Variant ID: 12-117002658-G-A

NM_001085481.3(MAP1LC3B2):c.-102+5420G>A

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: rs2089222
PMID: 20876667
View BVdb publication page



Germline genomic variants associated with childhood acute lymphoblastic leukemia.

Nature Genetics
LR TreviƱo, W Yang, D French, SP Hunger, WL Carroll, M Devidas, C Willman, G Neale, J Downing, SC Raimondi, CH Pui, WE Evans, MV Relling
Publication Date: 2009-09

Variant appearance in text: rs2089222
PMID: 19684603
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000306985.4 c.-102+5420G>A - intron_variant - 1/1
NM_001085481.3 c.-102+5420G>A - intron_variant - 1/1