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rs2159222

From SNPedia

Orientationplus
Stabilizedplus
Make rs2159222(A;A)
Make rs2159222(A;T)
Make rs2159222(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position15718375
GeneLOC101927558
is asnp
is mentioned by
dbSNPrs2159222
ebirs2159222
HLIrs2159222
Exacrs2159222
Varsomers2159222
Maprs2159222
PheGenIrs2159222
hapmaprs2159222
1000 genomesrs2159222
hgdprs2159222
ensemblrs2159222
gopubmedrs2159222
geneviewrs2159222
scholarrs2159222
googlers2159222
pharmgkbrs2159222
gwascentralrs2159222
openSNPrs2159222
23andMers2159222
23andMe allrs2159222
SNP Nexus

SNPshotrs2159222
SNPdbers2159222
MSV3drs2159222
GWAS Ctlgrs2159222
GMAF0.191
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine with aura
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 8E-6
Odds Ratio 1.16 [1.09-1.23]