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: rs121913291
rs121913291
0.925 0.080 10 87961055 frameshift variant A/-;AA delins
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 2007 2013
dbSNP: rs121913292
rs121913292
1.000 0.080 10 87933148 frameshift variant G/- del
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 2007 2013
dbSNP: rs1060500126
rs1060500126
0.790 0.160 10 87933223 missense variant A/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.800 1.000 3 2004 2015
dbSNP: rs762518389
rs762518389
0.925 0.080 10 87894089 missense variant C/A;G;T snv 4.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.010 1.000 1 2003 2003
dbSNP: rs786201044
rs786201044
0.827 0.200 10 87933165 missense variant T/C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.710 0.857 7 2000 2013
dbSNP: rs121913294
rs121913294
0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 6 2000 2015
dbSNP: rs786201816
rs786201816
1.000 0.080 10 87961100 stop gained C/G;T snv 4.0E-06 7.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 8 1999 2015
dbSNP: rs398123330
rs398123330
1.000 0.080 10 87961048 frameshift variant CTTT/- del
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 4 1999 2014
dbSNP: rs786204928
rs786204928
1.000 0.080 10 87933048 stop gained C/G;T snv 7.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 1999 1999
dbSNP: rs1564566706
rs1564566706
1.000 0.080 10 87957851 splice acceptor variant A/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 5 1998 2017
dbSNP: rs1554897280
rs1554897280
1.000 0.080 10 87925558 splice donor variant G/A;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 1998 2011
dbSNP: rs1564828909
rs1564828909
1.000 0.080 10 87931040 splice acceptor variant TTTTA/- del
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 1998 2011
dbSNP: rs1564828914
rs1564828914
1.000 0.080 10 87931044 splice acceptor variant A/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 1998 2011
dbSNP: rs786204862
rs786204862
1.000 0.080 10 87952117 splice acceptor variant G/A snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 1998 2011
dbSNP: rs1085308048
rs1085308048
0.851 0.320 10 87933175 stop gained T/G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.010 1.000 1 1998 1998
dbSNP: rs1554898053
rs1554898053
1.000 0.080 10 87933018 stop gained C/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 1998 1998
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