DMD c.4071+2012T>G

Variant ID: X-32454346-A-C

NM_004006.2(DMD):c.4071+2012T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.

Frontiers In Genetics
Skare, Øivind Ø; Lie, Rolv T RT; Haaland, Øystein A ØA; Gjerdevik, Miriam M; Romanowska, Julia J; Gjessing, Håkon K HK; Jugessur, Astanand A
Publication Date: 2018

Variant appearance in text: rs2405829
PubMed Link: 29520293
Variant Present in the following documents:
  • Main text
  • fgene-09-00025.pdf
View BVdb publication page



Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.

Molecular Psychiatry
Shyn, S I SI; Shi, J J; Kraft, J B JB; Potash, J B JB; Knowles, J A JA; Weissman, M M MM; Garriock, H A HA; Yokoyama, J S JS; McGrath, P J PJ; Peters, E J EJ; Scheftner, W A WA; Coryell, W W; Lawson, W B WB; Jancic, D D; Gejman, P V PV; Sanders, A R AR; Holmans, P P; Slager, S L SL; Levinson, D F DF; Hamilton, S P SP
Publication Date: 2011-02

Variant appearance in text: rs2405829
PubMed Link: 20038947
Variant Present in the following documents:
  • Main text
  • NIHMS142361-supplement-1.pdf
View BVdb publication page