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rs199473239

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473239(C;C)
Make rs199473239(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560179
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473239
ebirs199473239
HLIrs199473239
Exacrs199473239
Varsomers199473239
Maprs199473239
PheGenIrs199473239
hapmaprs199473239
1000 genomesrs199473239
hgdprs199473239
ensemblrs199473239
gopubmedrs199473239
geneviewrs199473239
scholarrs199473239
googlers199473239
pharmgkbrs199473239
gwascentralrs199473239
openSNPrs199473239
23andMers199473239
23andMe allrs199473239
SNP Nexus

SNPshotrs199473239
SNPdbers199473239
MSV3drs199473239
GWAS Ctlgrs199473239
Max Magnitude0
ClinVar
Risk rs199473239(A,C;A,C)
Alt rs199473239(A,C;A,C)
Reference rs199473239(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38601670C>G; NC_000003.11:g.38601670C>T
CLNSRC ClinVar
CLNACC RCV000058646.2, RCV000058645.2,