rs4970834, CELSR2

N. diseases: 8
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
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 2 2008 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 2 2008 2012
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.700 1.000 1 2009 2009
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.010 1.000 1 2015 2015
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 0.010 1.000 1 2015 2015