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rs1464443

From SNPedia

Orientationplus
Stabilizedplus
Make rs1464443(A;A)
Make rs1464443(A;C)
Make rs1464443(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position212050001
GeneERBB4
is asnp
is mentioned by
dbSNPrs1464443
ebirs1464443
HLIrs1464443
Exacrs1464443
Varsomers1464443
Maprs1464443
PheGenIrs1464443
hapmaprs1464443
1000 genomesrs1464443
hgdprs1464443
ensemblrs1464443
gopubmedrs1464443
geneviewrs1464443
scholarrs1464443
googlers1464443
pharmgkbrs1464443
gwascentralrs1464443
openSNPrs1464443
23andMers1464443
23andMe allrs1464443
SNP Nexus

SNPshotrs1464443
SNPdbers1464443
MSV3drs1464443
GWAS Ctlgrs1464443
Max Magnitude
? (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 1E-6
Odds Ratio NR NR