Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64 4
rs4642
ITGB3
1.000 0.080 17 47292411 synonymous variant A/G snv 0.29 0.29 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs8176732
ABO
9 133256916 intron variant A/G snv 0.25 3
rs1018827
F5
1 169544768 intron variant A/G snv 0.92 2
rs10498632
TC2N
14 91824400 intron variant A/G snv 0.29 2
rs10737547 1 169506814 intergenic variant A/G snv 0.93 2
rs1409338
PLXDC2
10 19938338 intron variant A/G snv 0.75 2
rs2420372
F5
1 169528818 intron variant A/G snv 0.95 2
rs3756009
F11
4 186264957 upstream gene variant A/G snv 0.32 2
rs4734879
ZFPM2-AS1 ; ZFPM2
8 105570896 intron variant A/G snv 0.31 2
rs6048
F9
1.000 0.040 X 139551121 missense variant A/G snv 0.22 0.23 2
rs6696217 1 169491488 non coding transcript exon variant A/G snv 0.92 2
rs780225764
F2
1.000 0.080 11 46726797 missense variant A/G snv 4.0E-06 2