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rs16969925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs16969925(A;A)
Make rs16969925(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35033545
GeneSCN1B
is asnp
is mentioned by
dbSNPrs16969925
ebirs16969925
HLIrs16969925
Exacrs16969925
Varsomers16969925
Maprs16969925
PheGenIrs16969925
hapmaprs16969925
1000 genomesrs16969925
hgdprs16969925
ensemblrs16969925
gopubmedrs16969925
geneviewrs16969925
scholarrs16969925
googlers16969925
pharmgkbrs16969925
gwascentralrs16969925
openSNPrs16969925
23andMers16969925
23andMe allrs16969925
SNP Nexus

SNPshotrs16969925
SNPdbers16969925
MSV3drs16969925
GWAS Ctlgrs16969925
Max Magnitude0
ClinVar
Risk rs16969925(A;A)
Alt rs16969925(A;A)
Reference rs16969925(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN1B
CLNDBN Atrial fibrillation, familial, 13
Reversed 0
HGVS NC_000019.9:g.35524449G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054537.2,