Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145905715
RIC3 ; TUB
11 8100687 intron variant -/AT delins 3.5E-04 1
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 3
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs34515106
PLEK
2 68380846 missense variant A/C snv 6.7E-03 1.9E-03 2
rs11597086
CHUK
10 100193948 non coding transcript exon variant A/C snv 0.30 0.29 1
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 1
rs2737229
TRPS1
8 115636338 intron variant A/C snv 0.48 1
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 1
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1
rs6987225
MATN2
8 97963444 intron variant A/C snv 8.7E-02 1
rs7849420
MIR31HG
9 21499625 intron variant A/C snv 0.65 1
rs8026235
ACAN
15 88806225 intron variant A/C snv 1.7E-02 1
rs9332492
F5
1 169583872 intron variant A/C snv 4.8E-02 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs12113155
PRKAG2
7 151607887 intron variant A/C;G snv 3
rs13465
ILF3
19 10692116 3 prime UTR variant A/C;G snv 3
rs598962
ABCD3
1 94451093 intron variant A/C;G snv 3
rs655246 1 109289661 downstream gene variant A/C;G snv 3
rs7162932
TPM1
15 63060452 intron variant A/C;G snv 3
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 2
rs1168046
DOCK7
1 62518022 intron variant A/C;G snv 2
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2