rs121909235

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.8	Glioma susceptibility; meningioma (indicated
(G;G)	0	common in complete genomics

Make rs121909235(A;A)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87957919

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909235
dbSNP (classic)	rs121909235
ClinGen	rs121909235
ebi	rs121909235
HLI	rs121909235
Exac	rs121909235
Gnomad	rs121909235
Varsome	rs121909235
LitVar	rs121909235
Map	rs121909235
PheGenI	rs121909235
Biobank	rs121909235
1000 genomes	rs121909235
hgdp	rs121909235
ensembl	rs121909235
geneview	rs121909235
scholar	rs121909235
google	rs121909235
pharmgkb	rs121909235
gwascentral	rs121909235
openSNP	rs121909235
23andMe	rs121909235
SNPshot	rs121909235
SNPdbe	rs121909235
MSV3d	rs121909235
GWAS Ctlg	rs121909235

Max Magnitude

6.8

OMIM	601728
Desc
Variant	0029
Related	also

ClinVar
Risk	rs121909235(A;A)
Alt	rs121909235(A;A)
Reference	Rs121909235(G;G)
Significance	Other
Disease	Glioma susceptibility 2 Meningioma
Variation	info
Gene	PTEN
CLNDBN	Glioma susceptibility 2 Meningioma
Reversed	0
HGVS	NC_000010.10:g.89717676G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008288.2, RCV000008289.2,