Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 16 | |
rs9264942 | 0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 | 15 | ||
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 11 | ||
rs241447 | 0.827 | 0.280 | 6 | 32828974 | missense variant | T/C | snv | 0.31 | 0.26 | 11 | |
rs2229116 | 0.827 | 0.080 | 15 | 33613209 | missense variant | A/G | snv | 0.23 | 0.21 | 9 | |
rs1015164 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 8 | ||||
rs11157436 | 0.851 | 0.040 | 14 | 22168978 | synonymous variant | C/T | snv | 0.19 | 7 | ||
rs10808739 | 0.882 | 8 | 64727703 | intron variant | G/A | snv | 0.24 | 6 | |||
rs11790131 | 0.882 | 0.080 | 9 | 19469848 | intergenic variant | G/A;T | snv | 6 | |||
rs143633948 | 0.882 | 0.080 | 6 | 131504454 | intron variant | G/A;C | snv | 6 | |||
rs2442719 | 0.882 | 0.120 | 6 | 31352761 | intron variant | C/T | snv | 0.53 | 6 | ||
rs35467001 | 0.882 | 0.080 | 17 | 73383923 | missense variant | G/A | snv | 5.3E-02 | 6.3E-02 | 6 | |
rs35897606 | 0.882 | 0.080 | 11 | 33436311 | intron variant | A/G | snv | 4.4E-02 | 6 | ||
rs73084982 | 0.882 | 0.080 | 20 | 3430406 | intergenic variant | G/A | snv | 3.5E-02 | 6 | ||
rs73132848 | 0.882 | 0.080 | 3 | 8764738 | intron variant | G/A | snv | 9.3E-02 | 6 | ||
rs79709413 | 0.882 | 0.080 | 13 | 24740488 | upstream gene variant | G/T | snv | 4.7E-02 | 6 | ||
rs10892324 | 0.925 | 11 | 119032329 | upstream gene variant | T/A;G | snv | 5 | ||||
rs11231017 | 0.925 | 11 | 62293877 | downstream gene variant | G/A | snv | 0.29 | 5 | |||
rs11649112 | 0.925 | 16 | 13267554 | intron variant | G/A | snv | 0.22 | 5 | |||
rs12460243 | 0.925 | 19 | 8066356 | intron variant | G/A | snv | 0.14 | 5 | |||
rs13064773 | 0.925 | 3 | 158893105 | intergenic variant | G/A | snv | 0.39 | 5 | |||
rs16823858 | 0.925 | 3 | 115559835 | intron variant | G/A;C | snv | 5 | ||||
rs16933829 | 0.925 | 11 | 17094129 | intron variant | T/C | snv | 6.2E-02 | 5 | |||
rs17038463 | 0.925 | 3 | 1383484 | intron variant | T/C;G | snv | 5 | ||||
rs17151904 | 0.925 | 7 | 25568789 | TF binding site variant | G/A;C | snv | 5 |