Gene: HGF ×
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: rs5745695
rs5745695
HGF
1 7 81728759 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs984534
rs984534
HGF
1 7 81753374 intron variant C/T snv 0.83 0.700 1.000 1 2018 2018