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rs551585

From SNPedia

Orientationminus
Stabilizedminus
Make rs551585(G;G)
Make rs551585(G;T)
Make rs551585(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position76660688
is asnp
is mentioned by
dbSNPrs551585
ebirs551585
HLIrs551585
Exacrs551585
Varsomers551585
Maprs551585
PheGenIrs551585
hapmaprs551585
1000 genomesrs551585
hgdprs551585
ensemblrs551585
gopubmedrs551585
geneviewrs551585
scholarrs551585
googlers551585
pharmgkbrs551585
gwascentralrs551585
openSNPrs551585
23andMers551585
23andMe allrs551585
SNP Nexus

SNPshotrs551585
SNPdbers551585
MSV3drs551585
GWAS Ctlgrs551585
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 3E-7
Odds Ratio NR NR