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: rs34637584
rs34637584
47 0.630 0.321 12 40340400 missense variant G/A snp 5.3E-04 1.9E-04 0.020 0.500 2 2010 2016
dbSNP: rs371425292
rs371425292
APP
8 0.821 0.107 21 25897627 missense variant C/T snp 8.0E-06 0.020 1.000 2 2005 2012
dbSNP: rs572842823
rs572842823
APP
9 0.821 0.107 21 25897626 missense variant T/A snp 0.020 1.000 2 2005 2012
dbSNP: rs1018381
rs1018381
5 0.923 0.036 6 15656839 intron variant G/A snp 0.14 0.010 1.000 1 2009 2009
dbSNP: rs104893877
rs104893877
31 0.679 0.250 4 89828149 missense variant C/T snp 0.010 1.000 1 2016 2016
dbSNP: rs121912438
rs121912438
47 0.630 0.464 21 31667299 missense variant G/A,C snp 1.2E-05; 8.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs1329650
rs1329650
5 0.878 0.071 10 91588363 regulatory region variant G/A,T snp 1.6E-04; 0.28 0.010 1.000 1 2013 2013
dbSNP: rs1344706
rs1344706
13 0.769 0.071 2 184913701 intron variant A/C,T snp 0.31 0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
58 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2017 2017
dbSNP: rs202074408
rs202074408
APP
8 0.801 0.143 21 26000152 missense variant G/A snp 1.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs2189814
rs2189814
3 0.923 0.036 7 86702440 intron variant T/A,C snp 0.25 0.010 1.000 1 2011 2011
dbSNP: rs2344484
rs2344484
3 0.923 0.036 5 135540941 intergenic variant A/G snp 0.45 0.010 1.000 1 2009 2009
dbSNP: rs28936379
rs28936379
9 0.821 0.107 1 226888977 missense variant A/C,G,T snp 4.0E-06 3.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs33939927
rs33939927
18 0.734 0.107 12 40310434 missense variant C/A,G,T snp 4.0E-06; 1.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs34725003
rs34725003
APP
8 0.801 0.143 21 25982424 frameshift variant GG/G in-del 0.010 1.000 1 2016 2016
dbSNP: rs369990738
rs369990738
APP
8 0.801 0.143 21 25975074 missense variant G/A snp 1.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs387906709
rs387906709
6 0.821 0.107 X 56565363 missense variant C/A,T snp 0.010 1.000 1 2015 2015
dbSNP: rs4673
rs4673
21 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2012 2012
dbSNP: rs53576
rs53576
23 0.692 0.107 3 8762685 intron variant A/G,T snp 0.67 0.010 < 0.001 1 2010 2010
dbSNP: rs5522
rs5522
15 0.734 0.286 4 148436323 missense variant C/T snp 0.88 0.89 0.010 1.000 1 2013 2013
dbSNP: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.010 1.000 1 2016 2016
dbSNP: rs6295
rs6295
32 0.667 0.179 5 63962738 intron variant C/G snp 0.49 0.010 1.000 1 2015 2015
dbSNP: rs63750306
rs63750306
20 0.692 0.357 14 73173663 missense variant A/C,G,T snp 0.010 1.000 1 2005 2005
dbSNP: rs63750424
rs63750424
25 0.692 0.214 17 46024061 missense variant C/T snp 1.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs63750756
rs63750756
18 0.734 0.107 17 46010324 missense variant T/G snp 2.6E-05 0.010 1.000 1 2005 2005