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rs17675602

From SNPedia

Orientationplus
Stabilizedplus
Make rs17675602(A;A)
Make rs17675602(A;T)
Make rs17675602(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position82929158
GeneCDH13
is asnp
is mentioned by
dbSNPrs17675602
ebirs17675602
HLIrs17675602
Exacrs17675602
Varsomers17675602
Maprs17675602
PheGenIrs17675602
hapmaprs17675602
1000 genomesrs17675602
hgdprs17675602
ensemblrs17675602
gopubmedrs17675602
geneviewrs17675602
scholarrs17675602
googlers17675602
pharmgkbrs17675602
gwascentralrs17675602
openSNPrs17675602
23andMers17675602
23andMe allrs17675602
SNP Nexus

SNPshotrs17675602
SNPdbers17675602
MSV3drs17675602
GWAS Ctlgrs17675602
GMAF0.06428
Max Magnitude
? (A;A) (A;T) (T;T) 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 T
P-val 5E-6
Odds Ratio 1.21 [1.12-1.32]