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rs4482178

From SNPedia

Orientationplus
Stabilizedplus
Make rs4482178(A;A)
Make rs4482178(A;C)
Make rs4482178(C;C)
ReferenceGRCh38 38.1/142
Chromosome13
Position85529954
GeneLINC00351
is asnp
is mentioned by
dbSNPrs4482178
ebirs4482178
HLIrs4482178
Exacrs4482178
Varsomers4482178
Maprs4482178
PheGenIrs4482178
hapmaprs4482178
1000 genomesrs4482178
hgdprs4482178
ensemblrs4482178
gopubmedrs4482178
geneviewrs4482178
scholarrs4482178
googlers4482178
pharmgkbrs4482178
gwascentralrs4482178
openSNPrs4482178
23andMers4482178
23andMe allrs4482178
SNP Nexus

SNPshotrs4482178
SNPdbers4482178
MSV3drs4482178
GWAS Ctlgrs4482178
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-7
Odds Ratio NR NR