rs121909238

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6.3	Macrocephaly/autism syndrome

Make rs121909238(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87933037

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909238
dbSNP (classic)	rs121909238
ClinGen	rs121909238
ebi	rs121909238
HLI	rs121909238
Exac	rs121909238
Gnomad	rs121909238
Varsome	rs121909238
LitVar	rs121909238
Map	rs121909238
PheGenI	rs121909238
Biobank	rs121909238
1000 genomes	rs121909238
hgdp	rs121909238
ensembl	rs121909238
geneview	rs121909238
scholar	rs121909238
google	rs121909238
pharmgkb	rs121909238
gwascentral	rs121909238
openSNP	rs121909238
23andMe	rs121909238
SNPshot	rs121909238
SNPdbe	rs121909238
MSV3d	rs121909238
GWAS Ctlg	rs121909238

Max Magnitude

6.3

OMIM	601728
Desc
Variant	0037
Related	also

ClinVar
Risk	rs121909238(G;G)
Alt	rs121909238(G;G)
Reference	Rs121909238(A;A)
Significance	Pathogenic
Disease	Macrocephaly/autism syndrome
Variation	info
Gene	PTEN
CLNDBN	Macrocephaly/autism syndrome
Reversed	0
HGVS	NC_000010.10:g.89692794A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008298.2,