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: rs116107386
rs116107386
AP1S3
1 1.000 2 223777862 missense variant A/C snv 7.6E-03 8.8E-03 0.800 0
dbSNP: rs138292988
rs138292988
AP1S3
2 1.000 2 223777776 missense variant G/A snv 7.6E-03 7.2E-03 0.700 0