Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 8
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 7
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 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
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 6