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rs11987758

From SNPedia

Orientationplus
Stabilizedplus
Make rs11987758(A;A)
Make rs11987758(A;G)
Make rs11987758(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position2180583
is asnp
is mentioned by
dbSNPrs11987758
ebirs11987758
HLIrs11987758
Exacrs11987758
Varsomers11987758
Maprs11987758
PheGenIrs11987758
hapmaprs11987758
1000 genomesrs11987758
hgdprs11987758
ensemblrs11987758
gopubmedrs11987758
geneviewrs11987758
scholarrs11987758
googlers11987758
pharmgkbrs11987758
gwascentralrs11987758
openSNPrs11987758
23andMers11987758
23andMe allrs11987758
SNP Nexus

SNPshotrs11987758
SNPdbers11987758
MSV3drs11987758
GWAS Ctlgrs11987758
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 8E-7
Odds Ratio NR NR