Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs367899983
BNC2
1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 1
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 1
rs12379183
BNC2
1.000 0.120 9 16865701 intron variant A/G snv 0.26 1
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs12938171
INTS2
1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 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
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 1
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 1
rs4445329 1.000 0.120 9 16911759 intergenic variant G/A;C snv 1
rs4961501
BNC2
1.000 0.120 9 16851680 intron variant T/A;C;G snv 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 1
rs7861573
BNC2
1.000 0.120 9 16862282 intron variant A/G;T snv 1
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 1
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 2
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 2
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 2
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 1