Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs2023239 | 0.724 | 0.160 | 6 | 88150763 | intron variant | T/C | snv | 0.21 | 20 | ||
rs806368 | 0.752 | 0.280 | 6 | 88140381 | 3 prime UTR variant | T/C | snv | 0.19 | 14 | ||
rs2609997 | 0.882 | 0.120 | 8 | 56447926 | intron variant | T/C | snv | 0.34 | 3 | ||
rs604300 | 1.000 | 0.080 | 3 | 127724009 | intron variant | A/G | snv | 0.91 | 3 | ||
rs1019238 | 0.925 | 0.080 | 17 | 56201354 | intron variant | G/A;C | snv | 2 | |||
rs1431318 | 0.925 | 0.080 | 17 | 56115162 | intron variant | A/G | snv | 0.64 | 2 | ||
rs806380 | 0.925 | 0.120 | 6 | 88154934 | intron variant | A/G | snv | 0.26 | 2 | ||
rs2576573 | 0.925 | 0.120 | 8 | 56445416 | 3 prime UTR variant | G/A | snv | 0.38 | 2 | ||
rs12491921 | 0.925 | 0.080 | 3 | 106570103 | intergenic variant | T/C | snv | 0.44 | 2 | ||
rs17664708 | 1.000 | 0.080 | 8 | 32579499 | intron variant | C/T | snv | 1.0E-01 | 2 | ||
rs7162140 | 1.000 | 0.080 | 15 | 34018399 | 5 prime UTR variant | C/G;T | snv | 0.15 | 1 |