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rs982274

From SNPedia

Orientationplus
Stabilizedplus
Make rs982274(G;G)
Make rs982274(G;T)
Make rs982274(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position18107413
GeneCHODL
is asnp
is mentioned by
dbSNPrs982274
ebirs982274
HLIrs982274
Exacrs982274
Varsomers982274
Maprs982274
PheGenIrs982274
hapmaprs982274
1000 genomesrs982274
hgdprs982274
ensemblrs982274
gopubmedrs982274
geneviewrs982274
scholarrs982274
googlers982274
pharmgkbrs982274
gwascentralrs982274
openSNPrs982274
23andMers982274
23andMe allrs982274
SNP Nexus

SNPshotrs982274
SNPdbers982274
MSV3drs982274
GWAS Ctlgrs982274
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 6E-6
Odds Ratio NR NR