Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs397516089
MYH7
0.827 0.080 14 23429807 missense variant C/G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs587782951
JPH2
0.807 0.080 20 44160305 missense variant G/T snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs73956431
B4GALT6
0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1559279177
HJV
0.851 0.160 1 146018661 frameshift variant G/- del 5
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs740363
HSPA12A
0.851 0.080 10 116816095 intron variant G/A snv 0.40 5
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs13058338
RAC2
1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/C snv 4