rs5352, EDNRB;EDNRB-AS1

N. diseases: 5
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.
Hereditary Melanoma
CUI: C1512419
Disease: Hereditary Melanoma
67 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 0.010 1.000 1 2011 2011
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 0.010 1.000 1 1999 1999
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 0.010 1.000 1 2011 2011
melanoma
CUI: C0025202
Disease: melanoma
515 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 0.010 1 2011 2011
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 0.010 1.000 1 2011 2011