Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 9
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8