Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 2
rs10761779
JMJD1C
10 63515167 intron variant A/G snv 0.42 2
rs10819937 9 101460951 intergenic variant C/G;T snv 1
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs12355784
JMJD1C
10 63361805 intron variant C/A;T snv 2
rs16856332
ABCB11
2 168984064 intron variant T/A;G snv 1
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs1780324 1 21495264 intergenic variant A/G snv 0.48 2
rs1883415
GPLD1
0.925 0.040 6 24491247 intron variant A/C snv 0.34 1
rs1976403
NBPF3
1 21439960 upstream gene variant A/C snv 0.33 1
rs2236653
ST3GAL4
11 126413890 intron variant C/T snv 0.45 1
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 2
rs281377
FUT2 ; LOC105447645
0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42 1
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs314253
DLG4
17 7188331 downstream gene variant T/C snv 0.37 3
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 4
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs6984305 8 9320758 intron variant A/T snv 0.85 1
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 3
rs7186908 16 72186474 regulatory region variant G/C snv 0.26 1
rs7267979
ABHD12
20 25317451 intron variant A/G snv 0.58 1