rs121909234

Orientation

plus

Stabilized

plus

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

Make rs121909234(A;A)

Make rs121909234(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87957867

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121909234
dbSNP (classic)	rs121909234
ClinGen	rs121909234
ebi	rs121909234
HLI	rs121909234
Exac	rs121909234
Gnomad	rs121909234
Varsome	rs121909234
LitVar	rs121909234
Map	rs121909234
PheGenI	rs121909234
Biobank	rs121909234
1000 genomes	rs121909234
hgdp	rs121909234
ensembl	rs121909234
geneview	rs121909234
scholar	rs121909234
google	rs121909234
pharmgkb	rs121909234
gwascentral	rs121909234
openSNP	rs121909234
23andMe	rs121909234
SNPshot	rs121909234
SNPdbe	rs121909234
MSV3d	rs121909234
GWAS Ctlg	rs121909234

Max Magnitude

0

OMIM	601728
Desc
Variant	0026
Related	also

ClinVar
Risk	rs121909234(A;A)
Alt	rs121909234(A;A)
Reference	Rs121909234(G;G)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	PTEN
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000010.10:g.89717624G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008286.5,