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rs4148112

From SNPedia

Orientationplus
Stabilizedplus
Make rs4148112(C;C)
Make rs4148112(C;T)
Make rs4148112(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position42230666
GeneABCG1
is asnp
is mentioned by
dbSNPrs4148112
ebirs4148112
HLIrs4148112
Exacrs4148112
Varsomers4148112
Maprs4148112
PheGenIrs4148112
hapmaprs4148112
1000 genomesrs4148112
hgdprs4148112
ensemblrs4148112
gopubmedrs4148112
geneviewrs4148112
scholarrs4148112
googlers4148112
pharmgkbrs4148112
gwascentralrs4148112
openSNPrs4148112
23andMers4148112
23andMe allrs4148112
SNP Nexus

SNPshotrs4148112
SNPdbers4148112
MSV3drs4148112
GWAS Ctlgrs4148112
Max Magnitude
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