rs786203727

Orientation

plus

Stabilized

plus

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

Make rs786203727(G;T)

Make rs786203727(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

68801691

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs786203727
dbSNP (classic)	rs786203727
ClinGen	rs786203727
ebi	rs786203727
HLI	rs786203727
Exac	rs786203727
Gnomad	rs786203727
Varsome	rs786203727
LitVar	rs786203727
Map	rs786203727
PheGenI	rs786203727
Biobank	rs786203727
1000 genomes	rs786203727
hgdp	rs786203727
ensembl	rs786203727
geneview	rs786203727
scholar	rs786203727
google	rs786203727
pharmgkb	rs786203727
gwascentral	rs786203727
openSNP	rs786203727
23andMe	rs786203727
SNPshot	rs786203727
SNPdbe	rs786203727
MSV3d	rs786203727
GWAS Ctlg	rs786203727

Max Magnitude

0

ClinVar
Risk	rs786203727(T;T)
Alt	rs786203727(T;T)
Reference	Rs786203727(G;G)
Significance	Unknown
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.68835594G>T
CLNSRC
CLNACC	RCV000167156.1,