rs786204881

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GA)	6.3	Hereditary cancer predisposing syndrome
(AG;AG)	0	common in clinvar
(GA;GA)	0	common/normal

Make rs786204881(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87864490

Gene	KLLN, PTEN

is a	snp
is	mentioned by
dbSNP	rs786204881
dbSNP (classic)	rs786204881
ClinGen	rs786204881
ebi	rs786204881
HLI	rs786204881
Exac	rs786204881
Gnomad	rs786204881
Varsome	rs786204881
LitVar	rs786204881
Map	rs786204881
PheGenI	rs786204881
Biobank	rs786204881
1000 genomes	rs786204881
hgdp	rs786204881
ensembl	rs786204881
geneview	rs786204881
scholar	rs786204881
google	rs786204881
pharmgkb	rs786204881
gwascentral	rs786204881
openSNP	rs786204881
23andMe	rs786204881
SNPshot	rs786204881
SNPdbe	rs786204881
MSV3d	rs786204881
GWAS Ctlg	rs786204881

Max Magnitude

6.3

ClinVar
Risk	rs786204881(-;-)
Alt	rs786204881(-;-)
Reference	Rs786204881(AG;AG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN LOC101929706 KLLN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89624247_89624248delGA
CLNSRC
CLNACC	RCV000169822.1,