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rs1064793243

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position87933082
GenePTEN
is asnp
is mentioned by
dbSNPrs1064793243
dbSNP (old)rs1064793243
ClinGenrs1064793243
ebirs1064793243
HLIrs1064793243
Exacrs1064793243
Gnomadrs1064793243
Varsomers1064793243
Maprs1064793243
PheGenIrs1064793243
Biobankrs1064793243
1000 genomesrs1064793243
hgdprs1064793243
ensemblrs1064793243
gopubmedrs1064793243
geneviewrs1064793243
scholarrs1064793243
googlers1064793243
pharmgkbrs1064793243
gwascentralrs1064793243
openSNPrs1064793243
23andMers1064793243
23andMe allrs1064793243
SNPshotrs1064793243
SNPdbers1064793243
MSV3drs1064793243
GWAS Ctlgrs1064793243
Max Magnitude0
ClinVar
Risk rs1064793243(C;C)
Alt rs1064793243(C;C)
Reference Rs1064793243(T;T)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692839T>C
CLNSRC
CLNACC RCV000479867.1, RCV000490832.1,