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rs199473573

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473573(G;G)
Make rs199473573(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38604007
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473573
ebirs199473573
HLIrs199473573
Exacrs199473573
Varsomers199473573
Maprs199473573
PheGenIrs199473573
hapmaprs199473573
1000 genomesrs199473573
hgdprs199473573
ensemblrs199473573
gopubmedrs199473573
geneviewrs199473573
scholarrs199473573
googlers199473573
pharmgkbrs199473573
gwascentralrs199473573
openSNPrs199473573
23andMers199473573
23andMe allrs199473573
SNP Nexus

SNPshotrs199473573
SNPdbers199473573
MSV3drs199473573
GWAS Ctlgrs199473573
Max Magnitude0
ClinVar
Risk rs199473573(G;G)
Alt rs199473573(G;G)
Reference rs199473573(T;T)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38645498A>C
CLNSRC ClinVar
CLNACC RCV000058434.2, RCV000182979.2,