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rs10501765

From SNPedia

Orientationplus
Stabilizedplus
Make rs10501765(C;C)
Make rs10501765(C;T)
Make rs10501765(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position91924110
is asnp
is mentioned by
dbSNPrs10501765
ebirs10501765
HLIrs10501765
Exacrs10501765
Varsomers10501765
Maprs10501765
PheGenIrs10501765
hapmaprs10501765
1000 genomesrs10501765
hgdprs10501765
ensemblrs10501765
gopubmedrs10501765
geneviewrs10501765
scholarrs10501765
googlers10501765
pharmgkbrs10501765
gwascentralrs10501765
openSNPrs10501765
23andMers10501765
23andMe allrs10501765
SNP Nexus

SNPshotrs10501765
SNPdbers10501765
MSV3drs10501765
GWAS Ctlgrs10501765
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