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: rs1391371
rs1391371
HLA-DQA1
2 0.925 0.160 6 32636021 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1444782
rs1444782 		5 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs1888909
rs1888909 		4 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs34210653
rs34210653
ALOX15
8 0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs1178187217
rs1178187217
DNAH11
38 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
dbSNP: rs201943194
rs201943194
DNAH11
38 0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 0.700 0