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rs199473577

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473577(C;T)
Make rs199473577(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38603744
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473577
ebirs199473577
HLIrs199473577
Exacrs199473577
Varsomers199473577
Maprs199473577
PheGenIrs199473577
hapmaprs199473577
1000 genomesrs199473577
hgdprs199473577
ensemblrs199473577
gopubmedrs199473577
geneviewrs199473577
scholarrs199473577
googlers199473577
pharmgkbrs199473577
gwascentralrs199473577
openSNPrs199473577
23andMers199473577
23andMe allrs199473577
SNP Nexus

SNPshotrs199473577
SNPdbers199473577
MSV3drs199473577
GWAS Ctlgrs199473577
Max Magnitude0
ClinVar
Risk rs199473577(T;T)
Alt rs199473577(T;T)
Reference rs199473577(C;C)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38645235G>A
CLNSRC ClinVar
CLNACC RCV000058458.2,