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rs199473564

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473564(C;C)
Make rs199473564(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38608205
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473564
ebirs199473564
HLIrs199473564
Exacrs199473564
Varsomers199473564
Maprs199473564
PheGenIrs199473564
hapmaprs199473564
1000 genomesrs199473564
hgdprs199473564
ensemblrs199473564
gopubmedrs199473564
geneviewrs199473564
scholarrs199473564
googlers199473564
pharmgkbrs199473564
gwascentralrs199473564
openSNPrs199473564
23andMers199473564
23andMe allrs199473564
SNP Nexus

SNPshotrs199473564
SNPdbers199473564
MSV3drs199473564
GWAS Ctlgrs199473564
Max Magnitude0
ClinVar
Risk rs199473564(C;C)
Alt rs199473564(C;C)
Reference rs199473564(T;T)
Significance Other
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38649696A>G
CLNSRC ClinVar
CLNACC RCV000058862.3, RCV000182953.1,