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rs141178472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs141178472(C;C)
Make rs141178472(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position179234393
GenePIK3CA
is asnp
is mentioned by
dbSNPrs141178472
ebirs141178472
HLIrs141178472
Exacrs141178472
Varsomers141178472
Maprs141178472
PheGenIrs141178472
hapmaprs141178472
1000 genomesrs141178472
hgdprs141178472
ensemblrs141178472
gopubmedrs141178472
geneviewrs141178472
scholarrs141178472
googlers141178472
pharmgkbrs141178472
gwascentralrs141178472
openSNPrs141178472
23andMers141178472
23andMe allrs141178472
SNP Nexus

SNPshotrs141178472
SNPdbers141178472
MSV3drs141178472
GWAS Ctlgrs141178472
Max Magnitude0

[PMID 25834816OA-icon.png] A Functional Variant at miR-520a Binding Site in PIK3CA Alters Susceptibility to Colorectal Cancer in a Chinese Han Population

ClinVar
Risk rs141178472(C;C)
Alt rs141178472(C;C)
Reference rs141178472(T;T)
Significance Non-pathogenic
Disease Cowden syndrome
Variation info
Gene PIK3CA
CLNDBN Cowden syndrome
Reversed 0
HGVS NC_000003.11:g.178952181T>C
CLNSRC
CLNACC RCV000235680.1,