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rs199473199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473199(C;C)
Make rs199473199(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38576753
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473199
ebirs199473199
HLIrs199473199
Exacrs199473199
Varsomers199473199
Maprs199473199
PheGenIrs199473199
hapmaprs199473199
1000 genomesrs199473199
hgdprs199473199
ensemblrs199473199
gopubmedrs199473199
geneviewrs199473199
scholarrs199473199
googlers199473199
pharmgkbrs199473199
gwascentralrs199473199
openSNPrs199473199
23andMers199473199
23andMe allrs199473199
SNP Nexus

SNPshotrs199473199
SNPdbers199473199
MSV3drs199473199
GWAS Ctlgrs199473199
Max Magnitude0
ClinVar
Risk rs199473199(C;C)
Alt rs199473199(C;C)
Reference rs199473199(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38618244C>G
CLNSRC ClinVar
CLNACC RCV000058571.2,