rs606231170

Orientation

plus

Stabilized

plus

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

Make rs606231170(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87952189

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs606231170
dbSNP (classic)	rs606231170
ClinGen	rs606231170
ebi	rs606231170
HLI	rs606231170
Exac	rs606231170
Gnomad	rs606231170
Varsome	rs606231170
LitVar	rs606231170
Map	rs606231170
PheGenI	rs606231170
Biobank	rs606231170
1000 genomes	rs606231170
hgdp	rs606231170
ensembl	rs606231170
geneview	rs606231170
scholar	rs606231170
google	rs606231170
pharmgkb	rs606231170
gwascentral	rs606231170
openSNP	rs606231170
23andMe	rs606231170
SNPshot	rs606231170
SNPdbe	rs606231170
MSV3d	rs606231170
GWAS Ctlg	rs606231170

Max Magnitude

6.3

ClinVar
Risk	rs606231170(A;A)
Alt	rs606231170(A;A)
Reference	Rs606231170(T;T)
Significance	Pathogenic
Disease	Prostate cancer
Variation	info
Gene	PTEN
CLNDBN	Prostate cancer, somatic
Reversed	0
HGVS	NC_000010.10:g.89711946T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008277.4,