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rs10495822

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Orientationplus
Stabilizedplus
Make rs10495822(G;G)
Make rs10495822(G;T)
Make rs10495822(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position34447854
is asnp
is mentioned by
dbSNPrs10495822
ebirs10495822
HLIrs10495822
Exacrs10495822
Varsomers10495822
Maprs10495822
PheGenIrs10495822
hapmaprs10495822
1000 genomesrs10495822
hgdprs10495822
ensemblrs10495822
gopubmedrs10495822
geneviewrs10495822
scholarrs10495822
googlers10495822
pharmgkbrs10495822
gwascentralrs10495822
openSNPrs10495822
23andMers10495822
23andMe allrs10495822
SNP Nexus

SNPshotrs10495822
SNPdbers10495822
MSV3drs10495822
GWAS Ctlgrs10495822
Max Magnitude
? (G;G) (G;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