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: rs1002442
rs1002442
ANK3
4 0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs1559473
rs1559473 		4 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs16975050
rs16975050 		4 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 0.700 1.000 1 2014 2014
dbSNP: rs2412208
rs2412208
CAMTA1
5 0.827 0.080 1 7032722 intron variant T/G snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs3852053
rs3852053
MASP1
4 0.851 0.080 3 187219412 3 prime UTR variant T/G snv 0.47 0.700 1.000 1 2014 2014
dbSNP: rs4424056
rs4424056 		4 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 0.700 1.000 1 2014 2014
dbSNP: rs9825420
rs9825420
ITGA9
4 0.851 0.080 3 37562521 intron variant T/G snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs9977018
rs9977018 		4 0.851 0.080 21 41616809 intergenic variant T/G snv 0.24 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: rs4761659
rs4761659
LOC643339
4 0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 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: rs139550538
rs139550538
IDE
5 0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs7117082
rs7117082
OPCML
4 0.851 0.080 11 133522399 intron variant G/T snv 0.22 0.700 1.000 1 2014 2014
dbSNP: rs7830371
rs7830371
CLVS1
4 0.851 0.080 8 61143108 intron variant G/T snv 0.46 0.700 1.000 1 2014 2014
dbSNP: rs748374535
rs748374535
FUS
2 0.925 0.080 16 31185103 missense variant G/T snv 1.3E-05 0.700 0
dbSNP: rs886041389
rs886041389
FUS
2 0.925 0.080 16 31191429 missense variant G/C snv 0.700 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: rs35714695
rs35714695
SARM1
5 0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 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: rs969599
rs969599
PSD3
4 0.851 0.080 8 18567221 intron variant G/A;T snv 0.700 1.000 1 2016 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: rs267606831
rs267606831
FUS
1 1.000 16 31191089 missense variant G/A snv 0.800 1.000 5 2009 2016
dbSNP: rs11061269
rs11061269
ADGRD1
4 0.851 0.080 12 130971904 intron variant G/A snv 7.5E-02 0.700 1.000 1 2014 2014
dbSNP: rs11590421
rs11590421
LOC105378658
4 0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 0.700 1.000 1 2014 2014