Variant ID: 3-37518545-T-A

NM_002207.2(ITGA9):c.420+3594T>A

This variant was identified in 4 publications




Publications:


Genome-Wide Association Studies of Cancer in Diverse Populations.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
SL Park, I Cheng, CA Haiman
Publication Date: 2018-04

Variant appearance in text: rs189897
PMID: 28637795
View BVdb publication page



A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
JX Bei, WH Su, CC Ng, K Yu, YM Chin, PJ Lou, WL Hsu, JD McKay, CJ Chen, YS Chang, LZ Chen, MY Chen, Q Cui, FT Feng, QS Feng, YM Guo, WH Jia, AS Khoo, WS Liu, HY Mo, KC Pua, SH Teo, KP Tse, YF Xia, H Zhang, GQ Zhou, JJ Liu, YX Zeng, A Hildesheim,
Publication Date: 2016-01

Variant appearance in text: rs189897
PMID: 26545403
View BVdb publication page



Genetic predisposition factors and nasopharyngeal carcinoma risk: a review of epidemiological association studies, 2000-2011: Rosetta Stone for NPC: genetics, viral infection, and other environmental factors.

Seminars In Cancer Biology
A Hildesheim, CP Wang
Publication Date: 2012-04

Variant appearance in text: rs189897
PMID: 22300735
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: rs189897
PMID: 20876667
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000264741.5 c.420+3594T>A - intron_variant - 3/27
ENST00000422441.1 c.420+3594T>A - intron_variant - 3/15
NM_002207.3 c.420+3594T>A - intron_variant - 3/27