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rs1406961

From SNPedia

Orientationplus
Stabilizedplus
Make rs1406961(A;A)
Make rs1406961(A;C)
Make rs1406961(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position63264568
is asnp
is mentioned by
dbSNPrs1406961
dbSNP (classic)rs1406961
ClinGenrs1406961
ebirs1406961
HLIrs1406961
Exacrs1406961
Gnomadrs1406961
Varsomers1406961
LitVarrs1406961
Maprs1406961
PheGenIrs1406961
Biobankrs1406961
1000 genomesrs1406961
hgdprs1406961
ensemblrs1406961
geneviewrs1406961
scholarrs1406961
googlers1406961
pharmgkbrs1406961
gwascentralrs1406961
openSNPrs1406961
23andMers1406961
SNPshotrs1406961
SNPdbers1406961
MSV3drs1406961
GWAS Ctlgrs1406961
GMAF0.1267
Max Magnitude0
? (A;A) (A;C) (C;C) 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 5E-7
Odds Ratio 12.3300 [4.62-32.87]


[PMID 18661515OA-icon.png] The eukaryotic translation elongation factor eEF1A2 induces neoplastic properties and mediates tumorigenic effects of ZNF217 in precursor cells of human ovarian carcinomas.