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rs17608902

From SNPedia

Orientationplus
Stabilizedplus
Make rs17608902(A;A)
Make rs17608902(A;C)
Make rs17608902(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position128380874
GeneFBN2
is asnp
is mentioned by
dbSNPrs17608902
ebirs17608902
HLIrs17608902
Exacrs17608902
Varsomers17608902
Maprs17608902
PheGenIrs17608902
hapmaprs17608902
1000 genomesrs17608902
hgdprs17608902
ensemblrs17608902
gopubmedrs17608902
geneviewrs17608902
scholarrs17608902
googlers17608902
pharmgkbrs17608902
gwascentralrs17608902
openSNPrs17608902
23andMers17608902
23andMe allrs17608902
SNP Nexus

SNPshotrs17608902
SNPdbers17608902
MSV3drs17608902
GWAS Ctlgrs17608902
GMAF0.05693
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine - clinic-based
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele A
P-val 1E-7
Odds Ratio 1.25 [1.15-1.35]