CDYL2 c.24+19371A>G

Variant ID: 16-80818676-T-C

NM_152342.2(CDYL2):c.24+19371A>G

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: rs17761499
PubMed Link: 19230858
Variant Present in the following documents:
  • Main text
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