Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 6
rs1799943
BRCA2
0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 5
rs41508050
HIF1A-AS3 ; HIF1A
0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4
rs1805120
KCNH2
0.882 0.080 7 150952443 synonymous variant G/A snv 0.30 0.26 3
rs200034939
SCN5A
0.882 0.080 3 38557248 missense variant C/A snv 3.2E-05 3
rs2824292 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 3
rs61688134
ABCC9
0.882 0.080 12 21864476 missense variant C/T snv 7.4E-03 7.5E-03 3
rs974453
SLCO1C1
1.000 0.080 12 20737008 intron variant A/G;T snv 3
rs1049194905
SCN5A
0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs12090554
LOC107985239 ; LINC01350
0.925 0.080 1 185583216 intron variant G/A snv 0.15 2
rs12095080
DIO1
1.000 0.080 1 53911057 3 prime UTR variant A/G snv 0.12 2
rs1237080661
SCN5A
0.925 0.080 3 38604780 stop gained A/G;T snv 2.8E-05 2
rs1353342
PCSK5
0.925 0.080 9 76259853 intron variant A/C snv 0.79 2
rs184934308
SCN5A
0.925 0.080 3 38575342 synonymous variant G/A snv 4.1E-04 9.1E-05 2
rs201698592
KCNQ1 ; KCNQ1-AS1
0.925 0.080 11 2847916 synonymous variant C/T snv 1.7E-04 2.8E-05 2
rs2227721
VTN ; SARM1
0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 2
rs3736235
OLR1
0.925 0.080 12 10160476 non coding transcript exon variant T/C snv 0.43 0.40 2
rs6125
SELP
0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 2
rs740952
KCNH2
0.925 0.080 7 150952515 synonymous variant G/A;T snv 0.30; 7.2E-05 2
rs750678689
SCN5A
0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 2
rs112443954
SIRT5 ; LOC105374937
1.000 0.080 6 13574259 upstream gene variant G/C snv 0.27 1
rs1140713
MIR126 ; EGFL7
1.000 0.080 9 136670833 intron variant C/T snv 0.13 1
rs1175571390
ITGA2
1.000 0.080 5 53056071 missense variant T/C snv 1