rs587781255

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.3	PTEN hamartoma tumor syndrome
(G;G)	0	common in clinvar

Make rs587781255(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87933138

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587781255
dbSNP (classic)	rs587781255
ClinGen	rs587781255
ebi	rs587781255
HLI	rs587781255
Exac	rs587781255
Gnomad	rs587781255
Varsome	rs587781255
LitVar	rs587781255
Map	rs587781255
PheGenI	rs587781255
Biobank	rs587781255
1000 genomes	rs587781255
hgdp	rs587781255
ensembl	rs587781255
geneview	rs587781255
scholar	rs587781255
google	rs587781255
pharmgkb	rs587781255
gwascentral	rs587781255
openSNP	rs587781255
23andMe	rs587781255
SNPshot	rs587781255
SNPdbe	rs587781255
MSV3d	rs587781255
GWAS Ctlg	rs587781255

Max Magnitude

6.3

ClinVar
Risk	rs587781255(A;A)
Alt	rs587781255(A;A)
Reference	Rs587781255(G;G)
Significance	Pathogenic
Disease	PTEN hamartoma tumor syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89692895G>A
CLNSRC
CLNACC	RCV000128454.1, RCV000479167.1,