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rs199473592

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473592(A;A)
Make rs199473592(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581091
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473592
ebirs199473592
HLIrs199473592
Exacrs199473592
Varsomers199473592
Maprs199473592
PheGenIrs199473592
hapmaprs199473592
1000 genomesrs199473592
hgdprs199473592
ensemblrs199473592
gopubmedrs199473592
geneviewrs199473592
scholarrs199473592
googlers199473592
pharmgkbrs199473592
gwascentralrs199473592
openSNPrs199473592
23andMers199473592
23andMe allrs199473592
SNP Nexus

SNPshotrs199473592
SNPdbers199473592
MSV3drs199473592
GWAS Ctlgrs199473592
Max Magnitude0
ClinVar
Risk rs199473592(A,C;A,C)
Alt rs199473592(A,C;A,C)
Reference rs199473592(G;G)
Significance Other
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38622582C>T
CLNSRC ClinVar
CLNACC RCV000058546.3, RCV000183023.2,