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rs199473172

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473172(A;A)
Make rs199473172(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585800
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473172
ebirs199473172
HLIrs199473172
Exacrs199473172
Varsomers199473172
Maprs199473172
PheGenIrs199473172
hapmaprs199473172
1000 genomesrs199473172
hgdprs199473172
ensemblrs199473172
gopubmedrs199473172
geneviewrs199473172
scholarrs199473172
googlers199473172
pharmgkbrs199473172
gwascentralrs199473172
openSNPrs199473172
23andMers199473172
23andMe allrs199473172
SNP Nexus

SNPshotrs199473172
SNPdbers199473172
MSV3drs199473172
GWAS Ctlgrs199473172
Max Magnitude0
ClinVar
Risk rs199473172(A,T;A,T)
Alt rs199473172(A,T;A,T)
Reference rs199473172(G;G)
Significance Pathogenic
Disease not provided Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not provided Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627291C>A; NC_000003.11:g.38627291C>T
CLNSRC ClinVar
CLNACC RCV000183179.1, RCV000058518.2,