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

rs199473176

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473176(G;G)
Make rs199473176(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585728
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473176
ebirs199473176
HLIrs199473176
Exacrs199473176
Varsomers199473176
Maprs199473176
PheGenIrs199473176
hapmaprs199473176
1000 genomesrs199473176
hgdprs199473176
ensemblrs199473176
gopubmedrs199473176
geneviewrs199473176
scholarrs199473176
googlers199473176
pharmgkbrs199473176
gwascentralrs199473176
openSNPrs199473176
23andMers199473176
23andMe allrs199473176
SNP Nexus

SNPshotrs199473176
SNPdbers199473176
MSV3drs199473176
GWAS Ctlgrs199473176
Max Magnitude0
ClinVar
Risk rs199473176(G;G)
Alt rs199473176(G;G)
Reference rs199473176(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627219A>C
CLNSRC ClinVar
CLNACC RCV000058524.2,