rs2229864
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2229864(C;C) |
| Make rs2229864(C;T) |
| Make rs2229864(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103515258 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2229864 |
| dbSNP (classic) | rs2229864 |
| ClinGen | rs2229864 |
| ebi | rs2229864 |
| HLI | rs2229864 |
| Exac | rs2229864 |
| Gnomad | rs2229864 |
| Varsome | rs2229864 |
| LitVar | rs2229864 |
| Map | rs2229864 |
| PheGenI | rs2229864 |
| Biobank | rs2229864 |
| 1000 genomes | rs2229864 |
| hgdp | rs2229864 |
| ensembl | rs2229864 |
| geneview | rs2229864 |
| scholar | rs2229864 |
| rs2229864 | |
| pharmgkb | rs2229864 |
| gwascentral | rs2229864 |
| openSNP | rs2229864 |
| 23andMe | rs2229864 |
| SNPshot | rs2229864 |
| SNPdbe | rs2229864 |
| MSV3d | rs2229864 |
| GWAS Ctlg | rs2229864 |
| GMAF | 0.4256 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20554015] No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population
| ClinVar | |
|---|---|
| Risk | rs2229864(C;C) |
| Alt | rs2229864(C;C) |
| Reference | rs2229864(T;T) |
| Significance | Other |
| Disease | not specified Lissencephaly |
| Variation | info |
| Gene | RELN |
| CLNDBN | not specified Lissencephaly, Recessive |
| Reversed | 1 |
| HGVS | NC_000007.13:g.103155705A>G |
| CLNSRC | ClinVar Emory University University of Chicago |
| CLNACC | RCV000081242.8, RCV000404542.1, |
[PMID 29753726] Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.
