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: rs17549193
rs17549193
FCN2
1 1.000 0.040 9 134887180 missense variant C/T snv 0.26 0.30 0.010 1.000 1 2015 2015