RELN c.337+11114T>C

Variant ID: 7-103546408-A-G

NM_005045.3(RELN):c.337+11114T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.

American Journal Of Human Genetics
Schrauwen, Isabelle I; Ealy, Megan M; Huentelman, Matthew J MJ; Thys, Melissa M; Homer, Nils N; Vanderstraeten, Kathleen K; Fransen, Erik E; Corneveaux, Jason J JJ; Craig, David W DW; Claustres, Mireille M; Cremers, Cor W R J CW; Dhooge, Ingeborg I; Van de Heyning, Paul P; Vincent, Robert R; Offeciers, Erwin E; Smith, Richard J H RJ; Van Camp, Guy G
Publication Date: 2009-03

Variant appearance in text: rs802786
PubMed Link: 19230858
Variant Present in the following documents:
  • Main text
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