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rs879253730

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253730(C;G)
Make rs879253730(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position123642468
GeneSCN3B
is asnp
is mentioned by
dbSNPrs879253730
ebirs879253730
HLIrs879253730
Exacrs879253730
Varsomers879253730
Maprs879253730
PheGenIrs879253730
hapmaprs879253730
1000 genomesrs879253730
hgdprs879253730
ensemblrs879253730
gopubmedrs879253730
geneviewrs879253730
scholarrs879253730
googlers879253730
pharmgkbrs879253730
gwascentralrs879253730
openSNPrs879253730
23andMers879253730
23andMe allrs879253730
SNP Nexus

SNPshotrs879253730
SNPdbers879253730
MSV3drs879253730
GWAS Ctlgrs879253730
Max Magnitude0
ClinVar
Risk rs879253730(G;G)
Alt rs879253730(G;G)
Reference rs879253730(C;C)
Significance Pathogenic
Disease Arrhythmia
Variation info
Gene SCN3B
CLNDBN Arrhythmia
Reversed 1
HGVS NC_000011.9:g.123513176G>C
CLNSRC
CLNACC RCV000234971.1,