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rs4128705

From SNPedia

Orientationplus
Stabilizedplus
Make rs4128705(G;G)
Make rs4128705(G;T)
Make rs4128705(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position91362620
GeneCCSER1
is asnp
is mentioned by
dbSNPrs4128705
ebirs4128705
HLIrs4128705
Exacrs4128705
Varsomers4128705
Maprs4128705
PheGenIrs4128705
hapmaprs4128705
1000 genomesrs4128705
hgdprs4128705
ensemblrs4128705
gopubmedrs4128705
geneviewrs4128705
scholarrs4128705
googlers4128705
pharmgkbrs4128705
gwascentralrs4128705
openSNPrs4128705
23andMers4128705
23andMe allrs4128705
SNP Nexus

SNPshotrs4128705
SNPdbers4128705
MSV3drs4128705
GWAS Ctlgrs4128705
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 6E-6
Odds Ratio NR NR