rs863224909

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs863224909(C;G)

Make rs863224909(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87960952

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs863224909
dbSNP (classic)	rs863224909
ClinGen	rs863224909
ebi	rs863224909
HLI	rs863224909
Exac	rs863224909
Gnomad	rs863224909
Varsome	rs863224909
LitVar	rs863224909
Map	rs863224909
PheGenI	rs863224909
Biobank	rs863224909
1000 genomes	rs863224909
hgdp	rs863224909
ensembl	rs863224909
geneview	rs863224909
scholar	rs863224909
google	rs863224909
pharmgkb	rs863224909
gwascentral	rs863224909
openSNP	rs863224909
23andMe	rs863224909
SNPshot	rs863224909
SNPdbe	rs863224909
MSV3d	rs863224909
GWAS Ctlg	rs863224909

Max Magnitude

0

ClinVar
Risk	rs863224909(A;A) rs863224909(G;G)
Alt	rs863224909(A;A) rs863224909(G;G)
Reference	Rs863224909(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome 1 Macrocephaly/autism syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome 1 Macrocephaly/autism syndrome
Reversed	0
HGVS	NC_000010.10:g.89720709C>A; NC_000010.10:g.89720709C>G
CLNSRC
CLNACC	RCV000491746.1, RCV000200784.1,