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rs13113

From SNPedia

modifies risk of lymphoma
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs13113(A;A)
Make rs13113(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position201287439
GeneCASP8
is asnp
is mentioned by
dbSNPrs13113
ClinGenrs13113
ebirs13113
HLIrs13113
Exacrs13113
Varsomers13113
Maprs13113
PheGenIrs13113
hapmaprs13113
1000 genomesrs13113
hgdprs13113
ensemblrs13113
gopubmedrs13113
geneviewrs13113
scholarrs13113
googlers13113
pharmgkbrs13113
gwascentralrs13113
openSNPrs13113
23andMers13113
23andMe allrs13113
SNP Nexus

SNPshotrs13113
SNPdbers13113
MSV3drs13113
GWAS Ctlgrs13113
GMAF0.3407
Max Magnitude0

[PMID 17071630] Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma. Rs13113 is a SNP that has been found to significantly decrease the risk of marginal zone lymphoma.


[PMID 18381704OA-icon.png] Caspase polymorphisms and genetic susceptibility to multiple myeloma.


[PMID 19318553OA-icon.png] A breast cancer risk haplotype in the caspase-8 gene.


ClinVar
Risk rs13113(A;A)
Alt rs13113(A;A)
Reference Rs13113(T;T)
Significance Non-pathogenic
Disease Caspase-8 deficiency
Variation info
Gene CASP8
CLNDBN Caspase-8 deficiency
Reversed 0
HGVS NC_000002.11:g.202152162T>A
CLNSRC
CLNACC RCV000407891.1,