Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591741
CHUK
1.000 0.080 10 100216744 intron variant G/C snv 0.30 1
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs78900934 1.000 0.080 1 101272565 upstream gene variant C/A snv 0.32 1
rs6598475
PCSK6
1.000 0.080 15 101446425 intron variant G/T snv 0.63 1
rs6543087
MAP4K4
1.000 0.080 2 101699471 intron variant A/G;T snv 1
rs117168171 1.000 0.080 15 101854599 downstream gene variant C/G;T snv 2
rs2607653
FGF14
1.000 0.080 13 102066314 intron variant A/G snv 5.9E-02 2
rs2548724
SLCO4C1
1.000 0.080 5 102284470 intron variant T/C snv 0.81 1
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 3
rs4729854
RASA4DP
1.000 0.080 7 102743216 intron variant T/A snv 0.35 1
rs7729395
PAM
1.000 0.080 5 102764872 intron variant C/T snv 3.1E-02 2
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs72783884
PAM
1.000 0.080 5 102912212 intron variant A/T snv 6.8E-03 1
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 2
rs78408340
PAM
1.000 0.080 5 103003035 missense variant C/G;T snv 3.7E-03; 8.1E-06 2
rs35658696
PAM
1.000 0.080 5 103003107 missense variant A/G snv 3.1E-02 3.2E-02 3
rs7674212
SLC9B2
1.000 0.080 4 103067742 intron variant G/A;T snv 1
rs115505614
GIN1
1.000 0.080 5 103087264 3 prime UTR variant C/T snv 3.2E-02 1
rs75432112 1.000 0.080 5 103250706 intron variant G/A snv 3.0E-02 1
rs2299383
RELN
1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs13268287
LRP12
1.000 0.080 8 104548593 intron variant A/G snv 1.6E-02 1