rs786201045

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AG)	5	Hereditary cancer-predisposing syndrome; gastric cancer related?
(AG;AG)	0	common in clinvar

Make rs786201045(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

68812135

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs786201045
dbSNP (classic)	rs786201045
ClinGen	rs786201045
ebi	rs786201045
HLI	rs786201045
Exac	rs786201045
Gnomad	rs786201045
Varsome	rs786201045
LitVar	rs786201045
Map	rs786201045
PheGenI	rs786201045
Biobank	rs786201045
1000 genomes	rs786201045
hgdp	rs786201045
ensembl	rs786201045
geneview	rs786201045
scholar	rs786201045
google	rs786201045
pharmgkb	rs786201045
gwascentral	rs786201045
openSNP	rs786201045
23andMe	rs786201045
SNPshot	rs786201045
SNPdbe	rs786201045
MSV3d	rs786201045
GWAS Ctlg	rs786201045

Max Magnitude

5

Also known as c.1009_1010delAG, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk	rs786201045(-;-)
Alt	rs786201045(-;-)
Reference	Rs786201045(AG;AG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.68846038_68846039delAG
CLNSRC
CLNACC	RCV000162429.1,