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rs587777793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777793(A;A)
Make rs587777793(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position179204509
GenePIK3CA
is asnp
is mentioned by
dbSNPrs587777793
ebirs587777793
HLIrs587777793
Exacrs587777793
Varsomers587777793
Maprs587777793
PheGenIrs587777793
hapmaprs587777793
1000 genomesrs587777793
hgdprs587777793
ensemblrs587777793
gopubmedrs587777793
geneviewrs587777793
scholarrs587777793
googlers587777793
pharmgkbrs587777793
gwascentralrs587777793
openSNPrs587777793
23andMers587777793
23andMe allrs587777793
SNP Nexus

SNPshotrs587777793
SNPdbers587777793
MSV3drs587777793
GWAS Ctlgrs587777793
Max Magnitude0
ClinVar
Risk rs587777793(A;A)
Alt rs587777793(A;A)
Reference rs587777793(G;G)
Significance Pathogenic
Disease Cowden syndrome 5
Variation info
Gene PIK3CA
CLNDBN Cowden syndrome 5
Reversed 0
HGVS NC_000003.11:g.178922297G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144509.2,