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: rs157590
rs157590
3 0.878 0.143 19 44895459 intron variant A/C snp 0.58 0.010 < 0.001 1 2013 2013
dbSNP: rs1768208
rs1768208
4 0.878 0.179 3 39481512 intron variant T/C snp 0.76 0.010 1.000 1 2014 2014
dbSNP: rs2075650
rs2075650
27 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 0.010 1.000 1 2013 2013
dbSNP: rs374191107
rs374191107
FUS
1 1.000 0.107 16 31183984 missense variant C/T snp 1.6E-05 3.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs429358
rs429358
39 0.630 0.321 19 44908684 missense variant T/C snp 0.14 0.16 0.010 1.000 1 2013 2013
dbSNP: rs80356718
rs80356718
7 0.784 0.107 1 11022209 missense variant A/G snp 7.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs8070723
rs8070723
8 0.846 0.214 17 46003698 intron variant A/G snp 0.16 0.010 1.000 1 2014 2014