rs774453167
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common/normal |
| (G;T) | 2.9 | SIDS predisposition?? |
| Make rs774453167(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 63941895 |
| Gene | SCN4A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774453167 |
| dbSNP (classic) | rs774453167 |
| ClinGen | rs774453167 |
| ebi | rs774453167 |
| HLI | rs774453167 |
| Exac | rs774453167 |
| Gnomad | rs774453167 |
| Varsome | rs774453167 |
| LitVar | rs774453167 |
| Map | rs774453167 |
| PheGenI | rs774453167 |
| Biobank | rs774453167 |
| 1000 genomes | rs774453167 |
| hgdp | rs774453167 |
| ensembl | rs774453167 |
| geneview | rs774453167 |
| scholar | rs774453167 |
| rs774453167 | |
| pharmgkb | rs774453167 |
| gwascentral | rs774453167 |
| openSNP | rs774453167 |
| 23andMe | rs774453167 |
| SNPshot | rs774453167 |
| SNPdbe | rs774453167 |
| MSV3d | rs774453167 |
| GWAS Ctlg | rs774453167 |
| Max Magnitude | 2.9 |
aka c.4387C>A (p.Arg1463Ser)
10.1016/S0140-6736(18)30021-7 Possible association of minor allele of this SCN4A gene variant with predisposition to Sudden Infant Death Syndrome, based on exome analysis
