Gene: FAM111A ×
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: rs587777011
rs587777011
FAM111A
7 0.925 0.160 11 59153374 missense variant G/A snv 0.800 1.000 3 2013 2014
dbSNP: rs587777012
rs587777012
FAM111A
1 1.000 0.160 11 59153199 missense variant T/C snv 0.800 1.000 3 2013 2014