CUX2 c.64-41281T>A

Variant ID: 12-111610723-T-A

NM_015267.3(CUX2):c.64-41281T>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:

Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics
Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J
Publication Date: 2018-11-01

Variant appearance in text: rs16941284
PubMed Link: 30382898
Variant Present in the following documents:
  • Main text
View BVdb publication page