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rs1085308049

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position87957885
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308049
dbSNP (old)rs1085308049
ClinGenrs1085308049
ebirs1085308049
HLIrs1085308049
Exacrs1085308049
Gnomadrs1085308049
Varsomers1085308049
Maprs1085308049
PheGenIrs1085308049
Biobankrs1085308049
1000 genomesrs1085308049
hgdprs1085308049
ensemblrs1085308049
gopubmedrs1085308049
geneviewrs1085308049
scholarrs1085308049
googlers1085308049
pharmgkbrs1085308049
gwascentralrs1085308049
openSNPrs1085308049
23andMers1085308049
23andMe allrs1085308049
SNPshotrs1085308049
SNPdbers1085308049
MSV3drs1085308049
GWAS Ctlgrs1085308049
Max Magnitude0
ClinVar
Risk rs1085308049(T;T)
Alt rs1085308049(T;T)
Reference Rs1085308049(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89717642A>T
CLNSRC
CLNACC RCV000490615.1,