Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473144

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473144(G;G)
Make rs199473144(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38597944
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473144
ebirs199473144
HLIrs199473144
Exacrs199473144
Varsomers199473144
Maprs199473144
PheGenIrs199473144
hapmaprs199473144
1000 genomesrs199473144
hgdprs199473144
ensemblrs199473144
gopubmedrs199473144
geneviewrs199473144
scholarrs199473144
googlers199473144
pharmgkbrs199473144
gwascentralrs199473144
openSNPrs199473144
23andMers199473144
23andMe allrs199473144
SNP Nexus

SNPshotrs199473144
SNPdbers199473144
MSV3drs199473144
GWAS Ctlgrs199473144
Max Magnitude0
ClinVar
Risk rs199473144(C,G;C,G)
Alt rs199473144(C,G;C,G)
Reference rs199473144(T;T)
Significance Pathogenic
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38639435A>C; NC_000003.11:g.38639435A>G
CLNSRC ClinVar
CLNACC RCV000058475.2, RCV000182994.2,