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rs140348243

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140348243(A;A)
Make rs140348243(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position118137097
GeneSCN4B
is asnp
is mentioned by
dbSNPrs140348243
ebirs140348243
HLIrs140348243
Exacrs140348243
Varsomers140348243
Maprs140348243
PheGenIrs140348243
hapmaprs140348243
1000 genomesrs140348243
hgdprs140348243
ensemblrs140348243
gopubmedrs140348243
geneviewrs140348243
scholarrs140348243
googlers140348243
pharmgkbrs140348243
gwascentralrs140348243
openSNPrs140348243
23andMers140348243
23andMe allrs140348243
SNP Nexus

SNPshotrs140348243
SNPdbers140348243
MSV3drs140348243
GWAS Ctlgrs140348243
Max Magnitude0
ClinVar
Risk rs140348243(A;A)
Alt rs140348243(A;A)
Reference rs140348243(G;G)
Significance Probable-Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME Long QT syndrome 10
Variation info
Gene SCN4B
CLNDBN SUDDEN INFANT DEATH SYNDROME Long QT syndrome 10
Reversed 0
HGVS NC_000011.9:g.118007812G>A
CLNSRC
CLNACC RCV000171568.1, RCV000234662.1,