rs4141463
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4141463(C;C) |
| Make rs4141463(C;T) |
| Make rs4141463(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 14766825 |
| Gene | MACROD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4141463 |
| dbSNP (classic) | rs4141463 |
| ClinGen | rs4141463 |
| ebi | rs4141463 |
| HLI | rs4141463 |
| Exac | rs4141463 |
| Gnomad | rs4141463 |
| Varsome | rs4141463 |
| LitVar | rs4141463 |
| Map | rs4141463 |
| PheGenI | rs4141463 |
| Biobank | rs4141463 |
| 1000 genomes | rs4141463 |
| hgdp | rs4141463 |
| ensembl | rs4141463 |
| geneview | rs4141463 |
| scholar | rs4141463 |
| rs4141463 | |
| pharmgkb | rs4141463 |
| gwascentral | rs4141463 |
| openSNP | rs4141463 |
| 23andMe | rs4141463 |
| SNPshot | rs4141463 |
| SNPdbe | rs4141463 |
| MSV3d | rs4141463 |
| GWAS Ctlg | rs4141463 |
| GMAF | 0.3875 |
| Max Magnitude | 0 |
rs4141463 is a SNP within an intron of the MACROD2 gene.
A 2010 study by the Autism Genome Project of 1,558 "rigorously defined" autism spectrum disorder families found some - but slight - evidence for an association between rs4141463 and risk for autism.[PMID 20663923
]
However, an independent case-control study published in 2011 of 1,170 cases of autism spectrum disorder patients failed to replicate any association between autism risk and rs4141463.[PMID 21656903]
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
