rs876661009

Orientation

plus

Stabilized

plus

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

Make rs876661009(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87864516

Gene	KLLN, PTEN

is a	snp
is	mentioned by
dbSNP	rs876661009
dbSNP (classic)	rs876661009
ClinGen	rs876661009
ebi	rs876661009
HLI	rs876661009
Exac	rs876661009
Gnomad	rs876661009
Varsome	rs876661009
LitVar	rs876661009
Map	rs876661009
PheGenI	rs876661009
Biobank	rs876661009
1000 genomes	rs876661009
hgdp	rs876661009
ensembl	rs876661009
geneview	rs876661009
scholar	rs876661009
google	rs876661009
pharmgkb	rs876661009
gwascentral	rs876661009
openSNP	rs876661009
23andMe	rs876661009
SNPshot	rs876661009
SNPdbe	rs876661009
MSV3d	rs876661009
GWAS Ctlg	rs876661009

Max Magnitude

6.3

ClinVar
Risk	rs876661009(A;A)
Alt	rs876661009(A;A)
Reference	Rs876661009(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTEN LOC101929706 KLLN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.89624273dupA
CLNSRC
CLNACC	RCV000221548.1,