Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs1991517 | 0.752 | 0.240 | 14 | 81144239 | missense variant | G/C | snv | 0.90 | 0.91 | 13 | |
rs17879469 | 0.763 | 0.360 | 6 | 32584333 | missense variant | C/G | snv | 1.3E-05 | 9 | ||
rs3789604 | 0.776 | 0.360 | 1 | 113812320 | synonymous variant | T/A;C;G | snv | 8.5E-06; 1.3E-05; 0.17 | 9 | ||
rs121908873 | 0.790 | 0.160 | 14 | 81139828 | missense variant | G/A;T | snv | 7 | |||
rs121908874 | 0.807 | 0.080 | 14 | 81143584 | missense variant | T/C | snv | 7 | |||
rs4416670 | 0.827 | 0.240 | 6 | 43982716 | intergenic variant | T/C | snv | 0.45 | 7 | ||
rs3827440 | 0.851 | 0.120 | X | 79171491 | missense variant | T/A;C | snv | 5.5E-06; 0.51 | 6 | ||
rs2046045 | 0.925 | 0.080 | 5 | 77239986 | intron variant | T/C;G | snv | 4 | |||
rs28937584 | 0.925 | 0.080 | 14 | 81143955 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
rs12138950 | 0.925 | 0.040 | 1 | 19512621 | intron variant | A/C | snv | 5.4E-03 | 3 | ||
rs1311839715 | 0.882 | 0.200 | 17 | 21703291 | missense variant | G/C | snv | 7.0E-06 | 3 | ||
rs571893270 | 0.882 | 0.040 | 14 | 81143641 | missense variant | G/A | snv | 8.0E-05 | 2.1E-05 | 3 | |
rs9355610 | 0.882 | 0.200 | 6 | 166969587 | downstream gene variant | G/A;T | snv | 3 | |||
rs118039499 | 1.000 | 0.040 | 8 | 132759389 | 5 prime UTR variant | A/C | snv | 1.4E-02 | 2 | ||
rs121908875 | 0.925 | 0.040 | 14 | 81144073 | missense variant | G/A | snv | 2 | |||
rs121908879 | 0.925 | 0.080 | 14 | 81096641 | missense variant | A/G | snv | 2 | |||
rs12722039 | 0.925 | 0.120 | 6 | 32637507 | missense variant | G/A | snv | 5.7E-02 | 8.4E-02 | 2 | |
rs1482760341 | 0.925 | 0.120 | 21 | 31668548 | missense variant | G/C;T | snv | 1.6E-05 | 2 | ||
rs2983514 | 0.925 | 0.040 | 6 | 165636631 | intron variant | A/G | snv | 0.34 | 2 | ||
rs925488 | 1.000 | 0.040 | 9 | 97784109 | intron variant | G/A | snv | 0.71 | 2 | ||
rs11038357 | 1.000 | 0.040 | 11 | 45216307 | intron variant | T/A;G | snv | 1 | |||
rs17477923 | 1.000 | 0.040 | 15 | 49418988 | intron variant | T/C | snv | 0.22 | 1 |