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rs1085308048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position87933175
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308048
dbSNP (classic)rs1085308048
ClinGenrs1085308048
ebirs1085308048
HLIrs1085308048
Exacrs1085308048
Gnomadrs1085308048
Varsomers1085308048
LitVarrs1085308048
Maprs1085308048
PheGenIrs1085308048
Biobankrs1085308048
1000 genomesrs1085308048
hgdprs1085308048
ensemblrs1085308048
geneviewrs1085308048
scholarrs1085308048
googlers1085308048
pharmgkbrs1085308048
gwascentralrs1085308048
openSNPrs1085308048
23andMers1085308048
23andMe allrs1085308048
SNPshotrs1085308048
SNPdbers1085308048
MSV3drs1085308048
GWAS Ctlgrs1085308048
Max Magnitude0
ClinVar
Risk rs1085308048(G;G)
Alt rs1085308048(G;G)
Reference Rs1085308048(T;T)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692932T>G
CLNSRC
CLNACC RCV000490603.1,