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rs121918282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918282(C;C)
Make rs121918282(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position123653773
GeneSCN3B
is asnp
is mentioned by
dbSNPrs121918282
ebirs121918282
HLIrs121918282
Exacrs121918282
Varsomers121918282
Maprs121918282
PheGenIrs121918282
hapmaprs121918282
1000 genomesrs121918282
hgdprs121918282
ensemblrs121918282
gopubmedrs121918282
geneviewrs121918282
scholarrs121918282
googlers121918282
pharmgkbrs121918282
gwascentralrs121918282
openSNPrs121918282
23andMers121918282
23andMe allrs121918282
SNP Nexus

SNPshotrs121918282
SNPdbers121918282
MSV3drs121918282
GWAS Ctlgrs121918282
Max Magnitude0
OMIM608214
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918282(C;C)
Alt rs121918282(C;C)
Reference rs121918282(T;T)
Significance Pathogenic
Disease Brugada syndrome 7 Atrial fibrillation not provided Brugada syndrome not specified
Variation info
Gene SCN3B
CLNDBN Brugada syndrome 7 Atrial fibrillation, familial, 16 not provided Brugada syndrome not specified
Reversed 1
HGVS NC_000011.9:g.123524481A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002574.8, RCV000128811.5, RCV000171069.4, RCV000171567.1, RCV000220802.1,