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rs199473311

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473311(A;G)
Make rs199473311(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551070
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473311
ebirs199473311
HLIrs199473311
Exacrs199473311
Varsomers199473311
Maprs199473311
PheGenIrs199473311
hapmaprs199473311
1000 genomesrs199473311
hgdprs199473311
ensemblrs199473311
gopubmedrs199473311
geneviewrs199473311
scholarrs199473311
googlers199473311
pharmgkbrs199473311
gwascentralrs199473311
openSNPrs199473311
23andMers199473311
23andMe allrs199473311
SNP Nexus

SNPshotrs199473311
SNPdbers199473311
MSV3drs199473311
GWAS Ctlgrs199473311
Max Magnitude0
ClinVar
Risk rs199473311(G;G)
Alt rs199473311(G;G)
Reference rs199473311(A;A)
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.38592561T>C
CLNSRC ClinVar
CLNACC RCV000058766.2, RCV000183198.2,