CELSR2 c.3311-2333G>A

Variant ID: 1-109798721-G-A

NM_001408.2(CELSR2):c.3311-2333G>A

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:

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.

Plos One
Einarsdottir, Elisabet E; Grauers, Anna A; Wang, Jingwen J; Jiao, Hong H; Escher, Stefan A SA; Danielsson, Aina A; Simony, Ane A; Andersen, Mikkel M; Christensen, Steen Bach SB; Åkesson, Kristina K; Kou, Ikuyo I; Khanshour, Anas M AM; Ohlin, Acke A; Wise, Carol C; Ikegawa, Shiro S; Kere, Juha J; Gerdhem, Paul P
Publication Date: 2017

Variant appearance in text: rs10858082
PubMed Link: 29240829
Variant Present in the following documents:
  • Main text
  • pone.0189591.pdf
View BVdb publication page