Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
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
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
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 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
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
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 6
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 5