Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 1
rs16869786 1.000 0.080 8 102777227 regulatory region variant T/C snv 1.4E-02 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs7674212
SLC9B2
1.000 0.080 4 103067742 intron variant G/A;T snv 1
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs2238367
NPRL3
1.000 0.080 16 105360 intron variant C/T snv 8.1E-03 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 1
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 1
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs6904271
PPIL6
1.000 0.080 6 109395003 intron variant C/G snv 0.15 1
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 4
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs3204953
REV3L ; MFSD4B
0.882 0.160 6 111307423 missense variant C/T snv 0.10 0.10 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs659964
ACAD10
1.000 0.080 12 111692395 intron variant G/A;C snv 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 2
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs11196175
TCF7L2
0.925 0.160 10 112976855 intron variant T/C snv 0.20 1