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rs3807375

From SNPedia

Orientationminus
Stabilizedminus
Make rs3807375(A;A)
Make rs3807375(A;G)
Make rs3807375(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150970122
GeneKCNH2
is asnp
is mentioned by
dbSNPrs3807375
ebirs3807375
HLIrs3807375
Exacrs3807375
Varsomers3807375
Maprs3807375
PheGenIrs3807375
hapmaprs3807375
1000 genomesrs3807375
hgdprs3807375
ensemblrs3807375
gopubmedrs3807375
geneviewrs3807375
scholarrs3807375
googlers3807375
pharmgkbrs3807375
gwascentralrs3807375
openSNPrs3807375
23andMers3807375
23andMe allrs3807375
SNP Nexus

SNPshotrs3807375
SNPdbers3807375
MSV3drs3807375
GWAS Ctlgrs3807375
GMAF0.4219
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19019189OA-icon.png] QT interval rs3807375 rs2880058


GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele T
P-val 5E-11
Odds Ratio 11.95 [8.39-15.51] % SD increase


[PMID 20215044OA-icon.png] Relationship of Common Candidate Gene Variants to Electrocardiographic T-Wave Peak to T-Wave End Interval and T-Wave Morphology Parameters



[PMID 19214780OA-icon.png] In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).


[PMID 19305408OA-icon.png] Common variants at ten loci influence QT interval duration in the QTGEN Study.


[PMID 19490382] Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese.


GET Evidence
rs3807375
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.531746
summary