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rs587777796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777796(G;G)
Make rs587777796(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position179219719
GenePIK3CA
is asnp
is mentioned by
dbSNPrs587777796
ebirs587777796
HLIrs587777796
Exacrs587777796
Varsomers587777796
Maprs587777796
PheGenIrs587777796
hapmaprs587777796
1000 genomesrs587777796
hgdprs587777796
ensemblrs587777796
gopubmedrs587777796
geneviewrs587777796
scholarrs587777796
googlers587777796
pharmgkbrs587777796
gwascentralrs587777796
openSNPrs587777796
23andMers587777796
23andMe allrs587777796
SNP Nexus

SNPshotrs587777796
SNPdbers587777796
MSV3drs587777796
GWAS Ctlgrs587777796
Max Magnitude0
ClinVar
Risk rs587777796(G;G)
Alt rs587777796(G;G)
Reference rs587777796(T;T)
Significance Pathogenic
Disease Cowden syndrome 5
Variation info
Gene PIK3CA
CLNDBN Cowden syndrome 5
Reversed 0
HGVS NC_000003.11:g.178937507T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144512.2,