rs781379291
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs781379291(A;A) |
| Make rs781379291(A;G) |
| Make rs781379291(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 35292512 |
| Gene | SLC1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs781379291 |
| dbSNP (classic) | rs781379291 |
| ClinGen | rs781379291 |
| ebi | rs781379291 |
| HLI | rs781379291 |
| Exac | rs781379291 |
| Gnomad | rs781379291 |
| Varsome | rs781379291 |
| LitVar | rs781379291 |
| Map | rs781379291 |
| PheGenI | rs781379291 |
| Biobank | rs781379291 |
| 1000 genomes | rs781379291 |
| hgdp | rs781379291 |
| ensembl | rs781379291 |
| geneview | rs781379291 |
| scholar | rs781379291 |
| rs781379291 | |
| pharmgkb | rs781379291 |
| gwascentral | rs781379291 |
| openSNP | rs781379291 |
| 23andMe | rs781379291 |
| SNPshot | rs781379291 |
| SNPdbe | rs781379291 |
| MSV3d | rs781379291 |
| GWAS Ctlg | rs781379291 |
| Max Magnitude | 0 |
aka NM_004171.3(SLC1A2):c.866C>G or (p.Pro289Arg)
OMIM pathogenic variant
