KMT2D c.10231+814G>A

Variant ID: 12-49430094-C-T

NM_003482.3(KMT2D):c.10231+814G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


An integrative analysis of genome-wide association study and regulatory SNP annotation datasets identified candidate genes for bipolar disorder.

International Journal Of Bipolar Disorders
Qi, Xin X; Wen, Yan Y; Li, Ping P; Liang, Chujun C; Cheng, Bolun B; Ma, Mei M; Cheng, Shiqiang S; Zhang, Lu L; Liu, Li L; Kafle, Om Prakash OP; Zhang, Feng F
Publication Date: 2020-02-03

Variant appearance in text: rs10875915
PubMed Link: 32009227
Variant Present in the following documents:
  • Main text
  • 40345_2019_Article_170.pdf
View BVdb publication page



CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.

Journal Of Neuro-Oncology
Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B
Publication Date: 2015-10

Variant appearance in text: rs10875915
PubMed Link: 26290144
Variant Present in the following documents:
  • 11060_2015_1891_MOESM1_ESM.pdf
View BVdb publication page