Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs879254925
MIR6886 ; LDLR
0.790 0.120 19 11113680 missense variant G/T snv 8
rs11547917
LDLR
0.807 0.200 19 11107491 stop gained C/A;G;T snv 7
rs193922567
MIR6886 ; LDLR
0.807 0.120 19 11113451 splice donor variant T/A;C snv 7
rs28942111
PCSK9
0.807 0.120 1 55044016 missense variant T/A snv 7
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs879254838
LDLR ; MIR6886
0.827 0.120 19 11113314 missense variant A/C;T snv 7
rs879254965
LDLR
0.827 0.200 19 11116140 missense variant G/A;C;T snv 7
rs879255051
LDLR
0.827 0.120 19 11120091 splice acceptor variant G/A;C snv 7
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs139617694
MIR6886 ; LDLR
0.851 0.080 19 11113534 splice acceptor variant G/A;C snv 6
rs267607213
LDLR
0.851 0.160 19 11100286 stop gained G/A;T snv 6
rs759003763
MIR6886 ; LDLR
0.827 0.120 19 11113585 missense variant G/A snv 6
rs879254592
LDLR
0.827 0.120 19 11105517 missense variant G/A;C;T snv 6
rs879254642
LDLR
0.882 0.120 19 11105589 missense variant A/C;G snv 6
rs879254712
LDLR
0.827 0.200 19 11107470 frameshift variant C/- del 6
rs879254851
LDLR ; MIR6886
0.882 0.120 19 11113368 missense variant T/C snv 6
rs879254977
LDLR
0.827 0.120 19 11116168 stop gained -/GCTGGTGA delins 6