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: rs121913668
rs121913668
MET
4 0.882 0.120 7 116778827 missense variant T/C snv 0.700 1.000 1 1997 1997
dbSNP: rs121913243
rs121913243
MET
7 0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 0.700 0
dbSNP: rs121913246
rs121913246
MET
7 0.827 0.200 7 116783360 missense variant A/G snv 0.700 0
dbSNP: rs121913669
rs121913669
MET
2 0.925 0.120 7 116782027 missense variant G/A;T snv 4.0E-06 0.700 0
dbSNP: rs121913670
rs121913670
MET
3 0.925 0.120 7 116783329 missense variant G/A snv 0.700 0
dbSNP: rs121913671
rs121913671
MET
4 0.882 0.160 7 116783353 missense variant G/A;C snv 0.700 0
dbSNP: rs121913673
rs121913673
MET
3 0.925 0.120 7 116782048 missense variant C/G;T snv 0.700 0
dbSNP: rs786202724
rs786202724
MET
5 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs11762213
rs11762213
MET
2 0.925 0.120 7 116699228 synonymous variant G/A snv 3.3E-02 3.3E-02 0.020 1.000 2 2013 2014