QTRT1 c.451+434T>C

Variant ID: 19-10813364-T-C

NM_031209.2(QTRT1):c.451+434T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese.

National Science Review
Yao, Kang K; Dai, Yuxiang Y; Shen, Juan J; Wang, Yi Y; Yang, Huanjie H; Wu, Runda R; Liao, Qijun Q; Wu, Hongyi H; Fang, Xiaodong X; Shali, Shalaimaiti S; Xu, Lili L; Hao, Meng M; Lin, Chenhao C; Sun, Zhonghan Z; Liu, Yilian Y; Li, Mengxin M; Wang, Zhen Z; Gao, Qiang Q; Zhang, Shuning S; Li, Chenguang C; Gao, Wei W; Ge, Lei L; Zou, Yunzeng Y; Sun, Aijun A; Qian, Juying J; Jin, Li L; Hong, Shangyu S; Zheng, Yan Y; Ge, Junbo J
Publication Date: 2022-08

Variant appearance in text: rs4425006
PubMed Link: 36060302
Variant Present in the following documents:
  • Main text
  • nwac102.pdf
View BVdb publication page



Genetic association of recovery from eating disorders: the role of GABA receptor SNPs.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Bloss, Cinnamon S CS; Berrettini, Wade W; Bergen, Andrew W AW; Magistretti, Pierre P; Duvvuri, Vikas V; Strober, Michael M; Brandt, Harry H; Crawford, Steve S; Crow, Scott S; Fichter, Manfred M MM; Halmi, Katherine A KA; Johnson, Craig C; Kaplan, Allan S AS; Keel, Pamela P; Klump, Kelly L KL; Mitchell, James J; Treasure, Janet J; Woodside, D Blake DB; Marzola, Enrica E; Schork, Nicholas J NJ; Kaye, Walter H WH
Publication Date: 2011-10

Variant appearance in text: rs4425006
PubMed Link: 21750581
Variant Present in the following documents:
  • Main text
View BVdb publication page