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rs6531209

From SNPedia

Orientationplus
Stabilizedplus
Make rs6531209(G;G)
Make rs6531209(G;T)
Make rs6531209(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position20134962
is asnp
is mentioned by
dbSNPrs6531209
ebirs6531209
HLIrs6531209
Exacrs6531209
Varsomers6531209
Maprs6531209
PheGenIrs6531209
hapmaprs6531209
1000 genomesrs6531209
hgdprs6531209
ensemblrs6531209
gopubmedrs6531209
geneviewrs6531209
scholarrs6531209
googlers6531209
pharmgkbrs6531209
gwascentralrs6531209
openSNPrs6531209
23andMers6531209
23andMe allrs6531209
SNP Nexus

SNPshotrs6531209
SNPdbers6531209
MSV3drs6531209
GWAS Ctlgrs6531209
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 3E-6
Odds Ratio NR NR