VWF c.6799-1845C>T

Variant ID: 12-6096676-G-A

NM_000552.3(VWF):c.6799-1845C>T

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:

In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion.

Haemophilia : The Official Journal Of The World Federation Of Hemophilia
Cartwright, A A; Peake, I R IR; Goodeve, A C AC; Hampshire, D J DJ
Publication Date: 2016-09

Variant appearance in text: VWF: 6799-1845C>T; rs526881
PubMed Link: 27481636
Variant Present in the following documents:
  • Main text
View BVdb publication page