rs2431238
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2431238(C;C) |
Make rs2431238(C;T) |
Make rs2431238(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112788672 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs2431238 |
dbSNP (classic) | rs2431238 |
ClinGen | rs2431238 |
ebi | rs2431238 |
HLI | rs2431238 |
Exac | rs2431238 |
Gnomad | rs2431238 |
Varsome | rs2431238 |
LitVar | rs2431238 |
Map | rs2431238 |
PheGenI | rs2431238 |
Biobank | rs2431238 |
1000 genomes | rs2431238 |
hgdp | rs2431238 |
ensembl | rs2431238 |
geneview | rs2431238 |
scholar | rs2431238 |
rs2431238 | |
pharmgkb | rs2431238 |
gwascentral | rs2431238 |
openSNP | rs2431238 |
23andMe | rs2431238 |
SNPshot | rs2431238 |
SNPdbe | rs2431238 |
MSV3d | rs2431238 |
GWAS Ctlg | rs2431238 |
GMAF | 0.258 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20056645] Association of mitotic regulation pathway polymorphisms with pancreatic cancer risk and outcome
ClinVar | |
---|---|
Risk | rs2431238(C;C) |
Alt | rs2431238(C;C) |
Reference | rs2431238(T;T) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000005.9:g.112124369T>C |
CLNSRC | ClinVar |
CLNACC | RCV000073969.1, |
[PMID 18708403] Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.
[PMID 19777185] Association analysis of Wnt pathway genes on prostate-specific antigen recurrence after radical prostatectomy.