Gene: FAM222B ×
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: rs28847895
rs28847895
FAM222B
1 17 28845502 intron variant T/C;G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs9892942
rs9892942
FAM222B
4 17 28851743 intron variant C/T snv 0.25 0.700 1.000 1 2016 2016