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rs267607029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607029(A;A)
Make rs267607029(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35033828
GeneSCN1B
is asnp
is mentioned by
dbSNPrs267607029
ebirs267607029
HLIrs267607029
Exacrs267607029
Varsomers267607029
Maprs267607029
PheGenIrs267607029
hapmaprs267607029
1000 genomesrs267607029
hgdprs267607029
ensemblrs267607029
gopubmedrs267607029
geneviewrs267607029
scholarrs267607029
googlers267607029
pharmgkbrs267607029
gwascentralrs267607029
openSNPrs267607029
23andMers267607029
23andMe allrs267607029
SNP Nexus

SNPshotrs267607029
SNPdbers267607029
MSV3drs267607029
GWAS Ctlgrs267607029
Max Magnitude0
ClinVar
Risk rs267607029(A;A)
Alt rs267607029(A;A)
Reference rs267607029(G;G)
Significance Pathogenic
Disease Cardiac conduction defect
Variation info
Gene SCN1B
CLNDBN Cardiac conduction defect, nonspecific
Reversed 0
HGVS NC_000019.9:g.35524732G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009838.2,