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rs199473324

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473324(C;C)
Make rs199473324(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550748
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473324
ebirs199473324
HLIrs199473324
Exacrs199473324
Varsomers199473324
Maprs199473324
PheGenIrs199473324
hapmaprs199473324
1000 genomesrs199473324
hgdprs199473324
ensemblrs199473324
gopubmedrs199473324
geneviewrs199473324
scholarrs199473324
googlers199473324
pharmgkbrs199473324
gwascentralrs199473324
openSNPrs199473324
23andMers199473324
23andMe allrs199473324
SNP Nexus

SNPshotrs199473324
SNPdbers199473324
MSV3drs199473324
GWAS Ctlgrs199473324
Max Magnitude0
ClinVar
Risk rs199473324(A,C;A,C)
Alt rs199473324(A,C;A,C)
Reference rs199473324(T;T)
Significance Pathogenic
Disease Atrial fibrillation not provided
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation not provided
Reversed 1
HGVS NC_000003.11:g.38592239A>G
CLNSRC ClinVar
CLNACC RCV000058796.2, RCV000183128.2,