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rs199473052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473052(C;C)
Make rs199473052(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38630425
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473052
ebirs199473052
HLIrs199473052
Exacrs199473052
Varsomers199473052
Maprs199473052
PheGenIrs199473052
hapmaprs199473052
1000 genomesrs199473052
hgdprs199473052
ensemblrs199473052
gopubmedrs199473052
geneviewrs199473052
scholarrs199473052
googlers199473052
pharmgkbrs199473052
gwascentralrs199473052
openSNPrs199473052
23andMers199473052
23andMe allrs199473052
SNP Nexus

SNPshotrs199473052
SNPdbers199473052
MSV3drs199473052
GWAS Ctlgrs199473052
Max Magnitude0
ClinVar
Risk rs199473052(C;C)
Alt rs199473052(C;C)
Reference rs199473052(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38671916A>G
CLNSRC ClinVar
CLNACC RCV000058528.2,