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rs199473613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473613(A;G)
Make rs199473613(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38556532
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473613
ebirs199473613
HLIrs199473613
Exacrs199473613
Varsomers199473613
Maprs199473613
PheGenIrs199473613
hapmaprs199473613
1000 genomesrs199473613
hgdprs199473613
ensemblrs199473613
gopubmedrs199473613
geneviewrs199473613
scholarrs199473613
googlers199473613
pharmgkbrs199473613
gwascentralrs199473613
openSNPrs199473613
23andMers199473613
23andMe allrs199473613
SNP Nexus

SNPshotrs199473613
SNPdbers199473613
MSV3drs199473613
GWAS Ctlgrs199473613
Max Magnitude0
ClinVar
Risk rs199473613(G;G)
Alt rs199473613(G;G)
Reference rs199473613(A;A)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38598023T>C
CLNSRC ClinVar
CLNACC RCV000058664.2, RCV000183070.1,