rs587781912

Orientation

plus

Stabilized

plus

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

Make rs587781912(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87864519

Gene	KLLN, PTEN

is a	snp
is	mentioned by
dbSNP	rs587781912
dbSNP (classic)	rs587781912
ClinGen	rs587781912
ebi	rs587781912
HLI	rs587781912
Exac	rs587781912
Gnomad	rs587781912
Varsome	rs587781912
LitVar	rs587781912
Map	rs587781912
PheGenI	rs587781912
Biobank	rs587781912
1000 genomes	rs587781912
hgdp	rs587781912
ensembl	rs587781912
geneview	rs587781912
scholar	rs587781912
google	rs587781912
pharmgkb	rs587781912
gwascentral	rs587781912
openSNP	rs587781912
23andMe	rs587781912
SNPshot	rs587781912
SNPdbe	rs587781912
MSV3d	rs587781912
GWAS Ctlg	rs587781912

Max Magnitude

6.3

ClinVar
Risk	rs587781912(-;-)
Alt	rs587781912(-;-)
Reference	Rs587781912(AA;AA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN LOC101929706 KLLN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89624276_89624277delAA
CLNSRC
CLNACC	RCV000130255.2, RCV000478451.1,