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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 5
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
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 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
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G 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
rs11953630 5 158418394 intergenic variant C/A;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
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 3
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 3
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 3
rs419076
MECOM
3 169383098 intron variant T/A;C snv 3
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 3