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rs3769823

From SNPedia

Orientationminus
Stabilizedminus
Make rs3769823(C;C)
Make rs3769823(C;T)
Make rs3769823(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position201258272
GeneCASP8
is asnp
is mentioned by
dbSNPrs3769823
ClinGenrs3769823
ebirs3769823
HLIrs3769823
Exacrs3769823
Varsomers3769823
Maprs3769823
PheGenIrs3769823
hapmaprs3769823
1000 genomesrs3769823
hgdprs3769823
ensemblrs3769823
gopubmedrs3769823
geneviewrs3769823
scholarrs3769823
googlers3769823
pharmgkbrs3769823
gwascentralrs3769823
openSNPrs3769823
23andMers3769823
23andMe allrs3769823
SNP Nexus

SNPshotrs3769823
SNPdbers3769823
MSV3drs3769823
GWAS Ctlgrs3769823
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26635288OA-icon.png] Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.


[PMID 28177523] Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.


[PMID 28542283] Shared susceptibility loci at 2q33 region for lung and esophageal cancers in high-incidence areas of esophageal cancer in northern China.


ClinVar
Risk rs3769823(C;C)
Alt rs3769823(C;C)
Reference rs3769823(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CASP8
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.202122995A>G
CLNSRC
CLNACC RCV000455301.1,