rs116093741

Orientation

plus

Stabilized

plus

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

Make rs116093741(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

68812144

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs116093741
dbSNP (classic)	rs116093741
ClinGen	rs116093741
ebi	rs116093741
HLI	rs116093741
Exac	rs116093741
Gnomad	rs116093741
Varsome	rs116093741
LitVar	rs116093741
Map	rs116093741
PheGenI	rs116093741
Biobank	rs116093741
1000 genomes	rs116093741
hgdp	rs116093741
ensembl	rs116093741
geneview	rs116093741
scholar	rs116093741
google	rs116093741
pharmgkb	rs116093741
gwascentral	rs116093741
openSNP	rs116093741
23andMe	rs116093741
SNPshot	rs116093741
SNPdbe	rs116093741
MSV3d	rs116093741
GWAS Ctlg	rs116093741

GMAF

0.0004591

Max Magnitude

5

OMIM	192090
Desc
Variant	0016
Related	also

ClinVar
Risk	rs116093741(G;G) rs116093741(T;T)
Alt	rs116093741(G;G) rs116093741(T;T)
Reference	Rs116093741(A;A)
Significance	Other
Disease	Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	CDH1
CLNDBN	Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000016.9:g.68846047A>G; NC_000016.9:g.68846047A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013032.29, RCV000115833.5, RCV000212359.1, RCV000478241.1,