rs786204864

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.3	Bannayan-Riley-Ruvalcaba syndrome

Make rs786204864(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87952136

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204864
dbSNP (classic)	rs786204864
ClinGen	rs786204864
ebi	rs786204864
HLI	rs786204864
Exac	rs786204864
Gnomad	rs786204864
Varsome	rs786204864
LitVar	rs786204864
Map	rs786204864
PheGenI	rs786204864
Biobank	rs786204864
1000 genomes	rs786204864
hgdp	rs786204864
ensembl	rs786204864
geneview	rs786204864
scholar	rs786204864
google	rs786204864
pharmgkb	rs786204864
gwascentral	rs786204864
openSNP	rs786204864
23andMe	rs786204864
SNPshot	rs786204864
SNPdbe	rs786204864
MSV3d	rs786204864
GWAS Ctlg	rs786204864

Max Magnitude

6.3

ClinVar
Risk	rs786204864(T;T)
Alt	rs786204864(T;T)
Reference	Rs786204864(C;C)
Significance	Pathogenic
Disease	not provided PTEN hamartoma tumor syndrome Bannayan-Riley-Ruvalcaba syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided PTEN hamartoma tumor syndrome Bannayan-Riley-Ruvalcaba syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89711893C>T
CLNSRC
CLNACC	RCV000169804.2, RCV000233297.1, RCV000330369.1, RCV000491520.1,