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rs373496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs373496(C;T)
Make rs373496(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11966306
GeneTNFRSF17
is asnp
is mentioned by
dbSNPrs373496
ebirs373496
HLIrs373496
Exacrs373496
Varsomers373496
Maprs373496
PheGenIrs373496
hapmaprs373496
1000 genomesrs373496
hgdprs373496
ensemblrs373496
gopubmedrs373496
geneviewrs373496
scholarrs373496
googlers373496
pharmgkbrs373496
gwascentralrs373496
openSNPrs373496
23andMers373496
23andMe allrs373496
SNP Nexus

SNPshotrs373496
SNPdbers373496
MSV3drs373496
GWAS Ctlgrs373496
GMAF0.03765
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Venter snp
Source plos
Gene TNFRSF17
allele G
frequency 0.975
sift
HuRef 1103645427717
Disease Association 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 16318629OA-icon.png] 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.


[PMID 18254984OA-icon.png] Screening of functional and positional candidate genes in families with common variable immunodeficiency.


GET Evidence
TNFRSF17-N81S
aa_change Asn81Ser
aa_change_short N81S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.959379
summary