[A/G]AACTCCTGGCCTTAA | 10580 |
rs559818406 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559718 | AGAGCTTGGTTGGCA[A/T]GGGGCTATTTAAGGC | 10580 |
rs559822789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376473 | CACCAAACATTTAGC[C/T]ATCTATGCCAGTTGA | 10580 |
rs559856384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411192 | AGTACACTGTACAGA[A/G]AAATGTAAGACAATG | 10580 |
rs559858216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538090 | ACACTGTAGCCTGGG[A/G]GACAGAGTGAGACTT | 10580 |
rs559858342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545353 | TTACCTCATCCCTGG[C/G]TTCTAGACTCTGCCC | 10580 |
rs559881101 | in-del | -/G | 0.4941 | 0.0539917 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560085 | CGCGGGGGGCTGGGC[-/G]GGGGGGGGGGTGTTG | 10580 |
rs559882687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467214 | GATGTCTGAGGCATG[A/T]TGTGAAAAAAAATAT | 10580 |
rs559889882 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557715 | TCTCAGTCCACCCCC[C/G]CACCCCCCATCCTAG | 10580 |
rs559904851 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472751 | AGTAAATGAAGAGCC[A/G]GGCACGGTGGCTCAC | 10580 |
rs559919989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403809 | TTGTGATCCACCTGC[C/G]TCAGCCTCCCTAAGT | 10580 |
rs559938499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439961 | TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10580 |
rs559946295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552616 | TTCAAAATTCTAAGG[C/G]AAATGGCTTTCGACT | 10580 |
rs559980410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540491 | ATAAGAGAGGCAGAA[A/G]TGGTGTAAAGATAAC | 10580 |
rs559981931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412984 | ACGGTTCCCAGCTTT[A/G]ATGTGTTTGATGCCT | 10580 |
rs559992665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373197 | GCAACAGGTCAGTAA[C/T]GTCATCTCTGCACAT | 10580 |
rs559997881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538605 | CAGTAACTGGTAACA[A/G]AGGAATTTGGCAAGC | 10580 |
rs560010022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334973 | TTACCTCACTGAATC[C/T]TTATGACTGCCCTAC | 10580 |
rs560040137 | snp | A/C | 4.96151e-05 | 0.00498047 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394971 | AATTTAAAGCTCGGA[A/C]AACAGATATGCTGTC | 10580 |
rs560044062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539818 | CTTCTGATCTTCCCC[C/T]TCCTTCCTATGCTCT | 10580 |
rs560049411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447158 | AAACAAAAACAAACA[A/G]ACAAAAAAAAACAAA | 10580 |
rs560082122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475028 | ATCTTCTGGTCTCCA[A/G]AGGAAGTCCAGCCAG | 10580 |
rs560112520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440743 | ATCCTTGGGCAATTA[C/T]GGCCAATCAGTTTAC | 10580 |
rs560114608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506237 | AGTACAAATGTGAGT[A/G]TGTATGTGCACATGT | 10580 |
rs560118068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525457 | TATAGTGAAAAGTCC[A/C]TATTCCACCCCCAAG | 10580 |
rs560121600 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428886 | GTAGGAAGCAATCCT[C/T]GGCAAGAGCCATCCA | 10580 |
rs560126274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369210 | AACTCTCCTTTCTCT[C/T]CCTCTCCCCTTCTCC | 10580 |
rs560131392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435244 | ATAATTGTAGCCCTC[C/T]GGCCCCAAGCAAATC | 10580 |
rs560132403 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370533 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTCCTTT | 10580 |
rs560177142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328661 | TGGGGAGCACAAATT[C/T]CAGATTTTCTAAATT | 10580 |
rs560193942 | in-del | -/T | 0.465788 | 0.126237 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403565 | AGCCACCCTCATTTG[-/T]TTTTTTTTTTTTTTT | 10580 |
rs560220302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467983 | TCTCACCACAACCTC[C/T]GCCTCCTTGGTTCAA | 10580 |
rs560226326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461316 | TTTGCTCTCAAACTT[G/T]CATTATACATTTGTA | 10580 |
rs560257355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506946 | GCTCACTGCAACCTC[C/T]ACCTCCCGGGTTCAA | 10580 |
rs560260217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434499 | AAGCTGAGGAAGTGA[A/G]ACGGAATGCCTCCTA | 10580 |
rs560294081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528149 | GCCCTTCTCTGCCTT[C/T]TTGGGTGTGTACCTG | 10580 |
rs560304846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558977 | CCCAAAGCCCAAAGA[C/T]TGGTGGCCAGGACCA | 10580 |
rs560340291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392072 | CTGATCTGTCTTGAA[C/T]GCCTTTCTTTGAAAG | 10580 |
rs560346351 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501963 | CTGTTTGTTCTGGGG[A/C]CTTTAGCCACTCAAA | 10580 |
rs560348823 | snp | C/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562412 | CTGACCTCCTCTAGT[C/G]CCCCTCAGAGTTACA | 10580 |
rs560351676 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455282 | TTTCAGCATGATCCT[A/C]ATCATCAATAGCATC | 10580 |
rs560370694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520129 | GTTCGAGACCAGCCT[A/G]ACCAAAATGGAGAAA | 10580 |
rs560374756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343564 | GTGCTGGGATTATAG[C/G]TGTGAGCCACCGCGC | 10580 |
rs560399316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475877 | ATGAGGCTCAGAGAG[A/G]TAAGTCACAAGCCAA | 10580 |
rs560419820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526355 | CAGCCTCTGCACAGG[C/T]CCCACCACAGATCCT | 10580 |
rs560424367 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547016 | GCCAGGATTATAGGC[A/G]TAAGCCACCGCACCC | 10580 |
rs560453330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323450 | TAGGACTGTGTGTGA[C/T]GAAACTGTCACTCTT | 10580 |
rs560465443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454915 | ATGCTGACAAAAGCA[A/C]CAAATAGCCCATAGT | 10580 |
rs560466877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490773 | GCATGGATTATCTCT[C/T]TTAGTCTGCAAAGCA | 10580 |
rs560485351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483678 | ATGGGTGCCCGCCAC[C/T]ATGCCTGGCTAATTT | 10580 |
rs560485781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384729 | CTCTTACCGGGGCCT[C/T]GGGCTGCTATTGGGT | 10580 |
rs560487476 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500238 | AGCCATTTCCAACCA[A/G]GTTACACAAAAAGAT | 10580 |
rs560514355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491706 | AGTCATTGCCCTTGC[A/G]TTATTTTTTTCTTGC | 10580 |
rs560527920 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461475 | AAAATGCGGATTACA[A/C]GTTCTGCAGCCAGAT | 10580 |
rs560555550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352833 | TGGGGAGGGCCTGAC[G/T]GACACCCCATGAGCT | 10580 |
rs560592144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95398852 | TCCAACACCCACTTT[A/G]GGAAAAGCTGTTGTA | 10580 |
rs560607756 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539825 | TCTTCCCCCTCCTTC[C/T]TATGCTCTTTCCACC | 10580 |
rs560610155 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375862 | ACGGACAACCAACAT[A/G]ACTGCTCCCCACTTT | 10580 |
rs560619300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514739 | GAAAAACCAGAAGAC[C/T]CATCATCATTCATAG | 10580 |
rs560624487 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429341 | GATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 10580 |
rs560637498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450550 | CTCTGTTGCCTAGGC[A/G]GAGTGCAGTGGCACG | 10580 |
rs560646889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456950 | ACACTCCCTAAATCA[C/T]ATTTTGCCACTTTTG | 10580 |
rs560665597 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344264 | GCTCCCAAAGAACCA[C/G]TGCTGGTGAGAGGGT | 10580 |
rs560694883 | in-del | -/AGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323013 | TAGAAGCAAGCATCC[-/AGG]AAATGAAATGGGAAA | 10580 |
rs560697395 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450493 | ATAAGTCTGTGTGAC[A/G]TTTGTGATTACAATT | 10580 |
rs560712471 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434501 | GCTGAGGAAGTGAGA[C/T]GGAATGCCTCCTAAA | 10580 |
rs560727081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469834 | AAGGTTCTCAAAAGT[C/T]AGCATACAGCACAGC | 10580 |
rs560728177 | snp | C/T | 0.000367343 | 0.0135476 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337213 | ACTCAGAGGTGACAG[C/T]GTGCATCTCGGGGGA | 10580 |
rs560730475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486017 | ATGAACCTCTGGTGA[G/T]ATAAAGCAATATGGC | 10580 |
rs560749582 | snp | C/G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499999 | ACCCCTTATGCAAGA[C/G/T]CACAACCAGAAAAAT | 10580 |
rs560750804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520662 | GCTTATAAATGCCTA[A/G]ATATACTTCAGCAAA | 10580 |
rs560756254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507747 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 10580 |
rs560762777 | snp | C/T | 6.60066e-05 | 0.00574447 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410583 | CCAAGTATCATGGAA[C/T]AGCTATGTTGATTCC | 10580 |
rs560771234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364035 | GTTGATTAAGATTTA[C/T]AGATCCATCCATTCA | 10580 |
rs560776238 | in-del | -/GGTGGGGGG | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433020 | TACGGAAGTGGGGGC[-/GGTGGGGGG]GGTGGGGGCGGGTGG | 10580 |
rs560793550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468114 | ATTGTTCTGGCTGGT[C/T]GCGAACTCCCAACCT | 10580 |
rs560797317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380517 | CTTCTATGTTTCTTA[C/T]GTACAGTATCTTCTA | 10580 |
rs560816412 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447412 | GGCCTCAGAGGTTGC[A/G]GTGAGCCAAGATTGC | 10580 |
rs560829679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317269 | TCTCCCAACATTATA[C/T]TCATGCCTGAGCAGA | 10580 |
rs560865637 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478202 | CACCTCCACCAACTA[G/T]GAGAATGATCTTACT | 10580 |
rs560895569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508559 | GTACCGTCAAGAATG[C/T]TCCTATCCTCTGAAA | 10580 |
rs560902986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449598 | CCATGCCCAAACTCC[A/G]CTACCAATATCAAAC | 10580 |
rs560904623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500565 | TTTTTATGCAATTAC[A/G]TATGGAAATGATAAT | 10580 |
rs560906797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509413 | ATTCTGACAATCCCC[C/T]GGTTTTATTTGGTCT | 10580 |
rs560907455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386883 | TTGGGAGGCTGGGGC[A/G]GGAAGATTGCTTGAG | 10580 |
rs560921059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373329 | AAGCCTAATGACTTA[C/T]GATCATTTCTTTACT | 10580 |
rs560922458 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559906 | GATGCTGCTGACCCC[G/T]CTGTGTCCACCCCAC | 10580 |
rs560927831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528194 | TTTAAAGATAGCTCT[C/G]AATTTCCCCCACCTG | 10580 |
rs560941932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339569 | AAAGGAGAACATCAG[A/C]TTTGTGTCCCTAAGC | 10580 |
rs560963438 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442945 | TCATGAGTATGACCT[A/C]TCTCTCCCTTTTTCC | 10580 |
rs560997683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408479 | GCCAGAGGCTCAGTG[C/T]CCCTCTGTTTCTAGT | 10580 |
rs561010852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443528 | TCAGAATGGGCATTT[A/T]AACAAAATCCCAGGT | 10580 |
rs561051871 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471376 | GCGCACTGGTAAATC[A/G]TAGGGCATGAGTCAG | 10580 |
rs561058152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372775 | TTTACAGCTGCATTC[C/T]TAAGACAGAAATTTG | 10580 |
rs561063275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535967 | CATTTGCGGGCACCA[C/T]TGAATAGCCACCCTG | 10580 |
rs561063713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541876 | AAGGAGGCCTCCCAT[A/G]ACCCCCGCAGTGCTC | 10580 |
rs561073109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430394 | GAGGCCGAGGCTGCA[A/G]CAAACCATGATTACA | 10580 |
rs561084368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331489 | TCTGGTCCCAGCCCC[C/T]TCTCCAGAAACCCCC | 10580 |
rs561087695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516618 | ACTCATTAAAAAAGC[A/G]CACAAAAATTAGAGA | 10580 |
rs561097912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465177 | TCTGAATTTTAACAC[A/G]GTGCCTTGGATGAAG | 10580 |
rs561141368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403681 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 10580 |
rs561148721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436370 | TCCAGGGCCCCACAC[C/T]GTGGGTGCAGAGGGG | 10580 |
rs561175110 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536116 | CACGGCCGGCTGAGA[C/T]GGGGAACATCAGGGG | 10580 |
rs561182256 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521911 | TGATCCCCTTGCCTC[A/G]GCCTCCCGAAGTGCT | 10580 |
rs561191014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471394 | GGGCATGAGTCAGGA[A/G]GAGAGTGGAGAGGAG | 10580 |
rs561195081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394322 | GTACAAAGCCTTGGG[C/T]AGTTGGGTAAAGGCA | 10580 |
rs561207189 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510299 | GGGCTCATCTAAAGA[C/T]AATAAGGTTTTTGTC | 10580 |
rs561211669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429947 | ATGCTTATTTGGATT[C/T]GATGATCTCAATTTA | 10580 |
rs561227083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345674 | AATCCATTATTAGAT[A/T]AAAAGCCAGCTGTTT | 10580 |
rs561244439 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325722 | ATGTCCAGCTTTTTT[G/T]TTTTGTACTTTTAGT | 10580 |
rs561255786 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416345 | GGTTAGACTCCTCCT[A/G]GTATCCACAATTCTA | 10580 |
rs561264373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402437 | GGGCATTTCCTCTTA[A/G]TCTTTTTTTTTTTTT | 10580 |
rs561303073 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464992 | CCTGGACAGGAATGA[A/G]ACAAGGGCTCTACCT | 10580 |
rs561311303 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446874 | ATCTAATCTTGGGCC[A/G]GGCTCAATGACTCAC | 10580 |
rs561312681 | snp | A/G | 0.000247253 | 0.011116 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95318360 | TTCCATGACATCAAC[A/G]ATATCTCCATCGCGG | 10580 |
rs561352206 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424441 | TTAATTCAACCAACC[A/G]TGGATCAAATATTGG | 10580 |
rs561353428 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432304 | GACTGTCCCAGGGGA[C/T]CGTAAGAGACACACA | 10580 |
rs561378601 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410156 | AAAACGTGTTTTACA[A/T]TCCAGAAAATTGTCT | 10580 |
rs561381130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556412 | TCTCACTCTGTCCCC[C/T]AGGCTGGAGTGCAGT | 10580 |
rs561401239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424759 | TTACTGCAATGTACC[A/G]GCTTGTATGACCAGG | 10580 |
rs561403735 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424167 | TTGCAGGTGATGCTG[A/G]GACTGCCAGTCCGTA | 10580 |
rs561404635 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396119 | CTATCAGCTGACTGG[C/T]GGCACAGGCAGCGAT | 10580 |
rs561407023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325111 | AGGCGGCAAGGGTGC[A/C]GAGGACCTCAACTGC | 10580 |
rs561421687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359684 | ACCATGAATACACCC[C/T]TAAGATAAGCGGCAC | 10580 |
rs561424131 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311348 | CAGATTGCATTTTCG[A/C]CCACCCATACCAAGA | 10580 |
rs561430069 | in-del | -/ACC | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472829 | GGTCAGAAGTTCAAG[-/ACC]ACCAGCCTGGCCAAT | 10580 |
rs561443089 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361056 | TATCCTCAGGTGATC[C/G]ACCCACCTTGACCTC | 10580 |
rs561448142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544068 | AGGAAGGAAGGCTCC[C/T]TTTACATTCCAGGCT | 10580 |
rs561455206 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | SORBS1 | GRCh38.p7 | 10:95397248 | GTGGATCTGTTTAAA[C/T]ATAGTCTTGTACCAG | 10580 |
rs561459473 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453930 | TGAAACACTGTAAAT[G/T]GTTGTGTTATAAAAG | 10580 |
rs561469595 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354685 | GTGCCTGTGGGGAAA[C/T]CAGTCCTACTTTTTG | 10580 |
rs561486267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531066 | GCACTAAACTTCCAA[C/T]TCAGAGGTGCCAACT | 10580 |
rs561489052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444801 | GATACCTCAACTCAT[A/G]CATGATAAGTAATCA | 10580 |
rs561496153 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345823 | GGTATAGATAGAGCA[A/T]GCAGTGTTTCCCAAC | 10580 |
rs561547779 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95333757 | GGTGACAGAGTGAGA[A/C]CCTGTCTCAAAAAAA | 10580 |
rs561561717 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495647 | CACTGTATCCCAATA[C/T]AGTACCTTGGAGCCC | 10580 |
rs561570388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488229 | CTTGCTAATAATTCA[C/T]TCAGCTGACCAGATT | 10580 |
rs561578616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453061 | GAGGCCAAGGCAGGC[A/G]GATTACTTGAGGTCA | 10580 |
rs561583318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393101 | GTTTCTTCACCAATG[C/T]TTTTGTGTGGTAATC | 10580 |
rs561599273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326598 | TTTTTTTCAGGGGAC[A/G]GAGACATGGCATGGG | 10580 |
rs561604538 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524501 | AGAGCACTTATTAAA[C/T]TTGATTGAGTTACTT | 10580 |
rs561610404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438487 | CACCTGGTGCCTGGG[A/C]TTCCGCATGCTGGCC | 10580 |
rs561646789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480333 | GAGGAAAAGCTCCCC[A/G]CGTGGTCAGAACATA | 10580 |
rs561660524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341193 | GTACAGACAGCACCC[C/T]CAGACTGGGGTGTGA | 10580 |
rs561661261 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525940 | CTGGAATTTATGTCC[C/T]GGATGGAAGAACTAA | 10580 |
rs561662108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550942 | CAGGAGCCACTAAAC[A/G]AGTGCCCAACTCATG | 10580 |
rs561686141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327249 | AAACAACCAGCCCAG[C/T]GCATGCATACACACA | 10580 |
rs561702683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460081 | GAATGAGACACAGGG[A/G]TGAGGAGTCCCCAAA | 10580 |
rs561704231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446610 | ACTATGGTGTTTTGC[C/T]TCCATAGCTCCCCCA | 10580 |
rs561704685 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408220 | AAAATGTAGAATCTC[A/G]TCTCCTCCACCCCAA | 10580 |
rs561712485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348824 | TCACCCAAGTCCTAC[C/T]GAATGGGATTGAAGT | 10580 |
rs561714967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374820 | AGGTGGCGCTGTTCA[C/T]CCAGGACAGCTCAGC | 10580 |
rs561721517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473689 | TATAATATATATATA[C/T]ACACACACATACATA | 10580 |
rs561725784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411753 | GCCCAATGCCCTGCA[A/G]ATAGCAGGTGCTAGT | 10580 |
rs561725818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466357 | GGGGCAGGAGAATCA[C/G]TTGAACCCGGGAGGT | 10580 |
rs561758285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348026 | GTGAGCCACTGTGCC[C/T]AGCCTTCCACAGGCA | 10580 |
rs561770734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360964 | GACTACAGGCATGCG[C/T]CACCACACCCGGCTA | 10580 |
rs561776131 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529328 | GTTCATAAGCATACA[C/T]TGTCAAGATTCTGGA | 10580 |
rs561781628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388073 | CAACATTTGCCTCCC[A/G]GGTTCAAGCAGTTCT | 10580 |
rs561781675 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424634 | TATATAAGGGACTTG[A/G]GCATCCTCAGATTTT | 10580 |
rs561800661 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316476 | AAAGAAGCAAGTGAA[A/G]AGTTCAGGGATGCAA | 10580 |
rs561808084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517245 | CTGAAACCTATGCAA[C/T]TGAAAAGAAATAAAA | 10580 |
rs561814364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340530 | ATATTGTAAAACCCA[G/T]TCCCCAACACAATGC | 10580 |
rs561840175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375656 | AGGAAGTGAAAACAA[C/T]GGCTGAAATAATGCC | 10580 |
rs561843722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453554 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGACC | 10580 |
rs561868337 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418850 | GCAGAAGGACCACTT[G/T]AGTCTGAGACCAGCC | 10580 |
rs561883753 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544423 | GGAGCCCAGGGACTC[C/T]GAGAAGACACTCCTG | 10580 |
rs561889624 | snp | A/C/G | 0.000264587 | 0.011499 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341427 | TGAGAAAGGGAAAGA[A/C/G]GTAAAAGAGAACAAG | 10580 |
rs561910089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376620 | CATCTTTAATGGCAC[A/G]TGAGTAGGTAGGAAA | 10580 |
rs561927781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545547 | AAGTAGCCGGGAGTG[C/T]TGGCAGGCGCCTGTA | 10580 |
rs561928504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474554 | ACTGAAATTTGGAGG[A/G]CAGAATGTCCTGTTG | 10580 |
rs561962639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504411 | TTTACCACCCTGACA[A/G]GCAGGTTGGTCACCA | 10580 |
rs561972342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375438 | AAATATCCTACATCA[C/T]AGAAATCATTCCCTA | 10580 |
rs561977126 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547092 | TGTATTTCTATGCCA[C/T]GCTGAGAATCAGGCT | 10580 |
rs561979785 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493407 | CTGTCTATCTCCACC[C/G]CAGGACCTGGATTTC | 10580 |
rs561984856 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378276 | TTCTCCCAGCTCAAA[A/G]AAAATCCTTGGAAAA | 10580 |
rs561992179 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429767 | GACTTACCCACAGCC[C/T]GAAAGGAAGATGGCT | 10580 |
rs562018220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355393 | CATTTCTCAGTTGAG[A/C]TAAACGGCCAATTTT | 10580 |
rs562027896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366891 | CAGGCTGGTCTCAAA[C/T]TCCTTACCTCAGGTG | 10580 |
rs562041610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397456 | AAAAACCAAGAGTCC[A/C]AAACCTCAATCTACA | 10580 |
rs562049811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489765 | TGTGTCCCCTTGGAC[A/G]GGGGAGTCTAGACAG | 10580 |
rs562070520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343440 | TACAGACATGCGCCA[C/T]CAGGCCCGGCTAATT | 10580 |
rs562078589 | snp | G/T | 0.000137922 | 0.00830312 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355863 | TGATGGGGCTGACTG[G/T]GGAGGTCTGGCTTCT | 10580 |
rs562081681 | snp | A/C/G/T | 0.00164041 | 0.0285952 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384388 | CGAGCATCCAGCCCC[A/C/G/T]CTAGGGATCCCAGCG | 10580 |
rs562090800 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555480 | AATGAGGGCCCACAA[C/T]AAACACATTTTCGTA | 10580 |
rs562117910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404707 | ACCCACAGAGCGCCG[C/T]CTGGTAACAGGAATG | 10580 |
rs562147724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496541 | TCCACCTACTCCACT[A/G]ATTCAGTAGGAGGGA | 10580 |
rs562159895 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545809 | GTCCCATTTTCCTCC[C/T]TGTCAATTTGTTATA | 10580 |
rs562179213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396778 | GTCCTGGGATTACAG[A/G]CTTGAGCCACCGCGC | 10580 |
rs562183006 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405286 | TCTACAAAAAAACTT[A/T]AAAAAAAAAACTAGC | 10580 |
rs562218675 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522497 | CACTAGTGCCCACCA[A/G]CTTCATGTCAATATT | 10580 |
rs562232726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432773 | AGAGGTTTACTGTGC[A/C]TCATGAAGTTAGGGG | 10580 |
rs562243407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507114 | GATCTGCCCACCTCA[A/G]CCTCCCAAAGAACTG | 10580 |
rs562270013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335851 | TCAGGTCTCAAAACA[C/T]CCTAAGGCTACCTTT | 10580 |
rs562270635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525125 | AACAAAGCCGATTGT[A/G]CAAAAGTACGGGCTG | 10580 |
rs562316232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499679 | TCTTATGTTTCCAGA[A/T]AAAAGGAAGACCACA | 10580 |
rs562352628 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490583 | GCAGCTACACTGTAA[C/T]ACTTATATCTGGAAT | 10580 |
rs562387384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440560 | GATGAGCAGGGATCT[G/T]TTCCCATCTCTGTCT | 10580 |
rs562398347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547248 | ACATCCATTATGTAC[C/T]TCTAGAGCACCCTCA | 10580 |
rs562408767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525633 | TACAGAGTCCCATGT[A/C]AGTACTTAAAAAGCT | 10580 |
rs562413400 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373514 | TTGGGTGGCTAAAGC[A/G]AAGGGGTGGAGGAAG | 10580 |
rs562415580 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519088 | GTCTCTTCTACAAAG[A/C]CTTACAAGGTCAAAA | 10580 |
rs562416933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427151 | GCAGTAAGGACTGGA[G/T]CCAACTGGTACAGAA | 10580 |
rs562433627 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396866 | CCACAAGGCAGTCAT[A/G]GGCTGACACAGGGAG | 10580 |
rs562445188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323197 | ACCCAAAGCCAGTTT[C/T]GGTTATTTTGTTGAC | 10580 |
rs562450810 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461389 | ATAATCTTTGCAAAC[G/T]TTCCCACTGTATGTA | 10580 |
rs562454427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433496 | TGCAGCTGAGCTATG[C/G]AGAACGCCACAGTTT | 10580 |
rs562474267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533980 | GCTGTCTAGAAATCA[C/T]TGTTTTTGAAATGTC | 10580 |
rs562478191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413129 | AGGGATGTCAGTAAA[C/T]GCTTAGTTCCATCAG | 10580 |
rs562497598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468741 | CAATGTTTTCAGCCT[C/T]ATTACATAGAGAAGG | 10580 |
rs562498477 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423737 | TCACTGTTACGCCCA[G/T]TTAGTTTTAGTTCAG | 10580 |
rs562500099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455426 | CGGTCAGTGCTCCTT[C/T]GAAGAGCTTACAGCA | 10580 |
rs562502599 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441287 | ACCCTTGATAAAACA[C/G]AGCTGAACCAGGAGT | 10580 |
rs562506446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559162 | AGTTAGGATGACCTG[A/G]TCATTATCAATGCTG | 10580 |
rs562525331 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519732 | GGGGAGAAGGAAAAA[C/T]ACAGAAAGGGGAACA | 10580 |
rs562534311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540562 | AGGCATACTAGGTAT[C/T]CAAAAACATATGCCT | 10580 |
rs562537168 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349168 | CACCCACGGTGCATT[G/T]CTGTTTGCATGTATC | 10580 |
rs562552067 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314609 | CCAGCAGCGTTACAG[A/G]ATCAGCTGGCTCCAG | 10580 |
rs562552290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422302 | AAGCATGAAACTGCA[G/T]AGAAGGTTGAAAATC | 10580 |
rs562554304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429870 | TCTCTTTTCCTCCTT[C/T]CTCATCACAATTCCA | 10580 |
rs562559853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328731 | ATTCTCTATTTTCTT[A/C]TCTTCCCATCCTCCC | 10580 |
rs562565363 | snp | A/C/G | 0.000892023 | 0.0211004 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434607 | TAGAGAAAATCGACC[A/C/G]ACCCAAGGAGATACC | 10580 |
rs562584111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384813 | CTGTTTTATATGGTA[A/C]GCTTTCATACACATC | 10580 |
rs562585593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553161 | AAGGCTGCAATGAGC[C/T]ACAATCGCACCTCTG | 10580 |
rs562611836 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322631 | TAGCCACAGAATTCT[C/T]ATAAATAATATTTCT | 10580 |
rs562645974 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555621 | GCAAGGCCCACTTTA[C/G]ATACTAAAGTACTTG | 10580 |
rs562652772 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474502 | TATTATTTTGAAAAG[A/T]GAGGGTGCCAAGTTT | 10580 |
rs562673323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344321 | TTTTTTGGAGCATCA[C/T]GGTGTACATCAGCAC | 10580 |
rs562694762 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403969 | CCACCCTTGTTTCCC[A/G]TATGAGGAAACTGGC | 10580 |
rs562723097 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442010 | CTATAACCACCACCG[C/T]AATCACAATATACAG | 10580 |
rs562732805 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541622 | GCCATGGCTCCTCTA[A/T]CCCACTGGATCAATC | 10580 |
rs562732840 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500857 | GTTTCCTCCCCTGTA[A/C]ACAGGCATAACATCC | 10580 |
rs562769871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379631 | AGACGTAAGTACCTC[A/C]AATGGAAAAAGCATT | 10580 |
rs562771256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449774 | AGCAAATTCAGCCCC[C/G]CAAACAGTTTCAAGT | 10580 |
rs562783702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450905 | GAATTATGGGTAACT[C/T]CTTTTTTCTATTTTC | 10580 |
rs562786833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495767 | TGCTTTCCGAGCTCA[C/T]GACATACTCTCTTCT | 10580 |
rs562798248 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324024 | GGCCTTCTAGATGGG[C/G/T]GCTTAGAAATCTTTT | 10580 |
rs562824793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514833 | GGCCTTGAGGCAGAA[A/G]TAGAGTGTATATGAG | 10580 |
rs562830131 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399659 | GGAAGTCACTTAACT[C/T]TTCCATGCCTCAGTT | 10580 |
rs562830137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540984 | CAGCCCCTTCTTCCC[C/T]ACAACTCCTCATCCA | 10580 |
rs562851748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476546 | GGTTCTAGCACAGTG[A/C]CTTGCAAATAAAAGG | 10580 |
rs562863428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560613 | GCTTGCTGTCCATGT[C/T]GGTGATGAGCTGCCT | 10580 |
rs562877092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548416 | TTACTGAATTATTAC[G/T]ACTTATGTGTCATGC | 10580 |
rs562887251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520751 | AAAATAAAGGAAGCG[C/T]TATGCATTCATACTC | 10580 |
rs562887803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316559 | CATTAGAGAACTGGT[A/G]CTCCTTCCCACACCT | 10580 |
rs562916314 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522947 | CCCTCCTCAGTTCTG[A/G]GTGCCCTCTCTTCTG | 10580 |
rs562953131 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549015 | GAGACCTGTTCCTAG[A/C]TCAGTCTTAAACAAA | 10580 |
rs562970648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457461 | CTCCCTGTTGTGAGG[A/T]TTAATCGAGATAACC | 10580 |
rs563000630 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447095 | GCAGTGAGCTGAGCT[C/T]GCACCACTGCACTCC | 10580 |
rs563010273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541967 | GGCTGTGAGTTGTCA[C/G]TACACTGTCTGAGCT | 10580 |
rs563035043 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443088 | GAAAAACAAGTCCTC[A/G]GGATATGTAGAACCT | 10580 |
rs563036376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509233 | AGGTACCTTCTAGGA[C/T]CGCCCCCTTGCCCCA | 10580 |
rs563036878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450429 | AACTAACATAGACCA[C/T]ACAACATGGGAAAAG | 10580 |
rs563062982 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426471 | TGGGGGCTTTGAGCC[A/G]CCAGGAGCTCAATCG | 10580 |
rs563066251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457051 | GGTGTCGAAAAATCC[C/T]TTAGAACTCAAAGAC | 10580 |
rs563087732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408724 | GCAAAGCAGAGCTGC[C/T]AGGTTAGGCAAATTC | 10580 |
rs563107556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372855 | ATTCAGAGGTTACAG[A/G]TGACTTCTAACTCTG | 10580 |
rs563110230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358689 | ACACACACACAGACA[C/T]GCACATGCACAGACA | 10580 |
rs563118557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515383 | GTAGGGTGGAGGCAG[C/T]TACTCTGCTCCCTTG | 10580 |
rs563127355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471478 | ATCCCAGCACTTTGG[A/G]AGGCCCAGGTGGGAG | 10580 |
rs563163003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364071 | CAAACATTTACTGTA[C/T]GCTTTCCTTTGTGTC | 10580 |
rs563165030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371745 | CAGAGTGTGGTGACA[A/G]TGACAAATACTATAT | 10580 |
rs563230947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415686 | GGTGGTTTTCCTGTG[C/T]CGGCTGTGCGGGAGA | 10580 |
rs563243580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494465 | TCCACTTTGTGGTCA[C/T]GTAACGACCTGAGCA | 10580 |
rs563263130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472086 | AGGGTGAGGACACTT[C/T]GCAGTCTTTTCCAAA | 10580 |
rs563276648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353406 | AAATAATAACTATAC[A/T]TCAAATGCTTCCTCT | 10580 |
rs563276929 | in-del | -/TC | 0.0279526 | 0.114869 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506057 | ATTTATTGCTGCCAA[-/TC]TCTCTCTCTCTCTCT | 10580 |
rs563301280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502726 | GGAGCACCAAAAGGA[A/G]GGAATTAAATTATTA | 10580 |
rs563304962 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449425 | TTTAGTAAAGATGGG[G/T]TTTCACCATGTTGGC | 10580 |
rs563318554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437170 | GCTGAGCAAGGGATA[G/T]TTCAGGCTGATAAAT | 10580 |
rs563332502 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330908 | TTGGGCATTTTGTAC[A/G]CACATTTTTCATCCA | 10580 |
rs563336223 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339382 | GCCTCTGCATGCCTG[C/G]GGCCTCTGCCTGCAT | 10580 |
rs563341474 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529024 | CCCTGGAGGACCCTA[A/C]AAAGACGGTCAGTTT | 10580 |
rs563381231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487094 | TTAAGTTCCACTCTG[C/T]GAGAAAAGACAACAA | 10580 |
rs563396424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352892 | GGGAATGGAGTGATG[C/T]TTGAAACTGCCACAG | 10580 |
rs563399700 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444453 | TTCCACTGTGAAGCT[A/T]TCTTAACTGAAACTA | 10580 |
rs563399740 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410537 | ACAATGGGATTTGTG[A/T]AAATTTCTGTGAAAT | 10580 |
rs563404472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486141 | TCTGGACACCGAATT[A/G]GAATTCAGTTGCCAC | 10580 |
rs563421165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437630 | CCTGTGTGGCAGGAG[A/G]TGCTGGGGTCACAAT | 10580 |
rs563427051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536022 | AAATCACTGCTCGTC[A/G]CACAGCCCTTTGGCA | 10580 |
rs563436693 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503326 | GCTCTTTATATCCAA[G/T]TTAAACCTCTGCTGC | 10580 |
rs563479786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522769 | CCAATTTTATCATCC[C/T]AATTTATTGGAGAAG | 10580 |
rs563484174 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344735 | TTTGAGTAATTGACT[A/G]TGGCGAAATGTAAAA | 10580 |
rs563485728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424859 | TCACAGGGAGTATGA[C/T]TCTTTGATTCTCTCC | 10580 |
rs563493657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510891 | AAGATCCTTACTACA[A/G]ACTGGTTCCACCTCA | 10580 |
rs563508003 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356149 | CTCCATGAACACTGC[C/T]GCCACTGCCTTCTCT | 10580 |
rs563522507 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384996 | ACTCGGAGTGAGTAT[A/C]TAAACTGCATCTCTG | 10580 |
rs563531462 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512640 | TCCCCTGAAATCAGC[C/T]CACCTGCTACTGTAT | 10580 |
rs563533085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557177 | GCTGTAGCTCCAGAC[A/C]TTGAACTATTATCAC | 10580 |
rs563536618 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95420615 | GGCTCATTCGCAGCT[A/C]CTGGTTCTAACCAGT | 10580 |
rs563555438 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333053 | AGCAAAAAGAGGTAG[C/T]TCTGCAAAGCTGTCT | 10580 |
rs563561704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451873 | AAAAATGTTAAAAAG[C/G]TGAAAAGCAGTCTGT | 10580 |
rs563577001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390217 | GTAGAAGAGGCATCA[C/G]AAAGCATGGGAAAAA | 10580 |
rs563581863 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516686 | CATTTCTCTTCCCCA[A/C/T]GCTCCACAGGTATAC | 10580 |
rs563584100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430537 | GGGCATTGTGTTCTA[C/T]GTCAATGCCACACTG | 10580 |
rs563600228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380574 | AGTAGTGGGGAGAAG[A/G]CGAAATTCTGTGCTC | 10580 |
rs563610287 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485152 | CTTCCCCAGTCTTTC[-/A]CCTAGATCTAATCAG | 10580 |
rs563623505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424365 | TTCACTGCCATTTGT[C/T]TTCTCCAACCCGCAA | 10580 |
rs563628670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332245 | GGCTCTGACACCCTG[C/T]CTGGCATTTTTTTTT | 10580 |
rs563654066 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311451 | AAAGCAAATCTAGAC[A/C]CATTATACATATTTT | 10580 |
rs563668079 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95385164 | CTGTATCTTCTGAAC[G/T]AAAAATCAGACCACA | 10580 |
rs563674580 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509619 | CAGGATTTTTCTTCC[-/T]CAAAAAAAAAGAAGA | 10580 |
rs563695140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517845 | CCATATCACTCAGCC[A/G]AAAAGGCTGATTATT | 10580 |
rs563722483 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510139 | AATAACTCACCCTTC[C/T]CCCCACCAAAAAAAG | 10580 |
rs563738832 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514348 | ACCAGCTCCCTTCCT[A/G]ATGCTGGTTTATTTC | 10580 |
rs563740016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419069 | TGTCAAAAAAAAAAA[A/C]AAAGTTTTTTGAGTC | 10580 |
rs563748235 | in-del | -/TG/TGTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378735 | CCGTCCTACTACATA[-/TG/TGTG]TATGTGTGTGTGTGT | 10580 |
rs563777494 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491892 | ACTCCCACTTTACAT[A/G]AATTAAATGTAAGCA | 10580 |
rs563810485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531209 | GCCCTAAAAGGCTAA[A/G]CGACTTGCCGGAGGT | 10580 |
rs563813789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319434 | CTGGAGACAGCTGGA[C/G]TGCTTGTGGTGAAAT | 10580 |
rs563826796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445985 | TTGGAATGCCTCTTA[C/T]AAGTCCCCTCCAAAT | 10580 |
rs563880349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544761 | TGGAGCTCCTTTGAC[C/T]CCAGGAAGGGAAAAT | 10580 |
rs563886623 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439230 | TTCATGTAGGTGATA[A/T]TTTTGTTTCCTTGGA | 10580 |
rs563903610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423990 | AAAAGAGCTGGAGCA[A/G]AAGGCAAGGTAGGGT | 10580 |
rs563916410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537378 | ACATGCTGGAGAAGC[C/T]ACCCTGTTATGGTTT | 10580 |
rs563922550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431920 | CCTGCTCCCGCAGCT[A/G]GCTAGTGGCCAATCC | 10580 |
rs563929444 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354212 | CTTCCTCTTCCCAAA[G/T]CCCCAAGAAAAGGGG | 10580 |
rs563930842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348693 | CTTTCACAGTATTGT[A/G]TTACTTACTACAGGA | 10580 |
rs563933263 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533843 | AACTTTATTAAAAGG[-/T]TCATTTTCCTGGCCT | 10580 |
rs563937649 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95311870 | CCACTGCAATGAAGA[A/C]AAATAAATGAACAGA | 10580 |
rs563938697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551847 | TGCAAATATGTTCCA[C/T]GTAAACACATGAAAG | 10580 |
rs563944038 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455919 | CCAGCATGGGTAGCA[A/G]AATGAGACCCTGTCT | 10580 |
rs563949367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381888 | ATGGCTGTAGTGTAA[A/T]CAAAGAACTGTTATA | 10580 |
rs563969780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446663 | ATCTGGAAAGGAAAA[C/T]TGCATCATCCTCAGC | 10580 |
rs564001633 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457241 | ATAGAACACACCATG[C/T]TGGAAGAAAAGAACT | 10580 |
rs564001926 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386365 | TACTGGTTGAGCGTG[G/T]TGGCACATGCCTGTA | 10580 |
rs564003199 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432340 | ACACACACACCCCCC[C/G/T]CCCCCAAGAGGTATC | 10580 |
rs564008733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546462 | GGAGGAGCAGGCATG[A/G]AGCAGGCATGTCACA | 10580 |
rs564008830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348125 | CCAAGTGAATGATCA[C/T]CTTATAATCTAGTTA | 10580 |
rs564046677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355137 | CACCCCCCACCCCAT[C/T]TTTTGGATTTATTTG | 10580 |
rs564054834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530579 | TTAGTATTTCCTCTG[C/T]TCAAATCTGAAAAGT | 10580 |
rs564064774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426603 | CATTTCCTGGTTGAA[A/G]ATGCTCTGAGAACAC | 10580 |
rs564076023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552398 | CAGAGTGAGACTCCA[A/T]CTCAAAAAAAAAAAA | 10580 |
rs564077738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383235 | GCCTAGCCAACACGG[C/T]GAAACCCTGTCTCTA | 10580 |
rs564077821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412355 | TATTCTTCCTTCTTT[C/T]TCTCAACTAGCTACA | 10580 |
rs564102698 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385638 | CCCATTTTTATTTGT[C/T]TCAGGTCTCCCTTGG | 10580 |
rs564116310 | in-del | -/AAAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547725 | AAATGCCATCTCAAA[-/AAAT]AAATAAATAAAGTAT | 10580 |
rs564119860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426964 | TCAAAAAGACTCTAA[C/T]TTAATGGAGGTACGG | 10580 |
rs564124760 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353434 | TCTTGTTTCTTTCCA[C/T]GGACAGGTGCAAGTT | 10580 |
rs564129658 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467108 | GGTGATTTGGGGTTA[A/T]CGGTTGTATAAGTTA | 10580 |
rs564134396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376444 | TTAGTTATGAGCAAA[C/T]GACCTGGTGAGCACA | 10580 |
rs564148645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460161 | AACATTGTTTCAGCA[A/G]GGGAAAAAGAAACAC | 10580 |
rs564163945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343514 | TGGTCTCAAACTCCC[A/G]ACCTGAGGTGATCCG | 10580 |
rs564190496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474342 | GTCCTACAAAGCATG[C/T]GAGGCATCTTGCCTT | 10580 |
rs564198092 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552243 | CCCATCTCTACTAAC[A/G]ATGCAAAAATTAGCT | 10580 |
rs564201198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511629 | GGACTGAGTTGGAAA[C/G]TCTCAGAAATGAGAA | 10580 |
rs564216509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334657 | CGGAGATCCGGCACC[A/G]TGCGCACTTCCTATA | 10580 |
rs564228083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557948 | TCCTCCTCATGTTTC[A/G]CTATTCCATCTTAGA | 10580 |
rs564233981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440092 | TAAATAAAAGCATTG[C/T]CTCACTTAATCCTCA | 10580 |
rs564241848 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488982 | AAGATCACATGGACT[A/G]TGGAATCCAATCACT | 10580 |
rs564260232 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535645 | GGATAATATATAATT[A/C]ATCACCTAAACTGGG | 10580 |
rs564279240 | in-del | -/G | 0.0715223 | 0.175059 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509630 | TTCCTCAAAAAAAAA[-/G]AAGAAAAAAAAAAAA | 10580 |
rs564280967 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416218 | AGATATGTTATCAAA[C/G]AGGGAAAAAAGAAAG | 10580 |
rs564334600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454879 | CAAGCTTCACAACTT[A/G]CCTGGGAAACACCCA | 10580 |
rs564335745 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504911 | CTGTCCAGATGAAAG[A/G]GATGGGAGGCTTTCT | 10580 |
rs564359158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327937 | TACATAAGAGGATTG[A/G]ACATAATTTACATAA | 10580 |
rs564362114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368204 | GCATGTACAAAAGCA[C/T]ACTTTAAAATACCAC | 10580 |
rs564364085 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361098 | GGATTACAGAAGTGA[A/C]TCACCATGCCCAGCC | 10580 |
rs564369423 | snp | C/T | 0.00026617 | 0.0115332 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355696 | GGTCTGAGTATGGCA[C/T]GGAGTTTCCATTATT | 10580 |
rs564369690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497386 | ACCACCATATACCCC[C/T]GACTCCACCCCAATT | 10580 |
rs564372032 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480259 | AAACTAGGACAAACC[A/G]GAAAGGGAAGGGGAA | 10580 |
rs564375610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538963 | TGGACCCCAACCACC[C/T]CTCACCTGCTGCAAC | 10580 |
rs564376858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397554 | CATTTTTAAATTTTT[A/T]AAATTTCACTTTTAG | 10580 |
rs564398494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344159 | CTTGTGTGTGAGAGA[C/T]GAACTGAGGGGTCTG | 10580 |
rs564398576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469687 | CCTGCATCATAAATG[G/T]TCATAAAATACCCCT | 10580 |
rs564400446 | snp | C/T | 0.000198801 | 0.00996799 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336610 | CACTTCCTGGAAAAG[C/T]GCTACCCAGGGGCTT | 10580 |
rs564402182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505891 | CCTTGTTATCCCATC[A/G]GCAGACTGAGAATGA | 10580 |
rs564433204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482642 | GCAGCCATGAGAAAT[A/G]AACGATGACATTAGG | 10580 |
rs564446629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321511 | TCAGAATCTAATTTG[A/T]CTTTCAGTGTTTGGT | 10580 |
rs564446940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490685 | TCTCAGAGCCAAACA[A/G]TATTACCTTCTATTT | 10580 |
rs564466436 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383845 | TTTTACAGAGGAGGA[C/T]ATTGAGGCTAAGAAA | 10580 |
rs564485148 | in-del | -/T | 0.251859 | 0.249993 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312364 | TTCTTAAGCACATTA[-/T]TTTTTTTTTTCTTTT | 10580 |
rs564495400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357331 | CTAAAGCTCAGCTAA[C/T]TTCTAAGAAAAGGTA | 10580 |
rs564495479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363833 | GGACTTAAAACAACA[A/C]CATCACTTCTCCAGT | 10580 |
rs564507804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489945 | ATCCACATCATAGGA[A/G]CTGACCAGGTAGTGT | 10580 |
rs564553013 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557962 | CGCTATTCCATCTTA[G/T]AATCATTTCTCTCAG | 10580 |
rs564555767 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525796 | TGCAGGTATATCTGT[A/T]GGACAGATTCCACAA | 10580 |
rs564573393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475220 | GGGGGTGGTGGTGCA[A/G]AAGAGGGAGATACCC | 10580 |
rs564581848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553294 | TTGAGAATTAGCAAT[A/C]AGTACATAGAAACTA | 10580 |
rs564586519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95391258 | TTGATAAAATGAAGA[A/G]TTACTTCATGGGGCT | 10580 |
rs564586837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533782 | CAGCACAGCAAACAG[A/G]CTCACGGCCACATGA | 10580 |
rs564629035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363138 | AATAGGTGCTCACTC[C/T]TCCCTCCTGGGCCCC | 10580 |
rs564641127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462944 | TTAGAAAGGAGGCAA[A/T]GATCCAGTGTCTTCT | 10580 |
rs564644292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559846 | CCATCTGCCTCATCG[A/G]TGTCTGAAGGCTGTA | 10580 |
rs564686038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329542 | GAGAGAATACCTGCT[C/G]CTTATTTTTGTAAGT | 10580 |
rs564687113 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519320 | TCACCACCTCCTGCT[G/T]GTCCCCTCCAGCACA | 10580 |
rs564688032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475841 | AAATTTATGTTTATC[C/T]CAATTTCACAAATGA | 10580 |
rs564689277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526204 | CCACAGAGCCAGGAA[A/G]GGGCAGAGCTCAGAC | 10580 |
rs564689485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448075 | CCAGGCTTCACTGAT[C/T]TTTCCACTGCATTTA | 10580 |
rs564710965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493424 | AGGACCTGGATTTCC[A/G]CAGCAAGAAGCTACT | 10580 |
rs564759103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560433 | TACGACAGCGGATGC[A/G]TGGGGATGCAGAATT | 10580 |
rs564771005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384689 | TACGGTTAAGCTCAC[C/T]GAGTTCAACAGTGTC | 10580 |
rs564776032 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491229 | AATTTAGGCATAAAC[A/C]CCTATCTCTTGTAGC | 10580 |
rs564778863 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536343 | GAACAATGCCGGGGT[C/T]TAGGAAAGTGAATAC | 10580 |
rs564782090 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463267 | CTCAAGGAGGCAGTG[A/G]TCTTATAATCCAACG | 10580 |
rs564809902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420812 | GCTTCATTTCAGCAG[C/T]AAGTGCATTTTTACA | 10580 |
rs564822176 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370703 | CTCTCTCTCGTATAC[C/G]CTTTAATAAACCACA | 10580 |
rs564859725 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393627 | ACACGCTCTCACAAC[C/T]GCCCCCACACTGGAC | 10580 |
rs564869289 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491983 | CCTAATCCAGGACTC[A/G]TACACTATGCTGGAC | 10580 |
rs564869292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316221 | ACTTTGGGAGGCTGA[A/G]GCAGGCAGATCACTT | 10580 |
rs564873128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547281 | ACCTGCACCTCCACA[C/T]GCACTGTATCATACT | 10580 |
rs564890453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522458 | GTCACTGAACATTAT[G/T]TTGGGTTGCTGGACC | 10580 |
rs564902790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380466 | AAACCCAAGGAGCAC[A/G]ACTTTCTTTGCAGGA | 10580 |
rs564904062 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510666 | TAGGTATGTCAGGTT[C/G]TCAAAAGTTTTTGGA | 10580 |
rs564921392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448923 | GACCCTGCAGGATCA[C/T]GTCCCAGTTATTTTT | 10580 |
