GRIN2A c.414+84956C>G

Variant ID: 16-10188899-G-C

NM_001134407.1(GRIN2A):c.414+84956C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach.

Psychoneuroendocrinology
Velders, Fleur P FP; Kuningas, Maris M; Kumari, Meena M; Dekker, Marieke J MJ; Uitterlinden, Andre G AG; Kirschbaum, Clemens C; Hek, Karin K; Hofman, Albert A; Verhulst, Frank C FC; Kivimaki, Mika M; Van Duijn, Cornelia M CM; Walker, Brian R BR; Tiemeier, Henning H
Publication Date: 2011-08

Variant appearance in text: rs8062512
PubMed Link: 21316860
Variant Present in the following documents:
  • Main text
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