rs755440336
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs755440336(C;C) |
| Make rs755440336(C;T) |
| Make rs755440336(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 165131366 |
| Gene | SCN3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs755440336 |
| dbSNP (classic) | rs755440336 |
| ClinGen | rs755440336 |
| ebi | rs755440336 |
| HLI | rs755440336 |
| Exac | rs755440336 |
| Gnomad | rs755440336 |
| Varsome | rs755440336 |
| LitVar | rs755440336 |
| Map | rs755440336 |
| PheGenI | rs755440336 |
| Biobank | rs755440336 |
| 1000 genomes | rs755440336 |
| hgdp | rs755440336 |
| ensembl | rs755440336 |
| geneview | rs755440336 |
| scholar | rs755440336 |
| rs755440336 | |
| pharmgkb | rs755440336 |
| gwascentral | rs755440336 |
| openSNP | rs755440336 |
| 23andMe | rs755440336 |
| SNPshot | rs755440336 |
| SNPdbe | rs755440336 |
| MSV3d | rs755440336 |
| GWAS Ctlg | rs755440336 |
| Max Magnitude | 0 |
aka NM_006922.3(SCN3A):c.2443G>A or (p.Asp815Asn)
OMIM pathogenic variant