rs564937943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414360 | AGTGACAGGGGACAC[A/G]GCTCCAGTCATCACA | 10580 |
rs564943028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534757 | GAGCTGAAGAAAGCA[C/T]GAAGCATCTCAGTCT | 10580 |
rs564963457 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389403 | TAGTTAAAGGCCATC[A/T]AGTTCTTTTTTTTTT | 10580 |
rs564966338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500526 | CTCAGAATTTTAAAA[A/G]AGAATGTAAAATATC | 10580 |
rs564979799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315307 | GCCAAATAATGCTGG[A/G]CGGTAAGCAATGTAG | 10580 |
rs564981332 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547776 | ACATATAAGCAGAGA[-/TT]TTTACCTACCCAATG | 10580 |
rs565000402 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392183 | CACGGACAGGGCTGA[C/T]GAGGCCCTGCTGGAG | 10580 |
rs565025609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449485 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10580 |
rs565030310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516065 | TTGACATCCACACCC[A/T]CCCCCCACCAAGGTC | 10580 |
rs565040288 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331655 | TCTGTGAGAAAACCT[C/G]TTATTCTTTAAGGCT | 10580 |
rs565044577 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467450 | GGGCCCCAGCCCTCT[-/G]TCTGCCCTTCAAGGT | 10580 |
rs565047359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476622 | TTTTCAAAGTACACT[C/T]ATTTCCACTTCATAA | 10580 |
rs565081724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541782 | TACCCATGTCATTCC[A/C]TTCCTTTGGAGGGTC | 10580 |
rs565081902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527319 | TAATACCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10580 |
rs565095614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338141 | TTTGTCCAGGCTCTT[C/T]CACAGGGATGTCACC | 10580 |
rs565136322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410049 | CTAAGCAGAGCTGCC[G/T]AGAGCCACATAGTAC | 10580 |
rs565136616 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473284 | GAATGAGGTATCTCA[A/G]TGTGTGATGTGGAAT | 10580 |
rs565137489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424107 | CTGGCACTTCTGATG[C/T]AGTAAGTATGAGGTG | 10580 |
rs565155890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528841 | GGAGAATCGCTTGAA[C/T]CCGGGAGGTGGAGGT | 10580 |
rs565163587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372701 | AGAGTTTAAACCCAG[A/G]ATTTAAAGAGGGGAC | 10580 |
rs565170640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528108 | AACACTATGCAAGAC[C/G]CTTGGAGAATACAGA | 10580 |
rs565203129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416290 | GCATAACATGATTCA[A/C]GCAAAAACAATTCTT | 10580 |
rs565206410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455314 | GGGGCGGGGGTCAGA[A/T]CCACTTTCTCCTCAC | 10580 |
rs565211594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543335 | ACCTGGGAGGCGAAG[G/T]TTGCAGTGAGCTAAG | 10580 |
rs565218404 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345132 | TGGTTTAAAAAAAAA[A/G]GGGGGGGAAGAGGAT | 10580 |
rs565250668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371944 | CTAACCAAGGCTAGA[G/T]AGCACACACAGTCCA | 10580 |
rs565253426 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446340 | CCTATAATTCTAAGA[A/T]AAGTTTTGATGACAC | 10580 |
rs565254586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464223 | ACTTGGGAAACTGAG[A/G]AATGGGAATCACTCG | 10580 |
rs565256927 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559905 | TGATGCTGCTGACCC[-/CT]CTGTGTCCACCCCAC | 10580 |
rs565259408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471343 | CTGTAAACTGCCCTC[A/C]CAGTAAAGGCAGAAA | 10580 |
rs565264967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324571 | AGTAAAAGAAGAGGC[A/G]GAACTAAATGAGCCA | 10580 |
rs565266408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332089 | AATCCACCTCAGTGC[A/G]CTCAGTCCTCTCTCA | 10580 |
rs565266507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470848 | GCCTGGCCAACATGG[C/T]GAAACCCTGCCTCTG | 10580 |
rs565302393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509937 | TAGAAGAAAGCAGGG[A/G]AAGGGCTAATATACA | 10580 |
rs565318027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464674 | ATACTCTGCACACTC[G/T]GGCATTCTCTCTGCT | 10580 |
rs565320851 | in-del | -/GAGAAAA | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374595 | AGGTTTTAAGAAAAG[-/GAGAAAA]GAGAAAGGGTTAGGA | 10580 |
rs565328176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477295 | CCTGGAGAACTCAAC[C/T]CTGGCAGAGGCATTG | 10580 |
rs565331240 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556243 | GACCACAGAAGAAGT[C/G/T]GGGGGATAAATCAAT | 10580 |
rs565335216 | snp | A/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417812 | TTTAGTAGAGACGGG[A/G/T]TTTCACCATGCTGGC | 10580 |
rs565340603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338902 | TTGGTAGAGATGGGG[C/T]TTCACCATGTTGCCA | 10580 |
rs565356439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429922 | CACATAGATAATGCT[A/G]AATGAATGTATGCTT | 10580 |
rs565357922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332331 | ATCTTCCAGGATGTA[A/C]TGTTTGTGACTCTCT | 10580 |
rs565358997 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472594 | ACAGGCCTGTCTACA[C/T]GTCCAGCACAGGTCT | 10580 |
rs565360667 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444767 | ATGAATGGAGATGTC[C/T]TGTGAACCAAACAAA | 10580 |
rs565363696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450988 | CTTTTTAGCTCCTAC[A/G]TGACATTTGATATGC | 10580 |
rs565383118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379858 | TTCTGTCCATGTGAT[A/G]AAAACAGCAGGAAAC | 10580 |
rs565384825 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464898 | CTTCACTGTATAGAA[A/G]AGGAAGCAGTCCAGG | 10580 |
rs565417466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423179 | TGTCCTTGATCTAAC[C/T]CAGGGGTCCACAGAC | 10580 |
rs565429054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331349 | ACATGGGCAACTGAC[C/T]CAATGTGAAACAGTT | 10580 |
rs565441966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450451 | TGGGAAAAGACTTCT[C/T]GTAAGATTAGGTGAC | 10580 |
rs565444115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501606 | GGGTCTGTAGTCCCA[A/G]CTCCTCGGGAGGCTG | 10580 |
rs565446455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318161 | CCACACCATCATAAT[A/G]GCAACACAGACTGGT | 10580 |
rs565473852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401549 | CTTTAAGAAAGGAAC[A/G]GGTGCAGACTGCTGG | 10580 |
rs565493114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430611 | TTTGCTGCCAGAGGA[C/T]GGGACAGTTGGTTTG | 10580 |
rs565495747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359498 | ACGTTGCCCTCTAAA[A/G]GTGCTGGGATTACAG | 10580 |
rs565504923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509293 | TAGGGTTGTATATTT[C/T]CTCTACACTCTTACT | 10580 |
rs565517557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478808 | TAGGGTGCAAGGAAG[A/G]CTGCCACTTAGGATA | 10580 |
rs565517660 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552141 | CGCAGTGGCTCACAC[A/C]CGTAATCCCAGCATT | 10580 |
rs565518678 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337976 | GTTTAATGCTTTCTG[A/C]CAAGAACCCTCTACT | 10580 |
rs565535092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318721 | TATCTAGAGCACTTC[A/C]TACTCTACTCTGACC | 10580 |
rs565542295 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493756 | AGTGGGCAGGTTCCT[A/G]AGTATGGCTGAAAAT | 10580 |
rs565550946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529089 | TTGAAACCTTTGGCT[A/C]CCATGTTAGACAATG | 10580 |
rs565558690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424435 | CATCTGTTAATTCAA[C/T]CAACCGTGGATCAAA | 10580 |
rs565570885 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365154 | CATTTGCCACTTGGC[C/G]TTTTCATTTACTAAC | 10580 |
rs565577030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457681 | TGCATGGAGACAAGG[A/G]CATTGCCAGGAATGA | 10580 |
rs565578879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494534 | GCAAAGATGACAGAC[A/G]GATCGGAGTAAACCG | 10580 |
rs565596544 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371124 | CCTTTAAGGAAGATG[C/T]CAAGCTCAAAAGAAA | 10580 |
rs565648106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471007 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 10580 |
rs565652323 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328373 | AAACAACTAGTTCAA[C/T]TGCTTACCATCTAGA | 10580 |
rs565652344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372337 | AACTTAAGAAAAGAC[A/G]GGGGGGAAAAAAGAA | 10580 |
rs565653726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471594 | GGGCATGGTGGTACA[C/T]GCCTGTAGTCCAAGC | 10580 |
rs565659875 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365770 | CCTTCTCCAAGGTGG[A/G]AACTGTCCCCTAAGG | 10580 |
rs565681330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522133 | GCTCAGAGCCAGGTG[C/T]CAGTGTGGTTCTATA | 10580 |
rs565709505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477702 | GGAATGGAGTCAAAG[A/C]TGAACAAAGGACAGC | 10580 |
rs565712411 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443019 | AAAGTACAAGTCTTG[C/T]ACATACCTCGACTAA | 10580 |
rs565716550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486257 | ATGGGTTTGGATTGC[G/T]TTTTAATTTGTCTGA | 10580 |
rs565731420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388294 | CTACACCTTCTATTA[A/G]TAGTTGCTGTTCCTT | 10580 |
rs565733310 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532089 | GGAAGGCAAAAGGGG[A/G]TGGTTACTCTCTTGG | 10580 |
rs565756684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516302 | GCCTTCCAGGTCATT[C/G]TGATCCAGCTCAAGT | 10580 |
rs565759484 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430025 | AATTCTTCCGAGTAC[A/C]GTATTTGCATTTTAA | 10580 |
rs565766557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495628 | GGGTCTTTGTTTGAT[A/G]GCTCACTGTATCCCA | 10580 |
rs565815616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354492 | TTGTGCCAACAGAGG[G/T]GTGGGCAGTATTGGA | 10580 |
rs565818968 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502145 | CACCTCCACCTCAAA[A/G]CAGTACAAAAGAGCA | 10580 |
rs565824820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502803 | TTCAAAATCCTTTCT[C/G]CTTCTCTACCACTTG | 10580 |
rs565832403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510239 | TTTTATGTATGCATA[C/T]ATGTATATTCGTGTA | 10580 |
rs565837370 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366065 | ATCTGTCAAAAAAAA[A/T]CCTTATACACTCAGC | 10580 |
rs565847603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549276 | TCTAATTAATTTCAA[C/T]AGCCACATGTGGCTA | 10580 |
rs565875875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401990 | AAGGCCTTCTGTTGA[A/G]TGTGAGCAGAAAGGA | 10580 |
rs565879834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509763 | CTATCAAATGTGGAA[A/G]TAAATATCAAAAGAA | 10580 |
rs565882349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318762 | AAGCAGTGGTCCCCA[A/G]CCTTTTAGGCACCAG | 10580 |
rs565902886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347715 | TGCTGGGATTACAGG[C/T]GTGAACCACTACGCC | 10580 |
rs565944301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340904 | GGAGTGCAGTGGAGC[A/G]ATCTCAGCTCACTGC | 10580 |
rs565953821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433474 | ACACGCAGAGTGTTT[C/T]TTTATGTGCAGCTGA | 10580 |
rs565960119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416737 | CAGATGTCTTAATTG[A/G]GTCACTGAGATTTAG | 10580 |
rs565975343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480509 | GCATTTGGAGTCAGA[C/G]GAGGTGAACTTGAGT | 10580 |
rs565977638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375710 | TTGTTAGTGGGGGGA[A/G]GTCTAAGACAAGCAA | 10580 |
rs565990215 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435440 | TGGGACGTGGTGAAG[C/G]CTACCGCTCGAACAT | 10580 |
rs565995945 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312900 | CGGTGAAATGCTGCC[A/G]TGCAAATTGCACGTG | 10580 |
rs566003572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530675 | TCCCCTGTGAATACC[C/G]CAACACACCTGTGGT | 10580 |
rs566008091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517958 | TGAAGCAAAATGGCA[C/G]AGGAATCCAGGCAGG | 10580 |
rs566010423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511170 | CCTTATTTTTAAGTT[A/C]TAAACTGAAATACAA | 10580 |
rs566021740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417378 | CGCGATCTCGGCTCA[C/T]TGCAACCTCCGCCTC | 10580 |
rs566024158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409800 | AAACAGCTTGAAAAC[C/T]TTACATTTCATGCTG | 10580 |
rs566027591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496045 | TCCTCCTGCCTCAGC[A/C]TCCTAAGTAGCTGGG | 10580 |
rs566044644 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364238 | TATTCCTGCCAAGTA[-/T]TTTCATGAGAGCTGA | 10580 |
rs566057505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382119 | CCTTGCTTCGCTCTA[C/T]GGGCTTTTCATTCCA | 10580 |
rs566060293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396234 | TGATTTGGAAGTGCT[C/G]CTCTTTCAGCTTGAG | 10580 |
rs566069051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536907 | CAAGGTCATCCTACT[A/G]TATAGAATAAATCCA | 10580 |
rs566069925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517425 | GCTCACTTGCCGCTT[C/G]TTTGGGAACCTTCCT | 10580 |
rs566070691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544198 | CAAGCCCAAGAAGGA[C/T]GGCGAGCTCTCCTTC | 10580 |
rs566073502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395814 | ACTCTTCATTGGAAA[C/T]GCTAAACGCCTCAAT | 10580 |
rs566101436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438937 | CCCTCAGGGCCTCAG[C/T]TTTTCCATCTGTGTA | 10580 |
rs566127840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523733 | ACCATCCCTTAAACA[C/T]ACATGAATTGTGCCC | 10580 |
rs566133200 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534168 | GAGTGCAGTGGCGTG[A/G]TCTCGGCTCACCGCA | 10580 |
rs566137063 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95404893 | TGAGGCAGCACCAGA[C/T]CCAGGATTCAAAGCA | 10580 |
rs566168642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479949 | CAAAATGGTTCGGAG[A/T]CATGCCCACTCTCTC | 10580 |
rs566172178 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486968 | AAGTCTCCAGGGGCA[C/T]AGGAAGATCCCATAC | 10580 |
rs566177885 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498877 | CACAGGACTACATAC[A/T]CATGTGCACACACAC | 10580 |
rs566180364 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363577 | TTGAAATGAAAGTAA[A/T]GAGTAGTTACCACTA | 10580 |
rs566181639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538314 | GTGTTACAGAGGGAG[C/T]GGCTGCGCTGGGGCA | 10580 |
rs566188290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513180 | AGTTCTGCCTGCCCT[A/G]GGTCTTGACGCAGTG | 10580 |
rs566188331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367104 | ACTGGAGTGCAGTGG[C/T]ACAATCTCAGCTCAC | 10580 |
rs566212241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411390 | TGACAAAGATCCCTA[A/G]GACTTGTGAGAATCC | 10580 |
rs566249678 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541661 | CCCAACATGCCCAAC[C/T]CCCAGAAACCAGTCT | 10580 |
rs566316008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466481 | ACTTCCCAAATTCCA[A/G]CTTTTCAGGAACTAG | 10580 |
rs566323927 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509130 | AATCCAGCTGGGTCC[C/T]CCACACACTGCCTCA | 10580 |
rs566324090 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459671 | GTCCTTTCAACGGGG[A/G/T]AAACCCTTCCGTGGC | 10580 |
rs566350731 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534742 | CAAGGGAGGGGGCCA[A/G]AGCTGAAGAAAGCAC | 10580 |
rs566351295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433173 | TGGCGAGAAAGCTCA[C/T]GAGTGACAGTCTCAC | 10580 |
rs566360588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431981 | CCAGGAGCAAGATCA[C/T]TGAGTCATCCACACT | 10580 |
rs566377486 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473869 | ACATGGTCAATTTTG[A/T]ATATCACCTACTTAT | 10580 |
rs566381213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557487 | ATTTACAAAAAAACC[A/G]GGACTTCAGCAGAAC | 10580 |
rs566405287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320486 | GGGAGTTCAGGTGAT[G/T]CTCCTGCCTCAGCCT | 10580 |
rs566412476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524829 | GCATAGTGCCTGGCA[C/T]ATAATGGGCACATAA | 10580 |
rs566416874 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393429 | CTTTACCAATGATGA[A/G]AAGGGCTGAGAGGGA | 10580 |
rs566429018 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439657 | GGTGCACGGCCTCTT[C/T]GCACACAGCAAAAGC | 10580 |
rs566431211 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502014 | GAATGTTGGACAGGC[A/G]GCTCACACAGATCGA | 10580 |
rs566441732 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513475 | TGCAGATTTTTGATA[-/AT]GTTTTCACAGCCAGT | 10580 |
rs566458243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545012 | TCACTAATGTACCAC[A/G]TCCAACATAGAGGCC | 10580 |
rs566505000 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550673 | CTTCTTGAGAATATA[A/C]TCTATATCAGGCACA | 10580 |
rs566509843 | in-del | -/CGTG | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441464 | AGCTACACGAGTGCA[-/CGTG]CGTGGTTTAAAGAGA | 10580 |
rs566516594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342445 | AATTCCATTACTTTT[G/T]TTCATGAGACGGTCT | 10580 |
rs566542940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328962 | TACAAATGAGAAAAC[A/G]AAGACCTGCCGTGTG | 10580 |
rs566543544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419277 | AAAACAAAATGAATA[A/G]CCCCTCTCTAGTATT | 10580 |
rs566551909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505429 | GCCTCCAGTGTCAGA[A/C]GGAATACAGGGATCC | 10580 |
rs566570277 | snp | A/G | 0.000125287 | 0.00791376 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367728 | AAAAAGAAAAAAAAG[A/G]AGAAAAAAATAATGT | 10580 |
rs566574709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319890 | TGCTGTCTCCTACTC[A/G]ATTTGGAGTCTCCTA | 10580 |
rs566578596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551969 | GTTTTAAAATTATAA[A/G]CTTGCTCCAGGAAGT | 10580 |
rs566609692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320879 | CAGAGGTCACCAGGG[A/G]TTTTTCCAGTTGCCA | 10580 |
rs566609930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433676 | GCAAAGCCTCTTCTT[A/T]CCTTTCCTTCCACGC | 10580 |
rs566610266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427495 | CCAAAAACCAAGGTC[C/T]ACATTCAGAGATGAG | 10580 |
rs566618264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336035 | TAGCAAACAAAGGCC[C/T]CGCGCTCCCACACAA | 10580 |
rs566622090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440125 | AAATCCCAATGAACT[A/G]GTGTTTTTATTATGT | 10580 |
rs566638557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350199 | AGAAAAATAAATAAA[A/C]AATAAAATAAAAAAG | 10580 |
rs566640460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95490067 | ATATCTCACCTAAGA[A/C]CTCCAACATCCACTA | 10580 |
rs566673851 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536868 | TAGTCACATTGGGAC[A/G]AAGCACCCTGGGAAA | 10580 |
rs566676901 | snp | C/T | 0.000735384 | 0.0191612 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356775 | CTGTCATAATCCCGT[C/T]GGGAGCGCATGAGCA | 10580 |
rs566686164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497479 | CCATTCAGCCATCCT[C/T]AGCTTGAAAAATTCA | 10580 |
rs566703365 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489511 | CCTGTCCTCATGGAG[C/T]TCACATTCTTATGTA | 10580 |
rs566732582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467570 | TCCCACTAACCAAGA[C/G]GCGGGGGTCCATTTG | 10580 |
rs566736989 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460892 | AACTGAATGAATATT[A/G]TCTTTACTTTTACCC | 10580 |
rs566758182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357405 | AGAGAGAGAAATCTT[C/G]AAGGAGAACAAGGTT | 10580 |
rs566763509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518699 | GCTTTCTGGTAGGGA[C/G]GGAAGGAATGACAGA | 10580 |
rs566767448 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542536 | AATTACACCTTATCT[A/C]GCCATACTCTTTGTG | 10580 |
rs566771883 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366177 | ACAAGACACAGATGC[A/G]ATGGTGACAAAATAA | 10580 |
rs566779038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482330 | TGGCTTTGGACCCAC[C/T]ACAAAAAAAAATTAA | 10580 |
rs566800226 | in-del | -/T | 0.290718 | 0.246662 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343290 | CTTTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTGA | 10580 |
rs566813864 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324487 | TGTCCTTTTGGGAAG[-/C]CTCCTCAAGTTCTCC | 10580 |
rs566824030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397691 | ATTATTCAACAGCAA[C/T]GTATCCGAGTCACCT | 10580 |
rs566832041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462411 | ACTAAACATCTGAAA[A/C]TGAAATAAAAAGATC | 10580 |
rs566834648 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540958 | CCTGAGATGGGCTGG[C/T]TGAGTCAGGACAGCC | 10580 |
rs566836848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475283 | GCCTTAATATCTTCA[C/T]GCCCTCGATAAATGT | 10580 |
rs566858652 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377453 | AATCTTTAGCATTAC[G/T]TTCACTTTTGCTACA | 10580 |
rs566866120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420924 | GAGTTCGGGGAACAC[C/T]TTCACAGAAGGAAGG | 10580 |
rs566876305 | in-del | -/ATTA | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527433 | TCTGTCTCAAAAATG[-/ATTA]ATTAATTAAGAATTT | 10580 |
rs566897054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420384 | TAGTGGAAGAGGACA[C/T]GCTTCTACATTTGCT | 10580 |
rs566924372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363265 | TCCTTGCATATCTGG[G/T]GCCTTGCATGGTTGT | 10580 |
rs566932454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546840 | CTCCTGGGTTCAAGC[A/G]ATTCTCATCCCTCAG | 10580 |
rs566936189 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494538 | AGATGACAGACGGAT[A/C]GGAGTAAACCGGCTC | 10580 |
rs566945549 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515305 | TCAATTCAGGGCTAT[C/T]GTGTGGCCAGACAGA | 10580 |
rs566958290 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513653 | AGAGGGAAAGCAGGA[G/T]TGCAAGGATGGCAGG | 10580 |
rs566986235 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343641 | ACATTTTCTTGAATT[-/A]AAAAAAAAATGACCT | 10580 |
rs567004866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519346 | GCACACAGACCAGTG[C/T]TGCCACCAGCACCTG | 10580 |
rs567017065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550482 | TCTCCCTCCCAGTGC[A/G]TCTTATCCTCCACTG | 10580 |
rs567026328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484565 | TGTTTTGTGGCCAGC[C/T]AGCTTGCAATCTGGC | 10580 |
rs567033810 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318580 | TTATTGACTATTTCC[C/T]TAATAACTTAGCATT | 10580 |
rs567093022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506706 | TGCTTCATAAAACCA[C/T]TTCTAATGAGACTTA | 10580 |
rs567094729 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514159 | CATCCTCGGGAGACA[C/G]AGGAAGAATGCCGTT | 10580 |
rs567108482 | snp | C/T | 4.9788e-05 | 0.00498914 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371334 | GAAATACCTGTGGCA[C/T]GTTTGCACTGGGTGC | 10580 |
rs567113862 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442425 | GCGTGGTGGGAGGTG[C/T]TTGGATCATGGGGGT | 10580 |
rs567146661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393718 | TACATGTCCTATTCA[C/T]GGCATTACTTCCAAC | 10580 |
rs567160876 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439478 | GTTCTGCCACTGGAC[A/G]AGAAAGTAGCTTTAG | 10580 |
rs567173144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372128 | CTGGCTCAAACAAGG[A/G]GGGGTACACTGGGAG | 10580 |
rs567197930 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441522 | TTAGGAGAAAGAGGT[-/A]AAAATCACAACACAA | 10580 |
rs567202354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406552 | AGTGACCGTCTCCTG[A/G]GAGCTTGCTAAATGC | 10580 |
rs567210038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515556 | TTTAAAAAGTTGTCT[A/G]TCTCAACTAAGAAAG | 10580 |
rs567221082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344601 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 10580 |
rs567228737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434908 | CCAAGACAACAGACC[A/C]CTCCCCTCTAACTAT | 10580 |
rs567230572 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470418 | TTCACAGCAAAACAC[G/T]TAATGCAAAATAGAG | 10580 |
rs567249934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384959 | AGACCCATCGTCAAA[C/T]GGCTTCCTCTGCAAA | 10580 |
rs567259646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534228 | CCTGCCTCAGCCTCC[C/T]GAGTCGCTGGGATTA | 10580 |
rs567259808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337568 | GAGGTGTGGAGATGG[A/G]GAGAGGTTCCCGTCA | 10580 |
rs567298645 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505601 | TACTCTCAGCTGGAA[C/T]AGTATCAACTCCATT | 10580 |
rs567316083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401074 | GGTAATTCAAGAGGT[C/G]AAAGGATTAGGGACA | 10580 |
rs567319630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527403 | TGCACCCCAGCCTGA[A/G]CAACGGGGTGAGACT | 10580 |
rs567322112 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316033 | AGAGAACTGAGATGG[C/T]AGGGTCCAGAGATAA | 10580 |
rs567346013 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363205 | CAAATCTGTCTCCCC[C/T]ATTACACCTGGAACC | 10580 |
rs567354572 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441416 | GTGCTGATGTTATCC[A/G]ACATCCCTTTCAAAC | 10580 |
rs567373270 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341072 | TCTCAAACGCCTGAC[C/T]TCAAGTGATCTACCC | 10580 |
rs567389121 | snp | A/C | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392956 | TCTGCATGCTCTGTG[A/C]TTGTTGCCTTGAAGG | 10580 |
rs567390148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95408133 | TGTGTCCGTAAGTCT[A/G]GGAACCTCTGAGCTC | 10580 |
rs567394798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464275 | AGTGAGCAGAGATGG[C/T]GCCACTGCACTCCAG | 10580 |
rs567396181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534800 | AAGGCAAACACAGAG[A/G]AGAAAGTGAAAAGCA | 10580 |
rs567434554 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560823 | CTCCATCCCGCCGCT[C/T]GCTCCCTCCGCCTTC | 10580 |
rs567436480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463414 | AGCCCCATGAGCAGA[C/T]ACAAGTGATCCCTTC | 10580 |
rs567451580 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409009 | GAGAAAGGCAAGAAC[A/C]AAAGGCATTTGGGTA | 10580 |
rs567462351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415010 | ATGAGACAGTCGGAG[C/T]TGGCCAGCTGGCCTT | 10580 |
rs567466997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470921 | GCAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10580 |
rs567473171 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403377 | TCTCTTTCAGGAGCT[A/C]CTGAACAAAGCTGTA | 10580 |
rs567499139 | in-del | -/TTGACAGAGGAGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412425 | CAGAGGCTCCTCCTC[-/TTGACAGAGGAGG]AAGAGGAATCCAAGT | 10580 |
rs567503283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364266 | TGAAAAACAGAGGCT[C/T]TGAAGACCTATTTTC | 10580 |
rs567512337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536306 | ACATCAAGCACATTC[A/G]TAACCTATTTTGAAT | 10580 |
rs567513793 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428834 | AGGGAGGGAGCCAGA[C/T]GCCATCTGACATTAG | 10580 |
rs567525873 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358714 | CAGACATGCGCGCGC[A/G]CGCGCGCGCACACAC | 10580 |
rs567543198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430671 | CACATTAAAGCCTTT[C/T]TCTTTGCATCATCCC | 10580 |
rs567567438 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561555 | CAGCCGTGACAGGAA[A/G]GGGCGTGTGCGCGGA | 10580 |
rs567570207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563415 | ACCTGAGCTCAGGAG[C/T]TTGAGACCAGCCTGG | 10580 |
rs567584487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529814 | AAATAAGAATAGATG[A/C]CTCACATTATAACCC | 10580 |
rs567595932 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330675 | ACCACCACGCCCGGC[A/T]AATTTTTCTATTTTT | 10580 |
rs567610569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500966 | TCAACACCTGCACAC[G/T]GCCGGCCCTTCTTCC | 10580 |
rs567632064 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371283 | AAGAAAACAAAGCAC[A/C]GCTTGAAAAGGAACT | 10580 |
rs567633139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449944 | TAATCATACTAATTG[C/T]CAAGAAAAATATTTT | 10580 |
rs567639963 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395715 | AGGAAGTGATGAGTG[C/G]AGATGACCCCATCTG | 10580 |
rs567652266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501847 | CCTGAACATTCTGAG[C/T]GTCAGTCTTCTGGAT | 10580 |
rs567664715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364743 | AGACGTGAGCCACCA[C/T]GCCAGGTCTAAATTG | 10580 |
rs567684131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443313 | ATACAAAAAGCAGCC[A/G]GGTGTGGTGGTGGGT | 10580 |
rs567695277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317612 | GAATGTCTACACGTA[C/T]GCCTGAGTTTCATGG | 10580 |
rs567700264 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394048 | AGCTCTTTCATTAAA[C/T]GTTTTCCAGCTTAGC | 10580 |
rs567701993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555227 | GGGAGAAGGCATCAG[C/T]CAGGAAACGCAGAAA | 10580 |
rs567702613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317015 | CAAAGTAGTGAGGGC[C/T]GTGGGCTTCTGAGGA | 10580 |
rs567715129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324660 | CGACCTTGTATGGCT[C/G]CAACACCACCCACCC | 10580 |
rs567720538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437325 | GAAATGCAACAACAG[G/T]CTCCAGGTCTCAGAA | 10580 |
rs567735270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318882 | TTCTCATAAGGAAGG[A/C]GTAACCTAGATCCCT | 10580 |
rs567736906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387185 | AGAAATCTCACCCAC[A/G]CCAGGCTAACACAGG | 10580 |
rs567744136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493981 | CATCCTCCAGGAAAG[A/G]GCCAAGGATCCAGAT | 10580 |
rs567753430 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447875 | CACGAAGTTTCTGTA[A/T]AAAGACCAATGTTTC | 10580 |
rs567759486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339775 | TCACCCATCACATAG[A/T]CATTTGGGGATAAAC | 10580 |
rs567760222 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497959 | CTACCTTGTTTTCTC[A/G]GTGACAATTCCCATT | 10580 |
rs567765124 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563027 | GCTATGCACCGTACT[A/G]TACTTGTGCTAAGAG | 10580 |
rs567765605 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542336 | TACCAAGAGGATGCT[A/C]AATGAGTGGCTTTCA | 10580 |
rs567791904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95319523 | ACATAAGAGGCACCT[A/G]CTATGTACCAACTTC | 10580 |
rs567817095 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556644 | AAGCTCCGCCTCCCA[A/G]GTTCATGCCATTCTC | 10580 |
rs567817520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556740 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10580 |
rs567890786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550549 | ATGTCTATCTCAGAA[C/T]AAGCGACGGATTTAT | 10580 |
rs567892283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485648 | CAATCAGAATGATTT[C/T]TTCCCATGACGAGCA | 10580 |
rs567898296 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326633 | CACCCTCAGTGGAAA[G/T]GGAAACCATTACTAT | 10580 |
rs567902084 | snp | A/G | 0.000165158 | 0.0090858 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394582 | TAGCAGCACCAGTAC[A/G]GAGAGGCACACAATT | 10580 |
rs567905800 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399996 | GCTTACAGTCTAGTG[A/G]GCAGAAAAACCAAGT | 10580 |
rs567920311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522873 | GCAATCCAACAACTA[C/T]ACTTCTCCTTTCCCC | 10580 |
rs567938438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353561 | GCTGGTGTGTAATGG[C/T]GCCATCTCGGCTCAC | 10580 |
rs567938506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346107 | TAAGACCCCAACCTC[G/T]GCCTAGGTTTGAATT | 10580 |
rs567945231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465445 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA | 10580 |
rs567946544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436695 | CTGGGATGAGCGTTC[A/G]TTCCAATTCTGAATT | 10580 |
rs567952103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355026 | TGGAAACCAGCTTGC[A/G]AAAAGAGTTCACCTT | 10580 |
rs567953725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347748 | GCTGTGGAATTTCTT[A/T]CTTTTTTTTGAGACA | 10580 |
rs567954088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557311 | AGAAGCTCCCCCAAA[G/T]GAGCTACAATTCAGT | 10580 |
rs567961617 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473687 | CATATAATATATATA[C/T]ACACACACACATACA | 10580 |
rs567966583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386706 | CGGAAAAAAACAGCA[C/T]TACTTGGGAAGTTTA | 10580 |
rs567967302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95478855 | GCCAAGCAGTGTGAT[A/G]GCTGACACCTTAGAA | 10580 |
rs567971137 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418181 | CTCCCAGGTTCAAGC[A/T]ATTCTCCTGCCTCAG | 10580 |
rs567971973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417445 | GTAGCTGAGACTATA[A/G]GCACATGCCACCATG | 10580 |
rs568011805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365606 | TTAGAGCTGAAGGCC[C/T]GGCTCAATTGGAAGC | 10580 |
rs568011827 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562809 | ATCTGGAAGCTTACT[C/T]TATAAATGAGAAAAC | 10580 |
rs568012705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366172 | AAAGAACAAGACACA[A/G]ATGCGATGGTGACAA | 10580 |
rs568022980 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386541 | CTTGGGAGGCTAAGG[C/T]AGAAGAATTGCTTGA | 10580 |
rs568023222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451324 | ACACACAAACTACCC[C/T]CATTGCTCCCAGTGC | 10580 |
rs568050717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332583 | AGGATTACAGGCATG[A/C]ACCACCACACTCAGC | 10580 |
rs568055798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516361 | AATAACATGAACCAC[A/G]GTGGTAGATCAACAA | 10580 |
rs568083605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480743 | GCATGCCAGGTCCTC[A/C]GCTGGGTACGAGGCA | 10580 |
rs568084133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476030 | CTGCGCTCCAGGCTC[C/T]GTGTTCTAAAACACT | 10580 |
rs568092250 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471615 | TAGTCCAAGCTACTT[G/T]GGAGGCTGAGCAGGA | 10580 |
rs568105093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479655 | GGTGATGGGGAGAGA[A/G]GTCAGATGATCCGTG | 10580 |
rs568109954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516722 | ACAACAGGGGTGAAA[C/T]TGACTTTCTTTTCAT | 10580 |
rs568154676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375275 | TTCTCCCTTCTATTT[C/T]ATATTCCTTTGGGTG | 10580 |
rs568163968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95373041 | TTGTGAAATTTTGAC[C/T]TGCTCTTACATATAG | 10580 |
rs568184236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381339 | TTAAAAAAAACTGGA[C/T]TTCAGTCCACTTAAT | 10580 |
rs568191093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348326 | TAGAAAAACACAAGG[A/G]AGTAGGTTACCTCAT | 10580 |
rs568195665 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445710 | GGCTCGGCAGTGGTT[G/T]TGTCTCTACAACCTT | 10580 |
rs568195957 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416882 | AGAAGGAAGACAAGC[A/G]TGAGATTAAAAGCAC | 10580 |
rs568217686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445177 | CCAGCTCTTGCACAC[A/G]AGGACTTTTTGAGTA | 10580 |
rs568218180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537615 | CTCCATTAATCTGTA[C/T]GAGATCAAAGGAGAA | 10580 |
rs568243369 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542111 | CTCCAATAGACCCAG[A/G]AAGTTCTTGTCCATG | 10580 |
rs568245056 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519983 | TTAAGTGGACCACCA[C/T]AAATACCAGACACAG | 10580 |
rs568266894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497409 | CCCCAATTGTTCAGA[C/T]CTGGGTATTTCCCAG | 10580 |
rs568275550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359898 | CCTATTTCAGGGGAC[A/T]GCCGAGGGTGGGGGT | 10580 |
rs568278238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367791 | CAAGAGGAAAAAGAG[A/C]GAGGTCAATTTCTTT | 10580 |
rs568281402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544278 | CCCTCTGAGGCAGTG[A/G]CTCAGCCCTGCTACT | 10580 |
rs568282183 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522922 | GACAGGACTTCAGAA[C/T]GTCTGGAGACCCTCC | 10580 |
rs568286919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550092 | AGATACAGAGGATGG[C/T]GACGTGATACTCACA | 10580 |
rs568303918 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311547 | CATATTTTAGAAATA[A/T]TGGCAAAATGGTCAA | 10580 |
rs568340192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95382165 | TTCCCATTCACACTA[C/G]AGCAGTGAGAGAGAA | 10580 |
rs568351102 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452635 | AGCAAAAATTCAATG[A/G]AAGTATTTTTTTAAA | 10580 |
rs568389221 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450442 | CATACAACATGGGAA[A/G]AGACTTCTCGTAAGA | 10580 |
rs568394558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488642 | TCTCAAACCTAAGAC[A/G]GCCCAACAGAACCCT | 10580 |
rs568402718 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538960 | GAGTGGACCCCAACC[A/C]CCTCTCACCTGCTGC | 10580 |
rs568415697 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509789 | AAGAATCAGCTAAGA[G/T]TTTAAAGTGGCTGCC | 10580 |
rs568421178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390455 | GTGTTCAGAGTAGGG[A/G]GCGCTAATTCTATAA | 10580 |
rs568426231 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487532 | ACAAAGGCAGTCAGA[C/T]GGAGGAAGGCTCACA | 10580 |
rs568426763 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481259 | CTAGCTCCACCTGCC[A/G]CCCTACACATCCAGG | 10580 |
rs568435414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538127 | CAAAAAAAAAAAAAG[A/G]TGCTTGTGAAGGGAC | 10580 |
rs568447297 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542491 | TCAAATGACCTCTTA[C/T]CATTCTTCCAAAATT | 10580 |
rs568459492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438967 | AATGAGGGTGGCAAA[C/T]CACGCCCCACCTGTG | 10580 |
rs568463513 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455715 | CGAGGTGGGTGGATC[A/G]CTTGAGCCCAGGAGT | 10580 |
rs568465996 | snp | A/C | 0.000614849 | 0.0175227 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432410 | TCCTCCCGCCCTTCC[A/C]ACGTGGCTTTGAACA | 10580 |
rs568471183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497539 | GACGTCAAGACCCTC[A/C]AGAATCTGACCCAAG | 10580 |
rs568479598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389237 | TCATACATGACCCCC[A/G]TGAACAAAAATAGTA | 10580 |
rs568523501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396327 | GCTGGGGCAGATTAT[C/T]GTTCGTATTAACACA | 10580 |
rs568527765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514106 | CTTGAACATTGACTA[C/T]TATGTAGAAAAAAAG | 10580 |
rs568533476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524846 | TAATGGGCACATAAT[A/G]AACATCTGGTGAGTA | 10580 |
rs568540728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460278 | AAATCTTATTTCTTC[C/T]ATCACTGAAGTCTAC | 10580 |
rs568542855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466614 | GAAGCATGTGCACAC[A/G]AAAGAGAGCTCGTTA | 10580 |
rs568581528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532762 | CCATTGCACAACTCC[A/G]GGGGGCATGATTCAC | 10580 |
rs568587086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361485 | CAACAATGCTGTGTC[A/G]CCCAGGCTGGAGTGC | 10580 |
rs568589815 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95550075 | ACTGTGATAGACACA[A/G]GAGATACAGAGGATG | 10580 |
rs568610152 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506860 | GTAACAGCTGCATGG[-/T]TTTTTTTGTTGTTGT | 10580 |
rs568611473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95498468 | AAACCTTTGTGAATA[C/T]ACTTAAAAAAACTGT | 10580 |
rs568619730 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447622 | CACTAGCAGAGCCAC[A/G]TTTCTCCAATTTTTC | 10580 |
rs568633139 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382411 | ACCATAATTGCATTC[C/T]TCCCTGTTCCACACT | 10580 |
rs568681148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420042 | AATGGCTGATTTTAC[A/T]TTGAATATAAAGGAT | 10580 |
rs568704380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533270 | GCAAAACATAGCCAA[C/T]CTGACTTAGGGTTTC | 10580 |
rs568714282 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378993 | TCAAGCCTGTAGTCC[C/T]AGCAGTTTGGGAGGC | 10580 |
rs568724708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335056 | TCTAGCAAAAGGCTA[A/C]GCCTGATTTCTTATA | 10580 |
rs568748075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352538 | GTGGGATTTCCAGTA[C/T]TCAAATAAGTTGTAA | 10580 |
rs568754436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426685 | AGGCAACAGAAGCTC[C/T]GCATTTGGTACCTTT | 10580 |
rs568754859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467405 | CCCTGAGGCGCTATT[C/G]AGCAAAGACAGCAAC | 10580 |
rs568755894 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368777 | CCCACGCCACCCCAA[A/T]TATTCCTCAGAGAGC | 10580 |
rs568757298 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387132 | CTCTAAAGAAAAAAA[-/G]AAACAAAAAACACTT | 10580 |
rs568762372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326952 | GATATACTGGGTTAC[A/C]ATATATTATTAAAAT | 10580 |
rs568781433 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518469 | GAGTAAGTCATTTCA[A/C]CTCCCTGGGCCCCAG | 10580 |
rs568809858 | snp | C/T | 0.000120707 | 0.00776782 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356197 | TTGAACAGCGGTCCA[C/T]GTCATCAGAGCAGGT | 10580 |
rs568820603 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348969 | ATCACCTGGGAAATT[A/G]TTAAAAATGTAAATT | 10580 |
rs568829347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392136 | ATAGAGCGCAGGGCC[A/C]CCTATCGGGGAGCAC | 10580 |
rs568830192 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323300 | GAAAAAGGGAATAAC[A/G]TTTTTGAAAACTTCC | 10580 |
rs568837491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446873 | AATCTAATCTTGGGC[C/T]GGGCTCAATGACTCA | 10580 |
rs568842269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525941 | TGGAATTTATGTCCC[A/G]GATGGAAGAACTAAA | 10580 |
rs568892208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95539285 | TCTGTTACGAGGAGC[C/T]ATCTTGTCCACTCTA | 10580 |
rs568904094 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447169 | AACAAACAAAAAAAA[A/C]CAAAAAAACCCAGTC | 10580 |
rs568926953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323656 | TAAATACCCTGAAGA[A/G]CCATCCTTGAAAAAA | 10580 |
rs568927980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321724 | ATTTGACATTCTACA[G/T]CAGTTAATCTTTACC | 10580 |
rs568967885 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547529 | CTGAGGTCAGGAGAC[C/G]AAGACCAGCATGGCC | 10580 |
rs568979390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453891 | GACCAATCTCTATAG[C/T]ATACTGACAGATAAC | 10580 |
rs568987257 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462718 | TTATACCACTGTGCA[A/T]CATGCAAACTTTTTT | 10580 |
rs568993028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433777 | CAGCACCTCTTGTAT[G/T]GAACGCAATGCACGA | 10580 |
rs569015177 | snp | A/G | 0.000337262 | 0.0129814 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384403 | CCTAGGGATCCCAGC[A/G]GACAGAAGAGTGAAG | 10580 |
rs569017684 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519720 | GGAAAGAAAGAGGGG[G/T]AGAAGGAAAAATACA | 10580 |
rs569026193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95519438 | ATAGGAGTCACAAAA[G/T]AACTGACATCCATTT | 10580 |
rs569028131 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346770 | AACAAACAAACAAAA[A/T]GACAAAGTCAGCCAG | 10580 |
rs569033362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553628 | GGTAGGAGGAGTGCT[C/T]CAGGCCAGGAGTTAA | 10580 |
rs569037008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343734 | GGTGTGCTCACTTTG[C/T]AGGATGCCAGGAAGT | 10580 |
rs569058282 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517701 | ACCAGAGCAGCTGGG[A/C]AGGGAAGAGGACGTT | 10580 |
rs569059273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421688 | AATGAATTCCCTCTT[G/T]CAGAACACTTCTACA | 10580 |
rs569059923 | in-del | -/T | 0.496937 | 0.0390173 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320381 | TCTTCCTTCACTTAC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs569106076 | in-del | -/AG | 0.0807149 | 0.183963 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344859 | TGAAAACACTGAGTT[-/AG]GAGGAAGGAGCCCTC | 10580 |
rs569106305 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392066 | TTGGTGCTGATCTGT[C/T]TTGAATGCCTTTCTT | 10580 |
rs569112727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459974 | TTCTGATCCTGCCTG[A/G]AAACAAAGTGTGGTT | 10580 |
rs569118400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344696 | AGGTGTGAGCTACCA[C/T]GCCTGGCCCCGACAG | 10580 |
rs569122609 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386671 | AGAAGAAGAAAATGA[A/G]AAATAGTTCTTATAA | 10580 |
rs569129825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440889 | ATAAAGAGAGGGCTA[A/T]TGTGCATGTAAAGTG | 10580 |
rs569137046 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442476 | CTATCTCTGCAATAG[C/T]GAGTTCTCACAAGAC | 10580 |
rs569161333 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421634 | TAAAGAATTTTTTTT[A/G]AAAACGTCTCAGACC | 10580 |
rs569165188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513706 | TAAATTCACCAGACA[C/T]GGGACACCTGGGCTG | 10580 |
rs569180928 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475333 | TTTTATAGCAAGTAC[C/G]ATGGGTTCTAGTTTC | 10580 |
rs569181578 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524512 | TAAACTTGATTGAGT[C/T]ACTTGTCTTTCTACT | 10580 |
rs569204290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559447 | AAAGGCCAACAAGGC[A/G]GGTATCGTCCACAAG | 10580 |
rs569213820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448433 | AAATTTCAATGGGGA[A/G]AAAAACTCCGCAGGG | 10580 |
rs569216246 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502772 | TCTTCAAAATCCCAA[C/T]GCACAGGAAAGTATC | 10580 |
rs569218301 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523355 | ACGGTGCATGGAACA[C/G/T]GGCTCTAAGCTCCCT | 10580 |
rs569223443 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326471 | CTCACTTAGCGTTTG[C/T]TGAATAAATGAAGGA | 10580 |
rs569255993 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543164 | GCATGTGCCGGTCCC[C/T]CTGTCCTCTGGTTGG | 10580 |
rs569281603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329797 | ATTTAGTTTCCTTGT[A/G]TTGAGAAGTGTTCCC | 10580 |
rs569289137 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399844 | GAGCACTAACAAAGA[C/T]ACCACATATGACCTA | 10580 |
rs569296402 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526436 | CCCCCCTCTCTCAGG[A/C]GCATCCAATGTGCAG | 10580 |
rs569302012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95413608 | GATCCTACTGAACCC[A/G]AAGCCCTGTGAGTAG | 10580 |
rs569303974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358107 | CTGCCTGGGGAAGAA[A/G]GGTTGGAGGAAGGAT | 10580 |
rs569314028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492530 | TGATCTGCAGTCAAA[C/T]GCTCTACCCCTGAGC | 10580 |
rs569319569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468285 | GGTAGTTCAGCAGCC[C/T]CCTCAGATCCCATGG | 10580 |
rs569342002 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95353703 | GAGATGGGGTTTCAC[-/TG]TGTTAGCCAGGATGG | 10580 |
rs569353526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369065 | CTCACCCAGCAACCT[C/G]CAAAGCCTTTGGAAA | 10580 |
rs569355501 | snp | A/G | 1.66418e-05 | 0.00288455 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95371422 | GAGATCTTTGTCTAG[A/G]TTAGTCTGGTTCAAG | 10580 |
rs569358624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507393 | ATCCCTTCATCAAAA[A/G]GAGCCTGATCTTCCC | 10580 |
rs569375005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369765 | CATTCTCACTCCAGG[A/G]CTAGTTGTGATCTCT | 10580 |
rs569376902 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436177 | CCACCCTCCCCCACA[C/T]GCCTTAAGTCTCTTG | 10580 |
rs569392802 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382320 | GTAAGGACTAAACAA[C/T]TTACATGAGACAGCA | 10580 |
rs569411368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95345265 | AAAGAAAATTGAGTG[A/G]GGGAGAAGTTGATAA | 10580 |
rs569422243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477498 | TAGAGAGAACACCAT[A/G]GGGAGAAGCAAAGTT | 10580 |
rs569423867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470340 | AAGAGACCTGGCCTG[C/T]ATGTCTTTGGAAAAC | 10580 |
rs569431297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500142 | TCCCGGAGAACGTGC[A/T]TGGAATGCAACTGTC | 10580 |
rs569456236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456275 | AGGTCTCCTCCAGGG[C/T]TCATGTTGAAATCTA | 10580 |
rs569478542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407742 | CCAGGGGATCAGGAC[C/T]AGCCTAGGCAACATG | 10580 |
rs569480679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364857 | AGAGTTTACTGCCAA[C/T]CCTAGTCCCTTGGCC | 10580 |
rs569492015 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95507876 | GATCATACCACTGCA[C/T]TCCAGCCTGGGTGAC | 10580 |
rs569502845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534965 | ATCTGTCTGTCTCCC[A/G]TAGCAAGAGACTCAA | 10580 |
rs569523276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357569 | AGGTTCACCACGGCC[A/G]ACGCTCAGTGAATGG | 10580 |
rs569523836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485406 | TAGTGAATGCTGAAT[A/T]ATCCAAAGTTCAACA | 10580 |
rs569525973 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386611 | CCTGTACTCCAGCCT[C/G]GCTGATGGAGTGAGA | 10580 |
