rs1057520622

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common/normal
(A;T)	6.3	Hereditary cancer predisposing syndrome

Make rs1057520622(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

87933189

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1057520622
dbSNP (classic)	rs1057520622
ClinGen	rs1057520622
ebi	rs1057520622
HLI	rs1057520622
Exac	rs1057520622
Gnomad	rs1057520622
Varsome	rs1057520622
LitVar	rs1057520622
Map	rs1057520622
PheGenI	rs1057520622
Biobank	rs1057520622
1000 genomes	rs1057520622
hgdp	rs1057520622
ensembl	rs1057520622
geneview	rs1057520622
scholar	rs1057520622
google	rs1057520622
pharmgkb	rs1057520622
gwascentral	rs1057520622
openSNP	rs1057520622
23andMe	rs1057520622
SNPshot	rs1057520622
SNPdbe	rs1057520622
MSV3d	rs1057520622
GWAS Ctlg	rs1057520622

Max Magnitude

6.3

ClinVar
Risk	rs1057520622(T;T)
Alt	rs1057520622(T;T)
Reference	Rs1057520622(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTEN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.89692946A>T
CLNSRC
CLNACC	RCV000435296.1,