rs1800458, TTR

N. diseases: 5
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.
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 0.020 0.500 2 2015 2016
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 0.010 1 2016 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 0.010 1.000 1 2007 2007
Senile cardiac amyloidosis
CUI: C0268407
Disease: Senile cardiac amyloidosis
19 0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 0.010 1.000 1 2015 2015
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 0.010 1.000 1 2005 2005