Gene: FCHO2 ×
Source: INFERRED ×
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: rs26578
rs26578
FCHO2
2 5 73004636 intron variant T/A snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs75599919
rs75599919
FCHO2
2 5 73011938 intron variant G/T snv 7.5E-02 0.700 1.000 1 2019 2019