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rs387906805

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906805(C;T)
Make rs387906805(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position21805184
GeneABCC9
is asnp
is mentioned by
dbSNPrs387906805
ebirs387906805
HLIrs387906805
Exacrs387906805
Varsomers387906805
Maprs387906805
PheGenIrs387906805
hapmaprs387906805
1000 genomesrs387906805
hgdprs387906805
ensemblrs387906805
gopubmedrs387906805
geneviewrs387906805
scholarrs387906805
googlers387906805
pharmgkbrs387906805
gwascentralrs387906805
openSNPrs387906805
23andMers387906805
23andMe allrs387906805
SNP Nexus

SNPshotrs387906805
SNPdbers387906805
MSV3drs387906805
GWAS Ctlgrs387906805
Max Magnitude0
ClinVar
Risk rs387906805(T;T)
Alt rs387906805(T;T)
Reference rs387906805(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene ABCC9
CLNDBN Atrial fibrillation, familial, 12
Reversed 1
HGVS NC_000012.11:g.21958118G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023103.3,