KDM5B c.205-14436A>G

Variant ID: 1-202760658-T-C

NM_006618.3(KDM5B):c.205-14436A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Model-based clustering for identifying disease-associated SNPs in case-control genome-wide association studies.

Scientific Reports
Xu, Yan Y; Xing, Li L; Su, Jessica J; Zhang, Xuekui X; Qiu, Weiliang W
Publication Date: 2019-09-23

Variant appearance in text: rs4351714
PubMed Link: 31548641
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_50229.pdf
View BVdb publication page



Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.

Molecular Genetics & Genomic Medicine
Wight, Jenny E JE; Nguyen, Viet-Huong VH; Medina, Marco T MT; Patterson, Christopher C; Durón, Reyna M RM; Molina, Yolly Y; Lin, Yu-Chen YC; Martínez-Juárez, Iris E IE; Ochoa, Adriana A; Jara-Prado, Aurelio A; Tanaka, Miyabi M; Bai, Dongsheng D; Aftab, Sumaya S; Bailey, Julia N JN; Delgado-Escueta, Antonio V AV
Publication Date: 2016-03

Variant appearance in text: rs4351714
PubMed Link: 27066514
Variant Present in the following documents:
  • Main text
  • MGG3-4-197.pdf
View BVdb publication page