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rs121909236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909236(C;G)
Make rs121909236(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position87925529
GenePTEN
is asnp
is mentioned by
dbSNPrs121909236
ebirs121909236
HLIrs121909236
Exacrs121909236
Varsomers121909236
Maprs121909236
PheGenIrs121909236
hapmaprs121909236
1000 genomesrs121909236
hgdprs121909236
ensemblrs121909236
gopubmedrs121909236
geneviewrs121909236
scholarrs121909236
googlers121909236
pharmgkbrs121909236
gwascentralrs121909236
openSNPrs121909236
23andMers121909236
23andMe allrs121909236
SNP Nexus

SNPshotrs121909236
SNPdbers121909236
MSV3drs121909236
GWAS Ctlgrs121909236
Max Magnitude0
OMIM601728
Desc
Variant0030
Relatedalso
ClinVar
Risk rs121909236(G;G)
Alt rs121909236(G;G)
Reference rs121909236(C;C)
Significance Pathogenic
Disease Vater association with macrocephaly and ventriculomegaly
Variation info
Gene PTEN
CLNDBN Vater association with macrocephaly and ventriculomegaly
Reversed 0
HGVS NC_000010.10:g.89685286C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008290.2,