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ANGPT2 c.289-1294T>C
Variant ID: 8-6391302-A-G
NM_001118887.1(
ANGPT2
):c.289-1294T>C
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: rs2959812
PubMed Link:
29312345
Variant Present in the following documents:
Main text
fimmu-08-01868.pdf
View BVdb publication page