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rs727505158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;C) 6 Brugada Syndrome
(C;C) 0 common in clinvar


Make rs727505158(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38599005
GeneSCN5A
is asnp
is mentioned by
dbSNPrs727505158
dbSNP (classic)rs727505158
ClinGenrs727505158
ebirs727505158
HLIrs727505158
Exacrs727505158
Gnomadrs727505158
Varsomers727505158
LitVarrs727505158
Maprs727505158
PheGenIrs727505158
Biobankrs727505158
1000 genomesrs727505158
hgdprs727505158
ensemblrs727505158
geneviewrs727505158
scholarrs727505158
googlers727505158
pharmgkbrs727505158
gwascentralrs727505158
openSNPrs727505158
23andMers727505158
SNPshotrs727505158
SNPdbers727505158
MSV3drs727505158
GWAS Ctlgrs727505158
Max Magnitude6
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 RCV000156628.4, RCV000183151.4,