rs569561788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470957 | TTGCTTGAACCCAGG[A/G]GGCAGAGGTTGCAGT | 10580 |
rs569564597 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429975 | TTACAAAGATGAACT[C/T]ACTGTAAGGTGTGAA | 10580 |
rs569568154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541279 | TTAGAAGAGGGATCT[G/T]GGGGCCCTCAACATA | 10580 |
rs569593496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380118 | TCTCCAAGAAGGCCC[C/G]GTGGGGCACTATGTG | 10580 |
rs569596011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399349 | GCCCATGGGCTGATT[C/T]TACTGGAACACAACC | 10580 |
rs569619395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372224 | GCTGCCTGCTGGAGC[A/G]GAAGCCTGAGGATTT | 10580 |
rs569674951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494678 | TTTCTGATTGCAAGG[A/C]CCAGCAGCAATCCAT | 10580 |
rs569678005 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95433357 | TTTTAGAGTTTCCTT[G/T]AGAAAGATTTCAAAA | 10580 |
rs569682467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422733 | CTTTTCTTCTTTCCA[C/T]TAAATGAGGCACATA | 10580 |
rs569703885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395181 | CTTGAATTCTGGAAC[A/G]TACTAAGCTTCACTA | 10580 |
rs569706484 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468198 | CACCGTGCCCAGCCC[-/T]TTACCATCTTCTAAC | 10580 |
rs569716178 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406583 | CAGGCGCTGTTTTAG[C/T]GCTTTTGCAAATAAC | 10580 |
rs569718772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393752 | AGTGCCTGGCACACA[G/T]CAAGTGTTCAATACT | 10580 |
rs569736398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502033 | CACACAGATCGATTC[A/G]ACTCCAGGAGGCACA | 10580 |
rs569737683 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562723 | TTAGATGTCAGGGAA[C/T]GGTGACAAGTCTTTG | 10580 |
rs569741871 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411522 | AATAAGACCCCAAAA[A/G]GTACTAAGAATATTT | 10580 |
rs569783519 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463583 | CCAAGTTTTGGAAAA[C/T]TTGGAAAGGGATTTT | 10580 |
rs569786126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508943 | ACCAGCGTGGAGGAA[A/G]CAGGATAAGCCCAGA | 10580 |
rs569787685 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436083 | TCAGGCCACCCTGAT[A/G]CCCTTCAGTCACTCC | 10580 |
rs569810393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457269 | ACTATGTATTCTATT[A/C]CAATCAGTGTAGGAT | 10580 |
rs569811325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331568 | CATCATTCTCTATGC[A/G]CACCTTTCATGGTCC | 10580 |
rs569812951 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551766 | CCCATGAAACAAGAA[C/T]AGAATGTCATCTAAA | 10580 |
rs569822223 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95437986 | CCAAGCCCAGAGTTA[A/T]CCAAGCTACAAACAT | 10580 |
rs569848569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95555320 | CGTGGAGTAGGGAAT[C/G]ACCGGGCATCTGGTG | 10580 |
rs569851099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95515760 | GATGATTTCTTTACA[G/T]AAGCCCAAGGGTGCT | 10580 |
rs569861816 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430449 | AGAGTAAACCCTGTC[A/T]CAAAAAAAGAAAACG | 10580 |
rs569878655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95416556 | CACCAGTGGGAGAAG[A/C]ACCAAAGCCCCCAAC | 10580 |
rs569896740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516264 | ATTCTGGGGGAGGGA[C/G]CCAGCAATCTGTGTC | 10580 |
rs569898647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324673 | CTCCAACACCACCCA[C/T]CCTCCACTCACTGCC | 10580 |
rs569905326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450024 | AAATCTATGAGAAAA[C/G]GTTTACTTAACCCAA | 10580 |
rs569941965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95423610 | CACTGCAGTCTCACT[A/G]CCCAATCCTCCGTTT | 10580 |
rs569968702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387311 | CAAGTCATACAGATT[C/T]ATCTGAACAACTATA | 10580 |
rs569974874 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457513 | CTTGACACACAGGAA[A/G]AACTCAGTAAATGGT | 10580 |
rs569989037 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489322 | CCAGCCCTTCACCTT[C/G]TTTTACTGTTTTCAT | 10580 |
rs570004366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415980 | AAGGAACCAGGGCAC[A/G]CCACACCTTTGGGAG | 10580 |
rs570022041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536856 | GGGCACTAGTAATAG[A/T]CACATTGGGACGAAG | 10580 |
rs570027388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543021 | GACTATGCCCATGCT[G/T]CAGGCAGGGGCCCAG | 10580 |
rs570028671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388166 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAT | 10580 |
rs570034555 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537489 | GCTAAACCTATCACA[C/T]GCCCCTGGGTAGAGC | 10580 |
rs570059385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523579 | AATACATTTAGCACA[C/T]GGTTGTAACCGTAGC | 10580 |
rs570076090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346848 | TACTTGCTTAAATTA[C/T]GATATGCAAGTAGGT | 10580 |
rs570078996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95401829 | TGTTAAGAACAGATT[C/G]GCTTTATGGAATGAG | 10580 |
rs570094241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444973 | TTTGCCACAAATGTC[C/T]ACCAACTGGAGCAGA | 10580 |
rs570097749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320437 | TAGGCTGGAGTGCAA[C/T]GGCGCAGTCTTGGTT | 10580 |
rs570100741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431421 | AAGTGTGAAAGTCAC[C/T]GCCCTACAGAGTGGA | 10580 |
rs570125184 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479892 | CCAGGGATGGGTCCA[G/T]AAACCAGCAGATATA | 10580 |
rs570130017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517339 | AAAGAAGGAAGGGTG[C/T]TGGGCTCAGGGGATG | 10580 |
rs570173315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508562 | CCGTCAAGAATGCTC[C/T]TATCCTCTGAAATGG | 10580 |
rs570189490 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487455 | TTCAAAGAAGGAAAT[G/T]GTGAGGATATTCAAA | 10580 |
rs570190014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417602 | CCACTGCACCCAGCC[C/T]AGGTTTTCTTTAATG | 10580 |
rs570196523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543584 | AGGAAAGCTAAGTCT[G/T]TCCTTTAGTTAAAGC | 10580 |
rs570222043 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456729 | GCTTTTTATAAGACC[-/A]AAAAAAAAAAAAGAA | 10580 |
rs570231208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550589 | ACTGTATGTTTGGGT[A/G]TCTTGAAATCTGATG | 10580 |
rs570275952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446299 | ATCATTCCATATTGT[A/C]CCCCCTACCCCGCCA | 10580 |
rs570283949 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531860 | CGACCTCTTAAGTTA[C/T]GTTTTATTATTTTAA | 10580 |
rs570297429 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334382 | GGGCAGCAGCCCTTT[C/T]CACACAAATGCCAGC | 10580 |
rs570306008 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561284 | CTGCCGCCGCCGAGC[C/G]GGCAAGCGCGGCCGG | 10580 |
rs570308759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511106 | GATGCAATGTGGAAC[A/T]AAGATCACATTCTTA | 10580 |
rs570317533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430840 | GGAGTCAGGGCTGGG[C/G]TCAGGGATGCAGGAC | 10580 |
rs570319851 | snp | A/G | 0.000280915 | 0.0118481 | missense | SORBS1 | GRCh38.p7 | 10:95341578 | CCTCGATGTAGGTGC[A/G]TGGGAAGATTCCCAC | 10580 |
rs570334561 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557410 | AAGCACCGATGAAAA[A/T]CCAAGGAGAAAATGC | 10580 |
rs570362124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347521 | CTCACTGTAACCTCT[A/G]CCTCCCAGGTTCAAG | 10580 |
rs570363887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411346 | TTATCCTATCCTACT[A/G]TGACATTTTTTTCAC | 10580 |
rs570364732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332707 | ATCCGCCTGCCTCAG[G/T]CTCCCAAAGTGCTGG | 10580 |
rs570379599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323756 | ACTTTGGGAGGCCAA[A/G]GCAGGAGGACTGCTT | 10580 |
rs570407014 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418356 | GTGCTGGGATTACAG[A/G]CGTCAGCCACAGCGC | 10580 |
rs570428279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367048 | GCAAATGAGATTTTT[C/T]TTCTTTCTTTTTTGG | 10580 |
rs570443896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510609 | TCTTTGCTTCTTACA[A/G]TACCATCAGTCAGTA | 10580 |
rs570488610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474064 | ATTCTGAAATGCTTA[A/G]AAAAAAAAACAAAAA | 10580 |
rs570491636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360636 | GCTGCCTGCCCATGT[C/T]GCTGGGTGAAGCTCT | 10580 |
rs570494733 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504605 | ACAAATCTTTTAACA[A/T]CTCAGTGGCTCAGTG | 10580 |
rs570509955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95473351 | AATATTGTAGATCAC[C/T]GGGCACGGTGGCTCA | 10580 |
rs570525909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348368 | GTAGAGCTGTGTGAA[C/G]TTTAAAAAATGTATA | 10580 |
rs570536960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335942 | AAACCTGGCATGGCT[A/G]TTCGAGGATACCCCA | 10580 |
rs570539858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459143 | ATAAGCTTTTTCTTC[C/T]GTAAGAATGTGAAGC | 10580 |
rs570549318 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511829 | AACTGCCCCAGAAGA[C/T]AAACCCAAAGCTATC | 10580 |
rs570565398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542907 | CATTTTTAAAGCATG[A/G]CCAGGCCCGATCCCT | 10580 |
rs570567461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95366247 | CTGGGTGCCCCAGGC[A/C]CTGTGAAGACTGGGG | 10580 |
rs570574080 | snp | C/T | 9.88435e-05 | 0.00702937 | missense | SORBS1 | GRCh38.p7 | 10:95410665 | AGCACAATAGTAGGA[C/T]TGACAATCGTTGTGG | 10580 |
rs570624595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537743 | TGCTGCTTCACCTGC[A/G]GTCACACAGCTAGTG | 10580 |
rs570626204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95496762 | TAATGGTTCTCTCTC[C/T]TCCCCTCCCTAAGAC | 10580 |
rs570627253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531667 | GGCAGCCCCCGTCCC[A/G]GGTCCACCCCCGAAG | 10580 |
rs570628785 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95403962 | AGGATTACCACCCTT[C/G]TTTCCCATATGAGGA | 10580 |
rs570634636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348912 | AGTCAACCTCTAGGG[C/T]AGTGATTCTCAAAAT | 10580 |
rs570643363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335185 | TAGTGTGTCTCAAGC[C/T]TCTGTGCTCCTGTGT | 10580 |
rs570655082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504499 | AGTGATTGCAGTTGG[A/T]GGCTCATAATCTAGA | 10580 |
rs570658370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396876 | GTCATGGGCTGACAC[A/G]GGGAGATGTACCTAA | 10580 |
rs570687392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461557 | TGTCATTTAGGGCTA[C/T]ACTTTGAGAAATGTT | 10580 |
rs570690308 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474225 | ATAAGAAATCCTTAA[A/G]AAAAATAAACATGGC | 10580 |
rs570690859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538235 | GGCAAGGTGAAGGCA[C/G]GGCCATAATTATGTG | 10580 |
rs570720206 | in-del | -/AA | 0.0923359 | 0.194016 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493289 | GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAGAA | 10580 |
rs570726369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453150 | AATTAGCCGGGTGTT[A/G]TGGTGCATGCCTGTA | 10580 |
rs570728490 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476349 | CTCAACAGGTGAAAT[-/A]ATTTGAGGAACATTG | 10580 |
rs570739677 | snp | A/T | 1.65704e-05 | 0.00287836 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95376049 | TCTTCTGGGCTTATA[A/T]CCCGACTCTATAGGG | 10580 |
rs570757733 | in-del | -/GGGCACGGGCGGCACGGGC | 0.0711525 | 0.174681 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560662 | CTCGGGGAGAAGAAG[-/GGGCACGGGCGGCACGGGC]GGGCACGGGCGGCAC | 10580 |
rs570758637 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379241 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCGTGCCT | 10580 |
rs570760778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467500 | CATGTGAAATATTTC[C/T]GTGAAGGGCCGGCTG | 10580 |
rs570761605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489376 | ATATTGTCTATTTAG[G/T]TATTTGTTTGCTTCC | 10580 |
rs570775209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432956 | AGAGTTTATGAAAGA[G/T]GTTTCAAGCTTCCAG | 10580 |
rs570803172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95497618 | CACCAATGAGCTCAC[A/G]GTTCAACTCTCTGGA | 10580 |
rs570815490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368776 | CCCCACGCCACCCCA[A/G]TTATTCCTCAGAGAG | 10580 |
rs570821921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461060 | AAGTTTTCTTATTGA[C/T]ATTGAGAAAGTATTT | 10580 |
rs570823402 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458276 | TGAAGACAGTCATCT[A/G]TGTGTGCTTGTATGA | 10580 |
rs570832614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95532501 | GCATGATGAGAAGAG[A/G]GCTGGTGGTGCCTCC | 10580 |
rs570838621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427361 | TCTGAACCAACATGG[C/T]CAACGCTCAGACCTG | 10580 |
rs570866662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376679 | TGAAAAATGATATAA[A/G]TAAAGACAGAGGACA | 10580 |
rs570873849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491368 | AGAGATCATCTTTAA[C/T]GGAGATCACAAACTG | 10580 |
rs570875324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419404 | CACCAAAGGGACTGG[C/T]GGGTATGCTGATAAT | 10580 |
rs570883292 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425491 | GACTAAATGAAAGTA[-/TT]TGGCATAAAGCATGT | 10580 |
rs570910421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392376 | TAATTGAATACATCA[C/G]TGATCTATGCCCGGA | 10580 |
rs570933403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454034 | TCATTGTATATCTGA[A/T]TATGAGGTTGATATT | 10580 |
rs570935947 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474710 | GCTCATATAGGATAA[A/T]ATTTATGTTTTAACC | 10580 |
rs570936605 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518663 | CTCTCACCCAAACCG[G/T]AGGTTAGCCGGAAAC | 10580 |
rs570939524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322643 | TCTTATAAATAATAT[C/T]TCTGTGGGTTAACCA | 10580 |
rs570941634 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552164 | CCAGCATTTTGGGAG[A/C/T]CCGTGGCGGGTGGAT | 10580 |
rs570964740 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333290 | GCCTTGCTTTTCTCC[A/C]TCCCATAACGTGTCT | 10580 |
rs570992388 | snp | C/T | 0.00262746 | 0.03615 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356716 | GACAGGGCCTCCTGC[C/T]GCTGGTGCTGTACTC | 10580 |
rs571004130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525187 | GACCTGCCCTGGCAA[A/C]CATTCATGGGAAACA | 10580 |
rs571010121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95559244 | AACCCTAGACTCTGC[A/T]ATCTGTATTGAACTC | 10580 |
rs571031561 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329081 | TTTGTGCTCTGCCAG[A/G]GGAAGATATCAGAAG | 10580 |
rs571040873 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314034 | CTTGAACTCCTACAG[A/G]GAGTAGATCTGGAGC | 10580 |
rs571063305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455119 | TCTGTGGTTAGTCAG[C/T]TAACCTTGCTAAGCC | 10580 |
rs571064536 | in-del | -/TGAAATACGCCT | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437203 | CATCTGTACCAGGCA[-/TGAAATACGCCT]TGGTCCTCGTATCTG | 10580 |
rs571081895 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328315 | AGTTATCTTATTGAG[C/T]TTACTGAGAAAAAGA | 10580 |
rs571097510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446944 | TCAGGAGTTCAAGAC[A/C]AGCCTGGACAACATG | 10580 |
rs571114648 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451895 | GCAGTCTGTTAGAGC[-/T]TGAAAATGGGAAAGC | 10580 |
rs571117564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506635 | CTGGCAATACACTCA[G/T]TACTTAGAAAACAAG | 10580 |
rs571136093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420121 | AGTAGAAAGAAAATT[A/C]TTGGATAGTGACAGA | 10580 |
rs571142775 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532301 | AGGGTGGCCTGCACA[A/C]CCCCTGCACCTCAGG | 10580 |
rs571154520 | snp | C/T | 0.000399281 | 0.0141238 | missense | SORBS1 | GRCh38.p7 | 10:95399118 | TTTTTTCAATAGCCT[C/T]GCCAGGTGAGGTGGG | 10580 |
rs571167853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392855 | GGCCTAAGGCAGTCT[C/T]CCAGTCTGATGGGAG | 10580 |
rs571168949 | snp | A/G | 0.00034664 | 0.0131606 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321941 | GAGAACATGAGAATC[A/G]AAGTTCACCAGGAGT | 10580 |
rs571169708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384443 | CTACACCACGGCAGA[A/G]CACGTTTGAGAGGAG | 10580 |
rs571186030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514299 | GTCCTGCCAGCAACC[C/T]CTGCCACCCACTGAT | 10580 |
rs571201892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412618 | CCAACTCGATATGAA[A/T]ACCTAGGTCTACACA | 10580 |
rs571227060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397795 | CTAACCACAAAGTTG[G/T]AATGGTTGGGCTTTT | 10580 |
rs571227421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441038 | ATAAAAAATAAAATG[A/C]CAGAGTGGGGCCTTC | 10580 |
rs571230544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384867 | AAGAGAAGAATTTGA[A/G]AAAACCCTCATCAAA | 10580 |
rs571255405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483187 | GACCCAAAAACTAAT[G/T]CTTTGTTTCATTAAA | 10580 |
rs571260261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540185 | TCAGAGGAGCTCTAA[C/T]GGCCTCCCATCACTG | 10580 |
rs571288878 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441393 | TTCAGTTTTGTTGCC[C/G]ATATTTGGTGCTGAT | 10580 |
rs571291400 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337535 | ATGTGTGCAGGCAGG[A/G]GGTGGAGGAAGCAGT | 10580 |
rs571291848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533477 | CAATGCCAGGCACAC[A/G]GACAACACTATGCCA | 10580 |
rs571293464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95534093 | GGCCCCCAATCATGC[A/G]GCTTTTTCCTTTTTT | 10580 |
rs571317269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407992 | ATGTTGTCTCCAGTT[C/T]TGAGGTGTGAAATAG | 10580 |
rs571322315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447340 | GGGTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 10580 |
rs571336215 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430609 | CATTTGCTGCCAGAG[C/G/T]ACGGGACAGTTGGTT | 10580 |
rs571367859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548441 | TCATGCATAGTTCTT[C/T]TCTTTCCTTTTTTTT | 10580 |
rs571369653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429522 | AGTCTGCGTTGTATA[C/T]TTAATGAGCACGTGG | 10580 |
rs571376610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429051 | AGCAAGTTGTCAGTC[C/T]GGAGGGTGACATGGA | 10580 |
rs571395134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476083 | AGGTGGCAGTTATTC[A/G]CCCAGGAGCTAAAAG | 10580 |
rs571402938 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540669 | CTCACATACTATTCA[A/T]CCTTCATGGCTCTGT | 10580 |
rs571403207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378553 | GGGGGGCAGGCCCAC[C/T]AAGTTTGCGATGACA | 10580 |
rs571429536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526435 | GCCCCCCTCTCTCAG[G/T]CGCATCCAATGTGCA | 10580 |
rs571448033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344430 | TTTTTTTTAGATGGA[A/G]ACTCACTCTGTCCCC | 10580 |
rs571454504 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560126 | TGGAGTCAGAGGCCT[C/G]ACACGCCAGATAGGT | 10580 |
rs571454594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407228 | CATGCAGAAGCCCAG[C/T]GCAGCTCTGGCCTCA | 10580 |
rs571459858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483970 | TCACACCTGTAATCC[C/T]AGCACCTTGGGAAGC | 10580 |
rs571464104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405719 | GGAGAGAACTTGCCC[A/T]TATCTCCCAACCCCT | 10580 |
rs571472620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377653 | CTTGCCCTCCCTGTA[G/T]TAAATGGATTCTATA | 10580 |
rs571505871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542204 | CCCCACACCGCCCCC[C/G]ACCCTGTCCCCAGGA | 10580 |
rs571516682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462670 | ATCCTGCTGAACTTG[C/T]CTCTGATCCAGGTAA | 10580 |
rs571518478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95470025 | AGGAGATGGGTGGCA[C/T]CTTGCCCTAAAGAGT | 10580 |
rs571535313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436657 | AGGATTCTGGCCCTT[C/G]CTCTTGGTTACCAGA | 10580 |
rs571580771 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384979 | TCCTCTGCAAAGGTA[C/T]TACTCGGAGTGAGTA | 10580 |
rs571591559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457155 | GTTTAGCATTTCCAA[A/C]CTAACAAATGTTAAA | 10580 |
rs571593577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553869 | GATGTCTATATCCTA[A/C]CTGCCATGCCTGGCT | 10580 |
rs571593698 | snp | C/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442569 | ACACGCCTGCTCCCC[C/G]TTCGCCTTCCACCAT | 10580 |
rs571610172 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442587 | CGCCTTCCACCATGA[C/T]GGGAAGCTTCCTGAG | 10580 |
rs571629585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422415 | TCACAGGCACTGACC[G/T]TTGAAAACACAAGGC | 10580 |
rs571639054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95364157 | CATTTGGATAAACTG[A/G]GGGAAAACCAAGCCC | 10580 |
rs571656791 | snp | A/C | | | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414610 | TCTGGCTAATGGGGG[A/C]AAAGGAGCCAGAGGC | 10580 |
rs571662164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455701 | GCACTTTGGGAGATC[A/G]AGGTGGGTGGATCGC | 10580 |
rs571693886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456778 | TACCCTCTCTGCCCA[A/G]GAGAGGAGCTCCCAG | 10580 |
rs571700880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358254 | TGTCAGCTACTTCAA[G/T]TCCACTACCTGGATT | 10580 |
rs571702130 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367765 | TTTATTTTGACTCAT[A/T]TGTTTCAAGCCAAGA | 10580 |
rs571704337 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370252 | ATATTCCTTTTGTAT[-/C]TTTTTTTTTTTTTTT | 10580 |
rs571726611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95330635 | CATGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10580 |
rs571753985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358407 | ATGGGCTCTTAGTAT[C/T]ACAGCCACATTTGCA | 10580 |
rs571781787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463239 | GCTATGGAGATGAAT[A/G]TCATCACTGCCCCTC | 10580 |
rs571784599 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332565 | TCAGCCTACCAAGTA[G/T]CTAGGATTACAGGCA | 10580 |
rs571831373 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95363938 | AATGTTTCTGCCTAC[A/T]CATCATTCCTGTCCA | 10580 |
rs571833084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484807 | GGTGAAATCCTGTCT[A/G]TACAAAAAAATACAA | 10580 |
rs571850172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449906 | GCAAACAAGATAGAC[A/G]GGTTAATATCCTTAA | 10580 |
rs571880505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95400170 | AAGCAATGCAATAAA[C/T]TCTTCATTTACGTTC | 10580 |
rs571890596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352449 | GCCTCATGTGACTTG[C/T]ACCCCTAAAGGAGGG | 10580 |
rs571913121 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95439825 | AGCTAGGCACGGTGG[C/T]GGAGAGGGGCGGATC | 10580 |
rs571936469 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466605 | TCATGTACAGAAGCA[C/G/T]GTGCACACGAAAGAG | 10580 |
rs571944031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393858 | CGTATCTATTCACCC[C/T]CATCTGGATTACTCA | 10580 |
rs571963263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358711 | GCACAGACATGCGCG[C/T]GCGCGCGCGCGCACA | 10580 |
rs571969062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317186 | AATCAGGGAAGGGCT[A/G]GTCTTTGGAAAGAAG | 10580 |
rs571971471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95485554 | TGAGTCATCTCTATG[C/T]TGATAAGGAGACAGC | 10580 |
rs572001805 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482620 | TCTTCTTTCGTGTTT[A/G]TTACTGGCAGCCATG | 10580 |
rs572017124 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358732 | CGCGCGCACACACAC[A/T]CACACACACACACAC | 10580 |
rs572024110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509102 | AAAGGAGCACTTCTT[A/G]GGACTTTATACAAAT | 10580 |
rs572047286 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528390 | CTCTTCGTAACGGGT[C/T]AGAACACAGTGCTGT | 10580 |
rs572052829 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403269 | ATCTGCTACAGAGAG[A/G]GAGGCTGGCAGCCCT | 10580 |
rs572056274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449498 | TCGGCCTCCCAAAGT[A/G]CTGGGATTTACAGGC | 10580 |
rs572068434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95370707 | CTCTCGTATACCCTT[C/T]AATAAACCACATTTT | 10580 |
rs572080792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95324353 | AGAGGTAAAGTGGCT[A/C]AGCTGCTCTTTCCGC | 10580 |
rs572084409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95506963 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10580 |
rs572085389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500563 | TTTTTTTATGCAATT[A/C]CATATGGAAATGATA | 10580 |
rs572088330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530486 | AGAATGAAAGGGAGA[A/G]ACTAATCTAAAATAT | 10580 |
rs572091565 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453075 | CGGATTACTTGAGGT[-/C]AGGTGTTTGAGACCA | 10580 |
rs572097640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323963 | GGTGACAAAGCAAGA[A/C]CCTGTCTCAAAAATA | 10580 |
rs572106483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95380952 | CCCCTTAACCAGGAT[C/T]ACAATTCCAAAACAG | 10580 |
rs572121571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443411 | CAGTGAGCCAAGTTC[A/G]TGTGTGCCACTGCAC | 10580 |
rs572138523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95486861 | ACTGAAGACTATTCT[A/C]CAGCCTCAGCGGTTT | 10580 |
rs572156409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394795 | ATTAAAGCACACAGG[C/T]ATCACACTTAAAAAT | 10580 |
rs572176286 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548219 | CATCAGCTCACATGA[C/G]TAAAGCAGCCCCTGG | 10580 |
rs572177500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386833 | AGCTCCTTTCTTGGA[C/T]GGGCCTGGTGGCTCA | 10580 |
rs572181658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516575 | GATAGATGAAGTAAC[C/T]AGCATAGATTACCCC | 10580 |
rs572185188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549002 | CACTCAAAGATAAGA[A/G]ACCTGTTCCTAGCTC | 10580 |
rs572245614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95542498 | ACCTCTTATCATTCT[C/T]CCAAAATTAGGCTTT | 10580 |
rs572256989 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528845 | AATCGCTTGAACCCG[G/T]GAGGTGGAGGTTGCA | 10580 |
rs572262663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450057 | AGTTAAAAAATATAT[C/T]AAAATAATGACTAAC | 10580 |
rs572274942 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378302 | GAAAAGGGCAGGTAA[C/T]TCACCAGAAAAATGC | 10580 |
rs572282392 | in-del | -/A | 0.493354 | 0.0572595 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552896 | CTCCAAGCGGGCGTA[-/A]AAAAAAAAAAAACAG | 10580 |
rs572309158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541862 | AAGTTTCCCTCCACA[A/G]GGAGGCCTCCCATGA | 10580 |
rs572315884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95479159 | AATGAGTAGATGCCA[A/G]GCAGAGAATATAGCA | 10580 |
rs572317555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516880 | AAAGTTCATTTTCAA[A/G]TTGGAGGGTTGGAAC | 10580 |
rs572320591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352765 | TAATGTTCCTGCCAA[A/G]TCTGATATGTCTCAT | 10580 |
rs572322898 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536458 | TTTTGGTTTTTTGGG[G/T]GTTTTTTTTAATCAG | 10580 |
rs572337709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529284 | GGCTTTTCTTCCTTA[A/C]GGAATATCAAAAACA | 10580 |
rs572346432 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404920 | AGCAGAATGGCTACA[A/G]GAAGCCACAAGGAAA | 10580 |
rs572351431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394182 | CATGAAAAGAGTTAG[C/T]TGCAGGCATGAGAAC | 10580 |
rs572363280 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461765 | CTGCAAAAATGTTCA[-/C]AGTGAATAAAACAAT | 10580 |
rs572365705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424114 | TTCTGATGCAGTAAG[C/T]ATGAGGTGAGGCCCA | 10580 |
rs572368502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424729 | GGTACATACAGGACA[C/T]GTGTTTTGCTCACAT | 10580 |
rs572383226 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442886 | TGAATCTATAGATCA[A/G]TCTGTGGAAAACTAA | 10580 |
rs572385460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535925 | GCAAAAGAATTTAGC[C/T]TTCCAACTTGCTTAG | 10580 |
rs572401712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372727 | GGGACTGTAAGGTTA[C/T]TTTTGTTTTGTCTTT | 10580 |
rs572403524 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522556 | GGTGCAAAATACTGA[A/T]AATGAATGCTTGGCA | 10580 |
rs572448397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410078 | ACAGAGACAAACAGC[C/T]GGCAAGAATGAAGGC | 10580 |
rs572454481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510678 | GTTGTCAAAAGTTTT[C/T]GGAAAGTGAAGGTAT | 10580 |
rs572481097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544420 | TGAGGAGCCCAGGGA[C/T]TCCGAGAAGACACTC | 10580 |
rs572483146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523095 | CCTCATGCTTTTGCA[C/T]TTGAACAGTTTAAAA | 10580 |
rs572483489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346920 | ATTTCTTACGGTCTG[C/T]GACATCATCCAAAAA | 10580 |
rs572484718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537098 | GTCCCTCCTCCTGCC[G/T]CCACCCATCCCCATC | 10580 |
rs572487049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556739 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10580 |
rs572487572 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362396 | AGATTGTACAAGAAA[C/T]CCACCTGCAAATCTG | 10580 |
rs572492016 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323831 | CATCTCTACAAAAAA[A/T]TACAAAAATTAGCTG | 10580 |
rs572529007 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321245 | AACAAAATATGATCA[A/G]TATGTTCCTTACTTC | 10580 |
rs572552305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339496 | GGATGAGGATGCTAA[C/T]GGCAGAGGAGCTATC | 10580 |
rs572560824 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563364 | CACGCCTGTAATCCC[A/G]GCACTCTAGGAGGCC | 10580 |
rs572581752 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451052 | TTCTAGGAGACAAGC[A/T]AAAAATGCCACTGAC | 10580 |
rs572593758 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484547 | AAACTTTTAAAACAC[C/T]GGTGTTTTGTGGCCA | 10580 |
rs572596227 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434967 | CGGTGCCTCCTACCA[C/G]ACCAGGAGCTTGCCA | 10580 |
rs572628165 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493266 | CTGCACTCCAGCCTG[G/T]GCGACAGAGTGAGAC | 10580 |
rs572634058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417126 | GGCTCACACAGCATC[A/C]CTCTCTTCTCAACAC | 10580 |
rs572639931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95472901 | GCCGGGCATTGTGGC[A/G]TGTGCCTATAATCCC | 10580 |
rs572649702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550242 | CCATGCCAAAACAAA[C/T]ATACATACAAAACAC | 10580 |
rs572659448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459190 | TTTATACACTAGATT[A/G]TAAGGGAAAAAAACT | 10580 |
rs572661515 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359634 | GCTCAGGGATGCTCC[A/C]GCTCCGTATACACCA | 10580 |
rs572672229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365722 | CGACTGAGTCACCAA[C/T]CCCACAGTGAATGCA | 10580 |
rs572701334 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327142 | TTCATCTAGTGTTAA[A/G]AATAAAAAAGAATAA | 10580 |
rs572724308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360059 | AAATAAATGTGAGTT[C/G]ATCTAAACTGGCTTA | 10580 |
rs572736332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465127 | GTGTCACATTTAAAG[A/G]GAAGCAAAATTCTTT | 10580 |
rs572741232 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388931 | TTTCCTGTTTCTTTT[A/T]CTTTAATTTATAAAA | 10580 |
rs572766411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95325628 | GCAATCTGGGCTCAC[C/T]GCAACCTCTGTTTCC | 10580 |
rs572771849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495932 | AGTGTTTTTTTGTTT[C/T]TGTTTTTTTTGAAAC | 10580 |
rs572772179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445786 | CAAATTGAGCTTGAC[C/T]GGAACACTGAAAGCT | 10580 |
rs572790344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465465 | CCCGGGAGGCAGAGC[C/T]TGCAGTGAACTGAGA | 10580 |
rs572799024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458335 | TATTTCTAAATTGCT[G/T]TTAAAATTTCATTGT | 10580 |
rs572802863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531035 | GGCAACTACCAGCTC[A/G]CAGCCAGGTAGAGCA | 10580 |
rs572805219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326259 | AAGACATTTCCTTAT[G/T]TAAAAGATACGGTGT | 10580 |
rs572819052 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440485 | GGTGGGGCTGAATCT[C/G]CAGATGGAAACTTCT | 10580 |
rs572829916 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355098 | TAATGATCAATGGTC[G/T]AATTCTGAAGGAAAA | 10580 |
rs572847297 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311649 | CAAGGAGGCGGCAGA[A/G]GGCAGATGGTAAATG | 10580 |
rs572858124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445263 | AACAAACAAGGGATA[A/G]TTTAAAATAAAATTA | 10580 |
rs572865007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95558736 | TAATCAAGGAAAAGG[C/T]AGATGTGAATCCAAC | 10580 |
rs572882333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396065 | ATGCTCTGCCTGTGG[A/G]AGAAGTGGTACCCTT | 10580 |
rs572883540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95453457 | ATTCAGCTACCTCAG[C/T]CTCCCTAGTAGCTGG | 10580 |
rs572885559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461113 | TTCTAAGTCAACTCT[C/G]ATGAGTTGGAGAATT | 10580 |
rs572904853 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489170 | CTTTCTTTTCACTTG[C/T]TATTCCCTCTGCCTG | 10580 |
rs572906841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95452332 | ATACAGGCCCAAAAT[C/T]AATAAGCCCTGAGCA | 10580 |
rs572911160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530349 | TCATCTTGTTTACCT[A/G]TGAGACAACTCCTTG | 10580 |
rs572911601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95316310 | ATATAAAAATTAGCT[A/G]GGCGTGGTGATGCGG | 10580 |
rs572948837 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454265 | CAAAACACACTGATT[A/G]TGTATGCATTCTGTG | 10580 |
rs572966295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95488886 | ACTGGAAGGACCTCC[A/G]ATAGGTTATACAGAT | 10580 |
rs572974997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418784 | TTTAAAAGTTTTATA[A/G]GTTGGGCACTGTGGT | 10580 |
rs572978283 | in-del | -/GAG | 0.00166991 | 0.0288473 | intron-variant, cds-indel | SORBS1 | GRCh38.p7 | 10:95415776 | TCACGTGCAACACGA[-/GAG]GAGTTTTCTGACGCC | 10580 |
rs572989002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95327824 | ACCCTGACCTCCCAG[C/T]GGGACAGTGAGAAAA | 10580 |
rs572990340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354646 | CATGCAGCAGTGCTG[A/G]CTGGACTTGGCATTT | 10580 |
rs573011594 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320189 | TGCCCCACGCTCAGC[C/T]AAGAGCTCTCACTCT | 10580 |
rs573054168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350587 | AACTCTCTTACCCTC[C/T]GTGGGTTTTTCCTAA | 10580 |
rs573059564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466270 | CATGGTGAAACCCCG[G/T]CTCTACTAAAAATAC | 10580 |
rs573063222 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428488 | TATGGTCATCTCCAA[C/T]TTACAAATAAGGCAA | 10580 |
rs573072336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383043 | GGTAGAGGTGTGAAA[C/T]TGGATGTGTATTTAA | 10580 |
rs573099514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474185 | AGAGAGTTCAATGTT[C/T]GTGCATGGGTATATG | 10580 |
rs573103007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480902 | CAGAAACAGTTGCCC[A/G]GGAGTGATTCCTGGG | 10580 |
rs573105096 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351517 | CAGAACGGCTGTAGA[A/G]CCACAACTATTACAC | 10580 |
rs573118890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551432 | GGAAAAAGATCTACC[A/G]GCGCTGATATCTAGG | 10580 |
rs573119459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524896 | CTAATGACTTGATGA[C/G]AAGCTAGAGAAGGGT | 10580 |
rs573147004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95518255 | GAATAAGTAGCAGAG[A/C]CAGAACTATTAATAG | 10580 |
rs573177002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361643 | TGTAGTTTTAGTAGA[A/G]ACAGGGTTTCATTAT | 10580 |
rs573202909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446541 | CTGCAAAGGTTCTTG[G/T]AAAACAAACAGCCTT | 10580 |
rs573204893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362508 | CATCTTAAACTCAAC[A/G]TGTCCCAAACCATCT | 10580 |
rs573214919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356385 | GAGGTCAGGCTGCCC[C/T]GGGACAGCACAGGTG | 10580 |
rs573223204 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419711 | GAAGAAAGGGGATAG[A/G]CACAGTGACTTTACA | 10580 |
rs573238024 | snp | A/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442244 | ATGGCTGGGTCAATT[A/T]CTGGACTCTTTTCTG | 10580 |
rs573260431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545520 | AAACCCTGCCTCTAT[C/T]AAAAACAAAAAAAGT | 10580 |
rs573270979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419490 | CTTTCAGCTCAAATG[C/T]CCCATATGTGATTTC | 10580 |
rs573278789 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377933 | CCTGAAGTAATTAAC[G/T]TATTTTATTCCCAAA | 10580 |
rs573287501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552216 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCCA | 10580 |
rs573297427 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347805 | AGGGCAGTGGCACAA[C/T]CATGGCTCACTGCAG | 10580 |
rs573306516 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505004 | AGAGGAGCAGCTGCC[C/G]TCGTGTACAGGATAC | 10580 |
rs573311839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367981 | CCTCTGGGTGGGTCA[A/G]GAGAAGGCCTCCTGG | 10580 |
rs573329409 | in-del | -/TTATTT | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444083 | TAAGGTTTTTATTCC[-/TTATTT]TTATTTTTATTTTTG | 10580 |
rs573356529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440531 | GTTGGAAAGCTGACA[C/G]CTCTTAGCTGCATGA | 10580 |
rs573360807 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559449 | AGGCCAACAAGGCGG[C/G]TATCGTCCACAAGAT | 10580 |
rs573386314 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463858 | GGCAGTGACAGGTAA[C/T]CAAGGTGAGAGAACC | 10580 |
rs573417372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95412245 | TGGATCATATGAGCA[C/T]TAAGCACTTTACAGA | 10580 |
rs573422141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343389 | CCTCCCGGGTTCAGG[C/T]GATTTTCCTGCCTCA | 10580 |
rs573426446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546294 | CAGTCCTTTCTTGCA[C/T]TGCTATAAAGAAATA | 10580 |
rs573426832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397385 | AGTAACAATATCTGA[A/T]TTCAAAACTCAGCCA | 10580 |
rs573443107 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95369440 | GTTCCAACTGCCTAC[C/G]GGATATTACCTATAT | 10580 |
rs573455367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491399 | AAAGCACAAGGGGTG[A/G]CATCCAACCTGTGGA | 10580 |
rs573456119 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557895 | GCCTCCTACTTTCTC[A/G]TCTGTTTCTCCAATC | 10580 |
rs573465838 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415005 | AGTACATGAGACAGT[C/T]GGAGCTGGCCAGCTG | 10580 |
rs573481785 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530806 | TCTCTGCCCACCCTG[C/T]ACATGTTACCTGCCC | 10580 |
rs573485175 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344862 | AAACACTGAGTTAGG[-/A]GGAAGGAGCCCTCTC | 10580 |
rs573504325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407350 | TACTAAGGGGACCTA[C/T]GGTTCCCACACACTA | 10580 |
rs573511296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514482 | CTTTGCATCTAAGAG[A/C]TACTGTGGAGATCAA | 10580 |
rs573512089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397876 | TTTTCACTCCCACTT[G/T]ACAGAAGAGGAAATG | 10580 |
rs573516493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418614 | GGCCAGACTGGTCTC[A/G]AACTCCTGACCTCAG | 10580 |
rs573516944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538666 | ATGTAACCCTTCCTC[A/G]GAGGTTTCTGATGCT | 10580 |
rs573549466 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345973 | TGTTGTAGCAAAATG[A/G]GTAAAGTTATCTCCC | 10580 |
rs573554723 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394353 | GCTTTGACCAGAGCC[C/T]CACATGTTCAAAACA | 10580 |
rs573566235 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488366 | CTCATTTGTATAATT[C/G]ATATTTGCATAAAAT | 10580 |
rs573576134 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490571 | GGGCTGACTATGGCA[G/T]CTACACTGTAACACT | 10580 |
rs573587575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95475081 | ATGCAGTTAGAATCT[A/G]TAAGAGGTTTAAACT | 10580 |
rs573594541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533000 | ACAACCTTGATATTA[C/T]CATGCTTCAAATGTC | 10580 |
rs573604615 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421085 | GGTGGGAGAATGGCT[A/T]GAGGCCAGCCGTTGG | 10580 |
rs573626704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520457 | CTAACATGGTGAAAC[C/T]CCATCCCTACTAAAA | 10580 |
rs573630816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343960 | TTTTTGCCACAGCCC[C/T]CTTTGGGGGGCATTA | 10580 |
rs573640099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95428464 | CTCATTTAATCTCAA[C/T]AACTCTGTTATGGTC | 10580 |
rs573647885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328671 | AAATTCCAGATTTTC[C/T]AAATTCTCGATTTGT | 10580 |
rs573651045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367195 | ACTATAGATGCATAG[C/T]ACCATACCCAGCTTT | 10580 |
rs573684954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329314 | CCTCCCAGACCCAAG[A/C]GCTCTTCCCATCTCA | 10580 |
rs573686476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95468665 | CCTAAGGTGCTATTT[C/T]CTCTTGTCTACTGAT | 10580 |
rs573701296 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462449 | TCACCACCCTAACAC[A/T]ATCTCATTATTTGCT | 10580 |
rs573721464 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95338400 | TGGATCTGGTCTATA[A/T]GGCTGATGAGAAGGT | 10580 |
rs573739398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437223 | TACGCCTTGGTCCTC[A/G]TATCTGATCTGTCAT | 10580 |
rs573763777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399724 | GCAAGCTCACAGCAA[C/T]GTGGTGAGAGGACTT | 10580 |
rs573766333 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378924 | AAGTATCCTACTATG[A/G]TAAGAGGGGACCAAG | 10580 |
rs573773420 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344760 | GTAAAACCAAGTGAC[C/T]GAAGGGCTTAAAAGA | 10580 |
rs573774107 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510329 | TGGGGGAGAAAAAGC[-/T]TTTTTTTTTTTTGAG | 10580 |
rs573779717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95427758 | GCCAAGAAACTTGAC[A/G]TGTCAAAAGATGGAA | 10580 |
rs573779766 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434216 | AGCTGCTTCAAATTC[A/G]GCTAAGTTCAGAGGT | 10580 |
rs573801129 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385293 | AAAAAGAGTTAGTCT[A/G]AAATAGTTAGCCTTT | 10580 |
rs573811982 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342671 | AACTCCTGGGCTCAA[A/G]TGATCCTCCTGCCTC | 10580 |
rs573843249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357216 | AGGGCTTTTAAAAAA[A/T]TTCCAGTCGAGGTCC | 10580 |
rs573858917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430137 | AAAAGTATTCTGGGA[C/T]AAGAGAGTGTTTCCA | 10580 |
rs573859326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331137 | TGAATCTTTTGTTTA[C/T]GGACAGAGTAGCTGC | 10580 |
rs573864535 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414002 | AAAAAAAAAAAAAAT[C/G]CTAGTCTCTGTCATT | 10580 |
rs573871338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95561278 | CCGGCGCTGCCGCCG[C/G]CGAGCGGGCAAGCGC | 10580 |
rs573883126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547611 | GGTGGCGGGCACCTA[C/T]AAGCCCAACTACTCA | 10580 |
rs573887737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528683 | CAGCACTTTGGGAGG[A/C]CGAGGTGAGTGGATC | 10580 |
rs573909969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95493205 | TGAGGCAGGACAATC[A/G]CTTGAACCAGGGAAG | 10580 |
rs573923682 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511993 | CAGGATTTTTTTGTA[A/T]CCTAGATGCTAGACA | 10580 |
rs573929489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344880 | AAGGAGCCCTCTCTC[C/T]GGCATTAGCAATGTT | 10580 |
rs573938623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461969 | CTTTAAGACTATTTC[A/T]TATCATAATCCATAA | 10580 |
rs573944522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394005 | CACAAATGTGACTGT[C/G]TTCCCCAGCAGGTAC | 10580 |
rs573976203 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350525 | GCTTTCATAATCTAG[G/T]CTTGGAAATGTCAAA | 10580 |
rs573991507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429779 | GCCCGAAAGGAAGAT[A/G]GCTGACTACAAGTCC | 10580 |
rs573992417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548021 | ATGGTAAATGTCCCA[A/C]CCATTCCATGATGGA | 10580 |
rs573998881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95492715 | ACAGTGAGAAATGGA[C/T]GACAATGGAGGCAAA | 10580 |
rs574015368 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393584 | GGGCCCACTGTGTGC[C/T]GGCAAGGTTTTCTGT | 10580 |
rs574033672 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493191 | GCTACTCAGGAGGCT[A/G]AGGCAGGACAATCGC | 10580 |
rs574038702 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548798 | GGTCATCTAATCCTC[C/T]CTGCAATCCTGTGAG | 10580 |
rs574040585 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95484330 | CAAAAGCCTGAGAGG[A/T]TCAAACAGGTAGCAA | 10580 |
rs574054355 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95317837 | AGACCAGCCTGACCA[A/G]CAAGGTGAAACCCCA | 10580 |
rs574064779 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537491 | TAAACCTATCACACG[C/T]CCCTGGGTAGAGCGG | 10580 |
rs574073680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95450284 | GACAATAATGCTATA[C/G]ATACAGAGATGTTTA | 10580 |
rs574079965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95556087 | TCCATGGAAGGAAGT[A/C]TAGAAACAGGGTACA | 10580 |
rs574101564 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539252 | CCTCAGCACTGCTGA[C/T]ATTCTGCATGGGGTA | 10580 |
rs574117617 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344960 | TGACAGGGTTGCTCT[-/A]AAAAAAAAATTGTTT | 10580 |
rs574169673 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464048 | GAATGTAGGCTCAGG[C/T]AGGGGCAGTGGATCA | 10580 |
rs574172030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521432 | TCTCTCTTAGCATTT[A/T]TTTTTTAATGGAGTC | 10580 |
rs574178073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331968 | TTGCTGACGTTAAGG[C/T]ACCAAAACATCTACA | 10580 |
rs574195082 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351866 | CCTATTAAACCTGCT[A/G]TAGGCTTCTGCTAGT | 10580 |
rs574207862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386427 | TATCGCTTGAGGTCA[A/G]GAGTTTGAGACCAGC | 10580 |
rs574211999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457437 | AACGGGAATAAAAGC[A/G]GCACTAACCTCCCTG | 10580 |
rs574223491 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415153 | GTGTTTAACCCCACA[A/C]CACCACCATAGAGCC | 10580 |
rs574229442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95338810 | GCCTCCCAGGTTTAA[C/G]CGATTCTCCTGCCTC | 10580 |
rs574254637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477791 | CTTCCCTGGGCCATA[C/T]TGGAAGAAGAAGAAT | 10580 |
rs574285211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522205 | TCCCAAGGCCCAACC[A/G]AAAGGTGCCTCCTTT | 10580 |
rs574295858 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558542 | GTAACCATGAATAAA[C/T]CAGCAAGTTAAACAT | 10580 |
rs574317677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477041 | GCACACTCCCAACAC[C/T]GAGCTGCAGAAAAGT | 10580 |
rs574357037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95549086 | AATCATAAATGTCGG[G/T]TCTAGAAACACAGAA | 10580 |
rs574393376 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95420003 | CTAAGAGGTAATGCA[C/T]GACCTAAAGGTTCCT | 10580 |
rs574398559 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543718 | GGGTGTTTCATTCTC[A/G]TTGTATTCCCAGGAT | 10580 |
rs574404937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464586 | TAGCCCACTCTTTGT[A/C]CCACACATGTGACAG | 10580 |
rs574408842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543209 | CCCAACCCACATGCC[A/C]TCATGGCACCCTGTA | 10580 |
rs574415397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443715 | TTCCTTTCTGGATGG[C/T]TGCTTTGCCTTACTG | 10580 |
rs574460663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95494392 | GCGCAGGACTCTACC[A/G]GTCAATGCAGCGCCT | 10580 |
rs574468307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95374425 | AAACAGACTTGAAAA[A/G]TCAACGGCATGGACT | 10580 |
rs574491443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95509181 | ATATGAACAGAAGCC[A/G]TCTTTTGAGAGTTTC | 10580 |
rs574512601 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437565 | CACATTCTGCAAGAA[A/G]GAAAGAGAGCATGAG | 10580 |
rs574525561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480092 | CAACACATGCTAAAT[A/C]GGGGCAATGTGGAGA | 10580 |
rs574525655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95471973 | CAGCTAACAAACCCC[A/G]ATGTGGCAATTTTAG | 10580 |
rs574535027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95387852 | CCTGAAGCCTTTGCC[C/T]GATTTTTGCATCCCC | 10580 |
rs574537234 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494867 | TATTTTTATTTATTT[A/G]TTTATTTATTTATTT | 10580 |
rs574562673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95510724 | CTCACACCTATAGTC[C/T]CAGCTACTGGGGAGG | 10580 |
rs574566291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502219 | TTTCTGTCAGTAAAA[C/T]GTGGCCTAGAAACTC | 10580 |
