Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs730882131
rs730882131
1.000 0.080 10 87957999 stop gained C/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs786204855
rs786204855
1.000 0.080 10 87894084 missense variant A/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs786204856
rs786204856
0.882 0.120 10 87933043 missense variant C/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs786204858
rs786204858
0.776 0.280 10 87933079 missense variant A/G;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs786204859
rs786204859
0.925 0.080 10 87933166 missense variant G/A snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs786204863
rs786204863
1.000 0.080 10 87952119 missense variant G/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs863224909
rs863224909
0.732 0.360 10 87960952 stop gained C/A;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312775
rs869312775
0.925 0.120 10 87933103 missense variant A/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312776
rs869312776
1.000 0.080 10 87933167 missense variant T/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312777
rs869312777
0.925 0.120 10 87933245 missense variant C/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312778
rs869312778
1.000 0.080 10 87894063 stop gained G/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312779
rs869312779
1.000 0.080 10 87933183 frameshift variant C/- del
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs869312780
rs869312780
0.925 0.120 10 87957983 frameshift variant AG/- delins
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 0
dbSNP: rs121909232
rs121909232
0.776 0.160 10 87952258 stop gained C/A;G snv 4.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 5 1975 2014
dbSNP: rs587782350
rs587782350
0.776 0.160 10 87957955 missense variant C/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.810 1.000 31 1997 2017
dbSNP: rs121909218
rs121909218
0.672 0.360 10 87933145 missense variant G/A snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.820 1.000 25 1997 2015
dbSNP: rs121909221
rs121909221
0.790 0.160 10 87952135 missense variant T/A snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 23 1997 2015
dbSNP: rs121909223
rs121909223
0.790 0.160 10 87933129 missense variant T/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 23 1997 2015
dbSNP: rs121909225
rs121909225
0.790 0.160 10 87894049 missense variant T/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 23 1997 2015
dbSNP: rs121909226
rs121909226
0.790 0.160 10 87925557 missense variant T/C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 23 1997 2015
dbSNP: rs398123317
rs398123317
0.790 0.160 10 87925550 missense variant T/A;C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 23 1997 2015
dbSNP: rs562015640
rs562015640
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.710 1.000 21 1997 2008
dbSNP: rs121909222
rs121909222
0.742 0.240 10 87933127 missense variant A/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 20 1997 2008
dbSNP: rs121909229
rs121909229
0.683 0.400 10 87933148 missense variant G/A;C;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 20 1997 2008
dbSNP: rs121909230
rs121909230
0.925 0.080 10 87933094 missense variant T/C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 20 1997 2008