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

rs12218935

From SNPedia

Orientationplus
Stabilizedplus
Make rs12218935(C;C)
Make rs12218935(C;T)
Make rs12218935(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position117989592
is asnp
is mentioned by
dbSNPrs12218935
ClinGenrs12218935
ebirs12218935
HLIrs12218935
Exacrs12218935
Varsomers12218935
Maprs12218935
PheGenIrs12218935
hapmaprs12218935
1000 genomesrs12218935
hgdprs12218935
ensemblrs12218935
gopubmedrs12218935
geneviewrs12218935
scholarrs12218935
googlers12218935
pharmgkbrs12218935
gwascentralrs12218935
openSNPrs12218935
23andMers12218935
23andMe allrs12218935
SNP Nexus

SNPshotrs12218935
SNPdbers12218935
MSV3drs12218935
GWAS Ctlgrs12218935
GMAF0.3609
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22318908OA-icon.png] Genetic variants within ultraconserved elements and susceptibility to right- and left-sided colorectal adenocarcinoma