rs587782798

Orientation

plus

Stabilized

plus

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

Make rs587782798(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

68813322

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs587782798
dbSNP (classic)	rs587782798
ClinGen	rs587782798
ebi	rs587782798
HLI	rs587782798
Exac	rs587782798
Gnomad	rs587782798
Varsome	rs587782798
LitVar	rs587782798
Map	rs587782798
PheGenI	rs587782798
Biobank	rs587782798
1000 genomes	rs587782798
hgdp	rs587782798
ensembl	rs587782798
geneview	rs587782798
scholar	rs587782798
google	rs587782798
pharmgkb	rs587782798
gwascentral	rs587782798
openSNP	rs587782798
23andMe	rs587782798
SNPshot	rs587782798
SNPdbe	rs587782798
MSV3d	rs587782798
GWAS Ctlg	rs587782798

Max Magnitude

6.7

ClinVar
Risk	rs587782798(T;T)
Alt	rs587782798(T;T)
Reference	Rs587782798(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.68847225C>T
CLNSRC
CLNACC	RCV000132351.2,