Have questions? Visit https://www.reddit.com/r/SNPedia

rs452036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs452036(A;A)
Make rs452036(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23396676
GeneMYH6
is asnp
is mentioned by
dbSNPrs452036
dbSNP (old)rs452036
ClinGenrs452036
ebirs452036
HLIrs452036
Exacrs452036
Gnomadrs452036
Varsomers452036
Maprs452036
PheGenIrs452036
Biobankrs452036
1000 genomesrs452036
hgdprs452036
ensemblrs452036
gopubmedrs452036
geneviewrs452036
scholarrs452036
googlers452036
pharmgkbrs452036
gwascentralrs452036
openSNPrs452036
23andMers452036
23andMe allrs452036
SNP Nexus

SNPshotrs452036
SNPdbers452036
MSV3drs452036
GWAS Ctlgrs452036
GMAF0.3522
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20639392OA-icon.png]
Trait Resting heart rate
Title Genome-wide association analysis identifies multiple loci related with resting heart rate
Risk Allele A
P-val 4E-14
Odds Ratio 7.80 [5.84-9.76] ms decrease
GWAS snp
PMID [PMID 23183192OA-icon.png]
Trait Resting heart rate
Title Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: A genome-wide association study of 13,372 participants.
Risk Allele G
P-val 8E-7
Odds Ratio 9.60 [5.68-13.52] ms increase


ClinVar
Risk rs452036(A;A)
Alt rs452036(A;A)
Reference Rs452036(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MYH6
CLNDBN not specified
Reversed 0
HGVS NC_000014.8:g.23865885G>A
CLNSRC
CLNACC RCV000242804.1,