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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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