FBN1 c.4639A>G ;(p.T1547A)

Variant ID: 15-48760243-T-C

NM_000138.4(FBN1):c.4639A>G;(p.T1547A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare Variants and Polymorphisms of FBN1 Gene May Increase the Risk of Non-Syndromic Aortic Dissection.

Frontiers In Genetics
Pan, Meichen M; Li, Lianjie L; Li, Zehao Z; Chen, Shu S; Li, Zongzhe Z; Wang, Yuning Y; He, Henghui H; Lin, Lihua L; Wang, Haihao H; Liu, Qian Q
Publication Date: 2022

Variant appearance in text: FBN1: 4639A>G; Thr1547Ala
PubMed Link: 35154271
Variant Present in the following documents:
  • Main text
  • fgene-13-778806.pdf
View BVdb publication page