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rs199473171

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473171(C;T)
Make rs199473171(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585801
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473171
ebirs199473171
HLIrs199473171
Exacrs199473171
Varsomers199473171
Maprs199473171
PheGenIrs199473171
hapmaprs199473171
1000 genomesrs199473171
hgdprs199473171
ensemblrs199473171
gopubmedrs199473171
geneviewrs199473171
scholarrs199473171
googlers199473171
pharmgkbrs199473171
gwascentralrs199473171
openSNPrs199473171
23andMers199473171
23andMe allrs199473171
SNP Nexus

SNPshotrs199473171
SNPdbers199473171
MSV3drs199473171
GWAS Ctlgrs199473171
Max Magnitude0
ClinVar
Risk rs199473171(T;T)
Alt rs199473171(T;T)
Reference rs199473171(C;C)
Significance Pathogenic
Disease Brugada syndrome not specified
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38627292G>A
CLNSRC ClinVar
CLNACC RCV000058517.2, RCV000183009.2,