rs758906955
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs758906955(C;C) |
| Make rs758906955(C;T) |
| Make rs758906955(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 165097377 |
| Gene | SCN3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs758906955 |
| dbSNP (classic) | rs758906955 |
| ClinGen | rs758906955 |
| ebi | rs758906955 |
| HLI | rs758906955 |
| Exac | rs758906955 |
| Gnomad | rs758906955 |
| Varsome | rs758906955 |
| LitVar | rs758906955 |
| Map | rs758906955 |
| PheGenI | rs758906955 |
| Biobank | rs758906955 |
| 1000 genomes | rs758906955 |
| hgdp | rs758906955 |
| ensembl | rs758906955 |
| geneview | rs758906955 |
| scholar | rs758906955 |
| rs758906955 | |
| pharmgkb | rs758906955 |
| gwascentral | rs758906955 |
| openSNP | rs758906955 |
| 23andMe | rs758906955 |
| SNPshot | rs758906955 |
| SNPdbe | rs758906955 |
| MSV3d | rs758906955 |
| GWAS Ctlg | rs758906955 |
| Max Magnitude | 0 |
aka NM_006922.3(SCN3A):c.4114A>G or (p.Met1372Val)
OMIM pathogenic variant
