Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777794(A;A)
Make rs587777794(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position179204588
GenePIK3CA
is asnp
is mentioned by
dbSNPrs587777794
ebirs587777794
HLIrs587777794
Exacrs587777794
Varsomers587777794
Maprs587777794
PheGenIrs587777794
hapmaprs587777794
1000 genomesrs587777794
hgdprs587777794
ensemblrs587777794
gopubmedrs587777794
geneviewrs587777794
scholarrs587777794
googlers587777794
pharmgkbrs587777794
gwascentralrs587777794
openSNPrs587777794
23andMers587777794
23andMe allrs587777794
SNP Nexus

SNPshotrs587777794
SNPdbers587777794
MSV3drs587777794
GWAS Ctlgrs587777794
Max Magnitude0
ClinVar
Risk rs587777794(A;A)
Alt rs587777794(A;A)
Reference rs587777794(G;G)
Significance Pathogenic
Disease Cowden syndrome 5
Variation info
Gene PIK3CA
CLNDBN Cowden syndrome 5
Reversed 0
HGVS NC_000003.11:g.178922376G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144510.2,