rs786204893

Merged into

rs587782304

Orientation

plus

Stabilized

plus

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

Make rs786204893(-;-)

Make rs786204893(-;TAAA)

Make rs786204893(TAAA;TAAA)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87961079

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204893
dbSNP (classic)	rs786204893
ClinGen	rs786204893
ebi	rs786204893
HLI	rs786204893
Exac	rs786204893
Gnomad	rs786204893
Varsome	rs786204893
LitVar	rs786204893
Map	rs786204893
PheGenI	rs786204893
Biobank	rs786204893
1000 genomes	rs786204893
hgdp	rs786204893
ensembl	rs786204893
geneview	rs786204893
scholar	rs786204893
google	rs786204893
pharmgkb	rs786204893
gwascentral	rs786204893
openSNP	rs786204893
23andMe	rs786204893
SNPshot	rs786204893
SNPdbe	rs786204893
MSV3d	rs786204893
GWAS Ctlg	rs786204893

Status

Merged into rs587782304

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786204893(AAAT;AAAT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89720836_89720839delTAAA
CLNSRC
CLNACC	RCV000169834.3, RCV000212887.1,