rs545532525, LDLR

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.
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.851 0.200 19 11110753 missense variant G/A snv 0.010 1.000 1 2010 2010
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.851 0.200 19 11110753 missense variant G/A snv 0.010 1.000 1 2010 2010
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.851 0.200 19 11110753 missense variant G/A snv 0.010 1.000 1 2010 2010
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.851 0.200 19 11110753 missense variant G/A snv 0.010 1.000 1 1998 1998
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.200 19 11110753 missense variant G/A snv 0.010 1.000 1 2010 2010