Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
rs104893878 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 21 | |||
rs1289324472 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 21 | ||
rs4606 | 0.752 | 0.120 | 1 | 192812042 | 3 prime UTR variant | C/G;T | snv | 16 | |||
rs63751438 | 0.776 | 0.120 | 17 | 46010388 | missense variant | C/T | snv | 16 | |||
rs1555507479 | 0.807 | 0.160 | 16 | 56336799 | missense variant | C/A | snv | 12 | |||
rs242557 | 0.752 | 0.200 | 17 | 45942346 | intron variant | G/A | snv | 0.36 | 12 | ||
rs113994099 | 0.827 | 0.240 | 15 | 89320883 | missense variant | T/C | snv | 10 | |||
rs63750590 | 0.790 | 0.120 | 14 | 73186860 | missense variant | A/G | snv | 10 | |||
rs188286943 | 0.776 | 0.160 | 16 | 46662452 | missense variant | C/T | snv | 9 | |||
rs63750522 | 0.827 | 0.120 | 14 | 73173644 | missense variant | G/A;C | snv | 8 | |||
rs63750577 | 0.827 | 0.120 | 14 | 73186881 | missense variant | C/T | snv | 8 | |||
rs34995376 | 0.807 | 0.080 | 12 | 40310435 | missense variant | G/A | snv | 7.0E-06 | 7 | ||
rs35801418 | 0.827 | 0.120 | 12 | 40321114 | missense variant | A/G | snv | 7 | |||
rs63750416 | 0.851 | 0.120 | 17 | 46010373 | missense variant | A/C | snv | 7 | |||
rs63750802 | 0.851 | 0.080 | 14 | 73219144 | missense variant | T/G | snv | 7 | |||
rs63751032 | 0.851 | 0.080 | 14 | 73219156 | missense variant | T/A;G | snv | 7 | |||
rs1224426272 | 0.925 | 0.040 | 12 | 119869138 | missense variant | C/T | snv | 6 | |||
rs3135500 | 0.851 | 0.160 | 16 | 50732975 | 3 prime UTR variant | G/A | snv | 0.44 | 5 | ||
rs63750050 | 0.925 | 0.080 | 14 | 73198106 | missense variant | T/G | snv | 5 | |||
rs2942168 | 0.925 | 0.120 | 17 | 45637484 | non coding transcript exon variant | G/A;C;T | snv | 0.14 | 4 | ||
rs63750444 | 0.882 | 0.080 | 14 | 73192745 | missense variant | G/A | snv | 4 | |||
rs886039227 | 0.925 | 0.200 | 2 | 74378123 | missense variant | A/C | snv | 4 | |||
rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 3 |