rs10487132
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10487132(A;A) |
| Make rs10487132(A;G) |
| Make rs10487132(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 95390993 |
| Gene | PON3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10487132 |
| dbSNP (classic) | rs10487132 |
| ClinGen | rs10487132 |
| ebi | rs10487132 |
| HLI | rs10487132 |
| Exac | rs10487132 |
| Gnomad | rs10487132 |
| Varsome | rs10487132 |
| LitVar | rs10487132 |
| Map | rs10487132 |
| PheGenI | rs10487132 |
| Biobank | rs10487132 |
| 1000 genomes | rs10487132 |
| hgdp | rs10487132 |
| ensembl | rs10487132 |
| geneview | rs10487132 |
| scholar | rs10487132 |
| rs10487132 | |
| pharmgkb | rs10487132 |
| gwascentral | rs10487132 |
| openSNP | rs10487132 |
| 23andMe | rs10487132 |
| SNPshot | rs10487132 |
| SNPdbe | rs10487132 |
| MSV3d | rs10487132 |
| GWAS Ctlg | rs10487132 |
| GMAF | 0.1956 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 19321847
] 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 17702780] Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.
[PMID 18618303] 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.
