Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs11549029
PROSER3 ; HSPB6
19 35756950 missense variant G/A snv 8.9E-04 1.3E-03 1
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 5
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs41310765
SCN5A
0.882 0.120 3 38575424 missense variant G/A snv 1.4E-04 7.7E-05 5
rs139794067
MYL3
0.925 0.080 3 46860813 missense variant G/A;C;T snv 7.2E-05; 1.7E-04 3
rs1904694
PRKG1
10 51145734 intron variant A/G snv 0.45 1
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1064794243
SCN4A
0.851 0.200 17 63941169 missense variant A/T snv 5
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs376970496
NOX5
15 69028303 missense variant T/C snv 1
rs148398509
HCN4
0.882 0.160 15 73323445 missense variant G/C snv 7.8E-03 7.2E-03 5
rs3211892
CD36
1.000 0.080 7 80661053 intron variant A/G snv 0.97 0.92 2
rs72546668
SSUH2 ; CAV3
0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24