Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10974438 | 0.925 | 0.120 | 9 | 4291928 | intron variant | A/C | snv | 0.29 | 3 | ||
rs11591710 | 0.882 | 0.160 | 10 | 103927874 | intergenic variant | A/C | snv | 0.16 | 3 | ||
rs1372503923 | 0.925 | 0.160 | 5 | 53048731 | missense variant | A/C | snv | 3 | |||
rs16860234 | 0.925 | 0.080 | 3 | 185793096 | intron variant | A/C | snv | 0.33 | 3 | ||
rs2275703 | 0.925 | 0.080 | 1 | 160195305 | intron variant | A/C | snv | 0.38 | 3 | ||
rs9896052 | 0.882 | 0.160 | 17 | 75422781 | intergenic variant | A/C | snv | 0.50 | 3 | ||
rs10517030 | 0.925 | 0.120 | 4 | 23961283 | intergenic variant | A/C | snv | 6.9E-02 | 2 | ||
rs115689251 | 1.000 | 0.080 | 17 | 36032377 | intergenic variant | A/C | snv | 1.0E-02 | 2 | ||
rs118204073 | 0.925 | 0.120 | 8 | 19951825 | missense variant | A/C | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs11873305 | 1.000 | 0.080 | 18 | 60381959 | intron variant | A/C | snv | 0.12 | 2 | ||
rs151290 | 1.000 | 0.080 | 11 | 2800385 | intron variant | A/C | snv | 0.67 | 2 | ||
rs1541276 | 0.925 | 0.120 | 18 | 13825728 | splice region variant | A/C | snv | 0.17 | 0.19 | 2 | |
rs75298135 | 1.000 | 0.080 | 5 | 28184372 | intergenic variant | A/C | snv | 1.3E-02 | 2 | ||
rs7929543 | 0.925 | 0.120 | 11 | 49329474 | intron variant | A/C | snv | 0.12 | 2 | ||
rs9472719 | 1.000 | 0.080 | 6 | 46183649 | regulatory region variant | A/C | snv | 0.32 | 2 | ||
rs9942471 | 0.925 | 0.160 | 6 | 89238513 | intergenic variant | A/C | snv | 0.37 | 2 | ||
rs10100265 | 1.000 | 0.080 | 8 | 10775649 | intron variant | A/C | snv | 0.60 | 1 | ||
rs1071592 | 1.000 | 0.080 | 3 | 186620636 | synonymous variant | A/C | snv | 0.76 | 0.77 | 1 | |
rs13083654 | 1.000 | 0.080 | 3 | 23245193 | intron variant | A/C | snv | 0.11 | 1 | ||
rs141205818 | 1.000 | 0.080 | 3 | 186854691 | missense variant | A/C | snv | 3.9E-04 | 1.8E-04 | 1 | |
rs1424642 | 1.000 | 0.080 | 2 | 57069423 | intergenic variant | A/C | snv | 0.78 | 1 | ||
rs16856187 | 1.000 | 0.080 | 2 | 168913876 | upstream gene variant | A/C | snv | 6.0E-02 | 1 | ||
rs202178099 | 1.000 | 0.080 | 5 | 50927276 | downstream gene variant | A/C | snv | 3.2E-02 | 1 | ||
rs2283228 | 1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 | 1 | ||
rs2779772 | 1.000 | 0.080 | 9 | 17147193 | intron variant | A/C | snv | 0.21 | 1 |