rs141178472
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs141178472(C;C) |
Make rs141178472(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 179234393 |
Gene | PIK3CA |
is a | snp |
is | mentioned by |
dbSNP | rs141178472 |
dbSNP (classic) | rs141178472 |
ClinGen | rs141178472 |
ebi | rs141178472 |
HLI | rs141178472 |
Exac | rs141178472 |
Gnomad | rs141178472 |
Varsome | rs141178472 |
LitVar | rs141178472 |
Map | rs141178472 |
PheGenI | rs141178472 |
Biobank | rs141178472 |
1000 genomes | rs141178472 |
hgdp | rs141178472 |
ensembl | rs141178472 |
geneview | rs141178472 |
scholar | rs141178472 |
rs141178472 | |
pharmgkb | rs141178472 |
gwascentral | rs141178472 |
openSNP | rs141178472 |
23andMe | rs141178472 |
SNPshot | rs141178472 |
SNPdbe | rs141178472 |
MSV3d | rs141178472 |
GWAS Ctlg | rs141178472 |
Max Magnitude | 0 |
[PMID 25834816] 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, |