rs587782750

Orientation

plus

Stabilized

plus

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

Make rs587782750(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

68822210

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs587782750
dbSNP (classic)	rs587782750
ClinGen	rs587782750
ebi	rs587782750
HLI	rs587782750
Exac	rs587782750
Gnomad	rs587782750
Varsome	rs587782750
LitVar	rs587782750
Map	rs587782750
PheGenI	rs587782750
Biobank	rs587782750
1000 genomes	rs587782750
hgdp	rs587782750
ensembl	rs587782750
geneview	rs587782750
scholar	rs587782750
google	rs587782750
pharmgkb	rs587782750
gwascentral	rs587782750
openSNP	rs587782750
23andMe	rs587782750
SNPshot	rs587782750
SNPdbe	rs587782750
MSV3d	rs587782750
GWAS Ctlg	rs587782750

Max Magnitude

5

ClinVar
Risk	rs587782750(T;T)
Alt	rs587782750(T;T)
Reference	Rs587782750(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.68856113C>T
CLNSRC
CLNACC	RCV000132257.2,