rs104894184

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs104894184(A;A)

Make rs104894184(A;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

87952159

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs104894184
dbSNP (classic)	rs104894184
ClinGen	rs104894184
ebi	rs104894184
HLI	rs104894184
Exac	rs104894184
Gnomad	rs104894184
Varsome	rs104894184
LitVar	rs104894184
Map	rs104894184
PheGenI	rs104894184
Biobank	rs104894184
1000 genomes	rs104894184
hgdp	rs104894184
ensembl	rs104894184
geneview	rs104894184
scholar	rs104894184
google	rs104894184
pharmgkb	rs104894184
gwascentral	rs104894184
openSNP	rs104894184
23andMe	rs104894184
SNPshot	rs104894184
SNPdbe	rs104894184
MSV3d	rs104894184
GWAS Ctlg	rs104894184

Max Magnitude

0

OMIM	601728
Desc
Variant	0014
Related	also

ClinVar
Risk	rs104894184(A;A) rs104894184(C;C) rs104894184(G;G)
Alt	rs104894184(A;A) rs104894184(C;C) rs104894184(G;G)
Reference	Rs104894184(T;T)
Significance	Probable-non-pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89711916T>C
CLNSRC
CLNACC	RCV000220500.1,