Variant ID: 9-107658385-G-A

NM_005502.3(ABCA1):c.67-6909C>T

This variant was identified in 2 publications




Publications:


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: rs2740491
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: rs2740491
PMID: 19060910
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000374733.1 c.-114-6909C>T - intron_variant - 1/4
ENST00000374736.3 c.67-6909C>T - intron_variant - 2/49
ENST00000423487.2 c.67-6909C>T - intron_variant - 2/7
NM_005502.4 c.67-6909C>T - intron_variant - 2/49