Have questions? Visit https://www.reddit.com/r/SNPedia

rs6137726

From SNPedia

Orientationplus
Stabilizedplus
Make rs6137726(A;A)
Make rs6137726(A;C)
Make rs6137726(C;C)
ReferenceGRCh38 38.1/142
Chromosome20
Position22691782
is asnp
is mentioned by
dbSNPrs6137726
ebirs6137726
HLIrs6137726
Exacrs6137726
Varsomers6137726
Maprs6137726
PheGenIrs6137726
hapmaprs6137726
1000 genomesrs6137726
hgdprs6137726
ensemblrs6137726
gopubmedrs6137726
geneviewrs6137726
scholarrs6137726
googlers6137726
pharmgkbrs6137726
gwascentralrs6137726
openSNPrs6137726
23andMers6137726
23andMe allrs6137726
SNP Nexus

SNPshotrs6137726
SNPdbers6137726
MSV3drs6137726
GWAS Ctlgrs6137726
Max Magnitude
? (A;A) (A;C) (C;C) 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 9E-7
Odds Ratio NR NR