Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759003763
MIR6886 ; LDLR
0.827 0.120 19 11113585 missense variant G/A snv 6
rs879254925
MIR6886 ; LDLR
0.790 0.120 19 11113680 missense variant G/T snv 8
rs1249040838
MIR6886 ; LDLR
0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs33932899
LOC105371082 ; RMI2 ; SOCS1
0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs537765533
IL1RN
0.882 0.080 2 113132839 missense variant G/C snv 2.0E-05 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs12347433
DELEC1 ; TNC
0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs915014
C1orf167 ; MTHFR
0.925 0.040 1 11789412 missense variant T/C snv 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306