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: rs121913246
rs121913246
MET
7 0.827 0.200 7 116783360 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs121913247
rs121913247
MET
3 0.882 0.200 7 116783359 missense variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs121913671
rs121913671
MET
4 0.882 0.160 7 116783353 missense variant G/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs33917957
rs33917957
MET
10 0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 0.010 1.000 1 2005 2005
dbSNP: rs41281081
rs41281081
MET
3 1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 0.010 1.000 1 2015 2015
dbSNP: rs55985569
rs55985569
MET
3 0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 0.010 1.000 1 2005 2005
dbSNP: rs76322625
rs76322625
MET
3 1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 0.010 1.000 1 2015 2015