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rs12891047

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
Make rs12891047(A;C)
Make rs12891047(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position67776358
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs12891047
dbSNP (old)rs12891047
ClinGenrs12891047
ebirs12891047
HLIrs12891047
Exacrs12891047
Gnomadrs12891047
Varsomers12891047
Maprs12891047
PheGenIrs12891047
Biobankrs12891047
1000 genomesrs12891047
hgdprs12891047
ensemblrs12891047
gopubmedrs12891047
geneviewrs12891047
scholarrs12891047
googlers12891047
pharmgkbrs12891047
gwascentralrs12891047
openSNPrs12891047
23andMers12891047
23andMe allrs12891047
SNPshotrs12891047
SNPdbers12891047
MSV3drs12891047
GWAS Ctlgrs12891047
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 6E-7
Odds Ratio NR NR