rs1859767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs1859767(A;T) |
| Make rs1859767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 108447879 |
| Gene | NRCAM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1859767 |
| dbSNP (classic) | rs1859767 |
| ClinGen | rs1859767 |
| ebi | rs1859767 |
| HLI | rs1859767 |
| Exac | rs1859767 |
| Gnomad | rs1859767 |
| Varsome | rs1859767 |
| LitVar | rs1859767 |
| Map | rs1859767 |
| PheGenI | rs1859767 |
| Biobank | rs1859767 |
| 1000 genomes | rs1859767 |
| hgdp | rs1859767 |
| ensembl | rs1859767 |
| geneview | rs1859767 |
| scholar | rs1859767 |
| rs1859767 | |
| pharmgkb | rs1859767 |
| gwascentral | rs1859767 |
| openSNP | rs1859767 |
| 23andMe | rs1859767 |
| SNPshot | rs1859767 |
| SNPdbe | rs1859767 |
| MSV3d | rs1859767 |
| GWAS Ctlg | rs1859767 |
| GMAF | 0.3673 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18664314] Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism
