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: rs121909668
rs121909668
FUS
8 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.030 1.000 3 2010 2014
dbSNP: rs371030047
rs371030047
FUS
3 0.882 0.080 16 31183971 missense variant C/G snv 0.010 1.000 1 2017 2017
dbSNP: rs886041390
rs886041390
FUS
5 0.827 0.080 16 31191431 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015