Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs869312687
RIT1
0.925 0.080 1 155910695 missense variant T/G snv 8
rs121908596
MAP2K1
0.807 0.240 15 66436837 missense variant G/A;T snv 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs1060501439
MYH7
0.925 0.080 14 23424938 missense variant T/A snv 4
rs1436109
NCAM1
1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 3
rs4966014
IGF1R
0.882 0.200 15 98704789 intron variant C/G;T snv 3
rs755492182
ACTN2
0.882 0.080 1 236735677 missense variant C/T snv 3
rs1050606
ANXA5
1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs1277204441
ACE
0.925 0.080 17 63479775 missense variant C/T snv 7.0E-06 2
rs1349963459
PSEN1
0.925 0.080 14 73170901 missense variant G/T snv 2
rs17132261
TMEM232
1.000 0.080 5 110672513 intron variant C/T snv 4.8E-02 2
rs2292462
NMB
1.000 0.080 15 84657523 intron variant G/C;T snv 2
rs10500279
RYR1
1.000 0.080 19 38544428 intron variant G/C snv 5.6E-02 1
rs17168525
MTPN ; LUZP6
1.000 0.080 7 135928514 3 prime UTR variant G/A snv 1.4E-02 1
rs1957757
HIF1A-AS3 ; HIF1A
1.000 0.080 14 61730230 intron variant T/C snv 0.74 1
rs1974201
ENPP1
1.000 0.080 6 131889981 intron variant G/A;C;T snv 1
rs2071090
RYR1
1.000 0.080 19 38524814 intron variant T/C snv 0.15 1
rs2960321
RYR1
1.000 0.080 19 38557523 intron variant C/A snv 0.18 1