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rs16902328

From SNPedia

Orientationplus
Stabilizedplus
Make rs16902328(G;G)
Make rs16902328(G;T)
Make rs16902328(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position127701628
GeneCASC11
is asnp
is mentioned by
dbSNPrs16902328
ebirs16902328
HLIrs16902328
Exacrs16902328
Varsomers16902328
Maprs16902328
PheGenIrs16902328
hapmaprs16902328
1000 genomesrs16902328
hgdprs16902328
ensemblrs16902328
gopubmedrs16902328
geneviewrs16902328
scholarrs16902328
googlers16902328
pharmgkbrs16902328
gwascentralrs16902328
openSNPrs16902328
23andMers16902328
23andMe allrs16902328
SNP Nexus

SNPshotrs16902328
SNPdbers16902328
MSV3drs16902328
GWAS Ctlgrs16902328
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 3E-6
Odds Ratio NR NR