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rs199473627

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473627(C;C)
Make rs199473627(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551258
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473627
ebirs199473627
HLIrs199473627
Exacrs199473627
Varsomers199473627
Maprs199473627
PheGenIrs199473627
hapmaprs199473627
1000 genomesrs199473627
hgdprs199473627
ensemblrs199473627
gopubmedrs199473627
geneviewrs199473627
scholarrs199473627
googlers199473627
pharmgkbrs199473627
gwascentralrs199473627
openSNPrs199473627
23andMers199473627
23andMe allrs199473627
SNP Nexus

SNPshotrs199473627
SNPdbers199473627
MSV3drs199473627
GWAS Ctlgrs199473627
Max Magnitude0
ClinVar
Risk rs199473627(C;C)
Alt rs199473627(C;C)
Reference rs199473627(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.38592749A>G
CLNSRC ClinVar
CLNACC RCV000058739.2,