Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10919791 | 0.925 | 0.240 | 1 | 199996040 | intergenic variant | G/A | snv | 0.22 | 1 | ||
rs2816938 | 1.000 | 0.120 | 1 | 200016240 | upstream gene variant | T/A | snv | 0.37 | 1 | ||
rs9363918 | 0.882 | 0.200 | 6 | 68432116 | intron variant | T/G | snv | 0.38 | 1 | ||
rs10094872 | 0.882 | 0.200 | 8 | 127707639 | intron variant | A/T | snv | 0.33 | 1 | ||
rs372266620 | 0.925 | 0.120 | 9 | 21971189 | missense variant | G/A;C;T | snv | 9.1E-05; 2.3E-05; 9.1E-06 | 1 | ||
rs4269383 | 0.882 | 0.120 | 6 | 155876368 | intergenic variant | A/G | snv | 0.37 | 1 | ||
rs876493 | 0.925 | 0.160 | 17 | 39668292 | intron variant | G/A | snv | 0.47 | 1 | ||
rs375328708 | 1.000 | 0.120 | 19 | 1226602 | synonymous variant | C/G;T | snv | 6.7E-05 | 6.3E-05 | 1 | |
rs35226131 | 1.000 | 0.120 | 5 | 1295258 | upstream gene variant | C/T | snv | 2.6E-02 | 1 | ||
rs9854771 | 0.925 | 0.240 | 3 | 189790682 | intron variant | G/A | snv | 0.34 | 1 | ||
rs10887710 | 0.925 | 0.120 | 10 | 80270029 | downstream gene variant | T/C | snv | 0.19 | 2 | ||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 2 | ||
rs1517037 | 0.882 | 0.120 | 18 | 59211042 | intergenic variant | C/T | snv | 0.23 | 2 | ||
rs1552462 | 0.925 | 0.120 | 11 | 7235910 | upstream gene variant | C/T | snv | 2.7E-02 | 2 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 2 | ||
rs6001516 | 0.925 | 0.120 | 22 | 39248198 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs11644043 | 0.925 | 0.120 | 16 | 50327466 | intron variant | T/C | snv | 0.24 | 2 | ||
rs782128510 | 0.925 | 0.120 | 17 | 410373 | missense variant | C/A;G | snv | 7.6E-05; 8.4E-06 | 2 | ||
rs1276300653 | 0.925 | 0.120 | 3 | 9757072 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
rs1800843 | 0.925 | 0.120 | 11 | 6270835 | synonymous variant | C/A;G | snv | 0.16; 4.0E-06 | 0.19 | 2 | |
rs1336539869 | 0.925 | 0.120 | 12 | 57751681 | missense variant | C/G | snv | 2 | |||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 2 | ||
rs1339638227 | 0.925 | 0.120 | 9 | 21971119 | missense variant | T/C | snv | 4.3E-06 | 2 | ||
rs1537373 | 0.925 | 0.120 | 9 | 22103342 | intron variant | T/G | snv | 0.63 | 2 | ||
rs6475609 | 0.925 | 0.120 | 9 | 22106272 | intron variant | A/C;G;T | snv | 2 |