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rs10487132

From SNPedia

Orientationplus
Stabilizedplus
Make rs10487132(A;A)
Make rs10487132(A;G)
Make rs10487132(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position95390993
GenePON3
is asnp
is mentioned by
dbSNPrs10487132
ebirs10487132
HLIrs10487132
Exacrs10487132
Varsomers10487132
Maprs10487132
PheGenIrs10487132
hapmaprs10487132
1000 genomesrs10487132
hgdprs10487132
ensemblrs10487132
gopubmedrs10487132
geneviewrs10487132
scholarrs10487132
googlers10487132
pharmgkbrs10487132
gwascentralrs10487132
openSNPrs10487132
23andMers10487132
23andMe allrs10487132
SNP Nexus

SNPshotrs10487132
SNPdbers10487132
MSV3drs10487132
GWAS Ctlgrs10487132
GMAF0.1956
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19321847OA-icon.png] No association between rs10487132 and amyotrophic lateral sclerosis was seen in this large meta-analysis.


[PMID 16822964] Paraoxonase cluster polymorphisms are associated with sporadic ALS.


[PMID 17702780OA-icon.png] Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.


[PMID 18618303OA-icon.png] A common haplotype within the PON1 promoter region is associated with sporadic ALS.


[PMID 22884547] Association analysis of PON polymorphisms in sporadic ALS in a Chinese population.