§§<p>The subjects from Surolia et al. (4) and Hirschfield et al. (5) include controls and autoimmune subjects of European ancestry. EVS (Exome variant server) data comprises unannotated American subjects (disease status is unknown) of European and African ancestry and is current as of June 20th 2012. Rare variants reported in both African-Americans and European-Americans are marked with a single asterisk (*n = 6500). Rare variants seen only in European-Americans or only in African-Americans are marked with double (**n = 4299) and triple asterisks (***n = 2201) respectively.</p>nf<p>These variants were found in dbSNP and/or 1000 genomes project but frequency data is not available. The dbSNP data is not ethnically stratified and was derived f...
The number and distribution of recessive alleles in the population for various diseases are not know...
<p>*MAF<5% in at least one pool.</p><p>EA = European American, AA = African American, MAF = minor al...
<div><p>Exome sequencing has revealed the causative mutations behind numerous rare, inherited disord...
§<p>The subjects from Surolia et al. (4) include controls and autoimmune subjects of European ancest...
Genome-wide association studies have uncovered thousands of common variants associated with human di...
Recent studies have shown that a high proportion of rare variants in European and African population...
Recommendations for laboratories to report incidental findings from genomic tests have stimulated in...
<p>NA: DNA not available from relatives. IP: Incomplete penetrance. CM: Human gene variation databas...
Rare exome variants identified in affected individuals from the investigated Cuban pedigrees.</p
The incorporation of genomics into medicine is stimulating interest on the return of incidental find...
<p>Minor allele frequencies of four nonsynonymous variants associated with asthma following severe R...
For recent advancements in sequencing technologies, genetic information can be obtained from a large...
Somatic mutations are an inevitable component of ageing and the most important cause of cancer. The ...
Genome-wide association studies (GWAS) have successfully described the roles of common genetic varia...
<p>A) In average around 230 variants pass the filter in CEU exomes and 309 in YRI exomes. B) The pot...
The number and distribution of recessive alleles in the population for various diseases are not know...
<p>*MAF<5% in at least one pool.</p><p>EA = European American, AA = African American, MAF = minor al...
<div><p>Exome sequencing has revealed the causative mutations behind numerous rare, inherited disord...
§<p>The subjects from Surolia et al. (4) include controls and autoimmune subjects of European ancest...
Genome-wide association studies have uncovered thousands of common variants associated with human di...
Recent studies have shown that a high proportion of rare variants in European and African population...
Recommendations for laboratories to report incidental findings from genomic tests have stimulated in...
<p>NA: DNA not available from relatives. IP: Incomplete penetrance. CM: Human gene variation databas...
Rare exome variants identified in affected individuals from the investigated Cuban pedigrees.</p
The incorporation of genomics into medicine is stimulating interest on the return of incidental find...
<p>Minor allele frequencies of four nonsynonymous variants associated with asthma following severe R...
For recent advancements in sequencing technologies, genetic information can be obtained from a large...
Somatic mutations are an inevitable component of ageing and the most important cause of cancer. The ...
Genome-wide association studies (GWAS) have successfully described the roles of common genetic varia...
<p>A) In average around 230 variants pass the filter in CEU exomes and 309 in YRI exomes. B) The pot...
The number and distribution of recessive alleles in the population for various diseases are not know...
<p>*MAF<5% in at least one pool.</p><p>EA = European American, AA = African American, MAF = minor al...
<div><p>Exome sequencing has revealed the causative mutations behind numerous rare, inherited disord...