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rs886037903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs886037903(-;-)
Make rs886037903(-;CT)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position38551015
GeneSCN5A
is asnp
is mentioned by
dbSNPrs886037903
dbSNP (classic)rs886037903
ClinGenrs886037903
ebirs886037903
HLIrs886037903
Exacrs886037903
Gnomadrs886037903
Varsomers886037903
LitVarrs886037903
Maprs886037903
PheGenIrs886037903
Biobankrs886037903
1000 genomesrs886037903
hgdprs886037903
ensemblrs886037903
geneviewrs886037903
scholarrs886037903
googlers886037903
pharmgkbrs886037903
gwascentralrs886037903
openSNPrs886037903
23andMers886037903
23andMe allrs886037903
SNPshotrs886037903
SNPdbers886037903
MSV3drs886037903
GWAS Ctlgrs886037903
Max Magnitude0
ClinVar
Risk rs886037903(-;-)
Alt rs886037903(-;-)
Reference Rs886037903(CT;CT)
Significance Probable-Pathogenic
Disease Brugada syndrome 1
Variation info
Gene SCN5A
CLNDBN Brugada syndrome 1
Reversed 1
HGVS NC_000003.11:g.38592506_38592507delAG
CLNSRC
CLNACC RCV000240623.1,