rs587776665

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(I;I)	0	common genotype
(TG;TG)	0	common in clinvar

Make rs587776665(-;-)

Make rs587776665(-;GT)

Make rs587776665(GT;GT)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

201285241

Gene

CASP8

is a	snp
is	mentioned by
dbSNP	rs587776665
dbSNP (classic)	rs587776665
ClinGen	rs587776665
ebi	rs587776665
HLI	rs587776665
Exac	rs587776665
Gnomad	rs587776665
Varsome	rs587776665
LitVar	rs587776665
Map	rs587776665
PheGenI	rs587776665
Biobank	rs587776665
1000 genomes	rs587776665
hgdp	rs587776665
ensembl	rs587776665
geneview	rs587776665
scholar	rs587776665
google	rs587776665
pharmgkb	rs587776665
gwascentral	rs587776665
openSNP	rs587776665
23andMe	rs587776665
SNPshot	rs587776665
SNPdbe	rs587776665
MSV3d	rs587776665
GWAS Ctlg	rs587776665

Max Magnitude

0

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,