Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 10
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs28942111
PCSK9
0.807 0.120 1 55044016 missense variant T/A snv 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs4363657
SLCO1B1
12 21215788 intron variant T/C snv 0.18 5
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5
rs56225452
SLC27A5 ; LOC105372486 ; ZBTB45
0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs739837
VDR
0.882 0.200 12 47844438 3 prime UTR variant G/C;T snv 5
rs879254535
LDLR
0.925 0.080 19 11105369 missense variant T/A;C;G snv 5
rs258
LPL
8 19954741 intron variant G/A;C;T snv 4
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4