CUX2 c.302-5483G>A

Variant ID: 12-111723739-G-A

NM_015267.3(CUX2):c.302-5483G>A

This variant was identified in 1 publication

View GRCh38 version.




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: rs11065851
PubMed Link: 30382898
Variant Present in the following documents:
  • Main text
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