rs587776398

plus

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

Make rs587776398(G;G)

Reference

GRCh38 38.1/142

Chromosome

16

Position

68812149

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs587776398
dbSNP (classic)	rs587776398
ClinGen	rs587776398
ebi	rs587776398
HLI	rs587776398
Exac	rs587776398
Gnomad	rs587776398
Varsome	rs587776398
LitVar	rs587776398
Map	rs587776398
PheGenI	rs587776398
Biobank	rs587776398
1000 genomes	rs587776398
hgdp	rs587776398
ensembl	rs587776398
geneview	rs587776398
scholar	rs587776398
google	rs587776398
pharmgkb	rs587776398
gwascentral	rs587776398
openSNP	rs587776398
23andMe	rs587776398
SNPshot	rs587776398
SNPdbe	rs587776398
MSV3d	rs587776398
GWAS Ctlg	rs587776398

Max Magnitude

6.7

Also known as c.1023T>G, p.Tyr341Ter or Y341X, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk	rs587776398(C;C) rs587776398(G;G)
Alt	rs587776398(C;C) rs587776398(G;G)
Reference	Rs587776398(T;T)
Significance	Pathogenic
Disease	Hereditary diffuse gastric cancer
Variation	info
Gene	CDH1
CLNDBN	Hereditary diffuse gastric cancer
Reversed	0
HGVS	NC_000016.9:g.68846052T>C; NC_000016.9:g.68846052T>G
CLNSRC	ClinVar
CLNACC	RCV000229435.3, RCV000144456.1,