<p>Only healthy control participants of the replication studies that were fully genotyped at all 7 loci were used in this analysis. Similar to the GWAS study, the risk score distributions were significantly different by ethnicity (ANOVA p = 2.1×10<sup>−38</sup>). The corresponding differences in the distribution of risk alleles are depicted in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002765#pgen.1002765.s001" target="_blank">Figure S1</a>.</p
Abstract Background Accurate assessment of health disparities requires unbiased knowledge of genetic...
<p>Bold-faced values indicate significant difference.</p>*<p>Two-sided χ<sup>2</sup> test for the di...
<div><p>Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele ...
<div><p>The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thu...
The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thus unders...
The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thus unders...
<p>Distribution of the seven SNPs-based genetic risk score in 1,387 NPC cases (black bars) and 1,459...
The last several years have seen strong evidence that common genetic variants can together explain a...
The majority of polygenic risk scores (PRSs) have been developed and optimized in individuals of Eur...
<p>Eleven independent cross-ethnic T2D risk alleles were combined as an ensemble to calculate the av...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
Polygenic scores (PGS) have been widely used to predict disease risk using variants identified from ...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<p>Frequencies of the risk allele of 1p11-rs11249433 polymorphism among controls stratified by ethnic...
Genetic variants that contribute to risk of common disease may differ in frequency across population...
Abstract Background Accurate assessment of health disparities requires unbiased knowledge of genetic...
<p>Bold-faced values indicate significant difference.</p>*<p>Two-sided χ<sup>2</sup> test for the di...
<div><p>Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele ...
<div><p>The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thu...
The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thus unders...
The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thus unders...
<p>Distribution of the seven SNPs-based genetic risk score in 1,387 NPC cases (black bars) and 1,459...
The last several years have seen strong evidence that common genetic variants can together explain a...
The majority of polygenic risk scores (PRSs) have been developed and optimized in individuals of Eur...
<p>Eleven independent cross-ethnic T2D risk alleles were combined as an ensemble to calculate the av...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
Polygenic scores (PGS) have been widely used to predict disease risk using variants identified from ...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<p>Frequencies of the risk allele of 1p11-rs11249433 polymorphism among controls stratified by ethnic...
Genetic variants that contribute to risk of common disease may differ in frequency across population...
Abstract Background Accurate assessment of health disparities requires unbiased knowledge of genetic...
<p>Bold-faced values indicate significant difference.</p>*<p>Two-sided χ<sup>2</sup> test for the di...
<div><p>Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele ...