rs736707
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs736707(C;C) |
| Make rs736707(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103489956 |
| Gene | LOC101927870, RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs736707 |
| dbSNP (classic) | rs736707 |
| ClinGen | rs736707 |
| ebi | rs736707 |
| HLI | rs736707 |
| Exac | rs736707 |
| Gnomad | rs736707 |
| Varsome | rs736707 |
| LitVar | rs736707 |
| Map | rs736707 |
| PheGenI | rs736707 |
| Biobank | rs736707 |
| 1000 genomes | rs736707 |
| hgdp | rs736707 |
| ensembl | rs736707 |
| geneview | rs736707 |
| scholar | rs736707 |
| rs736707 | |
| pharmgkb | rs736707 |
| gwascentral | rs736707 |
| openSNP | rs736707 |
| 23andMe | rs736707 |
| SNPshot | rs736707 |
| SNPdbe | rs736707 |
| MSV3d | rs736707 |
| GWAS Ctlg | rs736707 |
| GMAF | 0.3407 |
| 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
[PMID 18597938] Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
[PMID 23216241
] Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
[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.
