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: rs9929218
rs9929218
0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.850 1.000 6 2008 2016
dbSNP: rs9929218
rs9929218
0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.710 1.000 2 2008 2013
dbSNP: rs9929218
rs9929218
0.732 0.160 16 68787043 intron variant G/A snv 0.28
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2015 2016
dbSNP: rs9939049
rs9939049
0.790 0.080 16 68778398 intron variant A/T snv 0.29
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.710 1.000 2 2019 2020
dbSNP: rs10431923
rs10431923
0.925 0.120 16 68805360 intron variant G/T snv 0.44
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10431923
rs10431923
0.925 0.120 16 68805360 intron variant G/T snv 0.44
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs10431924
rs10431924
0.882 0.120 16 68805399 intron variant T/C snv 0.45
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10431924
rs10431924
0.882 0.120 16 68805399 intron variant T/C snv 0.45
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs10431924
rs10431924
0.882 0.120 16 68805399 intron variant T/C snv 0.45
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11426768
rs11426768
16 68766738 intron variant -/T;TT;TTTTTTTT;TTTTTTTTTTTTTT delins
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs12185157
rs12185157
0.882 0.120 16 68750684 intron variant G/A;C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12185157
rs12185157
0.882 0.120 16 68750684 intron variant G/A;C;T snv
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: rs12185157
rs12185157
0.882 0.120 16 68750684 intron variant G/A;C;T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs12597188
rs12597188
1.000 0.040 16 68780923 intron variant G/A snv 0.33
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs12919719
rs12919719
16 68788438 intron variant C/G snv 0.25
CUI: C0037284
Disease: Skin lesion
Skin lesion
Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs17715799
rs17715799
0.882 0.120 16 68796608 intron variant A/G;T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2018 2018
dbSNP: rs17715799
rs17715799
0.882 0.120 16 68796608 intron variant A/G;T snv
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: rs17715799
rs17715799
0.882 0.120 16 68796608 intron variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs34117943
rs34117943
16 68785740 intron variant T/-;TT;TTT;TTTT delins
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
Malignant melanoma of skin of upper limb
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
Malignant melanoma of skin of lower limb
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs35158985
rs35158985
0.882 0.080 16 68762843 intron variant A/G snv 0.38
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019