Source: ALL
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: rs121918403
rs121918403
ENO3
1 1.000 0.080 17 4955097 missense variant G/A;C;T snv 2.0E-04; 4.0E-06; 1.2E-05 0.800 1.000 1 2001 2001
dbSNP: rs121918404
rs121918404
ENO3
1 1.000 0.080 17 4956626 missense variant G/A snv 1.7E-04 1.2E-04 0.700 1.000 1 2001 2001