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: rs530514393
rs530514393
FN1
1 1.000 0.080 2 215408367 missense variant T/A;C snv 2.2E-04; 4.0E-06 0.020 1.000 2 1997 2012
dbSNP: rs80101897
rs80101897
FN1
1 1.000 0.080 2 215399334 missense variant T/C snv 4.0E-06 2.1E-05 0.020 1.000 2 1997 2012