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: rs28940577
rs28940577
20 0.673 0.607 16 3243410 missense variant T/C snp 0.100 1.000 12 1999 2011
dbSNP: rs61752717
rs61752717
21 0.667 0.607 16 3243407 missense variant T/A,C snp 2.8E-04 1.9E-04 0.100 1.000 12 1999 2011
dbSNP: rs572842823
rs572842823
APP
9 0.821 0.107 21 25897626 missense variant T/A snp 0.070 1.000 7 1998 2013
dbSNP: rs63750306
rs63750306
20 0.692 0.357 14 73173663 missense variant A/C,G,T snp 0.060 1.000 6 1998 2006
dbSNP: rs371425292
rs371425292
APP
8 0.821 0.107 21 25897627 missense variant C/T snp 8.0E-06 0.050 1.000 5 1998 2011
dbSNP: rs11550199
rs11550199
GSN
5 0.846 0.143 9 121312363 missense variant A/G snp 3.2E-03 1.2E-02 0.040 1.000 4 1991 2011
dbSNP: rs63750231
rs63750231
15 0.734 0.179 14 73198100 missense variant A/C,G snp 0.040 1.000 4 2008 2015
dbSNP: rs63750264
rs63750264
APP
19 0.707 0.321 21 25891784 missense variant C/A,G,T snp 0.040 1.000 4 1996 2007
dbSNP: rs63750579
rs63750579
APP
19 0.707 0.214 21 25891856 missense variant C/G,T snp 0.040 1.000 4 1999 2015
dbSNP: rs759304648
rs759304648
GSN
6 0.846 0.107 9 121312479 G/A snp 8.0E-05 0.040 1.000 4 1997 2005
dbSNP: rs781049584
rs781049584
APP
12 0.784 0.214 21 26021917 missense variant T/G snp 8.2E-06 0.040 1.000 4 2011 2015
dbSNP: rs3743930
rs3743930
17 0.715 0.464 16 3254626 missense variant C/G,T snp 7.1E-02 2.6E-02 0.030 0.333 3 2000 2005
dbSNP: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.030 0.667 3 2014 2018
dbSNP: rs63750671
rs63750671
APP
17 0.715 0.179 21 25891858 missense variant G/C snp 0.030 1.000 3 1999 2016
dbSNP: rs63751039
rs63751039
APP
10 0.744 0.179 21 25891855 missense variant T/C snp 0.030 1.000 3 2004 2012
dbSNP: rs74315402
rs74315402
9 0.821 0.179 20 4699570 missense variant C/T snp 0.030 1.000 3 2001 2006
dbSNP: rs75932628
rs75932628
22 0.679 0.250 6 41161514 missense variant C/A,T snp 6.8E-05; 2.6E-03 1.5E-03 0.030 0.667 3 2015 2016
dbSNP: rs759834365
rs759834365
157 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 0.030 0.667 3 2014 2018
dbSNP: rs10524523
rs10524523
7 0.784 0.179 19 44899792 intron variant CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT/C. microsatellite 0.020 0.500 2 2011 2014
dbSNP: rs121909211
rs121909211
12 0.744 0.143 5 136046407 missense variant G/A,T snp 4.0E-05 0.020 1.000 2 2000 2012
dbSNP: rs202074408
rs202074408
APP
8 0.801 0.143 21 26000152 missense variant G/A snp 1.6E-05 0.020 1.000 2 2009 2010
dbSNP: rs34725003
rs34725003
APP
8 0.801 0.143 21 25982424 frameshift variant GG/G in-del 0.020 1.000 2 2009 2010
dbSNP: rs369990738
rs369990738
APP
8 0.801 0.143 21 25975074 missense variant G/A snp 1.2E-05 0.020 1.000 2 2009 2010
dbSNP: rs387906535
rs387906535
LYZ
5 0.821 0.143 12 69350170 missense variant G/C snp 0.020 1.000 2 1999 2000
dbSNP: rs576980684
rs576980684
3 0.878 0.107 10 103458498 missense variant G/A snp 8.1E-06 0.020 1.000 2 2009 2016