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SLC1A1 c.91+2756T>G
Variant ID: 9-4493526-T-G
NM_004170.5(
SLC1A1
):c.91+2756T>G
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:
Solute Carrier Family 1 (SLC1A1) Contributes to Susceptibility and Psychopathology Symptoms of Schizophrenia in the Han Chinese Population.
Frontiers In Psychiatry
Li, Wenqiang W; Su, Xi X; Chen, Tengfei T; Li, Zhen Z; Yang, Yongfeng Y; Zhang, Luwen L; Liu, Qing Q; Shao, Minglong M; Zhang, Yan Y; Ding, Minli M; Lu, Yanli Y; Yu, Hongyan H; Fan, Xiaoduo X; Song, Meng M; Lv, Luxian L
Publication Date: 2020
Variant appearance in text: rs7045401
PubMed Link:
33173509
Variant Present in the following documents:
Main text
fpsyt-11-559210.pdf
View BVdb publication page