rs12445050, PLCG2

N. diseases: 3
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 16 81837364 intron variant C/T snv 9.6E-02 0.700 1.000 2 2019 2019
Platelet Component Distribution Width Measurement
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
200 16 81837364 intron variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
371 16 81837364 intron variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016