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: rs1036476
rs1036476
FBN1
1 1.000 0.040 15 48622578 intron variant T/C snv 7.5E-02 0.800 1.000 1 2011 2011