VIL1 c.567+266C>T

Variant ID: 2-219293326-C-T

NM_007127.2(VIL1):c.567+266C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


CINOEDV: a co-information based method for detecting and visualizing n-order epistatic interactions.

Bmc Bioinformatics
Shang, Junliang J; Sun, Yingxia Y; Liu, Jin-Xing JX; Xia, Junfeng J; Zhang, Junying J; Zheng, Chun-Hou CH
Publication Date: 2016-05-17

Variant appearance in text: rs4674305
PubMed Link: 27184783
Variant Present in the following documents:
  • 12859_2016_1076_MOESM1_ESM.pdf
View BVdb publication page



Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

American Journal Of Human Genetics
Adaimy, Lynn L; Chouery, Eliane E; Megarbane, Hala H; Mroueh, Salman S; Delague, Valerie V; Nicolas, Elsa E; Belguith, Hanen H; de Mazancourt, Philippe P; Megarbane, Andre A
Publication Date: 2007-10

Variant appearance in text: rs4674305
PubMed Link: 17847007
Variant Present in the following documents:
  • Main text
View BVdb publication page