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rs587776665

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587776665(-;-)
Make rs587776665(-;GT)
Make rs587776665(GT;GT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201285241
GeneCASP8
is asnp
is mentioned by
dbSNPrs587776665
ebirs587776665
HLIrs587776665
Exacrs587776665
Varsomers587776665
Maprs587776665
PheGenIrs587776665
hapmaprs587776665
1000 genomesrs587776665
hgdprs587776665
ensemblrs587776665
gopubmedrs587776665
geneviewrs587776665
scholarrs587776665
googlers587776665
pharmgkbrs587776665
gwascentralrs587776665
openSNPrs587776665
23andMers587776665
23andMe allrs587776665
SNP Nexus

SNPshotrs587776665
SNPdbers587776665
MSV3drs587776665
GWAS Ctlgrs587776665
Max Magnitude0
ClinVar
Risk rs587776665(;)
Alt rs587776665(;)
Reference rs587776665(TG;TG)
Significance Pathogenic
Disease Hepatocellular carcinoma
Variation info
Gene CASP8
CLNDBN Hepatocellular carcinoma
Reversed 0
HGVS NC_000002.11:g.202149964_202149965delGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008202.5,