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

rs199473612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473612(C;T)
Make rs199473612(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38557247
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473612
dbSNP (classic)rs199473612
ClinGenrs199473612
ebirs199473612
HLIrs199473612
Exacrs199473612
Gnomadrs199473612
Varsomers199473612
LitVarrs199473612
Maprs199473612
PheGenIrs199473612
Biobankrs199473612
1000 genomesrs199473612
hgdprs199473612
ensemblrs199473612
geneviewrs199473612
scholarrs199473612
googlers199473612
pharmgkbrs199473612
gwascentralrs199473612
openSNPrs199473612
23andMers199473612
SNPshotrs199473612
SNPdbers199473612
MSV3drs199473612
GWAS Ctlgrs199473612
Max Magnitude0
ClinVar
Risk rs199473612(T;T)
Alt rs199473612(T;T)
Reference Rs199473612(C;C)
Significance Untested
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38598738G>A
CLNSRC ClinVar
CLNACC RCV000058656.2,