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rs1085308041

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position87965285
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308041
dbSNP (old)rs1085308041
ClinGenrs1085308041
ebirs1085308041
HLIrs1085308041
Exacrs1085308041
Gnomadrs1085308041
Varsomers1085308041
Maprs1085308041
PheGenIrs1085308041
Biobankrs1085308041
1000 genomesrs1085308041
hgdprs1085308041
ensemblrs1085308041
gopubmedrs1085308041
geneviewrs1085308041
scholarrs1085308041
googlers1085308041
pharmgkbrs1085308041
gwascentralrs1085308041
openSNPrs1085308041
23andMers1085308041
23andMe allrs1085308041
SNPshotrs1085308041
SNPdbers1085308041
MSV3drs1085308041
GWAS Ctlgrs1085308041
Max Magnitude0
ClinVar
Risk rs1085308041(G;G)
Alt rs1085308041(G;G)
Reference Rs1085308041(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89725042A>G
CLNSRC
CLNACC RCV000490606.1, RCV000491514.1,