CUBN c.8906-2274A>G

Variant ID: 10-16921370-T-C

NM_001081.3(CUBN):c.8906-2274A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia.

Journal Of Medical Genetics
Guo, Hui H; Jin, Xuemin X; Zhu, Tengfei T; Wang, Tianyun T; Tong, Ping P; Tian, Lei L; Peng, Yu Y; Sun, Liangdan L; Wan, Anran A; Chen, Jingjing J; Liu, Yanling Y; Li, Ying Y; Tian, Qi Q; Xia, Lu L; Zhang, Lusi L; Pan, Yongcheng Y; Lu, Lina L; Liu, Qiong Q; Shen, Lu L; Li, Yunping Y; Xiong, Wei W; Li, Jiada J; Tang, Beisha B; Feng, Yong Y; Zhang, Xuejun X; Zhang, Zhuohua Z; Pan, Qian Q; Hu, Zhengmao Z; Xia, Kun K
Publication Date: 2014-08

Variant appearance in text: rs780838
PubMed Link: 24891338
Variant Present in the following documents:
  • jmedgenet-2014-102351-s1.pdf
View BVdb publication page



A genome-wide tree- and forest-based association analysis of comorbidity of alcoholism and smoking.

Bmc Genetics
Ye, Yuanqing Y; Zhong, Xiaoyun X; Zhang, Heping H
Publication Date: 2005-12-30

Variant appearance in text: rs780838
PubMed Link: 16451594
Variant Present in the following documents:
  • Main text
  • 1471-2156-6-S1-S135.pdf
View BVdb publication page