rs3846662, HMGCR

N. diseases: 12
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.
Low density lipoprotein cholesterol measurement
1142 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.800 1.000 4 2009 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.800 1.000 3 2009 2019
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.700 1.000 3 2009 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.700 1.000 1 2011 2011
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.700 1.000 1 2012 2012
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.050 1.000 5 2015 2019
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.020 0.500 2 2019 2019
Familial hypercholesterolemia - heterozygous
34 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2016 2016
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2016 2016
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2016 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2010 2010
Overweight and obesity
CUI: C1561826
Disease: Overweight and obesity
29 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2014 2014