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rs4809847

From SNPedia

Orientationplus
Stabilizedplus
Make rs4809847(G;G)
Make rs4809847(G;T)
Make rs4809847(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position51491782
GeneNFATC2
is asnp
is mentioned by
dbSNPrs4809847
ebirs4809847
HLIrs4809847
Exacrs4809847
Varsomers4809847
Maprs4809847
PheGenIrs4809847
hapmaprs4809847
1000 genomesrs4809847
hgdprs4809847
ensemblrs4809847
gopubmedrs4809847
geneviewrs4809847
scholarrs4809847
googlers4809847
pharmgkbrs4809847
gwascentralrs4809847
openSNPrs4809847
23andMers4809847
23andMe allrs4809847
SNP Nexus

SNPshotrs4809847
SNPdbers4809847
MSV3drs4809847
GWAS Ctlgrs4809847
Max Magnitude
? (G;G) (G;T) (T;T) 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 5E-6
Odds Ratio NR NR