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