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rs1047964

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs1047964(C;G)
Make rs1047964(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position117286177
GeneBACE1, RNF214
is asnp
is mentioned by
dbSNPrs1047964
ebirs1047964
HLIrs1047964
Exacrs1047964
Varsomers1047964
Maprs1047964
PheGenIrs1047964
hapmaprs1047964
1000 genomesrs1047964
hgdprs1047964
ensemblrs1047964
gopubmedrs1047964
geneviewrs1047964
scholarrs1047964
googlers1047964
pharmgkbrs1047964
gwascentralrs1047964
openSNPrs1047964
23andMers1047964
23andMe allrs1047964
SNP Nexus

SNPshotrs1047964
SNPdbers1047964
MSV3drs1047964
GWAS Ctlgrs1047964
GMAF0.0427
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21779381OA-icon.png]
Trait
Title Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.
Risk Allele
P-val 8E-7
Odds Ratio 4.6700 [2.53-8.62]