Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 4
rs34234989
MMP24-AS1-EDEM2 ; PROCR
0.882 0.120 20 35186731 intron variant A/- delins 0.40 5
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs9411377
ABO
9 133269992 intron variant A/C snv 0.62 2
rs115865014
TBC1D5 ; SATB1
3 18424258 5 prime UTR variant A/C snv 1.2E-02 1
rs149130695
F11-AS1
4 186464194 intron variant A/C snv 5.0E-02 1
rs149328960
LINC02476
7 119612310 intron variant A/C snv 0.12 1
rs16861990
NME7
1 169165889 intron variant A/C snv 5.5E-02 1
rs9880479 3 39195984 upstream gene variant A/C;G snv 1
rs4253421
F11
4 186283783 intron variant A/C;G;T snv 2
rs7297265
COPZ1
12 54325905 intron variant A/C;G;T snv 1
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 6
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 4
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 4
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 3
rs10498632
TC2N
14 91824400 intron variant A/G snv 0.29 2
rs1409338
PLXDC2
10 19938338 intron variant A/G snv 0.75 2
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 2
rs4734879
ZFPM2-AS1 ; ZFPM2
8 105570896 intron variant A/G snv 0.31 2
rs1018827
F5
1 169544768 intron variant A/G snv 0.92 1
rs12122803
C1orf112
1 169825364 intron variant A/G snv 1.4E-02 1