Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs969139366
rs969139366
PDGFRA
4 54277974 missense variant T/C snv 3.5E-05
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.020 1.000 2 2017 2017
dbSNP: rs969139366
rs969139366
PDGFRA
4 54277974 missense variant T/C snv 3.5E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression 		0.010 1.000 1 2017 2017
dbSNP: rs969139366
rs969139366
PDGFRA
4 54277974 missense variant T/C snv 3.5E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017