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rs199473162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473162(A;A)
Make rs199473162(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38586031
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473162
ebirs199473162
HLIrs199473162
Exacrs199473162
Varsomers199473162
Maprs199473162
PheGenIrs199473162
hapmaprs199473162
1000 genomesrs199473162
hgdprs199473162
ensemblrs199473162
gopubmedrs199473162
geneviewrs199473162
scholarrs199473162
googlers199473162
pharmgkbrs199473162
gwascentralrs199473162
openSNPrs199473162
23andMers199473162
23andMe allrs199473162
SNP Nexus

SNPshotrs199473162
SNPdbers199473162
MSV3drs199473162
GWAS Ctlgrs199473162
Max Magnitude0
ClinVar
Risk rs199473162(A;A)
Alt rs199473162(A;A)
Reference rs199473162(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38627522A>T
CLNSRC ClinVar
CLNACC RCV000058502.2,