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rs730547

From SNPedia

Orientationminus
Stabilizedminus
Make rs730547(A;A)
Make rs730547(A;G)
Make rs730547(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position34785087
is asnp
is mentioned by
dbSNPrs730547
ebirs730547
HLIrs730547
Exacrs730547
Varsomers730547
Maprs730547
PheGenIrs730547
hapmaprs730547
1000 genomesrs730547
hgdprs730547
ensemblrs730547
gopubmedrs730547
geneviewrs730547
scholarrs730547
googlers730547
pharmgkbrs730547
gwascentralrs730547
openSNPrs730547
23andMers730547
23andMe allrs730547
SNP Nexus

SNPshotrs730547
SNPdbers730547
MSV3drs730547
GWAS Ctlgrs730547
Max Magnitude
? (A;A) (A;G) (G;G) 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 1E-7
Odds Ratio NR NR