Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2664170
GAB3
1.000 0.120 X 154717327 intron variant G/A snv 1
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 3
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 2
rs5753037
HORMAD2 ; LOC105372988
0.925 0.160 22 30185733 intron variant C/A;T snv 2
rs229526
C1QTNF6
1.000 0.120 22 37185382 missense variant G/C;T snv 0.19; 4.0E-06 1
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 2
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs2281808
SIRPG
0.925 0.160 20 1629905 intron variant T/A;C snv 2
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs425105
PRKD2
0.925 0.160 19 46705224 intron variant T/C snv 0.15 2
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs4804000
FKRP
1.000 0.120 19 46773197 intron variant G/A snv 0.16 1
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 1
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs163061
AQP4-AS1
1.000 0.120 18 26893778 intron variant G/C snv 0.68 1
rs727088
CD226
0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 1