Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 3
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 3
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 3
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 2
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 2
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 2
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 1
rs3130968 1.000 0.040 6 31097294 regulatory region variant C/G;T snv 1
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 1
rs6841581
EDNRA
0.882 0.080 4 147480038 upstream gene variant G/A;T snv 1
rs6842241
EDNRA
0.925 0.080 4 147479667 upstream gene variant C/A snv 0.22 1