Gene: FHIT ×
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: rs2365389
rs2365389
FHIT
3 3 61250788 intron variant C/T snv 0.56 0.700 1.000 7 2015 2018
dbSNP: rs1916799
rs1916799
FHIT
3 3 61247301 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1916801
rs1916801
FHIT
1 3 61201372 intron variant A/G;T snv 0.700 1.000 1 2019 2019