Have questions? Visit https://www.reddit.com/r/SNPedia

rs10808555

From SNPedia
Orientationplus
Stabilizedplus
Make rs10808555(A;A)
Make rs10808555(A;G)
Make rs10808555(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position127397266
GeneCASC8
is asnp
is mentioned by
dbSNPrs10808555
dbSNP (old)rs10808555
ClinGenrs10808555
ebirs10808555
HLIrs10808555
Exacrs10808555
Gnomadrs10808555
Varsomers10808555
Maprs10808555
PheGenIrs10808555
Biobankrs10808555
1000 genomesrs10808555
hgdprs10808555
ensemblrs10808555
gopubmedrs10808555
geneviewrs10808555
scholarrs10808555
googlers10808555
pharmgkbrs10808555
gwascentralrs10808555
openSNPrs10808555
23andMers10808555
23andMe allrs10808555
SNPshotrs10808555
SNPdbers10808555
MSV3drs10808555
GWAS Ctlgrs10808555
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 27769063OA-icon.png] Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.