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rs2850146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2850146(C;G)
Make rs2850146(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position43080476
is asnp
is mentioned by
dbSNPrs2850146
ebirs2850146
HLIrs2850146
Exacrs2850146
Varsomers2850146
Maprs2850146
PheGenIrs2850146
hapmaprs2850146
1000 genomesrs2850146
hgdprs2850146
ensemblrs2850146
gopubmedrs2850146
geneviewrs2850146
scholarrs2850146
googlers2850146
pharmgkbrs2850146
gwascentralrs2850146
openSNPrs2850146
23andMers2850146
23andMe allrs2850146
SNP Nexus

SNPshotrs2850146
SNPdbers2850146
MSV3drs2850146
GWAS Ctlgrs2850146
GMAF0.06703
Max Magnitude0
? (C;C) (C;G) (G;G) 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