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rs16938145

From SNPedia

Orientationplus
Stabilizedplus
Make rs16938145(C;C)
Make rs16938145(C;T)
Make rs16938145(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position2256092
is asnp
is mentioned by
dbSNPrs16938145
ebirs16938145
HLIrs16938145
Exacrs16938145
Varsomers16938145
Maprs16938145
PheGenIrs16938145
hapmaprs16938145
1000 genomesrs16938145
hgdprs16938145
ensemblrs16938145
gopubmedrs16938145
geneviewrs16938145
scholarrs16938145
googlers16938145
pharmgkbrs16938145
gwascentralrs16938145
openSNPrs16938145
23andMers16938145
23andMe allrs16938145
SNP Nexus

SNPshotrs16938145
SNPdbers16938145
MSV3drs16938145
GWAS Ctlgrs16938145
Max Magnitude
? (C;C) (C;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 1E-6
Odds Ratio NR NR