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rs199473300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473300(A;A)
Make rs199473300(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551204
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473300
ebirs199473300
HLIrs199473300
Exacrs199473300
Varsomers199473300
Maprs199473300
PheGenIrs199473300
hapmaprs199473300
1000 genomesrs199473300
hgdprs199473300
ensemblrs199473300
gopubmedrs199473300
geneviewrs199473300
scholarrs199473300
googlers199473300
pharmgkbrs199473300
gwascentralrs199473300
openSNPrs199473300
23andMers199473300
23andMe allrs199473300
SNP Nexus

SNPshotrs199473300
SNPdbers199473300
MSV3drs199473300
GWAS Ctlgrs199473300
Max Magnitude0
ClinVar
Risk rs199473300(A;A)
Alt rs199473300(A;A)
Reference rs199473300(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38592695G>T
CLNSRC ClinVar
CLNACC RCV000058747.2, RCV000183106.1,