Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs763802417
NOX1
0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs72546668
SSUH2 ; CAV3
0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs59270054
LMNA
0.925 0.120 1 156115162 missense variant G/A;C snv 6
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs41310765
SCN5A
0.882 0.120 3 38575424 missense variant G/A snv 1.4E-04 7.7E-05 5
rs397515126
TSC2
16 2084306 frameshift variant -/TCTCCTCG delins 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3853601
DDX39B ; ATP6V1G2-DDX39B
1.000 0.080 6 31531826 intron variant C/G snv 0.13 2
rs376970496
NOX5
15 69028303 missense variant T/C snv 1
rs373721390
LMNA
1 156114996 synonymous variant C/T snv 2.2E-05 2.8E-05 1
rs3211892
CD36
1.000 0.080 7 80661053 intron variant A/G snv 0.97 0.92 2
rs2968857
KCNH2
1.000 0.080 7 150965242 intron variant C/T snv 0.70 2
rs28935490
RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101398432 missense variant C/A;T snv 3.0E-03; 5.4E-06 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50