rs587782304

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TAAA)	6.3	Hereditary cancer predisposing syndrome
(AAAT;AAAT)	0	common in clinvar
(TAAA;TAAA)	0	common/normal

Make rs587782304(-;-)

Make rs587782304(-;AAAT)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87961076

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587782304
dbSNP (classic)	rs587782304
ClinGen	rs587782304
ebi	rs587782304
HLI	rs587782304
Exac	rs587782304
Gnomad	rs587782304
Varsome	rs587782304
LitVar	rs587782304
Map	rs587782304
PheGenI	rs587782304
Biobank	rs587782304
1000 genomes	rs587782304
hgdp	rs587782304
ensembl	rs587782304
geneview	rs587782304
scholar	rs587782304
google	rs587782304
pharmgkb	rs587782304
gwascentral	rs587782304
openSNP	rs587782304
23andMe	rs587782304
SNPshot	rs587782304
SNPdbe	rs587782304
MSV3d	rs587782304
GWAS Ctlg	rs587782304

Merged from

Rs786204893

Max Magnitude

6.3

ClinVar
Risk	rs587782304(-;-) Rs587782304(TAAA;TAAA)
Alt	rs587782304(-;-) Rs587782304(TAAA;TAAA)
Reference	Rs587782304(AAAT;AAAT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89720836_89720839delTAAA
CLNSRC
CLNACC	RCV000169834.3, RCV000212887.1,