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rs2685056

From SNPedia

Orientationminus
Stabilizedminus
Make rs2685056(C;C)
Make rs2685056(C;T)
Make rs2685056(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position104699729
is asnp
is mentioned by
dbSNPrs2685056
ebirs2685056
HLIrs2685056
Exacrs2685056
Varsomers2685056
Maprs2685056
PheGenIrs2685056
hapmaprs2685056
1000 genomesrs2685056
hgdprs2685056
ensemblrs2685056
gopubmedrs2685056
geneviewrs2685056
scholarrs2685056
googlers2685056
pharmgkbrs2685056
gwascentralrs2685056
openSNPrs2685056
23andMers2685056
23andMe allrs2685056
SNP Nexus

SNPshotrs2685056
SNPdbers2685056
MSV3drs2685056
GWAS Ctlgrs2685056
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 4E-8
Odds Ratio 2.58 [1.939965-3.434586]