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rs199473551

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473551(A;G)
Make rs199473551(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38633219
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473551
ebirs199473551
HLIrs199473551
Exacrs199473551
Varsomers199473551
Maprs199473551
PheGenIrs199473551
hapmaprs199473551
1000 genomesrs199473551
hgdprs199473551
ensemblrs199473551
gopubmedrs199473551
geneviewrs199473551
scholarrs199473551
googlers199473551
pharmgkbrs199473551
gwascentralrs199473551
openSNPrs199473551
23andMers199473551
23andMe allrs199473551
SNP Nexus

SNPshotrs199473551
SNPdbers199473551
MSV3drs199473551
GWAS Ctlgrs199473551
Max Magnitude0
ClinVar
Risk rs199473551(G;G)
Alt rs199473551(G;G)
Reference rs199473551(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38674710T>C
CLNSRC ClinVar
CLNACC RCV000058861.2,