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rs16834871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16834871(C;C)
Make rs16834871(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position153023685
is asnp
is mentioned by
dbSNPrs16834871
ebirs16834871
HLIrs16834871
Exacrs16834871
Varsomers16834871
Maprs16834871
PheGenIrs16834871
hapmaprs16834871
1000 genomesrs16834871
hgdprs16834871
ensemblrs16834871
gopubmedrs16834871
geneviewrs16834871
scholarrs16834871
googlers16834871
pharmgkbrs16834871
gwascentralrs16834871
openSNPrs16834871
23andMers16834871
23andMe allrs16834871
SNP Nexus

SNPshotrs16834871
SNPdbers16834871
MSV3drs16834871
GWAS Ctlgrs16834871
GMAF0.1556
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 19706030OA-icon.png] Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking