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rs199473632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473632(A;G)
Make rs199473632(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551072
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473632
ebirs199473632
HLIrs199473632
Exacrs199473632
Varsomers199473632
Maprs199473632
PheGenIrs199473632
hapmaprs199473632
1000 genomesrs199473632
hgdprs199473632
ensemblrs199473632
gopubmedrs199473632
geneviewrs199473632
scholarrs199473632
googlers199473632
pharmgkbrs199473632
gwascentralrs199473632
openSNPrs199473632
23andMers199473632
23andMe allrs199473632
SNP Nexus

SNPshotrs199473632
SNPdbers199473632
MSV3drs199473632
GWAS Ctlgrs199473632
Max Magnitude0
ClinVar
Risk rs199473632(G;G)
Alt rs199473632(G;G)
Reference rs199473632(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.38592563T>C
CLNSRC ClinVar
CLNACC RCV000058765.2,