Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs10045403
ERAP1
0.882 0.040 5 96812030 upstream gene variant A/G snv 0.23 3
rs34560261
SEMA4B
0.882 0.040 15 90191194 intron variant C/T snv 0.12 3
rs34097647 0.925 6 151108937 intron variant C/T snv 0.16 2
rs6731286 0.925 2 62612684 intron variant A/G;T snv 2
rs8065764 0.925 17 21103149 intergenic variant T/A;C snv 2
rs7749944
HLA-A
0.925 6 29992223 upstream gene variant A/C snv 1.3E-02 2
rs2523616
HLA-B
0.925 6 31352785 intron variant T/C snv 0.84 2
rs112115472
LOC107986770
0.925 7 13606234 intron variant C/T snv 2.0E-02 2
rs147324178
MIR6891 ; HLA-B
0.925 6 31356965 splice region variant T/A;C snv 9.2E-05; 0.85 2
rs111463574
NDUFA12
0.925 12 95005582 upstream gene variant C/T snv 8.1E-02 2
rs760327
ST3GAL1
0.925 8 133490986 intron variant G/C snv 0.59 2
rs62388754
ZNRD1ASP
0.925 6 30033926 intron variant C/T snv 4.9E-02 2