rs375709098

Orientation

plus

Stabilized

plus

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

Make rs375709098(C;T)

Make rs375709098(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87965321

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs375709098
dbSNP (classic)	rs375709098
ClinGen	rs375709098
ebi	rs375709098
HLI	rs375709098
Exac	rs375709098
Gnomad	rs375709098
Varsome	rs375709098
LitVar	rs375709098
Map	rs375709098
PheGenI	rs375709098
Biobank	rs375709098
1000 genomes	rs375709098
hgdp	rs375709098
ensembl	rs375709098
geneview	rs375709098
scholar	rs375709098
google	rs375709098
pharmgkb	rs375709098
gwascentral	rs375709098
openSNP	rs375709098
23andMe	rs375709098
SNPshot	rs375709098
SNPdbe	rs375709098
MSV3d	rs375709098
GWAS Ctlg	rs375709098

Max Magnitude

0

ClinVar
Risk	rs375709098(A;A) rs375709098(T;T)
Alt	rs375709098(A;A) rs375709098(T;T)
Reference	Rs375709098(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified PTEN hamartoma tumor syndrome Inborn genetic diseases Cowden syndrome 1
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not specified PTEN hamartoma tumor syndrome Inborn genetic diseases Cowden syndrome 1
Reversed	0
HGVS	NC_000010.10:g.89725078C>A; NC_000010.10:g.89725078C>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000132539.4, RCV000201314.2, RCV000205690.2, RCV000210607.1, RCV000409006.1, RCV000131204.2, RCV000180490.1, RCV000469633.1,