rs121909237

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs121909237(C;G)

Make rs121909237(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87933121

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909237
dbSNP (classic)	rs121909237
ClinGen	rs121909237
ebi	rs121909237
HLI	rs121909237
Exac	rs121909237
Gnomad	rs121909237
Varsome	rs121909237
LitVar	rs121909237
Map	rs121909237
PheGenI	rs121909237
Biobank	rs121909237
1000 genomes	rs121909237
hgdp	rs121909237
ensembl	rs121909237
geneview	rs121909237
scholar	rs121909237
google	rs121909237
pharmgkb	rs121909237
gwascentral	rs121909237
openSNP	rs121909237
23andMe	rs121909237
SNPshot	rs121909237
SNPdbe	rs121909237
MSV3d	rs121909237
GWAS Ctlg	rs121909237

Max Magnitude

0

OMIM	601728
Desc
Variant	0031
Related	also

ClinVar
Risk	rs121909237(G;G)
Alt	rs121909237(G;G)
Reference	Rs121909237(C;C)
Significance	Pathogenic
Disease	Squamous cell carcinoma of the head and neck
Variation	info
Gene	PTEN
CLNDBN	Squamous cell carcinoma of the head and neck
Reversed	0
HGVS	NC_000010.10:g.89692878C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008291.5,