Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs3130361 | 0.925 | 0.160 | 6 | 30371787 | intergenic variant | A/G | snv | 0.81 | 3 | ||
rs2508015 | 0.925 | 0.160 | 6 | 31042423 | regulatory region variant | G/A;C | snv | 2 | |||
rs2523535 | 0.851 | 0.200 | 6 | 31368473 | intron variant | A/G | snv | 0.32 | 7 | ||
rs492899 | 0.882 | 0.240 | 6 | 31965741 | intron variant | T/C | snv | 0.12 | 0.15 | 2 | |
rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 12 | ||
rs12663103 | 0.851 | 0.240 | 6 | 32193547 | intron variant | T/C | snv | 6.1E-02 | 7 | ||
rs2395174 | 0.827 | 0.320 | 6 | 32437101 | upstream gene variant | T/G | snv | 0.24 | 5 | ||
rs3892710 | 0.851 | 0.240 | 6 | 32715085 | upstream gene variant | C/T | snv | 0.22 | 4 | ||
rs9276991 | 0.882 | 0.240 | 6 | 33014071 | upstream gene variant | A/G | snv | 6.0E-02 | 3 | ||
rs423639 | 0.882 | 0.240 | 6 | 33019997 | intergenic variant | C/T | snv | 0.11 | 3 |