rs121909220

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6.3	Lhermitte-Duclos disease

Make rs121909220(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87933228

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909220
dbSNP (classic)	rs121909220
ClinGen	rs121909220
ebi	rs121909220
HLI	rs121909220
Exac	rs121909220
Gnomad	rs121909220
Varsome	rs121909220
LitVar	rs121909220
Map	rs121909220
PheGenI	rs121909220
Biobank	rs121909220
1000 genomes	rs121909220
hgdp	rs121909220
ensembl	rs121909220
geneview	rs121909220
scholar	rs121909220
google	rs121909220
pharmgkb	rs121909220
gwascentral	rs121909220
openSNP	rs121909220
23andMe	rs121909220
SNPshot	rs121909220
SNPdbe	rs121909220
MSV3d	rs121909220
GWAS Ctlg	rs121909220

Max Magnitude

6.3

OMIM	601728
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909220(T;T)
Alt	rs121909220(T;T)
Reference	Rs121909220(G;G)
Significance	Pathogenic
Disease	Lhermitte-Duclos disease
Variation	info
Gene	PTEN
CLNDBN	Lhermitte-Duclos disease
Reversed	0
HGVS	NC_000010.10:g.89692985G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008258.2,