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: rs768678989
rs768678989
MET
1 1.000 0.080 7 116771932 missense variant C/T snv 2.8E-05 0.700 0
dbSNP: rs771333219
rs771333219
MET
1 1.000 0.080 7 116759444 missense variant C/T snv 1.2E-04 8.4E-05 0.700 0
dbSNP: rs40239
rs40239
MET
4 0.851 0.120 7 116677823 intron variant G/A snv 0.87 0.010 1.000 1 2014 2014