Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population

Pulse rate is known to be related to diverse phenotypes, such as cardiovascular diseases, lifespan, arrhythmia, hypertension, lipids, diabetes, and menopause. We have reported two genomewide significant genetic loci responsible for the variation in pulse rate as a part of the Korea Association Resou...

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Published inGenomics & informatics Vol. 10; no. 2; pp. 106 - 109
Main Authors Kim, Nam Hee, Kim, Young Jin, Oh, Ji Hee, Cho, Yoon Shin
Format Journal Article
LanguageEnglish
Published Korea (South) Korea Genome Organization 01.06.2012
한국유전체학회
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Summary:Pulse rate is known to be related to diverse phenotypes, such as cardiovascular diseases, lifespan, arrhythmia, hypertension, lipids, diabetes, and menopause. We have reported two genomewide significant genetic loci responsible for the variation in pulse rate as a part of the Korea Association Resource (KARE) project, the genomewide association study (GWAS) that was conducted with 352,228 single nucleoride polymorphisms typed in 8,842 subjects in the Korean population. GJA1 was implied as a functionally causal gene for pulse rate from the KARE study, but lacked evidence of replication. To re-evaluate the association of a locus near GJA1 with pulse rate, we looked up this signal in another GWAS conducted in a Health Examinee-shared cohort of 3,703 samples. Not only we were able to confirm two pulse rate loci (1q32.2a near CD46 and 6q22.13c near LOCL644502) identified in the KARE GWAS, we also replicated a locus (6q22.31c) near GJA1 by the lookup in the Health Examinee GWAS. Considering that the GJA1-encoded protein is a major component of cardiac gap junctions, a functional study might be necessary to validate its genuine molecular biological role in the synchronized contraction of the heart.
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G704-001931.2012.10.2.010
ISSN:1598-866X
2234-0742
2234-0742
DOI:10.5808/GI.2012.10.2.106