rs883079

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs883079(A;A)

Make rs883079(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

114355435

Gene

TBX5

is a	snp
is	mentioned by
dbSNP	rs883079
dbSNP (classic)	rs883079
ClinGen	rs883079
ebi	rs883079
HLI	rs883079
Exac	rs883079
Gnomad	rs883079
Varsome	rs883079
LitVar	rs883079
Map	rs883079
PheGenI	rs883079
Biobank	rs883079
1000 genomes	rs883079
hgdp	rs883079
ensembl	rs883079
geneview	rs883079
scholar	rs883079
google	rs883079
pharmgkb	rs883079
gwascentral	rs883079
openSNP	rs883079
23andMe	rs883079
SNPshot	rs883079
SNPdbe	rs883079
MSV3d	rs883079
GWAS Ctlg	rs883079

GMAF

0.3949

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 21076409]
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 27479212] 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,