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rs3853444

From SNPedia

Orientationminus
Stabilizedminus
Make rs3853444(A;A)
Make rs3853444(A;G)
Make rs3853444(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position110812980
is asnp
is mentioned by
dbSNPrs3853444
ebirs3853444
HLIrs3853444
Exacrs3853444
Varsomers3853444
Maprs3853444
PheGenIrs3853444
hapmaprs3853444
1000 genomesrs3853444
hgdprs3853444
ensemblrs3853444
gopubmedrs3853444
geneviewrs3853444
scholarrs3853444
googlers3853444
pharmgkbrs3853444
gwascentralrs3853444
openSNPrs3853444
23andMers3853444
23andMe allrs3853444
SNP Nexus

SNPshotrs3853444
SNPdbers3853444
MSV3drs3853444
GWAS Ctlgrs3853444
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24778558OA-icon.png]
Trait Coronary heart disease
Title RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families.
Risk Allele G
P-val 5E-6
Odds Ratio 7.69 [2.70-20.0]