Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8450
DENND4B ; CRTC2
1.000 0.040 1 153947810 3 prime UTR variant G/A snv 0.27 2
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs920435389
FGFR4
1.000 0.040 5 177091064 missense variant G/C snv 3
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs1341991169
LPL
1.000 0.040 8 19939444 missense variant G/A snv 1
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 7
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs2811712
CDKN2B-AS1
0.882 0.080 9 21998036 intron variant G/A snv 0.85 5
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4973768
SLC4A7
0.807 0.120 3 27374522 3 prime UTR variant C/T snv 0.44 7
rs2523608
MIR6891 ; HLA-B
0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 6
rs4713518
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32289560 intron variant A/G;T snv 3
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs2228314
SREBF2
0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs121964971
CBS
0.851 0.160 21 43058215 missense variant G/A snv 1.2E-05 5