Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6503319
MYH3
1.000 0.040 17 10670842 downstream gene variant C/T snv 0.31 1
rs11213630 1.000 0.040 11 110868831 intergenic variant A/G snv 0.55 1
rs1469170 1.000 0.040 11 110870290 intergenic variant A/G snv 0.55 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs3750920
TOLLIP
0.807 0.120 11 1288726 synonymous variant C/T snv 0.40 0.38 1
rs7023548
LOC105376290
1.000 0.040 9 129246489 regulatory region variant C/G;T snv 2.8E-02 1
rs7855466 0.925 0.080 9 133245916 downstream gene variant C/T snv 0.23 3
rs8176751
ABO
1.000 0.040 9 133255635 synonymous variant C/A;T snv 0.13 1
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs8176722
ABO
1.000 0.040 9 133257367 intron variant C/A snv 0.13 0.12 3
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv 3
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 3
rs8176703
ABO
1.000 0.040 9 133260460 intron variant G/T snv 1
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 5
rs8176672
ABO
1.000 0.040 9 133266772 intron variant C/G;T snv 1
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs6755404
ZNF804A
1.000 0.040 2 184932501 intron variant A/C snv 0.82 1
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 2
rs10900585
ATP2B4
1.000 0.040 1 203684896 intron variant G/T snv 0.81 1
rs4951074
ATP2B4
1.000 0.040 1 203691653 intron variant A/G;T snv 2