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: rs121913293
rs121913293
0.732 0.360 10 87952142 missense variant C/A;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 5 2007 2017
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: rs146650273
rs146650273
0.882 0.160 10 87961042 frameshift variant ACTT/- delins
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 4 1997 2013
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: 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: rs1064793345
rs1064793345
0.752 0.240 10 87961039 missense variant T/C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 2012 2012
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: rs138336847
rs138336847
0.790 0.160 10 87952264 splice region variant G/A;C snv 4.0E-06
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 2008 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: rs863224666
rs863224666
1.000 0.080 10 87933181 missense variant A/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 2 2018 2018
dbSNP: rs1057517809
rs1057517809
0.882 0.160 10 87965286 splice acceptor variant G/A;C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1085308041
rs1085308041
0.763 0.160 10 87965285 splice acceptor variant A/C;G snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1085308043
rs1085308043
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
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: rs1114167621
rs1114167621
0.790 0.160 10 87931045 splice acceptor variant G/A;C;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1114167622
rs1114167622
0.790 0.160 10 87952260 splice donor variant G/C snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1114167650
rs1114167650
0.790 0.160 10 87925562 splice region variant G/A snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1554897854
rs1554897854
0.790 0.160 10 87931042 splice acceptor variant AGTT/- delins
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
dbSNP: rs1554897889
rs1554897889
0.790 0.160 10 87931094 splice region variant G/A;T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017
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: rs1554898242
rs1554898242
0.790 0.160 10 87933252 splice donor variant G/T snv
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.700 1.000 1 2017 2017