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Disease table of EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
OMIM ID: 612269
Gene-disease associations table
Gene
Associated with EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 in
Link to HGNC
Cytogenetic band
Number of associated diseases
Associated diseases
GABRB3
ClinVar, OMIM, HUMSAVAR
HGNC link
15q12
1
612269
Download the disease annotation in CSV format