List of variants reported as likely pathogenic for autosomal dominant non-syndromic intellectual disability by Service de Génétique Moléculaire, Hôpital Robert Debré

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001321075.3(DLG4):c.210+2del
NM_001374828.1(ARID1B):c.3581_3602del (p.Leu1194fs)	rs1792478147
NM_004859.4(CLTC):c.3611del (p.Arg1204fs)
NM_006015.6(ARID1A):c.3198+2dup
NM_015981.4(CAMK2A):c.220C>T (p.Arg74Ter)
NM_019842.4(KCNQ5):c.875A>G (p.Asn292Ser)
NM_057175.5(NAA15):c.55-2A>C
NM_205768.3(ZBTB18):c.244_246dup (p.Pro82_Ala83insPro)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.