DNAH17 c.6818+1120T>C

Variant ID: 17-76485661-A-G

NM_173628.3(DNAH17):c.6818+1120T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Doyle, Alysa E AE; Ferreira, Manuel A R MA; Sklar, Pamela B PB; Lasky-Su, Jessica J; Petty, Carter C; Fusillo, Steven J SJ; Seidman, Larry J LJ; Willcutt, Erik G EG; Smoller, Jordan W JW; Purcell, Shaun S; Biederman, Joseph J; Faraone, Stephen V SV
Publication Date: 2008-12-05

Variant appearance in text: rs894976
PubMed Link: 18973233
Variant Present in the following documents:
  • Main text
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