rs35187787, CDH1

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.700 0
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.010 1.000 1 2001 2001
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.010 1.000 1 2001 2001
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.010 1.000 1 2001 2001
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.010 1.000 1 2001 2001
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 0.010 1.000 1 2001 2001