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: rs4810485
rs4810485
CD40
16 0.732 0.480 20 46119308 intron variant T/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs61735836
rs61735836
FTCD ; FTCD-AS1
3 21 46152973 missense variant C/T snv 5.7E-02 5.6E-02 0.010 1.000 1 2019 2019