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: rs553119528
rs553119528
GRN
3 0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 0.020 1.000 2 2009 2010
dbSNP: rs1026683055
rs1026683055
GRN
3 0.882 0.200 17 44351429 missense variant C/T snv 1.6E-05 1.5E-05 0.010 1.000 1 2016 2016
dbSNP: rs63750541
rs63750541
GRN
4 0.851 0.160 17 44351586 missense variant G/A;C snv 8.4E-04 0.010 1.000 1 2008 2008
dbSNP: rs753070659
rs753070659
GRN
4 0.851 0.160 17 44350481 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs63750869
rs63750869
6 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.020 1.000 2 2007 2011
dbSNP: rs267604921
rs267604921
3 0.925 0.160 17 45993953 missense variant C/A;G;T snv 6.3E-05; 2.5E-04; 5.3E-06 0.010 1.000 1 2016 2016
dbSNP: rs533610448
rs533610448
3 0.882 0.240 17 45983334 missense variant A/T snv 9.8E-05 6.3E-05 0.010 1.000 1 2016 2016
dbSNP: rs63750756
rs63750756
23 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs63751273
rs63751273
42 0.645 0.280 17 46010389 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs762046989
rs762046989
5 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs762104961
rs762104961
3 0.882 0.200 17 46024014 missense variant C/T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1565825132
rs1565825132
2 1.000 0.160 12 64498008 stop gained G/T snv 0.700 0
dbSNP: rs1038579230
rs1038579230
VCP
3 0.882 0.200 9 35067913 missense variant C/A snv 0.010 1.000 1 2016 2016