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: rs786205223
rs786205223
IRF7
1 1.000 11 613215 missense variant A/C snv 0.800 0
dbSNP: rs375323253
rs375323253
IRF7
1 1.000 11 613094 stop gained G/A snv 4.0E-06 1.4E-05 0.700 0