rs1234747
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1234747(A;A) |
| Make rs1234747(A;G) |
| Make rs1234747(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 147795900 |
| Gene | SAMD5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1234747 |
| dbSNP (classic) | rs1234747 |
| ClinGen | rs1234747 |
| ebi | rs1234747 |
| HLI | rs1234747 |
| Exac | rs1234747 |
| Gnomad | rs1234747 |
| Varsome | rs1234747 |
| LitVar | rs1234747 |
| Map | rs1234747 |
| PheGenI | rs1234747 |
| Biobank | rs1234747 |
| 1000 genomes | rs1234747 |
| hgdp | rs1234747 |
| ensembl | rs1234747 |
| geneview | rs1234747 |
| scholar | rs1234747 |
| rs1234747 | |
| pharmgkb | rs1234747 |
| gwascentral | rs1234747 |
| openSNP | rs1234747 |
| 23andMe | rs1234747 |
| SNPshot | rs1234747 |
| SNPdbe | rs1234747 |
| MSV3d | rs1234747 |
| GWAS Ctlg | rs1234747 |
| Max Magnitude | 0 |
nature The inheritance of the AC haplotype of rs1861972 – rs1861973, the C allele of rs1811399, and the C allele of rs1234747 may contribute to autism by affecting microRNA
