Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587781960 | 0.882 | 0.080 | 22 | 28689164 | missense variant | A/C;G;T | snv | 1.3E-05; 7.3E-05 | 4 | ||
rs6776706 | 0.851 | 0.080 | 3 | 25439731 | intron variant | T/A | snv | 0.27 | 4 | ||
rs749098599 | 0.882 | 0.080 | 1 | 3683085 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 4 | |
rs780294601 | 0.851 | 0.080 | 3 | 12416967 | missense variant | G/C | snv | 4.4E-05 | 1.4E-05 | 4 | |
rs781734330 | 0.851 | 0.080 | 1 | 16995981 | missense variant | C/T | snv | 4 | |||
rs10055201 | 0.882 | 0.080 | 5 | 55865274 | intron variant | A/G | snv | 0.76 | 3 | ||
rs1027702 | 0.882 | 0.080 | 1 | 161743067 | intergenic variant | C/T | snv | 0.51 | 3 | ||
rs10840002 | 0.882 | 0.080 | 11 | 8221479 | downstream gene variant | A/G | snv | 0.49 | 3 | ||
rs110420 | 0.882 | 0.080 | 11 | 8231502 | intron variant | T/C | snv | 0.42 | 3 | ||
rs11247957 | 0.882 | 0.080 | 1 | 26429683 | 3 prime UTR variant | G/A | snv | 0.21 | 3 | ||
rs1211164799 | 0.882 | 0.080 | 17 | 49973938 | missense variant | A/T | snv | 3 | |||
rs12442054 | 0.882 | 0.080 | 15 | 74165683 | intron variant | G/A | snv | 0.12 | 3 | ||
rs1273925499 | 0.882 | 0.080 | 17 | 45991557 | missense variant | C/G;T | snv | 4.0E-06 | 3 | ||
rs1301478248 | 0.882 | 0.080 | 1 | 15495395 | missense variant | C/T | snv | 3 | |||
rs13034994 | 0.882 | 0.080 | 2 | 15938513 | non coding transcript exon variant | A/C;G | snv | 3 | |||
rs138085133 | 0.882 | 0.080 | 1 | 26022729 | missense variant | C/G;T | snv | 8.4E-04; 4.0E-06 | 3 | ||
rs1415224147 | 0.882 | 0.080 | 9 | 125585715 | missense variant | T/C | snv | 3 | |||
rs143864187 | 0.882 | 0.080 | 11 | 104949666 | missense variant | C/A | snv | 3 | |||
rs1442511697 | 0.882 | 0.080 | 2 | 96115494 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
rs145976111 | 0.882 | 0.080 | 17 | 75742728 | missense variant | C/T | snv | 2.9E-03 | 2.3E-03 | 3 | |
rs147480547 | 0.882 | 0.080 | 17 | 75740047 | missense variant | G/A;T | snv | 1.1E-03; 4.0E-06 | 3 | ||
rs147992979 | 0.882 | 0.080 | 15 | 88184270 | missense variant | G/A | snv | 8.0E-05 | 4.4E-05 | 3 | |
rs17065417 | 0.882 | 0.080 | 6 | 104958399 | intron variant | A/C | snv | 0.10 | 3 | ||
rs17487792 | 0.882 | 0.080 | 2 | 214778776 | intron variant | C/T | snv | 0.16 | 3 | ||
rs17489363 | 0.882 | 0.080 | 2 | 214809617 | 5 prime UTR variant | A/G | snv | 0.73 | 0.74 | 3 |