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rs727505158

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727505158(-;-)
Make rs727505158(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38599005
GeneSCN5A
is asnp
is mentioned by
dbSNPrs727505158
ebirs727505158
HLIrs727505158
Exacrs727505158
Varsomers727505158
Maprs727505158
PheGenIrs727505158
hapmaprs727505158
1000 genomesrs727505158
hgdprs727505158
ensemblrs727505158
gopubmedrs727505158
geneviewrs727505158
scholarrs727505158
googlers727505158
pharmgkbrs727505158
gwascentralrs727505158
openSNPrs727505158
23andMers727505158
23andMe allrs727505158
SNP Nexus

SNPshotrs727505158
SNPdbers727505158
MSV3drs727505158
GWAS Ctlgrs727505158
Max Magnitude0
ClinVar
Risk rs727505158(;)
Alt rs727505158(;)
Reference rs727505158(C;C)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38640496delG
CLNSRC
CLNACC RCV000156628.3, RCV000183151.2,