rs1896731
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1896731(C;C) |
| Make rs1896731(C;T) |
| Make rs1896731(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 25898911 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1896731 |
| dbSNP (classic) | rs1896731 |
| ClinGen | rs1896731 |
| ebi | rs1896731 |
| HLI | rs1896731 |
| Exac | rs1896731 |
| Gnomad | rs1896731 |
| Varsome | rs1896731 |
| LitVar | rs1896731 |
| Map | rs1896731 |
| PheGenI | rs1896731 |
| Biobank | rs1896731 |
| 1000 genomes | rs1896731 |
| hgdp | rs1896731 |
| ensembl | rs1896731 |
| geneview | rs1896731 |
| scholar | rs1896731 |
| rs1896731 | |
| pharmgkb | rs1896731 |
| gwascentral | rs1896731 |
| openSNP | rs1896731 |
| 23andMe | rs1896731 |
| SNPshot | rs1896731 |
| SNPdbe | rs1896731 |
| MSV3d | rs1896731 |
| GWAS Ctlg | rs1896731 |
| GMAF | 0.4449 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19456320
] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
