Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782477
APC
0.882 0.120 5 112775679 missense variant A/T snv 4
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs7309123
LOC105369655 ; CLEC7A
0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs74597325
CFTR
0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs796051877
GAA
0.807 0.320 17 80110055 splice region variant G/A snv 4.0E-06 11
rs868435969
VCP
0.925 0.280 9 35066710 missense variant G/A snv 3
rs879253740
NPC2 ; ISCA2
0.882 0.240 14 74493191 splice donor variant A/G snv 5