rs121908586, PDGFRA

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.
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 1.000 0.080 4 54274869 missense variant T/A;C snv 0.720 1.000 7 2003 2014
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal
2 1.000 0.080 4 54274869 missense variant T/A;C snv 0.700 0
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 1.000 0.080 4 54274869 missense variant T/A;C snv 0.010 1.000 1 2007 2007
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 1.000 0.080 4 54274869 missense variant T/A;C snv 0.010 1 2007 2007
Neuroendocrine Tumors
CUI: C0206754
Disease: Neuroendocrine Tumors
20 1.000 0.080 4 54274869 missense variant T/A;C snv 0.010 1 2007 2007