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Paper Details

Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital.
Pac Symp Biocomput
1
2020
APOL1, APOL1 renal risk alleles, APOL1 renal risk variants, CKD, Chronic Kidney Disease, ClinVar Pathogenic Variants, ClinVar variants, ClinVar-designated variants, FTA, G1, G2, Patients, TTR rs76992529, allele, amyloidogenic transthyretin amyloidosis, autosomal dominant disorder, autosomal recessive disorders, chronic kidney disease, familial transthyretin amyloidosis, participant, participants, patients, renal risk allele, renal risk alleles, rs71785313, rs73885319, rs76992529
Author NameAffiliation
Dana C CrawfordCleveland Institute for Computational Biology, Case Western Reserve University
Dana C CrawfordCase Western Reserve University
Dana C CrawfordCase Western Reserve University
Dana C CrawfordCleveland Institute for Computational Biology, Case Western Reserve University
Dana C CrawfordCase Western Reserve University
Dana C CrawfordCase Western Reserve University
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink