Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs1403934301
SHBG
0.882 0.120 17 7631317 missense variant G/A snv 3
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs145204276
ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1490867890
MCL1 ; LOC107985203
0.882 0.080 1 150579475 missense variant G/A;C snv 3
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226