rs7766973
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7766973(C;C) |
| Make rs7766973(C;T) |
| Make rs7766973(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 15267820 |
| Gene | JARID2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7766973 |
| dbSNP (classic) | rs7766973 |
| ClinGen | rs7766973 |
| ebi | rs7766973 |
| HLI | rs7766973 |
| Exac | rs7766973 |
| Gnomad | rs7766973 |
| Varsome | rs7766973 |
| LitVar | rs7766973 |
| Map | rs7766973 |
| PheGenI | rs7766973 |
| Biobank | rs7766973 |
| 1000 genomes | rs7766973 |
| hgdp | rs7766973 |
| ensembl | rs7766973 |
| geneview | rs7766973 |
| scholar | rs7766973 |
| rs7766973 | |
| pharmgkb | rs7766973 |
| gwascentral | rs7766973 |
| openSNP | rs7766973 |
| 23andMe | rs7766973 |
| SNPshot | rs7766973 |
| SNPdbe | rs7766973 |
| MSV3d | rs7766973 |
| GWAS Ctlg | rs7766973 |
| GMAF | 0.4582 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs7766973 is a SNP in the jumonji, AT rich interactive domain 2 JARID2 gene.
Significantly (p = 2 x 10e-7) but weakly associated with autism based on a GWAS study of 1,000+ affected families. However, upon attempted replication, rs7766973 did not meet genome-wide significance.[PMID 19812673
]
Nonetheless, a French company (Integragen) announced in 2011 ([1] that is was licensing the use of this SNP for identifying children at increased risk for autism, perhaps by combining rs7766973 with other autism-related SNPs.
