rs7013278
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7013278(C;C) |
Make rs7013278(C;T) |
Make rs7013278(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 127402647 |
Gene | CASC8, CCAT2 |
is a | snp |
is | mentioned by |
dbSNP | rs7013278 |
dbSNP (classic) | rs7013278 |
ClinGen | rs7013278 |
ebi | rs7013278 |
HLI | rs7013278 |
Exac | rs7013278 |
Gnomad | rs7013278 |
Varsome | rs7013278 |
LitVar | rs7013278 |
Map | rs7013278 |
PheGenI | rs7013278 |
Biobank | rs7013278 |
1000 genomes | rs7013278 |
hgdp | rs7013278 |
ensembl | rs7013278 |
geneview | rs7013278 |
scholar | rs7013278 |
rs7013278 | |
pharmgkb | rs7013278 |
gwascentral | rs7013278 |
openSNP | rs7013278 |
23andMe | rs7013278 |
SNPshot | rs7013278 |
SNPdbe | rs7013278 |
MSV3d | rs7013278 |
GWAS Ctlg | rs7013278 |
GMAF | 0.3682 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 17618282] A common genetic risk factor for colorectal and prostate cancer.
[PMID 18704501] Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers.
[PMID 19155440] Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21.
[PMID 19528667] Association of chromosome 8q variants with prostate cancer risk in Caucasian and Hispanic men.
[PMID 22848671] Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.