BDNF c.569G>T ;(p.G190V)

Variant ID: 11-27679543-C-A

NM_001709.4(BDNF):c.569G>T;(p.G190V)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Rare variants in the neurotrophin signaling pathway implicated in schizophrenia risk.

Schizophrenia Research
Kranz, Thorsten M TM; Goetz, Ray R RR; Walsh-Messinger, Julie J; Goetz, Deborah D; Antonius, Daniel D; Dolgalev, Igor I; Heguy, Adriana A; Seandel, Marco M; Malaspina, Dolores D; Chao, Moses V MV
Publication Date: 2015-10

Variant appearance in text: BDNF: G190V
PubMed Link: 26215504
Variant Present in the following documents:
  • Main text
View BVdb publication page