rs121908585, PDGFRA

N. diseases: 9
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 0.827 0.080 4 54285926 missense variant A/T snv 0.800 0.952 21 2003 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.827 0.080 4 54285926 missense variant A/T snv 0.060 0.833 6 2004 2019
Chronic eosinophilic leukemia
CUI: C0346421
Disease: Chronic eosinophilic leukemia
9 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2009 2009
Eosinophilic leukemia
CUI: C0206142
Disease: Eosinophilic leukemia
2 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2009 2009
Hypereosinophilia
CUI: C0745091
Disease: Hypereosinophilia
4 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2014 2014
Metastatic osteosarcoma
CUI: C0278512
Disease: Metastatic osteosarcoma
5 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2019 2019
polyps
CUI: C0032584
Disease: polyps
18 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2014 2014
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2017 2017
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2017 2017