rs13113
From SNPedia
modifies risk of lymphoma |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs13113(A;A) |
Make rs13113(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 201287439 |
Gene | CASP8 |
is a | snp |
is | mentioned by |
dbSNP | rs13113 |
dbSNP (classic) | rs13113 |
ClinGen | rs13113 |
ebi | rs13113 |
HLI | rs13113 |
Exac | rs13113 |
Gnomad | rs13113 |
Varsome | rs13113 |
LitVar | rs13113 |
Map | rs13113 |
PheGenI | rs13113 |
Biobank | rs13113 |
1000 genomes | rs13113 |
hgdp | rs13113 |
ensembl | rs13113 |
geneview | rs13113 |
scholar | rs13113 |
rs13113 | |
pharmgkb | rs13113 |
gwascentral | rs13113 |
openSNP | rs13113 |
23andMe | rs13113 |
SNPshot | rs13113 |
SNPdbe | rs13113 |
MSV3d | rs13113 |
GWAS Ctlg | rs13113 |
GMAF | 0.3407 |
Max Magnitude | 0 |
[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 18381704] Caspase polymorphisms and genetic susceptibility to multiple myeloma.
[PMID 19318553] 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, |