rs4733616

Orientation

plus

Stabilized

plus

Make rs4733616(C;C)

Make rs4733616(C;T)

Make rs4733616(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

127649850

is a	snp
is	mentioned by
dbSNP	rs4733616
dbSNP (classic)	rs4733616
ClinGen	rs4733616
ebi	rs4733616
HLI	rs4733616
Exac	rs4733616
Gnomad	rs4733616
Varsome	rs4733616
LitVar	rs4733616
Map	rs4733616
PheGenI	rs4733616
Biobank	rs4733616
1000 genomes	rs4733616
hgdp	rs4733616
ensembl	rs4733616
geneview	rs4733616
scholar	rs4733616
google	rs4733616
pharmgkb	rs4733616
gwascentral	rs4733616
openSNP	rs4733616
23andMe	rs4733616
SNPshot	rs4733616
SNPdbe	rs4733616
MSV3d	rs4733616
GWAS Ctlg	rs4733616

GMAF

0.1524

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 22275265] 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