Have questions? Visit https://www.reddit.com/r/SNPedia

rs774452124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
Make rs774452124(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome17
Position63941958
GeneSCN4A
is asnp
is mentioned by
dbSNPrs774452124
dbSNP (classic)rs774452124
ClinGenrs774452124
ebirs774452124
HLIrs774452124
Exacrs774452124
Gnomadrs774452124
Varsomers774452124
LitVarrs774452124
Maprs774452124
PheGenIrs774452124
Biobankrs774452124
1000 genomesrs774452124
hgdprs774452124
ensemblrs774452124
geneviewrs774452124
scholarrs774452124
googlers774452124
pharmgkbrs774452124
gwascentralrs774452124
openSNPrs774452124
23andMers774452124
23andMe allrs774452124
SNPshotrs774452124
SNPdbers774452124
MSV3drs774452124
GWAS Ctlgrs774452124
Max Magnitude0

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