Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs11205911
RAB3B
1 51930640 intron variant A/G snv 0.61 1
rs12566236
RAB3B
1 51931271 intron variant G/T snv 0.61 1
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 1
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 1
rs3101457
C1orf100
1 244369912 intron variant G/A snv 0.80 1
rs6698110
RAB3B
1 51938469 intron variant T/C snv 0.60 1
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 1
rs1344674
ZBTB38
3 141406344 intron variant A/G snv 0.55 2
rs6437740
BBX
3 107746970 intron variant T/C snv 0.25 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 1
rs7697556 4 72649596 intergenic variant T/A;C snv 1
rs1013443 5 180774114 intergenic variant A/T snv 1.4E-03 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1