GRIN2A c.2169-7736A>G

Variant ID: 16-9900057-T-C

NM_001134407.1(GRIN2A):c.2169-7736A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.

Nature Neuroscience
Liang, Dan D; Elwell, Angela L AL; Aygün, Nil N; Krupa, Oleh O; Wolter, Justin M JM; Kyere, Felix A FA; Lafferty, Michael J MJ; Cheek, Kerry E KE; Courtney, Kenan P KP; Yusupova, Marianna M; Garrett, Melanie E ME; Ashley-Koch, Allison A; Crawford, Gregory E GE; Love, Michael I MI; de la Torre-Ubieta, Luis L; Geschwind, Daniel H DH; Stein, Jason L JL
Publication Date: 2021-07

Variant appearance in text: rs7191183
PubMed Link: 34017130
Variant Present in the following documents:
  • Main text
  • nihms-1694740.pdf
View BVdb publication page



OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individuals.

Molecular Psychiatry
Ehrenreich, H H; Mitjans, M M; Van der Auwera, S S; Centeno, T P TP; Begemann, M M; Grabe, H J HJ; Bonn, S S; Nave, K-A KA
Publication Date: 2018-02

Variant appearance in text: rs7191183
PubMed Link: 27922606
Variant Present in the following documents:
  • Main text
  • mp2016208a.pdf
View BVdb publication page