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: rs63751037
rs63751037
7 0.790 0.080 14 73173642 missense variant A/G snv 0.020 < 0.001 2 1997 2019
dbSNP: rs1179768627
rs1179768627
2 0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 0.010 < 0.001 1 2011 2011
dbSNP: rs1215971988
rs1215971988
1 1.000 0.080 1 226885618 missense variant T/C snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1281129992
rs1281129992
APP
3 0.882 0.080 21 25891730 missense variant C/T snv 4.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1347585131
rs1347585131
APP
1 1.000 0.080 21 26021974 missense variant T/C snv 4.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1396086494
rs1396086494
APP
6 0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1459435816
rs1459435816
APP
1 1.000 0.080 21 26053249 missense variant G/A snv 4.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1482790603
rs1482790603
1 1.000 0.080 1 226891284 missense variant T/C snv 1.2E-05 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs199887707
rs199887707
APP
3 0.882 0.080 21 25911840 missense variant C/T snv 3.8E-04 4.9E-04 0.010 < 0.001 1 2019 2019
dbSNP: rs200487832
rs200487832
APP
1 1.000 0.080 21 25976000 missense variant C/G;T snv 8.0E-06 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs201617677
rs201617677
1 1.000 0.080 14 73173698 missense variant G/A;T snv 6.4E-05 0.010 < 0.001 1 2019 2019
dbSNP: rs202178897
rs202178897
1 1.000 0.080 1 226885596 missense variant G/A;T snv 1.2E-04; 4.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs372642708
rs372642708
APP
2 0.925 0.080 21 26051152 missense variant C/T snv 2.4E-05 9.8E-05 0.010 < 0.001 1 2019 2019
dbSNP: rs557227002
rs557227002
APP
1 1.000 0.080 21 26000158 missense variant G/A snv 2.0E-04 4.9E-05 0.010 < 0.001 1 2019 2019
dbSNP: rs63749806
rs63749806
7 0.827 0.080 14 73186902 missense variant T/C snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63749824
rs63749824
8 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.010 < 0.001 1 2007 2007
dbSNP: rs63750299
rs63750299
2 0.925 0.080 14 73186890 missense variant T/G snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63750522
rs63750522
8 0.827 0.120 14 73173644 missense variant G/A;C snv 0.010 < 0.001 1 2019 2019
dbSNP: rs63750900
rs63750900
9 0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs63750907
rs63750907
6 0.807 0.120 14 73173667 missense variant C/T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs779569800
rs779569800
1 1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 0.010 < 0.001 1 1997 1997
dbSNP: rs63750264
rs63750264
APP
17 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.100 0.909 11 1991 2019
dbSNP: rs63750231
rs63750231
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.100 1.000 14 1996 2019
dbSNP: rs63750526
rs63750526
10 0.776 0.160 14 73192832 missense variant C/A snv 0.100 1.000 10 1997 2019
dbSNP: rs63750306
rs63750306
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.090 1.000 9 1997 2013