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rs10808556

From SNPedia

Orientationplus
Stabilizedplus
Make rs10808556(C;C)
Make rs10808556(C;T)
Make rs10808556(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127400902
GeneCCAT2, LOC101930033
is asnp
is mentioned by
dbSNPrs10808556
ebirs10808556
HLIrs10808556
Exacrs10808556
Varsomers10808556
Maprs10808556
PheGenIrs10808556
hapmaprs10808556
1000 genomesrs10808556
hgdprs10808556
ensemblrs10808556
gopubmedrs10808556
geneviewrs10808556
scholarrs10808556
googlers10808556
pharmgkbrs10808556
gwascentralrs10808556
openSNPrs10808556
23andMers10808556
23andMe allrs10808556
SNP Nexus

SNPshotrs10808556
SNPdbers10808556
MSV3drs10808556
GWAS Ctlgrs10808556
GMAF0.4444
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM611469
DescCOLORECTAL CANCER, SUSCEPTIBILITY TO, 2; CRCS2
Variant
Relatedalso
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[PMID 18704501OA-icon.png] Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers.


[PMID 18973230OA-icon.png] Breast cancer susceptibility alleles and ovarian cancer risk in 2 study populations.


[PMID 19155440OA-icon.png] Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21.


[PMID 19543528OA-icon.png] Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.


[PMID 21455501OA-icon.png] Genetic variants on chromosome 8q24 and colorectal neoplasia risk: a case-control study in China and a meta-analysis of the published literature.


[PMID 22848671OA-icon.png] Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.