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.
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
288 0.821 0.143 2 29220829 missense variant G/C,T snp 0.800 1.000 17 2008 2016
NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
CUI: C2751681
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
13 0.821 0.143 2 29220829 missense variant G/C,T snp 0.800 3 2008 2011
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.821 0.143 2 29220829 missense variant G/C,T snp 0.700 2 2012 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.821 0.143 2 29220829 missense variant G/C,T snp 0.700 1 2011 2011
Benign Soft Tissue Tumor of Uncertain Differentiation
1 0.821 0.143 2 29220829 missense variant G/C,T snp 0.700 1 2011 2011
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
87 0.821 0.143 2 29220829 missense variant G/C,T snp 0.100 1.000 13 2008 2016
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
16 0.821 0.143 2 29220829 missense variant G/C,T snp 0.010 1.000 1 2012 2012
Inflammatory Myofibroblastic Tumor
CUI: C0334121
Disease: Inflammatory Myofibroblastic Tumor
3 0.821 0.143 2 29220829 missense variant G/C,T snp 0.010 1.000 1 2011 2011
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.821 0.143 2 29220829 missense variant G/C,T snp 0.010 1.000 1 2015 2015