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rs199473225

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473225(C;T)
Make rs199473225(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560397
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473225
ebirs199473225
HLIrs199473225
Exacrs199473225
Varsomers199473225
Maprs199473225
PheGenIrs199473225
hapmaprs199473225
1000 genomesrs199473225
hgdprs199473225
ensemblrs199473225
gopubmedrs199473225
geneviewrs199473225
scholarrs199473225
googlers199473225
pharmgkbrs199473225
gwascentralrs199473225
openSNPrs199473225
23andMers199473225
23andMe allrs199473225
SNP Nexus

SNPshotrs199473225
SNPdbers199473225
MSV3drs199473225
GWAS Ctlgrs199473225
Max Magnitude0
ClinVar
Risk rs199473225(G,T;G,T)
Alt rs199473225(G,T;G,T)
Reference rs199473225(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.38601888G>A; NC_000003.11:g.38601888G>C
CLNSRC ClinVar
CLNACC RCV000058623.2, RCV000183056.1, RCV000183055.2,