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rs10489764

From SNPedia

Orientationplus
Stabilizedplus
Make rs10489764(C;C)
Make rs10489764(C;T)
Make rs10489764(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position188116702
is asnp
is mentioned by
dbSNPrs10489764
ebirs10489764
HLIrs10489764
Exacrs10489764
Varsomers10489764
Maprs10489764
PheGenIrs10489764
hapmaprs10489764
1000 genomesrs10489764
hgdprs10489764
ensemblrs10489764
gopubmedrs10489764
geneviewrs10489764
scholarrs10489764
googlers10489764
pharmgkbrs10489764
gwascentralrs10489764
openSNPrs10489764
23andMers10489764
23andMe allrs10489764
SNP Nexus

SNPshotrs10489764
SNPdbers10489764
MSV3drs10489764
GWAS Ctlgrs10489764
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 8E-6
Odds Ratio NR NR