Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555515445
rs1555515445
CDH1
CUI: C4551988
Disease: BLEPHAROCHEILODONTIC SYNDROME 1
BLEPHAROCHEILODONTIC SYNDROME 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs746481984
rs746481984
CDH1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		G 0.720 CausalMutation CLINVAR

dbSNP: rs971882211
rs971882211
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041161
rs886041161
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039685
rs886039685
CDH1
CUI: C4551988
Disease: BLEPHAROCHEILODONTIC SYNDROME 1
BLEPHAROCHEILODONTIC SYNDROME 1 		C 0.700 CausalMutation CLINVAR

dbSNP: rs878854697
rs878854697
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR

dbSNP: rs878854690
rs878854690
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		TG 0.700 CausalMutation CLINVAR

dbSNP: rs876661107
rs876661107
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs876661106
rs876661106
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs876661091
rs876661091
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs876660393
rs876660393
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs876659716
rs876659716
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		A 0.700 CausalMutation CLINVAR

dbSNP: rs876659716
rs876659716
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR

dbSNP: rs876659503
rs876659503
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876659446
rs876659446
CDH1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		C 0.700 CausalMutation CLINVAR

dbSNP: rs876659446
rs876659446
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR

dbSNP: rs876659208
rs876659208
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR

dbSNP: rs876658932
rs876658932
CDH1
CUI: C4551988
Disease: BLEPHAROCHEILODONTIC SYNDROME 1
BLEPHAROCHEILODONTIC SYNDROME 1 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658932
rs876658932
CDH1
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658932
rs876658932
CDH1
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658932
rs876658932
CDH1
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658932
rs876658932
CDH1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658865
rs876658865
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876658575
rs876658575
CDH1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR

dbSNP: rs869312765
rs869312765
CDH1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		T 0.700 CausalMutation CLINVAR