Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9998811
SLC2A9
0.925 0.120 4 9964853 intron variant G/A snv 0.24 3
rs9998739
SLC2A9 ; LOC105374476
0.925 0.120 4 9994885 intron variant G/A snv 0.23 3
rs9998663 0.925 0.120 4 9625429 intron variant C/A;T snv 2
rs9996284 0.925 0.120 4 10467822 intron variant C/G snv 0.40 3
rs9994266
SLC2A9
0.925 0.120 4 9952826 intron variant G/A snv 0.49 3
rs9994202
CLNK
0.925 0.120 4 10557772 intron variant T/A;C;G snv 2
rs9993652
SLC2A9
0.925 0.120 4 9887225 intron variant G/A;C;T snv 3
rs9993410
SLC2A9
0.925 0.120 4 9949640 intron variant C/T snv 0.50 3
rs9992406
SLC2A9
0.925 0.120 4 9984664 intron variant C/A;T snv 0.23 3
rs9991653 0.925 0.120 4 10308871 intergenic variant A/G snv 0.44 3
rs9991278
SLC2A9 ; LOC105374476
0.925 0.120 4 10001041 intron variant T/A;C snv 3
rs9990701 0.925 0.120 4 10386986 intergenic variant A/G;T snv 3
rs9990501 0.925 0.120 4 10202969 upstream gene variant A/G snv 0.66 3
rs9990427 0.925 0.120 4 10386689 intergenic variant A/G;T snv 2
rs998676
SLC2A9
0.925 0.120 4 9946940 intron variant T/A;C snv 3
rs998675
SLC2A9
0.925 0.120 4 9947205 intron variant C/T snv 0.58 3
rs997630 0.925 0.120 4 88242701 intergenic variant A/G snv 0.42 2
rs997219
CLNK ; LOC105374482
0.925 0.120 4 10523047 intron variant G/A snv 0.46 3
rs9952962 0.925 0.120 18 29955603 intergenic variant T/C snv 0.70 2
rs993173 0.925 0.120 4 10322311 intergenic variant T/C snv 0.44 3
rs993172 0.925 0.120 4 10322737 intergenic variant A/C snv 0.44 3
rs9926
WDR1
0.925 0.120 4 10075236 3 prime UTR variant G/A snv 0.17 3
rs991458 0.925 0.120 4 10307132 intergenic variant C/T snv 0.77 2
rs9905274
BCAS3
0.925 0.120 17 61373080 intron variant T/A;C snv 3
rs9900205
PRKCA
0.925 0.120 17 66718990 intron variant A/C;T snv 2