rs398123315

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;A)	6.3	Hereditary cancer predisposing syndrome

Make rs398123315(A;A)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87965300

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs398123315
dbSNP (classic)	rs398123315
ClinGen	rs398123315
ebi	rs398123315
HLI	rs398123315
Exac	rs398123315
Gnomad	rs398123315
Varsome	rs398123315
LitVar	rs398123315
Map	rs398123315
PheGenI	rs398123315
Biobank	rs398123315
1000 genomes	rs398123315
hgdp	rs398123315
ensembl	rs398123315
geneview	rs398123315
scholar	rs398123315
google	rs398123315
pharmgkb	rs398123315
gwascentral	rs398123315
openSNP	rs398123315
23andMe	rs398123315
SNPshot	rs398123315
SNPdbe	rs398123315
MSV3d	rs398123315
GWAS Ctlg	rs398123315

Max Magnitude

6.3

ClinVar
Risk	rs398123315(A;A)
Alt	rs398123315(A;A)
Reference	Rs398123315(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTEN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.89725057_89725058insA
CLNSRC	ClinVar
CLNACC	RCV000078605.3,