rs876658304

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;ATTT)	6.3	Hereditary cancer predisposing syndrome
(ATTT;ATTT)	0	common in clinvar

Make rs876658304(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87933217

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876658304
dbSNP (classic)	rs876658304
ClinGen	rs876658304
ebi	rs876658304
HLI	rs876658304
Exac	rs876658304
Gnomad	rs876658304
Varsome	rs876658304
LitVar	rs876658304
Map	rs876658304
PheGenI	rs876658304
Biobank	rs876658304
1000 genomes	rs876658304
hgdp	rs876658304
ensembl	rs876658304
geneview	rs876658304
scholar	rs876658304
google	rs876658304
pharmgkb	rs876658304
gwascentral	rs876658304
openSNP	rs876658304
23andMe	rs876658304
SNPshot	rs876658304
SNPdbe	rs876658304
MSV3d	rs876658304
GWAS Ctlg	rs876658304

Max Magnitude

6.3

ClinVar
Risk	rs876658304(-;-)
Alt	rs876658304(-;-)
Reference	Rs876658304(ATTT;ATTT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692974_89692977delATTT
CLNSRC
CLNACC	RCV000219850.1,