Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 5
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs11748327 1.000 0.080 5 4029676 downstream gene variant C/T snv 0.21 2
rs16880442
ITGA1
0.925 0.080 5 52889863 non coding transcript exon variant G/A;T snv 2
rs16964543
ZNF536
1.000 0.080 19 30694303 intron variant T/C snv 0.32 2
rs180803
BCRP1 ; POM121L9P
0.925 0.080 22 24262890 intron variant G/A;T snv 2
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 2
rs2001846 1.000 0.080 8 125466208 upstream gene variant T/A;C snv 2
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33 2
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 2
rs2781668
ARG1 ; MED23
1.000 0.080 6 131576138 intron variant C/T snv 0.16 2
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 2
rs4593108 0.925 0.080 4 147359849 regulatory region variant C/G snv 0.31 2
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv 2
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 2
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 2
rs72689147
GUCY1A1
0.925 0.080 4 155718736 intron variant G/T snv 0.15 2
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 2