Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2183745
LOC105376184
9 101456893 regulatory region variant T/A snv 0.65 1
rs10819937 9 101460951 intergenic variant C/G;T snv 1
rs117047270
SLC26A4
7 107664388 intron variant T/A snv 3.3E-03 1
rs2419607
LOC101927600
10 112218741 upstream gene variant T/G snv 0.43 1
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs11573824
TNFRSF11B
8 118947686 intron variant A/C;T snv 0.67 1
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs74612335
ST3GAL4
11 126368738 intron variant T/C snv 0.15 1
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 1
rs2236653
ST3GAL4
11 126413890 intron variant C/T snv 0.45 1
rs8176720
ABO
9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 2
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs79343853
ABO
9 133270880 intron variant T/C snv 1
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 1
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 4
rs2593704
MGAT5
2 134247706 intron variant G/C snv 0.80 1
rs16856332
ABCB11
2 168984064 intron variant T/A;G snv 1
rs139089160
CDA
1 20592062 intron variant G/A;T snv 1
rs143370804
EIF4G3
1 21024072 intron variant G/A snv 0.34 1
rs2229450
ECE1
1 21247229 synonymous variant G/A;C snv 0.22 1