rs587781276

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TG)	6.7	CDH1-based gastric cancer risk
(TG;TG)	0	common in clinvar

Make rs587781276(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

68823526

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs587781276
dbSNP (classic)	rs587781276
ClinGen	rs587781276
ebi	rs587781276
HLI	rs587781276
Exac	rs587781276
Gnomad	rs587781276
Varsome	rs587781276
LitVar	rs587781276
Map	rs587781276
PheGenI	rs587781276
Biobank	rs587781276
1000 genomes	rs587781276
hgdp	rs587781276
ensembl	rs587781276
geneview	rs587781276
scholar	rs587781276
google	rs587781276
pharmgkb	rs587781276
gwascentral	rs587781276
openSNP	rs587781276
23andMe	rs587781276
SNPshot	rs587781276
SNPdbe	rs587781276
MSV3d	rs587781276
GWAS Ctlg	rs587781276

Merged from

Rs786204165

Max Magnitude

6.7

Also known as c.2064_2065delTG, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk	rs587781276(-;-)
Alt	rs587781276(-;-)
Reference	Rs587781276(TG;TG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Variation	info
Gene	CDH1
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Reversed	0
HGVS	NC_000016.9:g.68857429_68857430delTG
CLNSRC
CLNACC	RCV000128928.2, RCV000168178.1,