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rs397514446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514446(-;-)
Make rs397514446(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position38560202
GeneSCN5A
is asnp
is mentioned by
dbSNPrs397514446
ebirs397514446
HLIrs397514446
Exacrs397514446
Varsomers397514446
Maprs397514446
PheGenIrs397514446
hapmaprs397514446
1000 genomesrs397514446
hgdprs397514446
ensemblrs397514446
gopubmedrs397514446
geneviewrs397514446
scholarrs397514446
googlers397514446
pharmgkbrs397514446
gwascentralrs397514446
openSNPrs397514446
23andMers397514446
23andMe allrs397514446
SNP Nexus

SNPshotrs397514446
SNPdbers397514446
MSV3drs397514446
GWAS Ctlgrs397514446
Max Magnitude0
ClinVar
Risk rs397514446(;)
Alt rs397514446(;)
Reference rs397514446(A;A)
Significance Pathogenic
Disease Brugada syndrome 1
Variation info
Gene SCN5A
CLNDBN Brugada syndrome 1
Reversed 1
HGVS NC_000003.11:g.38601693delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000009967.2,