EHMT2 c.583-454T>A

Variant ID: 6-31861141-A-T

NM_006709.3(EHMT2):c.583-454T>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Fine-mapping of HLA class I and class II genes identified two independent novel variants associated with nasopharyngeal carcinoma susceptibility.

Cancer Medicine
Wang, Tong-Min TM; Zhou, Ting T; He, Yong-Qiao YQ; Xue, Wen-Qiong WQ; Zhang, Jiang-Bo JB; Zheng, Xiao-Hui XH; Li, Xi-Zhao XZ; Zhang, Shao-Dan SD; Zeng, Yi-Xin YX; Jia, Wei-Hua WH
Publication Date: 2018-12

Variant appearance in text: rs2844457
PubMed Link: 30378292
Variant Present in the following documents:
  • CAM4-7-6308-s006.xlsx, sheet 1
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2844457
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Leveraging existing data sets to generate new insights into Alzheimer's disease biology in specific patient subsets.

Scientific Reports
Fowler, Kevin D KD; Funt, Jason M JM; Artyomov, Maxim N MN; Zeskind, Benjamin B; Kolitz, Sarah E SE; Towfic, Fadi F
Publication Date: 2015-09-23

Variant appearance in text: rs2844457
PubMed Link: 26395074
Variant Present in the following documents:
  • srep14324-s1.pdf
View BVdb publication page