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rs199473142

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473142(A;A)
Make rs199473142(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38597952
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473142
ebirs199473142
HLIrs199473142
Exacrs199473142
Varsomers199473142
Maprs199473142
PheGenIrs199473142
hapmaprs199473142
1000 genomesrs199473142
hgdprs199473142
ensemblrs199473142
gopubmedrs199473142
geneviewrs199473142
scholarrs199473142
googlers199473142
pharmgkbrs199473142
gwascentralrs199473142
openSNPrs199473142
23andMers199473142
23andMe allrs199473142
SNP Nexus

SNPshotrs199473142
SNPdbers199473142
MSV3drs199473142
GWAS Ctlgrs199473142
Max Magnitude0
ClinVar
Risk rs199473142(A;A)
Alt rs199473142(A;A)
Reference rs199473142(G;G)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME not specified
Variation info
Gene SCN5A
CLNDBN SUDDEN INFANT DEATH SYNDROME not specified
Reversed 1
HGVS NC_000003.11:g.38639443C>T
CLNSRC ClinVar
CLNACC RCV000058473.2, RCV000156507.1,