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VWF c.1173A>C ;(p.T391=)
Variant ID: 12-6174423-T-G
NM_000552.3(
VWF
):c.1173A>C;(p.T391=)
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:
Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
The Indian Journal Of Medical Research
Kasatkar, Priyanka P; Ghosh, Kanjaksha K; Shetty, Shrimati S
Publication Date: 2015-12
Variant appearance in text: VWF: T391T
PubMed Link:
26831425
Variant Present in the following documents:
Main text
View BVdb publication page