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: rs387906789
rs387906789
VCP
14 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.800 1.000 13 2005 2018
dbSNP: rs121909334
rs121909334
VCP
10 0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 0.800 1.000 11 2004 2016
dbSNP: rs121909329
rs121909329
VCP
11 0.763 0.200 9 35065363 missense variant C/A;G;T snv 0.800 1.000 6 2004 2015
dbSNP: rs121909335
rs121909335
VCP
9 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.700 1.000 9 2005 2016
dbSNP: rs121909330
rs121909330
VCP
11 0.752 0.200 9 35065364 missense variant G/A;C;T snv 0.700 1.000 8 2004 2017
dbSNP: rs1554669087
rs1554669087
VCP
2 0.925 0.200 9 35067916 missense variant G/A snv 0.700 1.000 7 2006 2016
dbSNP: rs387906790
rs387906790
VCP
2 0.925 9 35059723 missense variant C/G;T snv 4.0E-06 0.700 1.000 2 2010 2013