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: rs7192
rs7192
HLA-DRA
7 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 0.020 1.000 2 2015 2015
dbSNP: rs9275596
rs9275596 		7 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 0.020 1.000 2 2015 2015
dbSNP: rs1036504
rs1036504
IQCE
2 1.000 0.040 7 2570131 intron variant C/T snv 0.61 0.010 1.000 1 2018 2018
dbSNP: rs2917750
rs2917750
IQCE
2 1.000 0.040 7 2573790 intron variant T/G snv 0.57 0.010 1.000 1 2018 2018
dbSNP: rs4896888
rs4896888
ADGB
2 1.000 0.040 6 146777855 intron variant C/T snv 0.47 0.010 1.000 1 2018 2018