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FBN1 c.3337+103C>T
Variant ID: 15-48780207-G-A
NM_000138.4(
FBN1
):c.3337+103C>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Rare Causes of Arterial Hypertension and Thoracic Aortic Aneurysms-A Case-Based Review.
Diagnostics (Basel, Switzerland)
Encica, Svetlana S; Molnar, Adrian A; Manole, Simona S; Filan, Teodora T; Oprița, Simona S; Bursașiu, Eugen E; Vulturar, Romana R; Damian, Laura L
Publication Date: 2021-03-05
Variant appearance in text: rs11856553
PubMed Link:
33807627
Variant Present in the following documents:
Main text
diagnostics-11-00446.pdf
View BVdb publication page
Advances in the Genetics of Hypertension: The Effect of Rare Variants.
International Journal Of Molecular Sciences
Russo, Alessia A; Di Gaetano, Cornelia C; Cugliari, Giovanni G; Matullo, Giuseppe G
Publication Date: 2018-02-28
Variant appearance in text: rs11856553
PubMed Link:
29495593
Variant Present in the following documents:
Main text
ijms-19-00688.pdf
View BVdb publication page