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rs4324798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs4324798(A;A)
Make rs4324798(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position28808340
GeneTRNAF5
is asnp
is mentioned by
dbSNPrs4324798
ebirs4324798
HLIrs4324798
Exacrs4324798
Varsomers4324798
Maprs4324798
PheGenIrs4324798
hapmaprs4324798
1000 genomesrs4324798
hgdprs4324798
ensemblrs4324798
gopubmedrs4324798
geneviewrs4324798
scholarrs4324798
googlers4324798
pharmgkbrs4324798
gwascentralrs4324798
openSNPrs4324798
23andMers4324798
23andMe allrs4324798
SNP Nexus

SNPshotrs4324798
SNPdbers4324798
MSV3drs4324798
GWAS Ctlgrs4324798
GMAF0.05096
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19465454] The TERT-CLPTM1L lung cancer susceptibility variant associates with higher DNA adduct formation in the lung

GWAS snp
PMID [PMID 19836008OA-icon.png]
Trait Lung adenocarcinoma
Title A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma
Risk Allele A
P-val 2E-8
Odds Ratio 1.16 [1.09-1.24]

[PMID 20056643OA-icon.png] A rigorous and comprehensive validation: common genetic variations and lung cancer


[PMID 21750227] Single-nucleotide polymorphisms (5p15.33, 15q25.1, 6p22.1, 6q27 and 7p15.3) and lung cancer survival in the European Prospective Investigation into Cancer and Nutrition (EPIC)

[PMID 20548021OA-icon.png] Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.


GET Evidence
rs4324798
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0703125
summary