rs878853936

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6.3	PTEN hamartoma tumor syndrome

Make rs878853936(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87925543

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs878853936
dbSNP (classic)	rs878853936
ClinGen	rs878853936
ebi	rs878853936
HLI	rs878853936
Exac	rs878853936
Gnomad	rs878853936
Varsome	rs878853936
LitVar	rs878853936
Map	rs878853936
PheGenI	rs878853936
Biobank	rs878853936
1000 genomes	rs878853936
hgdp	rs878853936
ensembl	rs878853936
geneview	rs878853936
scholar	rs878853936
google	rs878853936
pharmgkb	rs878853936
gwascentral	rs878853936
openSNP	rs878853936
23andMe	rs878853936
SNPshot	rs878853936
SNPdbe	rs878853936
MSV3d	rs878853936
GWAS Ctlg	rs878853936

Max Magnitude

6.3

ClinVar
Risk	rs878853936(A;A) rs878853936(G;G)
Alt	rs878853936(A;A) rs878853936(G;G)
Reference	Rs878853936(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89685300C>A; NC_000010.10:g.89685300C>G
CLNSRC
CLNACC	RCV000490865.1, RCV000226814.1,