PMID: 19336475

Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human molecular genetics
F Drenos, PJ Talmud, JP Casas, L Smeeth, J Palmen, SE Humphries, AD Hingorani
2009-06-15

8 variants were identified in this publication


Variant ID Gene cDNA Protein Consequence Exon Intron
13-113773159-G-T F7 c.1238G>T p.Arg413Leu Missense 9/9 -
6-151252985-G-A MTHFD1L c.1257-4955G>A - IntronicSNV - 11/27
11-116652423-G-A ZPR1 c.1179+451C>T - IntronicSNV - 12/13
11-116652423-G-T ZPR1 c.1179+451C>A - IntronicSNV - 12/13
11-116652423-G-C ZPR1 c.1179+451C>G - IntronicSNV - 12/13
1-55505647-G-A PCSK9 c.137G>A p.Arg46His Missense 1/12 -
13-113773159-G-A F7 c.1238G>A p.Arg413Gln Missense 9/9 -
13-113773159-G-C F7 c.1238G>C p.Arg413Pro Missense 9/9 -