Bibliome.ai browser hg19
Search
About
Stats
FAQ
VWF c.2208G>T ;(p.M736I)
Variant ID: 12-6155962-C-A
NM_000552.3(
VWF
):c.2208G>T;(p.M736I)
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 heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients.
Plos One
Kasatkar, Priyanka P; Shetty, Shrimati S; Ghosh, Kanjaksha K
Publication Date: 2014
Variant appearance in text: VWF: 2208G>T; M736I
PubMed Link:
24675615
Variant Present in the following documents:
Main text
pone.0092575.pdf
View BVdb publication page