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: rs71579353
rs71579353
VCL ; LOC107984244
1 1.000 0.080 10 74082499 missense variant C/A;T snv 1.1E-04; 8.0E-06 0.700 0
dbSNP: rs863225121
rs863225121
VCL
1 1.000 0.080 10 74094449 missense variant G/T snv 0.700 0