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rs6722486

From SNPedia

Orientationplus
Stabilizedplus
Make rs6722486(C;C)
Make rs6722486(C;T)
Make rs6722486(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position208591041
GeneLOC101927960
is asnp
is mentioned by
dbSNPrs6722486
ebirs6722486
HLIrs6722486
Exacrs6722486
Varsomers6722486
Maprs6722486
PheGenIrs6722486
hapmaprs6722486
1000 genomesrs6722486
hgdprs6722486
ensemblrs6722486
gopubmedrs6722486
geneviewrs6722486
scholarrs6722486
googlers6722486
pharmgkbrs6722486
gwascentralrs6722486
openSNPrs6722486
23andMers6722486
23andMe allrs6722486
SNP Nexus

SNPshotrs6722486
SNPdbers6722486
MSV3drs6722486
GWAS Ctlgrs6722486
Max Magnitude
? (C;C) (C;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