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rs16975050

From SNPedia

Orientationplus
Stabilizedplus
Make rs16975050(G;G)
Make rs16975050(G;T)
Make rs16975050(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position41607206
is asnp
is mentioned by
dbSNPrs16975050
ebirs16975050
HLIrs16975050
Exacrs16975050
Varsomers16975050
Maprs16975050
PheGenIrs16975050
hapmaprs16975050
1000 genomesrs16975050
hgdprs16975050
ensemblrs16975050
gopubmedrs16975050
geneviewrs16975050
scholarrs16975050
googlers16975050
pharmgkbrs16975050
gwascentralrs16975050
openSNPrs16975050
23andMers16975050
23andMe allrs16975050
SNP Nexus

SNPshotrs16975050
SNPdbers16975050
MSV3drs16975050
GWAS Ctlgrs16975050
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 5E-7
Odds Ratio NR NR