rs1800973, LYZ

N. diseases: 9
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
CUI: C0002726
Disease: Amyloidosis
93 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.020 1.000 2 2005 2006
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
441 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2009 2009
Amyloid nephropathy
CUI: C0268382
Disease: Amyloid nephropathy
7 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.010 1 2003 2003
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2018 2018
Hereditary systemic amyloidosis
CUI: C4081731
Disease: Hereditary systemic amyloidosis
6 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.010 1.000 1 2008 2008
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2016 2016
Oral Ulcer
CUI: C0149745
Disease: Oral Ulcer
101 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2019 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.700 1.000 1 2019 2019