rs746930141

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6.3	Hereditary cancer predisposing syndrome

Make rs746930141(C;C)

Make rs746930141(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87961011

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs746930141
dbSNP (classic)	rs746930141
ClinGen	rs746930141
ebi	rs746930141
HLI	rs746930141
Exac	rs746930141
Gnomad	rs746930141
Varsome	rs746930141
LitVar	rs746930141
Map	rs746930141
PheGenI	rs746930141
Biobank	rs746930141
1000 genomes	rs746930141
hgdp	rs746930141
ensembl	rs746930141
geneview	rs746930141
scholar	rs746930141
google	rs746930141
pharmgkb	rs746930141
gwascentral	rs746930141
openSNP	rs746930141
23andMe	rs746930141
SNPshot	rs746930141
SNPdbe	rs746930141
MSV3d	rs746930141
GWAS Ctlg	rs746930141

Max Magnitude

6.3

ClinVar
Risk	rs746930141(C;C) rs746930141(T;T)
Alt	rs746930141(C;C) rs746930141(T;T)
Reference	Rs746930141(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89720768G>C; NC_000010.10:g.89720768G>T
CLNSRC
CLNACC	RCV000164957.1, RCV000169816.2,