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rs9510787

From SNPedia

Orientationplus
Stabilizedplus
Make rs9510787(A;A)
Make rs9510787(A;G)
Make rs9510787(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position23631056
GeneTNFRSF19
is asnp
is mentioned by
dbSNPrs9510787
ebirs9510787
HLIrs9510787
Exacrs9510787
Varsomers9510787
Maprs9510787
PheGenIrs9510787
hapmaprs9510787
1000 genomesrs9510787
hgdprs9510787
ensemblrs9510787
gopubmedrs9510787
geneviewrs9510787
scholarrs9510787
googlers9510787
pharmgkbrs9510787
gwascentralrs9510787
openSNPrs9510787
23andMers9510787
23andMe allrs9510787
SNP Nexus

SNPshotrs9510787
SNPdbers9510787
MSV3drs9510787
GWAS Ctlgrs9510787
GMAF0.1965
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 G
P-val 2E-9
Odds Ratio 1.20 [1.10-1.30]

The G allele of this SNP in the TNFRSF19 gene is associated with higher odds of nasopharyngeal cancer in people of southern Chinese descent. [PMID 20512145]

OMIM607107
Desc
Variant
Relatedalso


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