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rs863224909

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224909(C;G)
Make rs863224909(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960952
GenePTEN
is asnp
is mentioned by
dbSNPrs863224909
ebirs863224909
HLIrs863224909
Exacrs863224909
Varsomers863224909
Maprs863224909
PheGenIrs863224909
hapmaprs863224909
1000 genomesrs863224909
hgdprs863224909
ensemblrs863224909
gopubmedrs863224909
geneviewrs863224909
scholarrs863224909
googlers863224909
pharmgkbrs863224909
gwascentralrs863224909
openSNPrs863224909
23andMers863224909
23andMe allrs863224909
SNP Nexus

SNPshotrs863224909
SNPdbers863224909
MSV3drs863224909
GWAS Ctlgrs863224909
Max Magnitude0
ClinVar
Risk rs863224909(G;G)
Alt rs863224909(G;G)
Reference rs863224909(C;C)
Significance Probable-Pathogenic
Disease Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome 1 Macrocephaly/autism syndrome
Variation info
Gene PTEN
CLNDBN Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome 1 Macrocephaly/autism syndrome
Reversed 0
HGVS NC_000010.10:g.89720709C>G
CLNSRC
CLNACC RCV000200784.1,