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rs1049253

From SNPedia

Orientationminus
Stabilizedplus
Make rs1049253(C;C)
Make rs1049253(C;T)
Make rs1049253(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position184627797
GeneCASP3
is asnp
is mentioned by
dbSNPrs1049253
ebirs1049253
HLIrs1049253
Exacrs1049253
Varsomers1049253
Maprs1049253
PheGenIrs1049253
hapmaprs1049253
1000 genomesrs1049253
hgdprs1049253
ensemblrs1049253
gopubmedrs1049253
geneviewrs1049253
scholarrs1049253
googlers1049253
pharmgkbrs1049253
gwascentralrs1049253
openSNPrs1049253
23andMers1049253
23andMe allrs1049253
SNP Nexus

SNPshotrs1049253
SNPdbers1049253
MSV3drs1049253
GWAS Ctlgrs1049253
GMAF0.08861
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23271051OA-icon.png] A functional variant at the miR-885-5p binding site of CASP3 confers risk of both index and second primary malignancies in patients with head and neck cancer


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


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