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rs199473635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473635(C;T)
Make rs199473635(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550896
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473635
ebirs199473635
HLIrs199473635
Exacrs199473635
Varsomers199473635
Maprs199473635
PheGenIrs199473635
hapmaprs199473635
1000 genomesrs199473635
hgdprs199473635
ensemblrs199473635
gopubmedrs199473635
geneviewrs199473635
scholarrs199473635
googlers199473635
pharmgkbrs199473635
gwascentralrs199473635
openSNPrs199473635
23andMers199473635
23andMe allrs199473635
SNP Nexus

SNPshotrs199473635
SNPdbers199473635
MSV3drs199473635
GWAS Ctlgrs199473635
Max Magnitude0
ClinVar
Risk rs199473635(T;T)
Alt rs199473635(T;T)
Reference rs199473635(C;C)
Significance Probable-Pathogenic
Disease Atrial fibrillation not provided
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation not provided
Reversed 1
HGVS NC_000003.11:g.38592387G>A
CLNSRC ClinVar
CLNACC RCV000058785.2, RCV000183122.1,