Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013147010
LDLR
1.000 0.080 19 11105492 missense variant C/A snv 1
rs10405652
ZNF561-AS1
1.000 0.080 19 9630447 intron variant G/T snv 0.13 1
rs10411082
ZNF561-AS1
1.000 0.080 19 9630540 intron variant G/A snv 0.31 1
rs10415132
ZNF846
1.000 0.080 19 9752807 intron variant G/A snv 0.37 1
rs10417403
C3P1
1.000 0.080 19 10061840 non coding transcript exon variant T/A;C snv 1
rs10417523
LOC105372270
1.000 0.080 19 9709518 regulatory region variant A/C snv 0.13 1
rs10418705
ZNF562
1.000 0.080 19 9658249 intron variant A/G snv 0.27 1
rs10422772
ZNF561
1.000 0.080 19 9612747 intron variant C/T snv 0.13 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1057516127
LDLR
0.925 0.080 19 11123200 stop gained G/T snv 7.0E-06 4
rs1057516132
LDLR
0.925 0.080 19 11105245 frameshift variant TTTCG/- delins 2
rs1057516134
LDLR
0.925 0.080 19 11120123 frameshift variant A/- delins 2
rs1057516135
LDLR
0.925 0.080 19 11105372 frameshift variant A/- delins 2
rs1057519661
LDLR
0.882 0.080 19 11105587 frameshift variant C/- del 5
rs1057519667
MIR6886 ; LDLR
0.851 0.120 19 11113277 splice acceptor variant G/- delins 4
rs1057519669
MIR6886 ; LDLR
0.925 0.080 19 11113347 missense variant A/G snv 4
rs1057519670
MIR6886 ; LDLR
0.925 0.080 19 11113406 missense variant A/T snv 4
rs1057519673
LDLR ; MIR6886
0.925 0.080 19 11113705 frameshift variant C/- del 4
rs1057519677
LDLR
0.925 0.080 19 11120099 missense variant T/G snv 4
rs1057519682
LDLR
0.925 0.080 19 11120458 frameshift variant -/A delins 2
rs1057519691
PCSK9
0.925 0.080 1 55043958 missense variant T/C;G snv 2
rs1060499841
APOB
1.000 0.080 2 21043911 frameshift variant A/- del 1
rs1060500986
MIR6886 ; LDLR
1.000 0.080 19 11111628 missense variant G/A snv 3
rs1060500987
MIR6886 ; LDLR
1.000 0.080 19 11113360 frameshift variant C/- delins 1
rs1060500988
LDLR
1.000 0.080 19 11120383 frameshift variant T/- del 1