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: rs752850609
rs752850609
ATP7B
1 1.000 0.160 13 51964894 missense variant C/T snv 4.8E-05 1.4E-05 0.810 1.000 17 1999 2017