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rs1559473

From SNPedia

Orientationplus
Stabilizedplus
Make rs1559473(G;G)
Make rs1559473(G;T)
Make rs1559473(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position222016799
is asnp
is mentioned by
dbSNPrs1559473
ebirs1559473
HLIrs1559473
Exacrs1559473
Varsomers1559473
Maprs1559473
PheGenIrs1559473
hapmaprs1559473
1000 genomesrs1559473
hgdprs1559473
ensemblrs1559473
gopubmedrs1559473
geneviewrs1559473
scholarrs1559473
googlers1559473
pharmgkbrs1559473
gwascentralrs1559473
openSNPrs1559473
23andMers1559473
23andMe allrs1559473
SNP Nexus

SNPshotrs1559473
SNPdbers1559473
MSV3drs1559473
GWAS Ctlgrs1559473
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 1E-6
Odds Ratio NR NR