TMEM106B c.-3+739G>C

Variant ID: 7-12251790-G-C

NM_001134232.2(TMEM106B):c.-3+739G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression.

American Journal Of Human Genetics
Gallagher, Michael D MD; Posavi, Marijan M; Huang, Peng P; Unger, Travis L TL; Berlyand, Yosef Y; Gruenewald, Analise L AL; Chesi, Alessandra A; Manduchi, Elisabetta E; Wells, Andrew D AD; Grant, Struan F A SFA; Blobel, Gerd A GA; Brown, Christopher D CD; Chen-Plotkin, Alice S AS
Publication Date: 2017-11-02

Variant appearance in text: rs1019307
PubMed Link: 29056226
Variant Present in the following documents:
  • Main text
View BVdb publication page