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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
dbSNP (classic)rs185492581
ClinGenrs185492581
ebirs185492581
HLIrs185492581
Exacrs185492581
Gnomadrs185492581
Varsomers185492581
LitVarrs185492581
Maprs185492581
PheGenIrs185492581
Biobankrs185492581
1000 genomesrs185492581
hgdprs185492581
ensemblrs185492581
geneviewrs185492581
scholarrs185492581
googlers185492581
pharmgkbrs185492581
gwascentralrs185492581
openSNPrs185492581
23andMers185492581
SNPshotrs185492581
SNPdbers185492581
MSV3drs185492581
GWAS Ctlgrs185492581
Max Magnitude0
ClinVar
Risk rs185492581(C;C)
Alt rs185492581(C;C)
Reference Rs185492581(T;T)
Significance Untested
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38671818T>C
CLNSRC UniProtKB (protein)
CLNACC RCV000058601.2,