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VWF c.6446A>G ;(p.E2149G)
Variant ID: 12-6103180-T-C
NM_000552.3(
VWF
):c.6446A>G;(p.E2149G)
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:
Molecular classification of blood and bleeding disorder genes.
Npj Genomic Medicine
Baz, Batoul B; Abouelhoda, Mohamed M; Owaidah, Tarek T; Dasouki, Majed M; Monies, Dorota D; Al Tassan, Nada N
Publication Date: 2021-07-16
Variant appearance in text: VWF: 6446A>G; Glu2149Gly
PubMed Link:
34272389
Variant Present in the following documents:
41525_2021_228_MOESM1_ESM.pdf
View BVdb publication page