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: rs10082479
rs10082479
1 1.000 0.080 10 49621173 intron variant A/T snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs1042173
rs1042173
14 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 0.010 1.000 1 2013 2013
dbSNP: rs1044394
rs1044394
1 1.000 0.080 20 63350733 synonymous variant A/G snv 0.92 0.81 0.010 1.000 1 2011 2011
dbSNP: rs1079597
rs1079597
5 0.827 0.080 11 113425564 intron variant C/T snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs10798059
rs10798059
2 0.925 0.080 1 186830478 intron variant G/A snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs10865246
rs10865246
1 1.000 0.080 2 50443116 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1122530
rs1122530
1 1.000 0.080 9 84849437 intron variant A/G snv 0.22 0.010 1.000 1 2007 2007
dbSNP: rs1131339
rs1131339
2 0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs1137070
rs1137070
9 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 0.010 1.000 1 2019 2019
dbSNP: rs11568817
rs11568817
8 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 0.010 1.000 1 2017 2017
dbSNP: rs1162419578
rs1162419578
APP
2 0.925 0.160 21 25975126 missense variant G/A snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1187272
rs1187272
1 1.000 0.080 9 84789171 intron variant G/A;C snv 0.010 1.000 1 2007 2007
dbSNP: rs12266458
rs12266458
1 1.000 0.080 10 49639951 intron variant C/T snv 0.11 0.010 1.000 1 2010 2010
dbSNP: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.010 1.000 1 2014 2014
dbSNP: rs12466358
rs12466358
1 1.000 0.080 2 232532815 intron variant T/G snv 0.22 0.010 1.000 1 2010 2010
dbSNP: rs12519
rs12519
1 1.000 0.080 9 89013167 3 prime UTR variant T/A;C snv 0.010 1.000 1 2007 2007
dbSNP: rs12718541
rs12718541
2 0.925 0.080 7 50482446 intron variant A/G snv 0.55 0.010 1.000 1 2006 2006
dbSNP: rs12720071
rs12720071
7 0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 0.010 1.000 1 2008 2008
dbSNP: rs130058
rs130058
8 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs1312171358
rs1312171358
1 1.000 0.080 6 88144597 synonymous variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1317286
rs1317286
6 0.925 0.120 15 78603787 intron variant A/G snv 0.30 0.010 1.000 1 2010 2010
dbSNP: rs13273442
rs13273442
4 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 0.010 1.000 1 2014 2014
dbSNP: rs13277254
rs13277254
1 1.000 0.080 8 42694839 upstream gene variant G/A snv 0.66 0.010 1.000 1 2010 2010
dbSNP: rs13280604
rs13280604
7 0.851 0.160 8 42704443 5 prime UTR variant G/A snv 0.62 0.010 1.000 1 2017 2017
dbSNP: rs13286166
rs13286166
1 1.000 0.080 9 741307 intron variant G/A;T snv 0.010 1.000 1 2012 2012