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rs28421666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs28421666(A;G)
Make rs28421666(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32624960
is asnp
is mentioned by
dbSNPrs28421666
ebirs28421666
HLIrs28421666
Exacrs28421666
Varsomers28421666
Maprs28421666
PheGenIrs28421666
hapmaprs28421666
1000 genomesrs28421666
hgdprs28421666
ensemblrs28421666
gopubmedrs28421666
geneviewrs28421666
scholarrs28421666
googlers28421666
pharmgkbrs28421666
gwascentralrs28421666
openSNPrs28421666
23andMers28421666
23andMe allrs28421666
SNP Nexus

SNPshotrs28421666
SNPdbers28421666
MSV3drs28421666
GWAS Ctlgrs28421666
GMAF0.08081
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20512145]
Trait Nasopharyngeal carcinoma
Title A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
Risk Allele
P-val 2E-18
Odds Ratio 1.49 [1.37-1.64]
OMIM607107
Desc
Variant
Relatedalso


[PMID 27517745] Nasopharyngeal carcinoma risk prediction via salivary detection of host and Epstein-Barr virus genetic variants.