Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 18 | |||
rs2855812 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 13 | ||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 12 | ||
rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 11 | ||
rs11172113 | 0.882 | 0.080 | 12 | 57133500 | intron variant | T/C | snv | 0.42 | 10 | ||
rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 10 | ||
rs2857595 | 0.827 | 0.320 | 6 | 31600692 | intergenic variant | G/A | snv | 0.27 | 9 | ||
rs12504628 | 1.000 | 0.040 | 4 | 144515172 | intron variant | T/C | snv | 0.33 | 6 | ||
rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 6 | |||
rs1980057 | 1.000 | 0.040 | 4 | 144564586 | intron variant | C/T | snv | 0.31 | 6 | ||
rs2284746 | 1 | 16980180 | intron variant | C/A;G | snv | 6 | |||||
rs13147758 | 4 | 144539078 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs1541374 | 4 | 105127203 | intergenic variant | T/A;G | snv | 5 | |||||
rs2798641 | 6 | 108946847 | intron variant | C/T | snv | 0.15 | 5 | ||||
rs2865531 | 1.000 | 0.040 | 16 | 75356418 | intron variant | T/A | snv | 0.52 | 5 | ||
rs3995090 | 1.000 | 0.040 | 5 | 148466252 | intron variant | A/C | snv | 0.39 | 5 | ||
rs7068966 | 1.000 | 0.040 | 10 | 12235993 | intron variant | C/T | snv | 0.43 | 5 | ||
rs7733088 | 1.000 | 0.040 | 5 | 148476770 | intron variant | G/A;C | snv | 0.44; 4.1E-06 | 5 | ||
rs1036429 | 12 | 95877650 | intron variant | T/C | snv | 0.79 | 4 | ||||
rs10516526 | 4 | 105767747 | intron variant | A/G | snv | 5.4E-02 | 4 | ||||
rs11001819 | 10 | 76555466 | intron variant | G/A | snv | 0.41 | 4 | ||||
rs11168048 | 5 | 148462790 | intron variant | T/C | snv | 0.38 | 4 | ||||
rs11727189 | 4 | 105697983 | intron variant | G/T | snv | 5.4E-02 | 4 | ||||
rs12447804 | 16 | 58041378 | intron variant | C/T | snv | 0.18 | 4 |