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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3736321

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

A search for variants in coding exons of 25 genome-wide association study risk genes in a large cohort of autoimmune patients finds that rare coding-region variants at known loci have a negligible role in common autoimmune disease susceptibility, arguing against the previously proposed rare-variant synthetic genome-wide association hypothesis.
I...

Alternative Titles

Full title

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3736321

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3736321

Other Identifiers

ISSN

0028-0836

E-ISSN

1476-4687

DOI

10.1038/nature12170

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