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rs6851442

From SNPedia

Orientationplus
Stabilizedplus
Make rs6851442(A;A)
Make rs6851442(A;G)
Make rs6851442(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position108038126
is asnp
is mentioned by
dbSNPrs6851442
ebirs6851442
HLIrs6851442
Exacrs6851442
Varsomers6851442
Maprs6851442
PheGenIrs6851442
hapmaprs6851442
1000 genomesrs6851442
hgdprs6851442
ensemblrs6851442
gopubmedrs6851442
geneviewrs6851442
scholarrs6851442
googlers6851442
pharmgkbrs6851442
gwascentralrs6851442
openSNPrs6851442
23andMers6851442
23andMe allrs6851442
SNP Nexus

SNPshotrs6851442
SNPdbers6851442
MSV3drs6851442
GWAS Ctlgrs6851442
Max Magnitude
? (A;A) (A;G) (G;G) 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