Gene: FAM98B ×
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: rs11073328
rs11073328
FAM98B
1 1.000 0.080 15 38472642 intron variant C/T snv 9.3E-02 0.800 1.000 1 2014 2014