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: rs1064651
rs1064651
GBA
13 0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 0.010 1.000 1 2003 2003
dbSNP: rs751377893
rs751377893
F5
65 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs776445885
rs776445885
F2
2 11 46728086 synonymous variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs899127658
rs899127658
F2
82 0.547 0.720 11 46739084 missense variant G/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs991104525
rs991104525
ARSB
4 0.882 0.160 5 78969051 missense variant G/A snv 1.2E-05 7.7E-05 0.010 1.000 1 2013 2013