Rs12680546

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Orientationplus
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Make rs12680546(A;G)
Make rs12680546(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position135859496
is asnp
is mentioned by
dbSNPrs12680546
Exacrs12680546
PheGenIrs12680546
nextbiors12680546
hapmaprs12680546
1000 genomesrs12680546
hgdprs12680546
ensemblrs12680546
gopubmedrs12680546
geneviewrs12680546
scholarrs12680546
googlers12680546
pharmgkbrs12680546
gwascentralrs12680546
openSNPrs12680546
23andMers12680546
23andMe allrs12680546
SNP Nexus

SNPshotrs12680546
SNPdbers12680546
MSV3drs12680546
GMAF0.1671
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs12680546
PubMedID [PMID 17362836]
Condition Amyotrophic lateral sclerosis
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR 1.67
95% CI 1.25-2.00



[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.


[PMID 19740415OA-icon.png] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.


GET Evidence
rs12680546
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary