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DMD c.3786+2T>A
Variant ID: X-32466571-A-T
NM_004006.2(
DMD
):c.3786+2T>A
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:
Haplotype-Based Noninvasive Prenatal Diagnosis of 21 Families With Duchenne Muscular Dystrophy: Real-World Clinical Data in China.
Frontiers In Genetics
Kong, Lingrong L; Li, Shaojun S; Zhao, Zhenhua Z; Feng, Jun J; Chen, Guangquan G; Liu, Lina L; Tang, Weiqin W; Li, Suqing S; Li, Feifei F; Han, Xiujuan X; Wu, Di D; Zhang, Haichuan H; Sun, Luming L; Kong, Xiangdong X
Publication Date: 2021
Variant appearance in text: DMD: 3786+2T>A
PubMed Link:
34970304
Variant Present in the following documents:
Main text
fgene-12-791856.pdf
View BVdb publication page