ClinVar Miner

List of variants in gene ARHGEF9 reported as likely benign for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_015185.2(ARHGEF9):c.562-8dup rs782366734
NM_015185.3(ARHGEF9):c.1204A>G (p.Ile402Val) rs56110425
NM_015185.3(ARHGEF9):c.1272G>A (p.Arg424=) rs782387990
NM_015185.3(ARHGEF9):c.1467G>A (p.Ser489=) rs782580975
NM_015185.3(ARHGEF9):c.243C>T (p.Asn81=) rs782671712
NM_015185.3(ARHGEF9):c.28A>G (p.Ile10Val) rs55868891
NM_015185.3(ARHGEF9):c.330G>A (p.Glu110=) rs373866956
NM_015185.3(ARHGEF9):c.351C>T (p.His117=) rs138198839
NM_015185.3(ARHGEF9):c.543A>G (p.Gly181=) rs782187939
NM_015185.3(ARHGEF9):c.794+8A>G rs1464003224
NM_015185.3(ARHGEF9):c.794+8A>T rs1464003224

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.