rs1057521060

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common/normal
(G;T)	6.3	Hereditary cancer predisposing syndrome

Make rs1057521060(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

87894110

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1057521060
dbSNP (classic)	rs1057521060
ClinGen	rs1057521060
ebi	rs1057521060
HLI	rs1057521060
Exac	rs1057521060
Gnomad	rs1057521060
Varsome	rs1057521060
LitVar	rs1057521060
Map	rs1057521060
PheGenI	rs1057521060
Biobank	rs1057521060
1000 genomes	rs1057521060
hgdp	rs1057521060
ensembl	rs1057521060
geneview	rs1057521060
scholar	rs1057521060
google	rs1057521060
pharmgkb	rs1057521060
gwascentral	rs1057521060
openSNP	rs1057521060
23andMe	rs1057521060
SNPshot	rs1057521060
SNPdbe	rs1057521060
MSV3d	rs1057521060
GWAS Ctlg	rs1057521060

Max Magnitude

6.3

ClinVar
Risk	rs1057521060(C;C) rs1057521060(T;T)
Alt	rs1057521060(C;C) rs1057521060(T;T)
Reference	Rs1057521060(G;G)
Significance	Pathogenic
Disease	PTEN hamartoma tumor syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89653867G>C; NC_000010.10:g.89653867G>T
CLNSRC
CLNACC	RCV000490591.1, RCV000433720.1, RCV000491416.1,