Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6