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: rs121917887
rs121917887
10 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 0.080 1.000 8 1995 2018
dbSNP: rs201216664
rs201216664
5 0.851 0.080 17 51171503 missense variant A/G snv 0.020 1.000 2 1995 1999
dbSNP: rs121912438
rs121912438
58 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 0.100 1.000 14 1997 2013
dbSNP: rs74315406
rs74315406
5 0.851 0.160 20 4699870 missense variant A/G snv 0.020 1.000 2 1997 2000
dbSNP: rs1231783932
rs1231783932
APP
11 0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 0.010 1.000 1 1997 1997
dbSNP: rs63750215
rs63750215
19 0.701 0.240 1 226885603 missense variant A/T snv 0.010 1.000 1 1997 1997
dbSNP: rs63750306
rs63750306
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.050 1.000 5 1998 2013
dbSNP: rs63749805
rs63749805
6 0.807 0.120 14 73173577 missense variant C/G;T snv 0.030 1.000 3 1998 2001
dbSNP: rs1211164799
rs1211164799
3 0.882 0.080 17 49973938 missense variant A/T snv 0.010 1.000 1 1998 1998
dbSNP: rs121912443
rs121912443
15 0.732 0.160 21 31663857 missense variant A/G snv 0.030 1.000 3 1999 2007
dbSNP: rs63750646
rs63750646
6 0.807 0.120 14 73217147 missense variant G/C snv 0.010 1.000 1 1999 1999
dbSNP: rs74315407
rs74315407
15 0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 0.010 1.000 1 1999 1999
dbSNP: rs63751163
rs63751163
7 0.807 0.120 14 73192844 missense variant T/C snv 0.020 1.000 2 2000 2001
dbSNP: rs1273925499
rs1273925499
3 0.882 0.080 17 45991557 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs28933385
rs28933385
25 0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs369576054
rs369576054
6 0.807 0.120 4 85994925 missense variant C/T snv 2.8E-05 4.9E-05 0.010 1.000 1 2001 2001
dbSNP: rs377522479
rs377522479
4 0.882 0.080 4 85931021 missense variant C/T snv 2.0E-05 3.5E-05 0.010 < 0.001 1 2001 2001
dbSNP: rs538874513
rs538874513
6 0.807 0.120 1 3730017 missense variant C/G;T snv 8.2E-06; 8.2E-06 0.010 1.000 1 2001 2001
dbSNP: rs63751235
rs63751235
6 0.807 0.120 14 73198117 missense variant C/G snv 0.010 1.000 1 2001 2001
dbSNP: rs749098599
rs749098599
4 0.882 0.080 1 3683085 missense variant C/T snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2001 2001
dbSNP: rs771723690
rs771723690
3 0.882 0.080 4 85570622 synonymous variant G/A snv 1.6E-05 0.010 < 0.001 1 2001 2001
dbSNP: rs786203436
rs786203436
20 0.701 0.280 17 7675125 missense variant A/C;G;T snv 0.010 < 0.001 1 2001 2001
dbSNP: rs121912431
rs121912431
11 0.742 0.160 21 31663829 missense variant G/A;C snv 0.040 1.000 4 2002 2011
dbSNP: rs104893878
rs104893878
21 0.732 0.160 4 89835580 missense variant C/G snv 0.060 1.000 6 2003 2018
dbSNP: rs104893877
rs104893877
59 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 2018