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

rs886037904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886037904(-;GGGT)
Make rs886037904(GGGT;GGGT)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position38554272
GeneSCN5A
is asnp
is mentioned by
dbSNPrs886037904
dbSNP (classic)rs886037904
ClinGenrs886037904
ebirs886037904
HLIrs886037904
Exacrs886037904
Gnomadrs886037904
Varsomers886037904
LitVarrs886037904
Maprs886037904
PheGenIrs886037904
Biobankrs886037904
1000 genomesrs886037904
hgdprs886037904
ensemblrs886037904
geneviewrs886037904
scholarrs886037904
googlers886037904
pharmgkbrs886037904
gwascentralrs886037904
openSNPrs886037904
23andMers886037904
23andMe allrs886037904
SNPshotrs886037904
SNPdbers886037904
MSV3drs886037904
GWAS Ctlgrs886037904
Max Magnitude0
ClinVar
Risk rs886037904(GGGT;GGGT)
Alt rs886037904(GGGT;GGGT)
Reference Rs886037904(-;-)
Significance Probable-Pathogenic
Disease Brugada syndrome 1
Variation info
Gene SCN5A
CLNDBN Brugada syndrome 1
Reversed 1
HGVS NC_000003.11:g.38595764_38595767dupACCC
CLNSRC
CLNACC RCV000240648.1,