Variant ID: 11-116621963-T-G

NM_032725.3(BUD13):c.1767-2672A>C

This variant was identified in 4 publications




Publications:


Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study.

Scientific Reports
S Christie, S Robiou-du-Pont, SS Anand, KM Morrison, SD McDonald, G Paré, SA Atkinson, KK Teo, D Meyre
Publication Date: 2017-03-06

Variant appearance in text: rs12292921
PMID: 28250428
View BVdb publication page



Genome-wide association study identifies common variants associated with circulating vitamin E levels.

Human Molecular Genetics
JM Major, K Yu, W Wheeler, H Zhang, MC Cornelis, ME Wright, M Yeager, K Snyder, SJ Weinstein, A Mondul, H Eliassen, M Purdue, A Hazra, CA McCarty, S Hendrickson, J Virtamo, D Hunter, S Chanock, P Kraft, D Albanes
Publication Date: 2011-10-01

Variant appearance in text: rs12292921
PMID: 21729881
View BVdb publication page



Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
OA Panagiotou, E Evangelou, JP Ioannidis
Publication Date: 2010-10-15

Variant appearance in text: rs12292921
PMID: 20876667
View BVdb publication page



Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

Nature Genetics
C Sabatti, SK Service, AL Hartikainen, A Pouta, S Ripatti, J Brodsky, CG Jones, NA Zaitlen, T Varilo, M Kaakinen, U Sovio, A Ruokonen, J Laitinen, E Jakkula, L Coin, C Hoggart, A Collins, H Turunen, S Gabriel, P Elliot, MI McCarthy, MJ Daly, MR Järvelin, NB Freimer, L Peltonen
Publication Date: 2009-01

Variant appearance in text: rs12292921
PMID: 19060910
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000260210.4 c.1767-2672A>C - intron_variant - 9/9
ENST00000375445.3 c.1365-2672A>C - intron_variant - 9/9
ENST00000419189.1 c.*187-2672A>C - intron_variant,NMD_transcript_variant - 3/3
NM_001159736.1 c.1365-2672A>C - intron_variant - 9/9
NM_032725.4 c.1767-2672A>C - intron_variant - 9/9