rs1800812, 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.
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 1.000 0.080 4 54228462 intron variant G/C;T snv 0.010 1.000 1 2012 2012
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 1.000 0.080 4 54228462 intron variant G/C;T snv 0.010 1.000 1 2018 2018