{{Rsnum
|rsid=9510787
|Gene=TNFRSF19
|Chromosome=13
|position=23631056
|Orientation=plus
|GMAF=0.1965
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TNFRSF19
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 59.3 | 35.4 | 5.3
| HCB | 51.1 | 47.4 | 1.5
| JPT | 59.3 | 38.9 | 1.8
| YRI | 93.9 | 6.1 | 0.0
| ASW | 80.7 | 17.5 | 1.8
| CHB | 51.1 | 47.4 | 1.5
| CHD | 54.6 | 38.0 | 7.4
| GIH | 72.3 | 26.7 | 1.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 74.1 | 20.7 | 5.2
| MKK | 87.2 | 12.2 | 0.6
| TSI | 49.0 | 44.1 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20512145
|Trait=Nasopharyngeal carcinoma
|Title=A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
|RiskAllele=G
|Pval=2E-9
|OR=1.20
|ORtxt=[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}}

{{omim
|id=607107
|rsnum=9510787
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}