rs121909775

Orientation

plus

Stabilized

plus

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

Make rs121909775(C;T)

Make rs121909775(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

201205929

Gene

CASP10

is a	snp
is	mentioned by
dbSNP	rs121909775
dbSNP (classic)	rs121909775
ClinGen	rs121909775
ebi	rs121909775
HLI	rs121909775
Exac	rs121909775
Gnomad	rs121909775
Varsome	rs121909775
LitVar	rs121909775
Map	rs121909775
PheGenI	rs121909775
Biobank	rs121909775
1000 genomes	rs121909775
hgdp	rs121909775
ensembl	rs121909775
geneview	rs121909775
scholar	rs121909775
google	rs121909775
pharmgkb	rs121909775
gwascentral	rs121909775
openSNP	rs121909775
23andMe	rs121909775
SNPshot	rs121909775
SNPdbe	rs121909775
MSV3d	rs121909775
GWAS Ctlg	rs121909775

Max Magnitude

0

OMIM	601762
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909775(A;A) rs121909775(T;T)
Alt	rs121909775(A;A) rs121909775(T;T)
Reference	Rs121909775(C;C)
Significance	Pathogenic
Disease	Malignant lymphoma Neoplasm of stomach
Variation	info
Gene	CASP10
CLNDBN	Malignant lymphoma, non-Hodgkin Neoplasm of stomach
Reversed	0
HGVS	NC_000002.11:g.202070652C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008207.5, RCV000008208.5,