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rs199473292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473292(C;C)
Make rs199473292(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551391
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473292
ebirs199473292
HLIrs199473292
Exacrs199473292
Varsomers199473292
Maprs199473292
PheGenIrs199473292
hapmaprs199473292
1000 genomesrs199473292
hgdprs199473292
ensemblrs199473292
gopubmedrs199473292
geneviewrs199473292
scholarrs199473292
googlers199473292
pharmgkbrs199473292
gwascentralrs199473292
openSNPrs199473292
23andMers199473292
23andMe allrs199473292
SNP Nexus

SNPshotrs199473292
SNPdbers199473292
MSV3drs199473292
GWAS Ctlgrs199473292
Max Magnitude0
ClinVar
Risk rs199473292(A,C;A,C)
Alt rs199473292(A,C;A,C)
Reference rs199473292(G;G)
Significance Pathogenic
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38592882C>G; NC_000003.11:g.38592882C>T
CLNSRC ClinVar
CLNACC RCV000058733.2, RCV000183094.2,