Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1025423410
TLR1
4 38798831 start lost T/C snv 1
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs10521145
SGF29
16 28585563 intron variant G/A snv 0.11 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs11122576
AGT
1.000 0.080 1 230710933 intron variant T/C snv 8.2E-02 2
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11568054
AGT
1 230709809 intron variant G/A snv 3.6E-02 1
rs11643718
SLC12A3
0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs1191455921
LMX1B
0.925 0.240 9 126693319 missense variant G/A snv 3
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs121912863
COL4A4
1.000 2 227008112 missense variant G/A snv 1.6E-04 1.8E-04 2
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs121918673
HNF1B
0.925 0.200 17 37701122 missense variant G/C snv 1.9E-05 3
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100