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rs7999075

From SNPedia

Orientationplus
Stabilizedplus
Make rs7999075(A;A)
Make rs7999075(A;C)
Make rs7999075(C;C)
ReferenceGRCh38 38.1/142
Chromosome13
Position22046068
is asnp
is mentioned by
dbSNPrs7999075
ebirs7999075
HLIrs7999075
Exacrs7999075
Varsomers7999075
Maprs7999075
PheGenIrs7999075
hapmaprs7999075
1000 genomesrs7999075
hgdprs7999075
ensemblrs7999075
gopubmedrs7999075
geneviewrs7999075
scholarrs7999075
googlers7999075
pharmgkbrs7999075
gwascentralrs7999075
openSNPrs7999075
23andMers7999075
23andMe allrs7999075
SNP Nexus

SNPshotrs7999075
SNPdbers7999075
MSV3drs7999075
GWAS Ctlgrs7999075
Max Magnitude
? (A;A) (A;C) (C;C) 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-6
Odds Ratio NR NR