Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
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
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 4
rs314253
DLG4
17 7188331 downstream gene variant T/C snv 0.37 3
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 3
rs1880889
PDZRN4
12 41327433 intron variant A/C snv 0.91 2
rs2445752
CYP19A1 ; MIR4713HG
15 51284188 intron variant A/G snv 0.30 2
rs6911965
GPLD1
6 24480067 intron variant T/A;C snv 2
rs8176720
ABO
9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 2
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 2
rs10091910
NCOA2
8 70196313 intron variant T/A;C snv 1
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 1
rs10761779
JMJD1C
10 63515167 intron variant A/G snv 0.42 1
rs10819937 9 101460951 intergenic variant C/G;T snv 1
rs10822161
JMJD1C
10 63358443 intron variant G/A;T snv 1
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 1
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1