rs774452124
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
Make rs774452124(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 63941958 |
Gene | SCN4A |
is a | snp |
is | mentioned by |
dbSNP | rs774452124 |
dbSNP (classic) | rs774452124 |
ClinGen | rs774452124 |
ebi | rs774452124 |
HLI | rs774452124 |
Exac | rs774452124 |
Gnomad | rs774452124 |
Varsome | rs774452124 |
LitVar | rs774452124 |
Map | rs774452124 |
PheGenI | rs774452124 |
Biobank | rs774452124 |
1000 genomes | rs774452124 |
hgdp | rs774452124 |
ensembl | rs774452124 |
geneview | rs774452124 |
scholar | rs774452124 |
rs774452124 | |
pharmgkb | rs774452124 |
gwascentral | rs774452124 |
openSNP | rs774452124 |
23andMe | rs774452124 |
SNPshot | rs774452124 |
SNPdbe | rs774452124 |
MSV3d | rs774452124 |
GWAS Ctlg | rs774452124 |
Max Magnitude | 0 |
aka c.4324G>A (p.Val1442Met)
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