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rs869025522

From SNPedia

Orientationminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs869025522(-;-)
Make rs869025522(-;AAG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38555719
GeneSCN5A
is asnp
is mentioned by
dbSNPrs869025522
ebirs869025522
HLIrs869025522
Exacrs869025522
Varsomers869025522
Maprs869025522
PheGenIrs869025522
hapmaprs869025522
1000 genomesrs869025522
hgdprs869025522
ensemblrs869025522
gopubmedrs869025522
geneviewrs869025522
scholarrs869025522
googlers869025522
pharmgkbrs869025522
gwascentralrs869025522
openSNPrs869025522
23andMers869025522
23andMe allrs869025522
SNP Nexus

SNPshotrs869025522
SNPdbers869025522
MSV3drs869025522
GWAS Ctlgrs869025522
Max Magnitude0
ClinVar
Risk rs869025522(;)
Alt rs869025522(;)
Reference rs869025522(AAG;AAG)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38597210_38597212delCTT
CLNSRC
CLNACC RCV000208493.1,