rs1085308042

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

is a	snp
is	mentioned by
dbSNP	rs1085308042
dbSNP (classic)	rs1085308042
ClinGen	rs1085308042
ebi	rs1085308042
HLI	rs1085308042
Exac	rs1085308042
Gnomad	rs1085308042
Varsome	rs1085308042
LitVar	rs1085308042
Map	rs1085308042
PheGenI	rs1085308042
Biobank	rs1085308042
1000 genomes	rs1085308042
hgdp	rs1085308042
ensembl	rs1085308042
geneview	rs1085308042
scholar	rs1085308042
google	rs1085308042
pharmgkb	rs1085308042
gwascentral	rs1085308042
openSNP	rs1085308042
23andMe	rs1085308042
SNPshot	rs1085308042
SNPdbe	rs1085308042
MSV3d	rs1085308042
GWAS Ctlg	rs1085308042

Max Magnitude

0

ClinVar
Risk	rs1085308042(A;A)
Alt	rs1085308042(A;A)
Reference	Rs1085308042(G;G)
Significance	Pathogenic
Disease	PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89653833G>A
CLNSRC
CLNACC	RCV000490575.1,