rs774195502
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs774195502(C;C) |
| Make rs774195502(C;T) |
| Make rs774195502(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 165155865 |
| Gene | SCN3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774195502 |
| dbSNP (classic) | rs774195502 |
| ClinGen | rs774195502 |
| ebi | rs774195502 |
| HLI | rs774195502 |
| Exac | rs774195502 |
| Gnomad | rs774195502 |
| Varsome | rs774195502 |
| LitVar | rs774195502 |
| Map | rs774195502 |
| PheGenI | rs774195502 |
| Biobank | rs774195502 |
| 1000 genomes | rs774195502 |
| hgdp | rs774195502 |
| ensembl | rs774195502 |
| geneview | rs774195502 |
| scholar | rs774195502 |
| rs774195502 | |
| pharmgkb | rs774195502 |
| gwascentral | rs774195502 |
| openSNP | rs774195502 |
| 23andMe | rs774195502 |
| SNPshot | rs774195502 |
| SNPdbe | rs774195502 |
| MSV3d | rs774195502 |
| GWAS Ctlg | rs774195502 |
| Max Magnitude | 0 |
aka NM_006922.3(SCN3A):c.1070G>A or (p.Arg357Gln)
OMIM pathogenic variant
