{{Rsnum
|rsid=373496
|Gene=TNFRSF17
|Chromosome=16
|position=11966306
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.03765
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNFRSF17
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 67.1 | 30.1 | 2.7
| ASW | 80.7 | 15.8 | 3.5
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 93.1 | 6.9 | 0.0
| LWK | 77.1 | 22.0 | 0.9
| MEX | 94.8 | 5.2 | 0.0
| MKK | 93.5 | 6.5 | 0.0
| TSI | 99.0 | 0.0 | 1.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=373496
|allele=G
|frequency=0.975
|uid=1103645427717
|type=homozygous_SNP
|hugo=TNFRSF17
|ensembl gene=ENSG00000048462
|ensembl transcript=ENST00000053243
|sift=
|disease=A chromosomal aberration involving TNFRSF17 is found in a form of T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(4;16)(q26;p13) with IL2.
}}

{{PMID Auto
|PMID=16318629
|Title=On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors.
|OA=1
}}

{{PMID Auto
|PMID=18254984
|Title=Screening of functional and positional candidate genes in families with common variable immunodeficiency.
|OA=1
}}

{{GET Evidence
|gene=TNFRSF17
|aa_change=Asn81Ser
|aa_change_short=N81S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs373496
|overall_frequency_n=10321
|overall_frequency_d=10758
|overall_frequency=0.959379
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=107
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

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