Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 34 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 15 | ||
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 12 | ||
rs1111875 | 0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 | 10 | ||
rs1387153 | 0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv | 10 | |||
rs5015480 | 0.851 | 0.120 | 10 | 92705802 | downstream gene variant | C/T | snv | 0.42 | 9 | ||
rs744373 | 0.851 | 0.160 | 2 | 127137039 | downstream gene variant | A/G | snv | 0.35 | 8 | ||
rs7923837 | 0.882 | 0.160 | 10 | 92722160 | intergenic variant | G/A;T | snv | 8 | |||
rs10830962 | 0.851 | 0.160 | 11 | 92965261 | upstream gene variant | C/A;G;T | snv | 7 | |||
rs10804591 | 3 | 129615390 | intergenic variant | C/A | snv | 0.63 | 5 | ||||
rs12779790 | 0.882 | 0.120 | 10 | 12286011 | intergenic variant | A/G | snv | 0.17 | 5 | ||
rs2383208 | 0.882 | 0.120 | 9 | 22132077 | downstream gene variant | A/G;T | snv | 0.18 | 5 | ||
rs6681231 | 0.882 | 0.120 | 1 | 186690727 | intergenic variant | G/C | snv | 0.22 | 5 | ||
rs7936247 | 1.000 | 0.040 | 11 | 92956866 | intergenic variant | G/T | snv | 0.37 | 5 | ||
rs10245353 | 7 | 25818994 | intergenic variant | C/A | snv | 0.16 | 4 | ||||
rs10229583 | 1.000 | 0.080 | 7 | 127606849 | downstream gene variant | G/A | snv | 0.23 | 2 | ||
rs275645 | 3 | 148746667 | downstream gene variant | G/A | snv | 0.43 | 1 | ||||
rs137852671 | 0.790 | 0.160 | 11 | 17394295 | missense variant | C/T | snv | 10 | |||
rs909221872 | 1 | 6349856 | missense variant | G/T | snv | 1 | |||||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 9 | ||
rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 | ||
rs3750625 | 10 | 111079843 | 3 prime UTR variant | C/A | snv | 8.7E-02 | 2 |