Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416421760
GATA6 ; GATA6-AS1
1.000 0.080 18 22168362 non coding transcript exon variant C/A snv 1.4E-05 1
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1805017
PLA2G7
0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
rs2227721
VTN ; SARM1
0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 2
rs200478651
F7
1.000 0.080 13 113118414 splice region variant C/A;T snv 8.4E-06; 2.1E-05 1
rs766816990
P2RX5 ; P2RX5-TAX1BP3
1.000 0.080 17 3691667 missense variant C/A;T snv 4.0E-06; 1.2E-05 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 7
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1064039
CST3
0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs28940578
MEFV
0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 16
rs63751001
ABCC6
0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 13
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs41508050
HIF1A-AS3 ; HIF1A
0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4