rs751368967
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 2.9 | SIDS predisposition?? |
| (G;G) | 0 | common/normal |
| Make rs751368967(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 63957493 |
| Gene | LOC105371858, SCN4A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs751368967 |
| dbSNP (classic) | rs751368967 |
| ClinGen | rs751368967 |
| ebi | rs751368967 |
| HLI | rs751368967 |
| Exac | rs751368967 |
| Gnomad | rs751368967 |
| Varsome | rs751368967 |
| LitVar | rs751368967 |
| Map | rs751368967 |
| PheGenI | rs751368967 |
| Biobank | rs751368967 |
| 1000 genomes | rs751368967 |
| hgdp | rs751368967 |
| ensembl | rs751368967 |
| geneview | rs751368967 |
| scholar | rs751368967 |
| rs751368967 | |
| pharmgkb | rs751368967 |
| gwascentral | rs751368967 |
| openSNP | rs751368967 |
| 23andMe | rs751368967 |
| SNPshot | rs751368967 |
| SNPdbe | rs751368967 |
| MSV3d | rs751368967 |
| GWAS Ctlg | rs751368967 |
| Max Magnitude | 2.9 |
aka c.2045C>G (p.Ser682Trp)
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
