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rs1057521060

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 6.3 Hereditary cancer predisposing syndrome
Make rs1057521060(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87894110
GenePTEN
is asnp
is mentioned by
dbSNPrs1057521060
dbSNP (old)rs1057521060
ClinGenrs1057521060
ebirs1057521060
HLIrs1057521060
Exacrs1057521060
Gnomadrs1057521060
Varsomers1057521060
Maprs1057521060
PheGenIrs1057521060
Biobankrs1057521060
1000 genomesrs1057521060
hgdprs1057521060
ensemblrs1057521060
gopubmedrs1057521060
geneviewrs1057521060
scholarrs1057521060
googlers1057521060
pharmgkbrs1057521060
gwascentralrs1057521060
openSNPrs1057521060
23andMers1057521060
23andMe allrs1057521060
SNPshotrs1057521060
SNPdbers1057521060
MSV3drs1057521060
GWAS Ctlgrs1057521060
Max Magnitude6.3
ClinVar
Risk rs1057521060(C;C) rs1057521060(T;T)
Alt rs1057521060(C;C) rs1057521060(T;T)
Reference Rs1057521060(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89653867G>C; NC_000010.10:g.89653867G>T
CLNSRC
CLNACC RCV000490591.1, RCV000433720.1, RCV000491416.1,