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: rs377155886
rs377155886
IFNL4
2 1.000 0.080 19 39247213 missense variant T/C snv 1.6E-03 0.010 1.000 1 2018 2018
dbSNP: rs62120527
rs62120527
IFNL3
2 1.000 0.080 19 39243712 missense variant C/T snv 1.3E-02 1.2E-02 0.010 1.000 1 2018 2018