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
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HGVS dbSNP
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

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