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rs199473555

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473555(A;A)
Make rs199473555(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38630366
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473555
ebirs199473555
HLIrs199473555
Exacrs199473555
Varsomers199473555
Maprs199473555
PheGenIrs199473555
hapmaprs199473555
1000 genomesrs199473555
hgdprs199473555
ensemblrs199473555
gopubmedrs199473555
geneviewrs199473555
scholarrs199473555
googlers199473555
pharmgkbrs199473555
gwascentralrs199473555
openSNPrs199473555
23andMers199473555
23andMe allrs199473555
SNP Nexus

SNPshotrs199473555
SNPdbers199473555
MSV3drs199473555
GWAS Ctlgrs199473555
Max Magnitude0
ClinVar
Risk rs199473555(A;A)
Alt rs199473555(A;A)
Reference rs199473555(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.38671857C>T
CLNSRC ClinVar
CLNACC RCV000058568.2,