rs7080536, HABP2;NRAP

N. diseases: 27
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.
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2016 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2006 2006