rs574571737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495061 | CAGCCAATTTTTTAT[A/G]TTTTTGGTAGAGACG | 10580 |
rs574610155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95438152 | ATAGATAAGAAAACT[A/G]AGGCAGAGAGGATTC | 10580 |
rs574630246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95501378 | GGTCACAGGCCTTTT[C/T]CCAGCAAATGGCTGC | 10580 |
rs574654416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95483996 | GAAGCTGAGGTGGGC[A/G]GATAGCTTGAGGTTG | 10580 |
rs574670280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487687 | ACTAAGGCGCCCAAC[A/G]AGGAGATGGAAGAAG | 10580 |
rs574672633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521916 | CCCTTGCCTCGGCCT[C/T]CCGAAGTGCTAGGAT | 10580 |
rs574688366 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526617 | TGCACAAGTTTCCAG[A/G]TGATACTGATGCTGG | 10580 |
rs574701319 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95503287 | TCACCACTCAGATCA[G/T]CTGGGCCCAGCTTCA | 10580 |
rs574712372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431013 | GTGCCCTGGCACCTG[C/T]TATGGGTAGCTGGGA | 10580 |
rs574719410 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470565 | ACAACCTAAACCAAG[C/G]ACCACTAAATCTGCA | 10580 |
rs574730317 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474972 | GCAAATGACATGGCT[C/G]CCCTAAGGGGTTCTG | 10580 |
rs574740149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530215 | CCTGCTGCATTTCCC[G/T]TCATCCCAGCTCCAG | 10580 |
rs574765126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417897 | TGCTGGGATTACAGG[C/T]GTGAATGGCTCCTAT | 10580 |
rs574800957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536938 | ATCCCTCTAACGGCT[C/T]GAATTCAAGATTCTC | 10580 |
rs574818085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95529432 | GTCCAGTTCCTGTAG[A/G]CATACAGCTGAGGAG | 10580 |
rs574832163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95388691 | CTATGCCAGTGATTT[C/G]CAGGAAGCTGTAACA | 10580 |
rs574834892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95332859 | GAACACAGGGAAGCA[A/G]AGGGGGCTGAGAGAG | 10580 |
rs574839806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504154 | GAGTTCATTCTCCCT[G/T]GTCTGCAGATGAGCG | 10580 |
rs574846277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95517582 | TCACAAAGCCCATGA[A/T]GTCAGGGCTCAGGTC | 10580 |
rs574846932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425212 | ACTTCGTACATGCAA[C/T]TGGGGACACATTATT | 10580 |
rs574867717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516919 | CATTTTCCCATGGAC[A/G]TGACATGGAGATAGT | 10580 |
rs574868250 | snp | C/G | 1.65053e-05 | 0.0028727 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384002 | TTCTGAGCTTGACTT[C/G]AGTGAGGAAGAGCGG | 10580 |
rs574888570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531158 | CTCTGCCCACCAAAC[C/T]GCGAGCCAGAGCCCC | 10580 |
rs574888770 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469701 | GTTCATAAAATACCC[A/C]TAGAAGGGGAGAGAA | 10580 |
rs574941651 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SORBS1 | GRCh38.p7 | 10:95360819 | TCAGCTTTGGCCAGA[A/C]CTTTTTTTTTTTGAG | 10580 |
rs574954358 | in-del | -/AAAAC | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543401 | GAAACTCTGTCTCAA[-/AAAAC]AAAACAAAACAAAAC | 10580 |
rs574960555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95396563 | CTGGAGTGCAATGGC[A/G]CAATCTTGGCTCACC | 10580 |
rs574992482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537927 | AGTTCGAGACCAGCC[C/T]TGGCAACATGGCGAA | 10580 |
rs574995180 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312574 | GACAAAAGAGCAATT[G/T]GAAATCTCTGTTTCT | 10580 |
rs575008370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410917 | AGATACATCGTATCA[G/T]TAATTCCAGTTAGAA | 10580 |
rs575021526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397125 | GGTCCAACTGCAGGA[C/T]CCAGTCTTCTGGCAT | 10580 |
rs575025178 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355122 | AGGAAAAAAAAATTC[A/C]ACCCCCCACCCCATT | 10580 |
rs575027654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531811 | ACATGCACAGGGGCC[A/G]ACATGTGCATTGTGT | 10580 |
rs575035333 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545034 | ATAGAGGCCCTGCAA[A/G]GCAAACACAAAATAG | 10580 |
rs575046393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95419741 | ATGCAGGGAACTACT[C/T]TTTGTTGTAAACATT | 10580 |
rs575051153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544665 | CAAGGGCATCTTACA[A/G]CGTCCTCATGACATC | 10580 |
rs575063920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95418509 | TCCTGCCTCAGCCTA[C/T]TGAGTAGCTAGGATT | 10580 |
rs575072700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550759 | GAACACCCATGTTTA[A/T]CTCTGCTCTCTTCTG | 10580 |
rs575093609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459840 | AAGGGAGATTTCAGG[A/C]AACTGCCAGGAAGAT | 10580 |
rs575097029 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432316 | GGACCGTAAGAGACA[C/T]ACACACACACACACA | 10580 |
rs575102970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525395 | TTCTTTTAATGTATT[A/G]TTTTTAATAGATTCC | 10580 |
rs575110935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95420417 | GAATTAATCAGCACT[A/G]TTTCTTGATCTGCAT | 10580 |
rs575116753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321374 | CTTCATCTCTATCTC[C/T]TCCATGAACCATATG | 10580 |
rs575129339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445904 | TAAAAACCTCTAACA[C/G]TTAATATTTATTTAA | 10580 |
rs575137646 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511402 | TATTTTTGCAGAGAT[-/G]GGGGGTCATACTATG | 10580 |
rs575138432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489567 | AGGGAGGCATAGGCA[C/G]AGTCTATCTTACGAC | 10580 |
rs575142110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95334642 | ACCCCTAACCTTACT[C/T]GGAGATCCGGCACCG | 10580 |
rs575148879 | in-del | -/AAAC | 0.228547 | 0.249078 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477863 | TGATGAGCTAAAACA[-/AAAC]AAACAACACACACAC | 10580 |
rs575156325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95489042 | GGCCTACAGGGTCTG[C/G]CTCTCACCTACTGCT | 10580 |
rs575171410 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440813 | TGTAACACATATGTC[A/G]AATTTTATCAAATTG | 10580 |
rs575173418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538469 | ACTGCCCTCAGGAGA[C/T]GGGCTGCTCTGACTG | 10580 |
rs575178338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426893 | GGAGGGTGCACTCTT[G/T]TGAGGACTTTTCCCT | 10580 |
rs575202401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320128 | CTCATACTCCTCAGA[A/C]CATTGTCCCATGGGG | 10580 |
rs575214721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447073 | TTGAACTCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10580 |
rs575221018 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552894 | AGTCTCCAAGCGGGC[A/G]TAAAAAAAAAAAAAC | 10580 |
rs575229444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451731 | TCTTCTGAAGCAGTC[A/G]CTATACAATGTCTAC | 10580 |
rs575239789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320524 | AGCTGGGACTACAGG[C/T]GCATGCCACCACGCC | 10580 |
rs575247897 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95508545 | GGTTGGACAAACTGT[-/CA]ACCGTCAAGAATGCT | 10580 |
rs575269963 | snp | C/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95390009 | AAGGCCAGTAGAGAA[C/T]TATTTTAACTCAACT | 10580 |
rs575279074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552335 | TGAACCCGGGAGGCG[G/T]AGGTTGCAGTGAGCC | 10580 |
rs575283086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350650 | GTGAGGCGCACTACT[A/G]CAGCACTGCTGAACA | 10580 |
rs575301190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447013 | GGGCATGGTGGTGGA[C/G]GCCTGTAGTTCCAGC | 10580 |
rs575321553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95342684 | AAGTGATCCTCCTGC[C/G]TCAGTCTCCCAAAAT | 10580 |
rs575336854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460586 | GCGTGGTGGTGTGTG[C/T]CTGTAGTCCTACCTA | 10580 |
rs575353545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95546883 | CTGGGACTACAGGCG[C/T]GTGCCACCACACCTG | 10580 |
rs575386556 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545489 | GGAGTTCGAGACCAG[C/T]CTGGTCAACATGGTG | 10580 |
rs575389202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95361805 | TCTTCTAATGTTGAA[A/G]AGAGACCATTTGTTT | 10580 |
rs575408755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344104 | GCAGCTGTGGAGGGG[A/G]ATGGGAGCATAATGG | 10580 |
rs575458533 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316995 | TTTCTACTGAACAGA[C/T]GACTCAAAGTAGTGA | 10580 |
rs575490106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95368078 | CATGGACAGCACATC[C/T]TCCACCAGCTTCTCC | 10580 |
rs575491809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512200 | AAGCAGGCAGATTAC[C/T]TGAGATCAGGAGTTC | 10580 |
rs575518138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351112 | GACAGATGCTGTTTG[A/G]AGAACTAAACTGGCC | 10580 |
rs575518185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343448 | TGCGCCACCAGGCCC[A/G]GCTAATTTTGTATTT | 10580 |
rs575528997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95455191 | AATCTCATAGCATTA[C/T]GGTGAAGATTAAATA | 10580 |
rs575536506 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388705 | TGCAGGAAGCTGTAA[C/T]ACTGCATGGGATTTA | 10580 |
rs575544814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95474298 | TGGGTATGTCACCTC[C/T]ATGCCACCAAAGAAA | 10580 |
rs575549543 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406635 | TCTAGTAGTTGGGTA[C/T]GATTATTCTTTCCCA | 10580 |
rs575554498 | snp | A/C | 0.000121367 | 0.007789 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356426 | GCTCAGCCTTCCGGA[A/C]AGGTCCAGGGATGGC | 10580 |
rs575605287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95469520 | GTTTGCAACATCCAC[A/G]GAGACTCTCAGAGAC | 10580 |
rs575626801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376391 | CTGCAATAATTTTCA[G/T]TAATGTGGAAGAAAA | 10580 |
rs575646591 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461164 | TTTAAAATTATTCTC[A/C]CATGTGCCCTTCAAC | 10580 |
rs575668715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95476266 | AATTAGACTACTCAA[C/T]TTCCAGGGCAAAAAC | 10580 |
rs575675542 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408589 | AAAAAGGGGGGGGGG[A/G]GCAGGGAGGGAGGCA | 10580 |
rs575697177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95362531 | AACCATCTTCCATCA[C/T]ACAACCCAGAAAGCT | 10580 |
rs575712209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355030 | AACCAGCTTGCGAAA[A/C]GAGTTCACCTTTCAT | 10580 |
rs575718386 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505818 | ACAACAGTTCCCATG[G/T]CAGCCCTGGCTCCTG | 10580 |
rs575732584 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472622 | TCTATAAGCTTAGAT[A/C]GACTAGTGATTTTAA | 10580 |
rs575734451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95389029 | AGGATGGGCAAAAAT[C/T]ATTTGCATAACCACT | 10580 |
rs575757163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434331 | GATGTCCATGCACCG[C/T]AGACCCATCCCAAAG | 10580 |
rs575763919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95343380 | CAACCTCCGCCTCCC[A/G]GGTTCAGGCGATTTT | 10580 |
rs575770509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446500 | AGGAAGAAATTGAGC[A/T]TGTCTGTAAAAATGA | 10580 |
rs575783662 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384659 | AGATGGATCCCCGGC[G/T]GCACCAGCTCAGTGT | 10580 |
rs575796576 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314901 | TACACAGTAACCTTA[C/G]ACAGGCTTGGGTTTT | 10580 |
rs575816826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95491490 | CTATCACACAAAAAC[C/T]CAGATTTCTGGCTTC | 10580 |
rs575848095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499719 | TGAGTGCGGAGAACA[C/T]TCCTAACAGTTTGGT | 10580 |
rs575922795 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375472 | GTCACCTATAATGGG[A/G]TTGCATTTGTGGGTC | 10580 |
rs575933184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337506 | GCGTTTGAGCATGTG[A/C]GAGCGTGATCCTGAT | 10580 |
rs575960992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560369 | TAATAGCGTAATAAA[C/T]TCTTGTCTGCCTGGA | 10580 |
rs575979360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526928 | CAATCTTCTTTCCAC[C/T]GTACTAACACCAGGC | 10580 |
rs575979853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95462821 | TATTTATTGCTAGGG[A/G]AAAAAAACCCTATTG | 10580 |
rs576025765 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95372660 | TGATAGTGGTAGAAA[C/G]ATACTTTTCATCCCC | 10580 |
rs576025985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95528078 | AGCCACTTTCTGGGC[A/C]CCCACTGTGGGCAGA | 10580 |
rs576036726 | in-del | -/CTC | 0.0023933 | 0.0345097 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430866 | AGGACCAAGAAGCTA[-/CTC]TGTTGACTTTTAGGG | 10580 |
rs576037000 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327274 | CACACATACACACAC[A/T]CACACACACTGCACT | 10580 |
rs576040164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95526061 | TCCTTCACCAACCCT[A/G]TGCCTGACACATGCT | 10580 |
rs576055416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337670 | TCCCAGCCAACCCAG[C/G]CCCTGTGCATCCAGA | 10580 |
rs576058346 | snp | C/G | 0.000399281 | 0.0141238 | missense | SORBS1 | GRCh38.p7 | 10:95421970 | GCCTACCTGGGACTT[C/G]TCAGAAGGAAGGTTG | 10580 |
rs576063424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560980 | AGCAGAGGCCATGAT[A/C]GTACTACCCCACACC | 10580 |
rs576064990 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433853 | ACTTATCCAACTCTA[A/T]CAAGAGGCTAAGCGA | 10580 |
rs576073586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378727 | AATATCTGTCCGTCC[C/T]ACTACATATATGTGT | 10580 |
rs576094227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95522263 | TTATTCCCCTTTTGT[C/T]CTTCTATTCAACCCA | 10580 |
rs576118696 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554162 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCAG | 10580 |
rs576122558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358375 | AGTGACCAAGTGAAA[C/T]TGGAACCTGGGATTC | 10580 |
rs576127957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95323915 | GAGATTCAGGCCACA[G/T]TGAGCATGATTGCAC | 10580 |
rs576129682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95514536 | ATGGTTTTGATATCT[A/G]TCAAACCAGGTATCA | 10580 |
rs576145628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352142 | AAATATTAAAAAAAA[A/C]CCCTAAGAATAACGC | 10580 |
rs576164302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394745 | GACAAATCCCAATTG[A/T]CTCTTTCGAATGACT | 10580 |
rs576180765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95424657 | CAGATTTTGGTATCC[A/G]TGAAGGTCCTGGAAC | 10580 |
rs576182409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95416181 | GGGCGTGGGGGAGAG[A/G]GAACCTTTAGCAATA | 10580 |
rs576189929 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426537 | GTGGGCAGTGGATCA[G/T]GCCTATGTAATGGAG | 10580 |
rs576195099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421217 | GGAGAGAGAGGGGGA[A/G]AGAGAGAGAGAAGTA | 10580 |
rs576210050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95463734 | TTCCAGTAAACACAA[C/G]GCTCTTTTTAGCACT | 10580 |
rs576213097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95553990 | CCTCCCAAACTGCTA[C/T]GATTACAGGAATGAG | 10580 |
rs576214902 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408664 | TATTCCCTCAGGAGA[C/T]TTTGCAATAATTAAG | 10580 |
rs576247011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95535307 | TTTACTACTGAACTG[C/G]GTTTTCCTAAGTGAA | 10580 |
rs576249893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318021 | GAGTGAGATTCTGTC[C/T]CAATAAATAAATAAA | 10580 |
rs576273211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95456680 | TGACTGCCTGTGAGC[A/G]GGTTGGGCCACAAGA | 10580 |
rs576273349 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407427 | CTTAAAAGATCATGT[G/T]GCCAACATGGCGAAA | 10580 |
rs576280265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95449480 | TCAAGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 10580 |
rs576291048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95548076 | CATGGGGACAGGGGA[A/T]AGGGGTGTGGGGACC | 10580 |
rs576293982 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403113 | CCTCTCTACACCCTA[C/G/T]GCCAGCCTCTCTCTC | 10580 |
rs576310135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95541735 | CCCCTCCCCTCTTGC[A/G]GGGATTATCTCCTCT | 10580 |
rs576349181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477192 | CTCTCTGCCAGCCCA[A/C]CCCTAGCCTGTTCCT | 10580 |
rs576353306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95429887 | TCATCACAATTCCAA[C/G]TGACTCATGCAGCAC | 10580 |
rs576354585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95547677 | AGTGAGCCGAGATCG[C/T]GCCATTGCATGCCAG | 10580 |
rs576381377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95415105 | CCTTTTAACACTTTA[C/T]GAGAGAGAAAGAACA | 10580 |
rs576381902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95379715 | CTGTCACTAGTTAGT[A/G]TACTTACCCACAGTT | 10580 |
rs576384622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95430230 | TTGCCAGGCCGAGGC[A/G]GGTGGATCACTTGAG | 10580 |
rs576391931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95331286 | GAAGACCCCTGCATT[C/T]ATTTCATTCACTCTC | 10580 |
rs576406605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95444557 | CTGGACAGCTTTGTG[C/T]TCTAATTTTTAAATC | 10580 |
rs576412743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550211 | TATAAACCAAACACA[A/G]TCAACTCAGTGTGGC | 10580 |
rs576416506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543300 | GCTACTCAGGAGGCT[A/G]AGCCAGGAGAATCAC | 10580 |
rs576417654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448788 | TGACAGAGAGAATAA[C/G]GAATGAATAAATACC | 10580 |
rs576442798 | in-del | -/A | 0.39979 | 0.200158 | intron-variant | SORBS1 | GRCh38.p7 | 10:95552402 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10580 |
rs576450896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95317063 | AGTTCTCTAAGAGGC[C/T]GGTGAGGACAAGGCA | 10580 |
rs576454707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95407655 | ATGAAAAAGACCACG[C/T]TGGCCAGGCACGGTG | 10580 |
rs576468338 | snp | C/T | | | missense | SORBS1 | GRCh38.p7 | 10:95410738 | GGGAATCAGTTCCAA[C/T]AAGGGAAGAAGAAAC | 10580 |
rs576469111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95445195 | GACTTTTTGAGTAGC[A/G]GGTTCTGTTGTGTGT | 10580 |
rs576471422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437719 | ATGAGGCCCTCTGCC[A/G]AGAATGCCTCCTCCT | 10580 |
rs576471488 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399509 | AAGCCTTGCCAACAG[C/T]GTGATCAGAGCTTTG | 10580 |
rs576475954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346181 | GTCTCTTGGTCTCTT[C/T]ATTTGAACAGTGGGG | 10580 |
rs576487140 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95436147 | CCAAGGAGAGAGTGG[G/T]ACTCACTCCACCTGC | 10580 |
rs576514714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377877 | AAATAAAATGTACCA[C/G]CTCTTTCGGGGAACT | 10580 |
rs576515832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386496 | CAAAAATTAGCCAGG[A/C]GTGGTGGCATGTACC | 10580 |
rs576516394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339420 | TGTCCTGCATTGTTT[A/G]TCACATCCTTAGCTC | 10580 |
rs576545559 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479286 | GCTCCCATGTGGCTA[G/T]AAGCGAAGAAGGTCC | 10580 |
rs576554870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95543966 | CTCAAACAGGAGAGT[A/G]TCACCTAGGAAGCAG | 10580 |
rs576567013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95457467 | GTTGTGAGGATTAAT[C/T]GAGATAACCATTTAC | 10580 |
rs576589783 | in-del | -/GGA | 5.08638e-05 | 0.00504275 | cds-indel | SORBS1 | GRCh38.p7 | 10:95339163 | GGCACTGCGACTTGG[-/GGA]GGAGGAGAAAGGCAG | 10580 |
rs576599332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95409391 | CTCCTGCATGGTTCC[A/G]TGTGGGAGCTGGGGC | 10580 |
rs576609584 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562480 | TGCTGGCCCAAGGTC[A/G]CAGAGCCAGCAAGTA | 10580 |
rs576612166 | snp | G/T | 0 | 0 | intron-variant | SORBS1 | GRCh38.p7 | 10:95443360 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATTGCTTG | 10580 |
rs576620962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358928 | ACATCAACTAACATA[C/T]AGAACAGCTTAAAGA | 10580 |
rs576681647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372604 | CTAGACAATTTCATA[C/T]CAGTAGTTTTAAAAC | 10580 |
rs576690553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95365135 | TCCTGACTGCCTGTG[A/G]TAGCATTTGCCACTT | 10580 |
rs576695503 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423264 | TCTCAGATGCAACTA[C/T]TTGGCTCTGCTATTG | 10580 |
rs576698734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95465077 | AGCTAGCTTTGCCTT[C/T]CTACAGACCAAATGG | 10580 |
rs576704479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95516478 | CTTCTAATCCTAAGG[C/T]TCTGTAGTTCATTTG | 10580 |
rs576710179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95340329 | ATAAGTTGTTTCACC[A/G]AAGCCTCTTACAACC | 10580 |
rs576722497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354197 | GGCTGATATGAAGAA[C/T]TTCCTCTTCCCAAAT | 10580 |
rs576750467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95451581 | TTGGAGCCTTCTCCT[A/T]AGACAATCCAGATAA | 10580 |
rs576757818 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440346 | CAGAGGTCACTGACA[A/C]CACTCACGAAATACG | 10580 |
rs576780075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339647 | CCCAATCTTCATTTC[C/T]AAGGCAAAGATTTTG | 10580 |
rs576801979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95466226 | GTGGGCTAATCACGA[C/T]GTCAGGAGTTCGAGA | 10580 |
rs576813391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95458039 | AAAAAAAAGCATTTC[A/G]GGGCTGGAAAAAAAC | 10580 |
rs576827295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95537027 | CTAATCACAGTGGGC[C/G]TGCAGGTGCCCAGCA | 10580 |
rs576834421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95464632 | TTCTTCTCCAAGCCA[C/T]GCATAACTCTCTGAA | 10580 |
rs576850426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410004 | AACCAGAAGCAGTCA[A/G]AGACACTACAGAAAA | 10580 |
rs576869129 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512955 | GGGGTCAGGGCGAAG[C/T]AGTGGACCAGTTCTC | 10580 |
rs576870446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95538750 | TTTGGGAAGCCAAGC[C/T]AGGAGGATCACTTGA | 10580 |
rs576874981 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521423 | ATCTTCCTTTCTCTC[C/T]TAGCATTTTTTTTTT | 10580 |
rs576894323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95536517 | TCCGGGATCCCTGAA[C/T]TTTAGAATGGGTCTA | 10580 |
rs576912292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95402220 | TTTTACTTGAAAGCT[G/T]GTGGTCATGTGACTC | 10580 |
rs576924816 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480215 | TATTTACTTAGAAAC[A/C]GTTGCTGATGCTTAC | 10580 |
rs576926495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395501 | TTTCAAATACCTCTG[C/T]CTACCATTAAGGCAG | 10580 |
rs576930296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95431648 | ACAATAATCCTGAGG[C/T]AGATGCAATTATCAA | 10580 |
rs576930906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95502480 | ACTCCAGCAGATCAG[A/C]CCCAGGCCCCCTGCC | 10580 |
rs576961083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95530278 | CAGGTGTTCCTTCCT[A/G]CCTCTCCCAGAGGAC | 10580 |
rs576990325 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446719 | CACGGCCTTTGCTCT[C/T]GCCTCTGTTTAACCT | 10580 |
rs576991524 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95487816 | AGAACTGATTTTCTC[A/C/G]TATCAGTCAATGGCA | 10580 |
rs576998078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432104 | CTAGCCCATCGCACC[A/G]CTTACTTACCCCCCA | 10580 |
rs577005189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95495877 | GGCTGACCAGTTTGG[A/G]AAGGAAACAAATCAG | 10580 |
rs577017713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95359489 | AATCCTCCCACGTTG[C/T]CCTCTAAAAGTGCTG | 10580 |
rs577036825 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SORBS1 | GRCh38.p7 | 10:95448413 | CTTTCAATTCAACCT[A/G]GGTCAAATTTCAATG | 10580 |
rs577051291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95347828 | CACTGCAGTCTTGAC[C/T]CCCCAGGCTCAGGTG | 10580 |
rs577069706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95480870 | GGGTTCCAGCAGAGG[A/G]GAGGGCAGACAGCAA | 10580 |
rs577071654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95425939 | TCCCAAGCTGGGGGG[A/G]GTGCCTCGGAAAGTT | 10580 |
rs577125876 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467529 | TGTGTGGAAGCAACA[G/T]GAAATAAAGGTTTAC | 10580 |
rs577131112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95557716 | CTCAGTCCACCCCCC[A/C]ACCCCCCATCCTAGG | 10580 |
rs577156056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95459943 | TGCAAAACCAAAATG[C/T]TGCCTAGTCAAGTAC | 10580 |
rs577160206 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452695 | TAGGTTGGCATTATA[C/T]ATTTATATATTAATA | 10580 |
rs577182917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395898 | CACTTTGAACCCAGC[A/G]GGAGTTAATTAACAG | 10580 |
rs577182997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524352 | AAAACCTCCTATGAT[C/T]CACTTGTAGATAAGA | 10580 |
rs577191012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95320576 | GTAGAGACAGGGTTT[C/T]ACCATGTTGGCCAGG | 10580 |
rs577195432 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486263 | TTGGATTGCTTTTTA[A/G]TTTGTCTGAACTCCG | 10580 |
rs577243360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95504257 | TCTTCCCAGCTCACA[C/T]TAAATGCCAATTAGA | 10580 |
rs577245223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95523873 | ACACCAAAATGTTAG[C/T]AGGGATAACACTGGA | 10580 |
rs577248350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95511975 | ACCCCCATCCTACAC[A/G]TACAGGATTTTTTTG | 10580 |
rs577253701 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95477077 | GTTTGGCGGCCTGAG[-/T]CCCCCCGGGACAAAC | 10580 |
rs577265908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95326364 | CTTGGTCTCAGGCCA[A/T]GCCCAAAGCTAAGGA | 10580 |
rs577288819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375288 | TTTATATTCCTTTGG[A/G]TGCAAGGCTAAGAAA | 10580 |
rs577321355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95348699 | CAGTATTGTATTACT[C/T]ACTACAGGACAGAGA | 10580 |
rs577323825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355767 | TGAGAGGGCTCTGAG[C/T]TGCGGCTAAGCCTGG | 10580 |
rs577331024 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95411616 | ATGCTCTTCTTAAAA[C/G]GCTTTAAGAACAAGA | 10580 |
rs577350641 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383236 | CCTAGCCAACACGGC[A/G]AAACCCTGTCTCTAC | 10580 |
rs577354940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95525455 | TTTATAGTGAAAAGT[C/T]CCTATTCCACCCCCA | 10580 |
rs577368314 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532343 | ACCTTCCCGGCCTCT[C/G]GTTCCTGCTCCTTCC | 10580 |
rs577372015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421015 | TCCTTTAAGAGAAAG[A/G]ACTAGGCTAGGTGTG | 10580 |
rs577380675 | snp | C/T | 0.000164989 | 0.00908116 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397184 | ACGTGTATTGGCACA[C/T]AGCACAGCACAGCTT | 10580 |
rs577407682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95417998 | AGTCTGATCAATATC[A/G]GTAAGTGAATTTTGA | 10580 |
rs577418162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95460477 | AGCACTTTGGGAGGA[C/T]GAAGCGGGTGAACCA | 10580 |
rs577419385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95550822 | TTTCTTAATGAAAAA[A/C]GAGACCCCAGCAGAT | 10580 |
rs577423880 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95500301 | AATATCCTCTCCTCA[-/G]GTGACACCCATGCAG | 10580 |
rs577428247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95531980 | ATGCCCTGAGATTTC[A/G]TCCCATAAGAAATAC | 10580 |
rs577432738 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444151 | ACCCAGGCTTGAGTG[C/T]ACTGGTGTGATCACG | 10580 |
rs577439376 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314320 | GCCTCCAGAGCCACA[A/G]GGCTTCCTGACTTCA | 10580 |
rs577485684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355153 | TTTTGGATTTATTTG[C/T]GAACTAGTTTAATGC | 10580 |
rs577491597 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SORBS1 | GRCh38.p7 | 10:95446451 | TGGGAAAGGAAAGAA[G/T]GTCCTTATATGGGTA | 10580 |
rs577498102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95545315 | CAGCAACTCAGATCT[C/T]CCAGCTCCAGTTCCA | 10580 |
rs577514624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405136 | CATCACCAGGGAGCT[A/G]GGCAGAAATGCACAT | 10580 |
rs577529079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95482465 | TCAGAAATATTCTGC[A/G]GGATGACAAGAAGAT | 10580 |
rs577533520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95426974 | TCTAATTTAATGGAG[G/T]TACGGGGTACCTTCA | 10580 |
rs577553269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95544798 | CAATGATGCTTCAGG[G/T]GAGTATTTAAATAGC | 10580 |
rs577556471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95513761 | AGATCTCCCTTGGCC[A/T]CATGGGACCATCTAG | 10580 |
rs577559431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95551316 | TTTCCCCATGGAGGC[C/T]CCCAGAATGCAGGAA | 10580 |
rs577579621 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409493 | AACTACTAAAACAAC[C/G]TTAAGATTTTAGTGG | 10580 |
rs577588647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441205 | AACAAACACCACACA[A/G]TGCAATTGATGAATG | 10580 |
rs577592847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540389 | GAGTCAGAAATCTGA[A/G]TAAAATGAAATCCCA | 10580 |
rs577610853 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332958 | GGGGGAGGCTGTCAG[G/T]AAAGGTGTTAAAGGA | 10580 |
rs577631383 | in-del | -/TG/TGTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378737 | GTCCTACTACATATA[-/TG/TGTG]TGTGTGTGTGTGTGT | 10580 |
rs577648970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434445 | GGCTCTCAGGAAAAC[A/G]CACACAGACATTCAC | 10580 |
rs577658137 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313286 | CTGTGGCTGTCTGGT[C/G]GGGGATGGGAAGCTG | 10580 |
rs577683085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95335637 | TGCTATCATCTCCAT[C/T]TTACAGATGAGGAAA | 10580 |
rs577729475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95540831 | AATTTCCTTTCTGCA[A/G]ATTCAGGAAGATTAA | 10580 |
rs577746970 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95454908 | CAGGCACATGCTGAC[A/C]AAAGCACCAAATAGC | 10580 |
rs577761670 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95405667 | GGACCCACCACCCCA[-/G]GGGCATCTACTGGCA | 10580 |
rs577762637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95512973 | TGGACCAGTTCTCAT[A/C]GAAGAGCAGCAAGAT | 10580 |
rs577772612 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528685 | GCACTTTGGGAGGCC[A/G]AGGTGAGTGGATCAC | 10580 |
rs577782577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337703 | CCTGACCCGGAACCA[C/T]ACGGGGAAAGGTGGC | 10580 |
rs577814840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95440370 | AAATACGGCAGGATT[A/G]GGAGACTCCGGAATG | 10580 |
rs577824616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377147 | AAAACATTGATAATC[A/G]CAAAAAGAGAGTTGG | 10580 |
rs577851006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95358213 | AAGCTCTCTGTCAGA[C/T]GTGCCTCTGTCACGT | 10580 |
rs577867336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95328562 | AGTTGGGGGGTAATG[G/T]CAGATACATATTCAA | 10580 |
rs577895096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95329253 | TTTTTTTTCTATTGT[C/T]CAGACTAGAGTGCAG | 10580 |
rs577898613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95461920 | TTTCTAAGCCTGGAT[A/G]TTTAGGAAAGCAAAG | 10580 |
rs577899127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95505913 | TGAGAATGAATTCCA[A/G]AGCAACCATGCTTTT | 10580 |
rs577903578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322473 | ACTTTAGGGTAGAAA[G/T]GCAAGTATGTATCCC | 10580 |
rs577904650 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344984 | ATTGTTTTAAGACTC[-/TT]TATGAAATCTGGGAA | 10580 |
rs577906071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95560466 | ACAGCACATTCCCCC[A/G]TGAAGGAAACATAAT | 10580 |
rs577909342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499395 | ATTTTTAAATTACAA[C/T]AACATTTATAAAGCC | 10580 |
rs577914216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95435153 | CGAAGGAACAAGATC[A/G]TGAGTTGTCTGGTCC | 10580 |
rs577936251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95352956 | GTTAAACATAATCAG[C/T]GGAAGTGGACATCGA | 10580 |
rs577951328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95467918 | TTTTTTTTTTTTGAG[A/G]CAGAGTTTCACTCTT | 10580 |
rs577955228 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407389 | GCTGCTGAGCTCCAG[C/G]TGGCAGAAGTGAATG | 10580 |
rs577967033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399472 | CTAAAATATTTATCA[C/T]CTGGTCCTTAAAAAA | 10580 |
rs577979946 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353959 | CAACAGAGAAAAAGG[C/G]CTTCAGACTTGAACG | 10580 |
rs577999316 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95350991 | GTGCCAGCAGATCCC[A/C/G]GTCCCCCAGCCAGGC | 10580 |
rs578001747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344169 | AGAGACGAACTGAGG[G/T]GTCTGTAGTTGTAGC | 10580 |
rs578034744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95524148 | CCAATAATGGTTCCC[A/G]GCAAAATTATAGAAC | 10580 |
rs578036529 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95338993 | GATTACAGGCATGAG[C/T]CACCACACCCGGCCT | 10580 |
rs578037756 | snp | C/T | 2.57808e-05 | 0.00359023 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384379 | AGTCTGGTACGAGCA[C/T]CCAGCCCCCCTAGGG | 10580 |
rs578043889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95533789 | GCAAACAGGCTCACG[A/G]CCACATGACTGGCCG | 10580 |
rs578048250 | snp | A/G | 1.70525e-05 | 0.00291992 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357589 | TCAGTGAATGGAGGT[A/G]GATGGGAGACAGAGG | 10580 |
rs578051062 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557063 | TCCACATGCCTAACC[A/G]CACACAAAAAGGGGG | 10580 |
rs578056875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95447755 | GGATAAACACTGAGT[C/T]GCTGATACTTCCGTT | 10580 |
rs578075414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95392508 | TCATCTTTGCTATTA[A/T]TTTTTTTATATCCAA | 10580 |
rs578080357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SORBS1 | GRCh38.p7 | 10:95499016 | GGGGTGAAGGGCACA[C/T]AGGATCCCTCTGTAC | 10580 |
rs578114788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95527014 | GAACCTAAAACAGTC[A/G]GTGCTCAATACATAC | 10580 |
rs578124025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95378894 | GATCTCCAATTCCAA[A/G]GCTAGAAGAGAAAAA | 10580 |
rs578150668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357052 | TAGTGTTAAACGTTC[A/G]GCTATGGACTGAAGA | 10580 |
rs578172766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95344729 | TGCTTTTTTGAGTAA[C/T]TGACTATGGCGAAAT | 10580 |
rs578192645 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412886 | AAGGATATCCAAGGC[C/T]GTGGGTCACATTGGG | 10580 |
rs578214524 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461663 | GAAATGTTCACTAAT[A/T]TGTACCATCACTTTA | 10580 |
rs578217585 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386247 | ATTTAAATATTCAGG[G/T]TTTTTTGTTTTTTTT | 10580 |
rs578234556 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503642 | TTTGGGAGGCAGTGA[A/G]GACTAAAACAGAGAA | 10580 |
rs578240643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95521360 | AGGAGCATGTCAGCC[C/G]TAAGTCATCCTTTTT | 10580 |
rs578242479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SORBS1 | GRCh38.p7 | 10:95393324 | AGACCAAAAATGGCC[C/T]ATGGTATTTTAACTG | 10580 |
rs578259305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95520615 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 10580 |
rs745319360 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95359677 | GTTACTCACCATGAA[C/T]ACACCCCTAAGATAA | 10580 |
rs745326658 | snp | C/G | 5.28341e-05 | 0.00513948 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414876 | TCCTGTGGAAATAAG[C/G]GGGTCGTTATGGAAA | 10580 |
rs745327328 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484273 | TCTCTTGATTTTTTA[G/T]GATAAGATTTTAAAC | 10580 |
rs745333337 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377293 | CCATGTGTGGTGTGC[A/G]GGTCTTTAATGCTAG | 10580 |
rs745336034 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442376 | TCCCTGCCCAAATCT[C/T]ACATTAAAATGCAAT | 10580 |
rs745338274 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521218 | TTTGTCTTCCCAGTC[A/G]CCAATGGCCATGATA | 10580 |
rs745342313 | snp | C/T | 3.43212e-05 | 0.00414239 | missense | SORBS1 | GRCh38.p7 | 10:95339155 | CTTGCAGTGGCACTG[C/T]GACTTGGGGAGGAGG | 10580 |
rs745342355 | snp | C/T | 1.65466e-05 | 0.00287628 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397330 | AAATGACTATCTTGA[C/T]ACATTTCAGACCTCC | 10580 |
rs745347873 | in-del | -/CACACG/CACG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554717 | ACACACACACACACA[-/CACACG/CACG]CGCGAAAGTTTTATA | 10580 |
rs745386363 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403536 | AGGAATAAGCCTGAG[C/G]TGCCAGCACGGTGGA | 10580 |
rs745393207 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552247 | TCTCTACTAACAATG[C/T]AAAAATTAGCTGGGC | 10580 |
rs745405117 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430882 | TCTGTTGACTTTTAG[G/T]GCTGTGGGCTGCTCG | 10580 |
rs745410311 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318915 | CATGTGCAGTTCACA[A/G]TAGGGTTCACGCTCC | 10580 |
rs745417469 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465492 | GAGATCACGCAACTG[C/T]ACTCCAGCCTGGGCG | 10580 |
rs745419554 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330636 | ATGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10580 |
rs745432276 | snp | C/T | 3.40559e-05 | 0.00412635 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95354957 | TATAAAATGTCTTGG[C/T]GATTCTGAATCTTTA | 10580 |
rs745447146 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540014 | TTGTCTAAAAACATA[C/G]TTTTACACAGGGAGC | 10580 |
rs745453424 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512160 | TGGTGGCTCACGCTC[A/G]TAATCGCAGCACTTT | 10580 |
rs745464028 | snp | A/G | 2.12276e-05 | 0.00325781 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336503 | GCCAAGTGCACACGC[A/G]GCATGCTGCAGTCCT | 10580 |
rs745466710 | snp | C/T | 1.64923e-05 | 0.00287156 | missense | SORBS1 | GRCh38.p7 | 10:95339237 | TCACATCCACGTAGG[C/T]GATGGGGAAGATGCC | 10580 |
rs745488063 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512984 | TCATCGAAGAGCAGC[A/T]AGATGAGACAAGTTT | 10580 |
rs745503674 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500819 | TCTATGATGTTAAAC[A/G]AGTTCTCAATCTCTG | 10580 |
rs745507215 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390796 | GGCGCCTGCCATCAC[A/G]CCCACTGGCTAATTT | 10580 |
rs745509312 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379147 | CACTTTGGGAGGCAG[A/G]GGTGGGTGGATCATT | 10580 |
rs745518105 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471778 | GCAGTGACAGGAGGA[A/C]GTGGAAGGCAGGAGA | 10580 |
rs745531978 | snp | C/T | 4.94491e-05 | 0.00497213 | missense | SORBS1 | GRCh38.p7 | 10:95381737 | TGATATTCGTAAATG[C/T]TCTTGGGCTCTGCAC | 10580 |
rs745532377 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95399086 | CTTCACCACCCGCCT[A/G]CTGTCATCCTTTGCT | 10580 |
rs745546246 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360746 | CTAAAGTTTTTCTTT[C/T]AACAGAGTGACTGAC | 10580 |
rs745556452 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343202 | TTTTAACCAGGACTC[-/T]TTTAAAAAAAAAAAT | 10580 |
rs745573203 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459928 | GGGTTGCCTCGGAAC[C/T]GCAAAACCAAAATGC | 10580 |
rs745601041 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380186 | CCAAGAACTGTGGTA[C/T]GGAAGATCCTGGTAA | 10580 |
rs745605328 | snp | C/G/T | 6.59886e-05 | 0.00574376 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95432485 | GGTTTCCTGAGGGCT[C/G/T]GCAGGGCTACTGCTT | 10580 |
rs745606323 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448685 | GCAGATGTGGTCCAT[C/T]TAAATATAGTACAAT | 10580 |
rs745609002 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502182 | TGGAGAACAAAAATT[A/C]AAATATCCTTCCCCA | 10580 |
rs745625984 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409355 | CCAGTAAGGGGCATG[A/G]CACCGCTGAAGGAGA | 10580 |
rs745634891 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95420829 | AGTGCATTTTTACAT[A/C]CTCACAACAGGAACC | 10580 |
rs745664006 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541077 | CAATGTGTTTCTCCT[C/T]TCACCTCTAAGGGAT | 10580 |
rs745678461 | snp | A/G | 1.73123e-05 | 0.00294208 | stop-gained, intron-variant | SORBS1 | GRCh38.p7 | 10:95336559 | CTTTCCTCCCCGCCT[A/G]CTCGCCACCTCTATG | 10580 |
rs745698630 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558944 | AAGGACACAGGCCCA[A/G]AGAGCAGAAGCCACT | 10580 |
rs745708578 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337835 | TCACTCTTGGCTAGT[C/T]AAGTGAAAAATGTAG | 10580 |
rs745716925 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530178 | ACCCTCTGCATAGAA[A/T]GCCTTCCAAGACGCT | 10580 |
rs745727469 | snp | C/T | 3.39386e-05 | 0.00411924 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357605 | GATGGGAGACAGAGG[C/T]CTGCAGGCTTCACCC | 10580 |
rs745737193 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351229 | ACCCAGATTTCCTTT[C/T]TGCAGTATCGTCTAT | 10580 |
rs745741444 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361981 | TAGCAGCTGAGTACT[C/T]AACAAAACAAGTTAA | 10580 |
rs745742274 | snp | C/T | 1.76465e-05 | 0.00297034 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337000 | GTGGGGAAGGTAGGG[C/T]CAGTGGAGAAGCTAC | 10580 |
rs745752410 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327002 | TGTGTGTACTAGAAC[A/G]TTTTAAAATCACACA | 10580 |
rs745758669 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314408 | GGCAAACCTTGTGTG[C/T]GTTTCTCTCTGAACA | 10580 |
rs745778019 | snp | C/T | 1.65866e-05 | 0.00287976 | splice-acceptor-variant, intron-variant | SORBS1 | GRCh38.p7 | 10:95394675 | GTAAGGATTGTCCTC[C/T]GTAGCAGAGAAAAGC | 10580 |
rs745785275 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491463 | AATCTGAGCCAAACA[A/T]AAAAATCAGAGCTAT | 10580 |
rs745801028 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95478302 | CTTTAAGTGAGAGCT[A/T]CTCCTTTTTGGGTTT | 10580 |
rs745809728 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486373 | GCAGTGAGATGTTCA[A/G]TTGAAATGGCCATAA | 10580 |
rs745810240 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520239 | AAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 10580 |
rs745814021 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507682 | TTTGGGAGGTCAAGG[A/C]GGGCGGATCACCTGA | 10580 |
rs745840641 | snp | A/G | 4.97187e-05 | 0.00498567 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357761 | ATCCCCAGGAGCCCC[A/G]TCTGATTCCCTCTTC | 10580 |
rs745849308 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95563003 | GTATTTATTGAGCAC[A/G]TCTAGGCTGCTATGC | 10580 |
rs745898420 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457798 | CGACAGGACAGCAGT[A/G]CCCTTGGCTGTCTGC | 10580 |
rs745902313 | snp | C/G/T | 3.29882e-05 | 0.00406118 | splice-donor-variant | SORBS1 | GRCh38.p7 | 10:95441125 | GTTTAAAATGACTTA[C/G/T]CAGAACTCATGGTGG | 10580 |
rs745905748 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435050 | AAGGGGAGAGCACTC[A/G]GGGTCCACAGGGCCT | 10580 |
rs745915160 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429513 | ACTTATTCTAGTCTG[C/T]GTTGTATACTTAATG | 10580 |
rs745920286 | snp | C/T | 1.65888e-05 | 0.00287996 | missense | SORBS1 | GRCh38.p7 | 10:95318427 | TATAATGCTTGATAG[C/T]TAAATCTATACATGA | 10580 |
rs745947604 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445847 | ATTTAGAGATAATAT[A/G]GGCCATTACAATCAG | 10580 |
rs745961235 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433956 | CAGCCCATCCATAGG[C/T]TCCTGGACACACAGC | 10580 |
rs745973253 | snp | C/G | 1.67262e-05 | 0.00289185 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375942 | AGCATTAGTTTAAAA[C/G]GTGTATAACCACTGA | 10580 |
rs745976008 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458838 | CAAAAAGTCTGACAG[A/G]GGGCATGTTAAGAAG | 10580 |
rs745987920 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376692 | AAGTAAAGACAGAGG[-/AC]ACAGTGAAAAAACAT | 10580 |
rs745998884 | snp | C/G | 1.65195e-05 | 0.00287393 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394986 | CAACAGATATGCTGT[C/G]TAAGTTTATGGTACC | 10580 |
rs746002776 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538473 | CCCTCAGGAGACGGG[C/T]TGCTCTGACTGACCA | 10580 |
rs746013893 | snp | A/G | 1.79796e-05 | 0.00299825 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337086 | GAGGGACTGGCCCTT[A/G]GTGACAAGGCGAGGT | 10580 |
rs746048736 | snp | A/G | 0.000115522 | 0.00759919 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321948 | TGAGAATCGAAGTTC[A/G]CCAGGAGTACTTACA | 10580 |
rs746051559 | snp | C/T | 1.65198e-05 | 0.00287395 | missense | SORBS1 | GRCh38.p7 | 10:95422014 | TGTAGCCCTTGGCAG[C/T]GAGTGAAGAGGGCTG | 10580 |
rs746056170 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527566 | ACAGAAATGTCACAA[A/G]GCAACTATACACCCC | 10580 |
rs746085017 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470001 | AACTACATCCATCTG[C/T]AGGGGTACAGGAGAT | 10580 |
rs746090888 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406069 | GGTGACCGGAAGACG[A/G]TTTCAACAGGAACAG | 10580 |
rs746093980 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516773 | TCAAGTGACTATTTC[C/T]AAGACCATCTTCCAT | 10580 |
rs746117573 | in-del | -/AGTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322433 | TAAAAGCCTGAAATT[-/AGTG]AGTAACTGTCACAAA | 10580 |
rs746165386 | in-del | -/CA | 1.66561e-05 | 0.00288579 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371947 | ACCAAGGCTAGAGAG[-/CA]CACACAGTCCAACGG | 10580 |
rs746174461 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476970 | TCCAGGCACCAAGAT[A/G]GAGCTACTCCTTTGA | 10580 |
rs746176682 | snp | C/G | 8.32702e-05 | 0.00645199 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406195 | TTTATACAGCACATA[C/G]TAAGACCAAGAAGCC | 10580 |
rs746190508 | snp | C/T | 4.94344e-05 | 0.00497139 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336691 | TACTCAGGCACCTGA[C/T]CACGTCTGAAGGCTT | 10580 |
rs746193368 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382782 | TGTGATTAAGTTTTT[A/C]ATGCAAGGCTGTAAA | 10580 |
rs746199424 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463461 | AGAGCTAATGAGGAT[A/G]CTTCACATTGTTCAC | 10580 |
rs746204089 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | SORBS1 | GRCh38.p7 | 10:95341355 | GCTTCTCCATATTCC[A/G]AAACCTGCACTGGTG | 10580 |
rs746212771 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557527 | CCTCAGCATCAGCCA[C/G]CATCACCACCCGCAC | 10580 |
rs746214392 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366030 | CAATGTAGGTAGGAT[-/A]ATGTCCCAGAGACCA | 10580 |
rs746226943 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464408 | GGGCAAATTATCTTG[A/G]TGTCTTCATCTGTAA | 10580 |
rs746227234 | in-del | -/AAGA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418731 | CATACAGGTGGCAAG[-/AAGA]AAGAATGTTAGAAAG | 10580 |
rs746232956 | in-del | -/CCG | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442523 | TGTGGCACCCCCCCC[-/CCG]CCGCACCCTTACTTA | 10580 |
rs746235763 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452269 | TCTTTTCTGAGAAAA[C/T]CTCTCTTCTCGGTGG | 10580 |
rs746235906 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407492 | GGCGTGGTGGCACAC[A/G]CCTATAATCCCAGCT | 10580 |
rs746239097 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388470 | GTTAAGACACATTAA[A/G]TGAAATGTTTCTCAA | 10580 |
rs746261170 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424930 | TACATGAAAATACCT[C/T]TGAGTGCACCACACT | 10580 |
rs746282023 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533360 | TCACGAGTTTTGGGT[C/T]CACCAGAGAGTAATA | 10580 |
rs746290064 | snp | C/T | 1.69706e-05 | 0.0029129 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341238 | TTCCCCACATAGCTG[C/T]GCCATCCAAGAGAGC | 10580 |
rs746292295 | snp | A/G | 0.00012119 | 0.00778334 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356373 | GCCGAGCGGGCTGAG[A/G]TCAGGCTGCCCCGGG | 10580 |
rs746298864 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412757 | AGATGCTTGAACTCC[C/G]CAAAACAAGAGTGGC | 10580 |
rs746313853 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353848 | TCACCATCTGGTGGC[A/T]ATAATTATCATCATC | 10580 |
rs746314270 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520658 | AAAAGCTTATAAATG[-/C]CTAAATATACTTCAG | 10580 |
rs746334900 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534197 | CAACCTCCACCTCCC[A/G]GGTTCAATCGACTCT | 10580 |
rs746336713 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336758 | GCCTCTTTCGCCTGC[C/T]CCCCTCTCTGCTTTC | 10580 |
rs746337725 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493641 | GGAGTAAAGACCAAA[C/T]ACGTGGTCAAGGGTA | 10580 |
rs746337893 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329120 | AGAGATGCTCACCAA[C/G]AGGTCACCTTAATTT | 10580 |
rs746345123 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366646 | TCTATGTGAGAATCA[A/G]GTAAATTAGCCCCTT | 10580 |
rs746360074 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432332 | CACACACACACACAC[-/C]ACCCCCCCCCCCCAA | 10580 |
rs746368989 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514331 | CAGTGGAACAGTGTT[G/T]GACCAGCTCCCTTCC | 10580 |
rs746370767 | snp | C/T | 4.55446e-05 | 0.00477182 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384368 | CCCATTTCCACAGTC[C/T]GGTACGAGCATCCAG | 10580 |
