rs786204910

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.3	PTEN hamartoma tumor syndrome

Make rs786204910(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87864518

Gene	KLLN, PTEN

is a	snp
is	mentioned by
dbSNP	rs786204910
dbSNP (classic)	rs786204910
ClinGen	rs786204910
ebi	rs786204910
HLI	rs786204910
Exac	rs786204910
Gnomad	rs786204910
Varsome	rs786204910
LitVar	rs786204910
Map	rs786204910
PheGenI	rs786204910
Biobank	rs786204910
1000 genomes	rs786204910
hgdp	rs786204910
ensembl	rs786204910
geneview	rs786204910
scholar	rs786204910
google	rs786204910
pharmgkb	rs786204910
gwascentral	rs786204910
openSNP	rs786204910
23andMe	rs786204910
SNPshot	rs786204910
SNPdbe	rs786204910
MSV3d	rs786204910
GWAS Ctlg	rs786204910

Max Magnitude

6.3

ClinVar
Risk	rs786204910(T;T)
Alt	rs786204910(T;T)
Reference	Rs786204910(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN LOC101929706 KLLN
CLNDBN	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89624275C>T
CLNSRC
CLNACC	RCV000169851.2, RCV000204017.1,