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rs199473069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473069(A;A)
Make rs199473069(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620885
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473069
ebirs199473069
HLIrs199473069
Exacrs199473069
Varsomers199473069
Maprs199473069
PheGenIrs199473069
hapmaprs199473069
1000 genomesrs199473069
hgdprs199473069
ensemblrs199473069
gopubmedrs199473069
geneviewrs199473069
scholarrs199473069
googlers199473069
pharmgkbrs199473069
gwascentralrs199473069
openSNPrs199473069
23andMers199473069
23andMe allrs199473069
SNP Nexus

SNPshotrs199473069
SNPdbers199473069
MSV3drs199473069
GWAS Ctlgrs199473069
Max Magnitude0
ClinVar
Risk rs199473069(A,T;A,T)
Alt rs199473069(A,T;A,T)
Reference rs199473069(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.38662376C>T
CLNSRC ClinVar
CLNACC RCV000058799.2, RCV000182933.2,