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rs794729664

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729664(C;C)
Make rs794729664(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952170
GenePTEN
is asnp
is mentioned by
dbSNPrs794729664
ebirs794729664
HLIrs794729664
Exacrs794729664
Varsomers794729664
Maprs794729664
PheGenIrs794729664
hapmaprs794729664
1000 genomesrs794729664
hgdprs794729664
ensemblrs794729664
gopubmedrs794729664
geneviewrs794729664
scholarrs794729664
googlers794729664
pharmgkbrs794729664
gwascentralrs794729664
openSNPrs794729664
23andMers794729664
23andMe allrs794729664
SNP Nexus

SNPshotrs794729664
SNPdbers794729664
MSV3drs794729664
GWAS Ctlgrs794729664
Max Magnitude0
ClinVar
Risk rs794729664(C;C)
Alt rs794729664(C;C)
Reference rs794729664(T;T)
Significance Pathogenic
Disease Macrocephaly/autism syndrome
Variation info
Gene PTEN
CLNDBN Macrocephaly/autism syndrome
Reversed 0
HGVS NC_000010.10:g.89711927T>C
CLNSRC
CLNACC RCV000185586.1,