rs12740374, CELSR2

N. diseases: 8
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 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.810 1.000 1 2011 2018
Low density lipoprotein cholesterol measurement
555 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.800 1.000 5 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
652 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.800 1.000 2 2012 2019
High density lipoprotein measurement
681 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.800 1.000 1 2012 2018
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 5 2008 2012
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3265 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 1 2012 2012