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rs869025520

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025520(C;T)
Make rs869025520(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38579372
GeneSCN5A
is asnp
is mentioned by
dbSNPrs869025520
ebirs869025520
HLIrs869025520
Exacrs869025520
Varsomers869025520
Maprs869025520
PheGenIrs869025520
hapmaprs869025520
1000 genomesrs869025520
hgdprs869025520
ensemblrs869025520
gopubmedrs869025520
geneviewrs869025520
scholarrs869025520
googlers869025520
pharmgkbrs869025520
gwascentralrs869025520
openSNPrs869025520
23andMers869025520
23andMe allrs869025520
SNP Nexus

SNPshotrs869025520
SNPdbers869025520
MSV3drs869025520
GWAS Ctlgrs869025520
Max Magnitude0
ClinVar
Risk rs869025520(T;T)
Alt rs869025520(T;T)
Reference rs869025520(C;C)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38620863G>A
CLNSRC
CLNACC RCV000208454.1, RCV000213225.1,