Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2303425
MSH2
0.790 0.120 2 47403074 5 prime UTR variant T/C snv 0.10 8
rs3104746
CASC16
0.790 0.120 16 52567188 intron variant T/A snv 8.6E-02 7
rs4442975
LOC101928278
0.827 0.120 2 217056046 intergenic variant G/T snv 0.47 7
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs9485372
TAB2
0.807 0.120 6 149287738 intron variant G/A snv 0.20 6
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins 4
rs1416532705
ERBB2
0.882 0.080 17 39709435 missense variant C/T snv 4.0E-06 3
rs4593472
LINC-PINT
0.882 0.080 7 130982362 intron variant C/T snv 0.31 3
rs6099128
AURKA
0.925 20 56390288 intron variant T/G snv 0.13 2