Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10045403
rs10045403
ERAP1
3 0.882 0.040 5 96812030 upstream gene variant A/G snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs111463574
rs111463574
NDUFA12
2 0.925 12 95005582 upstream gene variant C/T snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs112115472
rs112115472
LOC107986770
2 0.925 7 13606234 intron variant C/T snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs147324178
rs147324178
HLA-B ; MIR6891
2 0.925 6 31356965 splice region variant T/A;C snv 9.2E-05; 0.85 0.700 1.000 1 2019 2019
dbSNP: rs1800440
rs1800440
CYP1B1
29 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs2523616
rs2523616
HLA-B
2 0.925 6 31352785 intron variant T/C snv 0.84 0.700 1.000 1 2019 2019
dbSNP: rs34097647
rs34097647 		2 0.925 6 151108937 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs34560261
rs34560261
SEMA4B
3 0.882 0.040 15 90191194 intron variant C/T snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs62388754
rs62388754
ZNRD1ASP
2 0.925 6 30033926 intron variant C/T snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs6731286
rs6731286 		2 0.925 2 62612684 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs760327
rs760327
ST3GAL1
2 0.925 8 133490986 intron variant G/C snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs7749944
rs7749944
HLA-A
2 0.925 6 29992223 upstream gene variant A/C snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs8065764
rs8065764 		2 0.925 17 21103149 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6471
rs6471
CYP21A2
24 0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 0.010 1.000 1 2019 2019