Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121908028
LDLR
0.851 0.080 19 11105587 missense variant C/A;G;T snv 8.1E-06; 8.1E-05 6
rs121908030
LDLR
0.851 0.080 19 11107484 missense variant G/A;C;T snv 4.0E-06 6
rs121908031
LDLR
0.851 0.160 19 11120425 stop gained C/A;G snv 8.0E-06 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs137943601
LDLR ; MIR6886
0.851 0.120 19 11113313 missense variant G/A;C snv 8.0E-06 6
rs138947766
LDLR
0.851 0.080 19 11116883 stop gained G/A;C snv 8.0E-06 6
rs139617694
MIR6886 ; LDLR
0.851 0.080 19 11113534 splice acceptor variant G/A;C snv 6
rs144172724
LDLR
0.851 0.080 19 11102774 stop gained G/A;T snv 1.6E-05 6
rs267607213
LDLR
0.851 0.160 19 11100286 stop gained G/A;T snv 6
rs544453230
LDLR
0.882 0.080 19 11110714 missense variant G/A;C snv 2.8E-05; 4.0E-06 6
rs730882094
LDLR
0.827 0.120 19 11110658 missense variant A/C;G snv 1.6E-05 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
rs879255000
LDLR
0.851 0.080 19 11116882 missense variant T/C;G snv 6
rs879255038
LDLR
0.851 0.160 19 11116982 missense variant C/G;T snv 4.0E-06 6
rs879255193
LDLR
0.851 0.120 19 11129512 splice acceptor variant G/A;C snv 6
rs879255196
LDLR
0.827 0.120 19 11129519 missense variant T/G snv 6
rs1057519661
LDLR
0.882 0.080 19 11105587 frameshift variant C/- del 5
rs112029328
LDLR
0.882 0.080 19 11102787 splice donor variant G/A;C;T snv 2.8E-05; 4.0E-06; 4.0E-06; 4.0E-06 5