rs11954856
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11954856(G;G) |
Make rs11954856(G;T) |
Make rs11954856(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112751630 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs11954856 |
dbSNP (classic) | rs11954856 |
ClinGen | rs11954856 |
ebi | rs11954856 |
HLI | rs11954856 |
Exac | rs11954856 |
Gnomad | rs11954856 |
Varsome | rs11954856 |
LitVar | rs11954856 |
Map | rs11954856 |
PheGenI | rs11954856 |
Biobank | rs11954856 |
1000 genomes | rs11954856 |
hgdp | rs11954856 |
ensembl | rs11954856 |
geneview | rs11954856 |
scholar | rs11954856 |
rs11954856 | |
pharmgkb | rs11954856 |
gwascentral | rs11954856 |
openSNP | rs11954856 |
23andMe | rs11954856 |
SNPshot | rs11954856 |
SNPdbe | rs11954856 |
MSV3d | rs11954856 |
GWAS Ctlg | rs11954856 |
GMAF | 0.3898 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 24078348] An Analysis of Polymorphisms Within the Wnt Signaling Pathway in Relation to Ovarian Cancer Risk in a Polish Population
[PMID 18708403] Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.
ClinVar | |
---|---|
Risk | rs11954856(G;G) |
Alt | rs11954856(G;G) |
Reference | rs11954856(T;T) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000005.9:g.112087327T>G |
CLNSRC | ClinVar |
CLNACC | RCV000073790.1, |