CDH1, cadherin 1, 999

N. diseases: 508; N. variants: 187
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4783673
rs4783673 		1.000 16 68758190 intron variant T/C;G snv
CUI: C2938924
Disease: Oestrogen receptor positive breast cancer
Oestrogen receptor positive breast cancer 		0.010 1.000 1 2016 2016
dbSNP: rs4783689
rs4783689 		0.925 0.080 16 68819768 intron variant C/T snv 0.30
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2012 2012
dbSNP: rs4783689
rs4783689 		0.925 0.080 16 68819768 intron variant C/T snv 0.30
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs6499199
rs6499199 		1.000 0.080 16 68815934 intron variant C/T snv 0.14
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs71382075
rs71382075 		16 68796765 intron variant A/-;AA;AAA delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7186053
rs7186053 		1.000 0.080 16 68805390 intron variant A/G snv 0.69
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs7196495
rs7196495 		16 68739957 intron variant C/G;T snv
CUI: C0037284
Disease: Skin lesion
Skin lesion 		Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7196661
rs7196661 		16 68740009 intron variant C/T snv 0.80
CUI: C0037284
Disease: Skin lesion
Skin lesion 		Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs7198799
rs7198799 		0.882 0.120 16 68784487 intron variant C/T snv 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs7198799
rs7198799 		0.882 0.120 16 68784487 intron variant C/T snv 0.27
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7198799
rs7198799 		0.882 0.120 16 68784487 intron variant C/T snv 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7200690
rs7200690 		0.925 0.080 16 68744554 intron variant C/T snv 0.23
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7200690
rs7200690 		0.925 0.080 16 68744554 intron variant C/T snv 0.23
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0237123
Disease: Alcohol or Other Drugs use
Alcohol or Other Drugs use 		0.010 1.000 1 2012 2012
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs9929218
rs9929218 		0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015