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: rs63750548
rs63750548
GRN
2 0.925 17 44351035 splice acceptor variant A/G snv 0.700 1.000 10 2006 2017
dbSNP: rs1555611412
rs1555611412
GRN
2 0.925 17 44352339 splice acceptor variant A/G snv 0.700 1.000 5 2006 2012
dbSNP: rs63751296
rs63751296
GRN
2 0.925 17 44351362 splice acceptor variant G/C snv 0.700 1.000 5 2006 2013
dbSNP: rs63750707
rs63750707
GRN
2 0.925 17 44351461 splice donor variant G/A snv 0.700 1.000 3 2006 2012
dbSNP: rs1392550887
rs1392550887
GRN
2 0.925 17 44349241 frameshift variant -/C delins 0.700 0
dbSNP: rs1567887496
rs1567887496
GRN
2 0.925 17 44351607 stop gained C/T snv 0.700 0
dbSNP: rs63749877
rs63749877
GRN
3 0.882 0.120 17 44351139 frameshift variant CACT/- delins 0.700 0
dbSNP: rs770058074
rs770058074
GRN
1 1.000 17 44352365 missense variant C/A;T snv 4.0E-06 0.700 0