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: rs751819844
rs751819844
HGF
1 1.000 0.040 7 81705724 missense variant G/A snv 6.4E-05 2.8E-05 0.010 1.000 1 2019 2019