จากการวิเคราะห์ SNP ที่มีความเสี่ยง

จากการวิเคราะห์ SNP ที่มีความเสี่ยงต่อการเกิดโรคโดยการเทียบ SNP ของคน Thai กับ variants from genome-wide association data, We found the Thai genome carries 23 variations significantly of disease risk และพบว่ามีเพียง 11 variations เท่านั้น ที่มี risk allele ทำให้เสี่ยงต่อการเกิดโรคดังต่อไปนี้

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Snp analysis of the risk of the disease by comparing snp thai with variants from genome-wide association data,.we found the thai genome carries 23 variations significantly of disease risk and found that only 11 variations, only the risk allele increased risk of disease follows.

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From the analysis of the SNP risk disease by equating SNP of Thai with variants from genome-wide, association dataWe found the Thai genome carries 23 variations significantly of disease risk and found that only 11 variations only Risk allele makes high risk following

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The SNP analysis of the risk of disease by comparing a person's SNP variants from the Thai genome-wide association data, We found the Thai genome variations of disease risk significantly 23 carries and found that only 11 variations only with risk allele causes a risk of the disease is as follows:

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