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: rs63750264
rs63750264
APP
19 0.707 0.321 21 25891784 missense variant C/A,G,T snp 0.060 1.000 6 1997 2012
dbSNP: rs371425292
rs371425292
APP
8 0.821 0.107 21 25897627 missense variant C/T snp 8.0E-06 0.030 1.000 3 2003 2012
dbSNP: rs572842823
rs572842823
APP
9 0.821 0.107 21 25897626 missense variant T/A snp 0.030 1.000 3 2003 2012
dbSNP: rs63750306
rs63750306
20 0.692 0.357 14 73173663 missense variant A/C,G,T snp 0.030 0.667 3 2001 2006
dbSNP: rs63750671
rs63750671
APP
17 0.715 0.179 21 25891858 missense variant G/C snp 0.030 1.000 3 1999 2012
dbSNP: rs781049584
rs781049584
APP
12 0.784 0.214 21 26021917 missense variant T/G snp 8.2E-06 0.030 1.000 3 2002 2014
dbSNP: rs63750215
rs63750215
14 0.734 0.179 1 226885603 missense variant A/T snp 0.020 0.500 2 1997 2001
dbSNP: rs63750311
rs63750311
6 0.846 0.143 14 73192647 missense variant A/C snp 0.020 1.000 2 2000 2003
dbSNP: rs10908821
rs10908821
1 1 161038745 intron variant C/G snp 0.11 0.010 1.000 1 2013 2013
dbSNP: rs17852079
rs17852079
3 1.000 0.071 20 4699899 stop gained C/A,T snp 0.010 1.000 1 2010 2010
dbSNP: rs1799990
rs1799990
19 0.715 0.286 20 4699605 missense variant A/G snp 0.31 0.32 0.010 1.000 1 2013 2013
dbSNP: rs191838178
rs191838178
3 1.000 0.036 22 40407449 missense variant C/T snp 2.4E-05 3.2E-05 0.010 1.000 1 2001 2001
dbSNP: rs2774276
rs2774276
2 1.000 0.036 1 161041926 intron variant G/A,C snp 0.77 0.010 1.000 1 2013 2013
dbSNP: rs2794521
rs2794521
CRP
5 0.878 0.179 1 159715306 intergenic variant C/T snp 0.78 0.010 1.000 1 2012 2012
dbSNP: rs2829887
rs2829887
1 21 25731303 intron variant C/T snp 0.34 0.010 1.000 1 2013 2013
dbSNP: rs3091244
rs3091244
CRP
11 0.784 0.071 1 159714875 intergenic variant G/A,T snp 0.30; 0.13 0.010 1.000 1 2012 2012
dbSNP: rs3093075
rs3093075
7 0.878 0.071 1 159710123 intergenic variant G/T snp 0.13 0.010 1.000 1 2012 2012
dbSNP: rs3764650
rs3764650
6 0.821 0.179 19 1046521 intron variant T/G snp 0.14 0.010 1.000 1 2013 2013
dbSNP: rs398122414
rs398122414
4 0.923 0.071 20 4699898 stop gained C/A snp 0.010 1.000 1 2010 2010
dbSNP: rs63750424
rs63750424
25 0.692 0.214 17 46024061 missense variant C/T snp 1.6E-05 0.010 1.000 1 2001 2001
dbSNP: rs63750522
rs63750522
4 0.878 0.143 14 73173644 missense variant G/A snp 0.010 < 0.001 1 2001 2001
dbSNP: rs63750579
rs63750579
APP
19 0.707 0.214 21 25891856 missense variant C/G,T snp 0.010 < 0.001 1 2010 2010
dbSNP: rs63751273
rs63751273
26 0.692 0.250 17 46010389 missense variant C/T snp 0.010 1.000 1 1999 1999
dbSNP: rs6910730
rs6910730
2 1.000 0.036 6 41278895 intron variant A/G snp 0.21 0.010 1.000 1 2015 2015
dbSNP: rs751861230
rs751861230
APP
7 0.821 0.143 21 26000098 missense variant G/T snp 4.0E-06 0.010 1.000 1 2014 2014