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rs193922728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922728(A;A)
Make rs193922728(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35034042
GeneSCN1B
is asnp
is mentioned by
dbSNPrs193922728
ebirs193922728
HLIrs193922728
Exacrs193922728
Varsomers193922728
Maprs193922728
PheGenIrs193922728
hapmaprs193922728
1000 genomesrs193922728
hgdprs193922728
ensemblrs193922728
gopubmedrs193922728
geneviewrs193922728
scholarrs193922728
googlers193922728
pharmgkbrs193922728
gwascentralrs193922728
openSNPrs193922728
23andMers193922728
23andMe allrs193922728
SNP Nexus

SNPshotrs193922728
SNPdbers193922728
MSV3drs193922728
GWAS Ctlgrs193922728
Max Magnitude0
ClinVar
Risk rs193922728(A;A)
Alt rs193922728(A;A)
Reference rs193922728(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene SCN1B
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000019.9:g.35524946G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030436.1,