rs746372918 | snp | C/T | 1.75486e-05 | 0.0029621 | missense | SORBS1 | GRCh38.p7 | 10:95367690 | CCGGAGTAGGGCTGA[C/T]GGCTGAGCTCTGTAC | 10580 |
rs746384344 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454272 | CACTGATTGTGTATG[C/T]ATTCTGTGCAAGGCC | 10580 |
rs746389377 | snp | C/T | 3.30136e-05 | 0.00406273 | missense | SORBS1 | GRCh38.p7 | 10:95384258 | TCAGAAAATGAGTAT[C/T]TGGGAGAGTACAGAT | 10580 |
rs746392453 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483119 | GCTTTCTTGGTGGTG[C/G]TGGTGGTGTGAAATT | 10580 |
rs746396103 | in-del | -/A | 8.93599e-05 | 0.00668371 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339094 | ACTACAAAAATTCAC[-/A]TGCTGAGTATGAAAA | 10580 |
rs746418412 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495247 | TTATATTCTGGCCTA[A/C]AACAAGACATTTCTC | 10580 |
rs746433849 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453813 | ACTTTTCCTATATGT[A/G]AGTACTGCAGGGCCC | 10580 |
rs746441202 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547577 | TCTCTACTAAAAATA[-/C]AAAAAATTAGCCGGG | 10580 |
rs746451304 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369933 | TCCTTCAAGTGCTGA[A/G]GGAGAGCTTGAGCCT | 10580 |
rs746481876 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399943 | GCTCTGCCTTGTGGA[C/T]ATGAAGGTGAGCATT | 10580 |
rs746520663 | in-del | -/AT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473677 | TATGAACTACATATA[-/AT]ATATATATATACACA | 10580 |
rs746532237 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411523 | ATAAGACCCCAAAAG[G/T]TACTAAGAATATTTA | 10580 |
rs746542011 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533982 | TGTCTAGAAATCATT[C/G]TTTTTGAAATGTCAA | 10580 |
rs746543918 | snp | C/T | 1.70046e-05 | 0.00291582 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399229 | CTGAAGCTCTTTTGG[C/T]AGCTGCAAAACAAAA | 10580 |
rs746544985 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95441002 | ATGACAAAGCTTTGG[C/T]ATTCACCCAGGTGGC | 10580 |
rs746560507 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328254 | TCCTGGGTTTGAGCT[C/G]CAGGAAACCACCAGA | 10580 |
rs746565620 | snp | C/G | 1.67315e-05 | 0.00289231 | intron-variant | SORBS1 | GRCh38.p7 | 10:95383970 | TGAATGAATGAGAGA[C/G]AAGCGGGCACTTACC | 10580 |
rs746567491 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412670 | TCAAACTACTCACAA[G/T]GGTCTATGAGGACAC | 10580 |
rs746581028 | snp | A/C | 1.64958e-05 | 0.00287187 | missense | SORBS1 | GRCh38.p7 | 10:95339245 | ACGTAGGTGATGGGG[A/C]AGATGCCTTGTCGGG | 10580 |
rs746593892 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522494 | TCCCACTAGTGCCCA[A/C]CAACTTCATGTCAAT | 10580 |
rs746594365 | snp | A/G | 3.31713e-05 | 0.00407242 | missense | SORBS1 | GRCh38.p7 | 10:95357765 | CCAGGAGCCCCGTCT[A/G]ATTCCCTCTTCACTG | 10580 |
rs746595245 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523307 | TTATTAGATTCTCTA[C/T]TTCATCCTCAGCTAC | 10580 |
rs746615955 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336650 | GCTCTCCTCAGGGGT[A/G]TTGAGATCTGAGAGT | 10580 |
rs746622921 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318843 | GGATGGTTTTGGGAT[A/G]AAACCATCAGGACAT | 10580 |
rs746630102 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374515 | CATATACCAATCATG[A/G]TCTGTTTTGGGGGTG | 10580 |
rs746634419 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510966 | ATTTATCTCGTTCCA[A/T]GCAAGCCTGTCTTTG | 10580 |
rs746639208 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348364 | AGCTGTAGAGCTGTG[C/T]GAACTTTAAAAAATG | 10580 |
rs746647543 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482893 | ATACCAACAGTCTGA[A/T]GAACTCTCACCCCAA | 10580 |
rs746649285 | snp | C/G | 1.64784e-05 | 0.00287035 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95432548 | AGTCACCGCTCCCTT[C/G]CCAGTGCAGATTTTT | 10580 |
rs746655015 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388375 | GTTAGAAATACCAAG[C/G]AATGGGAAAACAGTG | 10580 |
rs746666711 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384056 | CCTCTTGACTACCTT[C/T]TCACCATCAATGTAG | 10580 |
rs746694657 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371122 | CCCCTTTAAGGAAGA[C/T]GCCAAGCTCAAAAGA | 10580 |
rs746698253 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461711 | GTACTGATCGCGTCA[G/T]AATTGCATTAAGCAG | 10580 |
rs746703470 | snp | A/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442219 | ACTTCTGAAAAGCAA[A/C]TGGTTAGATATGGCT | 10580 |
rs746725683 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377956 | TTCCCAAAGGTTGTC[C/T]GCAGATCGTTTTACT | 10580 |
rs746746823 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389355 | GGAAGCCCAGAGAGC[G/T]TGGGGGAAAGCATTA | 10580 |
rs746754995 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528219 | CACCTGGGTAATGTC[A/G]AGGGCTTCATTAAAA | 10580 |
rs746766513 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538728 | AAAAATAGCACAATT[A/G]CAGCATTTTGGGAAG | 10580 |
rs746778047 | snp | A/G | 1.79806e-05 | 0.00299833 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414584 | AGGTGGTGGTGAGAA[A/G]GATGGTGGCGTCTGG | 10580 |
rs746782552 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430580 | GGAGCTCCAAGCTCC[C/T]TCTCCACCACCTCCA | 10580 |
rs746808422 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551806 | CAAGTATTCAGAGAA[A/C]TAGGGAGCTCTTACA | 10580 |
rs746821131 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459875 | AAATCATCCTTCGAG[C/T]GTGCCTCTTCCAATG | 10580 |
rs746837610 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419283 | AAATGAATAGCCCCT[C/T]TCTAGTATTCAGCAA | 10580 |
rs746841941 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554764 | TTAAAAAGAGAAGAA[-/AC]ACAGACTCACTCTAT | 10580 |
rs746847534 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411048 | GGTCCACCTGTTAAC[-/A]GTTGTGGGTCAATCT | 10580 |
rs746859637 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539686 | CGATGGCAGTTACAT[A/C]AAATGACATGTAAAG | 10580 |
rs746862126 | snp | A/C | 1.87876e-05 | 0.00306488 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367632 | AAGCAATGTAAACAA[A/C]ATAAAATGGCAACTT | 10580 |
rs746862244 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351240 | CTTTTTGCAGTATCG[C/T]CTATATTGAGGAGGT | 10580 |
rs746863330 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499732 | CATTCCTAACAGTTT[G/T]GTCTTCAATCTCTTA | 10580 |
rs746870081 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444857 | ACATTTCACATTTCT[C/T]AATATAGAAACTACT | 10580 |
rs746871175 | snp | A/G | 1.75727e-05 | 0.00296412 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337161 | GGGGTCAGGGCCAGA[A/G]AACGCCTGCCTGGGA | 10580 |
rs746892109 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373012 | CTCCATGGAAGCATT[-/C]AAATTGGTTTACATT | 10580 |
rs746908044 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484040 | ACCAGCCTGGCCAAC[A/T]TGACGAAACCCCATC | 10580 |
rs746909815 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426216 | CTTGATGTGTTCTGG[C/T]AAGAGTATTTAAGAG | 10580 |
rs746918382 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500831 | AACGAGTTCTCAATC[G/T]CTGATGTTCAGTTTC | 10580 |
rs746934899 | snp | G/T | 5.01048e-05 | 0.00500499 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376082 | TGGTGATAGAGAAAT[G/T]GAAGAAAGAGAAGGA | 10580 |
rs746936677 | snp | C/T | 1.65754e-05 | 0.00287879 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395117 | GAGAATAGAGGAAGA[C/T]ACAAATGGAGAGAAT | 10580 |
rs746946791 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490249 | AACTGTGAAATTCTC[C/T]GATCTCAAATAAAAA | 10580 |
rs746978438 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335437 | AGACATACTAGATAC[C/T]TAATAAATGGCTTGG | 10580 |
rs746997123 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477139 | CGACCTCCTCCTCTT[C/T]TCCCTTCCCCAAATA | 10580 |
rs747002585 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448626 | GAGACCAACATGATC[A/C]GACAGGATTGCTGTC | 10580 |
rs747006022 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366327 | AGTATATGTCAGGTA[C/T]ACAGCAACAGAAGTA | 10580 |
rs747009996 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534483 | TCAGGGGGCAGAGAC[C/T]GTGTGGTGTGGATAA | 10580 |
rs747026054 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407767 | AACATGGTAAAACCC[C/T]GTCTCTACAAAAAAT | 10580 |
rs747036722 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439603 | TGAGTTACGAAGCAG[G/T]AGCTACTGGCAGTAC | 10580 |
rs747037816 | snp | A/T | 1.65282e-05 | 0.00287469 | missense | SORBS1 | GRCh38.p7 | 10:95422023 | TGGCAGCGAGTGAAG[A/T]GGGCTGGGCATTTCC | 10580 |
rs747063017 | snp | A/C/T | 3.29735e-05 | 0.00406028 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95321971 | TACTTACAAATCTTG[A/C/T]GAGGTTTGACTCCTG | 10580 |
rs747063549 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427293 | CACTCACCACCAACT[C/T]AGGCTCCCTGTCTGG | 10580 |
rs747068728 | in-del | -/AAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383418 | AAAACTCCGTCTCAA[-/AAAA]AAAAAAAAAAAACTC | 10580 |
rs747100857 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456339 | TTAAGAGGTGATTAG[C/T]TCATAAAGCCTCTGC | 10580 |
rs747124940 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536759 | ATGGCCCACTGTGAA[A/G]CCTTCAGGGGTGCCA | 10580 |
rs747126267 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391307 | AGATAACAATAGTGA[C/T]ATATTCAGCACAGAA | 10580 |
rs747135040 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315249 | CTTAGAGAATACCGT[A/G]TGGTTTCCAAAGTAC | 10580 |
rs747167990 | snp | A/G | | | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95416146 | ACTGCCATGCAAAGC[A/G]GTCCTTTTGAGGGAG | 10580 |
rs747174126 | in-del | -/AAAA/AAAAG | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562780 | ATTAAAAAAAAAAAG[-/AAAA/AAAAG]AAGAGTCCTAGCCAT | 10580 |
rs747192890 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333300 | TCTCCCTCCCATAAC[A/G]TGTCTTGCTGCTTAA | 10580 |
rs747200558 | in-del | -/G | 7.82564e-05 | 0.00625477 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422225 | TCCAGACCTACACGT[-/G]GTGCAGAAAGGATGA | 10580 |
rs747204443 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544785 | GGAAAATTACTCACA[A/G]TGATGCTTCAGGTGA | 10580 |
rs747217716 | snp | A/C | 1.64765e-05 | 0.00287019 | missense | SORBS1 | GRCh38.p7 | 10:95410693 | TGGAGGGATAGGCGG[A/C]TGAAGGCTTGCTAAC | 10580 |
rs747240577 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375614 | CATTTTCAGCTTGTC[G/T]TTCACAGACCATAAA | 10580 |
rs747268145 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344042 | CCTCAGCATATTCAC[C/T]CCTATGGAGATCTGC | 10580 |
rs747271321 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514581 | CACCCCAGAAACATC[A/C]CGGTGAACCAAGTTA | 10580 |
rs747275529 | snp | C/T | 8.26043e-05 | 0.00642615 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434609 | GAGAAAATCGACCGA[C/T]CCAAGGAGATACCTG | 10580 |
rs747283220 | snp | A/G | 0.00109005 | 0.0233203 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356386 | AGGTCAGGCTGCCCC[A/G]GGACAGCACAGGTGT | 10580 |
rs747293723 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386426 | GTATCGCTTGAGGTC[A/T]GGAGTTTGAGACCAG | 10580 |
rs747308614 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521467 | TCTGTCACCCAGGCT[-/G]GAGTGCAGTGGTGCG | 10580 |
rs747311021 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353013 | TTGAATCTCACCTTA[A/G]TAAGTCCCTCAGCCC | 10580 |
rs747315124 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474324 | AGAAACGGAGTCTCT[C/T]GTGTCCTACAAAGCA | 10580 |
rs747318025 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457574 | TGTTCTAACTCCAAA[A/C]ATGAAGTGTGAGAAG | 10580 |
rs747331000 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323968 | CAAAGCAAGACCCTG[A/T]CTCAAAAATAAAAAA | 10580 |
rs747350418 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336870 | CTATCAGAGCTCCCC[A/G]GCGGCAGCTGCAAGA | 10580 |
rs747363074 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523286 | CAGGGCTAGGCTATC[A/G]GAGAATTATTAGATT | 10580 |
rs747395326 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434541 | ATTCAGCTCAAAGTG[C/T]GTGTTAGAAGAAAAG | 10580 |
rs747396368 | snp | A/G | 3.31351e-05 | 0.00407019 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341559 | AAGAAAAGAGGCTGC[A/G]GTACCTCGATGTAGG | 10580 |
rs747402263 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515510 | TGCTAGCCTGCTCCA[A/G]CCTGCCCTATTCTGA | 10580 |
rs747408016 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405350 | ACTCAGGAGGCTGAG[A/G]TAGGAGGATCACATG | 10580 |
rs747408430 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423693 | ATTTACAGACATTTA[C/G]TGAACACCTCTCTAA | 10580 |
rs747423734 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556131 | GGTGTCCCTTGTGGT[C/T]CACAATACAAGGGTG | 10580 |
rs747437812 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351514 | TGTCAGAACGGCTGT[A/G]GAGCCACAACTATTA | 10580 |
rs747441371 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555043 | TGCGCCACCACGCCC[A/G]GCTAATTTTTTGTAC | 10580 |
rs747445441 | snp | C/T | | | missense | SORBS1 | GRCh38.p7 | 10:95341644 | CAATTTGCTTATAAA[C/T]GTAAACAATATCTCC | 10580 |
rs747488647 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353766 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 10580 |
rs747503947 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382747 | CAAATTTTTTATTTG[C/T]GCATTACCGTACTTT | 10580 |
rs747511272 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95475370 | AACATTTACTAGCCA[A/G]GTTCCCTTCAGCCAA | 10580 |
rs747511431 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462194 | TAAGTATAGTCTTTA[C/T]GATTATTCAGCAACA | 10580 |
rs747515338 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477673 | CTATTTGCATGTCTA[C/G]GCCACAGGAAGAAGG | 10580 |
rs747524202 | snp | C/G | 1.65693e-05 | 0.00287826 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414814 | TATTAACCAGGTAGA[C/G]AGGGACAACTATTAC | 10580 |
rs747532717 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492909 | TATCAAAAATGTCAC[C/T]AATTCAGCCCTGCTC | 10580 |
rs747543841 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352616 | CCATAGAAAGAGTGC[C/T]GGTCCAGGCATCTGG | 10580 |
rs747555158 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381900 | TAATCAAAGAACTGT[C/T]ATATCCAAAGCATAA | 10580 |
rs747562860 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533121 | GTCTCACCACCATCC[A/G]AGACACAGACATGGT | 10580 |
rs747567162 | in-del | -/TCTGTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500630 | TTAAAATTAATTTTG[-/TCTGTT]TCTACTTTTTTAACG | 10580 |
rs747585396 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505074 | CCTAGGCATTAATAA[C/T]TTAATTCCCTCCCTT | 10580 |
rs747596052 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503841 | GATACCTGCCATGGG[C/G]GTCATGGCCAAATGG | 10580 |
rs747606125 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494089 | TAAATGTAAAAAAAA[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs747608600 | snp | A/C | 1.65545e-05 | 0.00287697 | missense | SORBS1 | GRCh38.p7 | 10:95432571 | AGATTTTTGTAAGAT[A/C]CATGTCTGAAAAGAA | 10580 |
rs747615031 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463158 | TGATTAAAAGAATGT[C/G]CTCAACAAATATGCC | 10580 |
rs747615961 | snp | C/T | 8.25512e-05 | 0.00642408 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434697 | CAGAAATAGAGCGTG[C/T]GCGTAAAGGGTCGGC | 10580 |
rs747624344 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335054 | TTTCTAGCAAAAGGC[G/T]AAGCCTGATTTCTTA | 10580 |
rs747630342 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491901 | TTACATGAATTAAAT[A/G]TAAGCAGGAAACTGA | 10580 |
rs747641898 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95422298 | AAACAAGCATGAAAC[C/T]GCATAGAAGGTTGAA | 10580 |
rs747642929 | in-del | -/AAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428412 | GTGAGACTCCATCTC[-/AAAAA]AAAAAAAAAAAAAAA | 10580 |
rs747644701 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462137 | GGAAAATTTCCATTT[C/T]GCATCAAACTCTTAA | 10580 |
rs747677302 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542183 | CTACCTGTTCTGTGA[A/C]TCCTTCCCCACACCG | 10580 |
rs747692640 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423602 | GGGACTAACACTGCA[A/G]TCTCACTGCCCAATC | 10580 |
rs747694390 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562113 | GGTCACACAGCAAGT[A/G]GTGCAACCAGGATTT | 10580 |
rs747696837 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531821 | GGGCCAACATGTGCA[C/T]TGTGTGACCTTAAAT | 10580 |
rs747711220 | snp | A/G | 1.65466e-05 | 0.00287628 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384232 | AGGTTATTTGAAGTC[A/G]CTTACTGTCTTCAGA | 10580 |
rs747732848 | in-del | -/TG | 1.64898e-05 | 0.00287135 | frameshift-variant, intron-variant | SORBS1 | GRCh38.p7 | 10:95336901 | AGCTATCTTGGTGGA[-/TG]CCTGAAGATGGCGTG | 10580 |
rs747735331 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442527 | GGCACCCCCCCCCCG[C/T]ACCCTTACTTATGCT | 10580 |
rs747745275 | snp | A/C | 1.64977e-05 | 0.00287203 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395007 | TTATGGTACCTTCGG[A/C]AGTTTGCTGGATTTC | 10580 |
rs747755573 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485182 | GAAAAGCCATCTTTT[A/C]CAGCAGGCACCTACC | 10580 |
rs747757776 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453984 | TGGGTCTATTCTTTG[C/T]TATCCTTTGTTTATT | 10580 |
rs747790421 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382591 | TCTTTCTCCCAATGT[A/G]TGTTCTTGGCACCTT | 10580 |
rs747805946 | snp | A/G | 6.62449e-05 | 0.00575483 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434597 | CGCTCACAGTTAGAG[A/G]AAATCGACCGACCCA | 10580 |
rs747807080 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522396 | AACACAACCCTTCAG[C/G]AATCTTATAGAAAGC | 10580 |
rs747824070 | snp | A/C | 1.65211e-05 | 0.00287407 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414682 | GGGGAATGAAATCAT[A/C]TAGAGTCGGGAAGGT | 10580 |
rs747849788 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469292 | CTATAAGCCTGGTTT[A/T]CCCAAATTATAGATT | 10580 |
rs747891950 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379556 | CTCTAGGGCAACCTC[A/T]CCTGCTAACCATGCA | 10580 |
rs747893052 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95546776 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTAGAGTGC | 10580 |
rs747898616 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399381 | TGCCAATTCCTTTAC[A/G]TATTATTTATGGGTG | 10580 |
rs747908179 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440787 | ACCCAGATTAAGAAA[C/T]GCCATGAAGGTGTAA | 10580 |
rs747914270 | snp | A/G/T | 3.8913e-05 | 0.00441081 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337233 | ATCTCGGGGGACAGG[A/G/T]CTCGGCGGGAGTGGG | 10580 |
rs747920726 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318675 | GATCACTCTTATTTC[A/G]CTTCATTTGGTTACC | 10580 |
rs747927901 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95400754 | CCAAAGTGATGCAAA[A/G]TAATCCGAGGGACAG | 10580 |
rs747939467 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377814 | TTTTACAAAGACTAT[C/T]TATAAACTGCCCTCT | 10580 |
rs747944509 | in-del | -/ACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376344 | CACACTGCTGCCTAC[-/ACA]ACAAGTCTGAATCTG | 10580 |
rs747950607 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322045 | TGATTAAAGATGATT[C/T]ATTGTCAGAAGGGGA | 10580 |
rs747990453 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537906 | GACGGATCACTTGAA[A/C]TCAGGAGTTCGAGAC | 10580 |
rs748011754 | snp | A/G | 0.00237175 | 0.0343548 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422180 | GGTGAGAATGCAAGA[A/G]AAGCCATACCTGCTG | 10580 |
rs748016570 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467721 | GTATTCTAATTGAGC[A/G]TTAAAAGCCGCCCCA | 10580 |
rs748035339 | snp | C/G | 1.65509e-05 | 0.00287666 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322712 | TAAAAATTCTCTTTA[C/G]AAAAGCTGCAGTCTT | 10580 |
rs748053338 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417457 | ATAGGCACATGCCAC[C/G]ATGCCTGGCTAATTT | 10580 |
rs748070796 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499698 | AGGAAGACCACAACA[G/T]TTTTGTGAGTGCGGA | 10580 |
rs748097563 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499159 | GGCTCACTGCAACCT[C/T]CACCTCCTGGGTTCA | 10580 |
rs748110738 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470730 | CCAAACAACAAGCAA[C/T]AGAATCTGGGGAAAG | 10580 |
rs748117926 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95478114 | AAGAAGAAAACAAAG[C/T]GTATGATAACAGACC | 10580 |
rs748121167 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376175 | ACAGGAGCTGCATTC[A/C]ACAGCAGCAATCATC | 10580 |
rs748121266 | in-del | -/GT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376993 | TTCATGGAATAACAC[-/GT]GTTTCTGGAAATAAC | 10580 |
rs748122348 | snp | A/T | 3.55853e-05 | 0.00421798 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377386 | TTGTAGAAAAATGGC[A/T]GCTAACTTTCTTAGT | 10580 |
rs748128066 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396705 | GGGTTTCTCCACATT[C/G]GTCAGGCTGGTCTCG | 10580 |
rs748163492 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525301 | GACAGCATCTGGTTC[A/C]CAGAAAAAATGGTAA | 10580 |
rs748178727 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552935 | TAAAAAGGAACAAGC[A/G]CAGGCACGGTGGCTC | 10580 |
rs748181125 | snp | A/T | 1.85228e-05 | 0.0030432 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414502 | AGCTTACGGTACTCG[A/T]AACAGCTCCCGTGAG | 10580 |
rs748188793 | snp | A/G/T | 4.94233e-05 | 0.00497087 | missense | SORBS1 | GRCh38.p7 | 10:95410719 | CTAACTGATGGAAAG[A/G/T]CTTGGGAATCAGTTC | 10580 |
rs748201551 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426486 | ACCAGGAGCTCAATC[A/G]ATTACAAAGTTGGAC | 10580 |
rs748210564 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450221 | AGAGCTATGCACCTC[A/G]TATCCCTGTGCTTTA | 10580 |
rs748259151 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502438 | TCTGGGATTTGTGCA[-/G]AATGAAGTAACACCA | 10580 |
rs748263475 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438279 | TTCCTGATACATATA[G/T]ATATTCTATTTCTCC | 10580 |
rs748266168 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395960 | GAGATTGCACTTAGG[C/T]GGGAACACTGACCAG | 10580 |
rs748267186 | snp | C/G | 3.40269e-05 | 0.0041246 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341717 | TTTTAGCAGATGTTT[C/G]AATATGTGTAAGATT | 10580 |
rs748271687 | in-del | -/AG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527126 | TTCAGCTCATATGAA[-/AG]AGAATTTTAACAATT | 10580 |
rs748282700 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518921 | CCATCAGCAGTCTTC[C/T]GTGCAGCCCCACCTC | 10580 |
rs748293304 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355009 | ACAGGCAAAGATTTC[A/G]CTGGAAACCAGCTTG | 10580 |
rs748294872 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313640 | ATATGACAATGCTTT[C/T]TAGGATCCCTCCAGG | 10580 |
rs748311833 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429082 | CACTGTCAGAGTCAA[A/G]AGCCAGCAGGATGTT | 10580 |
rs748312681 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95444072 | GCAATTGTATTAAGG[-/TT]TTTTTATTCCTTATT | 10580 |
rs748337798 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453757 | CTTGGATCAAAAATA[C/T]AGCATTTGTAGGATG | 10580 |
rs748342922 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451116 | GATGCCATCTTCCAC[A/G]GAACTTGTGGGATTC | 10580 |
rs748349082 | snp | A/G/T | 4.95514e-05 | 0.00497732 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434700 | AAATAGAGCGTGCGC[A/G/T]TAAAGGGTCGGCAGT | 10580 |
rs748371615 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373054 | ACTTGCTCTTACATA[C/T]AGAAATCATGTCAAT | 10580 |
rs748381248 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355867 | GGGGCTGACTGGGGA[A/G]GTCTGGCTTCTGGCC | 10580 |
rs748384881 | snp | A/G | 5.79615e-05 | 0.00538306 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414387 | CACACAGGCACAGCG[A/G]CAGCCAGTGCTGTCC | 10580 |
rs748388768 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385516 | TTTCAGAAGAGACAA[C/G]GCCAGAATATTTTAT | 10580 |
rs748391574 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497560 | CTGACCCAAGCCCAC[C/G]CCTCGAACCATATCT | 10580 |
rs748407957 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348805 | TCTTACACAGAACCT[C/G]TGGTCACCCAAGTCC | 10580 |
rs748415249 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524456 | CACTCCCTCCTTTGG[A/G]CCGCCATTGTGCTCT | 10580 |
rs748415662 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467185 | TTAAAGTTTTACTGC[A/G]GAATAATTTATGAGA | 10580 |
rs748419932 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455353 | TCTGAGTAGCAGCAG[A/G]TGTTCTATTCCCACC | 10580 |
rs748424837 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384830 | CTTTCATACACATCA[C/T]TAACAAAGAAGTTCT | 10580 |
rs748427655 | in-del | -/AGTA | 1.65343e-05 | 0.00287521 | frameshift-variant | SORBS1 | GRCh38.p7 | 10:95384238 | TTGAAGTCACTTACT[-/AGTA]GTCTTCAGAAAATGA | 10580 |
rs748437684 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496722 | ATTTTTCCTCCACTA[C/G]GATATGTATTCTTCC | 10580 |
rs748453782 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485391 | TCTTACTGATTATAA[C/T]AGTGAATGCTGAATT | 10580 |
rs748457908 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374322 | TAATTAGGGAAAAAA[A/T]TCCACCATTTTTCCT | 10580 |
rs748473020 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404350 | CCACCAATCACAGAA[C/G]AGCAGTGGCATGAAG | 10580 |
rs748473963 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437456 | TTAGAAATGCCTTCC[A/G]GTACCAATCCAGATT | 10580 |
rs748476476 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361046 | CTCAAACTCCTATCC[C/T]CAGGTGATCCACCCA | 10580 |
rs748495339 | snp | C/G/T | 8.37618e-05 | 0.00647107 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318283 | CTGTTATTCCCTCAA[C/G/T]ACACAACTAGTAAGA | 10580 |
rs748500257 | snp | A/G | 0.00418283 | 0.0455403 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95416041 | GCTGGGGTTGTGAGG[A/G]GTTCTGCTGTCTGGG | 10580 |
rs748505382 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443284 | CAACATGGTGAAACC[C/T]TGTCTCTACTAAAAT | 10580 |
rs748519140 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543797 | TAACAGATAGTGGGG[-/C]CCCTCTGTAGGCCAG | 10580 |
rs748524731 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371108 | TATATTTGAAGAATC[C/T]CCTTTAAGGAAGATG | 10580 |
rs748532261 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435580 | TGTGAGGCCTCCCCT[C/T]GTCCTCTCTTTCAAG | 10580 |
rs748536989 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460712 | GCAAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs748571721 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351911 | CAGGTCATTTTTGTG[C/T]TTCCTGTATCTCTTA | 10580 |
rs748610398 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333239 | GCTGCTACCTGTGAG[C/T]TTTCATCTAAATAAC | 10580 |
rs748625812 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555274 | GGAACCAGTCCTGGT[C/G]GGGGGTGCAGGGGGG | 10580 |
rs748627777 | snp | C/T | 0.000133717 | 0.0081756 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355704 | TATGGCACGGAGTTT[C/T]CATTATTAATGGCCC | 10580 |
rs748632702 | snp | A/G | 1.80286e-05 | 0.00300233 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354983 | CTTTAAAACAACAAA[A/G]TAGAGTTAAAACAGG | 10580 |
rs748650943 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392502 | GTCTAATCATCTTTG[C/T]TATTAATTTTTTTAT | 10580 |
rs748670405 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497659 | CTAAACCTTTGCTCA[G/T]GTCTCTACTGCTTAA | 10580 |
rs748672846 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | SORBS1 | GRCh38.p7 | 10:95399106 | CATCCTTTGCTCTTT[C/T]TTCAATAGCCTTGCC | 10580 |
rs748678673 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472525 | AGGCAGAGATAAGAA[C/T]AGCTTAGGATTCATG | 10580 |
rs748681506 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324929 | GCTGCTGTGGACTAT[A/G]ACTAACTGGGATATT | 10580 |
rs748683299 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502520 | TTCCCCCATCACTCA[C/T]CTTCCAGAGTGTGCT | 10580 |
rs748687447 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436977 | GACCTCAAAGGTCAT[C/T]GCATCCATCATTCAT | 10580 |
rs748691972 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329568 | TAAGTACCGCAGCCA[A/G]CGTCTCTCCCCATCC | 10580 |
rs748703839 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405182 | CAGTAGCTGGTGCCT[A/G]TAATCCCAGAACTTT | 10580 |
rs748710621 | snp | A/G | 1.65018e-05 | 0.00287239 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434690 | TTAACAGCAGAAATA[A/G]AGCGTGCGCGTAAAG | 10580 |
rs748735008 | snp | A/G | 1.65455e-05 | 0.00287619 | missense | SORBS1 | GRCh38.p7 | 10:95315078 | AGATACAAAGGTTTT[A/G]CATAGTTGCCTGGAA | 10580 |
rs748747569 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389837 | TTGCTAGGCGGAGAT[A/C]TCCTGGGAAGCTCTC | 10580 |
rs748787773 | in-del | -/CCCC | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442516 | TAAAAGTATGTGGCA[-/CCCC]CCCCCCGCACCCTTA | 10580 |
rs748810274 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545685 | GAAACTCCATCTTGA[-/AA]AAAAAAAAAAAGGGA | 10580 |
rs748814552 | in-del | -/ATTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342887 | TTATTATTATTTTTT[-/ATTA]TTTTTTTTTTTGAGA | 10580 |
rs748837508 | snp | A/G | 7.90952e-05 | 0.00628819 | stop-gained, intron-variant | SORBS1 | GRCh38.p7 | 10:95337237 | CGGGGGACAGGGCTC[A/G]GCGGGAGTGGGGCAG | 10580 |
rs748837857 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545684 | TGAAACTCCATCTTG[-/AAA]AAAAAAAAAAAGGGA | 10580 |
rs748853033 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514243 | CACATTCAACTAGCC[A/T]TATGAGTCATCTTCT | 10580 |
rs748859915 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502367 | GGGTATGAAGTAAAT[A/G]AGCACTGAATCTGAG | 10580 |
rs748884981 | snp | C/T | 0.000118387 | 0.00769281 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95422190 | CAAGAGAAGCCATAC[C/T]TGCTGAAGAAGGCTC | 10580 |
rs748898304 | snp | A/T | 0.000106491 | 0.00729616 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339358 | AAGAGAGGGTCCTTG[A/T]CCTAGCATGCCTCTG | 10580 |
rs748913403 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542058 | CTTCTGCCTCCAACC[C/T]CAGCCTGGCATTCAT | 10580 |
rs748933693 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421846 | GAGTTGTCCAAAAGC[C/T]TGAAACCTATTCCGT | 10580 |
rs748951040 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351709 | GAGCCAGGGGGCACA[G/T]CCAGGGCATTCCCAA | 10580 |
rs748951187 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504745 | GTTATTATCATATAA[C/T]TTTTCTGGAAAAAGT | 10580 |
rs748953347 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397191 | TTGGCACATAGCACA[A/G]CACAGCTTCTACAAA | 10580 |
rs748964826 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531533 | ACATTCAGCTCATTT[G/T]GAACTCTTTTGACAC | 10580 |
rs748996258 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450578 | ACGATCTCTGCTCAC[C/T]GCAACCTCTGCCTCC | 10580 |
rs748998513 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462077 | TAGACAGGCTTTGAT[A/C]TCTAATAGTCCATTA | 10580 |
rs749005978 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380363 | ATGAATGGTAATACT[G/T]CCAAAACAAAAACAC | 10580 |
rs749019916 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95368369 | GCAAAAGGAAGAAAA[C/T]AACCAAGAGCTACAT | 10580 |
rs749027715 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356099 | TGAGGCCGGGCAGGT[A/G]CCCTTGCACTTGTTG | 10580 |
rs749038934 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397932 | CCCAAAGTCACAGAG[C/G/T]TGATGAGAAGGTGAG | 10580 |
rs749044324 | snp | C/T | 2.34833e-05 | 0.00342653 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422187 | ATGCAAGAGAAGCCA[C/T]ACCTGCTGAAGAAGG | 10580 |
rs749047707 | snp | C/T | 6.61179e-05 | 0.00574931 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410784 | ACTGGAATCCTGAAA[C/T]GAACAAACAAACAAT | 10580 |
rs749051487 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559933 | CCACTTTTAATCCAA[C/T]CCTCCTCTCTTCGAT | 10580 |
rs749061633 | snp | C/T | 4.37598e-05 | 0.00467739 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336500 | GACGCCAAGTGCACA[C/T]GCGGCATGCTGCAGT | 10580 |
rs749069181 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411337 | ATTTGGAGATTATCC[C/T]ATCCTACTGTGACAT | 10580 |
rs749083803 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327168 | AATAAAGTTAAGACT[A/G]AAAAAAAAATGCTAA | 10580 |
rs749103362 | snp | C/T | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561812 | CCATCTGTAAAATGG[C/T]ATAATAGTCCGACTT | 10580 |
rs749114264 | snp | A/G | 1.70525e-05 | 0.00291992 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357587 | GCTCAGTGAATGGAG[A/G]TGGATGGGAGACAGA | 10580 |
rs749122302 | in-del | -/T/TTTTTTTTTTTTTTTTTTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347441 | TCTATCTGGAATTTC[-/T/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 10580 |
rs749146120 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489547 | CCCACTCAAATCTAA[G/T]ATCCAGGGAGGCATA | 10580 |
rs749150669 | snp | C/T | 1.6504e-05 | 0.00287258 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322734 | TGCAGTCTTATTCAA[C/T]AGGCATCTTACCACA | 10580 |
rs749154685 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549178 | CTGCCCATGCCGACC[A/G]TAGGGCAGTCACTAG | 10580 |
rs749172657 | snp | C/T | 1.91463e-05 | 0.00309399 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414417 | CTCAGAGCTCAGTGC[C/T]TCAGTGAGAAAGGGA | 10580 |
rs749176127 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520492 | AAAAATTAGCCGGGC[A/G]TGGTGGCGCACGCCT | 10580 |
rs749178204 | snp | C/T | 3.53101e-05 | 0.00420164 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339124 | ACCAGTGACGAGAAG[C/T]TTAGATACCTGTGGG | 10580 |
rs749180046 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428796 | GCAGAGCAGCTGGGG[G/T]ACAAATGCTGTCCCT | 10580 |
rs749184521 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316939 | TTGCATTTCTATTGG[A/G]TTGCACTGCACCAGA | 10580 |
rs749197543 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377780 | ATGGGGTTTCATGAA[C/T]CTATTTCATGTTTGT | 10580 |
rs749198972 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492389 | AAATATTTATTGAGC[C/T]CTATTACACTCCAGG | 10580 |
rs749204078 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358122 | GGGTTGGAGGAAGGA[C/T]AGGGGAGAACAGGGG | 10580 |
rs749205238 | snp | C/G | 1.67987e-05 | 0.00289811 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381824 | GAAAATTCTATTAGA[C/G]CTATTTTCATGACAA | 10580 |
rs749213509 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510214 | GATATGAAAGTATTT[C/T]CTTTTCTCTTTTTAT | 10580 |
rs749214136 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386607 | TGCCCCTGTACTCCA[A/G]CCTGGCTGATGGAGT | 10580 |
rs749220986 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347236 | CATTCTTCCTCACAT[A/C]TCTTCCTTGCTTTGA | 10580 |
rs749227382 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509052 | TCAGATAACAGTCCA[C/T]GTTCCTGAGATTGGA | 10580 |
rs749245207 | snp | A/G | 6.0241e-05 | 0.00548788 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422253 | TGAAAACAAGAAAAG[A/G]GGAAAAACAGAAATG | 10580 |
rs749246420 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498263 | AAGATAAAAGGCCCA[A/G]TCAGACACGAATGGT | 10580 |
rs749271357 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385650 | TGTCTCAGGTCTCCC[C/T]TGGCCCACATAAGGG | 10580 |
rs749301807 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324717 | GTCCGTATCACAAAG[C/G]AAAGAAATGGACATT | 10580 |
rs749311881 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549174 | ACAACTGCCCATGCC[A/G]ACCGTAGGGCAGTCA | 10580 |
rs749312193 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489306 | TTCAAAAAGAGCCCC[A/G]CCAGCCCTTCACCTT | 10580 |
rs749315871 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418854 | AAGGACCACTTGAGT[C/G]TGAGACCAGCCTGGG | 10580 |
rs749340639 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446977 | GAAACCCCATCTCTA[A/C]TAAAAATACAAAAAT | 10580 |
rs749367698 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497419 | TCAGACCTGGGTATT[A/T]CCCAGGAAACCCAGT | 10580 |
rs749367928 | snp | G/T | 3.30437e-05 | 0.00406457 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394566 | AAGGTAAAAAAGAAA[G/T]TAGCAGCACCAGTAC | 10580 |
rs749368472 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387981 | TTGCTACATCTTTTC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs749394712 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448549 | AACACAGGCCTGATG[A/T]TACAGCTCAAAAACA | 10580 |
rs749397840 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406832 | TCCCTGACTCCTAGT[A/C]CAGAGTTCATTCCAA | 10580 |
rs749438464 | in-del | -/A | 3.40373e-05 | 0.00412523 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354866 | AAAACTAATGGATTT[-/A]AAAGATGGGATTTAC | 10580 |
rs749439661 | snp | C/G | 1.66222e-05 | 0.00288285 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346365 | GCTGTGTTTCAAAAA[C/G]GCAGCTAAAAAGACA | 10580 |
rs749444864 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323060 | GCAGTGAGGTGAGGA[A/T]GAACAACACAGGGTC | 10580 |
rs749446409 | snp | G/T | 1.67843e-05 | 0.00289687 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375922 | AGCAGCAACAACGCA[G/T]CCACAGCATTAGTTT | 10580 |
rs749450281 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313315 | TGATGGGATCCTAAG[A/G]TGGGTATTTGTGACA | 10580 |
rs749451328 | snp | C/T | 3.29826e-05 | 0.00406082 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441111 | TAAGAGAAAGATGAG[C/T]TTAAAATGACTTACC | 10580 |
rs749476706 | snp | C/G | 5.3968e-05 | 0.00519433 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337075 | TGAGAGACAGGGAGG[C/G]ACTGGCCCTTGGTGA | 10580 |
rs749481700 | snp | A/G | 5.01727e-05 | 0.00500838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318293 | CTCAATACACAACTA[A/G]TAAGAAAAGCATGAT | 10580 |
rs749492111 | snp | A/G | 3.46897e-05 | 0.00416457 | intron-variant | SORBS1 | GRCh38.p7 | 10:95354834 | ATCTGTACTTGCTTC[A/G]TACATTTTTCCAAGC | 10580 |
rs749492331 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353903 | TCCTAAATCCTTCGG[A/G]AAACCCCACCTAAAC | 10580 |
rs749498984 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505278 | CCTCCCACGTTCTGC[G/T]GGACTCCGTGGGAGT | 10580 |
rs749506452 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530330 | TTATCACACAGCTTT[A/G]TAATCATCTTGTTTA | 10580 |
rs749515464 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396594 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 10580 |
rs749536318 | snp | C/T | 1.65474e-05 | 0.00287636 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371994 | ATTACCTTTCTATCC[C/T]CTCTAGGAAGGATAG | 10580 |
rs749541384 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424460 | ATCAAATATTGGGGG[-/A]AAAAACACAAAATAA | 10580 |
rs749549238 | snp | C/T | 1.65756e-05 | 0.00287881 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394661 | TGGTAGGTGGGAGTG[C/T]AAGGATTGTCCTCTG | 10580 |
rs749567424 | in-del | -/ACAGGGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461848 | TGCACACAGTCTGGC[-/ACAGGGT]ACAGGGTTTCCGAGT | 10580 |
rs749592063 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95437518 | ATTGCTGCCAGGTGC[C/T]AAGCCATTCATCACA | 10580 |
rs749592088 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436938 | CCACACTGAGGTCAG[A/G]ATGAAAGTCTCCAGG | 10580 |
rs749599212 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495482 | AAGTTCTCAAAGCCC[C/G]ATGTATCTCTCCTTC | 10580 |
rs749603569 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384677 | ACCAGCTCAGTGTAC[A/G]GTTAAGCTCACCGAG | 10580 |
rs749605637 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369019 | TGCAGGCTCCAGATT[A/C]TTTGCCATATACTCT | 10580 |
rs749621878 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95318387 | GCGGAGTTCCAACTC[A/G]TCATCATTCTGTGGT | 10580 |
rs749667790 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462852 | TATCATCAAGAGCCT[-/C]CCCCTCATGCTTAGC | 10580 |
rs749687563 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413570 | TCTCTATGTCAAGCT[C/T]CATAACAGGAACTTT | 10580 |
rs749699846 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483561 | TTGCTCTTGCTGCCC[-/A]AGGCTGGAGTGCAAT | 10580 |
rs749701885 | snp | G/T | 1.66186e-05 | 0.00288254 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376065 | CCCGACTCTATAGGG[G/T]TTGGTGATAGAGAAA | 10580 |
rs749706833 | snp | C/T | 1.67835e-05 | 0.0028968 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336579 | CCACCTCTATGCCGC[C/T]CTGTCTGCTCAGCCT | 10580 |
rs749710229 | snp | C/T | 0.000673446 | 0.0183377 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355719 | CCATTATTAATGGCC[C/T]TTGGGTAGTCCTCCA | 10580 |
rs749744780 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524305 | GAGATGCCAAAGATA[C/T]CATGCACCTAGATTT | 10580 |
rs749745842 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484366 | TGATGTGGGGACCAC[A/T]GCAAATTGGACTCCC | 10580 |
rs749759779 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332111 | CCTCTCTCACTGAGT[C/G]CCCTGCTGCACCCTT | 10580 |
rs749763061 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346600 | AATTGCATTTGTCTG[A/T]CCTTAGTAGAACACT | 10580 |
rs749775632 | in-del | -/TC | 1.67066e-05 | 0.00289016 | intron-variant | SORBS1 | GRCh38.p7 | 10:95375945 | TTAGTTTAAAAGGTG[-/TC]TATAACCACTGAAGC | 10580 |
rs749785159 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495177 | GGCATGAGCCACCGC[A/T]CCCGGTGGTGGTCCT | 10580 |
rs749793491 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435234 | GCCTGCTCCGATAAT[C/T]GTAGCCCTCTGGCCC | 10580 |
rs749794852 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95372993 | CAAATTTCATTATAG[C/G]CAACTCCATGGAAGC | 10580 |
rs749799925 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513072 | TCCGAAATAAACAAA[C/T]TCTCTTGTATAAGGT | 10580 |
rs749801396 | snp | C/G | 1.64806e-05 | 0.00287054 | missense | SORBS1 | GRCh38.p7 | 10:95384081 | ATGTAGCTCATCTCA[C/G]TTTTTGAGCGAGGCA | 10580 |
rs749802692 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496429 | AGGTCGCTCCCACTT[C/T]CCAAACACCTCTTGG | 10580 |
rs749803187 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434162 | TCTGGGATGGCCCGG[-/T]GAGCATCAGAGGCGA | 10580 |
rs749803244 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472074 | GTCGACTAAAACAGG[A/G]TGAGGACACTTTGCA | 10580 |
rs749808836 | snp | A/C/T | 3.31638e-05 | 0.00407198 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406182 | AGTGTAAGTAAGATT[A/C/T]ATACAGCACATAGTA | 10580 |
rs749814757 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516092 | GGTCAGTGGGTTTTA[C/T]CTGTCACTGTCTAGG | 10580 |
rs749827992 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459272 | CTCTCAGAATGGTAA[C/T]GAAGCATTTCAAATT | 10580 |
rs749831146 | snp | C/T | 1.72502e-05 | 0.0029368 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399235 | CTCTTTTGGTAGCTG[C/T]AAAACAAAACGCTCC | 10580 |
rs749832913 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385251 | CTAGTCACTACATCC[A/G]TGATGGTCCCTCCAA | 10580 |
rs749845202 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496256 | AATCACACTGCATTA[G/T]TTTATTTAAGATGAA | 10580 |
rs749846357 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485130 | AGGCTGCCTTGAACA[C/T]AGCTATCTTCCCCAG | 10580 |
rs749849984 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403068 | TGAGGATTACAGCAA[C/T]GCTCACACTTCTCTG | 10580 |
rs749892209 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344975 | TAAAAAAAAATTGTT[G/T]TAAGACTCTTTATGA | 10580 |
rs749911047 | snp | A/T | 1.64879e-05 | 0.00287118 | intron-variant | SORBS1 | GRCh38.p7 | 10:95441078 | GGGAAATCTGGGTAA[A/T]CTGCCCAGTTTGGTA | 10580 |
rs749921655 | snp | A/G | 1.65493e-05 | 0.00287652 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95376031 | TCATTCTTTAAATCT[A/G]TCTCTTCTGGGCTTA | 10580 |
rs749924305 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426977 | AATTTAATGGAGGTA[C/T]GGGGTACCTTCAACT | 10580 |
rs749944745 | snp | C/T | 1.79942e-05 | 0.00299946 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337046 | ACGATCTGACCAACT[C/T]AAATGGGGGAGGCTG | 10580 |
rs749945183 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414328 | CCCAGGGAAGACACA[C/T]GGGAAGCATGCACGC | 10580 |
rs749946435 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319341 | CTATCCCAGTGAGCA[C/T]TGAGGGCAAGATTTT | 10580 |
rs749947508 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332064 | AAGGTCCATAAATGC[C/T]CCTAAGGAAAATCCA | 10580 |
rs749948523 | snp | A/T | 1.67147e-05 | 0.00289086 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315177 | ACCCACTCGCTTGAG[A/T]TGAGACAGCACGCTG | 10580 |
rs749949701 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321906 | GCCAGCGACCCACTT[C/T]CTAAGACCAACAGTC | 10580 |
rs749963605 | snp | A/G | 1.66732e-05 | 0.00288727 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372074 | AGCAGAGGAGGAAAT[A/G]AAGAAATGAGCATAA | 10580 |
rs749967790 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95372301 | CAAGAGCAAATCATC[-/T]GTTGGATTCTAAATA | 10580 |
rs749971152 | snp | A/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315010 | AAGATCGGTTCATGA[A/T]TGATGCTTCCTCCTC | 10580 |
rs749974373 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455868 | TTGAGCCTGGGTGGT[C/T]GAGGCTGCAGTGAGC | 10580 |
rs749979347 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427958 | CTTTGACCTCAGCCT[C/T]TGCTCTTCACTCCCA | 10580 |
rs749984258 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321436 | AAATACCACCCACTC[C/T]ATGCCTTTGCACATG | 10580 |
rs749998897 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345215 | TTACCCCAGCTTCCC[C/T]GCAAGAGAGGCATTT | 10580 |
rs750001054 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491991 | AGGACTCGTACACTA[C/T]GCTGGACTACATACT | 10580 |
rs750029538 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457018 | TGGATGACAAGATAA[A/G]ATTATCAGAAAATAA | 10580 |
rs750037378 | snp | C/G | 1.68009e-05 | 0.00289831 | intron-variant | SORBS1 | GRCh38.p7 | 10:95421947 | CCCCACCCTGCCCTT[C/G]GGCACATGCCTACCT | 10580 |
rs750040703 | in-del | -/TCAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491568 | TATGTCTTAAAATGA[-/TCAG]GTGGTGCTAAGCATT | 10580 |
rs750046241 | snp | C/G | | | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415628 | AACGGCATCTTTACG[C/G]ATGTCAAAGAATAGC | 10580 |
rs750049167 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362092 | GAATTCAGCCTCTGG[C/G]TAAGATGCAGAGCTG | 10580 |
rs750058938 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525052 | GAAGAAGAGCTAATG[C/T]TATAGATGCCAGAAT | 10580 |
rs750059067 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537133 | CCAGTCTGTAACGCC[A/C]CCTTATCCATCTAGG | 10580 |
rs750060715 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525105 | GCCCAGCATTCTGGG[C/T]GAAAAACAAAGCCGA | 10580 |
rs750061467 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321108 | CACGGTTACAAAATG[C/T]CCACTTTGTCCTGGC | 10580 |
rs750061826 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373722 | TGCCACTTTTATTTA[C/T]GTCTCTTACTCTTTT | 10580 |
rs750062689 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374961 | TGCCAAATCAAAGAG[C/T]AATTCCTAAGCACCA | 10580 |
rs750066098 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356179 | TGCTGTCAGTGGAGA[C/T]ATTTGAACAGCGGTC | 10580 |
rs750066862 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380989 | CAATGAAGGGTTAAT[-/A]AAAAGGATGCATGAT | 10580 |
rs750078864 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547815 | TCCCATCCCTGGGGC[A/T]AACATCAGAGCTCTC | 10580 |
rs750098176 | in-del | -/GA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449339 | CCCCTGGGTTCAAGT[-/GA]GATTCTCGTGCCTCA | 10580 |
rs750103553 | snp | C/T | 0.00111379 | 0.0235723 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415735 | CTCGGGTGCCCGCAG[C/T]CTCCAAGGGAGTGCC | 10580 |
rs750127566 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467072 | TATTTTCTTCAATGA[C/G]TTCTGGGGTAGAAAA | 10580 |
rs750149427 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417624 | TCTTTAATGGCTCCT[-/TT]TTTTTTTTTTTTTTG | 10580 |
rs750153413 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419484 | CTTTTACTTTCAGCT[A/C]AAATGTCCCATATGT | 10580 |
rs750178442 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554196 | AACTGGGATTACAGG[C/T]GCCCGCCACCGTGAC | 10580 |
rs750184778 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389723 | AGAAGAAGACTCACC[A/G]TCTTCATCTGCTATC | 10580 |
rs750216131 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432939 | AAGGCACAGTTCAAG[A/G]AAGAGTTTATGAAAG | 10580 |
rs750218691 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433894 | CAAACTATTGGGAAA[A/C]CTGGTTCATAGTCAC | 10580 |
rs750221851 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445484 | TCTGAGTGCAGTTCT[C/T]CAACCTTCCATAAAC | 10580 |
rs750226877 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541883 | CCTCCCATGACCCCC[A/G]CAGTGCTCTCTGACT | 10580 |
rs750231047 | snp | A/T | 3.30732e-05 | 0.00406638 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406154 | TTTGCTGTTCTGTGA[A/T]AAAAGAACACACAGT | 10580 |
rs750235251 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461962 | ACCCTACCTTTAAGA[A/C]TATTTCATATCATAA | 10580 |
rs750236972 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476876 | TTAATAATGGAATTA[A/C]GGTGCTTTTCTTAAG | 10580 |
rs750244224 | snp | C/T | 1.72311e-05 | 0.00293518 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95339322 | GAGCAGTGTGATCCT[C/T]TCACCCTGGAAGACA | 10580 |
rs750261179 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322251 | TGTAACATTCCAGAC[A/G]AAGCACATAAGTCCA | 10580 |
rs750265946 | snp | C/T | 8.23974e-05 | 0.00641809 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384038 | GAGGGGTAGTGTGGC[C/T]GACCTCTTGACTACC | 10580 |
