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: rs11650788
rs11650788
FAM222B
1 17 28847505 intron variant T/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs7215310
rs7215310
FAM222B
2 17 28761608 intron variant C/A snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs9892942
rs9892942
FAM222B
4 17 28851743 intron variant C/T snv 0.25 0.700 1.000 1 2016 2016