Rs3825776

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is asnp
is mentioned by
dbSNPrs3825776
hapmaprs3825776
hgdprs3825776
ensemblrs3825776
gopubmedrs3825776
scholarrs3825776
googlers3825776
pharmgkbrs3825776
hgvbaseg2prs3825776
medrefsnprs3825776
23andMers3825776
SNP Nexus

GeneLIPC
Chromosome15
Orientationminus
Position56534121
GenotypeEffect
rs3825776(A;A)average
rs3825776(A;G)1.3x risk for ALS
rs3825776(G;G)>1.3x risk for ALS


Genotypes Magnitude Summary
Rs3825776(A;A) 00 average
Rs3825776(A;G) 1.3x risk for ALS
Rs3825776(G;G) >1.3x risk for ALS
Rs3825776(T;T) 00
rs3825776, a SNP in the region of the LIPC gene on chromosome 15, has been associated with the sporadic form of ALS (Lou Gehrig's disease) in a study of 1000+ European patients. The odds ratio for the risk allele rs3825776(G) is 1.34 (CI: 1.12 - 1.46). [PMID 18084291]
? (A;A) (A;G) (G;G)
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