rs869312764

Merged into

rs863224505

Orientation

plus

Stabilized

plus

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

Make rs869312764(-;-)

Make rs869312764(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

68812190

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs869312764
dbSNP (classic)	rs869312764
ClinGen	rs869312764
ebi	rs869312764
HLI	rs869312764
Exac	rs869312764
Gnomad	rs869312764
Varsome	rs869312764
LitVar	rs869312764
Map	rs869312764
PheGenI	rs869312764
Biobank	rs869312764
1000 genomes	rs869312764
hgdp	rs869312764
ensembl	rs869312764
geneview	rs869312764
scholar	rs869312764
google	rs869312764
pharmgkb	rs869312764
gwascentral	rs869312764
openSNP	rs869312764
23andMe	rs869312764
SNPshot	rs869312764
SNPdbe	rs869312764
MSV3d	rs869312764
GWAS Ctlg	rs869312764

Status

Merged into rs863224505

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs869312764(T;T)
Significance	Pathogenic
Disease	Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDH1
CLNDBN	Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.68846093delT
CLNSRC
CLNACC	RCV000196464.1, RCV000210107.1,