Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 9
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs5860563
ADH4 ; LOC100507053
1.000 0.080 4 99126006 intron variant -/A delins 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs143558304
TPM4
19 16102887 3 prime UTR variant -/A delins 4.6E-02 2
rs140348140
KIAA2026
9 5877295 downstream gene variant -/A delins 3.1E-02 2
rs397948882 0.925 0.040 7 15597253 intergenic variant -/A delins 2.9E-04 2
rs71297631
TEX9
15 56369974 intron variant -/A ins 2
rs142530265
GNAS-AS1
20 58831332 intron variant -/A delins 4.5E-02 1
rs398090202
ADCY3 ; LOC105377626
2 24833715 intron variant -/A delins 1
rs550617350
TBX15
1 118939742 intron variant -/A delins 1.6E-04 1
rs35787829
TET1
10 68583439 intron variant -/A delins 7.2E-02 1
rs5831974
AAK1
1.000 0.040 2 69477204 intron variant -/A delins 0.60 1
rs140751051
MNX1
1.000 0.080 7 157000756 intron variant -/A delins 1
rs5833486
PSD4
2 113199603 intron variant -/A delins 0.29 1
rs11451044
COPZ1
12 54322000 intron variant -/A ins 0.68 1
rs36053385
FAM53B
10 124720306 intron variant -/A delins 0.61 1
rs34101942 1.000 0.160 22 39167907 intergenic variant -/A delins 0.68 1
rs147124286
SP1
1.000 0.120 12 53394218 intron variant -/A delins 0.18 1
rs3215853
DOCK8
9 273178 intron variant -/A delins 0.72 1
rs11459029
ARHGEF3
3 56740187 intron variant -/A delins 1
rs139604259
MACO1
1 25442718 intron variant -/A delins 0.58 1
rs11394256
MARCHF8
10 45461799 non coding transcript exon variant -/A delins 0.23 1