VWF c.7437+1086C>A

Variant ID: 12-6084191-G-T

NM_000552.3(VWF):c.7437+1086C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.

Human Genetics
Mukhopadhyay, Nandita N; Bishop, Madison M; Mortillo, Michael M; Chopra, Pankaj P; Hetmanski, Jacqueline B JB; Taub, Margaret A MA; Moreno, Lina M LM; Valencia-Ramirez, Luz Consuelo LC; Restrepo, Claudia C; Wehby, George L GL; Hecht, Jacqueline T JT; Deleyiannis, Frederic F; Butali, Azeez A; Weinberg, Seth M SM; Beaty, Terri H TH; Murray, Jeffrey C JC; Leslie, Elizabeth J EJ; Feingold, Eleanor E; Marazita, Mary L ML
Publication Date: 2020-02

Variant appearance in text: rs216852
PubMed Link: 31848685
Variant Present in the following documents:
  • Main text
  • 439_2019_Article_2099.pdf
View BVdb publication page



Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence.

Plos One
Johnson, Catherine C; Drgon, Tomas T; Walther, Donna D; Uhl, George R GR
Publication Date: 2011

Variant appearance in text: rs216852
PubMed Link: 21818250
Variant Present in the following documents:
  • Main text
View BVdb publication page