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rs10508264

From SNPedia

Orientationplus
Stabilizedplus
Make rs10508264(A;A)
Make rs10508264(A;G)
Make rs10508264(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position3762065
is asnp
is mentioned by
dbSNPrs10508264
ebirs10508264
HLIrs10508264
Exacrs10508264
Varsomers10508264
Maprs10508264
PheGenIrs10508264
hapmaprs10508264
1000 genomesrs10508264
hgdprs10508264
ensemblrs10508264
gopubmedrs10508264
geneviewrs10508264
scholarrs10508264
googlers10508264
pharmgkbrs10508264
gwascentralrs10508264
openSNPrs10508264
23andMers10508264
23andMe allrs10508264
SNP Nexus

SNPshotrs10508264
SNPdbers10508264
MSV3drs10508264
GWAS Ctlgrs10508264
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 2E-6
Odds Ratio NR NR