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: rs121909668
rs121909668
FUS
8 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.800 1.000 13 2009 2016
dbSNP: rs121909669
rs121909669
FUS
2 0.925 0.080 16 31191410 missense variant G/A snv 0.800 1.000 5 2009 2016
dbSNP: rs121909671
rs121909671
FUS
6 0.851 0.120 16 31191419 missense variant G/A;T snv 4.0E-06 0.800 1.000 5 2009 2016
dbSNP: rs1555509693
rs1555509693
FUS
1 1.000 16 31191421 missense variant A/G snv 0.700 1.000 5 2009 2016
dbSNP: rs267606831
rs267606831
FUS
1 1.000 16 31191089 missense variant G/A snv 0.800 1.000 5 2009 2016
dbSNP: rs267606832
rs267606832
FUS
3 0.882 0.040 16 31185061 missense variant C/G;T snv 1.3E-04; 4.1E-06 0.800 1.000 5 2009 2016
dbSNP: rs777819849
rs777819849
FUS
1 1.000 16 31185115 missense variant C/T snv 1.3E-05 0.700 1.000 5 2009 2016
dbSNP: rs886041389
rs886041389
FUS
2 0.925 0.080 16 31191429 missense variant G/C snv 0.700 1.000 5 2009 2016
dbSNP: rs886041390
rs886041390
FUS
5 0.827 0.080 16 31191431 missense variant C/T snv 4.0E-06 0.700 1.000 5 2009 2016
dbSNP: rs10029851
rs10029851 		4 0.851 0.080 4 108706869 intergenic variant A/C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1464443
rs1464443
ERBB4
4 0.851 0.080 2 212050001 intron variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs16938145
rs16938145 		4 0.851 0.080 9 2256092 intergenic variant T/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs17162257
rs17162257 		4 0.851 0.080 1 26602511 upstream gene variant T/A;G snv 0.700 1.000 1 2014 2014
dbSNP: rs3849942
rs3849942
C9orf72 ; LOC107987057
9 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs3849943
rs3849943
C9orf72 ; LOC107987057
5 0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7601234
rs7601234
HOXD10
4 0.851 0.080 2 176116615 5 prime UTR variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs9329300
rs9329300 		4 0.851 0.080 10 2747402 intergenic variant A/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs9568797
rs9568797
OLFM4
4 0.851 0.080 13 53039424 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs969599
rs969599
PSD3
4 0.851 0.080 8 18567221 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs148758737
rs148758737
FUS
2 0.925 0.080 16 31184986 missense variant G/A snv 0.700 0
dbSNP: rs1555509569
rs1555509569
FUS
1 1.000 16 31190961 splice acceptor variant A/- del 0.700 0
dbSNP: rs267606833
rs267606833
FUS
1 1.000 16 31191427 missense variant A/T snv 0.700 0
dbSNP: rs387906627
rs387906627
FUS
2 0.925 0.080 16 31191052 stop gained C/T snv 8.1E-06 0.700 0
dbSNP: rs748374535
rs748374535
FUS
2 0.925 0.080 16 31185103 missense variant G/T snv 1.3E-05 0.700 0
dbSNP: rs387906628
rs387906628
FUS
1 1.000 16 31185031 missense variant G/A snv 6.5E-05 7.0E-06 0.700 0