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

rs16888728

From SNPedia

Orientationplus
Make rs16888728(C;C)
Make rs16888728(C;T)
Make rs16888728(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position116771736
GeneUTP23
is asnp
is mentioned by
dbSNPrs16888728
ebirs16888728
HLIrs16888728
Exacrs16888728
Varsomers16888728
Maprs16888728
PheGenIrs16888728
hapmaprs16888728
1000 genomesrs16888728
hgdprs16888728
ensemblrs16888728
gopubmedrs16888728
geneviewrs16888728
scholarrs16888728
googlers16888728
pharmgkbrs16888728
gwascentralrs16888728
openSNPrs16888728
23andMers16888728
23andMe allrs16888728
SNP Nexus

SNPshotrs16888728
SNPdbers16888728
MSV3drs16888728
GWAS Ctlgrs16888728
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26553438OA-icon.png] Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer