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GNB1L c.732+1788G>A
Variant ID: 22-19787736-C-T
NM_053004.2(
GNB1L
):c.732+1788G>A
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:
Supportive evidence for reduced expression of GNB1L in schizophrenia.
Schizophrenia Bulletin
Ishiguro, Hiroki H; Koga, Minori M; Horiuchi, Yasue Y; Noguchi, Emiko E; Morikawa, Miyuki M; Suzuki, Yoshimi Y; Arai, Makoto M; Niizato, Kazuhiro K; Iritani, Shyuji S; Itokawa, Masanari M; Inada, Toshiya T; Iwata, Nakao N; Ozaki, Norio N; Ujike, Hiroshi H; Kunugi, Hiroshi H; Sasaki, Tsukasa T; Takahashi, Makoto M; Watanabe, Yuichiro Y; Someya, Toshiyuki T; Kakita, Akiyoshi A; Takahashi, Hitoshi H; Nawa, Hiroyuki H; Arinami, Tadao T
Publication Date: 2010-07
Variant appearance in text: rs748806
PubMed Link:
19011233
Variant Present in the following documents:
Main text
View BVdb publication page