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: rs184394424
rs184394424
FREM1
1 1.000 9 14842561 missense variant C/G;T snv 3.4E-04 0.800 1.000 1 2011 2011
dbSNP: rs281875280
rs281875280
FREM1
1 1.000 9 14776147 missense variant T/A;C snv 2.9E-05; 9.7E-06 0.800 1.000 1 2011 2011