Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10776934 | 1.000 | 0.080 | 9 | 135137855 | regulatory region variant | T/G | snv | 0.74 | 1 | ||
rs11966728 | 1.000 | 0.080 | 6 | 131955465 | intron variant | T/C | snv | 0.26 | 1 | ||
rs12972991 | 1.000 | 0.080 | 19 | 39241107 | upstream gene variant | A/C | snv | 0.19 | 1 | ||
rs12980602 | 1.000 | 0.080 | 19 | 39262180 | upstream gene variant | T/C | snv | 0.25 | 1 | ||
rs4803223 | 1.000 | 0.080 | 19 | 39255579 | upstream gene variant | A/G | snv | 0.13 | 1 | ||
rs8109886 | 1.000 | 0.080 | 19 | 39252122 | upstream gene variant | C/A | snv | 0.53 | 1 | ||
rs965469 | 1.000 | 0.080 | 20 | 3400902 | intron variant | T/C | snv | 0.20 | 1 | ||
rs11697186 | 1.000 | 0.080 | 20 | 3204477 | intron variant | A/C;T | snv | 7.0E-02 | 1 | ||
rs10789491 | 1.000 | 0.080 | 1 | 46713638 | intron variant | A/G | snv | 0.80 | 1 | ||
rs28416813 | 1.000 | 0.080 | 19 | 39245004 | 5 prime UTR variant | C/G | snv | 0.31 | 0.39 | 1 | |
rs6139030 | 1.000 | 0.080 | 20 | 3207087 | upstream gene variant | T/C | snv | 8.6E-02 | 1 | ||
rs12952093 | 1.000 | 0.080 | 17 | 78367559 | intron variant | A/C;T | snv | 1 | |||
rs1293762 | 1.000 | 0.080 | 12 | 112993031 | intron variant | T/G | snv | 0.67 | 1 | ||
rs2779180 | 1.000 | 0.080 | 19 | 4841139 | intron variant | A/G | snv | 0.37 | 1 | ||
rs1470452230 | 0.925 | 0.120 | 9 | 135561895 | missense variant | A/C | snv | 7.0E-06 | 2 | ||
rs12989760 | 0.925 | 0.120 | 2 | 250470 | intron variant | T/C | snv | 2 | |||
rs11854484 | 0.925 | 0.120 | 15 | 45253280 | missense variant | C/T | snv | 0.47 | 0.45 | 2 | |
rs6051702 | 0.882 | 0.120 | 20 | 3271278 | intron variant | A/C | snv | 0.19 | 3 | ||
rs2230201 | 0.882 | 0.200 | 19 | 6713280 | synonymous variant | C/G;T | snv | 0.19 | 3 | ||
rs1863918 | 0.882 | 0.160 | 5 | 179112381 | 3 prime UTR variant | G/T | snv | 0.25 | 4 | ||
rs2267716 | 0.851 | 0.120 | 7 | 30677027 | intron variant | T/A;C | snv | 4 | |||
rs9695310 | 0.851 | 0.120 | 9 | 32464137 | intron variant | G/C | snv | 0.52 | 4 | ||
rs11506105 | 0.851 | 0.160 | 7 | 55152484 | intron variant | A/G | snv | 0.59 | 4 | ||
rs4803217 | 0.882 | 0.120 | 19 | 39243580 | 3 prime UTR variant | C/A | snv | 0.39 | 4 | ||
rs8103142 | 0.882 | 0.120 | 19 | 39244466 | missense variant | T/C | snv | 0.29 | 0.40 | 4 |