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: rs1925690
rs1925690
7 0.784 0.071 6 87157345 intron variant T/A,C snp 0.92 0.700 1 2012 2012
dbSNP: rs749005
rs749005
7 0.784 0.071 6 6283433 intron variant G/T snp 0.14 0.700 1 2012 2012
dbSNP: rs63750231
rs63750231
15 0.734 0.179 14 73198100 missense variant A/C,G snp 0.080 1.000 8 2004 2015
dbSNP: rs63750526
rs63750526
13 0.744 0.179 14 73192832 missense variant C/A snp 0.080 1.000 8 1997 2014
dbSNP: rs63750306
rs63750306
20 0.692 0.357 14 73173663 missense variant A/C,G,T snp 0.070 1.000 7 1997 2014
dbSNP: rs63749964
rs63749964
APP
7 0.784 0.071 21 25891783 missense variant A/C snp 0.050 1.000 5 1993 2007
dbSNP: rs63750215
rs63750215
14 0.734 0.179 1 226885603 missense variant A/T snp 0.050 1.000 5 1997 2016
dbSNP: rs17125721
rs17125721
9 0.801 0.107 14 73206470 missense variant A/G snp 1.5E-02 1.7E-02 0.040 1.000 4 1999 2013
dbSNP: rs63749884
rs63749884
5 0.846 0.143 1 226888979 missense variant G/A snp 0.040 1.000 4 2000 2012
dbSNP: rs63750264
rs63750264
APP
19 0.707 0.321 21 25891784 missense variant C/A,G,T snp 0.040 1.000 4 1992 2002
dbSNP: rs781049584
rs781049584
APP
12 0.784 0.214 21 26021917 missense variant T/G snp 8.2E-06 0.040 1.000 4 1997 2007
dbSNP: rs371425292
rs371425292
APP
8 0.821 0.107 21 25897627 missense variant C/T snp 8.0E-06 0.030 1.000 3 1998 2004
dbSNP: rs572842823
rs572842823
APP
9 0.821 0.107 21 25897626 missense variant T/A snp 0.030 1.000 3 1998 2004
dbSNP: rs28936379
rs28936379
9 0.821 0.107 1 226888977 missense variant A/C,G,T snp 4.0E-06 3.2E-05 0.020 0.500 2 1999 2006
dbSNP: rs63750001
rs63750001
4 0.846 0.143 14 73219188 missense variant C/T snp 0.020 1.000 2 2010 2015
dbSNP: rs63750083
rs63750083
10 0.744 0.179 14 73219177 missense variant C/A,T snp 0.020 1.000 2 2007 2007
dbSNP: rs63750847
rs63750847
APP
6 0.801 0.143 21 25897620 missense variant C/T snp 4.5E-04 7.6E-04 0.020 1.000 2 2014 2015
dbSNP: rs761592007
rs761592007
4 0.878 0.143 19 44909013 G/A snp 1.5E-05 0.020 1.000 2 2000 2012
dbSNP: rs765670175
rs765670175
7 0.801 0.071 14 73173646 T/A snp 8.0E-06 0.020 1.000 2 2005 2006
dbSNP: rs10524523
rs10524523
7 0.784 0.179 19 44899792 intron variant CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT/C. microsatellite 0.010 1.000 1 2014 2014
dbSNP: rs121917808
rs121917808
4 0.846 0.143 14 73219192 missense variant C/A snp 0.010 1.000 1 2007 2007
dbSNP: rs140501902
rs140501902
6 0.801 0.143 1 226883774 missense variant C/T snp 3.6E-03 4.8E-03 0.010 1.000 1 2006 2006
dbSNP: rs193922916
rs193922916
APP
6 0.821 0.071 21 25897619 missense variant G/A snp 0.010 1.000 1 2011 2011
dbSNP: rs28936380
rs28936380
5 0.821 0.071 1 226885546 missense variant C/G,T snp 1.2E-05 0.010 1.000 1 2005 2005
dbSNP: rs372702043
rs372702043
APP
1 1.000 0.071 21 25976006 missense variant G/A snp 4.0E-06 0.010 1.000 1 2008 2008