Rs4657139

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs4657139
hapmaprs4657139
hgdprs4657139
ensemblrs4657139
gopubmedrs4657139
scholarrs4657139
googlers4657139
pharmgkbrs4657139
hgvbaseg2prs4657139
medrefsnprs4657139
23andMers4657139
SNP Nexus

Chromosome1
Orientationplus
Position160296530
GenotypeEffect
rs4657139(A;A)*?
rs4657139(A;T)*?
rs4657139(T;T)*?


[PMID 19204306] rs10494366, rs4657139 and rs16847548 were significantly associated with adjusted QT interval in whites. relative hazard of SCD associated with each C allele at rs16847548 was 1.31. rs12567209 was also independently associated with SCD in whites (relative hazard 0.57, 95% confidence interval 0.39 to 0.83, P=0.003). No significant associations observed in blacks.
? (A;A) (A;T) (T;T)


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