rs587776668

Orientation

plus

Stabilized

plus

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

Make rs587776668(G;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87933253

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776668
dbSNP (classic)	rs587776668
ClinGen	rs587776668
ebi	rs587776668
HLI	rs587776668
Exac	rs587776668
Gnomad	rs587776668
Varsome	rs587776668
LitVar	rs587776668
Map	rs587776668
PheGenI	rs587776668
Biobank	rs587776668
1000 genomes	rs587776668
hgdp	rs587776668
ensembl	rs587776668
geneview	rs587776668
scholar	rs587776668
google	rs587776668
pharmgkb	rs587776668
gwascentral	rs587776668
openSNP	rs587776668
23andMe	rs587776668
SNPshot	rs587776668
SNPdbe	rs587776668
MSV3d	rs587776668
GWAS Ctlg	rs587776668

Max Magnitude

6.3

ClinVar
Risk	rs587776668(C;C) rs587776668(G;G)
Alt	rs587776668(C;C) rs587776668(G;G)
Reference	Rs587776668(T;T)
Significance	Pathogenic
Disease	not provided Cowden syndrome 1
Variation	info
Gene	PTEN
CLNDBN	not provided Cowden syndrome 1
Reversed	0
HGVS	NC_000010.10:g.89693010T>C; NC_000010.10:g.89693010T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000213348.1, RCV000008267.4,