rs1440200916, PDGFRA

N. diseases: 2
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 4 54258803 missense variant G/C;T snv 0.010 1.000 1 2012 2012
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
55 4 54258803 missense variant G/C;T snv 0.010 1.000 1 2015 2015