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rs199473615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473615(C;C)
Make rs199473615(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555742
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473615
ebirs199473615
HLIrs199473615
Exacrs199473615
Varsomers199473615
Maprs199473615
PheGenIrs199473615
hapmaprs199473615
1000 genomesrs199473615
hgdprs199473615
ensemblrs199473615
gopubmedrs199473615
geneviewrs199473615
scholarrs199473615
googlers199473615
pharmgkbrs199473615
gwascentralrs199473615
openSNPrs199473615
23andMers199473615
23andMe allrs199473615
SNP Nexus

SNPshotrs199473615
SNPdbers199473615
MSV3drs199473615
GWAS Ctlgrs199473615
Max Magnitude0
ClinVar
Risk rs199473615(C;C)
Alt rs199473615(C;C)
Reference rs199473615(T;T)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene SCN5A
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000003.11:g.38597233A>G
CLNSRC ClinVar
CLNACC RCV000058674.2,