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rs7013278

From SNPedia

Orientationplus
Stabilizedplus
Make rs7013278(C;C)
Make rs7013278(C;T)
Make rs7013278(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127402647
GeneCCAT2, LOC101930033
is asnp
is mentioned by
dbSNPrs7013278
ebirs7013278
HLIrs7013278
Exacrs7013278
Varsomers7013278
Maprs7013278
PheGenIrs7013278
hapmaprs7013278
1000 genomesrs7013278
hgdprs7013278
ensemblrs7013278
gopubmedrs7013278
geneviewrs7013278
scholarrs7013278
googlers7013278
pharmgkbrs7013278
gwascentralrs7013278
openSNPrs7013278
23andMers7013278
23andMe allrs7013278
SNP Nexus

SNPshotrs7013278
SNPdbers7013278
MSV3drs7013278
GWAS Ctlgrs7013278
GMAF0.3682
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 19155440OA-icon.png] Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21.


[PMID 19528667OA-icon.png] Association of chromosome 8q variants with prostate cancer risk in Caucasian and Hispanic men.


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