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rs17458018

From SNPedia

Orientationplus
Stabilizedplus
Make rs17458018(C;C)
Make rs17458018(C;T)
Make rs17458018(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position215420652
GeneFN1
is asnp
is mentioned by
dbSNPrs17458018
ebirs17458018
HLIrs17458018
Exacrs17458018
Varsomers17458018
Maprs17458018
PheGenIrs17458018
hapmaprs17458018
1000 genomesrs17458018
hgdprs17458018
ensemblrs17458018
gopubmedrs17458018
geneviewrs17458018
scholarrs17458018
googlers17458018
pharmgkbrs17458018
gwascentralrs17458018
openSNPrs17458018
23andMers17458018
23andMe allrs17458018
SNP Nexus

SNPshotrs17458018
SNPdbers17458018
MSV3drs17458018
GWAS Ctlgrs17458018
GMAF0.03352
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22319020OA-icon.png]
Trait
Title A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
Risk Allele
P-val 0.000007
Odds Ratio 1.2200 None