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rs3776467

From SNPedia

Orientationminus
Stabilizedminus
Make rs3776467(C;C)
Make rs3776467(C;T)
Make rs3776467(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position7876202
GeneMTRR
is asnp
is mentioned by
dbSNPrs3776467
dbSNP (classic)rs3776467
ClinGenrs3776467
ebirs3776467
HLIrs3776467
Exacrs3776467
Gnomadrs3776467
Varsomers3776467
LitVarrs3776467
Maprs3776467
PheGenIrs3776467
Biobankrs3776467
1000 genomesrs3776467
hgdprs3776467
ensemblrs3776467
geneviewrs3776467
scholarrs3776467
googlers3776467
pharmgkbrs3776467
gwascentralrs3776467
openSNPrs3776467
23andMers3776467
SNPshotrs3776467
SNPdbers3776467
MSV3drs3776467
GWAS Ctlgrs3776467
GMAF0.4541
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22665368OA-icon.png] Sex-specific association of sequence variants in CBS and MTRR with risk for promoter hypermethylation in the lung epithelium of smokers