Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6947830 0.925 0.080 7 15025359 intergenic variant G/A;C snv 2
rs1127065
CAMK2B
1.000 0.040 7 44220272 synonymous variant C/G;T snv 1.7E-02; 0.41 1
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs163182
KCNQ1
0.882 0.160 11 2822986 intron variant G/A;C snv 1
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs3757840
GCK
1.000 0.040 7 44191617 intron variant T/C;G snv 1
rs4846922
GALNT2
1.000 0.040 1 230171436 intron variant T/A;C;G snv 1
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1
rs675
APOA4
1.000 0.040 11 116820959 missense variant T/A;C snv 0.15; 1.2E-03 1
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 1
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 1
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 1
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 4
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2