Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473335(A;A)
Make rs199473335(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position38550411
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473335
ebirs199473335
HLIrs199473335
Exacrs199473335
Varsomers199473335
Maprs199473335
PheGenIrs199473335
hapmaprs199473335
1000 genomesrs199473335
hgdprs199473335
ensemblrs199473335
gopubmedrs199473335
geneviewrs199473335
scholarrs199473335
googlers199473335
pharmgkbrs199473335
gwascentralrs199473335
openSNPrs199473335
23andMers199473335
23andMe allrs199473335
SNP Nexus

SNPshotrs199473335
SNPdbers199473335
MSV3drs199473335
GWAS Ctlgrs199473335
Max Magnitude0
ClinVar
Risk rs199473335(A;A)
Alt rs199473335(A;A)
Reference rs199473335(C;C)
Significance Pathogenic
Disease Atrial fibrillation Atrial fibrillation not specified
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation, familial, 10 Atrial fibrillation not specified
Reversed 1
HGVS NC_000003.11:g.38591902G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022947.2, RCV000058818.2, RCV000148858.1, RCV000154830.1,