Source: GWASDB

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 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 4
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 4
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 3
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 3