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rs199473286

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473286(A;A)
Make rs199473286(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551477
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473286
ebirs199473286
HLIrs199473286
Exacrs199473286
Varsomers199473286
Maprs199473286
PheGenIrs199473286
hapmaprs199473286
1000 genomesrs199473286
hgdprs199473286
ensemblrs199473286
gopubmedrs199473286
geneviewrs199473286
scholarrs199473286
googlers199473286
pharmgkbrs199473286
gwascentralrs199473286
openSNPrs199473286
23andMers199473286
23andMe allrs199473286
SNP Nexus

SNPshotrs199473286
SNPdbers199473286
MSV3drs199473286
GWAS Ctlgrs199473286
Max Magnitude0
ClinVar
Risk rs199473286(A;A)
Alt rs199473286(A;A)
Reference rs199473286(G;G)
Significance Pathogenic
Disease Cardiac conduction defect
Variation info
Gene SCN5A
CLNDBN Cardiac conduction defect, nonspecific
Reversed 1
HGVS NC_000003.11:g.38592968C>T
CLNSRC ClinVar
CLNACC RCV000058723.2,