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rs1572511

From SNPedia

Orientationplus
Stabilizedplus
Make rs1572511(C;C)
Make rs1572511(C;T)
Make rs1572511(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position177652066
is asnp
is mentioned by
dbSNPrs1572511
ebirs1572511
HLIrs1572511
Exacrs1572511
Varsomers1572511
Maprs1572511
PheGenIrs1572511
hapmaprs1572511
1000 genomesrs1572511
hgdprs1572511
ensemblrs1572511
gopubmedrs1572511
geneviewrs1572511
scholarrs1572511
googlers1572511
pharmgkbrs1572511
gwascentralrs1572511
openSNPrs1572511
23andMers1572511
23andMe allrs1572511
SNP Nexus

SNPshotrs1572511
SNPdbers1572511
MSV3drs1572511
GWAS Ctlgrs1572511
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 3E-6
Odds Ratio NR NR