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rs3770549

From SNPedia

Orientationplus
Stabilizedplus
Make rs3770549(A;A)
Make rs3770549(A;T)
Make rs3770549(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position215995827
GeneMREG
is asnp
is mentioned by
dbSNPrs3770549
ebirs3770549
HLIrs3770549
Exacrs3770549
Varsomers3770549
Maprs3770549
PheGenIrs3770549
hapmaprs3770549
1000 genomesrs3770549
hgdprs3770549
ensemblrs3770549
gopubmedrs3770549
geneviewrs3770549
scholarrs3770549
googlers3770549
pharmgkbrs3770549
gwascentralrs3770549
openSNPrs3770549
23andMers3770549
23andMe allrs3770549
SNP Nexus

SNPshotrs3770549
SNPdbers3770549
MSV3drs3770549
GWAS Ctlgrs3770549
GMAF0.3365
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Se levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val 3E-6
Odds Ratio .16 [0.092-0.230] unit increase