rs6774494

Orientation

plus

Stabilized

plus

Make rs6774494(A;A)

Make rs6774494(A;G)

Make rs6774494(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

169364845

Gene

MECOM

is a	snp
is	mentioned by
dbSNP	rs6774494
dbSNP (classic)	rs6774494
ClinGen	rs6774494
ebi	rs6774494
HLI	rs6774494
Exac	rs6774494
Gnomad	rs6774494
Varsome	rs6774494
LitVar	rs6774494
Map	rs6774494
PheGenI	rs6774494
Biobank	rs6774494
1000 genomes	rs6774494
hgdp	rs6774494
ensembl	rs6774494
geneview	rs6774494
scholar	rs6774494
google	rs6774494
pharmgkb	rs6774494
gwascentral	rs6774494
openSNP	rs6774494
23andMe	rs6774494
SNPshot	rs6774494
SNPdbe	rs6774494
MSV3d	rs6774494
GWAS Ctlg	rs6774494

GMAF

0.4862

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

GWAS snp
PMID	[PMID 20512145]
Trait	Nasopharyngeal carcinoma
Title	A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
Risk Allele
P-val	1E-8
Odds Ratio	1.19 [1.12-1.27]

OMIM	607107
Desc
Variant
Related	also

[PMID 27517745] Nasopharyngeal carcinoma risk prediction via salivary detection of host and Epstein-Barr virus genetic variants.

[PMID 28467961] Detection of nasopharyngeal carcinoma susceptibility with single nucleotide polymorphism analysis using next-generation sequencing technology.

[PMID 28881764 ] Detection of nasopharyngeal carcinoma susceptibility with single nucleotide polymorphism analysis using next-generation sequencing technology.