Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs1339552
BNC2
1.000 0.120 9 16848792 intron variant C/T snv 0.52 1
rs1416742
BNC2
1.000 0.120 9 16856885 intron variant G/A snv 0.43 1
rs4961501
BNC2
1.000 0.120 9 16851680 intron variant T/A;C;G snv 1
rs7861573
BNC2
1.000 0.120 9 16862282 intron variant A/G;T snv 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 1
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 1
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 1
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 1
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 1
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 1
rs12938171
INTS2
1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 1
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 1
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 1
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 1
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 1
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 1
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 1