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rs199473630

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473630(A;A)
Make rs199473630(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551133
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473630
ebirs199473630
HLIrs199473630
Exacrs199473630
Varsomers199473630
Maprs199473630
PheGenIrs199473630
hapmaprs199473630
1000 genomesrs199473630
hgdprs199473630
ensemblrs199473630
gopubmedrs199473630
geneviewrs199473630
scholarrs199473630
googlers199473630
pharmgkbrs199473630
gwascentralrs199473630
openSNPrs199473630
23andMers199473630
23andMe allrs199473630
SNP Nexus

SNPshotrs199473630
SNPdbers199473630
MSV3drs199473630
GWAS Ctlgrs199473630
Max Magnitude0
ClinVar
Risk rs199473630(A;A)
Alt rs199473630(A;A)
Reference rs199473630(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not specified
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38592624C>T
CLNSRC ClinVar
CLNACC RCV000058756.2, RCV000183111.2,