Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 8
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7