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rs10145110

From SNPedia

Orientationplus
Stabilizedplus
Make rs10145110(C;C)
Make rs10145110(C;T)
Make rs10145110(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position101008533
is asnp
is mentioned by
dbSNPrs10145110
ebirs10145110
HLIrs10145110
Exacrs10145110
Varsomers10145110
Maprs10145110
PheGenIrs10145110
hapmaprs10145110
1000 genomesrs10145110
hgdprs10145110
ensemblrs10145110
gopubmedrs10145110
geneviewrs10145110
scholarrs10145110
googlers10145110
pharmgkbrs10145110
gwascentralrs10145110
openSNPrs10145110
23andMers10145110
23andMe allrs10145110
SNP Nexus

SNPshotrs10145110
SNPdbers10145110
MSV3drs10145110
GWAS Ctlgrs10145110
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 1E-7
Odds Ratio NR NR