Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 4
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 4
rs11953630 5 158418394 intergenic variant C/A;T snv 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs419076
MECOM
3 169383098 intron variant T/A;C snv 3
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 3
rs13082711 3 27496418 intergenic variant T/C snv 0.16 2
rs6544619
LOC112268413
2 42957589 intergenic variant C/T snv 0.52 1
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 3
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 2
rs1918974
MECOM-AS1 ; MECOM
1.000 0.040 3 169448100 intron variant C/T snv 0.57 2
rs2384550 1.000 0.040 12 114914926 regulatory region variant G/A snv 0.33 2
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 1
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
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