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rs199473076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473076(A;A)
Make rs199473076(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609950
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473076
ebirs199473076
HLIrs199473076
Exacrs199473076
Varsomers199473076
Maprs199473076
PheGenIrs199473076
hapmaprs199473076
1000 genomesrs199473076
hgdprs199473076
ensemblrs199473076
gopubmedrs199473076
geneviewrs199473076
scholarrs199473076
googlers199473076
pharmgkbrs199473076
gwascentralrs199473076
openSNPrs199473076
23andMers199473076
23andMe allrs199473076
SNP Nexus

SNPshotrs199473076
SNPdbers199473076
MSV3drs199473076
GWAS Ctlgrs199473076
Max Magnitude0
ClinVar
Risk rs199473076(A;A)
Alt rs199473076(A;A)
Reference rs199473076(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.38651441C>T
CLNSRC ClinVar
CLNACC RCV000058842.2, RCV000182946.2,