ANGPT2 c.445-642A>T

Variant ID: 8-6385839-T-A

NM_001118887.1(ANGPT2):c.445-642A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity.

Frontiers In Immunology
Rathi, Sonika S; Jalali, Subhadra S; Patnaik, Satish S; Shahulhameed, Shahna S; Musada, Ganeswara R GR; Balakrishnan, Divya D; Rani, Padmaja K PK; Kekunnaya, Ramesh R; Chhablani, Preeti Patil PP; Swain, Sarpras S; Giri, Lopamudra L; Chakrabarti, Subhabrata S; Kaur, Inderjeet I
Publication Date: 2017

Variant appearance in text: rs2515464
PubMed Link: 29312345
Variant Present in the following documents:
  • Main text
  • fimmu-08-01868.pdf
View BVdb publication page



Microcephaly genes and risk of late-onset Alzheimer disease.

Alzheimer Disease And Associated Disorders
Erten-Lyons, Deniz D; Wilmot, Beth B; Anur, Pavana P; McWeeney, Shannon S; Westaway, Shawn K SK; Silbert, Lisa L; Kramer, Patricia P; Kaye, Jeffrey J
Publication Date: 2011

Variant appearance in text: rs2515464
PubMed Link: 21297427
Variant Present in the following documents:
  • Main text
View BVdb publication page