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rs199473306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473306(A;A)
Make rs199473306(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551136
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473306
ebirs199473306
HLIrs199473306
Exacrs199473306
Varsomers199473306
Maprs199473306
PheGenIrs199473306
hapmaprs199473306
1000 genomesrs199473306
hgdprs199473306
ensemblrs199473306
gopubmedrs199473306
geneviewrs199473306
scholarrs199473306
googlers199473306
pharmgkbrs199473306
gwascentralrs199473306
openSNPrs199473306
23andMers199473306
23andMe allrs199473306
SNP Nexus

SNPshotrs199473306
SNPdbers199473306
MSV3drs199473306
GWAS Ctlgrs199473306
Max Magnitude0
ClinVar
Risk rs199473306(A;A)
Alt rs199473306(A;A)
Reference rs199473306(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38592627C>T
CLNSRC ClinVar
CLNACC RCV000058755.2,