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rs1049216

From SNPedia

Orientationminus
Stabilizedminus
Make rs1049216(C;C)
Make rs1049216(C;T)
Make rs1049216(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position184628935
GeneCASP3
is asnp
is mentioned by
dbSNPrs1049216
dbSNP (classic)rs1049216
ClinGenrs1049216
ebirs1049216
HLIrs1049216
Exacrs1049216
Gnomadrs1049216
Varsomers1049216
LitVarrs1049216
Maprs1049216
PheGenIrs1049216
Biobankrs1049216
1000 genomesrs1049216
hgdprs1049216
ensemblrs1049216
geneviewrs1049216
scholarrs1049216
googlers1049216
pharmgkbrs1049216
gwascentralrs1049216
openSNPrs1049216
23andMers1049216
SNPshotrs1049216
SNPdbers1049216
MSV3drs1049216
GWAS Ctlgrs1049216
GMAF0.4036
Max Magnitude0

[PMID 23765963] HuGE systematic review and meta-analysis demonstrate association of CASP-3 and CASP-7 genetic polymorphisms with cancer risk


[PMID 17071630] Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma. rs1049216 is a SNP that has been found to significantly decrease the Non-Hodgkin Lymphoma.


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


[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.


[PMID 18829519OA-icon.png] CASP3 polymorphisms and risk of squamous cell carcinoma of the head and neck.


[PMID 19531679OA-icon.png] Polymorphisms and haplotypes in the caspase-3, caspase-7, and caspase-8 genes and risk for endometrial cancer: a population-based, case-control study in a Chinese population.


[PMID 19938081OA-icon.png] Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.


[PMID 28114230] Association of Casp3 microRNA Target Site (1049216) SNP With the Risk and Progress of Cervical Squamous Cell Carcinoma.


[PMID 28738811OA-icon.png] Associations of genetic variation in CASP3 gene with noise-induced hearing loss in a Chinese population: a case-control study.


[PMID 29930809OA-icon.png] Induction of the apoptotic pathway by oxidative stress in spontaneous preterm birth: Single nucleotide polymorphisms, maternal lifestyle factors and health status.