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rs11062578

From SNPedia

Orientationplus
Stabilizedplus
Make rs11062578(A;A)
Make rs11062578(A;G)
Make rs11062578(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position3218001
GeneTSPAN9
is asnp
is mentioned by
dbSNPrs11062578
ebirs11062578
HLIrs11062578
Exacrs11062578
Varsomers11062578
Maprs11062578
PheGenIrs11062578
hapmaprs11062578
1000 genomesrs11062578
hgdprs11062578
ensemblrs11062578
gopubmedrs11062578
geneviewrs11062578
scholarrs11062578
googlers11062578
pharmgkbrs11062578
gwascentralrs11062578
openSNPrs11062578
23andMers11062578
23andMe allrs11062578
SNP Nexus

SNPshotrs11062578
SNPdbers11062578
MSV3drs11062578
GWAS Ctlgrs11062578
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 3E-6
Odds Ratio NR NR