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rs199473565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473565(A;A)
Make rs199473565(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606743
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473565
ebirs199473565
HLIrs199473565
Exacrs199473565
Varsomers199473565
Maprs199473565
PheGenIrs199473565
hapmaprs199473565
1000 genomesrs199473565
hgdprs199473565
ensemblrs199473565
gopubmedrs199473565
geneviewrs199473565
scholarrs199473565
googlers199473565
pharmgkbrs199473565
gwascentralrs199473565
openSNPrs199473565
23andMers199473565
23andMe allrs199473565
SNP Nexus

SNPshotrs199473565
SNPdbers199473565
MSV3drs199473565
GWAS Ctlgrs199473565
Max Magnitude0
ClinVar
Risk rs199473565(A;A)
Alt rs199473565(A;A)
Reference rs199473565(G;G)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38648234C>T
CLNSRC ClinVar
CLNACC RCV000058388.2, RCV000182956.2,