rs727504114

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	6.3	Cowden syndrome (PTEN hamartoma tumor syndrome)
(G;T)	6.3	Hereditary cancer predisposing syndrome
(T;T)	0	common in clinvar

Make rs727504114(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87952261

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs727504114
dbSNP (classic)	rs727504114
ClinGen	rs727504114
ebi	rs727504114
HLI	rs727504114
Exac	rs727504114
Gnomad	rs727504114
Varsome	rs727504114
LitVar	rs727504114
Map	rs727504114
PheGenI	rs727504114
Biobank	rs727504114
1000 genomes	rs727504114
hgdp	rs727504114
ensembl	rs727504114
geneview	rs727504114
scholar	rs727504114
google	rs727504114
pharmgkb	rs727504114
gwascentral	rs727504114
openSNP	rs727504114
23andMe	rs727504114
SNPshot	rs727504114
SNPdbe	rs727504114
MSV3d	rs727504114
GWAS Ctlg	rs727504114

Max Magnitude

6.3

ClinVar
Risk	rs727504114(G;G)
Alt	rs727504114(G;G)
Reference	Rs727504114(T;T)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89712018T>G
CLNSRC	HGMD
CLNACC	RCV000153791.3, RCV000491022.1,