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rs199473297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473297(C;T)
Make rs199473297(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551246
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473297
ebirs199473297
HLIrs199473297
Exacrs199473297
Varsomers199473297
Maprs199473297
PheGenIrs199473297
hapmaprs199473297
1000 genomesrs199473297
hgdprs199473297
ensemblrs199473297
gopubmedrs199473297
geneviewrs199473297
scholarrs199473297
googlers199473297
pharmgkbrs199473297
gwascentralrs199473297
openSNPrs199473297
23andMers199473297
23andMe allrs199473297
SNP Nexus

SNPshotrs199473297
SNPdbers199473297
MSV3drs199473297
GWAS Ctlgrs199473297
Max Magnitude0
ClinVar
Risk rs199473297(G,T;G,T)
Alt rs199473297(G,T;G,T)
Reference rs199473297(C;C)
Significance Pathogenic
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38592737G>A; NC_000003.11:g.38592737G>C
CLNSRC ClinVar
CLNACC RCV000058742.2, RCV000183101.2, RCV000058741.2,