GSTM1 c.361-92A>G

Variant ID: 1-110232801-A-G

NM_000561.3(GSTM1):c.361-92A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role.

European Journal Of Pediatrics
Luo, Xi X; Zhao, Min M; Chen, Cheng C; Lin, Fengji F; Li, Xiaodong X; Huang, Haiyun H; Dou, Lei L; Feng, Jinxing J; Xiao, Shanqiu S; Liu, Dong D; He, Junli J; Yu, Jialin J
Publication Date: 2023-02-09

Variant appearance in text: rs756637
PubMed Link: 36757497
Variant Present in the following documents:
  • 431_2022_4779_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: GSTM1: 361-92A>G; rs756637
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs756637
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page