rs750272308 | in-del | -/CAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383415 | AGCAAAACTCCGTCT[-/CAAA]AAAAAAAAAAAAAAA | 10580 |
rs750279848 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531228 | CTTGCCGGAGGTCAC[A/G]CAGCTCAAAAGCAGC | 10580 |
rs750295325 | in-del | -/GGGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509002 | TTTGGAGGTGACTGG[-/GGGT]GGCCCTGGGAACAAA | 10580 |
rs750304282 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95368146 | CCTTCATGCACCCCA[A/T]ATGCCACATCCAGAG | 10580 |
rs750305003 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455304 | AATAGCATCTGGGGC[A/G]GGGGTCAGAACCACT | 10580 |
rs750306950 | snp | G/T | 2.13837e-05 | 0.00326977 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357854 | GGGAAAAAATAAAGA[G/T]AAGAATAGGAGTTAG | 10580 |
rs750322858 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503462 | CAGTAAATAGAGAGG[A/G]GTATTTCCCAGGTCT | 10580 |
rs750340266 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543305 | TCAGGAGGCTGAGCC[A/G]GGAGAATCACTTGAA | 10580 |
rs750357655 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393585 | GGCCCACTGTGTGCC[C/G]GCAAGGTTTTCTGTG | 10580 |
rs750359232 | snp | G/T | 1.68462e-05 | 0.00290221 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432626 | CCAAGACTCCTGAAG[G/T]ATTAAAGGACAGTTG | 10580 |
rs750360394 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382413 | CATAATTGCATTCTT[A/C]CCTGTTCCACACTGG | 10580 |
rs750383547 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532881 | TGTTAATCCATCACA[C/T]TGACTTCTGATTAAC | 10580 |
rs750389603 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533978 | AGGCTGTCTAGAAAT[C/T]ATTGTTTTTGAAATG | 10580 |
rs750392152 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450987 | CCTTTTTAGCTCCTA[C/T]GTGACATTTGATATG | 10580 |
rs750406658 | in-del | -/C/GGC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560086 | CGGGGGGCTGGGCGG[-/C/GGC]GGGGGGGGGTGTTGA | 10580 |
rs750412615 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523769 | AAAGGTTAAGTAGCT[G/T]ACACATCAGGCTCCC | 10580 |
rs750430173 | in-del | -/CTT | 1.65179e-05 | 0.00287379 | cds-indel | SORBS1 | GRCh38.p7 | 10:95315114 | CCAAACTGCTTTGTC[-/CTT]CTTGAAGTACCTATG | 10580 |
rs750443688 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370248 | CTCCATATTCCTTTT[A/G]TATCTTTTTTTTTTT | 10580 |
rs750457219 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511524 | CCAGCCTGTTGATAC[A/G]TCTGTCTCCTAAAGC | 10580 |
rs750459208 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95401971 | CATTCTCCTCCCACC[C/T]GGAAAGGCCTTCTGT | 10580 |
rs750480755 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460569 | ATACAATAATTAGTC[A/G]GGCGTGGTGGTGTGT | 10580 |
rs750494159 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318263 | TTTGCATGGCTCATC[A/G]CCCCCTGTTATTCCC | 10580 |
rs750495403 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560865 | GCAGAGGTGCCCCTC[C/T]TCGGTAGTTTCACTT | 10580 |
rs750496852 | snp | C/G | 1.76061e-05 | 0.00296694 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337149 | GGAGGCAAGGGTGGG[C/G]TCAGGGCCAGAGAAC | 10580 |
rs750543939 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95329879 | TTTCTCTAAGCCTAT[A/G]GTTTGTTCTTATGCT | 10580 |
rs750546451 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471529 | TTGAGACCAGCCTGG[A/G]AAACATAGTGAGACC | 10580 |
rs750553343 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431189 | CCTCCCCTCCATTCC[A/C]TTTCTCCCTCCCTTT | 10580 |
rs750561559 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350131 | TACAGGTGTAAGCCA[C/T]TATGCCCAGTCATAT | 10580 |
rs750564148 | snp | A/T | 8.24504e-05 | 0.00642016 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367735 | AAAAAAAGAAGAAAA[A/T]AATAATGTAGATGAT | 10580 |
rs750565631 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539427 | CCCATGAGAACCATT[A/G]CCAAAGGATGACCTC | 10580 |
rs750569638 | snp | C/T | 5.53919e-05 | 0.0052624 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337217 | AGAGGTGACAGCGTG[C/T]ATCTCGGGGGACAGG | 10580 |
rs750571105 | snp | C/T | 1.67492e-05 | 0.00289384 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414639 | GCGCGGGCTGGCTGG[C/T]TGTGGTGGGGCCACC | 10580 |
rs750586850 | snp | A/C/G | 3.29496e-05 | 0.00405881 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351306 | GTCGGAATGACGCCT[A/C/G]TGTGGCGTCGAGCTG | 10580 |
rs750603876 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | SORBS1 | GRCh38.p7 | 10:95397250 | GGATCTGTTTAAACA[C/T]AGTCTTGTACCAGTC | 10580 |
rs750604478 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512631 | GTTAGATGCTCCCCT[A/G]AAATCAGCCCACCTG | 10580 |
rs750609491 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335956 | TATTCGAGGATACCC[C/T]ATGTCAGTCAGGGCC | 10580 |
rs750618439 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528644 | CTGTTTCTGGCTGGG[C/T]GCAGTGGCTCACGCC | 10580 |
rs750619138 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378493 | ATTCCTAGTCCAGTG[C/T]TCTTTACACTATACC | 10580 |
rs750631638 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499528 | CTGCCCTGTAAATGG[C/G]CAAGGCTCTCCGATT | 10580 |
rs750655109 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436734 | AAATAAATACGGCAG[A/T]TCATAAATTCCCTCA | 10580 |
rs750673719 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95388969 | AGACAACTGAAGAAA[C/G/T]TAGTTGTTGAAAGTT | 10580 |
rs750673961 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373182 | TGTTCACCACTGACA[A/G]CAACAGGTCAGTAAT | 10580 |
rs750675464 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360139 | CCTATTCATTATCCA[C/T]CCTCTTCCCTTTGGT | 10580 |
rs750678895 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459554 | CAGGCGGGCTCCGGA[A/G]TGTGCCCTAGACACT | 10580 |
rs750682175 | in-del | -/ATCTA | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312994 | ACAGTGCTCTTAGAT[-/ATCTA]GGTGGAGCAGACCTT | 10580 |
rs750686209 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500579 | CATATGGAAATGATA[A/G]TATTTTGGATATACT | 10580 |
rs750695893 | snp | A/G | 3.29696e-05 | 0.00406001 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414723 | GCGGCAGAGGCAGTC[A/G]CTGGGATTGTGGGGA | 10580 |
rs750709779 | in-del | -/AAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528929 | GTCTCAAAAAAAAAA[-/AAAAA]AAAAAAAAAAAAAAA | 10580 |
rs750730173 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447988 | TTTCCGTTCTAACCA[A/G]TTATCTGAAATGGCC | 10580 |
rs750741187 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489964 | ACCAGGTAGTGTTAA[A/T]CAGGCCAGCTTTTCT | 10580 |
rs750750545 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419891 | TAGTTTATACAGTTC[C/T]ATAAACTACCAATTC | 10580 |
rs750754230 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421143 | TTGCACTCTGGCCTG[A/G]GCAACAGATAGAGAC | 10580 |
rs750756033 | snp | G/T | 5.33889e-05 | 0.00516639 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422110 | ATCTCTCACTCACAG[G/T]GAATAACTCCCTGGT | 10580 |
rs750759817 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416783 | GCATAACAAATTAAC[A/G]TGCCCTAAGAAGAGA | 10580 |
rs750765509 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409061 | CAAGGAAGAAACAAA[A/G]AGGAACTACAGGCAT | 10580 |
rs750770024 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325853 | AGCCACTGTGCCCGA[C/T]CCCACTTCTATACTC | 10580 |
rs750812119 | snp | A/G | 4.94539e-05 | 0.00497238 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95322790 | CTGGTCCTGCTCTCA[A/G]TGAATGATGAGAAAG | 10580 |
rs750815094 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436756 | ATTCCCTCATCTTAT[A/G]GATAAGGGAACCCAC | 10580 |
rs750850654 | snp | C/T | 0.000120985 | 0.00777675 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356926 | GTTCCTGCAAAAGAG[C/T]GCTGGGAGCAGAGAG | 10580 |
rs750852791 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559587 | TGAGAAATGTGCTCT[C/G]TGCAACCCCTGGAGA | 10580 |
rs750854057 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381004 | TAAAAGGATGCATGA[C/T]TGGCAGGTATGAAAC | 10580 |
rs750854147 | snp | C/T | 1.66366e-05 | 0.0028841 | missense | SORBS1 | GRCh38.p7 | 10:95381693 | ACATTACCATCTTTT[C/T]GTTGGTCAGAACGGA | 10580 |
rs750854344 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529565 | CAGGCCCAGCCCCTA[A/G]AAAGGTTAACTGTAT | 10580 |
rs750885641 | snp | A/C | 3.37223e-05 | 0.00410609 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410818 | ACTAACTGTAAATAT[A/C]AAAAGCTAGTGTTAA | 10580 |
rs750905628 | snp | A/C | 0.000101877 | 0.0071364 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95422216 | GGCTCTGGCTCCAGA[A/C]CTACACGTGGTGCAG | 10580 |
rs750926900 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518384 | AGACCTTGGAGACTC[A/C]ATGCAACATGATATA | 10580 |
rs750945677 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535148 | CAGCAAATCAGGGAA[A/G]GCTTCATGAGGGCTA | 10580 |
rs750946802 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95558669 | CTCTCACTCTGGACC[A/G]TTCTAGCTCTGAATT | 10580 |
rs750949838 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506903 | TCTCCCTCTGTCGCC[C/T]AGGCTGGAGTGCAAT | 10580 |
rs750950306 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95410688 | CGTTGTGGAGGGATA[A/G]GCGGATGAAGGCTTG | 10580 |
rs750973913 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396268 | GCTTTGGTGTGTCAG[A/C]TCCTGACTGACTCTC | 10580 |
rs750995990 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477464 | CTGGGAGCCCAGAAA[A/G]CCAGTCACAGCTTAA | 10580 |
rs750998796 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465313 | GAGGGCGGATCACGA[A/G]GTCAGGAGATCGAGA | 10580 |
rs751002146 | snp | C/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313891 | CCTCTCTCTTCTGAT[C/G]TGGCCCCCACAAAGA | 10580 |
rs751004328 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340353 | TACAACCACCTAGGA[C/G]AGAGCCATCTATCTT | 10580 |
rs751007296 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95396424 | TTCTCCGGAGGAAAG[A/G]AAGCAGAACAAACAC | 10580 |
rs751049392 | snp | A/G | 1.65288e-05 | 0.00287474 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321919 | TTTCTAAGACCAACA[A/G]TCCTCTGAGAACATG | 10580 |
rs751090877 | snp | C/G | 3.52144e-05 | 0.00419594 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339347 | AAGACACAGCAAAGA[C/G]AGGGTCCTTGTCCTA | 10580 |
rs751100350 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95319286 | GCTTTTAAATGTGGA[-/T]GTCATTTTTCTGAAA | 10580 |
rs751101322 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325458 | ACAAGCATATATAGA[A/T]CCATTACATATCTGA | 10580 |
rs751102098 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312715 | TGAGGCTGGCATCAT[A/G]TGCAAATGTGGCTTT | 10580 |
rs751107864 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95437746 | TCCTCCCTTCTCACC[A/T]GATGGAAATTCCACG | 10580 |
rs751109995 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545988 | CTCAGCCACCAGGTT[C/T]CACACAGACTCCAGG | 10580 |
rs751125183 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330313 | ATGCCAGTCAACAAA[C/T]AGTGCTTCTGTCACA | 10580 |
rs751133001 | in-del | -/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391323 | TATTCAGCACAGAAA[-/GC]CTTGTATGTGGCAAG | 10580 |
rs751138252 | snp | C/T | 1.78458e-05 | 0.00298707 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377303 | TGTGCAGGTCTTTAA[C/T]GCTAGTGCTTCACAA | 10580 |
rs751151986 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510960 | ATGCACATTTATCTC[A/G]TTCCATGCAAGCCTG | 10580 |
rs751158044 | snp | G/T | 4.97996e-05 | 0.00498972 | missense | SORBS1 | GRCh38.p7 | 10:95421965 | CACATGCCTACCTGG[G/T]ACTTGTCAGAAGGAA | 10580 |
rs751176469 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354605 | ACAGGGCATTAAGTG[C/T]AGCAGTGGACAATCT | 10580 |
rs751177610 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535109 | TGGATGAGTAGATGG[A/G]TACAGATGCCCAGGA | 10580 |
rs751190513 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488104 | GAGAAAAATACCTGA[A/C]ATGTAATAACAGTAA | 10580 |
rs751201651 | in-del | -/AAGGGAAGAAGA | 8.23757e-05 | 0.00641725 | cds-indel | SORBS1 | GRCh38.p7 | 10:95410739 | GGAATCAGTTCCAAT[-/AAGGGAAGAAGA]AACTTCATTTAGTAG | 10580 |
rs751220714 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507184 | CGTGTTAGACTCATC[C/T]TTATCAAGACTCAAA | 10580 |
rs751224879 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414179 | CTCACCACACGACCC[C/T]CGACCTGGCCTGTGA | 10580 |
rs751242506 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384299 | ATCTATTGAACAAAA[C/T]AAAATGTAGTCAGGA | 10580 |
rs751251145 | snp | A/C | 8.28713e-05 | 0.00643652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406177 | CACACAGTGTAAGTA[A/C]GATTTATACAGCACA | 10580 |
rs751276936 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513060 | GTGGGCTGATTCTCC[A/G]AAATAAACAAATTCT | 10580 |
rs751280792 | snp | A/T | 1.71962e-05 | 0.0029322 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422087 | ATCTGAGAAATAGAG[A/T]GGAAAAAATCTCTCA | 10580 |
rs751305825 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484928 | GCAATGAGCCATAAT[C/T]GCACCACTGCACTCC | 10580 |
rs751314941 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472729 | CCAAGACCATATATA[A/C]CTCAATAGTAAATGA | 10580 |
rs751319883 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454891 | CTTACCTGGGAAACA[C/T]CCAGGCACATGCTGA | 10580 |
rs751339487 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443838 | GTCACTGTCAAATAC[A/T]TCTGAGACTATCTAT | 10580 |
rs751343159 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443032 | TGTACATACCTCGAC[C/T]AATAAGGTCTTACTG | 10580 |
rs751358101 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350323 | TCCCAGACTTACCCA[C/T]TTTCCCTAAAAGAGA | 10580 |
rs751364606 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530589 | CTCTGCTCAAATCTG[-/A]AAAGTCAAGTCACCT | 10580 |
rs751372301 | snp | A/G | 1.6715e-05 | 0.00289089 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384315 | AAAATGTAGTCAGGA[A/G]AAGTCTGGCTAAGGT | 10580 |
rs751389380 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336804 | CTCTCTTCGCGCCAT[A/G]GCTGCCTCTTGCTCT | 10580 |
rs751412845 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331753 | AAAAACTCCTTATCT[C/G]AGGAATTTAGAAGGG | 10580 |
rs751431618 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379962 | TTCTCTTTGGAGGAA[C/T]AGAGCTAAACTGGGT | 10580 |
rs751432467 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322139 | AATGTTTATGATCTC[A/G]TTGCAAACCGCTTCC | 10580 |
rs751437368 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460713 | CAAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs751448944 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351392 | CTGCCATAAAATTGC[A/G]TAAAATGGGCAGTGA | 10580 |
rs751451057 | snp | A/G | 1.67975e-05 | 0.00289802 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371446 | GTTCAAGAAAGAAAA[A/G]ATGGGAAAGAAGGTT | 10580 |
rs751462248 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356544 | CTGGGGCCCAGCTCA[A/C]CCCTGGACAATGCCA | 10580 |
rs751462546 | snp | A/C | 1.6646e-05 | 0.00288491 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414652 | GGCTGTGGTGGGGCC[A/C]CCTCTGCAGATGAGG | 10580 |
rs751466567 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361709 | ATCCTCCCGCCTTGG[A/C]CTCCCAAAGTGCTGG | 10580 |
rs751505325 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460858 | CCCTAATAAAACCAT[A/C]ATCATCTCTTTTGCA | 10580 |
rs751511067 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414748 | TGGGGACGCAGCCAA[A/G]AGGCCCCAGAGGTGT | 10580 |
rs751529149 | snp | A/C | 6.59402e-05 | 0.00574158 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434643 | GGAGAACTAGGCCTG[A/C]GGCGTTTTTCACTGT | 10580 |
rs751529188 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541824 | CCTTTCCTCCCTCCT[A/G]TTGGTCCTTCAAGGC | 10580 |
rs751559314 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473538 | GAGGCTGAGGCAGGA[C/G]AATCGCTTGAACCTG | 10580 |
rs751575921 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502089 | TAAGCCAAACAGTCA[C/T]TGCTCCTTCCCTTGG | 10580 |
rs751577266 | snp | A/C | 3.51685e-05 | 0.00419321 | intron-variant | SORBS1 | GRCh38.p7 | 10:95337343 | AAGAAGCAAAAGGTA[A/C]AAGTGTCAGCATAAA | 10580 |
rs751581851 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390584 | CCCCATCCCAGTGGT[G/T]CTCAATCCTGTCTGT | 10580 |
rs751592122 | snp | A/C | 3.39064e-05 | 0.00411728 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315039 | TCCAATAAAAATAAT[A/C]TCCATGGTTTTCAGT | 10580 |
rs751630387 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327847 | TGAGAAAATCCAGGT[G/T]CCAGGCCATGCTCTG | 10580 |
rs751635862 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451545 | CAAAACAAAGCTGTC[A/T]AATTGTGGCATTCAG | 10580 |
rs751644007 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328518 | CTCTTCATAGACTAT[C/G]ATACAGTCTTCTCTT | 10580 |
rs751658723 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424581 | ATTTAAAATATACAG[A/G]AGATCTGCATAGGTT | 10580 |
rs751658771 | snp | A/G | 1.87184e-05 | 0.00305922 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337225 | CAGCGTGCATCTCGG[A/G]GGACAGGGCTCGGCG | 10580 |
rs751686010 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316814 | GTTCAAATGGTAGCA[G/T]TTTGAATGCACTGGG | 10580 |
rs751690719 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411989 | TGAGGGGCAGCTCAA[A/T]GTCATGAATAAAACC | 10580 |
rs751691574 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549855 | TTGGGAGAAAACAAT[C/T]CTCTAGTGTCAAGGC | 10580 |
rs751694531 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482396 | TTAGGGTAGTCCAAG[C/T]CTCATGAGCACCGGT | 10580 |
rs751707335 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421033 | TAGGCTAGGTGTGGT[A/G]TCTCACACCTATAAT | 10580 |
rs751716502 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387643 | GTCTTTCAGATTCCA[C/T]TTCCCTATGTCATCT | 10580 |
rs751719879 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521826 | CATGCCCAGCTAATT[C/T]TTGTATGTTTTGCAG | 10580 |
rs751735431 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480563 | GTGTGACTTCAGGCC[A/G]GGCATTCAACCCCTC | 10580 |
rs751737355 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357099 | GCATTCCCACCTTTA[C/T]GATCCACTGGTAAGC | 10580 |
rs751741380 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95397269 | CTTGTACCAGTCTTT[C/T]GATCTCTCAGTGTTC | 10580 |
rs751765355 | snp | A/G | 3.30131e-05 | 0.00406269 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322834 | GCAAATTATAAGGGA[A/G]ACATTTTAGCAGATG | 10580 |
rs751770298 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515855 | CCAAATTTGGCCTAA[C/T]GCACCCTATGAGAGA | 10580 |
rs751775859 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318024 | TGAGATTCTGTCTCA[A/G]TAAATAAATAAATAA | 10580 |
rs751776125 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | SORBS1 | GRCh38.p7 | 10:95381765 | CACGATATTTTCTTG[C/T]GTCTACTTTCTTATC | 10580 |
rs751802331 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377022 | AACTAGTTGGAAAAT[G/T]AATGTGTGCAAAGCA | 10580 |
rs751803117 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511443 | TGGTCTCGAACTCCT[A/G]GCCTTAATCGATCCT | 10580 |
rs751815504 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95400290 | AAAGTACCCTGCCTG[C/T]GGCCACACAACCAGC | 10580 |
rs751822323 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357957 | CTGTCCTTTCTAAAG[A/G]GTGCTCTTATTTAGA | 10580 |
rs751842803 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458717 | TTTGGTGCTTCTGAG[C/T]TCATTCATTCAGTAA | 10580 |
rs751861222 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482745 | CCAGCACTGAGTATG[C/T]GCAGTATGTGACAGA | 10580 |
rs751865469 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | SORBS1 | GRCh38.p7 | 10:95399034 | GGAGTGGGATGCCCA[C/T]TTCATCCATGGAAAC | 10580 |
rs751865688 | snp | C/T | 0.000132837 | 0.00814868 | missense | SORBS1 | GRCh38.p7 | 10:95381695 | ATTACCATCTTTTCG[C/T]TGGTCAGAACGGAAG | 10580 |
rs751919432 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335624 | TCTTTGAGGTAGGTG[C/T]TATCATCTCCATTTT | 10580 |
rs751947757 | snp | C/T | 1.65452e-05 | 0.00287616 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394638 | GACTAGGAGTAGATG[C/T]AGGAAACTGGTAGGT | 10580 |
rs751959933 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443087 | TGAAAAACAAGTCCT[C/T]GGGATATGTAGAACC | 10580 |
rs751960443 | snp | A/G | 1.66549e-05 | 0.00288568 | splice-donor-variant | SORBS1 | GRCh38.p7 | 10:95432446 | CCCTAGCTTCCGCGC[A/G]CCTGGTTTGCTTTCG | 10580 |
rs751965669 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430132 | GACACAAAAGTATTC[C/T]GGGACAAGAGAGTGT | 10580 |
rs751970123 | snp | A/G | 3.31411e-05 | 0.00407056 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346495 | AAATCAGGATTCATG[A/G]ACAACAAGGACACAT | 10580 |
rs751971017 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334521 | GTCTGGAGGCCCACC[A/G]AGAAAGGAACACCAA | 10580 |
rs751977629 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459490 | ATTTAAAATACATTC[C/T]TTGTTCACTGCTGGT | 10580 |
rs751980301 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470172 | AGTCAAAGAATTACA[A/C]AAGTTAGACAGAACT | 10580 |
rs752014941 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418225 | CGAGACTATAGGCCT[A/G]TGCCACCACACCCGG | 10580 |
rs752022177 | snp | A/T | 1.67108e-05 | 0.00289052 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336940 | CACCGTCTCCATTCA[A/T]GTGAAGGGAGGCCTG | 10580 |
rs752022430 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557370 | GAAAAGGGAGTATTC[A/G]AAACACTATCTCATA | 10580 |
rs752025942 | snp | A/C | 0.000118071 | 0.00768254 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357018 | TTCTTGTGCTTACAC[A/C]CAGGGCCTAACGCAT | 10580 |
rs752039430 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539309 | CACTCTAAGATGTTC[A/G]GAAGCATGCTTGGCC | 10580 |
rs752046658 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324606 | ATGCTTCTTCTACAA[C/T]GACTCTGGACGTTAG | 10580 |
rs752056359 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489787 | TCTAGACAGCCAGCC[C/T]CCTGTGGCTGATCTG | 10580 |
rs752084853 | snp | C/G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386270 | TTTTTTTTTTTTAAG[C/G/T]CTGAGCTCTTTAAAA | 10580 |
rs752085652 | snp | C/G/T | 3.72053e-05 | 0.00431295 | splice-donor-variant, intron-variant | SORBS1 | GRCh38.p7 | 10:95414493 | AGTCCAGCAAGCTTA[C/G/T]GGTACTCGAAACAGC | 10580 |
rs752090685 | in-del | -/TT | 3.30759e-05 | 0.00406655 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397326 | AATTAAATGACTATC[-/TT]GACACATTTCAGACC | 10580 |
rs752092841 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407280 | TGACAATGGCCAATT[C/T]ACTAAACCTCTCGGC | 10580 |
rs752101405 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489052 | GTCTGGCTCTCACCT[A/G]CTGCTCTTATTTCAC | 10580 |
rs752126121 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378247 | CTGGCAAAGTTCTTT[A/C]GTACCACAGGCTATT | 10580 |
rs752129705 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446575 | ATCTCCTAGCCAGCA[C/T]GCTCCAGCTTCTCCT | 10580 |
rs752136966 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360510 | AAGCTTCAGCCAATC[C/T]CAGGCTGCCAACTGA | 10580 |
rs752152599 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407351 | ACTAAGGGGACCTAC[A/G]GTTCCCACACACTAC | 10580 |
rs752190808 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335498 | AGGAAGTTCTAAAAA[C/T]ATTCTCAGTTCTAGA | 10580 |
rs752193844 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555980 | ATTCTAAGCAGTACC[A/G]CAGTCACTGAGAAGA | 10580 |
rs752215801 | snp | A/G | 6.5912e-05 | 0.00574035 | missense | SORBS1 | GRCh38.p7 | 10:95341340 | TTAAACTTAGCAATA[A/G]CTTCTCCATATTCCA | 10580 |
rs752222877 | in-del | -/CC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548446 | ATAGTTCTTTTCTTT[-/CC]CCTTTTTTTTTTTTT | 10580 |
rs752230218 | snp | A/G | 1.671e-05 | 0.00289045 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341526 | GGTGCTTTGGGCACT[A/G]TCAGGCTTTTCCTTA | 10580 |
rs752247717 | snp | G/T | | | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311666 | GCAGATGGTAAATGA[G/T]TAAGGATGGAAAGGA | 10580 |
rs752254448 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342296 | GGACCTTGGACACAA[C/T]ACTTAATCTGAGACA | 10580 |
rs752255843 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476644 | ACTTCATAAGTGTTG[C/T]CAAGCAGCAGTCCCT | 10580 |
rs752296730 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325951 | ACCTCGGACTCTGAC[-/A]GGGGTAAAGGAAGAG | 10580 |
rs752305212 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | SORBS1 | GRCh38.p7 | 10:95410681 | TGACAATCGTTGTGG[A/G]GGGATAGGCGGATGA | 10580 |
rs752310066 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447087 | CGGAGGTTGCAGTGA[A/G]CTGAGCTCGCACCAC | 10580 |
rs752319029 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504967 | GGGAGAGTGAGGAGA[C/T]GAAAAGTAAAAGGGA | 10580 |
rs752325019 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383360 | GGCAGAGGGTGCAGT[A/G]AGCCGAGATCACACC | 10580 |
rs752329539 | snp | C/T | 0.000109443 | 0.00739659 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384402 | CCCTAGGGATCCCAG[C/T]GGACAGAAGAGTGAA | 10580 |
rs752337903 | snp | C/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312686 | ACCTGAATTTCTGGA[C/G]ATATACAAATGCGTG | 10580 |
rs752354939 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354395 | CAACTTCCTCAAATT[A/G]TTTTATAAAATGTAT | 10580 |
rs752367073 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517075 | AAAGCCCAAGTTACT[C/T]AGCCTTTCTCCGAGC | 10580 |
rs752369694 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363076 | TTGTTATTCACATTT[C/T]ATTTGCACCTCCTCC | 10580 |
rs752372129 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505607 | CAGCTGGAACAGTAT[C/T]AACTCCATTAAGACT | 10580 |
rs752376529 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428806 | TGGGGGACAAATGCT[A/G]TCCCTGGTGAGAAGG | 10580 |
rs752381998 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395255 | TTTGCCTGAATTACC[A/G]AGACACATAGAAAGA | 10580 |
rs752385347 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408100 | GAAAAACCCTAGGGT[A/G]ATCCCTAGACTGCTT | 10580 |
rs752398155 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533929 | AAGCTGGATTTATTA[C/G]AAGAAGATAAAAGAA | 10580 |
rs752412132 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353373 | CCTGATGGACACTCA[-/T]CATTAGTGAGTTATT | 10580 |
rs752417521 | snp | A/G | 3.32674e-05 | 0.0040783 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410797 | AACGAACAAACAAAC[A/G]ATGTAACTAACTGTA | 10580 |
rs752424305 | in-del | -/AAAA | 0.000130368 | 0.00807261 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367731 | AAGAAAAAAAAGAAG[-/AAAA]AAATAATGTAGATGA | 10580 |
rs752429639 | snp | C/G | 1.81632e-05 | 0.00301351 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384342 | AGGTAAGAGAACCAA[C/G]TTGTATGTTCCCCAT | 10580 |
rs752440444 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434796 | GAGGAACTGGGCAGG[C/G]ACAATAGGAGGAAGT | 10580 |
rs752450361 | snp | C/T | 1.65987e-05 | 0.00288082 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336928 | GCGTGTGGACACCAC[C/T]GTCTCCATTCATGTG | 10580 |
rs752479112 | snp | G/T | 1.64803e-05 | 0.00287052 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414762 | AGAGGCCCCAGAGGT[G/T]TTGGAGGTCTGGCAG | 10580 |
rs752486573 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330059 | GGAGGCTCTTAACCT[A/G]GTGATCTGTCACAGG | 10580 |
rs752491723 | snp | A/T | 3.38748e-05 | 0.00411537 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371467 | AAAGAAGGTTTTAGT[A/T]TAGAGGAAAGGGAGA | 10580 |
rs752531525 | snp | C/T | 1.68004e-05 | 0.00289826 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434739 | ACACAAAAGGGTAAA[C/T]GGTGCATCCAGAAAG | 10580 |
rs752534000 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425682 | TTCCCCTATCCCAAA[A/G]AGGCAGTTCTCAGGA | 10580 |
rs752538037 | snp | A/C | 1.65833e-05 | 0.00287948 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315150 | AAACACACACATACA[A/C]AACATGAGAAGACCC | 10580 |
rs752541452 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328899 | CTCTATTATATTTCA[C/T]TTAATTCTCATAGCA | 10580 |
rs752556434 | snp | C/T | 4.98434e-05 | 0.00499192 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95315062 | TTTTCAGTCTTCTTA[C/T]AGATACAAAGGTTTT | 10580 |
rs752576430 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331468 | ACCGTGACTCCTGAC[A/G]TAACTTCTGGTCCCA | 10580 |
rs752584290 | snp | A/C/T | 0.000195364 | 0.00988162 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339117 | TATGAAAACCAGTGA[A/C/T]GAGAAGCTTAGATAC | 10580 |
rs752605323 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460176 | GGGGAAAAAGAAACA[C/G]CAATTCGTTACAAGA | 10580 |
rs752633231 | snp | A/C | 0.000277816 | 0.0117827 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355467 | GCTTTGTTTTTAAAG[A/C]AGTGCAGCCACTACG | 10580 |
rs752657952 | snp | A/G | 3.38478e-05 | 0.00411373 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414843 | ACCTCCGGCTGGGCT[A/G]CACTGGAGGAAGTGG | 10580 |
rs752658596 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549920 | TACCAATGCATTTGA[C/G]TCCCCCAACTCCATA | 10580 |
rs752667824 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403664 | CCTCCCTGTTTCAAG[C/T]GATTCTCCTGCCTCA | 10580 |
rs752679768 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479403 | CATCTTCTTACTTTA[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs752689599 | snp | A/G/T | 0.000148363 | 0.00861168 | missense | SORBS1 | GRCh38.p7 | 10:95384018 | AGTGAGGAAGAGCGG[A/G/T]CTGGGAGGGGTAGTG | 10580 |
rs752696380 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552934 | ATAAAAAGGAACAAG[A/C]GCAGGCACGGTGGCT | 10580 |
rs752725132 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484823 | TACAAAAAAATACAA[A/C]AATTAGCTGGGCATG | 10580 |
rs752758951 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503120 | TAACCAAGAGAAACT[G/T]CTCCTTAGAAGGTAG | 10580 |
rs752763769 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491300 | GGATCTTTAATTCAC[C/T]AGCTGAAATGGTCCC | 10580 |
rs752778842 | snp | C/G | 1.65138e-05 | 0.00287343 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95339205 | ATCCACAGGGTTTTT[C/G]ACCAGTGGTCGCTTG | 10580 |
rs752780871 | snp | A/T | 2.34502e-05 | 0.00342412 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336482 | GCCCACCCTGCCAAG[A/T]GAGACGCCAAGTGCA | 10580 |
rs752792096 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451454 | CAGTTTCTAAAATAC[A/G]CAGTTAACCAAGACA | 10580 |
rs752793344 | snp | A/T | 0.000842916 | 0.0205121 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357060 | AACGTTCGGCTATGG[A/T]CTGAAGATGAAGAAA | 10580 |
rs752819071 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354514 | AGTATTGGAGAAATA[C/T]GCAGGTGGATTTCTT | 10580 |
rs752835479 | in-del | -/AAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428414 | GAGACTCCATCTCAA[-/AAA]AAAAAAAAAAAAAAA | 10580 |
rs752841861 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440664 | TTTTACTACCAAAGG[C/T]AAAGCAAAAGAGGGA | 10580 |
rs752842099 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531165 | CACCAAACTGCGAGC[C/T]AGAGCCCCATTTCAC | 10580 |
rs752857118 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492552 | CCCCTGAGCTAAACC[C/G]TCTACGGTAAGTGTA | 10580 |
rs752894931 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534246 | GTCGCTGGGATTACC[A/G]GTGCCTGCCACCATG | 10580 |
rs752895089 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95532422 | TGGCTCAGGAAATGG[G/T]ATCCCCTTTCAGTCA | 10580 |
rs752896559 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315218 | TGCTCCAAAACCCCT[C/T]GTAACAGTCCTGCAG | 10580 |
rs752897313 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520148 | AAAATGGAGAAACCC[C/T]ATCTCTACATACAAA | 10580 |
rs752901684 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480258 | TAAACTAGGACAAAC[C/G]GGAAAGGGAAGGGGA | 10580 |
rs752910477 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480744 | CATGCCAGGTCCTCC[A/G]CTGGGTACGAGGCAC | 10580 |
rs752935484 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390544 | TTTCTTCATCTCTTT[C/T]TGGGGGCTGGGAAGA | 10580 |
rs752939075 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386224 | TTCACTGGGTGGAGA[A/G]GAGTGGCATTTAAAT | 10580 |
rs752955856 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479668 | GAGGTCAGATGATCC[A/G]TGGCGATCTGGAACC | 10580 |
rs752960428 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411169 | ATTGGGAAAAATCAG[A/G]GAAGTTTAGTACACT | 10580 |
rs752988226 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428327 | TGAGGCAAGAGAATT[G/T]CTTGAACTCAGGAGG | 10580 |
rs753007140 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397588 | GAATCTCTCCATATA[C/T]AGACTGTGCCAAACT | 10580 |
rs753099547 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339128 | GTGACGAGAAGCTTA[A/G]ATACCTGTGGGCTTG | 10580 |
rs753114515 | snp | A/G | 1.6607e-05 | 0.00288153 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346504 | TTCATGGACAACAAG[A/G]ACACATTTTCACAAA | 10580 |
rs753120118 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357558 | CCCATTGCTGGAGGT[C/T]CACCACGGCCGACGC | 10580 |
rs753147710 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542915 | AAGCATGACCAGGCC[C/T]GATCCCTGCTAAGCA | 10580 |
rs753179667 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537361 | AAGGAAGACACACAG[A/T]GACATGCTGGAGAAG | 10580 |
rs753203352 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334216 | GCTGCCAGAGAACAG[C/T]TGTCATACAAGTCCT | 10580 |
rs753211607 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | SORBS1 | GRCh38.p7 | 10:95318374 | CGATATCTCCATCGC[A/G]GAGTTCCAACTCATC | 10580 |
rs753223966 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526330 | CTGGCGCACCTGCAG[A/T]TCACCTGGGCAGCCT | 10580 |
rs753232966 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538360 | GAGGTCACCATCTGA[A/G]ATATGTCCACAGAGC | 10580 |
rs753247913 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548114 | GTGCAGGCAAGCCAG[A/G]AGAAAGGAGATACTG | 10580 |
rs753265281 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458429 | TAACATTTATATAGG[C/T]CCAAGTGTCTCTAAA | 10580 |
rs753294059 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487869 | CAACTATCTACCACA[A/G]CCATCACAGTATATT | 10580 |
rs753294788 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336859 | GGGAGATGACACTAT[C/T]AGAGCTCCCCAGCGG | 10580 |
rs753314843 | in-del | -/CTC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95495781 | ACGACATACTCTCTT[-/CTC]CTTCTCCCTCCACAA | 10580 |
rs753327424 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347721 | GATTACAGGTGTGAA[C/T]CACTACGCCCGGCTG | 10580 |
rs753328386 | in-del | -/GTCTTAGAGAACAT | 1.65274e-05 | 0.00287462 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321918 | TTTCTAAGACCAACA[-/GTCTTAGAGAACAT]GTCCTCTGAGAACAT | 10580 |
rs753333599 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555033 | ACTACAGGCATGCGC[C/T]ACCACGCCCGGCTAA | 10580 |
rs753343157 | snp | A/C | 0.000227946 | 0.0106734 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415876 | CATGACATGGGTTAG[A/C]GCTCACATTCTTATG | 10580 |
rs753358297 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458001 | TAAGTCTATAAAAGA[A/C]TAAAATATCCCTACC | 10580 |
rs753359976 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375225 | CTAGAGTTTTAAAGT[C/T]AGTTTCGTTATCTCT | 10580 |
rs753381815 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334014 | GGTTCTCAGGTAAAA[C/T]TCCCTCCCATTATTG | 10580 |
rs753396277 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416820 | AGGATTTTTGAATAC[A/G]CATGTGCTCTTTTCT | 10580 |
rs753410951 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407604 | AGCCTGGGTGACATA[A/G]AAAGACCCTGCCTCA | 10580 |
rs753436518 | snp | A/G | 3.74953e-05 | 0.00432969 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414472 | CAGAAAAGCCGTGAG[A/G]AGGGGAGTCCAGCAA | 10580 |
rs753441127 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347773 | GAGACAGCGTCTTGC[C/T]CTGTTGCCCAGGATG | 10580 |
rs753445420 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352465 | ACCCCTAAAGGAGGG[C/T]GGGCCCGATTTTTCT | 10580 |
rs753447041 | snp | G/T | 4.18524e-05 | 0.00457432 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384411 | TCCCAGCGGACAGAA[G/T]AGTGAAGCGCCAGAA | 10580 |
rs753472168 | snp | A/G | 1.72142e-05 | 0.00293374 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414855 | GCTGCACTGGAGGAA[A/G]TGGCATCCTGTGGAA | 10580 |
rs753485793 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446335 | ATGACCCTATAATTC[A/T]AAGATAAGTTTTGAT | 10580 |
rs753493533 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555857 | CTTTTCCAAAAGGGT[C/G]TGGGTCCTGCTACAG | 10580 |
rs753507033 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516511 | TCTCACAGCAGTGCT[G/T]AAGTAGATAAGCTGC | 10580 |
rs753507366 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504697 | GAGTAATACACCTAC[A/G]TGCTTAGCACAATGT | 10580 |
rs753515818 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529427 | TTATTGTCCAGTTCC[G/T]GTAGACATACAGCTG | 10580 |
rs753517921 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393653 | TGGACTCAGTCAGCT[C/G]AAGTGACCTTGCTGA | 10580 |
rs753523182 | in-del | -/TCATGC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383810 | TATCCTTACTAGGAA[-/TCATGC]TATTTTTATCCCCAT | 10580 |
rs753528490 | snp | C/T | 1.70345e-05 | 0.00291838 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434757 | TGCATCCAGAAAGAA[C/T]ATTTGGGAAACACTC | 10580 |
rs753533079 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487764 | CAGCTGCATTTTATG[A/C]CAGAAGCCCACAAAT | 10580 |
rs753535724 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433313 | TCTCCTACAGTTTCA[C/G]TAGGGCCTAATAACA | 10580 |
rs753535744 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476233 | TATTTTAAATGTTGG[A/G]CTCTTGCTTTAAAAG | 10580 |
rs753551090 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543745 | GGATCTCTACCGAAC[C/T]CAAAACATAATAAAT | 10580 |
rs753556824 | snp | A/T | 1.64944e-05 | 0.00287175 | missense | SORBS1 | GRCh38.p7 | 10:95339227 | GGTCGCTTGATCACA[A/T]CCACGTAGGTGATGG | 10580 |
rs753566301 | snp | C/T | 1.6651e-05 | 0.00288535 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315167 | ACATGAGAAGACCCA[C/T]TCGCTTGAGTTGAGA | 10580 |
rs753571892 | snp | A/G | 1.65274e-05 | 0.00287462 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394617 | TTTAATTACCTTCAG[A/G]TTTAGGACTAGGAGT | 10580 |
rs753573909 | snp | A/C | 1.66363e-05 | 0.00288407 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371949 | CAAGGCTAGAGAGCA[A/C]ACACAGTCCAACGGA | 10580 |
rs753587825 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463919 | TGGTCACAAATGTCC[C/T]GTTCTCCTGCCATTG | 10580 |
rs753605038 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382463 | TGGGTTGAGACCTTA[C/G]ATTCAAGTCAGTAAT | 10580 |
rs753624876 | in-del | -/A | 0.000165906 | 0.00910635 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367718 | ACATGTCCAAAAAAG[-/A]AAAAAAAAGAAGAAA | 10580 |
rs753636436 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394047 | CAGCTCTTTCATTAA[A/C]TGTTTTCCAGCTTAG | 10580 |
rs753645613 | snp | C/G | 0.000121264 | 0.0077857 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355588 | CAAGCAAAGTGGAGG[C/G]ACGGGCAGGTGAGAC | 10580 |
rs753658047 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328707 | CCAAAGTAAAATGAT[G/T]TTCCCATCATTCTCT | 10580 |
rs753670540 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95412138 | ATTATGATAAATGAC[A/G]TATCATTAAAAACTG | 10580 |
rs753675211 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423491 | GCACAGGCCAGATTC[C/T]GCTCACAGCCACAGT | 10580 |
rs753682127 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95341185 | TCTTAAGGGTACAGA[C/T]AGCACCCCCAGACTG | 10580 |
rs753685730 | snp | A/T | | | downstream-variant-500B | SORBS1 | GRCh38.p7 | 10:95311630 | AGGTAAGAAGTGGTG[A/T]CTTCAAGGAGGCGGC | 10580 |
rs753694806 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522075 | AAAAAGGATGAAGAC[A/T]CATCACTAACTTCAA | 10580 |
rs753730437 | in-del | -/CT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403215 | TTCATTCCCAGATGA[-/CT]CTCCCTGAACATCAA | 10580 |
rs753740730 | snp | A/G | 0.000131848 | 0.00811828 | missense | SORBS1 | GRCh38.p7 | 10:95384027 | GAGCGGGCTGGGAGG[A/G]GTAGTGTGGCCGACC | 10580 |
rs753744116 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383306 | CTGCAGTCCTAGCTA[A/C]TCGGGAGCCTGAGGC | 10580 |
rs753745161 | in-del | -/TTTTTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499064 | TGTGAGTCTATAATG[-/TTTTTTT]TTTTTTTTTTTTTTT | 10580 |
rs753746603 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366056 | ACCACAATATCTGTC[-/A]AAAAAAAAACCTTAT | 10580 |
rs753771568 | snp | A/G | 1.70717e-05 | 0.00292157 | missense | SORBS1 | GRCh38.p7 | 10:95339306 | TCTCATCTACCTGCC[A/G]GAGCAGTGTGATCCT | 10580 |
rs753794533 | snp | G/T | 1.65482e-05 | 0.00287643 | missense | SORBS1 | GRCh38.p7 | 10:95399187 | TTCTTTCTGAGACAG[G/T]ATCTGGAAATGAAAA | 10580 |
rs753798235 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370583 | CCTTTTCCTTTTAAG[A/G]GTCTCTTTTGTTTTG | 10580 |
rs753811173 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95493899 | ATTGCGATGTCCAAT[A/G]TGAAAAGAGTGTATT | 10580 |
rs753812181 | in-del | -/A | 0.000165906 | 0.00910635 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367719 | ACATGTCCAAAAAAG[-/A]AAAAAAAGAAGAAAA | 10580 |
rs753819530 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413085 | ACAAGCCATTTGGAA[C/T]AGTTTTGCAGGCATA | 10580 |
rs753832569 | snp | A/G | 3.74995e-05 | 0.00432994 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357830 | TAATTTTGAAAGAAA[A/G]AGAGAAAAGGGAAAA | 10580 |
rs753841454 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452554 | ATTACAATACAAATT[A/T]CTGTAATGAGTTTTC | 10580 |
rs753844086 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523086 | AAACCATTACCTCAT[A/G]CTTTTGCACTTGAAC | 10580 |
rs753853304 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369495 | TCAATTACCTAAAGC[C/T]AACTCCCTCACCTTG | 10580 |
rs753873277 | in-del | -/TG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436929 | TCTGTGCAGCCACAC[-/TG]AGGTCAGGATGAAAG | 10580 |
rs753889119 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390322 | AGTCAGGAGAAGCCA[C/T]GGACCATGAAGTAAC | 10580 |
rs753889624 | in-del | -/TGGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373746 | TCTTTTGTGGCAGAG[-/TGGT]TGGTTGCAGTAGGAA | 10580 |
rs753920261 | snp | A/C | 1.65592e-05 | 0.00287738 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384149 | ACAAAAGACTTAAAA[A/C]TCATGAAAACTGAGA | 10580 |
rs753920370 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95373706 | CAGCTTCCATGGTTT[A/G]TGCCACTTTTATTTA | 10580 |
rs753929503 | snp | A/G | 1.65255e-05 | 0.00287445 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336629 | ACCCAGGGGCTTGCC[A/G]GGCCGGCTCTCCTCA | 10580 |
rs753942307 | snp | A/T | 1.65364e-05 | 0.0028754 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394972 | ATTTAAAGCTCGGAC[A/T]ACAGATATGCTGTCT | 10580 |
rs753952488 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320827 | CTTCCTAACACAGCA[C/T]CTGCCACCACCCCTA | 10580 |
rs753957490 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421683 | GGCTAAATGAATTCC[C/T]TCTTTCAGAACACTT | 10580 |
rs753961993 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351020 | GCATGCTTGAACATA[A/C]AGAGCACAGGACATA | 10580 |
rs753980889 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464300 | CTCCAGCCTGGGAGA[C/G]AGAGCGAGACTCTGT | 10580 |
rs753984327 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529726 | TAAGAAAAATGAAGC[C/T]CAAAGTAGTGCAGTG | 10580 |
rs753989809 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501953 | TCCCAGCAGGCTGTT[C/T]GTTCTGGGGCCTTTA | 10580 |
rs753990996 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95420522 | GAAAGGGTTTAGGGA[C/T]GGGAAAACCATGGCA | 10580 |
rs754003073 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410145 | TTCAAGGTACAAAAA[C/T]GTGTTTTACATTCCA | 10580 |
rs754003251 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500087 | GACCCTTAGGGTGTG[C/T]GTTCCCCCACCTTTC | 10580 |
rs754008772 | snp | A/C | 1.65622e-05 | 0.00287764 | missense | SORBS1 | GRCh38.p7 | 10:95357757 | TGAGATCCCCAGGAG[A/C]CCCGTCTGATTCCCT | 10580 |
rs754028732 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380983 | CTTTTCCCAATGAAG[G/T]GTTAATAAAAGGATG | 10580 |
rs754032353 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507984 | GTAGTGGCCCAGACT[-/TT]TTTTTTTTTTTTTTT | 10580 |
rs754035542 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518762 | CTGGCTTGGAATGAA[A/T]CAAAGATAAGTAATA | 10580 |
rs754044092 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491220 | TTGCCAGGCAATTTA[A/G]GCATAAACCCCTATC | 10580 |
rs754065843 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95414212 | AGCATGGCCAGTCAA[A/C]ATAAAGGCCACAGAT | 10580 |
rs754066933 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95338865 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 10580 |
rs754068814 | snp | C/T | 4.94222e-05 | 0.00497078 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351301 | GGTGCGTCGGAATGA[C/T]GCCTGTGTGGCGTCG | 10580 |
rs754083514 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379757 | TGTGTGTTTTGGGGC[A/G]ATGGGGGTGTATGCT | 10580 |
rs754084074 | snp | C/T | 1.69723e-05 | 0.00291305 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414627 | AAGGAGCCAGAGGCG[C/T]GGGCTGGCTGGCTGT | 10580 |
rs754118142 | snp | A/G | 0.000115326 | 0.00759274 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351273 | CCAAAGCGCTCATTA[A/G]TGATAAACTGATGGT | 10580 |
rs754122056 | snp | C/T | 1.67211e-05 | 0.00289142 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432606 | TCCAAAATTGAAGAC[C/T]GAATCCAAGACTCCT | 10580 |
rs754133975 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438100 | TTTATCCTGAAGACC[C/G]AGACCTCCAGAACTA | 10580 |
rs754139299 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409132 | ACTTGGCAGAAGCAG[C/T]TGACATTACACTTGG | 10580 |
rs754151255 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479334 | CTCTAAGACTGAAGA[C/T]ACCGGGCTTGTTCCA | 10580 |
rs754182419 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559330 | GAAGAATTTGCTCAT[C/T]CTTTCCCATAACTCC | 10580 |
rs754183682 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328176 | ATAGTGATAGATTTG[C/T]ACCTACTGGAACATC | 10580 |
rs754186260 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337653 | ACATTGGAAGCTCCC[-/C]ATCCCAGCCAACCCA | 10580 |
rs754202402 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480505 | CATGGCATTTGGAGT[C/T]AGAGGAGGTGAACTT | 10580 |
rs754209303 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334644 | CCCTAACCTTACTCG[A/G]AGATCCGGCACCGTG | 10580 |
rs754210210 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552275 | GGCGTGGTGGCATGC[A/G]CCTGTAATCCCAGAT | 10580 |
rs754211726 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355697 | GTCTGAGTATGGCAC[C/G]GAGTTTCCATTATTA | 10580 |
rs754236334 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450831 | ATATAATAGGCAAAA[C/T]GCATGTATATAGTAA | 10580 |
rs754252615 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548583 | ACCTCAGCCTTCCAA[A/G]TAGCTGGGACTACAG | 10580 |
rs754259253 | snp | G/T | 3.56201e-05 | 0.00422005 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337129 | AGATAGAAGCCTCTG[G/T]CAGAGGAGGCAAGGG | 10580 |
rs754272542 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547392 | TGAAGAAATAAACAC[C/T]TGCAGGGTGGGGCCC | 10580 |
rs754276377 | snp | A/G | 1.64939e-05 | 0.0028717 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395058 | ACGTAGGGAAATAAG[A/G]GTTTTCTTCAGGAGT | 10580 |
rs754286129 | snp | C/T | 0.000121029 | 0.00777816 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356287 | TACATGTTGGGGAAG[C/T]ATAGACCCCACTGGA | 10580 |
rs754301281 | snp | G/T | 1.76717e-05 | 0.00297247 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422104 | GAAAAAATCTCTCAC[G/T]CACAGGGAATAACTC | 10580 |
rs754303309 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537224 | TTCATCCAACAAATA[C/T]GTACTGCCTGCTTGT | 10580 |
rs754317457 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536340 | AAGGAACAATGCCGG[C/G]GTTTAGGAAAGTGAA | 10580 |
rs754321175 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346372 | TTCAAAAAGGCAGCT[A/T]AAAAGACAAATAAAT | 10580 |
rs754361161 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476792 | GTGATTTTTCTCCTT[-/A]AAATCTTTTTCCATA | 10580 |
rs754372459 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356630 | GGAGCCCAGGAAGAG[G/T]CCAGATCGGTTGATC | 10580 |
rs754373813 | snp | A/G | 3.56468e-05 | 0.00422163 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377332 | AAAGCAGCTCTTCTT[A/G]TACTTTACTTACAAC | 10580 |
rs754377830 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386016 | GATTAGAAAAAATGC[C/T]GCAATGAAAATGCCC | 10580 |
rs754383839 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540759 | CTTAAGTTTCCCAAA[A/G]ACTAGCTTTGTGGAG | 10580 |
rs754386791 | snp | A/G | 1.65187e-05 | 0.00287386 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95422003 | ATGCACACTTCTGTA[A/G]CCCTTGGCAGCGAGT | 10580 |
rs754388020 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508668 | GAGTGGCTCCTAGAG[A/G]GTGAGTTCCTCATTG | 10580 |
rs754400503 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468343 | GCCATTTTGTTAAGG[C/T]ACCCACGCAAGGAGC | 10580 |
rs754403163 | in-del | -/C | 3.31444e-05 | 0.00407076 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410792 | CCTGAAACGAACAAA[-/C]AAACAATGTAACTAA | 10580 |
rs754408025 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95311807 | AAGTTTATTAAATAA[C/T]ATGTACAGCAAATGT | 10580 |
