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rs17121819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17121819(C;T)
Make rs17121819(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position118168740
GeneSCN2B
is asnp
is mentioned by
dbSNPrs17121819
ebirs17121819
HLIrs17121819
Exacrs17121819
Varsomers17121819
Maprs17121819
PheGenIrs17121819
hapmaprs17121819
1000 genomesrs17121819
hgdprs17121819
ensemblrs17121819
gopubmedrs17121819
geneviewrs17121819
scholarrs17121819
googlers17121819
pharmgkbrs17121819
gwascentralrs17121819
openSNPrs17121819
23andMers17121819
23andMe allrs17121819
SNP Nexus

SNPshotrs17121819
SNPdbers17121819
MSV3drs17121819
GWAS Ctlgrs17121819
Max Magnitude0
ClinVar
Risk rs17121819(T;T)
Alt rs17121819(T;T)
Reference rs17121819(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN2B
CLNDBN Atrial fibrillation, familial, 14
Reversed 1
HGVS NC_000011.9:g.118039455G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054539.2,