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: rs137853235
rs137853235
HGF
1 1.000 0.107 7 81752250 splice region variant C/T snp 4.0E-06 0.700 1 2009 2009