rs754427651 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455887 | GCTGCAGTGAGCCAT[A/G]ATTCTACCATTGCAC | 10580 |
rs754428556 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398437 | AGGGCCTGCAGGACT[A/G]GCAGGCCTGTGCTGC | 10580 |
rs754430678 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385367 | CATGGAATGAAGACC[C/T]AATTCCTTCCCTAAA | 10580 |
rs754440809 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497497 | CTTGAAAAATTCAGA[C/T]ATCCATAGCCGTGTC | 10580 |
rs754448465 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362293 | ATGTGGATCAGTAGA[C/G]GCAAACCCACTCTTG | 10580 |
rs754462021 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406254 | TGAGTCCTCACTGTC[C/T]TCTGGACTTAGATGG | 10580 |
rs754473062 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327266 | CATGCATACACACAT[-/AC]ACACACACACACACA | 10580 |
rs754487062 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95392447 | ACCCTATTTTTAAAA[G/T]ATCTCCAGGGAGGAT | 10580 |
rs754507150 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526251 | AACTCCAAGGCTGCC[A/G]CACCTTATCTTAATC | 10580 |
rs754513907 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404951 | TAGCTACACATTCCC[C/G]TTCCTGGGTTCCCTC | 10580 |
rs754528789 | in-del | -/C | 2.19358e-05 | 0.00331171 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336500 | GACGCCAAGTGCACA[-/C]GCGGCATGCTGCAGT | 10580 |
rs754541206 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375300 | TGGGTGCAAGGCTAA[G/T]AAAATCCTCCTTTAA | 10580 |
rs754549087 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548162 | AGGACCAGTGACCAG[C/T]TGTGACACTCAGAGG | 10580 |
rs754555730 | snp | A/G | 1.7621e-05 | 0.0029682 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339349 | GACACAGCAAAGAGA[A/G]GGTCCTTGTCCTAGC | 10580 |
rs754562894 | snp | A/T | 1.81516e-05 | 0.00301255 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367644 | CAAAATAAAATGGCA[A/T]CTTACTATCCAGGAG | 10580 |
rs754567506 | snp | C/T | 0.000115717 | 0.00760559 | missense | SORBS1 | GRCh38.p7 | 10:95421983 | TTGTCAGAAGGAAGG[C/T]TGGGATGCACACTTC | 10580 |
rs754569779 | snp | A/G | 1.70235e-05 | 0.00291744 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399230 | TGAAGCTCTTTTGGT[A/G]GCTGCAAAACAAAAC | 10580 |
rs754571356 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353143 | ATGTAACTTCTAATA[C/T]ATCAATTGCTAAACC | 10580 |
rs754582905 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503717 | TGTGGCCTTGGGCAA[C/G]TTTCTGAACCTCTCT | 10580 |
rs754593868 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492801 | CTCTGGGTCTTAAAA[G/T]CCCCTGCCTGATGCC | 10580 |
rs754607967 | snp | A/T | 1.65042e-05 | 0.0028726 | missense | SORBS1 | GRCh38.p7 | 10:95341304 | CTGAAGGACATTTCT[A/T]CTTGTGTATCACCAT | 10580 |
rs754640988 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543752 | TACCGAACCCAAAAC[A/G]TAATAAATGAAAAAA | 10580 |
rs754642966 | in-del | -/CACC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432332 | ACACACACACACACA[-/CACC]CCCCCCCCCCAAGAG | 10580 |
rs754655100 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393789 | ATGAATGAAGTTCAG[A/G]GCACTCAACATCTCA | 10580 |
rs754656995 | snp | A/C | 1.6582e-05 | 0.00287936 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384212 | TCCCTTCCGCCCCCA[A/C]AACCAGGTTATTTGA | 10580 |
rs754673892 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434141 | TGGGGAAGGCAAAGG[A/G]GATGCTCTGGGATGG | 10580 |
rs754676136 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336746 | GGGTCCACCAGGGCC[C/T]CTTTCGCCTGCCCCC | 10580 |
rs754679668 | in-del | -/ACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524697 | TGGCCCGCAAAGCTG[-/ACA]ATATTTACCATCTAG | 10580 |
rs754693254 | in-del | -/TGGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498138 | ACAGGCAGAAAGGTA[-/TGGT]TGGTACAAAGAGTAC | 10580 |
rs754698277 | snp | A/G | 1.64822e-05 | 0.00287068 | stop-gained, intron-variant | SORBS1 | GRCh38.p7 | 10:95336670 | GATCTGAGAGTCTCT[A/G]TTCAGTACTCAGGCA | 10580 |
rs754701682 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434655 | CTGAGGCGTTTTTCA[C/G]TGTCTTCACAGGAAT | 10580 |
rs754701741 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451726 | ATTTTTCTTCTGAAG[C/G]AGTCGCTATACAATG | 10580 |
rs754703279 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358214 | AGCTCTCTGTCAGAC[A/G]TGCCTCTGTCACGTA | 10580 |
rs754723628 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95381745 | GTAAATGCTCTTGGG[C/T]TCTGCACGATATTTT | 10580 |
rs754724231 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95351317 | GCCTGTGTGGCGTCG[A/G]GCTGCAATATCAGCC | 10580 |
rs754728954 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423493 | ACAGGCCAGATTCCG[C/T]TCACAGCCACAGTTT | 10580 |
rs754760467 | snp | C/G | 1.67506e-05 | 0.00289396 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371318 | GCATGAGAAAAACTA[C/G]GAAATACCTGTGGCA | 10580 |
rs754784234 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369750 | CACAGCCACAGTCAC[A/C]ATTCTCACTCCAGGG | 10580 |
rs754786400 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533043 | TCGTAAGTCACTCCC[C/T]CCCTATGGTACCGTA | 10580 |
rs754823494 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522186 | TGCAGAAGTTCTGAC[A/G]GGGTCCCAAGGCCCA | 10580 |
rs754825623 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434588 | GCCATGATCCGCTCA[C/T]AGTTAGAGAAAATCG | 10580 |
rs754839361 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533748 | TACCTGGACCTCTGT[C/T]CTTGTGGACCTCAGC | 10580 |
rs754882097 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95483667 | TAGCTGGGATTATGG[G/T]TGCCCGCCACCATGC | 10580 |
rs754897973 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452594 | AGATAAAACCACTAA[A/T]ACATTCAACATAATA | 10580 |
rs754901846 | snp | A/G/T | 3.75631e-05 | 0.00433364 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337226 | AGCGTGCATCTCGGG[A/G/T]GACAGGGCTCGGCGG | 10580 |
rs754921468 | snp | A/G | 1.65938e-05 | 0.00288039 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351401 | AATTGCATAAAATGG[A/G]CAGTGAATCATCTGT | 10580 |
rs754935076 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348110 | CCAAACGTACGGGGG[A/C]CAAGTGAATGATCAC | 10580 |
rs754938707 | snp | A/C | 4.94458e-05 | 0.00497197 | missense | SORBS1 | GRCh38.p7 | 10:95397271 | TGTACCAGTCTTTTG[A/C]TCTCTCAGTGTTCTG | 10580 |
rs754949816 | snp | G/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441859 | CCTTAATTTAGTAGG[G/T]TCTCAAAGAAAGCTG | 10580 |
rs754972982 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95379762 | GTTTTGGGGCGATGG[A/G]GGTGTATGCTCAAAT | 10580 |
rs754982192 | in-del | -/AAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95428413 | TGAGACTCCATCTCA[-/AAAA]AAAAAAAAAAAAAAA | 10580 |
rs754989822 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470527 | TCAGGTCACCACCCC[C/G]ACTGCCTTGTAGTCC | 10580 |
rs754994406 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370609 | TTTTGTCAGGGAGCC[C/T]TCCAGGCAGTTCTAT | 10580 |
rs754999484 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409173 | AAACCAAGTTGCCTT[C/G]GGAATAAATCCCATT | 10580 |
rs755000223 | snp | C/T | 3.36536e-05 | 0.00410191 | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315044 | TAAAAATAATCTCCA[C/T]GGTTTTCAGTCTTCT | 10580 |
rs755003671 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500818 | CTCTATGATGTTAAA[C/T]GAGTTCTCAATCTCT | 10580 |
rs755013204 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365970 | AAAATACCCAAATCC[C/G]TGCTGACTTTCAAAT | 10580 |
rs755015392 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529028 | GGAGGACCCTACAAA[A/G]ACGGTCAGTTTGGAA | 10580 |
rs755017401 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540781 | TTTGTGGAGGTTAGG[G/T]AGGAGGTCACTAGCC | 10580 |
rs755026669 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | SORBS1 | GRCh38.p7 | 10:95395123 | AGAGGAAGATACAAA[C/T]GGAGAGAATAAACGA | 10580 |
rs755042940 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448593 | TACTTTGCACCCAGG[A/T]AAGTGCTTGGCCCAG | 10580 |
rs755043996 | snp | A/G | 4.39116e-05 | 0.0046855 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422152 | TCCGGGGTCCTTGGT[A/G]GAAGGCCAGAAAGGT | 10580 |
rs755058775 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490213 | ATTAAGTTTCTTTCA[A/G]AAAAAGGAAGAACAT | 10580 |
rs755058968 | snp | A/C | 3.31252e-05 | 0.00406958 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322705 | GGATCAGTAAAAATT[A/C]TCTTTAGAAAAGCTG | 10580 |
rs755060142 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95350769 | TGGCATAAATTATTG[C/T]TAAGCTAACTTTCGT | 10580 |
rs755064218 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421816 | CCTTAGCTAGGTCCT[C/T]GCAGAGCTTATCCAG | 10580 |
rs755072337 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529808 | AGCTAGAAATAAGAA[C/T]AGATGCCTCACATTA | 10580 |
rs755097268 | snp | C/T | 5.36438e-05 | 0.00517871 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339083 | CAGCACTGTTGACTA[C/T]AAAAATTCACATGCT | 10580 |
rs755102594 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95378861 | GGCCATTTCTGACAA[A/G]GCAAGGACTGACCAA | 10580 |
rs755120073 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95314250 | GCAGCTGCACTGTCC[C/T]GAAGGTAACCATTTC | 10580 |
rs755131269 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501997 | GTCATCTCACTGAAC[C/G]TGAATGTTGGACAGG | 10580 |
rs755132061 | in-del | -/CTGGGATTACAGGCCTTAATGCAATTC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340828 | TGGTTTCCCAAAGTG[-/CTGGGATTACAGGCCTTAATGCAATTC]TTTTTTTTTTTTTTG | 10580 |
rs755139155 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519784 | CTAAGTCATCCCAAC[A/C]TGAAGCTGCCTCATA | 10580 |
rs755157772 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518768 | TGGAATGAATCAAAG[A/G]TAAGTAATAAGGGAA | 10580 |
rs755162144 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410155 | AAAAACGTGTTTTAC[A/G]TTCCAGAAAATTGTC | 10580 |
rs755183993 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387410 | ATGGAAGGATATTTT[A/T]CCTCAGCTTATGAAT | 10580 |
rs755187000 | snp | C/T | 0.000272628 | 0.0116722 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355770 | GAGGGCTCTGAGCTG[C/T]GGCTAAGCCTGGCCA | 10580 |
rs755198926 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476977 | ACCAAGATAGAGCTA[C/T]TCCTTTGACTCAGTC | 10580 |
rs755202224 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506813 | GTTTGAGGGCGAAGG[-/T]TAAGAGAAATCCTAG | 10580 |
rs755208773 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95326785 | TCTTCTGGACCTATC[C/G]TGTCCAAGATTGTAG | 10580 |
rs755211053 | snp | C/G | 1.6566e-05 | 0.00287797 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341560 | AGAAAAGAGGCTGCG[C/G]TACCTCGATGTAGGT | 10580 |
rs755236654 | snp | A/C | 0.000449539 | 0.0149856 | intron-variant | SORBS1 | GRCh38.p7 | 10:95386945 | AGCGAGATCCCATCT[A/C]TACAAAAAAATTTTT | 10580 |
rs755242116 | snp | A/G | 0.000260396 | 0.0114075 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422223 | GCTCCAGACCTACAC[A/G]TGGTGCAGAAAGGAT | 10580 |
rs755281550 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520055 | CTGGGCACGGTGGCT[C/T]ACACCTGTAATCCCA | 10580 |
rs755299801 | snp | A/G | 6.4978e-05 | 0.00569954 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336501 | ACGCCAAGTGCACAC[A/G]CGGCATGCTGCAGTC | 10580 |
rs755311147 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345426 | GAGTAATACACACAA[A/G]CCCAACTATACCAGA | 10580 |
rs755321446 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427139 | TTCAAGAATCAGGCA[G/T]TAAGGACTGGAGCCA | 10580 |
rs755332398 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508927 | GAGGTGGGAGTTATT[A/C]ACCAGCGTGGAGGAA | 10580 |
rs755336976 | snp | A/G | 2.57709e-05 | 0.00358954 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341698 | TGACAGAAGGTCAAC[A/G]GCATTTTAGCAGATG | 10580 |
rs755364884 | snp | A/G | 0.000135335 | 0.00822491 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414381 | AGTCATCACACAGGC[A/G]CAGCGGCAGCCAGTG | 10580 |
rs755379449 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525174 | CTGAAGTCCACGAGA[A/C]CTGCCCTGGCAACCA | 10580 |
rs755392817 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397511 | CAGATTTTGAAAACA[C/G]TGGATGAGGATACAC | 10580 |
rs755394078 | in-del | -/T | 1.74885e-05 | 0.00295701 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414871 | GGCATCCTGTGGAAA[-/T]TAAGGGGGTCGTTAT | 10580 |
rs755407861 | snp | C/G | 1.6823e-05 | 0.00290021 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318270 | GGCTCATCGCCCCCT[C/G]TTATTCCCTCAATAC | 10580 |
rs755418726 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95456084 | ATAGACCCAAGTCCA[A/G]TTCAGTTAATGCAAA | 10580 |
rs755443915 | snp | C/G | 3.59893e-05 | 0.00424186 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337051 | CTGACCAACTCAAAT[C/G]GGGGAGGCTGAGAGA | 10580 |
rs755454172 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537309 | CAAGTGTTGGGGGAG[A/G]TGCATGCACACTCAC | 10580 |
rs755492899 | snp | C/T | 3.34024e-05 | 0.00408657 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372081 | GAGGAAATGAAGAAA[C/T]GAGCATAAAGACATA | 10580 |
rs755493727 | snp | A/G | 1.67391e-05 | 0.00289297 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336941 | ACCGTCTCCATTCAT[A/G]TGAAGGGAGGCCTGG | 10580 |
rs755505931 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95497502 | AAAATTCAGACATCC[A/G]TAGCCGTGTCTGACT | 10580 |
rs755536267 | snp | A/G | | | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415907 | ATAAACTGTCCTGGT[A/G]GCTGCATAGCGCTGC | 10580 |
rs755543041 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457251 | CCATGTTGGAAGAAA[A/G]GAACTATGTATTCTA | 10580 |
rs755548072 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545686 | AAACTCCATCTTGAA[-/A]AAAAAAAAAAAGGGA | 10580 |
rs755559388 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540795 | GTAGGAGGTCACTAG[C/T]CATCAGTTCCCTACC | 10580 |
rs755578033 | snp | A/G/T | 3.31001e-05 | 0.00406807 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394641 | TAGGAGTAGATGCAG[A/G/T]AAACTGGTAGGTGGG | 10580 |
rs755585094 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360869 | CCCAGGCTGGAGTGC[A/G]GTGGTGCCATCTTGG | 10580 |
rs755587228 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342885 | TATTATTATTATTTT[-/A]TTTTTTTTTTTTTGA | 10580 |
rs755591290 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524196 | TTCGAAAAAAATGTG[A/T]ATGTTGGGAAAAGGC | 10580 |
rs755593436 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536154 | ACATTGTAAGACAGA[C/T]GTAAAGCAGTTCAGG | 10580 |
rs755597984 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321283 | TTCAATGGCTCCCTA[C/G]TACCTGCAGAATAAA | 10580 |
rs755602583 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374121 | AGCCCCAGTATACAA[A/C]TGGACTGTGTTCTCA | 10580 |
rs755619095 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332088 | AAATCCACCTCAGTG[A/C]GCTCAGTCCTCTCTC | 10580 |
rs755625503 | snp | A/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443167 | GAGCTTACTGAAAAC[A/G]TAGAAGCGGCCGGGT | 10580 |
rs755633646 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467103 | AGTAGGGTGATTTGG[A/G]GTTAACGGTTGTATA | 10580 |
rs755634608 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403972 | CCCTTGTTTCCCATA[C/T]GAGGAAACTGGCTTA | 10580 |
rs755636254 | snp | C/T | | | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415793 | GGAGTTTTCTGACGC[C/T]GCCAGGCAAATGTTA | 10580 |
rs755637736 | snp | C/T | 0.00043422 | 0.0147283 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384348 | GAGAACCAAGTTGTA[C/T]GTTCCCCATTTCCAC | 10580 |
rs755648547 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405570 | CGACAAGCTCTCCAG[C/G]AATTTCTGATGCCTG | 10580 |
rs755664967 | snp | A/G | 3.33884e-05 | 0.00408572 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341531 | TTTGGGCACTGTCAG[A/G]CTTTTCCTTAGAAAG | 10580 |
rs755688533 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322266 | GAAGCACATAAGTCC[A/G]GGGAGAAAACAGAGT | 10580 |
rs755693913 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336755 | AGGGCCTCTTTCGCC[C/T]GCCCCCCTCTCTGCT | 10580 |
rs755697213 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553226 | TCAATAAATAAATAA[A/G]TAAATAGGAACACAT | 10580 |
rs755700769 | snp | C/T | 1.67008e-05 | 0.00288965 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351422 | AATCATCTGTTCCAG[C/T]ATATTAGAAAACTGC | 10580 |
rs755713071 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381484 | GCCACAATAAGAGGG[-/T]TTTTTTAAAAGCAGA | 10580 |
rs755734822 | in-del | -/CATA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318054 | ATAAATAAATAAATA[-/CATA]AATATAAAAAATAAA | 10580 |
rs755745592 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336848 | ATCACTAAGCTGGGA[A/G]ATGACACTATCAGAG | 10580 |
rs755762637 | snp | C/T | 1.65803e-05 | 0.00287922 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95315068 | GTCTTCTTATAGATA[C/T]AAAGGTTTTACATAG | 10580 |
rs755767759 | snp | C/G | 1.70359e-05 | 0.0029185 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371478 | TAGTTTAGAGGAAAG[C/G]GAGAAAGAATGGAAG | 10580 |
rs755787247 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473681 | GAACTACATATAATA[C/T]ATATATACACACACA | 10580 |
rs755788690 | snp | A/G | 1.66153e-05 | 0.00288225 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95371331 | TAGGAAATACCTGTG[A/G]CACGTTTGCACTGGG | 10580 |
rs755791955 | snp | A/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95441437 | CCTTTCAAACATTCT[A/G]TTAAAAACCTCAAGC | 10580 |
rs755805022 | snp | C/T | | | missense | SORBS1 | GRCh38.p7 | 10:95339134 | AGAAGCTTAGATACC[C/T]GTGGGCTTGCAGTGG | 10580 |
rs755812348 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95321482 | GGAAGATATTTTCCT[C/G]CCTTTTCTAGCTCTC | 10580 |
rs755815882 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434679 | CAGGAATGATTTTAA[C/T]AGCAGAAATAGAGCG | 10580 |
rs755824406 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446030 | GGGTAAAAGCCAAAA[-/G]GGACCAACAGTGTAC | 10580 |
rs755847321 | snp | A/C | 1.6941e-05 | 0.00291036 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414844 | CCTCCGGCTGGGCTG[A/C]ACTGGAGGAAGTGGC | 10580 |
rs755857734 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502223 | TGTCAGTAAAATGTG[G/T]CCTAGAAACTCAACC | 10580 |
rs755863597 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360439 | ATGTAAACAAAGTAC[A/C]ATCTAAGAGTATGCT | 10580 |
rs755877478 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433195 | CAGTCTCACTTTCCA[A/G]ACATAACAAAGAAAA | 10580 |
rs755896688 | in-del | -/CA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391510 | CTGAAGCTGTTTCTG[-/CA]CAGTTTGCCCCCTCC | 10580 |
rs755926684 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433975 | TGGACACACAGCCCA[A/G]TTACTTCTGAAAGCG | 10580 |
rs755938685 | snp | A/G | 1.73763e-05 | 0.00294752 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381655 | GAACATGGGCACGGT[A/G]AGACAAAATAACTTT | 10580 |
rs755945915 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95423388 | TAAAATTTTCATGTG[G/T]CATACAATACCATTC | 10580 |
rs755953132 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541933 | CTACACACTCAGGGC[C/G]TAAGCCTGTTGGCCT | 10580 |
rs755972299 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95531329 | CGTCTCCTGGACCCA[A/G]TACGGTTTTCTCACC | 10580 |
rs755983384 | snp | A/T | 1.66941e-05 | 0.00288908 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381812 | TTTCTGCAGAAAGAA[A/T]ATTCTATTAGAGCTA | 10580 |
rs755993942 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390184 | AGAGGTGGCAGTGGC[A/C]ACCACCAGCCTGAAG | 10580 |
rs755994248 | in-del | -/TGTGTG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365171 | TTCATTTACTAACCT[-/TGTGTG]TATGTGTGTGTGTGT | 10580 |
rs756004298 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322174 | AGGTGGCCCCGAGAT[-/A]TCCAGAAACCCCAAT | 10580 |
rs756008234 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543380 | CTCCAGCCTGGGCAA[A/C]AAGAGAGAAACTCTG | 10580 |
rs756013586 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455492 | TTCCCCAAGAGCACA[A/G]TCTTCTCATAACTTT | 10580 |
rs756024297 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491510 | TTTCTGGCTTCTCTT[A/G]AAGAAAGAAAAAAAA | 10580 |
rs756041432 | snp | A/G | 4.94988e-05 | 0.00497463 | missense | SORBS1 | GRCh38.p7 | 10:95339213 | GGTTTTTCACCAGTG[A/G]TCGCTTGATCACATC | 10580 |
rs756045504 | snp | C/T | 2.29345e-05 | 0.00338625 | intron-variant | SORBS1 | GRCh38.p7 | 10:95336489 | CTGCCAAGTGAGACG[C/T]CAAGTGCACACGCGG | 10580 |
rs756059467 | in-del | -/CT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328201 | AACATCATGGGCAAA[-/CT]CTTCCAGAGGAGTAG | 10580 |
rs756064345 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451006 | ACATTTGATATGCAA[C/T]TGTGTAATATTTAGA | 10580 |
rs756064721 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513749 | CCAAGGAGCTTAAGA[A/T]CTCCCTTGGCCACAT | 10580 |
rs756078621 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517372 | ACAAGAGTCGGGTCC[A/G]GCCCTCACCCACTCC | 10580 |
rs756082694 | in-del | -/GAG | 1.65909e-05 | 0.00288013 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315156 | ACACATACAAAACAT[-/GAG]AAGACCCACTCGCTT | 10580 |
rs756083299 | snp | G/T | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95561694 | GGACGCTGGCCTGGC[G/T]CGCCTTCTGGTCCTT | 10580 |
rs756086229 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348977 | GGAAATTGTTAAAAA[C/T]GTAAATTTTCAGGCC | 10580 |
rs756126526 | in-del | -/AGAC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95415295 | ATTTACAGAAAAGAG[-/AGAC]AGACAAAGAGAGTAC | 10580 |
rs756132893 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511580 | TGTTTTTGTCGTTGT[C/T]GTTTCTCAACATCAA | 10580 |
rs756135768 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481012 | GGAATGGCCCAGTAG[A/G]GCATGTGGGGTGGGA | 10580 |
rs756144852 | snp | A/G | 1.64963e-05 | 0.00287192 | missense | SORBS1 | GRCh38.p7 | 10:95381719 | ACGGAAGACTTGCCA[A/G]GCTGATATTCGTAAA | 10580 |
rs756151761 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377537 | TAGGTTGAAATCGGA[A/G]GGAAAATCATACTGA | 10580 |
rs756153047 | snp | C/T | 1.65288e-05 | 0.00287474 | missense | SORBS1 | GRCh38.p7 | 10:95432468 | TTGCTTTCGTGTTGC[C/T]GGGTTTCCTGAGGGC | 10580 |
rs756155462 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418632 | CTCCTGACCTCAGGC[A/G]ATCCACCCACCTCAG | 10580 |
rs756168228 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95551271 | GATTGAGTGAAAGTC[C/T]GCATATCAAACAGAC | 10580 |
rs756171962 | snp | A/C | 2.79943e-05 | 0.00374117 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422240 | GGTGCAGAAAGGATG[A/C]AAACAAGAAAAGGGG | 10580 |
rs756174974 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95368240 | ATTTAGATAACTTGT[G/T]TATGCCTGCAAATTT | 10580 |
rs756176635 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382430 | CTGTTCCACACTGGA[A/C]TAGGGAAGAGGTAAC | 10580 |
rs756200096 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499601 | CCAGTTGCATGCACT[A/G]GTTTTTCTCTTACAA | 10580 |
rs756223586 | snp | G/T | 0.000288642 | 0.0120099 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357150 | ACCCATTAGGTTAAA[G/T]CTGAAAGCTGCTAAA | 10580 |
rs756234232 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435225 | GGGTCTTGTGCCTGC[-/T]CCGATAATTGTAGCC | 10580 |
rs756239480 | snp | A/T | 1.77259e-05 | 0.00297702 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336550 | TCCGAGCAGCTTTCC[A/T]CCCCGCCTGCTCGCC | 10580 |
rs756290580 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489263 | CTTTTTCTCTCTCAC[A/G]TACATAGAAGCCTTT | 10580 |
rs756298895 | snp | G/T | 3.31153e-05 | 0.00406898 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95394647 | TAGATGCAGGAAACT[G/T]GTAGGTGGGAGTGTA | 10580 |
rs756299899 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528658 | GCGCAGTGGCTCACG[C/T]CTCTAATCCCAGCAC | 10580 |
rs756322549 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500653 | TACTTTTTTAACGTG[C/G]CTACTAGAAAGTCTT | 10580 |
rs756328014 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471543 | GGAAACATAGTGAGA[A/C]CCCATCTCTACGAAA | 10580 |
rs756328405 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498845 | TTCTTGATTATGGTG[A/G]TCATTATACAAATCT | 10580 |
rs756342154 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411464 | TTATTAATACTAACA[C/T]TATAATCTGCATATT | 10580 |
rs756344437 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407534 | TGAGGCATGAGAATT[A/C]CTTGAACCTGGGAGG | 10580 |
rs756346043 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489999 | AAAGAGTAGCTCAAA[G/T]AAAGATGCATGGGTT | 10580 |
rs756352918 | snp | C/G | 3.37923e-05 | 0.00411036 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336953 | CATGTGAAGGGAGGC[C/G]TGGGAAGTAGGTGCT | 10580 |
rs756378052 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449966 | AAATATTTTTAGATA[C/T]GTGAAGAAATGATTC | 10580 |
rs756382857 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524838 | CTGGCACATAATGGG[C/T]ACATAATAAACATCT | 10580 |
rs756388346 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95366999 | ACACCAGATGTGGCC[C/T]GTCTCAGTCACACTC | 10580 |
rs756393378 | snp | A/G | 3.38995e-05 | 0.00411686 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351166 | GGCAAATAGGCAAAT[A/G]TTGCTTTGGGTCAAG | 10580 |
rs756396019 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557714 | CTCTCAGTCCACCCC[C/T]CCACCCCCCATCCTA | 10580 |
rs756398309 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516941 | GAGATAGTTGTTGGA[-/T]TCCCCAGGTCAAGCC | 10580 |
rs756398782 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95421144 | TGCACTCTGGCCTGG[A/G]CAACAGATAGAGACC | 10580 |
rs756409795 | snp | C/T | 1.65149e-05 | 0.00287353 | missense | SORBS1 | GRCh38.p7 | 10:95357732 | ATTTGTCTCTCATTC[C/T]CCAAGCTAGTGAGAT | 10580 |
rs756414507 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519519 | ATGTATGGCAGGGTA[C/T]GGAGGAAATGGCCAA | 10580 |
rs756417775 | snp | A/G | 3.48949e-05 | 0.00417687 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341719 | TTAGCAGATGTTTCA[A/G]TATGTGTAAGATTAA | 10580 |
rs756421748 | snp | A/G | 1.65403e-05 | 0.00287574 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394969 | TTAATTTAAAGCTCG[A/G]ACAACAGATATGCTG | 10580 |
rs756427041 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95529605 | AAAGGCACTGCCCCA[C/T]AAGGACTCCATATTT | 10580 |
rs756443842 | in-del | -/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358706 | CACATGCACAGACAT[-/GC]GCGCGCGCGCGCGCG | 10580 |
rs756445785 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358134 | GGATAGGGGAGAACA[-/G]GGGGAGGATCACACA | 10580 |
rs756466725 | in-del | -/ATA | 1.65446e-05 | 0.00287612 | cds-indel, intron-variant | SORBS1 | GRCh38.p7 | 10:95372026 | GCAGTCTCCAGGAGT[-/ATA]ATCCCATATCTTTTT | 10580 |
rs756501194 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526457 | CAATGTGCAGGCAAG[C/G]CTGAGAATTATTGCT | 10580 |
rs756510121 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334617 | CTGCCTTAGGAAGCA[A/G]GAAGCGTATACCCCT | 10580 |
rs756521759 | in-del | -/AACATAG | 1.64985e-05 | 0.0028721 | splice-acceptor-variant | SORBS1 | GRCh38.p7 | 10:95410777 | TAGAGGACTGGAATC[-/AACATAG]CTGAAACGAACAAAC | 10580 |
rs756549950 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512008 | CCTAGATGCTAGACA[-/C]CATGTTAAAAGAGCT | 10580 |
rs756558229 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465396 | AGCCGGATGTGGTGG[C/T]GAGTGCCTGTAGTCC | 10580 |
rs756565814 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325949 | TCACCTCGGACTCTG[A/G]CAGGGGTAAAGGAAG | 10580 |
rs756580043 | snp | C/G | 1.65222e-05 | 0.00287417 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321926 | GACCAACAGTCCTCT[C/G]AGAACATGAGAATCG | 10580 |
rs756605275 | snp | C/G | 1.64844e-05 | 0.00287087 | missense | SORBS1 | GRCh38.p7 | 10:95318384 | ATCGCGGAGTTCCAA[C/G]TCATCATCATTCTGT | 10580 |
rs756609144 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455105 | TACTAGATGTGTCTT[C/T]TGTGGTTAGTCAGTT | 10580 |
rs756617281 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355564 | GGCACAGAGGAGGAC[A/G]GGATAATGCAAGCAA | 10580 |
rs756633867 | snp | G/T | 3.30956e-05 | 0.00406776 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394959 | ACTATAAGAATTAAT[G/T]TAAAGCTCGGACAAC | 10580 |
rs756647146 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507357 | CCACCACTCAGAAAG[C/T]CTGTTCTTAACCATT | 10580 |
rs756651841 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496409 | TTCCTGGGTGCTCAA[C/T]GATGAGGTCGCTCCC | 10580 |
rs756666968 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426979 | TTTAATGGAGGTACG[A/G]GGTACCTTCAACTGC | 10580 |
rs756670472 | snp | C/T | 1.7886e-05 | 0.00299044 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337117 | GGTCAGTGTTATAGA[C/T]AGAAGCCTCTGGCAG | 10580 |
rs756671682 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345272 | ATTGAGTGGGGGAGA[A/C]GTTGATAACTTCACT | 10580 |
rs756676924 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535225 | GAAGAGACCACTTCA[G/T]CCAAAGTGCCTAGTA | 10580 |
rs756698879 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547282 | CCTGCACCTCCACAC[A/G]CACTGTATCATACTA | 10580 |
rs756699207 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425022 | ACACCTGGTGACATG[C/G]CATGACAATGGTCCA | 10580 |
rs756713105 | snp | A/G | 1.7024e-05 | 0.00291749 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434758 | GCATCCAGAAAGAAC[A/G]TTTGGGAAACACTCA | 10580 |
rs756722571 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562648 | CAGGCTGTGGGTGGC[A/G]GGGTAAAGACTGGCC | 10580 |
rs756724605 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344210 | CTACCATGGGAAACC[C/T]GGGGCCCCATTCTTC | 10580 |
rs756728970 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426844 | CCTGAGAGTGGTTTT[A/G]TGAATCCCCTGAACT | 10580 |
rs756736670 | snp | G/T | 0.000110357 | 0.0074274 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415903 | TATGATAAACTGTCC[G/T]GGTGGCTGCATAGCG | 10580 |
rs756739820 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95546057 | GGCCTTTCATACTAG[A/G]AAACCGAGGTCAGCC | 10580 |
rs756746716 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425897 | AGACTGTCAAAATGC[G/T]TCTTTCAATAAATGT | 10580 |
rs756753602 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399952 | TGTGGACATGAAGGT[-/G]AGCATTCCAGAATCT | 10580 |
rs756757325 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453627 | ACAGGCATGAGCCAC[C/T]GTGCCCAGCCCATTA | 10580 |
rs756757849 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507195 | CATCTTTATCAAGAC[C/T]CAAATACAGTTAGAA | 10580 |
rs756763390 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465181 | AATTTTAACACGGTG[C/T]CTTGGATGAAGTAAA | 10580 |
rs756765120 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95448626 | GAGACCAACATGATC[-/A]GACAGGATTGCTGTC | 10580 |
rs756765744 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513281 | CACCCTTGACTGGTA[C/T]GGCATTTCAGAGCAT | 10580 |
rs756773502 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95344054 | CACCCCTATGGAGAT[C/G]TGCAGGCTCCTGATT | 10580 |
rs756775765 | snp | C/T | 1.66241e-05 | 0.00288302 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371953 | GCTAGAGAGCACACA[C/T]AGTCCAACGGAGGAG | 10580 |
rs756779446 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505892 | CTTGTTATCCCATCG[A/G]CAGACTGAGAATGAA | 10580 |
rs756789019 | in-del | -/AAGAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362929 | TAATTTAGTTATTTC[-/AAGAAG]AAGAAGAAGAAAAAA | 10580 |
rs756792842 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535112 | ATGAGTAGATGGATA[C/G]AGATGCCCAGGAATT | 10580 |
rs756801605 | snp | A/G | 1.65018e-05 | 0.00287239 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95434691 | TAACAGCAGAAATAG[A/G]GCGTGCGCGTAAAGG | 10580 |
rs756801731 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413355 | CACAAAGCTTGAGAA[A/G]TGACCTCCTACTCCA | 10580 |
rs756806722 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524094 | AGGAAAGTGGGTGAT[A/C]CTGATATCTACAAAT | 10580 |
rs756807571 | snp | A/C | 1.66358e-05 | 0.00288402 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336933 | TGGACACCACCGTCT[A/C]CATTCATGTGAAGGG | 10580 |
rs756819164 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95496222 | GCCACCGTGCCCCAC[C/T]ATGGGCAGTGTTTTT | 10580 |
rs756839453 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331840 | GAAGTAATTAGACTT[C/T]CCTATCATTTAAAGC | 10580 |
rs756849990 | snp | A/G | 1.74943e-05 | 0.00295751 | stop-gained | SORBS1 | GRCh38.p7 | 10:95339135 | GAAGCTTAGATACCT[A/G]TGGGCTTGCAGTGGC | 10580 |
rs756882801 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318856 | ATGAAACCATCAGGA[C/T]ATTAGTTAGATTCTC | 10580 |
rs756890616 | snp | C/T | 1.66715e-05 | 0.00288712 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315169 | ATGAGAAGACCCACT[C/T]GCTTGAGTTGAGACA | 10580 |
rs756896716 | snp | A/G | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443034 | TACATACCTCGACTA[A/G]TAAGGTCTTACTGAA | 10580 |
rs756901939 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320222 | CCCCACTTCTGGAGA[G/T]GGAAGCTTGCTGTGG | 10580 |
rs756906835 | snp | A/T | 1.72764e-05 | 0.00293903 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414861 | CTGGAGGAAGTGGCA[A/T]CCTGTGGAAATAAGG | 10580 |
rs756908359 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95402506 | GAAGTGCAGTGGCAT[A/G]ATCATGGCTCACTGC | 10580 |
rs756915496 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95484957 | CCAGCCGGGACAACA[G/T]TGCGAGACCCTGTCT | 10580 |
rs756953916 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431738 | GCTGACAGGTGGTGG[C/G]GACAGGGTGTGCACA | 10580 |
rs756967862 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376555 | TGCCTTAAGGTTTTC[A/G]AAATAAACACAAATA | 10580 |
rs756971808 | snp | A/G | 1.65957e-05 | 0.00288055 | intron-variant | SORBS1 | GRCh38.p7 | 10:95372055 | TTTTGGGAGGCTGAC[A/G]GGAAGCAGAGGAGGA | 10580 |
rs756977977 | snp | C/T | 1.67657e-05 | 0.00289527 | missense | SORBS1 | GRCh38.p7 | 10:95354944 | AGTAATCAGCTGGTA[C/T]AAAATGTCTTGGCGA | 10580 |
rs756987432 | snp | C/T | 1.65679e-05 | 0.00287814 | splice-acceptor-variant | SORBS1 | GRCh38.p7 | 10:95399190 | TTTCTGAGACAGGAT[C/T]TGGAAATGAAAAGCA | 10580 |
rs756993331 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474294 | GAAATGGGTATGTCA[C/G]CTCCATGCCACCAAA | 10580 |
rs757000933 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95552375 | CCACTGCACTCCAGC[C/T]TGGGCAACAGAGTGA | 10580 |
rs757001855 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95465022 | TTTCAACACAGCACC[A/G]TTTCCCCCAAAGGAT | 10580 |
rs757004495 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345051 | TCTTACAAAGACTCC[C/T]CAATTCAAAGAAATA | 10580 |
rs757016635 | snp | C/T | 1.68451e-05 | 0.00290211 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381831 | CTATTAGAGCTATTT[C/T]CATGACAACTGGCAT | 10580 |
rs757023735 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339653 | CTTCATTTCTAAGGC[-/A]AAGATTTTGGGGGGT | 10580 |
rs757026852 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443965 | CTCATGTTTTCCAGT[C/T]CTAAGTTTTTGATAC | 10580 |
rs757072127 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466813 | TTTTTTTTTTTTTTT[-/C]TAAGAAAAAATAATC | 10580 |
rs757074335 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524843 | ACATAATGGGCACAT[A/G]ATAAACATCTGGTGA | 10580 |
rs757074360 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95530266 | ACCAGACACAACCAG[C/G]TGTTCCTTCCTACCT | 10580 |
rs757074673 | snp | C/T | 8.25948e-05 | 0.00642577 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336632 | CAGGGGCTTGCCGGG[C/T]CGGCTCTCCTCAGGG | 10580 |
rs757076033 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432907 | TAGGTTGATGAGCAG[A/G]CTTCTGACCAGTTAG | 10580 |
rs757094003 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390708 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 10580 |
rs757102818 | snp | C/G | 0.000185684 | 0.00963366 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415719 | AGGCCGGGAGCCGGT[C/G]CTCGGGTGCCCGCAG | 10580 |
rs757107888 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95472933 | GCTAATCAGGAGGCT[A/G]AGGCGGAGAATTGCT | 10580 |
rs757118935 | snp | A/G | 6.59761e-05 | 0.00574314 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95339232 | CTTGATCACATCCAC[A/G]TAGGTGATGGGGAAG | 10580 |
rs757121687 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95357758 | GAGATCCCCAGGAGC[C/T]CCGTCTGATTCCCTC | 10580 |
rs757143247 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95389539 | TGACCTCCTGAGTAG[C/G]TGGGATTACAGATGT | 10580 |
rs757155488 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95500874 | CAGGCATAACATCCA[C/T]ACCCTGGGCTGCTGC | 10580 |
rs757167130 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473566 | CTGGGAGGTGGAGGT[C/T]GCAGTGAGCCAAAAT | 10580 |
rs757200832 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460930 | TAATTATTGAACTAA[A/G]TATTAGTTATAATCC | 10580 |
rs757201157 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95541833 | CCTCCTATTGGTCCT[C/T]CAAGGCTCTGTCCAA | 10580 |
rs757210555 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502135 | TGTGCTAAACCACCT[C/G]CACCTCAAAGCAGTA | 10580 |
rs757233883 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440554 | CTGCATGATGAGCAG[A/G]GATCTGTTCCCATCT | 10580 |
rs757234093 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549084 | CTAATCATAAATGTC[A/G]GGTCTAGAAACACAG | 10580 |
rs757234270 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95482854 | GAGACAGCAGGTTGC[C/T]GTAGAGTTGGTGGCA | 10580 |
rs757240129 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357989 | AGACATTTCTACAGA[C/T]AGGCCCATGGAGCCC | 10580 |
rs757243568 | snp | C/T | 3.4805e-05 | 0.00417149 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336557 | AGCTTTCCTCCCCGC[C/T]TGCTCGCCACCTCTA | 10580 |
rs757245895 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450410 | GTTGAACAGTTATGA[C/G]AATAACTAACATAGA | 10580 |
rs757248270 | snp | A/C | 1.68684e-05 | 0.00290412 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351185 | CTTTGGGTCAAGCAG[A/C]AGATTGAGGTGACCA | 10580 |
rs757250862 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | SORBS1 | GRCh38.p7 | 10:95384030 | CGGGCTGGGAGGGGT[A/G]GTGTGGCCGACCTCT | 10580 |
rs757263951 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95491330 | CCATTAGAATCACAG[C/G]ATCTTGGGCAGAAGG | 10580 |
rs757277541 | snp | A/G | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562863 | GAGCCCCCAGCCCAC[A/G]GCCTTCCCCTATCTG | 10580 |
rs757281103 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521894 | GAATTGCTGAGCTCA[A/G]GTGATCCCCTTGCCT | 10580 |
rs757284709 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95380020 | TTGGCCTGCCTTTGG[A/T]GTTCATGCCCCATTA | 10580 |
rs757285681 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95518559 | AGGATGCTGTTGAGC[-/A]CACAAAAACACGTGC | 10580 |
rs757290757 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509000 | AATTTGGAGGTGACT[-/G]GGGGTGGCCCTGGGA | 10580 |
rs757291197 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537742 | GTGCTGCTTCACCTG[A/C]GGTCACACAGCTAGT | 10580 |
rs757292797 | snp | C/T | 1.82327e-05 | 0.00301927 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414566 | GGCAGGAGGGACCAG[C/T]GGAGGTGGTGGTGAG | 10580 |
rs757297818 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95538113 | TGAGACTTTGTCTCC[-/A]AAAAAAAAAAAAGGT | 10580 |
rs757304089 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386464 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 10580 |
rs757304633 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337770 | TCTCTGGGAGCTCAG[C/T]AGAGTCTTCCAGAGA | 10580 |
rs757314886 | snp | A/G | 1.84252e-05 | 0.00303517 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414515 | CGAAACAGCTCCCGT[A/G]AGGTCAGGCTCCGAG | 10580 |
rs757323359 | snp | A/T | 2.04882e-05 | 0.00320058 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357848 | AGAAAAGGGAAAAAA[A/T]AAAGATAAGAATAGG | 10580 |
rs757328455 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391854 | TAGAATTTAGACAGA[A/G]ATGGCAGCCCTTAGG | 10580 |
rs757340365 | in-del | -/CTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527680 | GGCACTCTATGAATC[-/CTT]CTTGACTACTGGTCA | 10580 |
rs757346807 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328570 | GGTAATGGCAGATAC[A/G]TATTCAAGTGTGAAG | 10580 |
rs757363212 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95455838 | ACTCAGGAGGCTGAC[A/G]CAGGGGGACTGATTT | 10580 |
rs757364597 | snp | C/T | 0.000120999 | 0.00777722 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356904 | GAGGGCAAGAGGATA[C/T]TCTTCTGTTCCTGCA | 10580 |
rs757377149 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95510091 | CCTTTTCTGATTAAA[C/G]TAATACTGTTCACTG | 10580 |
rs757408845 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95345952 | TAAGATTTTAATCTC[C/T]TGGGATGTTGTAGCA | 10580 |
rs757411205 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95543332 | TGAACCTGGGAGGCG[-/A]AGGTTGCAGTGAGCT | 10580 |
rs757414320 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369400 | ATCTTAAGCCCATGC[C/T]TCTTCCAAGAACTCT | 10580 |
rs757422559 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556612 | TGGGGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 10580 |
rs757431022 | snp | A/G | 0.000263639 | 0.0114782 | missense | SORBS1 | GRCh38.p7 | 10:95432529 | AGGAAGACGAGGCCC[A/G]GAGAGTCACCGCTCC | 10580 |
rs757438559 | snp | A/G | 1.66394e-05 | 0.00288434 | intron-variant | SORBS1 | GRCh38.p7 | 10:95376071 | TCTATAGGGGTTGGT[A/G]ATAGAGAAATGGAAG | 10580 |
rs757463954 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330515 | TTTTTTTGTTTACTT[C/T]TTAAAATTTTTTTGA | 10580 |
rs757471525 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316858 | TTAGAATTAATTTCA[C/T]TGGTTTCTTTTTACT | 10580 |
rs757474193 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515865 | CCTAACGCACCCTAT[G/T]AGAGAGGTACCTTCT | 10580 |
rs757475263 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499496 | GATAACAACTGGATG[A/G]AGCCGGGTAGTAGCT | 10580 |
rs757482876 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95470412 | CAAAAATTCACAGCA[A/G]AACACTTAATGCAAA | 10580 |
rs757498285 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434952 | CTGGTCAGTGTTGAC[C/T]GGTGCCTCCTACCAC | 10580 |
rs757498963 | snp | C/T | 1.6517e-05 | 0.00287372 | missense | SORBS1 | GRCh38.p7 | 10:95422007 | ACACTTCTGTAGCCC[C/T]TGGCAGCGAGTGAAG | 10580 |
rs757500403 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509620 | AGGATTTTTCTTCCT[-/C]AAAAAAAAAGAAGAA | 10580 |
rs757505205 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488210 | AGGCTGCTGGATGTT[C/T]CTGCTTGCTAATAAT | 10580 |
rs757529776 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371846 | TTTTATTACCTAACC[-/A]AAAAAAAAAAAAGCA | 10580 |
rs757532641 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458792 | TCTCACTGTTTAAAT[C/T]TATATCTTGAATATC | 10580 |
rs757549407 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335702 | ACTAGACTGTAAGAG[G/T]TGGAGCTGGCATTCA | 10580 |
rs757549827 | snp | C/T | 1.77027e-05 | 0.00297507 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337139 | CTCTGGCAGAGGAGG[C/T]AAGGGTGGGGTCAGG | 10580 |
rs757550966 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430168 | AAAGTGCCTCAAATC[C/T]ACACACGGGGCCGGG | 10580 |
rs757559374 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446737 | CTCTGTTTAACCTTC[A/G]GAACCTAACTTCAGA | 10580 |
rs757566467 | snp | C/T | 1.79978e-05 | 0.00299976 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337077 | AGAGACAGGGAGGGA[C/T]TGGCCCTTGGTGACA | 10580 |
rs757567682 | snp | C/T | 1.78172e-05 | 0.00298468 | intron-variant | SORBS1 | GRCh38.p7 | 10:95377338 | GCTCTTCTTGTACTT[C/T]ACTTACAACACAGTT | 10580 |
rs757604053 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364822 | TTATTACAAAATTTT[A/G]AATCAGTATGGGGCA | 10580 |
rs757607031 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417307 | TTTTCTTTTGTTTTG[C/T]TTTATTTTGTTTCGA | 10580 |
rs757634439 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395560 | ATTAAGAACTATAAC[A/G]TGAGAACACCAAAGC | 10580 |
rs757640418 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505094 | TTCCCTCCCTTTGGT[A/G]TTCAACAAGAGATCC | 10580 |
rs757653067 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377199 | GAAATATAAAATGCA[C/T]ACACTTTCTACTGAG | 10580 |
rs757675491 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406595 | TAGCGCTTTTGCAAA[C/T]AACACTTGTAAACTT | 10580 |
rs757677018 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476872 | ATCTTTAATAATGGA[A/G]TTAAGGTGCTTTTCT | 10580 |
rs757677818 | in-del | -/G | 1.76538e-05 | 0.00297096 | frameshift-variant, intron-variant | SORBS1 | GRCh38.p7 | 10:95337146 | AGAGGAGGCAAGGGT[-/G]GGGTCAGGGCCAGAG | 10580 |
rs757683197 | snp | A/C | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312786 | TCAAAATTCCCTACT[A/C]ATCAAGAAGCACCCC | 10580 |
rs757711139 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353041 | CCCTGTAGTTTAACC[A/G]TATAAGCCAAAAACC | 10580 |
rs757723389 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528467 | GATATAAAGGGGTCA[A/T]CCTGAGAATGGTTCT | 10580 |
rs757747928 | snp | A/C | 1.65141e-05 | 0.00287346 | intron-variant | SORBS1 | GRCh38.p7 | 10:95321940 | TGAGAACATGAGAAT[A/C]GAAGTTCACCAGGAG | 10580 |
rs757749416 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480636 | CTAGCTGATCTTGTA[C/G]GTGTCTTTCAGCTCT | 10580 |
rs757769587 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | SORBS1 | GRCh38.p7 | 10:95341344 | ACTTAGCAATAGCTT[C/T]TCCATATTCCAAAAC | 10580 |
rs757808466 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95477524 | AAGTTTTTGGAAGGG[A/C]AAATGAGGAGTCAGA | 10580 |
rs757809062 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436744 | GGCAGATCATAAATT[A/C]CCTCATCTTATAGAT | 10580 |
rs757809606 | snp | C/G | 1.64751e-05 | 0.00287007 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95410682 | GACAATCGTTGTGGA[C/G]GGATAGGCGGATGAA | 10580 |
rs757809958 | snp | C/T | 1.65553e-05 | 0.00287705 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95376039 | TAAATCTATCTCTTC[C/T]GGGCTTATATCCCGA | 10580 |
rs757815277 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434162 | CTGGGATGGCCCGGT[-/G]GAGCATCAGAGGCGA | 10580 |
rs757823052 | in-del | -/AAGTA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95418573 | TTTTGTATTTTTTTT[-/AAGTA]AAGACAGGGTTTCAC | 10580 |
rs757829237 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545014 | ACTAATGTACCACGT[C/T]CAACATAGAGGCCCT | 10580 |
rs757844990 | snp | A/C | 1.77552e-05 | 0.00297948 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422107 | AAAATCTCTCACTCA[A/C]AGGGAATAACTCCCT | 10580 |
rs757873823 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435600 | TCTCTTTCAAGGGCA[G/T]CACATAAAGAGGGAT | 10580 |
rs757874257 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382599 | CCAATGTATGTTCTT[A/G]GCACCTTTGTGGAAA | 10580 |
rs757876547 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95395372 | TTACTTTTGATAGGC[A/G]AGAAATATTAAGTAT | 10580 |
rs757877272 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544875 | TGCAGGCTGGCGGCT[A/G]CAGACCCTCCTCCCG | 10580 |
rs757884414 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95557230 | GTTAGTGCTCTGGTC[A/C]ACCACTGTTCACAGC | 10580 |
rs757891292 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95353785 | TGCTGGGATTACAGG[C/T]TTGAGCCACTGCACC | 10580 |
rs757918446 | in-del | -/CT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95318268 | ATGGCTCATCGCCCC[-/CT]GTTATTCCCTCAATA | 10580 |
rs757919264 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95360524 | CCCAGGCTGCCAACT[A/G]ATCAGCCCACATCTA | 10580 |
rs757924738 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516628 | AAAGCGCACAAAAAT[C/T]AGAGACTTAACTCTA | 10580 |
rs757928488 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533943 | AGAAGAAGATAAAAG[A/C]AGGAGCTGGCTGAGC | 10580 |
rs757929683 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95394305 | TCAGGTGACCACCTC[A/G]GGTACAAAGCCTTGG | 10580 |
rs757938082 | snp | A/G | 0.000133378 | 0.00816524 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355700 | TGAGTATGGCACGGA[A/G]TTTCCATTATTAATG | 10580 |
rs757938856 | in-del | -/TTTTTAAAGCAATTAAAA | 1.70075e-05 | 0.00291607 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371294 | CACAGCTTGAAAAGG[-/TTTTTAAAGCAATTAAAA]AACTGATGGCATGAG | 10580 |
rs757951475 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407292 | ATTCACTAAACCTCT[C/T]GGCCTCAGTTTCCTT | 10580 |
rs757955763 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533077 | AAACCCTGGGTCTTG[C/G]GGGTAATAGCGCAGG | 10580 |
rs757956183 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504992 | AAGGGAGTTTCTAGA[A/G]GAGCAGCTGCCGTCG | 10580 |
rs757957966 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95318372 | AACGATATCTCCATC[A/G]CGGAGTTCCAACTCA | 10580 |
rs757977624 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95343720 | TGTAACTTGGAAGGG[A/G]TGTGCTCACTTTGCA | 10580 |
rs758009301 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95505812 | CTGGGAACAACAGTT[C/G]CCATGGCAGCCCTGG | 10580 |
rs758022332 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95453103 | CCAGCCTGGACAACA[C/T]GGTGAAACCCTGTCT | 10580 |
rs758023539 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95339586 | TTGTGTCCCTAAGCC[A/C]GGGAACAAATGTAGT | 10580 |
rs758041066 | snp | C/T | 5.07679e-05 | 0.00503799 | intron-variant | SORBS1 | GRCh38.p7 | 10:95399224 | GTTAGCTGAAGCTCT[C/T]TTGGTAGCTGCAAAA | 10580 |
rs758041221 | snp | G/T | 1.65619e-05 | 0.00287762 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406168 | ATAAAAGAACACACA[G/T]TGTAAGTAAGATTTA | 10580 |
