rs931949929
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs931949929(A;A) |
| Make rs931949929(A;T) |
| Make rs931949929(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 35033607 |
| Gene | SCN1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs931949929 |
| dbSNP (classic) | rs931949929 |
| ClinGen | rs931949929 |
| ebi | rs931949929 |
| HLI | rs931949929 |
| Exac | rs931949929 |
| Gnomad | rs931949929 |
| Varsome | rs931949929 |
| LitVar | rs931949929 |
| Map | rs931949929 |
| PheGenI | rs931949929 |
| Biobank | rs931949929 |
| 1000 genomes | rs931949929 |
| hgdp | rs931949929 |
| ensembl | rs931949929 |
| geneview | rs931949929 |
| scholar | rs931949929 |
| rs931949929 | |
| pharmgkb | rs931949929 |
| gwascentral | rs931949929 |
| openSNP | rs931949929 |
| 23andMe | rs931949929 |
| SNPshot | rs931949929 |
| SNPdbe | rs931949929 |
| MSV3d | rs931949929 |
| GWAS Ctlg | rs931949929 |
| Max Magnitude | 0 |
aka NM_001037.4(SCN1B):c.316A>T or (p.Ile106Phe)
OMIM pathogenic variant
