Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1126772 | 0.851 | 0.320 | 4 | 87983034 | 3 prime UTR variant | A/G | snv | 0.16 | 5 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs11574944 | 1.000 | 0.200 | 16 | 30498669 | intron variant | C/T | snv | 0.25 | 1 | ||
rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
rs11642873 | 0.851 | 0.280 | 16 | 85958099 | intergenic variant | A/C | snv | 0.15 | 4 | ||
rs116799036 | 1.000 | 0.200 | 6 | 31381371 | downstream gene variant | G/A | snv | 1 | |||
rs11755527 | 0.851 | 0.360 | 6 | 90248512 | intron variant | C/G | snv | 0.36 | 5 | ||
rs11769828 | 1.000 | 0.200 | 7 | 150534221 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs11792633 | 0.882 | 0.280 | 9 | 6248035 | intron variant | C/T | snv | 0.35 | 5 | ||
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs12119179 | 0.925 | 0.200 | 1 | 67281732 | downstream gene variant | A/C | snv | 0.30 | 2 | ||
rs12141431 | 1.000 | 0.200 | 1 | 67281340 | downstream gene variant | G/C | snv | 0.23 | 1 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121908147 | 0.807 | 0.280 | 1 | 247424041 | missense variant | G/A;C | snv | 8.3E-03; 4.0E-06 | 7 | ||
rs12212193 | 0.925 | 0.280 | 6 | 90287050 | intron variant | A/G | snv | 0.38 | 2 | ||
rs1234313 | 0.807 | 0.400 | 1 | 173197108 | intron variant | A/G | snv | 0.72 | 6 | ||
rs1234315 | 0.807 | 0.400 | 1 | 173209324 | upstream gene variant | C/T | snv | 0.57 | 6 | ||
rs12569232 | 0.882 | 0.280 | 1 | 211379722 | intron variant | G/C;T | snv | 4 | |||
rs12785878 | 0.677 | 0.520 | 11 | 71456403 | intron variant | G/A;T | snv | 25 | |||
rs12932187 | 0.925 | 0.320 | 16 | 10878023 | intron variant | C/G;T | snv | 2 | |||
rs1310182 | 0.882 | 0.360 | 1 | 113830881 | intron variant | A/C;G | snv | 0.56 | 4 | ||
rs13154629 | 1.000 | 0.200 | 5 | 96786754 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
rs13210247 | 0.882 | 0.280 | 6 | 111601517 | non coding transcript exon variant | A/G | snv | 0.10 | 3 | ||
rs1327295035 | 1.000 | 0.200 | 6 | 52187730 | missense variant | A/G | snv | 1 | |||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 9 |