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rs185492581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs185492581(C;C)
Make rs185492581(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38630327
GeneSCN5A
is asnp
is mentioned by
dbSNPrs185492581
ebirs185492581
HLIrs185492581
Exacrs185492581
Varsomers185492581
Maprs185492581
PheGenIrs185492581
hapmaprs185492581
1000 genomesrs185492581
hgdprs185492581
ensemblrs185492581
gopubmedrs185492581
geneviewrs185492581
scholarrs185492581
googlers185492581
pharmgkbrs185492581
gwascentralrs185492581
openSNPrs185492581
23andMers185492581
23andMe allrs185492581
SNP Nexus

SNPshotrs185492581
SNPdbers185492581
MSV3drs185492581
GWAS Ctlgrs185492581
Max Magnitude0
ClinVar
Risk rs185492581(C;C)
Alt rs185492581(C;C)
Reference rs185492581(T;T)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38671818T>C
CLNSRC ClinVar
CLNACC RCV000058601.2,