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rs199473252

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473252(A;A)
Make rs199473252(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38556526
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473252
ebirs199473252
HLIrs199473252
Exacrs199473252
Varsomers199473252
Maprs199473252
PheGenIrs199473252
hapmaprs199473252
1000 genomesrs199473252
hgdprs199473252
ensemblrs199473252
gopubmedrs199473252
geneviewrs199473252
scholarrs199473252
googlers199473252
pharmgkbrs199473252
gwascentralrs199473252
openSNPrs199473252
23andMers199473252
23andMe allrs199473252
SNP Nexus

SNPshotrs199473252
SNPdbers199473252
MSV3drs199473252
GWAS Ctlgrs199473252
Max Magnitude0
ClinVar
Risk rs199473252(A;A)
Alt rs199473252(A;A)
Reference rs199473252(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38598017A>T
CLNSRC ClinVar
CLNACC RCV000058665.2,