rs121909241

Orientation

plus

Stabilized

plus

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

Make rs121909241(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87933154

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909241
dbSNP (classic)	rs121909241
ClinGen	rs121909241
ebi	rs121909241
HLI	rs121909241
Exac	rs121909241
Gnomad	rs121909241
Varsome	rs121909241
LitVar	rs121909241
Map	rs121909241
PheGenI	rs121909241
Biobank	rs121909241
1000 genomes	rs121909241
hgdp	rs121909241
ensembl	rs121909241
geneview	rs121909241
scholar	rs121909241
google	rs121909241
pharmgkb	rs121909241
gwascentral	rs121909241
openSNP	rs121909241
23andMe	rs121909241
SNPshot	rs121909241
SNPdbe	rs121909241
MSV3d	rs121909241
GWAS Ctlg	rs121909241

Max Magnitude

6.3

OMIM	601728
Desc
Variant	0041
Related	also

ClinVar
Risk	rs121909241(A;A) rs121909241(T;T)
Alt	rs121909241(A;A) rs121909241(T;T)
Reference	Rs121909241(G;G)
Significance	Pathogenic
Disease	not provided not specified PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided not specified PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692911G>A; NC_000010.10:g.89692911G>T
CLNSRC	HGMD OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000078616.6, RCV000259056.1, RCV000008302.2, RCV000221956.1, RCV000489810.1,