rs121909776

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121909776(C;C)

Make rs121909776(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

201187798

Gene

CASP10

is a	snp
is	mentioned by
dbSNP	rs121909776
dbSNP (classic)	rs121909776
ClinGen	rs121909776
ebi	rs121909776
HLI	rs121909776
Exac	rs121909776
Gnomad	rs121909776
Varsome	rs121909776
LitVar	rs121909776
Map	rs121909776
PheGenI	rs121909776
Biobank	rs121909776
1000 genomes	rs121909776
hgdp	rs121909776
ensembl	rs121909776
geneview	rs121909776
scholar	rs121909776
google	rs121909776
pharmgkb	rs121909776
gwascentral	rs121909776
openSNP	rs121909776
23andMe	rs121909776
SNPshot	rs121909776
SNPdbe	rs121909776
MSV3d	rs121909776
GWAS Ctlg	rs121909776

GMAF

0.0004591

Max Magnitude

0

OMIM	601762
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909776(C;C)
Alt	rs121909776(C;C)
Reference	Rs121909776(T;T)
Significance	Pathogenic
Disease	Neoplasm of stomach
Variation	info
Gene	CASP10
CLNDBN	Neoplasm of stomach
Reversed	0
HGVS	NC_000002.11:g.202052521T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008210.5,