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

rs4733616

From SNPedia

Orientationplus
Stabilizedplus
Make rs4733616(C;C)
Make rs4733616(C;T)
Make rs4733616(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127649850
is asnp
is mentioned by
dbSNPrs4733616
ebirs4733616
HLIrs4733616
Exacrs4733616
Varsomers4733616
Maprs4733616
PheGenIrs4733616
hapmaprs4733616
1000 genomesrs4733616
hgdprs4733616
ensemblrs4733616
gopubmedrs4733616
geneviewrs4733616
scholarrs4733616
googlers4733616
pharmgkbrs4733616
gwascentralrs4733616
openSNPrs4733616
23andMers4733616
23andMe allrs4733616
SNP Nexus

SNPshotrs4733616
SNPdbers4733616
MSV3drs4733616
GWAS Ctlgrs4733616
GMAF0.1524
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22275265OA-icon.png] Common genetic variants in the 8q24 region and risk of papillary thyroid cancer


[PMID 25939847] Association of common variants on chromosome 8q24 with gastric cancer in Venezuelan patients