rs6657811, CELSR2

N. diseases: 4
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 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 0.800 1.000 4 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 0.800 1.000 3 2012 2019
High density lipoprotein measurement
1440 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 0.700 1.000 2 2015 2018
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 0.700 1.000 2 2008 2012