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

rs727503411

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503411(-;-)
Make rs727503411(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38633053
GeneSCN5A
is asnp
is mentioned by
dbSNPrs727503411
ebirs727503411
HLIrs727503411
Exacrs727503411
Varsomers727503411
Maprs727503411
PheGenIrs727503411
hapmaprs727503411
1000 genomesrs727503411
hgdprs727503411
ensemblrs727503411
gopubmedrs727503411
geneviewrs727503411
scholarrs727503411
googlers727503411
pharmgkbrs727503411
gwascentralrs727503411
openSNPrs727503411
23andMers727503411
23andMe allrs727503411
SNP Nexus

SNPshotrs727503411
SNPdbers727503411
MSV3drs727503411
GWAS Ctlgrs727503411
Max Magnitude0
ClinVar
Risk rs727503411(;)
Alt rs727503411(;)
Reference rs727503411(C;C)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38674544delG
CLNSRC
CLNACC RCV000151808.1,