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rs199473166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473166(A;T)
Make rs199473166(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585936
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473166
ebirs199473166
HLIrs199473166
Exacrs199473166
Varsomers199473166
Maprs199473166
PheGenIrs199473166
hapmaprs199473166
1000 genomesrs199473166
hgdprs199473166
ensemblrs199473166
gopubmedrs199473166
geneviewrs199473166
scholarrs199473166
googlers199473166
pharmgkbrs199473166
gwascentralrs199473166
openSNPrs199473166
23andMers199473166
23andMe allrs199473166
SNP Nexus

SNPshotrs199473166
SNPdbers199473166
MSV3drs199473166
GWAS Ctlgrs199473166
Max Magnitude0
ClinVar
Risk rs199473166(T;T)
Alt rs199473166(T;T)
Reference rs199473166(A;A)
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.38627427T>A
CLNSRC ClinVar
CLNACC RCV000058509.2, RCV000183004.3,