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VWF c.1909G>C ;(p.G637R)
Variant ID: 12-6166059-C-G
NM_000552.3(
VWF
):c.1909G>C;(p.G637R)
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:
Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy.
Journal Of Molecular Medicine (Berlin, Germany)
Haydock, Ludwig L; Garneau, Alexandre P AP; Tremblay, Laurence L; Yen, Hai-Yun HY; Gao, Hanlin H; Harrisson, Raphaƫl R; Isenring, Paul P
Publication Date: 2022-02
Variant appearance in text: VWF: Gly637Arg
PubMed Link:
34714369
Variant Present in the following documents:
109_2021_Article_2102.pdf
View BVdb publication page