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rs267607028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607028(A;A)
Make rs267607028(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35033827
GeneSCN1B
is asnp
is mentioned by
dbSNPrs267607028
ebirs267607028
HLIrs267607028
Exacrs267607028
Varsomers267607028
Maprs267607028
PheGenIrs267607028
hapmaprs267607028
1000 genomesrs267607028
hgdprs267607028
ensemblrs267607028
gopubmedrs267607028
geneviewrs267607028
scholarrs267607028
googlers267607028
pharmgkbrs267607028
gwascentralrs267607028
openSNPrs267607028
23andMers267607028
23andMe allrs267607028
SNP Nexus

SNPshotrs267607028
SNPdbers267607028
MSV3drs267607028
GWAS Ctlgrs267607028
Max Magnitude0
ClinVar
Risk rs267607028(A;A)
Alt rs267607028(A;A)
Reference rs267607028(G;G)
Significance Pathogenic
Disease Brugada syndrome 5 not provided
Variation info
Gene SCN1B
CLNDBN Brugada syndrome 5 not provided
Reversed 0
HGVS NC_000019.9:g.35524731G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009836.4, RCV000171062.2,