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: rs121913675
rs121913675
MET
2 0.925 0.080 7 116778953 missense variant C/T snv 0.700 1.000 1 1999 1999
dbSNP: rs121913676
rs121913676
MET
3 0.925 0.080 7 116783421 missense variant G/A;C;T snv 0.700 1.000 1 1999 1999
dbSNP: rs121913677
rs121913677
MET
2 0.925 0.080 7 116783402 missense variant A/G snv 0.700 1.000 1 1999 1999
dbSNP: rs1621
rs1621
MET
2 0.925 0.160 7 116797552 3 prime UTR variant G/A;C snv 0.010 1.000 1 2016 2016