Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10175368 | 0.925 | 0.080 | 2 | 38080719 | intron variant | C/T | snv | 0.23 | 4 | ||
rs10505346 | 0.925 | 0.080 | 8 | 118951604 | intron variant | G/T | snv | 0.22 | 4 | ||
rs13385191 | 0.925 | 0.080 | 2 | 20688505 | intron variant | A/G | snv | 0.20 | 4 | ||
rs17036508 | 0.925 | 0.080 | 1 | 11195977 | 3 prime UTR variant | T/C | snv | 9.0E-02 | 4 | ||
rs188140481 | 0.925 | 0.080 | 8 | 127179427 | non coding transcript exon variant | T/A;C | snv | 4 | |||
rs1983891 | 0.925 | 0.080 | 6 | 41568689 | intron variant | C/T | snv | 0.35 | 4 | ||
rs198977 | 0.925 | 0.080 | 19 | 50878521 | missense variant | C/T | snv | 0.24 | 0.30 | 4 | |
rs266882 | 0.925 | 0.080 | 19 | 50854757 | upstream gene variant | G/A | snv | 0.49 | 4 | ||
rs2705897 | 0.925 | 0.080 | 4 | 184631944 | splice region variant | T/G | snv | 0.64 | 0.73 | 4 | |
rs367590266 | 0.925 | 0.080 | 6 | 52797630 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 4 | |
rs368952331 | 0.925 | 0.080 | 15 | 74722805 | missense variant | C/T | snv | 2.8E-05 | 6.3E-05 | 4 | |
rs4647603 | 0.925 | 0.080 | 4 | 184648576 | 5 prime UTR variant | C/T | snv | 0.11 | 4 | ||
rs6983269 | 0.925 | 0.080 | 8 | 2741967 | intron variant | C/A;G;T | snv | 0.42 | 4 | ||
rs775220785 | 0.925 | 0.080 | 7 | 99772615 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
rs780354238 | 0.925 | 0.080 | 8 | 42369855 | missense variant | A/G | snv | 4.4E-06 | 4 | ||
rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
rs12653946 | 0.882 | 0.080 | 5 | 1895715 | intron variant | C/T | snv | 0.43 | 5 | ||
rs406193 | 0.882 | 0.120 | 20 | 32811837 | downstream gene variant | T/C | snv | 0.91 | 5 | ||
rs4919743 | 0.925 | 0.080 | 12 | 52915800 | intron variant | G/A | snv | 0.13 | 5 | ||
rs6504074 | 0.882 | 0.120 | 17 | 61822429 | intron variant | G/A;T | snv | 5 | |||
rs7008482 | 0.882 | 0.120 | 8 | 125255388 | intron variant | T/G | snv | 0.48 | 5 | ||
rs7254617 | 0.882 | 0.120 | 19 | 40285605 | upstream gene variant | G/A;C;T | snv | 5 | |||
rs9600079 | 0.925 | 0.080 | 13 | 73154002 | intergenic variant | G/T | snv | 0.46 | 5 | ||
rs10896449 | 0.827 | 0.200 | 11 | 69227200 | intergenic variant | A/G | snv | 0.53 | 6 | ||
rs1469713 | 0.827 | 0.160 | 19 | 19417997 | intron variant | A/G | snv | 0.44 | 6 |