Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs9923231
VKORC1
0.851 0.200 16 31096368 upstream gene variant C/A;G;T snv 6
rs104894021
KCNH2
0.851 0.120 7 150951629 missense variant G/C;T snv 5
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 5
rs121908990
PRKAG2
0.827 0.120 7 151560611 missense variant G/A;C snv 5
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs199472687
KCNQ1
0.827 0.120 11 2527962 missense variant G/A snv 5
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs58912633
LMNA
0.851 0.240 1 156130688 missense variant C/G;T snv 5
rs761740955
FGB
0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 5
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 4
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 4
rs199472708
KCNQ1
0.882 0.080 11 2572015 missense variant G/A snv 4
rs2244613
CES1
0.882 0.120 16 55810697 intron variant G/A;T snv 8.0E-06; 0.73 4
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs72554071
LOC105369689 ; KCNJ8
0.882 0.280 12 21765733 missense variant G/A;C snv 1.8E-03; 4.0E-06 4
rs762624
CDKN1A ; DINOL
0.851 0.280 6 36677811 non coding transcript exon variant A/C;T snv 0.37; 2.4E-05 4
rs121434558
GJA5 ; LOC102723321
0.882 0.120 1 147758977 missense variant G/A snv 3