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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.
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: rs11065851
PubMed Link:
30382898
Variant Present in the following documents:
Main text
View BVdb publication page