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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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