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rs774453167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 2.9 SIDS predisposition??
Make rs774453167(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome17
Position63941895
GeneSCN4A
is asnp
is mentioned by
dbSNPrs774453167
dbSNP (classic)rs774453167
ClinGenrs774453167
ebirs774453167
HLIrs774453167
Exacrs774453167
Gnomadrs774453167
Varsomers774453167
LitVarrs774453167
Maprs774453167
PheGenIrs774453167
Biobankrs774453167
1000 genomesrs774453167
hgdprs774453167
ensemblrs774453167
geneviewrs774453167
scholarrs774453167
googlers774453167
pharmgkbrs774453167
gwascentralrs774453167
openSNPrs774453167
23andMers774453167
SNPshotrs774453167
SNPdbers774453167
MSV3drs774453167
GWAS Ctlgrs774453167
Max Magnitude2.9

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