Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 4
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 4
rs1801690
APOH
0.925 0.120 17 66212167 missense variant C/G snv 4.8E-02 4.0E-02 3
rs2545801
GRK6
5 177414338 intron variant T/C snv 0.56 3
rs4253421
F11
4 186283783 intron variant A/C;G;T snv 2
rs2289252
F11-AS1 ; F11
1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35 2
rs1042445
HRG ; LOC105374258
3 186677647 missense variant C/A;T snv 0.27 2
rs7447593
SLC34A1
5 177397136 non coding transcript exon variant C/G;T snv 2
rs12644950 4 154616169 upstream gene variant G/A snv 0.25 1
rs2469184
AGBL1
15 86648746 intron variant A/G snv 0.54 1
rs7962629
C1S
12 7059466 intron variant A/G snv 0.13 1
rs1593
F11
4 186274397 3 prime UTR variant T/A;G snv 1
rs56810541
F11
4 186279396 intron variant A/T snv 0.35 1
rs6013
F5
1 169518583 intron variant G/A;T snv 2.6E-04; 6.4E-02 1
rs6028
F5
1 169582444 synonymous variant T/C snv 0.29 0.23 1
rs16860992
HRG ; LOC105374258
1.000 0.080 3 186676249 intron variant G/C;T snv 1
rs9898
HRG ; LOC105374258
0.925 0.160 3 186672838 missense variant C/T snv 0.38 0.43 1
rs4253276
KLKB1
4 186242705 intron variant G/C snv 5.3E-02 1
rs5030081
KNG1
3 186741121 intron variant G/A snv 0.43 1
rs710446
KNG1
0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44 1