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rs6774494

From SNPedia

Orientationplus
Stabilizedplus
Make rs6774494(A;A)
Make rs6774494(A;G)
Make rs6774494(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position169364845
GeneMECOM
is asnp
is mentioned by
dbSNPrs6774494
ebirs6774494
HLIrs6774494
Exacrs6774494
Varsomers6774494
Maprs6774494
PheGenIrs6774494
hapmaprs6774494
1000 genomesrs6774494
hgdprs6774494
ensemblrs6774494
gopubmedrs6774494
geneviewrs6774494
scholarrs6774494
googlers6774494
pharmgkbrs6774494
gwascentralrs6774494
openSNPrs6774494
23andMers6774494
23andMe allrs6774494
SNP Nexus

SNPshotrs6774494
SNPdbers6774494
MSV3drs6774494
GWAS Ctlgrs6774494
GMAF0.4862
Max Magnitude
? (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 1E-8
Odds Ratio 1.19 [1.12-1.27]
OMIM607107
Desc
Variant
Relatedalso


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