Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28933979
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.020 1.000 2 2009 2011
dbSNP: rs28939068
rs28939068
CST3
0.790 0.200 20 23635330 missense variant A/T snv
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.020 1.000 2 2002 2004
dbSNP: rs1052006472
rs1052006472
TGFBI
0.827 0.200 5 136060907 missense variant A/G snv
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2003 2003
dbSNP: rs121909211
rs121909211
TGFBI
0.724 0.200 5 136046407 missense variant G/A;T snv 4.0E-05
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2011 2011
dbSNP: rs121913547
rs121913547
LYZ
0.807 0.200 12 69350192 missense variant T/C snv
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2004 2004
dbSNP: rs121918097
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2001 2001
dbSNP: rs1434458385
rs1434458385
TACSTD2
1.000 0.040 1 58576708 missense variant C/A snv 7.0E-06
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2011 2011
dbSNP: rs63750579
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2010 2010
dbSNP: rs74315409
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2003 2003
dbSNP: rs753737986
rs753737986
APP
0.925 0.200 21 26111983 missense variant T/A snv 4.0E-06
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		0.010 1.000 1 2004 2004