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rs398652

From SNPedia

Orientationplus
Stabilizedplus
Make rs398652(A;A)
Make rs398652(A;G)
Make rs398652(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position56058851
is asnp
is mentioned by
dbSNPrs398652
dbSNP (classic)rs398652
ClinGenrs398652
ebirs398652
HLIrs398652
Exacrs398652
Gnomadrs398652
Varsomers398652
LitVarrs398652
Maprs398652
PheGenIrs398652
Biobankrs398652
1000 genomesrs398652
hgdprs398652
ensemblrs398652
geneviewrs398652
scholarrs398652
googlers398652
pharmgkbrs398652
gwascentralrs398652
openSNPrs398652
23andMers398652
SNPshotrs398652
SNPdbers398652
MSV3drs398652
GWAS Ctlgrs398652
GMAF0.3517
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21460395OA-icon.png]
Trait
Title A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer
Risk Allele
P-val 0.000002
Odds Ratio 0.1200 [NR] unit increase


[PMID 23180556] Leukocyte telomere length-related genetic variants in 1p34.2 and 14q21 loci contribute to the risk of esophageal squamous cell carcinoma


[PMID 24844311] 1p34.2 rs621559 and 14q21 rs398652 leukocyte telomere length-related genetic variants contribute to glioma susceptibility