rs646776, CELSR2

N. diseases: 10
Source: GWASDB ×
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.830 1.000 3 2011 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
94 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.810 1.000 1 2009 2012
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
555 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 6 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
652 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 3 2009 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
681 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 1 2012 2019
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 6 2008 2013
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3265 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
16 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012