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: rs1990760
rs1990760
IFIH1
33 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 0.700 1.000 1 2010 2010
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2010 2010
dbSNP: rs6498142
rs6498142
CLEC16A
3 16 10987392 intron variant C/G snv 0.77 0.700 1.000 1 2010 2010
dbSNP: rs669408
rs669408 		2 1 232383404 regulatory region variant A/C snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs9271366
rs9271366 		9 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 0.700 1.000 1 2010 2010