rs758058656 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399899 | TCTGGCTTCCAAGCT[A/G]TGACATTTATTTATT | 10580 |
rs758112971 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342339 | CTGAACTTGGAGCTA[A/T]CTCAGAGTTGCTGGA | 10580 |
rs758115874 | snp | A/G | 1.74552e-05 | 0.0029542 | intron-variant | SORBS1 | GRCh38.p7 | 10:95339337 | CTCACCCTGGAAGAC[A/G]CAGCAAAGAGAGGGT | 10580 |
rs758125678 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95330143 | CCCCAAACTACTGGC[C/T]TAGAGTCCTTGGCTG | 10580 |
rs758126338 | snp | C/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312690 | GAATTTCTGGAGATA[C/T]ACAAATGCGTGAGGC | 10580 |
rs758131396 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95485426 | AAAGTTCAACAAGCA[C/T]AAATAATACAATCAT | 10580 |
rs758132968 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95370696 | TCTCTTACTCTCTCT[C/T]GTATACCCTTTAATA | 10580 |
rs758134029 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442113 | CTGATCTGCTTTCTG[C/T]TACTATTGTTTTACC | 10580 |
rs758134390 | snp | A/G | 0.00013796 | 0.00830426 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355865 | ATGGGGCTGACTGGG[A/G]AGGTCTGGCTTCTGG | 10580 |
rs758144151 | snp | C/T | 3.31669e-05 | 0.00407215 | missense | SORBS1 | GRCh38.p7 | 10:95357762 | TCCCCAGGAGCCCCG[C/T]CTGATTCCCTCTTCA | 10580 |
rs758206993 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534992 | TCAACATCTCGTTCA[C/T]CCTCACATATCTAGC | 10580 |
rs758217422 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347968 | ATTCCTGGGTTCAAG[C/T]GGTCCTCCTGCCTTG | 10580 |
rs758234636 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413208 | GACCCCAGCATCTGA[A/G]ACCCCTGAGCACTTG | 10580 |
rs758245536 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447160 | ACAAAAACAAACAAA[A/C]AAAAAAAAACAAAAA | 10580 |
rs758245686 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95408283 | ACTCTCAGGATCCGA[C/T]GCACATAGACTGAGA | 10580 |
rs758259401 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523265 | CGCCCAAGACTAGAC[C/T]ACTCCCAGGGCTAGG | 10580 |
rs758262053 | snp | G/T | 1.65141e-05 | 0.00287346 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336635 | GGGCTTGCCGGGCCG[G/T]CTCTCCTCAGGGGTG | 10580 |
rs758270807 | in-del | -/AAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383417 | CAAAACTCCGTCTCA[-/AAAAA]AAAAAAAAAAAACTC | 10580 |
rs758287140 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457127 | GGAATAAAAGGTGAC[-/A]AGAGTTAGGGATGTT | 10580 |
rs758294550 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336732 | TTCTTAGAGATCTTG[A/G]GTCCACCAGGGCCTC | 10580 |
rs758314141 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95511885 | CTTCCTCCAGCCCTC[A/T]AAGAAGGGCCTTCTC | 10580 |
rs758314740 | snp | G/T | 1.6612e-05 | 0.00288196 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434577 | AGGAAAACCATGCCA[G/T]GATCCGCTCACAGTT | 10580 |
rs758323670 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471623 | GCTACTTGGGAGGCT[A/G]AGCAGGAAGATCAGC | 10580 |
rs758328286 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430493 | AACAAATCCACACAC[A/G]GTACTGGTAGCACAG | 10580 |
rs758332189 | snp | A/G | 1.94748e-05 | 0.00312042 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367612 | TTTCTGACATTTAAC[A/G]TAGTAAGCAATGTAA | 10580 |
rs758347231 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512906 | AGTAAATTTCCAAAC[A/G]GTAAGATTTCCACAA | 10580 |
rs758347743 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450930 | ATTTTCTAAACTGTT[G/T]ATAATGTGCTTATAA | 10580 |
rs758354363 | snp | C/T | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95443016 | TTCAAAGTACAAGTC[C/T]TGTACATACCTCGAC | 10580 |
rs758359756 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331723 | CTTGGTGACCATCCA[G/T]CAAGCCCCAGAGGCA | 10580 |
rs758361735 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559863 | GTCTGAAGGCTGTAG[A/G]TATGTCCATCATCTG | 10580 |
rs758369817 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95368133 | CCCAATGCAGAGCCC[C/T]TCATGCACCCCAAAT | 10580 |
rs758385686 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95539668 | ACCTACCTCATGGGG[A/G]AGCGATGGCAGTTAC | 10580 |
rs758390775 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95397599 | TATATAGACTGTGCC[A/T]AACTGAAGGAAAGTC | 10580 |
rs758392937 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554906 | TTTTTTTTGAGATGG[A/G]GTTTCGCTCTTGTTA | 10580 |
rs758396001 | in-del | -/ACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95471316 | GGTAGGATGCTATTG[-/ACA]ACAATTGAGCTGTAA | 10580 |
rs758419603 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381577 | TCATTATCTTCAAAA[A/C]AAAGTTAAGTCTATC | 10580 |
rs758426951 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537943 | GGCAACATGGCGAAA[-/C]CCCCATCTCTCCAAA | 10580 |
rs758429554 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459683 | GGGGAAACCCTTCCG[C/T]GGCCCCTCAGCTCTG | 10580 |
rs758445052 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95519037 | TTCCCTCACTTCAAC[C/T]CCTGCACTGCTGTAC | 10580 |
rs758446171 | snp | C/G | 8.79206e-05 | 0.00662967 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337153 | GCAAGGGTGGGGTCA[C/G]GGCCAGAGAACGCCT | 10580 |
rs758462372 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95479861 | ATTTCTAGATGGCCG[C/T]CTTGTATGCCATCTT | 10580 |
rs758490563 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95395074 | GTTTTCTTCAGGAGT[A/G]TCTAGGCAGAGGAGC | 10580 |
rs758492544 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95438433 | GACAGGCCAGTCTGG[A/G]TGCTGCCTGTGGGCC | 10580 |
rs758498788 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95503559 | TGGGCCTAGCACCAT[A/G]AAGAACTTCTAAAAT | 10580 |
rs758506729 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95410283 | AAAGAGGTATTATTG[C/T]ACCTAGATTTTCGAA | 10580 |
rs758520194 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95553031 | ACCAGCCTAGGCAAT[A/G]TAGTGAAACCCCATC | 10580 |
rs758534605 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387831 | TGGCCAGGCCAATTT[C/G]CAGCCCCTGAAGCCT | 10580 |
rs758540833 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | SORBS1 | GRCh38.p7 | 10:95351383 | TAAAAGTTTCTGCCA[C/T]AAAATTGCATAAAAT | 10580 |
rs758553426 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521743 | GCTCACTGCAGCTCA[A/G]CCTCTGGGGCTCAAG | 10580 |
rs758578536 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315243 | CTGCAGCTTAGAGAA[C/T]ACCGTATGGTTTCCA | 10580 |
rs758581523 | snp | A/G | 1.66751e-05 | 0.00288744 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414647 | TGGCTGGCTGTGGTG[A/G]GGCCACCTCTGCAGA | 10580 |
rs758582144 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95508825 | TCATTCCTCATTAAT[A/G]AGAAAGATGTTAAGC | 10580 |
rs758590732 | in-del | -/TT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554886 | TCTTTTTTTGTTTGT[-/TT]TTTTTTTTTTTGAGA | 10580 |
rs758598961 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390569 | GGAAGAGTGGTATTT[-/C]CCCATCCCAGTGGTT | 10580 |
rs758614601 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480808 | ATGCGAGAGACTTAC[A/C]AATGAGTCTGTACAG | 10580 |
rs758624672 | snp | A/G | 1.65081e-05 | 0.00287293 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322069 | AAGGGGATACCTTGT[A/G]ATGAAAGTCAAGGGG | 10580 |
rs758627089 | snp | C/T | 0.000484731 | 0.0155605 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356383 | CTGAGGTCAGGCTGC[C/T]CCGGGACAGCACAGG | 10580 |
rs758654119 | snp | A/G | 0.000125117 | 0.00790841 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356627 | GATGGAGCCCAGGAA[A/G]AGGCCAGATCGGTTG | 10580 |
rs758668055 | snp | C/T | 1.8636e-05 | 0.00305249 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337222 | TGACAGCGTGCATCT[C/T]GGGGGACAGGGCTCG | 10580 |
rs758671301 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316659 | CTAAAATGATAGCCA[C/T]GTGTGACTACTGAGC | 10580 |
rs758685738 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439485 | CACTGGACGAGAAAG[C/T]AGCTTTAGGCTACAG | 10580 |
rs758691496 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457496 | ACCCACATAGCACAG[C/T]GCTTGACACACAGGA | 10580 |
rs758693737 | snp | C/T | 2.58114e-05 | 0.00359236 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422220 | CTGGCTCCAGACCTA[C/T]ACGTGGTGCAGAAAG | 10580 |
rs758716906 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398722 | TCCCTAGAACACTCA[C/T]ATACTCAAAGCCTCT | 10580 |
rs758735642 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333260 | TCTAAATAACAAGAC[C/T]CCTTTGCTAGCCAAG | 10580 |
rs758747798 | snp | A/G | 9.59739e-05 | 0.0069266 | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95416063 | CTGTCTGGGGGTGCC[A/G]AGTGGGACATAAGGC | 10580 |
rs758752580 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95509984 | CCAAACTTAAGCTAT[A/G]AAAAGTAAATAACAC | 10580 |
rs758760592 | in-del | -/AA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494090 | AAATGTAAAAAAAAA[-/AA]AAAAAAAAAAAAAAA | 10580 |
rs758762302 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515443 | CAGTCACCATTTCTC[A/G]GGGTGACTTTAATGA | 10580 |
rs758762770 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95328706 | CCCAAAGTAAAATGA[G/T]TTTCCCATCATTCTC | 10580 |
rs758781564 | snp | C/T | 1.8039e-05 | 0.00300319 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422119 | TCACAGGGAATAACT[C/T]CCTGGTTCCCCTGTA | 10580 |
rs758808685 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426560 | TAATGGAGACATGGC[-/A]AAAAGGCTGAACACA | 10580 |
rs758811470 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323922 | AGGCCACAGTGAGCA[A/T]GATTGCACCGCTGCA | 10580 |
rs758821274 | in-del | -/ACA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95432331 | CACACACACACACAC[-/ACA]CCCCCCCCCCCCAAG | 10580 |
rs758870899 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434419 | GTCCTCAGTTCCTCC[C/G]CACATTCGCTGGCTC | 10580 |
rs758878204 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487202 | AGACAGAACACTACA[C/T]AATTAATGTTCATTT | 10580 |
rs758885184 | snp | C/T | 0.000218317 | 0.0104456 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384373 | TTCCACAGTCTGGTA[C/T]GAGCATCCAGCCCCC | 10580 |
rs758897807 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458472 | TATACAAGTACTGAG[C/T]TGGCGCATAAATTGC | 10580 |
rs758899944 | snp | C/T | 1.82061e-05 | 0.00301708 | missense | SORBS1 | GRCh38.p7 | 10:95341653 | TATAAATGTAAACAA[C/T]ATCTCCCTTCTGCAG | 10580 |
rs758903568 | snp | A/G | 1.67894e-05 | 0.00289731 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384413 | CCAGCGGACAGAAGA[A/G]TGAAGCGCCAGAAGC | 10580 |
rs758904536 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95348568 | ATTCACTGATTCCAT[C/T]GAACTCTTGAGACGT | 10580 |
rs758923189 | in-del | -/AAAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498538 | AAATTTATCTGAATA[-/AAAG]AAAGAAAGAAAGGGC | 10580 |
rs758933976 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487987 | TGGCCTTCTTCAGAA[A/G]ATTTTATGATGTCTA | 10580 |
rs758940665 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527933 | TGCATCTAATTGATA[-/T]CTCCATGAAAATTAA | 10580 |
rs758941748 | in-del | -/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449384 | TGGGATTATAAGCAC[-/G]TGCCACCTTGACTAC | 10580 |
rs758947405 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466549 | AAATAAATCTAAGCC[A/C]CAACACTGAAAAACC | 10580 |
rs758957629 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488864 | ACCCTAATCTCCTGC[C/T]TGGACCACTGGAAGG | 10580 |
rs758971666 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95556077 | AGACACTTTTTCCAT[A/G]GAAGGAAGTCTAGAA | 10580 |
rs758988861 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95417851 | TCTTGAGCTCCTGAC[C/G]TTGTGATCCACCTGC | 10580 |
rs759002445 | snp | C/T | 1.71296e-05 | 0.00292652 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410825 | GTAAATATAAAAAGC[C/T]AGTGTTAATGTTTTT | 10580 |
rs759006125 | snp | A/G | 1.6996e-05 | 0.00291508 | intron-variant | SORBS1 | GRCh38.p7 | 10:95381676 | AAATAACTTTAATAT[A/G]CACATTACCATCTTT | 10580 |
rs759015654 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95527262 | AACCTCGTCCTTACT[A/G]AAAAAATACAAAAAT | 10580 |
rs759022177 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363613 | TTATAGATCTGAAAT[A/G]CTAGGAAAATAAAGT | 10580 |
rs759023048 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334105 | TTTAGTTCAGCAAGG[A/T]GAATAATGGCTGACA | 10580 |
rs759025125 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95342889 | TATTATTATTTTTTT[A/T]TTTTTTTTTGAGACG | 10580 |
rs759027684 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant | SORBS1 | GRCh38.p7 | 10:95322040 | AGAAATGATTAAAGA[C/T]GATTTATTGTCAGAA | 10580 |
rs759032105 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95376825 | TAGACAAGACAGATA[A/C]CAGAACAAAGGGGAA | 10580 |
rs759057827 | snp | A/G | 3.29674e-05 | 0.00405988 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95322778 | ATTCTGTGAGATCTG[A/G]TCCTGCTCTCAATGA | 10580 |
rs759062877 | snp | A/G | 1.7258e-05 | 0.00293747 | intron-variant | SORBS1 | GRCh38.p7 | 10:95422089 | CTGAGAAATAGAGAG[A/G]AAAAAATCTCTCACT | 10580 |
rs759110173 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549911 | TGATTTTAATACCAA[C/T]GCATTTGAGTCCCCC | 10580 |
rs759122350 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95387406 | TCTAATGGAAGGATA[C/T]TTTACCTCAGCTTAT | 10580 |
rs759137925 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335418 | ACTATTTACTGTGGA[C/T]ATCAGACATACTAGA | 10580 |
rs759143858 | snp | C/G | 1.65113e-05 | 0.00287322 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337246 | GGGCTCGGCGGGAGT[C/G]GGGCAGAGATGAGGG | 10580 |
rs759150356 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95364554 | GCTTCCCGGGGAAGC[A/G]ATCCTCCACCTCAGC | 10580 |
rs759162002 | in-del | -/GGAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333818 | GTCAGTAATTTTTAG[-/GGAA]ACTTCAAGGATAAGA | 10580 |
rs759175923 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385755 | GAACAGGGCTTAAGG[-/T]TTTTTTTCTACCAAC | 10580 |
rs759212313 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95458118 | ATGAGAAAATGCAAT[A/G]TCCAGGTACACGTCC | 10580 |
rs759229328 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488753 | TGTTTTTACTCACAT[A/G]CCACATGCAACCTAG | 10580 |
rs759236711 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320380 | TCTTCCTTCACTTAC[-/T]TTTTTTTTTTTTTTT | 10580 |
rs759245798 | snp | C/G | 4.94556e-05 | 0.00497246 | missense | SORBS1 | GRCh38.p7 | 10:95410767 | ACTTCATTTAGTAGA[C/G]GACTGGAATCCTGAA | 10580 |
rs759250258 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95449709 | TTTTTACCTTTTATA[C/G]TTGAGTGGAGCTTTT | 10580 |
rs759254512 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476281 | TTTCCAGGGCAAAAA[C/T]GTCCTACAGGGCAAA | 10580 |
rs759259398 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95437439 | TGACATACTCCGCAC[C/G]TTTAGAAATGCCTTC | 10580 |
rs759269573 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95545662 | TACTCCAGCCTGGGT[A/G]GCAGAGTGAAACTCC | 10580 |
rs759299980 | snp | C/T | 1.65312e-05 | 0.00287495 | missense | SORBS1 | GRCh38.p7 | 10:95341599 | AGATTCCCACCCGGC[C/T]GTGGTGTTCTCCTTC | 10580 |
rs759305535 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560388 | TGTCTGCCTGGAGAA[A/G]GCATGCACTGGTGAA | 10580 |
rs759307472 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95463920 | GGTCACAAATGTCCC[A/G]TTCTCCTGCCATTGT | 10580 |
rs759307626 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354378 | AGCAAGAGAGTTATA[A/G]GCAACTTCCTCAAAT | 10580 |
rs759316546 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95335667 | CTGAGTCTCAGACAG[-/A]GGGAAGCAACTCCCA | 10580 |
rs759338540 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383308 | GCAGTCCTAGCTACT[C/G]GGGAGCCTGAGGCAT | 10580 |
rs759339562 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395045 | TCAGGGAATTTGTAC[A/G]TAGGGAAATAAGGGT | 10580 |
rs759341689 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407876 | ACCTGAGCCTGGGAG[A/G]TTGAGGATGAAGTGA | 10580 |
rs759363654 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95494430 | TGCCAAGCCTGGCTG[A/G]GCACCTCTCTTTCCA | 10580 |
rs759366734 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95436400 | GCGACCAGGCAGGGA[C/G]GCAAGAACAGGAGCA | 10580 |
rs759368273 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95517894 | ACCCAAAGGCATCCT[C/G]TTCCAATGGGTGCAC | 10580 |
rs759368298 | snp | G/T | 1.90315e-05 | 0.0030847 | intron-variant | SORBS1 | GRCh38.p7 | 10:95414436 | GTGAGAAAGGGAATG[G/T]GACTGCTGGGAGGAG | 10580 |
rs759375583 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464925 | CAGGTGGAAAAGGAA[A/C]AAGTCTACCCACAAA | 10580 |
rs759377927 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95466141 | AACAGTGCAAGACTC[-/A]GAAAAAAAAAAAAAT | 10580 |
rs759388134 | snp | A/G | 8.2848e-05 | 0.00643561 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371976 | CGGAGGAGGCACAGC[A/G]GAATTACCTTTCTAT | 10580 |
rs759406292 | snp | A/G | 3.37058e-05 | 0.00410509 | intron-variant | SORBS1 | GRCh38.p7 | 10:95371455 | AGAAAAGATGGGAAA[A/G]AAGGTTTTAGTTTAG | 10580 |
rs759419539 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95425575 | ATGAGCATTGTTGAT[C/T]TCTGCCATGTGATAA | 10580 |
rs759441048 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95384200 | CATCCACCACTTTCC[C/T]TTCCGCCCCCACAAC | 10580 |
rs759441424 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | SORBS1 | GRCh38.p7 | 10:95437546 | ACAGCTTTGGAACCA[C/T]CATCACATTCTGCAA | 10580 |
rs759447252 | in-del | -/TTTTTTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548449 | AGTTCTTTTCTTTCC[-/TTTTTTT]TTTTTTTTTTTTTTT | 10580 |
rs759459291 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413101 | AGTTTTGCAGGCATA[C/T]ATCTTTACACAAAGG | 10580 |
rs759487479 | snp | C/T | 5.06675e-05 | 0.00503301 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414841 | TTACCTCCGGCTGGG[C/T]TGCACTGGAGGAAGT | 10580 |
rs759492978 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant | SORBS1 | GRCh38.p7 | 10:95315142 | CTATGAAAAAACACA[C/T]ACATACAAAACATGA | 10580 |
rs759497652 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95371723 | AATGCCTATTTTCTC[-/T]TTTTTTCAGAGTGTG | 10580 |
rs759512927 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95454652 | AAACAAAGACAAACG[G/T]ATCCTCTTTGGGTGC | 10580 |
rs759523494 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540125 | GCACATTCTCTTCTC[C/T]TTTGTGGGCCTCAGT | 10580 |
rs759530457 | in-del | -/A | 1.65785e-05 | 0.00287906 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434592 | GATCCGCTCACAGTT[-/A]AGAGAAAATCGACCG | 10580 |
rs759531366 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95516889 | TTTCAAGTTGGAGGG[C/T]TGGAACTCAGGTTGC | 10580 |
rs759555709 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95542579 | GTAATTACTTCAAGC[C/T]CTGGGACTTGAAAAC | 10580 |
rs759558576 | snp | G/T | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95313689 | CCCTCACACCCTTCT[G/T]AGCACATATCACAGT | 10580 |
rs759582902 | snp | C/T | 6.61146e-05 | 0.00574917 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95336918 | CCTGAAGATGGCGTG[C/T]GGACACCACCGTCTC | 10580 |
rs759591703 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473488 | CAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCACC | 10580 |
rs759611907 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426645 | ACTGCTGGGAAATAA[G/T]ATGTCCTGACTCTCC | 10580 |
rs759661799 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474665 | TCCACAGCTCAAAAA[C/T]AGGACTTAAGTACTA | 10580 |
rs759673911 | snp | A/C | | | upstream-variant-2KB, intron-variant | SORBS1 | GRCh38.p7 | 10:95442665 | ACTGTGAGCCAATTA[A/C]ACCCCTTTTCTTTAT | 10580 |
rs759677200 | in-del | -/AAT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95426640 | ACATCACTGCTGGGA[-/AAT]AATATGTCCTGACTC | 10580 |
rs759679353 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513783 | ACCATCTAGAAAGGA[C/T]TCTTTTAAGTCTAAC | 10580 |
rs759688277 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492390 | AATATTTATTGAGCC[C/T]TATTACACTCCAGGA | 10580 |
rs759688938 | snp | A/G | 0.000529898 | 0.0162686 | missense | SORBS1 | GRCh38.p7 | 10:95339269 | TGTCGGGATGTCCCC[A/G]GGATCCTCCCTTCGT | 10580 |
rs759692153 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467769 | GGGAAAGAAACCTCC[-/A]CAGAAACATGACTTC | 10580 |
rs759705911 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95404656 | GCCCCGTGCAGTGCA[A/G]GGTACAAAGGAAGCC | 10580 |
rs759721189 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95462440 | TCTATAATGTCACCA[C/G]CCTAACACAATCTCA | 10580 |
rs759728735 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393171 | TAGACTCTTCTTGGC[C/T]TTGAGGAAGACACTG | 10580 |
rs759733517 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514750 | AGACCCATCATCATT[C/G]ATAGAGAAGTTGTGA | 10580 |
rs759735085 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476176 | CTCAAACAGCAGGTG[-/C]CCAGTGATAGCTGAT | 10580 |
rs759750421 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367943 | CTCCTGGTCTTTTGC[C/T]TTCCAGTGGATGCAG | 10580 |
rs759776788 | snp | A/G | 0.000135621 | 0.00823359 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355740 | TAGTCCTCCAGGGCC[A/G]TGGGTCTCTCCTGAG | 10580 |
rs759778767 | snp | C/T | 1.6596e-05 | 0.00288058 | missense | SORBS1 | GRCh38.p7 | 10:95339186 | AGAAAGGCAGGTCCA[C/T]GTAATCCACAGGGTT | 10580 |
rs759800979 | snp | A/C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95502852 | GCTCCTCTGGAAACT[A/C/T]CCTTTTACTTTTCAT | 10580 |
rs759802978 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95525825 | AAAGTGGAATTATAG[A/G]ATAAAGTGGGTATCT | 10580 |
rs759821311 | snp | A/G | 3.29783e-05 | 0.00406055 | synonymous-codon | SORBS1 | GRCh38.p7 | 10:95384014 | CTTCAGTGAGGAAGA[A/G]CGGGCTGGGAGGGGT | 10580 |
rs759822763 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95382247 | CTAACTAGGTGATCT[C/T]AGACAAGTATTTCAC | 10580 |
rs759841960 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411138 | CAAATGCGATCCAAG[A/G]ACAAGAGCTGGTTTA | 10580 |
rs759844359 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369008 | TGCTGTACCTCTGCA[A/G]GCTCCAGATTCTTTG | 10580 |
rs759851859 | in-del | -/CTCA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445212 | GTTCTGTTGTGTGTT[-/CTCA]CTCTGGTGATTAAAT | 10580 |
rs759853146 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381127 | TAATTGCTTAGAGAT[A/G]TAAACTTGTATAGGG | 10580 |
rs759868865 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95424066 | GCATCAGGGCTTGCT[C/G]AAACACAGGTGGCTG | 10580 |
rs759869788 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95352230 | ATTTTTAAAGGCTTC[C/T]TTGAAAAATCAAACA | 10580 |
rs759870809 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507748 | AACCCCATCTCTACT[-/A]AAAATACAAAAATTA | 10580 |
rs759882117 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95450877 | AAATTCTAATAGTGA[G/T]TGTGGTAGCATAGAA | 10580 |
rs759886917 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95327423 | GTGGGTGACCCTGCA[C/T]GCGTCCTTGCTGTTG | 10580 |
rs759896588 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95524296 | AGATCAGGTGAGATG[C/T]CAAAGATATCATGCA | 10580 |
rs759906940 | in-del | -/CATGCGCGCGCGCG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358703 | ACGCACATGCACAGA[-/CATGCGCGCGCGCG]CGCGCGCACACACAC | 10580 |
rs759927026 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95451408 | CTGAACTCCTTCTCA[A/T]ATCCTTTATATGTAA | 10580 |
rs759942055 | snp | C/G/T | 6.61872e-05 | 0.00575238 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394967 | AATTAATTTAAAGCT[C/G/T]GGACAACAGATATGC | 10580 |
rs759956622 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480550 | CCTAGGACAAGCTGT[A/G]TGACTTCAGGCCAGG | 10580 |
rs759958045 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95401305 | TGAGCCTGGGAGTTC[A/G]AAGCTACAGTAAGCC | 10580 |
rs759968457 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95377447 | TAAAAGAATCTTTAG[C/T]ATTACTTTCACTTTT | 10580 |
rs759982001 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95440055 | CTTGGGTGACAGATC[A/G]AGACTCTGTCTCAAA | 10580 |
rs759997871 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95521093 | TGCCCTGAATTCAAA[A/G]TAATTACCACAGATG | 10580 |
rs760010781 | snp | A/C | | | upstream-variant-2KB | SORBS1 | GRCh38.p7 | 10:95562539 | CAGCTTCCCACATCC[A/C]TGAAGATAAGACACT | 10580 |
rs760017085 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | SORBS1 | GRCh38.p7 | 10:95357705 | TCACCACCTTCCAAG[A/G]CACTTTTATAAATTT | 10580 |
rs760017916 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490101 | GTCATACCTGGAGGC[A/T]CTCTCACCTCAGCAC | 10580 |
rs760018067 | snp | A/G | 1.73954e-05 | 0.00294913 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414609 | GTCTGGCTAATGGGG[A/G]CAAAGGAGCCAGAGG | 10580 |
rs760019059 | snp | A/G | 6.59391e-05 | 0.00574153 | missense | SORBS1 | GRCh38.p7 | 10:95384091 | TCTCACTTTTTGAGC[A/G]AGGCACAGAAAGGGG | 10580 |
rs760024363 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358318 | ATATAAAATCATCAA[C/T]GAAAGGGGGAAGCCC | 10580 |
rs760031589 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95512862 | TCTCTAAAAGAAACT[C/G]AGGCAAATAGCTCCT | 10580 |
rs760062995 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469876 | CTTGTCAAAGGGCAG[A/T]CTGCTGAGCTCTGGC | 10580 |
rs760063927 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549698 | GAAGTTATGAAAAAA[C/T]ACTTAAATGTTTTTA | 10580 |
rs760066482 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95385939 | AACAGAACGTCTGAT[C/T]ATACTGACAAAATGC | 10580 |
rs760085642 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528803 | ACATGCCTGTAATCC[-/C]AGCTATTCAGGAGGC | 10580 |
rs760103769 | snp | C/T | 3.66683e-05 | 0.00428168 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95414545 | GACTCTGCGGAGGTC[C/T]TCCGGGGCAGGAGGG | 10580 |
rs760105262 | in-del | -/TTT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95507983 | AGTAGTGGCCCAGAC[-/TTT]TTTTTTTTTTTTTTT | 10580 |
rs760106134 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487247 | GTTCCAGAAGTACCA[C/T]TCAGAGTGTTTTCAC | 10580 |
rs760121097 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498592 | AAATTGGAGGTCAAC[A/G]GGCCACACCAGGCCT | 10580 |
rs760136160 | in-del | -/AAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362932 | TTTAGTTATTTCAAG[-/AAG]AAGAAGAAGAAAAAA | 10580 |
rs760141054 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95407947 | TGAGACCTTGTCTCA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 10580 |
rs760141768 | snp | A/G | 1.72642e-05 | 0.00293799 | missense | SORBS1 | GRCh38.p7 | 10:95357801 | AAGTTGGAAGAATAT[A/G]TACTATGAACAGGTA | 10580 |
rs760143998 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95459706 | CAGCTCTGCAACCTC[A/C]TTAAGTTCAGAGTGA | 10580 |
rs760151363 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399932 | GCAGACATTGTGCTC[G/T]GCCTTGTGGACATGA | 10580 |
rs760171745 | snp | C/G | 1.69965e-05 | 0.00291513 | intron-variant | SORBS1 | GRCh38.p7 | 10:95432421 | TTCCCACGTGGCTTT[C/G]AACAGCTTTCCCTAG | 10580 |
rs760196664 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95346290 | TGAACTACTGTTTTG[A/T]TCTTTTTTTTTTAAC | 10580 |
rs760202775 | snp | G/T | 1.67016e-05 | 0.00288973 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410799 | CGAACAAACAAACAA[G/T]GTAACTAACTGTAAA | 10580 |
rs760207970 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434528 | TAAACATGCAACGAT[C/T]CAGCTCAAAGTGCGT | 10580 |
rs760208240 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95536968 | CCACCATCTGGGTCC[A/G]ACTTACTTCACAGTC | 10580 |
rs760223321 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95399831 | ACTGGAAGATATAGA[C/G]CACTAACAAAGATAC | 10580 |
rs760232038 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95457094 | TAAATAAAGACACTA[C/T]GATATCAACCACTAC | 10580 |
rs760256189 | in-del | -/GTAGT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95337794 | CAGAGAGGAGTATGA[-/GTAGT]GTAGTGTACTAGTTT | 10580 |
rs760257090 | snp | C/G | 4.95446e-05 | 0.00497693 | missense | SORBS1 | GRCh38.p7 | 10:95346428 | TCTGAGCTTTAAAGT[C/G]AAATTTGGCTCTGGC | 10580 |
rs760263934 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515409 | CCTTGGGTCCCTCAG[G/T]ACTTAATATGGCCAC | 10580 |
rs760266883 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95347646 | TCACCATGTTGGCCA[C/G]GCTGGTCTCTAACTC | 10580 |
rs760268586 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95369622 | TAATCCCATCCCCCA[A/G]TTCTTTGCTCTTTAC | 10580 |
rs760283165 | in-del | -/AAAAAAAAAAAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95528934 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]AAAACTGTTTCCACA | 10580 |
rs760310626 | snp | A/C/G | 0.000282118 | 0.011874 | missense, synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336929 | CGTGTGGACACCACC[A/C/G]TCTCCATTCATGTGA | 10580 |
rs760312386 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95363185 | CACTGGACTCTGGTT[A/G]TTTACAAATCTGTCT | 10580 |
rs760323979 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95488545 | TCATGGCTTTAAATA[C/T]CATCTACATGCCAAT | 10580 |
rs760327777 | snp | C/T | 1.91389e-05 | 0.0030934 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336521 | ATGCTGCAGTCCTAC[C/T]TGGCTCCCACCTCTC | 10580 |
rs760330761 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95317309 | GATTTCAGGAGAGAT[A/G]GGTGGCCTGAGTTCA | 10580 |
rs760342530 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480118 | GGAGACAGGGGAGGC[A/G]GTGATGGCAGCCAGG | 10580 |
rs760344757 | snp | C/T | 1.656e-05 | 0.00287745 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95372042 | TAATCCCATATCTTT[C/T]TGGGAGGCTGACGGG | 10580 |
rs760345134 | snp | G/T | 1.66724e-05 | 0.0028872 | missense | SORBS1 | GRCh38.p7 | 10:95341623 | CTCCTTCATACCAGT[G/T]CTGATCAATTTGCTT | 10580 |
rs760347089 | snp | A/G | 1.65293e-05 | 0.00287479 | missense | SORBS1 | GRCh38.p7 | 10:95357646 | CTTTAGTGGAAGCAG[A/G]GCTGGATGGTCGCTT | 10580 |
rs760355013 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | SORBS1 | GRCh38.p7 | 10:95318349 | TCGTCACATTTTTCC[A/G]TGACATCAACGATAT | 10580 |
rs760356623 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95406951 | ATCTCCTTTGTGGAG[A/T]CCTAATGTGTACGTG | 10580 |
rs760361946 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95469721 | AGGGGAGAGAAGACA[A/G]ACAAATTCACTTTCC | 10580 |
rs760368618 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95333847 | TAAGAGGGAAACTTT[C/T]CCTTGGCCCCAACAG | 10580 |
rs760374897 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95498487 | TAAAAAAACTGTCTA[A/C]TTAAATGGTTAAAAC | 10580 |
rs760380824 | snp | A/C | 3.30387e-05 | 0.00406427 | intron-variant | SORBS1 | GRCh38.p7 | 10:95394605 | ACACAATTTTCCTTT[A/C]ATTACCTTCAGATTT | 10580 |
rs760401000 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95487723 | TGAGACGATTTGTCT[A/G]GGAAACAGACAAAGC | 10580 |
rs760408116 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419748 | GAACTACTTTTTGTT[A/G]TAAACATTGTAGGAA | 10580 |
rs760453773 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474893 | CTCAAGAGCAATAAA[A/G]AGTTTCTATTGCAAA | 10580 |
rs760479272 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95504673 | TCACAGGGTTGTGAT[A/G]AGCATCAAGAGTAAT | 10580 |
rs760486402 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95393603 | AAGGTTTTCTGTGGC[A/G]TTCTGGACACACGCT | 10580 |
rs760493705 | snp | C/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95312431 | GGGGCTTGCCTTTAC[C/G]CGGAAGCATGGCTAA | 10580 |
rs760498311 | snp | C/T | 1.69215e-05 | 0.00290869 | intron-variant | SORBS1 | GRCh38.p7 | 10:95434748 | GGTAAATGGTGCATC[C/T]AGAAAGAACATTTGG | 10580 |
rs760499380 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446154 | GCGGGGAGTCAAACC[A/G]CCATTCCACGCTTTG | 10580 |
rs760500975 | in-del | -/AGAGAGAA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95357362 | ATTAGAATGAGAGAG[-/AGAGAGAA]AGAGAGAAAGAGAGA | 10580 |
rs760519915 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555731 | ATCCATCAAAGAATC[C/T]GGGAACTTTACACCA | 10580 |
rs760552290 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95435228 | TCTTGTGCCTGCTCC[A/G]ATAATTGTAGCCCTC | 10580 |
rs760554529 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95447577 | CCCCAGAATAAATGC[C/T]TGGCCTTATTTCTTT | 10580 |
rs760572504 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95323404 | TGAGATGAATTCAGA[C/T]AGCTTGTAGGACAGA | 10580 |
rs760576613 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95315155 | CACACATACAAAACA[C/T]GAGAAGACCCACTCG | 10580 |
rs760582296 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95354037 | CCAGGTCAAGGTGAT[G/T]TTTCCAGCTCTTAAT | 10580 |
rs760601712 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95386955 | ATCTCTACAAAAAAA[-/T]TTTTTAAAAAATTAG | 10580 |
rs760620721 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | SORBS1 | GRCh38.p7 | 10:95406086 | TTCAACAGGAACAGG[A/G]ATTAACACATAAATA | 10580 |
rs760627762 | snp | C/T | 1.65037e-05 | 0.00287256 | missense | SORBS1 | GRCh38.p7 | 10:95399175 | GCTCTCCCACTCTTC[C/T]TTCTGAGACAGGATC | 10580 |
rs760636312 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95544651 | CTGCACCCTACTGTC[A/T]AGGGCATCTTACAAC | 10580 |
rs760659916 | snp | A/G | 1.64953e-05 | 0.00287182 | missense | SORBS1 | GRCh38.p7 | 10:95441134 | GACTTACCAGAACTC[A/G]TGGTGGTGGCAGGAC | 10580 |
rs760660005 | snp | A/G | 0.000185718 | 0.00963455 | intron-variant, missense | SORBS1 | GRCh38.p7 | 10:95415671 | GGAGGAGGAGCAGGG[A/G]GTGGTTTTCCTGTGC | 10580 |
rs760660287 | snp | C/T | 0.000136528 | 0.00826108 | intron-variant | SORBS1 | GRCh38.p7 | 10:95355784 | GCGGCTAAGCCTGGC[C/T]ATGGTGTGTCGGGAA | 10580 |
rs760666491 | in-del | -/AATG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95481774 | TGTGTTGGTTGAATA[-/AATG]AATAAACAAATCAAT | 10580 |
rs760673170 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554051 | CTAGTAGTATTGACT[-/T]TTTTTTTTTTTTTTT | 10580 |
rs760689712 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95324316 | GGGGTTTCATGCATT[A/C]CTCAACATCACACAG | 10580 |
rs760690866 | in-del | -/A | 7.64321e-05 | 0.00618144 | intron-variant | SORBS1 | GRCh38.p7 | 10:95357835 | TTGAAAGAAAGAGAG[-/A]AAAGGGAAAAAATAA | 10580 |
rs760692061 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95398705 | GACTGCCCATAACAT[C/T]GTCCCTAGAACACTC | 10580 |
rs760699945 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95375973 | AGCTATTAAACTTAC[C/T]GGTTTCCCAAACTCC | 10580 |
rs760736668 | in-del | -/AC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95506264 | TGTGCACACACATAC[-/AC]ACACACACACACACA | 10580 |
rs760751618 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95443416 | AGCCAAGTTCGTGTG[C/T]GCCACTGCACTCCAG | 10580 |
rs760754557 | in-del | -/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95430640 | TGTAAGGTTATTTGA[-/C]TGGGCCAGGGGACTG | 10580 |
rs760756228 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95513400 | AGTTGGCCAAACACA[C/T]GTGAGGGAGGTGCAG | 10580 |
rs760776784 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522608 | CTTAGGGGACACACA[A/G]GAGCCGATTTCCAAG | 10580 |
rs760777761 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95403510 | ATAGCATCAGTCTTA[C/T]TTTAGAGCCAAGGAA | 10580 |
rs760796798 | snp | A/C | 3.37274e-05 | 0.0041064 | missense | SORBS1 | GRCh38.p7 | 10:95339292 | CCCTTCGTACCAGTT[A/C]TCATCTACCTGCCGG | 10580 |
rs760813297 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95331270 | CCATCCTGATTTCCC[C/T]GAAGACCCCTGCATT | 10580 |
rs760814336 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95413820 | GCCCTTTGACTTCCT[C/G]TGACCACTGGGGCAC | 10580 |
rs760814667 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95431346 | GAACCCTACATTCTA[A/C]AACTCCAGGCTGGGG | 10580 |
rs760818274 | in-del | -/GG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476576 | ACCTAATGTCTTAGT[-/GG]GGATTCAATGGATGG | 10580 |
rs760820355 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95523843 | TGATTATTTCTCATG[C/T]ATTTGGCAAAAGCAA | 10580 |
rs760824024 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95501897 | ATTGCTCTGCCCTTC[C/T]AGGAGCCGACAGGAA | 10580 |
rs760825315 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95540443 | AAGTGGTTCACCCCT[C/G]TAATCCTACTGCCTT | 10580 |
rs760829147 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95429161 | CCTATACTCACATCC[-/T]CATTTTTTTTTTCTT | 10580 |
rs760842078 | snp | A/G | 1.691e-05 | 0.0029077 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341246 | ATAGCTGCGCCATCC[A/G]AGAGAGCCCCAAAGC | 10580 |
rs760860973 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560894 | TTTACAGCACAAACC[C/G]ATTCGGGCTTTGATG | 10580 |
rs760870231 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95375578 | AAGCAGAGACAATGC[C/T]GGTCTTCTCAGTGTG | 10580 |
rs760892822 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95489779 | CAGGGGAGTCTAGAC[A/G]GCCAGCCTCCTGTGG | 10580 |
rs760900119 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95338759 | TGTCGTCCAGGCTGG[A/G]GTGCAGTGGCATGAT | 10580 |
rs760919232 | snp | A/G | 1.65578e-05 | 0.00287726 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336614 | TCCTGGAAAAGCGCT[A/G]CCCAGGGGCTTGCCG | 10580 |
rs760937216 | snp | C/T | 3.29843e-05 | 0.00406092 | missense | SORBS1 | GRCh38.p7 | 10:95384273 | CTGGGAGAGTACAGA[C/T]CTGAATCATCATCTA | 10580 |
rs760946216 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95390256 | TCTGGGGCTTCACCT[A/G]GACTCGCCTTCTCAC | 10580 |
rs760952536 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95391444 | CTGAGATGTTGGCCA[C/T]CACACTGCTGTTCCT | 10580 |
rs760955195 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95351104 | GCCAGGATGACAGAT[A/G]CTGTTTGGAGAACTA | 10580 |
rs760959578 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464071 | GTGGATCACGCCTGT[A/G]ATCCCAGCACTTTGG | 10580 |
rs760968160 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95320670 | GGTGTGAGCCACCGC[A/T]CCTGGCCTCACTTAC | 10580 |
rs760991550 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95383252 | AACCCTGTCTCTACT[-/A]AAAAAAATACAAAAA | 10580 |
rs761006823 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95316571 | GGTGCTCCTTCCCAC[A/C]CCTAAGTTCTCATAA | 10580 |
rs761008473 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95338855 | CTGGGACTACAGGCG[C/T]CCGCCACCACGCCTG | 10580 |
rs761008761 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95460502 | GAACCACTTGAGCTC[A/G]GGAGTTTGCGACCAG | 10580 |
rs761008780 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95361118 | CATGCCCAGCCTGTC[C/T]AGAACTTCTAAGCCA | 10580 |
rs761020678 | snp | C/T | 5.40438e-05 | 0.00519798 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337201 | TCAGTGAGATCCACT[C/T]AGAGGTGACAGCGTG | 10580 |
rs761054616 | snp | A/C | 1.70711e-05 | 0.00292152 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414625 | CAAAGGAGCCAGAGG[A/C]GCGGGCTGGCTGGCT | 10580 |
rs761057004 | in-del | -/AGA | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445065 | GGATGCTGAGAGGGT[-/AGA]AGAAGGAGAATGGAC | 10580 |
rs761061852 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95461620 | TATTAAACGCTGATG[C/T]TCAACCCCAAACTGT | 10580 |
rs761084697 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95473228 | ATTGTTTATGTATTA[C/T]GGCACTTCTACTCAA | 10580 |
rs761096290 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95520948 | ATTTGCTAAAATGGA[C/T]ATTTCTACAAAAAGA | 10580 |
rs761097274 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95490881 | GTAAAAATGGCAGAA[C/T]CAAGTAAGTACCAAA | 10580 |
rs761125993 | snp | A/G | | | utr-variant-3-prime | SORBS1 | GRCh38.p7 | 10:95315013 | ATCGGTTCATGAATG[A/G]TGCTTCCTCCTCCAA | 10580 |
rs761134525 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95549608 | AAAATATCTTCCACT[A/G]AGCTAAATCAATATC | 10580 |
rs761136098 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95492093 | AATTATCAAAAATAA[C/T]ACTTTCAGAGAAGTA | 10580 |
rs761156808 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95325107 | CTGTAGGCGGCAAGG[A/G]TGCAGAGGACCTCAA | 10580 |
rs761158547 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95368911 | GTCCAGTCTTCCACC[C/T]TGAAAAAACTTTGAC | 10580 |
rs761162063 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351294 | AACTGATGGTGCGTC[A/G]GAATGACGCCTGTGT | 10580 |
rs761164120 | snp | A/T | 2.27038e-05 | 0.00336918 | intron-variant | SORBS1 | GRCh38.p7 | 10:95367714 | TCTGTACATGTCCAA[A/T]AAAGAAAAAAAAGAA | 10580 |
rs761171964 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535497 | CATTTGTACTGATAA[C/G]AGTTTTCTAGGATCC | 10580 |
rs761174432 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95381860 | ATTAGCTTCCGACAC[A/G]GTCTGACTTTGGATG | 10580 |
rs761176795 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95395048 | GGGAATTTGTACGTA[A/G]GGAAATAAGGGTTTT | 10580 |
rs761189461 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480380 | GAAAAGTTAGATAAC[A/G]GTACGAATAGTGATA | 10580 |
rs761206352 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95559446 | AAAAGGCCAACAAGG[C/T]GGGTATCGTCCACAA | 10580 |
rs761228436 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95356509 | CGGTGTGCTTGGGGA[A/T]GTGTTCCGAGCCCTC | 10580 |
rs761261652 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95555848 | CATCTCATTCTTTTC[C/T]AAAAGGGTCTGGGTC | 10580 |
rs761269534 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95340236 | TTCTGAATAAGCATG[A/G]TGGTGATAATAATAA | 10580 |
rs761287659 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95367817 | TCTTTTTCCTAGTTT[A/T]GACCAGGACCTCTGG | 10580 |
rs761293954 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95439141 | TGTAGCTGCTTTTCT[C/T]CTAATGACCATTTTA | 10580 |
rs761302518 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405185 | TAGCTGGTGCCTATA[A/G]TCCCAGAACTTTAGG | 10580 |
rs761329839 | snp | C/T | 3.2981e-05 | 0.00406071 | intron-variant | SORBS1 | GRCh38.p7 | 10:95397287 | TCTCTCAGTGTTCTG[C/T]AGAAAAACAAAGGCA | 10580 |
rs761331772 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95411034 | AACATCATTCATTAG[C/G]TCCACCTGTTAACAG | 10580 |
rs761335103 | snp | A/G | 1.83464e-05 | 0.00302868 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95414538 | GCTCCGAGACTCTGC[A/G]GAGGTCCTCCGGGGC | 10580 |
rs761342321 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95547106 | ATGCTGAGAATCAGG[C/T]TTGCTAGGAACAGTC | 10580 |
rs761352442 | snp | G/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95355497 | GAGCCATGATTAATT[G/T]CCAAGCAAAACAAAC | 10580 |
rs761357000 | snp | C/T | 1.65496e-05 | 0.00287655 | intron-variant | SORBS1 | GRCh38.p7 | 10:95346489 | AAGTTAAAATCAGGA[C/T]TCATGGACAACAAGG | 10580 |
rs761385315 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95434299 | CTGGGGGCTGGAAAC[C/T]TCTAGGGAGAGCCTA | 10580 |
rs761393604 | snp | A/G | 5.38266e-05 | 0.00518752 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95337097 | CCTTGGTGACAAGGC[A/G]AGGTGGTCAGTGTTA | 10580 |
rs761393766 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95548164 | GACCAGTGACCAGTT[A/G]TGACACTCAGAGGAC | 10580 |
rs761398422 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95365771 | CTTCTCCAAGGTGGG[A/C]ACTGTCCCCTAAGGC | 10580 |
rs761399480 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95535858 | ATTTCCAAACCATGT[C/G]TATGTATCAAACTAT | 10580 |
rs761412701 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95560274 | ATCCAAAGGCTCGCC[C/T]AGAACATGCTGGGAA | 10580 |
rs761420534 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95533787 | CAGCAAACAGGCTCA[C/T]GGCCACATGACTGGC | 10580 |
rs761420646 | in-del | -/TAG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95522014 | ACTGAATCTGGAACT[-/TAG]TAGAATCTCAGAGTG | 10580 |
rs761464259 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95499950 | TTCCTGAGAACACAG[A/G]ATCCCGCTCTCAGCC | 10580 |
rs761469773 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | SORBS1 | GRCh38.p7 | 10:95318362 | CCATGACATCAACGA[C/T]ATCTCCATCGCGGAG | 10580 |
rs761483621 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95351264 | AGGAGGTCCCCAAAG[C/T]GCTCATTAGTGATAA | 10580 |
rs761483637 | snp | C/T | 5.38982e-05 | 0.00519097 | missense, intron-variant | SORBS1 | GRCh38.p7 | 10:95337032 | GATCGTGGGGTGGGA[C/T]GATCTGACCAACTCA | 10580 |
rs761511380 | in-del | -/GC | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95358705 | CACATGCACAGACAT[-/GC]GCGCGCGCGCGCGCG | 10580 |
rs761511593 | in-del | -/A | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95464333 | TAAAAAAAAAAAAAG[-/A]AAAAAAAAAAAGGCT | 10580 |
rs761514392 | snp | A/C | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95427791 | CAACATTCTTTCCAG[A/C]ACTCTTCACAAATCC | 10580 |
rs761514663 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95480314 | ACCTGGCTCCATGCA[C/T]GCAGAGGAAAAGCTC | 10580 |
rs761515380 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95445327 | AAGGAACTGCAGCAA[C/T]GGCAGCAGTGCCAAG | 10580 |
rs761539546 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95416527 | GACTCAAGAAGGGAG[C/T]CAAGTGAACTAAACA | 10580 |
rs761544871 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95374842 | CAGCTCAGCTGCTAT[C/T]GGGAGACAGTGTCTA | 10580 |
rs761563179 | in-del | -/AT | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95467486 | GCTGCCTGAGGAAAC[-/AT]GTGAAATATTTCCGT | 10580 |
rs761573845 | snp | A/C | 1.64931e-05 | 0.00287163 | intron-variant | SORBS1 | GRCh38.p7 | 10:95437604 | GTAAGCTGCCCCAGC[A/C]CTTACTGAGTCCTGT | 10580 |
rs761576656 | snp | C/T | 1.7318e-05 | 0.00294256 | intron-variant | SORBS1 | GRCh38.p7 | 10:95318472 | AAGTGACTCAAATGT[C/T]GACAGGATTAAATAA | 10580 |
rs761594056 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95537078 | CTGTCCATTTGCTCA[C/T]GGCAGTCCCTCCTCC | 10580 |
rs761599697 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95468144 | TCAACTGATCCACCC[A/G]CCTCGGCCTCATAAA | 10580 |
rs761617552 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95514818 | TTCAGATTCATACTG[A/G]GCCTTGAGGCAGAAG | 10580 |
rs761618299 | in-del | -/GG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95409346 | AGCCACTGCCAGTAA[-/GG]GGGGCATGGCACCGC | 10580 |
rs761622271 | snp | C/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95515281 | CTTGGTGGAGGGTGG[C/G]TGTGGATGTCAATTC | 10580 |
rs761641499 | snp | C/T | | | intron-variant, synonymous-codon | SORBS1 | GRCh38.p7 | 10:95415511 | GTAAGATTCTTTGCT[C/T]TTCCGGTTTTCGGGA | 10580 |
rs761665283 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95486443 | CATATTTGTCTAAAG[C/T]TGCTGAAAAAAGAAA | 10580 |
rs761676599 | snp | A/G | 0.000102796 | 0.0071685 | missense | SORBS1 | GRCh38.p7 | 10:95339314 | ACCTGCCGGAGCAGT[A/G]TGATCCTCTCACCCT | 10580 |
rs761711415 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95433791 | TTGAACGCAATGCAC[A/G]AAACGCACAATGTGT | 10580 |
rs761712722 | snp | C/T | 3.29576e-05 | 0.00405928 | intron-variant | SORBS1 | GRCh38.p7 | 10:95410623 | GGAGTGGGGCACAAG[C/T]CTCTCTTACCTCGAT | 10580 |
rs761714391 | snp | A/C | 1.65649e-05 | 0.00287788 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384155 | GACTTAAAACTCATG[A/C]AAACTGAGAACAGGG | 10580 |
rs761721506 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95405747 | CCTGACTCCTCACAT[C/T]CAGAAGGGAGACAGA | 10580 |
rs761733277 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95332795 | CACTGAAGTGCCTTC[C/T]ATACATTAGGTATCA | 10580 |
rs761740983 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95476764 | AAAGCTTTCCTAAAT[C/T]GACATCCCTCACAGT | 10580 |
rs761741365 | snp | A/C | 1.68332e-05 | 0.00290109 | intron-variant | SORBS1 | GRCh38.p7 | 10:95341262 | AGAGAGCCCCAAAGC[A/C]AGGCATGAGAAGTGC | 10580 |
rs761766769 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant | SORBS1 | GRCh38.p7 | 10:95336788 | CCTCTCATATTGTCC[A/G]CTCTCTTCGCGCCAT | 10580 |
rs761772300 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95526908 | AGGTTTTCTGACATA[A/T]AGTTCAATCTTCTTT | 10580 |
rs761774003 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95474763 | AAGTGCCCATGTTTG[C/T]GAACAAACATGAGAA | 10580 |
rs761782166 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95362985 | TGGCTTTGCAGGAAG[A/G]AGTCTAGATAATCCT | 10580 |
rs761802255 | snp | C/T | 4.95667e-05 | 0.00497804 | missense | SORBS1 | GRCh38.p7 | 10:95406135 | GAAAGGCTACTGAGT[C/T]GTTTTTGCTGTTCTG | 10580 |
rs761805409 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95334531 | CCACCAAGAAAGGAA[C/T]ACCAAGTTTCAACAA | 10580 |
rs761823307 | snp | A/G | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95322169 | CTGTGAGGTGGCCCC[A/G]AGATATCCAGAAACC | 10580 |
rs761824662 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95452409 | TAATAAATGCAAGAC[C/T]TTGGCTCCCATCACT | 10580 |
rs761836582 | in-del | -/TAGGGAGG | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95419425 | TGCTGATAATGGCAG[-/TAGGGAGG]TAAGCAAAAGATCAT | 10580 |
rs761837143 | snp | C/G | 4.95242e-05 | 0.0049759 | intron-variant | SORBS1 | GRCh38.p7 | 10:95384294 | TCATCATCTATTGAA[C/G]AAAACAAAATGTAGT | 10580 |
rs761846177 | snp | C/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95534689 | TAAGTATTTGAGTGA[C/T]TATTAAATGAAGAAG | 10580 |
rs761861007 | snp | A/G | 0.000120926 | 0.00777486 | intron-variant | SORBS1 | GRCh38.p7 | 10:95356144 | GAAATCTCCATGAAC[A/G]CTGCCGCCACTGCCT | 10580 |
rs761862347 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95554045 | ATTTTTCTAGTAGTA[A/T]TGACTTTTTTTTTTT | 10580 |
rs761866545 | snp | A/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95446041 | CAAAAGGACCAACAG[A/T]GTACCATCTAGTGGC | 10580 |
rs761873123 | in-del | -/T | | | intron-variant | SORBS1 | GRCh38.p7 | 10:95349442 | CTTCCCCAGCTTTCC[-/T]TTTTCTTTTAATTTG | 10580 |