RNF130 c.848+828C>T

Variant ID: 5-179404375-G-A

NM_018434.5(RNF130):c.848+828C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.

European Journal Of Human Genetics : Ejhg
Dusatkova, Petra P; Pfäffle, Roland R; Brown, Milton R MR; Akulevich, Natallia N; Arnhold, Ivo J P IJ; Kalina, Maria A MA; Kot, Karolina K; Krzisnik, Ciril C; Lemos, Manuel C MC; Malikova, Jana J; Navardauskaite, Ruta R; Obermannova, Barbora B; Pribilincova, Zuzana Z; Sallai, Agnes A; Stipancic, Gordana G; Verkauskiene, Rasa R; Cinek, Ondrej O; Blum, Werner F WF; Parks, John S JS; Austerlitz, Frederic F; Lebl, Jan J
Publication Date: 2016-03

Variant appearance in text: rs27017
PubMed Link: 26059845
Variant Present in the following documents:
  • Main text
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