Source: ALL
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: rs876660634
rs876660634
PTEN
10 0.807 0.200 10 87925551 missense variant A/C;G snv 0.700 1.000 8 1998 2015
dbSNP: rs121909223
rs121909223
PTEN
8 0.790 0.160 10 87933129 missense variant T/C;G snv 0.700 1.000 7 1997 2018
dbSNP: rs121909239
rs121909239
PTEN
2 0.925 0.240 10 87957973 missense variant A/G;T snv 0.700 1.000 7 2005 2018
dbSNP: rs121909240
rs121909240
PTEN
2 0.925 0.240 10 87957940 missense variant T/C snv 0.700 1.000 7 2005 2018
dbSNP: rs121913293
rs121913293
PTEN
18 0.732 0.360 10 87952142 missense variant C/A;T snv 0.700 1.000 7 2000 2017
dbSNP: rs786204859
rs786204859
PTEN
3 0.925 0.080 10 87933166 missense variant G/A snv 0.700 1.000 7 1998 2014
dbSNP: rs121909221
rs121909221
PTEN
7 0.790 0.160 10 87952135 missense variant T/A snv 0.700 1.000 6 1997 2011
dbSNP: rs762518389
rs762518389
PTEN
3 0.925 0.080 10 87894089 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 6 2003 2015
dbSNP: rs786201044
rs786201044
PTEN
8 0.827 0.200 10 87933165 missense variant T/C snv 0.700 1.000 6 2000 2014
dbSNP: rs786204858
rs786204858
PTEN
11 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 1.000 5 2013 2018
dbSNP: rs121909225
rs121909225
PTEN
8 0.790 0.160 10 87894049 missense variant T/C;G snv 0.700 1.000 4 1998 2016
dbSNP: rs121909236
rs121909236
PTEN
2 0.925 0.320 10 87925529 missense variant C/G snv 0.700 1.000 4 2001 2016
dbSNP: rs397514560
rs397514560
PTEN
2 0.925 0.240 10 87933151 missense variant C/G;T snv 0.700 1.000 4 2011 2016
dbSNP: rs587782360
rs587782360
PTEN
5 0.851 0.280 10 87933162 missense variant A/G snv 0.700 1.000 4 1999 2013
dbSNP: rs398123321
rs398123321
PTEN
1 1.000 0.080 10 87933090 missense variant T/C snv 0.700 1.000 3 2016 2018
dbSNP: rs786204856
rs786204856
PTEN
4 0.882 0.120 10 87933043 missense variant C/T snv 0.700 1.000 3 2011 2018
dbSNP: rs1057519724
rs1057519724
PTEN
3 1.000 0.080 10 87933236 missense variant G/A;T snv 0.700 1.000 2 2016 2018
dbSNP: rs1064793345
rs1064793345
PTEN
11 0.752 0.240 10 87961039 missense variant T/C snv 0.700 1.000 2 2012 2012
dbSNP: rs1114167623
rs1114167623
PTEN
2 1.000 0.080 10 87933034 missense variant A/C;G snv 0.700 1.000 2 2011 2013
dbSNP: rs121909226
rs121909226
PTEN
7 0.790 0.160 10 87925557 missense variant T/C snv 0.700 1.000 2 2016 2018
dbSNP: rs397514559
rs397514559
PTEN
2 0.925 0.240 10 87952125 missense variant C/A snv 0.700 1.000 2 2012 2016
dbSNP: rs121909222
rs121909222
PTEN
13 0.742 0.240 10 87933127 missense variant A/G snv 0.700 1.000 1 1999 1999
dbSNP: rs121909235
rs121909235
PTEN
8 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs587782343
rs587782343
PTEN
4 0.851 0.200 10 87933073 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1085308040
rs1085308040
PTEN
6 0.851 0.200 10 87961096 missense variant G/A;T snv 0.700 0