rs756091827, MYC;CASC11

N. diseases: 6
Source: CLINVAR ×
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.
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
211 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
153 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
102 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
33 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
98 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2014 2014
NEUROBLASTOMA, SUSCEPTIBILITY TO
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
34 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2016 2016