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rs883079

From SNPedia

Orientationminus
Stabilizedminus
Make rs883079(A;A)
Make rs883079(A;G)
Make rs883079(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114355435
GeneTBX5
is asnp
is mentioned by
dbSNPrs883079
ClinGenrs883079
ebirs883079
HLIrs883079
Exacrs883079
Varsomers883079
Maprs883079
PheGenIrs883079
hapmaprs883079
1000 genomesrs883079
hgdprs883079
ensemblrs883079
gopubmedrs883079
geneviewrs883079
scholarrs883079
googlers883079
pharmgkbrs883079
gwascentralrs883079
openSNPrs883079
23andMers883079
23andMe allrs883079
SNP Nexus

SNPshotrs883079
SNPdbers883079
MSV3drs883079
GWAS Ctlgrs883079
GMAF0.3949
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele C
P-val 1E-10
Odds Ratio 0.4900 [0.33-0.65] ms increase


[PMID 27479212OA-icon.png] Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.


ClinVar
Risk rs883079(A;A) rs883079(C;C)
Alt rs883079(A;A) rs883079(C;C)
Reference rs883079(G;G)
Significance Non-pathogenic
Disease Holt-Oram syndrome
Variation info
Gene TBX5
CLNDBN Holt-Oram syndrome
Reversed 1
HGVS NC_000012.11:g.114793240C>T
CLNSRC
CLNACC RCV000383069.1,