VWF c.1728G>C ;(p.M576I)

Variant ID: 12-6167016-C-G

NM_000552.3(VWF):c.1728G>C;(p.M576I)

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:

Characterizing polymorphisms and allelic diversity of von Willebrand factor gene in the 1000 Genomes.

Journal Of Thrombosis And Haemostasis : Jth
Wang, Q Y QY; Song, J J; Gibbs, R A RA; Boerwinkle, E E; Dong, J F JF; Yu, F L FL
Publication Date: 2013-02

Variant appearance in text: VWF: M576I
PubMed Link: 23216583
Variant Present in the following documents:
  • Main text
View BVdb publication page