Source: CLINVAR

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: rs36053993
rs36053993
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 34 2002 2016
dbSNP: rs34612342
rs34612342
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 23 2002 2017
dbSNP: rs140342925
rs140342925
0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 12 2002 2017
dbSNP: rs374950566
rs374950566
1.000 0.120 1 45332215 missense variant G/A snv 1.2E-05 1.4E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 11 2002 2016
dbSNP: rs529008617
rs529008617
0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 11 2002 2017
dbSNP: rs34126013
rs34126013
0.925 0.160 1 45332458 missense variant G/A snv 6.8E-05 2.1E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 9 2002 2016
dbSNP: rs587782228
rs587782228
0.882 0.120 1 45330557 missense variant C/A;T snv 4.2E-06; 4.2E-06
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 9 2002 2017
dbSNP: rs747993448
rs747993448
1.000 0.120 1 45332795 missense variant G/A snv 4.0E-06 2.8E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 9 2004 2017
dbSNP: rs769237459
rs769237459
1.000 0.120 1 45332279 missense variant G/A snv 8.0E-06
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 8 2002 2017
dbSNP: rs143353451
rs143353451
0.851 0.120 1 45332794 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 7 2004 2017
dbSNP: rs34612342
rs34612342
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
0.800 1.000 5 2005 2019
dbSNP: rs36053993
rs36053993
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 0.941 5 2002 2019
dbSNP: rs34612342
rs34612342
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 4 2002 2019
dbSNP: rs730881833
rs730881833
0.827 0.160 1 45332242 missense variant C/A;T snv 4.0E-06; 2.8E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 4 2007 2015
dbSNP: rs876659676
rs876659676
1.000 0.120 1 45332252 missense variant T/C snv 4.0E-06 1.4E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 4 2002 2016
dbSNP: rs1057517765
rs1057517765
1.000 0.120 1 45332466 missense variant T/C;G snv
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 1.000 3 2008 2009
dbSNP: rs1060501335
rs1060501335
0.925 0.120 1 45331684 missense variant A/G snv
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.800 0
dbSNP: rs371848318
rs371848318
1.000 0.040 1 45341543 missense variant G/A snv 8.0E-06
Congenital pontocerebellar hypoplasia type 7
0.800 1.000 0 2017 2017
dbSNP: rs36053993
rs36053993
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
0.770 1.000 7 2005 2017
dbSNP: rs140342925
rs140342925
0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
0.710 1.000 4 2005 2015
dbSNP: rs587780078
rs587780078
0.882 0.120 1 45331514 frameshift variant -/CC delins 1.6E-04 2.7E-04
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
0.710 1.000 4 2009 2020
dbSNP: rs34612342
rs34612342
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.710 1.000 0 2015 2015
dbSNP: rs36053993
rs36053993
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 1.000 23 2002 2014
dbSNP: rs587778541
rs587778541
0.925 0.120 1 45331219 inframe deletion CCT/- delins 9.5E-05 2.8E-05
Colorectal Adenomatous Polyposis, Autosomal Recessive
0.700 1.000 20 2003 2015
dbSNP: rs529008617
rs529008617
0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 18 2005 2017