Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473217(C;G)
Make rs199473217(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38562515
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473217
ebirs199473217
HLIrs199473217
Exacrs199473217
Varsomers199473217
Maprs199473217
PheGenIrs199473217
hapmaprs199473217
1000 genomesrs199473217
hgdprs199473217
ensemblrs199473217
gopubmedrs199473217
geneviewrs199473217
scholarrs199473217
googlers199473217
pharmgkbrs199473217
gwascentralrs199473217
openSNPrs199473217
23andMers199473217
23andMe allrs199473217
SNP Nexus

SNPshotrs199473217
SNPdbers199473217
MSV3drs199473217
GWAS Ctlgrs199473217
Max Magnitude0
ClinVar
Risk rs199473217(G;G)
Alt rs199473217(G;G)
Reference rs199473217(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38604006G>C
CLNSRC ClinVar
CLNACC RCV000058609.2,